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Turning Waste into Value: Comparative Synthesis of Activated Carbon from Non-Recyclable Polystyrene, Corn Stalks and Coffee Grounds
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Researchers synthesized high-surface-area activated carbon from two distinct waste feedstocks—coffee grounds and non-recyclable polystyrene mixed with corn stalks—finding comparable BET surface areas (~914–976 m²/g) despite different processing routes, demonstrating viable pathways for converting diverse waste materials into high-performance adsorbents.
This study investigates the synthesis of activated carbon (AC) from two distinct waste derived feed stocks: coffee grounds (CG) and a mixture of non-recyclable polystyrene (PS) with corn stalks (CS) for the first time. The results of study show that the CG precursor applied the hydrothermal carbonization (HTC) at 240 °C for 5 h followed by KOH activation at 650°C, while the PS–CS mixture was subjected to pyrolysis at 500 °C for 1.5 h and activated at 750 °C. Interestingly, despite the milder treatment conditions, CGderived carbon achieved a good BET surface area of 914.83 m² g⁻¹, comparable to that of PS–CS-derived carbon (976.34 m² g⁻¹). The superior pore development in the CG sample is attributed to its high oxygen and nitrogen content, which facilitates dehydration, decarboxylation, and the formation of micropores during HTC. In contrast, PS requires higher activation temperature due to its aromatic and oxygen-deficient nature, although copyrolysis with CS promotes synergistic gas evolution and pore widening. These findings highlight that feed stock composition strongly dictates process parameters and pore characteristics, providing insights for designing sustainable routes to produce high performance activated carbon from diverse waste materials.
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Converting Polystyrene and Corn Waste into Activated Carbon with High Surface Area
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Researchers converted polystyrene plastic waste and corn stover into high-performance activated carbon through co-pyrolysis followed by KOH chemical activation, achieving a remarkable surface area of 914.83 m²/g — making waste plastics a viable feedstock for advanced materials used in energy storage and environmental remediation.
Co-pyrolysis of spent coffee grounds with carbonates towards activated biochars for wastewater treatment
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Researchers produced activated biochars from spent coffee grounds using carbonate salts (including egg and mussel shell-derived calcium carbonate) via co-pyrolysis, finding that the resulting materials effectively adsorbed water pollutants including pharmaceuticals, dyes, and bisphenol-A, offering a sustainable alternative to conventional activated carbon for wastewater treatment.
Synergistic co-pyrolysis of spent coffee grounds and polypropylene into hydrocarbon-rich bio-oil and carbon-rich biochar
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Researchers co-pyrolyzed spent coffee grounds with polypropylene plastic waste and found that a 50:50 blend maximizes bio-oil yield at 56 wt% with enhanced hydrocarbon content and heating value, while also producing biochar with improved surface area suitable for soil remediation — demonstrating a viable waste-to-energy pathway for two common waste streams.
Trends and Perspectives Towards Activated Carbon and Activated Carbon-derived Materials in Environmental Catalysis Applications
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This review examines trends and emerging applications of activated carbon and activated carbon-derived materials in environmental catalysis, highlighting their chemical stability, high surface area, and porosity as properties that make them effective in remediation and degradation processes.
Valorization of plastic waste via chemical activation and carbonization into activated carbon for functional material applications
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This review examines how waste plastics can be transformed into activated carbon through chemical activation and carbonization processes. Researchers analyzed various methods for converting different plastic types into porous carbon materials with practical applications. The findings suggest that turning plastic waste into activated carbon offers a valuable alternative to traditional disposal methods.
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