Photolysis of bromoethylene at 163.3nm163.3nm에서 브로모에틸렌의 광분해 반응에 관한 연구

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dc.contributor.advisorLee, Yoon-Sup-
dc.contributor.advisor이윤섭-
dc.contributor.authorJoh, Hyeon-Soo-
dc.contributor.author조현수-
dc.date.accessioned2011-12-13T04:58:08Z-
dc.date.available2011-12-13T04:58:08Z-
dc.date.issued1989-
dc.identifier.urihttp://library.kaist.ac.kr/search/detail/view.do?bibCtrlNo=66577&flag=dissertation-
dc.identifier.urihttp://hdl.handle.net/10203/32549-
dc.description학위논문(석사) - 한국과학기술원 : 화학과, 1989.2, [ iv, 41 p. ]-
dc.description.abstractA vacuum ultraviolet photolysis of bromoethylene was studied in the pressure range of 1-70 Torr at 163.3nm using bromine atom resonance lamp. The result demonstrates the two decomposition mode, i.e., one for molecular elimination of HBr to form acetylene, and the other for C-Br bond cleavage to form vinyl radical. The principal products were found to be $C_2H_2,\;C_2H_4,\;C_2H_4Br_2$, and small amount of $C_4H_7Br$. The HBr was added as radical capture to obtain information about the primary process. The pressure effect by adding inert gases, i.e., $CF_4$ and He, was also observed in the presence and absence of HBr. The ratio of quantum yield, $\Phi(C_2H_2)/\Phi(C_2H_2)$, was decreased as the pressure increased in absence of HBr. But with the presence of HBr the ratio remains constant as the pressure increased. This observation may be attributed by the fact that "hot" vinyl radical, produced from C-Br bond cleavage, decomposes to acetylene and hydrogen atom. This process has been quenched by adition of HBr, radical capture.eng
dc.languageeng-
dc.publisher한국과학기술원-
dc.titlePhotolysis of bromoethylene at 163.3nm-
dc.title.alternative163.3nm에서 브로모에틸렌의 광분해 반응에 관한 연구-
dc.typeThesis(Master)-
dc.identifier.CNRN66577/325007-
dc.description.department한국과학기술원 : 화학과, -
dc.identifier.uid000871417-
dc.contributor.localauthorLee, Yoon-Sup-
dc.contributor.localauthor이윤섭-
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CH-Theses_Master(석사논문)
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