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Alcohol distribution

Fig. 2. Estimated primary alcohol distributions for (H) Ethyl Corporation-modified Ziegler and (+) Vista Corporation Ziegler, at 4.0 moles ethylene per... Fig. 2. Estimated primary alcohol distributions for (H) Ethyl Corporation-modified Ziegler and (+) Vista Corporation Ziegler, at 4.0 moles ethylene per...
FIGURE 9.21 Alcohol distributions at different pressures of FT synthesis on cobalt. Further legend as in Figure 9.18. [Pg.178]

Most of the alcohol distributes into body water, but like most solvents and anesthetics some distributes into fat. It is excreted in the urine and breath, hence the utility of taking breath samples to evaluate alcohol exposure. The majority of alcohol is metabolized in the liver. Alcohol dehydrogenase (ADH) metabolizes alcohol to acetaldehyde. Acetaldehyde is toxic, with elevated levels causing flushing, headache, nausea, and vomiting. Acetaldehyde is in turn quickly metabolized to the less toxic acetate by acetaldehyde dehydrogenase (ALDH) (Figure 3.1). [Pg.42]

Sulfided and alkalinizeS molybdenum based catalysts have recently been claimed (14,15) mixed Mo(Co)K sulfides yield similar alcohol distributions under substoichiometric syngas and H S (0.05-0.1 vol %)y (16,17). ... [Pg.43]

Hydroxylation of alkanes can be performed by TBHP or cumyl hydroperoxide in the presence of iron porphyrin catalysts.S0 502 The characteristics of this reaction are very different from PhIO/Fe(TPP) systems. No epoxidation of alkenes occurs, and the alcohol distribution is completely independent of the nature of the iron porphyrin used (equation 228). A Fenton-type mechanism involving active species not including the metal has been suggested (equation 229). [Pg.383]

The one-compartment model of distribution assumes that an administered drug is homogeneously distributed throughout the tissue fluids of the body. For instance, ethyl alcohol distributes uniformly throughout the body, and therefore any body fluid may be used to assess its concentration. The two-compartment model of distribution involves two or multiple central or peripheral compartments. The central compartment includes the blood and extracellular fluid volumes of the highly perfused organs (i.e., the brain, heart, liver, and kidney, which receive three fourths of the cardiac output) the peripheral compartment consists of relatively less perfused tissues such as muscle, skin, and fat deposits. When distributive equilibrium has occurred completely, the concentration of drug in the body will be uniform. [Pg.12]

Ethyl s version of the Ziegler alcohol process has been modified in order to control the product alcohol distribution. Whereas the Conoco ALFOL alcohol process affords the full range of alcohols, C2-C3o, in a Poisson distribution, Ethyl s product distribution can be modified, for example, as shown in Figure 3 to give carbon number distributions to fit the needs of the market. [Pg.100]

Colonial powers divested Chinese merchants of control of many trading monopolies granted by the precolonial local authorities, hut left them in control of gambling and local drug and alcohol distribution because Chinese secret societies were uniquely... [Pg.87]

Alcohol distributes into the aqueous compartments of blood, and because the water content of serum ( 98%) is greater than that of whole blood ( 86%), results indicating higher alcohol levels are obtained with serum. Experimentally the serum whole blood ethanol ratio is 1.14 (1.09 to 1,18) and varies slightly with hematocrit.Several states have enacted laws that define intoxication while driving a motor vehicle under the influence of alcohol based on whole blood ethanol concentrations. Some states do not specify the specimen type. Therefore laboratories that perform alcohol determinations should make clear the choice of specimen. [Pg.1302]

Therefore, the inverse gas chromatography method allows us to determine the model of long-chain aliphatic alcohol distribution on the surface of porous silica gel if the amount of alcohol on adsorbent surface is equal or exceeds the monolayer capacity, then the monolayer is composed of alcohol molecules oriented their polar moieties to the adsorbent surface. The monolayer, in a solid-condensed state, is stable up to 81°C. At this temperature the monolayer transfers into a liquid-expanded state. The threedimensional excess of alcohol, because the autophobicity phenomenon, does not wet the monolayer surface. [Pg.507]

Two processes have been commerdalized on the basis of the oligomerization of ethylene, one by Conoco Chemical and the second by Ethyl Corporation. They differ in the distribution curve of the different alcohols formed. Whereas Conoco s Alfol alcohols range from C2 to C22 with about 55 per cent C12 or above (Fig. 9.S), the alcohol distribution of the Ethyl process is narrower and comprises 85 par cent C 2 - Tins change in the distribution curve results from the insertion of an additional stage of transalkylation by triisobutyUluminum. [Pg.97]

The classic experiments were those performed by Ernest Overton and Hans Meyer at the turn of the twentieth century, where tadpoles were placed in solutions containing alcohols of increasing hydrophobicity. They found a correlation between the concentration of the alcohol required to cause cessation of movement and the concentration of the alcohol distributed into the lipid phase of a lipid-water mixture. The ratio of the concentration in the lipid phase to the concentration in the aqueous phase at equilibrium is known as the Overton-Meyer or lipid-water partition coefficient. The higher the partition coefficient, the less alcohol was needed to cause cessation of movement. [Pg.51]

Figure 2 Alcohol distribution and stability curves (a) observed alcohols stabilities (arbitrary units) (b) observed alcohol distribution (c) suggested form of curve for initial distribution of alcohols, A) observed hydrocarbon distribution (literature data) (data from ref 44)... Figure 2 Alcohol distribution and stability curves (a) observed alcohols stabilities (arbitrary units) (b) observed alcohol distribution (c) suggested form of curve for initial distribution of alcohols, A) observed hydrocarbon distribution (literature data) (data from ref 44)...
Figure 12. Effect of carbon support type on alcohol distribution (320 °C, 300 psig, 3 Nl/g-cat/h, H2/CO = 0.9 48-72 h). Figure 12. Effect of carbon support type on alcohol distribution (320 °C, 300 psig, 3 Nl/g-cat/h, H2/CO = 0.9 48-72 h).
Partition constants report the equilibrium distribution of components in aggregated systems but do not represent the free energy of transfer of alcohols between aggregates and the bulk aqueous or oil phases, and their values need not be independent of solution composition, especially when the alcohol concentration in the aggregates or the bulk phase is high. However, alcohol distributions expressed as mass-action binding constants in aqueous three-component microemulsions [reaction (16)] and in W/O microemulsions [reaction (17)] are independent of alcohol concentration. [Pg.476]

Ahphatic hydrocarbons and other nonpolar compounds are thought to be incorporated or solubilized in the micelle interiors (Figure 4.22a). Molecules having some surface activity, such as alcohols, distribute themselves among the surfactant molecules, as shown in Figure 4.22b. This simation is closely related to formation of micelles from mixtures of surfactants, which was discussed previously. Rather polar substances may even occupy positions at the micelle surface (Figure 4.22c). [Pg.202]

The effect of water-to-oil ratio By increasing the overall water-to-oil ratio in a given system, with everything else being kept constant, the alcohol content in each phase can either decrease or increase, depending on the alcohol distribution between hydrocarbon and water. If the partition coefficient, defined as the alcohol concentration in the oil phase divided by its concentration in the aqueous phase, is less than one, an increase in the WOR induces a decrease in the alcohol concentration in both phases. This is the case with isopropanol and the water-octane pair. This is pointed out elsewhere (6). [Pg.121]

Elhoxylated alcohol distributions from 2 to 40 ethylene oxide units (e.g., Brij 76) were characterized on a diol phase (ELSD) using a 25-min 90/10->20/80 hexane/(98/2 chloroform/IPA) gradient [645]. Good separation throughout the homologous series resulted. Peak shapes were acceptable as well. Tables of retention times for hexadecylalcohol-ethoxylated compounds (1-6 ethoxy groups) and for Cio-Cig hexaethoxylated alcohols were presented. [Pg.237]

The distribution coefficient of alcohol between water and CCl is 40.98. How will Ig of alcohol distribute itself between 20 cm of water and 50 cm of CCL. 4 16. At 293 K, SOj was permitted to distribute itself between 0.2 dm of CHCIj and 0.075 dm of water. When equilibrium was established the CHCI3 layer contained 0.14 mole of SOj and the water layer 0.05 mole. Calculate the distribution coefficient at this temperature. ... [Pg.230]

Table 2. Long chain fatty alcohol distribution (LCFA) of sorghum blades during plant maturation. Table 2. Long chain fatty alcohol distribution (LCFA) of sorghum blades during plant maturation.

See other pages where Alcohol distribution is mentioned: [Pg.179]    [Pg.179]    [Pg.301]    [Pg.101]    [Pg.218]    [Pg.278]    [Pg.784]    [Pg.50]    [Pg.610]    [Pg.51]    [Pg.110]    [Pg.97]    [Pg.133]    [Pg.133]    [Pg.138]    [Pg.475]    [Pg.475]    [Pg.476]    [Pg.134]    [Pg.692]    [Pg.30]    [Pg.247]    [Pg.493]    [Pg.493]    [Pg.168]   
See also in sourсe #XX -- [ Pg.196 ]




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