在线热解-光电离质谱法研究Li2CO3对松木热解的影响

On-line Study on the Catalytic Pyrolysis of Pine Wood over Li2CO3 Using Pyrolysis-Photoionization Mass Spectrometry

  • 摘要: 利用热重分析结合在线热解-光电离质谱法研究了Li2CO3对松木催化热解过程的影响。热重分析结果表明,Li2CO3的掺入能够使松木热解向低温区移动,且不会显著增加焦炭的产量。在线热解-光电离质谱研究结果表明,松木的3种组分,纤维素、半纤维素和木质素,对催化剂Li2CO3的响应不同:纤维素和半纤维素主要热解产物产量有下降趋势,而木质素主要热解产物产量却明显上升;松木主要热解产物的最大生成速率时间和温度都有不同程度的减小。本实验结果表明,热解产物对催化剂的不同响应与它们自身结构有密切关系,在松木热解过程中,Li+能降低含氧热解产物的C—O键能从而促进裂解。

     

    Abstract: The catalytic effect of Li2CO3 on pine wood pyrolysis was studied by thermogravimetry (TG) and homemade pyrolysis-photoionization mass spectrometry (Py/PI-MS). The TG and derivative thermogravimetry (DTG) curves indicated that the pyrolysis temperature of pine wood was reduced and the yield of coke didn’t increase significantly in the presence of Li2CO3. The DTG curve of pure pine wood was characterized by a shoulder peak. Since the pyrolysis temperature of hemicellulose was lower than that of cellulose, the peak and shoulder peak were mainly attributed to the decomposition of cellulose and hemicellulose, respectively. The shoulder peak in the DTG curve of pine wood/Li2CO3 disappeared, indicating the pyrolysis temperature of cellulose was reduced obviously and the pyrolysis temperature of hemicellulose decreased slightly.
    Py/PI-MS is an on-line analytical method which combines pyrolysis furnace with photoionization mass spectrometry. Thanks to the “soft” ionization method (10.6 eV), nearly few or no fragments are produced in the mass spectra. The experiment was carried out in two modes: (1) In temperature-fixed mode, the mass spectra of pine wood and pine wood/Li2CO3 pyrolyzates at different temperatures as well as the time-evolved profiles were obtained. (2) In temperature-programmed mode, the temperature-evolved profiles of pine wood and pine wood/Li2CO3 pyrolyzates were obtained. The results of Py/PI-MS showed that the three primary components of pine wood, i.e., cellulose, hemicellulose and lignin had different responses to the added catalyst, Li2CO3. The yield of pyrolyzates from cellulose and hemicellulose were decreased, while pyrolyzates yields from lignin increased significantly. From time-evolved profiles, the time to reach the maximum reaction rate of pyrolyzates were advanced in the presence of Li2CO3. From temperature-evolved profiles, the temperature to reach the maximum reaction rate of pyrolyzates were advanced due to added Li2CO3. The major pyrolysis products of hemicellulose had only one peak, which was consistent with their generation paths. The pyrolysis products of cellulose and lignin had two peaks, indicating that they had multiple different generation paths, which were also consistent with their generation paths. As mentioned above, Li2CO3 had a profound effect upon the pyrolysis of pine wood. It has been investigated by considering the effect of Li+ on the reaction energy barrier for the decomposition of pyrolyzates. The possible catalytic mechanism was proposed that the bond energy of C—O of pyrolyzates were reduced in the presence of Li+, thus promoting the decomposition of pyrolyzates. Pine wood pyrolyzates showed different responses to the catalyst, which were closely related to their different structures. This work provides the basis for the research of biomass catalytic pyrolysis mechanism and the potential of industrial application.

     

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