Sulfate metallic hydroxy

G.L. Grandjean, E. (eds.) Mdssbauer spectroscopy applied to inorganic chemistry. Plenum Publ. Corp., 3 417-444 Webb, J. Macey, D.J. Mann, S. (1989) Biomineralization of iron in molluscan teeth. In Mann, S. Webb, J. Williams, R.J.P. (eds.) Biomineralization Chemical and biochemical perspectives. VCH Weinheim, 345-387 Webster, J.G. Swedlund, P.J. Webster, K.S. (1998) Trace metal adsorption onto an acid mine drainage iron(lll) oxy hydroxy sulfate. Environ. Sci.Techn. 32 1361-1368 Wedepohl, K.H. (1969) Composition and abundance of common igneous rocks. In Wedepohl, K.H. (ed.) Handbook of geochemistry. Springer, Berlin, 1 227-249 Wedepohl, K.H. (1969a) Composition and abundance of common sedimentary rocks. 

The exposure of sulfide minerals contained in mine wastes to atmospheric oxygen results in the oxidation of these minerals. The oxidation reactions are accelerated by the catalytic effects of iron hydrolysis and sulfide-oxidizing bacteria. The oxidation of sulfide minerals results in the depletion of minerals in the mine waste, and the release of H, SO4, Fe(II), and other metals to the water flowing through the wastes. The most abundant solid-phase products of the reactions are typically ferric oxyhydroxide or hydroxysulfate minerals. Other secondary metal sulfate, hydroxide, hydroxy sulfate, carbonate, arsenate, and phosphate precipitates also form. These secondary phases limit the concentrations of dissolved metals released from mine wastes. 

Webster J. G., Swedlund P. J., and Webster K. S. (1998) Trace metal adsorption onto an acid drainage iron(III) oxy hydroxy sulfate. Environ. Sci. Technol. 23, 1361—1368. 

Once they have reached higher pH, reducing conditions of the intestinal tract (Davis et al, 1992), sulhdes should be more stable, and may actually precipitate if reduced sulfur is present. Other solids, such as hydroxides or hydroxy-sulfates of aluminum, and possibly iron, may also precipitate. The increased pH should also lead to the increased sorption onto particulates of various metals and metalloids such as lead and copper (Smith, 1999). However, in vitro tests (Ruby et al, 1993) indicate that the increased complexing with unprotonated organic acids and enzymes helps offset the pH-driven precipitation and sorption of the base metals that were dominantly chloride-complexed in the stomach fluids. Arsenic and other oxyanionic species are likely to be sorbed as the stomach acids are neutralized, but may be partially desorbed once higher pH values are reached in the intestine (Ruby et al, 1996). 

Green patina, whose decorative aspect is highly appreciated, contains mostly basic salts. Their exact composition depends on the atmospheric conditions. In urban atmospheres they are mostly composed of hydroxy-sulfates and in marine atmospheres of hydroxy-chlorides. The patina forms more rapidly in polluted atmospheres, but even so, one generally has to wait a few years for a green patina to appear. Environments with a high SO2 concentration can prevent entirely the formation of the green patina, because the surface pH of the metal remains too low for the precipitation of basic salts. 

Quinoline-5-sulfonic acid, 8-hydroxy-7-iodo-metal complexes absorptiometry, 1,549 Quinolinium salts in gravimetry, 1, 535 Quinolinol metal complexes color photography, 6,107 8-Quinolinol biological activity, 6, 771 gallium and indium complexes radiopharmacology, 6, 971 radionuclide complexes radiopharmacology, 6,994 8-Quinolyl sulfate hydrolysis metal catalysis, 6,465 Quinones... 

Symmetrical and unsymmetrical benzoins have been rapidly oxidized to benzils in high yields using solid reagent systems, copper(II) sulfate-alumina [105] or Oxone-wet alumina [105, 106] under the influence of microwaves (Scheme 6.32). Conventionally, the oxidative transformation of a-hydroxy ketones to 1,2-diketones is accomplished by reagents such as nitric acid, Fehling s solution, thallium(III) nitrate (TTN), ytterbium(III) nitrate, ammonium chlorochromate-alumina and dayfen. In addition to the extended reaction time, most of these processes suffer from drawbacks such as the use of corrosive acids and toxic metals that generate undesirable waste products. 

Diazotization of the aminosulfonic acid and subsequent coupling onto the sodium salt of 2-hydroxy-3-naphthoic acid initially affords the monoazo compound in the form of its soluble sodium salt. Subsequent reaction with chlorides or sulfates of alkaline earth metals or with a manganese salt, frequently in the presence of a dispersion agent, or rosin or its derivatives, at elevated temperature yields the insoluble BONA pigment lake. 

Thus, sulfate conjugation and acetylation may be involved in the metabolic activation of N-hydroxy aromatic amines, glutathione conjugation may be important in the nephrotoxicity of compounds, methylation in metal toxicity, glucuronidation in the carcinogenicity of p-naphthylamine and 3, 2 -dimethyl-4-aminobiphenyl. 

The most interesting feature of this method, reviewed by Stepanov,62 is the ease with which the halogen atom is replaced by a hydroxyl group during the metallization process. This was first observed as long ago as 1931 when Delfs63 obtained the copper complex of 2-(2-hydroxy-naphthyl-l-azo)phenol-4-sulfonic acid (47) by heating an aqueous solution of l-chloro-2-(2-hydroxynaphthyl-l-azo)benzene-4-sulfonic acid (48), copper sulfate, sodium hydroxide and ammonia at 80 °C for 1 hour. 

---