Abstract
Lignocellulosic materials such as wood, grass, and agricultural and forest residues are promising alternative energy resources that can be utilized to produce ethanol. The yield of ethanol production from native lignocellulosic material is relatively low due to its native recalcitrance, which is attributed to, in part, lignin content/structure, hemicelluloses, cellulose crystallinity, and other factors. Pretreatment of lignocellulosic materials is required to overcome this recalcitrance. The goal of pretreatment is to alter the physical features and chemical composition/structure of lignocellulosic materials, thus making cellulose more accessible to enzymatic hydrolysis for sugar conversion. Various pretreatment technologies to reduce recalcitrance and to increase sugar yield have been developed during the past two decades. This review examines the changes in lignocellulosic structure primarily in cellulose and hemicellulose during the most commonly applied pretreatment technologies including dilute acid pretreatment, hydrothermal pretreatment, and alkaline pretreatment.
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Abbreviations
- DAP:
-
Dilute acid pretreatment
- DP:
-
Degree of polymerization
- LCC:
-
Lignin–carbohydrate complex
- CS:
-
Combined severity
- LODP:
-
Leveling-off degree of polymerization
- CP:
-
Cross-polarization
- MAS:
-
Magnetic angle spin
- NMR:
-
Nuclear magnetic resonance
- HMF:
-
5-Hydroxymethylfurfural
- SEM:
-
Scanning electron microscope
- LHW:
-
Liquid hot water
- AFEX:
-
Ammonia fiber explosion
- ARP:
-
Ammonia recycled percolation
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The authors are grateful for the financial support from the Paper Science & Engineering (PSE) fellowship program at Institute of Paper Science & Technology (IPST) and the School of Chemistry and Biochemistry at Georgia Institute of Technology.
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Hu, F., Ragauskas, A. Pretreatment and Lignocellulosic Chemistry. Bioenerg. Res. 5, 1043–1066 (2012). https://doi.org/10.1007/s12155-012-9208-0
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DOI: https://doi.org/10.1007/s12155-012-9208-0