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首页> 外文期刊>Journal of environmental sciences >Characterization of changes in extracellular polymeric substances and heavy metal speciation of waste activated sludge during typical oxidation solubilization processes
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Characterization of changes in extracellular polymeric substances and heavy metal speciation of waste activated sludge during typical oxidation solubilization processes

机译:典型氧化溶解过程中外细胞聚合物物质和废物活性污泥重金属形态的变化的表征

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Biopolymer solubilization is considered to be the rate-limiting stage of anaerobic digestion of waste activated sludge (WAS). Oxidation processes have been proven to be effective in disrupting sludge flocs and causing solubilization of the solid biopolymers. In this study, WAS was treated by NaNO2 or H2O2 oxidation at pH of 2. The changes in extracellular polymeric substances properties and the speciation of heavy metals were investigated. The results revealed that both NaNO2 and H2O2 treatments were effective in solubilizing organics in WAS, while the conversion of biopolymers in the two treatment processes was different. Free nitrous acid destroyed the gel network structure of EPS, and organic materials were released from the solid phase to the supernatant. Indigenous peroxidase catalyzed H2O2 to produce hydroxyl radicals which caused significant solubilization of biopolymers, and the protein-like substances were further degraded into micro-molecule polypeptides or amino acids at high dosages of H2O2. During the oxidation processes, Zn, Cd and Cu, with excellent mobility, tended to migrate to the supernatant, and thus were easy to remove through the liquid-solid separation process. Ni and As showed moderate migration ability, of which the residual fraction tended to transform into reducible and soluble fractions. With poor mobility, Cr and Pb mainly existed in the forms of residual and oxidizable fractions, which were difficult to dissolve and remove from WAS. Both NaNO2 and H2O2 treatment resulted in the enhancement of sludge solubilization efficiency and heavy metal mobility in WAS, but different heavy metals showed distinct migration and transformation behaviors. (C) 2018 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.
机译:生物聚合物溶解被认为是废物活性污泥的厌氧消化的速率限制阶段(是)。已被证明氧化过程可有效地破坏污泥絮凝物并引起固体生物聚合物的溶解。在该研究中,在pH的pH下被纳米2或H 2 O 2氧化治疗。研究了细胞外聚合物性质的变化和重金属的形状。结果表明,纳米2和H 2 O 2治疗在溶解有机物中是有效的,而两种处理过程中的生物聚合物的转化是不同的。游离亚硝酸破坏了EPS的凝胶网络结构,有机材料从固相释放到上清液中。本土过氧化物酶催化的H 2 O 2产生羟基自由基,其引起了生物聚合物的显着溶解,并且蛋白质物质进一步降解到高剂量H 2 O 2的微量分子多肽或氨基酸中。在氧化过程中,Zn,Cd和Cu具有优异的迁移率,倾向于迁移到上清液中,因此易于除去通过液体固体分离过程。 Ni和表现出中度迁移能力,其中残余部分倾向于转化为可降解和可溶性的级分。迁移率差,Cr和Pb主要存在于残留和可氧化的级分的形式中,这难以溶解和除去。纳米2和H 2 O 2处理都导致污泥溶解效率和重金属迁移率的增强,但不同的重金属显示出明显的迁移和转化行为。 (c)2018中国科学院生态环境科学研究中心。 elsevier b.v出版。

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