ABSTRACT

Lilach Yishai-Aviram and Eli Grushka Department of Inorganic and Analytical Chemistry, The Hebrew University, Jerusalem, Israel

I. INTRODUCTION 274

II. THE PRINCIPLE OF DYNAMIC COATING 276

III. COLUMN CHARACTERIZATION 279

IV. POSITIVELY CHARGED POLYELECTROLYTES

AS STATIONARY PHASES 282

A. Coating Procedures 282

B. Properties of the Phases and Retention

Mechanism 284

C. Applications 289

V. NEGATIVELY CHARGED POLYELECTROLYTES

AS STATIONARY PHASES 289

A. Coating Procedures 289

B. Properties of the Phases and Retention

Mechanism 291

C. Applications 297

VI. COMPLEX POLYELECTROLYTE LAYERING 298

REFERENCES 298

Chemicallymodified silicas are used ubiquitously as stationary phase

support in liquid chromatography (LC). In spite of alternative column

packing, such as zirconia, alumina, titania, etc., silica continues to be

the most commonly used packing material in modern LC. The main

advantages of silica are its high level of mechanical strength, uni-

formity in terms of size and surface area, and purity. These qualities

permit the formation of efficient packed beds that remain stable under

high operating pressures for long periods of time [1]. The surface of

silica consists of various kinds of silanols and siloxane bonds [2,3].

The siloxane (Si-O-Si) sites are hydrophobic and contribute little or

nothing to the retention of polar solutes. However, the hydrophobic

nature of the siloxane bond makes it possible to observe some

retention of nonpolar solutes [4]. On the other hand, the silanol

groups, which can be hydrated by adsorption of water, are polar

and are considered to provide strong adsorption sites [3,5,6]. Basic

analytes can interact strongly with the acidic silanols.