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Journal articles on the topic 'Butyl methyl ether In situ bioremediation'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Hristova, Krassimira R., Christian M. Lutenegger, and Kate M. Scow. "Detection and Quantification of Methyl tert-Butyl Ether-Degrading Strain PM1 by Real-Time TaqMan PCR." Applied and Environmental Microbiology 67, no. 11 (2001): 5154–60. http://dx.doi.org/10.1128/aem.67.11.5154-5160.2001.

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ABSTRACT The fuel oxygenate methyl tert-butyl ether (MTBE), a widely distributed groundwater contaminant, shows potential for treatment by in situ bioremediation. The bacterial strain PM1 rapidly mineralizes and grows on MTBE in laboratory cultures and can degrade the contaminant when inoculated into groundwater or soil microcosms. We applied the TaqMan quantitative PCR method to detect and quantify strain PM1 in laboratory and field samples. Specific primers and probes were designed for the 16S ribosomal DNA region, and specificity of the primers was confirmed with DNA from 15 related bacteri

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2

d’Errico, Giada, Veronica Aloj, Valeria Ventorino, et al. "Methyl t-butyl ether-degrading bacteria for bioremediation and biocontrol purposes." PLOS ONE 15, no. 2 (2020): e0228936. http://dx.doi.org/10.1371/journal.pone.0228936.

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3

Hu, C., K. Acuna-Askar, and A. J. Englande. "Bioremediation of methyl tertiary-butyl ether (MTBE) by an innovative biofilter." Water Science and Technology 49, no. 1 (2004): 87–94. http://dx.doi.org/10.2166/wst.2004.0026.

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Methyl tertiary-butyl ether (MTBE) is a synthetic chemical used in unleaded gasoline as an additive to reduce levels of ozone and carbon monoxide from auto exhaust. Due to its chemical and recalcitrant properties, MTBE has caused groundwater contamination worldwide. A laboratory-scale biofilter made of a natural fiber (kenaf) mat and inoculated with MTBE-degrading microorganisms, was evaluated for MTBE removal efficiency. Operational parameters of oxygen flow rate, hydraulic retention time (HRT), yeast extract and initial MTBE concentration were varied and MTBE removal efficiencies determined.

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4

Lalevic, Blazo, Jelena Jovic, Vera Raicevic, Igor Kljujev, Dragan Kikovic, and Saud Hamidovic. "Biodegradation of methyl tert-butyl ether by Kocuria sp." Chemical Industry 66, no. 5 (2012): 717–22. http://dx.doi.org/10.2298/hemind120110019l.

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Methyl tert-butyl ether (MTBE) has been used to replace the toxic compounds from gasoline and to reduce emission of air pollutants. Due to its intensive use, MTBE has become one of the most important environment pollutants. The aim of this paper is isolation and identification of the bacteria from wastewater sample of ?HIP Petrohemija? Pancevo (Serbia), capable of MTBE biodegradation. The results of the investigation showed that only the bacterial isolate 27/1 was capable of growth on MTBE. The result of sequence analyzes of 16S rDNA showed that this bacterial isolate belongs to the Kocuria sp

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5

Guisado, I. M., J. Purswani, L. Catón-Alcubierre, J. González-López, and C. Pozo. "Toxicity and biofilm-based selection for methyl tert-butyl ether bioremediation technology." Water Science and Technology 74, no. 12 (2016): 2889–97. http://dx.doi.org/10.2166/wst.2016.461.

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Extractive membrane biofilm reactor (EMBFR) technology offers productive solutions for volatile and semi-volatile compound removal from water bodies. In this study, the bacterial strains Paenibacillus etheri SH7T (CECT 8558), Agrobacterium sp. MS2 (CECT 8557) and Rhodococcus ruber strains A5 (CECT 8556), EE6 (CECT 8612) and EE1 (CECT 8555), previously isolated from fuel-contaminated sites, were tested for adherence on tubular semipermeable membranes in laboratory-scale systems designed for methyl tert-butyl ether (MTBE) bioremediation. Biofilm formation on the membrane surface was evaluated th

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6

Yousefi, Zabihollah, Zeinab Tahernezhad, Seyed Noroddin Mousavinasab, Reza Safari, and Ahmadreza Bekhradnia. "Bioremediation of methyl tertiary-butyl ether (MTBE) by three pure bacterial cultures." Environmental Health Engineering and Management 5, no. 2 (2018): 123–28. http://dx.doi.org/10.15171/ehem.2018.17.

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7

Chen, Colin S., Chien-Jun Tien, and Kai-Van Zhan. "Evaluation of Intrinsic Bioremediation of Methyl Tert-butyl Ether (MTBE) Contaminated Groundwater." Journal of Soil and Groundwater Environment 19, no. 5 (2014): 9–17. http://dx.doi.org/10.7857/jsge.2014.19.5.009.

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8

Volpe, Angela, Guido Del Moro, Simona Rossetti, Valter Tandoi, and Antonio Lopez. "Enhanced bioremediation of methyl tert-butyl ether (MTBE) by microbial consortia obtained from contaminated aquifer material." Chemosphere 75, no. 2 (2009): 149–55. http://dx.doi.org/10.1016/j.chemosphere.2008.12.053.

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9

Matusiak, Grazyna. "1,3-Dipolar Cycloaddition Reactions of the Ylide Derived from 6-Phenacyl-benzo[f][1,7]naphthyridinium Bromide." Australian Journal of Chemistry 52, no. 2 (1999): 149. http://dx.doi.org/10.1071/c98109.

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The 1,3-dipolar cycloaddition reactions of 4,6-diazaphenanthrene 6-phenacylide formed in situ from the quaternary 6-phenacylbenzo[f][1,7]naphthyridinium bromide in basic medium were examined; methacrylic acid, methyl methacrylate, butyl vinyl ether, methyl vinyl ketone, maleic anhydride and dimethyl acetylenedicarboxylate were used as the dipolarophiles.

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10

Haas, Joseph E., and Donald A. Trego. "A Field Application of Hydrogen-Releasing Compound (HRCTM) for the Enhanced Bioremediation of Methyl Tertiary Butyl Ether (MTBE)." Soil and Sediment Contamination: An International Journal 10, no. 5 (2001): 555–75. http://dx.doi.org/10.1080/20015891109437.

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11

Guisado, I. M., J. Purswani, J. Gonzalez-Lopez, and C. Pozo. "Physiological and genetic screening methods for the isolation of methyl tert-butyl ether-degrading bacteria for bioremediation purposes." International Biodeterioration & Biodegradation 97 (January 2015): 67–74. http://dx.doi.org/10.1016/j.ibiod.2014.11.008.

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12

Nikpay, A., H. Kazemian, and M. Sadeghi. "Remediation of Methyl Tert-Butyl Ether Contaminated Water by Using In situ Catalytic and Biological Combined Techniques." American Journal of Environmental Sciences 4, no. 6 (2008): 710–15. http://dx.doi.org/10.3844/ajessp.2008.710.715.

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13

Kane, S. R., H. R. Beller, T. C. Legler, et al. "Aerobic Biodegradation of Methyltert-Butyl Ether by Aquifer Bacteria from Leaking Underground Storage Tank Sites." Applied and Environmental Microbiology 67, no. 12 (2001): 5824–29. http://dx.doi.org/10.1128/aem.67.12.5824-5829.2001.

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ABSTRACT The potential for aerobic methyl tert-butyl ether (MTBE) degradation was investigated with microcosms containing aquifer sediment and groundwater from four MTBE-contaminated sites characterized by oxygen-limited in situ conditions. MTBE depletion was observed for sediments from two sites (e.g., 4.5 mg/liter degraded in 15 days after a 4-day lag period), whereas no consumption of MTBE was observed for sediments from the other sites after 75 days. For sediments in which MTBE was consumed, 43 to 54% of added [U-14C]MTBE was mineralized to14CO2. Molecular phylogenetic analyses of these se

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14

Hunger, M., T. Horvath, and J. Weitkamp. "Methyl tertiary-butyl ether synthesis on zeolite HBeta investigated by in situ MAS NMR spectroscopy under continuous-flow conditions." Microporous and Mesoporous Materials 22, no. 1-3 (1998): 357–67. http://dx.doi.org/10.1016/s1387-1811(98)00078-x.

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15

Hristova, Krassimira, Binyam Gebreyesus, Douglas Mackay, and Kate M. Scow. "Naturally Occurring Bacteria Similar to the Methyl tert-Butyl Ether (MTBE)-Degrading Strain PM1 Are Present in MTBE-Contaminated Groundwater." Applied and Environmental Microbiology 69, no. 5 (2003): 2616–23. http://dx.doi.org/10.1128/aem.69.5.2616-2623.2003.

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ABSTRACT Methyl tert-butyl ether (MTBE) is a widespread groundwater contaminant that does not respond well to conventional treatment technologies. Growing evidence indicates that microbial communities indigenous to groundwater can degrade MTBE under aerobic and anaerobic conditions. Although pure cultures of microorganisms able to degrade or cometabolize MTBE have been reported, to date the specific organisms responsible for MTBE degradation in various field studies have not be identified. We report that DNA sequences almost identical (99% homology) to those of strain PM1, originally isolated

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16

Rodeghero, Elisa, Luisa Pasti, Elena Sarti, Giuseppe Cruciani, Roberto Bagatin, and Annalisa Martucci. "Temperature-Induced Desorption of Methyl tert-Butyl Ether Confined on ZSM-5: An In Situ Synchrotron XRD Powder Diffraction Study." Minerals 7, no. 3 (2017): 34. http://dx.doi.org/10.3390/min7030034.

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17

Somsamak, Piyapawn, Hans H. Richnow, and Max M. Häggblom. "Carbon Isotope Fractionation during Anaerobic Degradation of Methyl tert-Butyl Ether under Sulfate-Reducing and Methanogenic Conditions." Applied and Environmental Microbiology 72, no. 2 (2006): 1157–63. http://dx.doi.org/10.1128/aem.72.2.1157-1163.2006.

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ABSTRACT Methyl tert-butyl ether (MTBE), an octane enhancer and a fuel oxygenate in reformulated gasoline, has received increasing public attention after it was detected as a major contaminant of water resources. Although several techniques have been developed to remediate MTBE-contaminated sites, the fate of MTBE is mainly dependent upon natural degradation processes. Compound-specific stable isotope analysis has been proposed as a tool to distinguish the loss of MTBE due to biodegradation from other physical processes. Although MTBE is highly recalcitrant, anaerobic degradation has been demo

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18

Saponaro, Sabrina, Marco Negri, Elena Sezenna, Luca Bonomo, and Claudia Sorlini. "Groundwater remediation by an in situ biobarrier: A bench scale feasibility test for methyl tert-butyl ether and other gasoline compounds." Journal of Hazardous Materials 167, no. 1-3 (2009): 545–52. http://dx.doi.org/10.1016/j.jhazmat.2009.01.026.

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19

Shi, Weijia, and Gang Zou. "Palladium-Catalyzed Room Temperature Acylative Cross-Coupling of Activated Amides with Trialkylboranes." Molecules 23, no. 10 (2018): 2412. http://dx.doi.org/10.3390/molecules23102412.

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A highly efficient acylative cross-coupling of trialkylboranes with activated amides has been effected at room temperature to give the corresponding alkyl ketones in good to excellent yields by using 1,3-bis(2,6-diisopropyl)phenylimidazolylidene and 3-chloropyridine co-supported palladium chloride, the PEPPSI catalyst, in the presence of K2CO3 in methyl tert-butyl ether. The scope and limitations of the protocol were investigated, showing good tolerance of acyl, cyano, and ester functional groups in the amide counterpart while halo group competed via the classical Suzuki coupling. The trialkyl

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20

Pongkua, Waleeporn, Rujira Dolphen, and Paitip Thiravetyan. "Bioremediation of gaseous methyl tert-butyl ether by combination of sulfuric acid modified bagasse activated carbon-bone biochar beads and Acinetobacter indicus screened from petroleum contaminated soil." Chemosphere 239 (January 2020): 124724. http://dx.doi.org/10.1016/j.chemosphere.2019.124724.

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21

Hosseini, Mehdi, and Nasser Dalali. "Use of Ionic Liquids for Trace Analysis of Methyl Tert-Butyl Ether in Water Samples using in situ Solvent Formation Microextraction Technique and Determination by GC/FID." Separation Science and Technology 49, no. 12 (2014): 1889–94. http://dx.doi.org/10.1080/01496395.2014.894524.

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22

Talvenmäki, Harri, Niina Lallukka, Suvi Survo, and Martin Romantschuk. "Fenton’s reaction-based chemical oxidation in suboptimal conditions can lead to mobilization of oil hydrocarbons but also contribute to the total removal of volatile compounds." Environmental Science and Pollution Research 26, no. 33 (2019): 34670–84. http://dx.doi.org/10.1007/s11356-019-06547-3.

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Abstract Fenton’s reaction-based chemical oxidation is in principle a method that can be utilized for all organic fuel residues thus making it a potential all-purpose, multi-contaminant, in situ application for cases in which storage and distribution of different types of fuels have resulted in contamination of soil or groundwater. Since peroxide breakdown reactions are also expected to lead to a physical transport of the target compound, this secondary physical removal, or rebound concentrations related to it, is prone to be affected by the chemical properties of the target compound. Also, si

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23

Alpmann, Alexander, and Gertrud Morlock. "Rapid and Cost-Effective Determination of Acrylamide in Coffee by Planar Chromatography and Fluorescence Detection After Derivatization with Dansulfinic Acid." Journal of AOAC INTERNATIONAL 92, no. 3 (2009): 725–29. http://dx.doi.org/10.1093/jaoac/92.3.725.

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Abstract A new method has been developed for the determination of acrylamide in ground coffee by planar chromatography using prechromatographic in situ derivatization with dansulfinic acid. After pressurized fluid extraction of acrylamide from the coffee samples, the extracts were passed through activated carbon and concentrated. These extracts were applied onto a silica gel 60 HPTLC plate and oversprayed with dansulfinic acid. By heating the plate, acrylamide was derivatized into the fluorescent product dansylpropanamide. The chromatographic separation with ethyl acetatetert.-butyl methyl eth

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24

Horvath, Thomas, Michael Seiler, and Michael Hunger. "A comparative study of methyl-tert-butyl ether synthesis on zeolites HY, HBeta, HBeta/F and HZSM-5 by in situ MAS NMR spectroscopy under flow conditions and on-line gas chromatography." Applied Catalysis A: General 193, no. 1-2 (2000): 227–36. http://dx.doi.org/10.1016/s0926-860x(99)00432-9.

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