Carbonate anion photolyzed by solar radiation or combined with peracetic acid to form reactive species for dye degradation

Author(s):  
Ana Paula Nogueira das Neves ◽  
Thayrine Dias Carlos ◽  
Leydiane Barbosa Bezerra ◽  
Whisley Durães Alceno ◽  
Renato Almeida Sarmentob ◽  
...  
2017 ◽  
Vol 51 (24) ◽  
pp. 14217-14224 ◽  
Author(s):  
Meiquan Cai ◽  
Peizhe Sun ◽  
Liqiu Zhang ◽  
Ching-Hua Huang

Author(s):  
Shixiang Wang ◽  
Zhuo Chen ◽  
Zhenran Wang ◽  
Yongsheng Fu ◽  
Yiqing Liu

UV/Fe2+/peracetic acid (PAA) as an efficient and novel advanced oxidation system was reported to produce reactive species (i.e., hydroxyl radicals (˙OH) and organic radicals) for triclosan (TCS) degradation.


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.


Nanomaterials ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1678
Author(s):  
Linh Nguyen ◽  
Pradeep Lamichhane ◽  
Eun Choi ◽  
Geon Lee

Polyethylene glycol-functionalized gold nanoparticles (Au@PEG NPs) were prepared by a simple plasma-assisted method without additional reducing chemicals. After irradiating tetrachloroauric acid (HAuCl4) and polyethylene glycol (PEG) in aqueous medium with an argon plasma jet, the gold precursor transformed into an Au@PEG NP colloid that exhibited surface plasma resonance at 530 nm. When the plasma jet entered the water, additional reactive species were induced through interactions between plasma-generated reactive species and aqueous media. Interaction of the gold precursor with the plasma-activated medium allowed the synthesis of gold nanoparticles (AuNPs) without reductants. The plasma-synthesized Au@PEG NPs had a quasi-spherical shape with an average particle diameter of 32.5 nm. The addition of PEG not only helped to stabilize the AuNPs but also increased the number of AuNPs. Au@PEG NP-loaded paper (AuNP-paper) was able to detect the degradation of rhodamine B, therefore, indicating that AuNP-paper can act as a surface-enhanced Raman scattering platform. Dye degradation by plasma treatment was investigated by optical absorption and Raman spectroscopy. The method proposed for the fabrication of Au@PEG NPs is rapid, low-cost, and environment-friendly and will facilitate the application of plasma-synthesized nanomaterials in sensors.


Space Weather ◽  
2006 ◽  
Vol 4 (6) ◽  
pp. n/a-n/a ◽  
Author(s):  
Tracy Staedter
Keyword(s):  

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