• Journal of the Korean Chemical Society
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• v.55 no.2
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• pp.313-316
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• 2011

• Ceramist
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• v.3 no.3
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• pp.58-70
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• 2000

뼈 결정과 같이 결정도가 낮은 탄산 인회석 결정의 화학조성 및 구조는 순수 수산화인회석 과 물리적 및 화학적 성질에 있어서 매우 다르다. 극미세 결정으로 결정도가 매우 낮은 불완전 결정이며, 결정 표면은 매우 반응성이 높은 이온으로 구성되어 있어 유기분자나 세포와 활발히 반응할 수 있다. 이와 같은 뼈 결정의 특성을 고형 기질 표면에 불완전 결정도 인회석 박막을 형성시켜 생체재료에 재현하였다. 이 박막에는 뼈세포들이 잘 부착하였는데 특히 골모세포의 부착, 증식, 분화를 촉진하여 장차 이와 같은 뼈 탄산 인회석의 특성을 갖는 인회석을 생체이식 재료로 이용하므로써 우리 몸의 생리에 좀 더 가까운 인공 매식체를 개발할 수 있을 것으로 기대된다.

• Journal of the Korean Chemical Society
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• v.47 no.3
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• pp.297-300
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• 2003

• Journal of the Korean Chemical Society
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• v.46 no.5
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• pp.489-492
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• 2002

• Journal of the Korean Chemical Society
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• v.47 no.2
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• pp.183-188
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• 2003

• Proceedings of the Membrane Society of Korea Conference
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• 1993.04a
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• pp.31-32
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• 1993

본 연구는 내열성, 내약품성, 내유기용매성 등 물리, 화학적 성질이 우수한 PSF(Polysulfone)와 PI(Polyimide)계의 고분자를 화학적 개질을 통하여 친수성을 높히는 목적으로 술폰화 반응을 시켰다. 이러한 이온성이 부가된 PS와 PI막의 제조와 투과 특성을 측정 조사하였다.

• Journal of the Korean Chemical Society
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• v.25 no.3
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• pp.166-171
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• 1981

The reactions of trimethylbenzenes were investigated over dealuminated, cation-exchanged mordenite catalysts. Higher reaction temperature favored the formation of disproportionation products. In the reaction of 1,2,4-trimethylbenzene, the formation of 1,3,5-trimethylbenzene and the disproportionation products decreased sharply with reaction time. The product distribution, especially the distribution of trimethylbenzenes, suggests that the effective pore diameter of Ba-exchanged dealuminated mordenite catalysts lies somewhere between 8.1 and 8.6${\AA}$.

• Proceedings of the Korean Institute of Industrial Safety Conference
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• 1997.05a
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• pp.55-58
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• 1997

대기오염의 주요원인은 소각로 연소가스와 자동차의 배기가스로 이들 이동 오염원에서 배출되는 오염가스는 일산화탄소, 탄화수소, 질소 및 황산화물 둥이고 이들은 공기중의 산소와 반응하여 광화학반응을하여 오존을 생성하며 기타 미세먼지, 수분과 반응하여 스모그를 생성하여 인체의 호흡기 계통 질병을 유발케한다. (중략)

• KSBB Journal
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• v.17 no.6
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• pp.543-548
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• 2002

The enantioselective esterification of racemic ibuprofen catalyzed by a Candida rugosa lipase was studied according to reaction conditions such as a lipase concentration, reaction temperature, alcohol chain length and alcohol concentration. The S-(+)-ibuprofen alkyl esters prepared were converted to S-(+)-ibuprofen by hydrolysis with sulfuric acid as a catalyst. High conversions in the esterifications were obtained at 60$^{\circ}C$ and an equimolar ratio of octanol to ibuprofen. The initial reaction rate of the esterification decreased with increasing octanol concentration. Conversion and initial reaction rate increased with increasing alcohol chain length. Values of enantiomeric excess(ee) according to esterification reaction conditions did not change below 60$^{\circ}C$. On the other hand, values of conversion and ee for the chemical hydrolysis of S-(+)-ibuprofen alkyl esters were independent of alcohol alkyl chain length. Optical resolution of racemic ibuprofen was achieved by lipase catalyzed esterification and chemical hydrolysis. The separation method provided a high yield and enantioselectivity for the production of S-(+)-ibuprofen from racemic ibuprofen.

• Journal of the Korean Chemical Society
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• v.41 no.10
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• pp.541-546
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• 1997

Manganese dioxide may react with silicon tetrachloride to form manganese(Ⅳ) oxodichloride which reacts subsequently with another molecule of silicon tetrachloride leading to manganese tetrachloride eventually in chlorinated solvents. This in situ generated manganese(Ⅳ) oxodichloride or manganese tetrachloride were found to be very effective for the chlorination of a wide variety of alcohols to the corresponding chlorides. Primary, secondary and benzylic alcohols were converted into corresponding chlorides when treated with silicon tetrachloride in the presence of manganese dioxide at room temperature.