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Heavy Metals¡ªPipet 20 mL of the Sample Preparation Extract, filtered if necessary, intoone of two matched 50-mL color-comparison tubes. Adjust with 1 N acetic acid or 6 N ammonium hydroxide to a pH between 3.0 and 4.0, using short-range pH paper as an external indicator, dilute with water to about 35 mL, and mix. Into the second color-comparison tube pipet 2 mL of Standard Lead Solution (see Heavy Metals 231 ), and add 20 mL of the Blank. Adjust with 1 N acetic acid or 6 N ammonium hydroxide to a pH between 3.0 and 4.0, using short-range pH paper as an external indicator, dilute with water to about 35 mL, and mix. To each tube add 1.2 mL ofthioacetamide¨Cglycerin base TS and 2 mL of pH 3.5 Acetate Buffer (see Heavy Metals 231 ), dilute with water to 50 mL, and mix: any brown color produced within 10 minutes in the tube containing the Sample Preparation Extract does not exceed that in the tube containing the Standard Lead Solution, both tubes being viewed downward over a white surface (1 ppm in extract). |
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