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principles of extraction and the extraction of semivolatile organics ...

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86 <strong>principles</strong> <strong>of</strong> <strong>extraction</strong><br />

S i l i c a<br />

sorbents available at <strong>the</strong> time. Reversed-phase bonded silica sorbents having<br />

alkyl groups covalently bonded to <strong>the</strong> silica gel backbone interact primarily<br />

with analytes via van der Waals forces (Figure 2.24).<br />

Bonded-phase sorbents are stable to aqueous solvents over a pH range <strong>of</strong><br />

1 to 8.5, above which <strong>the</strong> silica backbone itself begins to dissolve <strong>and</strong> below<br />

which <strong>the</strong> SiaC bond is attacked. Manufacturers have continued to extend<br />

<strong>the</strong>se ranges through improved products, <strong>and</strong> researchers have stretched<br />

<strong>the</strong> limits <strong>of</strong> <strong>the</strong>se restrictions. The development <strong>of</strong> bonded silica sorbents<br />

led to a proliferation <strong>of</strong> pharmaceutical <strong>and</strong> environmental applications for<br />

extracting <strong>semivolatile</strong> <strong>organics</strong> from aqueous solution.<br />

The bonded phases produced by manufacturers vary according to <strong>the</strong><br />

nature <strong>of</strong> <strong>the</strong> silica used to prepare <strong>the</strong> bonded phase <strong>and</strong> in <strong>the</strong> reactants<br />

<strong>and</strong> reaction conditions used. The variations are closely guarded, proprietary<br />

manufacturing processes. However, it is generally known that <strong>the</strong> most<br />

common commercially manufactured bonded-phase sorbents are based on<br />

chemical reaction between silica <strong>and</strong> organosilanes via <strong>the</strong> silanol groups on<br />

<strong>the</strong> silica surface to produce chemically stable SiaOaSiaC covalent linkages<br />

to <strong>the</strong> silica backbone [75,87]. Nonpolar, polar, or ionic bonded phases can<br />

be prepared by varying <strong>the</strong> nature <strong>of</strong> <strong>the</strong> organic moiety bonded to <strong>the</strong> silica<br />

surface.<br />

Bonded phases can be obtained as monomeric or polymeric coverage <strong>of</strong><br />

an organic lig<strong>and</strong> group, R, on <strong>the</strong> silica surface depending on whe<strong>the</strong>r a<br />

mon<strong>of</strong>unctional (R3SiX) or a trifunctional (RSiX3) reactant is used, respec-<br />

NH 2<br />

reversed-phase octadecyl (C 18 ) modified silica sorbent<br />

Figure 2.24. Interactions between analytes <strong>and</strong> nonpolar bonded silica sorbents via van der<br />

Waals forces.

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