Eiad-Ua, Apiluck

Preferred name

Eiad-Ua, Apiluck

Alternative Name

Eiad-ua, Apiluck

Eiad-Ua, A.

Eiadua, A.

Main Affiliation

Integrated Innovative Technology

apiluck.ei@kmitl.ac.th

Now showing 1 - 10 of 18

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N-doped Porous Carbon from Palm Male Flower via Hydrothermal Carbonization
(2020-07-30)
Verasarut, Panupong
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Liamprawat, Tanatorn
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Kaewtrakulchai, Napat
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Chutipaijit, Sutee
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Panomsuwan, Gasidit
N-doped porous carbon materials were produced from palm male flower using hydrothermal carbonization processes at 200 C for 24 h followed by N-Doping and carbonization at 700C for 2 h. N-doping was carried out by impregnation using NH4OH at 0.5, 1.0, 1.5 M and 2 M. Products were characterized by means of chemical composition and morphology using SEM, XPS, and XRD to characterize specific properties such as physical morpholog, porosity, elemental composition on surface and crystalline structure of PMF. After applying hydrothermal carbonization processes, the results showed substantially increased porosity and surface area with suitable microstructure for N-doped electrodes applications. The highest porosity was obtained at NPC-1.5 M.
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Nanoporous Carbon from Water Hyacinth Via Hydrothermal Carbonization
(2020-07-30)
Chanpee, Sirayu
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Suksai, Nattaya
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Kaewtrakulchai, Napat
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Chutipaijit, Sutee
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Fuji, Masayoshi
Nanoporous carbon materials have been successfully synthesized from water hyacinth via hydrothermal carbonization (HTC). This research was studied the effect of hydrothermal temperature from 160 - 200 C and reaction time for 4 - 24 h. Afterwards, carbonization was carried out at the temperature of 600 - 900 C for 2 h in N2 atmosphere for developing porosity and even removing contaminants of hydrothermal char to obtain the porous carbon. The physico-chemical properties of nanoporous carbon materials were comprehensively characterized through Scanning electron microscope (SEM), Fourier transforms infrared spectroscopy (FT-IR), CHN elemental analysis, X-ray diffraction (XRD) and BET analysis. The adsorption capacity and carbon content of nanoporous carbon materials from water hyacinth were increased with increased hydrothermal carbonization temperature and time. Performing HTC at 200 C for 12 h. Is the optimum condition to synthesis of precursor materials for good adsorbent.
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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
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Kaewtrakulchai, Napat
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Fuji, Masayoshi
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Eiad-ua, Apiluck
High 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 m2/g with the total pore volume of 0.495 cm3/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.
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Valorization of horse manure conversion to magnetic carbon nanofiber for dye adsorption by hydrothermal treatment coupled with carbonization
(2024-06-01)
Kaewtrakulchai, Napat
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Chanpee, Sirayu
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Pasee, Warit
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Putta, Ampol
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Chutipaijit, Sutee
Pollution of water resources has recently increased as a result of expanded industrial activity. Recycling waste biomass into bio-adsorbent material offers a cheap, easy, and eco-friendly solution. In this study, magnetic carbon nanofibers (MCNF) with a highly porous structure were developed from magnetite-preloaded horse manure by hydrothermal treatment followed by carbonization using different ratios of iron (III) nitrate and iron oxide as magnetic precursors. The produced MCNF had a very porous structure with specific surface area of 435.31 m2/g and high carbon content. The magnetic characteristics of MCNF promoted by the presence of iron oxide species. The saturated magnetization of MCNF obtained from a 5:5 ratio of the magnetic precursors (iron (III) nitrate: iron oxide) was 2.48 emu/g. Synthesized MCNF was applied as a bio-adsorbent for methylene blue (MB) removal from aqueous solution, with results showing excellent dye adsorption of 92–99 %. MB adsorption was facilitated by pore filling, electrostatic contact, hydrogen bonding, and ion complexation. Experimental results indicated that the Freundlich isotherm and pseudo-second-order kinetic models concurred with the observed MB adsorption data, suggesting that the adsorption mechanism involved multilayered micropore interactions between magnetite and MB chemisorption. The resulting magnetic adsorbent was successfully removed from the aqueous solution by physical separation. Findings indicated that horse manure-derived MCNF could be used as an efficient bio-adsorbent to remove organic contaminants in wastewater.
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Synthesis of nanoporous material from lignin via carbonization assisted acid activation
(2020-01-01)
Ngamthanacom, Nutchaporn
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Kaewtrakulchai, Napat
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Chaiwat, Weerawut
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Chuenchom, Laemthong
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Fuji, Masayoshi
Waste lignin (WL) from the pulp mill and paper was studied for its potential application to prepare the nanoporous carbon with high porosity via carbonization assisted acid activation. The effect of acid activation such as HNO3, HCl, H2SO4, and H3PO4 on lignin transformation to nanoporous carbon investigated. The physicochemical properties of nanoporous carbon were comprehensively characterized through N2 sorption, Scanning electron microscope (SEM), X-ray diffraction (XRD), and Fourier transform infrared (FTIR), respectively. N2 sorption revealed that the condition using 5% vol of phosphoric acid activation at carbonization temperature of 700°C for 2 h exhibited the highly porous structure of carbon nanoparticles with a total pore volume of 0.035 cm3 /g. With the properly selecting process variables of waste lignin development could be producing high porosity nanoporous carbon.
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Catalytic deoxygenation of palm oil over metal phosphides supported on palm fiber waste derived activated biochar for producing green diesel fuel
(2022-09-13)
Kaewtrakulchai, Napat
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Fuji, Masayoshi
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Eiad-Ua, Apiluck
Palm oil conversion into green diesel by catalytic deoxygenation (DO) is one of the distinctive research topics in biorefinery towards a bio-circular-green economic model to reduce the greenhouse gas emissions. In this study, palm fiber waste was explored as an alternative precursor for the preparation of activated biochar as a support material. A new series of nickel phosphide (Ni-P) and iron phosphide (Fe-P) catalysts supported on palm fiber activated biochar (PFAC) was synthesized by wetness impregnation, and extensive characterization was performed by several techniques to understand the characteristics of the supported metal phosphide catalysts prior to palm oil deoxygenation for producing of green diesel (C<inf>15</inf>-C<inf>18</inf> hydrocarbons). The PFAC support exhibited suitable physicochemical properties for catalyst preparation, such as high carbon content, and high porosity (S<inf>BET</inf> of 1039.64 m2 g−1 with V<inf>T</inf> of 0.572 cm3 g−1). The high porosity of the catalyst support (PFAC) significantly promotes the metal phosphide nanoparticle dispersion. The DO of palm oil was tested in a trickle bed down flow reactor under hydrogen atmosphere. The outstanding catalytic performance of supported Ni-P and Fe-P catalysts provided an impressive liquid hydrocarbon yield between 63.37 and 79.65% with the highest green diesel selectivity of 62.64%. Decarbonylation (DCO) and decarboxylation (DCO<inf>2</inf>) are the main pathways for the relative phosphide catalysts as presented by the high number of C<inf>n−1</inf> atoms (C<inf>15</inf> and C<inf>17</inf> hydrocarbons). In addition, metal phosphide/PFAC catalysts could achieve great potential application as a promising alternative catalyst for biofuel production via deoxygenation for large-scale operation owing to their excellent catalytic activity, simple preparation, and utilization of sustainable resources.
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Synthesis of porous carbon materials from water hyacinth via hydrothermal carbonization assisted chemical activation for carbon-based electrode applications
(2020-10-26)
Liamprawat, Tanatorn
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Verasarut, Panupong
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Kaewtrakulchai, Napat
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Panomsuwan, Gasidit
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Chutipaijit, Sutee
Recently, lignocellulosic materials have been widely utilized as feedstocks for several applications such as carbon, biofuels and biochemical productions because of their potentials (i.e. waste reduction, carbon sequestration, renewable). In this study, porous carbon was successfully synthesized from water hyacinth (WHs) via hydrothermal carbonization assisted with chemical activation using Na2CO3 and K2CO3. The hydrothermal carbonization process was studied in the range of 160-200°C for 4-12h and the hydrothermal chars were then further pyrolyzed under a supply of N2 flow 100ml/min at 700-900°C for 2h. The as-pyrolyzed chars were then activated by two different bases including Na2CO3 and K2CO3 at the ratio of 1.0 (w/w, hydrothermal char: chemical) to obtain highly porous carbon. The results indicated that carbon percentage, surface area and porous structure were improved with the higher hydrothermal temperature showing the best results at 180°C for 8h. Moreover, the development of pore structure of WHs porous carbon was successfully by chemical activation with K2CO3.
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Potential of advanced microporous zeolites and mesoporous materials derived from natural precursors as supports for iron phosphide catalysts in bio-jet fuel production from palm oil (Elaeis guineensis)
(2025-06-10)
Tanwongwan, Worapak
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Sartsamai, Ruttasart
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Kaewmeesri, Rungnapa
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Faungnawakij, Kajornsak
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Chollacoop, Nuwong
Iron phosphide (FeP) has emerged as an efficient catalyst for converting palm oil, a biomass-derived feedstock, into bio-jet fuel through the hydrocracking process. The catalytic performance of FeP is strongly influenced by the choice of support material. In this study, microporous MWW-type zeolites (MCM-22 and MCM-36) and mesoporous materials (MCM-41 and MCM-48) were successfully synthesized from entirely natural precursors, silica derived from rice husk and aluminosilicate gel extracted from kaolin clay, via a hydrothermal method, and employed as supports for FeP catalysts. Among these materials, MCM-22 zeolite exhibited the highest microporosity, followed by zeolite MCM-36, resulting in superior acidity compared to the mesoporous materials, MCM-41 and MCM-48. FeP supported on MCM-22 (FeP/MCM-22) demonstrated the best catalytic performance, liquid hydrocarbon yield (∼33%), and bio-jet selectivity (∼78%) were obtained, outperforming FeP/MCM-36, FeP/MCM-41, and FeP/MCM-48. This is due to its high surface area of micropores (∼187 m2 g−1) and the excellent acidity of this zeolite, which helped prevent FeP overloading and promote uniform metal distribution. Furthermore, it exhibited remarkable stability and reusability, with performance improving over three consecutive reaction cycles, LHCs yield increasing to 50% and bio-jet selectivity stabilizing at about 83%, attributed to enhanced acidity accessibility and progressive formation of the FeP active phase.
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Highly porous carbon materials for adsorbent from water hyacinth via hydrothermal carbonization
(2020-10-26)
Chanpee, Sirayu
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Suksai, Nattaya
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Kaewtrakulchai, Napat
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Chutipaijit, Sutee
;
Fuji, Masayoshi
Carbon nanoparticles have been successfully synthesized from waste lignin via carbonization and base activation. The effect of base activation on lignin transformation to carbon nanoparticles was investigated. Carbon nanoparticles from waste lignin via carbonization and base activation were denoted as CNPs. The physicochemical properties of CNPs were comprehensively characterized through a Scanning electron microscope (SEM), X-ray diffraction (XRD), and Raman spectroscopy. The results revealed that the condition using 5 wt% of sodium hydroxide (NaOH) and carbonization at 700°C on N2 atmosphere exhibited the highly porous structure of carbon nanoparticles. In conclusion, the NaOH-treated CNPs led to the production of high specific surface areas and high micropore volumes.
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Cattail (Typha angustifolia) flower-derived porous carbons as support of electroplated Ni and Cu catalysts for hydrogenation of methyl levulinate to γ-valerolactone
(2023-09-01)
Kaewtrakulchai, Napat
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Gunpum, Wachiraporn
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Fuji, Masayoshi
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Eiad-Ua, Apiluck
The novel synthesis of carbon-supported metal catalysts was completely developed by using electroplating technique. A carbon support was prepared from cattail (Typha angustifolia) flowers (CF) as a bio-material precursor through a hydrothermal process combined carbonization. The prepared carbons exhibited a high surface area, porosity, and excellent electrical conductivity, which is relevant characteristics to materials utilized for metal catalyst supporter. In this study, electroplating technique has been applied for the catalyst synthesis to utilize in hydrogenation of methyl levulinate to γ-valerolactone. Interesting experimental parameters in electroplating such as metal precursors (Ni and Cu), solution temperatures (40, 45, 50, 55, and 60 °C), and applied voltages (3.0, 3.5. 4.0, 4.5, and 5.0 V) were thoroughly investigated on some characteristics of catalysts. The physicochemical properties of studied catalysts were comprehensively characterized by using high-resolution scanning electron microscopy (HRSEM) equipped with energy dispersive spectroscopy (EDS) and focused ion beam (FIB), X-ray diffraction (XRD), and nitrogen sorption analyzer to examine surface morphology, elemental compositions, distribution of the metal in cross-section surface, crystallinity, and textural pore characteristic, respectively. In electroplating process, the solution temperature of 50 °C with the applied voltage of 4 V become an optimal condition for the synthesis of catalyst with uniformed metallic phase and high metal dispersion on carbon support. Ni-carbon and Cu-carbon catalysts exhibited an excellent catalytic activity with the methyl levulinate conversion of 32.68% and 29.17%, respectively.

Eiad-Ua, Apiluck

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