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紫外激光作用下环氧乙烷的TOF质谱研究

UV laser MPID time-of-f light mass spectra study on Oxirane

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【作者】 钱谊乐方黎郑海洋赵亚萍吴存恺余技广秦启宗

【Author】 QIAN YILE, FANG LI, ZHENG HAIYANG, ZHAO YAPING AND WU CUNKAI (Lab. of Laser Spectroscopy, Anhui Institute of Optics & Fine Mechanics, Academia Sinica, Hefei 230031)YU ZHIGUANG AND QIN QIZHONG(No. 2 Physics Department, Fu Dan University, Shanghai 200433) (Rece ived 24 December 1990; revised 7 March 1991)

【机构】 中国科学院安徽光机所激光光谱学实验室复旦大学物理二系复旦大学物理二系 合肥230031合肥230031上海200433上海200433

【摘要】 本文采用超声分子束技术,分别在308nm和355nm的紫外激光下,对环氧乙烷分子进行了多光子电离飞行时间(TOF)质谱研究.在308nm激光作用时,观测到C2H4O+、C2H3O+、CHO+和CH3+等离子的信号;在355nm激光作用时,则没有观测到分子离子的信号.在两种激光作用下最强的信号都是CHO+.但是两种激光下各碎片离子信号的光强指数有一定差别,表明在两种情形下,环氧乙烷分子经历了不同的电离解离过程.

【Abstract】 We studied the Multiphoton Ionization Dissociation (MPID) time-of-flight mass spectra of oxirane with ultrasonic molecular beam system at 308 nm and 355 nm laser radiation. In our experiments, the mass spectra distributions showed a certain extend of difference between two conditions. Under 355 nm laser radiation, there is no molecular ion signal and under 308nm we got a high laser intensity index for each fragment ions. Differing from electron impact ionization, the most intensive ion signal came from CHO+. With the laser intensity dependence of each fragment ion and its branch ratio we investigated the MPID process and mechanism of Oxirane at these two laser radiatios.

【基金】 国家自然科学基金
  • 【文献出处】 光学学报 ,Acta Optica Sinica , 编辑部邮箱 ,1992年01期
  • 【被引频次】6
  • 【下载频次】35
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