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Dispersion experimental

At the phenomenological level it may be known that Solvent A works well with acrylic dispersions while Solvent B is better for vinyl dispersions. Experimentally the important question of how much to add can be determined by systematic experimentation. However, for fine tuning some theoretical knowledge about the influence of transient solvent on the glass transition temperature (Tg), and tihe influence this will have on the minimum film forming temperature (MFT) is usefiil. This would undoubtedly lead to some consideration of the distribution (partitioning) of the solvent between the aqueous and polymer phases, which can be... [Pg.40]

Comparison between experimental determinations and theoretical curves is done in Figure 65.7. As it can be seen the dispersed experimental points are significantly included in the range 2.0 > e > 1.0, except those which have a low amount of hydroxyl. Such results are in favour of an increase of the probability of formation of a geminal after the formation of a single hydroxyl. Although the simplicity of the model, this underlines the importance of the local silicon structure on the hydration/dehydration process. This have been equally considered by Brinker et al. [12] who have shown the difference for strained and unstrained Si—O—Si bonds in such process. [Pg.857]

GCE/MWCNT-CHI, and (d) GCE/MWCNT-Naf modified with 1.0 mg ml" of CNT dispersion. Experimental conditions 5.0x10 M FcOH solution in 0.050M phosphate buffer... [Pg.95]

Also, many releases involve several chemical components or multiple effects. At this time the cumulative effects of simultaneous exposure to more than one material is not well understood. Are the effects additive, synergistic, or antagonistic in their effect on population As more information is developed on the characterization of multiple chemical component releases from source and dispersion experimentation and modeling, corresponding information is needed in the toxicology arena. Unfortunately, even toxic response data of humans to single component exposures are inadequate for a large number of chemical species. [Pg.243]

Griesing, M., Sedelmayer, R., Pauer, W., Moritz, H.-U. (2012). Acoustic levitation of dispersions Experimental setup and application. In First Working Party on Polymer Reaction Engineering, 12 October 2012. DOUA Campus University of Lyon, Fiance. [Pg.170]

Comparison of breakdown voltage (BDV) of polymer tantalum capacitors having polymer cathodes made by chemical in situ polymerization (typical range) and by polymer dispersions (experimental data points). Tantalum anodes were anodized at 100 V. [Pg.180]

Now consider some examples of the influence of sedimentation process upon PT sensitivity. Let us consider the application of fine-dispersed magnesia oxide powder as the developer. Using the methods described in [4] we experimentally determined the next characteristics of the developer s layer IT s 0,5, Re s 0,25 pm. We used dye sensitive penetrant Pion , which has been worked out in the Institute of Applied Physics of National Academy of Sciences of Belarus. Its surface tension ct = 2,5 10 N m V It can be shown that minimum width of an indication of magnesia powder zone, imbibed by Pion , which can be registered, is about W s 50 pm. Assume that n = 1. [Pg.615]

While the confirmation of the predicted long-range dispersion attraction between surfaces in air has been a major experimental triumph, the forces between particles in solution are of more general interest in colloid and surface chemistry. The presence of a condensed medium between the surfaces... [Pg.239]

Good, van Oss, and Caudhury [208-210] generalized this approach to include three different surface tension components from Lifshitz-van der Waals (dispersion) and electron-donor/electron-acceptor polar interactions. They have tested this model on several materials to find these surface tension components [29, 138, 211, 212]. These approaches have recently been disputed on thermodynamic grounds [213] and based on experimental measurements [214, 215]. [Pg.376]

The resonance vector analysis has been used to explore all of the questions raised above on the fate of the polyad numbers in larger molecules, the most thoroughly investigated case so far probably being C2FI2- This molecule has been very extensively probed by absorption as well as stimulated emission pumping and dispersed fluorescence teclmiques [, 53, 70 and 71], the experimental spectra have been analysed in... [Pg.73]

Diflfiisive processes nonnally operate in chemical systems so as to disperse concentration gradients. In a paper in 1952, the mathematician Alan Turing produced a remarkable prediction [37] that if selective diffiision were coupled with chemical feedback, the opposite situation may arise, with a spontaneous development of sustained spatial distributions of species concentrations from initially unifonn systems. Turmg s paper was set in the context of the development of fonn (morphogenesis) in embryos, and has been adopted in some studies of animal coat markings. With the subsequent theoretical work at Brussels [1], it became clear that oscillatory chemical systems should provide a fertile ground for the search for experimental examples of these Turing patterns. [Pg.1108]

While a laser beam can be used for traditional absorption spectroscopy by measuring / and 7q, the strength of laser spectroscopy lies in more specialized experiments which often do not lend themselves to such measurements. Other techniques are connnonly used to detect the absorption of light from the laser beam. A coimnon one is to observe fluorescence excited by the laser. The total fluorescence produced is nonnally proportional to the amount of light absorbed. It can be used as a measurement of concentration to detect species present in extremely small amounts. Or a measurement of the fluorescence intensity as the laser frequency is scaimed can give an absorption spectrum. This may allow much higher resolution than is easily obtained with a traditional absorption spectrometer. In other experiments the fluorescence may be dispersed and its spectrum detennined with a traditional spectrometer. In suitable cases this could be the emission from a single electronic-vibrational-rotational level of a molecule and the experimenter can study how the spectrum varies with level. [Pg.1123]

Fig. 5.37 Comparison of the calculated phonon dispersion curve for Al with the experimental values measured using neutron diffraction. (Figure redrawn from Michin Y, D Farkas, M ] Mehl and D A Papaconstantopoulos 1999. Interatomic Potentials for Monomatomic Metals from Experimental Data and ab initio Calculations. Physical Review 359 3393-3407.)... Fig. 5.37 Comparison of the calculated phonon dispersion curve for Al with the experimental values measured using neutron diffraction. (Figure redrawn from Michin Y, D Farkas, M ] Mehl and D A Papaconstantopoulos 1999. Interatomic Potentials for Monomatomic Metals from Experimental Data and ab initio Calculations. Physical Review 359 3393-3407.)...
Molecular chirality is most often observed experimentally through its optical activity, which is the elfect on polarized light. The spectroscopic techniques for measuring optical activity are optical rotary dispersion (ORD), circular di-chroism (CD), and vibrational circular dichroism (VCD). [Pg.113]

Validating the final experimental protocol was accomplished by running a model study in which Nd was released into the atmosphere from a 100-MW coal utility boiler. Samples were collected at 13 locations, all of which were 20 km from the source. Experimental results were compared with predictions determined by the rate at which the tracer was released and the known dispersion of the emissions. [Pg.8]

POWDERS,HANDLING - DISPERSION OF PO XTERS IN LIQUIDS] Pol 19) -among experimental variables pESIGN OF EXPERIMENTS] pol 7)... [Pg.840]

Chemical Reaction Measurements. Experimental studies of incineration kinetics have been described (37—39), where the waste species is generally introduced as a gas in a large excess of oxidant so that the oxidant concentration is constant, and the heat of reaction is negligible compared to the heat flux required to maintain the reacting mixture at temperature. The reaction is conducted in an externally heated reactor so that the temperature can be controlled to a known value and both oxidant concentration and temperature can be easily varied. The experimental reactor is generally a long tube of small diameter so that the residence time is well defined and axial dispersion may be neglected as a source of variation. Off-gas analysis is used to track both the disappearance of the feed material and the appearance and disappearance of any products of incomplete combustion. [Pg.57]

In the depolymeri2ed scrap mbber (DSR) experimental process, ground scrap mbber tines produce a carbon black dispersion in ok (35). Initially, aromatic oks are blended with the tine cmmb, and the mixture is heated at 250—275°C in an autoclave for 12—24 h. The ok acts as a heat-transfer medium and swelling agent, and the heat and ok cause the mbber to depolymeri2e. As more DSR is produced and mbber is added, less aromatic ok is needed, and eventually virtually 100% of the ok is replaced by DSR. The DSR reduces thermal oxidation of polymers and increases the tack of uncured mbber (36,37). Depolymeri2ed scrap mbber has a heat value of 40 MJ/kg (17,200 Btu/lb) and is blended with No. 2 fuel ok as fuel extender (38). [Pg.15]

Viscosity—Concentration Relationship for Dilute Dispersions. The viscosities of dilute dispersions have received considerable theoretical and experimental treatment, partly because of the similarity between polymer solutions and small particle dispersions at low concentration. Nondeformable spherical particles are usually assumed in the cases of molecules and particles. The key viscosity quantity for dispersions is the relative viscosity or viscosity ratio,... [Pg.173]


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See also in sourсe #XX -- [ Pg.881 ]




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Axial dispersion experimental correlations

Dielectric-experimental parameters Dispersion

Dispersability experimental methods

Dispersion coefficient experimental determination

Dispersion experimental correlations

Dispersion experimental data

Dispersion experimental determination

Dispersion experimental findings

Experimental Results for Dispersions

Experimental determination of dispersion coefficient from a pulse input

Experimental methods Taylor dispersion

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