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

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Influence of crystallization time for synthesis of zeolite a and zeolite x from natural kaolin
(2019-01-01)
Srilai, Suphada
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Tanwongwan, Worapak
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Onpecth, Kobchai
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Wongkitikun, Thanapat
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Panomsuwan, Gasidit
Zeolite A and zeolite X were successfully synthesized from natural kaolin from Lampang province using calcination and a two-step hydrothermal method. First, metakaolin was obtained by calcining the kaolin at 700 °C for 2 h. Hydrothermal experiments can be separated into two types, being high temperature and short time or lower temperature long time. For high temperature hydrothermal treatment, metakaolin was mixed with NaOH to form hydrous sodium aluminosilicate. This was dissolved in dilute HCl. After filtration, the pH was adjusted with deionized water to pH = 7. This formed an amorphous aluminosilicate gel. For low temperature and longtime hydrothermal treatment aluminosilicate gel was mixed with NaOH to form zeolite A and zeolite X. The optimum condition for the first step in the synthesis of zeolite A is high temperature and short time of hydrothermal treatment with NaOH 8 M at 200 °C for 3 hours. This is followed by low temperature and longtime of hydrothermal treatment with NaOH 1 M carried out at 90 °C for 72 hours. The optimum conditions for the first step of synthesis of zeolite X is the high temperature, short time hydrothermal treatment with NaOH 8 M at 200 °C for 3 hours and low temperature, longtime hydrothermal treatment with NaOH 1 M at 90 °C for 120 hours. The characterizations of zeolite A and zeolite X were carried out by x-ray diffraction (XRD), scanning electron microscopy (SEM), and infrared spectroscopy (FT-IR).
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Effect of alkaline activation on low grade natural kaolin for synthesis of zeolite A
(2016-01-01)
Asawaworarit, Panuruj
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Chollacoop, Nuwong
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Viriya-Empikul, Nawin
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Eiad-Ua, Apiluck
The conventional technique to synthesizes zeolite A from kaolin is calcination. However, this technique has one drawback since, the impurities in kaolin, such as muscovite and quartz, remain. Therefore, the hydrothermal process without calcination is used to synthesize high purity zeolite A. Hydrothermal synthesis without calcination can be separated into two steps, namely first and second hydrothermal steps. Alkaline activation reaction in the first hydrothermal step was used to study the effect of NaOH concentration ranging from 4M, 6M, 8M, 10M to 12M at 200°C for 3 hours. In this step, sodium aluminosilicate (cancrinite and nepheline hydrate) was produced and then dissolved in HCl. After filtration, the impurity was removed, and adjusted for neutral pH of 7 to form amorphous aluminosilicate gel. For the second hydrothermal step, amorphous gel was mixed with NaOH (1-4M) to form zeolite A at 90°C for 3 days. The x-ray diffraction (XRD) and Scanning Electron Microscope (SEM) were used for characterization.
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Synthesis of Zeolite Y from Kaolin via hydrothermal method
(2019-01-01)
Krongkrachang, Pimpetch
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Thungngern, Pimpreeya
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Asawaworarit, Panuruj
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Houngkamhang, Nongluck
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Eiad-Ua, Apiluck
ZeoliteY has been successfully synthesized via a two-step hydrothermal method with kaolin from Lampang province as a precursor. For the first hydrothermal, kaolin with an addition of sodium silicate (NaSi<inf>3</inf>O<inf>7</inf>) or tetraethyl orthosilicate (TEOS) was mixed with sodium hydroxide (NaOH) and autoclaved for 200oC at different reaction times for 6, 8 and 10 h, respectively. Sodium hydroxide and hydrochloric acid were added into the compound mixture to adjust its pH before it was formed into gel. After a second time hydrothermal at 90°C for 2 days, the solid product was filtered out, washed by deionized water and dried overnight. The zeolite was then characterized by X-ray diffraction spectroscopy (XRD) to identify type and crystallization, scanning electron microscopy (SEM) for morphology, Fourier transform infrared spectroscopy (FTIR) to identify its functional group and N<inf>2</inf> adsorption to study the adsorption/desorption isotherm and pore distribution. From N<inf>2</inf> adsorption-desorption isotherm, it is revealed that the zeolite obtained by this method have 571 m2/g surface area and pore size distribution around 4.89 nm.
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Fantastic carbon material for nickel/carbon support catalyst reducing via calcination enhanced with hydrothermal carbonization
(2016-01-01)
Jomhataikool, Buntita
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Gunpum, Wachiraporn
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Kraithong, Wasawat
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Viriya-Empikul, Nawin
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Eiad-Ua, Apiluck
In generally, the metal catalyst which synthesis by conventional techniques is usually in metal oxide form or easily oxidize in the air thus the metal catalyst must reduce to metallic form before using. It was complex process and dangerous. In the research, Carbon material from cattail flower (CF) were used as supporter of Nickel/Carbon supported metal catalyst (Ni/C). This research were studied effect of used carbon material from CF as supporter of Ni/C and varying nickel loading. The Ni/C catalyst were prepared by hydrothermal, impregnation and calcination process. Firstly, Dried CF has been pretreat via hydrothermal process with optimized condition at 180°C for 8h. Then, the nickel solution was added to support via impregnation method by varying Ni loading from 20 to 60 wt% of supported. Finally, the sample has been pelleted into 0.5mm-Ni/C pellet and calcined at 900°C for 2h under nitrogen atmosphere. Ni/C were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), Energy dispersive X-ray (EDX), surface area and pore size distribution was determined by N2 adsorption. The result indicate that nickel particle on Ni/C were in the free metal from without reduction and well dispersed on supported surface. Particle size and surface area of Ni/C were decreases at the increase metal loading. Nickel/Carbon supported metal catalyst were ready to use and could be controlled particle size, surface area and crystallinity by metal loading.
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Influence of hydrothermal-carbonization process on biochar properties from cattail weed waste
(2019-01-01)
Smuthkochorn, Araya
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Katunyoo, Nardnutda
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Kaewtrakulchai, Napat
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Atong, Duangduen
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Soongprasit, Kanit
Biochars have been successfully synthesized from Cattail leave (CL) via hydrothermal and carbonization process. The experimental work described has focused on physical properties of biochars produced from Cattail leaves at 160, 180 and 200°C for 8, 12 and 24 h for hydrothermal and substituted to carbonization at 700°C for 2 h. The influences of hydrothermal and carbonization on the pore structure, surface functional groups and the product yield was also investigated by characterization using Scanning Electron Microscope (SEM) and Fourier Transform Infrared Spectroscopy, respectively. Although the morphologies of cell structures were maintained in the hydrothermal and carbonization, it was found that the yield of produced biochar was decreased with increase of the hydrothermal temperature and time. The images from SEM showed that the pore structures are quite roughness on their external surface of biochar and the functional group of their surface area has most of pure carbon content (59-65 wt%).
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Zeolite P from kaolin via hydrothermal method
(2018-09-05)
Eiad-Ua, Apiluck
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Amnaphiang, Phanwasa
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Asawaworarit, Panuruj
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Houngkamhang, Nongluck
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Chollacoop, Nuwong
Zeolite P has been successfully synthesized from natural kaolin via two step hydrothermal process. The natural kaolin from Lampang, Thailand was studied for this research. In first hydrothermal, kaolin was mixed with sodium hydroxide solution at 200 oC for different reaction times from 3 - 5 hours, respectively.Sodium hydroxide and hydrochloric acid were added into the mixture to adjust their pH before they were formed into gel. Second hydrothermal process, the gel was kept of 90 oC for 3 days to obtain zeolite P. Synthesized zeolite P was characterized by X-ray diffraction (XRD) for identification the type and crystallization. Besides, the morphology was characterized by scanning electron microscopy)SEM.(The functional group was characterized by Fourier-transform infrared spectroscopy (FTIR). From this study, it was found that the increasing of reaction time in first hydrothermal activation and hydrochloric acid concentration lead to the high quality of zeolite P.
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Characterization of carbon fibers from Thai horse manure via hydrothermal carbonization
(2018-01-01)
Wettayavong, Sorakit
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Sangnoi, Siwakron
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Kaewtrakulchai, Napat
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Eiad-Ua, Apiluck
Carbon fibers from biomass have been successfully prepared via hydrothermal-carbonization and activated in air atmosphere for catalyst supporter. In this research, we study the effect of temperature (160-200 °C) and residence time (4-24 h) to pretreat the initial carbon precursor in terms of chemical properties (i.e. carbon content, surface functional group) including the physical properties such as porosity and total surface areas. Afterwards, carbonization was obtained at the temperature of 300 °C for 2h for developing the porosity and even removing the contaminants of hydrothermal char to reach the carbon fiber. Nevertheless, carbon fiber was characterized. Scanning electron microscopy (SEM) and Functional Transform Infrared spectroscopy (FTIR) were employed to characterize physical morphology and functional group on the surface, respectively.
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Preparation of nanocomposite particles from Typha Angustifolia and Egg Shells
(2014-01-01)
Eiad-Ua, Apiluck
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Insuang, Koonyada
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Changsuwan, Supattra
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Viriya-Empikul, Nawin
Nanocomposite Paticles have been successfully synthesized from Typha Angustifolia and Egg Shells via 3 steps synthesis; hydrothermal, pyrolysis and/or ball milling techniques, respectively. Typha Angustifolia was subjected to produce fine carbon particles by two stage processes of hydrothermal (at 200°C for 4 h) and carbonization technique (under Argon atmosphere at 700°C for 2 h) while the egg shells were convert to white powder (calcium oxide) by calcining under air atmosphere at 900°C for 4 h. The samples have been characterized by scanning electron microscopy (SEM) and fourier transform infrared spectroscopy (FTIR) to investigate the morphology and surface function, respectively. The experimental results revealed that the planetary mill have effect on the composites between carbon and calcium. Calcium was deposited on the surface of carbon material. Moreover, when the calcium was increased leading to higher performance of milling (i.e. the smaller composite product was observed). © (2014) Trans Tech Publications, Switzerland.
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Combination of natural silica and alumina sources for synthesis of MCM-22 zeolite
(2023-08-01)
Tanwongwan, Worapak
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Chollacoop, Nuwong
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Faungnawakij, Kajornsak
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Assabumrungrat, Suttichai
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Nakhanivej, Puritut
Zeolite has become a promising material that can potentially play a pivotal role in resolving environmental crises. Among zeolite families, MCM-22 zeolite shows outstanding intrinsic properties associated with the topology and porous structure, offering ion-exchange advantages for catalytic activity processes. The synthesis of MCM-22 zeolite becomes challenging when concerning the cost and catalytic performance. To overcome this bottleneck, we demonstrate a sustainable route of a hydrothermal process using natural resources as starting materials. Rice husk from agricultural waste was used as a silica source while natural clays (kaolin and bentonite) were applied as alumina sources. The products from natural sources were compared with the use of commercial starting materials, e.g., NaAlO<inf>2</inf> (for alumina) and Na<inf>2</inf>SiO<inf>3</inf> and TEOS (for silica), in points of crystal, compositional, and morphological views. We showed that the high purity of MCM-22 zeolite can be obtained from rice husk silica (RHS) and aluminosilicate gel (ASG) extracted from kaolin, while the use of ASG extracted from bentonite tended to be unsuitable to generate the zeolite formation. We also studied the effects of reaction time and the ratio of RHS/ASG on the crystallinity and surface area of MCM-22. The architecture and acidity of an optimal product were explored by Nuclear magnetic resonance spectroscopy and Temperature-programmed desorption of ammonia, demonstrating the success of achieving well acidity.
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Influence of temperature and alkaline activation for synthesis zeolite a from natural kaolin
(2017-01-01)
Thungngern, Pimpreeya
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Amnaphiang, Phanwatsa
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Asawaworarit, Panuruj
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Goodwin, Vituruch
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Chollacoop, Nuwong
Zeolite A from natural kaolin have been successfully synthesized via calcination and hydrothermal. However, these techniques have one drawback since, the impurities in kaolin such as muscovite and quartz in the kaolin structure, which depend on temperature and alkaline activation. This work was separated into two steps, first step was used calcination technique, and second step was used hydrothermal technique. Reaction of temperature in the first step was studied the influence of temperature from 500°C to 800°C for 3 hours. In this step, kaolin transformed to metakaolin and remain the impurities. Next, reaction of alkaline activation in second step was studied about the influence of NaOH. The concentration of NaOH in hydrothermal was varied from 1M to 4M and mixed with metakaolin at 90°C for 72 hours. X-ray Diffraction Spectroscopy (XRD), Scanning Electron Microscopy (SEM) and Fourier Transform Infrared Spectroscopy (FTIR) were used for characterization. The solid products were formed to zeolite A at 1M NaOH hydrothermal with 500oC to 800oC calcination and it can be seemed good of euhedral structure at 700oC.

Eiad-Ua, Apiluck

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