Sathishkumar Panneerselvam, Mangalaraja Ramalinga Viswanathan, Rozas Oscar, Vergara Carola, Mansilla Héctor D, Gracia-Pinilla M A, Anandan Sambandam
Advanced Ceramics and Nanotechnology Laboratory, Department of Materials Engineering, Faculty of Engineering, University of Concepcion, Concepcion 407-0409, Chile; Department of Chemistry, Periyar Maniammai University, Vallam, Thanjavur 613403, Tamil Nadu, India.
Advanced Ceramics and Nanotechnology Laboratory, Department of Materials Engineering, Faculty of Engineering, University of Concepcion, Concepcion 407-0409, Chile.
Chemosphere. 2016 Mar;146:216-25. doi: 10.1016/j.chemosphere.2015.12.011. Epub 2015 Dec 28.
Norflurazon (4-chloro-5-(methylamino)-2-[3-(trifluoromethyl)phenyl]pyridazin-3(2H)-one; C12H9ClF3N3O) is an excellent weed controlling agent being practiced in the agricultural lands. The excessive addition or the undissolved Norflurazon (maximum solubility 28 mg/L at 25 °C) enters into the aquatic environment and causes the adverse effects associated with its high concentration. To avoid the perilous effects, visible light assisted photocatalysis set-up coupled with the 42 kHz ultrasound producing bath type sonicator is used to completely mineralize the Norflurazon. TiO2, ZnO and gold loaded zinc oxide nanocatalysts were utilized to study the mineralization of Norflurazon. Au-ZnO shows the greater efficiency for the sonophotocatalytic removal of Norflurazon among the various nanocatalysts employed to study the mineralization. The order of Norflurazon mineralization was sonophotocatalysis > sonocatalysis > photocatalysis. The additive effect was achieved for the sonophotocatalytic degradation. The high performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometric (LCMS) analyses were employed to identify the various intermediates produced during the mineralization. The identification of four pseudo molecular ions and various intermediates using the LCMS analysis evidently suggests the sonophotocatalytic degradation was preceded in various decay pathways. A suitable mechanism has been proposed for the sonophotocatalytic mineralization of Norflurazon.
氟草敏(4-氯-5-(甲氨基)-2-[3-(三氟甲基)苯基]哒嗪-3(2H)-酮;C12H9ClF3N3O)是一种在农田中广泛使用的优良除草剂。过量添加或未溶解的氟草敏(25℃时最大溶解度为28mg/L)进入水环境并因其高浓度而产生不利影响。为避免这些危险影响,采用可见光辅助光催化装置与产生42kHz超声波的浴式超声处理器相结合,以完全矿化氟草敏。利用TiO2、ZnO和负载金的氧化锌纳米催化剂研究氟草敏的矿化作用。在用于研究矿化作用的各种纳米催化剂中,Au-ZnO对声光催化去除氟草敏显示出更高的效率。氟草敏矿化的顺序为声光催化>声催化>光催化。声光催化降解实现了加和效应。采用高效液相色谱(HPLC)和液相色谱-质谱联用(LCMS)分析来鉴定矿化过程中产生的各种中间体。通过LCMS分析鉴定出四个准分子离子和各种中间体,这显然表明声光催化降解是通过多种衰变途径进行的。已提出了一种适用于氟草敏声光催化矿化的机理。