Hayat Anwer, Huang Liangai, Wang Zongpeng, Ullah Raza, He Sailing
National Engineering Research Center for Optical Instruments, College of Optical Science and Engineering, Zhejiang University Hangzhou 310058 People's Republic of China
School of Materials Science and Engineering, Zhejiang Sci-Tech University Hangzhou 310018 China.
RSC Adv. 2024 Mar 27;14(15):10229-10243. doi: 10.1039/d4ra00812j. eCollection 2024 Mar 26.
Doping active agents into metal-organic frameworks (MOFs) is widely sought after owing to its potential to enhance adsorption and photocatalytic efficiency, surpassing the potential of bare frameworks. This study incorporated a catalytically active NS-ligand (1,2-benzisothiazolin-3-one) into a very stable and porous PCN-600 MOF an synthesis approach. The NS-ligand, which matched with the host ligands of PCN-600, enabled the highly efficient synthesis of NS-co-doped MOFs. The pristine PCN-600 framework and morphology were retained in the MOF altered with the NS-ligand, as demonstrated by XRD, FTIR, and SEM characterizations. A high electron density was generated due to the synergistic effect between the defects in the NS-co-doped photocatalyst and engineered active sites. This facilitated the adsorption-assisted photocatalytic decontamination of metronidazole with an 87% removal by PCN-600-NS-10 compared to 43% by pristine PCN-600 within a total time of 150 min. The MOF doped with the NS-ligand exhibited a reduced band gap and enhanced adsorption and photocatalytic capabilities compared to pristine PCN-600. The impact of operational parameters, such as catalyst dosage, initial solution pH, and MNZ concentration, was also explored. Pseudo-second and pseudo-first order models were found to describe the adsorption and degradation kinetics of metronidazole and the Dubinin-Radushkevich model was found to fit the equilibrium adsorption results. The thermodynamic characteristics of adsorption processes (Δ, Δ, and Δ) demonstrated that adsorption was physical, spontaneous, and exothermic and resulted in increased entropy.
由于将活性剂掺杂到金属有机框架(MOF)中具有提高吸附和光催化效率的潜力,超过了裸框架的潜力,因此受到广泛关注。本研究采用一种合成方法,将具有催化活性的NS配体(1,2-苯并异噻唑啉-3-酮)掺入非常稳定且多孔的PCN-600 MOF中。与PCN-600的主体配体相匹配的NS配体,实现了NS共掺杂MOF的高效合成。XRD、FTIR和SEM表征表明,用NS配体改性的MOF保留了原始PCN-600的框架和形态。NS共掺杂光催化剂中的缺陷与工程活性位点之间的协同效应产生了高电子密度。这促进了吸附辅助的甲硝唑光催化去污,在150分钟的总时间内,PCN-600-NS-10对甲硝唑的去除率为87%,而原始PCN-600的去除率为43%。与原始PCN-600相比,掺杂NS配体的MOF表现出减小的带隙以及增强的吸附和光催化能力。还探讨了催化剂用量、初始溶液pH值和甲硝唑浓度等操作参数的影响。发现伪二级和伪一级模型可以描述甲硝唑的吸附和降解动力学,并且发现Dubinin-Radushkevich模型适合平衡吸附结果。吸附过程的热力学特征(Δ、Δ和Δ)表明吸附是物理的、自发的和放热的,并且导致熵增加。