Cs desorption behavior during hydrothermal treatment of illite with oxalic acid

The desorption of radioactive cesium (Cs) in soil is influenced by the clay mineral type, adsorption site, and concentration of Cs. In this study, experiments to detect desorption of non-radioactive and radioactive Cs from illite using oxalic acid were performed for 2 days at 70 °C in hydrothermal c...

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Veröffentlicht in:Environmental science and pollution research international 2020-10, Vol.27 (28), p.35580-35590
Hauptverfasser: Kim, Sung-Man, Yoon, In-Ho, Kim, Il-Gook, Park, Chan Woo, Sihn, YoungHo, Kim, June-Hyun, Park, So-Jin
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container_issue 28
container_start_page 35580
container_title Environmental science and pollution research international
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creator Kim, Sung-Man
Yoon, In-Ho
Kim, Il-Gook
Park, Chan Woo
Sihn, YoungHo
Kim, June-Hyun
Park, So-Jin
description The desorption of radioactive cesium (Cs) in soil is influenced by the clay mineral type, adsorption site, and concentration of Cs. In this study, experiments to detect desorption of non-radioactive and radioactive Cs from illite using oxalic acid were performed for 2 days at 70 °C in hydrothermal conditions. The results showed that the 133 Cs removal efficiency by oxalic acid and inorganic acid treatment was similar at high concentration (22.86 mmol/kg) of non-radioactive 133 Cs. In the radioactive 137 Cs experiment, the removal efficiency by oxalic acid was higher than that by inorganic acid at low concentration (0.79 × 10 −6  mmol/kg) of radioactive 137 Cs. Based on the illite hypothetical frayed edge site (FES) concentration of 0.612 mmol/kg, the results suggested that 137 Cs was preferentially adsorbed to FES on illite. The 137 Cs at low concentration was difficult to remove because it was irreversible adsorption to FES, while the non-radioactive Cs at high concentration was mainly adsorbed to planar sites, and so was easy to desorb by ion exchange. Based on the results of NMR, FTIR, and XPS analyses, we concluded that the higher efficiency of 137 Cs removal at low concentration by oxalic acid treatment than by treatment with inorganic acid was because of chelation effects associated with the complexation of oxalic acid (ligands) and metal ions in irreversible site (FES).
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In this study, experiments to detect desorption of non-radioactive and radioactive Cs from illite using oxalic acid were performed for 2 days at 70 °C in hydrothermal conditions. The results showed that the 133 Cs removal efficiency by oxalic acid and inorganic acid treatment was similar at high concentration (22.86 mmol/kg) of non-radioactive 133 Cs. In the radioactive 137 Cs experiment, the removal efficiency by oxalic acid was higher than that by inorganic acid at low concentration (0.79 × 10 −6  mmol/kg) of radioactive 137 Cs. Based on the illite hypothetical frayed edge site (FES) concentration of 0.612 mmol/kg, the results suggested that 137 Cs was preferentially adsorbed to FES on illite. The 137 Cs at low concentration was difficult to remove because it was irreversible adsorption to FES, while the non-radioactive Cs at high concentration was mainly adsorbed to planar sites, and so was easy to desorb by ion exchange. Based on the results of NMR, FTIR, and XPS analyses, we concluded that the higher efficiency of 137 Cs removal at low concentration by oxalic acid treatment than by treatment with inorganic acid was because of chelation effects associated with the complexation of oxalic acid (ligands) and metal ions in irreversible site (FES).</description><identifier>ISSN: 0944-1344</identifier><identifier>EISSN: 1614-7499</identifier><identifier>DOI: 10.1007/s11356-020-09675-3</identifier><identifier>PMID: 32594435</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Acids ; Adsorption ; Aquatic Pollution ; Atmospheric Protection/Air Quality Control/Air Pollution ; Cesium ; Cesium 133 ; Cesium 137 ; Cesium isotopes ; Cesium radioisotopes ; Chelation ; Clay minerals ; Desorption ; Earth and Environmental Science ; Ecotoxicology ; Efficiency ; Environment ; Environmental Chemistry ; Environmental Health ; Environmental science ; Hydrothermal treatment ; Illite ; Inorganic acids ; Ion exchange ; Metal ions ; Minerals ; NMR ; Nuclear magnetic resonance ; Oxalic Acid ; Research Article ; Waste Water Technology ; Water Management ; Water Pollutants, Radioactive - analysis ; Water Pollution Control ; X ray photoelectron spectroscopy</subject><ispartof>Environmental science and pollution research international, 2020-10, Vol.27 (28), p.35580-35590</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-4964fc211c7dd6526ea08a3ce0f2e3945a51545481feabb75618a70cc3f2ecd93</citedby><cites>FETCH-LOGICAL-c412t-4964fc211c7dd6526ea08a3ce0f2e3945a51545481feabb75618a70cc3f2ecd93</cites><orcidid>0000-0001-8740-0573</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11356-020-09675-3$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11356-020-09675-3$$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/32594435$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Sung-Man</creatorcontrib><creatorcontrib>Yoon, In-Ho</creatorcontrib><creatorcontrib>Kim, Il-Gook</creatorcontrib><creatorcontrib>Park, Chan Woo</creatorcontrib><creatorcontrib>Sihn, YoungHo</creatorcontrib><creatorcontrib>Kim, June-Hyun</creatorcontrib><creatorcontrib>Park, So-Jin</creatorcontrib><title>Cs desorption behavior during hydrothermal treatment of illite with oxalic acid</title><title>Environmental science and pollution research international</title><addtitle>Environ Sci Pollut Res</addtitle><addtitle>Environ Sci Pollut Res Int</addtitle><description>The desorption of radioactive cesium (Cs) in soil is influenced by the clay mineral type, adsorption site, and concentration of Cs. In this study, experiments to detect desorption of non-radioactive and radioactive Cs from illite using oxalic acid were performed for 2 days at 70 °C in hydrothermal conditions. The results showed that the 133 Cs removal efficiency by oxalic acid and inorganic acid treatment was similar at high concentration (22.86 mmol/kg) of non-radioactive 133 Cs. In the radioactive 137 Cs experiment, the removal efficiency by oxalic acid was higher than that by inorganic acid at low concentration (0.79 × 10 −6  mmol/kg) of radioactive 137 Cs. Based on the illite hypothetical frayed edge site (FES) concentration of 0.612 mmol/kg, the results suggested that 137 Cs was preferentially adsorbed to FES on illite. The 137 Cs at low concentration was difficult to remove because it was irreversible adsorption to FES, while the non-radioactive Cs at high concentration was mainly adsorbed to planar sites, and so was easy to desorb by ion exchange. Based on the results of NMR, FTIR, and XPS analyses, we concluded that the higher efficiency of 137 Cs removal at low concentration by oxalic acid treatment than by treatment with inorganic acid was because of chelation effects associated with the complexation of oxalic acid (ligands) and metal ions in irreversible site (FES).</description><subject>Acids</subject><subject>Adsorption</subject><subject>Aquatic Pollution</subject><subject>Atmospheric Protection/Air Quality Control/Air Pollution</subject><subject>Cesium</subject><subject>Cesium 133</subject><subject>Cesium 137</subject><subject>Cesium isotopes</subject><subject>Cesium radioisotopes</subject><subject>Chelation</subject><subject>Clay minerals</subject><subject>Desorption</subject><subject>Earth and Environmental Science</subject><subject>Ecotoxicology</subject><subject>Efficiency</subject><subject>Environment</subject><subject>Environmental Chemistry</subject><subject>Environmental Health</subject><subject>Environmental science</subject><subject>Hydrothermal treatment</subject><subject>Illite</subject><subject>Inorganic acids</subject><subject>Ion exchange</subject><subject>Metal ions</subject><subject>Minerals</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Oxalic Acid</subject><subject>Research Article</subject><subject>Waste Water Technology</subject><subject>Water Management</subject><subject>Water Pollutants, Radioactive - analysis</subject><subject>Water Pollution Control</subject><subject>X ray photoelectron spectroscopy</subject><issn>0944-1344</issn><issn>1614-7499</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kL1OwzAYRS0EoqXwAgzIEnPA_6lHVPEnIXWB2XIch7hK4mA7QN-elBTYmL7hnns_6QBwjtEVRii_jhhTLjJEUIakyHlGD8AcC8yynEl5COZIMpZhytgMnMS4QSMpSX4MZpTwMaJ8DtarCEsbfeiT8x0sbK3fnQ-wHILrXmG9LYNPtQ2tbmAKVqfWdgn6CrqmccnCD5dq6D914wzUxpWn4KjSTbRn-7sAL3e3z6uH7Gl9_7i6ecoMwyRlTApWGYKxyctScCKsRktNjUUVsVQyrjnmjLMlrqwuipwLvNQ5MoaOuSklXYDLabcP_m2wMamNH0I3vlSEUSFzQZY7ikyUCT7GYCvVB9fqsFUYqZ1DNTlUoxn17VDRsXSxnx6K1pa_lR9pI0AnIPY7STb8_f5n9guFsXzb</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Kim, Sung-Man</creator><creator>Yoon, In-Ho</creator><creator>Kim, Il-Gook</creator><creator>Park, Chan Woo</creator><creator>Sihn, YoungHo</creator><creator>Kim, June-Hyun</creator><creator>Park, So-Jin</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7SN</scope><scope>7T7</scope><scope>7TV</scope><scope>7U7</scope><scope>7WY</scope><scope>7WZ</scope><scope>7X7</scope><scope>7XB</scope><scope>87Z</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FL</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BEZIV</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FRNLG</scope><scope>FYUFA</scope><scope>F~G</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K60</scope><scope>K6~</scope><scope>K9.</scope><scope>L.-</scope><scope>M0C</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>P64</scope><scope>PATMY</scope><scope>PQBIZ</scope><scope>PQBZA</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>Q9U</scope><orcidid>https://orcid.org/0000-0001-8740-0573</orcidid></search><sort><creationdate>20201001</creationdate><title>Cs desorption behavior during hydrothermal treatment of illite with oxalic acid</title><author>Kim, Sung-Man ; 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In this study, experiments to detect desorption of non-radioactive and radioactive Cs from illite using oxalic acid were performed for 2 days at 70 °C in hydrothermal conditions. The results showed that the 133 Cs removal efficiency by oxalic acid and inorganic acid treatment was similar at high concentration (22.86 mmol/kg) of non-radioactive 133 Cs. In the radioactive 137 Cs experiment, the removal efficiency by oxalic acid was higher than that by inorganic acid at low concentration (0.79 × 10 −6  mmol/kg) of radioactive 137 Cs. Based on the illite hypothetical frayed edge site (FES) concentration of 0.612 mmol/kg, the results suggested that 137 Cs was preferentially adsorbed to FES on illite. The 137 Cs at low concentration was difficult to remove because it was irreversible adsorption to FES, while the non-radioactive Cs at high concentration was mainly adsorbed to planar sites, and so was easy to desorb by ion exchange. Based on the results of NMR, FTIR, and XPS analyses, we concluded that the higher efficiency of 137 Cs removal at low concentration by oxalic acid treatment than by treatment with inorganic acid was because of chelation effects associated with the complexation of oxalic acid (ligands) and metal ions in irreversible site (FES).</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32594435</pmid><doi>10.1007/s11356-020-09675-3</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-8740-0573</orcidid></addata></record>
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subjects Acids
Adsorption
Aquatic Pollution
Atmospheric Protection/Air Quality Control/Air Pollution
Cesium
Cesium 133
Cesium 137
Cesium isotopes
Cesium radioisotopes
Chelation
Clay minerals
Desorption
Earth and Environmental Science
Ecotoxicology
Efficiency
Environment
Environmental Chemistry
Environmental Health
Environmental science
Hydrothermal treatment
Illite
Inorganic acids
Ion exchange
Metal ions
Minerals
NMR
Nuclear magnetic resonance
Oxalic Acid
Research Article
Waste Water Technology
Water Management
Water Pollutants, Radioactive - analysis
Water Pollution Control
X ray photoelectron spectroscopy
title Cs desorption behavior during hydrothermal treatment of illite with oxalic acid
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