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Self Liquids

Zaikin A N and Zhabotinsky A M 1970 Concentration wave propagation in two-dimensional liquid-phase self-oscillating system Nature 225 535-7... [Pg.1117]

The power of optical spectroscopies is that they are often much better developed than their electron-, ion- and atom-based counterparts, and therefore provide results that are easier to interpret. Furtlienuore, photon-based teclmiques are uniquely poised to help in the characterization of liquid-liquid, liquid-solid and even solid-solid interfaces generally inaccessible by other means. There has certainly been a renewed interest in the use of optical spectroscopies for the study of more realistic systems such as catalysts, adsorbates, emulsions, surfactants, self-assembled layers, etc. [Pg.1779]

The parameter /r tunes the stiffness of the potential. It is chosen such that the repulsive part of the Leimard-Jones potential makes a crossing of bonds highly improbable (e.g., k= 30). This off-lattice model has a rather realistic equation of state and reproduces many experimental features of polymer solutions. Due to the attractive interactions the model exhibits a liquid-vapour coexistence, and an isolated chain undergoes a transition from a self-avoiding walk at high temperatures to a collapsed globule at low temperatures. Since all interactions are continuous, the model is tractable by Monte Carlo simulations as well as by molecular dynamics. Generalizations of the Leimard-Jones potential to anisotropic pair interactions are available e.g., the Gay-Beme potential [29]. This latter potential has been employed to study non-spherical particles that possibly fomi liquid crystalline phases. [Pg.2366]

Manne S 1997 Visualizing self-assembly Force microscopy of ionic surfactant aggregates at solid-liquid interfaces Prog. Colloid Polym. Sol. 103 226-33... [Pg.2607]

The conclusion of all these thermodynamic studies is the existence of thiazole-solvent and thiazole-thiazole associations. The most probable mode of association is of the n-rr type from the lone pair of the nitrogen of one molecule to the various other atoms of the other. These associations are confirmed by the results of viscosimetnc studies on thiazole and binary mixtures of thiazole and CCU or QHij. In the case of CCU, there is association of two thiazole molecules with one solvent molecule, whereas cyclohexane seems to destroy some thiazole self-associations (aggregates) existing in the pure liquid (312-314). The same conclusions are drawn from the study of the self-diffusion of thiazole (labeled with C) in thiazole-cyclohexane solutions (114). [Pg.88]

Liquid crystal polyesters are made by a different route. Because they are phenoHc esters, they cannot be made by direct ester exchange between a diphenol and a lower dialkyl ester due to unfavorable reactivities. The usual method is the so-called reverse ester exchange or acidolysis reaction (96) where the phenoHc hydroxyl groups are acylated with a lower aHphatic acid anhydride, eg, acetic or propionic anhydride, and the acetate or propionate ester is heated with an aromatic dicarboxyHc acid, sometimes in the presence of a catalyst. The phenoHc polyester forms readily as the volatile lower acid distills from the reaction mixture. Many Hquid crystal polymers are derived formally from hydroxyacids (97,98) and thein acetates readily undergo self-condensation in the melt, stoichiometric balance being automatically obtained. [Pg.295]

By-Products. Almost all commercial manufacture of pyridine compounds involves the concomitant manufacture of various side products. Liquid- and vapor-phase synthesis of pyridines from ammonia and aldehydes or ketones produces pyridine or an alkylated pyridine as a primary product, as well as isomeric aLkylpyridines and higher substituted aLkylpyridines, along with their isomers. Furthermore, self-condensation of aldehydes and ketones can produce substituted ben2enes. Condensation of ammonia with the aldehydes can produce certain alkyl or unsaturated nitrile side products. Lasdy, self-condensation of the aldehydes and ketones, perhaps with reduction, can lead to alkanes and alkenes. [Pg.333]

ThioglycoHc acid can be identified by its in spectmm or by gas chromatography. Most of the by-products and self-esterification products are also detected by liquid chromatography, eg, thiodiglycolic acid, dithiodiglycolic acid, linear dimers, and polymers. Iron content can be assayed by the red sensitive complex of 1,10-phenanthroline [66-71-7] and ferrous ion of a mineralised sample. Ferric ion turns an aqueous ammonia solution deep red-violet. [Pg.4]

Liquid ethylene oxide under adiabatic conditions requires about 200°C before a self-heating rate of 0.02°C/min is observed (190,191). However, in the presence of contaminants such as acids and bases, or reactants possessing a labile hydrogen atom, the self-heating temperature can be much lower (190). In large containers, mnaway reaction can occur from ambient temperature, and destmctive explosions may occur (268,269). [Pg.465]

In the special case that A and B are similar in molecular weight, polarity, and so on, the self-diffusion coefficients of pure A and B will be approximately equal to the mutual diffusivity, D g. Second, when A and B are the less mobile and more mobile components, respectively, their self-diffusion coefficients can be used as rough lower and upper bounds of the mutual diffusion coefficient. That is, < D g < Dg g. Third, it is a common means for evaluating diffusion for gases at high pressure. Self-diffusion in liquids has been studied by many [Easteal AIChE]. 30, 641 (1984), Ertl and Dullien, AIChE J. 19, 1215 (1973), and Vadovic and Colver, AIChE J. 18, 1264 (1972)]. [Pg.592]

Lee-Thodos presented a generahzed treatment of self-diffusivity for gases (and liquids). These correlations have been tested for more than 500 data points each. The average deviation of the first is 0.51 percent, and that of the second is 17.2 percent. 8 = PyVr, s/cm and where G = (X - X)/(X - 1), X = p,/T h and X = p /T evaluated at the solid melting point. [Pg.595]

Many more correlations are available for diffusion coefficients in the liquid phase than for the gas phase. Most, however, are restiicied to binary diffusion at infinite dilution D°s of lo self-diffusivity D -. This reflects the much greater complexity of liquids on a molecular level. For example, gas-phase diffusion exhibits neghgible composition effects and deviations from thermodynamic ideahty. Conversely, liquid-phase diffusion almost always involves volumetiic and thermodynamic effects due to composition variations. For concentrations greater than a few mole percent of A and B, corrections are needed to obtain the true diffusivity. Furthermore, there are many conditions that do not fit any of the correlations presented here. Thus, careful consideration is needed to produce a reasonable estimate. Again, if diffusivity data are available at the conditions of interest, then they are strongly preferred over the predictions of any correlations. [Pg.596]

Matthews-Akgerman The free-volume approach of Hildebrand was shown to be valid for binary, dilute liquid paraffin mixtures (as well as self-diffusion), consisting of solutes from Cg to Cig and solvents of Cg and C o- The term they referred to as the diffusion volume was simply correlated with the critical volume, as = 0.308 V. We can infer from Table 5-15 that this is approximately related to the volume at the melting point as = 0.945 V, . Their correlation was vahd for diffusion of linear alkanes at temperatures up to 300°C and pressures up to 3.45 MPa. Matthews et al. and Erkey and Akger-man completea similar studies of diffusion of alkanes, restricted to /1-hexadecane and /i-octane, respectively, as the solvents. [Pg.598]

A regulator is a compact device that maintains the process variable at a specific value in spite of disturbances in load flow. It combines the functions of the measurement sensor, controher, and final control element into one self-contained device. Regulators are available to control pressure, differential pressure, temperature, flow, hquid level, and other basic process variables. They are used to control the differential across a filter press, heat exchanger, or orifice plate. Regulators are used for monitoring pressure variables for redundancy, flow check, and liquid surge relief. [Pg.793]

Tanks cool and partially freeze solids form a layer of self-insulation. This complex case, which has been known to occur with heavy hydrocarbons and mixtures of hydrocarbons, has been discussed by Stnhlbarg [Pet. Refiner,. 38, 143 (Apr. 1, 1959)]. The contents in the center of snch tanks have been known to remain warm and liquid even after several years of cooling. [Pg.1049]

The principal advantage of self-induced spray scrubbers is the efim-ination of a pump for recirculation of the scrubbing liquid. However, the designs for high-energy service are somewhat more complex and less flexible than those for venturi scrubbers. [Pg.1594]

SelF-siipported cylindrical membranes For liquid separations are made From 250 jlrn up to 6 rnrn, but there is no obvious limit to Future oFFerings. Membrane devices For liquids are almost alvvws tube-side Feed, with tw o major exceptions at the extremes oF porositv. High-pressure RO is almost always shell-side Feed, and one supplier oF verv lovv -pressiire MF also rims with shell-side Feed. [Pg.2026]

Self-Generated Discharges Vapor-air mixtures can be ignited by sparks from highly charged liquids. It is said that such liquids cany their own match. Typical causes of such charging for poorly conductive (<50 pS/m) liquids include ... [Pg.2334]

The main supramolecular self-assembled species involved in analytical chemistry are micelles (direct and reversed), microemulsions (oil/water and water/oil), liposomes, and vesicles, Langmuir-Blodgett films composed of diphilic surfactant molecules or ions. They can form in aqueous, nonaqueous liquid media and on the surface. The other species involved in supramolecular analytical chemistry are molecules-receptors such as calixarenes, cyclodextrins, cyclophanes, cyclopeptides, crown ethers etc. Furthermore, new supramolecular host-guest systems arise due to analytical reaction or process. [Pg.417]

Autoignition Temperature (AIT) The auto ignition temperature of a substanee, whether solid, liquid, or gaseous, is the minimum temperature required to initiate or eause self-sustained eombustion, in air, with no other souree of ignition. [Pg.159]

Table 10.1 Self diffusion coefficients of some liquid metals expressed by an Arrhenius equation... Table 10.1 Self diffusion coefficients of some liquid metals expressed by an Arrhenius equation...
Double seals require some type of support system. The reason is simple. With two seals mounted onto the same shaft, one seal is the principal or primary seal and the other becomes the secondary or back up seal already installed. If the primary seal is performing its function and sealing the pumped liquid, the. secondary. seal would be running dry, overheat, burn and self-destruct. Then when the crucial moment comes, we won t have a second seal to assume the ftinctions, which was the original reason to consider a dual seal. [Pg.198]


See other pages where Self Liquids is mentioned: [Pg.26]    [Pg.166]    [Pg.26]    [Pg.166]    [Pg.30]    [Pg.297]    [Pg.406]    [Pg.466]    [Pg.621]    [Pg.1704]    [Pg.2218]    [Pg.2376]    [Pg.2624]    [Pg.397]    [Pg.211]    [Pg.292]    [Pg.202]    [Pg.533]    [Pg.257]    [Pg.401]    [Pg.291]    [Pg.597]    [Pg.1442]    [Pg.1594]    [Pg.2217]    [Pg.2220]    [Pg.2313]    [Pg.2317]    [Pg.2435]    [Pg.291]   
See also in sourсe #XX -- [ Pg.177 ]




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