• Title/Summary/Keyword: Ion-exchange technology

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In Vitro Controlled Release of Piracetam with Coated Ion-Exchange Resin (이온교환수지를 이용한 피라세탐의 in vitro 방출조절)

  • Hwang, Young-Sook;Lee, Kyung-Tae;Seo, Seong-Hoon
    • Journal of Pharmaceutical Investigation
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    • v.29 no.2
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    • pp.105-109
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    • 1999
  • The sustained release of piracetam by complexation with ion exchange resin was prepared. The complex was coated with Eudragit RS100 and their releases in vitro were conducted with various different kinds of medium solution. Dissolution rate increased as ionic strength, acidity and drug concentrations increased and reached its maximal plateau concentration within 5 min. Based on these data, The controlled release of piracetam using ion-exchange piracetam complex coated with Eudragit RS100 could be available.

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A study on the optimization of Ion Exchange Resin operating conditions for removal of KCl from CKD extract (CKD 추출액내 KCl 제거를 위한 이온교환수지 조업조건 최적화 연구)

  • Jang, Younghee;Lee, Ye Hwan;Kim, Jiyu;Park, Il Gun;Lee, Ju-Yeol;Park, Byung Hyun;Kim, Seong-Cheol;Lee, Sang Moon;Kim, Sung Su
    • Journal of the Korean Applied Science and Technology
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    • v.36 no.4
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    • pp.1088-1095
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    • 2019
  • The CKD extract is wastewater from which KCl in CKD has been removed to reuse CKD as a cement raw material, and tried to reuse no extracts due to problems such as wastewater treatment facility expansion. As a result of removing KCl by the ion exchange method, the pH of the extract after ion exchange decreased from 12.7 to less than pH 2, and it was confirmed that H+ of the cation exchange resin was dissolved in the extract through ion exchange. In addition, the selectivity of the ion exchange was removed in the order of Ca2+, K+, it was determined that the increase in the contact time to remove the K+ ions. The batch system had a contact time of 6 times or more, compared to the continuous system, and showed 4 times of K+ removal efficiency and 7 times of Cl- removal efficiency. It was showed by analyzing the pH of the extract that more H+ of the cation exchange resin was extracted than OH- of anion exchange resin as the pH of the extract was changed.

The Nature of Acid-Catalyzed Acetalization Reaction of 1,2-Propylene Glycol and Acetaldehyde

  • Cheng, Chen;Chen, Hui;Li, Xia;Hu, Jianli;Liang, Baochen
    • Korean Chemical Engineering Research
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    • v.53 no.4
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    • pp.463-467
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    • 2015
  • We investigated catalytic activity of ion-exchange resins in acetalization of 1,2-propylene glycol with acetaldehyde. The impacts of reaction variables, such as temperature, reaction time, catalyst loading and feedstock composition, on the conversion of 1,2-propylene glycol were measured. The life of the catalyst was also studied. Furthermore, the reaction kinetics of 1,2-propylene glycol acetalization was studied. It was found that reaction rate followed the first-order kinetics to acetaldehyde and 1,2-propylene glycol, respectively. Therefore, overall acetalization reaction should follow the second-order reaction kinetics, expressed as. Key words: 1,2-propylene Glycol, 2,4-dimethyl-1,3-dioxolane, Ion-exchange Resin, Polyhydroxy Compounds, Acetalization $r=kC^{nA}_AC^{nB}_B=19.74e^{\frac{-6650}{T}}C^1_AC^1_B$.

Studies on Physical Properties of Sulfonpolyimide for Fuel Cell (연료전지용 술폰폴리이미드의 물성 연구)

  • Ko, Jae-Churl;Ahn, Bum-Jong;Park, Young-Goo
    • Journal of the Korean Applied Science and Technology
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    • v.22 no.2
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    • pp.151-156
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    • 2005
  • Many researchers have been focused on polymer electrolyte membrane (PEM) to improve performance of a fuel cell. Sulfonpolyimide with hydrocarbon was synthesized from ODA (4,4-diaminodiphenyl ether), ODADS (4,4-diaminodiphenyl ether-2,2-disulfonic acid), NTDA (1,4,5,8-naphthalenetetracarboxylicdianhydride) and CSA (chlorosulfonic acid). In order to estimate the feasibility as a fuel cell, the performance of sulfonpolyimide was analyzed through a swelling degree, IEC (ion exchange capacity), ion conductivity and TEM (transmission electron microscope). As the results of this performance test, swelling degree, IEC and ion conductivity were 37%, 0.06 meq/g and 0.08 S/cm respectively, when the CSA concentration was 0.4 M. It was thought that sulfonpolyimide could be used as a fuel cell through improvement of electrolyte membrane.

Research Trends in Bipolar Membrane for Water Dissociation Catalysts and Energy Technology Applications (바이폴라막의 물 분해 촉매 및 에너지 기술 응용의 연구 동향)

  • Do-Hyeong Kim;Sang Yong Nam
    • Membrane Journal
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    • v.34 no.1
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    • pp.10-19
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    • 2024
  • The bipolar membrane is an ion exchange membrane consisting of a cation exchange layer, an anion exchange layer, and an interface layer, and is a membrane that generates protons and hydroxide ions based on water dissociation characteristics. Using these properties, research is being conducted in various application fields such as the chemical industry, food processing, environmental protection, and energy conversion and storage. This paper investigated the concept of bipolar membrane, water dissociation mechanism, and water dissociation catalyst to provide a comprehensive understanding of bipolar membrane technology, were investigated. Lastly, we also investigated the bipolar membrane process that has been recently applied to energy technology.

Studies on the Preparation of Anion Exchange Membrane through Blending of the Poly(ethylenimine) and the Poly(vinyl alcohol) (폴리비닐알코올과 폴리에틸렌이민과의 혼합을 통한 음이온교환막의 제조 연구)

  • Kim, Sung-Pyo;Kim, Baek-Kyun;Lee, Hak-Min;Rhim, Ji-Won;Jeong, Sung-Il
    • Membrane Journal
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    • v.20 no.4
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    • pp.335-341
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    • 2010
  • This study focuses on the investigation of the anion exchange membrane through blending poly(ethylenimine) (PEI) and poly(vinyl alcohol) (PVA) varying the mixing ratio. To characterize the resulting membranes, the water content, contact angle, FT-IR, thermal gravimetric analysis, ion exchange capacity, ion conductivity and elastic modulus were measured. The PVA / PEI = 90 / 10 membrane showed the ion conductivity, $5.16{\times}10^{-2}S/cm$ and simultaneously the contact angle, $78.3^{\circ}$. According to TGA measurement, the resulting membranes seemed durable at room temperature. Through the modulus test, the mechanical properties increased with increasing PVA content and apparently the membranes looked very robust.

Drug Release Characteristics of Famotidine-Cationic Exchange Resin Complexes and Their Pharmacokinetics in Rats (파모티딘-양이온 교환수지 복합체의 약물방출 특성 및 흰쥐에서의 체내동태)

  • Shin, Dong-Sun;Song, Woo-Heon;Choi, Young-Wook
    • Journal of Pharmaceutical Investigation
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    • v.27 no.4
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    • pp.313-321
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    • 1997
  • Ion exchange resin complexes of famotidine have been prepared by the reaction of famotidine solution with activated ion exchange resins. Complex formation efficiency between famotidine and ion exchange resin was about $80{\sim}90%$ in average, calculated by HPLC determination. Drug release characteristics from the resin complexes were evaluated by the modified percolation method. Famotidine release was dependent on the type of ion exchange resins. In the case of weakly acidic resin complexes, the cumulative released amount of famotidine was more than 90% for 1hr in pH 1.2 buffer solution. However, in the case of strongly acidic resin complexes, it was less than 5% for 3hr in the same medium. Strongly acidic resins revealed some advantages over weakly, acidic resins for overcoming instability of famotidine in gastric juice. In addition, strongly acidic resin complexes showed controlled release of famotidine in pH 6.8 buffer solution, showing the result of about 60 to 70% of drug release for 5hr. After oral administrations of famotidine-resin complexes to rats as dose of 40 mg equivalent/kg, the pharmacokinetic parameters of famotidine were obtained by model independent analysis and compared with those of famotidine solution or suspension. $C_{max}$ of famotidine-resin complex was lower than that of famotidine solution or suspension. MRT, MAT, and MDT of the complexes were greater than those of famotidine solution or suspension. From these results, it was expected that famotidine was released slowly from the complexes and absorbed continuously into systemic circulation. It was recognized that drug release from the complexes was the rate-limiting step in drug absorption, since there were close correlations between in vitro drug release and in vivo pharmacokinetic parameters.

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Property of ion Exchange Resin having Tripropylamine as Functional Group for Development of Denitrogenation Process

  • Lee, Dong-Hwan;Lee, Yong-Hee;Lee, Kook-Eui;Roh, Jong-Su;Suh, Myung-Gyo
    • Proceedings of the Korean Environmental Health Society Conference
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    • 2005.06a
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    • pp.355-358
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    • 2005
  • Nitrate-selective ion exchange resins involving bulky trialkyl amino as functional group were synthesized by the reaction of chloromethylated polystyrene-divinylbenzene copolymer and the corresponding tripropylamine in ethanol. Fundmental properties such as bulk density, water content, effeative diameter, uniformity coefficient, appearance index, exchange capacity and particle size distribution were fully measured. The synthesized resins appeared to be good for nitrate selection.

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Preparation and Release Characteristics of Dextromethorphan HBr Ion-exchange Albumin Microcapsule (브롬화수소산 덱스트로메토르판의 이온교환 알부민 마이크로캅셀의 제조 및 용출특성)

  • Ahn, Eun-Sun;Ku, Young-Soon;Kim, Kil-Soo
    • Journal of Pharmaceutical Investigation
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    • v.21 no.2
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    • pp.111-116
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    • 1991
  • Dextromethorphan HBr (DMP HBr) ion exchange albumin microcapsules were prepared by the interfacial polymerization method. The incorporation of drugs in empty albumin microcapsules was more increased in case of glutaraldehyde (GA) and formaldehyde (FA) than terephthaloyl chloride (TC) as a cross linking agent. The amount of DMP HBr incorporated into empty albumin micorcapsules was augemented with increasing DMP HBr concentration and the amount of empty microcapsules in the incorporation medium. Increasing the salt concentration in the release medium, the release rate and the DMP HBr amount released from microcapsules were increased. The release rates of DMP HBr from microcapsules retarded considerably compared with DMP HBr powder.

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Formation of surface mediated iron colloids during U(VI) and nZVI interaction

  • Shin, Youngho;Bae, Sungjun;Lee, Woojin
    • Advances in environmental research
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    • v.2 no.3
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    • pp.167-177
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    • 2013
  • We investigated that removal of aqueous U(VI) by nano-sized Zero Valent Iron (nZVI) and Fe(II) bearing minerals (controls) in this study. Iron particles showed different U(VI) removal efficiencies (Mackinawite: 99%, green rust: 95%, nZVI: 91%, magnetite: 87%, pyrite: 59%) due to their different PZC (Point of Zero Charge) values and surface areas. In addition, noticeable amount of surface Fe(II) (181 ${\mu}M$) was released from nZVI suspension in 6 h and it increased to 384 ${\mu}M$ in the presence of U(VI) due to ion-exchange of U(VI) with Fe(II) on nZVI surface. Analysis of Laser-Induced Breakdown Detection (LIBD) showed that breakdown probabilities in both filtrates by 20 and 200 nm sizes was almost 24% in nZVI suspension with U(VI), while 1% of the probabilities were observed in nZVI suspension without U(VI). It indicated that Fe(II) colloids in the range under 20 nm were generated during the interaction of U(VI) and nZVI. Our results suggest that Fe(II) colloids generated via ion-exchange process should be carefully concerned during long-term remediation site contaminated by U(VI) because U could be transported to remote area through the adsorption on Fe(II) colloids.