Sample records for waiver mtbe methyl

  1. Atmospheric Methyl Tertiary Butyl Ether (MTBE) at a Rural Mountain Site in California

    E-Print Network [OSTI]

    Cohen, Ronald C.

    Atmospheric Methyl Tertiary Butyl Ether (MTBE) at a Rural Mountain Site in California Gunnar W. Schade,* Gabrielle B. Dreyfus, and Allen H. Goldstein ABSTRACT (CARB) measured MTBE in urban regions in 1995­ 1996, reporting a range of 0.4 to 13.2 ppbv in the LosMethyl tertiary butyl ether (MTBE

  2. Environmental Microbiology (2001) 3(6), 407416 Methyl tert-butyl ether (MTBE) degradation by a

    E-Print Network [OSTI]

    Environmental Microbiology (2001) 3(6), 407±416 Methyl tert-butyl ether (MTBE) degradation of California, Riverside, Riverside, CA 92521, USA. Summary The widespread use of methyl tert-butyl ether (MTBE is often proposed as the most promising alter- native after treatment. However, MTBE biodegradation appears

  3. Measurement of methyl-tert-butyl-ether (MTBE) in raw drinking water

    SciTech Connect (OSTI)

    Davisson, M L; Koester, C J; Moran, J E

    1999-10-14T23:59:59.000Z

    In order to assess the pathways for human exposure to methyl-tert-butyl-ether (MTBE) and to understand the extent of MTBE contamination in watersheds, a purge and trap gas chromatographic mass spectrometric method to measure part-per-trillion (ppt) concentrations of MTBE in environmental waters was developed. A variety of California's raw drinking waters were analyzed. No detectable MTBE was found in deep groundwater (>1000 feet). However shallow groundwater ({approx}250 feet) contained MTBE concentrations of non-detect to 1300 ppt. MTBE concentrations measured in rivers and lakes ranged from non-detect to 3500 ppt. East (San Francisco) Bay area rain water contained approximately 80 ppt MTBE.

  4. IDENTIFYING THE USAGE PATTERNS OF METHYL TERT-BUTYL ETHER (MTBE) AND OTHER OXYGENATES IN GASOLINE USING GASOLINE

    E-Print Network [OSTI]

    IDENTIFYING THE USAGE PATTERNS OF METHYL TERT-BUTYL ETHER (MTBE) AND OTHER OXYGENATES IN GASOLINE 1608 Mt. View Rapid City, SD 57702 Methyl tert-butyl ether (MTBE) is commonly added to gasoline. In 1998, 11.9 billion liters of MTBE were produced in the U.S. MTBE has been detected frequently

  5. Impacts of Ethanol on Anaerobic Production of Tert-Butyl Alcohol (TBA) from Methyl Tert-Butyl Ether (MTBE) in Groundwater

    E-Print Network [OSTI]

    Scow, K M; MacKay, Douglas

    2008-01-01T23:59:59.000Z

    Methyl Tert-Butyl Ether (MTBE) in Groundwater P.I. names,Methyl tert-butyl ether (MTBE) is a contaminant of concernsubsurface environments. MTBE appears to be degraded readily

  6. Photoionization of methyl t-butyl ether (MTBE) and t-octyl methyl ether (TOME) and analysis of their pyrolyses by

    E-Print Network [OSTI]

    Morton, Thomas Hellman

    Photoionization of methyl t-butyl ether (MTBE) and t-octyl methyl ether (TOME) and analysis 1999; accepted 20 July 1999 Abstract The pyrolysis products of neutral methyl-d3 t-butyl ether (MTBE-d3 from thermal cracking patterns. MTBE and TOME both exhibit base peaks at m/z 73 (which shifts to m/z 76

  7. Determination of methyl tert. butyl ether (MTBE) in gasoline

    SciTech Connect (OSTI)

    Feldman, J.; Orchin, M. (Univ. of Cincinnati, OH (United States))

    1993-02-01T23:59:59.000Z

    A GLC-acid extraction method is described for the determination of MTBE in gasolines. The method consists of a programmed GLC analysis starting at about room temperature conducted before and after extraction with cold 85% phosphoric acid. This treatment results in the preferential solubility of ethers and other oxygenated compounds while minimizing the reaction of olefins and aromatics which may be present in the gasolines. Plotting various known concentrations of MTBE in gasolines against the concentrations determined in the same samples by the authors methodology results in a straight line relationship. The concentration of MTBE in any sample of gasoline may thus be determined using their GLC-extraction procedure and the calibration line. The analysis can accommodate a wide choice of standard GLC columns and programs. 2 refs., 1 fig., 1 tab.

  8. RELATIONS BETWEEN THE DETECTION OF METHYL TERT-BUTYL ETHER (MTBE) IN SURFACE AND GROUND WATER AND ITS CONTENT IN GASOLINE

    E-Print Network [OSTI]

    RELATIONS BETWEEN THE DETECTION OF METHYL TERT-BUTYL ETHER (MTBE) IN SURFACE AND GROUND WATER.S. Geological Survey 1608 Mt. View Rapid City, SD 57702 Methyl tert-butyl ether (MTBE) is commonly used today, the one used most commonly is MTBE. To meet the oxygen requirements of the CAA Amendments, gasoline

  9. Acute toxicity of methyl-tertiary-butyl ether (MTBE) to aquatic organisms

    SciTech Connect (OSTI)

    BenKinney, M.T.; Barbieri, J.F.; Gross, J.S.; Naro, P.A. [Stonybrook Labs. Inc., Princeton, NJ (United States)

    1994-12-31T23:59:59.000Z

    Due to the recent amendment of the Clean Air Act, oxygenates are now being added to gasolines to boost octane and reduce air pollution from combustion in heavily populated areas. Oxygenates such as alcohols (i.e. methanol) and ethers (methyl-tertiary-butyl ether, MTBE) are commonly being used. A series of bioassay studies have been conducted with MTBE, one of the most commonly used octane-enhancing additives. Freshwater and marine studies were conducted with fish, invertebrates and algae to determine the impact of this material on the environment following accidental spills. Static-renewal studies were run to ensure maintenance of MTBE, a highly volatile material in the test containers. Chemical confirmation of exposure concentrations demonstrated the adequacy of the exposure system. Mysid shrimp were highly sensitive to MTBE, with significantly less effect observed with the other species evaluated. These data have implications for spill response, particularly since MTBE is slow to biodegrade and will rapidly move through groundwater. Comparative data for other oxygenates will also be discussed.

  10. Manipulation of the HIFVegf pathway rescues methyl tert-butyl ether (MTBE)-induced vascular lesions

    SciTech Connect (OSTI)

    Bonventre, Josephine A., E-mail: josephine.bonventre@oregonstate.edu [Rutgers, The State University of New Jersey, Joint Graduate Program in Toxicology, 170 Frelinghuysen Road, Piscataway, NJ 08854 (United States); Rutgers, The State University of New Jersey, Department of Biochemistry and Microbiology, 76 Lipman Dr., New Brunswick, NJ 08901 (United States); Oregon State University, Department of Environmental and Molecular Toxicology, 1011 Agricultural and Life Sciences Bldg, Corvallis, OR 97331 (United States); Kung, Tiffany S., E-mail: tiffany.kung@rutgers.edu [Rutgers, The State University of New Jersey, Joint Graduate Program in Toxicology, 170 Frelinghuysen Road, Piscataway, NJ 08854 (United States); Rutgers, The State University of New Jersey, Department of Biochemistry and Microbiology, 76 Lipman Dr., New Brunswick, NJ 08901 (United States); White, Lori A., E-mail: lawhite@aesop.rutgers.edu [Rutgers, The State University of New Jersey, Joint Graduate Program in Toxicology, 170 Frelinghuysen Road, Piscataway, NJ 08854 (United States); Rutgers, The State University of New Jersey, Department of Biochemistry and Microbiology, 76 Lipman Dr., New Brunswick, NJ 08901 (United States); Cooper, Keith R., E-mail: cooper@aesop.rutgers.edu [Rutgers, The State University of New Jersey, Joint Graduate Program in Toxicology, 170 Frelinghuysen Road, Piscataway, NJ 08854 (United States); Rutgers, The State University of New Jersey, Department of Biochemistry and Microbiology, 76 Lipman Dr., New Brunswick, NJ 08901 (United States)

    2013-12-15T23:59:59.000Z

    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 0.006255 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 HIFVegf 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 HippelLindau 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 HIFVegf 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.

  11. Alveolar breath sampling and analysis to assess exposures to methyl tertiary butyl ether (MTBE) during motor vehicle refueling

    SciTech Connect (OSTI)

    Lindstrom, A.B.; Pleil, J.D. [U.S. Environmental Protection Agency, Research Triangle Park, NC (United States)

    1996-07-01T23:59:59.000Z

    In this study we present a sampling and analytical methodology that can be used to assess consumers` exposures to methyl tertiary butyl ether (MTBE) that may result from routine vehicle refueling operations. The method is based on the collection of alveolar breath samples using evacuated one-liter stainless steel canisters and analysis using a gas chromatograph-mass spectrometer equipped with a patented `valveless` cryogenic preconcentrator. To demonstrate the utility of this approach, a series of breath samples was collected from two individuals (the person pumping the fuel and a nearby observer) immediately before and for 64 min after a vehicle was refueled with premium grade gasoline. Results demonstrate low levels of MTBE in both subjects` breaths before refueling, and levels that increased by a factor of 35 to 100 after the exposure. Breath elimination models fitted to the post exposure measurements indicate that the half-life of MTBE in the first physiological compartment was between 1.3 and 2.9 min. Analysis of the resulting models suggests that breath elimination of MTBE during the 64 min monitoring period was approximately 155 {mu}g for the refueling subject while it was only 30 {mu}g for the nearby observer. This analysis also shows that the post exposure breath elimination of other gasoline constituents was consistent with previously published observations. 20 refs., 3 figs., 4 tabs.

  12. Canada could get three MTBE plants

    SciTech Connect (OSTI)

    Anderson, E

    1990-03-01T23:59:59.000Z

    This article reports on the proposed development of three methyl tert-butyl ether (MTBE) plants in Canada. MTBE is used as an oxygenated fuel additive. The author discusses how demand for MTBE is increasing due to the regulation of leaded gasoline by the U.S. and Canadian governments. The exportation of MTBE from Canada to the U.S. is highlighted.

  13. Factors influencing biological treatment of MTBE contaminated ground water

    E-Print Network [OSTI]

    Stringfellow, William T.; Hines Jr., Robert D.; Cockrum, Dirk K.; Kilkenny, Scott T.

    2001-01-01T23:59:59.000Z

    Methyl tertiary-butyl ether (MTBE) biodegradation in batchCometabolic degradation of MTBE by a cyclohexane-oxidizingof 49 Biological Treatment of MTBE Fortin, N. Y. , and M. A.

  14. Biodegradation of methyl tertiary butyl ether (MTBE) using a granular activated carbon trickling filter

    SciTech Connect (OSTI)

    Converse, B.M.; Schroeder, E.D.; Chang, D.P.Y.

    1999-07-01T23:59:59.000Z

    A pilot scale trickling filter was constructed using granular activated carbon (GAC) as the packing medium and inoculated with a microbial culture known to degrade MTBE. The packing dimensions were 0.076 m in diameter and 0.22 m deep. The unit operated with recycling flow for two months before a biofilm was observed on the GAC. After two additional months the biofilm had visibly spread throughout the packing. A few pieces of GAC were placed in a sealed bottle with MTBE-contaminated water and nutrients. Headspace analysis performed over 14 days confirmed that MTBE degradation was occurring. The trickling filter was converted to continuous flow and operated for one month at a nominal flow rate of 0.1 L/min and a hydraulic loading rate of 32 m{sup 3}/m{sup 2}-d. Samples were collected for analysis at the spray nozzle and at the bottom of the trickling filter. Fractional removal varied with influent MTBE concentration, temperature and liquid flow rate. Percent MTBE removal was as high as 85%. A mechanical failure resulted in the trickling filter bed drying and percent removal dropping to less than 1 percent. However, the system recovered within five days.

  15. Oxidation of methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE) by ozone and combined ozone/hydrogen peroxide

    SciTech Connect (OSTI)

    Leitner, N.K.V.; Papailhou, A.L.; Croue, J.P.; Dore, M. (Univ. de Poitiers (France)); Peyrot, J. (British Petroleum, Harfleur (France))

    1994-01-01T23:59:59.000Z

    The aim of this work was to study the reaction of ozone and combined ozone/hydrogen peroxide on oxygenated additives such as methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE) in dilute aqueous solution using controlled experimental conditions. Experiments conducted in a semi-continuous reactor with MTBE and ETBE in combination (initial concentration: 2 mmol/L of each) showed that ETBE was better eliminated than MTBE with both ozone and combined O[sub 3]/H[sub 2]O[sub 2]. batch experiments led to the determination of the ratio of the kinetic constants for the reaction of OH[degree]-radical with MTBE and ETBE (k[sub OH[degree]/ETBE]/k[sub OH[degree]//MTBE] = 1.7). Tert-butyl formate and tert-butyl acetate were identified as the ozonation byproducts of MTBE an ETBE, respectively, while tert-butyl alcohol was found to be produced during the ozonation of both compounds. 10 refs., 10 figs., 1 tab.

  16. Methyl tert-butyl ether (MTBE) is a volatile organic com-pound (VOC) derived from natural gas that is added to gas-

    E-Print Network [OSTI]

    Methyl tert-butyl ether (MTBE) is a volatile organic com- pound (VOC) derived from natural gas Water in Urban and Agricultural Areas made from methanol, which is derived primarily from natural gas that is added to gas- oline either seasonally or year round in many parts of the United States to increase

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

    Reports and Publications (EIA)

    2001-01-01T23:59:59.000Z

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

  18. Evaluating nonmetallic materials` compatibility with MTBE and MTBE + gasoline service

    SciTech Connect (OSTI)

    Hotaling, A.C.

    1995-12-31T23:59:59.000Z

    Methyl-tertiary-butyl-ether (MTBE) has become the leading oxygenate in use in the petroleum industry. Since its introduction several years ago there has been premature deterioration of nonmetallic materials in both neat MTBE and MTBE + gasoline. This degradation is costly in several ways: maintenance, replacement, environmental, and product-loss. Identifying nonmetallic materials compatible with MTBE and MTBE + gasoline is important to the petroleum industry -- all the way from the refinery to the retail sale. Exposure tests have been conducted with different types of nonmetallics in neat MTBE, neat MTBE vapor, and 5% MTBE + 95% gasoline. As in previously reported tests, Teflon{reg_sign} laminates were the top performers, experiencing very little change in any of the properties tested. An ester and ether-based urethane laminate also exhibited only small property changes. Most materials displayed significant deterioration of one or more of the measured properties, even in MTBE condensing vapor and the 5% MTBE + 95% gasoline. The specific effects on each material need to be individually evaluated to determine the effect on service life.

  19. {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 [Department of Occupational and Environmental Health, School of Public Health and Military Preventive Medicine, Fourth Military Medical University, Xi'an 710032 (China); Zhang Yun [465 Hospital, Jilin Medical College, Jilin 132001 (China); Chen Yaoming; Liu Mingchao; Yao Ting; Yang Yanxia; Zhao Fang [Department of Occupational and Environmental Health, School of Public Health and Military Preventive Medicine, Fourth Military Medical University, Xi'an 710032 (China); Li Jingxia; Huang Chuanshu [Nelson Institute of Environmental Medicine, New York University School of Medicine, Tuxedo, New York 10987 (United States); Luo Wenjing [Department of Occupational and Environmental Health, School of Public Health and Military Preventive Medicine, Fourth Military Medical University, Xi'an 710032 (China)], E-mail: luowenj@fmmu.edu.cn; Chen Jingyuan [Department of Occupational and Environmental Health, School of Public Health and Military Preventive Medicine, Fourth Military Medical University, Xi'an 710032 (China)], E-mail: jy_chen@fmmu.edu.cn

    2009-04-15T23:59:59.000Z

    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.

  20. Drinking Water Problems: MTBE

    E-Print Network [OSTI]

    Dozier, Monty; Lesikar, Bruce J.

    2008-08-28T23:59:59.000Z

    Methyl tertiary-butyl ether, a gasoline additive commonly known as MTBE, can contaminate ground water and cause health problems for those exposed to it for a long time. However, filtering devices can remove this and other additives from well water...

  1. Review of potential technologies for the treatment of Methyl tertiary butyl Ether (MtBE) in drinking water

    SciTech Connect (OSTI)

    Brown, A.; Browne, T.E. [Komex H2O Science, Huntington Beach, CA (United States); Devinny, J.S. [Univ. of Southern California, Los Angeles, CA (United States)] [and others

    1997-12-31T23:59:59.000Z

    At present, the state of knowledge on effective treatment technologies for MtBE in drinking water, and groundwater in general, is limited. Research by others is focusing on the remediation of MtBE close to the point of release. The City of Santa Monica, MWD, Komex and USC are currently conducting research into different technologies that could be used to remove MtBE from drinking water supplies. The objectives of the research are to evaluate different treatment technologies to identify cost-effective and technically feasible alternatives for the removal of MtBE from drinking water. The evaluation is considering moderate to high water flow rates (100 to 2,000+ gpm) and low to moderate MtBE concentrations (<2,000 {mu}g/l). The research program includes four phases: (1) Literature Review; (2) Bench Scale Study; (3) Field Scale Pre-pilot Study; and (4) Summary Evaluation. This paper presents some preliminary information and findings from the first phase of this research - the literature review. The review discusses the chemical properties of MtBE and how they affect remediation and thus, an evaluation of alternative treatment technologies. The review of available literature, and the applicability and limitations of the following technologies are presented in detail.

  2. A review of treatment technologies for MTBE

    SciTech Connect (OSTI)

    Bass, D. [Groundwater Technology, Inc., Norwood, MA (United States)

    1995-12-31T23:59:59.000Z

    Available treatment technologies for methyl tertiary butyl ether (MTBE) contamination in soil, groundwater, and recovered groundwater are reviewed and assessed. MTBE contamination is becoming an important issue due to the increasing prevalence and regulation of this gasoline additive. In addition, MTBE is more soluble and more mobile in groundwater than most hydrocarbons, so it is usually the first gasoline constituent to reach sensitive receptors. Treatment of MTBE is complicated by its Henry`s constant, which is lower than most other gasoline constituents. Furthermore, evidence of biodegradability of MTBE is mixed, and MTBE does not degrade rapidly abiotically. Groundwater pumping is usually employed to contain and collect MTBE-contaminated groundwater, often successfully because of its high aqueous solubility. Air sparging/soil vapor extraction is also successfully employed to treat MTBE, but its effectiveness is reduced by the low Henry`s constant of MTBE. Sparging and other aerobic bioremediation approaches are hampered by the poor biodegradability of MTBE. Oxidation technologies, such as ozone injection, hold promise for rapid in situ remediation of MTBE. Treatment of recovered groundwater contaminated with MTBE is also problematic. MTBE adsorbs poorly to granular activated carbon; advanced oxidation processes are effective on MTBE, but entail high capital and operating costs; bioreactors are of questionable effectiveness on MTBE. Air stripping is usually the most cost-effective treatment technology for MTBE so long as the off gas from the air stripper can be discharged without treatment. However, off gas treatment is expensive, so groundwater is sometimes heated to reduce the requirement for stripping air.

  3. Economics of new MTBE design

    SciTech Connect (OSTI)

    Al-Jarallah, A.M.; Lee, A.K.K.

    1988-07-01T23:59:59.000Z

    Methyl Tertiary Butyl Ether (MTBE) is produced industrially by catalytic reaction between methanol and isobutene. The catalyst that is widely used is an acidic ion exchange resin. This article explores design and economics when sulfuric acid is the catalyst. The profitability of MTBE production depends mainly on the cost of butenes and methhanol. Thus, the example shows MTBE made with a catalyst of sulfuric acid was profitable at a Saudi Arabian location, even though it was not profitable at a U.S. Gulf Coast location.

  4. Methyl tertiary butyl ether (MtBE) contamination of the City of Santa Monica drinking water supply

    SciTech Connect (OSTI)

    Brown, A.; Farrow, J.R.C. [Komex H2O Science, Huntington Beach, CA (United States); Rodriguez, R.A. [City of Santa Monica, CA (United States)] [and others

    1997-12-31T23:59:59.000Z

    In the summer of 1996, the City of Santa Monica ceased pumping groundwater from two Well Fields (Charnock and Arcadia) used for public drinking water supply due to persistent and increasing concentrations of MtBE in all seven municipal water supply wells. This lost production accounted for 50% of the City`s total drinking water supply. In late 1996, the City, in cooperation with State and Federal agencies, initiated an investigation of MtBE contamination at the two well fields. The objectives of the investigation were as follows: (1) Review available data on the production, use, chemical characteristics, fate and transport, toxicology, and remediation of MtBE; (2) Identify locations of potential sources of MtBE groundwater contamination at the well fields; (3) Develop an understanding of the hydrologic pathways from the potential sources to the drinking water wells; and (4) Evaluate alternative treatment technologies for the removal of MtBE from drinking water. In addition to a review of available information about MtBE, the investigation included an extensive review of literature and available data relevant to the well fields, including well field production histories, site and regional hydrogeology, all well logs and production in the groundwater basins, general groundwater quality, and the record of MtBE detection. Based upon the review of background information, conceptual hydrogeologic models were developed. A detailed review of agency files for over 45 potential source sites was conducted. The information from this review was summarized, and source site screening and ranking criteria were developed. A field program was conducted at the major well field (Charnock), including soil gas surveys, CPTs, soil borings and well installations, geophysics, and aquifer testing. The field program provided site data which allowed the conceptual hydrogeologic model to be refitted to actual site conditions.

  5. Statoil outlines MTBE development program

    SciTech Connect (OSTI)

    Not Available

    1991-11-25T23:59:59.000Z

    This paper reports that Norway's state oil company Den Norkse state Oljeselskap AS has outlined plans to become one of the major European producers of methyl tertiary butyl ether in the 1990s. Statoil predicts European demand for MTBE will jump to 4.5 million metric tons/year by 2000 from 2.5 million tons in 1990. Europe currently is a net importer of MTBE, with a productive capacity of 2.2 million tons/year.

  6. Factors influencing biological treatment of MTBE contaminated ground water

    SciTech Connect (OSTI)

    Stringfellow, William T.; Hines Jr., Robert D.; Cockrum, Dirk K.; Kilkenny, Scott T.

    2001-09-14T23:59:59.000Z

    Methyl tert-butyl ether (MTBE) contamination has complicated the remediation of gasoline contaminated sites. Many sites are using biological processes for ground water treatment and would like to apply the same technology to MTBE. However, the efficiency and reliability of MTBE biological treatment is not well documented. The objective of this study was to examine the operational and environmental variables influencing MTBE biotreatment. A fluidized bed reactor was installed at a fuel transfer station and used to treat ground water contaminated with MTBE and gasoline hydrocarbons. A complete set of chemical and operational data was collected during this study and a statistical approach was used to determine what variables were influencing MTBE treatment efficiency. It was found that MTBE treatment was more sensitive to up-set than gasoline hydrocarbon treatment. Events, such as excess iron accumulation, inhibited MTBE treatment, but not hydrocarbon treatment. Multiple regression analysis identified biomass accumulation and temperature as the most important variables controlling the efficiency of MTBE treatment. The influent concentration and loading of hydrocarbons, but not MTBE, also impacted MTBE treatment efficiency. The results of this study suggest guidelines for improving MTBE treatment. Long cell retention times in the reactor are necessary for maintaining MTBE treatment. The onset of nitrification only occurs when long cell retention times have been reached and can be used as an indicator in fixed film reactors that conditions favorable to MTBE treatment exist. Conversely, if the reactor can not nitrify, it is unlikely to have stable MTBE treatment.

  7. Evaluation and Optimization of MTBE Biodegradation in Aquifers, Final Report

    SciTech Connect (OSTI)

    Legler, T; Balser, L; Koester, C; Wilson, W

    2004-02-13T23:59:59.000Z

    This study was focused on meeting the following objectives concerning the process of methyl tertiary butyl ether (MTBE) biodegradation, with the goal of optimizing this process in situ: 1. Assess whether intrinsic bioattenuation of MTBE is feasible under aerobic conditions across several contaminated sites. 2. Determine the effect of co-contaminants, specifically water-soluble gasoline components (most notably benzene, toluene, ethylbenzene and xylenes [BTEX]) on MTBE biodegradation. 3. Determine whether microbial and/or chemical factors contribute to different MTBE degradative activities. 4. Isolate and characterize MTBE-degrading microorganisms from sediments in which MTBE biodegradation was observed.

  8. UMass builds bugs to eat MTBE ByAuriaCimino

    E-Print Network [OSTI]

    Lovley, Derek

    UMass builds bugs to eat MTBE ByAuriaCimino STAfFWRITER An area university's process to destroy with methyl tertiary butyl ether (MTBE), which is found in gasoline. Once the first field trial is complete in particular has suffered from MTBE contamination because of the abundance of groundwater in the state, said

  9. Saudi MTBE project revived

    SciTech Connect (OSTI)

    NONE

    1996-01-17T23:59:59.000Z

    Alujain Corp., a member of the Xenel group of Saudi Arabia, is going ahead with plans to build an 800,000-m.t./year methyl tert-butyl ether (MTBE) plant. Bechtel has been appointed project manager for the plant, which will be owned by a new company, National Fuel Additives (Tahseen). Bechtel will help evaluate proposals already submitted for the lump sum turnkey job.

  10. MTBE, methanol prices rise

    SciTech Connect (OSTI)

    Morris, G.D.L.; Cornitius, T.

    1995-12-20T23:59:59.000Z

    After several months of drifting lower in line with declining autumn gasoline prices, tabs for methyl tert-butyl ether (MTBE) have turned around. There has been no big demand surge, but consumers and traders are beginning to build up inventories in advance of a series of midwinter shutdowns and turnarounds by producers. Spot prices, which dropped as low as 75 cts/gal, have rebounded to 90 cts/gal fob. Eager for a positive glimmer, methanol producers posted a 3-cts/gal increase in contract prices this month. It marks the first upward idea since February. In that time contract prices have dropped 75% from $1.55/gal to 39 cts/gal. A hard winter has hit early in much of the US sending natural gas prices up sharply. At the same time, formaldehyde and acetic acid markets remain firm, and with MTBE rebounding, methanol producers feel entitled to a piece of the action. {open_quotes}I don`t buy into this claim that MTBE demand is up and I don`t think producers can justify even a 3-cts/gal increase,{close_quotes} says one. {open_quotes}There is nothing in the economy to warrant a run-up. Housing starts are weaker, and demand is down at least 80,000 bbl/day with the MTBE shutdown.{close_quotes}

  11. MTBE -- A global perspective

    SciTech Connect (OSTI)

    Ludlow, W.I.; Miller, K.D. Jr.; Liew, R.E. van [DeWitt and Co., Inc., Houston, TX (United States)

    1995-09-01T23:59:59.000Z

    Methyl tertiary butyl ether (MTBE) is a major and familiar component of Reformulated and Oxygenated gasoline in the US. As such, it is essential to the success of the Clean Air Act programs now reaching a crescendo in major urban areas. In less than ten years, US MTBE capacity has grown from about 4,000 B/D to more than 200,000 B/D. Outside of the USA, its role is less widely understood. Although MTBE markets elsewhere are much less driven by legislation, they have seen the same spectacular growth prospects. Overall, about as much MTBE is used today overseas as in the US. To date, this has to be one of the petrochemical industry`s major success stories. Yet today, the MTBE industry stands at a crossroads, with the direction of future development uncertain at best. DeWitt`s gasoline and oxygenates team has closely observed the ups and downs of this market during most of its turbulent history. In this paper, the authors shall try to set down the major developments and prospects, with the personal familiarity of having been there when things changed. The story begins with a brief historical sketch, leading up to the identification of four critical periods in which major changes took place. The causes of today`s uncertainty lie in all of these stages, and are in a very real sense an example of the ``Law of Unintended consequences.`` Having set the stage, a cautious set of predictions will be put forth. These are neither as promising as proponents would like, nor as unpromising as some would tend to believe.

  12. Snamprogetti signs MTBE contracts

    SciTech Connect (OSTI)

    Alperowicz, N.

    1992-04-15T23:59:59.000Z

    Snamprogetti (Milan) will use a Russian-developed dehydrogenation process in a world-scale methyl tert-butyl ether (MTBE) plant it is to build at Arzew, Algeria for a previously announced joint venture of Sonatrach (Algiers), Total (Paris), and Ecofuel (Milan). The 600,000-m.t./year plant will be the first in the West to use the improved Snamprogetti-Yarsintez fluidized-bed dehydrogenation (FBD) technology proven on a demonstration plant at Yaroslavl, Russia. The process has also been selected for use in Oxyfuel Corp.`s 500,000-m.t./year MTBE plant near Beaumont, TX. Although the environmental permit is already in place, final agreement for this project has not yet been signed.

  13. Analysis of dissolved benzene plumes and methyl tertiary butyl ether (MTBE) plumes in ground water at leaking underground fuel tank (LUFT) sites

    SciTech Connect (OSTI)

    Happel, A.M.; Rice, D. [Lawrence Livermore National Lab., CA (United States); Beckenbach, E. [California Univ., Berkeley, CA (United States); Savalin, L.; Temko, H.; Rempel, R. [California State Water Resources Control Board, Sacramento, CA (United States); Dooher, B. [California Univ., Los Angeles, CA (United States)

    1996-11-01T23:59:59.000Z

    The 1990 Clean Air Act Amendments mandate the addition of oxygenates to gasoline products to abate air pollution. Currently, many areas of the country utilize oxygenated or reformulated fuel containing 15- percent and I I-percent MTBE by volume, respectively. This increased use of MTBE in gasoline products has resulted in accidental point source releases of MTBE containing gasoline products to ground water. Recent studies have shown MTBE to be frequently detected in samples of shallow ground water from urban areas throughout the United States (Squillace et al., 1995). Knowledge of the subsurface fate and transport of MTBE in ground water at leaking underground fuel tank (LUFT) sites and the spatial extent of MTBE plumes is needed to address these releases. The goal of this research is to utilize data from a large number of LUFT sites to gain insights into the fate, transport, and spatial extent of MTBE plumes. Specific goals include defining the spatial configuration of dissolved MTBE plumes, evaluating plume stability or degradation over time, evaluating the impact of point source releases of MTBE to ground water, and attempting to identify the controlling factors influencing the magnitude and extent of the MTBE plumes. We are examining the relationships between dissolved TPH, BTEX, and MTBE plumes at LUFT sites using parallel approaches of best professional judgment and a computer-aided plume model fitting procedure to determine plume parameters. Here we present our initial results comparing dissolved benzene and MTBE plumes lengths, the statistical significance of these results, and configuration of benzene and MTBE plumes at individual LUFT sites.

  14. EPA proposal sets MTBE back

    SciTech Connect (OSTI)

    Lucas, A.

    1995-01-04T23:59:59.000Z

    Methyl tert-butyl ether (MTBE) producers were looking for a boost from the official New Year`s start of EPA`s reformulated gasoline (RFG) program. But that prospect has been dimmed by an EPA-proposal-in reaction to concerns about RFG prices-to allow states to withdraw from the program. The states that have opted to out make up 5%-6% of the total RFG pool says Arthur Zadronzy, director/government outreach for MTBE producer Arco Chemical. {open_quotes}This is not a major hit, but it is one we have felt,{close_quotes} he says. Despite the state and EPA actions, MTBE producers are not worried about long-term consequences.

  15. Impacts of Ethanol on Anaerobic Production of Tert-Butyl Alcohol (TBA) from Methyl Tert-Butyl Ether (MTBE) in Groundwater

    E-Print Network [OSTI]

    Scow, K M; MacKay, Douglas

    2008-01-01T23:59:59.000Z

    Project title: Impacts of Ethanol on Anaerobic Production oftert-butanol (TBA). As ethanol is being promoted as ainvestigate the effect of ethanol release on existing MTBE

  16. Petrochem industry expands North American MTBE capacity

    SciTech Connect (OSTI)

    Not Available

    1992-10-05T23:59:59.000Z

    This paper reports that petrochemical manufacturers continue to increase methyl tertiary butyl ether (MTBE) capacity in North America. The action reflects refiners' reformulation of gasoline to help reduce auto emissions. Demand for gasoline blending oxygenates such as MTBE is expected to increase as U.S. refiners reconfigure processing trains to produce fuels meeting requirements of the Clean Air Act amendments of 1990. Recent progress includes plans to build an MTBE plant in Mexico and start-ups of plants on the U.S. Gulf Coast and in Canada.

  17. MTBE: Wild card in groundwater cleanup

    SciTech Connect (OSTI)

    Koenigsberg, S. [Regenesis Bioremediation Products, San Juan Capistrano, CA (United States)

    1997-11-01T23:59:59.000Z

    Subsurface releases of the gasoline oxygenate, methyl tertiary butyl ether (MTBE) seriously compromise the remediation and closure of properties that have ground water contaminated with BTEX and other conventional fuel hydrocarbon components. Although a manageable protocal for BTEX remediation is being set up, the MTBE problem continues to be difficult. This article discusses a new magnesium peroxide compound which could be part of the solution. Covered topics include oxygen release compound (ORC) enhance bioremediation and the role of oxygen and ORC in MTBE remediation. 1 fig.

  18. MTBE from butadiene-rich C/sub 4/s

    SciTech Connect (OSTI)

    Ancillotti, F.; Pescarollo, E.; Szatmari, E.; Lazar, L.

    1987-12-01T23:59:59.000Z

    Methyl tert-butyl ether (MTBE), is made by reacting methanol with isobutylene. The preferred source of isobutylene is a steam cracker C/sub 4/ cut from which butadiene has been removed. However, moving the MTBE synthesis upstream of the butadiene extraction will improve the extraction step. The following is a review of conditions imposed on the MTBE unit's design and operation when placed in this new location.

  19. MTBE still in poor health, despite the Clean Air Act

    SciTech Connect (OSTI)

    Wood, A.

    1994-05-25T23:59:59.000Z

    After the second winter oxygenated fuels program of the 1990 Clean Air Act, producers of methyl tert-butyl ether (MTBE) are still feeling the chill of poor profitability. Despite the strong demand growth for MTBE to meet oxygen requirements in reformulated gasoline (RFG), oversupply still dogs the market. That, combined with a run-up in feedstock prices, has seen margins for MTBE markers all but evaporate. And it seems matters are likely to get worse before they get better. This week, Belvieu Environmental Fuels (BEF; Houston) expects to startup its 15,000-bbl/day MTBE plant at Mont Belvieu, TX. In late July, Texaco will start up its 15,000-bbl/day MTBE/propylene oxide (PO) plant at Port Neches, TX. In addition, a rash of refinery-based MTBE and tert-amyl methyl ether projects are nearing completion. {open_quotes}Profitability in MTBE has been extremely poor,{close_quotes} says Marvin O. Schlanger, president of Arco Chemical Americas, the largest MTBE producer. There has, however, been some recent recovery on the spot market, with MTBE moving from less than 60 cts/gal to near cash-cost levels of 70 cts/gal. But contract prices remain depressed, and strength in butane and methanol pricing have all buy wiped out any gains in MTBE.

  20. Author's personal copy Automobile proximity and indoor residential concentrations of BTEX and MTBE

    E-Print Network [OSTI]

    Siegel, Jeffrey

    Author's personal copy Automobile proximity and indoor residential concentrations of BTEX and MTBE to indoor benzene and MTBE concentrations appeared to have been dominated by car exhaust concentrations of other BTEX components and methyl tert-butyl ether (MTBE) have been reported [5,6]. Up until

  1. Biotreatment of groundwater contaminated with MTBE: interaction of common environmental co-contaminants

    E-Print Network [OSTI]

    Biotreatment of groundwater contaminated with MTBE: interaction of common environmental co November 2005 Key words: aerobic, biodegradation, BTEX, co-contaminant, MTBE, TBA Abstract Contamination of groundwater with the gasoline additive methyl tert-butyl ether (MTBE) is often accompanied by many aromatic

  2. MTBE still facing pressure from ethanol under latest fuel proposal

    SciTech Connect (OSTI)

    Lucas, A.

    1994-01-26T23:59:59.000Z

    The US EPA's finalized reformulated gasoline rule, part of Phase II of the 1990 Clean Air Act, signals a possible turnaround for the sluggish methyl tert-butyl ether (MTBE) market. But if a 30% renewable fuels proposal favoring ethanol passes, pressure could continue for MTBE.

  3. MTBE: The headache of cleaner air

    SciTech Connect (OSTI)

    Kneiss, J.

    1995-07-01T23:59:59.000Z

    Gasoline with methyl tertiary butyl ether (MTBE) has been sold in the United States since 1979, when it was added to fuels as an octane enhancer after lead was phased out of motor fuels. Recently it has been introduced as a means of reducing carbon monoxide emissions during the winter months in targeted US cities. However, there is concern over health complaints including headaches, dizziness and nausea from residents of some areas. These reports have launched an era of assidious research by scientists and public health officials across the country to learn more about MTBE`s short-term and long-term, and possibly carcinogenic, health effects. New research should help weigh the risk of MTBE as a possible carcinogen and the effectiveness of MTBE-blended fuels in reducing carbon monoxide levels. The question is whether, in minimizing one risk, is another risk - however small - being introduced?

  4. MTBE: Capacity boosts on hold amid demand concerns

    SciTech Connect (OSTI)

    NONE

    1995-05-03T23:59:59.000Z

    Uncertainty reigns in the methyl tert-butyl ether (MTBE) market. {open_quotes}We have no choice but to put our expansion plans on the back burner,{close_quotes} says one producer. {open_quotes}Because of government actions, there are no MTBE plants being built or expanded.{close_quotes} Spot MTBE prices have risen ti 82 cts- 83 cts/gal from 76 cts-78 cts/gal earlier this month as the demand for octane enhancement increases for the summer driving season. Some observers say EPA may relax different oxygen requirements for gasoline in different seasons. That would simplify production and supply for MTBE makers.

  5. Global developments in MTBE

    SciTech Connect (OSTI)

    Feller, L.W. [CMAI, Houston, TX (United States)

    1995-12-31T23:59:59.000Z

    This paper is intended to provide an overview of some of the recent developments in MTBE demand growth worldwide and the impact of these developments on MTBE demand in the future. It provides a perspective of the influence of developments in the US on the worldwide MTBE markets. The public`s outcry regarding oxygenates in gasoline, and specifically MTBE, that has been evolving in the US during the past several months is in response to a politically mandated requirement for a fuel that contains oxygen that is provided by MTBE or ethanol. This public unrest had negatively impacted the market price for MTBE at the time this paper was being prepared. However, the author believes that MTBE, because of its clean octane capabilities, will continue to be used as an octane blendstock for gasoline in increasing quantities worldwide as we move through lead phasedown in West Europe and other countries that are experiencing pollution problems relating to exhaust emissions from internal combustion engines. The objectives of this paper are as follows: review developments in MTBE demand 1990--2000; identify regions where MTBE demand growth will occur; review production growth for MTBE, both historical and forecast; examine world trade patterns during the period; assess methanol demand growth during the period; analyze MTBE`s regional price bias; and provide a forecast of future MTBE price trends.

  6. Falling MTBE demand bursts the methanol bubble

    SciTech Connect (OSTI)

    Wiesmann, G.; Cornitius, T.

    1995-03-01T23:59:59.000Z

    Methanol spot markets in Europe and the US have been hit hard by weakening demand from methyl tert-butyl ether (MTBE) producers. In Europe, spot prices for domestic T2 product have dropped to DM620-DM630/m.t. fob from early-January prices above DM800/m.t. and US spot prices have slipped to $1.05/gal fob from $1.35/gal. While chemical applications for methanol show sustained demand, sharp methanol hikes during 1994 have priced MTBE out of the gasoline-additive market. {open_quotes}We`ve learned an important lesson. We killed [MTBE] applications in the rest of the world,{close_quotes} says one European methanol producer. Even with methanol currently at DM620/m.t., another manufacturer points out, MTBE production costs still total $300/m.t., $30/m.t. more than MTBE spot prices. Since late 1994, Europe`s 3.3-million m.t./year MTBE production has been cut back 30%.

  7. Add MTBE unit ahead of alkylation

    SciTech Connect (OSTI)

    Masters, K.R.; Prohaska, E.A.

    1988-08-01T23:59:59.000Z

    Approximately three years ago, the people at Diamond Shamrock's Sunray, Texas, refinery recognized a growing demand for high octane super premium unleaded gasoline in their regional marketing area. It was apparent that they would need to change their processing scheme to meet this growing demand. After investigating several options, they decided to install an MTBE (methyl tert-butyl ether) unit upstream of their existing sulfuric acid (H/sub 2/SO/sub 4/) aklylation unit. The new unit would process olefin feed before it entered the alkylation unit. The MTBE unit was expected to improve Diamond Shamrock's gasoline pool in two ways. First, the MTBE would be an additional high octane blending stock for the gasoline pool. Second, the MTBE unit would improve the quality of the olefin stream going to the alkylation unit. Diamond Shamrock brought their MTBE unit onstream in December, 1985. The results of the combined operation exceeded expectations, producing alkylate in excess of 98 RON (Research octane number) and MTBE of 118 RON. These components significantly upgraded the refinery's capability to produce a super premium unleaded gasoline.

  8. The MTBE solution: Octanes, technology, and refinery profitability

    SciTech Connect (OSTI)

    Lander, E.P.; Hubbard, J.N.; Smith, L.A.

    1983-03-01T23:59:59.000Z

    This paper has been developed to provide refiners with business decision insight regarding the production of methyl tertiary butyl ether (MTBE) from refinery - (FCC) produced isobutylene. The driving forces making MTBE an attractive investment are examined with regard to the increasing demand for higher octane unleaded gasolines. The decision to proceed with MTBE production depends on the profitability of such an investment and the refiner's ability to meet market demands using available processing equipment, refinery produced streams and external feedstocks. The factors affecting this decision are analyzed in this paper and include: industry ability to meet rising octane demand; profit potential realized by diverting isobutylene to MTBE; availability of technology for producing MTBE; and investment and operating costs required to produce MTBE. Chemical Research and Licensing and NEOCHEM have developed a simple, low cost process to produce MTBE, reducing the excessive equipment and high operating costs that were associated with conventional MTBE designs. The economics and process benefits of installing a CRandL/NEOCHEM MTBE process are examined within the framework of a generalized medium-sized refinery configuration.

  9. Motor Gasoline Outlook and State MTBE Bans

    Reports and Publications (EIA)

    2003-01-01T23:59:59.000Z

    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.

  10. Experimental Pathology Laboratories, Inc. Methyl-Tertiary-Butyl Ether

    E-Print Network [OSTI]

    Baker, Chris I.

    COORDINATOR'S REPORT FOR LIFETIME CARCINOGENICITY STUDY OF METHYL-TERTIARY-BUTYL ETHER (MTBE) IN SPRAGUE CARCINOGENICITY STUDY OF METHYL-TERTIARY-BUTYL ETHER (MTBE) IN SPRAGUE-DAWLEY RATS CONDUCTED AT THE CANCER

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

    Reports and Publications (EIA)

    1999-01-01T23:59:59.000Z

    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.

  12. Veba in MTBE project, cutting aromatics

    SciTech Connect (OSTI)

    Young, I.; Roberts, M.

    1992-04-15T23:59:59.000Z

    The new owners of the refinery and petrochemical complex at Schwedt in eastern Germany-RWE-DEA (Hamburg), Veba Oel (Gelsenkirchen), Agip (Rome), Total (Paris), and Elf-Aquitaine (Paris)-plan to build a 60,000-m.t./year methyl tert-butyl ether (MTBE) plant at the site for 1994-1995 completion. The MTBE project forms part of the consortium`s announced DM1.5-billion ($500 million) investment program for the complex that aims to raise refinery throughput from 8 million m.t./year to 12 million m.t./year by 1994 and hike production of naphtha and benzene.

  13. Methanex considers methanol, MTBE in Qatar

    SciTech Connect (OSTI)

    NONE

    1995-12-13T23:59:59.000Z

    CW has learned that Methanex Corp. is considering entering one of two methanol and methyl tert-butyl ether (MTBE) projects in Qatar. Executive v.p. Michael Wilson says that part of the company`s New Zealand plant could be moved to a site in Qatar, which would lower capital costs for the possible project by $75 million-$100 million. Both Qatar General Petroleum Corp. and Qatar Fuel Additives are developing methanol and MTBE projects at Umm Said, Qatar. Methanex says its goal is to ensure low-cost feedstocks.

  14. Total to withdraw from Qatar methanol - MTBE?

    SciTech Connect (OSTI)

    NONE

    1996-05-01T23:59:59.000Z

    Total is rumored to be withdrawing from the $700-million methanol and methyl tert-butyl ether (MTBE) Qatar Fuel Additives Co., (Qafac) project. The French company has a 12.5% stake in the project. Similar equity is held by three other foreign investors: Canada`s International Octane, Taiwan`s Chinese Petroleum Corp., and Lee Change Yung Chemical Industrial Corp. Total is said to want Qafac to concentrate on methanol only. The project involves plant unit sizes of 610,000 m.t./year of MTBE and 825,000 m.t./year of methanol. Total declines to comment.

  15. Ecological hazards of MTBE exposure: A research agenda

    SciTech Connect (OSTI)

    Carlsen, T.; Hall, L.; Rice, D.

    1997-03-01T23:59:59.000Z

    Fuel oxygenates are used in metropolitan areas across the United States in order to reduce the amount of carbon monoxide released into the atmosphere during the winter. The most commonly used fuel oxygenate is Methyl tert-butyl ether (MTBE). Its widespread use has resulted in releases into the environment. To date there has been only minimal effort to investigate ecological impacts caused by exposure to concentrations of MTBE typically found in environmental media. Research into the potential for MTBE to adversely affect ecological receptors is essential. Acquisition of such baselines data is especially critical in light of continuing inputs and potential accumulation of MTBE in environmental media. A research Agenda is included in this report and addresses: Assessing Ecological Impacts, Potential Ecological Impacts of MTBE (aquatic organisms, terrestrial organisms), Potential Ecological Endpoints, and A Summary of Research Needs.

  16. Korean oxygenates rule sparks MTBE capacity plans

    SciTech Connect (OSTI)

    Kim, Hyung-Jin

    1994-06-15T23:59:59.000Z

    The Korean government`s strict standard for gasoline sold domestically is expected to have a significant impact on the methyl tert-butyl ether (MTBE) market. The mandate-requiring gasoline oxygen content of 0.5% this year, 0.75% by 1996, and 1.0% by 1998-has sparked a rush by Korean refineries to build new MTBE plants. If expansion plans are carried out, Korea`s MTBE capacity will increase from 280,000 m.t./year to 650,000 m.t./year by 1996, far surpassing predicted demand. Honam Oil, part of the Lucky Group, plans startup of a 100,000-m.t./year unit at Yeochon by early 1996. In addition, by the end of 1996 Ssangyong Oil will bring a 100,000-m.t./year unit onstream.

  17. Ecofuel plans MTBE plant in Italy

    SciTech Connect (OSTI)

    Alperowicz, N.

    1992-04-29T23:59:59.000Z

    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.

  18. Health studies indicate MTBE is safe gasoline additive

    SciTech Connect (OSTI)

    Anderson, E.V.

    1993-09-01T23:59:59.000Z

    Implementation of the oxygenated fuels program by EPA in 39 metropolitan areas, including Fairbanks and Anchorage, Alaska, in the winter of 1992, encountered some unexpected difficulties. Complaints of headaches, dizziness, nausea, and irritated eyes started in Fairbanks, jumped to Anchorage, and popped up in various locations in the lower 48 states. The suspected culprit behind these complaints was the main additive for oxygenation of gasoline is methyl tert-butyl ether (MTBE). A test program, hastily organized in response to these complaints, has indicated that MTBE is a safe gasoline additive. However, official certification of the safety of MTBE is still awaited.

  19. MTBE growth limited despite lead phasedown in gasoline

    SciTech Connect (OSTI)

    Storck, W.

    1985-07-15T23:59:59.000Z

    This month's legislated reduction of the allowable amount of lead additives in gasoline will increase demand strongly for methyl-tert-butyl ether (MTBE) as an octane enhancer, but the economics of the refinery business and the likelihood of rapidly increasing high-octane gasoline imports probably will limit the size of the business in coming years. MTBE will be used to fill the octane gap now, but economics and imports of gasoline later on could hold down demand. The limited growth in sales of MTBE is discussed.

  20. MTBE, ethanol rules come under fire

    SciTech Connect (OSTI)

    Begley, R.

    1995-03-01T23:59:59.000Z

    EPA is facing stiff challenges to the mandates for methyl tert-butyl ether (MTBE) and ethanol in its reformulated gasoline (RFG) program. Wisconsin officials are receiving hundreds of complaints about the alleged health effects and other problems with MTBE added to gasoline, and Gov. Tommy Thompson is demanding that EPA suspend the RFG program until April 1. Rep. James Sensenbrenner (R., WI) is threatening to introduce a bill to repeal the program in Wisconsin if EPA does not comply. However, EPA administrator Carol Browner says the agency will {open_quotes}defer any decision{close_quotes} on the request. EPA has sent technical experts to Milwaukee to respond to and monitor citizens` complaints.

  1. Modeling the atmospheric inputs of MTBE to groundwater systems

    SciTech Connect (OSTI)

    Pankow, J.F.; Johnson, R.L. [Oregon Graduate Inst., Portland, OR (United States). Dept. of Environmental Science and Engineering; Thomson, N.R. [Univ. of Waterloo, Ontario (Canada). Dept. of Civil Engineering

    1995-12-31T23:59:59.000Z

    A numerical transport model was used to calculate the movement of methyl-t-butyl ether (MTBE) and several other volatile organic compounds (VOCs) from the atmosphere downward through the unsaturated zone and into shallow groundwater. Simulations were carried out for periods as long as 10 years to investigate whether a gaseous atmospheric MTBE source at typical ambient concentrations could account for the presence of MTBE in shallow groundwater at the types of low ug/L levels that have been found during the National Water Quality Assessment Program currently being conducted by the US Geological Survey. The simulations indicate that downward movement of MTBE to shallow groundwater will be very slow when there is no net downward movement of water through the vadose zone. For example, for a vadose zone composed of fine sand, and assuming tens of cm of infiltration, then only a few years will be required for water at a water table that is 5.0 m below ground surface to attain MTBE levels that correspond to saturation with respect to the atmospheric source gaseous concentration. An on/off atmospheric source, as might occur in the seasonal use of MTBE, will lead to concentrations in shallow groundwater that correspond to saturation with the time-averaging atmospheric source concentration.

  2. anhydride-vinyl methyl ether: Topics by E-print Network

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

    TREAT METHYL- TERT-BUTYL ETHER CONTAMINATED CiteSeer Summary: Methyl-tert-butyl ether (MTBE) is a commonly used gasoline additive. Leaking underground storage tank systems,...

  3. Remediation of MTBE in groundwater: A case where pump-and-treat works

    SciTech Connect (OSTI)

    Bass, D.H.; Riley, B. [Groundwater Technology, Inc., Norwood, MA (United States); Farrell, T. [Groundwater Technology, Inc., Trenton, NJ (United States)

    1994-12-31T23:59:59.000Z

    Two case studies are discussed in which groundwater pumping reduced levels of dissolved methyl tertiary butyl ether (MTBE) in groundwater by more than two orders of magnitude, in some cases to below detection limits. MTBE contamination in groundwater is becoming an important issue due to the increasing prevalence and regulation of this gasoline additive. In addition, MTBE is more mobile in groundwater than most hydrocarbons, so it is usually the first gasoline constituent to reach sensitive receptors. Since its Henry`s constant is low, in situ removal of MTBE from groundwater by air sparging is slow, and MTBE does not rapidly degrade, either biologically or abiotically. Therefore, groundwater pumping is usually employed to contain and collect MTBE-contaminated groundwater. Pumping groundwater can reduce MME levels to below detection limits within a few years, because MTBE in the subsurface is found mostly dissolved in groundwater. In contrast, the more hydrophobic gasoline hydrocarbons exist mostly in pockets of separate phase material and adsorbed to soil particles and dissolve slowly in groundwater. Hydrocarbon concentrations are rarely reduced to closure levels within a reasonable time frame by pumping. Sites in eastern Massachusetts and southern New Jersey, where groundwater was contaminated with MTBE due to releases of unleaded gasoline from underground storage tanks, are discussed. At these sites, average MTBE levels were reduced by two to three orders of magnitude, from several ppm or more to less than 10 ppb within three years by pumping groundwater at 10 to 30 gpm.

  4. Accurate Computer Simulation of Phase Equilibrium for Complex Fluid Mixtures. Application to Binaries Involving Isobutene, Methanol, Methyl tert-Butyl Ether, and

    E-Print Network [OSTI]

    Lisal, Martin

    to Binaries Involving Isobutene, Methanol, Methyl tert-Butyl Ether, and n-Butane Martin Lisal,*,, William R + methyl tert-butyl ether (MTBE) and the binaries formed by methanol with isobutene, MTBE, and n

  5. Meeting the challenge of MTBE biodegradation

    SciTech Connect (OSTI)

    Eweis, J.B.; Chang, D.P.Y.; Schroeder, E.D.; Scow, K.M. [Univ. of California, Davis, CA (United States); Morton, R.L.; Caballero, R.C. [Los Angeles County Sanitation Districts, Carson, CA (United States). Joint Water Pollution Control Plant

    1997-12-31T23:59:59.000Z

    Oxygenated and reformulated gasolines have been developed in response to air pollution control regulations targeted at reducing carbon monoxide emissions and photochemical air pollution. The 1990 Clean Air Act Amendments required the addition of fuel oxygenates to gasoline in areas where the level of carbon monoxide exceeded national ambient air quality standards. In the South Coast Air Basin gasoline containing oxygenated compounds has been in use since the late 1980`s. One oxygenated fuel additive most often selected by producers to meet the requirements is methyl tert-butyl ether (MTBE). However, large production numbers associated with MTBE production, combined with the compound`s high water solubility, chemical stability, and toxicity, make it a potentially important groundwater pollutant. The County Sanitation District of Los Angeles, Joint Water Pollution Control Plant in Carson, California is one of the few wastewater treatment plants in the nation that receives refinery wastewater discharge. It has operated several pilot-scale compost-based biofilters for control of various volatile organic contaminants throughout the plant since a 1991 joint study with the University of California, Davis. After one year of operation, one of the biofilters spontaneously developed the ability to degrade MTBE. The paper describes the collaborative efforts to determine the feasibility of transferring the degrading microbial population from the solid to liquid phase, without loss of activity, and to determine some of the environmental requirements necessary for survival of the microbial culture.

  6. Treatment of Methyl tert-Butyl Ether Vapors in Biotrickling Filters. 2.

    E-Print Network [OSTI]

    vapors of methyl tert-butyl ether (MTBE), a gasoline additive of great environmental concern MTBE treatment are discussed. Introduction The rapidly rising number of reports of groundwater con- taminated with the gasoline additive methyl tert-butyl ether (MTBE) has raised concerns about its

  7. Race to license new MTBE and TAME routes heats up

    SciTech Connect (OSTI)

    Rotman, D.

    1993-01-06T23:59:59.000Z

    With refineries and petrochemical manufacturers continuing to gear up production of oxygenates for use in reformulated fuels, new routes to methyl tert-butyl ether (MTBE) and tert-amyl methyl ether (TAME) are clearly hot items in the licensing market. And probably nowhere has the competition become as intense as in offerings for skeletal isomerization technologies to boost ethers production from fluid catalytic cracking and steam cracking.

  8. Health risks associated with exposure to gasoline additives-methyl tertiary butyl ether [MTBE]. Hearing before a Subcommittee of the Committee on Appropriations, United States Senate, One Hundred Third Congress, First Session, Special Hearing

    SciTech Connect (OSTI)

    Not Available

    1993-01-01T23:59:59.000Z

    This hearing focuses on an Alaskan study by the Centers for Disease Control which examines possible health risks associated with exposure to gasoline additive know as MTBE. Testimony is given by Dr. William Roper, Director, CDC.

  9. US refiners choose variety of routes to MTBE

    SciTech Connect (OSTI)

    Rhodes, A.K.

    1992-09-07T23:59:59.000Z

    This paper reports that refiners and merchant manufacturers in the U.S. are gearing up to produce the large volumes of methyl tertiary butyl ether (MTBE) needed to comply with oxygenated gasoline requirements. The 1990 U.S. Clean Air Act Amendments specify that, as of the first of this coming November, gasoline containing a minimum of 2.7 wt % oxygen must be sold in 39 CO-nonattainment cities. Refiners and others are scurrying to bring MTBE capacity on line in time to meet this requirement. Many U.S. refiners already have some operating MTBE capacity, but this will not be nearly enough to meet the looming increase in demand. As a result, additional capacity is being constructed worldwide.

  10. Effect of lower feedstock prices on economics of MTBE complex

    SciTech Connect (OSTI)

    Rahman, F.; Hamid, S.H.; Ali, M.A. [King Fahd Univ. of Petroleum and Minerals, Dhahran (Saudi Arabia)

    1996-01-01T23:59:59.000Z

    Economic evaluation of the methyl tertiary butyl ether (MTBE) complex was carried out starting from n-butane and by captive production of methanol from natural gas. The processing steps consist of isomerization of n-butane to isobutane, dehydrogenation of isobutane to make isobutene, and finally, the reaction of isobutene with methanol to produce MTBE. Two different plant sizes were considered, and the effect of 30% lower feedback prices on profitability was studied. It was found that the raw materials cost is a dominant component, composing about 55% of the total production cost. An internal rate of return of 19% could be realized for 500,000 tons per annum MTBE complex based on economic data in mid-1993. The payback period estimated at this capacity was 3.8 years, and the break-even capacity was 36.6%.

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

    Reports and Publications (EIA)

    2006-01-01T23:59:59.000Z

    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.

  12. A near infrared regression model for octane measurements in gasolines which contain MTBE

    SciTech Connect (OSTI)

    Maggard, S.M. (Ashland Petroleum Co., KY (USA))

    1990-01-01T23:59:59.000Z

    Near infrared (NIR) spectroscopy has emerged as a superior technique for the on-line determination of octane during the blending of gasoline. This results from the numerous advantages that NIR spectroscopy has over conventional on-line instrumentation. Methyl t-butyl ether (MTBE) is currently the oxygenated blending component of choice. MTBE is advantageous because it has a high blending octane, a low Reid vapor pressure, is relatively cheap, and does not form peroxides (1). The goal of this project was to develop a NIR regression model that could be used to predict pump octanes regardless of whether they contained MTBE.

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

    SciTech Connect (OSTI)

    Wolfe, R.

    1995-12-31T23:59:59.000Z

    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.

  14. MTBE Production Economics

    Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645 3,625 1,006 492 742 33 111 1,613 122 40 Buildingto17 3400, U.S.MajorMarketsNov-14Biomass feedstocks and0216,JulyMTBE

  15. Detections of MTBE in surficial and bedrock aquifers in New England

    SciTech Connect (OSTI)

    Grady, S.J. [Geological Survey, Hartford, CT (United States)

    1995-12-31T23:59:59.000Z

    The gasoline additive methyl tert-butyl ether (MTBE) was detected in 24% of water samples collected from surficial and bedrock aquifers in areas of New England. MTBE was the most frequently detected volatile organic compound among the 60 volatile chemicals analyzed and was present in 33 of 133 wells sampled from July 1993 through September 1995. The median MTBE concentration measured in ground-water samples was 0.45 microgram per liter and concentrations ranged from 0.2 to 5.8 microgram per liter. The network of wells sampled for MTBE consisted of 103 monitoring wells screened in surficial sand-and-gravel aquifers and 30 domestic-supply wells in fractured crystalline bedrock aquifers. Seventy-seven percent of all MTBE detections were from 26 shallow monitoring wells screened in surficial aquifers. MTBE was detected in42% of monitoring wells in urban areas. In agricultural areas, MTBE was detected i 8% (2 of 24) of wells and was not detected in undeveloped areas. Sixty-two percent of the MTBE detections in surficial aquifers were from wells within 0.25 mile of gasoline stations or underground gasoline storage tanks; all but one of these wells were in Connecticut and Massachusetts, where reformulated gasoline is used. MTBE was detected in 23% of deep domestic-supply wells that tapped fractured bedrock aquifers. MTBE was detected in bedrock wells only in Connecticut and Massachusetts; land use near the wells was suburban to rural, and none of the sampled bedrock wells were within 0.25 mile of a gasoline station.

  16. Remediation of overlapping benzene/MTBE and MTBE-only plumes: A case study

    SciTech Connect (OSTI)

    Carpenter, P.L. [TolTest, Inc., Pittsburgh, PA (United States); Vinch, C.A. [Ryder Transportation Services, Lawrenceville, NJ (United States)

    1997-12-31T23:59:59.000Z

    Two overlapping dissolved hydrocarbon plumes were identified in the shallow water-bearing zone at a commercial vehicle service and fueling facility. Plume 1 originated from a pre-1993 gasoline product line/dispenser leak. This plume contained a relatively common mix of benzene, toluene, ethylbenzene, xylenes (BTEX), and methyl tert-butyl ether (MTBE); benzene and MTBE were identified as the Plume 1 contaminants of concern based on their detection at approximately 200 {mu}g/l each, which exceeded regulatory guidance. Plume 2, which was detected in the tank cavity during UST removal, resulted from gasoline line leaks/underground storage tank overfills. Although the majority of impacted soils in both the dispenser and tank cavity areas were removed during UST excavation, rainfall during impacted soil removal mobilized the MTBE contained in the soils to groundwater. As a result, Plume 2 contained approximately 900 {mu}g/l MTBE while BTEX compounds were non-detect. Although the impacted zone sustained an approximate yield of only 0.3 gallon per minute, Pennsylvania regulations dictate that this zone must be treated as an aquifer. The failure of remediating gasoline plumes using pump-and-treat has been predominantly due to BTEX`s tendency to adsorb onto soil, creating a residual-phase product layer which acts as a continuing source of dissolved-phase BTEX. Based on this experience, most groundwater and remediation professionals reject pump-and-treat as a viable remedial option, except in situations where controlling groundwater movement is the predominant goal.

  17. Treatment of Methyl tert-Butyl Ether Vapors in Biotrickling Filters. 1.

    E-Print Network [OSTI]

    An aerobic microbial consortium able to biodegrade methyl tert-butyl ether (MTBE) was enriched in two waste, the two laboratory- scale biotrickling filters were able to degrade up to 50 g of MTBE per cubic meter be sustained for at least 4-6 weeks. After the acclimation phase, the MTBE degrading biotrickling filters were

  18. Water Research 37 (2003) 37563766 Seasonal and daily variations in concentrations of methyl-

    E-Print Network [OSTI]

    Toran, Laura

    - tertiary-butyl ether (MTBE) at Cranberry Lake, New Jersey Laura Torana, *, Charles Lipkaa , Arthur Baehrb; accepted 24 March 2003 Abstract Methyl-tertiary-butyl ether (MTBE), an additive used to oxygenate gasoline of gasoline-powered watercraft. This paper documents and explains both seasonal and daily variations in MTBE

  19. Synthesis of MTBE during CO hydrogenation: Reaction sites required

    SciTech Connect (OSTI)

    Kazi, A.M.; Goodwin, J.G. Jr.; Marcelin, G.; Oukaci, R. [Univ. of Pittsburgh, PA (United States). Dept. of Chemical and Petroleum Engineering

    1995-03-01T23:59:59.000Z

    Synthesis of methyl tert-butyl ether (MTBE) during carbon monoxide (CO) hydrogenation has been studied with the following reaction schemes: (1) the addition of isobutylene during CO hydrogenation over metal catalysts active for methanol synthesis (Pd/SiO{sub 2} and Li-Pd/SiO{sub 2}) and (2) the addition of isobutylene during CO hydrogenation over a dual bed configuration consisting of Li-Pd/SiO{sub 2} and a zeolite (H-ZSM-5 or HY). The addition of isobutylene during methanol synthesis over the supported Pd catalysts indicated that MTBE cannot be formed on metal sites from a reaction of isobutylene with methanol precursors. However, addition of isobutylene to the syngas feed over a dual bed consisting of a methanol synthesis catalyst and an acid zeolite downstream of the methanol synthesis catalyst showed that MTBE can be synthesized during CO hydrogenation provided acid sites are available. In order to get higher conversions of methanol to MTBE, optimization of the acid catalyst and/or reaction conditions would be required to minimize formation of byproduct hydrocarbons.

  20. Lyondell`s new isobutylene route could fuel an MTBE capacity boost

    SciTech Connect (OSTI)

    Rotman, D.; Wood, A.

    1992-03-25T23:59:59.000Z

    Driven by the hot growth prospects for methyl tert-butyl ether (MTBE), Lyondell Petrochemical (Houston) has developed a route to isobutylene it claims can produce the MTBE feedstock at half the capital cost of alternative synthesis technology. If proved, the process will be used in a new 7500-10,000 bbl/day MTBE plant at Channelview, TX. Lyondell also hopes to license the technology. {open_quotes}With expanding MTBE capacity, we will have to have new routes to isobutylene,{close_quotes} says Bob G. Gower, president and CEO of Lyondell. {open_quotes}We think this is a good fit within Lyondell, but also that it is important technology.{close_quotes} Gower declines to detail its specifics, but says it is a one-step isomerization of n-butenes to isobutylene. The firm has tested the process at a pilot unit and plans a demonstration unit in 1992.

  1. MTBE will be a boon to U. S. gas processors

    SciTech Connect (OSTI)

    Otto, K.W. (Purvin and Gertz, Inc. Dallas, TX (United States))

    1993-01-11T23:59:59.000Z

    This paper reports that the advent of methyl tertiary butyl ether (MTBE) as the primary oxygenate blending component for oxygenated and reformulated motor fuels promises significant benefits for the U.S. gas-processing industry. Increased demand for isobutane as MTBE-plant feedstock will buoy both normal butane and isobutane pricing in U.S. gulf Coast during the 1990s. Elimination of the need to crack normal butane in U.S. olefin plants will also strengthen competitive feedstocks somewhat, including ethane and propane. And increased use of normal butane as isomerization feedstock will result in wider recognition of the premium quality of gas plant normal butane production compared to most refinery C[sub 4] production.

  2. MTBE movements between Texas Gulf Coast plants to be enhanced

    SciTech Connect (OSTI)

    Not Available

    1992-07-27T23:59:59.000Z

    This paper reports that Texas Eastern Products Pipeline Co. (Teppco), Houston, has begun construction of its shuttle pipeline, a 10-mile, 6 and 8-in. line to move methyl tertiary butyl ether (MTBE) between producers and refiners along the Houston Ship Channel. Funding for the project has been approved, rights-of-way are secured, and procurement of materials is under way, according to Teppco. The line will flow from the western edge of Shell's refinery eastward to storage facilities of Teppco's Baytown terminal. The shuttle pipeline anticipates the US requirement for oxygenated gasolines that takes effect Nov. 1. Approximately 70% of the available US merchant capacity for MTBE is located along the shuttle's path, Teppco says.

  3. Treatment of methyl t-butyl ether contaminated water using a dense medium plasma reactor, a mechanistic and kinetic investigation

    E-Print Network [OSTI]

    Dandy, David

    and oxidation mechanisms of methyl t-butyl ether (MTBE) in a dense medium plasma (DMP) reactor utilizing gas for the removal of MTBE from an aqueous solution in the DMP reactor. Rate constants are also derived for three reactor configurations and two pin array spin rates. The oxidation products from the treatment of MTBE

  4. Role of Volatilization in Changing TBA and MTBE Concentrations at

    E-Print Network [OSTI]

    Role of Volatilization in Changing TBA and MTBE Concentrations at MTBE-Contaminated Sites J U A N tertiary butyl ether (MTBE) added to gasoline. Frequent observations of high TBA, and especially rising TBA/MTBE of MTBE to TBA. Typically overlooked is the role of volatilization in the attenuation of these chemicals

  5. The Social Costs of an MTBE Ban in California

    E-Print Network [OSTI]

    Rausser, Gordon C.; Adams, Gregory D.; Montgomery, W. David; Smith, Anne E.

    2005-01-01T23:59:59.000Z

    349 The Social Costs of an MTBE Ban in California REFERENCESD.E. Rolston. Impacts of MTBE on California Groundwater. Environmental Assessment of MTBE, Vol. 4. A. Keller et al. ,

  6. 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. [Robert S. Kerr Environmental Research Center, Ada, OK (United States)

    2009-03-01T23:59:59.000Z

    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.

  7. MTBE catalyst shows increased conversion in commercial unit

    SciTech Connect (OSTI)

    Not Available

    1994-10-10T23:59:59.000Z

    Rising demand for methyl tertiary butyl ether (MTBE) has spawned interest in finding a cost-effective means of increasing production from existing units. A commercial trial of an improved MTBE catalyst was conducted recently at Lyondell Petrochemical Co.'s Channelview, Tex., plant. The new catalyst called Amberlyst 35 Wet, enhanced oxygenate production in the Lyondell trial. The new catalyst changes the activity coefficients of at least one of the components of the MTBE reaction, resulting in higher equilibrium conversion relative to its first-generation counterpart. Key catalyst properties are: particle size, 0.4--1.25 mm; Apparent density, 0.82 g/ml; Surface area, 44 sq m/g; Moisture content, 56%; Concentration of acid sites, 1.9 meq/ml (5.4 meq/g); Porosity, 0.35 cc/g; and Average pore diameter, 300 [angstrom]. Suggested operating conditions are: maximum temperature, 284 F (140 C); minimum bed depth, 24 in. (0.61 m); and liquid hourly space velocity (LHSV), 1--5 hr[sup [minus]1].

  8. Removal of MTBE and other organic contaminants from water by sorption to high silica zeolites

    SciTech Connect (OSTI)

    Anderson, M.A.

    2000-02-15T23:59:59.000Z

    Select zeolites with high SiO{sub 2}/Al{sub 2}O{sub 3} ratios were shown to effectively remove methyl tert-butyl ether (MTBE), chloroform, and trichloroethylene (TCE) from water. In laboratory studies using batch sorption equilibria, high Si large-port mordenite and ZSM-5 (silicalite) were found to have sorption properties for MTBE and TCE superior to activated carbon. for example, at an equilibrium solution concentration of 100 {micro}g/L, high Si mordenite retained 8--12x more MTBE than either of two powdered activated carbons used as reference sorbents. Sorption results also highlight the importance of pore size and SiO{sub 2}/Al{sub 2}O{sub 3} ration on contaminant removal efficiencies by zeolites.

  9. Aerobic mineralization of MTBE and tert-butyl alcohol by stream-bed sediment microorganisms

    SciTech Connect (OSTI)

    Bradley, P.M.; Landmeyer, J.E.; Chapelle, F.H. [Geological Survey, Columbia, SC (United States)] [Geological Survey, Columbia, SC (United States)

    1999-06-01T23:59:59.000Z

    Microorganisms indigenous to the stream-bed sediments at two gasoline-contaminated groundwater sites demonstrated significant mineralization of the fuel oxygenates, methyl tert-butyl ether (MTBE) and tert-butyl alcohol (TBA). Up to 73% of [U-{sup 14}C]-MTBE and 84% of [U-{sup 14}C]-TBA were degraded to {sup 14}CO{sub 2} under mixed aerobic/anaerobic conditions. No significant mineralization was observed under strictly anaerobic conditions. The results indicate that, under the mixed aerobic/anaerobic conditions characteristic of stream-bed sediments, microbial processes may provide a significant environmental sink for MTBE and TBA delivered to surface water bodies by contaminated groundwater or by other sources.

  10. Review of the environmental behavior and fate of methyl tert-butyl ether

    SciTech Connect (OSTI)

    Squillace, P.J.; Zogorski, J.S. [Geological Survey, Rapid City, SD (United States); Pankow, J.F. [Oregon Graduate Inst. of Science and Technology, Beaverton, OR (United States). Dept. of Environmental Science and Engineering; Korte, N.E. [Oak Ridge National Lab., TN (United States). Environmental Science Div.

    1997-09-01T23:59:59.000Z

    A review of pertinent equations and current research indicates that when gasoline oxygenated with methyl tert-butyl ether (MTBE) comes into contact with water, large amounts of MTBe can dissolve. At 25 C, the water solubility of MTBE is about 5,000 mg/L for a gasoline that is 10% MTBE by weight, whereas for a nonoxygenated gasoline, the total hydrocarbon solubility in water is typically about 120 mg/L. Methyl tert-butyl ether sorbs only weakly to subsurface solids; therefore, sorption does not substantially retard the transport of MTBE by ground water. In addition, MTBE generally resists biodegradation in ground water. The half-life of MTBE in the atmosphere can be as short as 3 d in a regional airshed. In the air, MTBE tends to partition into atmospheric water, including precipitation. However, the washing out of gas-phase MTBE by precipitation will not, by itself, greatly alter the gas-phase concentration of the compound in the air. The partitioning of MTBE to precipitation can nevertheless result in concentrations as high as 3 {micro}g/L or more in urban precipitation and can contribute to the presence of MTBE in surface and ground water.

  11. MTBE demand as a oxygenated fuel additive

    SciTech Connect (OSTI)

    NONE

    1996-10-01T23:59:59.000Z

    The MTBE markets are in the state of flux. In the U.S. the demand has reached a plateau while in other parts of the world, it is increasing. The various factors why MTBE is experiencing a global shift will be examined and future volumes projected.

  12. The social costs of an MTBE ban in California (Condensed version)

    E-Print Network [OSTI]

    Rausser, Gordon C.; Adams, Gregory D.; Montgomery, W. David; Smith, Anne E.

    2002-01-01T23:59:59.000Z

    in Focus: Phasing Out MTBE in Gasoline," Annual Energyand P. J. Bartholomae, "MTBE and Benzene Plume Behavior: ASoil Sediment & Groundwater MTBE Special Issue, March, 43-

  13. Interdisciplinary investigation of subsurface contaminant transport and fate at point-source releases of gasoline containing MTBE

    SciTech Connect (OSTI)

    Buxton, H.T.; Baehr, A.L. [Geological Survey, West Trenton, NJ (United States); Landmeyer, J.E. [Geological Survey, Columbia, SC (United States)] [and others

    1997-12-31T23:59:59.000Z

    Methyl tert-butyl ether (MTBE) is commonly found at concentrations above the current U.S. Environmental Protection Agency draft lifetime health advisory for drinking water (20 to 200 micrograms per liter) at many point-source gasoline release sites. MTBE is significantly more persistent than benzene, toluene, ethyl-benzene and xylenes (BTEX) in the subsurface. Therefore, evaluation of the implications of its presence in gasoline to monitored natural attenuation and engineered bioremediation alternatives is warranted. An interdisciplinary, field-based investigation of the subsurface transport and fate of MTBE and petroleum hydrocarbons is being conducted by the U.S. Geological Survey (USGS) Toxic Substances Hydrology Program at the site of an underground gasoline storage-tank release near Beaufort, South Carolina. The objective of the investigation is to provide a systematic evaluation of natural attenuation of MTBE compared to BTEX. Results of the field and laboratory studies at this site will be generalized to a broader range of hydrogeochemical conditions through experiments at other sites. Furthermore, newly developed methods of analysis can be applied to sites across the Nation. This investigation of MTBE at point-source release sites is coordinated with investigations of the occurrence of MTBE in shallow ground water, surface water, precipitation, and the atmosphere being conducted by the USGS National Water-Quality Assessment Program.

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

    SciTech Connect (OSTI)

    Arletti, Rossella, E-mail: rossella.arletti@unito.it [Department of Earth Sciences, University of Torino Via Valperga Caluso 35, I-10125, Torino (Italy)] [Department of Earth Sciences, University of Torino Via Valperga Caluso 35, I-10125, Torino (Italy); Martucci, Annalisa; Alberti, Alberto [Department of Earth Sciences, University of Ferrara, Via G. Saragat 1, I-44100, Ferrara (Italy)] [Department of Earth Sciences, University of Ferrara, Via G. Saragat 1, I-44100, Ferrara (Italy); Pasti, Luisa; Nassi, Marianna [Department of Chemistry, University of Ferrara, Via L. Borsari 26, I-44100 Ferrara (Italy)] [Department of Chemistry, University of Ferrara, Via L. Borsari 26, I-44100 Ferrara (Italy); Bagatin, Roberto [Research Centre for Non-Conventional Energy-Istituto ENI Donegani, Environmental Technologies, Via Fauser 4, I-28100 Novara (Italy)] [Research Centre for Non-Conventional Energy-Istituto ENI Donegani, Environmental Technologies, Via Fauser 4, I-28100 Novara (Italy)

    2012-10-15T23:59:59.000Z

    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.

  15. Multiple steady states during reactive distillation of methyl tert-butyl ether

    SciTech Connect (OSTI)

    Nijhuis, S.A. (Univ. of Amsterdam (Netherlands). Chemical Engineering Dept.); Kerkhof, F.P.J.M.; Mak, A.N.S. (Comprimo Engineers and Contractors, Amsterdam (Netherlands))

    1993-11-01T23:59:59.000Z

    This paper presents results of computer simulations of the synthesis of methyl tert-butyl ether (MTBE) in a fixed-bed reactor and in a reactive distillation column. These calculations clearly showed the advantages of MTBE synthesis in a catalytic distillation tower. Furthermore, the computer simulations showed that multiple steady states may occur in the reactive distillation column during MTBE synthesis in a broad range of operating conditions. An analysis of some sensitivity studies is presented.

  16. Two US markets, or one? How the MTBE-gasoline relationship is evolving

    SciTech Connect (OSTI)

    NONE

    1996-01-26T23:59:59.000Z

    This issue of Energy Detente features the price sensitivity of Methyl Tertiary Butyl Ether. Data is presented for US wholesale gasoline prices vs. MTBE for the 20-month period beginning in June 1994 and ending in January 1996, and the data is discussed. Also contained in this issue is the refining netback data and the fuel price/tax data for the period ending January 5, 1996.

  17. The Social Costs of an MTBE Ban in California

    E-Print Network [OSTI]

    Rausser, Gordon C.; Adams, Gregory D.; Montgomery, W. David; Smith, Anne E.

    2005-01-01T23:59:59.000Z

    85 MTBE is more soluble in water than BTEX, which means thatlong as BTEX plumes; and California Regional Water QualityMTBE than BTEX dissolves in a given quantity of water. This

  18. A screening model for evaluating the degradation and transport of MTBE and other fuel oxygenates in the subsurface

    SciTech Connect (OSTI)

    Sun, Y; Lu, X

    2004-04-20T23:59:59.000Z

    Methyl tert-butyl ether (MTBE) has received high attention as it contributed to cleaner air and contaminated thousands of underground storage tank sites. Because MTBE is very water soluble, it is more difficult to remove from water by conventional remediation techniques. Therefore, biodegradation of MTBE has become a remediation alternative. In order to understand the transport and transformation processes, they present a closed form solution as a screening tool in this paper. The possible reaction pathways of first-order reactions are described as a reaction matrix. The singular value decomposition is conducted analytically to decouple the partial differential equations of the multi-species transport system coupled by the reaction matrix into multiple independent subsystems. Therefore, the complexity of mathematical description for the reactive transport system is significantly reduced and analytical solutions may be previously available or easily derived.

  19. High-temperature ignition of propane with MTBE as an additive: Shock-tube experiments and modeling

    SciTech Connect (OSTI)

    Gray, J.A. (Sandia National Labs., Livermore, CA (United States)); Westbrook, C.K. (Lawrence Livermore National Lab., CA (United States))

    1991-01-01T23:59:59.000Z

    Ignition of propane has been studied in a shock tube and by computational modeling to determine the effect of methyl tert-butyl ether (MTBE) as a fuel additive. MTBE and isobutene were added in amounts up to 25% of the fuel to propane-oxygen-argon mixtures in shock-tube experiments covering a range of temperatures between 1450 and 1800 K. Ignition delays were measured from chemiluminescence at 432 nm due to excited CH radicals. The temperature dependence of the ignition rates was analyzed to yield Arrhenius parameters of E{sub a}{approximately}40 kcal/mol and log (A){approximately} 9.0 sec{sup {minus}1} for the overall reaction. Reactions involving MTBE and its decomposition products were combined with an established propane mechanism in a numerical model to describe the kinetic interaction of this additive with a typical hydrocarbon fuel. The experiments and the kinetic model both show that MTBE and isobutene retard propane ignition with nearly equal efficiency. The kinetic model demonstrates that isobutene kinetics are responsible for inhibition by both MTBE and isobutene, and the specific elementary reactions which produce this behavior are identified.

  20. High-temperature ignition of propane with MTBE as an additive: Shock-tube experiments and modeling. Revision 1

    SciTech Connect (OSTI)

    Gray, J.A. [Sandia National Labs., Livermore, CA (United States); Westbrook, C.K. [Lawrence Livermore National Lab., CA (United States)

    1991-12-01T23:59:59.000Z

    Ignition of propane has been studied in a shock tube and by computational modeling to determine the effect of methyl tert-butyl ether (MTBE) as a fuel additive. MTBE and isobutene were added to amounts up to 25% of the fuel to propane-oxygen-argon mixtures to shock-tube experiments covering a range of temperatures between 1450 and 1800 K. Ignition delays were measured from chemiluminescence at 432 nm due to excited CH radicals. The temperature dependence of the ignition rates was analyzed to yield Arrhenium parameters of E{sub a}{sup {minus}}40 kcal/mol and log(A) {sup {minus}}9.0 sec{sup {minus}1} for the overall reaction. Reactions involving MTBE and its decomposition products were combined with an established propane mechanism in a numerical model to describe the kinetic interaction of this additive with a typical hydrocarbon fuel. The experiments and the kinetic model both show that MTBE and isobutene retard propane ignition with nearly equal efficiency. The kinetic model demonstrates that isobutene kinetics are responsible for inhibition by both MTBE and isobutene, and the specific elementary reactions which produce this behavior are identified. 19 refs., 1 fig., 3 tabs.

  1. High-temperature ignition of propane with MTBE as an additive: Shock-tube experiments and modeling

    SciTech Connect (OSTI)

    Gray, J.A. [Sandia National Labs., Livermore, CA (United States); Westbrook, C.K. [Lawrence Livermore National Lab., CA (United States)

    1991-12-31T23:59:59.000Z

    Ignition of propane has been studied in a shock tube and by computational modeling to determine the effect of methyl tert-butyl ether (MTBE) as a fuel additive. MTBE and isobutene were added in amounts up to 25% of the fuel to propane-oxygen-argon mixtures in shock-tube experiments covering a range of temperatures between 1450 and 1800 K. Ignition delays were measured from chemiluminescence at 432 nm due to excited CH radicals. The temperature dependence of the ignition rates was analyzed to yield Arrhenius parameters of E{sub a}{approximately}40 kcal/mol and log (A){approximately} 9.0 sec{sup {minus}1} for the overall reaction. Reactions involving MTBE and its decomposition products were combined with an established propane mechanism in a numerical model to describe the kinetic interaction of this additive with a typical hydrocarbon fuel. The experiments and the kinetic model both show that MTBE and isobutene retard propane ignition with nearly equal efficiency. The kinetic model demonstrates that isobutene kinetics are responsible for inhibition by both MTBE and isobutene, and the specific elementary reactions which produce this behavior are identified.

  2. High-temperature ignition of propane with MTBE as an additive: Shock-tube experiments and modeling

    SciTech Connect (OSTI)

    Gray, J.A. (Sandia National Labs., Livermore, CA (United States)); Westbrook, C.K. (Lawrence Livermore National Lab., CA (United States))

    1991-12-01T23:59:59.000Z

    Ignition of propane has been studied in a shock tube and by computational modeling to determine the effect of methyl tert-butyl ether (MTBE) as a fuel additive. MTBE and isobutene were added to amounts up to 25% of the fuel to propane-oxygen-argon mixtures to shock-tube experiments covering a range of temperatures between 1450 and 1800 K. Ignition delays were measured from chemiluminescence at 432 nm due to excited CH radicals. The temperature dependence of the ignition rates was analyzed to yield Arrhenium parameters of E{sub a}{sup {minus}}40 kcal/mol and log(A) {sup {minus}}9.0 sec{sup {minus}1} for the overall reaction. Reactions involving MTBE and its decomposition products were combined with an established propane mechanism in a numerical model to describe the kinetic interaction of this additive with a typical hydrocarbon fuel. The experiments and the kinetic model both show that MTBE and isobutene retard propane ignition with nearly equal efficiency. The kinetic model demonstrates that isobutene kinetics are responsible for inhibition by both MTBE and isobutene, and the specific elementary reactions which produce this behavior are identified. 19 refs., 1 fig., 3 tabs.

  3. Multivariable controller increased MTBE complex capacity

    SciTech Connect (OSTI)

    Robertson, D.; Peterson, T.J.; O`Connor, D. [DMC Corp., Houston, TX (United States); Payne, D.; Adams, V. [Valero Refining Co., Corpus Christi, TX (United States)

    1997-03-01T23:59:59.000Z

    Capacity increased by more than 4.6% when one dynamic matrix multivariable controller began operating in Valero Refining Company`s MTBE production complex in Corpus Christi, Texas. This was on a plant that was already running well above design capacity due to previously made process changes. A single controller was developed to cover an isobutane dehydrogenation (ID) unit and an MTBE reaction and fractionation plant with the intermediate isobutylene surge drum. The overall benefit is realized by a comprehensive constrained multivariable predictive controller that properly handles all sets of limits experienced by the complex, whether limited by the front-end ID or back-end MTBE units. The controller has 20 manipulated, 6 disturbance and 44 controlled variables, and covers widely varying dynamics with settling times ranging from twenty minutes to six hours. The controller executes each minute with a six hour time horizon. A unique achievement is intelligent surge drum level handling by the controller for higher average daily complex capacity as a whole. The ID unit often operates at simultaneous limits on reactor effluent compressor capacity, cold box temperature and hydrogen/hydrocarbon ratio, and the MTBE unit at impurity in butene column overhead as well as impurity in MTBE product. The paper discusses ether production, isobutane dehydrogenation, maximizing production, controller design, and controller performance.

  4. Disposition, metabolism, and toxicity of methyl tertiary butyl ether, an oxygenate for reformulated gasoline

    SciTech Connect (OSTI)

    Hutcheon, D.E.; Hove, W. ten; Boyle, J. III [UMDNJ, New Jersey Medical Schook, Newark, NJ (United States)] [UMDNJ, New Jersey Medical Schook, Newark, NJ (United States); Arnold, J.D. [Arnold & Arnold, Inc., Kansas City, MO (United States)] [Arnold & Arnold, Inc., Kansas City, MO (United States)

    1996-04-05T23:59:59.000Z

    Studies of the toxicology of methyl tertiary butyl ether (MTBE) were reviewed as a possible information base for evaluating the health effects of evaporative emissions from reformulated gasoline (RFG). Perirenal fat/blood MTBE concentration ratios ranged from 9.7 to 11.6 after 15 wk of intermittent exposure. During an oxyfuels program in Fairbanks, AK, blood levels of occupationally exposed workers were 0.2-31.5 {mu}g/L MTBE and 1.6 to 72.2 {mu}g/L TBA with a mean TBA:MTBE blood concentration ratio of 4.2. In patients who received MTBE by percutaneous, transhepatic puncture for the dissolution of cholesterol gallstones, concentrations of MTBE in fat tissue reached 60 and 300 {mu}g/g at a treatment time when mean blood MTBE was less than 20 {mu}g/ml. The results of laboratory and clinical studies indicate that metabolites of MTBE may contribute to the nephropathy, neoplasms, and other pathological changes associated with repeated exposure to MTBE in experimental animals. It is concluded that such studies can provide a well-defined database for quantitatitive safety comparisons and health risk-benefit analyses of MTBE and other oxygenates in RFG. 39 refs., 1 tab.

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

    SciTech Connect (OSTI)

    Scott G. Huling; Patrick K. Jones; Tony R. Lee [U.S. Environmental Protection Agency, Ada, OK (United States). Office of Research and Development, National Risk Management Research Laboratory

    2007-06-01T23:59:59.000Z

    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.

  6. Texas plant will use new process to coproduce propylene oxide, MTBE

    SciTech Connect (OSTI)

    Rhodes, A.K.

    1993-08-30T23:59:59.000Z

    Texaco Chemical Co. is building a $400 + million facility to produce 1.2 billion lb/year (14,000 b/d) methyl tertiary butyl ether (MTBE) and 400 million lb/year (about 500 metric tons/day) propylene oxide (PO). The facility-under construction at Port Neches, Tex.-will utilize a newly developed Texaco process that coproduces the two chemicals. The process produces propylene oxide and tertiary butyl alcohol (TBA) from the reaction of isobutane with oxygen in one step, then in a second step with propylene. The TBA is then reacted with methanol in a one-step process that synthesizes MTBE. The paper describes the Port Neches facilities, construction schedule, feedstocks, product uses, and auxiliary equipment.

  7. Gas phase synthesis of MTBE on triflic-acid-modified zeolites

    SciTech Connect (OSTI)

    Nikolopoulos, A.A.; Kogelbauer, A.; Goodwin, J.G. Jr. [Univ. of Pittsburgh, PA (United States)] [and others] [Univ. of Pittsburgh, PA (United States); and others

    1996-01-01T23:59:59.000Z

    The gas phase synthesis of MTBE (methyl tert-butyl ether) was studied using three series of triflic acid (TFA)-modified zeolites, the parent materials being HY, H-mordenite, and HZSM-5. Impregnation with TFA was found to enhance MTBE synthesis activity only for the large-pore zeolite Y and only up to a certain extent of modification. A high level of TFA modification caused a reduction in activity, apparently due to blockage of the active sites by TFA molecules and extra-lattice Al formed during the modification process. The mechanism of activity enhancement by TFA modification appears to be related to the formation of extra-lattice Al rather than the direct presence of TFA. 20 refs., 6 figs., 1 tab.

  8. active methyl tert-butyl: Topics by E-print Network

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

    by Fusarium solani CiteSeer Summary: Fusarium solani degraded methyl tert-butyl ether (MTBE) and other oxygenated compounds from gasoline including tert-butyl alcohol (TBA). The...

  9. Production of methyl tert-alkyl ethers

    SciTech Connect (OSTI)

    Trofimov, V.A.

    1995-01-01T23:59:59.000Z

    The transition to the use of unleaded gasolines has required the replacement of tetraethyl lead by oxygen-containing compounds such as methanol, ethanol, and ethers, which are termed {open_quotes}oxygenates{close_quotes} in the technical literature. These may be used in commercial gasolines in amounts of 10-15% by volume, equivalent to 2% oxygen by weight. When methyl tert-butyl ether (MTBE) is used, the oxygen content may amount to 2.7% by weight. This oxygenate gives a significant improvement of knock resistance of naphtha fractions, the greatest effects being observed for straight-run naphthas and reformer naphthas produced under normal conditions; the MTBE also improves the engine power and economy characteristics and lowers the carbon monoxide content in the exhaust by 15-30% and the hydrocarbon content by 7-8%. This paper describes methods for the production of MTBE and also methyl tert-alkyl ethers.

  10. Toxicity of methyl tertiary butyl ether to Daphnia magna and photobacterium phosphoreum

    SciTech Connect (OSTI)

    Gupta, G.; Lin, Y.J. [Univ. of Maryland Eastern Shore, Princess Anne, MD (United States)

    1995-10-01T23:59:59.000Z

    Methyl tertiary butyl ether (MTBE) is a liquid organic compound added to gasoline to increase its oxygen content and to reduce the emission of carbon monoxide during combustion in many urban areas. In order to meet the 1990 Clean Air Act amendments, gasoline must contain 2.7% oxygen (by weight) or 15% (by volume) of MTBE in gasoline to meet the regulations for the control of carbon monoxide emissions. Health effects caused by inhalation of MTBE include headaches, dizziness, irritated eyes and nausea; MTBE is one of cancer--causing chemicals. Intracaval injection of MTBE (0.2 mg/kg) caused the highest mortality (100%) in rats. General anesthetic effect induced by MTBE was found at or above 1200 mg/kg body weight; Rosenkranz and Klopman (1991) predicted that MTBE is neither a genotoxicant nor a carcinogen. Nevertheless, the safety of using MTBE in oxygenated fuels is now being questioned from its potential as groundwater pollutant. This study measures the toxicity of MTBE to Daphnia magna and Photobacterium phosphoreum. 13 refs.

  11. Observation on the biodegradation and bioremediation potential of methyl t-butyl ether

    SciTech Connect (OSTI)

    Salanitro, J.; Wisniewski, H.; McAllister, P. [Shell Development Co., Houston, TX (United States)

    1995-12-31T23:59:59.000Z

    There have been few reports documenting evidence for the biodegradation of the fuel oxygenate alkyl ether, methyl t-butyl ether (MTBE) in groundwater, soils, and biosludges. Partial (or complete) microbial breakdown of MTBE has been observed in an anaerobic subsoil, a river sediment under methanogenic conditions, a cyclohexane-degrading bacterial consortium and a pure culture of the methylotroph, Methylisnus trichosporium OB3b. An aerobic bacterial enrichment (BC-1) isolated from an industrial transient (non-accumulating) metabolic intermediate. The studies suggest that MTBE is cleaved by BC-1 to TBA which is then metabolized via isopropanol and acetone. There is little information on the occurrence of indigenous MTBE-degraders in groundwater, soils and activated sludges. Preliminary evidence has been obtained, however, from a marketing terminal groundwater site that naturally-occurring MTBE-degraders are present in some monitoring wells. Microcosm experiments with groundwater from this aquifer show that MTBE is aerobically degraded (no TBA formed) with a first-order decay rate (0.31/day) similar to BTEX. Also, MTBE did not inhibit the intrinsic biodegradation potential of BTEX in groundwater microcosms. In summary, the data presented indicate that MTBE biodegradation has been observed in some environmental media. Further work is needed to assess the feasibility of using indigenous or derived aerobic and anaerobic MTBE-degrading cultures for treating fuel ethers in groundwaters or wastewater with in-situ or ex-situ bioremediation technologies.

  12. Biodegradation of methyl tert-butyl ether by a bacterial pure culture

    SciTech Connect (OSTI)

    Hanson, J.R.; Ackerman, C.E.; Scow, K.M.

    1999-11-01T23:59:59.000Z

    A bacterial strain, PM1, which is able to utilize methyl tert-butyl ether (MTBE) as its sole carbon and energy source, was isolated from a mixed microbial consortium in a compost biofilter capable of degrading MTBE. Initial linear rates of MTBE degradation by 2 x 10{sup 6} cells ml{sup {minus}1} were 0.07, 1.17, and 3.56 {mu}g ml{sup {minus}1} h{sup {minus}1} for initial concentrations of 5, 50, and 500 {mu}g MTBE ml{sup {minus}1}, respectively. When incubated with 20 {mu}g of uniformly labeled [{sup 14}C]MTBE ml{sup {minus}1}, strain PM1 converted 46% to {sup 14}CO{sub 2} and 19% to {sup 14}C-labeled cells within 120 h. This yield is consistent with the measurement of protein accumulation at different MTBE concentrations from which was estimated a biomass yield of 0.18 of cells mg MTBE{sup {minus}1}. Strain PM1 was inoculated into sediment core material collected from a contaminated groundwater plume at Port Hueneme, California, in which there was no evidence of MTBE degradation. Strain PM1 readily degraded 20 {micro}g of MTBE ml{sup {minus}1} added to the core material. The rate of MTBE removal increased with additional inputs of 20 {micro}g of MTBE ml{sup {minus}1}. These results suggest that PM1 has potential for use in the remediation of MTBE-contaminated environments.

  13. Remediation of a fractured clay soil contaminated with gasoline containing MTBE

    SciTech Connect (OSTI)

    Johnson, R.L.; Grady, D.E. [Oregon Graduate Institute, Portland, OR (United States); Walden, T. [BP Oil Europe, Brussels (Belgium)

    1997-12-31T23:59:59.000Z

    Gasoline and other light non-aqueous phase liquids (LNAPLs) released into fractured clay soils initially move by advection of the LNAPL through the fractures. Once advective movement of the LNAPL ceases, dissolution of the gasoline components into the pore water and diffusion into the intact blocks of clay becomes an important transport process. The aqueous-phase flux of each compound in the mixture depends in large part upon its aqueous solubility. For example, a low-solubility compound like isooctane remains primarily in the fracture in the LNAPL. A high-solubility compound, like methyl-tert-butyl ether (MTBE), dissolves readily and may move almost entirely into the clay matrix. The distribution of compounds between the matrix and the fractures will have an important impact on the rate at which the gasoline contaminated soil can be remediated. In this context, the presence of soluble additives like MTBE can significantly impact the risk and remediation time for the, soil. Beginning in 1993 a field study to examine the applicability of air flushing for remediation of low-permeability soils was sponsored by API. The study focused on a variety of soil vapor extraction (SVE) and in situ air sparging (IAS) approaches for mass removal and risk reduction. The source of gasoline contamination in this study was a release of 50 liters of a mixture containing 14 gasoline hydrocarbons ranging from pentane to naphthalene, and including MTBE. The mixture was released into the shallow subsurface and allowed to redistribute for 10 months prior to air flushing startup. Numerical modeling indicated that essentially all of the MTBE should have dissolved into the matrix. In contrast, essentially all of the isooctane should have remained in the LNAPL in the fractures.

  14. Recovery of methanol in an MTBE process

    SciTech Connect (OSTI)

    Whisenhunt, D.E.; Byers, G.L.; Hattiangadi, U.S.

    1988-05-31T23:59:59.000Z

    In a process for the manufacture of methyltertiarybutylether (MTBE) in which methanol and a mixture of C/sub 4/ hydrocarbons containing isobutylene are contacted in a reaction zone containing an ion-exchange resin catalyst under suitable conditions to effect the reaction of methanol and isobutylene to produce a reaction product containing MTBE, unreacted methanol, unreacted isobutylene and other C/sub 4/ hydrocarbons, the reaction product is introduced to a fractionation zone wherein it is separated into a bottoms product comprising essentially MTBE and an overhead product containing unreacted methanol, unreacted isobutylene, and other C/sub 4/ hydrocarbons, and the overhead product is introduced to an absorption zone wherein the methanol is absorbed; the improvement is described which comprises utilizing silica gel as adsorbent and regenerating the silica gel adsorbent in a closed loop by contacting the silica gel absorbent with a desorption gas stream at an elevated temperature for a sufficient period of time to remove absorbed methanol, cooling the effluent from the adsorption zone to condense desorbed methanol removing desorbed methanol from the system and recycling the desorption gas to the adsorption zone.

  15. Kinetics and mechanism of the sonolytic destruction of methyl tert-butyl ether by ultrasonic irradiation in the presence of ozone

    SciTech Connect (OSTI)

    Kang, J.W. [Yonsei Univ., Wonju (Korea, Republic of). Dept. of Industrial Environment and Health] [Yonsei Univ., Wonju (Korea, Republic of). Dept. of Industrial Environment and Health; Hoffmann, M.R. [California Inst. of Tech., Pasadena, CA (United States). W.M. Keck Labs.] [California Inst. of Tech., Pasadena, CA (United States). W.M. Keck Labs.

    1998-10-15T23:59:59.000Z

    The kinetics and mechanism of the sonolytic degradation of methyl tert-butyl ether (MTBE) have been investigated at an ultrasonic frequency of 205 kHz and power of 200 W L{sup {minus}1}. The observed first-order degradation rate constant for the loss of MTBE increased from 4.1 {times} 10{sup {minus}4} s{sup {minus}1} to 8.5 {times} 10{sup {minus}4} s{sup {minus}1} as the concentration of MTBE decreased from 1.0 to 0.01 mM. In the presence of O{sub 3}, the sonolytic rate of destruction of MTBE was accelerated substantially. The rate of MTBE sonolysis with ozone was enhanced by a factor of 1.5--3.9 depending on the initial concentration of MTBE. tert-Butyl formate, tert-butyl alcohol, methyl acetate, and acetone were found to be the primary intermediates and byproducts of the degradation reaction with yields of 8, 5, 3, and 12%, respectively. A reaction mechanism involving three parallel pathways that include the direct pyrolytic decomposition of MTBE, the direct reaction of MTBE with ozone, and the reaction of MTBE with hydroxyl radical is proposed.

  16. Feasibility of using bioaugmentation with bacterial strain PM1 for bioremediation of MTBE-contaminated vadose and groundwater environments

    E-Print Network [OSTI]

    Scow, Kate M; Hristova, Krassimira

    2001-01-01T23:59:59.000Z

    2000. "In Situ Treatment of MTBE by Biostimulation of NativeAmerican Petroleum Institute MTBE Biodegradation Workshop,Detection and Quantification of MTBE-degrading Strain PM1 by

  17. Feasibility of using bioaugmentation with bacterial strain PM1 for bioremediation of MTBE-contaminated vadose and groundwater environments

    E-Print Network [OSTI]

    Scow, Kate M; Hristova, Krassimira

    2001-01-01T23:59:59.000Z

    Tahoe City, CA. 9/18/00. Bioremediation of MTBE-Contaminated2000, DC Davis, CA Bioremediation of MTBE at Port HeuenemeRiverside. 5/31101 Bioremediation of MTBE through

  18. The Social Costs of an MTBE Ban in California

    E-Print Network [OSTI]

    Rausser, Gordon C.; Adams, Gregory D.; Montgomery, W. David; Smith, Anne E.

    2005-01-01T23:59:59.000Z

    in Gasoline. Annual Energy Outlook 2000. DOE/EIA-0383,in Gaso- line. Annual Energy Outlook 2000. DOE/EIA-0383,MTBE in Gasoline, Annual Energy Outlook 2000, 2001a. Mazur,

  19. Patent Waivers Overview | Department of Energy

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

    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...

  20. Fast photoreactions of ethanol and MTBE on tropospheric metal oxide particles

    SciTech Connect (OSTI)

    Idriss, H.; Seebauer, E.G. [Univ. of Illinois, Urbana, IL (United States)

    1995-12-31T23:59:59.000Z

    Ethanol (EtOH) and tert-Butyl methyl ether (MTBE) are both finding increased use as oxygenated additives to fuels. However, the environmental fate in the troposphere of these species is unclear when they escape as fugitive emissions. In several locations there are reports of human illness in response to MTBE in particular. Volatile organic compounds (VOC`s) such as these are generally thought to react by a variety of homogeneous free-radical mechanisms, usually beginning with attack by OH radical. However, we show by laboratory kinetic studies that the heterogeneous photoreaction on solid suspended metal-oxide particulates such as fly ash proceeds with a comparable rate, especially in urban environments. EtOH reacts to form acetaldehyde, and EtOH forms isobutene, methanol, and formaldehyde. Our work appears to be the first-ever demonstration that VOC`s can react as fast by a heterogeneous mechanism as by a homogeneous one in the atmosphere. Experiments by various optical and kinetic techniques show that the active phases in fly ash are Fe oxides, which are fairly abundant in other atmospheric particulates as well.

  1. Intrinsic bioremediation of a BTEX and MTBE plume under mixed aerobic/denitrifying conditions

    SciTech Connect (OSTI)

    Borden, R.C.; Daniel, R.A. [North Carolina State Univ., Raleigh, NC (United States). Civil Engineering Dept.

    1995-09-01T23:59:59.000Z

    A shallow Coastal Plain aquifer in rural Sampson Country, North Carolina, has been contaminated with petroleum hydrocarbon from a leaking underground storage tank containing gasoline.An extensive field characterization has been performed to define the horizontal and vertical distribution of soluble gasoline components and indicator parameters. A plume of dissolved methyl tert-butyl ether (MTBE) and the aromatic hydrocarbons benzene, toluene, ethylbenzene, and xylene isomers (BTEX) is present in the aquifer and has migrated over 600 ft from the source area. Background dissolved oxygen concentrations range from 7 to 8 mg/L, and nitrate concentrations range from 5 to 22 mg/L as N due to extensive fertilization of fields surrounding the spill. In the center of the BTEX plume, oxygen concentrations decline to less than 1 mg/L while nitrate concentrations remain high. The total mass flux of MTBE and all BTEX components decline with distance downgradient relative to a conservative tracer (chloride). At the source, the total BTEX concentration exceeds 75 mg/L while 130 ft downgradient, total BTEX concentrations are less than 4.9 mg/L, a 15-fold reduction. Toluene and ethylbenzene decline most rapidly followed by m-p-xylene, o-xylene and finally benzene. Biodegradation of TEX appears to be enhanced by the excess nitrate present in the aquifer while benzene biodegradation appears to be due to strictly aerobic processes.

  2. Heterogeneous models of tubular reactors packed with ion-exchange resins: Simulation of the MTBE synthesis

    SciTech Connect (OSTI)

    Quinta Ferreira, R.M.; Almeida-Costa, C.A. [Univ. of Coimbra (Portugal). Dept. of Chemical Engineering; Rodrigues, A.E. [Univ. of Porto (Portugal). Dept. of Chemical Engineering

    1996-11-01T23:59:59.000Z

    The study of behavior of fixed-bed reactors using ion-exchange resins as catalysts was carried out by making use of a complete bidimensional heterogeneous model for the reactor, which included the resistances inside the ion-exchange resin particles, considered with a macroreticular structure. The active sites were located inside the gel phase of the resin, represented by microspheres, and on the macropores walls. The overall efficiency of such heterogeneous catalyst particles was defined by the macroeffectiveness and microeffectiveness factors accounting for the process behavior on the macropores and inside the microspheres. The synthesis of methyl tert-butyl ether, MTBE, a liquid-phase reversible exothermic reaction between methanol and isobutene, was considered as a reference case. This system was studied in the temperature range of 313--338 K, and the effect of the thermodynamic equilibrium conditions was examined. The results predicted by the complete heterogeneous model were compared with those obtained with the simple pseudohomogeneous model, which revealed higher hot spots. Moreover, a comparison between bidimensional and unidimensional models was also performed. The orthogonal collocation method was used for the discretization of the differential equations inside the catalyst particles, which were reduced from three (corresponding to the three mass balances for the three compounds, isobutene, methanol, and MTBE) to only one differential equation, by using the concept of the generalized variable.

  3. Ethanol Waivers: Needed or Irrelevant?

    E-Print Network [OSTI]

    Griffin, James M.; Dahl, Rachel

    regulatory apparatus could accommo- date a substantial ethanol reduction with no need for a waiver. Even if gasoline blenders found it both economically and technically desirable to reduce ethanol consumption, a reduction of 2.6 billion gal- lons... up the price of corn and gasoline blenders will have little choice but to pay the higher ethanol prices. OIL PRICE UNCERTAINTY ARGUES FOR A WAIVER With a 2013 waiver in place, refiners would have time to implement the planning to produce higher...

  4. The social costs of an MTBE ban in California (Long version)

    E-Print Network [OSTI]

    Rausser, Gordon C.; Adams, Gregory D.; Montgomery, W. David; Smith, Anne E.

    2002-01-01T23:59:59.000Z

    Ethanol, Non-oxy Case D'( p) MTBE Case D(p) U.S. Supply S(p)NO. 932 THE SOCIAL COSTS OF AN MTBE BAN IN CALIFORNIA (LONGMTBE .

  5. Atmosphere-Water Interaction of Chloroform, Toluene, and MTBE in Small Perennial Urban Streams

    E-Print Network [OSTI]

    Atmosphere-Water Interaction of Chloroform, Toluene, and MTBE in Small Perennial Urban Streams-butyl ether (MTBE) are frequently detected VOCs in the atmosphere, surface water, and ground water in urban not be the predominant source of chloroform and toluene in the two urban streams. In contrast, MTBE may be coming from

  6. The current status of the U.S. MTBE industry

    SciTech Connect (OSTI)

    Rose, G.M. [Global Octanes Corp., Houston, TX (United States)

    1995-12-31T23:59:59.000Z

    This paper reviews the status of the MTBE industry from its beginnings as a result of the Clean Air Act Amendments and the need for the use of oxygenates in non-attainment areas. During 1990--93 three world scale merchant plants were constructed and in 1994 two more were brought on stream. The paper tabulates reasons why MTBE gained the lion`s share of the oxygenates market. Finally the paper discusses the problems that now plague the industry and their causes.

  7. Reactant adsorption and its impact upon MTBE synthesis on zeolites

    SciTech Connect (OSTI)

    Kogelbauer, A.; Nikolopoulos, A.A.; Goodwin, J.G. Jr.; Marcelin, G. [Univ. of Pittsburgh, PA (United States)] [Univ. of Pittsburgh, PA (United States)

    1995-03-01T23:59:59.000Z

    Zeolites show interesting properties as catalysts for MTBE synthesis from methanol and isobutene such as a high selectivity to MTBE even at a low methanol/isobutene feed ratio. In order to explain this high selectivity, the adsorption behaviors of HY and HZSM-5 zeolites and their impact on activity and selectivity for MTBE synthesis were studied. Adsorption experiments, carried out under conditions similar to those used for reaction, showed that ca. 2.5 molecules of methanol were adsorbed per acid site on HZSM-5 and HY zeolites, whereas isobutene was found to form a 1:1 adsorption complex. The excess methanol adsorbed was found to be only weakly bonded, probably via hydrogen bonds. On a commercially used resin catalyst (Amberlyst-15) equal amounts of methanol and isobutene were adsorbed. The higher methanol uptake of the zeolites was paralleled by a higher selectivity to MTBE as compared to the resin catalyst. The increased adsorption of methanol on the zeolites was concluded to play a key role in suppressing the formation of by-products due to isobutene dimerization or oligomerization by decreasing the adsorption of isobutene on the active sites and thereby keeping these sites available for reaction. 40 refs., 5 figs., 3 tabs.

  8. aerobic mtbe biodegradation: Topics by E-print Network

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

    aerobic mtbe biodegradation First Page Previous Page 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 Next Page Last Page Topic Index 1 Aerobic Biodegradation of...

  9. New low energy process for MTBE and TAME

    SciTech Connect (OSTI)

    Herwig, J.; Schleppinghoff, B.; Schulwitz, S.

    1984-06-01T23:59:59.000Z

    Considered as new bulk petrochemicals of limited feedstocks MTBE (methyltertbutylether) and TAME (tertamylmethylether) need cheap and simple, minimum-cost production processes. The problems in optimizing the etherification are set by specifications for ether products and hydrocarbon raffinates. Working up reaction products from etherification processes containing hydrocarbons, methanol and ether to secure the pure main and side products is difficult because of azeotrope formation of methanol with ethers or hydrocarbons. At EC Erdolchemie GmbH, Cologne, a semicommercial unit with a capacity of 2,500 metric t/y has now been successfully operated for nearly one year producing high purity MTBE (> 99 wt.%) and a raffinate II with methanol content of < 0.05 wt.%. The TAME process has successfully been tested in a 3,000 kg/y TAME pilot plant for almost two years. Based on the operating experience, EC has prepared the engineering for a commercial multiproduct plant, including the production of 30,000 metric t/y MTBE, 15,000 metric t/y TAME and 6,000 metric t/y methylbutenes (TAME cracking product) in the first stage. EC has made application to the authorities for a construction permit. The process for MTBE and TAME will be licensed by EC Erdolchemie GmbH, Postfach 75 20 02, 5000 Cologne 71, West Germany or by Lurgi Kohle und Mineraloltechnik GmbH, Postfach 11 12 31, 6000 Frankfurt Main 2, West Germany.

  10. Kinetics and modeling of mixture effects during complete catalytic oxidation of benzene and methyl tert-butyl ether

    SciTech Connect (OSTI)

    Dangi, S.; Abraham, M.A. [Univ. of Tulsa, OK (United States). Dept. of Chemical Engineering] [Univ. of Tulsa, OK (United States). Dept. of Chemical Engineering

    1997-06-01T23:59:59.000Z

    The performance of a catalytic incinerator depends on the nature of the compounds being oxidized and cannot be predicted simply by knowing the performance of the incinerator with pure-component model compounds. Considering the importance of mixture effects, an attempt was made to develop a combined model to predict the conversion when benzene and methyl tert-butyl ether (MTBE) are simultaneously oxidized. Complete catalytic oxidation of benzene and MTBE, singly and in mixtures, was investigated over a platinum catalyst. No inhibition effects were seen with benzene, but MTBE conversion was distinctly inhibited by benzene. A Mars-van Krevelen rate model was used to explain the results. Model parameters were obtained from pure-component experiments and then incorporated into a multicomponent model without any adjustment or additional rate parameters. The multicomponent model was able to predict the conversion of benzene and MTBE oxidation in the binary mixture using the pure-component data without adjustable parameters.

  11. October 2012 Renewable Fuel Standard Waiver

    E-Print Network [OSTI]

    Noble, James S.

    for four different biofuel categories and their effects on agricultural commodity markets. This report no waiver of the RFS in response to the drought. Analysis reported here estimates the effects of a waiverOctober 2012 Renewable Fuel Standard Waiver Options during the Drought of 2012 FAPRI-MU Report #11

  12. Cytotoxic and DNA-damaging effects of methyl tert-butyl ether and its metabolites on HL-60 cells in vitro

    SciTech Connect (OSTI)

    Tang, G.H. [Xian Medical Univ. (China); Shen, Y.; Shen, H.M. [National Univ. of Singapore (Singapore)] [and others

    1996-12-31T23:59:59.000Z

    Methyl tert-butyl ether (MTBE) is a widely used oxygenate in unleaded gasoline; however, few studies have been conducted on the toxicity of this compound. This study evaluates the cytotoxic and DNA-damaging effects of MTBE and its metabolites in a human haemopoietic cell line, HL-60. The metabolites of MTBE studied include tertiary butyl alcohol (TBA), {alpha}-hydroxyisobutyric acid (HIBA), and formaldehyde. Comet assay is used to assess DNA damage, and the cytotoxicity is investigated by lactate dehydrogenease (LDH) release. The results show no significant cytotoxic effects of MTBE, TBA, and HIBA over a concentration ranging from 1 to 30 mM. Formaldehyde, in contrast, causes a substantial LDH release at a concentration of 5 {mu}M. Hydrogen peroxide, a known oxidative agent, at concentrations ranging from 10 to 100 {mu}M, produces a significant dose-related increase in DNA damage, whereas a much higher concentration of MTBE (1 to 30 mM) is required to produce a similar observation. The genotoxic effects of TBA and HIBA appear to be identical to that of MTBE. Conversely, DNA damage is observed for formaldehyde at a relatively low concentration range (5 to 100 {mu}M). These findings suggest that MTBE and its metabolites, except formaldehyde, have relatively low cytotoxic and genotoxic effects. 16 refs., 4 figs.

  13. The evolution of fuel: A dissertation on MTBE and elastomers

    SciTech Connect (OSTI)

    Smith, G.M. [General Valve Co., Brookshire, TX (United States)

    1995-12-31T23:59:59.000Z

    This paper begins with a history of the development of the internal combustion engine and the need for a fuel octane booster that would also be non-polluting. The use of ethers as fuel additives cause a compatibility problem with valve sealing materials. The main purpose of this presentation is to address this compatibility problem. The paper makes specific recommendations for the author`s General Twin Seal, describing the seal components (slip seal, bonnet and lower plate O-rings, gland O-rings, bearing retainer O-rings, and pressure relief device seals) and which materials these components should be manufactured from to be compatible with the following fuel additives: toluene, MTBE, and various mixtures of toluene and MTBE.

  14. ClassWaiver-PUA.pdf | Department of Energy

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

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

  15. Class_Waiver_NPUA-2.pdf | Department of Energy

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

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

  16. 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.

  17. Memorandum of Decision: Withdrawal of Waiver for Fluorescent...

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

    & Publications Nationwide Categorical Waiver Memorandum of Decision: Withdrawal of LED Lighting Waiver ISSUANCE 2014-12-29: Energy Conservation Program: Clarification for...

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

    Energy Savers [EERE]

    (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...

  19. 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.

  20. 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

    SciTech Connect (OSTI)

    Oh, Keun-Chan; Stringfellow, William T.

    2003-10-02T23:59:59.000Z

    Methyl tert-butyl ether (MTBE) is now one of the most common groundwater contaminants in the United States. Groundwater contaminated with MTBE is also likely to be contaminated with tert-butyl alcohol (TBA), because TBA is a component of commercial grade MTBE, TBA can also be used as a fuel oxygenate, and TBA is a biodegradation product of MTBE. In California, MTBE is subject to reporting at concentrations greater than 3 {micro}g/L. TBA is classified as a ''contaminant of current interest'' and has a drinking water action level of 12 {micro}g/L. In this paper, we describe the development and optimization of a simple, automated solid phase microextraction (SPME) method for the analysis of MTBE and TBA in water and demonstrate the applicability of this method for monitoring MTBE and TBA contamination in groundwater, drinking water, and surface water. In this method, the headspace (HS) of a water sample is extracted with a carboxen/polydimethylsiloxane SPME fiber, the MTBE and TBA are desorbed into a gas chromatograph (GC), and detected using mass spectrometry (MS). The method is optimized for the routine analysis of MTBE and TBA with a level of quantitation of 0.3 {micro}g/L and 4 {micro}g/L, respectively, in water. MTBE quantitation was linear for over two orders of concentration (0.3 {micro}g/L -80 {micro}g/L). TBA was found to be linear within the range of 4 {micro}g/L-7,900 {micro}g/L. The lower level of detection for MTBE is 0.03 {micro}g/L using this method. This SPME method using headspace extraction was found to be advantageous over SPME methods requiring immersion of the fiber into the water samples, because it prolonged the life of the fiber by up to 400 sample analyses. This is the first time headspace extraction SPME has been shown to be applicable to the measurement of both MTBE and TBA at concentrations below regulatory action levels. This method was compared with the certified EPA Method 5030/8260B (purge-and-trap/GC/MS) using split samples from laboratory bioreactors treating MTBE contaminated water and applied to environmental samples collected throughout the East Bay area of California. Results from the SPME-HS/GC/MS method were directly comparable to the EPA Method 5030/8260B. This method provides an simple, inexpensive, accurate, and sensitive alternative to EPA Method 5030/8260B for the analysis of MTBE and TBA in water samples.

  1. Why methyl tert-butyl ether production by reactive distillation may yield multiple solutions

    SciTech Connect (OSTI)

    Hauan, S.; Hertzberg, T.; Lien, K.M. [Univ. of Trondheim (Norway)

    1995-03-01T23:59:59.000Z

    This paper presents an explanation of why methyl tert-butyl ether (MTBE) production by reactive distillation may yield multiple solutions. Widely different composition profiles and conversions may, as already reported by Krishna and others, results with identical column specifications, depending on the initial estimates provided. A hypothesis yielding a qualitative understanding of this phenomenon has been developed. The inert n-butene plays a key role in the proposed explanation: As the reaction mixture is diluted with n-butene, the activity coefficient of methanol increases substantially and the temperature decreases. This dilution has a profound effect on the equilibrium conversion, enabling MTBE to escape from the reactive zone without decomposition. When methanol is fed below or in the lower part of the reactive zone of the column, the ``lifting capacity`` of the minimum boiling point MTBE-methanol azeotrope will also be important.

  2. Pilot-scale evaluation of chemical oxidation for MTBE-contaminated soil

    SciTech Connect (OSTI)

    Rahman, M.; Schupp, D.A.; Krishnan, E.R.; Tafuri, A.N.; Chen, C.T.

    1999-07-01T23:59:59.000Z

    The US Environmental Protection Agency (USEPA) has tentatively classified MTBE as a possible human carcinogen, thus further emphasizing the importance for study of fate, transport, and environmental effects of MTBE. The treatment of subsurface contaminants (e.g., MTBE) from leaking underground storage tank (LUST) sites presents many complex challenges. Many techniques have been employed for the remediation of contaminants in soil and groundwater at LUST sites. Under sponsorship of US EPA's National Risk Management Research Laboratory, IT Corporation has conducted evaluations of chemical oxidation of MTBE contaminated soil using Fenton's Reagent (hydrogen peroxide catalyzed by ferrous sulfate), simulating both ex-situ and in-situ soil remediation. Bench-scale ex-situ tests have shown up to 90% degradation of MTBE within 12 hours. Pilot-scale MTBE oxidation tests were conducted in a stainless paddle-type mixer with a 10 cubic foot mixing volume. The reactor was designed with a heavy duty mixer shaft assembly to homogenize soil and included provisions for contaminant and reagent addition, mixing, and sample acquisition. The tests were performed by placing 400 pounds of a synthetic soil matrix (consisting of a mixture of top soil, sand, gravel and clay) in the reactor, spiking with 20 ppm of MTBE, and mixing thoroughly. The variables evaluated in the pilot-scale tests included reaction time, amount of hydrogen peroxide, and amount of ferrous sulfate. After 8 hours of reaction, using 4 times the stoichiometric quantity of hydrogen peroxide and a 10:1 hydrogen peroxide: ferrous iron weight ratio, approximately 60% MTBE degradation was observed. When 10 times the stoichiometric quantity of hydrogen peroxide was used (with the same ratio of hydrogen peroxide to ferrous iron), 90% MTBE degradation was observed. When the same test was performed without any ferrous iron addition, 75% MTBE degradation was observed.

  3. Exposure to methyl tert-butyl ether and benzene among service station attendants and operators

    SciTech Connect (OSTI)

    Hartle, R. [National Inst. for Occupational Safety and Health, Cincinnati, OH (United States)

    1993-12-01T23:59:59.000Z

    Concerns for atmospheric pollution from auto exhaust have led to the blending of {open_quotes}oxygenates{close_quotes} with motor fuels. The most common oxygenate, methyl tert-butyl ether (MTBE) is currently required within several metropolitan areas (Denver and Phoenix) in the range of 12% of the motor fuel. Amendments to the Clean Air Act may expand this requirement to as many as 44 other areas of the United States in the near future. In consideration of the magnitude of potential uncontrolled exposures from its extensive use and a related concern involving the potential influence of MTBE blending on exposures to other constituents of gasoline (particularly benzene), an evaluation of exposures among service station attendants and operators was undertaken at the request, and in cooperation with, the American Petroleum Institute during the latter part of 1990. For application of the survey results to a broad audience, three categories or types of service stations were identified with regard to MTBE use and exposure potential: (a) service stations that do not use MTBE or use it only as an octane enhancer, (b) service stations with seasonal requirements to use 12-15% MTBE (the Denver, Colorado, and Phoenix, Arizona, metropolitan areas), and (c) service stations equipped with stage II (active) vapor recovery systems (several coastal areas, most notably Southern California). 4 refs., 4 tabs.

  4. Reaction calorimetry study of the liquid-phase synthesis of tert-butyl methyl ether

    SciTech Connect (OSTI)

    Sola, L.; Pericas, M.A.; Cunill, F.; Iborra, M. (Univ. de Barcelona (Spain). Dept. d'Enginyeria Quimica)

    1994-11-01T23:59:59.000Z

    The liquid-phase addition of methanol to isobutene to give tert-butyl methyl ether (MTBE) on the ion-exchange resin Lewatit K2631 has been studied in a calorimetric reactor. Heat capacity of MTBE and enthalpy of the MTBE synthesis reaction in the temperature range 312--333 K have been determined. MTBE heat capacity in the liquid phase has been found to obey the equation c[sub P] (J/mol[center dot]K) = 472.34 [minus] 2.468(T/K) + 0.005071(T/K)[sup 2]. At 298 K the standard molar reaction enthalpy is [Delta]H[degree] = [minus]33.8 kJ/mol. A method to estimate apparent activation energies from heat flow rate in a given reaction has been developed and proved to be valid for the MTBE synthesis. Using this method, an apparent activation energy of 91.1--95.2 kJ/mol is calculated. A [minus]3.8 kJ/mol value has been found for the adsorption enthalpy of methanol on the ion-exchange resin Lewatit K2631 by a combination of reaction calorimetry and thermogravimetry. This allows the calculation of an activation energy on the gel phase of the resin of 91 kJ/mol.

  5. Ethanol Waivers: Needed or Irrelevant?

    E-Print Network [OSTI]

    Boas, Harold P.

    Ethanol Waivers: Needed or Irrelevant? JAMES M. GRIFFIN & RACHAEL DAHL The Mosbacher Institute VOLUME 3 | ISSUE 2 | 2012 2012 RELAXING THE ETHANOL MANDATE The severity of the drought of 2012 affecting for ethanol production, 6.72 BB for domestic food and feed and the remainder for exports (Figure 1). The USDA

  6. Treatment of methyl tert-butyl ether vapors in biotrickling filters. 1. Reactor startup, steady-state performance, and culture characteristics

    SciTech Connect (OSTI)

    Fortin, N.Y.; Deshusses, M.A. [Univ. of California, Riverside, CA (United States). Dept. of Chemical and Environmental Engineering] [Univ. of California, Riverside, CA (United States). Dept. of Chemical and Environmental Engineering

    1999-09-01T23:59:59.000Z

    An aerobic microbial consortium able to biodegrade methyl tert-butyl ether (MTBE) was enriched in two waste air biotrickling filters after continuous operation for 6 months. After this acclimation phase, the two laboratory-scale biotrickling filters were able to degrade up to 50 g of MTBE per cubic meter of reactor per hour, a value comparable to other gasoline constituents. Such high performance could be sustained for at least 4--6 weeks. After the acclimation phase, the MTBE degrading biotrickling filters were characterized by their almost full conversion of MTBE to carbon dioxide and the absence of any degradation byproducts in either the gas or the liquid phase. They also exhibited a very high specific degradation activity per amount of biomass, and a low rate of biomass accumulation. An observed biomass yield of 0.1 g g{sup {minus}1} and a specific growth rate of 0.025 day{sup {minus}1} were determined for the biotrickling filter process culture. Further data on MTBE mass transfer and on the dynamic behavior of the biotrickling filter are presented in part 2 of this paper. Overall, the results demonstrate that MTBE can be effectively biodegraded under carefully controlled environmental conditions.

  7. The Social Costs of an MTBE Ban in California

    E-Print Network [OSTI]

    Rausser, Gordon C.; Adams, Gregory D.; Montgomery, W. David; Smith, Anne E.

    2005-01-01T23:59:59.000Z

    ethyl tertiary butyl ether (ETBE), or tertiary amyl methylOther oxygenates such as ETBE and TAME exist. However, these

  8. New processes to recovery methanol and remove oxygenates from Valero MTBE unit

    SciTech Connect (OSTI)

    Hillen, P.; Clemmons, J.

    1987-01-01T23:59:59.000Z

    The refiner today has to evaluate every available option to increase octane in the gasoline pool to make up for the loss in octane created by lead phase down. Production of MTBE is one of the most attractive options. MTBE is produced by selectivity reacting isobutylene with methanol. Valero Refining's refinery at Corpus Christie, Texas (formerly Saber Refining) is one of the most modern refineries built in the last decade to upgrade resids. As part of the gasoline upgrading Valero had built a Butamer Unit to convert normal butane to isobutane upstream of their HF Alkylation Unit. In 1984 as an ongoing optimization of its operations, Valero Refining evaluated various processes to enable it to increase the octane output, and decided to build an MTBE unit. Valero selected the MTBE process licensed by Arco Technology, Inc. and contracted with Jacobs Engineering Group, Inc., Houston, Texas to provide detailed engineering and procurement services.

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

    SciTech Connect (OSTI)

    Corsi, Dr. Richard [University of Texas, Austin; Morandi, Dr. Maria [University of Texas Health Science Center, Houston; Siegel, Dr. Jeffrey [University of Texas, Austin; Hun, Diana E [ORNL

    2011-01-01T23:59:59.000Z

    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.

  10. Traitement biologique in situ au sein d'un aquifre de polluants de type ETBE et MTBE

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    Traitement biologique in situ au sein d'un aquifère de polluants de type ETBE et MTBE Yves Benoit Villeurbanne (6) CNRS, UMR5557, Ecologie Microbienne ­ 69100 Villeurbanne Résumé Le MtBE et l' EtBE sont des : Traçabilité, Innocuité, Efficacité: Application aux polluants pétroliers type MTBE, ETBE), financé par le pôle

  11. REQUEST BY EATON CORPORATION FOR AN ADVANCE WAIVER OF DOMESTIC...

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

    DOE CONTRACT NO. DE-AC05-840R21400; DOE WAIVER DOCKET W(A)-94-011 ORO-578 The Eaton Corporation (Eaton) has made a timely request for an advance waiver to worldwide...

  12. REQUEST BY EATON CORPORATION FOR ADVANCE WAIVER OF DOMESTIC AND...

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

    AND OPERATING CONTRACT NO. DE-AC05-840R21400; DOE WAIVER DOCKET W(A)-93-003 0RO-548 Eaton Corporation (Eaton) has made a timely request for an advance waiver to worldwide...

  13. One multivariable controller increased capacity of an Oleflex{trademark}/MTBE complex

    SciTech Connect (OSTI)

    Robertson, D.; Peterson, T.J.; O`Connor, D. [Dynamic Matrix Control Corp., Houston, TX (United States); Adams, V.; Payne, D. [Valero Refining Co., Corpus Christi, TX (United States)

    1996-12-01T23:59:59.000Z

    Capacity increased by more than 4.6% when one dynamic matrix controller began operating in Valero Refining Company`s MTBE production complex in Corpus Christi, Texas. This was on a plant that was already running well above design capacity due to process changes previously made on the plant. A single controller was developed to cover an Oleflex{trademark} isobutane dehydrogenation unit and an MTBe reaction and fractionation plant with the intermediate isobutylene surge drum. The overall benefit is realized by a comprehensive constrained multivariable predictive controller which properly handles all sets of limits experienced by the complex, whether limited by the front-end Oleflex{trademark} or back-end MTBE unit. The controller has 20 manipulated, 6 disturbance and 44 controlled variables, and covers widely varying dynamics with settling times ranging from twenty minutes to six hours. The controller executes each minute with a six hour time horizon. A unique achievement is intelligent handling of the surge drum level by the controller for higher average daily capacity of the complex as a whole. The Oleflex{trademark} often operates at simultaneous limits on reactor effluent compressor capacity, cold box temperature and hydrogen/hydrocarbon ratio and the MTBE at impurity in butene column overhead as well as impurity in MTBE product.

  14. Relationship between MTBE-blended gasoline properties and warm-up driveability

    SciTech Connect (OSTI)

    Suzawa, Takumi; Yamaguchi, Kazunori; Kashiwabara, Kimito [Mitsubishi Motors Corp., Tokyo (Japan); Fujisawa, Norihiro; Matsubara, Michiro

    1995-12-31T23:59:59.000Z

    The relationship between MBE-blended gasoline properties and warm-up driveability is investigated by focusing on the transient combustion air-fuel ratio that strongly relates to the combustion state of the engine. As a result, although warm-up driveability of MTBE-free gasoline has a high correlation with 50% distillation temperature (T50) and a high correlation with 100 C distillation volume (E100), the correlation is found to be low when blended with MTBE. Various formulas that improve correlation with peak excess air ratio ({lambda}) by correcting T50 and E100 for the amount of MTBE blended are examined. The formula for which the highest determination coefficient is obtained is proposed as a new driveability index (DI) that can also be applied to MTBE-blended gasoline. In addition, the effect on driveability by gasoline base materials using this new DI also is investigated. The results indicate that the new DI worsen when heavy reformate containing large amounts of aromatics or MTBE, an oxygen-containing compound, is used for the octane improver, leaving the balance of the volatility out of consideration.

  15. Whole-Genome Analysis of Methyl tert-Butyl Ether-Degrading Beta-Proteobacterium Methylibium petroleiphilum PM1

    E-Print Network [OSTI]

    2007-01-01T23:59:59.000Z

    D. J. Slomczynski. 2003. BTEX/MTBE bioremediation: BionetsScow, and L. Alvarez-Cohen. MTBE and benzene biodegradationinteractions in BTEX and MTBE mixtures by an MTBE-degrading

  16. Proceedings of the National Groundwater National Ground Water Association Southwest focused ground water conference: Discussing the issue of MTBE and perchlorate in the ground water, Anaheim, CA, June 3-4, pp:87-90.

    E-Print Network [OSTI]

    ground water conference: Discussing the issue of MTBE and perchlorate in the ground water, Anaheim, CA

  17. Whole-genorne analysis of the methyl tert-butyl ether-degrading beta-proteobacterium Methylibium petroleiphilum PM1

    SciTech Connect (OSTI)

    Kane, Staci R. [Lawrence Livermore National Laboratory (LLNL); Chakicherla, Anu Y. [Lawrence Livermore National Laboratory (LLNL); Chain, Patrick S. G. [Lawrence Livermore National Laboratory (LLNL); Schmidt, Radomir [University of California, Davis; Shin, M [U.S. Department of Energy, Joint Genome Institute; Legler, Tina C. [Lawrence Livermore National Laboratory (LLNL); Scow, Kate M. [University of California, Davis; Larimer, Frank W [ORNL; Lucas, Susan [Joint Genome Institute, Walnut Creek, California; Richardson, P M [U.S. Department of Energy, Joint Genome Institute; Hristova, Krassimira R. [University of California, Davis

    2007-03-01T23:59:59.000Z

    Methylibium petroleiphilum PM1 is a methylotroph distinguished by its ability to completely metabolize the fuel oxygenate methyl tert-butyl ether (MTBE). Strain PM1 also degrades aromatic (benzene, toluene, and xylene) and straight-chain (C, to C,,) hydrocarbons present in petroleum products. Whole-genome analysis of PM1 revealed an similar to 4-Mb circular chromosome and an similar to 600-kb megaplasmid, containing 3,831 and 646 genes, respectively. Aromatic hydrocarbon and alkane degradation, metal resistance, and methylotrophy are encoded on the chromosome. The megaplasmid contains an unusual t-RNA island, numerous insertion sequences, and large repeated elements, including a 40-kb region also present on the chromosome and a 29-kb tandem repeat encoding phosphonate transport and cobalamin biosynthesis. The megaplasmid also codes for alkane degradation and was shown to play an essential role in MTBE degradation through plasmid-curing experiments. Discrepancies between the insertion sequence element distribution patterns, the distributions of best BLASTP hits among major phylogenetic groups, and the G+C contents of the chromosome (69.2%) and plasmid (66%), together with comparative genome hybridization experiments, suggest that the plasmid was recently acquired and apparently carries the genetic information responsible for PM1's ability to degrade MTBE. Comparative genomic hybridization analysis with two PM1-like MTBE-degrading environmental isolates (similar to 99% identical 16S rRNA gene sequences) showed that the plasmid was highly conserved (ca. 99% identical), whereas the chromosomes were too diverse to conduct resequencing analysis. PM1's genome sequence provides a foundation for investigating MTBE biodegradation and exploring the genetic regulation of multiple biodegradation pathways in M. petroleiphilum and other MTBE-degrading beta-proteobacteria.

  18. Class Patent Waiver W(C)2012-005 | Department of Energy

    Office of Environmental Management (EM)

    Waiver W(C)2012-005 More Documents & Publications Class Patent Waiver W(C)2010-007 Class Patent Waiver W(C)2009-001 WC2004004CLASSWAIVERFORNATIONALHYDROGENSTORAGEPROJE...

  19. Advance Patent Waiver W(A)2012-003 | Department of Energy

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

    Waiver W(A)2012-003 More Documents & Publications Advance Patent Waiver W(A)2013-019 Class Patent Waiver W(C)2012-003 WA02048EATONCORPORATIONWaviverofPatentRightsUnderA...

  20. Isobaric vapor-liquid equilibria in the systems methyl 1,1-dimethylethyl ether + hexane and + heptane

    SciTech Connect (OSTI)

    Wisniak, J.; Magen, E.; Shachar, M.; Zeroni, I.; Segura, H. [Ben-Gurion Univ. of the Negev, Beer-Sheva (Israel). Dept. of Chemical Engineering] [Ben-Gurion Univ. of the Negev, Beer-Sheva (Israel). Dept. of Chemical Engineering; Reich, R. [Univ. de Concepcion (Chile). Dept. of Chemical Engineering] [Univ. de Concepcion (Chile). Dept. of Chemical Engineering

    1997-03-01T23:59:59.000Z

    The vapor-liquid equilibrium at 94 kPa has been determined for the binary systems of methyl 1,1-dimethylethyl ether (MTBE) with hexane and with heptane. Both systems deviate slightly from ideal behavior, can be described as regular solutions, and do not present an azeotrope. The activity coefficients and boiling point of the solutions were correlated with its composition by the Redlich-Kister, Wohl, Wilson, UNIQUAC, NRTL, and Wisniak-Tamir equations.

  1. WC_2000_003_CLASS_WAIVER_FOR_BWXT_UNDER_A_MANAGEMENT_AND_OPE...

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

    NDERAMANAGEMENTANDOPE.pdf More Documents & Publications ClassWaiverWC-2000-003.pdf WC2000004CLASSWAIVERMadeinthePerformanceofCRADAby.pdf ClassWaiverWC-2000-004...

  2. 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

  3. 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

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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

  9. 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

  10. 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.

  11. 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.

  12. 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

  13. 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.

  14. 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.

  15. 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.

  16. 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

  17. 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.

  18. Advance Patent Waiver W(A)2010-031

    Broader source: Energy.gov [DOE]

    This is a request by CHRYSLER CORPORATION for a DOE waiver of domestic and foreign patent rights under agreement DE-EE0003347

  19. 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

  20. 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.

  1. 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.

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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.

  7. 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

  8. 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.

  9. 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.

  10. 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.

  11. 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.

  12. 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

  13. Advance Patent Waiver W(A)2010-026

    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-EE0002883

  14. 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

  15. 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.

  16. 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

  17. 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

  18. 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

  19. 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.

  20. 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

  1. 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.

  2. 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.

  3. 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.

  4. Advance Patent Waiver W(A)2006-029

    Broader source: Energy.gov [DOE]

    This is a request by GENSCAPE, INC. for a DOE waiver of domestic and foreign patent rights under agreement DE-FC26-06NT42795

  5. 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

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  11. Advance Patent Waiver W(A)2007-020

    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-FC26-06NT42950

  12. 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

  13. 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.

  14. 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

  15. 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.

  16. 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.

  17. 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

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

    Broader source: Energy.gov [DOE]

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

  19. 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.

  20. 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.

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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

  7. 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.

  8. 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

  9. 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

  10. 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.

  11. 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

  12. 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.

  13. 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

  14. 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

  15. 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

  16. 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.

  17. 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.

  18. 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

  19. 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.

  20. 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

  1. 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

  2. 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.

  3. 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

  4. 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

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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.

  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. 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.

  13. 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.

  14. 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

  15. 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

  16. 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.

  17. 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.

  18. 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

  19. 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.

  20. STATEMENT OF CONSIDERATIONS CLASS WAIVER OF GOVERNMENT PATENT...

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

    GOVERNMENT PATENT RIGHTS FOR PROPRIETARY USERS OF FACILITIES ESTABLISHED UNDER THE PHOTOVOLTAIC MANUFACTURING INITIATIVE (DE-FOA-0000259) DOE WAIVER NO. W(C) 2011-004 The...

  1. 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

  2. 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

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

    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-FC26-08NT0005310

  4. 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

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

    Broader source: Energy.gov [DOE]

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

  6. 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.

  7. 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.

  8. 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.

  9. 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

  10. 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

  11. 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.

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

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

    inventions made by its employees under its Prime Contract. STATEMENT OF CONSIDERATIONS CRADA INVENTIONS Page 2 Class Advance Waiver to Participants' Inventions The scope of this...

  13. 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

  14. 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

  15. Advance Patent Waiver W(A)2005-051

    Broader source: Energy.gov [DOE]

    This is a request by SOUTHERN COMPANY SERVICE for a DOE waiver of domestic and foreign patent rights under agreement DE-FC02-05CH11327.

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

    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-FC26-06NT42947

  17. Advance Patent Waiver W(A)2005-032

    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 DE-FC36-02AL67624.

  18. 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

  19. 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.

  20. 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

  1. 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.

  2. 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.

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

    Broader source: Energy.gov [DOE]

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

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

    Broader source: Energy.gov [DOE]

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

  5. 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.

  6. 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.

  7. Exposure to methyl tert-butyl ether, benzene, and total hydrocarbons at the Singapore-Malaysia causeway immigration checkpoint

    SciTech Connect (OSTI)

    Tan, C.; Ong, H.Y.; Kok, P.W. [and others

    1996-12-31T23:59:59.000Z

    The primary aim of this study was to determine the extent and levels of exposure to volatile organic compounds (VOCs) from automobile emissions in a group of immigration officers at a busy cross-border checkpoint. A majority (80%) of the workers monitored were exposed to benzene at levels between 0.01 and 0.5 ppm, with only 1.2% exceeding the current Occupational Safety and Health Administration occupational exposure limit of 1 ppm. The geometric mean (GM) concentrations of 8-hr time-weighted average exposure were 0.03 ppm, 0.9 ppm, and 2.46 ppm for methyl-tert-butyl ether (MTBE), benzene, and total hydrocarbons (THC), respectively. The highest time-weighted average concentrations measured were 1.05 ppm for MTBE, 2.01 ppm for benzene, and 34 ppm for THC. It was found that motorbikes emitted a more significant amount of pollutants compared with motor cars. On average, officers at the motorcycle booths were exposed to four to five times higher levels of VOCs (GMs of 0.07 ppm, 0.23 ppm, and 4.7 ppm for MTBE, benzene, and THC) than their counterparts at the motor car booths (GMs of 0.01 ppm, 0.05 ppm, and 1.5 ppm). The airborne concentrations of all three pollutants correlated with the flow of vehicle traffic. Close correlations were also noted for the concentrations in ambient air for the three pollutants measured. Benzene and MTBE had a correlation coefficient of 0.97. The overall findings showed that the concentrations of various VOCs were closely related to the traffic density, suggesting that they were from a common source, such as exhaust emissions from the vehicles. The results also indicated that although benzene, MTBE, and THC are known to be volatile, a significant amount could still be detected in the ambient environment, thus contributing to our exposure to these compounds. 4 refs., 6 figs.

  8. Gas phase synthesis of MTBE from methanol and isobutene over dealuminated zeolites

    SciTech Connect (OSTI)

    Collignon, F.; Mariani, M.; Moreno, S.; Remy, M.; Poncelet, G. [Universite Catholique de Louvain (Belgium)] [Universite Catholique de Louvain (Belgium)

    1997-02-01T23:59:59.000Z

    Gas phase synthesis of MTBE from methanol and isobutene has been investigated over different zeolites. It is shown that bulk Si/Al ratio has a marked influence on the formation of MTBE. H-beta zeolite was found to be as active as acid Amberlyst-15 (reference catalyst), and noticeably superior to non- and dealuminated forms of H-Y, H-ZSM-5, zeolite omega, and H-mordenites. Screening test results obtained over other catalysts (SAPOs and pillared clays) are briefly commented. The contribution of the external surface of the zeolites to the reaction is discussed. In the case of H-Y zeolites, it is shown that extra framework Al species ({sup 27}Al NMR signal at 30 ppm) have a detrimental effect on the reaction. 64 refs., 12 figs., 3 tabs.

  9. Rates and products of degradation for MTBE and other oxygenate fuel additives in the subsurface environment

    SciTech Connect (OSTI)

    Tratnyek, P.G.; Church, C.D.; Pankow, J.F. [Oregon Graduate Inst., Portland, OR (United States). Dept. of Environmental Science and Engineering

    1995-12-31T23:59:59.000Z

    The recent realization that oxygenated fuel additives such as MTBE are becoming widely distributed groundwater contaminants has created a sudden and pressing demand for data on the processes that control their environmental fate. Explaining and predicting the subsequent environmental fate of these compounds is going to require extrapolations over long time frames that will be very sensitive to the quality of input data on each compound. To provide such data, they have initiated a systematic study of the pathways and kinetics of fuel oxygenate degradation under subsurface conditions. Batch experiments in simplified model systems are being performed to isolate specific processes that may contribute to MTBE degradation. A variety of degradation pathways can be envisioned that lead to t-butyl alcohol (TBA) as the primary or secondary product. However, experiments to date with a facultative iron reducing bacteria showed no evidence for TBA formation. Continuing experiments include mixed cultures from a range of aquifer materials representative of NAWQA study sites.

  10. Active Duty Military Tuition Waiver UNIVERSITY OF NEW MEXICO

    E-Print Network [OSTI]

    New Mexico, University of

    Active Duty Military Tuition Waiver UNIVERSITY OF NEW MEXICO SEMESTER: __________ YEAR of the (DUTY STATION) State of New Mexico. This active duty assignment is for the period from _______________________________________________________ ORGANIZATION Return waiver to: The University of New Mexico Division of Enrollment Management Office

  11. LIDEM unit for the production of methyl tert-butyl ether from butanes

    SciTech Connect (OSTI)

    Rudin, M.G.; Zadvornov, M.A.

    1994-09-01T23:59:59.000Z

    One of the basic problems in the production of motor fuels is how to obtain high-octane unleaded gasolines that will meet today`s ecological requirements. The term {open_quotes}reformulated gasolines{close_quotes} has come into general use throughout the world to denote fuels with a certain chemical composition. These gasolines consist of preselected components; as shown by worldwide experience, they must include oxygen-containing compounds that are distinguished by high octane numbers and low reactivities. Standards in effect in the United States, Japan, and certain Western European countries require that automotive gasolines must contain at least 2-4% by weight of oxygen-containing compounds (calculated as oxygen). In the last 15 years, in order to meet these requirements, production has been set up in various countries for the manufacture of high-octane oxygen-containing components known as oxygenates. The most common of these is methyl tert-butyl ether (MTBE), obtained by etherification of isobutene by methanol. Process technology developed by this last organization was used as the basis for constructing a unit in the Nizhnekamskneftekhim Production Association and at the Mazheikyai Petroleum Refinery in Lithuania. MTBE production has been held back mainly by a shortage of isobutene, which is obtained mainly from butane-butene cuts produced in cat crackers. In order to alleviate this shortage, it has been proposed that MTBE should be obtained from saturated C{sub 4} hydrocarbons that are recovered in processing oilfield associated gas, and also in the refinery from primary distillation units, catalytic reformers, and hydrocrackers. A working design was developed in 1991-1992 by Lengiproneftekhim for a basically new combination unit designed for the processing of saturated C{sub 4} hydrocarbons, which has been termed the LIDEM unit (Leningrad - isomerization - dehydrogenation - MTBE).

  12. Stratospheric ozone, global warming, and the principle of unintended consequences - an ongoing science and policy story

    E-Print Network [OSTI]

    2013-01-01T23:59:59.000Z

    as methyl-tert-butyl ether (MTBE), lubricating oil and itsthe environment. Use of the MTBE additive in gasoline wasof gasoline laced with MTBE into groundwater resulted in

  13. Energy Efficiency Improvement and Cost Saving Opportunities for the Petrochemical Industry - An ENERGY STAR(R) Guide for Energy and Plant Managers

    E-Print Network [OSTI]

    Neelis, Maarten

    2008-01-01T23:59:59.000Z

    Ethylene dichloride 1 MTBE 2 Vinylchloride 3 Ethylbenzene 1Methyl- Tertiary-Butyl-Ether (MTBE) or Ethyl-Tertiary-Butyl-Styrene Vinylchloride MTBE Benzene, Toluene, Xylene Acetone

  14. Cometabolic bioremediation

    E-Print Network [OSTI]

    Hazen, Terry C.

    2010-01-01T23:59:59.000Z

    Intrinsic bioremediation of MTBE-contaminated groundwater atcontaminants, e.g. PCE, TCE, MTBE, TNT, dioxane, atrazine,Methyl tert-butyl ether (MTBE) has also been remediated

  15. Synthesis of octane enhancers during slurry-phase Fischer-Tropsch. [801Methyl tert-butyl ether

    SciTech Connect (OSTI)

    Marcelin, G.

    1992-06-24T23:59:59.000Z

    The objective of this project is to investigate three possible routes to the formation of ethers, in particular methyl tert-butyl ether (MTBE), during slurry phase Fischer-Tropsch reaction. The three reaction schemes to be investigated are: (1) Addition of isobutylene during the formation of methanol and/or higher alcohols directly from CO and H{sub 2} during slurry-phase Fischer-Tropsch. (2) Addition of isobutylene to FT liquid products including alcohols in a slurry-phase reactor containing an MTBE or other acid catalyst. (3) Addition of methanol to slurry phase FT synthesis making iso-olefins. During the sixth quarter we completed the construction of the slurry bubble column reactor (SBCR), conducted initial shake-down experiments in a cold-flow mode, and finalized the selection process of the acid catalysts for conversion of syngas-produced alcohols and isobutylene to MTBE (scheme 2). Tasks 3, 4, and 5 are awaiting complete implementation of the SBCR system.

  16. Advance Patent Waiver W(A)2010-028 | Department of Energy

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

    W(A)2010-028 More Documents & Publications Advance Patent Waiver W(A)2009-028 Novel Materials for High Efficiency Direct Methanol Fuel Cells Advance Patent Waiver W(A)2008-019...

  17. Advance Patent Waiver W(A)2009-039 | Department of Energy

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

    Advance Patent Waiver W(A)2010-007 Advance Patent Waiver W(A)2012-034 Stabilized Lithium Metal Powder, Enabling Material and Revolutionary Technology for High Energy Li-ion...

  18. Advance Patent Waiver W(A)2005-006 | Department of Energy

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

    W(A)2005-006 More Documents & Publications Advance Patent Waiver W(A)2008-022 WA04079PRAXAIRINCWaiverofPatentRightsUnderaSubcon.pdf Advance Patent Waiver W(A)2011-063...

  19. Non-Availability Waivers | Department of Energy

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

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels DataDepartment of Energy Your Density Isn'tOrigin of Contamination in Many DevilsForumEnginesVacant Under SecretaryNon-Availability Waivers

  20. Treatment of methyl tert-butyl ether vapors in a biotrickling filters. 2. Analysis of the rate-limiting step and behavior under transient conditions

    SciTech Connect (OSTI)

    Fortin, N.Y.; Deshusses, M.A. [Univ. of California, Riverside, CA (United States). Dept. of Chemical and Environmental Engineering] [Univ. of California, Riverside, CA (United States). Dept. of Chemical and Environmental Engineering

    1999-09-01T23:59:59.000Z

    Detailed experiments were performed with gas phase biotrickling filters treating vapors of methyl tert-butyl ether (MTBE), a gasoline additive of great environmental concern. A particular emphasis was placed on the analysis of the rate-limiting step, and it was found that the process was mostly limited by the biological reaction rather than by mass transfer. Further experiments involved the study of the dynamic behavior of the biotrickling filters under simulated field conditions. In all cases, the biotrickling filters adapted rapidly to the new conditions, and new steady states were obtained within hours. The relevance of the results and the implications as far as implementation of biotrickling filters for field MTBE treatment are discussed.

  1. 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.

  2. 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.

  3. 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.

  4. STATEMENT OF CONSIDERATIONS Advance Test Reactor Class Waiver

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

    Advance Test Reactor Class Waiver W(C)-2008-004 The Advanced Test Reactor (A TR) is a pressurized water test reactor at the Idaho National Laboratory (INL) that operates at low...

  5. 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.

  6. 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.

  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. 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.

  9. 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

  10. 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.

  11. 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.

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

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

    Test Site was managed and operated by two additional prime contractors, REECO and Raytheon, each of which had its own prime contract. EG&G was granted a class waiver...

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

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

    Test Site was managed and operated by two additional prime contractors, REECO and Raytheon, each of which had its own prime contract. EG&G was granted a Class Waiver...

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

    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-FC26-08NT01911

  15. STATEMENT OF CONSIDERATIONS PETITION FOR ADVANCE WAIVER OF PATENT...

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

    PRAXAIR INC. ("PRAXAIR") UNDER AGREEMENT NO. DE-FG36-08G018063 BETWEEN PRAXAIRAND DOE; W(A-2010-19; CH-1551 The Petitioner, PRAXAIR, has requested a waiver of domestic and certain...

  16. 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

  17. Advance Patent Waiver W(A)2005-025

    Broader source: Energy.gov [DOE]

    This is a request by G.E. NUCLEAR ENERGY for a DOE waiver of domestic and foreign patent rights under agreement DE-FC07-05ID14635

  18. 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

  19. 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.

  20. 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

  1. Advance Patent Waiver W(A)2005-060

    Broader source: Energy.gov [DOE]

    This is a request by SHELL SOLAR INDUSTRIES, LP for a DOE waiver of domestic and foreign patent rights under agreement DE-AC36-98GO10337.

  2. STATEMENT OF CONSIDERATIONS ADVANCE WAIVER OF PATENT RIGHTS TO...

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

    0 STATEMENT OF CONSIDERATIONS ADVANCE WAIVER OF PATENT RIGHTS TO HONEYWELL TURBO TECHNOLOGIES (HTT) UNDER DOE PRIME CONTRACT NO. DE-DE-FC26- 06NT42873 FOR "ADVANCED TURBO-CHARGING...

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

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

    to Designated Non-Proprietary User facilities at all DOE facilities funded by any DOE program. Therefore, the 1983 Non-Proprietary User Class Waiver is superseded by this new...

  4. VOL. 32, No.4 UNL WATER CENTER AUGUST 2000 New Method For Detecting Trace Amounts of MTBE

    E-Print Network [OSTI]

    Nebraska-Lincoln, University of

    of MTBE and Ethanol at Heart ofUNL Contamination Research with ethanol, which also reduces harmful vehicle "Although ethanol is the same alcohol consumed in contaminate the water we drink. But they can be diffi have cern that ethanol could negatively impact the ability of developed a method for detecting minute

  5. The social costs of an MTBE ban in California (Long version)

    E-Print Network [OSTI]

    Rausser, Gordon C.; Adams, Gregory D.; Montgomery, W. David; Smith, Anne E.

    2002-01-01T23:59:59.000Z

    ethyl tertiary-butyl ether (ETBE) or tertiary amyl methylOther oxygenates, such as ETBE and TAME exist. However,

  6. Emissions of volatile organic compounds inferred from airborne flux measurements over a megacity

    E-Print Network [OSTI]

    Karl, T.; Apel, E.; Hodzic, A.; Riemer, D. D; Blake, D. R; Wiedinmyer, C.

    2009-01-01T23:59:59.000Z

    methyl-tertiary-butyl- ether (MTBE) and the biomass burningfrom all source categories. MTBE is a gasoline additive andwith the fuel tracer MTBE (e.g. 0.82 for MTBE/benzene).

  7. Sonolytic destruction of methyl tert-butyl ether by ultrasonic irradiation: The role of O{sub 3}, H{sub 2}O{sub 2}, frequency, and power density

    SciTech Connect (OSTI)

    Kang, J.W.; Hung, H.M.; Lin, A.; Hoffmann, M.R. [California Inst. of Tech., Pasadena, CA (United States). W.M. Keck Labs.] [California Inst. of Tech., Pasadena, CA (United States). W.M. Keck Labs.

    1999-09-15T23:59:59.000Z

    The kinetics of degradation of methyl tert-butyl ether (MTBE) by ultrasonic irradiation in the presence of ozone as functions of applied frequencies and applied power are investigated. Experiments are performed over the frequency range of 205--1,078 kHz. The higher overall reaction rates are observed at 358 and 618 kHz and then at 205 and 1,078 kHz. The observed pseudo-first-order rate constant, k{sub 0}, for MTBE degradation increases with increasing power density up to 250 W L{sup {minus}1}. A linear dependence of the first-order rate constant, k{sub O{sub 3}}, for the simultaneous degradation of O{sub 3} on power density is also observed. Naturally occurring organic matter (NOM) is shown to have a negligible effect on observed reaction rates.

  8. Massachusetts Institute of Technology Affiliate Health Insurance Waiver Form

    E-Print Network [OSTI]

    Polz, Martin

    Massachusetts Institute of Technology Affiliate Health Insurance Waiver Form Affiliate's last name A deductible not to exceed $500 per accident or illness Please carefully review the standards listed below for: mental and nervous conditions (60 inpatient days per year); alcohol and drug abuse; and maternity

  9. Potential Supply Impacts of Removal of 1-Pound RVP Waiver

    E-Print Network [OSTI]

    Patzek, Tadeusz W.

    trends, and current laws and regulations. The EIA's Annual Energy Outlook 2002 (AEO2002) is usedPotential Supply Impacts of Removal of 1-Pound RVP Waiver September 2002 #12;ii Energy Information by the Office of Oil and Gas of the Energy Information Administration. General questions concerning the report

  10. University of Oklahoma Norman Campus WAIVER and RELEASE of LIABILITY

    E-Print Network [OSTI]

    Oklahoma, University of

    University of Oklahoma Norman Campus WAIVER and RELEASE of LIABILITY This is a legal and binding. The University of Oklahoma is a state educational institution. References to the University of Oklahoma include: _______________________________________________ _______________________________________________ _______________________________________________ I understand that the University of Oklahoma is not an agent of and has no responsibility for any

  11. Class_Waiver_W_C-2001-002.pdf | Department of Energy

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

    Documents & Publications WC2001002CLASSWAIVERToFACULTYMEMBERSOFHISTORICALLY.pdf WC1990014CLASSADVANCEWAIVERofUSandForeignRightsfo.pdf ClassWaiverWC-2000-002...

  12. Class_Waiver_W_C-2000-002.pdf | Department of Energy

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

    More Documents & Publications ClassWaiverWC-2001-002.pdf Subcontractor Rights Under CRADAs and WFO Agreements WC1990012CLASSWAIVERofPatentRightsinInventionsMade.pdf...

  13. WA_1994_017_GOLDEN_TECHNOLOGIES_COMPANY_Waiver_of_Domestic_a...

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

    for An Advance Waiver of Domestic and Foreign Rights. January 10, 1995 WA1994011EATONCORPORATIONWaiverofDomesticandForeign.pdf WA1994014GOLDENTECHNOLOGIESCOMPA...

  14. WA_1993_022_NORTON_COMPANY_Waiver_of_Domestic_and_Foreign_Ri...

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

    Golden Technologies Company, Inc. Request for An Advance Waiver of Domestic and Foreign Rights. January 10, 1995 WA1994011EATONCORPORATIONWaiverofDomesticandForeign...

  15. WC_1999_006_CLASS_WAIVER_FOR_BECHTEL_RESEARCH_AND_CO-OP_AGRE...

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

    Documents & Publications WC1999005CLASSWAIVERBECHTELBWXTIDAHOLLCManagement.pdf WC2000004CLASSWAIVERMadeinthePerformanceofCRADAby.pdf ClassWaiverWC-2000-004...

  16. Class_Waiver_W_C-2000-003.pdf | Department of Energy

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

    Documents & Publications WC2000003CLASSWAIVERFORBWXTUNDERAMANAGEMENTANDOPE.pdf WC2000004CLASSWAIVERMadeinthePerformanceofCRADAby.pdf ClassWaiverWC-2000-004...

  17. Class_Waiver_W_C-2000-004.pdf | Department of Energy

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

    More Documents & Publications WC2000004CLASSWAIVERMadeinthePerformanceofCRADAby.pdf ClassWaiverWC-2000-003.pdf WC2000003CLASSWAIVERFORBWXTUNDERAMANAGEM...

  18. Treatment of Methyl tert-Butyl Ether Contaminated Water Using a Dense

    E-Print Network [OSTI]

    Dandy, David

    -butyl ether (MTBE) in a dense medium plasma (DMP) reactor utilizing gas chromatog- raphy-massspectrometryandgaschromatography-thermal conductivity techniques. A rate law is developed for the removal of MTBE from an aqueous solution in the DMP. The oxidation products from the treatment of MTBE-contaminated water in the DMP reactor were found

  19. he increasing frequency of detection of the widely used gasoline additive methyl tert-

    E-Print Network [OSTI]

    ether (MTBE) in both ground and sur- face waters is receiving much attention from the media and 10% of community drinking water sup- plies in high MTBE use areas show at least detectable concentrations of MTBE, and about 1% of those sys- tems are characterized by levels of this compound

  20. Pyrolysis of Organic Molecules Relevant to Combustion as Monitored by Photoionization Time-of-Flight Mass Spectrometry

    E-Print Network [OSTI]

    Weber, Kevin Howard

    2010-01-01T23:59:59.000Z

    is observed, which is similar to MTBE in this system whichisobutene formed from MTBE, is found to occur. REFERENCES [methyl tert-butyl ether (MTBE) and tert-amyl methyl ether (

  1. Life-cycle Environmental Inventory of Passenger Transportation in the United States

    E-Print Network [OSTI]

    Chester, Mikhail V

    2008-01-01T23:59:59.000Z

    Methyltert?ButylEther(MTBE);http://www.atsdr.cdc.gov/MethylTertiaryButyl Ether (MTBE), which was easilyaccountingwasnotperformedonMTBEandtheresult of

  2. REV 8.22.12 ACKNOWLEDGEMENT OF RISK AND WAIVER OF LIABILITY

    E-Print Network [OSTI]

    Tullos, Desiree

    REV 8.22.12 ACKNOWLEDGEMENT OF RISK AND WAIVER OF LIABILITY Event Name: Event Date: Event Time: Team/Club, etc. (if applicable): Read this Acknowledgement of Risk and Waiver of Liability carefully. I acknowledge that participation in this ACTIVITY has the following non-exhaustive list

  3. University of Idaho, SRC Climbing Center Acknowledgement of Risk and Waiver of Liability

    E-Print Network [OSTI]

    Waits, Lisette

    University of Idaho, SRC Climbing Center Acknowledgement of Risk and Waiver of Liability Signatures)Emergency contact: PHONE: CELL: Acknowledgement of Risk and Waiver of Liability Participant, and parent(s) / guardians of participant if participant is under 18 years of age, must read this Acknowledgement of Risk

  4. (distillation) (Le Chatelier

    E-Print Network [OSTI]

    Hong, Deog Ki

    acetate(methyl-, ethyl-, butyl-) , methanol isobutene MTBE , ethanol isobutene ETBE , methanol 2-methyl-1% MTBE 3 DMC . 2% 1990 MTBE 1999 3 2002 MTBE . [ 1-1 ] Phosgene process polycarbonate(PC) 50/ . DMC DMC MTBE / . ( : Amoco, "Review of DMC Manufacture and its

  5. Patent Waivers Approved Before 2003 | Department of Energy

    Energy Savers [EERE]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are being directed offOCHCO2:Introduction toManagementOPAM5Parabolic Trough Parabolic Trough DOEPatent Waivers Approved

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

    Energy Savers [EERE]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are being directed offOCHCO2:Introduction toManagement ofConverDyn NOPR ConverDyn NOPRNSRCC(A)WAIVER.pdf

  7. Multiple Objective Stormwater Management For the Coliseum Complex

    E-Print Network [OSTI]

    Jones, Jesse; Kraai, Rachel

    2009-01-01T23:59:59.000Z

    methyl tertiary butyl ether (MTBE) remain in the soil around5.2 ppb xylenes, and 160 ppb MTBE remain in the groundwater

  8. Effects of water chemistry on NF/RO membrane structure and performance

    E-Print Network [OSTI]

    Mo, Yibing

    2013-01-01T23:59:59.000Z

    methyl tert-butyl ether (MTBE), benzene, ethylbenzene,TCE** Industrial C 2 HCl 3 MTBE** [48] Industrial C 5 H 12 O

  9. Request for Waiver to Hire a Non-Student U of M Job Center

    E-Print Network [OSTI]

    Amin, S. Massoud

    = Request for Waiver to Hire a Non-Student U of M Job Center Office of Human Resources University: __________________________________________________________________________ __________________________________________________________________________________________ __________________________________________________________________________________________ __________________________________________________________________________________________ __________________________________________________________________________________________ U of M Job Center Representative: Date: The University of Minnesota is an equal opportunity educator

  10. WA_00_013_GENECOR_INTERNATIONAL_Waiver_of_US_Competitiveness...

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

    WaiverofUSCompetitiveness.pdf More Documents & Publications U.S. Biofuels Industry: Mind the Gap Advance Patent Waiver W(A)2008-045 WA01008NOVOZYMEBIOTECHWaiverofDomesti...

  11. Advance Patent Waiver W(A)2010-007 | Department of Energy

    Office of Environmental Management (EM)

    0-007 Advance Patent Waiver W(A)2010-007 This document waives certain patent rights the Department of Energy (DOE) has to inventions conceived or first actually reduced to practice...

  12. REQUEST BY PRAXAIR, INC.(PRAXAIR) FOR AN ADVANCE WAIVER OF DOMESTIC...

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

    PRAXAIR, INC.(PRAXAIR) FOR AN ADVANCE WAIVER OF DOMESTIC AND FOREIGN PATENT RIGHTS TO INVENTIONS MADE UNDER CONTRACT NO. DE-FC26-00NT41027 ENTITLED "NOVEL REACTOR FOR THE...

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

    SciTech Connect (OSTI)

    Stringfellow, William T.; Oh, Kuen-Chan

    2005-02-01T23:59:59.000Z

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

  14. Impacts of Ethanol on Anaerobic Production of Tert-Butyl Alcohol (TBA) from Methyl Tert-Butyl Ether (MTBE) in Groundwater

    E-Print Network [OSTI]

    Scow, K M; MacKay, Douglas

    2008-01-01T23:59:59.000Z

    field site is located at the Vandenberg Air Force Base at a site where a leaking underground storage

  15. A Low-Carbon Fuel Standard for California Part 1: Technical Analysis

    E-Print Network [OSTI]

    2007-01-01T23:59:59.000Z

    methyl-tertiary butyl ether (MTBE), from gasoline by 2004.MTBE was used to meet a requirement for gasoline to containbeginning in 2002, replacing MTBE with ethanol. According to

  16. The Scientific Basis for the Regulation of Nanoparticles: Challenging Paracelsus and Pare

    E-Print Network [OSTI]

    Goldstein, Bernard D.

    2010-01-01T23:59:59.000Z

    NANOTECHNOILOGY 402 (2007). 20. MTBE unquestionably causesTertiary-Butyl Ether (MTBE)-a Gasoline Additive-CausesMethyl Tertiary-butyl Ether (MTBE) in CD-I Mice and F-344

  17. Chemical evolution of volatile organic compounds in the outflow of the Mexico City Metropolitan area

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    Methanol Ethanol Acetone MEK MTBE CO Methane UCI UCI TOGA/methyl tertiary butyl ether (MTBE), and toluene all ratioedthe observed decay. For MTBE, also a species that is not

  18. Soil type, crop and irrigation technique affect nitrogen leaching to groundwater

    E-Print Network [OSTI]

    Letey, John; Vaughan, Peter

    2013-01-01T23:59:59.000Z

    water contamination with MTBE (methyl tertiary-butyl ether,that areas vulnerable to MTBE are also vulner- able tothat affect the movement of MTBE. If only a small amount of

  19. Measurements of volatile organic compounds at a suburban ground site (T1) in Mexico City during the MILAGRO 2006 campaign: measurement comparison, emission ratios, and source attribution

    E-Print Network [OSTI]

    2011-01-01T23:59:59.000Z

    methyl tert-butyl ether (MTBE) at 57 amu has been previouslyby a fragment of MTBE (62%) with minor contributions fromFortner and Knighton, 2008). MTBE also in- terfered (16%)

  20. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2-C10volatile organic compounds (VOCs), CO2, CH4, CO, NO, NO2, NOy, O3and SO2

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    methyl tertiary- butyl ether (MTBE) and its effect on plasmaand three VOCs (propyne, furan, MTBE) remained below their 3Ethanol Acetone MEK MAC MVK MTBE Furan CH 3 OH C 2 H 5 OH C

  1. A Low-Carbon Fuel Standard for California, Part 1: Technical Analysis

    E-Print Network [OSTI]

    Farrell, Alexander E.; Sperling, Dan

    2007-01-01T23:59:59.000Z

    methyl-tertiary butyl ether (MTBE), from gasoline by 2004.MTBE was used to meet a requirement for gasoline to containbeginning in 2002, replacing MTBE with ethanol. According to

  2. Finding the missing stratospheric Bry: a global modeling study of CHBr3 and CH2Br2

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    Methanol Ethanol Acetone MEK MTBE CO Methane UCI UCI TOGA/methyl tertiary butyl ether (MTBE), and toluene all ratioedthe observed decay. For MTBE, also a species that is not

  3. QUANTIFYING NON-POINT SOURCES OF VOLATILE ORGANIC COMPOUNDS IN STORMWATER FROM A PARKING LOT

    E-Print Network [OSTI]

    -butyl ether (MTBE) on urban particles indicates a site- specific interaction between MTBE and a particulate is a possible source only for the gasoline oxygenate methyl tert-butyl ether (MTBE). Lopes and Bender (1998

  4. Assessing the Effectiveness of California's Underground Storage Tank Annual Inspection Rate Requirements

    E-Print Network [OSTI]

    Cutter, W. Bowman

    2008-01-01T23:59:59.000Z

    Methyl Tert-Butyl Ether (MTBE), a gasoline additive. Thefor the lions share of MTBE contamination, as well asIn response to the MTBE crisis, California increased the

  5. Trichloroethene Removal From Waste Gases in Anaerobic Biotrickling Filters Through Reductive Dechlorination

    E-Print Network [OSTI]

    Popat, Sudeep Chandrakant

    2010-01-01T23:59:59.000Z

    methyl tert-butyl ether (MTBE) vapors into water was used.MTBE is highly soluble in water (dimensionless Henrysgas stream was laden with MTBE vapors (200-300 mg m -3 )

  6. Life-Cycle Water Impacts of U.S. Transportation Fuels

    E-Print Network [OSTI]

    Scown, Corinne Donahue

    2010-01-01T23:59:59.000Z

    Drinking Water: Methyl Tertiary Butyl Ether (MTBE).http://www.epa.gov/mtbe/water.htm (11/30/10), Chiu, Y. W. ;LCFS LCI LP LPG MED MRO MSF MTBE MWD MWDOC NAICS NERC NETL

  7. Measurement and Treatment of Nuisance Odors at Wastewater Treatment Plants

    E-Print Network [OSTI]

    Abraham, Samantha Margaret

    2014-01-01T23:59:59.000Z

    in the presence of MTBE, ETBE and TAME. Chemosphere 85, 616-Xanthomonas sp. MTBE/ETBE/TAME a Acinetobacter calcoaceticusMTBE= Methyl tert-Butyl Ether, ETBE= Ethyl tert-Butyl Ether,

  8. Whole-Genome Analysis of Methyl tert-Butyl Ether-Degrading Beta-Proteobacterium Methylibium petroleiphilum PM1

    E-Print Network [OSTI]

    2007-01-01T23:59:59.000Z

    2003. BTEX/MTBE bioremediation: Bionets containing Isolite,In Situ and On-site Bioremediation Symposium. Battellebacteria for use in bioremediation. FEMS Lett. 22. Dennis,

  9. Alternative Compliance: Guidelines for Preparing and Submitting a Waiver Request Application and Other Documentation Requirements (Book)

    SciTech Connect (OSTI)

    Not Available

    2010-11-01T23:59:59.000Z

    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.

  10. Alternative Compliance: Guidelines for Preparing and Submitting a Waiver Request Application and Other Documentation Requirements (Book)

    SciTech Connect (OSTI)

    Sears, T.

    2014-01-01T23:59:59.000Z

    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.

  11. Alternative Compliance: Guidelines for Preparing and Submitting a Waiver Request Application and Other Documentation Requirements

    SciTech Connect (OSTI)

    Not Available

    2013-03-01T23:59:59.000Z

    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.

  12. SPORT & RECREATION SERVICES-ICE HOCKEY INTRAMURALS RELEASE OF LIABILITY, WAIVER OF CLAIMS,

    E-Print Network [OSTI]

    Burg, Theresa

    of injury arising from falling and impacting against the floor or ice surface, walls or rink boardsSPORT & RECREATION SERVICES-ICE HOCKEY INTRAMURALS RELEASE OF LIABILITY, WAIVER OF CLAIMS #:______________________ TO: THE UNIVERSITY OF LETHBRIDGE (THE "UOFL"), THE ACTIVITY: The UofL plays host to Ice Hockey

  13. WAIVER OF RIGHT TO PRE-TERMINATION HEARING FOR CLASSIFIED STAFF ONLY

    E-Print Network [OSTI]

    Rhoads, James

    WAIVER OF RIGHT TO PRE-TERMINATION HEARING FOR CLASSIFIED STAFF ONLY Office of Human Resources Rev Discipline and SPP 1011 Involuntary Terminations, you are entitled to a pre-termination hearing prior to the effective date of termination stated in your Notice of Intent to Recommend Termination. The purpose

  14. BOWLING GREEN STATE UNIVERSITY LIABILITY RELEASE, WAIVER, DISCHARGE AND AGREEMENT NOT TO SUE

    E-Print Network [OSTI]

    Moore, Paul A.

    BOWLING GREEN STATE UNIVERSITY LIABILITY RELEASE, WAIVER, DISCHARGE AND AGREEMENT NOT TO SUE 1. I, forever discharge, and covenant not to sue the State of Ohio, Bowling Green State University, and its employment with Bowling Green State University. If I am a driver, driving my personal vehicle, I certify

  15. Alternative Compliance: Guidelines for Preparing and Submitting a Waiver Request Application and Other Documentation Requirements (Brochure)

    SciTech Connect (OSTI)

    Not Available

    2014-06-01T23:59:59.000Z

    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.

  16. Temperature-Dependent Photoelectron Spectroscopy of Methyl-Benzoate...

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

    Spectroscopy of Methyl-Benzoate Anions: Observation of Steric Effect in Ortho-Methyl Temperature-Dependent Photoelectron Spectroscopy of Methyl-Benzoate Anions: Observation of...

  17. Effect of Ethanol and Methyl-tert-Butyl Ether on Monoaromatic Hydrocarbon Biodegradation: Response Variability for Different Aquifer Materials Under Various Electron-Accepting Conditions

    SciTech Connect (OSTI)

    Ruiz-Aguilar, G L; Fernandez-Sanchez, J M; Kane, S R; Kim, D; Alvarez, P J

    2003-10-06T23:59:59.000Z

    Aquifer microcosms were used to determine how ethanol and methyl-tert-butyl ether (MtBE) affect monoaromatic hydrocarbon degradation under different electron-accepting conditions commonly found in contaminated sites experiencing natural attenuation. Response variability was investigated by using aquifer material from four sites with different exposure history. The lag phase prior to BTEX (benzene, toluene, ethylbenzene, and xylenes) and ethanol degradation was typically shorter in microcosms with previously contaminated aquifer material, although previous exposure did not always result in high degradation activity. Toluene was degraded in all aquifer materials and generally under a broader range of electron-accepting conditions compared to benzene, which was degraded only under aerobic conditions. MtBE was not degraded within 100 days under any condition, and it did not affect BTEX or ethanol degradation patterns. Ethanol was often degraded before BTEX compounds, and had a variable effect on BTEX degradation as a function of electron-accepting conditions and aquifer material source. An occasional enhancement of toluene degradation by ethanol occurred in denitrifying microcosms with unlimited nitrate; this may be attributable to the fortuitous growth of toluene-degrading bacteria during ethanol degradation. Nevertheless, experiments with flow-through aquifer columns showed that this beneficial effect could be eclipsed by an ethanol-driven depletion of electron acceptors, which significantly inhibited BTEX degradation and is probably the most important mechanism by which ethanol could hinder BTEX natural attenuation. A decrease in natural attenuation could increase the likelihood that BTEX compounds reach a receptor as well as the potential duration of exposure.

  18. Detailed chemical kinetic reaction mechanism for biodiesel components methyl stearate and methyl oleate

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    Detailed chemical kinetic reaction mechanism for biodiesel components methyl stearate and methyl are developed for two of the five major components of biodiesel fuel, methyl stearate and methyl oleate renewable sources, can reduce net emissions of greenhouse gases. An important class of biodiesel fuels

  19. MTBE/methanol supply

    SciTech Connect (OSTI)

    Simmons, R.E.

    1986-05-01T23:59:59.000Z

    U.S. methanol production has become economically competitive with imports due to de-escalation of natural gas price from $3.07 mm Btu in January 1985 to $2.07 mm Btu by December 1985. This has reversed the earlier supply outlook when it appeared that additional methanol plants would shutdown due to low cost imports. Current gas cost in conjunction with projections for continued excess supply prompted DuPont to restart their 250 mm gpy plant at Beaumont, Texas. Other former producers are contemplating restarting idle units.

  20. alkyl-tert alkyl ethers: Topics by E-print Network

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

    TREAT METHYL- TERT-BUTYL ETHER CONTAMINATED CiteSeer Summary: Methyl-tert-butyl ether (MTBE) is a commonly used gasoline additive. Leaking underground storage tank systems,...

  1. Detailed Chemical Kinetic Reaction Mechanism for Biodiesel Components Methyl Stearate and Methyl Oleate

    SciTech Connect (OSTI)

    Naik, C; Westbrook, C K; Herbinet, O; Pitz, W J; Mehl, M

    2010-01-22T23:59:59.000Z

    New chemical kinetic reaction mechanisms are developed for two of the five major components of biodiesel fuel, methyl stearate and methyl oleate. The mechanisms are produced using existing reaction classes and rules for reaction rates, with additional reaction classes to describe other reactions unique to methyl ester species. Mechanism capabilities were examined by computing fuel/air autoignition delay times and comparing the results with more conventional hydrocarbon fuels for which experimental results are available. Additional comparisons were carried out with measured results taken from jet-stirred reactor experiments for rapeseed methyl ester fuels. In both sets of computational tests, methyl oleate was found to be slightly less reactive than methyl stearate, and an explanation of this observation is made showing that the double bond in methyl oleate inhibits certain low temperature chain branching reaction pathways important in methyl stearate. The resulting detailed chemical kinetic reaction mechanism includes more approximately 3500 chemical species and more than 17,000 chemical reactions.

  2. Waiver of Preferential Right to Lease Highway Right of Way | Open Energy

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are beingZealand Jump to:Ezfeedflag JumpID-fTri Global EnergyUtilityInformation Waiver of Preferential Right to

  3. DOE Issues Enforcement Guidance on Large-Capacity Clothes Washer Waivers

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

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels DataDepartment of Energy Your Density Isn't Your Destiny: Theof"Wave theJulyD&DDepartment of EnergyFederaland the Waiver

  4. International Journal of Mass Spectrometry 249250 (2006) 303310 Pyrolysis of 2-methoxy-2,3,3-trimethylbutane (MTMB) monitored by

    E-Print Network [OSTI]

    Morton, Thomas Hellman

    used fuel oxygenates MTBE and TAME), the predominance of bond homolysis at temperatures >900 K suggests homologues ­ methyl tert-butyl ether (MTBE) and tert-amyl methyl ether (TAME) ­ present a new set of problems discussed as alternatives to MTBE and TAME, because they are expected to be much less soluble in water. More

  5. UNIVERSITY OF CALIFORNIA Santa Barbara

    E-Print Network [OSTI]

    California at Santa Barbara, University of

    , B. Dooher, and D. Rice, Analysis of dissolved benzene plumes and methyl tertiary butyl ether (MTBE, An evaluation of MTBE impacts to California groundwater resources, pp. 68 p., Lawrence Livermore National, Temporal Analysis of Methyl Tertiary Butyl Ether (MTBE) Plumes at California Leaking Underground Fuel tank

  6. EINLADUNG INFOTAG 2001 Eine Forschungsanstalt

    E-Print Network [OSTI]

    Wehrli, Bernhard

    durch den Benzinzusatz MTBE. Methyl-tert-butylether gehört weltweit zu den meistproduzierten orga- nischen Chemikalien. Weil MTBE im Grundwasser auftritt, soll es in den USA als Benzinzusatz verboten

  7. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Aug. 2004, p. 47204726 Vol. 70, No. 8 0099-2240/04/$08.00 0 DOI: 10.1128/AEM.70.8.47204726.2004

    E-Print Network [OSTI]

    Alvarez, Pedro J.

    contamination of surface and groundwater resources by the gasoline oxygenate methyl tert-butyl ether (MTBE) is leading to its phaseout. Ethanol, a likely candidate to substitute MTBE, is increasingly being used

  8. Gas Chromatography -Mass Spectrometry

    E-Print Network [OSTI]

    Nizkorodov, Sergey

    , ethanol and methyl-t-butyl ether (MTBE). Due to some gasoline leakage from underground storage tanks into drinking water supplies, MTBE has been, or is in the process of being phased out in many areas. The octane

  9. Texas Rice, Volume V, Number 5

    E-Print Network [OSTI]

    environmental lawsuits because one of their products, the gasoline additive MTBE, has con- taminated drinking water in hundreds of communities. House leaders have insisted an MTBE waiver be part of energy legislation. There have been discussions among House... Repub- licans to establish a federal fund for MTBE cleanup along with liability protection for the manufactures. President Bush praised the Senate for passing the measure, saying it would help U.S. economic growth by addressing the causes of high energy...

  10. Isothermal vapor-liquid equilibria for 2-methyl-2-butanol + 2-methyl-1-butanol + 1-pentanol

    SciTech Connect (OSTI)

    Aucejo, A.; Burguet, M.C.; Monton, J.B.; Munoz, R.; Sanchotello, M.; Vazquez, M.I. (Univ. of Valencia (Spain). Dept. de Ingenieria Quimica)

    1994-07-01T23:59:59.000Z

    Vapor-liquid equilibria (VLE) for 2-methyl-2-butanol + 2-methyl-1-butanol and 2-methyl-2-butanol + 2-methyl-1-butanol + 1-pentanol have been measured at 373.15 K. The binary VLE results have been correlated by different liquid-phase activity coefficient models. The binary interaction parameters obtained from Wilson, NRTL, and UNIQUAC models in this and a previously study are used to predict the VLE data for the ternary system. Vapor-liquid equilibrium (VLE) data are necessary for the design of distillation processes.

  11. Growing season methyl bromide and methyl chloride fluxes at a sub-arctic wetland in Sweden

    E-Print Network [OSTI]

    Hardacre, Catherine J.; Blei, Emanuel; Heal, Mathew R

    2009-01-01T23:59:59.000Z

    Methyl bromide and methyl chloride fluxes were measured at several sites in a sub-arctic wetland near Abisko, Sweden (6828?N 1849?E) throughout the 2008 growing season. Averaged over 92 flux measurements the sub-arctic wetland was found to be a...

  12. 3-Methyl-1-butanol production in Escherichia coli: random mutagenesis and two-phase fermentation

    E-Print Network [OSTI]

    Connor, Michael R.; Cann, Anthony F.; Liao, James C.

    2010-01-01T23:59:59.000Z

    biosynthesis and 3-methyl-1-butanol production. All genesCELL PHYSIOLOGY 3-Methyl-1-butanol production in Escherichiathe production of 3-methyl-1-butanol by leveraging selective

  13. Comparative Dynamics of Leucine Methyl Groups in FMOC-Leucine...

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

    Dynamics of Leucine Methyl Groups in FMOC-Leucine and in a ProteinHydrophobic Core Probed by Solid-State Deuteron Comparative Dynamics of Leucine Methyl Groups in FMOC-Leucine and...

  14. Sub-millimeter sized methyl butanoate droplet combustion: Microgravity experiments

    E-Print Network [OSTI]

    Walter, M.Todd

    -dependent, sphero-symmetric droplet combustion simulation that includes detailed gas phase chemical kineticsSub-millimeter sized methyl butanoate droplet combustion: Microgravity experiments and detailed 2012 Abstract Combustion characteristics of isolated sub-millimeter sized methyl butanoate (MB

  15. Vapor-liquid equilibria for systems of 1-butanol with 2-methyl-1-butanol, 3-methyl-1-butanol, 2-methyl-2-butanol, and 3-methyl-2-butanol at 30 and 100 kPa

    SciTech Connect (OSTI)

    Aucejo, A.; Burguet, M.C.; Monton, J.B.; Munoz, R.; Sanchotello, M.; Vazquez, M.I. (Univ. de Valencia (Spain). Dept. de Ingenieria Quimica)

    1994-04-01T23:59:59.000Z

    Vapor-liquid equilibrium data were measured for binary systems of 1-butanol with 2-methyl-1-butanol, 3-methyl-1-butanol, 2-methyl-2-butanol, and 3-methyl-2-butanol at 30 and 100 kPa. The experimental data obtained in this work are thermodynamically consistent according to a point-to-point consistency test, and deviation from ideal behavior is small in all cases. They can be equally well correlated with the Margules, Van Laar, Wilson, NRTL, and UNIQUAC equations.

  16. Bioreactors for Removing Methyl Bromide following Contained

    E-Print Network [OSTI]

    Bioreactors for Removing Methyl Bromide following Contained Fumigations L A U R E N C E G . M I L L contributes to the depletion of stratospheric ozone. A closed-system bioreactor consisting of 0.5 L recirculating air. Strain IMB-1 grew slowly to high cell densities in the bioreactor using MeBr as its sole

  17. DNA methylation and the analysis of CpG Islands

    E-Print Network [OSTI]

    Czygrinow, Andrzej

    DNA methylation and the analysis of CpG Islands in genomes M. F. Wojciechowski MAT 351 25 March 2005 #12;#12;Nucleotides #12;Base pairing * * #12;DNA methylation In mammalian genomes, methylation residues represent a target for covalent modification of DNA Cytosine is one of two bases found commonly

  18. PROOF COPY [023113] 008209QEE [023113]008209QEE

    E-Print Network [OSTI]

    Alvarez, Pedro J.

    as a replacement for the gasoline oxygenate, methyl tert-butyl ether MTBE , may lead to indirect impacts related facilitate the migration of pre-existing contamination. MTBE 25 mg/L influent was not degraded inlet by one order of magnitude relative to columns fed BTEX alone or with MTBE. However, 16S

  19. Environmental Toxicology and Chemistry, Vol. 21, No. 12, pp. 26312639, 2002 Printed in the USA

    E-Print Network [OSTI]

    Alvarez, Pedro J.

    --Aquifer microcosms were used to determine how ethanol and methyl-tert-butyl ether (MtBE) affect monoaromatic compared to benzene, which was degraded only under aerobic conditions. The MtBE was not degraded within 100 to phase out MtBE as a gasoline oxy- genate is likely to significantly increase the use of ethanol

  20. Critical Reviews in Environmental Science and Technology, 00(0):000000 (2001) 1064-3389/01/$.50

    E-Print Network [OSTI]

    Alvarez, Pedro J.

    water contamination by methyl tert-butyl ether (MTBE) have made policymakers more cognizant of the need reformulated gasoline (RFG) (2% oxygen) year-round to reduce emissions that contribute to ozone formation. MTBE-making process that lead to the widespread use of MTBE over the last decade is now quite controversial (BRP, 1999

  1. Monitoring synaptic protein dynamics with higher temporal, spatial, and molecular resolution

    E-Print Network [OSTI]

    Butko, Margaret

    2012-01-01T23:59:59.000Z

    Spectrometry mSOG MiniSOG MTBE Methyl tert-butyl ether mTORMethyl tert-butyl ether (MTBE, 1.4 mL) was then added for1,000 g, 5 min). The MTBE layer was collected into a 1.5-mL

  2. I. Pt-Catalyzed Tandem Epoxide Fragmentation/Pentannulation of Propargylic Esters II. Progress Toward the Kopsia Family of Indole Alkaloids

    E-Print Network [OSTI]

    Pujanauski, Brian Gerard

    2010-01-01T23:59:59.000Z

    methyl t-butyl ether (MTBE), a much more environmentallyPhMe, reflux POCl 3 , Et 3 N CN MTBE Scheme 3.3: OptimizedO H NH POCl 3 , Et 3 N CN MTBE 1-Isocyanocyclohex-1-ene (

  3. Effects of oxygenate concentration on species mole fractions in premixed n-heptane flames

    E-Print Network [OSTI]

    Senkan, Selim M.

    -heptane/oxygenate mixtures were 2.7 and 3.4. Three different fuel oxygenates (i.e. MTBE, methanol, and ethanol) were tested tertiary-butyl ether (MTBE), ethyl tertiary-butyl ether (ETBE), and tertiary amyl methyl ether (TAME)) were considered as possible fuel oxygenates. MTBE and ethanol are the most common oxygenates currently used

  4. ETHANOL FROM CORN: CLEAN RENEWABLE FUEL FOR THE FUTURE, OR DRAIN ON OUR RESOURCES AND POCKETS?

    E-Print Network [OSTI]

    Patzek, Tadeusz W.

    , and by law refiners must add to gasoline oxygenating additives like methyl ter- tiary-butyl ether (MTBE better, thus reducing carbon monoxide and other emissions. MTBE is the fuel oxygenate preferred by oil as gaso- line, mixes well with gasoline, and does not increase the gasoline vapor pressure. MTBE has

  5. Fourier Transform Infrared Spectroscopy

    E-Print Network [OSTI]

    Nizkorodov, Sergey

    FTIR - 1 Fourier Transform Infrared Spectroscopy FTIR DETERMINATION OF MTBE IN GASOLINE AND ETHANOL FTIR DETERMINATION OF MTBE IN GASOLINE AND ETHANOL IN VODKA AND MOUTHWASH INTRODUCTION As a part has contained MTBE (methyl tert­butyl ether) as its primary oxygenate. However, there has been

  6. DNA Methylation as a Biomarker for Preeclampsia

    SciTech Connect (OSTI)

    Anderson, Cindy M.; Ralph, Jody L.; Wright, Michelle L.; Linggi, Bryan E.; Ohm, Joyce E.

    2014-10-01T23:59:59.000Z

    Background: Preeclampsia contributes significantly to pregnancy-associated morbidity and mortality as well as future risk of cardiovascular disease in mother and offspring, and preeclampsia in offspring. The lack of reliable methods for early detection limits the opportunities for prevention, diagnosis, and timely treatment. Purpose: The purpose of this study was to explore distinct DNA methylation patterns associated with preeclampsia in both maternal cells and fetal-derived tissue that represent potential biomarkers to predict future preeclampsia and inheritance in children. Method: A convenience sample of nulliparous women (N = 55) in the first trimester of pregnancy was recruited for this prospective study. Genome-wide DNA methylation was quantified in first-trimester maternal peripheral white blood cells and placental chorionic tissue from normotensive women and those with preeclampsia (n = 6/group). Results: Late-onset preeclampsia developed in 12.7% of women. Significant differences in DNA methylation were identified in 207 individual linked cytosine and guanine (CpG) sites in maternal white blood cells collected in the first trimester (132 sites with gain and 75 sites with loss of methylation), which were common to approximately 75% of the differentially methylated CpG sites identified in chorionic tissue of fetal origin. Conclusion: This study is the first to identify maternal epigenetic targets and common targets in fetal-derived tissue that represent putative biomarkers for early detection and heritable risk of preeclampsia. Findings may pave the way for diagnosis of preeclampsia prior to its clinical presentation and acute damaging effects, and the potential for prevention of the detrimental long-term sequelae.

  7. MTBE, Oxygenates, and Motor Gasoline

    Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645 3,625 1,006 492 742 33 111 1,613 122 40 Buildingto17 3400, U.S.MajorMarketsNov-14Biomass feedstocks

  8. Oxidation and methylation of dissolved elemental mercury by anaerobic bacteria

    SciTech Connect (OSTI)

    Hu, Haiyan [ORNL] [ORNL; Lin, Hui [ORNL] [ORNL; Zheng, Wang [ORNL] [ORNL; Tomanicek, Stephen J [ORNL] [ORNL; Johs, Alexander [ORNL] [ORNL; Feng, Xinbin [ORNL] [ORNL; Elias, Dwayne A [ORNL] [ORNL; Liang, Liyuan [ORNL] [ORNL; Liang, Liyuan [ORNL] [ORNL; Gu, Baohua [ORNL] [ORNL

    2013-01-01T23:59:59.000Z

    Methylmercury is a neurotoxin that poses significant health risks to humans. Some anaerobic sulphate- and iron-reducing bacteria can methylate oxidized forms of mercury, generating methylmercury1-4. One strain of sulphate-reducing bacteria (Desulfovibrio desulfuricans ND132) can also methylate elemental mercury5. The prevalence of this trait among different bacterial strains and species remains unclear, however. Here, we compare the ability of two strains of the sulphate-reducing bacterium Desulfovibrio and one strain of the iron-reducing bacterium Geobacter to oxidise and methylate elemental mercury in a series of laboratory incubations. Experiments were carried out under dark, anaerobic conditions, in the presence of environmentally-relevant concentrations of elemental mercury. We report differences in the ability of these organisms to oxidise and methylate elemental mercury. In line with recent findings5, we show that Desulfovibrio desulfuricans ND132 can both oxidise and methylate elemental mercury. However, the rate of methylation of elemental mercury is only about one third the rate of methylation of oxidized mercury. We also show that Desulfovibrio alaskensis G20 can oxidise, but not methylate, elemental mercury. Geobacter sulfurreducens PCA is able to oxidise and methylate elemental mercury in the presence of cysteine. We suggest that the activity of methylating and non-methylating bacteria may together enhance the formation of methylmercury in anaerobic environments.

  9. Conference Waiver

    Office of Environmental Management (EM)

    current events and issues of concern to DOE Emergency Management. Events such as Fukushima, the wild-land fires, and other catastrophic disasters have uncovered issues that...

  10. Conference Waiver

    Office of Environmental Management (EM)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645 3,625 1,006 492 742 33 1112011AT&T, Inc.'sEnergyTexas1.Space DataEnergyCompressedOil, and Gas| Department

  11. aromatic compound mixtures: Topics by E-print Network

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

    and mineralization potentials of gasoline monoaromatics and methyl tert-butyl ether (MTBE), compounds that commonly co-exist in groundwater contaminant plumes. A mixed culture...

  12. Water Quality

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

    which can lead to public health problems. * MtBE (Methyl tert Butyl Ether), a gasoline additive, has begun to contaminate ground water supplies. * Similarly, perchlorate has...

  13. This journal is c the Owner Societies 2012 Phys. Chem. Chem. Phys., 2012, 14, 675680 675 Cite this: Phys. Chem. Chem. Phys., 2012, 14, 675680

    E-Print Network [OSTI]

    Neumark, Daniel M.

    -octane and in the oxidation of fuel additives such as MTBE and ETBE (methyl and ethyl t-butyl ether).1 The chemistry

  14. The University of Stirling Vietnam Award This award offers a fee waiver of 1,000 for the first year and 500 for years two,

    E-Print Network [OSTI]

    Little, Tony

    The University of Stirling Vietnam Award This award offers a fee waiver of 1,000 for the first-time undergraduate or postgraduate (taught or research) degree. The University of Stirling wishes to offer this award at Stirling and add to our already diverse international community on campus. Students do not have to apply

  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

    2010-02-19T23:59:59.000Z

    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. aromatic hydrocarbons methyl: Topics by E-print Network

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

    with electrophiles allows preparation of (more) Savla, Paresh M. 1993-01-01 2 Infrared spectra of methyl-, and nitrogen-modified void coronene; modeling a carrier of...

  17. Methyl viologen radical reactions with several oxidizing agents. [Gamma Radiation

    SciTech Connect (OSTI)

    Levey, G.; Ebbesen, T.W.

    1983-01-01T23:59:59.000Z

    The rates of oxidation of the methyl viologen radical by peroxodisulfate and hydrogen peroxide has been investigated. The methyl viologen free radical was produced by pulse radiolysis. The reaction of the peroxodisulfate radical with the methyl viologen radical was first order in both species, and the reaction rate constant is reported. A el-radiation study revealed a chain decomposition of the peroxodisulfate radical involving the methyl viologen radical when methanol, ethanol, or 2-propanol was present. Loss of the methyl viologen radical was then no longer observed to be a simple first-order reaction. The reaction of hydrogen peroxide with the methyl viologen radical was very slow in the presence of 1 M methanol. A much faster reaction in the absence of methanol was interpreted to be a reaction of the methyl viologen radical with the peroxy radicals. Hydrogen peroxide, in contrast to the chain decomposition of peroxodisulfate radicals, does not participate in a chain reaction involving the methyl viologen radical and methanol. Rate constants for the reaction of methyl viologen radical with dichromate radical, iodate radical, and ferricyanide radical are reported.

  18. Major sources to waivers - lessons learned and $ saved at two U.S. Navy facilities

    SciTech Connect (OSTI)

    Klitsch, M. [Naval Surface Warfare Center, West Bethesda, MD (United States). Carderock Div.

    1997-12-31T23:59:59.000Z

    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.

  19. Genome Sequence of Mercury-Methylating and Pleomorphic Desulfovibrio africanus

    E-Print Network [OSTI]

    Genome Sequence of Mercury-Methylating and Pleomorphic Desulfovibrio africanus Contact: Steven D. africanus genome sequence to allow us to gain insights into the physiological states genomics using the sequence information for D. africanus and the previously sequenced mercury methylator D

  20. 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. (Berkeley, CA); Keasling, Jay D. (Berkeley, CA)

    2011-07-26T23:59:59.000Z

    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.

  1. DNA methylation dynamics of the human preimplantation embryo

    E-Print Network [OSTI]

    Smith, Zachary D.

    In mammals, cytosine methylation is predominantly restricted to CpG dinucleotides and stably distributed across the genome, with local, cell-type-specific regulation directed by DNA binding factors. This comparatively ...

  2. akap12 promoter methylation: Topics by E-print Network

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

    (MEK) with hydrogen peroxide (H2O2), is widely used in industry as a radicalThermal Hazard Analysis of Methyl Ethyl Ketone Peroxide Ron-Hsin Chang, Chi-Min Shu and Po-Yin Yeh...

  3. ENVIRONMENTAL BIOTECHNOLOGY Biodegradation of methyl parathion and p-nitrophenol

    E-Print Network [OSTI]

    Merrick, Mike

    ENVIRONMENTAL BIOTECHNOLOGY Biodegradation of methyl parathion and p-nitrophenol: evidence material Supplementary material is available in the online version of this article at http://dx.doi.org/ 10

  4. Methyl arsenic adsorption and desorption behavior on iron oxides

    E-Print Network [OSTI]

    Lafferty, Brandon James

    2005-08-29T23:59:59.000Z

    of the widespread distribution and toxicity of arsenic and methyl-arsenic, their adsorption behavior on soil minerals is of great interest. Although considerable attention has been given to the behavior of inorganic arsenic on mineral surfaces, little research has...

  5. Regulation of yeast development by mRNA methylation

    E-Print Network [OSTI]

    Agarwala, Sudeep D

    2012-01-01T23:59:59.000Z

    The internal methylation of mRNA post-transcriptionally is an essential component of the mRNA editing machinery in virtually every eukaryotic system. Despite this ubiquity, little is known about the relevance, consequences ...

  6. Methyl bromide emissions to the atmosphere from temperate woodland ecosystems

    E-Print Network [OSTI]

    Drewer, Julia; Heal, Kate V; Smith, Keith A; Heal, Mathew R

    2008-01-01T23:59:59.000Z

    The environmental importance of methyl bromide (CH3Br) arises from its contribution to stratospheric ozone loss processes and, as a consequence, its emissions from anthropogenic sources are subject to the Montreal Protocol. A better understanding...

  7. The synthesis of some N-methylated aminoalkylphosphonic acids

    E-Print Network [OSTI]

    Eikenberry, Jon Nathan

    1966-01-01T23:59:59.000Z

    THE SYNTHESIS OF SOME N-METHYLATED AMINOALKYLPHOSFHONIC ACIDS A Thesis By JON NATHAN EIKENBERRY Submitted to the Graduate College of the Texas ARM University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE... August 1966 Major Subject: Chemistry THE SYNTHESIS OF SOME N-METHYLATED AMINOALKYLPHOSPHONlc ACIDS A Thesis By ION NATHAN EIKENBERRY Approved as to styl and content by: (Chairman of Committee) (Hea f Department) (Member) (Member) August 1966...

  8. 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.

    2005-09-29T23:59:59.000Z

    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.

  9. Phytoremediation of ionic and methyl mercury pollution

    SciTech Connect (OSTI)

    Meagher, R.B.

    1998-06-01T23:59:59.000Z

    '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.'

  10. Nested methylation-specific polymerase chain reaction cancer detection method

    DOE Patents [OSTI]

    Belinsky, Steven A. (Albuquerque, NM); Palmisano, William A. (Edgewood, NM)

    2007-05-08T23:59:59.000Z

    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.

  11. Methods for detection of methyl-CpG dinucleotides

    DOE Patents [OSTI]

    Dunn, John J.

    2013-01-29T23:59:59.000Z

    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.

  12. Methods for detection of methyl-CpG dinucleotides

    DOE Patents [OSTI]

    Dunn, John J.

    2012-09-11T23:59:59.000Z

    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.

  13. Methods for detection of methyl-CpG dinucleotides

    DOE Patents [OSTI]

    Dunn, John J

    2013-11-26T23:59:59.000Z

    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.

  14. Freezing of Dynamics of a Methyl Group in a Protein Hydrophobic...

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

    Freezing of Dynamics of a Methyl Group in a Protein Hydrophobic Core at Cryogenic Temperatures by Deuteron NMR Spectroscopy. Freezing of Dynamics of a Methyl Group in a Protein...

  15. Environmental and age effects on methylation changes in human brain and blood cells

    E-Print Network [OSTI]

    Giguzinsky, Orit

    2014-01-01T23:59:59.000Z

    Previous studies have shown that DNA methylation may 1 e associated with disease, aging, the rate of aging and genetics. In this thesis, age is accurately predicted from DNA methylation in brain and blood tissues using two ...

  16. Photodegradation in a stress and response framework: poly(methyl

    E-Print Network [OSTI]

    Rollins, Andrew M.

    (methyl methacrylate); photovoltaics; degradation. Paper 12020SS received Mar. 21, 2012; revised manuscript received of photovoltaics (PV) lifetime and degradation science (L&DS)24 as a critical scientific challenge for robust of materials for enhanced photovoltaic (PV) performance, it is critical to have quantitative knowledge of both

  17. The synthesis of some N-methylated aminoalkylphosphonic acids

    E-Print Network [OSTI]

    Eikenberry, Jon Nathan

    1966-01-01T23:59:59.000Z

    -Di- methylamino-1-alkenes Diethyl I-Dimethylamino-2-methylpropyl- phosphonate Diethyl 1-Dimethylaminobutylphosphonate . Diethyl 1-Dimethylamino-3-methylbutyl- phosphonate General Procedure for the Preparation of 1-Dimethyl...'-Tetramethyldi- aminomethane 66 Infrared Spectrum of Benzylidene-bis-dimethyl- amine 66 Infrared Spectrum of 1-Dimethylamino-2-methyl- 1-propene . . . . . . . . . . . . . . . . . . . 67 Infrared Spectrum of 1-Dimethylamino-1-butene . . 67 Infrared Spectrum of I...

  18. Phase 1 Methyl Iodide Deep-Bed Adsorption Tests

    SciTech Connect (OSTI)

    Nick Soelberg; Tony Watson

    2014-08-01T23:59:59.000Z

    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.

  19. An evaluation of the 3M Organic Vapor Monitor #3500 as a short term exposure limit sampling device for acetone, methyl ethyl ketone, and methyl iso butyl ketone

    E-Print Network [OSTI]

    Andrew, Lloyd B.

    1982-01-01T23:59:59.000Z

    AN EVALUATION OF THE 3M ORGANIC VAPOR MONITOR 43500 AS A SHOR'I TERM EXPOSURE LIMIT SAMPLING DEVICE FOR ACETONE, METHYL ETHYL KETONE, AND METHYL ISO BUTYL KETONE A Thesis by LLOYD B. ANDREW III Submitted to the Graduate College of Texas ASM..., METHYL ETHYL KETONE, AND METHYL ISO BUTYL KETONE A Thesis by Lloyd B. Andrew III Approved as to style and content by: (Chai iy' of Co ' i tee) (He of Departme t) e4mY ~. (Member) C~& n (Member) December 1982 ABSTRACT An Evaluation of the 3M...

  20. Eliminating MTBE in Gasoline in 2006

    Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645 3,625 1,006 492 742 33 111 1,613 122 40Coal Stocks at1,066,688Electricity Use as an Indicator of U.S. Economic Activity1

  1. Motor Gasoline Outlook and State MTBE Bans

    Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645 3,625 1,006 492 742 33 111 1,613 122 40 Buildingto17 3400,Information Administration22)May 28, 1996September

  2. Mercury Methylation in Mine Wastes Collected from Abandoned Mercury Mines in the USA

    SciTech Connect (OSTI)

    Gray, John E. (U.S. Geological Survey); Hines, Mark E. (Massachusetts, Univ Of); Biester, Harald (Heidelberg College); Lasorsa, Brenda K. (BATTELLE (PACIFIC NW LAB))

    2003-05-01T23:59:59.000Z

    Mercury mines contain highly elevated Hg contents, but more problematic environmentally are elemental Hg and soluble Hg salts produced during ore retorting that remain in wastes at mine sites. Under certain conditions, these inorganic Hg compounds convert to bioavailable, highly toxic organic Hg forms. Speciation and transformation of Hg was studied in wastes collected from abandoned Hg mines at McDermitt, NV, and Terlingua, TX, which are moderate size on an international scale and produced about 10,000 and 5,000 t of elemental Hg, respectively. In waste samples, we measured total Hg and methyl-Hg contents, identified various Hg compounds using Hg-thermo-desorption pyrolysis, and determined rates of Hg methylation and methyl-Hg demethylation using isotopic-tracer methods. Pyrolysis analysis of mine wastes showed variable amounts of cinnabar, metacinnabar, Hg salts, elemental Hg, and elemental Hg sorbed onto particulates such as clay and Fe-oxides. Mine wastes with the highest methyl-Hg contents correspond to those with elemental Hg and particulate-sorbed elemental Hg, and also produced the highest laboratory-estimated potential Hg methylation rates, as much as 4.8%/day. Samples containing dominantly cinnabar showed little or no Hg methylation. Mine wastes with high methyl-Hg contents generally showed low methyl-Hg demethylation, suggesting that Hg methylation was dominant. Both mines are located in semiarid climates, and during this study, streambeds below the mines were dry. Total Hg contents in stream sediment collected below the mines show significant dilution, and methyl-Hg contents were typically below the limit of determination. Methylation of Hg downstream from Hg mines is probably lower in arid climates due to lack of mine-water runoff and lower microbial activity. The correspondence of mine wastes containing elemental Hg and high methyl-Hg contents suggests that Hg0 oxidizes to Hg2+, which is subsequently bioavailable for microbial Hg methylation.

  3. Proton NMR analysis of octane number for motor gasoline: Part V

    SciTech Connect (OSTI)

    Ichikawa, M.; Nonaka, N.; Amano, H.; Takada, I.; Ishimori, S. [Suzuki Motor Corp., Hamamatsu (Japan); Andoh, H.; Kumamoto, K. [Showa Shell Sikiyu Tokyo (Japan)

    1992-10-01T23:59:59.000Z

    A method to predict the octane number of automobile gasoline containing methyl tert-butyl ether (MTBE) by proton magnetic resonance (PMR) spectrometry was studied. Samples of gasoline whose octane numbers had been identified according to the ASTM standards (commercially available premium gasoline to which MTBE was added at rates of 7 vol % and 14 vol %) were used in this investigation of the effect of MTBE on the octane number. The findings were utilized to introduce a term regarding MTBE into the previously reported linear regression equation for estimating the octane number from the PMR spectrum, and the appropriateness of the linear regression equation was assessed. As a result the MTBE contents in the sample were determined with satisfactory accuracy by using a standard addition method, and a linear regression equation reflecting the effect of MTBE was obtained. These achievements are reported. 11 refs., 3 figs., 5 tabs.

  4. Technical Review Report for the Mound 1KW Package Safety Analysis Report for Packaging Waiver for the Use of Modified Primary Containment Vessel (PCV)

    SciTech Connect (OSTI)

    West, M; Hafner, R

    2008-05-05T23:59:59.000Z

    This Technical Review Report (TRR) documents the review, performed by the Lawrence Livermore National Laboratory (LLNL) staff, at the request of the U.S. Department of Energy (DOE), on the Waiver for the Use of Modified Primary Containment Vessels (PCV). The waiver is to be used to support a limited number of shipments of fuel for the Multi-Mission Radioisotope Thermoelectric Generator (MMRTG) Project in support of the National Aeronautics and Space Administration's (NASA's) Mars Science Laboratory (MSL) mission. Under the waiver, an inventory of existing national security PCVs will be converted to standard PCVs. Both types of PCVs are currently approved for use by the Office of Nuclear Energy. LLNL has previously reviewed the national security PCVs under Mound 1KW Package Safety Analysis Report for Packaging, Addendum No. 1, Revision c, dated June 2007 (Addendum 1). The safety analysis of the package is documented in the Safety Analysis Report for Packaging (SARP) for the Mound 1KW Package (i.e., the Mound 1KW SARP, or the SARP) where the standard PCVs have been reviewed by LLNL. The Mound 1KW Package is certified by DOE Certificate of Compliance (CoC) number USA/9516/B(U)F-85 for the transportation of Type B quantities of plutonium heat source material. The waiver requests an exemption, claiming safety equivalent to the requirements specified in 10 CFR 71.12, Specific Exemptions, and will lead to a letter amendment to the CoC. Under the waiver, the Office of Radioisotope Power Systems, NE-34, is seeking an exemption from 10 CFR 71.19(d)(1), Previously Approved Package,[5] which states: '(d) NRC will approve modifications to the design and authorized contents of a Type B package, or a fissile material package, previously approved by NRC, provided--(1) The modifications of a Type B package are not significant with respect to the design, operating characteristics, or safe performance of the containment system, when the package is subjected to the tests specified in {section}71.71 and 71.73.' The LLNL staff had previously reviewed a request from Idaho National Laboratory (INL) to reconfigure national security PCVs to standard PCVs. With a nominal 50% reduction in both the height and the volume, the LLNL staff initially deemed the modifications to be significant, which would not be allowed under the provisions of 10 CFR 71.19(d)(1)--see above. As a follow-up, the DOE requested additional clarification from the Nuclear Regulatory Commission (NRC). The NRC concluded that the reconfiguration would be a new fabrication, and that an exemption to the regulations would be required to allow its use, as per the requirements specified in 10 CFR 71.19(c)(1), Previously Approved Package: '(c) A Type B(U) package, a Type B(M) package, or a fissile material package previously approved by the NRC with the designation '-85' in the identification number of the NRC CoC, may be used under the general license of {section}71.17 with the following additional conditions: (1) Fabrication of the package must be satisfactorily completed by December 31, 2006, as demonstrated by application of its model number in accordance with 71.85(c).' Although the preferred approach toward the resolution of this issue would be for the applicant to submit an updated SARP, the applicant has stated that the process of updating the Model Mound 1KW Package SARP is a work that is in progress, but that the updated SARP is not yet ready for submittal. The applicant has to provide a submittal, proving that the package meets the '-96' requirements of International Atomic Energy Agency (IAEA) Safety Standards Series No. TS-R-1, in order to fabricate approved packagings after December 31, 2006. The applicant has further stated that all other packaging features, as described in the currently approved Model Mound 1KW Package SARP, remain unchanged. This report documents the LLNL review of the waiver request. The specific review for each SARP Chapter is documented.

  5. Durability of Poly (Methyl Methacrylate) Lenses Used in Concentrating Photovoltaics (Presentation)

    SciTech Connect (OSTI)

    Miller, D.; Gedvilas, L.; To, B.; Kennedy, C.; Kurtz, S.

    2010-10-21T23:59:59.000Z

    This presentation reports the findings of NREL's screen test to characterize the durability of poly (methyl methacrylate) lenses used in concentrated photovoltaics.

  6. antioxidant butylated hydroxytoluene: Topics by E-print Network

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

    by Fusarium solani CiteSeer Summary: Fusarium solani degraded methyl tert-butyl ether (MTBE) and other oxygenated compounds from gasoline including tert-butyl alcohol (TBA). The...

  7. alkyl tert-butyl ether: Topics by E-print Network

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

    by Fusarium solani CiteSeer Summary: Fusarium solani degraded methyl tert-butyl ether (MTBE) and other oxygenated compounds from gasoline including tert-butyl alcohol (TBA). The...

  8. ammoniated glycyrrhizin butylated: Topics by E-print Network

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

    by Fusarium solani CiteSeer Summary: Fusarium solani degraded methyl tert-butyl ether (MTBE) and other oxygenated compounds from gasoline including tert-butyl alcohol (TBA). The...

  9. APPENDXD.CHP:Corel VENTURA

    Annual Energy Outlook 2013 [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...

  10. Surface pre-coating of talc particles by carboxyl methyl cellulose adsorption : study of adsorption

    E-Print Network [OSTI]

    Paris-Sud XI, Universit de

    1 Surface pre-coating of talc particles by carboxyl methyl cellulose adsorption : study of adsorption and consequences on surface properties and settling rate P. Bacchin1 , J-P. Bonino2 , F. Martin3 This paper investigates the adsorption of different sized carboxyl methyl cellulose (CMC) onto talc particles

  11. Arsenic Methylation and Bladder Cancer Risk in CaseControl Studies in Argentina and the

    E-Print Network [OSTI]

    California at Berkeley, University of

    Arsenic Methylation and Bladder Cancer Risk in Case­Control Studies in Argentina and the United's susceptibility to bladder cancer. Methods: Urinary methylation products were measured in subjects from Argentina (114 cases and 114 controls) and the United States (23 cases and 49 controls). Results: In Argentina

  12. Molecular Dynamics of Methylamine, Methanol, and Methyl Fluoride Cations in Intense 7 Micron Laser Fields

    E-Print Network [OSTI]

    Schlegel, H. Bernhard

    Molecular Dynamics of Methylamine, Methanol, and Methyl Fluoride Cations in Intense 7 Micron Laser of methylamine (CH3NH2 + ), methanol (CH3OH+ ), and methyl fluoride (CH3F+ ) cations by short, intense laser 7 m laser pulses. This work is motivated by recent studies of methanol cations by Yamanouchi and co

  13. A neutron diffraction study of bis(cyclopentadienyl)(methyl)(methylene)tantalum(V) at 15 K

    E-Print Network [OSTI]

    Takusagawa, Fusao

    1988-01-01T23:59:59.000Z

    (4) A] in the methyl group is slightly longer than that in the methylene group [1-081 (5) A], while therespective H-C-H angles are 107-8(3) (methyl, mean value) and 112-3(2) (methylene). The Ta-C methylene distance is 2-039 (1) A, corresponding to a...

  14. Mechanisms Regulating Mercury Bioavailability for Methylating Microorganisms in the Aquatic Environment: A Critical Review

    E-Print Network [OSTI]

    in aquatic food webs is the methylation of inorganic forms of the metal, a process that is primarily mediated methylation occurs and the processes that control mercury bioavailability to these organisms. Methylmercury, and natural organic matter. These interactions result in a mixture of dissolved, nanoparticulate, and larger

  15. Regulation of N-Methyl-D-aspartic Acid (NMDA) Receptors by Metabotropic Glutamate Receptor 7*

    E-Print Network [OSTI]

    Yan, Zhen

    Regulation of N-Methyl-D-aspartic Acid (NMDA) Receptors by Metabotropic Glutamate Receptor 7-methyl-D-aspartic acid receptor (NMDAR) dysregulation has been strongly associated with the pathophysiology of mental ill eight subtypes (1), are potential novel tar- gets for neuropsychiatric disorders (24). Group I mGluR (m

  16. High-energy mechanical milling of poly(methyl methacrylate), polyisoprene and poly(ethylene-alt-propylene)

    E-Print Network [OSTI]

    High-energy mechanical milling of poly(methyl methacrylate), polyisoprene and poly(ethylene-alt-propylene(methyl methacrylate) (PMMA) at ambient and cryogenic temperatures, as well as on polyisoprene (PI) and poly(ethylene-alt-propylene

  17. Methyl-CpG island-associated genome signature tags

    DOE Patents [OSTI]

    Dunn, John J

    2014-05-20T23:59:59.000Z

    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.

  18. Ethanol Demand in United States Production of Oxygenate-limited Gasoline

    SciTech Connect (OSTI)

    Hadder, G.R.

    2000-08-16T23:59:59.000Z

    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.

  19. Personal Services Agreements Waivers

    E-Print Network [OSTI]

    , State Controller's Office). All personal services contract activity will be reported through the state

  20. Personal Services Agreements Waivers

    E-Print Network [OSTI]

    . Type of Service 1. Consultant Services: Include consulting services, program evaluators, standards, or the School does not have the equipment necessary to perform these services. 6. Graphic and Journalistic Service: Services including graphic design, writing and editing and bookbinding for which CSM does

  1. Personal Services Agreements Waivers

    E-Print Network [OSTI]

    these services. 4. Support and Maintenance Agreements: Services include preventive maintenance as well - Equipment Maintenance/Repair Services in this category are used for all types of equipment maintenance the equipment necessary to perform certain services. 2. Equipment Maintenance and Repair: Services include

  2. Composition of the wax fraction of bitumen from methylated brown coals

    SciTech Connect (OSTI)

    S.I. Zherebtsov; A.I. Moiseev [Russian Academy of Sciences, Kemerovo (Russian Federation). Institute of Coal and Coal Chemistry

    2009-04-15T23:59:59.000Z

    Changes in the group and individual compositions of the wax fractions of bitumen in the course of brown coal methylation were studied. With the use of IR and NMR spectroscopy and chromatography-mass spectrometry, it was found that the esters of methylated coal waxes consisted of the native esters of fatty acids and the methyl esters of these acids formed as a result of an alkylation treatment. Esterification and transesterification were predominant among the reactions of aliphatic fraction components. A positive effect of methanol alkylation on an increase in the yield of the aliphatic fractions was found.

  3. Anti-inflammatory and antifibrotic effects of methyl palmitate

    SciTech Connect (OSTI)

    El-Demerdash, Ebtehal, E-mail: ebtehal_dm@yahoo.com

    2011-08-01T23:59:59.000Z

    Methyl palmitate (MP) has been shown earlier to inhibit Kupffer cells and rat peritoneal macrophages. To evaluate the potential of MP to inhibit the activation of other macrophages, RAW cells (macrophages of alveolar origin) were treated with varying concentrations of MP (0.25, 0.5, 1 mM). Assessment of cytotoxicity using MTT assay revealed that 0.25 and 0.5 mM are not toxic to RAW cells. MP was able to inhibit the phagocytic function of RAW cells. Treatment of cells with MP 24 hours prior to LPS stimulation significantly decreased nitric oxide release and altered the pattern of cytokines release; there was a significant decrease in TNF-{alpha} and a significant increase in IL-10 compared to the controls. However, there is a non-significant change in IL-6 level. Furthermore, phosphorylation of inhibitory kappa B (I{kappa}B{alpha}) protein was significantly decreased in RAW cells treated with 0.5 mM MP after LPS stimulation. Based upon the in-vitro results, it was examined whether MP treatment will be effective in preventing bleomycin-induced lung inflammation and fibrosis in-vivo. Bleomycin given by itself caused destruction of the lung architecture characterized by pulmonary fibrosis with collapse of air alveoli and emphysematous. Bleomycin induced a significant increase in hydroxyproline level and activated NF-{kappa}B, p65 expression in the lung. MP co-treatment significantly ameliorated bleomycin effects. These results suggest that MP has a potential of inhibiting macrophages in general. The present study demonstrated for the first time that MP has anti-inflammatory and antifibrotic effect that could be through NF-kB inhibition. Thus MP like molecule could be a promising anti-inflammatory and antifibrotic drug. - Research Highlights: >Methyl palmitate is a universal macrophage inhibitor. >It could be a promising nucleus of anti-inflammatory and antifibrotic drugs. >The underlying mechanism of these effects could be through NF-kB inhibition.

  4. 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

    1999-07-19T23:59:59.000Z

    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.

  5. Methyl jasmonate elicits rapid changes in carbon and nitrogen dynamics in tomato

    E-Print Network [OSTI]

    Orians, Colin

    Methyl jasmonate elicits rapid changes in carbon and nitrogen dynamics in tomato Sara Gomez1 of Biological Sciences, University of Rhode Island, Kingston, RI, USA Author for correspondence: Sara Gomez Tel

  6. Halogenated 1'-methyl-1,2'-bipyrroles (MBPs) in the Norwestern Atlantic

    E-Print Network [OSTI]

    Pangallo, Kristin C

    2009-01-01T23:59:59.000Z

    Halogenated 1'-methyl-1,2'-bipyrroles (MBPs) are a distinctive class of marine organic compounds. They are naturally produced, they have a unique carbon structure, they are highly halogenated, and they bioaccumulate in ...

  7. Thermomechanical properties of polyhedral oligomeric silsequioxane- poly(methyl methacrylate) nanocomposites

    E-Print Network [OSTI]

    Kopesky, Edward Thomas

    2005-01-01T23:59:59.000Z

    Poly(methyl methacrylate)s (PMMA) containing polyhedral oligomeric silsesquioxane (POSS) nanoparticles (d [approx.] 1.5 nm) were subjected to heological, mechanical, and morphological tests to determine the effects that ...

  8. A unique regulatory phase of DNA methylation in the early mammalian embryo

    E-Print Network [OSTI]

    Chan, Michelle M.

    DNA methylation is highly dynamic during mammalian embryogenesis. It is broadly accepted that the paternal genome is actively depleted of 5-methylcytosine at fertilization, followed by passive loss that reaches a minimum ...

  9. Cryogenic Mechanical Alloying of Poly(methyl methacrylate) with Polyisoprene and Poly(ethylene-alt-propylene)

    E-Print Network [OSTI]

    Cryogenic Mechanical Alloying of Poly(methyl methacrylate) with Polyisoprene and Poly(ethylene-alt-propylene temperatures to incorporate polyisoprene (PI) or its hydrogenated analogue poly(ethylene-alt-propylene) (PEP

  10. E-Print Network 3.0 - atropine methyl bromide Sample Search Results

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

    methyl nitrate, Sigma-Aldrich, 05 mg kg bolus, followed by 025 mg kg h infusion i... -Aldrich), 5 mg kg bolus i.v. followed by 5 mg kg h continuous infusion...

  11. Selective Monoarylation of Acetate Esters and Aryl Methyl Ketones Using Aryl Chlorides

    E-Print Network [OSTI]

    Biscoe, Mark R.

    Simple, efficient procedures for the monoarylation of acetate esters and aryl methyl ketones using aryl chlorides are presented. Previously, no general method was available to ensure the highly selective monoarylation of ...

  12. Heavy-atom isotope effects on the acid-catalyzed hydrolysis of methyl benzoate

    SciTech Connect (OSTI)

    Marlier, J.F.; O'Leary, M.H.

    1981-05-08T23:59:59.000Z

    Results of the use of a previously reported technique of four-heavy atom isotope effects for study of the acid-catalyzed hydrolysis of methyl benzoate are reported. Ether oxygen and methyl carbon isotope effects on the reaction were measured by the usual natural-abundance isotope-ratio technique. The carbonyl oxygen isotope effect was measured by the pseudo-natural-abundance double-label method as was the carbonyl carbon isotope effect. The results led to the assumption that the hydrolysis of methyl benzoate proceeds by way of a tetrahedral intermediate. The small amount of oxygen exchange with the solvent that accompanies the hydrolysis indicated that it is intermediate formation rather than decomposition that is rate determining. The small magnitude of the observed carbon isotope effect on the acid-catalyzed hydrolysis of methyl benzoate compared to carbon isotope effects on other reactions of this compound indicate that the transition state is relatively reactant-like. (BLM)

  13. Chromosome-wide mapping of DNA methylation patterns in normal and malignant prostate cells reveals pervasive methylation of gene-associated and conserved intergenic sequences

    E-Print Network [OSTI]

    Yegnasubramanian, Srinivasan; Wu, Zhijin; Haffner, Michael C; Esopi, David; Aryee, Martin J; Badrinath, Raghav; He, Tony L; Morgan, James D; Carvalho, Benilton S; Zheng, Qizhi; De Marzo, Angelo M; Irizarry, Rafael A; Nelson, William G

    2011-06-13T23:59:59.000Z

    G island [13-15], chromosome-wide [15], or genome-wide [16] til- ing microarrays or to analyze by next generation sequen- cing [17,18]. Here, we describe the use of an MBD-chip approach (Figure 1A) to compare the chromosome-wide DNA methylation patterns... identified as differentially methylated in the LNCaP cells compared to the PrEC cells. We could then compare the distribution of CpG dinucleotide content and number of regions overlapping CpG islands in these simulated data sets with these parameters in our...

  14. Radio-methyl vorozole and methods for making and using the same

    DOE Patents [OSTI]

    Kim, Sung Won; Biegon, Anat; Fowler, Joanna S.

    2014-08-05T23:59:59.000Z

    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.

  15. Radio-methyl vorozole and methods for making and using the same

    DOE Patents [OSTI]

    Kim, Sung Won; Biegon, Anat; Fowler, Joanna S.

    2014-08-12T23:59:59.000Z

    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.

  16. Vapor-liquid equilibria of hydrocarbons and fuel oxygenates. 2

    SciTech Connect (OSTI)

    Bennett, A.; Lamm, S.; Orbey, H.; Sandler, S.I. (Univ. of Delaware, Newark (United States))

    1993-04-01T23:59:59.000Z

    Vapor-liquid equilibrium data for methyl tert-butyl ether (MTBE) + 1-heptene, MTBE + four-component gasoline prototype, ethanol + four-component gasoline prototype, and separately MTBE and ethanol with the Auto/Oil Air Quality Improvement Research Gasoline Blend A are reported. Small additions of MTBE have a very small effect on the total equilibrium pressure of this gasoline blend, and at most temperatures will decrease this pressure. In contrast, small additions of ethanol to this gasoline blend result in a significant increase in the equilibrium pressure at all temperatures. Analysis shows that the vapor-liquid equilibrium data for the MTBE-containing systems are easily correlated using a modified Peng-Robinson equation of state with conventional van der Waals one-fluid mixing rules. Data for mixtures containing ethanol cannot be accurately correlated in this way.

  17. INVOLVED IN DE NOVO 2-containing complex involved in RNA-directed DNA methylation in Arabidopsis

    SciTech Connect (OSTI)

    Ausin, Israel; Greenberg, Maxim V.C.; Simanshu, Dhirendra K.; Hale, Christopher J.; Vashisht, Ajay A.; Simon, Stacey A.; Lee, Tzuu-fen; Feng, Suhua; Espaola, Sophia D.; Meyers, Blake C.; Wohlschlegel, James A.; Patel, Dinshaw J.; Jacobsen, Steven E. (UCLA); (MSKCC); (Delaware)

    2012-10-23T23:59:59.000Z

    At least three pathways control maintenance of DNA cytosine methylation in Arabidopsis thaliana. However, the RNA-directed DNA methylation (RdDM) pathway is solely responsible for establishment of this silencing mark. We previously described INVOLVED IN DE NOVO 2 (IDN2) as being an RNA-binding RdDM component that is required for DNA methylation establishment. In this study, we describe the discovery of two partially redundant proteins that are paralogous to IDN2 and that form a stable complex with IDN2 in vivo. Null mutations in both genes, termed IDN2-LIKE 1 and IDN2-LIKE 2 (IDNL1 and IDNL2), result in a phenotype that mirrors, but does not further enhance, the idn2 mutant phenotype. Genetic analysis suggests that this complex acts in a step in the downstream portion of the RdDM pathway. We also have performed structural analysis showing that the IDN2 XS domain adopts an RNA recognition motif (RRM) fold. Finally, genome-wide DNA methylation and expression analysis confirms the placement of the IDN proteins in an RdDM pathway that affects DNA methylation and transcriptional control at many sites in the genome. Results from this study identify and describe two unique components of the RdDM machinery, adding to our understanding of DNA methylation control in the Arabidopsis genome.

  18. Technical and operational overview of the C[sub 4] Oleflex process at Valero refinery

    SciTech Connect (OSTI)

    Hohnholt, J.F.; Payne, D. (Valero Refining Co., Corpus Christi, TX (United States)); Gregor, J.; Smith, E. (UOP, Des Plaines, IL (United States))

    1994-01-01T23:59:59.000Z

    Changes in gasoline composition stemming from the 1990 Clean Air Act (CAA) Amendments prompted Valero Energy Corporation to evaluate options for producing reformulated gasoline. The evaluation culminated in a project to upgrade butanes into methyl tertiary butyl ether (MTBE). Technology selection focused on the dehydrogenation of isobutane, and the UOP Oleflex process was selected. The MTBE project was implemented in 34 months and was $3 million under budget. The guaranteed MTBE production of 12,500 BPSD was achieved within one month of mechanical completion and has since reached 15,000 BPSD. Even at the low MTBE prices prevailing in late 1993, the butane upgrading project contributed significantly to Valero Refinery's overall profitability. Worldwide demand is expected to increase MTBE prices in 1996, thereby further increasing profits. The paper describes the project evaluation activities which led to the selection of the Oleflex process, engineering and construction, the MTBE complex start-up and operation, the Valero MTBE complex performance, and future plans. The paper also discusses feedstock utilization efficiency and MTBE market analysis.

  19. Polystyrene/Poly(methyl methacrylate) Blends in the Presence of Cyclohexane: Selective Solvent Washing or Equilibrium Adsorption?

    E-Print Network [OSTI]

    -cyclohexane (PS:CH), poly(methyl methacrylate)-carbon tetrachloride (PMMA:CCl4), and PS:CCl4 adsorbing

  20. Austrian refiner benefits from advanced control

    SciTech Connect (OSTI)

    Richard, L.A.; Spencer, M. [Setpoint Inc., Houston, TX (United States); Schuster, R.; Tuppinger, D.M.; Wilmsen, W.F. [OeMV-AG Energy, Schwechat (Austria)

    1995-03-20T23:59:59.000Z

    OeMV-AG Energy implemented advanced process controls on 27 units at its refinery in Schwechat, Austria. A variety of controls were implemented on the butadiene and methyl tertiary butyl ether (MTBE) units in January 1993. After more than 1 year of operation, the butadiene/MTBE project has shown a number of benefits, including reduced energy consumption and increased capacity in both units. The paper discusses the process, advanced control, the simple model predictive controller, control objectives, the butadiene unit, the MTBE unit, and benefits of the advanced controllers.

  1. Biogeochemistry of arsenic in natural waters: The importance of methylated species

    SciTech Connect (OSTI)

    Anderson, L.C.D.; Bruland, K.W. (Univ. of California, Santa Cruz (USA))

    1991-03-01T23:59:59.000Z

    Water samples from a number of lakes and estuaries, mostly in California, showed measurable concentrations of methylated arsenic (equivalent to 1-59% of total As) with the exception of one highly alkaline lake. Neither depleted phosphate concentrations nor high dissolved salts correlated with the appearance of methylated forms of As. A temporal study of As speciation in Davis Creek Reservoir, a seasonally anoxic lake in northern California, demonstrated that dimethylarsinic acid increased sufficiently to become the dominant form of dissolved As within the surface photic zone during late summer and fall. Methylated forms decreased while arsenate increased when the lake over-turned in early December, which suggested a degradation of dimethylarsinic acid to arsenate.

  2. Synthesis Of [2h, 13c] And [2h3, 13c]Methyl Aryl Sulfides

    DOE Patents [OSTI]

    Martinez, Rodolfo A. (Santa Fe, NM); Alvarez, Marc A. (Santa Fe, NM); Silks, III, Louis A. (Los Alamos, NM); Unkefer, Clifford J. (Los Alamos, NM)

    2004-03-30T23:59:59.000Z

    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.

  3. 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, E-mail: yizc@buaa.edu.cn

    2012-11-15T23:59:59.000Z

    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.

  4. 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.

    1994-06-01T23:59:59.000Z

    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.

  5. Kinetics of the reduction of methyl viologen with hydrogen on a colloidal Pt catalyst

    SciTech Connect (OSTI)

    Maier, V.E.; Shafirovich, V.Ya.

    1988-10-01T23:59:59.000Z

    The evolution of H/sub 2/ on a Pt catalyst under the influence of one-electron reductors is part of the photocatalytic process of decomposition of H/sub 2/O into H/sub 2/ and O/sub 2/. As a model reaction we selected the reduction of methyl viologen. The bonding constant for hydrogen on colloidal Pt, as well as the effective rate constant of the heterolytic splitting of H/sub 2/ on the same Pt catalyst are determined. A mathematical description of the reduction of methyl viologen with hydrogen is suggested.

  6. Salt effect on the isobaric vapor-liquid equilibrium of the methyl acetate + methanol system

    SciTech Connect (OSTI)

    Iliuta, M.C.; Thyrion, F.C. [Louvain Univ., Louvain-la-Neuve (Belgium). Chemical Engineering Inst.] [Louvain Univ., Louvain-la-Neuve (Belgium). Chemical Engineering Inst.; Landauer, O.M. [Univ. Politehnica Bucharest (Romania)] [Univ. Politehnica Bucharest (Romania)

    1996-07-01T23:59:59.000Z

    The effect of sodium thiocyanate at constant salt mole fraction from 0.01 to 0.05 and at saturation on the vapor-liquid equilibrium (VLE) of methyl acetate + methanol has been studied at 101.32 kPa using a modified Othmer equilibrium still. The salt exhibited both salting-in and salting-out effects on the methyl acetate, the azeotrope being eliminated at saturation. The results were correlated using the extended UNIQUAC model of Sander et al. and the electrolytic NRTL model of Mock et al.

  7. Ab initio study of thiol aqueous phase ionization energies. Methyl mercaptan and cysteamine

    SciTech Connect (OSTI)

    Colson, A.O.; Sevilla, M.D. (Oakland Univ., Rochester, MI (United States))

    1994-10-13T23:59:59.000Z

    The ionization energies of two thiol model compounds (methyl mercaptan and cysteamine) are calculated at the ROHF/6-31G* level to aid our understanding of the mechanisms involved in DNA radioprotection. Methyl mercaptan, the thiolate anion, and its trihydrated form are fully geometry optimized. The resulting gas-phase Koopmans ionization energies are 9.68, 1.67, and 3.63 eV, respectively. The ionization energy for the solvated methylthiolate anion, CH[sub 3]S[sup [minus

  8. Putative Zinc Finger Protein Binding Sites Are Over-Represented in the Boundaries of Methylation-Resistant

    E-Print Network [OSTI]

    Putative Zinc Finger Protein Binding Sites Are Over- Represented in the Boundaries of Methylation that there are several over-represented putative Transcription Factor Binding Sites (TFBSs) in methylation-resistant CpG islands, and a specific group of zinc finger protein binding sites are over-represented in boundary

  9. Histidine methylation of yeast ribosomal protein Rpl3p is1 required for proper 60S subunit assembly2

    E-Print Network [OSTI]

    Clarke, Steven

    -site. Rpl3p methylation is dependent upon the presence of Hpm1p, a24 candidate seven beta strand methyltransferase. In this study, we elucidated the biological activities of25 Hpm1p in vitro and in vivo. Amino acid analyses reveal that Hpm1p is responsible for all detectable26 protein histidine methylation

  10. Infrared Study of the Molecular Orientation in Ultrathin Films of Behenic Acid Methyl Ester: Comparison between

    E-Print Network [OSTI]

    Pezolet, Michel

    Infrared Study of the Molecular Orientation in Ultrathin Films of Behenic Acid Methyl Ester-Blodgett transfer. The presence in the infrared spectra of several bands due to the methylene wagging and twisting and infrared spectroscopy have been developed to study these films. Infrared spectroscopy is particularly

  11. Active transport, substrate specificity, and methylation of Hg(II) in anaerobic bacteria

    SciTech Connect (OSTI)

    Schasfer, Jeffra [Princeton University; Rocks, Sara [Princeton University; Zheng, Wang [ORNL; Liang, Liyuan [ORNL; Gu, Baohua [ORNL; Morel, Francois M [ORNL

    2011-01-01T23:59:59.000Z

    The formation of methylmercury (MeHg), which is biomagnified in aquatic food chains and poses a risk to human health, is effected by some iron- and sulfate-reducing bacteria (FeRB and SRB) in anaerobic environments. However, very little is known regarding the mechanism of uptake of inorganic Hg by these organisms, in part because of the inherent difficulty in measuring the intracellular Hg concentration. By using the FeRB Geobacter sulfurreducens and the SRB Desulfovibrio desulfuricans ND132 as model organisms, we demonstrate that Hg(II) uptake occurs by active transport. We also establish that Hg(II) uptake by G. sulfurreducens is highly dependent on the characteristics of the thiols that bind Hg(II) in the external medium, with some thiols promoting uptake and methylation and others inhibiting both. The Hg(II) uptake system of D. desulfuricans has a higher affinity than that of G. sulfurreducens and promotes Hg methylation in the presence of stronger complexing thiols. We observed a tight coupling between Hg methylation and MeHg export from the cell, suggesting that these two processes may serve to avoid the build up and toxicity of cellular Hg. Our results bring up the question of whether cellular Hg uptake is specific for Hg(II) or accidental, occurring via some essential metal importer. Our data also point at Hg(II) complexation by thiols as an important factor controlling Hg methylation in anaerobic environments.

  12. Biodegradation of triclosan and formation of methyl-triclosan in activated sludge under aerobic conditions

    E-Print Network [OSTI]

    Kolaei, Alireza Rezania

    Biodegradation of triclosan and formation of methyl-triclosan in activated sludge under aerobic in activated sludge from a standard activated sludge WWTP equipped with enhanced biological phosphorus removal) and anaerobic conditions rather low removal rates were determined. In a laboratory-scale activated sludge

  13. Growth of diamond films using an enclosed methyl-acetylene and propadiene combustion flame

    E-Print Network [OSTI]

    Dandy, David

    1 Growth of diamond films using an enclosed methyl-acetylene and propadiene combustion flame K Abstract Diamond growth in low pressure combustion flames was studied using a safer, more economical and chemical kinetic time scales in the combustion reactor. 1 Present Address: 3M Corporation, Bldg. 60-1N-01

  14. On the spherically symmetrical combustion of methyl decanoate droplets and comparisons with detailed numerical modeling

    E-Print Network [OSTI]

    Walter, M.Todd

    .53­0.57 mm and the combustion gas is normal atmospheric pressure air. A detailed numerical simulationOn the spherically symmetrical combustion of methyl decanoate droplets and comparisons Biodiesel Biofuel Microgravity Numerical Droplet combustion a b s t r a c t This study presents

  15. Neutralization of Methyl Cation via Chemical Reactions in Low-Energy Ion-Surface

    E-Print Network [OSTI]

    Wysocki, Vicki H.

    with Fluorocarbon and Hydrocarbon Self-Assembled Monolayer Films A´ rpa´d Somogyi, Darrin L. Smith, and Vicki H-surface collisions of methyl cation at hydrocarbon and fluorocarbon self- assembled monolayer (SAM) surfaces produce with hydrocarbon and fluorocarbon SAMs occurs by concerted chemical reactions, i.e., that neutralization

  16. Enhanced diisobutene production in the presence of methyl tertiary butyl ether

    DOE Patents [OSTI]

    Smith, L.A. Jr.

    1983-03-01T23:59:59.000Z

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

    E-Print Network [OSTI]

    Wan, Xin-hua

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

  18. Polymer surface and thin film vibrational dynamics of poly,,methyl methacrylate..., polybutadiene,

    E-Print Network [OSTI]

    Sibener, Steven

    Polymer surface and thin film vibrational dynamics of poly,,methyl methacrylate..., polybutadiene atom scattering has been used to investigate the vibrational dynamics at the polymer vacuum interface polymers. The broad multiphonon feature that arises in the inelastic scattering spectra at surface

  19. Hybrid Energy Cell for Degradation of Methyl Orange by Self-Powered Electrocatalytic Oxidation

    E-Print Network [OSTI]

    Wang, Zhong L.

    Hybrid Energy Cell for Degradation of Methyl Orange by Self- Powered Electrocatalytic Oxidation Ya of superoxidative hydroxyl radical on the anode. Here, we report a hybrid energy cell that is used for a self-powered electrocatalytic process for the degradation of MO without using an external power source. The hybrid energy cell

  20. Sequential 2 -O-Methylation of Archaeal Pre-tRNATrp Nucleotides

    E-Print Network [OSTI]

    Maxwell, E. Stuart

    Sequential 2 -O-Methylation of Archaeal Pre-tRNATrp Nucleotides Is Guided by the Intron -O-methyla- tion of nucleotides C34 and U39 followed by intron exci- sion. Positioning of the box C proteins. With both kinetic studies and single nucleotide substitutions of target and guide nucleotides, we