Journal
RSC ADVANCES
Volume 4, Issue 88, Pages 47448-47454Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra07747d
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Funding
- National Science Foundation [CAREER DMR-0747667]
- Nevada Renewable Energy Consortium
- KUSCO WEST Program
- Division Of Materials Research
- Direct For Mathematical & Physical Scien [1261331] Funding Source: National Science Foundation
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A polystyrene-supported superacidic fluoroalkyl sulfonic acid catalyst (sPS-S) was synthesized using a combination of iridium-catalyzed C-H borylation and Suzuki-Miyaura coupling reactions. Catalytic activity of the new solid acid catalyst was examined for esterification of fatty acids and transesterification of triglyceride with methanol. Significantly higher activity than those of commercial sulfonated ion-exchange resins (Amberlyst 15 and Nafion NR50) was achieved with a catalyst loading as low as 0.5 wt%. The solid catalyst could be easily recovered by filtration and reused. Consistently high activities were obtained from the esterification for up to ten consecutive runs.
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