4.7 Article

Selective synthesis of 5-hydroxymethylfurfural over natural rubber-derived carbon/silica nanocomposites with acid-base bifunctionality

期刊

FUEL
卷 311, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2021.122577

关键词

Mesoporous carbon/silica composite; 5-Hydroxymethylfurfural; Hydrophobicity; Acid-base catalyst; Dehydration

资金

  1. Thailand Science Research and Innovation (TSRI) [PHD/0201/2560]
  2. International Research Network: Functional Porous Materials for Catalysis and Adsorption [IRN61W0003, RSA6280046]
  3. Center of Excellence in Catalysis for Bioenergy and Renewable Chemicals (CBRC)
  4. Center of Excellence on Petrochemical and Materials Technology (PETROMAT), Chulalongkorn University

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In this study, a mesoporous carbon/silica (MCS) nanocomposite was synthesized as a catalyst support for the production of 5-hydroxymethylfurfural (HMF) from glucose. By modifying the MCS surface, a series of acid-base catalysts were developed, and the acid-base properties could be tuned by adjusting the content of sulfonic acid and amino propyl groups. The developed MCS-SO3H-NH2 catalyst showed high HMF yield and selectivity when compared to other catalyst systems.
5-Hydroxymethylfurfural (HMF) is an important platform molecule, derived from biomass-based carbohydrates, for the production of renewable fuel additives, liquid hydrocarbon fuels, biopolymers, and specialty chemicals. In this study, a mesoporous carbon/silica (MCS) nanocomposite, as catalyst support, was prepared using a nano composite of natural rubber (NR) and hexagonal mesoporous silica (HMS) as a precursor. To obtain a series of acidic, basic, and bifunctional acid-base catalysts, the MCS surface was modified using post-synthesis methods in which the carbon moieties were decorated with sulfonic acid groups, whereas the silica matrix surface was grafted with 3-aminopropyl groups. The resulting materials exhibited high surface area, large pore volume, and contain some oxygen-containing functional groups. Their acid-base properties were tunable by varying the content of sulfonic acid and aminopropyl groups. The HMF was synthesized by catalytic conversion of fructose and glucose in a biphasic medium. Fructose dehydration catalyzed by sulfonated MCS catalyst (MCS-SO3H) at 150 degrees C for 2 h yields 56% HMF at 81% conversion. For the glucose system, the Bronsted basic sites facilitated the glucose-fructose isomerization, however, it promoted the formation of undesired humins. The acid/base ratio of bifunctional MCS catalysts (MCS-SO3H-NH2) contributes to the HMF yield and selectivity. The HMF yield of 39.4% was obtained over the MCS-SO3H-NH2 catalyst with an acid/base ratio of 0.10 at 190 degrees C for 1 h. In both systems, the formation of levulinic acid, a byproduct of HMF hydrolysis, was suppressed due to the hydrophobicity of the MCS catalyst. These developed catalysts are promising for the synthesis of HMF from glucose, at high substrate concentration than those reported in the literature.

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