국제해사기구는 국제해운의 온실가스 배출을 줄이기 위한 전략을 채택하였으며, 선박 기인 온실가스 배출을 줄이기 위해 보다 강화된 목표를 설정하고 있다. 액체수소를 기화시켜 연료로 사용하는 고분자 전해질 연료전지는 이러한 규제를 준수하기 위한 유망한 기 술 중 하나로 평가받고 있다. 일반적으로 선박시스템 설계는 선급의 규정에 따라야 하지만 환경규제가 강화됨에 따라 새로운 연료와 시 스템의 도입이 가속화되고 있으며, 이로 인해 규정개발이 기술의 도입을 따라가지 못하는 경우도 발생하고 있다. 이러한 격차를 해소하기 위해, 본 연구에서는 수소 연료가스공급 시스템을 대상으로 위험요소 및 운전분석 기법(HAZOP)과 보호계층분석 기법(LOPA)을 결합하여 신기술의 안전성을 검증하는 방법을 제시하였다. 먼저 HAZOP을 통해 위험 시나리오를 식별하고, LOPA를 통해 정성적인 HAZOP 결과를 정량적으로 보완하였다. 초기사건의 빈도와 독립보호계층(IPL)들의 작동 요구시 고장 확률(PFD)을 계산하였다. 기존 IPL의 적절성을 결정 하기 위해, 예상되는 완화 정도를 가정한 허용기준과 비교하였으며, 필요한 경우, 추가 IPL을 권장하였다. 본 연구를 통해서 HAZOP-LOPA 기법이 조선해양 분야에서 신기술의 안전성을 평가할 수 있는 잠재력을 가지고 있음을 확인하였다.

Background : Codonopsis lanceolata is a flowering perennial climber. The roots are used as medicinal materials or vegetables. C. lanceolata is distributed in India and East Asia such as China, Japan as well as Korea. Recently, demand for C. lanceolata is increasing as a healthy food. In South Korea, this plant is widely cultivated in Gangwon-do province. Although, C. lanceolata is one of the most important medicinal plants in Korea, it is easy to be confused with other species of the same genus. Simple sequence repeat (SSR) marker is a powerful tool for distinguish specific species. In addition, there are many studies that show species-specific polymorphisms in chloroplasts SSR. In this study, we developed chloroplast SSR markers that can distinguish C. lanceolata from 6 Codonopsis species. Methods and Results : We collected 6 Codonopsis species include C. lanceolata. and extrated DNA using CTAB method. The DNA was diluted to 10 ng/㎕ and kept at –20℃. We designed the primer sets using CLC Main Workbench based on chloroplast DNA SSR region of C. lanceolata. PCR was performed using three independent plants for each species. Conclusion : We designed six primer sets from six SSR regions of C. lanceolata cpDNA. All of the primer sets amplified the amplicon effectively. Two of the 6 primer sets had polymorphism. We could distinguish C. lanceolata from 6 Codonopsis species using two primer sets.

Background : Angelica gigas is a monocarpic biennial or short lived perennial plant. A. gigas, also called Dang Gui or Korean Angelica, is a major medicinal herb used in Asian countries such as Korea, Japan and China. In Korea, we are using the roots of A. gigas, but, they are using Angelica sinensis in China and Angelica acutiloba in Japan to obtain many active constituents. The biggest problem in the using of A. gigas would be the confusion with A. acutiloba or A. sinensis. These three plants can't be distinguished by appearance. And the constituent ratios of the three plants are different. This confusion can cause an accident or the pharmaceutical effects do not meet the expectations. In this study, we developed chloroplast SSR markers that can distinguish A. gigas, A. acutiloba and A. sinensis. Methods and Results : We collected A. gigas, A. acutiloba and A. sinensis. and extrated DNA using CTAB method. The DNA was diluted to 10 ng/㎕ and kept -20℃. We designed the primer sets using CLC Main Workbench based on chloroplast DNA SSR region of A. gigas. PCR were performed on the three angelica plant samples (in 5 repeat). Conclusion : We made five primer sets from five SSR regions of A. gigas cpDNA. All of the primer sets amplified the amplicon effectively. Two of the 5 primer sets had polymorphism. We can distinguish A. gigas, A. acutiloba, and A. sinensis using the 2 primer sets