Strontium hydroxide, complex with

H. 8-Hydroxyquinaldine (XI). The reactions of 8-hydroxyquinaldine are, in general, similar to 8-hydroxyquinoline described under (C) above, but unlike the latter it does not produce an insoluble complex with aluminium. In acetic acid-acetate solution precipitates are formed with bismuth, cadmium, copper, iron(II) and iron(III), chromium, manganese, nickel, silver, zinc, titanium (Ti02 + ), molybdate, tungstate, and vanadate. The same ions are precipitated in ammoniacal solution with the exception of molybdate, tungstate, and vanadate, but with the addition of lead, calcium, strontium, and magnesium aluminium is not precipitated, but tartrate must be added to prevent the separation of aluminium hydroxide. 

Coprecipitation of the metals is usually achieved from an aqueous solution of nitrates upon addition of anions such as carbonates, citrates, or oxalates (10)(24-27). First reports in this field have underlined the necessity to neutralize the pH of the solution in order to obtain complete precipitation of barium or strontium. Also, oxalate or citrate ligands may bind to two different cations. This should allow a better mixing at a microscopic level. However, care should be taken since some cations such as Y or La may precipitate as double salt complexes with alkaline ions that have been added to the solution as hydroxides in order to control the pH (24). 

Whereas all of the methods proposed for large-scale fractionation of starch that have been discussed depend directly on the ability of amylose to form itLsoluble complexes with polar organic compounds. Cantor and Wimmer s process is based on a totally different principle. If a molecularly disperse solution of starch contains a sufficient amount of calcium chloride and caustic alkali is added, a rapid and quantitative precipitation of the starch occurs, because of the formation of complexes (of calcium hydroxide with the starch polysaccharides) which are insoluble in an aqueous, saturated solution of calcium hydroxide. The same phenomenon is observed with the hydroxides of barium and strontium. 

OC-Hydroxycarboxylic Acid Complexes. Water-soluble titanium lactate complexes can be prepared by reactions of an aqueous solution of a titanium salt, such as TiCl, titanyl sulfate, or titanyl nitrate, with calcium, strontium, or barium lactate. The insoluble metal sulfate is filtered off and the filtrate neutralized using an alkaline metal hydroxide or carbonate, ammonium hydroxide, amine, or alkanolamine (78,79). Similar solutions of titanium lactate, malate, tartrate, and citrate can be produced by hydrolyzation of titanium salts, such as TiCl, in strongly (>pH 10) alkaline water isolation of the... 

The presence of normal concentrations of sodium, magnesium, and strontium have no net effect on the determination of calcium above the approximate level of accuracy of about 0.1% so that no correction factor seems necessary. A sufficient amount of titrant must be added to complex at least 98% of dissolved calcium before the buffer is added this apparently reduces the loss of calcium by coprecipitation with magnesium hydroxide. 

There are a number of interferences that can occur in atomic absorption and other flame spectroscopic methods. Anything that decreases the number of neutral atoms in the flame will decrease the absorption signal. Chemical interference is the most commonly encountered example of depression of the absorption signal. Here, the element of interest reacts with an anion in solution or with a gas in the flame to produce a stable compound in the flame. For example, calcium, in the presence of phosphate, will form the stable pyrophosphate molecule. Refractory elements will combine with 0 or OH radicals in the flame to produce stable monoxides and hydroxides. Fortunately, most of these chemical interferences can be avoided by adding an appropriate reagent or by using a hotter flame. The phosphate interferences, for example, can be eliminated by adding 1 % strontium chloride or lanthanum chloride to the solution. The strontium or lanthanum preferentially combines with the phosphate to prevent its reaction with the calcium. Or, EDTA can be added to complex the calcium and prevent its combination with the phosphate. 

Complexes of alkali metals and alkaline-earth metals with carbohydrates have been reviewed in this Series,134 and the interaction of alkaline-earth metals with maltose has been described.135 Standard procedures for the preparation of adducts of D-glucose and maltose with the hydroxides of barium, calcium, and strontium have been established. The medium most suitable for the preparation of the adduct was found to be 80% methanol. It is of interest that the composition of the adducts, from D-glucose, maltose, sucrose, and a,a-trehalose was the same, namely, 1 1, in all cases. The value of such complex-forming reactions in the recovery of metals from industrial wastes has been recognized. Metal hydroxide-sugar complexes may also play an important biological role in the transport of metal hydroxides across cell membranes. 

Yanagihara et al. [51 ] claimed that calcium was the only metal cation which catalyzed the epimerization they tried many others but only strontium had a weak effect. A closer investigation [52] showed cations that complex well with polyols [44] all catalyze the epimerization those metals tested by Yanagihara et al. were poor complex formers. Calcium hydroxide is best suited for this reaction because it has reasonable solubUity in water and is readily available. The reaction can also be conducted in methanol in which both calcium hydroxide and the sugars have only low solubility but when they are both present, the solvent dissolves many of them, owing to complex formation. 

Since alkoxides of low formal charge metals are highly condensed and therefore poorly reactive, the synthesis of many perovskites (ticanium. zirconium, niobium, barium, strontium or lead) can take place by hydrolysis of the alkoxide by an aqueous suspension of hydroxide (Ba, Sr) [121] or by an aqueous solution of a lead complex such as the acetate [122]. Iron is introduced as acetylacetonate in the case of PbFeo.jNbo.sOi [123]. The calcination temperature varies with the nature of the metallic cation. It must be adjusted if the formation of undesirable phases is possible, such as the pyrochlore phase in the case of PbMgo.33Nbo.66O3 and PbZri, (Ti 03 [122]. A fast ramp rate prevents or minimizes its formation. 

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