• Journal of the Korean Recycled Construction Resources Institute
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• v.4 no.4
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• pp.388-395
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• 2016

This paper explores the photocatalytic sensitivity of cement mortar incorporated with recycled $TiO_2$ from waste water sludge. Basically, $TiO_2$ cluster sank down slowly to the bottom of cement mortar specimen before setting and hardening process. This leads the mismatch of $TiO_2$ concentration on the top and the bottom faces of a specimen. This poorly dispersed $TiO_2$-cement mortar naturally exhibits poor NOx removal efficiency especially on the top of cementitious structure. In architectural engineering application such as building or housing structures, one can simply filp over from the bottom so that more $TiO_2$ concentrated surface can be placed outward into the air. However, in highway pavement case, this could not be applicable due to in-situ installation of concrete pavement. Hence, the dispersion of $TiO_2$ cluster inside the cementitous material is getting important issue onto road construction application. To elaborate this issue, according to our results, silica fume, high-ranged water reducer, viscosity agent, blast furnace slag were not enhanced much of dispersion characteristics of $TiO_2$ cluster. The combination of foaming agent and accelerator of hardening with viscosity agent and small grain size of fine aggregate may help the dispersion of $TiO_2$ inside cementitious materials. Even though the enhanced dispersion were applied to the specimen, NOx removal efficiency doest not change much for the top surface of the specimen. This concurrently affected by the presence of tiny air voids and the dispersion of $TiO_2$ in that these voids could easily adsorbed NOx gas with the aid of large surface area.

• Journal of the Korean Institute of Gas
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• v.27 no.3
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• pp.19-26
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• 2023

Hydrogen, a clean energy source free of COx emissions, is poised to replace fossil fuels, with its usage on the rise. Despite its high energy content per unit mass, hydrogen faces limitations in storage and transportation due to its low storage density and challenges in long-term storage. In contrast, ammonia offers a high storage capacity per unit volume and is relatively easy to liquefy, making it an attractive option for storing and transporting large volumes of hydrogen. While NH₃ decomposition is an endothermic reaction, achieving excellent low-temperature catalytic activity is essential for process efficiency and cost-effectiveness. The study examined the effects of different zeolite types (5A, NaY, ZSM5) on NH₃ decomposition activity, considering differences in pore structure, cations, and Si/Al-ratio. Notably, the 5A zeolite facilitated the high dispersion of Ni across the surface, inside pores, and within the structure. Its low Si/Al ratio contributed to abundant acidity, enhancing ammonia adsorption. Additionally, the presence of Na and Ca cations in the support created medium basic sites that improved N₂ desorption rates. As a result, among the prepared catalysts, the 15 wt%Ni/5A catalyst exhibited the highest NH₃ conversion and a high H₂ formation rate of 23.5 mmol/g_cat·min (30,000 mL/g_cat·h, 600 ℃). This performance was attributed to the strong metal-support interaction and the enhancement of N₂ desorption rates through the presence of medium basic sites.

• Korean Chemical Engineering Research
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• v.51 no.1
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• pp.80-86
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• 2013

In this study, the photocatalytic reactor system equipped with photocatalyst-carrying-silica-media cartridges [photocatalytic reactor system (1)] was used to perform the treatment of waste air containing malodor and volatile organic compound (VOC). The result of its performance was evaluated and compared with that of the photocatalytic reactor system equipped with commercial photocatalyst-carrying-nonwoven filter-media cartridges [photocatalytic reactor system (2)]. In case of photocatalytic reactor system (1), at the 1st stage of run the removal efficiencies of ethanol and toluene continued to be 80% and 20%, respectively. However, unlike toluene, the removal efficiency of ethanol dropped to 40% at the end of the 1st stage of run. The removal efficiency of hydrogen sulfide decreased from 100% to 90%. At the 2nd stage of its run the removal efficiency of ethanol decreased to 10% while the removal efficiencies of hydrogen sulfide and toluene remained as same as 90% and 20%, respectively, even though the inlet load of toluene increased by factor of four. In the 3rd stage of its run, as the result of application of aluminium-coated reflector film to the inner wall of photocatalytic reactor system, the removal efficiencies of ethanol and toluene increased by 5% to be 15% and 25%, respectively. In case of photocatalytic reactor system (2), at the 1st stage of its run, the removal efficiencies of ethanol, hydrogen sulfide and toluene continued to be 10%, 97% and 100%, respectively. However, at 2nd stage of its run their removal efficiencies became 5%, 95% and 2~3%, respectively, which showed that the removal efficiencies of ethanol and hydrogen sulfide decreased insignificantly while the removal efficiency of toluene dropped significantly from the perfect elimination. Moreover, the reflector film did not affect the performance of photocatalytic reactor system (2) at all. Therefore the removal of ethanol, hydrogen sulfide and toluene by photocatalytic reactor system (2) was mainly attributed to hydrophobic adsorption of its nonwoven filter media and its extent of photocatalytic removal turned out to be negligible, compared to that of photocatalytic reactor system (1).