TY - JOUR
T1 - Interfacial Hydrolysis of Acetals on Protonated TEMPO-oxidized Cellulose Nanofibers
AU - Tamura, Yuya
AU - Kanomata, Kyohei
AU - Kitaoka, Takuya
N1 - Funding Information:
This research was supported by an Advanced Low Carbon Technology Research and Development Program from the Japan Science and Technology Agency (T.K.), a Grant-in-Aid for Challenging Exploratory Research (16K14959) from the Ministry of Education, Culture, Sports, Science, and Technology, Japan (T.K.), and a Research Fellowship for Young Scientists from the Japan Society for the Promotion of Science (K.K.). The authors gratefully thank Prof. Dr. Syuntaro Hiradate and Prof. Dr. Yuki Mori for performing XRD analysis. The authors also thank Ms. Kana Ichibakase for technical support.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - 2,2,6,6-Tetramethylpiperidine-1-oxyl (TEMPO)-oxidized cellulose nanofibers (TOCNs), which have a high-density of exposed carboxylic acid groups on their crystalline surfaces, effectively act as acid catalysts in acetal hydrolysis. Carboxy-free cellulose nanofibers, polymeric carboxylic acids, and homogeneous acetic acid do not show significant catalytic activity under the same reaction conditions. Mercerized TOCNs differing from the original TOCNs in a crystalline structure were also ineffective, which suggests that the unique nanoarchitectural features of TOCNs, such as regularly aligned carboxylic acid groups, large specific surface areas, and structural rigidity, must be major factors in the acceleration of acetal hydrolysis. Kinetic analysis suggested that substrates and/or acid catalyst species were concentrated on the TOCN crystalline surfaces, which significantly enhanced the catalytic activity.
AB - 2,2,6,6-Tetramethylpiperidine-1-oxyl (TEMPO)-oxidized cellulose nanofibers (TOCNs), which have a high-density of exposed carboxylic acid groups on their crystalline surfaces, effectively act as acid catalysts in acetal hydrolysis. Carboxy-free cellulose nanofibers, polymeric carboxylic acids, and homogeneous acetic acid do not show significant catalytic activity under the same reaction conditions. Mercerized TOCNs differing from the original TOCNs in a crystalline structure were also ineffective, which suggests that the unique nanoarchitectural features of TOCNs, such as regularly aligned carboxylic acid groups, large specific surface areas, and structural rigidity, must be major factors in the acceleration of acetal hydrolysis. Kinetic analysis suggested that substrates and/or acid catalyst species were concentrated on the TOCN crystalline surfaces, which significantly enhanced the catalytic activity.
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U2 - 10.1038/s41598-018-23381-8
DO - 10.1038/s41598-018-23381-8
M3 - Article
C2 - 29568037
AN - SCOPUS:85044300568
SN - 2045-2322
VL - 8
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 5021
ER -