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            The trap comprised a quartz tube, 23 cm long, 3.7 mm O.D., 1.9 mm I.D. which was fitted with two
            heaters. The first heater maintained the temperature at 850-900°C  Mercury free oxygen was fed into
            the gas stream from the capillary column of the gas chromatograph, and the solutes were burnt in this
            first heated section. A valving system between the capillary column and the interface permitted selected
            peaks to be diverted to the trap as required. Subsequent to the combustion furnace was a section of tube
            containing gold-platinum wire (85% gold-15% platinum) that trapped all the mercury compounds by
            amalgamation. The section of the tube was also surrounded by a heater. When trapping was complete
            the mercury was desorbed from the gold-platinum wire by heating, and the mercury vapor was swept
            into the MIP atomic emission spectrometer. The results from this interface together with those obtained
            by the solid phase extraction procedure previously described are shown in Figure 6.11.



























                                                         Figure 6.11
                                 Measurement of Traces of Mercury in Natural Gas Condensate by Super
                                    Critical Fluid Extraction and by Selective Amalgamation (ref. 10)

            It is clear that the amalgam interface produces the highest sensitivity and it is seen that he back ground
            noise is extremely low. The trace from the
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