• 제목/요약/키워드: SEM EDAX

검색결과 88건 처리시간 0.023초

Ferrography에서 샘풀희석률이 마모입자 정량분석에 미치는 영향 (The Effect of Dilution on Porticle Deposition in The Entry Deposit of The Ferrogroms)

  • 권오관
    • Tribology and Lubricants
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    • 제1권1호
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    • pp.38-45
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    • 1985
  • Ferrography 방법은 유체중 마모입자를 Substrate glass 위에 Van der Waals 힘에 의하여 분산교착 시키므로써 윤활 Systems에서의 기계요소들의 동특성적 마모진행과정및 mechanism의 정성적및 정량적인 분석을 가능케 한다. 정성적 방법으로는 광학현미경으로부터 SEM, X-Ray Emissiom, EDAX등의 분석방법이 적용되고 있으나, 정량적으로는 마모입자의 크기별 분포함수에 따른 Variance, Kurtosis, Skewness와 같은 인자함수의 변이가 마모진행 과정과 진행될 마모형태기구의 예측인자로서 연구되고 있다. 수치적 Model로 마모진행기구를 예측할 경우 third moment의 Skewness 가 Size 및 number분포에 따라 예민하게 반응을 나타내는 결과를 보이고 있다. 이러한 정량분석을 위하여는 실험 Sample에 따라서, 즉 오염도에 따른 Sample희석이 따르는데, 이러한 Sample 희석이 정량적 분포에 미치는 영향에 관한 연구결과는 아직 없다. 따라서 본연구에는 용제희석이 정량적 마모입자 분포에 미치는 영향을 image analyser인 Quantimat 720을 이용하여 검토하였으며 전영역의 희석률에 적용될 수 있는 Standard Calibration function에 따른 수학적 model을 유도하였다.

가시광감응을 위한 금속이나 $WO_3$ 도핑된 $TiO_2$ 튜브의 광활성 연구 (Photocatalytic activity under visible-light with metal or $WO_3$ deposited-$TiO_2$ tubes)

  • 허아영;이창하;박민성;심은정;윤재경;주현규
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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    • pp.227.1-227.1
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    • 2010
  • 본 연구는 자외선 영역의 흡수로 전자 정공의 전하쌍을 생성함으로써 광전압 및 전류를 일으키는 티타니아 물질을 금속지지체 표면에 양극산화로 튜브형 $TiO_2$(anodized tubular $TiO_2$; ATT)로 제조한 후 나노크기의 금속 혹은 $WO_3$입자를 담지하여 광감응 재료로 활용하였다. 이는 기존의 입자나 콜로이드 형태로 광촉매 물질을 고정화하여 사용한 재료의 탈리현상 및 효율저하를 극복하기 위함이다. ATT는 전해질 내에 전기화학적 에칭율과 화학적 용해율의 비율에 의해 나노튜브 길이 성장에 영향을 미치는데 이를 유기 전해질과 불산 전해질을 사용하여 정전압 혹은 정전류의 조건에서 다양한 길이의 $TiO_2$ 나노튜브를 제조하였다. 여기에 전기분해담지(electrolytic deposition; ELD)를 통하여 정전류 조건에서 다양한 금속(Pt, Pd, Ru)을 나노크기의 형태로 담지하여 광촉매 내 생성된 전자 정공의 재결합을 줄이고자 하였고 $WO_3$의 담지를 통하여 가시광 감응을 높이고자 하였다. 제조된 여러 조건의 시료는 SEM과 EDAX를 통하여 형태와 길이, 담지량을 확인 하고 XRD를 이용하여 열처리 온도에 따른 결정화상태를 확인하였으며 광전류 측정 및 Cr(VI)의 광환원과 MB의 광분해를 통하여 광효율을 관찰하였다. 금속이 도핑되었을 경우 순수 ATT보다 보통 3배의 흡착률과 UV광원 아래 2배의 광효율을 관찰할 수 있었는데 이 중 Pt의 담지가 가장 효율이 좋았으며 흡착률에서는 담지량의 증가에 따른 증가선을 관찰 할 수 있었으나 광원 사용시 3%담지율에서 최적을 확인 할 수 있었다. 또한 $TiO_2$외 가시광감응 활성을 높이기 위한 다양한 광촉매제조가 진행 중에 있다.

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열처리에 의한 도재용 Ni-Cr합금 표면의 변화에 관한 연구 (METAL SURFACE CHANGES BY HEAT TREATMENT OF Ni-Cr ALLOYS)

  • 김영한;이선형;양재호;정헌영
    • 대한치과보철학회지
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    • 제27권2호
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    • pp.219-248
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    • 1989
  • The purposes of this study were to analyze the microstructural and compositional changes of metal surfaces following different conditions of preoxidizing heat treatment, to investigate the composition of metal oxides, and to evaluate the effect of preoxidation and removal of surface oxides on microstructure and diffusion profiles. The techniques of EDAX (energy-dispersive analysis of x-ray), ESCA (electron spectroscopy for chemical analysis), and EPMA (electron probe micro analysis) were used, along with SEM (scanning electron microscopy). The obtained results were as follows : 1. A surface of the specimen became rough and the amount of the metal oxides increased with increasing the heat treatment time and temperature and the partial pressure of oxygen. 2. At an air pressure of 28' vacuum, the higher the temperature and the longer the time of preoxidation, the higher Ni concentration was detected. 3. Cr concentration in the specimen heat treated with air was higher than that of with vacuum. 4. The oxides in the specimens were mainly composed of Ni and Cr oxides. On the globular growth particles, significant rises in Al concentration of Rexillium III and Ti concentration of Verabond were noted. 5. Atomic diffusion occurred at the ceramic-metal interface, furthermore the amount of the flux was increased with preoxidation heat treatment.

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$CdS/CuInSe_2$태양전지의 Window Layer로 쓰이는 CdS박막의 진공증착법에 따른 전기적.광학적 성질 (Electrical and Optical Properties of Vacuum-Evaporated CdS Films for the Window Layer of $CdS/CuInSe_2$ Solar Cells.)

  • 남희동;이병하;박성
    • 한국결정학회지
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    • 제8권2호
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    • pp.105-110
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    • 1997
  • CdS/CuInSe2 태양전지에서 창측재료로 1μm 두께의 CdS박막을 1x10-3mTorr의 진공하에서 CdS source 온도를 800-1100'C로 하고 기판의 온도를 50-200℃로하여 진공증차겁으로 제조하였다. 증착된 CdS박막의 구조적, 전기적, 광학적 특성조사는 x-ray diffractometer(XRD), scanning electron microscope(SEM), 전기비저항 측정, Hall measurement 그리고 optical transmission spectra로 행하였고, 각막들의 성분분석은 energy dispersive analysis of X-ray (EDAX)를 가하나, 광투과도는 감소하였다. 이때 증착된 CdS 박막들은 모두 hexagonal 구조를 가지고 있었으며, 결정성은 기판유리를 딸 (002)면으로 형성되었다. CdS Source 온도가 1000℃에서 증착된 CdS 박막이 0.9(S/cm)의 가장 높은 전기 전도도를 나타내었다. 또한 기판온도를 100'C로 제조한 CdS 박막이 전기비저항은 40(Ω,cm)이었고 광투과도는 80% 이상의 값을 나타내어 CdS/CuInSe2 태양전지의 창측재료로 적합했다.

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친환경 재료를 사용한 흑색 지르코니아 세라믹스 제조 (Manufacture of Black Color Zirconia Ceramics Used by Eco-Friendly Materials)

  • 주인돈;이병하
    • 한국재료학회지
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    • 제21권12호
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    • pp.685-689
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    • 2011
  • The goal of this investigation was to produce a zirconia-family black ceramics that has enhanced functionality and reliability. Color zirconia ceramics have been produced by adding pigments. Pigments cause structural defects within zirconia and result in a drop in physical properties. Using environmentally friendly rice husk, we produced a black zirconia that is free of structural defects. In optimal firing conditions for black zirconia the calcining temperatures of the molding product are changed from $400^{\circ}C$ to $1200^{\circ}C$, and the firing temperatures are changed from $1400^{\circ}C$ to $1600^{\circ}C$. Color of testing the specimens was analyzed using Ultraviolet (UV) spectroscopy. Scanning Electron Microscope (SEM), EDAX (EDX), and Fourier transform infrared spectroscopy (FT-IR) analyses were carried out in order to examine impregnation properties and crystal phases. Universial Test Machine (UTM) was used to measure the flexual strength as well as the compressive strength. From experimental results, it was found that in optimal firing conditions the sample was calcined from $1000^{\circ}C$ to $1500^{\circ}C$. Commission internationalde I'Edairage (CIE) values of manufactured black zirconia color were $L^*$ = 29.73, $a^*$ = 0.23, $b^*$ = -2.68. The bending strength was 918 MPa and the compressive strength was 2676 MPa. These strength values are similar to typical strength values of zirconia, which confirms that carbon impregnation did not influence physical properties.

Preparation of chitosan, sunflower and nano-iron based core shell and its use in dye removal

  • Turgut, Esra;Alayli, Azize;Nadaroglu, Hayrunnisa
    • Advances in environmental research
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    • 제9권2호
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    • pp.135-150
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    • 2020
  • Many industries, such as textiles, chemical refineries, leather, plastics and paper, use different dyes in various process steps. At the same time, these industrial sectors are responsible for discharging contaminants that are harmful and toxic to humans and microorganisms by introducing synthetic dyes into wastewater. Of these dyes, methylene blue dye, which is classified as basic dyes, is accepted as a model dye. For this reason, methylene blue dye was selected in the study and its removal from the water was studied. In this study, two efficient biosorbents were developed from chitosan and sunflower waste, an agro-industrial waste and modified using iron nanoparticles. The biosorption efficiency was evaluated for methylene blue (MB) dye removal from aqueous solution under various parameters such as treating agent, solution pH, biosorbent dosage, contact time, initial dye concentration and temperature. We investigated the kinetic properties of dye removal from water for Chitosan-Sunflower (CS), Chitosan-Sunflower-Nanoiron (CSN). When the wavelength of MB dye was spectrophotometrically scanned, the maximum absorbance was determined as 660 nm. For the core shell biosorbents we obtained, we found that the optimum time for removal of MB from wastewater was 60 min. The pH of the best pH was determined as 5 in the studied pH. The most suitable temperature for the experiment was determined as 30℃. SEM-EDAX, TEM, XRD, and FTIR techniques were used to characterize biosorbents produced and modified in the experimental stage and to monitor the change of biosorbent after dye removal. The interactions of the paint with the surface used for removal were explained by these techniques. It was calculated that 80% of CS and 88% of CSN removed MB in optimum conditions. Also, the absorption of MB dye onto the surface was investigated by Langmiur and Frendlinch isotherms and it was determined from the results that the removal was more compatible with Langmiur isotherm.

X-ray / gamma ray radiation shielding properties of α-Bi2O3 synthesized by low temperature solution combustion method

  • Reddy, B. Chinnappa;Manjunatha, H.C.;Vidya, Y.S.;Sridhar, K.N.;Pasha, U. Mahaboob;Seenappa, L.;Sadashivamurthy, B.;Dhananjaya, N.;Sathish, K.V.;Gupta, P.S. Damodara
    • Nuclear Engineering and Technology
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    • 제54권3호
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    • pp.1062-1070
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    • 2022
  • In the present communication, pure and stable α-Bismuth Oxide (Bi2O3) nanoparticles (NPs) were synthesized by low temperature solution combustion method using urea as a fuel and calcined at 500℃. The synthesized sample was characterized by using powder X-ray Diffraction (PXRD), Scanning Electron Microscopy (SEM), Energy dispersive X-ray analysis (EDAX), Transmission Electron Microscopy (TEM), Fourier Transform Infrared Spectroscopy (FTIR) and UV-Visible absorption spectroscopy. The PXRD pattern confirms the formation of mono-clinic, stable and low temperature phase α-Bi2O3. The direct optical energy band gap was estimated by using Wood and Tauc's relation which was found to be 2.81 eV. The characterized sample was studied for X-ray/gamma ray shielding properties in the energy range 0.081-1.332 MeV using NaI (Tl) detector and multi channel analyzer (MCA). The measured shielding parameters agrees well with the theory, whereas, slight deviation up to 20% is observed below 356 keV. This deviation is mainly due to the influence of atomic size of the target medium. Furthermore an accurate theory is necessary to explain the interaction of X-ray/gamma ray with the NPs.The present work opens new window to use this facile, economical, efficient, low temperature method to synthesize nanomaterials for X-ray/gamma ray shielding purpose.

고정층 반응기에서 K-계열 흡수제의 압력에 따른 HCl 흡수 거동 연구 (Effect of Pressure on HCl Absorption Behaviors of a K-based Absorbent in the Fixed Bed Reactor)

  • 김재영;박영철;조성호;류호정;백점인;박영성;문종호
    • 청정기술
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    • 제19권2호
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    • pp.165-172
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    • 2013
  • 본 연구에서는 고정층 반응기(높이 15 cm, 내경 0.5 cm)에서 K-계열 건식 흡수제($K_2CO_3/Al_2O_3$, 한국전력공사 전력연구원)를 이용하여 반응압력 변화에 따른 염화수소 흡수 실험을 수행하였다. 반응온도는 가스화 직후, 필터를 거쳐서 주입되는 것을 가정하여 $400^{\circ}C$로 설정하였으며, 반응기체 농도는 750 ppm HCl ($N_2$ balance)으로 설정하였다. 반응압력은 1, 5, 10, 15, 20 bar로 증가시켰다. 압력이 증가할수록 K-계열 흡수제의 흡수 성능이 증가하였다. 흡수제를 구성하고 있는 주요 물질인 $K_2CO_3$가 HCl 가스와 반응하여 KCl 결정을 형성하였으며, 강한 결합에너지로 인하여 흡수제의 재생이 실질적으로 불가능하였다. 이에 대한 광학적, 물리적, 화학적 특성을 SEM, EDX, BET, TGA, XRD를 이용하여 분석하였다. $400^{\circ}C$, 20 bar 조건(가스화 이후 탈할로겐 공정의 온도 및 압력조건)에서 $K_2CO_3$ 흡수제는 Ca 계열 및 Mg 계열의 흡수제에 비해 높은 HCl 흡수능 및 HCl/$N_2$ 분리 거동을 보였다.

칼슘수용액으로 처리한 상아질과 합착용 글래스아이오노머의 전단결합강도에 관한 연구 (A STUDY ON THE SHEAR BOND STRENGTH OF LUTING GLASS IONOMER AND DENTIN TREATED WITH CALCIUM SOLUTION)

  • 백영걸;이성복;박남수
    • 대한치과보철학회지
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    • 제34권3호
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    • pp.593-610
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    • 1996
  • The objective of this paper was to evaluate the shear bond strength of luting glass ionomer cement with defferent calcium based solution treatment on dentin surface. 120 extracted human teeth were classified into 12 group based on presence of smear layer on dentin surface and type of treatment solution. Smear layer remove on dentin surface was done using 6% citric acid for 60 seconds. Five different dentin surface treatment solutions(calcium acetate, calcium carbonate, clacium chlorided, calcium hydroxide, and calcium phosphate) were evaluated in this study. After surface modification, metal ring(inner diameter : 3mm, depth : 1mm) was placed to expose the same dentin surface area and inner space was filled with luting glass ionomer cement according to the recommended procedure for stadard clinical procedure. The shear bond strength of glass ionomer cement was determined after 24 hours. SEM was used for the evaluation of the surface morphologic changes and EDAX analysis was done for determination of the change of the calcium contents of treated dentin. Follwing conclusion can be drawn : 1. In the group of the dentin surface with smear layer, the calcium carbonate solution was the most effective for the increase of the clacium content and the shear bond strength of glass ionomer cement to dentin surfaces. 2. In the group of the calcium carbonate treated dentin with msear layer, the shear bond strength was increased twice compared to the control group and cohesive failure mode was observed. 3. The shear bond strength of cement was increased significantly be the removal of smear layer using 6% citric aicd. However, additional calcium solution treatments were not effective for further bond strength increase. 4. The shear bond strength of cement was significantly improved by both of the removal of smear layer and the calcium solution treatment, and the former was more effective for bond strength improvement. 5. The smear layer removed/calcium solution treated groups showed dentinal tubule obstruction and crystal attachment in SEM evaluation. However, the shear bond strengths of these groups were not increased compared to the smear layer removed/no dentin treatment group.

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탈회된 법랑질에서 CPP-ACP의 재광화 깊이 (REMINERALIZATION DEPTH OF CPP-ACP ON DEMINERALIZATION HUMAN ENAMEL IN VITRO)

  • 최한주;최영철;김광철;최성철
    • 대한소아치과학회지
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    • 제35권2호
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    • pp.278-286
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    • 2008
  • 이 연구는 Casein phosphopeptides-amorphous calcium phosphate (CPP-ACP)paste에 의해 제공되는 Calcium(Ca)과 Phosphorous(P) 이온이 탈회된 법랑질 표면에 적용된 시간에 따라 침투되는 깊이와 Ca/P의 상대적 정량값을 평가하고자 하였다. Field Emission Scanning Electron Microscopy(FE-SEM)와 Energy Dispersive X-ray Spectrometer(EDS)를 이용하여 Ca/P 이온의 정량적 측정으로 탈회된 법랑질 내로의 침투깊이를 계측하였다. 교정치료를 위해 발거된 제 1소구치 치관 협측면의 중앙 1/3부위에 $4{\times}9mm$의 법랑질 window를 제외한 나머지 치관부위는 nail varnish로 도포하여 window 부위의 법랑질만 노출시킨 후, 모든 치아를 0.1M lactic acid로 7일 동안 탈회시켰다. 탈회된 각 치아의 정중앙을 장축에 따라 절단한 후 그 중 4개의 소구치 절편은 10배 희석된 CPP-ACP paste 용액에 각각 1, 2, 3 및 5주 동안 침지시켰고, 나머지 4개의 소구치 절편은 증류수에 동일 기간 침지시켰다. 각 절편을 window에 대해 수직으로 절단하여 건전 법랑질, 탈회된 법랑질 및 재광화된 법랑질의 깊이에 따른 Ca/P의 Spectrum Density Index(SDI)를 FE-SEM과 EDS로 계측하였다. 각 계측치를 Student's t test로 비교 평가하여 다음과 같은 결과를 얻었다. 1. Ca/P 이온이 법랑질 표면으로부터 약 $1050{\sim}1400{\mu}m$까지 침투하여 탈회 법랑질의 깊이인 $1050{\sim}1350{\mu}m$까지 재 광화되었다. 2. 1주군과 2주군의 재광화된 법랑질의 Ca/P SDI는 건전 법랑질보다 유의성 있게 높았으나(p<0.05), 3주군에서는 건전 법랑질보다 유의하게 낮았고(p<0.05), 5주군은 건전 법랑질과 유의한 차이가 없었다(p>0.05). 3. 모든 재광화된 법랑질 간에 Ca/P의 SDI는 유의한 차이가 없었다(p>0.05).

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