• 한국광학회:학술대회논문집
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• 한국광학회 2000년도 제11회 정기총회 및 00년 동계학술발표회 논문집
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• pp.130-131
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• 2000

One of the more promising proposals for guiding and focusing neutral atoms involves dark hollow laser beams. When the frequency of the laser is detuned to the blue of resonance, the dipole force the atoms feel in the light confines them to the dark core where the atoms can be transported with minimal interaction with the light. The ability of the all-light atom guides to transport large number of ultracold atoms for long distances without physical walls leads to the possibility of a versatile tool for atom lithography, atom interferometry, atomic spectroscopy as well as for transporting and manipulating Bose-Einstein condensates. Furthermore since the atoms transported in all-light atom guides do not come into contact with matter, they can in principle be used to transport antimatter as well. The ability to vary the core size of the hollow beam makes the all-light atom guide potentially useful for focusing neutral atoms. The atoms could be focused as tight as the core size of the hollow beam at its waist. This new focusing scheme, called the atom funnel, would not show spherical and chromatic aberrations that conventional harmonic focusing suffers from. (omitted)

• 한국CDE학회논문집
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• 제20권4호
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• pp.321-327
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• 2015

In the protein database search, 3D structural shape comparison for protein screening plays a important role. Protein databases have big size and have been grown rapidly. Exhaustive search methods cannot provide a satisfactory performance. As protein is composed of a set of spheres, the similarity calculation of two set of spheres is very expensive. Thus, a reasonable filtering method could be an answer for the speedup of protein screening. In this paper, we suggest a speedup method for protein screening with atom number and bounding sphere. We also show some experimental results for the validity of our method.

• Bulletin of the Korean Chemical Society
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• 제10권2호
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• pp.161-167
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• 1989

The results of ab initio(MP2/6-31G) molecular orbital calculations of the dipole moment derivatives and gas phase IR intensities in chloromethanes are reported. The theoretical polar tensors are analyzed into the net charge, charge-flux, and overlap contributions. The charge-flux contribution was found to be dominant in the Cl atom polar tensor, while the net charge effect was the most prominent contribution for the H atom polar tensor. The Cl atom polar tensor appeared, in a good approximation, to be transferable among various chloro molecules. On the other hand, for the prediction of IR spectra of complex hydrocarbons containing chlorine atoms, some empirical adjustment of the H-atom polar tensor seemed to be made depending on the number of Cl atoms bound to the certain carbon atom.

• 컴퓨터교육학회논문지
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• 제17권1호
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• pp.107-115
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• 2014

본 논문은 다중코어의 성능을 평가하고 분석하기 위해 TILE-Gx36(Gx36) 다중코어 프로세서를 사례로 연구하였다. Gx36의 성능 평가는 비교적 최신 병렬 벤치마크인 PARSEC을 이용하였고, 성능 분석을 돕기 위한 비교 시스템으로 인텔의 Core i7 (i7)과 Atom을 사용하였다. 실험결과 2의 제곱으로 동시에 수행 가능한 스레드를 발생시켰을 때, Gx36은 i7보다 평균 2.73배 낮은 성능을 보였으며, Atom보다는 평균 1.93배 높은 성능을 보였다. Gx36은 비교 프로세서보다 상대적으로 큰 Last-Level Cache(LLC)를 갖고 있음에도 불구하고, 가장 많은 LLC miss를 발생시켰다. 이는 Gx36이 기대치 이하의 성능을 보이는 주된 이유로 판단되며, DDC가 일반적 고성능 컴퓨팅을 위한 캐시구조로 적절하지 않음을 보여준다. 다중코어 시스템의 실측을 통한 성능평가는 향후 다중코어 구조개선 및 올바른 방향 설정을 위한 객관적인 자료를 제공한다.

• Macromolecular Research
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• 제15권4호
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• pp.302-307
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• 2007

The living radical polymerization of methyl methacrylate (MMA) by atom transfer radical polymerization, (ATRP) employing a $Fe(II)X_2/diphenyl-2-pyridyl$ phosphine (PyP) catalytic system (X=Cl, Br), was investigated using several initiators and solvents at various temperatures. Most of the polymerizations with the PyP ligand were well controlled, with a linear increase in the number average molecular weights ($M_n$) vs. conversion, with relatively low molecular weight distributions ($M_w/M_n=1.2-1.4$) throughout the reactions. The measured weights matched those of the predicted values. The ethyl-2-bromoisobutyrate (EBriB) initiated ATRP of MMA, with the $Fe(II)X_2/diphenyl-2-pyridyl$ phosphine catalytic system (X=Cl, Br), was better controlled in p-xylene at $80^{\circ}C$ than the other solvents used in this study.

• Nuclear Engineering and Technology
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• 제46권4호
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• pp.475-480
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• 2014

We developed a simple method to prepare the displacement damage cross section of SiC using NJOY and SRIM/TRIM. The number of displacements per atom (DPA) dependent on primary knock-on atom (PKA) energy was computed using SRIM/TRIM and it is directly used by NJOY/HEATR to compute the neutron energy dependent DPA cross sections which are required to estimate the accumulated DPA of nuclear material. SiC DPA cross section is published as a table in DeCART 47 energy group structure. Proposed methodology can be easily extended to other materials.

• 한국분말재료학회지
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• 제10권4호
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• pp.288-293
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• 2003

Mechanical alloying (MA) by high energy ball mill of Pure chromium Powders was carried out under the nitrogen gas atmosphere. Cr-N amorphous alloy powders have been produced through the solid-gas reaction subjected to MA. The atomic structure during amorphization process was observed by X-ray and neutron diffractions. An advantage of the neutron diffraction technique allows us to observe the local atomic structure surrounding a nitrogen atom. The coordination number of metal atoms around a N atom turns out to be 5.5 atoms. This implies that a nitrogen atom is located at both of centers of the tetrahedron and octahedron formed by metal atoms to stabilize an amorphous Cr-N structure. Also, we have revealed that a Cr-N amorphous alloy may produced from a mixture of pure Cr and Cr nitrides powders by solid-solid reaction during mechanical alloying.

• Macromolecular Research
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• 제17권8호
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• pp.557-562
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• 2009

The free radical polymerization of styrene was initiated with azobis(isobutyronitrile) in the presence of benzene sulfonyl chloride. Analysis of the terminal structures of the obtained polystyrene with $^1H$ NMR spectroscopy revealed the presence of a phenyl sulfonyl group at the ${\alpha}$-end and a chlorine atom at the ${\omega}$-end of each polystyrene chain. The terminal chlorine atom in the polystyrene chains was further confirmed through atom transfer radical polymerization (ATRP) of styrene and methyl acrylate using the obtained polystyrenes as macroinitiators and CuCl/2,2'-bipyridine as the catalyst system. GPC traces of the products obtained in ATRP at different reaction times were clearly shifted to higher molecular weight direction, indicating that nearly all the macroinitiator chains initiated ATRP of the second monomers. In addition, the number-average molecular weights of the polystyrenes increased directly proportional to the monomer conversions, and agreed well with the theoretical ones.

• Bulletin of the Korean Chemical Society
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• 제12권3호
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• pp.265-270
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• 1991

Theoretical calculations on the stabilization energies of framework atoms in hydrolyses Co(Ⅱ )-exchanged zeolite A were made using some potential energy functions and optimization program. The protons which are produced by hydrolysis of $[Co(H_2O)_n]^{2+}$ ion in large cavity showed a tendency to attack the framework oxygen atom O(1) preferentially, and the oxygen atom O(4) within OH- ion was coordinated at Al atom. The weakness of bonds between T(Si, Al) and oxygen by attack of proton and too large coordination number around small aluminum atom will make the framework of Co(Ⅱ)-exchanged zeolite A more unstable. The stabilization energy of $Co_4Na_4$-A framework (- 361.57 kcal/mol) was less than that of thermally stable zeolite A($Na_{12-}$A: - 419.68 kcal/mol) and greater than that of extremely unstable Ba(Ⅱ)-exchanged zeolite A($Ba_{6-}$A: - 324.01 kcal/mol). All the data of powder X-ray diffraction, infrared and Raman spectroscopy of Co(Ⅱ)-exchanged zeolite A showed the evidence of instability of its framework in agreement with the theoretical calculation. Three different groups of water molecules are found in hydrated Co(Ⅱ )-exchanged zeolite A; W(Ⅰ) group of water molecules having only hydrogen-bonds, W(Ⅱ) group water coordinated to $Na^+$ ion, ans W(Ⅲ) group water coordinated to Co(Ⅱ) ion. The averaged interaction energy of each water group shows the decreasing order of W(Ⅲ)>W(Ⅱ)>W(Ⅰ).

• 한국자기학회지
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• 제22권5호
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• pp.157-161
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• 2012

각기 암염구조를 가지는 sp 반쪽금속인 NaN과 CaN가 계면상태를 이룰 때의 반쪽금속성 및 자성을 연구하기 위해 단순계면계와 혼합계면계 두 계를 고려하여, FLAPW(full-potential linearized augmented plane wave) 방법을 이용하여 그 전자구조를 계산하였다. 계산된 원자별 자기모멘트를 보면, 단순계면계에서는 Na 쪽 계면 N 원자의 자기모멘트는 안쪽 N 원자에 비해 다소 감소하였고, Ca 쪽 계면 N원자의 경우는 다소 증가하였다. 혼합계면계에서는 계면 N 원자들의 자기모멘트는 대략 덩치 CaN과 NaN에서 N 원자의 자기모멘트 값의 평균치를 가졌으나, 아래 위층 모두에서 Na와 연결된 계면 N 원자의 자기모멘트가 가장 컸고, 아래 위층 모두에서 Ca 원자와 연결된 계면 N 원자의 자기모멘트가 가장 작았다. 이와 같은 상황은 각각의 N 원자가 이웃한 Ca나 Na 원자와 결합하면서 결합에 참여하지 않은 p 전자수가 자기모멘트의 크기를 결정한다는 사실과 부합한다. 또한 계산된 원자별 상태밀도를 통해 이들의 계면상태를 논의하였다.