Billen Jeroen, Broeckhoven Ken, Liekens Anuschka, Choikhet Konstantin, Rozing Gerard, Desmet Gert
Vrije Universiteit Brussel, Department of Chemical Engineering, Pleinlaan 2, 1050 Brussels, Belgium.
J Chromatogr A. 2008 Nov 7;1210(1):30-44. doi: 10.1016/j.chroma.2008.09.056. Epub 2008 Sep 20.
To fulfil the increasing demand for faster and more complex separations, modern HPLC separations are performed at ever higher pressures and temperatures. Under these operating conditions, it is no longer possible to safely assume the mobile phase fluid properties to be invariable of the governing pressures and temperatures, without this resulting in significantly deficient results. A detailed insight in the influence of pressure and temperature on the physico-chemical properties of the most commonly used liquid mobile phases: water-methanol and water-acetonitrile mixtures, therefore becomes very timely. Viscosity, isothermal compressibility and density were measured for pressures up to 1000 bar and temperatures up to 100 degrees C for the entire range of water-methanol and water-acetonitrile mixtures. The paper reports on two different viscosity values: apparent and real viscosities. The apparent viscosities represent the apparent flow resistance under high pressure referred to by the flow rates measured at atmospheric pressure. They are of great practical use, because the flow rates at atmospheric pressure are commonly stable and more easily measurable in a chromatographic setup. The real viscosities are those complying with the physical definition of viscosity and they are important from a fundamental point of view. By measuring the isothermal compressibility, the actual volumetric flow rates at elevated pressures and temperatures can be calculated. The viscosities corresponding to these flow rates are the real viscosities of the solvent under the given elevated pressure and temperature. The measurements agree very well with existing literature data, which mainly focus on pure water, methanol and acetonitrile and are only available for a limited range of temperatures and pressures. As a consequence, the physico-chemical properties reported on in this paper provide a significant extension to the range of data available, hereby providing useful data to practical as well as theoretical chromatographers investigating the limits of modern day HPLC.
为满足对更快、更复杂分离日益增长的需求,现代高效液相色谱(HPLC)分离在越来越高的压力和温度下进行。在这些操作条件下,如果不考虑流动相流体性质随压力和温度的变化,就无法安全地假定其不变,否则会导致明显不足的结果。因此,深入了解压力和温度对最常用的液体流动相(水 - 甲醇和水 - 乙腈混合物)物理化学性质的影响变得非常及时。对水 - 甲醇和水 - 乙腈混合物的整个范围,在高达1000巴的压力和高达100摄氏度的温度下测量了粘度、等温压缩率和密度。本文报道了两种不同的粘度值:表观粘度和真实粘度。表观粘度表示在高压下的表观流动阻力,由在大气压下测量的流速来表示。它们具有很大的实际用途,因为大气压下的流速通常稳定且在色谱装置中更容易测量。真实粘度符合粘度的物理定义,从基本观点来看很重要。通过测量等温压缩率,可以计算出高压和高温下的实际体积流速。与这些流速对应的粘度是给定高压和温度下溶剂的真实粘度。这些测量结果与现有文献数据非常吻合,现有文献数据主要集中在纯水、甲醇和乙腈,并且仅适用于有限的温度和压力范围。因此,本文报道的物理化学性质显著扩展了可用数据的范围,从而为研究现代HPLC极限的实际和理论色谱工作者提供了有用的数据。