• Journal of the Korean Chemical Society
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• v.19 no.5
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• pp.317-324
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• 1975

The adsorptions of gaseous $H_2O\;and\;D_2O\;on\;Na^+-,\;Ca^{2+}-,\;and\;Al^{3+}$ montmorillonites at various temperatures were undertaken. Break down of ir hydroxyl stretching bands into four Gaussian components was made by means of manual technique. Resonance theory of water to form silanol hydroxyl group was supported by $3625cm^{-1}$ band for OH and $2680cm^{-1}$ band for OD which depend on amounts of water adsorbed. The broad bands at about $3400 cm^{-1}\;and\;2475cm^{-1}$ were assigned to stretching band of silanol OH hydrogen bonded to adsorbed water. The prominent $3230 cm^{-1}$ band together with component around $2345 cm^{-1}$ were attributed to adsorbed $H_2O\;and\;D_2O$ respectively. The chemical nature of the hydrogen bonding between adsorbed water and neighboring surface OH was explained adequately in terms of electrostatic interaction.

• Journal of the Korean Chemical Society
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• v.31 no.1
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• pp.3-13
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• 1987

Infrared absorption spectra of alkyl alcohols in the OH stretching region were obtained from varying the concentrations of alcohols in $CCl_4$. The OH stretching bands were broadened and shifted to lower frequencies due to the hydrogen-bond formation. Three bands were obtained from the breakdown of these bands by the simplex method. Each band was assigned to various types of hydrogen-bonded OH groups. The electronic structures and interaction energies of dimeric and trimeric alcohols were calculated by semi-empirical MO(CNDO/2, INDO) methods. These results were in good agreement with those of deconvoluted ir spectra. The EDA(electron donor-acceptor) effect of alkyl group on hydrogen-bond formation was in the decreasing order of butyl > propyl > ethyl > methyl group. On the other hand, the experimental results were in the order : propyl > ethyl > butyl > methyl group. This seemed to be ascribed to the bulkiness of butyl alcohol.

• Proceedings of the Korean Institute of Resources Recycling Conference
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• 2005.10a
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• pp.173-177
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• 2005

리튬이온 2차전지(Lithium ion battery, LIB)는 기존에 사용되던 전지에 비해 에너지 밀도가 높고 충방전 사이클이 우수하다. 이 때문에 휴대전화와 노트북 등에 수요가 급속하게 증가하고 있으며 1995년 LIB의 생산량은 4천만 개에서 2004년에는 약 8억 개로 20배 이상 증가하였다. 이에 따라 폐LIB도 급속하게 증가하게 되어 전국적인 재활용 시스템의 확보가 필요한 실정이다. 본 연구에서는 폐LIB에 함유되어 있는 유가금속 중에서 리튬코발트옥사이드(이하 $LiCoO_2$)를 회수하기 위하여 분쇄기(orient vertical cutting mill)와 진동 Screen을 사용하여 유기분리막, 금속류(Aluminium foil, Copper foil, case 등) 그리고 전극물질(lithium cobalt oxide와 graphite 등의 혼합 분말)로 분리하였다. 전극물질에서 $LiCoO_2$와 graphite 분리를 위한 전처리 단계로서 $500^{\circ}C$ 정도의 열처리를 하여 $LiCoO_2$의 표면 성질을 변화시켜 부유선별에 의해 $LiCoO_2$와 graphite의 분리가 가능하도록 하였다. 부유선별 실험 결과 93% 이상의 순도를 가지는 $LiCoO_2$를 92% 이상 회수할 수 있었다.

• Korean Journal of Materials Research
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• v.9 no.7
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• pp.670-674
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• 1999

Accurate measurements of elastic constants are important from the view points of both science and engineering. The measurement can be viewed from scientific principle as a service tools for analyzing and improving the understanding of the nature of bondings between atoms and between ions. Also, from engineering perspective it would became an important factor to be definitely considered for the design of machinery equipments. In this investigation, two dynamic experimental methods of vibrations (acoustic method and Impulse technique method) are utilized and the results from the both methods are compared to obtain elastic constants data with a high degree of accuracy. The resonance frequencies obtained from the two methods are applied to both Euler and Timoshenko beam equations respectively, to determine the sources for possible differences.

• Proceedings of the Korean Vacuum Society Conference
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• 2011.02a
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• pp.209-209
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• 2011

플라즈마 공정에 있어 챔버 및 웨이퍼의 표면 상태변화는 공정 결과에 큰 영향을 끼치게 된다. 챔버 표면에 대한 연구는 많이 진행되어 있지만 대부분의 연구가 챔버 표면에서 일어나는 화학적 반응에 초점을 맞추고 있다. 본 연구에서는 플라즈마 상태 변화에 따른 챔버 표면물질의 전기적 특성 변화를 관찰하였다. 프로브 표면에 Al2O3로 코팅을 하고 플라즈마에 삽입 후 AC 하모닉법을 이용하여 실시간으로 표면의 축전용량을 측정하였다. 그 결과 표면의 축전용량은 플라즈마에 인가한 전력과 표면이 플라즈마에 노출된 시간에 따라 변하는 것이 관찰되었다. 플라즈마에 인가된 전력이 증가되면 처음에는 급격이 축전용량이 증가하였고, 그 후 시간이 지날수록 천천히 수렴되었다. 유전물질의 축전용량은 그 물질의 온도와 연관이 있다. 실험 결과로 미루어 보았을 때, 플라즈마에서의 표면의 축전용량의 변화는 플라즈마로부터 표면으로의 열전달에 의한 표면의 온도 변화에 의한 것으로 이해할 수 있다. 특히, 쉬스에서 가속되는 이온의 포격에 의해 표면 격자가 크게 진동하면서서 일반적인 온도 변화에 의한 축전용량의 변화보다 더 큰 변화가 일어난 것으로 추정된다. 공정에 사용되는 많은 챔버의 표면이나 전극의 표면은 유전체로 코팅되어 있다. 이 유전체의 특성이 온도에 의해 변하게 되면 챔버의 전기적인 특성이 변하게 되어 임피던스 매칭 조건에 변화를 가져온다. 그 결과 플라즈마의 특성도 바뀌게 되어 공정 결과에 영향을 미치게 된다. 그러므로 챔버 표면의 유전특성을 관찰하고 제어하는 것이 플라즈마의 특성을 유지시키는데 중요하다고 할 수 있다.

• Journal of the Korean Chemical Society
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• v.39 no.8
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• pp.611-616
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• 1995

Oxovanadium(IV) complexes with salicylaldoxime, o-vanilline oxime, 2-hydroxy-4-methoxybenzaldoxime, 2-hydroxy-5-methoxybenzaldoxime and 2-hydroxy-5-nitrobenzaldoxime were synthesized. The complexes have been characterized by elemental analysis, electric conductivity measurement, infrared spectrometry, electronic spectrometry, mass spectrometry, and thermal analysis. The results of elemental analysis were well coincided with the theoretical values. The values of molar conductance of the complexes in DMF implicated that the complexes were non-electrolyte. The characteristic stretching frequency of V=O appeared strong band in the range of $980{\pm}20\;cm^{-1}.$ All the complexes showed two d-d transition in visible spectra and two charge transfer transitions in ultraviolet spectra. Results of mass spectrometry of $VO(sal)_2\;and\;VO(van)_2$ indicated two peaks corresponding to vanadium containing ion(I) of 1 : 2(metal to ligand) chelate and a fragment ion(II) of 1 : 1 chelate due to loss of ligand radical from ion(I). The thermal analysis showed the endothermic peak due to the thermal decomposition.

• Composites Research
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• v.29 no.6
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• pp.401-407
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• 2016

IPMC is composed of thin ion conductive polymer film sandwiched between metallic electrodes plated on both surfaces. Ionic Polymer-Metal Composite (IPMC) generates voltages when bent by mechanical stimuli. IPMC has a potential for the variety of energy harvesting applications due to its soft and hydrophilic characteristics. However, the large-scale implementation is necessary to increase the output power. In this paper, the scale-up of surface area effect on voltage generation characteristics of IPMC was investigated using IPMC samples with different surface areas. Also, a circuit model simulating both the output voltage and its offset variations was designed for estimating the voltages from IPMC samples. The proposed model simulated the output voltages with offsets well corresponding to various frequencies of input bending motion. However, some samples showed that the increase of error between real and simulated voltages with time due to the nonlinear characteristic of offset variations.

• Journal of the Korean Magnetics Society
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• v.10 no.2
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• pp.81-85
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• 2000

Crystallographic and magnetic properties of the Mn-doped orthoferrite LaFe$_{1-x}$Mn$_{x}$ O$_3$(0.0$\leq$x$\leq$O.4) system have been investigated by means of x-ray diffractometry, M ssbauer spectroscopy, vibrating sample magnetometer and super-conducting quantum interference device. The structure of the system was found to be orthorhombic distorted perovskite structure. At room temperature, the M ssbauer spectra for x=0.0 consists of one Zeeman sextets from Fe$^{3+}$ ions at octahedral sites. The M ssbauer spectra of two Zeeman sextets (x$\leq$0.1) change one Zeeman sextets and a paramagnetic doublet (x=0.4). The saturation magnetization increases but the coercivity decreases with increasing x in LaFe$_{1-x}$Mn$_{x}$ O$_3$.

• Membrane Journal
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• v.20 no.3
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• pp.203-209
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• 2010

Amphiphilic graft copolymers based on poly(epichlorohydrine) (PECH) were synthesized using atom transfer radical polymerization (ATRP). Successful graft polymerization of poly(methyl methacrylate)(PMMA) and poly(butyl methacrylate) (PBMA) from PECH was confirmed by nuclear magnetic resonance ($^1H$ NMR) and FT-IR spectroscopy. Upon the introduction of KI or LiI to the graft copolymers, the ether stretching bands were shifted to a lower wavenumber due to coordinative interactions. Ionic conductivities of PECH-g-PBMA complexes were always higher than those of PECH-g-PMMA complexes, resulting from higher mobility of rubbery PBMA chains. The maximum ionic conductivity of $2.7{\times}10^{-5}\;S/cm$ was obtained at 10 wt% of KI for PECH-g-PBMA electrolytes.

• Journal of the Korean Magnetics Society
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• v.9 no.1
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• pp.1-6
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• 1999

The crystallographic and magnetic properties of the ferrimagnetic $CoFe_{1.9}Ga_{0.1}O_4$ have been studied by X-ray, M$\"{o}$ssbauer measurements. The crystal structure is found to be inverse spinel structure with the lattice constant $a_0=8.386{\pm}0.005{\AA}$. M$\"{o}$ssbauer spectra of $CoFe_{1.9}Ga_{0.1}O_4$ have been taken at various temperatures ranging from 13 to 840 K. The isomer shifts indicate that the valence states of the Fe ions for tetrahedral (A) and octahedral (B) sites have ferric character. Debye temperatures for the A and B sites are found to be 882$\pm$5 K and 209$\pm$5 K, respectively. Atomic migration form the A to the B sites starts near 350 K and increases rapidly with increasing temperature to such a degree that 73% of the ferric ions at the A sites have moved over to the B sites by 700 K. by 700 K.