An efficient gamma radiolytic decomposition of one of the extensively used herbicides in the world quizalofo-p-ethyl (QPE) was explored under different experimental conditions. Aqueous solutions of QPE were irradiated by gamma rays emitted by a Cobalt 60 source. QPE aqueous solutions were irradiated at doses of 0.5-3 kGy with 26.31 Gy min dose rate. Obtained results indicated that removal efficiency of 98.5% and 73% of QPE were obtained, respectively, in absence and in presence of dissolved oxygen. Change of absorption spectra, pH effect and Total Organic Carbon (TOC) were carried out and studied. It was found that all absorption bands decreased with increasing irradiation dose and disappear totally after 3 kGy applied dose. Three pH conditions (pH = 10, pH = 6.2 and pH = 3) were applied in radiolytic degradation of QPE showing that the best removal efficiency has been found for neutral pH. Interestingly, the % TOC removal reaches 98% at 3 kGy indicated practically total mineralization. Furthermore, spectrophotometric analyses argued in favour of a pseudo-first-order kinetic of QPE degradation. The resulting apparent rate constant value is approximately = (0.012 ± 0.001) min. Finally, several by-products such as 6-chloroquinoxalin -2-ol, 2-(4-hydroxy-phenyoxy) propionate, 1,4-hydroquinone, quinone, 4-chlorobenzene-1,2diol and 1,2,4-benzenetriol were identified by gas chromatography-mass spectrometry (GC/MS) evidencing that radiation process starting with the fragmentation of the molecule involving the hydroxyl radical, which is generated by the radiolysis of water. Based on the identification intermediates, a degradation mechanistic schema of QPE has been proposed.
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http://dx.doi.org/10.1080/09593330.2021.1944325 | DOI Listing |
Langmuir
January 2025
Institute of Chemical Technology and Engineering, Faculty of Chemical Technology, Poznan University of Technology, ul. Berdychowo 4, PL 60-965 Poznan, Poland.
Despite extensive research on the use of salts to enhance micellar growth, numerous questions remain regarding the impact of ionic exchange and molecular structure on charge neutralization. This study looks into how certain cations (Na, Ca, and Mg) affect the structure of a cocamidopropyl betaine CAPB and sodium dodecylbenzenesulfonate SDBS surfactant mixture, aiming toward applications in targeted delivery systems. The mixture consists of a zwitterionic surfactant, cocamidopropyl betaine (CAPB), and an anionic surfactant, sodium dodecylbenzenesulfonate (SDBS), combined in varying molar ratios at a total concentration of 200 mM.
View Article and Find Full Text PDFInorg Chem
January 2025
Faculty of Chemistry and Chemical Technology, University of Ljubljana, Večna pot 113, 1000 Ljubljana, Slovenia.
Hydrogen-bonded cocrystals have attracted considerable attention as they allow fine-tuning of properties through the choice of hydrogen-bond donors and acceptors. In this study, triphenylarsine oxide (PhAsO) is introduced as a strong hydrogen-bond acceptor molecule. Due to its higher Lewis basicity compared to triphenylphosphine oxide (PhPO), it acts as a strong hydrogen-bond acceptor, which is demonstrated in six new cocrystals with HO and -di(hydroperoxy)cycloalkanes.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8510, Japan.
The visible-light-driven O evolution on oxychloride photocatalysts, such as BiNbOCl, was significantly enhanced by stirring in an aqueous solution containing IrCl in the dark. Various characterizations indicated that highly dispersed IrOHCl-like species spontaneously formed on the oxychloride surface, serving as effective and stable cocatalysts for enhancing O evolution.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Chemistry and Chemical Engineering, State Key Laboratory of Metal Matrix Composites, Frontiers Science Center for Transformative Molecules, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Hydrogel-based sensors typically demonstrate conspicuous swelling behavior in aqueous environments, which can severely compromise the mechanical integrity and distort sensing signals, thereby considerably constraining their widespread applicability. Drawing inspiration from the multilevel heterogeneous structures in biological tissues, an antiswelling hydrogel sensor endowed with high strength, rapid self-recovery, and low swelling ratio was fabricated through a water-induced phase separation and coordination cross-linking strategy. A dense heterogeneous architecture was developed by the integration of "rigid" quadridentate carboxyl-Zr coordination bonds and "soft" hydrophobic unit-rich regions featuring π-π stacking and cation-π interactions into the hydrogels.
View Article and Find Full Text PDFAnal Chem
January 2025
Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, Pennsylvania 15260, United States.
The nuclear pore complex (NPC) is the proteinous nanopore that solely regulates molecular transport between the nucleus and cytoplasm of a eukaryotic cell. Hypothetically, the NPC utilizes the hydrophobic barriers based on the repeats of phenylalanine-glycine (FG) units to selectively and efficiently transport macromolecules. Herein, we quantitatively assess the hydrophobicity of transport barriers confined in the nanopore by applying scanning electrochemical microscopy (SECM).
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