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Dehydrated ethanol

Consider azeotropic distillation to dehydrate ethanol with benzene. Initial steady-state conditions are as shown in Fig. 13-108. The overhead vapor is condensed and cooled to 298 K to form two hquid phases that are separated in the decanter. The organic-rich phase is returned to the top tray as reflux together with a portion of the water-rich phase and makeup benzene. The other portion of the water-rich phase is sent to a stripper to recover organic compounds. Ordinarily, vapor from that stripper is condensed and recycled to the decanter, but that coupling is ignored here. [Pg.1343]

Under less-controlled conditions P4O10 dehydrates ethanol to ethene and methylai lcarbinols to the corresponding styrenes. H2SO4 is dehydrated to SO3, HNO3 gives N2O5 and amides... [Pg.505]

Ethanol. Ethanol is the most important chemical produced by fermentation, and it has the potential to become a major feedstock for the chemical industry since many other large-scale chemicals can be produced from ethanol. In fact, ethanol can in many respects be considered a renewable alternative to ethylene, which is the largest volume carbon-containing chemical produced from fossil resources today. Via catalytic dehydration, ethanol can easily be converted into ethylene and diethyl ether, both of which are well-known acid catalyzed processes. Almost all available... [Pg.25]

Tsao. U, Railly, J. W, Dehydrate ethanol to ethylene , Hydrocvbon Processing, 57 (2) 1 136 (1978). Farha, F. E, Banks, R. L, Triolefin process Chemistry and applications Petrochemical fotm-Americai Cor ressy Canqun, Mexico (12/18 Nov. 1978). [Pg.387]

Vumon Teniposide Bristol Myers Squibb Dimethylacetamide 6% Cremophor EL 50% Dehydrated ethanol 43% IV Infusion... [Pg.814]

Dehydrated ethanol Solubilizer, solubilizing agent, solvent iv, im, sc... [Pg.1634]

By the use of pressure and the proper catalysts it is possible to dehydrate ethanol to form butanol, 0 according to the reaction ... [Pg.228]

Crystals, mp 202-204 (dec). Freely sol in glacial acetic add sparingly sol in chloroform slightly sol in acetone, dehydrated ethanol, ethyl acetate, benzene. Practically insol in water. LDM in mice (g/kg) 3.3 orally > 2.0 i.p. (Kami -... [Pg.378]

A solution of 5.0 g. of shiny K in 72 ml. of carefully dehydrated ethanol is prepared in a round-bottom flask equipped with a reflux condenser and a drying tube. After the evolution of Hg ends, exactly half the solution is decanted and is saturated with HgS (in the absence of atmospheric moisture) in the manner described for NaHS. Excess HgS is removed by brief boilii in a stream of Ng or Hg. The two portions of the solution are then recombined in the original reaction flask. This K S solution is then mixed with 4.1 g. of pure S and boiled for 30 minutes orar e-yellow KgSg crystals separate. These are quickly suction-filtered in a fast Hg or Ng stream, washed with absolute ethanol, and freed of adhering solvent in a vacuum desiccator over PgOg. [Pg.364]

Spectral acquisition was performed on a Perkin Elmer Model Lambda 6 spectrophotometer using 1-cm quartz cells. The ultraviolet spectra of pergolide mesylate in water, methanol, and dehydrated ethanol are shown in Figure 7. UV absorption spectra of pergolide mesylate in water, methanol, and dehydrated ethanol exhibit different absorbances but similar spectral patterns. [Pg.397]

The measurement was perforni by adding an excess amount of sample to a solvent, shaking for thirty seconds at five-minute intervals for a total of diirty minutes, filtering the saturated solution, and determining the concentration of the drug in the filtered solution with a UVA IS spectrophotometer. (For dehydrated ethanol, ether, dimethylformamide, acetonitrile, dichloromethane, acetone, and chloroform, the filtered solutions were evaporated to dryness and reconstituted in methanol). [Pg.402]

Hydration- dehydration Ethanol s ethylene, also dehydration of higher alcohols Alumina phosphoric acid on a carrier... [Pg.79]

Although chloroform was widely used at one time for dehydrating ethanol, for which it is operationally well suited, its toxicity has caused it to be withdrawn from this use and from virtually any other application for which there is an acceptable alternative. [Pg.388]

This example involves vapor-liquid equilibrium (VLE) data for the design of a distillation tower to dehydrate ethanol. A portion of the T-x-y data for an ethanol-water mixture, measured at 1.013 bar (1 atm) using a Gillespie still (Rieder and Thompson, 1949), is shown in Figure 3.1a. Here, it is desired to use regression analysis to enable the UNIQUAC equation to represent the data accurately over the entire composition range. [Pg.64]

In creating your design, give special consideration to processes that reduce the energy expenditure of the plant. In one such process, pervaporation membranes are used to dehydrate ethanol. Pervaporation is a membrane separation process in which the feed and residue streams are liquid, but the permeate is a vapor. The combination of permeation and evaporation in the membrane gives rise to separation factors much greater than can be accomplished by distillation and can be used to break azeotropes. [Pg.946]


See other pages where Dehydrated ethanol is mentioned: [Pg.187]    [Pg.2194]    [Pg.730]    [Pg.384]    [Pg.210]    [Pg.45]    [Pg.58]    [Pg.379]    [Pg.605]    [Pg.214]    [Pg.52]    [Pg.1950]    [Pg.108]    [Pg.168]    [Pg.48]    [Pg.374]    [Pg.220]    [Pg.967]    [Pg.238]    [Pg.2445]    [Pg.2]    [Pg.24]    [Pg.2426]    [Pg.2198]    [Pg.397]    [Pg.402]    [Pg.191]    [Pg.178]    [Pg.245]    [Pg.45]    [Pg.189]   
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Ethanol dehydration

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