Acid precipitation sulfur

Salicylic acid Precipitated sulfur Hydrophilic ointment... 

Dilute acids precipitate sulfur from thiosulfates (difference from sulfides and sulfites),... 

Because of the mixture of VOCs in the atmosphere, the composition of smog reaction products and intermediates is extremely complex. formed via reaction 16, is important because when dissolved in cloud droplets it is an important oxidant, responsible for oxidising SO2 to sulfuric acid [7664-93-9] H2SO4, the primary cause of acid precipitation. The oxidation of many VOCs produces acetyl radicals, CH CO, which can react with O2 to produce peroxyacetyl radicals, CH2(C0)02, which react with NO2... 

Metallic Dyes. MetaUic dyes are among the older hair color materials known. Commercial products are based on a 1% solution of lead acetate in an aqueous, slightly acidic, alcohoHc medium. Precipitated sulfur appears to be essential. The convenience aspect is stressed by the leave-in appHcation method. Actually, the color development is so slow, taking about a week to ten days, that there is no alternative to this technique. Daily appHcation is needed at first. 

Arsenates are oxidizing agents and are reduced by concentrated hydrochloric acid or sulfur dioxide. Treatment of a solution of orthoarsenate with silver nitrate in neutral solution results in the formation of a chocolate-brown precipitate of silver orthoarsenate, Ag AsO, which may be used as a test to distinguish arsenates from phosphates. With hydrofluoric acid, orthoarsenate solutions yield hexafluoroarsenates, eg, potassium hexafluoroarsenate [17029-22-0] (KAsFg)2 H2O. Arsenates of calcium or lead are used as insecticides sodium arsenate is used in printing inks and as a mordant. 

Arsenic pentasulfide (arsenic(V) sulfide), As S q, is stable in air up to 95°C, but at higher temperatures begins to dissociate into arsenous sulfide and sulfur. It is prepared by the fusion of arsenic with sulfur foUowed by extraction with ammonia and reprecipitation at low temperatures by addition of hydrochloric acid. Arsenic pentasulfide is precipitated at low temperatures from strongly acidic arsenate solutions by a rapid stream of hydrogen sulfide. It is hydrolyzed by boiling with water, yielding arsenous acid and sulfur. Salts derived from a number of thioarsenic acids are formed from arsenic pentasulfide and alkaH metal sulfides. 

Some products are precipitated from the fermentation broth. The insoluble calcium salts of some organic acids precipitate and are col-lec ted, and adding sulfuric acid regenerates the acid while forming gypsum (calcium sulfate) that constitutes a disposal problem. An early process for recovering the antibiotic cycloserine added silver nitrate to the fermentation broth to precipitate an insoluble silver salt. This process was soon obsolete because of poor economics and because the silver salt, when diy, exploded easily. 

The chemistry of such solutions has been alluded to on p. 678. At low temperatures a hydrate H28.5IH2O crystallizes. In acid solution H28 is also a mild reducing agent e.g. even on standing in air solutions slowly precipitate sulfur. The gas bums with a bluish flame in air to give H2O and 8O2 (or H2O and 8 if the air supply is restricted). For adducts, see p. 673. 

Land/atmospheric interfacial processes which impact climate and biological activity on earth are illustrated in Figure 3. Emissions of carbon dioxide, methane, nitrogen dioxide, and chlorofluorocarbons (CFCs) have been linked to the transmission of solar radiation to the surface of the earth as well as to the transmission of terrestrial radiation to space. Should solar radiation be an internal process or an external driver of the hydrologic cycle, weather, and air surface temperatures Compounds of sulfur and nitrogen are associated with acidic precipitation and damage to vegetation, aquatic life, and physical structures. 

Irving, P. Ed. Acidic deposition State of science and technology. National Acid Precipitation Assessment Program, Washington, DC, 1990. Clark, T.L., Denise, R.L., Seilhop, S.K., Voldner, E.C., Olson, M.P., and Alvo, M. International sulfur desposition model evaluation. Atmospheric Environment Service, Publication No. ARD-87-1, 1987, Downsview, Ontario, Canada. 

HO and Acid Precipitation. Hydroxyl radical is also active in the transformations of the key nitrogen and sulfur species that dominate acidified precipitation ... 

Acid precipitation, or acid rain, can causes significant impacts on freshwater, coastal, and forested ecosystems (e.g.. Likens et ai, 1996). Both NOi", from NO emissions, and SO from SO2 emissions contribute significantly to acid rain. The relative ratio of SO /NOf in precipitation will be substantially determined by the regional emissions of SO2/NO3. In developed countries, uncontrolled combustion of coal and high-sulfur fuel oil led to significant emissions of SO2, relative to NO Due to strict control of smokestack SO2 emissions in some regions and increasing NO emissions from automobiles, the relative contribution of NOi is expected to increase (Sirois, 1993 Mayewski et ai, 1990). 

Acid rain is actually a catchall phrase for any kind of acidic precipitation, including snow, sleet, mist, and fog. Acid rain begins when water comes into contact with sulfur and nitrogen oxides in the atmosphere. These oxides can come from natural sources such as volcanic emissions or decaying plants. But there are man-made sources as well, such as power plant and automobile emissions. In the United States, two-thirds of all the sulfur dioxide and one-fourth of the nitrogen oxides in the atmosphere are produced by coal-burning power plants. 

Zakshek EM, Puckett KJ, Percy KE. 1986. Lichen sulfur and lead levels in relation to deposition patterns in Eastern Canada. International Symposium on Acidic Precipitation, Muskoka. Ontario, Canada, Sept. 15-20,1985. Water Air Soil Pollut 30 161-169. 

The resulting products, such as sulfenic acid or sulfur dioxide, are reactive and induce an acid-catalyzed breakdown of hydroperoxides. The important role of intermediate molecular sulfur has been reported [68-72]. Zinc (or other metal) forms a precipitate composed of ZnO and ZnS04. The decomposition of ROOH by dialkyl thiophosphates is an autocata-lytic process. The interaction of ROOH with zinc dialkyl thiophosphate gives rise to free radicals, due to which this reaction accelerates oxidation of hydrocarbons, excites CL during oxidation of ethylbenzene, and intensifies the consumption of acceptors, e.g., stable nitroxyl radicals [68], The induction period is often absent because of the rapid formation of intermediates, and the kinetics of decomposition is described by a simple bimolecular kinetic equation... 

Amino Acid Content. Amino acid content of field pea products is related to protein level, method of processing, and fraction (starch or protein). The protein fraction contains fewer acidic (glu, asp) amino acids than the starch fraction and more basic (lys, his, arg) amino acids than the starch fraction. Also, there are more aromatic (tyr, phe) amino acids, leu, iso, ser, val, and pro in the protein fraction than in the starch fraction (5). An amino acid profile of pea protein concentrate shows relatively high lysine content (7.77 g aa/16 g N) but low sulfur amino acids (methionine and cystine) (1.08-2.4 g aa/16 g N). Therefore, it is recommended that air classification or ultrafiltration be used because acid precipitation results in a whey fraction which contains high levels of sulfur amino acids (12,23). Also, drum drying sodium proteinates decreases lysine content due to the Maillard reaction (33). 

Dissolving the crude product, for instance in sulfuric acid, precipitation in water and/or organic solvents, possibly in the presence of surfactants at exactly defined conditions. 

Methane releases 25% less carbon dioxide per gram than coal, and it emits none of the oxides of nitrogen and sulfur that contribute to acid precipitation. Therefore, using methane in place of other fossil fuels is very desirable. Methane hydrates seem to be an ideal and plentiful pre-packaged source of natural gas. Estimates of the exact amount of methane stored in hydrates suggest there could be... 

In order to ensure a consistent supply of coal for steam generation, plants typically maintain an outdoor 90-day reserve supply. The pUes are usually not enclosed, so the coal comes in contact with moisture and air, which can oxidize metal sulfides to sulfuric acid. Precipitation then results in coal pile runoff with minerals, metals, and low pH (occasionally) in the stream. 

Detergents are like soaps, but they re derivatives of either phosphoric acid or sulfuric acid (see Figure 16-31). They ve gained popularity laecause they don t precipitate in hard water. 

Extraction is commonly carried out by hydrolysis in boiling acid such as chloridric acid or sulfuric acid. To release thiamine bonded to phosphate enzyme, hydrolysis with phosphatase, alone or together with claradiastase or takadiastase, is carried out. After the enzymatic digestion, an acid treatment is applied in order to precipitate the protein and denaturate the enzymes. Ndaw et al. [603] proved that for extraction of vitamins Bj, B, and Bg, acid hydrolysis is always superfluous if the activity of the enzymes chosen is sufficiently high. SPE or column chromatography may be used in further purification, mainly to remove excess of derivatization reagents used to convert thiamine to a highly flnorescent thiochrome derivatives. lEC may be used in purification step, as well. 

Drugs that are used to treat hyperkeratosis, a thickening of the stratum corneum, are called keratolytics. Examples of these agents are salicylic acid, urea, lactic acid, and colloidal or precipitated sulfur. The precise mechanisms by which these agents treat hyperkeratosis are not known. Presumably, a common property is the ability to denature keratin, the major structural protein of the epidermis. Other beneficial effects vary among the different drugs. All of them have antimicrobial or... 

Calvert, J. G., and W. R. Stockwell, Mechanism and Rates of the Gas Phase Oxidations of Sulfur Dioxide and Nitrogen Oxides in the Atmosphere, in S02, NO and N02 Oxidation Mechanisms Atmospheric Considerations (J. G. Calvert, Ed.), Acid Precipitation Series, Vol. 3, pp. 1-62 (J. I. Teasley, Series Editor), Butterworth, Stoneham, MA, 1984. 

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