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Oil palm leaf-derived nanoporous carbon via hydrothermal carbonization combined with NaOH microwave activation for tetracycline adsorption
(2025-11-01)
Chanpee, Sirayu
;
Apinyakul, Naruemon
;
Kaewtrakulchai, Napat
;
Khemasiri, Narathon
;
Eiad-ua, Apiluck
Generally, the increase in pharmaceutical industrial activities has led to a corresponding rise in water resource contamination. Efforts have been dedicated to addressing the urgent challenge of waste biomass disposal by developing recycling methods capable of producing bio-adsorbents. Adsorption is a promising approach for removing tetracycline contaminants, owing to its simplicity, stability, and cost-effectiveness. In this study, a low-cost activated biochar was successfully developed using oil palm leaf (OPL) via hydrothermal carbonization (HTC) combined microwave-assisted pyrolysis system (MAPS) using sodium hydroxide (NaOH). The HTC and MAPS processes enhanced high mass yield, porosity, energy efficiency, and reduced reaction time. NaOH treatment improved the porosity of the activated biochar derived from OPL, resulting primarily in a mesoporous structure. However, NaOH treatment via the MAPS process increased surface area and porosity. Among the samples tested, OPLC-NaOH-1:1 exhibited the largest surface area and highest porosity, making it the chosen candidate for further TC adsorption tests. The adsorption experiments revealed that the Langmuir isotherm model and the pseudo-second-order kinetic model accurately matched the experimental data, suggesting a mono-layered adsorption mechanism due to micropores and chemisorption interactions. Additionally, thermodynamic analysis indicated an endothermic and spontaneous reaction during the adsorption process. The adsorption of nanoporous carbon for TC was primarily regulated by pore filling, hydrogen bonding, electrostatic effects, and π-π interactions also playing a significant role. Overall, this study highlights the potential of utilizing OPL waste as a sustainable material for producing nanoporous carbon and underscores the effectiveness of nanoporous carbon for adsorbing antibiotics.
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Co-hydrothermal carbonization of polystyrene waste and maize stover combined with KOH activation to develop nanoporous carbon as catalyst support for catalytic hydrotreating of palm oil
(2024-12-01)
Kaewtrakulchai, Napat
;
Chanpee, Sirayu
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Jadsadajerm, Supachai
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Wongrerkdee, Sutthipoj
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Manatura, Kanit
Plastic waste is massively generated daily from households, mainly as packaging material, causing serious surrounding ecological problems. The development of plastic waste for higher value-added applications instead of landfilling and incineration has received consideration interest in bioenergy and material science research. Herein, a nanoporous carbon support of nickel phosphide catalyst for palm oil hydrotreating was developed from blended polystyrene waste and maize stover via the Co-hydrothermal carbonization (HTC) coupled with the KOH activation process. The Co-HTC parameters, such as temperature, reaction time, and PS percentage, were studied on the properties of co-hydrochar feedstocks for further activation using the Box behnken design. From the comprehensive characterization results, response surface methodology (RSM) results showed that the rising polystyrene proportion significantly exhibited the higher production yield and fixed carbon of co-hydrochar products, an essential characteristic for porous carbon manufacturing. After activation step, the final nanoporous carbon derived from the co-hydrochar (PMPC) exhibited the highest specific surface area of 1033.58 m2/g with total pore volume of 0.45 cm3/g. Moreover, the PCMC-supported nickel phosphide catalysts were successfully synthesized and tested for the catalytic hydrotreating of palm oil as alternative catalyst. The NiP-PMPC catalyst represents an impressive liquid hydrocarbon yield of 74.68 % with a high green diesel selectivity of 85.92 % at 100 % palm oil conversion. The findings of this study might help develop and utilize blended plastic waste and agricultural waste as an alternate catalytic support for various processes in biofuel and biochemical synthesis.
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Solid shrimp waste derived nanoporous carbon as an alternative bio-sorbent for oxytetracycline removal from aquaculture wastewater
(2024-06-15)
Kaewtrakulchai, Napat
;
Samattakarn, Nippit
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Chanpee, Sirayu
;
Assawasaengrat, Pornsawan
;
Manatura, Kanit
Recently, it has been critical to effectively remove oxytetracycline (OTC) from aquaculture wastewater before releasing into the environment. The adsorption process is recognized as an efficient pathway for removing OTC since it is a simple, stable, and cost-effective method. This study aims to develop nanoporous carbon entirely from shrimp waste (SW) via hydrothermal carbonization assisted with KOH activation. Existing KOH significantly increases the porosity of SW nanoporous carbon. The optimal SW porous carbon was obtained using 5 wt%KOH for activation, which had the largest surface area of 679.51 m2/g with the total pore volume of 0.458 cm3/g. Moreover, the SW porous carbon with the highest porosity was selected for the OTC adsorption. The Langmuir isotherm model and the pseudo-second-order kinetic model match the experimental data, implying that the adsorption mechanism is mono-layered adsorption due to micropores by chemisorption interaction. The adsorption capacity significantly improved by increasing the dosage of SW nanoporous carbon. The SW nanoporous carbon adsorption for OTC is primarily regulated by pore filling affected by hydrogen bonding, and π-π* interaction also plays a significant role. The SW nanoporous carbon showed an efficient OTC adsorption after 5 regeneration cycles. This work demonstrates biomass waste recycling and emphasizes the potential of aquatic food processing waste-derived nanoporous carbon for antibiotic adsorption.
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Synthesis of nanoporous carbon from brewer waste by hydrothermal carbonization assisted chemical activation for carbamazepine adsorption
(2024-06-01)
Apinyakul, Naruemon
;
Chanpee, Sirayu
;
Kaewtrakulchai, Napat
;
Khemasiri, Narathon
;
Eiad-ua, Apiluck
Nanoporous carbon (NPC) has gained significant attention in wastewater treatment due to its effectiveness. The adsorption process, known for its simplicity, stability, and cost-effectiveness, is widely recognized as an efficient method for removing carbamazepine (CBZ) residues accumulate in the environment. However, the application of NPC is often hindered by challenges in the regeneration process after use, as well as issues related to large surface area, pore size, and functional groups. Fortunately, the samples in this study not only maintained their adsorption efficiency but also demonstrated the ability to be regenerated multiple times. Herein brewery waste was subjected to hydrothermal treatment at 200 °C for 1 h and followed by KOH and NaCl activation with different KOH:NaCl (w/w) ratios of 5:0, 4:1, 3:2, 1:1, 2:3, 1:4, and 0:5 to optimize the properties of malt husk derived nanoporous carbon (NPC). The optimal condition KOH:NaCl ratio of 1:1 had a maximum specific surface area of 906 m2/g with a total pore volume of 0.252 cm3/g. According to the adsorption test, the CBZ adsorption isotherm was well-fitted to the Langmuir model (R2 = 0.976) kinetic data were consistent with the pseudo-second-order model (R2 = 0.995). This suggests that the adsorption mechanism involves monolayer adsorption and chemisorption interaction. The Gibbs free energy and enthalpy of CBZ adsorption by NPC were found to be spontaneous and endothermic. The regeneration test revealed a 95.35% decrease in the adsorption capacity of NPC after 5 repeated cycles. Consequently, the study suggests a potential application of nanoporous carbon from MH as an alternative adsorbent for removing carbamazepine in wastewater.

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