• 제목/요약/키워드: Selectivity coefficient

검색결과 101건 처리시간 0.024초

Seasonal Variation in Catchability of Penaeid Prawns in the Night-time Prawn Fishery in Albatross Bay, Gulf of Carpentaria, Australia

  • Park Young Cheol;Warburton Kevin;Die David J.
    • Fisheries and Aquatic Sciences
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    • 제5권2호
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    • pp.114-121
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    • 2002
  • A correction index of catchability (CIC) was derived using a 6 year research data set to examine the seasonal variation in catchability for the night time prawn fishery in Albatross Bay. CIC reflects the composite effect of the monthly variation in size selectivity, emergence­burying behaviour and population density variation of prawn populations. The values of CIC for four dominant species, Metapenaeus endeavouri, M. ensis, Penaeus semisulcatus and P. esculentus, were examined. The value of CIC for M. endeavouri varied substantially and was the highest in August. The values of CIC for M. ensis were high during November to March and the seasonality was weaker than that for M. endeavouri. The monthly variation in CIC for P. semisulcatus reflected the seasonal variation in population density, being high during November to February. These results suggest that the catch ability of P. esculentus is steady throughout the year but it varies greatly on a seasonal basis for M. endeavouri.

Extractive Recovery of Products from Fermentation Broths

  • Kim, Joong-Kyun;Eugene L. Iannotti;Rakesh Bajpai
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제4권1호
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    • pp.1-11
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    • 1999
  • Considerations of partition coefficients, selectivity, biocompatibility, and waste generation are important in selection of appropriate solvents to be used for extractive recovery of products from fermentation broths. Several selection criteria can be used based upon the nature of different species present in the broth. These criteria, along with examples of specific case studies, were presented. These serve not only in screening of useful solvents, but also in pointing to the specific modes of operation of recovery-coupled bioprocesses.

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이온교환법에 의한 탈질소 공정개발의 기초연구(V) -질산성 질소 선택적인 이온교환수지의 합성- (Basic Study for Development of Denitrogenation Process by Ion Exchange(V) -Synthesis of Nitrate-Selective Ion Exchange Resines-)

  • 이동환;김승일;전진희;박찬영;이민규
    • 한국환경과학회지
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    • 제9권4호
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    • pp.319-323
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    • 2000
  • Nitrate-selective ion exchange resin which have bulky tertiary amine as functional group have been synthesized by the reaction of chloromethylated polystyrene-divinylbenzene copolymer and the corresponding tertiary amine [$NR_3=NE_{t3} 1, N{(C_2 H_4 H_3)}_32]$in ethanol, while commercial resin has $NMe_3$ as functional group. The fundamental properties such as bulk density, water content, appearance index, exchange capacity, effective size, uniformity coefficient of synthesized anion exchange resin (1) have been measured. The ion exchange resin (1) and (2) exhibited the better selectivity for nitrate than sulfate in both batch and continuous column experiments.

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Pilymeric Membrane Sodium Ion-Selective Electrodes Based on Calix[4}arene Triesters

  • 김윤덕;정해상;강성옥;남계천;전승원
    • Bulletin of the Korean Chemical Society
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    • 제22권4호
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    • pp.405-408
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    • 2001
  • New lipophilic triesters of calix[4]arene and calix[4]quinone are investigated as sodium ion-selective ionophores in poly(vinyl chloride) membrane electrodes. For an ion selective electrode based on calix[4]arene triester I, the linear response is 1 ${\times}$10-3.5 to 1 ${\times}$ 10-1 M of Na+ concentrations. The selectivity coefficients for sodium ion over alkali metal and ammonium ions are determined. The detection limit (logaNa+ = -4.50) and the selectivity coefficient (logKNa+,K+pot = -1.86) are obtained for polymeric membrane electrode containing calix[4]arene triester I.

A Mechanistic Study on Acyl Transfer Reactions of Aryl Substituted Benzoates Between Aryloxides

  • Ik-Hwan Um;Jae-Shin Jeon;Dong-Sook Kwon
    • Bulletin of the Korean Chemical Society
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    • 제12권4호
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    • pp.406-410
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    • 1991
  • Second order rate constants have been measured spectrophotometrically for reactions of 4-nitrophenyl substituted benzoates with various aryloxides and aryl benzoates with p-chlorophenoxide. The reactivity has exhibited significant dependences on the electronic nature of the substituent in the acyl moiety of the substrate and in the nucleophilic phenoxide, while the substituent in the leaving phenoxide has little influenced the reactivity. The Bronsted coefficient $\beta$ values so obtiained support that the present acyl transfer reaction proceeds via a stepwise mechanism in which the nucleophilic attack would be the rate-determining step. Interestingly, the magnitude of the $\betaacyl$ and $\beta$ nuc increases with increasing reactivity, implying that the reactivity selectivity principle is not operative in the present system. The failure of the reactivity selectivity principle is attributed to a change in transition state structure upon the substituent variation in the present acyl transfer reaction.

Polymeric Membrane Cesium-Selective Electrodes Based on Quadruply-bridged Calix[6]arenes

  • 최은미;오혜진;고승화;최용국;남계춘;전승원
    • Bulletin of the Korean Chemical Society
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    • 제22권12호
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    • pp.1345-1349
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    • 2001
  • New quadruply-bridged calix[6]arenes (I-V) have been studied as cesium selective ionophores in poly(vinyl chloride) (PVC) membrane electrodes. PVC membranes were prepared with dioctyl sebacate (DOS) or 2-nitrophenyl octyl ether (o-NPOE) as the sol vent mediator and potassium tetrakis(p-chlorophenyl)borate as the lipophilic salt additive. These ionophores produced electrodes with near-Nernstian slope. The selectivity coefficients for cesium ion with respect to alkali, alkaline earth and ammonium ions have been determined. The lowest detection limit (logaCs+ = -6.3) and the higher selectivity coefficient (logkpotCs+,Rb+ = -2.1 by SSM, -2.3 by FIM for calix[6]arene I) for Cs+ have been obtained for membranes containing quadruply-bridged calix[6]arenes (I, Ⅱ, Ⅲ), which have no para t-butyl substituents on the bridging benzene ring.

모델 콜타르 유분 중에 함유된 질소고리화합물의 추출에 관한 메탄올과 포름아마이드의 비교 (Comparison of Methanol with Formamide on Extraction of Nitrogen Heterocyclic Compounds Contained in Model Coal Tar Fraction)

  • 김수진
    • 공업화학
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    • 제26권2호
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    • pp.234-238
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    • 2015
  • 모델 콜타르 유분 중에 함유된 질소고리화합물(NHC)의 분리를 메탄올과 포름아마이드 추출에 의해 비교했다. 원료로서는 4종류의 NHC (NHCs : 퀴놀린, 이소퀴놀린, 인돌, 퀴날딘), 3종류의 2환 방향족 화합물(BACs : 1-메틸나프탈렌, 2-메틸나프탈렌, 디메틸나프탈렌), 비페닐과 페닐에테르로 제조한 모델 콜타르 유분을 사용했다. 용매로서는 메탄올과 포름아마이드 수용액을 사용했다. 원료와 용매의 접촉 장치로서는 회분 교반기를 사용했다. 사용한 용매와 무관하게, 초기 용매 함수율의 감소와 평형조작 온도의 상승은 NHCs의 분배계수를 급격히 증가시켰으나, 역으로 BACs를 기준한 NHCs의 선택도를 감소시켰다. 초기 용매/원료의 체적비가 감소함에 따라 NHCs의 분배계수는 감소했으나, BACs를 기준한 NHCs의 선택도는 거의 일정했다. 동일한 실험조건에서, NHCs의 분배계수는 메탄올 추출이 포름아마이드 추출에 비해 약 3~5배 높았으나, BACs를 기준한 NHCs의 선택도는 역으로 포름아마이드 추출이 메탄올 추출에 비해 3~7배 높았다. 또한, NHCs의 용해력과 선택도의 밸런스에 NHCs의 추출처리속도를 부가하여 두 용매 추출법을 비교했다.

용매 추출에 의한 조제 메틸나프탈렌유에 함유된 함 질소화합물의 저감에 관한 실험적 연구(I): 5성분계 모델 조제 메틸나프탈렌유에 함유된 함 질소화합물의 저감 (Experimental Study on Reduction of Nitrogen-Containing Compounds Contained in Crude Methylnaphthalene Oil by Solvent Extraction (I): Reduction of Nitrogen-Containing Compounds Contained in Model Crude Methylnaphthalene Oil of 5 Components System)

  • 강호철;김수진
    • 공업화학
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    • 제33권4호
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    • pp.431-435
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    • 2022
  • 용매 추출에 의해 5성분계 모델 조제 메틸나프탈렌유(CMNO)에 함유된 함 질소화합물(NC)의 저감을 실험적으로 검토했다. 원료로서는 3종류의 NC [퀴놀린(QU), 이소퀴놀린(IQU), 인돌(IN)]과 2종류의 2환 방향족화합물[1-메틸나프탈렌(1MNA), 2-메틸나프탈렌(2MNA)]로 구성된 5성분계 모델 CMNO를, 용매로서는 포름아미드 수용액을 각각 사용했다. 초기 용매에 함유된 물의 체적분율(yw,0)의 증가는 NC의 분배계수와 수율을 급격히 감소시켰으나, 역으로 2MNA을 기준한 NC의 선택도를 증가시켰으며 용매/원료의 체적분율(S/F)의 증가는 NC의 분배계수, 수율과 선택도를 동시에 증가시켰다. 일정한 조건(yw,0 = 0.1, S/F = 1, 평형온도 303 K)하에서 얻어진 QU, IQU과 IN의 수율은 30%, 31%와 40%를, 선택도는 15, 15, 20을 각각 보였다. 우수한 NC의 수율과 선택도로부터 본 연구의 포름아미드 추출법은 모델 CMNO에 함유된 NC의 저감법으로 기대되었다.

Selectivity of Oxomemazine for the $M_1$ Muscarinic Receptors

  • Lee, Shin-Woong;Woo, Chang-Woo;Kim, Jeung-Gu
    • Archives of Pharmacal Research
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    • 제17권6호
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    • pp.443-451
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    • 1994
  • The binding characteristics of pirenzepine and oxomemazine to muscarinic receptor were studied to evaluate the selectivity of oxomemazine for the muscarinic receptor subtypes in rat cerebral microsomes. Equililbrium dissociation constant $(K_D){\;}of{\;}(-)[^3H]$quinuclidinyl benzilate$([^3H)QNB)$ determined from saturation isotherms was 64-pM. Analysis of the pirenzepine inghibition curve of [$^3H$]QNB binding to cerebral microsome indicatd the presence of two receptor subtypes with high $(K_1 = 16 nM, M_1 receptor)$two receptor subypes with about 20-fold difference in the affinity for high $(k_1 = 84nM, {\;} O_H receptor){\;} and {\;}low{\;} (K_1{\;} ={\;} 1.65\muM, {\;} O_L receptor$) affinity sites. The percentage populations of $M_1{\;} and M_3$, /TEX> receptors to the total receptors were 61 : 39, and those of $O_H{\;} and{\;} O_L$ receptors 39 : 61, resepectively. Both pirenzepine and oxomemazine increaed the $K_D$ value for $[^3H]QNB$ without affecting the binding site concentrations and Hii coefficient for the $[^3H]QNB$ without affecting the binding site concentractions and Hill coefficient for the [$^{3}$H]QNB binding. Oxomemazine had a 10-fold higher affinity at $M_1$ receptors than at $M_3$ receptors, and pirenzepine a 8-fold higher affinity at $O_H$ receptors were of $O_H$ receptors and 71% of $M_3$ receptors. However, $M_3$for oxomemazine and $O_H$for pirenzepine were composed of a uniform population. These results suggest that oxomemazine could be classified as a selective drug for $M_1$ receptors and also demonstrate that rat cerebral microsomes contain three different subtypes of $M_1{\;} M_3$ and the other site which is different from $M_1, {\;} M_2$, /TEX> receptors.

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${\beta}-Ag_3SI$ 단결정막 전극에 관한 연구 (${\beta}-Ag_3SI$ Single Crystal Membrane Electrode)

  • 신두순;이선천
    • 대한화학회지
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    • 제28권2호
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    • pp.86-94
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    • 1984
  • ${\beta}-Ag_3SI$의 단결정을 만들어 막전극으로의 응용을 살펴보았다. 그 결과 할로겐 이온들에 대해 감응함을 알았고, 분리용액법과 혼합용액법으로 할로겐 이온들에 대한 선택계수를 얻어 이론값과 비교검토 하였으며, 전위시간 곡선으로 부터 이 전극이 유리 전극기구에 의해 전도함을 알았고, 넓은 pH 범위에서 전위가 일정한 값을 가짐을 알았다. 한편 분석화학에의 응용을 살펴 본 결과 할로겐이온의 혼합용액에서 좋은 지시전극으로 사용할 수 있음을 알았다

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