Preparation and characterization of mono- and multilayer films of polymerizable 1,2-polybutadiene using the Langmuir-Blodgett technique.
Identifieur interne : 001197 ( Main/Exploration ); précédent : 001196; suivant : 001198Preparation and characterization of mono- and multilayer films of polymerizable 1,2-polybutadiene using the Langmuir-Blodgett technique.
Auteurs : RBID : pubmed:21863826English descriptors
- KwdEn :
- MESH :
- chemical , chemical synthesis : Butadienes, Elastomers.
- chemical , chemistry : Butadienes, Elastomers, Gold, Silicon, Tin Compounds.
- chemical : Membranes, Artificial.
- Particle Size, Surface Properties.
Abstract
The essence of this study is to apply the Langmuir-Blodgett (LB) technique for assembling asymmetric membranes. Accordingly, Langmuir films of a (further) polymerizable polymer, 1,2-polybutadiene (1,2-pbd), were studied and transferred onto different solid supports, such as gold, indium tin oxide (ITO), and silicon. The layers were characterized both at the air/water interface as well as on different substrates using numerous methods including cyclic voltammetry, impedance spectroscopy, spectroscopic ellipsometry, atomic force microscopy, X-ray photoelectron spectroscopy, and reflection-absorption Fourier transform infrared spectroscopy. The Langmuir films were stable at the air-water interface as long as they were not exposed to UV irradiation. The LB films formed disorganized layers, which gradually blocked the permeation of different species with increasing the number of deposited layers. The thickness was ca. 4-7 Å per layer. Irradiating the Langmuir films caused their cross-linking at the air-water interface. Furthermore, we took advantage of the reactivity of the double bond of the LB films on the solid supports and graft polymerized acrylic acid on top of the 1,2-pbd layers. This approach is the basis of the formation of an asymmetric membrane that requires different porosity on both of its sides.
DOI: 10.1021/la201534e
PubMed: 21863826
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Le document en format XML
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<author><name sortKey="Hitrik, Maria" uniqKey="Hitrik M">Maria Hitrik</name>
<affiliation wicri:level="1"><nlm:affiliation>Institute of Chemistry, the Hebrew University of Jerusalem, Jerusalem 91904, Israel.</nlm:affiliation>
<country xml:lang="fr">Israël</country>
<wicri:regionArea>Institute of Chemistry, the Hebrew University of Jerusalem, Jerusalem 91904</wicri:regionArea>
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<author><name sortKey="Gutkin, Vitaly" uniqKey="Gutkin V">Vitaly Gutkin</name>
</author>
<author><name sortKey="Lev, Ovadia" uniqKey="Lev O">Ovadia Lev</name>
</author>
<author><name sortKey="Mandler, Daniel" uniqKey="Mandler D">Daniel Mandler</name>
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<term>Butadienes (chemistry)</term>
<term>Elastomers (chemical synthesis)</term>
<term>Elastomers (chemistry)</term>
<term>Gold (chemistry)</term>
<term>Membranes, Artificial</term>
<term>Particle Size</term>
<term>Silicon (chemistry)</term>
<term>Surface Properties</term>
<term>Tin Compounds (chemistry)</term>
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<keywords scheme="MESH" type="chemical" qualifier="chemical synthesis" xml:lang="en"><term>Butadienes</term>
<term>Elastomers</term>
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<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Butadienes</term>
<term>Elastomers</term>
<term>Gold</term>
<term>Silicon</term>
<term>Tin Compounds</term>
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<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Membranes, Artificial</term>
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<front><div type="abstract" xml:lang="en">The essence of this study is to apply the Langmuir-Blodgett (LB) technique for assembling asymmetric membranes. Accordingly, Langmuir films of a (further) polymerizable polymer, 1,2-polybutadiene (1,2-pbd), were studied and transferred onto different solid supports, such as gold, indium tin oxide (ITO), and silicon. The layers were characterized both at the air/water interface as well as on different substrates using numerous methods including cyclic voltammetry, impedance spectroscopy, spectroscopic ellipsometry, atomic force microscopy, X-ray photoelectron spectroscopy, and reflection-absorption Fourier transform infrared spectroscopy. The Langmuir films were stable at the air-water interface as long as they were not exposed to UV irradiation. The LB films formed disorganized layers, which gradually blocked the permeation of different species with increasing the number of deposited layers. The thickness was ca. 4-7 Å per layer. Irradiating the Langmuir films caused their cross-linking at the air-water interface. Furthermore, we took advantage of the reactivity of the double bond of the LB films on the solid supports and graft polymerized acrylic acid on top of the 1,2-pbd layers. This approach is the basis of the formation of an asymmetric membrane that requires different porosity on both of its sides.</div>
</front>
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<DateRevised><Year>2013</Year>
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<Issue>19</Issue>
<PubDate><Year>2011</Year>
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<Day>4</Day>
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<Title>Langmuir : the ACS journal of surfaces and colloids</Title>
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<ArticleTitle>Preparation and characterization of mono- and multilayer films of polymerizable 1,2-polybutadiene using the Langmuir-Blodgett technique.</ArticleTitle>
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<Abstract><AbstractText>The essence of this study is to apply the Langmuir-Blodgett (LB) technique for assembling asymmetric membranes. Accordingly, Langmuir films of a (further) polymerizable polymer, 1,2-polybutadiene (1,2-pbd), were studied and transferred onto different solid supports, such as gold, indium tin oxide (ITO), and silicon. The layers were characterized both at the air/water interface as well as on different substrates using numerous methods including cyclic voltammetry, impedance spectroscopy, spectroscopic ellipsometry, atomic force microscopy, X-ray photoelectron spectroscopy, and reflection-absorption Fourier transform infrared spectroscopy. The Langmuir films were stable at the air-water interface as long as they were not exposed to UV irradiation. The LB films formed disorganized layers, which gradually blocked the permeation of different species with increasing the number of deposited layers. The thickness was ca. 4-7 Å per layer. Irradiating the Langmuir films caused their cross-linking at the air-water interface. Furthermore, we took advantage of the reactivity of the double bond of the LB films on the solid supports and graft polymerized acrylic acid on top of the 1,2-pbd layers. This approach is the basis of the formation of an asymmetric membrane that requires different porosity on both of its sides.</AbstractText>
<CopyrightInformation>© 2011 American Chemical Society</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Hitrik</LastName>
<ForeName>Maria</ForeName>
<Initials>M</Initials>
<Affiliation>Institute of Chemistry, the Hebrew University of Jerusalem, Jerusalem 91904, Israel.</Affiliation>
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<ISSNLinking>0743-7463</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance>Butadienes</NameOfSubstance>
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<QualifierName MajorTopicYN="Y">chemistry</QualifierName>
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<QualifierName MajorTopicYN="Y">chemical synthesis</QualifierName>
<QualifierName MajorTopicYN="Y">chemistry</QualifierName>
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<QualifierName MajorTopicYN="N">chemistry</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="Y">Membranes, Artificial</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Particle Size</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N">Silicon</DescriptorName>
<QualifierName MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
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