王志兵

个人信息

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教授     博士生导师     硕士生导师

教师英文名称:Zhibing Wang

教师拼音名称:wangzhibing

出生日期:1982-01-12

电子邮箱:

入职时间:2008-04-01

所在单位:长春工业大学化学与生命科学学院

职务:副院长

学历:研究生(博士)毕业

办公地点:南湖校区材料楼311

性别:男

联系方式:0431-85716470

学位:博士学位

在职信息:在职

毕业院校:吉林大学

学科:应用化学
生物学其他专业
分析化学
学术荣誉:
2018    学科带头人
2018    教学名师
曾获荣誉:
2023-04-26    吉林省高层次D类人才
2020-12-25    吉林省第二届高等学校教学新秀
2019-11-30    吉林省大学生生命科学竞赛优秀指导教师
2018-10-14    第十一届全国大学生创新创业年会优秀指导教师
2023-08-30    CULSC第八届全国大学生生命科学竞赛指导教师一等奖
2018-05-16    吉林省自然科学学术成果奖一等奖
2010-12-30    吉林省科学技术进步奖三等奖
2010-12-20    长春市科学技术进步奖三等奖
2008-06-08    吉林省高校科学技术研究优秀成果奖二等奖
2007-12-26    吉林省科学技术发明奖二等奖

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【SCI】Ionic liquid-based matrix solid-phase dispersion coupled with homogeneous liquid–liquid microextraction of synthetic dyes incondiments
发布时间:2021-06-28  点击次数:

所属单位:化学与生命科学学院
教研室:食品教研室
发表刊物:Journal of Chromatography A
项目来源:其他课题
关键字:Ionic liquid-based matrix solid-phase dispersion;Homogeneous liquid–liquid microextraction;Dyes;Condiments;High-performance liquid chromatography
摘要:tThe ionic liquid-based matrix solid-phase dispersion homogeneous liquid–liquid microextraction (IL-based MSPD–HLLME) was developed and applied to the extraction of four banned dyes, includingchrysoidin, safranine O, auramine O and rhodamine B, in condiment samples. High performance liquidchromatography was applied to the separation and determination of the analytes. The solid sample wasdirectly treated by MSPD using ionic liquid as dispersant and the eluate obtained in MSPD was treatedby HLLME. Some experimental parameters, including type of dispersant, ratio of sample to dispersant,type and volume of ionic liquid, type and volume of elution solvent, pH value and ionic strength of theelution solvent, amount of ion-pairing agent (NH4PF6) and extraction time, were investigated and opti-mized. The linearities for determining the analytes were in the range of 60–2000 g kg−1for chrysoidin,40–2000 g kg−1for safranine O and 20–1000 g kg−1for auramine O and rhodamine B, with the corre-lation coefficients ranging from 0.9964 to 0.9991. The limits of detection for the analytes were between6.7 and 26.8 g kg−1and the limits of quantification were between 15.99 and 58.48 g kg−1. When thepresent method was applied to the analysis of spiked condiment samples, the recoveries of the analytesranged from 90.69 to 113.52% and relative standard deviations were lower than 8.2%. The present methodcombined the advantages of MSPD and HLLME, and could be applied for the determination of syntheticdyes in condiment samples.
合写作者:张丽媛,李娜,雷蕾,邵明媛,杨潇,宋颖,于爱民,张寒琦,邱芳萍
第一作者:王志兵
论文类型:期刊论文
卷号:1348
页面范围:2
是否译文:否
发表时间:2014-01-27