High arsenic groundwater in the Guide basin, northwestern China: Distribution and genesis mechanisms

2018 ◽  
Vol 640-641 ◽  
pp. 194-206 ◽  
Author(s):  
Zhen Wang ◽  
Huaming Guo ◽  
Wei Xiu ◽  
Jiao Wang ◽  
Mengmeng Shen
2020 ◽  
Author(s):  
Zhipeng Gao ◽  
◽  
Haicheng Weng ◽  
Huaming Guo

Water ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 338
Author(s):  
Chuanshun Zhi ◽  
Wengeng Cao ◽  
Zhen Wang ◽  
Zeyan Li

High–arsenic (As) groundwater poses a serious threat to human health. The upper and middle reaches of the Yellow River are well–known areas for the enrichment of high–arsenic groundwater. However, little is known about the distribution characteristics and formation mechanism of high-As groundwater in the lower reach of the Yellow River. There were 203 groundwater samples collected in different groundwater systems of the lower Yellow River for the exploration of its hydrogeochemical characteristics. Results showed that more than 20% of the samples have arsenic concentrations exceeding 10 μg/L. The high-As groundwater was mainly distributed in Late Pleistocene–Holocene aquifers, and the As concentrations in the paleochannels systems (C2 and C4) were significantly higher than that of the paleointerfluve system (C3) and modern Yellow River affected system (C5). The high-As groundwater is characterized by high Fe2+ and NH4+ and low Eh and NO3−, indicating that reductive dissolution of the As–bearing iron oxides is probably the main cause of As release. The arsenic concentrations strikingly showed an increasing tendency as the HCO3− proportion increases, suggesting that HCO3− competitive adsorption may facilitate As mobilization, too. In addition, a Gibbs diagram showed that the evaporation of groundwater could be another significant hydrogeochemical processes, except for the water–rock interaction in the study area. Different sources of aquifer medium and sedimentary structure may be the main reasons for the significant zonation of the As spatial distribution in the lower Yellow River.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Zhou Jiang ◽  
Ping Li ◽  
Yanhong Wang ◽  
Han Liu ◽  
Dazhun Wei ◽  
...  

Abstract Microbial metabolisms of arsenic, iron, sulfur, nitrogen and organic matter play important roles in arsenic mobilization in aquifer. In this study, microbial community composition and functional potentials in a high arsenic groundwater were investigated using integrated techniques of RNA- and DNA-based 16S rRNA gene sequencing, metagenomic sequencing and functional gene arrays. 16S rRNA gene sequencing showed the sample was dominated by members of Proteobacteria (62.3–75.2%), such as genera of Simplicispira (5.7–6.7%), Pseudomonas (3.3–5.7%), Ferribacterium (1.6–4.4%), Solimonas (1.8–3.2%), Geobacter (0.8–2.2%) and Sediminibacterium (0.6–2.4%). Functional potential analyses indicated that organics degradation, assimilatory sulfate reduction, As-resistant pathway, iron reduction, ammonification, nitrogen fixation, denitrification and dissimilatory nitrate reduction to ammonia were prevalent. The composition and function of microbial community and reconstructed genome bins suggest that high level of arsenite in the groundwater may be attributed to arsenate release from iron oxides reductive dissolution by the iron-reducing bacteria, and subsequent arsenate reduction by ammonia-producing bacteria featuring ars operon. This study highlights the relationship between biogeochemical cycling of arsenic and nitrogen in groundwater, which potentially occur in other aquifers with high levels of ammonia and arsenic.


Water ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 1126 ◽  
Author(s):  
Yanyan Qin ◽  
Yanping Cui ◽  
Lidan Lei ◽  
Ya Gao ◽  
Zhengwei Zhou ◽  
...  

A relatively low voltage can be favor of e- transfer and peroxide generation from dominant 2e--reduction of O2 on carbon materials as cathode, with low energy loss. In this study the conversion of As(III) in simulated high arsenic groundwater at low voltage was compared in a mixed and a anode–cathode separated electrolytic system. With applied voltages (the potential difference between cathode and anode) from 0.1 V to 0.8 V, As(III) was found to be efficiently converted to As(V) in the mixed electrolytic cells and in separated anodic cells. The complete oxidation of As(III) to As(V) at 0.1–0.8 V was also achieved on graphite in divided cathodic cells which could be long-running. The As(III) conversion process in mixed electrolytic cells, anodic cells and cathodic cells all conformed to the pseudo first-order kinetics equation. The energy consumed by As(III) conversion was decreased as the applied voltage declined. Low voltage electrolysis is of great significance for saving energy consumption and improving the current efficiency and can be applied to in-situ electrochemical pre-oxidation for As(III) in high arsenic groundwater.


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