Effect of solvent strength and temperature on retention for a polar-endcapped, octadecylsiloxane-bonded silica stationary phase with methanol–water mobile phases

2004 ◽  
Vol 1060 (1-2) ◽  
pp. 177-185 ◽  
Author(s):  
W KIRIDENA ◽  
C POOLE ◽  
W KOZIOL
2003 ◽  
Vol 68 (1) ◽  
pp. 57-64 ◽  
Author(s):  
Marijana Acanski ◽  
Suzana Jovanovic-Santa ◽  
Lidija Jevric

The retention behavior and separation ability of a series of new 16,17-secoestrone derivatives has been studied on silica gel, alumina and C-18 silica gel layers with non-aqueous and aqueous-organic mobile phases. The retention behavior and separation ability are discussed in terms of the nature of the solute, eluent and stationary phase.


Author(s):  
Eldred H. Chimowitz

In this chapter, we discuss adsorption phenomena in supercritical systems, a situation that occurs in many application areas in chemical-process and materials engineering. An example of a commercial application in this area, which has achieved wide acceptance as a tool in analytical chemistry, is supercritical fluid chromatography (SFC). Not only is SFC a powerful technique for chemical analysis, but it also is a useful method for measuring transportive and thermodynamic properties in the near-critical systems. In the next section, we analyze adsorption-column dynamics using simple dynamic models, and describe how data from a chromatographic column can be used to estimate various thermodynamic and transport properties.We then proceed to discuss the effects of proximity to the critical point on adsorption behavior in these systems. The closer the system is to its critical point, the more interesting is its behavior. For very dilute solute systems, like those considered here, the energy balance is often ignored to a first approximation; this leads to a simple set of mass-balance equations defining transport for each species. These equations can be developed to various levels of complexity, depending upon the treatment of the adsorbent (stationary phase). The conceptual view of these phases can span a wide range of possibilities ranging from completely nonporous solids (fused structures) to porous materials with complicated ill-defined pore structures. Given these considerations, it is customary to make the following assumptions in the development of a simple model of adsorber-bed dynamics: . . .1. The stationary and mobile phases are continuous in the direction of the flow, with the fluid phase possessing a flat velocity profile (“plug” flow).. . . . . . 2. The porosity of the stationary phase is considered constant irrespective of pressure and temperature conditions (i.e., it is incompressible). . . . . . .3. The column is considered to be radially homogeneous, leading to a set of equations with one spatially independent variable, representing distance along the column axis. . . . . . . 4. The dispersion term in the model equation represents the combined effects of molecular diffusion and dispersion due to convective stirring in the bed. These effects are combined into an effective phenomenological dispersion coefficient, considered to be constant throughout the column. . . .


2011 ◽  
Vol 17 (4) ◽  
pp. 535-542 ◽  
Author(s):  
Marijana Acanski ◽  
Djura Vujuc ◽  
Suzana Jovanovic-Santa

The separation ability and retention of normal and reversed phase HPLC with, respectively, three non-polar and two polar mobile phases, have been studied by measuring the retention constants of a series of newly synthesized estrone derivatives. The separation ability and retention are discussed in terms of the nature of the solute, eluent and stationary phase. Good correlation was found between the retention constants log k0 of newly synthesized estrone derivatives obtained on C-18 column and log P calculated by different methods.


2009 ◽  
Vol 1216 (44) ◽  
pp. 7450-7455 ◽  
Author(s):  
Katina S.S. Dossou ◽  
Patrice Chiap ◽  
Bezhan Chankvetadze ◽  
Anne-Catherine Servais ◽  
Marianne Fillet ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Anna W. Sobanska ◽  
Jaroslaw Pyzowski

Ethylhexyl triazone (ET) was separated from other sunscreens such as avobenzone, octocrylene, octyl methoxycinnamate, and diethylamino hydroxybenzoyl hexyl benzoate and from parabens by normal-phase HPTLC on silica gel 60 as stationary phase. Two mobile phases were particularly effective: (A) cyclohexane-diethyl ether 1 : 1 (v/v) and (B) cyclohexane-diethyl ether-acetone 15 : 1 : 2 (v/v/v) since apart from ET analysis they facilitated separation and quantification of other sunscreens present in the formulations. Densitometric scanning was performed at 300 nm. Calibration curves for ET were nonlinear (second-degree polynomials), withR> 0.998. For both mobile phases limits of detection (LOD) were 0.03 and limits of quantification (LOQ) 0.1 μg spot−1. Both methods were validated.


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