Groundwater arsenic pollution has received much attention worldwide for decades as a serious threat to public health, but the mechanisms responsible for arsenic mobilization are not fully understood. Groundwater and bore drilling sediment samples from Qiji county, a small geographical agricultural area with endemic arsenicosis, are collected for demonstrating the occurrence and speciation of arsenic in groundwater and sediments, and arsenic release between solid-liquid phase influenced by human activities. Results show that arsenic concentrations in groundwater vary from 5 μg/L to 19.6 μg/L, with 80% exceeding the maximum permissible limits required by WHO (10 μg/L) for drinking water and therefore constituting a health risk for humans. In a weak oxidizing environment (oxidation-reduction potential (ORP): 12.9 mV-151 mV), inorganic As(V) accounts for 85% of total dissolved As, which to some extent alleviates the harm of As pollution on humans. Total As content in the sediments is in the range of 6.98 mg/kg and 14.34 mg/kg (median of 10.71 mg/kg), three times higher than the average value of many countries. Sequential chemical leaching indicates that 11% of arsenic in sediments is labile bound and may be closely related to the arsenic in groundwater. Additionally, irrigation intensity contributes to arsenic release with diverse As3+/As5+ by dissolving weakly bound arsenic rapidly. Subsequently part of As(III) is oxidized to As(V). Competitive and/or alkaline desorption of As(V), which had been adsorbed by FeMn (hydrous)-oxides and carbonates in the unsaturated zone and the aquifer, exerts a significant role in releasing arsenic into the groundwater. Our study indicates that systematic management and regulation of irrigation intensity are required to prevent further deterioration of groundwater resources.
Keywords: Adsorption-desorption; Arsenic release; Irrigated areas; Oxidation; Sequential extraction; Species of arsenic.
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