首页> 外文学位 >Sol-gel zirconia- and titania-based surface-bonded hybrid organic-inorganic coatings for sample preconcentration and analysis via capillary microextraction in hyphenation with gas chromatography (CME-GC).
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Sol-gel zirconia- and titania-based surface-bonded hybrid organic-inorganic coatings for sample preconcentration and analysis via capillary microextraction in hyphenation with gas chromatography (CME-GC).

机译:溶胶-凝胶氧化锆和二氧化钛基表面键合杂化有机-无机涂料,用于样品预富集和通过毛细管微萃取在气相色谱(CME-GC)中进行联用分析。

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摘要

Novel zirconia- and titania-based sol-gel hybrid organic-inorganic coatings were developed for capillary microextraction (in-tube SPME). Principles of sol-gel chemistry were employed to chemically bind two hydroxy-terminated silicone polymers (polydimethyldiphenylsiloxane, PDMDPS, and polydimethylsiloxane, PDMS) to sol-gel zirconia and titania networks in the course of their evolution from highly reactive alkoxide precursors undergoing controlled hydrolytic polycondensation reactions. A properly designed sol solution was used to conduct the sol-gel reactions inside a fused silica capillary for ∼30 min to create a hybrid organic-inorganic sol-gel coating anchored to the capillary inner walls. The unbonded part of the sol solution was then expelled under helium pressure, and the coated capillary was conditioned under temperature programmed conditions. Aqueous samples containing parts per billion (ppb) level trace concentrations of polar and nonpolar analytes were passed through the sol-gel microextraction capillary using a gravity-fed sample dispenser. This process was continued for 30 min for extraction process to reach equilibrium. As the sample passed through the capillary, the target analyte molecules were sorbed and enriched by the sol-gel coating. The microextraction capillary (with the extracted analytes within the coating) was installed in a GC injection port with its exit end connected to the inlet of a sol-gel GC column. The extracted analytes were transferred from the microextraction capillary to the GC column using a rapid (100°C/min) temperature program in the injection port. The desorbed analytes were swept over by the carrier gas (helium) and were focused at the GC column inlet maintained at 30°C. GC analysis of the focused analytes were then performed by programming the column temperature. Parts per trillion (ppt) level detection limits were achieved for various classes of analytes by coupling CME with GC-FID. The newly developed sol-gel hybrid zirconia- and titania-based coatings demonstrated excellent pH stability, and retained the extraction characteristics intact even after continuous rinsing with a 0.1 M NaOH and/or 0.1 M HCl solution for 24 h. To our knowledge, this is the first report on the use of sol-gel zirconia- and titania-based hybrid organic-inorganic coatings as an extraction media in solid phase microextraction in hyphenation with gas chromatography.
机译:新型基于氧化锆和二氧化钛的溶胶-凝胶杂化有机-无机涂料被开发用于毛细管微萃取(管内SPME)。溶胶-凝胶化学原理被用来将两种羟基封端的有机硅聚合物(聚二甲基二苯基硅氧烷,PDMDPS和聚二甲基硅氧烷,PDMS)化学键合到氧化锆和二氧化钛溶胶-凝胶网络中,此过程是由高活性醇盐前体经历受控水解缩聚而演变而来的反应。使用适当设计的溶胶溶液在熔融石英毛细管内进行约30分钟的溶胶-凝胶反应,以形成固定在毛细管内壁上的有机-无机杂化溶胶-涂层。然后在氦气压力下排出溶胶溶液中未结合的部分,并在程序设定的温度下调节涂覆的毛细管。使用重力进样样品分配器将含有十亿分之几(ppb)痕量浓度的极性和非极性分析物的水性样品通过溶胶-凝胶微萃取毛细管。继续该过程30分钟,以使提取过程达到平衡。当样品通过毛细管时,目标分析物分子被溶胶-凝胶涂层吸附并富集。将微萃取毛细管(在涂层中有提取的分析物)安装在GC进样口中,其出口端连接到溶胶-凝胶GC柱的入口。使用进样口中的快速(100°C / min)温度程序将提取的分析物从微萃取毛细管转移到GC色谱柱。解吸的分析物被载气(氦气)吹扫,并聚焦在保持在30°C的GC色谱柱入口处。然后通过对色谱柱温度进行编程,对聚焦分析物进行GC分析。通过将CME与GC-FID结合使用,可以对各种类型的分析物实现万亿分之一(ppt)的检测限。新开发的溶胶-凝胶杂化氧化锆和二氧化钛基涂料具有出色的pH稳定性,即使在用0.1 M NaOH和/或0.1 M HCl溶液连续漂洗24小时后仍能保持萃取特性不变。就我们所知,这是关于使用溶胶-凝胶氧化锆和二氧化钛基杂化有机-无机涂层作为气相色谱联用固相微萃取中萃取介质的第一份报告。

著录项

  • 作者

    Alhooshani, Khalid R.;

  • 作者单位

    University of South Florida.;

  • 授予单位 University of South Florida.;
  • 学科 Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2005
  • 页码 239 p.
  • 总页数 239
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

  • 入库时间 2022-08-17 11:42:58

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