Malathion determination in Rice samples with Graphene oxide reinforced hollow fiber-solid phase microextraction by GC-MASS

IF 2.4 Q3 CHEMISTRY, MULTIDISCIPLINARY
B. Sefati, M. Masrournia, Z. Es’haghi, M. Bozorgmehr
{"title":"Malathion determination in Rice samples with Graphene oxide reinforced hollow fiber-solid phase microextraction by GC-MASS","authors":"B. Sefati, M. Masrournia, Z. Es’haghi, M. Bozorgmehr","doi":"10.48317/IMIST.PRSM/MORJCHEM-V8I3.21644","DOIUrl":null,"url":null,"abstract":"A method for applicability of the solid phase microextraction (SPME) procedure for determination of trace amounts of the organophosphorus pesticide malathion by gas chromatography - mass spectrometry (GC-MS) was developed. Graphene oxide reinforced sol–gel which was placed in hollow fiber (HF-SPME) was used for pre-concentration of malathion. In the present study the Plackett-Burman (PB) factorial design was used as a method for first monitoring of Eight factors that have a significant impact and optimized them in next stage, optimization process of significant factor was carried out using a five-level CCD after screening by PBD. the following conditions were selected for the analytical method of Malathion in real sample: amount of GO (0.01gr), pH of aqueous solution (pH: 3), volume of aqueous solution (10000 µl), volume of organic solvent (250 µl), adsorption time (35 min), desorption time (30 min), stirring rate of solution (1000 rpm) and amount of salt (4%). Calibration curves were plotted using three spiking levels of malathion in the concentration ranges of 0.2–0.4-0.5 ng/mL with correlation coefficients (r 2 ) 0.9914 for analytes. Under the optimized extraction conditions, the method showed good linearity (0.05–0.5 ng/mL), repeatability, low limits of detections (3.9×10 -3 ng/mL) and excellent pre-concentration factors (4000). The optimum conditions which were evaluated then applied for the analysis of malathion in the rice as a real sample","PeriodicalId":18768,"journal":{"name":"Moroccan Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2020-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Moroccan Journal of Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.48317/IMIST.PRSM/MORJCHEM-V8I3.21644","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

A method for applicability of the solid phase microextraction (SPME) procedure for determination of trace amounts of the organophosphorus pesticide malathion by gas chromatography - mass spectrometry (GC-MS) was developed. Graphene oxide reinforced sol–gel which was placed in hollow fiber (HF-SPME) was used for pre-concentration of malathion. In the present study the Plackett-Burman (PB) factorial design was used as a method for first monitoring of Eight factors that have a significant impact and optimized them in next stage, optimization process of significant factor was carried out using a five-level CCD after screening by PBD. the following conditions were selected for the analytical method of Malathion in real sample: amount of GO (0.01gr), pH of aqueous solution (pH: 3), volume of aqueous solution (10000 µl), volume of organic solvent (250 µl), adsorption time (35 min), desorption time (30 min), stirring rate of solution (1000 rpm) and amount of salt (4%). Calibration curves were plotted using three spiking levels of malathion in the concentration ranges of 0.2–0.4-0.5 ng/mL with correlation coefficients (r 2 ) 0.9914 for analytes. Under the optimized extraction conditions, the method showed good linearity (0.05–0.5 ng/mL), repeatability, low limits of detections (3.9×10 -3 ng/mL) and excellent pre-concentration factors (4000). The optimum conditions which were evaluated then applied for the analysis of malathion in the rice as a real sample
氧化石墨烯增强中空纤维-气相色谱-质谱法测定大米样品中的马拉硫磷
建立了固相微萃取(SPME)气相色谱-质谱(GC-MS)法测定有机磷农药马拉硫磷的适用性方法。将氧化石墨烯增强的溶胶-凝胶置于中空纤维(HF-SPME)中,用于马拉硫磷的预浓缩。在本研究中,使用Plackett-Burman(PB)因子设计作为对具有显著影响的八个因素进行首次监测的方法,并在下一阶段对其进行优化,在PBD筛选后,使用五级CCD对显著因素进行优化过程。马拉硫磷在真实样品中的分析方法选择了以下条件:GO的量(0.01gr)、水溶液的pH(pH:3)、水溶体的体积(10000µl)、有机溶剂的体积(250µl),吸附时间(35分钟)、解吸时间(30分钟)、溶液的搅拌速度(1000 rpm)和盐的量(4%)。使用0.2–0.4-0.5 ng/mL浓度范围内的三种马拉硫磷加标水平绘制校准曲线,分析物的相关系数(r2)为0.9914。在优化的提取条件下,该方法具有良好的线性(0.05–0.5 ng/mL)、重复性、低检测限(3.9×10-3 ng/mL)和良好的预浓缩因子(4000)。然后将评价的最佳条件应用于实际样品大米中马拉硫磷的分析
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
Moroccan Journal of Chemistry
Moroccan Journal of Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
3.40
自引率
9.10%
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