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Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


1

Ionic liquid ion source emitter arrays fabricated on bulk porous substrates for spacecraft propulsion  

E-Print Network [OSTI]

Ionic Liquid Ion Sources (ILIS) are a subset of electrospray capable of producing bipolar beams of pure ions from ionic liquids. Ionic liquids are room temperature molten salts, characterized by negligible vapor pressures, ...

Courtney, Daniel George

2011-01-01T23:59:59.000Z

2

Synthesis of ionic liquids  

DOE Patents [OSTI]

Ionic compounds which are liquids at room temperature are formed by the method of mixing a neutral organic liqand with the salt of a metal cation and its conjugate anion. The liquids are hydrophobic, conductive and stable and have uses as solvents and in electrochemical devices.

Dai, Sheng [Knoxville, TN; Luo, Huimin [Knoxville, TN

2008-09-09T23:59:59.000Z

3

Ionic Liquid Pretreatment Technologies  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious Rank EERE:Year in3.pdfEnergy Health andofIan KalinResearch,IntroducingIonic Liquid Pretreatment EERE

4

Hydrophobic ionic liquids  

DOE Patents [OSTI]

Ionic liquids having improved properties for application in non-aqueous batteries, electrochemical capacitors, electroplating, catalysis and chemical separations are disclosed. Exemplary compounds have one of the following formulas: ##STR1## wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, and R.sub.6 are either H; F; separate alkyl groups of from 1 to 4 carbon atoms, respectively, or joined together to constitute a unitary alkylene radical of from 2 to 4 carbon atoms forming a ring structure converging on N; or separate phenyl groups; and wherein the alkyl groups, alkylene radicals or phenyl groups may be substituted with electron withdrawing groups, preferably F--, Cl--, CF.sub.3 --, SF.sub.5 --, CF.sub.3 S--, (CF.sub.3).sub.2 CHS-- or (CF.sub.3).sub.3 CS--; and X.sup.- is a non-Lewis acid-containing polyatomic anion having a van der Waals volume exceeding 100 .ANG..sup.3.

Koch, Victor R. (Lincoln, MA); Nanjundiah, Chenniah (Lynn, MA); Carlin, Richard T. (Nashua, NH)

1998-01-01T23:59:59.000Z

5

Hydrophobic ionic liquids  

DOE Patents [OSTI]

Ionic liquids having improved properties for application in non-aqueous batteries, electrochemical capacitors, electroplating, catalysis and chemical separations are disclosed. Exemplary compounds have one of the following formulas shown in a diagram wherein R{sub 1}, R{sub 2}, R{sub 3}, R{sub 4}, R{sub 5}, and R{sub 6} are either H; F; separate alkyl groups of from 1 to 4 carbon atoms, respectively, or joined together to constitute a unitary alkylene radical of from 2 to 4 carbon atoms forming a ring structure converging on N; or separate phenyl groups; and wherein the alkyl groups, alkylene radicals or phenyl groups may be substituted with electron withdrawing groups, preferably F-, Cl-, CF{sub 3}-, SF{sub 5}-, CF{sub 3}S-, (CF{sub 3}){sub 2}CHS- or (CF{sub 3}){sub 3}CS-; and X{sup {minus}} is a non-Lewis acid-containing polyatomic anion having a van der Waals volume exceeding 100 {angstrom}{sup 3}. 4 figs.

Koch, V.R.; Nanjundiah, C.; Carlin, R.T.

1998-10-27T23:59:59.000Z

6

Ionic Liquids for Utilization of Geothermal Energy  

Broader source: Energy.gov [DOE]

DOE Geothermal Program Peer Review 2010 - Presentation. Project objective: to develop ionic liquids for two geothermal energy related applications.

7

Nanoparticle enhanced ionic liquid heat transfer fluids  

DOE Patents [OSTI]

A heat transfer fluid created from nanoparticles that are dispersed into an ionic liquid is provided. Small volumes of nanoparticles are created from e.g., metals or metal oxides and/or alloys of such materials are dispersed into ionic liquids to create a heat transfer fluid. The nanoparticles can be dispersed directly into the ionic liquid during nanoparticle formation or the nanoparticles can be formed and then, in a subsequent step, dispersed into the ionic liquid using e.g., agitation.

Fox, Elise B.; Visser, Ann E.; Bridges, Nicholas J.; Gray, Joshua R.; Garcia-Diaz, Brenda L.

2014-08-12T23:59:59.000Z

8

Early Events in Ionic Liquid Radiation Chemistry  

SciTech Connect (OSTI)

Ionic liquids are interesting and useful materials whose solvation time scales are up to thousands of times longer than in conventional solvents. The extended lifetimes of pre-solvated electrons and other energetic species in ionic liquids has profound consequences for the radiolytic product distributions and reactivity patterns. We use a newly developed, multiplexed variation of pulse-probe spectroscopy to measure the kinetics of the early dynamical and reactive events in ionic liquids.

Wishart, J.F.; Cook, A.; Rimmer, R.D.; Gohdo, M.

2010-09-14T23:59:59.000Z

9

Carbon films produced from ionic liquid carbon precursors  

DOE Patents [OSTI]

The invention is directed to a method for producing a film of porous carbon, the method comprising carbonizing a film of an ionic liquid, wherein the ionic liquid has the general formula (X.sup.+a).sub.x(Y.sup.-b).sub.y, wherein the variables a and b are, independently, non-zero integers, and the subscript variables x and y are, independently, non-zero integers, such that ax=by, and at least one of X.sup.+ and Y.sup.- possesses at least one carbon-nitrogen unsaturated bond. The invention is also directed to a composition comprising a porous carbon film possessing a nitrogen content of at least 10 atom %.

Dai, Sheng; Luo, Huimin; Lee, Je Seung

2013-11-05T23:59:59.000Z

10

Ionic Liquid Pretreatment Process for Biomass Is Successfully...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Ionic Liquid Pretreatment Process for Biomass Is Successfully Implemented at Larger Scale Ionic Liquid Pretreatment Process for Biomass Is Successfully Implemented at Larger Scale...

11

New lithium-based ionic liquid electrolytes that resist salt...  

Energy Savers [EERE]

lithium-based ionic liquid electrolytes that resist salt concentration polarization New lithium-based ionic liquid electrolytes that resist salt concentration polarization...

12

Elucidating graphene - Ionic Liquid interfacial region: a combined...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

graphene - Ionic Liquid interfacial region: a combined experimental and computational study. Elucidating graphene - Ionic Liquid interfacial region: a combined experimental and...

13

Phosphonium-based ionic liquids and uses  

DOE Patents [OSTI]

Phosphonium-based room temperature ionic liquids ("RTILs") were prepared. They were used as matrices for Matrix-Assisted Laser Desorption Ionization (MALDI) mass spectrometry and also for preparing samples of dyes for analysis.

Del Sesto, Rico E; Koppisch, Andrew T; Lovejoy, Katherine S; Purdy, Geraldine M

2014-12-30T23:59:59.000Z

14

Superbase-derived protic ionic liquids  

DOE Patents [OSTI]

Protic ionic liquids having a composition of formula (A.sup.-)(BH.sup.+) wherein A.sup.- is a conjugate base of an acid HA, and BH.sup.+ is a conjugate acid of a superbase B. In particular embodiments, BH.sup.+ is selected from phosphazenium species and guanidinium species encompassed, respectively, by the general formulas: ##STR00001## The invention is also directed to films and membranes containing these protic ionic liquids, with particular application as proton exchange membranes for fuel cells.

Dai, Sheng; Luo, Huimin; Baker, Gary A.

2013-09-03T23:59:59.000Z

15

TETRAALKYLPHOSPHONIUM POLYOXOMETALATES AS NOVEL IONIC LIQUIDS.  

SciTech Connect (OSTI)

The pairing of a Lindqvist or Keggin polyoxometalate (POM) anion with an appropriate tetraalkylphosphonium cation, [R{sub 3}R{prime}P]{sup +}, has been shown to yield an original family of ionic liquids (POM-ILs), among them salts liquid at or near ambient temperature. The physicochemical properties of several such 'inorganic liquids', in particular their thermal properties, suggests the possible application of these compounds as robust, thermally-stable solvents for liquid-liquid extraction. A preliminary evaluation of the potential of POM-ILs in this application is presented.

DIETZ,M.L.; RICKERT, P.G.; ANTONIO, M.R.; FIRESTONE, M.A.; WISHART, J.F.; SZREDER, T.

2007-11-30T23:59:59.000Z

16

Acetonitrile Drastically Boosts Conductivity of Ionic Liquids  

E-Print Network [OSTI]

We apply a new methodology in the force field generation (PCCP 2011, 13, 7910) to study the binary mixtures of five imidazolium-based room-temperature ionic liquids (RTILs) with acetonitrile (ACN). The investigated RTILs are composed of tetrafluoroborate (BF4) anion and dialkylimidazolium cations, where one of the alkyl groups is methyl for all RTILs, and the other group is different for each RTILs, being ethyl (EMIM), butyl (BMIM), hexyl (HMIM), octyl (OMIM), and decyl (DMIM). Specific densities, radial distribution functions, ionic cluster distributions, heats of vaporization, diffusion constants, shear viscosities, ionic conductivities, and their correlations are discussed. Upon addition of ACN, the ionic conductivity of RTILs is found to increase by more than 50 times, that significantly exceeds an impact of most known solvents. Remarkably, the sharpest conductivity growth is found for the long-tailed imidazolium-based cations. This new fact motivates to revisit an application of these binary systems as a...

Chaban, Vitaly V; Kalugin, Oleg N; Prezhdo, Oleg V

2012-01-01T23:59:59.000Z

17

Metal-air low temperature ionic liquid cell  

DOE Patents [OSTI]

The present application relates to an electrochemical metal-air cell in which a low temperature ionic liquid is used.

Friesen, Cody A; Buttry, Daniel A

2014-11-25T23:59:59.000Z

18

1,2,3-triazolium ionic liquids  

DOE Patents [OSTI]

The present invention relates to compositions of matter that are ionic liquids, the compositions comprising substituted 1,2,3-triazolium cations combined with any anion. Compositions of the invention should be useful in the separation of gases and, perhaps, as catalysts for many reactions.

Luebke, David; Nulwala, Hunaid; Tang, Chau

2014-12-09T23:59:59.000Z

19

Ionic Liquid-Enhanced Solid State Electrolyte Interface (SEI...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Liquid-Enhanced Solid State Electrolyte Interface (SEI) for Lithium Sulfur Batteries. Ionic Liquid-Enhanced Solid State Electrolyte Interface (SEI) for Lithium Sulfur Batteries....

20

Use of ionic liquids as coordination ligands for organometallic catalysts  

DOE Patents [OSTI]

Aspects of the present invention relate to compositions and methods for the use of ionic liquids with dissolved metal compounds as catalysts for a variety of chemical reactions. Ionic liquids are salts that generally are liquids at room temperature, and are capable of dissolving a many types of compounds that are relatively insoluble in aqueous or organic solvent systems. Specifically, ionic liquids may dissolve metal compounds to produce homogeneous and heterogeneous organometallic catalysts. One industrially-important chemical reaction that may be catalyzed by metal-containing ionic liquid catalysts is the conversion of methane to methanol.

Li, Zaiwei (Moreno Valley, CA); Tang, Yongchun (Walnut, CA); Cheng; Jihong (Arcadia, CA)

2009-11-10T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

Compositions and methods useful for ionic liquid treatment of biomass  

SciTech Connect (OSTI)

The present invention provides for novel compositions and methods for recycling or recovering ionic liquid used in IL pretreated cellulose and/or lignocellulosic biomass (LBM).

Dibble, Dean C.; Cheng, Aurelia; George, Anthe

2014-07-29T23:59:59.000Z

22

Ionic Liquids as Novel Engine Lubricants or Lubricant Additives...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Additives Ionic Liquids as Novel Engine Lubricants or Lubricant Additives Bench test results showed that compared with fully-formulated engine oils, selected low-viscosity...

23

Lipid extraction from microalgae using a single ionic liquid  

DOE Patents [OSTI]

A one-step process for the lysis of microalgae cell walls and separation of the cellular lipids for use in biofuel production by utilizing a hydrophilic ionic liquid, 1-butyl-3-methylimidazolium. The hydrophilic ionic liquid both lyses the microalgae cell walls and forms two immiscible layers, one of which consists of the lipid contents of the lysed cells. After mixture of the hydrophilic ionic liquid with a suspension of microalgae cells, gravity causes a hydrophobic lipid phase to move to a top phase where it is removed from the mixture and purified. The hydrophilic ionic liquid is recycled to lyse new microalgae suspensions.

Salvo, Roberto Di; Reich, Alton; Dykes, Jr., H. Waite H.; Teixeira, Rodrigo

2013-05-28T23:59:59.000Z

24

Aprotic Heterocyclic Anion Triazolide Ionic Liquids - A New Class of Ionic Liquid Anion Accessed by the Huisgen Cycloaddition Reaction  

SciTech Connect (OSTI)

The triazole core is a highly versatile heterocyclic ring which can be accessed easily with the Cu(I)-catalyzed Huisgen cycloaddition reaction. Herein we present the preparation of ionic liquids that incorporate a 1,2,3-triazolide anion. These ionic liquids were prepared by a facile procedure utilizing a base-labile pivaloylmethyl group at the 1-position, which can act as precursors to 1H- 4-substituted 1,2,3-triazole. These triazoles were then subsequently converted into ionic liquids after deprotonation using an appropriate ionic liquid cation hydroxide. The densities and thermal decompositions of these ionic liquids were measured. These novel ionic liquids have potential applications in gas separations and in metal-free catalysis.

Thompson, Robert L.; Damodaran, Krishnan; Luebke, David; Nulwala, Hunaid

2013-06-01T23:59:59.000Z

25

Durable electrooptic devices comprising ionic liquids  

DOE Patents [OSTI]

Electrolyte solutions for electrochromic devices such as rear view mirrors and displays with low leakage currents are prepared using inexpensive, low conductivity conductors. Preferred electrolytes include bifunctional redox dyes and molten salt solvents with enhanced stability toward ultraviolet radiation. The solvents include lithium or quaternary ammonium cations, and perfluorinated sulfonylimide anions selected from trifluoromethylsulfonate (CF3SO3-), bis(trifluoromethylsulfonyl)imide ((CF3SO2)2N-), bis(perfluoroethylsulfonyl)imide ((CF3CF2SO2)2N-) and tris(trifluoromethylsulfonyl)methide ((CF3SO2)3C-). Electroluminescent, electrochromic and photoelectrochromic devices with nanostructured electrodes include ionic liquids with bifunctional redox dyes.

Agrawal, Anoop (Tucson, AZ); Cronin, John P. (Tucson, AZ); Tonazzi, Juan C. L. (Tucson, AZ); Warner, Benjamin P. (Los Alamos, NM); McCleskey, T. Mark (Los Alamos, NM); Burrell, Anthony K. (Los Alamos, NM)

2005-11-01T23:59:59.000Z

26

Ionic liquid assisted hydrothermal fabrication of hierarchically organized ?-AlOOH hollow sphere  

SciTech Connect (OSTI)

Highlights: ? The ?-AlOOH hollow spheres were synthesized via an ionic liquid-assisted hydrothermal treatment. ? Ionic liquid plays an important role in the morphology of the product. ? Ionic liquid can be easily removed from the product and reused in next experiment. ? A “aggregation–solution–recrystallization” formation mechanism may occur in the system. -- Abstract: Hierarchically organized ?-AlOOH hollow spheres with nanoflake-like porous surface texture have been successfully synthesized via an ionic liquid-assisted hydrothermal synthesis method in citric acid monohydrate (CAMs). It was found that ionic liquid [bmim]{sup +}Cl{sup ?} played an important role in the morphology of the product due to its strong interactions with reaction particles. The samples were characterized by X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), Scanning Electron Microscope (SEM) and Transmission Electron Microscopy (TEM). The results show that the product has narrow particle size distribution (500–900 nm particle diameter range), high specific surface area (240.5 m{sup 2}/g) and large pore volume (0.61 cm{sup 3}/g). The corresponding ?-Al{sub 2}O{sub 3} hollow spheres can be obtained by calcining it at 550 °C for 3 h. The proposed formation mechanism and other influencing factors of the ?-AlOOH hollow sphere material, such as reaction temperature, reaction duration, CAMs and urea, have also been investigated.

Tang, Zhe, E-mail: tangzhe1983@163.com [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China)] [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China); Liu, Yunqi, E-mail: liuyq@upc.edu.cn [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China)] [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China); Li, Guangci, E-mail: liguangci1984@yahoo.com.cn [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China)] [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China); Hu, Xiaofu, E-mail: hjj19850922@126.cn [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China)] [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China); Liu, Chenguang, E-mail: cgliu@upc.edu.cn [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China)] [State Key Laboratory of Heavy Oil Processing, Key Laboratory of Catalysis, China National Petroleum Corporation (CNPC), China University of Petroleum (East China), Qingdao 266555 (China)

2012-11-15T23:59:59.000Z

27

Durable Electrooptic Devices Comprising Ionic Liquids  

DOE Patents [OSTI]

Electrolyte solutions for electrochromic devices such as rear view mirrors and displays with low leakage currents are prepared using inexpensive, low conductivity conductors. Preferred electrolytes include bifunctional redox dyes and molten salt solvents with enhanced stability toward ultraviolet radiation. The solvents include lithium or quaternary ammonium cations, and perfluorinated sulfonylimide anions selected from trifluoromethylsulfonate (CF.sub.3SO.sub.3.sup.-), bis(trifluoromethylsulfonyl)imide ((CF.sub.3SO.sub.2).sub.2N.sup.-), bis(perfluoroethylsulfonyl)imide ((CF.sub.3CF.sub.2SO.sub.2).sub.2N.sup.-) and tris(trifluoromethylsulfonyl)methide ((CF.sub.3SO.sub.2).sub.3C.sup.-). Electroluminescent, electrochromic and photoelectrochromic devices with nanostructured electrodes include ionic liquids with bifunctional redox dyes. Some of the electrolyte solutions color to red when devices employing the solutions are powered, leading to red or neutral electrooptic devices.

Burrell, Anthony K. (Los Alamos, NM); Agrawal, Anoop (Tucson, AZ); Cronin, John P. (Tucson, AZ); Tonazzi, Juan C. L. (Tucson, AZ); Warner, Benjamin P. (Los Alamos, NM); McCleskey, T. Mark (Los Alamos, NM)

2008-11-11T23:59:59.000Z

28

Durable electrooptic devices comprising ionic liquids  

DOE Patents [OSTI]

Electrolyte solutions for electrochromic devices such as rear view mirrors and displays with low leakage currents are prepared using inexpensive, low conductivity conductors. Preferred electrolytes include bifunctional redox dyes and molten salt solvents with enhanced stability toward ultraviolet radiation. The solvents include lithium or quaternary ammonium cations, and perfluorinated sulfonylimide anions selected from trifluoromethylsulfonate (CF.sub.3SO.sub.3.sup.-), bis(trifluoromethylsulfonyl)imide ((CF.sub.3SO.sub.2).sub.2N.sup.-), bis(perfluoroethylsulfonyl)imide ((CF.sub.3CF.sub.2SO.sub.2).sub.2N.sup.-) and tris(trifluoromethylsulfonyl)methide ((CF.sub.3SO.sub.2).sub.3C.sup.-). Electroluminescent, electrochromic and photoelectrochromic devices with nanostructured electrodes include ionic liquids with bifunctional redox dyes.

Warner, Benjamin P. (Los Alamos, NM); McCleskey, T. Mark (Los Alamos, NM); Burrell, Anthony K. (Los Alamos, NM)

2006-10-10T23:59:59.000Z

29

Durable electrooptic devices comprising ionic liquids  

DOE Patents [OSTI]

Electrolyte solutions for electrochromic devices such as rear view mirrors and displays with low leakage currents are prepared using inexpensive, low conductivity conductors. Preferred electrolytes include bifunctional redox dyes and molten salt solvents with enhanced stability toward ultraviolet radiation. The solvents include lithium or quaternary ammonium cations, and perfluorinated sulfonylimide anions selected from trifluoromethylsulfonate (CF.sub.3SO.sub.3.sup.-), bis(trifluoromethylsulfonyl)imide ((CF.sub.3SO.sub.2).sub.2N.sup.-), bis(perfluoroethylsulfonyl)imide ((CF.sub.3CF.sub.2SO.sub.2).sub.2N.sup.-) and tris(trifluoromethylsulfonyl)methide ((CF.sub.3SO.sub.2).sub.3C.sup.-). Electroluminescent, electrochromic and photoelectrochromic devices with nanostructured electrodes include ionic liquids with bifunctional redox dyes. Some of the electrolyte solutions color to red when devices employing the solutions are powered, leading to red or neutral electrooptic devices.

Burrell, Anthony K. (Los Alamos, NM); Agrawal, Anoop (Tucson, AZ); Cronin; John P. (Tucson, AZ); Tonazzi, Juan C. L. (Tucson, AZ); Warner, Benjamin P. (Los Alamos, NM); McCleskey, T. Mark (Los Alamos, NM)

2009-12-15T23:59:59.000Z

30

Gelled Ionic Liquid-Based Membranes: Achieving a 10,000 GPU Permeance for Post-Combustion Carbon Capture with Gelled Ionic Liquid-Based Membranes  

SciTech Connect (OSTI)

IMPACCT Project: Alongside Los Alamos National Laboratory and the Electric Power Research Institute, CU-Boulder is developing a membrane made of a gelled ionic liquid to capture CO2 from the exhaust of coal-fired power plants. The membranes are created by spraying the gelled ionic liquids in thin layers onto porous support structures using a specialized coating technique. The new membrane is highly efficient at pulling CO2 out of coal-derived flue gas exhaust while restricting the flow of other materials through it. The design involves few chemicals or moving parts and is more mechanically stable than current technologies. The team is now working to further optimize the gelled materials for CO2 separation and create a membrane layer that is less than 1 micrometer thick.

None

2011-02-02T23:59:59.000Z

31

Modeling Liquid-Liquid Equilibrium of Ionic Liquid Systems with NRTL, Electrolyte-NRTL, and UNIQUAC  

E-Print Network [OSTI]

Modeling Liquid-Liquid Equilibrium of Ionic Liquid Systems with NRTL, Electrolyte-NRTL, and UNIQUAC different excess Gibbs free energy models are evaluated: the NRTL, UNIQUAC and electrolyte- NRTL (eNRTL) models. In the case of eNRTL, a new formulation of the model is used, based on a symmetric reference

Stadtherr, Mark A.

32

Soft ionization of thermally evaporated hypergolic ionic liquid aerosols  

SciTech Connect (OSTI)

Isolated ion pairs of a conventional ionic liquid, 1-Ethyl-3-Methyl-Imidazolium Bis(trifluoromethylsulfonyl)imide ([Emim+][Tf2N?]), and a reactive hypergolic ionic liquid, 1- Butyl-3-Methyl-Imidazolium Dicyanamide ([Bmim+][Dca?]), are generated by vaporizing ionic liquid submicron aerosol particles for the first time; the vaporized species are investigated by dissociative ionization with tunable vacuum ultraviolet (VUV) light, exhibiting clear intact cations, Emim+ and Bmim+, presumably originating from intact ion pairs. Mass spectra of ion pair vapor from an effusive source of the hypergolic ionic liquid show substantial reactive decomposition due to the internal energy of the molecules emanating from the source. Photoionization efficiency curves in the near threshold ionization region of isolated ion pairs of [Emim+][Tf2N?] ionic liquid vapor are compared for an aerosol source and an effusive source, revealing changes in the appearance energy due to the amount of internal energy in the ion pairs. The aerosol source has a shift to higher threshold energy (~;;0.3 eV), attributed to reduced internal energy of the isolated ion pairs. The method of ionic liquid submicron aerosol particle vaporization, for reactive ionic liquids such as hypergolic species, is a convenient, thermally ?cooler? source of isolated intact ion pairs in the gas phase compared to effusive sources.

University of California; ERC, Incorporated, Edwards Air Force Base; Air Force Research Laboratory, Edwards Air Force Base; National Synchrotron Radiation Research Center (NSRRC); Koh, Christine J.; Liu, Chen-Lin; Harmon, Christopher W.; Strasser, Daniel; Golan, Amir; Kostko, Oleg; Chambreau, Steven D.; L.Vaghjiani, Ghanshyam; Leone, Stephen R.

2012-03-16T23:59:59.000Z

33

Kinetics and Solvent Effects in the Synthesis of Ionic Liquids  

E-Print Network [OSTI]

in diesel fuel 19 and extractants in the recovery of ethanol and butanol for biofuel applications. 20 1.1. IL Background ILs have shown versatility in many fields of research and applications, so the question is what are ILs, and what makes ILs so... with ionic liquids. Chem. Commun. 2001, 2494-2495. 20. Fadeev, A. G.; Meagher, M. M., Opportunities for ionic liquids in recovery of biofuels. Chem. Commun. 2001, 295-296. 21. Lancaster, L., Organic reactivity in ionic liquids: some mechanistic insights...

Schleicher, Jay C.

2007-12-12T23:59:59.000Z

34

Phase-Changing Ionic Liquids: CO2 Capture with Ionic Liquids Involving Phase Change  

SciTech Connect (OSTI)

IMPACCT Project: Notre Dame is developing a new CO2 capture process that uses special ionic liquids (ILs) to remove CO2 from the gas exhaust of coal-fired power plants. ILs are salts that are normally liquid at room temperature, but Notre Dame has discovered a new class of ILs that are solid at room temperature and change to liquid when they bind to CO2. Upon heating, the CO2 is released for storage, and the ILs re-solidify and donate some of the heat generated in the process to facilitate further CO2 release. These new ILs can reduce the energy required to capture CO2 from the exhaust stream of a coal-fired power plant when compared to state-ofthe- art technology.

None

2010-07-01T23:59:59.000Z

35

Tribological Properties of Ionic Liquids Lubricants Containing Nanoparticles  

E-Print Network [OSTI]

Recently, there has been an increase in research in the application of ionic liquids containing nanoparticles as lubricants due to their properties such as thermally stability, non-volatility and non-flammability. The purpose of this thesis...

Lu, Wei

2014-05-14T23:59:59.000Z

36

Molecular Dynamics Modeling of Ionic Liquids in Electrospray Propulsion  

E-Print Network [OSTI]

. Lozano June 2010 SSL # 6-10 #12;#12;Molecular Dynamics Modeling of Ionic Liquids in Electrospray Propulsion Nanako Takahashi, Paulo C. Lozano June 2010 SSL # 6-10 This work is based on the unaltered text

37

Shear and Extensional Rheology of Cellulose/Ionic Liquid Solutions  

E-Print Network [OSTI]

In this study, we characterize the shear and extensional rheology of dilute to semidilute solutions of cellulose in the ionic liquid 1-ethyl-3-methylimidazolium acetate (EMIAc). In steady shear flow, the semidilute solutions ...

Haward, Simon J.

38

The radiation chemistry of ionic liquids: a review  

SciTech Connect (OSTI)

Ionic liquids have received increasing attention as media for radiochemical separations. Recent literature includes examinations of the efficiencies and mechanisms of the solvent extraction of lanthanides, actinides and fission products into ionic liquid solutions. For radiochemical applications, including as replacement solvents for nuclear fuel reprocessing, a thorough understanding of the radiation chemistry of ionic liquids will be required. Such an understanding can be achieved based upon a combination of steady-state radiolysis experiments coupled with post-irradiation product identification and pulse-radiolysis experiments to acquire kinetic information. These techniques allow for the elucidation of radiolytic mechanisms. This contribution reviews the current ionic liquid radiation chemistry literature as it affects separations, with these considerations in mind.

Bruce J. Mincher; James F. Wishart

2014-07-01T23:59:59.000Z

39

Membrane contactor assisted extraction/reaction process employing ionic liquids  

DOE Patents [OSTI]

The present invention relates to a functionalized membrane contactor extraction/reaction system and method for extracting target species from multi-phase solutions utilizing ionic liquids. One preferred embodiment of the invented method and system relates to an extraction/reaction system wherein the ionic liquid extraction solutions act as both extraction solutions and reaction mediums, and allow simultaneous separation/reactions not possible with prior art technology.

Lin, Yupo J. (Naperville, IL); Snyder, Seth W. (Lincolnwood, IL)

2012-02-07T23:59:59.000Z

40

Method and apparatus using an active ionic liquid for algae biofuel harvest and extraction  

DOE Patents [OSTI]

The invention relates to use of an active ionic liquid to dissolve algae cell walls. The ionic liquid is used to, in an energy efficient manner, dissolve and/or lyse an algae cell walls, which releases algae constituents used in the creation of energy, fuel, and/or cosmetic components. The ionic liquids include ionic salts having multiple charge centers, low, very low, and ultra low melting point ionic liquids, and combinations of ionic liquids. An algae treatment system is described, which processes wet algae in a lysing reactor, separates out algae constituent products, and optionally recovers the ionic liquid in an energy efficient manner.

Salvo, Roberto Di; Reich, Alton; Dykes, Jr., H. Waite H.; Teixeira, Rodrigo

2012-11-06T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Electronically and ionically conductive porous material and method for manufacture of resin wafers therefrom  

DOE Patents [OSTI]

An electrically and ionically conductive porous material including a thermoplastic binder and one or more of anion exchange moieties or cation exchange moieties or mixtures thereof and/or one or more of a protein capture resin and an electrically conductive material. The thermoplastic binder immobilizes the moieties with respect to each other but does not substantially coat the moieties and forms the electrically conductive porous material. A wafer of the material and a method of making the material and wafer are disclosed.

Lin, YuPo J. (Naperville, IL); Henry, Michael P. (Batavia, IL); Snyder, Seth W. (Lincolnwood, IL)

2008-11-18T23:59:59.000Z

42

Electronically and ionically conductive porous material and method for manufacture of resin wafers therefrom  

DOE Patents [OSTI]

An electrically and ionically conductive porous material including a thermoplastic binder and one or more of anion exchange moieties or cation exchange moieties or mixtures thereof and/or one or more of a protein capture resin and an electrically conductive material. The thermoplastic binder immobilizes the moieties with respect to each other but does not substantially coat the moieties and forms the electrically conductive porous material. A wafer of the material and a method of making the material and wafer are disclosed.

Lin, YuPo J. (Naperville, IL); Henry, Michael P. (Batavia, IL); Snyder, Seth W. (Lincolnwood, IL)

2011-07-12T23:59:59.000Z

43

Physically and chemically stable ionic liquid-infused textured surfaces showing excellent dynamic omniphobicity  

SciTech Connect (OSTI)

A fluorinated and hydrophobic ionic liquid (IL), 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide, effectively served as an advantageous lubricating liquid for the preparation of physically and chemically stable omniphobic surfaces based on slippery liquid-infused porous surfaces. Here, we used particulate microstructures as supports, prepared by the chemical vapor deposition of 1,3,5,7-tetramethylcyclotetrasiloxane and subsequent surface modification with (3-aminopropyl)triethoxysilane. Confirmed by SEM and contact angle measurements, the resulting IL-infused microtextured surfaces are smooth and not only water but also various low surface tension liquids can easily slide off at low substrate tilt angles of <5°, even after exposure to high temperature, vacuum, and UV irradiation.

Miranda, Daniel F.; Urata, Chihiro; Masheder, Benjamin; Dunderdale, Gary J.; Hozumi, Atsushi, E-mail: a.hozumi@aist.go.jp [National Institute of Advanced Industrial Science and Technology (AIST), 2266-98, Anagahora, Shimo-Shidami, Moriyama-ku, Nagoya, Aichi 463-8560 (Japan); Yagihashi, Makoto [Nagoya Municipal Industrial Research Institute, Rokuban, Atsuta-ku, Nagoya 456-0058 (Japan)

2014-05-01T23:59:59.000Z

44

Methods for separating medical isotopes using ionic liquids  

SciTech Connect (OSTI)

A method for extracting a radioisotope from an aqueous solution, the method comprising: a) intimately mixing a non-chelating ionic liquid with the aqueous solution to transfer at least a portion of said radioisotope to said non-chelating ionic liquid; and b) separating the non-chelating ionic liquid from the aqueous solution. In preferred embodiments, the method achieves an extraction efficiency of at least 80%, or a separation factor of at least 1.times.10.sup.4 when more than one radioisotope is included in the aqueous solution. In particular embodiments, the method is applied to the separation of medical isotopes pairs, such as Th from Ac (Th-229/Ac-225, Ac-227/Th-227), or Ra from Ac (Ac-225 and Ra-225, Ac-227 and Ra-223), or Ra from Th (Th-227 and Ra-223, Th-229 and Ra-225).

Luo, Huimin; Boll, Rose Ann; Bell, Jason Richard; Dai, Sheng

2014-10-21T23:59:59.000Z

45

Energy Efficient Electrochromic Windows Incorporating Ionic Liquids  

SciTech Connect (OSTI)

One approach to increasing the energy efficiency of windows is to control the amount of solar radiation transmitted through a window by using electrochromic technology. What is unique about this project is that the electrochromic is based on the reduction/oxidation reactions of cathodic and anodic organic semi-conducting polymers using room temperature ionic liquids as ion transport electrolytes. It is believed that these types of coatings would be a lower cost alternative to traditional all inorganic thin film based electrochromic technologies. Although there are patents1 based on the proposed technology, it has never been reduced to practice and thoroughly evaluated (i.e. durability and performance) in a window application. We demonstrate that by using organic semi-conductive polymers, specific bands of the solar spectrum (specifically visible and near infrared) can be targeted for electrochemical variable transmittance responsiveness. In addition, when the technology is incorporated into an insulating glass unit, the energy parameters such as the solar heat gain coefficient and the light to solar gain ratio are improved over that of a typical insulating glass unit comprised of glass with a low emissivity coating. A minimum of {approx}0.02 quads of energy savings per year with a reduction of carbon emissions for electricity of {approx}320 MKg/yr benefit is achieved over that of a typical insulating glass unit including a double silver low-E coating. Note that these values include a penalty in the heating season. If this penalty is removed (i.e. in southern climates or commercial structures where cooling is predominate year-round) a maximum energy savings of {approx}0.05 quad per year and {approx}801 MKg/yr can be achieved over that of a typical insulating glass unit including a double silver low-E coating. In its current state, the technology is not durable enough for an exterior window application. The primary downfall is that the redox chemistry fails to recover to a bleached state upon exposure to heat and solar radiation while being cycled over time from the bleached to the dark state. Most likely the polymers are undergoing degradation reactions which are accelerated by heat and solar exposure while in either the reduced or oxidized states and the performance of the polymers is greatly reduced over time. For this technology to succeed in an exterior window application, there needs to be more work done to understand the degradation of the polymers under real-life application conditions such as elevated temperatures and solar exposure so that recommendations for improvements in to the overall system can be made. This will be the key to utilizing this type of technology in any future real-life applications.

Cheri Boykin; James Finley; Donald Anthony; Julianna Knowles; Richard Markovic; Michael Buchanan; Mary Ann Fuhry; Lisa Perrine

2008-11-30T23:59:59.000Z

46

Low Temperature Reduction of Alumina Using Fluorine Containing Ionic Liquids  

SciTech Connect (OSTI)

The major objective of the project is to establish the feasibility of using specific ionic liquids capable of sustaining aluminum electrolysis near room temperature at laboratory and batch recirculation scales. It will explore new technologies for aluminum and other valuable metal extraction and process methods. The new technology will overcome many of the limitations associated with high temperatures processes such as high energy consumption and corrosion attack. Furthermore, ionic liquids are non-toxic and could be recycled after purification, thus minimizing extraction reagent losses and environmental pollutant emissions. Ionic liquids are mixture of inorganic and organic salts which are liquid at room temperature and have wide operational temperature range. During the last several years, they were emerging as novel electrolytes for extracting and refining of aluminum metals and/or alloys, which are otherwise impossible using aqueous media. The superior high temperature characteristics and high solvating capabilities of ionic liquids provide a unique solution to high temperature organic solvent problems associated with device internal pressure build-up, corrosion, and thermal stability. However their applications have not yet been fully implemented due to the insufficient understanding of the electrochemical mechanisms involved in processing of aluminum with ionic liquids. Laboratory aluminum electrodeposition in ionic liquids has been investigated in chloride and bis (trifluoromethylsulfonyl) imide based ionic liquids. The electrowinning process yielded current density in the range of 200-500 A/m2, and current efficiency of about 90%. The results indicated that high purity aluminum (>99.99%) can be obtained as cathodic deposits. Cyclic voltammetry and chronoamperometry studies have shown that initial stages of aluminum electrodeposition in ionic liquid electrolyte at 30°C was found to be quasi-reversible, with the charge transfer coefficient (0.40). Nucleation phenomena involved in aluminum deposition on copper in AlCl3-BMIMCl electrolyte was found to be instantaneous followed by diffusion controlled three-dimensional growth of nuclei. Diffusion coefficient (Do) of the electroactive species Al2Cl7¯ ion was in the range from 6.5 to 3.9×10–7 cm2?s–1 at a temperature of 30°C. Relatively little research efforts have been made toward the fundamental understanding and modeling of the species transport and transformation information involved in ionic liquid mixtures, which eventually could lead to quantification of electrochemical properties. Except that experimental work in this aspect usually is time consuming and expensive, certain characteristics of ionic liquids also made barriers for such analyses. Low vapor pressure and high viscosity make them not suitable for atomic absorption spectroscopic measurement. In addition, aluminum electrodeposition in ionic liquid electrolytes are considered to be governed by multi-component mass, heat and charge transport in laminar and turbulent flows that are often multi-phase due to the gas evolution at the electrodes. The kinetics of the electrochemical reactions is in general complex. Furthermore, the mass transfer boundary layer is about one order of magnitude smaller than the thermal and hydrodynamic boundary layer (Re=10,000). Other phenomena that frequently occur are side reactions and temperature or concentration driven natural convection. As a result of this complexity, quantitative knowledge of the local parameters (current densities, ion concentrations, electrical potential, temperature, etc.) is very difficult to obtain. This situation is a serious obstacle for improving the quality of products, efficiency of manufacturing and energy consumption. The gap between laboratory/batch scale processing with global process control and nanoscale deposit surface and materials specifications needs to be bridged. A breakthrough can only be realized if on each scale the occurring phenomena are understood and quantified. Multiscale numerical modeling nevertheless can help t

Dr. R. G. Reddy

2007-09-01T23:59:59.000Z

47

Sum frequency generation study on the orientation of room-temperature ionic liquid at the grapheneionic liquid interface  

E-Print Network [OSTI]

such as dye-sensitized solar cells and super capacitors, room-temperature ionic liquids are considered

Bao, Jiming

48

Charge Transport and Glassy Dynamics in Ionic Liquids  

SciTech Connect (OSTI)

Ionic liquids (ILs) exhibit unique features such as low melting points, low vapor pressures, wide liquidus temperature ranges, high thermal stability, high ionic conductivity, and wide electrochemical windows. As a result, they show promise for use in variety of applications: as reaction media, in batteries and supercapacitors, in solar and fuel cells, for electrochemical deposition of metals and semiconductors, for protein extraction and crystallization, and many others. Because of the ease with which they can be supercooled, ionic liquids offer new opportunities to investigate long-standing questions regarding the nature of the dynamic glass transition and its possible link to charge transport. Despite the significant steps achieved from experimental and theoretical studies, no generally accepted quantitative theory of dynamic glass transition to date has been capable of reproducing all the experimentally observed features. In this Account, we discuss recent studies of the interplay between charge transport and glassy dynamics in ionic liquids as investigated by a combination of several experimental techniques including broadband dielectric spectroscopy, pulsed field gradient nuclear magnetic resonance, dynamic mechanical spectroscopy, and differential scanning calorimetry. Based on EinsteinSmoluchowski relations, we use dielectric spectra of ionic liquids to determine diffusion coefficients in quantitative agreement with independent pulsed field gradient nuclear magnetic resonance measurements, but spanning a broader range of more than 10 orders of magnitude. This approach provides a novel opportunity to determine the electrical mobility and effective number density of charge carriers as well as their types of thermal activation from the measured dc conductivity separately. We also unravel the origin of the remarkable universality of charge transport in different classes of glass-forming ionic liquids.

Sangoro, Joshua R [ORNL; Kremer, Friedrich [University of Leipzig

2012-01-01T23:59:59.000Z

49

Characterization of an iodine-based ionic liquid ion source and studies on ion fragmentation  

E-Print Network [OSTI]

Electrosprays are a well studied source of charged droplets and ions. A specific subclass is the ionic liquid ion source (ILIS), which produce ion beams from the electrostatically stressed meniscus of ionic liquids. ILIS ...

Fedkiw, Timothy Peter

2010-01-01T23:59:59.000Z

50

Growth of flower-like CdSe dendrites from a Brnsted acidbase ionic liquid precursor{  

E-Print Network [OSTI]

solution of water, ethanol and ionic liquid based on formic acid and N,N-dimethylformamide. Experimental, ethanol, an ionic liquid based on formic acid and N,N-dimethylformamide, cadmium chloride and sel

Utrecht, Universiteit

51

Fabrication of fiber supported ionic liquids and methods of use  

DOE Patents [OSTI]

One or more embodiments relates to the production of a fabricated fiber having an asymmetric polymer network and having an immobilized liquid such as an ionic liquid within the pores of the polymer network. The process produces the fabricated fiber in a dry-wet spinning process using a homogenous dope solution, providing significant advantage over current fabrication methods for liquid-supporting polymers. The fabricated fibers may be effectively utilized for the separation of a chemical species from a mixture based on the selection of the polymer, the liquid, and the solvent utilized in the dope.

Luebke, David R; Wickramanayake, Shan

2013-02-26T23:59:59.000Z

52

High performance ultracapacitors with carbon nanomaterials and ionic liquids  

DOE Patents [OSTI]

The present invention is directed to the use of carbon nanotubes and/or electrolyte structures in various electrochemical devices, such as ultracapacitors having an ionic liquid electrolyte. The carbon nanotubes are preferably aligned carbon nanotubes. Compared to randomly entangled carbon nanotubes, aligned carbon nanotubes can have better defined pore structures and higher specific surface areas.

Lu, Wen; Henry, Kent Douglas

2012-10-09T23:59:59.000Z

53

Method for synthesis of titanium dioxide nanotubes using ionic liquids  

SciTech Connect (OSTI)

The invention is directed to a method for producing titanium dioxide nanotubes, the method comprising anodizing titanium metal in contact with an electrolytic medium containing an ionic liquid. The invention is also directed to the resulting titanium dioxide nanotubes, as well as devices incorporating the nanotubes, such as photovoltaic devices, hydrogen generation devices, and hydrogen detection devices.

Qu, Jun; Luo, Huimin; Dai, Sheng

2013-11-19T23:59:59.000Z

54

High performance batteries with carbon nanomaterials and ionic liquids  

DOE Patents [OSTI]

The present invention is directed to lithium-ion batteries in general and more particularly to lithium-ion batteries based on aligned graphene ribbon anodes, V.sub.2O.sub.5 graphene ribbon composite cathodes, and ionic liquid electrolytes. The lithium-ion batteries have excellent performance metrics of cell voltages, energy densities, and power densities.

Lu, Wen (Littleton, CO)

2012-08-07T23:59:59.000Z

55

Importance of glassy fragility for energy applications of ionic liquids  

E-Print Network [OSTI]

Ionic liquids (ILs) are salts that are liquid close to room temperature. Their possible applications are numerous, e.g., as solvents for green chemistry in various electrochemical devices, and even for such "exotic" purposes as spinning-liquid mirrors for lunar telescopes. Here we concentrate on their use for new advancements in energy-storage and -conversion devices: Batteries, supercapacitors or fuel cells using ILs as electrolytes could be important building blocks for the sustainable energy supply of tomorrow. Interestingly, ILs show glassy freezing and the universal, but until now only poorly understood dynamic properties of glassy matter, dominate many of their physical properties. We show that the conductivity of ILs, an essential figure of merit for any electrochemical application, depends in a systematic way not only on their glass temperature but also on the so-called fragility, characterizing the non-canonical super-Arrhenius temperature dependence of their ionic mobility.

P. Sippel; P. Lunkenheimer; S. Krohns; E. Thoms; A. Loidl

2015-02-24T23:59:59.000Z

56

Extraordinarily Efficient Conduction in a Redox-Active Ionic Liquid  

E-Print Network [OSTI]

Iodine added to iodide-based ionic liquids leads to extraordinarily efficient charge transport, vastly exceeding that expected for such viscous systems. Using terahertz time-domain spectroscopy, in conjunction with dc conductivity, diffusivity and viscosity measurements we unravel the conductivity pathways in 1-methyl-3-propylimidazolium iodide melts. This study presents evidence of the Grotthuss mechanism as a significant contributor to the conductivity, and provides new insights into ion pairing processes as well as the formation of polyiodides. The terahertz and transport results are reunited in a model providing a quantitative description of the conduction by physical diffusion and the Grotthuss bond-exchange process. These novel results are important for the fundamental understanding of conduction in molten salts and for applications where ionic liquids are used as charge-transporting media such as in batteries and dye-sensitized solar cells.

Verner K. Thorsmølle; Guido Rothenberger; Daniel Topgaard; Jan C. Brauer; Dai-Bin Kuang; Shaik M. Zakeeruddin; Björn Lindman; Michael Grätzel; Jacques-E. Moser

2010-11-09T23:59:59.000Z

57

Ionic liquids for separation of olefin-paraffin mixtures  

DOE Patents [OSTI]

The invention is directed to an ionic liquid comprising (i) a cationic portion containing a complex of a silver (I) ion and one or more neutral ligands selected from organoamides, organoamines, olefins, and organonitriles, and (ii) an anionic portion having the chemical formula ##STR00001## wherein m and n are independently 0 or an integer of 1 or above, and p is 0 or 1, provided that when p is 0, the group --N--SO.sub.2--(CF.sub.2).sub.nCF.sub.3 subtended by p is replaced with an oxide atom connected to the shown sulfur atom. The invention is also directed to a method for separating an olefin from an olefin-paraffin mixture by passing the mixture through a layer of the ionic liquid described above.

Dai, Sheng; Luo, Huimin; Huang, Jing-Fang

2013-09-17T23:59:59.000Z

58

Ionic liquids for separation of olefin-paraffin mixtures  

DOE Patents [OSTI]

The invention is directed to an ionic liquid comprising (i) a cationic portion containing a complex of a silver (I) ion and one or more neutral ligands selected from organoamides, organoamines, olefins, and organonitriles, and (ii) an anionic portion having the chemical formula ##STR00001## wherein m and n are independently 0 or an integer of 1 or above, and p is 0 or 1, provided that when p is 0, the group --N--SO.sub.2--(CF.sub.2).sub.nCF.sub.3 subtended by p is replaced with an oxide atom connected to the shown sulfur atom. The invention is also directed to a method for separating an olefin from an olefin-paraffin mixture by passing the mixture through a layer of the ionic liquid described above.

Dai, Sheng; Luo, Huimin; Huang, Jing-Fang

2014-07-15T23:59:59.000Z

59

Reactions of Lignin Model Compounds in Ionic Liquids  

SciTech Connect (OSTI)

Lignin, a readily available form of biomass, awaits novel chemistry for converting it to valuable aromatic chemicals. Recent work has demonstrated that ionic liquids are excellent solvents for processing woody biomass and lignin. Seeking to exploit ionic liquids as media for depolymerization of lignin, we investigated reactions of lignin model compounds in these solvents. Using Brønsted acid catalysts in 1-ethyl-3-methylimidazolium triflate at moderate temperatures, we obtained up to 11.6% yield of the dealkylation product guaiacol from the model compound eugenol and cleaved phenethyl phenyl ether, a model for lignin ethers. Despite these successes, acid catalysis failed in dealkylation of the unsaturated model compound 4-ethylguaiacol and did not produce monomeric products from organosolv lignin, demonstrating that further work is required to understand the complex chemistry of lignin depolymerization.

Holladay, John E.; Binder, Joseph B.; Gray, Michel J.; White, James F.; Zhang, Z. Conrad

2009-09-15T23:59:59.000Z

60

MINOR ACTINIDE SEPARATIONS USING ION EXCHANGERS OR IONIC LIQUIDS  

SciTech Connect (OSTI)

This project seeks to determine if (1) inorganic-based ion exchange materials or (2) electrochemical methods in ionic liquids can be exploited to provide effective Am and Cm separations. Specifically, we seek to understand the fundamental structural and chemical factors responsible for the selectivity of inorganic-based ion-exchange materials for actinide and lanthanide ions. Furthermore, we seek to determine whether ionic liquids can serve as the electrolyte that would enable formation of higher oxidation states of Am and other actinides. Experiments indicated that pH, presence of complexants and Am oxidation state exhibit significant influence on the uptake of actinides and lanthanides by layered sodium titanate and hybrid zirconium and tin phosphonate ion exchangers. The affinity of the ion exchangers increased with increasing pH. Greater selectivity among Ln(III) ions with sodium titanate materials occurs at a pH close to the isoelectric potential of the ion exchanger. The addition of DTPA decreased uptake of Am and Ln, whereas the addition of TPEN generally increases uptake of Am and Ln ions by sodium titanate. Testing confirmed two different methods for producing Am(IV) by oxidation of Am(III) in ionic liquids (ILs). Experimental results suggest that the unique coordination environment of ionic liquids inhibits the direct electrochemical oxidation of Am(III). The non-coordinating environment increases the oxidation potential to a higher value, while making it difficult to remove the inner coordination of water. Both confirmed cases of Am(IV) were from the in-situ formation of strong chemical oxidizers.

Hobbs, D.; Visser, A.; Bridges, N.

2011-09-20T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

The use of ionic liquid ion sources (ILIS) in FIB applications  

E-Print Network [OSTI]

A new monoenergetic, high-brightness ion source can be constructed using an arrangement similar to liquid metal ion sources (LMIS) by substituting the liquid metal with an ionic liquid, or room temperature molten salt. Ion ...

Zorzos, Anthony Nicholas

2009-01-01T23:59:59.000Z

62

E-Print Network 3.0 - ammonium ionic liquids Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Atomic Data Center (CFADC) Collection: Plasma Physics and Fusion 2 "Control of protein folding and misfolding in ionic liquid media, and a conjecture on early earth biology"....

63

Methods of using ionic liquids having a fluoride anion as solvents  

DOE Patents [OSTI]

A method in one embodiment includes contacting a strongly hydrogen bonded organic material with an ionic liquid having a fluoride anion for solubilizing the strongly hydrogen bonded organic material; and maintaining the ionic liquid at a temperature of about 90.degree. C. or less during the contacting. A method in another embodiment includes contacting a strongly hydrogen bonded organic material with an ionic liquid having an acetate or formate anion for solubilizing the strongly hydrogen bonded organic material; and maintaining the ionic liquid at a temperature of less than about 90.degree. C. during the contacting.

Pagoria, Philip (Livermore, CA); Maiti, Amitesh (San Ramon, CA); Gash, Alexander (Brentwood, CA); Han, Thomas Yong (Pleasanton, CA); Orme, Christine (Oakland, CA); Fried, Laurence (Livermore, CA)

2011-12-06T23:59:59.000Z

64

Regenerating cellulose from ionic liquids for an accelerated enzymatic hydrolysis  

SciTech Connect (OSTI)

The efficient conversion of lignocellulosic materials into fuel ethanol has become a research priority in producing affordable and renewable energy. The pretreatment of lignocelluloses is known to be key to the fast enzymatic hydrolysis of cellulose. Recently, certain ionic liquids (ILs)were found capable of dissolving more than 10 wt% cellulose. Preliminary investigations [Dadi, A.P., Varanasi, S., Schall, C.A., 2006. Enhancement of cellulose saccharification kinetics using an ionic liquid pretreatment step. Biotechnol. Bioeng. 95, 904 910; Liu, L., Chen, H., 2006. Enzymatic hydrolysis of cellulose materials treated with ionic liquid [BMIM]Cl. Chin. Sci. Bull. 51, 2432 2436; Dadi, A.P., Schall, C.A., Varanasi, S., 2007. Mitigation of cellulose recalcitrance to enzymatic hydrolysis by ionic liquid pretreatment. Appl. Biochem. Biotechnol. 137 140, 407 421] suggest that celluloses regenerated from IL solutions are subject to faster saccharification than untreated substrates. These encouraging results offer the possibility of using ILs as alternative and nonvolatile solvents for cellulose pretreatment. However, these studies are limited to two chloride-based ILs: (a) 1-butyl-3-methylimidazolium chloride ([BMIM]Cl), which is a corrosive, toxic and extremely hygroscopic solid (m.p. 70 C), and (b) 1-allyl-3-methylimidazolium chloride ([AMIM]Cl), which is viscous and has a reactive side-chain. Therefore, more in-depth research involving other ILs is much needed to explore this promising pretreatment route. For this reason, we studied a number of chloride- and acetate-based ILs for cellulose regeneration, including several ILs newly developed in our laboratory. This will enable us to select inexpensive, efficient and environmentally benign solvents for processing cellulosic biomass. Our data confirm that all regenerated celluloses are less crystalline (58 75% lower) and more accessible to cellulase (>2 times) than untreated substrates. As a result, regenerated Avicel cellulose, filter paper and cottonwere hydrolyzed 2 10 times faster than the respective untreated celluloses. A complete hydrolysis of Avicel cellulose could be achieved in 6 h given the Trichoderma reesei cellulase/substrate ratio (w/w) of 3:20 at 50 C. In addition,we observed that cellulase is more thermally stable (up to 60 C) in the presence of regenerated cellulose. Furthermore, our systematic studies suggest that the presence of various ILs during the hydrolysis induced different degrees of cellulase inactivation. Therefore, a thorough removal of IL residues after cellulose regeneration is highly recommended, and a systematic investigation on this subject is much needed.

Zhao, Hua [Savannah State University; Jones, Cecil L [Savannah State University; Baker, Gary A [ORNL; Xia, Shuqian [Tianjin University, Tianjin, China; Olubajo, Olarongbe [Savannah State University; Person, Vernecia [Savannah State University

2009-01-01T23:59:59.000Z

65

Hydrogen Fluoride Capture by Imidazolium Acetate Ionic Liquid  

E-Print Network [OSTI]

Extraction of hydrofluoric acid (HF) from oils is a drastically important problem in petroleum industry, since HF causes quick corrosion of pipe lines and brings severe health problems to humanity. Some ionic liquids (ILs) constitute promising scavenger agents thanks to strong binding to polar compounds and tunability. PM7-MD simulations and hybrid density functional theory are employed here to consider HF capture ability of ILs. Discussing the effects and impacts of the cation and the anion separately and together, I will evaluate performance of imidazolium acetate and outline systematic search guidelines for efficient adsorption and extraction of HF.

Chaban, Vitaly

2015-01-01T23:59:59.000Z

66

Using Ionic Liquids in Selective Hydrocarbon Conversion Processes  

SciTech Connect (OSTI)

This is the Final Report of the five-year project Using Ionic Liquids in Selective Hydrocarbon Conversion Processes (DE-FC36-04GO14276, July 1, 2004- June 30, 2009), in which we present our major accomplishments with detailed descriptions of our experimental and theoretical efforts. Upon the successful conduction of this project, we have followed our proposed breakdown work structure completing most of the technical tasks. Finally, we have developed and demonstrated several optimized homogenously catalytic methane conversion systems involving applications of novel ionic liquids, which present much more superior performance than the Catalytica system (the best-to-date system) in terms of three times higher reaction rates and longer catalysts lifetime and much stronger resistance to water deactivation. We have developed in-depth mechanistic understandings on the complicated chemistry involved in homogenously catalytic methane oxidation as well as developed the unique yet effective experimental protocols (reactors, analytical tools and screening methodologies) for achieving a highly efficient yet economically feasible and environmentally friendly catalytic methane conversion system. The most important findings have been published, patented as well as reported to DOE in this Final Report and our 20 Quarterly Reports.

Tang, Yongchun; Periana, Roy; Chen, Weiqun; van Duin, Adri; Nielsen, Robert; Shuler, Patrick; Ma, Qisheng; Blanco, Mario; Li, Zaiwei; Oxgaard, Jonas; Cheng, Jihong; Cheung, Sam; Pudar, Sanja

2009-09-28T23:59:59.000Z

67

Interactions of Ionic Liquids with Uranium and its Bioreduction  

SciTech Connect (OSTI)

We investigated the influence of ionic liquids (ILs) 1-butyl-3-methylimidazolium hexafluorophosphate [BMIM]{sup +}[PF{sub 6}]{sup -}, N-ethylpyridinium trifluoroacetate [EtPy]{sup +}[CF{sub 3}COO]{sup -} and N-ethylpyridinium tetrafluoroborate [Et-Py]{sup +}[BF{sub 4}]{sup -} on uranium reduction by Clostridium sp. under anaerobic conditions. Potentiometric titration, UV-vis spectrophotometry, LC-MS and EXAFS analyses showed monodentate complexation between uranyl and BF{sub 4}{sup -} PF{sub 6}{sup -}; and bidentate complexation with CF{sub 3}COO{sup -}. Ionic liquids affected the growth of Clostridium sp. as evidenced by decrease in optical density, changes in pH, gas production, and the extent of U(VI) reduction and precipitation of U(IV) from solution. Reduction of U(VI) to U(IV) was observed in the presence of [EtPy][BF{sub 4}] and [BMIM][PF{sub 6}] but not with [EtPy][CF{sub 3}COO].

Zhang, C.; Francis, A.

2012-09-18T23:59:59.000Z

68

Development of an Ionic-Liquid Absorption Heat Pump  

SciTech Connect (OSTI)

Solar Fueled Products (SFP) is developing an innovative ionic-liquid absorption heat pump (ILAHP). The development of an ILAHP is extremely significant, as it could result in annual savings of more than 190 billion kW h of electrical energy and $19 billion. This absorption cooler uses about 75 percent less electricity than conventional cooling and heating units. The ILAHP also has significant environmental sustainability benefits, due to reduced CO2 emissions. Phase I established the feasibility and showed the economic viability of an ILAHP with these key accomplishments: • Used the breakthrough capabilities provided by ionic liquids which overcome the key difficulties of the common absorption coolers. • Showed that the theoretical thermodynamic performance of an ILAHP is similar to existing absorption-cooling systems. • Established that the half-effect absorption cycle reduces the peak generator temperature, improving collector efficiency and reducing collector area. • Component testing demonstrated that the most critical components, absorber and generator, operate well with conventional heat exchangers. • Showed the economic viability of an ILAHP. The significant energy savings, sustainability benefits, and economic viability are compelling reasons to continue the ILAHP development.

Holcomb, Don

2011-03-29T23:59:59.000Z

69

Method of purifying a gas stream using 1,2,3-triazolium ionic liquids  

DOE Patents [OSTI]

A method for separating a target gas from a gaseous mixture using 1,2,3-triazolium ionic liquids is presented. Industrial effluent streams may be cleaned by removing carbon dioxide from the stream by contacting the effluent stream with a 1,2,3-triazolium ionic liquid compound.

Luebke, David; Nulwala, Hunald; Tang, Chau

2014-12-09T23:59:59.000Z

70

Short Communication Bioreduction and precipitation of uranium in ionic liquid aqueous  

E-Print Network [OSTI]

with uranium from mining and milling operations, radioactive wastes, and from nuclear accidents is a majorShort Communication Bioreduction and precipitation of uranium in ionic liquid aqueous solution t s Uranium forms various complexes with ionic liquids. Uranium bioreduction was affected by the type

Ohta, Shigemi

71

Metal-air cell comprising an electrolyte with a room temperature ionic liquid and hygroscopic additive  

DOE Patents [OSTI]

An electrochemical cell comprising an electrolyte comprising water and a hydrophobic ionic liquid comprising positive ions and negative ions. The electrochemical cell also includes an air electrode configured to absorb and reduce oxygen. A hydrophilic or hygroscopic additive modulates the hydrophobicity of the ionic liquid to maintain a concentration of the water in the electrolyte is between 0.001 mol % and 25 mol %.

Friesen, Cody A.; Krishnan, Ramkumar; Tang, Toni; Wolfe, Derek

2014-08-19T23:59:59.000Z

72

Ionic Liquids: Radiation Chemistry, Solvation Dynamics and Reactivity Patterns  

SciTech Connect (OSTI)

Ionic liquids (ILs) are a rapidly expanding family of condensed-phase media with important applications in energy production, nuclear fuel and waste processing, improving the efficiency and safety of industrial chemical processes, and pollution prevention. ILs generally have low volatilities and are combustion-resistant, highly conductive, recyclable and capable of dissolving a wide variety of materials. They are finding new uses in chemical synthesis, catalysis, separations chemistry, electrochemistry and other areas. Ionic liquids have dramatically different properties compared to conventional molecular solvents, and they provide a new and unusual environment to test our theoretical understanding of primary radiation chemistry, charge transfer and other reactions. We are interested in how IL properties influence physical and dynamical processes that determine the stability and lifetimes of reactive intermediates and thereby affect the courses of reactions and product distributions. We study these issues by characterization of primary radiolysis products and measurements of their yields and reactivity, quantification of electron solvation dynamics and scavenging of electrons in different states of solvation. From this knowledge we wish to learn how to predict radiolytic mechanisms and control them or mitigate their effects on the properties of materials used in nuclear fuel processing, for example, and to apply IL radiation chemistry to answer questions about general chemical reactivity in ionic liquids that will aid in the development of applications listed above. Very early in our radiolysis studies it became evident that the slow solvation dynamics of the excess electron in ILs (which vary over a wide viscosity range) increase the importance of pre-solvated electron reactivity and consequently alter product distributions and subsequent chemistry. This difference from conventional solvents has profound effects on predicting and controlling radiolytic yields, which need to be quantified for the successful use under radiolytic conditions. Electron solvation dynamics in ILs are measured directly when possible and estimated using proxies (e.g. coumarin-153 dynamic emission Stokes shifts or benzophenone anion solvation) in other cases. Electron reactivity is measured using ultrafast kinetics techniques for comparison with the solvation process.

Wishart, J.F.

2011-06-12T23:59:59.000Z

73

Department of Energy and Mineral Engineering Spring 2013 Preliminary Plant Design For Bitumen Separation Using Ionic Liquid  

E-Print Network [OSTI]

For Bitumen Separation Using Ionic Liquid Overview IL Fuels LLC invented a novel way to separate bitumen from of producing 5,000 barrels of bitumen per day while maximizing the recovery of ionic liquid and water of bitumen/day Maintain a maximum of 0.2% loss of ionic liquids to the cleaned sands Improve overall

Demirel, Melik C.

74

The acoustical flows of the hydrophobic and anticeptic liquids in porous media  

E-Print Network [OSTI]

of the acoustical flows in the porous or microcrum- bling media. Concrete and brick walls being porous media absorbThe acoustical flows of the hydrophobic and anticeptic liquids in porous media V. Tsaplev North effect. Just the same, if the protective covering of the concrete or brick wall is damaged, they begin

Boyer, Edmond

75

Extraction of Biofuels and Biofeedstocks from Aqueous Solutions Using Ionic Liquids  

E-Print Network [OSTI]

Extraction of Biofuels and Biofeedstocks from Aqueous Solutions Using Ionic Liquids Luke D. Simoni-Butanol, Extraction, Liquid-Liquid Equilibrium, Excess Gibbs Energy Models, Biofuels #12;1 1. Introduction other organic compounds can be produced biologically, and thus can be considered as biofuel candidates

Stadtherr, Mark A.

76

Project Profile: Thermally-Stable Ionic Liquid Carriers forNanopartic...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

and Awards A. Visser, N. Bridges, E.B. Fox, J. Gray, and B. Garcia-Diaz, "Thermal and Corrosion Properties of Nanoparticle Enhanced Ionic Liquids (NEILs)," Prepr. Pap.-Am. Chem....

77

High Temperature/Low Humidity Polymer Electrolytes Derived from Ionic Liquids  

Broader source: Energy.gov [DOE]

Presentation on High Temperature/Low Humidity Polymer Electrolytes Derived from Ionic Liquids to the High Temperature Membrane Working Group Meeting held in Arlington, Virginia, May 26,2005.

78

Theoretical Investigations on Nanoporpus Materials and Ionic Liquids for Energy Storage  

E-Print Network [OSTI]

by adsorption. In this regard carbon nanotube and Metal Organic Framework (MOFs) based materials are worth studying. Ionic liquids (IL) are potential electrolytes that can improve energy storage capacity and safety in Li ion batteries. Therefore it is important...

Mani Biswas, Mousumi

2012-02-14T23:59:59.000Z

79

81929 - Fission-Product Separation Based on Room - Temperature Ionic Liquids  

SciTech Connect (OSTI)

This project has demonstrated that Sr2+ and Cs+ can be selectively extracted from aqueous solutions into ionic liquids using crown ethers and that unprecedented large distribution coefficients can be achieved for these fission products. The volume of secondary wastes can be significantly minimized with this new separation technology. Through the current EMSP funding, the solvent extraction technology based on ionic liquids has been shown to be viable and can potentially provide the most efficient separation of problematic fission products from high level wastes. The key results from the current funding period are the development of highly selective extraction process for cesium ions based on crown ethers and calixarenes, optimization of selectivities of extractants via systematic change of ionic liquids, and investigation of task-specific ionic liquids incorporating both complexant and solvent characteristics.

Robin D. Rogers

2004-12-09T23:59:59.000Z

80

Complex Capacitance Scaling in Ionic Liquids-Filled Nanopores  

SciTech Connect (OSTI)

Recent experiments have shown that the capacitance of subnanometer pores increases anomalously as the pore width decreases, thereby opening a new avenue for developing supercapacitors with enhanced energy density. However, this behavior is still subject to some controversy since its physical origins are not well understood. Using atomistic simulations, we show that the capacitance of slit-shaped nanopores in contact with room-temperature ionic liquids exhibits a U-shaped scaling behavior in pores with widths from 0.75 to 1.26 nm. The left branch of the capacitance scaling curve directly corresponds to the anomalous capacitance increase and thus reproduces the experimental observations. The right branch of the curve indirectly agrees with experimental findings that so far have received little attention. The overall U-shaped scaling behavior provides insights on the origins of the difficulty in experimentally observing the pore-width-dependent capacitance. We establish a theoretical framework for understanding the capacitance of electrical double layers in nanopores and provide mechanistic details into the origins of the observed scaling behavior. The framework highlights the critical role of 'ion solvation' in controlling pore capacitance and the importance of choosing anion/cation couples carefully for optimal energy storage in a given pore system.

Sumpter, Bobby G [ORNL

2011-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

Complex Capacitance Scaling in Ionic Liquids-filled Nanopores  

SciTech Connect (OSTI)

Recent experiments have shown that the capacitance of sub-nanometer pores increases anomalously as the pore width decreases, thereby opening a new avenue for developing supercapacitors with enhanced energy density. However, this behavior is still subject to some controversy since its physical origins are not well understood. Using atomistic simulations, we show that the capacitance of slit-shaped nanopores in contact with room-temperature ionic liquids exhibits a U-shaped scaling behavior in pores with width from 0.75 to 1.26 nm. The left branch of the capacitance scaling curve directly corresponds to the anomalous capacitance increase and thus reproduces the experimental observations. The right branch of the curve indirectly agrees with experimental findings that so far have received little attention. The overall U-shaped scaling behavior provides insights on the origins of the difficulty in experimentally observing the pore-width dependent capacitance. We establish a theoretical framework for understanding the capacitance of electrical double layers in nanopores and provide mechanistic details into the origins of the observed scaling behavior. The framework highlights the critical role of ion solvation in controlling pore capacitance and the importance of choosing anion/cation couples carefully for optimal energy storage in a given pore system.

Qiao, Rui [Clemson University; Huang, Jingsong [ORNL; Meunier, Vincent [ORNL; Sumpter, Bobby G [ORNL; Peng, Wu [Clemson University

2011-01-01T23:59:59.000Z

82

EFFECTS OF GAMMA RADIATION ON ELECTROCHEMICAL PROPERTIES OF IONIC LIQUIDS  

SciTech Connect (OSTI)

The electrochemical properties of ionic liquids (ILs) make them attractive for possible replacement of inorganic salts in high temperature molten salt electrochemical processing of nuclear fuel. To be a feasible replacement solvent, ILs need to be stable in moderate and high doses of radiation without adverse chemical and physical effects. Here, we exposed seven different ILs to a 1.2 MGy dose of gamma radiation to investigate their physical and chemical properties as they related to radiological stability. The azolium-based ILs experienced the greatest change in appearance, but these ILs were chemically more stable to gamma radiation than some of the other classes of ILs tested, due to the presence of aromatic electrons in the azolium ring. All the ILs exhibited a decrease in their conductivity and electrochemical window (at least 1.1 V), both of which could affect the utility of ILs in electrochemical processing. The concentration of the irradiation decomposition products was less than 3 mole %, with no impurities detectable using NMR techniques.

Visser, A; Nicholas Bridges, N; Thad Adams, T; John Mickalonis, J; Mark02 Williamson, M

2009-04-21T23:59:59.000Z

83

Interfacial Ionic Liquids: Connecting Static and Dynamic Structures  

E-Print Network [OSTI]

It is well-known that room temperature ionic liquids (RTILs) often adopt a charge-separated layered structure, i.e., with alternating cation- and anion-rich layers, at electrified interfaces. However, the dynamic response of the layered structure to temporal variations in applied potential is not well understood. We used in situ, real-time X-ray reflectivity (XR) to study the potential-dependent electric double layer (EDL) structure of an imidazolium-based RTIL on charged epitaxial graphene during potential cycling as a function of temperature. The results suggest that the graphene-RTIL interfacial structure is bistable in which the EDL structure at any intermediate potential can be described by the combination of two extreme-potential structures whose proportions vary depending on the polarity and magnitude of the applied potential. This picture is supported by the EDL structures obtained by fully atomistic molecular dynamics (MD) simulations at various static potentials. The potential-driven transition between the two structures is characterized by an increasing width but with an approximately fixed hysteresis magnitude as a function of temperature. The results are consistent with the coexistence of distinct anion and cation adsorbed structures separated by an energy barrier (~0.15 eV).

Ahmet Uysal; Hua Zhou; Guang Feng; Sang Soo Lee; Song Li; Peter T. Cummings; Pasquale F. Fulvio; Sheng Dai; John K. McDonough; Yury Gogotsi; Paul Fenter

2014-12-06T23:59:59.000Z

84

Temperature dependence of some liquid lithium properties from the ionic pseudopotential  

E-Print Network [OSTI]

OF SCIEECE May 1977 Ma)or Sub)ect: Mnclear Engineering TEMPERATURE DEPENDENCE OP SOME LIQUID LITHIUM PROPERTIES PROM THE IONIC PSEUDOPOTENTIAL A Thesis by ANTHONY WELLS ENGEL Approved as to style and content by: ea o spar men em er em er May 1977... ABSTRACT Temperature Dependence of Some Liquid Lithium Properties from the Ionic Pseudopotential. (May 1977) Anthony Wells Engely A B y Rutgers University Chairman of Advisory Committee: Dr. Henri R. Ieribaux The purpose of this investigation...

Engel, Anthony Wells

1977-01-01T23:59:59.000Z

85

Elucidating graphene - Ionic Liquid interfacial region: a combined experimental and computational study  

SciTech Connect (OSTI)

The interfacial region between graphene and an imidazolium based ionic liquid is studied using spectroscopic analysis and computational modelling. This combined approach reveals that the molecular level structure of the interfacial region is significantly influenced by functional group defects on the graphene surface.The combined experimental and computational study reveals that the molecular structure at interfacial region between graphene and imidazolium based ionic liquid is defined by the hydroxyl functional groups on the graphene surface

Vijayakumar, M.; Schwenzer, Birgit; Shutthanandan, V.; Hu, Jian Z.; Liu, Jun; Aksay, Ilhan A.

2014-01-10T23:59:59.000Z

86

DEVELOPMENT AND SELECTION OF IONIC LIQUID ELECTROLYTES FOR HYDROXIDE CONDUCTING POLYBENZIMIDAZOLE MEMBRANES IN ALKALINE FUEL CELLS  

SciTech Connect (OSTI)

Alkaline fuel cell (AFC) operation is currently limited to specialty applications such as low temperatures and pure H{sub 2}/O{sub 2} due to the corrosive nature of the electrolyte and formation of carbonates. AFCs are the cheapest and potentially most efficient (approaching 70%) fuel cells. The fact that non-Pt catalysts can be used, makes them an ideal low cost alternative for power production. The anode and cathode are separated by and solid electrolyte or alkaline porous media saturated with KOH. However, CO{sub 2} from the atmosphere or fuel feed severely poisons the electrolyte by forming insoluble carbonates. The corrosivity of KOH (electrolyte) limits operating temperatures to no more than 80?C. This chapter examines the development of ionic liquids electrolytes that are less corrosive, have higher operating temperatures, do not chemically bond to CO{sub 2}, and enable alternative fuels. Work is detailed on the IL selection and characterization as well as casting methods within the polybenzimidazole based solid membrane. This approach is novel as it targets the root of the problem (the electrolyte) unlike other current work in alkaline fuel cells which focus on making the fuel cell components more durable.

Fox, E.

2012-05-01T23:59:59.000Z

87

Ionic Liquids as Novel Lubricants and /or Lubricant Additives  

SciTech Connect (OSTI)

This ORNL-GM CRADA developed ionic liquids (ILs) as novel lubricants or oil additives for engine lubrication. A new group of oil-miscible ILs have been designed and synthesized with high thermal stability, non-corrosiveness, excellent wettability, and most importantly effective anti-scuffing/anti-wear and friction reduction characteristics. Mechanistic analysis attributes the superior lubricating performance of IL additives to their physical and chemical interactions with metallic surfaces. Working with a leading lubricant formulation company, the team has successfully developed a prototype low-viscosity engine oil using a phosphonium-phosphate IL as an anti-wear additive. Tribological bench tests of the IL-additized formulated oil showed 20-33% lower friction in mixed and elastohydrodynamic lubrication and 38-92% lower wear in boundary lubrication when compared with commercial Mobil 1 and Mobil Clean 5W-30 engine oils. High-temperature, high load (HTHL) full-size engine tests confirmed the excellent anti-wear performance for the IL-additized engine oil. Sequence VID engine dynamometer tests demonstrated an improved fuel economy by >2% for this IL-additized engine oil benchmarked against the Mobil 1 5W-30 oil. In addition, accelerated catalyst aging tests suggest that the IL additive may potentially have less adverse impact on three-way catalysts compared to the conventional ZDDP. Follow-on research is needed for further development and optimization of IL chemistry and oil formulation to fully meet ILSAC GF-5 specifications and further enhance the automotive engine efficiency and durability.

Qu, J. [ORNL; Viola, M. B. [General Motors Company

2013-10-31T23:59:59.000Z

88

Porous material and process development for electrospray propulsion applications  

E-Print Network [OSTI]

Ion electrospray propulsion devices rely on the transportation of ionic liquid propellant to emission regions where ions are extracted at high velocities. One such method involves the use of porous substrates to passively ...

Arestie, Steven Mark

2014-01-01T23:59:59.000Z

89

Studies of ionic liquids in lithium-ion battery test systems  

SciTech Connect (OSTI)

In this work, thermal and electrochemical properties of neat and mixed ionic liquid - lithium salt systems have been studied. The presence of a lithium salt causes both thermal and phase-behavior changes. Differential scanning calorimeter DSC and thermal gravimetric analysis TGA were used for thermal analysis for several imidazolium bis(trifluoromethylsulfonyl)imide, trifluoromethansulfonate, BF{sub 4}, and PF{sub 6} systems. Conductivities and diffusion coefficient have been measured for some selected systems. Chemical reactions in electrode - ionic liquid electrolyte interfaces were studied by interfacial impedance measurements. Lithium-lithium and lithium-carbon cells were studied at open circuit and a charged system. The ionic liquids studied include various imidazolium systems that are already known to be electrochemically unstable in the presence of lithium metal. In this work the development of interfacial resistance is shown in a Li|BMIMBF{sub 4} + LiBF{sub 4}|Li cell as well as results from some cycling experiments. As the ionic liquid reacts with the lithium electrode the interfacial resistance increases. The results show the magnitude of reactivity due to reduction of the ionic liquid electrolyte that eventually has a detrimental effect on battery performance.

Salminen, Justin; Prausnitz, John M.; Newman, John

2006-06-01T23:59:59.000Z

90

Structure and phase transitions into ionic adsorption layers on liquid interfaces  

E-Print Network [OSTI]

The structure of ionic adsorption layers is studied via a proper thermodynamic treatment of the electrostatic and non-electrostatic interactions between the surfactant ions as well as of the effect of thermodynamic non-locality. The analysis is also applied to phase transitions into the ionic adsorption layer, which interfere further with the oscillatory-diffusive structure of the electric double layer and hydrodynamic stability of squeezing waves in thin liquid films.

R. Tsekov

2014-10-25T23:59:59.000Z

91

Catalytic Conversion of Biomass to Fuels and Chemicals Using Ionic Liquids  

SciTech Connect (OSTI)

This project provides critical innovations and fundamental understandings that enable development of an economically-viable process for catalytic conversion of biomass (sugar) to 5-hydroxymethylfurfural (HMF). A low-cost ionic liquid (Cyphos 106) is discovered for fast conversion of fructose into HMF under moderate reaction conditions without any catalyst. HMF yield from fructose is almost 100% on the carbon molar basis. Adsorbent materials and adsorption process are invented and demonstrated for separation of 99% pure HMF product and recovery of the ionic liquid from the reaction mixtures. The adsorbent material appears very stable in repeated adsorption/regeneration cycles. Novel membrane-coated adsorbent particles are made and demonstrated to achieve excellent adsorption separation performances at low pressure drops. This is very important for a practical adsorption process because ionic liquids are known of high viscosity. Nearly 100% conversion (or dissolution) of cellulose in the catalytic ionic liquid into small molecules was observed. It is promising to produce HMF, sugars and other fermentable species directly from cellulose feedstock. However, several gaps were identified and could not be resolved in this project. Reaction and separation tests at larger scales are needed to minimize impacts of incidental errors on the mass balance and to show 99.9% ionic liquid recovery. The cellulose reaction tests were troubled with poor reproducibility. Further studies on cellulose conversion in ionic liquids under better controlled conditions are necessary to delineate reaction products, dissolution kinetics, effects of mass and heat transfer in the reactor on conversion, and separation of final reaction mixtures.

Liu, Wei; Zheng, Richard; Brown, Heather; Li, Joanne; Holladay, John; Cooper, Alan; Rao, Tony; ,

2012-04-13T23:59:59.000Z

92

High-Pressure Phase Equilibria of Ionic Liquids and Compressed Gases for Applications in Reactions and Absorption Refrigeration  

E-Print Network [OSTI]

of high-melting solids not liquids at processing conditions. Coupling ionic liquids with compressed gases systems may overcome most of these difficulties for their applications in separations, reactions, materials processing and engineering applications...

Ren, Wei

2009-12-29T23:59:59.000Z

93

Ionic liquids and ionic liquid acids with high temperature stability for fuel cell and other high temperature applications, method of making and cell employing same  

DOE Patents [OSTI]

Disclosed are developments in high temperature fuel cells including ionic liquids with high temperature stability and the storage of inorganic acids as di-anion salts of low volatility. The formation of ionically conducting liquids of this type having conductivities of unprecedented magnitude for non-aqueous systems is described. The stability of the di-anion configuration is shown to play a role in the high performance of the non-corrosive proton-transfer ionic liquids as high temperature fuel cell electrolytes. Performance of simple H.sub.2(g) electrolyte/O.sub.2(g) fuel cells with the new electrolytes is described. Superior performance both at ambient temperature and temperatures up to and above 200.degree. C. are achieved. Both neutral proton transfer salts and the acid salts with HSO.sup.-.sub.4 anions, give good results, the bisulphate case being particularly good at low temperatures and very high temperatures. The performance of all electrolytes is improved by the addition of a small amount of involatile base of pK.sub.a value intermediate between those of the acid and base that make the bulk electrolyte. The preferred case is the imidazole-doped ethylammonium hydrogensulfate which yields behavior superior in all respects to that of the industry standard phosphoric acid electrolyte.

Angell, C. Austen (Mesa, AZ); Xu, Wu (Broadview Heights, OH); Belieres, Jean-Philippe (Chandler, AZ); Yoshizawa, Masahiro (Tokyo, JP)

2011-01-11T23:59:59.000Z

94

Method to prepare nanoparticles on porous mediums  

DOE Patents [OSTI]

A method to prepare porous medium decorated with nanoparticles involves contacting a suspension of nanoparticles in an ionic liquid with a porous medium such that the particles diffuse into the pores of the medium followed by heating the resulting composition to a temperature equal to or greater than the thermal decomposition temperature of the ionic liquid resulting in the removal of the liquid portion of the suspension. The nanoparticles can be a metal, an alloy, or a metal compound. The resulting compositions can be used as catalysts, sensors, or separators.

Vieth, Gabriel M. (Knoxville, TN) [Knoxville, TN; Dudney, Nancy J. (Oak Ridge, TN) [Oak Ridge, TN; Dai, Sheng (Knoxville, TN) [Knoxville, TN

2010-08-10T23:59:59.000Z

95

Towards In situ extraction of fine chemicals and biorenewable fuels from fermentation broths using Ionic liquids and the Intensification of contacting by the application of Electric Fields  

E-Print Network [OSTI]

and design new ionic liquids for task specific needs. Solvent selection for in situ fermentation is depended on high solute partitioning and their biocompatibility with the microorganisms. Such information for these new set of solvents, ionic liquids...

Gangu, Satya Aravind

2013-05-31T23:59:59.000Z

96

Electrochemical Polishing Applications and EIS of a Novel Choline Chloride-Based Ionic Liquid  

SciTech Connect (OSTI)

Minimal surface roughness is a critical feature for high-field superconducting radio frequency (SRF) cavities used to engineer particle accelerators. Current methods for polishing Niobium cavities typically utilize solutions containing a mixture of concentrated sulfuric and hydrofluoric acid. Polishing processes such as these are effective, yet there are many hazards and costs associated with the use (and safe disposal) of the concentrated acid solutions. An alternative method for electrochemical polishing of the cavities was explored using a novel ionic liquid solution containing choline chloride. Potentiostatic electrochemical impedance spectroscopy (EIS) was used to analyze the ionic polishing solution. Final surface roughness of the Nb was found to be comparable to that of the acid-polishing method, as assessed by atomic force microscopy (AFM). This indicates that ionic liquid-based electrochemical polishing of Nb is a viable replacement for acid-based methods for preparation of SRF cavities.

Wixtrom, Alex I. [Christopher Newport University, Newport News, VA (United States); Buhler, Jessica E. [Christopher Newport University, Newport News, VA (United States); Reece, Charles E. [Thomas Jefferson National Accelerator Facility, Newport News, VA (United States); Abdel-Fattah, Tarek M. [Christopher Newport University, Newport News, VA (United States)

2013-06-01T23:59:59.000Z

97

Reverse Atom Transfer Radical Polymerization of Methyl Methacrylate in Room-Temperature Ionic Liquids  

E-Print Network [OSTI]

, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China Received 14, the removal and recycling of the catalytic materials become important. It is expected that using ionic liquids as ATRP media. They performed the copper(I)-mediated ATRP of methyl methacrylate (MMA) in 1-butyl-3

Wan, Xin-hua

98

Ionic Liquids as templating agents in formation of uranium-containing nanomaterials  

SciTech Connect (OSTI)

A method for forming nanoparticles containing uranium oxide is described. The method includes combining a uranium-containing feedstock with an ionic liquid to form a mixture and holding the mixture at an elevated temperature for a period of time to form the product nanoparticles. The method can be carried out at low temperatures, for instance less than about 300.degree. C.

Visser, Ann E; Bridges, Nicholas J

2014-06-10T23:59:59.000Z

99

Use of polymer/ionic liquid plasticizers as gel electrolytes in electrochromic devices  

E-Print Network [OSTI]

Use of polymer/ionic liquid plasticizers as gel electrolytes in electrochromic devices H. Bircana polymer configuration is commonly used when constructing electrochromic devices (ECDs) due to the expected)thienyl)-N-methylcarbazole] (PBEDOT-NMCz) as the two complementary electrochromic polymers for the device. A variety of gel

Otero, Toribio Fernández

100

Physicochemical properties of 1,2,3-triazolium ionic liquids{ Shilpi Sanghi,a  

E-Print Network [OSTI]

Versek,b Mark Tuominenb and E. Bryan Coughlin*a Received 8th June 2011, Accepted 26th October 2011 DOI liquids including ion cluster behavior, thermal properties, electrochemical stability and ionic hydroxide ion at 80 uC was studied. Key features of 1,2,3-triazolium salts are their high electrochemical

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


101

Protein Unfolding, and the "Tuning In" of Reversible Intermediate States, in Protic Ionic Liquid Media  

E-Print Network [OSTI]

's heat capacity as it undergoes the unfolding process. This yields a spe- cific enthalpy change, which partial heat capacities, we will simply report the total system heat capacity and attribute the partProtein Unfolding, and the "Tuning In" of Reversible Intermediate States, in Protic Ionic Liquid

Angell, C. Austen

102

The Role of Confined Water in Ionic Liquid Electrolytes for Dye-Sensitized Solar Cells  

E-Print Network [OSTI]

The Role of Confined Water in Ionic Liquid Electrolytes for Dye- Sensitized Solar Cells Jiwon Jeon %) for applications such as nonvolatile electrolytes for dye-sensitized solar cells (DSSCs). This suggests a strategy Structure, Quantum Chemistry,General Theory The dye-sensitized solar cell (DSSC) proposed by Gratzel et al.1

Goddard III, William A.

103

Protic Ionic Liquids: Preparation, Characterization, and Proton Free Energy Level Representation  

E-Print Network [OSTI]

interesting properties, including the ability to serve as electrolytes in solvent-free fuel cell systems. We in a fuel cell.2,7,8 This is an application which requires the presence of a special type of ionic liquids continue to be found. They are the low-melting relatives of molten salts whose place in the history

Angell, C. Austen

104

A Comparison of Electron-Transfer Dynamics inIonic Liquids and Neutral Solvents  

SciTech Connect (OSTI)

The effect of ionic liquids on photoinduced electron-transfer reactions in a donor-bridge-acceptor system is examined for two ionic liquid solvents, 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)amide and tributylmethylammonium bis(trifluoromethylsulfonyl)amide. The results are compared with those for the same system in methanol and acetonitrile solution. Electron-transfer rates were measured using time-resolved fluorescence quenching for the donor-bridge-acceptor system comprising a 1-N,1-N-dimethylbenzene-1,4-diamine donor, a proline bridge, and a coumarin 343 acceptor. The photoinduced electron-transfer processes are in the inverted regime (-{Delta}G > {lambda}) in all four solvents, with driving forces of -1.6 to -1.9 eV and estimated reorganization energies of about 1.0 eV. The observed electron-transfer kinetics have broadly distributed rates that are generally slower in the ionic liquids compared to the neutral solvents, which also have narrower rate distributions. To describe the broad distributions of electron-transfer kinetics, we use two different models: a distribution of exponential lifetimes and a discrete sum of exponential lifetimes. Analysis of the donor-acceptor electronic coupling shows that for ionic liquids this intramolecular electron-transfer reaction should be treated using a solvent-controlled electron-transfer model.

Wishart J. F.; Lee, H.Y.; Issa, J.B.; Isied, S.S.; Castner, Jr., E.W.; Pan, Y.; Hussey, C.L.; Lee, K.S.

2012-03-01T23:59:59.000Z

105

Ionic Liquids as Novel Lubricant Additives for Next-Generation  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-SeriesFlickrinformation for andFuel-Efficient Engines | ornl.gov Ionic

106

J-aggregation of ionic liquid solutions of meso-tetrakis(4-sulfonatophenyl)porphyrin  

SciTech Connect (OSTI)

The title porphyrin was dissolved in the hydrophilic ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate, [bmim][BF4], and triggered to assemble into J-aggregates by the addition of incremental volumes of water containing various amounts of acid (0.1, 0.2, or 1.0 M HCl). In contrast to recent studies, the current investigation is unique in that it centers on media that contain a predominant ionic liquid component (2.9 5.4 M [bmim][BF4]), as opposed to an aqueous electrolyte containing a small fraction of ionic liquid as dissociated solute. Complex aggregation and underlying photophysical behavior are revealed from absorption spectroscopy, steady-state fluorescence, and resonance light scattering studies. Upon addition of aqueous HCl, the efficient formation of H4TPPS2 J-aggregates from the diprotonated form of meso-tetrakis(4-sulfonatophenyl)porphyrin (H2TPPS4) occurs in [bmim][BF4]-rich media in a manner highly dependent upon the acidity, TPPS concentration, and solvent composition. The unique features of TPPS aggregation in this ionic liquid were elucidated, including the surprising disassembly of J-aggregates at higher aqueous contents, and our results are described qualitatively in terms of the molecular exciton theory. Finally, the potential of this system for the optical sensing of water at a sensitivity below 0.5 wt% is demonstrated. Overall, our findings accentuate how little is known about functional self-assembly within ionic liquids and suggest a number of avenues for exploring this completely untouched research landscape.

Ali, Maroof [Indian Institute of Technology, Delhi; Kumar, Vinod [ORNL; Baker, Sheila N [ORNL; Baker, Gary A [ORNL; Pandey, Siddharth [Indian Institute of Technology, Delhi

2010-01-01T23:59:59.000Z

107

Ionic Liquids for Utilization of Waste Heat from Distributed Power Generation Systems  

SciTech Connect (OSTI)

The objective of this research project was the development of ionic liquids to capture and utilize waste heat from distributed power generation systems. Ionic Liquids (ILs) are organic salts that are liquid at room temperature and they have the potential to make fundamental and far-reaching changes in the way we use energy. In particular, the focus of this project was fundamental research on the potential use of IL/CO2 mixtures in absorption-refrigeration systems. Such systems can provide cooling by utilizing waste heat from various sources, including distributed power generation. The basic objectives of the research were to design and synthesize ILs appropriate for the task, to measure and model thermophysical properties and phase behavior of ILs and IL/CO2 mixtures, and to model the performance of IL/CO2 absorption-refrigeration systems.

Joan F. Brennecke; Mihir Sen; Edward J. Maginn; Samuel Paolucci; Mark A. Stadtherr; Peter T. Disser; Mike Zdyb

2009-01-11T23:59:59.000Z

108

Gas-liquid critical point in ionic fluids  

E-Print Network [OSTI]

Based on the method of collective variables we develop the statistical field theory for the study of a simple charge-asymmetric $1:z$ primitive model (SPM). It is shown that the well-known approximations for the free energy, in particular DHLL and ORPA, can be obtained within the framework of this theory. In order to study the gas-liquid critical point of SPM we propose the method for the calculation of chemical potential conjugate to the total number density which allows us to take into account the higher order fluctuation effects. As a result, the gas-liquid phase diagrams are calculated for $z=2-4$. The results demonstrate the qualitative agreement with MC simulation data: critical temperature decreases when $z$ increases and critical density increases rapidly with $z$.

O. Patsahan; I. Mryglod; T. Patsahan

2006-06-27T23:59:59.000Z

109

Extraction of Uranium from Aqueous Solutions Using Ionic Liquid and Supercritical Carbon Dioxide in Conjunction  

SciTech Connect (OSTI)

Uranyl ions (UO2)2+ in aqueous nitric acid solutions can be extracted into supercritical CO2 (sc-CO2) via an imidazolium-based ionic liquid using tri-n-butylphosphate (TBP) as a complexing agent. The transfer of uranium from the ionic liquid to the supercritical fluid phase was monitored by UV/Vis spectroscopy using a high-pressure fiberoptic cell. The form of the uranyl complex extracted into the supercritical CO2 phase was found to be UO2(NO3)2(TBP)2. The extraction results were confirmed by UV/Vis spectroscopy and by neutron activation analysis. This technique could potentially be used to extract other actinides for applications in the field of nuclear waste management.

Wang, Joanna S.; Sheaff, Chrystal N.; Yoon, Byunghoon; Addleman, Raymond S.; Wai, Chien M.

2009-01-01T23:59:59.000Z

110

Capacitive Energy Storage from - 50o to 100o Using an Ionic Liquid Electrolyte  

SciTech Connect (OSTI)

Relying on redox reactions, most batteries are limited in their ability to operate at very low or very high temperatures. While performance of electrochemical capacitors is less dependent on the temperature, present-day devices still cannot cover the entire range needed for automotive and electronics applications under a variety of environmental conditions. We show that the right combination of the exohedral nanostructured carbon (nanotubes and onions) electrode and a eutectic mixture of ionic liquids can dramatically extend the temperature range of electrical energy storage, thus defying the conventional wisdom that ionic liquids can only be used as electrolytes above room temperature. We demonstrate electrical double layer capacitors able to operate from 50 to 100 C over a wide voltage window (up to 3.7 V) and at very high charge/discharge rates of up to 20 V/s.

Lin, Rongying [Universite Paul Sabatier, Toulouse Cedex, France.; Taberna, Pierre-Louis [Universite Paul Sabatier, Toulouse Cedex, France.; Santini, Sebastien [SOLVIONIC Company, Toulouse, France; Presser, Volker [ORNL; Perez, Carlos R. [Drexel University; Malbosc, Francois [SOLVIONIC Company, Toulouse, France; Rupesinghe, Nalin L. [AIXTRON, Cambridge, UK; Teo, Kenneth B. K. [AIXTRON, Cambridge, UK; Gogotsi, Yury G. [Drexel University; Simon, Patrice [Universite Paul Sabatier, Toulouse Cedex, France.

2011-01-01T23:59:59.000Z

111

Anion effects in the extraction of lanthanide 2-thenoyltrifluoroacetone complexes into an ionic liquid  

SciTech Connect (OSTI)

The extraction of trivalent lanthanides from an aqueous phase containing 1 M NaClO{sub 4} into the room temperature ionic liquid 1-butyl-3-methylimidazolium nonafluoro-1-butane sulfonate by the beta-diketone extractant 2-thenoyltrifluoroacetone (Htta) was studied. Radiotracer distribution, absorption spectroscopy, time-resolved laser-induced fluorescence spectroscopy, and X-ray absorption fine structure measurements point to the extraction of multiple lanthanide species. At low extractant concentrations, fully hydrated aqua cations of the lanthanides are present in the ionic liquid phase. As the extractant concentration is increased 1:2 and 1:3 lanthanide:tta species are observed. In contrast, 1:4 Ln:tta complexes were observed in the extraction of lanthanides by Htta into 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide. (authors)

Jensen, Mark P.; Beitz, James V.; Rickert, Paul G. [Argonne Natl Lab, Chem Sci and Engn Div, Argonne, IL 60439 (United States); Borkowski, Marian [Argonne Natl Lab, Chem Sci and Engn Div, Argonne, IL 60439 (United States); Los Alamos Natl Lab, Earth and Environm Sci Div, Carlsbad, NM, (United States); Laszak, Ivan [Argonne Natl Lab, Chem Sci and Engn Div, Argonne, IL 60439 (United States); Commisariat Energie Atom, DEN DPC SERC LANIE, Gif Sur Yvette, (France); Dietz, Mark L. [Argonne Natl Lab, Chem Sci and Engn Div, Argonne, IL 60439 (United States); Wisconsin-Milwaukee Univ, Department of Chemistry and Biochemistry, Milwaukee, WI, (United States)

2012-07-01T23:59:59.000Z

112

Fabrication of hollow mesoporous NiO hexagonal microspheres via hydrothermal process in ionic liquid  

SciTech Connect (OSTI)

Highlights: Black-Right-Pointing-Pointer Ni(OH){sub 2} precursors were synthesized in ionic liquid and water solution by hydrothermal method. Black-Right-Pointing-Pointer NiO hollow microspheres were prepared by thermal treatment of Ni(OH){sub 2} precursors. Black-Right-Pointing-Pointer NiO hollow microspheres were self-assembled by mesoporous cubic and hexagonal nanocrystals with high specific surface area. Black-Right-Pointing-Pointer The mesoporous structure is stable at 773 K. Black-Right-Pointing-Pointer The ionic liquid absorbed on the O-terminate surface of the crystals to form hydrogen bond and played key roles in determining the final shape of the NiO novel microstructure. -- Abstract: The novel NiO hexagonal hollow microspheres have been successfully prepared by annealing Ni(OH){sub 2}, which was synthesized via an ionic liquid-assisted hydrothermal method. The samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM), N{sub 2} adsorption-desorption and Fourier transform infrared spectrometer (FTIR). The results show that the hollow NiO microstructures are self-organized by mesoporous cubic and hexagonal nanocrystals. The mesoporous structure possessed good thermal stability and high specific surface area (ca. 83 m{sup 2}/g). The ionic liquid 1-butyl-3methylimidazolium tetrafluoroborate ([Bmim][BF{sub 4}]) was found to play a key role in controlling the morphology of NiO microstructures during the hydrothermal process. The special hollow mesoporous architectures will have potential applications in many fields, such as catalysts, absorbents, sensors, drug-delivery carriers, acoustic insulators and supercapacitors.

Zhao, Jinbo, E-mail: zhaojinb@gmail.com [Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), Shandong University, 250061, Jinan (China) [Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), Shandong University, 250061, Jinan (China); School of Materials Science and Engineering, Shandong University, 250061, Jinan (China); Wu, Lili, E-mail: wulili@sdu.edu.cn [Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), Shandong University, 250061, Jinan (China) [Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), Shandong University, 250061, Jinan (China); School of Materials Science and Engineering, Shandong University, 250061, Jinan (China); Zou, Ke, E-mail: zouk2005@163.com [Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), Shandong University, 250061, Jinan (China) [Key Laboratory for Liquid-Solid Structural Evolution and Processing of Materials (Ministry of Education), Shandong University, 250061, Jinan (China); School of Materials Science and Engineering, Shandong University, 250061, Jinan (China)

2011-12-15T23:59:59.000Z

113

Liquid/Liquid Interface Polymerized Porphyrin Membranes Displaying Size-Selective Molecular and Ionic Permeability  

E-Print Network [OSTI]

Liquid/Liquid Interface Polymerized Porphyrin Membranes Displaying Size-Selective Molecular: December 5, 2005 Thin polymeric membranes have been formed by liquid/liquid interfacial copolymerization of controllable thickness to be obtained.7 The polymerization of 1 was accomplished by condensation of porphyrin

114

Checkerboard Self-Patterning of an Ionic Liquid Film on Mercury  

SciTech Connect (OSTI)

{angstrom}-resolution studies of room temperature ionic liquid (RTIL) interfaces are scarce, in spite of their long-recognized importance for the science and many applications of RTILs. We present an {angstrom}-resolution x-ray study of a Langmuir film of an RTIL on mercury. At low (high) coverage [90 (50) {angstrom}{sup 2}/molecule] a mono-(bi)layer of surface-parallel molecules is found. The molecules self-assemble in a lateral ionic checkerboard pattern, unlike the uniform-charge, alternate-ion layers of this RTIL at its bulk-solid interface. A 2D-smectic order is found, with molecules packed in parallel stripes, forming long-range order normal to, but none along, the stripes.

L Tamam; B Ocko; H Reichert; M Deutsch

2011-12-31T23:59:59.000Z

115

Checkerboard Self-Patterning of an Ionic Liquid Film on Mercury  

SciTech Connect (OSTI)

{angstrom}-resolution studies of room temperature ionic liquid (RTIL) interfaces are scarce, in spite of their long-recognized importance for the science and many applications of RTILs. We present an {angstrom}-resolution x-ray study of a Langmuir film of an RTIL on mercury. At low (high) coverage [90 (50) {angstrom}{sup 2}/molecule] a mono-(bi)layer of surface-parallel molecules is found. The molecules self-assemble in a lateral ionic checkerboard pattern, unlike the uniform-charge, alternate-ion layers of this RTIL at its bulk-solid interface. A 2D-smectic order is found, with molecules packed in parallel stripes, forming long-range order normal to, but none along, the stripes.

Ocko, B.M.; Tamam, L.; Reichert, H.; Deutsch, M.

2011-05-10T23:59:59.000Z

116

Squeezout phenomena and boundary layer formation of a model ionic liquid under confinement and charging  

E-Print Network [OSTI]

Electrical charging of parallel plates confining a model ionic liquid down to nanoscale distances yields a variety of charge-induced changes in the structural features of the confined film. That includes even-odd switching of the structural layering and charging-induced solidification and melting, with important changes of local ordering between and within layers, and of squeezout behavior. By means of molecular dynamics simulations, we explore this variety of phenomena in the simplest charged Lennard-Jones coarse-grained model including or excluding the effect a neutral tail giving an anisotropic shape to one of the model ions. Using these models and open conditions permitting the flow of ions in and out of the interplate gap, we simulate the liquid squeezout to obtain the distance dependent structure and forces between the plates during their adiabatic appraoch under load. Simulations at fixed applied force illustrate an effective electrical pumping of the ionic liquid, from a thick nearly solid film that withstands the interplate pressure for high plate charge to complete squeezout following melting near zero charge. Effective enthalpy curves obtained by integration of interplate forces versus distance show the local minima that correspond to layering, and predict the switching between one minimum and another under squeezing and charging.

R. Capozza; A. Vanossi; A. Benassi; E. Tosatti

2014-12-22T23:59:59.000Z

117

Reversible Ionic Liquids as Double-Action Solvents for Efficient CO2 Capture  

SciTech Connect (OSTI)

We have developed a novel class of CO{sub 2} capture solvents, Reversible Ionic Liquids (RevILs), that offer high absorption capacity through two modes of capture: chemical reaction (chemisorption) and physical solubility (physisorption). These solvents are silicon containing alkaline compounds such as silylamines that form a liquid salt (ionic liquid) upon reaction with CO{sub 2}. Subsequently, modest elevations in temperature reverse the reaction and yield pure CO{sub 2} for sequestration. By incorporating Si in the molecules we have reduced the viscosity, thereby improving the mass transfer rates of CO{sub 2} absorption/desorption and decreasing the processing costs for pumping the solvent. In this project, we have made systematic changes to the structure of these compounds to improve several physical and thermodynamic properties important for CO{sub 2} capture. Through these structure-property paradigms, we have obtained a RevIL which requires only a third of the energy required by conventional aqueous MEA process for 90% CO{sub 2} capture.

Eckert, Charles; Liotta, Charles

2011-09-30T23:59:59.000Z

118

Reversible Ionic Liquids as Double-Action Solvents for Efficient CO{sub 2} Capture  

SciTech Connect (OSTI)

We have developed a novel class of CO{sub 2} capture solvents, Reversible Ionic Liquids (RevILs), that offer high absorption capacity through two modes of capture: chemical reaction (chemisorption) and physical solubility (physisorption). These solvents are silicon containing alkaline compounds such as silylamines that form a liquid salt (ionic liquid) upon reaction with CO{sub 2}. Subsequently, modest elevations in temperature reverse the reaction and yield pure CO{sub 2} for sequestration. By incorporating Si in the molecules we have reduced the viscosity, thereby improving the mass transfer rates of CO{sub 2} absorption/desorption and decreasing the processing costs for pumping the solvent. In this project, we have made systematic changes to the structure of these compounds to improve several physical and thermodynamic properties important for CO{sub 2} capture. Through these structure-property paradigms, we have obtained a RevIL which requires only a third of the energy required by conventional aqueous MEA process for 90% CO{sub 2} capture.

Charles Eckert; Charles Liotta

2011-09-30T23:59:59.000Z

119

First evidence of anisotropic quenched disorder effects on a smectic liquid crystal confined in porous silicon  

E-Print Network [OSTI]

We present a neutron scattering analysis of the structure of the smectic liquid crystal octylcyanobiphenyl (8CB) confined in one-dimensional nanopores of porous silicon films (PS). The smectic transition is completely suppressed, leading to the extension of a short-range ordered smectic phase aligned along the pore axis. It evolves reversibly over an extended temperature range, down to 50 K below the \\textit{N-SmA} transition in pure 8CB. This behavior strongly differs from previous observations of smectics in different one-dimensional porous materials. A coherent picture of this striking behavior requires that quenched disorder effects are invoked. The strongly disordered nature of the inner surface of PS acts as random fields coupling to the smectic order. The one-dimensionality of PS nano-channels offers new perspectives on quenched disorder effects, which observation has been restricted to homogeneous random porous materials so far.

Régis Guégan; Denis Morineau; Claude Loverdo; Wilfried Béziel; Mohammed Guendouz

2005-11-08T23:59:59.000Z

120

Ionic Liquids: Breakthrough Absorption Technology for Post-Combustion CO{sub 2} Capture  

SciTech Connect (OSTI)

This is the final report for DE-FC26-07NT43091 â??Ionic Liquids: Breakthrough Absorption Technology for Post-Combustion CO{sub 2} Captureâ?. A detailed summary is provided of the ionic liquid (IL) discovery process, synthesis and testing results, process / systems modeling, lab-scale operational testing, corrosion testing and commercialization possibilities. The work resulted in the discovery of a new class of ionic liquids (ILs) that efficiently react with CO{sub 2} in a 1:1 stoichiometry with no water present and no increase in viscosity. The enthalpy of reaction was tuned to optimize process economics. The IL was found to have excellent corrosion behavior with and without CO{sub 2} present. In lab-scale tests, the IL was able to effectively remove CO{sub 2} from a simulated flue gas stream, although mass transfer was slower than with aqueous monoethanolamine (MEA) due to higher viscosities. The non-volatile nature of the solvent and its high thermal stability, however, make it an intriguing option. An independent systems analysis indicates that the economics of using the best IL discovered to date (NDIL0157), are at least comparable to â?? and potentially slightly better than -â?? the Fluor Econamine FG PlusTM process (DOE Case 12). Further work should be directed at improving mass transfer / lowering viscosity and developing commercial synthesis routes to make these ILs at scale in an inexpensive manner. Demonstration of the process at larger scales is also warranted, as is the exploration of other process configurations that leverage the anhydrous nature of the solvent and its extremely low volatility.

Maginn, Edward

2012-09-30T23:59:59.000Z

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121

THERMOPHYSICAL PROPERTIES OF NANOPARTICLE-ENHANCED IONIC LIQUIDS HEAT TRANSFER FLUIDS  

SciTech Connect (OSTI)

An experimental investigation was completed on nanoparticle enhanced ionic liquid heat transfer fluids as an alternative to conventional organic based heat transfer fluids (HTFs). These nanoparticle-based HTFs have the potential to deliver higher thermal conductivity than the base fluid without a significant increase in viscosity at elevated temperatures. The effect of nanoparticle morphology and chemistry on thermophysical properties was examined. Whisker shaped nanomaterials were found to have the largest thermal conductivity temperature dependence and were also less likely to agglomerate in the base fluid than spherical shaped nanomaterials.

Fox, E.

2013-04-15T23:59:59.000Z

122

Bias-dependent molecular-level structure of electrical double layer in ionic liquid on graphite  

SciTech Connect (OSTI)

Bias-dependent structure of electrochemical double layers at liquid-solid interfaces underpin a multitude of phenomena in virtually all areas of scientific enquiry ranging from energy storage and conversion systems, biology, to geophysics and geochemistry. Here we report the bias-evolution of the electric double layer structure of an ionic liquid on highly ordered pyrolytic graphite as a model system for carbon-based electrodes for electrochemical supercapacitors measured by atomic force microscopy. Matching the observed structures to molecular dynamics simulations allows us to resolve steric effects due to cation and anion layers. We observe reconfiguration under applied bias and the orientational transitions in the Stern layer. The synergy between molecular dynamics simulation and experiment provides a comprehensive picture of structural phenomena and long- and short range interactions. This insight will improve understanding of the mechanism of charge storage in electrochemical capacitors on a molecular level which can be used to enhance their electrochemical performance.

Black, Jennifer M [ORNL] [ORNL; Walters, Deron [Asylum Research, Santa Barbara, CA] [Asylum Research, Santa Barbara, CA; Labuda, Aleksander [Asylum Research, Santa Barbara, CA] [Asylum Research, Santa Barbara, CA; Feng, Guang [ORNL] [ORNL; Hillesheim, Patrick C [ORNL] [ORNL; Dai, Sheng [ORNL] [ORNL; Cummings, Peter T [ORNL] [ORNL; Kalinin, Sergei V [ORNL] [ORNL; Proksch, Roger [Asylum Research, Santa Barbara, CA] [Asylum Research, Santa Barbara, CA; Balke, Nina [ORNL] [ORNL

2013-01-01T23:59:59.000Z

123

A Preliminary Study of Oxidation of Lignin from Rubber Wood to Vanillin in Ionic Liquid Medium  

E-Print Network [OSTI]

In this study, lignin was oxidised to vanillin by means of oxygen in ionic liquid (1,3-dimethylimidazolium methylsulphate) medium. The parameters of the oxidation reaction that have been investigated were the following: concentration of oxygen (5, 10, 15 and 20 ft3 h-1), reaction time (2, 4, 6, 8 and 10 h) and reaction temperature (25, 40, 60, 80 and 100{\\deg}C). The Fourier transform infrared spectroscopy, high performance liquid chromatography and ultraviolet-visible analyses were used to characterise the product. The results revealed vanillin as the product obtained via the oxidation reaction. The optimum parameters of vanillin production were 20 ft3 h-1 of oxygen for 10 h at 100{\\deg}C. In conclusion, 1,3-dimethylimidazolium methylsulphate could be used as an oxidation reaction medium for the production of vanillin from rubber wood lignin.

Shamsuri, A A

2013-01-01T23:59:59.000Z

124

Conductivity of ionic liquid-derived polymers with internal gold nanoparticle conduits.  

SciTech Connect (OSTI)

The transport properties of self-supporting Au nanoparticle-ionic liquid-derived polymer composites were characterized. Topographic AFM images confirm the perforated lamellar composite architecture determined by small-angle X-ray scattering (SAXS) and further show that the in situ synthesized Au nanoparticles are localized within the hydrophilic (water) domains of the structure. At low Au nanoparticle content, the images reveal incomplete packing of spherical particles (i.e., voids) within these columns. The confinement and organization of the Au nanoparticles within the hydrophilic columns give rise to a large manifold of optical resonances in the near-IR region. The bulk composite conductivity, R{sub b}, was determined by ac electrochemical impedance spectroscopy (EIS) for samples prepared with increasing Au{sup 3+} content over a frequency range of 10 Hz to 1 MHz. A 100-fold increase was observed in the bulk conductivity at room temperature for composites prepared with the highest amount of Au{sup 3+} (1.58 {+-} 0.065 {micro}mol) versus the no Au composite, with the former reaching a value of 1.3 x 10{sup -4} S cm{sup -1} at 25 C. The temperature dependence of the conductivity recorded over this range was well-modeled by the Arrhenius equation. EIS studies on samples containing the highest Au nanoparticle content over a broader range of frequencies (2 x 10{sup -2} Hz to 5 x 10{sup 5} Hz) identified a low frequency component ascribed to electronic conduction. Electronic conduction due to aggregated Au nanoparticles was further confirmed by dc conductivity measurements. This work identifies a nanostructured composite that exhibits both ionic transport through the polymeric ionic liquid and electronic conduction from the organized encapsulated columns of Au nanoparticles.

Lee, S.; Cummins, M. D.; Willing, G. A.; Firestone, M. A.; Materials Science Division; Univ. of Louisville

2009-01-01T23:59:59.000Z

125

Oil-Miscible and Non-Corrosive Phosphonium Ionic Liquids as Candidate Lubricant Additives  

SciTech Connect (OSTI)

Ionic liquids (ILs) have been receiving considerable attention from the lubricants industry as potential friction and wear-reducing additives, but their solubility in oils is an issue. Unlike most ionic liquids that are insoluble in non-polar hydrocarbon oils, this study reports phosphonium-based ILs (PP-ILs) that are fully miscible with both mineral oil-based and synthetic lubricants. Both the cation and anion in quaternary structures, long alkyl chains, and capability of pairing the cation and the anion via a H-O bond are hypothesized to improve the compatibility between ions and neutral oil molecules. The measured viscosities of the oil-IL blends agree well with the Refutas equation that is for solutions containing multiple components. High thermal stability and non-corrosiveness were observed for the PP-ILs. Effective friction reduction and anti-wear functionality have been demonstrated in tribological tests when adding 5 wt% of a PP-IL into a base oil, suggesting potential applications for using the oil-miscible PP-ILs as lubricant additives.

Yu, Bo [ORNL; Bansal, Dinesh G [ORNL; Qu, Jun [ORNL; Sun, Xiaoqi [ORNL; Luo, Huimin [ORNL; Dai, Sheng [ORNL; Blau, Peter Julian [ORNL; Bunting, Bruce G [ORNL; Mordukhovich, Gregory [GM R& D and Planning, Warren, Michigan; Smolenski, Donald [GM R& D and Planning, Warren, Michigan

2012-01-01T23:59:59.000Z

126

Unusual mechanism for the short-range electron transfer within gold-alkanethiol-ionic-liquid films of subnanometer thickness  

SciTech Connect (OSTI)

Exploiting nanoscopically tunable composite gold-alkanethiol-ionic-liquid/ferrocene self-assembled systems with tunable electron transfer distance, we discovered in the case of thinner alkanethiol films a thermally activated electron transfer pattern totally controlled by the viscosity-related slow relaxation mode(s) of the ionic liquid acting as the reactant's fluctuating environment. This pattern manifested through the activation enthalpy and volume parameters that are identical to those for viscous flow was explained in terms of the extreme adiabatic mechanism with a vanishing Marcus barrier (via the exponential Franck-Condon-like term approaching unity).

Khoshtariya, Dimitri E. [Department of Physics and Institute for Biophysics and Bionanosciences, I. Javakhishvili Tbilisi State University, I. Chavchavadze Avenue 3, 0128 Tbilisi, Georgia (United States); Department of Chemistry and Pharmacy, University of Erlangen-Nuernberg, Egerlandstrasse 1, 91058 Erlangen (Germany); Institute of Molecular Biology and Biophysics and Institute of Inorganic Chemistry and Electrochemistry, Gotua 12, 0160 Tbilisi, Georgia (United States); Dolidze, Tina D. [Department of Chemistry and Pharmacy, University of Erlangen-Nuernberg, Egerlandstrasse 1, 91058 Erlangen (Germany); Institute of Molecular Biology and Biophysics and Institute of Inorganic Chemistry and Electrochemistry, Gotua 12, 0160 Tbilisi, Georgia (United States); Eldik, Rudi van [Department of Chemistry and Pharmacy, University of Erlangen-Nuernberg, Egerlandstrasse 1, 91058 Erlangen (Germany)

2009-12-15T23:59:59.000Z

127

Uranyl coordination environment in hydrophobic ionic liquids : an in situ investigation.  

SciTech Connect (OSTI)

Different inner-sphere coordination environments are observed for the uranyl nitrate complexes formed with octyl-phenyl-N,N-diisobutylcarbamoylmethylphosphine oxide and tributyl phosphate in dodecane and in the hydrophobic ionic liquids (ILs) [C{sub 4}mim][PF{sub 6}] and [C{sub 8}mim][N(SO{sub 2}CF{sub 3}){sub 2}]. Qualitative differences in the coordination environment of the extracted uranyl species are implied by changes in peak intensity patterns and locations for uranyl UV-visible spectral bands when the solvent is changed. EXAFS data for uranyl complexes in dodecane solutions is consistent with hexagonal bipyramidal coordination and the existence of UO{sub 2}(NO{sub 3}){sub 2}(CMPO){sub 2}. In contrast, the complexes formed when uranyl is transferred from aqueous nitric acid solutions into the ILs exhibit an average equatorial coordination number of approximately 4.5. Liquid/liquid extraction results for uranyl in both ILs indicate a net stoichiometry of UO{sub 2}(NO{sub 3})(CMPO){sup +}. The concentration of the IL cation in the aqueous phase increases in proportion to the amount of UO{sub 2}(NO{sub 3})(CMPO){sup +} in the IL phase, supporting a predominantly cation exchange mechanism for partitioning in the IL systems.

Visser, A. E.; Jensen, M. P.; Laszak, I.; Nash, K. L.; Choppin, G. R.; Roers, R. D.; Chemistry; Univ. of Alabama; Flordia State Univ.

2003-01-01T23:59:59.000Z

128

Click grafting of seaweed bioactive polysaccharides onto PVC surfaces using ionic liquid as green solvent and catalyst  

E-Print Network [OSTI]

Click grafting of seaweed bioactive polysaccharides onto PVC surfaces using ionic liquid as green Houssinière, BP 32229, 44322 Nantes, France A green and click approach of grafting polysaccharides onto PVC surfaces was developed. PVC isothiocyanate surfaces (PVC-NCS) were prepared by nucleofilic substitution

Boyer, Edmond

129

[Cu(I)(bpp)]BF4: the first extended coordination network prepared solvothermally in an ionic liquid solvent  

E-Print Network [OSTI]

, the two-dimensional net- work [Cu(bpp)]BF4 [bpp = 1,3-bis(4-pyridyl)propane], pro- duced via and 1,3-bis(4-pyridyl)propane (bpp) ligand. [bmim][BF4], as a room temperature ionic liquid, is air

Li, Jing

130

Improved dye-sensitized solar cells by composite ionic liquid electrolyte incorporating layered titanium phosphate  

SciTech Connect (OSTI)

We reported a composite electrolyte prepared by incorporating layered {alpha}-titanium phosphate ({alpha}-TiP) into a binary ionic liquid of 1-propyl-3-methylimidazolium iodide (PMII) and 1-ethyl-3-methylimidazolium tetrafluoroborate (EmimBF{sub 4}) (volume ratio, 13:7) electrolyte. The addition of {alpha}-TiP markedly improved the photovoltaic properties of dye-sensitized solar cells (DSSCs) compared to that without {alpha}-TiP. The enhancement was explained by improved diffusion of tri-iodide (I{sub 3}{sup -}) ions, suppressed electron recombination with I{sub 3}{sup -} in the electrolyte and increased lifetime of electrons in mesoscopic TiO{sub 2} film. (author)

Cheng, Ping; Lan, Tian; Wang, Wanjun; Wu, Haixia; Yang, Haijun; Guo, Shouwu [National Key Laboratory of Nano/Micro Fabrication Technology, Key Laboratory for Thin Film and Microfabrication of the Ministry of Education, Research Institute of Micro/Nano Science and Technology, Shanghai Jiao Tong University, Shanghai 200240 (China); Deng, Changsheng; Dai, Xiaming [Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing 100084 (China)

2010-05-15T23:59:59.000Z

131

Lubricants or lubricant additives composed of ionic liquids containing ammonium cations  

DOE Patents [OSTI]

A lubricant or lubricant additive is an ionic liquid alkylammonium salt. The alkylammonium salt has the structure R.sub.xNH.sub.(4-x).sup.+,[F.sub.3C(CF.sub.2).sub.yS(O).sub.2].sub.2N.sup- .- where x is 1 to 3, R is independently C.sub.1 to C.sub.12 straight chain alkyl, branched chain alkyl, cycloalkyl, alkyl substituted cycloalkyl, cycloalkyl substituted alkyl, or, optionally, when x is greater than 1, two R groups comprise a cyclic structure including the nitrogen atom and 4 to 12 carbon atoms, and y is independently 0 to 11. The lubricant is effective for the lubrication of many surfaces including aluminum and ceramics surfaces.

Qu, Jun (Knoxville, TN) [Knoxville, TN; Truhan, Jr.,; John J. (Cookeville, TN) [Cookeville, TN; Dai, Sheng (Knoxville, TN) [Knoxville, TN; Luo, Huimin (Knoxville, TN) [Knoxville, TN; Blau, Peter J. (Knoxville, TN) [Knoxville, TN

2010-07-13T23:59:59.000Z

132

Impact of Mixed Feedstocks and Feedstock Densification on Ionic Liquid Pretreatment Efficiency  

SciTech Connect (OSTI)

Background: Lignocellulosic biorefineries must be able to efficiently process the regional feedstocks that are available at cost-competitive prices year round. These feedstocks typically have low energy densities and vary significantly in composition. One potential solution to these issues is blending and/or densifying the feedstocks in order to create a uniform feedstock. Results/discussion: We have mixed four feedstocks - switchgrass, lodgepole pine, corn stover, and eucalyptus - in flour and pellet form and processed them using the ionic liquid 1-ethyl-3-methylimidazolium acetate. Sugar yields from both the mixed flour and pelletized feedstocks reach 90% within 24 hours of saccharification. Conclusions: Mixed feedstocks, in either flour or pellet form, are efficiently processed using this pretreatment process, and demonstrate that this approach has significant potential.

Jian Shi; Vicki S. Thompson; Neal A. Yancey; Vitalie Stavila; Blake A. Simmons; Seema Singh

2013-01-01T23:59:59.000Z

133

Free Radical Polymerization of Styrene and Methyl Methacrylate in Various Room Temperature Ionic Liquids  

SciTech Connect (OSTI)

Conventional free radical polymerization of styrene and methyl methacrylate was carried out in various room temperature ionic liquids (RTILs). The RTILs used in this research encompass a wide range of cations and anions. Typical cations include imidazolium, phosphonium, pyridinium, and pyrrolidinium; typical anions include amide, borate, chloride, imide, phosphate, and phosphinate. Reactions are faster and polymers obtained usually have higher molecular weights when compared to polymerizations carried out in volatile organic solvents under the same conditions. This shows that rapid rates of polymerization and high molecular weights are general features of conventional radical polymerizations in RTILs. Attempts to correlate the polarities and viscosities of the RTILs with the polymerization behavior fail to yield discernible trends.

Zhang, Hongwei [University of Tennessee, Knoxville (UTK); Hong, Kunlun [ORNL; Mays, Jimmy [ORNL

2005-01-01T23:59:59.000Z

134

Determining diffusion coefficients of ionic liquids by means of field cycling nuclear magnetic resonance relaxometry  

SciTech Connect (OSTI)

Field Cycling Nuclear Magnetic Resonance (FC NMR) relaxation studies are reported for three ionic liquids: 1-ethyl-3- methylimidazolium thiocyanate (EMIM-SCN, 220–258 K), 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM-BF{sub 4}, 243–318 K), and 1-butyl-3-methylimidazolium hexafluorophosphate (BMIM-PF{sub 6}, 258–323 K). The dispersion of {sup 1}H spin-lattice relaxation rate R{sub 1}(?) is measured in the frequency range of 10 kHz–20 MHz, and the studies are complemented by {sup 19}F spin-lattice relaxation measurements on BMIM-PF{sub 6} in the corresponding frequency range. From the {sup 1}H relaxation results self-diffusion coefficients for the cation in EMIM-SCN, BMIM-BF{sub 4}, and BMIM-PF{sub 6} are determined. This is done by performing an analysis considering all relevant intra- and intermolecular relaxation contributions to the {sup 1}H spin-lattice relaxation as well as by benefiting from the universal low-frequency dispersion law characteristic of Fickian diffusion which yields, at low frequencies, a linear dependence of R{sub 1} on square root of frequency. From the {sup 19}F relaxation both anion and cation diffusion coefficients are determined for BMIM-PF{sub 6}. The diffusion coefficients obtained from FC NMR relaxometry are in good agreement with results reported from pulsed- field-gradient NMR. This shows that NMR relaxometry can be considered as an alternative route of determining diffusion coefficients of both cations and anions in ionic liquids.

Kruk, D. [Faculty of Mathematics and Computer Science, University of Warmia and Mazury in Olsztyn, S?oneczna 54, PL-10710 Olsztyn (Poland); Universität Bayreuth, Experimentalphysik II, 95440 Bayreuth (Germany); Meier, R.; Rössler, E. A. [Universität Bayreuth, Experimentalphysik II, 95440 Bayreuth (Germany); Rachocki, A. [Institute of Molecular Physics, Polish Academy of Sciences, Smoluchowskiego 17, 60-179 Pozna? (Poland); Korpa?a, A. [Department of Biophysics, Jagiellonian University Medical College, ?azarza 16, 31-530 Kraków, Poland and Institute of Physics, Jagiellonian University, Reymonta 4, 30-059 Kraków (Poland); Singh, R. K. [Ionic Liquid and Solid State Ionics Laboratory, Department of Physics, Banaras Hindu University, Varanasi 221 005 (India)

2014-06-28T23:59:59.000Z

135

Methods for applying microchannels to separate methane using liquid absorbents, especially ionic liquid absorbents from a mixture comprising methane and nitrogen  

DOE Patents [OSTI]

Methods of using microchannel separation systems including absorbents to improve thermal efficiency and reduce parasitic power loss. Energy is typically added to desorb methane and then energy or heat is removed to absorb methane using a working solution. The working solution or absorbent may comprise an ionic liquid, or other fluids that demonstrate a difference in affinity between methane and nitrogen in a solution.

Tonkovich, Anna Lee Y. (Dublin, OH); Litt, Robert D. (Westerville, OH); Dongming, Qiu (Dublin, OH); Silva, Laura J. (Plain City, OH); Lamont, Micheal Jay (Plain City, OH); Fanelli, Maddalena (Plain City, OH); Simmons, Wayne W. (Plain city, OH); Perry, Steven (Galloway, OH)

2011-10-04T23:59:59.000Z

136

Radiation induced redox reactions and fragmentation of constituent ions in ionic liquids II. Imidazolium cations.  

SciTech Connect (OSTI)

In part 1 of this study, radiolytic degradation of constituent anions in ionic liquids (ILs) was examined. The present study continues the themes addressed in part 1 and examines the radiation chemistry of 1,3-dialkyl substituted imidazolium cations, which currently comprise the most practically important and versatile class of ionic liquid cations. For comparison, we also examined 1,3-dimethoxy- and 2-methyl-substituted imidazolium and 1-butyl-4-methylpyridinium cations. In addition to identification of radicals using electron paramagnetic resonance spectroscopy (EPR) and selective deuterium substitution, we analyzed stable radiolytic products using {sup 1}H and {sup 13}C nuclear magnetic resonance (NMR) and tandem electrospray ionization mass spectrometry (ESMS). Our EPR studies reveal rich chemistry initiated through 'ionization of the ions': oxidation and the formation of radical dications in the aliphatic arms of the parent cations (leading to deprotonation and the formation of alkyl radicals in these arms) and reduction of the parent cation, yielding 2-imidazolyl radicals. The subsequent reactions of these radicals depend on the nature of the IL. If the cation is 2-substituted, the resulting 2-imidazolyl radical is relatively stable. If there is no substitution at C(2), the radical then either is protonated or reacts with the parent cation forming a C(2)-C(2) {sigma}{sigma}*-bound dimer radical cation. In addition to these reactions, when methoxy or C{sub {alpha}}-substituted alkyl groups occupy the N(1,3) positions, their elimination is observed. The elimination of methyl groups from N(1,3) was not observed. Product analyses of imidazolium liquids irradiated in the very-high-dose regime (6.7 MGy) reveal several detrimental processes, including volatilization, acidification, and oligomerization. The latter yields a polymer with m/z of 650 {+-} 300 whose radiolytic yield increases with dose (0.23 monomer units per 100 eV for 1-methyl-3-butylimidazolium trifluorosulfonate). Gradual generation of this polymer accounts for the steady increase in the viscosity of the ILs upon irradiation. Previous studies at lower dose have missed this species due to its wide mass distribution (stretching out to m/z 1600) and broad NMR lines, which make it harder to detect at lower concentrations. Among other observed changes is the formation of water immiscible fractions in hydrophilic ILs and water miscible fractions in hydrophobic ILs. The latter is due to anion fragmentation. The import of these observations for use of ILs as extraction solvents in nuclear cycle separations is discussed.

Shkrob, I. A.; Marin, T. W.; Chemerisov, S. D.; Hatcher, J.; Wishart, J. (Chemical Sciences and Engineering Division); (BNL)

2011-04-14T23:59:59.000Z

137

Bis(fluoromalonato)borate (BFMB) Anion Based Ionic Liquid As an Additive for Lithium-Ion Battery Electrolytes  

SciTech Connect (OSTI)

Propylene carbonate (PC) is a good solvent for lithium ion battery applications due to its low melting point and high dielectric constant. However, PC is easily intercalated into graphite causing it to exfoliate, killing its electrochemical performance. Here we report on the synthesis of a new ionic liquid electrolyte based on partially fluorinated borate anion, 1-butyl-1,2-dimethylimidazolium bis(fluoromalonato)borate (BDMIm.BFMB), which can be used as an additive in 1 M LiPF6/PC electrolyte to suppress graphite exfoliation and improve cycling performance. In addition, both PC and BDMIm.BFMB can be used synergistically as additive to 1.0M LiPF6/methyl isopropyl sulfone (MIPS) to dramatically improve its cycling performance. It is also found that the chemistry nature of the ionic liquids has dramatic effect on their role as additive in PC based electrolyte.

Sun, Xiao-Guang [ORNL] [ORNL; Liao, Chen [ORNL] [ORNL; Baggetto, Loic [ORNL] [ORNL; Guo, Bingkun [ORNL] [ORNL; Unocic, Raymond R [ORNL] [ORNL; Veith, Gabriel M [ORNL] [ORNL; Dai, Sheng [ORNL] [ORNL

2014-01-01T23:59:59.000Z

138

An XAFS Study of Nickel Chloride in the Ionic Liquid 1-ethyl-3-methyl Imidazolium Chloride/ Aluminum Chloride  

SciTech Connect (OSTI)

The electrodeposition of metals from aqueous solutions has a successful history for many metals. However, some metals cannot be deposited from aqueous solutions because their potentials fall outside of the window of stability for water. Using ionic liquids for the electrodeposition of metals can avoid some of these difficulties because they have a larger region of stability than water. The electrochemical window can be tailored to fit a particular application by choosing appropriate anions and cations to form the melt. There is also the possibility to deposit pure metals without the oxides and hydrides that can form in aqueous solutions. The study of the structure of metal salts in ionic liquids is an important step towards achieving these goals.

Roeper, D.; Cheek, G; Pandya, K; O'Gragy, W

2008-01-01T23:59:59.000Z

139

Vehicle Technologies Office Merit Review 2014: Ionic Liquids as Anti-Wear Additives for Next-Generation Low-Viscosity Fuel-Efficient Engine Lubricants  

Broader source: Energy.gov [DOE]

Presentation given by Oak Ridge National Laboratory at 2014 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Office Annual Merit Review and Peer Evaluation Meeting about ionic liquids...

140

Hormetic effect of ionic liquid 1-ethyl-3-methylimidazolium acetate on bacteria  

DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

The biological effect of ionic liquids (ILs) is one of the highly debated topics as they are being contemplated for various industrial applications. 1-ethyl-2-methylimidazolium acetate ([EMIM][Ac]) showed remarkable hormesis on anaerobic Clostridium sp. and aerobic Psueudomonas putida. Bacterial growth was stimulated at up to 2.5 g L-1 and inhibited at > 2.5 g L-1 of ([EMIM][Ac]). The growth of Clostridium sp. and P. putida were higher by 0.4 and 4-fold respectively, in the presense of 0.5 g L-1 of ([EMIM][Ac]). Assessment of the effect of [EMIM][Ac] under different growth conditions showed that the hormesis of [EMIM][Ac] was mediated via regulation of medium pH. Hormetic effect of [EMIM][Ac] was evident only in medium with poor buffering capacity and in the presence of a fermentable substrate as the carbon source. The hormetic effect of [EMIM][Ac] on bacterial growth is most likely associated with the buffering capacity of acetate anion. These observations have implications in ILs toxicity studies and ecological risk assessment.

Nancharaiah, Y. V. [Bhabha Atomic Research Center, Kalpakkam (India). Biofouling and Biofilm Processes Sect.; Francis, A. J. [Brookhaven National Laboratory (BNL), Upton, NY (United States). Environmental Sciences Dept.; POSTECH, Pohang (Korea, Rep. of). Div. of Advanced Nuclear Engineering

2015-06-01T23:59:59.000Z

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141

Ionic Liquid-Enhanced Solid State Electrolyte Interface (SEI) for Lithium Sulfur Batteries  

SciTech Connect (OSTI)

Li-S battery is a complicated system with many challenges existing before its final market penetration. While most of the reported work for Li-S batteries is focused on the cathode design, we demonstrate in this work that the anode consumption accelerated by corrosive polysulfide solution also critically determines the Li-S cell performance. To validate this hypothesis, ionic liquid (IL) N-methyl-N-butylpyrrolidinium bis(trifluoromethylsulfonyl)imide (Py14TFSI) has been employed to modify the properties of SEI layer formed on Li metal surface in Li-S batteries. It is found that the IL-enhanced passivation film on the lithium anode surface exhibits much different morphology and chemical compositions, effectively protecting lithium metal from continuous attack by soluble polysulfides. Therefore, both cell impedance and the irreversible consumption of polysulfides on lithium metal are reduced. As a result, the Coulombic efficiency and the cycling stability of Li-S batteries have been greatly improved. After 120 cycles, Li-S battery cycled in the electrolyte containing IL demonstrates a high capacity retention of 94.3% at 0.1 C rate. These results unveil another important failure mechanism for Li-S batteries and shin the light on the new approaches to improve Li-S battery performances.

Zheng, Jianming; Gu, Meng; Chen, Honghao; Meduri, Praveen; Engelhard, Mark H.; Zhang, Jiguang; Liu, Jun; Xiao, Jie

2013-05-16T23:59:59.000Z

142

Tribological characteristics of aluminum alloys against steel lubricated by ammonium and imidazolium ionic liquids  

SciTech Connect (OSTI)

Sliding friction and wear characteristics of aluminum alloys against AISI 52100 steel lubricated by ionic liquids (ILs) were investigated at both room and elevated temperatures. The tested aluminum alloys include a commercially pure aluminum Al 1100, a wrought alloy Al 6061-T6511, and a cast alloy Al 319-T6. The lubricating performance of two ILs with the same anion, one ammonium-based [C8H17]3NH.Tf2N and one imidazolium-based C10mim.Tf2N, were compared each other and benchmarked against that of a conventional fully-formulated engine oil. Significant friction (up to 35%) and wear (up to 55%) reductions were achieved by the ammonium IL when lubricating the three aluminum alloys compared to the engine oil. The imidazolium IL performed better than the oil but not as well as the ammonium IL for Al 1100 and 319 alloys. However, accelerated wear was unexpectedly observed for Al 6061 alloy when lubricated by C10mim.Tf2N. Surface chemical analyses implied complex tribochemical reactions between the aluminum surfaces and ILs during the wear testing, which has been demonstrated either beneficial by forming a protective boundary film or detrimental by causing severe tribo-corrosion. The effects of the IL cation structure, aluminum alloy composition, and tribo-testing condition on the friction and wear results have been discussed.

Qu, Jun [ORNL; Blau, Peter Julian [ORNL; Dai, Sheng [ORNL; Luo, Huimin [ORNL; Meyer III, Harry M [ORNL; Truhan, John J. [Caterpillar Inc.

2009-01-01T23:59:59.000Z

143

Effect of ionic liquid treatment on the structures of lignins in solutions  

SciTech Connect (OSTI)

The solution structures of three types of isolated lignin - organosolv (OS), Kraft (K), and low sulfonate (LS) - before and after treatment with 1-ethyl-3-methylimidazolium acetate were studied using small-angle neutron scattering (SANS) and dynamic light scattering (DLS) over a concentration range of 0.3-2.4 wt %. The results indicate that each of these lignins is comprised of aggregates of well-defined basal subunits, the shapes and sizes of which, in D{sub 2}O and DMSO-d{sub 6}, are revealed using these techniques. LS lignin contains a substantial amount of nanometer-scale individual subunits. In aqueous solution these subunits have a well-defined elongated shape described well by ellipsoidal and cylindrical models. At low concentration the subunits are highly expanded in alkaline solution, and the effect is screened with increasing concentration. OS lignin dissolved in DMSO was found to consist of a narrow distribution of aggregates with average radius 200 {+-} 30 nm. K lignin in DMSO consists of aggregates with a very broad size distribution. After ionic liquid (IL) treatment, LS lignin subunits in alkaline solution maintained the elongated shape but were reduced in size. IL treatment of OS and K lignins led to the release of nanometer-scale subunits with well-defined size and shape.

Cheng, Gang [Joint Bioenergy Institute; Kent, Michael S [ORNL; He, Lilin [ORNL; Varanasi, Patanjali [Joint Bioenergy Institute; Dibble, Dean [Joint Bioenergy Institute; Melnichenko, Yuri B [ORNL; Simmons, Blake [Sandia National Laboratories (SNL); Singh, Seema [Joint Bioenergy Institute

2012-01-01T23:59:59.000Z

144

Physical insight into switchgrass dissolution in the ionic liquid 1-ethyl-3-methylimidazolium acetate  

SciTech Connect (OSTI)

Small-angle neutron scattering was used to characterize solutions of switchgrass and the constituent biopolymers cellulose, hemicellulose, and lignin, as well as a physical mixture of them mimicking the composition of switchgrass, dissolved in the ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate. The results demonstrate that the IL dissolves the cellulose fibrils of switchgrass, although a supramolecular biopolymer network remains that is not present in solutions of the individual biopolymers and that does not self-assemble in a solution containing the physical mixture of the individual biopolymers. The persistence of a network-like structure indicates that dissolving switchgrass in the IL does not disrupt all of the physical entanglements and covalent linkages between the biopolymers created during plant growth. Reconstitution of the IL-dissolved switchgrass yields carbohydrate-rich material containing cellulose with a low degree of crystallinity, as determined by powder X-ray diffraction, which impacts potential down-stream uses of the biopolymers produced by the process. The data suggests that the use of chemical additives which would break bonds that exist between the lignin and hemicellulose might improve the purity of the resulting product, but may not be able to disrupt the highly physically-entangled biopolymer network sufficiently to facilitate their separation.

Wang, Hui [University of Alabama, Tuscaloosa] [University of Alabama, Tuscaloosa; Gurau, Gabriela [University of Alabama, Tuscaloosa] [University of Alabama, Tuscaloosa; Pingali, Sai Venkatesh [ORNL] [ORNL; O'Neil, Hugh [ORNL] [ORNL; Evans, Barbara R [ORNL] [ORNL; Urban, Volker S [ORNL] [ORNL; Heller, William T [ORNL] [ORNL; Rogers, Robin D [University of Alabama, Tuscaloosa] [University of Alabama, Tuscaloosa

2014-01-01T23:59:59.000Z

145

Lithium-sulfur batteries based on nitrogen-doped carbon and ionic liquid electrolyte  

SciTech Connect (OSTI)

Nitrogen-doped mesoporous carbon (NC) and sulfur were used to prepare an NC/S composite cathode, which was evaluated in an ionic liquid electrolyte of 0.5 M lithium bis(trifluoromethane sulfonyl)imide (LiTFSI) in methylpropylpyrrolidinium bis(trifluoromethane sulfonyl)imide (MPPY.TFSI) by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and cycle testing. To facilitate the comparison, a C/S composite based on activated carbon (AC) without nitrogen doping was also fabricated under the same conditions as those for the NC/S composite. Compared with the AC/S composite, the NC/S composite showed enhanced activity toward sulfur reduction, as evidenced by the early onset sulfur reduction potential, higher redox current density in the CV test, and faster charge transfer kinetics as indicated by EIS measurement. At room temperature under a current density of 84 mA g-1 (C/20), the battery based on the NC/S composite exhibited higher discharge potential and an initial capacity of 1420 mAh g-1 whereas that based on the AC/S composite showed lower discharge potential and an initial capacity of 1120 mAh g-1. Both batteries showed similar capacity fading with cycling due to the intrinsic polysulfide solubility and the polysulfide shuttle mechanism; the capacity fading can be improved by further modification of the cathode.

Sun, Xiao-Guang [ORNL; Wang, Xiqing [ORNL; Mayes, Richard T [ORNL; Dai, Sheng [ORNL

2012-01-01T23:59:59.000Z

146

Electrochemical Polishing Applications and EIS of a Vitamin B{sub 4}-Based Ionic Liquid  

SciTech Connect (OSTI)

Modern particle accelerators require minimal interior surface roughness for Niobium superconducting radio frequency (SRF) cavities. Polishing of the Nb is currently achieved via electrochemical polishing with concentrated mixtures of sulfuric and hydrofluoric acids. This acid-based approach is effective at reducing the surface roughness to acceptable levels for SRF use, but due to acid-related hazards and extra costs (including safe disposal of used polishing solutions), an acid-free method would be preferable. This study focuses on an alternative electrochemical polishing method for Nb, using a novel ionic liquid solution containing choline chloride, also known as Vitamin B{sub 4} (VB{sub 4}). Potentiostatic electrochemical impedance spectroscopy (EIS) was also performed on the VB4-based system. Nb polished using the VB4-based method was found to have a final surface roughness comparable to that achieved via the acid-based method, as assessed by atomic force microscopy (AFM). These findings indicate that acid-free VB{sub 4}-based electrochemical polishing of Nb represents a promising replacement for acid-based methods of SRF cavity preparation.

Wixtrom, Alex I. [Christopher Newport University, Newport News, VA (United States); Buhler, Jessica E. [Christopher Newport University, Newport News, VA (United States); Reece, Charles E. [Thomas Jefferson National Accelerator Facility, Newport News, VA (United States); Abdel-Fattah, Tarek M. [Christopher Newport University, Newport News, VA (United States)

2013-01-01T23:59:59.000Z

147

Lithium Ion Transport Mechanism in Ternary Polymer Electrolyte-Ionic Liquid Mixtures - A Molecular Dynamics Simulation Study  

E-Print Network [OSTI]

The lithium transport mechanism in ternary polymer electrolytes, consisting of PEO/LiTFSI and various fractions of the ionic liquid N-methyl-N-propylpyrrolidinium bis(trifluoromethane)sulfonimide, are investigated by means of MD simulations. This is motivated by recent experimental findings [Passerini et al., Electrochim. Acta 2012, 86, 330-338], which demonstrated that these materials display an enhanced lithium mobility relative to their binary counterpart PEO/LiTFSI. In order to grasp the underlying microscopic scenario giving rise to these observations, we employ an analytical, Rouse-based cation transport model [Maitra at al., PRL 2007, 98, 227802], which has originally been devised for conventional polymer electrolytes. This model describes the cation transport via three different mechanisms, each characterized by an individual time scale. It turns out that also in the ternary electrolytes essentially all lithium ions are coordinated by PEO chains, thus ruling out a transport mechanism enhanced by the presence of ionic-liquid molecules. Rather, the plasticizing effect of the ionic liquid contributes to the increased lithium mobility by enhancing the dynamics of the PEO chains and consequently also the motion of the attached ions. Additional focus is laid on the prediction of lithium diffusion coefficients from the simulation data for various chain lengths and the comparison with experimental data, thus demonstrating the broad applicability of our approach.

Diddo Diddens; Andreas Heuer

2013-02-20T23:59:59.000Z

148

Ionic Liquid and Supercritical Fluid Hyphenated Techniques for Dissolution and Separation of Lanthanides, Actinides, and Fission Products  

SciTech Connect (OSTI)

This project is investigating techniques involving ionic liquids (IL) and supercritical (SC) fluids for dissolution and separation of lanthanides, actinides, and fission products. The research project consists of the following tasks: Study direct dissolution of lanthanide oxides, uranium dioxide and other actinide oxides in [bmin][Tf{sub 2}N] with TBP(HNO{sub 3}){sub 1.8}(H{sub 2}O){sub 0.6} and similar types of Lewis acid-Lewis base complexing agents; Measure distributions of dissolved metal species between the IL and the sc-CO{sub 2} phases under various temperature and pressure conditions; Investigate the chemistry of the dissolved metal species in both IL and sc-CO{sub 2} phases using spectroscopic and chemical methods; Evaluate potential applications of the new extraction techniques for nuclear waste management and for other projects. Supercritical carbon dioxide (sc-CO{sub 2}) and ionic liquids are considered green solvents for chemical reactions and separations. Above the critical point, CO{sub 2} has both gas- and liquid-like properties, making it capable of penetrating small pores of solids and dissolving organic compounds in the solid matrix. One application of sc-CO{sub 2} extraction technology is nuclear waste management. Ionic liquids are low-melting salts composed of an organic cation and an anion of various forms, with unique properties making them attractive replacements for the volatile organic solvents traditionally used in liquid-liquid extraction processes. One type of room temperature ionic liquid (RTIL) based on the 1-alkyl-3-methylimidazolium cation [bmin] with bis(trifluoromethylsulfonyl)imide anion [Tf{sub 2}N] is of particular interest for extraction of metal ions due to its water stability, relative low viscosity, high conductivity, and good electrochemical and thermal stability. Recent studies indicate that a coupled IL sc-CO{sub 2} extraction system can effectively transfer trivalent lanthanide and uranyl ions from nitric acid solutions. Advantages of this technique include operation at ambient temperature and pressure, selective extraction due to tunable sc-CO{sub 2} solvation strength, no IL loss during back-extraction, and no organic solvent introduced into the IL phase.

Wai, Chien M. [Univ. of Idaho, Moscow, ID (United States); Bruce Mincher

2012-12-01T23:59:59.000Z

149

THE POTENTIAL OF NANOPARTICLE ENHANCED IONIC LIQUIDS (NEILS) AS ADVANCED HEAT TRANSFER FLUIDS  

SciTech Connect (OSTI)

Interest in capturing the energy of the sun is rising as demands for renewable energy sources increase. One area of developing research is the use of concentrating solar power (CSP), where the solar energy is concentrated by using mirrors to direct the sunlight towards a collector filled with a heat transfer fluid (HTF). The HTF transfers the collected energy into pressurized steam, which is used to generate energy. The greater the energy collected by the HTF, the more efficent the electrical energy production is, thus the overall efficiency is controlled by the thermal fluid. Commercial HTFs such as Therminol{reg_sign} (VP-1), which is a blend of biphenyl and diphenyl oxide, have a significant vapor pressure, especially at elevated temperatures. In order for these volatile compounds to be used in CSP systems, the system either has to be engineered to prevent the phase change (i.e., volatilization and condensation) through pressurization of the system, or operate across the phase change. Over thirty years ago, a class of low-melting organic compounds were developed with negligible vapor pressure. These compounds are referred to as ionic liquids (ILs), which are organic-based compounds with discrete charges that cause a significant decrease in their vapor pressure. As a class, ILs are molten salts with a melting point below 100 C and can have a liquidus range approaching 400 C, and in several cases freezing points being below 0 C. Due to the lack of an appreciable vapor pressure, volatilization of an IL is not possible at atmospheric pressure, which would lead to a simplification of the design if used as a thermal fluid and for energy storage materials. Though the lack of a vapor pressure does not make the use of ILs a better HTF, the lack of a vapor pressure is a compliment to their higher heat capacity, higher volummetric density, and thus higher volumetric heat capacity. These favorable physical properties give ILs a pontential advantage over the current commerically used thermal fluids. Also within the past decade nanofluids have gained attention for thermal conductivity enhancment of fluids, but little analysis has been completed on the heat capacity effects of the nanoparticle addition. The idea of ILs or nanofluids as a HTF is not new, as there are several references that have proposed the idea. However, the use of ionic liquid nanofluids containing nanomaterials other than carbon nanotubes has never before been studied. Here, for the first time, nano-particle enhanced ILs (NEILs) have been shown to increase the heat capacity of the IL with no adverse side effects to the ILs thermal stability and, only at high nanoparticle loading, are the IL physical properties affected. An increase of volumetric heat capacity translates into a better heat transfer fluid as more energy is stored per volumetric unit in the solar concentrating section, thus more efficency in increased steam pressure. Results show that the properties of the NEIL are highly dependant on the suspended nanomaterial and careful materials selection is required to fully optimize the nanofluid properties.

Fox, E.; Bridges, N.; Visser, A.

2011-09-14T23:59:59.000Z

150

The importance of ion size and electrode curvature on electrical double layers in ionic liquids  

SciTech Connect (OSTI)

Room-temperature ionic liquids (ILs) are an emerging class of electrolytes for supercapacitors. We investigate the effects of ion size and electrode curvature on the electrical double layers (EDLs) in two ILs 1-butyl-3-methylimidazolium chloride [BMIM][Cl] and 1-butyl-3-methylimidazolium hexafluorophosphate [BMIM][PF{sub 6}], using a combination of molecular dynamics (MD) and quantum density functional theory (DFT) simulations. The sizes of the counter-ion and co-ion affect the ion distribution and orientational structure of EDLs. The EDL capacitances near both planar and cylindrical electrodes were found to follow the order: [BMIM][Cl] (near the positive electrode) > [BMIM][PF{sub 6}] (near the positive electrode) ? [BMIM][Cl] (near the negative electrode) ? [BMIM][PF{sub 6}] (near the negative electrode). The EDL capacitance was also found to increase as the electrode curvature increases. These capacitance data can be fit to the Helmholtz model and the recently proposed exohedral electrical double-cylinder capacitor (xEDCC) model when the EDL thickness is properly parameterized, even though key features of the EDLs in ILs are not accounted for in these models. To remedy the shortcomings of existing models, we propose a “Multiple Ion Layers with Overscreening” (MILO) model for the EDLs in ILs that takes into account two critical features of such EDLs, i.e., alternating layering of counter-ions and co-ions and charge overscreening. The capacitance computed from the MILO model agrees well with the MD prediction. Although some input parameters of the MILO model must be obtained from MD simulations, the MILO model may provide a new framework for understanding many important aspects of EDLs in ILs (e.g., the variation of EDL capacitance with the electrode potential) that are difficult to interpret using classical EDL models and experiments.

Feng, G.; Qiao, R.; Huang, J; Dai, S.; Sumpter, B. G.; Meunier, V.

2011-01-01T23:59:59.000Z

151

The Importance of Ion Size and Electrode Curvature on Electrical Double Layers in Ionic Liquids  

SciTech Connect (OSTI)

Room-temperature ionic liquids (ILs) are an emerging class of electrolytes for supercapacitors. We investigate the effects of ion size and electrode curvature on the electrical double layers (EDLs) in two ILs 1-butyl-3-methylimidazolium chloride [BMIM][Cl] and 1-butyl-3-methylimidazolium hexafluorophosphate [BMIM][PF(6)], using a combination of molecular dynamics (MD) and quantum density functional theory (DFT) simulations. The sizes of the counter-ion and co-ion affect the ion distribution and orientational structure of EDLs. The EDL capacitances near both planar and cylindrical electrodes were found to follow the order: [BMIM][Cl] (near the positive electrode) > [BMIM][PF(6)] (near the positive electrode) {approx} [BMIM][Cl] (near the negative electrode) {approx} [BMIM][PF(6)] (near the negative electrode). The EDL capacitance was also found to increase as the electrode curvature increases. These capacitance data can be fit to the Helmholtz model and the recently proposed exohedral electrical double-cylinder capacitor (xEDCC) model when the EDL thickness is properly parameterized, even though key features of the EDLs in ILs are not accounted for in these models. To remedy the shortcomings of existing models, we propose a 'Multiple Ion Layers with Overscreening' (MILO) model for the EDLs in ILs that takes into account two critical features of such EDLs, i.e., alternating layering of counter-ions and co-ions and charge overscreening. The capacitance computed from the MILO model agrees well with the MD prediction. Although some input parameters of the MILO model must be obtained from MD simulations, the MILO model may provide a new framework for understanding many important aspects of EDLs in ILs (e.g., the variation of EDL capacitance with the electrode potential) that are difficult to interpret using classical EDL models and experiments.

Feng, Guang [Clemson University; Qiao, Rui [ORNL; Huang, Jingsong [ORNL; Dai, Sheng [ORNL; Sumpter, Bobby G [ORNL; Meunier, Vincent [ORNL

2010-01-01T23:59:59.000Z

152

Identification of a haloalkaliphilic and thermostable cellulase with improved ionic liquid tolerance  

SciTech Connect (OSTI)

Some ionic liquids (ILs) have been shown to be very effective solvents for biomass pretreatment. It is known that some ILs can have a strong inhibitory effect on fungal cellulases, making the digestion of cellulose inefficient in the presence of ILs. The identification of IL-tolerant enzymes that could be produced as a cellulase cocktail would reduce the costs and water use requirements of the IL pretreatment process. Due to their adaptation to high salinity environments, halophilic enzymes are hypothesized to be good candidates for screening and identifying IL-resistant cellulases. Using a genome-based approach, we have identified and characterized a halophilic cellulase (Hu-CBH1) from the halophilic archaeon, Halorhabdus utahensis. Hu-CBH1 is present in a gene cluster containing multiple putative cellulolytic enzymes. Sequence and theoretical structure analysis indicate that Hu-CBH1 is highly enriched with negatively charged acidic amino acids on the surface, which may form a solvation shell that may stabilize the enzyme, through interaction with salt ions and/or water molecules. Hu-CBH1 is a heat tolerant haloalkaliphilic cellulase and is active in salt concentrations up to 5 M NaCl. In high salt buffer, Hu-CBH1 can tolerate alkali (pH 11.5) conditions and, more importantly, is tolerant to high levels (20percent w/w) of ILs, including 1-allyl-3-methylimidazolium chloride ([Amim]Cl). Interestingly, the tolerances to heat, alkali and ILs are found to be salt-dependent, suggesting that the enzyme is stabilized by the presence of salt. Our results indicate that halophilic enzymes are good candidates for the screening of IL-tolerant cellulolytic enzymes.

Zhang, Tao; Datta, Supratim; Eichler, Jerry; Ivanova, Natalia; Axen, Seth D.; Kerfeld, Cheryl A.; Chen, Feng; Kyrpides, Nikos; Hugenholtz, Philip; Cheng, Jan-Fang; Sale, Kenneth L.; Simmons, Blake; Rubin, Eddy

2011-02-17T23:59:59.000Z

153

Generation of gas-phase zirconium fluoroanions by electrospray of an ionic liquid  

SciTech Connect (OSTI)

RATIONALE: When measuring extremely wide isotope ratios (= 1 x 109) accelerator mass spectrometry (AMS) is the instrument of choice, however it requires an anion for injection into the tandem accelerator. Since many elements do not have positive electronegativities they do not form stable negative atomic ions, and hence are not compatible for isotope ratio measurement using AMS. Thus new approaches for forming anions are sought; fluoroanions are particularly attractive because fluorine is monoisotopic, and thus will not have overlapping isobars with the isotope of interest. METHODS: An approach is described for making zirconium fluoroanions using the fluorinating ionic liquid (IL) 1-ethyl-3-methylimidazolium fluorohydrogenate, which was used to generate abundant [ZrF5-] using electrospray ionization. The IL was dissolved in acetonitrile, combined with a dilute solution of either Zr4+ or ZrO2+, and then electrosprayed. Mass analysis and collision induced dissociation were conducted using a time-of-flight mass spectrometer. Cluster structures were predicted using density functional theory calculations. RESULTS: The fluorohydrogenate IL solutions generated abundant [ZrF5-] starting from solutions of both Zr4+ and ZrO2+. The mass spectra also contained IL-bearing cluster ions, whose compositions indicated the presence of [ZrF6]2- in solution, a conclusion supported by the structural calculations. Rinsing out the zirconium-IL solution with acetonitrile decreased the IL clusters, but enhanced [ZrF5]-, which was sorbed by the polymeric electrospray supply capillary, and then released upon rinsing. This reduced the ion background in the mass spectrum. CONCLUSIONS: The fluorohydrogenate-IL solutions are a facile way to form zirconium fluoroanions in the gas phase using electrospray. The approach has potential as a source of fluoroanions for injection into an AMS, which would enable high-sensitivity measurement of minor zirconium isotopes, and benefits from the absence of overlapping isobars caused by the charge carrier (i.e., the monoisotopic fluorine atoms).

Gary S. Groenewold; James E. Delmore; Michael T. Benson; Tetsuya Tsuda; Rika Hagiwara

2014-06-01T23:59:59.000Z

154

E-Print Network 3.0 - aqueous ionic liquids Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

jcis Summary: experiments: ethanol, ultra- pure water, and four aqueous solutions of CaCl2 of different ionic strength... the correlations given by Weissenborn et al. 16, who...

155

EXPERIMENTAL INVESTIGATION OF NATURAL CONVECTION HEAT TRANSFER OF IONIC LIQUID IN A RECTANGULAR ENCLOSURE HEATED FROM BELOW  

SciTech Connect (OSTI)

This paper presents an experimental study of natural convection heat transfer for an Ionic Liquid. The experiments were performed for 1-butyl-2, 3-dimethylimidazolium bis(trifluoromethylsulfonyl)imide, ([C{sub 4}mmim][NTf{sub 2}]) at a Raleigh number range of 1.26 x 10{sup 7} to 8.3 x 10{sup 7}. In addition to determining the convective heat transfer coefficients, this study also included experimental determination of thermophysical properties of [C{sub 4}mmim][NTf{sub 2}] such as, density, viscosity, heat capacity, and thermal conductivity. The results show that the density of [C{sub 4}mmim][NTf{sub 2}] varies from 1.437-1.396 g/cm{sup 3} within the temperature range of 10-50 C, the thermal conductivity varies from 0.105-0.116 W/m.K between a temperature of 10 to 60 C, the heat capacity varies from 1.015 J/g.K - 1.760 J/g.K within temperature range of 25-340 C and the viscosity varies from 18cp-243cp within temperature range 10-75 C. The results for density, thermal conductivity, heat capacity, and viscosity were in close agreement with the values in the literature. Measured dimensionless Nusselt number was observed to be higher for the ionic liquid than that of DI water. This is expected as Nusselt number is the ratio of heat transfer by convection to conduction and the ionic liquid has lower thermal conductivity (approximately 18%) than DI water.

Fox, E.; Visser, A.; Bridges, N.

2011-07-18T23:59:59.000Z

156

E-Print Network 3.0 - ammonium-based ionic liquids Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Energy 65 Use of polymerionic liquid plasticizers as gel electrolytes in electrochromic devices Summary: Use of polymerionic liquid plasticizers as gel electrolytes in...

157

E-Print Network 3.0 - alkylammonium ionic liquids Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Energy 99 Use of polymerionic liquid plasticizers as gel electrolytes in electrochromic devices Summary: Use of polymerionic liquid plasticizers as gel electrolytes in...

158

E-Print Network 3.0 - alkylimidazolium ionic liquids Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Energy 73 Use of polymerionic liquid plasticizers as gel electrolytes in electrochromic devices Summary: Use of polymerionic liquid plasticizers as gel electrolytes in...

159

Conductance modulation in topological insulator Bi{sub 2}Se{sub 3} thin films with ionic liquid gating  

SciTech Connect (OSTI)

A Bi{sub 2}Se{sub 3} topological insulator field effect transistor is investigated by using ionic liquid as an electric double layer gating material, leading to a conductance modulation of 365% at room temperature. We discuss the role of charged impurities on the transport properties. The conductance modulation with gate bias is due to a change in the carrier concentration, whereas the temperature dependent conductance change is originated from a change in mobility. Large conductance modulation at room temperature along with the transparent optical properties makes topological insulators as an interesting (opto)electronic material.

Son, Jaesung; Banerjee, Karan; Yang, Hyunsoo, E-mail: eleyang@nus.edu.sg [Department of Electrical and Computer Engineering, National University of Singapore, 4 Engineering Drive 3, Singapore 117576 (Singapore)] [Department of Electrical and Computer Engineering, National University of Singapore, 4 Engineering Drive 3, Singapore 117576 (Singapore); Brahlek, Matthew; Koirala, Nikesh; Oh, Seongshik [Department of Physics and Astronomy, Rutgers, The State University of New Jersey, 136 Frelinghuysen Road, Piscataway, New Jersey 08854 (United States)] [Department of Physics and Astronomy, Rutgers, The State University of New Jersey, 136 Frelinghuysen Road, Piscataway, New Jersey 08854 (United States); Lee, Seoung-Ki [School of Advanced Materials Science and Engineering, Sungkyunkwan University, Suwon 440-746 (Korea, Republic of) [School of Advanced Materials Science and Engineering, Sungkyunkwan University, Suwon 440-746 (Korea, Republic of); School of Electrical and Electronic Engineering, Yonsei University, Seoul 120-749 (Korea, Republic of); Ahn, Jong-Hyun [School of Electrical and Electronic Engineering, Yonsei University, Seoul 120-749 (Korea, Republic of)] [School of Electrical and Electronic Engineering, Yonsei University, Seoul 120-749 (Korea, Republic of)

2013-11-18T23:59:59.000Z

160

Effects of liquid pore water on acoustic wave propagation in snow as a Biot-type porous material  

E-Print Network [OSTI]

A method to estimate phase velocity and attenuation of acoustic waves in the presence of liquid water in a snowpack is presented. The method is based on Biot's theory of wave propagation in porous materials. Empirical relations and a priori information is used to characterize snow as a porous material as a function of porosity. Plane wave theory and an equivalent pore fluid are used to solve Biot's differential equations and to asses the impact of the air and water in the pore space. The liquid water in the pore space of a snow pack reduces the velocity of the first compressional wave by roughly 300 m/s for every 0.1 increase in liquid water saturation. Also the attenuation of the compressional waves is increased with increasing liquid water content. Two end member models for compaction are evaluated to asses the importance of an independent density measurement for an estimate of liquid pore water saturation in snow with acoustic waves. The two end members correspond to no compaction at all and to a melting s...

Sidler, Rolf

2015-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
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161

Energy applications of ionic liquids Douglas R. MacFarlane,*a  

E-Print Network [OSTI]

volatility coupled with high electrochemical and thermal stability, as well as ionic conductivity, create of phase-change thermal energy storage materials having melting points tuned to the application important candidates for a number of energy related applications. Cation­anion combinations that exhibit low

Angell, C. Austen

162

Inexpensive, Nonfluorinated Anions for Lithium Salts and Ionic...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Anions for Lithium Salts and Ionic Liquids for Lithium Battery Electrolytes Inexpensive, Nonfluorinated Anions for Lithium Salts and Ionic Liquids for Lithium Battery Electrolytes...

163

Preparation of silica aerogel using ionic liquids as solvents Sheng Dai,*a Y. H. Ju,ac H. J. Gao,b J. S. Lin,b S. J. Pennycookb and C. E. Barnesc  

E-Print Network [OSTI]

Preparation of silica aerogel using ionic liquids as solvents Sheng Dai,*a Y. H. Ju,ac H. J. Gaord December 1999 Ionic liquids have been used as effective solvents to synthesize aerogels; a long aging time can be used to produce stable aerogel structures without the need for supercritical drying

Gao, Hongjun

164

The Partitioning of Americium and the Lanthanides Using Tetrabutyldiglycolamide (TBDGA) in Octanol and in Ionic Liquid Solution  

SciTech Connect (OSTI)

Separations among the lanthanides and the separation of Am from the lanthanides remain challenging, and research in this area continues to expand. The separation of adjacent lanthanides is of interest to high-tech industries because individual lanthanides have specialized uses and are in short supply. In nuclear fuel cycle applications Am would be incorporated into fast reactor fuels, yet the lanthanides are not desired. In this work the diamide N,N,N',N'-tetrabutyldiglycolamide (TBDGA) was investigated as a ligand for lanthanide and Am solvent extraction in both molecular and room temperature ionic liquid (RTIL) diluents. The RTIL [C4MIM][Tf2N-] showed very high extraction efficiency for these trivalent metals from low nitric acid concentrations, while the molecular diluent 1-octanol showed high extraction efficiency at high acid concentrations. This was attributed to the extraction of ionic nitrate complexes by the RTIL, whereas 1-octanol extracted neutral nitrate complexes. TBDGA in RTIL did not provide adequate separation factors for Am/lanthanide partitioning, but 1-octanol did show reasonable separation possibilities. Lanthanide intergroup separations appeared to be feasible in both diluents, but with higher separation factors from 1-octanol.

M.E. Mincher; D.L. Quach; Y.J. Liao; B.J. Mincher; C.M. Wai

2012-11-01T23:59:59.000Z

165

Curvature Effect on the Capacitance of Electric Double Layers at Ionic Liquid/Onion-Like Carbon Interfaces  

SciTech Connect (OSTI)

Recent experiments have revealed that onion-like carbons (OLCs) offer high energy density and charging/discharging rates when used as the electrodes in supercapacitors. To understand the physical origin of this phenomenon, molecular dynamics simulations were performed for a room-temperature ionic liquid near idealized spherical OLCs with radii ranging from 0.356 to 1.223 nm. We find that the surface charge density increases almost linearly with the potential applied on electric double layers (EDLs) near OLCs. This leads to a nearly flat shape of the differential capacitance versus the potential, unlike the bell or camel shape observed on planar electrodes. Moreover, our simulations reveal that the capacitance of EDLs on OLCs increases with the curvature or as the OLC size decreases, in agreement with experimental observations. The curvature effect is explained by dominance of charge overscreening over a wide potential range and increased ion density per unit area of electrode surface as the OLC becomes smaller.

Feng, Guang [ORNL; Jiang, Deen [ORNL; Cummings, Peter T [ORNL

2012-01-01T23:59:59.000Z

166

FRAGMENTATION OF COAL AND IMPROVED DISPERSION OF LIQUEFACTION CATALYSTS USING IONIC LIQUIDS.  

E-Print Network [OSTI]

??Coal has been utilized for coal-to-liquid fuels and coal-to-chemical industries both historically in South Africa and recently in China. Abundant bituminous and low-rank coal reserves… (more)

Cetiner, Ruveyda

2011-01-01T23:59:59.000Z

167

High-Surface-Area CO2 Sponge: High Performance CO2 Scrubbing Based on Hollow Fiber-Supported Designer Ionic Liquid Sponges  

SciTech Connect (OSTI)

IMPACCT Project: The team from ORNL and Georgia Tech is developing a new technology that will act like a sponge, integrating a new, alcohol-based ionic liquid into hollow fibers (magnified image, right) to capture CO2 from the exhaust produced by coal-fired power plants. Ionic liquids, or salts that exist in liquid form, are promising materials for carbon capture and storage, but their tendency to thicken when combined with CO2 limits their efficiency and poses a challenge for their development as a cost-effective alternative to current-generation solutions. Adding alcohol to the mix limits this tendency to thicken in the presence of CO2 but can also make the liquid more likely to evaporate, which would add significantly to the cost of CO2 capture. To solve this problem, ORNL is developing new classes of ionic liquids with high capacity for absorbing CO2. ORNL’s sponge would reduce the cost associated with the energy that would need to be diverted from power plants to capture CO2 and release it for storage.

None

2010-09-01T23:59:59.000Z

168

An innovative experimental approach aiming to understand and quantify the actual fire hazards of ionic liquids  

E-Print Network [OSTI]

access to fundamental flammability properties of these chemicals through the use of Pyrolysis Combustion to flash point values, various threshold values being considered in different regulatory frameworks to rate, in the Classification Labelling and Packaging regulation,14 flammable liquids are those having a flash point below

Paris-Sud XI, Université de

169

One electron oxygen reduction in room temperature ionic liquids: A comparative study of Butler-Volmer and Symmetric Marcus-Hush theories using microdisc electrodes  

E-Print Network [OSTI]

The voltammetry for the reduction of oxygen at a microdisc electrode is reported in two room temperature ionic liquids: 1-butyl-1-methylpyyrolidinium bis(trifluoromethylsulfonyl) imide ([Bmpyrr][NTf2]) and trihexyltetradecylphosphonium bis9trifluoromethylsulfonyl) imide ([P14,6,6,6][NTf2]) at 298 K. Simulated voltammograms using Butler-Volmer theory and Symmetric Marcus-Hush (SMH) theory were compared with experimental data. Butler-Volmer theory consistently provided experimental parameters with a higher level of certainty than SMH theory. A value of solvent reorganisation energy for oxygen reduction in ionic liquids was inferred for the first time as 0.4-0.5 eV, which is attributable to inner-sphere reorganisation with a negligible contribution from solvent reorganisation. The developed Butler-Volmer and Symmetric Marcus-Hush programs are also used to theoretically study the possibility of kinetically limited steady state currents, and to establish an approximate equivalence relationship between microdisc el...

Tanner, Eden E L; Barnes, Edward O; Compton, Richard G

2015-01-01T23:59:59.000Z

170

AGING EFFECTS ON THE PROPERTIES OF IMIDAZOLIUM, QUATERNARY AMMONIUM, PYRIDINIUM AND PYRROLIDINIUM-BASED IONIC LIQUIDS USED IN FUEL AND ENERGY PRODUCTION  

SciTech Connect (OSTI)

Ionic liquids are often cited for their excellent thermal stability, a key property for their use as solvents and in the chemical processing of biofuels. However, there has been little supporting data on the long term aging effect of temperature on these materials. Imizadolium, quaternary ammonium, pyridinium, and pyrrolidnium-based ionic liquids with the bis(trifluoromethylsulfonyl)imide and bis(perfluoroethylsulfonyl)imide anions were aged for 2520 hours (15 weeks) at 200?C in air to determine the effects of an oxidizing environment on their chemical structure and thermal stability over time. It was found that the minor changes in the cation chemistry could greatly affect the properties of the ILs over time.

Fox, E.

2013-08-13T23:59:59.000Z

171

Fluorohydrogenate Cluster Ions in the Gas Phase: Electrospray Ionization Mass Spectrometry of the [1-Ethyl-3-methylimidazolium+][F(HF)2.3–] Ionic Liquid  

SciTech Connect (OSTI)

Electrospray ionization of the fluorohydrogenate ionic liquid [1-ethyl-3-methylimidazolium][F(HF)2.3] ionic liquid was conducted to understand the nature of the anionic species as they exist in the gas phase. Abundant fluorohydrogenate clusters were produced; however, the dominant anion in the clusters was [FHF-], and not the fluoride-bound HF dimers or trimers that are seen in solution. Density functional theory (DFT) calculations suggest that HF molecules are bound to the clusters by about 30 kcal/mol. The DFT-calculated structures of the [FHF-]-bearing clusters show that the favored interactions of the anions are with the methynic and acetylenic hydrogen atoms on the imidazolium cation, forming planar structures similar to those observed in the solid state. A second series of abundant negative ions was also formed that contained [SiF5-] together with the imidazolium cation and the fluorohydrogenate anions that originate from reaction of the spray solution with silicate surfaces.

Gary S. Groenewold; James E. Delmore; Michael T. Benson; Tetsuya Tsuda; Rika Hagiwara

2013-12-01T23:59:59.000Z

172

Acidic Ionic Liquid/Water Solution as Both Medium and Proton Source for Electrocatalytic H2 Evolution by [Ni(P2N2)2]2+ Complexes  

SciTech Connect (OSTI)

The electrocatalytic reduction of protons to H2 by [Ni(PPh2NC6H4-hex2)2](BF4)2 (where PPh2NC6H4-hex2 = 1,5-di(4-n-hexylphenyl)-3,7-diphenyl-1,5-diaza-3,7-diphosphacyclooctane) in the highly acidic ionic liquid dibutylformamidium bis(trifluoromethanesulfonyl)amide shows a strong dependence on added water. A turnover frequency of 43,000-53,000 s-1 has been measured for hydrogen production at 25 °C when the mole fraction of water (?H2O) is 0.72. The same catalyst in acetonitrile with added dimethylformamidium trifluoromethanesulfonate and water has a turnover frequency of 720 s?1. Thus the use of an ionic liquid/aqueous solution enhances the observed catalytic rates by more than a factor of 50 compared to acids in traditional organic solvents such as acetonitrile. Complexes [Ni(PPh2NC6H4X2)2](BF4)2 (X = H, OMe, CH2P(O)(OEt)2, Br) are also catalysts in the ionic liquid/water mixture, and the observed catalytic rates correlate with the hydrophobicity of X. This research was supported as part of the Center for Molecular Electrocatalysis, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences. Pacific Northwest National Laboratory is operated by Battelle for the U.S. Department of Energy.

Pool, Douglas H.; Stewart, Michael P.; O'Hagan, Molly J.; Shaw, Wendy J.; Roberts, John A.; Bullock, R. Morris; DuBois, Daniel L.

2012-09-25T23:59:59.000Z

173

Nonequilibrium Thermodynamics of Porous Electrodes  

E-Print Network [OSTI]

We reformulate and extend porous electrode theory for non-ideal active materials, including those capable of phase transformations. Using principles of non-equilibrium thermodynamics, we relate the cell voltage, ionic ...

Ferguson, Todd Richard

174

Smouldering Combustion of Organic Liquids in Porous Media for Remediating NAPL-contaminated Soils   

E-Print Network [OSTI]

This research investigated the potential of smouldering combustion to be employed as a remediation approach for soil contaminated by non-aqueous phase liquids (NAPLs). Small-scale (~15 cm), proof-of-concept experiments ...

Pironi, Paolo

2010-01-01T23:59:59.000Z

175

Porous Materials Porous Materials  

E-Print Network [OSTI]

1 Porous Materials x Porous Materials · Physical properties * Characteristic impedance p = p 0 e -jk xa- = vej[ ] p x - j ; Zc= p ve = c ka 0k = c 1-j #12;2 Porous Materials · Specific acoustic impedance Porous Materials · Finite thickness ­ blocked p e + -jk (x-d)a p e - jk (x-d)a d x #12

Berlin,Technische Universität

176

A counter-charge layer in generalized solvents framework for electrical double layers in neat and hybrid ionic liquid electrolytes  

SciTech Connect (OSTI)

Room-temperature ionic liquids (RTILs) have received significant attention as electrolytes due to a number of attractive properties such as their wide electrochemical windows. Since electrical double layers (EDLs) are the cornerstone for the applications of RTILs in electrochemical systems such as supercapacitors, it is important to develop an understanding of the structure capacitance relationships for these systems. Here we present a theoretical framework termed counter-charge layer in generalized solvents (CGS) for describing the structure and capacitance of the EDLs in neat RTILs and in RTILs mixed with different mass fractions of organic solvents. Within this framework, an EDL is made up of a counter-charge layer exactly balancing the electrode charge, and of polarized generalized solvents (in the form of layers of ion pairs, each of which has a zero net charge but has a dipole moment the ion pairs thus can be considered as a generalized solvent) consisting of all RTILs inside the system except the counter-ions in the counter-charge layer, together with solvent molecules if present. Several key features of the EDLs that originate from the strong ion ion correlation in RTILs, e.g., overscreening of electrode charge and alternating layering of counter-ions and co-ions, are explicitly incorporated into this framework. We show that the dielectric screening in EDLs is governed predominately by the polarization of generalized solvents (or ion pairs) in the EDL, and the capacitance of an EDL can be related to its microstructure with few a priori assumptions or simplifications. We use this framework to understand two interesting phenomena observed in molecular dynamics simulations of EDLs in a neat IL of 1-butyl-3- methylimidazolium tetrafluoroborate ([BMIM][BF4]) and in a mixture of [BMIM][BF4] and acetonitrile (ACN): (1) the capacitance of the EDLs in the [BMIM][BF4]/ACN mixture increases only slightly when the mass fraction of ACN in the mixture increases from zero to 50% although the dielectric constant of bulk ACN is more than two times higher than that of neat [BMIM][BF4]; (2) the capacitance of EDLs near negative electrodes (with BMIM+ ion as the counter-ion) is smaller than that near positive electrodes (with BF4as counter-ion) although the closest approaches of both ions to the electrode surface are nearly identical.

Huang, Jingsong [ORNL; Feng, Guang [Clemson University; Sumpter, Bobby G [ORNL; Qiao, Rui [ORNL; Meunier, Vincent [ORNL

2011-01-01T23:59:59.000Z

177

Amine-functionalized task-specific ionic liquids: a mechanistic explanation for the dramatic increase in viscosity upon complexation with CO{sub 2} from molecular simulation  

SciTech Connect (OSTI)

The capture of CO{sub 2} from fossil fuel combustion, particularly in coal-fired power plants, represents a critical component of efforts aimed at stabilizing greenhouse gas levels in the atmosphere. Recently, a series of second-generation task-specific ionic liquids (TSILs) containing amine functional groups have been synthesized and demonstrated to have much higher capacities for CO{sub 2} due to their reactivity with CO{sub 2}, as well unusually high viscosities in both the neat and complexed states. The current work extends the seminal studies of CO{sub 2} capture with ionic liquids (ILs) by providing insight from simulations into the mechanism responsible for the dramatic increase in viscosity upon complexation. Simulations conclusively demonstrate that the slow translational and rotational dynamics, which are manifest in the high viscosity, may be attributable to the formation of a strong, pervasive hydrogen-bonded network. Semiquantitative estimates of the cation and anion self-diffusion coefficients and rotational time constants, as well as detailed hydrogen bond analysis, are consistent with the experimentally observed formation of glassy or gel-like materials upon contact with CO{sub 2}. This has significant implications for the design of new approaches or materials involving ILs that take advantage of these preconceived limitations, in the synthesis or manipulation of new TSIL frameworks for CO{sub 2} capture, and in novel experimental studies of chemistries and dynamics in persistent heterogeneous environments.

Gutowski, K.E.; Maginn, E.J. [University of Notre Dame, Notre Dame, IN (United States)

2008-11-15T23:59:59.000Z

178

IMIDAZOLE-BASED IONIC LIQUIDS FOR USE IN POLYMER ELECTROLYTE MEMBRANE FUEL CELLS: EFFECT OF ELECTRON-WITHDRAWING AND ELECTRON-DONATING SUBSTITUENTS  

SciTech Connect (OSTI)

Current polymer electrolyte membrane fuel cells (PEMFCs) require humidifi cation for acceptable proton conductivity. Development of a novel polymer that is conductive without a water-based proton carrier is desirable for use in automobiles. Imidazole (Im) is a possible replacement for water as a proton solvent; Im can be tethered to the polymer structure by means of covalent bonds, thereby providing a solid state proton conducting membrane where the solvating groups do not leach out of the fuel cell. These covalent bonds can alter the electron availability of the Im molecule. This study investigates the effects of electron-withdrawing and electron-donating substituents on the conductivity of Im complexed with methanesulfonic acid (MSA) in the form of ionic liquids. Due to the changes in the electronegativity of nitrogen, it is expected that 2-phenylimidazole (2-PhIm, electron-withdrawing) will exhibit increased conductivity compared to Im, while 2-methylimidazole (2-MeIm, electron-donating) will exhibit decreased conductivity. Three sets of ionic liquids were prepared at defi ned molar ratios: Im-MSA, 2-PhIm-MSA, and 2-MeIm- MSA. Differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and 1H-NMR were used to characterize each complex. Impedance analysis was used to determine the conductivity of each complex. Both the 2-PhIm-MSA and 2-MeIm-MSA ionic liquids were found to be less conductive than the Im-MSA complex at base-rich compositions, but more conductive at acid-rich compositions. 1H-NMR data shows a downfi eld shift of the proton on nitrogen in 2-PhIm compared to Im, suggesting that other factors may diminish the electronic effects of the electron withdrawing group at base-rich compositions. Further studies examining these effects may well result in increased conductivity for Im-based complexes. Understanding the conductive properties of Im-derivatives due to electronic effects will help facilitate the development of a new electrolyte appropriate for automotive fuel cell use.

Chang, E.; Fu, Y.; Kerr, J.

2009-01-01T23:59:59.000Z

179

Pd-porphyrin functionalized ionic liquid-modified mesoporous SBA-15: An efficient and recyclable catalyst for solvent-free Heck reaction  

SciTech Connect (OSTI)

The Pd-porphyrin functionalized ionic liquid could be covalently anchored in the channels of mesoporous SBA-15 through ion-pair electrostatic interaction between imidazolium-cationic and Pd-porphyrin-anionic moieties. Such modified SBA-15 materials were prepared successfully via a post-synthesis (surface sol-gel polymerization) or a one-pot sol-gel procedure, which were characterized by powder X-ray diffraction, UV-visible spectroscopy, Fourier transform infrared spectroscopy, N{sub 2} sorption, elemental analysis, and transmission electron microscopy. The modified SBA-15 materials are efficient and recyclable catalysts for cross-coupling of aryl iodides or activated aryl bromides with ethyl acrylate without activity loss and Pd leaching even after 9 runs.

Zhang, Jing; Zhao, Guo-Feng [Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Chemistry Department, East China Normal University, Shanghai 200062 (China)] [Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Chemistry Department, East China Normal University, Shanghai 200062 (China); Popovic, Zora [General and Inorganic Laboratory, Chemistry Department, University of Zagreb, HR-10000 Zagreb (Croatia)] [General and Inorganic Laboratory, Chemistry Department, University of Zagreb, HR-10000 Zagreb (Croatia); Lu, Yong [Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Chemistry Department, East China Normal University, Shanghai 200062 (China)] [Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Chemistry Department, East China Normal University, Shanghai 200062 (China); Liu, Ye, E-mail: yliu@chem.ecnu.edu.cn [Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Chemistry Department, East China Normal University, Shanghai 200062 (China)] [Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Chemistry Department, East China Normal University, Shanghai 200062 (China)

2010-11-15T23:59:59.000Z

180

One-pot synthesis of SnO{sub 2}/reduced graphene oxide nanocomposite in ionic liquid-based solution and its application for lithium ion batteries  

SciTech Connect (OSTI)

Graphical abstract: - Highlights: • A facile and low-temperature method is developed for SnO{sub 2}/graphene composite. • Synthesis performed in a choline chloride-based ionic liquid. • The composite shows an enhanced cycling stability as anode for Li-ion batteries. • 4 nm SnO{sub 2} nanoparticles mono-dispersed on the surface of reduced graphene oxide. - Abstract: A facile and low-temperature method is developed for SnO{sub 2}/graphene composite which involves an ultrasonic-assistant oxidation–reduction reaction between Sn{sup 2+} and graphene oxide in a choline chloride–ethylene glycol based ionic liquid under ambient conditions. The reaction solution is non-corrosive and environmental-friendly. Moreover, the proposed technique does not require complicated infrastructures and heat treatment. The SnO{sub 2}/graphene composite consists of about 4 nm sized SnO{sub 2} nanoparticles with cassiterite structure mono-dispersed on the surface of reduced graphene oxide. As anode for lithium-ion batteries, the SnO{sub 2}/graphene composite shows a satisfying cycling stability (535 mAh g{sup ?1} after 50 cycles @100 mA g{sup ?1}), which is significantly prior to the bare 4 nm sized SnO{sub 2} nanocrsytals. The graphene sheets in the hybrid nanostructure could provide a segmentation effect to alleviate the volume expansion of the SnO{sub 2} and restrain the small and active Sn-based particles aggregating into larger and inactive clusters during cycling.

Gu, Changdong, E-mail: cdgu@zju.edu.cn; Zhang, Heng; Wang, Xiuli; Tu, Jiangping

2013-10-15T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

Nonaqueous Phase Liquid Dissolution in Porous Media: Multi-Scale Effects of Multi-Component Dissolution Kinetics on Cleanup Time  

SciTech Connect (OSTI)

Industrial organic solvents such as trichloroethylene (TCE) and tetrachloroethylene (PCE) constitute a principal class of groundwater contaminants. Cleanup of groundwater plume source areas associated with these compounds is problematic, in part, because the compounds often exist in the subsurface as dense nonaqueous phase liquids (DNAPLs). Ganglia (or 'blobs') of DNAPL serve as persistent sources of contaminants that are difficult to locate and remediate (e.g. Fenwick and Blunt, 1998). Current understanding of the physical and chemical processes associated with dissolution of DNAPLs in the subsurface is incomplete and yet is critical for evaluating long-term behavior of contaminant migration, groundwater cleanup, and the efficacy of source area cleanup technologies. As such, a goal of this project has been to contribute to this critical understanding by investigating the multi-phase, multi-component physics of DNAPL dissolution using state-of-the-art experimental and computational techniques. Through this research, we have explored efficient and accurate conceptual and numerical models for source area contaminant transport that can be used to better inform the modeling of source area contaminants, including those at the LLNL Superfund sites, to re-evaluate existing remediation technologies, and to inspire or develop new remediation strategies. The problem of DNAPL dissolution in natural porous media must be viewed in the context of several scales (Khachikian and Harmon, 2000), including the microscopic level at which capillary forces, viscous forces, and gravity/buoyancy forces are manifested at the scale of individual pores (Wilson and Conrad, 1984; Chatzis et al., 1988), the mesoscale where dissolution rates are strongly influenced by the local hydrodynamics, and the field-scale. Historically, the physico-chemical processes associated with DNAPL dissolution have been addressed through the use of lumped mass transfer coefficients which attempt to quantify the dissolution rate in response to local dissolved-phase concentrations distributed across the source area using a volume-averaging approach (Figure 1). The fundamental problem with the lumped mass transfer parameter is that its value is typically derived empirically through column-scale experiments that combine the effects of pore-scale flow, diffusion, and pore-scale geometry in a manner that does not provide a robust theoretical basis for upscaling. In our view, upscaling processes from the pore-scale to the field-scale requires new computational approaches (Held and Celia, 2001) that are directly linked to experimental studies of dissolution at the pore scale. As such, our investigation has been multi-pronged, combining theory, experiments, numerical modeling, new data analysis approaches, and a synthesis of previous studies (e.g. Glass et al, 2001; Keller et al., 2002) aimed at quantifying how the mechanisms controlling dissolution at the pore-scale control the long-term dissolution of source areas at larger scales.

McNab, W; Ezzedine, S; Detwiler, R

2007-02-26T23:59:59.000Z

182

Lithium ion conducting ionic electrolytes  

DOE Patents [OSTI]

A liquid, predominantly lithium-conducting, ionic electrolyte is described which has exceptionally high conductivity at temperatures of 100.degree. C. or lower, including room temperature. It comprises molten lithium salts or salt mixtures in which a small amount of an anionic polymer lithium salt is dissolved to stabilize the liquid against recrystallization. Further, a liquid ionic electrolyte which has been rubberized by addition of an extra proportion of anionic polymer, and which has good chemical and electrochemical stability, is described. This presents an attractive alternative to conventional salt-in-polymer electrolytes which are not cationic conductors.

Angell, C. Austen (Mesa, AZ); Xu, Kang (Tempe, AZ); Liu, Changle (Tulsa, OK)

1996-01-01T23:59:59.000Z

183

Strong Electronic Polarization of the C60 Fullerene by the Imidazolium-Based Ionic Liquids: Accurate Insights from Born-Oppenheimer Molecular Dynamics Simulations  

E-Print Network [OSTI]

Fullerenes are known to be polarizable due to the strained carbon-carbon bonds and high surface curvature. Electronic polarization of fullerenes is of steady practical importance, since it leads to non-additive interactions and, therefore, to unexpected phenomena. For the first time, hybrid density functional theory (HDFT) powered Born-Oppenheimer molecular dynamics (BOMD) simulations have been conducted to observe electronic polarization and charge transfer phenomena in the C60 fullerene at finite temperature (350 K). The non-additive phenomena are fostered by the three selected imidazolium-based room-temperature ionic liquids (RTILs). We conclude that although charge transfer appears nearly negligible in these systems, an electronic polarization is indeed significant leading to a systematically positive effective electrostatic charge on the C60 fullerene: +0.14e in [EMIM][Cl], +0.21e in [EMIM][NO3], +0.17e in [EMIM][PF6]. These results are, to certain extent, unexpected providing an inspiration to consider ...

Chaban, Vitaly V

2015-01-01T23:59:59.000Z

184

Final Technical Report: SISGR: The Influence of Electrolyte Structure and Electrode Morphology on the Performance of Ionic-Liquid Based Supercapacitors: A Combined Experimental and Simulation Study  

SciTech Connect (OSTI)

Obtaining fundamental understanding and developing predictive modeling capabilities of electrochemical interfaces can significantly shorten the development cycles of electrical double layer capacitors (EDLCs). A notable improvement in EDLC performance has been achieved due to recent advances in understanding charge storage mechanisms, development of advanced nanostructured electrodes and electrochemically stable electrolytes. The development of new generation of EDLCs is intimately linked to that of nanostructured carbon materials which have large surface area, good adsorption/desorption properties, good electrical conductivity and are relatively inexpensive. To address these scientific challenges the efforts of an interdisciplinary team of modelers and experimentalists were combined to enhance our understanding of molecular level mechanisms controlling the performance of EDLCs comprised of room temperature ionic liquid (RTIL) electrolytes and nanostructured carbon-based electrodes and to utilize these knowledge in the design of a new generation of materials and devices for this energy storage application. Specifically our team efforts included: atomistic molecular dynamics simulations, materials science and electrode/device assembly, and synthesis and characterization of RTIL electrolytes.

Bedrov, Dmitry [University of Utah] [University of Utah

2013-08-15T23:59:59.000Z

185

Overlimiting Current and Shock Electrodialysis in Porous Media  

E-Print Network [OSTI]

Most electrochemical processes, such as electrodialysis, are limited by diffusion, but in porous media, surface conduction and electroosmotic flow also contribute to ionic flux. In this article, we report experimental ...

Deng, Daosheng

186

Development of a Conceptual Process for Selective CO{sub 2} Capture from Fuel Gas Streams Using [hmim][Tf2N] Ionic Liquid as a Physical Solvent  

SciTech Connect (OSTI)

The Ionic Liquid (IL) [hmim][Tf2N] was used as a physical solvent in an Aspen Plus simulation, employing the Peng-Robinson Equation of State (P-R EOS) with Boston-Mathias (BM) alpha function and standard mixing rules, to develop a conceptual process for CO{sub 2} capture from a shifted warm fuel gas stream produced from Pittsburgh # 8 coal for a 400 MWe power plant. The physical properties of the IL, including density, viscosity, surface tension, vapor pressure and heat capacity were obtained from literature and modeled as a function of temperature. Also, available experimental solubility values for CO{sub 2}, H{sub 2}, H{sub 2}S, CO, and CH{sub 4} in this IL were compiled and their binary interaction parameters ({delta}{sub ij} and l{sub ij}) were optimized and correlated as functions of temperature. The Span-Wager Equation-of-State EOS was also employed to generate CO{sub 2} solubilities in [hmim][Tf2N] at high pressures (up to 10 MPa) and temperatures (up to 510 K). The conceptual process developed consisted of 4 adiabatic absorbers (2.4 m ID, 30 m high) arranged in parallel and packed with Plastic Pall Rings of 0.025 m for CO{sub 2} capture; 3 flash drums arranged in series for solvent (IL) regeneration with the pressure-swing option; and a pressure-intercooling system for separating and pumping CO{sub 2} up to 153 bar to the sequestration sites. The compositions of all process streams, CO{sub 2} capture efficiency, and net power were calculated using Aspen Plus simulator. The results showed that, based on the composition of the inlet gas stream to the absorbers, 95.67 mol% of CO{sub 2} was captured and sent to sequestration sites; 99.5 mol% of H{sub 2} was separated and sent to turbines; the solvent exhibited a minimum loss of 0.31 mol%; and the net power balance of the entire system was 30.81 MW. These results indicated that [hmim][Tf2N] IL could be used as a physical solvent for CO{sub 2} capture from warm shifted fuel gas streams with high efficiency.

Basha, Omar M.; Keller, Murphy J.; Luebke, David R.; Resnik, Kevin; P Morsi, Badie I.

2013-07-01T23:59:59.000Z

187

Sandia National Laboratories: ionic liquid  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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188

Review of enhanced vapor diffusion in porous media  

SciTech Connect (OSTI)

Vapor diffusion in porous media in the presence of its own liquid has often been treated similar to gas diffusion. The gas diffusion rate in porous media is much lower than in free space due to the presence of the porous medium and any liquid present. However, enhanced vapor diffusion has also been postulated such that the diffusion rate may approach free-space values. Existing data and models for enhanced vapor diffusion, including those in TOUGH2, are reviewed in this paper.

Webb, S.W.; Ho, C.K.

1998-08-01T23:59:59.000Z

189

E-Print Network 3.0 - anomalous ionic conductivity Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Science 25 ORNL 2010-G00986jcn UT-B ID 200902213 Summary: . Advantages Superior thermal stability over other protic ionic liquids Proton conducting mechanism does......

190

Partially fluorinated ionic compounds  

DOE Patents [OSTI]

Partially fluorinated ionic compounds are prepared. They are useful in the preparation of partially fluorinated dienes, in which the repeat units are cycloaliphatic.

Han, legal representative, Amy Qi (Hockessin, DE); Yang, Zhen-Yu (Hockessin, DE)

2008-11-25T23:59:59.000Z

191

PUBLISHED ONLINE: 7 APRIL 2013 | DOI: 10.1038/NMAT3598 Adaptive fluid-infused porous films with tunable  

E-Print Network [OSTI]

LETTERS PUBLISHED ONLINE: 7 APRIL 2013 | DOI: 10.1038/NMAT3598 Adaptive fluid-infused porous films for malleable surfaces. As we have recently shown, a liquid infused in a rigid porous substrate develops 1School

Mahadevan, L.

192

Static dielectric properties of dense ionic fluids  

E-Print Network [OSTI]

The static dielectric properties of dense ionic fluids, e.g., room temperature ionic liquids (RTILs) and inorganic fused salts, are investigated on different length scales by means of grandcanonical Monte Carlo simulations. A generally applicable scheme is developed which allows one to approximately decompose the electric susceptibility of dense ionic fluids into the orientation and the distortion polarization contribution. It is shown that at long range the well-known plasma-like perfect screening behavior occurs, which corresponds to a diverging distortion susceptibility, whereas at short range orientation polarization dominates, which coincides with that of a dipolar fluid of attached cation-anion pairs. This observation suggests that the recently debated interpretation of RTILs as dilute electrolyte solutions might not be simply a yes-no-question but it might depend on the considered length scale.

Zarubin, Grigory

2015-01-01T23:59:59.000Z

193

Charge Compensation in RE3+ (RE = Eu, Gd) and M+ (M = Li, Na, K) Co-Doped Alkaline Earth Nanofluorides Obtained by Microwave Reaction with Reactive Ionic Liquids Leading to Improved Optical Properties  

SciTech Connect (OSTI)

Alkaline earth fluorides are extraordinarily promising host matrices for phosphor materials with regard to rare earth doping. In particular, quantum cutting materials, which might considerably enhance the efficiency of mercury-free fluorescent lamps or SC solar cells, are often based on rare earth containing crystalline fluorides such as NaGdF4, GdF3 or LaF3. Substituting most of the precious rare earth ions and simultaneously retaining the efficiency of the phosphor is a major goal. Alkaline earth fluoride nanoparticles doped with trivalent lanthanide ions (which are required for the quantum cutting phenomenon) were prepared via a microwave assisted method in ionic liquids. As doping trivalent ions into a host with divalent cations requires charge compensation, this effect was thoroughly studied by powder X-ray and electron diffraction, luminescence spectroscopy and 23Na, 139La and 19F solid state NMR spectroscopy. Monovalent alkali ions were codoped with the trivalent lanthanide ions to relieve stress and achieve a better crystallinity and higher quantum cutting abilities of the prepared material. 19F-magic angle spinning (MAS)-NMR-spectra, assisted by 19F{23Na} rotational echo double resonance (REDOR) studies, reveal distinct local fluoride environments, the populations of which are discussed in relation to spatial distribution and clustering models. In the co-doped samples, fluoride species having both Na+ and La3+ ions within their coordination sphere can be identified and quantified. This interplay of mono- and trivalent ions in the CaF2 lattice appears to be an efficient charge compensation mechanism that allows for improved performance characteristics of such co-doped phosphor materials.

Lorbeer, C [Ruhr-Universitat Bochum; Behrends, F [Westfalische Wilhelsm-Universitat Munster; Cybinska, J [Ruhr Universitat Bochum; Eckert, H [Westfalische Wilhelsm-Universitat Munster; Mudring, Anja -V [Ames Laboratory

2014-01-01T23:59:59.000Z

194

Preparation of High Purity, High Molecular-Weight Chitin from Ionic Liquids for Use as an Adsorbate for the Extraction of Uranium from Seawater (Workscope MS-FC: Fuel Cycle R&D)  

SciTech Connect (OSTI)

Ensuring a domestic supply of uranium is a key issue facing the wider implementation of nuclear power. Uranium is mostly mined in Kazakhstan, Australia, and Canada, and there are few high-grade uranium reserves left worldwide. Therefore, one of the most appealing potential sources of uranium is the vast quantity dissolved in the oceans (estimated to be 4.4 billion tons worldwide). There have been research efforts centered on finding a means to extract uranium from seawater for decades, but so far none have resulted in an economically viable product, due in part to the fact that the materials that have been successfully demonstrated to date are too costly (in terms of money and energy) to produce on the necessary scale. Ionic Liquids (salts which melt below 100{degrees}C) can completely dissolve raw crustacean shells, leading to recovery of a high purity, high molecular weight chitin powder and to fibers and films which can be spun directly from the extract solution suggesting that continuous processing might be feasible. The work proposed here will utilize the unprecedented control this makes possible over the chitin fiber a) to prepare electrospun nanofibers of very high surface area and in specific architectures, b) to modify the fiber surfaces chemically with selective extractant capacity, and c) to demonstrate their utility in the direct extraction and recovery of uranium from seawater. This approach will 1) provide direct extraction of chitin from shellfish waste thus saving energy over the current industrial process for obtaining chitin; 2) allow continuous processing of nanofibers for very high surface area fibers in an economical operation; 3) provide a unique high molecular weight chitin not available from the current industrial process leading to stronger, more durable fibers; and 4) allow easy chemical modification of the large surface areas of the fibers for appending uranyl selective functionality providing selectivity and ease of stripping. The resulting sorbent should prove economically feasible, as well as providing an overall net energy gain.

Rogers, Robin

2013-12-21T23:59:59.000Z

195

Porous silicon membranes as ultrafiltration devices: a feasibility study  

E-Print Network [OSTI]

and several liquids, and the experimental results are compared to model predictions. Hexane, ethanol, and ethanol-water mixtures permeated the porous silicon membranes as liquids at pressure differentials greater than 100 psig. The membranes exhibited much... % HNOs and 4 parts water. However, the porous silicon layers became fragile during the etching and were easy to break. Experimental results for flow tests on selected samples after chemical etching are shown in the next section. 14 GAS FLOW TESTING...

Hong, Xiangrong

1993-01-01T23:59:59.000Z

196

Liquid metal electric pump  

DOE Patents [OSTI]

An electrical pump for pumping liquid metals to high pressures in high temperature environments without the use of magnets or moving mechanical parts. The pump employs a non-porous solid electrolyte membrane, typically ceramic, specific to the liquid metal to be pumped. A DC voltage is applied across the thickness of the membrane causing ions to form and enter the membrane on the electrically positive surface, with the ions being neutralized on the opposite surface. This action provides pumping of the liquid metal from one side of the non-porous solid electrolyte membrane to the other.

Abbin, Joseph P. (Albuquerque, NM); Andraka, Charles E. (Albuquerque, NM); Lukens, Laurance L. (Albuquerque, NM); Moreno, James B. (Albuquerque, NM)

1992-01-01T23:59:59.000Z

197

Liquid metal electric pump  

DOE Patents [OSTI]

An electrical pump for pumping liquid metals to high pressures in high temperature environments without the use of magnets or moving mechanical parts. The pump employs a non-porous solid electrolyte membrane, typically ceramic, specific to the liquid metal to be pumped. A DC voltage is applied across the thickness of the membrane causing ions to form and enter the membrane on the electrically positive surface, with the ions being neutralized on the opposite surface. This action provides pumping of the liquid metal from one side of the non-porous solid electrolyte membrane to the other. 3 figs.

Abbin, J.P.; Andraka, C.E.; Lukens, L.L.; Moreno, J.B.

1992-01-14T23:59:59.000Z

198

Capture of particles in soft porous media , R. Hhler and O. Pitois  

E-Print Network [OSTI]

-height in the foam sample, using a thin glass capillary. The solid particles that we use are green fluorescent Cedex 2, France We investigate the capture of particles in soft porous media. Liquid foam constitutes foams can be considered as soft porous materials, exhibiting fine liquid channels between gas bubbles

Paris-Sud XI, Université de

199

Enhanced Gas Absorption in the Ionic Liquid 1-n-Hexyl-3-methylimidazolium Bis(trifluoromethylsulfonyl)amide ([hmim][Tf{sub 2}N]) Confined in Silica Slit Pores: A Molecular Simulation Study  

SciTech Connect (OSTI)

Two-dimensional NP{sub xy}T and isostress-osmotic (N{sub 2}P{sub xy}Tf{sub 1}) Monte Carlo simulations were used to compute the density and gas absorption properties of the ionic liquid (IL) 1-n-hexyl-3- methylimidazolium bis(Trifluoromethylsulfonyl)amide ([hmim][Tf{sub 2}N]) confined in silica slit pores (25-45 Å). Self-diffusivity values for both gas and IL were calculated from NVE molecular dynamics simulations using both smooth and atomistic potential models for the silica. Simulations show that the molar volume for [hmim][Tf{sub 2}N] confined in 25-45 Å silica slit pores are 12-31% larger than for the bulk IL at 313-573 K and 1 bar. The amounts of CO{sub 2}, H{sub 2}, and N{sub 2} absorbed in the confined IL are typically 1.1-3 times larger than in the bulk IL due to larger molar volumes for the confined IL compared to the bulk IL. The CO{sub 2}, N{sub 2}, and H{sub 2} molecules are generally absorbed close to the silica wall where the IL density is very low. This arrangement causes the self-diffusivities for these gases in the confined IL to be 2 to 8 times larger than in the bulk IL at 298-573 K. The solubility for water in the confined and bulk ILs are similar, which is likely due to strong water interactions with [hmim][Tf{sub 2}N] through hydrogen-bonding resulting in the confined IL molar volume playing a less important role in determining H{sub 2}O solubility. Water molecules were largely absorbed in the IL-rich region rather than close to the silica wall. The self-diffusivities for water correlate with the confined IL. The confined IL exhibits self-diffusivities larger than the bulk IL at lower temperatures, but smaller than the bulk IL at higher temperatures. The findings from simulations are consistent with available experimental data for similar confined IL systems.

Shi, Wei; Luebke, David R.

2013-05-07T23:59:59.000Z

200

Ionic liquids for rechargeable lithium batteries  

E-Print Network [OSTI]

conducting polymer electrochromic devices using ionicelectrochemical cells and electrochromic devices, including

Salminen, Justin; Papaiconomou, Nicolas; Kerr, John; Prausnitz, John; Newman, John

2008-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

Interfacial ionic liquids: connecting static and dynamic...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

L, Lee S S and Fenter P 2012 Real-time observations of interfacial lithiation in a metal silicide thin film J. Phys. Chem. C 116 22341-5 43 Lindahl E, Hess B and van der...

202

Ionic liquids for rechargeable lithium batteries  

E-Print Network [OSTI]

for rechargeable lithium batteries (Preliminary report,applications using lithium batteries, we must be sure thattemperature range. For lithium batteries in hybrid vehicles,

Salminen, Justin; Papaiconomou, Nicolas; Kerr, John; Prausnitz, John; Newman, John

2008-01-01T23:59:59.000Z

203

Ionic liquids for rechargeable lithium batteries  

E-Print Network [OSTI]

efficiency of dye-sensitized solar cells,’’ J. Phys. Chem.in dye-sensitized nanocrystalline solar cells,’’ J. Phys.

Salminen, Justin; Papaiconomou, Nicolas; Kerr, John; Prausnitz, John; Newman, John

2008-01-01T23:59:59.000Z

204

Ionic Liquid Pretreatment Technologies | Department of Energy  

Office of Environmental Management (EM)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) "of EnergyEnergyENERGY TAX POLICIES7.pdfFuel2007 | Department7 U.S.Department of05The830,Energyat

205

Synthesis of Ionic Liquids - Energy Innovation Portal  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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206

Sandia National Laboratories: ion-ic liquids  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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207

4/28/2010 1Porous Pavements Porous Pavements  

E-Print Network [OSTI]

-- Sturdy, attractive & reliable · Porous concrete -- Quality depends on installer · Porous asphalt Park parking lot (2008) ·! Shoreview Porous Concrete Street project (2009) ·! Troy Burne Golf Course4/28/2010 1Porous Pavements Porous Pavements for Stormwater Restoration in Urban Environments Cliff

Minnesota, University of

208

Liquid Wall Chambers  

SciTech Connect (OSTI)

The key feature of liquid wall chambers is the use of a renewable liquid layer to protect chamber structures from target emissions. Two primary options have been proposed and studied: wetted wall chambers and thick liquid wall (TLW) chambers. With wetted wall designs, a thin layer of liquid shields the structural first wall from short ranged target emissions (x-rays, ions and debris) but not neutrons. Various schemes have been proposed to establish and renew the liquid layer between shots including flow-guiding porous fabrics (e.g., Osiris, HIBALL), porous rigid structures (Prometheus) and thin film flows (KOYO). The thin liquid layer can be the tritium breeding material (e.g., flibe, PbLi, or Li) or another liquid metal such as Pb. TLWs use liquid jets injected by stationary or oscillating nozzles to form a neutronically thick layer (typically with an effective thickness of {approx}50 cm) of liquid between the target and first structural wall. In addition to absorbing short ranged emissions, the thick liquid layer degrades the neutron flux and energy reaching the first wall, typically by {approx}10 x x, so that steel walls can survive for the life of the plant ({approx}30-60 yrs). The thick liquid serves as the primary coolant and tritium breeding material (most recent designs use flibe, but the earliest concepts used Li). In essence, the TLW places the fusion blanket inside the first wall instead of behind the first wall.

Meier, W R

2011-02-24T23:59:59.000Z

209

Hollow porous-wall glass microspheres for hydrogen storage  

DOE Patents [OSTI]

A porous wall hollow glass microsphere is provided having a diameter range of between 1 to 200 microns, a density of between 1.0 to 2.0 gm/cc, a porous-wall structure having wall openings defining an average pore size of between 10 to 1000 angstroms, and which contains therein a hydrogen storage material. The porous-wall structure facilitates the introduction of a hydrogen storage material into the interior of the porous wall hollow glass microsphere. In this manner, the resulting hollow glass microsphere can provide a membrane for the selective transport of hydrogen through the porous walls of the microsphere, the small pore size preventing gaseous or liquid contaminants from entering the interior of the hollow glass microsphere.

Heung, Leung K. (Aiken, SC); Schumacher, Ray F. (Aiken, SC); Wicks, George G. (Aiken, SC)

2010-02-23T23:59:59.000Z

210

Ionic (Proton) Transport Hydrogen  

E-Print Network [OSTI]

environments - #12;Technology Options -- Ionic Transport Separation Systems Central, Semi-Central (coal/Semi-Central Systems Coal is the cheapest fuel, but requires the greatest pre-conditioning Clean-up of syngas requires Energy Systems ChevronTexaco SRI Consulting SAIC ChevronTexaco Technology Ventures #12;Performance

211

Open-cell glass crystalline porous material  

DOE Patents [OSTI]

An open-cell glass crystalline porous material made from hollow microspheres which are cenospheres obtained from fly ash, having an open-cell porosity of up to 90 vol. % is produced. The cenospheres are separated into fractions based on one or more of grain size, density, magnetic or non-magnetic, and perforated or non-perforated. Selected fractions are molded and agglomerated by sintering with a binder at a temperature below the softening temperature, or without a binder at a temperature about, or above, the softening temperature but below the temperature of liquidity. The porous material produced has an apparent density of 0.3-0.6 g/cm.sup.3, a compressive strength in the range of 1.2-3.5 MPa, and two types of openings: through-flow wall pores in the cenospheres of 0.1-30 micrometers, and interglobular voids between the cenospheres of 20-100 micrometers. The porous material of the invention has properties useful as porous matrices for immobilization of liquid radioactive waste, heat-resistant traps and filters, supports for catalysts, adsorbents and ion-exchangers.

Anshits, Alexander G. (Krasnoyarsk, RU); Sharonova, Olga M. (Krasnoyarsk, RU); Vereshchagina, Tatiana A. (Krasnoyarsk, RU); Zykova, Irina D. (Krasnoyarsk, RU); Revenko, Yurii A. (Zheleznogorsk, RU); Tretyakov, Alexander A. (Zheleznogorsk, RU); Aloy, Albert S. (Saint-Petersburg, RU); Lubtsev, Rem I. (Saint-Petersburg, RU); Knecht, Dieter A. (Idaho Falls, ID); Tranter, Troy J. (Idaho Falls, ID); Macheret, Yevgeny (Idaho Falls, ID)

2002-01-01T23:59:59.000Z

212

Ventilation of porous media  

DOE Patents [OSTI]

Methods are presented for distributing gases throughout the interstices of porous materials and removing volatile substances from the interstices of porous materials. Continuous oscillation of pressures and flows results in increased penetration of the interstices by flowing gases and increased transport of gaseous components out of the interstices. The invention is particularly useful in soil vapor extraction. 10 figures.

Neeper, D.A.

1994-02-22T23:59:59.000Z

213

Study of the simultaneous heat and mass transfer in two-dimensional porous media  

E-Print Network [OSTI]

in an unsaturated porous medium. A chronological discussion of the details of the review follows. Philip and De Vries[1] were the early investigators of the general topic of moisture migration in porous media with temperature gradients. The analysis revealed... for drying in a porous medium. The model accounted for the ca, pillary flow of the liquid phs, se and the diffusion of the vapor phase, including heat-conduction through the solid matrix. The coupled, non-linear governing equations, together...

Suh, Young Bae

1988-01-01T23:59:59.000Z

214

Preparation of asymmetric porous materials  

DOE Patents [OSTI]

A method for preparing an asymmetric porous material by depositing a porous material film on a flexible substrate, and applying an anisotropic stress to the porous media on the flexible substrate, where the anisotropic stress results from a stress such as an applied mechanical force, a thermal gradient, and an applied voltage, to form an asymmetric porous material.

Coker, Eric N. (Albuquerque, NM)

2012-08-07T23:59:59.000Z

215

Mixed ionic and electronic conducting ceramic membranes for hydrocarbon processing  

DOE Patents [OSTI]

The invention relates to mixed phase materials for the preparation of catalytic membranes which exhibit ionic and electronic conduction and which exhibit improved mechanical strength compared to single phase ionic and electronic conducting materials. The mixed phase materials are useful for forming gas impermeable membranes either as dense ceramic membranes or as dense thin films coated onto porous substrates. The membranes and materials of this invention are useful in catalytic membrane reactors in a variety of applications including synthesis gas production. One or more crystalline second phases are present in the mixed phase material at a level sufficient to enhance the mechanical strength of the mixture to provide membranes for practical application in CMRs.

Van Calcar, Pamela (Superior, CO); Mackay, Richard (Lafayette, CO); Sammells, Anthony F. (Boulder, CO)

2002-01-01T23:59:59.000Z

216

ESM of Ionic and Electrochemical Phenomena on the Nanoscale  

SciTech Connect (OSTI)

Operation of energy storage and conversion devices is ultimately controlled by series of intertwined ionic and electronic transport processes and electrochemical reactions at surfaces and interfaces, strongly mediated by strain and mechanical processes [1-4]. In a typical fuel cell, these include chemical species transport in porous cathode and anode materials, gas-solid electrochemical reactions at grains and triple-phase boundaries (TPBs), ionic and electronic flows in multicomponent electrodes, and chemical and electronic potential drops at internal interfaces in electrodes and electrolytes. All these phenomena are sensitively affected by the microstructure of materials from device level to the atomic scales as illustrated in Fig. 1. Similar spectrum of length scales and phenomena underpin operation of other energy systems including primary and secondary batteries, as well as hybrid systems such flow and metal-air/water batteries.

Kalinin, Sergei V [ORNL; Kumar, Amit [Pennsylvania State University; Balke, Nina [ORNL; McCorkle, Morgan L [ORNL; Guo, Senli [ORNL; Arruda, Thomas M [ORNL; Jesse, Stephen [ORNL

2011-01-01T23:59:59.000Z

217

Fabrication of porous silicon membranes  

E-Print Network [OSTI]

OF THE FILTER APPLICATION OF POROUS SILICON A. Density of Porous Silicon B. Stabilization of Porous Silicon Membranes C. Flow Test D. Porous Polycrystalline Silicon 54 58 62 65 vn TABLE OF CONTENTS (Continued) CHAPTER VI EXTENSIONS AND CONCLUSIONS... Membranes 13. Density Change of Porous Silicon at 125'C 14. Density Change oi' Porous Silicon at 250 C 15. Nitrogen Flow on a Porous Silicon Membrane Page 15 16 33 39 39 44 46 54 59 59 62 LIST OF FIGURES Figure 10. 12. 14. 17. 18. 19...

Yue, Wing Kong

1988-01-01T23:59:59.000Z

218

Charge transfer kinetics at the solid–solid interface in porous electrodes  

E-Print Network [OSTI]

Interfacial charge transfer is widely assumed to obey the Butler–Volmer kinetics. For certain liquid–solid interfaces, the Marcus–Hush–Chidsey theory is more accurate and predictive, but it has not been applied to porous ...

Bai, Peng

219

Examination of the fundamental relation between ionic transport and segmental relaxation in polymer electrolytes  

SciTech Connect (OSTI)

Replacing traditional liquid electrolytes by polymers will significantly improve electrical energy storage technologies. Despite significant advantages for applications in electrochemical devices, the use of solid polymer electrolytes is strongly limited by their poor ionic conductivity. The classical theory predicts that the ionic transport is dictated by the segmental motion of the polymer matrix. As a result, the low mobility of polymer segments is often regarded as the limiting factor for development of polymers with sufficiently high ionic conductivity. Here, we show that the ionic conductivity in many polymers can be strongly decoupled from their segmental dynamics, in terms of both temperature dependence and relative transport rate. Based on this principle, we developed several polymers with superionic conductivity. The observed fast ion transport suggests a fundamental difference between the ionic transport mechanisms in polymers and small molecules and provides a new paradigm for design of highly conductive polymer electrolytes.

Wang, Yangyang [ORNL; Fan, Fei [ORNL; Agapov, Alexander L [ORNL; Saito, Tomonori [ORNL; Yang, Jun [ORNL; Yu, Xiang [ORNL; Hong, Kunlun [ORNL; Mays, Jimmy [University of Tennessee, Knoxville (UTK); Sokolov, Alexei P [ORNL

2014-01-01T23:59:59.000Z

220

Porous material neutron detector  

DOE Patents [OSTI]

A neutron detector employs a porous material layer including pores between nanoparticles. The composition of the nanoparticles is selected to cause emission of electrons upon detection of a neutron. The nanoparticles have a maximum dimension that is in the range from 0.1 micron to 1 millimeter, and can be sintered with pores thereamongst. A passing radiation generates electrons at one or more nanoparticles, some of which are scattered into a pore and directed toward a direction opposite to the applied electrical field. These electrons travel through the pore and collide with additional nanoparticles, which generate more electrons. The electrons are amplified in a cascade reaction that occurs along the pores behind the initial detection point. An electron amplification device may be placed behind the porous material layer to further amplify the electrons exiting the porous material layer.

Diawara, Yacouba (Oak Ridge, TN); Kocsis, Menyhert (Venon, FR)

2012-04-10T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

Foams in porous media  

SciTech Connect (OSTI)

In 1978 a literature search on selective blocking of fluid flow in porous media was done by Professor S.S. Marsden and two of his graduate students, Tom Elson and Kern Huppy. This was presented as SUPRI Report No. TR-3 entitled ''Literature Preview of the Selected Blockage of Fluids in Thermal Recovery Projects.'' Since then a lot of research on foam in porous media has been done on the SUPRI project and a great deal of new information has appeared in the literature. Therefore we believed that a new, up-to-date search should be done on foam alone, one which would be helpful to our students and perhaps of interest to others. This is a chronological survey showing the development of foam flow, blockage and use in porous media, starting with laboratory studies and eventually getting into field tests and demonstrations. It is arbitrarily divided into five-year time periods. 81 refs.

Marsden, S.S.

1986-07-01T23:59:59.000Z

222

Solid oxide fuel cells having porous cathodes infiltrated with oxygen-reducing catalysts  

DOE Patents [OSTI]

Solid-oxide fuel cells include an electrolyte and an anode electrically coupled to a first surface of the electrolyte. A cathode is provided, which is electrically coupled to a second surface of the electrolyte. The cathode includes a porous backbone having a porosity in a range from about 20% to about 70%. The porous backbone contains a mixed ionic-electronic conductor (MIEC) of a first material infiltrated with an oxygen-reducing catalyst of a second material different from the first material.

Liu, Meilin; Liu, Ze; Liu, Mingfei; Nie, Lifang; Mebane, David Spencer; Wilson, Lane Curtis; Surdoval, Wayne

2014-08-12T23:59:59.000Z

223

A model for enhanced fluid percolation in porous media by application of low-frequency elastic waves  

E-Print Network [OSTI]

, primarily in connection with the appli- cations to enhanced oil recovery (EOR) and remediation of nonaqueousA model for enhanced fluid percolation in porous media by application of low-frequency elastic can significantly enhance transport of nonaqueous phase liquids (NAPLs) in porous media. Our analyses

Beresnev, Igor

224

Excitations of superfluid 4 He in porous media: Aerogel and Vycor  

E-Print Network [OSTI]

Excitations of superfluid 4 He in porous media: Aerogel and Vycor O. Plantevin and B. Fa structure factor S(Q, ) and the elementary excitations of liquid 4 He immersed in aerogel and Vycor. In both and superfluid density, S(T), of liquid 4 He in aerogel and Vycor have been made over the past 30 years.1

Glyde, Henry R.

225

Radiative heat transfer in porous uranium dioxide  

SciTech Connect (OSTI)

Due to low thermal conductivity and high emissivity of UO{sub 2}, it has been suggested that radiative heat transfer may play a significant role in heat transfer through pores of UO{sub 2} fuel. This possibility was computationally investigated and contribution of radiative heat transfer within pores to overall heat transport in porous UO{sub 2} quantified. A repeating unit cell was developed to model approximately a porous UO{sub 2} fuel system, and the heat transfer through unit cells representing a wide variety of fuel conditions was calculated using a finite element computer program. Conduction through solid fuel matrix as wekk as pore gas, and radiative exchange at pore surface was incorporated. A variety of pore compositions were investigated: porosity, pore size, shape and orientation, temperature, and temperature gradient. Calculations were made in which pore surface radiation was both modeled and neglected. The difference between yielding the integral contribution of radiative heat transfer mechanism to overall heat transport. Results indicate that radiative component of heat transfer within pores is small for conditions representative of light water reactor fuel, typically less than 1% of total heat transport. It is much larger, however, for conditions present in liquid metal fast breeder reactor fuel; during restructuring of this fuel type early in life, the radiative heat transfer mode was shown to contribute as much as 10-20% of total heat transport in hottest regions of fuel.

Hayes, S.L. [Texas A and M Univ., College Station, TX (United States)] [Texas A and M Univ., College Station, TX (United States)

1992-12-01T23:59:59.000Z

226

Asymmetric Framework for Predicting Liquid-Liquid Equilibrium of Ionic Liquid-Mixed Solvent Systems  

E-Print Network [OSTI]

of multicomponent (ternary) LLE data with conventional excess Gibbs free energy models such as NRTL.6-14 Previously, we have studied15 the capability of such models, specifically NRTL, UNIQUAC and electrolyte-NRTL (eNRTL is the NRTL-SAC (NRTL Segm

Stadtherr, Mark A.

227

Liquid-Liquid Extraction Processes  

E-Print Network [OSTI]

Liquid-liquid extraction is the separation of one or more components of a liquid solution by contact with a second immiscible liquid called the solvent. If the components in the original liquid solution distribute themselves differently between...

Fair, J. R.; Humphrey, J. L.

1983-01-01T23:59:59.000Z

228

Fabricating solid carbon porous electrodes from powders  

DOE Patents [OSTI]

Fabrication of conductive solid porous carbon electrodes for use in batteries, double layer capacitors, fuel cells, capacitive dionization, and waste treatment. Electrodes fabricated from low surface area (<50 m.sup.2 /gm) graphite and cokes exhibit excellent reversible lithium intercalation characteristics, making them ideal for use as anodes in high voltage lithium insertion (lithium-ion) batteries. Electrodes having a higher surface area, fabricated from powdered carbon blacks, such as carbon aerogel powder, carbon aerogel microspheres, activated carbons, etc. yield high conductivity carbon compositives with excellent double layer capacity, and can be used in double layer capacitors, or for capacitive deionization and/or waste treatment of liquid streams. By adding metallic catalysts to be high surface area carbons, fuel cell electrodes can be produced.

Kaschmitter, James L. (Pleasanton, CA); Tran, Tri D. (Livermore, CA); Feikert, John H. (Livermore, CA); Mayer, Steven T. (San Leandro, CA)

1997-01-01T23:59:59.000Z

229

Fabricating solid carbon porous electrodes from powders  

DOE Patents [OSTI]

Fabrication is described for conductive solid porous carbon electrodes for use in batteries, double layer capacitors, fuel cells, capacitive deionization, and waste treatment. Electrodes fabricated from low surface area (<50 m{sup 2}/gm) graphite and cokes exhibit excellent reversible lithium intercalation characteristics, making them ideal for use as anodes in high voltage lithium insertion (lithium-ion) batteries. Electrodes having a higher surface area, fabricated from powdered carbon blacks, such as carbon aerogel powder, carbon aerogel microspheres, activated carbons, etc. yield high conductivity carbon composites with excellent double layer capacity, and can be used in double layer capacitors, or for capacitive deionization and/or waste treatment of liquid streams. By adding metallic catalysts to high surface area carbons, fuel cell electrodes can be produced. 1 fig.

Kaschmitter, J.L.; Tran, T.D.; Feikert, J.H.; Mayer, S.T.

1997-06-10T23:59:59.000Z

230

Experimental and Modeling Studies of Two-Phase Flow in Porous Media and Its Effects on the Performance of a PEM Fuel Cell  

E-Print Network [OSTI]

An experimental investigation was conducted to study the two-phase flow properties of porous media used in proton exchange membrane (PEM) fuel cells. The liquid and gas phase relative permeability of porous media used in PEM fuel cells was measured...

Wang, Xuhai

2010-01-01T23:59:59.000Z

231

Porous substrates filled with nanomaterials  

DOE Patents [OSTI]

A composition comprising: at least one porous carbon monolith, such as a carbon aerogel, comprising internal pores, and at least one nanomaterial, such as carbon nanotubes, disposed uniformly throughout the internal pores. The nanomaterial can be disposed in the middle of the monolith. In addition, a method for making a monolithic solid with both high surface area and good bulk electrical conductivity is provided. A porous substrate having a thickness of 100 microns or more and comprising macropores throughout its thickness is prepared. At least one catalyst is deposited inside the porous substrate. Subsequently, chemical vapor deposition is used to uniformly deposit a nanomaterial in the macropores throughout the thickness of the porous substrate. Applications include electrical energy storage, such as batteries and capacitors, and hydrogen storage.

Worsley, Marcus A.; Baumann, Theodore F.; Satcher, Jr., Joe H.; Stadermann, Michael

2014-08-19T23:59:59.000Z

232

Filter casting nanoscale porous materials  

DOE Patents [OSTI]

A method of producing nanoporous material includes the steps of providing a liquid, providing nanoparticles, producing a slurry of the liquid and the nanoparticles, removing the liquid from the slurry, and producing monolith.

Hayes, Joel Ryan; Nyce, Gregory Walker; Kuntz, Jushua David

2013-12-10T23:59:59.000Z

233

Partially fluorinated cyclic ionic polymers and membranes  

DOE Patents [OSTI]

Ionic polymers are made from selected partially fluorinated dienes, in which the repeat units are cycloaliphatic. The polymers are formed into membranes.

Yang, Zhen-Yu

2013-04-09T23:59:59.000Z

234

Scaling of bubble growth in a porous medium. Topical report  

SciTech Connect (OSTI)

Processes involving liquid-to-gas phase change in porous media are routinely encountered, for example in the recovery of oil, geothermal processes, nuclear waste disposal or enhanced heat transfer. They involve diffusion (and convection) in the pore space, driven by an imposed supersaturation in pressure or temperature. Phase change proceeds by nucleation and phase growth. Depending on pore surface roughness, a number of nucleation centers exist, thus phase growth occurs from a multitude of clusters. Contrary to growth in the bulk or in a Hele-Shaw cell, however, growth patterns in porous media are disordered and not compact. As in immiscible displacements, they reflect the underlying pore microstructure. The competition between multiple clusters is also different from the bulk. For example, cluster growth may be controlled by a combination of diffusion (e.g. Laplace equation in the quasi-static case) with percolation. Novel growth patterns axe expected from this competition. While multiple cluster growth is important, the simpler problem of single-bubble growth is still not well understood. In this section, we focus on the growth of a single bubble, subject to a fixed far-field supersaturation (e.g. by lowering the pressure in a supersaturated solution or by raising the temperature in a. superheated liquid). Our emphasis is on deriving a scaling theory for growth at conditions of quasi-static diffusion, guided by recent experimental observations. Visualization of bubble growth in model porous media was recently conducted using 2-D etched-glass micromodels.

Satik, C.; Yortsos, Y.; Li, X. [Univ. of Southern California, Los Angeles, CA (United States). Dept. of Chemical Engineering

1995-07-01T23:59:59.000Z

235

Dispenser Printed Zinc Microbattery with an Ionic Liquid Gel Electrolyte  

E-Print Network [OSTI]

using dispenser printing including (a) 3D polymer molds, (b)using dispenser printing including (a) 3D polymer molds, (b)

Ho, Christine Chihfan

2010-01-01T23:59:59.000Z

236

Dispenser Printed Zinc Microbattery with an Ionic Liquid Gel Electrolyte  

E-Print Network [OSTI]

17 1.13. A monolithic solid-state battery formed by (a) coldcells of “monolithic” solid-state battery materials tailored1.13. A monolithic solid-state battery formed by (a) cold

Ho, Christine Chihfan

2010-01-01T23:59:59.000Z

237

Dispenser Printed Zinc Microbattery with an Ionic Liquid Gel Electrolyte  

E-Print Network [OSTI]

Fuel Cells, and Supercapacitors? ” Chem. Rev. 104, no. 10 (c-d) of origami folded supercapacitors [In, et al. ,electrodes for thin-film supercapacitors." Journal of Power

Ho, Christine Chihfan

2010-01-01T23:59:59.000Z

238

Ionic Liquids as Solvents for Catalytic Conversion of Lignocellulosic Feedstocks  

E-Print Network [OSTI]

Yoshida, Industrial & Engineering Chemistry Research [21] G.Industrial and Engineering Chemistry 1945, 37, 43-52; B.Yoshida, Industrial & Engineering Chemistry Research 2007,

Dee, Sean Joseph

2012-01-01T23:59:59.000Z

239

Tunable wavelength soft photoionization of ionic liquid vapors  

E-Print Network [OSTI]

LiTFSI and acetamide for lithium batteries. Electrochemistrysuch as fuel cells, 3-5 batteries 6,7 and solar cells. 8,9

Strasser, Daniel

2010-01-01T23:59:59.000Z

240

Dispenser Printed Zinc Microbattery with an Ionic Liquid Gel Electrolyte  

E-Print Network [OSTI]

thin-film rechargeable batteries. Materials Science andMicroscopic Nickel-Zinc Batteries for Use in AutonomousM, and RJ Brodd. “What Are Batteries, Fuel Cells, and

Ho, Christine Chihfan

2010-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


241

Tunable wavelength soft photoionization of ionic liquid vapors  

E-Print Network [OSTI]

Nevertheless, small binding enrgy shifts are evident in thea similar trend of binding enrgy shifts observed for peak

Strasser, Daniel

2010-01-01T23:59:59.000Z

242

Dispenser Printed Zinc Microbattery with an Ionic Liquid Gel Electrolyte  

E-Print Network [OSTI]

Glassy materials for lithium batteries: electrochemicalal. "Solid-state microscale lithium batteries prepared withSolid-State Rechargeable Lithium Batteries." Journal of The

Ho, Christine Chihfan

2010-01-01T23:59:59.000Z

243

Ion Transport in Nanostructured Block Copolymer/Ionic Liquid Membranes  

E-Print Network [OSTI]

14-18 fuel cells, 19-26 dye-sensitized solar cells, 27, 28batteries or dye-sensitized solar cells. 57, 58 PVdF-co-PHFP

Hoarfrost, Megan Lane

2012-01-01T23:59:59.000Z

244

Fast diffusion in a room temperature ionic liquid confined in...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

1(a) , E. Mamontov 1 , S. Dai 2 , X. Wang 2(b) , P. F. Fulvio 2 and D. J. Wesolowski 2 1 Neutron Scattering Science Division, Oak Ridge National Laboratory - Oak Ridge, TN 37831,...

245

Examination of Coal Solubility and Fragmentation with Various Ionic Liquids.  

E-Print Network [OSTI]

??The organic component of coal is heterogeneous and often has a complicated networkstructure. When exposed to certain solvents, swelling and partial dissolution often occurs.However, due… (more)

Pulati, Nuerxida

2011-01-01T23:59:59.000Z

246

Molecular dynamics modeling of ionic liquids in electrospray propulsion  

E-Print Network [OSTI]

Micro-propulsion has been studied for many years due to its applications in small-to-medium sized spacecraft for precise satellite attitude control. Electrospray thrusters are promising thrusters built upon the state of ...

Takahashi, Nanako

2010-01-01T23:59:59.000Z

247

Dispenser Printed Zinc Microbattery with an Ionic Liquid Gel Electrolyte  

E-Print Network [OSTI]

Ink-jet printed carbon supercapacitor electrodes on gold,Ink-jet printed carbon supercapacitor electrodes on gold,Microcapacitors Thin film supercapacitor (TFSC) research has

Ho, Christine Chihfan

2010-01-01T23:59:59.000Z

248

Dispenser Printed Zinc Microbattery with an Ionic Liquid Gel Electrolyte  

E-Print Network [OSTI]

Journal of Microelectromechanical Systems 16, no. 4 (JanMEMS." Journal of Microelectromechanical Systems 14, no. 5 (Journal of Microelectromechanical Systems 14, no. 2 (Jan

Ho, Christine Chihfan

2010-01-01T23:59:59.000Z

249

Ultrastable Superbase-Derived Protic Ionic Liquids - Energy Innovation  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear SecurityTensile Strain Switched Ferromagnetism in Layeredof2014 EIAUltrafast

250

Using Ionic Liquids to Make Titanium Dioxide Nanotubes - Energy Innovation  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear SecurityTensile Strain Switched Ferromagnetism inS-4500II Field Emission SEMUsedUser

251

Ionic Liquid Pretreatment Process for Biomass Is Successfully Implemented  

Broader source: Energy.gov (indexed) [DOE]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) "of EnergyEnergyENERGYWomentheATLANTA,Fermi NationalBusinessDepartmentat Larger Scale | Department of

252

New Ionic Liquids with Diverse Properties - Energy Innovation Portal  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administration the Contributions andDataNational Library of1,Department ofNewof NO2:Storage Energy

253

Carbon Films Produced from Ionic Liquid Precursors - Energy Innovation  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed New Substation Sites Proposed Route BTRICGEGR-N-CapturePortal Carbon Films

254

Ionic Liquids as Solvents for Catalytic Conversion of Lignocellulosic Feedstocks  

E-Print Network [OSTI]

cellulose, hemicellulose, and lignin. Since cellulose is theto the interaction of lignin with the biopolymers in rawthat the presence of lignin did not have a detrimental

Dee, Sean Joseph

2012-01-01T23:59:59.000Z

255

We have created a new family of ionic-liquid  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear SecurityTensile Strain Switched FerromagnetismWaste and Materials Disposition3 WaterFebruary 18, 20141Wayne J.tails

256

Thermophilic Cellulases Compatible with Ionic Liquid Pretreatment - Energy  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear SecurityTensile Strain Switched Ferromagnetism in Layered NbS2 andThe1 MembersStability ofXPS.SolidInnovation

257

Fractionation and Removal of Solutes from Ionic Liquids - Energy Innovation  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsing ZirconiaPolicyFeasibilityFieldMinds" Give Forms (AllKurt'sKinneeffects

258

Ionic Liquid Sorbents for Carbon Capture - Energy Innovation Portal  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFunInfrared LandResponsesIon/Surface Reactions and Ion Soft-Landing.Oxford

259

Ionic Liquids as Lubricants or Additives - Energy Innovation Portal  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFunInfrared LandResponsesIon/Surface Reactions and Ion

260

Project Profile: Thermally-Stable Ionic Liquid Carriers for  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

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Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

New Structure found at Ionic Liquid Surface | Center for Gas  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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262

Sandia National Laboratories: imidazolium-based ionic liquid pretreatment  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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263

Sandia National Laboratories: ionic liquids biological-ly derived from  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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264

Sandia National Laboratories: ionic-liquid mixed feedstock processing  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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265

Elucidating graphene - Ionic Liquid interfacial region: a combined  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsing Zirconia Nanoparticles asSecond stage of the longwave ICRCCM3:Else

266

Inexpensive, Nonfluorinated Anions for Lithium Salts and Ionic Liquids for  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious Rank EERE:YearRound-UpHeatMulti-Dimensionalthe U.S.Indiana College ProvidesSteamLightingSalts and

267

Ionic Liquids as Multifunctional Ashless Additives for Engine Lubrication |  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious Rank EERE:YearRound-UpHeatMulti-Dimensionalthe10 DOE VehicleStationaryLaboratory, TreeInvesting in

268

Ionic Liquids as Novel Engine Lubricants or Lubricant Additives |  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious Rank EERE:YearRound-UpHeatMulti-Dimensionalthe10 DOE VehicleStationaryLaboratory, TreeInvesting inDepartment

269

Ionic Liquids as Novel Lubricants and Additives | Department of Energy  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

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270

Computational Study of Ionic Liquids | netl.doe.gov  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation Proposed New SubstationCleanCommunity2 Computational Physics and MethodsIf you

271

Nanoparticle-Enhanced Ionic Liquids (NEILs) - Energy Innovation Portal  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administration the Contributions andData andFleet TestAccountsNanoparticle ResearchPhosphorylatedSolar

272

Spheroid-Encapsulated Ionic Liquids for Gas Separation - Energy Innovation  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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273

Dispenser Printed Zinc Microbattery with an Ionic Liquid Gel Electrolyte  

E-Print Network [OSTI]

and zinc foil electrode. The EIS scans were recorded at theand zinc foil electrode. The EIS scans were recorded at the159 9.3.1 EIS Equivalent Electrical Circuit

Ho, Christine Chihfan

2010-01-01T23:59:59.000Z

274

Fuel cell with interdigitated porous flow-field  

DOE Patents [OSTI]

A polymer electrolyte membrane (PEM) fuel cell is formed with an improved system for distributing gaseous reactants to the membrane surface. A PEM fuel cell has an ionic transport membrane with opposed catalytic surfaces formed thereon and separates gaseous reactants that undergo reactions at the catalytic surfaces of the membrane. The fuel cell may also include a thin gas diffusion layer having first and second sides with a first side contacting at least one of the catalytic surfaces. A macroporous flow-field with interdigitated inlet and outlet reactant channels contacts the second side of the thin gas diffusion layer for distributing one of the gaseous reactants over the thin gas diffusion layer for transport to an adjacent one of the catalytic surfaces of the membrane. The porous flow field may be formed from a hydrophilic material and provides uniform support across the backside of the electrode assembly to facilitate the use of thin backing layers. 9 figs.

Wilson, M.S.

1997-06-24T23:59:59.000Z

275

Fuel cell with interdigitated porous flow-field  

DOE Patents [OSTI]

A polymer electrolyte membrane (PEM) fuel cell is formed with an improved system for distributing gaseous reactants to the membrane surface. A PEM fuel cell has an ionic transport membrane with opposed catalytic surfaces formed thereon and separates gaseous reactants that undergo reactions at the catalytic surfaces of the membrane. The fuel cell may also include a thin gas diffusion layer having first and second sides with a first side contacting at least one of the catalytic surfaces. A macroporous flow-field with interdigitated inlet and outlet reactant channels contacts the second side of the thin gas diffusion layer for distributing one of the gaseous reactants over the thin gas diffusion layer for transport to an adjacent one of the catalytic surfaces of the membrane. The porous flow field may be formed from a hydrophilic material and provides uniform support across the backside of the electrode assembly to facilitate the use of thin backing layers.

Wilson, Mahlon S. (Los Alamos, NM)

1997-01-01T23:59:59.000Z

276

Foam Transport in Porous Media - A Review  

SciTech Connect (OSTI)

Amendment solutions with or without surfactants have been used to remove contaminants from soil. However, it has drawbacks such that the amendment solution often mobilizes the plume, and its movement is controlled by gravity and preferential flow paths. Foam is an emulsion-like, two-phase system in which gas cells are dispersed in a liquid and separated by thin liquid films called lamellae. Potential advantages of using foams in sub-surface remediation include providing better control on the volume of fluids injected, uniformity of contact, and the ability to contain the migration of contaminant laden liquids. It is expected that foam can serve as a carrier of amendments for vadose zone remediation, e.g., at the Hanford Site. As part of the U.S. Department of Energy’s EM-20 program, a numerical simulation capability will be added to the Subsurface Transport Over Multiple Phases (STOMP) flow simulator. The primary purpose of this document is to review the modeling approaches of foam transport in porous media. However, as an aid to understanding the simulation approaches, some experiments under unsaturated conditions and the processes of foam transport are also reviewed. Foam may be formed when the surfactant concentration is above the critical micelle concentration. There are two main types of foams – the ball foam (microfoam) and the polyhedral foam. The characteristics of bulk foam are described by the properties such as foam quality, texture, stability, density, surface tension, disjoining pressure, etc. Foam has been used to flush contaminants such as metals, organics, and nonaqueous phase liquids from unsaturated soil. Ball foam, or colloidal gas aphrons, reportedly have been used for soil flushing in contaminated site remediation and was found to be more efficient than surfactant solutions on the basis of weight of contaminant removed per gram of surfactant. Experiments also indicate that the polyhedral foam can be used to enhance soil remediation. The transport of foam in porous media is complicated in that the number of lamellae present governs flow characteristics such as viscosity, relative permeability, fluid distribution, and interactions between fluids. Hence, foam is a non-Newtonian fluid. During transport, foam destruction and formation occur. The net result of the two processes determines the foam texture (i.e., bubble density). Some of the foam may be trapped during transport. According to the impacts of the aqueous and gas flow rates, foam flow generally has two regimes – weak and strong foam. There is also a minimum pressure gradient to initiate foam flow and a critical capillary for foam to be sustained. Similar to other fluids, the transport of foam is described by Darcy’s law with the exception that the foam viscosity is variable. Three major approaches to modeling foam transport in porous media are the empirical, semi-empirical, and mechanistic methods. Mechanistic approaches can be complete in principal but may be difficult to obtain reliable parameters, whereas empirical and semi-empirical approaches can be limited by the detail used to describe foam rheology and mobility. Mechanistic approaches include the bubble population-balance model, the network/percolation theory, the catastrophe theory, and the filtration theory. Among these methods, all were developed for modeling polyhedral foam with the exception that the method based on the filtration theory was for the ball foam (microfoam).

Zhang, Z. F.; Freedman, Vicky L.; Zhong, Lirong

2009-11-11T23:59:59.000Z

277

Process of preparing tritiated porous silicon  

DOE Patents [OSTI]

A process of preparing tritiated porous silicon is described in which porous silicon is equilibrated with a gaseous vapor containing HT/T{sub 2} gas in a diluent for a time sufficient for tritium in the gas phase to replace hydrogen present in the pore surfaces of the porous silicon. 1 fig.

Tam, S.W.

1997-02-18T23:59:59.000Z

278

Process of preparing tritiated porous silicon  

DOE Patents [OSTI]

A process of preparing tritiated porous silicon in which porous silicon is equilibrated with a gaseous vapor containing HT/T.sub.2 gas in a diluent for a time sufficient for tritium in the gas phase to replace hydrogen present in the pore surfaces of the porous silicon.

Tam, Shiu-Wing (Downers Grove, IL)

1997-01-01T23:59:59.000Z

279

Metal recovery from porous materials  

DOE Patents [OSTI]

A method for recovering plutonium and other metals from materials by leaching comprising the steps of incinerating the materials to form a porous matrix as the residue of incineration, immersing the matrix into acid in a microwave-transparent pressure vessel, sealing the pressure vessel, and applying microwaves so that the temperature and the pressure in the pressure vessel increase. The acid for recovering plutonium can be a mixture of HBF.sub.4 and HNO.sub.3 and preferably the pressure is increased to at least 100 PSI and the temperature to at least 200.degree. C. The porous material can be pulverized before immersion to further increase the leach rate.

Sturcken, Edward F. (P.O. Box 900, Isle of Palms, SC 29451)

1992-01-01T23:59:59.000Z

280

Infrared spectroscopy of ionic clusters  

SciTech Connect (OSTI)

This thesis describes new experiments wherein the infrared vibrational predissociation spectra of a number of mass-selected ionic cluster systems have been obtained and analyzed in the 2600 to 4000 cm{sup {minus}1} region. The species studied include: the hydrated hydronium ions, H{sub 3}O{sup +} (H{sub 2}O){sub 3 {minus}10}, ammoniated ammonium ions, NH{sub 4}{sup +}(NH{sub 3}){sub 1 {minus}10} and cluster ions involving both water and ammonia around an ammonium ion core, (mixed clusters) NH{sub 4}{sup +}(NH{sub 3}){sub n}(H{sub 2}O){sub m} (n+m=4). In each case, the spectra reveal well resolved structures that can be assigned to transitions arising from the vibrational motions of both the ion core of the clusters and the surrounding neutral solvent molecules. 154 refs., 19 figs., 8 tabs.

Price, J.M. (California Univ., Berkeley, CA (USA). Dept. of Chemistry Lawrence Berkeley Lab., CA (USA))

1990-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

Method of preparing thin porous sheets of ceramic material  

DOE Patents [OSTI]

A method of forming thin porous sheets of ceramic material for use as electrodes or other components in a molten carbonate fuel cell is disclosed. The method involves spray drying a slurry of fine ceramic particles in liquid carrier to produce generally spherical agglomerates of high porosity and a rough surface texture. The ceramic particles may include the electrode catalyst and the agglomerates can be calcined to improve mechanical strength. After slurrying with suitable volatile material and binder tape casting is used to form sheets that are sufficiently strong for further processing and handling in the assembly of a high temperature fuel cell.

Swarr, Thomas E. (South Windsor, CT); Nickols, Richard C. (East Hartford, CT); Krasij, Myron (Avon, CT)

1987-03-24T23:59:59.000Z

282

Metal recovery from porous materials  

DOE Patents [OSTI]

The present invention relates to recovery of metals. More specifically, the present invention relates to the recovery of plutonium and other metals from porous materials using microwaves. The United States Government has rights in this invention pursuant to Contract No. DE-AC09-89SR18035 between the US Department of Energy and Westinghouse Savannah River Company.

Sturcken, E.F.

1991-01-01T23:59:59.000Z

283

Homogenization of the Poisson-Nernst-Planck Equations for Ion Transport in Charged Porous Media  

E-Print Network [OSTI]

Effective Poisson-Nernst-Planck (PNP) equations are derived for macroscopic ion transport in charged porous media under periodic fluid flow by an asymptotic multi-scale expansion with drift. The microscopic setting is a two-component periodic composite consisting of a dilute electrolyte continuum (described by standard PNP equations) and a continuous dielectric matrix, which is impermeable to the ions and carries a given surface charge. Four new features arise in the upscaled equations: (i) the effective ionic diffusivities and mobilities become tensors, related to the microstructure; (ii) the effective permittivity is also a tensor, depending on the electrolyte/matrix permittivity ratio and the ratio of the Debye screening length to the macroscopic length of the porous medium; (iii) the microscopic fluidic convection is replaced by a diffusion-dispersion correction in the effective diffusion tensor; and (iv) the surface charge per volume appears as a continuous "background charge density", as in classical membrane models. The coefficient tensors in the upscaled PNP equations can be calculated from periodic reference cell problems. For an insulating solid matrix, all gradients are corrected by the same tensor, and the Einstein relation holds at the macroscopic scale, which is not generally the case for a polarizable matrix, unless the permittivity and electric field are suitably defined. In the limit of thin double layers, Poisson's equation is replaced by macroscopic electroneutrality (balancing ionic and surface charges). The general form of the macroscopic PNP equations may also hold for concentrated solution theories, based on the local-density and mean-field approximations. These results have broad applicability to ion transport in porous electrodes, separators, membranes, ion-exchange resins, soils, porous rocks, and biological tissues.

Markus Schmuck; Martin Z. Bazant

2014-07-14T23:59:59.000Z

284

Drying by Cavitation and Poroelastic Relaxations in Porous Media with Macroscopic Pores Connected by Nanoscale Throats  

E-Print Network [OSTI]

We investigate the drying dynamics of porous media with two pore diameters separated by several orders of magnitude. Nanometer-sized pores at the edge of our samples prevent air entry, while drying proceeds by heterogeneous nucleation of vapor bubbles (cavitation) in the liquid in micrometer-sized voids within the sample. We show that the dynamics of cavitation and drying are set by the interplay of the deterministic poroelastic mass transport in the porous medium and the stochastic nucleation process. Spatio-temporal patterns emerge in this unusual reaction-diffusion system, with temporal oscillations in the drying rate and variable roughness of the drying front.

Olivier Vincent; David A. Sessoms; Erik J. Huber; Jules Guioth; Abraham D. Stroock

2014-09-30T23:59:59.000Z

285

Ionic conductors for solid oxide fuel cells  

DOE Patents [OSTI]

An electrolyte that operates at temperatures ranging from 600.degree. C. to 800.degree. C. is provided. The electrolyte conducts charge ionically as well as electronically. The ionic conductors include molecular framework structures having planes or channels large enough to transport oxides or hydrated protons and having net-positive or net-negative charges. Representative molecular framework structures include substituted aluminum phosphates, orthosilicates, silicoaluminates, cordierites, apatites, sodalites, and hollandites.

Krumpelt, Michael (Naperville, IL); Bloom, Ira D. (Bolingbrook, IL); Pullockaran, Jose D. (Hanover Park, IL); Myles, Kevin M. (Downers Grove, IL)

1993-01-01T23:59:59.000Z

286

Modification of Deeply Buried Hydrophobic Interfaces by Ionic Surfactants  

SciTech Connect (OSTI)

Hydrophobicity, the spontaneous segregation of oil and water, can be modified by surfactants. The way this modification occurs is studied at the oil-water interface for a range of alkanes and two ionic surfactants. A liquid interfacial monolayer, consisting of a mixture of alkane molecules and surfactant tails, is found. Upon cooling, it freezes at T{sub s}, well above the alkane's bulk freezing temperature, T{sub b}. The monolayer's phase diagram, derived by surface tensiometry, is accounted for by a mixtures-based theory. The monolayer's structure is measured by high-energy X-ray reflectivity above and below T{sub s}. A solid-solid transition in the frozen monolayer, occurring approximately 3 C below T{sub s}, is discovered and tentatively suggested to be a rotator-to-crystal transition.

Ocko, B.M.; Tamam, L.; Pontoni, D.; Sapir, Z.; Yefet, S.; Sloutskin, E.; Reichert, H.; Deutsch, M.

2011-04-05T23:59:59.000Z

287

Modification of Deeply Buried Hydrophobic Interfaces by Ionic Surfactants  

SciTech Connect (OSTI)

Hydrophobicity, the spontaneous segregation of oil and water, can be modified by surfactants. The way this modification occurs is studied at the oil-water interface for a range of alkanes and two ionic surfactants. A liquid interfacial monolayer, consisting of a mixture of alkane molecules and surfactant tails, is found. Upon cooling, it freezes at T{sub s}, well above the alkane's bulk freezing temperature, T{sub b}. The monolayer's phase diagram, derived by surface tensiometry, is accounted for by a mixtures-based theory. The monolayer's structure is measured by high-energy X-ray reflectivity above and below T{sub s}. A solid-solid transition in the frozen monolayer, occurring approximately 3 C below T{sub s}, is discovered and tentatively suggested to be a rotator-to-crystal transition.

L Tamam; D Pontoni Z Sapir; S Yefet; S Sloutskin; B Ocko; H Reichert; M Deutsch

2011-12-31T23:59:59.000Z

288

Centrifuge Techniques and Apparatus for Transport Experiments in Porous Media  

SciTech Connect (OSTI)

This paper describes experimental approaches and apparatus that we have developed to study solute and colloid transport in porous media using Idaho National Laboratory's 2-m radius centrifuge. The ex-perimental techniques include water flux scaling with applied acceleration at the top of the column and sub-atmospheric pressure control at the column base, automation of data collection, and remote experimental con-trol over the internet. These apparatus include a constant displacement piston pump, a custom designed liquid fraction collector based on switching valve technology, and modified moisture monitoring equipment. Suc-cessful development of these experimental techniques and equipment is illustrated through application to transport of a conservative tracer through unsaturated sand column, with centrifugal acceleration up to 40 gs. Development of such experimental equipment that can withstand high accelerations enhances the centrifuge technique to conduct highly controlled unsaturated solute/colloid transport experiments and allows in-flight liquid sample collection of the effluent.

Earl D. Mattson; Carl D. Paler; Robert W. Smith; Markus Flury

2010-06-01T23:59:59.000Z

289

POROUS WALL, HOLLOW GLASS MICROSPHERES  

SciTech Connect (OSTI)

Hollow Glass Microspheres (HGM) is not a new technology. All one has to do is go to the internet and Google{trademark} HGM. Anyone can buy HGM and they have a wide variety of uses. HGM are usually between 1 to 100 microns in diameter, although their size can range from 100 nanometers to 5 millimeters in diameter. HGM are used as lightweight filler in composite materials such as syntactic foam and lightweight concrete. In 1968 a patent was issued to W. Beck of the 3M{trademark} Company for 'Glass Bubbles Prepared by Reheating Solid Glass Particles'. In 1983 P. Howell was issued a patent for 'Glass Bubbles of Increased Collapse Strength' and in 1988 H. Marshall was issued a patent for 'Glass Microbubbles'. Now Google{trademark}, Porous Wall, Hollow Glass Microspheres (PW-HGMs), the key words here are Porous Wall. Almost every article has its beginning with the research done at the Savannah River National Laboratory (SRNL). The Savannah River Site (SRS) where SRNL is located has a long and successful history of working with hydrogen and its isotopes for national security, energy, waste management and environmental remediation applications. This includes more than 30 years of experience developing, processing, and implementing special ceramics, including glasses for a variety of Department of Energy (DOE) missions. In the case of glasses, SRS and SRNL have been involved in both the science and engineering of vitreous or glass based systems. As a part of this glass experience and expertise, SRNL has developed a number of niches in the glass arena, one of which is the development of porous glass systems for a variety of applications. These porous glass systems include sol gel glasses, which include both xerogels and aerogels, as well as phase separated glass compositions, that can be subsequently treated to produce another unique type of porosity within the glass forms. The porous glasses can increase the surface area compared to 'normal glasses of a 1 to 2 order of magnitude, which can result in unique properties in areas such as hydrogen storage, gas transport, gas separations and purifications, sensors, global warming applications, new drug delivery systems and so on. One of the most interesting porous glass products that SRNL has developed and patented is Porous Wall, Hollow Glass Microspheres (PW-HGMs) that are being studied for many different applications. The European Patent Office (EPO) just recently notified SRS that the continuation-in-part patent application for the PW-HGMs has been accepted. The original patent, which was granted by the EPO on June 2, 2010, was validated in France, Germany and the United Kingdom. The microspheres produced are generally in the range of 2 to 100 microns, with a 1 to 2 micron wall. What makes the SRNL microspheres unique from all others is that the team in Figure 1 has found a way to induce and control porosity through the thin walls on a scale of 100 to 3000 {angstrom}. This is what makes the SRNL HW-HGMs one-of-a-kind, and is responsible for many of their unique properties and potential for various applications, including those in tritium storage, gas separations, H-storage for vehicles, and even a variety of new medical applications in the areas of drug delivery and MRI contrast agents. SRNL Hollow Glass Microspheres, and subsequent, Porous Wall, Hollow Glass Microspheres are fabricated using a flame former apparatus. Figure 2 is a schematic of the apparatus.

Sexton, W.

2012-06-30T23:59:59.000Z

290

Metal recovery from porous materials  

DOE Patents [OSTI]

A method is described for recovering plutonium and other metals from materials by leaching comprising the steps of incinerating the materials to form a porous matrix as the residue of incineration, immersing the matrix into acid in a microwave-transparent pressure vessel, sealing the pressure vessel, and applying microwaves so that the temperature and the pressure in the pressure vessel increase. The acid for recovering plutonium can be a mixture of HBF[sub 4] and HNO[sub 3] and preferably the pressure is increased to at least 100 PSI and the temperature to at least 200 C. The porous material can be pulverized before immersion to further increase the leach rate.

Sturcken, E.F.

1992-10-13T23:59:59.000Z

291

Activation of porous MOF materials  

DOE Patents [OSTI]

A method for the treatment of solvent-containing MOF material to increase its internal surface area involves introducing a liquid into the MOF in which liquid the solvent is miscible, subjecting the MOF to supercritical conditions for a time to form supercritical fluid, and releasing the supercritical conditions to remove the supercritcal fluid from the MOF. Prior to introducing the liquid into the MOF, occluded reaction solvent, such as DEF or DMF, in the MOF can be exchanged for the miscible solvent.

Hupp, Joseph T; Farha, Omar K

2014-04-01T23:59:59.000Z

292

Activation of porous MOF materials  

DOE Patents [OSTI]

A method for the treatment of solvent-containing MOF material to increase its internal surface area involves introducing a liquid into the MOF in which liquid the solvent is miscible, subjecting the MOF to supercritical conditions for a time to form supercritical fluid, and releasing the supercritical conditions to remove the supercritical fluid from the MOF. Prior to introducing the liquid into the MOF, occluded reaction solvent, such as DEF or DMF, in the MOF can be exchanged for the miscible solvent.

Hupp, Joseph T; Farha, Omar K

2013-04-23T23:59:59.000Z

293

Gas sensor incorporating a porous framework  

DOE Patents [OSTI]

The disclosure provides sensor for gas sensing including CO.sub.2 gas sensors comprising a porous framework sensing area for binding an analyte gas.

Yaghi, Omar M; Czaja, Alexander U; Wang, Bo; Galatsis, Kosmas; Wang, Kang L; Furukawa, Hiroyasu

2014-05-27T23:59:59.000Z

294

Gas sensor incorporating a porous framework  

SciTech Connect (OSTI)

The disclosure provides sensor for gas sensing including CO.sub.2 gas sensors comprising a porous framework sensing area for binding an analyte gas.

Yaghi, Omar M.; Czaja, Alexander U.; Wang, Bo; Furukawa, Hiroyasu; Galatsis, Kosmas; Wang, Kang L.

2013-07-09T23:59:59.000Z

295

Alteration of gas phase ion polarizabilities upon hydration in high dielectric liquids  

E-Print Network [OSTI]

We investigate the modification of gas phase ion polarizabilities upon solvation in polar solvents and ionic liquids. To this aim, we develop a classical electrostatic theory of charged liquids composed of solvent molecules modeled as finite size dipoles, and embedding polarizable ions that consist of Drude oscillators. In qualitative agreement with ab-initio calculations of polar solvents and ionic liquids, the hydration energy of a polarizable ion in both type of dielectric liquid is shown to favor the expansion of its electronic cloud. Namely, the ion carrying no dipole moment in the gas phase acquires a dipole moment in the liquid environment, but its electron cloud also reaches an enhanced rigidity. We find that the overall effect is an increase of the gas phase polarizability upon hydration. In the specific case of ionic liquids, it is shown that this hydration process is driven by a collective solvation mechanism where the dipole moment of a polarizable ion induced by its interaction with surrounding ions self-consistently adds to the polarization of the liquid, thereby amplifying the dielectric permittivity of the medium in a substantial way. We propose this self-consistent hydration as the underlying mechanism behind the high dielectric permittivities of ionic liquids composed of small charges with negligible gas phase dipole moment. Hydration being a correlation effect, the emerging picture indicates that electrostatic correlations cannot be neglected in polarizable liquids.

Sahin Buyukdagli; Tapio Ala-Nissila

2013-04-23T23:59:59.000Z

296

Infrared Spectroscopy and Optical Constants of Porous Amorphous...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Spectroscopy and Optical Constants of Porous Amorphous Solid Water. Infrared Spectroscopy and Optical Constants of Porous Amorphous Solid Water. Abstract: Reflection-absorption...

297

Determination of Water Saturation in Relatively Dry Porous Media...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Water Saturation in Relatively Dry Porous Media Using Gas-phase Tracer Tests. Determination of Water Saturation in Relatively Dry Porous Media Using Gas-phase Tracer Tests....

298

Removal of Carbon Tetrachloride from a Layered Porous Medium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Carbon Tetrachloride from a Layered Porous Medium by Means of Soil Vapor Extraction Enhanced by Desiccation and Water Removal of Carbon Tetrachloride from a Layered Porous Medium...

299

Removal of carbon tetrachloride from a layered porous medium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

carbon tetrachloride from a layered porous medium by means of soil vapor extraction enhanced by desiccation and water Removal of carbon tetrachloride from a layered porous medium...

300

Hierarchically Porous Graphene as a Lithium-Air Battery Electrode...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Hierarchically Porous Graphene as a Lithium-Air Battery Electrode. Hierarchically Porous Graphene as a Lithium-Air Battery Electrode. Abstract: Functionalized graphene sheets (FGS)...

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

ZnO/porous-Si and TiO{sub 2}/porous-Si nanocomposite nanopillars  

SciTech Connect (OSTI)

Porous Si nanopillar arrays are used as templates for atomic layer deposition of ZnO and TiO{sub 2}, and thus, ZnO/porous-Si and TiO{sub 2}/porous-Si nanocomposite nanopillars are fabricated. The diffusion of the precursor molecules into the inside of the porous structure occurs via Knudsen diffusion and is strongly limited by the small pore size. The luminescence of the ZnO/porous-Si nanocomposite nanopillars is also investigated, and the optical emission can be changed and even quenched after a strong plasma treatment. Such nanocomposite nanopillars are interesting for photocatalysis and sensors.

Wang, Dong, E-mail: dong.wang@tu-ilmenau.de; Yan, Yong; Schaaf, Peter [Chair Materials for Electronics, Institute of Materials Engineering and Institute of Micro- and Nanotechnologies MacroNano, TU Ilmenau, Gustav-Kirchhoff-Str. 5, 98693 Ilmenau (Germany); Sharp, Thomas [Oxford Instruments Plasma Technology Ltd., Yatton, Bristol BS49 4AP (United Kingdom); Schönherr, Sven; Ronning, Carsten [Institute for Solid State Physics, Friedrich Schiller University Jena, Max-Wien-Platz 1, 07743 Jena (Germany); Ji, Ran [SUSS MicroTec Lithography GmbH, Schleissheimer Str. 90, 85748 Garching (Germany)

2015-01-01T23:59:59.000Z

302

Integrated experimental and modeling study of the ionic conductivity...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

modeling study of the ionic conductivity of samaria-doped ceria thin films. Abstract: Oxygen diffusion and ionic conductivity of samaria-doped ceria (SDC) thin films have been...

303

Microelectromechanical pump utilizing porous silicon  

DOE Patents [OSTI]

A microelectromechanical (MEM) pump is disclosed which includes a porous silicon region sandwiched between an inlet chamber and an outlet chamber. The porous silicon region is formed in a silicon substrate and contains a number of pores extending between the inlet and outlet chambers, with each pore having a cross-section dimension about equal to or smaller than a mean free path of a gas being pumped. A thermal gradient is provided along the length of each pore by a heat source which can be an electrical resistance heater or an integrated circuit (IC). A channel can be formed through the silicon substrate so that inlet and outlet ports can be formed on the same side of the substrate, or so that multiple MEM pumps can be connected in series to form a multi-stage MEM pump. The MEM pump has applications for use in gas-phase MEM chemical analysis systems, and can also be used for passive cooling of ICs.

Lantz, Jeffrey W. (Albuquerque, NM); Stalford, Harold L. (Norman, OK)

2011-07-19T23:59:59.000Z

304

Hyperfine Effects in Ionic Orbital Electron Capture  

E-Print Network [OSTI]

The K-orbital electron capture in ions with one or two electrons is analized for a general allowed nuclear transition. For ionic hyperfine states the angular neutrino distribution and the electron capture rate are given in terms of nuclear matrix elements. A possible application towards the determination of neutrino parameters is outlined.

M. A. Goñi

2010-03-02T23:59:59.000Z

305

Catalyst for hydrotreating carbonaceous liquids  

DOE Patents [OSTI]

A catalyst for denitrogenating and desulfurating carbonaceous liquid such as solvent refined coal includes catalytic metal oxides impregnated within a porous base of mostly alumina with relatively large pore diameters, surface area and pore volume. The base material includes pore volumes of 0.7-0.85 ml/g, surface areas of 200-350 m.sup.2 /g and pore diameters of 85-200 Angstroms. The catalytic metals impregnated into these base materials include the oxides of Group VI metals, molybdenum and tungsten, and the oxides of Group VIII metals, nickel and cobalt, in various combinations. These catalysts and bases in combination have effectively promoted the removal of chemically combined sulfur and nitrogen within a continuous flowing mixture of carbonaceous liquid and hydrogen gas.

Berg, Lloyd (Bozeman, MT); McCandless, Frank P. (Bozeman, MT); Ramer, Ronald J. (Idaho Falls, ID)

1982-01-01T23:59:59.000Z

306

Winter Performance and Maintenance of Porous Asphalt Pavements  

E-Print Network [OSTI]

Concrete (HSG-B)Porous Asphalt (HSG-C) #12;Cold Climate Performance Results #12;12 Porous Asphalt SurfaceWinter Performance and Maintenance of Porous Asphalt Pavements Robert M. Roseen, Ph.D., P.E., D impacts for new development and reverse impacts in areas with redevelopment. #12;Porous Asphalt Design

307

Porous Pavement in Cold Climates Part: Performance and Cost  

E-Print Network [OSTI]

90 80 70 60 50 40 30 20 10 0 %RemovalEfficiency Porous Asphalt Pervious Concrete Retention Pond ` #12;17 Hydrrologic Performance of Porous Pavements Pervious Concrete (HSG-B)Porous Asphalt (HSG-C) #12;0 10 20 30 40Porous Pavement in Cold Climates Part: Performance and Cost Onondaga Environmental Institute 17

308

Diffuse charge and Faradaic reactions in porous electrodes  

E-Print Network [OSTI]

Porous electrodes instead of flat electrodes are widely used in electrochemical systems to boost storage

Biesheuvel, P. M.

309

Forced dewetting on porous media  

E-Print Network [OSTI]

We study the dewetting of a porous plate withdrawn from a bath of fluid. The microscopic contact angle is fixed to zero and the flow is assumed to be parallel to the plate (lubrication approximation). The ordinary differential equation involving the position of the water surface is analysed in phase space by means of numerical integration. We show the existence of a critical value of the capillary number $\\eta U / \\gamma$, above which no stationary contact line can exist. An analytical model, based on asymptotic matching is developed, that reproduces the dependence of the critical capillary number on the angle of the plate with respect to the horizontal for large control parameters (3/2 power law).

Olivier Devauchelle; Christophe Josserand; Stephane Zaleski

2005-09-13T23:59:59.000Z

310

Multiphase flow in fractured porous media  

SciTech Connect (OSTI)

The major goal of this research project was to improve the understanding of the gas-oil two-phase flow in fractured porous media. In addition, miscible displacement was studied to evaluate its promise for enhanced recovery.

Firoozabadi, A.

1995-02-01T23:59:59.000Z

311

Anomalous transport through porous and fractured media  

E-Print Network [OSTI]

Anomalous transport, understood as the nonlinear scaling with time of the mean square displacement of transported particles, is observed in many physical processes, including contaminant transport through porous and fractured ...

Kang, Peter Kyungchul

2014-01-01T23:59:59.000Z

312

Modelling and characterisation of porous materials.  

E-Print Network [OSTI]

??Porous materials possessing random microstructures exist in both organic (e.g. polymer foam, bone) and in-organic (e.g. silica aerogels) forms. Foams and aerogels are two such… (more)

Alsayednoor, Jafar

2013-01-01T23:59:59.000Z

313

Characterization of naturally occurring porous media  

E-Print Network [OSTI]

characteristics of natural occur- ring porous media, The gR /K dimensionless ratio is related to the minimum water saturation in the reverse manner as is permeability. REFERENCES Wyllie, M. R. J. and M. B. Spangler: Application of Electrical Resistivity...: Resistivity of Brine-Saturated Sands in Relation to Pore Seometry. Cornell, D. snd D. L. Kstz: Flow of Sases through Consolidated Porous Media. Industrial and En ineeri hemietr (October 1953) Vo . 5, p. 21 5. Leverett, N, C. : Capillary Behavior...

Riley, Robert Daniel

1965-01-01T23:59:59.000Z

314

Method for preparing porous metal hydride compacts  

DOE Patents [OSTI]

A method for preparing porous metallic-matrix hydride compacts which can be repeatedly hydrided and dehydrided without disintegration. A mixture of a finely divided metal hydride and a finely divided matrix metal is contacted with a poison which prevents the metal hydride from dehydriding at room temperature and atmospheric pressure. The mixture of matrix metal and poisoned metal hydride is then compacted under pressure at room temperature to form porous metallic-matrix hydride compacts.

Ron, M.; Gruen, D.M.; Mendelsohn, M.H.; Sheft, I.

1980-01-21T23:59:59.000Z

315

Porous polymeric materials for hydrogen storage  

DOE Patents [OSTI]

A porous polymer, poly-9,9'-spirobifluorene and its derivatives for storage of H.sub.2 are prepared through a chemical synthesis method. The porous polymers have high specific surface area and narrow pore size distribution. Hydrogen uptake measurements conducted for these polymers determined a higher hydrogen storage capacity at the ambient temperature over that of the benchmark materials. The method of preparing such polymers, includes oxidatively activating solids by CO.sub.2/steam oxidation and supercritical water treatment.

Yu, Luping; Liu, Di-Jia; Yuan, Shengwen; Yang, Junbing

2013-04-02T23:59:59.000Z

316

Method for preparing porous metal hydride compacts  

DOE Patents [OSTI]

A method for preparing porous metallic-matrix hydride compacts which can be repeatedly hydrided and dehydrided without disintegration. A mixture of a finely divided metal hydride and a finely divided matrix metal is contacted with a poison which prevents the metal hydride from dehydriding at room temperature and atmospheric pressure. The mixture of matrix metal and poisoned metal hydride is then compacted under pressure at room temperature to form porous metallic-matrix hydride compacts.

Ron, Moshe (Haifa, IL); Gruen, Dieter M. (Downers Grove, IL); Mendelsohn, Marshall H. (Woodridge, IL); Sheft, Irving (Oak Park, IL)

1981-01-01T23:59:59.000Z

317

Asymmetric Framework for Predicting Liquid-Liquid Equilibrium of Ionic Liquid-Mixed Solvent Systems: II. Prediction of Ternary Systems  

E-Print Network [OSTI]

as to predictions obtained from standard symmetric models. Results indicate that an asymmetric NRTL/eNRTL model parameters are needed are the conventional (symmetric) NRTL, electrolyte-NRTL (eNRTL) and UNIQUAC models and the new asymmetric NRTL/eNRTL model. 2.1 Fully Adjustable Parameters For each of the models considered, we

Stadtherr, Mark A.

318

Neutral-ionic transitions in organic mixed-stack compounds  

SciTech Connect (OSTI)

Torrance et al. have made the interesting observation that several mixed-stack organic compounds undergo transitions from neutral states to ionic states as the temperature or pressure is varied. We examine a simple model of such transitions including Coulomb interaction and hybridization of neutral and ionic states. In the limit of weak hybridization and long-range repulsive interaction between ionic planes, it is proven that there is a complete devil's staircase where the degree of ionicity assumes an infinity of rational values. For attractive interactions between ionic planes, the neutral-ionic transition is shown to be first order for weak hybridization. Comparison with experiment indicates that this situation applies to tetrathiafulvalene (TTF) chloranil. For strong hybridization the transition is continuous but goes through a metallic phase. It is shown, for the first time, that the spectrum of the charge-transfer Hamiltonian contains both a bound spectrum, the observed charge-transfer excitations, and a continuum.

Bruinsma, R.; Bak, P.; Torrance, J.B.

1983-01-01T23:59:59.000Z

319

SRNL POROUS WALL GLASS MICROSPHERES  

SciTech Connect (OSTI)

The Savannah River National Laboratory (SRNL) has developed a new medium for storage of hydrogen and other gases. This involves fabrication of thin, Porous Walled, Hollow Glass Microspheres (PW-HGMs), with diameters generally in the range of 1 to several hundred microns. What is unique about the glass microballons is that porosity has been induced and controlled within the thin, one micron thick walls, on the scale of 10 to several thousand Angstroms. This porosity results in interesting properties including the ability to use these channels to fill the microballons with special absorbents and other materials, thus providing a contained environment even for reactive species. Gases can now enter the microspheres and be retained on the absorbents, resulting in solid-state and contained storage of even reactive species. Also, the porosity can be altered and controlled in various ways, and even used to filter mixed gas streams within a system. SRNL is involved in about a half dozen different programs involving these PW-HGMs and an overview of some of these activities and results emerging are presented.

Wicks, G; Leung Heung, L; Ray Schumacher, R

2008-04-15T23:59:59.000Z

320

Study of liquid retention in fixed-bed reactors with upward flow of gas and liquid  

SciTech Connect (OSTI)

A literature survey of the measurement techniques for the determination of liquid retention in cocurrent upward gas and liquid flow in fixed-bed reactors is presented. A number of these techniques were used in this work in columns of different diameters (Dc = 0.05 m, 0.10 m, and 0.15 m). Porous alumina particles of two different diameters (dp = 0.002 m and 0.0028 m) with both nonfoaming (water, cyclohexane, heptane, and propanol) and foaming liquids (kerosene, LCO, and diesel fuel) have been investigated. The gas used was either air or N[sub 2]. The methods investigated include volumetry, gravimetry, gammametry, and determination of residence-time distribution by tracer technique. A simple correlation for the prediction of total gas and liquid retention for bubble and pulsed flow is proposed and verified.

Yang, X.L.; Euzen, J.P. (Inst. Francais du Petrole, Vernaison (France)); Wild, G. (Lab. des Sciences du Genie Chimique, Nancy (France))

1993-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

Final Report for DE-FG02-93ER14376,Ionic Transport in Electrochemical Media  

SciTech Connect (OSTI)

This project was a molecular dynamics study of the relevant issues associated with the structure and transport of lithium in polymer electrolytes such as polyethylene oxide(PEO). In close collaboration with quantum chemist Larry Curtiss and neutron scatterers David Lee Price and Marie-Louise Saboungi at Argonne, we used molecular dynamics to study the local structure and dynamics and ion transport in the polymer. The studies elucidated the mechanism of Li transport in PEO, revealing that the rate limiting step is extremely sensitive to the magnitude of the torsion forces in the backbone of the polymer. Because the torsion forces are difficult to manipulate chemically, this makes it easier to understand why improving the conductivity of PEO based electrolytes has proven to be very difficult. We studied the transport properties of cations in ionic liquids as possible additives to polymer membranes for batteries and fuel cells and found preliminary indications that the transport is enhanced near phase separation in acid-ionic liquid mixtures.

J. W. Halley

2009-05-20T23:59:59.000Z

322

Identification of polar, ionic, and highly water soluble organic pollutants in untreated industrial wastewaters  

SciTech Connect (OSTI)

This paper presents a generic protocol for the determination of polar, ionic, and highly water soluble organic pollutants on untreated industrial wastewaters involving the use of two different solid-phase extraction (SPE) methodologies followed by liquid chromatography-mass spectrometry (LC-MS). Untreated industrial wastewaters might contain natural and synthetic dissolved organic compounds with total organic carbon (TOC) values varying between 100 and 3000 mg/L. All polar, ionic and highly water soluble compounds comprising more than 95% of the organic content and with major contribution to the total toxicity of the sample cannot be analyzed by conventional gas chromatography-mass spectrometry (GC-MS), and LC-MS is a good alternative. In this work two extraction procedures were used to obtain fractionated extracts of the nonionic polar compounds: a polymeric Isolute ENV + SPE cartridge for the preconcentration of anionic analytes and a sequential solid-phase extraction (SSPE) method percolating the samples first in octadecylsilica cartridge in series with the polymeric Lichrolut EN cartridge. Average recoveries ranging from 72% to 103% were obtained for a variety of 23 different analytes. Determination of nonionic pollutants was accomplished by reverse-phase liquid chromatography-atmospheric pressure chemical ionization-mass spectrometry (LC-APCI-MS), while anionic compounds were analyzed by ion pair chromatography-electrospray-mass spectrometry (IP-ESI-MS) and LC-ESI-MS. This protocol was applied to a pilot survey of textile and tannery wastewaters leading to the identification and quantification of 33 organic pollutants.

Castillo, M.; Alonso, M.C.; Riu, J.; Barcelo, D. [IIQAB-CSIC, Barcelona (Spain). Dept. of Environmental Chemistry] [IIQAB-CSIC, Barcelona (Spain). Dept. of Environmental Chemistry

1999-04-15T23:59:59.000Z

323

Sandia National Laboratories: solid-state ionics  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administration the1developmentturbineredox-activeNational Solar Thermal Testthermalstate ionics Joint

324

Ionic Power Systems Ltd | Open Energy Information  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia: Energy Resources Jump to:46 - 429 Throttled (bot load)InternationalRenewable Energy6.3091865°,Power IncIonic

325

Methods of forming and using porous structures for energy efficient separation of light gases by capillary condensation  

DOE Patents [OSTI]

The present invention relates to an improved method and apparatus for separating one or more condensable compounds from a mixture of two or more gases of differing volatilities by capillary fractionation in a membrane-type apparatus, and a method of forming porous structures therefor. More particularly, the invention includes methods of forming and using an apparatus consisting, at least in part, of a porous structure having capillary-type passages extending between a plurality of small openings on the first side and larger openings on a second side of the structure, the passages being adapted to permit a condensed liquid to flow therethrough substantially by capillary forces, whereby vapors from the mixture are condensed, at least in part, and substantially in and adjacent to the openings on the first side, and are caused to flow in a condensed liquid state, substantially in the absence of vapor, from the openings on the first side to the openings on the second side.

Calamur, Narasimhan (Lemont, IL); Carrera, Martin E. (Naperville, IL); Devlin, David J. (Los Alamos, NM); Archuleta, Tom (Espanola, NM)

2000-01-01T23:59:59.000Z

326

Fabrication and characterization of porous shape memory alloys  

E-Print Network [OSTI]

This work details an investigation into the production of porous shape memory alloys (SMAs) via hot isostatic press (HIP) from prealloyed powders. HIPing is one of three main methods for producing porous SMAs, the other two are conventional...

Penrod, Luke Edward

2004-09-30T23:59:59.000Z

327

Joining of porous silicon carbide bodies  

DOE Patents [OSTI]

A method of joining two porous bodies of silicon carbide is disclosed. It entails utilizing an aqueous slip of a similar silicon carbide as was used to form the porous bodies, including the sintering aids, and a binder to initially join the porous bodies together. Then the composite structure is subjected to cold isostatic pressing to form a joint having good handling strength. Then the composite structure is subjected to pressureless sintering to form the final strong bond. Optionally, after the sintering the structure is subjected to hot isostatic pressing to further improve the joint and densify the structure. The result is a composite structure in which the joint is almost indistinguishable from the silicon carbide pieces which it joins.

Bates, Carl H. (Worcester, MA); Couhig, John T. (Worcester, MA); Pelletier, Paul J. (Thompson, CT)

1990-05-01T23:59:59.000Z

328

Investigation of porous media structures using NMR restricted diffusion measurements  

E-Print Network [OSTI]

coefficient which produces a new description of molecule diffusion in porous media. Experimental Details Model porous media chosen for investigation are water saturated glass bead packs of different bead sizes from 50 to 300 microns. First the glass beads... is accessible with the aid of sufficiently developed analysis procedures, NMR techniques can be applied to porous structure analysis. For the hypothesis that water saturated in porous media consists of two phases: water removed from domain boundaries...

Miao, Peizhi

1993-01-01T23:59:59.000Z

329

Synthesis and characterization of hybrid materials based on 1-butyl-3-methylimidazolium tetrafluoroborate ionic liquid and Dawson-type tungstophosphate K{sub 7}[H{sub 4}PW{sub 18}O{sub 62}].18H{sub 2}O and K{sub 6}[P{sub 2}W{sub 18}O{sub 62}].13H{sub 2}O  

SciTech Connect (OSTI)

In this study, we synthesized hybrid materials using well-Dawson polyoxometalates (POMs), K{sub 7}[H{sub 4}PW{sub 18}O{sub 62}].18H{sub 2}O or K{sub 6}[P{sub 2}W{sub 18}O{sub 62}].13H{sub 2}O and a room temperature ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM][BF{sub 4}]). K, W, P and CHN elemental analysis showed that one mole of [H{sub 4}PW{sub 18}O{sub 62}]{sup 7-} reacts with 6 moles of BMIM{sup +} and one mole of [P{sub 2}W{sub 18}O{sub 62}]{sup 6-} reacts with 4 moles of BMIM{sup +} to form, respectively, K[BMIM]{sub 6}H{sub 4}PW{sub 18}O{sub 62} and K{sub 2}[BMIM]{sub 4}P{sub 2}W{sub 18}O{sub 62}. X-ray diffraction illustrated amorphous structure of the hybrid materials. FT-IR spectra showed the presence of both 1-butyl-3-methylimidazolium cation and the Dawson anion. TG analysis displayed a relative thermal stability of the hybrid materials compared to the parents Dawson POMs. Cyclic voltammetry showed that the reduction peak potentials of the Dawson anion in the hybrid materials shift towards negative values and the shift is more pronounced for K[BMIM]{sub 6}H{sub 4}PW{sub 18}O{sub 62} compared to K{sub 2}[BMIM]{sub 4}P{sub 2}W{sub 18}O{sub 62}. This was attributed to a decrease in the acidity of the Dawson POM anion in the hybrid material. -- Graphical abstract: Powder XRD patterns of (a) PW{sub 18}, (b) K[BMIM]{sub 6}H{sub 4}PW{sub 18}O{sub 62}, (c) P{sub 2}W{sub 18}, and (d) K{sub 2}[BMIM]{sub 4}P{sub 2}W{sub 18}O{sub 62}. Display Omitted Research highlights: {yields} 1-butyl-3-methylimidazolium tetrafluoroborate([BMIM][BF{sub 4}]) reacts with K{sub 7}[H{sub 4}PW{sub 18}O{sub 62}].18H{sub 2}O to form K[BMIM]{sub 6}H{sub 4}PW{sub 18}O{sub 62}. {yields} [BMIM][BF{sub 4}] reacts with K{sub 6}[P{sub 2}W{sub 18}O{sub 62}].13H{sub 2}O to form K{sub 2}[BMIM]{sub 4}P{sub 2}W{sub 18}O{sub 62}. {yields} K[BMIM]{sub 6}H{sub 4}PW{sub 18}O{sub 62} and K{sub 2}[BMIM]{sub 4}P{sub 2}W{sub 18}O{sub 62} displayed amorphous structures. {yields} K[BMIM]{sub 6}H{sub 4}PW{sub 18}O{sub 62} and K{sub 2}[BMIM]{sub 4}P{sub 2}W{sub 18}O{sub 62} illustrated low water content. {yields} K[BMIM]{sub 6}H{sub 4}PW{sub 18}O{sub 62} and K{sub 2}[BMIM]{sub 4}P{sub 2}W{sub 18}O{sub 62} showed improved thermal stability.

Ammam, Malika, E-mail: m78ammam@yahoo.f [Department of Metallurgy and Materials Engineering (MTM), K.U Leuven, Kasteelpark Arenberg 44, B-3001 Heverlee (Belgium); Fransaer, Jan [Department of Metallurgy and Materials Engineering (MTM), K.U Leuven, Kasteelpark Arenberg 44, B-3001 Heverlee (Belgium)

2011-04-15T23:59:59.000Z

330

Phytoremediation of Ionic and Methyl Mercury P  

SciTech Connect (OSTI)

Our long-term goal is to enable highly productive plant species to extract, resist, detoxify, and/or sequester toxic heavy metal pollutants as an environmentally friendly alternative to physical remediation methods. We have focused this phytoremediation research on soil and water-borne ionic and methylmercury. Mercury pollution is a serious world-wide problem affecting the health of human and wild-life populations. Methylmercury, produced by native bacteria at mercury-contaminated wetland sites, is a particularly serious problem due to its extreme toxicity and efficient biomagnification in the food chain. We engineered several plant species (e.g., Arabidopsis, tobacco, canola, yellow poplar, rice) to express the bacterial genes, merB and/or merA, under the control of plant regulatory sequences. These transgenic plants acquired remarkable properties for mercury remediation. (1) Transgenic plants expressing merB (organomercury lyase) extract methylmercury from their growth substrate and degrade it to less toxic ionic mercury. They grow on concentrations of methylmercury that kill normal plants and accumulate low levels of ionic mercury. (2) Transgenic plants expressing merA (mercuric ion reductase) extract and electrochemically reduce toxic, reactive ionic mercury to much less toxic and volatile metallic mercury. This metal transformation is driven by the powerful photosynthetic reducing capacity of higher plants that generates excess NADPH using solar energy. MerA plants grow vigorously on levels of ionic mercury that kill control plants. Plants expressing both merB and merA degrade high levels of methylmercury and volatilize metallic mercury. These properties were shown to be genetically stable for several generations in the two plant species examined. Our work demonstrates that native trees, shrubs, and grasses can be engineered to remediate the most abundant toxic mercury pollutants. Building on these data our working hypothesis for the next grant period is that transgenic plants expressing the bacterial merB and merA genes will (a) remove mercury from polluted soil and water and (b) prevent methylmercury from entering the food chain. Our specific aims center on understanding the mechanisms by which plants process the various forms of mercury and volatilize or transpire mercury vapor. This information will allow us to improve the design of our current phytoremediation strategies. As an alternative to volatilizing mercury, we are using several new genes to construct plants that will hyperaccumulate mercury in above-ground tissues for later harvest. The Department of Energy's Oak Ridge National Laboratory and Brookhaven National Laboratory have sites with significant levels of mercury contamination that could be cleaned by applying the scientific discoveries and new phytoremediation technologies described in this proposal. The knowledge and expertise gained by engineering plants to hyperaccumulate mercury can be applied to the remediation of other heavy metals pollutants (e.g., arsenic, cesium, cadmium, chromium, lead, strontium, technetium, uranium) found at several DOE facilities.

Meagher, Richard B.

1999-06-01T23:59:59.000Z

331

Mechanical Properties of Porous-Matrix Ceramic Composites**  

E-Print Network [OSTI]

REVIEWS Mechanical Properties of Porous- Matrix Ceramic Composites** By Frank W. Zok* and Carlos G/Mechanical Properties of Porous-Matrix Ceramic Composites REVIEWS The porous matrix concept has been developed primarily. Levi 1. Introduction Damage tolerance can be enabled in continuous fiber-rein- forced ceramic

Zok, Frank

332

Porous polymeric materials for hydrogen storage  

DOE Patents [OSTI]

Porous polymers, tribenzohexazatriphenylene, poly-9,9'-spirobifluorene, poly-tetraphenyl methane and their derivatives for storage of H.sub.2 prepared through a chemical synthesis method. The porous polymers have high specific surface area and narrow pore size distribution. Hydrogen uptake measurements conducted for these polymers determined a higher hydrogen storage capacity at the ambient temperature over that of the benchmark materials. The method of preparing such polymers, includes oxidatively activating solids by CO.sub.2/steam oxidation and supercritical water treatment.

Yu, Luping (Hoffman Estates, IL); Liu, Di-Jia (Naperville, IL); Yuan, Shengwen (Chicago, IL); Yang, Junbing (Westmont, IL)

2011-12-13T23:59:59.000Z

333

Propagation of polymer slugs through porous media  

SciTech Connect (OSTI)

This paper describes an experimental and theoretical study of the mechanisms governing polymer slug propagation through porous media. An analytical model taking into account the macromolecule exclusion from pore walls is proposed to predict rodlike polymer velocity in porous media and thus the spreading out of polydispersed polymer slugs. Under conditions where this wall exclusion is maximum, i.e. at low shear rates and polymer concentrations, the experiments show that xanthan propagation is effectively predicted by this model. At higher flow rates and polymer concentrations, the effects of hydrodynamic dispersion and viscous fingering are analyzed. A new fractionation method for determining molecular weight distribution of polymers used in EOR is proposed.

Lecourtier, J.; Chauveteau, G.

1984-09-01T23:59:59.000Z

334

A model for reactive porous transport during re-wetting of hardened concrete  

E-Print Network [OSTI]

We develop a mathematical model that captures the transport of liquid water in hardened concrete, as well as the chemical reactions that occur between the infiltrating water and the residual calcium silicate compounds that reside in the porous concrete matrix. We investigate the hypothesis that the reaction product -- calcium silicate hydrate gel -- clogs the pores within the concrete thereby hindering water transport. Using numerical simulations, we determine the sensitivity of the model solution to changes in various physical parameters, and compare to experimental results available in the literature.

Chapwanya, Michael; Stockie, John M

2008-01-01T23:59:59.000Z

335

Porous ceramics and method for making  

SciTech Connect (OSTI)

The fabrication of a porous ceramic composite is described. Fumed silica particles are coated with a nitrate, preferably aluminum nitrate. Next the nitrate is converted to an oxide and formed into a desired configuration. This configuration is heated to convert the oxide to an oxide silicate which is then react with HF, resulting in the fluoride ceramic, preferably aluminum fluoride.

Reiner, R.H.; Holcombe, C.E.

1989-06-08T23:59:59.000Z

336

Method of making porous ceramic fluoride  

SciTech Connect (OSTI)

A process is disclosed for making a porous ceramic composite where fumed silica particles are coated with a nitrate, preferably aluminum nitrate. Next the nitrate is converted to an oxide and formed into a desired configuration. This configuration is heated to convert the oxide to an oxide silicate which is then react with HF, resulting in the fluoride ceramic, preferably aluminum fluoride.

Reiner, R.H.; Holcombe, C.E.

1990-11-13T23:59:59.000Z

337

Porous radiant burners having increased radiant output  

DOE Patents [OSTI]

Means and methods for enhancing the output of radiant energy from a porous radiant burner by minimizing the scattering and increasing the adsorption, and thus emission of such energy by the use of randomly dispersed ceramic fibers of sub-micron diameter in the fabrication of ceramic fiber matrix burners and for use therein.

Tong, Timothy W. (Tempe, AZ); Sathe, Sanjeev B. (Tempe, AZ); Peck, Robert E. (Tempe, AZ)

1990-01-01T23:59:59.000Z

338

Method of making porous ceramic fluoride  

DOE Patents [OSTI]

A process for making a porous ceramic composite where fumed silica particles are coated with a nitrate, preferably aluminum nitrate. Next the nitrate is converted to an oxide and formed into a desired configuration. This configuration is heated to convert the oxide to an oxide silicate which is then react with HF, resulting in the fluoride ceramic, preferably aluminum fluoride.

Reiner, Robert H. (Knoxville, TN); Holcombe, Cressie E. (Farragut, TN)

1990-01-01T23:59:59.000Z

339

Structural simulations of nanomaterials self-assembled from ionic macrocycles.  

SciTech Connect (OSTI)

Recent research at Sandia has discovered a new class of organic binary ionic solids with tunable optical, electronic, and photochemical properties. These nanomaterials, consisting of a novel class of organic binary ionic solids, are currently being developed at Sandia for applications in batteries, supercapacitors, and solar energy technologies. They are composed of self-assembled oligomeric arrays of very large anions and large cations, but their crucial internal arrangement is thus far unknown. This report describes (a) the development of a relevant model of nonconvex particles decorated with ions interacting through short-ranged Yukawa potentials, and (b) the results of initial Monte Carlo simulations of the self-assembly binary ionic solids.

van Swol, Frank B.; Medforth, Craig John (University of New Mexico, Albuquerque, NM)

2010-10-01T23:59:59.000Z

340

Decoupling of Ionic Trasport from Segmental Relaxation in Polymer Electrolytes  

SciTech Connect (OSTI)

We present detailed studies of the relationship between ionic conductivity and segmental relaxation in polymer electrolytes. The analysis shows that the ionic conductivity can be decoupled from segmental dynamics and the strength of the decoupling correlates with the fragility but not with the glass transition temperature. These results call for a revision of the current picture of ionic transport in polymer electrolytes. We relate the observed decoupling phenomenon to frustration in packing of rigid polymers, where the loose local structure is also responsible for the increase in their fragility.

Wang, Yangyang [ORNL; Agapov, Alexander L [ORNL; Fan, Fei [ORNL; Hong, Kunlun [ORNL; Yu, Xiang [ORNL; Mays, Jimmy [ORNL; Sokolov, Alexei P [ORNL

2012-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

Screening model for nanowire surface-charge sensors in liquid  

E-Print Network [OSTI]

The conductance change of nanowire field-effect transistors is considered a highly sensitive probe for surface charge. However, Debye screening of relevant physiological liquid environments challenge device performance due to competing screening from the ionic liquid and nanowire charge carriers. We discuss this effect within Thomas-Fermi and Debye-Huckel theory and derive analytical results for cylindrical wires which can be used to estimate the sensitivity of nanowire surface-charge sensors. We study the interplay between the nanowire radius, the Thomas-Fermi and Debye screening lengths, and the length of the functionalization molecules. The analytical results are compared to finite-element calculations on a realistic geometry.

Martin H. Sorensen; Niels Asger Mortensen; Mads Brandbyge

2007-08-17T23:59:59.000Z

342

Process for the production of liquid hydrocarbons  

DOE Patents [OSTI]

The present invention concerns a process for the preparation of liquid hydrocarbons which process comprises contacting synthesis gas with a slurry of solid catalyst particles and a liquid in a reactor vessel by introducing the synthesis gas at a low level into the slurry at conditions suitable for conversion of the synthesis gas into liquid hydrocarbons, the solid catalyst particles comprising a catalytic active metal selected from cobalt or iron on a porous refractory oxide carrier, preferably selected from silica, alumina, titania, zirconia or mixtures thereof, the catalyst being present in an amount between 10 and 40 vol. percent based on total slurry volume liquids and solids, and separating liquid material from the solid catalyst particles by using a filtration system comprising an asymmetric filtration medium (the selective side at the slurry side), in which filtration system the average pressure differential over the filtration medium is at least 0.1 bar, in which process the particle size distribution is such that at least a certain amount of the catalyst particles is smaller than the average pore size of the selective layer of the filtration medium. The invention also comprises an apparatus to carry out the process described above.

Bhatt, Bharat Lajjaram; Engel, Dirk Coenraad; Heydorn, Edward Clyde; Senden, Matthijis Maria

2006-06-27T23:59:59.000Z

343

Experimental Investigation of the Effective Foam Viscosity in Unsaturated Porous Media  

SciTech Connect (OSTI)

Foam has the potential to effectively carry and distribute either aqueous or gaseous amendments to the deep vadose zone for contaminant remediation. However, the transport of foam in porous media is complicated because flow characteristics such as the effective viscosity are affected not only by foam properties but also by the sediment properties and flow conditions. We determined the average effective foam viscosity via a series of laboratory experiments and found that the effective foam viscosity increased with the liquid fraction in foam, the injection rate, and sediment permeability. These impacts are quantified with an empirical expression, which is further demonstrated with data from literature. The results show that the liquid fraction in foam and sediment permeability are two primary factors affecting effective foam viscosity. These results suggest that, when foam is used in deep vadose zone remediation, foam flow will not suffer from gravitational drainage and can distribute amendments uniformly in heterogeneous sediments.

Zhang, Z. F.; Zhong, Lirong; White, Mark D.; Szecsody, James E.

2012-11-01T23:59:59.000Z

344

Tunable ionic-conductivity of collapsed Sandia octahedral molecular sieves (SOMS).  

SciTech Connect (OSTI)

This proposal focuses on the synthesis and characterization of ''tunable'' perovskite ceramics with resulting controlled strength and temperature of dielectric constants and/or with ionic conductivity. Traditional methods of synthesis involve high temperature oxide mixing and baking. We developed a new methodology of synthesis involving the (1) low temperature hydrothermal synthesis of metastable porous phases with ''tuned'' stoichiometry, and element types, and then (2) low temperature heat treatment to build exact stoichiometry perovskites, with the desired vacancy concentrations. This flexible pathway can lead to compositions and structures not attainable by conventional methods. During the course of this program, a series of Na-Nb perovskites were synthesized by calcining and collapsing microporous Sandia Octahedral Molecular Sieve (SOMS) phases. These materials were studied by various characterization techniques and conductivity measurements to better delineate stability and stoichiometry/bulk conductivity relationships. The conductivity can be altered by changing the concentration and type of the substituting framework cation(s) or by ion exchange of sodium. To date, the Na{sub 0.9}Mg{sub 0.1}Nb{sub 0.8}Ti{sub 0.2}O{sub 3-{delta}} shows the best conductivity.

Pless, Jason; Nenoff, Tina Maria; Garino, Terry J.; Axness, Marlene

2006-11-01T23:59:59.000Z

345

Dynamics of DNAPL penetration into fractured porous media  

SciTech Connect (OSTI)

Dense nonaqueous phase liquids (DNAPLs) that pool above stratigraphic contacts as a result of capillary forces can migrate downward through fractures in the underlying fine-grained layer. Although the DNAPL in the fracture is excluded from the surrounding porous matrix by capillary forces, the DNAPL constituent will dissolve and migrate by diffusion into the matrix. As a front of moderately soluble DNAPL advances into a fracture, the flux of dissolved material into the matrix increases until it becomes comparable to the rate of flow into the fracture, reducing the pressure in the DNAPL phase and slowing its advance. If the DNAPL front encounters a constriction with sufficiently large entry pressure, its advance will halt temporarily. But as the concentration gradients driving diffusion into the matrix decrease, there will be less DNAPL lost by diffusion and the DNAPL pressure at the constriction will increase until it exceeds the entry pressure, causing the downward advance of the front to suddenly resume. Because the time scales of diffusion are much slower than those of density flow, this analysis suggests that under certain circumstances a DNAPL can suddenly resume its downward advance after a long period of apparent immobility. In one plausible example, a dichloromethane front passes through 5 m of fractured clay in 16 days, is immobile for more than four years, and then suddenly moves again. Where this phenomenon is possible, removal of DNAPL to protect underlying aquifers becomes more important as a remediation goal.

Ross, B. [Disposal Safety Inc., Washington, DC (United States); Lu, N. [Colorado School of Mines, Golden, CO (United States). Div. of Engineering

1999-01-01T23:59:59.000Z

346

Electric Double-Layer Capacitor Based on an Ionic Clathrate Hydrate  

SciTech Connect (OSTI)

Herein, we suggest a new approach to an electric double-layer capacitor (EDLC) that is based on a proton-conducting ionic clathrate hydrate (ICH). The ice-like structures of clathrate hydrates, which are comprised of host water molecules and guest ions, make them suitable for applications in EDLC electrolytes, owing to their high proton conductivities and thermal stabilities. The carbon materials in the ICH Me{sub 4}NOH[DOT OPERATOR]5?H{sub 2}O show a high specific capacitance, reversible charge–discharge behavior, and a long cycle life. The ionic-hydrate complex provides the following advantages in comparison with conventional aqueous and polymer electrolytes: 1)?The ICH does not cause leakage problems under normal EDLC operating conditions. 2)?The hydrate material can be utilized itself, without requiring any pre-treatments or activation for proton conduction, thus shortening the preparation procedure of the EDLC. 3)?The crystallization of the ICH makes it possible to tailor practical EDLC dimensions because of its fluidity as a liquid hydrate. 4)?The hydrate solid electrolyte exhibits more-favorable electrochemical stability than aqueous and polymer electrolytes. Therefore, ICH materials are expected to find practical applications in versatile energy devices that incorporate electrochemical systems.

Lee, Wonhee; Kwon, Minchul; Park, Seongmin; Lim, Dongwook Cha, Dr Jong-Ho; Lee, Dr. Huen

2013-07-01T23:59:59.000Z

347

THIN LIQUID WALL BEHAVIOR UNDER IFE CYCLIC OPERATION A. R. Raffray  

E-Print Network [OSTI]

to the requirements imposed by the driver and target thermal and injection control. I. INTRODUCTION A wetted wall relative to the requirements imposed by the driver and target thermal and injection control. In determining of thin liquid film protection systems with either radial injection through a porous first wall (hereafter

Najmabadi, Farrokh

348

Plasmas in Multiphase Media: Bubble Enhanced Discharges in Liquids and Plasma/Liquid Phase Boundaries  

SciTech Connect (OSTI)

In this research project, the interaction of atmospheric pressure plasmas with multi-phase media was computationally investigated. Multi-phase media includes liquids, particles, complex materials and porous surfaces. Although this investigation addressed fundamental plasma transport and chemical processes, the outcomes directly and beneficially affected applications including biotechnology, medicine and environmental remediation (e.g., water purification). During this project, we made advances in our understanding of the interaction of atmospheric pressure plasmas in the form of dielectric barrier discharges and plasma jets with organic materials and liquids. We also made advances in our ability to use computer modeling to represent these complex processes. We determined the method that atmospheric pressure plasmas flow along solid and liquid surfaces, and through endoscopic like tubes, deliver optical and high energy ion activation energy to organic and liquid surfaces, and produce reactivity in thin liquid layers, as might cover a wound. We determined the mechanisms whereby plasmas can deliver activation energy to the inside of liquids by sustaining plasmas in bubbles. These findings are important to the advancement of new technology areas such as plasma medicine

Kushner, Mark Jay [University of Michigan] [University of Michigan

2014-07-10T23:59:59.000Z

349

Effects of pH and ionic strength on sulfamethoxazole and ciprofloxacin transport in saturated porous media  

E-Print Network [OSTI]

: Antibiotics Mobility Sand column Solution chemistry Modeling 1. Introduction In the past decade, there has antibiotics regarded as emerging contaminants have been frequently detected in soils and groundwater; however.6, but still no CIP was detected in the effluents. A mathematical model based on advection­dispersion equation

Ma, Lena

350

Electronically and ionically conducting electrodes for thermoelectric generators  

DOE Patents [OSTI]

A composite article comprising a porous cermet electrode on a dense solid electrolyte and method of making same. The cerment electrode comprises beta-type-alumina and refractory metal.

Novak, Robert F. (Farmington Hills, MI); Weber, Neill (Murray, UT)

1987-01-01T23:59:59.000Z

351

Liquid electrode  

DOE Patents [OSTI]

A dropping electrolyte electrode is described for use in electrochemical analysis of non-polar sample solutions, such as benzene or cyclohexane. The liquid electrode, preferably an aqueous salt solution immiscible in the sample solution, is introduced into the solution in dropwise fashion from a capillary. The electrolyte is introduced at a known rate, thus, the droplets each have the same volume and surface area. The electrode is used in making standard electrochemical measurements in order to determine properties of non-polar sample solutions. 2 figures.

Ekechukwu, A.A.

1994-07-05T23:59:59.000Z

352

Heat transfer enhancement in a channel with porous baffles  

E-Print Network [OSTI]

with staggered positioned porous baffles. A numerical procedure was implemented, in conjunction with a commercially available Navier-Stokes solver, to model the turbulent flow in porous media. The Brinkman-Forchheimer-Extended Darcy model was used for modeling... fluid flow through the porous baffles. Conventional, one- equation, and two-equation models were used for heat transfer modeling. The accuracy and characteristics of each model were investigated and discussed. The results were compared...

Ko, Kang-Hoon

2005-02-17T23:59:59.000Z

353

Desiccation of unsaturated porous media: Intermediate-scale experiment...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

with the multifluid flow simulator STOMP, using independently obtained hydraulic and thermal porous medium properties. In all the experiments, the injection of dry air proved...

354

Living Bacterial Sacrificial Porogens to Engineer Decellularized Porous Scaffolds  

E-Print Network [OSTI]

Decellularization and cellularization of organs have emerged as disruptive methods in tissue engineering and regenerative medicine. Porous hydrogel scaffolds have widespread applications in tissue engineering, regenerative ...

Xu, Feng

355

multiscale flow and transport in porous media - Department of ...  

E-Print Network [OSTI]

Multiphase ow and transport in heterogeneous porous media is typically ... we discuss two model problems: contaminant transport in aquifers and water ooding

356

Transport in Porous Media ISSN 0169-3913  

E-Print Network [OSTI]

-011-9720-2 Applicability of the Linearized Governing Equation of Gas Flow in Porous Media Jian Li · Hongbin Zhan · Guanhua

Zhan, Hongbin

357

Fast, Low Cost Method for Manufacturing Porous Structures for...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Advanced Materials Advanced Materials Find More Like This Return to Search Fast, Low Cost Method for Manufacturing Porous Structures for Fuel Cells, Catalysts and Filtration...

358

Etch-free Formation of Porous Silicon by High-energy Ion Irradiation...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Etch-free Formation of Porous Silicon by High-energy Ion Irradiation. Etch-free Formation of Porous Silicon by High-energy Ion Irradiation. Abstract: In this study, porous silicon...

359

Low-Cost, Haziness-Free, Transparent Insulation Based On a Porous...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Low-Cost, Haziness-Free, Transparent Insulation Based On a Porous Silica Material Low-Cost, Haziness-Free, Transparent Insulation Based On a Porous Silica Material Image of porous...

360

Porous, sintered metal filter recovers 100% of catalyst in H/sub 2/O/sub 2/ process  

SciTech Connect (OSTI)

Recovery of catalyst and prevention of catalyst from entering the oxidizer were plant problems for the Interox America process for production of H/sub 2/O/sub 2/ by the catalyzed alternative hydrogenation and oxidation of anthraquinone. A porous metal filter element was inserted in the filter unit following the hydrogenation stage to collect the catalyst which forms a permeable cake that is recovered by backwashing on a timer cycle. The porous metal filters consisting of a rigid matrix containing small pores applicable for the collection of very small particles (> 0.5 ..mu.. in liquids and 0.05 ..mu.. in gases) have been in use in plants in UK for 25 years with 75% of the original filter elements still in use. (BLM)

Hall, G.L.; Isaacs, M.

1982-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

In Situ One-Step Synthesis of Hierarchical Nitrogen-Doped Porous...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Synthesis of Hierarchical Nitrogen-Doped Porous Carbon for High Performance Supercapacitors. In Situ One-Step Synthesis of Hierarchical Nitrogen-Doped Porous Carbon for High...

362

High-throughput Characterization of Porous Materials Using Graphics Processing Units  

E-Print Network [OSTI]

A.E. ; Purcell, T. Computer Graphics Forum 2007, 26(1), 80-of Porous Materials Using Graphics Processing Units Jihanof Porous Materials Using Graphics Processing Units Jihan

Kim, Jihan

2013-01-01T23:59:59.000Z

363

Liquid foams of graphene  

E-Print Network [OSTI]

Liquid foams are dispersions of bubbles in a liquid. Bubbles are stabilized by foaming agents that position at the interface between the gas and the liquid. Most foaming agents, such as the commonly used sodium dodecylsulfate, ...

Alcazar Jorba, Daniel

2012-01-01T23:59:59.000Z

364

Degradation of Ionic Pathway in PEM Fuel Cell Cathode  

SciTech Connect (OSTI)

The degradation of the ionic pathway throughout the catalyst layer in proton exchange membrane fuel cells was studied under an accelerated stress test of catalyst support (potential hold at 1.2 V). Electrochemical behaviors of the cathode based on graphitic mesoporous carbon supported Pt catalyst were examined using electrochemical impedance spectroscopy and cyclic voltammetry. Impedance data were plotted and expressed in the complex capacitance form to determine useful parameters in the transmission line model: the double-layer capacitance, peak frequency, and ionic resistance. Electrochemical surface area and hydrogen crossover current through the membrane were estimated from cyclic voltammogram, while cathode Faradaic resistance was compared with ionic resistance as a function of test time. It was observed that during an accelerated stress test of catalyst support, graphitic mesoporous carbon becomes hydrophilic which increases interfacial area between the ionomer and the catalyst up to 100 h. However, the ionic resistance in the catalyst layer drastically increases after 100 h with further carbon support oxidation. The underlying mechanism has been studied and it was found that significant degradation of ionic pathway throughout the catalyst layer due to catalyst support corrosion induces uneven hydration and mechanical stress in the ionomer.

Park, Seh Kyu; Shao, Yuyan; Wan, Haiying; Viswanathan, Vilayanur V.; Towne, Silas A.; Rieke, Peter C.; Liu, Jun; Wang, Yong

2011-11-12T23:59:59.000Z

365

Characterizing unsaturated diffusion in porous tuff gravel  

SciTech Connect (OSTI)

Evaluation of solute diffusion in unsaturated porous gravel is very important for investigations of contaminant transport and remediation, risk assessment, and waste disposal (for example, the potential high-level nuclear waste repository at Yucca Mountain, Nevada). For a porous aggregate medium such as granular tuff, the total water content is comprised of surface water and interior water. The surface water component (water film around grains and pendular water between the grain contacts) could serve as a predominant diffusion pathway. To investigate the extent to which surface water films and contact points affect solute diffusion in unsaturated gravel, we examined the configuration of water using x-ray computed tomography in partially saturated gravel, and made quantitative measurements of diffusion at multiple water contents using two different techniques. In the first, diffusion coefficients of potassium chloride in 2-4 mm granular tuff at multiple water contents were calculated from electrical conductivity measurements using the Nernst-Einstein equation. In the second, we used laser ablation with inductively coupled plasma-mass spectrometry to perform micro-scale mapping, allowing the measurement of diffusion coefficients for a mixture of chemical tracers for tuff cubes and tetrahedrons having two contact geometries (cube-cube and cube-tetrahedron). The x-ray computed tomography images show limited contact between grains, and this could hinder the pathways for diffusive transport. Experimental results show the critical role of surface water in controlling transport pathways and hence the magnitude of diffusion. Even with a bulk volumetric water content of 1.5%, the measured solute diffusion coefficient is as low as 1.5 x 10{sup -14} m{sup 2}/s for tuff gravel. Currently used diffusion models relating diffusion coefficients to total volumetric water content inadequately describe unsaturated diffusion behavior in porous gravel at very low water contents.

Hu, Qinhong; Kneafsey, Timothy J.; Roberts, Jeffery J.; Tomutsa, Liviu; Wang, Joseph, S.Y.

2003-11-12T23:59:59.000Z

366

Protein separations using porous silicon membranes  

E-Print Network [OSTI]

charge or as the absence of an electron in the crystal structure of silicon. The properties of boron doped siTicon are exploited experimentally by setting up an etch cell in which one surface of the silicon serves as the anode and by using... terminals located on the top surface of the etch cell. The current to be used in the experiment and the total time were previously calculated to produce the desired average pore size and porous silicon film thickness, respectively. The power source...

Pass, Shannon Marie

1992-01-01T23:59:59.000Z

367

A rigid porous filter and filtration method  

SciTech Connect (OSTI)

The present invention involves a porous rigid filter comprising a plurality of concentric filtration elements having internal flow passages and forming external flow passages there between. The present invention also involves a pressure vessel containing the filter for the removal of particulate from high pressure particulate containing gases, and further involves a method for using the filter to remove such particulate. The present filter has the advantage of requiring fewer filter elements due to the high surface area- to-volume ratio provided by the filter, requires a reduced pressure vessel size, and exhibits enhanced mechanical design properties, improved cleaning properties, configuration options, modularity and ease of fabrication.

Chiang, Ta-Kuan; Straub, Douglas, Straub L.; Dennis, Richard A.

1998-12-01T23:59:59.000Z

368

TERMINATION OF THE POROUS WALL CONCEPT To: APEX GROUP  

E-Print Network [OSTI]

TERMINATION OF THE POROUS WALL CONCEPT To: APEX GROUP From: Anter El-Azab (anter@seas.ucla.edu) Re with Lithium will can not work and this concept should be terminated. For the case of vanadium alloy on this concept should be terminated. #12;TERMINATION OF THE POROUS WALL CONCEPT Best Regards, Anter #12;

California at Los Angeles, University of

369

Nitrogen modification of highly porous carbon for improved supercapacitor performance  

E-Print Network [OSTI]

Nitrogen modification of highly porous carbon for improved supercapacitor performance Stephanie L for supercapacitor applications. Surface modification increases the amount of nitrogen by four times when compared elements in highly porous carbon used for electric double-layer supercapacitors.1 These elements modify

Cao, Guozhong

370

Development of an oxidized porous silicon vacuum microtriode  

E-Print Network [OSTI]

the requirements for a gigatron cathode. In the present work, a porous sihcon-based approach is evaluated. The use of porous silicon reduces the size of a single emitter to the manometer scale, and a true two-dimensional array geometry can be approached. A wide...

Smith, Don Deewayne

1994-01-01T23:59:59.000Z

371

Diffusion with dissolution and precipitation in a porous media  

E-Print Network [OSTI]

Diffusion with dissolution and precipitation in a porous media approximation by a finite volume. Quelques tests numériques sont ensuite montrés. KEYWORDS: diffusion, dissolution­precipitation, porous­ ficiency of such disposals relies on material barriers. For such a use, cement concrete offers

Herbin, Raphaèle

372

Diffusion with dissolution and precipitation in a porous media  

E-Print Network [OSTI]

Diffusion with dissolution and precipitation in a porous media approximation by a finite volume numériques sont ensuite montrés. KEYWORDS: diffusion, dissolution-precipitation, porous media, finite volumes barriers. For such a use, cement concrete offers the advantage of having a weak porosity. However, disposal

Herbin, Raphaèle

373

MATHEMATICAL MODELING AND SIMULATION FOR FLUID FLOW IN POROUS MEDIA  

E-Print Network [OSTI]

1 MATHEMATICAL MODELING AND SIMULATION FOR FLUID FLOW IN POROUS MEDIA Ewing, Richard Texas A is to understand the complex chemical, physical, and fluid flow processes occurring in an underground porous medium with one pass through these four steps. Once a computer code has been developed which gives concrete

Ewing, Richard E.

374

Invariant measures for a stochastic porous medium equation  

E-Print Network [OSTI]

Invariant measures for a stochastic porous medium equation Giuseppe Da Prato (Scuola Normale AMS :76S05,35J25, 37L40 . 1 Introduction The porous medium equation X t = (Xm ), m N, (1 Brownian motion in H and C is a positive definite bounded operator on H of trace class. To be more concrete

Röckner, Michael

375

Fundamental studies of fluid mechanics and stability in porous media  

SciTech Connect (OSTI)

This report summarizes accomplished and proposed work for the fundamental studies of fluid mechanics and stability in porous media. Topics discussed include: viscous fingering in miscible displacements; polymer flow interactions in free shear layers of viscoelastic fluids; effect of nonmonotonic viscosity profiles on the stability of miscible displacements in porous media; and references. (JL)

Homsy, G.M.

1991-08-01T23:59:59.000Z

376

Stability of Miscible Displacements Across Stratified Porous Media  

SciTech Connect (OSTI)

This report studied macro-scale heterogeneity effects. Reflecting on their importance, current simulation practices of flow and displacement in porous media were invariably based on heterogeneous permeability fields. Here, it was focused on a specific aspect of such problems, namely the stability of miscible displacements in stratified porous media, where the displacement is perpendicular to the direction of stratification.

Shariati, Maryam; Yortsos, Yanis C.

2000-09-11T23:59:59.000Z

377

Combustion fronts in porous media with two layers Steve Schecter  

E-Print Network [OSTI]

Combustion fronts in porous media with two layers layer 1 layer 2 Steve Schecter North Carolina Subject: Propagation of a combustion front through a porous medium with two parallel layers having different properties. · Each layer admits a traveling combustion wave. · The layers are coupled by heat

Schecter, Stephen

378

Numerical Computation of Multiphase Flows in Porous Media  

E-Print Network [OSTI]

Preface iii Notation ix Introduction 1 1 Modeling Immiscible Fluid Flow in Porous Media 7 1.1 Porous Media legendi im Fachgebiet Informatik (Wissenschaftliches Rechnen) #12;ii #12;Preface Groundwater is a precious resource that is important for all forms of life on earth. The quality of groundwater is impaired

Bastian, Peter

379

Heat exchangers comprising at least one porous member positioned within a casing  

DOE Patents [OSTI]

A heat exchanger and associated methods for sublimating solid particles therein, for conveying fluids therethrough, or both. The heat exchanger includes a chamber, and a porous member having a porous wall having pores in communication with the chamber and an interior of the porous member. A first fluid is conveyed into the porous member while a second fluid is conveyed into the porous member through the porous wall. The second fluid may form a positive flow boundary layer along the porous wall to reduce or eliminate substantial contact between the first fluid and the interior of the porous wall. The combined first and second fluids are conveyed out of the porous member. Additionally, the first fluid and the second fluid may each be conveyed into the porous member at different temperatures and may exit the porous member at substantially the same temperature.

Turner, Terry D. (Idaho Falls, ID); Wilding, Bruce M (Idaho Falls, ID)

2011-11-22T23:59:59.000Z

380

Microwave impregnation of porous materials with thermal energy storage materials  

DOE Patents [OSTI]

A method for impregnating a porous, non-metallic construction material with a solid phase-change material is described. The phase-change material in finely divided form is spread onto the surface of the porous material, after which the porous material is exposed to microwave energy for a time sufficient to melt the phase-change material. The melted material is spontaneously absorbed into the pores of the porous material. A sealing chemical may also be included with the phase-change material (or applied subsequent to the phase-change material) to seal the surface of the porous material. Fire retardant chemicals may also be included with the phase-change materials. The treated construction materials are better able to absorb thermal energy and exhibit increased heat storage capacity.

Benson, David K. (Golden, CO); Burrows, Richard W. (Conifer, CO)

1993-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

Microwave impregnation of porous materials with thermal energy storage materials  

DOE Patents [OSTI]

A method for impregnating a porous, non-metallic construction material with a solid phase-change material is described. The phase-change material in finely divided form is spread onto the surface of the porous material, after which the porous material is exposed to microwave energy for a time sufficient to melt the phase-change material. The melted material is spontaneously absorbed into the pores of the porous material. A sealing chemical may also be included with the phase-change material (or applied subsequent to the phase-change material) to seal the surface of the porous material. Fire retardant chemicals may also be included with the phase-change materials. The treated construction materials are better able to absorb thermal energy and exhibit increased heat storage capacity.

Benson, D.K.; Burrows, R.W.

1993-04-13T23:59:59.000Z

382

Porous Elasticity: Lectures on the elasticity of porous materials as an application of the theory of mixtures  

E-Print Network [OSTI]

of classical porous media models. Chapter 2 introduces the essentials of the theory of mixtures. Chapters 3,4 and 5 exploit the theory of mixtures to formulate various models of porous elastic materials. Chapter 6 is concerned with establishing connections...

Bowen, Ray M.

2014-01-22T23:59:59.000Z

383

Multicomponent Gas Diffusion in Porous Electrodes  

E-Print Network [OSTI]

Multicomponent gas transport is investigated with unprecedented precision by AC impedance analysis of porous YSZ anode-supported solid oxide fuel cells. A fuel gas mixture of H2-H2O-N2 is fed to the anode, and impedance data are measured across the range of hydrogen partial pressure (10-100%) for open circuit conditions at three temperatures (800C, 850C and 900C) and for 300mA applied current at 800C. For the first time, analytical formulae for the diffusion resistance (Rb) of three standard models of multicomponent gas transport (Fick, Stefan-Maxwell, and Dusty Gas) are derived and tested against the impedance data. The tortuosity is the only fitting parameter since all the diffusion coefficients are known. Only the Dusty Gas model leads to a remarkable data collapse for over twenty experimental conditions, using a constant tortuosity consistent with permeability measurements and the Bruggeman relation. These results establish the accuracy of the Dusty Gas model for multicomponent gas diffusion in porous med...

Fu, Yeqing; Dutta, Abhijit; Mohanram, Aravind; Pietras, John D; Bazant, Martin Z

2014-01-01T23:59:59.000Z

384

Conductive Filler Morphology Effect on Performance of Ionic Polymer Conductive Network Composite Actuators  

E-Print Network [OSTI]

Several generations of ionic polymer metal composite (IPMC) actuators have been developed since 1992. It has been discovered that the composite electrodes which are composed of electronic and ionic conductors, have great ...

Liu, Sheng

385

Characterization of ionic liquid ion sources for focused ion beam applications  

E-Print Network [OSTI]

In the Focused Ion Beam (FIB) technique, a beam of ions is reduced to nanometer dimensions using dedicated optics and directed to a substrate for patterning. This technique is widely used in micro- and nanofabrication for ...

Perez Martinez, Carla S. (Carla Sofia)

2013-01-01T23:59:59.000Z

386

Force microscopy of layering and friction in an ionic liquid Judith Hotha,b  

E-Print Network [OSTI]

shape of the force vs. distance curve is explained by a model for the interaction between tip, gold of the compliant force sensor between branches of the oscillatory force curve. Frictional force between-viscosity, yet load- bearing lubricant [1-4]. The load-bearing ability stems from the formation of solvation

Mueser, Martin

387

Studies of Block Copolymer Thin Films and Mixtures with an Ionic Liquid  

E-Print Network [OSTI]

identification of structure and domain size in block copolymer thin films using RSoXS enables a quantitative comparison of the bulk

Virgili, Justin

2009-01-01T23:59:59.000Z

388

High-Performance Supercapacitors Based on Poly(ionic liquid)-Modified  

E-Print Network [OSTI]

- pected for an ideal graphene-based super- capacitor.6 Moreover, current supercapaci- tors have energy for super- capacitors assembled with graphene-based electrodes. One of the challenges is achiev- ing-layer capacitors or ultracapac- itors) are electrochemical capacitors that store energy through reversible ion ad

389

Synthesis of three advanced biofuels from ionic liquid-pretreated switchgrass using engineered Escherichia coli  

E-Print Network [OSTI]

One approach to reducing the costs of advanced biofuel production from cellulosic biomass is to engineer a single microorganism to both digest plant biomass and produce hydrocarbons that have the properties of petrochemical ...

Bokinsky, Gregory

390

Environmentally Benign Production of Ionic Liquids in CO2-Expanded Systems  

E-Print Network [OSTI]

of [HMIm][Br]). Although DMSO is a relatively environmentally benign solvent, it is beset with a high boiling point (189oC), rendering it both economically and environmentally non-feasible as a solvent option. The synthesis and processing of ILs in gas...

Nwosu, Sylvia Ogechi

2012-08-31T23:59:59.000Z

391

Recovery of Sugars from Ionic Liquid Biomass Liquor by Solvent Extraction  

E-Print Network [OSTI]

Bioenerg. Res. (2010) 3:123–133 DOI 10.1007/s12155-010-9091-has been shown to be an Bioenerg. Res. (2010) 3:123–133 12.Division, Joint BioEnergy Institute, Emeryville, CA, USA e-

Brennan, Timothy C.; Datta, Supratim; Blanch, Harvey W.; Simmons, Blake A.; Holmes, Bradley M.

2010-01-01T23:59:59.000Z

392

Investigations into the Synthesis, Identification and Developability of Active Ionic Liquids  

E-Print Network [OSTI]

to be advantageous in traditional oral and alternative non-oral routes of administration. The library of successful AILs was increased with a series of generic and propriatary compounds. They were characterized via infrared spectrometry, glass transition temperature...

Miller, Elise

2012-12-31T23:59:59.000Z

393

Homogeneous Hydrogenation of CO2 to Methyl Formate Utilizing Switchable Ionic Liquids  

SciTech Connect (OSTI)

Capture of CO2 and subsequent hydrogenation allows for base/alcohol-catalyzed conversion of CO2 to methylformate in one pot. The conversion of CO2 proceeds via alkylcarbonates, to formate salts and then formate esters, which can be catalyzed by base and alcohol with the only byproduct being water. The system operates at mild conditions (300 psi H2, 140 ?C). Reactivity is strongly influenced by temperature and choice of solvent. In the presence of excess of base (DBU) formate is predominant product while in excess of methanol methyl formate is major product. 110 ?C yields formate salts, 140 ?C promotes methylformate. The authors acknowledge internal Laboratory Directed Re-search and Development (LDRD) funding from Pacific Northwest National Laboratory (PNNL). PNNL is operated by Battelle for the U.S. Department of Energy.

Yadav, Mahendra (ORCID:0000000202660382); Linehan, John C.; Karkamkar, Abhijeet J.; Van Der Eide, Edwin F.; Heldebrant, David J.

2014-09-15T23:59:59.000Z

394

Identification of a haloalkaliphilic and thermostable cellulase with improved ionic liquid tolerance  

E-Print Network [OSTI]

acetate ([Emim]Ac), 1-ethyl-3-methylimidazolium chloride ([Emim]Cl), 1-butyl-3-methylimidazolium chloride ([Bmim]Cl) and 1-allyl-

Zhang, Tao

2012-01-01T23:59:59.000Z

395

Studies of ionic liquids in lithium-ion battery test systems  

E-Print Network [OSTI]

are not useful for lithium batteries. We are therefore nowapplications using lithium batteries, we must be sure thattemperature range. For lithium batteries in hybrid vehicles,

Salminen, Justin; Prausnitz, John M.; Newman, John

2006-01-01T23:59:59.000Z

396

Gas Hydrate Equilibrium Measurements for Multi-Component Gas Mixtures and Effect of Ionic Liquid Inhibitors  

E-Print Network [OSTI]

hydrate inhibition data from a newly commissioned micro bench top reactor, a high-pressure autoclave and a rocking cell. The conditions for hydrate formation for pure methane and carbon dioxide were also measured, for validation purposes. The measured data...

Othman, Enas Azhar

2014-04-07T23:59:59.000Z

397

Technical Highlights for July 2012 New Collaboration Underway to Investigate Ionic Liquids for Enhancing Engine Efficiency  

E-Print Network [OSTI]

for Enhancing Engine Efficiency A new Cooperative Research and Development Agreement (CRADA), No. NFE-12

398

Ionic Liquids as Multi-Functional Lubricant Additives to Enhance Engine Efficiency  

Broader source: Energy.gov [DOE]

2013 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting

399

Studies of Block Copolymer Thin Films and Mixtures with an Ionic Liquid  

E-Print Network [OSTI]

based natural materials, 4 dye-sensitized solar cells, 5 andcells, 4-8 and dye-sensitized solar cells. 9-12 While the

Virgili, Justin

2009-01-01T23:59:59.000Z

400

Ionic liquid assisted electrospinning of quantum dots/elastomer composite Jiahua Zhu a  

E-Print Network [OSTI]

,* a Integrated Composites Laboratory (ICL), Dan F. Smith Department of Chemical Engineering, Lamar University, Beaumont, TX 77710, USA b Department of Chemistry and Biochemistry, Lamar University, Beaumont, TX 77710, USA c Department of Biology, Lamar University, Beaumont, TX 77710, USA d Ocean NanoTech, LLC, 2143

Guo, John Zhanhu

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

Separable fluorous ionic liquids for the dissolution and saccharification of cellulose  

E-Print Network [OSTI]

Cellulose (medium cotton linters, C6288) was from Sigma Chemical (St. Louis, MO). Other commercial chemicals silica gel was from Aldrich Chemical (Milwaukee, WI). The term "concentrated under reduced pressure unless indicated otherwise. Mass spectrometry was performed with a Micromass LCT (electrospray ionization

Raines, Ronald T.

402

Ionic Liquids as an Attractive Alternative Solvent for Thermal Lens Measurements  

E-Print Network [OSTI]

in volatile organic solvents such as benzene, carbon tetrachloride, and hexane. However, the ILs are more,2 Nonpolar, volative organic solvents such as benzene, carbon tetrachloride, and hexane should provide good

Reid, Scott A.

403

Ionic Liquids Used as Wear Reduction, Wins R&D 100 Award | Department of  

Broader source: Energy.gov (indexed) [DOE]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) "of EnergyEnergyENERGYWomentheATLANTA,Fermi NationalBusinessDepartmentat Larger Scale | Department

404

Surface layering and melting in an ionic liquid studied by resonant soft  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary)morphinanInformation Desert Southwest RegionatSearchScheduled System Burst Buffer ArchiveSuppliers Suppliers

405

Toward a Materials Genome Approach for Ionic Liquids: Synthesis Guided by  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary)morphinanInformation Desert Southwest RegionatSearchScheduled System BurstLongTitan Titan is aSurface Area

406

Development of a Universal Method Based on Ionic Liquids for Determination of  

E-Print Network [OSTI]

at room temperature. They have unique chemical and physical properties, including being air and moisture of Enantiomeric Compositions of Pharmaceutical Products Chieu D. Tran* Department of Chemistry, Marquette with either new anions and/or cations and determining © 2010 American Chemical Society Downloadedby

Reid, Scott A.

407

Computer simulations of ionic liquids at electrochemical interfaces C. Merlet1,2  

E-Print Network [OSTI]

emphasizing the case of elec- trical double layer capacitors (EDLC), which has at- tracted much attention

Paris-Sud XI, Université de

408

Imaging an ionic liquid adlayer by scanning tunneling microscopy at the solid|vacuum interface  

E-Print Network [OSTI]

of Surface Chemistry and Catalysis, Ulm University, D-89069 Ulm, Germany 2 Institute of Particle Technology, Clausthal University of Technology, D-38678 Clausthal- Zellerfeld, Gemany Abstract The first imaging(pentafluoroethyl)trifluorophosphate ([Py1,4]FAP) was evaporated onto a clean Au(111) surface by a Knudsen-type evaporator and the surface

Pfeifer, Holger

409

New lithium-based ionic liquid electrolytes that resist salt concentration  

Energy Savers [EERE]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Office of Inspector General Office0-72.pdfGeorgeDoesn't32DepartmentWells |of Energypolarization | Department of

410

Ionic Liquid-Enhanced Solid State Electrolyte Interface (SEI) for Lithium  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFunInfrared LandResponsesIon/Surface Reactions and Ion Soft-Landing.OxfordSulfur

411

Ionic Liquids as New Solvents for Improved Separation of Medical Isotopes -  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFunInfrared LandResponsesIon/Surface Reactions and IonEnergy Innovation

412

Understanding the effect of side groups in ionic liquids on carbon-capture  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary)morphinanInformation Desert Southwest RegionatSearchScheduledProduction Undergraduateproperties: a combined

413

Inexpensive, Nonfluorinated (or Partially Fluorinated) Anions for Lithium Salts and Ionic Liquids for Lithium Battery Electrolytes  

Broader source: Energy.gov [DOE]

2013 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer Evaluation Meeting

414

Safetygram #9- Liquid Hydrogen  

Broader source: Energy.gov [DOE]

Hydrogen is colorless as a liquid. Its vapors are colorless, odorless, tasteless, and highly flammable.

415

Quantification of Liquid Water Saturation in a PEM Fuel Cell Diffusion Medium Using X-ray Microtomography  

E-Print Network [OSTI]

Quantification of Liquid Water Saturation in a PEM Fuel Cell Diffusion Medium Using X understanding of the two-phase flow and flooding occurrence in proton exchange membrane PEM fuel cells. We have as ice formation during cold start of PEM fuel cells. The water present in these porous layers

416

E-Print Network 3.0 - alginate microparticle ionic Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Naturally Summary: , crosslinked'' indicates alginate was crosslinked with CaCl2, and uncrosslinked'' indicates ionic crosslinks... ), and alginate, a...

417

A Semi-Empirical Model for Porous Media Heat Exchanger Design Richard A. Wirtz1  

E-Print Network [OSTI]

and the effectiveness of the porous wall are always maximum when it is operated with the number of transfer units of the porous matrix greater than two (ntu 2). Furthermore, if the porous matrix is composed of a packed bed matrix is minimum when ntu 2. This suggest that for many design requirements, the porous media exchanger

Wirtz, Richard A.

418

Macrodispersivity tensor for nonreactive solute transport in isotropic and anisotropic fractal porous media  

E-Print Network [OSTI]

porous media: Analytical solutions Hongbin Zhan1 and Stephen W. Wheatcraft Hydrology/Hydrogeology Program

Zhan, Hongbin

419

Towards improved methods for determining porous media multiphase flow functions  

E-Print Network [OSTI]

to the empirical relation by using the three-dimensional saturation and relaxation data. 7 CHAPTER II ESTIMATION OF POROUS MEDIA FLOW FUNCTIONS Multiphase flow functions are required to simulate the flow of multiple fluid phases through porous media....3) Snw + Sw = 1: (2.4) Together with boundary and initial conditions, Eqs. (2.1)-(2.4) provide a mathemat- ical model of three-dimensional, two-phase fluid flow in porous media. Several properties have to be specified in the above model. The densities...

Xue, Song

2004-09-30T23:59:59.000Z

420

Rapid process for producing transparent, monolithic porous glass  

DOE Patents [OSTI]

A process for making transparent porous glass monoliths from gels. The glass is produced much faster and in much larger sizes than present technology for making porous glass. The process reduces the cost of making large porous glass monoliths because: 1) the process does not require solvent exchange nor additives to the gel to increase the drying rates, 2) only moderate temperatures and pressures are used so relatively inexpensive equipment is needed, an 3) net-shape glass monoliths are possible using this process. The process depends on the use of temperature to control the partial pressure of the gel solvent in a closed vessel, resulting in controlled shrinking during drying.

Coronado, Paul R. (Livermore, CA)

2006-02-14T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


421

Theory of Sound Propagation in Superfluid Solutions Filled Porous Media  

E-Print Network [OSTI]

A theory of the propagation of acoustic waves in a porous medium filled with superfluid solution is developed. The elastic coefficients in the system of equations are expressed in terms of physically measurable quantities. The equations obtained describe all volume modes that can propagate in a porous medium saturated with superfluid solution. Finally, derived equations are applied to the most important particular case when the normal fluid component is locked inside a highly porous media (aerogel) by viscous forces and the velocities of two longitudinal sound modes are calculated.

Sh. E. Kekutia; N. D. Chkhaidze

2005-02-10T23:59:59.000Z

422

The porous atmosphere of eta Carinae  

E-Print Network [OSTI]

We analyze the wind generated by the great 20 year long super-Eddington outburst of eta-Carinae. We show that using classical stellar atmospheres and winds theory, it is impossible to construct a consistent wind model in which a sufficiently small amount of mass, like the one observed, is shed. One expects the super-Eddington luminosity to drive a thick wind with a mass loss rate substantially higher than the observed one. The easiest way to resolve the inconsistency is if we alleviate the implicit notion that atmospheres are homogeneous. An inhomogeneous atmosphere, or "porous", allows more radiation to escape while exerting a smaller average force. Consequently, such an atmosphere yields a considerably lower mass loss rate for the same total luminosity. Moreover, all the applications of the Eddington Luminosity as a strict luminosity limit should be revised, or at least reanalyzed carefully.

Nir J. Shaviv

2000-02-09T23:59:59.000Z

423

Flow in porous media, phase and ultralow interfacial tensions: Mechanisms of enhanced petroleum recovery  

SciTech Connect (OSTI)

A major program of university research, longer-ranged and more fundamental in approach than industrial research, into basic mechanisms of enhancing petroleum recovery and into underlying physics, chemistry, geology, applied mathematics, computation, and engineering science has been built at Minnesota. The original focus was surfactant-based chemical flooding, but the approach taken was sufficiently fundamental that the research, longer-ranged than industrial efforts, has become quite multidirectional. Topics discussed are volume controlled porosimetry; fluid distribution and transport in porous media at low wetting phase saturation; molecular dynamics of fluids in ultranarrow pores; molecular dynamics and molecular theory of wetting and adsorption; new numerical methods to handle initial and boundary conditions in immiscible displacement; electron microscopy of surfactant fluid microstructure; low cost system for animating liquid crystallites viewed with polarized light; surfaces of constant mean curvature with prescribed contact angle.

Davis, H.T.; Scriven, L.E.

1991-07-01T23:59:59.000Z

424

Liquid level detector  

DOE Patents [OSTI]

A liquid level detector for low pressure boilers. A boiler tank, from which apor, such as steam, normally exits via a main vent, is provided with a vertical side tube connected to the tank at the desired low liquid level. When the liquid level falls to the level of the side tube vapor escapes therethrough causing heating of a temperature sensitive device located in the side tube, which, for example, may activate a liquid supply means for adding liquid to the boiler tank. High liquid level in the boiler tank blocks entry of vapor into the side tube, allowing the temperature sensitive device to cool, for example, to ambient temperature.

Grasso, Albert P. (Vernon, CT)

1986-01-01T23:59:59.000Z

425

Liquid level detector  

DOE Patents [OSTI]

A liquid level detector for low pressure boilers. A boiler tank, from which vapor, such as steam, normally exits via a main vent, is provided with a vertical side tube connected to the tank at the desired low liquid level. When the liquid level falls to the level of the side tube vapor escapes therethrough causing heating of a temperature sensitive device located in the side tube, which, for example, may activate a liquid supply means for adding liquid to the boiler tank. High liquid level in the boiler tank blocks entry of vapor into the side tube, allowing the temperature sensitive device to cool, for example, to ambient temperature.

Grasso, A.P.

1984-02-21T23:59:59.000Z

426

Uncertainty quantification using multiscale methods for porous media flows  

E-Print Network [OSTI]

numerical models. When solving the flow and transport through heterogeneous porous media some type of upscaling or coarsening is needed due to scale disparity. We describe multiscale techniques used for solving the spatial component of the stochastic flow...

Dostert, Paul Francis

2009-05-15T23:59:59.000Z

427

Colloid-facilitated radionuclide transport in fractured porous rock  

E-Print Network [OSTI]

Numerical methods have been applied for the prediction of colloid-facilitated radionuclide transport through water-saturated fractured porous rock. The presence of colloids may enhance the transport of radionuclides in groundwater by reducing...

Baek, Inseok

1994-01-01T23:59:59.000Z

428

Effective hydraulic conductivity of bounded, strongly heterogeneous porous media  

E-Print Network [OSTI]

Effective hydraulic conductivity of bounded, strongly heterogeneous porous media Evangelos K of Arizona, Tucson Abstract. We develop analytical expressions for the effective hydraulic conductivity Ke boundaries. The log hydraulic conductivity Y forms a Gaussian, statistically homogeneous and anisotropic

Tartakovsky, Daniel M.

429

Ultrasonic measurement of porous medium in an aqueous environment  

E-Print Network [OSTI]

The use of a medical ultrasonic scanning device was studied as a measuring tool for determining the physical characteristics of soft porous media in an turbid aqueous environment. Three different sponge types were used as the soft objects. A method...

Daubon, Jose C

1995-01-01T23:59:59.000Z

430

Gasification and combustion modeling for porous char particles  

E-Print Network [OSTI]

Gasification and combustion of porous char particles occurs in many industrial applications. Reactor-scale outputs of importance depend critically on processes that occur at the particle-scale. Because char particles often ...

Singer, Simcha Lev

2012-01-01T23:59:59.000Z

431

Functionalization/passivation of porous graphitic carbon with...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

data are also presented. Citation: Jensen DS, V Gupta, RE Olsen, AT Miller, RC Davis, D Ess, Z Zhu, MA Vail, A Dadson, and MR Linford.2011."Functionalizationpassivation of porous...

432

Carbide-derived carbons - From porous networks to nanotubes and...  

Office of Scientific and Technical Information (OSTI)

Carbide-derived carbons - From porous networks to nanotubes and graphene Re-direct Destination: Carbide-derived carbons (CDCs) are a large family of carbon materials derived from...

433

Field emission study of cobalt ion implanted porous silicon  

E-Print Network [OSTI]

Porous silicon has become potentially important material for microelectronics applications. By using low energy implantation and energy scan implantation, a stable silicide with good electrical conductivity can be formed, and can be used...

Liu, Hongbiao

1995-01-01T23:59:59.000Z

434

Simulation of filtration for suspension transport in porous media  

E-Print Network [OSTI]

This thesis describes the development and application of a novel method for analyzing the filtration of particles transported through a granular porous medium. The proposed analysis considers the deposition of particles ...

Kim, Yun Sung, 1974-

2005-01-01T23:59:59.000Z

435

The evolution of miscible gravity currents in horizontal porous layers  

E-Print Network [OSTI]

Gravity currents of miscible fluids in porous media are important to understand because they occur in important engineering projects, such as enhanced oil recovery and geologic CO[subscript 2] sequestration. These flows ...

Szulczewski, Michael Lawrence

436

Vortex development behind a finite porous obstruction in a channel  

E-Print Network [OSTI]

This experimental study describes the turbulent wake behind a two-dimensional porous obstruction, consisting of a circular array of cylinders. The cylinders extend from the channel bed through the water surface, mimicking ...

Zong, Lijun

437

Experimental design for study of nucleate boiling in porous structures  

E-Print Network [OSTI]

The superheat required to initiate nucleate boiling inside porous wicks is not well understood in practice. This thesis reports the design of an experimental setup for investigating the onset of vapor nucleation in sintered ...

Kelley, Mitchell Joseph

2011-01-01T23:59:59.000Z

438

Liquid Hydrogen Absorber for MICE  

E-Print Network [OSTI]

REFERENCES Figure 5: Liquid hydrogen absorber and test6: Cooling time of liquid hydrogen absorber. Eight CernoxLIQUID HYDROGEN ABSORBER FOR MICE S. Ishimoto, S. Suzuki, M.

Ishimoto, S.

2010-01-01T23:59:59.000Z

439

Porous solid ion exchange wafer for immobilizing biomolecules  

DOE Patents [OSTI]

A porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer. Also disclosed is a porous solid ion exchange wafer having a combination of a biomolecule capture-resin and an ion-exchange resin forming a charged capture resin within said wafer containing a biomolecule with a tag. A separate bioreactor is also disclosed incorporating the wafer described above.

Arora, Michelle B. (Woodridge, IL); Hestekin, Jamie A. (Morton Grove, IL); Lin, YuPo J. (Naperville, IL); St. Martin, Edward J. (Libertyville, IL); Snyder, Seth W. (Lincolnwood, IL)

2007-12-11T23:59:59.000Z

440

Nuclear magnetic resonance study of methane adsorbed on porous silicon  

E-Print Network [OSTI]

NUCLEAR MAGNETIC RESONANCE STUDY OF METHANE ADSORBED ON POROUS SILICON A Thesis by FENG I I Submitted to the Office of Graduate Studies of Texas ARM University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE... May 1992 Major Subject: Physics NUCLEAR MAGNETIC RESONANCE STUDY OF METHANE ADSORBED ON POROUS SILICON A Thesis by FENG LI Approved as to style and content by: . P. Kirk (Chair of Committee) i G. Agnolet (Member) J. H. Ross, r (Member) M...

Li, Feng

1992-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


441

The study of methane adsorbed on porous silicon by NMR  

E-Print Network [OSTI]

THE STUDY OF METHANE ADSORBED ON POROUS SILICON BY NMR A Thesis by ADAM KAZIMIERZ CZERMAK Submitted to the Graduate College of Texas ARM University in partial fulfillment of the requirement for the degree of MASTER OF SCIENCE August 1986... Major Subject: Physics THE STUDY OF METHANE ADSORBED ON POROUS SILICON BY NMR A Thesis by ADAM KAZIMIERZ CZERMAK Approved as to style and content by: e Wile . Kirk (Chairman of Committee) J eevak M. Par pi a (Member) Randall L. Geiger...

Czermak, Adam Kazimierz

1986-01-01T23:59:59.000Z

442

Two dimensional properties of methane adsorbed on porous silicon  

E-Print Network [OSTI]

TWO DIMENSIONAL PROPERTIES OF METHANE ADSORBED ON POROUS SILICON A Thesis by RICHARD FRANKLIN TENNIS Submitted to the Office of Graduate Studies of Texas ASM University in partial fulfillment of the requirements for the degree of MASTER... OF SCIENCE May 1989 Major Subject: Physics TWO DIMENSIONAL PROPERTIES OF METHANE ADSORBED ON POROUS SILICON A Thesis by RICHARD FRANKLIN TENNIS Approved as to style and content by: P. Kirk (C ir of Committee) Glenn olet (M er) Da J. Ernst...

Tennis, Richard Franklin

1989-01-01T23:59:59.000Z

443

Guidance Document Cryogenic Liquids  

E-Print Network [OSTI]

with air. Liquid carbon monoxide is extremely toxic and extremely flammable. #12;Cryogenic liquids connecting cylinder to lower pressure piping or systems. 6. Use a check valve or trap in the discharge line

444

Monodisperse porous polymer particles containing macrocyclic ether as a new class of sorbent for SR(II) separation  

SciTech Connect (OSTI)

Strontium{sup 90} is one of the typical fission products that may be found in high level liquid waste (HLLW). Separation of Sr{sup 90} prior to the vitrification is beneficial to the final treatment of solid radioactive waste. In this study, a new class of sorbent for Sr(II) was developed by loading the macrocyclic ether DtBuCH18C6 into the monodisperse porous polymer particles (MPPPs). The MPPPs are well-known as a promising chromatographic material due to the uniform particle size, porous morphology, good compatibility with organic extractants, and rigid matrix. The structure and micro-morphology of the sorbent particles were characterized. The adsorption behavior towards Sr(II) in HNO{sub 3} media was investigated by both batch and column experiments. High adsorption efficiency and selective separation of Sr(II) was obtained. The sorbent particles can be recycled for at least several times before obvious lose of the adsorption ability. This kind of sorbent possesses the potential to be used for strontium separation in radioactive liquid waste.

Leng, Yuxiao; Bai, Feifei [Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing 100084 (China); Faculty of Chemical Science and Engineering, China University of Petroleum, Beijing 100084 (China); Ye, Gang; Wei, Jichao; Wang, Jianchen; Chen, Jing [Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing 100084 (China)

2013-07-01T23:59:59.000Z

445

Equation for liquid density  

SciTech Connect (OSTI)

Saturated liquid densities for organic chemicals are given as functions of temperature using a modified Rackett equation.

Yaws, C.L.; Yang, H.C.; Hopper, J.R.; Cawley, W.A. (Lamar Univ., Beaumont, TX (US))

1991-01-01T23:59:59.000Z

446

Liquid detection circuit  

DOE Patents [OSTI]

Herein is a circuit which is capable of detecting the presence of liquids, especially cryogenic liquids, and whose sensor will not overheat in a vacuum. The circuit parameters, however, can be adjusted to work with any liquid over a wide range of temperatures.

Regan, Thomas O. (North Aurora, IL)

1987-01-01T23:59:59.000Z

447

Non-Fickian ionic diffusion across high-concentration gradients  

SciTech Connect (OSTI)

A non-Fickian physico-chemical model for electrolyte transport in high-ionic strength systems is developed and tested with laboratory experiments with copper sulfate as an example electrolyte. The new model is based on irreversible thermodynamics and uses measured mutual diffusion coefficients, varying with concentration. Compared to a traditional Fickian model, the new model predicts less diffusion and asymmetric diffusion profiles. Laboratory experiments show diffusion rates even smaller than those predicted by our non-Fickian model, suggesting that there are additional, unaccounted for processes retarding diffusion. Ionic diffusion rates maybe a limiting factor in transporting salts whose effect on fluid density will in turn significantly affect the flow regime. These findings have important implications for understanding and predicting solute transport in geologic settings where dense, saline solutions occur. 30 refs., 5 figs.

Carey, A.E.; Wheatcraft, S.W. [Univ. of Nevada, Reno, NV (United States)] [Univ. of Nevada, Reno, NV (United States); Glass, R.J. [Sandia National Laboratory, Albuquerque, NM (United States)] [and others] [Sandia National Laboratory, Albuquerque, NM (United States); and others

1995-09-01T23:59:59.000Z

448

Thermodynamics and Ionic Conductivity of Block Copolymer Electrolytes  

E-Print Network [OSTI]

B. and J. Garche, Lithium batteries: Status, prospects andionic liquids for lithium batteries. Journal of Powersolid-state rechargeable lithium batteries. Journal of the

Wanakule, Nisita Sidra

2010-01-01T23:59:59.000Z

449

Liquid Metal Transformers  

E-Print Network [OSTI]

The room temperature liquid metal is quickly emerging as an important functional material in a variety of areas like chip cooling, 3D printing or printed electronics etc. With diverse capabilities in electrical, thermal and flowing behaviors, such fluid owns many intriguing properties that had never been anticipated before. Here, we show a group of unconventional phenomena occurring on the liquid metal objects. Through applying electrical field on the liquid metals immersed in water, a series of complex transformation behaviors such as self-assembling of a sheet of liquid metal film into a single sphere, quick mergences of separate metal droplets, controlled self-rotation and planar locomotion of liquid metal objects can be realized. Meanwhile, it was also found that two accompanying water vortexes were induced and reliably swirled near the rotating liquid metal sphere. Further, effects of the shape, size, voltage, orientation and geometries of the electrodes to control the liquid metal transformers were clar...

Sheng, Lei; Liu, Jing

2014-01-01T23:59:59.000Z

450

Porous platinum-based catalysts for oxygen reduction  

DOE Patents [OSTI]

A porous metal that comprises platinum and has a specific surface area that is greater than 5 m.sup.2/g and less than 75 m.sup.2/g. A fuel cell includes a first electrode, a second electrode spaced apart from the first electrode, and an electrolyte arranged between the first and the second electrodes. At least one of the first and second electrodes is coated with a porous metal catalyst for oxygen reduction, and the porous metal catalyst comprises platinum and has a specific surface area that is greater than 5 m.sup.2/g and less than 75 m.sup.2/g. A method of producing a porous metal according to an embodiment of the current invention includes producing an alloy consisting essentially of platinum and nickel according to the formula Pt.sub.xNi.sub.1-x, where x is at least 0.01 and less than 0.3; and dealloying the alloy in a substantially pH neutral solution to reduce an amount of nickel in the alloy to produce the porous metal.

Erlebacher, Jonah D; Snyder, Joshua D

2014-11-25T23:59:59.000Z

451

Capture and release of mixed acid gasses with binding organic liquids  

DOE Patents [OSTI]

Reversible acid-gas binding organic liquid systems that permit separation and capture of one or more of several acid gases from a mixed gas stream, transport of the liquid, release of the acid gases from the ionic liquid and reuse of the liquid to bind more acid gas with significant energy savings compared to current aqueous systems. These systems utilize acid gas capture compounds made up of strong bases and weak acids that form salts when reacted with a selected acid gas, and which release these gases when a preselected triggering event occurs. The various new materials that make up this system can also be included in various other applications such as chemical sensors, chemical reactants, scrubbers, and separators that allow for the specific and separate removal of desired materials from a gas stream such as flue gas.

Heldebrant, David J. (Richland, WA); Yonker, Clement R. (Kennewick, WA)

2010-09-21T23:59:59.000Z

452

An experimental measurement of the thermal conductivity and diffusivity of a porous solid-liquid system  

E-Print Network [OSTI]

to contain the sample for the flow rate measurement. 1. Air Supply 2 ~ Vacuun Line 3. Waste Line 4 ~ Surge Tank 5. Water Reservoir 6. Oil Reservoir Test Specinsn 8. Pressure Regulator Valve SATURATION APPARATUS FCR SATURATI?l SARDSTONR TXSP... the system can be described by' the one h dimensional form of Fouriers dT Equation: Q ~ -!:. A ? . ds The quantity of heat flowing through the oil and water in the pore dT space is OCk! ~ K A& ( ? ) + Kp AC (~)C ~ Based on the unidirectional W & d...

Dunn, James Elliott

1959-01-01T23:59:59.000Z

453

Syngas production from heavy liquid fuel reforming in inert porous media  

E-Print Network [OSTI]

-up), but it will still show a significant efficiency advantage [2]. Eventually, when fuel cells and hydrogen demand will build up, a switch can be made to central hydrogen production, by using fossil sources with CO2 sequestration and finally by the use of low carbon... requirements: • Hydrogen production levels smaller than those in chemical plants; • Severe constraints on size and weight; • Ability to cycle through frequent start-ups and shutdowns; • Hydrogen production rate should be responsive to changes in demand...

Pastore, Andrea

2010-11-16T23:59:59.000Z

454

Flow adjustment and interior flow associated with a rectangular porous obstruction  

E-Print Network [OSTI]

The flow at the leading edge and in the interior of a rectangular porous obstruction is described through experiments and scaling. The porous obstruction consists of an emergent, rectangular array of cylinders in shallow ...

Rominger, Jeffrey Tsaros

455

Discrete particle transport in porous media : discrete observations of physical mechanisms influencing particle behavior  

E-Print Network [OSTI]

An understanding of how discrete particles in the micron to submicron range behave in porous media is important to a number of environmental problems. Discrete particle behavior in the interior of a porous medium is complex ...

Yoon, Joon Sik, 1973-

2005-01-01T23:59:59.000Z

456

NERSC Analysis of Void Space of Porous Materials Used in Energy...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Porous Materials Analysis of Void Space of Porous Materials Used in Energy-related Applications fmm-smmaciek.jpg We have developed partial differential equations-based tools that...

457

Phenomenological study of Au and Pt nanowires grown in porous alumina scaffolds  

E-Print Network [OSTI]

Porous anodic aluminum oxide, commonly known as AAO, has been widely used as a scaffold to synthesize nanowires and nanotubes. The porous alumina structure can be obtained from a simple electrochemical oxidation process, ...

Shin, Yong Cheol, S.M. Massachusetts Institute of Technology

2011-01-01T23:59:59.000Z

458

Highly porous chemically modified carbon cryogels and their coherent nanocomposites for energy applications  

E-Print Network [OSTI]

the pores, porous media for natural gas (methane) storage at reduced pressure, and scaffolds for hydride the pores, porous media for natural gas (m of Mechanical Science and Engineering, Huazhong University of Science & Technology, Wuhan, 430074, China d

Cao, Guozhong

459

Thin Porous Metal Sheet-Supported NaA Zeolite Membrane for Water...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Thin Porous Metal Sheet-Supported NaA Zeolite Membrane for WaterEthanol Separation. Thin Porous Metal Sheet-Supported NaA Zeolite Membrane for WaterEthanol Separation. Abstract:...

460

Study of gas flow dynamics in porous and granular media with laser-polarized ¹²?Xe NMR  

E-Print Network [OSTI]

This thesis presents Nuclear Magnetic Resonance (NMR) studies of gas flow dynamics in porous and granular media by using laser-polarized ¹²?Xe . Two different physical processes, the gas transport in porous rock cores and ...

Wang, Ruopeng, 1972-

2005-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


461

Hollow Core-Shell Structured Porous Si-C Nanocomposites for Li...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Hollow Core-Shell Structured Porous Si-C Nanocomposites for Li-Ion Battery Anodes. Hollow Core-Shell Structured Porous Si-C Nanocomposites for Li-Ion Battery Anodes. Abstract:...

462

E-Print Network 3.0 - antimony oxide ionic Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

results for: antimony oxide ionic Page: << < 1 2 3 4 5 > >> 1 IOP PUBLISHING NANOTECHNOLOGY Nanotechnology 20 (2009) 264003 (7pp) doi:10.10880957-44842026264003 Summary:...

463

Porous siliconformation and etching process for use in silicon micromachining  

DOE Patents [OSTI]

A reproducible process for uniformly etching silicon from a series of micromechanical structures used in electrical devices and the like includes providing a micromechanical structure having a silicon layer with defined areas for removal thereon and an electrochemical cell containing an aqueous hydrofluoric acid electrolyte. The micromechanical structure is submerged in the electrochemical cell and the defined areas of the silicon layer thereon are anodically biased by passing a current through the electrochemical cell for a time period sufficient to cause the defined areas of the silicon layer to become porous. The formation of the depth of the porous silicon is regulated by controlling the amount of current passing through the electrochemical cell. The micromechanical structure is then removed from the electrochemical cell and submerged in a hydroxide solution to remove the porous silicon. The process is subsequently repeated for each of the series of micromechanical structures to achieve a reproducibility better than 0.3%.

Guilinger, Terry R. (Albuquerque, NM); Kelly, Michael J. (Albuquerque, NM); Martin, Jr., Samuel B. (Albuquerque, NM); Stevenson, Joel O. (Albuquerque, NM); Tsao, Sylvia S. (Albuquerque, NM)

1991-01-01T23:59:59.000Z

464

An electrochemical route for making porous nickel oxide electrochemical capacitors  

SciTech Connect (OSTI)

Porous nickel oxide films were prepared by electrochemically precipitating nickel hydroxide and heating the hydroxide in air at 300 C. The resulting nickel oxide films behave as an electrochemical capacitor with a specific capacitance of 59 F/g electrode material. These nickel oxide films maintain high utilization at high rates of discharge (i.e., high power density) and have excellent cycle life. Porous cobalt oxide films were also synthesized. Although the specific capacitances of these films are approximately one-fifth that of the nickel oxide films, the results demonstrate the versatility of fabricating a wide range of porous metal oxide films using this electrochemical route for use in capacitor applications. Electrochemical capacitors have generated wide interest in recent years for use in high power applications (e.g., in a hybrid electric vehicle, where they are expected to work in conjunction with a conventional battery).

Srinivasan, V.; Weidner, J.W. [Univ. of South Carolina, Columbia, SC (United States). Dept. of Chemical Engineering

1997-08-01T23:59:59.000Z

465

Method for dialysis on microchips using thin porous polymer membrane  

DOE Patents [OSTI]

Laser-induced phase-separation polymerization of a porous acrylate polymer is used for in-situ fabrication of dialysis membranes inside glass microchannels. A shaped 355 nm laser beam is used to produce a porous polymer membrane with a thickness of about 15 .mu.m, which bonds to the glass microchannel and forms a semi-permeable membrane. Differential permeation through a membrane formed with pentaerythritol triacrylate was observed and quantified by comparing the response of the membrane to fluorescein and fluorescently tagging 200 nm latex microspheres. Differential permeation was observed and quantified by comparing the response to rhodamine 560 and lactalbumin protein in a membrane formed with SPE-methylene bisacrylamide. The porous membranes illustrate the capability for the present technique to integrate sample cleanup into chip-based analysis systems.

Singh, Anup K. (San Francisco, CA); Kirby, Brian J. (San Francisco, CA); Shepodd, Timothy J. (Livermore, CA)

2009-05-19T23:59:59.000Z

466

Dialysis on microchips using thin porous polymer membranes  

DOE Patents [OSTI]

Laser-induced phase-separation polymerization of a porous acrylate polymer is used for in-situ fabrication of dialysis membranes inside glass microchannels. A shaped 355 nm laser beam is used to produce a porous polymer membrane with a thickness of about 15 .mu.m, which bonds to the glass microchannel and form a semi-permeable membrane. Differential permeation through a membrane formed with pentaerythritol triacrylate was observed and quantified by comparing the response of the membrane to fluorescein and fluorescently tagging 200 nm latex microspheres. Differential permeation was observed and quantified by comparing the response to rhodamine 560 and lactalbumin protein in a membrane formed with SPE-methylene bisacrylamide. The porous membranes illustrate the capability for the present technique to integrate sample cleanup into chip-based analysis systems.

Singh, Anup K. (San Francisco, CA); Kirby, Brian J. (San Francisco, CA); Shepodd, Timothy J. (Livermore, CA)

2007-09-04T23:59:59.000Z

467

Anisotropy of flow in stochastically generated porous media  

E-Print Network [OSTI]

Models of porous media are often applied to relatively small systems, which leads not only to system-size-dependent results, but also to phenomena that would be absent in larger systems. Here we investigate one such finite-size effect: anisotropy of the permeability tensor. We show that a non-zero angle between the external body force and macroscopic flux vector exists in three-dimensional periodic models of sizes commonly used in computer simulations and propose a criterion, based on the system size to the grain size ratio, for this phenomenon to be relevant or negligible. The finite-size anisotropy of the porous matrix induces a pressure gradient perpendicular to the axis of a porous duct and we analyze how this effect scales with the system and grain sizes.

Matyka, Maciej; Go?embiewski, Jaros?aw; Kostur, Marcin; Januszewski, Micha?

2013-01-01T23:59:59.000Z

468

Selective Extraction of Uranium from Liquid or Supercritical Carbon Dioxide  

SciTech Connect (OSTI)

Current liquid-liquid extraction processes used in recycling irradiated nuclear fuel rely on (1) strong nitric acid to dissolve uranium oxide fuel, and (2) the use of aliphatic hydrocarbons as a diluent in formulating the solvent used to extract uranium. The nitric acid dissolution process is not selective. It dissolves virtually the entire fuel meat which complicates the uranium extraction process. In addition, a solvent washing process is used to remove TBP degradation products, which adds complexity to the recycling plant and increases the overall plant footprint and cost. A liquid or supercritical carbon dioxide (l/sc -CO2) system was designed to mitigate these problems. Indeed, TBP nitric acid complexes are highly soluble in l/sc -CO2 and are capable of extracting uranium directly from UO2, UO3 and U3O8 powders. This eliminates the need for total acid dissolution of the irradiated fuel. Furthermore, since CO2 is easily recycled by evaporation at room temperature and pressure, it eliminates the complex solvent washing process. In this report, we demonstrate: (1) A reprocessing scheme starting with the selective extraction of uranium from solid uranium oxides into a TBP-HNO3 loaded Sc-CO2 phase, (2) Back extraction of uranium into an aqueous phase, and (3) Conversion of recovered purified uranium into uranium oxide. The purified uranium product from step 3 can be disposed of as low level waste, or mixed with enriched uranium for use in a reactor for another fuel cycle. After an introduction on the concept and properties of supercritical fluids, we first report the characterization of the different oxides used for this project. Our extraction system and our online monitoring capability using UV-Vis absorbance spectroscopy directly in sc-CO2 is then presented. Next, the uranium extraction efficiencies and kinetics is demonstrated for different oxides and under different physical and chemical conditions: l/sc -CO2 pressure and temperature, TBP/HNO3 complex used, reductant or complexant used for selectivity, and ionic liquids used as supportive media. To complete the extraction and recovery cycle, we then demonstrate uranium back extraction from the TBP loaded sc-CO2 phase into an aqueous phase and the characterization of the uranium complex formed at the end of this process. Another aspect of this project was to limit proliferation risks by either co-extracting uranium and plutonium, or by leaving plutonium behind by selectively extracting uranium. We report that the former is easily achieved, since plutonium is in the tetravalent or hexavalent oxidation state in the oxidizing environment created by the TBP-nitric acid complex, and is therefore co-extracted. The latter is more challenging, as a reductant or complexant to plutonium has to be used to selectively extract uranium. After undertaking experiments on different reducing or complexing systems (e.g., AcetoHydroxamic Acid (AHA), Fe(II), ascorbic acid), oxalic acid was chosen as it can complex tetravalent actinides (Pu, Np, Th) in the aqueous phase while allowing the extraction of hexavalent uranium in the sc-CO2 phase. Finally, we show results using an alternative media to commonly used aqueous phases: ionic liquids. We show the dissolution of uranium in ionic liquids and its extraction using sc-CO2 with and without the presence of AHA. The possible separation of trivalent actinides from uranium is also demonstrated in ionic liquids using neodymium as a surrogate and diglycolamides as the extractant.

Farawila, Anne F.; O'Hara, Matthew J.; Wai, Chien M.; Taylor, Harry Z.; Liao, Yu-Jung

2012-07-31T23:59:59.000Z

469

Low-frequency dilatational wave propagation through unsaturated porous media containing two immiscible fluids  

E-Print Network [OSTI]

of elastic waves in unconsolidated unsaturated granularfrequency in both unconsolidated and consolidated materialsboth consolidated and unconsolidated porous media, and the

Lo, W.-C.

2009-01-01T23:59:59.000Z

470

Transport in Porous Media 52: 185211, 2003. 2003 Kluwer Academic Publishers. Printed in the Netherlands.  

E-Print Network [OSTI]

in the Netherlands. 185 Wettability Alteration to Intermediate Gas-Wetting in Porous Media at Elevated Temperatures

Firoozabadi, Abbas

471

Transport in Porous Media 57: 125152, 2004. 2004 Kluwer Academic Publishers. Printed in the Netherlands.  

E-Print Network [OSTI]

in the Netherlands. 125 Relative Permeabilities for Strictly Hyperbolic Models of Three-Phase Flow in Porous Media

Patzek, Tadeusz W.

472

Ultrasonic liquid level detector  

DOE Patents [OSTI]

An ultrasonic liquid level detector for use within a shielded container, the detector being tubular in shape with a chamber at its lower end into which liquid from in the container may enter and exit, the chamber having an ultrasonic transmitter and receiver in its top wall and a reflector plate or target as its bottom wall whereby when liquid fills the chamber a complete medium is then present through which an ultrasonic wave may be transmitted and reflected from the target thus signaling that the liquid is at chamber level.

Kotz, Dennis M. (North Augusta, SC); Hinz, William R. (Augusta, GA)

2010-09-28T23:59:59.000Z

473

Liquid Metal Transformers  

E-Print Network [OSTI]

The room temperature liquid metal is quickly emerging as an important functional material in a variety of areas like chip cooling, 3D printing or printed electronics etc. With diverse capabilities in electrical, thermal and flowing behaviors, such fluid owns many intriguing properties that had never been anticipated before. Here, we show a group of unconventional phenomena occurring on the liquid metal objects. Through applying electrical field on the liquid metals immersed in water, a series of complex transformation behaviors such as self-assembling of a sheet of liquid metal film into a single sphere, quick mergences of separate metal droplets, controlled self-rotation and planar locomotion of liquid metal objects can be realized. Meanwhile, it was also found that two accompanying water vortexes were induced and reliably swirled near the rotating liquid metal sphere. Further, effects of the shape, size, voltage, orientation and geometries of the electrodes to control the liquid metal transformers were clarified. Such events are hard to achieve otherwise on rigid metal or conventional liquid spheres. This finding has both fundamental and practical significances which suggest a generalized way of making smart soft machine, collecting discrete metal fluids, as well as flexibly manipulating liquid metal objects including accompanying devices.

Lei Sheng; Jie Zhang; Jing Liu

2014-01-30T23:59:59.000Z

474

Liquid Crystal Optofluidics  

SciTech Connect (OSTI)

By employing anisotropic fluids and namely liquid crystals, fluid flow becomes an additional degree of freedom in designing optofluidic devices. In this paper, we demonstrate optofluidic liquid crystal devices based on the direct flow of nematic liquid crystals in microfluidic channels. Contrary to previous reports, in the present embodiment we employ the effective phase delay acquired by light travelling through flowing liquid crystal, without analysing the polarisation state of the transmitted light. With this method, we demonstrate the variation in the diffraction pattern of an array of microfluidic channels acting as a grating. We also discuss our recent activities in integrating mechanical oscillators for on-chip peristaltic pumping.

Vasdekis, Andreas E.; Cuennet, J. G.; Psaltis, D.

2012-10-11T23:59:59.000Z

475

(Ionization in liquids)  

SciTech Connect (OSTI)

This document describes charge transport following ionization of model liquids and how this process may be important in carcinogenesis. 15 refs., 2 figs., 4 tabs. (MHB)

Not Available

1991-01-01T23:59:59.000Z

476

Water Quality and Hydrologic Performance of a Porous Asphalt Pavement as a Storm-Water  

E-Print Network [OSTI]

examined the functionality of a porous pavement storm-water management system in coastal New Hampshire headings: Stormwater management; Runoff; Porous media; Pavements; Cold regions; Best Management Practice; Water quality; Water treatment. Author keywords: Storm-water management; Runoff; Porous pavements; Cold

477

Porous silicon with embedded tritium as a stand-alone prime power source for optoelectronic applications  

DOE Patents [OSTI]

Disclosed is an illumination source comprising a porous silicon having a source of electrons on the surface and/or interstices thereof having a total porosity in the range of from about 50 v/o to about 90 v/o. Also disclosed are a tritiated porous silicon and a photovoltaic device and an illumination source of tritiated porous silicon. 1 fig.

Tam, S.W.

1997-02-25T23:59:59.000Z

478

Porous silicon with embedded tritium as a stand-alone prime power source for optoelectronic applications  

DOE Patents [OSTI]

An illumination source comprising a porous silicon having a source of electrons on the surface and/or interticies thereof having a total porosity in the range of from about 50 v/o to about 90 v/o. Also disclosed are a tritiated porous silicon and a photovoltaic device and an illumination source of tritiated porous silicon.

Tam, Shiu-Wing (Downers Grove, IL)

1997-01-01T23:59:59.000Z

479

Porous silicon with embedded tritium as a stand-alone prime power source for optoelectronic applications  

DOE Patents [OSTI]

An illumination source comprising a porous silicon having a source of electrons on the surface and/or interticies thereof having a total porosity in the range of from about 50 v/o to about 90 v/o. Also disclosed are a tritiated porous silicon and a photovoltaic device and an illumination source of tritiated porous silicon.

Tam, Shiu-Wing (Downers Grove, IL)

1998-01-01T23:59:59.000Z

480

Porous silicon with embedded tritium as a stand-alone prime power source for optoelectronic applications  

DOE Patents [OSTI]

An illumination source is disclosed comprising a porous silicon having a source of electrons on the surface and/or interstices thereof having a total porosity in the range of from about 50 v/o to about 90 v/o. Also disclosed are a tritiated porous silicon and a photovoltaic device and an illumination source of tritiated porous silicon. 1 fig.

Tam, S.W.

1998-06-16T23:59:59.000Z

Note: This page contains sample records for the topic "ionic liquid porous" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


481

On the Effect of Porous Layers on Melting Heat Transfer in an Enclosure  

E-Print Network [OSTI]

On the Effect of Porous Layers on Melting Heat Transfer in an Enclosure E. A. Ellinger* and C. To enhance heat transfer, the porous layers are located in regions where the melting rates for a pure the porous layer and the pure fluid layer cause strong variations in heat transfer, melt convection

Beckermann, Christoph

482

DYNAMICS OF FREE SURFACES IN RANDOM POROUS MEDIA DANIEL M. TARTAKOVSKY AND C. L. WINTER  

E-Print Network [OSTI]

media to be concrete. Predicting flow through natural porous media is complicated by their high degreeDYNAMICS OF FREE SURFACES IN RANDOM POROUS MEDIA DANIEL M. TARTAKOVSKY AND C. L. WINTER SIAM J­1876 Abstract. We consider free surface flow in random porous media by treating hydraulic conduc- tivity

Tartakovsky, Daniel M.

483

A model for reactive porous transport during re-wetting of hardened concrete  

E-Print Network [OSTI]

A model for reactive porous transport during re-wetting of hardened concrete Michael Chapwanya residing in the porous concrete matrix. The main hypothesis in this model is that the reaction product hydration; Porous media; Reaction-diffusion equations; Vari- able porosity. 1. Introduction Concrete

Stockie, John

484

Asymptotical Computations for a Model of Flow in Saturated Porous Media  

E-Print Network [OSTI]

a variably saturated porous medium with exponential diffusivity, such as soil, rock or concrete is given by uAsymptotical Computations for a Model of Flow in Saturated Porous Media P. Amodio a , C.J. Budd b for an implicit second order ordinary differential equation which arises in models of flow in saturated porous

Weinmüller, Ewa B.

485

Imaging biofilm architecture within porous media using synchrotron-based X-ray computed microtomography  

E-Print Network [OSTI]

Imaging biofilm architecture within porous media using synchrotron-based X-ray computed. Wildenschild (2011), Imaging biofilm architecture within porous media using synchrotron-based X-ray computed synchrotron-based X-ray computed microtomography (CMT) has been developed. Imaging biofilms in porous media

Wildenschild, Dorthe

486

Electrochimica Acta 52 (2007) 43174324 Porous current collectors for passive direct methanol fuel cells  

E-Print Network [OSTI]

Electrochimica Acta 52 (2007) 4317­4324 Porous current collectors for passive direct methanol fuel methanol fuel cell (DMFC) with its cathode current collector made of porous metal foam was investigated that the passive DMFC having the porous current collector yielded much higher and much more stable performance than

Zhao, Tianshou

2007-01-01T23:59:59.000Z

487

Fabrication and testing of oxidized porous silicon field emitter strips  

E-Print Network [OSTI]

mechanism. Formation by Local Dissolution of Silicon Unagami proposed [29] that the formation of porous silicon occurs due to the dissolution of silicon at places restricted by a surface porous film and silicic acid formed during the dissolution reaction... anodized in the presence of HF electmlyte. The silicon wafer divides the electrochemical cell into front and rear half cells. Each of the cells was filled with the electrolyte which is a mixture of 1. 5:1 hydroflouric acid and ethanol. Ethanol is used...

Madduri, Vasanta Bhanu

1992-01-01T23:59:59.000Z

488

Absorption of sound in liquids and liquid mixtures  

E-Print Network [OSTI]

ABSORPTION OF SOUND IN LIQUIDS AND LIQUID MIXTURES A Thesis Raiq S. causa Approved as to style and content by: (Chairman of Committee) January 1955 L1BRARY A 4 M COLLEOE OF IEXAS ADSORPTION OF SOfP@ LIQUIDS AND LIQUID NIXTURES A Thesis... Introduction to the Problem Experimental Methods and Procedures Results Discussion of Results Acknowledgements Bib 1 io graphy 22 4I 42 Introduction to the Problem The study of sound absorption in liquids and liquid mixtures is of considerable...

Musa, Raiq S

2012-06-07T23:59:59.000Z

489

Carbon monoxide absorbing liquid  

SciTech Connect (OSTI)

The present disclosure is directed to a carbon monoxide absorbing liquid containing a cuprous ion, hydrochloric acid and titanum trichloride. Titanium trichloride is effective in increasing the carbon monoxide absorption quantity. Furthermore, titanium trichloride remarkably increases the oxygen resistance. Therefore, this absorbing liquid can be used continuously and for a long time.

Arikawa, Y.; Horigome, S.; Kanehori, K.; Katsumoto, M.

1981-07-07T23:59:59.000Z

490

INEEL Liquid Effluent Inventory  

SciTech Connect (OSTI)

The INEEL contractors and their associated facilities are required to identify all liquid effluent discharges that may impact the environment at the INEEL. This liquid effluent information is then placed in the Liquid Effluent Inventory (LEI) database, which is maintained by the INEEL prime contractor. The purpose of the LEI is to identify and maintain a current listing of all liquid effluent discharge points and to identify which discharges are subject to federal, state, or local permitting or reporting requirements and DOE order requirements. Initial characterization, which represents most of the INEEL liquid effluents, has been performed, and additional characterization may be required in the future to meet regulations. LEI information is made available to persons responsible for or concerned with INEEL compliance with liquid effluent permitting or reporting requirements, such as the National Pollutant Discharge Elimination System, Wastewater Land Application, Storm Water Pollution Prevention, Spill Prevention Control and Countermeasures, and Industrial Wastewater Pretreatment. The State of Idaho Environmental Oversight and Monitoring Program also needs the information for tracking liquid effluent discharges at the INEEL. The information provides a baseline from which future liquid discharges can be identified, characterized, and regulated, if appropriate. The review covered new and removed buildings/structures, buildings/structures which most likely had new, relocated, or removed LEI discharge points, and at least 10% of the remaining discharge points.

Major, C.A.

1997-06-01T23:59:59.000Z

491

Liquid heat capacity lasers  

DOE Patents [OSTI]

The heat capacity laser concept is extended to systems in which the heat capacity lasing media is a liquid. The laser active liquid is circulated from a reservoir (where the bulk of the media and hence waste heat resides) through a channel so configured for both optical pumping of the media for gain and for light amplification from the resulting gain.

Comaskey, Brian J. (Walnut Creek, CA); Scheibner, Karl F. (Tracy, CA); Ault, Earl R. (Livermore, CA)

2007-05-01T23:59:59.000Z

492

Acoustic wave propagation in two-phase heterogeneous porous media  

E-Print Network [OSTI]

The propagation of an acoustic wave through two-phase porous media with spatial variation in porosity is studied. The evolutionary wave equation is derived, and the propagation of an acoustic wave is numerically analyzed in application to marine sediments with various physical parameters.

J. I. Osypik; N. I. Pushkina; Ya. M. Zhileikin

2015-03-19T23:59:59.000Z

493

Numerical simulation of transpiration cooling through porous , T. Gotzen1  

E-Print Network [OSTI]

55, 52056 Aachen SUMMARY Transpiration cooling using ceramic matrix composite (CMC) materials to facilitate such numerical simulations for a carbon/carbon material mounted in the side wall of a hot gasNumerical simulation of transpiration cooling through porous material W. Dahmen1 , T. Gotzen1 and S

494

ORIGINAL PAPER Conditional simulations of wateroil flow in heterogeneous porous  

E-Print Network [OSTI]

water standards. Thus, a small amount of NAPL can contaminate large volumes of groundwater over a long period of time. Therefore, it is very important to understand the processes associated with contaminant is a complicated mixture of hydrocarbon fluids, brine, porous rock and fractures. The structure of the void space

Lu, Zhiming

495

Elastic properties of saturated porous rocks with aligned fractures  

E-Print Network [OSTI]

Several treatments of the porous media with aligned fractures have been ...... a function of background porosity /p for water-satu- rated rock (Kf = 2.25 ? 109 Pa). .... that are in hydraulic equilibrium with the fractures, the fluid will squeeze from ...

2003-12-02T23:59:59.000Z

496

Numerical simulation of fluid flow in porous/fractured media  

SciTech Connect (OSTI)

Theoretical models of fluid flow in porous/fractured media can help in the design of in situ fossil energy and mineral extraction technologies. Because of the complexity of these processes, numerical solutions are usually required. Sample calculations illustrate the capabilities of present day computer models.

Travis B.J.; Cook, T.L.

1981-01-01T23:59:59.000Z

497

Method for the preparation of ferrous low carbon porous material  

SciTech Connect (OSTI)

A method for preparing a porous metal article using a powder metallurgy forming process is provided which eliminates the conventional steps associated with removing residual carbon. The method uses a feedstock that includes a ferrous metal powder and a polycarbonate binder. The polycarbonate binder can be removed by thermal decomposition after the metal article is formed without leaving a carbon residue.

Miller, Curtis Jack

2014-05-27T23:59:59.000Z

498

High-strength porous carbon and its multifunctional applications  

DOE Patents [OSTI]

High-strength porous carbon and a method of its manufacture are described for multifunctional applications, such as ballistic protection, structural components, ultracapacitor electrodes, gas storage, and radiation shielding. The carbon is produced from a polymer precursor via carbonization, and optionally by surface activation and post-treatment.

Wojtowicz, Marek A; Rubenstein, Eric P; Serio, Michael A; Cosgrove, Joseph E

2013-12-31T23:59:59.000Z

499

Pyrolytic carbon electrodes Lithographically Defined Porous Carbon Electrodes**  

E-Print Network [OSTI]

to the intrinsic material properties of carbon, functionalized films can be produced through chemical modification fabrication method capable of producing large area (%100 s cm2 ) submicrometer porous carbon films. In our methodology. The palladium-modified electrodes exhibit a catalytic response for methanol oxidation

New Mexico, University of

500

Exponential decay in one-dimensional porous-thermo-elasticity  

E-Print Network [OSTI]

is the equilibrated stress, g is the equilibrated body force and q is the heat flux. The variables u" (BFM2003- 00309) of the Spanish Ministry of Science and Technology. Keywords: porous energy density is a positive definite form. Thus, the constitutive coefficients satisfy the conditions: µ

Politècnica de Catalunya, Universitat