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Alcohol manufacturing process

Glyoxylic acid ethyl ester ethyi alcoholate Manufacturing Process... [Pg.597]

Acrylate and methacrylate polymerizations are accompanied by the Hberation of a considerable amount of heat and a substantial decrease in volume. Both of these factors strongly influence most manufacturing processes. Excess heat must be dissipated to avoid uncontrolled exothermic polymerizations. In general, the percentage of shrinkage decreases as the size of the alcohol substituent increases on a molar basis, the shrinkage is relatively constant (77). [Pg.165]

Survey and natural alcohols manufacture, Synthetic processes,... [Pg.439]

Most higher alcohols of commercial importance are primary alcohols secondary alcohols have more limited specialty uses. Detergent range alcohols are apt to be straight chain materials and are made either from natural fats and oils or by petrochemical processes. The plasticizer range alcohols are more likely to be branched chain materials and are made primarily by petrochemical processes. Whereas alcohols made from natural fats and oils are always linear, some petrochemical processes produce linear alcohols and others do not. Industrial manufacturing processes are discussed in Synthetic processes. [Pg.440]

Fig. 5. Flow diagram for oxo alcohol manufactured by the two-stage process. Courtesy of the Ethyl Corporation. Fig. 5. Flow diagram for oxo alcohol manufactured by the two-stage process. Courtesy of the Ethyl Corporation.
Magnesium methylate is used as a drying agent for alcohols and other organic solvents and as an intermediate in various manufacturing processes, eg, for organomagnesium compounds (79), orthocarbonic esters (80), and for oxide coatings. [Pg.27]

In this process, the fine powder of lithium phosphate used as catalyst is dispersed, and propylene oxide is fed at 300°C to the reactor, and the product, ahyl alcohol, together with unreacted propylene oxide is removed by distihation (25). By-products such as acetone and propionaldehyde, which are isomers of propylene oxide, are formed, but the conversion of propylene oxide is 40% and the selectivity to ahyl alcohol reaches more than 90% (25). However, ahyl alcohol obtained by this process contains approximately 0.6% of propanol. Until 1984, ah ahyl alcohol manufacturers were using this process. Since 1985 Showa Denko K.K. has produced ahyl alcohol industriahy by a new process which they developed (6,7). This process, which was developed partiy for the purpose of producing epichlorohydrin via ahyl alcohol as the intermediate, has the potential to be the main process for production of ahyl alcohol. The reaction scheme is as fohows ... [Pg.74]

Solubility. SolubiUty in water is less than 2% the solubiUty in ethanol is given by the ratio one part vanillin to two parts alcohol. Certain manufacturing processes require that the product be in Hquid form. Depending on the appHcation, the solvent must be chosen in accordance with the manufacturing process and regulation requirements. [Pg.397]

Poly(vinyl alcohol) can be derived from the hydrolysis of a variety of poly(vinyl esters), such as poly(vinyl acetate), poly(vinyl formate), and poly(vinyl ben2oate), and of poly(vinyl ethers). However, all commercially produced poly(vinyl alcohol) is manufactured by the hydrolysis of poly(vinyl acetate). The manufacturing process can be viewed as one segment that deals with the polymeri2ation of vinyl acetate and another that handles the hydrolysis of poly(vinyl acetate) to poly(vinyl alcohol). [Pg.482]

Irish Whiskey. Irish whiskeys are blends of grain and malt spirits three or more years of age that are produced in either the RepubHc of Ireland or Northern Ireland and comply with the respective laws regulating their manufacture. Since no peat is used in the malting process, Irish whiskey lacks the smokey character of Scotch. In the manufacturing process, the malt is soaked in water and milled to produce the wort. The fermentation usually takes about 60 hours. The first distillation in a pot stiU yields a 22—23% alcohol product. A second pot stiU distiUation produces a product that is 45—46% alcohol. This is foUowed by a third distiUation in another pot stiU to yield the Irish whiskey of about 68—70% alcohol. [Pg.82]

Isopropyl alcohol manufacture (strong acid process)... [Pg.91]

The most widely known aleohol is ethyl aleohol, simply beeause it is the aleohol in aleoholie drinks. It is also known as grain aleohol, or by its proper name, ethanol. Ethyl aleohol is a eolorless, volatile liquid with a eharaeteristie odor and a pungent taste. It has a flash point of 55°F, is classified as a depressant drug, and is toxic when ingested in large quantities. Its molecular formula is CjHjOH. In addition to its presence in alcoholic beverages, ethyl alcohol has many industrial and medical uses, such as a solvent in many manufacturing processes, as antifreeze, antiseptics, and cosmetics. [Pg.198]

The alternative manufacturing processes of higher molecular weight primary alcohols are given in Fig. 6. [Pg.25]

Alcohols obtained from fats and oils contain an even number of carbon atoms and they are completely linear. Alcohols obtained from petrochemical sources can be linear or branched, depending on the manufacturing process, and can also have even or odd numbers of carbon atoms. In many practical applications the small differences observed in the behavior of sulfated alcohols or indeed sulfated alcohol ethoxylates from either source is of no significance and the choice is made on economic grounds. [Pg.225]

Primary alcohols are produced either by the catalytic hydrogenation of methyl esters or by fatty acids derived from oils and fats, e.g., coconut oil (C12-C14) or tallow (Cl6-C18), or from synthetic sources. Alcohols manufactured from natural oils and fats and from the Ziegler-type processes produce even-numbered chain length primary alcohols. [Pg.672]

Iodometric analysis has been applied to the determination of griseofulvin in stages of the manufacturing process (37). The mycelium is extracted with chloroform and the analysis carried out in alcoholic solution. The 0.01N iodine solution is standardized with griseofulvic acid. [Pg.240]

Aldol addition, 2 63-64 acetone, 1 164 Aldolases, 3 675 4 711 Aldol process, for higher alcohol manufacture, 2 27t, 41-43 Aldonic acid, 14 132 Aldoses, 4 696... [Pg.27]

High-energy irradiation, silicone network preparation via, 22 567 High energy ruminant feeds, 10 864-865 High enriched uranium (HEU), 17 526 Higher aliphatic alcohols aldol process, 2 41-43 analysis, 2 9-10, lOt chemical reactions, 2 4-6 economic aspects, 2 7-9 health and safety factor, 2 6 manufacture from fats and oils, 2 12-19 oxo process (odd-numbered alcohols), 2 1, 10, 36-41... [Pg.434]


See other pages where Alcohol manufacturing process is mentioned: [Pg.40]    [Pg.479]    [Pg.40]    [Pg.479]    [Pg.239]    [Pg.443]    [Pg.444]    [Pg.445]    [Pg.446]    [Pg.208]    [Pg.208]    [Pg.74]    [Pg.208]    [Pg.286]    [Pg.257]    [Pg.531]    [Pg.449]    [Pg.133]    [Pg.435]    [Pg.225]    [Pg.897]    [Pg.292]    [Pg.292]    [Pg.187]    [Pg.210]    [Pg.908]   
See also in sourсe #XX -- [ Pg.115 ]




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