Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Experimental separation

Due to difficulties and uncertainties in the experimental separation of the porous media [93], and the inevitability of approximations in the analytical treatment [87,89], the nature of the chain movement in a random environment is still far from being well understood, and theoretical predictions are controversial [87,89]. Thus, on the ground of replica calculations within a variational approach, one predicts three regimes [87] in which the chain gyration radius Rg scales with the number of repeatable units N as rI (X for low, R x N for medium, and R x for high... [Pg.600]

Mulliken, R.S. and Harkins, W.D. (1922). The separation of isotopes. Theory of resolution of isotopic mixtures by diffusion and similar processes. Experimental separation of mercury by evaporation in a vacuum. Journal of the American Chemical Society 44 37-65. [Pg.342]

The efficiency of the cyclone separator is greater for large than for small particles, and it increases with the throughput until the point is reached where excessive turbulence is created. Figure 1.55 shows the efficiency of collection plotted against particle size for an experimental separator for which the theoretical cut occurs at about 10 ttm. It may be noted that an appreciable quantity of fine material is collected, largely as a result of agglomeration, and that some of the coarse material is lost with the result that a sharp cut is not obtained. [Pg.78]

It becomes obvious from the clustered data points that the binding constant for the 7 -enantiomer is too small to be accurately determined by this method. Hence, indirect affinity CE (resolution method) was utilized to determine the binding constant for the 7 -enantiomer. Indirect affinity CE makes use of the knowledge of the constant for one enantiomer (here, A s) and in addition of experimental separation data as obtained with the racemate of DNB-Leu in presence of the tBuCQN selector as BGE additive. By use of Equation 1.10, an enantioselectivity factor may be defined as the ratio of the binding constants of S- and 7 -enantiomers yielding the following equation ... [Pg.40]

The challenge is therefore to develop an experiment which allows an experimental separation of the contributions from chain entangling and cross-links. The Two-Network method developed by Ferry and coworkers (17,18) is such a method. Cross-linking of a linear polymer in the strained state creates a composite network in which the original network from chain entangling and the network created by cross-linking in the strained state have different reference states. We have simplified the Two-Network method by using such conditions that no molecular theory is needed (1,21). [Pg.54]

Pool-Loading Experiments and Possibility that Reduction in Incorporation Reduces Influx into Soluble Pool. In order to empirically eliminate the possibility that the observed reduction in uptake of labelled amino acids into the soluble pool was an indirect result of an inhibition of incorporation, it was necessary to experimentally separate the influx and incorporation systems in vivo. The operational compromise required to accomplish this has been given by Sacher (55), and involves in the present case measuring the rates of label incorporation in control and treated tissues which have had their soluble pools fully loaded with unlabelled amino acid. Thus, the label-specific... [Pg.141]

Proof of the existence of a volatile pheromone is more straightforward, but experimental separation of olfactory from visual, vibrational, and acoustic cues remains essential. Mate location may be mediated by pheromones in many spider species, because spiders, like insects, often face the task of locating a mate at some distance. [Pg.120]

Theory suggests that ternary moments vary substantially with temperature even sign changes occur with modest temperature variations. This fact offers intriguing possibilities for an experimental separation of the pairwise-additive and the irreducible three-body effects and, perhaps, for a critical search for irreducible ternary contributions. [Pg.304]

Figure 19.12. Batch parametric processing of solid-liquid interactions such as adsorption or ion exchange. The bottom reservoir and the bed interstices are filled with the initial concentration before pumping is started, (a) Arrangement of adsorbent bed and upper and lower reservoirs for batch separation, (b) Synchronization of temperature levels and directions of flow (positive upward), (c) Experimental separation of a toluene and n-hcptane liquid mixture with silica gel adsorbent using a batch parametric pump. (Reprinted from Wilhelm, 1968, with permission of the American Chemical Society), (d) Effect of cycle time t on reservoir concentrations of a closed system for an NaCl-H20 solution with an ion retardation resin adsorbent. The column is initially at equilibrium with 0.05M NaCl at 25°C and a = 0.8. The system operates at 5° and 55°C. [Sweed and Gregory, AIChE J. 17, 171 (1971)J. Figure 19.12. Batch parametric processing of solid-liquid interactions such as adsorption or ion exchange. The bottom reservoir and the bed interstices are filled with the initial concentration before pumping is started, (a) Arrangement of adsorbent bed and upper and lower reservoirs for batch separation, (b) Synchronization of temperature levels and directions of flow (positive upward), (c) Experimental separation of a toluene and n-hcptane liquid mixture with silica gel adsorbent using a batch parametric pump. (Reprinted from Wilhelm, 1968, with permission of the American Chemical Society), (d) Effect of cycle time t on reservoir concentrations of a closed system for an NaCl-H20 solution with an ion retardation resin adsorbent. The column is initially at equilibrium with 0.05M NaCl at 25°C and a = 0.8. The system operates at 5° and 55°C. [Sweed and Gregory, AIChE J. 17, 171 (1971)J.
The evidence for isomerism varies from the obvious, such as a difference in phase, to the subtle, such as the temperature dependence of an NMR spectrum. These instances illustrate an important point, namely, that the detection of isomerism is dependent upon the existence of an energy barrier between the different forms and upon a method of detection sensitive enough to observe the barrier. A compound that appears to be a single species on one time-scale may prove to be a mixture on another. The relationship between the lifetime of a particular molecular structure and the various physical methods for studying it has been discussed by Muetterties.3 The essentially instantaneous method of X-ray diffraction (10 18s) may be contrasted with NMR techniques (10 1-10 9s) and the time scale for the experimental separation of isomers (>102s). [Pg.180]

Single particle energies (SPE s) are determined by fitting the experimental separation of the 7/2+. state from other excitation states. As corrections are made to a given two-body interaction SPE s are redetermined. [Pg.80]

The experimental separation of the 2F pair of levels in Ce3+ has been found by Lang [333] to be 2253 cm-1 which gives a free-ion value for the spin-orbit constant parameter of 644 cm-1. [Pg.707]

For the evaluation of the isotherm, Equation 1.119 should be used. Since there are several parameters (up to 7), the experimental separation of ion exchange and adsorption can be simpler (Chapter 2, Section 2.6). [Pg.63]

On the basis of those discussed here, we can say that the thermodynamic parameters of ion exchange determined by linear isotherm equations are not correct. We determine the mechanism of sorption (ion exchange and/or adsorption) and then choose the isotherm equation. When simultaneous interfacial processes take place, the dominant process, if any, has to be selected or experimentally separated, or Equation 1.119 should be used. [Pg.63]

The relatively slow reaction [40) is the reason why a polymer with various chain lengths is produced. New centres continue to be generated during the course of the polymerization with less and less monomer available. This difficulty is circumvented by experimental separation of initiation from propagation. A solution of oligomeric diions is added to the system prepared for polymerization. This technique requires special measures to prevent... [Pg.115]

Both experimental data and theoretical calculations show that the transition of a trigonal bipyramidal into a square pyramidal structure for compounds of penta-coordinate silicon does not require high energy consumption. Up to now the attempts of experimental separation of diastereomers of organosilicon compounds with penta-coordinate silicon atom were unsuccessful. For spirocyclic bisacetylaceto-nates, XYSi(Acac)2, containing a hexa-coordinate silicon atom, however, geometric isomerism has been observed... [Pg.117]

Table IV. Comparison of Experimental" Separation Factors of Various... Table IV. Comparison of Experimental" Separation Factors of Various...

See other pages where Experimental separation is mentioned: [Pg.495]    [Pg.357]    [Pg.11]    [Pg.183]    [Pg.135]    [Pg.289]    [Pg.542]    [Pg.149]    [Pg.216]    [Pg.96]    [Pg.36]    [Pg.302]    [Pg.48]    [Pg.374]    [Pg.44]    [Pg.35]    [Pg.36]    [Pg.443]    [Pg.416]    [Pg.280]    [Pg.432]    [Pg.32]    [Pg.640]    [Pg.642]    [Pg.110]    [Pg.158]    [Pg.182]    [Pg.113]    [Pg.387]    [Pg.257]    [Pg.230]    [Pg.73]    [Pg.86]   
See also in sourсe #XX -- [ Pg.429 ]




SEARCH



Chemical separation methods experimental techniques

Development of experimental methods for determining the phase separation region, critical point, spinodal and interaction parameter

Experimental Examples of Separations

Experimental Separation and Identification of Isomers

Separation, solid-liquid experimental selection routine

Singlet-triplet separation experimental determination

© 2024 chempedia.info