Collin William R, Nuñovero Nicolas, Paul Dibyadeep, Kurabayashi Katsuo, Zellers Edward T
Department of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055, USA; Center for Wireless Integrated MicroSensing and Systems (WIMS(2)), University of Michigan, Ann Arbor, MI 48109-2122, USA.
Department of Environmental Health Sciences, University of Michigan, Ann Arbor, MI 48109-2029, USA; Center for Wireless Integrated MicroSensing and Systems (WIMS(2)), University of Michigan, Ann Arbor, MI 48109-2122, USA.
J Chromatogr A. 2016 Apr 29;1444:114-22. doi: 10.1016/j.chroma.2016.03.072. Epub 2016 Mar 26.
Comprehensive two-dimensional gas chromatography (GC×GC) with a temperature-programmed microfabricated thermal modulator (μTM) is demonstrated. The 0.78 cm(2), 2-stage μTM chip with integrated heaters and a PDMS coated microchannel was placed in thermal contact with a solid-state thermoelectric cooler and mounted on top of a bench scale GC. It was fluidically coupled through heated interconnects to an upstream first-dimension ((1)D) PDMS-coated capillary column and a downstream uncoated capillary or second-dimension ((2)D) PEG-coated capillary. A mixture of n-alkanes C6-C10 was separated isothermally and the full-width-at-half-maximum (fwhm) values of the modulated peaks were assessed as a function of the computer-controlled minimum and maximum stage temperatures of μTM, Tmin and Tmax, respectively. With Tmin and Tmax fixed at -25 and 100°C, respectively, modulated peaks of C6 and C7 had fwhm values<53 ms while the modulated peaks of C10 had a fwhm value of 1.3s, due to inefficient re-mobilization. With Tmin and Tmax fixed at 0 and 210°C, respectively, the fwhm value for the modulated C10 peaks decreased to 67 ms, but C6 and C7 exhibited massive breakthrough. By programming Tmin from -25 to 0°C and Tmax from 100 to 220°C, the C6 and C7 peaks had fwhm values≤50 ms, and the fwhm for C10 peaks remained<95 ms. Using the latter conditions for the GC×GC separation of a sample of unleaded gasoline yielded resolution similar to that reported with a commercial thermal modulator. Replacing the PDMS phase in the μTM with a trigonal-tricationic room temperature ionic liquid eliminated the bleed observed with the PDMS, but also reduced the capacity for several test compounds. Regardless, the demonstrated capability to independently temperature program this low resource μTM enhances its versatility and its promise for use in bench-scale GC×GC systems.
展示了配备程序升温微制造热调制器(μTM)的全二维气相色谱(GC×GC)。将具有集成加热器和涂有聚二甲基硅氧烷(PDMS)的微通道的0.78平方厘米两级μTM芯片与固态热电冷却器进行热接触,并安装在台式气相色谱仪顶部。它通过加热的互连管道与上游的一维((1)D)涂有PDMS的毛细管柱以及下游的未涂覆毛细管或二维((2)D)涂有聚乙二醇(PEG)的毛细管进行流体连接。对正己烷至正癸烷的混合物进行等温分离,并分别根据计算机控制的μTM最低和最高阶段温度Tmin和Tmax评估调制峰的半高宽(fwhm)值。当Tmin和Tmax分别固定在-25°C和100°C时,由于再迁移效率低下,正己烷和正庚烷的调制峰fwhm值<53毫秒,而正癸烷的调制峰fwhm值为1.3秒。当Tmin和Tmax分别固定在0°C和210°C时,调制的正癸烷峰的fwhm值降至67毫秒,但正己烷和正庚烷出现大量穿透。通过将Tmin从-25°C编程至0°C,Tmax从100°C编程至220°C,正己烷和正庚烷峰的fwhm值≤50毫秒,正癸烷峰的fwhm值保持<95毫秒。使用后一种条件对无铅汽油样品进行GC×GC分离,得到的分离度与使用商用热调制器报道的结果相似。用三角三阳离子室温离子液体替代μTM中的PDMS相消除了PDMS观察到的流失现象,但也降低了几种测试化合物的容量。无论如何,所展示的独立对这种低资源μTM进行温度编程的能力增强了其通用性以及在台式GC×GC系统中使用的前景。