School of Environment and Energy, South China University of Technology, Guangzhou 510006, PR China.
College of Environmental Science and Engineering, Guangdong University of Petrochemical Technology, Maoming 525000, PR China.
Sci Total Environ. 2021 May 10;768:144281. doi: 10.1016/j.scitotenv.2020.144281. Epub 2020 Dec 31.
Owing to its environmental-friendliness, low-cost, and outstanding characteristics, biochar has been widely used for the catalytic degradation of various organic pollutants. In this study, a pre- and post-deashing graphitized biochar (DBC800 and PBC800-A) was prepared and compared with the pristine biochar (PBC800) to activate persulfate (PS) for tetracycline (TC) degradation. The influence of the natural endogenous mineral on the catalytic ability of biochar was investigated. Characterization results show that the inherent endogenous mineral in biochar not only acted as a natural pore-forming agent to promote the formation of the porous structure, but also facilitated the formation of edge defective structures, and altered the surface functional groups, as well as increased the carbonization and graphitization degree of biochar. The PBC800-A exhibited a much higher catalytic efficiency on PS activation and TC oxidative degradation with the reaction rate of 0.06055 min, 7.14 times as that of DBC800 (0.00861 min) and 4.63 times as that of PBC800 (0.00158 min). The endogenous minerals were conducive to the generation of free radicals and promoted the oxidative degradation of TC, which was mainly attributed to the improved carbon configuration. The post-deashing treatment was also found to significantly improve the electron transport efficiency of biochar by removing the residual ash, thereby promoting the generation of singlet oxygen. This study demonstrated that the natural minerals in biochar was beneficial for the degradation of TC, and more alternative natural minerals can be applied to co-pyrolysis with biochar for the remediation of refractory organic pollutants.
由于生物炭具有环境友好、成本低和突出的特点,因此已被广泛用于催化降解各种有机污染物。在本研究中,制备了预除灰和后除灰的石墨化生物炭(DBC800 和 PBC800-A),并与原始生物炭(PBC800)进行了比较,以激活过硫酸盐(PS)降解四环素(TC)。研究了天然内源性矿物质对生物炭催化能力的影响。表征结果表明,生物炭中的固有内源性矿物质不仅充当了天然成孔剂以促进多孔结构的形成,而且还促进了边缘缺陷结构的形成,并改变了表面官能团,同时增加了生物炭的碳化和石墨化程度。PBC800-A 在 PS 活化和 TC 氧化降解方面表现出更高的催化效率,反应速率为 0.06055 min,是 DBC800(0.00861 min)的 7.14 倍,是 PBC800(0.00158 min)的 4.63 倍。内源性矿物质有利于自由基的生成,并促进了 TC 的氧化降解,这主要归因于改善的碳结构。还发现后除灰处理通过去除残留灰分,显著提高了生物炭的电子传输效率,从而促进了单线态氧的生成。本研究表明,生物炭中的天然矿物质有利于 TC 的降解,并且可以应用更多替代的天然矿物质与生物炭共热解,用于修复难处理的有机污染物。