• 한국전기전자재료학회논문지
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• 제23권12호
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• pp.1002-1006
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• 2010

In this study, magnesium (Mg), zinc (Zn) and aluminium (Al) as anode electrode and the solution of NaCl dissolved with 2~20 wt% as electrolytes were used for the metal-air cell. The open circuit voltage, short circuit current and I-V characteristics upon different kinds of anode electrode and electrolyte concentration were investigated. The open circuit voltage, initially about 1.45 V, rises to 1.6 V during the first 10 minutes indicating the necessity of an induction time to activate the catalyst on the air cathode. The short circuit current increases with an increased concentration of NaCl, causes an increase in the conductivity of the electrolyte solution, but the open circuit voltage did not under undergo influence of electrolyte. From NaCl 20 wt% electrolyte, the maximum output power of the magnesium electrode materials was measured with 177mW. It is found that the power characteristics of metal-air cell could be improved by using magnesium electrode materials in the NaCl electrolyte.

• Bulletin of the Korean Chemical Society
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• 제7권5호
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• pp.334-337
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• 1986

The preparation of the metal-metal bonded complex $Cp_2ZrClFeCp(CO)_2$ has been achieved by the reaction of $Cp_2ZrCl_2$ and strong nucleophile $NaFeCp(CO)_2$. The more soluble metal-metal bonded complexes $Cp_2ZrRFeCp(CO)_2(R=CH_3,\;n-C_8H_{17}$) have also been prepared through the reaction of Cp$_{2}$ZrRCl and NaCpFe(CO)$_{2}$. The complexes were characterized by IR, Raman, $^{1}$H NMR and Mass spectra. The complete absorption (100-3800 cm$^{-1}$) spectra for the three metal-metal bonded molecules are reported and the bands of each vibration were assigned.

• Advances in Energy Research
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• 제5권1호
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• pp.13-29
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• 2017

The roles of Na, Mn, W and silica, and the synergistic effects between each metal in the $MnNa_2WO_4/SiO_2$ catalyst have been investigated for oxidative coupling of methane (OCM). The crystallisation of amorphous silica during calcination at $900^{\circ}C$ was promoted primarily by Na, but Mn and W also facilitated this process. The interaction between Na and Mn tended to increase the extent of conversion of $Mn_3O_4$ to $Mn_2O_3$. The formation of $Na_2WO_4$ was dependent on the order in which Na and W were introduced to the catalyst. The impregnation of W before Na resulted in the formation of $Na_2WO_4$, but this did not occur when the impregnation order was reversed. $MnWO_4$ formed in all cases where Mn and W were introduced into the silica support, regardless of the impregnation order; however, the formation of $MnWO_4$ was inhibited in the presence of Na. Of the prepared samples in which a single metal oxide was introduced to silica, only $Mn/SiO_2$ showed OCM activity with significant oxygen conversion, thus demonstrating the important role that Mn plays in promoting oxygen transfer in the reaction. The impregnation order of W and Na is critical for catalyst performance. The active site, which involves a combination of Na-Si-W-O, can be formed in situ when distorted $WO_4^{2-}$ interacts with silica during the crystallisation process facilitated by Na. This can only occur if the impregnation of W occurs before Na addition, or if the two components are introduced simultaneously.

• 분석과학
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• 제10권1호
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• pp.60-65
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• 1997

mono-crown ether(benzo-15-crown-5)와 benzo-15-crown-5를 포함한 bis-(crown ether)s(ethylenediamine bis(4'-formylbenzo-15-crown-5))에 의한 알칼리금속과 알칼리토금속 양이온들의 용매추출을 $25^{\circ}C$, 물-클로로포름계에서 조사하였다. mono-crown ether와 bis-(crown ether)s를 사용한 경우 알칼리금속과 알칼리토금속 양이온들에 대한 추출평형상수($K_e$)와 착물형성상수($K_c$)의 크기 순위는 각각 Ca(II)>Na(I)>Sr(II)>K(I)>Mg(II)>Rb(I)와 Sr(II)>Ca(II)>K(I)>Rb(I)>Mg(II)>Na(I) 순으로 증가하였다. 이들 크기 순위는 금속 양이온의 크기 및 전자밀도효과로서 설명할 수 있었다. 또한 mono-crown ether에 비해서 bis-(crown ether)s를 사용한 경우 금속양이온들에 대한 추출효율이 좋게 나타남을 알 수 있었다.

• Journal of the Korean Wood Science and Technology
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• 제27권1호
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• pp.18-23
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• 1999

3회축을 갖는 Na-cellulose II의 형성조건을 X선회절법을 이용하여 검토하였다. 그 결과 Na-cellulose II는 Na-cellulose I 을 거쳐서 형성되며 결정중의 알칼리농도가 Na-cellulose I 이나 III보다 높은 조건에서 형성되는 것으로 생각되었다. 2회축에서 3회축으로의 섬유주기의 급격한 변화는 알칼리 처리 후의 수분제거방법에 의해 크게 영향받는 것으로 생각되었다. 동(銅)-알칼리셀룰로오스 복합체의 결정은 팽윤상태에서 안정된 구조를 가지며 건조에 의해 결정구조가 변화되었다.

• 공업화학
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• 제5권6호
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• pp.1024-1029
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• 1994

경북 감포지역에서 산출되는 천연 제올라이트를 각기 다른 농도의 HCl과 NaOH로 화학처리한 시료와 금속양이온 교환한 시료를 제조 하였다. 이들 시료에 대한 질소의 흡착특성을 $25^{\circ}C$, 100~760 torr의 범위에서 조사하였다. 산처리한 시료의 질소 흡착량은 처리하기 전보다 감소하였으며, 알칼리 처리한 시료는 많이 증가하였다. 0.5N-HCl 처리 후 0.5N-NaOH로 연속처리한 경우 약 200% 정도 흡착량이 개선되었으나, 알칼리 처리 후 산으로 연속처리한 경우에는 오히려 감소하였다. $Na^+$, $K^+$, $Cs^+$를 이온교환한 경우 이온의 크기가 증가할수록 흡착량은 감소했으며, $Mg^{2+}$, $Ca^{2+}$, $Ba^{2+}$를 이온교환한 경우는 이온의 크기가 증가할수록 흡착량이 증가하였다.

• Bulletin of the Korean Chemical Society
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• 제26권3호
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• pp.423-427
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• 2005

The bis(2,4,4-trimethylpentyl)phosphinic acid (Cyanex-272) and sodium diethyl- dithiocarbamate (NaDDC) ligands were used to extract of metal ions ($Cd^{2+},\;Co^{2+},\;Cu^{2+},\;Pb^{2+},\;Zn^{2+}$) in supercritical $CO_2$. Experiments showed a strong synergistic effect and better extraction efficiency if the two ligands were used together. In-situ UV-visible observation indicates that NaDDC in the water/supercritical $CO_2$ started to decompose slowly. The synergistic effect seems to come from the deprotonation of the organophosphorus ligand by amines from the decomposed NaDDC. The enhancing role of amines was confirmed using the mixture of Cyanex-272 and diethylamine(DEA) in the metal extraction.

• 한국식품영양학회지
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• 제3권2호
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• pp.169-176
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• 1990

Effects of metal chelating agents and metal ions on the volatile substance of cooked oil with chicken and pork mixture meat were examined by chemical analysis and sensory test. The addition of Na-tripolyphosphate(Na-TPP) to chicken and pork mixture meat increased the amount of H2S among volatiles evolved during cooking but decreased that of volatile carbonyl compounds(VCC) This treatment enhanced meat flavor in cooked oil with chicken and pork mixture. It was recognized that the increase in Ha5 evolution was caused by the rise of pH value. On the contrary cupric ion produced a negative effect on the production of chicken and pork mixture meat flavor and this addition increased VCC and TBA value. Other metal chelating agents such as citric acid, phytic acid and EDTA, provided the same results as Na-TPP. It was supposed that these phenomena were attributable to the chelating action to metal prooxidant in mixture meat at could be concluded that a proper evolution of H2S and protection against lipid oxidation during cooking were important to produce an excellent chicken and pork mixture meat flavor.

• Korean Chemical Engineering Research
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• 제46권2호
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• pp.423-429
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• 2008

석탄을 가스터빈에 직접 사용하여 발전 효율을 높이고자 용매추출법으로 회분이 제거된 청정석탄 제조공정이 개발되고 있다. 용매추출에 의해 생산된 청정석탄에는 미량의 알카리금속이온이 들어있어서 연소시에 터빈 날개의 부식을 일으킬 수 있다. 이 연구에서는 청정석탄 제조공정의 알카리금속이온 제거를 위하여 무기이온교환제인 ${\alpha},{\beta}$-인산금속 산화물들(ZP: $Zr(HPO_4)_2$, TP: $Ti(HPO_4)_2$, ZTP: $ZrTi(HPO_4)_4$, Z1TP3: $Zr_{0.25}Ti_{0.75}(HPO_4)_4$, Z3T1P: $Zr_{0.75}Ti_{0.25}(HPO_4)_4$)과 H-Y 제올라이트를 제조하여 수용액 및 석탄이 용해된 고온의 유기용매(N-methyl-2-pyrrolidone)에서 나트륨 이온 제거 특성을 비교 분석하였다. ${\beta}$ 형태의 인산금속산화물들은 모사 수용액($Na^+$ Conc. 100 ppmw)에서 ${\alpha}$ 형태에 비해 높은 이온교환용량을 가지고 있으며 H-Y 제올라이트에 비해서도 높은 나트륨 이온 제거용량을 보여주었다. 이온교환매체가 고온의 유기용매($Na^+$ Conc. 12 ppmw in NMP)일 경우에는 H-Y 제올라이트의 나트륨이온 제거율은 $300^{\circ}C$까지 90% 이상이었으나, 그 이상의 온도에서는 50% 가량으로 급격히 감소하는 경향을 보여주었다. 그러나 ${\beta}$ 형태의 인산금속산화물들은 여러 온도조건($250{\sim}400^{\circ}C$)에서 90% 이상의 제거율을 나타내었고 강산용액을 이용한 재생 후에도 최초 실험과 유사한 나트륨 이온 제거율을 보여주었으며 그 중 가장 높은 제거율을 나타낸 $Zr_{0.75}Ti_{0.25}(HPO_4)_2$는 알카리금속이온 제거공정에 가장 적합한 무기이온교환제로 판단된다.

• Bulletin of the Korean Chemical Society
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• 제17권9호
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• pp.840-845
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• 1996

Rate constants have been measured spectrophotometrically for the reactions of p-and m-nitrophenyl 2-thiophenecarboxylate (5a and 5b, respectively) with alkali metal ethoxides (EtO-M+) in absolute ethanol at 25.0±0.1 ℃. The reactivity of EtO-M+ exhibits dependence on the size of alkali metal ions, i.e. the reactivity of EtO-M+ toward 5a decreases in the order EtO-K+ ≥ EtO-Na+ > EtO-Li+ > EtO-, while the one toward 5b does in the order EtO-Na+ ≥ EtO-K+ > EtO-Li+ > EtO-. This result indicates that ion paired EtO-M+ is more reactive than dissociated EtO-, and alkali metal ions form complexes with the substrate more strongly at the transition state than at the ground state. The catalytic effect shown by alkali metal ions appears to be less significant in the reaction of 5 than in the corresponding reaction of 4, indicating that complexation of alkali metal ions with 5 is not as strong as the one with 4.