2014
DOI: 10.1016/j.catcom.2014.07.035
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One-step preparation of carbonaceous solid acid catalysts by hydrothermal carbonization of glucose for cellulose hydrolysis

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Cited by 69 publications
(32 citation statements)
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“…A one-pot synthesis of -SO 3 H and COOH-functionalised carbon solid acids was successfully performed by hydrothermal carbonisation of glucose in the presence of sulfosalicylic acid and acrylic acid, respectively. 173 The functionalisation led to a change in the particles shape and resulted in good catalytic activity for the hydrolysis of cellulose. Importantly, the HSO 3functionalised carbon solid acid showed excellent stability up to five recycles without leaching of -SO 3 H species.…”
Section: Biomass-derived Carbon Catalystsmentioning
confidence: 99%
“…A one-pot synthesis of -SO 3 H and COOH-functionalised carbon solid acids was successfully performed by hydrothermal carbonisation of glucose in the presence of sulfosalicylic acid and acrylic acid, respectively. 173 The functionalisation led to a change in the particles shape and resulted in good catalytic activity for the hydrolysis of cellulose. Importantly, the HSO 3functionalised carbon solid acid showed excellent stability up to five recycles without leaching of -SO 3 H species.…”
Section: Biomass-derived Carbon Catalystsmentioning
confidence: 99%
“…According to the SEM micrographs, the hydrothermal carbon exhibited a uniform particle size whereas the CM‐SO 3 H particle showed a wide particle size distribution that resulted from the sulfonation step, which not only functionalized the carbon microspheres with sulfonic groups (SO 3 H) but also catalyzed the dehydration to furan compounds. The excess furan compounds promoted fast polymerization to grow nonuniform carbon particles . After KOH activation at 700°C and sulfonation, the morphology of the hydrothermal carbon (P‐C‐SO 3 H) contained cavities (diameter >50 nm), as shown in Figures c and d.…”
Section: Resultsmentioning
confidence: 98%
“…For example, the hydrothermal carbonization was performed for cellulose in the 220-250 °C range [40], for glucose between 170 and 500 °C [19,[41][42][43][44], for sucrose at 190 °C [45] and for starch at 600 °C [46]. Process times were typically between 4 and 12 h. For some of the materials, the graphitic nature has been improved by annealing the sample after synthesis.…”
Section: Discussionmentioning
confidence: 99%