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of  the solution on small wooden  sticks. This neutral monohydrate  is the best-known  salt, but
          even  here there  are  possibilities for  some variation in properties.  Laboratory research  at  the
          Getty Conservation  Institute showed  that  samples could be  prepared  that were  either  mono­
          clinic or triclinic in crystal habit.  APPENDIX D, TABLE  10,  shows  the results  of  a typical  exper­
                                    4
         iment to make a basic verdigris by the reaction of vinegar with copper  foil;  it only succeeded in
         producing another  example of the neutral salt corresponding  to ICDD  27-145. In 1998  Roy pro­
         vided the GCI Museum Research Laboratory with specimens of five different verdigris salts from
          the collections of the National Gallery of Art,  London.  Two of these corresponded  to the same
                                                     5
          salt produced in the previous experiment. Results of the Debye-Scherrer  powder X-ray diffrac­
          tion study of these samples are shown in APPENDIX  D, TABLE  11.
                                I  NEW VERDIGRIS  SYNTHESES  The previously published X-ray
         diffraction  data for the  basic copper (II)  acetates are  sometimes  contradictory and  difficult  to
         understand.  To rectify  this situation, a number  of new  syntheses were  carried out  at  the GCI
         Museum Research Laboratory using recipes designed  there,  as well  as  recipes from  Gauthier
          (i958); Schweizer and Mühlethaler (i968); and Rahn-Koltermann and colleagues  (1991). Histori­
          cal  pigment recipes were also replicated.
                         [
             Compound  A, C U ( C H 3 C O O ) 2 ] 2 - C U ( O H ) 2 - 5 H 2 0 ,  was  synthesized  using  a  recipe  from
          Gauthier  (quoted in Schweizer  and Mühlethaler  1968)  and by Rahn-Koltermann  and cowork­
          ers. Two syntheses for compound  A  are  described  in APPENDIX  B, RECIPE  8. Schweizer  and
         Mühlethaler's  synthesis of compound  Β is given in APPENDIX  B, RECIPE  9. Two syntheses of
          compound  c  are  given in  APPENDIX  B,  RECIPE  10. Data  for  additional  syntheses of com­
         pounds A,  B, and c  are given in APPENDIX  D, TABLE  12. The synthesis of compound  D,  as well
         as original recipes with samples provided by Roy,  is described in APPENDIX  B,  RECIPE  11.
             Rahn-Koltermann's  group  could not  synthesize  compound  B. The  author  was  successful,
         however, in producing five different solid products  that were removed at different stages of the
         reaction. APPENDIX D, TABLE  13, presents the following seven data sets: the author's five prod­
         ucts (labeled BI through Β 5) from  the synthesis of compound B; new data for the Schweizer  and
         Mühlethaler version of compound B; and data for a laboratory synthesis of compound A. Judg­
         ing  by the X-ray diffraction  data, most of these syntheses of Cu(CH 3 COO) 2 -Cu(OH) 2 -5H 2 0
         produced quite similar results.
                                                        COO)  [Cu  (OH)  2  O, was con­
                                                                      ]  3
             The National Gallery's sample of compound D, CU (CH 3  2  2  · H 2
         firmed  as  being  the  same  salt  as  the  one  derived  from  Schweizer  and  Mühlethaler's  recipe.
         APPENDIX  D, TABLE  14,  compares data for this sample with data for two syntheses (labeled  ytD
         and Ayt2)  from  the  GCI Museum Research Laboratory. APPENDIX  D,  TABLE  15, shows the value
         of  this newly revised and expanded  set of data: it was used to show that a light green verdigris
         pigment sample from  a manuscript had an X-ray diffraction  pattern that was an excellent match
         to  the author's  synthesis of compound  Β (sample  B4). The verdigris pigment is from Barlaam und





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