• 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).

• 환경위생공학
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• 제21권4호
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• pp.29-38
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• 2006

This study included the development of analytical method for determining perchlorate in water sample. The analytical condition was referred in EPA 314.0 method which use ion chromatography and the concentrator column was replaced by the guard column. Concentrating 10mL raw or treated water sample on to AGl6 guard column made it possible to get the LOD(Limit of Detection) of $0.73\;{\mu}g/L$. The total run time was 11 minutes and during run time next sample could be concentrated on AGl6 guard column. Compared to the Concentration method which needed manual operation, the Direct Injection method could screen the many water samples. The LOD of the Direct Injection method was higher and the sensitivity was lower than that of the Concentration method. The RSDs(Relative Standard Deviations) were lower than 2.5 % for peak height and 0.7 % for retention time in pre-concentration methods. This method Showed good reproducibility and reliability and it was thought the deviations of recovery value could be reduced by considering column capacity and making water sample homogeneous. Matrix Elimination could be done using the pre-concentration method if perchlorate were in complex matrix of sample.

• Bulletin of the Korean Chemical Society
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• 제31권8호
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• pp.2201-2206
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• 2010

To improve the separation property and stability of metal chelate Cu(II) column, three new kinds of multidentate aminocarboxy silica columns with cation-exchange properties were synthesized using glutamic acid (Glu), glutamic acidbromoacetic acid (Glu-BAA), glutamic acid-bromosuccinic acid (Glu-BSUA) as ligands and silica gel as matrix. The standard proteins were separated with prepared chromatographic columns. The stationary phases exhibited the metal chelate property after fixing copper ion (II) on the synthesized multidentate ligand silica columns. The binding capacity of immobilized metal ion was related with the dentate number of multidentate ligands. Chromatographic behavior of proteins and the leakage of immobilized metal ion on multidentate chelate Cu(II) columns were affected by the dentate number of multidentate ligands and competitive elution system directly. The results showed that quinquedentate Glu-BSUA-Cu(II) column exhibited better chromatographic property and stability as compared with tridentate Glu-Cu(II) column, tetradentate Glu-BAA-Cu(II) column and commonly used IDA-Cu(II) column.

• 청정기술
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• 제8권4호
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• pp.217-222
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• 2002

본 연구에서는 수직 원통형 충전반응기(packed-bed column reactor)내에 균체가 고정화된 Ca-alginate bead를 넣어 카드뮴이온을 제거하는데 있어 반응기내로 유입되는 유속, 초기농도 등에서 카드뮴 이온($Cd^{2+}$) 제거하는데 최적 조건을 찾고자 하였다. 사용된 균주(Pseudomonas aeruginosa ATCC 27853)는 한국과학기술원 유전공학센터 유전자은행(KCTC)으로부터 구입하였고, Bead로 사용된 Ca-alginate bead는 Sodium Alginate에 균체와 $CaCl_2$를 섞어 제조한 것을 사용하였다. 실험 결과 동일조건일 때 유속이 30 mL/hr > 45 mL/hr > 60 mL/hr의 순서로 제거율이 좋았고 유입속도의 변화에도 불구하고 각 유속에서 50 ppm > 100 ppm > 200 ppm > 300 ppm의 순으로 좋은 제거율을 보였다.

• Bulletin of the Korean Chemical Society
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• 제20권2호
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• pp.223-225
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• 1999

• 분석과학
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• 제20권3호
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• pp.255-260
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• 2007

A new method for the simultaneous determination of low molecular weight amines and quaternary ammonium ions based on the separation by IC with a suppressor and the detection by MS with ESI has been developed. The method has been applied to the analysis of a mixture containing tetramethylammonium ion, tetraethylammonium ion, tetrapropylammonium ion, triethanolamine, trimethylamine and triethylamine. The constituents were separated by isocratic elution using an IonPac CS17 column, a cation-exchange column, and detected by conductivity and mass spectrometry. The newly developed method for the six components demonstrated that the repeatability in terms of relative standard deviation for three measurements was in the range of 0.1-0.5 %. The detection limits were between 0.2 and $0.9{\mu}g/mL$ by the IC/ESI-MS.

• Nuclear Engineering and Technology
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• 제34권1호
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• pp.1-8
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• 2002

After kaolin clay was artificially contaminated with Co$^{2+}$ ion, the remediation characteristics were analyzed by the electrokinetic method. Ethanoic buffer was injected in the soil column and $CH_3$COOH was continuously inputted to the cathode reservoir to restrain the pH increase. Since the pH of the cathode side of the soil column was 4.0 initially and increased to only 6.5 after remediation for 43.6 hours, precipitate, Co(OH)$_2$, was not formed in the column. The effluent rate increased with the passage of time and Co$^{2+}$ removal in the column at the initial time were mainly controlled by ion migration. 13.1% of the total amount of Co$^{2+}$ in the soil column was removed in 10 hours, 46.8% of the total Co$^{2+}$ in 20.8 hours, 71.7% of the total Co$^{2+}$ in 30.1 hours, and 94.6% of the total Co$^{2+}$ in 43.6 hours. Meanwhile, residual concentrations in the column calculated by the developed model were similar to those by experiment. experiment.

• 분석과학
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• 제12권2호
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• pp.89-93
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• 1999

적은 양의 시료를 분석할 수 있는 마이크로 컬럼 이온 크로마토그래피용 전도도 셀과 억압컬럼을 개발하였다. 안지름이 작은 모세관 컬럼을 사용하는 경우 이동상의 유속은 보통 $5{\sim}20{\mu}L/min$ 정도 된다. 따라서 이 경우 일반적인 전도도 셀은 사용할 수가 없기에 내부 부피가 작은 모세관 컬럼용 전도도 셀과 억압컬럼을 제작하였다. 전도도 셀은 두 개의 백금 피하주사 바늘을 안지름이 0.010 mm인 튜브 속에 넣어 간격이 $2{\mu}m$ 되게 만들었고, 억압컬럼은 Nafion 튜브를 이용하여 막-억압컬럼 형태로 개발하였다. 이 전도도 셀과 억압컬럼을 이용하여 실제 음이온들(플루오르화물, 아질산염, 질산염, 염소산염)을 분석한 결과 재현성 있고 양호한 크로마토그램을 얻었다.

• 한국식품과학회지
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• 제24권6호
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• pp.616-618
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• 1992

본 연구에서는 효과적으로 이용하지 못하는 굴박신액에서 이온교환 크로마토그라피로 taurine의 분리하고자 하였다. Dowex 50W $H^+$형과 Dowex 2 OH 형으로 처리한 용출액 중 흡광도가 높게 나타난 획분을 Amberite IRA-410 $OH^-$형에 다시 용출시켜 taurine을 흡착시킨 후 흡착한 taurine을 0.1M acetic acid로 용출시키면 수율과 순도가 84.8%와 94.9%인 taurine을 얻을 수 있었다.

• Journal of Microbiology and Biotechnology
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• 제17권9호
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• pp.1527-1532
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• 2007

Lysine produced during microbial fermentation is usually recovered by an ion-exchange process, in which lysine is first converted to the cationic form (by lowering the pH to less than 2.0 with sulfuric acid) and then fed to a cationexchange column containing an exchanger that has a sulfone group with a weak counterion such as NH;. Ammonia water with a pH above 11 is then supplied to the column to displace the purified lysine from the column and allow its recovery. To enhance the adsorption capacity and for a possible reduction in chemical consumption, monovalent lysine fed at pH 4 was investigated in comparison with conventional divalent lysine fed at pH 1.5. The adsorption capacity increased by more than 70% on a mass basis using pH 4 feeding compared with pH 1.5 feeding. Lysine adsorbed at pH 4 started to elute earlier than that adsorbed at pH 1.5 when ammonia water was used as the eluant solution, and the extent of early elution became more notable at lower concentrations of ammonia. Moreover, the elution of monovalent lysine fed at pH 4 displayed a stiffer front boundary and higher peak concentration. However, when the ammonium concentration was greater than 2.0 N, complete saturation of the bed was delayed during adsorption and the percent recovery yield from elution was lowered., both drawbacks that were considered inevitable features originating from the increased adsorption of monovalent lysine.