• 한국전기전자재료학회논문지
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• 제24권9호
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• pp.760-765
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• 2011

Znic sulfide (ZnS) thin films were deposited on glass substrates by radio frequency magnetron sputtering. The substrate temperature varied from room temperature (RT) to $500^{\circ}C$. The structural and optical properties of ZnS films were studied by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive analysis of X-ray (EDAX) and UV-visible transmission spectra. The XRD analyses reveal that ZnS films have cubic structures with (111) preferential orientation, whereas the diffraction patterns sharpen with the increase in substrate temperatures. The FESEM images indicate that ZnS films deposited at $400^{\circ}C$ have nano-sized grains with a grain size of ~ 67 nm. Then films exhibit relatively high transmittance of 80% in the visible region, with an energy band gap of 3.71 eV. One obvious result is that the energy band gap of the film increases with increasing the substrate temperatures.

• 한국식품과학회지
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• 제30권5호
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• pp.1024-1028
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• 1998

압출성형 방법에 의하여 고아밀로즈 옥수수전분으로부터 제조된 난소화성 전분의 분자구조적 특징을 규명하기 위하여 X-ray 회절 실험과 $^{13}C\;NMR$ 분석을 시도하였다. X-ray를 이용한 전분구조분석에서 전분의 결정 구조 비율은 압출성형시 낮은 바렐온도 $(100^{\circ}C)$에서는 원료투입 수분함량 증가시$(25{\sim}45%)$ 6.08%에서 8.37%로 약간 증가하는 경향을 보였으며, 시료간의 큰 차이는 보이지 않았다. X-ray pattern에서 $Peak\;2{\theta}$ 비교시 고 아밀로즈 압출성형물이 투입원료 수분함량이 감소하고$(45\;{\rightarrow}\;25%)$, 바렐온도가 상승하면$(120\;{\rightarrow}\;140^{\circ}C)$ 결정격자 간격 d가 작은 조밀한 결정구조가 붕괴되고 d가 증가한 느슨한 결정구조로 변형됨을 알 수 있다. $4^{\circ}C$ 저장중 압출성형된 고아밀로즈 옥수수 전분 결정 비율은 4주 저장 후에$(6.3{\sim}8.3%)$에서$(4.5{\sim}5.8%)$로 약간 감소되는 결과를 나타내었다. $^{13}C\;NMR$ 실험을 통한 이중나선 구조 비율은 바렐온도 상승시, 투입원료 수분함량이 적을수록 그 비율이 60%에서 42.5%로 감소되었고 저장 중에는 큰 변화를 보이지 않았다. 전보에서 발표한 pancreatin에 의한 난소화성 전분 수율과 비교해 보면, 이중 나선구조 구성 비율은 저장전에는 서로 상관관계가 있어 보이나 저장중 변화에서는 서로 연관성을 나타내지 않았다. 즉, 저장중 난소화성 전분수율의 증가는 X-ray 분석에 의한 상대적 결정성화가 약간 감소하면서 이중나선구조 비율에는 변화가 없는 특징적 분자구조 변형에 의한 것이라 사료된다.

• Bulletin of the Korean Chemical Society
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• 제33권4호
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• pp.1242-1246
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• 2012

The Co oxide microfibers were synthesized using the electrospinning process and formed $Co_3O_4$ microfibers after being calcined at high temperatures. The calcination temperature influenced the diameters, morphology, crystalline phase, and chemical environment of the fibers. The surface morphology of the obtained fibers was examined by using the scanning electron microscope (SEM). As the calcination temperatures increased from room temperature to 873 and 1173 K, the diameters of the cobalt oxide fibers decreased from 1.79 to 0.82 and 0.32 mm, respectively. The structure of the fibers was investigated with X-ray diffraction (XRD) and transmission electron microscopy (TEM). The calcined $Co_3O_4$ fibers had crystalline face-centered cubic (fcc) structure. The X-ray photoelectron spectroscopy (XPS) results revealed that increasing the calcination temperature promoted the formation of $Co^{2+}$ and $Co^{3+}$ species.

• 에너지공학
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• 제24권2호
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• pp.55-58
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• 2015

The mesoporous metal organic framework structure Fe-BTC was successfully synthesized by hydrothermal process with noticeable yield. The synthesis operation was conducted at intermediate temperature and for shortened operation time as compared to conventional procedures. This process approach with reduced operating temperature and shortened operation time may open an opportunity window towards process economy with reduction in energy consumption. A simple mathematical approach of diffraction indexing using X-ray diffraction patterns of synthesized powder was employed to confirm its crystalline nature and to investigate its high temperature stability. The crystallite size was calculated by using Debye-Scherrer equation.

• Journal of Korean Vacuum Science & Technology
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• 제4권2호
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• pp.50-54
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• 2000

We studied the synthesis of S $i_{1-x}$ Cx (x=0.016) epitaxial layer using ion implantation and solid phase epitaxy (SPE). The activation energy Ea was obtained for the loss of substitutional carbon using fourier transform-infrared spectroscopy (FTIR) and high-resolution x-ray diffraction (HR-XRD). In FTIR analysis, the integrated peak intensity was used to quantify the loss of carbon atoms from substitutional to interstitial sites during annealing. The substitutional carbon contents in S $i_{0.984}$ $C_{0.016}$ were also measured using HR-XRD. By dynamic simulations of x-ray rocking curves, the fraction of substitutional carbon was obtained. The effects of annealing temperature and time were also studied by comparing vacuum furnace annealing with rapid thermal annealing (RTA))))))

• 청정기술
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• 제20권1호
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• pp.28-34
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• 2014

본 연구에서는 나노 크기의 결정 구조를 가진 타이타니아 담체를 용매열합성법(solvothermal method)을 활용하여 합성한 후 팔라듐과 구리를 담지한 촉매를 제조하였다. 제조된 촉매를 수중 질산성 질소 저감 반응에 적용한 결과, 타이타니아 담체의 결정 크기가 반응 활성에 영향을 미치는 것이 확인되었다. 결정 크기가 작은 담체를 활용한 촉매가 더 빠른 속도로 질산성 질소를 저감하였지만, 반응 중 pH가 높게 형성되어 질소 선택도가 매우 낮은 현상을 보였다. 이를 해결하기 위해 pH 완충제인 이산화탄소를 공급하여 질소 선택도를 약 60% 증가시켰다. 상기에 언급한 촉매를 대상으로 질소 흡-탈착, X-ray diffraction (XRD), $H_2$-temperature programmed reduction (TPR), X-ray photoelectron spectroscopy (XPS) 등의 다양한 특성화 분석을 수행하여 촉매의 반응활성과 물성간의 상관관계에 대해 조사하였다.

• 자원리싸이클링
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• 제3권3호
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• pp.21-26
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• 1994

국내에서 산출되고 있는 반토혈암으로부터 고순도 $\alpha-Al_2O_3$를 얻기 위하여 황산암모늄을 사용한 염배소와 황산을 이용한 추출 그리고 하소 실험을 하였다. 황산의 농도, 반응시간, 온도 등이 알루미나 추출에 미치는 영향에 대하여 조사하였으며, 반응산물은 X-ray, DTA-TG, 화학분석, SEM 등으로 분석하였다. 추출조건은 전처리 조건으로 황산암모늄의 농도가 0.6M, 배소온도가 $650^{\circ}C$였으며, 황산추출은 황산농도 10%로 240분간 추출할 경우 96%의 수율을 나타내었다. 생성된 $Al_2O_3$ 분말을 X-ray 분석한 결과 $\alpha-Al_2O_3$였으며 그 순도는 99.23%였다.

• 대한전자공학회논문지
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• 제23권5호
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• pp.706-711
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• 1986

The AgGa1-xInxSe2 films are deposited by a flash evaporation method onto pyrex glass substrates at temperatures between 5\ulcorner and 360\ulcorner. The single crystalline films which have X-ray diffraction peak of only (112) plane are preared at substrate temperature above 360\ulcorner. The prepared AgGa 1-xInxSe2 films are high photosensitive. The temperature coefficients of energy gap are found to be (-1.2~-4.0)x10**4 eV/K and (-3.1~-5.2)x10**-4 eV/K, and that of peak energy of spectral photoresponse curve are found to be (-1.1 ~ -3.0)x10**-4 eV/K(50K~100K) and (-2.4~-5.1)x10**-4 eV/K(100K~300K).

• Bulletin of the Korean Chemical Society
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• 제16권7호
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• pp.600-603
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• 1995

A series of samples in the Sm1-xSrxCoO3-y(x=0.00, 0.25, 0.50, 0.75 and 1.00) system has been prepared at 1200 ℃ under ambient atmosphere. The X-ray diffraction patterns of the samples with x=0.00 and 0.25 are indexed with orthorhombic symmetry like GdFeO3 and x=0.50 appears to be perfectly cubic. In the tetragonal system (x=0.75), the structure is similar to that of SrCoO2.80. The composition of x=1.00, SrCoO2.52, shows the brownmillerite-type structure. The reduced lattice volume is increased with x value in this system. The chemical analysis shows the τ value (the amount of the Co4+ ions in the system) is maximized at the composition of x=0.50. Nonstoichiometric chemical formulas are determined by the x, τ and y values. The electrical conductivity has been measured in the temperature range of 78 to 1000 K. The activation energy is minimum for those of x=0.25 and x=0.50 with metallic behavior. First-order semiconductor-to-metal transition of SmCoO3 is not observed. Instead, a broad, high-order semiconductor-to-metal transition is observed. In general, the effective magnetic moment is increased with increasing τ values at low temperature. At high temperature, the magnetic moment is maximum for that of x=0.00. The 3d-electrons are collective and give ferromagnetism in x=0.50.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1999년도 추계학술대회 논문집
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• pp.221-223
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• 1999

In this work, samples were manufactured variously by changing conventional calcining and sintering conditions and we tried the utilization by making the heat treatment time, which is demanded to high-Tc phase formation, much shorter. We found out optimal heat treatment conditions with the analysis on formation process at superconducting phase in term of the change of calcining and sintering time and then, examined X-ray diffraction(XRD) patterns, scanning electron microscope(SEM) measurement and energy dispersive X-ray spectrometer(EDX) of the samples manufactured under heat treatment conditions which we suggest here. As a result, 2223 high-$T_c$, phase of (Bi,Pb)SrCaCuO superconductor starting with ($Bi_l$ xPbx,)$_2$$Sr_2$$Ca_2$$Cu_3$$O_y$, composition was formed from 1 hr sintering sample at temperature nearby melting point and also the completed sample with calcining and sintering time of 9 hr was formed high-$T_c$.low-$T_c$ phase appearing in sight above the critical temperature of liquid $N_2$.