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Transforming Lignocelluloses to Suga...
~
Shuai, Li.
Transforming Lignocelluloses to Sugars and Liquid Fuels.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Transforming Lignocelluloses to Sugars and Liquid Fuels.
作者:
Shuai, Li.
面頁冊數:
223 p.
附註:
Source: Dissertation Abstracts International, Volume: 73-12(E), Section: B.
附註:
Adviser: Xuejun Pan.
Contained By:
Dissertation Abstracts International73-12B(E).
標題:
Engineering, Agricultural.
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3519236
ISBN:
9781267519351
Transforming Lignocelluloses to Sugars and Liquid Fuels.
Shuai, Li.
Transforming Lignocelluloses to Sugars and Liquid Fuels.
- 223 p.
Source: Dissertation Abstracts International, Volume: 73-12(E), Section: B.
Thesis (Ph.D.)--The University of Wisconsin - Madison, 2012.
Extensive research has been done for cost-effectively producing sugars and sugar derivatives from lignocelluloses. In this thesis, a few new processes of converting lignocelluloses into sugars and liquid fuels are presented.
ISBN: 9781267519351Subjects--Topical Terms:
264349
Engineering, Agricultural.
Transforming Lignocelluloses to Sugars and Liquid Fuels.
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Extensive research has been done for cost-effectively producing sugars and sugar derivatives from lignocelluloses. In this thesis, a few new processes of converting lignocelluloses into sugars and liquid fuels are presented.
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First, a sulfite pretreatment (SPORL--Sulfite Pretreatment to Overcome Recalcitrance of Lignocelluloses) was demonstrated to be more effective to enhance enzymatic digestibility of woody biomass like spruce than dilute acid pretreatment. Addition of sulfite along with sulfuric acid partially dissolved lignin and sulfonated residual lignin in the SPORL substrate, which reduced non-productive adsorption of enzymes on lignin. The buffer effect of sulfite protected cellulose and hemicellulose from extensive acidic hydrolysis and further decomposition. Therefore, SPORL recovered more fermentable sugars and generated less fermentation inhibitors than DA pretreatment.
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Second, a polystyrene-based cellulase-mimetic solid acid with both cellulose binding domain (-Cl) and catalytic domain (-SO3H) was synthesized for cellulose hydrolysis. The binding domain facilitated the association of substrate onto the catalyst surface and therefore accelerated the cellulose hydrolysis. The cellulose hydrolysis catalyzed by the solid acid had much lower apparent activation energy than the ones catalyzed by liquid acids and general solid acids without binding domains.
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Third, a one-step process was developed for direct saccharification of lignocelluloses at moderate temperature in concentrated metal halide solution without pretreatment. Fed-batch of biomass allowed to produce a concentrated sugar solution for downstream processing. Sugars and the salt were separated through a combination of solvent extraction of salt and ion-exchange chromatography or other techniques.
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Fourth, a one-pot process was developed for transforming lignocellulose into furan-based precursors for hydrocarbon fuels without pretreatment or saccharification. In a LiBr/acetone system with small amount of acid, unsolvated Li+ and Br- rapidly disrupted hydrogen bonds in cellulose crystals and facilitated the hydrolysis of cellulose and hemicellulose. Br- further catalyzed the dehydration of sugars into hydroxymethylfurfural (or furfural), which subsequently reacted with acetone through aldol-condensation to form furan-based precursors with 5-21 carbons in high yield and selectivity. Lignin was extensively depolymerized into low-molecular-weight fragments that can be hydrodeoxygenated together with the precursors into hydrocarbon fuels. The lignin also had good potential for high-value co-products development.
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http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3519236
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