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104 The Role of the Chemist in Automotive Design<br />

7.10 syntHetIc esters<br />

Synthetic esters like polyol esters or neopentyl polyol esters are made from monobasic<br />

fatty acids and polyhedric alcohols with a neopentyl structure (see Figure 7.6).<br />

On these molecules, there are no hydrogen atoms on the beta carbon. This carbon<br />

is where thermal attack occurs on diesters and eliminating it improves the thermal<br />

stability of the molecule. Polyol esters have an increased number of ester groups<br />

versus diesters. This feature increases polarity, which will affect the lubricity of<br />

the oil at elevated temperatures and give it an advantage over PAOs.<br />

7.11 PolyoleFIns<br />

Polyolefins—specifically, polyalpha olefins—are made from polymerizing alpha<br />

olefins where the double bond is located at the alpha carbon atom. Figure 7.7 shows<br />

1-hexene. The double bond is located between the first and second carbon atoms<br />

and, as a result, they have flexible alkyl branching groups on every opposite carbon<br />

in the chain. The flexibility due to the different configurations makes crystallization<br />

difficult. Because polyalpha olefins are able to remain flexible at lower temperatures,<br />

they are ideal as a synthetic motor oil. Some advantages versus disadvantages of<br />

synthetics are shown in Table 7.4<br />

7.12 automatIc transmIssIon FluId (atF)<br />

The severity of the life of automatic transmission fluid is less severe than that<br />

of engine oil. Without the microscopic coke particles, soot, fuel interaction,<br />

and other contamination associated with motor oil, ATF must contend only<br />

with particles from friction plates and bearings from inside the transmission.<br />

Transmissions typically contain a nylon screen or filter of around 150 µ to filter<br />

out these particles; however, changing the fluid is the only way to eliminate them.<br />

The metallic particles present can contribute to the oxidation of the fluid and<br />

hasten its demise.<br />

H<br />

H<br />

C<br />

H 3 C<br />

H 3 C<br />

FIgure 7.6 Neopentyl glycol ester.<br />

FIgure 7.7 Structure of 1-hexene.<br />

C<br />

CH 2<br />

H<br />

CH 2<br />

O R<br />

n<br />

CH 2<br />

O<br />

Neopentyl glycol ester<br />

CH 2<br />

CH 3

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