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Dibasic acid esters

Dibasic Acid Esters. Dibasic acid esters (diesters) are prepared by the reaction of a dibasic acid with an alcohol that contains one reactive hydroxyl group (see Esters, organic). The backbone of the stmcture is formed by the acid. The alcohol radicals are joined to the ends of the acid. The physical properties of the final product can be varied by using different alcohols or acids. Compounds that are typically used are adipic, azelaic, and sebacic acids and 2-ethyIhexyl, 3,5,5-trimethyIhexyl, isodecyl, and tridecyl alcohols. [Pg.264]

Dibasic acid esters and polyol esters are used as the bases in all aircraft jet-engine lubricants. They also are employed in aircraft greases that are subjected to wide temperature ranges. [Pg.272]

Synthetic oils have been classified by ASTM into synthetic hydrocarbons, organic esters, others, and blends. Synthetic oils may contain the following compounds diaLkylben2enes, poly(a-olefins) polyisobutylene, cycloaUphatics, dibasic acid esters, polyol esters, phosphate esters, siUcate esters, polyglycols, polyphenyl ethers, siUcones, chlorofluorocarbon polymers, and perfluoroalkyl polyethers. [Pg.368]

Miscellaneous Commercial Applications. Dimer acids are components of "downweU" corrosion inhibitors for oil-drilling equipment (see Petroleum Corrosion and corrosion inhibitors). This may account for 10% of current dimer acid use (71). The acids, alkyl esters, and polyoxyalkylene dimer esters are used commercially as components of metal-working lubricants (see Lubrication). Dimer esters have achieved some use in specialty lubricant appHcations such as gear oils and compressor lubricants. The dimer esters, compared to dibasic acid esters, polyol esters and poly(a-olefin)s, are higher in cost and of higher viscosity. The higher viscosity, however, is an advantage in some specialties, and the dimer esters are very stable thermally and can be made quite oxidatively stable by choice of proper additives. [Pg.117]

Plasticizers. Plasticizers are materials that soften and flexibilize inherently rigid, and even britde polymers. Organic esters are widely used as plasticizers in polymers (97,98). These esters include the benzoats, phthalates, terephthalates, and trimeUitates, and aUphatic dibasic acid esters. Eor example, triethylene glycol bis(2-ethylbutyrate) [95-08-9] is a plasticizer for poly(vinyl butyral) [63148-65-2] which is used in laminated safety glass (see Vinyl POLYMERS, poly(vinyl acetals)). Di(2-ethyUiexyl)phthalate [117-81-7] (DOP) is a preeminent plasticizer. Variation of acid and/or alcohol component(s) modifies the efficacy of the resultant ester as a plasticizer. In phthalate plasticizers, molecular sizes of the alcohol moiety can be varied from methyl to tridecyl to control permanence, compatibiUty, and efficiency branched (eg, 2-ethylhexyl, isodecyl) for rapid absorption and fusion linear (C6—Cll) for low temperature flexibiUty and low volatility and aromatic (benzyl) for solvating. Terephthalates are recognized for their migration resistance, and trimeUitates for their low volatility in plasticizer appHcations. [Pg.396]

In a fully synthetic oil, there is almost certainly some mineral oil present. The chemical components used to manufacture the additive package and the viscosity index improver (VI) contain mineral oil. When all these aspects are considered, it is possible for a "fully synthetic" engine oil to surpass mineral oil (Shubkin, 1993). Synthetic oils fall into general ASTM classification (a) synthetic hydrocarbons (poly-a-olefins, alkylated aromatics, cycloaliphatics) (b) organic esters (dibasic acid esters, polyol esters, polyesters) (c) other fluids (polyalkylene glycols, phosphate esters, silicates, silicones, polyphenyl esters, fluorocarbons). [Pg.49]

Reaction sequence 2.10 Thermal decomposition of (a) esters with -hydrogens (e.g. dibasic acid esters) and (b) esters without fl-hydrogens (e.g. neopolyol esters). [Pg.58]

From Dibasic Acids Esters and Dimercaptans (Reaction E/M). This transesterification (31) offers some advantages over other methods. [Pg.125]

Axarel 32/ Petroferm Semiaqueous defluxer mixed aliphatic hydrocarbons, diisobutyl dibasic acid ester mixture, and Alkyloxy polyethylene oxyethanol (KB value = 64) Removal of ionic contamination and residual rosin when used with water rinsing N/A 2.8 N/A 96 <0.1... [Pg.184]

Dibasic Acid Esters DBE 1119-40-0 212.0 Combustible Class IIIB or NOS 1.40% 14.30%... [Pg.298]

Dibasic Acid Esters DBE-6 627-93-0 235.4 Combustible Class IIIB or NOS 0.81 % 8.10%... [Pg.298]


See other pages where Dibasic acid esters is mentioned: [Pg.296]    [Pg.263]    [Pg.264]    [Pg.296]    [Pg.945]    [Pg.151]    [Pg.152]    [Pg.159]    [Pg.769]    [Pg.581]    [Pg.583]    [Pg.396]    [Pg.384]    [Pg.5063]    [Pg.237]    [Pg.237]    [Pg.237]    [Pg.258]    [Pg.258]    [Pg.259]    [Pg.269]    [Pg.269]    [Pg.269]    [Pg.279]    [Pg.279]    [Pg.279]    [Pg.289]    [Pg.289]    [Pg.308]    [Pg.308]    [Pg.308]    [Pg.318]    [Pg.318]    [Pg.318]   
See also in sourсe #XX -- [ Pg.151 ]




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