Biomass-plastic Co-pyrolysis for sustainable biochar: Mechanisms, reactor technologies, and circular-carbon applications

The rapid accumulation of lignocellulosic biomass residues and plastic waste poses significant environmental challenges because conventional disposal methods, including landfilling and incineration, contribute to greenhouse gas emissions and inefficient resource use. Biochar production through thermochemical conversion offers a potential pathway for valorizing waste streams within a circular carbon framework. This review critically synthesizes recent developments in biomass–plastic co-pyrolysis, focusing on the reaction mechanisms, feedstock interactions, reactor technologies, product characteristics, and life cycle assessment (LCA). It integrates physicochemical and environmental perspectives to address the gap between laboratory-scale co-pyrolysis research and system-level sustainability assessment. It examines multiple parameters, pyrolysis pathways, and feedstock compositions in relation to the biochar yield, carbon sequestration potential, and functional properties. Evidence shows that lignocellulosic biomass, composed of 40–50% cellulose and up to 30% lignin, provides stable carbon matrices, whereas plastic-derived feedstocks, dominated by polyolefins, enhance hydrogen availability and modify thermal degradation pathways. Synergistic co-pyrolysis interactions have been consistently reported to improve carbon stability and tailor porosity, although the product distribution remains highly sensitive to temperature (350–600 °C), residence time, and feedstock ratios. A national-scale assessment has estimated a mitigation potential of up to ∼0.92 Gt CO 2 year −1 for biochar deployment in China under sustainable scenarios. However, bottlenecks pertaining to system boundaries, feedstock heterogeneity, and long-term environmental impact require further assessment. Biomass–plastic co-pyrolysis is a promising circular-carbon pathway, but its scale-up requires feedstock and product standardization, pilot-scale validation, and more consistent environmental assessment.

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Journal
Biomass and Bioenergy
Published
2026-10-14
DOI
https://doi.org/10.1016/j.biombioe.2026.110193
Primary Topic
Thermochemical Biomass Conversion Processes
Type
article
Field-Weighted Citation Impact
0.00

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article

Biomass-plastic Co-pyrolysis for sustainable biochar: Mechanisms, reactor technologies, and circular-carbon applications

Sanjay Basumatary, Andrew Nosakhare Amenaghawon, Noureddine El Messaoudi, Motasem Y.D. Alazaiza et al.
Biomass and Bioenergy
Thermochemical Biomass Conversion Processes
article

Biomass-plastic Co-pyrolysis for sustainable biochar: Mechanisms, reactor technologies, and circular-carbon applications

Sanjay Basumatary, Andrew Nosakhare Amenaghawon, Noureddine El Messaoudi, Motasem Y.D. Alazaiza, Hemamalini Rawindran, Obie Farobie, Amrullah Apip, Jingang Yao, Ramesh T. Subramaniam
article en

Abstract

The rapid accumulation of lignocellulosic biomass residues and plastic waste poses significant environmental challenges because conventional disposal methods, including landfilling and incineration, contribute to greenhouse gas emissions and inefficient resource use. Biochar production through thermochemical conversion offers a potential pathway for valorizing waste streams within a circular carbon framework. This review critically synthesizes recent developments in biomass–plastic co-pyrolysis, focusing on the reaction mechanisms, feedstock interactions, reactor technologies, product characteristics, and life cycle assessment (LCA). It integrates physicochemical and environmental perspectives to address the gap between laboratory-scale co-pyrolysis research and system-level sustainability assessment. It examines multiple parameters, pyrolysis pathways, and feedstock compositions in relation to the biochar yield, carbon sequestration potential, and functional properties. Evidence shows that lignocellulosic biomass, composed of 40–50% cellulose and up to 30% lignin, provides stable carbon matrices, whereas plastic-derived feedstocks, dominated by polyolefins, enhance hydrogen availability and modify thermal degradation pathways. Synergistic co-pyrolysis interactions have been consistently reported to improve carbon stability and tailor porosity, although the product distribution remains highly sensitive to temperature (350–600 °C), residence time, and feedstock ratios. A national-scale assessment has estimated a mitigation potential of up to ∼0.92 Gt CO 2 year −1 for biochar deployment in China under sustainable scenarios. However, bottlenecks pertaining to system boundaries, feedstock heterogeneity, and long-term environmental impact require further assessment. Biomass–plastic co-pyrolysis is a promising circular-carbon pathway, but its scale-up requires feedstock and product standardization, pilot-scale validation, and more consistent environmental assessment.

Biomass and BioenergyVol. 217
Shandong University of Technology (CN), IPB University (ID), Bodoland University (IN), University of Malaya (MY), Lambung Mangkurat University (ID), A'Sharqiyah University, University of Benin (NG)
Kementerian Pendidikan dan Kebudayaan
Responsible consumption and production, Climate action, Affordable and clean energy
Openalex Percentile: Top 25%
Thermochemical Biomass Conversion Processes
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