• Fibers and Polymers
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• 제6권3호
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• pp.206-218
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• 2005

Structural studies of series of 'as spun' and drawn PEEK fibers have been carried out using X-ray diffraction and optical microscopy techniques. The analysis of results suggest that fibers produced at a constant draw ratio with increasing draw temperatures show enhanced orientation and crystalline behaviour. The resolved equatorial and meridional traces provide additional structural parameters in terms of crystallinity, crystallite size, and crystallite thickness. It is concluded that drawing at a temperature below $T_g(i.e.,\;144^{\circ}C)$ results in poorly oriented non-crystalline materials, whereas drawing above $T_g$ results in highly oriented semi crystalline materials. Additional drawing proved to increase the overall orientation with slight improvements in lateral order of the chain molecules. Quantitative analysis revealed that the crystallite size increases with increasing drawing temperature. The results also revealed the increased crystallite size upon additional drawing. Crystalline orientation parameter, $_c$, suggests almost perfect orientation. In all cases, the amorphous orientation is found to be lower than the overall orientation parameter obtained from the optical birefringence. As a result of additional drawing, crystalline orientation was found to increase slightly but the increase in the orientation of non-crystalline material was found to be substantial. An average crystalline density was determined from the orthorhombic unit cell dimensions. It was found to vary as a result of processing conditions. It was also found that the value of the maximum birefringence shows heavy dependence on the chain conformation.

• 한국근적외분광분석학회:학술대회논문집
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• 한국근적외분광분석학회 2002년도 강연요지집
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• pp.97-117
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• 2002

A chemoinfometrical method for quantitative determination of crystal content of indomethacin (IMC) polymorphs based on fourie-transformed near-infrared (FT-NIR) spectroscopy was established. A direct comparison of the data with the ones collected from using the conventional powder X-ray diffraction method was performed. Pure $\alpha$ and ${\gamma}$ forms of IMC were prepared using published methods. Powder X-ray diffraction profiles and NIR spectra were recorded for six kinds of standard materials with various content of ${\gamma}$ form IMC. The principal component regression (PCR) analyses were performed based on normalized NIR spectra sets of standard samples of known content of IMC ${\gamma}$ form. A calibration equation was determined to minimize the root mean square error of the prediction. The predicted ${\gamma}$ form content values were reproducible and had a relatively small standard deviation. The values of ${\gamma}$ form content predicted by two methods were in close agreement. The results were indicated that NIR spectroscopy provides for an accurate quantitative analysis of crystallinity in polymorphs compared with the results obtained by conventional powder X-ray diffractometry.

• 열처리공학회지
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• 제30권5호
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• pp.215-221
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• 2017

The effect of austenitizing temperature on the degree of carbides re-solutionizing, mean graine size, hardness and the volume fraction of retaind austenite ($V_{\gamma}$) etc., has been studied by means of metallography, X-ray diffractometry and hardness measurement in STD 11 tool steel. As austenitizing temperature increases, the amount of alloying elements which is re-dissolved into matrix increases, resulting in increase of $V_{\gamma}$, due to the chemical stabilization of austenite. The Vickers hardness value decreases with increasing austenitizing temperature, which is attributed to grain size as well the volume fractions of $V_{\gamma}$ and carbides. Theoretical diffraction intensity of (200) ${\alpha}^{\prime}$, (211) ${\alpha}^{\prime}$ (200) ${\gamma}$ and (220) ${\gamma}$ peaks obtained by $CuK_{\alpha}$ chracteristics X-ray (${\lambda}=0.15429nm$) was calculated, and quantitative analysis of $V_{\gamma}$ could be carried out by X-ray diffraction method. The resultant value is well coincided with the value obtained by image analysis method. When the quenched specimen is tempered above $200{\sim}400^{\circ}C$ for 30 min, the transition carbides i.e., MC and $M_2C$ in the size of about 20 nm begin to precipitate at $300^{\circ}C$.

• 한국광물학회지
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• 제19권4호
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• pp.363-381
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• 2006

거창화강석의 품질기준 설정을 위한 정확한 광물조성을 구하기 위하여 거창지역 석산을 포함하여 포천, 익산 및 중국에서 수입된 총 39개의 화강석 시료를 대상으로 현미경 육안관찰에 의한 광물모드 분석, X-선 형광분석에 의한 CIPW 노름 계산, 그리고 X-선 회절 데이터를 이용하여 리트벨트법에 의한 광물정량분석을 각각 실시하였다. 거창화강석은 회백색 내지 암색으로 중립질의 반상조직을 가지며, 구성광물은 석영, 사장석, 알칼리장석 및 흑운모가 우세하다 광물조성을 결정하기 위해 3가지 분석방법을 비교한 결과, 노름 계산은 화강암의 광물조성을 제대로 반영한다고 보기 어려우며, 현미경 육안관찰에 의한 모드 분석보다 X-선 회절 데이터를 이용한 리트벨트 정량법이 상대적으로 정확한 광물조성을 보여주는 것으로 판단된다. Q-A-P 삼각도에 작도한 결과, 거창화강석은 전형적인 화강섬록암의 광물조성을 보여주며, 포천화강석은 몬조화강암, 익산석은 몬조화강암 내지 화강섬록암, 그리고 중국거창석은 화강섬록암의 조성을 각각 보여준다. 특히 중국거창석과 비교하여 거창화강석이 광물조성으로는 전혀 구별이 되지 않는 유사한 조성을 보여준다.

• 한국세라믹학회:학술대회논문집
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• 한국세라믹학회 2000년도 춘계총회,특별강연,심포지움,연구발표회
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• pp.21.1-21.1
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• 2000

• 한국산학기술학회논문지
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• 제18권10호
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• pp.97-101
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• 2017

X-선 회절기(X-ray diffractometer)는 시편에서 회절되는 회절빔을 이용하여 재료의 상 (phase), 집합조직 (texture), 격자상수 (lattice constant), 잔류응력 (residual stress) 등 다양한 재료물성을 분석하는 데 광범위하게 사용되는 장치이다. X-선을 이용한 정량적인 분석은 회절빔의 피크 위치를 바탕으로 수행되는 데, 장시간 X-선 회절기를 사용하게 되면 필연적으로 장치 부품에 미세 변형이 발생하게 되고, 이러한 기계적인 오차가 발생하면 정량적인 분석의 정확도가 떨어지게 된다. 본 연구에서는 미국 표준기술연구소 (National Institute of Standards and Technology, NIST)에서 제공된 잔류응력이 없는 Si 파우더를 이용하여 $2{\theta}$를 기준으로 약 30~90도 사이 구간에 대해 X-선 회절 실험을 수행하였고, NIST에서 제공된 회절빔의 피크 위치와의 비교를 통하여 X-선 회절기의 계통오차를 파악하였으며, 이러한 오차 교정이 진격자상수 (true lattice constant) 측정 등 정량적인 분석에 미치는 영향을 확인하기 위하여 잔류응력이 존재하는 180 nm 두께의 텅스텐 박막에 대한 X-선 회절 분석을 수행하였다.

• The Journal of Advanced Prosthodontics
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• 제11권5호
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• pp.253-261
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• 2019

PURPOSE. To evaluate the influence of cyclic loading on phase transformation of zirconia abutments and to compare the effectiveness of three different quantitative ageing assessment techniques. MATERIALS AND METHODS. Thirty two Y-TZP prostheses fabricated from two brands, InCoris ZI and Ceramill ZI, were cemented to titanium bases and equally divided into two subgroups (n=8): control group without any treatment and aged group with cyclic loading between 20 N and 98 N for 100,000 cycles at 4 Hz in distilled water at $37^{\circ}C$. The tetragonal-to-monoclinic phase transformation was assessed by (i) conventional x-ray diffraction (XRD), (ii) micro x-ray diffraction (${\mu}XRD$), and (iii) micro-Raman spectroscopy. The monoclinic-phase fractions (M%) were compared by two-way ANOVA. RESULTS. InCoris Zi presented significantly higher M% than Ceramill Zi in both control and aged groups (P<.001). Both materials exhibited significant phase transformation with monoclinicphase of 1 to 3% more in aged groups than controls for all three assessment techniques. The comparable M% was quantified by both ${\mu}XRD$ and XRD. The highest M% was assessed with micro-Raman. CONCLUSION. Cyclic loading produced significant phase transformation in tested Y-TZP prostheses. The micro-Raman spectroscopy could be used as an alternative to XRD and ${\mu}XRD$.

• 한국방사선학회논문지
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• 제6권6호
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• pp.477-481
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• 2012

엑스선 회절분석기는 비파괴적인 방법으로 시료의 정보를 정성 및 정량적으로 분석할 수 있다. 엑스선 회절분석기에는 다양한 광학소자가 사용된다. 평행빔 광학소자는 광축에 평행한 빔을 통과시키고 발산하는 빔을 제거하는 역할을 한다. 와이어 컷 제작과 스테인리스 스틸 평판을 연마하여 평행빔 광학소자를 제작하였고 엑스선 영상장치를 이용하여 그 평행도를 평가하였다. 설계된 6 mrad과 매우 가까운 6.6 mrad의 평행도를 갖는 평행빔 광학소자를 제작하였다. 엑스선 영상을 이용하면 개개의 평판의 평행도를 예측할 수 있을 뿐만 아니라 다양한 광학소자 평가에도 사용될 수 있을 것이다.

• 복식
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• 제58권5호
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• pp.211-231
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• 2008

To conserve historic textiles, analyses of textile materials, pollutants and deterioration are prerequisite steps. Based upon analytical results, guides for conservation of historic textiles are established. In analyses of textile materials, pollutants and deterioration, there are chemical methods(burning, solubility and staining), physical methods(microscopy and density) and instrumental analysis(Fourier Transform Infrared Spectroscopy (FT-IR), Fourier Transform Raman Spectroscopy(FT-Raman), Gas Chromatography(GC), Mass Spectroscopy(MS), X-Ray Fluorescence (EDXRF, WDXRF), Energy Dispersive Spectroscopy(EDS), and X-Ray Diffraction(XRD), Tensile Testing Machine etc.). Combination of qualitative and quantitative analyses makes accurate diagnosis of textile condition possible. As examples of analyses and conservation of historic textiles, Chuninsan(19 century) similar to sunshade with handing down historic textile and golden decorative skirt(17 century) with excavated costume are taken.

• 한국근적외분광분석학회:학술대회논문집
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• 한국근적외분광분석학회 2001년도 NIR-2001
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• pp.2111-2111
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• 2001

A chemoinfometrical method for evaluating the quantitative determination of crystallinity one polymorphs based on fourie-transformed near-infrared (FT-NIR) spectroscopy was established. A direct comparison of the data with the ones collected from using the and compared with the conventional powder X-ray diffraction method was performed. [Method] The pPure a and g forms of indomethacin (IMC) were prepared by reportedusing published methods. Six kinds of standard samples obtained by physically mixing of a and g forms. After the powder X-ray diffraction profiles of samples have been measured, the intensity values were normalized to against the intensity of silicon powder as the as an external standard. The calibration curves for quantification of crystal content were based upon the total relative intensity of four diffraction peaks from of the form g crystal. FT-NIR spectra of six calibration sample sets were recorded 5 times with the NIR spectrometer (BRAN+LUEBBE). Chemoinfometric analysis was performed on the NIR spectral data sets by applying the principal component regression (PCR). [Results] The relation between the actual and predicted polymorphic contents of form g IMC measured using by the X-ray diffraction method shows a good straight linen linear relation., and it has slope of 0.023, an intercept of 0.131 and a correlation coefficient of 0.986. PCR analyses wereis was performed based on normalized NIR spectra sets offer standard samples of known content of IMC g form. IMC. A calibration equation was determined to minimize the root mean square error of the predictionthe prediction. Figure 1 shows a plot of the calibration data obtained by NIR method between the actual and predicted contents of form g IMC. The predicted values were reproducible and had a smaller standard deviation. Figure 2 shows that the plot for the predicted transformation rate (%) of form a IMC to form g as measured by X-ray diffractomeoy against to those as measured by NIR method. The plot has a slope of 1.296, an intercept of 1,109, and a correlation coefficient of 0.992. The line represents a satisfactory correlation between the two predicted values of form g IMC content. Thus NIR spectroscopy is an effective method for the evaluation to the pharmaceutical products of quantitative of polymorph.