Page 296 - Vogel's TEXTBOOK OF QUANTITATIVE CHEMICAL ANALYSIS
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1-Naphtholphthalein.  Dissolve  1 g of  the indicator  in  500 mL of  ethanol and
       dilute with 500 mL of  water.

       Phenolphthalein.  Dissolve  5 g  of  the  reagent  in  500 mL  of  ethanol  and  add
       500 mL of water with constant stirring. Filter, if  a precipitate forms.
         Alternatively,  dissolve  1 g of  the dry indicator in  60 mL of 2-ethoxyethanol
       (Cellosolve), b.p. 135 OC,  and dilute to 100 mL with distilled water: the loss by
       evaporation is less with this preparation.
       Thymolphthalein.  Dissolve 0.4 g of the reagent in  600 mL of ethanol and add
       400 mL of water with stirring.
       Sulphonphthaleins.  These indicators are usually supplied in the acid form. They
       are rendered water-soluble by adding sufficient sodium hydroxide to neutralise
       the  sulphonic acid  group. One gram  of  the  indicator  is  triturated  in  a  clean
       glass mortar with the appropriate quantity of 0.1  M sodium hydroxide solution,
       and  then  diluted  with  water  to  1 L. The following  volumes  of  0.1 M  sodium
       hydroxide  are required  for  1 g of  the indicators: bromophenol  blue,  15.0 mL;
       bromocresol  green,  14.4 mL; bromocresol  purple,  18.6 mL; chlorophenol  red,
       23.6 mL;  bromothymol  blue,  16.0 mL;  phenol  red,  28.4 mL;  thymol  blue,
       21.5 mL; cresol red, 26.2 mL; metacresol purple, 26.2 mL.

       Quinaldine red.  Dissolve  1 g in  100 mL of  80 per cent ethanol.
       Methyl yellow, neutral red, and Congo red.  Dissolve  1 g of the indicator in  1 L
       of  80 per cent ethanol. Congo red may also be dissolved in water.
       4-Nitrophenol.  Dissolve 2 g of  the solid in 1 L of  water.
       Alizarin yellow R.  Dissolve 0.5 g of the indicator in  1 L of  80 per cent ethanol.
       Tropaeolin O and tropaeolin 00. Dissolve  1 g of  the solid in  1 L of  water.
         Many  of  the  indicator  solutions  are  available  from  commercial  suppliers
       already prepared  for use.




       For some purposes it is desirable to have a sharp colour change over a narrow
       and  selected  range of  pH; this  is  not  easily seen with  an ordinary  acid-base
       indicator, since the colour change extends over two units of  pH. The required
       result may, however, be achieved by the use of  a suitable mixture of indicators;
       these are generally selected so that their pK;,  values are close together and the
       overlapping  colours  are complementary at an intermediate pH  value.  A few
       examples  will be given in some detail.
       (a) A mixture of  equal parts  of  neutral red (0.1 per cent solution in ethanol)
          and methylene blue (0.1 per cent solution in ethanol) gives a sharp colour
          change from violet-blue  to green in passing from acid to alkaline solution
          at pH  7. This indicator may  be employed to titrate acetic acid (ethanoic
          acid)  with  ammonia  solution  or  vice  versa.  Both  acid  and  base  are
          approximately of the same strength, hence the equivalence point will be at
          a  pH N 7 (Section  10.15); owing to  the extensive  hydrolysis  and  the flat
          nature of the titration curve, the titration cannot be performed  except with
          an indicator of very narrow range.
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