Solvent volume

Tyn-Calus This correlation requires data in the form of molar volumes and parachors = ViCp (a property which, over moderate temperature ranges, is nearly constant), measured at the same temperature (not necessarily the temperature of interest). The parachors for the components may also be evaluated at different temperatures from each other. Quale has compiled values of fj for many chemicals. Group contribution methods are available for estimation purposes (Reid et al.). The following suggestions were made by Reid et al. The correlation is constrained to cases in which fig < 30 cP. If the solute is water or if the solute is an organic acid and the solvent is not water or a short-chain alcohol, dimerization of the solute A should be assumed for purposes of estimating its volume and parachor. For example, the appropriate values for water as solute at 25°C are = 37.4 cmVmol and yn = 105.2 cm g Vs mol. Finally, if the solute is nonpolar, the solvent volume and parachor should be multiplied by 8 Ig. 

Properties of Different Solvents. Volumes in Aqueous Solution. The Increment in Volume for a Pair of Ions. Volumes in Different Solvents Compared. Thermal Expansion. 

Analysis calculated for C1SH36N2O4S C, 57.41 H, 9.63 N, 7.43 S, 8.51. Found C, 57.60 H, 9.66 N, 7.37 S, 8.25. Thin-layer chromatograms (Note 10) run by the submitters showed a single spot for the product in each of three following solvent systems (solvents, volume ratio of solvents in the same order) chloroform-methanol-acetic acid, 85 10 5, Rf 0.60 1-butanol-acetic acid-water, 4 1 1, Rf 0.58 l-butanol acetic acid-pyridine-water, 15 3 10 12, Rf 0.71. 

The literature reports [a]n +23.2° (c = l, aqueous 5N hydrochloric acid). The product was analyzed by the submitters. Analysis caleulated for C5H11NO2S C, 40.25 H, 7.43 N, 9.39 S, 21.49. Found C, 40.14 H, 7.42 N, 9.50 S, 21.52. The product was homogeneous according to thin-layer chromatograms on precoated silica gel G plates purchased from Analtech, Inc., Newark, Delaware, and developed with the following two solvent systems (solvents, volume ratios of solvents in the same order) 1-butanol-acetic acid-ethyl acetate-water, 1 1 1 1, Rf 0.49 1-butanol-acetic acid-pyridine-water, 15 3 10 12, R/0.51. 

Hand rinsings Rinsing of hands twice with hexane solvent volume reduction fractionation and clean-up on Florisal GC/ECD No data No data Kazen et al. 1974... 

Chlorofonn is too non-polar to dissolve the phenolic compounds under study, but it dissolves many of the monoterpenes, at least to some extent. Because the solubility of some monoterpenes into chloroform was low, different solvent/ solid ratios were tested. These were 50,20,10 and 5 1/kg of dry phloem. The extracts were bright yellow and the strongest colour was with the smallest solvent/solid ratio (51/kg). The colour of the solvent indicated that the solubility of the extractable compounds was not restricting the reaction even with the smallest solvent volume. The taste of the dry samples was evaluated by comparing them to the original phloem sample. The results showed that the mildest taste was in the phloem extracted with a solvent/solid ratio of 50 1/kg and 20 1/kg also had some effect on the taste. The taste of the chloroform-extracted phloem was stabile and it was the same after a week. 

Inspect the culture tubes in the manifold to determine if there is water in the organic eluent for any sample. If a water layer is present, quantitatively transfer the organic phase into a clean culture tube using a small amount of additional solvent as necessary. Return the culture tube containing the organic extract to its proper location in the manifold rack. Remove the Cig and sodium sulfate mbes, and reinstall the silica tubes on the manifold. With the sample remaining in the culture tube, continue to apply vacuum to the manifold to remove excess solvent. When the solvent volume is < 1 mL, discontinue vacuum, and allow the sample to return to room temperature. Adjust the sample volume in the culture mbe to 1 mL with isooctane-ethyl acetate (9 1, v/v). Transfer the entire sample into an autosampler vial for GC/MS analysis. Sample extracts may be stored for up to 1 month in a refrigerator (< 10 °C) before analysis. 

All aspects in the analytical process are equally important, and each step should be isolated in method development experiments and/or validation to ensure acceptable quality of results. A good way to evaluate robustness of a method is to alter parameters (e.g., solvent volumes, temperature, pH, sources of reagents) of each step to determine... 

The magnitude of the pressure wave depends on the saaple size. It aay also prolong the duration of the pressure wave. If the sane anount of substance is injected in different solvent volumes, the peak areas will not necessarily be the same. 

Unfortunately, the preset split flow ratio is only an approximate indication of the sample split ratio. The latter depends in a complex way on many parameters, including the range of sample volatilities, sample solvent, volume of sample injected. 

Solubilizing all or part of a sample matrix by contacting with liquids is one of the most widely used sample preparation techniques for gases, vapors, liquids or solids. Additional selectivity is possible by distributing the sample between pairs of immiscible liquids in which the analyte and its matrix have different solubilities. Equipment requirements are generally very simple for solvent extraction techniques. Table 8.2 [4,10], and solutions are easy to manipulate, convenient to inject into chromatographic instruments, and even small volumes of liquids can be measured accurately. Solids can be recovered from volatile solvents by evaporation. Since relatively large solvent volumes are used in most extraction procedures, solvent impurities, contaminants, etc., are always a common cause for concern [65,66]. 

The classical Soxhlet extraction technique has seen some improvements, mainly in the submersion of the whole extraction thimble into the boiling extraction solvent, degree of automation, and in reduction of solvent volume. In a recently introduced universal extraction system (Biichi) four SLE methods are contained in one device Soxhlet Standard, Soxhlet warm, hot extraction and continuous flow. It is possible to use solvents with boiling points of up to 150 °C inert gas can be supplied during the extraction process. 

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