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TRICHLOROETHYLENE.60 Vol

CHLOROCARBONSANDCHLOROHYDROCARBONS - TRICHLOROETHYLENE] (Vol 6) -analysis by optical spectroscopy [SPECTROSCOPY, OPTICAL] (Vol 22)... [Pg.378]

Maltoni C, Lefemine G, Cotti G. 1986. Experimental research on trichloroethylene carcinogenesis. In Maltoni C, Mehlman MA, eds. Archives of research on industrial carcinogenesis series. Vol. V. Princeton, NJ Princeton Scientific Publishing Co., Inc., 393. [Pg.277]

McNeill WC Jr. 1979. Trichloroethylene. In Grayson M, Eckroth P, eds. Kirk-Othmer encyclopedia of chemical technology. 3rded. Vol. 5. New York, NY John Wiley and Sons, Inc., 745-753. [Pg.278]

Hewitt, A. D., 1999, Measurement for Trichloroethylene Relationship between Soil Vapor and Soil Matrix Environmental Testing and Analysis, May/June, Vol. 8, No. 3, pp. 25-31. [Pg.325]

Moisture Determination in Propellants and Explosives by Distillation Method 102.1.3, Pre-ecrjked by. MIL-STD-286B (1 Dec 1967). Although this procedure is similar to the one described under Dynamite in Vol 5, p D1620-ljL, we are describing it because it uses trichloroethylene (in lieu of carbon tetrachloride) as a suivciK anu a awg lu ucu ui jug/ sample ... [Pg.44]

Although these materials do not have flash points using standard ASTM test procedures, it is possible that they have flammable limits in air. For example, L-12862 has no flash point, but it does become flanunable in air between concentrations of 2.7 and 11.5 vol %. Several common materials exhibit this type of behavior. 1,1,2 Trichloroethylene does not have a flash point and is shipped as a nonflanunable material, but shows flammability limits between 12.5... [Pg.116]

Vella, P.A. and B. Veronda 1993. Oxidation of trichloroethylene A comparison of potassium permanganate and Fenton s reagent. 3nd International Symposium, Chemical Oxidation Technol-ogy for the Nineties, Nashville, TN, Technomic, Vol. 3, pp. 62-78. [Pg.433]

For dilute mixtures where the majority component is not being absorbed or stripped, the mixture components usually can be considered to behave as individual entities subject to their individual solubilities. Thus, for a mixture of 1000 ppm-vol trichloroethylene and 500 ppm-vol perchloroet-hylene, the solubility for each can be determined as if the other is absent. In general, for several components of varying solubility, the relative solubility is... [Pg.1078]

R. E. Doherty, A History of the Production and Use of Carbon Tetrachloride, Tetrachloroethylene, Trichloroethylene and i,i,i-Trichloroethane in the United States Part i—Historical Background Carbon Tetrachloride and Tetrachloroethylene, Environmental Forensics, vol. i, pp. 69-81 (2000) R. E. Doherty, A History of the Production and Use of Carbon Tetrachloride, Tetrachloroethylene, Trichloroethylene and 1,1,1 -Trichloroethane in the United States Part 2—Trichloroethylene and 1,1,1-Trichloroethane, Environmental Forensics, vol. 1, pp. 83—93 (2000) R. D. Morrison and B. L. Murphy, Chlorinated Solvents Chemistry, History and Utilization for Source Identification and Age Dating, in B. L. Murphy and R. D. Morrison, eds., Introduction to Environmental Forensics (Academic Press, San Diego, 2002), pp. 261—310. Chloromethane See chapter 4 above. [Pg.204]

CHLOROMETHYL OXIRANE (106-89-8) C3H5CIO Highly flammable, polymerizable liquid. Forms explosive mixture with air [explosion limits in air (vol %) 3.8 to 21.0 flash point 69°F/21°C 88°F/31 °C autoignition temp 772 F/411 °C Fire Rating 3]. Reacts violently with water. Contact with elevated temperatures, contamination, strong acids, strong bases, metallic halides, aluminum, aluminum chloride iron(III) chloride and other chlorides of iron or zinc can cause explosive polymerization. Violent reaction with aniline, hypochlorite, isopropylamine, potassium ieri-butoxide (ignition), sulfuric acid. Mixtures with trichloroethylene forms explosive dichloroacetylene. Incompatible with aliphatic amines, alkaline earths, alkali... [Pg.249]


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