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The solubilities of some acidic gases in chloride melts

The solubilities of substances having the empirical formula SiC 2 or SiC 2 1H2O have been studied for decades. These studies are much more complicated than they appear, because of the reluctance of soluble silica to reach equilibrium or even metastable equilibrium with its solid phases. Soluble silica tends to polymerize slowly in supersaturated solutions rather than to precipitate cleanly. In addition, the solid phase that precipitates is often amorphous silica instead of the most stable phase, quartz or its close relative chert. Amorphous silica is metastable and much more soluble than quartz. The solubilities of amorphous silica and quartz are often assumed to be the upper and lower limits of silica solubility in soils. Viewed from the range of soil solution compositions shown in

The solubilities of the aqueous rare earth perchlorates at 25 C .

The solubility

The solubility area of water in a hydrocarbon solution at 30 C. Key

The solubility constant as a function of the recipro-

The solubility curve

The solubility curves 1 CAH, 2 C AHj, 3 AHj gel, 4 microcrystalline AHj, 5 gibbsite. There is also shown the inteiseclion point , corresponding to the CA solubility. The supersaturation curves

The solubility curves of the rare-earth orthophosphates in Pb2P207 are shown plotted from the data of Eigermaim et al. . The solubility shows a decrease with increasing atomic number of the rare-earth elements, although the differences in solubihty between neighboring elements are relatively small.

The solubility data for NPl and

The solubility dependence of trilysyl insulin, a chemically modified insulin with an isoelectric point of 7.4 compared with the isoelectric point of unmodified insulin of 5.3.

The solubility enhancement as a function of particle diameter for three hypothetical compounds with surface energies of 50,75, and 100 mN m does not increase significantly until particle diameters reach below 75 nm for drags with a surface energy of 50 mN m. Source

The solubility enhancement of DR at different non-ionic surfactants 114

The solubility enhancement of DR at different non-ionic surfactants. In all cases, excess amount of DR was added to the 10 mM of surfactants unit a stable solubilized DR formed.

The solubility function expected for the combination of the above-mentioned physicochemical effects .

The solubility isotherm in the hydroquinone - HCOOH - CH3CN system .

The solubility limit for aluminum versus reciprocal temperature as extracted from SIMS measurement of out-diffusion from heavily doped 4H-SIC .

The solubility of a nonvolatile solid in a supercritical fluid, as a function cf pressure at two temperatures close to the critical temperature of the system

The solubility of a poorly soluble compound mixed with lecithin in two different ratios, 2.5

The solubility of AgCI in aqueous KCI.

The solubility of AgSCN in KSCN solutions. Circles, data. Dashed line, calculated from equation . Straight extension for simple behavior, no complexing. Square, pure water solubility.

The solubility of amorphous silica against pH at 303 K. The full and dotted lines show the original and alkali-treated materials, respectively.

The solubility of amorphous silica as a function of pH.45

The solubility of an Ionic surfactant Is proportional to a minimum water content.

The solubility of benzaldehyde and benzyl alcohol in CO2 at 318.2 K and different pressures calculated from PR equation of state Benzaldehyde, O Benzyl alcohol.



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