Stationary phases solid

When the solid phase 0+ at x = -f oo coexists with the gas phase 0 at X = -oo, the stationary profile of the phase field is determined so as to minimize the free energy functional F (56). The functional derivative gives... 

Although solid-phase microextraction (SPME) has only been introduced comparatively recently (134), it has already generated much interest and popularity. SPME is based on the equilibrium between an aqueous sample and a stationary phase coated on a fibre that is mounted in a syringe-like protective holder. Eor extraction, the fibre... 

The packed-bed reactors discussed in Chapters 9 and 10 are multiphase reactors, but the solid phase is stationary, and convective flow occurs only through the fluid phase. The reaction kinetics are pseudohomogeneous, and components balances are written only for the fluid phase. 

Chapter 11 treats reactors where mass and component balances are needed for at least two phases and where there is interphase mass transfer. Most examples have two fluid phases, typically gas-liquid. Reaction is usually confined to one phase, although the general formulation allows reaction in any phase. A third phase, when present, is usually solid and usually catalytic. The solid phase may be either mobile or stationary. Some example systems are shown in Table 11.1. 

Many investigators have studied diffusion in systems composed of a stationary porous solid phase and a continuous fluid phase in which the solute diffuses. The effective transport coefficients in porous media have often been estimated using the following expression ... 

Five synthetic and five natural colorants were identified and quantified in lyo-philized dairy products and fatty foods using an automatic method based on solid phase extraction using a stationary phase followed by RP-HPLC C,g columns for the sequential retention of colorants and diode array detection. Lyophilization of the samples coupled with the separation procedure provided clean extracts despite the complexity of the food matrices and preserved the sample for at least 2 months without changes in colorant concentrations. The detection limits achieved for the colorants were found in a wide range from 0.03 to 75 pg/g of the lyophilized sample, according to the limits established by the European Union. ... 

Solid Phase or Adsorbents and Selection of the Stationary Phase... 

Ion-exchange solid-phase extractions are used for ionic compounds. The pH of the extracts is adjusted to ionize the target analytes so that they are preferentially retained by the stationary bonded phase. Selection of the bonded phase depends on the pK or pA b of the target analytes. Sample cleanup using ion exchange is highly selective and can separate polar ionic compounds that are difficult to extract by the liquid-liquid partition technique. 

Principles and Characteristics Solid-phase microextraction (SPME) is a patented microscale adsorp-tion/desorption technique developed by Pawliszyn et al. [525-531], which represents a recent development in sample preparation and sample concentration. In SPME analytes partition from a sample into a polymeric stationary phase that is thin-coated on a fused-silica rod (typically 1 cm x 100 p,m). Several configurations of SPME have been proposed including fibre, tubing, stirrer/fan, etc. SPME was introduced as a solvent-free sample preparation technique for GC. 

Selection of columns and mobile phases is determined after consideration of the chemistry of the analytes. In HPLC, the mobile phase is a liquid, while the stationary phase can be a solid or a liquid immobilised on a solid. A stationary phase may have chemical functional groups or compounds physically or chemically bonded to its surface. Resolution and efficiency of HPLC are closely associated with the active surface area of the materials used as stationary phase. Generally, the efficiency of a column increases with decreasing particle size, but back-pressure and mobile phase viscosity increase simultaneously. Selection of the stationary phase material is generally not difficult when the retention mechanism of the intended separation is understood. The fundamental behaviour of stationary phase materials is related to their solubility-interaction... 

In gc there is only one phase (the stationary liquid or solid phase) that is available for interaction with the sample molecules. Because the mobile phase is a gas, all sample vapours are soluble in it in all proportions. In hplc both the stationary phase and the mobile phase can interact selectively with the sample. Interactions such as complexation or hydrogen bonding that are absent in the gc mobile phase may occur in the hplc mobile phase. The variety of these selective interactions can also be increased by suitable chemical modification of the silica surface, hence hplc is a more versatile technique than gc, and can often achieve more difficult separations. 

The term three-phase fluidization, in this chapter, is taken as a system consisting of a gas, liquid, and solid phase, wherein the solid phase is in a non-stationary state, and includes three-phase slurry bubble columns, three-phase fluidized beds, and three-phase flotation columns, but excludes three-phase fixed bed systems. The individual phases in three-phase fluidization systems can be reactants, products, catalysts, or inert. For example, in the hydrotreating of light gas oils, the solid phase is catalyst, and the liquid and gas phases are either reactants or products in the bleaching of paper pulp, the solid phase is both reactant and product, and the gas phase is a reactant while the liquid phase is inert in anaerobic fermentation, the gas phase results from the biological activity, the liquid phase is product, and the solid is either a biological carrier or the microorganism itself. 

Separation of mixtures in microgram quantities by passage of the vaporized sample in a gas stream through a column containing a stationary liquid or solid phase components migrate at different rates due to differences in boiling point, solubility or adsorption. 

Preparative chromatographic processes are of increasing importance particularly in the production of fine chemicals. A mixture of compounds is introduced into the liquid mobile phase, and this then flows through a packed column containing the stationary solid phase. The contacting scheme is thus differential, but since the adsorption characteristics of the compounds in the mixture are similar, many equivalent theoretical stages are required for their separation. Chromatographic processes are mostly ran under transient conditions, such that... 

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