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Fractionation methods differential

We also remark that Eq. (5.44) may be decomposed into separate sets of equations for the odd and even ap(t) which are decoupled from each other. Essentially similar differential recurrence relations for a variety of relaxation problems may be derived as described in Refs. 4, 36, and 73-76, where the frequency response and correlation times were determined exactly using scalar or matrix continued fraction methods. Our purpose now is to demonstrate how such differential recurrence relations may be used to calculate mean first passage times by referring to the particular case of Eq. (5.44). [Pg.387]

In the petroleum industry, the method of fractional distillation, differential distillation, or rectification is utilized for the primary separation of crude oil into fractions with regard to their boiling temperatures, because simple distillation is not efficient for separating liquids whose boiling points lie close to one another. [Pg.235]

DiFTerential settling methods. Differential settling methods utilize the difference in terminal velocities that can exist between substances of different density. The density of the medium is less than that of either substance. The disadvantage of the method is that since the mixture of materials to be separated covers a range of particle sizes, the larger, light particles settle at the same rate as the smaller, heavy ones and a mixed fraction is obtained. [Pg.1050]

For the solution of the fractional-order differential equations, most effective and easy analytic methods were developed based on the formula of the Laplace transform method of the Mittag-Leffler function in two parameters for further details see Refs. [19,38]. [Pg.384]

In order to identify compounds responsible for specific effects (i.e., endocrine disrupting or AhR hgands) observed in field studies, TIE or bioassay directed analysis approaches have increasingly been apphed over the last decade. In such approaches, sensitive bioassays are used to direct the fractionation of a sample extract until its complexity is sufficiently reduced to enable identification of those compoimds responsible for the activity measured in the bioassay. This strategy is based on differential extraction and fractionation methods and identification by chemical and biochemical analysis. TIE is a well-established technique having been originally developed by... [Pg.43]

A Simple Method for the Determination of Urinary 17-Ketogenic Steroid Fractions by Differential Solvent Extraction. I. Study of the Feasibility of Solvent Fractionation by Gas Chromatography Horumon to Rinsho 27(8) 903-908 (1979) CA 92 2788m... [Pg.119]

The method of obtaining and handling rat thoracic duct lymphocytes (TDL) has been detailed previously (1). The preparation of homogenates of rat TDL, fractionation by differential and isopycnic centrifugation, and calculations were carried out according to procedures described by Bowers (1), Beaufay (2), and Leighton... [Pg.301]

Differential centrifugation. Rat TDL are difficult cells to rupture under isotonic conditions, but it can be achieved if they are subjected to hypotonic shock (1) or treated with rabbit anti-rat lymphocyte antiserum and complement. Homogenates of rat TDL prepared by these two methods and fractionated by differential centrifugation... [Pg.301]

The SCB distribution (SCBD) has been extensively studied by fractionation based on compositional difference as well as molecular size. The analysis by cross fractionation, which involves stepwise separation of the molecules on the basis of composition and molecular size, has provided information of inter- and intramolecular SCBD in much detail. The temperature-rising elution fractionation (TREE) method, which separates polymer molecules according to their composition, has been used for HP LDPE it has been found that SCB composition is more or less uniform [24,25]. It can be observed from the appearance of only one melt endotherm peak in the analysis by differential scanning calorimetry (DSC) (Fig. 1) [26]. Wild et al. [27] reported that HP LDPE prepared by tubular reactor exhibits broader SCBD than that prepared by an autoclave reactor. The SCBD can also be varied by changing the polymerization conditions. From the cross fractionation of commercial HP LDPE samples, it has been found that low-MW species generally have more SCBs [13,24]. [Pg.278]

Spin trap, 102 Statistical kinetics, 76 Steady-state approximation, 77-82 Stiff differential equations, 114 Stoichiometric equations, 12 Stopped-flow method, 253-255 Substrate titration, 140 Success fraction approach, 79 Swain-Scott equation, 230-231... [Pg.281]

Third, the bulk of the items in Table 1 address method performance. These requirements must be satisfied on a substrate-by-substrate basis to address substrate-specific interferences. As discussed above, interferences are best dealt with by application of conventional sample preparation techniques use of blank substrate to account for background interferences is not permitted. The analyst must establish a limit of detection (LOD), the lowest standard concentration that yields a signal that can be differentiated from background, and an LOQ (the reader is referred to Brady for a discussion of different techniques used to determine the LOD for immunoassays). For example, analysis of a variety of corn fractions requires the generation of LOD and LOQ data for each fraction. Procedural recoveries must accompany each analytical set and be based on fresh fortification of substrate prior to extraction. Recovery samples serve to confirm that the extraction and cleanup procedures were conducted correctly for all samples in each set of analyses. Carrying control substrate through the analytical procedure is good practice if practicable. [Pg.722]


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