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R.C 박스거교의 체계신뢰성 해석 및 안전도 평가 (Assessment of System Reliability and Capacity-Rating of Concrete Box-Girder Highway Brdiges)

  • 조효남;신재철
    • 콘크리트학회지
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    • 제7권3호
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    • pp.187-198
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    • 1995
  • 본 연구는 RC 박스거더교 상부구조의 체계신뢰성 해석과 체계신뢰성에 기초한 내하력 평가를 위하여 실용적이고 실제적인 신뢰성 모델 및 방법을 제안하였다. 시스템으로서 교량의 보유내하력을 정확히 예측한다는 것은, 특히 교량이 높은 여용성을 갖고 있고 열화손상이 심각한 경우에는 더욱 어려운 문제이다. 본 연구는 교량의 체계신뢰성에 상응하는 교량시스템강도로서 정의도리 수 잇는 등가의 시스템가동의 항으로 교량의 보유내하력을 평가하는 새로운 접근방법을 제안하였다. 즉, 이 방법은 체계신뢰성지수의 FOSM(Fdirst Order Second Moment)형태에서 유도된 등가시스템저항강도로서 보다 실제적이고 합리적인 극산시스템저항강도 평가방법이다. 본 연구에서 제안된 RC박스거더교를 위한 강도한계상태모형은 휨 및 전단강도에 기초하였다. 그리고 박스거더 상부구조의 체계신뢰성 문제는 주요 파괴 메카니즘이나 각거더의 한계파괴상태에 기초한 FMA(Failure Mode Approach) 로부터 획득한 직-병렬 혼합모델로서 정식화하였다. 제안된 모형의 신뢰성해석에는 AFOSM(Advanced First Order Second Moment) 과 IST(Importance Sampling Technique) 시뮬레이션 알고리즘을 사용하였다.

다양한 표면 처리 방법에 따른 비귀금속과 접착성 레진간의 결합력에 관한 연구 (A STUDY ON THE SHEAR BOND STRENGTH BETWEEN NONPRECIOUS METAL SURFACE AND RESIN CEMENT ACCORDING TO THE VARIOUS SURFACE TREATMENT METHODS)

  • 류형렬;임주환;조인호
    • 대한치과보철학회지
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    • 제39권2호
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    • pp.157-170
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    • 2001
  • The bond strength is the most important factor in establishing long-term success of resin-retained fixed prostheses. So, various surface treatment methods have been introduced to improve the bond strength of metal surface and bonding resin till now This study was performed to compare the effect of silicoating with that of metal primer and analyze the correlation between treatment time of sandblasting and the bond strength, so that meant to find more effective surface treatment method that could enhance the bond strength of resin-retained fixed prostheses. The surfaces of all specimens made of $Verabond^{(R)}$ alloys were air abraded with $250{\mu}m\;Al_2O_3$ according to treatment time of sandblasting and they were subdivided to be treated with only sandblasting(S group), silicoating following sandblasting(SS group) and metal primer application after sandblasting(SM group). Then pairs of metal specimens (${\phi}10mm{\times}h\;2mm,\;{\phi}6{\times}h\;2mm$) were bonded with Super bond $C&B^{(R)}$. The specimens were stored in $38^{\circ}C$ water for 48 hours and shear bond strength was measured using the universal testing machine. The results were as follows, 1. In the comparison of shear bond strength according to treatment time of sandblasting, bond strength was increased in the order of 0', 15', 30', 45', 60' group. 0' group had significantly lower value than any other, while 0', 15' group were significantly different with 30', 45', 60' group(p<0.05). 2. In the comparison of shear bond strength according surface treatment methods, bond strength was increased in the order of S group. SS group and SM group. S group was significantly different with SS group and SM group(p<0.05). 3. Observing the mode of bond failure. 0', 15' group showed only adhesive failure, and 30', 45', 60' group did mostly adhesive & cohesive failure in S group. In SS group and SM group, all other groups except 0', 15' group showed mostly cohesive failure. From the above results, it is considered that sandblasting should be treated for more than 30 seconds, and metal primer be more effective and available clinically than silicoater system which is complicate, technique-sensitive and time-consuming method, when nonprecious metal surface is planning be treated with in order enhance the bond strength of resin-retained fixed prostheses.

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MC-50 싸이클로트론을 이용한 $^{123}I$ 제법 연구 (The Development of Iodine-123 with MC-50 Cyclotron)

  • 서용섭;양승대;전권수;이종두;한현수
    • 대한핵의학회지
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    • 제25권2호
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    • pp.286-293
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    • 1991
  • $^{123}I$, which is applied for the thyroid and other in vivo kinetic study, has a special role in life sciences. The 159 KeV $\gamma-ray$ from $^{123}I$ is almost ideally appropriate for the current imaging instrumentation. Its decay mode (electron capture) and short half-life (13.3 hr) reduced the burden of radiation dose to the patients, and its chemical property makes it easy to synthesize the labelling compounds. In this experiment, the production of $^{123}I$ via the nuclear reaction $^{124}Te(p,2n)^{123}I$ with 28 MeV protons was sutdied. $TeO_2$ is used as a target material, because it has good physical properties. The target was prepared with $TeO_2$ powder and was molten into a ellipsoidal cavity (a=14 mm, b=10 mm, $270.8mg/cm^2$ thick) of pure platinum. The irradiation was carried out in the external proton beam with incident energies range from 28 MeV to 22 MeV, and current was $30{\mu}A$. The loss of $TeO_2$ target was significantly reduced by using $4\pi-cooling$ system in irradiation. The dry distillation method was adopted for the separation of $^{123}I$ from irradiated target, and when it was kept 5 minutes at $780^{\circ}C$, its result was quantitative. The loss of the target material $(TeO_2)$ was below 0.2% for each production run and $^{123}I$ from the dry distillation apparatus was captured with 0.01 N NaOH in $Na^{123}I$ form, then the pH of the solution was adjusted to $7.5\sim9.0$ with HC1/NaOH. The $Na^{123}I$ solution was passed through $0.2{\mu}m$ membrane filter, and sterilized under high pressure and temperature for 30 minutes. The production of $^{123}I$ is acceptable for clinical application based on the quality of USP XXI.

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LC-MS/MS를 이용한 수산물 중 콜리스틴 분석법 개발 (Development of Analytical Method for Colistin in Fish and Shrimp using Liquid Chromatography Mass Spectrometry)

  • 신다솜;강희승;이수빈;조윤제;천소영;정지윤;이규식
    • 한국식품위생안전성학회지
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    • 제31권5호
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    • pp.319-326
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    • 2016
  • LC-MS/MS를 이용하여 폴리펩타이드계 동물용의약품인 콜리스틴에 대한 시험법을 확립하여 정량성 및 정밀성을 확보하였으며, 확립된 시험법의 적용성 검증을 위해 국제식품규격위원회 기준에 따라 특이성, 정확성, 직선성, 정밀성, 검출한계, 정량한계 등을 검증하였다. 콜리스틴 표준용액을 잔류허용기준의 농도에 따라 검량선을 작성한 결과 0.99 이상의 직선성을 확인 할 수 있었으며, 본 실험에서의 평균 회수율은 85.9~107%이었다. 또한, 분석오차는 11.8% 이하로 정확성 및 재현성이 우수하였으며, 검출한계는 0.02 mg/kg, 정량한계는 0.05 mg/kg이었다. 또한, 실험실간 교차검증을 통하여 신뢰성을 확보하였다. 확립된 분석법은 양식 수산물 중 잔류할 수 있는 동물용의약품인 콜리스틴에 대한 안전관리에 활용 할 수 있을 것으로 판단된다.

Simultaneous Determination of Five Porphyrins in Human Urine and Plasma Using High Performance Liquid Chromatography-Tandem Mass Spectrometry

  • Hur, Yeoun;Tae, Sookil;Koh, Yun-Joo;Hong, Sung-Hyun;Yoon, Young Ho;Jang, Haejong;Kim, Sooji;Kim, Kyeong Ho;Kang, Seung Woo;Lee, Youngshin;Han, Sang Beom
    • Mass Spectrometry Letters
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    • 제5권2호
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    • pp.42-48
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    • 2014
  • A specific and sensitive liquid chromatography-electrospray ionization tandem mass spectrometry method (LC-ESI-MS/MS) was developed and validated for the simultaneous quantification of porphyrins (coproporphyrin, pentacarboxylporphyrin, hexacarboxylporphyrin, heptacarboxylporphyrin, and uroporphyrin) in human plasma and urine. Acidified plasma samples and urine samples were prepared by using liquid-liquid extraction using ethyl acetate and protein precipitation with acetonitrile, respectively. The separation was achieved onto a Synergi Fusion RP column ($150mm{\times}2.0mm$, $4{\mu}m$) with a gradient elution of mobile phase A (0.1% formic acid in 2 mmol/L ammonium acetate, v/v) and mobile phase B (20% methanol in acetonitrile, v/v) at a flow rate of $450{\mu}L$/min. Porphyrins and the internal standard (IS), coproporphyrin I-$^{15}N_4$, were detected by a tandem mass spectrometer equipped with an electrospray ion source operating in positive ion mode. Multiple reaction monitoring (MRM) transitions of the protonated precursor ions and the related product ions were optimized to increase selectivity and sensitivity. The proposed method was validated by assessing selectivity, linearity, limit of quantification (LOQ), precision, accuracy, recovery, and stability. The calibration curves were obtained in the range of 0.1-100 nmol/L and the LOQs were estimated as 0.1 nmol/L for all porphyrins. Results obtained from the validation study of porphyrins showed good accuracy, precision, recovery, and stability. Finally, the proposed method was successfully applied to clinical studies on the autism spectrum disorder (ASD) diagnosis of 203 Korean children.

Effects of variety, region and season on near infrared reflectance spectroscopic analysis of quality parameters in red wine grapes

  • Esler, Michael B.;Gishen, Mark;Francis, I.Leigh;Dambergs, Robert G.;Kambouris, Ambrosias;Cynkar, Wies U.;Boehm, David R.
    • 한국근적외분광분석학회:학술대회논문집
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    • 한국근적외분광분석학회 2001년도 NIR-2001
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    • pp.1523-1523
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    • 2001
  • The wine industry requires practical methods for objectively measuring the composition of both red wine grapes on the vine to determine optimal harvest time; and of freshly harvested grapes for efficient allocation to vinery process streams for particular red wine products, and to determine payment of contract grapegrowers. To be practical for industry application these methods must be rapid, inexpensive and accurate. In most cases this restricts the analyses available to measurement of TSS (total soluble solids, predominantly sugars) by refractometry and pH by electropotentiometry. These two parameters, however, do not provide a comprehensive compositional characterization for the purpose of winemaking. The concentration of anthocyanin pigment in red wine grapes is an accepted indicator of potential wine quality and price. However, routine analysis for total anthocyanins is not considered as a practical option by the wider wine industry because of the high cost and slow turnaround time of this multi-step wet chemical laboratory analysis. Recent work by this ${group}^{l,2}$ has established the capability of near infrared (NIR) spectroscopy to provide rapid, accurate and simultaneous measurement of total anthocyanins, TSS and pH in red wine grapes. The analyses may be carried out equally well using either research grade scanning spectrometers or much simpler reduced spectral range portable diode-array based instrumentation. We have recently expanded on this work by collecting thousands of red wine grape samples in Australia. The sample set spans two vintages (1999 and 2000), five distinct geographical winegrowing regions and three main red wine grape varieties used in Australia (Cabernet Sauvignon, Shiraz and Merlot). Homogenized grape samples were scanned in diffuse reflectance mode on a FOSE NIR Systems6500 spectrometer and subject to laboratory analysis by the traditional methods for total anthocyanins, TSS and pH. We report here an analysis of the correlations between the NIR spectra and the laboratory data using standard chemometric algorithms within The Unscrambler software package. In particular, various subsets of the total data set are considered in turn to elucidate the effects of vintage, geographical area and grape variety on the measurement of grape composition by NIR spectroscopy. The relative ability of discrete calibrations to predict within and across these differences is considered. The results are then used to propose an optimal calibration strategy for red wine grape analysis.

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Wine quality grading by near infrared spectroscopy.

  • Dambergs, Robert G.;Kambouris, Ambrosias;Schumacher, Nathan;Francis, I. Leigh;Esler, Michael B.;Gishen, Mark
    • 한국근적외분광분석학회:학술대회논문집
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    • 한국근적외분광분석학회 2001년도 NIR-2001
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    • pp.1253-1253
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    • 2001
  • The ability to accurately assess wine quality is important during the wine making process, particularly when allocating batches of wines to styles determined by consumer requirements. Grape payments are often determined by the quality category of the wine that is produced from them. Wine quality, in terms of sensory characteristics, is normally a subjective measure, performed by experienced winemakers, wine competition judges or winetasting panellists. By nature, such assessments can be biased by individual preferences and may be subject to day-to-day variation. Taste and aroma compounds are often present in concentrations below the detection limit of near infrared (NIR) spectroscopy but the more abundant organic compounds offer potential for objective quality grading by this technique. Samples were drawn from one of Australia's major wine shows and from BRL Hardy's post-vintage wine quality allocation tastings. The samples were scanned in transmission mode with a FOSS NIR Systems 6500, over the wavelength range 400-2500 ㎚. Data analysis was performed with the Vision chemometrics package. With samples from the allocation tastings, the best correlations between NIR spectra and tasting data were obtained with dry red wines. These calibrations used loadings in the wavelengths related to anthocyanins, ethanol and possibly tannins. Anthocyanins are a group of compounds responsible for colour in red wines - restricting the wavelengths to those relating to anthocyanins produced calibrations of similar accuracy to those using the full wavelength range. This was particularly marked with Merlot, a variety that tends to have relatively lower anthocyanin levels than Cabernet Sauvignon and Shiraz. For dry white wines, calibrations appeared to be more dependent on ethanol characteristics of the spectrum, implying that quality correlated with fruit maturity. The correlations between NIR spectra and sensory data obtained using the wine show samples were less significant in general. This may be related to the fact that within most classes in the show, the samples may span vintages, glowing areas and winemaking styles, even though they may be made from only one grape variety. For dry red wines, the best calibrations were obtained with a class of Pinot Noir - a variety that tends to be produced in limited areas in Australia and would represent the least matrix variation. Good correlations were obtained with a tawny port class - these wines are sweet, fortified wines, that are aged for long periods in wooden barrels. During the ageing process Maillard browning compounds are formed and the water is lost through the barrels in preference to ethanol, producing “concentrated” darkly coloured wines with high alcohol content. These calibrations indicated heaviest loadings in the water regions of the spectrum, suggesting that “concentration” of the wines was important, whilst the visible and alcohol regions of the spectrum also featured as important factors. NIR calibrations based on sensory scores will always be difficult to obtain due to variation between individual winetasters. Nevertheless, these results warrant further investigation and may provide valuable Insight into the main parameters affecting wine quality.

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수산물 중 네오마이신, 겐타마이신 동시분석법 개발 (Simultaneous Analytical Method for the Neomycin, Gentamicin Residues in Seafood)

  • 홍영민;이석기;김형아;황유경
    • Journal of Applied Biological Chemistry
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    • 제53권1호
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    • pp.25-30
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    • 2010
  • 선진 각국에서는 항생제 등 동물용의약품의 사용을 엄격하게 규제하고 있으며, 식품 중 동물용의약품의 잔류허용기준(Maximum Residue Levels, MRLs)을 설정하여 과다한 사용을 억제토록 정책을 유지하고 있다. 우리나라에서도 CODEX 기준을 바탕으로 식품 중 동물용의약품에 대한 MRLs 및 시험방법을 설정하여 식품공전에 제시하고 있으며 HPLC, LC/MS/MS 또는 GC/MS 등 기기의 발달, 분석법의 개발 등으로 기존의 시험법을 대체하거나 효율적인 시험법을 확립함으로써 지속적인 시험법의 개발, 개선향상 및 관리로 안전한 식품관리의 신뢰성 확보가 요구되고 있다. 본 연구에서는 기존의 HPLC/UVD나 유도체화 분석 등을 통해 검출이 어려운 네오마이신과 겐타마이신에 대해 LC/MS를 이용한 동시분석방법을 검토하였으며, 몇 가지 수산물 검체에 대한 적용성을 평가하였다. 대상 수산물은 광어, 우럭, 장어, 대하 등 4종이었으며 전처리 방법으로 추출용매는 2% 아세트산을 함유한 20% 아세토나이트릴과 HLB 카트리지와 WCX 카트리지를 연결하여 사용하였다. LC/MS 동시분석 조건은 이동상으로 용매 A: 5 mM heptafluorobutyric acid, 용매 B: 아세토나이트릴을 이용하여 gradient로 유속은 0.4 mL/min로 하였다. 그 결과, 각 정량기준농도의 0.5, 1, 2, 4배 농도에서 검량선의 직선성($r^2$)은 네오마이신 0.989, 겐타마이신 0.989이었으며 네오마이신의 회수율과 CV는 0.25~1.00 mg/kg에서 각각 92~115% 및 1.3~5.6%, 각 수산물에 대한 LOD와 LOQ는 각각 0.0005~0.0007 mg/kg 및 0.0017~0.0023 mg/kg이었다. 겐타마이신의 회수율과 CV는 0.05~0.20 mg/kg에서 각각 99~116% 및 3.0~22.1%, 각 수산물에 대한 LOD와 LOQ는 각각 0.0017~0.0100 mg/kg 및 0.0056~0.0333 mg/kg이었다. 향후 이들 수산물에 대한 대상 동물용의약품의 MRLs 설정 시 활용할 수 있을 것으로 판단된다.

적외선 살균이 고춧가루의 품질에 미치는 영향 (Effects of Infrared Pasteurization on Quality of Red Pepper Powder)

  • 정진주;최은주;이유진;강성태
    • 한국식품과학회지
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    • 제43권2호
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    • pp.156-160
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    • 2011
  • 고춧가루의 살균을 위하여 이송판 상부와 하부에 각각 총 4개의 적외선램프(총출력 8000 W)와 온수순환장치를 장착하고 진동장치를 사용해 분체를 이송하는 분체살균장치를 제작하였다. 진균은 2000 W 이상의 적외선 출력에서 대한 완전살균이 가능하였다. 그러나 일반세균수는 유의적으로 감소하지는 아니하였다. 고춧가루 중 미생물의 효과적인 살균과 수분함량의 감소를 줄이기 위한 고춧가루의 최적 이동속도는 106-164 g/min 범위로 확인되었다. 고춧가루의 입자크기와 무관하게 진균을 완전히 살균할 수 있었으며 수분 함량은 9 mesh보다는 32 mesh의 고운 고춧가루가 더 높은 수분함량의 감소를 보여 주었다. 고춧가루에 대한 반복된 적외선 살균은 고춧가루의 수분함량(초기 12.6%)의 급속한 감소(2회 살균 후 4.6%)로 인하여 바람직하지 아니하였다. 1회 살균만으로도 진균은 불검출 되었으며 살균 횟수가 증가할수록 수분함량이 감소하였다. 한편 적외선살균 후 고춧가루의 총 capsaicinoid의 함량과 ASTA 색도, 표면색도는 모든 살균 조건에서 살균전과 비교하여 유의적인 차이를 보이지 않았다.

비차폐 환경에서의 고온초전도 SQUID 2차 미분기의 특성연구 (High-$T_c$ 2nd-order SQUID Gradiometer for Use in Unshielded Environments)

  • 박승문;강찬석;이순걸;유권규;김인선;박용기
    • Progress in Superconductivity
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    • 제5권1호
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    • pp.50-54
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    • 2003
  • We have fabricated $∂^2$$B_{z}$ /$∂x^2$ type planar gradiometers and studied their properties in operation under various field conditions. $YBa_2$$Cu_3$$O_{7}$ film was deposited on $SrTiO_3$ (100) substrate by a pulsed laser deposition (PLD) system and patterned into a device by the photolithography with ion milling technique. The device consists of 3 pickup loops designed symmetrically Inner dimension and the width of the square side loops are 3.6 mm and 1.2 mm, respectively, and the corresponding dimensions of the center loop are 2.0 mm and 1.13 mm. The length of baseline gradiometer is 5.8 mm. Step-edge junction width is 3.0 $\mu\textrm{m}$ and the hole size of the SQUID loop is 3 $\mu\textrm{m}$ ${\times}$ 52 $\mu\textrm{m}$. The SQUID inductance is estimated to be 35 pH. The device was formed on a 20 mm ${\times}$ 10 mm substrate. We have tested the behavior of the device in various field conditions. The unshielded gradiometer was stable under extremely hostile conditions on a laboratory bench. Noise level 0.45 pT/$\textrm{cm}^2$/(equation omitted)Hz and 0.84 pT/$\textrm{cm}^2$/(equation omitted)Hz at 1 Hz for the shielded and the unshielded cases, which correspond to equivalent field noises of 150 fT/(equation omitted)Hz and 280 fT/(equation omitted)Hz, respectively. In spite of the short baseline of 5.8 mm, the high common-mode-rejection-ratio of the gradiometer, $10^3$, allowed us to successfully record magnetocardiogram of a human subject, which demonstrates the feasibility of the design in biomagnetic studies.

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