State Key Laboratory of Urban Water Resource and Environment (SKLUWRE), Joint Research Center of Biomass Energy Development and Utilization, Harbin Institute of Technology, Harbin 150090, China.
Chongqing Research Institute of HIT, Chongqing 401151, China.
ACS Appl Mater Interfaces. 2024 Jul 10;16(27):34973-34987. doi: 10.1021/acsami.4c05315. Epub 2024 Jun 25.
A peroxymonosulfate oxidation system was developed via modification of β-cyclodextrin (β-CD) on the surface of Fe-doped ZIF-67 (CD/Fe@ZIF-67) as an activator. The 99.7% carbamazepine, 91.3% bisphenol A (BPA), and 95.4% diclofenac (DCF) degradation efficiency were achieved within 10 min, 60, and 1 min, respectively. The hydrophobicity of these three pollutants is positively correlated with their adsorption kinetic constants by CD/Fe@ZIF-67 due to the introduction of β-CD. Scavenger experiments and electron spin resonance spectra confirmed that carbamazepine was preferentially oxidized by SO [λ(SO)(70.5%) > λ(OH)(28.2%) > λ(O)(1.3%)], where SO and O played dominant roles in the degradation of BPA [λ(SO)(71.7%) > λ(O)(22.8%) > λ(OH)(5.5%)], and O was responsible for DCF removal [λ(O) = 93.2%]. Additionally, the particulate catalyst was immobilized in the shell side of a ceramic membrane in a membrane reactor for catalyst recovery. This reactor achieved nearly 100% removal efficiency under optimal conditions: 0.036 wt % catalyst loading, 0.5 mM peroxymonosulfate concentration, 1 L inflow, 10 mg/L initial carbamazepine concentration, and 0.012 L/min hydraulic retention time. In summary, this study elucidates the active role of β-CD in a polymetallic/peroxymonosulfate system and provides valuable insights into the development of effective oxidation methods for pharmaceutical and personal care products in wastewater.
开发了一种过一硫酸盐氧化体系,通过β-环糊精(β-CD)在 Fe 掺杂 ZIF-67(CD/Fe@ZIF-67)表面的修饰作为活化剂。在 10 分钟内实现了 99.7%的卡马西平、91.3%的双酚 A(BPA)和 95.4%的二氯芬酸(DCF)的降解效率。由于引入了β-CD,这三种污染物的疏水性与其被 CD/Fe@ZIF-67 吸附的动力学常数呈正相关。猝灭实验和电子顺磁共振谱证实,卡马西平优先被 SO[λ(SO)(70.5%)>λ(OH)(28.2%)>λ(O)(1.3%)]氧化,其中 SO 和 O 在 BPA 的降解中起主导作用[λ(SO)(71.7%)>λ(O)(22.8%)>λ(OH)(5.5%)],而 O 则负责 DCF 的去除[λ(O) = 93.2%]。此外,将颗粒状催化剂固定在陶瓷膜的壳侧,在膜反应器中进行催化剂回收。在最佳条件下,该反应器实现了近 100%的去除效率:催化剂负载量为 0.036wt%,过一硫酸盐浓度为 0.5mM,进水流量为 1L,初始卡马西平浓度为 10mg/L,水力停留时间为 0.012L/min。总之,本研究阐明了β-CD 在多金属/过一硫酸盐体系中的活性作用,并为开发废水中药品和个人护理产品的有效氧化方法提供了有价值的见解。