利用碳化硅压腔在常压至1.5GPa和26℃条件下对液态2-甲基戊烷进行了拉曼光谱测量,讨论了C-H拉曼峰频率、强度、面积、以及谱峰宽度随压力升高的变化规律。实验结果表明,2-甲基戊烷的拉曼位移在2800-3000cm。范围内的CH。和cH。的伸缩振动谱峰随着压力的增大均连续向高波数位移,其拉曼位移与压力的关系可以表示为Vas(CH3)=O.0131p+2960.1,Vs(CH3)=0.0088p+2871.0,vas(CH2)-0.0089p+2930.2,%。(CH2)’=0.007Op+2903.1和vs(CH2)=000079p+2844.7。另外处理实验结果时发现,在0~1.5GPa条件下,2-甲基戊烷的Vas(CH3)拉曼位移可以进行压力标定,其方程为:P(MPa)=76.2(△vp)2960+21.65(r^2=0.9958)。该压力体标定剂,适合于不希望有Si和Al等元素出现的体系。
The present paper investigates the Raman spectral character of liquid 2-methylpentane by an experiment at the pressure of 0-1.5 GPa and the temperature of 26 ℃, and defines the relation between the pressure and the Raman peak of 2-methylpentane at ambient temperature. The result shows that there are five characteristic Raman peaks in 2-methylpentane defined as v (CH2) and v(CH3 ), and all of them move to high position as the system pressure increases. 1 ne relation between the system pressure and peaks positions is given as following: vss (CH3)=0. 013 1p+2 960. 1, vs (CH3)=0. 008 8p+2 871.0, vas (CH2)= 0. 008 9p+2 930. 2, vas(CH2) '=0. 007 0p+2 903 and vs(CH2) =0. 007 9p+2 844.7. On the other hand, 2-methylpentane is reliable as a liquid pressure gauge for high pressure experiment. The equation applied to demarcate system pressure is also showed: p(MPa)=76. 2(△vp)2 960+21.65(r^2 =0. 995 8). This is probably the first organic liquid gauge, especially for systems not expected to emergence of Si, Al and hydroxyl matter.