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Introduction to Soil Chemistry

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128 extraction<br />

Organic compounds, including pollutants, can be desorbed from soil by<br />

heating using a procedure called headspace analysis. Heat-desorbed compounds<br />

can then be determined by gas chroma<strong>to</strong>graphy. A soil sample that<br />

does not fill the container is sealed inside the container using a cap containing<br />

a septum. The container is brought <strong>to</strong> a predetermined temperature and<br />

allowed <strong>to</strong> equilibrate. A syringe is inserted in<strong>to</strong> the sample container, and a<br />

sample of the headspace gas is removed and injected in<strong>to</strong> a gas chroma<strong>to</strong>graph<br />

(GC) or a gas chroma<strong>to</strong>graph–mass spectrometer (GC/MS) for separation and<br />

identification of the components released from the soil.<br />

There are other ways of removing components of interest from the soil<br />

matrix without using a solvent per se. Sparging, solid phase and solid-phase<br />

microextraction (SPME) are three of the most common of the nonsolvent<br />

methods.<br />

In sparging, a soil sample is placed in a container and a flow of gas, usually<br />

pure helium or nitrogen, is passed through it <strong>to</strong> remove components of interest.<br />

The soil may also be heated <strong>to</strong> remove components with lower vapor pressures.<br />

Gas exiting the container flows over a sorbant that removes or traps the<br />

components of interest. After a preset period of time at a prescribed temperature<br />

and flow rate, the flow is s<strong>to</strong>pped and sorbed components are extracted<br />

from the sorbant and analyzed by GC or GC/MS.<br />

Alternatively, the sorbant used in sparging can be placed directly in soil <strong>to</strong><br />

sorb components of interest. After a prescribed period of time, the sorbant is<br />

removed from soil, extracted, and analyzed by GC or GC/MS. In direct sorption<br />

there is always the question of contact between the sorbant and soil components.<br />

Therefore these procedures must be investigated <strong>to</strong> ascertain and<br />

validate their precision and accuracy.<br />

Direct heating of soil in a gas chroma<strong>to</strong>graph inlet and gas chroma<strong>to</strong>graphic<br />

analysis of released compounds from soil has also been used <strong>to</strong> analyze for<br />

absorbed compounds [1–9].<br />

7.2. EXTRACTION<br />

As a first step in any soil extraction, a decision between an aqueous and nonaqueous<br />

extracting solvent or solution is made.Typically inorganic compounds<br />

are extracted using either one of two types of aqueous solutions or in the simplest<br />

cases water. One type of aqueous solution containing a cation is designed<br />

<strong>to</strong> extract cations attached <strong>to</strong> exchange sites in the soil. Another is an aqueous<br />

solution containing ligands designed <strong>to</strong> form a strong attachment <strong>to</strong> the compound<br />

of interest. For simple, highly soluble compounds, a simple water extraction<br />

may be sufficient [10].<br />

In extracting cations and, in some cases, anions, the extracting solution must<br />

contain ions appropriate for accomplishing two tasks; they must (1) be capable<br />

of exchanging with the ion of interest and (2) not interfere with subsequent<br />

analytical procedures or analysis. Most commonly in soil the clay and organic<br />

matter carry a net negative charge and thus attract cations, resulting in soils

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