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Ethanol mixtures

Structural birth defects Abnormal facial features Growth problems [Pg.409]

CNS problems Difficulty learning Memory problems Vision problems Hearing problems Behavioral problems [Pg.410]

Mixtures of ethanol with other toxic chemicals produce unanticipated effects with greater teratogenic effects than ethanol or its mixture partners alone. The following study illustrates this phenomenon. [Pg.410]

Polluted air is a postnatal developmental problem as well as a prenatal one. Studies in California have demonstrated that exposure to polluted air impairs lung development and lung function in children and young adults. I35-37  [Pg.410]

A study in the Netherlands reported congenital malformations in the offspring of male painters with occupational exposure to organic solvents. I38 [Pg.410]


In spite of their easy interconversion in solution a and p forms of carbohydrates are capable of independent existence and many have been isolated m pure form as crys talline solids When crystallized from ethanol d glucose yields a d glucopyranose mp 146°C [a]o +112 2° Crystallization from a water-ethanol mixture produces p d glucopyranose mp 148-155°C [aj +18 7° In the solid state the two forms do not mterconvert and are stable indefinitely Their structures have been unambiguously con firmed by X ray crystallography... [Pg.1040]

BBT solution on unmodified sorbents of different nature was studied. Silica gel Merck 60 (SG) was chosen for further investigations. BBT immobilization on SG was realized by adsoi ption from chloroform-hexane solution (1 10) in batch mode. The isotherm of BBT adsoi ption can be referred to H3-type. Interaction of Co(II), Cu(II), Cd(II), Ni(II), Zn(II) ions with immobilized BBT has been studied in batch mode as a function of pH of solution, time of phase contact and concentration of metals in solution. In the presence of sodium citrate absorbance (at X = 620 nm) of immobilized BBT grows with the increase of Cd(II) concentration in solution. No interference was observed from Zn(II), Pb(II), Cu(II), Ni(II), Co(II) and macrocomponents of natural waters. This was assumed as a basis of soi ption-spectroscopic and visual test determination of Cd(II). Heavy metals eluted from BBT-SG easily and quantitatively with a small volume of HNO -ethanol mixture. This became a basis of soi ption-atomic-absoi ption determination of the total concentration of heavy metals in natural objects. [Pg.292]

The molecular weight may be regulated by controlled degradation of the alkali cellulose in the presence of air. This can be done either before or during etherification. The molecular weight of commercial grades is usually expressed indirectly as viscosity of a 5% solution in an 80 20 toluene-ethanol mixture. [Pg.630]

The d5-l,2-cyclodecanediol will have crystallized out of solution, while the trans-Aio remains in the ethanol. The entire mixture is washed out of the bomb with 95% ethanol (about 11.). The cis-glycol is redissolved by heating the ethanolic mixture at reflux temperature. Filter aid ( Celite ) is added to the mixture, and the hot mixture is filtered through a bed of filter aid on a Buchner funnel to remove the catalyst. The ethanol is... [Pg.12]

Scott and Beesley [2] measured the corrected retention volumes of the enantiomers of 4-benzyl-2-oxazolidinone employing hexane/ethanol mixtures as the mobile phase and correlated the corrected retention volume of each isomer to the reciprocal of the volume fraction of ethanol. The results they obtained at 25°C are shown in Figure 8. It is seen that the correlation is excellent and was equally so for four other temperatures that were examined. From the same experiments carried out at different absolute temperatures (T) and at different volume fractions of ethanol (c), the effect of temperature and mobile composition was identified using the equation for the free energy of distribution and the reciprocal relationship between the solvent composition and retention. [Pg.158]

FIG. 5 Local concentration profiles around a hydroxyl group in poly(vinyl alcohol) of heavy atoms in a (1 1) water/ethanol mixture A = OW water oxygen, A = OE ethanol oxygen, A = CE ethanol carbon. The local atomic fractions are defined as = a( )/ ZIb where a( ) is average number of atoms... [Pg.494]

In spite of theii easy interconversion in solution, a and p fonns of carbohydrates are capable of independent existence, and many have been isolated in pure fonn as crystalline solids. When crystallized from ethanol, D-glucose yields a-D-glucopyianose, mp 146°C, [a]o -1-112.2°. Crystallization from a water-ethanol mixture produces P-d-glucopyranose, mp 148-155°C, +18.7°. In the solid state the two fonns do not... [Pg.1040]

Addition of co-solvents can also change the co-miscibility characteristics of ionic liquids. As an example, the hydrophobic [BMIM][PFg] salt can be completely dissolved in an aqueous ethanol mixture containing between 0.5 and 0.9 mole fraction of ethanol, whereas the ionic liquid itself is only partially miscible with pure water or pure ethanol [13]. The mixing of different salts can also result in systems with modified properties (e.g., conductivity, melting point). [Pg.262]

A sample of polyester (ca. 1 g, exactly weighed) is dissolved in 20 mL toluene-ethanol mixture (1/1 vol.) and titrated by a solution of KOH in ethanol (0.05 mol/L) using a potentiometric titrator. A blank titration must be performed under the same conditions. Hardly soluble polyesters (e.g., PET) must be dissolved in an o-cresol-chloroform mixture or in hot benzyl alcohol.417 The result (acid content) is normally expressed in mmol COOH/g polyester but may also be given as the acid number, defined as the number of milligrams of KOH required to neutralize 1 g of polyester. [Acid number = (number of mmol COOH/g polyester) x 56.106.]... [Pg.94]

By extraction of animal lymph glands, parotid glands, pancreas, liver, milt and blood serum with diluted acetic acid-ethanol-mixtures upon removal of fat and proteins. [Pg.134]

Photocatalytic dehydrogenation in the presence of heteropolyacids. Upon illumination with the UV quanta, heteropolyacid H4[SiW]204o] provides with the quantum yield cp = 0.2 (at X = 333 nm) and remarkable (ca. 100%) selectivity dehydrogenation of ethanol into acetaldehyde in water-ethanol mixtures [10] ... [Pg.36]

A 95/5 nitric acid/ethanol mixture made in error (instead of 5/95) caused it to explode. [Pg.150]

S-methyldithiocarbazates of 2-formylquinoline, 18, and 1-formylisoquinoline, 19, have been found to act as anionic tridentate ligands with iron(III) forming [FeLj] [FeC ] on isolation from a dimethoxypropane-ethanol mixture [145]. No new spectral data was provided when [Fe(19-Fl)2] [FeCl4] was included in a more recent paper [146],... [Pg.18]

BTEX-ethanol mixtures through bioaugmentation, in Situ and On-Site Bioremediation Conference, Orlando, FL, June 2, 2003. [Pg.1053]

For the preparation of methyl orthoformate, solid sodium methoxide, methanol and chloroform were mixed together. The mixture boiled violently and then exploded [1]. The analogous preparation of ethyl orthoformate [2] involves the slow addition of sodium or sodium ethoxide solution to a chloroform-ethanol mixture. The explosion was caused by the addition of the solid sodium methoxide as one portion. See Sodium, etc., above... [Pg.151]

Treatment of 220 with benzylidenemalononitrile in a DMF/ethanol mixture under basic conditions affords 1 1 adduct 221 in 69% yield (Equation 31) <2005HC089>. [Pg.401]

A good catalyst for this reaction is [FeH(CO)4], produced by the reaction of [Fe(CO)5] with OH-.348 Aldehydes were reduced by CO in 60 40 water 2-ethoxy-ethanol mixtures under mild condition (30-80 °C, 20 bar CO) with a [Rh6(CO)16]/diamine catalyst system.349 In aqueous... [Pg.121]

Wash the substrate several times with ethanol or the water/ethanol mixture to remove excess silane compound. [Pg.566]

The relative remaining activity of alcohol dehydrogenase in an optimal water-ethanol mixture exceeded 100%. The observation of the improved activity of some of the enzyme samples after this procedure [179] was a precursor to later achievements on enzyme activation in organic media [178],... [Pg.451]

E.V. Kudryashova, A.K. Gladilin, A.V. Vakurov, F. Heitz, A.V. Levashov, and V.V. Mozhaev, Enzyme-poly electrolyte complexes in water-ethanol mixtures negatively charged groups artificially introduced into alpha-chymotrypsin provide additional activation and stabilization effects. Biotechnol. Bioeng. 55, 267-277 (1997). [Pg.461]

Bennet, D., Canady, J. (1984) Thermodynamics of solution of naphthalene in various water-ethanol mixtures. J. Am. Chem. Soc. 106, 910-915. [Pg.901]

In the OFRR, the wall thickness is important, as it determines the fraction of the light in the core that interacts evanescently with the gain medium when the solvent is of low RI. To precisely characterize the OFRR thickness noninvasively, we use the method developed previously22, in which various concentrations of water-ethanol mixtures are passed through the OFRR, and the WGM spectral shift in response to RI changes in the core is plotted as demonstrated in Fig. 19.4b. By matching the experimental sensitivity results with those obtained from our... [Pg.518]

Absolute (100%) ethanol is often made by adding benzene to the ethanol -water binary azeotrope (two components), to make a ternary azeotrope (three components). This ternary alcohol-water-benzene (18.5 7.4 74.1) azeotrope comes over until all the water is gone, followed by a benzene-ethanol mixture. Finally, absolute ethanol gets its chance to appear, marred only slightly by traces of benzene. [Pg.307]

Rates of the Rh(m) complex were highest in water-ethanol mixtures of a 22 3 ratio. Rate dependence data, provided in Table 21, suggested the metallo-carboxylic acid mechanism (not unlike that of Darensbourg,61 Scheme 20 or Tanaka,75 Scheme 27) depicted in Scheme 37, and the kinetic equation in the lower pH region where Pco >0.3 atm was found to be ... [Pg.154]


See other pages where Ethanol mixtures is mentioned: [Pg.433]    [Pg.45]    [Pg.108]    [Pg.1248]    [Pg.22]    [Pg.143]    [Pg.157]    [Pg.493]    [Pg.112]    [Pg.911]    [Pg.438]    [Pg.678]    [Pg.223]    [Pg.323]    [Pg.5]    [Pg.37]    [Pg.845]    [Pg.95]    [Pg.348]    [Pg.376]    [Pg.186]    [Pg.241]    [Pg.162]    [Pg.261]    [Pg.1416]    [Pg.1421]    [Pg.131]   
See also in sourсe #XX -- [ Pg.173 ]




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Calculation aqueous ethanol mixtures

DMSO/ethanol mixtures

Dehydration of aqueous ethanol mixtures

Density ethanol-water mixtures

Density of Ethanol-Water Mixtures

Distillation of aqueous ethanol mixtures

Ethanol methanol mixtures

Ethanol siloxane mixtures

Ethanol-methanol-water mixtures

Ethanol-water mixtures

Ethanol-water mixtures ternary azeotropes

Ethanol-water mixtures, freezing point

Ethanol-water mixtures, physicochemical

Ethanol-water mixtures, properties

Ethanol-water mixtures, separation

Ethanol-water-toluene mixture

Ethanol/water mixture, azeotropes

Ethanol/water mixture, fractional

Ethanol/water/toluene mixture, azeotropes

Ethyl-acetate-ethanol-water mixture

Mechanisms of Ethanol Mixture Toxicity

Pervaporation ethanol/water mixture

Water-ethanol mixture, mole fraction

Water-ethanol mixtures preferential solvation

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