Amphiphilic Cellulose Nanocrystals from Acid-Free Oxidative Treatment: Physicochemical Characteristics and Use as an Oil–Water Stabilizer

A chemical pretreatment for producing cellulose nanocrystals (CNCs) with periodate oxidation and reductive amination is reported. This new functionalization of cellulose fibers dispenses an alternative method for fabricating individual CNCs without the widely used acid hydrolysis process. CNCs can b...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biomacromolecules 2014-07, Vol.15 (7), p.2769-2775
Hauptverfasser: Visanko, Miikka, Liimatainen, Henrikki, Sirviö, Juho Antti, Heiskanen, Juha Pentti, Niinimäki, Jouko, Hormi, Osmo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2775
container_issue 7
container_start_page 2769
container_title Biomacromolecules
container_volume 15
creator Visanko, Miikka
Liimatainen, Henrikki
Sirviö, Juho Antti
Heiskanen, Juha Pentti
Niinimäki, Jouko
Hormi, Osmo
description A chemical pretreatment for producing cellulose nanocrystals (CNCs) with periodate oxidation and reductive amination is reported. This new functionalization of cellulose fibers dispenses an alternative method for fabricating individual CNCs without the widely used acid hydrolysis process. CNCs can be directly modified during the pretreatment step, and no additional post-treatments are required to tune the surface properties. Three butylamine isomers were tested to fabricate CNCs with amphiphilic features. After mechanical homogenization, CNCs occurred as individual crystallinities without aggregation where high uniformity in terms of shape and size was obtained. The elemental analysis and 1H NMR measurement show that iso- and n-butylamine attach the highest number of butylamino groups to the cellulose fibers. Linking the alkyl groups increases the hydrophobic nature of the CNCs, where water contact angles from self-standing films up to 110.5° are reported. Since these butylamino-functionalized CNCs have hydrophobic characteristics in addition to the hydrophilic backbone of cellulose, the stabilization impact on oil/water emulsions is demonstrated as a potential application.
doi_str_mv 10.1021/bm500628g
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1560120774</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1560120774</sourcerecordid><originalsourceid>FETCH-LOGICAL-a378t-10f86f7d2ed01cdad743e880fba7a546454300a43e3111894994cbdfec7a8a203</originalsourceid><addsrcrecordid>eNqFkc9u1DAQxi0EoqVw4AWQL0jlkDJ2nDjhtlrRUqlikWjFMZrYE9ZV_iy2g1hO3Dn2DXmSuu3SXpCQRpqR_dP3aeZj7KWAIwFSvG2HAqCU1ddHbF8UssxUCfLx7VxkWtd6jz0L4RIA6lwVT9meVHVCoNxnvxfDZu1S9c7wJfX93E-B-EccJ-O3IWIfeOengS-Ms9mxJ-KrH85idN-Jn3vCONAY3_FP621wZjJrGpzBni_X6NFE8i5EZwLH0fKLJIw3I1-5_s-vqy-Y_vnniG1y_0n-OXvSJT96sesH7OL4_fnyQ3a2OjldLs4yzHUVMwFdVXbaSrIgjEWrVU5VBV2LGgtVqkLlAJgecyFEVau6Vqa1HRmNFUrID9jhne7GT99mCrEZXDBpdxxpmkMjihKEBJ10_4-qIlnkMk_omzvU-CkET12z8W5Av20ENDcxNfcxJfbVTnZuB7L35N9cEvB6B2BI5-w8jsaFB64q67QbPHBoQnM5zX5Mh_uH4TXJOqgh</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1545189323</pqid></control><display><type>article</type><title>Amphiphilic Cellulose Nanocrystals from Acid-Free Oxidative Treatment: Physicochemical Characteristics and Use as an Oil–Water Stabilizer</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Visanko, Miikka ; Liimatainen, Henrikki ; Sirviö, Juho Antti ; Heiskanen, Juha Pentti ; Niinimäki, Jouko ; Hormi, Osmo</creator><creatorcontrib>Visanko, Miikka ; Liimatainen, Henrikki ; Sirviö, Juho Antti ; Heiskanen, Juha Pentti ; Niinimäki, Jouko ; Hormi, Osmo</creatorcontrib><description>A chemical pretreatment for producing cellulose nanocrystals (CNCs) with periodate oxidation and reductive amination is reported. This new functionalization of cellulose fibers dispenses an alternative method for fabricating individual CNCs without the widely used acid hydrolysis process. CNCs can be directly modified during the pretreatment step, and no additional post-treatments are required to tune the surface properties. Three butylamine isomers were tested to fabricate CNCs with amphiphilic features. After mechanical homogenization, CNCs occurred as individual crystallinities without aggregation where high uniformity in terms of shape and size was obtained. The elemental analysis and 1H NMR measurement show that iso- and n-butylamine attach the highest number of butylamino groups to the cellulose fibers. Linking the alkyl groups increases the hydrophobic nature of the CNCs, where water contact angles from self-standing films up to 110.5° are reported. Since these butylamino-functionalized CNCs have hydrophobic characteristics in addition to the hydrophilic backbone of cellulose, the stabilization impact on oil/water emulsions is demonstrated as a potential application.</description><identifier>ISSN: 1525-7797</identifier><identifier>EISSN: 1526-4602</identifier><identifier>DOI: 10.1021/bm500628g</identifier><identifier>PMID: 24946006</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Butylamines - chemistry ; Cellulose - chemistry ; Cellulose and derivatives ; Crystallography, X-Ray ; Emulsions ; Exact sciences and technology ; Hydrophobic and Hydrophilic Interactions ; Nanoparticles - chemistry ; Natural polymers ; Oxidation-Reduction ; Physicochemistry of polymers ; Soybean Oil - chemistry ; Surface-Active Agents - chemistry ; Viscosity ; Water - chemistry</subject><ispartof>Biomacromolecules, 2014-07, Vol.15 (7), p.2769-2775</ispartof><rights>Copyright © 2014 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a378t-10f86f7d2ed01cdad743e880fba7a546454300a43e3111894994cbdfec7a8a203</citedby><cites>FETCH-LOGICAL-a378t-10f86f7d2ed01cdad743e880fba7a546454300a43e3111894994cbdfec7a8a203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/bm500628g$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bm500628g$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28691110$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24946006$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Visanko, Miikka</creatorcontrib><creatorcontrib>Liimatainen, Henrikki</creatorcontrib><creatorcontrib>Sirviö, Juho Antti</creatorcontrib><creatorcontrib>Heiskanen, Juha Pentti</creatorcontrib><creatorcontrib>Niinimäki, Jouko</creatorcontrib><creatorcontrib>Hormi, Osmo</creatorcontrib><title>Amphiphilic Cellulose Nanocrystals from Acid-Free Oxidative Treatment: Physicochemical Characteristics and Use as an Oil–Water Stabilizer</title><title>Biomacromolecules</title><addtitle>Biomacromolecules</addtitle><description>A chemical pretreatment for producing cellulose nanocrystals (CNCs) with periodate oxidation and reductive amination is reported. This new functionalization of cellulose fibers dispenses an alternative method for fabricating individual CNCs without the widely used acid hydrolysis process. CNCs can be directly modified during the pretreatment step, and no additional post-treatments are required to tune the surface properties. Three butylamine isomers were tested to fabricate CNCs with amphiphilic features. After mechanical homogenization, CNCs occurred as individual crystallinities without aggregation where high uniformity in terms of shape and size was obtained. The elemental analysis and 1H NMR measurement show that iso- and n-butylamine attach the highest number of butylamino groups to the cellulose fibers. Linking the alkyl groups increases the hydrophobic nature of the CNCs, where water contact angles from self-standing films up to 110.5° are reported. Since these butylamino-functionalized CNCs have hydrophobic characteristics in addition to the hydrophilic backbone of cellulose, the stabilization impact on oil/water emulsions is demonstrated as a potential application.</description><subject>Applied sciences</subject><subject>Butylamines - chemistry</subject><subject>Cellulose - chemistry</subject><subject>Cellulose and derivatives</subject><subject>Crystallography, X-Ray</subject><subject>Emulsions</subject><subject>Exact sciences and technology</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Nanoparticles - chemistry</subject><subject>Natural polymers</subject><subject>Oxidation-Reduction</subject><subject>Physicochemistry of polymers</subject><subject>Soybean Oil - chemistry</subject><subject>Surface-Active Agents - chemistry</subject><subject>Viscosity</subject><subject>Water - chemistry</subject><issn>1525-7797</issn><issn>1526-4602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQxi0EoqVw4AWQL0jlkDJ2nDjhtlrRUqlikWjFMZrYE9ZV_iy2g1hO3Dn2DXmSuu3SXpCQRpqR_dP3aeZj7KWAIwFSvG2HAqCU1ddHbF8UssxUCfLx7VxkWtd6jz0L4RIA6lwVT9meVHVCoNxnvxfDZu1S9c7wJfX93E-B-EccJ-O3IWIfeOengS-Ms9mxJ-KrH85idN-Jn3vCONAY3_FP621wZjJrGpzBni_X6NFE8i5EZwLH0fKLJIw3I1-5_s-vqy-Y_vnniG1y_0n-OXvSJT96sesH7OL4_fnyQ3a2OjldLs4yzHUVMwFdVXbaSrIgjEWrVU5VBV2LGgtVqkLlAJgecyFEVau6Vqa1HRmNFUrID9jhne7GT99mCrEZXDBpdxxpmkMjihKEBJ10_4-qIlnkMk_omzvU-CkET12z8W5Av20ENDcxNfcxJfbVTnZuB7L35N9cEvB6B2BI5-w8jsaFB64q67QbPHBoQnM5zX5Mh_uH4TXJOqgh</recordid><startdate>20140714</startdate><enddate>20140714</enddate><creator>Visanko, Miikka</creator><creator>Liimatainen, Henrikki</creator><creator>Sirviö, Juho Antti</creator><creator>Heiskanen, Juha Pentti</creator><creator>Niinimäki, Jouko</creator><creator>Hormi, Osmo</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></search><sort><creationdate>20140714</creationdate><title>Amphiphilic Cellulose Nanocrystals from Acid-Free Oxidative Treatment: Physicochemical Characteristics and Use as an Oil–Water Stabilizer</title><author>Visanko, Miikka ; Liimatainen, Henrikki ; Sirviö, Juho Antti ; Heiskanen, Juha Pentti ; Niinimäki, Jouko ; Hormi, Osmo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a378t-10f86f7d2ed01cdad743e880fba7a546454300a43e3111894994cbdfec7a8a203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Applied sciences</topic><topic>Butylamines - chemistry</topic><topic>Cellulose - chemistry</topic><topic>Cellulose and derivatives</topic><topic>Crystallography, X-Ray</topic><topic>Emulsions</topic><topic>Exact sciences and technology</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Nanoparticles - chemistry</topic><topic>Natural polymers</topic><topic>Oxidation-Reduction</topic><topic>Physicochemistry of polymers</topic><topic>Soybean Oil - chemistry</topic><topic>Surface-Active Agents - chemistry</topic><topic>Viscosity</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Visanko, Miikka</creatorcontrib><creatorcontrib>Liimatainen, Henrikki</creatorcontrib><creatorcontrib>Sirviö, Juho Antti</creatorcontrib><creatorcontrib>Heiskanen, Juha Pentti</creatorcontrib><creatorcontrib>Niinimäki, Jouko</creatorcontrib><creatorcontrib>Hormi, Osmo</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><jtitle>Biomacromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Visanko, Miikka</au><au>Liimatainen, Henrikki</au><au>Sirviö, Juho Antti</au><au>Heiskanen, Juha Pentti</au><au>Niinimäki, Jouko</au><au>Hormi, Osmo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amphiphilic Cellulose Nanocrystals from Acid-Free Oxidative Treatment: Physicochemical Characteristics and Use as an Oil–Water Stabilizer</atitle><jtitle>Biomacromolecules</jtitle><addtitle>Biomacromolecules</addtitle><date>2014-07-14</date><risdate>2014</risdate><volume>15</volume><issue>7</issue><spage>2769</spage><epage>2775</epage><pages>2769-2775</pages><issn>1525-7797</issn><eissn>1526-4602</eissn><abstract>A chemical pretreatment for producing cellulose nanocrystals (CNCs) with periodate oxidation and reductive amination is reported. This new functionalization of cellulose fibers dispenses an alternative method for fabricating individual CNCs without the widely used acid hydrolysis process. CNCs can be directly modified during the pretreatment step, and no additional post-treatments are required to tune the surface properties. Three butylamine isomers were tested to fabricate CNCs with amphiphilic features. After mechanical homogenization, CNCs occurred as individual crystallinities without aggregation where high uniformity in terms of shape and size was obtained. The elemental analysis and 1H NMR measurement show that iso- and n-butylamine attach the highest number of butylamino groups to the cellulose fibers. Linking the alkyl groups increases the hydrophobic nature of the CNCs, where water contact angles from self-standing films up to 110.5° are reported. Since these butylamino-functionalized CNCs have hydrophobic characteristics in addition to the hydrophilic backbone of cellulose, the stabilization impact on oil/water emulsions is demonstrated as a potential application.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>24946006</pmid><doi>10.1021/bm500628g</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1525-7797
ispartof Biomacromolecules, 2014-07, Vol.15 (7), p.2769-2775
issn 1525-7797
1526-4602
language eng
recordid cdi_proquest_miscellaneous_1560120774
source MEDLINE; American Chemical Society Journals
subjects Applied sciences
Butylamines - chemistry
Cellulose - chemistry
Cellulose and derivatives
Crystallography, X-Ray
Emulsions
Exact sciences and technology
Hydrophobic and Hydrophilic Interactions
Nanoparticles - chemistry
Natural polymers
Oxidation-Reduction
Physicochemistry of polymers
Soybean Oil - chemistry
Surface-Active Agents - chemistry
Viscosity
Water - chemistry
title Amphiphilic Cellulose Nanocrystals from Acid-Free Oxidative Treatment: Physicochemical Characteristics and Use as an Oil–Water Stabilizer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T03%3A39%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Amphiphilic%20Cellulose%20Nanocrystals%20from%20Acid-Free%20Oxidative%20Treatment:%20Physicochemical%20Characteristics%20and%20Use%20as%20an%20Oil%E2%80%93Water%20Stabilizer&rft.jtitle=Biomacromolecules&rft.au=Visanko,%20Miikka&rft.date=2014-07-14&rft.volume=15&rft.issue=7&rft.spage=2769&rft.epage=2775&rft.pages=2769-2775&rft.issn=1525-7797&rft.eissn=1526-4602&rft_id=info:doi/10.1021/bm500628g&rft_dat=%3Cproquest_cross%3E1560120774%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1545189323&rft_id=info:pmid/24946006&rfr_iscdi=true