Gasoline commercial

While ethanol from wood sugars has not been part of that program, the successful substitution of ethanol for gasoline commercially has raised the prospect of a large market outlet, and the rapidly increasing price of gasoline here suggests that the economics, if not favorable now, may become so in a foreseeable future. 

OTHER COMMENTS main usage is in anti-knock additives for gasoline commercial products are impure, dyed red, orange or blue, with added stabilizer (1,2-dichloroethane, toluene) symptoms of encephalopathy do not become manifest until a delayed period of time. 

Commercially, xylene is obtained by the catalytic reforming of naphthenes in the presence of hydrogen see toluene) or was formerly obtained from coal tar. The material so-produced is suitable for use as a solvent or gasoline ingredient, these uses accounting for a large part of xylene consumption. If xylene is required as a chemical, separation into the iso-... 

Although they are small in absolute value, these fluctuations must be taken into account in the various commercial transactions related to storage and distribution of gasoline. 

The French specification for sulfur in all types of gasolines —regular, premium, with or without lead— is 0.1% maximum, that is, 1000 ppm. This value is easily achieved because in the majority of commercial products, the content is less than 500 ppm. 

The role of detergent additives is to maintain clean injectors so as to insure good distribution of diesel fuel in the cylinder. The structure of these compounds is similar to that of detergents for gasoline engine admission systems. Commercialized compounds are from the succinimide family (see Figure 9.1). 

We shonld also utilize liquid hydrocarbons, which frequently accompany natural gas. These so-called natural gas liquids currently have little use besides their caloric heat value. They consist mainly of saturated straight hydrocarbons chains containing 3-6 carbon atoms, as well as some aromatics. As we found (Chapter 8), it is possible by superacidic catalytic treatment to upgrade these liquids to high-octane, commercially usable gasoline. Their use will not per se solve our long-... 

The majority of xylenes, which are mostly produced by catalytic reforming or petroleum fractions, ate used in motor gasoline (see Gasoline and other MOTORFUELs). The majority of the xylenes that are recovered for petrochemicals use are used to produce PX and OX. PX is the most important commercial isomer. Almost all of the PX is converted to terephthaUc acid and dimethylterephthalate, and then to poly(ethylene terephthalate) for ultimate use in fibers, films, and resins. 

With aldehydes, primary alcohols readily form acetals, RCH(OR )2. Acetone also forms acetals (often called ketals), (CH2)2C(OR)2, in an exothermic reaction, but the equiUbrium concentration is small at ambient temperature. However, the methyl acetal of acetone, 2,2-dimethoxypropane [77-76-9] was once made commercially by reaction with methanol at low temperature for use as a gasoline additive (5). Isopropenyl methyl ether [116-11-OJ, useful as a hydroxyl blocking agent in urethane and epoxy polymer chemistry (6), is obtained in good yield by thermal pyrolysis of 2,2-dimethoxypropane. With other primary, secondary, and tertiary alcohols, the equiUbrium is progressively less favorable to the formation of ketals, in that order. However, acetals of acetone with other primary and secondary alcohols, and of other ketones, can be made from 2,2-dimethoxypropane by transacetalation procedures (7,8). Because they hydroly2e extensively, ketals of primary and especially secondary alcohols are effective water scavengers. 

If 10% of the U.S. gasoline consumption were replaced by methanol for a twenty year period, the required reserves of natural gas to support that methanol consumption would amount to about one trillion m (36 TCF) or twice the 1990 annual consumption. Thus the United States could easily support a substantial methanol program from domestic reserves. However, the value of domestic natural gas is quite high. Almost all of the gas has access through the extensive pipeline distribution system to industrial, commercial, and domestic markets and the value of gas in these markets makes methanol produced from domestic natural gas uncompetitive with gasoline and diesel fuel, unless oil prices are very high. 

Separation of Aromatic and Aliphatic Hydrocarbons. Aromatics extraction for aromatics production, treatment of jet fuel kerosene, and enrichment of gasoline fractions is one of the most important appHcations of solvent extraction. The various commercial processes are summarized in Table 4. 

In the eady 1980s, the process was commercialized in New Zealand to convert offshore natural gas to 2200 m /day (14,000 barrels/day) gasoline. Since then some of the methanol has been diverted from fuel production to chemical-grade methanol production by a dding additional methanol refining capacity. 

TaF has been characterized by ir, Raman, x-ray diffraction, and mass spectrometry (3,11,12). TaF has been used as a superacid catalyst for the conversion of CH to gasoline-range hydrocarbons (qv) (12) in the manufacture of fluoride glass and fluoride glass optical fiber preforms (13), and incorporated in semiconductor devices (14). TaF is also a catalyst for the Hquid-phase addition of HF to polychlorinated ethenes (15). The chemistry of TaF has been reviewed (1,16—19). Total commercial production for TaF is thought to be no more than a few hundred kilograms aimuaHy. 

Natural Gas Upgrading via Fischer-Tropsch. In the United States, as in other countries, scarcities from World War II revived interest in the synthesis of fuel substances. A study of the economics of Fischer synthesis led to the conclusion that the large-scale production of gasoline from natural gas offered hope for commercial utiHty. In the Hydrocol process (Hydrocarbon Research, Inc.) natural gas was treated with high purity oxygen to produce the synthesis gas which was converted in fluidized beds of kon catalysts (42). 

Hexane refers to the straight-chain hydrocarbon, C H branched hydrocarbons of the same formula are isohexanes. Hexanes include the branched compounds, 2-methylpentane, 3-methylpentane, 2,2-dimethylbutane, 2,3-dimethylbutane, and the straight-chain compound, / -hexane. Commercial hexane is a narrow-boiling mixture of these compounds with methylcyclopentane, cyclohexane, and benzene (qv) minor amounts of and hydrocarbons also may be present. Hydrocarbons in commercial hexane are found chiefly in straight-mn gasoline which is produced from cmde oil and natural gas Hquids (see Gasoline AND OTHER MOTOR fuels Gas,natural). Smaller volumes occur in certain petroleum refinery streams. 

Mixtures of CO—H2 produced from hydrocarbons, as shown in the first two of these reactions, ate called synthesis gas. Synthesis gas is a commercial intermediate from which a wide variety of chemicals are produced. A principal, and frequendy the only source of hydrogen used in refineries is a by-product of the catalytic reforming process for making octane-contributing components for gasoline (see Gasoline and OTHER MOTOR fuels), eg. 

Linear a-olefins were produced by wax cracking from about 1962 to about 1985, and were first commercially produced from ethylene in 1965. More recent developments have been the recovery of pentene and hexene from gasoline fractions (1994) and a revival of an older technology, the production of higher carbon-number olefins from fatty alcohols. 

The naphtha fraction is dorninated by saturates having lesser amounts of mono- and diaromatics (Table 2, Eig. 4). Whereas naphtha (ibp to 210°C) covers the boiling range of gasoline, most raw petroleum naphtha molecules have a low octane number and most raw naphtha is processed further, to be combined with other process naphthas and additives to formulate commercial gasoline. 

The odd-carbon stmcture and the extent of branching provide amyl alcohols with unique physical and solubiUty properties and often offer ideal properties for solvent, surfactant, extraction, gasoline additive, and fragrance appHcations. Amyl alcohols have been produced by various commercial processes ia past years. Today the most important iadustrial process is low pressure rhodium-cataly2ed hydroformylation (oxo process) of butenes. 

The hydroperoxide process involves oxidation of propjiene (qv) to propylene oxide by an organic hydroperoxide. An alcohol is produced as a coproduct. Two different hydroperoxides are used commercially that result in / fZ-butanol or 1-phenylethanol as the coproduct. The / fZ-butanol (TBA) has been used as a gasoline additive, dehydrated to isobutjiene, and used as feedstock to produce methyl tert-huty ether (MTBE), a gasoline additive. The 1-phenyl ethanol is dehydrated to styrene. ARCO Chemical has plants producing the TBA coproduct in the United States, Erance, and the Netherlands. Texaco has a TBA coproduct plant in the United States. Styrene coproduct plants are operated by ARCO Chemical in the United States and Japan, Shell in the Netherlands, Repsol in Spain, and Yukong in South Korea. 

Stannic Chloride. Stannic chloride is available commercially as anhydrous stannic chloride, SnCl (tin(IV) chloride) stannic chloride pentahydrate, SnCl 5H20 and in proprietary solutions for special appHcations. Anhydrous stannic chloride, a colorless Aiming Hquid, fumes only in moist air, with the subsequent hydrolysis producing finely divided hydrated tin oxide or basic chloride. It is soluble in water, carbon tetrachloride, benzene, toluene, kerosene, gasoline, methanol, and many other organic solvents. With water, it forms a number of hydrates, of which the most important is the pentahydrate. Although stannic chloride is an almost perfect electrical insulator, traces of water make it a weak conductor. 

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