Propyl alcohol manufacture

Worldwide propylene production and capacity utilization for 1992 are given in Table 6 (74). The world capacity to produce propylene reached 41.5 X 10 t in 1992 the demand for propylene amounted to 32.3 x 10 t. About 80% of propylene produced worldwide was derived from steam crackers the balance came from refinery operations and propylene dehydrogenation. The manufacture of polypropylene, a thermoplastic resin, accounted for about 45% of the total demand. Demand for other uses included manufacture of acrylonitrile (qv), oxochemicals, propylene oxide (qv), cumene (qv), isopropyl alcohol (see Propyl alcohols), and polygas chemicals. Each of these markets accounted for about 5—15% of the propylene demand in 1992 (Table 7). 

The substitution of one hydroxyl radical for a hydrogen atom in propane produces propyl alcohol, or propanol, which has several uses. Its molecular formula is C3H7OH. Propyl alcohol has a flash point of 77°F and, like all the alcohols, bums with a pale blue flame. More commonly known is the isomer of propyl alcohol, isopropyl alcohol. Since it is an isomer, it has the same molecular formula as propyl alcohol but a different structural formula. Isopropyl alcohol has a flash point of 53 F. Its ignition temperamre is 850°F, while propyl alcohol s ignition temperature is 700 F, another effect of the different stmcture. Isopropyl alcohol, or 2-propanol (its proper name) is used in the manufacture of many different chemicals, but is best known as rubbing alcohol. 

There are two possible structures (isomers) of three carbon atom alcohol. C is n-propyl alcohol (or 1-propanol), the other is isopropyl alcohol (or 2-propanol). The former, no.. ..mufaetured in large quantities is used in printing inks. The latter is manufactured in millions of tons to make propylene by a process similar to that used to convert ethylene to ethanol. The manutaclure of 2-propanol by this process initiated the petrochemical industry in the 1920s. 

Isopropyl alcohol org chem (CH3)2CH0H A colorless liquid that boils at 82.4°Q soluble in water, ether, and ethanol used in manufacturing of acetone and its derivatives, of glycerol, and as a solvent. Also known as isopropanol 2-propanol sec-propyl alcohol. T-s3 pro-p3l al-k3,h6l ... 

Solvent manufacturer Honeywell Burdick Jackson [39] defines solvents as miscible if the two components can be mixed together in all proportions without forming two separate phases. A solvent miscibility chart (Figure 2.12) is a useful aid for determining which solvent pairs are immiscible and would therefore be potential candidates for use in LLE. More solvent combinations are miscible than immiscible, and more solvents are immiscible with water than with any other solvent. Solvents miscible with water in all proportions include acetone, acetonitrile, dimethyl acetamide, N,N-dimethylformamide, dimethyl sulfoxide, 1,4-dioxane, ethyl alcohol, glyme, isopropyl alcohol, methanol, 2-methoxyethanol, /V-methyI pyitoI idone. n-propyl alcohol, pyridine, tetrahydrofuran, and trifluoroacetic acid [40]. 

There are two major processes for the production of acetone (2-propanone). The feedstock for these is either Ao-propyl alcohol [(CH3)2CHOH] or cumene [ Ao-propyl benzene, C6H5CH(CH3)2]. In the last few years there has been a steady trend away from Ao-propyl alcohol and toward cumene, but Ao-propyl alcohol should continue as a precursor since manufacture of acetone from only cumene would require a balancing of the market with the coproduct phenol from this process. 

Propene is used for the manufacture of a variety of chemicals (Fig. 2), including polypropylene, acrylic acid, Ao-propyl alcohol, cumene, propy-... 

Alcohols are hydrocarbons with one or more hydrogen atoms substituted by hydroxyl (-OH) groups. Compounds with one hydroxyl group are called alcohols, those with two are called glycols, and those with three hydroxyls are called glycerols. Alcohols are used extensively in industries as solvents for the manufacture of a variety of products. Generally, all alcohols cause irritation to the mucous membranes with mild narcotic effect. There are important classes of alcohols, namely, allyl alcohol, amyl alcohol, n-butyl alcohol, methyl alcohol, ethyl alcohol, and propyl alcohol. 

Uses Propyl alcohol has two isomers, namely, n-Propyl alcohol and isopropyl alcohol. These alcohols have extensive use in a variety of industries (e.g., manufacturing, pharmaceuticals, perfumes, cosmetics, skin lotions, hair topics, mouthwashes, liquid soaps). It also is used in lacquers, dental lotions, polishers, and surgical antiseptics. 

Propyl hydroxid—Ethyl carbinol—Primary propyl alcohol— CH3,CH2,CH,0H—60—is produced, along with ethylic alcohol,dur-ing fermentation, and obtained by fractional distillation of marc brandy, from cognac oil, huile de marc (not to be confounded with oil of wine), an oily matter, possessing the flavor of inferior brandy, which separates from marc brandy, distilled at high temperatures and from the residues of manufacture of alcohol from beet-root, grain, molasses, etc. It is a colorless liquid, has a hot alcoholic taste, and a fruity odor boils at 96°.7 (306°.l F.) and is miscible with -water. It has not been put to any use in the arts. Its intoxicating and poisonous actions are greater than those of ethyl alcohol. It exists in small quantity in cider. 

Normal butyl alcohol, propyl carbinol, n-butanol, 1-buianol, CH3CH2CH2CH2OH. B.p. 117 C. Manufactured by reduction of crotonaldehyde (2-buienal) with H2 and a metallic catalyst. Forms esters with acids and is oxidized first to butanal and then to butanoic acid. U.S. production 1978 300 000 tonnes. 

The amines are a group of compounds with the general formula R-NHj, and all the common amines are hazardous. As a class the amines pose more than one hazard, being flammable, toxic, and, in some cases, corrosive. The amines are an analogous series of compounds and follow the naming pattern of the alkyl halides and the alcohols that is, the simplest amine is methyl amine, with the molecular formula of CH NHj. Methyl amine is a colorless gas with an ammonia-like odor and an ignition temperature of 806°F. It is a tissue irritant and toxic, and it is used as an intermediate in the manufacture of many chemicals. Ethyl amine is next in the series, followed by propyl amine, isopropyl amine, butyl amine and its isomers, and so on. 

Direct Oxidation. Direct oxidation of petroleum hydrocarbons has been practiced on a small scale since 1926 methanol, formaldehyde, and acetaldehyde are produced. A much larger project (29) began operating in 1945. The main product of the latter operation is acetic acid, used for the manufacture of cellulose acetate rayon. The oxidation process consists of mixing air with a butane-propane mixture and passing the compressed mixture over a catalyst in a tubular reaction furnace. The product mixture includes acetaldehyde, formaldehyde, acetone, propyl and butyl alcohols, methyl ethyl ketone, and propylene oxide and glycols. The acetaldehyde is oxidized to acetic acid in a separate plant. Thus the products of this operation are the same as those (or their derivatives) produced by olefin hydration and other aliphatic syntheses. 

Various modifications of the reaction of an alcohol with ammonia provide the most common commercial routes to alkylamines. Some others routes that are used to make certain individual amines include aldehyde/amine additions, nitrile reduction, the Ritter reaction, amination of isobutylene, and hydrogenation of anilines. Capacities of many plants depend on the product mix of mono/di/tri products as well as the variety of amines (ethyl, propyl and butyl). One must know the product mix that the capacity is based upon and the actual scheduled output of produces) to determine what amounts can actually be manufactured. Capacities are often in excess of anticipated demand to satisfy seasonal demands for pesticide uses116. 

There is a large quantity of data available on the German process for the manufacture of glycol ethers. The monomethyl, ethyl, and ra-propyl ethers of ethylene glycol are manufactured by the continuous reaction of ethylene oxide with the anhydrous alcohol at about 200 C and at 25-45 atm pressure. One volume of ethylene oxide and 6 vol. of alcbhol are fed... 

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