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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Talanta 40 (1993), S. 147-155 
    ISSN: 0039-9140
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Soil Science Society of America journal 62 (1998), S. 602-610 
    ISSN: 1435-0661
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: -1 ). One of the soils (the Benge series A horizon) was adjusted to pHs from to 8.3, and extracted with methanol-modified supercritical CO2. Recoveries from this soil increased from 41 to 76% with decreasing pH. For soils at natural pHs, when a weak acid modifier (benzoic acid) was used in addition to methanol, the 2,4-D recovery ranged from 21 to 86%, increasing with decreasing organic C concentration. Treating the samples to the lowest pHs practical (1.2-1.6) with HCl and extracting with methanol-modified supercritical CO2 was more successful than utilizing the weak acid-methanol modifier, except for the soil with very low organic C. Recoveries after HCl treatment ranged from 80 to 94%. Two soils from 2,4-D-treated fields yielded more 2,4-D by modified SFE at pH 1.2 than by a modified version of the method recommended by the U.S. Environmental Protection Agency. The results suggest that organic acids like 2,4-D can be successfully extracted at low pH, even from soils high in organic C. Low recoveries from soils high in organic C appear to result from proton consumption by natural soil organic matter during extraction.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Soil Science Society of America journal 62 (1998), S. 1530-1537 
    ISSN: 1435-0661
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Mining activities and arsenical pesticide applications can introduce arsenate compounds into soils and sediments. Under water-saturated (flooded) soil conditions, arsenate solids are subjected to biotically generated reducing conditions and may undergo reductive dissolution. While thermodynamic calculations have been used to predict the conditions under which mineral-associated As undergoes reduction, there is relatively little data from systems in which well-characterized arsenate solids have been subjected to reducing conditions, and a limited amount of information about the reduction of mineral-bound arsenate. In this study, the behavior of five arsenates was observed under reducing conditions generated by flooded soils. The apparent solubility of the arsenates decreased in the order CaHAsO4 = Na2HasO4\cdot2H2O 〉 AlAsO4\cdot2H2O 〉 MnHAsO4 〉 FeAsO4\cdot2H2O under oxic conditions; under anoxic conditions (redox potential 〈0 m V) the apparent solubility was FeAsO4\cdot2H2O ≥CaHAsO4 = Na2HasO4\cdot7H2O 〉 AlAsO4\cdot2H2O 〉 MnHAsO4. Calcium and sodium arsenates completely dissolved under the initial oxidizing conditions. X-ray absorption near-edge structure (XANES) spectroscopy indicated that As in AlAsO4\cdot2H2O rapidly transformed to solid-phase As(III). Manganese arsenate yielded the least solution and solid-phase As(III) of all of the minerals. Iron arsenate underwent reductive dissolution, releasing As(III) to solution and solid phases, and thus may yield solution or solid-phase As(III) if prolonged anoxic conditions prevail.
    Type of Medium: Electronic Resource
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