• Korean Journal of Environmental Agriculture
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• v.6 no.1
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• pp.17-24
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• 1987

Benzene-ring-labelled $^{14}C-Bentazon$(3-isopropyl-2, 1, 3-benzothiadiazin-4-one-2, 2-dioxide) incubated aerobically in a German and a Korean soil at application rates of 5.51 and 25.05mg/Kg was mineralized to $^{14}CO_2$ at average rates of 0.6% and 0. 2%/week, respectively, in both soils, in the absence of plants. Distilled water was the most suitable solvent for the extraction of Bentazontreated soils. Extraction results disclosed that higher percentages of nonextractable residues were formed in the lower concentration of 5.51mg/Kg than in the higher concentration of 25.05mg/Kg, relative to the initial concentrations.

• Analytical Science and Technology
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• v.21 no.5
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• pp.403-411
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• 2008

Dimethyldibutyltetradecylmalonamide (DMDBTDMA) extractant was used in a solvent extraction process for a radioactive liquid waste treatment. For the study of radiolysis phenomena, DMDBTDMA was synthesized and the degradation compounds (n-methylbutylamine, tetradecane, 1-tetradecanol) in the DMDBTDMA extractant, irradiated with $^{60}Co$ gamma ray, were identified and determined as radiolysis products by a Fourier transform infrared (FT-IR), gas chromatograph/mass spectrometer (GC/MS) analysis and GC/MS with selected ion monitoring (SIM) mode. Retention behavior of n-methylbutylamine, n-dodecane, tetradecane and 1-tetradecanol in the total ion chromatogram with the standard materials and n-dodecane as the internal standard (ISTD) were 2.35 min., 8.83 min., 10.68 min. and 12.75 min., respectively. In the case of tetradecane, there was a linear relationship between the concentration of the tetradecane and the absorbed dose of the ${\gamma}$-ray irradiated DMDBTDMA.

• Journal of the Korean Chemical Society
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• v.24 no.5
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• pp.347-355
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• 1980

The rate constants for the reaction of ${\alpha}$-naphthalene carbonyl chloride and ${\beta}$-naphthalene carbonyl chloride have been determined in methanol-acetonitrile and methanol-acetone. The rate constant of ${\alpha}$-naphtalene carbonyl chloride is higher than that of ${\beta}$-naphthalene carbonyl chloride. This behavior is consistent with Dewar's number, Nr and also Streitwieser's value ${\sigma}^+$. Since in the transition state carbonyl carbon is transformed to$sp^3$, no peri-hydrogen effect was observed.

• Journal of the Korean Chemical Society
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• v.41 no.9
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• pp.443-448
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• 1997

Kinetics for the solvolyses of acyl chlorides and alkyl chlorides in hydroxylic solvent mixtures have been measured by conductometric method at various temperatures and pressures. The activation parameters (${\Delta}V^{\neq},\; {\Delta}H^{\neq},\; {\Delta}S^{\neq}$) were estimated from the rate constants. The reactivities of these reactions were also estimated from the correlation of the activation volumes with the activation entropies.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2002.05b
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• pp.459-460
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• 2002

현재 오염 토양의 복원기술은 여러 가지 문제점들을 안고 있어 보다 경제적이면서 신속하고 실용적인 오염물질 제거방법의 개발이 요구되고 있다. 이에 본 연구에서는 유류에 오염된 토양을 극초단파와 용매를 사용하여 복원하는 것에 관한 기초 조사를 위한 실험을 수행하였다. 그 결과 유류에 오염된 토양을 극초단파를 이용하여 정화를 할 경우 토양 입자의 크기도 고려를 하여야 할 것으로 사료된다. 그리고, soxhlet 추출법과 극초단파 추출법을 비교하였을 경우 soxhlet 추출법에 비하여 약 1/3 정도의 용매로 추출이 가능하며, 1분 내ㆍ외의 추출 시간으로 soxhlet 추출법에 의한 kerosene의 회수율과 유사하거나 또는 그 이상의 회수율을 얻을 수 있는 것으로 조사되었다.

• Journal of Life Science
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• v.2 no.2
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• pp.120-131
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• 1992

효소에 의한 펩티드합성법은 합성반응의 개발초기에는 용매로서 침전계를 이용하여 아미노산 혹은 펩티드기질에서 펩티드생성의 방향으로 평형화하는 방법을 많이 이용하였지만 최근에는 물에 섞이는 유기용매들을 수용액과 함께 사용하여도 합성반응이 이루어진다는 사실이 밝혀졌다. 하지만, 효소를 공업적으로 이용할 때 값이 너무 비싸고 합성물과의 분리, 정제에 어려움이 있다. 이러한 문제를 해결하기 위하여 효소의 고정화법이 널리 이용되고 있다. 한편 protease에 의한 펩티드의 역합성은 단백질공학의 한 수법인 반합성으로서 주목을 끌고 있다. DNA의 조작기술이 오늘날과 같이 발전하기 이전에는 단백질합성의 공학적기법은 이 반합성과 화학적수식으로 한정되었다. 본고에서는 protease를 이용한 생리활성펩티드의 합성에 필요한 protease의 종류, 이들의 펩티드합성작용기구, 합성설계조건 및 유용 생리활성펩티드의 합성 예를 소개하였다.

• Journal of the Microelectronics and Packaging Society
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• v.2 no.1
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• pp.35-48
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• 1995

마이크로회로내에서 티탄산바륨 중 바륨의 일부가 납으로 치환됨에 따른 전기적 특 성의 변화를 확인하기 위하여 MOD(금속유기화합물 분해법)공정에 의 barum 2-ethylhexanoate, barium neodecanoate, lead 2-ethylhexanoate 및 titanium dimethoxy 야 -2-ethylhexanoate 와 같은 MOC(금속 유기화합물) 들을 합성하고 공통 용매에 대한 용해 도를 시험하였다. 그 결과 barium 2-ethylhexanoate 만 p-xylene에 대한 용해도가 낮았으며 그 외의 다른 MOC들은 모두 p-xylene 단일 용매에 매우 잘 용해되었다. 바륨의 일부가 납 으로 치환된 티탄산 납바륨 박막은 MOC 혼합용액을 ITO/glass, Pt/SiO2/Si 및 Pt/Ti/SiO2/Si 웨이퍼 기판 위에 spin coating 하고 소성하여 얻었다. 이와 같이 얻어진 박막 의 전기적 특성을 측정하고 그 결과를 비교 고찰하였다.

• KSBB Journal
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• v.9 no.3
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• pp.306-311
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• 1994

Optical resolution of racemic ${\alpha}$-methylbenzylamine was carried out by using Bacillus licheniformis protease in organic media. Enantioselective amidation of racemic amino with an ester as an acyl donor was successfully employed to resolve the racemate. To enhance reaction rate and enantioselectivity, pH-adjustment by lyophilization of enzyme dissolved in buffer, colyophilization with salts or lyoprotectants, selection of solvents and molecular design of esters were investigated. The optimization of the resolution reaction achieved about 30-fold increase in initial reaction rate and about 12-fold increase in enantioselectivity, respectively.

• KSBB Journal
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• v.17 no.1
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• pp.68-72
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• 2002

Supercritical Carbon Dioxide was evaluated and optimized for the enrichment and fractionation of the essential oil and the bitter principles of hops, both of which contribute to the flavor of beer, Selected conditions of extraction(pressure, temperature and co-solvent) influenced the composition, the olfactory results and the colour of the extract. Optimal extraction conditions were 30 min, 1800 psia and $ >45^{\circ}C $ with co-solvent. Under these conditions, yield was 65% from brewer's yeast. The bittering substances from brewer's yeasts almost were removed.

• Journal of the Korean Chemical Society
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• v.18 no.1
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• pp.8-11
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• 1974

The solvolysis of p-substituted benzenesulfonyl chlorides $(substituents:p-H, p-Br, p-NO_2, p-OCH_3)$ in acetonitrile-water mixtures below 50 % of water content has been studied kinetically. Results show that Hammett plots give concaved curves but the mechanism is predominantly $S_N2$ and water acts both as nucleophile and general-base.