• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

使用高铁酸盐(VI)/TiO 在紫外光照射下对来自塑料工业废水的邻苯二甲酸二甲酯(DMP)进行氧化降解/矿化。

Oxidative degradation/mineralization of dimethyl phthalate (DMP) from plastic industrial wastewater using ferrate(VI)/TiO under ultraviolet irradiation.

机构信息

College of Biology and the Environment, Nanjing Forestry University, Nanjing, 210037, Jiangsu, People's Republic of China.

出版信息

Environ Sci Pollut Res Int. 2022 Feb;29(10):15159-15171. doi: 10.1007/s11356-021-16636-x. Epub 2021 Oct 9.

DOI:10.1007/s11356-021-16636-x
PMID:34628611
Abstract

A novel ferrate(VI)/titanium dioxide/ultraviolet [Fe(VI)/TiO/UV] system was successfully established for the photocatalytic oxidation of dimethyl phthalate (DMP). This system demonstrated a higher removal efficiency of DMP (95.2%) than the conventional TiO/UV and Fe(VI) alone systems (51.8% and 23.5%, respectively) and produced obvious synergistic effects. Response surface methodology (RSM), based on a three level, three independent variables design, was conducted through Design Expert 8.0.6 program, and a second-order polynomial model (R = 0.998) was developed to quantitatively describe the photocatalysis of TiO combined with Fe(VI) oxidation under ultraviolet irradiation. The fresh TiO and photochemical reacted Fe(VI)/TiO were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and element dispersive spectrum (EDS), which indicated that Fe(VI) was imprinted into the TiO, and the surface adsorbed Fe-O-(organic) materials inhibited DMP degradation. This photocatalytic oxidant showed high activity and stability after nine cycles without loss of its effectiveness (counting from the second cycle). The intermediates/products of DMP were analyzed by gas chromatography-mass spectrometry. The proposed pathway for DMP degradation involved one electron transfer of hydroxyl radical and breaking of the ester bond and benzene ring. The mineralization efficiencies of DMP in actual industrial wastewater and simulated water were 87.1% and 95.2%, respectively, suggesting practical field applications. A ecotoxicity test (17.3% inhibition on bioluminescence) in treating actual industrial wastewater containing DMP implied that the proposed Fe(VI)/TiO/UV had a potential for industrial water treatment.

摘要

一种新型的高铁酸盐(VI)/二氧化钛/紫外线[Fe(VI)/TiO/UV]系统被成功建立,用于光催化氧化邻苯二甲酸二甲酯(DMP)。该系统对 DMP 的去除效率(95.2%)明显高于传统的 TiO/UV 和单独的 Fe(VI)系统(分别为 51.8%和 23.5%),并产生了明显的协同效应。响应面法(RSM)基于三水平、三独立变量设计,通过 Design Expert 8.0.6 程序进行,建立了一个二阶多项式模型(R = 0.998),定量描述了在紫外线照射下 TiO 与 Fe(VI)氧化的光催化作用。新鲜的 TiO 和光化学反应后的 Fe(VI)/TiO 采用 X 射线衍射(XRD)、扫描电子显微镜(SEM)和元素分散谱(EDS)进行了表征,结果表明 Fe(VI)被印迹到 TiO 中,表面吸附的 Fe-O-(有机)材料抑制了 DMP 的降解。这种光催化剂在经过九次循环后,没有失去其有效性(从第二次循环开始计算),仍然表现出很高的活性和稳定性。通过气相色谱-质谱联用仪分析了 DMP 的中间产物/产物。DMP 降解的途径涉及羟基自由基的一次电子转移和酯键和苯环的断裂。在实际工业废水和模拟水中,DMP 的矿化效率分别为 87.1%和 95.2%,表明该方法具有实际的应用前景。在处理含有 DMP 的实际工业废水时,生态毒性试验(对生物发光的 17.3%抑制)表明,所提出的 Fe(VI)/TiO/UV 具有工业水处理的潜力。

相似文献

1
Oxidative degradation/mineralization of dimethyl phthalate (DMP) from plastic industrial wastewater using ferrate(VI)/TiO under ultraviolet irradiation.使用高铁酸盐(VI)/TiO 在紫外光照射下对来自塑料工业废水的邻苯二甲酸二甲酯(DMP)进行氧化降解/矿化。
Environ Sci Pollut Res Int. 2022 Feb;29(10):15159-15171. doi: 10.1007/s11356-021-16636-x. Epub 2021 Oct 9.
2
Ferrate(VI) enhanced photocatalytic oxidation of pollutants in aqueous TiO2 suspensions.高铁酸盐(VI)增强的 TiO2 悬浮液中污染物的光催化氧化。
Environ Sci Pollut Res Int. 2010 Feb;17(2):453-61. doi: 10.1007/s11356-009-0170-0. Epub 2009 Jun 3.
3
Reaction pathways of dimethyl phthalate degradation in TiO2-UV-O2 and TiO2-UV-Fe(VI) systems.邻苯二甲酸二甲酯在TiO₂-UV-O₂和TiO₂-UV-Fe(VI)体系中的降解反应途径。
Chemosphere. 2008 May;72(2):197-204. doi: 10.1016/j.chemosphere.2008.01.055. Epub 2008 Mar 14.
4
Aqueous oxidation of dimethyl phthalate in a Fe(VI)-TiO(2)-UV reaction system.邻苯二甲酸二甲酯在Fe(VI)-TiO₂-UV反应体系中的水相氧化
Water Res. 2008 Mar;42(6-7):1413-20. doi: 10.1016/j.watres.2007.10.010. Epub 2007 Oct 13.
5
Photocatalytic degradation of dimethyl phthalate in an aqueous solution with Pt-doped TiO2-coated magnetic PMMA microspheres.用负载 Pt 的 TiO2 涂层磁性 PMMA 微球在水溶液中光催化降解邻苯二甲酸二甲酯。
J Hazard Mater. 2009 Dec 15;172(1):20-9. doi: 10.1016/j.jhazmat.2009.06.122. Epub 2009 Jun 30.
6
Oxidation of Sulfonamides in Aqueous Solution by UV-TiO2-Fe(VI).紫外光-二氧化钛-高铁酸盐(VI)对水溶液中磺胺类药物的氧化作用
Biomed Res Int. 2015;2015:973942. doi: 10.1155/2015/973942. Epub 2015 Aug 11.
7
Reduction of ferrate(VI) and oxidation of cyanate in a Fe(VI)-TiO2-UV-NCO- system.Fe(VI)-TiO2-UV-NCO体系中铁酸盐(VI)的还原及氰酸盐的氧化
Chemosphere. 2008 Aug;72(11):1694-9. doi: 10.1016/j.chemosphere.2008.05.008. Epub 2008 Jun 17.
8
Enhanced degradation of 2,6-dimethylphenol by photocatalytic systems using TiO assisted with HO and Fe(III).使用TiO并辅以HO和Fe(III)的光催化体系对2,6-二甲基苯酚的强化降解
Environ Technol. 2023 Apr;44(10):1464-1477. doi: 10.1080/09593330.2021.2005686. Epub 2021 Dec 1.
9
Photocatalytic ozonation of dimethyl phthalate with TiO2 prepared by a hydrothermal method.水热法制备 TiO2 光催化臭氧氧化邻苯二甲酸二甲酯。
J Hazard Mater. 2011 May 15;189(1-2):40-7. doi: 10.1016/j.jhazmat.2011.01.132. Epub 2011 Mar 3.
10
Enhanced photocatalytic reduction of Cr(VI) from aqueous solution using Fe/TiO-based polymeric nanocomposites.采用 Fe/TiO 基聚合物纳米复合材料增强水溶液中 Cr(VI)的光催化还原。
Environ Sci Pollut Res Int. 2023 Nov;30(51):110312-110323. doi: 10.1007/s11356-023-30106-6. Epub 2023 Oct 3.

引用本文的文献

1
Insights into the Photoelectrocatalytic Behavior of gCN-Based Anode Materials Supported on Ni Foams.泡沫镍负载的gCN基阳极材料的光电催化行为研究
Nanomaterials (Basel). 2023 Mar 13;13(6):1035. doi: 10.3390/nano13061035.
2
Peroxymonosulphate Activation by Basolite F-300 for Disinfection and Antipyrine Degradation.过一硫酸氢盐在 Basolite F-300 作用下的激活及其对消毒和安替比林的降解作用。
Int J Environ Res Public Health. 2022 Jun 3;19(11):6852. doi: 10.3390/ijerph19116852.