Gross Gwen M, Prazen Bryan J, Grate Jay W, Synovec Robert E
Center for Process Analytical Chemistry, Department of Chemistry, Box 351700, University of Washington, Seattle, WA 98195, USA.
Anal Chem. 2004 Jul 1;76(13):3517-24. doi: 10.1021/ac049909g.
A novel injection technique for high-speed gas chromatography is demonstrated. Synchronized dual-valve injection is shown to provide peak widths as low as 1.5 ms (width at half-height) for an unretained analyte. This was achieved using a 0.5-m DB-5 column with an internal diameter of 100 microm and a film thickness of 0.4 microm operated at a temperature of 150 degrees C with a column absolute head pressure of 85 psi, resulting in a dead time of only t(o) = 26 ms ( approximately 1900 cm/s, 26 mL/min). Using the DB-5 column in a 1-m length under the same instrumental parameters, with a resulting linear flow velocity of 935 cm/s (12.7 mL/min, t(o) = 117 ms), a minimum peak width of 3.3 ms was obtained. During an isothermal separation, 10 analytes were separated in a time window of 400 ms. A rigorous comparison of experimental and theoretical band-broadening data based on the Golay equation showed that band broadening is limited almost entirely by the chromatographic band broadening terms expressed by the Golay equation and not by extra column band broadening due to the injection process. Synchronized dual-valve injection offers a rugged and inexpensive design, providing extremely reproducible injections with peak height precision of 2.4% (RSD) and low run-to-run variation in retention times, with an average standard deviation less than 0.1 ms. Herein, synchronized dual-valve injection is demonstrated as a proof of principle using high-speed diaphragm valves. It is foreseen that the injection technique could be readily implemented using a combination of thermal modulation and high-speed valve hardware, thus optimizing the mass transfer and not significantly sacrificing the limit of detection performance for high-speed GC. Further implications are that, if properly implemented, high-speed temperature programming coupled with this new technology should lead to very large peak capacities for approximately 1-s separations.
本文展示了一种用于高速气相色谱的新型进样技术。结果表明,同步双阀进样可使未保留分析物的峰宽低至1.5毫秒(半高宽)。这是通过使用一根0.5米长、内径100微米、膜厚0.4微米的DB - 5色谱柱实现的,该色谱柱在150℃温度下运行,柱绝对压头为85 psi,死时间仅为t(o)=26毫秒(约1900厘米/秒,26毫升/分钟)。在相同仪器参数下,使用1米长的DB - 5色谱柱,线性流速为935厘米/秒(12.7毫升/分钟,t(o)=117毫秒),获得的最小峰宽为3.3毫秒。在等温分离过程中,10种分析物在400毫秒的时间窗口内实现了分离。基于Golay方程对实验和理论谱带展宽数据进行的严格比较表明,谱带展宽几乎完全受Golay方程表示的色谱谱带展宽项限制,而非进样过程导致的柱外谱带展宽。同步双阀进样提供了一种坚固且廉价的设计,进样具有极高的重现性,峰高精密度为2.4%(相对标准偏差),保留时间的批间变化小,平均标准偏差小于0.1毫秒。本文使用高速隔膜阀展示了同步双阀进样作为原理验证。可以预见,结合热调制和高速阀硬件,该进样技术能够轻松实现,从而优化传质,且不会显著牺牲高速气相色谱检测性能的极限。进一步的意义在于,如果实施得当,高速程序升温与这项新技术相结合,对于大约1秒的分离应能实现非常大的峰容量。