Non-isothermal thermal decomposition behavior and reaction kinetics of acrylonitrile butadiene styrene (ABS)

Environmental concerns associated with the rapid rising plastic consumption have led to the search for better waste utilization and management. Pyrolysis has emerged as an ideal and promising waste management technique for energy extraction from plastic waste. The aim of this work is to explore the...

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Veröffentlicht in:Journal of environmental management 2023-12, Vol.348, p.119080-119080, Article 119080
Hauptverfasser: Xu, Li, Li, Shengcai, Zhang, Youchao, Sun, Wanghu, Pan, Longwei, Wang, Lei
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container_title Journal of environmental management
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creator Xu, Li
Li, Shengcai
Zhang, Youchao
Sun, Wanghu
Pan, Longwei
Wang, Lei
description Environmental concerns associated with the rapid rising plastic consumption have led to the search for better waste utilization and management. Pyrolysis has emerged as an ideal and promising waste management technique for energy extraction from plastic waste. The aim of this work is to explore the effects of operation temperature and heating rate on the pyrolysis behavior under non-isothermal heating conditions. The decomposition characteristics, reaction mechanism, kinetics and thermodynamics of a typical widely used thermosetting plastic, acrylonitrile butadiene styrene (ABS), were studied via coupled thermogravimetry, Fourier transform infrared spectrometry and gas chromatography-mass spectrometry analysis (TG-FTIR-GC/MS). Kinetic analysis showed the average Eα values are estimated to be 187.02, 188.55, 187.04 and 185.67 kJ/mol via advanced Vyazovkin, Flynn-Wall-Ozawa (FWO), Tang and Starink model-free method, respectively. Model-fitting CR and master-plots methods indicated that f(α)=(1-α)n is the most probable reaction mechanism. The equation of kinetic compensation effect was further developed as lnA = −3.1955 + 0.1736 Eα. Furthermore based on these initial inferences, a new reaction scheme coupled with Particle Swarm Optimization (PSO) was put forward for modeling ABS pyrolysis. The optimized values for E, A and n were 198.07 kJ/mol, 7.61 × 1012 s−1 and 1.56, respectively. The predicted results showed that the experimental data can be well characterized by the optimized parameters from PSO, validating the effectiveness and accuracy of the inverse modeling procedure. Moreover, it is found that the volatile products are mainly composed of aromatic compounds, ketones, amines, esters, nitrile compounds, alkenes and amines. Based on the FT-IR and GC-MS results, the possible chemical reactions for ABS pyrolysis from molecular structure were proposed. Finally, thermodynamic analysis were carried out, the calculated values of enthalpy ΔH, Gibb's free energy ΔG and entropy ΔS indicated that non-spontaneous reactions with low favorability exists during ABS decomposition, the process is complex therefore extra energy is needed to promote the reaction. The above obtained results should offer as an important reference for future disposal and thermochemical management of plastic waste. •ABS pyrolysis kinetics is studied by combined model-free and model-fitting methods.•GC-MS suggested the main volatile products released are aromatic compounds.•n-th order reactio
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Pyrolysis has emerged as an ideal and promising waste management technique for energy extraction from plastic waste. The aim of this work is to explore the effects of operation temperature and heating rate on the pyrolysis behavior under non-isothermal heating conditions. The decomposition characteristics, reaction mechanism, kinetics and thermodynamics of a typical widely used thermosetting plastic, acrylonitrile butadiene styrene (ABS), were studied via coupled thermogravimetry, Fourier transform infrared spectrometry and gas chromatography-mass spectrometry analysis (TG-FTIR-GC/MS). Kinetic analysis showed the average Eα values are estimated to be 187.02, 188.55, 187.04 and 185.67 kJ/mol via advanced Vyazovkin, Flynn-Wall-Ozawa (FWO), Tang and Starink model-free method, respectively. Model-fitting CR and master-plots methods indicated that f(α)=(1-α)n is the most probable reaction mechanism. The equation of kinetic compensation effect was further developed as lnA = −3.1955 + 0.1736 Eα. Furthermore based on these initial inferences, a new reaction scheme coupled with Particle Swarm Optimization (PSO) was put forward for modeling ABS pyrolysis. The optimized values for E, A and n were 198.07 kJ/mol, 7.61 × 1012 s−1 and 1.56, respectively. The predicted results showed that the experimental data can be well characterized by the optimized parameters from PSO, validating the effectiveness and accuracy of the inverse modeling procedure. Moreover, it is found that the volatile products are mainly composed of aromatic compounds, ketones, amines, esters, nitrile compounds, alkenes and amines. Based on the FT-IR and GC-MS results, the possible chemical reactions for ABS pyrolysis from molecular structure were proposed. Finally, thermodynamic analysis were carried out, the calculated values of enthalpy ΔH, Gibb's free energy ΔG and entropy ΔS indicated that non-spontaneous reactions with low favorability exists during ABS decomposition, the process is complex therefore extra energy is needed to promote the reaction. 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Pyrolysis has emerged as an ideal and promising waste management technique for energy extraction from plastic waste. The aim of this work is to explore the effects of operation temperature and heating rate on the pyrolysis behavior under non-isothermal heating conditions. The decomposition characteristics, reaction mechanism, kinetics and thermodynamics of a typical widely used thermosetting plastic, acrylonitrile butadiene styrene (ABS), were studied via coupled thermogravimetry, Fourier transform infrared spectrometry and gas chromatography-mass spectrometry analysis (TG-FTIR-GC/MS). Kinetic analysis showed the average Eα values are estimated to be 187.02, 188.55, 187.04 and 185.67 kJ/mol via advanced Vyazovkin, Flynn-Wall-Ozawa (FWO), Tang and Starink model-free method, respectively. Model-fitting CR and master-plots methods indicated that f(α)=(1-α)n is the most probable reaction mechanism. The equation of kinetic compensation effect was further developed as lnA = −3.1955 + 0.1736 Eα. Furthermore based on these initial inferences, a new reaction scheme coupled with Particle Swarm Optimization (PSO) was put forward for modeling ABS pyrolysis. The optimized values for E, A and n were 198.07 kJ/mol, 7.61 × 1012 s−1 and 1.56, respectively. The predicted results showed that the experimental data can be well characterized by the optimized parameters from PSO, validating the effectiveness and accuracy of the inverse modeling procedure. Moreover, it is found that the volatile products are mainly composed of aromatic compounds, ketones, amines, esters, nitrile compounds, alkenes and amines. Based on the FT-IR and GC-MS results, the possible chemical reactions for ABS pyrolysis from molecular structure were proposed. 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Pyrolysis has emerged as an ideal and promising waste management technique for energy extraction from plastic waste. The aim of this work is to explore the effects of operation temperature and heating rate on the pyrolysis behavior under non-isothermal heating conditions. The decomposition characteristics, reaction mechanism, kinetics and thermodynamics of a typical widely used thermosetting plastic, acrylonitrile butadiene styrene (ABS), were studied via coupled thermogravimetry, Fourier transform infrared spectrometry and gas chromatography-mass spectrometry analysis (TG-FTIR-GC/MS). Kinetic analysis showed the average Eα values are estimated to be 187.02, 188.55, 187.04 and 185.67 kJ/mol via advanced Vyazovkin, Flynn-Wall-Ozawa (FWO), Tang and Starink model-free method, respectively. Model-fitting CR and master-plots methods indicated that f(α)=(1-α)n is the most probable reaction mechanism. The equation of kinetic compensation effect was further developed as lnA = −3.1955 + 0.1736 Eα. Furthermore based on these initial inferences, a new reaction scheme coupled with Particle Swarm Optimization (PSO) was put forward for modeling ABS pyrolysis. The optimized values for E, A and n were 198.07 kJ/mol, 7.61 × 1012 s−1 and 1.56, respectively. The predicted results showed that the experimental data can be well characterized by the optimized parameters from PSO, validating the effectiveness and accuracy of the inverse modeling procedure. Moreover, it is found that the volatile products are mainly composed of aromatic compounds, ketones, amines, esters, nitrile compounds, alkenes and amines. Based on the FT-IR and GC-MS results, the possible chemical reactions for ABS pyrolysis from molecular structure were proposed. Finally, thermodynamic analysis were carried out, the calculated values of enthalpy ΔH, Gibb's free energy ΔG and entropy ΔS indicated that non-spontaneous reactions with low favorability exists during ABS decomposition, the process is complex therefore extra energy is needed to promote the reaction. The above obtained results should offer as an important reference for future disposal and thermochemical management of plastic waste. •ABS pyrolysis kinetics is studied by combined model-free and model-fitting methods.•GC-MS suggested the main volatile products released are aromatic compounds.•n-th order reaction model is identified to best describe ABS pyrolysis mechanism.•Kinetic parameters characterizing the pyrolysis process are optimized by PSO.•Possible chemical reactions pathway for ABS thermal degradation is given.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.jenvman.2023.119080</doi><tpages>1</tpages></addata></record>
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subjects algorithms
alkenes
chemical structure
energy
enthalpy
entropy
equations
Fourier transform infrared spectroscopy
gas chromatography-mass spectrometry
Gibbs free energy
kinetics
Particle swarm optimization
Plastic waste
plastics
pyrolysis
Pyrolysis kinetics
reaction kinetics
Reaction mechanism
reaction mechanisms
styrene
TG-FTIR-GC/MS
thermogravimetry
waste utilization
wastes
title Non-isothermal thermal decomposition behavior and reaction kinetics of acrylonitrile butadiene styrene (ABS)
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