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Original Article | Open Access

Toward Sustainable, Economic, and Tailored Production of Cellulose Nanomaterials

HuiYang Bian1JunYong Zhu2( )LiHeng Chen3Roland Gleisner2
Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Nanjing Forestry University, Nanjing, Jiangsu Province, 210037, China
USDA Forest Products Laboratory, Madison, Wisconsin, 53726, USA
Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Department of Biomedical Engineering, Ji'nan University, Guangzhou, Guangdong Province, 510632, China
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Abstract

This paper introduces a concentrated di-carboxylic acid (DCA) hydrolysis process for the integrated production of thermally stable and carboxylated cellulose nanocrystals (CNCs) and cellulose nanofibrils (CNFs). The DCA hydrolysis process addressed several issues associated with mineral acid hydrolysis for CNC production, such as cellulose loss and acid recovery. The surface and morphological properties of the cellulose nanomaterials resulting from the DCA hydrolysis process can be tailored simply by controlling the severity of DCA hydrolysis. To further reduce cost, a lowtemperature (≤80 ℃) hydrotropic chemical process using p-toluenesulfonic acid (p-TsOH) was also introduced to rapidly fractionate raw lignocelluloses for the production of lignin containing cellulose nanofibrils (LCNFs) and lignin nanoparticles (LNPs). The LCNF surface hydrophobicity and morphology can be tailored by controlling the fractionation severity, i.e., the extent of delignification. The lignin also improved the thermal stability of LCNFs. LNPs can be easily separated by diluting the spent acid liquor to below the p-TsOH minimal hydrotropic concentration of approximately 10%. p-TsOH can also be easily recovered by re-concentrating the diluted spent liquor after lignin precipitation. We believe that these two novel processes presented here have the potential to achieve true sustainable, economic, and tailored production of cellulose nanomaterials, suitable for a variety of applications.

References

[1]

Zhu H, Luo W, Ciesielski P N, et al. Wood-derived materials for green electronics, biological devices, and energy applications[J]. Chem Rev, 2016, 116 (16): 9305-9374.

[2]

Moon R J, Martini A, Nairn J, et al. Cellulose nanomaterials review: structure, properties and nanocomposites[J]. Chem Soc Rev, 2011, 40: 3941-3994.

[3]

Kelly J A, Shukaliak A M, Cheung C C Y, et al. Responsive photonic hydrogels based on nanocrystalline cellulose[J]. Angew Chem Int Ed, 2013, 52 (34): 8912-8916.

[4]

Chen L, Wang Q, Hirth K, et al. Tailoring the yield and characteristics of wood cellulose nanocrystals (CNC) using concentrated acid hydrolysis[J]. Cellulose, 2015, 22: 1753-1762.

[5]

Reid M S, Villalobos M, Cranston E D. Benchmarking cellulose nanocrystals: From the laboratory to industrial production[J]. Langmuir, 2017, 33 (7): 1583-1598.

[6]

Dong X M, Revol J F, Gray D G. Effect of microcrystallite preparation conditions on the formation of colloid crystals of cellulose[J]. Cellulose, 1998, 5: 19-32.

[7]

Wang Q, Zhao X, Zhu J Y. Kinetics of strong acid hydrolysis of a bleached kraft pulp for producing cellulose nanocrystals (CNCs)[J]. Ind Eng Chem Res, 2014, 53 (27): 11007-11014.

[8]

Wang Q Q, Zhu J Y, Reiner R S, et al. Approaching zero cellulose loss in cellulose nanocrystal (CNC) production: recovery and characterization of cellulosic solid residues (CSR) and CNC[J]. Cellulose, 2012, 19 (6): 2033-2047.

[9]

Wang Q Q, Zhu J Y, Gleisner R, et al. Morphological development of cellulose fibrils of a bleached eucalyptus pulp by mechanical fibrillation[J]. Cellulose, 2012, 19 (5): 1631-1643.

[10]

Rojo E, Peresin M S, Sampson W W, et al. Comprehensive elucidation of the effect of residual lignin on the physical, barrier, mechanical, and surface properties of nanocellulose films[J]. Green Chem, 2015, 17: 1853-1866.

[11]

Iwamoto S, Nakagaito A N, Yano H. Nano-fibrillation of pulpfibers for the processing of transparent nanocomposites[J]. Applied Physics A: Materials Science and Processing, 2007, 89: 461-466.

[12]

Sehaqui H, Kulasinski K, Pfenninger N, et al. Highly carboxylated cellulose nanofibers via succinic anhydride esterification of wheat fibers and facile mechanical disintegration[J]. Biomacmolecules, 2017, 18 (1): 242-248.

[13]

Qin Y, Qiu X, Zhu J Y. Understanding longitudinal wood fiber ultra-structure for producing cellulose nanofibrils using disk milling with dilute acid prehydrolysis[J]. Sci Rep, 2016, 6: 35602.

[14]

Saito T, Nishiyama Y, Putaux J L, et al. Homogeneous suspensions of individua lizedmicr of ibrils from TEMPO-catalyzed oxidation of native cellulose[J]. Biomacromolecules, 2006, 7 (6): 1687-1691.

[15]

Liimatainen H, Visanko M, SirviöJ A, et al. Enhancement of the nanofibrillation of wood cellulose through sequential periodate-chlorite oxidation[J]. Biomacromolecules, 2012, 13 (5): 1592-1597.

[16]

Wang W, Mozuch M D, Sabo R C, et al. Production of cellulose nanofibrils from bleached eucalyptus fibers by hyperthermostable endoglucanase treatment and subsequent microfluidization[J]. Cellulose, 2015, 22: 351-361.

[17]

Pääkko M, Ankerfors M, Kosonen H, et al. Enzymatic hydrolysis combined with mechanical shearing and highpressure homogenization for nanoscale cellulose fibrils and strong gels[J]. Biomacromolecules, 2007, 8: 1934-1941.

[18]

Chen L, Zhu J Y, Baez C, et al. Highly thermal-stable and functional cellulose nanocrystals and nanofibrils produced using fully recyclable organic acids[J]. Green Chem, 2016, 18: 3835-3843.

[19]

Bian H, Chen L, Wang R, et al. Green and low-cost production of thermally stable and carboxylated cellulose nanocrystals and nanofibrils using highly recyclable dicarboxylic acids[J]. J Visualized Exp, 2017, DOI:10.3791/55079.

[20]

Wang R, Chen L, Zhu J Y, et al. Tailored and integrated production of carboxylated cellulose nanocrystals (CNC) with nanofibrils (CNF) through maleic acid hydrolysis[J]. Chem Nano Mat, 2017, 3 (5): 328-335.

[21]

Bian H, Chen L, Dai H, et al. Integrated production of lignin containing cellulose nanocrystals (LCNC) and nanofibrils (LCNF) using an easily recyclable dicarboxylic acid[J]. Carbohydrate Polymers, 2017, 167: 167-176.

[22]

Bian, H, Chen L, Gleisner R, et al. Producing wood-based nanomaterials by rapid fractionation of wood at 80 ℃ using a recyclable acid hydrotrope[J]. Green Chem, 2017, 19: 3370-3379.

Paper and Biomaterials
Pages 1-7
Cite this article:
Bian H, Zhu J, Chen L, et al. Toward Sustainable, Economic, and Tailored Production of Cellulose Nanomaterials. Paper and Biomaterials, 2017, 2(4): 1-7. https://doi.org/10.26599/PBM.2017.9260022

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Received: 12 July 2017
Accepted: 20 August 2017
Published: 25 October 2017
© 2017 Paper and Biomaterials Editorial Board

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)

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