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Introduction to Soil Chemistry

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176 chroma<strong>to</strong>graphy<br />

Mobile<br />

phase<br />

Mobile<br />

phase<br />

aby<br />

aby<br />

a y<br />

a y<br />

a a<br />

b b<br />

b<br />

b<br />

This partitioning–separation process is diagramed in Figures 9.1 and 9.2. In<br />

Figure 9.1 a mixture is introduced in<strong>to</strong> a chroma<strong>to</strong>graphic column. The components<br />

are adsorbed on the stationary phase, and the component more<br />

soluble in the mobile phase moves in<strong>to</strong> this phase and is swept along the<br />

column, where it is adsorbed again. The less soluble component then moves<br />

in<strong>to</strong> the mobile phase and is again readsorbed by the stationary phase. In<br />

Figure 9.2 a mixture is introduced in<strong>to</strong> a chroma<strong>to</strong>graphic column, and as<br />

its components move down the column, they are separated in<strong>to</strong> discrete<br />

“packets” of the same compound and on exiting the column, they are detected.<br />

Table 9.1 summarizes the common chroma<strong>to</strong>graphic methods and the characteristics<br />

that differentiate them from other methods. In this list HPLC and<br />

GC are most commonly used in analyzing soil extracts, particularly when they<br />

are used in combination with mass spectral methods.<br />

9.2. GAS CHROMATOGRAPHY<br />

Stationary<br />

phase<br />

Figure 9.1. Partitioning of the components of a mixture in a chroma<strong>to</strong>graphic column.<br />

Gas chroma<strong>to</strong>graphy is a powerful, rapid method for separation of mixtures<br />

of gases and compounds with boiling points below ~400°C. 2 The sample, when<br />

2<br />

The temperature value 400°C is not an absolute upper limit of GC but is near the upper limit<br />

of most GC columns.

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