Amorphous Characteristics of an Ultrathin Cellulose Film
Swelling behavior and rearrangements of an amorphous ultrathin cellulose film (20 nm thickness) exposed to water and subsequently dried were investigated with grazing incidence X-ray diffraction, neutron reflectivity, atomic force microscopy, and surface energy calculations obtained from contact ang...
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Veröffentlicht in: | Biomacromolecules 2011-03, Vol.12 (3), p.770-777 |
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creator | Kontturi, Eero Suchy, Miro Penttilä, Paavo Jean, Bruno Pirkkalainen, Kari Torkkeli, Mika Serimaa, Ritva |
description | Swelling behavior and rearrangements of an amorphous ultrathin cellulose film (20 nm thickness) exposed to water and subsequently dried were investigated with grazing incidence X-ray diffraction, neutron reflectivity, atomic force microscopy, and surface energy calculations obtained from contact angle measurements. The film swelled excessively in water, doubling its thickness, but shrunk back to the original thickness upon water removal. Crystallinity (or amorphousness) and morphology remained relatively unchanged after the wetting/drying cycle, but surface free energy increased considerably (ca. 15%) due to an increase in its polar component, that is, the hydrophilicity of the film, indicating that rearrangements occurred during the film’s exposure to water. Furthermore, stability of the films in aqueous NaOH solution was investigated with quartz crystal microbalance with dissipation monitoring. The films were stable at 0.0001 M NaOH but already 0.001 M NaOH partially dissolved the film. The surprising susceptibility to dissolve in dilute NaOH was hypothetically attributed to the lack of hierarchical morphology in the amorphous film. |
doi_str_mv | 10.1021/bm101382q |
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The film swelled excessively in water, doubling its thickness, but shrunk back to the original thickness upon water removal. Crystallinity (or amorphousness) and morphology remained relatively unchanged after the wetting/drying cycle, but surface free energy increased considerably (ca. 15%) due to an increase in its polar component, that is, the hydrophilicity of the film, indicating that rearrangements occurred during the film’s exposure to water. Furthermore, stability of the films in aqueous NaOH solution was investigated with quartz crystal microbalance with dissipation monitoring. The films were stable at 0.0001 M NaOH but already 0.001 M NaOH partially dissolved the film. 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The film swelled excessively in water, doubling its thickness, but shrunk back to the original thickness upon water removal. Crystallinity (or amorphousness) and morphology remained relatively unchanged after the wetting/drying cycle, but surface free energy increased considerably (ca. 15%) due to an increase in its polar component, that is, the hydrophilicity of the film, indicating that rearrangements occurred during the film’s exposure to water. Furthermore, stability of the films in aqueous NaOH solution was investigated with quartz crystal microbalance with dissipation monitoring. The films were stable at 0.0001 M NaOH but already 0.001 M NaOH partially dissolved the film. The surprising susceptibility to dissolve in dilute NaOH was hypothetically attributed to the lack of hierarchical morphology in the amorphous film.</description><subject>Absorption</subject><subject>Applied sciences</subject><subject>Cellulose - chemistry</subject><subject>Cellulose and derivatives</subject><subject>Chemistry Techniques, Analytical</subject><subject>Exact sciences and technology</subject><subject>Molecular Conformation</subject><subject>Natural polymers</subject><subject>Physicochemistry of polymers</subject><subject>Sodium Hydroxide</subject><subject>Solubility</subject><subject>Water - chemistry</subject><issn>1525-7797</issn><issn>1526-4602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLw0AUhQdRbK0u_AOSjYiL6J13sizBWqHgxq6HyWSGpuTRziSC_97U1nYjuLqXy8e55xyEbjE8YSD4Oa8xYJqQ7RkaY05EzASQ85-dx1KmcoSuQlgDQEoZv0QjgknKOOdjlEzr1m9WbR-ibKW9Np31ZehKE6LWRbqJllXndbcqmyizVdVXbbDRrKzqa3ThdBXszWFO0HL28pHN48X761s2XcSaSdHFOXEJA5ZbbrGVtDCycJrnAmTCE0GlBJdQnErIwWFWFFIUhROSSTDO2JzSCXrc6650pTa-rLX_Uq0u1Xy6ULsbgAAKkn_igX3YsxvfbnsbOlWXwQy2dWOHhCrFGAuRkP_JwRqjhDB--m98G4K37mgCg9q1r47tD-zdQbXPa1scyd-6B-D-AOhgdOW8bkwZThxNBRnynDhtglq3vW-Giv94-A18tJXV</recordid><startdate>20110314</startdate><enddate>20110314</enddate><creator>Kontturi, Eero</creator><creator>Suchy, Miro</creator><creator>Penttilä, Paavo</creator><creator>Jean, Bruno</creator><creator>Pirkkalainen, Kari</creator><creator>Torkkeli, Mika</creator><creator>Serimaa, Ritva</creator><general>American Chemical Society</general><scope>IQODW</scope><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><scope>1XC</scope></search><sort><creationdate>20110314</creationdate><title>Amorphous Characteristics of an Ultrathin Cellulose Film</title><author>Kontturi, Eero ; Suchy, Miro ; Penttilä, Paavo ; Jean, Bruno ; Pirkkalainen, Kari ; Torkkeli, Mika ; Serimaa, Ritva</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a476t-b2f8404be5e1e73dc7dfa5b60785863770f831970b0f14dd76ddf67470cfceb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Absorption</topic><topic>Applied sciences</topic><topic>Cellulose - chemistry</topic><topic>Cellulose and derivatives</topic><topic>Chemistry Techniques, Analytical</topic><topic>Exact sciences and technology</topic><topic>Molecular Conformation</topic><topic>Natural polymers</topic><topic>Physicochemistry of polymers</topic><topic>Sodium Hydroxide</topic><topic>Solubility</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kontturi, Eero</creatorcontrib><creatorcontrib>Suchy, Miro</creatorcontrib><creatorcontrib>Penttilä, Paavo</creatorcontrib><creatorcontrib>Jean, Bruno</creatorcontrib><creatorcontrib>Pirkkalainen, Kari</creatorcontrib><creatorcontrib>Torkkeli, Mika</creatorcontrib><creatorcontrib>Serimaa, Ritva</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Biomacromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kontturi, Eero</au><au>Suchy, Miro</au><au>Penttilä, Paavo</au><au>Jean, Bruno</au><au>Pirkkalainen, Kari</au><au>Torkkeli, Mika</au><au>Serimaa, Ritva</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amorphous Characteristics of an Ultrathin Cellulose Film</atitle><jtitle>Biomacromolecules</jtitle><addtitle>Biomacromolecules</addtitle><date>2011-03-14</date><risdate>2011</risdate><volume>12</volume><issue>3</issue><spage>770</spage><epage>777</epage><pages>770-777</pages><issn>1525-7797</issn><eissn>1526-4602</eissn><abstract>Swelling behavior and rearrangements of an amorphous ultrathin cellulose film (20 nm thickness) exposed to water and subsequently dried were investigated with grazing incidence X-ray diffraction, neutron reflectivity, atomic force microscopy, and surface energy calculations obtained from contact angle measurements. The film swelled excessively in water, doubling its thickness, but shrunk back to the original thickness upon water removal. Crystallinity (or amorphousness) and morphology remained relatively unchanged after the wetting/drying cycle, but surface free energy increased considerably (ca. 15%) due to an increase in its polar component, that is, the hydrophilicity of the film, indicating that rearrangements occurred during the film’s exposure to water. Furthermore, stability of the films in aqueous NaOH solution was investigated with quartz crystal microbalance with dissipation monitoring. The films were stable at 0.0001 M NaOH but already 0.001 M NaOH partially dissolved the film. The surprising susceptibility to dissolve in dilute NaOH was hypothetically attributed to the lack of hierarchical morphology in the amorphous film.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>21294555</pmid><doi>10.1021/bm101382q</doi><tpages>8</tpages></addata></record> |
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subjects | Absorption Applied sciences Cellulose - chemistry Cellulose and derivatives Chemistry Techniques, Analytical Exact sciences and technology Molecular Conformation Natural polymers Physicochemistry of polymers Sodium Hydroxide Solubility Water - chemistry |
title | Amorphous Characteristics of an Ultrathin Cellulose Film |
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