Academic literature on the topic 'Halogenated compound'

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Journal articles on the topic "Halogenated compound"

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Gao, Peng, and Ying Huang. "Detection, Distribution, and Organohalogen Compound Discovery Implications of the Reduced Flavin Adenine Dinucleotide-Dependent Halogenase Gene in Major Filamentous Actinomycete Taxonomic Groups." Applied and Environmental Microbiology 75, no. 14 (2009): 4813–20. http://dx.doi.org/10.1128/aem.02958-08.

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ABSTRACT Halogenases have been shown to play a significant role in biosynthesis and introducing the bioactivity of many halogenated secondary metabolites. In this study, 54 reduced flavin adenine dinucleotide (FADH2)-dependent halogenase gene-positive strains were identified after the PCR screening of a large collection of 228 reference strains encompassing all major families and genera of filamentous actinomycetes. The wide distribution of this gene was observed to extend to some rare lineages with higher occurrences and large sequence diversity. Subsequent phylogenetic analyses revealed that
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Zakary, sefatullah, Habeebat Oyewusi, and Fahrul Huyop. "Dehalogenases for pollutant degradation in brief: A mini review." Journal of Tropical Life Science 11, no. 1 (2021): 17–24. http://dx.doi.org/10.11594/jtls.11.01.03.

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Dehalogenases are microbial enzyme catalysed the cleavage of carbon-halogen bond of halogenated organic compounds. It has potential use in the area of biotechnology such as bioremediation and chemical industry. Halogenated organic compounds can be found in a considerable amount in the environment due to utilization in agriculture and industry, such as pesticides and herbicides. The presence of halogenated compound in the environment have been implicated on the health and natural ecosystem. Microbial dehalogenation is a significant method to tackle this problem. This review intends to briefly d
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Gedye, Richard Neville, Yoginder Nath Sadana, and Raymond Leger. "The electroreduction of halogenated thiophenes." Canadian Journal of Chemistry 63, no. 10 (1985): 2669–72. http://dx.doi.org/10.1139/v85-443.

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Electroreduction of polyhalothiophenes results in the preferential reduction of the α-halogen atoms. Preparative electrochemical reduction of these compounds at controlled potential can be used to synthesize 2,3,4-trihalo, 3,4-dihalo, and 3-halothiophenes. Experimental conditions were developed under which these reductions could be done selectively, giving good yields of the desired products. Electroreduction of tetrabromothiophene can also lead to the formation of a poly-bromodithienyl mercury compound.
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Sithole, Bishop B., and David T. Williams. "Halogenated Phenols in Water at Forty Canadian Potable Water Treatment Facilities." Journal of AOAC INTERNATIONAL 69, no. 5 (1986): 807–10. http://dx.doi.org/10.1093/jaoac/69.5.807.

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Abstract Samples of raw and treated water were collected once in each of 3 seasons at 40 potable water treatment plants across Canada and were analyzed for phenol and 33 halogenated phenolic compounds including chlorophenols, bromophenols, bromochlorophenols, and chloroguaiacols. Eighteen of the compounds were not found at any treatment plant; phenol and each of the remaining halogenated phenols were found in at least 1 sample. Pentachlorophenol was the only halogenated phenolic compound found in more than 20% of the raw water samples in the fall and winter samples at levels up to 53 ng/L with
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Ninga, Ederina, Elvira Beli, Elona Shahu, and Ilirjana Boci. "Analysis of Halogenated Compounds in Fish Samples." European Journal of Engineering Research and Science 4, no. 2 (2019): 37–39. http://dx.doi.org/10.24018/ejers.2019.4.2.1099.

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The paper reports investigation on the presence of 13 halogenated compounds (six chlorinated compounds, nd-like PCBs and seven brominated compounds, polybrominated diphenyl ethers (PBDEs)), in five marine species which are part on Albanian consumer diet. The samples were extracted with ethyl acetate and treated with sulfuric acid. Extract was analyzed simultaneously using gas chromatography tandem mass spectrometry. Presence of PCBs was confirmed at1.4 percent of the samples. The most dominated congener found to be present were PCB 153 and PCB 138. Form the brominated compounds 2,2′,4,4′-tetra
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Moqadam, Samira, and Mehdi Salami-Kalajahi. "Halogenated sunflower oil as a precursor for synthesis of polysulfide polymer." e-Polymers 16, no. 1 (2016): 33–39. http://dx.doi.org/10.1515/epoly-2015-0152.

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AbstractPolysulfide polymers usually are prepared by the reaction of different dihalide compounds with disodium polysulfides. In this field, dihalides are expensive and produced from halogenation of organic compounds by different methods with harsh conditions. To overcome this problem, in this work, sunflower oil as polyunsaturated oil was used as precursor to produce polyhalide compound. In this field, double bonds of oil were applied as functional groups to halogenate the sunflower via benzoyl peroxide-catalyzed reaction with hydrochloric acid. Also, Na2S3 was synthesized via the reaction be
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Shiyanga, Aina N., Michael Knott, and Petrina Kapewangolo. "In vitro Anti-HIV and Antimicrobial Activities of a Halogenated Monoterpene from a Namibian Plocamium Species of Marine Algae." Current Bioactive Compounds 16, no. 3 (2020): 363–67. http://dx.doi.org/10.2174/1573407215666190111153845.

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Background: The marine red alga Plocamium naturally produces halogenated monoterpenes with varied biological activities. In our continuing efforts to discover new lead compounds for the treatment of HIV/AIDS as well as novel antibacterial compounds, various Namibian Plocamium species have been investigated. Methods: A rare but known compound namely 1E,3R,4S,5E,7Z-1-bromo-3,4,8-trichloro-7- (dichloromethyl)-3-methylocta-1,5,7-triene (1) was isolated from a Namibian Plocamium red alga. The anti-HIV activity of compound 1 was investigated against three HIV enzymes namely, HIV protease, reverse tr
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Tanase, Constantin I., Lucia Pintilie та Elena Mihai. "A Molecular Docking of New 9β-Halogenated Prostaglandin Analogs with an Ester Group at C-6 Atom of the α-Side Chain". Revista de Chimie 71, № 4 (2020): 101–10. http://dx.doi.org/10.37358/rc.20.4.8048.

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Prostaglandins with cytoprotective activity were studied for a long time and a few PGE1 and PGE2 stable analogs were promoted as drugs: arbaprostil, enprostil, misoprostol and rioptostol. Nocloprost, a 9β-chlorine prostaglandin analog, has been also promoted as a cytoprotective drug; the succes with this compound stimulated the reserches, and many 9β- or 11β-substituted prostaglandins were synthesized and studied for their biological activity. In the same dirrection we previously synthesized new 9β-halogenated prostaglandins having also an ester group at the carbon atom 6. These compounds were
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den Besten, C., A. Brouwer, I. M. C. M. Rietjens, and P. J. van Bladeren. "Biotransfiormation and Toxicity of Halogenated Benzenes." Human & Experimental Toxicology 13, no. 12 (1994): 866–75. http://dx.doi.org/10.1177/096032719401301209.

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1 Multiple potentially harmful metabolites can be distinguished in the metabolic activation of halogenated benzenes: epoxides, phenols, benzoquinones and benzoquinone-derived glutathione conjugates. 2 The role of these (re-) active metabolites in the toxic effects induced by halogenated benzenes such as hepatotoxicity, nephrotoxicity, porphyria and thyroid toxicity is discussed. 3 Evidence is presented suggesting that the formation of reactive benzoquinone metabolites rather than the traditional epoxides is linked to halogenated benzene-induced hepatotoxicity. 4 A crucial role for the benzoqui
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Wang, Guangli, Rong Li, Shunpeng Li, and Jiandong Jiang. "A Novel Hydrolytic Dehalogenase for the Chlorinated Aromatic Compound Chlorothalonil." Journal of Bacteriology 192, no. 11 (2010): 2737–45. http://dx.doi.org/10.1128/jb.01547-09.

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ABSTRACT Dehalogenases play key roles in the detoxification of halogenated aromatics. Interestingly, only one hydrolytic dehalogenase for halogenated aromatics, 4-chlorobenzoyl-coenzyme A (CoA) dehalogenase, has been reported. Here, we characterize another novel hydrolytic dehalogenase for a halogenated aromatic compound from the 2,4,5,6-tetrachloroisophthalonitrile (chlorothalonil)-degrading strain of Pseudomonas sp. CTN-3, which we have named Chd. Chd catalyzes a hydroxyl substitution at the 4-chlorine atom of chlorothalonil. The metabolite of the Chd dehalogenation, 4-hydroxy-trichloroisoph
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Dissertations / Theses on the topic "Halogenated compound"

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Rehfuss, Marc Y. "Characterization and phylogenetic analysis of a phenol and halogenated aromatic compound degrading microbial consortium /." Search for this dissertation online, 2004. http://wwwlib.umi.com/cr/ksu/main.

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Smith, Madelyn M. "Cometabolic Degradation of Halogenated Aliphatic Hydrocarbons by Aerobic Microorganisms Naturally Associated with Wetland Plant Roots." Wright State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=wright1341854406.

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Nijenhuis, Ivonne [Verfasser], R. Gary [Akademischer Betreuer] Sawers, G. [Akademischer Betreuer] Diekert, and Lollar B. [Akademischer Betreuer] Sherwood. "Characterisation of microbial transformation of halogenated organic contaminants using compound-specific stable isotope analysis / Ivonne Nijenhuis. Betreuer: R. Gary Sawers ; G. Diekert ; B. Sherwood Lollar." Halle, Saale : Universitäts- und Landesbibliothek Sachsen-Anhalt, 2016. http://d-nb.info/109078662X/34.

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Paschoalato, Cristina Filomêna Pereira Rosa. "Efeito da pré-oxidação, coagulação, filtração e pós-cloração na formação de subprodutos orgânicos halogenados em águas contendo substâncias húmicas." Universidade de São Paulo, 2005. http://www.teses.usp.br/teses/disponiveis/18/18138/tde-04022016-122828/.

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A presença de substâncias húmicas em águas destinadas ao abastecimento tem ocasionado diversos problemas, decorrentes da formação de subprodutos orgânicos halogenados, principalmente quando se emprega a pré-oxidação com cloro. Os compostos orgânicos halogenados, reconhecidamente carcinogênicos e que podem ser encontrados nas águas tratadas e distribuída à população, são: trialometanos, ácidos haloacéticos, haloaldeidos, halocetonas, halofenóis e halopicrinas. Nas estações de tratamento de água para abastecimento (ETAs), a utilização da etapa de pré-oxidação da água bruta com cloro contribui pa
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Connell, Richenda K. "Tropospheric degradation of halogenated compounds." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320615.

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Huang, Jinqing, and 黃普卿. "A study of the reaction mechanisms and reactive intermediates involved in halogenated compounds : trichloroethylene oxide, halogenated benzophenones, and halogenated quinoline-based phototriggers." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2014. http://hdl.handle.net/10722/208036.

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UV/Vis absorption spectroscopy (UV/Vis), femtosecond transient absorption spectroscopy (fs-TA), nanosecond transient absorption spectroscopy (ns-TA), and nanosecond time-resolved resonance Raman spectroscopy (ns-TR3), as well as density functional theory (DFT) computations were employed to study the mechanisms and the intermediates in reactions of selected halogenated compounds, including trichloroethylene oxide (TCE oxide), halogenated benzophenones (4-FBP, 4-ClBP, 4-BrBP, 3-FBP, 33’-DFBP, 3-ClBP, 3-BrBP, 2-FBP, 2-ClBP, and 2-BrBP), and halogenated quinoline-based phototriggers (BHQ-OPh and B
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Greenacre, Caroline M. "Tropospheric chemistry of halogenated organic compounds." Thesis, University of Oxford, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.404120.

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Kinnison, David J. A. "Tropospheric chemistry of halogenated organic compounds." Thesis, University of Oxford, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.240663.

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Armfield, Susan J. "Microbial dehalogenation of halogenated aliphatic compounds." Thesis, University of Kent, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253744.

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Allpress, James David. "Microbial transformation of halogenated organic compounds." Thesis, Manchester Metropolitan University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.309883.

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Books on the topic "Halogenated compound"

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Kirk, Kenneth L. Biochemistry of Halogenated Organic Compounds. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4757-4605-1.

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Biochemistry of halogenated organic compounds. Plenum Press, 1991.

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IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Chlorinated drinking-water, chlorination by-products: Some other halogenated compounds, cobalt and cobalt compounds. International Agency for Research on Cancer, 1991.

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Al-Haddad, Ameera S. Chromatographic and spectroscopic studies of halogenated aromatic compounds. University of East Anglia, 1989.

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service), SpringerLink (Online, ed. Halogenated Heterocycles: Synthesis, Application and Environment. Springer Berlin Heidelberg, 2012.

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Peverall, Robert. Negative ion and electron attachment reactions with a variety of halogenated compounds. University of Birmingham, 1995.

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International Symposium on Halogenated Environmental Organic Pollutants and POPs (19th 1999 Venice, Italy). Dioxin 99: 19th International Symposium on Halogenated Environmental Organic Pollutants and POPs : September 12-17, 1999, Venice, Italy : [short papers]. International Symposium on Halogenated Environmental Organic Pollutants and POPs, 1999.

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International Symposium on Halogenated Environmental Organic Pollutants and POPs (23rd 2003 Boston, Mass.). Dioxin 2003: 23rd International Symposium on Halogenated Environmental Organic Pollutants and Persistent Organic Pollutants (POPs) : Boston, Massachusetts, USA, August 24-29, 2003. International Symposium on Halogenated Environmental Organic Pollutants and Persistent Organic Pollutants (POPs), 2003.

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Dioxin, 2001 (2001 Kyŏngju-si Korea). Dioxin 2001: 21st International Symposium on Halogenated Environmental Organic Pollutants and Persistent Organic Pollutants (POPs), held 9-14 September 2001, Gyeongju, Korea. Dr. Jae-Ho Yang, Catholic University of Daegu, 2001.

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International Symposium on Halogenated Environmental Organic Pollutants and POPs (20th 2000 Monterey, Calif.). Dioxin 2000: 20th International symposium on halogenated environmental organic pollutants and persistent organic pollutants (POPs), Monterey, California, USA. August 13-17, 2000. Edited by Denison Michael S and United States. Environmental Protection Agency. University of California, 2000.

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Book chapters on the topic "Halogenated compound"

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Agteren, Martin H., Sytze Keuning, and Dick B. Janssen. "Halogenated aliphatic compounds." In Environment & Chemistry. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-015-9062-4_3.

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O'Doherty, Simon J., and Lucy J. Carpenter. "Halogenated Volatile Organic Compounds." In Volatile Organic Compounds in the Atmosphere. Blackwell Publishing Ltd, 2007. http://dx.doi.org/10.1002/9780470988657.ch5.

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Commandeur, L. C. M., and J. R. Parsons. "Degradation of halogenated aromatic compounds." In Physiology of Biodegradative Microorganisms. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3452-1_10.

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Majer, J. R., and J. P. Simons. "Photochemical Processes in Halogenated Compounds." In Advances in Photochemistry. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470133323.ch4.

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Rondinini, Sandra, and Alberto Vertova. "Electroreduction of Halogenated Organic Compounds." In Electrochemistry for the Environment. Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-68318-8_12.

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Commandeur, Laetitia C. M., and John R. Parsons. "Biodegradation of halogenated aromatic compounds." In Biochemistry of microbial degradation. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1687-9_13.

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Kirk, Kenneth L. "Metabolism of Halogenated Compounds—Biodehalogenation." In Biochemistry of the Elemental Halogens and Inorganic Halides. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-5817-6_9.

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Kirk, Kenneth L. "Biochemistry of Halogenated Carbohydrates." In Biochemistry of Halogenated Organic Compounds. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4757-4605-1_6.

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Kirk, Kenneth L. "Biochemistry of Halogenated Carboxylic Acids." In Biochemistry of Halogenated Organic Compounds. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4757-4605-1_1.

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Kirk, Kenneth L. "Biochemistry of Halogenated Amino Acids." In Biochemistry of Halogenated Organic Compounds. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4757-4605-1_7.

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Conference papers on the topic "Halogenated compound"

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Takahira, Kazuya, Asuki Toda, Katsumi Suzuki, Takeshi Fukuda, Norihiko Kamata, and Zentaro Honda. "Organic photovoltaic cell fabricated by electrospray deposition using non-halogenated solvent." In 2016 Compound Semiconductor Week (CSW) [Includes 28th International Conference on Indium Phosphide & Related Materials (IPRM) & 43rd International Symposium on Compound Semiconductors (ISCS)]. IEEE, 2016. http://dx.doi.org/10.1109/iciprm.2016.7528712.

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Sadiek, Ibrahim, Adrian Hjältén, Michael Stuhr, Chuang Lu, Francisco Senna Vieira, and Aleksandra Foltynowicz. "Mid-Infrared Comb-Based Fourier Transform Spectroscopy of Halogenated Volatile Organic Compounds." In CLEO: Science and Innovations. OSA, 2020. http://dx.doi.org/10.1364/cleo_si.2020.sm1m.8.

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Li, Jianrong, Stefan Persijn, Iris de Krom, Heleen Meuzelaar, and Adriaan M. H. van der Veen. "Metrology for biomethane conformity assessment: measure trace gas impurities in biomethane." In 19th International Congress of Metrology (CIM2019), edited by Sandrine Gazal. EDP Sciences, 2019. http://dx.doi.org/10.1051/metrology/201906002.

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To facilitate the use of biomethane in existing transmission and distribution infrastructures, CEN/TC 408 developed specifications (EN 16723) for injecting biomethane into the natural gas grids and using it as a transport fuel. Currently, the test methods cited in EN 16723 lack metrological aspects and have not been specifically developed for biomethane. To address this need, ISO/TC193/SC1/WG25 “Biomethane” has been created to work on standardized methods. To assess conformity of biomethane with the specification and to provide essential input to WG25, test methods are being developed in this
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Soares, Evellyn E., Vytor P. Oliveira, and Bruna L. Marcial. "Theoretical pKa prediction of halogenated compounds in aqueous solution using an implicit solvation model." In VII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Editora Letra1, 2018. http://dx.doi.org/10.21826/9788563800374018.

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Ghanadzadeh, A., A. Ranjkesh, H. Ghanadzadeh, and M. M. Moghadam. "Dielectric study and molecular interaction of halogenated compounds in non-polar solvent at different temperatures." In 2008 IEEE International Conference on Dielectric Liquids (ICDL 2008). IEEE, 2008. http://dx.doi.org/10.1109/icdl.2008.4622501.

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Kosmas, Agnie M., Antonija Lesar, Theodore E. Simos, and George Maroulis. "Halogenated Methyl Nitrates, CX[sub 3]ONO[sub 2] (X = F, Cl). A Computational Study of their Properties and Capacity to Act as Sink Compounds in the Troposphere." In COMPUTATIONAL METHODS IN SCIENCE AND ENGINEERING: Theory and Computation: Old Problems and New Challenges. Lectures Presented at the International Conference on Computational Methods in Science and Engineering 2007 (ICCMSE 2007): VOLUME 1. AIP, 2007. http://dx.doi.org/10.1063/1.2836204.

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Reports on the topic "Halogenated compound"

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John F. Schabron, Jr Joseph F. Rovani, and Theresa M. Bomstad. FIELD SCREENING FOR HALOGENATED VOLATILE ORGANIC COMPOUNDS. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/820761.

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John F. Schabron, Joseph F. Rovani Jr., and Theresa M. Bomstad. FIELD SCREENING FOR HALOGENATED VOLATILE ORGANIC COMPOUNDS. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/822157.

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John F. Schabron, Susan S. Sorini, and Joseph F. Rovani Jr. FIELD SCREENING FOR HALOGENATED VOLATILE ORGANIC COMPOUNDS: THE NEW X-WAND HVOC SCREENING DEVICE. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/887237.

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Lunsford, J. H. The Adsorption and Reactions of Halogenated Volatile Organic Compounds (VOCs) on Metal Oxides - Final Report. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/775042.

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Lunsford, J., D. W. Goodman, and J. F. Haw. The adsorption and reaction of halogenated volatile organic compounds (VOC's) on metal oxides. 1998 annual progress report. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/13641.

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Lunsford, J. H., J. F. Haw, and D. W. Goodman. The adsorption and reaction of halogenated volatile organic compounds (VOC's) on metal oxides. Annual progress report, September 1996--October 1997. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/13640.

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