[Using instantaneous spectra to determine dominant species in the DDT process of epoxypropane].

After solving problems of weak light detection, the calibration of the spectral sensitivity of the measuring system, and the synchronization of the measuring system, instantaneous emission spectra of epoxypropane in the process of deflagration to detonation transition (DDT) with the exposure time of 2-8 micros and the resolution of 0. 2 nm were acquired from six different side windows of an explosion shock tube. Using the corrected spectral data, curves of the optical radiant intensity of main reaction products versus the DDT distance from the ignition point were obtained. These curves provided information about the evolution of the reaction and the products during the DDT process. Results indicate that the chemical reaction rate of the gaseous fuel and the corresponding concentrations of intermediate products increased gradually at the deflagration stage, but at the moment of deflagration to detonation transition, the reaction rate increased rapidly and the concentrations! of products increased sharply. Among these main products, concentration increments of molecule CO, and radicals CHO and OH were greater than other products, which means that CO, CHO and OH are the dominant species that affect the DDT process greatly.

[The measurement and analysis of visible-absorption spectrum and fluorescence spectrum of lycopene].

Using ICCD spectral detection system, the absorbency of lycopene-carbon bisulfide solution with different concentration was measured, and the result shows that in a specified range the absorption rule of lycopene solution agrees with Lambert-Beer Law. Absorption spectral wavelength shifts were measured respectively when lycopene was dissolved in acetone, normal hexane, petroleum ether, benzene, ethyl acetate, and carbon bisulfide, and comparing to acetone, different red-shift appeared when lycopene was dissolved in benzene, ethyl acetate, and carbon bisulfide when water was added in lycopene-acetone solution, t he absorbency of lycopene dropped, the fine structure of absorption spectrum became indistinct, and a new absorption peak appeared in UV. The reason for these phenomena is that the solvent molecule had different effect on lycopene molecule when lycopene was dissolved in different solvent. Using fluorecence spectrophotometer, fluorescence spectra of lycopene in different concentrations were collected, and the results show that the fluorescence spectra of lycopene were mainly in 500-680 nm. When concentration was lower than 50 microg x mL(-1), the fluorescence intensity linearly increased with increasing concentration, and when concentration was higher than 60 microg x mL(-1), the fluorescence intensity dropped because of the interaction between lycopene molecules.