Boric Acid Detection in Water by Gallacetophenone

Kai Sato, H. Kimoto, T. Hashimoto, T. Hayashita
{"title":"Boric Acid Detection in Water by Gallacetophenone","authors":"Kai Sato, H. Kimoto, T. Hashimoto, T. Hayashita","doi":"10.5182/jaie.33.100","DOIUrl":null,"url":null,"abstract":"The detection of boron down to ppt order in ultrapure water is required to ensure high-quality and stable semiconductor manufacturing. To realize a simple yet sensitive method for the detection of boron (boric acid), we designed a ruthenium complex possessing a stable ligand with boric acid sensing function. Gallacetophenone (2’,3’,4’-trihydroxyacetophenone) ligand has a b -diketone moiety that can coordinate to a metal and a cis -diol moiety that shows reactivity with boric acid. Comparison of UV-vis absorption spectra measured in the presence and absence of boric acid at various pH revealed that gallacetophenone showed the greatest response to boric acid at pH 8.58. From the spectral changes in the absorbance of gallacetophenone aqueous solution in various concentrations of boric acid at pH 8.58, decreases in the absorbance at the wavelength of 330 nm were observed with increasing boric acid concentration. On the basis of the relationship between the absorption spectra and the boric acid concentration, the binding constant (assuming a 1:1 binding model) for the interaction between gallacetophenone and boric acid was estimated to be 420.7 ± 28.0 mol -1 dm 3 . The electrochemical detection of boric acid was also conducted.","PeriodicalId":16331,"journal":{"name":"Journal of ion exchange","volume":"81 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of ion exchange","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5182/jaie.33.100","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

The detection of boron down to ppt order in ultrapure water is required to ensure high-quality and stable semiconductor manufacturing. To realize a simple yet sensitive method for the detection of boron (boric acid), we designed a ruthenium complex possessing a stable ligand with boric acid sensing function. Gallacetophenone (2’,3’,4’-trihydroxyacetophenone) ligand has a b -diketone moiety that can coordinate to a metal and a cis -diol moiety that shows reactivity with boric acid. Comparison of UV-vis absorption spectra measured in the presence and absence of boric acid at various pH revealed that gallacetophenone showed the greatest response to boric acid at pH 8.58. From the spectral changes in the absorbance of gallacetophenone aqueous solution in various concentrations of boric acid at pH 8.58, decreases in the absorbance at the wavelength of 330 nm were observed with increasing boric acid concentration. On the basis of the relationship between the absorption spectra and the boric acid concentration, the binding constant (assuming a 1:1 binding model) for the interaction between gallacetophenone and boric acid was estimated to be 420.7 ± 28.0 mol -1 dm 3 . The electrochemical detection of boric acid was also conducted.
没食子苯乙酮检测水中硼酸
为了保证半导体制造的高质量和稳定性,需要在超纯水中检测到低至ppt级的硼。为了实现一种简单而灵敏的检测硼(硼酸)的方法,我们设计了一种具有稳定配体和硼酸传感功能的钌配合物。没食子苯乙酮(2 ',3 ',4 ' -三羟基苯乙酮)配体具有b -二酮部分,可与金属配位,具有顺式二醇部分,可与硼酸反应。比较不同pH值下硼酸存在和不存在时的紫外-可见吸收光谱结果表明,当pH值为8.58时,没食子苯乙酮对硼酸的响应最大。从pH为8.58时不同浓度硼酸对没食子苯酮水溶液吸光度的光谱变化来看,随着硼酸浓度的增加,330 nm处的吸光度降低。根据吸收光谱与硼酸浓度的关系,估计没食子苯乙酮与硼酸相互作用的结合常数(假设为1:1结合模型)为420.7±28.0 mol -1 dm 3。并对硼酸进行了电化学检测。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信