Gerard Rozing

Capillary electrochromatography — a high-efficiency micro-separation technique

Abstract Capillary electrochromatography (CEC) is a novel separation technique in which mobile phase transport through a capillary (50–200 μm I.D.) packed with stationary phase particles is achieved by electroosmotic flow (EOF) instead of a pressure gradient as in HPLC. Electroosmotic flow allows the usage of smaller particles and longer columns than in HPLC because of the absence of backpressure. Separation is achieved by partitioning between mobile and stationary phase and—in the case of charged analytes—by differential electrophoretic mobilities. In the reversed-phase mode, capillary electrochromatography has the potential to yield efficiencies five to ten times higher than standard RP-HPLC. For this reason CEC has started to create high interest among chromatographers. This paper will discuss the theoretical background of CEC, demonstrate the feasibility of CEC as a high-efficiency reversed-phase separation technique, compare theoretically achievable results to those obtained in practice and present fundamental studies on operational parameters such as dependence of EOF and efficiency on pH and organic modifier content.

Enantioseparations by electrochromatography with packed capillaries

Abstract ( S )-Naproxen-derived and (3 R ,4 S )-Whelk-O chiral stationary phases (CSPs) were immobilized on 3 μm silica supports and packed into 100 μm I.D. fused-silica capillaries. Enantiomers of some neutral analytes representing a variety of different classes of compounds were separated by electrochromatography using 2-(N-morpholino)ethanesulfonic acid modified with acetonitrile as the buffer system. High column efficiency (up to 200 000 plates per meter) and substantial levels of enantioselectivity were obtained in all cases with separations usually being performed in less than 10 min.

Separation of basic solutes by reversed-phase capillary electrochromatography.

The separation of basic solutes at low pH by capillary electrochromatography (CEC) has been investigated. The feasibility of separation of basic solutes by CEC was demonstrated. Influence of operational parameters, solvent composition, pH, temperature on retention and selectivity of the separation of a mixture of basic, neutral and acidic drug standards has been investigated. The observed elution behavior has been modeled to account for both chromatographic retention and differential electrophoretic mobility of the solutes. This model was verified experimentally. It is demonstrated in this work that the elution window of solutes in reversed-phase CEC is expanded to range from -1 to infinity.

Recent applications of capillary electrochromatography.

A review is presented of the most important recent applications of capillary electrochromatography (CEC) for the analysis of acidic, basic, and neutral compounds, of biomolecules, environmental substances, natural products, pharmaceuticals, and chiral compounds. Packed‐column CEC (packed‐CEC), open‐tubular (OT‐CEC), as well as pressure‐assisted CEC (pseudo‐CEC) are hereby considered. Papers published between July 1999 and April 2001 were taken into account. Applications before July 1999 have been reviewed in Electrophoresis 1999, 20, 3027 135 135–3065.

Towards the column bed stabilization of columns in capillary electroendosmotic chromatography. Immobilization of microparticulate silica columns to a continuous bed.

This article discusses a novel method generating a continuous bed inside the CEC column. The column bed composed of microparticulate reversed-phase silica is completely immobilized by a hydrothermal treatment using water for the immobilization process. This process eliminates the manufacture of frits of both ends of the column and all problems associated with their preparation. Fundamental studies on operational parameters will be presented such as the dependence of the immobilization on the column temperature, the type of stationary phase and the column back pressure. The immobilized CEC columns show the same high column efficiency as packed columns with frits.

Determination of band-spreading effects in high-performance liquid chromatographic instruments☆

Abstract The fundamentals of the measurement and computation of band spreading generated in chromatographic systems are discussed. A computer program was written that allows the characterization of the dispersion effects by calculating the second statistical moment of the concentration profiles emerging from the system. Experimental determination is necessary, as the existing theoretical models give quantitatively accurate values only in certain instances. In this way the dispersion contributions of various system elements were determined and useful hints for their design were obtained.

Influence of pressure and temperature on the physico-chemical properties of mobile phase mixtures commonly used in high-performance liquid chromatography

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.

Separation Efficiency of Particle-Packed HPLC Microchips

We report an experimental study of separation efficiency in microchip high-performance liquid chromatography (HPLC). For this study, prototype HPLC microchips were developed that are characterized by minimal dead volume, a separation channel with trapezoidal cross section, and on-chip UV detection. A custom-built stainless steel holder enabled microchip packing under pressures of up to 400 bar and ultrasonication. Bed densities were investigated with respect to the packing conditions and consistently related to pressure drop over the packed microchannels and separation efficiency under isocratic elution conditions. The derived plate height curves show a decrease of mobile phase mass transfer resistance with increasing bed density. High bed densities are critical to separation performance in noncylindrical packed beds, because only at low bed porosities does hydrodynamic dispersion in noncylindrical packings come close to that of cylindrical packings. At higher bed porosities, the presence of fluid channels of advanced flow velocity in the corners of noncylindrical packings affects hydrodynamic dispersion strongly. We demonstrate that the separation channels of HPLC microchips can be packed as densely as the cylindrical fused-silica capillaries used in nano-HPLC and that consequently microchip-HPLC separation efficiencies comparable to those of nano-HPLC can be achieved.

Packing density, permeability, and separation efficiency of packed microchips at different particle-aspect ratios.

HPLC microchips are investigated experimentally with respect to packing density, pressure drop-flow rate relation, hydraulic permeability, and separation efficiency. The prototype microchips provide minimal dead volume, on-chip UV detection, and a 75 mm long separation channel with a ca. 50 microm x 75 microm trapezoidal cross-section. A custom-built stainless-steel holder allowed to adopt optimized packing conditions. Separation channels were slurry-packed with 3, 5, and 10 microm-sized spherical, porous C8-silica particles. Differences in interparticle porosity, permeability, and plate height data are analyzed and consistently explained by different microchannel-to-particle size (particle-aspect) ratios and particle size distributions.

High temperature and temperature programming in capillary electrochromatography.

In electrochromatography, solvent electrophoretic mobility and solute partitioning are temperature dependent processes. If temperature variations are controlled, solute selectivity and analysis times can be tailored. In this study the feasibility of temperature programming in capillary electrochromatography (CEC) was demonstrated using a reversed-phase CEC mode. The outcome of programmed separations was compared with isothermal, isocratic and isorheic (constant flow) separations. The combined effects of column temperature and mobile phase flow-rate changes during the separation run, resulted in up to a 50% reduction in the separation run time, without adversely affecting the quality of separation. For capillary electrochromatography, temperature programming may be a valuable alternative to solvent programming modes because of the great technical difficulties associated with carrying out solvent gradient elution.