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Correlations between slow pyrolysis characteristics and organic carbon structure of aquatic plant biomass

机译:水生植物生物质慢热解特性与有机碳结构的相关性

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Thermal analysis techniques have been widely used to characterize natural organic matter; in particular, thermal oxidation has been used to examine soil and sediment organic matter. However, few studies have characterized natural organic matter (NOM) by using slow thermal degradation under a N-2 atmosphere. C-13 nuclear magnetic resonance (NMR) spectroscopy, UV-Vis spectroscopy, and three-dimensional excitation and emission matrix (EEM) fluorescence spectroscopy were used to characterize aquatic plant biomass for the detailed interpretation of the structures of organic carbon during slow pyrolysis. There was a significant linear correlation between the absorption of heat (99-110 degrees C) and the loss of mass (110-160 degrees C) (r(2)=0.507, p=0.01), which indicates that the initial slight loss in mass of the plant materials was due to the loss of less thermally stable components. The release of heat (277-311 degrees C) and the ratio of the specific absorbances at 253 and 203nm (A(253/203)) were also correlated (r(2)=0.388, p=0.008), which suggests that the release of plant biomass upon heating was associated with the proportion of substituent groups on aromatic rings and that the release of heat increased with the amount of substitution. The coefficient of determination (r(2)) between fulvic acid-like fluorescence peaks and the loss of mass (230-340 degrees C) was 0.236 (p=0.048). This result indicates that the loss of mass in the plant material samples was related to fulvic acid-like substances. More specifically, the reason for this result was the splitting of some aromatic functional groups, such as ether bonds, carbonyl groups, and oxygen heterocycles. In conclusion, these results suggest that the developed correlations between slow pyrolysis characteristics and organic carbon structures contribute to the investigation of the inner chemical structures of natural organic matter.
机译:热分析技术已广泛用于表征天然有机物;特别是,热氧化已经被用来检查土壤和沉积物的有机物质。然而,很少研究具有由N-2气氛下,用慢热降解特征的天然有机物质(NOM)。 C-13核磁共振(NMR)光谱,UV-Vis光谱,并三维激发和发射矩阵(EEM)荧光光谱进行了表征水生植物生物质为有机碳的结构的缓慢热解过程中的详细解释。有一个显著线性吸收热量之间(99-110℃)和质量损失(110-160℃)的相关性(R(2)= 0.507,P = 0.01),这表明初始轻微损失在植物材料的质量是由于更少的热稳定的成分的损失。释放热量(277-311℃)和特定的吸光度在253和203nm(A(203分之253))也相关联的比(r(2)= 0.388,P = 0.008),这表明在加热时的植物生物质的释放用的取代基的芳环上的比例和释放热量与置换量的增加有关。测定的黄腐酸样荧光峰和质量损失(230-340℃)之间的摩擦系数(R(2))为0.236(p值= 0.048)。该结果表明,物质的植物材料样品中的损失是有关黄腐酸样物质。更具体地,对于这种结果的原因是某些芳族官能团,如醚键,羰基和氧杂环的分裂。总之,这些结果表明,慢速热特性和有机碳结构之间的相互关系发展作出贡献的天然有机物质的内部化学结构的调查。

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