• Journal of the Korean Crystal Growth and Crystal Technology
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• v.3 no.2
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• pp.167-175
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• 1993

Lithium-Carbon Intercalation Compounds(Li-CICs) have been synthesized from various carbon ma-terials by use of the modified stainless steel two-bulbs methods. These compounds had various colours by structural character of starting materials. The synthesized Li-CICs were identified to stage formation process by X-ray diffraction data. At these results, well-oriented natural graphite and graphite fiber are formed lower stages(Stage 1, Stage 2), but poor-oriented carbon fiber and petroleum cokes are also formed higher stages(Stage 3, Stage 4, Stage 5). And when we compared with measured d value and calculated d value, these values agreed with each other. But poor-oriented carbon materials are some difference from them. The stage stability and energy stage of Li-CICs were obtained by UV/VIS Spectrophotometric data. X-ray diffraction and UV/VIS Spectrophotometric data suggested that well-oriented carbon materials has distingushible curve between energy and reflectance. In these results, we know that many charge carriers between carbon layers are related to concentration of intercalants. And then, this paper also provides information on high efficiency energy storing materials at intercalation process of Li-CICs.

• Proceedings of the Computational Structural Engineering Institute Conference
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• 2011.04a
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• pp.400-403
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• 2011

본 논문에서는 시차열중량분석법과 X-선 회절분석법을 이용한 원전콘크리트의 탄산화에 의한 열화도 평가를 진행하였으며 두 가지 정성적 분석방법을 이용한 반정량적 평가 방법을 개발하였다. 원자력발전소 건설에 사용된 동일한 콘크리트 배합을 사용한 시편을 촉진 탄산화 시험장치에 28, 56, 91, 180, 365일 기간에 걸쳐 노출시켜 탄산화를 진행하였으며 노출된 시편은 시차열중량분석법, X-선 회절분석법을 이용하여 탄산화에 따라 발생된 열화생성물의 양을 정성적으로 분석하였다. 그 결과, 탄산화로 인해 발생되는 Calcite의 양이 노출기간에 따라 점차적으로 증가되는 것이 확인되었으며, Calcite의 생성을 위해 이산화탄소와 반응하는 Portlandite의 양이 점차적으로 감소되는 것이 확인되었다. 본 논문에서는 위의 언급된 두 방법의 관계성을 통해 열화도 평가를 진행하였다.

• Journal of the Korean Magnetics Society
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• v.8 no.4
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• pp.198-202
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• 1998

We have studied $Al_xFe_{3-x}O_4$ produced by direct composition method using X-ray diffraction and Mssbauer spectroscopy. The cation distribution for $Al_xFe_{3-x}O_4$ was determined by the ratio of sub-spectra absorption area. The charge state of Fe atoms in octahedral site(B-site) is $Fe^{2.5+}$ based on electron hopping, $Fe^{2+}$ ↔ $(Fe^{3+},Al^{3+})$ without dependency of substituted Al amounts.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.7 no.2
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• pp.197-206
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• 1997

A SiC epilayer on the 6H-SiC crystal substrate was grown by chemical vapor deposition (CVD). The crystal structure of the SiC epilayer was investigated by using the X-ray diffraction patterns and the Roman scattering spectroscopy. The SiC epilayer on the 6H-SiC substrate was grown to be homoepilayer by CVD. In order to distinguish a certain SiC polytype mixed in the SiC crystal grown by the modified Lely method, we have calculated the X-ray diffraction intensities and Brags angles of the typical SiC crystal powders. By comparing the measured X-ray diffraction pattern with the calculated ones, it was identified that the SiC crystal grown by the modified Lely method was the 6H-SiC crystal mixed some 15R-SiC.

• Korean Journal of Crystallography
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• v.8 no.2
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• pp.132-137
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• 1997

The crystal structure of N,N'-di-tert-butoxycabonyl-2,7-diazabicyclo[3.3.0]oct-4-ene has been determined from single crystal x-ray diffraction study; C16H26N2O4, Triclinic, P1, a=11.119(1) Å, b=13.638(1) Å, c=6.214(1) Å, α=92.14(1)°, β=103.49(1)°, γ=73.35(1)°, V=877.4(2)Å3, T=293(2)K, Z=2, CuKα(λ=1.5418Å). The structure was solved by direct method and refined by full-matrix least squares to a final R=5.38% for 2389 unique observed F0>4σ(F0) reflections and 225 parameters.

• Korean Journal of Crystallography
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• v.8 no.2
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• pp.138-143
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• 1997

The crystal structure of isoimperatorin, f-[(3-methyl-2-butenyl)oxy]-7H-furo[3,2-g][1] benzopyran-7-one, has been determined from single crystal x-ray diffraction study; C16H14O4, Monoclinic, P21/c, a=8.865(1) Å, b=9.331(1) Å, c=16.156(1) Å, β=98.12(1)', V=1322.9(2) Å3, T=293(2)K, z=4, Cu Kα(λ=1.5418 Å). The structure was solved by direct method and refined by full-matrix least squares to a final R=5.72% for 1922 unique observed Fo>4o(F0) reflections and 182 parameters.

• Korean Journal of Crystallography
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• v.6 no.1
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• pp.27-35
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• 1995

The crystal structure of 1-tert-butoxycarbonyl-4-[N-(tert-butoxycarbonyl)-N-(ethoxycarbonylmethyl)amino]-3-phenylsulfonylpyrrolidind [C24H36O8N2S] has been from single crystal x-ray diffraction study ; C24H36O8N2S triclinic, p1, a=11.363(8)Å, b=11.589(6)Å, c=11.013(10)Å,α=95.32(6)°,β=98.64(7)°,γ=79.57(5)°,V=1406.8(18)Å3, t=293K, Z=2, CuKα(λ=1.5418Å). The molecular structure was solved by diredt method and refined by full-matrix least squares to a final R=9.78% for 3621 unique observed [F≥4σ(F)] reflections and 703 paramenters.

• Korean Journal of Crystallography
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• v.6 no.2
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• pp.98-102
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• 1995

The crystal structure of -Ethyl-1,4-dihydro-7-methyl-1,8-naphthyridin-4-one-3-carboxylic acid [Nalicixic Acid] has been determined from single crystal X-ray diffraction study; C12H12N2O3, monoclinic, P21/c, a=8.910(2)Å, b=13.145(3)Å, c=9.370(3)Å, β =100.06(2)°, V=1080.6Å, T=293K, Z=4, CuKα(λ=1.5418Å). The molecular structure was solved by direct method and refined by full-matrix least squares to a final R=0.055 for 1555 unique observed [F0>4σ(F0)] reflections and 166 parameters. The conformation of the molecule is stabilized by an intramolecular O(17)-H(17)…O(14) hydrogen bond [2.525(2)Å, 144.3(10)°].

• Electrical & Electronic Materials
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• v.5 no.3
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• pp.271-277
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• 1992

X-선 회절 분석 및 적외선 투과율 측정은 실온에서 수행되었다. 또한 $Y_{1-x}$Nd$_{x}$Ba$_{2}$Cu$_{3}$O$_{7-y}$고온초전도체의 자기 임계전류밀도와 저항은 각각 30K와 80-140K 범위의 온도에서 조사되었다. 시료들은 고상 반응법에 의해서 제조되었다. 시료들의 결정구조는 X-선 회절무늬로 부터 모두 직방정계임이 판명되었다. 한편 x의 양이 증가함에 따라서 전이온도 T$_{c}$는 88K 근처의 값을 가지며 x의 양이 증가함에 따라 약간 감소하였다. 적외선 투과율 측정에서 날카로운 peak들은 472.23-618.87$cm^{-1}$ / 범위에 있었다. 이것은 특이할 정도로의 low-lying plasmalike edge와 낮은 에너지의 전자적인 여기가 존재함을 나타내는 것이다. 자기임계 전류밀도는 $10^{2}$~$10^{3}$A/$cm^{2}$ 범위에 있었다.있었다.

• Korean Journal of Crystallography
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• v.9 no.2
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• pp.138-142
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• 1998

Lithium triborate, LiB3O5(Mr=119.37), 단결정을 상단 종자정 융액법으로 성장시켰으며, 결정구조를 X-선 회절법으로 연구하였다. 결정계는 사방정계이며 공간군은 Pna21(No. 33)이다. 단위포의 상수는 a=8.432(1) , b=7.364(1) , c=5.110(1) , α=β=γ=90.00o, V=317.3(6) 3, V=4, Dx=2.50 gcm-3, MoKα1, λ=0.71069 , μ=2.3/cm, F(000)=232, T=293 K 이었다. 최종 구조의 오차인자는 520개 회절 점에서 각각 R=0.0222과 wR=0.0582이었다.