Page 130 - Analytical method for food addtives
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80  Analytical methods for food additives


              Procedure
              Preparation of the sample test solutions
              •  General
                 Remove high concentrations of ascorbic acid of more than 100 mg/kg or
                 100 mg/L of sample (see fruit juices). If the concentration of sulphite in the
                 sample test solution is higher than 0.3 g/L, dilute the sample test solution prior
                 to the determination or take a smaller sample volume.

              Liquid samples
              •  White wine, brandy and beer
                 Analyse white wine and brandy directly. Beer should be filtered to remove
                 carbon dioxide. It may be necessary to decolourise beer. For the decolourisa-
                 tion, add not more than about 0.7 g of bentonite to 10 mL of filtered beer in a
                 50 mL glass beaker, stir the mixture for 2 min using a magnetic stirrer and then
                 filter the solution into another 50 mL glass beaker.
                   For the enzymatic determination take 100 µL to 200 µL of wine or 500 µL
                 of brandy or beer respectively.
              •  Red wines
                 Adjust 25 mL of red wine to pH 7.5 to 8.0 with the sodium hydroxide solution
                 in a beaker. Transfer the solution into a 50 mL volumetric flask and dilute to
                 the mark with water and mix. It is often necessary to decolourise red wine. This
                 can be done as described for fruit juices.
              •  Fruit juices
                 Centrifuge cloudy juices at approximately 2000 g. Add 5 mL of juice into a
                 beaker and adjust the pH to 5 to 6 with the sodium hydroxide solution. Remove
                 ascorbic acid by adding approximately 40 units of ascorbate oxidase in
                 solution to the juice and leave the sample for 10 min, or remove the ascorbic
                 units by stirring for 3 min with an ascorbate oxidase spatula. Then adjust the
                 pH to 7.5 to 8.0 with the sodium hydroxide solution. In the case of coloured
                 juices, add approximately 0.25 g of polyvinylpolypyrrolidone and stir the
                 mixture for 1 min. Transfer the mixture to a 10 mL volumetric flask and dilute
                 with water. Filter the solution and take 200 µL for enzymatic determination.

              Solid foodstuffs

              Homogenise the sample thoroughly and extract with water at 60 °C for 5 min.
              Shake occasionally. Cool the sample to ambient temperature before analysing.
              Vary the sample size depending on the amount of sulphite. In the case of e.g. potato
              flakes, take 5.0 g of homogenised material into a 50 mL volumetric flask. Add
              40 mL of water. Close the flask and extract in a water bath at 60 °C for 5 min. Shake
              occasionally. Cool the volumetric flask, either by letting it stand for at least 15 min,
              to ambient temperature, or in a water bath of 20 °C, and dilute to the mark with
              water (V  = 50 mL). If necessary centifruge the solution.
                     3
                The following sample quantities of some other foods are suggested:
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