Adsorption mechanism of acid orange 7 on photocatalytic materials based on TiO2

MRS Advances ◽  
2019 ◽  
Vol 4 (61-62) ◽  
pp. 3399-3405
Author(s):  
A. Arteaga-Jiménez ◽  
A. I. Caudana-Campos ◽  
A. L. García-García ◽  
E. Hernández-Zapata ◽  
M. A. Vidales-Hurtado

ABSTRACTThe degradation of organic molecules in an aqueous medium using heterogeneous photocatalysis depends on the chemical composition and concentration of the organic compound, the crystalline and morphological nature of the photocatalyst, the pH of the dye dilution, and the reaction temperature. Since photocatalytic degradation is a process that occurs on the surface of the catalytic material, it is desirable to induce maximum adsorption of the organic compound. One strategy to achieve this is to functionalize the surface of the catalyst to retain the molecule of interest. In this work, we studied the interaction of acid orange 7 (AO7) with commercial TiO2-anatase powder catalyst, and with a catalyst synthesized in house using titanium tetrachloride and ethanolamine (TiO2-et). Our results indicate that there is no adsorption of the AO7 dye on the TiO2-et particles. The infrared spectrum of the TiO2-et particles is presented.

2003 ◽  
Vol 47 (5) ◽  
pp. 211-216 ◽  
Author(s):  
J. Li ◽  
P.L. Bishop

Microelectrode measurements were conducted to obtain nitrate, pH and redox potential profiles within anoxic denitrifying biofilms. The influence of a toxic organic compound (acid orange 7) on biofilm microprofiles was also monitored using microelectrodes. The data provide evidence that the denitrifying biofilms were stratified into an anoxic layer and an anaerobic layer. The anaerobic zone might provide a niche for the biodegradation of recalcitrant organic compounds in biofilms. It was found that acid orange 7 and its biodegradation byproducts had only a slight impact on biofilm nitrate, pH and redox potential profiles.


2012 ◽  
Vol 106 (2) ◽  
pp. 297-311 ◽  
Author(s):  
Michal Baudys ◽  
Martin Zlámal ◽  
Josef Krýsa ◽  
Jaromír Jirkovský ◽  
Petr Kluson

1972 ◽  
Vol 45 ◽  
pp. 265-270
Author(s):  
L. M. Shul'man

The probable parent-molecules of radicals such as C3 and N2+ are discussed, and it is concluded that cometary nuclei may contain complicated organic molecules, such as C3H4, CH2N2, and C4H2. It is suggested that these molecules are formed by radiation synthesis in solid phase. In a time interval of order 107 to 109 yr bombardment from cosmic rays would be expected to transform the chemical composition to a depth of 1 m. Solar cosmic rays do not penetrate as far, and as a result the surface layer of the nucleus can be enriched with unsaturated hydrocarbons. After a critical concentration of this explosive material is reached a further burst of solar cosmic rays can initiate an explosion and thus an outburst in the comet's brightness. This mechanism is the only one advanced to date that can explain the synchronism of the energy output over the whole nuclear surface.


2013 ◽  
Vol 67 (11) ◽  
pp. 2560-2567 ◽  
Author(s):  
Fan Yang ◽  
Xiaojie Song ◽  
Lifeng Yan

Cationic paper was prepared by reaction of paper with 2,3-epoxypropyltrimethylammonium chloride in aqueous suspension, and tested as low-cost adsorbent for wastewater treatment. The experimental results revealed that anionic dyes (Acid Orange 7, Acid Red 18, and Acid Blue 92) were adsorbed on the cationic paper nicely. The maximum amount of dye Acid Orange 7 adsorbed on cationic paper was 337.2 mg/g in experimental conditions. The effects of initial dye concentration, temperature, and initial pH of dye solution on adsorption capacity of cationic paper were studied. The pseudo-first-order and pseudo-second-order kinetic models were applied to describe the kinetic data. The Freundlich and Langmuir adsorption models were used to describe adsorption equilibrium. The thermodynamic data indicated that the adsorption process of dye on cationic paper occurred spontaneously.


Author(s):  
Saranyoo Chaiwichian ◽  
Buagun Samran

Abstract Monoclinic BiVO4 photocatalyst films decorated on glass substrates were successfully fabricated via a dip-coating technique with different annealing temperatures of 400 °C, 450 °C, 500°C, and 550 °C. All of the physical and chemical properties of as-prepared BiVO4 photocatalyst film samples were investigated using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV–vis diffuse reflectance spectra techniques. The results revealed that the as-prepared BiVO4 photocatalyst film samples retained a monoclinic phase with an average particle size of about 50 – 100 nm. Moreover, the BiVO4 photocatalyst film samples showed a strong photoabsorption edge in the range of visible light with the band gap energy of 2.46 eV. The photocatalytic activities of all the film samples were tested by the degradation of model acid orange 7 under visible light irradiation. The BiVO4 photocatalyst film sample annealed at a temperature of 500 °C showed the highest photoactivity efficiency compared with other film samples, reaching up to 51%within 180 min. In addition, the stability and reusability of BiVO4 photocatalyst film sample made with an annealing temperature of 500 °C did not show loss of photodegradation efficiency of acid orange 7 after ten recycles. A likely mechanism of the photocatalytic process was established by trapping experiments, indicating that the hydroxyl radical scavenger species can be considered to play a key role for acid orange 7 degradation under visible light irradiation.


2008 ◽  
Vol 138 (1-3) ◽  
pp. 231-238 ◽  
Author(s):  
Hui Zhang ◽  
Yujuan Lv ◽  
Fang Liu ◽  
Daobin Zhang

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