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在存在和不存在溶解有机碳的情况下,砷酸盐和亚砷酸盐在水铁矿上的吸附作用

Adsorption of arsenate and arsenite on ferrihydrite in the presence and absence of dissolved organic carbon.

作者信息

Grafe Markus, Eick Matthew J, Grossl Paul R, Saunders Amy M

机构信息

Dep of Plant and Soil Sciences, Univ of Delaware, Newark 19717, USA.

出版信息

J Environ Qual. 2002 Jul-Aug;31(4):1115-23. doi: 10.2134/jeq2002.1115.

Abstract

The adsorption of As(V) and As(III) on synthetic two-line ferrihydrite in the presence and absence of a peat humic acid (HAp), Suwannee River fulvic acid (FA), or citric acid (CA) was investigated. Previous work with goethite has demonstrated the ability of dissolved organic carbon (DOC) to decrease As(V) and As(III) adsorption. The results obtained demonstrate that As(V) adsorption on ferrihydrite was decreased only in the presence of CA. Arsenate decreased the adsorption of all organic acids except HAp. Both FA and CA reduced As(III) adsorption on ferrihydrite, while HAp had no effect. Fulvic and citric acid adsorption on ferrihydrite was decreased in the presence of As(III); however, FA and CA adsorption increased at lower pH, which was consistent with decreased As(III) adsorption. Peat humic acid did not decrease As(III) adsorption, and we believe that the adsorption process of HAp and As(III) and As(V) on ferrihydrite are independent of each other. Previously, we observed that As(V) adsorption on goethite decreased in the presence of HAp > FA > CA, while As(III) adsorption on goethite was decreased similarly to that on ferrihydrite in the presence of CA > FA approximately HAp, yet As(III) adsorption on ferrihydrite was greater than on goethite. The observed differences between this study and the earlier study on goethite are believed to be an intricate function of ferrihydrite's surface characteristics, which affect the mechanisms of adsorption and hence the affinity of organic acids such as HAp, FA, and CA for the ferrihydrite surface. As such, the adsorption of DOCs to ferrihydrite are assumed to be less favorable and to occur with a fewer number of ligands, resulting in lower surface coverage of weaker bond strength.

摘要

研究了在有和没有泥炭腐殖酸(HAp)、苏万尼河黄腐酸(FA)或柠檬酸(CA)存在的情况下,合成的二线水铁矿对五价砷(As(V))和三价砷(As(III))的吸附情况。先前对针铁矿的研究表明,溶解有机碳(DOC)能够降低As(V)和As(III)的吸附。所得结果表明,仅在CA存在时,水铁矿对As(V)的吸附才会降低。砷酸盐降低了除HAp之外所有有机酸的吸附。FA和CA均降低了水铁矿对As(III)的吸附,而HAp则没有影响。在As(III)存在的情况下,黄腐酸和柠檬酸在水铁矿上的吸附减少;然而,FA和CA的吸附在较低pH值时增加,这与As(III)吸附减少一致。泥炭腐殖酸没有降低As(III)的吸附,并且我们认为HAp与As(III)以及As(V)在水铁矿上的吸附过程相互独立。此前,我们观察到在HAp > FA > CA存在时,针铁矿对As(V)的吸附降低,而在CA > FA约等于HAp存在时,针铁矿对As(III)的吸附降低情况与水铁矿类似,但水铁矿对As(III)的吸附大于针铁矿。据信,本研究与早期针对针铁矿的研究之间观察到的差异是水铁矿表面特性的复杂函数,该特性影响吸附机制,进而影响HAp、FA和CA等有机酸对水铁矿表面的亲和力。因此,假定DOC对水铁矿的吸附不太有利,且发生吸附时配体数量较少,导致键强度较弱的表面覆盖率较低。

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