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A method for the speciation of aluminum in natural surface waters.

机译:一种在天然地表水中对铝进行形态分析的方法。

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摘要

As a result of a water chemistry survey at Whetstone Brook in western Massachusetts, during an acid mitigation study using a limestone doser, unusually high levels of aluminum were found in sediment pore waters with an overlying layer of limestone. Because of potential fish and biotic toxicity and the problems associated with commonly used speciation techniques for aluminum, a more comprehensive scheme was proposed including aluminum determination by optimized methods of GFAAS, cation exchange on a strong acid resin, and ultrafiltration at 0.5 kd, 1 kd, 3 kd and 10 kd MW cut-offs. The method of chemical extraction into MIBK following chelation by 8-HQ was also evaluated and all the experimental results were compared to a theoretical speciation using equilibrium calculations.;No experimental conditions were found that could extract a consistent fraction with all the model organic ligands for the 8-HQ extraction procedure. Recoveries ranged from 10% to 200% of the organically bound aluminum relative to inorganic standards. Cation-exchangeable aluminum, complexed with malonate, oxalate, phthalate and salicylate, matched a theoretical speciation to within 5%. Theoretical and experimental results for citrate complexed aluminum differed by 24%.;Ultrafiltrate experiments indicated that size fractionation may add more information about the aggregation of aluminum-organic monomers into higher MW oligomers and polymers. In all the synthetic systems studied there appears to be aggregation at lower MW values and the citrate, phthalate and salicylate complexes have fractions greater than 10 kd.;Experiments with fulvic acid showed that approximately 80% of the aluminum complexed species were noncationic. Greater than 90% of the aluminum-fulvate was recovered in the MW range above 10 kd.;Comparisons with stability constants in the literature showed that none of the available constants could predict the behavior of the citrate system and although constants were found that could predict the fulvate system, the majority could not.
机译:在马萨诸塞州西部的Whetstone Brook进行的水化学调查结果显示,在使用石灰石计量器进行酸减缓研究期间,在沉积物孔隙水中发现了高含量的铝,上面有一层石灰石。由于潜在的鱼类和生物毒性以及与常用的铝形态学技术相关的问题,提出了一种更全面的方案,包括通过优化的GFAAS方法测定铝,在强酸树脂上进行阳离子交换以及在0.5 kd,1 kd下进行超滤,3 kd和10 kd MW临界值。还评价了8-HQ螯合后化学提取MIBK的方法,并用平衡计算将所有实验结果与理论形态进行了比较;没有发现实验条件可以提取与所有模型有机配体一致的馏分。 8-HQ提取程序。相对于无机标准品,回收率范围为有机结合铝的10%至200%。与丙二酸酯,草酸酯,邻苯二甲酸酯和水杨酸酯络合的可阳离子交换的铝,与理论形态相符的比例在5%以内。柠檬酸盐络合铝的理论和实验结果相差24%。超滤液实验表明,分级分离可能会提供更多有关铝有机单体聚集为更高MW低聚物和聚合物的信息。在所有研究的合成系统中,似乎都在较低的MW值下发生聚集,并且柠檬酸盐,邻苯二甲酸盐和水杨酸盐复合物的分数大于10 kd。在高于10 kd的MW范围内回收了超过90%的富铝铝酸盐;与文献中的稳定常数比较表明,没有可用的常数可以预测柠檬酸盐系统的行为,尽管发现了可以预测的常数fulvate系统,大多数不能。

著录项

  • 作者

    Kerr, Peter Allan.;

  • 作者单位

    University of Massachusetts Amherst.;

  • 授予单位 University of Massachusetts Amherst.;
  • 学科 Inorganic chemistry.;Toxicology.;Environmental science.;Limnology.
  • 学位 Ph.D.
  • 年度 1997
  • 页码 149 p.
  • 总页数 149
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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