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Traditional Role of the Chemist in the Automobile Plant Environment 21<br />

The chemist in the automobile industry may be called upon not only for the manufacture<br />

of these compounds but also for the analysis in order to maintain the proper<br />

concentration of the compound. The detection in an HPLC system is most widely<br />

accomplished by UV-visible detectors. Most compounds used in production chemicals<br />

have chromophores that are detectable in the UV region. Table 2.6 shows molar<br />

absorption values for common functional groups [5]. Care must be taken that the solvent<br />

used in the analysis is invisible to the analysis. As can be seen from Table 2.6,<br />

typical detection range is 180–210 nm. A chromophore is the region between two<br />

different molecular orbitals and will absorb UV light due to the conjugated system<br />

of electrons or to a metal complex bound to a transition metal to a ligand.<br />

2.9 some Problems wItH HPlc as a lab tool<br />

In HPLC, an analyte is forced through a column of a stationary phase utilizing high<br />

pressure. A sample of the chemical being analyzed is then introduced into the mobile<br />

phase. Within the stationary phase, the sample will interact with the column material<br />

and be separated within the column by chemical and physical interactions. The<br />

variables of the sample itself, the column, and the mobile phase all contribute to<br />

the retention time on the column. As the separation of the sample occurs within the<br />

column, the pressure of the HPLC will increase the speed and reduce the diffusion<br />

seen in a normal chromatogram. Typically, methanol and acetonitrile are used as the<br />

solvent in the mobile phase for separations dealing with cutting fluids and hydraulic<br />

additives. Most often a gradient will be applied to vary the concentration of methanol/acetonitrile<br />

to enhance the separation.<br />

Reverse phase HPLC is also used due to the nature of the polar constituents that<br />

are examined. In reverse phase, the stationary phase is nonpolar and the mobile<br />

phase will be a mixture of polar solvents and aqueous media.<br />

Silica columns are generally used with long chain alkyl groups connected to<br />

R(CH 3) 2SiCl. The polar fats, amines, and other polar functional groups in the additive<br />

packages of concern will then come through the column more readily than the<br />

longer chain nonpolar components in the base oils. From the discussion on lubricity<br />

additives, one can see that reverse phase chromatography is a good choice for separation<br />

of these compounds.<br />

2.10 Plate tHeory and rate tHeory<br />

Martin and Synge first described plate theory in chromatography in the early 1940s<br />

[6]. Their thought was that a column can be considered as a long continuum of narrow<br />

horizontal layers called theoretical plates. These theoretical plates are discrete<br />

but thought of as being contiguous. Between the plates, equilibrium with the solute<br />

and the two phases takes place. Thinking of a separation this way envisions a stepwise<br />

process between each theoretical plate. A useful term, “height equivalent to<br />

theoretical plate, H,” is related to the efficiency of a column by the equation:

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