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Energy transfer between aromatic molecules was observed on a dielectric surface. The donor and acceptor molecules were vacuum deposited as bilayers and the surface temperature was linearly ramped in a temperature programmed desorption experiment (TPD). During the TPD procedure, the luminescence of the surface molecules was monitored as a function of temperature. Close to the desorption temperature of the lower layer, mixing of the layers occurred that resulted in energy transfer.  相似文献   
2.
甲基萘择型烷基化产物的毛细管气相色谱-质谱分析   总被引:2,自引:1,他引:2  
用色谱-质谱分析了在不同沸石分子筛催化剂上甲基萘择型烷基化产物组成及其含量;试用不同类型毛细管柱进行分析,找出最佳分析条件,共分离出26个峰,用面积归一化法测定其相对含量,并用气相色谱-质谱法对产物进行了鉴定。  相似文献   
3.
The alkylation of methylnaphthalene(MN) with methanol in the presence of HZSM-5 is a promising route for producing 2,6-dimetylnaphthalene(2,6-DMN) with a high selectivity. However, the conversion of MN is very low and the catalyst will be deactivated rapidly with increasing time on stream. In this study, the effects of the reaction pressure on the reactivity, selectivity and life of the catalyst of alkylation of MN over HZSM-5 modified by BaO were investigated. It was observed that with the enhancement of pressure, the conversion of MN increased, but the selectivity of 2,6-DMN kept unchanged, which was about 40% -42%. When the alkylation was carried out under a supercritical condition, the conversion of MN was 3-6 times higher and the life of catalyst was 25-30 times longer than those at an ambient pressure. The thermogravimetric analyses of the deactivated catalysts at different reaction pressures indicate that the amount of coke deposited on the catalysts was about 10% to 12 %, and the coke-burning reactions mainly took place in a temperature range from 720 to 860 K, and the apparent activation energies of the coke-burning catalysts at 0. 1 MPa( 10 h) and 7. 6 MPa( 108 h) were, respectively, 65.90 and 84. 72 kJ/mol. It is concluded from tile results that the supercritical condition is advantageous to enhancing the conversion of alkylation and extraction in situ, and to transporting those high molecular-weight poly-aromatic compounds so as to extend the catalyst life successively.  相似文献   
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