Page 422 - Copper and Bronze in Art: Corrosion, Colorants, Getty Museum Conservation, By David Scott
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RECIPE  4  BLUE VERDITER
            There  are  practical  difficulties  in  manufacturing  blue  verditer.  Mactaggart  and  Mactaggart
            (i98o)  found that  15  g of cupric nitrate in 50 ml of water  mixed with  5 g of chalk produced
            pale  green  rodlike biréfringent  crystals, unsuitable  for  use  as  a pigment. With  15 g of cupric
            nitrate in 800 ml of water  and  5 g of chalk, kept between  6 °C and 20 °C for 24 hours, a green
            product was formed. This was synthetic malachite consisting of spherical particles with diame­
            ters between  2 and  15 μπι. These particles were highly biréfringent  with  a dark cross between
            crossed  polars.
               Finally, a blue verditer was produced on the third attempt using 200  ml of water and  15 g of
            cupric nitrate kept at below  12 °C and stirred at i-minute intervals. It took 5-9 hours  for blue
            crystals to form. Repeating the process using the first product formed as starting material caused
            the blue verditer particles to become  better formed, and diameters  up to 25  μιη  were produced.
           The low temperatures  are probably needed to enable enough carbon dioxide to stay in solution
            to  form a carbonic acid solution strong enough to influence the formation of the product within
            the azurite stability  field rather than in the malachite  field of stability predicted by the relevant
           Pourbaix  diagrams.


           RECIPE  5  SYNTHETIC CONNELLITE
           Pollard, Thomas,  and Williams  (1990  a)  prepared  connellite using  100  ml of water  and, while
           stirring, adding 0.725 g of cupric chloride dihydrate, 1.6055 g of sodium chloride, and  0.7 g of
           sodium sulfate decahydrate. Carbon dioxide - free 0.05  mol  sodium hydroxide solution was added
           until  the pH rose to  7.2.  The  fast  addition of hydroxide yields a blue phase of claringbullite,
                                                                               i
           Cu 8 (OH) 1 4 Cl 2 -H 2 0. This precipitate will recrystallize to connellite within  48 hours f the mix­
           ture is kept in a sealed container to exclude  C 0 2 ,  and it is regulated with a thermostat to 25 °C.


           RECIPE  6  SYNTHETIC  POSNJAKITE AND MALACHITE
           The  syntheses employed by Naumova, Pisavera,  and Nechiporenko  (1990)  are  described  here,
           although not all of the reaction conditions were specified by the authors. Posnjakite  was made
           by  adding powdered sodium bicarbonate  to copper  sulfate solution at an initial pH of 6.4-6.6.
           Precipitation of posnjakite occurred in  the broad range of pH  from  5.7 to 9. The precipitate crys­
           tallized on the  second  day. From a solution with  an initial pH 6.7, posnjakite  was mosdy pre­
           cipitated  as crystal twins and triplets and in the form of concretions. Posnjakite  obtained  from
           a near-neutral  solution appeared as lamellar crystals of rhombic or pseudohexagonal  form.
               For  the coprecipitation of posnjakite  and malachite, a sulfate solution was prepared  from
           copper  sulfate  containing 50 mg/1 of copper. A sodium bicarbonate  solution was poured into
           the  sulfate  solution and mixed with  a magnetic  stirrer. The  sodium bicarbonate  was  used  to






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