• Biotechnology and Bioprocess Engineering:BBE
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• 제11권2호
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• pp.110-115
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• 2006

We conducted a sensitivity analysis of the simulated moving bed (SMB) chromatography with the case model of the separation of two amino acids phenylalanine and tryptophan. We consider a four-zone SMB chromatography where the triangle theory is used to determine the operating conditions. Competitive Langmuir isotherm model was used to determine the adsorption isotherm. The finite difference method is used to solve nonlinear partial differential equation (PDE) systems numerically. We examined the effects of alterations in the operating conditions(feed-extract, feed-raffinate, eluent-extract, eluent-raffinate, recycle, and switching time) and the adsorption isotherm parameters (Langmuir isotherm parameters a and b) on SMB efficiency. The variation range of operating conditions and Langmuir isotherm a was between -50 and 50% of original value and the variation range of the Langmuir isotherm b was between $2.25^{-5}$ and $2.25^5$ times of original value.

• 대한화학회지
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• 제8권2호
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• pp.62-64
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• 1964

The cation exchange chromatographic studies for the analysis of transition metals have been described. The quantitative separation of a mixture of Fe(Ⅲ), Cu(II), Zn(II), Ni(II), Cd(II), Co(II) and Mn(II) has been obtained by elution, through a 28cm column of the resin, Dowex 50 ${\times}$ 4 (100∼200 mesh), using 0.45 M $NaNO_3$+0.05 M Na-tartrate solution as eluent, starting with the eluent of pH 3.5, followed stepwise by pH 4.0 and 4.5. A comparison between the calculated and the observed peak positions in the elution curve has been shown. The relative stability constants for tartrate complexes of some transition metals have been calculated by using distribution ratios obtained in this separation procedure.

• Bulletin of the Korean Chemical Society
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• 제4권2호
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• pp.76-79
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• 1983

The elution behaviors of a series of metal complexes, such as $Co(gly)_{3}$, $[Ni(en)_{3}]^{2+}$, $[Ni(phen)_3]^{2+}$, $[Fe(phen)_3]^{2+}$, $[Co(phen)_3]^3+$, $[Co(tn)_3]^3+$, $[Co(en)_3]^3+$ and $[Co(NH_3)_6]^3+$ (where gly; glycine, phen; phenanthroline, tn; trimethylenediamine, en; ethylenediamine), were studied in aqueous solution by measuring the retention volumes (v values) on SP-Sephadex C-25, cation exchange resin. It was found that the elution behaviors of metal complexes were apparently affected by salt concentrations, kinds of cations in eluent and kinds of anions in eluent, and according to the degrees of their effects coulombic forces, ion exchange capacities, the 'solvent effect' of resin backbone, hydrophobicity and hydrophilicity were applied to explain the elution mechanism.

• Bulletin of the Korean Chemical Society
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• 제13권3호
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• pp.285-289
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• 1992

Enantiomeric separation of underivatized amino acids using N-alkyl-L-proline (octyl, dodecyl or hexadecyl) coated HPLC has been accomplished. The anchoring N-alkyl groups of L-proline provides a permanent adsorption of there solving chiral agent on the hydrophobic interface layer of a reversed phase. The factors controlling retention and enantioselectivity such as the Cu(II) concentration, pH of the eluent, the type and concentration of organic modifier in the hydroorganic eluent, and extent of coating were examined. The elution orders between D- and L-amino acids were consistent, L-forms eluting first, except histidine and asparagine. The extremely high enantioselectivity $(\alpha$ upto 13 for proline) is observed. The retention mechanism for the chiral separation can be illustrated by a complexation and hydrophobic interaction.

• 대한화학회지
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• 제28권1호
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• pp.47-53
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• 1984

DTPA 용리액의 pH와 농도를 변화시키면서 음이온 교환수지관을 이용해서 희토류 원소들을 분리하는 연구를 하였다. 희토류 원소들의 가장 좋은 분리조건은 0.025M DTPA, pH 8.35이 있었으며 희토류 원소들의 용리순서는 Sm을 제외하고 희토류 원소들의 원자번호 순서와 일치하였다. 0.025M DTPA, pH 8.35에서 분리한 인접 희토류 원소들의 분리값은 3.03~1.25이었으며 그중 Ce/Pr이 3.03으로 최대값을,Eu/Gd은 최소값을 각각 갖는다. 0.025M DTPA 희토류 원소들을 용리하였을 때, pH 8.0~8.6의 넓은 범위에서 비교적 좋은 분리현상을 보였다.

• 대한전자공학회:학술대회논문집
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• 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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• pp.337-341
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• 2001

A new method to extract gold from pyrite roster cinder, which combines ultra-fine-grinding with resin-in-pulp, has been studied in this paper. Compared with traditional leaching technology, it can short leaching time, avoid complex filter process, lower sodium cyanide consumption and increase gold recovery by 35%. During leaching, aluminium oxide ball was used as stirred medium, hydrogen peroxide as leaching aid and sodium hexametaphosphate as grinding aid. With the high efficiency and chemistry effect of ultra-fine-grinding, the leaching process was developed and the gold leaching rate may reach 88%. With AM-2 Б resin as abosorber and sulfocarbamide (TU) as eluent, gold was recovered from cyanide pulp by resin-in-pulp. AM-2 Б resin has good adsorbability in cyanide solution(pH=10). It was easy to elude gold from the loaded resin with 0.1㏖/L cholhydric acid and 1㏖/L sulfocabamide. The effect of contact time, temperature and acidity etc. on the gold absorption had been examined with static methods. The results showed that the adsorption and desorption of gold could both reach over 98%. The effects of flow rate of solution on dynamic adsorption and elution of gold had been examined with dynamic methods. Breakthrough curve and elution curve had been drawn in this paper. A mild condition was determined through a number of experiments: leaching time 2 hours, liquid solid ratio 4:1, sodium cyanide 3kg/t, hydrogen peroxide 0.05%, sodium hexametaphosphate 0.05%; adsorption time 30 minutes, temperature 10-3$0^{\circ}C$, resin($m\ell$) solid(g) ratio 1:10, eluent resin ratio 10-20:1, velocity of eluent $1.5m\ell$/min. Under the mild condition, the gold recovery may reach 85%.

• 대한화학회지
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• 제35권5호
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• pp.553-559
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• 1991

$NH^{4+}$ retaining 이온으로 치환된 양이온교환 수지관에서 흡착시키는 희토류원소이온의 양, 수지관의 내경, 수지관의 길이 및 용리액의 pH 등을 변화시켜 용리시킨 후 용출액 중의 각 화학종을 분석하여 희토류원소이온의 용리 mechanism과 monazite 광에 포함된 희토류원소들의 분리에 관해 연구하였다. 인접한 희토류원소간의 분리능은 수지의 교환용량 이내에서는 흡착시키는 희토류원소이온의 양을 증가시킬수록 증가하였고, 내경이 같으면 수지관의 높이는 희토류원소이온의 분리능 및 분리시간에 영향을 미치지 않으며 희토류-EDTA 착물은 $NH^{4+}$형 수지에 흡착되지 않음을 알 수 있었다. 용리액의 pH는 수지관 내에서 희토류원소이온과 EDTA와의 반응성에 영향을 미쳐 분리에 큰 영향을 미쳤으며 pH가 낮을수록 분리능은 향상되나 분리시간이 길어짐을 알 수 있었다.

• Journal of Periodontal and Implant Science
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• 제26권4호
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• pp.889-905
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• 1996

It is known that growth factors function as potent biologic mediators regulating numerous activities of wound healing via cell proliferation, migration and extracellular matrix formation and they also promote periodontal regeneration. But, method of growth factor application is controversial yet. So purpose of this study is to evaluate the effect of demineralized root surface as one of method of growth factor application. The ginigival fibroblasts were primary cultured and fifth or sixth subpassages were used in these experiments. In first experiment, root surface blocks demineralized with 100mg/ml tetracycline for 5 minutes and pH 1 citric acid for 3 minutes(experimental groups) and nonteminerilized root surface blocks (control groups) were placed in 100ng/ml PDGF-BB for 5 minutes. Then the cells were seeded on each root surface blocks and cultured for 6, 24, 48, 72 hours. In second experiment, root surface blocks deminerilized with tetracycline and citric acid and nondemineralized root surface blocks were placed in 200ng/ml PDGF-BB for 5 minutes and another non-demineralized root surfcae blocks were placed in DMEM without PDGF-BB. At 1, 2, 4, 6, 8 days, the cells were seeded in 24-well plate and using of each eluent, cultured for 72 hours. The results of the four determinants were presented as mean and S.D.. The results were as follows : The attachment and proliferation of human gingival fibroblast on root surface were more increased when PDGF-BB was applicated on root surfrace demineralized with tetracycline or citric acid than non-demineralized root surface. And, in comparision tetracycline with citric acid, there were more attachment and proliferation of human gingival fibroblast on root surface demineralized with tetracycline than citric acid, and proliferation of human gingival fibroblast on demineralized root surface was increased time dependently 1 day to 3 days. In second experiment using eluent, proliferation of human gingival fibroblast was more increased to 6 days when human gingival fibroblast was cultured in eluent that PDGF-BB was applicated on demineralized root surface than two control groups, and degree of proliferation was decreased time dependently 1 day to 6 days. Proliferation of human gingival fibroblast cultured in eluent without PDGF-BB was constant 1 day to 6 days. After 6 days, degree of proliferation of human gingival fibroblast was similar in four groups. This means that release duration of PDGF-BB from demineralized root surface is 6 days. And in comparision tetracycline with citric acid, there was more proliferation of human gingival fibroblast in tetracycline-treated group than citric acid. In conclusion, demineralized root surface as primary site for PDGF-BB application, especially demineralized with tetracycline has important roles in attachment and proliferation of human gingival fibroblast, and may be useful clinical applications in periodontal regenerative procedures.

• 한국산림과학회지
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• 제87권2호
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• pp.260-269
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• 1998

본 연구는 전통적인 민간요법으로 많이 이용되고 있는 옻나무의 옻칠액의 주성분인 urushiol의 암세포증식억제 효과를 검정하기 위하여 L1210(mouse 혈액암세포), PC-9(인체폐암세포), A427(인체폐암세포), KATO III(인체위암세포)에 대한 urushiol의 세포독성을 검정하였다. Urushiol은 column chromatography에서 hexane과 acetone을 혼합하여 step-wise법으로 용출한 분획을 암세포주 L1210, PC-9, A427, KATO III에 투여했다. 그 결과 암세포 증식억제효과는 hexane : acetone(9 : 1) 분획이 가장 높았고, 그외 50%억제농도($IC_{50}$)는 A427 에서 $0.018{\mu}g/m{\ell}$로 가장 우수하였다. 이들 암세포에 대한 urushiol의 hexane: acetone(9 : 1)분획의 50%억제농도($IC_{50}$)를 시판용 tetraplatin 비교한 결과 urushiol이 tetraplatin에 대하여 L1210에서 3.4배, PC-9 에서 3.9배, A427에서 105.5배의 낮은 농도에서도 동일한 억제효과를 나타냈고, KATO III에서는 다소 높았다.

• 분석과학
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• 제10권1호
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• pp.53-59
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• 1997

$Cl^-$형 음이온 교환수지에서 희토류-EDTA 용리액을 사용하여 희토류 원소 혼합물 중의 원하는 한 원소를 분리 회수하는 연구를 하였다. 음이온 교환수지에 $Sm^{3+}$, $La^{3+}$, $Ce^{4+}$의 EDTA-착물을 흡착시키고, Sm-EDTA 용액으로 용리시키면, 수지에 흡착된 희토류 원소 중 $Sm^{3+}$ 외의 희토류 원소는 용리된다. 수지에 남아 있는 $Sm^{3+}$는 단계적으로 1M HCl 용액으로 용리시켜 분리하였다. Sm-EDTA 용액 대신 La-EDTA 용액으로 용리시키면 $Sm^{3+}$과 $Ce^{4+}$이 $La^{3+}$과 같이 용리되어 완전한 분리가 되지 않았고, Ce-EDTA 용액으로 용리시킬 때도 분리가 불가능하였다. Sm-EDTA 용액으로 용리시킬 때 용리 구조는 다음과 같다. 흡착과정 : $RCl+Ln-Y^-{\leftrightarrows}RLnY+Cl^-$, Sm-EDTA 용리 : $RLnY+Sm-Y^-{\leftrightarrows}RSmY+Ln-Y^-$, HCl 용리 : $RSmY+HCl{\leftrightarrows}RCl+Sm-Y^-$.