...
首页> 外文期刊>Analytical and bioanalytical chemistry >Electrospun composite of polypyrrole-polyamide as a micro-solid phase extraction sorbent
【24h】

Electrospun composite of polypyrrole-polyamide as a micro-solid phase extraction sorbent

机译:聚吡咯-聚酰胺作为微固相萃取吸附剂的电纺复合材料

获取原文
获取原文并翻译 | 示例
           

摘要

A micro-solid phase extraction technique was developed using a novel polypyrrole-polyamide nanofiber sheet, fabricated by electrospinning method. The applicability of the new nanofiber sheet was examined as an extracting medium to isolate malathion as a model pesticide from aqueous samples. Solvent desorption was subsequently performed in a microvial, and an aliquot of extractant was injected into gas chromatography-mass spectrometry. Various parameters affecting the electrospinning process including monomer concentration, polyamide content, applied voltage, and electrospinning time were examined. After fabricating the most suitable preparation conditions, influential parameters on the extraction and desorption processes were optimized. The developed method proved to be rather convenient and offers sufficient sensitivity and good reproducibility. The limit of detection (S/N∈=∈3) and limit of quantification (S/N∈=∈10) of the method under optimized conditions were 50 and 100 ng L~(-1), respectively. The relative standard deviation at concentration level of 1 ng mL~(-1) was 2% (n∈=∈3). The calibration curve of analyte showed linearity in the range of 0.1-1 ng mL~(-1) (R ~2∈=∈0.9975). The developed method was successfully applied to tap and Zayanderood river water samples, while the relative recovery percentages of 98% and 96% were obtained, respectively. The whole procedure showed to be conveniently applicable and quite easy to be manipulated. [Figure not available: see fulltext.]
机译:利用静电纺丝法制备的新型聚吡咯-聚酰胺纳米纤维片材开发了微固相萃取技术。研究了新纳米纤维片材作为提取介质从水性样品中分离马拉硫磷作为模型农药的适用性。随后在微瓶中进行溶剂解吸,并将等分的萃取剂注入气相色谱-质谱法。检查了影响静电纺丝工艺的各种参数,包括单体浓度,聚酰胺含量,施加电压和静电纺丝时间。制定最合适的制备条件后,对萃取和解吸过程中的影响参数进行了优化。事实证明,所开发的方法非常方便,并具有足够的灵敏度和良好的重现性。该方法在优化条件下的检出限(S /N∈=ε3)和定量限(S /N∈=ε10)分别为50 ng L〜(-1)。浓度水平为1 ng mL〜(-1)时的相对标准偏差为2%(n∈=∈3)。分析物的校正曲线在0.1-1 ng mL〜(-1)范围内呈线性关系(R〜2∈=∈0.9975)。所开发的方法已成功应用于自来水和Zayanderood河水样品,相对回收率分别为98%和96%。整个程序显示出方便的适用性和相当容易的操作。 [图不可用:请参见全文。]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号