• 접착 및 계면
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• 제4권1호
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• pp.9-17
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• 2003

오늘날 산업에서는 환경오염의 줄이고 에너지 절약에 기여할 수 있다는 이유에서 용매를 사용하지 않는 UV 하드코팅재료의 개발이 점차로 많은 주의를 끌고 있다. 본 연구는 실질적으로 산업에 이용될 수 있는 실리콘아크릴레이트(SAOC)를 포함하고 있는 UV 경화코팅제를 개발하고자 수행되었다. 실험의 결과, 수지조성물 중 SAOC의 형태나 농도가 UV 경화필름의 여러 가지 물성에 영향을 주었다. SAOC가 수지조성물에 도입되었을 때 경화된 필름의 물성은 SAOC가 함유되지 않은 도막과 비교하여 개선되었다. 특히, UV 하드 코팅의 내화학성, 내마모성, 내후성과 같은 성질들은 향상되었으며, 코팅된 폴리카보네이트 기재의 충격특성은 코팅되지 않은 PC에 비해 개선되었다. 30 wt% SAOC를 함유하고 있는 경화필름이 가장 좋은 물성을 나타내었다.

• 폴리머
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• 제30권2호
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• pp.140-145
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• 2006

디스플레이용 기판으로 사용하고 있는 유리기판은 무겁고 깨지기 쉬우므로 이를 폴리설폰, 폴리에테르설폰, 폴리카보네이트, 폴리에틸렌테레프탈레이트 환상형 올레핀 고분자 등의 플라스틱으로 대체하는 연구가 많이 이루어지고 있다. 플라스틱 기판은 가볍고, 내충격성이 뛰어나며, 유연하고 연속가공이 가능한 장점을 가지고 있다. 그러나 여러 유기용매에 녹는 특성을 가지고 있다. 디스플레이 제조 공정에서는 여러 유기용매에 노출되므로 이에 대한 내화학성이 필요하다. 그러므로 본 연구에서는 폴리설폰에 곁가지로 이미드 가교기를 도입하여 내화학성을 향상시키는 연구를 하였다. 곁사슬기에 의해 가교된 폴리설폰 필름은 용해도 조사 결과 내화학성이 향상되었음을 확인할 수 있었다. 내화학성 측정 결과 MeOH, THF, DMSO, NMP 등의 유기용매에 불용성을 보였다. 또한 15% 이상 낮은 열팽창계수를 보여 열에 대한 치수안정성이 개선되었으며 유리 전이 온도도 이미드기의 도입에 따라 $180^{\circ}C$ 에서 $252^{\circ}C$ 로 증가하였다. 이와 같이 제조한 이미드 곁가지로 가교된 폴리설폰은 광학적 특성이 우수하면서도 내화학성이 뛰어나 유연성 플라스틱 기판으로 사용이 가능하다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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• pp.88-89
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• 2013

A variety of influenza A viruses from animal hosts are continuously prevalent throughout the world which cause human epidemics resulting millions of human infections and enormous industrial and economic damages. Thus, early diagnosis of such pathogen is of paramount importance for biomedical examination and public healthcare screening. To approach this issue, here we propose a fully integrated Rotary genetic analysis system, called Rotary Genetic Analyzer, for on-site detection of influenza A viruses with high speed. The Rotary Genetic Analyzer is made up of four parts including a disposable microchip, a servo motor for precise and high rate spinning of the chip, thermal blocks for temperature control, and a miniaturized optical fluorescence detector as shown Fig. 1. A thermal block made from duralumin is integrated with a film heater at the bottom and a resistance temperature detector (RTD) in the middle. For the efficient performance of RT-PCR, three thermal blocks are placed on the Rotary stage and the temperature of each block is corresponded to the thermal cycling, namely $95^{\circ}C$ (denature), $58^{\circ}C$ (annealing), and $72^{\circ}C$ (extension). Rotary RT-PCR was performed to amplify the target gene which was monitored by an optical fluorescent detector above the extension block. A disposable microdevice (10 cm diameter) consists of a solid-phase extraction based sample pretreatment unit, bead chamber, and 4 ${\mu}L$ of the PCR chamber as shown Fig. 2. The microchip is fabricated using a patterned polycarbonate (PC) sheet with 1 mm thickness and a PC film with 130 ${\mu}m$ thickness, which layers are thermally bonded at $138^{\circ}C$ using acetone vapour. Silicatreated microglass beads with 150~212 ${\mu}L$ diameter are introduced into the sample pretreatment chambers and held in place by weir structure for construction of solid-phase extraction system. Fig. 3 shows strobed images of sequential loading of three samples. Three samples were loaded into the reservoir simultaneously (Fig. 3A), then the influenza A H3N2 viral RNA sample was loaded at 5000 RPM for 10 sec (Fig. 3B). Washing buffer was followed at 5000 RPM for 5 min (Fig. 3C), and angular frequency was decreased to 100 RPM for siphon priming of PCR cocktail to the channel as shown in Figure 3D. Finally the PCR cocktail was loaded to the bead chamber at 2000 RPM for 10 sec, and then RPM was increased up to 5000 RPM for 1 min to obtain the as much as PCR cocktail containing the RNA template (Fig. 3E). In this system, the wastes from RNA samples and washing buffer were transported to the waste chamber, which is fully filled to the chamber with precise optimization. Then, the PCR cocktail was able to transport to the PCR chamber. Fig. 3F shows the final image of the sample pretreatment. PCR cocktail containing RNA template is successfully isolated from waste. To detect the influenza A H3N2 virus, the purified RNA with PCR cocktail in the PCR chamber was amplified by using performed the RNA capture on the proposed microdevice. The fluorescence images were described in Figure 4A at the 0, 40 cycles. The fluorescence signal (40 cycle) was drastically increased confirming the influenza A H3N2 virus. The real-time profiles were successfully obtained using the optical fluorescence detector as shown in Figure 4B. The Rotary PCR and off-chip PCR were compared with same amount of influenza A H3N2 virus. The Ct value of Rotary PCR was smaller than the off-chip PCR without contamination. The whole process of the sample pretreatment and RT-PCR could be accomplished in 30 min on the fully integrated Rotary Genetic Analyzer system. We have demonstrated a fully integrated and portable Rotary Genetic Analyzer for detection of the gene expression of influenza A virus, which has 'Sample-in-answer-out' capability including sample pretreatment, rotary amplification, and optical detection. Target gene amplification was real-time monitored using the integrated Rotary Genetic Analyzer system.