• 제목/요약/키워드: Range limits

검색결과 753건 처리시간 0.028초

핫스탬핑 공정에서 Tailor Rolled Blank 의 성형 특성을 고려한 성형한계 예측 (Limits Considering the Deformation Characteristics of Tailor Rolled Blank during Hot Stamping)

  • 김재홍;고대훈;서판기;김병민
    • 소성∙가공
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    • 제23권6호
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    • pp.351-356
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    • 2014
  • The current study aims to predict the forming limits considering the deformation characteristics of tailor rolled blank(TRB) during hot stamping. The formability of TRB is affected by the TRB line orientation because elongations change due to the intrinsic geometry within the sheet. To evaluate the forming limits, Nakazima tests were conducted at elevated temperatures with different TRB line orientations. Forming limit diagrams(FLD) of TRB can be predicted by an interpolating equation based on the Nakazima test. Predicted FLDs were used in FE-simulations of a rectangular drawing. The predicted limit drawing height was compared with experimental results. The simulation results show good agreement with the experimental ones with an error range of 3%.

정지궤도위성과 발사체와의 전자파 적합성 해석 (Preliminary EMC Analysis between the COMS and the Arian V Launch Vehicles)

  • 김의찬;이흥호
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2008년도 제39회 하계학술대회
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    • pp.1403-1405
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    • 2008
  • In this paper, the preliminary EMC analysis process between the Communication, Ocean and Meteorological Satellite (COMS) and Geostationary Earth Orbit (GEO) launch vehicles in the frequency range [1MHz-47MHz] is described. The considered launch vehicle is the Arian V. The launch vehicle Radiated Emission (RE) specifications have been compared to COMS satellite Radiated Susceptibility (RS) limits. The COMS RS limits are the RS qualification levels of COMS units during launch. As a result, The radiated emission levels of the Arian V is compliant with COMS RS limits.

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Simultaneous Determination and Occurrences of Pharmaceuticals by Solid-Phase Extraction and Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) in Environmental Aqueous Samples

  • Koo, So-Hyun;Jo, Cheon-Ho;Shin, Sun-Kyoung;Myung, Seung-Woon
    • Bulletin of the Korean Chemical Society
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    • 제31권5호
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    • pp.1192-1198
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    • 2010
  • Pharmaceuticals and personal care products (PPCPs) are emerging contaminants in the aquatic environment. Many pharmaceuticals are not completely removed during wastewater treatment, leading to their presence in wastewater treatment effluents, rivers, lakes, and ground water. Here, we developed analytical methods for monitoring ten pharmaceuticals from surface water by LC/ESI-MS/MS. For sample clean-up and extraction, MCX (mixed cation exchange) and HLB (hydrophilic-lipophilic balance) solid-phase extraction (SPE) cartridges were used. The limits of detection (LOD) in distilled water and the blank surface water were in the range of 0.006 - 0.65 and 1.66 - 45.05 pg/mL, respectively. The limits of quantitation (LOQ) for the distilled water and the blank surface water were in the range of 0.02 - 2.17 and 5.52 - 150.15 pg/mL, respectively. The absolute recoveries for fortified water samples were between 62.1% and 125.4%. Intra-day precision and accuracy for the blank surface water were 2.9% - 24.1% (R.S.D.) and -16.3% - 16.3% (bias), respectively. In surface wastewater near rivers, chlortetracycline and acetylsalicylic acid were detected frequently in the range of 0.017 - 5.404 and 0.029 - 0.269 ng/mL, respectively. Surface water near rivers had higher levels than surface water of domestic treatment plants.

Elevational distribution ranges of vascular plant species in the Baekdudaegan mountain range, South Korea

  • Shin, Sookyung;Kim, Jung-Hyun;Dang, Ji-Hee;Seo, In-Soon;Lee, Byoung Yoon
    • Journal of Ecology and Environment
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    • 제45권1호
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    • pp.62-71
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    • 2021
  • The climate is changing rapidly, and this may pose a major threat to global biodiversity. One of the most distinctive consequences of climate change is the poleward and/or upward shift of species distribution ranges associated with increasing temperatures, resulting in a change of species composition and community structure in the forest ecosystems. The Baekdudaegan mountain range connects most forests from the lowland to the subalpine zone in South Korea and is therefore recognized as one of the most important biodiversity hotspots. This study was conducted to understand the distribution range of vascular plants along elevational gradients through field surveys in the six national parks of the Baekdudaegan mountain range. We identified the upper and lower distribution limits of a total of 873 taxa of vascular plants with 117 families, 418 genera, 793 species, 14 subspecies, 62 varieties, two forms, and two hybrids. A total of 12 conifers were recorded along the elevational gradient. The distribution ranges of Abies koreana, Picea jezoensis, Pinus pumila, and Thuja koraiensis were limited to over 1000 m above sea level. We also identified 21 broad-leaved trees in the subalpine zone. A total of 45 Korean endemic plant species were observed, and of these, 15 taxa (including Aconitum chiisanense and Hanabusaya asiatica) showed a narrow distribution range in the subalpine zone. Our study provides valuable information on the current elevational distribution ranges of vascular plants in the six national parks of South Korea, which could serve as a baseline for vertical shifts under future climate change.

약물검사에서 관리시료의 농축을 이용한 보고 가능 범위의 설정에 대한 연구 (A Study of Reportable Range Setting through Concentrated Control Sample)

  • 장상우;김남용;최호성;박용원;윤근영
    • 대한임상검사과학회지
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    • 제36권1호
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    • pp.13-18
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    • 2004
  • This study was designed to establish working range for reoportable range in own laboratory in order to cover the upper and lower limits of the range in test method. We experimented ten times during 10 days for setting of reportable range with between run for method evaluation. It is generally assumed that the analytical method produces a linear response and that the test results between those upper and lower limits are then reportable. CLIA recommends that laboratories verify the reportable range of all moderate and high complexity tests. The Clinical Laboratory Improvement Amendments(CLIA) and Laboratory Accreditation Program of the Korean Society for Laboratory Medicine states reportable range is only required for "modified" moderately complex tests. Linearity requirements have been eliminated from the CLIA regulations and from others accreditation agencies, many inspectors continue to feel that linearity studies are a part of good lab practice and should be encouraged. It is important to assess the useful reportable range of a laboratory method, i.e., the lowest and highest test results that are reliable and can be reported. Manufacturers make claims for the reportable range of their methods by stating the upper and lower limits of the range. Instrument manufacturers state an operating range and a reportable range. The commercial linearity material can be used to verify this range, if it adequately covers the stated linear interval. CLIA requirements for quality control, must demonstrate that, prior to reporting patient test results, it can obtain the performance specifications for accuracy, precision, and reportable range of patient test results, comparable to those established by the manufacturer. If applicable, the laboratory must also verify the reportable range of patient test results. The reportable range of patient test results is the range of test result values over which the laboratory can establish or verify the accuracy of the instrument, kit or test system measurement response. We need to define the usable reportable range of the method so that the experiments can be properly planned and valid data can be collected. The reportable range is usually defined as the range where the analytical response of the method is linear with respect to the concentration of the analyte being measured. In conclusion, experimental results on reportable range using concentrated control sample and zero calibrators covering from highest to lowest range were salicylate $8.8{\mu}g/dL$, phenytoin $0.67{\mu}g/dL$, phenobarbital $1.53{\mu}g/dL$, primidone $0.16{\mu}g/dL$, theophylline $0.2{\mu}g/dL$, vancomycine $1.3{\mu}g/dL$, valproic acid $3.2{\mu}g/dL$, digitoxin 0.17ng/dL, carbamazepine $0.36{\mu}g/dL$ and acetaminophen $0.7{\mu}g/dL$ at minimum level and salicylate $969.9{\mu}g/dL$, phenytoin $38.1{\mu}g/dL$, phenobarbital $60.4{\mu}g/dL$, primidone $24.57{\mu}g/dL$, theophylline $39.2{\mu}g/dL$, vancomycine $83.65{\mu}g/dL$, valproic acid $147.96{\mu}g/dL$, digitoxin 5.04ng/dL, carbamazepine $19.76{\mu}g/dL$, acetaminophen $300.92{\mu}g/dL$ at maximum level.

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임상보고 가능범위의 실증적 연구 (An Empirical Study of the Clinically Reportable Range in Clinical Chemistry)

  • 장상우;이상곤;최호성;송은영;박용원;이인애
    • 대한임상검사과학회지
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    • 제39권1호
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    • pp.31-36
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    • 2007
  • The purpose of the clinically reportable range (CRR) in clinical chemistry is to estimate linearity in working range. The reportable range includes all results that may be reliably reported, and embraces two types of ranges: the analytical measurement range (AMR) is the range of analyte values that a method can directly measure on the specimen without any dilution, concentration, or other pretreatment not part of the usual assay process. CAP and JCAHO require linearity on analyzers every six months. The clinically reportable range is the range of analyte values that a method can measure, allowing for specimen dilution, concentration, or other pretreatment used to extend the direct analytical measurement range. The AMR cannot exceed the manufacturer's limits. Establishing AMR is easily accomplished with Calibration Verification Assessment and experimental Linearity. For example: The manufacturer states that the limits of the AST on their instrument are 0-1100. The lowest level that could be verified is 2. The upper level is 1241. The verified AMR of the instrument is 2-1241. The lower limit of the range is 2, because that is the lowest level that could be verified by the laboratory. The laboratory could not use the manufacturer's lower limit of 2 because they have not proven that the instrument values below 2 are valid. The upper limit of the range is 1241, because although the lab has shown that the instrument is linear to 1241, the manufacturer does not make that claim. The laboratory needs to demonstrate the accuracy and precision of the analyzer, as well the validation of the patient AMR. Linearity requirements have been eliminated from the CLIA regulations and from the CAP inspection criteria, however, many inspectors continue to feel that linearity studies are a part of good lab practice and should be encouraged. If a lab chooses to continue linearity studies, these studies must fully comply with the calibration/calibration verification requirements of CLIA and/or CAP. The results of lower limit and upper limit of clinically reportable range were total protein (2.1 - 79.9), albumin (1.3 - 39), total bilirubin (0.2 - 106.2), alkaline phosphatase (13 - 6928.2), aspartate aminotransferase (24 - 7446), alanine aminotransferase (13 - 6724.2), gamma glutamyl transpeptidase (16.64 - 9904.2), creatine kinase (15.26 - 4723.8), lactate dehydrogenase (127.66 - 13231.8), creatinine (0.4 - 129.6), blood urea nitrogen (8.67 - 925.8), uric acid (1.6 - 151.2), total cholesterol (48.52 - 3162), triglycerides (36.91 - 3367.8), glucose (31 - 4218), amylase (21 - 6694.2), calcium (3.1 - 118.2), inorganic phosphorus (1.11 - 108), HDL (11.74 - 666), NA (58.3 - 1800), K (1.0 - 69.6), CL (38 - 1230).

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등가가스를 이용한 부분예혼합 가스기기의 호환성 판정법 (Estimation Method of the Interchangeability Using Equivalent Gases in a Partial Premixed Gas Appliance)

  • 김종민;이승로;하영철;이성민;이창언
    • 대한기계학회논문집B
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    • 제34권8호
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    • pp.761-766
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    • 2010
  • 본 연구는 등가가스를 이용하여 다양한 조성의 천연가스에 대한 부분예혼합 가스기기의 호환성 판정법을 실험을 통하여 검토 제시하였다. 본 판정법을 위해, 가정용 가스레인지를 이용 등가가스와 천연가스의 화염을 비교 하였으며, 화염의 부상 및 불완전연소에 대해 측정을 하여 KS 규격과 비교하였다. 그 결과, 등가가스와 천연가스의 화염은 화염길이, 화염색, 화염모양 등의 차이가 거의 없었다. 또한 화염의 부상 발생은 웨버지수 51 MJ/$m^3$ 이상에서 안정함을 보였으며, 불완전 연소지수의 경우, 웨버지수 56.3 MJ/$m^3$에서 CO 농도가 95~100 ppm 정도를 보여주었다. 결과적으로 천연가스에 대한 화염의 부상과 불완전연소에 대해 호환 범위를 웨버지수 51~56.3 MJ/$m^3$로 제안하였으며, 이 범위 내의 천연가스는 국내 가정용 부분예혼합 가스기기에 대해 호환 가능하다는 의미이다.

$\beta$ - 분포를 갖는 센서의 방향각 오차로 인한 거리 오차의 통계적 분석 (Statistical Analysis of Ranging Errors by using $\beta$-Density Angular Errors due to Heading Uncertainty)

  • 김종성
    • 한국음향학회:학술대회논문집
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    • 한국음향학회 1984년도 추계학술발표회 논문집
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    • pp.100-106
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    • 1984
  • Traditional methods for estimating the location of underwater target, i.e. the triangulation method and the wavefront curvature method, have been utilized. The location of a target is defined by the range and the bearing, which estimates can be obtained by evaluating the time delay between neighboring sensors. Many components of error occur in estimating the target range, among which the error due to the fluctuation of heading angle is outstanding. In this paper, the wavefront curvature method was used. We considered the error due to the heading fluctuation as the $\beta$-density process, from which we analized the range estimates with $\beta$-density function exist in some finite limits, and its mean value and variation are depicted as a function of true range and heading fluctuation. Given heading angles and sensor separation, maximum estimated heading errors are presented as a function of true range.

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지산통(芝山統)의 토양특성(土壤特性) 범위(範圍) 검정(檢定) (Test of Official Range in Characteristics for Jisan Soil Series)

  • 정석재;박창서;현근수;문준;엄기태
    • 한국토양비료학회지
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    • 제22권2호
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    • pp.81-85
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    • 1989
  • 우리나라의 답토양중(畓土壤中) 분포면적(分布面積)이 가장 넓은(전국(全國) 113개(個) 지역(地域)에서 작도(作圖)되었음) 지산통(芝山統)의 지역별(地域別) 대표단면(代表斷面)을 가지고 토양(土壤) 설정시(設定時) 정의(定義)된 사양특성(士壤特性)의 허용설정(許容設定) 범위(範圍)와 정확도(正確度)를 분석(分析)하였다. 1. 표토(表土)의 특성(特性) 평균치(平均値)는 층위(層位)두께에서 23.2cm, 토성(土性) 양토(壤土) pH 5.7 그리고 염기포화도(鹽基飽和度) 64%로 모두 설정범위내(設定範圍內)에 속(屬)하였다. 2. 심토(心土)의 특성(特性)도 평균치(平均値)는 층위(層位)두께에서 64.0cm, 점토함량(粘土含量) 23.8%, 토성(土性) 양토(壤土), pH6.2 그리고 염기포화도(鹽基飽和度) 73 %로 있었고 기층(基層)의 경우에도 특성(特性) 평균치(平均値)는 모두 설정범위내(說定範圍內)에 있었다. 3. 유효토심(有效土深)과 평균치(平均値)는 87.2cm 그리고 층위조성(層位組成)은 A-B-C 층위(層位)로 허용설정(許容設定) 범위내(範圍內)에 존재(存在)하였다. 4. 심토(心土)의 정확도(正確度)는 0.687~0.929 범위내(範圍內)에 있었으며, 유효토심(有效土深)과 층위조성(層位造成)의 정확도(正確度)는 각각(各各) 0.723 및 0.920이었다.

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Recorder with automatic scaling function

  • Tomita, Takehiko;Tohara, Masahiro
    • 제어로봇시스템학회:학술대회논문집
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    • 제어로봇시스템학회 1988년도 한국자동제어학술회의논문집(국제학술편); 한국전력공사연수원, 서울; 21-22 Oct. 1988
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    • pp.891-895
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    • 1988
  • We discuss what kind of scale is suitable for analog signal recording paper from the viewpoint of human engineering. We show a method for automatically generating a suitable scale from the higher and lower limits of the recording range.

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