dc.contributor |
Aalto-yliopisto |
fi |
dc.contributor |
Aalto University |
en |
dc.contributor.author |
Borrega, Marc |
|
dc.contributor.author |
Larsson, Per Tomas |
|
dc.contributor.author |
Ahvenainen, Patrik |
|
dc.contributor.author |
Ceccherini, Sara |
|
dc.contributor.author |
Maloney, Thaddeus |
|
dc.contributor.author |
Rautkari, Lauri |
|
dc.contributor.author |
Sixta, Herbert |
|
dc.date.accessioned |
2018-05-22T14:52:26Z |
|
dc.date.available |
2018-05-22T14:52:26Z |
|
dc.date.issued |
2018-06-15 |
|
dc.identifier.citation |
Borrega , M , Larsson , P T , Ahvenainen , P , Ceccherini , S , Maloney , T , Rautkari , L & Sixta , H 2018 , ' Birch wood pre-hydrolysis vs pulp post-hydrolysis for the production of xylan-based compounds and cellulose for viscose application ' Carbohydrate Polymers , vol 190 , pp. 212-221 . DOI: 10.1016/j.carbpol.2018.02.064 |
en |
dc.identifier.issn |
0144-8617 |
|
dc.identifier.issn |
1879-1344 |
|
dc.identifier.other |
PURE UUID: f0524855-3cf7-428b-afe0-e852f6eda7c3 |
|
dc.identifier.other |
PURE ITEMURL: https://research.aalto.fi/en/publications/birch-wood-prehydrolysis-vs-pulp-posthydrolysis-for-the-production-of-xylanbased-compounds-and-cellulose-for-viscose-application(f0524855-3cf7-428b-afe0-e852f6eda7c3).html |
|
dc.identifier.other |
PURE LINK: http://www.scopus.com/inward/record.url?scp=85042777891&partnerID=8YFLogxK |
|
dc.identifier.other |
PURE FILEURL: https://research.aalto.fi/files/20722606/Borrega_et_al_Birch_wood_2018_Carbohydrate_Polymers.pdf |
|
dc.identifier.uri |
https://aaltodoc.aalto.fi/handle/123456789/31255 |
|
dc.description.abstract |
Hydrothermal treatments of birch wood and kraft pulp were compared for their ability to extract the xylan and produce viscose-grade pulp. Water post-hydrolysis of kraft pulp produced a high-purity cellulosic pulp with lower viscosity but higher cellulose yield than traditional pre-hydrolysis kraft pulping of wood. Post-hydrolysis of pulp also increased the crystallite dimensions and degree of crystallinity in cellulose, and promoted a higher extent of fibril aggregation. The lower specific surface area in post-hydrolyzed pulps, derived from their larger fibril aggregates, decreased the accessibility of –OH groups. However, this lower accessibility did not seem to decrease the pulp reactivity to derivatizing chemicals. In the aqueous side-stream, the xylose yield was similar in both pre- and post-hydrolysates, although conducting post-hydrolysis of pulp in a flow-through system enabled the recovery of high purity and molar mass (∼10 kDa) xylan for high-value applications. |
en |
dc.format.extent |
10 |
|
dc.format.extent |
212-221 |
|
dc.format.mimetype |
application/pdf |
|
dc.language.iso |
en |
en |
dc.relation.ispartofseries |
Carbohydrate Polymers |
en |
dc.relation.ispartofseries |
Volume 190 |
en |
dc.rights |
openAccess |
en |
dc.subject.other |
Organic Chemistry |
en |
dc.subject.other |
Polymers and Plastics |
en |
dc.subject.other |
Materials Chemistry |
en |
dc.subject.other |
216 Materials engineering |
en |
dc.title |
Birch wood pre-hydrolysis vs pulp post-hydrolysis for the production of xylan-based compounds and cellulose for viscose application |
en |
dc.type |
A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä |
fi |
dc.description.version |
Peer reviewed |
en |
dc.contributor.department |
Department of Forest Products Technology |
|
dc.contributor.department |
RISE Bioeconomy |
|
dc.contributor.department |
University of Helsinki |
|
dc.contributor.department |
Department of Bioproducts and Biosystems |
|
dc.subject.keyword |
Cellulose |
|
dc.subject.keyword |
Dissolving pulp |
|
dc.subject.keyword |
Hydrothermal treatment |
|
dc.subject.keyword |
Viscose |
|
dc.subject.keyword |
Xylan |
|
dc.subject.keyword |
Organic Chemistry |
|
dc.subject.keyword |
Polymers and Plastics |
|
dc.subject.keyword |
Materials Chemistry |
|
dc.subject.keyword |
216 Materials engineering |
|
dc.identifier.urn |
URN:NBN:fi:aalto-201805222695 |
|
dc.identifier.doi |
10.1016/j.carbpol.2018.02.064 |
|
dc.date.embargo |
info:eu-repo/date/embargoEnd/2019-02-25 |
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