Chlorine carbon compound with

Its specific gravity at 15° may vary from 0 855 t0 0 88o, but usually lies between o 86o and o 875 the specific gravity increases with lapse of time owing to Testification The presence of mineral oils lowers the density, whilst that of tar oils or chlorinated carbon compounds raises it. 

In this lecture some new routes to phosphorus-carbon compounds with P-C multiple bonds, found in connection with our investigations on reactions of tertiary phosphanes with chlorinated carbon compounds, such as tetrachloromethane, hexachloroethane, phosgene, and isocyanide dichlorides are reported. Furthermore some stereochemical problems concerning this type of compound will be discussed. 

Indeed, the combination of a lack of water and the presence of halogens or halides is the major reason for zirconium to experience corrosion problems in organic solutions. For example, addition of some water can suppress zirconium s susceptibility to SCC in alcohol solutions with halide impurities. Qn the other hand, zirconium shows excellent corrosion resistance in certain chlorinated carbon compounds, e.g., carbon... 

Carbon monoxide forms addition compounds. With chlorine in sunlight or in the presence of charcoal in the dark, carbonyl chloride... 

Manufacture. Trichloromethanesulfenyl chloride is made commercially by chlorination of carbon disulfide with the careful exclusion of iron or other metals, which cataly2e the chlorinolysis of the C—S bond to produce carbon tetrachloride. Various catalysts, notably iodine and activated carbon, are effective. The product is purified by fractional distillation to a minimum purity of 95%. Continuous processes have been described wherein carbon disulfide chlorination takes place on a granular charcoal column (59,60). A series of patents describes means for yield improvement by chlorination in the presence of dihinctional carbonyl compounds, phosphonates, phosphonites, phosphites, phosphates, or lead acetate (61). 

The 50.31 MHz 13C NMR spectra of the chlorinated alkanes were recorded on a Varian XL-200 NMR spectrometer. The temperature for all measurements was 50 ° C. It was necessary to record 10 scans at each sampling point as the reduction proceeded. A delay of 30 s was employed between each scan. In order to verify the quantitative nature of the NMR data, carbon-13 Tj data were recorded for all materials using the standard 1800 - r -90 ° inversion-recovery sequence. Relaxation data were obtained on (n-Bu)3SnH, (n-Bu)3SnCl, DCP, TCH, pentane, and heptane under the same solvent and temperature conditions used in the reduction experiments. In addition, relaxation measurements were carried out on partially reduced (70%) samples of DCP and TCH in order to obtain T data on 2-chloropentane, 2,4-dichloroheptane, 2,6-dichloroheptane, 4-chloroheptane, and 2-chloroheptane. The results of these measurements are presented in Table II. In the NMR analysis of the chloroalkane reductions, we measured the intensity of carbon nuclei with T values such that a delay time of 30 s represents at least 3 Tj. The only exception to this is heptane where the shortest T[ is 12.3 s (delay = 2.5 ). However, the error generated would be less than 10%, and, in addition, heptane concentration can also be obtained by product difference measurements in the TCH reduction. Measurements of the nuclear Overhauser enhancement (NOE) for carbon nuclei in the model compounds indicate uniform and full enhancements for those nuclei used in the quantitative measurements. Table II also contains the chemical... 

Kirkpatrick, M.J., Finney, W.C. and Locke, B.R. (2003) Chlorinated organic compound removal by gas phase pulsed streamer corona electrical discharge with reticulated vitreous carbon electrodes, Plasmas and Polymers 8, 165-77. 

BMS A process for removing mercury from the effluent from the Castner-Kellner process. Chlorine is used to oxidize metallic mercury to the mercuric ion, and this is then adsorbed on activated carbon impregnated with proprietary sulfur compounds. Developed by Billingsfors Bruks, Sweden. 

Pyral A process for destroying toxic waste oiganochlorine compounds. The wastes are mixed with carbon and sodium carbonate and injected into a graphite-lined arc furnace. Metallic sodium, formed by reduction of the sodium carbonate by the carbon, attacks the chlorinated organic compounds, forming sodium chloride. Developed by Hydro-Quebec in the late 1980s but not yet commercialized. 

Hexachloroethane does not occur naturally in the environment. It is made by adding chlorine to tetrachloroethylene. Hexachloroethane is no longer made in the United States, but it is formed as a byproduct in the production of some chemicals. For example, it is a by-product in the high temperature synthesis of tetrachloroethylene from carbon tetrachloride. Some hexachloroethane can be formed by incinerators when materials containing chlorinated hydrocarbons are burned. Hexachloroethane itself does not easily catch fire. Some hexachloroethane can also be formed when chlorine reacts with carbon compounds in drinking water. 

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