• 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

化学和热活化过硫酸盐用于茶碱降解及其在制药厂废水中的应用。

Chemically and thermally activated persulfate for theophylline degradation and application to pharmaceutical factory effluent.

作者信息

Al Hakim Suha, Baalbaki Abbas, Tantawi Omar, Ghauch Antoine

机构信息

American University of Beirut, Faculty of Arts and Sciences, Department of Chemistry P.O. Box 11-0236 Riad El Solh 1107-2020 Beirut Lebanon

出版信息

RSC Adv. 2019 Oct 18;9(57):33472-33485. doi: 10.1039/c9ra05362j. eCollection 2019 Oct 15.

DOI:10.1039/c9ra05362j
PMID:35529119
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9073359/
Abstract

Degradation of PPCPs by AOPs has gained major interest in the past decade. In this work, theophylline (TP) oxidation was studied in thermally (TAP) and chemically (CAP) activated persulfate systems, separately and in combination (TCAP). For [TP] = 10 mg L, (i) TAP resulted in 60% TP degradation at [PS] = 5 mM and = 60 °C after 60 min of reaction and (ii) CAP showed slight degradation at room temperature; however, (iii) TCAP resulted in complete TP degradation for [PS] = [Fe] = 2 mM at = 60 °C following a pseudo-first order reaction rate with calculated = 5.6 (±0.4) × 10 min. In the TCAP system, the [PS] : [Fe] ratio of 1 : 1 presented the best results. A positive correlation was obtained between the TP degradation rate and increasing temperature and [PS], and a negative correlation was obtained with increasing pH. Both chloride and humic acid inhibited the degradation process, while nitrates enhanced it. TP dissolved in spring, sea and waste water simulating real effluents showed lower degradation rates than in DI water. Waste water caused the highest inhibition ( = 2.6 (±0.6) × 10 min). Finally, the TCAP system was tested on a real factory effluent highly charged with TP, [TP] = 160 mg L, with successful degradation under the conditions of 60 °C and [PS] = [Fe] = 50 mM.

摘要

在过去十年中,高级氧化工艺(AOPs)对持久性有机污染物(PPCPs)的降解引起了人们的极大兴趣。在这项工作中,分别对热活化过硫酸盐(TAP)体系和化学活化过硫酸盐(CAP)体系以及二者联用(TCAP)体系中茶碱(TP)的氧化进行了研究。对于[TP]=10mg/L,(i)在反应60分钟后,当[PS]=5mM且温度=60℃时,TAP体系使TP降解了60%;(ii)CAP体系在室温下显示出轻微降解;然而,(iii)在60℃下,对于[PS]=[Fe]=2mM的TCAP体系,TP按照假一级反应速率完全降解,计算得到的速率常数=5.6(±0.4)×10⁻³min⁻¹。在TCAP体系中,[PS]∶[Fe]比例为1∶1时效果最佳。TP降解速率与温度升高和[PS]增加呈正相关,与pH升高呈负相关。氯化物和腐殖酸均抑制降解过程,而硝酸盐则促进降解。溶解在模拟实际废水的泉水、海水和废水中的TP的降解速率低于去离子水中的降解速率。废水造成的抑制作用最强(=2.6(±0.6)×10⁻³min⁻¹)。最后,在含有高浓度TP([TP]=160mg/L)的实际工厂废水中对TCAP体系进行了测试,在60℃和[PS]=[Fe]=50mM的条件下成功实现了降解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/92ce6ad560c5/c9ra05362j-f12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/998dcaf4647e/c9ra05362j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/8390486d7464/c9ra05362j-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/ab66f429d18f/c9ra05362j-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/164b8dd3c7f4/c9ra05362j-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/9a5043ccb412/c9ra05362j-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/3dcd6e93c32e/c9ra05362j-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/8e2489d379da/c9ra05362j-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/55f27a123aa2/c9ra05362j-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/239f4ef0e347/c9ra05362j-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/609e1a7bdeef/c9ra05362j-f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/542c2c5a08f5/c9ra05362j-f11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/92ce6ad560c5/c9ra05362j-f12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/998dcaf4647e/c9ra05362j-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/8390486d7464/c9ra05362j-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/ab66f429d18f/c9ra05362j-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/164b8dd3c7f4/c9ra05362j-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/9a5043ccb412/c9ra05362j-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/3dcd6e93c32e/c9ra05362j-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/8e2489d379da/c9ra05362j-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/55f27a123aa2/c9ra05362j-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/239f4ef0e347/c9ra05362j-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/609e1a7bdeef/c9ra05362j-f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/542c2c5a08f5/c9ra05362j-f11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8556/9073359/92ce6ad560c5/c9ra05362j-f12.jpg

相似文献

1
Chemically and thermally activated persulfate for theophylline degradation and application to pharmaceutical factory effluent.化学和热活化过硫酸盐用于茶碱降解及其在制药厂废水中的应用。
RSC Adv. 2019 Oct 18;9(57):33472-33485. doi: 10.1039/c9ra05362j. eCollection 2019 Oct 15.
2
Data for persulfate activation by UV light to degrade theophylline in a water effluent.通过紫外线激活过硫酸盐降解废水中茶碱的数据。
Data Brief. 2019 Oct 7;27:104614. doi: 10.1016/j.dib.2019.104614. eCollection 2019 Dec.
3
Degradation of the earthy and musty odorant 2,4,6-tricholoroanisole by persulfate activated with iron of different valences.不同价态铁活化过硫酸盐对土霉臭气味物质 2,4,6-三氯苯甲醚的降解。
Environ Sci Pollut Res Int. 2018 Feb;25(4):3435-3445. doi: 10.1007/s11356-017-0452-x. Epub 2017 Nov 19.
4
Degradation and mechanism of 2,4-dichlorophenoxyacetic acid (2,4-D) by thermally activated persulfate oxidation.热激活过硫酸盐氧化降解 2,4-二氯苯氧乙酸(2,4-D)及其机制。
Chemosphere. 2018 Dec;212:784-793. doi: 10.1016/j.chemosphere.2018.08.127. Epub 2018 Aug 28.
5
Oxidative degradation of diclofenac by thermally activated persulfate: implication for ISCO.热活化过硫酸盐对双氯芬酸的氧化降解:对原位化学氧化修复的意义
Environ Sci Pollut Res Int. 2016 Feb;23(4):3824-33. doi: 10.1007/s11356-015-5630-0. Epub 2015 Oct 26.
6
Evaluation of sulfathiazole degradation by persulfate in Milli-Q water and in effluent of a sewage treatment plant.过硫酸盐在超纯水中和污水处理厂废水中对磺胺噻唑降解的评估。
Environ Sci Pollut Res Int. 2017 Mar;24(7):6270-6277. doi: 10.1007/s11356-016-7036-z. Epub 2016 Jun 11.
7
Ultrasound and heat enhanced persulfate oxidation activated with Fe(0) aggregate for the decolorization of C.I. Direct Red 23.超声和热增强零价铁团聚物活化过硫酸盐氧化法对 C.I.直接红 23 的脱色作用。
Ultrason Sonochem. 2016 Mar;29:11-8. doi: 10.1016/j.ultsonch.2015.08.012. Epub 2015 Aug 24.
8
Degradation of MDEA in aqueous solution in the thermally activated persulfate system.热活化过硫酸盐体系中水溶液中甲基二乙醇胺(MDEA)的降解
Environ Technol. 2017 Mar;38(6):730-736. doi: 10.1080/09593330.2016.1210239. Epub 2016 Jul 25.
9
Degradation of carbon tetrachloride in aqueous solution in the thermally activated persulfate system.在热激活过硫酸盐体系中水溶液中四氯化碳的降解。
J Hazard Mater. 2015 Apr 9;286:7-14. doi: 10.1016/j.jhazmat.2014.12.031. Epub 2014 Dec 19.
10
Potential for activated persulfate degradation of BTEX contamination.过硫酸盐活化降解BTEX污染物的潜力。
Water Res. 2008 Sep;42(15):4091-100. doi: 10.1016/j.watres.2008.06.022. Epub 2008 Jun 29.

引用本文的文献

1
Peroxymonosulfate activation by Fe-Mn Co-doped biochar for carbamazepine degradation.铁锰共掺杂生物炭活化过一硫酸盐降解卡马西平
RSC Adv. 2024 Jan 2;14(2):1141-1149. doi: 10.1039/d3ra06065a.
2
Stability performance analysis of Fe based MOFs for peroxydisulfates activation to effectively degrade ciprofloxacin.用于过二硫酸盐活化以有效降解环丙沙星的铁基金属有机框架材料的稳定性性能分析
Front Bioeng Biotechnol. 2023 Jul 28;11:1205911. doi: 10.3389/fbioe.2023.1205911. eCollection 2023.
3
Degradation of ciprofloxacin by persulfate activated with pyrite: mechanism, acidification and tailwater reuse.

本文引用的文献

1
Oxidative degradation of atenolol by heat-activated persulfate: Kinetics, degradation pathways and distribution of transformation intermediates.热活化过硫酸盐对阿替洛尔的氧化降解:动力学、降解途径和转化中间产物的分布。
Chemosphere. 2018 Sep;207:174-182. doi: 10.1016/j.chemosphere.2018.05.068. Epub 2018 May 17.
2
Degradation of Penicillin G by heat activated persulfate in aqueous solution.水溶液中热激活过硫酸盐对青霉素 G 的降解。
J Environ Manage. 2018 Jun 1;215:316-323. doi: 10.1016/j.jenvman.2018.03.038.
3
Mineralization of naphtenic acids with thermally-activated persulfate: The important role of oxygen.
用黄铁矿活化过硫酸盐降解环丙沙星:机理、酸化及尾水回用
RSC Adv. 2022 Oct 20;12(46):29991-30000. doi: 10.1039/d2ra05412d. eCollection 2022 Oct 17.
萘酸的热活化过硫酸盐矿化:氧的重要作用。
J Hazard Mater. 2016 Nov 15;318:355-362. doi: 10.1016/j.jhazmat.2016.07.009. Epub 2016 Jul 6.
4
Lessons learned from more than two decades of research on emerging contaminants in the environment.从二十多年来对环境中新兴污染物的研究中吸取的教训。
J Hazard Mater. 2016 Oct 5;316:242-51. doi: 10.1016/j.jhazmat.2016.04.058. Epub 2016 Apr 25.
5
Activated persulfate for organic chemical degradation: A review.用于有机化学降解的活化过硫酸盐:综述
Chemosphere. 2016 May;151:178-88. doi: 10.1016/j.chemosphere.2016.02.055. Epub 2016 Mar 15.
6
Application of activated persulfate for removal of intermediates from antipyrine wastewater degradation refractory towards hydroxyl radical.过硫酸盐在去除羟基自由基难降解安替比林废水中中间产物的应用。
J Hazard Mater. 2016 Apr 5;306:77-86. doi: 10.1016/j.jhazmat.2015.12.001. Epub 2015 Dec 7.
7
Kinetic and mechanistic investigations of the degradation of sulfamethazine in heat-activated persulfate oxidation process.在热激活过硫酸盐氧化过程中降解磺胺甲恶唑的动力学和机理研究。
J Hazard Mater. 2015 Dec 30;300:39-47. doi: 10.1016/j.jhazmat.2015.06.058. Epub 2015 Jun 27.
8
Urine excretion of caffeine and select caffeine metabolites is common in the U.S. population and associated with caffeine intake.在美国人群中,咖啡因及其某些代谢产物通过尿液排泄的情况很常见,且与咖啡因摄入量有关。
J Nutr. 2015 Apr;145(4):766-74. doi: 10.3945/jn.114.205476. Epub 2015 Feb 4.
9
Tackling antibiotic resistance: the environmental framework.应对抗生素耐药性:环境框架。
Nat Rev Microbiol. 2015 May;13(5):310-7. doi: 10.1038/nrmicro3439. Epub 2015 Mar 30.
10
Hydroxyl radical induced oxidation of theophylline in water: a kinetic and mechanistic study.水中羟基自由基引发的茶碱氧化:动力学与机理研究
Org Biomol Chem. 2014 Aug 14;12(30):5611-20. doi: 10.1039/c4ob00102h. Epub 2014 Jun 24.