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Enhanced adsorption capacity and selectivity towards strontium ions in aqueous systems by sulfonation of CO2 derived porous carbon

机译:通过磺化CO 2 衍生的多孔碳增强水系统中锶离子的吸附能力和选择性

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Oxygen-enriched carbon materials derived from carbon dioxide were functionalized using sulfonic acid to remove Sr2+ ions from aqueous solutions. Synthesized sulfonated porous carbon materials (PC-SO3H) showed higher adsorption capacity and selectivity towards Sr2+ than non-functionalized porous carbons (PC). The formation of the C-SO3H functional group in PC-SO3H and its ability to proton exchange with Sr2+ was the main contributor to the enhanced performance. The maximum uptake capacity of Sr2+ by PC-SO3H was 18.97 mg g?1, which was 1.74 times greater than PC. PC-SO3H removed 99.9% and 97.6% of Sr2+ from aqueous solutions with initial Sr2+ concentrations of 5 mg L?1 and 10 mg L?1, respectively. Sr2+ adsorption showed rapid kinetics, reaching the adsorption equilibrium within 1 h with high adsorption capacity at equilibrium which is 3.52 times greater than that of PC. Additionally, PC-SO3H selectively adsorbed Sr2+ even in the presence of excess amounts of competing ions. Sulfonation of oxygen-enriched carbon had a significant effect on enhancing the affinity towards Sr2+ and suppressing adsorption towards other competing ions.
机译:使用磺酸对源自二氧化碳的富氧碳材料进行功能化,以从水溶液中去除Sr 2 + 离子。合成的磺化多孔碳材料(PC-SO 3 H)显示出更高的吸附能力和对Sr 2 + 的选择性比未官能化的多孔碳(PC) PC-SO 3 H中C-SO 3 H官能团的形成及其质子交换能力与Sr 2 + 的交换是增强性能的主要原因。 PC-SO 3 H对Sr 2 + 的最大吸收容量为18.97 mg g < sup>?1 ,是PC的1.74倍。 PC-SO 3 H从初始Sr <的水溶液中去除了99.9%和97.6%的Sr 2 + small> 2 + 浓度为5 mg L ?1 和10 mg L ?1 。 Sr 2 + 吸附表现出快速的动力学,在1 h内达到吸附平衡,在平衡状态下的吸附能力高,是PC的3.52倍。此外,即使存在过量竞争离子,PC-SO 3 H仍会选择性吸附Sr 2 + 。富氧碳的磺化对增强对Sr 2 + 的亲和力和抑制对其他竞争离子的吸附具有显著作用。

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