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作 者:戴友芝[1] 张良长[1] 田凯勋[1] 罗春香[1]
出 处:《环境化学》2009年第1期49-53,共5页Environmental Chemistry
基 金:国家自然科学基金资助项目(No.20477034);湖南省教育厅资助科研项目(No.06C823).
摘 要:研究了2,3,4,6-四氯酚(TeCP)在超声波/零价铁协同体系中的降解,结果表明,拟一级动力学能很好的拟合降解过程,协同体系中TeCP一级降解速率常数为0.0141min^(-1),为同等条件下零价铁体系降解速率常数的10.07倍,且大于两者之和,说明两者之间存在明显协同效应;零价铁(Fe^0)投加量、初始pH值、初始TeCP浓度(C_0)、超声功率和溶液离子强度等控制参数对TeCP降解速率的影响表明,其拟一级速率常数在Fe^0量为2g·l^(-1),初始pH值为6.0,离子强度0.8mol·l^(-1)Na_2SO_4以及超声功率350W时达最大值,并随着C_0的升高而降低.The degradation of aqueous 2,3,4,6-tetrachlorophenol (TeCP) by ultrasound combined with element iron ( US/Fe^0) was investigated, the pseudo-first-order rate constant, kUS/Fe^0, for TeCP degradation by US/Fe^0 was 0. 0141min^-1, which was 10. 07 times as large as kFe0, and greater than the sum of kUS and kFe0, these evidences suggested that synergistic effects between US and Fe^0 existed. The influences of Fe^0 dose ( [ Fe^0] ), solution initial pH, initial TeCP concentration, solution ionic strength and ultrasonic power, on the rate constant of TeCP degradation by US/Fe^0, were studied. The rate constant was found largest at [ Fe^0] 2 g·l^-1 , initial pH 6.0, 0. 8mol·l^-1 Na2SO4 of ionic strength and 350 W of ultrasonic power respectively, and decrease with initial TeCP concentration increasing.
分 类 号:X132[环境科学与工程—环境科学]
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