• 제목/요약/키워드: motor oil

검색결과 242건 처리시간 0.018초

연료전지자동차용 수소제조와 저장·운반기술동향 (Technical Trends of Hydrogen Manufacture, Storage and Transportation System for Fuel Cell Vehicle)

  • 길상철;황용길
    • 자원리싸이클링
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    • 제25권1호
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    • pp.48-59
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    • 2016
  • 화석연료를 사용하는 선박이나 자동차는 $CO_2$가스를 과대하게 발생하므로 지구 온난화에 영향을 주기 때문에 화석연료 대신 수소를 사용하는 수소연료전지자동차(FCV)가 크게 각광을 받고 있다. 우리나라는 현대자동차가 FCV자동차를 미국, 일본, 독일 등의 선진국들의 자동차회사와 경쟁적으로 개발하고 있다. 수소는 제철소의 코크스 공장, 서유화학공장의 부산물로 얻으며, 석탄, 메탄가스 등을 고온에서 증기와 반응시켜서 메탄 수증기개질법과 압력스윙흡착법 또는 막분리형멤브레인개질 법을 이용한 수소분리형개질방법으로 고순도 수소를 제조하거나 물을 전기분해하여 제조한다. 수소는 전자공업, 금속 및 화학공업, 로켓 연료 및 공장, 병원, 가정용 등의 연료전지시스템이나 FCV의 연료로 사용하고 있다. 수소의 저장은 수소용기에 수소를 압축하는 방법과 액화수소로 저장하는 방법이 일반적이고, 최근 수소화물이나 유기화학하이드라이드법으로 저장하여 수소스테이션에 운반해서 사용한다. 우리나라는 현재 13개소의 수소스테이션이 가동 중에 있으며, 향후 43개소를 설치할 계획이다.

MPTP로 유도된 Parkinson's disease 동물 모델에서 열다한소탕 가감방 (MYH)의 신경 세포 보호 효과 (Neuroprotective Effects of Modified Yuldahanso-tang (MYH) in a Parkinson's Disease Mouse Model)

  • 고가연;김윤하;안택원
    • 사상체질의학회지
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    • 제27권2호
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    • pp.270-287
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    • 2015
  • Objectives To evaluate the neuroprotective effects of modified Yuldahanso-tang (MYH) in a Parkinson's disease mouse model. Methods 1) Four groups (each of 8 rats per group) were used in this study. 2) The neuroprotective effect of MYH was examined in a Parkinson's disease mouse model. C57BL/6 mice treated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP, 30 mg/kg/day), intraperitoneal (i.p.) for 5 days. 3) The brains of 2 mice per group were removed and frozen at $-20^{\circ}C$, and the striatum-substantia nigra part was seperated. The protein volume was measured by Bradford method following Bio-Rad protein analyzing kit. Using mouse/Rat Dopamine ELISA Assay Kit. 4) The brains of 2 mice per group were separated and removed. TH-immunohistochemical was examined in the MPTP-induced Parkinson's disease mice to evaluate the neuroprotective effects of MYH on ST and SNpc. 5) Two mice out of each group were anesthetized and skulls were opened from occipital to frontal direction to take out the brains. The brains added TTC solution for 20 minutes for staining. 6) The water tank used for morris water maze test was filled with $28^{\circ}C$ water, and a round platform of 10cm in diameter was installed for mice to step on. The study was carried out once a day within 30 seconds, keep exercising to step on the platform in the pool. 7) The brains of two mice out of each group were fixed in 10% formaldehyde solution and paraphillin substance was infiltrated. They were fragmented by microtome, and observed under an optical microscope after Hematoxylin & Eosin staining. 8) A round acrylic cylinder with its upper side open was filled with clean water and depressive mouse models were forced to swim for 15 minutes. After 24 hours the animals were put in the same equipment for 5 minutes and were forced to swim. 9) The convenient, simple, and accurate high-performance liquid chromatography (HPLC) method was established for simultaneous determination of Neurotransmitters in MPTP-MYH group. Results 1) MYH possess Dopamine cell protective effect on MPTP-induced injury in striatum and substantia nigra pars compacta. 2) MYH inhibits the loss of tyrosine hydroxylase-immunoreacitive (TH-IR) cells in the striatum and substantia nigra pars compacta on MPTP-induced injury in C57BL/6 mice. 3) MYH possesses improvement effect on MPTP-induced memory deterioration in C57BL/6 mice through the reduction of prolongated Sort of lost time by MPTP injection using the Morris water maze test. 4) MYH possesses hippocampal neuron protective effect on MPTP-induced injury in C57BL/6 mice. 5) MYH possesses improvement effect on MPTP-induced motor behaviour deficits and depression in C57BL/6 mice through the reduction of prolongated losing motion by MPTP injection using the Forced swimming test. 6) MYH increases serotonin product amount on MPTP-induced injury in C57BL/6 mice. Conclusions This experiment suggests that the neuroprotective effect of MYH is mediated by the increase in Dopamin, TH-ir cell, Hippocampus and Serotonin. Furthermore, MYH essential oil may serve as a potential preventive or therapeutic agent regarding Parkinson's disease.