Relevant bibliographies by topics / Aliphatic compounds

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Aliphatic compounds'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Aliphatic compounds"

1

Gordon, P. F. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 82 (1985): 109. http://dx.doi.org/10.1039/oc9858200109.

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Gordon, P. F. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 83 (1986): 99. http://dx.doi.org/10.1039/oc9868300099.

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Gordon, P. F. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 84 (1987): 113. http://dx.doi.org/10.1039/oc9878400113.

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Smith, B. V. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 85 (1988): 105. http://dx.doi.org/10.1039/oc9888500105.

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Smith, B. V. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 86 (1989): 103. http://dx.doi.org/10.1039/oc9898600103.

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Smith, B. V. "Chapter 5. Aliphatic compounds. Part (ii) Other aliphatic compounds." Annual Reports Section "B" (Organic Chemistry) 87 (1990): 117. http://dx.doi.org/10.1039/oc9908700117.

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SMITH, B. V. "ChemInform Abstract: Aliphatic Compounds. Part 2. Other Aliphatic Compounds." ChemInform 23, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.199216336.

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SMITH, B. V. "ChemInform Abstract: Aliphatic Compounds. Part 2. Other Aliphatic Compounds." ChemInform 25, no. 3 (2010): no. http://dx.doi.org/10.1002/chin.199403258.

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Yates, Peter, and J. A. Eenkhorn. "Aliphatic diazo compounds." Tetrahedron 44, no. 11 (1988): 3159–70. http://dx.doi.org/10.1016/s0040-4020(01)85947-0.

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SINGH, RS, RAHUL SINHA, and DEEPAK KUMAR SINGH. "Two new aliphatic compounds from the medicinal herb Crinum defixum." Journal of Medicinal and Aromatic Plant Sciences 35, no. 2013 (2013): 142–46. http://dx.doi.org/10.62029/jmaps.v35i3.singh.

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Two new aliphatic compounds namely 32-hydroxyheptatetracontan-21, 24-dione (A2) and oc tacosan-7, 19-di ol (A3) along with hentriacontane (A1) have been isolated from the hexane soluble extract of the shoots of the medicinal plant Crinum defixum. The structures of the compounds were elucidated on the basis of spectral and chemical studies.
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Dissertations / Theses on the topic "Aliphatic compounds"

1

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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Hoxworth, Scott. "DEGRADATION OF HALOGENATED ALIPHATIC COMPOUNDS IN SEQUENTIAL ANAEROBIC." Master's thesis, University of Central Florida, 2004. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/2803.

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The objective of this study was to utilize an alternating anaerobic/aerobic sequence to biologically transform perchloroethylene to non-hazardous end products such as ethylene, CO2 and H2 using a single microbial consortia in a methanogenic and/or a homoacetogenic environment followed by a aerobic methanotrophic environment. Reductive dechlorination of PCE and TCE to cDCE and VC in an anaerobic environment is typically carried out by methanogens, sulfidogens, or homoacetogens but often (e.g. in-situ) leads to an accumulation of daughter compounds (cDCE, VC) which are more toxic than their pare
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Liu, Zhijie. "Reductive dehalogenation of chlorinated aliphatic compounds in electrolytic systems." Diss., The University of Arizona, 1999. http://hdl.handle.net/10150/283929.

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A series of chlorinated low-molecular-weight alkanes and alkenes was transformed electrolytically at metal cathodes at potentials from -0.3 to -1.4V (vs. SHE). Products included nonchlorinated hydrocarbons and less chlorinated intermediates. Product distributions are highly dependent on cathode material and applied cathode potential. Kinetics was first-order in the concentration of the halogenated targets. The specific first-order rate constants are function of cathode potential, cathode material, solution characteristics, and reactant identify. When transformation kinetics was governed by pol
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Bacela, Siyabulela Mawande. "The evaluation of autoxidation procedures for the selective oxidation of aliphatic alcohols." Thesis, Port Elizabeth Technikon, 2001. http://hdl.handle.net/10948/59.

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The homogeneously catalyzed oxidation of 1-propanol by dioxygen in glacial acetic acid using cobalt(II)acetate and sodium bromide as the catalyst system has been investigated with the view of determining the significance of various experimental variables during the oxidation. The results of this investigation show unequivocally that a number of reaction variables have a direct influence upon catalytic activity and hence the reaction products. It is quite evident that the major product of this autoxidation reaction is propionic acid with the respective esters as side-products. This is an indica
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Dyet, Julie Anne. "Laser spectroscopy and photochemistry of C-Nitroso compounds." Thesis, Heriot-Watt University, 1987. http://hdl.handle.net/10399/1023.

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Myers, Samuel. "Electrochemical Detection of Aliphatic Sulfur Compounds in Liquid Coal Extracts." TopSCHOLAR®, 1994. http://digitalcommons.wku.edu/theses/945.

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The presence of sulfur compounds in coal is a serious environmental problem that affects the coal industry. This problem is due to the fact that organic sulfur is not separated or removed during any physical cleaning process. Organic sulfur is removed only during a more costly chemical desulfurization process. The kinds of organosulfur compounds in coal are generally known, but the quantity of each type of compound and the distribution of these compounds throughout the coal matrix has not been studied extensively. The objective of this research was to investigate the more reactive and chemical
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Scherer, Michelle Marie. "Reduction of chlorinated aliphatic and nitro aromatic compounds at the Fe0-oxide-water interface /." Full text open access at:, 1998. http://content.ohsu.edu/u?/etd,201.

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Kowlessur, Parikshant. "Engineering homoaromatic substrate specificity into aliphatic-specific Geobacillus pallidus RAPc8 nitrile hydratase." Thesis, University of the Western Cape, 2007. http://etd.uwc.ac.za/index.php?module=etd&action=viewtitle&id=gen8Srv25Nme4_9829_1297833530.

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<p>Geobacillus pallidus RAPc8 is a thermophilic nitrile-degrading isolate, obtained from thermal sediment samples of a New Zealand hot spring. The G. pallidus RAPc8 NHase gene has been cloned and expressed in E. coli. The recombinant NHase exhibits nitrile-degrading activity at 50 &deg<br>C, capable of degrading branched, linear and cyclic heteroaromatic nitrile substrates. However, no activity was found on homoaromatic nitrile substrates such as benzonitrile. In the present study, high levels of activity on benzonitrile were detected with a double mutant &beta<br>F52G&beta<br>F55L. Kinetic an
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Wu, Wai Shing. "Measurements of amino acids and aliphatic amines in ambient aerosols /." View Abstract or Full-Text, 2003. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202003%20WU.

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Thesis (M. Phil.)--Hong Kong University of Science and Technology, 2003.<br>Includes bibliographical references (leaves 226-231). Also available in electronic version. Access restricted to campus users.
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Aken, Everhard van. "Aliphatic nitro compounds in stereoselective synthesis the development of a chiral catalyst /." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 1992. http://irs.ub.rug.nl/ppn/292891849.

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Books on the topic "Aliphatic compounds"

1

Brown, B. R. The organic chemistry of aliphatic nitrogen compounds. Clarendon Press, 1994.

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V, Roberts Paul, and Robert S. Kerr Environmental Research Laboratory, eds. In-situ aquifer restoration of chlorinated aliphatics by methanotrophic bacteria. U.S. Environmental Protection Agency, Robert S. Kerr Environmental Research Laboratory, Office of Research and Development, 1989.

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Jan Rudolf van der Ploeg. Biodegradation of halogenated aliphatic compounds: Genes, enzymes and adaptation. [s.n.], 1995.

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4

Lucke, H. ALIPS, aliphatic polysulfides: Monograph of an elastomer : history, economy, chemistry, technology, applications, testing/standardization/safety of aliphatic polysulfides. Hüthig & Wepf Verlag, 1994.

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Zollinger, Heinrich. Diazo chemistry. VCH, 1995.

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Zollinger, Heinrich. Diazo chemistry.: Aromatic and heteroaromatic compounds. VCH, 1994.

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7

Sandford, Scott A. The galactic distribution of aliphatic hydrocarbons in the diffuse interstellar medium. National Aeronautics and Space Administration, 1995.

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Sandford, Scott A. The galactic distribution of aliphatic hydrocarbons in the diffuse interstellar medium. National Aeronautics and Space Administration, 1995.

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9

Dieter, Behrens, and DECHEMA, eds. DECHEMA corrosion handbook: Corrosive agents and their interaction with materials. VCH Verlagsgesellschaft (for) DECHEMA, 1990.

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G, Kreysa, Eckermann R, Behrens Dieter, and DECHEMA, eds. DECHEMA corrosion handbook: Corrosive agents and theirinteraction with materials. VCH, 1991.

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Book chapters on the topic "Aliphatic compounds"

1

Kelly, D. R. "Aliphatic compounds." In The Chemistry of Natural Products. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2144-6_9.

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Agteren, Martin H., Sytze Keuning, and Dick B. Janssen. "Aliphatic compounds." In Environment & Chemistry. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-015-9062-4_2.

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Gooch, Jan W. "Aliphatic Compounds." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_415.

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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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McCafferty, E. "Corrosion Inhibition by Fluorinated Aliphatic Compounds." In SpringerBriefs in Materials. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15648-4_6.

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Kalinowski, H. O., M. Kumar, V. Gupta, and R. Gupta. "Carbon-13 NMR of Aliphatic Compounds." In Chemical Shifts and Coupling Constants for Carbon-13. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-45285-0_2.

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Fischer, Gunther. "Aliphatic and Non-Phenolic Aromatic Compounds." In Stabilizers for Photographic Silver Halide Emulsions: Progress in Chemistry and Application. Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-9108-9_5.

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Percy, Jonathan M. "Building Block Approaches to Aliphatic Organofluorine Compounds." In Organofluorine Chemistry. Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/3-540-69197-9_4.

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Lipnick, Robert L. "Aliphatic non-electrolyte organic compounds and narcosis." In Studies of Narcosis. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3096-7_8.

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Bora, Prarthana, and Monti Gogoi. "Membrane-Based Separation of Aromatics/Aliphatic Compounds." In Application of Membranes in the Petroleum Industry. CRC Press, 2024. http://dx.doi.org/10.1201/9781003441359-5.

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Conference papers on the topic "Aliphatic compounds"

1

Angeloff, Carl, Edward P. Squiller, and Kurt E. Best. "Two Component Aliphatic Polyurea Coatings for High Productivity Applications." In SSPC 2001. SSPC, 2001. https://doi.org/10.5006/s2001-00002.

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Abstract This paper describes the development of a new class of polyurea polymer system. Specifically, the use of polyaspartic ester compounds, which are secondary aliphatic diamines, in combination with aliphatic polyisocyanates to form aliphatic polyurea coatings are described in this paper. Polyaspartic ester-based polyurea topcoats are non-yellowing, exhibit good outdoor weathering and long potlife. The moderately fast reactivity, combined with the relatively low viscosity of the polyaspartic ester compounds allows for a broader range of applications in two-component coatings.
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Squiller, Edward P., Carl Angeloff, and Kurt E. Best. "Polyaspartics: An Aliphatic Coating Technology for High Productivity Applications." In SSPC 2006. SSPC, 2006. https://doi.org/10.5006/s2006-00070.

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Abstract This paper describes the development of a new class of polyurea polymer coating. Specifically, the use of polyaspartic ester compounds, which are secondary aliphatic diamines, in combination with aliphatic polyisocyanates to form aliphatic polyurea coatings are described in this paper. Polyaspartic ester-based polyurea topcoats are non-yellowing, exhibit good outdoor weathering and long potlife. The moderately fast reactivity, combined with the relatively low viscosity of the polyaspartic ester compounds allows for a broader range of applications in two-component coatings.
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Dettman, Heather D., Nana Li, Dhanuka Wickramasinghe, et al. "The Influence of Naphthenic Acid and Sulfur Compound Structure on Global Crude Corrosivity under Vacuum Distillation Conditions." In CORROSION 2012. NACE International, 2012. https://doi.org/10.5006/c2012-01326.

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Abstract At temperatures between 220 and 400°C, naphthenic acid and sulfur-containing species present in many global crudes are known to cause refinery corrosion. Naphthenic acids are organic acids often described as cycloalkane ring(s) with an attached aliphatic chain having a terminal carboxylic acid group. Elemental sulfur, mercaptan, sulfide and polysulfide species convert to hydrogen sulfide which attacks metal. However, neither total acid contents measured by total acid number (TAN) nor total sulfur contents measured by elemental analyses have been found to correlate well with corrosivit
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Dettman, Heather D., Nana Li, and Jingli Luo. "Refinery Corrosion, Organic Acid Structure, and Athabasca Bitumen." In CORROSION 2009. NACE International, 2009. https://doi.org/10.5006/c2009-09336.

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Abstract Since 1920, certain crude oils have been found to be corrosive in refineries. At temperatures between 428 and 752°F (220 and 400°C), sulfur-containing and organic acid species in crude oils are known to promote corrosion. Elemental sulfur, mercaptan, sulfide and polysulfide species convert to hydrogen sulfide which attacks carbon and low-alloy steels. Organic acids, such as naphthenic acids consisting of cycloalkane ring(s) with an attached aliphatic chain having a terminal carboxylic acid group, have been implicated. However, neither total sulfur content measured by elemental analyse
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Growcock, F. B. "Inhibition of Steel Corrosion in Hydrochloric Acid by Acetylenic Alcohols." In CORROSION 1988. NACE International, 1988. https://doi.org/10.5006/c1988-88338.

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Abstract We have elucidated the mechanisms by which some aliphatic and aromatic acetylenic alcohols inhibit corrosion of steel in hydrochloric acid. Corrosion kinetics, electrochemical measurements and product analyses of systems containing l-octyn-3-ol, 3-phenyl-2-propyn-1-ol (3-PPO) and 1-phenyl-2-propyn-1-ol (1-PPO) indicate that, in all cases, the active inhibitor is first protonated, reversibly adsorbs and then undergoes irreversible reactions to form a polymer film. The chemisorbed inhibitor provides the majority of the corrosion protection, but the polymer film offers some protection as
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Soriaga, Manuel P., G. M. Berry, C. Bhardwaj, et al. "Chemisorption of Organic Molecules on Metal Electrode Surfaces." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90300.

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Abstract The chemisorption of various organic functional groups from aqueous solutions onto smooth single-crystal and polycrystalline electrodes, and the resistance of the resulting monolayer intermediates towards electrochemical oxidation have been studied; these investigations were motivated by the need to understand, at the atomic level, metal passivation by monolayer organic coatings. The electrodes employed were Rh, Pd, Ir, Pt, and Au whose anodic dissolution is preceded by surface-oxide formation even in highly acidic media. Resistance towards anodic oxidation can thus be associated with
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Lino dos Santos, Celia Aparecida, Gutemberg de Souza Pimenta, and Zehbour Panossian. "Study of the N-Hexane Effect in Fuel-Grade Ethanol Mixtures in Terms of Stress Corrosion Cracking of Api 5L X70 Steel." In CORROSION 2018. NACE International, 2018. https://doi.org/10.5006/c2018-11311.

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Abstract Microalloyed steels are subject to stress corrosion cracking in fuel-grade ethanol according to studies carried out in this last decade. This work identifies the key agents that cause stress corrosion cracking on API 5L X70 steel in anhydrous fuel ethanol by statistical analysis of chemical analyses data of anhydrous-ethanol samples and data from stress corrosion cracking tests previously achieved. For validation of the statistical analysis, slow-strain rate tests were carried out with API 5L X70 steel in analytical-grade anhydrous ethanol contaminated with the compounds identified in
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Tordonato, David, Bobbi Jo Merten, Allen Skaja, and Alfred Beitelman. "Secrets to Success – Examining the History and Chemistry behind the Performance of Vinyl Resin Coatings." In SSPC 2016 Greencoat. SSPC, 2016. https://doi.org/10.5006/s2016-00071.

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Abstract Solution vinyl coatings were utilized by the Bureau of Reclamation in the past and are currently used by the United States Army Corps of Engineers as a coating system that can achieve a 30-50 year service life in impacted immersion service conditions. These coatings were commonly used on gates and other equipment, which required a durable coating to withstand frequent ultraviolet (UV) light exposure, immersion service, and impact resistance. Unfortunately, solution vinyl coatings contain high fractions of volatile organic compounds (VOCs) as solvents and diluents. Federal regulation 4
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Tuckner, P. F. "Fluorocarbon Elastomer Coatings Properties, Chemistry, and Applications." In CORROSION 1987. NACE International, 1987. https://doi.org/10.5006/c1987-87239.

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Abstract Fluorocarbon elastomers have been utilized over the past 25 years for molded elastomeric parts requiring flexibility and resistance to high temperatures and harsh chemical environments. They are generally considered for applications requiring 200°C continuous service, but can operate at temperatures up to 260°C for shorter periods of time. They are also used to provide resistance to various harsh chemicals at moderate temperatures (35-150°C), showing stable physical properties and minimal volume swell. These include most aliphatic and aromatic alkanes, solvents and oils, some function
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Schwartzkopf, George, Kathleen B. Gabriel, and John B. Covington. "Evaluation of aliphatic 2-diazoketones as photoactive compounds for deep-UV lithography." In Microlithography '90, 4-9 Mar, San Jose, edited by Michael P. C. Watts. SPIE, 1990. http://dx.doi.org/10.1117/12.20100.

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Reports on the topic "Aliphatic compounds"

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Chefetz, Benny, and Baoshan Xing. Sorption of hydrophobic pesticides to aliphatic components of soil organic matter. United States Department of Agriculture, 2003. http://dx.doi.org/10.32747/2003.7587241.bard.

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Sorption of hydrophobic compounds to aliphatic components of soil organic matter (SOM) is poorly understood even though these aliphatic carbons are a major fraction of SOM. The main source of aliphatic compounds in SOM is above- and below-ground plant cuticular materials (cutin, cutan and suberin). As decomposition proceeds, these aliphatic moieties tend to accumulate in soils. Therefore, if we consider that cuticular material contributes significantly to SOM, we can hypothesize that the cuticular materials play an important role in the sorption processes of hydrophobic compounds (including pe
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Tiedje, J. M. Complete Detoxification of Short Chain Chlorinated Aliphatic Compounds: Isolation of Halorespiring Organisms and Biochemical Studies of the Dehalogenating Enzyme Systems - Final Report. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/775427.

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Tiedje, J. M. Complete detoxification of short chain chlorinated aliphatic compounds: Isolation of halorespiring organisms and biochemical studies of the dehalogenating enzyme systems. 1998 annual progress report. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/13698.

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