Size-fractionation of groundwater arsenic in alluvial aquifers of West Bengal, India: The role of organic and inorganic colloids
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- 作者：Santanu Majumder ; Bibhash Nath ; Simita Sarkar ; Debashis Chatterjee ; Gabriela Roman-Ross ; Manuela Hidalgo
- 关键词：Size-fractionation ; Groundwater ; Arsenic ; Dissolved organic carbon (DOC) ; Organometallic colloids
- 刊名：Science of the Total Environment
- 出版年：15 January, 2014
- 年：2014
- 卷：468-469
- 期：Complete
- 页码：804-812
- 全文大小：1362 K
文摘
Dissolved organic carbon (DOC) and Fe mineral phases are known to influence the mobility of arsenic (As) in groundwater. Arsenic can be associated with colloidal particles containing organic matter and Fe. Currently, no data is available on the dissolved phase/colloidal association of As in groundwater of alluvial aquifers in West Bengal, India. This study investigated the fractional distribution of As (and other metals/metalloids) among the particulate, colloidal and dissolved phases in groundwater to decipher controlling behavior of organic and inorganic colloids on As mobility. The result shows that 83-94% of As remained in the 鈥榯ruly dissolved鈥?phases (i.e., < 0.05 渭m size). Strong positive correlation between Fe and As (r2 between 0.65 and 0.94) is mainly observed in the larger (i.e., > 0.05 渭m size) colloidal particles, which indicates the close association of As with larger Fe-rich inorganic colloids. In smaller (i.e., < 0.05 渭m size) colloidal particles strong positive correlation is observed between As and DOC (r2 = 0.85), which highlights the close association of As with smaller organic colloids. As(III) is mainly associated with larger inorganic colloids, whereas, As(V) is associated with smaller organic/organometallic colloids. Scanning Electron Microscopy and Energy Dispersive X-ray spectroscopy confirm the association of As with DOC and Fe mineral phases suggesting the formation of dissolved organo-Fe complexes and colloidal organo-Fe oxide phases. Attenuated total reflectance-Fourier transform infrared spectroscopy further confirms the formation of As-Fe-NOM organometallic colloids, however, a detailed study of these types of colloids in natural waters is necessary to underpin their controlling behavior.