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    Effect of Acid–Base Pretreatment on Pyrolysis Kinetics of Pine

    Source: Journal of Energy Resources Technology, Part A: Sustainable and Renewable Energy:;2025:;volume( 001 ):;issue: 004::page 41901-1
    Author:
    Geng, Jingjuan
    ,
    Wang, Yang
    ,
    Li, Jinhu
    ,
    Li, Yilong
    ,
    Ye, Xinhao
    ,
    Yang, Yongliang
    DOI: 10.1115/1.4067543
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Biomass represents a significant renewable energy source. Pyrolysis is one method to directly convert biomass into thermochemical energy, with alkali and alkaline earth metals (AAEMs) content potentially improving energy efficiency. In this paper, thermogravimetric experiments were carried out on the samples after acid–base pretreatment, and the kinetics were analyzed using the Friedman, Flynn–Wall–Ozawa, Kissinger–Akahira–Sunose (KAS), and Kissinger methods at various heating rates. The results show that the KAS method is the most reliable among the four methods. As the conversion rate rose from 0.05 to 0.7, the activation energy of water, acid, alkali, and alkaline acid-treated samples calculated using the KAS method increased by 66.08, 42.20, 88.30, and 52.93 kJ/mol, respectively. Acid treatment can remove AAEMs from biomass, inhibit their initial decomposition, and enhance their subsequent decomposition. Alkali treatment can increase the carboxylate content, resulting in a lower activation energy. Nonetheless, the continuous increase in activation energy due to the breaking and reformation of Char–Na bonds hinders subsequent pyrolysis. Additionally, acid–base treatment alters the structure of biomass, leading to a general decrease in activation energy and facilitating its decomposition.
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      Effect of Acid–Base Pretreatment on Pyrolysis Kinetics of Pine

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    contributor authorGeng, Jingjuan
    contributor authorWang, Yang
    contributor authorLi, Jinhu
    contributor authorLi, Yilong
    contributor authorYe, Xinhao
    contributor authorYang, Yongliang
    date accessioned2025-04-21T09:58:55Z
    date available2025-04-21T09:58:55Z
    date copyright1/20/2025 12:00:00 AM
    date issued2025
    identifier issn2997-0253
    identifier otherjerta_1_4_041901.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4305239
    description abstractBiomass represents a significant renewable energy source. Pyrolysis is one method to directly convert biomass into thermochemical energy, with alkali and alkaline earth metals (AAEMs) content potentially improving energy efficiency. In this paper, thermogravimetric experiments were carried out on the samples after acid–base pretreatment, and the kinetics were analyzed using the Friedman, Flynn–Wall–Ozawa, Kissinger–Akahira–Sunose (KAS), and Kissinger methods at various heating rates. The results show that the KAS method is the most reliable among the four methods. As the conversion rate rose from 0.05 to 0.7, the activation energy of water, acid, alkali, and alkaline acid-treated samples calculated using the KAS method increased by 66.08, 42.20, 88.30, and 52.93 kJ/mol, respectively. Acid treatment can remove AAEMs from biomass, inhibit their initial decomposition, and enhance their subsequent decomposition. Alkali treatment can increase the carboxylate content, resulting in a lower activation energy. Nonetheless, the continuous increase in activation energy due to the breaking and reformation of Char–Na bonds hinders subsequent pyrolysis. Additionally, acid–base treatment alters the structure of biomass, leading to a general decrease in activation energy and facilitating its decomposition.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleEffect of Acid–Base Pretreatment on Pyrolysis Kinetics of Pine
    typeJournal Paper
    journal volume1
    journal issue4
    journal titleJournal of Energy Resources Technology, Part A: Sustainable and Renewable Energy
    identifier doi10.1115/1.4067543
    journal fristpage41901-1
    journal lastpage41901-13
    page13
    treeJournal of Energy Resources Technology, Part A: Sustainable and Renewable Energy:;2025:;volume( 001 ):;issue: 004
    contenttypeFulltext
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