Chlorine solvents for

Uses Solvent for chlorinated rubber insecticide and bleach manufacturing paint, varnish and rust remover manufacturing degreasing, cleansing, and drying of metals denaturant for ethyl alcohol preparation of 1,1-dichloroethylene extractant and solvent for oils and fats insecticides weed killer fumigant intermediate in the manufacturing of other chlorinated hydrocarbons herbicide. 

As an example, the self-ignition of gas phase mixtures of dioxane and chlorine was thoroughly investigated by F. Battin-Leclerc (refs. 10, 11). Dioxane is sometimes mentioned as a solvent for chlorination processes (ref. 12) whereas selfignitions of dioxane + chlorine mixtures is easily obtained near the ambient temperature. 

MAJOR USES Used in manufacture of 1,1-dichloroethene used as a solvent for chlorinated rubbers, oils, waxes, fats and resins used in organic synthesis. 

ORIGIN/INDUSTRY SOURCES/USES organic chemical industry, solvent for chlorinated rubber and other organic materials paint varnish rust remover soil fumigant cleansing and degreasing metals photo films resins and waxes extracant for oils and fats herbicide alcohol denaturant... 

A liquid solvent for chlorine is poured into a flask in which the following reaction is at equilibrium ... 

Uses Refrigerants metal degreasing agric. fumigant chlorinating organic compds. production of semiconductors solvent for fats, oils, rubber, pharmaceuticals solvent for chlorination reactions Use Level 4 ppm (pharmaceuticals)... 

Water is an inefficient solvent for chlorine (Section 7.5.9.1), but there are potential flowsheet efficiencies in some plants. A plant that uses direct-contact cooling in the main chlorine train can also absorb chlorine from the tail gas in cold water. The solution produced in this step may be used in the cooling process in any event the absorbed chlorine is released in the steam stripper that handles the water from the cooling system. The recovered chlorine then has another pass through the recovery system, while the inert gases are vented from the tail gas absorber. 

Chlorine is readily soluble in sulfiir-chlorine compounds, which can be used as industrial solvents for chlorine. Disulfiir dichloride U0025-67-9], S2CI2, is converted to sulfur dichloride (SCI2) and sulfiir tetrachloride (SCI4). Some metallic chlorides and oxide chlorides, such as vanadium oxide chloride, chromyl chloride, titanium tetrachloride, and tin(IV) chloride, are good solvents for chlorine. Many other chlorine-containing compounds dissolve chlorine readily. Examples are phosphoryl chloride, carbon tetrachloride (Fig. 7), tetrachloroethane, pentachloroethane, hexachlorobutadiene... 

The more complex the polymer, the stronger is the solvent required to dissolve it. White spirit is suitable for oil and alkyd resins, and toluene is a good solvent for chlorinated rubber as it has higher solvent power. 

CH2C1 CH2C1. Colourless liquid with an odour like that of chloroform b.p. 84 C. It is an excellent solvent for fats and waxes. Was first known as oil of Dutch chemists . Manufactured by the vapour- or liquid-phase reaction of ethene and chlorine in the presence of a catalyst. It reacts with anhydrous ethano-ales to give ethylene glycol diethanoate and with ammonia to give elhylenediamine, these reactions being employed for the manufacture of these chemicals. It burns only with difficulty and is not decomposed by boiling water. 

CH2CI2. A colourless liquid with a chloroform-like odour b.p. 4I°C. Prepared by heating chloroform with zinc, alcohol and hydrochloric acid manufactured by the direct chlorination of methane. Decomposed by water at 200°C to give methanoic and hydrochloric acids. Largely used as a solvent for polar and non-polar substances, particularly for paint removal (30%), dissolving cellulose acetate and degreasing (10%). It is more stable than carbon tetrachloride or chloroform especially towards moisture or alkali. It is somewhat toxic. U.S. production 1981 280000 tonnes. 

Uses. Tetrahydrofurfuryl alcohol is of interest in chemical and related industries where low toxicity and minimal environmental impact are important (134). For many years tetrahydrofurfuryl alcohol has been used as a specialty organic solvent. The fastest growing appHcations are in formulations for cleaners (135) and paint strippers (136), often as a replacement for chlorinated solvents (137). Other major appHcations include formulations for crop sprays, water-based paints, and the dyeing and finishing of textiles and leathers. Tetrahydrofurfuryl alcohol also finds appHcation as an intermediate in pharmaceutical appHcations. 

Acetonitrile also is used as a catalyst and as an ingredient in transition-metal complex catalysts (35,36). There are many uses for it in the photographic industry and for the extraction and refining of copper and by-product ammonium sulfate (37—39). It also is used for dyeing textiles and in coating compositions (40,41). It is an effective stabilizer for chlorinated solvents, particularly in the presence of aluminum, and it has some appflcation in... 

Most solvents for hydroperoxides are not completely inert to radical attack and, consequendy, react with radicals from the hydroperoxide to form solvent-derived radicals, either by addition to unsaturated sites or by hydrogen- or chlorine-atom abstraction. In equation 15, S—H represents solvent and S is a solvent radical. 

The most innovative photohalogenation technology developed in the latter twentieth century is that for purposes of photochlorination of poly(vinyl chloride) (PVC). More highly chlorinated products of improved thermal stabiUty, fire resistance, and rigidity are obtained. In production, the stepwise chlorination may be effected in Hquid chlorine which serves both as solvent for the polymer and reagent (46). A soHd-state process has also been devised in which a bed of microparticulate PVC is fluidized with CI2 gas and simultaneously irradiated (47). In both cases the reaction proceeds, counterintuitively, to introduce Cl exclusively at unchlorinated carbon atoms on the polymer backbone. 

Solubility. Poly(ethylene oxide) is completely soluble in water at room temperature. However, at elevated temperatures (>98° C) the solubiUty decreases. It is also soluble in several organic solvents, particularly chlorinated hydrocarbons (see Water-SOLUBLE polymers). Aromatic hydrocarbons are better solvents for poly(ethylene oxide) at elevated temperatures. SolubiUty characteristics are Hsted in Table 1. 

Solubility. Cross-linking eliminates polymer solubiUty. Crystallinity sometimes acts like cross-linking because it ties individual chains together, at least well below T. Thus, there are no solvents for linear polyethylene at room temperature, but as it is heated toward its (135°C), it dissolves in a variety of aUphatic, aromatic, and chlorinated hydrocarbons. A rough guide to solubiUty is that like dissolves like, ie, polar solvents tend to dissolve polar polymers and nonpolar solvent dissolve nonpolar polymers. 

DAG is treated with ethanol and hydrochloric acid in the presence of inert solvent, eg, chlorinated solvents, hydrocarbons, ketones, etc. The L-ascorbic acid precipitates from the mixture as it forms, minimising its decomposition (69). Cmde L-ascorbic acid is isolated through filtration and purified by recrystallization from water. The pure L-ascorbic acid is isolated, washed with ethanol, and dried. The mother Hquor from the recrystallization step is treated in the usual manner to recover the L-ascorbic acid and ethanol contained in it. The cmde L-ascorbic acid mother Hquor contains solvents and acetone Hberated in the DAG hydrolysis. The solvents are recovered by fractional distillation and recycled. Many solvent systems have been reported for the acid-catalyzed conversion of DAG to L-ascorbic acid (46). Rearrangement solvent systems are used which contain only the necessary amount of water required to give >80% yields of high purity cmde L-ascorbic acid (70). 

Polystyrene. Polystyrene [9003-53-6] is a thermoplastic prepared by the polymerization of styrene, primarily the suspension or bulk processes. Polystyrene is a linear polymer that is atactic, amorphous, inert to acids and alkahes, but attacked by aromatic solvents and chlorinated hydrocarbons such as dry cleaning fluids. It is clear but yellows and crazes on outdoor exposure when attacked by uv light. It is britde and does not accept plasticizers, though mbber can be compounded with it to raise the impact strength, ie, high impact polystyrene (HIPS). Its principal use in building products is as a foamed plastic (see Eoamed plastics). The foams are used for interior trim, door and window frames, cabinetry, and, in the low density expanded form, for insulation (see Styrene plastics). 

A significant use of butylene oxide [26249-20-7] is as an acid scavenger for chlorine-containing materials such as trichloroethylene. Inclusion of about 0.25—0.5% of butylene oxide, based on the solvent weight, during preparation of vinyl chloride and copolymer resin solutions minimizes container corrosion which may be detrimental to resin color and properties. 

The physical properties of methylene chloride are Hsted in Table 1 and the binary a2eotropes in Table 2. Methylene chloride is a volatile Hquid. Although methylene chloride is only slightly soluble in water, it is completely miscible with other grades of chlorinated solvents, diethyl ether, and ethyl alcohol. It dissolves in most other common organic solvents. Methylene chloride is also an excellent solvent for many resins, waxes, and fats, and hence is well suited to a wide variety of industrial uses. Methylene chloride alone exhibits no dash or fire point. However, as Htde as 10 vol % acetone or methyl alcohol is capable of producing a dash point. 

Carbon tetrachloride [56-23-5] (tetrachloromethane), CCl, at ordinary temperature and pressure is a heavy, colorless Hquid with a characteristic nonirritant odor it is nonflammable. Carbon tetrachloride contains 92 wt % chlorine. When in contact with a flame or very hot surface, the vapor decomposes to give toxic products, such as phosgene. It is the most toxic of the chloromethanes and the most unstable upon thermal oxidation. The commercial product frequendy contains added stabilizers. Carbon tetrachloride is miscible with many common organic Hquids and is a powerhil solvent for asphalt, benzyl resin (polymerized benzyl chloride), bitumens, chlorinated mbber, ethylceUulose, fats, gums, rosin, and waxes. 

Trichloroethane and other chlorinated solvents are used for vapor degreasing (84—90). Other uses include cold metal cleaning, printed ckcuit board cleaning, and as a solvent for inks, coatings, adhesives, and aerosols. 1,1,1-Trichloroethane is an excellent solvent for development of photoresist polymers used in printed ckcuit board manufacture (see Integrated circuits Photoconductivepolymers). 

The principal use of 1,1,2-trichloroethane is as a feedstock intermediate in the production of 1,1-dichloroethylene. 1,1,2-Trichloroethane is also used where its high solvency for chlorinated mbbers, etc, is needed, as a solvent for pharmaceutical preparation, and in the manufacture of electronic components. 

Tetrachloroethane [79-34-5] acetylene tetrachloride, CHCI2CHCI2, is a heavy, nonflammable Hquid with a sweetish odor. It is miscible with the chlorinated solvents and shows high solvency for a number of natural organic materials. It is also a solvent for sulfur and a number of inorganic compounds, eg, sodium sulfite. 

Dichloroethylene can be used as a low temperature extraction solvent for organic materials such as dyes, perfumes, lacquers, and thermoplastics (13—15). It is also used as a chemical intermediate in the synthesis of other chlorinated solvents and compounds (2). 

Special additives are often included in a carrier formulation to provide specific properties such as foam control, stabiUty, and fiber lubrication during dyeing. Most important are the solvents used to solubilize the soHd carrier-active chemicals. These often contribute to the general carrier activity of the finished product. For example, chlorinated benzenes and aromatic esters are good solvents for biphenyls and phenylphenols. Flammable compounds (flash point below 60°C) should be avoided. 

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