• Bulletin of the Korean Chemical Society
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• 제23권8호
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• pp.1067-1072
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• 2002

A new polystyrene-divinylbenzene resin containing 2-(2-thiazolylazo)-5-dimethylamino-phenol (TAM) functional groups has been synthesized and its sorption behavior for nineteen metal ions, including Zr(Ⅳ),Hf(Ⅳ) and U(Ⅵ) has been investigated by batch and column methods. The chelating resin showed high sorption affinity for Zr(Ⅳ) at pH 1-5 and U(Ⅵ) at pH 4. Some parameters affecting the sorption of the metal ions have been detailed. The breakthrough and overall capacities were measured under optimized conditions. The overall capacities of Zr(Ⅳ), Th(Ⅳ) and U(Ⅵ), which showed higher than the other metal ions, were 0.90,0.84 and 0.80 mmol/g, respectively. The elution order of metal ions at pH 4 was evaluated as Zr(Ⅳ) > Th(Ⅳ) > U(Ⅵ) > Cu(Ⅱ) > Hf(Ⅳ) > W(Ⅵ) > Mo(Ⅵ) > In(Ⅲ) > Sn(Ⅳ) > Cr(Ⅲ) > V(Ⅴ) > Fe(Ⅲ). Quantitative recovery of most metal ions except Zr(Ⅳ) was achieved using 2M HNO3. Desorption and recovery of Zr(Ⅳ) was successfully performed with 2 M HClO4 and 2 M HCl.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2000년도 추계학술대회 논문집
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• pp.124-128
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• 2000

The high Tc phase disappeared and low Tc phase increased in the substitution of transition elements for Bi ions. The high Tc phase decreased in the substitution of Si and Sn for Bi ions. The high Tc phase increased in the substitution of Sb, As and P which were the same group of Bi for Bi ions. The substitution of P ions was the most effective and then the high Tc phase was formed in large quantity by replacing Bi ions with 30% of P ions.

• Bulletin of the Korean Chemical Society
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• 제21권10호
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• pp.1047-1048
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• 2000

Dye-sensitized nanocrystalline rutile $TiO_2$ solar cells were prepared, and the influence of Li+ and 1,2-dimethyl-3-hexyl imidazolium ions in the electrolyte on the photovoltaic properties was compared. The electrolyte con-taining Li+ ions produced a lower open-circuit photovoltage than the electrolyte with 1,2-dimethyl-3-hexyl im-idazolium ions, suggesting that the adsorption of Li+ ions to the rutile $TiO_2$ surface causes a shift in the band edges toward more positive potentials. At the same time, both the short-circuit photocurrent and the maximum value of the incident-photon-current conversion efficiency (IPCE) of the electrolyte containing Li+ ions were relatively higher. Data analysis suggests that presence of adsorbed Li+ ions improves via the phenomenon of band-edge movement the charge-injection efficiency by altering both the energy and number of excited state levels of the dye that participate in electron injection.

• Bulletin of the Korean Chemical Society
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• 제20권12호
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• pp.1501-1505
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• 1999

Expansion dynamics of C$^{+}$ ions ejected from 355-nm laser ablation of graphite target in vacuum has been investigated by pulsed-field time-of-flight (TOF) mass spectrometry. A strong nonlinear dependence of the amount of desorbed C$^{+}$ ions on laser fluence is interpreted by the mechanism that C$^{+}$ ions are produced directly from the graphite via conversion of the multiphoton energy into thermal energy. The temporal evolution of C$^{+}$ ions was measured by varying the delay time of the ion repelling pulse with respect to the laser irradiation, which provides significant information on the ablated plume characterization. The TOF distributions of ablated ions showed a bimodal shape and could be fitted by shifted Maxwell-Boltzmann distributions. The velocity of the fast component increases with the delay time, whereas the slow component (< 500 m/s) exhibits a constant velocity. Also studied were the effects of the laser fluence on the energetics of C$^{+}$ ions.

• 분석과학
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• 제13권6호
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• pp.699-704
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• 2000

도금폐수중의 시안이온의 전기화학적 분해 및 아연이온의 제거에 관한 연구를 백금으로 도금된 티타늄 양극과 스텐레스 음극 전극을 사용하여 수행하였다. 전기분해시간, 셀전류, 첨가제, 염화물농도등의 여러 가지 실험파라메터를 연구하여 도금폐수중의 시안화물 분해 및 수용액중의 아연이온의 효과적인 제거에 사용하였다. 셀전류와 첨가제의 종류에 따라 시안이온의 분해 및 아연이온의 제거 효율이 크게 영향을 받는 것이 발견되었다. 시안이온의 분해 및 아연이온의 제거를 위한 경제적이며 높은 효율을 나타내는 최적화된 조건은 1시간의 전기분해시간, 12A의 전류, 그리고 0.5 M NaCl 첨가제를 사용하여 확립하였다. 양극에서의 시안이온의 분해에 관한 반응메카니즘도 논의하였다.

• Bulletin of the Korean Chemical Society
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• 제23권12호
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• pp.1759-1764
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• 2002

Two crystal structures of dehydrated $Ag^+-andTl^+$-exchanged zeolite X$Ag_{27}Tl_{65-}X\;and\;Ag_{23}Tl_{69-}X$have been determined by single-crystal X-ray diffraction techniques in the cubic space group Fd3 at 21(1) $^{\circ}C(a=24.758(4)\AAa=24.947(4)$, ${\AA}respectively).$, Their structures were refined to the final error indices $R_1$=0.055 and $wR_2$=0.057 with 375 reflections, and $R_1$=0.057 and $wR_2$=0.057 with 235 reflections, respectively, for which I > $3\sigma(I).$ In the structure of $Ag_{27}Tl_{65-}X,\;27\;Ag^+$ ions were found at two crystallographic sites: 15$Ag^+$ ions at site I at the center of the hexagonal prism and the remaining 12$Ag^+$ ions at site II' in the sodalite cavity. Sixty-five $Tl^+$ ions were located at three crystallographic sites: 20$Tl^+$ ions at site II opposite single six-rings in the supercage, 18$Tl^+$ ions at site I' in the sodalite cavity opposite the D6Rs, and the remaining 27$Tl^+$ ions at site III' in the supercage. In the structure of $Ag_{23}Tl_{69-}X$, 23$Ag^+$ ions were found at two crystallographic sites: 15 at site I and 8 at site II'. Sixty-nine $Tl^+$ ions are found at four crystallographic sites: 24 at site II, 17 at stie I', and the remaining 28 at two III' sites with occupancies of 22 and 6.

• 대한화학회지
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• 제38권7호
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• pp.509-515
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• 1994

고리(12C4, 15C5, 18C6, DT18C6, DA18C6) 및 비고리$(Q_2O_5)$ 폴리에테르와 11가지의 1차 및 2차 알킬암모늄 이온과의 상호작용을 NMR 적정과 전기전도도법으로 조사하였다. 모든 알킬암모늄 이온은 크라운 에테르 및 비고리 폴리에테르와 수소결합에 의해 비교적 안정한 1:1 착물을 형성하였다. 알킬암모늄 이온과 동공의 크기가 다른 동일계열 호스트와의 상호작용의 세기는 18C6 > 15C5 > 12C4 순이었으며, 알킬암모늄 이온에 대한 호스트 주개원자의 세기는 N > O > S 순이었다. 18C6는 2차 알킬암모늄 이온에 비해 1차 알킬 암모늄 이온과 더 강한 상호작용을 하는 반면, DA18C6는 2차 알킬암모늄 이온과 더 강한 상호작용을 하였다. 또한 25$^{\circ}C$ 메탄올에서 18C6와 알킬암모늄 이온과의 착물형성에 대한 안정도 상수를 전기전도도법에 의해 구하였다. 착물의 안정도는 주로 알킬암모늄의 차수(또는 수소결합 수), 알킬기의 길이, 알킬기의 구조에 의한 입체장애 등에 의해 크게 영향을 받았다.

• 공업화학
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• 제25권3호
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• pp.307-311
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• 2014

본 연구에서는 4종류의 목재 폐기물(밤나무, 소나무, 낙엽송, 아카시아) 중에서 구리 이온 제거 능력이 뛰어난 생물흡착제로서 밤나무를 도출하였으며, 또한, 이 밤나무를 이용하여 수중에 함유된 5, 10, 20, 40 mg/L 구리 이온의 제거 효율에 대하여 고찰하였다. 5 mg/L 구리 이온 제거를 위하여, $43{\sim}63{\mu}m$ 입자 크기의 밤나무 사용이 가장 효과적임을 알 수 있었다. 밤나무 주입 농도를 증가하였을 때, 구리 제거효율이 향상되었다. 또한, 0.8 g/100 mL 밤나무가 30 min 동안 사용되었을 때, 20, 40 mg/L 구리 이온 제거효율은 각각 99, 85% 제거효율을 나타내었다. 그리고 50 mg/L 구리 이온의 제거 능력을 향상시키기 위하여, 밤나무에 1 M 아세트산나트뮴의 화학적 처리가 필요함을 알 수 있었다. 한편, 개질된 밤나무를 재활용하기 위하여 최적의 탈착제로서 93% 구리 탈착 효율을 나타낸 1 M 염산을 선정하였다. 따라서 이러한 실험 결과들은 경제적이고 실용적인 공학 자료로서 구리 제거 공정 개발에 활용될 수 있을 것이다.

• Bulletin of the Korean Chemical Society
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• 제10권3호
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• pp.234-238
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• 1989

The crystal structure of partially $Ag^+$-exchanged zeolite A, $Ag_{3.2}Na_{8.8}$-A, vacuum dehydrated at $360^{\circ}C$ and then exposed to 0.1 torr of cesium vapor for 12 hours at $250^{\circ}C$ has been determined by single-crystal X-ray diffraction techniques in the cubic space group Pm3m (a = 12.262(2)${\AA})\;at\;21(1)^{\circ}C$. The structure was refined to the final error indexes $R_1=0.068\;and\;R_2=0.072$ by using 338 reflections for which $I_o\;>\;3{\sigma}(I_o)$ and the composition of unit cell is $Ag_{3.2}Cs_{8.8}-A.\;3\;Cs^+$ ions lie on the centers of the 8-rings at sites of D4h symmetry. Two crystallographycally different 6-ring $Cs^+$ ions were found: 1.5 $Cs^+$ ions at Cs(2) are located inside of sodalite cavity and 4.3 $Cs^+$ ions at Cs(3) are located in the large cavity. The fractional occupancies observed at Cs(2) and Cs(3) indicate that the existence of at least three types of unit cells with regard to the 6-ring $Cs^+$ ions. For example, 50% of unit cells may have two $Cs^+$ ions at Cs(2) and 4 $Cs^+$ ions at Cs(3). 30% of unit cells may have one Cs+ ion at Cs(2) and 5 $Cs^+$ ions at Cs(3). The remaining 20% would have one $Cs^+$ ion at Cs(2) and 4 $Cs^+$ ions at Cs(3). On threefold axes of the unit cell two non-equivalent Ag atom positions are found in the large cavity, each containing 0.64 and 1.92 Ag atoms, respectively. A crystallographic analysis may be interpreted to indicate that 0.64 $(Ag_5)^+$ clusters are present in each large cavity. This cluster may be viewed as a tetrasilver molecule $(Ag_4)^0$(bond length, 2.84${\AA}$) stabilized by the coordination of one $Ag^+$ ion.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2012년도 제43회 하계 정기 학술대회 초록집
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• pp.166-166
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• 2012

We examined the distribution of Co ions of ferromagnetic n-type Zn(1-x)Co(x)O semiconducting films with the Co concentrations of 0.03~0.07 using x-ray absorption fine structure (XAFS) measurements at the Co and Zn K edges. Extended XAFS (EXAFS) revealed that Co ions mainly occupied the zinc sites of the films. X-ray absorption near edge structure (XANES) spectra demonstrated that the pre-edge peak of the Co K edge was substantially affected by the second neighboring Co ions at the zinc sites due to hybridizing of the Co 4p conduction electrons with the Co 3d bounded electrons. From XANES and EXAFS analysis using ab initio calculations, we found that Co ions uniformly occupied the zinc sites of the Zn (0.93) Co (0.07)O film, whereas the Co ions of the Zn (0.97) Co (0.03)O and Zn (0.95) Co (0.05)O films were substituted at localized zinc sites. The ferromagnetic properties of the Zn (0.93) Co(0.07)O film could be induced by direct interaction between the magnetic dipoles of the Co ions with a mean distance of 4.3 A or by Co 4p electron mediation.