• Bulletin of the Korean Chemical Society
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• 제20권10호
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• pp.1205-1208
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• 1999

27Al NMR chemical shielding, quadrupolar coupling, and dipolar coupling interactions for corundum (α-Al2O3) are determined from the single-crystal 27 Al NMR spectra according to the rotation about three orthogonal axis. 27 Al NMR parameters obtained in this work with high accuracy are as follows: δiso = 7.4(4) ppm, QCC = 2.30(4) MHz, h = 0.08(3), and R = 2.0(3) kHz. This work appears to be the first NMR measurement of an aluminum-aluminum dipolar coupling interaction in α-Al2O3 crystals.

• 한국표면공학회지
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• 제33권5호
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• pp.365-372
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• 2000

Pure $Fe_3$Al alloys with three different compositions of Fe-21.8%Al, Fe-24.1%Al and Fe-27.2%Al were prepared by vacuum induction melting followed by homogenization and hot forging. The long-time oxidation behavior of the prepared alloys was studied at 1073, 1273 and 1473k in air. The oxidation resistance greatly increased with an increase in Al contents. Thin and uniform oxide scales were always formed on Fe-27.2%Al, while thick and fragile oxide scales were formed on Fe-(21.8, 24.1%)Al. Internal oxidation was observed in Fe-(21.8, 24.1%)Al, when oxidized above 1273K. The major oxidation product of all the oxidized alloys was always $\alpha$-$Al_2$$O_3$.

• 한국자기공명학회논문지
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• 제16권2호
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• pp.111-121
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• 2012

The spin-lattice relaxation times, $T_1$, and spin-spin relaxation times, $T_2$, of the $^{27}Al$ and $^{87}Rb$ nuclei in $RbAl(CrO_4)_2{\cdot}2H_2O$ crystals were investigated. The presence of only one resonance line for the $^{27}Al$ nuclei indicates that the results in a dynamical averaging of the crystal electric field that produces a cubic symmetry field. The changes in the temperature dependence of $T_1$ are related to variations in the symmetry of the octahedra of water molecules surrounding $Al^+$ and $Rb^+$. The $T_1$ values for the $^{27}Al$ and $^{87}Rb$ nuclei are different due to differences in the local environments of these ions. We also compared these $^{27}Al$ and $^{87}Rb$ NMR results with those obtained for $RbAl(CrO_4)_2{\cdot}2H_2O$ crystals. The relaxation mechanisms of $RbAl(XO_4)_2{\cdot}nH_2O$ (X=Cr and S) crystals are characterized by completely different NMR behaviors.

• 한국주조공학회지
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• 제24권6호
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• pp.356-365
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• 2004

Mechanical properties and microstructures of the Ni-AI-Fe and Ni-AI-Fe-(B, Zr) alloys which containing $10{\sim}30at$.%Fe, 0.1at.%B and/or 0.1at.%Zr have been investigated. The experimental results showed that the microstructures of Ni25Al were changed from a single phase ${\gamma}$ to dual phase ${\gamma}$ and ${\beta}$ by addition of 27at.%Fe. Ni45Al, however, kept the single ${\beta}$ phase even though Fe was added upto 30at.%. The hardness of Ni25Al were increased from $H_RB$ 70 to $H_RC$ 39 by addition of 27at.%Fe. In the case of Ni45Al which have $H_RC$ 37, the hardness was decreased by lOat.%Fe addition, but increased with 30at.%Fe. The yield strength and ultimate compressive strength in the compressive test have showed a similar trend with the hardness change. The strain to fracture was 14% at maximum and achieved in Ni25Al-27at.%Fe and Ni25Al-27at.%Fe-0.1 at.%B alloys. The Ni45Al showed a relatively low strain to fracture as 4%. The impact absorption energy of Ni25Al increased from 0.74 kg-m to 1.81 kg-m by addition of 27at.%Fe. In case of Ni45Al, the addition of lOat.%Fe and lOat.%Fe with small amounts of Band Zr did not change significantly the impact absorption energy of 0.60 kg-m, whereas the addition of 30at.%Fe with small amounts of B and Zr increased it slightly. In fracture tests, both of two basic materials showed the same intergranular fracture but by adding Fe it changed to the cleavage fracture mode or co-existing of cleavage and intergranular fractures.

• 한국세라믹학회지
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• 제40권8호
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• pp.720-724
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• 2003

Aluminum nitride (AlN) powders were synthesized by using a mixture of an aluminum nitrate or sulfate salt and carbon (mole ratio of $Al^{3+}$ to carbon=L : 30). The AlN was obtained by calcining the mixture under a flow of nitrogen in the temperature range 1100-1$600^{\circ}C$ and then burning out the residual carbon. The process of conversion of the salt to AlN was monitored by XRD and $^{27}$ Al magic-angle spinning (MAS) NMR spectroscopy. The salt decomposed to ${\gamma}$-alumina and then converted to AlN without phase transition from ${\gamma}$-to-$\alpha$-alumina. $^{27}$ Al MAS NMR spectroscopy shows that the formation of AlN commenced at 110$0^{\circ}C$. AlN powders obtained from the sulfate salt were superior to those from the nitrate salt in terms of homogeneity and crystallinity. A very small amount of AlN whiskers was obtained by calcining a mixture of an aluminum sulfate salt and carbon at 115$0^{\circ}C$ for 40 h, and the growth of the whiskers is well explained by the particle-to-particle self-assembly mechanism.

• 한국전기화학회:학술대회논문집
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• 한국전기화학회 2001년도 춘계총회 및 학술발표회
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• pp.27-27
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• 2001

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 1994년도 추계학술대회강연 및 발표대회 강연및 발표논문 초록집
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• pp.27-27
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• 1994

• 한국광물학회지
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• 제28권1호
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• pp.61-69
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• 2015

현무암과 포놀라이트 조성을 가진 마그마는 분화 양상과 거시적 물성에서 많은 차이를 보이나 이에 대한 원자구조 단위의 근본적인 원인은 아직 명확히 밝혀지지 않았다. 본 연구에서는 일차원과 고해상도 이차원 고상 핵자기공명 분광분석(Nuclear Magnetic Resonance, NMR)을 이용하여 현무암질 마그마의 모델인 투휘석과 아노르다이트 공융점 조성을 가진 비정질 규산염과 포놀라이트 조성의 비정질 규산염의 Al 주변 원자 구조를 관찰하였다. $^{27}Al$ MAS NMR 실험 결과 두 조성 모두 Al 피크가 지배적인 것을 보여주며 현무암 조성의 비정질 규산염의 피크 반치폭이 포놀라이트 조성보다 약 2배 더 넓은 것으로 관찰된다. 이것은 현무암질 조성에서의 Al 주변의 위상 무질서도가 포놀라이트 조성보다 높다는 것을 의미한다. $^{27}Al$ 3QMAS NMR 실험 결과 Al과 Al이 구별되어 관찰되며 현무암 조성의 비정질 규산염에서 포놀라이트 조성에는 관찰되지 않는 Al이 약 3.3% 관찰된다. 이는 현무암질 마그마가 포놀라이트 마그마에 비해 Al 주변의 배열 무질서도가 더 큰 것을 의미한다. 사중극자 상호관계를 설명하는 계수 또한 현무암 조성의 비정질 규산염이 포놀라이트 조성의 비정질 규산염에 비해 큰 값을 나타내며 이것 또한 Al 주변의 위상 무질서도가 더 큰 것을 확증해준다. 본 논문에서 규명한 현무암과 포놀라이트 조성의 비정질 규산염의 원자 구조 차이는 점성도와 같은 조성에 따른 마그마의 물성 차이에 대한 미시적 기원을 제시한다.

• 한국자기공명학회:학술대회논문집
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• 한국자기공명학회 2002년도 제20회 학술발표회
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• pp.22-22
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• 2002

• 대한화학회지
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• 제40권10호
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• pp.656-662
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• 1996

저온상압법에 의해 Si/Al의 비가 100정도되는 ZSM-5를 합성하였으며 시간 경과에 따른 결정화과정을 $^{27}Al$ 및 $^{29}Si$ MAS NMR spectea 및 FT-IR로 고찰하였다. 저온상압 하에서 합성한 결과 초기 반응물질 및 성분비에 따라 화학적 이동은 기종의 연구와는 다른 경향을 보였으나 반응이 진행됨에 따라 최종 생성물의 화학적 이동은 전형적이 ZSM-5 영역에서 나타나고 있음을 확인하였다. 그리고 국부결함은 소성에 의해 제거되었으며 최종생성물의 XRD 및 SEM의 결과에서도 합성된 물질이 ZSM-5임을 확인하였다.