4.7 Article

Effects of K2CO3 on pyrolysis characteristics of Xinjiang cotton stalk

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 48, 期 13, 页码 5069-5079

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.11.051

关键词

Alkali metals; Pyrolysis; Cotton

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The reaction parameters of K in-situ catalytic pyrolysis of cotton stalks at 600 degrees C were examined using the horizontal fixed bed pyrolysis method. The influence of K on the pyrolysis conversion mechanism of cotton stalks was investigated through various analyses. The addition of K2CO3 accelerated the breakdown of oxygen-containing rings, promoted the conversion of furan structure, and prevented the transformation of furan into long-chain alkanes.
The horizontal fixed bed pyrolysis method was used in this study to examine the reaction parameters of K in-situ catalytic pyrolysis of the cotton stalk at 600 degrees C. The pyrolysis conversion mechanism of cotton stalk under the influence of K was investigated in conjunction with gas chromatography analysis, FT-IR analysis, and GC-MS analysis. According to the findings, the gas production of a mixture of 1 g cotton stalks grew from 215 mL (0.0 %- K2CO3) to 275 mL (7.5% -K2CO3), but it was inhibited to 263 mL when K2CO3 addition was at 10.0%. According to the results of the characterization, K2CO3 might accelerate the breakdown of oxygen-containing rings in cellulose and hemicellulose, encourage the conversion of furan structure into ketones, and prevent the transformation of furan into long-chain alkanes. The addition of K2CO3 introduces more K into the cotton stalk. Under the influence of K, long-chain alkanes, phenols, and esters will be further cracked and polymerized to create more stable aromatic hydrocarbons. According to quantum chemical calculations, xylose's oxygen-containing ring opened first without the presence of K, then H transfer, dehydrogenation, dehydration, and cyclization to generate the cyclopentanone structure. The oxygen-containing groups in the xylose side chain preferentially bind to K in the presence of K, and the bond length between the O and C rings of the side chain is lengthened, while without K, the C-O bond length of the preferred ring opening is shortened.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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