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Water kinetic viscosity

Conversion between Kinetic Viscosity and Absolute Viscosity for Water... [Pg.751]

Figure 15.5 Isotherms of the kinetic viscosity, ri/p, of water as a function of pressure. Data... Figure 15.5 Isotherms of the kinetic viscosity, ri/p, of water as a function of pressure. Data...
Aerated water flows down a mbe with an inside diameter of 19 mm. The Reynolds number is 42,000. The corrosion rate is controlled by the rate of mass transport of oxygen, whose concentration in the water is equal to 7 mg 1 . The kinetic viscosity of water is equal to 0.01 cm s. Calculate the corrosion current density of the metal walls of the tube. [Pg.595]

The liquid is a fluorinated oil called PFAS (polyfluoromethylalkylsilox-ane). Since the dewetting kinetics of water is far too rapid to be observable with a regular camera, PFAS is a much better choice. It dewets much more slowly and does not dissolve PDMS. The number of monomers of this fluoro-silicone determines its viscosity, which is 100 to 1,000 times higher than that of water. Experiments with a fast camera show that water obeys the same laws. [Pg.244]

Kinetics of water absorption by ionic liquids has been found to be relatively complex. They neither follow sinple first-order nor second-order rate equations. At every stage of water absorption, the physical properties (e.g. polarity, viscosity, etc.) change at the molecular level. [Pg.258]

Where Sh is Sherwood number [-], Re is Reynolds number [-], Sc is Schmidt number [-], is liquid-phase-mass-transfer coefficient [m-s ], d] is diameter of a stirrer [m], D is diffusion coefficient [m - s ], n is agitation speed [s ], V is kinetic viscosity of water [m - s ] and i is chemical species. Sc was varied by adding propylene glycol in the solution. Then the value of At,i for limestone dissolution was evaluated by Eq. 4, in which D[ and n were varied with experimental condition while V and c/l were constant. [Pg.25]

Post-Gel Examples. In addition to affecting the pre-gel viscosity, the presence of water (or humidity during cure) can also affect the cure response and final network structure formed in urethane coatings. Using reactions R1-R4, the following kinetic scheme can be written for cure of polyol-urethane coatings in the presence of humidity ... [Pg.200]

The model proposed by Menger et al. (Fig. 2) shows two extreme conformations, one in which the hydrocarbon chains are fully extended and another in which they are folded [18, 19], The surface of Menger s micelle is less defined than in the classical model and the surfactants that form the micelle are randomly orientated. The water can penetrate and enter in contact with the hydrophobic part of the surfactants. This model, apart from being more acceptable from an esteric point of view, gives a better explanation than the classical model of a series of experimental results such as viscosity, polarity, or kinetics. [Pg.291]

Viscosity measurements were made with two Cannon-Ubbelohde viscometers, and timing was by an optical device actuating an electronic timer (Wescan Instruments, Inc.). An air thermostat was used. The viscometers were calibrated with redistilled air-saturated water over the range 10°-50°C. The kinetic-energy correction was used in the form ... [Pg.338]

In several previous papers, the possible existence of thermal anomalies was suggested on the basis of such properties as the density of water, specific heat, viscosity, dielectric constant, transverse proton spin relaxation time, index of refraction, infrared absorption, and others. Furthermore, based on other published data, we have suggested the existence of kinks in the properties of many aqueous solutions of both electrolytes and nonelectrolytes. Thus, solubility anomalies have been demonstrated repeatedly as have anomalies in such diverse properties as partial molal volumes of the alkali halides, in specific optical rotation for a number of reducing sugars, and in some kinetic data. Anomalies have also been demonstrated in a surface and interfacial properties of aqueous systems ranging from the surface tension of pure water to interfacial tensions (such as between n-hexane or n-decane and water) and in the surface tension and surface potentials of aqueous solutions. Further, anomalies have been observed in solid-water interface properties, such as the zeta potential and other interfacial parameters. [Pg.77]


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