F Trichloroethylene

F + propene F + vinyl chloride F + vinyl bromide F + dichloroethylene F + trichloroethylene F + benzene F + toluene F 4- chlorobenzene F + bromobenzene... 

Sodium Thiosulfate, 200 F Stannic Chloride. 200 F Sulfite Liquors. 150 F Sulfur Chloride, 150 F Sulfuric Acid, 30%, 200 F Sulfuric Acid, 70%, 150 F Sulfuric Acid, 80%, 125 F Tannic Acid, 200 F Tartaric Acid, 200 F TTiiophenol, 200 F Toluene, 175 F Trichloroacetic Acid, 125 F Trichloroethylene, toiling Urea, 200 F"... 

A column is to be designed to separate the feed given below into an overhead of 99.9 mol % trichloroethylene. The top of the column will operate at 10 psig. Feed temperature is 158°F. 

C04-0158. CF3 CH2 F (HFC-134a) has replaced chlorofluorocarbon compounds for use as refrigerants. HFC-134a is produced from trichloroethylene by the following reactions ... 

Gamberale F, Aimwall G, Olson BA. 1976. Exposure to trichloroethylene. III. Psychophysiological functions. Scand J Work Environ Health 2 220-224. 

K6ssler F. 1991. Trichloroethylene interactions with muscle cells. J Appl Toxicol 11 189-194. 

Muller WF, Coulston F, Korte F. 1982. Comparative metabolism of " C-trichloroethylene in chimpanzees, baboons, and rhesus monkeys. Chemosphere 11 215-218. 

Tolot F, Viallier J, Roullett A, et al. 1964. [Hepatic toxicity of trichloroethylene.] Arch Mai Prof 25 9-15. (French)... 

Maira, A.f., Yeung, KL, Lee, C.Y., Yue, P.L, and Chan, C.K. (2000) Size effects in gas-phase photo-oxidation of trichloroethylene using nanometer-sized Ti02 catalysts. Journal of Catalysis, 192 (1), 185-196. 

R. E. Miller, F. P. Guengerich, Oxidation of Trichloroethylene by Liver Microsomal Cytochrome P450 Evidence for Chloride Migration in a Transition State not Involving Trichloroethylene Oxide , Biochemistry 1982, 21, 1090 - 1097. 

H. Cai, F. P. Guengerich, Acylation of Protein Lysines by Trichloroethylene Oxide , Chem. Res. Toxicol. 2000,13, 327 - 335 H. Cai, F. P. Guengerich, Reaction of Trichloroethylene and Trichloroethylene Oxide with Cytochrome P450 Enzymes Inactivation and Sites of Modification , Chem. Res. Toxicol. 2001, 14, 451 - 458. 

Bladan, see Parathion, Tetraethyl pyrophosphate Bladan F, see Parathion Bladan (VAN), see Tetraethyl pyrophosphate Blancosolv, see Trichloroethylene... 

Barrio-Lage, G.A., Parsons, F.Z., Nassar, R.S., and Lorenzo, P.A. Biotransformation of trichloroethylene in a variety of snbsnrface materials. Environ. Toxicol. Chem., 6(8) 571-578, 1987. 

Figure 18. Correlations between the solubility of cmchonidme and the reported empirical polarity (A) and dielectric constants (B) of 48 solvents [66]. Those solvents are indicated by the numbers in the figures 1 cyclohexane 2 n-pentane 3 n-hexane 4 triethylamine 5 carbon tetrachloride 6 carbon disulfide 7 toluene 8 benzene 9 ethyl ether 10 trichloroethylene 11 1,4-dioxane 12 chlorobenzene 13 tetrahydrofuran 14 ethyl acetate 15 chloroform 16 cyclohexanone 17 dichloromethane 18 ethyl formate 19 nitrobenzene 20 acetone 21 N,N-drmethyl formamide 22 dimethyl sulfoxide 23 acetonitrile 24 propylene carbonate 25 dioxane (90 wt%)-water 26 2-butanol 27 2-propanol 28 acetone (90 wt%)-water 29 1-butanol 30 dioxane (70 wt%)-water 31 ethyl lactate 32 acetic acid 33 ethanol 34 acetone (70 wt%)-water 35 dioxane (50 wt%)-water 36 N-methylformamide 37 acetone (50 wt%)-water 38 ethanol (50 wt%)-water 39 methanol 40 ethanol (40 wt%-water) 41 formamide 42 dioxane (30 wt%)-water 43 ethanol (30 wt%)-water 44 acetone (30 wt%)-water 45 methanol (50 wt%)-water 46 ethanol (20 wt%)-water 47 ethanol (10 wt%)-water 48 water. [Reproduced by permission of the American Chemical Society from Ma, Z. Zaera, F. J. Phys. Chem. B 2005, 109, 406-414.]...

Charbonneau M, Perreault F, Greselin E, et ah Assessment of the minimal effective dose of acetone for potentiation of the hepatoxic-ity induced by trichloroethylene-carbon tetrachloride mixtures. Fundam Appl Toxicol 10 431-438, 1988... 

Trichloroethylene — Fire Hazards Flash Point (deg. F) 90 CC practically nonflammable ... 

It is reported that trichloroethylene does not hydrolyze and is stable if temperatures in the recovery system are held below about 265° F., and that under the proper conditions of distillation, there is no danger of corrosion. The solvent, however, may decompose on excessive heating or exposure to light if antioxidants are not used (IS). 

Amra, C.H., Maronpot, R.R., Pereira, M.A., Foley, J.F., Malarkey, D.E. Anderson, M.W. (1994) ras Proto-oncogene activation in dichloroacclic acid-, trichloroethylene- and tetrachloro-ethylene-induced liver tumors inB6C3Fl mice. Carcinogenesis, 15, 2255-2261... 

Krumme, M. L., Timmis, K. N. Dwyer, D. F. (1993). Degradation of trichloroethylene by Pseudomonas cepacia G4 and the constitutive mutant strain G4 5223 PR1 in aquifer microcosms. Applied and Environmental Microbiology, 59, 2746-9. 

Ornstein, R. L. (1991)- Why timely bioremediation of synthetics may require rational enzyme redesign preliminary report on redesigning cytochrome P450cam for trichloroethylene dehalogenation. In On-Site Bioreclamation. Processes for Kenobiotic and Hydrocarbon Treatment, ed. R. E. Hinchee and R. F. Olfenbuttel, pp. 509-14. Boston Butterworth-Heinemann. 

Francesconi, R., and F. Comelli, Heat of Mixing of l,3-Dioxolane+Trichloroethylene. 

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