Ethanol INDEX

As an example, the battery-limits capital cost can be estimated for the production of 10,000 t/yr of ethylene (qv) from ethanol (11). Seven processing blocks, ie, vaporizer, reactor, water quench, compressor, dryer, distillation, and energy recovery, can be identified. The highest temperature is 350°C (reactor), and the highest pressure is about 1.7 MPa (17 atm) (compressor, two towers). If a materials-pressure factor, + of 1.03 is assumed, then for N = 7 0 = 0.87 1/0 = 1 64 and f =0 K = 6.3. This gives the 1981 cost as 4.4 X 10 . The 1991 battery-Hmits investment can be obtained, by updating with the CE Plant Cost Index, as 5.3 x 10 . ... 

Ethyl Vinyl Ether. The addition of ethanol to acetylene gives ethyl vinyl ether [104-92-2] (351—355). The vapor-phase reaction is generally mn at 1.38—2.07 MPa (13.6—20.4 atm) and temperatures of 160—180°C with alkaline catalysts such as potassium hydroxide and potassium ethoxide. High molecular weight polymers of ethyl vinyl ether are used for pressure-sensitive adhesives, viscosity-index improvers, coatings and films lower molecular weight polymers are plasticizers and resin modifiers. 

The tartrate salt is recrystallized by dissolving in hot methanol, filtering, adding hot ethanol to the filtrate and cooling. The product is collected and air-dried. MP 148°-150°C. A second crop is obtained from the filtrate for a total yield of 59%. The tartrate is then metathe-sized with pamoic acid (Merck Index 6867) to give pyrantel pamoate as the product. 

Refractive Index is used to analyse the sample. It can also be used to help determine the percentage of a chemical (such as ethanol) in an aqueous solution. Refractive index (RI) is always reported to four decimal places. An example of the RI scale is shown in Figure 10.4. The correct reading from the RI of the sample would be 1.3764. 

The free oil can be determined by an ion exchange HPLC technique. A solution of the sample in ethyl alcohol is analysed by high-performance ion exchange chromatography using a specially prepared ion exchange resin stationary phase, ethanol mobile phase, and differential refractive index detection. 

Chang SC, Leung LWH, Weaver MJ. 1990. Metal crystallinity effects in electrocatalysis as prohed hy real-time ETIR spectroscopy electrooxidation of formic acid, methanol, and ethanol on ordered low-index platinum surfaces. J Phys Chem 94 6013-6021. 

Xia XH, Liess HD, Iwasita T. 1997. Early stages in the oxidation of ethanol at low index single crystal platinum electrodes. J Electroanal Chem 437 233-240. 

However, not withstanding the above objections, further discussion of the Snyder solvent triangle classification method is justified by its common use in many solvent optimization schemes in liquid chromatography. The polarity index, P, is given by the sum of the logarithms of the polar distribution constants for ethanol, dioxane and nltromethane and the selectivity parameters, X, as the ratio of the polar distribution constant for solute i to... 

The solvent triangle classification method of Snyder Is the most cosDBon approach to solvent characterization used by chromatographers (510,517). The solvent polarity index, P, and solvent selectivity factors, X), which characterize the relative importemce of orientation and proton donor/acceptor interactions to the total polarity, were based on Rohrscbneider s compilation of experimental gas-liquid distribution constants for a number of test solutes in 75 common, volatile solvents. Snyder chose the solutes nitromethane, ethanol and dloxane as probes for a solvent s capacity for orientation, proton acceptor and proton donor capacity, respectively. The influence of solute molecular size, solute/solvent dispersion interactions, and solute/solvent induction interactions as a result of solvent polarizability were subtracted from the experimental distribution constants first multiplying the experimental distribution constant by the solvent molar volume and thm referencing this quantity to the value calculated for a hypothetical n-alkane with a molar volume identical to the test solute. Each value was then corrected empirically to give a value of zero for the polar distribution constant of the test solutes for saturated hydrocarbon solvents. These residual, values were supposed to arise from inductive and... 

Products were analyzed via Waters Model 515 HPLC Pump fitted with a Waters model 2410 refractive index detector. Separations was performed via an Aminex HP-87H 300mm column at 65°C using 0.005M H2SO4 as the mobile phase. Compounds calibrated for this work included xylitol, arabitol, erythritol, threitol, PG, EG, glycerol, lactate, 1-propanol, 2-propanol, ethanol, methanol, and the butanetriol isomers. Any compounds not visible by RID were not quantified in this work. 

The Merck Index (12) gives the solubility in water as 30.1 mg per ml at 15°C, and kk.2 mg per ml at 258C. In 35% ethanol, the solubility is given as 2 mg per ml. These are consistent with the following approximate solubility data, determined at room temperature ... 

Use of refractive index for quantitative measurements requires careful temperature control. Change of temperature by 1°C can result in a decrease in refractive index of 0.0002-0.0004 for aqueous solutions. Solutions of ethanol can see a decrease in refractive index of as much as 0.0008°C ... 

Iogen (2005). Cellulose Ethanol Demonstration Facility, www.iogen.ca/company/ facilities/index.html. 

In Eq. (88), dn0/dl expresses how the refractive index % of the binary solvent alone varies with its composition expressed as volume fraction 4>y of liquid-1. Clearly, if liquids 1 and 3 are iso-refractive or nearly so, then M = M2, that is, a LS experiment will yield the true molecular weight irrespective of the composition of the mixed solvent. This situation is exemplified133) by the system polystyrene -ethyl-acetate (l)-ethanol (3) for which the molecular weight in mixed solvents of different 0i is the same as that obtained in pure ethylacetate (Fig. 40). The values of dn /d0j for the mixed solvents are only of the very small order of ca. 0.01, whilst the values of dn/dc for the polymer solutions are large (ca. 0.22 ml/g). 

Hj Dj exchange on, 26 39-43 heteropolyanion-supported, 41 230-231 high MiUer index, 26 12-15,35,36 -H-USY zeoUte, 39 186-187 hydrocarbons adsorption, 38 229-230 reactions of cyclopropane, cyclohexane, and n-heptane, 26 51-53 structural effects, 30 25-26 hydrogen adsorption on, 23 15 hydrogenation, 30 281-282 olefins, in ethanol, 30 352-353 in hydrogenation reaction, 33 101 -iron alloys, 26 75 isomerization, 30 2-3 isotope, NMR properties, 33 213,274 kinetic oscillations, 37 220-228 ball models of densely packed surfaces, 37 221-222... 

Many CNS depressants have some liability for dependence. This is typically greater with barbiturates, but lesser with benzodiazepines, and perhaps nonexistent in many antiseizure medications. CNS depressants produce tolerance when administered chronically, where increasingly larger doses are required to sustain the same level of effect. Further, a cross-tolerance often develops, where the tolerance is generalized to other CNS depressants. For example, a person with an ethanol tolerance will also display some tolerance to barbiturates. The therapeutic index tends to decrease as tolerance increases, so that the difference between an effective and toxic dose diminishes. Thus, tolerance to CNS depressants is accompanied by a smaller safety margin. 

It crystallizes from ethanol in two modifications which could not be separated from each other. Hence, a stmcture analysis from x-ray powder diffraction or even the indexing of the peaks turned out to be impossible. 

Aralaguppi, M.I., Jadar, C.V., and Aminabhavi, T.M. Density, viscosity, refractive index, and speed ofsound in binary mixtures of acrylonitrile with methanol, ethanol, propan-l-ol, butan-l-ol, pentan-l-ol, hexan-l-ol, heptan-l-ol, and butan-2-ol, J. 

Solubilities, in water, ethanol, and ethanol-water mixtures, have been reported for [Fe(phen)3]-(0104)2, [Fe(phen)3]2[Fe(CN)6], and [Fe(phen)3][Fe(phen)(CN)4]. Solubilities of salts of several iron(II) iiimine complexes have been measured in a range of binary aqueous solvent mixtures in order to estimate transfer chemical potentials and thus obtain quantitative data on solvation and an overall picture of how solvation is affected by the nature of the ligand and the nature of the mixed solvent medium. Table 8 acts as an index of reports of such data published since 1986 earlier data may be tracked through the references cited below Table 8, and through the review of the overall pattern for iron(II) and iron(III) complexes (cf. Figure 1 in Section 5.4.1.7 above) published recently. ... 

Monohydrate, Ba(0H)2 H20 is a white powder density 3.743 g/cm shght-ly soluble in water soluble in dilute mineral acids. Octahydrate, Ba(0H)2 8H20 is a colorless monoclinic crystal density 2.18 g/cm at 16°C refractive index 1.50 melts at 78°C vapor pressure 227 torr loses seven molecules of water of crystallization when its solution is boiled in the absence of atmospheric CO2 forming solid monohydrate further heating produces anhydrous Ba(OH)2 melting at 407°C readily dissolves in water (3.76 g/100 g at 20°C and 11.7 g/100 g at 50°C) aqueous solution highly aUtahne also soluble in methanol shghtly soluble in ethanol insoluble in acetone. 

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