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Sample records for waiver mtbe methyl

  1. Manipulation of the HIF–Vegf pathway rescues methyl tert-butyl ether (MTBE)-induced vascular lesions

    SciTech Connect (OSTI)

    Bonventre, Josephine A.; Kung, Tiffany S.; White, Lori A.; Cooper, Keith R.

    2013-12-15

    Methyl tert-butyl ether (MTBE) has been shown to be specifically anti-angiogenic in piscine and mammalian model systems at concentrations that appear non-toxic in other organ systems. The mechanism by which MTBE targets developing vascular structures is unknown. A global transcriptome analysis of zebrafish embryos developmentally exposed to 0.00625–5 mM MTBE suggested that hypoxia inducible factor (HIF)-regulated pathways were affected. HIF-driven angiogenesis via vascular endothelial growth factor (vegf) is essential to the developing vasculature of an embryo. Three rescue studies were designed to rescue MTBE-induced vascular lesions: pooled blood in the common cardinal vein (CCV), cranial hemorrhages (CH), and abnormal intersegmental vessels (ISV), and test the hypothesis that MTBE toxicity was HIF–Vegf dependent. First, zebrafish vegf-a over-expression via plasmid injection, resulted in significantly fewer CH and ISV lesions, 46 and 35% respectively, in embryos exposed to 10 mM MTBE. Then HIF degradation was inhibited in two ways. Chemical rescue by N-oxaloylglycine significantly reduced CCV and CH lesions by 30 and 32% in 10 mM exposed embryos, and ISV lesions were reduced 24% in 5 mM exposed zebrafish. Finally, a morpholino designed to knock-down ubiquitin associated von Hippel–Lindau protein, significantly reduced CCV lesions by 35% in 10 mM exposed embryos. In addition, expression of some angiogenesis related genes altered by MTBE exposure were rescued. These studies demonstrated that MTBE vascular toxicity is mediated by a down regulation of HIF–Vegf driven angiogenesis. The selective toxicity of MTBE toward developing vasculature makes it a potentially useful chemical in the designing of new drugs or in elucidating roles for specific angiogenic proteins in future studies of vascular development. - Highlights: • Global gene expression of MTBE exposed zebrafish suggested altered HIF1 signaling. • Over expression of zebrafish vegf-a rescues MTBE-induced vascular lesions. • Inhibiting PHD or knocking down VHL rescues MTBE-induced vascular lesions. • HIF1-Vegf driven angiogenesis is a target for MTBE vascular toxicity.

  2. Supply Impacts of an MTBE Ban

    Reports and Publications (EIA)

    2002-01-01

    This paper analyzes the supply impacts of removing methyl tertiary butyl ether (MTBE) from gasoline.

  3. MTBE Production Economics (Released in the STEO April 2001)

    Reports and Publications (EIA)

    2001-01-01

    The purpose of this analysis is to evaluate the causes of methyl tertiary butyl ether (MTBE) price increases in 2000.

  4. {gamma}-aminobutyric acid{sub A} (GABA{sub A}) receptor regulates ERK1/2 phosphorylation in rat hippocampus in high doses of Methyl Tert-Butyl Ether (MTBE)-induced impairment of spatial memory

    SciTech Connect (OSTI)

    Zheng Gang; Zhang Wenbin; Zhang Yun; Chen Yaoming; Liu Mingchao; Yao Ting; Yang Yanxia; Zhao Fang; Li Jingxia; Huang Chuanshu; Luo Wenjing Chen Jingyuan

    2009-04-15

    Experimental and occupational exposure to Methyl Tert-Butyl Ether (MTBE) has been reported to induce neurotoxicological and neurobehavioral effects, such as headache, nausea, dizziness, and disorientation, etc. However, the molecular mechanisms involved in MTBE-induced neurotoxicity are still not well understood. In the present study, we investigated the effects of MTBE on spatial memory and the expression and function of GABA{sub A} receptor in the hippocampus. Our results demonstrated that intraventricular injection of MTBE impaired the performance of the rats in a Morris water maze task, and significantly increased the expression of GABA{sub A} receptor {alpha}1 subunit in the hippocampus. The phosphorylation of ERK1/2 decreased after the MTBE injection. Furthermore, the decreased ability of learning and the reduction of phosphorylated ERK1/2 level of the MTBE-treated rats was partly reversed by bicuculline injected 30 min before the training. These results suggested that MTBE exposure could result in impaired spatial memory. GABA{sub A} receptor may play an important role in the MTBE-induced impairment of learning and memory by regulating the phosphorylation of ERK in the hippocampus.

  5. Status and Impacts of State MTBE Bans

    Reports and Publications (EIA)

    2003-01-01

    This paper describes legislation passed in 16 states banning or restricting the use of methyl tertiary butyl ether (MTBE) in gasoline. Analysis of the status and impact of these state MTBE bans is provided concerning the supply and potential price changes of gasoline.

  6. MTBE Production Economics

    Annual Energy Outlook [U.S. Energy Information Administration (EIA)]

    MTBE Production Economics Tancred C. M. Lidderdale Contents 1. Summary 2. MTBE Production ... End Notes 1. For an analysis of MTBE economics through 1999 refer to: U.S. ...

  7. Impact of Renewable Fuels Standard/MTBE Provisions of S. 517 Requested by Sens. Daschle & Murkowski

    Reports and Publications (EIA)

    2002-01-01

    Additional analysis of the impact of the Renewable Fuels Standard (RFS) and methyl tertiary butyl ether (MTBE) ban provisions of S. 517.

  8. Preparations for Meeting New York and Connecticut MTBE Bans

    Reports and Publications (EIA)

    2003-01-01

    In response to a Congressional request, the Energy Information Administration examined the progress being made to meet the bans on the use of methyl tertiary butyl ether (MTBE) being implemented in New York and Connecticut at the end of 2003.

  9. MTBE, Oxygenates, and Motor Gasoline

    Gasoline and Diesel Fuel Update (EIA)

    in water and does not biodegrade easily, there have been increasing detections of MTBE in ground waters and reservoirs. Because of the occurrence of MTBE in water supplies, ...

  10. Eliminating MTBE in Gasoline in 2006

    Reports and Publications (EIA)

    2006-01-01

    A review of the market implications resulting from the rapid change from methyl tertiary butyl ether (MTBE) to ethanol-blended reformulated gasoline (RFG) on the East Coast and in Texas. Strains in ethanol supply and distribution will increase the potential for price volatility in these regions this summer.

  11. Motor Gasoline Outlook and State MTBE Bans

    Reports and Publications (EIA)

    2003-01-01

    The U.S. is beginning the summer 2003 driving season with lower gasoline inventories and higher prices than last year. Recovery from this tight gasoline market could be made more difficult by impending state bans on the blending of methyl tertiary butyl ether (MTBE) into gasoline that are scheduled to begin later this year.

  12. MTBE, Oxygenates, and Motor Gasoline (Released in the STEO October 1999)

    Reports and Publications (EIA)

    1999-01-01

    The blending of methyl tertiary butyl ether (MTBE) into motor gasoline has increased dramatically since it was first produced 20 years ago. MTBE usage grew in the early 1980's in response to octane demand resulting initially from the phaseout of lead from gasoline and later from rising demand for premium gasoline. The oxygenated gasoline program stimulated an increase in MTBE production between 1990 and 1994. MTBE demand increased from 83,000 in 1990 to 161,000 barrels per day in 1994. The reformulated gasoline (RFG) program provided a further boost to oxygenate blending. The MTBE contained in motor gasoline increased to 269,000 barrels per day by 1997.

  13. Ecofuel plans MTBE plant in Italy

    SciTech Connect (OSTI)

    Alperowicz, N.

    1992-04-29

    Ecofuel (Milan), an ENI company, is evaluating construction of a new methyl tert-butyl ether (MTBE) plant in Italy, but has shelved plans for a world-scale MTBE unit in Mexico. The Italian unit is tied to ethylene expansion now under way. Later this year EniChem (Milan), a sister company, is due to complete construction of a 360,000-m.t./year cracker at Brindisi. The C{sub 4} stream available there and from the existing cracker at Priolo in Sicily should provide enough feed for a unit of up to 100,000 m.t./year of MTBE capacity. Some of the feedstock could also come from the Ravenna cracker.

  14. Impact of Renewable Fuels Standard/MTBE Provisions of S. 1766

    Reports and Publications (EIA)

    2002-01-01

    This service report addresses the Renewable Fuels Standard (RFS)/methyl tertiary butyl ether (MTBE) provisions of S. 1766. The 'S. 1766' Case reflects provisions of S. 1766 including a renewable fuels standard (RFS) reaching five billion gallons by 2012, a complete phase-out of MTBE within four years, and the option for states to waive the oxygen requirement for reformulated gasoline (RFG).

  15. Eliminating MTBE in Gasoline in 2006

    Gasoline and Diesel Fuel Update (EIA)

    in 2006. Companies' decisions to eliminate MTBE have been driven by State bans due to water contamination concerns, continuing liability exposure from adding MTBE to gasoline,...

  16. Oxygenates du`jour...MTBE? Ethanol? ETBE?

    SciTech Connect (OSTI)

    Wolfe, R.

    1995-12-31

    There are many different liquids that contain oxygen which could be blended into gasoline. The ones that have been tried and make the most sense are in the alcohol (R-OH) and ether (R-O-R) chemical family. The alcohols considered are: methanol (MeOH), ethanol (EtOH), tertiary butyl alcohol (TBA). The ethers are: methyl tertiary butyl ether (MTBE), ethyl tertiary butyl ether (ETBE), tertiary amyl methyl ether (TAME), tertiary amyl ethyl ether (TAEE), di-isopropyl ether (DIPE). Of the eight oxygenates listed above, the author describes the five that are still waiting for widespread marketing acceptance (methanol, TBA, TAME, TAEE, and DIPE). He then discusses the two most widely used oxygenates in the US, MTBE and ethanol, along with the up-and-coming ethanol ether, ETBE. Selected physical properties for all of these oxygenates can be found in Table 2 at the end of this paper. A figure shows a simplified alcohol/ether production flow chart for the oxygenates listed above and how they are interrelated.

  17. State Restrictions on Methyl Tertiary Butyl Ether (released in AEO2006)

    Reports and Publications (EIA)

    2006-01-01

    By the end of 2005, 25 states had barred, or passed laws banning, any more than trace levels of methyl tertiary butyl ether (MTBE) in their gasoline supplies, and legislation to ban MTBE was pending in 4 others. Some state laws address only MTBE; others also address ethers such as ethyl tertiary butyl ether (ETBE) and tertiary amyl methyl ether (TAME). Annual Energy Outlook 2006 assumes that all state MTBE bans prohibit the use of all ethers for gasoline blending.

  18. Motor Gasoline Outlook and State MTBE Bans

    Gasoline and Diesel Fuel Update (EIA)

    Several years ago MTBE was detected in water supplies scattered throughout the country, ... gasoline engines into surface and ground water. (For more information refer to the ...

  19. Effects of temperature and acidic pre-treatment on Fenton-driven oxidation of MTBE-spent granular activated carbon

    SciTech Connect (OSTI)

    Kan, E.; Huling, S.G.

    2009-03-01

    The effects of temperature and acidic pretreatment on Fenton-driven chemical oxidation of methyl tert-butyl ether (MTBE)-spent granular activated carbon (GAC, derived from bituminous coal) were investigated. Limiting factors in MTBE removal in GAC include the heterogeneous distribution of amended Fe, and slow intraparticle diffusive transport of MTBE and hydrogen peroxide (H{sub 2}O{sub 2}) into the 'reactive zone'. Acid pretreatment of GAC before Fe amendment altered the surface chemistry of the GAC, lowered the pH point of zero charge, and resulted in greater penetration and more uniform distribution of Fe in GAC. This led to a condition where Fe, MTBE, and H{sub 2}O{sub 2} coexisted over a larger volume of the GAC contributing to greater MTBE oxidation and removal. H{sub 2}O{sub 2} reaction and MTBE removal in GAC increased with temperature. Modeling H{sub 2}O{sub 2} transport and reaction in GAC indicated that H{sub 2}O{sub 2} penetration was inversely proportional with temperature and tortuosity, and occurred over a larger fraction of the total volume of small GAC particles (0.3 mm diameter) relative to large particles (1.2 mm diameter). Acidic pretreatment of GAC, Fe-amendment, elevated reaction temperature, and use of small GAC particles are operational parameters that improve Fenton-driven oxidation of MTBE in GAC. 29 refs., 6 figs., 1 tab.

  20. Location of MTBE and toluene in the channel system of the zeolite mordenite: Adsorption and host-guest interactions

    SciTech Connect (OSTI)

    Arletti, Rossella; Martucci, Annalisa; Alberti, Alberto; Pasti, Luisa; Nassi, Marianna; Bagatin, Roberto

    2012-10-15

    This paper reports a study of the location of Methyl Tertiary Butyl Ether (MTBE) and toluene molecules adsorbed in the pores of the organophylic zeolite mordenite from an aqueous solution. The presence of these organic molecules in the zeolite channels was revealed by structure refinement performed by the Rietveld method. About 3 molecules of MTBE and 3.6 molecules of toluene per unit cell were incorporated into the cavities of mordenite, representing 75% and 80% of the total absorption capacity of this zeolite. In both cases a water molecule was localized inside the side pocket of mordenite. The saturation capacity determined by the adsorption isotherms, obtained by batch experiments, and the weight loss given by thermogravimetric (TG) analyses were in very good agreement with these values. The interatomic distances obtained after the structural refinements suggest MTBE could be connected to the framework through a water molecule, while toluene could be bonded to framework oxygen atoms. The rapid and high adsorption of these hydrocarbons into the organophylic mordenite zeolite makes this cheap and environmental friendly material a suitable candidate for the removal of these pollutants from water. - graphical abstract: Location of MTBE (a) and toluene (b) in mordenite channels (projection along the [001] direction). Highlights: Black-Right-Pointing-Pointer We investigated the MTBE and toluene adsorption process into an organophilic zeolite mordenite. Black-Right-Pointing-Pointer The presence of MTBE and toluene in mordenite was determined by X-ray diffraction studies. Black-Right-Pointing-Pointer About 3 molecules of MTBE and 3.6 molecules of toluene per unit cell were incorporated into the zeolite cavities. Black-Right-Pointing-Pointer MTBE is connected to the framework through a water molecule. Black-Right-Pointing-Pointer Toluene is directly bonded to framework oxygen atoms.

  1. Iron optimization for Fenton-driven oxidation of MTBE-spent granular activated carbon

    SciTech Connect (OSTI)

    Scott G. Huling; Patrick K. Jones; Tony R. Lee

    2007-06-01

    Fenton-driven chemical oxidation of methyl tert-butyl ether (MTBE)-spent granular activated carbon (GAC) was accomplished through the addition of iron (Fe) and hydrogen peroxide (H{sub 2}O{sub 2}) (15.9 g/L; pH 3). The GAC used was URV, a bituminous-coal based carbon. The Fe concentration in GAC was incrementally varied (1020-25 660 mg/kg) by the addition of increasing concentrations of Fe solution (FeSO4{center_dot}7H{sub 2}O). MTBE degradation in Fe-amended GAC increased by an order of magnitude over Fe-unamended GAC and H{sub 2}O{sub 2} reaction was predominantly (99%) attributed to GAC-bound Fe within the porous structure of the GAC. Imaging and microanalysis of GAC particles indicated limited penetration of Fe into GAC. The optimal Fe concentration was 6710 mg/kg (1020 mg/kg background; 5690 mg/kg amended Fe) and resulted in the greatest MTBE removal and maximum Fe loading oxidation efficiency (MTBE oxidized (g)/Fe loaded to GAC(mg/Kg)). At lower Fe concentrations, the H{sub 2}O{sub 2} reaction was Fe limited. At higher Fe concentrations, the H{sub 2}O{sub 2} reaction was not entirely Fe limited, and reductions in GAC surface area, GAC pore volume, MTBE adsorption, and Fe loading oxidation efficiency were measured. Results are consistent with nonuniform distribution of Fe, pore blockage in H{sub 2}O{sub 2} transport, unavailable Fe, and limitations in H{sub 2}O{sub 2} diffusive transport, and emphasize the importance of optimal Fe loading. 22 refs., 6 figs., 2 tabs.

  2. Memorandum of Decision: Withdrawal of LED Lighting Waiver | Department...

    Office of Environmental Management (EM)

    LED Lighting Waiver Memorandum of Decision: Withdrawal of LED Lighting Waiver novemberdecisionwithdraw More Documents & Publications Nationwide Nonavailability Waiver: November...

  3. Unreasonable Cost Waivers | Department of Energy

    Office of Environmental Management (EM)

    Unreasonable Cost Waivers Unreasonable Cost Waivers unreasonablecost10-03-2012.pdf cnmidecision.pdf eaglepassdecision.pdf...

  4. De Minimis Waiver | Department of Energy

    Energy Savers [EERE]

    De Minimis Waiver De Minimis Waiver PDF icon eere_ba_de_minimis_public_interest_waiver More Documents & Publications De Minimis Public Interest Waiver: May 24, 2010 Nationwide Nonavailability Waiver: May 24, 2010 Nationwide Limited Public Interest Waiver for LED and HVAC Units

  5. NSRCC(A)WAIVER.pdf | Department of Energy

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

    NSRCC(A)WAIVER.pdf NSRCC(A)WAIVER.pdf PDF icon NSRCC(A)WAIVER.pdf More Documents & Publications Class Patent Waiver W(C)2008-004 NSRCMOU.pdf ClassWaiverNPUA-2.pdf...

  6. Current Test Procedure Waivers | Department of Energy

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

    Current Test Procedure Waivers Current Test Procedure Waivers The U.S. Department of Energy's (DOE) regulations for covered products permit a person to seek a waiver, or an interim waiver, from the test procedure requirements for covered appliances and commercial equipment if certain criteria are satisfied. Regulations applicable to test procedure waivers for appliances can be found at 10 CFR 430.27; those applicable to test procedure waivers for commercial equipment are at 10 CFR 431.401. This

  7. Patent Waivers Overview | Department of Energy

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

    Patent Waivers Overview Patent Waivers Overview A patent waiver refers to the government's waiver of rights in an invention arising from DOE-funded research so that private entities may expedite commercialization, quickly bringing their technologies from lab to market. There are three types of waivers: Advance, Identified, and Class patent waivers. Detailed Information As stated in 10 CFR 784.3 - Policy, Section 6 of Public Law 96-517 (the Bayh-Dole patent and trademark amendments of 1980), as

  8. Class Patent Waivers | Department of Energy

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

    waiver of domestic and foreign patent rights under agreement DE-FOA-0000792. March 1, ... waiver of domestic and foreign patent rights under agreement NA. February 12, 2013 ...

  9. Test Procedure Waivers | Department of Energy

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

    Appliance & Equipment Standards Rulemakings & Notices Test Procedure Waivers Test Procedure Waivers Products covered by standards change as manufacturers add new features to ...

  10. Nationwide Categorical Waiver | Department of Energy

    Energy Savers [EERE]

    Memorandum of Decision: Withdrawal of Waiver for Fluorescent Electronic Ballasts Capable of Dimming (Expired) Nationwide Limited Public Interest Waiver for LED Lighting and HVAC ...

  11. Shock tube ignition of ethanol, isobutene and MTBE: Experiments and modeling

    SciTech Connect (OSTI)

    Curran, H.J.; Dunphy, M.P.; Simmie, J.M.; Westbrook, C.K.; Pitz, W.J.

    1991-11-22

    The ignition of ethanol, isobutene and methyl tert-butyl ether (MTBE) has been studied experimentally in a shock tube and computationally with a detailed chemical kinetic model. Experimental results, consisting of ignition delay measurements, were obtained for a range of fuel/oxygen mixtures diluted in Argon, with temperatures varying over a range of 1100--1900 K. The numerical model consisted of a detailed kinetic reaction mechanism with more than 400 elementary reactions, chosen to describe reactions of each fuel and the smaller hydrocarbon and other species produced during their oxidation. The overall agreement between experimental and computed results was excellent, particularly for mixtures with greater than 0.3% fuel. The greatest sensitivity in the computed results was found to falloff parameters in the dissociation reactions of isobutene, ethane, methane, and ethyl and vinyl radicals, to the C{sub 3}H{sub 4} and C{sub 3}H{sub 5} reaction submechanisms in the model, and to the reactions in the H{sub 2}-O{sub 2}-Co submechanism.

  12. Advanced Patent Waivers | Department of Energy

    Energy Savers [EERE]

    Advanced Patent Waivers Advanced Patent Waivers March 31, 2014 Advance Patent Waiver W(A)2013-014 This is a request by W.R GRACE AND CO for a DOE waiver of domestic and foreign patent rights under agreement DE- EE0005991. March 31, 2014 Advance Patent Waiver W(A)2013-027 This is a request by ELECTRICORE INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005968 February 27, 2014 Advance Patent Waiver W(A)2013-031 This is a request by WESTINGHOUSE ELECTRIC COMPANY

  13. Separation Programs Releases and Waivers | Department of Energy

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

    Separation Programs Releases and Waivers Separation Programs Releases and Waivers PDF icon Attachment 7 - Separation Programs Releases and Waivers More Documents & Publications Self-Select Voluntary Separation Plan Template Workforce Restructuring Policy Involuntary Separation Program General Release and Waiver

  14. Closing_Language_Patent_Waiver_Grant_Cases.pdf | Department of...

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

    ClosingLanguagePatentWaiverGrantCases.pdf More Documents & Publications Identified Patent Waiver W(I)2009-004 Identified Patent Waiver W(I)2010-004 Advance Patent Waiver...

  15. Automobile proximity and indoor residential concentrations of BTEX and MTBE

    SciTech Connect (OSTI)

    Corsi, Dr. Richard; Morandi, Dr. Maria; Siegel, Dr. Jeffrey; Hun, Diana E

    2011-01-01

    Attached garages have been identified as important sources of indoor residential air pollution. However, the literature lacks information on how the proximity of cars to the living area affects indoor concentrations of gasoline-related compounds, and the origin of these pollutants. We analyzed data from the Relationships of Indoor, Outdoor, and Personal Air (RIOPA) study and evaluated 114 residences with cars in an attached garage, detached garage or carport, or without cars. Results indicate that homes with cars in attached garages were affected the most. Concentrations in homes with cars in detached garages and residences without cars were similar. The contribution from gasoline-related sources to indoor benzene and MTBE concentrations appeared to be dominated by car exhaust, or a combination of tailpipe and gasoline vapor emissions. Residing in a home with an attached garage could lead to benzene exposures ten times higher than exposures from commuting in heavy traffic.

  16. Nationwide Limited Public Interest Waiver for LED and HVAC Units |

    Energy Savers [EERE]

    Department of Energy Limited Public Interest Waiver for LED and HVAC Units Nationwide Limited Public Interest Waiver for LED and HVAC Units PDF icon eere_nationwide_public_interest_waiver More Documents & Publications Nationwide Nonavailability Waiver: February 11, 2010 (Please note, the waiver for LED traffic signals has been withdrawn effective December 1, 2010) Nationwide Nonavailability Waiver: November 5, 2010 Amended Nationwide Nonavailability Waiver: November 5, 2010

  17. Enforcement Policy on the Application of Waivers and on the Waiver Process

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

    | Department of Energy Policy on the Application of Waivers and on the Waiver Process Enforcement Policy on the Application of Waivers and on the Waiver Process December 23, 2010 In response to questions from manufacturers, on November 30, 2010, the Department of Energy sought views on the implementation of recently granted waivers establishing an alternative test procedure for large-capacity clothes washers. After reviewing the comments, relevant provisions of the Energy Policy and

  18. Identified Patent Waivers | Department of Energy

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

    DOE waiver of domestic and foreign patent rights under agreement DE-FE0000408. November ... DOE waiver of domestic and foreign patent rights under agreement DE-FE0000408. November ...

  19. Petition for Advance Waiver of Patent Rights | Department of...

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

    Advance Waiver of Patent Rights Petition for Advance Waiver of Patent Rights This the DOE form to petition for advance waiver of DOE patent rights under regulation 10 C.F.R. PART ...

  20. Petition for Identified Waiver of Patent Rights | Department...

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

    Identified Waiver of Patent Rights Petition for Identified Waiver of Patent Rights This the DOE form to petition for an identified waiver of DOE patent rights under regulation 10 ...

  1. ClassWaiver-PUA.pdf | Department of Energy

    Office of Environmental Management (EM)

    ClassWaiver-PUA.pdf ClassWaiver-PUA.pdf More Documents & Publications ClassWaiverNPUA-2.pdf EXHIBIT A: CRADA, WFO, PUA and NPUA Comparison Table, with suggested...

  2. (Expired) Nationwide Limited Public Interest Waiver for LED Lighting...

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

    (Expired) Nationwide Limited Public Interest Waiver for LED Lighting and HVAC Units: February 11, 2010 (Expired) Nationwide Limited Public Interest Waiver for LED Lighting and HVAC ...

  3. Class Patent Waiver W(C)2011-013

    Broader source: Energy.gov [DOE]

    This is a request by AGREEMENT FOR COMMERCIALIZING TECHNOLOGY (ACT) CLASS WAIVER for a DOE waiver of domestic and foreign patent rights under agreement N/A.

  4. Class Patent Waiver W(C)2011-009

    Broader source: Energy.gov [DOE]

    This is a request by WFO Class Waiver for a DOE waiver of domestic and foreign patent rights under agreement N/A.

  5. MemoAdvisoryAssistanceContractWaiver.pdf | Department of Energy

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

    MemoAdvisoryAssistanceContractWaiver.pdf More Documents & Publications ClosingLanguagePatentWaiverGrantCases.pdf UnSecMemoProjectManagementExpectationsFinancialAssistance23...

  6. DOE Issues Enforcement Guidance on Large-Capacity Clothes Washer Waivers and the Waiver Process

    Broader source: Energy.gov [DOE]

    Today, the Department of Energy issued enforcement guidance on the application of recently granted waivers for large-capacity clothes washers and announced steps to improve the waiver process – and...

  7. Microsoft Word - LBNL 53866_SPME-MTBE_Final_112103.doc

    Office of Scientific and Technical Information (OSTI)

    Determination of Methyl tert-Butyl Ether and tert-Butyl Alcohol in Water by Solid-Phase Microextraction/Head Space Analysis in Comparison to EPA Method 5030/8260B Keun-Chan Oh & William T. Stringfellow* Center for Environmental Biotechnology Lawrence Berkeley National Laboratory 1 Cyclotron Rd., MS70A-3317 Berkeley, CA 94720 September 9, 2003 *Corresponding author, phone: (510) 486-7093, fax: (510) 486-7152 email: wstringfellow@lbl.gov Oh & Stringfellow Page 2 of 28 Abstract Methyl

  8. Involuntary Separation Program General Release and Waiver | Department of

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

    Energy Program General Release and Waiver Involuntary Separation Program General Release and Waiver PDF icon Attachment 9 - Involuntary Separation Program General Release and Waiver More Documents & Publications Separation Programs Releases and Waivers Workforce Restructuring Policy AFGE Local 928

  9. Involuntary Separation Program General Release and Waiver

    Energy Savers [EERE]

    Involuntary Separation Program General Release and Waiver This Involuntary Separation Program General Release and Waiver ("Release") is entered into by and between ______________________ ("Employee") and _________ ("Employer") in connection with the Employer's determination that the Employee is being laid off from employment by ________. IN EXCHANGE FOR THE PROMISES SET FORTH BELOW, THE PARTIES AGREE AS FOLLOWS: 1. Valuable Consideration: In exchange for Employee

  10. Class_Waiver_NPUA-2.pdf | Department of Energy

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

    NPUA-2.pdf ClassWaiverNPUA-2.pdf ClassWaiverNPUA-2.pdf More Documents & Publications EXHIBIT A: CRADA, WFO, PUA and NPUA Comparison Table, with suggested changes...

  11. STATEMENT OF CONSIDERATIONS CLASS WAIVER OF THE GOVERNMENT'S

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

    AT DESIGNATED NON-PROPRIETARY USER FACILITIES: DOE WAIVER NO. W(C)-2008-003. This Class Waiver is intended to provide for the disposition of intellectual property rights and...

  12. Waiver of Preferential Right to Lease Highway Right of Way |...

    Open Energy Info (EERE)

    Waiver of Preferential Right to Lease Highway Right of Way Jump to: navigation, search OpenEI Reference LibraryAdd to library Reference: Waiver of Preferential Right to Lease...

  13. Advance Patent Waiver W(A)2002-023 | Department of Energy

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

    2-023 Advance Patent Waiver W(A)2002-023 PDF icon Advance Patent Waiver W(A)2002-023 More Documents & Publications Advance Patent Waiver W(A)2006-028 WA05056IBMWATSONRESEARCH...

  14. Class_Waiver_W_C-2003-001.pdf | Department of Energy

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

    sWaiverWC-2003-001.pdf More Documents & Publications ClassWaiverWC-2004-005.pdf WC2003001CLASSWAIVEROFPATENTRIGHTSFORTECHNOLOGYDEV.pdf ClassWaiverWC-2000-005.pdf...

  15. Class_Waiver_W_C-2002-003.pdf | Department of Energy

    Energy Savers [EERE]

    ClassWaiverWC-2002-003.pdf ClassWaiverWC-2002-003.pdf PDF icon ClassWaiverWC-2002-003.pdf More Documents & Publications WC2002003CLASSWAIVEROFTHEGOVERNMENTSUSAND...

  16. WC_1993_008_CLASS_WAIVER_ROCKETDYNE_DIVISION_ROCKWELL_INTERN.pdf |

    Energy Savers [EERE]

    Department of Energy 08_CLASS_WAIVER_ROCKETDYNE_DIVISION_ROCKWELL_INTERN.pdf WC_1993_008_CLASS_WAIVER_ROCKETDYNE_DIVISION_ROCKWELL_INTERN.pdf PDF icon WC_1993_008_CLASS_WAIVER_ROCKETDYNE_DIVISION_ROCKWELL_INTERN.pdf More Documents & Publications WC_1993_002_CRADA_CLASS_WAIVER_SOUTHERN_UNIVERSITY_RESEARCH_.pdf WC_1990_012_CLASS_WAIVER_of_Patent_Rights_in_Inventions_Made.pdf WA_1993_041_ROCKETDYNE_AND_LLNL_Waiver_of_the_Governments_U

  17. Advance Patent Waiver W(A)2011-062

    Broader source: Energy.gov [DOE]

    This is a request by ABENGOA SOLAR INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18038.

  18. Advance Patent Waiver W(A)2011-056

    Broader source: Energy.gov [DOE]

    This is a request by ABENGOA SOLAR INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18036.

  19. Advance Patent Waiver W(A)2011-063

    Broader source: Energy.gov [DOE]

    This is a request by ABENGOA SOLAR INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18156.

  20. Advance Patent Waiver W(A)2008-010

    Broader source: Energy.gov [DOE]

    This is a request by XANTREX TECHNOLOGY, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-07GO17043

  1. Advance Patent Waiver W(A)2007-021

    Broader source: Energy.gov [DOE]

    This is a request by SUN POWER CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-PS36-06GO96034

  2. Advance Patent Waiver W(A)2010-055

    Broader source: Energy.gov [DOE]

    This is a request by SUN POWER CORPORATIO for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0002066

  3. Advance Patent Waiver W(A)2006-032

    Broader source: Energy.gov [DOE]

    This is a request by HONEYWELL INTERNATIONAL, INC. for a DOE waiver of domestic and foreign patent rights under agreement UNKNOWN

  4. Advance Patent Waiver W(A)2012-003

    Broader source: Energy.gov [DOE]

    This is a request by CREE for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FOA-0000439.

  5. Advance Patent Waiver W(A)2005-043

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL ELECTRIC COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42451.

  6. Advance Patent Waiver W(A)2011-050

    Broader source: Energy.gov [DOE]

    This is a request by EMERSON ELECTRIC for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0004000.

  7. Advance Patent Waiver W(A)2005-004

    Broader source: Energy.gov [DOE]

    This is a request by ALSTO for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-03NT41986.

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  9. Advance Patent Waiver W(A)2012-024

    Broader source: Energy.gov [DOE]

    This is a request by SIEMENS ENERGY, INC. for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0005493.

  10. Advance Patent Waiver W(A)2010-061

    Broader source: Energy.gov [DOE]

    This is a request by PALTO ALTO RESEARCH CENTER, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0002765

  11. Advance Patent Waiver W(A)2010-066

    Broader source: Energy.gov [DOE]

    This is a request by A.O. SMITH CORP. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003985

  12. Identified Patent Waiver W(I)2008-009

    Broader source: Energy.gov [DOE]

    This is a request by SABIC INNOVATIVE PLASTICS for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-03GO13000

  13. Class Patent Waiver W(C)2010-005

    Broader source: Energy.gov [DOE]

    This is a request by REGIONAL INNOVATIVE CLUSTER INITIATIVE for a DOE waiver of domestic and foreign patent rights under agreement E-RIC FOA

  14. Identified Patent Waiver W(I)2011-011

    Broader source: Energy.gov [DOE]

    This is a request by ALSTOM POWER, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-01NT41223.

  15. Identified Patent Waiver W(I)2011-012

    Broader source: Energy.gov [DOE]

    This is a request by ALSTOM POWER, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-01NT41223.

  16. Patent Waiver W(I)2011-013

    Broader source: Energy.gov [DOE]

    This is a request by ALSTOM POWER, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-01NT41223.

  17. Advance Patent Waiver W(A)2008-015

    Broader source: Energy.gov [DOE]

    This is a request by BP SOLAR LTD. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-GO17049

  18. Identified Patent Waiver W(I)2008-006

    Broader source: Energy.gov [DOE]

    This is a request by CLAGHORN, RONALD for a DOE waiver of domestic and foreign patent rights under agreement DE-AC27-01RV14136

  19. Advance Patent Waiver W(A)2011-005

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES RESEARCH CENTER for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003954.

  20. Identified Patent Waiver W(I)2008-001

    Broader source: Energy.gov [DOE]

    This is a request by IMAGINEERING TECHNOLOGIES INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-AC07-94ID13223

  1. Advance Patent Waiver W(A)2008-017

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by UNITED TECHNOLOGIES CORP for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-07GO17030

  2. Class Patent Waiver W(C)2010-001

    Broader source: Energy.gov [DOE]

    This is a request by TECHNOLOGY DEVELOPMENT CORP. for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000042

  3. Advance Patent Waiver W(A)2009-019

    Broader source: Energy.gov [DOE]

    This is a request by DOW CORNING CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18068

  4. Advance Patent Waiver W(A)2009-011

    Broader source: Energy.gov [DOE]

    This is a request by BOEING COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18135

  5. Advance Patent Waiver W(A)2009-032

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL ATOMICS for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18145

  6. Identified Patent Waiver W(I)2010-003

    Broader source: Energy.gov [DOE]

    This is a request by UOP, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FG26-04NT42121

  7. Advance Patent Waiver W(A)2009-018

    Broader source: Energy.gov [DOE]

    This is a request by CATERPILLAR, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43277

  8. Class Patent Waiver W(C)2009-016

    Broader source: Energy.gov [DOE]

    This is a request by GEOTHERMAL TECHNOLOGIES PROGRAM for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-00000109

  9. Advance Patent Waiver W(A)2012-027

    Broader source: Energy.gov [DOE]

    This is a request by DAIMIER TRUCKS NORTH AMERICA for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0003348.

  10. Identified Patent Waiver W(I)2010-007

    Broader source: Energy.gov [DOE]

    This is a request by HONEYWELL INTERNATIONAL, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-AC04-94AL85000

  11. Advance Patent Waiver W(A)2012-029

    Broader source: Energy.gov [DOE]

    This is a request by ALCOA COMMERICAL WINDOWS, LLC for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0004012.

  12. Advance Patent Waiver W(A)2011-039

    Broader source: Energy.gov [DOE]

    This is a request by 3M COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18134.

  13. Advance Patent Waiver W(A)2008-022

    Broader source: Energy.gov [DOE]

    This is a request by ABENGOA BIOENERGY BIOMASS OF KANSAS, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC3607017028

  14. Advance Patent Waiver W(A)2012-019

    Broader source: Energy.gov [DOE]

    This is a request by GE ENERGY for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FE0007902.

  15. Advance Patent Waiver W(A)2012-018

    Broader source: Energy.gov [DOE]

    This is a request by GE ENERGY for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FE0007859.

  16. Advance Patent Waiver W(A)2011-064

    Broader source: Energy.gov [DOE]

    This is a request by DELPHI AUTOMOTIVE SYSTEMS, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005342.

  17. Advance Patent Waiver W(A)2009-048

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by GENERAL ELECTRIC COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT0005310

  18. Advance Patent Waiver W(A)2011-026

    Broader source: Energy.gov [DOE]

    This is a request by US SYNTHETIC CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003633.

  19. Advance Patent Waiver W(A)2007-014

    Broader source: Energy.gov [DOE]

    This is a request by DONALDSON COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-06NT42861

  20. Advance Patent Waiver W(A)2010-021

    Broader source: Energy.gov [DOE]

    This is a request by PHILIPS LUMILEDS for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003249

  1. Advance Patent Waiver W(A)2010-047

    Broader source: Energy.gov [DOE]

    This is a request by APPLIED MATERIALS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003331

  2. Class Patent Waiver W(C)2010-002

    Broader source: Energy.gov [DOE]

    This is a request by VEHICLE TECHNOLOGIES BROAD AGENCY for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000239

  3. Advance Patent Waiver W(A)2008-027

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by ALCOA, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO180278

  4. Advance Patent Waiver W(A)2011-059

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by CARLISLE CONSTRUCTION MATERIALS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005435.

  5. Advance Patent Waiver W(A)2010-020

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by HALOTECHNICS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18144

  6. Advance Patent Waiver W(A)2007-012

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by BOEING for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-06GO17052

  7. Advance Patent Waiver W(A)2011-030

    Broader source: Energy.gov [DOE]

    This is a request by EATON CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003911.

  8. Advance Patent Waiver W(A)2013-027

    Broader source: Energy.gov [DOE]

    This is a request by ELECTRICORE INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005968

  9. Advance Patent Waiver W(A)2012-025

    Broader source: Energy.gov [DOE]

    This is a request by EATON CORPORATION for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-OE0000592.

  10. Advance Patent Waiver W(A)2012-032

    Broader source: Energy.gov [DOE]

    This is a request by EATON CORPORATION for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0005665.

  11. Advance Patent Waiver W(A)2009-051

    Broader source: Energy.gov [DOE]

    This is a request by CATERPILLAR, INC. for a DOE waiver of domestic and foreign patent rights under agreement De-FC26-02AL67974

  12. Advance Patent Waiver W(A)2011-065

    Broader source: Energy.gov [DOE]

    This is a request by OWENS CORNING for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005338.

  13. Advance Patent Waiver W(A)2009-007

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES CORP for a DOE waiver of domestic and foreign patent rights under agreement DE-AC02-05CH11231

  14. Advance Patent Waiver W(A)2011-038

    Broader source: Energy.gov [DOE]

    This is a request by A123 SYSTEMS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0001187.

  15. Advance Patent Waiver W(A)2008-035

    Broader source: Energy.gov [DOE]

    This is a request by POET RESEARCH, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO88033

  16. Advance Patent Waiver W(A)2012-020

    Broader source: Energy.gov [DOE]

    This is a request by CLIPPER WINDPOWER LLC for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0005141.

  17. Advance Patent Waiver W(A)2010-034

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by LUMINATION, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003232

  18. Advance Patent Waiver W(A)2005-061

    Broader source: Energy.gov [DOE]

    This is a request by CATERPILLAR for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42412.

  19. Advance Patent Waiver W(A)2005-052

    Broader source: Energy.gov [DOE]

    This is a request by CATERPILLAR, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42423.

  20. Identified Patent Waiver W(I)2011-005

    Broader source: Energy.gov [DOE]

    This is a request by MICHAEL BROCKWELL for a DOE waiver of domestic and foreign patent rights under agreement DE-AC52-06NA25396.

  1. Advance Patent Waiver W(A)2006-019

    Broader source: Energy.gov [DOE]

    This is a request by NALCO CHEMICAL CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-06FT42721

  2. Advance Patent Waiver W(A)2008-014

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL MOTORS CORP for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-07GO17018

  3. Advance Patent Waiver W(A)2010-028

    Broader source: Energy.gov [DOE]

    This is a request by ARKEMA for a DOE waiver of domestic and foreign patent rights under agreement DE-PS36-08GO98009

  4. Identified Patent Waiver W(I)2009-001

    Broader source: Energy.gov [DOE]

    This is a request by DUSAN RADOSAVLJEVIC for a DOE waiver of domestic and foreign patent rights under agreement DE-AC07-05ID14516

  5. Class Patent Waiver W(C)2011-004

    Broader source: Energy.gov [DOE]

    This is a request by PHOTOVOLTAIC (PV) MANUFACTURING for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000259.

  6. Advance Patent Waiver W(A)2010-049

    Broader source: Energy.gov [DOE]

    This is a request by PRAXAIR, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43088

  7. IIdentified Patent Waiver W(I)2008-003

    Broader source: Energy.gov [DOE]

    This is a request by NORMANN, RANDY A. for a DOE waiver of domestic and foreign patent rights under agreement DE-AC04-94AL85000

  8. Advance Patent Waiver W(A)2005-040

    Broader source: Energy.gov [DOE]

    This is a request by CORNING INCORPORATED for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42461.

  9. Advance Patent Waiver W(A)2010-024

    Broader source: Energy.gov [DOE]

    This is a request by EASTMAN CHEMICAL COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42469

  10. Advance Patent Waiver W(A)2011-049

    Broader source: Energy.gov [DOE]

    This is a request by DOW CHEMICAL COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003916.

  11. Advance Patent Waiver W(A)2012-016

    Broader source: Energy.gov [DOE]

    This is a request by LINDE, INC. for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FE0007453.

  12. Advance Patent Waiver W(A)2012-015

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL ELECTRIC GLOBAL REARCH for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FE0005859.

  13. Advance Patent Waiver W(A)2005-048

    Broader source: Energy.gov [DOE]

    This is a request by IBM BLUEGENE/P DESIGN, PHASE III for a DOE waiver of domestic and foreign patent rights under agreement W-7405-ENG-48.

  14. Class Patent Waiver W(C)2009-008

    Broader source: Energy.gov [DOE]

    This is a request by ARPA ENERGY for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA0000065

  15. Advance Patent Waiver W(A)2009-028

    Broader source: Energy.gov [DOE]

    This is a request by ARKEMA for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT01582

  16. Advance Patent Waiver W(A)2005-062

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42626.

  17. Advance Patent Waiver W(A)2009-061

    Broader source: Energy.gov [DOE]

    This is a request by PPG INDUSTRIES for a DOE waiver of domestic and foreign patent rights under agreement DE-NT0003894

  18. Advance Patent Waiver W(A)2009-064

    Broader source: Energy.gov [DOE]

    This is a request by ROLLS ROYCE FUEL SYSTEMS for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0000303

  19. Advance Patent Waiver W(A)2009-054

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES RESEARCH for a DOE waiver of domestic and foreign patent rights under agreement DE-PS36-08GO98010

  20. Advance Patent Waiver W(A)2009-010

    Broader source: Energy.gov [DOE]

    This is a request by SCHLUMBERGER TECHNOLOGY CORP for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18184

  1. Advance Patent Waiver W(A)2008-036

    Broader source: Energy.gov [DOE]

    This is a request by LIGNOL INNOVATIONS, LTD. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18047

  2. Advance Patent Waiver W(A)2009-044

    Broader source: Energy.gov [DOE]

    This is a request by FORD MOTOR COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-09GO19002

  3. Advance Patent Waiver W(A)2008-046

    Broader source: Energy.gov [DOE]

    This is a request by EATON CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18131

  4. Advance Patent Waiver W(A)2010-018

    Broader source: Energy.gov [DOE]

    This is a request by BOEING COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18055

  5. Advance Patent Waiver W(A)2011-031

    Broader source: Energy.gov [DOE]

    This is a request by PARKER HANNIFIN CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0005508.

  6. Advance Patent Waiver W(A)2010-035

    Broader source: Energy.gov [DOE]

    This is a request by GE GLOBAL RESEARCH for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003251

  7. Class Patent Waiver W(C)2008-008

    Broader source: Energy.gov [DOE]

    This is a request by University of Chicago for a DOE waiver of domestic and foreign patent rights under agreement DE-AC02-06CH11357

  8. Identified Patent Waiver W(I)2008-011

    Broader source: Energy.gov [DOE]

    This is a request by ELTRON RESEARCH, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42469

  9. Advance Patent Waiver W(A)2008-002

    Broader source: Energy.gov [DOE]

    This is a request by FORD MOTOR COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43276

  10. Advance Patent Waiver W(A)2005-036

    Broader source: Energy.gov [DOE]

    This is a request by POVAIR CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-02AL67627.

  11. Advance Patent Waiver W(A)2010-017

    Broader source: Energy.gov [DOE]

    This is a request by FORD MOTOR COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18128

  12. Advance Patent Waiver W(A)2009-025

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL ELECTRIC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT05868

  13. Advance Patent Waiver W(A)2011-036

    Broader source: Energy.gov [DOE]

    This is a request by HONEYWELL LABORATORIES for a DOE waiver of domestic and foreign patent rights under agreement DE-OE0000544.

  14. Advance Patent Waiver W(A)2011-008

    Broader source: Energy.gov [DOE]

    This is a request by CERAMATEC, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000395.

  15. Advance Patent Waiver W(A)2011-024

    Broader source: Energy.gov [DOE]

    This is a request by SCHWEITZER ENGINEERING LAB INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-OE0000538.

  16. Advance Patent Waiver W(A)2012-009

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by AE SOLAR for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0005340.

  17. Advance Patent Waiver W(A)2011-057

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by 3M COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003837.

  18. Advance Patent Waiver W(A)2011-027

    Broader source: Energy.gov [DOE]

    This is a request by VARIAN ASSOCIATES, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0004737.

  19. Advance Patent Waiver W(A)2010-048

    Broader source: Energy.gov [DOE]

    This is a request by ROBERT BOSCH, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43274

  20. Advance Patent Waiver W(A)2005-023

    Broader source: Energy.gov [DOE]

    This is a request by HEADWATER for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-04NT42448.

  1. Advance Patent Waiver W(A)2007-001

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by EASTMAN KODAK CO. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-06NT42933

  2. Identified Patent Waiver W(I)2008-008

    Broader source: Energy.gov [DOE]

    This is a request by SANDIA CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-AC04-94AL85000

  3. Advance Patent Waiver W(A)2011-040

    Broader source: Energy.gov [DOE]

    This is a request by SYPRIS ELECTRONICS for a DOE waiver of domestic and foreign patent rights under agreement DE-OE0000543.

  4. Advance Patent Waiver W(A)2005-049

    Broader source: Energy.gov [DOE]

    This is a request by AMERICAN AIR LIQUIDE for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-02NT41586.

  5. Advance Patent Waiver W(A)2011-002

    Broader source: Energy.gov [DOE]

    This is a request by APPLIED MATERIALS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003838.

  6. Identified Patent Waiver W(I)2011-001

    Broader source: Energy.gov [DOE]

    This is a request by UCHICAGO ARGONNE, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-AC02-06CH11357.

  7. Advance Patent Waiver W(A)2010-045

    Broader source: Energy.gov [DOE]

    This is a request by LUMMUS COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003457

  8. Title: Advance Patent Waiver W(A)2011-041

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL MOTOR for a DOE waiver of domestic and foreign patent rights under agreement DE-AC36-08GO28308.

  9. Class Patent Waiver W(C)2009-012

    Broader source: Energy.gov [DOE]

    This is a request by DEVELOPMENT OF ALGAL/ADVANCED BIOFUELS CONSORTIA for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000123

  10. Advance Patent Waiver W(A)2012-022

    Broader source: Energy.gov [DOE]

    This is a request by FORD MOTOR COMPANY for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FOA-0000421.

  11. Advance Patent Waiver W(A)2009-030

    Broader source: Energy.gov [DOE]

    This is a request by BALDOR ELECTRIC COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18132

  12. Advance Patent Waiver W(A)2011-037

    Broader source: Energy.gov [DOE]

    This is a request by DELPHI AUTOMOTIVE SYSTEMS, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000478.

  13. Advance Patent Waiver W(A)2011-010

    Broader source: Energy.gov [DOE]

    This is a request by CHEMTURA CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003986.

  14. Advance Patent Waiver W(A)2012-008

    Broader source: Energy.gov [DOE]

    This is a request by ROBERT BOSCH, LLC for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0003533.

  15. Advance Patent Waiver W(A)2012-002

    Broader source: Energy.gov [DOE]

    This is a request by NOVOZYMES NORTH AMERICA, INC. for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FE0007741.

  16. Identified Patent Waiver W(I)2011-003

    Broader source: Energy.gov [DOE]

    This is a request by RESONANT CAVITY APPARATUS for a DOE waiver of domestic and foreign patent rights under agreement DE-AC04-94AL85000.

  17. Advance Patent Waiver W(A)2011-058

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL ELECTRIC CO. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005143.

  18. Advance Patent Waiver W(A)2011-007

    Broader source: Energy.gov [DOE]

    This is a request by BAYER MATERIALSCIENCE LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0004571.

  19. Advance Patent Waiver W(A)2009-031

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES CORP for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-09GO19006

  20. Advance Patent Waiver W(A)2010-036

    Broader source: Energy.gov [DOE]

    This is a request by GE GLOBAL RESEARCH for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003251

  1. Advance Patent Waiver W(A)2010-029

    Broader source: Energy.gov [DOE]

    This is a request by OSRAM SYLVANI for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003241

  2. Identified Patent Waiver W(I)2010-008

    Broader source: Energy.gov [DOE]

    This is a request by BENEQ OY for a DOE waiver of domestic and foreign patent rights under agreement DE-AC36-08GO28308

  3. Advance Patent Waiver W(A)2007-015

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES CORP for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43055

  4. Advance Patent Waiver W(A)2012-007

    Broader source: Energy.gov [DOE]

    This is a request by NAVISTAR for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0003303.

  5. Advance Patent Waiver W(A)2011-046

    Broader source: Energy.gov [DOE]

    This is a request by ALSTOM GRID INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-OE0000551.

  6. Advance Patent Waiver W(A)2010-052

    Broader source: Energy.gov [DOE]

    This is a request by A123 SYSTEMS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE003513

  7. Advance Patent Waiver W(A)2005-058

    Broader source: Energy.gov [DOE]

    This is a request by ASTRONAUTICS CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-03NT1948.

  8. Advance Patent Waiver W(A)2008-005

    Broader source: Energy.gov [DOE]

    This is a request by AMERICAN SUPERCONDUCTOR CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43243

  9. Advance Patent Waiver W(A)2008-043

    Broader source: Energy.gov [DOE]

    This is a request by AMERICAN SUPERCONDUCTOR CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43240

  10. Advance Patent Waiver W(A)2005-027

    Broader source: Energy.gov [DOE]

    This is a request by WESTINGHOUSE ELECTRIC CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC07-05ID14636.

  11. Advance Patent Waiver W(A)2011-052

    Broader source: Energy.gov [DOE]

    This is a request by 3M COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000456.

  12. Advance Patent Waiver W(A)2009-052

    Broader source: Energy.gov [DOE]

    This is a request by 3M COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18027

  13. Advance Patent Waiver W(A)2006-014

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by PPG INDUSTRIES, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-04GO14044

  14. Advance Patent Waiver W(A)2009-049

    Broader source: Energy.gov [DOE]

    This is a request by SPX COOLING TECHNOLOGIESS for a DOE waiver of domestic and foreign patent rights under agreement DE-NT0005647

  15. Advance Patent Waiver W(A)2009-069

    Broader source: Energy.gov [DOE]

    This is a request by ENVIRON INTERNATIOAL CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000069

  16. Identified Patent Waiver W(I)2012-016

    Broader source: Energy.gov [DOE]

    This is a request by CERAMATEC, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0000408.

  17. Advance Patent Waiver W(A)2010-057

    Broader source: Energy.gov [DOE]

    This is a request by HONEYWELL INTERNATIONAL, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003840

  18. Advance Patent Waiver W(A)2012-013

    Broader source: Energy.gov [DOE]

    This is a request by BAKER HUGHES OILFIELD OPERATIONS, INC. for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0005505.

  19. Advance Patent Waiver W(A)2009-009

    Broader source: Energy.gov [DOE]

    This is a request by BAKER HUGHES for a DOE waiver of domestic and foreign patent rights under agreement DE-FG08-GO18186

  20. Advance Patent Waiver W(A)2008-011

    Broader source: Energy.gov [DOE]

    This is a request by DSM lnnovation, Inc. for a DOE waiver of domestic and foreign patent rights under agreement DE-PS36-06GO97034

  1. Advance Patent Waiver W(A)2010-007

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by 3M COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000650

  2. Advance Patent Waiver W(A)2005-016

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by BAKER HUGHES INTERNATIONAL for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT15488.

  3. Advance Patent Waiver W(A)2011-012

    Broader source: Energy.gov [DOE]

    This is a request by CAMBRIOS TECHNOLOGIES CORP. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003254.

  4. Advance Patent Waiver W(A)2008-044

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by ALSTOM POWER, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43095

  5. Advance Patent Waiver W(A)2009-005

    Broader source: Energy.gov [DOE]

    This is a request by CONOCO PHILIPS for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT0006553

  6. Advance Patent Waiver W(A)2013-011

    Broader source: Energy.gov [DOE]

    This is a request by DELPHI AUTOMOTIVE SYSTEMS, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005752.

  7. Advance Patent Waiver W(A)2008-032

    Broader source: Energy.gov [DOE]

    This is a request by CUMMINS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43279

  8. Advance Patent Waiver W(A)2010-030

    Broader source: Energy.gov [DOE]

    This is a request by RED ACQUISITION, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003364

  9. Advance Patent Waiver W(A)2009-059

    Broader source: Energy.gov [DOE]

    This is a request by PPG INDUSTRIES for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000167

  10. Advance Patent Waiver W(A)2011-021

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by CUMMINS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0004125.

  11. Advance Patent Waiver W(A)2010-054

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIE for a DOE waiver of domestic and foreign patent rights under agreement DE-NT003894

  12. Advance Patent Waiver W(A)2006-027

    Broader source: Energy.gov [DOE]

    This is a request by EASTMAN KODAK COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-06NT42864

  13. Advance Patent Waiver W(A)2011-014

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES RESEARCH CENTER for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003955.

  14. Advance Patent Waiver W(A)2010-041

    Broader source: Energy.gov [DOE]

    This is a request by W.L. GORE & ASSOCIATES for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000465

  15. Advance Patent Waiver W(A)2010-065

    Broader source: Energy.gov [DOE]

    This is a request by DRESSER WAUKESHA for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0004016

  16. Advance Patent Waiver W(A)2005-009

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by LUCENT TECHNOLOGIES, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FG02-04ER46118.

  17. Advance Patent Waiver W(A)2012-030

    Broader source: Energy.gov [DOE]

    This is a request by SRI INTERNATIONAL for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FE0000896.

  18. Advance Patent Waiver W(A)2008-021

    Broader source: Energy.gov [DOE]

    This is a request by CARGILL, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-07GO17055

  19. Advance Patent Waiver W(A)2011-069

    Broader source: Energy.gov [DOE]

    This is a request by NAVISTAR for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003303.

  20. Advance Patent Waiver W(A)2005-038

    Broader source: Energy.gov [DOE]

    This is a request by PHILLIPS ELECTRONIC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42342.

  1. Advance Patent Waiver W(A)2009-021

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by PHILIPS LUMILEDS for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT01583

  2. Class Patent Waiver W(C)2009-010

    Broader source: Energy.gov [DOE]

    This is a request by INDUSTRIAL PARTNERSHIP PROGRAM for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000113

  3. Class Patent Waiver W(C)2009-011

    Broader source: Energy.gov [DOE]

    This is a request by ENHANCED GEOTHERMAL SYSTEMS COMPONENT RESEARCH AND DEVELOPMENT for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-00000075

  4. Advance Patent Waiver W(A)2011-053

    Broader source: Energy.gov [DOE]

    This is a request by VOLVO TECHNOLOGY OF AMERICA, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0004125.

  5. Advance Patent Waiver W(A)2011-023

    Broader source: Energy.gov [DOE]

    This is a request by SCHWEITZER ENGINEERING LAB INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-OE0000537.

  6. Class Patent Waiver W(C)2009-021

    Broader source: Energy.gov [DOE]

    This is a request by ENERGY INNOVATIONS HUBS FUEL FROM SUNLIGHT for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000214

  7. Advance Patent Waiver W(A)2011-071

    Broader source: Energy.gov [DOE]

    This is a request by THE DOW CHEMICAL COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005434.

  8. Advance Patent Waiver W(A)2013-008

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL MOTORS LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005969.

  9. Advance Patent Waiver W(A)2009-063

    Broader source: Energy.gov [DOE]

    This is a request by CREE, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT01577

  10. Advance Patent Waiver W(A)2013-019

    Broader source: Energy.gov [DOE]

    This is a request by CREE, INC. for a DOE waiver of domestic and foreign patent rights under agreement NGB-3-23028-01.

  11. Advance Patent Waiver W(A)2011-025

    Broader source: Energy.gov [DOE]

    This is a request by CREE, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003246.

  12. Advance Patent Waiver W(A)2006-026

    Broader source: Energy.gov [DOE]

    This is a request by CREE, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-06NT42932

  13. Advance Patent Waiver W(A)2009-056

    Broader source: Energy.gov [DOE]

    This is a request by CREE, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000412

  14. Advance Patent Waiver W(A)2005-006

    Broader source: Energy.gov [DOE]

    This is a request by ABENGOA BIOENERGY CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-03GO13142.

  15. Advance Patent Waiver W(A)2009-050

    Broader source: Energy.gov [DOE]

    This is a request by GED INTEGRATED SOLUTIONS for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000167

  16. Advance Patent Waiver W(A)2007-005

    Broader source: Energy.gov [DOE]

    This is a request by EATON CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-06GO16054

  17. Advance Patent Waiver W(A)2009-045

    Broader source: Energy.gov [DOE]

    This is a request by BABCOCK & WILCO for a DOE waiver of domestic and foreign patent rights under agreement DE-AC52-09NA29596

  18. Advance Patent Waiver W(A)2012-005

    Broader source: Energy.gov [DOE]

    This is a request by PHILIPS LUMILEDS LIGHTING, LLC for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0005099.

  19. Advance Patent Waiver W(A)2008-012

    Broader source: Energy.gov [DOE]

    This is a request by DUPONT for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-07GOI7056

  20. Advance Patent Waiver W(A)2011-013

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES RESEARCH CENTER for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003953.

  1. Class Patent Waiver W(C)2012-005

    Broader source: Energy.gov [DOE]

    This is a request by US INDIA JOINT CLEAN ENERGY for a DOE Class patent waiver of domestic and foreign patent rights under agreement DE-FOA-0000506.

  2. Advance Patent Waiver W(A)2011-072

    Broader source: Energy.gov [DOE]

    This is a request by GE GLOBAL RESEARCHH CENTER for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005344.

  3. Advance Patent Waiver W(A)2009-017

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by SPX COOLING TECHNOLOGIES for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-09NT06549

  4. Advance Patent Waiver W(A)2008-013

    Broader source: Energy.gov [DOE]

    This is a request by SANYO ELECTRIC COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-07GO17050

  5. Advance Patent Waiver W(A)2009-006

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES CORP for a DOE waiver of domestic and foreign patent rights under agreement DE-AC02-05CH11231

  6. Advance Patent Waiver W(A)2008-008

    Broader source: Energy.gov [DOE]

    This is a request by PPG INDUSTRIES, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-93CH10554

  7. Advance Patent Waiver W(A)2010-053

    Broader source: Energy.gov [DOE]

    This is a request by PPG INDUSTRIESS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003586

  8. Advance Patent Waiver W(A)2010-032

    Broader source: Energy.gov [DOE]

    This is a request by PPG INDUSTRIES for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003209

  9. Advance Patent Waiver W(A)2004-084

    Broader source: Energy.gov [DOE]

    This is a request by MILLENNIUM INORGANIC CHEMICAL for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-04GO14153.

  10. Advance Patent Waiver W(A)2006-034

    Broader source: Energy.gov [DOE]

    This is a request by ENERGY CONVERSION DEVICES, INC. for a DOE waiver of domestic and foreign patent rights under agreement UNKNOWN

  11. Advance Patent Waiver W(A)2011-029

    Broader source: Energy.gov [DOE]

    This is a request by W. R. GRACE COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000324.

  12. Advance Patent Waiver W(A)2005-005

    Broader source: Energy.gov [DOE]

    This is a request by HONEYWELL, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-00OR22809.

  13. Advance Patent Waiver W(A)2009-036

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL ELECTRIC COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT01579

  14. Advance Patent Waiver W(A)2010-062

    Broader source: Energy.gov [DOE]

    This is a request by PARKER HANNIFIN CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000296

  15. Advance Patent Waiver W(A)2010-022

    Broader source: Energy.gov [DOE]

    This is a request by PHILIPS LUMILEDS for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003210

  16. Advance Patent Waiver W(A)2010-056

    Broader source: Energy.gov [DOE]

    This is a request by PHILIPS RESEARCH LABORATORY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003978

  17. Advance Patent Waiver W(A)2009-001

    Broader source: Energy.gov [DOE]

    This is a request by GE GLOBAL RESEARCHH CENTER for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-GO18085

  18. Class Patent Waiver W(C)2009-014

    Broader source: Energy.gov [DOE]

    This is a request by ENERGY EFFICIENT INFORMATION & COMMUNICATION TECH. for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000107

  19. Class Patent Waiver W(C)2011-001

    Broader source: Energy.gov [DOE]

    This is a request by JEFFERSON SCIENCE ASSOCIATE, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-AC0506OR23177.

  20. Class Patent Waiver W(C)2009-007

    Broader source: Energy.gov [DOE]

    This is a request by HIGH PENETRATION SOLAR DEPLOYMENT for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000085

  1. Class Patent Waiver W(C)2010-006

    Broader source: Energy.gov [DOE]

    This is a request by ARPA ENERGY for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000065

  2. Advance Patent Waiver W(A)2013-016

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL MOTORS LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005753.

  3. Advance Patent Waiver W(A)2013-015

    Broader source: Energy.gov [DOE]

    This is a request by Caterpillar Inc for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005980.

  4. Advance Patent Waiver W(A)2013-005

    Broader source: Energy.gov [DOE]

    This is a request by STATOIL WIND US LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005988.

  5. Advance Patent Waiver W(A)2013-031

    Broader source: Energy.gov [DOE]

    This is a request by WESTINGHOUSE ELECTRIC COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-NE0000566.

  6. Advance Patent Waiver W(A)2013-022

    Broader source: Energy.gov [DOE]

    This is a request by 3M COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005795.

  7. Identified Patent Waiver W(I)2012-015

    Broader source: Energy.gov [DOE]

    This is a request by CERAMATEC, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0000408.

  8. Advance Patent Waiver W(A)2013-018

    Broader source: Energy.gov [DOE]

    This is a request by General Motors, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0006082.

  9. Advance Patent Waiver W(A)2011-048

    Broader source: Energy.gov [DOE]

    This is a request by ADA-ES for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0004343.

  10. Advance Patent Waiver W(A)2008-042

    Broader source: Energy.gov [DOE]

    This is a request by Novozymes Inc. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-0BG01BOBO

  11. Advance Patent Waiver W(A)2011-009

    Broader source: Energy.gov [DOE]

    This is a request by SENER, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003592.

  12. Advance Patent Waiver W(A)2005-014

    Broader source: Energy.gov [DOE]

    This is a request by IBM for a DOE waiver of domestic and foreign patent rights under agreement W-7405-ENG-48.

  13. Class Patent Waiver W(C)2009-004

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by SMART GRID DEMONSTRATIONS for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000036

  14. Advance Patent Waiver W(A)2009-004

    Broader source: Energy.gov [DOE]

    This is a request by SCHLUMBERGER TECHNOLOGY CORP for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18182

  15. Advance Patent Waiver W(A)2011-047

    Broader source: Energy.gov [DOE]

    This is a request by DELPHI AUTOMOTIVE SYSTEMS, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000014.

  16. Advance Patent Waiver W(A)2009-029

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL MOTORS for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-09GO19003

  17. Class Patent Waiver W(C)2012-003

    Broader source: Energy.gov [DOE]

    This is a request by FAST FORWARD PROGRAM for a DOE Class patent waiver of domestic and foreign patent rights under agreement N/A.

  18. Class Patent Waiver W(C)2012-006

    Broader source: Energy.gov [DOE]

    This is a request by LBNL DESIGN FORWARD PROJECT for a DOE Class patent waiver of domestic and foreign patent rights under agreement N/A.

  19. Advance Patent Waiver W(A)2012-034

    Broader source: Energy.gov [DOE]

    This is a request by CORNING INCORPORATED for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0005757.

  20. Advance Patent Waiver W(A)2012-010

    Broader source: Energy.gov [DOE]

    This is a request by 3M COMPANY for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0002980.

  1. Advance Patent Waiver W(A)2011-070

    Broader source: Energy.gov [DOE]

    This is a request by CASCADE ENGINEERING INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005440.

  2. Advance Patent Waiver W(A)2011-028

    Broader source: Energy.gov [DOE]

    This is a request by PPG INDUSTRIES, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0004736.

  3. Advance Patent Waiver W(A)2005-017

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by OSRA for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42341.

  4. Identified Patent Waiver W(I)2011-009

    Broader source: Energy.gov [DOE]

    This is a request by SINTERED POLYCRYSTALLINE for a DOE waiver of domestic and foreign patent rights under agreement DE-AC05-00OR22725.

  5. Identified Patent Waiver W(I)2011-010

    Broader source: Energy.gov [DOE]

    This is a request by THERMALLY CONDUCTIVE for a DOE waiver of domestic and foreign patent rights under agreement DE-AC05-OO0R22725.

  6. Advance Patent Waiver W(A)2008-028

    Broader source: Energy.gov [DOE]

    This is a request by INEOS USA LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-04GO14315

  7. Advance Patent Waiver W(A)2011-001

    Broader source: Energy.gov [DOE]

    This is a request by PRAXAIR, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0004908.

  8. Advance Patent Waiver W(A)2013-007

    Broader source: Energy.gov [DOE]

    This is a request by CA TCHLIGHT ENERGY, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005974.

  9. Advance Patent Waiver W(A)2013-006

    Broader source: Energy.gov [DOE]

    This is a request by PRINCIPLE POWER, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0005987.

  10. Advance Patent Waiver W(A)2013-013

    Broader source: Energy.gov [DOE]

    This is a request by BABCOCK & WILCOX mPOWER for a DOE waiver of domestic and foreign patent rights under agreement DE-NE0000583.

  11. Advance Patent Waiver W(A)2012-031

    Broader source: Energy.gov [DOE]

    This is a request by SRI INTERNATIONAL for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-NT0005578.

  12. Advance Patent Waiver W(A)2012-033

    Broader source: Energy.gov [DOE]

    This is a request by GE-GLOBAL RESEARCH for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-OE000593.

  13. Class Patent Waiver W(C)2008-004

    Broader source: Energy.gov [DOE]

    This is a request by BATTELLE for a DOE waiver of domestic and foreign patent rights under agreement DE-AC07-05ID14517

  14. Class Patent Waiver W(C)2011-012

    Broader source: Energy.gov [DOE]

    This is a request by SOLID STATE LIGHTING PRODUCT DEVELOPMENT ROUND 8 for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000563.

  15. Advance Patent Waiver W(A)2010-040

    Broader source: Energy.gov [DOE]

    This is a request by MODINE MANUFACTURING CO. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0002895

  16. Advance Patent Waiver W(A)2010-019

    Broader source: Energy.gov [DOE]

    This is a request by PRAXAIR, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18063

  17. Class Patent Waiver W(C)2009-005

    Broader source: Energy.gov [DOE]

    This is a request by PHOTOVOLTAIC SUPPLY CHAIN for a DOE waiver of domestic and foreign patent rights under agreement DE-PS36-09GO99003

  18. Identified Patent Waiver W(I)2012-014

    Broader source: Energy.gov [DOE]

    This is a request by CERAMATEC, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0000408.

  19. Advance Patent Waiver W(A)2011-003

    Broader source: Energy.gov [DOE]

    This is a request by PPG INDUSTRIES, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003170.

  20. Advance Patent Waiver W(A)2013-014

    Broader source: Energy.gov [DOE]

    This is a request by W.R GRACE AND CO for a DOE waiver of domestic and foreign patent rights under agreement DE- EE0005991.

  1. Advance Patent Waiver W(A)2011-033

    Broader source: Energy.gov [DOE]

    This is a request by ABB INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-OE0000547.

  2. Advance Patent Waiver W(A)2008-031

    Broader source: Energy.gov [DOE]

    This is a request by Novozymes North America for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43084

  3. Advance Patent Waiver W(A)2005-011

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-05GO15042.

  4. Advance Patent Waiver W(A)2009-020

    Broader source: Energy.gov [DOE]

    This is a request by PRAXAIR, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-NT0005341

  5. Identified Patent Waiver W(I)2011-004

    Broader source: Energy.gov [DOE]

    This is a request by LASER APPARATUS for a DOE waiver of domestic and foreign patent rights under agreement DE-AC04-04AL85000.

  6. Identified Patent Waiver W(I)2008-005

    Broader source: Energy.gov [DOE]

    This is a request by GOURLEY, PAUL for a DOE waiver of domestic and foreign patent rights under agreement DE-AC04-94AL85000

  7. Advance Patent Waiver W(A)2007-002

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by HONEYWELL INTERNATIONAL, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-06NT42947

  8. Identified Patent Waiver W(I)2008-004

    Broader source: Energy.gov [DOE]

    This is a request by RUSSO, A. J. for a DOE waiver of domestic and foreign patent rights under agreement AT(29-1)-789

  9. Advance Patent Waiver W(A)2013-003

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0006108.

  10. Advance Patent Waiver W(A)2006-005

    Broader source: Energy.gov [DOE]

    This is a request by AIR PRODUCTS & CHEMICALS for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-05GO85026

  11. Advance Patent Waiver W(A)2009-062

    Broader source: Energy.gov [DOE]

    This is a request by MICRON TECHNOLOGY INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000141

  12. Advance Patent Waiver W(A)2011-018

    Broader source: Energy.gov [DOE]

    This is a request by ESOLAR for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003595.

  13. Advance Patent Waiver W(A)2011-011

    Broader source: Energy.gov [DOE]

    This is a request by OSRAM SYLVANIA PRODUCTS, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0001361.

  14. Advance Patent Waiver W(A)2010-005

    Broader source: Energy.gov [DOE]

    This is a request by PPG INDUSTRIES for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0001361

  15. Advance Patent Waiver W(A)2012-004

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL ELECTRIC GLOBAL REARCH for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FO0007514.

  16. Identified Patent Waiver W(I)2008-002

    Broader source: Energy.gov [DOE]

    This is a request by NORMANN, RANDY A. for a DOE waiver of domestic and foreign patent rights under agreement DE-AC04-94AL85000

  17. Advance Patent Waiver W(A)2005-055

    Broader source: Energy.gov [DOE]

    This is a request by SIEMEN for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42646.

  18. Advance Patent Waiver W(A)2011-032

    Broader source: Energy.gov [DOE]

    This is a request by SIEMENS ENERGY, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0003714.

  19. Advance Patent Waiver W(A)2012-028

    Broader source: Energy.gov [DOE]

    This is a request by SIEMENS ENERGY, INC. for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-FE0005666.

  20. Advance Patent Waiver W(A)2008-026

    Broader source: Energy.gov [DOE]

    This is a request by Siemens Power Generation for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-98FT40343

  1. Advance Patent Waiver W(A)2005-054

    Broader source: Energy.gov [DOE]

    This is a request by SIEMEN for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42444.

  2. Advance Patent Waiver W(A)2007-022

    Broader source: Energy.gov [DOE]

    This is a request by SIEMENS for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-02NT41247

  3. Advance Patent Waiver W(A)2005-042

    Broader source: Energy.gov [DOE]

    This is a request by MACK TRUCK for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42417.

  4. Advance Patent Waiver W(A)2005-041

    Broader source: Energy.gov [DOE]

    This is a request by MACK TRUCK for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42421.

  5. Advance Patent Waiver W(A)2010-003

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL ELECTRICC GLOBAL RESEARCH for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0000784

  6. Advance Patent Waiver W(A)2010-012

    Broader source: Energy.gov [DOE]

    This is a request by CRAY, INC. for a DOE waiver of domestic and foreign patent rights under agreement B580786

  7. Advance Patent Waiver W(A)2009-067

    Broader source: Energy.gov [DOE]

    This is a request by OSRAM SYLVANIA PRODUCTS, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000611

  8. Identified Patent Waiver W(I)2011-006

    Broader source: Energy.gov [DOE]

    This is a request by SANDIA NATIONAL LABORATORY for a DOE waiver of domestic and foreign patent rights under agreement DE-AC04-95AL85000.

  9. Advance Patent Waiver W(A)2009-055

    Broader source: Energy.gov [DOE]

    This is a request by DUPONT COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0002593

  10. Class Patent Waiver W(C)2009-017

    Broader source: Energy.gov [DOE]

    This is a request by GEOTHERMAL TECHNOLOGIES PROGRAM for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000116

  11. Class Patent Waiver W(C)2012-001

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by ARPA ENERGY for a DOE Class patent waiver of domestic and foreign patent rights under agreement DE-FOA-0000474.

  12. Identified Patent Waiver W(I)2010-004

    Broader source: Energy.gov [DOE]

    This is a request by UOP, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FG26-04NT42121

  13. Identified Patent Waiver W(I)2009-004

    Broader source: Energy.gov [DOE]

    This is a request by URS for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-04NT42314

  14. Advance Patent Waiver W(A)2010-043

    Broader source: Energy.gov [DOE]

    This is a request by JOHNSON CONTROLS, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003841

  15. Advance Patent Waiver W(A)2010-044

    Broader source: Energy.gov [DOE]

    This is a request by JOHNSON CONTROLS, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003982

  16. Advance Patent Waiver W(A)2011-067

    Broader source: Energy.gov [DOE]

    This is a request by GE GLOBAL RESEARCHH CENTER for a DOE waiver of domestic and foreign patent rights under agreement DE-FE0005712.

  17. Advance Patent Waiver W(A)2011-035

    Broader source: Energy.gov [DOE]

    This is a request by 3M COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0004739.

  18. Advance Patent Waiver W(A)2005-037

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by UNITED TCHNOLOGIES for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42453.

  19. Advance Patent Waiver W(A)2005-021

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by UNITED TECHNOLOGIES CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-05GO15151.

  20. Advance Patent Waiver W(A)2009-060

    Broader source: Energy.gov [DOE]

    This is a request by PARKER HANNIFIN CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0000412

  1. Advance Patent Waiver W(A)2008-045

    Broader source: Energy.gov [DOE]

    This is a request by DANISCO US, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18078

  2. Advance Patent Waiver W(A)2010-059

    Broader source: Energy.gov [DOE]

    This is a request by ACUITY BRANDS LIGHTING, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-EE003513

  3. Advance Patent Waiver W(A)2008-025

    Broader source: Energy.gov [DOE]

    This is a request by Grace Davison Company for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-05GO085006

  4. Advance Patent Waiver W(A)2012-011

    Broader source: Energy.gov [DOE]

    This is a request by RAYMOND TINNERMAN MANUFACTURING INC. for a DOE Advance patent waiver of domestic and foreign patent rights under agreement DE-EE0005438.

  5. Advance Patent Waiver W(A)2009-016

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL ELECTRIC COMPANY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18181

  6. Advance Patent Waiver W(A)2009-003

    Broader source: Energy.gov [DOE]

    This is a request by GENERAL MOTOR for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT0804386

  7. Advance Patent Waiver W(A)2008-033

    Broader source: Energy.gov [DOE]

    This is a request by Whitefox Technologies, Limited for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-07NT43090

  8. Advance Patent Waiver W(A)2011-061

    Broader source: Energy.gov [DOE]

    This is a request by ABENGOA SOLAR INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18037.

  9. WA_1994_003_GOLDEN_PHOTOCON_INC_Waiver_of_Domestic_and_Forei.pdf |

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

    Department of Energy WA_1994_003_GOLDEN_PHOTOCON_INC_Waiver_of_Domestic_and_Forei.pdf WA_1994_003_GOLDEN_PHOTOCON_INC_Waiver_of_Domestic_and_Forei.pdf PDF icon WA_1994_003_GOLDEN_PHOTOCON_INC_Waiver_of_Domestic_and_Forei.pdf More Documents & Publications WA_1995_030_GOLDEN_PHOTON_INC_Waiver_of_Domestic_and_Foreign.pdf WA_1993_033_GOLDEN_PHOTON_INC_Waiver_of_Domestic_and_Foreign.pdf WA_03_010_SHELL_SOLAR_INDUSTRIES_Waiver_of_Domestic_and_Fore.pdf

  10. WC_1992_001__Class_WAIVER_OF_the_Governments_US_and_Fore.pdf | Department

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

    of Energy WC_1992_001__Class_WAIVER_OF_the_Governments_US_and_Fore.pdf WC_1992_001__Class_WAIVER_OF_the_Governments_US_and_Fore.pdf PDF icon WC_1992_001__Class_WAIVER_OF_the_Governments_US_and_Fore.pdf More Documents & Publications WC_2000_001_CLASS_WAIVER_BETWEEN_DOE_and_EMPLOYEES_OF_THE_NE.pdf WC_1993_015_CLASS_WAIVER_of_the_Governments_US_and_Foreign_P.pdf Class_Waiver_W_C-2003-001.pdf

  11. WA_01_018_IBM_Waiver_of_Governement_US_and_Foreign_Patent_Ri.pdf |

    Energy Savers [EERE]

    Department of Energy 1_018_IBM_Waiver_of_Governement_US_and_Foreign_Patent_Ri.pdf WA_01_018_IBM_Waiver_of_Governement_US_and_Foreign_Patent_Ri.pdf PDF icon WA_01_018_IBM_Waiver_of_Governement_US_and_Foreign_Patent_Ri.pdf More Documents & Publications WA_04_053_IBM_CORP_Waiver_of_the_Government_U.S._and_Foreign.pdf WA_00_015_COMPAQ_FEDERAL_LLC_Waiver_Domestic_and_Foreign_Pat.pdf Advance Patent Waiver W(A)2002-023

  12. WA_04_047_CATERPILLAR_INC_Waiver_of_Patent_Rights_to_Inventi.pdf |

    Energy Savers [EERE]

    Department of Energy 47_CATERPILLAR_INC_Waiver_of_Patent_Rights_to_Inventi.pdf WA_04_047_CATERPILLAR_INC_Waiver_of_Patent_Rights_to_Inventi.pdf PDF icon WA_04_047_CATERPILLAR_INC_Waiver_of_Patent_Rights_to_Inventi.pdf More Documents & Publications WA_04_046_CATERPILLAR_INC_Waiver_of_Patent_Rights_to_Inventi.pdf WA_04_071_CATERPILLAR_INC_Waiver_of_Patent_Rights_to_Inventi.pdf Advance Patent Waiver W(A)2005-052

  13. WA_97_027_GENERAL_ATOMICS__CORPORATION_Waiver_of_Domestic_an.pdf |

    Energy Savers [EERE]

    Department of Energy 97_027_GENERAL_ATOMICS__CORPORATION_Waiver_of_Domestic_an.pdf WA_97_027_GENERAL_ATOMICS__CORPORATION_Waiver_of_Domestic_an.pdf PDF icon WA_97_027_GENERAL_ATOMICS__CORPORATION_Waiver_of_Domestic_an.pdf More Documents & Publications WA_99_014_UNITED_SOLAR_SYSTEMS_CORP_Waiver_of_Domestic_and_F.pdf Class Patent Waiver W(C)2004-001 WA_97_006_MOTOROLA_MANUFACTURING_SYSTEMS_Waiver_of_Patent_Ri

  14. WC_1993_014_CLASS_WAIVER_of_the_Governments_US_and_Foreign_P.pdf |

    Energy Savers [EERE]

    Department of Energy 14_CLASS_WAIVER_of_the_Governments_US_and_Foreign_P.pdf WC_1993_014_CLASS_WAIVER_of_the_Governments_US_and_Foreign_P.pdf PDF icon WC_1993_014_CLASS_WAIVER_of_the_Governments_US_and_Foreign_P.pdf More Documents & Publications WC_1993_006_CLASS_WAIVER_of_the_Governments_Us_and_Foreign_P.pdf WC_1993_005__CLASS_WAIVER_of_the_Goernment_US_and_Foreign_Pa.pdf WC_1993_003_CLASS_WAIVER__of_the_Government_US_and_Foreign_P

  15. WC_1993_015_CLASS_WAIVER_of_the_Governments_US_and_Foreign_P.pdf |

    Energy Savers [EERE]

    Department of Energy 5_CLASS_WAIVER_of_the_Governments_US_and_Foreign_P.pdf WC_1993_015_CLASS_WAIVER_of_the_Governments_US_and_Foreign_P.pdf PDF icon WC_1993_015_CLASS_WAIVER_of_the_Governments_US_and_Foreign_P.pdf More Documents & Publications Class Patent Waiver W(C)2008-001 WC_1993_003_CLASS_WAIVER__of_the_Government_US_and_Foreign_P.pdf Class Patent Waiver W(C)2008-002

  16. WC_1996_001_CLASS_WAIVER_FOR_LELAND_STANFORD_JUNIOR_UNIVERSI.pdf |

    Energy Savers [EERE]

    Department of Energy 1996_001_CLASS_WAIVER_FOR_LELAND_STANFORD_JUNIOR_UNIVERSI.pdf WC_1996_001_CLASS_WAIVER_FOR_LELAND_STANFORD_JUNIOR_UNIVERSI.pdf PDF icon WC_1996_001_CLASS_WAIVER_FOR_LELAND_STANFORD_JUNIOR_UNIVERSI.pdf More Documents & Publications WC_1993_002_CRADA_CLASS_WAIVER_SOUTHERN_UNIVERSITY_RESEARCH_.pdf WC_1993_008_CLASS_WAIVER_ROCKETDYNE_DIVISION_ROCKWELL_INTERN.pdf WC_1990_012_CLASS_WAIVER_of_Patent_Rights_in_Inventions_Made

  17. WC_2000_001_CLASS_WAIVER_BETWEEN_DOE_and_EMPLOYEES_OF_THE_NE.pdf |

    Energy Savers [EERE]

    Department of Energy 2000_001_CLASS_WAIVER_BETWEEN_DOE_and_EMPLOYEES_OF_THE_NE.pdf WC_2000_001_CLASS_WAIVER_BETWEEN_DOE_and_EMPLOYEES_OF_THE_NE.pdf PDF icon WC_2000_001_CLASS_WAIVER_BETWEEN_DOE_and_EMPLOYEES_OF_THE_NE.pdf More Documents & Publications Class_Waiver_W_C-2000-001.pdf WC_1994_010__CLASS_WAIVER_of_the_Governments_Patent_Rights_.pdf WC_1994_001_CLASS_WAIVER_OF_THE_Governments_Patent_Rights_i

  18. Class Patent Waiver W(C)2008-001

    Broader source: Energy.gov [DOE]

    This is a request by LAWRENCE LIVERMORE NATIONAL SECURITY, LLC (LLNS) for a DOE waiver of domestic and foreign patent rights under agreement DE-AC52-07NA27344

  19. Class Patent Waiver W(C)2008-002

    Broader source: Energy.gov [DOE]

    This is a request by NEVADA NUCLEAR SECURITY SITE for a DOE waiver of domestic and foreign patent rights under agreement DE-AC52-06NA25946

  20. Class Patent Waiver W(C)2008-006

    Broader source: Energy.gov [DOE]

    This is a request by SAVANNAH RIVER NUCLEAR SOLUTIONS for a DOE waiver of domestic and foreign patent rights under agreement DE-AC09-08SR22470

  1. Advance Patent Waiver W(A)2005-031

    Broader source: Energy.gov [DOE]

    This is a request by OSRAM SYLVANIA PRODUCTS, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-05GO85042.

  2. Class Patent Waiver W(C)2009-006

    Broader source: Energy.gov [DOE]

    This is a request by WIND AND HYDROPOWER TECH. for a DOE waiver of domestic and foreign patent rights under agreement DE-PS36-09GO99009

  3. Class Patent Waiver W(C)2012-002

    Broader source: Energy.gov [DOE]

    This is a request by DEMONSTRATION FACILITY PROGRAM (MDF) for a DOE Class patent waiver of domestic and foreign patent rights under agreement DE-AC05-OR22725.

  4. STATEMENT OF CONSIDERATIONS CLASS WAIVER OF THE GOVERNMENT'S...

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

    CONSIDERATIONS CLASS WAIVER OF THE GOVERNMENT'S U.S. AND FOREIGN PATENT RIGHTS IN CERTAIN IDENTIFIED INVENTIONS TO KAISER-HILL ROCKY FLATS MADE IN THE COURSE OF OR UNDER CONTRACT...

  5. Advance Patent Waiver W(A)2009-068

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by United Solar Systems Corp. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-07GO17053

  6. Patent Waivers Approved Before 2003 | Department of Energy

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

    contact the Office of the Assistant General Counsel for Technology Transfer & Intellectual Property at GC-62@hq.doe.gov or (202)-586-2813. File Pre-2003 Patent Waivers Information ...

  7. Identified Patent Waiver W(I)2012-003

    Broader source: Energy.gov [DOE]

    This is a request by UCHICAGO ARGONNE, LLC for a DOE Identified patent waiver of domestic and foreign patent rights under agreement DE-AC02-06CH11357.

  8. Identified Patent Waiver W(I)2012-004

    Broader source: Energy.gov [DOE]

    This is a request by UCHICAGO ARGONNE, LLC for a DOE Identified patent waiver of domestic and foreign patent rights under agreement DE-AC02-06CH11357.

  9. Advance Patent Waiver W(A)2006-021

    Broader source: Energy.gov [DOE]

    This is a request by UTC FUEL CELLS, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-06GO86042

  10. Advance Patent Waiver W(A)2005-053

    Broader source: Energy.gov [DOE]

    This is a request by ALLEGHENY TECHNLOGIES WAH CHANG DIVISION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-05NT42513.

  11. Advance Patent Waiver W(A)2009-047

    Broader source: Energy.gov [DOE]

    This is a request by US SOLAR HOLDINGS LLP for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-08GO18155

  12. Identified Patent Waiver W(I)2010-002

    Broader source: Energy.gov [DOE]

    This is a request by UNIVERSITY OF CALIFORNIA - LBNL for a DOE waiver of domestic and foreign patent rights under agreement DE-AC02-05CH11231

  13. Advance Patent Waiver W(A)2009-002

    Broader source: Energy.gov [DOE]

    This is a request by JOHNSON MATTNEY FUEL CELLS INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-07GO17019

  14. Advance Patent Waiver W(A)2008-007

    Broader source: Energy.gov [DOE]

    This is a request by SCHOTT NORTH AMERICA, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-07GO17001

  15. Advance Patent Waiver W(A)2010-046

    Broader source: Energy.gov [DOE]

    This is a request by NUVERA FUEL CELLS, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-07GO17014

  16. Advance Patent Waiver W(A)2010-051

    Broader source: Energy.gov [DOE]

    This is a request by UT-BATTELLE, LLC for a DOE waiver of domestic and foreign patent rights under agreement DE-AC05-00OR22725

  17. Advance Patent Waiver W(A)2011-068

    Broader source: Energy.gov [DOE]

    This is a request by GE GLOBAL RESEARCHH CENTER for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT05870.

  18. Advance Patent Waiver W(A)2008-004

    Broader source: Energy.gov [DOE]

    This is a request by HUNTSMAN ADVANCED MATERIALS AMERICANS, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FG36-07GO17012

  19. Advance Patent Waiver W(A)2008-029

    Broader source: Energy.gov [DOE]

    This is a request by BALLARD POWER SYSTEM, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-07GO17017

  20. Advance Patent Waiver W(A)2008-040

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by W. L. GORE & ASSOCIATES, INC, for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-08GO18052

  1. Class Patent Waiver W(C)2011-011

    Broader source: Energy.gov [DOE]

    This is a request by SOLID STATE LIGHTING U.S. MANUFACTURING- ROUND 3 for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000561.

  2. Advance Patent Waiver W(A)2008-030

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by DOW CORNING CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-OBG01B02B

  3. CDPHE Construction Storm Water Forms R-Factor Waiver Application...

    Open Energy Info (EERE)

    CDPHE Construction Storm Water Forms R-Factor Waiver Application Jump to: navigation, search OpenEI Reference LibraryAdd to library Legal Document- Permit ApplicationPermit...

  4. Class Patent Waiver W(C)2004-001

    Broader source: Energy.gov [DOE]

    This is a request by WESTINGHOUSE SAVANNAH RIVER COMPANY (WSRC) for a DOE waiver of domestic and foreign patent rights under agreement DE-AC09-96SR18500.

  5. Class Patent Waiver W(C)2011-010

    Broader source: Energy.gov [DOE]

    This is a request by CONSORTIUM FOR ADVANCED SIMULATION OF LIGHT WATER REACTORS for a DOE waiver of domestic and foreign patent rights under agreement DE-FOA-0000170.

  6. Class Patent Waiver W(C)2012-004

    Broader source: Energy.gov [DOE]

    This is a request by BIOENERGY SCIENCE CENTER (BESC) for a DOE Class patent waiver of domestic and foreign patent rights under agreement DE-AC05-00OR22725.

  7. Class Patent Waiver W(C)2012-007

    Broader source: Energy.gov [DOE]

    This is a request by SOLID-STATE LIGHTING ROUND 4 for a DOE Class patent waiver of domestic and foreign patent rights under agreement DE-FOA-0000792.

  8. Identified Patent Waiver W(I)2012-012

    Broader source: Energy.gov [DOE]

    This is a request by DR. F. JEFFREY MARTIN for a DOE Identified patent waiver of domestic and foreign patent rights under agreement DE-AC52-06NA25396.

  9. Identified Patent Waiver W(I)2012-005

    Broader source: Energy.gov [DOE]

    This is a request by UCHICAGO ARGONNE, LLC for a DOE Identified patent waiver of domestic and foreign patent rights under agreement DE-AC02-06CH11357.

  10. Advance Patent Waiver W(A)2005-010

    Broader source: Energy.gov [DOE]

    This is a request by ABB LUMMUS GLOBAL, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-04GO14151.

  11. Advance Patent Waiver W(A)2010-042

    Broader source: Energy.gov [DOE]

    This is a request by UNIVERSITY OF NORTH DAKOTA for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT43291

  12. Advance Patent Waiver W(A)2010-033

    Office of Energy Efficiency and Renewable Energy (EERE)

    This is a request by ROLLS ROYCE FUEL SYSTEMS for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-08NT01911

  13. Identified Patent Waiver W(I)2012-009

    Broader source: Energy.gov [DOE]

    This is a request by UNITED TECHNOLOGIES RESEARCH for a DOE Identified patent waiver of domestic and foreign patent rights under agreement DE-AC02-05CH11231.

  14. Advance Patent Waiver W(A)2005-007

    Broader source: Energy.gov [DOE]

    This is a request by AIR PRODUCTS AND CHEMICALS, INC for a DOE waiver of domestic and foreign patent rights under agreement DE-FC36-04GO13030.

  15. Class Patent Waiver W(C)2008-007

    Broader source: Energy.gov [DOE]

    This is a request by NEW YORK BLUE SUPERCOMPUTER for a DOE waiver of domestic and foreign patent rights under agreement DE-AC02-98CH10886

  16. Identified Patent Waiver W(I)2012-002

    Broader source: Energy.gov [DOE]

    This is a request by BATTELLE MEMORIAL INSTITUTE for a DOE Identified patent waiver of domestic and foreign patent rights under agreement DE-AC07-05ID14517.

  17. File:04NVCMonitoringWellWaiver (1).pdf | Open Energy Information

    Open Energy Info (EERE)

    4NVCMonitoringWellWaiver (1).pdf Jump to: navigation, search File File history File usage Metadata File:04NVCMonitoringWellWaiver (1).pdf Size of this preview: 463 599 pixels....

  18. WA_04_069__EATON_CORPORATION_Waiver_of_Domestic_and_Foreign_.pdf |

    Energy Savers [EERE]

    Department of Energy 69__EATON_CORPORATION_Waiver_of_Domestic_and_Foreign_.pdf WA_04_069__EATON_CORPORATION_Waiver_of_Domestic_and_Foreign_.pdf PDF icon WA_04_069__EATON_CORPORATION_Waiver_of_Domestic_and_Foreign_.pdf More Documents & Publications WA_04_059_EATON_CORPORATION_Waiver_of_Patent_Rights_Under_a_.pdf WA_02_048_EATON_CORPORATION_Waviver_of_Patent_Rights_Under_A.pdf WA_04_074_EATON_CORPORATION_Waiver_of_Domestic_and_Foreign_I.pdf

  19. Comparison of SPME headspace analysis to U.S. EPA method5030/8260B for MTBE monitoring

    SciTech Connect (OSTI)

    Stringfellow, William T.; Oh, Kuen-Chan

    2005-02-01

    A novel method for analysis of methyl tert-butyl ether andtert-butyl alcohol using solid phase microextraction is described andcompared to a standard method.

  20. Advance Patent Waiver W(A)2008-006 | Department of Energy

    Energy Savers [EERE]

    8-006 Advance Patent Waiver W(A)2008-006 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by CATERPILLAR, INC under agreement DE-FC26-00AL67017, as the DOE has determined that granting such a waiver best serves the interests of the United States and the general public. PDF icon Advance Patent Waiver W(A)2008-006 More Documents & Publications

  1. Advance Patent Waiver W(A)2010-037 | Department of Energy

    Energy Savers [EERE]

    7 Advance Patent Waiver W(A)2010-037 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by ALCATEL-LUCENT USA INC. under agreement DE-EE0002895, as the DOE has determined that granting such a waiver best serves the interests of the United States and the general public. PDF icon Advance Patent Waiver W(A)2010-037 More Documents & Publications A

  2. Advance Patent Waiver W(A)2010-038 | Department of Energy

    Energy Savers [EERE]

    8 Advance Patent Waiver W(A)2010-038 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by ALCATEL-LUCENT USA INC. under agreement DE-EE0002887, as the DOE has determined that granting such a waiver best serves the interests of the United States and the general public. PDF icon Advance Patent Waiver W(A)2010-038 More Documents & Publications A

  3. POLICY GUIDANCE MEMORANDUM #11A Approval Process for Dual Compensation Waivers for Reemployed Annuitants

    Broader source: Energy.gov [DOE]

    Process to  grant dual compensation (salary-offset) waivers to reemployed annuitants who work on a limited basis without reduction to their retirement annuity.

  4. Advance Patent Waiver W(A)2006-028 | Department of Energy

    Energy Savers [EERE]

    6-028 Advance Patent Waiver W(A)2006-028 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by COLONY PROJECT under agreement SUBC-B555909, as the DOE has determined that granting such a waiver best serves the interests of the United States and the general public. PDF icon Advance Patent Waiver W(A)2006-028 More Documents & Publications Advance Patent Waiver W(A)2005-048 2011_INCITE_Fact_Sheets.pdf

  5. Advance Patent Waiver W(A)2012-021 | Department of Energy

    Energy Savers [EERE]

    2-021 Advance Patent Waiver W(A)2012-021 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by USEC, INC. under agreement DE-NE0000488, as the DOE has determined that granting such a waiver best serves the interests of the United States and the general public. PDF icon Advance Patent Waiver W(A)2012-021 More Documents & Publications WA_1993_042_UNITED_TECHNOLOGIES_CORPORATION_Waiver_of_the_Go.pdf

  6. WC_1995_010__PETITION_FOR_CLASS_WAIVER_for_KAISER_HILL_CO_In...

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

    ETITIONFORCLASSWAIVERforKAISERHILLCOIn.pdf More Documents & Publications WC1995011CLASSWAIVERforKAISERHILLCOManagementContr.pdf ClassWaiverWC-2002-003.pdf...

  7. STATEMENT OF CONSIDERATIONS CLASS WAIVER OF U.S. AND FOREIGN...

    Office of Environmental Management (EM)

    subject to this Class Waiver also agree that any products embodying any waived invention or produced through the use of any w aived invention will be manufactured...

  8. Guidance on Waivers of Premium Pay To Meet A Critical Need

    Broader source: Energy.gov [DOE]

    This document contains guidance on the waiver of the biweekly limit on premium pay for overtime work that is critical to an agency's mission

  9. Identified Patent Waiver W(I)2010-009 | Department of Energy

    Energy Savers [EERE]

    9 Identified Patent Waiver W(I)2010-009 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by SCHWEITZER ENGINEERING LAB INC. under agreement DE-FC26-07NT43311, as the DOE has determined that granting such a waiver best serves the interests of the United States and the general public. PDF icon Identified Patent Waiver W(I)2010-009 More Documents & Publications Hallmark Cryptographic Serial Communication

  10. Statement from Secretary Bodman on Signing of the Jones Act Waiver |

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

    Department of Energy from Secretary Bodman on Signing of the Jones Act Waiver Statement from Secretary Bodman on Signing of the Jones Act Waiver September 26, 2005 - 10:52am Addthis WASHINGTON, DC - Please find below a statement from Department of Energy Secretary Samuel W. Bodman on DHS Secretary Chertoff's decision to waive the Jones Act. This waiver will allow foreign as well as U.S. shipping vessels to transport petroleum and refined petroleum products (gasoline and diesel) until 12:01

  11. Class Patent Waiver W(C)2009-001 | Department of Energy

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

    Class Patent Waiver W(C)2009-001 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by ...

  12. Identified Patent Waiver W(I)2010-005 | Department of Energy

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

    Identified Patent Waiver W(I)2010-005 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by ...

  13. Advance Patent Waiver W(A)2010-006 | Department of Energy

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

    Advance Patent Waiver W(A)2010-006 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by ...

  14. Identified Patent Waiver W(I)2010-006 | Department of Energy

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

    Identified Patent Waiver W(I)2010-006 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice by ...

  15. DOE Solicits Views on the Implementation of Large-Capacity Clothes Washer Waivers

    Broader source: Energy.gov [DOE]

    The Department of Energy has recently granted several requests for waivers establishing an alternative test procedure for certain large-capacity residential clothes washer models.  We have now...

  16. DOE Receives Responses on the Implementation of Large-Capacity Clothes Washer Waivers

    Broader source: Energy.gov [DOE]

    The Department last week invited interested parties to submit views on the proper application of waivers establishing alternative test procedures for existing large-capacity residential clothes...

  17. Alaska ADEC Process for Issuing a 401 Waiver of Corps 404 Permits...

    Open Energy Info (EERE)

    Environmental Conservation. ADEC Process for Issuing a 401 Waiver of Corps 404 Permits. 4p. GuideHandbook sent to Retrieved from "http:en.openei.orgwindex.php?titleAlaskaAD...

  18. WPN 94-8: 40 Percent Waiver Provisions for Mobile Home Units

    Broader source: Energy.gov [DOE]

    This program notice provides clarifying guidance previously issued under Weatherization Program Notice 93-14 on mobile home units weatherized by states which adopt the approved 4.0 version of NEAT or other similar approved energy audits and receive a waiver of the 40 percent requirement from DOE.

  19. WPN 93-14: 40 Percent Waiver Provisions for Multifamily and Mobile Home Units

    Broader source: Energy.gov [DOE]

    This program notice provides guidance on multifamily and mobile home units weatherized by states, which adopt the approved 4.0 version of NEAT or other similar approved energy audits and receive a waiver of the 40 percent requirement from DOE.

  20. Alternative Compliance: Guidelines for Preparing and Submitting a Waiver Request Application and Other Documentation Requirements (Book)

    SciTech Connect (OSTI)

    Not Available

    2010-11-01

    This document is designed to assist covered fleets interested in taking advantage of more flexible compliance options and to facilitate the transition from Standard Compliance to Alternative Compliance. It is designed to help fleets better understand the Alternative Compliance option and successfully complete the waiver application process.

  1. Alternative Compliance: Guidelines for Preparing and Submitting a Waiver Request Application and Other Documentation Requirements

    SciTech Connect (OSTI)

    Not Available

    2013-03-01

    This document is designed to assist covered fleets interested in taking advantage of more flexible compliance options and to facilitate the transition from Standard Compliance to Alternative Compliance. It is designed to help fleets better understand the Alternative Compliance option and successfully complete the waiver application process.

  2. Alternative Compliance: Guidelines for Preparing and Submitting a Waiver Request Application and Other Documentation Requirements (Book)

    SciTech Connect (OSTI)

    Sears, T.

    2014-01-01

    This document is designed to assist covered fleets interested in taking advantage of more flexible compliance options and to facilitate the transition from Standard Compliance to Alternative Compliance. It is designed to help fleets better understand the Alternative Compliance option and successfully complete the waiver application process.

  3. Alternative Compliance: Guidelines for Preparing and Submitting a Waiver Request Application and Other Documentation Requirements (Brochure)

    SciTech Connect (OSTI)

    Not Available

    2014-06-01

    This document is designed to assist covered fleets interested in taking advantage of more flexible compliance options and to facilitate the transition from Standard Compliance to Alternative Compliance. It is designed to help fleets better understand the Alternative Compliance option and successfully complete the waiver application process.

  4. Combustion characterization of methylal in reciprocating engines

    SciTech Connect (OSTI)

    Dodge, L.; Naegeli, D.

    1994-06-01

    Methylal, CH{sub 3}OCH{sub 2}OCH{sub 3}, also known as dimethoxy-methane, is unique among oxygenates in that it has a low autoignition temperature, no carbon-carbon bonds, and is soluble in middle distillate fuels. Because of these properties, methylal has been shown to be a favorable fuel additive for reducing smoke in diesel engines. Recent measurements of ignition delay times indicate that methylal has a cetane number in the range of 45-50, which is compatible with diesel fuels. Engine tests have shown that adding methylal to diesel fuel significantly reduces smoke emissions. Gaseous emissions and combustion efficiencies obtained with methylal/diesel fuel blends remain essentially the same as those measured using neat diesel fuel. Lubricity measurements of methylal/diesel fuel blends with a ball on cylinder lubrication evaluator (BOCLE) show that methylal improves the lubricity of diesel fuel. Even though additions of methylal lower the fuel viscosity, the results of the BOCLE tests indicate that the methylal/diesel fuel blends cause less pump wear than neat diesel fuel. The one drawback is that methylal has a low boiling point (42{degrees}C) and a relatively high vapor pressure. As a result, it lowers the flash point of diesel fuel and causes a potential fuel tank flammability hazard. One solution to this increased volatility is to make polyoxymethylenes with the general formula of CH{sub 3}O(CH{sub 2}O){sub x}CH{sub 3} where x > 2. The molecules are similar to methylal, but have higher molecular weights and thus higher viscosities and substantially lower vapor pressures. Therefore, their flash points will be compatible with regular diesel fuel. The polyoxymethylenes are expected to have combustion properties similar to methylal. It is theorized that by analogy with hydrocarbons, the ignition quality (i.e., cetane number) of the polyoxymethylenes will be better than that of methylal.

  5. EXTRACTION OF TETRAVALENT PLUTONIUM VALUES WITH METHYL ETHYL KETONE, METHYL ISOBUTYL KETONE ACETOPHENONE OR MENTHONE

    DOE Patents [OSTI]

    Seaborg, G.T.

    1961-08-01

    A process is described for extracting tetravalent plutonium from an aqueous acid solution with methyl ethyl ketone, methyl isobutyl ketone, or acetophenone and with the extraction of either tetravalent or hexavalent plutonium into menthone. (AEC)

  6. MTEM Map

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

    MTBE Production Economics Tancred C. M. Lidderdale Contents 1. Summary 2. MTBE Production Costs 3. Relationship between price of MTBE and Reformulated Gasoline 4. Influence of Natural Gas Prices on the Gasoline Market 5. Regression Results 6. Data Sources 7. End Notes 1. Summary Last year the price of MTBE (methyl tertiary butyl ether) increased dramatically on two occasions (Figure 1) (see Data Sources at end of article.): 1. Between April and June 2000, the price (U.S. Gulf Coast waterborne

  7. untitled

    Gasoline and Diesel Fuel Update (EIA)

    of "other" hydrocarbons and oxygenates include hydrogen and oxygenates especially fuel ethanol and methyl tertiary butyl ether (MTBE). The adjustment is equal to the...

  8. This Week In Petroleum Printer-Friendly Version

    Annual Energy Outlook [U.S. Energy Information Administration (EIA)]

    this transition from Methyl Tertiary Butyl Ether (MTBE) reformulated gasoline (RFG) to ethanol RFG, since ethanol is not blended into the gasoline mixture until just before the...

  9. Motor Gasoline Market Spring 2007 and Implications for Spring...

    Annual Energy Outlook [U.S. Energy Information Administration (EIA)]

    began to decline, and with the transition from methyl tertiary butyl ether (MTBE) to ethanol completed and the end of the summer driving season drawing near, gasoline prices...

  10. Methylal and Methylal-Diesel Blended Fuels from Use In Compression-Ignition Engines

    SciTech Connect (OSTI)

    Keith D. Vertin; James M. Ohi; David W. Naegeli; Kenneth H. Childress; Gary P. Hagen; Chris I. McCarthy; Adelbert S. Cheng; Robert W. Dibble

    1999-05-05

    Gas-to-liquids catalytic conversion technologies show promise for liberating stranded natural gas reserves and for achieving energy diversity worldwide. Some gas-to-liquids products are used as transportation fuels and as blendstocks for upgrading crude derived fuels. Methylal (CH{sub 3}-O-CH{sub 2}-O-CH{sub 3}) also known as dimethoxymethane or DMM, is a gas-to-liquid chemical that has been evaluated for use as a diesel fuel component. Methylal contains 42% oxygen by weight and is soluble in diesel fuel. The physical and chemical properties of neat methylal and for blends of methylal in conventional diesel fuel are presented. Methylal was found to be more volatile than diesel fuel, and special precautions for distribution and fuel tank storage are discussed. Steady state engine tests were also performed using an unmodified Cummins 85.9 turbocharged diesel engine to examine the effect of methylal blend concentration on performance and emissions. Substantial reductions of particulate matter emissions h ave been demonstrated 3r IO to 30% blends of methylal in diesel fuel. This research indicates that methylal may be an effective blendstock for diesel fuel provided design changes are made to vehicle fuel handling systems.

  11. Low temperature synthesis of methyl formate

    DOE Patents [OSTI]

    Mahajan, Devinder; Slegeir, William A.; Sapienza, Richard S.; O'Hare, Thomas E.

    1986-01-01

    A gas reaction process for the preferential production of methyl formate over the co-production of methanol wherein the reactant ratio of CO/H.sub.2 is upgraded and this reaction takes place at low temperatures of 50.degree.-150.degree. C. and moderate pressures of .gtoreq.100 psi.

  12. Modulation of histone methylation and MLH1 gene silencing by...

    Office of Scientific and Technical Information (OSTI)

    ... Subject: 60 APPLIED LIFE SCIENCES; ARGININE; CARCINOGENS; CHROMIUM; DNA DAMAGES; GENES; HUMAN POPULATIONS; LUNGS; LYSINE; METHYLATION; NEOPLASMS; OCCUPATIONAL EXPOSURE; PROMOTERS ...

  13. Conference Waiver

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

    Issues Special Interest Group May 6-10, 2013 -Chicago, ... focus on such critical issues as the safety of nuclear facilities as it relates to beyond design basis events analysis ...

  14. Major sources to waivers - lessons learned and $ saved at two U.S. Navy facilities

    SciTech Connect (OSTI)

    Klitsch, M.

    1997-12-31

    Naval Surface Warfare Center Carderock Division (NSWCCD) manages 17 US Navy research and development (R and D) facilities across the country. These include two facilities in Maryland -- one in Annapolis and the other in West Bethesda which is better known as Carderock. NO{sub x} is the only air emission which exceeds a threshold limit at both properties. The potential to emit NO{sub x} is 72 tpy for Annapolis and 51 tpy for Carderock. The facilities are in different counties but each county has a trigger limit for NO{sub x} of 25 tpy making both facilities major sources. In preparation for the Title V permit applications to the state of Maryland, Carderock budgeted $150,000 in fiscal year 1996 to have a contractor conduct air emission inventories and prepare the Title V permits for both Carderock and Annapolis. However, the Carderock Air Program Manager did not pursue a contractor to perform the work but personally conducted the air emission inventory for both Annapolis and Carderock. Noticing a large difference between the potential-to-emit and the actual emissions of NO{sub x}, the Air Program Manager began negotiations with the Maryland Department of the Environment (MDE) to waive the requirement for the Title V permit application. MDE responded in December 1996 that if the facility`s actual emissions would not exceed 50% of any of the threshold limits during any 12 month period, then a letter of understanding stating such should be submitted to MDE. This letter of understanding would be recognized by the US EPA and MDE and would act as a waiver to the Title V permit applicability up to July 31, 1998. Carderock and Annapolis meet this requirement and letters of understanding were drafted and sent to MDE in January 1997.

  15. An Experimental and Kinetic Modeling Study of Methyl Decanoate Combustion

    SciTech Connect (OSTI)

    Sarathy, S M; Thomson, M J; Pitz, W J; Lu, T

    2010-02-19

    Biodiesel is typically a mixture of long chain fatty acid methyl esters for use in compression ignition engines. Improving biofuel engine performance requires understanding its fundamental combustion properties and the pathways of combustion. This research study presents new combustion data for methyl decanoate in an opposed-flow diffusion flame. An improved detailed chemical kinetic model for methyl decanoate combustion is developed, which serves as the basis for deriving a skeletal mechanism via the direct relation graph method. The novel skeletal mechanism consists of 648 species and 2998 reactions. This mechanism well predicts the methyl decanoate opposed-flow diffusion flame data. The results from the flame simulations indicate that methyl decanoate is consumed via abstraction of hydrogen atoms to produce fuel radicals, which lead to the production of alkenes. The ester moiety in methyl decanoate leads to the formation of low molecular weight oxygenated compounds such as carbon monoxide, formaldehyde, and ketene.

  16. Conversion of Levulinic Acid to Methyl Tetrahydrofuran - Energy...

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

    acid is a highly desirable renewable chemical platform, which, using this process, can be converted into Methyl Tetrahydrofuran (Me-THF) with reasonable yield. The...

  17. Lithium Methyl Carbonate as a Reaction Product of Metallic Lithiumand...

    Office of Scientific and Technical Information (OSTI)

    Lithium methyl carbonate is only one of the components, the others being lithium oxalate and lithium methoxide. Authors: Zhuang, Guorong V. ; Yang, Hui ; Ross Jr., Philip N. ; Xu, ...

  18. Theoretical spectroscopic characterization at low temperatures of S-methyl thioformate and O-methyl thioformate

    SciTech Connect (OSTI)

    Senent, M. L.; Puzzarini, C.; Hochlaf, M.; Domínguez-Gómez, R.; Carvajal, M.

    2014-09-14

    Highly correlated ab initio methods are employed to determine spectroscopic properties at low temperatures of two S-analogs of methyl formate: S-methyl thioformate CH{sub 3}-S-CHO (MSCHO) and O-methyl thioformate CH{sub 3}-O-CHS (MOCHS). Both species are detectable and they are expected to play an important role in Astrochemistry. Molecular properties are compared with those of the O-analog, methyl formate. Both isomers present two conformers cis and trans. cis-CH{sub 3}-S-CHO represents the most stable structure lying 4372.2 cm{sup −1} below cis-CH{sub 3}-O-CHS. The energy difference between the cis and trans forms is drastically lower for MSCHO (1134 cm{sup −1}) than for MOCHS (1963.6 cm{sup −1}). Harmonic and anharmonic fundamentals and the corresponding intensities, as well as the rotational constants for the ground vibrational and first excited torsional states and the centrifugal distortions constants, are provided. Low torsional energy levels have been obtained by solving variationally a two dimensional Hamiltonian expressed in terms of the two torsional degrees of freedom. The corresponding 2D potential energy surfaces have been computed at the CCSD(T)/aug-cc-pVTZ level of theory. The methyl torsional barriers V{sub 3}(cis) are determined to be 139.7 cm{sup −1} (CH{sub 3}-S-CHO) and 670.4 cm{sup −1} (CH{sub 3}-O-CHS). The A/E splitting of ground torsional state has been estimated to be 0.438 cm{sup −1} for CH{sub 3}-S-CHO and negligible for CH{sub 3}-O-CHS.

  19. Methyl tert-butyl ether and ethyl tert-butyl ether: A comparison of properties, synthesis techniques, and operating conditions

    SciTech Connect (OSTI)

    Sneesby, M.G.; Tade, M.O.; Datta, R.

    1996-12-31

    MTBE is currently the most industrially significant oxygenate but some of the properties of ETBE and the EPA ethanol mandate suggest that ETBE could become a viable competitor. Similar synthesis techniques are used for both ethers but the phase behaviour of the ETBE system requires slightly different operating conditions and creates some alternatives for product recovery. The process control strategy for both systems must address some unusual challenges. 9 refs., 1 tab.

  20. Production of methyl-vinyl ketone from levulinic acid

    DOE Patents [OSTI]

    Dumesic, James A.; West; Ryan M.

    2011-06-14

    A method for converting levulinic acid to methyl vinyl ketone is described. The method includes the steps of reacting an aqueous solution of levulinic acid, over an acid catalyst, at a temperature of from room temperature to about 1100 K. Methyl vinyl ketone is thereby formed.

  1. Host cells and methods for producing 3-methyl-2-buten-1-ol, 3-methyl-3-buten-1-ol, and 3-methyl-butan-1-ol

    DOE Patents [OSTI]

    Chou, Howard H.; Keasling, Jay D.

    2011-07-26

    The invention provides for a method for producing a 5-carbon alcohol in a genetically modified host cell. In one embodiment, the method comprises culturing a genetically modified host cell which expresses a first enzyme capable of catalyzing the dephosphorylation of an isopentenyl pyrophosphate (IPP) or dimethylallyl diphosphate (DMAPP), such as a Bacillus subtilis phosphatase (YhfR), under a suitable condition so that 5-carbon alcohol is 3-methyl-2-buten-1-ol and/or 3-methyl-3-buten-1-ol is produced. Optionally, the host cell may further comprise a second enzyme capable of reducing a 3-methyl-2-buten-1-ol to 3-methyl-butan-1-ol, such as a reductase.

  2. Role of methyl groups in dynamics and evolution of biomolecules

    SciTech Connect (OSTI)

    Nickels, Jonathan D [ORNL; Curtis, J. E. [National Institute of Standards and Technology (NIST), Gaithersburg, MD; Oneill, Hugh [Oak Ridge National Laboratory (ORNL); Sokolov, Alexei P [ORNL

    2012-01-01

    Recent studies have discovered strong differences between the dynamics of nucleic acids (RNA and DNA) and proteins, especially at low hydration and low temperatures. This difference is caused primarily by dynamics of methyl groups that are abundant in proteins, but are absent or very rare in RNA and DNA. In this paper, we present a hypothesis regarding the role of methyl groups as intrinsic plasticizers in proteins and their evolutionary selection to facilitate protein dynamics and activity. We demonstrate the profound effect methyl groups have on protein dynamics relative to nucleic acid dynamics, and note the apparent correlation of methyl group content in protein classes and their need for molecular flexibility. Moreover, we note the fastest methyl groups of some enzymes appear around dynamical centers such as hinges or active sites. Methyl groups are also of tremendous importance from a ydrophobicity/folding/entropy perspective. These significant roles, however, complement our hypothesis rather than preclude the recognition of methyl groups in the dynamics and evolution of biomolecules.

  3. Dcm methylation is detrimental to plasmid transformation in Clostridium thermocellum

    SciTech Connect (OSTI)

    Guss, Adam M; Olson, Daniel G.; Caiazza, Nicky; Lynd, Lee R

    2012-01-01

    BACKGROUND: Industrial production of biofuels and other products by cellulolytic microorganisms is of interest but hindered by the nascent state of genetic tools. Although a genetic system for Clostridium thermocellum DSM1313 has recently been developed, available methods achieve relatively low efficiency and similar plasmids can transform C. thermocellum at dramatically different efficiencies. RESULTS: We report an increase in transformation efficiency of C. thermocellum for a variety of plasmids by using DNA that has been methylated by Escherichia coli Dam but not Dcm methylases. When isolated from a dam+ dcm+ E. coli strain, pAMG206 transforms C. thermocellum 100-fold better than the similar plasmid pAMG205, which contains an additional Dcm methylation site in the pyrF gene. Upon removal of Dcm methylation, transformation with pAMG206 showed a four- to seven-fold increase in efficiency; however, transformation efficiency of pAMG205 increased 500-fold. Removal of the Dcm methylation site from the pAM205 pyrF gene via silent mutation resulted in increased transformation efficiencies equivalent to that of pAMG206. Upon proper methylation, transformation efficiency of plasmids bearing the pMK3 and pB6A origins of replication increased ca. three orders of magnitude. CONCLUSION: E. coli Dcm methylation decreases transformation efficiency in C. thermocellum DSM1313. The use of properly methylated plasmid DNA should facilitate genetic manipulation of this industrially relevant bacterium.

  4. Phase 2 Methyl Iodide Deep-Bed Adsorption Tests

    SciTech Connect (OSTI)

    Soelberg, Nick; Watson, Tony

    2014-09-01

    Nuclear fission produces fission products (FPs) and activation products, including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Research, demonstrations, and some reprocessing plant experience have indicated that diatomic iodine can be captured with efficiencies high enough to meet regulatory requirements. Research on the capture of organic iodides has also been performed, but to a lesser extent. Several questions remain open regarding the capture of iodine bound in organic compounds. Deep-bed methyl iodide adsorption testing has progressed according to a multi-laboratory methyl iodide adsorption test plan. This report summarizes the second phase of methyl iodide adsorption work performed according to this test plan using the deep-bed iodine adsorption test system at the Idaho National Laboratory (INL), performed during the second half of Fiscal Year (FY) 2014. Test results continue to show that methyl iodide adsorption using AgZ can achieve total iodine decontamination factors (DFs, ratios of uncontrolled and controlled total iodine levels) above 1,000, until breakthrough occurred. However, mass transfer zone depths are deeper for methyl iodide adsorption compared to diatomic iodine (I2) adsorption. Methyl iodide DFs for the Ag Aerogel test adsorption efficiencies were less than 1,000, and the methyl iodide mass transfer zone depth exceeded 8 inches. Additional deep-bed testing and analyses are recommended to (a) expand the data base for methyl iodide adsorption under various conditions specified in the methyl iodide test plan, and (b) provide more data for evaluating organic iodide reactions and reaction byproducts for different potential adsorption conditions.

  5. Substantial improvements in methyl ketone production in E. coli and

    Office of Scientific and Technical Information (OSTI)

    insights on the pathway from in vitro studies (Journal Article) | SciTech Connect Journal Article: Substantial improvements in methyl ketone production in E. coli and insights on the pathway from in vitro studies Citation Details In-Document Search Title: Substantial improvements in methyl ketone production in E. coli and insights on the pathway from in vitro studies Authors: Goh, Ee-Been ; Baidoo, Edward E.K. ; Burd, Helcio ; Lee, Taek Soon ; Keasling, Jay D. ; Beller, Harry R. Publication

  6. Distributions of methyl group rotational barriers in polycrystalline organic solids

    SciTech Connect (OSTI)

    Beckmann, Peter A. E-mail: wangxianlong@uestc.edu.cn; Conn, Kathleen G.; Division of Education and Human Services, Neumann University, One Neumann Drive, Aston, Pennsylvania 19014-1298 ; Mallory, Clelia W.; Department of Chemistry, Bryn Mawr College, 101 North Merion Ave., Bryn Mawr, Pennsylvania 19010-2899 ; Mallory, Frank B.; Rheingold, Arnold L.; Rotkina, Lolita; Wang, Xianlong E-mail: wangxianlong@uestc.edu.cn

    2013-11-28

    We bring together solid state {sup 1}H spin-lattice relaxation rate measurements, scanning electron microscopy, single crystal X-ray diffraction, and electronic structure calculations for two methyl substituted organic compounds to investigate methyl group (CH{sub 3}) rotational dynamics in the solid state. Methyl group rotational barrier heights are computed using electronic structure calculations, both in isolated molecules and in molecular clusters mimicking a perfect single crystal environment. The calculations are performed on suitable clusters built from the X-ray diffraction studies. These calculations allow for an estimate of the intramolecular and the intermolecular contributions to the barrier heights. The {sup 1}H relaxation measurements, on the other hand, are performed with polycrystalline samples which have been investigated with scanning electron microscopy. The {sup 1}H relaxation measurements are best fitted with a distribution of activation energies for methyl group rotation and we propose, based on the scanning electron microscopy images, that this distribution arises from molecules near crystallite surfaces or near other crystal imperfections (vacancies, dislocations, etc.). An activation energy characterizing this distribution is compared with a barrier height determined from the electronic structure calculations and a consistent model for methyl group rotation is developed. The compounds are 1,6-dimethylphenanthrene and 1,8-dimethylphenanthrene and the methyl group barriers being discussed and compared are in the 212 kJ?mol{sup ?1} range.

  7. Rape oil methyl ester (RME) and used cooking oil methyl ester (UOME) as alternative fuels

    SciTech Connect (OSTI)

    Hohl, G.H.

    1995-12-31

    The author presents a review about the fleet tests carried out by the Austrian Armed Forces concerning the practical application of a vegetable oil, i.e Rape Oil Methyl Ester (RME) and Used Cooking Oil Methyl Ester (UOME) as alternative fuels for vehicles under military conditions, and reviews other research results carried out in Austria. As a result of over-production in Western European agriculture, the increase in crop yields has led to tremendous surpluses. Alternative agricultural products have been sought. One alternative can be seen in biological fuel production for tractors, whereby the farmer is able to produce his own fuel supply as was the case when he previously provided self-made feed for his horses. For the market introduction different activities were necessary. A considerable number of institutes and organizations including the Austrian Armed Forces have investigated, tested and developed these alternative fuels. The increasing disposal problems of used cooking oil have initiated considerations for its use. The recycling of this otherwise waste product, and its preparation for use as an alternative fuel to diesel oil, seems to be most promising.

  8. Phytoremediation of ionic and methyl mercury pollution

    SciTech Connect (OSTI)

    Meagher, R.B.

    1998-06-01

    'The long-term objective of the research is to manipulate single-gene traits into plants, enabling them to process heavy metals and remediate heavy-metal pollution by resistance, sequestration, removal, and management of these contaminants. The authors are focused on mercury pollution as a case study of this plant genetic engineering approach. The working hypothesis behind this proposal was that transgenic plants expressing both the bacterial organo mercury lyase (merB) and the mercuric ion reductase gene (merA) will: (A) remove the mercury from polluted sites and (B) prevent methyl mercury from entering the food chain. The results from the research are so positive that the technology will undoubtedly be applied in the very near future to cleaning large mercury contaminates sites. Many such sites were not remediable previously due to the excessive costs and the negative environmental impact of conventional mechanical-chemical technologies. At the time this grant was awarded 20 months ago, the authors had successfully engineered a small model plant, Arabidopsis thaliana, to use a highly modified bacterial mercuric ion reductase gene, merA9, to detoxify ionic mercury (Hg(II)), reducing it to much less toxic and volatile metallic Hg(0) (Rugh et al., 1996). Seeds from these plants germinate, grow, and set seed at normal growth rates on levels of Hg(II) that are lethal to normal plants. In assays on transgenic seedlings suspended in a solution of Hg(II), 10 ng of Hg(0) was evolved per min per mg wet weight of plant tissue. At that time, the authors had no information on expression of merA in any other plant species, nor had the authors tested merB in any plant. However, the results were so startlingly positive and well received that they clearly presaged a paradigm shift in the field of environmental remediation.'

  9. Properties of some ionic liquids based on1-methyl-3-octylimidazolium and 4-methyl-N-butylpyridinium cations.

    SciTech Connect (OSTI)

    Papaiconomou, Nicolas; Yakelis, Neal; Salminen, Justin; Bergman,Robert; Prausnitz, John M.

    2005-09-29

    Syntheses are reported for ionic liquids containing 1-methyl-3octylimidazolium and 4-methyl-N-butylpyridinium cations, and trifluoromethansulfonate, dicyanamide, bis(trifluoromethylsulfonyl)imide, and nonafluorobutanesulfonate anions. Densities, melting points and glass transition points, solubility in water as well as polarities have been measured. Ionic liquids based on pyridinium cations exhibit higher melting points, lower solubility in water, and higher polarity than those based on imidazolium cations.

  10. APPENDXD.CHP:Corel VENTURA

    Annual Energy Outlook [U.S. Energy Information Administration (EIA)]

    Report The Form EIA-819, "Monthly Oxygenate Report" provides production data for fuel ethanol and methyl tertiary butyl ether (MTBE). End-of-month stock data held at ethanol...

  11. Ethanol Demand in United States Production of Oxygenate-limited Gasoline

    SciTech Connect (OSTI)

    Hadder, G.R.

    2000-08-16

    Ethanol competes with methyl tertiary butyl ether (MTBE) to satisfy oxygen, octane, and volume requirements of certain gasolines. However, MTBE has water quality problems that may create significant market opportunities for ethanol. Oak Ridge National Laboratory (ORNL) has used its Refinery Yield Model to estimate ethanol demand in gasolines with restricted use of MTBE. Reduction of the use of MTBE would increase the costs of gasoline production and possibly reduce the gasoline output of U.S. refineries. The potential gasoline supply problems of an MTBE ban could be mitigated by allowing a modest 3 vol percent MTBE in all gasoline. In the U.S. East and Gulf Coast gasoline producing regions, the 3 vol percent MTBE option results in costs that are 40 percent less than an MTBE ban. In the U.S. Midwest gasoline producing region, with already high use of ethanol, an MTBE ban has minimal effect on ethanol demand unless gasoline producers in other regions bid away the local supply of ethanol. The ethanol/MTBE issue gained momentum in March 2000 when the Clinton Administration announced that it would ask Congress to amend the Clean Air Act to provide the authority to significantly reduce or eliminate the use of MTBE; to ensure that air quality gains are not diminished as MTBE use is reduced; and to replace the existing oxygenate requirement in the Clean Air Act with a renewable fuel standard for all gasoline. Premises for the ORNL study are consistent with the Administration announcement, and the ethanol demand curve estimates of this study can be used to evaluate the impact of the Administration principles and related policy initiatives.

  12. Nested methylation-specific polymerase chain reaction cancer detection method

    DOE Patents [OSTI]

    Belinsky, Steven A.; Palmisano, William A.

    2007-05-08

    A molecular marker-based method for monitoring and detecting cancer in humans. Aberrant methylation of gene promoters is a marker for cancer risk in humans. A two-stage, or "nested" polymerase chain reaction method is disclosed for detecting methylated DNA sequences at sufficiently high levels of sensitivity to permit cancer screening in biological fluid samples, such as sputum, obtained non-invasively. The method is for detecting the aberrant methylation of the p16 gene, O 6-methylguanine-DNA methyltransferase gene, Death-associated protein kinase gene, RAS-associated family 1 gene, or other gene promoters. The method offers a potentially powerful approach to population-based screening for the detection of lung and other cancers.

  13. Geometric and Electronic Structures of the Ni(I) and Methyl-Ni(III)

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

    Intermediates of Methyl-Coenzyme M Reductase 9 Geometric and Electronic Structures of the Ni(I) and Methyl-Ni(III) Intermediates of Methyl-Coenzyme M Reductase Methyl-coenzyme M reductase (MCR) from methanogenic archaea catalyzes the terminal step in biological methane synthesis. Using coenzyme B (CoBSH) as the two-electron donor, MCR reduces methyl-coenzyme M (methyl-SCoM) to form methane and the heterodisulfide product, CoBS-SCoM. MCR contains an essential redox active nickel tetrapyrrolic

  14. Methods for detection of methyl-CpG dinucleotides

    DOE Patents [OSTI]

    Dunn, John J.

    2013-01-29

    The invention provides methods for enriching methyl-CpG sequences from a DNA sample. The method makes use of conversion of cytosine residues to uracil under conditions in which methyl-cytosine residues are preserved. Additional methods of the invention enable to preservation of the context of me-CpG dinucleotides. The invention also provides a recombinant, full length and substantially pure McrA protein (rMcrA) for binding and isolation of DNA fragments containing the sequence 5'-C.sup.MeCpGG-3'. Methods for making and using the rMcrA protein, and derivatives thereof are provided.

  15. Methods for detection of methyl-CpG dinucleotides

    DOE Patents [OSTI]

    Dunn, John J.

    2012-09-11

    The invention provides methods for enriching methyl-CpG sequences from a DNA sample. The method makes use of conversion of cytosine residues to uracil under conditions in which methyl-cytosine residues are preserved. Additional methods of the invention enable to preservation of the context of me-CpG dinucleotides. The invention also provides a recombinant, full length and substantially pure McrA protein (rMcrA) for binding and isolation of DNA fragments containing the sequence 5'-C.sup.MeCpGG-3'. Methods for making and using the rMcrA protein, and derivatives thereof are provided.

  16. Methods for detection of methyl-CpG dinucleotides

    DOE Patents [OSTI]

    Dunn, John J

    2013-11-26

    The invention provides methods for enriching methyl-CpG sequences from a DNA sample. The method makes use of conversion of cytosine residues to uracil under conditions in which methyl-cytosine residues are preserved. Additional methods of the invention enable to preservation of the context of me-CpG dinucleotides. The invention also provides a recombinant, full length and substantially pure McrA protein (rMcrA) for binding and isolation of DNA fragments containing the sequence 5'-C.sup.MeCpGG-3'. Methods for making and using the rMcrA protein, and derivatives thereof are provided.

  17. Low Temperature Autoignition of C8H16O2 Ethyl and Methyl Esters...

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

    Temperature Autoignition of C8H16O2 Ethyl and Methyl Esters in a Motored Engine Low Temperature Autoignition of C8H16O2 Ethyl and Methyl Esters in a Motored Engine qThe alkyl chain ...

  18. Infant sex-specific placental cadmium and DNA methylation associations

    SciTech Connect (OSTI)

    Mohanty, April F.; Farin, Fred M.; Bammler, Theo K.; MacDonald, James W.; Afsharinejad, Zahra; Burbacher, Thomas M.; Siscovick, David S.; and others

    2015-04-15

    Background: Recent evidence suggests that maternal cadmium (Cd) burden and fetal growth associations may vary by fetal sex. However, mechanisms contributing to these differences are unknown. Objectives: Among 24 maternal-infant pairs, we investigated infant sex-specific associations between placental Cd and placental genome-wide DNA methylation. Methods: We used ANOVA models to examine sex-stratified associations of placental Cd (dichotomized into high/low Cd using sex-specific Cd median cutoffs) with DNA methylation at each cytosine-phosphate-guanine site or region. Statistical significance was defined using a false discovery rate cutoff (<0.10). Results: Medians of placental Cd among females and males were 5 and 2 ng/g, respectively. Among females, three sites (near ADP-ribosylation factor-like 9 (ARL9), siah E3 ubiquitin protein ligase family member 3 (SIAH3), and heparin sulfate (glucosamine) 3-O-sulfotransferase 4 (HS3ST4) and one region on chromosome 7 (including carnitine O-octanoyltransferase (CROT) and TP5S target 1 (TP53TG1)) were hypomethylated in high Cd placentas. Among males, high placental Cd was associated with methylation of three sites, two (hypomethylated) near MDS1 and EVI1 complex locus (MECOM) and one (hypermethylated) near spalt-like transcription factor 1 (SALL1), and two regions (both hypomethylated, one on chromosome 3 including MECOM and another on chromosome 8 including rho guanine nucleotide exchange factor (GEF) 10 (ARHGEF10). Differentially methylated sites were at or close to transcription start sites of genes involved in cell damage response (SIAH3, HS3ST4, TP53TG1) in females and cell differentiation, angiogenesis and organ development (MECOM, SALL1) in males. Conclusions: Our preliminary study supports infant sex-specific placental Cd-DNA methylation associations, possibly accounting for previously reported differences in Cd-fetal growth associations across fetal sex. Larger studies are needed to replicate and extend these findings. Such investigations may further our understanding of epigenetic mechanisms underlying maternal Cd burden with suboptimal fetal growth associations. - Highlights: • We examine sex-specific placental-Cd and -genome-wide DNA methylation associations. • In females, associated sites were at/near genes involved in cell damage response. • In males, associated sites were at/near angiogenesis and organ development genes. • Our study supports infant sex-specific placental Cd-DNA methylation associations.

  19. Phase 1 Methyl Iodide Deep-Bed Adsorption Tests

    SciTech Connect (OSTI)

    Nick Soelberg; Tony Watson

    2014-08-01

    Nuclear fission results in the production of fission products (FPs) and activation products including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Research, demonstrations, and some reprocessing plant experience have indicated that diatomic iodine can be captured with efficiencies high enough to meet regulatory requirements. Research on the capture of organic iodides has also been performed, but to a lesser extent [Jubin 2012b]. Several questions remain open regarding the capture of iodine bound in organic compounds. Deep-bed methyl iodide adsorption testing has progressed according to a multi-laboratory methyl iodide adsorption test plan. This report summarizes the first phase of methyl iodide adsorption work performed according to this test plan using the deep-bed iodine adsorption test system at the Idaho National Laboratory (INL), performed during Fiscal Year (FY) 2013 and early FY-2014. Testing has been performed to address questions posed in the test plan, and followed the testing outline in the test plan. Tests established detection limits, developed procedures for sample analysis with minimal analytical interferences, and confirmed earlier results that show that the methyl iodide reacts when in contact with the AgZ sorbent, and not significantly in the gas flow upstream of the sorbent. The reaction(s) enable separation of the iodine from the organic moiety, so that the iodine can chemisorb onto the sorbent. The organic moiety can form other compounds, some of which are organic compounds that are detected and can be tentatively identified using GC-FID and GCMS. Test results also show that other gas constituents (NOx and/or H2O) can affect the methyl iodide reactions. With NOx and H2O present in the gas stream, the majority of uncaptured iodine exiting iodine-laden sorbent beds is in the form of I2 or HI, species that are soluble in NaOH scrubbing solution for iodine analysis. But when NOx and H2O are not present, then the majority of the uncaptured iodine exiting iodine-laden sorbent is in the form of methyl iodide. Methyl iodide adsorption efficiencies have been high enough so that initial DFs exceed 1,000 to 10,000. The methyl iodide mass transfer zone depths are estimated at 4-8 inches, possibly deeper than mass transfer zone depths estimated for I2 adsorption on AgZ. Additional deep-bed testing and analyses are recommended to (a) expand the data base for methyl iodide adsorption under various conditions specified in the methyl iodide test plan, and (b) provide more data for evaluating organic iodide reactions and reaction byproducts for different potential adsorption conditions.

  20. Chemically induced Parkinson's disease: intermediates in the oxidation of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine to the 1-methyl-4-phenyl-pyridinium ion

    SciTech Connect (OSTI)

    Chacon, J.N.; Chedekel, M.R.; Land, E.J.; Truscott, T.G.

    1987-04-29

    Various unstable intermediate oxidation states have been postulated in the metabolic activation of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine to the 1-methyl-4-phenyl pyridinium ion. We now report the first direct observation of these free radical intermediates by pulse radiolysis and flash photolysis. Studies are described of various reactions of such species, in particular with dopamine whose autoxidation to dopamine quinone is reported to be potentiated by 1-methyl-4-phenyl-1,2,3, 6-tetrahydropyridine.

  1. SYNTHESIS OF METHYL METHACRYLATE FROM COAL-DERIVED SYNGAS

    SciTech Connect (OSTI)

    Makarand R. Gogate; James J. Spivey; Joseph R. Zoeller; Richard D. Colberg; Gerald N. Choi; Samuel S. Tam

    1999-04-21

    Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. The research team has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, we are currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. Over the last quarter (January-March/99), in-situ formaldehyde generation and condensation with methyl propionate were tested over various catalysts and reaction conditions. The patent application is in preparation and the results are retained for future reports.

  2. Tropospheric oxidation mechanism of dimethyl ether and methyl formate

    SciTech Connect (OSTI)

    Good, D.A.; Francisco, J.S.

    2000-02-17

    The oxidation mechanism of dimethyl ether is investigated using ab initio methods. The structure and energetics of reactants, products, and transition structures are determined for all pathways involved in the oxidation mechanism. The detailed pathways leading to the experimentally observed products of dimethyl ether oxidation are presented. The energetics of over 50 species and transition structures involved in the oxidation process are calculated with G2 and G2(MP2) energies. The principal pathway following the initial attack of dimethyl ether (CH{sub 3}OCH{sub 3}) by the OH radical is the formation of the methoxymethyl radical (CH{sub 2}OCH{sub 3}). Oxidation steps lead to the formation of methyl formate, which is consistent with the experimentally observed products. Oxidation pathways of methyl formate are also considered.

  3. Synthesis of 6-Methyl-9-n-propyldibenzothiophene-4-ol

    SciTech Connect (OSTI)

    Not Available

    1991-10-28

    The material presented here has been described to some extent in Status Reports 12, 13, and 14 and covers the progress toward the synthesis of the modified target molecules 9-isopropyl-4-methoxy-6-methyldibenzothiophene (13) and 9-isopropyl-6-methyldibenzothiophene-4-ol (14). It is divided into three parts: (a) Dehydrogenation experiments On tetrahydrodibenzothiophene 12. (b) methoxyl methyl cleavage of 13 to 14 using boron tribromide. (c) isolation and purification of methoxydibenzothiophene 13.

  4. FY-2015 Methyl Iodide Deep-Bed Adsorption Test Report

    SciTech Connect (OSTI)

    Soelberg, Nicholas Ray; Watson, Tony Leroy

    2015-09-30

    Nuclear fission produces fission and activation products, including iodine-129, which could evolve into used fuel reprocessing facility off-gas systems, and could require off-gas control to limit air emissions to levels within acceptable emission limits. Deep-bed methyl iodide adsorption testing has continued in Fiscal Year 2015 according to a multi-laboratory methyl iodide adsorption test plan. Updates to the deep-bed test system have also been performed to enable the inclusion of evaporated HNO3 and increased NO2 concentrations in future tests. This report summarizes the result of those activities. Test results showed that iodine adsorption from gaseous methyl iodide using reduced silver zeolite (AgZ) resulted in initial iodine decontamination factors (DFs, ratios of uncontrolled and controlled total iodine levels) under 1,000 for the conditions of the long-duration test performed this year (45 ppm CH3I, 1,000 ppm each NO and NO2, very low H2O levels [3 ppm] in balance air). The mass transfer zone depth exceeded the cumulative 5-inch depth of 4 bed segments, which is deeper than the 2-4 inch depth estimated for the mass transfer zone for adsorbing I2 using AgZ in prior deep-bed tests. The maximum iodine adsorption capacity for the AgZ under the conditions of this test was 6.2% (6.2 g adsorbed I per 100 g sorbent). The maximum Ag utilization was 51%. Additional deep-bed testing and analyses are recommended to (a) expand the data base for methyl iodide adsorption and (b) provide more data for evaluating organic iodide reactions and reaction byproducts for different potential adsorption conditions.

  5. Methyl aryl ethers from coal liquids as gasoline extenders and octane improvers

    SciTech Connect (OSTI)

    Singerman, G.M.

    1980-11-01

    A mixture of methyl aryl ethers derived from the phenols present in direct liquefaction coal liquids shows considerable promise as a gasoline blending agent and octane improver. The mixture of methyl aryl ethers was blended at five volume percent with a commercial, unleaded gasoline. The properties and performance of the blend in a variety of laboratory and automotive tests is reported. The tests show that the mixture of methyl aryl ethers improves gasoline octane without degrading other gasoline properties.

  6. The Structural Basis for Tight Control of PP2A Methylation and Function by

    Office of Scientific and Technical Information (OSTI)

    LCMT-1 (Journal Article) | SciTech Connect The Structural Basis for Tight Control of PP2A Methylation and Function by LCMT-1 Citation Details In-Document Search Title: The Structural Basis for Tight Control of PP2A Methylation and Function by LCMT-1 Proper formation of protein phosphatase 2A (PP2A) holoenzymes is essential for the fitness of all eukaryotic cells. Carboxyl methylation of the PP2A catalytic subunit plays a critical role in regulating holoenzyme assembly; methylation is

  7. Vacuum ultraviolet and infrared spectra of condensed methyl acetate on cold astrochemical dust analogs

    SciTech Connect (OSTI)

    Sivaraman, B.; Nair, B. G.; Mason, N. J.; Lo, J.-I.; Cheng, B.-M.; Kundu, S.; Davis, D.; Prabhudesai, V.; Krishnakumar, E.; Raja Sekhar, B. N.

    2013-12-01

    Following the recent report of the first identification of methyl acetate (CH{sub 3}COOCH{sub 3}) in the interstellar medium (ISM), we have carried out vacuum ultraviolet (VUV) and infrared (IR) spectroscopy studies on methyl acetate from 10 K until sublimation in an ultrahigh vacuum chamber simulating astrochemical conditions. We present the first VUV and IR spectra of methyl acetate relevant to ISM conditions. Spectral signatures clearly showed molecular reorientation to have started in the ice by annealing the amorphous ice formed at 10 K. An irreversible phase change from amorphous to crystalline methyl acetate ice was found to occur between 110 K and 120 K.

  8. Exploring the roles of DNA methylation in the metal-reducing bacterium Shewanella oneidensis MR-1

    SciTech Connect (OSTI)

    Bendall, Matthew L.; Luong, Khai; Wetmore, Kelly M.; Blow, Matthew; Korlach, Jonas; Deutschbauer, Adam; Malmstrom, Rex

    2013-08-30

    We performed whole genome analyses of DNA methylation in Shewanella 17 oneidensis MR-1 to examine its possible role in regulating gene expression and 18 other cellular processes. Single-Molecule Real Time (SMRT) sequencing 19 revealed extensive methylation of adenine (N6mA) throughout the 20 genome. These methylated bases were located in five sequence motifs, 21 including three novel targets for Type I restriction/modification enzymes. The 22 sequence motifs targeted by putative methyltranferases were determined via 23 SMRT sequencing of gene knockout mutants. In addition, we found S. 24 oneidensis MR-1 cultures grown under various culture conditions displayed 25 different DNA methylation patterns. However, the small number of differentially 26 methylated sites could not be directly linked to the much larger number of 27 differentially expressed genes in these conditions, suggesting DNA methylation is 28 not a major regulator of gene expression in S. oneidensis MR-1. The enrichment 29 of methylated GATC motifs in the origin of replication indicate DNA methylation 30 may regulate genome replication in a manner similar to that seen in Escherichia 31 coli. Furthermore, comparative analyses suggest that many 32 Gammaproteobacteria, including all members of the Shewanellaceae family, may 33 also utilize DNA methylation to regulate genome replication.

  9. Unexpected methyl migrations of ethanol dimer under synchrotron VUV radiation

    SciTech Connect (OSTI)

    Xiao, Weizhan; Hu, Yongjun E-mail: lssheng@ustc.edu.cn; Li, Weixing; Guan, Jiwen; Liu, Fuyi; Shan, Xiaobin; Sheng, Liusi E-mail: lssheng@ustc.edu.cn

    2015-01-14

    While methyl transfer is well known to occur in the enzyme- and metal-catalyzed reactions, the methyl transfer in the metal-free organic molecules induced by the photon ionization has been less concerned. Herein, vacuum ultraviolet single photon ionization and dissociation of ethanol dimer are investigated with synchrotron radiation photoionization mass spectroscopy and theoretical methods. Besides the protonated clusters cation (C{sub 2}H{sub 5}OH) ⋅ H{sup +} (m/z = 47) and the β-carbon-carbon bond cleavage fragment CH{sub 2}O ⋅ (C{sub 2}H{sub 5}OH)H{sup +} (m/z = 77), the measured mass spectra revealed that a new fragment (C{sub 2}H{sub 5}OH) ⋅ (CH{sub 3}){sup +} (m/z = 61) appeared at the photon energy of 12.1 and 15.0 eV, where the neutral dimer could be vertically ionized to higher ionic state. Thereafter, the generated carbonium ions are followed by a Wagner-Meerwein rearrangement and then dissociate to produce this new fragment, which is considered to generate after surmounting a few barriers including intra- and inter-molecular methyl migrations by the aid of theoretical calculations. The appearance energy of this new fragment is measured as 11.55 ± 0.05 eV by scanning photoionization efficiency curve. While the signal intensity of fragment m/z = 61 starts to increase, the fragments m/z = 47 and 77 tend to slowly incline around 11.55 eV photon energy. This suggests that the additional fragment channels other than (C{sub 2}H{sub 5}OH) ⋅ H{sup +} and CH{sub 2}O ⋅ (C{sub 2}H{sub 5}OH)H{sup +} have also been opened, which consume some dimer cations. The present report provides a clear description of the photoionization and dissociation processes of the ethanol dimer in the range of the photon energy 12-15 eV.

  10. High Temperature Chemical Kinetic Combustion Modeling of Lightly Methylated Alkanes

    SciTech Connect (OSTI)

    Sarathy, S M; Westbrook, C K; Pitz, W J; Mehl, M

    2011-03-01

    Conventional petroleum jet and diesel fuels, as well as alternative Fischer-Tropsch (FT) fuels and hydrotreated renewable jet (HRJ) fuels, contain high molecular weight lightly branched alkanes (i.e., methylalkanes) and straight chain alkanes (n-alkanes). Improving the combustion of these fuels in practical applications requires a fundamental understanding of large hydrocarbon combustion chemistry. This research project presents a detailed high temperature chemical kinetic mechanism for n-octane and three lightly branched isomers octane (i.e., 2-methylheptane, 3-methylheptane, and 2,5-dimethylhexane). The model is validated against experimental data from a variety of fundamental combustion devices. This new model is used to show how the location and number of methyl branches affects fuel reactivity including laminar flame speed and species formation.

  11. Methyl-CpG island-associated genome signature tags

    DOE Patents [OSTI]

    Dunn, John J

    2014-05-20

    Disclosed is a method for analyzing the organismic complexity of a sample through analysis of the nucleic acid in the sample. In the disclosed method, through a series of steps, including digestion with a type II restriction enzyme, ligation of capture adapters and linkers and digestion with a type IIS restriction enzyme, genome signature tags are produced. The sequences of a statistically significant number of the signature tags are determined and the sequences are used to identify and quantify the organisms in the sample. Various embodiments of the invention described herein include methods for using single point genome signature tags to analyze the related families present in a sample, methods for analyzing sequences associated with hyper- and hypo-methylated CpG islands, methods for visualizing organismic complexity change in a sampling location over time and methods for generating the genome signature tag profile of a sample of fragmented DNA.

  12. Global prevalence and distribution of genes and microorganisms involved in mercury methylation

    SciTech Connect (OSTI)

    Podar, Mircea; Gilmour, C C; Brandt, Craig C; Bullock, Allyson L; Brown, Steven D; Crable, Bryan R; Palumbo, Anthony Vito; Somenahally, Anil C; Elias, Dwayne A

    2015-01-01

    Mercury methylation produces the neurotoxic, highly bioaccumulative methylmercury (MeHg). Recent identification of the methylation genes (hgcAB) provides the foundation for broadly evaluating microbial Hg-methylation potential in nature without making explicit rate measurements. We queried hgcAB diversity and distribution in all available microbial metagenomes, encompassing most environments. The genes were found in nearly all anaerobic, but not in aerobic, environments including oxygenated layers of the open ocean. Critically, hgcAB was effectively absent in ~1500 human microbiomes, suggesting a low risk of endogenous MeHg production. New potential methylation habitats were identified, including invertebrate guts, thawing permafrost, coastal dead zones , soils, sediments, and extreme environments, suggesting multiple routes for MeHg entry into food webs. Several new taxonomic groups potentially capable of Hg-methylation emerged, including lineages having no cultured representatives. We begin to address long-standing evolutionary questions about Hg-methylation and ancient carbon fixation mechanisms while generating a new global view of Hg-methylation potential.

  13. Global prevalence and distribution of genes and microorganisms involved in mercury methylation

    SciTech Connect (OSTI)

    Podar, Mircea; Gilmour, C. C.; Brandt, Craig C.; Soren, Allyson; Brown, Steven D.; Crable, Bryan R.; Palumbo, Anthony Vito; Somenahally, Anil C.; Elias, Dwayne A.

    2015-01-01

    Mercury methylation produces the neurotoxic, highly bioaccumulative methylmercury (MeHg). Recent identification of the methylation genes (hgcAB) provides the foundation for broadly evaluating microbial Hg-methylation potential in nature without making explicit rate measurements. We first queried hgcAB diversity and distribution in all available microbial metagenomes, encompassing most environments. The genes were found in nearly all anaerobic, but not in aerobic, environments including oxygenated layers of the open ocean. Critically, hgcAB was effectively absent in ~1500 human microbiomes, suggesting a low risk of endogenous MeHg production. New potential methylation habitats were identified, including invertebrate guts, thawing permafrost, coastal dead zones, soils, sediments, and extreme environments, suggesting multiple routes for MeHg entry into food webs. Several new taxonomic groups potentially capable of Hg-methylation emerged, including lineages having no cultured representatives. We then begin to address long-standing evolutionary questions about Hg-methylation and ancient carbon fixation mechanisms while generating a new global view of Hg-methylation potential.

  14. SYNTHESIS OF METHYL METHACRYLATE FROM COAL-DERIVED SYNGAS

    SciTech Connect (OSTI)

    BEN W.-L. JANG; GERALD N. CHOI; JAMES J. SPIVEY; JOSPEH R. ZOELLER; RICHARD D. COLBERG

    1999-01-20

    Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. The research team has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, we are currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. Over the last quarter(Oct.-Dec./98), we have investigated the condensation between methyl propionate and formaldehyde (MP/HCHO=4.5/1) at various reaction temperatures(280-360EC) over 5%, 10%, and 20% Nb O /SiO catalysts. The conversion of HCHO increases with reaction 2 5 2 temperature and niobium loading. MMA+MAA selectivity goes through a maximum with the temperature over both 10% and 20% Nb O /SiO . The selectivities to MMA+MAA are 67.2%, 2 5 2 72.3%and 58.1% at 320EC over 5%, 10%, 20% Nb O /SiO , respectively. However, the 2 5 2 conversion of formaldehyde decreases rapidly with time on stream. The results suggest that silica supported niobium catalysts are active and selective for condensation of MP with HCHO, but deactivation needs to be minimized for the consideration of commercial application. We have preliminarily investigated the partial oxidation of dimethyl ether(DME) over 5% Nb O /SiO catalyst. Reactant gas mixture of 0.1% DME, 0.1% O and balance nitrogen is 2 5 2 2 studied with temperature ranging from 200°C to 500°C. The conversion of DME first increases with temperature reaching an maximum at 400°C then decreases. The selectivity to HCHO also increases with reaction temperature first. But the selectivity to HCHO decreases at temperature above 350°C accompanied by the increasing selectivity to CO . The results suggest that silica 2 supported niobium catalysts are active for partial oxidation of DME to HCHO. Best temperatures for partial oxidation are between 300 and 400°C. A short paper submitted to the ACS National Meeting at Anaheim(March 1999) was accepted for oral presentation. The title is �Catalytic Synthesis of Methacrylates over Silica Supported Niobium Catalysts� and will appear in the ACS preprints.

  15. SYNTHESIS OF METHYL METHACRYLATE FROM COAL-DERIVED SYNGAS

    SciTech Connect (OSTI)

    Makarand R. Gogate; James J. Spivey; Joseph R. Zoeller; Richard D. Colberg; Gerald N. Choi

    1999-07-19

    Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. The research team has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, we are currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. During the April-June quarter(04-06/99) the first in-situ formaldehyde generation from DME and condensation with methyl propionate is demonstrated and the results are summarized. The supported niobium catalyst shows better condensation activity, but supported tungsten catalyst has higher formaldehyde selectivity. The project team has also completed a 200-hour long term test of PA-HCHO condensation over 30% Nb{sub 2}O{sub 5}/SiO{sub 2}. Three activity cycles and two regeneration cycles were carried out. 30% Nb{sub 2}O{sub 5}/SiO{sub 2} showed similar MAA yields as 10% Nb{sub 2}O{sub 5}/SiO{sub 2} at 300 C. However, the deactivation appears to be slower with 30% Nb{sub 2}O{sub 5}/SiO{sub 2} than 10% Nb{sub 2}O{sub 5}/SiO{sub 2}. An detailed economic analysis of PA-HCHO condensation process for a 250 million lb/yr MMA plant is currently studied by Bechtel. Using the Amoco data-based azeotropic distillation model as the basis, an ASPEN flow sheet model was constructed to simulate the formaldehyde and propionic acid condensation processing section based on RTI's design data. The RTI MAA effluent azeotropic distillation column was found to be much more difficult to converge. The presence of non-condensible gases along with the byproduct DEK (both of which were not presented in Amoco's data) appear to the culprits.

  16. Thermochemistry of C-O, (CO)-O, and (CO)-C bond breaking in fatty acid methyl esters

    SciTech Connect (OSTI)

    Osmont, Antoine; Yahyaoui, Mohammed; Catoire, Laurent; Goekalp, Iskender; Swihart, Mark T.

    2008-10-15

    Density functional theory quantum chemical calculations corrected with empirical atomic increments have been used to examine C-O, (CO)-O, and (CO)-C bond scission enthalpies in gas-phase fatty acid methyl esters (FAMEs) present in biodiesel derived from rapeseed oil methyl ester and soybean oil methyl ester. Mechanistic information, currently not available elsewhere for these large species, is obtained based on thermochemical considerations and compared to thermochemical considerations reported for methyl butanoate, a small methyl ester sometimes used as a model for FAMEs. These results are compared to previously reported C-C and C-H bond scissions in these FAMEs, derived using this same protocol. (author)

  17. Synthesis of Methyl Methacrylate from Coal-Derived Syngas

    SciTech Connect (OSTI)

    Gerald N. Choi; James J. Spivey; Jospeh R. Zoeller; Makarand R. Gogate; Richard D. Colberg; Samuel S. Tam

    1998-04-17

    Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. RTI has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, RTI is currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. Over the last month, RTI has finalized the design of a fixed-bed microreactor system for DME partial oxidation reactions. RTI incorporated some design changes to the feed blending system, so as to be able to blend varying proportions of DME and oxygen. RTI has also examined the flammability limits of DME-air mixtures. Since the lower flammability limit of DME in air is 3.6 volume percent, RTI will use a nominal feed composition of 1.6 percent in air, which is less than half the lower explosion limit for DME-air mixtures. This nominal feed composition is thus considered operationally safe, for DME partial oxidation reactions. RTI is also currently developing an analytical system for DME partial oxidation reaction system.

  18. Optimized End-Stacking Provides Specificity of N-Methyl Mesoporphyrin...

    Office of Scientific and Technical Information (OSTI)

    Optimized End-Stacking Provides Specificity of N-Methyl Mesoporphyrin IX for Human Telomeric G-Quadruplex DNA Citation Details In-Document Search Title: Optimized End-Stacking ...

  19. The Structural Basis for Tight Control of PP2A Methylation and...

    Office of Scientific and Technical Information (OSTI)

    The Structural Basis for Tight Control of PP2A Methylation and Function by LCMT-1 Citation Details In-Document Search Title: The Structural Basis for Tight Control of PP2A ...

  20. Effects of nickel, chromate, and arsenite on histone 3 lysine methylation

    Office of Scientific and Technical Information (OSTI)

    (Journal Article) | SciTech Connect Effects of nickel, chromate, and arsenite on histone 3 lysine methylation Citation Details In-Document Search Title: Effects of nickel, chromate, and arsenite on histone 3 lysine methylation Occupational exposure to nickel (Ni), chromium (Cr), and arsenic (As) containing compounds has been associated with lung cancer and other adverse health effects. Their carcinogenic properties may be attributable in part, to activation and/or repression of gene

  1. Modulation of histone methylation and MLH1 gene silencing by hexavalent

    Office of Scientific and Technical Information (OSTI)

    chromium (Journal Article) | SciTech Connect Modulation of histone methylation and MLH1 gene silencing by hexavalent chromium Citation Details In-Document Search Title: Modulation of histone methylation and MLH1 gene silencing by hexavalent chromium Hexavalent chromium [Cr(VI)] is a mutagen and carcinogen, and occupational exposure can lead to lung cancers and other adverse health effects. Genetic changes resulting from DNA damage have been proposed as an important mechanism that mediates

  2. Optimized End-Stacking Provides Specificity of N-Methyl Mesoporphyrin IX

    Office of Scientific and Technical Information (OSTI)

    for Human Telomeric G-Quadruplex DNA (Journal Article) | SciTech Connect Optimized End-Stacking Provides Specificity of N-Methyl Mesoporphyrin IX for Human Telomeric G-Quadruplex DNA Citation Details In-Document Search Title: Optimized End-Stacking Provides Specificity of N-Methyl Mesoporphyrin IX for Human Telomeric G-Quadruplex DNA Authors: Nicoludis, John M. ; Miller, Stephen T. ; Jeffrey, Philip D. ; Barrett, Steven P. ; Rablen, Paul R. ; Lawton, Thomas J. ; Yatsunyk, Liliya A. [1] ;

  3. Radio-methyl vorozole and methods for making and using the same

    DOE Patents [OSTI]

    Kim, Sung Won; Biegon, Anat; Fowler, Joanna S.

    2014-08-05

    Radiotracer vorozole compounds for in vivo and in vitro assaying, studying and imaging cytochrome P450 aromatase enzymes in humans, animals, and tissues and methods for making and using the same are provided. [N-radio-methyl] vorozole substantially separated from an N-3 radio-methyl isomer of vorozole is provided. Separation is accomplished through use of chromatography resins providing multiple mechanisms of selectivity.

  4. Radio-methyl vorozole and methods for making and using the same

    DOE Patents [OSTI]

    Kim, Sung Won; Biegon, Anat; Fowler, Joanna S.

    2014-08-12

    Radiotracer vorozole compounds for in vivo and in vitro assaying, studying and imaging cytochrome P450 aromatase enzymes in humans, animals, and tissues and methods for making and using the same are provided. [N-radio-methyl] vorozole substantially separated from an N-3 radio-methyl isomer of vorozole is provided. Separation is accomplished through use of chromatography resins providing multiple mechanisms of selectivity.

  5. Determination of Total Lipids as Fatty Acid Methyl Esters (FAME) by in situ

    Office of Scientific and Technical Information (OSTI)

    Transesterification: Laboratory Analytical Procedure (LAP) (Technical Report) | SciTech Connect Determination of Total Lipids as Fatty Acid Methyl Esters (FAME) by in situ Transesterification: Laboratory Analytical Procedure (LAP) Citation Details In-Document Search Title: Determination of Total Lipids as Fatty Acid Methyl Esters (FAME) by in situ Transesterification: Laboratory Analytical Procedure (LAP) This procedure is based on a whole biomass transesterification of lipids to fatty acid

  6. Experimental and Kinetic Modeling Study of Extinction and Ignition of Methyl Decanoate in Laminar Nonpremixed Flows

    SciTech Connect (OSTI)

    Seshadri, K; Lu, T; Herbinet, O; Humer, S; Niemann, U; Pitz, W J; Law, C K

    2008-01-09

    Methyl decanoate is a large methyl ester that can be used as a surrogate for biodiesel. In this experimental and computational study, the combustion of methyl decanoate is investigated in nonpremixed, nonuniform flows. Experiments are performed employing the counterflow configuration with a fuel stream made up of vaporized methyl decanoate and nitrogen, and an oxidizer stream of air. The mass fraction of fuel in the fuel stream is measured as a function of the strain rate at extinction, and critical conditions of ignition are measured in terms of the temperature of the oxidizer stream as a function of the strain rate. It is not possible to use a fully detailed mechanism for methyl decanoate to simulate the counterflow flames because the number of species and reactions is too large to employ with current flame codes and computer resources. Therefore a skeletal mechanism was deduced from a detailed mechanism of 8555 elementary reactions and 3036 species using 'directed relation graph' method. This skeletal mechanism has only 713 elementary reactions and 125 species. Critical conditions of ignition were calculated using this skeletal mechanism and are found to agree well with experimental data. The predicted strain rate at extinction is found to be lower than the measurements. In general, the methyl decanoate mechanism provides a realistic kinetic tool for simulation of biodiesel fuels.

  7. Synthesis of Methyl Methacrylate From Coal-Derived Syngas

    SciTech Connect (OSTI)

    Ben W.-L. Jang; Gerald N. Choi; James J. Spivey; Jospeh R. Zoeller; Richard D. Colberg; Samuel S. Tam

    1998-07-27

    Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. RTI has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, RTI is currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. Over the last quarter(April-June, 1998), RTI has modified the reactor system including a new preheater and new temperature settings for the preheater. Continuous condensation of formaldehyde with propionic acid were carried out over 10% Nb O /SiO at 300°C without 2 5 2 interruption. Five activity and four regeneration cycles have been completed without plugging or material balance problems. The results show that 10% Nb O /SiO deactivates slowly with time 2 5 2 but can be regenerated, at least four times, to 100% of its original activity with 2% O in nitrogen 2 at 400°C. The cycles continue with consistent 90-95% of carbon balance. The reaction is scheduled to complete with 6 activity cycles and 5 regenerations. Used catalysts will be analyzed with TGA and XPS to determine bulk and surface coke content and coke properties. RTI will start the investigation of effects of propionic acid/formaldehyde ratio on reaction activity and product selectivity over 20% Nb O /SiO catalysts.

  8. Vapor pressures of methyl tert-butyl ether, ethyl tert-butyl ether, isopropyl tert-butyl ether, tert-amyl methyl ether, and tert-amyl ethyl ether

    SciTech Connect (OSTI)

    Kraehenbuehl, M.A.; Gmehling, J. . Technische Chemie)

    1994-10-01

    The vapor pressures of methyl tert-butyl ether, ethyl tert-butyl ether, isopropyl tert-butyl ether, tert-amyl methyl ether, and tert-amyl ethyl ether were measured by ebulliometry or the static method in the pressure ranges 14--102 and 3--835 kPa (methyl tert-butyl ether), respectively. The data were correlated using the Antoine and Wagner equations. The experimental data of methyl tert-butyl ether and ethyl tert-butyl ether were compared with data available in the literature.

  9. SYNTHESIS OF METHYL METHACRYLATE FROM COAL-DERIVED SYNGAS

    SciTech Connect (OSTI)

    BEN W.-L. JANG; GERALD N. CHOI; JAMES J. SPIVEY; JOSPEH R. ZOELLER; RICHARD D. COLBERG

    1998-10-20

    Research Triangle Institute (RTI), Eastman Chemical Company, and Bechtel collectively are developing a novel three-step process for the synthesis of methyl methacrylate (MMA) from coal-derived syngas that consists of the steps of synthesis of a propionate, its condensation with formaldehyde to form methacrylic acid (MAA), and esterification of MAA with methanol to produce MMA. RTI has completed the research on the three-step methanol-based route to MMA. Under an extension to the original contract, RTI is currently evaluating a new DME-based process for MMA. The key research need for DME route is to develop catalysts for DME partial oxidation reactions and DME condensation reactions. Over the last quarter (July-September, 1998), the project team has completed the continuous condensation of formaldehyde with propionic acid over 10% Nb{sub 2}O{sub 5}/SiO{sub 2} at 300 C. Six activity and five regeneration cycles have been completed. The results show that 10% Nb{sub 2}O{sub 5}/SiO{sub 2} deactivates slowly with time but can be regenerated to its original activity with 2% O{sub 2} in nitrogen over night at 400 C. We have investigated the effects of regeneration, propionic acid/formaldehyde ratio (PA/HCHO = 4.5/1 to 1.5/1) and reaction temperature(280-300 C) on reaction activity and product selectivity over 20% Nb{sub 2}O{sub 5}/SiO{sub 2} catalysts. The regeneration effect on 20% Nb{sub 2}O{sub 5}/SiO{sub 2} is similar to the effect on 10% Nb{sub 2}O{sub 5}/SiO{sub 2}. The regeneration can bring the deactivated catalyst to its original activity. However, the selectivity to MAA decreases with regeneration while the selectivity to DEK and CO{sub 2} increases. When PA/HCHO ratio is decreased from 4.5/1 to 2.25/1 then to 1.5/1 at 300 C the MAA yield decreases but the MAA selectivity first increases then decreases. Decreasing the reaction temperature from 300 C to 280 C decreases the MAA yield from 39.5% to 30.7% but increases the MAA selectivity from 73.7% to 82.2%. The results indicate that both temperature and PA/HCHO ratio are important parameters to optimize the economic of the condensation between propionic acid and formaldehyde.

  10. Synthesis Of [2h, 13c] And [2h3, 13c]Methyl Aryl Sulfides

    DOE Patents [OSTI]

    Martinez, Rodolfo A.; Alvarez, Marc A.; Silks, III, Louis A.; Unkefer, Clifford J.

    2004-03-30

    The present invention is directed to labeled compounds, [.sup.2 H.sub.1, .sup.13 C], [.sup.2 H.sub.2, .sup.13 C] and [.sup.2 H.sub.3, .sup.13 C]methyl aryl sulfides wherein the .sup.13 C methyl group attached to the sulfur of the sulfide includes exactly one, two or three deuterium atoms and the aryl group is selected from the group consisting of 1-naphthyl, substituted 1-naphthyl, 2-naphthyl, substituted 2-naphthyl, and phenyl groups with the structure ##STR1## wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, and R.sub.5 are each independently, hydrogen, a C.sub.1 -C.sub.4 lower alkyl, a halogen, an amino group from the group consisting of NH.sub.2, NHR and NRR' where R and R' are each a C.sub.1 -C.sub.4 lower alkyl, a phenyl, or an alkoxy group. The present invention is also directed to processes of preparing [.sup.2 H.sub.1, .sup.13 C], [.sup.2 H.sub.2,.sup.13 C] and [.sup.2 H.sub.3, .sup.13 C]methyl aryl sulfides wherein the .sup.13 C methyl group attached to the sulfur of the sulfide includes exactly one, two or three deuterium atoms. The present invention is also directed to the labeled compounds of [.sup.2 H.sub.1, .sup.13 C]methyl iodide and [.sup.2 H.sub.2, .sup.13 C]methyl iodide.

  11. Polylactide?Poly(6-methyl-[espilson]-caprolactone)?Polylactide Thermoplastic Elastomers

    SciTech Connect (OSTI)

    Martello, Mark T.; Hillmyer, Marc A.

    2012-11-14

    Amorphous ABA type block aliphatic polyesters can be useful as degradable and biorenewable thermoplastic elastomers. These materials can be prepared by sequential ring-opening transesterification polymerization (ROTEP) reactions and can exhibit a range of physical properties and morphologies. In this work a set of amorphous polylactide-poly(6-methyl-{epsilon}-caprolactone)-polylactide aliphatic polyester ABA triblock copolymers were prepared by consecutive controlled ring-opening polymerizations. Ring-opening polymerization of neat 6-methyl-{epsilon}-caprolactone in the presence of 1,4-benzenedimethanol and tin(II) octoate afforded {alpha},{omega}-hydroxyl-terminated poly(6-methyl-{epsilon}-caprolactone). High conversions of 6-methyl-{epsilon}-caprolactone (>96%) afforded polymers with molar masses ranging from 12 to 98 kg mol{sup -1}, depending on monomer-to-initiator ratios, polymers with narrow, monomodal molecular weight distributions. An array of polylactide-poly(6-methyl-{epsilon}-caprolactone)-polylactide triblock copolymers with controlled molecular weights and narrow molecular weight distributions were synthesized using the telechelic poly(6-methyl-{epsilon}-caprolactone) samples as macroinitiators for the ring-opening polymerization of D,L-lactide. The morphological, thermal, and mechanical behaviors of these materials were explored. Several triblocks adopted well-ordered microphase-separated morphologies, and both hexagonally packed cylindrical and lamellar structures were observed. The Flory-Huggins interaction parameter was determined, x(T) = 61.2 T{sup -1} - 0.1, based on the order-to-disorder transition temperatures of two symmetric triblocks using the calculated mean field theory result. The elastomeric mechanical behavior of two high molecular weight triblocks was characterized by tensile and elastic recovery experiments.

  12. The role of DNA methylation in catechol-enhanced erythroid differentiation of K562 cells

    SciTech Connect (OSTI)

    Li, Xiao-Fei; Wu, Xiao-Rong; Xue, Ming; Wang, Yan; Wang, Jie; Li, Yang; Suriguga,; Zhang, Guang-Yao; Yi, Zong-Chun

    2012-11-15

    Catechol is one of phenolic metabolites of benzene in vivo. Catechol is also widely used in pharmaceutical and chemical industries. In addition, fruits, vegetables and cigarette smoke also contain catechol. Our precious study showed that several benzene metabolites (phenol, hydroquinone, and 1,2,4-benzenetriol) inhibited erythroid differentiation of K562 cells. In present study, the effect of catechol on erythroid differentiation of K562 cells was investigated. Moreover, to address the role of DNA methylation in catechol-induced effect on erythroid differentiation in K562 cells, methylation levels of erythroid-specific genes were analyzed by Quantitative MassARRAY methylation analysis platform. Benzidine staining showed that exposure to catechol enhanced hemin-induced hemoglobin accumulation in K562 cells in concentration- and time-dependent manners. The mRNA expression of erythroid specific genes, including ?-globin, ?-globin, ?-globin, erythroid 5-aminolevulinate synthase, erythroid porphobilinogen deaminase, and transcription factor GATA-1 genes, showed a significant concentration-dependent increase in catechol-treated K562 cells. The exposure to catechol caused a decrease in DNA methylation levels at a few CpG sites in some erythroid specific genes including ?-globin, ?-globin and erythroid porphobilinogen deaminase genes. These results indicated that catechol improved erythroid differentiation potency of K562 cells at least partly via up-regulating transcription of some erythroid related genes, and suggested that inhibition of DNA methylation might be involved in up-regulated expression of some erythroid related genes. -- Highlights: ? Catechol enhanced hemin-induced hemoglobin accumulation. ? Exposure to catechol resulted in up-regulated expression of erythroid genes. ? Catechol reduced methylation levels at some CpG sites in erythroid genes.

  13. Experimental study of the oxidation of methyl oleate in a jet-stirred reactor

    SciTech Connect (OSTI)

    Bax, Sarah; Hakka, Mohammed Hichem; Glaude, Pierre-Alexandre; Herbinet, Olivier; Battin-Leclerc, Frederique

    2010-06-15

    The experimental study of the oxidation of a blend containing n-decane and a large unsaturated ester, methyl oleate, was performed in a jet-stirred reactor over a wide range of temperature covering both low and high temperature regions (550-1100 K), at a residence time of 1.5 s, at quasi atmospheric pressure with high dilution in helium (n-decane and methyl oleate inlet mole fractions of 1.48 x 10{sup -3} and 5.2 x 10{sup -4}) and under stoichiometric conditions. The formation of numerous reaction products was observed. At low and intermediate temperatures, the oxidation of the blend led to the formation of species containing oxygen atoms like cyclic ethers, aldehydes and ketones deriving from n-decane and methyl oleate. At higher temperature, these species were not formed anymore and the presence of unsaturated species was observed. Because of the presence of the double bond in the middle of the alkyl chain of methyl oleate, the formation of some specific products was observed. These species are dienes and esters with two double bonds produced from the decomposition paths of methyl oleate and some species obtained from the addition of H-atoms, OH and HO{sub 2} radicals to the double bond. Experimental results were compared with former results of the oxidation of a blend of n-decane and methyl palmitate performed under similar conditions. This comparison allowed highlighting the similarities and the differences in the reactivity and in the distribution of the reaction products for the oxidation of large saturated and unsaturated esters. (author)

  14. Crystal structure of 1-methyl-3-([2,2-dimethyl-4,6-dioxo-1,3-dioxane-5-ylidene]methyl)urea

    SciTech Connect (OSTI)

    Habibi, A. Ghorbani, H. S.; Bruno, G.; Rudbari, H. A.; Valizadeh, Y.

    2013-12-15

    The crystal structure of 1-Methyl-3-([2,2-dimethyl-4,6-dioxo-1,3-dioxane-5-ylidene]methyl)urea (C{sub 9}H{sub 12}N{sub 2}O{sub 5}) has been determined by single crystal X-ray diffraction analysis. The crystals are monoclinic, a = 5.3179(2), b = 18.6394(6), c =10.8124(3) , ? = 100.015(2), Z = 4, sp. gr. P2{sub 1}/c, R = 0.0381 for 2537 reflections with I > 2?(I). Except for C(CH{sub 3}){sub 2} group, the molecule is planar. The structure is stabilized by inter- and intramolecular N-H...O hydrogen bonds and weak C-H...O interactions.

  15. Acute environmental toxicity and persistence of methyl salicylate: A chemical agent simulant. Final report

    SciTech Connect (OSTI)

    Cataldo, D.A.; Ligotke, M.W.; Harvey, S.D.; Fellows, R.J.; Li, S.W.

    1994-06-01

    The interactions of methyl salicylate with plant foliage and soils were assessed using aerosol/vapor exposure methods. Measurements of deposition velocity and residence times for soils and foliar surfaces are reported. Severe plant contact toxicity was observed at foliar mass-loading levels above 4 {mu}g/cm{sup 2} leaf; however, recovery was noted after four to fourteen days. Methyl salicylate has a short-term effect on soil dehydrogenase activity, but not phosphatase activity. Results of the earthworm bioassay indicated only minimal effects on survival.

  16. Enhanced diisobutene production in the presence of methyl tertiary butyl ether

    DOE Patents [OSTI]

    Smith, L.A. Jr.

    1983-03-01

    In the liquid phase reaction of isobutene in the presence of resin cation exchange resins with itself in a C[sub 4] hydrocarbon stream to form dimers, the formation of higher polymers, oligomers, and co-dimer by-products is suppressed by the presence of 0.0001 to 1 mole per mole of isobutene of methyl tertiary butyl ether. 1 fig.

  17. Enhanced diisobutene production in the presence of methyl tertiary butyl ether

    DOE Patents [OSTI]

    Smith, Jr., Lawrence A. (Bellaire, TX)

    1983-01-01

    In the liquid phase reaction of isobutene in the presence of resin cation exchange resins with itself in a C.sub.4 hydrocarbon stream to form dimers, the formation of higher polymers, oligomers, and co-dimer by-products is suppressed by the presence of 0.0001 to 1 mole per mole of isobutene of methyl tertiary butyl ether.

  18. Hydrogen-terminated silicon nanowire photocatalysis: Benzene oxidation and methyl red decomposition

    SciTech Connect (OSTI)

    Lian, Suoyuan; School of Chemical Engineering and Materials, Dalian Polytechnic University, Dalian 116034 ; Tsang, Chi Him A.; Centre of Super Diamond and Advanced Films, City University of Hong Kong, Hong Kong ; Kang, Zhenhui; Liu, Yang; Wong, Ningbew; Lee, Shuit-Tong; Centre of Super Diamond and Advanced Films, City University of Hong Kong, Hong Kong

    2011-12-15

    Graphical abstract: H-SiNWs can catalyze hydroxylation of benzene and degradation of methyl red under visible light irradiation. Highlights: Black-Right-Pointing-Pointer Hydrogen-terminated silicon nanowires were active photocatalyst in the hydroxylation of benzene under light. Black-Right-Pointing-Pointer Hydrogen-terminated silicon nanowires were also effective in the decomposition of methyl red dye. Black-Right-Pointing-Pointer The Si/SiO{sub x} core-shell structure is the main reason of the obtained high selectivity during the hydroxylation. -- Abstract: Hydrogen-terminated silicon nanowires (H-SiNWs) were used as heterogeneous photocatalysts for the hydroxylation of benzene and for the decomposition of methyl red under visible light irradiation. The above reactions were monitored by GC-MS and UV-Vis spectrophotometry, respectively, which shows 100% selectivity for the transformation of benzene to phenol. A complete decomposition of a 2 Multiplication-Sign 10{sup -4} M methyl red solution was achieved within 30 min. The high selectivity for the hydroxylation of benzene and the photodecomposition demonstrate the catalytic activity of ultrafine H-SiNWs during nanocatalysis.

  19. Impaired methylation as a novel mechanism for proteasome suppression in liver cells

    SciTech Connect (OSTI)

    Osna, Natalia A.; White, Ronda L.; Donohue, Terrence M.; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68105 ; Beard, Michael R.; Tuma, Dean J.; Kharbanda, Kusum K.; Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68105

    2010-01-08

    The proteasome is a multi-catalytic protein degradation enzyme that is regulated by ethanol-induced oxidative stress; such suppression is attributed to CYP2E1-generated metabolites. However, under certain conditions, it appears that in addition to oxidative stress, other mechanisms are also involved in proteasome regulation. This study investigated whether impaired protein methylation that occurs during exposure of liver cells to ethanol, may contribute to suppression of proteasome activity. We measured the chymotrypsin-like proteasome activity in Huh7CYP cells, hepatocytes, liver cytosols and nuclear extracts or purified 20S proteasome under conditions that maintain or prevent protein methylation. Reduction of proteasome activity of hepatoma cell and hepatocytes by ethanol or tubercidin was prevented by simultaneous treatment with S-adenosylmethionine (SAM). Moreover, the tubercidin-induced decline in proteasome activity occurred in both nuclear and cytosolic fractions. In vitro exposure of cell cytosolic fractions or highly purified 20S proteasome to low SAM:S-adenosylhomocysteine (SAH) ratios in the buffer also suppressed proteasome function, indicating that one or more methyltransferase(s) may be associated with proteasomal subunits. Immunoblotting a purified 20S rabbit red cell proteasome preparation using methyl lysine-specific antibodies revealed a 25 kDa proteasome subunit that showed positive reactivity with anti-methyl lysine. This reactivity was modified when 20S proteasome was exposed to differential SAM:SAH ratios. We conclude that impaired methylation of proteasome subunits suppressed proteasome activity in liver cells indicating an additional, yet novel mechanism of proteasome activity regulation by ethanol.

  20. U.S. Oxygenate Production

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

    By: Product Area May-15 Jun-15 Jul-15 Aug-15 Sep-15 Oct-15 View History Fuel Ethanol 29,666 29,684 30,256 29,621 28,543 30,139 1981-2015 Methyl Tertiary Butyl Ether (MTBE) 1,634...