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Development linear

The exponent n = j3 + X, where j3 is the number of steps involved in nucleus formation (frequently j3 = 1 or 0, the latter corresponding to instantaneous nucleation) and X is the number of dimensions in which the nuclei grow (X = 3 for spheres or hemispheres, 2 for discs or cylinders and 1 for linear development). Most frequently, it is found that 2 < n < 4. Since n is a compound term, the value determined does not necessarily provide a unique measurement of both j3 and X. Ambiguity may arise where, for example, n = 3 could be a consequence of (j3 = 2, X = 1), (j3 = 1,... [Pg.57]

Single linear developments are mostly employed in the vertical mode. The apph-cabihty of the horizontal mode is discussed in Chapter 6. For circular and anticircular developments, the movement of the mobile phase is two-dimensional however, from the standpoint of sample separation it is a one-dimensional technique. Circular developments result in higher hRp values compared to linear ones imder the same conditions, and compoimds are better resolved in the lower-AR range. The same effect is noticed on plates with a layer thickness gradient (see Section 5.2.1). On the other hand, using antieircular developments, compounds are bettCT resolved in the upper-M range. [Pg.120]

Isocratic linear development is the most popular mode of chromatogram development in analytical and preparative planar chromatography. It can be easily performed in horizontal chambers of all types. The mobile phase in the reservoir is brought into contact with the adsorbent layer, and then the movement of the eluent front takes place. Chromatogram development is stopped when the mobile phase front reaches the desired position. Usually 20 X 20 cm and 10 X 20 cm plates are applied for preparative separations, and this makes the migration distance equal to about 18 cm. Due to the fact that the migration distance varies with time according to the equation Z, = (Z, c, and t are the distance of the solvent front traveled, constant,... [Pg.140]

Linear development is carried out in the ascending or horizontal mode in a saturated (lined with thick hlter paper) or unsaturated [8] rectangular chamber... [Pg.178]

The fundamental parimeter used to characterize the position of a saaple zone in a TLC chromatograa is the retardation factor, or Rf value. It represents the ratio of the distance migrated by the saaple compared to that traveled by the solvent front. With respect to Figure 7.1, the Rf value for linear development is given by equation (7.1)... [Pg.843]

Related to the linear development chamber is the Vario-KS chamber [8,195]. The plate is also developed in the horizontal position in a sandwich configuration. However, this chamber is... [Pg.873]

Liquid flows into a tank at the rate of Q m3/s. The tank has three vertical walls and one sloping outwards at an angle fi to the vertical. The base of the tank is a square with sides of length x m and the average operating level of liquid in the tank is Z0 m. If the relationship between liquid level and flow out of the tank at any instant is linear, develop an expression for the time constant of the system. [Pg.313]

The trial-by-fire methods of science, however, sidetracked the linear development of high polymer theory, for the theory was swept up by the development of the association theory of collodal particles at about the turn of the century. The peculiar and hard to understand chemical and physical behavior of polymers had, on occasions, lead to the suggestion that unusual or special forces were involved in their formation. In order to explain the forces, workers turned to the work of Thomas Graham. [Pg.28]

The time course of protein-polyphenol haze development in many packaged clear beverages has a two-phase pattern (see, for example, Fig. 2.17). At first no observable change occurs for some time. After this, haze formation begins and follows an essentially linear development rate. This phenomenon has been reported in beer (McMurrough et al., 1992) as well as apple juice, grape juice, and cranberry juice cocktail (Siebert, 1999, 2006). [Pg.73]

When comparing the above two methods to linear development, anticircular apparently is superior in terms of sensitivity, number of samples per plate, speed of analysis, and solvent consumption. Conventional linear TLC ranked second to the anticircular techniques [46], Also refer to the Handbook of Thin-Layer Chromatography [27] for additional details. [Pg.294]

We use the quadratic mixing rule for the covolume parameter in the MHV2 method, instead of the original linear development. This modification largely increases the performance, as can be noticed on table 4, when we compared the prediction of M3 and Ml7 methods, as well as M4 and Ml 8 methods ... [Pg.355]

Two-dimensional TLC can be usetiil when particular separations are needed. The plate is run in one direction with the first mobile phase, dried, turned throu 90°, and run again using a different mobile phase. This metiiod is better than linear development since all the plate is used for separating the components of a sample. However, only one sample can be sep ated on each plate. [Pg.163]

Fig.l Cassette of foil-backed layer for linear development 1 = cover sheet, 2 = sorbent layer, 3 = eluent puncture, 4 = eluent trough, 5 = sample application site. [Pg.1104]

In linear development of a chromatogram, unidirectional or bidirectional developments of the chromatogram are possible. Similarly, as in liquid column chromatography, there are possible, in this case, either on-line or off-line techniques of sample application, separation, and detection, as well as various modifications (e.g., partly off-line method). Bidirectional development can also be vertical. Using vertical bidimensional development, applying different eluents, components of complex, difficult mixtures can be separated. The separation of such mixtures is also possible by means of this technique using multiple automatic development of chromatogram. [Pg.1104]


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