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Degradation Degreasing

Most of the trichloroethylene used in the United States is released into the atmosphere by evaporation primarily from degreasing operations. Once in the atmosphere, the dominant trichloroethylene degradation process is reaction with hydroxyl radicals the estimated half-life for this process is approximately 7 days. This relatively short half-life indicates that trichloroethylene is not a persistent atmospheric compound. Most trichloroethylene deposited in surface waters or on soil surfaces volatilizes into the atmosphere, although its high mobility in soil may result in substantial percolation to subsurface regions before volatilization can occur. In these subsurface environments, trichloroethylene is only slowly degraded and may be relatively persistent. [Pg.202]

NPE was previously used extensively as nonionic surfactants and emulsifiers in both the textile and the leather industry but has now been replaced by alternative surfactants in Europe. The main alternatives in the leather industry are linear alcohol ethoxylates with different chain lengths and ethoxylation degrees. These compounds are much easier than NPE degraded to non-toxic compounds. The efficiency of linear alcohol ethoxylates as degreasing agents is comparable to that of NPE. [Pg.260]

Degradation of agrochemicals, solvents, degreasers, flame retardants, and chemical intermediates used in the production of high volume chemicals [113] detoxification of chlorophenols [61] Transformation of pesticides including phenylcarbamates (e.g., CIPC, IPQ and organophosphates (e.g., malathion, paraoxon, parathion) [53]... [Pg.435]

Normal trichlorethylene degreasing has no effect on zinc or zinc-aluminum alloys, provided immersion in solution that has become degraded or contaminated is avoided. [Pg.376]

Water washing drilling mud from a plugged tower Acidize/degrease trays Reestablished liquid seal Foaming of degraded glycol... [Pg.488]

Steel grit should not be used on non-ferrous metals as it will leave a ferrous smudge that can later oxidise and degrade the bond. After blasting, it is recommended to use either solvent degreasing or alkaline cleaning on the metal a second time to remove dust and any other particulate byproducts from the blasting process. [Pg.68]


See other pages where Degradation Degreasing is mentioned: [Pg.545]    [Pg.122]    [Pg.256]    [Pg.471]    [Pg.208]    [Pg.349]    [Pg.41]    [Pg.59]    [Pg.156]    [Pg.111]    [Pg.1845]    [Pg.65]    [Pg.158]    [Pg.654]    [Pg.657]    [Pg.455]    [Pg.390]    [Pg.192]    [Pg.506]    [Pg.43]    [Pg.5063]    [Pg.7161]    [Pg.1571]    [Pg.412]    [Pg.1819]    [Pg.37]    [Pg.1571]    [Pg.41]    [Pg.734]    [Pg.251]    [Pg.20]    [Pg.847]    [Pg.303]    [Pg.369]    [Pg.326]    [Pg.326]    [Pg.542]    [Pg.108]    [Pg.5]    [Pg.67]    [Pg.88]    [Pg.205]    [Pg.277]   
See also in sourсe #XX -- [ Pg.33 ]




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