4.6 Article

Study on the Staged and Direct Fast Pyrolysis Behavior of Waste Pine Sawdust Using High Heating Rate TG-FTIR and Py-GC/MS

期刊

ACS OMEGA
卷 7, 期 5, 页码 -

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c05907

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资金

  1. National Natural Science Foundation of China [22078363, 21706287]
  2. Fundamental Research Funds for the Central Universities [20CX02208A]
  3. Development Fund of State Key Laboratory of Heavy Oil Processing

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This study used high heating rate thermogravimetry-Fourier transform infrared (TG-FTIR) and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) to investigate the fast pyrolysis kinetics and product evolution of waste pine sawdust. The apparent activation energy for fast pyrolysis was found to be much higher than that of slow pyrolysis, and the release of CO2 was the major deoxygenation route. Cracking mainly occurred at the 450 degrees C stage with phenols, ketones, aldehydes, and sugars as the main products. Furthermore, the selectivity of different compounds varied with pyrolysis temperature.
To understand the fast pyrolysis kinetics and product evolution of waste pine sawdust, high heating rate thermogravimetry-Fourier transform infrared (TG-FTIR) was used to obtain the kinetic parameters and the chemical groups formed during the pyrolysis process, while pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) was used to investigate the detailed compositions of products under the staged (seven stages from 300 to 600 degrees C) and direct fast pyrolysis process. Spectral bands were identified for acids, alcohols, aldehydes, aromatics, esters, ethers, hydrocarbons, ketones, phenols, and sugars. Research found that the apparent activation energy for fast pyrolysis is much higher than that of slow pyrolysis. The evolution of CO2 is the major deoxygenation route. Cracking mainly occurred at the 450 degrees C stage with phenols, ketones, aldehydes, and sugars as the main products. The product distributions for different stages are significantly different; the selectivity of aldehydes decreased, while phenols showed an upward trend with an increase in pyrolysis temperature. Ketones and sugars reached their peak values at 450 degrees C. The changes in the molecular composition of each stage helped to understand the pyrolysis process. Compared with the staged pyrolysis, the direct pyrolysis process had higher selectivity of acids, aldehydes, esters, and sugars and lower selectivity of phenols, ketones, and alcohols.

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