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Visible Light Degradation of Naproxen by Enhanced Photocatalytic Activity of NiO and NiS, Scavenger Study and Focus on Catalyst Support and Magnetization
Author(s) -
Torki Firoozeh,
Faghihian Hossein
Publication year - 2018
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/php.12906
Subject(s) - photocatalysis , catalysis , non blocking i/o , degradation (telecommunications) , materials science , magnetization , chemical engineering , visible spectrum , naproxen , chemistry , magnetic field , organic chemistry , medicine , telecommunications , physics , alternative medicine , engineering , optoelectronics , pathology , quantum mechanics , computer science
This research was aimed to prepare a magnetically photocatalyst enabling to degrade pharmaceutical wastewater and detoxification of pollutant such as naproxen, by visible light irradiation. The nano‐sized NiS and NiO photocatalysts exhibit higher reactivity than their microsized counterparts, but separation of the used photocatalyst from the degradation solution is hard and imperfect. To remove this difficulty, magnetic polypyrrole core‐shell (Fe 3 O 4 @PPY) was synthesized and employed as catalyst support. The magnetization property of the synthesized photocatalysts measured by VSM technique indicated that the photocatalysts were sufficiently magnetized to be readily separated from degradation solution by use of external magnetic field. The DRS study showed that the band gap of the photocatalysts shifted to lower energy after immobilization on the support materials leading to higher degradation efficiency. The optimal efficiency was obtained with the catalysts loaded with 50% of NiO and 50% of NiS. The augmenting effect of H 2 O 2 and the inhibition influence of some organic and inorganic compounds on the degradation process were studied. Regeneration of the used photocatalyst was performed by heat treatment, and the catalyst treated at 400°C retained most of its initial capacity. The degradation capacity was kinetically fast, and the equilibrium was attained within 30 min.