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设计一种新型的海泥/钛酸盐光催化剂,在超声/紫外线/过氧化氢存在下,从水介质中去除头孢氨苄抗生素:降解途径和机制。

Design a new photocatalyst of sea sediment/titanate to remove cephalexin antibiotic from aqueous media in the presence of sonication/ultraviolet/hydrogen peroxide: Pathway and mechanism for degradation.

机构信息

Department of Environment, Bushehr Branch, Islamic Azad University, Bushehr, Iran.

Department of Environment, Bushehr Branch, Islamic Azad University, Bushehr, Iran.

出版信息

Ultrason Sonochem. 2020 Jul;65:105062. doi: 10.1016/j.ultsonch.2020.105062. Epub 2020 Mar 9.

Abstract

The aim of the current study was directed to develop a new sea sediment/titanate photocatalyst to remove cephalexin from aqueous media in the presence of ultraviolet (UV) light, hydrogen peroxide (HO), and ultrasonic waves. The influence of furnace temperature (300, 350, 400, and 500 °C), furnace residence time (1, 2, 3, and 4 h), and ratio of sea sediment: titanium (0-6 v: w) on the physicochemical properties and the cephalexin removal by the sea sediment/titanate photocatalyst was explored. The technique of FTIR, SEM/EDX, XRD, BET, BJH, and Mapping was used to determine the physicochemical properties of the generated photocatalyst. The maximum cephalexin removal (94.71%) was obtained at the furnace temperature of 500 °C, the furnace residence time of 2 h, and the sea sediment: titanium ratio of 1:6 (=12 mL TiO/2 g sea sediment). According to the acquired results, the surface area of the optimized catalyst, namely Cat-500-2-12, was computed to be 52.29 m/g. The crystallite size of titanium oxide on the optimum photocatalyst was calculated ~17.68 nm. The FTIR test confirmed the presence of C=C, O-H, C=O, C-S, and C-H functional groups in the photocatalyst. The transformation pathway for the degradation of cephalexin by the developed system was drawn. The present investigation showed that the developed technique (sea sediment/titanate-UV-HO-ultrasonic) could be used as a promising alternative for attenuating cephalexin from aqueous solutions.

摘要

本研究的目的是开发一种新的海泥/钛酸盐光催化剂,以在紫外 (UV) 光、过氧化氢 (HO) 和超声波存在的条件下去除水溶液中的头孢氨苄。探讨了炉温 (300、350、400 和 500°C)、炉停留时间 (1、2、3 和 4 小时) 和海泥:钛比 (0-6 v:w) 对海泥/钛酸盐光催化剂的物理化学性质和头孢氨苄去除率的影响。采用 FTIR、SEM/EDX、XRD、BET、BJH 和 Mapping 技术来确定所生成的光催化剂的物理化学性质。在炉温为 500°C、炉停留时间为 2 小时和海泥:钛比为 1:6(=12 mL TiO/2 g 海泥)的条件下,头孢氨苄的去除率最高(94.71%)。根据获得的结果,优化催化剂的比表面积计算为 52.29 m/g。最佳光催化剂上的氧化钛的晶粒尺寸计算为~17.68 nm。FTIR 测试证实了光催化剂中存在 C=C、O-H、C=O、C-S 和 C-H 官能团。绘制了开发系统降解头孢氨苄的转化途径。本研究表明,所开发的技术(海泥/钛酸盐-UV-HO-超声波)可以作为一种有前途的替代方法,用于从水溶液中去除头孢氨苄。

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