• 제목/요약/키워드: Ion exchange model

검색결과 117건 처리시간 0.019초

천연 제올라이트와 제올라이트 담체를 이용한 NH4+-N 이온교환 특성 평가 (Evaluation of NH4+-N Ion Exchange Property using Natural Zeolite and Zeolite Carrier)

  • 이광현;박민석;주현종
    • 한국물환경학회지
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    • 제25권5호
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    • pp.750-757
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    • 2009
  • The ammonium ion exchange characteristics of natural zeolite were investigated to remove ${NH_4}^+-N$. The effect of water temperature, particle size and competitive cation on the exchange capacity was examined. Ammonium ion exchange capacity tended to decrease when the temperature increased from $25^{\circ}C$ to $40^{\circ}C$. Exchange capacity was increased according to the particle size of natural zeolite comes to be small. Batch isotherm experiments were conducted for measuring ammonium ion exchange capacity. The ion exchange capacity was well described either by the Langmuir isotherm model or by the Freundlich isotherm model. The ammonium ion exchange capacity ($q_m$) of zeolite carrier can be calculated $11.744mg-{NH_4}^+/g$-carrier. The ion exchange capacity of manufactured zeolite carrier was showed a similar tendency as ion exchange capacity of powder-sized natural zeolite. Therefore, zeolite carrier can be used for increasing of nitrogen removal efficiency in the wastewater treatment plants.

연속이온교환평형 칼럼 모델 개발 (Development of Column ion Exchange Modeling with Successive Ion Exchange Equilibrium)

  • 이인형
    • 한국산학기술학회논문지
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    • 제3권2호
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    • pp.141-145
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    • 2002
  • 이온교환수지탑으로 유입된 이온은 연속적인 이온교환 평형을 이루면서 수지층을 통과한다는 가정하에 질량작용법칙과 몰 균형식을 조합하여 연속이은교환평형 칼럼모델을 개발하였다. 연속이온교환평형 칼럼모델을 이용하여 원자력발전소 복수탈염설비 탈염기의 성능을 평가한 결과, Na/sup +/및 Cl/sup -/누출 농도는 수지의 재생효율에 따라 다르며, 특정이온의 유입수 및 유출수에서 농도 비율은 용액 및 수지의 상태에 따라 달라짐을 확인하였다. 본 모델은 수지농도를 보정하여 국부 불완전 평형을 고려할 수 있고, 다성분 존재하의 경쟁적 이온교환을 묘사할 수 있는 장점을 가지고 있다.

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Decontamination of spent ion exchange resins contaminated with iron-oxide deposits using mineral acid solutions

  • Tokar, E.A.;Matskevich, A.I.;Palamarchuk, M.S.;Parotkina, Yu.A.;Egorin, A.M.
    • Nuclear Engineering and Technology
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    • 제53권9호
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    • pp.2918-2925
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    • 2021
  • The efficiency of decontamination of model spent ion exchange resins, contaminated with magnetite and hematite, with mineral acid solutions, and using electro-decontamination, was evaluated. It has been shown that effective hematite dissolution occurs in concentrated mineral acid solutions. However, the use of direct current increases the decontamination efficiency of spent ion exchange resins contaminated with hematite. It is determined that with increasing voltage and acid concentration, the dissolution efficiency of hematite deposits increases and can exceed 99%. It has been shown that hematite dissolution is accompanied by secondary adsorption of radionuclides due to ion exchange, which can be removed with sodium nitrate solutions.

A Numerical Solution of Transport of Mono- and Tri-valent Cations during Steady Water Flow in a Binary Exchange System

  • Ro, Hee-Myong;Yoo, Sun-Ho
    • Journal of Applied Biological Chemistry
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    • 제43권1호
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    • pp.18-24
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    • 2000
  • A one-dimensional transport of displacing monovalent ion, $A^+$, and a trivalent ion being displaced, $B^{3+}^ in a porous exchange system such as soil was approximated using the Crank-Nicolson implicit finite difference technique and the Thomas algorithm in tandem. The variations in the concentration profile were investigated by varying the ion-exchange equilibrium constant (k) of ion-exchange reactions, the influent concentrations, and the cation exchange capacity (CEC) of the exchanger, under constant flux condition of pore water and dispersion coefficient. A higher value of k resulted in a greater removal of the native ion, behind the sharper advancing front of displacing ion, while the magnitude of the penetration distance of $A^+$ was not great. As the CEC increased, the equivalent fraction of $B^{3+}^ initially in the soil was greater, thus indicating that a higher CEC adsorbed trivalent cations preferentially over monovalent ions. Mass balance error from simulation results was less than 1%, indicating this model accounted for instantaneous charge balance fairly well.

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질량작용법칙과 표면착화모델을 이용한 이온교환 모델링 (Ion Exchange Modeling with Mass Action Law and Surface Complexation Models)

  • 안현경;김상대;이인형
    • 한국산학기술학회논문지
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    • 제4권3호
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    • pp.296-300
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    • 2003
  • 다성분 양이온 교환을 위한 평형과 동역학 데이터는 질량 작용 법칙과 표면 착화 모델을 이용하여 수행 및 평가하였다. 양이온 흡착의 평형과 칼럼 실험은 양이온 교환 합성 수지 IRN 77로 H/sup +/, Li/sup +/, Na/sup +/, NH₄/sup +/, Mg²/sup +/ 이용하여 2, 3, 4, 5 성분 양이온 교환을 수행하였다. 질량 작용 법칙과 표면 착화 모델은 이온 선택도와 경쟁적 양이온 교환을 조사하기 위하여 데이터에 대해 시험하였다. 표면 착화 모델은 질량 작용 모델보다 평형과 동역학 실험 데이터를 정확히 예측하였다.

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A Comparative Analysis of Pseudophase Ion-Exchange (PIE) Model and Berezin Pseudophase (BPP) Model: Analysis of Kinetic Data for Ionic Micellar-mediated Semi-ionic Bimolecular Reaction

  • Cheong, May-Ye;Ariffin, Azhar;Khan, M.Niyaz
    • Bulletin of the Korean Chemical Society
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    • 제28권7호
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    • pp.1135-1140
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    • 2007
  • Pseudo-first-order rate constants (kobs) for the reaction of N-benzylphthalimide (NBPT) with HO- have been determined at 2.0 × 10?4 M NBPT, 1.0 × 10?3 and 2.0 × 10?3 M NaOH as well as varying concentrations of cetyltrimethylammonium bromide ([CTABr]T = 0.0-1.7 × 10?1 M). The effects of [CTABr]T ? CMC (with CMC representing the critical micelle concentration of CTABr) on kobs have been analyzed in terms of Berezin's pseudophase (BPP) model and pseudophase ion-exchange (PIE) model. Although both models give the best observed data fit with least-squares values not significantly different from each other, the calculated values of KS from BPP model appear to be more reliable compared to those from PIE model because the values of KS from BPP model are similar to the corresponding KS values determined spectrophotometrically.

이온교환법에 의한 탈질소 공정개발의 기초연구(III) - 회분식 반응기에서의 반응속도론- (Basic Study for Development of Denitrogenation Process by Ion Exchange(III) - A kinetic study in the batch reactor -)

  • 채용곤;이동환;김승일;윤태경;홍성수;이민규
    • 한국환경과학회지
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    • 제9권2호
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    • pp.165-171
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    • 2000
  • A kinetic study for anion exchange was performed for commercially available Cl- type anion exchange resin in use to remove nitrate in water. The obtained results from the batch reactor were applied to the Langmuir and Freundlich models. The constants for Lagmuir model were qmax =29.82 and b=0.202, and for Freundlich model were K=5.509 and n=1.772. Langmuir model showed betterfit than Frendlich model for the experimental results. Ion exchange reaction rate was also calculated and the the approximate first-order reaction, rate constant k1 was 0.16 L/mg.hr. Effective diffusion coefficient was obtained in the range from $9.67$\times$10^{-8} cm^2/sec$ for initial concentration change, and from $6.09$\times$10^{-7} to 3.98$\times$10^{-6} cm^2/sec$ for reaction temperature change. Activation energy during the diffusion was calculated as 26 kcal/mol.

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Adsorption Behaviors for Strontium and Cesium Ions Using Composite Ion Exchangers

  • Kim, H.T.;Han, H.S.;Shul, Y.G.;Moon, J.K.;Oh, W.Z.;Lee, E.H.
    • 한국방사성폐기물학회:학술대회논문집
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    • 한국방사성폐기물학회 2004년도 Proceedings of the 4th Korea-China Joint Workshop on Nuclear Waste Management
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    • pp.1-11
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    • 2004
  • PAN-4A composite ion exchanger was more selective for Sr ion than other cations and PAN-KCoFC composite ion exchanger has much higher ion exchange capacity for Cs ion than other cations. The ion exchange capacities obtained from Dubinin-Polanyi equation were 3.93 meq/g for Sr ion and 1.50 meq/g for Cs ion using PAN-4A and PAN-KCoFC ion exchangers, respectively. The modified Dubinin-Polanyi model fit the experimental data accurately in multi-component system. The effective surface diffusivities $(D_{s, cff})$ for Sr and Cs ions of PAN-4A and PAN-KCoFC ion exchangers were slightly increased with the different particle sizes.

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Preparation for Protein Separation of an Ion-Exchange Polymeric Stationary Phase Presenting Amino Acid and Amine Units Through Surface Graft Polymerization

  • Choi Seong-Ho;Lee Kwang-Pill;Shin Chang-Ho
    • Macromolecular Research
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    • 제13권1호
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    • pp.39-44
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    • 2005
  • Ion-exchange polymeric stationary phases presenting amino acid and amino groups were prepared by the surface grafting of glycidyl methacrylate onto a silica gel surface and subsequent amination. Three kinds of amino acids-L-arginine (Arg), D-lysine (Lys), and D-histine (His)-were used in this study. An ion-exchange polymeric stationary phase presenting ethylene diamine (EDA) was also prepared by surface graft polymerization. Separation of the model proteins bovine serum albumin (BSA), chick egg albumin (CEA), and hemoglobin (Hb) was performed using the amino acid- and amine-derived columns. In separating the CEA/BSA mixture, the resolution time of BSA was longer than that of CEA when using the EDA column, whereas the resolution time of BSA was shorter than that of CEA when using the Arg, Lys, and His columns. In the separation of the Hb/BSA mixture, the resolution time of BSA was longer than that of Hb in the EDA column, whereas the resolution time of BSA was shorter than that of Hb in the amino acid columns (D-Lys, L-Arg, and D-His).

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

  • 신동선;송우헌;최영욱
    • Journal of Pharmaceutical Investigation
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    • 제27권4호
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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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