基于木质素生物炭的碳热合成、嵌入和表面沉积纳米零价铁复合材料:材料特性比较、选择性气体吸附和硝基芳烃修复

Yasmitha A. Alahakoon , Shine C. Wilson , Chathuri Peiris , Yohara K. Ranasinghe , Sameera R. Gunatilake , Xuefeng Zhang , Todd E. Mlsna , Upul Kumarasinghe , M.Infas H Mohideen , Upendar Reddy Gandra , Anish Mathai Varghese , Georgios N. Karanikolos , Dinesh Mohan
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引用次数: 0

摘要

掺入纳米级零价铁(nZVI)的生物炭(BC)为水净化提供了有利的材料。虽然最常见的 nZVI 添加方法是沉积在载体表面,但也有报道称将其嵌入支持基质中。然而,目前还没有对嵌入材料在去除污染物方面的行为进行充分研究,也没有对这两种材料的特性和修复能力进行比较。本研究的重点是制备和广泛表征两种材料:嵌入(Lig-e-nZVI)木质素 BC 中的 nZVI 和表面沉积(Lig-s-nZVI)木质素 BC,然后对两种硝基芳香族化合物(对硝基苯胺(pNA)和对硝基苯酚(pNP))的修复作用进行比较研究。Lig-e-nZVI 和 Lig-s-nZVI 的合成分别涉及木质素的同步热解和铁盐的碳热还原。Lig-e-nZVI 显示出更高的孔隙率。XRD 证实了 Fe0 的形成。HR-TEM 图像证明了 nZVI 的核壳结构,0.36 nm 的壳层间距证实了 Fe0 颗粒被石墨烯包裹,同时还观察到碳化铁内层,Lig-e-nZVI 的碳化铁内层较薄,而 Lig-s-nZVI 的碳化铁内层较厚。2.54 eV 的带隙能表明这两种材料都具有光催化活性。最佳拟合 Sips 等温线显示,Lig-s-nZVI 对 pNP 和 pNA 的吸附容量分别为 23.1 和 13.1 mg g-1。在 4 个再生周期中,Lig-e-nZVI 的稳定性最高。所开发材料的物理化学特征进一步实现了对气体的选择性吸附。这些研究结果为了解不同合成的 nZVI-BC 复合材料的理化特性和补救作用提供了新的视角。
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Carbothermally synthesized, lignin biochar-based, embedded and surface deposited nano zero-valent iron composites: Comparative material characterization, selective gas adsorption and nitroaromatics remediation
Biochar (BC) with nanoscale zero-valent iron (nZVI) incorporation offers advantageous materials for water purification. While the most common approach for nZVI incorporation is the deposition on -a carrier surface, embedding in -a support matrix has also been reported. However, the behavior of the embedded material in contaminant removal has not been adequately studied -nor the characteristics and the remediation capabilities of the two materials have been compared. Present study focuses on preparing and extensively characterizing two materials: nZVI embedded in (Lig-e-nZVI) and surface deposited on (Lig-s-nZVI) lignin BC followed by a comparative study of remedial action for two nitroaromatics, p-nitroaniline (pNA) and p-nitrophenol (pNP). The synthesis of Lig-e-nZVI and Lig-s-nZVI involved simultaneous and subsequent pyrolysis of lignin and carbothermal reduction of the iron salt, respectively. Lig-e-nZVI showed enhanced porosity. XRD confirmed the formation of Fe0. HR-TEM images proved the core-shell structure of nZVI, and an interlayer spacing of 0.36 nm of the shell verified that the Fe0 particles were encapsulated with graphene while an iron carbide inner layer was also observed, thinner in Lig-e-nZVI and thicker in Lig-s-nZVI. A band gap energy of 2.54 eV suggested photocatalytic activity for both materials. Best fitted Sips isotherms showed 23.1 and 13.1 mg g−1 capacities for Lig-s-nZVI in pNP and pNA adsorption respectively. Highest stability was portrayed by Lig-e-nZVI over 4 regeneration cycles. The physicochemical features of the developed materials further enabled selective gas adsorption. Findings provide new insights into physicochemical characteristics and remedial actions of differently synthesized nZVI-BC composites.
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