2009
DOI: 10.3363/prb.23.20
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Synthesis and Electrical Conductivity of Tetra-Valent Cerium Polyphosphate Bulks

Abstract: Tetra-valent cerium phosphate was synthesized from cerium oxide and phosphoric acid by heating. The sintering processes, pressure-less sintering (PLS), spark plasma sintering (SPS), and hydrothermal hot pressing (HHP), were tried to obtain polyphosphate bulks. Furthermore, the electrical conductivity of cerium polyphosphate bulks was investigated. Tetra-valent cerium phosphate was synthesized by heating at 700ºC for 20 hours. The hydrothermal hot pressing process was the suitable method to synthesize the tetra… Show more

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Cited by 16 publications
(20 citation statements)
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“…The filling factor is approximately 70%, which is calculated from the ideal density of lanthanum polyphosphate. This percentage is lower than that of the phosphate bulk samples synthesized by the HHP process in the previous experiments [8][9][10]. The low filling factor can potentially absorb the physical stress.…”
Section: Density Of Bulk Lanthanum Polyphosphatesmentioning
confidence: 60%
“…The filling factor is approximately 70%, which is calculated from the ideal density of lanthanum polyphosphate. This percentage is lower than that of the phosphate bulk samples synthesized by the HHP process in the previous experiments [8][9][10]. The low filling factor can potentially absorb the physical stress.…”
Section: Density Of Bulk Lanthanum Polyphosphatesmentioning
confidence: 60%
“…Only a conventional calcination technique has been used to prepare CeP 2 O 7 and Ce(PO 3 ) 4 in previous studies [3,7,8,15,[29][30][31] 4 were adequately mixed in an agate mortar. The mixture was stored in a porcelain crucible with an insulation layer and directly irradiated at various MW powers for different times.…”
Section: ) On U(vi)mentioning
confidence: 99%
“…CeP 2 O 7 powder can reportedly be obtained by the dehydration of Ce(HPO 4 ) 2 ÁxH 2 O, which was prepared by heating H 3 PO 4 and Ce(SO 4 ) 2 ÁxH 2 O under reflux conditions, using a heat treatment at 600°C for 16 h. CeO 2 and 85 % H 3PO 4 have also been calcined at 300°C for 8 h[3], or at 700°C for 20 h[29]. Amorphous CeP 2 O 7 powder has been obtained as well using Ce(SO 4 ) 2 Á4H 2 O and Na 4 P 2 O 7 as initial materials at 80°C for 24 h; crystallization from the amorphous phase occurred at around 500°C to form crystalline cerium pyrophosphate[30].…”
mentioning
confidence: 99%
“…(Shuetz & Caruso, 2002;Meiser et al, 2004). The condensed phosphates have different properties from those of orthophosphates and can therefore be used as novel functional materials , Onoda et al, 2005Briche et al, 2010;Onoda et al, 2010).…”
Section: Introducationmentioning
confidence: 99%