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Stability variation

Density Gradient Stabilization Variation of the PVP concentration gradient... [Pg.133]

The instability arises and evolves owing to thermodynamic fluctua tion (3.29). Such a fluctuation may cause complete system state decay (see, e.g., region V of unstable saddles in Figure 3.4). Flowever, it may also happen that the arising instability creates a new state of the system to be stabilized in time and space. An example is the formation of the limit (restricted) cycle in a system that involves the exceptional point of the unstable focus type. The orbital stability of such a system means exactly the existence of certain time stabilized variations in the thermody namic parameters (for example, the concentrations of reactants) that are... [Pg.157]

Cho et al. [280] compared dc and rf gas jet-boosted GD-AES for the analysis of steel in terms of the voltage-current relationship they studied the effects of the gas flow-rate (0-800 ml/min) and pressure (3-5 torr) on the dc bias potential, sample weight loss and emission intensity. The use of a simultaneous spectrometer for the rf mode proved dispensable by virtue of the high stability (variations less than 0.3%) for both matrix and trace elements. Both the rf and the dc mode provided calibration graphs that were linear over two or three decades (or even more if the analytical signal was normalized to the signal of a matrix component) however, the limits of detection obtained in the rf mode for many trace elements in steel were at the level of tens of ppb, which was an order of magnitude better than in the dc mode. [Pg.423]

The development of turbidity of AgCl is a rather slow process. A time lapse of 15-20 min after the addition of silver nitrate is necessary to allow the AgCl precipitate to become stabilized. Variations of temperature within the range 20-30°C, and of acidity between 0.01 and 0. IM HNO3 have no effect on the determination. [Pg.154]

The static stability of a foam refers to the ability of the foam to resist bubble breakdown. The foam s static stability can be quantified by measuring its half-life. This is the time required at static conditions for the foam to drain half of its liquid volume. As parameters such as type of stabilizer, containment pressure, or foam generation process change, the stability will also change. Foam half-life is not a direct measurement of stability. Variations of foam stability will occur under different conditions. [Pg.357]

Figure 10.2. Conditions for pore stability variation of dihedral angle for pore stability with the number of grains surrounding a pore/... Figure 10.2. Conditions for pore stability variation of dihedral angle for pore stability with the number of grains surrounding a pore/...
The remarkable stability and eontrollability of NMR speetrometers penults not only the preeise aeeiimulation of FIDs over several hours, but also the aequisition of long series of speetra differing only in some stepped variable sueh as an interpulse delay. A peak at any one ehemieal shift will typieally vary in intensity as this series is traversed. All the sinusoidal eomponents of this variation with time ean then be extraeted, by Fourier transfomiation of the variations. For example, suppose that the nomial ID NMR aequisition sequenee (relaxation delay, 90° pulse, eolleet FID) is replaeed by the 2D sequenee (relaxation delay, 90° pulse, delay i -90° pulse, eolleet FID) and that x is inereased linearly from a low value to ereate the seeond dimension. The polarization transfer proeess outlined in die previous seetion will then eause the peaks of one multiplet to be modulated in intensity, at the frequeneies of any other multiplet with whieh it shares a eoupling. [Pg.1457]

Disadvantages. The magic angle must be extremely stable and accurately set. The spiiming speed must show good stability over the duration of the experiment. The probe needs to be accurately tuned and careful correction for irradiation and detection variations with frequency, and baseline effects are necessary. The gain... [Pg.1485]

An even coarser description is attempted in Ginzburg-Landau-type models. These continuum models describe the system configuration in temis of one or several, continuous order parameter fields. These fields are thought to describe the spatial variation of the composition. Similar to spin models, the amphiphilic properties are incorporated into the Flamiltonian by construction. The Flamiltonians are motivated by fiindamental synnnetry and stability criteria and offer a unified view on the general features of self-assembly. The universal, generic behaviour—tlie possible morphologies and effects of fluctuations, for instance—rather than the description of a specific material is the subject of these models. [Pg.2380]

A combination of equation (C2.6.13), equation (C2.6.14), equation (C2.6.15), equation (C2.6.16), equation (C2.6.17), equation (C2.6.18) and equation (C2.6.19) tlien allows us to estimate how low the electrolyte concentration needs to be to provide kinetic stability for a desired lengtli of time. This tlieory successfully accounts for a number of observations on slowly aggregating systems, but two discrepancies are found (see, for instance, [33]). First, tire observed dependence of stability ratio on salt concentration tends to be much weaker tlian predicted. Second, tire variation of tire stability ratio witli particle size is not reproduced experimentally. Recently, however, it was reported that for model particles witli a low surface charge, where tire DL VO tlieory is expected to hold, tire aggregation kinetics do agree witli tire tlieoretical predictions (see [60], and references tlierein). [Pg.2684]

The suitability of the model reaction chosen by Brown has been criticised. There are many side-chain reactions in which, during reaction, electron deficiencies arise at the site of reaction. The values of the substituent constants obtainable from these reactions would not agree with the values chosen for cr+. At worst, if the solvolysis of substituted benzyl chlorides in 50% aq. acetone had been chosen as the model reaction, crJ-Me would have been —0-82 instead of the adopted value of —0-28. It is difficult to see how the choice of reaction was defended, save by pointing out that the variation in the values of the substituent constants, derivable from different reactions, were not systematically related to the values of the reaction constants such a relationship would have been expected if the importance of the stabilization of the transition-state by direct resonance increased with increasing values of the reaction constant. [Pg.139]

The accuracy and precision of FIA are comparable to that obtained by conventional methods of analysis. The precision of a flow injection analysis is influenced by variables that are not encountered in conventional methods, including the stability of the flow rate and the reproducibility of the sample s injection. In addition, results from FIA may be more susceptible to temperature variations. These variables, therefore, must be carefully controlled. [Pg.658]

For most vinyl polymers, head-to-tail addition is the dominant mode of addition. Variations from this generalization become more common for polymerizations which are carried out at higher temperatures. Head-to-head addition is also somewhat more abundant in the case of halogenated monomers such as vinyl chloride. The preponderance of head-to-tail additions is understood to arise from a combination of resonance and steric effects. In many cases the ionic or free-radical reaction center occurs at the substituted carbon due to the possibility of resonance stabilization or electron delocalization through the substituent group. Head-to-tail attachment is also sterically favored, since the substituent groups on successive repeat units are separated by a methylene... [Pg.23]

The processes used commercially for the manufacture of film and sheeting materials are generaUy similar in basic concept, but variations in equipment or process conditions are used to optimize output for each type of film or sheeting material. The nature of the polymer to be used, its formulation with plasticizers (qv), fillers (qv), flow modifiers, stabilizers, and other modifiers, as weU as its molecular weight and distribution are aU critical to the... [Pg.378]

CellgeometTy is governed predominantly by the final foam density and the external forces exerted on the cellular stmcture prior to its stabilization in the expanded state. In a foam prepared without such external forces, the cells tend to be spherical or ellipsoidal at gas volumes less than 70—80% of the total volume, and they tend toward the shape of packed regular dodecahedra at greater gas volumes. These shapes have been shown to be consistent with surface chemistry arguments (144,146,147). Photographs of actual foam cells (Fig. 2) show a broad range of variations in shape. [Pg.411]

Solvent variation can gready affect the acidity of hydantoins. Although two different standard states are employed for the piC scale and therefore care must be exercised when comparing absolute acidity constants measured in water and other solvents like dimethyl sulfoxide (DMSO), the huge difference in piC values, eg, 9.0 in water and 15.0 in DMSO (12) in the case of hydantoin itself, indicates that water provides a better stabilization for the hydantoin anion and hence an increased acidity when compared to DMSO. [Pg.250]

Catalytic Properties. In zeoHtes, catalysis takes place preferentially within the intracrystaUine voids. Catalytic reactions are affected by aperture size and type of channel system, through which reactants and products must diffuse. Modification techniques include ion exchange, variation of Si/A1 ratio, hydrothermal dealumination or stabilization, which produces Lewis acidity, introduction of acidic groups such as bridging Si(OH)Al, which impart Briimsted acidity, and introducing dispersed metal phases such as noble metals. In addition, the zeoHte framework stmcture determines shape-selective effects. Several types have been demonstrated including reactant selectivity, product selectivity, and restricted transition-state selectivity (28). Nonshape-selective surface activity is observed on very small crystals, and it may be desirable to poison these sites selectively, eg, with bulky heterocycHc compounds unable to penetrate the channel apertures, or by surface sdation. [Pg.449]


See other pages where Stability variation is mentioned: [Pg.29]    [Pg.245]    [Pg.158]    [Pg.7]    [Pg.386]    [Pg.292]    [Pg.155]    [Pg.48]    [Pg.226]    [Pg.412]    [Pg.213]    [Pg.1525]    [Pg.611]    [Pg.114]    [Pg.93]    [Pg.1805]    [Pg.29]    [Pg.245]    [Pg.158]    [Pg.7]    [Pg.386]    [Pg.292]    [Pg.155]    [Pg.48]    [Pg.226]    [Pg.412]    [Pg.213]    [Pg.1525]    [Pg.611]    [Pg.114]    [Pg.93]    [Pg.1805]    [Pg.585]    [Pg.702]    [Pg.189]    [Pg.2831]    [Pg.124]    [Pg.173]    [Pg.279]    [Pg.726]    [Pg.89]    [Pg.406]    [Pg.106]    [Pg.325]    [Pg.489]    [Pg.328]    [Pg.547]    [Pg.548]    [Pg.247]   
See also in sourсe #XX -- [ Pg.15 ]




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