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Kip, Cigdem; Erkakan, Damla; Gokaltun, Aslihan; Celebi, Bekir; Tuncel, Ali
<?xml version='1.0' encoding='utf-8'?> <resource xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd"> <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/82947</identifier> <creators> <creator> <creatorName>Kip, Cigdem</creatorName> <givenName>Cigdem</givenName> <familyName>Kip</familyName> <affiliation>Hacettepe Univ, Dept Chem Engn, TR-06532 Ankara, Turkey</affiliation> </creator> <creator> <creatorName>Erkakan, Damla</creatorName> <givenName>Damla</givenName> <familyName>Erkakan</familyName> <affiliation>Hacettepe Univ, Dept Chem Engn, TR-06532 Ankara, Turkey</affiliation> </creator> <creator> <creatorName>Gokaltun, Aslihan</creatorName> <givenName>Aslihan</givenName> <familyName>Gokaltun</familyName> <affiliation>Hacettepe Univ, Dept Chem Engn, TR-06532 Ankara, Turkey</affiliation> </creator> <creator> <creatorName>Celebi, Bekir</creatorName> <givenName>Bekir</givenName> <familyName>Celebi</familyName> <affiliation>Hacettepe Univ, Dept Chem Engn, TR-06532 Ankara, Turkey</affiliation> </creator> <creator> <creatorName>Tuncel, Ali</creatorName> <givenName>Ali</givenName> <familyName>Tuncel</familyName> </creator> </creators> <titles> <title>Synthesis Of A Reactive Polymethacrylate Capillary Monolith And Its Use As A Starting Material For The Preparation Of A Stationary Phase For Hydrophilic Interaction Chromatography</title> </titles> <publisher>Aperta</publisher> <publicationYear>2015</publicationYear> <dates> <date dateType="Issued">2015-01-01</date> </dates> <resourceType resourceTypeGeneral="Text">Journal article</resourceType> <alternateIdentifiers> <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/82947</alternateIdentifier> </alternateIdentifiers> <relatedIdentifiers> <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1016/j.chroma.2015.04.005</relatedIdentifier> </relatedIdentifiers> <rightsList> <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights> <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights> </rightsList> <descriptions> <description descriptionType="Abstract">Poly(3-chloro-2-hydroxypropyl methacrylate-co-ethylene dimethacrylate), poly(HPMA-Cl-co-EDMA) capillary monolith was proposed as a reactive starting material with tailoring flexibility for the preparation of monolithic stationary phases. The reactive capillary monolith was synthesized by free radical copolymerization of 3-chloro-2-hydroxypropyl methacrylate (HPMA-Cl) and ethylene dimethacrylate (EDMA). The mean pore size, the specific surface area and the permeability of poly(HPMA-Cl-co-EDMA) monoliths were controlled by adjusting porogen/monomer volume ratio, porogen composition and polymerization temperature. The porogen/monomer volume ratio was found as the most effective factor controlling the porous properties of poly(HPMA-Cl-co-EDMA) monolith. Triethanolamine (TEA-OH) functionalized polymethacrylate monoliths were prepared by using the reactive chloropropyl group of poly(HPMA-Cl-co-EDMA) monolith via one-pot and simple post-functionalization process. Poly(HPMA-Cl-co-EDMA) monolith reacted with TEA-OH was evaluated as a stationary phase in nano-hydrophilic interaction chromatography (nano-HILIC). Nucleotides, nucleosides and benzoic acid derivatives were satisfactorily separated with the plate heights up to 20 mu m. TEA-OH attached-poly(HPMA-Cl-co-EDIVIA) monolith showed a reproducible and stable retention behaviour in nano-HILIC runs. However, a decrease in the column performance (i.e. an increase in the plate height) was observed with the increasing retention factor. Hence "retention-dependent column efficiency" behaviour was shown for HILIC mode using the chromatographic data collected with the polymer based monolith synthesized. (C) 2015 Elsevier B.V. All rights reserved.</description> </descriptions> </resource>
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