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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 21 (1992), S. 525-532 
    ISSN: 1572-8927
    Keywords: Calcium ; molybdate ; aqueous ; thermodynamic ; complexation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The solubility of powellite [CaMoO4(c)] was studied in aqueous Na2MoO4, CaCl2 and Ca(NO3)2 solutions ranging in concentrations from 1×10−4M to 1.0M and over equilibration times extending to 36 days. Our experimental data were interpreted using the aqueous ion-interaction model of Pitzer and coworkers. The Ca2+−MoO 4 2− ion-interactions were found to be analogous to Ca2+−SO 4 2− . The use of Ca2+−MoO 4 2− ion-interactions parameters (β(0)=0.2, β(1) = 3.1973 and β(2)) and a logK sp of −7.93 gave excellent predictions of all of the experimental data. Commonion ternary interaction parameters such as MoO 4 2− −Cl− or MoO 4 2− −NO 3 − were not required.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 27 (1998), S. 435-454 
    ISSN: 1572-8927
    Keywords: EDTA ; HEDTA ; NTA ; IDA ; solubility ; strontium ; calcium ; waste processing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The effects of calcium, hydroxide, and carbonate on the displacement of Sr from four organic chelates: ethylenedinitrilotetraacetic acid (EDTA), N-(2-hydroxyethyl)ethylenedinitrilotriacetic acid (HEDTA) nitrilotriacetic acid (NTA), and iminidiacetic acid (IDA) was studied in solutions with high base and carbonate concentration. Comparison of solutions with and without added chelators allowed the speciation changes in solution to be directly determined. Increases in both carbonate and calcium concentration were effective in displacing Sr from the chelators even under high carbonate concentration. Increases in hydroxide were ineffective in removal of Sr from the chelators, even at base concentrations as high as 6M. Under certain specific conditions, most notably when both CaCO3(s) and SrCO3(s) are present in solution, chemical equilibrium constraints result in cancelation of activity coefficient changes for aqueous Sr and Ca organic chelate complexes. Under such conditions the predicted ratios of chelated Ca and Sr become independent of the ionic media and predictive relations using known equilibrium constants give very good representations of the experimental data. These results indicate that manipulation of metal ion displacement reactions during chemical processing of Sr–chelate solutions can result in the displacement of Sr from organic chelators. The implications of such strategies in processing high level waste supernatants stored at Department of Energy (DOE) sites is discussed.
    Type of Medium: Electronic Resource
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