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Solidification partial

Note 2. Further cooling may result in partial solidification. [Pg.226]

Flare systems must be protected against any possibility of partial or complete blockage by ice, hydrates, solidification, etc. Seal Drums and Y-seals requiring winterizing should be provided with temperature-controlled steam injection to maintain the seal water temperature at 4 to 10 C. This limits the quantity of water vapor entering the flare stack. [Pg.283]

Fig. 5. A growth model of a nanocapsule partially filled with a crystallite of rare-earth carbide (RCj for R = Y, La,. . . , Lu R,C4 for R = Sc) (a) R-C alloy particles, which may be in a liquid or quasi-liquid phase, are formed on the surface of a cathode (b) solidification (graphitizalion) begins from the surface of a particle, and R-enriched liquid is left inside (c) graphite cage outside equilibrates with RCj (or R3C4 for R = Sc) inside. Fig. 5. A growth model of a nanocapsule partially filled with a crystallite of rare-earth carbide (RCj for R = Y, La,. . . , Lu R,C4 for R = Sc) (a) R-C alloy particles, which may be in a liquid or quasi-liquid phase, are formed on the surface of a cathode (b) solidification (graphitizalion) begins from the surface of a particle, and R-enriched liquid is left inside (c) graphite cage outside equilibrates with RCj (or R3C4 for R = Sc) inside.
The theory of seaweed formation does not only apply to solidification processes but in fact to the completely different phenomenon of a wettingdewetting transition. To be precise, this applies to the so-called partial wetting scenario, where a thin liquid film may coexist with a dry surface on the same substrate. These equations are equivalent to the one-sided model of diffusional growth with an effective diffusion coefficient which depends on the viscosity and on the thermodynamical properties of the thin film. [Pg.895]

A mixture of 2.33 g of bismuth oxide (BijOa), 3.71 g of anhydrous sodium carbonate, and 7.64 g of triglycollamic acid and 40 cc of water was heated at B0°C on the water bath until all was dissolved. The solution was avaporated on the water bath to a syrup. The syrup was allowed to cool, during which time partial solidification occurred. It was then triturated with 300 cc of alcohol, and the solid anhydrous salt was collected on a filter, washed with alcohol, ground fine, and dried in a vacuum desiccator. This substance has a water solubility at 25°C of 31 S% by weight. It decomposes on heating in the melting point bath. [Pg.180]

The molecular structure of Li-, Na-, and K-silicates in 0.2 to 3 mole SiOj/L aqueous solutions has been investigated by FTIR and Raman spectroscopy to help exploring their solidification process. These silicates were found to be only partially dissociated and their average molecular weight (AMW) varies with the type of the alkaline ion, the alkaline/silicon ratio, and the concentration. It is demonstrated that these differences are associated with differences in the Qn connectivity ratios of [Si04] tetrahedra and in the dominating siloxane ring structures which can be identified by their vibrational spectra. [Pg.35]

Partial Solidification prior to Impact Parti al solidification of an impacting droplet prior to impact is considered. [Pg.303]

Group 4 Partial Solidification prior to Impact Analytical- Numerical San Marchi et al.11571... [Pg.305]

Madejski s solidification model did not account for partial solidification of a droplet prior to impact. San Marchi et al.[157]... [Pg.313]

However, V4+ compounds still play an important role for the activity of the catalyst because an equilibrium exists between V5+ and V4+ compounds in the melt. The degree of reduction to inactive V4+ increases at low temperature and high S02 partial pressure, and it has also been found to depend on the liquid dispersion on the support [9], Furthermore, at temperatures below 500°C some V4+ compound precipitates and gradually depletes the melt of V5+ when the temperature is lowered, and this partial solidification eventually causes the activity to drop to practically zero at some minimum operating temperature of about 350°C. [Pg.317]

The freeze concentration process is based on the partial solidification of water into ice in a fluid food product followed by the removal of the solid ice phase from the concentrated liquid phase. This process has some inherent advantages over evaporation and reverse osmosis for concentrating fluid foods as well as other process streams (1). One advantage is that essentially none... [Pg.316]

The very fact that the vapor phase of many substances can condense to form a liquid is a consequence of the existence of attractive van der Waals forces between atoms or molecules. An attractive intermolecular force is not needed for a gas to condense into a solid solidification can occur purely as a result of excluded-volume interactions among the molecules at sufficiently large densities. The pressure in a fluid, the cohesion between materials, and the existence of surface energy or surface tension all result, partially or wholly, from van der Waals forces. [Pg.463]


See other pages where Solidification partial is mentioned: [Pg.13]    [Pg.79]    [Pg.235]    [Pg.16]    [Pg.24]    [Pg.853]    [Pg.309]    [Pg.471]    [Pg.1215]    [Pg.242]    [Pg.145]    [Pg.217]    [Pg.102]    [Pg.211]    [Pg.313]    [Pg.314]    [Pg.93]    [Pg.561]    [Pg.250]    [Pg.555]    [Pg.576]    [Pg.55]    [Pg.204]    [Pg.281]    [Pg.717]    [Pg.187]    [Pg.118]    [Pg.242]    [Pg.319]    [Pg.13]    [Pg.14]    [Pg.79]    [Pg.848]    [Pg.872]   
See also in sourсe #XX -- [ Pg.314 ]




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Partial Solidification Prior to Impact

Solidification

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