• Clean Technology
• /
• v.24 no.3
• /
• pp.206-211
• /
• 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.

• Journal of Korean Society for Atmospheric Environment
• /
• v.17 no.E3
• /
• pp.117-124
• /
• 2001

The present paper examined the kinetics of photocatalytic degradation of volatile organic compounds (VOCs) including gaseous trichloroethylene (TCE) and acetone. In this study, we examined the effects of the initial concentration of VOCs and the light intensity of ultra-violet (UV). A batch photo-reactor was specifically designed for this work. The photocatalytic degradation rate increased with the initial concentration of VOCs but remained almost constant beyond a certain concentration. It matched well with the Langmuir-Hinshelwood (L-H) kinetic model. When the effect of light intensity was concerned, it was found that photocatalytic degradation occurs in two regimes with respect to light intensity.

• Bulletin of the Korean Chemical Society
• /
• v.33 no.11
• /
• pp.3691-3695
• /
• 2012

Photocatalytic reduction of hexavalent chromium (Cr(VI)) in ferric-tartrate system under irradiation of visible light was investigated. Effects of light resources, initial pH value and initial concentration of various reactants on Cr(VI) photocatalytic reduction were studied. Photoreaction kinetics was discussed and a possible photochemical pathway was proposed. The results indicate that Fe(III)-tartrate system is able to rapidly and effectively photocatalytically reduce Cr(VI) utilizing visible light. Initial pH variations resulte in the concentration changes of Fe(III)-tartrate complex in this system, and pH at 3.0 is optimal for Cr(VI) photocatalytic reduction. Efficiency of Cr(VI) photocatalytic reduction increases with increasing initial concentrations of Cr(VI), Fe(III) and tartrate. Kinetics analysis indicates that initial Fe(III) concentration affects Cr(VI) photoreduction most significantly.

• Journal of Environmental Science International
• /
• v.12 no.10
• /
• pp.1071-1077
• /
• 2003

The aim of this study is, firstly, to find out what kinds of inorganic species are produced in the photocatalytic oxidation of ammonium-nitrogen containing water and, secondly, to seek the influence of anion for the photocatalytic oxidation of ammonium contained compounds. The photoenergy above 3 eV(λ <415 nm) was effectively absorbed by TiO$_2$ and TiO$_2$/polymer was used to be oxidized NH$_4$-N in wastewater to NO$_3$-N. Existing the anion as Cl$\^$-/, the rate of photocatalytic oxidation decreased regardless of other condition. This result showed that the chloride ions reduced the rate of oxidation by scavenging oxidizing radical species as OH$\^$-/ and OCl$\^$-/. Some of the added ion might have blocked the active sites of the catalyst surface, thus deactivated the catalyst.

• Proceedings of the Korean Vacuum Society Conference
• /
• 2010.02a
• /
• pp.34-34
• /
• 2010

Activities of various $TiO_2$ nanostructures in photocatalytic decomposition of methylene blue and toluene were determined in order to shed light on the relationship between structures and photocatalytic activity. Commercially available P-25 samples were used in the present work. In addition, $TiO_2$ nanostructures were synthesized using atomic layer deposition (ALD). We show that change in the surface structure of $TiO_2$ upon variois surface treatments results in variation in photocatalytic activity. In particular, increase in the number of OH groups on the surface leads to the enhancement in photocatalytc activity. Surface OH groups increases adsorption reactivity of organic reactants, thereby increasing activity in photocatalytic decomposition of methylene blue and toluene.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
• /
• v.32 no.2
• /
• pp.161-164
• /
• 2019

This study describes the development of graphene-$TiO_2$ conjugates for the enhancement of the photocatalytic efficiency of $TiO_2$. Graphene-based hybrid nanomaterials have attracted considerable attention because of the unique and advantageous properties of graphene. In the proposed hybrid nanomaterial, graphene serves as an electron acceptor to ensure fast charge transfer. Effective charge separation can, therefore, be achieved to slow down electron-hole recombination. This results in an enhancement of the photocatalytic activity of $TiO_2$. In addition, increased adsorption and interactions with the adsorbed reagents also lead to an improvement in the photocatalytic activity of graphene-$TiO_2$ hybrid nanomaterials. The acquired result is encouraging in that the photocatalytic activity of $TiO_2$ was initiated using visible light (630 nm) instead of the typical UV light.

• Proceedings of the Korean Institute of Building Construction Conference
• /
• 2023.05a
• /
• pp.181-182
• /
• 2023

The purpose of this study is to enhance the photocatalytic properties of a mixture of low-cost titanium dioxide and calcium carbonate through a simple mixing process. To increase the photocatalytic activity, the weight ratio of titanium dioxide to calcium carbonate was selected as a variable. Photocatalytic activity was evaluated by measuring the degradation of methylene blue and NOx under ultraviolet light. The results showed that a mixture containing 60% titanium dioxide and 40% calcium carbonate exhibited the highest photocatalytic activity.

• Korean Chemical Engineering Research
• /
• v.61 no.4
• /
• pp.635-644
• /
• 2023

Due to the rapid development of the livestock industry, particularly due to residual pharmaceutical antibiotics, environmental populations have been negatively affected. Herein, we report a ZnO/melamine-functionalized carboxylic-rich graphene oxide (ZFG) photocatalyst for visible light-driven photocatalytic degradation of tetracycline hydrochloride in aqueous solutions. The properties of the photocatalysts were evaluated by XRD, FTIR, XPS, Fe-SEM, HR-TEM, TGA, Raman spectroscopy, UV-Vis spectroscopy, zeta potential, and electrochemical measurements. The photocatalytic activity was measured using high-performance liquid chromatography. The photocatalytic properties of the ZFG photocatalyst evaluated against the tetracycline hydrochloride (TCH) antibiotic under visible light irradiation showed superior photodegradation of 96.27% within 60 min at an initial pH of 11. The enhancement of photocatalytic degradation was due to the introduction of functionalized graphene, which increases the light-harvesting capability and molecular adsorption capability in addition to minimizing the recombination rate of photogenerated charge carriers due to its role as an electron acceptor and mediator.

• Journal of Environmental Science International
• /
• v.12 no.12
• /
• pp.1255-1260
• /
• 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.

• Membrane Journal
• /
• v.17 no.3
• /
• pp.244-253
• /
• 2007

This research investigated the effect of a photocatalytic reaction on nanofiltration(NF) membrane fouling by natural organic matter(NOM). The photocatalytic degradation was very effective for destruction and transformation of NOM and was carried out by titanium dioxide($TiO_2$) and $TiO_2$-immobilized bead as a photocatalyst. In order to compare their phtocatalytic properties, the photocatalytic degradation of humic acid in the presence of calcium ion was used as a model reaction. After the photocatalytic degradation the membrane fouling was dramatically decreased.