• Journal of Environmental Science International
• /
• v.12 no.7
• /
• pp.775-782
• /
• 2003

The photodegradations of pyrene, chrysene and benzo[a]pyrene that were similar in structure among polycyclic aromatic hydrocarbons (PAHs) were investigated with a low-pressure mercury lamp(the wavelength of 253.7 nm and UV output of 1.35${\times}$10$\^$-3/J/s). The optimum concentrations of TiO$_2$ and H$_2$O$_2$ on the photodegradation of pyrene, chrysene and benzo[a]pyrene were 1 g/L and 1.5${\times}$10$\^$-3/ M, respectively. By these optimum concentrations, their rates increased with increasing the concentration of TiO$_2$ and H$_2$O$_2$ because the amounts of OH radical formed increased, but for the higher concentrations than the optimum, their rates decreased with increasing those concentrations because the white turbidity phenomena occurs in case of TiO$_2$ and H$_2$O$_2$ acts as an OH radical inhibitor. The photodegradation rates among the photodegradation processes such as UV, UV/TiO$_2$, UV/H$_2$O$_2$, and UV/H$_2$O$_2$/TiO$_2$ decreased in the following sequences.: UV/H$_2$O$_2$/TiO$_2$> UV/H$_2$O$_2$> UV/TiO$_2$> UV.

• Applied Chemistry for Engineering
• /
• v.20 no.5
• /
• pp.511-516
• /
• 2009

Photodegradation characteristics of polyolefin composites were studied. Thermogravimetric analysis results suggest that the polyolefin blends used in this study have different amounts of talc. The mechanical behaviors of polyolefin blends, which experienced UV-irradiation in accordance with SAE J1960, are investigated using tensile and Izod impact tests. These results show that as the UV-exposure time increases, a significant drop in the elongation at break and impact strength at a low temperature are observed. This may be explained by the decreases in elastic energy derived from the scission of polymer molecular chains and the low density of entanglement after UV- photodegradation. Scanning electron microscopy observations indicate that no crack and surface damage are observed, while the additional talc particles are exposed, on the UV-exposed surfaces. The exposure of talc particles may be responsible for the discoloration of UV-exposed polyolefin blend surface. Observation using Fourier transform infrared spectroscopy (FT-IR) confirms the presence of photodegradation on the surface of UV-exposed polyolefin blend.

• Journal of Environmental Health Sciences
• /
• v.26 no.2
• /
• pp.49-58
• /
• 2000

The present study was performed to investigate photodegradation rate constants and degradation products of phosphamidon and profenofos by the USEPA method. The two pesticides were very stable in 16 days exposure of sunlight from September 3 to 22, 1999 and humic acid had no sensitizing effect on the photolysis of each pesticide in sunlight. In the UV irradiation test, phosphamidon was rapidly degraded as increasing UV intensity. In case of UV irradiation with TiO2 and with TiO2 powder amount, degradation of profenofos showed no significant difference with UV irradiation. Photodegradation rate of profenofos was slower than that of phosphamidon. In order to identify photolysis products, the extracts of degradation products were analyzed by GC/MS. The mass spectra of photolysis products of phosphamidon were at m/z 153 and 149, those of the profenofos were at m/z 208 and 240, respectively. It was suggested that the photolysis products of phosphamidon were 0, 0-dimethyl phosphate(DMP) and N, N-diethylchloroacetamide, those of profenofos were 4-bromo-2-chlorophenol and 0-ethyl-S-propyl phosphate.

• Journal of Environmental Science International
• /
• v.9 no.2
• /
• pp.151-158
• /
• 2000

Considerable interest has been shown in recent years towards utilizing $TiO_2$ particles as a photocatalyst in the degradation of harmful organic contaminants. In this study, photocatalytic degradation of diazinon which is extensively used as a pesticide in the agriculture field, has been investigated with UV-illuminated $TiO_2$ weight, UV wavelength, pH of the solution. Photodegradation rate increased with decreasing initial concentration of diazinon and with increasing pH of the solution. Photodegradation rate increased with increasing $TiO_2$ weight, but was nearly the same at $TiO_2$ weight of 1g/$\ell$, 2 g/$\ell$, i.e., for initial diazinon concentratin of 5 mg/$\ell$. UV wavelength affecting on the degradation rate of diazinon decreased in the order of 254 nm>312 nm> 365 nm. For $TiO_2$ weight of 1 g/$\ell$and initial diazinon concentration of 5 mg/$\ell$, the photodegradation removal of diazinon was 100% after 130 min in the case of 254 nm, but 95% in the case of 312 nm, and 84% in the case of 365nm, after 180 min. The photodegradation of diazinon followed a first order or a pseudo - first order reaction rate. For initial diazinon concentration of 5 mg/$\ell$, the rate constants(k) in UV and $TiO_2$(1 g/$\ell$)/UV system were $0.006 min^{-1} and 0.0252 min^{-1} at 254 nm, 0.0055 min^{-1} and 0.0104 min^{-1} at 312 nm, and 0.004 min^{-1}$ at 365 nm respectively.

• Journal of Environmental Science International
• /
• v.15 no.11
• /
• pp.1061-1067
• /
• 2006

Photodegradation of endosulfan alpha, beta, and sulfate known as the most toxic substance among organochlorine pesticides by UV irradiation was studied at experimental conditions such as different pH aqueous solution and reaction time. The initial concentration of endosulfan alpha, beta, and sulfate in aqueous solution was 500 ppb, respectively. The experiment of photodegradation was conducted in a quartz reactor equipped with a low pressure mercury lamp (100 W, 240 nm). The samples were withdrawn from the photo reactor at intervals of 0, 10 min, 30 min, 1 hr, 2 hr, and 4 hr. Endosulfan sulfate was never hydrolyzed and photodegraded in wide range of pH. At pH 5 and reaction time (240 min), endosulfan alpha was photodegraded up to 67%. Both endosulfan alpha and beta were started to photodegrade at pH 6.5 with the lapse of time, resulting in approximately 99.9% and 87.2% of photodegradation efficiency, respectively. Furthermore, at pH 9, endosulfan alpha and beta was partially hydrolyzed and photodegraded to 99.5% at 120 min of reaction time. During the photolysis, any photo-products of endosulfan alpha, beta, and sulfate were not observed.

• Journal of the Korean Ceramic Society
• /
• v.45 no.1
• /
• pp.43-47
• /
• 2008

The photocatalyst of $TiO_2$ coated on a fly ash composites (TCF) was prepared from precipitant dropping method to remove the acetaldehyde by photocatalytic reaction. The TCF were characterized by crystal aize, crystal structure and specific surface area. The photodegradation of acetaldehyde has been investigated using a UV-illuminated fixed photocatalytic reactor with TCF catalyst and P-25 catalyst in gas phase. The effect of photodegradation reaction conditions, such as initial concentration of acetaldehyde, concentration of oxidant in mixed gas and the light intensity on the photodegradation of acetaldehyde were investigated. P-25 catalyst showed the highest photodegradation of acetaldehyde and anatase $TiO_2$ coated TCF showed higher decomposition rate than rutile coated TCF. The photodegradation rate of acetaldehyde increased with the decrease of flow rate, initial concentration of acetaldehyde ($C_i$) and water vapor, however, it was increased with the increas of UV light intensity. The optimum conditions were weight of TCF=10 g, flow rate=50 ml/min $C_i$=100 ppm, concentration of oxygen=20%, concentration of water vapor=100 ppm.

• Textile Coloration and Finishing
• /
• v.23 no.2
• /
• pp.100-106
• /
• 2011

UV-curable water-repellent finish was carried out to impart one-side repellency to the PET fabrics using a formulation of a UV-active fluorocarbon agent and a water soluble photoinitiator. The aqueous formulation was padded on the PET fabrics and it was subsequently UV-cured. The unirradiated side of the cured fabrics was made to wetteable to water by the prolonged UV/ozone irradiation. The influence of photoinitiator concentration, agent concentration and UV energy for photodegradation on the performance of the finished fabrics were investigated. The difference in the functional property of front and back sides was examined by measuring water repellency at each side of the treated fabrics, which resulted in four rating difference between two-side. The UV-cured and photodegraded PET surfaces were characterized by ATR, ESCA and FE-SEM.

• Journal of Environmental Science International
• /
• v.11 no.6
• /
• pp.589-596
• /
• 2002

Photocatalytic degradation of chlorpyrifos and diazinon, which are extensively used as an organophosphorous pesticide in the agriculture field, has been investigated with UV-radiated TiO$_2$ in aqueous phase. Photodegradation rate was increased with increasing pH of the solution. The removal efficiencies of chlorpyrifos and diazinon were 100% after 200 min in pH 9. Photodegradation followed a pseudo-first-order reaction. The rate constants of chlorpyrifos and diazinon were 0.0160min$\^$-1/ and 0.0180min$\^$-1/, respectively. NO$_3$$\^$-/, PO$_4$$\^$3-/, SO$_4$$\^$2-/ and Cl$\^$-/ were found as end products on the photocatalytic degradation of chlorpyrifos and diazinon with TiO$_2$/UV.

• Journal of the Korean Wood Science and Technology
• /
• v.23 no.3
• /
• pp.23-27
• /
• 1995

Several characteristic results of physical and optical properties of paper treated by UV light were obtained in the previous papers(Kim et al. 1988). In this paper, folding endurance and brightness of paper prepared by spraying photostabilizer were examined in order to elucidate photodegradation phenomena, UV light absorber and radical scavenger were most effective in preventing of folding endurance decrease. These results may be indicated that depolymerization of cellulose and hemicellulose chains leading to degradation of paper mechanical properties mainly caused by radical reaction. Ineffective hydroperoxide decomposer may be explained because of auto-oxidation reactions before forming stable compound from hydroperoxide.

• Journal of Environmental Science International
• /
• v.12 no.3
• /
• pp.337-344
• /
• 2003

The photodegradation of pyrene, chrysene and benzo［a］pyrene, that were similar in structure among poly-cyclic aromatic hydrocarbons (PAMs), were investigated in water irradiated with a low-pressure mercury lamp (wavelength of 253.7 nm and UV output of 1.35 ${\times}$ 10$\^$-3/J/s). The effects of several factors (t-BuOH, HCO$_3$$\^$-/ and pH) on photodegradation of above three PAHs were also examined. The photodegradation rates of PAHs decreased with increasing the concentration of t-BuOH, but decreased little with increasing the concentration of HCO$_3$$\^$-/ under the concentrations used in this study. The photodegradation rates of PAHs decreased with increasing pH, but their change were greater in case of pH increase from acid to neutral and were little in case of pH increase from neutral to base. The photodegradation rates of PAMs fitted a first-order kinetic model and their photodegradation rates decreased in the following sequences: pyrene>chrysene>benzo[a]pyrene among the PAHs used.