Solubility argone

Argon is two and one half times as soluble in water as nitrogen, having about the same solubility as oxygen. Argon is colorless and odorless, both as a gas and liquid. Argon is considered to be a very inert gas and is not known to form true chemical compounds, as do krypton, xenon, and radon. 

It would clearly be of interest to discover how far the nonane method can be used with adsorbates other than nitrogen. A study along these lines has been carried out by Tayyab, but a discussion of his rather unexpected results is best deferred until the role of fine constrictions has been considered (p. 228). Meanwhile it may be noted that the applicability of the technique seems to be limited to adsorptives such as nitrogen or argon which have negligible solubility in solid or supercooled liquid n-nonane. 

Let us first consider the three-phase equilibrium ( -clathrate-gas, for which the values of P and x = 3/( +3) were determined at 25°C. When the temperature is raised the argon content in the clathrate diminishes according to Eq. 27, while the pressure can be calculated from Eq. 38 by taking yA values following from Eq. 27 and the same force constants as used in the calculation of Table III. It is seen that the experimental results at 60°C and 120°C fall on the line so calculated. At a certain temperature and pressure, solid Qa will also be able to coexist with a solution of argon in liquid hydroquinone at this point (R) the three-phase line -clathrate-gas is intersected by the three-phase line -liquid-gas. At the quadruple point R solid a-hydroquinone (Qa), a hydroquinone-rich liquid (L), the clathrate (C), and a gas phase are in equilibrium the composition of the latter lies outside the part of the F-x projection drawn in Fig. 3. The slope of the three-phase line AR must be very steep, because of the low solubility of argon in liquid hydroquinone. 

Coelenterazine analogues are easily soluble in methanol like coelenterazine. When methanol is used, however, the methanol concentration in the regeneration mixture should not exceed 5%. If the use of methanol must be avoided, dissolve the coelenterazine analogue in water with the help of a trace amount of 1M NaOH. However, coe-lenterazines in alkaline condition are extremely unstable. Therefore, the solution must be made rapidly in argon atmosphere and added at once to the regeneration mixture containing apoaequorin. 

The poor solubility of coelenterazine in neutral aqueous buffer solutions often hampers the use of this compound in biological applications. The simplest way to make an aqueous solution is the dilution of a methanolic 3 mM coelenterazine with a large volume of a desired aqueous buffer solution. If the use of alcoholic solvents is not permitted, dissolve coelenterazine in a small amount of water with the help of a trace amount of 1 M NaOH or NH4OH, and then immediately dilute this solution with a desired aqueous buffer solution. However, because of the rapid oxidation of coelenterazine in alkaline solutions, it is recommended that the procedure be carried out under argon gas and as quickly as possible. 

Properties of luciferin. The luciferin of Odontosyllis is a highly polar substance. It is soluble in water, methanol, and DMF, but practically insoluble in ra-butanol, ethyl acetate and acetonitrile. The luciferin is strongly adsorbed onto DEAE-cellulose, even under acidic conditions, indicating that the molecule possesses a strong acidic functionality. Although the luciferin is unstable in the presence of air, it is quite stable in dilute methanol under argon at — 20°C. 

Assuming a cooler temperature for helium, this means the amount of heat energy available for pyrolysis is less, which would produce less hydrocarbon products. This ultimately would lead to a relatively smaller SL quenching compared to that observed in argon saturated solutions. The relative change in bubble temperature would also be less in helium saturated solutions due to the lower amount of hydrocarbon products generated. Solubility differences would re-enforce this. 

Poly(iV-substituted dithieno[3,2-3 2, 3 -rf pyrroles (PDTPs) 167a,b) <2005MM4545>, a class of soluble (chiral) conjugated polymers with a stable oxidized state, were prepared by an oxidative coupling by FeClj in chloroform under an argon atmosphere. The crude material was reduced with hydrazine to afford compound 167 (Scheme 19) <2005MM4545>. 

Francesconi, K.A., P. Micks, R.A. Stockton, and K.J. Irgolic. 1985. Quantitative determination of arsenobe-taine, the major water-soluble arsenical in three species of crab, using high pressure liquid chromatography and an inductively coupled argon plasma emission spectrometer as the arsenic-specific detector. Chemosphere 14 1443-1453. 

Polyether 618 The sulfonium polyelectrolyte 617 was dissolved in a minimal amount of methanol. The solution was stirred for 1 week under argon, during which pendant polyether 618 precipitated from the solution. The tacky yellow material was completely soluble in CHC13 and THF. Polymer 618 can be dissolved in THF and passed through a 0.2-mm filter for GPC or for use in film casting and device fabrication. Cast films can be completely redissolved into CHC13 or THF. GPC in THF (polystryrene standards) gave A/w = 91,500 and Mn = 33,800. 

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