Synthesis, characterization of nanosized ZnCr2O4 and its photocatalytic performance in the degradation of humic acid from drinking water
Закрыть
Articolul precedent
Articolul urmator
546 0
SM ISO690:2012
DUMITRU, Raluca, MANEA, Florica, PĂCURARIU, Cornelia, LUPA, Lavinia, POP, Aniela, CIOABLĂ, Adrian. Synthesis, characterization of nanosized ZnCr2O4 and its photocatalytic performance in the degradation of humic acid from drinking water. In: Central and Eastern European Conference on Thermal Analysis and Calorimetry, Ed. 4, 28-31 august 2017, Chişinău. Germany: Academica Greifswald, 2017, Editia 4, p. 377. ISBN 978-3-940237-47-7.
EXPORT metadate:
Google Scholar
Crossref
CERIF

DataCite
Dublin Core
Central and Eastern European Conference on Thermal Analysis and Calorimetry
Editia 4, 2017
Conferința "Central and Eastern European Conference"
4, Chişinău, Moldova, 28-31 august 2017

Synthesis, characterization of nanosized ZnCr2O4 and its photocatalytic performance in the degradation of humic acid from drinking water


Pag. 377-377

Dumitru Raluca, Manea Florica, Păcurariu Cornelia, Lupa Lavinia, Pop Aniela, Cioablă Adrian
 
Politehnica University of Timisoara
 
 
Disponibil în IBN: 17 octombrie 2019


Rezumat

Zinc chromite (ZnCr2O4) was obtained by the thermolysis of new Zn(II)-Cr(III) oxalate coordination compound, namely [Cr2Zn(C2O4)4(OH2)6]·4H2O. The synthesized precursor was characterized by chemical analysis, vibrational spectrum and thermal analysis. The zinc chromite obtained after a heating treatment of the precursor at 450ºC/1h were investigated by various methods such as XRD, IR, TEM coupled with SAED measurements. The photocatalytic performance of nanosized zinc chromite was assessed for the degradation and mineralization of humic acid (HA) from drinking water source, envisaging the development of the advanced oxidation process for the drinking water treatment technology. A mineralization efficiency of 58.95% was achieved after 180 minutes of 50 mg L-1 HA photocatalysis using zinc chromite under UV irradiation, in comparison with the photolysis that did not allow HA mineralization.