摘要
制备了硫酸镍固体材料.采用红外光谱(IR)、程序升温脱附(TPD)和激光促进表面反应(LSSR)技术,研究了乙烯在NiSO4表面上的化学吸附态和激光促进C2H4表面反应性能.实验结果表明,C2H4以H原子与固体材料表面Lewis碱位(S=O键中的端氧)作用,形成分子吸附态.在常压和 100℃条件下,用 1079 cm-1激光激发吸附有C2H4分子中H的S=O键100次,C2H4转化率可达15%,生成丁二烯的选择性为100%.根据表征和反应结果,讨论了C2H4在NiSO4上的LSSR机理和影响LSSR性能的因素.
Solid material NiSO4 was prepared. A TEA-CO2 laser generator was adopted as the light source to carry on laser stimulated surface coupling reaction of ethylene. The infrared vibration structure and adsorption state of C2H4ad--NiSO4 system were discussed based on infrared and temperature programmed desorption tests. It was showed that C2H4 is adsorbed as molecular state, bonding with NiSO4 surface through H atom at terminal O of S =O. The 1 079 cm-1 laser was selected to activate solid surfacial bond S =O, which absorbs the photon energy efficiently. At normal pressure and a temperature below 100 ℃, C2H4 conversed to butadiene with a high selectivity of 100%. Increasing laser pulse can improve conversion of C2H4 without change of selectivity. After 200 pulses, C2H4 in the system had been consumed to a large extent, and the product occupied most of the surface active sites, therefore conversion of C2H4 increased at a low speed. Temperature can also affect the laser stim-ulated surface reaction of C2H4ad-NiSO4. At 100 ℃, 15. 1% of C2H4 convert to butadiene, while keeping high selectivity of 100%. Based on the above experimental results, a mechanism of LSSR was proposed for the conversion of C2H4 to C4H6.
出处
《物理化学学报》
SCIE
CAS
CSCD
北大核心
2001年第10期936-939,共4页
Acta Physico-Chimica Sinica
基金
教育部博士点基金资助项目