• 제목/요약/키워드: neutralization titration

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Comparison of Titration Curve Estimation Methods for pH Neutralization Processes

  • Park, Ho-Cheol;Lee, Jie-Tae
    • 제어로봇시스템학회:학술대회논문집
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    • 제어로봇시스템학회 2001년도 ICCAS
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    • pp.124.1-124
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    • 2001
  • Control of pH neutralization process plays a very important role in some chemical process. Because of their high nonlinearity, frequent disturbance, and time-varying characteristics, it is difficult to control and estimate pH processes. For the adaptive control of pH processes, a lot of researchers have made an efforts in the modeling and control of pH processes. It is very difficult to obtain information of influent stream such as concentrations and dissociation constants and the titration curve equation is very complex. Therefore, several simple models, which hate small number of unknown parameters and estimate the titration curve, have been available, These models were considered here and were transformed into forms that can applied the linear least square method.

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산·염기 적정에서 용액의 부피 변화에 대한 대학생들의 오개념 연구 (College Students' Misconception about the Volume Change of Solution during Acid/Base Titration: Partial Molar Volume of Salt)

  • 장낙한
    • 과학교육연구지
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    • 제33권2호
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    • pp.317-320
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    • 2009
  • 부피 측정법을 이용하여 산 염기 적정 실험에서 중화점을 측정할 때, 나는 용액의 부피 변화에 대한 한국 대학생들의 개념을 조사하였다. 이 연구에 의하면, 대부분의 대학생들은 산 염기 적정 동안 중화반응에 의해 물이 생성되기 때문에 부피가 증가한다는 오개념을 갖고 있었다. 그러나 이것은 용액에 있는 염에 의한 효과를 무시한 것이기 때문에, 부피 변화를 설명하는데 충분하지 않다. HCl/NaOH 중화반응 동안 용액의 부피 증가를 설명하기 위해, 나는 생성된 NaCl의 부분 몰부피를 계산하였다. 실험 결과와 계산된 부분 몰부피를 비교할 때, 나는 부피 증가의 주요 효과는 HCl/NaOH 중화반응 동안 생성된 NaCl의 부분 몰부피 때문이라는 것을 밝혔다. 여기서 산 염기 중화 적정 동안 용액의 부피 변화에 대한 오개념을 줄이기 위해, 나는 부분 몰부피의 개념을 대학생들에게 도입하도록 제안한다.

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The Characteristic Calulation of Carboxylic Ion Exchanger.

  • 손원근;김태일;김상헌;박수길;정장훈
    • Bulletin of the Korean Chemical Society
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    • 제22권6호
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    • pp.559-564
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    • 2001
  • A method for calculating the main characteristics of a potentiometric titration curve in a carboxylic ion exchanger has been investigated. The potentiometric titration curves of simple electrolyte and ion exchangers (polyelectrolytes) showed a great difference between them. The acidity parameters of the ion exchangers, the thermodynamic constant (pK0), apparent equilibrium constant (K), and correction for the apparent equilibrium constant (b), were introduced and used to express the characteristics of the carboxylic ion exchanger. A characteristic equation related to the acidity parameters of the ion exchangers systems was derived. A fibrous carboxylic cation exchanger was used and potentiometric titration curves at different concentrations of the supporting electrolyte were obtained . To prove the validity of the characteristic equation, the concentration of the supporting electroyte was varied. In the present study, good agreement between the data points and the fitted curves was found in all the cases. The g (number of moles of alkali to 1 g of ion exchanger) of carboxylic ion exchanger was calculated from the concentration of supporting electrolyte (C), pH of the solution, and degree of neutralization of ion exchanger (x).

SVM을 이용한 비선형 화학공정 모델링: pH 중화공정에의 적용 예 (Nonlinear Chemical Plant Modeling using Support Vector Machines: pH Neutralization Process is Targeted)

  • 김동원;유아림;양대륙;박귀태
    • 제어로봇시스템학회논문지
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    • 제12권12호
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    • pp.1178-1183
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    • 2006
  • This paper is concerned with the modeling and identification of pH neutralization process as nonlinear chemical system. The pH control has been applied to various chemical processes such as wastewater treatment, chemical, and biochemical industries. But the control of the pH is very difficult due to its highly nonlinear nature which is the titration curve with the steepest slope at the neutralization point. We apply SVM which have become an increasingly popular tool for machine teaming tasks such as classification, regression or detection to model pH process which has strong nonlinearities. Linear and radial basis function kernels are employed and each result has been compared. So SVH based on kernel method have been found to work well. Simulations have shown that the SVM based on the kernel substitution including linear and radial basis function kernel provides a promising alternative to model strong nonlinearities of the pH neutralization but also to control the system.

Charge Determination of Humic Acid and Humic Extract by Spectrophotometry

  • Kam Sang Kyu;Cho Eun Il
    • Environmental Sciences Bulletin of The Korean Environmental Sciences Society
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    • 제2권2호
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    • pp.139-148
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    • 1998
  • The charge densities of humic acid and humic extract have been determined by back titration using spectrophotometry as the method of end point detection and several cationic polymers of different charge density(copolymers of acylamide and dimethylaminoethylacrylate and polydiallyidimethylammonium chloride, PDDA), and a cationic indicator o-toluidine blue(o-Tb). The charge densities of humic acid and humic extract obtained depend on the charge densities of cationic polymers used. When the polymers of lower charge density are used, lower apparent charge density values are obtained, but for polymers of high charge density(above 2.5 meq/g), the measured values are almost identical, but also are nearly the same as that obtained for PDDA which has a high charge density(about 6 meq/g). For polymers of lower charge density, it is considered that the optimum dosage does not correspond to 1 :1 charge neutralization between anionic and cationic groups. Polymers of high charge density should be used in order to achieve a complete charge neutralization. As humic acid and humic extract are dissociable acids, their ionization is heavily pH dependent and so higher charge density values are obtaines with increasing pH.

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Heparin-Protamin Sulfate 상호작용의 실험적 연구

  • 김치경;이홍균
    • Journal of Chest Surgery
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    • 제13권1호
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    • pp.13-20
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    • 1980
  • Heparin would have been used for preventing clotting of blood during extracorporeal circulation and subsequent use of protamine sulfate and made possible the neutralization of heparin. This procedure has been adopted for eliminating one of the great causes of bleeding, especially in cardiac surgery. In this experiment, the hypocoagulability of blood induced by heparin followed by neutralization with treatment of protamine sulfate were estimated by the Lee-White clotting time [CT], partial thromboplastin time [PTT] and protamine titration test. The results were as follows: 1] Comparison of clotting time between the heparinized [2.0 mg/kg] and non-heparinized dogs was done using CT and PT`I` of the blood. In heparinized group [Group I], the CT lasted infinitively and prolongation of PTT [4 times than normal] until 60 minutes. The CT [2 times] and PTT [3 times] has been shortened after 90 minutes, however they returned to normal limit level within 180 minutes. 2] The determination of appropriate ratio of heparin and protamine In vivo were performed. The group II [heparin 2.0 mg/kg, protamine 1.0 mg/kg] revealed rapid decrease of CT and PTT, but returned to normal after 120 minutes. The group III [heparin 2.0 mg/kg, protamine 2.0 mg/kg] returned rapidly to normal within 15 minutes. The group IV [heparin 2.0 mg/kg, protamine 3.0 mg/kg] recovered its normal level after 60 minutes. The group V [heparin 2.0 mg/kg, protamine 4.0 mg/kg] recovered its normal level after 90 minutes. 3] In the combined experimental study In vivo and vitro, the protamine titration test was done using the dog which were given 2.0 mg/kg and 3.0 mg/kg of heparin, respectively and coagulation time were checked after 15, 30, 60 and 120 minutes. The complete neutralization was showed to be heparin-protamine ratio of 1:1 to 1.5. 4] In vitro study, fresh blood was drawn into known amount of heparin content [20, 40, 60 and 100/ug per 1 ml of blood] syringe, thereafter protamine titration test was done. In all cases, the complete neutralization was found in heparin-protamine ratio of 1:0.85 to 1.5. 5] It was found by the present experiment that the ideal heparin-protamine ratio was 1:1 within 60 minutes and 1:0.5 after 60 minutes for avoiding the serious side effect due to overadministration of protamine sulfate.

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세 가지 다른 중화적정 실험 방법에 따른 고등학생들의 산.염기 관련 개념의 이해 분석 (Analysis of High School Students' Understanding of Acid-Base Related Concepts Using Three Different Neutralization Titration Technologies)

  • 이종백;박가영;이상권
    • 한국과학교육학회지
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    • 제31권6호
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    • pp.864-875
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    • 2011
  • 이 연구에서는 고등학교 1학년 학생을 대상으로 중 세 가지 다른 중화적정 실험 방법에 따른 고등학생들의 산 염기 관련 개념의 이해 분석 873 화적정 방법에 따른 산 염기 및 중화반응 개념의 이해도를 알아보고자 하였다. 세 개의 집단은 각각 지시 약, pH미터, MBL을 이용하여 중화적정 실험을 하도록 하였다. 각 집단별로 중화적정 실험 수업을 하기 전과 후에 산 염기 및 중화반응 개념 검사를 하여 그 향상 정도를 알아본 후 고등학생들이 산 염기 및 중화반응에 대한 과학적인 개념을 형성하는데 효과적인 실험 방법이 무엇인지 알아보았다. 세 집단 모두 중화적정 실험 수업을 마친 후 사후검사에서 개념 이해에 유의미한 향상이 있었지만 그 중에서도 MBL을 이용한 집단의 향상도가 가장 높았고 pH미터를 이용한 집단의 향상도가 가장 낮았다. 적극적인 동기 유형을 가진 학생들이 소극적인 학생들보다 사전검사 및 사후 검사 점수는 높았지만 평균 점수 차이를 볼 때 소극적인 학생들의 개념 이해의 향상 정도가 더 높은 것으로 나타났다. 적극적인 학습 동기를 갖는 학생들은 개념 이해에 있어서 실험 방법에 의존하지 않지만 소극적인 학생들은 그 차이가 크게 나타났으며 MBL을 사용할 때 가장 높게 나타났다. 인지수준에 따른 개념 이해 정도에서는 인지수준이 높을수록 산 염기 관련 개념 이해 정도가 높았다. 그리고 중화적정 실험 수업을 하기 전과 후의 개념 이해 향상 정도는 과도기를 포함한 구체적 조작기 학생들이 가장 큰 폭으로 상향변화 하였다. 각 집단별 인지수준과 학습동기에 따른 개념 이해를 비교해보면 적정 방법에 따라 향상 정도에 차이가 있었으므로 학습자의 인지수준과 동기 유형에 따라 적절한 실험 방법을 선택해 줌으로써 학생들의 개념 이해의 어려움을 최소화하도록 해야 한다.

혼합제제중 Methylephedrine Hydrochloride와 Ephedrine Hydrochloride의 분리정량에 관한 연구 (Study on Isolative Determination Methylephedrine Hydrochloride and Ephedrine Hydrochloride in the Mixed Preparation)

  • 고인석
    • 생약학회지
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    • 제1권3호
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    • pp.93-99
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    • 1970
  • There have been reported by several workers for the isolation and determination of the amine derivatives as Metbylephedrine Hydrochloride and Ephedrine Hydrochloride adopting neutralization method, steam distillation method, non-aqous titration method, ion-exchange resin method, titration method after acetylation, colorimetric method, gravimetric method, iodine titration method and gas chromatography. Those methods mentioned in above, can be practically applied for the sample which is not mixed one mith the other amine compounds. Presently, it has not shown on the isolative determination of the mixed sample of amine derivatives. In this paper, it is discussed on the isolative determination of Methylephedrine Hydrochloride as the tertiary amine compound and Ephedrine Hydrochloride as the secondary amine compound. According to the results of the experiment, it could be summarized as follows: 1. There is no time-variation on the color reaction of Methylephedrine Hydrochloride and Ephedrine Hydrochloride with the color reagent, bromcresolgreen. And Methylephedrine Hydrochloride and Ephedrine Hydrochloride, respectively, can be determined spectrophotometrically by means oft his color reaction. 2. For the isolation of Methylephedrine Hydrochloride and Ephedrine Hydrochloride from the mixed sample, Methylephedrine Hydrochloride can be eluted by chloroform, while Ephedrine Hydrochloride by the mixed solvent of chloroform and ethylalcohol (2:1), from the celite column adsorbed at pH6.4 followed by extraction with ether undersodium hydroxide alkali re action. 3. When the sample is mixed with quinine hydrochloride, dihydrocodeine bitartate, and noscapine, these mixed compounds can be eliminated by means of stram distillation. 4. When the sample is mixed with chlorpheniramine maleate, dextromethorphan hydrobromide and diphenhydramine hydrochloride, the mixed compounds can be eliminated by means of steam distillation and celite adsorption column chromatography, In conclusion, the isolative determination method for Methylephedrine Hydrochloride and Ephedrine Hydrochloride studied in this paper, indicates with the excellent reproducibility and accuracy.

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전위차 적정법을 이용한 인산형 양이온교환수지의 특성 계산 (The Characteristic Calculation of a Phosphoric Acid Ion Exchanger using the Potentiometric Titration)

  • 김태일;손원근
    • 공업화학
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    • 제10권6호
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    • pp.871-875
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    • 1999
  • 인산형 양이온교환수지 특성 계산과, 이온교환수지의 전위차 적정곡선의 형태에 따른 정확한 이온교환용량을 결정할 수 있는 방법을 알아보았다. 이온교환수지는 divinylbenzene 4%로 가교화된 polystyrene 공중합체를 인산화한 것으로 이온교환용량이 5.7 meq/g이다. 인산형 양이온교환수지는 직선의 식으로 설명할 수 있었고, 직선 기울기로부터 적정시 zero중화와 완전중화사이의 평형상수 음의 대수(pK) 값의 차인 ${\Delta}pK$의 값을 구할 수 있었으며, ${\mathit{x}}=0.5$에서 얻어진 실험 및 이론의 pK값이 잘 일치하는 것을 알 수 있었다. 이온교환수지의 전위차 적정곡선은 NaOH나 $Ba(OH)_2$로 적정할 때 ${\mathit{x}}$의 변화에 따른 pK의 실험 값과 계산 값이 잘 일치하는 것을 알 수 있었다. 전위차 적정곡선의 변곡점은 원자가가 1가인 이온보다는 2가 이온이 크게 변화되는 것을 알 수 있었으며, g값과 도함수 ${\partial}pH/{\partial}g$의 관계를 Lorentz함수로서 나타내어 더욱 정확한 이온교환용량을 결정할 수 있었다.

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