scholarly journals Oxidative degradation of Orange G in aqueous solution by persulfate activated with pyrite

Author(s):  
Xin Zhang ◽  
Yingzhi Qin ◽  
Weiting Zhang ◽  
Yali Zhang ◽  
Guang-En Yuan

Abstract Orange G (OG), a typical azo dye in textile wastewaters, has been the subject of intense investigations. This study investigated oxidative degradation of OG in aqueous solution by persulfate (PS) activated with pyrite. A complete destruction of OG was achieved within 60 min in the pyrite/PS system. Lower solution pH, smaller pyrite particles and higher pyrite dosage was beneficial for OG degradation. Higher PS concentration was also in favour of OG degradation, but excess PS would decrease the removal efficiency of OG. The addition of HCO3− and H2PO4− but Cl− had inhibitory effects on the destruction of OG. The results of quenching experiments and electron paramagnetic resonance tests proved that SO4•− and •OH were the dominant reactive species responsible for OG degradation in the pyrite/PS system. The azo bond, naphthalene ring and benzene ring of OG were all destroyed by the generated reactive species. The mineralization rate of OG reached 34.4% after 60 min of reaction. This work will provide information for understanding azo dye degradation by pyrite activated PS.

2019 ◽  
Vol 9 (9) ◽  
pp. 1958 ◽  
Author(s):  
John Kyriakopoulos ◽  
Eleana Kordouli ◽  
Kyriakos Bourikas ◽  
Christos Kordulis ◽  
Alexis Lycourghiotis

The majority of the photocatalysts studied for azo-dye degradation are based on semiconductor materials. Studies reported on non-semiconducting materials are very scarce. In the present work, we studied the fullerene (C60) ability to accelerate photodegradation of the dye’s azo bond in the presence of ascorbic acid. A series of C60 supported on ordered mesoporous silica (MCM-41) catalysts, containing 1, 3, 6, 9, and 12 wt % of fullerene C60, was studied using Orange G (OG) as representative azo-dye. This study showed that partial decolorization is achieved in the dark by simple adsorption of the dye on the bare surface of the carrier. The extent of decolorization increases with the irradiation of the suspension due to photocatalytic degradation of the azo-bond. This is maximized over the sample containing 3 wt % of C60 and it has been attributed to the best combination of the extent of the dye adsorption with the high intrinsic photocatalytic activity of small C60 clusters predominated in this sample. This catalyst proved to be quite stable upon five subsequent photocatalytic cycles, losing less than 5% of its initial activity. No degradation of OG takes place in the absence of ascorbic acid.


2012 ◽  
Vol 33 (14) ◽  
pp. 1545-1552 ◽  
Author(s):  
Honghai Wu ◽  
Xiaowen Dou ◽  
Dayi Deng ◽  
Yufeng Guan ◽  
Liguo Zhang ◽  
...  

2020 ◽  
Vol 20 (6) ◽  
pp. 3478-3485 ◽  
Author(s):  
Jun Shen ◽  
Zhi-Jun Li ◽  
Ze-Feng Hang ◽  
Su-Fan Xu ◽  
Qin-Qin Liu ◽  
...  

Reactive oxygen species (ROS), as primary intermediates formed during photocatalytic reactions, are critical for a photocatalyst to realize high activity. The major objective of this study was to investigate the regulation of ROS involved in the photocatalytic degradation process via constructing a typical metal-semiconductor hybrid heterojunction using Ag nanoparticles/anatase TiO2 as an example. Based on radical capturing, electron paramagnetic resonance, and electron spin resonance experiments, an increase in the available ROS can be achieved in the Ag/TiO2 heterojunction due to the fast separation of photogenerated carriers. In addition, due to the change in the electron transfer pathway, superoxide radicals (·O−2) are the dominant reactive species responsible for dye degradation using Ag/TiO2 rather than hydroxyl radicals (·OH) as the main free radicals in pristine TiO2. This study offers fresh insight into the regulation of ROS in photodegradation via the construction of a Ag/TiO2 heterojunction.


1981 ◽  
Vol 59 (22) ◽  
pp. 3212-3217 ◽  
Author(s):  
J. William Lown ◽  
Hsiao-Hsiung Chen

The antitumor antibiotic daunorubicin, upon reduction in aqueous solution, gives a transient resolved epr spectrum of linewidth 17.0 G and g value of 2.0024. This is ascribed to the semiquinone previously tentatively assigned in the unresolved epr spectrum obtained by microsomal activation of the antibiotic. By reference to the epr spectrum of quinizarin semiquinone in aqueous solution the individual proton hyperfine splitting constants in both spectra were tentatively assigned by computer simulation. LCAO–MO calculations of one-electron wave function spin densities in both species gave good agreement between calculated and observed hfs for values of the parameters βCO/βCC = 1.8, δα = 1.4, allowing definite assignment of the aromatic protons. By considering the angular dependence of the ring A benzylic proton hfs it was possible to discriminate between two alternative half-chair conformations of daunorubicin semiquinone. The preferred conformation of the intermediate is tentatively assigned as that which places both 7 and 9 oxygen functions equatorial and the C-9 acetyl group axial.


2017 ◽  
Vol 19 (48) ◽  
pp. 32580-32588 ◽  
Author(s):  
Wen-Lan Wang ◽  
Yuan Min ◽  
Sheng-Song Yu ◽  
Wei Chen ◽  
Jie-Jie Chen ◽  
...  

Proton-coupled electron transfer mechanisms of riboflavin bound hemin in aqueous solution are elucidated by spectroelectrochemical analysis, the electron paramagnetic resonance method and theoretical calculations.


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