• Economic and Environmental Geology
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• v.21 no.2
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• pp.165-169
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• 1988

Negative induced polarization (IP) responses are examined for two-dimensional structures using a modeling technique with finite difference method. Percent frequency effect is used for IP parameter because it can be efficiently computed by a perturbation method. Thin conductive, polarizable overburden causes obvious negative IP responses on IP pseudosection. This fact means that IP responses from resistive, polarizable body below the overburden can be masked solely as a function of the resistivity distribution. Resistive, non-polarizable body below the overburden, however, can be detected by the negative IP responses.

• East Asian mathematical journal
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• v.32 no.1
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• pp.61-75
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• 2016

If ${\phi}$ is a polarizable endomorphism on a projective variety, then the Weil height machine guarantees that ${\phi}$ satisfies Northcott's theorem. In this paper, we show that Northcott's theorem only holds for polarizable endomorphisms and generalize this result to arbitrary dominant endomorphisms: we introduce the height expansion and contraction coefficients which provide weak Northcott's theorem for dominant endomorphisms. We also give some applications of the height expansion and contraction coefficients.

• Bulletin of the Korean Mathematical Society
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• v.49 no.2
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• pp.307-317
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• 2012

We say (W, {${\phi}_1,\;{\ldots}\;,{\phi}_t$}) is a polarizable dynamical system of several morphisms if ${\phi}_i$ are endomorphisms on a projective variety W such that ${\otimes}{\phi}_i^*L$ is linearly equivalent to $L^{{\otimes}q}$ for some ample line bundle L on W and for some q > t. If q is a rational number, then we have the equidistribution of small points of given dynamical system because of Yuan's work [13]. As its application, we can build a polarizable dynamical system of an automorphism and its inverse on a K3 surface and can show that its periodic points are equidistributed.

• Economic and Environmental Geology
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• v.19 no.3
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• pp.219-224
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• 1986

Spectral induced polarization (IP) responses for 20-degree dipping body are obtained by both numerical and scale models. The IP responses for the dipping body vary not only with current frequencies but also with resistivity ratios between the body and the surrounding medium. If the ion concentration related to polarizable reaction is constant, the resistivity of polarizable body depends only on the current frequency. This implies that the IP responses to the resistivity ratio are qualitatively equivalent to those to the current frequency. The numerical results with wide-range resistivity ratios, therefore, can be used as standard curves for the interpretation of spectral IP data.

• Bulletin of the Korean Chemical Society
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• v.15 no.10
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• pp.860-864
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• 1994

2nd-order rate constants have been measured spectrophotometrically for the reactions of 4-nitrophenyl benzoate (1), S-4-nitrophenyl thiobenzoate (2) and 4-nitrophenyl thionbenzoate (3) with alkoxides, aryloxides and thioaryloxides in absolute ethanol at 25.0 ${\pm}0.1$${\circ}C$. The substitution of O by polarizable S in the leaving group has little affected the reactivity of 2 toward the charge localized species (eg. $EtO^-$ and $CF_3CH_2O^-$), while the effect of the similar replacement in the carbonyl group has led to a decrease in reactivity by a factor of 10. However, the reactivity of these esters toward charge delocalized aryloxides has been found to be in the order $1<3{\le}2$. The effect of replaced sulfur atom on reactivity becomes more significant for the reaction with polarizable thioaryloxides, i.e. the reactivity increases in the order $1<2{\ll}3$. The difference in reactivity for the present system is attributed to a polarizability effect.

• Bulletin of the Korean Chemical Society
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• v.11 no.6
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• pp.487-493
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• 1990

A complete potential profile of an electrical double layer is calculated from a distribution function of charged particles based upon a model where the effect of a charged electrode and the finite size of ion are explicitly included. Electrons which are distributed on the electrode surface are assumed not to penetrate the electrode/electrolyte boundary. Formation of the constant density regions and their effects on potential and the electrical double layer capacitances are studied in great detail. The distribution of surface electrons as well as the constant density regions are found to be essential in characterizing the electrical double layer. The introduction of the ion size into the prior electrical double layer model of an ideally polarizable electrode/point charged electrolyte system, shows a great improvement in its characteristics mostly at negative potential region.

• Proceedings of the Materials Research Society of Korea Conference
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• 1993.05a
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• pp.53-54
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• 1993

• Korean Journal of Materials Research
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• v.3 no.2
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• pp.185-192
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• 1993

Abstract Electrorheological effect on the dispersive system of polarizable fine powder/dielectric oil has been investigated. ER effect was explained divided into following 3 mechanisms; (1) surface conductance, (2) bulk conductance, and (3) induced polarization. Mathematical model which predicts the interactive force between two fine particles in the electrorheological fluid has been introduced based on the induced polarization mechanism. This model may provide guide to select materials for strong ER effect. The attractive force between two particles was calculated using the above model for the selected 7 materials such as ceramics, ferrites, polymers etc. From the calculation result, it was found that the ceramics and ferrites are good materials which show a strong ER effect.

• Proceeding of EDISON Challenge
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• 2016.03a
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• pp.120-125
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• 2016

용매화 된 이온들간의 상호작용은 화학을 비롯한 여러 분야에서 중요하게 다뤄지고 있다. 계산화학에 있어 다양한 용매에 용매화 된 이온들간의 상호작용은 분자동력학 시뮬레이션(MD)을 이용한 PMF 계산을 통해 많이 연구되어 왔는데, 본 그룹에서는 물을 표현할 수 있는 다양한 모델과 Salt solution 하에 Na+ 이온과 Cl- 이온 사이 상호작용을 PMF 계산을 통해 알아보았다. 첫 번째로 Polarizable water model인 Tip4p-fq를 사용한 PMF 계산 결과는 아직 진행 중에 있으며 결과적으로는 기본적으로 CHARMM water force field에서 제공해주는 Tip3p 모델 및 양자계산 방법 중 하나인 Ab initio를 이용한 결과와 비교, 분석 할 예정이다. 두 번째로 1M/2M/5M Salt solution의 서로 다른 농도를 사용하여 시뮬레이션 한 결과 1M과 2M에서는 물 속에서 시뮬레이션 한 결과와 큰 차이가 없었으나 농도가 짙은 5M 용매 내에선 $Na^+$이온과 $Cl^-$이온 사이 거리가 멀어질수록 주변 Salt에 영향을 받는 것을 확인 할 수 있었다. 결론적으로 본 연구를 진행함으로써 우리는 서로 다른 전하를 갖는 이온 사이 상호작용에 대한 이해를 더 높일 수 있었다.

• Journal of the Korean Geophysical Society
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• v.5 no.1
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• pp.9-18
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• 2002

We performed a long-term monitoring of self-potential(SP) using the Cu-CuSO₄non-polarizable electrode and copper-clad electrodes(CCE) in a test site in order to analyze the effects of surrounding environmental noises such as temperature, rainfall and soil moisture content on the electrodes. Analysis of the temperature dependence of the non-polarizable electrodes showed that is temperature coefficient was about +0.5 mV/°Fwhen its end was exposed to atmosphere while it was less than +0.5 mV/℃ when submerged into the subsurface, which reflects that there exists an 8 to 11 hour lag between temperatures at the depth of 15 cm and atmosphere. CCE was independent of atmospheric temperature in subsurface but showed temperature coefficient of 1.0 mV/℃ when exposed to atmosphere. Drifts of 1 to 2 mV recorded with the non-polarizable electrode directly related to the soil moisture content when it was buried in subsurface. Drift with CCE also showed similar trend to the soil moisture content, and 5 mV drift was recorded according to 5% of daily variation. The soil moisture content had strong effects on the measurement with CCE in rainfall since the flow potential is generated on the surface of the electrode.