2015
DOI: 10.1016/j.corsci.2014.11.021
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Tracking the progression of bronze disease – A synchrotron X-ray diffraction study of nantokite hydrolysis

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Cited by 26 publications
(19 citation statements)
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“…It should be noted that cuprite layer on the surface of bronze is not completely stable. SEM measurements show that the corrosion product layer is relatively loose making it possible for the aggressive media to penetrate the layer reaching the cuprite/bronze interface, 42 especially after a long‐term immersion. In the case of weak acidity and in the presence of Cl − ions cuprite can dissolve forming CuCl2 40,43,44 : Cu2normalOgoodbreak+4Clgoodbreak+2H+0.5em0.5em2CuCl2goodbreak+H2normalO CuCl2 complex formed in the inner layer of corrosion products would diffuse into the bulk solution 33,45 .…”
Section: Discussionmentioning
confidence: 99%
“…It should be noted that cuprite layer on the surface of bronze is not completely stable. SEM measurements show that the corrosion product layer is relatively loose making it possible for the aggressive media to penetrate the layer reaching the cuprite/bronze interface, 42 especially after a long‐term immersion. In the case of weak acidity and in the presence of Cl − ions cuprite can dissolve forming CuCl2 40,43,44 : Cu2normalOgoodbreak+4Clgoodbreak+2H+0.5em0.5em2CuCl2goodbreak+H2normalO CuCl2 complex formed in the inner layer of corrosion products would diffuse into the bulk solution 33,45 .…”
Section: Discussionmentioning
confidence: 99%
“…Apparently, they had been exposed to a different corrosion environment from the others. Assuming that they were originally recovered with nantokite (CuCl) on the surface, the immersion in distilled water would have decomposed the nantokite, leaving cuprite behind which explains the lack of chlorine and the high oxygen level (Grayburn et al, 2015;MacLeod, 1981). Fig.…”
Section: Atomic Composition Datamentioning
confidence: 99%
“…The crystalline chemistry of the three surfaces is quite different as far as the balance of corrosion products present is concerned, which is expected in the case of the fully cleaned and conserved link MR81A1436, but which shows that the corrosion environment of MR82A6000 was different from that of MR81A2249. It is also worth remembering that very simple remedial treatment on recovery such as soaking in water can effectively remove chlorides and convert nantokite (CuCl) to cuprite (Cu 2 O) (Grayburn et al, 2015;Macleod, 1981), especially on small artefacts where there is no great thickness of metal to absorb seawater.…”
Section: Mr81a2249mentioning
confidence: 99%
“…This corrosion process is caused by the interaction between copper and chloride ions in presence of oxygen and at high relative humidity producing nantokite (CuCl) [2]. The formation of nantokite in the presence of air and moisture causes a cyclic corrosion process that produces a green powdery layer of copper hydroxychlorides Cu 2 (OH) 3 Cl on the artworks [3][4][5]. This corrosion product has three main polymorphic crystal forms: atacamite, clinoatacamite and botallackite [6].…”
Section: Introductionmentioning
confidence: 99%