Chloride ethylene dichloride

Dichloroethane [107-06-2] ethylene chloride, ethylene dichloride, CH2CICH2CI, is a colorless, volatile Hquid with a pleasant odor, stable at ordinary temperatures. It is miscible with other chlorinated solvents and soluble in common organic solvents as well as having high solvency for fats, greases, and waxes. It is most commonly used in the production of vinyl chloride monomer. 

NOTE - Petrochemical plants also generate significant amounts of solid wastes and sludges, some of which may be considered hazardous because of the presence of toxic organics and heavy metals. Spent caustic and other hazardous wastes may be generated in significant quantities examples are distillation residues associated with units handling acetaldehyde, acetonitrile, benzyl chloride, carbon tetrachloride, cumene, phthallic anhydride, nitrobenzene, methyl ethyl pyridine, toluene diisocyanate, trichloroethane, trichloroethylene, perchloro-ethylene, aniline, chlorobenzenes, dimethyl hydrazine, ethylene dibromide, toluenediamine, epichlorohydrin, ethyl chloride, ethylene dichloride, and vinyl chloride. 

Reactions in various alkyl halide solvents. A preliminary survey of polymerisations catalysed by titanium tetrachloride in various alkyl halide solvents was undertaken using highly purified materials and a vacuum technique. The most important qualitative result obtained was that in the solvents methylene dichloride, ethyl chloride, ethylene dichloride,... 

Synonyms AI3-01656 1,2-Bichloroethane Borer sol BRN 605264 Brocide Caswell No. 440 CCRIS 225 1,2-DCA 1,2-DCE Destruxol borersol Dichloremulsion 1,2-Dichlorethane Dichlormulsion a,p-Dichloroethane sjm-Dichloroethane Dichloroethylene Dutch liquid Dutch oil EDC EINECS 203-458-1 ENT 1656 EPA pesticide chemical code 042003 Ethane dichloride Ethene dichloride Ethylene chloride Ethylene dichloride 1,2-Ethylene dichloride Freon 150 Glycol dichloride HCC 150 NC1-C00511 RCRA waste number U077 UN 1184. 

Chlorinated ethanes and ethylenes comprise ethyl chloride, ethylene dichloride (1,2 dichloroethane), vinyl chloride, trichloroethylene (TCE), perchloroethylene (RCE), and several CFCs. Some of the major uses of these compounds are as degreasing agents, dry-cleaning solvents, building blocks for manufacturing of polymers (e.g., RVC, ethyl cellulose), and raw material for the production of tetraethyl lead and CECs. We discuss ethylene dichloride, trichloroethylene, and perchloroethylene as examples of this group. 

Picryl chloride, Ethylene dichloride, Copper powder, Acetone... 

Nitric acid. Ammonium nitrate, Paraformaldehyde, Hexamine, Acetone, Acetic acid, Acetic anhydride Picryl chloride, Ethylene dichloride, Copper powder, Acetone... 

The gaseous products formed on thermal decomposition of ethylene-platinous chloride are ethylene, hydrogen chloride, vinyl chloride, ethyl chloride, ethylene dichloride and ethylidine dichloride. The half life for the decomposition at 130° is 4.5 days, at 172° it is 1.7 hours 98). The hydrolysis of Zeisc s salt K[PtCl3(C2H4)] by water and dilute acids has been studied ... 

Benzene, toluene, ethyl benzene, xylenes, TCE, chloroform, vinyl chloride, ethylene dichloride, methylene chloride, perchlorofluorocarbons, hexane... 

Synonym ethylene chloride, ethylene dichloride, glycol dichloride, sym-dichloroethane, Dutch oil, EDC... 

The simplest and therefore most probable case of this association of two carbon atoms is that in which one unit of affinity of the one carbon atom is combined with one unit of affinity of the other. Of the 2x4 units of affinity of the two carbon atoms, two are used in holding the two atoms together there remain, therefore, six which may be held in combination by atoms of other elements. In other words the group of two carbon atoms, is hexatomic it will form a compound with 6 atoms of a monatomic element, or in general with that number of atoms that will make the sum of their chemical [affinity, TransL] units=6 (e.g. ethyl hydride, ethyl chloride, ethylene dichloride, l carbon tetrachloride [C2Cle, TransL] j acetonitrile, cyanogen, acetaldehyde, acetyl chloride, glycolide, etc.). 

Use Manufacture of carbon tetrachloride, trichloroethylene, chlorinated hydrocarbons, polychloro-prene (neoprene), polyvinyl chloride, hydrogen chloride, ethylene dichloride, hypochlorous acid, metallic chlorides, chloracetic acid, chlorobenzene, chlorinated lime water purification, shrinkproofing wool, flame-retardant compounds, special batteries (with lithium or zinc) processing of meat, fish, vegetables, and fruit. For information, refer to the Chlorine Institute, 2001 L St., NW, Suite 506, Washington DC 20036. 

Propyl Chloride Ethylene Dichloride Propylene Dichloride... 

Many by-products appear during this conversion, which takes place between 450 and550°C. at about 1.id6 Pa absolute. These by-products include ethyl chloride, ethylene dichloride, ethylene, carbon dioxide, etc. Hence the molar selectivity for vinyl chloride ranges between 65 and 70 per cent m rclationto -ethane and 50 per cent in relation to chlorine, for once-through conversions of 50 and 100 per cent respectively. 

Chlorination of Ethanol. Ethyl alcohol either absolute or containing water is chlorinated to form the hemiacetal of trichloroacetaldehyde from which chloral is liberated by treatment with concentrated sulfuric acid. Ferric chloride may be employed as a chlorination catalyst, but its use does not appear necessary. Five moles of hydrogen chloride is liberated for each mole of chloral produced, and the other by-products include ethyl chloride, ethylene dichloride, and ethyl ether. 

The phosphonium iodides form addition products with the iodides of mercury, bismuth and thallium, and also vdth bismuth chloride. Perhalides, R PI.Xg, are formed when halogens react with the iodides, these products, like the original iodides, having well-defined crystalline forms moist silver oxide removes the iodine, gnung the corresponding hydroxides. Like the arsonium chlorides the tetra-alkylphosphonium chlorides tend to be deliquescent, but they yield crystalline double salts vdth the chlorides of gold, mercury, platinum, bismuth and zinc. When two molecular equivalents of triethylphosphine react with one molecular equivalent of methylene chloride, ethylene dichloride or ethylene dibromide, phosphonium compounds result in which two atoms of phosphorus are present. 

The organic dihalides most often used are those that are commercially available such as methylene chloride, ethylene dichloride, propylene di-chloride, glycerol dichlorohydrin, dichloroethyl ether, dichloroethylformal, and triglycol dichloride. The most reactive chloro-compounds are the primary ones and these are the most commonly used. 

Polystyrene Methylene chloride, ethylene dichloride, trichloroethylene, methyl ethyl ketone, xylene... 

Methylene chloride, ethylene dichloride, and trichloroethylene are some of the fast-drying solvents that produce strong joints. However, they are unsatisfactory for transparent articles of polystyrene because they cause rapid crazing. Medium-drying solvents such as toluene, perchloroethylene, and ethyl benzene that have higher boiling temperature are less apt to cause crazing. 

CAS-No [107-06-2] ethane dtehlorlde ethylene chloride ethylene dichloride 1 -elhylene dichloride... 

Solvents of high polarity are desirable for solvation of ions. However they cannot be employed for ionic polymerizations. Thus highly polar hydroxylic solvents, such as water and alcohols, react with and destroy most ionic initiators and propagating species. Other polar solvents such as ketones form highly stable complexes with initiators, thus preventing initiation reactions. Most ionic polymerizations are, therefore, carried out in low or moderately polar solvents such as methyl chloride, ethylene dichloride, and pentane. 

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