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Original Article | Open Access

Comparative Study of Isolated Polysaccharides from Triploid Poplar Using Different Solvents and Chemicals

YingYing Chai1Ning Zhao1YunShan Ju1QingTao Fan2Kun Wang1( )
Beijing Key Laboratory of Lignocellulosic Chemistry, MOE Engineering Research Center of Forestry Biomass Materials and Bioenergy, College of Materials Science and Technology, Beijing Forestry University, Beijing 100083, China
Beijing Institute of Science and Technology Information, Beijing 100044, China
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Abstract

The conversion of lignocellulose to value-added products is normally focused on fuel production; however, large-scale biorefineries require a cost-effective pretreatment process that can effectively fractionate the three main constituents of lignocellulose for the production of chemicals, fuels, and materials. In this study, a hemicellulosic biopolymer from poplar was fractionated by a mild organosolv process and the effects of various chemicals (sodium hydroxide, triethylamine, and formic acid) and alcohols on the fractionation efficiency and structural variation of hemicellulose were examined. Comparative studies indicated that an acidic catalyst decreased the purity of hemicelluloses by partial degradation of cellulose, and the core of the hemicellulosic biomacromolecule could be released and dissolved under alkaline conditions with 5.8%~19.0% yields. In addition, the use of alcohol with longer alkyl chains facilitated the release of the hemicellulosic biomacromolecule by partially cleaving the ether bonds in the lignin-carbohydrate complex (LCC); this is probably due to steric hindrance. The thermal degradation behavior showed that complete pyrolysis was easily achieved for the hemicellulosic polymer with minimal branches irrespective of its molecular weight.

References

[1]

Sultana A, Kumar A. Optimal configuration and combination of multiple lignocellulosic biomass feedstocks delivery to a biorefinery[J]. Bioresource Technology, 2011, 102(21): 9947-9956.

[2]

Smit A, Huijgen W. Effective fractionation of lignocellulose in herbaceous biomass and hardwood using a mild acetone organosolv process[J]. Green Chemistry, 2017, 19(22): 5505-5514.

[3]

Lynd L R, Laser M S, Bransby D, et al. How biotech can transform biofuels[J]. Nature Biotechnology, 2008, 26(2): 169-172.

[4]

Longati A, Lino A R A, Giordano R C, et al. Defining research & development process targets through retro-technoeconomic analysis: the sugarcane biorefinery case[J]. Bioresource Technology, 2018, 263: 1-9.

[5]

Hassan S S, Williams G A, Jaiswal A K. Emerging technologies for the pretreatment of lignocellulosic biomass[J]. Bioresource Technology, 2018, 262: 310-318.

[6]

Willfor S, Sundberg A, Pranovich A, et al. Polysacharides in some industrially important hardwood species[J]. Wood Science and Technology, 2005, 39(8): 601-617.

[7]

Gnansounou E, Dauriat A. Techno-economic analysis of lignocellulosic ethanol: a review[J]. Bioresource Technology, 2010, 101(13): 4980-4991.

[8]

Cao Z, Dierks M, Clough M T, et al. A convergent approach for a deep converting lignin-first biorefinery rendering high-energy-density drop-in fuels[J]. Joule, 2018, 2: 1118-1133.

[9]

Thomsen M H, Thygesen A, Thomsen A B. Hydrothermal treatment of wheat straw at pilot plant scale using a threestep reactor system aiming at high hemicellulose recovery, high cellulose digestibility and low lignin hydrolysis[J]. Bioresource Technology, 2008, 99(10): 4221-4228.

[10]

Santos T M, Alonso M V, Oliet M, et al. Effect of autohydrolysis on Pinus radiata wood for hemicellulose extraction[J]. Carbohydrate Polymers, 2018, 194: 285-293.

[11]

Alvarez-Vasco C, Guo M, Zhang X. Dilute acid pretreatment of Douglas fir forest residues: pretreatment yield, hemicellulose degradation, and enzymatic hydrolysability[J]. Bioenergy Research, 2015, 8(1): 42-52.

[12]

Goldmann W M, Ahola J, Mikola M, et al. Formic acid aided hot water extraction of hemicellulose from European silver birch (Betula pendula) sawdust[J]. Bioresource Technology, 2017, 232: 176-182.

[13]

Wei L, Yan T, Wu Y, et al. Optimization of alkaline extraction of hemicellulose from sweet sorghum bagasse and its direct application for the production of acidic xylooligosaccharides by Bacillus subtilis strain MR44[J]. PLoS ONE, 2018, DOI: 10.1371/journcl.pone.0195616.

[14]

Shahabazuddin M, Chandra T S, Meena S, et al. Thermal assisted alkaline pretreatment of rice husk for enhanced biomass deconstruction and enzymatic saccharification: physico-chemical and structural characterization[J]. Bioresource Technology, 2018, 263: 199-202.

[15]

Martin-Sampedro R, Eugenio M E, Moreno J A, et al. Integration of a kraft pulping mill into a forest biorefinery: Pre-extraction of hemicellulose by steam explosion versus steam treatment[J]. Bioresource Technology, 2014, 153: 236-244.

[16]

Minjares-Fuentes R, Femenia A, Garau M C, et al. Ultrasound-assisted extraction of hemicelluloses from grape pomace using response surface methodology[J]. Carbohydrate Polymers, 2016, 138: 180-191.

[17]

Egues I, Sanchez C, Mondragon I, et al. Separation and purification of hemicellulose by ultrafiltration[J]. Industrial & Engineering Chemistry Research, 2012, 51(1): 523-530.

[18]

Singh S C, Murthy Z V P. Hemicelluloses separation from caustic-containing process stream by ultrafiltration[J]. Separation Science and Technology, 2017, 14: 2252-2261.

[19]

Cateto C, Hu G, Ragauskas A. Enzymatic hydrolysis of organosolv Kanlow switchgrass and its impact on cellulose crystallinity and degree of polymerization[J]. Energy & Environmental Science, 2011, 4(4): 1516-1521.

[20]

Huijgen W J, Smit A T, Reith J H, et al. Catalytic organosolv fractionation of willow wood and wheat straw as pretreatment for enzymatic cellulose hydrolysis[J]. Journal of Chemical Technology and Biotechnology, 2011, 86(11): 1428-1438.

[21]

Mesa L, Lopez N, Cara C, et al. Techno-economic evaluation of strategies based on two steps organosolv pretreatment and enzymatic hydrolysis of sugarcane bagasse for ethanol production[J]. Renewable Energy, 2016, 86: 270-279.

[22]

Zhu Z T, Zhang Z Y. The status and advances of genetic improvement of Populus tomentosa Carr.[J]. Journal of Beijing Forestry University, 1997, 6: 1-7.

[23]

Wang K, Yang H Y, Xu F, et al. Structural comparison and enhanced enzymatic hydrolysis of the cellulosic preparation from Populus tomentosa Carr., by different cellulose-soluble solvent systems[J]. Bioresource Technology, 2011, 102(6): 4524-4529.

[24]

Wang K, Yang H Y, Yao X, et al. Structural transformation of hemicelluloses and lignin from triploid poplar during acid-pretreatment based biorefinery process[J]. Bioresource Technology, 2012, 116: 99-106.

[25]

Gilarranz M A, Rodriguez F, Oliet M. Lignin behavior during the autocatalyzed methanol pulping of eucalyptus globulus changes in molecular weight and functionality[J]. Holzforschung, 2000, 54(4): 373-380.

[26]

Wang K, Yang H Y, Guo S H, et al. Comparative characterization of degraded lignin polymer from the organosolv fractionation process with various catalysts and alcohols[J]. Journal of Applied Polymer and Science, 2013, 131(1): 1-15.

[27]

Wang K, Jiang J X, Xu F, et al. Influence of steaming explosion time on the physic-chemical properties of cellulose from Lespedeza stalks (Lespedeza crytobotrya)[J]. Bioresource Technology, 2009, 100(21): 5288-5294.

[28]
Sluiter A, Hames B, Ruiz R, et al. Determination of structural carbohydrates and lignin in biomass[S/OL]. National Renewable Energy Laboratory (NREL) Laboratory Analytical Procedures (LAP) for Standard Biomass Analysis. https://wenku.baidu.com/view/5f23c8c904a1b0717ed5dd02.html.
[29]

Wang K, Jiang J X, Xu F, et al. Effects of incubation time on the fractionation and characterization of lignin during steam explosion pretreatment[J]. Industrial & Engineering Chemistry Research, 2012, 51: 2704-2713.

[30]

Wang K, Xu F, Sun R C, et al. Influence of incubation time on the physicochemical properties of the isolated hemicelluloses from steam-exploded lespedeza stalks[J]. Industrial & Engineering Chemistry Research, 2010, 49(18): 8797-8804.

[31]

Chen L M, Wilson R H, McCann M C. Investigation of macromolecule orientation in dry and hydrated walls of single onion epidermal cells by FT-IR microspectroscopy[J]. Journal of Molecular Structure, 1997, 408-409: 257-260.

[32]

Sun R C, Fang J M, Rowlands P, et al. Physicochemical and thermal characterization of wheat straw hemicelluloses and cellulose[J]. Journal of Agricultural and Food Chemistry, 1998, 46(7): 2804-2809.

[33]

Yang H P, Yan R, Chen H P, et al. Characteristics of hemicellulose, cellulose and lignin pyrolysis[J]. Fuel, 2007, 86(12): 1781-1788.

[34]

Demirbas A, Gullu D. Acetic acid, methanol and acetone from lignocellulosics by pyrolysis[J]. Energy Education Science and Technology, 1998, 2: 111-115.

Paper and Biomaterials
Pages 7-16
Cite this article:
Chai Y, Zhao N, Ju Y, et al. Comparative Study of Isolated Polysaccharides from Triploid Poplar Using Different Solvents and Chemicals. Paper and Biomaterials, 2019, 4(1): 7-16. https://doi.org/10.26599/PBM.2019.9260002

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Received: 28 August 2018
Accepted: 10 October 2018
Published: 01 January 2019
© 2019 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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