Patel Khageshwar Singh, Pandey Piyush Kant, Martín-Ramos Pablo, Corns Warren T, Varol Simge, Bhattacharya Prosun, Zhu Yanbei
Department of Applied Sciences, Amity University Manth (Kharora), State Highway 9 Raipur-493225 CG India
Amity University Manth (Kharora), State Highway 9 Raipur-493225 CG India
RSC Adv. 2023 Mar 17;13(13):8803-8821. doi: 10.1039/d3ra00789h. eCollection 2023 Mar 14.
Arsenic is one of the regulated hazard materials in the environment and a persistent pollutant creating environmental, agricultural and health issues and posing a serious risk to humans. In the present review, sources and mobility of As in various compartments of the environment (air, water, soil and sediment) around the World are comprehensively investigated, along with measures of health hazards. Multiple atomic spectrometric approaches have been applied for total and speciation analysis of As chemical species. The LoD values are basically under 1 μg L, which is sufficient for the analysis of As or its chemical species in environmental samples. Both natural and anthropogenic sources contributed to As in air, while fine particulate matter tends to have higher concentrations of arsenic and results in high concentrations of As up to a maximum of 1660 ng m in urban areas. Sources for As in natural waters (as dissolved or in particulate form) can be attributed to natural deposits, agricultural and industrial effluents, for which the maximum concentration of 2000 μg L was found in groundwater. Sources for As in soil can be the initial contents, fossil fuel burning products, industrial effluents, pesticides, and so on, with a maximum reported concentration up to 4600 mg kg. Sources for As in sediments can be attributed to their reservoirs, with a maximum reported concentration up to 2500 mg kg. It is notable that some reported concentrations of As in the environment are several times higher than permissible limits. However, many aspects of arsenic environmental chemistry including contamination of the environment, quantification, mobility, removal and health hazards are still unclear.
砷是环境中受管制的有害物质之一,是一种持久性污染物,会引发环境、农业和健康问题,并对人类构成严重风险。在本综述中,全面研究了全球环境各部分(空气、水、土壤和沉积物)中砷的来源和迁移性,以及健康危害的衡量指标。多种原子光谱方法已应用于砷化学物种的总量和形态分析。检测限基本低于1 μg/L,这足以用于分析环境样品中的砷或其化学物种。空气当中的砷有自然源和人为源,而细颗粒物中的砷浓度往往较高,导致城市地区砷的浓度高达1660 ng/m³。天然水体中砷的来源(以溶解态或颗粒态形式存在)可归因于天然沉积物、农业和工业废水,其中地下水中砷的最大浓度为2000 μg/L。土壤中砷的来源可以是初始含量、化石燃料燃烧产物、工业废水、农药等,报告的最大浓度高达4600 mg/kg。沉积物中砷的来源可归因于其储存库,报告的最大浓度高达2500 mg/kg。值得注意的是,环境中一些报告的砷浓度比允许限值高出几倍。然而,砷环境化学的许多方面,包括环境污染、量化、迁移性、去除和健康危害,仍然不清楚。