Relevant bibliographies by topics / Chlorobutane

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Chlorobutane'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Chlorobutane"

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Domínguez, M., A. Camacho, M. C. López, F. M. Royo, and J. S. Urieta. "Excess molar volumes and excess viscosities of ternary mixtures (2-butanol + 1-chlorobutane + 1-butylamine) and (2-methyl-2-propanol + 1-chlorobutane + 1-butylamine) at 298. 15 K." Canadian Journal of Chemistry 73, no. 6 (1995): 896–901. http://dx.doi.org/10.1139/v95-112.

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Excess molar volumes and excess viscosities, at 298.15 K, of the ternary mixtures (2-butanol + 1-chlorobutane + 1-butylamine) and (2-methyl-2-propanol + 1-chlorobutane + 1-butylamine) and of the binary mixtures (2-butanol + 1-butylamine), (2-methyl-2-propanol + 1-butylamine), and (1-chlorobutane + 1-butylamine) have been measured. The ternary excess properties were fitted to the polynomial equation of Cibulka. The experimental results were also compared with those predicted by the empirical equations of Redlich–Kister, Tsao–Smith, Kohler, and Colinet. Keywords: binary and ternary mixtures, exc
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Vanderberg, Laura A., and Jerome J. Perry. "Dehalogenation by Mycobacterium vaccae JOB-5: role of the propane monooxygenase." Canadian Journal of Microbiology 40, no. 3 (1994): 169–72. http://dx.doi.org/10.1139/m94-029.

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Mycobacterium vaccae JOB-5 has an inducible propane monooxygenase that has been implicated in the catabolism of most major groundwater pollutants including trichloroethylene. Propane-grown cells are also induced for the dehalogenation of 1-chlorobutane and other chloroalkanes. 1-Chlorobutane is oxidized to 2-butanol, indicating that subterminal oxidation of 1-chlorobutane resulted in a concomitant release of the chloride. Nonproliferating suspensions of M. vaccae induced for the propane monooxygenase can dehalogenate a variety of chlorinated hydrocarbons including monochlorinated alcohols, dic
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Chang, Yu-Hsu, and Hsin-Tien Chiu. "Nano-sizing titanium into titanium carbide by 1-chlorobutane." Journal of Materials Research 17, no. 11 (2002): 2779–82. http://dx.doi.org/10.1557/jmr.2002.0403.

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TiC nanoparticles (average diameter 10–150 nm) were prepared by reacting bulk Ti powders (average diameter 20 μm) with gaseous 1-chlorobutane at a relatively low temperature (1073–1273 K). 1-Chlorobutane provided the carbon atom in the TiC and the chlorine atom that assisted the shrinking of the size of the original Ti powders. The apparently simple procedure is a complex heterogeneous process combining etching, deposition, and carburization reactions.
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Wisniak, J. "Vapor-Liquid Equilibria in the Ternary System 2-Chlorobutane + 1-Chlorobutane + Cyclohexane and Its Binaries." Physics and Chemistry of Liquids 29, no. 4 (1995): 243–55. http://dx.doi.org/10.1080/00319109508031642.

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Wisniak, Jaime, Alexander Apelblat, Jacob Zabicky, and Ina Feingold. "Isobaric Vapor—Liquid Equilibria in the Binary Systems of 1,3-Dioxolane, 1-Chlorobutane and 2-Chlorobutane." Physics and Chemistry of Liquids 28, no. 3 (1994): 177–85. http://dx.doi.org/10.1080/00319109408034666.

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Wang, Junjie, Xiaowen Tang, Yanwei Li, et al. "Computational evidence for the degradation mechanism of haloalkane dehalogenase LinB and mutants of Leu248 to 1-chlorobutane." Physical Chemistry Chemical Physics 20, no. 31 (2018): 20540–47. http://dx.doi.org/10.1039/c8cp03561j.

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Wisniak, Jaime. "Vapor-Liquid Equilibria in the Systems 2,2'-Oxybis[propane] + 1-Chlorobutane and 2,2'-Oxybis[propane] + 1-Chlorobutane + Cyclohexane." Journal of Chemical & Engineering Data 40, no. 5 (1995): 1140–44. http://dx.doi.org/10.1021/je00021a025.

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Demir, Ayhan S., and Dieter Enders. "Synthesis of Bicyclic and Tricyclic Enones via Regioselective Dialkylation of Cyclic 1,3-Diketone-dimethylhydrazones with 4-Chlorobutane-2-one." Zeitschrift für Naturforschung B 44, no. 7 (1989): 834–38. http://dx.doi.org/10.1515/znb-1989-0718.

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An efficient, regioselective synthesis of substituted bicyclo nonenes and decenes of type (4a, b) and the tricyclic tetradecadiene (5) is described. The key step is the regioselective dialkylation of cyclic 1,3-diketone-dimethylhydrazones (la—e) with 4-chlorobutane-2-one.
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Poelarends, Gerrit J., Leonid A. Kulakov, Michael J. Larkin, Johan E. T. van Hylckama Vlieg, and Dick B. Janssen. "Roles of Horizontal Gene Transfer and Gene Integration in Evolution of 1,3-Dichloropropene- and 1,2-Dibromoethane-Degradative Pathways." Journal of Bacteriology 182, no. 8 (2000): 2191–99. http://dx.doi.org/10.1128/jb.182.8.2191-2199.2000.

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ABSTRACT The haloalkane-degrading bacteria Rhodococcus rhodochrous NCIMB13064, Pseudomonas pavonaceae 170, and Mycobacterium sp. strain GP1 share a highly conserved haloalkane dehalogenase gene (dhaA). Here, we describe the extent of the conserved dhaA segments in these three phylogenetically distinct bacteria and an analysis of their flanking sequences. The dhaA gene of the 1-chlorobutane-degrading strain NCIMB13064 was found to reside within a 1-chlorobutane catabolic gene cluster, which also encodes a putative invertase (invA), a regulatory protein (dhaR), an alcohol dehydrogenase (adhA), a
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Teodorescu, Mariana, and Ivan Wichterle. "Evaluation of the Carbonyl/Chlorine Interaction Parameters in Pentan-3-one-Chloroalkane Mixtures Using the Disquac Group Contribution Model." Collection of Czechoslovak Chemical Communications 65, no. 10 (2000): 1559–72. http://dx.doi.org/10.1135/cccc20001559.

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Thermodynamic behaviour of the eight systems containing pentan-3-one and a chloroalkane, namely 1-chlorobutane, 1,2-dichloroethane, 1,3-dichloropropane, 1,4-dichlorobutane, trichloromethane, 1,1,1-trichloroethane, tetrachloromethane and 1,1,2,2-tetrachloro- ethane was interpreted in terms of the DISQUAC group contribution model. It was found that quasichemical term for the contact C=O/Cl in the pentan-3-one-α,ω-dichloroalkane and pentan-3-one-1,1,1-trichloroethane systems is not negligible. The DISQUAC dispersive interchange parameters for C=O/Cl contact in these systems were evaluated from li
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Dissertations / Theses on the topic "Chlorobutane"

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Tan, Leng Leng. "Catalytic dehydrochlorination of 2-chlorobutane." Thesis, Cardiff University, 2005. http://orca.cf.ac.uk/55552/.

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The catalytic dehydrochlorination of 2-chlorobutane has been studied using promoted alumina catalysts. The modified alumina (AI2O 3-HCI, K-AI2O3), zirconia-alumina (Zr02-Al203) and silver-alumina (Ag/AC) catalysts were synthesized and characterised before being tested for catalyst activity. In addition, silver-silica (Ag/SiC) and silver-zirconia-alumina (Ag/ZrCVAhOs) were also prepared as different supported silver catalysts for dehydrochlorination of 2-chlorobutane. y-alumina catalysts were active for the dehydrochlorination reaction due to the presence of Lewis acid sites. The catalyst perfo
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Kondaveeti, Rajiv. "Impact of Halogenated Aliphatic and Aromatic Additives on Soot and Polycyclic Aromatic Hydrocarbons -- An Ethylene-air Laminar Co-flow Diffusion Flame Study." University of Dayton / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1343786258.

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歐鳳昭. "Vapor-Liquid Equilibria of Isopropanol+1-Chlorobutabe+Acetonitrile at 101.3kPa." Thesis, 1997. http://ndltd.ncl.edu.tw/handle/26892836122021431233.

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碩士<br>靜宜大學<br>應用化學研究所<br>85<br>Vapor-Liquid Equilibrium is a necessary element for desinging and developing chemical processes as well as enhancing our understanding of fluid-phase behaviors. In this work, VLE data of binary and ternary systems of Isopropanol + 1-Chlorobutane + Acetonitrile have been measured under constant pressure of 101.3 kPa. Experimental data of the binary systems of Isopropanol + 1-Chlorobutane, Isopropanol + Acetonitrile and 1- Chlorobutane + Acetonitrile were thermodynamic consistent via Herington analysis. In the treatment of experimental data, both binary sy
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Book chapters on the topic "Chlorobutane"

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Wohlfarth, Ch. "Viscosity of 1-chlorobutane." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_109.

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Wohlfarth, Ch. "Viscosity of 2-chlorobutane." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_110.

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Demaison, J. "484 C4H9Cl 1-Chlorobutane." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_232.

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Wohlfarth, Christian. "Viscosity of 1-chlorobutane." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_105.

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Wohlfarth, Christian. "Viscosity of 2-chlorobutane." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_106.

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Wohlfarth, Ch. "Refractive index of 1-chlorobutane." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38). Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_98.

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Wohlfarth, Ch. "Refractive index of 2-chlorobutane." In Refractive Indices of Pure Liquids and Binary Liquid Mixtures (Supplement to III/38). Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75291-2_99.

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Wohlfarth, Christian. "Surface tension of 1-chlorobutane." In Surface Tension of Pure Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48336-7_61.

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Wohlfarth, Christian. "Surface tension of 2-chlorobutane." In Surface Tension of Pure Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48336-7_62.

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Wohlfarth, Ch. "Surface tension of 1-chlorobutane." In Supplement to IV/16. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75508-1_71.

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Conference papers on the topic "Chlorobutane"

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Tafat-Igoudjilene, O., L. Mostefai, and A. Ait Kaci. "Experimental and Predicted Excess Molar Volumes of Ternary Mixtures (1-chlorobutane or 2-methyl, 2-chloro propane) + n-heptane + 2-pentanone at T=298,15 K." In XXXV JEEP – 35th Conference on Phase Equilibria. EDP Sciences, 2009. http://dx.doi.org/10.1051/jeep/200900024.

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