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É«Æ×·ÖÎöÈéËá¼×õ¥ ÈéËá ¼×´¼ Ë® £¬ÈçºÎÈ·¶¨É«Æ×·ÖÎöÌõ¼þ£¬ÒºÏàÉ«Æ×ºÃ£¬»¹ÊÇÆøÏàÉ«Æ×ºÃ£¬ÈçºÎ´ÓÎÄÏ×Öп´³öÎÒÐèÒªµÄÉ«Æ×Ìõ¼þ£¬Ê¹ÓÃÉ«Æ×·ÖÎöʱ£¬·ÖÎöÌõ¼þ³ýÁ˽øÑùÎÂ¶È ¼ì²âÊÒÎÂ¶È Éýη½·¨ ÔØÆø£¬»¹ÓÐÊ²Ã´ÄØ£¬ Sample Analysis. The samples were analyzed using a Hewlett-Packard (6890) gas chromatograph (GC) equipped with series connected thermal conductivity and flame ionization detectors so that water and the other components could be detected in the same run. The GC column was a 25 m 0.25 mm bonded phase fused silica capillary column. Helium, 99.999% pure, was used as carrier gas. The injector and detectors were at 503.15 K and 533.15 K, respectively. The oven was operated at programmed temperature, from 353 K to 493 K at a rate of 40 K min-1. 1,2-Propanediol was used as internal standard for analysis of the quaternary samples. The estimated uncertainty in phase compositions was (0.0005 mole fraction. Quantitative analysis of monomeric lactic acid in the vapor phase was also carried out by titration with sodium hydroxide, using phenolphthalein as the indicator. This method is only accurate for very weak lactic acid solutions.12 |
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