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Vinyl chloride, escape

For the next five hours, 670 tons (608,000 kg) of vinyl chloride escaped from the sphere, which was under about 30 psig (2.4 bar) pressure. The discharging liquid jetted out selfrefrigerated and froze the water that was being poured over the sphere. Engineers determined that liquid vinyl chloride escaped at about 3500 liters/min (725 gal/min). [Pg.97]

The Occupational Safety and Health Administration (OSHA) has set the permissible exposure level (PEL) of vinyl chloride (VC) at 1.0 part per million (ppm) as a maximiun time-weighted average (TWA) for an 8-h workday. The PEL was set at 1.0 ppm because vinyl chloride is a suspected carcinogen. Thus, if vinyl chloride escapes into the air, the concentration of vinyl chloride must be maintained at or below 1.0 ppm. The major source of VC escape into the workplace air in typical process conditions is fugitive emissions from pipe connections such as valves, flanges, and pump seals. [Pg.767]

Before distilling checkfor peroxides if found, render harmless. Depending on the degree ofexposure.regularmedicalcheckups are advisable. Turn leaking cylinder so that leak is on top to prevent liquid vinyl chloride escaping. ... [Pg.918]

Escaping vinyl chloride vapor, liquid and mist... [Pg.103]

Out of the many chlorinated derivatives, vinyl chloride has been a focus of interest since its carcinogenic effects were discovered. Approximately 6% of its world production is assumed to escape into the atmosphere. Vinyl chloride is used for the production of different plastics and methylchloro-form, and it is added to mixtures for the production of special packing materials. Until recently it has been used as a medium in aerosol sprays. The imission concentrations in the vicinity of production sources (0 to 8 km) are generally below 2.6 ng m. In the literature, there are only few data about its atmospheric reactions. It is very probable that it participates in photooxidation reactions in the presence of nitrogen oxides. Carbon monoxide formaldehyde, formic acid and HCl are products of its photooxidation. [Pg.498]

The expanding vinyl chloride market helped industry to escape from inclined production. [Pg.282]

PVC is produced by polymerization of vinyl chloride by free-radical mechanisms, mainly in suspension and emulsion, but bulk and solution processes are also employed to some extent [11-14]. (The control of vinyl chloride monomer escaping into the atmosphere in the PVC production plant has become important because cases of angiosarcoma, a rare type of liver cancer, were found among workers exposed to the monomer. This led to setting of stringent standards by governments and modification of manufacturing processes by the producers to comply with the standards.)... [Pg.396]

To a 1-L three-necked flask equipped with condenser, thermometer and gas inlet tube were added 300 mL thiophene-free benzene and 50 g AICI3. The solution was agitated using a stirrer at 1000-1400 rpm until the aluminum chloride was in a flnely divided state. Then vinyl chloride gas was passed into the flask at such a rate that only a few bubbles of gas escaped from an alkali trap connected to the condenser. The reaction was kept at 0-5°C. No hydrogen chloride was evolved until an initial period of 15-20 min. [Pg.92]

Substances that have terminal double or triple bonds, if unconjugated to other multiple bonds, are oxidized by P-450 in the e.r. to toxic substances which attack this porphyrin and deactivate it. Examples are ethylene, acetylene, vinyl chloride and the hypnotic ethchlorvynol which is l-chloro-3-ethylpent-l-en-4-yn-3-ol. Thus, ethylene leads to the A-2-hydroxyethy 1-derivative of P-450. A further adverse effect is that other drugs, if given at the same time, escape the usual metabolic transformation and so build up in the patient (Ortiz de Montellano, Beilan and Matthews, 1982). [Pg.106]

Vinyl chloride y 1 2.3 hazardous escape only 25 unlimited... [Pg.674]

A Smith-Ewart case 1 behavior in 1) can be observed during emulsion polymerization of monomers with a high chain-transfer rate constant such as vinyl chloride because the monomer radicals have a high tendency to escape from the particles. Especially for vinyl chloride emulsion polsunerization, Ugelstad and Hansen (113) derived the following equation 18 to calculate n, which predicts dependence, h a... [Pg.3699]

In the reaction ol t biiiylniagnesium chloride with benzophenone. escaped /-butyl radicals rettcl by clisproporttotiiiiioti foriiting isobulane ami isobutene. CIDNP signals were observed lor the vinylic protons ol isobutene 72. ... [Pg.16]


See other pages where Vinyl chloride, escape is mentioned: [Pg.553]    [Pg.103]    [Pg.62]    [Pg.95]    [Pg.102]    [Pg.432]    [Pg.497]    [Pg.347]    [Pg.348]    [Pg.431]    [Pg.46]    [Pg.160]    [Pg.183]    [Pg.56]   
See also in sourсe #XX -- [ Pg.90 , Pg.94 , Pg.95 , Pg.96 ]




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