• KIEAE Journal
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• v.4 no.3
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• pp.87-94
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• 2004

The purpose of this study is to improve thermal environment of telecommunication equipment rooms that hold TDX-10, TDX-100, 5ESS-2000, PCM of the latest telecommunication equipment. Analysis program is used the commercial CFD code, Star-CD and DOE-2.1E. The result has been compared by the energy consumption and the temperature contour at the 1 m height of room for each case. Different methods such as the relocation of the existing air-conditioner, the inflow of the ambient air into room, the installation of the forced fan and the cooling system equipment of the duct-connection type have been used to test for improvement of thermal environment. The analysis shows that most efficient method is the inflow of the ambient air into room but auxiliary equipment should be needed to prevent the local thermal spot.

• ETRI Journal
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• v.8 no.2
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• pp.100-108
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• 1986

본고에서는 TDX-1의 유지보수 기능으로서 개발된 각 기능별 개요 및 특성에 대하여 기술함으로써 TDX-1의 기능을 이해하거나 타 교환기와의 특성을 비교하는데 도움을 줄수 있도록 하였다. TDX-1의 유지보수 기능은 그 수행대상에 따라 프로세서계와 텔리포니계 유지보수 기능으로 구분된다. 프로세서계의 유지보수 기능에는 시스팀 시동, 프로세서 상태처리, 프로세서 시험, 시스팀 클럭관리와 프로세서 장애처리 기능 등이 있으며 텔리포니계 유지보수 기능에는 시스팀 장애 처리, 네트워크 상태 처리, 네트워크 시험과 시스팀 경보처리 기능 등이 속한다.

• Information and Communications Magazine
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• v.15 no.6
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• pp.51-62
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• 1998

• Proceedings of the Korean Institute of Information and Commucation Sciences Conference
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• 2003.05a
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• pp.226-230
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• 2003

In this thesis I analyzed that V5.2 protocol function is effective to fulfill all of the services that are provided at the existing local exchange. I analyzed this in five methods that refer to ETSI inside patronage. I experimented turnaround time by Start-up method and verified V5.2 protocol function when Start-up. Also I confirmed stability of system by the reconstruction-ability experiment related E1 switch over. I verified V5.2 protocol function through PSTN call process that uses a special service test and local call simulator. As a result of experiment, I confirmed the best method when simultaneous Start-up. V5.2 protocol function was excellent and It becomes switch over at 1/1000 seconds when E1 is out of service. V5.2 protocol function was effective to fulfill all of the special services that are provided at local exchange and its long call process ability was superior to KT standard with 4 fails in 20000 calls. Through the experiment, it was proved that V5.2 interface will become a significant element of communication network when after LE side expanse of v5 interface ID with TDX-100 exchanger and the AN occurrences OOS by message transmission limit and call disconnect when E1 switch over are improved.

• Proceedings of the Korean Society of Precision Engineering Conference
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• 2002.05a
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• pp.432-437
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• 2002

DSPA311(Analog Subscriber Line Board Assembly) is offer the interface of between analog subscriber and TDX-100 exchange system. DSPA311 is belong ASI block, accommodate dial and MFC telephone subscriber of 32 channel, and voice signal designed for interface with TSW, and 2 and 4 wire loop impedance is 600 (ohm). DSPA311 is consist 4 channel daughter beard QSLM-10(Quad Subscriber Line Module-10) and perform BORSCHT and be possible A/U-law select and GAIN value control by data control of DSPA171(Device controller I). In this Paper, We described the function test program for the DSPA311 Board by using the HP3070CT combinational test system, and an unmanned automatic test system.

• YAKHAK HOEJI
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• v.47 no.5
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• pp.266-270
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• 2003

We evaluated four commercially available methamphetamine immunoassays for their relative cross-reactivities of amphetamine analogues in human urine: Abbott TDx, Vitalab Selectra and on-site test kits (Accusign MET, SD bioline MET). High cross-reactivities were shown at designer's drugs such as methylenedioxyamphetamine (MDA), methylenedioxymethamphetamine (MDMA) and methylenedioxyethylamphetamine (MDEA) in all of the tested immunoassays. Methoxyphenamine, fenfluramine and phentermine were positive in TDx and Selectra, but were not positive in on-site test kits. Pseudoephedrine, norpseudoephedrine, ephedrine, norephedrine, MDMA, MDA, fenfluramine and phentermine were detected by gas chromatography/mass spectrometry(GC/MS) in false positive urines. Since the overall specificity of any of the devices was not 100％, we found it is important to confirm any positive screening test result, so we developed simultaneous determination of amphetamine analogues in urines. After alkalinization of the urine samples with 6-N NaOH, the analytes were extracted using ethyl acetate, derivatized with pentafluoropropyl anhydride (PFPA) prior at GC/MS analysis.

• YAKHAK HOEJI
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• v.52 no.6
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• pp.419-425
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• 2008

A qualitative and quantitative analytical method was developed for detection of methamphetamine (MA) and its main metabolite amphetamine (AM) in oral fluid. Oral fluids of eleven drug abusers were provided by Police, specimens were collected by stimulation with a cotton swab treated with 20 mg of citric acid ($Salivette^{(R)}$; Sarstedt, USA). As the preliminary test, oral fluid samples were screened for amphetamines by Fluorescence Polarization Immunoassay (TDxFLx, Abbott Co.). Extraction for MA was performed using solid-phase extraction (SPE) by $RapidTrace^{TM}$ (Zymark, USA) with mixed mode cation exchange cartridge, CLEAN $SCREEN^{(R)}$ (130 mg/3 ml, UCT) after dilution with phosphate buffer. Samples were evaporated and derivatized by pentafluoropropionic acid anhydride (PFPA). Quantitation of MA and AM was performed by gas chromatography-mass spectrometry (GC-MS) using selective ion monitoring (SIM), the quantitation ions were m/z 204 (MA), 208 (MA-$D_5$), 190 (AM) and 194 (AM-$D_5$). The selectivity, linearity of calibration, limit of detection (LOD) and quantification (LOQ) within- and between day precision, accuracy and recoveries were examined as parts of the method validation. All oral fluid samples gave positive results to immunoassay for MA (cut-off level, 50 ng/ml as d-amphetamine). Concentrations of MA and AM by GC-MS in eleven samples were ranged 104.2${\sim}$4603.3 ng/ml and 32.4${\sim}$268.6 ng/ml, respectively. Extracted calibration curves of MA and AM were linear over the two concentration range of 1${\sim}$100 and 50${\sim}$1000 ng/ml with correlation coefficient of above 0.999. LOQ of MA and AM was 1 and 3 ng/ml, respectively. The intraand inter-day run precisions (CV) for MA and AM were less than 10%, and the accuracies (bias) for MA and AM were also less than 10% at the two different concentrations 5 and 100 ng/ml at low calibration range, 50 and 1000 ng/ml at high calibration range. The absolute recoveries of MA and AM at low and high calibration ranges were more than 82% and 75%, respectively. In this study the qualitative and quantitative analytical method of MA in oral fluid was established. Oral fluid testing may detect drug use in past hours because of its shorter detection window than urine, and be useful in post-accident situations. So oral fluids will be most useful for testing drug abuse in the driving under the influence of drug (DUID) as the alternative specimens of urine.