• 상하수도학회지
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• 제27권4호
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• pp.457-468
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• 2013

Based on the activated sludge model(ASM), a mathematical model which represents the aerobic sludge digestion by sequencing batch reactor(SBR) combined with ultrasonic treatment was composed and performed in this study. Aerobic digestion using sequencing batch reactor(SBR) equipped with ultrasound treatment was also experimented for the purpose of parameter calibration. Most of the presented kinetic parameters in ASM or ASM2 could be used for the aerobic digestion of sludge but the parameters related in hydrolysis and decay rate needed modification. Hydrolysis rate constant of organic matter in aerobic condition was estimated at $0.3day^{-1}$ and the maximum growth rate for autotrophs in aerobic condition was $0.618day^{-1}$. Solubilization reactions of particulate organics and nitrogen by ultrasonication was added in this kinetic model. The solubilization rate is considered to be proportional to the specific energy which is defined by specific ultrasound power and sonication time. The solubilization rate constant by ultrasonication was estimated at $0.202(W/L)^{-1}day^{-1}$ in this study. Autotrophs as well as heterotrophs also decomposed by ultrasonic treatment and the nitrification reaction was limited by the lack of autotrophs accumulation in the digester.

• 대한화학회지
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• 제17권4호
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• pp.269-274
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• 1973

${\alpha}$-Cyano-${\beta}$-Piperonylacrylic Acid의 가분해 속도상수를 자외선분광기를 사용하여 구하였으며 아울러 넓은 pH범위에 잘 맞는 반응속도식도 얻었다. 이 식에 의하면 넓은 pH범위에 잘 맞는 반응속도식도 얻었다. 이 식에 의하면 넓은 pH범위, 특히 종전에 잘 규명된 바 없는 산성용매 속에서의 반응 및 hydroxide ion의 촉매역활 등도 정략적으로 잘 설명할 수 있음을 알았다. 즉 pH4.0이하에서의 가수분해반응은 ${\alpha}$-Cyano-${\beta}$-Piperonylacrylic Acid에 물분자가 첨가되므로써 시작되며 pH $5.0{\sim}7.5$ 에서는 ${\alpha}$-Cyano-${\beta}$-Piperonylacrylic Acid와 ${\alpha}$-Cyano-${\beta}$${\alpha}$-Cyano-${\beta}$-piperonylacrylate anion에 물분자만이 첨가되며 pH 12.0 이상에서는 hydroxide ion만이 ${\alpha}$-Cyano-${\beta}$-piperonylacrylate anion에 첨가됨을 알았다.

• 한국막학회:학술대회논문집
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• 한국막학회 2004년도 Proceedings of the second conference of aseanian membrane society
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• pp.82-85
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• 2004

Microinterface of W/Omicroemulsion prepared by phosphatidylcholine was used as reaction media of hydrolysis of phosphatidylcholine by phospholipaseA$_2$. Phosphatidylcholine was used as an amphiphile and was acted as a substrate. Organic phase of W/Omicroemulsion in this study was prepared by mixed organic solvents i.e. 2,2,4-trimethylpentane (isooctane) as a main solvent and 1-butanol as a co-solvent. The effect of added 1-butanol was remarkable not only on reaction beginning but also on high reaction rate. The hydrolysis reaction was dramatically initiated when 1-butanol was injected into the running isooctane/PC system. The enhancement by 1-butanol addition into single organic solvent was our original finding compare with previous conventional organic solvent. The reaction rate was elevated by the added amount of 1-butanol. The enhanced reaction rate was about 150-folds. This enhancement was speculated as 1-butanol adsorption on the microinterface. The adsorbed 1-butanol improved the properties of microinterface, especially its mobility was increased by difference of the chain length between phosphatidylcholine and 1-butanol. PhospholipaseA$_2$ molecules were located on the microinterface due to modified mobility of microinterface. Located phospholipaseA$_2$ on the microinterface reacted easily with phosphatidylcholine molecule. As a result high reaction rate was obtained. Microinterfacial properties were successfully improved by adsorbed 1-butanol molecule, and were favorable to appear higher reactivity of phospholipaseA$_2$.

• 한국염색가공학회지
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• 제6권1호
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• pp.33-43
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• 1994

In the present work, to clarify the mechanism of the neutral salt effect on the alkaline hydrolysis of PET, many salts with different cations like LiCl, NaCl, KCl, CsCl were added to the aqueous alkaline solutions. Then PET was hydrolyzed with aqueous solutions of many salts in alkali metal hydroxides under various conditions. Some conclusions obtained from the experimental results were summarized as follows. The reaction rate of the alkaline hydrolysis of PET was increased by the addition of neutral salts and In k was increased nearly linearly with the square root of ionic strength of reaction medium. This fact suggested that the ionic strength effect by Debye-Huckel and Bronsted theory was exerted on the reaction. The specific salt effect was also observed. The reaction rate was increased with the increase in the electrophilicity of cations of neutral salts, i. e., in the order of $Cs^+$/ < $K^+$/ $a^+$/ $i^$^+$. It was considered that the reaction rate was increased in the order of C $s^+$. < $K^+$. $a^+$. $i^+$. because the lowering effect of the cations on the negative charge of PET surface was increased with the electrophilicity of cations. It was thought that $E_{a}$ was increased because the cations of neutral salts decreased the negative charge of PET surface. It, however, was inferred from the increase in ${\Delta}$S＊ and the decrease in the ${\Delta}$G＊ that the cations of neutral salts associated with PET increased the collision frequency between carbonyl carbon and OH- ion and then accelerated the reaction rate.te.

• Biotechnology and Bioprocess Engineering:BBE
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• 제9권1호
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• pp.62-64
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• 2004

The use of enantioselective hydrolysis for preparing chiral epichlorohydrins was investigated using recombinant Pichia pastoris with the enantioselective epoxide hydrolase of Rhodotorula glutinis. The rate of the recombinant epoxide hydrolase-catalyzed enantioselective hydrolysis of racemic epichlorohydrins was enhanced by the addition of 5%(v/v) Tween 20. Enantiopure (R)-epichlorohydrins with an enantiopurity of 100% ee and a yield of 26% were obtained within 5min from 50mM racemates.

• Journal of Pharmaceutical Investigation
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• 제14권3호
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• pp.131-135
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• 1984

염산디싸이클로민은 항(抗)콜린성(性) 약물로 소화성궤양(消化性潰瘍) 치료제로서 제산제(制酸劑)와 함께 널리 사용되고 있다. 전보(前報) 에서 이 약물의 수용액(水溶液)에서의 가수분해반응기구연구(加水分解反應機構硏究)를 통하여 반응차수(反應次數) 및 속도(速度) 등을 보고(報告)한 바 있으며 본(本) 연구(硏究)에서는 수용액(水溶液)에서의 가수분해(加水分解)에 미치는 pH의 영향을 검토하였고 또한 제산제성분(制酸劑成分)인 magnesium ion이 가수분해(加水分解)에 미치는 영향 등을 검토하였다.

• Biotechnology and Bioprocess Engineering:BBE
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• 제7권6호
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• pp.367-370
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• 2002

Candida cylindracea lipase was immobilized by adsorption on acid washed glass beads. It was observed that protein loading of the support depends on the size of the particle, with smaller particle containing higher amount of protein per unit weight. Initial reaction rate linearly varied up to enzyme concentration of 17.25 U/mL. Amount of free fatty acids produced was linearly proportional up to the enzyme loading of 1650 $\mu$g/g of bead. Achievement of chemical equilibrium took longer time in the case of less protein loading. Degree of hydrolysis was found to decrease in second and third consecutive batch operations on repeated use of immobilized lipase.

• KSBB Journal
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• 제4권3호
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• pp.235-240
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• 1989

본 연구에서는 매년 700여만톤 생산되는 볏짚을 자원화 하기 위하여 암모니아-냉동-파열법 (AFEX)을 사용하였다. AFEX으로 전처리된 볏짚은 처리되지 않은 것보다 대랴 4배 이상의 가수분해율을 얻을 수 있었다. 또한 어떼한 전처리 방법보다도 처리하는 과정이 쉽고 당화율도 90%로 이상이며, 경제성이 높다.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.336.1-336.1
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• 2002

HSP100/Clp family functions as molecular chaperone and ATP dependent protease. The Streptococcus pneumoniae ClpL. a homologue of bacterial ClpB and yeast cytosolic HSP 104. is one of major heat shock proteins but its biochemical properties are unknown. In this study. ClpL in Streptococcus pneumoniaewas characterized using histidine tagged recombinant ClpL. When ATP hydrolysis activity was compared in the presence or absence of a variety of nucleotides or divalent ions. either ATP or Mn$2^＋$ ion was found to increase significantly the rate of ATP hydrolysis. Furthermore. glutaraldehyde cross-linking and subsequent native-PAGE analfysis showed that ClpL forms dimer. but in the presence of 4 mM concentration of $Mn^{2＋}$ion as a cofactor for ATP hydrolysis and oligormerization in vitro.

• Journal of the Korean Wood Science and Technology
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• 제37권6호
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• pp.578-584
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• 2009

백합나무 목분으로 고농도 단당류를 생산하기 위하여 진한 황산을 사용하는 산 가수분해 특성을 연구하였다. 목분과 황산의 비율을 달리하거나 2차 가수분해의 온도와 시간을 달리하여 당화액 제조의 최적 조건을 탐구한 결과, 1차 가수분해의 목분과 72% 황산 비율은 1 : 2.61(w/w)였으며, 2차 가수분해 온도와 시간은 $105^{\circ}C$에서 70분 가수분해 조건이었다. 이때 생성된 당화액의 농도는 glucose가 44.8 g/L였고 xylose는 25.2 g/L였다. 산 가수분해를 통하여 얻어진 당화액을 발효할 때 발효 저해물질로 알려진 furfural, 5-HMF (5-hydroxymethylfurfural), 저분자량 페놀성 화합물들이 생성되었는데 furfural과 5-HMF는 2차 가수분해 온도가 높아짐에 따라, 그리고 반응시간이 길어짐에 따라 생성량이 증가하였다. $110^{\circ}C$ 2차 가수분해 조건에서 반응시간이 40분을 지남에 따라서 xylose농도는 감소하였고 glucose 농도는 일정하였는데, xylose는 생성속도보다 furfural로 전이 속도가 더 빠른 것으로 생각되고, glucose의 경우 생성속도와 5-HMF로 전이속도가 비슷하여 농도가 일정하게 나타났다.