• Environmental Engineering Research
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• 제25권4호
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• pp.597-604
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• 2020

In the present study, the application of sequential biological and photocatalytic process was evaluated as a feasible process for the degradation of imidacloprid (IMI) in soil. Photocatalysis was carried out as a post and pre-treatment to the biological process as Microbial Photocatalytic (MP) and Photocatalytic Microbial (PM), respectively, to enhance the degradation and mineralization of IMI in soil. By both the processes, there was an enhancement in the percentage degradation of IMI i.e 86.2% for PM and 94.6% for MP process. The obtained results indicate that MP process is apparently more efficient in degradation of IMI which was observed with 15 days of biological treatment followed by 18 h of photocatalytic degradation (15 d + 18 h). The present work also reveals that though the difference in terms of the degradation of IMI after 5 d + 18 h, 10 d + 18 h & 15 d+ 18 h of MP process is not drastic, yet significant variation has been observed in terms of mineralization that truly signifies the removal of IMI from the soil. The LC analysis has shown that the intermediates formed during MP process are more and smaller in comparison to PM process, which further provides evidence that MP process is better than PM process for effective degradation of IMI in soil.

• 한국환경과학회지
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• 제12권12호
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• pp.1255-1260
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• 2003

Plasma-photocatalytic oxidation process was applied in the decomposition of Triethylamine(TEA) and Methyl ethyl ketone(MEK). Plasma reactor was made entirely of pyrex glass and consists of 24mm inner diameter, 1,800mm length and discharge electrode of 0.4mm stainless steel. And initial concentrations of TEA and MEK for plasma-photocatalytic oxidation are 100 ppm. Odor gas samples were taken by gas-tight syringe from a glass sampling bulb which was located at reactor inlet and outlet, and TEA and MEK were determined by GC-FID. For plasma process, the decomposition efficiency of TEA and MEK were evaluated by varying different flowrates and decomposition efficiency of TEA and MEK increased considerably with decreasing treatment flowrates. For photocatalytic oxidation process, also the decomposition efficiency of TEA and MEK increased considerably with decreasing treatment flowrates. The decomposition efficiency of MEK was 57.8％, 34.2％, 18.8％ respectively and the decomposition efficiency of TEA was reached all 100％. This result is higher than that of plasma process only, From this study, the results indicate that plasma-photocatalytic oxidation process is ideal for treatment of TEA and MEK.

• 청정기술
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• 제24권3호
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• pp.206-211
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• 2018

Lead molybdate ($PbMoO_4$) were successfully synthesized using a facile surfactant-assisted hydrothermal process and characterized by XRD, Raman, PL, BET and DRS. We also investigated the photocatalytic activity of these materials for the decomposition of Rhodamine B under UV-light irradiation. From XRD and Raman results, well-crystallized $PbMoO_4$ crystals have been successfully synthesized with a facile surfactant-assisted hydrothermal process and had 52-69 nm particle size. The $PbMoO_4$ catalysts prepared at $160^{\circ}C$ showed the highest photocatalytic activity. The PL peak was appeared at about 540 nm at all catalysts and it was also shown that the excitonic PL signal was proportional to the photocatalytic activity for the decomposition of Rhodamine B.

• 한국분말재료학회지
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• 제10권2호
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• pp.123-128
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• 2003

$TiO_2$ nanopowder was synthesized by chemical vapor condensation (CVC) process and its photocatalytic property depending on microstructure was considered in terns of decomposition rate of organic compound. In order to control microstructure of $TiO_2$ nanopowder such as particle size and degree of agglomeration, precursor flow rate representing number concentration was changed as a process variable. In TEM observation, spherical $TiO_2$ nanoparticles with average size of 20 nm showed gradual increases in particle size and degree of agglomeration with increase of precursor flow rate. Also decomposition rate of organic compound increased with decreasing precursor flow rate. Thus, it was concluded that photocatalytic property was enhanced by targe surface area of disperse $TiO_2$ nanoparticles synthesized at lower precursor flow rate condition in CVC process.

• 멤브레인
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• 제17권3호
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• pp.244-253
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• 2007

광촉매 반응이 자연유기물에 의한 나노여과막의 오염에 미치는 영향을 살펴보았다. 광촉매 분해공정은 자연유기물의 분해와 변형에 효율적이었으며 이산화티타늄과 고정화 비드를 광촉매로 사용하였다. 광촉매적 특성을 비교하기 위하여 칼슘 이온 존재 시의 휴민산의 광분해를 모델 반응으로 설정하였다. 광분해 전에는 치밀한 막오염층이 형성되어 막오염을 가속화시킨 반면, 광분해 후에는 막오염이 크게 감소하였다.

• 한국응용과학기술학회지
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• 제24권1호
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• pp.1-9
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• 2007

It prepared the $TiO_2$ powder which has photo-catalytic activity in the visible-light by the wet process with titanium oxysulfate. The titanium $dioxide(TiO_2)$ by the wet process creates a new absorption band in the visible light region, and is expected to create photocatalytic activity in this region. Anatase $TiO_2$ powder which has photocatalytic activity in the visible light region, is treated using microwave and radio-frequency(RF) plasma. But, the $TiO_2$ powder for the visible light region, which also can be easily produced by wet process. The wet process $TiO_2$ absorbed visible light between 400nm and 600nm, and showed a high activity in this region, as measured by the oxidation removal of aceton from the gas phase. The AH-380 sample appears the yellow color to be strong, the catalytic activity in the visible ray was excellent in comparison with the plasma-treated $TiO_2$. The AH-380 $TiO_2$ powder, which can be easily produced on a large scale, is expected to have higher efficiency in utilizing solar energy than the plasma-treated $TiO_2$ powder.

• 한국재료학회지
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• 제26권2호
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• pp.73-78
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• 2016

$TiO_2$ nanoparticles were synthesized by a sol-gel process using titanium tetra isopropoxide as a precursor at room temperature. Ag-doped $TiO_2$ nanoparticles were prepared by photoreduction of $AgNO_3$ on $TiO_2$ under UV light irradiation and calcinated at $400^{\circ}C$. Ag-doped $TiO_2$ nanoparticles were characterized for their structural and morphological properties by X-ray diffractometry (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and transmission electron microscopy (TEM). The photocatalytic properties of the $TiO_2$ and Ag-doped $TiO_2$ nanoparticles were evaluated according to the degree of photocatalytic degradation of gaseous benzene under UV and visible light irradiation. To estimate the rate of photolysis under UV (${\lambda}=365nm$) and visible (${\lambda}{\geq}410nm$) light, the residual concentration of benzene was monitored by gas chromatography (GC). Both undoped/doped nanoparticles showed about 80 % of photolysis of benzene under UV light. However, under visible light irradiation Ag-doped $TiO_2$ nanoparticles exhibited a photocatalytic reaction toward the photodegradation of benzene more efficient than that of bare $TiO_2$. The enhanced photocatalytic reaction of Ag-doped $TiO_2$ nanoparticles is attributed to the decrease in the activation energy and to the existence of Ag in the $TiO_2$ host lattice, which increases the absorption capacity in the visible region by acting as an electron trapper and promotes charge separation of the photoinduced electrons ($e^-$) and holes ($h^+$). The use of Ag-doped $TiO_2$ nanoparticles preserved the option of an environmentally benign photocatalytic reaction using visible light; These particles can be applicable to environmental cleaning applications.

• 청정기술
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• 제21권3호
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• pp.178-183
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• 2015

PbMoO₄ 산화물을 수열합성법과 마이크로파 공정으로 합성하여 XRD, DRS, BET, Raman, SEM 및 PL 등에 의해 특성분석을 하였고, 자외선 조사 하에서 Rhodamine B의 광분해 반응에서의 활성을 조사하였다. XRD 및 Raman의 분석 결과로부터 대부분의 촉매들은 제조방법과 무관하게 잘 결정화된 PbMoO₄ 구조를 가지고 있었으며 42에서 59 nm의 크기를 나타내었다. 마이크로파 공정으로 제조된 PbMoO₄ 촉매는 통상적인 수열합성법으로 제조된 촉매에 비해 균일한 입자를 가지고 있으며, 높은 광분해 활성을 나타내었다. 마이크로파 주사 시간을 75분으로 제조한 PbMoO₄ 촉매가 가장 높은 광분해 활성을 나타내었다. 모든 촉매들은 530 nm 부근에서 강하고 넓은 PL 흡수밴드가 나타났으며, 이 피크의 세기가 커질수록 광분해 활성이 증가하는 것으로 나타났다.

• 청정기술
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• 제27권4호
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• pp.291-296
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• 2021

물에 잔존하는 유기오염물질이 인체 및 환경에 미치는 악영향을 해결하기 위한 방법으로 오염물질을 친환경적으로 분해할 수 있는 광촉매 기술이 대두되고 있다. 대표적인 광촉매 물질로 TiO₂ 입자가 사용되고 있지만 비싼 가격으로 인해 이를 대체하고자 하는 노력이 지속적으로 수행되었다. 본 연구에서는 이러한 노력의 일환으로 미세유체공정을 사용하여 보다 가격경쟁력이 우수한 ZnO입자를 합성하였다. ZnO의 넓은 밴드갭으로 인해 촉매활성이 제한되는 단점을 해결하고자 동일 공정을 사용하여 은(Ag) 나노입자를 ZnO 표면에 증착하여 Ag-ZnO 나노복합체를 생산하였다. 다양한 분석법을 사용하여 나노복합체의 형상, 구조, 및 성분 분석을 진행한 결과 고품질의 Ag-ZnO 나노복합체가 합성됨을 확인했으며, 메틸렌블루 분해 실험을 통해서 광촉매 활성을 측정하였다. Ag-ZnO 나노복합체의 플라스몬 효과와 광반응에 의해 생성된 전자와 정공의 분리 효과에 의해 광촉매 활성 효율이 순수한 ZnO 입자와 비교하여 향상되었음을 확인하였다. Microreactor-assisted nanomaterials (MAN) 공정 기반의 나노복합체는 가격경쟁력이 우수하고 공정이 용이하다는 장점이 있기에 나노복합체 광촉매를 대량 생산하기 위한 잠재력이 우수하다고 사료된다.

• Korean Chemical Engineering Research
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• 제57권2호
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• pp.185-197
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• 2019

Deactivation of porous photocatalytic materials was studied using three types of microstructured particles: macroporous titania particles, titania microspheres, and porous silica microspheres containing CNTs and $TiO_2$ nanoparticles. All particles were synthesized by emulsion-assisted self-assembly using micron-sized droplets as micro-reactors. During repeated cycles of the photocatalytic decomposition reaction, the non-dimensionalized initial rate constants (a) were estimated as a function of UV irradiation time (t) from experimental kinetics data, and the results were plotted for a regression according to the exponentially decaying equation, $a=a_0\;{\exp}(-k_dt)$. The retardation constant ($k_d$) was then compared for macroporous titania microparticles with different pore diameters to examine the effect of pore size on photocatalytic deactivation. Nonporous or larger macropores resulted in smaller values of the deactivation constant, indicating that the adsorption of organic materials during the photocatalytic decomposition reaction hinders the generation of active radicals from the titania surface. A similar approach was adopted to evaluate the activation constant of porous silica particles containing CNT and $TiO_2$ nanoparticles to compare the deactivation during recycling of the photocatalyst. As the amount of CNTs increased, the deactivation constant decreased, indicating that the conductive CNTs enhanced the generation of active radicals in the aqueous medium during photocatalytic oxidation.