2022
DOI: 10.1016/j.crgsc.2022.100305
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Conversion of xylose to bioproducts on bifunctional supported platinum-group metals catalysts

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Cited by 3 publications
(4 citation statements)
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“…It suggests that competitive side reactions predominantly take place from furfuryl alcohol at high acid concentrations, deterring its hydrolysis to valuable bioproducts. Acid‐catalyzed conversion of furfuryl alcohol to higher molecular weight compounds and polymeric species has indeed been usually reported in the literature [13,14,15,55] . 2,2’‐difurfuryl ether and 2,2’‐difurfurylmethane were identified by GC‐MS in this study, showing that etherification and homopolycondensation of furfuryl alcohol are also promoted along with its eventual degradation/polymerization (Figure 5).…”
Section: Resultssupporting
confidence: 83%
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“…It suggests that competitive side reactions predominantly take place from furfuryl alcohol at high acid concentrations, deterring its hydrolysis to valuable bioproducts. Acid‐catalyzed conversion of furfuryl alcohol to higher molecular weight compounds and polymeric species has indeed been usually reported in the literature [13,14,15,55] . 2,2’‐difurfuryl ether and 2,2’‐difurfurylmethane were identified by GC‐MS in this study, showing that etherification and homopolycondensation of furfuryl alcohol are also promoted along with its eventual degradation/polymerization (Figure 5).…”
Section: Resultssupporting
confidence: 83%
“…Acid-catalyzed conversion of furfuryl alcohol to higher molecular weight compounds and polymeric species has indeed been usually reported in the literature. [13,14,15,55] 2,2'-difurfuryl ether and 2,2'difurfurylmethane were identified by GC-MS in this study, showing that etherification and homopolycondensation of furfuryl alcohol are also promoted along with its eventual ChemCatChem degradation/polymerization (Figure 5). Contribution from the formation of higher molecular weight compounds from the desired bioproducts cannot be overlooked though.…”
Section: Chemcatchemmentioning
confidence: 56%
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“…Xylose accounts for approximately 20-30% by weigh of lignocellulosic biomass, and d-xylose (wood sugar) is the main structure of hemicellulose [20]. The monosaccharides in cellulose and hemicellulose are released through hydrolysis [21]. Therefore, the detected acids could be generated via the hydrolysis of hemicellulose, and the dehydration reactions of d-xylose [22,23] or lignin side chains [6,24].…”
Section: Organic Acid and Total Organic Carbon Analysesmentioning
confidence: 99%