Dispersion of single walled carbon nanotubes in organogels by incorporation into organogel fibers

Hybrid organogels were prepared, where single walled carbon nanotubes (SWNTs) were incorporated into organogel fibers. [Display omitted] ► Hybrid organogels bearing SWNTs mainly in gel fibers are prepared. ► Dispersion of SWNTs in organogels changes the gel properties. ► A gel-to-sol transition temp...

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Veröffentlicht in:Journal of colloid and interface science 2010-12, Vol.352 (1), p.121-127
Hauptverfasser: Oh, Hyukkeun, Jung, Byung Mun, Lee, Hyun Pyo, Chang, Ji Young
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creator Oh, Hyukkeun
Jung, Byung Mun
Lee, Hyun Pyo
Chang, Ji Young
description Hybrid organogels were prepared, where single walled carbon nanotubes (SWNTs) were incorporated into organogel fibers. [Display omitted] ► Hybrid organogels bearing SWNTs mainly in gel fibers are prepared. ► Dispersion of SWNTs in organogels changes the gel properties. ► A gel-to-sol transition temperature is influenced by a dispersion structure of SWNTs. We prepared hybrid organogels, where single walled carbon nanotubes (SWNTs) were incorporated into organogel fibers. The SWNTs were covalently functionalized with organic branches that had a similar structure to the organogelator. The effect of relative interactions between the carbon nanotubes (CNTs), organogelator, and solvent molecules on the hybrid organogel structure was investigated. Compounds 1 and 2 were synthesized from 3,4,5-tris(decyloxy)benzoic acid and 1,8-diaminooctane, as an organogelator and a functional group for SWNTs, respectively. Organogelator 1 showed excellent ability to gelate alkanes and alcohols. The pristine SWNTs were oxidized by acids to create carboxylic acid groups and functionalized covalently with compound 2 using thionyl chloride. Hybrid organogels of compound 1 with functionalized SWNTs (f-SWNTs) were prepared in decane and N,N-dimethylformamide (DMF). Transmission electron microscopy (TEM) images showed that the f-SWNTs in the hybrid organogel formed in decane were mainly located inside or on the surface of the organogel fibers, while the f-SWNTs in the hybrid organogel formed in DMF were distributed evenly over the sample. When an organogelator had a different chemical structure to that of an organic functional group on the SWNT surface, SWNTs existed as large aggregates, or long bundles, which were not incorporated inside of the organogel fibers.
doi_str_mv 10.1016/j.jcis.2010.08.025
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[Display omitted] ► Hybrid organogels bearing SWNTs mainly in gel fibers are prepared. ► Dispersion of SWNTs in organogels changes the gel properties. ► A gel-to-sol transition temperature is influenced by a dispersion structure of SWNTs. We prepared hybrid organogels, where single walled carbon nanotubes (SWNTs) were incorporated into organogel fibers. The SWNTs were covalently functionalized with organic branches that had a similar structure to the organogelator. The effect of relative interactions between the carbon nanotubes (CNTs), organogelator, and solvent molecules on the hybrid organogel structure was investigated. Compounds 1 and 2 were synthesized from 3,4,5-tris(decyloxy)benzoic acid and 1,8-diaminooctane, as an organogelator and a functional group for SWNTs, respectively. Organogelator 1 showed excellent ability to gelate alkanes and alcohols. 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[Display omitted] ► Hybrid organogels bearing SWNTs mainly in gel fibers are prepared. ► Dispersion of SWNTs in organogels changes the gel properties. ► A gel-to-sol transition temperature is influenced by a dispersion structure of SWNTs. We prepared hybrid organogels, where single walled carbon nanotubes (SWNTs) were incorporated into organogel fibers. The SWNTs were covalently functionalized with organic branches that had a similar structure to the organogelator. The effect of relative interactions between the carbon nanotubes (CNTs), organogelator, and solvent molecules on the hybrid organogel structure was investigated. Compounds 1 and 2 were synthesized from 3,4,5-tris(decyloxy)benzoic acid and 1,8-diaminooctane, as an organogelator and a functional group for SWNTs, respectively. Organogelator 1 showed excellent ability to gelate alkanes and alcohols. The pristine SWNTs were oxidized by acids to create carboxylic acid groups and functionalized covalently with compound 2 using thionyl chloride. Hybrid organogels of compound 1 with functionalized SWNTs (f-SWNTs) were prepared in decane and N,N-dimethylformamide (DMF). Transmission electron microscopy (TEM) images showed that the f-SWNTs in the hybrid organogel formed in decane were mainly located inside or on the surface of the organogel fibers, while the f-SWNTs in the hybrid organogel formed in DMF were distributed evenly over the sample. When an organogelator had a different chemical structure to that of an organic functional group on the SWNT surface, SWNTs existed as large aggregates, or long bundles, which were not incorporated inside of the organogel fibers.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>20817196</pmid><doi>10.1016/j.jcis.2010.08.025</doi><tpages>7</tpages></addata></record>
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subjects Benzoates - chemistry
Bundles
Carbon nanotube
Chemistry
Covalence
Diamines - chemistry
Dispersions
Exact sciences and technology
Fibers
Functional groups
Gels - chemical synthesis
Gels - chemistry
General and physical chemistry
Membranes, Artificial
Molecular Structure
Nanofiber
Nanotubes, Carbon - chemistry
Organogel
Particle Size
Self-assembly
Single wall carbon nanotubes
Surface Properties
Transmission electron microscopy
title Dispersion of single walled carbon nanotubes in organogels by incorporation into organogel fibers
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