Application of Structured Sol-Gel Nb2O5 Catalyst in Photocatalytic Continuous Process Prototype for Ibuprofen Degradation

被引:2
|
作者
Fidelis, Michel Zampieri [1 ,3 ]
Abreu, Eduardo [1 ]
Andreo, Onelia Aparecida Bassoli [1 ]
Soares, Olivia Salome Goncalves Pinto [2 ,3 ]
Janzen, Frederic Conrad [4 ]
Lenzi, Giane Goncalves [5 ]
机构
[1] Univ Estadual Maringa, Dept Chem Engn, Colombo Ave 5790, BR-87020900 Maringa, Brazil
[2] Univ Porto, Fac Engn, Lab Separat & React Engn Lab Catalysis & Mat LSRE, Rua Dr Roberto Frias, P-4200465 Porto, Portugal
[3] Univ Porto, Fac Engn, ALiCE Associate Lab Chem Engn, Rua Dr Roberto Frias, P-4200465 Porto, Portugal
[4] Univ Tecnol Fed Parana, Dept Elect Engn, R Doutor Washington Subtil Chueire St 330, BR-84017220 Ponta Grossa, PR, Brazil
[5] Univ Tecnol Fed Parana, Dept Chem Engn, R Doutor Washington Subtil Chueire 330, BR-84017220 Ponta Grossa, PR, Brazil
关键词
Emerging pollutants; Continuous Reactor; Niobium Catalysts; Photodegradation; Catalyst reuse; TIO2; FILMS; DYES;
D O I
10.1007/s11244-023-01870-z
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Three distinct sol-gel synthesis methodologies were employed to fabricate niobium catalysts supported on stainless steel meshes via the dip-coating technique, with the objective of their utilization in layered configurations for water purification applications. The structured catalysts were subjected to calcination at three varying temperatures: no calcination, calcination at 823 K, and calcination at 1173 K. Ibuprofen, selected as the model pollutant due to its emerging contaminant profile, was utilized for evaluation. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS) images, in conjunction with adhesion assessments, elucidated that thermally treated catalysts exhibited nearly 80% retention of Nb2O5 nanoparticles adhered uniformly to the support surface. In batch reactor experiments, the catalyst derived from the NbCl5 precursor and polyacrylonitrile (PAN) exhibited the most promising performance, achieving a 90% degradation of the contaminant within a 120 min timeframe. This catalyst, exhibiting superior efficacy, was subsequently employed in tests utilizing photocatalytic bench reactors, where it demonstrated analogous performance to that observed in the batch reactor setup. Upon upscaling to a high-capacity photocatalytic prototype, the degradation efficiency was sustained above that observed in photolytic testing, even after four utilization cycles.
引用
收藏
页码:828 / 842
页数:15
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