Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/58434
Title: Preparation and investigation of highly selective solid acid catalysts with sodium lignosulfonate for hydrolysis of hemicellulose in corncob
Authors: Xun Li
Fengyao Shu
Chao He
Shuna Liu
Noppol Leksawasdi
Qiong Wang
Wei Qi
Md Asraful Alam
Zhenhong Yuan
Yi Gao
Authors: Xun Li
Fengyao Shu
Chao He
Shuna Liu
Noppol Leksawasdi
Qiong Wang
Wei Qi
Md Asraful Alam
Zhenhong Yuan
Yi Gao
Keywords: Chemical Engineering;Chemistry
Issue Date: 1-Jan-2018
Abstract: © The Royal Society of Chemistry 2018. Saccharification of lignocellulose is a necessary procedure for deconstructing the complex structure for building a sugar platform that can be used for producing biofuel and high-value chemicals. In this study, a carbon-based solid acid catalyst derived from sodium lignosulfonate, a waste by-product from the paper industry, was successfully prepared and used for the hydrolysis of hemicellulose in corncob. The optimum preparation conditions for the catalyst were determined to be carbonization at 250 °C for 6 h, followed by sulfonation with concentrated H2SO4(98%) and oxidation with 10% H2O2(solid-liquid ratio of 1:75 g mL-1) at 50 °C for 90 min. SEM, XRD, FT-IR, elemental analysis and acid-base titration were used for the characterization of the catalysts. It was found that 0.68 mmol g-1SO3H and 4.78 mmol g-1total acid were loaded onto the catalyst. When corncob was hydrolyzed by this catalyst at 130 °C for 12 h, the catalyst exhibited high selectivity and produced a relatively high xylose yield of up to 84.2% (w/w) with a few by-products. Under these conditions, the retention rate of cellulose was 82.5%, and the selectivity reached 86.75%. After 5 cycles of reuse, the catalyst still showed high catalytic activity, with slightly decreased yields of xylose from 84.2% to 70.7%.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85044200818&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/58434
ISSN: 20462069
Appears in Collections:CMUL: Journal Articles

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