• 대한기계학회:학술대회논문집
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• 대한기계학회 2000년도 춘계학술대회논문집B
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• pp.441-446
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• 2000

Chemical compositions of monodisperse $SiO_2/TiO_2$ multicomponent aggregates were measured for different heights from the burner surface and different mobility diameters of aggregates. $SiO_2/TiO_2$ multicomponent particles were generated in a hydrogen/oxygen coflow diffusion flame from two sets of precursors: TTIP (titanium tetraisopropoxide), TEOS(tetraethylorthosilicate). To maintain 1:1 mole ratio of TTIP:TEOS vapor theoretically, flow rate of carrier gas $N_2$ was fixed at 0.61pm for TTIP, at 0.11pm for TEOS. In situ sampling probe was used to supply particles into differential mobility analyzer(DMA) which was calibrated with using commercial DMA(TSI 3071A) and classifying monodisperse multicomponent particles. Classified particles were collected with electrophoretic collector. The distributions of composition from particle to particle were determined using EDS (energy dispersive spectrometry) coupled with TEM (transmission electron microscope). The chemical (atomic) compositions of classified monodisperse particle were obtained for different heights; z=40mm, 60mm, 80mm. The results suggested that the atomic composition of $SiO_2$ decreased with the height from burner surface and the composition of $SiO_2$ and $TiO_2$ approached to the value of 1 to 1 in far downstream. It is also found that the composition of $SiO_2$ decreases as the mobility diameter of aggregate increases.

• 대한치과기공학회지
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• 제43권4호
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• pp.145-152
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• 2021

Purpose: This study aimed to produce resin prosthetics using a dental barrel finishing machine. For dental resin grinding, the ingredients of the barrel finishing media were analyzed, and surface residues of the resin were observed. Methods: Two types of barrel finishing media for dental resin grinding were tested. Specimens were made from thermal polymerized, auto polymerized, and photopolymerized resins. Finishing media were analyzed through energy-dispersive X-ray spectroscopy (EDS) component analysis and inductively coupled plasma-optical emission spectrometry (ICP-OES) component analysis. Then, the prepared specimen was barrel finished for 25 minutes using two types of barrel finishing media, and scanning electron microscope was photographed to observe the surface residues. Results: As a result of EDS component analysis, both types of finishing media were analyzed for the components of C, O, Zr and Al elements, and industry media (IM) was further analyzed for the components of Si and Mg elements. In the ICP-OES component analysis, Cd and As, which are harmful elements, were detected in IM, and no harmful elements were detected in manufacturing media (MM). Because of observation of surface residues, no residues were observed in the three types of resin specimens that were barrel finished with two types of finishing media. Conclusion: Surface residue wasn't observed on the specimens polished using two types of finishing media. However, in IM, Cd and As, which are harmful elements, were detected, making it inappropriate for clinical use. In MM, harmful elements were not detected; therefore, clinical use will be possible.

• 한국식품과학회지
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• 제48권5호
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• pp.418-423
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• 2016

근적외선분광분석기와 에너지 분산형 X선 형광분석기를 이용한 분석방법을 개발하여 각각 97.5, 98.0%의 높은 정확도의 판별식을 확립하였고, 시중 유통 시료를 분석하여 검증한 결과 각각 96.3, 95.0%의 판별 정확도를 확인하였다. 이상의 연구 결과를 통하여 근적외선분광분석기와 에너지 분산형 X선 형광분석기를 이용하여 청국장 원산지 판별이 가능함을 확인하였고 이는 유기성분 함량에 따른 근적외선 흡광도와 무기성분 함량에 따른 X선 형광에너지 강도가 국내산과 수입산 간에 차이가 있기 때문으로 사료된다.

• 한국재료학회지
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• 제17권8호
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• pp.408-413
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• 2007

Process of the hydroxyapapite(HA) precipitation on bioactive titanium metal prepared by NaOH in a modified-simulated body fluid(mSBF) was investigated by high resolution transmission electron microscope (HRTEM) attached with energy dispersive X-ray spectrometer(EDX). The amorphous titanate phase on titanium surface is form by NaOH treatment and an amorphous titanate incorporated calcium and phosphate ions in the liquid to form an amorphous calcium phosphate. With increasing of soaking time in the liquid, the HA particles are observed in amorphous calcium phosphate phase with a Ca/P atomic ratio of I.30. The octacalcium phosphate (OCP) structure is not detected in HRTEM image and electron diffraction pattern. After a long soaking time, the HA particles grow as needle-like shape on titanium surface and a large particle-like aggregates of needle-like substance were observed to form on titanium surface within needle-like shape. A long axis of needle parallels to c-direction of the hexagonal HA structure.

• 한국식품과학회지
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• 제52권2호
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• pp.125-129
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• 2020

본 연구는 무기성분을 활용하여 국산 콩과 외국산 콩의 원산지 판별법을 개발하기 위해 수행하였다. 2018년도에 수집한 국산 100점, 미국, 중국, 베트남, 태국으로 구성된 외국산 97점에 대하여 ED-XRF를 이용하여 총 26종 무기성분의 농도를 산출하였다. T-test, ANOVA, CDA 분석을 통해 원산지판별에 영향을 주는 주요 변수로 5종(P, Ni, Br, Zn, Mn)의 무기성분을 선발하였다. 원산지 판별식을 설정한 결과 감응도 91.0%, 선택성 95.9%, 효율성 93.4%를 나타냈다. 2019년도에 수집한 국산 30점, 외국산 30점으로 원산지 판별식을 검증한 결과 국산 예측률 93.3%, 외국산 예측률 100.0%를 나타냈다. 복잡한 전처리 없이 ED-XRF와 통계처리를 통해 국산 콩과 외국산 콩을 판별할 수 있는 실용적인 판별 체계를 구축하였으며 부정유통 단속을 위한 과학적인 근거자료로서 활용이 가능할 것으로 판단된다.

• Corrosion Science and Technology
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• 제19권5호
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• pp.231-238
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• 2020

Radioactive corrosion product specimens were analyzed using an electron probe microanalyzer (EPMA) and X-ray image mapping. It is difficult to analyze the composition of radioactive corrosion products using an EPMA due to the size and rough shape of the surfaces. It is particularly challenging to analyze the composition of radioactive corrosion products in the form of piled up, small grains. However, useful results can be derived by applying a semi-quantitative analysis method using an EPMA with X-ray images. A standard-less, semi-quantitative method for wavelength dispersive spectrometry. EPMA analysis was developed with the objective of simplifying the analytical procedure required. In this study, we verified the reasonable theory of semi-quantitative analysis and observed the semi-quantitative results using a sample with a good surface condition. Based on the validated results, we analyzed highly rough-surface radioactive corrosion products and assessed their composition. Finally, the usefulness of the semi-quantitative analysis was reviewed by verifying the results of the analysis of radioactive corrosion products collected from spent nuclear fuel rods.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part 1
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• pp.338-339
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• 2006

The solubility of Cr in cubic carbides in the systems WC-Co-TaC and WC-Co-ZrC has been determined using equilibrium samples. Thermodynamic calculations were used to design the alloys through extrapolations of Gibbs energy expressions. The alloys were designed to have a microstructure containing the following phases: WC, liquid, $M_7C_3$, graphite and cubic carbide. The alloys were investigated using scanning electron microscopy and analyzed using energy-dispersive X-ray spectrometry. The present work shows how the Cr solubility depends on which cubic carbide former that is present. The WC-Co-Cr-Zr alloy has no detectable amount of Cr whereas the WC-Co-Cr-Ta alloy has 12% Cr in the cubic carbide.

• 한국분말재료학회지
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• 제8권1호
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• pp.42-49
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• 2001

Ti-50Ni(at%) and Ti-40Ni-10Cu(at%) alloy powders have been fabricated by ball milling method, and their microstructure and phase transformation behavior were investigated by means of scanning electron microscopy/energy dispersive spectrometry, differential scanning calorimetry (DSC), X-ray diffractions and transmission electron microscopy. In order to investigate the effect of ball milling conditions on transformation behavior, ball milling speed and time were varied. Ti-50Ni alloy powders fabricated with the milling speed more than 250 rpm were amorphous, while those done with the milling speed of 100rpm were crystalline. In contrast to Ti-50Ni alloy powders, Ti-40Ni-10Cu alloy powders were crystalline, irrespective of ball milling conditions. DSC peaks corresponding to martensitic transformation were almost discernable in alloy powders fabricated with the milling speed more than 250 rpm, while those were seen clearly in alloy powders fabricated with the milling speed of 100 rpm. This was attributed to the fact that a strain energy introduced during ball milling suppressed martensitic transformation.

• 임산에너지
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• 제21권3호
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• pp.18-27
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• 2002

소나무 수피를 유기 설폰산 촉매존재 하에서 페놀액화하고 얻어진 액화물에 대한 특성을 검토하였다. 수피의 페놀액화시 유기 설폰산은 염산보다 뛰어난 촉매임을 확인 할 수 있었으며, 본 촉매의 사용에 의하여 소나무 수피의 완전한 액화가 가능하였다. 이들 유기 설폰산을 촉매로하여 제조된 수피 액화물의 경우 액화용매로 사용된 페놀이 염산을 촉매로 한 경우에 비하여 2-3배 많이 결합해 있었으며, 유리 전이점(Tg)이 낮았다 (PTSA: 85℃, MSA: 169℃, HCI: 181℃). 또한 이들 액화물은 전수산기, 페놀성 수산기 및 지방족 수산기가 많이 존재하여 반응중 액화 용매인 페놀의 도입과 2차적인 축합억제를 예상할 수 있었다. 액화물의 IR 스펙트럼 및 중성당류 분석 결과로부터 수피 액화물 중의 탄수화물은 대부분 분해되었다는 것을 알 수 있었다. 액화물 및 그 잔사의 EDS 분석결과 유기 설폰산 촉매는 염산 촉매에 비하여 반응용기의 심각한 부식을 초래하지 않는다는 것을 알 수 있었다.

• 한국수소및신에너지학회논문집
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• 제31권3호
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• pp.276-283
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• 2020

Alcohol-based solvents including ethanol (EtOH) and tert-butyl alcohol (TBA) are investigated instead of isopropanol (IPA), which is a common solvent for polytetrafluoroethylene (PTFE), as an alternative solvent for preparing the catalyst slurry with PTFE binder. As a result, the performance at 0.2 A/㎠ from the single cells from using catalyst slurries based on EtOH and TBA showed very similar value to that from the slurry using IPA, which implies the EtOH and TBA can be used as a solvent for the catalyst slurry. It is also confirmed by the very close values of the total resistance of the membrane electrode assemblies from the slurries using different solvents. In the energy dispersive spectrometry (EDS) image, the shape of crack and dispersion of PTFE are changed according to the vapor pressure of the solvent.