Exploring the interference mechanisms of surface and aqueous complexes with groundwater arsenate and arsenite adsorption
Ca 2+ , Mg 2+ , and HCO 3 − are extremely common coexisting ions with arsenic (As) in geogenic As-polluted groundwaters. Although extensive research has improved our knowledge of groundwater As removal techniques and mechanisms, there is still a lack of a definite explanation of the distinct influen...
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creator | Hu, Shan Fu, Jingyi Zhou, Shenmin |
description | Ca
2+
, Mg
2+
, and HCO
3
−
are extremely common coexisting ions with arsenic (As) in geogenic As-polluted groundwaters. Although extensive research has improved our knowledge of groundwater As removal techniques and mechanisms, there is still a lack of a definite explanation of the distinct influences of Ca
2+
and Mg
2+
on As immobilization. Furthermore, the question of whether the occurrence of metal-As aqueous complexes has positive or detrimental effects on As adsorption is still open, which hinders our ability to predict the effectiveness of groundwater As removal. The goal of our present work was to investigate the molecular-level interference mechanisms of Ca
2+
, Mg
2+
, and HCO
3
–
on arsenic adsorption with batch/column filtration experiments and spectroscopic techniques. The results showed that the co-presence of Ca
2+
and As significantly increased As(V) and As(III) adsorption by 22.1 and 12.2% in batch studies and by 20.1 and 16.7% in column adsorptive filtrations, which could be explained by forming a ternary Ca–As–TiO
2
complex. Without the surface complex, Mg
2+
only had a slightly positive effect on As removal. Co-existence of Ca
2+
and HCO
3
−
prevented the generation this surface complex, which significantly decreased the elimination of As(III). Inversely, the As(V) ternary complex and adsorption were not interfered by HCO
3
−
. Moreover, an aqueous Ca–As(V) complex was detected without surface, which facilitated generation of the surface complex and As(V) adsorption. The results of this work clarified the distinct effects of Ca
2+
and Mg
2+
and As(V) and As(III) adsorption, which was critical in predicting the As adsorption efficiency in column filtration processes.
Graphical Abstract |
doi_str_mv | 10.1007/s11356-023-31676-1 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3153613060</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2920985436</sourcerecordid><originalsourceid>FETCH-LOGICAL-c408t-923eccaa2e4297ce3c351121687aa1b7a47ad171ad46cc93cb196e4918f518cb3</originalsourceid><addsrcrecordid>eNqFkVFP3iAUhskyo875B7xYSHazmyoHWiiXi9G5xMQbd0346KlfTQsdtPHz30utzsWL7QY45DkvnDyEnAA7BcbUWQIQlSwYF4UAqWQBH8ghSCgLVWr98a_zAfmU0j1jnGmu9smBqKFmUlaHZHexG_sQO39Hpy3Szk8YW4zoHdIB3db6Lg2JhpamObY231rfUPt7xjAn6sIw9rjDRB-6aUvvYph982BzBrUxoc-nlV-KbimaFOI4dcF_Jnut7RMev-xH5Nflxe35VXF98-Pn-ffrwpWsngrNBTpnLceSa-VQOFEBcJC1shY2ypbKNqDANqV0Tgu3AS2x1FC3FdRuI47ItzV3jCH_Ok1m6JLDvrd-GcEIqIQEwST7L8o1Z1DnRWf06zv0PszR50GeKV1XpZCZ4ivlYkgpYmvG2A02PhpgZlFoVoUmKzTPCg3kpi8v0fNmwOZPy6uzDIgVSOPiDePb2_-IfQJNe6h5</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2920985436</pqid></control><display><type>article</type><title>Exploring the interference mechanisms of surface and aqueous complexes with groundwater arsenate and arsenite adsorption</title><source>SpringerLink Journals - AutoHoldings</source><creator>Hu, Shan ; Fu, Jingyi ; Zhou, Shenmin</creator><creatorcontrib>Hu, Shan ; Fu, Jingyi ; Zhou, Shenmin</creatorcontrib><description>Ca
2+
, Mg
2+
, and HCO
3
−
are extremely common coexisting ions with arsenic (As) in geogenic As-polluted groundwaters. Although extensive research has improved our knowledge of groundwater As removal techniques and mechanisms, there is still a lack of a definite explanation of the distinct influences of Ca
2+
and Mg
2+
on As immobilization. Furthermore, the question of whether the occurrence of metal-As aqueous complexes has positive or detrimental effects on As adsorption is still open, which hinders our ability to predict the effectiveness of groundwater As removal. The goal of our present work was to investigate the molecular-level interference mechanisms of Ca
2+
, Mg
2+
, and HCO
3
–
on arsenic adsorption with batch/column filtration experiments and spectroscopic techniques. The results showed that the co-presence of Ca
2+
and As significantly increased As(V) and As(III) adsorption by 22.1 and 12.2% in batch studies and by 20.1 and 16.7% in column adsorptive filtrations, which could be explained by forming a ternary Ca–As–TiO
2
complex. Without the surface complex, Mg
2+
only had a slightly positive effect on As removal. Co-existence of Ca
2+
and HCO
3
−
prevented the generation this surface complex, which significantly decreased the elimination of As(III). Inversely, the As(V) ternary complex and adsorption were not interfered by HCO
3
−
. Moreover, an aqueous Ca–As(V) complex was detected without surface, which facilitated generation of the surface complex and As(V) adsorption. The results of this work clarified the distinct effects of Ca
2+
and Mg
2+
and As(V) and As(III) adsorption, which was critical in predicting the As adsorption efficiency in column filtration processes.
Graphical Abstract</description><identifier>ISSN: 1614-7499</identifier><identifier>ISSN: 0944-1344</identifier><identifier>EISSN: 1614-7499</identifier><identifier>DOI: 10.1007/s11356-023-31676-1</identifier><identifier>PMID: 38180665</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adsorption ; Adsorptivity ; Aquatic Pollution ; Arsenates ; Arsenic ; Arsenite ; arsenites ; Atmospheric Protection/Air Quality Control/Air Pollution ; Calcium ; Calcium ions ; Earth and Environmental Science ; Ecotoxicology ; Environment ; Environmental Chemistry ; Environmental Health ; Filtration ; Groundwater ; Immobilization ; Interference ; Magnesium ; Research Article ; spectroscopy ; Surface chemistry ; Titanium dioxide ; Waste Water Technology ; Water Management ; Water Pollution Control</subject><ispartof>Environmental science and pollution research international, 2024-02, Vol.31 (6), p.8499-8509</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-923eccaa2e4297ce3c351121687aa1b7a47ad171ad46cc93cb196e4918f518cb3</citedby><cites>FETCH-LOGICAL-c408t-923eccaa2e4297ce3c351121687aa1b7a47ad171ad46cc93cb196e4918f518cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11356-023-31676-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11356-023-31676-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38180665$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Shan</creatorcontrib><creatorcontrib>Fu, Jingyi</creatorcontrib><creatorcontrib>Zhou, Shenmin</creatorcontrib><title>Exploring the interference mechanisms of surface and aqueous complexes with groundwater arsenate and arsenite adsorption</title><title>Environmental science and pollution research international</title><addtitle>Environ Sci Pollut Res</addtitle><addtitle>Environ Sci Pollut Res Int</addtitle><description>Ca
2+
, Mg
2+
, and HCO
3
−
are extremely common coexisting ions with arsenic (As) in geogenic As-polluted groundwaters. Although extensive research has improved our knowledge of groundwater As removal techniques and mechanisms, there is still a lack of a definite explanation of the distinct influences of Ca
2+
and Mg
2+
on As immobilization. Furthermore, the question of whether the occurrence of metal-As aqueous complexes has positive or detrimental effects on As adsorption is still open, which hinders our ability to predict the effectiveness of groundwater As removal. The goal of our present work was to investigate the molecular-level interference mechanisms of Ca
2+
, Mg
2+
, and HCO
3
–
on arsenic adsorption with batch/column filtration experiments and spectroscopic techniques. The results showed that the co-presence of Ca
2+
and As significantly increased As(V) and As(III) adsorption by 22.1 and 12.2% in batch studies and by 20.1 and 16.7% in column adsorptive filtrations, which could be explained by forming a ternary Ca–As–TiO
2
complex. Without the surface complex, Mg
2+
only had a slightly positive effect on As removal. Co-existence of Ca
2+
and HCO
3
−
prevented the generation this surface complex, which significantly decreased the elimination of As(III). Inversely, the As(V) ternary complex and adsorption were not interfered by HCO
3
−
. Moreover, an aqueous Ca–As(V) complex was detected without surface, which facilitated generation of the surface complex and As(V) adsorption. The results of this work clarified the distinct effects of Ca
2+
and Mg
2+
and As(V) and As(III) adsorption, which was critical in predicting the As adsorption efficiency in column filtration processes.
Graphical Abstract</description><subject>Adsorption</subject><subject>Adsorptivity</subject><subject>Aquatic Pollution</subject><subject>Arsenates</subject><subject>Arsenic</subject><subject>Arsenite</subject><subject>arsenites</subject><subject>Atmospheric Protection/Air Quality Control/Air Pollution</subject><subject>Calcium</subject><subject>Calcium ions</subject><subject>Earth and Environmental Science</subject><subject>Ecotoxicology</subject><subject>Environment</subject><subject>Environmental Chemistry</subject><subject>Environmental Health</subject><subject>Filtration</subject><subject>Groundwater</subject><subject>Immobilization</subject><subject>Interference</subject><subject>Magnesium</subject><subject>Research Article</subject><subject>spectroscopy</subject><subject>Surface chemistry</subject><subject>Titanium dioxide</subject><subject>Waste Water Technology</subject><subject>Water Management</subject><subject>Water Pollution Control</subject><issn>1614-7499</issn><issn>0944-1344</issn><issn>1614-7499</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkVFP3iAUhskyo875B7xYSHazmyoHWiiXi9G5xMQbd0346KlfTQsdtPHz30utzsWL7QY45DkvnDyEnAA7BcbUWQIQlSwYF4UAqWQBH8ghSCgLVWr98a_zAfmU0j1jnGmu9smBqKFmUlaHZHexG_sQO39Hpy3Szk8YW4zoHdIB3db6Lg2JhpamObY231rfUPt7xjAn6sIw9rjDRB-6aUvvYph982BzBrUxoc-nlV-KbimaFOI4dcF_Jnut7RMev-xH5Nflxe35VXF98-Pn-ffrwpWsngrNBTpnLceSa-VQOFEBcJC1shY2ypbKNqDANqV0Tgu3AS2x1FC3FdRuI47ItzV3jCH_Ok1m6JLDvrd-GcEIqIQEwST7L8o1Z1DnRWf06zv0PszR50GeKV1XpZCZ4ivlYkgpYmvG2A02PhpgZlFoVoUmKzTPCg3kpi8v0fNmwOZPy6uzDIgVSOPiDePb2_-IfQJNe6h5</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Hu, Shan</creator><creator>Fu, Jingyi</creator><creator>Zhou, Shenmin</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7SN</scope><scope>7T7</scope><scope>7TV</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20240201</creationdate><title>Exploring the interference mechanisms of surface and aqueous complexes with groundwater arsenate and arsenite adsorption</title><author>Hu, Shan ; Fu, Jingyi ; Zhou, Shenmin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-923eccaa2e4297ce3c351121687aa1b7a47ad171ad46cc93cb196e4918f518cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adsorption</topic><topic>Adsorptivity</topic><topic>Aquatic Pollution</topic><topic>Arsenates</topic><topic>Arsenic</topic><topic>Arsenite</topic><topic>arsenites</topic><topic>Atmospheric Protection/Air Quality Control/Air Pollution</topic><topic>Calcium</topic><topic>Calcium ions</topic><topic>Earth and Environmental Science</topic><topic>Ecotoxicology</topic><topic>Environment</topic><topic>Environmental Chemistry</topic><topic>Environmental Health</topic><topic>Filtration</topic><topic>Groundwater</topic><topic>Immobilization</topic><topic>Interference</topic><topic>Magnesium</topic><topic>Research Article</topic><topic>spectroscopy</topic><topic>Surface chemistry</topic><topic>Titanium dioxide</topic><topic>Waste Water Technology</topic><topic>Water Management</topic><topic>Water Pollution Control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Shan</creatorcontrib><creatorcontrib>Fu, Jingyi</creatorcontrib><creatorcontrib>Zhou, Shenmin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Pollution Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Environmental science and pollution research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Shan</au><au>Fu, Jingyi</au><au>Zhou, Shenmin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exploring the interference mechanisms of surface and aqueous complexes with groundwater arsenate and arsenite adsorption</atitle><jtitle>Environmental science and pollution research international</jtitle><stitle>Environ Sci Pollut Res</stitle><addtitle>Environ Sci Pollut Res Int</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>31</volume><issue>6</issue><spage>8499</spage><epage>8509</epage><pages>8499-8509</pages><issn>1614-7499</issn><issn>0944-1344</issn><eissn>1614-7499</eissn><abstract>Ca
2+
, Mg
2+
, and HCO
3
−
are extremely common coexisting ions with arsenic (As) in geogenic As-polluted groundwaters. Although extensive research has improved our knowledge of groundwater As removal techniques and mechanisms, there is still a lack of a definite explanation of the distinct influences of Ca
2+
and Mg
2+
on As immobilization. Furthermore, the question of whether the occurrence of metal-As aqueous complexes has positive or detrimental effects on As adsorption is still open, which hinders our ability to predict the effectiveness of groundwater As removal. The goal of our present work was to investigate the molecular-level interference mechanisms of Ca
2+
, Mg
2+
, and HCO
3
–
on arsenic adsorption with batch/column filtration experiments and spectroscopic techniques. The results showed that the co-presence of Ca
2+
and As significantly increased As(V) and As(III) adsorption by 22.1 and 12.2% in batch studies and by 20.1 and 16.7% in column adsorptive filtrations, which could be explained by forming a ternary Ca–As–TiO
2
complex. Without the surface complex, Mg
2+
only had a slightly positive effect on As removal. Co-existence of Ca
2+
and HCO
3
−
prevented the generation this surface complex, which significantly decreased the elimination of As(III). Inversely, the As(V) ternary complex and adsorption were not interfered by HCO
3
−
. Moreover, an aqueous Ca–As(V) complex was detected without surface, which facilitated generation of the surface complex and As(V) adsorption. The results of this work clarified the distinct effects of Ca
2+
and Mg
2+
and As(V) and As(III) adsorption, which was critical in predicting the As adsorption efficiency in column filtration processes.
Graphical Abstract</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>38180665</pmid><doi>10.1007/s11356-023-31676-1</doi><tpages>11</tpages></addata></record> |
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source | SpringerLink Journals - AutoHoldings |
subjects | Adsorption Adsorptivity Aquatic Pollution Arsenates Arsenic Arsenite arsenites Atmospheric Protection/Air Quality Control/Air Pollution Calcium Calcium ions Earth and Environmental Science Ecotoxicology Environment Environmental Chemistry Environmental Health Filtration Groundwater Immobilization Interference Magnesium Research Article spectroscopy Surface chemistry Titanium dioxide Waste Water Technology Water Management Water Pollution Control |
title | Exploring the interference mechanisms of surface and aqueous complexes with groundwater arsenate and arsenite adsorption |
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