Interconversion and Removal of Inorganic Nitrogen Compounds via UV Irradiation

IF 2.8 Q2 ENGINEERING, CHEMICAL ChemEngineering Pub Date : 2023-08-31 DOI:10.3390/chemengineering7050079
Alejandro M. Senn, N. Quici
{"title":"Interconversion and Removal of Inorganic Nitrogen Compounds via UV Irradiation","authors":"Alejandro M. Senn, N. Quici","doi":"10.3390/chemengineering7050079","DOIUrl":null,"url":null,"abstract":"Dissolved inorganic nitrogen (DIN) species are key components of the nitrogen cycle and are the main nitrogen pollutants in groundwater. This study investigated the interconversion and removal of the principal DIN compounds (NO3−, NO2− and NH4+) via UV light irradiation using a medium-pressure mercury lamp. The experiments were carried out systematically at relatively low nitrogen concentrations (1.5 mM) at varying pHs in the presence and absence of oxygen to compare the reaction rates and suggest the reaction mechanisms. NO3− was fully converted into NO2− at a pH > 3 in both oxic and anoxic conditions, and the reaction was faster when the pH was increased following a first-order kinetic at pH 11 (k = 0.12 min−1, R2 = 0.9995). NO2− was partially converted into NO3− only at pH 3 and in the presence of oxygen and was stable at an alkaline pH. This interconversion of NO3− and NO2− did not yield nitrogen loss in the solution. The addition of formic acid as an electron donor led to the reduction of NO3− to NH4+. Conversely, NH4+ was converted into NO2−, NO3− and to an unidentified subproduct in the presence of O2  at pH 10. Finally, it was demonstrated that NO2− and NH4+ react via UV irradiation with stoichiometry 1:1 at pH 10 with the total loss of nitrogen in the solution. With these results, a strategy to remove DIN compounds via UV irradiation was proposed with the eventual use of solar light.","PeriodicalId":9755,"journal":{"name":"ChemEngineering","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2023-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemEngineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/chemengineering7050079","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Dissolved inorganic nitrogen (DIN) species are key components of the nitrogen cycle and are the main nitrogen pollutants in groundwater. This study investigated the interconversion and removal of the principal DIN compounds (NO3−, NO2− and NH4+) via UV light irradiation using a medium-pressure mercury lamp. The experiments were carried out systematically at relatively low nitrogen concentrations (1.5 mM) at varying pHs in the presence and absence of oxygen to compare the reaction rates and suggest the reaction mechanisms. NO3− was fully converted into NO2− at a pH > 3 in both oxic and anoxic conditions, and the reaction was faster when the pH was increased following a first-order kinetic at pH 11 (k = 0.12 min−1, R2 = 0.9995). NO2− was partially converted into NO3− only at pH 3 and in the presence of oxygen and was stable at an alkaline pH. This interconversion of NO3− and NO2− did not yield nitrogen loss in the solution. The addition of formic acid as an electron donor led to the reduction of NO3− to NH4+. Conversely, NH4+ was converted into NO2−, NO3− and to an unidentified subproduct in the presence of O2  at pH 10. Finally, it was demonstrated that NO2− and NH4+ react via UV irradiation with stoichiometry 1:1 at pH 10 with the total loss of nitrogen in the solution. With these results, a strategy to remove DIN compounds via UV irradiation was proposed with the eventual use of solar light.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
紫外辐照下无机氮化合物的相互转化和去除
溶解无机氮(DIN)是氮循环的关键组成部分,也是地下水中主要的氮污染物。本研究使用中压汞灯通过紫外线照射研究了主要DIN化合物(NO3−、NO2−和NH4+)的相互转化和去除。在存在和不存在氧气的情况下,在相对较低的氮浓度(1.5mM)和不同的pH下系统地进行实验,以比较反应速率并提出反应机制。在好氧和缺氧条件下,当pH>3时,NO3−完全转化为NO2−,并且当pH在pH 11时按照一级动力学增加时反应更快(k=0.12 min−1,R2=0.9995)。NO2−仅在pH 3和氧气存在下部分转化为NO3−,并且在碱性pH下稳定。NO3−和NO2−的这种相互转化在溶液中没有产生氮损失。甲酸作为电子供体的加入导致NO3−还原为NH4+。相反,在pH为10的O2存在下,NH4+转化为NO2−、NO3−并转化为未识别的子产物。最后,证明了NO2−和NH4+在pH为10时通过化学计量为1:1的紫外线照射反应,溶液中氮的总损失。根据这些结果,提出了一种通过紫外线照射去除DIN化合物的策略,最终使用太阳能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
ChemEngineering
ChemEngineering Engineering-Engineering (all)
CiteScore
4.00
自引率
4.00%
发文量
88
审稿时长
11 weeks
期刊最新文献
Catalysts Based on Iron Oxides for Wastewater Purification from Phenolic Compounds: Synthesis, Physicochemical Analysis, Determination of Catalytic Activity Effect of Inserting Baffles on the Solid Particle Segregation Behavior in Fluidized Bed Reactor: A Computational Study Force Field for Calculation of the Vapor-Liquid Phase Equilibrium of trans-Decalin Antisolvent Crystallization of Papain Ultrafiltration to Increase the Consistency of Fruit Pulps: The Role of Permeate Flux
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1