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Biohydrogen production from photodecomposition of various cellulosic biomass wastes using metal-TiO2 catalysts

Biohydrogen generation from direct photocatalytic decomposition of lignocellulose biomass waste was investigated using TiO 2 with metal co-catalysts. The behavior of the photocatalyst was explored by studying the effect of metal co-catalysts (Pd, Cu, Ni, Ce) and the amount of metal loading. The reac...

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Bibliographic Details
Published in:Biomass conversion and biorefinery 2023-07, Vol.13 (10), p.8701-8712
Main Authors: Abdul Razak, Syaahidah, Mahadi, Abdul Hanif, Abdullah, Rosnah, Yasin, Hartini Mohd, Ja’afar, Fairuzeta, Abdul Rahman, Norizah, Bahruji, Hasliza
Format: Article
Language:English
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Summary:Biohydrogen generation from direct photocatalytic decomposition of lignocellulose biomass waste was investigated using TiO 2 with metal co-catalysts. The behavior of the photocatalyst was explored by studying the effect of metal co-catalysts (Pd, Cu, Ni, Ce) and the amount of metal loading. The reactivity of TiO 2 was found to vary depending on the metal co-catalysts, with the order of reactivity being Pd > Cu > Ni = Ce. Cellulose samples extracted from coconut husk, fern fiber, and cotton linter were characterized using XRD, FTIR, and SEM analysis. Crystallinity index (CI), degree of polymerization (DP), and α-cellulose and hemicellulose concentrations were correlated with hydrogen yield. Cotton linter cellulose with high CI and DP produced 131 μmol of H 2 in 3 h followed by cellulose extracted from coconut husk at 38 μmol and fern fibers at 6 μmol. High concentrations of hemicellulose enhanced the rate of H 2 production due to the release of acetic acid during photodecomposition and accelerated the hydrolysis. Sugar fractions containing glucose and fructose obtained from hydrothermal treatment of cotton linter cellulose improved H 2 yield, which suggests that the rate limiting step of the reaction is the dissociation of β(1→4)-glycosidic bonds to form sugar monomers.
ISSN:2190-6815
2190-6823
DOI:10.1007/s13399-020-01164-4