Chlorinated cyanurates, prepared by application of hypochlorite to cyanuric acid at different ratios, have been commonly employed for disinfection. Combining UV with chlorinated cyanurates (UV/Cl-cyanurates) can be a novel and effective advanced oxidation process (AOP) because (1) Cl-cyanurates structurally resemble chlorinated amides that feature low reactivity with radicals, and (2) Cl-cyanurates, which bear multiple -Cl, may exhibit high molar absorptivity at 254 nm due to red-shifting absorption. Those chemiphysical properties of Cl-cyanurates may facilitate oxidant photolysis rate and lower radical scavenging rates in an AOP, thereby increasing steady-state concentrations of radicals. In this study, UV spectra measured for Cl-cyanurates highlighted molar absorptivities at 254 nm (∼200 Mcm) much higher than free chlorine or HO, while k determined using competition kinetics suggests low •OH reactivity (<1.95 × 10 Ms) for Cl-cyanurates. Photolysis of Cl-cyanurates forms •Cl (i.e., Cl-N cleavage), and •Cl converts to •OH; formation of •OH during a UV/Cl-cyanurates AOP was evaluated using terephthalate as a probe compound. Experiments systematically investigated the effects of pH, Cl dosage, and cyanuric concentration (three key factors affecting the equilibrium concentrations of chlorinated-cynaurate species) on the efficacy of removing three indicator contaminants by UV/Cl-cyanurates AOP. UV/Cl-cyanurates AOP conducted in phosphate buffers or authentic surface waters highlighted efficiencies up to 170% higher than UV/Cl AOP at neutral pH when the same dosage of oxidants was employed, and the presence of certain levels of background ammonia or chloramines further enhanced its performance. Transformation of cyanuric acid or Cl-cyanurates by reacting with radicals during a UV/Cl-cyanurates AOP treatment was minimum. Toxicity assay indicated that UV/Cl-cyanurates AOP treated water was comparable or less toxicity than UV/HO or UV/Cl AOP treated water, and the initial cost estimate indicates UV/Cl-cyanurates AOP is potentially a cost-effective alternative AOP.
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http://dx.doi.org/10.1016/j.watres.2022.118075 | DOI Listing |
Langmuir
January 2025
Surface Science Laboratory, Graduate School of Engineering, Toyota Technological Institute, 2-12-1, Hisakata, Tempaku, Nagoya, Aichi 468-8511, Japan.
Hydrogen-substituted graphdiyne (HsGDY) is a two-dimensional material with an sp-sp carbon skeleton featuring a band gap and a porous structure that enhances ion diffusion. In previous reports, HsGDY growth was limited to metal substrates such as Cu, which then required transfer. Here, we developed a sandwich method that allows HsGDY to be grown directly on the target substrate.
View Article and Find Full Text PDFZhongguo Xiu Fu Chong Jian Wai Ke Za Zhi
January 2025
Key Laboratory for Biomechanics and Mechanobiology of Ministry of Education, School of Biological Science and Medical Engineering, Beijing Advanced Innovation Center for Biomedical Engineering, Beihang University, Beijing, 100083, P. R. China.
Objective: To summarize the latest research progress of graphene and its derivatives (GDs) in bone repair.
Methods: The relevant research literature at home and abroad in recent years was extensively accessed. The properties of GDs in bone repair materials, including mechanical properties, electrical conductivity, and antibacterial properties, were systematically summarized, and the unique advantages of GDs in material preparation, functionalization, and application, as well as the contributions and challenges to bone tissue engineering, were discussed.
ACS Appl Mater Interfaces
January 2025
Henan Provincial Key Laboratory of Nanocomposites and Applications, Institute of Nanostructured Functional Materials, Huanghe Science and Technology College, Zhengzhou, Henan 450006, China.
Due to the high configuration entropy, unique atomic arrangement, and electronic structures, high-entropy materials are being actively pursued as bifunctional catalysts for both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in rechargeable zinc-air batteries (ZABs). However, a relevant strategy to enhance the catalytic activity of high-entropy materials is still lacking. Herein, a hole doping strategy has been employed to enable the high-entropy perovskite La(CrMnFeCoNi)O to effectively catalyze the ORR and OER.
View Article and Find Full Text PDFEnviron Res
January 2025
Ministry of Ecology and Environment South China Institute of Environmental Sciences, Guangzhou 510655, China; Key Laboratory of Water Environmental Simulation and Pollution Control, Ministry of Ecology and Environment, Guangzhou 510655, China. Electronic address:
Iron-activated peroxyacetic acid (PAA) represents an innovative advanced oxidation process (AOP). However, the efficiency of PAA activation by Fe(III) is often underestimated due to the widespread assumption that Fe(III) exhibits much lower ability than Fe(II) to activate PAA. Herein, the oxidative degradation of Rhodamine B (RhB) by Fe(III)-activated PAA process was investigated, and some new insights into the performance and mechanism of the Fe(III)/PAA system were presented.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
College of Chemistry, Beijing University of Chemical Technology, Beijing 100029, People's Republic of China. Electronic address:
The advancement of active packaging for food conservation has attracted considerable interest over time. In the present study, we aims to create and examine active films composed of chitosan (CS), poly(vinyl alcohol) (PVA), and syzygium guineense plant extract (SYZ) for potential use in food preservation. We examined the impact of ethanol extracts from the SYZ plant on the films' tensile strength, physical, antibacterial, and anti-oxidant properties.
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