• 전기화학회지
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• 제1권1호
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• pp.28-32
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• 1998

1M LiPF_6/EC:DME(1:1) 전해질 용액에서 시간-전위차법, 순환 전압-전류법, 시간-전류법 , 그리고 임피던스법을 이용하여 리튬 이온 전지의 충방전 용량을 조사하였고 초기 충전과정에서 용매 분해로 형성된 필름의 영향을 알아보았다. 충 방전 결과에 따르면, 1 M $LiPF_6/EC:DME$를 이용한 반쪽전지의 초기 비가역 용량은 상당히 크게 나타났다 이러한 비가역 용량은 대부분 용매 분해에 의한 것으로 해석되었으며, 용매 분해로 인하여 MPCF전극 표면에 필름이 형성되었다. 초기 충전과정에서 형성된 필름은 방전과정에서 산화되지 않았으며 2번째 충전부터 용매 분해는 더 이상 관찰되지 않았다. 또한 초기 충전과정에서 EC:DME용매속의 Li이 MPCF층 속으로 삽입될 때 용매와 함께 삽입됨을 알 수 있었다. 이러한 삽입이 진행될 때 MPCF표면의 입자들이 박리되고, 박리된 입자들과 용매 분해 생성물들이 서로 섞여 필름을 형성하므로써 필름의 저항은 크게 나타났다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2001년도 추계학술대회 논문집 Vol.14 No.1
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• pp.545-549
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• 2001

We have produced electrolyte solution out of 1.15M $LiPF_6$ EC/EMC/DEC/PC(30/55/10/5 by vol%) as a reference, and at the same time, performed basic physical property test using a single solvent of 1.15M $LiPF_6$ DEC, DMC, EMC and a 2 component electrolyte solution of 1.15M $LiPF_6$ EC/DEC(1/2 by vol%) and PC/DEC(1/2 by vol%). Cyclic Voltammetry Analysis showed that, compared to existing carbonate organic solvent, the addition of DEC,DMC and EMC brought the de-decomposition peak of salt anion of $PF_6$ and the solvent at lower oxidization potential of 2.3V, 0.7V and 2.1V(vs. $Li/Li^+$). In addition, a kinetics current peak, in which intercalation of Lt is proceeded at 750mV, 450mV(vs. $Li/Li^+$), was confirmed. These findings suggest that the DEC solvent decomposition occurred at an electric potential lower than that of oxidization of existing carbonate organic solvent. Through the impedance analysis, we checked electric charge transfer resistance($R_{ct}$) according to the electric potential of $Li^+$ intercalation at 750mV(vs. $Li/Li^+$), which was the same as the resistance ($R_f$) and cyclic voltammetry of SEI film that was formed at Reference. By doing so, we found that the significant decrease of polarization resistance($R_p$) when Reference was played a part in the formation of compact SEI layer at the initial decomposition reaction.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2001년도 추계학술대회 논문집
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• pp.545-549
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• 2001

We have produced electrolyte solution out of 1.15M LiPF$\sub$6/ EC/EMC/DEC/PC(30/55/10/5 by vol%) as a reference, and at the same time, performed basic physical property test using a single solvent of 1.15M LiPF$\sub$6/DEC, DMC, EMC and a 2 component electrolyte solution of 1.15M LiPF$\sub$6/ EC/DEC(1/2 by vo%%) and PC/DEC(1/2 by vol%). Cyclic Voltammetry Analysis showed that, compared to existing carbonate organic solvent, the addition of DEC, DMC and EMC brought the de-decomposition peak of salt anion of PF$\sub$6/$\^$-/ and the solvent at lower oxidization potential of 2.3V, 0.7V and 2.1V(vs. Li/Li$\^$+/\`). In addition, a kinetics current peak, in which intercalation of Li$\^$+/ is proceeded at 750mv, 450mv(vs. Li/Li$\^$+/), was confirmed. These findings suggest that the DEC solvent decomposition occurred at an electric potential lower than that of oxidization of existing carbonate organic solvent. Through the impedance analysis, we checked electric charge transfer resistance(R$\sub$ct/) according to the electric potential of Li$\^$+/ intercalation at 750mv(vs. Li/Li$\^$+/), which was the same as the resistance (R$\sub$f/) and cyclic voltammetry of SEI film that was formed at Reference. By doing so, we found that the significant decrease of polarization resistance(R$\sub$p/) when Reference was played a part in the formation of compact SEI layer at the initial decomposition reaction.

• Bulletin of the Korean Chemical Society
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• 제24권7호
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• pp.967-970
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• 2003

A new modified singular value decomposition method, piecewise polynomial truncated SVD (PPTSVD), which was originally developed to identify discontinuity of the earth's radial density function, has been used for large solvent peak suppression and noise elimination in nuclear magnetic resonance (NMR) signal processing. PPTSVD consists of two algorithms of truncated SVD (TSVD) and L₁ problems. In TSVD, some unwanted large solvent peaks and noise are suppressed with a certain soft threshold value, whereas signal and noise in raw data are resolved and eliminated in L₁ problems. These two algorithms were systematically programmed to produce high quality of NMR spectra, including a better solvent peak suppression with good spectral line shapes and better noise suppression with a higher signal to noise ratio value up to 27% spectral enhancement, which is applicable to multidimensional NMR data processing.

• 멤브레인
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• 제7권2호
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• pp.49-56
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• 1997

In order to understand the formation of polymeric membranes or microcellular foams, phase separation phenomena in polymer solutions should be understood. The present review examines the progress made in the understanding of these phenomena, with emphasis on selected polymer-solvent systems. In the case of polymer-solvent systems, coarsening is of particular importance as it may come to dominate or overshadow spinodal decomposition effects within the first minute or few minutes of phase separation. In this article, some of the most important theoretical models of late stage of phase separation are reviewed, and recent experimental studies on coarsening in polymer-solvent systems are studied.

• 약학회지
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• 제28권6호
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• pp.299-303
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• 1984

In order to eluciate the effect of humidity and organic solvent on the decomposition of carbamide peroxide, the kinetic study was carried out. The carbamide peroxide was prepared from urea and 30%-hydrogen peroxide. The accelerated stability analysis for carbamide peroxide crystal in various relative humidity, and for 10%-carbamide peroxide solution of organic solvents were investigated. Both humidity and temperature were important factors influencing the decomposition rate of carbamide peroxide crystal. The higher the humidity and temperature, the greater was the reaction rate. The breakdown rate of crystal was observed as an apparent zero-order, and was faster than the rate of decomposition in dilute propylene glycol, glycerine or sorbitol solutioos which were measured as an apparent first-order reaction. The more dilute to 10% the organic solvents of 10%-carbamide peroxide, the slower was breakdown rate. It is, therefore, useful in the aspects of stability and economics to substitute solvent of carbamide peroxide topical solution (USP XXI) with 10%-propylene glycol or glycerine instead of anhydrous glycerine.

• Bulletin of the Korean Chemical Society
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• 제24권7호
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• pp.971-974
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• 2003

By utilizing singular value decomposition (SVD) and shift averaged Harr wavelet transform (WT) with a set of Daubechies wavelet coefficients (1/2, -1/2), a method that can simultaneously eliminate an unwanted large solvent peak and noise peaks from NMR data has been developed. Noise elimination was accomplished by shift-averaging the time domain NMR data after a large solvent peak was suppressed by SVD. The algorithms took advantage of the WT, giving excellent results for the noise elimination in the Gaussian type NMR spectral lines of NMR data pretreated with SVD, providing superb results in the adjustment of phase and magnitude of the spectrum. SVD and shift averaged Haar wavelet methods were quantitatively evaluated in terms of threshold values and signal to noise (S/N) ratio values.

• Bulletin of the Korean Chemical Society
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• 제22권2호
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• pp.189-193
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• 2001

The irreversible capacities caused by the reduction of solvent on the surface of a negative electrode (KMFC:Kawasaki Mesophase Fine Carbon) were examined during the initial cycle in ethylene carbonate (EC)-diethyl carbonate (DEC) electrolyte solut ions at various concentrations of LiPF6. Chronopotentiograms, linear sweep voltammograms, and impedance spectra clearly showed differences in irreversible capacity and that those differences are related to the concentration of electrolyte during the initial charge. These differences were caused by the amount of solvent decomposition as a function of the concentration of LiPF6 electrolytic salt. The data are discussed with reference to the concentration of electrolytic salt and the properties of passivation film formed by solvent decomposition.

• 공업화학
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• 제26권2호
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• pp.145-153
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• 2015

Solvent/anti-solvent법으로 제조된 $Cr_2O_3$/과염소산암모늄 에너지 복합체의 X선 회절 분석 결과 $Cr_2O_3$이 내포된 과염소산암모늄 입자는 순수한 과염소산암모늄과 동일한 결정 구조로 확인되었으며 주사전자현미경 사진으로부터 측정된 입방체 형상 결정의 평균입도는 약 $2.5{\mu}m$이었다. 복합체의 열중량 분석으로부터 $Cr_2O_3$에 의해 과염소산암모늄의 고온 분해 영역 분해 온도가 낮아짐을 알 수 있었고, 복합체 분해 반응의 활성화 에너지는 Starlink 방법에 의해 계산되었다. 이와 같은 활성화 에너지의 변화로 인하여, 과염소산암모늄의 분해 반응 메카니즘은 전환율 약 0.25까지는 주로 핵생성에 의한 다공성 구조가 생성되면서 분해되는 것으로 보이며, 전환율 0.3 이상에서는 과염소산암모늄의 격렬한 분해 반응이 승화보다 우선하는 것으로 보인다.

• Bulletin of the Korean Chemical Society
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• 제33권10호
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• pp.3196-3202
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• 2012

Post-synthesis is used to synthesize organic hybrid inorganic mesoporous sieves. In this method, the activity and structure of the base sieve are crucial to obtain the definable hybrid materials. The chemical and physical properties of the base can be largely changed either by the final step of its synthesizing processes, by template removal which is accomplished with the oxidative thermal decomposition (burning) method or by solvent extraction method. In this paper we compared two methods for the post-synthesis of organic hybrid MCM-48. When the template was extracted with HCl/alcohol mixture, the final product showed larger pore size, larger pore volume and better crystallinity compared to the case of the thermal decomposition. The reactivity of the surface silanol group of template free MCM-48 was also checked with an alkylsilylation reagent $CH_2=CHSi(OC_2H_5)_3$. Raman and $^{29}Si$ NMR spectra of MCM-48 in the test reaction indicated that more of the organic group was grafted to the surface of the sample after the template was removed with the solvent extraction method. Direct synthesis of vinyl-MCM-48 was also investigated and its characteristics were compared with the case of post-synthesis. From the results, it was suggested that the structure and chemical reactivity can be maintained in the solvent extraction method and that organic grafting after the solvent extraction can be a good candidate to synthesize a definable hybrid porous material.