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Issue 5, 2011
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Integrated production of nano-fibrillated cellulose and cellulosic biofuel (ethanol) by enzymatic fractionation of wood fibers

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Abstract

This study demonstrates the feasibility of integrating the production of nano-fibrillated cellulose (NFC), a potentially highly valuable biomaterial, with sugar/biofuel (ethanol) from wood fibers. Commercial cellulase enzymes were used to fractionate the less recalcitrant amorphous cellulose from a bleached Kraft eucalyptus pulp, resulting in a highly crystalline and recalcitrant cellulose (RC). The RC is difficult to hydrolyze to sugars but very suitable for producing biobased nanomaterials through mechanical homogenization. A range of fractionation yields of RC from 10–70% can be achieved by varying fractionation duration and enzyme dosage. The crystallinity of the RC was found to be as much as 24% higher than that of the original bleached pulp. The cellulase fractionation process facilitated mechanical homogenization by significantly reducing the degree of polymerization (DP) to about 400 and the length of the fibers to about 200 μm. The hydrolyzed sugars were found to be easily converted to ethanol through yeast fermentation with excellent efficiency of 92%. Films made from nano-fibrillated cellulose were found to be optically transparent, with opacity as low as 12%. The NFC films were mechanically strong and stiff, with tensile strengths and moduli approximately 10 and 6 times higher than film made from fibers that had not been nano-fibrillated.

Graphical abstract: Integrated production of nano-fibrillated cellulose and cellulosic biofuel (ethanol) by enzymatic fractionation of wood fibers

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Publication details

The article was received on 25 Jan 2011, accepted on 02 Mar 2011 and first published on 06 Apr 2011


Article type: Paper
DOI: 10.1039/C1GC15103G
Green Chem., 2011,13, 1339-1344

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    Integrated production of nano-fibrillated cellulose and cellulosic biofuel (ethanol) by enzymatic fractionation of wood fibers

    J. Y. Zhu, R. Sabo and X. Luo, Green Chem., 2011, 13, 1339
    DOI: 10.1039/C1GC15103G

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