• Bulletin of the Korean Chemical Society
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• 제21권6호
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• pp.583-587
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• 2000

Depletion kinetics of ground state FeO molecules by $0_2$, $N_2O$ and $N_2$ has been studied at room temperature. The ground state FeO molecules were generated by photolysis of a $Fe$(CO)_5$/M(O_2$, $N_2O)/He$ mixture using an unfocused weak UV laser beam. The formation of ground state FeO molecules was identified by a laser-induced fluorescence (LIF) method. The intensity distribution of those undisturbed rotational lines suggests that the rotational temperature of the ground state FeO molecules is lower than room temperature. The LIF intensities of FeO molecules at different partial pressures of $0_2$, $N_2O$ and $N_2$ were monitored as a function of the time delay between the photolysis and probe laser pulses to obtain the depletion rate constants for the ground state FeO. They were 1.7+ 0.2x $10^{-12}$, 4.8 $\pm0.4$ x $10^{-12}$, and $1.4\pm$ 0.2x $10^{-12}cm^3$molecule^{-1}s^{-1}$$ by $0_2$, $N_20$, and $N_2$, respectively.

• 청정기술
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• 제23권1호
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• pp.95-103
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• 2017

본 연구는 비 $TiO_2$ 계 광촉매 중 가장 널리 알려져 있는 $ATiO_3$ (A = Ca, Sr, Ba) perovskite를 sol-gel 법을 이용해 합성하였고, 골격치환이 용이한 점을 이용해 A site에 Ni을 첨가한 입자를 합성하였다. 합성한 $ATiO_3$와 Ni-$ATiO_3$ 입자의 불리화학적 특성은 X-선 회절분석(XRD), 자외선-가시선 분광광도계(UV-visible spectroscopy), 주사전자현미경 (SEM), 에너지분산형 분광분석법(EDS), 질소 등온 흡 탈착실험, X선 광전자분광법(XPS)을 이용해 확인하였다. 수소제조는 메탄올을 광분해하여 얻었으며, $ATiO_3$ 보다 Ni-$ATiO_3$ 촉매에서 높은 수소발생량을 나타내었다. 특히 Ni-$SrTiO_3$ 촉매를 사용하였을 때 24시간 반응 후 $273.84mmolg^{-1}$의 수소가 발생하였다. 또한 Ni-$SrTiO_3$ 촉매는 물(0.1 M KOH)을 분해하였을 때에도 높은 수소 제조 성능을 나타냈으며, 24시간 반응 후 $961.51mmolg^{-1}$의 수소가 발생한 것을 확인하였다.

• 한국환경과학회지
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• 제15권11호
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• pp.1061-1067
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• 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.

• 한국환경과학회지
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• 제15권7호
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• pp.669-676
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• 2006

PAHs are major pollutants that are widely distributed in soil and groundwater environment, so that may be regarded as carcinogens. We investigated the degradation kinetics of PAH in aqueous solution when low pressure UV energy and ultrasonic irradiation were applied. Phenanthrene and pyrene were used as model compounds. The degrees of degradation of these compounds with time were analyzed with a GC/MSD (SIM-mode). UV photolysis experiments showed that phenanthrene was reduced by 90 -67% at initial concentrations of 1 ppm to 8ppm whilst it decreased to 50% at 10 ppm. Under the same conditions pyrene was degraded up to about 75% at lower initial concentrations but the reduction efficiency dropped to a level of 34 to 29% at the higher concentrations above 8 ppm. The reaction orders for phenanthrene and pyrene were found to be zero-th and ca. -0.4th order, respectively, thus implying that the reported assumption of pseudo 1st order reaction for some PAHs would be no longer valid. PAH degradation was roughly proportional to the intensity of UV (number of lamps), exhibiting maximum 92.5% of the degradation efficiency. The solution pH was lowered to 4.4 from 6.4 during the experiments partially because the carbons decomposed by the energy reacted with oxygen radicals to produce carbon dioxides. Ultrasonic irradiation on phenanthrene solutions gave relatively poor results which matched to 50 to 70% of degradation efficiency even at 2 ppm of initial concentration. Phenanthrene was found to be degraded more efficiently than pyrene for the two energy sources. Ultrasound also followed the same reaction kinetics as UV energy on PAH degradation.

• 대한화학회지
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• 제37권4호
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• pp.453-461
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• 1993

테프론 코일과 저압 수은 램프를 사용, 간단하게 제작된 광화학 반응기를 이용한 HPLC 검출 방법을 연구하였다. 4종의 티오카바메이트 시료들을검출함에 있어 UV, 형광 및 전기화학 검출기 등에서 광화학 반응을 통한 액체 크로마토그래피 후컬럼 검출법의 유용성을 알아보았다. 액체 크로마토그래피를 통해 분리된 티오카바메이트류에 254nm의 UV을 조사할 경우 4종의 시료는 모두 광반응이 일어나 형광을 통해 분리된 티오카바메이트류에 254nm의 UV을 조사할 경우 4종의 시료는 모두 광반응이 일어나 형광을 나타내거나, 전기화학 검출기에 큰 검출 응답을 나타내었다. UV 검출법의 경우 광반응 생성물은 광반응전보다 검출감도는 감소하였으나 장파장쪽에서 검출이 용이하였다. 형광 검출법의 경우 광반응전 4종의 티오카바메이트는 전혀 검출되지 않았으나, 광반응 후 MPTC,CPTC는 Ph 4.0, 50% 아세토니트릴 이동상 조건에서 5.0~9.3ng의 검출한계를 나타내었다. 전기화학 검출법에서는 광반응전 시료가 매우 작은 검출 응답을 보였고, 광반응 후 시료는 5~20배 이상의 검출감도가 증대되었으며 13.3~0.02ng의 검출한계를 나타내었다. 이때 최적 검출조건은 50% 아세토니트릴 $-0.5{\times}10^{-2}$ M 인산 완충용액, pH 7.0 이었다. 또한 티오카바메이트의 광반응물과 OPA-MERC를 반응 코일내에 유도체를 형성시켜 형광검출기로 검출해냄으로써 광분해물에서 1차 아민이 생성됨을 알 수 있었다.

• Biomolecules & Therapeutics
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• 제3권2호
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• pp.149-153
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• 1995

Nitric oxide (NO) has been regarded as one of the neurotransmitters of nonadrenergic, noncholinergic (NANC) nerve stimulation in rabbit corpus cavernosum, rat gastric fundus and human intestine. PIANO (photo-induced adequate nitric oxide) is a very useful tool to investige the role of NO in various smooth muscles where NO is a mediator. The present study was undertaken to compare the physiological responses of the rat gastric smooth muscle in response to NANC nerve stimulation and to PIANO. Photolysis of L-NAME, D-NAME and streptozotocin (572) by UV light in the bathing medium caused relaxation of rat gastric fungus that contracted with carbachol, but was resistant to tetrodotoxin (TTX, 1 $\mu$M). Electrical stimulation (20 V, 2~32 Hz, 0.2 msec, 10s) of the gastric fundus, in the presence of atropine and guanethidine, induced frequency-dependent, TTX-sensitive relaxation. Sodium nitroprusside (1 nM-10 $\mu$M), a NO donor, mimicked the relaxations observed after NANC-stimulation or PIANO. Furthermore, PIANO caused UV light exposure time-dependent increase of CGMP in rat gastric fungus strips. These results provide another evidence indirectly that NO is one of the mediators of the NANC inhibitory nerve stimulation in the rat gastric fundus.

• Journal of Photoscience
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• 제9권2호
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• pp.138-141
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• 2002

A photo-labile compound which is bioinactive but, upon irradiation with light, yields bioactive species is called as "caged compound". Photolysis of caged compounds generating bioactive species, has become a general method to produce a desired amounts of bioactive species in the specific time interval at the desired place or area of the target biological systems. For this purpose, we designed and synthesized caged hydroxyl radical., "Photo-Fenton Reagent" NP-IIl. NP-IIl has a strong absorption maximum at 377 nm and yields hydroxyl radicals upon UV light irradiation. The antioxidant activity of the ${\alpha}$ -lipoic acid and other naturally occurring compounds has been examined by using NP-IIl as a molecular probe. For example, upon photoirradiation of NP-lII with BSA or apolipoprotein of human low density (LDL), the significant oxidative modifications were observed in both cases. The oxidation was completely suppressed in the presence of ${\alpha}$-lipoic acid, which clearly demonstrates the strong hydroxyl radical scavenging activity of ${\alpha}$-lipoic acid. Other applications of NP-lII will also be described

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1990년도 제2차 학술발표초록집
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• pp.67-67
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• 1990

Three non-ionic and two anioinic spin probes, differing in size and substituent, were synthesized. Their mobility in dried nylon 6 film was investicated by the spin probe technique using electron spin resonance spectrometer. When the size of a spin probe was large and the interaction between the probe molecules and polymer chains existed, the mobility of spin probes decreased. From Arrhenius plots of rotational correlation time, one discontinuity point ($T_d$) was determined. The activation energies for rotation below and above $T_d$ were discussed in terms of the mode of probe rotation. Three spin probes could be viewed as azo dyes having a built-in nitroxide radical. Photolysis of them in dimethylformamide and in nylon 6 film was performed by exposure to 254 nm UV light in the presence of air. It was found that dyes having a built-in nitroxide radical showed better photostability than dyes derived from ${\bata}-naphthol$..

• E2M - 전기 전자와 첨단 소재
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• 제9권1호
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• pp.59-66
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• 1996

Polyimides containing cyclobutane ring in main chain is known to be thermally stable and able to be developed in organic solvents after photolysis with 254 nm UV light. This type of polyimides can be used as promising positive photoresist in VLSI fabrication process. In the current VLSI process, photoresist films are formed by spin coating. The film thickness is more than several hundred nano meters. It seems that there is room for improvement of film coating process by introducing Langmuir Blodgett technique. Thereby ultra thin film photoresist can be formed, and higher density of integration in VLSI be achieved. In the present work, depositing procedure of LB films of this polyimide was investigated. LB film thickness was measured by ellipsometry to evaluate deposited film status. Chemical imidization procedure was studied to avoid several problems in thermal imidization. The pattern of submicron dimension has successfully formed on LB film of 8nm thick, which found showing good contrast.

• Journal of Photoscience
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• 제6권3호
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• pp.145-151
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• 1999

The use of O-carbamoyloximes as photobase generators was investigated. $\alpha$-Meth-ylbenzilydeneamino phenylcarbamate(2a) and $\alpha$-methyl benzilydeneamino cyclohexylcarbamate(2b) were prepared by the reaction of phenyl or cyclohexyl isocyanates with acetophenone oxime , respectively. Aniline, phenylhydrazine and N, N'-diphenylhydrazine were detected in thephotolysis of 2a and cyclohexylamine and cyclohexylhydrazine in the photolysis of 2b. A monomer having pendant carbamoyloxyimino groups (BGM) was prepared by the reaction fo methancryloyloxyethyl iocyanate with acetophenone oxime, and copolymerized with styrene. The BGM copolymer films turned insoluble on UV irradiation, and the degree of insolubilizationwas increased by post-baking. The photocrosslinking was thought to be due to coupling of resulting pendant aminyl radicals, and the thermal crosslinking was due to association of resulting amino and hydrazino groups by hydrogen bonding. The introduction of epoxy groups into polymer increased the degree of thermal crosslinking by post-baking.