Page 371 - Copper and Bronze in Art: Corrosion, Colorants, Getty Museum Conservation, By David Scott
P. 371

Norman (i988) recounts  that in the 1920s the Fitzwilliam Museum in Cambridge, England,
            was sending its bronzes to the Ashmolean Museum in Oxford for conservation. The Honorary
            Keeper of Antiquities at the Fitzwilliam was  so horrified, however, when the objects  came back
            with their surfaces a chocolate-brown cuprite or coppery metal that the museum devised its own
            conservation  methods.  Norman  infers  that  the  damaging  treatment  used in  Oxford  was  the
            zinc granule  and  sodium hydroxide method  that  had  been published  first  by Rathgen  (1905)
            and later by Scott  (1926). Rathgen  notes that the treatment, known as "Krefting's Method," had
            been in use in Denmark since  at least 1887 (Krefting  1892a,b). With this treatment,  the object is
            immersed in a 10% (w/v) solution of sodium hydroxide, usually warmed on a hot plate, to which
            zinc granules  are added. This reaction, given in equation  12.1, has long been used in the labora­
            tory to produce  hydrogen.

                                    Zn  +  2NaOH = Na 2 Zn0 2  +  H 2               12.1

            This  reaction  electrochemically reduced  the  corrosion products  on the  immersed  object,  and
            these products would  fall  away  as a precipitate in the sodium zincate  solution. Because of the
            electrochemical potential between  copper  and zinc, the end result might be a surface  leached of
            alloying elements over which zinc metal precipitated from  solution; or the partial elimination
            of  a cuprite patina  might produce  the  undesirable  subfusc  surfaces  that  elicited such  horror
            from  the Fitzwilliam Museum curator.
               The  treated  bronzes  at  the  Fitzwilliam  Museum  were  sometimes  polished  after  electro­
            chemical reduction, but they were never lacquered. Further deterioration may occur  as a result
            of these chemical-stripping techniques,  as in the example  cited by Norman, in which  a leaded
            bronze  treated  with  this technique  now has  a thin  gray-to-white deposit  over most of its sur­
            face. The corrosion of the lead component of this bronze  was probably exacerbated by the  use
            of the patina-stripping techniques, which would have exposed  the bare metallic surface  to more
            immediate deterioration as a result of organic acid pollutants within the display case.
               Jaeschke and Jaeschke (i988) reviewed the treatment  records of some Egyptian bronzes in
            the Petrie Museum of University College, London. During the  1950s and  1960s, many of these
            bronzes were treated using the sodium sesquicarbonate method, in which bronzes are immersed
            for long periods of time in a 10% solution of sodium sesquicarbonate in distilled water, and  the
            release of chloride ions is monitored during the treatment. During the re-treatment  of one  such
            object in 1982, small yellow metallic flakes occurred on the  surface,  which were probably par­
            ticles of redeposited  copper  produced  as  a consequence of the  earlier  conservation  treatment
            with sodium sesquicarbonate. The change in appearance of the copper particles may have been
            due  to the highly alkaline environment of the  treated  surface  of the bronze,  which  may have
            resulted in the  alteration of the  redeposited  copper  to cuprite  and partially to tenorite. This
            could also explain why the conservators  observed  this surface  feature  changing color, from  yel­
            low to red to purple, within a few months of the  re-treatment.



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