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    Wyświetlanie 1-5 z 5
    Tytuł:
    Noble metal modified TiO2 for photocatalytic air purification
    Autorzy:
    Klein, M.
    Grabowska, E.
    Zaleska, A.
    Powiązania:
    https://bibliotekanauki.pl/articles/109916.pdf
    Data publikacji:
    2015
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    photocatalysis
    noble modified TiO2
    air treatment
    toluene
    Opis:
    TiO2 was surface modified with silver, gold, palladium and platinum ion clusters to improve its photocatalytic activity. The effect of metal content and kind of dopant used during preparation procedure on the photoactivity were investigated. in toluene removal which was used as a model volatile organic compound. Toluene, at the concentration of about 100 ppm, was irradiated over noble metal modified TiO2 using light-emitting diodes (LEDs) in four subsequent cycles.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2015, 51, 1; 49-57
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Degradation of toluene using UV/hydrogen peroxide process
    Autorzy:
    Cai, Shaokang
    Sun, Yue
    Gao, Canzhu
    Li, Pengfei
    Cheng, Zhongfa
    Powiązania:
    https://bibliotekanauki.pl/articles/2032937.pdf
    Data publikacji:
    2021
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    AOP
    toluene
    hydrogen peroxide
    spectrofotometer
    toluen
    nadtlenek wodoru
    spektrofotometria
    Opis:
    Toluene in wastewater is volatile and difficult to degrade, and the longer it stays in the water, the higher is the risk. An advanced oxidation process (AOPs) has been used to degrade toluene rapidly and efficiently in wastewater by using ultraviolet light and hydrogen peroxide. Toluene in solution (initial concentration – 180 mg/dm3) with hydrogen peroxide (H2O2 dose – 2022 mg/dm3) was almost decomposed within 150 min. pH as well as the presence of various ions in waste water did not affect the degradation process. However, under strongly acidic conditions (pH less than 3), the chloride ions reduced the degradation efficiency of toluene. Based on the UV spectrophotometer and GC-MS analyses, the degradation pathways were observed: first, the methyl group was oxidized leading to the generation of benzoic acid, the benzene ring was subsequently opened by the action of hydroxyl radical, followed by the gradual decomposition of the intermediate products into small molecules such as water and carbon dioxide.
    Źródło:
    Environment Protection Engineering; 2021, 47, 1; 5-15
    0324-8828
    Pojawia się w:
    Environment Protection Engineering
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Au-RE-TiO2 nanocomposites. surface characteristics and photoactivity
    Autorzy:
    Krukowska, A.
    Reszczynska, J.
    Zaleska, A.
    Powiązania:
    https://bibliotekanauki.pl/articles/109645.pdf
    Data publikacji:
    2014
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    photocatalysis
    modified TiO2
    rare earth metal
    Au nanoparticles
    toluene degradation
    Opis:
    Photocatalysts based on TiO2 co-doped with rare earth metal (RE) and gold nanoparticles have been prepared using a sol-gel method and followed by gold reduction. Specific surface areas of the modified photocatalysts were calculated by the Brunauer-Emmett-Teller method (BET). Diffuse reflectance spectra of the obtained photocatalysts were recorded with a UV-Vis spectrophotometer (DRS UV-Vis). The influence of the type of rare earth metal on photoactivity of Au-RE-TiO2 nanocomposites in model reaction manifested by toluene photodegradation in a gas phase was investigated. The obtained results showed that photodegradation of toluene in the gas phase is possible over Au-RE-TiO2 irradiated by UV or Vis light. The Au-RE-TiO2 photocatalysts relative to undoped TiO2, did not caused an increase of toluene degradation in the air under visible light. The samples doped with Er3+ or Pr3+ presented the highest activity in solar light among of Au-RE-TiO2. It was observed that both metal dopants affected the surface area of TiO2. The Au-RE-TiO2 photocatalysts relative to undoped TiO2 exhibited the absorption properties under Vis light.
    Źródło:
    Physicochemical Problems of Mineral Processing; 2014, 50, 2; 551-561
    1643-1049
    2084-4735
    Pojawia się w:
    Physicochemical Problems of Mineral Processing
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Activated carbon adsorption behaviour of toluene at various temperatures and relative humidity
    Autorzy:
    Görgülü, Adnan
    Yağli, Hüseyin
    Koç, Yildiz
    Koç, Ali
    Baltacioğlu, Ertuğrul
    Powiązania:
    https://bibliotekanauki.pl/articles/207947.pdf
    Data publikacji:
    2019
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    activated carbon
    toluene
    diffusion
    relative humidity
    temperature
    environmental pollution
    węgiel aktywny
    toluen
    dyfuzja
    wilgotność względna
    temperatura
    zanieczyszczenie środowiska
    Opis:
    Filtration plays a major role in managing the rapid increase of environmental pollution and deterioration of atmospheric air quality. One of the most damaging noxious gases in the atmosphere is toluene, which is a common gas that appears in crude oil and is used in various production processes. The adsorption behaviour of activated carbon was examined in dependence of the concentration, temperature and relative humidity. The results showed that increasing air temperature decreased the time to reach the maximum saturation ratio, which occurred due to the increasing pore diffusion coefficient and pore diffusion rate.
    Źródło:
    Environment Protection Engineering; 2019, 45, 1; 111-126
    0324-8828
    Pojawia się w:
    Environment Protection Engineering
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Catalytic decomposition of toluene over La1-xSr xMnO3/palygorskite synthesized catalysts
    Autorzy:
    Song, L.
    Chen, T.
    Chen, D.
    Chen, Y.
    Xie, J.
    Liu, H.
    Powiązania:
    https://bibliotekanauki.pl/articles/207996.pdf
    Data publikacji:
    2013
    Wydawca:
    Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
    Tematy:
    catalysts
    manganese
    manganese oxide
    toluene
    transmission electron microscopy
    X ray diffraction
    Palygorskite
    katalizatory
    mangan
    tlenek manganu
    toluen
    transmisyjna mikroskopia elektronowa
    dyfrakcja promieniowania rentgenowskiego
    Opis:
    Palygorskite (PG) supported La1-xSrxMnO3 catalysts were fabricated by copreripitation. The catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), specific surface area (SSA) and H2 temperature programmed reduction (H 2-TPR). Catalytic activity for VOCs was examined by using toluene as a model compound. The results show that the surface area as well as mechanical strength of catalysts increase substantially after catalysts loaded in PG. XRD patterns show that after calcination at 700 0C, PG as a support in 9% LaMn03/PG and 9% La0.7Sr0.3MnO3/PG was transformed into amorphous phase and the morphology was not destroyed. It was well established that the main reductive components are factually Mn(III) or Mn(IV) oxides in catalysts based on the results of TPR. It was also found that Mn(IV) increases while Mn(III) reduces responding with the increasing amount of Sr. Toluene conversion rate of as-preparedμ% La1-xSr xMnO3/PG increases with the increasing values of x and μ when x=0-0.3 and μ = 3-9%. Toluene can be converted completely at 285 0C by 9% La0.7Sr0.3MnO3/PG catalyst while no significant change was observed after addition on the doping and loading amount of Sr. During a 100 h stability experiment of 9% La 0.7Sr0.3MnO3/PG catalyst, toluene removal was found to be above 95%.
    Źródło:
    Environment Protection Engineering; 2013, 39, 3; 31-42
    0324-8828
    Pojawia się w:
    Environment Protection Engineering
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-5 z 5

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