催化作用
双酚A
双金属片
介孔材料
双金属
化学工程
钴
化学
氧化物
热处理
材料科学
降级(电信)
无机化学
有机化学
物理化学
计算机科学
环氧树脂
工程类
复合材料
电信
作者
Shengjiong Yang,Xiaojie Qiu,Pengkang Jin,Mawuli Dzakpasu,Xiaochang C. Wang,Qionghua Zhang,Lu Zhang,Lei Yang,Dahu Ding,Wendong Wang,Kun Wu
标识
DOI:10.1016/j.cej.2018.07.105
摘要
Porous magnetic cobalt ferrite nanocrystals (CoFe2O4 NC) are synthesized via a one-step process by using bimetal-organic frameworks (Co/Fe bi-MOFs) as a template for the catalytic degradation of bisphenol A (BPA). The properties of the prepared catalyst are evidenced by a series of characterization techniques. Overall, the unique ferromagnetic nature (34.73 emu/g) make its efficient separation from the liquid phase possible. CoFe2O4 NC activates peroxymonosulfate (PMS) to degrade BPA more efficiently than hydrothermally fabricated CoFe2O4 nanoparticles. The difference in catalytic capacity is attributable to the larger specific surface area (60.4 m2 g−1) and well developed mesoporous structure (0.64 cm3 g−1) of the CoFe2O4 NC. EPR analysis demonstrate the production of HO and SO4− radicals in the CoFe2O4 NC/PMS system. The degradation process positively correlates with the increase of initial solution pH, catalysts dosage, and PMS dosage. The degradation rate of 0.112 min−1 is achieved at [PMS]/[BPA] of 10, catalyst dosage of 0.1 g L−1, temperature of 25 °C, and initial pH of 10.2 in deionized water. The existence of Cl- and HCO3−/CO32− show significant positive synergistic effects on the catalytic process. Moreover, simple thermal treatment at 400 °C for 15 min in open air fully regenerates the catalytic capacity of CoFe2O4 NC for reuse. Findings from this work shed light on the rational design of bimetallic oxide catalysts and provide new insight into the development of high-performance magnetic separable catalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI