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Pretreatment of Lignocellulosic Feedstocks
2017With the aim of reducing greenhouse gas (GHG) emissions and with our dependence on non-renewable fossil fuels, lignocellulose has been proposed to be an alternative sugar-rich raw material for renewable biofuel production, especially for the transportation sector.
Moreno, Antonio D., Olsson, Lisbeth
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Thermostable Enzymes in Lignocellulose Hydrolysis
2007Thermostable enzymes offer potential benefits in the hydrolysis of lignocellulosic substrates; higher specific activity decreasing the amount of enzymes, enhanced stability allowing improved hydrolysis performance and increased flexibility with respect to process configurations, all leading to improvement of the overall economy of the process.
Viikari, Liisa +5 more
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Lignocellulose: A chewy problem
Nature, 2011The inedible parts of plants are feeding the next generation of biofuels. But extracting the energy-containing molecules is a challenging task.
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Lignocellulose‐degrading marine fungi
Biofouling, 2000Evidence for lignocellulose-degrading ability among marine fungi is reviewed. Enzyme production, mass loss and micromorphological data suggest that most strains capable of decay activity are likely to be soft-rot fungi, with relatively few capable of white-rot decay.
Pointing, SB, Hyde, KD
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Applied Biochemistry and Biotechnology, 2007
Grass lignocelluloses are limited in bioconversion by aromatic constituents, which include both lignins and phenolic acids esters. Histochemistry, ultraviolet absorption microspectrophotometry, and response to microorganisms and specific enzymes have been used to determine the significance of aromatics toward recalcitrance.
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Grass lignocelluloses are limited in bioconversion by aromatic constituents, which include both lignins and phenolic acids esters. Histochemistry, ultraviolet absorption microspectrophotometry, and response to microorganisms and specific enzymes have been used to determine the significance of aromatics toward recalcitrance.
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Bioconversion of lignocellulosics
Biomass, 1990Abstract During the 3 years from 1986 to 1988, two International Energy Agency projects, CPD 2 (Pretreatment of Lignocellulosics) and CPD 5 (Conversion of C5, Sugars to Ethanol), were combined to form Task IV — Bioconversion of Lignocellulosics.
J.N. Saddler, K. Mackie
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Philosophical Transactions of the Royal Society of London. B, Biological Sciences, 1983
Abstract Sources of lignocellulose materials suitable for conversion into chemical feedstocks are reviewed and the chemical nature of the cellulosic, hemicellulosic and lignin components examined. Pulping and analytical methods of separation are discussed and a consideration is made of the potential products from lignocellulosic ...
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Abstract Sources of lignocellulose materials suitable for conversion into chemical feedstocks are reviewed and the chemical nature of the cellulosic, hemicellulosic and lignin components examined. Pulping and analytical methods of separation are discussed and a consideration is made of the potential products from lignocellulosic ...
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Polymers for Advanced Technologies, 2004
AbstractBanana pseudostem fiber which is a lignocellulosic material, relatively inexpensive, and abundantly available was assessed in terms of its fiber‐matrix adhesion and dispersion in composites. Different types of adhesives were used. The mechanical and water absorption properties were investigated.
Magda G. El‐Meligy +2 more
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AbstractBanana pseudostem fiber which is a lignocellulosic material, relatively inexpensive, and abundantly available was assessed in terms of its fiber‐matrix adhesion and dispersion in composites. Different types of adhesives were used. The mechanical and water absorption properties were investigated.
Magda G. El‐Meligy +2 more
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Mycoremediation of Lignocelluloses
2017The most abundant aromatic biopolymer on earth Lignin is extremely recalcitrant to degradation. It creates a barrier to solutions or enzymes by linking to both hemicellulose and cellulose preventing the penetration of lignocellulolytic enzymes into the interior lignocellulosic structure.
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