4.5 Article

Targeted production of aromatics from corn stover and high-density polyethylene composite pyrolysis over nitric acid modified biochar catalyst

Journal

JOURNAL OF THE ENERGY INSTITUTE
Volume 112, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.joei.2023.101447

Keywords

Biomass; Pyrolysis; Mono-aromatics; Biochar catalyst; Nitric acid modification

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The pore structure and active functional groups of biochar are crucial for its catalytic performance. This study found that modification of coconut shell-derived biochar with nitric acid enhanced its catalytic performance in producing aromatics during the pyrolysis of a corn stover/high-density polyethylene composite. Higher modification temperature, longer treatment time, and lower nitric acid concentration were observed to be effective in increasing the yield of aromatics while reducing the formation of aliphatics and oxygenates. The highest yield of aromatic hydrocarbons was achieved under specific conditions. The nitric acid-modified biochar catalyst also promoted the production of CO and CH4, suggesting enhanced decarbonylation and end-chain breaking reactions.
The pore structure and active functional groups of biochar play a critical role in determining its catalytic performance. In this study, coconut shell-derived biochar underwent modification with nitric acid to serve as a catalyst in the pyrolysis of a corn stover/high-density polyethylene composite (CHC) in a fixed bed reactor. The effects of nitric acid concentration, treatment time, and temperature on the catalytic performance of biochar were investigated, specifically targeting the production of aromatics during the CHC pyrolysis process. The results revealed that a higher modification temperature, a longer treatment time, and a lower concentration of nitric acid effectively enhanced the catalytic performance of biochar in producing aromatics, while simultaneously reducing the formation of aliphatics and oxygenates. The highest yield of aromatic hydrocarbons (56.1 %) was obtained under the conditions of a modification temperature of 90 degrees C, a modification time of 10 h, and a nitric acid concentration of 1.0 mol/L. Furthermore, the nitric acid-modified biochar catalyst promoted the production of CO and CH4 during the CHC pyrolysis process, indicating that the decarbonylation and end-chain breaking reactions were enhanced due to the presence of abundant oxygen-containing functional groups introduced by nitric acid oxidation.

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