• 자원리싸이클링
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• 제18권3호
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• pp.62-68
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• 2009

마그네슘 용융염 전해시 적정 조업조건을 확립하고자 자체 설계 제작한 150A급 mono-polar형 전해조를 사용하여 24시간 연속 전해 조업을 수행하였다. $MgCl_2$ 25%, NaCl 55%, $CaCl_2$ 19%, $CaF_2$ 1%의 전해욕 조성으로 전해온도 $720{\sim}740^{\circ}C$, 전해전압 7V, 음극 전류 밀도 $0.7-0.75A/cm^2$, 전극 간격 6cm의 운전조건에서 24시간 연속 조업을 수행하였으며, 전해 전압 및 전류 변화, 전해 욕 조성 변화, 전류 효율 등을 조사하였다. 시험결과 제작한 전해셀의 조업성이 양호하였으며, 순도 99% 이상의 금속 마그네슘을 회수하였고 전류효율 89%를 달성할 수 있었다. 본 연구를 통하여 마그네슘 용융염 전해장치 제작에 필요한 기초자료를 축적할 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제23권2호
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• pp.229-240
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• 2002

Quantum mechanical calculation is performed for the $O(^1D)$ + HCl ${\rightarrow}$OH + Cl reaction using Reactive Infinite Order Sudden Approximation. Shifting approximation is also employed for the l ${\neq}$ 0 partial wave contributions. Various dynamical quantities are calculated and compared with available experimental results and quasiclassical trajectory results. Vibrational distributions agree well with experimental results i.e. product states mostly populated at $v_f$ = 3, 4. Our results also show small peak at $v_f$ = 0, which indicates bimodal vibrational distribution. The results show two significant broad peaks in ${\gamma}_i$ dependence of the cross section, one is at ${\gamma}_i$ = $15^{\circ}-35^{\circ}$ and the another is at ${\gamma}_i$= $55^{\circ}-75^{\circ}$ which can be explained as steric effects. At smaller gi, the distribution is peaked only at higher state ($v_f$ = 3, 4) while at the larger gi, both lower state ($v_f$ = 0) and higher state ($v_f$ = 3, 4) are significantly populated. Such two competing contributions (smaller and larger ${\gamma}_i$) result in the bimodal distribution. From these points we suggest two mechanisms underlying in current reaction system: one is that reaction occurs in a direct way, while the another is that reaction occurs in a indirect way.

• 대한화학회지
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• 제38권4호
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• pp.283-287
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• 1994

비치오놀 설폭사이드, $C_{12}H_6Cl_4O_3S$의 결정구조를 흑연으로 단색화된 $Mo-K\alpha방사선을$ 이용하는 CAD-4 회절기를 사용하여 수집한 2295개의 독립된 회절반점을 이용하여 해석하였다. 결정계는 단사정계이며, 공간군은 P2$_1$/n이고, 격자상수는 a = 12.448(4), b = 9.740(1), c = $11.815(2)\AA$, $\beta$ = $100.06^{\circ}$, $\mu$ = 9.02 $cm^{-1}$, Dm = 1.76 g/$cm^3$, Dc = 1.75 g/$cm^3$, F(000) = 744, and Z = 4이다. 구조는 직접법으로 해석하였으며, 최소자승법으로 정밀화하여 최종 신뢰도 R=0.037인 모형을 구하였다. 분자의 전체적인 형태는 비치오놀의 경우와 비교하여 2개의 페닐링 중 한 개와 설폭사이드기를 축으로 삼아 대략 $180^{\circ}$ 정도로 회전하였음을 알 수 있었으며, 이와 같은 구조적인 변화는 S-O(3)---H-O(1)형의 분자내 수소결합의 존재와 설폭사이드기와 다른 페닐링간의 입체장에 현상 때문이다. 두 개의 페닐링은 평면구조를 나타내며, 두 평면간의 이면각은 $99.22^{\circ}$이다. 결정구조는 O(3)---H-O(2)형 분자간 수소결합에 의해 결합되어 있다.

• Bulletin of the Korean Chemical Society
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• 제32권6호
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• pp.1997-2002
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• 2011

The nucleophilic substitution reactions of dicyclohexyl phosphinic chloride [3; $cHex_2$P(=O)Cl] with substituted anilines ($XC_6H_4NH_2$) and deuterated anilines ($XC_6H_4ND_2$) are investigated kinetically in acetonitrile at 60.0 $^{\circ}C$. The anilinolysis rate is too slow to be rationalized by the stereoelectronic effects. The rate is contrary to expectations for the electronic influence of the two ligands and exhibits exceptionally great negative deviation from the Taft's eq. The deuterium kinetic isotope effects (DKIEs) involving deuterated anilines invariably change from primary normal ($k_H/k_D$ > 1; max $k_H/k_D$ = 1.10 with X = 4-MeO) with the strongly basic anilines (X = 4-MeO, 4-Me, 3-Me) to secondary inverse ($k_H/k_D$ < 1; min $k_H/k_D$ = 0.673 with X = 3-Cl) with the weakly basic anilines (X = H, 4-F, 4-Cl, 3-Cl). A concerted $S_N2$ mechanism is proposed on the basis of both secondary inverse and primary normal DKIEs. The obtained DKIEs imply that the fraction of a frontside attack increases as the aniline becomes more basic. A hydrogen-bonded, four-center-type transition state is suggested for a frontside attack, while the trigonal bipyramidal pentacoordinate transition state is suggested for a backside attack.

• E2M - 전기 전자와 첨단 소재
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• 제9권3호
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• pp.291-297
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• 1996

The surface properties of AI(Si, Cu) alloy film after plasma etching using the chemistries of chlorinated and fluorinated gases with varying the etching time have been investigated using X-ray Photoelectron Spectroscopy. Impurities of C, Cl, F and O etc are observed on the etched AI(Si, Cu) films. After 95% etching, aluminum and silicon show metallic states and oxidized (partially chlorinated) states, copper shows Cu metallic states and Cu-Cl$_{x}$(x$_{x}$ (x$_{x}$ (1

• 동아시아식생활학회지
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• 제12권6호
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• pp.554-565
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• 2002

본 연구는 식이에 결명자 분말 첨가가 흰쥐 체내의 카드뮴 축적작용에 미치는 영향을 관찰하고자 행하였다. 실험 동물은 Sprague-Dawley계(4주령,♂) 5마리를 한 군으로 정상군(Cn) 대조군(Cs), 카드윰 첨가군(Cl), 결명자(C2, C3, C4) 분말을 각각 0.5, 1.0,1.5% 수준으로 첨가한 군으로 나누어 S주간 실험을 수행하여 성장률, 식이 효율, Cd 축적량을 분석한 결과는 다음과 같다. 1. 체중 증가 경향은 C3>C2>C4>Cn>Cs>Cl군 순이었으며, 카드뮴만을 섭취한 Cl군이 가장 낮았으며, Cl군과 C3군 사이에 1%수준에서 유의성이 인정되었다. 2. 식이 효을은 C3>C2>Cs>Cn>C4>Cl군 순이었으며, 식이 효율이 가장 낮은 Cl군보다 각각 22.87, 19.89, 18.54, 14.20, 13.17% 높은 식이 효율을 보였다. 3. 날 결명자 분말을 첨가한 군의 각 장기 즉, 뇌, 심장, 비장, 간, 폐, 고환, 신장, 대퇴부근육, 다리뼈에 축적된 카드뮴 함량은 각각 0.45$\pm$0.04～0.83$\pm$0.04, 1.68 $\pm$0.02～2.16$\pm$0.02, 3.26$\pm$0.05～4.62$\pm$0.27, 37.82$\pm$0.09～47.71 $\pm$0.73, 1.07$\pm$0.10～1.66$\pm$0.04, 1.030$\pm$0.06～l.24$\pm$0.08, 36.79$\pm$0.20～39.61 $\pm$0.53, 0.87$\pm$0.02～1.00$\pm$0.02, 0.65$\pm$0.17～l.27$\pm$0.06 $\mu$g/g 범위였다. 4. 날결명자 분말첨가군 각 조직에 축적된 카드뮴 함량이 제일 낮았던 C4를 Cl과 비교한 결과 뇌, 심장, 비장, 간, 폐, 고환, 신장, 대퇴부근육, 다리뼈에 각각 49.03, 22.56, 36.02, 35.75, 41.75, 36.20, 37.00, 22.77, 56.67 %의 감소를 보였으며, 각 장기의 함량은 뇌<다리뼈<대퇴부 근육<고환<폐<심장<비장<신장<간 순 이었다. 5. 카드뮴 총 섭취량으로 장기 및 조직의 카드뮴 평균함량에 대한 축적율은 카드뮴만 섭취한 군(Cl) 의 경우 7.14%이었으며, 결명자 분말 첨가군인 C2, C3, C4군의 경우 각각 4.91, 4.81, 4.50 %이었다. 6. 체모의 카드뮴 함량은 Cl군이 가장 높았고, 결명자 첨가군들의 카드뮴 함량은 6주째까지 모든 시험군에서 증가하는 경향을 보였으며, 6주 이후에는 감소되는 경향을 보였다. 7. 분변 중 카드뮴 함량은 C4군이 가장 높았고, 결명자 첨가군들의 카드뮴 함량은 C3군과 C4군을 제외한 나머지 군들에서 완만하게 증가하는 경향을 보였으며, 6주째에 카드뮴 함량이 감소되는 경향을 보였다가 6주 이후에 다시 카드뮴 함량이 증가하는 경향이었다.

• Bulletin of the Korean Chemical Society
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• 제10권6호
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• pp.591-595
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• 1989

The$^{13}C$ NMR shifts of a series of para-substituted 9-aryl-tricyclo$[3.3.1.0^{2,8}]$non-9-yl and 8-aryl-tetracyclo$[3.2.1.0^{2,7}.0^{4,6}]$-oct-8-yl cations were measured in $FSO_3H/SO_2ClF \;at\; -90^{\circ}C\; or\; -70^{\circ}C$ in order to examine whether the ${\rho}^{c+}$ values can be used to explain the mechanism for the stabilization of the geometrically rigid cyclopropylcarbinyl cations. Plots of the ${\Delta}{\delta}^{c+}$ shifts against ${\sigma}^{c+}$ reveal excellent linear correlation. The tricyclononyl systems yield a ${\rho}^{c+}$ value of -4.95 with a correlation coefficient r = 0.9948. The tetracyclo-octanyl systems give a ${\rho}^{c+}$ value of -6.39 with r = 0.9943. A fair parallelism exists between the results of $^{19}F$ nmr studies and the change of ${\rho}^{c+}$ values in these cations. Accordingly, the present study established that the ${\rho}^{c+}$ value can be used as a mearsure of the geometric influence for the charge delocalization in cyclopropylcarbinyl cations.

• Archives of Pharmacal Research
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• 제7권2호
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• pp.115-120
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• 1984

The crystals of bromhexine-HCl, $C_{14}$ H$_{21}$ N$_{2}$Br$_{2}$Cl, are orthohombic, space group Pca2 with a = 14.598(2)A, b=12.461(3)A, c =9 9.186(1) A and Z = 4. Intensity dat for 967 reflections (Fobs > 6.sigma.(F)) were collected on a Rigaku-Denki automatic four circle diffractometer. The structure was solved by the Patterson and Fourier methods. Refinements were carried out to the final R value of 0.082. The cyclohexane ring has a normal chair form and the benzene ring is planar. There are three independenet hydrogen bounds in the structure. One is an intermolecular hydrogen bond (N-H... Cl) and the others are intramolecular hydrogen bonds (N-H...Br, N$^{+}$-H...Cl$^{[-10]}$ ) Apart from the hydrogen bounding system the molecules are held together in the crystal by van der Waals force.e.

• 한국전기전자재료학회논문지
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• 제16권6호
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• pp.449-453
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• 2003

Ferroelectric YMnO$_3$ thin films were etched with Ar/Cl$_2$ and CF$_4$/Cl$_2$ inductively coupled plasma (ICP). The maximum etch rate of YMnO$_3$ thin film was 300 $\AA$/min at a Ar/Cl$_2$ gas mixing ratio of 2/8, a RF power of 800 W, a DE bias of 200 V, a chamber pressure of 15 mTorr, and a substrate temperature of 30 $^{\circ}C$. From the X-ray photoelectron spectroscopy (XPS) analysis, yttrium etched by chemical reactions with Cl radicals assisted by Ar ion bombardments in Ar/Cl$_2$ plasma. In CF$_4$/Cl$_2$ plasma, yttrium are remained on the etched surface of YMnO$_3$ and formed of nonvolatile YF$_{x}$ compounds manganese etched effectively by chemical reactions with Cl and F radicals. From the X-ray diffraction (XRD) analysis, the (0004) diffraction peak intensity of the YMnO$_3$ thin film etched in Ar/Cl$_2$ plasma shows lower value than that in CF$_4$/Cl$_2$ plasma. It indicates that the crystallinty of YMnO$_3$ thin film is more easily damaged by the Ar ion bombardment than the changes of stoichiometry due to nonvolatile etch by-products.s.

• 한국대기환경학회지
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• 제14권6호
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• pp.631-642
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• 1998

Fall-out particles were collected by the modified British deposit gauges at 35 sampling sites in Suwon area from January to November, 1996. Twenty chemical species (Al. Ba, Cd, Cr, K, Pb, Sb, Zn, Cu, Fe, Ni, V, F-, Cl-, NO3-, 5042-, Na+, NH4+, Mg2+, and Ca2+) were analyzed by AAS and If. The purposes of this study were to estimate qualitatively various emission sources of the fell-out particle by applying multivariate statistical techniques such as factor analysis, multiple regression analysis, and discriminant analysis. During the study, outlier sites were determined by a z-score method. Cl-, Na+, Mg2+, and SO42- were highly correlated due to their common marine related source. Wind speed was the most influential factor for the deposition fluxes of the particle itself and all the chemical species as well. When applying the factor analysis, 8 source patterns were qualitatively obtained, such as marine source, soil source, oil burning source, Cr related source, tire source, Cd related source, agriculture source, and F- related source. As a result of the multiple regression analysis, we could suggest that some chemical compounds may possibly exist in the form of CaSO4, NaN03, NaCl, MgC12, (NH4)2SO4, NaF, and CaCl2 in the fall-out particles. Finally, spatial and seasonal classification study performed by a discriminant analysis showed th.at SO42-, Ca2+, Cl-, and Fe were dominant in the group of spatial pattern; however, SO42-, Cl-, Al, and V were in the group of seasonal pattern.