Green Synthesis of De Novo Bioinspired Porous Iron-Tannate Microstructures with Amphoteric Surface Properties

H. Rathnayake, Sheeba Dawood, G. Pathiraja, Kelvin Adrah, Olubunmi O. Ayodele
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引用次数: 4

Abstract

Bioinspired porous microstructures of iron-tannate (Fe(III)-TA) coordination polymer framework were synthesized by catenating natural tannic acid with iron(II), using a scalable aqueous synthesis method in ambient conditions. The chemical composition, morphology, physiochemical properties, and colloidal stability of microstructures were elucidated. The surface area (SBET) and the desorption pore volume were measured to be 70.47 m2/g and 0. 44 cm3/g, respectively, and the porous structure was confirmed with an average pore dimension of ~27 nm. Microstructures were thermally stable up to 180 °C, with an initial weight loss of 13.7% at 180 °C. They exhibited high chemical stability with pH-responsive amphoteric properties in aqueous media at pH levels ranging from 2 to 12. Supporting their amphoteric sorption, microstructures exhibited rapid removal of Pb+2 from water, with 99% removal efficiency, yielding a maximum sorption capacity of 166.66 mg/g. Amphoteric microstructures of bioinspired metal–phenolate coordination polymers remain largely unexplored. Additionally, natural polyphenols have seldomly been used as polytopic linkers to construct both porous and pH-responsive amphoteric coordination polymer frameworks with a robust structure in both acidic and basic media. Thus, this de novo porous microstructure of Fe(III)-TA and its physiochemical surface properties have opened new avenues to design thermally and chemically stable, eco-friendly, low-cost amphoteric sorbents with multifunctionality for adsorption, ion exchange, separation, storage, and sensing of both anions and cations present in heterogeneous media.
绿色合成具有两性表面特性的新型多孔单宁酸铁微结构
以天然单宁酸和铁(II)为催化剂,采用可扩展的水相合成方法,在环境条件下合成了铁-丹酸铁(Fe(III)-TA)配位聚合物框架的仿生多孔结构。分析了微观结构的化学组成、形态、理化性质和胶体稳定性。测得的比表面积(SBET)和解吸孔体积分别为70.47 m2/g和0。为44 cm3/g,确定了孔隙结构,平均孔径为~27 nm。显微组织在180°C时热稳定,180°C时的初始重量损失为13.7%。在pH值为2 ~ 12的水介质中,它们表现出高度的化学稳定性和pH响应两性性质。支持其两性吸附的微观结构对水中Pb+2的快速去除,去除效率为99%,最大吸附量为166.66 mg/g。生物激发金属-酚酸盐配位聚合物的两性微观结构仍未被广泛探索。此外,在酸性和碱性介质中,天然多酚很少被用作多聚体连接剂来构建具有坚固结构的多孔性和ph响应性两性配位聚合物框架。因此,这种全新的Fe(III)-TA的多孔结构及其物理化学表面特性为设计热稳定性和化学稳定性,环保,低成本的两性吸附剂开辟了新的途径,这些吸附剂具有多种功能,可用于吸附,离子交换,分离,储存和检测存在于非均质介质中的阴离子和阳离子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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