化学学报 ›› 2013, Vol. 71 ›› Issue (01): 88-92.DOI: 10.6023/A12110873 上一篇    下一篇

研究论文

乙苯与二甲苯在超临界压力下的热裂解研究

王丹丹a, 巩春明a, 朱权a, 王健礼b, 李象远a   

  1. a 四川大学化工学院 成都 610065;
    b 四川大学化学学院 成都 610065
  • 投稿日期:2012-11-05 发布日期:2012-12-18
  • 通讯作者: 朱权, 李象远 E-mail:qzhu@scu.edu.cn; xyli@scu.edu.cn
  • 基金资助:
    项目受国家自然科学基金(Nos. 91116001/A0204, 91216119)资助.

Study for Pyrolysis of Ethylbenzene and Xylene under Supercritical Pressure

Wang Dandana, Gong Chunminga, Zhu Quana, Wang Jianlib, Li Xiangyuana   

  1. a College of Chemical Engineering, Sichuan University, Chengdu 610065;
    b College of Chemistry, Sichuan University, Chengdu 610065
  • Received:2012-11-05 Published:2012-12-18
  • Supported by:
    Project supported by the National Natural Science Foundation of China (Nos. 91116001/A0204, 91216119).

采用连续流动装置, 在压力为4 MPa, 温度分别在700, 750和780 ℃条件下, 开展了乙苯和二甲苯在超临界压力条件下热裂解反应的实验研究. 对乙苯和二甲苯裂解的气相产物, 采用在线气相色谱进行分析; 而裂解的液相产物则通过色质联用仪进行定量分析. 研究发现乙苯和二甲苯裂解的气相产物组成基本相同, 而液相产物组成相差较大, 但都是芳香烃类化合物. 乙苯和二甲苯的转化率都随温度升高而增加; 在相同温度下, 乙苯比二甲苯转化率高. 此外, 裂解过程并未发现明显的结焦现象, 说明纯芳香烃物质的热裂解并不会导致严重积炭. 同时, 本文还采用密度泛函方法在BHandHLYP/6-31+G(d, p)水平上, 对乙苯和甲苯分别进行结构优化并计算相关的键能. 计算结果表明: 乙苯侧链乙基中的C—C键的键能最小, 从而说明乙苯侧链烷基更容易发生断键反应, 理论结果很好地解释了乙苯比二甲苯裂解转化率高的实验现象. 本文的工作对燃料裂解结焦机理的重新认识有重要的意义.

关键词: 乙苯, 二甲苯, 热裂解, 超临界, 结焦, 键能

Under the supercritical pressure, the pyrolysis reactions of ethylbenzene and xylene were investigated by using the continuous flow device. At the pressure of 4 MPa and the different temperatures of 700, 750 and 780 ℃, the pyrolysis gaseous products were analyzed by online gas chromatography for ethylbenzene and xylene, while their liquid products were quantitatively analyzed by gas chromatography-mass spectrometry (GC-MS). It is found that the gaseous products of ethylbenzene decomposition are similar to those of xylene, while the liquid products of ethylbenzene and xylene decomposition are quite different, of which the major products are aromatic hydrocarbons. The experiment reveals that the higher the pyrolysis temperature is, the higher the conversion ratio will be for ethylbenzene and xylene. On the other hand, the conversion ratio of ethylbenzene is higher than that of xylene at the same temperature in experiment. From the experimental observation, we conclude that the pure aromatic hydrocarbon does not cause serious coking during the cracking process, owing to the low pyrolysis. Theoretical calculations are performed to obtain the bond energies for the different C—C or C—H bond types in side alkyl groups of ethylbenzene and xylene, by using density functional theory (DFT) method at the BHandHLYP/6-31+G(d, p) level. The bond energies calculated in this study agree well with those available from literature. It is found that the weakest bond is the C—C bond in the ethyl group of ethylbenzene, with a bond energy of 313.1 kJ/mol. This value is much smaller than the smallest bond energy of 393.2 kJ/mol of the C—H bond in the substituted methyl group in xylene. The weakness of the C—C bond in ethylbenzene thus leads to the fact that the pyrolysis of ethylbenzene is much easier than that of xylene. The theoretical results predict a higher conversion ratio of ethylbenzene than that of xylene. So the calculation gives a good explanation for the experimental phenomenon. Finally, the study in this work shows a new and important insight to the coking mechanism for the hydrocarbon fuels.

Key words: ethylbenzene, xylene, pyrolysis, supercritical, coke, bond energy