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Alcohol-esters fuels

The economics and processing to make these alcohol-ester fuels -as octane enhancers for unleaded gasoline - have been reviewed (7). [Pg.20]

Commercialization of the novel syngas-to-alcohol-ester fuels (7), syngas acetic acid (125), and SFA processes (96,97) described in this review will hinge primarily upon projected 1990 s economics, particularly the relative feedstock values of petroleum and natural products, versus synthesis gas derived from coal or natural gas. [Pg.51]

Polyacetals are resistant to aldehydes, ketones, alcohols, esters, fuels, lube oils, and hydraulic fluids. Both are attacked by oxidizing agents and strong acids, and both lose property levels when exposed to phenols and aniline at elevated temperatures over a long time (Table 5.6). [Pg.92]

This approach to the preliminary assessment of the potential of biomass energy presumes that suitable conversion processes are available for conversion of biomass to SNG. Other processes could be used to manufacture other synfuels such as synthesis gas, alcohols, esters, and hydrocarbons. The direct route, alluded to in Fig. 2.1 as natural production of hydrocarbons, can possibly bypass the harvesting-conversion routes. As already mentioned, some biomass species produce hydrocarbons as metabolic products. Natural rubber, glycerides, and terpenes from selected biomass species, for example, as well as other reduced compounds could be extracted and refined to yield conventional or substitute fossil fuels. [Pg.41]

Drown, D.C. K. Harper E. Frame. Screening vegetable oil alcohol esters as fuel lubricity enhancers. /. Am. Oil Chem. Soc. 2001, 78, 579-584. [Pg.535]

C1-C4 Alcohol/acetate ester fuel products - potential octane enhancers - using Ru in combination with cobalt, titanium or zirconium (7). [Pg.3]

Early in the development of atomic absorption spectroscopy it was recognized that enhanced absorbances could be obtained if the solutions contained low-molecular-weight alcohols, esters, or ketones. The effect of organic solvents is largely attributable to increased nebulizer efficiency the lower surface tension of sueh solutions results in smaller drop sizes and a resulting increase in the amount of sample that reaches the flame. In addition, more rapid solvent evaporation may also contribute to the effect. Leaner fuel-oxidant ratios must be used with organic solvents to offset the presence of the added organic material. Unfortunately, however, the leaner mixture produces lower flame temperatures and an increased potential for chemical interferences. [Pg.132]

PE-HD is resistant to hot water, mineral acids, bases, inorganic salt solutions, aliphatic hydrocarbons, alcohols, esters, ketones, mineral oils, amines, organic acids, fats, oils, and fuels. PE-HD is not resistant to oxidizing acids, aromatic hydrocarbons, and detergents (depending on the type). Creep tests with PE-HD show a strikingly large difference between creep times in water and air [810]. [Pg.716]

Butadiene rubber is not resistant to mineral oils and fuels. However, butadiene rubber is resistant to alcohols, esters, glycols, and non-oxidizing acids. Butadiene-rubber is not resistant to chlorinated hydrocarbons, including vegetable and animal fats and oils. Water absorption is low [697]. [Pg.810]

There are no universal adhesives for the diverse applications seen in the aerospace business. Adhesives not only have to operate in space applications from about - 100 to - - 120°C, in civil and military aircraft under hot/wet climatic conditions, where relative humidities can approach 100% at temperatures up to 60-80°C, and close to aero engine assemblies where temperatures can reach in excess of 220°C but also have to resist the numerous fluids which are present in most modern aircraft de-icing fluid (alcohols and phosphate esters), fuels, bilge fluid, oils and lubricants, water and water-based electrolytes. [Pg.261]

Lubricants, Fuels, and Petroleum. The adipate and azelate diesters of through alcohols, as weU as those of tridecyl alcohol, are used as synthetic lubricants, hydrauHc fluids, and brake fluids. Phosphate esters are utilized as industrial and aviation functional fluids and to a smaH extent as additives in other lubricants. A number of alcohols, particularly the Cg materials, are employed to produce zinc dialkyldithiophosphates as lubricant antiwear additives. A smaH amount is used to make viscosity index improvers for lubricating oils. 2-Ethylhexyl nitrate [24247-96-7] serves as a cetane improver for diesel fuels and hexanol is used as an additive to fuel oil or other fuels (57). Various enhanced oil recovery processes utilize formulations containing hexanol or heptanol to displace oil from underground reservoirs (58) the alcohols and derivatives are also used as defoamers in oil production. [Pg.450]

The reactants are fed separately iato a stUl, from which the product is continuously removed by distillation (qv) (31). Isopropyl nitrate is a valuable engiae-starter fuel and can be used ia explosives (see Explosives and propellants) (32). The nitrite ester, isopropyl nitrite, can be prepared from the reaction of isopropyl alcohol and either nitrosyl chloride or nitrous acid at ambient temperature (33). The ester is used as a jet engine propellant (30). [Pg.106]

These mixed phosphate ester titanium complexes or their amine salts are useful as fuel additives to help maintain cleanliness of carburetors and inhibit surface corrosion. Chloride-free mixed alcohol phosphate esters can be obtained if a tetraalkyl titanate is used (101). [Pg.147]

Both the dipolymers and terpolymers have excellent resistance to hydrocarbons found m petroleum-based fuels and lubricants The 69 5% F terpolymer resists swellmg m blended fuels that contain metlianol and can be used in contact with certain phosphate ester-based hydraulic fluids Terpolymers are preferred for contact with aromatic solvents, although either type performs well in higher alcohols VDF-based elastomers dissolve m polar aprotic solvents such as ketones, esters, amides, and certam ethers These elastomers are therefore not suitable for contact with fluids that contain substantial amounts of these solvents because of excessive swell and consequent loss of mechanical properties... [Pg.1113]

With the discussion of oxygenafe, pofentially bioderived, fuels and fuel additives such as alcohols, ethers, or esters, the need for defailed information on their combustion chemistries is becoming acute. Additional functional groups in the fuel molecule lead to a larger number of possible structural isomers. The influence of the chemical structure of the fuel molecule... [Pg.10]

Alcohols form esters from inorganic acids as shown above. Like all esterifications, these reactions are reversible that is, in the presence of water and the right conditions, they revert to the original alcohol and acid. Nitrate esters are mainly used as explosives, but some have found use as diesel fuel additives. Note the difference between a nitrate ester such as ethyl nitrate (C2H5ONO2) and an organic nitro compound such as nitroethane (C2H5NO2). [Pg.68]


See other pages where Alcohol-esters fuels is mentioned: [Pg.1]    [Pg.13]    [Pg.1]    [Pg.13]    [Pg.59]    [Pg.226]    [Pg.255]    [Pg.320]    [Pg.48]    [Pg.60]    [Pg.1645]    [Pg.255]    [Pg.1631]    [Pg.400]    [Pg.130]    [Pg.601]    [Pg.155]    [Pg.320]    [Pg.356]    [Pg.359]    [Pg.133]    [Pg.447]    [Pg.399]    [Pg.194]    [Pg.347]    [Pg.512]    [Pg.158]    [Pg.216]    [Pg.236]    [Pg.428]    [Pg.801]    [Pg.313]    [Pg.1032]    [Pg.292]    [Pg.86]   
See also in sourсe #XX -- [ Pg.11 ]




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Alcohol fuels

Alcoholic esters

Esters alcohols

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