From cellulose fibrils to single chains: understanding cellulose dissolution in ionic liquids

Literature Information

Publication Date 2015-11-05
DOI 10.1039/C5CP05744B
Impact Factor 3.676
Authors

Xueming Yuan, Gang Cheng


View Original

Abstract

Cellulose is the most abundant and renewable organic compound on Earth, it is however not soluble in common organic solvents and aqueous solutions. Cellulose dissolution is a key aspect to promote its value-added applications. Ionic liquids (ILs) have been shown to solubilize cellulose under relatively mild conditions. The easy processability of cellulose with ILs and their environmental-friendly nature prompted research in various fields such as biomass pretreatment and conversion, cellulose fiber and composite production, and chemical conversion of cellulose in ILs. Progress has been made on understanding the mechanism of cellulose dissolution in ILs, including the structural characteristics of ILs that are cellulose solvents, however many details remain unknown. In light of rapid development and importance of cellulose dissolution in the field of IL-based cellulose and biomass processing, it is necessary to provide an overview of current understanding of cellulose dissolution in ILs and outline possible future research trends. Recent literature studies suggest that synergistic effects between the anions and the cations of ILs need to be revealed, which requires refining the structure of cellulose elementary fibrils, simulation of more realistic cellulose fibrils and detailed studies on the solution structure of cellulose in ILs. After analyzing literature studies, three interacting modules are identified, which are crucial to understand the process of cellulose dissolution in ILs: (1) the structure of elementary fibrils; (2) solvation of cellulose in ILs; and (3) solution structure of cellulose solubilized in ILs. A coherent analysis of these modules will aid in better design of more efficient ILs and processes.

Related Literature

Infra-red spectroscopy of size selected Au25, Au38 and Au144ligand protected gold clusters

Mostafa Farrag, Martin Tschurl, Amala Dass, Ulrich Heiz

2013-06-05 Communication

DOI: 10.1039/C3CP51406D

Contributions of magnetic properties in epitaxial copper-doped ZnO

Hongyan Liu, Fei Zeng, Shuang Gao, Guangyue Wang, Cheng Song, Feng Pan

2013-07-03 Paper

DOI: 10.1039/C3CP51894A

Design and biophysical characterization of atrazine-sensing peptides mimicking the Chlamydomonas reinhardtiiplastoquinone binding niche

Viviana Scognamiglio, Pasquale Stano, Amina Antonacci, Maya Dimova Lambreva, Giorgio Pochetti, Maria Teresa Giardi, Giuseppina Rea

2013-06-03 Paper

DOI: 10.1039/C3CP51955D

Back cover

Cover

DOI: 10.1039/C3CP90070C

Cosolvent effects on the fibrillation reaction of human IAPP

Janine Seeliger, Kathrin Estel, Nelli Erwin, Roland Winter

2013-03-04 Paper

DOI: 10.1039/C3CP44412K

Tuning aromaticity patterns and electronic properties of armchair graphenenanoribbons with chemical edge functionalisation

Francisco J. Martin-Martinez, Stijn Fias, Gregory Van Lier, Frank De Proft, Paul Geerlings

2013-05-22 Paper

DOI: 10.1039/C3CP51293B

Improving the antifouling property of polysulfone ultrafiltration membrane by incorporation of isocyanate-treated graphene oxide

Haiyang Zhao, Liguang Wu, Zhijun Zhou, Lin Zhang, Huanlin Chen

2013-04-08 Paper

DOI: 10.1039/C3CP50955A

Large scale preparation of graphenequantum dots from graphite with tunable fluorescence properties

Yiqing Sun, Shiqi Wang, Chun Li, Peihui Luo, Lei Tao, Yen Wei, Gaoquan Shi

2013-04-24 Paper

DOI: 10.1039/C3CP50691F

Inside front cover

Cover

DOI: 10.1039/C3CP90064A

First-principles studies on transport properties and contact effects of Cu(111)/ZnO-nanobelt(100)/Cu(111) systems

Xu Sun, Yousong Gu, Xueqiang Wang, Yue Zhang

2013-05-31 Paper

DOI: 10.1039/C3CP50212K

You might also like

Compound Q&A

What are the main uses of 1H-Indazole-6-carbonitrile (CAS: 141290-59-7)?

1H-Indazole-6-carbonitrile finds applications in pharmaceuticals, where it serve...

141290-59-71H-Indazole-6-carbon...
Compound Q&A

How should waste containing Dioctyl (2E)-2-butenedioate (CAS: 2997-85-5) be handled?

Waste containing Dioctyl (2E)-2-butenedioate (CAS: 2997-85-5) should be collecte...

2997-85-5Dioctyl (2E)-2-buten...
Compound Q&A

What industries use Sodium [(1,2-benzoxazol-3-ylmethyl)sulfonyl]azanide (CAS: 68291-98-5)?

Sodium [(1,2-benzoxazol-3-ylmethyl)sulfonyl]azanide is primarily used in pharmac...

68291-98-5Sodium [(1,2-benzoxa...
Compound Q&A

Are there alternatives to Dimethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-pyridinedicarboxylate (CAS: 741709-66-0) in synthesis?

Dimethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,6-pyridinedicarboxyla...

741709-66-0Dimethyl 4-(4,4,5,5-...
Compound Q&A

How should waste containing 2-Fluoro-6-hydrazinopyridine (CAS: 80714-39-2) be handled?

Waste containing 2-Fluoro-6-hydrazinopyridine (CAS: 80714-39-2) should be manage...

80714-39-22-Fluoro-6-hydrazino...
Compound Q&A

What is 6-Formyl-2-pyridinecarboxylic acid (CAS: 499214-11-8)?

6-Formyl-2-pyridinecarboxylic acid is an organic compound with the molecular for...

499214-11-86-Formyl-2-pyridinec...
900874-91-13-(3,4-dimethoxyphen...
Compound Q&A

How is 9H-Tribenzo[b,d,f]azepine (CAS: 29875-73-8) typically synthesized?

9H-Tribenzo[b,d,f]azepine is typically synthesized via a multi-step process invo...

29875-73-89H-Tribenzo[b,d,f]az...
Compound Q&A

How is 1-Cyclopropyl-7-ethoxy-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid (CAS: 1797982-51-4) typically synthesized?

1-Cyclopropyl-7-ethoxy-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxyli...

1797982-51-41-Cyclopropyl-7-etho...
Compound Q&A

How should waste containing Methyl 3-oxo-1,2,3,4-tetrahydro-6-quinoxalinecarboxylate (CAS: 671820-52-3) be handled?

Waste containing Methyl 3-oxo-1,2,3,4-tetrahydro-6-quinoxalinecarboxylate (CAS: ...

671820-52-3Methyl 3-oxo-1,2,3,4...

Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.