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Synthesis, characterization and applications of immobilized iminodiacetic acid-modified silica
Porous immobilized iminodiacetic acid modified silica of the general formula S—(CH2)3—N(CH2COOH)2, (where S represents [Si—O]n siloxane network) has been prepared by replacement of the iodide in 3-iodopropyl modified silica with diethyliminodiacetate. The immobilized-diethyliminodiacetate ligand sys...
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Published in: | Journal of sol-gel science and technology 2003-09, Vol.28 (2), p.255-265 |
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creator | EL-NAHHAL, Issa M ZAGGOUT, Farid R NASSAR, Mona A EL-ASHGAR, Nizam M MAQUET, Jocelyne BABONNEAU, Florence CHEHIMI, Mohamed M |
description | Porous immobilized iminodiacetic acid modified silica of the general formula S—(CH2)3—N(CH2COOH)2, (where S represents [Si—O]n siloxane network) has been prepared by replacement of the iodide in 3-iodopropyl modified silica with diethyliminodiacetate. The immobilized-diethyliminodiacetate ligand system (S-DIDA) was then hydrolyzed by hydrochloric acid to produce the immobilized iminodiacetic acid ligand system (S-IDA). The iodo functionalized modified silica (S-I) was prepared by polycondensation of Si(OEt)4 and (MeO)3Si(CH2)3I. The XPS and CP/MAS 13C NMR spectra showed that not all iodine atoms are replaced and that the hydrolysis of ethyl acetate groups are incomplete upon treatment with HCl. The immobilized iminodiacetic acid ligand system exhibits high potential for the uptake of various di- and trivalent metal ions such as (Mn2+, Fe3+, Co2+, Ni2+, Cu2+ and Zn2+). Complexation of the iminodiacetate ligand system for the metal ions at the optimum conditions was found in the order: Cu2+ > Fe3+ > Ni2+ > Co2+ > Mn2+ > Zn2+. Stability studies of the iminodiacetate ligand system showed that a degradation of the siloxane network and leaching of some species occurred upon treatment with strong acid and base aqueous solutions. |
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The immobilized-diethyliminodiacetate ligand system (S-DIDA) was then hydrolyzed by hydrochloric acid to produce the immobilized iminodiacetic acid ligand system (S-IDA). The iodo functionalized modified silica (S-I) was prepared by polycondensation of Si(OEt)4 and (MeO)3Si(CH2)3I. The XPS and CP/MAS 13C NMR spectra showed that not all iodine atoms are replaced and that the hydrolysis of ethyl acetate groups are incomplete upon treatment with HCl. The immobilized iminodiacetic acid ligand system exhibits high potential for the uptake of various di- and trivalent metal ions such as (Mn2+, Fe3+, Co2+, Ni2+, Cu2+ and Zn2+). Complexation of the iminodiacetate ligand system for the metal ions at the optimum conditions was found in the order: Cu2+ > Fe3+ > Ni2+ > Co2+ > Mn2+ > Zn2+. Stability studies of the iminodiacetate ligand system showed that a degradation of the siloxane network and leaching of some species occurred upon treatment with strong acid and base aqueous solutions.</description><identifier>ISSN: 0928-0707</identifier><identifier>EISSN: 1573-4846</identifier><identifier>DOI: 10.1023/A:1026093419515</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Aqueous solutions ; Chemistry ; Cobalt ; Colloidal gels. Colloidal sols ; Colloidal state and disperse state ; Copper ; Ethyl acetate ; Exact sciences and technology ; Ferric ions ; General and physical chemistry ; Hydrochloric acid ; Iodine ; Leaching ; Ligands ; Manganese ions ; Metal ions ; Nickel ; NMR ; Nuclear magnetic resonance ; Silicon dioxide ; X ray photoelectron spectroscopy</subject><ispartof>Journal of sol-gel science and technology, 2003-09, Vol.28 (2), p.255-265</ispartof><rights>2004 INIST-CNRS</rights><rights>Journal of Sol-Gel Science and Technology is a copyright of Springer, (2003). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c257t-e9382673ba9730204bb036d824187369d264f03c6a3f911f575c0bccd9ebd81b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15246707$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>EL-NAHHAL, Issa M</creatorcontrib><creatorcontrib>ZAGGOUT, Farid R</creatorcontrib><creatorcontrib>NASSAR, Mona A</creatorcontrib><creatorcontrib>EL-ASHGAR, Nizam M</creatorcontrib><creatorcontrib>MAQUET, Jocelyne</creatorcontrib><creatorcontrib>BABONNEAU, Florence</creatorcontrib><creatorcontrib>CHEHIMI, Mohamed M</creatorcontrib><title>Synthesis, characterization and applications of immobilized iminodiacetic acid-modified silica</title><title>Journal of sol-gel science and technology</title><description>Porous immobilized iminodiacetic acid modified silica of the general formula S—(CH2)3—N(CH2COOH)2, (where S represents [Si—O]n siloxane network) has been prepared by replacement of the iodide in 3-iodopropyl modified silica with diethyliminodiacetate. The immobilized-diethyliminodiacetate ligand system (S-DIDA) was then hydrolyzed by hydrochloric acid to produce the immobilized iminodiacetic acid ligand system (S-IDA). The iodo functionalized modified silica (S-I) was prepared by polycondensation of Si(OEt)4 and (MeO)3Si(CH2)3I. The XPS and CP/MAS 13C NMR spectra showed that not all iodine atoms are replaced and that the hydrolysis of ethyl acetate groups are incomplete upon treatment with HCl. The immobilized iminodiacetic acid ligand system exhibits high potential for the uptake of various di- and trivalent metal ions such as (Mn2+, Fe3+, Co2+, Ni2+, Cu2+ and Zn2+). Complexation of the iminodiacetate ligand system for the metal ions at the optimum conditions was found in the order: Cu2+ > Fe3+ > Ni2+ > Co2+ > Mn2+ > Zn2+. Stability studies of the iminodiacetate ligand system showed that a degradation of the siloxane network and leaching of some species occurred upon treatment with strong acid and base aqueous solutions.</description><subject>Aqueous solutions</subject><subject>Chemistry</subject><subject>Cobalt</subject><subject>Colloidal gels. Colloidal sols</subject><subject>Colloidal state and disperse state</subject><subject>Copper</subject><subject>Ethyl acetate</subject><subject>Exact sciences and technology</subject><subject>Ferric ions</subject><subject>General and physical chemistry</subject><subject>Hydrochloric acid</subject><subject>Iodine</subject><subject>Leaching</subject><subject>Ligands</subject><subject>Manganese ions</subject><subject>Metal ions</subject><subject>Nickel</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Silicon dioxide</subject><subject>X ray photoelectron spectroscopy</subject><issn>0928-0707</issn><issn>1573-4846</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNotkElLA0EQhRtRMEbPXgfEm6O997S3EOICAQ_q1aG3IRVms3tySH69reb03uN9VQWF0DXB9wRT9rB4zCKxZpxoQcQJmhGhWMkrLk_RDGtalVhhdY4uUtpijAUnaoa-3vf9tAkJ0l3hNiYaN4UIBzPB0Bem94UZxxbcX07F0BTQdYOFFg7BZw_94MG4MIErjANfdjk3kLsEv2OX6KwxbQpXR52jz6fVx_KlXL89vy4X69JRoaYyaFZRqZg1WjFMMbcWM-krykmlmNSeSt5g5qRhjSakEUo4bJ3zOlhfEcvm6OZ_7xiH711IU70ddrHPJ2tKhRaSVoJm6vZImeRM20TTO0j1GKEzcV8TQbnML2I_tkhjLw</recordid><startdate>20030901</startdate><enddate>20030901</enddate><creator>EL-NAHHAL, Issa M</creator><creator>ZAGGOUT, Farid R</creator><creator>NASSAR, Mona A</creator><creator>EL-ASHGAR, Nizam M</creator><creator>MAQUET, Jocelyne</creator><creator>BABONNEAU, Florence</creator><creator>CHEHIMI, Mohamed M</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>L6V</scope><scope>M7S</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope></search><sort><creationdate>20030901</creationdate><title>Synthesis, characterization and applications of immobilized iminodiacetic acid-modified silica</title><author>EL-NAHHAL, Issa M ; ZAGGOUT, Farid R ; NASSAR, Mona A ; EL-ASHGAR, Nizam M ; MAQUET, Jocelyne ; BABONNEAU, Florence ; CHEHIMI, Mohamed M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c257t-e9382673ba9730204bb036d824187369d264f03c6a3f911f575c0bccd9ebd81b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Aqueous solutions</topic><topic>Chemistry</topic><topic>Cobalt</topic><topic>Colloidal gels. Colloidal sols</topic><topic>Colloidal state and disperse state</topic><topic>Copper</topic><topic>Ethyl acetate</topic><topic>Exact sciences and technology</topic><topic>Ferric ions</topic><topic>General and physical chemistry</topic><topic>Hydrochloric acid</topic><topic>Iodine</topic><topic>Leaching</topic><topic>Ligands</topic><topic>Manganese ions</topic><topic>Metal ions</topic><topic>Nickel</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Silicon dioxide</topic><topic>X ray photoelectron spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>EL-NAHHAL, Issa M</creatorcontrib><creatorcontrib>ZAGGOUT, Farid R</creatorcontrib><creatorcontrib>NASSAR, Mona A</creatorcontrib><creatorcontrib>EL-ASHGAR, Nizam M</creatorcontrib><creatorcontrib>MAQUET, Jocelyne</creatorcontrib><creatorcontrib>BABONNEAU, Florence</creatorcontrib><creatorcontrib>CHEHIMI, Mohamed M</creatorcontrib><collection>Pascal-Francis</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>ProQuest Engineering Collection</collection><collection>Engineering Database</collection><collection>Materials science collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><jtitle>Journal of sol-gel science and technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>EL-NAHHAL, Issa M</au><au>ZAGGOUT, Farid R</au><au>NASSAR, Mona A</au><au>EL-ASHGAR, Nizam M</au><au>MAQUET, Jocelyne</au><au>BABONNEAU, Florence</au><au>CHEHIMI, Mohamed M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, characterization and applications of immobilized iminodiacetic acid-modified silica</atitle><jtitle>Journal of sol-gel science and technology</jtitle><date>2003-09-01</date><risdate>2003</risdate><volume>28</volume><issue>2</issue><spage>255</spage><epage>265</epage><pages>255-265</pages><issn>0928-0707</issn><eissn>1573-4846</eissn><abstract>Porous immobilized iminodiacetic acid modified silica of the general formula S—(CH2)3—N(CH2COOH)2, (where S represents [Si—O]n siloxane network) has been prepared by replacement of the iodide in 3-iodopropyl modified silica with diethyliminodiacetate. The immobilized-diethyliminodiacetate ligand system (S-DIDA) was then hydrolyzed by hydrochloric acid to produce the immobilized iminodiacetic acid ligand system (S-IDA). The iodo functionalized modified silica (S-I) was prepared by polycondensation of Si(OEt)4 and (MeO)3Si(CH2)3I. The XPS and CP/MAS 13C NMR spectra showed that not all iodine atoms are replaced and that the hydrolysis of ethyl acetate groups are incomplete upon treatment with HCl. The immobilized iminodiacetic acid ligand system exhibits high potential for the uptake of various di- and trivalent metal ions such as (Mn2+, Fe3+, Co2+, Ni2+, Cu2+ and Zn2+). Complexation of the iminodiacetate ligand system for the metal ions at the optimum conditions was found in the order: Cu2+ > Fe3+ > Ni2+ > Co2+ > Mn2+ > Zn2+. Stability studies of the iminodiacetate ligand system showed that a degradation of the siloxane network and leaching of some species occurred upon treatment with strong acid and base aqueous solutions.</abstract><cop>Heidelberg</cop><pub>Springer</pub><doi>10.1023/A:1026093419515</doi><tpages>11</tpages></addata></record> |
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subjects | Aqueous solutions Chemistry Cobalt Colloidal gels. Colloidal sols Colloidal state and disperse state Copper Ethyl acetate Exact sciences and technology Ferric ions General and physical chemistry Hydrochloric acid Iodine Leaching Ligands Manganese ions Metal ions Nickel NMR Nuclear magnetic resonance Silicon dioxide X ray photoelectron spectroscopy |
title | Synthesis, characterization and applications of immobilized iminodiacetic acid-modified silica |
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