• 멤브레인
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• 제30권2호
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• pp.111-123
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• 2020

산업화와 기후 변화는 깨끗한 식수에 대한 수요 증가를 초래하였다. 막분리공정을 이용한 해수담수화는 물의 수요에 대한 요구를 채울 수 있는 경제적으로 실현 가능한 대안 중 하나이다. 막분리공정에서 2차원 재료들은 기존 역삼투분리막(reverse osmosis membrane) 기반의 폴리아마이드 박막복합막(TFC-PA)과 비교하였을 때 막의 강도를 높여주고 투수성을 용이하게 하며 높은 염제거율 및 높은 선속률과 선택성을 보여준다. 이 리뷰 논문에서는 재료, 합성, 특징, 해수담수화 과정을 기반으로 다양한 2차원 재료로 구성된 복합막들을 소개하고 있다.

• 멤브레인
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• 제8권1호
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• pp.29-41
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• 1998

수용상 MPD(m-phenylene diamine)와 유기상 TMC(trimesoyl chloride)를 사용하여 역삼투 복합막의 활성층 고분자인 aromatic polyamide 제조를 행하고 그 성능을 고찰하였다. 또한 polysulfone 다공성 지지막 위에 박막을 회분, 연속식으로 계면중합 제조한 후, 제조변수에 따른 역삼투 성능을 비교하였다. 회분식으로 복합막을 제조한 결과 유기상 용매의 종류, 단량체의 농도와 함침시간, 열처리 온도, 중화제, 알코올 후처리, 산 후처리 등에 의해 다양한 성능을 나타내었다. 이때, 투과량 향상에는 알코올 후처리 효과가, 또 선택도의 향상에는 단량체의 농도와 함침시간이 변수이었다. 최적조건에서 연속식 공정으로 막모듈을 제조하여 NaCl 5,000 ppm, $25kg_f/cm^2$에서 상용막과 비교할때, 투과량은 33% 증가하고 배제율은 5% 감소하였다.

• 환경위생공학
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• 제16권3호
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• pp.72-79
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• 2001

The selective catalytic oxidation of toxic aromatic solvents (benzene, toluene, ethylbenzene, and styrene) and their mixtures were studied on a $Pt/{\;}{\gamma}-Al_2O_3$ catalyst at temperature ranging from $160~350^{\circ}C$. The deep conversion of aromatic solvents was increased as the inlet concentration was decreased and the reaction temperature was increased. The reactivity increases in order benzene > toluene > ethylbenzene > styrene. In mixture, remarkable effects on reaction rate and selectivity have been evidence ; the strongest inhibition effect is shown by styrene and increase in a reverse order with respect to that of reactivity. The inhibition effect was increased in order styrene > ethylbenzene > toluzene > benzene. This trend is due to the competition adsorption between the two or three reactants on the oxidized catalyst. Also, the deep conversion change of benzene was a small in tertiary mixtures(including of benzene and styrene) comparing with conversion characteristics of binary mixture with styrene. This result was due to small concentration of styrene. which had very strong inhibition effect.

• 한국동물학회:학술대회논문집
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• 한국동물학회 2003년도 한국생물과학협회 학술발표대회
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• pp.161.2-161
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• 2003

No Abstract, See Full Text

• Biomolecules & Therapeutics
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• 제16권2호
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• pp.168-172
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• 2008

The present study is to determine of sensitive nicorandil analysis method using HPLC and measure the pharmacokinetics parameters (bioavailability, $C_{max}$, $T_{max}$, Ke, $T_{1/2}$) of nicorandil (5 mg, Tab; Choongwae Pharma Corporation). Plasma (500 ul) was mixed with furosemide (internal standard, 500 ug/ml). Detection wavelength was 256 nm. The mixture of 0.01 M ammonium acetate and acetonitrile 80:20 (v/v) was used mobile phase. The HPLC separation was accomplished on ODC reverse HPLC column. The nicorandil was analyzed by a HPLC system, which consists of CAPCELL PAK C18 column (5 ${\mu}$m, 4.6 × 150 mm) and a chromatography data analysis S/W, using a isocratic mobile phase (mixture of 0.01 M ammonium acetate and acetonitrile 80:20 ) at 1.0 ml/min. Its sensitivity, selectivity, accuracy and precision must be adequate for the bioavailabilty study of nicorandil, and the linearity ($r^2$ ≥ 0.9994) of nicorandil was also proved in the range of 0.05 ug/ml . 3 ug/ml. The pharmacokinetic parameters of nicorandil (5 mg) tablets were measured as the follow. AUC: 0.19 ug/ml·hr, $C_{max}$: 0.14 ug/ml, $t_{max}$: 0.58 hr, Ke: 0.11 hr., $t_{1/2\beta}$: 6.76 hrs. This method is simple and sensitive HPLC method using UV detector for determination of nicorandil in human plasma.

• 멤브레인
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• 제1권1호
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• pp.5-12
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• 1991

Since the discovery of the Loeb-Sourirajan reverse osmosis membrane, thirty years have passed and many membrane technologies and new membranes for applications have been developed in the world. In the early stage of these developments Japan has not contributed much, but from the middle of 70ties Japan has started its own R&D projects starting from the desalination technology, and now various private industries and government ministries are actively engaging in R & D of membrane technologies in Japan. In Table 1 the chronological developments of important events of developments and projects relating membrane technologies inside and outside of Japan are introduced and their details will be explained. The first membrane technology applied in the Japanese industry was a electrodialysis(ED) process using ion-exchange membranes. These membranes were first developed in early 50ties and the Japanese government decided to use this method for concentration of sea-water to produce salt, which was then produced by solar evaporation. This development program started from 1960 by the Japan Monopoly Corp.(at that time). To apply ED process for sea-water concentration it was necessary to develop ion-exchange membranes having very low electric resistance to avoid energy loss due to Joule heat, and those having selectivity to permeate single valent ions only to avoid scale formation in the ED stacks. Three Japanese companies, Asahi Glass, Asahi Chemical and Tokuyama Soda, have succeeded to develop such membranes, and until 1971 all of the seven salt manufacturing companies had adopted ED for production of food salt.

• 한국수소및신에너지학회논문집
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• 제13권3호
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• pp.214-223
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• 2002

Kinetic and effectiveness factors for methanol steam reforming using commercial copper-containing catalysts in a plug flow reactor were investigated over the temperature ranges of $180-250^{\circ}C$ at atmospheric pressure. The selectivity of $CO_2$/$H_2$ was almost 100%, and CO products were not observed under reaction conditions employed in this work. It was indicated that $CO_2$ was directly produced and CO was formed via the reverse water gas shift reaction after methanol steam reforming. The intrinsic kinetics for such reactions were well described by the Langmuir-Hinshelwood model based on the dual-site mechanism. The six parameters in this model, including the activation energy of 103kJ/mol, were estimated from diffusion-free data. The significant effect of internal diffusion was observed for temperature higher than $230^{\circ}C$ or particle sizes larger than 0.36mm. In the diflusion-limited case, this model combined with internal effectiveness factors was also found to be good agreement with experimental data.

• Archives of Pharmacal Research
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• 제25권5호
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• pp.647-651
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• 2002

An LC/MS/MS method for the simultaneous determination of a neuroprotective agent for ischemia-reperfusion damage, KR-31378 and its N-acetyl metabolite KR-31612 in human plasma was developed. KR-31378, KR-31612 and the internal standard. KR-31543 were extracted from human plasma by liquid-liquid extraction. A reverse-phase HPLC separation was performed on Luna phenylhexyl column with the mixture of acetonitrile-5 mM ammonium formate (55:45, v/v) as mobile phase. The detection of analytes was performed using an electrospray ionization tandem mass spectrometry in the multiple reaction monitoring mode. The lower limits of quantification for KR-31378 and KR-31612 were 2.0 ng/ml. The method showed a satisfactory sensitivity, precision, accuracy, recovery and selectivity.

• Journal of Microbiology and Biotechnology
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• 제22권3호
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• pp.431-435
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• 2012

In this study, we describe a novel approach to achieve replicative selectivity of conditionally replicative adenovirus that is based upon trans-splicing ribozyme-mediated replacement of cancer-specific RNAs. We developed a specific ribozyme that can reprogram human telomerase reverse transcriptase (hTERT) RNA to induce adenoviral E1A gene expression selectively in cancer cells that express the RNA. Western blot analysis showed that the ribozyme highly selectively triggered E1A expression in hTERT-expressing cancer cells. RT-PCR and sequencing analysis indicated that the ribozyme-mediated E1A induction was caused via a high fidelity trans-splicing reaction with the targeted residue in the hTERT-expressing cells. Moreover, reporter activity under the control of an E1A-dependent E3 promoter was highly transactivated in hTERT-expressing cancer cells. Therefore, adenovirus containing the hTERT RNA-targeting trans-splicing ribozyme would be a promising anticancer agent through selective replication in cancer cells and thus specific destruction of the infected cells.

• 분석과학
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• 제10권1호
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• pp.9-17
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• 1997

nitrophenol류는 미국 환경청에서 주요 priority 오염물질로 규정하고 있다. 물 중에 존재하는 nitrophenol류의 혼합물을 분석하기 위해 역상 액체크로마토그래피법에 대기압 화학이온화법을 연결한 질량분석기를 이용하였다. 추가적으로, 선택이온 검색법과 cone 전압차분해법(cone voltage fragmentation)을 이용하여 nitrophenol류의 확인에 있어서 감도와 선택성을 높였다. nitrophenol의 분해 형태는 충돌유발분해법인 MS/MS 기법으로 얻어진 분해 형태와 비교하였다.