Vše

Co hledáte?

Vše
Projekty
Výsledky výzkumu
Subjekty

Rychlé hledání

  • Projekty podpořené TA ČR
  • Významné projekty
  • Projekty s nejvyšší státní podporou
  • Aktuálně běžící projekty

Chytré vyhledávání

  • Takto najdu konkrétní +slovo
  • Takto z výsledků -slovo zcela vynechám
  • “Takto můžu najít celou frázi”

Degradation of atrazine by ZnxCu1 (-) xFe2O4 nanomaterial-catalyzed sulfite under UV-vis light irradiation: Green strategy to generate SO4 center dot(-)

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F18%3A73583091" target="_blank" >RIV/61989592:15310/18:73583091 - isvavai.cz</a>

  • Výsledek na webu

    <a href="http://www.sciencedirect.com/science/article/pii/S0926337317308263" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0926337317308263</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.apcatb.2017.09.001" target="_blank" >10.1016/j.apcatb.2017.09.001</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Degradation of atrazine by ZnxCu1 (-) xFe2O4 nanomaterial-catalyzed sulfite under UV-vis light irradiation: Green strategy to generate SO4 center dot(-)

  • Popis výsledku v původním jazyce

    Degradation of atrazine, a widely-used herbicide, by a novel advanced oxidation process was investigated through photo-catalyzing sulfite, the precursor of sulfate radical (SO4 center dot(-)) in this study, by zinc-copper ferrites (ZnxCu1 - xFe2O4) under UV-vis light irradiation. The ZnxCu1 - xFe2O4 with different ratios of Zn to Cu was synthesized through a facile sol-gel combustion method, and characterized by X-ray powder diffractometry, scanning electron microscopy, transmission electron microscopy, porosimetry, and UV-vis diffuse reflectance spectroscopy, and by a vibrating sample magnetometer and Mossbauer spectrometer. The Zn0.8Cu0.2Fe2O4 demonstrated the highest photocatalytic ability to activate sulfite for the degradation of atrazine under current experimental conditions. The sulfate radical generated in the UV-vis light/Zn0.8Cu0.2Fe2O4/qulfite system was identified as the main reactive species through radical quenching experiments and measuring two important byproducts (atrazine-desethyl and atrazine-desisopropyl). The XPS spectra of fresh and used catalysts were analyzed to further elucidate the reaction mechanisms. There are two possible approaches to produce SO4 center dot(-): the oxidation of sulfite by photo-generated holes and the accelerated decomposition of metal-sulfito complexes (Fe (III)-sulfito and Cu(II)-sulfito) on the surface of Zn0.8Cu0.2Fe2O4. Based on the detected byproducts, the transformation pathways of atrazine by UV-vis light/Zn0.8Cu0.2Fe2O4/sulfite were proposed as well. After the complete decomposition of atrazine, the used catalysts could be magnetically recovered using a magnet and no sulfite remained in the system. The results suggest that the UV-vis light/Zn0.8Cu0.2Fe2O4/sulfite system is a &quot;green&quot; advanced oxidation technology for future application in wastewater treatment.

  • Název v anglickém jazyce

    Degradation of atrazine by ZnxCu1 (-) xFe2O4 nanomaterial-catalyzed sulfite under UV-vis light irradiation: Green strategy to generate SO4 center dot(-)

  • Popis výsledku anglicky

    Degradation of atrazine, a widely-used herbicide, by a novel advanced oxidation process was investigated through photo-catalyzing sulfite, the precursor of sulfate radical (SO4 center dot(-)) in this study, by zinc-copper ferrites (ZnxCu1 - xFe2O4) under UV-vis light irradiation. The ZnxCu1 - xFe2O4 with different ratios of Zn to Cu was synthesized through a facile sol-gel combustion method, and characterized by X-ray powder diffractometry, scanning electron microscopy, transmission electron microscopy, porosimetry, and UV-vis diffuse reflectance spectroscopy, and by a vibrating sample magnetometer and Mossbauer spectrometer. The Zn0.8Cu0.2Fe2O4 demonstrated the highest photocatalytic ability to activate sulfite for the degradation of atrazine under current experimental conditions. The sulfate radical generated in the UV-vis light/Zn0.8Cu0.2Fe2O4/qulfite system was identified as the main reactive species through radical quenching experiments and measuring two important byproducts (atrazine-desethyl and atrazine-desisopropyl). The XPS spectra of fresh and used catalysts were analyzed to further elucidate the reaction mechanisms. There are two possible approaches to produce SO4 center dot(-): the oxidation of sulfite by photo-generated holes and the accelerated decomposition of metal-sulfito complexes (Fe (III)-sulfito and Cu(II)-sulfito) on the surface of Zn0.8Cu0.2Fe2O4. Based on the detected byproducts, the transformation pathways of atrazine by UV-vis light/Zn0.8Cu0.2Fe2O4/sulfite were proposed as well. After the complete decomposition of atrazine, the used catalysts could be magnetically recovered using a magnet and no sulfite remained in the system. The results suggest that the UV-vis light/Zn0.8Cu0.2Fe2O4/sulfite system is a &quot;green&quot; advanced oxidation technology for future application in wastewater treatment.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10403 - Physical chemistry

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/LO1305" target="_blank" >LO1305: Rozvoj centra pokročilých technologií a materiálů</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2018

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Applied Catalysis B: Environmental

  • ISSN

    0926-3373

  • e-ISSN

  • Svazek periodika

    221

  • Číslo periodika v rámci svazku

    FEB

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    13

  • Strana od-do

    380-392

  • Kód UT WoS článku

    000414109700039

  • EID výsledku v databázi Scopus

    2-s2.0-85029679846