Fe(II) bio-oxidation mediates red mud transformations to form Fe(III)/Al (hydr)oxide adsorbent for efficient As(V) removal under acidic conditions
Zhang, Duo-Rui1; Chen, Hong-Rui1; Zhao, Xiao-Juan2; Xia, Jin-Lan1; Nie, Zhen-yuan1; Zhang, Rui-yong3,4; Shu, Wen-Sheng5; Pakostova, Eva6
2022-07-01
发表期刊CHEMICAL ENGINEERING JOURNAL
ISSN1385-8947
卷号439页码:14
通讯作者Xia, Jin-Lan([email protected])
摘要Acidic wastewater rich in arsenic (As) is one of the most hazardous types of liquid waste and has caused severe environmental pollution over the past few decades due to a lack of cost-effective and environment-friendly disposal technologies. Here, a new strategy for the efficient immobilization of As(V) under acidic conditions is presented. The approach uses Fe(II) bio-oxidation by the acidophilic bacterium Sulfobacillus (Sb.) thermosulfidooxidans to transform red mud into a low-cost Fe(III)/Al (hydr)oxide adsorbent for As(V) removal. The mechanisms of the formation of the adsorbent and subsequent adsorption of As onto its surface were investigated, together with the relationship between the adsorbent structure and As adsorption efficiency. The [Fe (II)]ini greatly affected the growth of Sb. thermosulfidooxidans, Fe/Al speciation, and surface structure of the adsorbent, as well as the As removal capacity. The aluminosilicates in RM provided numerous sites for Fe(III) adsorption, inhibiting the transformation of amorphous Fe(III) (hydr)oxides to crystalline Fe(III) minerals. The newly formed Fe(OH)(3) and schwertmannite played a dominant role in As(V) immobilization. The transformation of the amorphous Fe(III) (hydr)oxides to more crystalline Fe(III) minerals, caused by an excess of Fe(II) (2 <= [Fe (II)]ini <= 4 g/L), resulted in a significant decrease in the As adsorption capacity (reduce ratio: 29.3-53.5%). The Fe(III)/Al (hydr)oxide adsorbent bio-synthesized under [Fe(II)]ini of 1 g/L showed the highest As(V) adsorption efficiency (89.9 mg/g; at pH 2.0), which was significantly higher than that of the original RM under the same conditions (5.7 mg/g). The adsorption process followed the pseudo-second-order kinetic and Langmuir isotherm models.
关键词Arsenic removal Iron oxidation Red mud Fe(III) Al (hydr)oxides Iron speciation transformation
DOI10.1016/j.cej.2022.135753
收录类别SCI
语种英语
资助项目National Natural Science of China[51861135305]; National Natural Science of China[41830318]; Open Funds of Beijing Synchrotron Radiation Facility[2019-BEPC-PT-003348]
WOS研究方向Engineering
WOS类目Engineering, Environmental ; Engineering, Chemical
WOS记录号WOS:000783179900001
出版者ELSEVIER SCIENCE SA
引用统计
被引频次:20[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/178973
专题海洋环境腐蚀与生物污损重点实验室
通讯作者Xia, Jin-Lan
作者单位1.Cent South Univ, Sch Minerals Proc & Bioengn, Key Lab Biomet, Minist Educ China, Changsha 410083, Peoples R China
2.Chinese Acad Sci, Beijing Synchrotron Radiat Facil, Inst High Energy Phys, Beijing 100049, Peoples R China
3.Chinese Acad Sci, Inst Oceanol, Key Lab Marine Environm Corros & Biofouling, Qingdao 266071, Peoples R China
4.Pilot Natl Lab Marine Sci & Technol Qingdao, Open Studio Marine Corros & Protect, Qingdao 266237, Peoples R China
5.South China Normal Univ, Sch Life Sci, Guangzhou 510631, Peoples R China
6.Coventry Univ, Ctr Sport Exercise & Life Sci, Coventry CV1 5FB, W Midlands, England
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Zhang, Duo-Rui,Chen, Hong-Rui,Zhao, Xiao-Juan,et al. Fe(II) bio-oxidation mediates red mud transformations to form Fe(III)/Al (hydr)oxide adsorbent for efficient As(V) removal under acidic conditions[J]. CHEMICAL ENGINEERING JOURNAL,2022,439:14.
APA Zhang, Duo-Rui.,Chen, Hong-Rui.,Zhao, Xiao-Juan.,Xia, Jin-Lan.,Nie, Zhen-yuan.,...&Pakostova, Eva.(2022).Fe(II) bio-oxidation mediates red mud transformations to form Fe(III)/Al (hydr)oxide adsorbent for efficient As(V) removal under acidic conditions.CHEMICAL ENGINEERING JOURNAL,439,14.
MLA Zhang, Duo-Rui,et al."Fe(II) bio-oxidation mediates red mud transformations to form Fe(III)/Al (hydr)oxide adsorbent for efficient As(V) removal under acidic conditions".CHEMICAL ENGINEERING JOURNAL 439(2022):14.
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