Eiad-Ua, Apiluck
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Eiad-Ua, Apiluck
Alternative Name
Eiad-ua, Apiluck
Eiad-Ua, A.
Eiadua, A.
Main Affiliation
Email
apiluck.ei@kmitl.ac.th
56 results
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Item type:Publication, Catalytic Hydrotreating of Crude Pongamia pinnata Oil to Bio-Hydrogenated Diesel over Sulfided NiMo Catalyst(2022-02-01) ;Plaola, Yuwadee ;Leangsiri, Wanwipa ;Pongsiriyakul, Kanokthip ;Kiatkittipong, WoraponSrifa, AtthaponThis work studied the catalytic activity and stability of Ni-MoS2 supported on γ-Al2O3, SiO2, and TiO2 toward deoxygenation of different feedstocks, i.e., crude Pongamia pinnata oil (PPO) and refined palm olein (RPO). PPO was used as a renewable feedstock for bio-hydrogenated diesel production via catalytic hydrotreating under a temperature of 330 °C, H2 pressure of 50 bar, WHSV of 1.5 h<sup>−1</sup>, and H2/oil (v/v) of 1000 cm<sup>3</sup>/cm<sup>3</sup> under continuous operation. The oil yield from a Soxhlet extraction of PPO was up to 26 wt.% on a dry basis, mainly consisting of C18 fatty acids. The catalytic activity in terms of conversion and diesel yield was in the same trend as increasing in the order of NiMo/γ-Al2O3 > NiMo/TiO2 > NiMo/SiO2. The hydrodeoxygenation (HDO) activity was more favorable over the sulfided NiMo supported on γ-Al2O3 and TiO2, while a high DCO was observed over the sulfided NiMo/SiO2 catalyst, which related to the properties of the support material and the intensity of metal–support interaction. The deactivation of NiMo/SiO2 and NiMo/TiO2 occurred in a short period, due to the phosphorus and alkali impurities in PPO which were not found in the case of RPO. NiMo/γ-Al2O3 exhibited the high resistance of impure feedstock with excellent stabil-ity. This indicates that the catalytic performance is influenced by the purity of the feedstock as well as the characteristics of the catalysts. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, A novel photocatalyst of Y2O3-BaO-ZnO ternary system for enhanced photocatalytic degradation of carbofuran insecticide(2024-08-01) ;Sujinnapram, Supphadate ;Krobthong, Sucheewan ;Moungsrijun, Sasimonton ;Boonruang, ChatdanaiKaewtrakulchai, NapatA novel Y<inf>2</inf>O<inf>3</inf>-BaO-ZnO ternary system was synthesized via precipitation of a mixture of Y(NO<inf>3</inf>)<inf>3</inf>.6 H<inf>2</inf>O:Ba(NO<inf>3</inf>)<inf>2</inf>:Zn(NO<inf>3</inf>)<inf>2</inf>.6 H<inf>2</inf>O using some Fibonacci sequences. The Y<inf>2</inf>O<inf>3</inf>-BaO-ZnO was applied to the photocatalyst to investigate the degradation of carbofuran insecticide. The Y<inf>2</inf>O<inf>3</inf>-BaO-ZnO prepared at the sequence ratio of 5:8:13 (YBZ5) exhibited the highest photocatalytic performance. Morphological characterization showed that the particle size of the YBZ5 sample was significantly smaller than that of ZnO by over half, possibly providing high surface areas. The crystalline structure, functional group, and surface chemical composition investigations confirmed the presence of Y<inf>2</inf>O<inf>3</inf>, BaO, and ZnO. The fluorescence study exhibited no difference. Based on band gap energy and energy band alignment analysis, the Y<inf>2</inf>O<inf>3</inf>-BaO-ZnO ternary system demonstrated a well-aligned valence band. The energy band alignment analysis revealed a good alignment of the valence band for continuous hole transport in the Y<inf>2</inf>O<inf>3</inf>-BaO-ZnO ternary system. The alignment induces charge separation which reduces recombination and provides efficient active carriers at the surfaces of the photocatalyst, allowing reactions with toxic molecules. Therefore, the synergistic function of high surface areas and appropriate energy band alignments of the novel Y<inf>2</inf>O<inf>3</inf>-BaO-ZnO ternary system is considered the crucial factor in the enhancement of photocatalytic performance. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Solid shrimp waste derived nanoporous carbon as an alternative bio-sorbent for oxytetracycline removal from aquaculture wastewater(2024-06-15) ;Kaewtrakulchai, Napat ;Samattakarn, Nippit ;Chanpee, Sirayu; Manatura, KanitRecently, 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 m<sup>2</sup>/g with the total pore volume of 0.458 cm<sup>3</sup>/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. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Novel magnetically interconnected micro/macroporous structure of monolithic porous carbon adsorbent derived from sodium alginate and wasted black liquor and its adsorption performance(2021-01-01) ;Onsri, Parichart ;Dechtrirat, Decha ;Nooeaid, Patcharakamon; Amornpitoksuk, PongsatonThe novel and facile preparation of magnetically interconnected micro/macroporous structure of monolithic porous carbon adsorbent (MPCA) were designed and presented herein. The synthesis was achieved via conventional freeze-drying and pyrolysis processes. In this study, sodium alginate and wasted black liquor were employed as starting pre-cursors. Sodium alginate acts as a template of materials, whereas black liquor, the wasted product from the paper industry with plentiful of lignin content and alkaline solution, played an essential role in the reinforcement and activation of porosity for the resulting materials. Moreover, both the precursors were well dissolved in Fe<sup>3+</sup> solution, providing a simple addition of a magnetic source in a one-pot synthesis. The interconnected micro/macroporous structures were generated through freeze-drying and, subsequently the pyrolysis process. The obtained cylindrical-shaped monolithic porous carbon adsorbent (MPCA-700) showed high mechanical stability, a high BET specific surface area (902 m<sup>2</sup>/g). Such aforementioned features were considered suitable to make the synthesized monolith as an adsorbent for the removal of heavy metal ions. The maximum adsorption capacity of MPCA-700 towards Pb<sup>2+</sup> ions was 76.34 mg/g at pH 5. The adsorption studies illustrated that adsorption kinetics and isotherm perfectly fitted with the pseudo-second-order kinetics model and Langmuir isotherm, respectively. This work presents a promising pro-tocol to reduce the overall costs in the preparation of renewable adsorbents with good adsorption efficiency and regeneration. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Palm oil conversion to bio-jet and green diesel fuels over cobalt phosphide on porous carbons derived from palm male flowers(2020-06-01) ;Kaewtrakulchai, Napat ;Kaewmeesri, Rungnapa ;Itthibenchapong, Vorranutch; Faungnawakij, KajornsakPorous carbon was successfully synthesized from palm male flowers (PMFs), using microwave-assisted potassium hydroxide (KOH) activation and was used as a catalyst support for the conversion of palm oil into bio-hydrocarbons, in fractions of green diesel and bio-jet fuel. Palm male flower-derived porous carbon (PC), consolidated with well dispersed cobalt phosphide (CoP) nanoparticles, was synthesized by simple wet-impregnation with subsequent thermal treatment. The physicochemical properties of the synthesized CoP/PC catalysts were evaluated by various techniques including proximate and ultimate elemental analysis, FTIR, XRD, N<inf>2</inf> sorption, SEM, TEM–EDS, and NH<inf>3</inf>-temperature programmed desorption (TPD). The effects of the pyrolysis temperatures (600−900<sup>◦</sup> C), used for the impregnated samples before the reduction process, on catalyst properties and catalytic performance were investigated. Moreover, the effect of a liquid hourly space velocity of 0.5–1.5 h<sup>−1</sup> and reaction temperatures of 340–420<sup>◦</sup> C was studied in the palm oil conversion. The catalyst pyrolyzed at 600<sup>◦</sup> C possessed the greatest particle dispersion and surface area, and showed the highest yield of liquid hydrocarbon product (C9–C18). We also found that the high pyrolysis temperature above 800<sup>◦</sup> C partially transformed the Co<inf>2</inf> P phase into CoP one which significantly exhibited higher cracking activity and bio-jet selectivity, due to the improved acidity of the catalyst. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Fundamental study of carbon materials derived from empty fruit bunch via hydrothermal carbonization(2018-11-01) ;Guntagerng, Kanogpan ;Panomsuwan, GasiditThe utilization of biomass has recently gained great attention in recent years owing to growth of global environmental concerns. The aim of this work is to study the morphology of carbon materials derived from biomass oil palm empty fruit bunch (EFB) via hydrothermal carbonization (HTC) at different temperatures (160-200 °C) and times (4-12 h) followed by carbonization at 300-900 °C under nitrogen atmosphere for 2 h. The physiochemical properties of carbon sample were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy and surface area analysis. The results demonstrated that the increase of hydrothermal temperature, hydrothermal time, and carbonization temperature resulted in the formation of carbon materials with higher surface area, porosity and carbon content. Our results revealed that carbon derived from EFB via HTC at optimal condition exhibited porous structure with high surface area, which can be further applied for absorbent applications. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, 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; 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. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Effect of sr substitution on structural, ferroelectric and magnetic properties of la1-xsrxfeo3 perovskite oxides(2020-01-01) ;Kaewpanha, Malinee ;Nunocha, Pornnipa ;Bongkarn, Theerachai; Suriwong, TawatEffect of Sr substitution on structural, magnetic and electrical properties of LaFeO<inf>3</inf> perovskite oxides has been studied. Using the selected Sr doping content (x) from 0.0 to 1.0, perovskite La<inf>1-x</inf>Sr<inf>x</inf>FeO<inf>3</inf> nanopowder was synthesized by sol-gel auto-combustion method, followed by calcination at 900 °C for 2 h. The synthesized powder was pressed into disks at room temperature and then the disk samples were sintered at 1200 °C for 12 h to obtain a single-phase compound formation and uniaxial compaction. The influence of Sr doping on the phase formation, morphology, ferroelectric and magnetic properties was investigated. The phase formation of the sample changes from orthorhombic at low Sr doping through rhombohedral to cubic for Sr-rich sample as the stoichiometry approached SrFeO<inf>3</inf>. The grains of La<inf>1-x</inf>Sr<inf>x</inf>FeO<inf>3</inf> ceramics revealed an irregular polyhedron shape. SEM-EDS mapping analysis also exhibited the uniform distribution of all elements. The direct energy gap (E<inf>g</inf>) was found to decrease with increasing amounts of Sr doping. Moreover, the La<inf>0.6</inf>Sr<inf>0.4</inf>FeO<inf>3</inf> ceramic exhibited ferromagnetic behavior with saturated magnetization (M<inf>s</inf>) of 0.305 emu/g at room temperature. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, High performance nanoporous carbon from mulberry leaves (Morus alba L.) residues via microwave treatment assisted hydrothermal-carbonization for methyl orange adsorption: Kinetic, equilibrium and thermodynamic studies(2022-03-01) ;Siraorarnroj, Siwat ;Kaewtrakulchai, Napat ;Fuji, MasayoshiHigh performance nanoporous carbons were directly prepared from mulberry leaves (Morus alba L.) residues by the hydrothermal-carbonization with chemical reagent combined the microwave-assisted treatment. The as-purified ML porous carbon (MPC) was successfully applied for the adsorption of methyl orange, which is one of crucial waste-water pollutants left from an industrial sector. The MPC sample obtained from the hydrothermal process (200 °C, 12 h) using an activation of 15 wt% NaOH (700 °C, 2 h), and combined with microwave treatment at 700 W for 6 min, specifically exhibited micropores and mesopores in the MPC morphological structure. Accordingly, the highest S<inf>BET</inf> was approximately 791.79 m<sup>2</sup>/g with the total pore volume of 0.495 cm<sup>3</sup>/g. Moreover, the adsorption performance test of MPC was conducted by the shaking unit using 100 ppm methyl orange concentration. The MPC showed the highest methyl orange-adsorption uptake of 99% at 30 °C under an ambient pressure (1 atm). The development of mulberry leaves (Morus alba L.) residues into porous carbon exhibited a great attention for dyes adsorption with a rapid adsorption kinetic, and excellent adsorption capacity, which are a promising-characteristics for practical waste-water adsorption experiments. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Simultaneous production of hydrogen and carbon nanotubes from biogas: On the design of combined process(2022-04-15) ;Rattanaamonkulchai, Raminda ;Kludpantanapan, Thunyathon ;Nantapong, Paveenuch ;Srifa, AtthaponKoo-Amornpattana, WanidaWe introduced a novel combined process of CO<inf>2</inf> methanation (METH) and catalytic decomposition of methane (CDM) for simultaneous production of hydrogen (H<inf>2</inf>) and carbon nanotubes (CNTs) from biogas. In this process, biogas is catalytically upgraded into CH<inf>4</inf>-rich gas in METH reactor using Ni/CeO<inf>2</inf> catalyst, and the obtained CH<inf>4</inf>-rich gas is subsequently decomposed into H<inf>2</inf> and CNTs in CDM reactor over CoMo/MgO catalyst. Among the three different process scenarios proposed, the combined process with a steam condenser equipped between METH and CDM reactors could greatly improve a CNTs productivity. The CNTs production yield increased by more than 2.5-fold, maximizing at 9.08 gCNTs/gCat with a CNTs purity of 90%. The deposited carbon product was characterized as multi-walled carbon nanotubes (MWCNTs) with a surface area of 136.0 m<sup>2</sup>/g, comparable with commercial CNTs of 199.8 m<sup>2</sup>/g. The remarkable I<inf>G</inf>/I<inf>D</inf> ratio of 2.18 confirms a superior portion of graphitic carbon in the synthesized CNTs upon the commercial CNTs with I<inf>G</inf>/I<inf>D</inf> = 0.74. Notably, the CH<inf>4</inf> conversion reached 94.5%, while the CO<inf>2</inf> conversion achieved 100%, resulting in the H<inf>2</inf> yield and H<inf>2</inf> purity higher than 90%. This combined process demonstrates a promising route for production of high quality CNTs and high purity H<inf>2</inf> with complete CO<inf>2</inf> conversion using biogas as abundant renewable energy resources. In addition, the test of raw biogas showed no deactivation of catalyst, justifying the implementation of the developed process for real biogas without purification.
