Department of Marine Science, Texas A&M University, Galveston, TX 77551, USA.
Anal Chim Acta. 2011 Dec 5;708(1-2):52-60. doi: 10.1016/j.aca.2011.08.017. Epub 2011 Aug 12.
Chemically selective chemisorbents are needed to monitor natural and engineered waters for anthropogenic releases of stable and radioactive contaminants. Here, a number of individual and mixtures of chemisorbents were investigated for their ability to extract select fission and activation product elements from marine and coastal waters, including Co, Zr, Ru, Ag, Te, Sb, Ba, Cs, Ce, Eu, Pa, Np, and Th. Conventional manganese oxide and cyanoferrate sorbents, including commercially available Anfezh and potassium hexacyanocobalt(II) ferrate(II) (KCFC), were tested along with novel nano-structured surfaces (known as Self Assembled Monolayers on Mesoporous Supports or SAMMS) functionalized with a variety of moieties including thiol, diphosphonic acid (DiPhos-), methyl-3,4 hydroxypyridinone (HOPO-), and cyanoferrate. Extraction efficiencies were measured as a function of salinity, organic content, temperature, flow rate and sample size for both synthetic and natural fresh and saline waters under a range of environmentally relevant conditions. The effect of flow rate on extraction efficiency, from 1 to 70 mL min(-1), provided some insight on rate limitations of mechanisms affecting sorption processes. Optimized mixtures of sorbent-ligand chemistries afforded excellent retention of all target elements, except, Ba and Sb. Mixtures of tested chemisorbents, including MnO(2)/Anfezh and MnO(2)/KCFC/Thiol (1-3 mm)-SAMMS, extracted 8 of the 11 target elements studied to better than 80% efficiency, while a mixture of MnO(2)/Anfezh/Thiol (75-150 μm)-SAMMS mixture was able to extract 7 of the 11 target elements to better than 90%. Results generated here indicate that flow rate should be less of a consideration for experimental design if sampling from fresh water containing variable amounts of DOM, rather than collecting samples from salt water environments. Relative to the capability of any single type of chemisorbent tested, optimized mixtures of several sorbents are able to increase the number of elements that can be efficiently and simultaneously extracted from natural waters.
需要使用化学选择性化学吸附剂来监测天然和人工水域中稳定和放射性污染物的人为释放。在这里,研究了一些单一和混合物的化学吸附剂,以评估它们从海洋和沿海水域中提取选择的裂变和活化产物元素的能力,包括 Co、Zr、Ru、Ag、Te、Sb、Ba、Cs、Ce、Eu、Pa、Np 和 Th。传统的氧化锰和氰亚铁酸盐吸附剂,包括市售的 Anfezh 和六氰合钴(II)铁(II)酸钾(KCFC),以及新型纳米结构表面(称为介孔载体上的自组装单分子层或 SAMMS),都与各种官能团(包括硫醇、二膦酸(DiPhos-)、3,4-甲基羟吡啶酮(HOPO-)和氰亚铁酸盐)进行了功能化,都进行了测试。在一系列环境相关条件下,测量了从合成和天然淡水和盐水样本中,作为盐度、有机含量、温度、流速和样本量的函数的萃取效率。流速对萃取效率的影响(从 1 到 70 mL min(-1))为影响吸附过程的机制的速率限制提供了一些见解。优化的吸附剂-配体化学混合物为所有目标元素提供了极好的保留,除了 Ba 和 Sb。测试的化学吸附剂混合物,包括 MnO(2)/Anfezh 和 MnO(2)/KCFC/硫醇(1-3 毫米)-SAMMS,以优于 80%的效率提取了研究的 11 个目标元素中的 8 个,而 MnO(2)/Anfezh/硫醇(75-150μm)-SAMMS 混合物则能够以优于 90%的效率提取 11 个目标元素中的 7 个。这里生成的结果表明,如果从含有可变量 DOM 的淡水而不是从盐水环境中采集样本,流速在实验设计中应该不那么重要。相对于测试的任何单一类型化学吸附剂的能力,几种吸附剂的优化混合物能够增加可以从天然水中高效且同时提取的元素数量。