Investigating the synergy of fast co-pyrolysis of spent coffee ground and disposed urban facemask: analysis of kinetics and product compositions

• Co-pyrolysis of spent coffee grounds and facemasks was investigated • Fraser–Suzuki deconvolution revealed four peaks in co-pyrolysis DTG • Model-free methods effectively estimated kinetic parameters • Co-pyrolysis synergy enhanced during the second decomposition stage • Co-pyrolysis reduced acids and oxygenates in pyrolysis vapors This study investigates the thermo-kinetic behavior and product distribution during the co-pyrolysis of spent coffee grounds (SCG) and facemasks (FM). TGA was employed to evaluate the kinetics and thermodynamics of the pyrolysis process by segmenting the thermal decomposition into stage I (200 – 360°C) and stage II (360 – 550°C), while Py-GC/MS was used to analyse the product composition. SCG and FM blends with varying ratios by wt.% (SCG:FM = 100:0, 75:25, 50:50, 25:100, and 0:100) were subjected to pyrolysis at four heating rates (5, 10, and 30°C/min). The decomposition curves were deconvoluted using Fraser-Suzuki deconvolution method into four peaks related to biomass pseudo-components and FM degradation. The deconvoluted curves showed potential synergistic interaction at the lignin and FM decomposition zone (460 – 500°C). The kinetic analyses were carried out using three model-free methods to investigate the activation energy ( Ea ) and thermodynamics of co-pyrolysis. The lowest Ea value was obtained at SCG25%FM%75% (305.1 – 239 kJ/mol), mostly pronounced in stage II. Py-GC/MS analysis of the co-pyrolysis products demonstrates that the decomposition of polypropylene polymer of the FM promoted the formation of aliphatic hydrocarbons and reduces the overall acidity. This effect was further amplified at higher pyrolysis temperatures (450 – 650°C). The blending ratio also plays a significant role, with a higher polymer content (SCG25%FM75%) leading to a more aliphatic products and a significant decline in carboxylic acids and anhydro-sugars. Moreover, co-pyrolysis reduced the N containing compounds significantly. Finally, policy implications and recommendations for co-pyrolysis adoption were incorporated. Overall, this study highlights the potential of utilizing waste material like SCG and FM for the sustainable production of valuable chemicals and fuels.

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Publication Details

Journal
Environmental Challenges
Published
2025-10-09
DOI
https://doi.org/10.1016/j.envc.2025.101344
Citations
1
Primary Topic
Thermochemical Biomass Conversion Processes
Type
article
Field-Weighted Citation Impact
0.67
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article

Investigating the synergy of fast co-pyrolysis of spent coffee ground and disposed urban facemask: analysis of kinetics and product compositions

Jurarat Nisamaneenate, Viboon Sricharoenchaikul, Duangduen Atong, Prangtip Rittichote Kaewpengkrow et al.
1 citations
Environmental Challenges
Thermochemical Biomass Conversion Processes
0.67
article

Investigating the synergy of fast co-pyrolysis of spent coffee ground and disposed urban facemask: analysis of kinetics and product compositions

Jurarat Nisamaneenate, Viboon Sricharoenchaikul, Duangduen Atong, Prangtip Rittichote Kaewpengkrow, Imad A. Idris
article en
1 citations

Abstract

• Co-pyrolysis of spent coffee grounds and facemasks was investigated • Fraser–Suzuki deconvolution revealed four peaks in co-pyrolysis DTG • Model-free methods effectively estimated kinetic parameters • Co-pyrolysis synergy enhanced during the second decomposition stage • Co-pyrolysis reduced acids and oxygenates in pyrolysis vapors This study investigates the thermo-kinetic behavior and product distribution during the co-pyrolysis of spent coffee grounds (SCG) and facemasks (FM). TGA was employed to evaluate the kinetics and thermodynamics of the pyrolysis process by segmenting the thermal decomposition into stage I (200 – 360°C) and stage II (360 – 550°C), while Py-GC/MS was used to analyse the product composition. SCG and FM blends with varying ratios by wt.% (SCG:FM = 100:0, 75:25, 50:50, 25:100, and 0:100) were subjected to pyrolysis at four heating rates (5, 10, and 30°C/min). The decomposition curves were deconvoluted using Fraser-Suzuki deconvolution method into four peaks related to biomass pseudo-components and FM degradation. The deconvoluted curves showed potential synergistic interaction at the lignin and FM decomposition zone (460 – 500°C). The kinetic analyses were carried out using three model-free methods to investigate the activation energy ( Ea ) and thermodynamics of co-pyrolysis. The lowest Ea value was obtained at SCG25%FM%75% (305.1 – 239 kJ/mol), mostly pronounced in stage II. Py-GC/MS analysis of the co-pyrolysis products demonstrates that the decomposition of polypropylene polymer of the FM promoted the formation of aliphatic hydrocarbons and reduces the overall acidity. This effect was further amplified at higher pyrolysis temperatures (450 – 650°C). The blending ratio also plays a significant role, with a higher polymer content (SCG25%FM75%) leading to a more aliphatic products and a significant decline in carboxylic acids and anhydro-sugars. Moreover, co-pyrolysis reduced the N containing compounds significantly. Finally, policy implications and recommendations for co-pyrolysis adoption were incorporated. Overall, this study highlights the potential of utilizing waste material like SCG and FM for the sustainable production of valuable chemicals and fuels.

Environmental ChallengesVol. 21
Chulalongkorn University (TH), Thailand National Metal and Materials Technology Center (TH), King Mongkut's Institute of Technology Ladkrabang (TH)
Openalex Percentile: Top 26%
Thermochemical Biomass Conversion Processes
0.67
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