Preparation of a novel carbon-based solid acid from cocarbonized starch and polyvinyl chloride for cellulose hydrolysis

•CCSA was prepared from cocarbonized starch and PVC followed by sulfonation.•The ether (C–O–C) and aliphatic (–CH2–) bridges make carbon sheets fully stretch.•Covalent chlorine tends to form hydrogen bonds with cellulose hydroxyl groups.•Based on the above two points, reducing sugar yield improves b...

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Veröffentlicht in:Applied catalysis. A, General General, 2014-03, Vol.473, p.70-74
Hauptverfasser: Shen, Shuguang, Cai, Bei, Wang, Chunyan, Li, Huanmei, Dai, Guang, Qin, Haifeng
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container_end_page 74
container_issue
container_start_page 70
container_title Applied catalysis. A, General
container_volume 473
creator Shen, Shuguang
Cai, Bei
Wang, Chunyan
Li, Huanmei
Dai, Guang
Qin, Haifeng
description •CCSA was prepared from cocarbonized starch and PVC followed by sulfonation.•The ether (C–O–C) and aliphatic (–CH2–) bridges make carbon sheets fully stretch.•Covalent chlorine tends to form hydrogen bonds with cellulose hydroxyl groups.•Based on the above two points, reducing sugar yield improves by approximately 57%.•The good stability may be attributed to resonance effect among Cl and aromatic rings. A novel carbon-based solid acid was successfully prepared by sulfonation of cocarbonized starch and polyvinyl chloride (PVC). The characterization results show that this catalyst possesses all characteristics of traditional carbon-based solid acids (CSAs). The differences are that chlorine from PVC is covalently bonded to edges of aromatic carbon sheets as new active groups, and ether (C–O–C) and aliphatic (–CH2–) bridges are formed during the cocarbonization process which are derived from oxygen in starch and alkyl in PVC, respectively. Chlorine groups can adsorb cellulose hydroxyl groups strongly and bridge bonds make the carbon framework fully stretch, which reduces hindrance between SO3H groups and glycosidic bonds to promote the catalytic performance in cellulose hydrolysis experiments. Furthermore, the durability results indicate that this catalyst has good stability.
doi_str_mv 10.1016/j.apcata.2013.12.037
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A novel carbon-based solid acid was successfully prepared by sulfonation of cocarbonized starch and polyvinyl chloride (PVC). The characterization results show that this catalyst possesses all characteristics of traditional carbon-based solid acids (CSAs). The differences are that chlorine from PVC is covalently bonded to edges of aromatic carbon sheets as new active groups, and ether (C–O–C) and aliphatic (–CH2–) bridges are formed during the cocarbonization process which are derived from oxygen in starch and alkyl in PVC, respectively. Chlorine groups can adsorb cellulose hydroxyl groups strongly and bridge bonds make the carbon framework fully stretch, which reduces hindrance between SO3H groups and glycosidic bonds to promote the catalytic performance in cellulose hydrolysis experiments. 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A, General</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Shuguang</au><au>Cai, Bei</au><au>Wang, Chunyan</au><au>Li, Huanmei</au><au>Dai, Guang</au><au>Qin, Haifeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of a novel carbon-based solid acid from cocarbonized starch and polyvinyl chloride for cellulose hydrolysis</atitle><jtitle>Applied catalysis. 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subjects Bridges (structures)
Carbon
Carbon-based solid acid
Catalysts
Cellulose
Chlorine
Cocarbonization
Heterogeneous hydrolysis
Hydrolysis
Polyvinyl chlorides
Starches
title Preparation of a novel carbon-based solid acid from cocarbonized starch and polyvinyl chloride for cellulose hydrolysis
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