2000
DOI: 10.1016/s0040-6031(00)00478-0
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Thermal stability and bonding in the silver complexes of ethylenediaminetetraacetic acid

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Cited by 20 publications
(20 citation statements)
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“…Silver neodecanoate's molecular structure resembles that of commonly used carboxylic acid-based dispersants, such as caprylic acid (CH 3 (CH 2 ) 6 COOH), lauric acid (CH 3 (CH 2 ) 10 COOH), or oleic acid (CH 3 (CH 2 ) 7 CHCH-(CH 2 ) 7 COOH), with the exception that the hydrogen atom of its carboxylic group is substituted with a silver atom through ionic bonding. 24 After it dissolves in α-terpineol, the silver neodecanoate behaves analogously to a capping agent when its silver atom is adsorbed onto the surface of a silver particle where a polymeric dispersant is not anchored. 25 In contrast, silver acetate cannot be added to such silver paste with the solid Figure 2 shows that the contact resistivity of silver paste without silver neodecanoate generally exhibited a parabolic behavior at peak firing temperatures from 750 to 830°C.…”
Section: Resultsmentioning
confidence: 99%
“…Silver neodecanoate's molecular structure resembles that of commonly used carboxylic acid-based dispersants, such as caprylic acid (CH 3 (CH 2 ) 6 COOH), lauric acid (CH 3 (CH 2 ) 10 COOH), or oleic acid (CH 3 (CH 2 ) 7 CHCH-(CH 2 ) 7 COOH), with the exception that the hydrogen atom of its carboxylic group is substituted with a silver atom through ionic bonding. 24 After it dissolves in α-terpineol, the silver neodecanoate behaves analogously to a capping agent when its silver atom is adsorbed onto the surface of a silver particle where a polymeric dispersant is not anchored. 25 In contrast, silver acetate cannot be added to such silver paste with the solid Figure 2 shows that the contact resistivity of silver paste without silver neodecanoate generally exhibited a parabolic behavior at peak firing temperatures from 750 to 830°C.…”
Section: Resultsmentioning
confidence: 99%
“…To synthesize the silver oxalate, 2.00 g silver nitrate (!99.0%, Sigma Aldrich) was dissolved in 20 mL milliQ water and added to oxalic acid solution at 60°C. The latter solution was obtained by dissolving 1.48 g oxalic acid dihydrate (99%, Sigma Aldrich) (2:1 M ratio) in 40 mL milliQ water at 60°C [50][51][52]. Silver oxalate started to precipitate immediately, and was obtained after centrifugation and three times washing with milliQ water and once with ethanol.…”
Section: Silver Precursormentioning
confidence: 99%
“…Since the 1970's there have been a number of mechanistic studies of the formation of alkyl radicals through the pyrolytic decarboxylation of silver carboxylates, RCO 2 Ag [20][21][22][23][24], and various R groups have been employed; for example, Karpova et al,studied trifluoroacetates [24]. Fritz and Hiemeyer [25] showed that if trifluoroacetate pyrolysis is carried out in the presence of fullerenes then addition of CF 3 groups to the fullerene cage occurs, and this has been studied in detail more recently [26][27][28].…”
Section: Introductionmentioning
confidence: 99%