2005
DOI: 10.1016/j.ssi.2005.01.009
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A novel method for preparation of doped Ba3(Ca1.18Nb1.82)O9−δ: Application to ammonia synthesis at atmospheric pressure☆

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Cited by 78 publications
(45 citation statements)
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“…In the typical synthesis of LN powder, the first stage is to prepare fresh Nb 2 O 5 ·nH 2 O, which is used as the niobium source. The synthesis process was conducted as previously reported [12]. By a sol-gel method, citric acid was used as the complex reagent, which was added into the freshly precipitated niobic acid, in the molar ratio of [citric cid]:[Nb 5+ ] = 3:1.…”
Section: Synthesis Of Ln Powdermentioning
confidence: 99%
See 1 more Smart Citation
“…In the typical synthesis of LN powder, the first stage is to prepare fresh Nb 2 O 5 ·nH 2 O, which is used as the niobium source. The synthesis process was conducted as previously reported [12]. By a sol-gel method, citric acid was used as the complex reagent, which was added into the freshly precipitated niobic acid, in the molar ratio of [citric cid]:[Nb 5+ ] = 3:1.…”
Section: Synthesis Of Ln Powdermentioning
confidence: 99%
“…All of these undesirable characteristics limit its general application. Alternatively, niobic acid has been a promising candidate, because it is easily handled in an ambient atmosphere, is insensitive to moisture, is lower cost, and furthermore it can easily coordinate with ␣-carboxylic acid to form water-soluble [12]. Therefore, we develop a process stating from niobic acid as the Nb source to prepare LN powder.…”
Section: Introductionmentioning
confidence: 99%
“…In a typical synthesis of LN powders, the first stage was to prepare fresh Nb 2 O 5 ·nH 2 O, which was used as the niobium source. The synthesis process was conducted as previously reported [15]. Citric acid was added into the freshly precipitated niobic acid, in the molar ratio of [citric acid]:[Nb 5+ ] = 3:1.…”
Section: Synthesis Of Ln Powdersmentioning
confidence: 99%
“…Stoukides et al suggested [3] high temperature proton conducting (HTPC) materials can be used to synthesize ammonia by electrochemical methods in 1996 and subsequently the rates of evolution of ammonia of up to 10 −11 mol·cm −2 ·s −1 was obtained [4] . Our laboratory has developed the use of HTPC materials in the electrosynthesis of ammonia [5][6][7][8][9][10] and achieved rates of evolution of ammonia of up to 10 −9 mol·cm −2 ·s −1 . Using HTPC materials allowed ammonia synthesis to be realized at atmospheric pressure, but required relatively high temperatures at which ammonia started to decompose and thus restricted the yield of ammonia.…”
Section: Introductionmentioning
confidence: 99%