• Journal of Technologic Dentistry
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• v.33 no.4
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• pp.291-297
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• 2011

Purpose: The purpose of this study was to know the availability of three photosensitizers, CQ, PD, DA, as a photosensitizer of dental resin composite. We want to know abortion band around visible light region for the using potential possibility as a photosensitizer for visible light cured dental composite resin. And I studied to know the relative photodecomposition ratio of three photosensitizers with or without photoinitiator, DAEM. Methods: The photodecomposition of three photosensitizers were studied by UV absorption spectroscopy in ethanol and determined by same instrument with irradiation time for relative photodecomposition. In order to study the effect of amine on photodecomposition was added the DAEM in the photosensitizer solution and the relative rate was measured by the same procedure with aove mentioned. Results: The all of three photosensitizers are absorbed around visible light region. The relative rate of decrease in absorbance incereased in the order: CQ < BD < PD. The effect of DAEM on the photodecomposition of the photosensitizers was appeared different results without DAEM. The photodecomposition rate of PD and DA decreased somewhat with the addition of amine, while that of CQ increased. The rtealtive photodecomposition rate increased in the oprder: BD ${\leq}$ CQ < PD with the addition of amine, but the differnce was not significant. Conclusion: PD and DA like CQ gives to the possibility of use as a photosensitizer for visible light cured dental composite resin by absorption around visible light region and photodecomposition in the maximum absorption wavelength. And it is showed that PD and DA are not effective decomposed with amine initiator, DAEM but CQ decomposed with DAEM effectively. This result may be due to a different mechanism operating for the decomposition of photosensitizers in the presence of amine.

• Journal of Photoscience
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• v.9 no.2
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• pp.403-405
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• 2002

To study photocatalytic mechanism of metal doped $Ti0_2$, we investigated photodecomposition effect, photocurrent effect and antibacterial effect. When aluminium content was 2 wt %, photodecomposition effect was better than the others. Silver doped thin films had high photocurrent efficiency and antibacterial effect. This reactions were caused by dissolved oxygen in solution and oxygen adsorbed on surface of thin films.

• Journal of Environmental Science International
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• v.25 no.3
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• pp.373-383
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• 2016

The aim of this study is to determine the exposure concentration of tetrabromobisphenol A(TBBPA) in southwestern coast and their photodecomposition rate. Also, it is to identify the radical species of the photodecomposition of TBBPA and their reactive byproducts using the electron spin resonance(ESR) method. TBBPA was not detected in any of the sea water samples from Mokpo, Gunsan, or Goheung. The sediment samples from Mokpo contained not detection(N.D)~50.0 ng/g dry wt., while those from Gunsan contained N.D~28.5 ng/g dry wt. and those from Goheung contained N.D~7.3 ng/g dry wt. The photodecomposition rates were $2.56{\times}10^{-6}/hr$ by visible light(400 nm), $7.98{\times}10^{-6}/hr$ by ultraviolet light(300 nm <), and $6.78{\times}10^{-6}/hr$ by sunlight. Also, we confirmed that singlet oxygen and hydroxyl radicals are the key reactive oxygen species at wavelengths greater than 400 and 300 nm, respectively. This study shows that the main byproducts formed during irradiation at wavelengths above 300 nm are 2,6-dibromobenzosemiquinone radical(2,6-$DBSQ{\cdot}^-$) and g-value 2.0048 doublet spectrum.

• Korean Journal of Microbiology
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• v.10 no.1
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• pp.35-40
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• 1972

1) The photodecomposition rate of guanine being catalized by methylene blue ws 53.7% in contrast with 9.3% that of dark control for 180 min. 2) In guanine control, the decomposition rate was very low. For 180 min., the rate was 8.1% in illuminated sample and 3.9% in non-illuminated sample. 3) The decomposition rate of methylene blue was obviously interfered by the existence of guanine. In guanine and methylene blue mixture solution, the net decomposition rate, excluding that of dark control ws 39.2% and in dye only solution, it was 48.5%.

• Bulletin of the Korean Chemical Society
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• v.16 no.1
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• pp.47-52
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• 1995

The mechanism of the photodecomposition of 2-methoxy-1,2-diphenyl diazoethane has been investigated in methanol and isoprene using time-resolved laser flash photolysis techniques. The reaction of triplet carbene which is generated from 2-methoxy-1,2-diphenyl diazoethane with methanol is believed to proceed via thermal excitation to the singlet state. The activation energy and enthalpy are consistent with a mechanism involving thermal equilibrium between the triplet and singlet state followed by the reaction of the singlet with methanol to give ether.

• Textile Coloration and Finishing
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• v.32 no.3
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• pp.158-166
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• 2020

Self-cleaning fabric is a fabric having a function of decotamination via photodecomposition of photocatalyst or wash-off of contaminants on the superhydrophobic surface. TiO₂ is the main photocatalyst for this purpose, but it only functions under UV light which is only a little portion of sunlight, compared to visible light. In this regard, this study aims to investigate Fe-doped TiO₂ for improved photodecomposition from visible light sensitization to apply self-cleaning finishing of PET fabrics. Moreover, the Fe-doped TiO₂ treated PET fabric was further treated with hexadecyltrimethoxysilane to provide superhydrophobicity on the PET fabrics. As a result of this dual treatment, the prepared fabric exhibited excellent photodecomposition of methylene blue with 96.96% in 12h under sunlight and superhydrophobicity with water contact angle of 166.5° and roll-off angle of 7°. This suggested that the excellent self-cleaning functions can be privided to PET fabric via Fe-doped TiO₂ and hexadecyltrimethoxysilane treatment.

• Proceedings of the Korean Vacuum Society Conference
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• 2003.08a
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• pp.112-112
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• 2003

• Journal of Korean Society for Atmospheric Environment
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• v.17 no.4
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• pp.363-370
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• 2001

In this study, TiO$_2$, the popular photocatalyst, was used to decompose ethanol. TiO$_2$was prepared by the sol -gel method and coated on pyrex stick. A 15W, UV-A lamp was used as the UV light source and il gas chromatography (HP 5890) was used to confirm the concentrations of ethanol, $CO_2$and the intermediates. Variation of preparation parameters and calcination temperature for TiO$_2$photocatalysts in the sol -gel method caused changes of ethanol decomposition activity. The best ethanol photodecomposition activity was obtained on the sample when prepared with 0.14 mol of HCI, a mol of ethanol and 1.3 mol of TTIP ware mixed in sol-gel process and calcinated at 50$0^{\circ}C$ for 3 hours. Acetaldehyde was detected as an intermediate and decomposed to carbon dioxide and water at the end of the reaction.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 1994.04a
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• pp.93-93
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• 1994

• Bulletin of the Korean Chemical Society
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• v.1 no.3
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• pp.93-97
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• 1980