Nair Rahul Ramesh, Kißling Patrick A, Schaate Andreas, Marchanka Alexander, Shamsuyeva Madina, Behrens Peter, Weichgrebe Dirk
Institute of Sanitary Engineering and Waste Management (ISAH), Leibniz University of Hannover Hannover 30167 Germany
Institute of Physical Chemistry and Electrochemistry (PCI), Leibniz University of Hannover Hannover 30167 Germany.
RSC Adv. 2023 May 2;13(20):13526-13539. doi: 10.1039/d3ra01911j.
The porous non-graphitizing carbon (NGC) known as biochar is derived from the pyrolytic conversion of organic precursors and is widely investigated due to its multifunctional applications. At present, biochar is predominantly synthesized in custom lab-scale reactors (LSRs) to determine the properties of carbon, while a thermogravimetric reactor (TG) is utilized for pyrolysis characterization. This results in inconsistencies in the correlation between the structure of biochar carbon and the pyrolysis process. If a TG reactor can also be used as an LSR for biochar synthesis, then the process characteristics and the properties of the synthesized NGC can be simultaneously investigated. It also eliminates the need for expensive LSRs in the laboratory, improves the reproducibility, and correlatability of pyrolysis characteristics with the properties of the resulting biochar carbon. Furthermore, despite numerous TG studies on the kinetics and characterization of biomass pyrolysis, none have questioned how the properties of biochar carbon vary due to the influence of the starting sample mass (scaling) in the reactor. Herein, with a lignin-rich model substrate (walnut shells), TG is utilized as an LSR, for the first time, to investigate the scaling effect starting from the pure kinetic regime (KR). The changes in the pyrolysis characteristics and the structural properties of the resultant NGC with scaling are concurrently traced and comprehensively studied. It is conclusively proven that scaling influences the pyrolysis process and the NGC structure. There is a gradual shift in pyrolysis characteristics and NGC properties from the KR until an inflection mass of ∼200 mg is reached. After this, the carbon properties (aryl-C%, pore characteristics, defects in nanostructure, and biochar yield) are similar. At small scales (≲100 mg), and especially near the KR (≤10 mg) carbonization is higher despite the reduced char formation reaction. The pyrolysis is more endothermic near KR with increased emissions of CO and HO. For a lignin-rich precursor, at masses above inflection point, TG can be employed for concurrent pyrolysis characterization and biochar synthesis for application-specific NGC investigations.
被称为生物炭的多孔非石墨化碳(NGC)源自有机前驱体的热解转化,因其多功能应用而受到广泛研究。目前,生物炭主要在定制的实验室规模反应器(LSR)中合成,以确定碳的性质,而热重反应器(TG)则用于热解表征。这导致生物炭碳结构与热解过程之间的相关性不一致。如果TG反应器也可以用作生物炭合成的LSR,那么就可以同时研究合成过程的特性和所得NGC的性质。这也消除了实验室中对昂贵LSR的需求,提高了热解特性与所得生物炭碳性质之间的可重复性和相关性。此外,尽管有许多关于生物质热解动力学和表征的TG研究,但没有人质疑生物炭碳的性质如何因反应器中起始样品质量(规模)的影响而变化。在此,以富含木质素的模型底物(核桃壳)为例,首次将TG用作LSR,从纯动力学区域(KR)开始研究规模效应。同时追踪并全面研究了随着规模变化,所得NGC的热解特性和结构性质的变化。最终证明规模会影响热解过程和NGC结构。从KR开始,热解特性和NGC性质会逐渐发生变化,直到达到约200 mg的拐点质量。在此之后,碳性质(芳基-C%、孔隙特征、纳米结构缺陷和生物炭产率)相似。在小规模(≲100 mg)下,尤其是在接近KR(≤10 mg)时,尽管炭形成反应减少,但碳化程度更高。在KR附近,热解更吸热,同时CO和HO的排放量增加。对于富含木质素的前驱体,在质量高于拐点时,TG可用于同时进行热解表征和生物炭合成,以进行特定应用的NGC研究。