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Fermentation ethyl alcohol

Fusel Oils. The original source of amyl alcohols was from fusel oil which is a by-product of the ethyl alcohol fermentation industry. Refined amyl alcohol from this source, after chemical treatment and distillation, contains about 85% 3-methyl-1-butanol and about 15% 2-methyl-1-butanol, both primary amyl alcohols. Only minor quantities of amyl alcohol are suppHed from this source today. A German patent discloses a distillative separation process for recovering 3-methyl-1-butanol from fusel oil (93). [Pg.373]

The ethyl alcohol fermentation is of course an age-old process and is so well known that little need be said about it here. The acetone-butanol fermentation is perhaps the next most important industrial fermentation process, although starch in the form of maize has been largely used as the basic material more recently suitably treated molasses has been used. The fermentation, a relatively rapid process requiring about thirty hours, produces about 60 parts of butanol, 30 parts of acetone and 10 parts of ethyl alcohol. These products already have large uses in industry and other uses are being explored. One possibility is the use of butanol in motor fuel. Jean has described a fuel, called Jeanite, consisting mainly of butanol and ethyl alcohol, which shows some promise. Of course the admixture of ethyl alcohol with petroleum is well known and an increased use of this mixture is probable. [Pg.323]

The catalytic action of living organisms, or rather of the proteins they contain, had received the beginnings of an explanation with the experiments of Payen and Persoz on malt amylase separation in 1833 and with J. J, Berzelius s catalyst theory in 1835. In 1897 Eduard Buchner demonstrated that a yeast extract could turn sucrose into ethyl alcohol, Fermentation took place without the presence of living organisms through enzymes. In this case zymase was the catalyst. [Pg.16]

As a beverage ethanol had been prepared and used long ago by the Egyptian pharaohs (2,3). Some iadication of the antiquity of the knowledge of ethyl alcohol is the fact that Noah is beheved to have built a vineyard ia which he grew grapes that he fermented iato a type of alcohoHc beverage (4). [Pg.401]

Industrial ethyl alcohol can be produced synthetically from ethylene [74-85-17, as a by-product of certain industrial operations, or by the fermentation of sugar, starch, or cellulose. The synthetic route suppHes most of the industrial market in the United States. The first synthesis of ethanol from ethylene occurred in 1828 in Michael Faraday s lab in Cambridge (40). [Pg.403]

Nature produces a tremendous amount of methyl aleohol, simply by the fermentation of wood, grass, and other materials made to some degree of eellulose. In faet, methyl aleohol is known as wood aleohol, along with names sueh as wood spirits and methanol (its proper name the proper names of all aleohols end in -ol). Methyl aleohol is a eolorless liquid with a eharaeteristie aleohol odor. It has a flash point of 54°F, and is highly toxie. It has too many eommereial uses to list here, but among them are as a denaturant for ethyl alcohol (the addition of the toxie ehemieal methyl aleohol to ethyl aleohol in order to form denatured aleohol), antifreezes, gasoline additives, and solvents. No further substitution of hydroxyl radieals is performed on methyl aleohol. [Pg.198]

It can be obtained by the oxidation of ethyl alcohol, either chemically or by fermentation under the influence of the organised ferment Myco-dernia aceti. [Pg.295]

Gknings-alkohol, m. ethyl alcohol, -amylal-kohol, m. amyl alcohol of fermentation (a mixture of 2- and 3- methylbutanol). -but-tersaure,/. (ordinary) butyric acid, -chemie, /. fermentation chemistry, zymurgy. [Pg.170]

In some parts of the world, as in Russia, fermented alcohol can serve as a cheap source for hutadiene. The reaction occurs in the vapor phase under normal or reduced pressures over a zinc oxide/alumina or magnesia catalyst promoted with chromium or cohalt. Acetaldehyde has been suggested as an intermediate two moles of acetaldehyde condense and form crotonaldehyde, which reacts with ethyl alcohol to give butadiene and acetaldehyde. [Pg.104]

Ethyl alcohol (CH3CH2OH) production is considered by many to be the world s oldest profession. Fermenting carbohydrates is still the... [Pg.204]

Synthetic ethyl alcohol (known as ethanol to differentiate it from fermentation alcohol) was originally produced hy the indirect hydration of ethylene in the presence of concentrated sulfuric acid. The formed mono-and diethyl sulfates are hydrolyzed with water to ethanol and sulfuric acid, which is regenerated ... [Pg.205]

Glucose, C6Hi206(s), (AH = —1275.2 kj/mol) is converted to ethyl alcohol, CjHsOHt/), and carbon dioxide in die fermentation of grape juice. What quantity of heat is liberated when 750.0 mL of wine containing 12.0% ethyl alcohol by volume (d = 0.789 g/cm3) is produced by the fermentation of grape juice ... [Pg.223]

The wine in the goblet can be produced by the fermentation of glucose (present in all the fruits shown in the painting) to ethyl alcohol. [Pg.578]

The puipose of the bubble chamber in the fermentation jug (center) is to allow the carbon dioxide to escape but prevent oxygen from entering and oxidizing ethyl alcohol to acetic acid. [Pg.592]

In fermentation for the production of acetic acid, ethyl alcohol is used in an aerobic process. In an ethanol oxidation process, the biocatalyst Acetobacter aceti was used to convert ethanol to acetic acid under aerobic conditions. A continuous fermentation for vinegar production was proposed for utilisation of non-viable A. aceti immobilised on the surface of alginate beads. [Pg.238]

C04-0062. The fermentation of sugar to produce ethyl alcohol occurs by the following reaction yeast... [Pg.263]

The qualification for nature identical varies between jurisdictions. In the EU, ethyl acetate made from fermented ethyl alcohol and fermented acetic acid is nature identical. In the USA, provided that the ethyl alcohol and acetic acid are natural, i.e. produced by fermentation, the ethyl acetate would be natural. [Pg.100]

Fermenting grains with yeast produces a grain alcohol. The process also works with other biomass feedstocks. In fermentation, the yeast decomposes carbohydrates which are starches in grains, or sugar from sugar cane juice into ethyl alcohol (ethanol) and carbon dioxide. The process breaks down complex substances into simpler ones. [Pg.93]

The conversion of ethyl alcohol by way of acetaldehyde into acetic acid is the chemical expression equivalent to acetic fermentation. In this process the acetic bacteria utilise atmospheric oxygen in order to bind the hydrogen. That the hydrogen which has to be removed is activated, and not the oxygen (as was formerly thought), is shown by experiments in which oxygen is eaxluded and replaced by quinone the bacteria produce acetic acid from alcohol as before and the quinone is reduced to hydroquinone. [Pg.212]

Uses. Nearly half the ethyl alcohol produced in petrochemical plants (not the stuff fermented for human consumption) is used as a chemical intermediate in the manufacture of ethyl acrylate, ethyl amines, ethyl acetate (when you pop the cap on nail polish remover, you smell ethyl acetate), ethylene chloride, glycol ethers, acetaldehyde, and acetic acid. However, you will see in the chapters on acetaldehyde and acetic acid, there are now more competitive routes than those based on ethyl alcohol. [Pg.197]

Approximately 2.6 gallons of ethyl alcohol (95% ethyl alcohol and 5% water) are produced per bushel of corn. Fermentation costs about 50 cents per gallon of ethyl alcohof and corn is selling for about 2.50 per bushel. If the operating costs of an ethyl alcohol plant are 30 cents per gallon, what is the maximum price that could be paid for ethylene to remain competitive with natural ethyl alcohol ... [Pg.212]


See other pages where Fermentation ethyl alcohol is mentioned: [Pg.636]    [Pg.637]    [Pg.557]    [Pg.562]    [Pg.573]    [Pg.578]    [Pg.636]    [Pg.637]    [Pg.557]    [Pg.562]    [Pg.573]    [Pg.578]    [Pg.407]    [Pg.408]    [Pg.83]    [Pg.20]    [Pg.401]    [Pg.412]    [Pg.324]    [Pg.738]    [Pg.594]    [Pg.239]    [Pg.62]    [Pg.506]    [Pg.120]    [Pg.89]    [Pg.160]    [Pg.138]    [Pg.194]    [Pg.194]    [Pg.198]   


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