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Separators selection

Each separate selection of objects that is possible irrespective of the order in which they are arranged is called a combination. The number of combinations of n things taken r at a time, written C n, r) = n /... [Pg.432]

Equation (16-168) shows that the resolution is the result of independent effects of the separation selectivity (ot), column efficiency [Np), and capacity (k ). Generally, peaks are essentially completely resolved when R, = 1.5 (>99.5 percent separation). In practice, values of R, 1, corresponding to 98 percent separation, are often considered adequate. [Pg.1533]

From the system operadng pressure, establish the pressure rating designadon for the separator selection. [Pg.258]

Sizing, 451, 453, 455, 459, 462 Sonic flow, 461 Types, illustrations, 411-421 Rupture disk, liquids, 462, 466 Rupture disk/pressure-relief valves combination, 463 Safely relief valve, 400 See Relief valve Safety valve, 400, 434 Safety, vacuum, 343 Scale-up, mixing, 312, 314—316 Design procedure, 316-318 Schedules/summaries Equipment, 30, 31 Lines, 23, 24 Screen particle size, 225 Scrubber, spray, 269, 270 Impingement, 269, 272 Separator applications, liquid particles, 235 Liquid particles, 235 Separator selection, 224, 225 Comparison chart, 230 Efficiency, 231... [Pg.630]

The recovery of petroleum from sandstone and the release of kerogen from oil shale and tar sands both depend strongly on the microstmcture and surface properties of these porous media. The interfacial properties of complex liquid agents—mixtures of polymers and surfactants—are critical to viscosity control in tertiary oil recovery and to the comminution of minerals and coal. The corrosion and wear of mechanical parts are influenced by the composition and stmcture of metal surfaces, as well as by the interaction of lubricants with these surfaces. Microstmcture and surface properties are vitally important to both the performance of electrodes in electrochemical processes and the effectiveness of catalysts. Advances in synthetic chemistry are opening the door to the design of zeolites and layered compounds with tightly specified properties to provide the desired catalytic activity and separation selectivity. [Pg.169]

It is the main aim of semiempirical chromatographic models to couple the empirical parameters of retention with the established thermodynamic quantities generally used in physical chemistry. The validity of a model for chromatographic practice can hardly be overestimated, because it often and successfully helps to overcome the old trial-and-error approach to running the analyses, especially when incorporated in the separation selectivity oriented optimization strategy. [Pg.17]

Optimization of the chromatographic process by Snyder s concept of solvent polarity and selectivity is in fact the optimization of the separation selectivity that... [Pg.80]

Prus and Kowalska [75] dealt with the optimization of separation quality in adsorption TLC with binary mobile phases of alcohol and hydrocarbons. They used the window diagrams to show the relationships between separation selectivity a and the mobile phase eomposition (volume fraction Xj of 2-propanol) that were caleulated on the basis of equations derived using Soezewiriski and Kowalska approaehes for three solute pairs. At the same time, they eompared the efficiency of the three different approaehes for the optimization of separation selectivity in reversed-phase TLC systems, using RP-2 stationary phase and methanol and water as the binary mobile phase. The window diagrams were performed presenting plots of a vs. volume fraetion Xj derived from the retention models of Snyder, Schoen-makers, and Kowalska [76]. [Pg.93]

The popularity of reversed-phase liquid chromatography (RPC) is easily explained by its unmatched simplicity, versatility and scope [15,22,50,52,71,149,288-290]. Neutral and ionic solutes can be separated simultaneously and the rapid equilibration of the stationary phase with changes in mobile phase composition allows gradient elution techniques to be used routinely. Secondary chemical equilibria, such as ion suppression, ion-pair formation, metal complexatlon, and micelle formation are easily exploited in RPC to optimize separation selectivity and to augment changes availaple from varying the mobile phase solvent composition. Retention in RPC, at least in the accepted ideal sense, occurs by non-specific hydrophobic interactions of the solute with the... [Pg.202]

Hu, W. Z., Haddad, P. R., Tanakar, K., and Hasebe, K., Modulation of the separation selectivity of inorganic anions in electrostatic ion chromatography using acidic eluents, Analyst, 125, 241, 2000. [Pg.304]

Breadmore, M. C., Macka, M., and Haddad, P. R., Manipulation of separation selectivity for alkali metals and ammonium in ion-exchange capillary electrochromatography using a suspension of cation exchange particles in the electrolyte as a pseudo stationary phase, Electrophoresis, 20, 1987, 1999. [Pg.304]

Krokhin, O. V., Adamov, A. V., Hoshino, H., Shpigun, O. A., and Yotsuyanagi, T. Separation selectivity of some ethylenediaminetetraacetic acid and cyclohexane-1,2,-diaminetetraacetic acid complexes in column and ion electroki-netic chromatography, /. Chromatogr. A, 850, 269, 1999. [Pg.304]

Table 7.40 summarises the general characteristics of on-line SFC-MS. The method is potentially most useful for thermally labile and involatile compounds that are unsuitable for GC-MS. Because the MS instrument is the main source of information, the reproducibility of the retention and the separation selectivity are much less important than for other SFC applications. As a result, mass spectroscopists do not feel restrained by the limits on reproducibility, which slowed the uptake of SFC by chromatographers. Method development should not be underestimated. Practical problems are associated with interfacing and the effect of the expanding... [Pg.482]

If we consider only a few of the general requirements for the ideal polymer/additive analysis techniques (e.g. no matrix interferences, quantitative), then it is obvious that the choice is much restricted. Elements of the ideal method might include LD and MS, with reference to CRMs. Laser desorption and REMPI-MS are moving closest to direct selective sampling tandem mass spectrometry is supreme in identification. Direct-probe MS may yield accurate masses and concentrations of the components contained in the polymeric material. Selective sample preparation, efficient separation, selective detection, mass spectrometry and chemometric deconvolution techniques are complementary rather than competitive techniques. For elemental analysis, LA-ICP-ToFMS scores high. [Pg.744]

TABLE 12.1 Chromatographic Modes and Conditions Used for LC-MS Study of Tryptic Peptides Separation Selectivity... [Pg.266]

Separation selectivity in LC depends on various factors. The most important is the choice of the stationary and mobile phases (Chen et al., 2004 Guo et al., 1987). In addition, the separation temperature (Hancock et al., 1994) and gradient slope (Chloupek et al., 1994) have also been shown to have a moderate impact on LC selectivity. [Pg.266]

Reijenga JC, Gagliardi LG, Kenndler E. Temperature dependence of acidity constants, a tool to affect separation selectivity in capillary electrophoresis. J. Chromatogr.A 2007 1155 142-145. [Pg.285]


See other pages where Separators selection is mentioned: [Pg.429]    [Pg.444]    [Pg.451]    [Pg.367]    [Pg.55]    [Pg.31]    [Pg.1750]    [Pg.1751]    [Pg.98]    [Pg.224]    [Pg.642]    [Pg.224]    [Pg.146]    [Pg.92]    [Pg.221]    [Pg.430]    [Pg.234]    [Pg.235]    [Pg.236]    [Pg.236]    [Pg.263]    [Pg.429]    [Pg.545]    [Pg.727]    [Pg.267]    [Pg.267]    [Pg.268]    [Pg.307]    [Pg.308]   
See also in sourсe #XX -- [ Pg.224 , Pg.225 ]




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Alkali metal ions selective separation

Capillary electrochromatography separation buffer selection

Case Study Selection Guidelines for the Separation and Recovery of Hydrogen in Refineries

Chemical separation Selectivity

Criteria for Selection of Separation Methods

Elution separation selection

Equipment separation, selecting

Example 4-1 Basic Separator Type Selection

Gradient selection preparative separation

High selectivity, enantiomer separations

Improving Separation by Changing the Selectivity

Ionic Liquids, Catalyst Recycle, Selectivity, and Product Separation

Liquid-solid separators selection

Material selection separations

Membrane Gas Separation Selectivity a and the Pressure Ratio

Membrane separation perm-selectivity

Membrane separation selectivity

Polymer HPLC separation selectivity

Preliminary Separator Selection

Procedures for selected chromatographic separations

Pyrite selective flocculation, separation

Selected tests and separations

Selection Guidelines for Gas Separation

Selection of Cell-Separation Unit Operation

Selection of Pore Size and Separation Range

Selection of Separation and Detection Systems

Selection of Solvents for Other Separation Processes

Selection of a separation process

Selection of an Ion-Exchange-Reversed-Phase Separation System for Protein-Level Separations

Selection of the separation mode

Selective Guest Adsorption and Separation

Selective separating processes

Selective separation

Selectivity normal paraffin separation

Selectivity of Plasma-Treated Gas-Separating Polymer Membranes

Selectivity of separation

Selectivity separable kinetics

Selectivity separation

Selectivity separation

Selectivity, separation and

Separate solution method, selectivity

Separation (or selectivity) factor between two solutes

Separation Mechanism and Control of Selectivity

Separation Using Selective Dissolution

Separation equipment selection

Separation flowsheet synthesis selection

Separation of Xylenes Isomers by Selective Adsorption on FAU Type Zeolite

Separation processes selection

Separation selection criteria

Separation selective resins

Separation selectivity chromatography

Separation selectivity expression

Separation selectivity improving

Separation selectivity length

Separation selectivity methylene

Separation selectivity optimization

Separation selectivity testing

Separation selectivity tuning

Separation selectivity variations

Separation selectivity with chiral mobile-phase additives

Separation selectivity, displacement

Separation selectivity, displacement chromatography

Separation selectivity, solvent extraction

Separation technologies/processes selectivity improvement

Separation, energy requirement selection

Separation, solid-liquid experimental selection routine

Separator selection Efficiency

Single-line capacities for selected separation processes

Size exclusion chromatography separation selectivity

Size-selective separation

Solid-liquid, suspension separation, equipment selection

Solid/liquid separation equipment selection

Solid/liquid separation equipment, selection Software

Solid/liquid separation equipment, selection expert system

Solid/liquid separation equipment, selection methods

Solid/liquid separation filter media selection

The Separation Ratio (Selectivity) of a Solute

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