2013
DOI: 10.1016/j.catcom.2013.06.005
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Preparation and performance evaluation of a lignin-based solid acid from acid hydrolysis lignin

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Cited by 35 publications
(24 citation statements)
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“…It is clear that lignin derived from CMF production (LCMF O ,e ntry 1) possesses ah igher surfacea rea in comparison to other types of lignin. [8] The trends observed between the increasing LCMF pyrolysis temperature ands urface area as well as pore volume are shown in Figure 8. [5] Yang et al have also reported BET surface areas for different types of lignin before furthert reatment:p urified Kraft lignin (6.9 m 2 g À1 ), ethanol-extracted lignin (12.6 m 2 g À1 )a nd diluted alkali lignin (0.6 m 2 g À1 ).…”
Section: Solid-state Nmr Spectroscopymentioning
confidence: 97%
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“…It is clear that lignin derived from CMF production (LCMF O ,e ntry 1) possesses ah igher surfacea rea in comparison to other types of lignin. [8] The trends observed between the increasing LCMF pyrolysis temperature ands urface area as well as pore volume are shown in Figure 8. [5] Yang et al have also reported BET surface areas for different types of lignin before furthert reatment:p urified Kraft lignin (6.9 m 2 g À1 ), ethanol-extracted lignin (12.6 m 2 g À1 )a nd diluted alkali lignin (0.6 m 2 g À1 ).…”
Section: Solid-state Nmr Spectroscopymentioning
confidence: 97%
“…For instance, Li and Luo optimised ap rocedure to create high-surface-area mesoporousc arbonsb yi mpregnation with sulfuric acid followed by pyrolysis at temperatures of 500 8C. [8] However, these materials only had low Similarly,H u and Hsieh demonstrated thatN aOH-activated carbon fibres can be madeb ye lectro-spinning alkali lignin followed by carbonisation at 850 8C.…”
Section: Introductionmentioning
confidence: 99%
“…This result provided that the presence of OH group in the catalyst. In addition, the FT-IR band at 1680 cm -1 shows that the carboxyl acid group presence at the structured sugar catalysts and this band is assigned to C=O stretching of COOH groups [13]. Moreover, peaks attribute to C-H and C-O-H asymmetric stretching for all sulfonated char catalysts are observed in the region of 1130-1150 cm -1 [14].…”
Section: Functional Groupsmentioning
confidence: 90%
“…The lignin-based solid acid also shows favorable catalytic activity on the esterification of acetic acid with ethanol and hydration of 2, 3-dimethyl-2butene. 175 Compared to conventional solid acid catalysts, e.g., strong acid cation exchange resin-Amberlyst 15 and sulfonated carbon, though the lignin-based solid acid has low concentration of SO 3 H groups, it has high catalytic activities over these two reactions. Such higher catalytic activity may be directly related to the contribution of the abundant macroporosity, which has an advantage for mass transfer, achieving good accessibility for reactants in solution to SO 3 H groups.…”
Section: Catalysis Applicationsmentioning
confidence: 99%