Biochemical and Environmental Engineering Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India.
Biochemical and Environmental Engineering Laboratory, Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, Assam, 781039, India.
Environ Res. 2024 Nov 1;260:119579. doi: 10.1016/j.envres.2024.119579. Epub 2024 Jul 8.
In this work, a novel nitrogen-doped biochar bentonite composite was synthesized by a single-pot co-pyrolysis method. Batch studies were conducted to evaluate the performance of the developed composite in eliminating synthetic dyes from the aqueous matrix. Energy dispersive X-ray spectroscopy analysis and field emission scanning electron microscopy imaging confirmed the N doping and bentonite impregnation into biochar. X-ray photoelectron spectroscopy analysis revealed that the N atoms were doped interstitially into the carbon matrix of biochar in the form of pyridinic and pyrrolic nitrogen. Simultaneous heteroatom doping and bentonite impregnation reduced the specific surface area to 41.721 m g but improved the adsorption capacity of biochar for dye adsorption. Further experimental studies depicted that simultaneous bentonite impregnation and N doping into the biochar matrix is beneficial for direct blue-6 (DB-6) and methylene blue (MB) removal and maximum adsorption capacities of 53.17 mg. g and 41.33 mg. g were obtained for MB and DB-6, respectively, at varying conditions. Adsorption energetics of the dyes with the developed composite portrayed the spontaneity of the process through negative ΔG values. The Langmuir and Freundlich isotherm models fitted the best for MB and DB-6 adsorption. The monolayer adsorption capacity and favourability factor for MB and DB-6 adsorption were calculated to be 54.15 mg. g and 0.217, respectively from the best-fitted isotherms. Based on density functional theory calculations and spectroscopic studies, major interactions governing the adsorption were predicted to be charge-based interactions, π-π interactions, H-bonding, and Lewis acid-base interactions.
在这项工作中,通过一锅共热解方法合成了一种新型氮掺杂生物炭膨润土复合材料。进行了批处理研究,以评估开发的复合材料在从水基质中消除合成染料方面的性能。能量色散 X 射线光谱分析和场发射扫描电子显微镜成像证实了 N 掺杂和膨润土浸渍到生物炭中。X 射线光电子能谱分析表明,N 原子以吡啶氮和吡咯氮的形式间隙掺杂到生物炭的碳基质中。同时进行杂原子掺杂和膨润土浸渍会将比表面积降低到 41.721 m2/g,但会提高生物炭对染料吸附的吸附容量。进一步的实验研究表明,同时将膨润土浸渍和 N 掺杂到生物炭基质中有利于直接蓝 6(DB-6)和亚甲蓝(MB)的去除,并且在不同条件下,MB 和 DB-6 的最大吸附容量分别为 53.17 mg·g-1和 41.33 mg·g-1。染料与开发复合材料的吸附能谱通过负的 ΔG 值描绘了该过程的自发性。Langmuir 和 Freundlich 等温线模型最适合 MB 和 DB-6 的吸附。从最佳拟合的等温线计算出 MB 和 DB-6 吸附的单层吸附容量和有利因子分别为 54.15 mg·g-1和 0.217。基于密度泛函理论计算和光谱研究,预测控制吸附的主要相互作用是基于电荷的相互作用、π-π 相互作用、氢键和路易斯酸碱相互作用。