Rapid photocatalytic degradation of phenol from water using composite nanofibers under UV; Environmental Sciences Europe; Vol. 32, iss. 1

Bibliografiske detaljer
Parent link:Environmental Sciences Europe
Vol. 32, iss. 1.— 2020.— [160, 8 p.]
Institution som forfatter: Национальный исследовательский Томский политехнический университет Инженерная школа природных ресурсов Отделение геологии
Andre forfattere: Mohamed A. Alaa, Yousef S. Samy, Nasser W. S. Walaa, Osman T. A. S. Tarek Abdel Sadek, Knebel A. Alexander, Sanchez E. P. V. Elvia P. Valadez, Mokhamed Takhid Khashim (Hashem) Abdelrazek
Summary:Title screen
The removal of phenol from aqueous solution via photocatalytic degradation has been recognized as an environmentally friendly technique for generating clean water. The composite nanofibers containing PAN polymer, CNT, and TiO2 NPs were successfully prepared via electrospinning method. The prepared photocatalyst is characterized by SEM, XRD, and Raman spectroscopy. Different parameters are studied such as catalyst amount, the effect of pH, phenol concentration, photodegradation mechanism, flow rate, and stability of the composite nanofiber to evaluate the highest efficiency of the photocatalyst.
Sprog:engelsk
Udgivet: 2020
Fag:
Online adgang:https://doi.org/10.1186/s12302-020-00436-0
Format: Electronisk Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=663672
Beskrivelse
Summary:Title screen
The removal of phenol from aqueous solution via photocatalytic degradation has been recognized as an environmentally friendly technique for generating clean water. The composite nanofibers containing PAN polymer, CNT, and TiO2 NPs were successfully prepared via electrospinning method. The prepared photocatalyst is characterized by SEM, XRD, and Raman spectroscopy. Different parameters are studied such as catalyst amount, the effect of pH, phenol concentration, photodegradation mechanism, flow rate, and stability of the composite nanofiber to evaluate the highest efficiency of the photocatalyst.
DOI:10.1186/s12302-020-00436-0