• Title/Summary/Keyword: solutes

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Thermodynamic Properties of the Solute Transfer from the Aqueous Acetonitrile Mobile Phase to the Stationary Phase Monitored by HPLC

  • 정원조;김지연;구윤모
    • Bulletin of the Korean Chemical Society
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    • 제21권1호
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    • pp.105-109
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    • 2000
  • High-performance liquid chromatography is suitable for getting thermodynamic information about solute-solvent interactions. We used a squalane impregnated $C_{18}$ phase as a presumably bulk-like stationary phase to secure a simple partition mechanism for solute retention in reversed phase liquid chromatographic system. We measured retention data of some selected solutes (benzene, toluene, ethylbenzene, propylbenzene, butylbenzene, phenol, benzylalcohol, phenethylalcohol, benzylacetone, acetophenone, benzonitrile, benzylcyanide) at 25, 30, 35, 40, 45, and 50 $^{\circ}C$ in 30/70, 40/60, 50/50, 60/40 and 70/30 (v/v%) acetonitrile/water eluents. The van't Hoff plots were nicely linear, thus we calculated dependable thermodynamic values such as enthalpies and entropies of solute transfer from the mobile phase to the stationary phase based on more than four retention measurements on different days (or weeks). We found that the cavity formation effect was the major factor in solute distribution between the mobile and stationary phases in the system studied here. Our data were com-pared with some relevant literature data.

A Modified Adsorption Model for Retention of Nonpolar Solutes in Reversed Phase Liquid Chromatography

  • Cheong Won Jo
    • Bulletin of the Korean Chemical Society
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    • 제15권1호
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    • pp.15-20
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    • 1994
  • The adsorption model in reversed phase liquid chromatography has been critically examined. It has been found that use of the Everett type surface activity coefficient for the solute in the stationary phase is not useful to study the retention characteristics of a nonpolar solute. We suggest a modified model. In this model it is assumed that the displaced modifier molecules from the surface monolayer do not transfer into the bulk mobile phase but stick to the nonpolar solute which has displaced them. In addition, we prefer to use an apparent stationary phase activity coefficient of the soluie instead of the Everett type activity coefficient. This modified adsorption model well explains the mobile and stationary phase effects on the solute retention upon variation of mobile phase composition.

New Device for Addition of Modifier to Supercritical Fluid Carbon Dioxide Mobile Phase

  • 표동진;김호현
    • Bulletin of the Korean Chemical Society
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    • 제18권6호
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    • pp.584-588
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    • 1997
  • A new device to accurately deliver small amount of modifier into supercritical carbon dioxide fluid is described. Carbon dioxide, the most widely used mobile phase in supercritical fluid chromatography, is a relatively non-polar fluid, and hence the addition of small amount of polar modifiers could be necessary to migrate polar solutes. In this work, supercritical CO₂and modifier are delivered from the pump to a 100 μL mixing chamber in which a small magnetic bar is rotating. After passing through the mixing chamber, supercritical CO₂is changed to a new mobile phase with different polarity. The amount of modifier added into supercritical CO₂is measured by an amperometric microsensor, which is prepared from a thin film of perfluorosulfonate ionomer.

Preferential Solvation and Statistical Analysis for Solvent Polarity Parameters in MeOH Binary Mixtures

  • Sakong Yeol;Yoo Seoung-Kyo;Lee Ikchoon
    • Bulletin of the Korean Chemical Society
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    • 제13권6호
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    • pp.636-642
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    • 1992
  • Preferential solvation (PS) phenomena of solutes based on solvent polarity, $E_T$ and AN, were studied by UV/vis. and NMR spectra in MeOH binary mixtures. According to the extent of solvent-solvent interaction, different solvation phenomena were found. PS concept was applied to explain the reactivity of tert-butyl halides solvolysis. The findings of solvation phenomena have been related to the rate of solvolysis and PS suggested as a reason for the solvent dependence of the rates of reaction. Moreover, we found that the results of principal components analysis using six parameters are in good accordance with the results of PS phenomena in mixed methanol systems.

Dual Capillary Column System for the Qualitative Gas Chromatography: 2. Comparison between Splitless and On-Column Injection Modes

  • Kim, Kyoung-Rae;Kim, Jung-Han;Park, Hyoung-Kook;Oh, Chang-Hwan
    • Bulletin of the Korean Chemical Society
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    • 제14권2호
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    • pp.250-255
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    • 1993
  • A dual capillary column system is described for the simultaneous analysis of a given sample and measurement of retention index (RI) and area ratio (AR) values of each peak on two capillary columns of different polarity, DB-5 & DB-1701 from a single injection. Both capillary columns were connected to either a splitless injector or an on-column injector via a deactivated fused-silica capillary tubing of 1 m length and a 'Y' splitter. Both injection modes allowed to measure RI and AR values with high reproducibility (<0.01% RSD) and high accuracy (<10% RE), respectively with the exception that the trace and high boiling solutes required the on-column mode for the accurate quantification and AR comparison. When the dual capillary column system in on-column injection mode was applied to the blind samples containing organic acids, each acid was positively indentified by the combined computer RI library search-AR comparison.

Modulation of electroosmosis using penetration enhancers

  • Kim, Su-Youn;Lee, Yeon-Joo;Lee, Hyung-Won;Lee, Hyo-Jung;Lee, Seung-Yeon;Youe, Jee-Sun;Oh, Seaung-Youl
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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    • pp.293.1-293.1
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    • 2003
  • Electroosmotic flux during iontophoresis originates due to the net negative charge of the current passing channels (pores) in skin at physiological pH (pH 7.4). Thus, the channels are permselective to cations, and this causes the convective solvent flow from anode to cathodal direction. This solvent flow facilitates the flux of cations (from anode), inhibits that of anions (from cathode), and enables theenhanced transport of neutral, polar solutes. (omitted)

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Effect of Polyethlene Glycols on the Electroosmosis Through Skin

  • Lee, Seung-Yeon;Kim, Su-Youn;Youe, Jee-Sun;Min, Hye-Ran;Han, Jeong-Jin;Oh, Seaung-Youl
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.233.3-234
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    • 2003
  • Electroosmotic flux during iontophoresis originates due to the net negative charge of the current passing channel (pores) in skin at physiological pH (pH 7.4). Thus, the channel is permselective to cations, and this causes the convective solvent flow, from anode to cathode direction. This solvent flow facilitates the flux of cations (from anode), inhibits that of anions (from cathode), and enables the enhanced transport of neutral, polar solutes. In this work, we have investigated the effect of a series of polyethylene glycols (PEGs) with different molecular weights on the electroosmtic flow to get more detail understanding of this phenomena. (omitted)

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시효한 Mg-5%Sn 합금의 경도와 진동감쇠능 변화 (Changes in Hardness and Damping Capacity of Aged Mg-5%Sn Alloy)

  • 전중환
    • 열처리공학회지
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    • 제35권5호
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    • pp.255-261
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    • 2022
  • In this work, the strain-amplitude independent and strain-amplitude dependent damping capacities of Mg-5%Sn alloy have been investigated as a function of its age-hardening response. The hardness increased with an increase in aging time, reached a peak value after 48 h, and then it gradually decreased. The damping capacities of the Mg-5%Sn alloy exhibited a decreasing tendency in the order of solution-treated, under-aged, peakaged, and over-aged states in the strain-amplitude dependent region, whereas they increased continuously with aging time in the strain-amplitude independent region. The microstructural examination during aging revealed that the lower concentration of Sn solutes in the α-(Mg) matrix and the lower density of the Mg2Sn precipitate particles may well be the crucial factors for better damping values in the strain-amplitude independent and strain-amplitude dependent regions, respectively.

수처리용 세라믹 기반 그래핀 맴브레인의 합성 및 물질이동특성 (Fabrication of Ceramic-based Graphene Membrane (CbGM) and Its Mass Transport Behavior for Water Treatment)

  • 김창민;박기범;김광수;김인수
    • 대한환경공학회지
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    • 제37권11호
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    • pp.649-655
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    • 2015
  • 본 연구에서는 막 기반 수처리 기술의 핵심인 막 성능 및 특성을 혁신적으로 개선시키기 위한 새로운 형태의 막으로서 그래핀과 세라믹을 결합하는 세라믹 기반 그래핀 막(Ceramic-based graphene membrane (CbGM))을 만들고, 막에서 일어나는 물질 이동 특성을 파악하였다. 수투과 및 염 제거의 역할을 하는 활성층으로서 그래핀이 사용되었으며, 간단한 Filtration-assisted assembly (FAA) 방법을 도입하여 막을 합성하였다. 합성한 막의 표면 형태 및 특성 분석을 위해 주사전자 현미경 및 접촉각을 분석하였으며, 막 성능 및 특성 파악을 위해 3가지 용질(i.e., NaCl, $MgCl_2$, $Na_2SO_4$)을 회분식 정삼투 시스템에서 용질 이동을 측정하였다. 표면 형태 특성 분석과 물질 이동 결과를 통해, 그래핀 층의 두께 보다는, 활성층을 구성하는 그래핀 조각들 사이의 교합(Interlocking)이 막에 선택성 부여함에 있어서 가장 중요함을 확인하였다. 또한, 농도차를 구동력으로 하는 막 공정에 CbGM을 적용하였을 때, 수중의 음이온과 양이온의 최외각 전하비($Z^-/Z^+$)값이 증가할수록 용질 이동이 비례적으로 촉진되었으므로, CbGM의 표면이 양으로 하전되어 있으며, 이것이 전하된 물질의 이동에 매우 큰 영향을 끼친다는 것을 확인하였다.

개에서 복막투석 적용: 20 증례 (2006-2008) (Peritoneal Dialysis in Dogs: 20 cases (2006-2008))

  • 남소정;최란;오원석;현창백
    • 한국임상수의학회지
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    • 제26권1호
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    • pp.23-28
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    • 2009
  • 복막투석은 정상적인 생리적 상태의 장애를 야기하는 체내의 독성물질을 치료적으로 제거하는 임상적 방법이다. 본 연구에서는 신부전으로 내원한 환자에게 복막투석을 적용한 20증례의 임상적 결과와 합병증을 후향적으로 평가하였다. 복막투석을 실시하는 동안 적혈구수, 혈구용적, 신기능과 관련된 혈액 화학적 수치 및 전해질 등의 혈액학적 분석과 합병증, 임상적 결과 등을 기록하였다. 복막투석의 결과로 19마리의 개에서 혈중 요소 질산 농도가 유의하게 감소하였고 (p<0.05), 17마리의 개에서 혈중 크레아티닌의 농도가 유의하게 감소하였다 (p<0.05). 복막투석의 부작용으로는 저알부민혈증(12/20, 60%), 빈혈(10/20, 50%), 투석액의 피하 누출(9/20, 45%), 세균성 복막염 (6/20, 30%), 투석액의 저류 (5/20, 25%)와 사지의 부종(4/20, 20%)이 나타났다. 본 증례고찰을 통하여 복막투석은 신부전(특히 급성기)에 이환된 개에서 질소혈증을 개선하는데 효과적임을 알 수 있었다.