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A Ca MOF combining highly efficient sorption and capability for voltammetric determination of heavy metal ions in aqueous media

We recently discovered that a Ca 2+ two-dimensional framework, namely [Ca(H 4 L)(DMA) 2 ]·2DMA ( Ca-MOF ), was capable of exchanging the Ca 2+ ions with Cu 2+ almost quantitatively in a matter of seconds in aqueous solution. Herein, we report that Ca-MOF exhibits the capability of both removal and v...

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Published in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019-06, Vol.7 (25), p.15432-15443
Main Authors: Pournara, Anastasia D, Margariti, Antigoni, Tarlas, Georgios D, Kourtelaris, Andreas, Petkov, Valeri, Kokkinos, Christos, Economou, Anastasios, Papaefstathiou, Giannis S, Manos, Manolis J
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container_title Journal of materials chemistry. A, Materials for energy and sustainability
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creator Pournara, Anastasia D
Margariti, Antigoni
Tarlas, Georgios D
Kourtelaris, Andreas
Petkov, Valeri
Kokkinos, Christos
Economou, Anastasios
Papaefstathiou, Giannis S
Manos, Manolis J
description We recently discovered that a Ca 2+ two-dimensional framework, namely [Ca(H 4 L)(DMA) 2 ]·2DMA ( Ca-MOF ), was capable of exchanging the Ca 2+ ions with Cu 2+ almost quantitatively in a matter of seconds in aqueous solution. Herein, we report that Ca-MOF exhibits the capability of both removal and voltammetric determination of heavy metal ions in aqueous media. Ca-MOF shows one of the highest Pb 2+ sorption capacities (∼522 mg g −1 ) reported for MOFs. More importantly, a column filled with Ca-MOF (1% wt) particles dispersed in silica sand (99% wt) can quantitatively remove traces of Pb 2+ (∼100 ppb) from a relatively large volume of a wastewater simulant solution (containing a large excess of competitive ions). Ca-MOF is also highly efficient for sorption of Cd 2+ , Ni 2+ and Zn 2+ , even in the presence of several competitive cations. Actually, the Cd 2+ sorption capacity (∼220 mg g −1 ) of Ca-MOF is one of the largest reported for MOFs. Furthermore, detailed Ni 2+ and Zn 2+ sorption studies of MOFs have not been described prior to this work. The mechanism of the M 2+ (M 2+ = Pb 2+ , Cd 2+ , Ni 2+ , Zn 2+ ) exchange process was elucidated based on a series of spectroscopic, analytical and X-ray diffraction methods. In addition, a simple ready-to-use electrochemical sensor based on modified graphite paste with Ca-MOF was fabricated and successfully utilized for the determination of Pb 2+ , Cd 2+ , Cu 2+ and Zn 2+ at μg L −1 levels in aqueous solutions by anodic stripping voltammetry (ASV). Overall, this work demonstrates, for the first time, a dual function of a MOF as a sorbent and as an electrochemical sensor for heavy metal ions, thus opening a new window for materials with application in both environmental remediation and monitoring. The two-dimensional Ca-MOF shows a dual function as a sorbent and an electrochemical sensor for heavy metal ions, which is reported for the first time for a MOF material.
doi_str_mv 10.1039/c9ta03337h
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Herein, we report that Ca-MOF exhibits the capability of both removal and voltammetric determination of heavy metal ions in aqueous media. Ca-MOF shows one of the highest Pb 2+ sorption capacities (∼522 mg g −1 ) reported for MOFs. More importantly, a column filled with Ca-MOF (1% wt) particles dispersed in silica sand (99% wt) can quantitatively remove traces of Pb 2+ (∼100 ppb) from a relatively large volume of a wastewater simulant solution (containing a large excess of competitive ions). Ca-MOF is also highly efficient for sorption of Cd 2+ , Ni 2+ and Zn 2+ , even in the presence of several competitive cations. Actually, the Cd 2+ sorption capacity (∼220 mg g −1 ) of Ca-MOF is one of the largest reported for MOFs. Furthermore, detailed Ni 2+ and Zn 2+ sorption studies of MOFs have not been described prior to this work. The mechanism of the M 2+ (M 2+ = Pb 2+ , Cd 2+ , Ni 2+ , Zn 2+ ) exchange process was elucidated based on a series of spectroscopic, analytical and X-ray diffraction methods. In addition, a simple ready-to-use electrochemical sensor based on modified graphite paste with Ca-MOF was fabricated and successfully utilized for the determination of Pb 2+ , Cd 2+ , Cu 2+ and Zn 2+ at μg L −1 levels in aqueous solutions by anodic stripping voltammetry (ASV). Overall, this work demonstrates, for the first time, a dual function of a MOF as a sorbent and as an electrochemical sensor for heavy metal ions, thus opening a new window for materials with application in both environmental remediation and monitoring. 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A, Materials for energy and sustainability</title><description>We recently discovered that a Ca 2+ two-dimensional framework, namely [Ca(H 4 L)(DMA) 2 ]·2DMA ( Ca-MOF ), was capable of exchanging the Ca 2+ ions with Cu 2+ almost quantitatively in a matter of seconds in aqueous solution. Herein, we report that Ca-MOF exhibits the capability of both removal and voltammetric determination of heavy metal ions in aqueous media. Ca-MOF shows one of the highest Pb 2+ sorption capacities (∼522 mg g −1 ) reported for MOFs. More importantly, a column filled with Ca-MOF (1% wt) particles dispersed in silica sand (99% wt) can quantitatively remove traces of Pb 2+ (∼100 ppb) from a relatively large volume of a wastewater simulant solution (containing a large excess of competitive ions). Ca-MOF is also highly efficient for sorption of Cd 2+ , Ni 2+ and Zn 2+ , even in the presence of several competitive cations. Actually, the Cd 2+ sorption capacity (∼220 mg g −1 ) of Ca-MOF is one of the largest reported for MOFs. Furthermore, detailed Ni 2+ and Zn 2+ sorption studies of MOFs have not been described prior to this work. The mechanism of the M 2+ (M 2+ = Pb 2+ , Cd 2+ , Ni 2+ , Zn 2+ ) exchange process was elucidated based on a series of spectroscopic, analytical and X-ray diffraction methods. In addition, a simple ready-to-use electrochemical sensor based on modified graphite paste with Ca-MOF was fabricated and successfully utilized for the determination of Pb 2+ , Cd 2+ , Cu 2+ and Zn 2+ at μg L −1 levels in aqueous solutions by anodic stripping voltammetry (ASV). Overall, this work demonstrates, for the first time, a dual function of a MOF as a sorbent and as an electrochemical sensor for heavy metal ions, thus opening a new window for materials with application in both environmental remediation and monitoring. 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A, Materials for energy and sustainability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pournara, Anastasia D</au><au>Margariti, Antigoni</au><au>Tarlas, Georgios D</au><au>Kourtelaris, Andreas</au><au>Petkov, Valeri</au><au>Kokkinos, Christos</au><au>Economou, Anastasios</au><au>Papaefstathiou, Giannis S</au><au>Manos, Manolis J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Ca MOF combining highly efficient sorption and capability for voltammetric determination of heavy metal ions in aqueous media</atitle><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle><date>2019-06-25</date><risdate>2019</risdate><volume>7</volume><issue>25</issue><spage>15432</spage><epage>15443</epage><pages>15432-15443</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>We recently discovered that a Ca 2+ two-dimensional framework, namely [Ca(H 4 L)(DMA) 2 ]·2DMA ( Ca-MOF ), was capable of exchanging the Ca 2+ ions with Cu 2+ almost quantitatively in a matter of seconds in aqueous solution. Herein, we report that Ca-MOF exhibits the capability of both removal and voltammetric determination of heavy metal ions in aqueous media. Ca-MOF shows one of the highest Pb 2+ sorption capacities (∼522 mg g −1 ) reported for MOFs. More importantly, a column filled with Ca-MOF (1% wt) particles dispersed in silica sand (99% wt) can quantitatively remove traces of Pb 2+ (∼100 ppb) from a relatively large volume of a wastewater simulant solution (containing a large excess of competitive ions). Ca-MOF is also highly efficient for sorption of Cd 2+ , Ni 2+ and Zn 2+ , even in the presence of several competitive cations. Actually, the Cd 2+ sorption capacity (∼220 mg g −1 ) of Ca-MOF is one of the largest reported for MOFs. Furthermore, detailed Ni 2+ and Zn 2+ sorption studies of MOFs have not been described prior to this work. The mechanism of the M 2+ (M 2+ = Pb 2+ , Cd 2+ , Ni 2+ , Zn 2+ ) exchange process was elucidated based on a series of spectroscopic, analytical and X-ray diffraction methods. In addition, a simple ready-to-use electrochemical sensor based on modified graphite paste with Ca-MOF was fabricated and successfully utilized for the determination of Pb 2+ , Cd 2+ , Cu 2+ and Zn 2+ at μg L −1 levels in aqueous solutions by anodic stripping voltammetry (ASV). Overall, this work demonstrates, for the first time, a dual function of a MOF as a sorbent and as an electrochemical sensor for heavy metal ions, thus opening a new window for materials with application in both environmental remediation and monitoring. The two-dimensional Ca-MOF shows a dual function as a sorbent and an electrochemical sensor for heavy metal ions, which is reported for the first time for a MOF material.</abstract><doi>10.1039/c9ta03337h</doi><tpages>12</tpages></addata></record>
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title A Ca MOF combining highly efficient sorption and capability for voltammetric determination of heavy metal ions in aqueous media
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