Papadopoulou Katerina, Tarani Evangelia, Ainali Nina Maria, Chrissafis Konstantinos, Wurzer Christian, Mašek Ondřej, Bikiaris Dimitrios N
Laboratory of Polymer Chemistry and Technology, Department of Chemistry, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece.
Laboratory of Advanced Materials and Devices, Department of Physics, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece.
Molecules. 2023 Jul 11;28(14):5330. doi: 10.3390/molecules28145330.
In the present study, poly(butylene succinate) (PBSu) and its bionanocomposites containing 1, 2.5, and 5 wt.% biochar (MSP700) were prepared via in situ melt polycondensation in order to investigate the thermal stability and decomposition mechanism of the materials. X-ray photoelectron spectroscopy (XPS) measurements were carried out to analyze the surface area of a biochar sample and PBSu/biochar nanocomposites. From XPS, it was found that only physical interactions were taking place between PBSu matrix and biochar nanoadditive. Thermal stability, decomposition kinetics, and the decomposition mechanism of the pristine PBSu and PBSu/biochar nanocomposites were thoroughly studied by thermogravimetric analysis (TGA) and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). TGA thermograms depicted that all materials had high thermal stability, since their decomposition started at around 300 °C. However, results indicated a slight reduction in the thermal stability of the PBSu biochar nanocomposites because of the potential catalytic impact of biochar. Py-GC/MS analysis was employed to examine, in more detail, the thermal degradation mechanism of PBSu nanocomposites filled with biochar. From the decomposition products identified by Py-GC/MS after pyrolysis at 450 °C, it was found that the decomposition pathway of the PBSu/biochar nanocomposites took place mainly via β-hydrogen bond scission, which is similar to that which took place for neat PBSu. However, at higher biochar content (5 wt.%), some localized differences in the intensity of the peaks of some specific thermal degradation products could be recognized, indicating that α-hydrogen bond scission was also taking place. A study of the thermal stability and decomposition pathway of PBSu/biochar bionanocomposites is crucial to examine if the new materials fulfill the requirements for further investigation for mulch films in agriculture or in electronics as possible applications.
在本研究中,通过原位熔融缩聚制备了聚丁二酸丁二醇酯(PBSu)及其含有1 wt.%、2.5 wt.%和5 wt.%生物炭(MSP700)的生物纳米复合材料,以研究材料的热稳定性和分解机理。进行了X射线光电子能谱(XPS)测量,以分析生物炭样品和PBSu/生物炭纳米复合材料的表面积。通过XPS发现,PBSu基体与生物炭纳米添加剂之间仅发生物理相互作用。通过热重分析(TGA)和热解气相色谱/质谱联用(Py-GC/MS)对原始PBSu和PBSu/生物炭纳米复合材料的热稳定性、分解动力学和分解机理进行了深入研究。TGA热重曲线表明,所有材料都具有较高的热稳定性,因为它们在约300℃开始分解。然而,结果表明,由于生物炭的潜在催化作用,PBSu生物炭纳米复合材料的热稳定性略有降低。采用Py-GC/MS分析更详细地研究了填充生物炭的PBSu纳米复合材料的热降解机理。从450℃热解后Py-GC/MS鉴定出的分解产物中发现,PBSu/生物炭纳米复合材料的分解途径主要通过β-氢键断裂发生,这与纯PBSu的分解途径相似。然而,在较高的生物炭含量(5 wt.%)下,可以识别出一些特定热降解产物峰强度的局部差异,表明也发生了α-氢键断裂。研究PBSu/生物炭生物纳米复合材料的热稳定性和分解途径对于检验这些新材料是否满足作为农业或电子领域地膜进一步研究的要求至关重要,这些领域可能是其潜在应用领域。