Campus Units

Chemical and Biological Engineering, NSF Engineering Research Center for Biorenewable Chemicals

Document Type

Article

Research Focus Area

Catalysis and Reaction Engineering, Renewable Energy

Publication Version

Submitted Manuscript

Publication Date

10-18-2018

Journal or Book Title

ACS Sustainable Chemistry & Engineering

DOI

10.1021/acssuschemeng.8b02752

Abstract

In this work, glucose isomerization to fructose was conducted via a solid base biochar catalyst derived from spent coffee grounds and melamine. The X-ray photoelectron spectroscopy (XPS) spectra identified the majority of pyridinic nitrogen on the biochar surface, which imparted the strong base character of the catalyst. Activity of the catalyst was evidenced by fast conversion of glucose (12%) and high selectivity to fructose (84%) in 20 min at a moderate temperature (120 °C) compared to recently reported immobilized tertiary amines at comparable N concentrations (10-15 mol% relative to glucose). By increasing the reaction temperature to 160 °C, fructose yield achieved 14% in 5 min. The base biochar catalyst showed superior selectivity (>80%) to commonly used homogeneous base catalysts such as aqueous hydroxides and amines (50-80%) and comparable catalytic activity (~20 mol% conversion within 20 min). Moreover, co-solvent of acetone in the reaction system may increase the overall basicity by stabilizing protonated water clusters via hydrogen bonding, which led to faster conversion and higher fructose selectivity than those in water. Approximately 19% fructose was obtained at 160 °C, and the basic sites on the biochar catalyst were stable in hydrothermal environment as indicated by acid-base titration test. Therefore, nitrogen-doped engineered biochar can potentially serve as solid base catalyst for biorefinery processes.

Comments

This document is the unedited Author’s version of a Submitted Work that was subsequently accepted for publication in ACS Sustainable Chemistry & Engineering, copyright © American Chemical Society after peer review. To access the final edited and published work see DOI: 10.1021/acssuschemeng.8b02752. Posted with permission.

Copyright Owner

American Chemical Society

Language

en

File Format

application/pdf

Published Version

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