Abstract

Lignin depolymerization often requires multiple isolation steps to convert a lignocellulose matrix into high-value chemicals. In addition, lignin structural modification, low yields, and poor product characteristics remain challenges. Direct catalytic depolymerization of lignocellulose from date palm biomass was investigated. Production of high value chemicals heavily depends on optimization of different parameters and method of conversion. The goal of the study was to elucidate the role of different parameters on direct conversion of date palm waste in a bench reactor, targeting valuable C5–C12 compounds. The catalytic performance results demonstrated better liquid yields using a commercial alloy catalyst than with laboratory-prepared transition metal phosphide catalysts made using nickel, cobalt, and iron. According to the gas chromatography-mass spectrometry results, C7–C8 compounds were the largest product fraction. The yield improved from 3.6% without a catalyst to 68.0% with a catalyst. The total lignin product yield was lower without a catalyst (16.0%) than with a catalyst (76.0%). There were substantial differences between the carbon distributions from the commercial alloy catalyst, supported transition metal phosphide catalyst, and catalyst-free processes. This may be due to differences between reaction pathways. Lab-made catalysts cracked the biomass to produce more gases than the alloy catalyst. The final pressure rose from 2 bar at the start of the experiment to 146.15 bar and 46.50 bar after the respective reactions. The particle size, solvent type, time, temperature, gas, and catalytic loading conditions were 180 µm, methanol, 6 h, 300 °C, nitrogen, and 5 wt %, respectively. The results from this study provide a deep understanding of the role of different process parameters, the positive attributes of the direct conversion method, and viability of date palm waste as a potential lignocellulose for production of high-value chemicals.

Highlights

  • The increasing need for more renewable and sustainable fuels and high-value chemicals has motivated researchers to incorporate biomass-based feedstocks into the conventional petroleum-based infrastructure

  • Lignin accounts for approximately 15–40% of the lignocellulose biomass by dry weight and energy, and has the potential to produce sustainable, renewable high-value chemical phenolic platforms and fuels [14,15,16,17]

  • Based on the information reported above, this paper reports production of high-value chemicals from a lignocellulose waste material via catalytic depolymerization process

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Summary

Introduction

The increasing need for more renewable and sustainable fuels (liquid, solid, and gas) and high-value chemicals has motivated researchers to incorporate biomass-based feedstocks into the conventional petroleum-based infrastructure. Lignocellulosic biomass is a promising future raw material for fuels and high-value chemicals due to its carbohydrate (cellulose and hemicellulose) and lignin constituents [6,7]. Lignin is an aromatic polymer that consists of methoxylated phenyl propane units comprising three basic monolignols (sinapyl, coniferyl, and p-coumaryl alcohols). Lignin accounts for approximately 15–40% of the lignocellulose biomass by dry weight and energy, and has the potential to produce sustainable, renewable high-value chemical phenolic platforms and fuels [14,15,16,17]. The above challenges limit the rapid development of lignin but offer many opportunities for further research designed to advance knowledge of lignin depolymerization and increase biorefinery competitiveness

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