Combining microwave and ultraviolet energy for sample preparation of polymer-based materials for further halogen determination

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2022-10-01 DOI:10.1016/j.sampre.2022.100038
Alice P. Holkem , Gabrielle D. Iop , Gustavo R. Bitencourt , Erico M.M. Flores , Márcia F. Mesko , Paola A. Mello
{"title":"Combining microwave and ultraviolet energy for sample preparation of polymer-based materials for further halogen determination","authors":"Alice P. Holkem ,&nbsp;Gabrielle D. Iop ,&nbsp;Gustavo R. Bitencourt ,&nbsp;Erico M.M. Flores ,&nbsp;Márcia F. Mesko ,&nbsp;Paola A. Mello","doi":"10.1016/j.sampre.2022.100038","DOIUrl":null,"url":null,"abstract":"<div><p>In this work, a microwave-assisted ultraviolet wet digestion (MAWD-UV) protocol was used to digest polymer-based materials (e-waste, food packing, medical-care materials, and individual protection equipment) for further halogen determination. Digests were suitable for Cl, Br, and I determination by inductively coupled plasma mass spectrometry (ICP-MS) or inductively coupled plasma optical emission spectrometry (ICP-OES). Fluorine determination was performed with ion selective electrode (ISE). The power radiation and the digestion solution were evaluated. The accuracy was evaluated by comparing the results with those obtained after neutron activation analysis (NAA) for Cl and Br or using microwave-induced combustion (MIC) as sample preparation for F and I. Two certified reference materials (CRM) of low-density polyethylene (ERM EC680k and EC681k) were evaluated, and no differences were observed (<em>t</em>-test, 95% confidence level) between the results and the certified values. Quantitative recoveries for Cl, Br, and I were obtained using 200 mg of the sample using diluted acid solution (15 mL of 0.5 mol L<sup>−1</sup> HNO<sub>3</sub> plus 10.6 mol L<sup>−1</sup> of H<sub>2</sub>O<sub>2</sub>), with a 40 min radiation program (700 W, 25 min ramp). No statistical differences (ANOVA, 95% confidence level) were observed between the MAWD-UV and ICP-MS results and the reference values for Cl, Br, and I for several samples. However, results were lower than the reference values for fluorine, indicating that digestion efficiency was poor for this analyte, which was probably as an organic molecule (likely polytetrafluoroethylene). The limit of quantification (LOQ) was 0.216 mg g<sup>−1</sup> for Cl, 3.33 µg g<sup>−1</sup> for Br, and 0.036 µg g<sup>−1</sup> for I using ICP-MS. The main advantage of MAWD-UV is that it enables decomposing several polymer-based matrices using diluted acid without halogen losses. The developed method represents an important contribution to the digestion of these hard-to-digest matrices and in compliance with green analytical chemistry, thereby being an advance in sample preparation.</p></div>","PeriodicalId":100052,"journal":{"name":"Advances in Sample Preparation","volume":"4 ","pages":"Article 100038"},"PeriodicalIF":5.2000,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772582022000353/pdfft?md5=9172df7e09c50ff85ea0f156b3553e74&pid=1-s2.0-S2772582022000353-main.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Sample Preparation","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772582022000353","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 1

Abstract

In this work, a microwave-assisted ultraviolet wet digestion (MAWD-UV) protocol was used to digest polymer-based materials (e-waste, food packing, medical-care materials, and individual protection equipment) for further halogen determination. Digests were suitable for Cl, Br, and I determination by inductively coupled plasma mass spectrometry (ICP-MS) or inductively coupled plasma optical emission spectrometry (ICP-OES). Fluorine determination was performed with ion selective electrode (ISE). The power radiation and the digestion solution were evaluated. The accuracy was evaluated by comparing the results with those obtained after neutron activation analysis (NAA) for Cl and Br or using microwave-induced combustion (MIC) as sample preparation for F and I. Two certified reference materials (CRM) of low-density polyethylene (ERM EC680k and EC681k) were evaluated, and no differences were observed (t-test, 95% confidence level) between the results and the certified values. Quantitative recoveries for Cl, Br, and I were obtained using 200 mg of the sample using diluted acid solution (15 mL of 0.5 mol L−1 HNO3 plus 10.6 mol L−1 of H2O2), with a 40 min radiation program (700 W, 25 min ramp). No statistical differences (ANOVA, 95% confidence level) were observed between the MAWD-UV and ICP-MS results and the reference values for Cl, Br, and I for several samples. However, results were lower than the reference values for fluorine, indicating that digestion efficiency was poor for this analyte, which was probably as an organic molecule (likely polytetrafluoroethylene). The limit of quantification (LOQ) was 0.216 mg g−1 for Cl, 3.33 µg g−1 for Br, and 0.036 µg g−1 for I using ICP-MS. The main advantage of MAWD-UV is that it enables decomposing several polymer-based matrices using diluted acid without halogen losses. The developed method represents an important contribution to the digestion of these hard-to-digest matrices and in compliance with green analytical chemistry, thereby being an advance in sample preparation.

Abstract Image

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
结合微波和紫外线能量制备聚合物基材料,进一步测定卤素
在这项工作中,采用微波辅助紫外湿消解(MAWD-UV)方案来消解聚合物基材料(电子垃圾、食品包装、医疗保健材料和个人防护设备),以进一步测定卤素。消化物适用于电感耦合等离子体质谱法(ICP-MS)或电感耦合等离子体发射光谱法(ICP-OES)测定Cl、Br和I。采用离子选择电极(ISE)测定氟。对功率辐射和溶出液进行了评价。通过与中子活化分析(NAA)测定Cl和Br或微波诱导燃烧(MIC)制备F和i的结果进行比较,评估了两种低密度聚乙烯(ERM EC680k和EC681k)的认证标准物质(CRM)的准确性,结果与认证值之间没有差异(t检验,95%置信水平)。使用稀释的酸溶液(15ml 0.5 mol L−1 HNO3 + 10.6 mol L−1 H2O2)取200mg样品,辐射程序(700 W, 25 min斜坡)40 min,获得Cl, Br和I的定量回收率。在一些样品中,MAWD-UV和ICP-MS的结果与Cl、Br和I的参考值之间没有统计学差异(方差分析,95%置信水平)。然而,结果低于氟的参考值,表明该分析物的消化效率较差,可能是作为有机分子(可能是聚四氟乙烯)。ICP-MS的定量限(LOQ)为Cl 0.216 mg g−1,Br 3.33 μ g g−1,I 0.036 μ g g−1。MAWD-UV的主要优点是它可以使用稀释的酸分解几种聚合物基基质而不会损失卤素。开发的方法代表了消化这些难以消化的基质的重要贡献,并符合绿色分析化学,因此是样品制备的一个进步。
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
CiteScore
3.50
自引率
0.00%
发文量
0
期刊最新文献
Determination of steroid hormones in sea urchins by microwave-assisted extraction and ultrahigh-performance liquid chromatography tandem mass spectrometry Extraction of synthetic cathinones from biological samples: A systematic review Microextraction by packed sorbent: Introducing a novel hybrid silica-based chitosan-graphene oxide biosorbent for the evaluation of pesticides and antibiotics in food matrices One step derivatization and switchable hydrophilicity solvent-based microextraction for the determination of adamantane analogues in human urine by HPLC-FLD Recent advances in the application of MOFs and COFs composites for sample preparation
×
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