Zhang Jinhong, Sekyere Daniel T, Niwamanya Noah, Huang Yansheng, Barigye Andrew, Tian Yuanyu
State Key Laboratory of Heavy Oil Processing, College of Chemical Engineering, China University of Petroleum, Qingdao 266580, China.
Shandong Engineering and Technology Research Center of High Carbon Energy Low Carbonization, China University of Petroleum, Qingdao 266580, China.
ACS Omega. 2022 Jan 25;7(5):4245-4256. doi: 10.1021/acsomega.1c05907. eCollection 2022 Feb 8.
To understand the fast pyrolysis kinetics and product evolution of waste pine sawdust, high heating rate thermogravimetry-Fourier transform infrared (TG-FTIR) was used to obtain the kinetic parameters and the chemical groups formed during the pyrolysis process, while pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) was used to investigate the detailed compositions of products under the staged (seven stages from 300 to 600 °C) and direct fast pyrolysis process. Spectral bands were identified for acids, alcohols, aldehydes, aromatics, esters, ethers, hydrocarbons, ketones, phenols, and sugars. Research found that the apparent activation energy for fast pyrolysis is much higher than that of slow pyrolysis. The evolution of CO is the major deoxygenation route. Cracking mainly occurred at the 450 °C stage with phenols, ketones, aldehydes, and sugars as the main products. The product distributions for different stages are significantly different; the selectivity of aldehydes decreased, while phenols showed an upward trend with an increase in pyrolysis temperature. Ketones and sugars reached their peak values at 450 °C. The changes in the molecular composition of each stage helped to understand the pyrolysis process. Compared with the staged pyrolysis, the direct pyrolysis process had higher selectivity of acids, aldehydes, esters, and sugars and lower selectivity of phenols, ketones, and alcohols.
为了解废弃松木锯末的快速热解动力学和产物演变,采用高升温速率热重-傅里叶变换红外光谱联用仪(TG-FTIR)获取热解过程中的动力学参数和形成的化学基团,同时采用热解-气相色谱/质谱联用仪(Py-GC/MS)研究分段(300至600℃的七个阶段)和直接快速热解过程下产物的详细组成。确定了酸、醇、醛、芳烃、酯、醚、烃、酮、酚和糖的光谱带。研究发现,快速热解的表观活化能远高于慢速热解。CO的演变是主要的脱氧途径。裂解主要发生在450℃阶段,主要产物为酚、酮、醛和糖。不同阶段的产物分布有显著差异;随着热解温度的升高,醛的选择性降低,而酚呈上升趋势。酮和糖在450℃达到峰值。各阶段分子组成的变化有助于理解热解过程。与分段热解相比,直接热解过程中酸、醛、酯和糖的选择性较高,而酚、酮和醇的选择性较低。