The efficiency of UV/H(2)O(2) treatment using KrCl (222 nm) and XeBr (282 nm) excilamps was examined for removal of 2-chlorophenol (2-CP) and 4-chlorophenol (4-CP) from aqueous solution in the molecular form (pH 2 and un-adjusted pH) and anionic form (at pH 11). UV/H(2)O(2) treatment of 2- or 4-CP was initially carried out at un-adjusted pH with varying molar ratios of chlorophenol and H(2)O(2). The para-chlorobenzoic acid was used as a hydroxyl radical (•OH) probe compound. UV/H(2)O(2) treatment of 2- and 4-CP with a molar ratio of 1:25 at ambient pH and a fluence of 4.1 J/cm(2) provided a significant decrease in chemical oxygen demand (COD). Under these conditions, the •OH exposure was found to increase from 0.5 × 10(-11) and 0.4 × 10(-11) to 1.8 × 10(-11) and 1.3 × 10(-11) M min for KrCl and XeBr excilamp, respectively. Compared with direct UV photolysis, the pseudo-first-order fluence-based rate constants of 2- and 4-CP degradation in UV/H(2)O(2) process at a molar ratio of 1:25 were significantly higher for molecular 2-CP and 4-CP in the anionic form using both excilamps. Detailed information on UV fluence and/or the exposure to •OH radicals is proposed to accurately compare studies reporting the effectiveness of AOPs based on excilamps.
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http://dx.doi.org/10.1080/10934529.2012.695953 | DOI Listing |
Nat Commun
January 2025
Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL, USA.
Water is a critical component in polyelectrolyte anion exchange membranes (AEMs). It plays a central role in ion transport in electrochemical systems. Gaining a better understanding of molecular transport and conductivity in AEMs has been challenged by the lack of a general methodology capable of capturing and connecting water dynamics, water structure, and ionic transport over time and length scales ranging from those associated with individual bond vibrations and molecular reorientations to those pertaining to macroscopic AEM performance.
View Article and Find Full Text PDFBiopolymers
March 2025
Guangxi Key Laboratory of Natural Polymer Chemistry and Physics, College of Chemistry and Materials, Nanning Normal University, Nanning, People's Republic of China.
The crosslinked porous corn starch was prepared by two steps: the native corn starch was hydrolyzed by α-amylase and glucoamylase, then the porous corn was crosslinked by sodium trimetaphosphate (STMP). The morphology and size of granules, spherulites, crystal type, molecular structure, swelling properties, thermal stability and adsorption properties of the crosslinked porous starch were investigated. The results indicated that a lot of holes formed in the porous starch, and the particle size of starch granules decreased.
View Article and Find Full Text PDFSmall Methods
January 2025
School of Physical Science and Technology, Center for Energy Conversion Materials & Physics (CECMP), Jiangsu Key Laboratory of Thin Films, Soochow University, Suzhou, 215006, China.
Aqueous zinc-ion battery has low cost, and environmental friendliness, emerging as a promising candidate for next-generation battery systems. However, it still suffers from a limited cycling life, caused by dendritic Zn growth and severe side reactions. Recent research highlights that the Zn (002) crystal plane exhibits superior anti-corrosive properties and a horizontal growth pattern.
View Article and Find Full Text PDFMacromol Rapid Commun
January 2025
Chimie ParisTech, CNRS, Institut de Recherche de Chimie Paris, PSL University, Paris, 75005, France.
The development of catalysts that are both robust and highly active at room temperature can often be seen as a major challenge in anionic polymerization. However, these properties are desirable for polymer synthesis because they allow for easy and sustainable production of interesting materials. Here, iron and magnesium complexes are used to form in situ generated metalate complexes that are shown to be highly active in the room temperature copolymerization of methyl methacrylate and lactide.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
University of Regensburg, Faculty of Chemistry and Pharmacy, Institute of Inorganic Chemistry, Universitätsstraße 31, D-93053, Regensburg, GERMANY.
Aminophosphates are the focus of research on prebiotic phosphorylation chemistry. Their bifunctional nature also makes them a powerful class of organocatalysts. However, the structural chemistry and dynamics of proton-binding in phosphorylation and organocatalytic mechanisms are still not fully understood.
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