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采用连续提取法结合酸挥发性硫化物分析,对细菌硫酸盐还原生物反应器中固相材料的重金属形态进行分析。

Heavy metal speciation in solid-phase materials from a bacterial sulfate reducing bioreactor using sequential extraction procedure combined with acid volatile sulfide analysis.

作者信息

Jong Tony, Parry David L

机构信息

Environmental Analytical Chemistry Unit, School of Science, Faculty of Education, Health & Science, Charles Darwin University, Darwin, 0909, Australia.

出版信息

J Environ Monit. 2004 Apr;6(4):278-85. doi: 10.1039/b316586h. Epub 2004 Mar 17.

Abstract

Heavy metal mobility, bioavailability and toxicity depends largely on the chemical form of metals and ultimately determines potential for environmental pollution. For this reason, determining the chemical form of heavy metals and metalloids, immobilized in sludges by biological mediated sulfate reduction, is important to evaluate their mobility and bioavailability. A modified Tessier sequential extraction procedure (SEP), complemented with acid volatile sulfide (AVS) and simultaneous extracted metals (SEM) measurements, were applied to determine the partitioning of five heavy metals (defined as Fe, Ni, Zn and Cu, and the metalloid As) in anoxic solid-phase material (ASM) from an anaerobic, sulfate reducing bioreactor into six operationally defined fractions. These fractions were water soluble, exchangeable, bound to carbonates (acid soluble), bound to Fe-Mn oxides (reducible), bound to organic matter and sulfides (oxidizable) and residual. It was found that the distribution of Fe, Ni, Zn, Cu and As in ASM was strongly influenced by its association with the above solid fractions. The fraction corresponding to organic matter and sulfides appeared to be the most important scavenging phases of As, Fe, Ni, Zn and Cu in ASM (59.8-86.7%). This result was supported by AVS and SEM (Sigma Zn, Ni and Cu) measurements, which indicated that the heavy metals existed overwhelmingly as sulfides in the organic matter and sulfide fraction. A substantial amount of Fe and Ni at 16.4 and 20.1%, respectively, were also present in the carbonate fraction, while an appreciable portion of As (18.3%) and Zn (19.4%) was bound to Fe-Mn oxides. A significant amount of heavy metals was also associated with the residual fraction, ranging from 2.1% for Zn to 18.8% for As. Based on the average total extractable heavy metal (TEHM) values, the concentration of heavy metals in the ASM was in the order of Cu > Ni > Zn > Fe > As. If the mobility and bioavailability of heavy metals are assumed to be related to their solubility and chemical forms, and that they decrease with each successive extraction step, then the apparent mobility and bioavailability of these five heavy metals in ASM increase in the order of Cu < As < Ni < Fe < Zn. The SEM/AVS ratio was less than one in eight replicate ASM samples, indicating that the ASM was non-toxic with regards to having a low probability of bioavailable metals in the pore water.

摘要

重金属的迁移性、生物可利用性和毒性在很大程度上取决于金属的化学形态,并最终决定环境污染的可能性。因此,确定通过生物介导的硫酸盐还原作用固定在污泥中的重金属和类金属的化学形态,对于评估它们的迁移性和生物可利用性很重要。采用一种改进的 Tessier 连续提取程序(SEP),并辅以酸挥发性硫化物(AVS)和同步提取金属(SEM)测量,来确定来自厌氧硫酸盐还原生物反应器的缺氧固相材料(ASM)中五种重金属(定义为 Fe、Ni、Zn 和 Cu,以及类金属 As)在六个操作定义的组分中的分配情况。这些组分分别是水溶性的、可交换的、与碳酸盐结合的(酸溶性的)、与铁锰氧化物结合的(可还原的)、与有机物和硫化物结合的(可氧化的)以及残留的。研究发现,ASM 中 Fe、Ni、Zn、Cu 和 As 的分布受其与上述固体组分的结合情况的强烈影响。对应于有机物和硫化物的组分似乎是 ASM 中 As、Fe、Ni、Zn 和 Cu 最重要的清除相(59.8 - 86.7%)。AVS 和 SEM(总 Zn、Ni 和 Cu)测量结果支持了这一结果,表明重金属在有机物和硫化物组分中绝大多数以硫化物形式存在。分别有 16.4%和 20.1%的大量 Fe 和 Ni 也存在于碳酸盐组分中,而相当一部分的 As(18.3%)和 Zn(19.4%)与铁锰氧化物结合。大量重金属也与残留组分相关,范围从 Zn 的 2.1%到 As 的 18.8%。基于平均总可提取重金属(TEHM)值,ASM 中重金属的浓度顺序为 Cu > Ni > Zn > Fe > As。如果假设重金属的迁移性和生物可利用性与其溶解度和化学形态有关,并且随着每个连续提取步骤而降低,那么这五种重金属在 ASM 中的表观迁移性和生物可利用性按 Cu < As < Ni < Fe < Zn 的顺序增加。在八个重复的 ASM 样品中,SEM/AVS 比值小于 1,表明 ASM 对于孔隙水中生物可利用金属的可能性较低而言是无毒的。

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