• 멤브레인
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• 제12권1호
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• pp.51-53
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• 2002

Poly(vinyl alcohol) (PVA)/sulfosuccinic acid $(SSA)-H^+$ 막은 1가 이온 $Li^+, Na^+,K^ + 2$가 이온 $Mg^{2+}, Ca^{2+},Ba^{2+}, 3$가 이온 $Al^{3+}$로 치환하였다. 또한 $Li^{+}$의 경우 치환도를 화하였다. 금속이온치환의 효과를 알아보기 위하여 Diffusion cell을 이용한 메탄올투과도를 측정하였다. 메탄올투과도를 1가 이온의 경우는 'Salting-out'효과뿐 아니라 electrostatic 가교와 금속 이온의 반응성에 의존한다고 사료되었다. 또한 $Li^+$이온이 경우 치환도에 비례하여 메탄올 투과도가 감소하였는데 이는 'Salting-out'효과에 기인한다고 사료되어진다.

• 한국결정성장학회지
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• 제26권6호
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• pp.238-242
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• 2016

알칼리(토)금속이 SCR(Selective Catalytic Reduction) 촉매 비활성화에 미치는영향을 미세구조, 촉매 비표면적, 기공 부피 변화, 탈질 성능 분석을 통해 규명하였다. 신촉매를 $350^{\circ}C$에서 6시간 동안 $H_3PO_4$, $K_2CO_3$, $Na_2CO_3$, $Ca(CH_3COO)_2{\cdot}H_2O$, $C_4H_6MgO_4{\cdot}4H_2O$ 수용액을 분사 시켜, 모사 피독된 SCR 촉매를 제조하였다. 피독 촉매 표면의 미세구조는 신촉매와 거의 유사한 형태를 보이지만, 비표면적과 기공 부피 변화를 신촉매와 비교하였을 때, Na < Mg < K < Ca < P 순으로 감소하는 것으로 나타났다. 특히 Na에 의해 피독된 촉매는 비표면적은 $10.20m^2/g$, 기공부피는 $0.061cm^2/g$ 정도 감소하였다. $150{\sim}450^{\circ}C$에서 신촉매 및 피독 촉매의 탈질성능을 평가한 결과, 알칼리 금속(K, Na)에 피독된 SCR 촉매가 가장 낮은 탈질효율을 보였으며, 알칼리 토금속(Ca, Mg)에 피독된 SCR 촉매는 알칼리 금속(K, Na)에 피독된 촉매에 비해 상대적으로 높은 탈질 효율을 보였으며, 인(P)에 의해 피독된 촉매는 SCR 신촉매와 거의 유사한 탈질 성능을 나타내는 것을 확인하였다. 이러한 결과는 SCR 촉매 비표면적이나 기공 부피 감소에 따른 물리적인 비활성화가 SCR 촉매 탈질 성능에 영향을 미치는 것으로 보인다.

• 분석과학
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• 제11권4호
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• pp.248-253
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• 1998

수용액에서 poly-dibenzo-18-crown-6를 이용한 알칼리, 알칼리토금속이온 및 전이금속이온들의 흡착 및 분리특성을 조사하였다. 알칼리금속이온들과 알칼리토금속이온들의 흡착정도와 분포비의 순위는 각각 Li(I)

• 한국지하수토양환경학회지:지하수토양환경
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• 제8권3호
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• pp.23-29
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• 2003

Setschenow constants of six alkali and alkaline earth metal-based electrolytes (i.e., NaCl, KCl, CaCl$_2$, K$_2$SO$_4$, Na$_2$SO$_4$, NaClO$_4$) for three polycyclic aromatic hydrocarbons (PAHs) (i.e., naphthalene, pyrene, and perylene) were investigated to evaluate the influence of a variety of inorganic salts on the aqueous solubility of PAHs. Inorganic salts showed a wide range of K$\_$s/ values (L/mol), ranging from 0.1108 (NaClO$_4$) to 0.6680 (Na$_2$SO$_4$) for naphthalene, 0.1071 (NaClO$_4$) to 0.7355 (Na$_2$SO$_4$) for pyrene, and 0.1526 (NaClO$_4$) to 0.8136 (Na$_2$SO$_4$) for perylene. In general, the salting out effect of metal cations decreased in the order of Ca$\^$2+/>Na$\^$+/>K$\^$+/. The effect of SO$_4$$\^$2-/>Cl$\^$-/>ClO4$\^$-/ was observed for anions of inorganic salts. The K$\_$s/ values decreased in the order of perylene>pyrene>naphthalene for K$_2$SO$_4$. However, the order of decreasing salting out effect for NaCl, KCl, CaCl$_2$, and NaClO$_4$ was perylene>naphthalene>pyrene. Hydration free energy of the 1:1 and 2:1 alkali and alkaline earth metal-based inorganic salts solution was observed to have a meaningful correlation with Setschenow constants. Thermodynamic interactions between PAH molecules and salt solution can be of importance in determining the magnitude of salting out effect for PAHs at a given salt solution.

• The Korean Journal of Ecology
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• 제21권5_1호
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• pp.457.1-463
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• 1998

the research has been made for alkali and metal element concentrations in top soils and plants from the abandoned coal mine, Keumsan, Chungnam Province. Samples of the top soil and plant (Miscanthus sinensis and Pinus rigida) were collected from the mine area in which was divided into t재 regions the polluted region influenced by the coal mining and the non-polluted region. pH of the top soils was 3.16-4.33 in the polluted region. Ca, Sr and P concentrations were high in the polluted soils, and Al and Ba concentrations were high in the non-polluted soils. No differences were found in K, Na and Ti concentrations. M. sinensis was higher in the element concentrations than P. rigida. In the average concentration of the alkali and metal element, M. sinensis showed high Cs and Na in the polluted region, and high Ba, Ca, K, Sr and concentrations in the non-polluted region. P. rigida had high Cs, Na and Rb concentrations in the polluted region. M. sinensis and P. rigida were higher in the root than above-ground part in the most element, but Ca and K. Ca, K and Na concentrations within both plants had higher than those of soils.

• Bulletin of the Korean Chemical Society
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• 제16권3호
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• pp.265-269
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• 1995

Complexation of ortho-xylyl-17-crown-5 (X17C5) with alkali metal ions in acetonitrile was studied by 7Li and 23Na NMR spectroscopy. The complex formation constants of X17C5 with LiI, LiSCN, NaI, and NaSCN were determined by investigating the changes in the chemical shifts as a function of the concentration ratio of X17C5 to metal ion. It was found that X17C5 forms 1:1 complex with Li+ and Na+ ions and the log Kf's for the complexation with LiI, LiSCN, NaI, and NaSCN were determined to be 2.88, 2.43, 2.53, and 2.30, respectively. In particular, the kinetics of complexation of X17C5 with Na+ was investigated by the method of 23Na NMR lineshape analysis. Activation energies were determined from Arrhenius plot of the resultant rate constant data to be 25.4 kJ/mol for NaI and 15.1 kJ/mol for NaSCN. Other kinetic parameters were also calculated by employing the Eyring equation. The decomplexation rates measured were 1.82 × 104 M-1s-1 for NaI and 1.50 × 104 M-1s-1 for NaSCN. It is concluded that the decomplexation mechanism is predominantly a bimolecular cation exchange for both cases.

• Bulletin of the Korean Chemical Society
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• 제15권8호
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• pp.654-658
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• 1994

Rate constants have been measured spectrophotometrically for the nucleophilic substitution reactions of p-and m-nitrophenyl 2-furoates (4 and 5, respectively) with alkali metal ethoxides ($EtO^-M^+$) in absolute ethanol at 25$^{\circ}$C. The reactivity of $EtO^-M^+$ toward 4 is in the order $EtO^-K^+$ > $EtO^-Na^+$> $EtO^-Li^+$ > $EtO^-K^+$+ 18-crown-6 ether. This is further confirmed by an ion pairing treatment method. The present result indicates that (1) ion paired $EtO^-M^+$ is more reactive than dissociated $EtO^-$ ; (2) the alkali metal ions ($K^+,\;Na^+,\;Li^+$) behave as a catalyst; (3) the catalytic effect increases with increasing the size of the metal ion. A similar result has been obtained for the reaction of 5, however, the catalytic effects shown by the metal ions are more significant in the reaction of 5 than in that of 4.

• 한국지하수토양환경학회지:지하수토양환경
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• 제13권5호
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• pp.74-80
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• 2008

중금속 오염 토양(Cd, Pb)에 대한 음이온성 계면활성제, AOS(alpha olefin sulfonate), SDS(sodium dodecyl sulfate) 및 LAS(linear alkyl benzene sulfonic acid)의 중금속 추출능력을 평가하였다. 계면활성제의 pH와 탄소성분 개수가 중금속 추출율에 지대한 영향을 미치는 것으로 나타났다. LAS는 산성 pH에 의한 중금속 추출효과가 높게 나타났다. SDS는 탄소개수가 AOS에 비해 적지만 중금속 추출율이 보다 높게 나타난 것은 AOS에 비하여 SDS가 작은 크기 마이셀을 형성하기에 토양과의 접촉이 보다 원활하게 일어난 것으로 판단된다. 계면활성제에 음이온성 리간드(ligand) NaI을 첨가한 결과 중금속 추출율이 Cd의 경우 1.2-2.7배 증가하였다. 반면 Pb의 경우는 0.56-1.76배로 오히려 감소하였다. 이는 $I^-$ 이온과 Pb 사이에서 형성된 비수용성 화합물이 토양에 그대로 침전되기 때문이었다. 연속식 토양칼럼실험에서도 적은 탄소개수 및 마이셀의 크기를 가지는 SDS가 토양과의 접촉 및 용탈에 보다 효율적인 것으로 나타났다.

• 한국응용과학기술학회지
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• 제22권1호
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• pp.50-55
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• 2005

A comparison of alkali metal cation and alkaline earth cation solvent extraction was made for three additional monoionizable crown ethers and one diionizable crown ether. sym-(n-Octyldibenzo)-16-crown-5-oxyacetic acid $\underline{1}$ exhibited high efficiency and selecvity in solvent extraction of alkali metal cations with respect to that observed with alkaline earth cations. Sizes of $Na^+$ and $Ca^{2+}$ appropriately match with the cavity size of monoethyl sym-bis[4(5)-tert-butylbenzo]-16-crown-5-oxymethylphosphonic acid $\underline{3}$. As the result, $Na^+$ and $Ca^{2+}$ are the best extracted. sym-(n-Octyldibenzo)-16-crown-5-oxymethyldiphosphonic acid $\underline{4}$was found to be somewhat selective for $Na^+$ over $Li^+$ and other alkaline earth metal cations. In the complexation of alklaine earth cations by crown ether diphosphonic acid $\underline{4}$, $Ca^{2+}$ and $Sr^{2+}$ are the appropriate sizes, but lager $Ba^{2+}$ may be due to favorable formation of a sandwich type complex between the crown ether cavity and the dianion of the deprotonated crown ether phoaphonic acid moiety.

• 한국응용과학기술학회지
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• 제27권4호
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• pp.552-558
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• 2010

Zinc soap and Zn/Ba mixed metal soap were synthesized and PVC plastisol with mixed metal soap and various costabilizers were also synthesized with good structures and characterized by IR and $^1H$-NMR. The IR spectrums and $^1H$-NMR spectrums of the synthesized soaps were in very good accordance with the structures proposed by earlier workers. In using phosphite as a costabilizer, TIDP phosphite was shown to be the excellent thermal stabilization effect at the low temperature and TNPP phosphite was shown to be the excellent thermal stabilization effect at the high temperature. In case of antioxidant, it was revealed that antioxidant was not effective in the low temperature thermal stabilization effect while highly effective in the high temperature thermal stability. $NaClO_4$ solution with sorbitol solvent had the best thermal stabilization effect among $NaClO_4$ solution series at low and high temperature.