A Thorough Investigation of Photo-catalytic Degradation of ortho and para-Nitro Phenols in binary mixtures: New Insights into Evaluating Degradations Progress Using Chemometrics Approaches

In this study, photocatalytic degradations of 2-nitrophenol and 4-nitrophenol were carried out efficiently using ZnO nanoparticles photo-catalyst under simulated solar irradiation. The photo-decomposition processes were optimized simultaneously by employing central...

Hydrated-electron-based short chain perfluorosulfonic acid decomposition in VUV/sulfite system

Perfluorosulfonic acids (PFSAs) have attracted increasing attention due to their global distribution, high chemical stability and persistence. As a powerful reductant, hydrated electron () shows extraordinary reactivity towards halogenated organic substances like PFSAs. In this study, -based photo-decomposition of perfluorohexane sulfonate (PFHxS) in a VUV/sulfite system was investigated. The kobs of PFHxS decomposition in the studied system was 0.0049 ± 0.0005 min−1, which was 24.5-fold faster than that in a sole VUV system. It was demonstrated that was the main reactive species responsible for PFHxS decomposition. PFHxS decomposition kinetics were accelerated at higher initial solution pH and sulfite dosage, but were restrained when higher initial PFHxS concentration was introduced. Co-existence of chloride showed slight enhancement of PFHxS decomposition, whereas nitrate and bicarbonate suppressed PFHxS decomposition. Accompanying PFHxS decomposition, short chain perfluorocarboxylic acids (PFCAs) were detected as main intermediate products. PFHxS decomposition started with C-S bond fracture, followed by perfluoroalkyl radical hydrolysis reactions and perfluorohexanoic acid (PFHxA) formation. Afterwards, PFHxA was defluorinated by stepwise loss of CF2 units to generate other short chain PFCAs.

Fabrication and Characterization of a Novel Composite Magnetic Photocatalyst β-Bi2O3/BiVO4/MnxZn1−xFe2O4 for Rhodamine B Degradation under Visible Light

β-Bi2O3/BiVO4/MnxZn1−xFe2O4 (BV/MZF) composite magnetic photocatalyst was first synthesized using the hydrothermal and calcination method. BV/MZF was a mesoporous material with most probable pore size and specific surface area of 18 nm and 17.84 m2/g, respectively. Due to its high saturation magnetization (2.67 emu/g), the BV/MZF composite can be easily separated and recovered from solution under an external magnetic field. The results of photo-decomposition experiments show that the decomposition rate of Rhodamine B (RhB) by BV/MZF can reach 92.6% in 3 h under visible light. After three cycles, BV/MZF can still maintain structural stability and excellent pollutant degradation effect. In addition, analysis of the photocatalytic mechanism of BV/MZF for RhB shows that the p-n heterojunction formed in BV/MZF plays a vital role in its photocatalytic performance. This work has potential application in the future for solving environmental pollution.

The elusive dynamics of aqueous permanganate photochemistry

Despite decades of investigation, mechanistic details of aqueous permanganate photo-decomposition remain unclear.

Visible light triggered photo-decomposition of vinyl azides to (E)-stilbene derivatives via 1,2-acyl migration

Photo-decomposition of vinyl azides into corresponding (E)-stilbenes via neighboring amino group assisted ring opening of 2H-azirines, 1,2-acyl migration and enolization.