Page 433 - Copper and Bronze in Art: Corrosion, Colorants, Getty Museum Conservation, By David Scott
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RECIPE  25  COPPER  ORTHOARSENITE
         Copper  orthoarsenite  was  made in the laboratory following  Gmelin's  (i965)  recipe  as  follows:
         In a 31 beaker, 56.2 g of CuS0 4 -  5 H 2 0 was dissolved in 375 ml of water and heated to boiling. In
         an 800 ml beaker, 13.33 g of  A s 2 0 3  and  7.16 g of Na 2 CO s  (hydrate) were  dissolved in 585 ml of
         water. The  A s 2 0 3 and  Na 2 C0 3 solution was gendy heated to the boiling point until all the  A s 2 0 3
         had dissolved. The solution was then allowed to cook for 5 minutes to expel all of the free  C 0 2 .
         A  heated solution of copper  sulfate  was  added  to  the  first  solution drop by drop until  a pre­
         cipitate had formed. This fine green powder precipitate was cooked in suspension for  another
         5 minutes,  then  cooled,  filtered  off, and washed  well with  hot water.  Finally,  the product  was
         dried at loo °C.


         RECIPE  26  COPPER  DIARSENATE I
         Copper diarsenate I was made in the laboratory following Gmelin's (i965) recipe,  as follows: In
         a 3 1 beaker, îoo g of CuS0 4 -  5 H 2 0 was dissolved in 364 ml of cold water  (the solution is nearly
         saturated).  A solution of NaAs0 2 was prepared  with  12.73 g of  Na 2 C0 3  and  23.75 g of  A s 2 0 3 in
         312 ml of water,  expelling the  C 0 2  by gently bringing the  solution to  a boil  and  cooking for
         5 minutes. The  solution was  then  cooled to room temperature  and  precipitated  at 22-24 °C.
         The precipitated product was allowed to stand  overnight. Because the suspension is very  diffi­
         cult to filter, it is easier to make the precipitate into a paste. Water was added  to the paste twice,
         then decanted. This washing process does not take too long because the product hydrolyzes eas­
         ily. The product was dried at 100 °C.


         RECIPE  27  EMERALD  GREEN,  BEARN'S METHOD
         Emerald green was made in the laboratory, following Beam's (1923) recipe by dissolving 2.5 g of
         sodium carbonate in 100 ml of water  and  slowly stirring in 5 g of arsenious oxide, which dis­
         solves with  heating in about  30 minutes. Next, 6.25 g of cupric sulfate  was  dissolved in I80 ml
         of water  and heated to about  90 °C. Adding the sodium arsenite solution precipitated the  cop­
         per  arsenite,  which  was  redissolved in dilute acetic  acid  (15% v/v). The resulting solution was
         gently boiled and then cooled, at which point the bright green salt of the acetoarsenite (emerald
         green)  separated out. This was  filtered,  washed in hot water, and dried.


         RECIPE  28  EMERALD  GREEN, GMELIN'S  RECIPE 1
         Emerald green was synthesized using Gmelin's (i965) recipe 1 as follows: In a three-necked  flask
         of about 250 ml capacity and equipped with a thermometer  and stirrer, 7.8 g of neutral verdigris
         was  dissolved in 100 ml of water, and  the solution was heated to 70 °C. With  stirring,  7.8 g of
         arsenious oxide was  added,  which  took about  10 minutes. The solution was  heated to boiling






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