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Water with 10% methanol

The kinetics of Zn(II) electroreduction in water-methanol mixtures containing 1 M NaCl04 and TU was also investigated as a function of temperature [62]. The values of activation energy of Zn(II) electroreduction in these mixtures reached a maximum in the solution with 20 vol % of methanol. The apparent and true rate constants of the first and second electron charge transfer of Zn(II) electroreduction on Hg electrode in aqueous solution, and in the mixtures of water with methanol 91 vol %, DMSO 70 vol %, and DMF 90 vol % containing TU were estimated [63]. [Pg.733]

P. Dalager, Vapor-Liquid Equilibria of Binary Systems of Water with Methanol and Ethanol at Extreme Dilution of the Alcohols , J. Chem. Eng. Data, 14, 298-301 (1969). [Pg.157]

Follow Example 10.7. Replace the methyl group with a phenyl group (Ph) and water with methanol ... [Pg.195]

Issaq and McNitt [585] published a computer program for peak recognition on the basis of peak areas. They investigated the reproducibility of the area of some well-separated peaks for three solutes (anthraquinone, methyl anthraquinone and ethyl anthraquinone) in the 10 solvents used for their optimization procedure. The solvents included binary, ternary and quaternary mixtures of water with methanol, acetonitrile and THF. The areas were found to be reproducible within about 2 percent. The wavelength used for the UV detector in this study was not reported. [Pg.238]

Heteroselective solvation was also found in the system ZnCl2—N2H4-H20 The values of A remain much smaller in the case of insignificant selective solvation or of homoselective solvation. Further experiments have been performed in mixtures of water with methanol and acetonitrile ... [Pg.141]

Washburn numbers of hydrochloric acid and of alkali-metal halides have been determined in mixtures of water with methanol ethanol ... [Pg.143]

Bakalyar et al. 7 found that the selectivity of eluents containing mixtures of water with methanol, acetonitrile or tetrahydrofuran varied for different functional groups.The selectivity could be varied by using ternary solvents. The selectivity of a reversed-phase separation on alkyl bonded phases could best be varied by altering the mobile phase the nature of the alkyl group had only limited influence on the selectivity. [Pg.225]

In sections 6.6 and 6.7, we analyzed the conditions of stability using the parameter pAAB as a measure of the deviations from SI solutions. When Aab = 0> we had symmetrical ideal SI solutions. We found that for positive values of Aab, the system was always stable. For large negative values of A g, we found regions of instability. This conclusion seems to conflict with the experimental results that positive deviations from Raoult s law lead to instability. The classical examples shown in many books are mixtures of water and various normal alcohols. We reproduce the relevant curves in figure P. 1. Here, we plot the relative partial pressure of the alcohols in mixtures of water with methanol, ethanol, propanol and n-butanol. Clearly, in all of the four cases, deviations from Raoult s law as measured by either the quantities... [Pg.368]

The method description will certainly state the column you should use for your work. If not, refer to Tip No. 2. The most popular column material (stationary phase) is a C,g-modified silica gel. This stationary phase and the corresponding mobile phase most often consist of mixtures of water with methanol or acetonitrile, and we are then dealing with reversed-phase chromatography. The mobile phase can also contain additives or buffers. [Pg.7]

Frequency is 26 kHz Flow rates up to 50 L/h Liquids used must be either distilled water or solutions of water with methanol and glycerin... [Pg.578]

Measurements of the PEG brush thickness in an aqueous environment by optical and gravimetric methods enabled us to determine that they typically contain around 80% water, with this proportion decreasing as the quaffty of the solvent is decreased (replacing water with methanol or higher alcohols, for example). A good correlation between the solvent quality and the resulting friction (as measured by AFM) was found (2.11). [Pg.95]

The liquid-liquid extraction procedure tends to be tedious, but if properly conducted it is very quantitative and it can be used to extract quite large quantities of material. Typical aqueous phases are water alone and mixtures of water with methanol, ethanol or propan-2-ol, while typical non-aqueous phases are petroleum ether or other hydrocarbons, diethyl ether, chloroform and butanols. It is used chiefly to extract fatty alcohols and ethoxylates, fatty acids, fatty amines and alkanolamides from mixtures containing more polar surfactants, but the possible range of uses is much wider than this. [Pg.38]

The mobile phases used depend on both analytes and detection method. Those used most frequently are based on mixtures of water with methanol or acetonitrile made alkaline by the addition of ammonium carbonate, ammonium carbamate. [Pg.4399]

Here the IN term permits allowance to be made for the nucleophilicity (iV) of the solvent. The kinetics of aquation of the /r[Pg.242]

C. L. De Ligny and N. G. Van der Veen, Rec. Trav. Chim., 90, 984 (1971). Solubilities of some tetra-alkyl carbon, -silicon, -germanium, and -tin compounds in mixtures of water with methanol, ethanol, dioxane, acetone and acetic acid and differences between the standard chemical potentials of these solutes in their solutions in water and in the mixed or nonaqueous solvents at 25°C. [Pg.828]

When ethanoi is present, the risk of separation is much less than with methanol. Nevertheless, the ethanol should be relatively anhydrous (less than 3000 ppm water) moreover, if a fuel containing ethanol comes in contact with a water layer, a migration of ethanol toward the water is observed creating a fuel quality problem manifested by lower octane number and an environmental quality problem in that the water will need to be treated. Distribution of ethanol-based fuels requires extra precaution to ensure dryness in distribution systems. [Pg.244]

Make a theoretical plot of surface tension versus composition according to Eq. III-53, and compare with experiment. (Calculate the equivalent spherical diameter for water and methanol molecules and take o as the average of these.)... [Pg.95]

The glycine so obtained is almost pure. To remove traces of ammonium chloride, however, dissolve the glycine in 30 ml. of water, and then reprecipitate by the addition of 200 ml. of methanol. Cool the product in ice-water with stirring, and then... [Pg.130]

RCH=N—ONa and R R C=N—ONa) which may be filtered off and washed with methanol to remove traces of sodium methoxide. It should be kept moist with methanol the sodium derivative, if allowed to dry, may become very explosive. Also, upon contact with a trace of water, it is liable to decompose with explosive violence. The sodium derivative may be dissolved by successively adding small quantities to cold water with continual stirring. [Pg.531]


See other pages where Water with 10% methanol is mentioned: [Pg.133]    [Pg.82]    [Pg.162]    [Pg.287]    [Pg.78]    [Pg.13]    [Pg.160]    [Pg.363]    [Pg.1121]    [Pg.164]    [Pg.613]    [Pg.218]    [Pg.613]    [Pg.387]    [Pg.397]    [Pg.163]    [Pg.142]    [Pg.72]    [Pg.242]    [Pg.244]    [Pg.84]    [Pg.611]    [Pg.327]    [Pg.141]    [Pg.259]    [Pg.259]    [Pg.1170]    [Pg.133]    [Pg.855]   


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Methanol-water

With methanol

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