• 제어로봇시스템학회:학술대회논문집
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• 2001.10a
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• pp.111.2-111
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• 2001

The research focuses on controlling a gap to measure the surface defect in semi-conductor fabrication device. The measurement is available accompanying a near field image gap control. In this article, a pneumatic servo system is adopted for the near field gap control. The advantage of the pneumatic servo system is on the preventing the possibility of contacting the device to the wapper surface, fence arising fatal damage. Furthermore, the air from the pneumatic system blows the some particle on the wapper during controlling. The target gap is less than 20 $\mu$m and the gap should keep same amount while the device moves around the surface. The experiment by the pneumatic servo control system is done by employing a simple PID control, and the tracking performance is remarkably verified. The target gap is set from 10 $\mu$m to 100 $\mu$m ...

• Proceedings of the Korean Society of Computer Information Conference
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• 2016.01a
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• pp.87-90
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• 2016

현재 한국 군부대에서 사용되고 있는 표적구동장치는 1990년도에 만들어진 재래식 장비로서 노후화 및 부품교체 난제로 인하여 지속적인 시스템의 오류와 이에 따른 장비 가동률 저하 등의 문제로 실전적인 사격 훈련이 어렵다. 이에 본 연구에서는 보다 효과적인 훈련을 진행하고자 복합 구동 표적장치를 개발하였다. 본 연구에서 개발된 복합 구동 표적장치는 Up-down, Swing, Turn, Rotary 방식의 표적 구동을 원격으로 제어하여 다양한 사격 및 전술 훈련 적용 가능하도록 제작되었으며, 또한 사격진행 통제 결과를 통제관 혼자서 총괄 운용이 가능한 모니터링 시스템을 구축하였다. 그리고 현재 각 부대에 설치되어 있는 표적구동장치 및 전술훈련 컨트롤러는 유선을 통한 시리얼통신 및 중앙 분배식 전원공급시스템으로서 운영설비를 위하여 과도한 배관배선 등의 공사가 별도로 시행되어야 하는 문제점이 있다. 따라서 본 연구에서는 이러한 문제점을 해결할 수 있도록 무선 통신시스템방식을 적용하여 다양한 훈련지역에 호환 적용될 수 있는 장비를 개발함으로써 훈련장 시설건립을 위한 부담을 줄이고, 운영의 극대화를 확보할 수 있도록 경제적, 기술적 효과를 추구하였다.

• Proceedings of the Korean Vacuum Society Conference
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• 2013.08a
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• pp.273-273
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• 2013

Recently, Point-of-care (POC) testing microdevices enable to do the patient monitoring, drug screening, pathogen detection in the outside of hospital. Immunochromatographic strip (ICS) is one of the diagnostic technologies which are widely applied to POC detection. Relatively low cost, simplicity to use, easy interpretations of the diagnostic results and high stability under any circumstances are representative advantages of POC diagnosis. It would provide colorimetric results more conveniently, if the genetic analysis microsystem incorporates the ICS as a detector part. In this work, we develop a reverse transcriptase-polymerase chain reaction (RT-PCR) microfluidic device integrated with a ROSGENE strip for colorimetric influenza H1N1 virus detection. The integrated RT-PCR- ROSGENE device is consist of four functional units which are a pneumatic micropump for sample loading, 2 ${\mu}L$ volume RT-PCR chamber for target gene amplification, a resistance temperature detector (RTD) electrode for temperature control, and a ROSGENE strip for target gene detection. The device was fabricated by combining four layers: First wafer is for RTD microfabrication, the second wafer is for PCR chamber at the bottom and micropump channel on the top, the third is the monolithic PDMS, and the fourth is the manifold for micropump operation. The RT-PCR was performed with subtype specific forward and reverse primers which were labeled with Texas-red, serving as a fluorescent hapten. A biotin-dUTP was used to insert biotin moieties in the PCR amplicons, during the RT-PCR. The RT-PCR amplicons were loaded in the sample application area, and they were conjugated with Au NP-labeled hapten-antibody. The test band embedded with streptavidins captures the biotin labeled amplicons and we can see violet colorimetric signals if the target gene was amplified with the control line. The off-chip RT-PCR amplicons of the influenza H1N1 virus were analyzed with a ROSGENE strip in comparison with an agarose gel electrophoresis. The intensities of test line was proportional to the template quantity and the detection sensitivity of the strip was better than that of the agarose gel. The test band of the ROSGENE strip could be observed with only 10 copies of a RNA template by the naked eyes. For the on-chip RT-PCR-ROSGENE experiments, a RT-PCR cocktail was injected into the chamber from the inlet reservoir to the waste outlet by the micro-pump actuation. After filling without bubbles inside the chamber, a RT-PCR thermal cycling was executed for 2 hours with all the microvalves closed to isolate the PCR chamber. After thermal cycling, the RT-PCR product was delivered to the attached ROSGENE strip through the outlet reservoir. After dropping 40 ${\mu}L$ of an eluant buffer at the end of the strip, the violet test line was detected as a H1N1 virus indicator, while the negative experiment only revealed a control line and while the positive experiment a control and a test line was appeared.