• Transactions on Electrical and Electronic Materials
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• 제11권1호
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• pp.1-10
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• 2010

This is an overview paper reporting our most recent work on processing and microstructure of nano-structured oxides and their photoluminescence and photo-catalysis properties. Zinc oxide and related transition metal oxides such as vanadium pentoxide and titanium dioxide were produced by a combination of magnetron sputtering, hydrothermal growth and atmosphere controlled heat treatment. Special morphology and microstructure were created including nanorods arrays, core-brushes, nano-lollipops and multilayers with very large surface area. These structures showed special properties such as much enhanced photoluminescence and chemical reactivity. The photo-catalytic properties have also been promoted significantly. It is believed that two factors contributed to the high reactivity: the large surface area and the interaction between different oxides. The transition metal oxides with different band gaps have much enhanced photoluminescence under laser stimulation. Use of these complex oxide structures as electrodes can also improve the energy conversion efficiency of solar cells. The mixed oxide complex may provide a promising way to high-efficiency photo emitting materials and photo-catalysts.

• Nuclear Engineering and Technology
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• 제46권2호
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• pp.183-194
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• 2014

Recently, a CANDU digital reactivity computer system (CDRCS) to measure the worth of the liquid zone controller in a CANDU-6 was developed and successfully applied to a physics test of refurbished Wolsong Unit 1. In advance of using the CDRCS, its measureable reactivity range should be investigated and confirmed. There are two reasons for this investigation. First, the CANDU-6 has a larger reactor and smaller excore detectors than a general PWR and consequently the measured reactivity is likely to reflect the peripheral power variation only, not the whole core. The second reason is photo neutrons generated from the interaction of the moderator and gamma-rays, which are never considered in a PWR. To evaluate the limitations of the CDRCS, several tens of three-dimensional steady and transient simulations were performed. The simulated detector signals were used to obtain the dynamic reactivity. The difference between the dynamic reactivity and the static worth increases in line with the water level changes. The maximum allowable reactivity was determined to be 1.4 mk in the case of CANDU-6 by confining the difference to less than 1%.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2004년도 Asia Display / IMID 04
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• pp.1169-1172
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• 2004

Polyimides are blended with photoreactive polymers in order to improve the thermal stability of molecular orientation of photoreactive groups induced by polarized UV irradiation. The polyimide/photopolymer blends can be applied for the photo-induced liquid crystal alignment layers. However, the polyimides are also decomposed by UV irradiation and this may have the negative effect on the orientation of liquid crystals. In order to elucidate the influence of polyimide on the molecular orientation of liquid crystal, non-photoreactive naphthalenic polyimide (1,4,5,8-naphthalene tetracarboxylic dianhydride} was selected for the blend alignment layers. We prepared the blends of photo-reactive coumarin polymers and naphthalenic polyimide, and investigated the orientation of liquid crystals. Thermal stability of the orientation of liquid crystals was enhanced due to the thermally stable polyimide. However, there was no other side-effect of polyimide on the orientation of liquid crystals and this might be attributed to the non-photo-reactivity of naphtahlenic polyimide.

• Bulletin of the Korean Chemical Society
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• 제30권3호
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• pp.679-682
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• 2009

Utilizing a planar five coordinating N3S2 ligand, 2,6-bis(2-methylthiophenyliminomethyl)pyridine, a pseudo 7-coordinated manganese(II) complex with two labile triflate anions in the axial positions was synthesized. The reaction of the manganese(II) complex with an oxidant, iodosylbenzene, produced a metastable high-valent manganese(IV)-oxo species at 0 ${^{\circ}C}$. The high-valent Mn(IV)-oxo intermediate was characterized with a UV-vis spectrophotometer and an electrospray ionization mass spectroscopy. Reactivity studies of the Mn(IV)=O species revealed that the intermediate is capable of oxygenating $PPh_3$ and N-dealkylating N,N-dimethyl-toludine.

• 한국전기전자재료학회논문지
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• 제29권6호
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• pp.327-331
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• 2016

Resistive random access memory (ReRAM) of metallic conduction channel mechanism is based on the electrochemical control of metal in solid electrolyte thin film. Amorphous chalcogenide materials have the solid electrolyte characteristic and optical reactivity at the same time. The optical reactivity has been used to improve the memory switching characteristics of the amorphous $As_2Se_3$-based ReRAM. This study focuses on the formation of holographic lattices patterns in the amorphous $As_2Se_3$ thin film for straight conductive channel. The optical parameters of amorphous $As_2Se_3$ thin film which is a refractive index and extinction coefficient was taken by n&k thin film analyzer. He-Cd laser (wavelength: 325 nm) was selected based on these basic optical parameters. The straighten conduction channel was formed by holographic lithography method using He-Cd laser.$ Ag^+$ ions that photo-diffused periodically by holographic lithography method will be the role of straight channel patterns. The fabricated ReRAM operated more less voltage and indicated better reliability.

• 한국응용과학기술학회지
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• 제34권2호
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• pp.203-209
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• 2017

양이온계 광중합에 적용 가능한 propenyl ether 형태의 단량체들을 mono 및 di-functional alcohol과 allyl bromide의 축합반응으로 합성하였다. 이들 단량체들을 양이온 광개시제와 혼용하여 코팅조성물을 제조하여 광경화 반응성을 조사하였다. 그 결과 mono propenyl ether 형태인((prop-1-en-1-yloxy)methyl)benzene (POMB)는 dipropenyl ether 계인 1,4-bis(prop-1-en-1-yloxy) benzene (BPOB) 비교하여 초기 중합 속도는 10.2로 상대적으로 낮게 나타났으나 1.5mol%의 광개시제를 포합한 배합물에서는 90초이내에 거의 정량적으로 반응하였다. 또한 긴알킬기를 갖는 술폰산 염계 광개시제들은 단량체들에 빠른 용해 특성을 나타내었고 산성도가 높은 광개시제인(4-n-decyloxyphenyl)diphenylsulfonium hexafluoroantimonate(DPSA)와 (4-n-decyloxyphenyl) diphenylsulfonium triflate (DPST)를 사용한 경우 비교적 높은 중합속도와 전환율을 나타내었다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제11권6호
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• pp.69-75
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• 2006

지하 저장 탱크로부터의 유류 유출로 인하여 전세계적으로 넓은 지역의 토양 및 지하수가 오염되고 있다. Methyl tert-butyl ether(MTBE)는 대기 오염 감소를 위하여 널리 사용되고 있는 유류 첨가제이지만 토양 및 지하수로 유입되어 섭취 되었을 때 발암 가능성이 있는 유독 물질이다. 본 연구는 고도 산화 처리 기법 중 유기 오염물의 분해에 높은 효율을 나타내는 고전적 Fenton reaction의 최대 단점인 강한 산성(pH 2.5-3) 의존성을 극복한 새로운 산화 처리 기법을 개발하여 고농도의 MTBE를 효과적으로 분해 하는 것을 그 목적으로 하여 자연 친화적인 chelating agents를 사용하여 중성 영역에서 Fenton reaction을 가능하게 하는 기법인 Modified Fenton reaction과 Ultra Violet light(UV)를 이용하여 분해효율을 극대화 하는 Photo-assisted Fenton reaction을 응용한 Modified Photo-Fenton reaction system을 개발하여 최적 반응 조건 및 반응 차수, 반응 메커니즘을 밝혀내었다. 낮은 독성과 높은 생분해성을 나타낸 Citrate ion을 chelating agents로 선정하였으며 최적 반응 조건은 [$Fe^{3+}$] : [Citrate] = 1 mM : 4 mM, 3% $H_2O_2$, 17.4 kWh/L UV dose, 초기 pH 6.0이며 이 조건에서 1000 ppm MTBE를 분해한 결과 6시간 후 86.75%, 16시간 후 99.99%의 높은 분해율을 나타냈으며 최종 pH는 6.02로 안정적이었다. 또한 Modified Photo-Fenton reaction을 이용한 MTBE 분해 반응은 유사 1차 반응을 나타내었으며 methoxy group이 ${\cdot}OH$ radical과 주로 반응하여 tert-butyl formate(TBF)가 주요 분해 산물이 되는 분해 경로를 따른 다는 것이 밝혀졌다. 본 연구로 개발된 Modified Photo-Fenton reaction에서 발생되는 산화제인 ${\cdot}OH$ radical의 비선택적 반응성을 고려할 때 본 system은 다른 종류의 유기 오염물 분해에도 효과적일 것으로 판단된다.

• Korean Chemical Engineering Research
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• 제43권1호
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• pp.1-8
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• 2005

본 연구에서는 광촉매의 광자효율을 증가시키고, 물성을 변화시켜 광촉매 성능을 향상시키기 위하여, 자동차 폐 촉매에서 추출된 귀금속 용액 또는 $H_2PtCl_6$ 용액을 수열합성법에 의해 제조된 $TiO_2$와 상업용 $TiO_2$인 P-25(Degussa Co.)를 함침시켜 변조된 광촉매를 제조하였다. 그리고 변조된 광촉매는 ICP-AES, EDS, UV-DRS, XRD, XANES, SEM에 이용하여 물성분석 하였다. 그리고 폐 자동차 촉매전환기의 추출용액을 함침시킨 광촉매를 변조하여 band-gap energy를 1.76eV(705 nm)의 가시광 영역까지 조절하였다. 변조된 광촉매는 PVC가 주성분인 벽지 코팅제와 농도별로 혼합하여 광화학반응을 위한 기능성 도료를 제조하였다. 이 도료를 사용하여 광촉매가 코팅된 기능성 벽지를 제조하였으며, 제조된 벽지의 광촉매 성능을 평가하였다. 반응모델 물질로 NO를 이용하여 촉매 조성, 반응물 농도, 벽지의 촉매 담지량, 반응시간에 따른 광 화학반응속도를 측정하였다. 그 결과 폐 자동차 촉매전환기의 추출용액으로 변조된 $TiO_2$의 광촉매 활성이 크게 증가하였음을 알 수 있었고 그 중에서도 P-25에 추출용액을 함침시킨 P-25(w)의 광촉매가 가장 우수한 광촉매활성도를 나타내었다.

• Bulletin of the Korean Chemical Society
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• 제25권1호
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• pp.45-50
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• 2004

$Cu^{II}$-complexes of N-salicylideneaniline and its derivatives were not light sensitive in most solvents such as acetonitrile. A photo-decomposition occurred upon irradiation in halocarbon solvents such as $CHCl_3$. It has been suggested that such photoreactivity is attributed to the reactivity of charge-transfer to solvent (CTTS) excited state attained upon irradiation. A mechanism has been proposed to account for the results obtained. The complexes have been thermally analysed in nitrogen and static air using thermogravimetry (TG) and derivative thermogravimetry (DTG). The thermal degradation of the complexes proceeds in two or three stages. The kinetic parameters obtained from the Coats-Redfern and Horowitz-Metzger equations show the kinetic compensation effect.

• Bulletin of the Korean Chemical Society
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• 제11권3호
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• pp.241-244
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• 1990

The photochemistry of 1-Methyl-2-cyclohexenyl aryl ketones (phenyl ketone 7a, p-toluyl ketone 7b, biphenyl ketone 7c and -naphthyl ketone 7d) is reported. The aryl ketone 7a, 7b and 7c undergo photo-racemization with efficiencies of 0.75, 0.79 and 0.76 respectively on direct irradiation. Direct irradiation of the ketone 7d, however, undergoes 1,3-shift with an efficiency of 0.02. Triplet states are responsible for the racemizations and singlet state is responsible for 1,3-shift as in general. The ketone 7a, 7b and 7c are good example of a few ${\beta},{\gamma}$-unsaturated ketones which undergo efficient intersystem crossing on direct irradiation.