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Pressure Cell Assisted Solution Characterization of Polysaccharides. 1. Guar Gum
To reduce time-dependent aggregation phenomena and achieve true “molecular” solution, the “pressure cell” solubilization method of Vorwerg and co-workers was applied to solutions of guar galactomannans (three samples of different molecular weights), using various heating, time, and pressure profiles...
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Published in: | Biomacromolecules 2001, Vol.2 (4), p.1301-1309 |
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description | To reduce time-dependent aggregation phenomena and achieve true “molecular” solution, the “pressure cell” solubilization method of Vorwerg and co-workers was applied to solutions of guar galactomannans (three samples of different molecular weights), using various heating, time, and pressure profiles. Physicochemical characterization of the guar samples before and after pressure cell treatment included measurements of intrinsic viscosity [η] by capillary viscometry and M w and radius of gyration from size exclusion chromatography coupled to multiangle laser light scattering (SEC/MALLS). Heating the guar solutions (100−160 °C) without pressurization produced chain degradation with [η] and M w values being reduced significantly, whereas this effect was reduced substantially for samples subject to initial pressurization (∼5−10 bar). The constants in the Mark−Houwink−Sakurada equation, relating [η] and M w were established and the characteristic ratio C ∞ and chain persistence length L p were calculated using both the Burchard−Stockmayer−Fixman (BSF) method for flexible and semiflexible chains and the Hearst method more appropriate for stiffened chains. Definitive conclusions can now be drawn on the flexibility of the guar chain backbone, with L p ≈ 4 nm from the BSF plot, in good agreement with previously published work using such geometric methods. This contrasts with the higher values obtained from extrapolation of data for polyelectrolytes with a similar backbone geometry, such as sodium carboxymethyl cellulose, to “infinite” ionic strength. |
doi_str_mv | 10.1021/bm010118n |
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Guar Gum</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Picout, David R ; Ross-Murphy, Simon B ; Errington, Neil ; Harding, Stephen E</creator><creatorcontrib>Picout, David R ; Ross-Murphy, Simon B ; Errington, Neil ; Harding, Stephen E</creatorcontrib><description>To reduce time-dependent aggregation phenomena and achieve true “molecular” solution, the “pressure cell” solubilization method of Vorwerg and co-workers was applied to solutions of guar galactomannans (three samples of different molecular weights), using various heating, time, and pressure profiles. Physicochemical characterization of the guar samples before and after pressure cell treatment included measurements of intrinsic viscosity [η] by capillary viscometry and M w and radius of gyration from size exclusion chromatography coupled to multiangle laser light scattering (SEC/MALLS). Heating the guar solutions (100−160 °C) without pressurization produced chain degradation with [η] and M w values being reduced significantly, whereas this effect was reduced substantially for samples subject to initial pressurization (∼5−10 bar). The constants in the Mark−Houwink−Sakurada equation, relating [η] and M w were established and the characteristic ratio C ∞ and chain persistence length L p were calculated using both the Burchard−Stockmayer−Fixman (BSF) method for flexible and semiflexible chains and the Hearst method more appropriate for stiffened chains. Definitive conclusions can now be drawn on the flexibility of the guar chain backbone, with L p ≈ 4 nm from the BSF plot, in good agreement with previously published work using such geometric methods. 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Guar Gum</title><title>Biomacromolecules</title><addtitle>Biomacromolecules</addtitle><description>To reduce time-dependent aggregation phenomena and achieve true “molecular” solution, the “pressure cell” solubilization method of Vorwerg and co-workers was applied to solutions of guar galactomannans (three samples of different molecular weights), using various heating, time, and pressure profiles. Physicochemical characterization of the guar samples before and after pressure cell treatment included measurements of intrinsic viscosity [η] by capillary viscometry and M w and radius of gyration from size exclusion chromatography coupled to multiangle laser light scattering (SEC/MALLS). Heating the guar solutions (100−160 °C) without pressurization produced chain degradation with [η] and M w values being reduced significantly, whereas this effect was reduced substantially for samples subject to initial pressurization (∼5−10 bar). The constants in the Mark−Houwink−Sakurada equation, relating [η] and M w were established and the characteristic ratio C ∞ and chain persistence length L p were calculated using both the Burchard−Stockmayer−Fixman (BSF) method for flexible and semiflexible chains and the Hearst method more appropriate for stiffened chains. Definitive conclusions can now be drawn on the flexibility of the guar chain backbone, with L p ≈ 4 nm from the BSF plot, in good agreement with previously published work using such geometric methods. This contrasts with the higher values obtained from extrapolation of data for polyelectrolytes with a similar backbone geometry, such as sodium carboxymethyl cellulose, to “infinite” ionic strength.</description><subject>Carbohydrate Conformation</subject><subject>Galactans - analysis</subject><subject>Galactans - chemistry</subject><subject>Mannans - analysis</subject><subject>Mannans - chemistry</subject><subject>Plant Gums</subject><subject>Pliability</subject><subject>Pressure</subject><subject>Temperature</subject><subject>Viscosity</subject><issn>1525-7797</issn><issn>1526-4602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp9kE1Lw0AQhhdRrFYP_gHJRcVD6s5-ZNNjCVqFggV7D5v9wJQkW3eTQ_31rm3Ri3iZGWYeXpgHoSvAE8AEHqoWAwbIuyN0BpxkKcswOd7NPBViKkboPIQ1xnhKGT9FIwAhBMPiDC2X3oQweJMUpmmSWQh16I1O3lwz9LXrkuJdeql64-tPuVs4myxdsw1SqXiqtQmTBCbJfJA-lvYCnVjZBHN56GO0enpcFc_p4nX-UswWqaSM9mllecUAV4QqiD8QynOirNZSa5Exm3GKZZ6JTDMmiK14BkTk1FicY-Ca0TG628duvPsYTOjLtg4qviA744ZQCs44Ewwgkrf_k4TmHKbTCN7vQeVdCN7YcuPrVvptCbj89lz-eI7s9SF0qFqjf8mD2Ajc7AGpQrl2g--ijD-CvgALz4JT</recordid><startdate>2001</startdate><enddate>2001</enddate><creator>Picout, David R</creator><creator>Ross-Murphy, Simon B</creator><creator>Errington, Neil</creator><creator>Harding, Stephen E</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>2001</creationdate><title>Pressure Cell Assisted Solution Characterization of Polysaccharides. 1. 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Guar Gum</atitle><jtitle>Biomacromolecules</jtitle><addtitle>Biomacromolecules</addtitle><date>2001</date><risdate>2001</risdate><volume>2</volume><issue>4</issue><spage>1301</spage><epage>1309</epage><pages>1301-1309</pages><issn>1525-7797</issn><eissn>1526-4602</eissn><abstract>To reduce time-dependent aggregation phenomena and achieve true “molecular” solution, the “pressure cell” solubilization method of Vorwerg and co-workers was applied to solutions of guar galactomannans (three samples of different molecular weights), using various heating, time, and pressure profiles. Physicochemical characterization of the guar samples before and after pressure cell treatment included measurements of intrinsic viscosity [η] by capillary viscometry and M w and radius of gyration from size exclusion chromatography coupled to multiangle laser light scattering (SEC/MALLS). Heating the guar solutions (100−160 °C) without pressurization produced chain degradation with [η] and M w values being reduced significantly, whereas this effect was reduced substantially for samples subject to initial pressurization (∼5−10 bar). The constants in the Mark−Houwink−Sakurada equation, relating [η] and M w were established and the characteristic ratio C ∞ and chain persistence length L p were calculated using both the Burchard−Stockmayer−Fixman (BSF) method for flexible and semiflexible chains and the Hearst method more appropriate for stiffened chains. Definitive conclusions can now be drawn on the flexibility of the guar chain backbone, with L p ≈ 4 nm from the BSF plot, in good agreement with previously published work using such geometric methods. This contrasts with the higher values obtained from extrapolation of data for polyelectrolytes with a similar backbone geometry, such as sodium carboxymethyl cellulose, to “infinite” ionic strength.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>11777407</pmid><doi>10.1021/bm010118n</doi><tpages>9</tpages></addata></record> |
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subjects | Carbohydrate Conformation Galactans - analysis Galactans - chemistry Mannans - analysis Mannans - chemistry Plant Gums Pliability Pressure Temperature Viscosity |
title | Pressure Cell Assisted Solution Characterization of Polysaccharides. 1. Guar Gum |
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