Solvent, solvents 1,1,1-trichloroethane

Vinyl chloride is produced in the following industrial reactions (1) the thermal cracking of 1,2-dichlor-oethane, which is produced by the chlorination and/ or oxychlorination of ethylene and (2) the hydrochlorination of acetylene. The vast majority of vinyl chloride is used for the production of polyvinyl chloride (PVC) and the manufacture of copolymers with monomers such as vinyl acetate or vinylidene chloride. A much smaller proportion of vinyl chloride is used in the production of chlorinated solvents - primarily trichloroethanes. 

The alkaloids were extracted into ethanol and purified on a column chromatography of diatomaceous earth moistened with 2.5 H H2 SO. Non-alkaloidal materials were first eluted with ethylether, alkaloids were then eluted with CHCI3 saturated with aqueous ammonia. After evaporation of eluate, a solution of the residue in chloroform was submitted to TLC plates of silica gel 60 F-254 which developed in the solvent trichloroethane-diethylamine (9 1). After drying at 105 for 2 hours, the plates were sprayed with a solution of 4-dimethylaminobenzaldehyde in ethanol-4 M H2SO4 (1 1) and again dried at 105" for 60 minutes. Hyoscyamine and scopolamine spots were determined with the use of high-speed scanner at 495 nm. The calibration graph was rectilinear for 0.2 to 2.0 mg ml"1 of alkaloid, and the detection limit was 50 ng. The method was rapid and comparable with... 

Solvent 111. See 1,1,1-Trichloroethane 142 Solvent 66/3. See Stoddard solvent Solvent 170. See Petroleum distillates, hydrotreated light... 

Numerous studies are underway to find surface treatment methods that minimize or eliminate use of toxic materials or polluting substances. Some progress is being made, " but replacement of such degreasing solvents as trichloroethane and such toxic materials as the dichromates will take time. For polymeric surfaces, plasma or corona discharge treatments are receiving much attention. 

Lipase and others Activated PEG2 Effect of water and solvent Benzene, trichloroethane, dimethylsulfoxide 59, 67, 68... 

The performance of SCWO for waste treatment has been demonstrated (15,16). In these studies, a broad number of refractory materials such as chlorinated solvents, polychlorinated biphenyls (PCBs), and pesticides were studied as a function of process parameters (17). The success of these early studies led to pilot studies which showed that chlorinated hydrocarbons, including 1,1,1-trichloroethane /7/-T5-6y,(9-chlorotoluene [95-49-8] and hexachlorocyclohexane, could be destroyed to greater than 99.99997, 99.998, and 99.9993%, respectively. In addition, no traces of organic material could be detected in the gaseous phase, which consisted of carbon dioxide and unreacted oxygen. The pilot unit had a capacity of 3 L/min of Hquid effluent and was operated for a maximum of 24 h. 

Finally, nitromethane has been used in large quantities as a stabilizer for 1,1,1-trichloroethane. The use of this degreasing solvent is expected to decHne and disappear under the provisions of the Montreal Protocol (116), which bans ozone-depleting substances, of which this is one. 

SolubiHty of the three commercial polysulfones foUows the order PSF > PES > PPSF. At room temperature, all three of these polysulfones as weU as the vast majority of other aromatic sulfone-based polymers can be readily dissolved in a few highly polar solvents to form stable solutions. These solvents include NMP, DMAc, pyridine, and aniline. 1,1,2-Trichloroethane and 1,1,2,2-tetrachloroethane are also suitable solvents but are less desirable because of their potentially harmful health effects. PSF is also readily soluble in a host of less polar solvents by virtue of its lower solubiHty parameter. 

Bitumen Soluble in Carbon Disuffide (ASTMD4). Asphalt is defined as a mixture of hydrocarbons that are completely soluble in carbon disulfide. Trichloroethylene or 1,1,1-trichloroethane have been used in recent years as safer solvents for this purpose. The procedure for these and other solvents for asphalt with Htde or no mineral matter are described in ASTM D2042. 

Chlorination of various hydrocarbon feedstocks produces many usehil chlorinated solvents, intermediates, and chemical products. The chlorinated derivatives provide a primary method of upgrading the value of industrial chlorine. The principal chlorinated hydrocarbons produced industrially include chloromethane (methyl chloride), dichloromethane (methylene chloride), trichloromethane (chloroform), tetrachloromethane (carbon tetrachloride), chloroethene (vinyl chloride monomer, VCM), 1,1-dichloroethene (vinylidene chloride), 1,1,2-trichloroethene (trichloroethylene), 1,1,2,2-tetrachloroethene (perchloroethylene), mono- and dichloroben2enes, 1,1,1-trichloroethane (methyl chloroform), 1,1,2-trichloroethane, and 1,2-dichloroethane (ethylene dichloride [540-59-0], EDC). 

Ninety-six percent of the EDC produced in the United States is converted to vinyl chloride for the production of poly(vinyl chloride) (PVC) (1) (see Vinyl polymers). Chloroform and carbon tetrachloride are used as chemical intermediates in the manufacture of chlorofluorocarbons (CECs). Methjiene chloride, 1,1,1-trichloroethane, trichloroethylene, and tetrachloroethylene have wide and varied use as solvents. Methyl chloride is used almost exclusively for the manufacture of silicone. Vinylidene chloride is chiefly used to produce poly (vinylidene chloride) copolymers used in household food wraps (see Vinylidene chloride and poly(vinylidene chloride). Chloroben2enes are important chemical intermediates with end use appHcations including disinfectants, thermoplastics, and room deodorants. 

Many chlorinated hydrocarbons react readily with aluminum in the so-caHed bleeding reaction. A red aluminum chloride—chlorinated hydrocarbon complex is formed. Storage of uninhibited chlorinated solvents in aluminum vessels results in corrosion in a short period of time. Proprietary organic inhibitors permit commercial use of reactive solvents such as 1,1,1-trichloroethane and trichloroethylene for cleaning of aluminum. 

AH volatile organic solvents are toxic to some degree. Excessive vapor inhalation of the volatile chloriaated solveats, and the central nervous system depression that results, is the greatest hazard for iadustrial use of these solvents. Proper protective equipment and operating procedures permit safe use of solvents such as methylene chloride, 1,1,1-trichloroethane, trichloroethylene, and tetrachloroethylene ia both cold and hot metal-cleaning operations. The toxicity of a solvent cannot be predicted from its chlorine content or chemical stmcture. For example, 1,1,1-trichloroethane is one of the least toxic metal-cleaning solvents and has a recommended threshold limit value (TLV) of 350 ppm. However, the 1,1,2-trichloroethane isomer is one of the more toxic chloriaated hydrocarboas, with a TLV of only 10 ppm. 

Oxidation. Atmospheric oxidation of 1,2-dichloroethane at room or reflux temperatures generates some hydrogen chloride and results in solvent discoloration. A 48-h accelerated oxidation test at reflux temperatures gives only 0.006% hydrogen chloride (22). Addition of 0.1—0.2 wt. % of an amine, eg, diisopropylamine, protects the 1,2-dichloroethane against oxidative breakdown. Photooxidation in the presence of chlorine produces monochloroacetic acid and 1,1,2-trichloroethane (23). 

Trichloroethane [71-55-6] methyl chloroform, CH CCl, is a colorless, non-flammable Hquid with a characteristic ethereal odor. It is miscible with other chlorinated solvents and soluble in common organic solvents. The compound was first prepared by Regnault about 1840. 

Oxidation. 1,1,1-Trichloroethane is stable to oxidation when compared to olefinic chlorinated solvents like trichloroethylene and tetrachloroethylene. Use of a 48-h accelerated oxidation test gave no hydrogen chloride, whereas trichloroethylene gave 0.4 wt % HCl and tetrachloroethylene gave 0.6 wt % HCl (22). 

Entry into a tank that has contained any chlorinated or any easily evaporated solvent requires special procedures to ensure worker safety. The heavier vapors tend to concentrate in unventilated spaces. The proper tank entry procedure requires positive ventilation, testing for residue solvent vapor and oxygen levels, and the use of respiratory equipment and rescue harness. Monitoring the tank from outside is also important. The use of an appropriate gas mask is permissible in vapor concentrations of less than 2% and when there is no deficiency of atmospheric oxygen, but not for exposures exceeding one-half hour. Skin exposure to 1,1,1-trichloroethane can cause irritation, pain, bHsters, and even burning. Eye exposure may produce irritation, but should... 

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). 

Trichloroethane [79-00-5], vinyl trichloride, CH2CICHCI2, is a colorless, nonflammable Hquid with a pleasant odor, miscible with chlorinated solvents, and (as is 1,1,1-trichloroethane) soluble in the other common organic solvents. 

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. 

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