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异化铁(III)还原与砷(V)还原对砷保留和迁移的对比效应

Contrasting effects of dissimilatory iron (III) and arsenic (V) reduction on arsenic retention and transport.

作者信息

Kocar Benjamin D, Herbel Mitchell J, Tufano Katherine J, Fendorf Scott

机构信息

Department of Geological and Environmental Sciences, Stanford University, Stanford, California 94305, USA.

出版信息

Environ Sci Technol. 2006 Nov 1;40(21):6715-21. doi: 10.1021/es061540k.

Abstract

Reduction of arsenate As(V) and As-bearing Fe (hydr)- oxides have been proposed as dominant pathways of As release within soils and aquifers. Here we examine As elution from columns loaded with ferrihydrite-coated sand presorbed with As(V) or As(III) at circumneutral pH upon Fe and/or As reduction; biotic stimulated reduction is then compared to abiotic elution. Columns were inoculated with Shewanella putrefaciens strain CN-32 or Sulfurospirillum barnesii strain SES-3, organisms capable of As (V) and Fe (III) reduction, or Bacillus benzoevorans strain HT-1, an organism capable of As(V) but not Fe(III) reduction. On the basis of equal surface coverages, As(III) elution from abiotic columns exceeded As(V) elution by a factor of 2; thus, As(III) is more readily released from ferrihydrite under the imposed reaction conditions. Biologically mediated Asreduction induced by B. benzoevorans enhances the release of total As relative to As (V) under abiotic conditions. However, under Fe reducing conditions invoked by either S. barnesii or S. putrefaciens, approximately three times more As (V or III) was retained within column solids relative to the abiotic experiments, despite appreciable decreases in surface area due to biotransformation of solid phases. Enhanced As sequestration upon ferrihydrite reduction is consistent with adsorption or incorporation of As into biotransformed solids. Our observations indicate that As retention and release from Fe (hydr)oxide(s) is controlled by complex pathways of Fe biotransformation and that reductive dissolution of As-bearing ferrihydrite can promote As sequestration rather than desorption under conditions examined here.

摘要

砷酸盐As(V)和含砷铁(氢)氧化物的还原被认为是土壤和含水层中砷释放的主要途径。在此,我们研究了在中性pH条件下,负载有预吸附As(V)或As(III)的水铁矿包覆砂柱在铁和/或砷还原时的砷洗脱情况;然后将生物刺激还原与非生物洗脱进行比较。柱中接种了腐败希瓦氏菌菌株CN-32或巴恩斯硫螺旋菌菌株SES-3,这两种微生物能够还原As(V)和Fe(III),或者接种了苯甲酸芽孢杆菌菌株HT-1,该微生物能够还原As(V)但不能还原Fe(III)。在相同表面覆盖率的基础上,非生物柱中As(III)的洗脱量比As(V)的洗脱量高出2倍;因此,在设定的反应条件下,As(III)更容易从水铁矿中释放出来。在非生物条件下,苯甲酸芽孢杆菌诱导的生物介导的砷还原相对于As(V)增强了总砷的释放。然而,在巴恩斯硫螺旋菌或腐败希瓦氏菌引发的铁还原条件下,尽管由于固相生物转化导致表面积明显减小,但相对于非生物实验,柱固体中保留的As(V或III)大约多了三倍。水铁矿还原时砷的螯合增强与砷吸附或掺入生物转化固体中一致。我们的观察结果表明,砷在铁(氢)氧化物中的保留和释放受铁生物转化的复杂途径控制,并且在此研究的条件下,含砷水铁矿的还原溶解可促进砷的螯合而非解吸。

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