Degradation of Methyl 2-Aminobenzoate (Methyl Anthranilate) by H2O2/UV: Effect of Inorganic Anions and Derived Radicals

التفاصيل البيبلوغرافية
العنوان: Degradation of Methyl 2-Aminobenzoate (Methyl Anthranilate) by H2O2/UV: Effect of Inorganic Anions and Derived Radicals
المؤلفون: Davide Vione, Debora Fabbri, Mohamed Sarakha, Grazia Maria Lanzafame
المساهمون: Institut de Chimie de Clermont-Ferrand (ICCF), SIGMA Clermont (SIGMA Clermont)-Institut de Chimie du CNRS (INC)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS), Dipartimento di Chimica [Torino], Università degli studi di Torino = University of Turin (UNITO), Università degli studi di Torino (UNITO), Università degli Studi di Torino, Dipartimento di Chimica, Torino, Università degli Studi di Torino, Centro Interdipartimentale NatRisk, Grugliasco
المصدر: Molecules; Volume 22; Issue 4; Pages: 619
Molecules
Molecules, 2017, 22 (4), ⟨10.3390/molecules22040619⟩
Molecules, MDPI, 2017, 22 (4), ⟨10.3390/molecules22040619⟩
بيانات النشر: Multidisciplinary Digital Publishing Institute, 2017.
سنة النشر: 2017
مصطلحات موضوعية: Radical, Pharmaceutical Science, hydrogen peroxide, 02 engineering and technology, 010501 environmental sciences, Photochemistry, 01 natural sciences, Chloride, Analytical Chemistry, chemistry.chemical_compound, Reaction rate constant, advanced oxidation processes, methyl anthranilate, methyl 2-aminobenzoate, photodegradation intermediates, emerging contaminants, Drug Discovery, medicine, [CHIM]Chemical Sciences, Physical and Theoretical Chemistry, Hydrogen peroxide, Photodegradation, 0105 earth and related environmental sciences, Methyl anthranilate, Organic Chemistry, Substrate (chemistry), 021001 nanoscience & nanotechnology, chemistry, 13. Climate action, Chemistry (miscellaneous), Molecular Medicine, Flash photolysis, 0210 nano-technology, medicine.drug, Nuclear chemistry
الوصف: This study shows that methyl 2-aminobenzoate (also known as methyl anthranilate, hereafter MA) undergoes direct photolysis under UVC and UVB irradiation and that its photodegradation is further accelerated in the presence of H2O2. Hydrogen peroxide acts as a source of hydroxyl radicals (·OH) under photochemical conditions and yields MA hydroxyderivatives. The trend of MA photodegradation rate vs. H2O2 concentration reaches a plateau because of the combined effects of H2O2 absorption saturation and ·OH scavenging by H2O2. The addition of chloride ions causes scavenging of ·OH, yielding Cl2·− as the most likely reactive species, and it increases the MA photodegradation rate at high H2O2 concentration values. The reaction between Cl2·− and MA, which has second-order rate constant k C l 2 • − + M A = (4.0 ± 0.3) × 108 M−1·s−1 (determined by laser flash photolysis), appears to be more selective than the ·OH process in the presence of H2O2, because Cl2·− undergoes more limited scavenging by H2O2 compared to ·OH. While the addition of carbonate causes ·OH scavenging to produce CO3·− ( k C O 3 • − + M A = (3.1 ± 0.2) × 108 M−1·s−1), carbonate considerably inhibits the photodegradation of MA. A possible explanation is that the elevated pH values of the carbonate solutions make H2O2 to partially occur as HO2−, which reacts very quickly with either ·OH or CO3·− to produce O2·−. The superoxide anion could reduce partially oxidised MA back to the initial substrate, with consequent inhibition of MA photodegradation. Fast MA photodegradation is also observed in the presence of persulphate/UV, which yields SO4·− that reacts effectively with MA ( k S O 4 • − + M A = (5.6 ± 0.4) × 109 M−1·s−1). Irradiated H2O2 is effective in photodegrading MA, but the resulting MA hydroxyderivatives are predicted to be about as toxic as the parent compound for aquatic organisms (most notably, fish and crustaceans).
وصف الملف: application/pdf
اللغة: English
تدمد: 1420-3049
DOI: 10.3390/molecules22040619
DOI: 10.3390/molecules22040619⟩
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b60b635c56d00e340799d4306ef32cd6
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....b60b635c56d00e340799d4306ef32cd6
قاعدة البيانات: OpenAIRE
الوصف
تدمد:14203049
DOI:10.3390/molecules22040619