氨氧化法製備3

dc.contributor.author	洪志明	zh_tw
dc.date.accessioned	2014-10-27T15:23:54Z
dc.date.available	2014-10-27T15:23:54Z
dc.date.issued	1983-06-??	zh_TW
dc.description.abstract	3-Cyanopyridine is the intermediate for nicotinamidc and nicotinic acid. Benzonitrile is the intermediate for homosulfamine. A procedure has now been established for the laboratory fluidized-bed ammoxidation of 3-picoline and toluene to form 3-cyanopyridine in 35.2% yield and benzonitrile in 41.5% yield. The effects of reaction temperature, mole ratio of reactants, and amount of catalyst were studied.	en_US
dc.identifier	4D8F17C7-13B7-14B5-D1C3-D2E5D7BB8C18	zh_TW
dc.identifier.uri	http://rportal.lib.ntnu.edu.tw/handle/20.500.12235/17145
dc.language	中文	zh_TW
dc.publisher	國立臺灣師範大學研究發展處	zh_tw
dc.publisher	Office of Research and Development	en_US
dc.relation	(28)，609-624	zh_TW
dc.relation.ispartof	師大學報	zh_tw
dc.subject.other	苯甲腈	zh_tw
dc.subject.other	氨氧化法	zh_tw
dc.subject.other	啶	zh_tw
dc.title	氨氧化法製備3	zh-tw
dc.title.alternative	Preparation of 3-Cyanopyridine and Benzonitrile by Ammoxidation	zh_tw

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