Fresco-Cala Beatriz, Cárdenas Soledad, Valcárcel Miguel
Department of Analytical Chemistry, Institute of Fine Chemistry and Nanotechnology, Marie Curie Building, Campus of Rabanales, University of Córdoba, 14071 Córdoba, Spain.
Department of Analytical Chemistry, Institute of Fine Chemistry and Nanotechnology, Marie Curie Building, Campus of Rabanales, University of Córdoba, 14071 Córdoba, Spain.
J Chromatogr A. 2016 Oct 14;1468:55-63. doi: 10.1016/j.chroma.2016.09.047. Epub 2016 Sep 22.
A novel hybrid micro and meso porous silica monolith with embedded carbon nanoparticles (Si-CNPs monolith) was prepared inside a fused silica capillary (3cm in length) and used as a sorbent for solid-phase microextraction. The hybrid monolithic capillary was synthetized by hydrolysis and polycondensation of a mixture of tetraethoxysilane (TEOS), ethanol, and three different carbon nanoparticles such as carboxylated single-walled carbon nanotubes (c-SWCNTs), carboxylated multi-walled carbon nanotubes (c-MWCNTs), and oxidized single-walled carbon nanohorns (o-SWNHs) via a two-step catalytic sol-gel process. Compared with silica monolith without carbon nanoparticles, the developed monolithic capillary column exhibited a higher extraction efficiency towards the analytes which can be ascribed to the presence of the carbon nanoparticles. In this regard, the best performance was achieved for silica monolith with embedded c-MWCNTs. The resulted monolithic capillaries were also characterized by scanning electron microscopy (SEM), elemental analysis and nitrogen intrusion porosimetry. Variables affecting to the preparation of the sorbent phase including three different carbon nanoparticles and extraction parameters were studied in depth using polycyclic aromatic hydrocarbons (PAHs) as target analytes. Gas chromatography-mass spectrometry was selected as instrumental technique. Detection limits range from 0.1 to 0.3μgL, and the inter-extraction units precision (expressed as relative standard deviation) is between 5.9 and 14.4%.
在熔融石英毛细管(长度为3厘米)内制备了一种新型的嵌入碳纳米颗粒的微-介孔混合二氧化硅整体柱(Si-CNPs整体柱),并将其用作固相微萃取的吸附剂。通过两步催化溶胶-凝胶法,使四乙氧基硅烷(TEOS)、乙醇和三种不同的碳纳米颗粒(如羧基化单壁碳纳米管(c-SWCNTs)、羧基化多壁碳纳米管(c-MWCNTs)和氧化单壁碳纳米角(o-SWNHs))的混合物发生水解和缩聚反应,合成了这种混合整体毛细管。与不含碳纳米颗粒的二氧化硅整体柱相比,所开发的整体毛细管柱对分析物表现出更高的萃取效率,这可归因于碳纳米颗粒的存在。在这方面,嵌入c-MWCNTs的二氧化硅整体柱表现出最佳性能。所得的整体毛细管还通过扫描电子显微镜(SEM)、元素分析和压汞法进行了表征。以多环芳烃(PAHs)为目标分析物,深入研究了影响吸附剂相制备的变量,包括三种不同的碳纳米颗粒和萃取参数。选择气相色谱-质谱联用作为仪器技术。检测限范围为0.1至0.3μg/L,萃取单元间的精密度(以相对标准偏差表示)在5.9%至14.4%之间。