• 대한화학회지
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• 제34권6호
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• pp.582-592
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• 1990

양이온 교환체 (LC-18 coated with $C_{20}H_{41}SO_4^-$)에서 희토류원소-$\alpha$HiBA 착물계의 머무름 거동을 연구하였다. [Na$^+$] 및 [$\alpha$-HiBA]의 등용매 또는 기울기 용리에 따른 희토류원소의 머무름을 나타내는 관계식을 이온 교환 평형식으로부터 유도하였다. [$Na+$] 및 [$\alpha$-HiBA]의 등용매 용리에 따른 크기성질(k')의 관계인 log k' vs log [$Na^+$] 및 log k' vs log [$\alpha$-HiBA]의 직선의 기울기 값에 대한 실험값과 계산값을 비교한 결과 서로 일치하였다. 위의 관계식으로부터 비선형 최소자승법으로 각 개별 착물들의 크기성질($k'_{Ln}^{3+}, k'_{LnL}^{2+}, k'{LnL2+}) 및 착물의 안정도 상수(${\beta}_1$, ${\beta}_2$, ${\beta}_3$)를 각각 구하였다. 희토류원소들의 크기성질(k')에 대한 실험값과 계산값의 상관계수가 0.9996보다 좋은 결과를 나타내었다.

• 폴리머
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• 제30권4호
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• pp.305-310
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• 2006

전자선 전조사를 이용하여 PE/PP와 PET 복합섬유 기재에 스티렌을 그래프트 공중합하여 복합양이온 교환 섬유를 합성하였다. 공중합체의 그래프트율은 스티렌 단량체의 농도가 80%일때 123%이었으며 설폰화율은 스티렌 농도 70%에서 3.3 mmol/g 이었으며 그 이후에서는 큰 변화가 없었다. 또한 섬유의 인장강도는 기재에 비해 모두 낮게 나타났으며, 공중합체보다 이온교환 섬유의 인장강도가 최대 $0.206kgf/mm^2$ 로 낮게 나타났다 이온교환 섬유의 칼슘 및 마그네슘 이온에 대한 흡착파과 시간은 pH, 온도가 증가할수록 길어졌으며, 혼합 용액의 경우 단일 용액에 비해 마그네슘의 흡착파과가 늦게 나타났다. 한편 칼슘 및 마그네슘에 대한 반응속도 상수는 각각 0.012, 0.011 L/mg.h 이었으며, 최대 이온교환 흡착용량은 각각 47.06, 42.83 mg/g, 활성화 에너지는 각각 2,169, 1,534 J/mol 이었다.

• 대한화학회지
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• 제15권2호
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• pp.45-48
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• 1971

The various eluents have been used for the separations of alkaline earth metals by elutions through cation exchange resin column by many investigators. We find, the mixed solution of 1M HAc and 1M NaAc (pH 4.75) is the best eluent for this purpose, becouse the one step elution through 7cm Dowex 50w${\times}$8(100~200mesh) resin column with this eluent, gives the quantitative separation. When 2M NaAc is used as a eluent Sr(II) and Ba(II) is separated easily without any contamination of Mg(II) andCa(II). The Ca-Pb alloy which is composed of Cu, Ca, Sr, Ba and abundance of Pb metal is separated quantitatively into its components by the two step elution with 0.3M HAc + 0.3M NaAc(PH 4.75) and 0.5M HAc + 0.5M NaAc(PH 4.75) as eluents through 10cm resin column.

• 대한화학회지
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• 제15권2호
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• pp.49-54
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• 1971

It is shown that the impurities of Cu(II), Pb(II), Zn(II) and Ag(I) in Bismuth metal and the components of Pb(II), Zn(II) and Sn(IV) in Bismuth alloy are separated into their components from each other by elutions through $3.14cm^2{\times}10cm$ cation exchange resin, $Dowex\;50w\;{\times}\;8$ (100~200 mesh), column with the mixed solutions of HAc and NaAc as the eluents. The elution curve of Fe(III) has a long tailing and is not separated quantitatively from Bi(III). The eluents used for this separation are as follows; 1M HAc + 0.1M NaAc (pH 3.36) for Fe(III) and Bi (III). 0.3M HAc + 0.3M NaAc (pH 4.70) for Cu(II), Pb(II) and Zn(II). 0.5M HAc + 0.5M NaAc (pH4.70) for Ag(I) and Sn(IV). The analysis of cations eluted are carried out by spectrophotometry and EDTA titrimetry. Their recoveries are more than 99%.

• 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.

• Bulletin of the Korean Chemical Society
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• 제27권5호
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• pp.694-698
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• 2006

A method has been described for the chemical speciation, preconcentration and determination of Cr(III) and Cr(VI) species in filtered tannery waste waters by flame atomic absorption spectrometry using ion-exchange resins. Amberlite IR-120($H^+$) strongly acidic cation exchanger and Amberlite IRA-410($CI ^-$) strongly basic anion exchanger resins were used for the separation and preconcentration of Cr(III) and Cr(VI) species, respectively. Optimum condition for preconcentration and speciation was obtained by testing pH of sample and eluent, flow rates of sample and eluent, amount of resins, volume of sample and eluents, and effect of foreign ions. The recommended method has been successfully applied for the preconcentration and determination of chromium species in the dissolved phase of waste water samples collected from a tannery waste water treatment plant in Kayseri, Turkey. The detection limits achieved were 0.73 $\mu$g/L for Cr(III) and 0.81 $\mu$g/L for Cr(VI). Recovery studies showed 99% for Cr(III) and 98% for Cr(VI), for samples spiked with single species.

• 대한화학회지
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• 제6권2호
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• pp.117-121
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• 1962

The waters throughout Taegu area for 87 points were analysed and according to the analytical data, following unfavorable characteristics for industrial uses were given: (1)Shows strong hardness, (2)Has high ratio of ignition residue to evaporation residue, (3) pH value is over 7, (4) Contains considerable quntities of iron.And then investigated the exchange rate and regeneration level of iron ion using cation exchange resin, Lewatit KS.When the hard water containing 2.2 ppm of iron with 18.4 ppm of calcium and 6.2 ppm of magnesium was passed through the ion exchange resin under $3cc/cm^2/min$ in exhaustant flow rate, exchange rate of iron reached to 42% after 300 hours flow. The exchange efficiency shows abrupt decreasing in initial stage of flow up to 100 hours flow. The exchanger which contains iron was regenerated with 10% sodium hydroxide aqua solution under SV (space velocity) 4. By this method, 57% of iron was eliminated from exchanger while calcium and magnesium are removed as much as 85% and 87% respectively.

• 한국작물학회지
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• 제59권3호
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• pp.252-262
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• 2014

혈당 강하를 목적으로 선발된 수수계통의 종자 유래 펩타이드의 양적, 질적 형질을 특성화하고 혈당 강하 수수에서 특이적으로 발현 펩타이드를 선발하기 위하여, 혈당 강하수수 7계통과 비 혈당 강하 수수 5계통에 대한 종자 펩타이드 프로파일링을 SELDI-TOF MS 기법을 활용하여 분석하였다. 1. 분자량의 범위가 2~20 kDa에서 검출된 수수 12계통 종자의 펩타이드는 CM10 (weak cation exchanger)에서 104개와 Q10 (strong anion exchanger)에서 95개였으며, 펩타이드 양적발현에서 12계통 간 유의성(p < 0.01)을 보인 펩타이드는 CM10에서 99개와 Q10에서 93개였다. 2. 12계통 간 양적 발현에 유의적(p < 0.01) 펩타이드를 이용한 heat map 분석에서 수수 각 계통 종자의 고유한 펩타이드 프로파일과 특이적으로 발현하는 펩타이드를 제시하고 있다. 3. 수수 12계통간의 근연거리를 이용한 군집분석에서 혈당 강하 수수 7계통과 비 혈당 강하 수수 5계통이 서로 다른 2개의 군집을 형성하였다. 4. 혈당 강하 계통에서 유의성(p < 0.00001)이 있게 발현되는 펩타이드를 29개 선정하였으며, 이중에서 혈당강하 계통에서만 공통적으로 높게 발현된 10개의 펩타이드(분자량이 2231.6, 2845.4, 2907.9, 3063.5, 3132.6, 3520.8, 4078.8, 5066.2, 5296.5, 5375.5 Da)를 선발하였다.

• 한국지반공학회:학술대회논문집
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• 한국지반공학회 2008년도 추계 학술발표회
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• pp.1475-1486
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• 2008

Bentonite-based grouting has been popularly used to seal a borehole installed for a closed-loop vertical ground heat exchanger in a geothermal heat pump system (GHP) because its high swelling potential. However, if the bentonite-based grouting is conducted in coastal areas, the salinity of groundwater changes in the mineral fabric of bentontie. In order words, an increase of cation concentration in groundwater leads to a reduction in the diffuse double-layer thickness in the bentonite mineral structure, and thus the volume of bentointe-based grouts will decrease proportional to the salinity of groundwater. In this paper, the effect of salinity (i.e., NaCl 0.5M, 0.25M, and 0.1M) on the change of swelling potential for bentonite-based grouts has been quantitatively evaluated for seven bentonite grouts from different product sources. In addition, in case of using addictives such as a silica sand to increase the thermal conductivity of bentonite-based grouts, the possibility of particle segregation has been studied considering the viscosity of grouts and salinity of groundwater.

• 한국산업융합학회 논문집
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• 제19권4호
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• pp.198-205
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• 2016

For the study on the ion exchange of nickel hexacyanoferrate(NiHCNFe) electrode with the several cations, the film of hexacyanoferrate was prepared on the bare nickel surface by the electrochemical and chemical methods in the solution composed with 5mM K3Fe(CN)6 and 100mM KNO3. To compare the capability of the ion exchange of NiHCNFe film electrode, the repeated cyclic voltammograms were measured in the 0.5M cation nitrate solutions at $25^{\circ}C$ and pH7. It was found that the capacity of the electrochemically derivatized NiHCNFe reduced in the rate of 0.5~0.7%/cycle and was nearly exhausted at the 150th potential cycle. Better result was obtained from that the capacity loss of the chemically assembled NiHCNFe was less than 0.02%/cycle for 5,000cycles. Furthermore, the residual capacity was more than 30% at the 5,000th cycle.