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Alcohols vapor pressure

The vapor pressure at the boiling point of a pure solvent is equal to atmospheric pressure. When solvents are used in mixtures or solutions, the vapor pressure is affected by other components present in the mixture. For example, if a solvent is hydrophilic, the addition of a hydrophilic solute decreases the vapor pressure. The addition of a hydrophobic solute to a hydrophilic solvent increases the vapor pressure. Alcohols have hydrophobic chains, therefore addition of small quantities of alcohol to water increases vapor pressure of resulting solution. Because of these phenomena and other types of associations between solvents in their mixtures, theory cannot be used to accurately predict flic resulting vapor pressure. [Pg.51]

Acrylic acid is a moderately strong carboxylic acid. Its dissociation constant is 5.5 x 10. Vapor pressure as a function of temperature is given in Table 4 for acrylic acid and four important esters (4,16—18). The lower esters form a2eotropes both with water and with their corresponding alcohols. [Pg.150]

Primary human skin irritation of tetradecanol, hexadecanol, and octadecanol is nil they have been used for many years ia cosmetic creams and ointments (24). Based on human testing and iudustrial experience, the linear, even carbon number alcohols of 6—18 carbon atoms are not human skin sensitizers, nor are the 7-, 9- and 11-carbon alcohols and 2-ethylhexanol. Neither has iudustrial handling of other branched alcohols led to skin problems. Inhalation hazard, further mitigated by the low vapor pressure of these alcohols, is slight. Sustained breathing of alcohol vapor or mist should be avoided, however, as aspiration hazards have been reported (25). [Pg.446]

RVP is a vapor pressure measurement at a fixed air/Hquid ratio of 4 and a temperature of 38°C. It is measured under conditions of water saturation. For samples which contain water-soluble components such as alcohols, ASTM D4953 is used. [Pg.182]

Tetrahydronaphthalene [119-64-2] (Tetralin) is a water-white Hquid that is insoluble in water, slightly soluble in methyl alcohol, and completely soluble in other monohydric alcohols, ethyl ether, and most other organic solvents. It is a powerhil solvent for oils, resins, waxes, mbber, asphalt, and aromatic hydrocarbons, eg, naphthalene and anthracene. Its high flash point and low vapor pressure make it usehil in the manufacture of paints, lacquers, and varnishes for cleaning printing ink from rollers and type in the manufacture of shoe creams and floor waxes as a solvent in the textile industry and for the removal of naphthalene deposits in gas-distribution systems (25). The commercial product typically has a tetrahydronaphthalene content of >97 wt%, with some decahydronaphthalene and naphthalene as the principal impurities. [Pg.483]

The physical characteristics of /i /f-amyl alcohol diverge from the standard trends for the other alcohols it has a lower boiling point, higher melting point, higher vapor pressure, and low surface tension. Most notably, organic molecules are highly soluble in /i /f-amyl alcohol. [Pg.372]

Physical and chemical properties of isopropyl alcohol reflect its secondary hydroxyl functionaHty. For example, its boiling and flash poiats are lower than / -propyl alcohol [71-25-8], whereas its vapor pressure and freezing poiat are significantly higher. Isopropyl alcohol bods only 4°C higher than ethyl alcohol. [Pg.104]

The most common a2eotropes (3,4) formed by the butanols are given in Table 2. Butyl alcohol Hquid vapor pressure/temperature responses (5,6), which are important parameters in direct solvent appHcations, are presented in Figure 1. Similarly, viscosity/temperature plots (1) for the four butanols are presented in Figure 2. [Pg.356]

Fig. 1. Vapor pressure of butyl alcohols A, n-hutyV, B, isobutyl C, j -butyl D, /-butyl. To convert kPa to mm Hg, multiply by 7.5. Fig. 1. Vapor pressure of butyl alcohols A, n-hutyV, B, isobutyl C, j -butyl D, /-butyl. To convert kPa to mm Hg, multiply by 7.5.
A summary of physical properties of ethyl alcohol is presented ia Table 1. Detailed information on the vapor pressure, density, and viscosity of ethanol can be obtained from References 6—14. A listing of selected biaary and ternary azeotropes of ethanol is compiled ia Reference 15. [Pg.401]

Toluene is a notoriously poor electrical conductor even in grounded equipment it has caused several fires and explosions from static electricity. Near normal room temperature it has a concentration that is one of the easiest to ignite and, as previously discussed, that generates maximum explosion effects when ignited (Bodurtha, 1980, p. 39). Methyl alcohol has similar characteristics, but it is less prone to ignition by static electricity because it is a good conductor. Acetone is also a good conductor, but it has an equihbrium vapor pressure near normal room temperature, well above UFL. Thus, acetone is not flammable in these circumstances. [Pg.2317]

Aldehydes and Ketones — These share many chemical properties because they possess the carbonyl (C=0) group as a common feature of their structure. Aldehydes and ketones have lower boiling points and higher vapor pressures than their alcohol counterparts. Aldehydes and ketones through C< are soluble in water and have pronounced odors. Ketones are relatively inert while aldehydes are easily oxidized to their counterpart organic acids. [Pg.170]

Low ambient temperatures resulting in subatmospheric vapor pressure of certain materials (e.g., some alcohols and aromatics) in pressure storage. [Pg.149]

Aero Hydrolysis. A solution of kasugamycin hydrochloride (1.5 grams, 3.46 mmoles) dissolved in 15 ml. of 6N hydrochloric acid was heated at 105°C. for five hours in a sealed tube. The solution was condensed to 5 ml. under a reduced pressure and the addition of 50 ml. of ethyl alcohol afforded a crude solid overnight. It was recrystallized from aqueous ethyl alcohol, showing m.p. 246°-247°C. (dec.). It showed no depression in the mixed-melting point and completely identical infrared spectrum with d-inositol which was supplied by L. Anderson of the University of Wisconsin. The yield was 81% (503 mg., 2.79 mmoles). Anal Calcd. for CgH12Og C, 40.00 H, 6.71 O, 53.29 mol. wt., 180.16. Found C, 40.11 H, 6.67 O, 53.33 mol. wt., 180 (vapor pressure osmometer). [Pg.40]

WEB Methyl alcohol, CH3OH, has a normal boiling point of 64.7°C and has a vapor pressure of203 mm Hg at 35°C. Estimate... [Pg.253]

Boiling point Temperature at which the vapor pressure of a liquid equals the applied pressure, leading to the formation of vapor bubbles, 13 alcohol, 591 alkane, 591 ether, 591... [Pg.683]

Ethyl alcohol is also a liquid at room temperature. Its vapor pressure at 20°C is 44 mm, higher than the vapor pressure of water at this same temperature. At 40°C, ethyl alcohol has a vapor pressure of 134 mm at 60°C, the vapor pressure is 352 mm. Again we find that the vapor pressure increases rapidly with increasing temperature. This is always so. The vapor pressure of every liquid increases as the temperature is raised. [Pg.67]

Consideration of the dissolving of iodine in an alcohol-water mixture on the molecular level reveals the dynamic nature of the equilibrium state. The same type of argument is applicable to vapor pressure. [Pg.145]

Gordon258 suggested orders 2 with respect to add and 1 with respect to alcohol for the reactions of adipic add with pentaerithrytol or with trimethylolpropane in bis(dioxa-3,6-heptyl ether) this reaction is followed by measuring the vapor pressure of the released water. [Pg.77]

Alcohols with low molar masses are liquids, and alcohols have much lower vapor pressures than do hydrocarbons with approximately the same molar mass. For example, ethanol is a liquid at room temperature, but butane, which has a higher molar mass than ethanol, is a gas. The relatively low volatility of alcohols is a sign of the strength of hydrogen bonds. The ability of alcohols to form hydrogen bonds also accounts for the solubility in water of alcohols with low molar mass. [Pg.875]


See other pages where Alcohols vapor pressure is mentioned: [Pg.839]    [Pg.839]    [Pg.190]    [Pg.115]    [Pg.48]    [Pg.424]    [Pg.87]    [Pg.88]    [Pg.75]    [Pg.459]    [Pg.241]    [Pg.552]    [Pg.373]    [Pg.368]    [Pg.48]    [Pg.501]    [Pg.475]    [Pg.2136]    [Pg.164]    [Pg.99]    [Pg.252]    [Pg.253]    [Pg.478]    [Pg.699]    [Pg.67]    [Pg.69]    [Pg.322]    [Pg.1029]   
See also in sourсe #XX -- [ Pg.7 ]

See also in sourсe #XX -- [ Pg.7 ]




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