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Arsenate Remediation Using Nanosized Modified Zerovalent Iron Particles

机译:纳米改性零价铁颗粒对砷的修复

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Arsenate [As (V)J removal kinetics in aqueous solutions using modified nanosized zerovalent iron (Fe~0) particles such as NiFe and PdFe was studied. NiFe and PdFe particles were synthesized by the borohydride reduction of nickel and palladium salts on Fe~0 particles. Pseudo-first-order rate equations were found to satisfactorily describe arsenate removal kinetics using Fe~0, NiFe, and PdFe particles (solids concentration of 2 g L~(-1)) at low arsenate concentrations (1.35 mM). As compared to zerovalent iron (k_(obs) of 0.037 min~(-1)), the arsenate removal rate was up to 2.5 times faster (k_(obs) of 0.091 min~(-1)) using NiFe particles, whereas it was threefold lower in the case of PdFe particles (k_(obs) of 0.011 min~(-1)). With increasing contact times, deviation from first-order kinetics was observed, presumably arising from the loss of available sites on the solid surface. The surface area normalized pseudo-first-order rate constant k_(sa) was 0.0089 L m~(-2) min~(-1) for NiFe. Additional experiments were performed to study the influence of initial arsenate concentration (0.67 and 338 mM), temperature (25, 45, and 65℃) and competing inorganic anions (sulfate, chloride, nitrate, phosphate, and chromate) on arsenate removal using NiFe particles. Increasing temperatures (25-65℃) increased arsenate removal rates, whereas competing sorption of phosphate and sulfate inhibited arsenate removal.
机译:研究了使用改性的纳米零价铁(Fe〜0)颗粒如NiFe和PdFe去除水溶液中砷[As(V)J的动力学。 NiFe和PdFe颗粒是通过硼氢化物还原Fe〜0颗粒上的镍和钯盐而合成的。发现伪一阶速率方程可以令人满意地描述在低砷酸盐浓度(1.35 mM)下使用Fe〜0,NiFe和PdFe颗粒(固体浓度为2 g L〜(-1))去除砷的动力学。与零价铁(k_(obs)为0.037 min〜(-1))相比,使用NiFe颗粒时砷的去除速度快了2.5倍(k_(obs)为0.091 min〜(-1)),而在PdFe颗粒的情况下(k_(obs)为0.011 min〜(-1))降低了三倍。随着接触时间的增加,观察到与一级动力学的偏离,可能是由于固体表面可用位点的损失所致。 NiFe的表面积归一化拟一阶速率常数k_(sa)为0.0089 L m〜(-2)min〜(-1)。进行了其他实验,研究了初始砷酸盐浓度(0.67和338 mM),温度(25、45和65℃)和竞争性无机阴离子(硫酸根,氯离子,硝酸根,磷酸根和铬酸根)对使用NiFe去除砷的影响。粒子。温度升高(25-65℃)会提高砷的去除率,而磷酸盐和硫酸盐的竞争性吸附会抑制砷的去除。

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