Publications by authors named "Thanapha Numpilai"

This study explores the modification of pore structures in porous silica materials synthesized using sodium silicate and waste gelatin, under varying silica-to-gelatin ratios. At ratios of 1.0-1.

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This study investigates the impact of microporous (SP-C) and micro-mesoporous carbon (DP-C) supports on the dispersion and phase transformation of iron oxides and their arsenic (V) removal efficiency. The research demonstrates that carbon-supported iron oxide sorbents exhibit superior As(V) uptake capacity compared to unsupported FeO, attributed to reduced iron oxide crystallite sizes and As(V) adsorption on carbon supports. Maximum As(V) uptake capacities of 23.

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Purification of As(V)-contaminated water through adsorption by FeO-based materials is a promising technology due to its low-cost and high efficiency. Dispersing the FeO phase on silica supports can improve both the adsorption rate and capacity due to the reduction in FeO particle sizes and the prevention of clumping of the FeO particles. However, the clusters in conventional silica materials largely impede the diffusion of As(V) to reach the FeO sites dispersed inside the clusters.

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Low cost FeO-based sorbents with an exceptional selectivity toward the targeted As(V) pollutant have gained extensive attention in water treatment. However, their structural features often influence removal performance. In this respect, we present herein a rational design of silica-supported FeO sorbents with an enhanced morphological structure based on a simple temperature-induced process.

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Arsenic (As) contamination in aqueous media is a major concern due to its adverse impacts on humans and the ecosystem more broadly because of its non-biodegradability. Consequently, an effective and selective sorbent is needed urgently to scavenge As pollutant. Herein, the adsorption behaviors of As(V) by FeO and FeO supported on different silica materials, consisting of unimodal mesoporous silica (FeO/U-SiO) and dual meso-macroporous silica (FeO/B-SiO), were compared to examine their structure-efficiency relationships in the elimination of As(V).

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Recycling of waste glycerol derived from biodiesel production to high value-added chemicals is essential for sustainable development of Bio-Circular-Green Economy. This work studied the conversion of glycerol to 1,3-propanediol over Pt/WO/AlO catalysts, pointing out the impacts of catalyst pore sizes and operating conditions for maximizing the yield of 1,3-propanediol. The results suggested that both pore confinement effect and number of available reactive metals as well as operating conditions determined the glycerol conversion and 1,3-propanediol selectivity.

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Impact of pore characteristics of porous silica supports on loading capacity and release behavior of ibuprofen was investigated. The porous silica materials and ibuprofen-loaded porous silica materials were thoroughly characterized by N2-sorption, thermal gravimetric and derivative weight analyses (TG-DTW), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), transmission electron microscope (TEM) to determine the physical properties of materials, amount of ibuprofen adsorbed and position of ibuprofen. The detailed characterization reveals that the ibuprofen molecules adsorbed inside the mesopores.

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