1997
DOI: 10.2138/am-1997-5-610
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Incorporation of rare earth elements in titanite; stabilization of the A2/a dimorph by creation of antiphase boundaries

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Cited by 36 publications
(22 citation statements)
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“…Concerning titanite crystals, the results reported in Table 2 show that this crystalline phase is the only one able to incorporate trivalent lanthanide ions (Ln 3+ ) in the surface crystallized layer. It appears that Ln 3+ ions are only incorporated into the calcium site of the titanite structure (there is only one type of calcium site in this structure and this site is 7-fold coordinated with oxygen ions [78]) probably because the tetrahedral silicon and the octahedral titanium sites are too small. This result is in accordance with the one published by Higgins et al for natural titanite samples [79].…”
Section: Tablementioning
confidence: 93%
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“…Concerning titanite crystals, the results reported in Table 2 show that this crystalline phase is the only one able to incorporate trivalent lanthanide ions (Ln 3+ ) in the surface crystallized layer. It appears that Ln 3+ ions are only incorporated into the calcium site of the titanite structure (there is only one type of calcium site in this structure and this site is 7-fold coordinated with oxygen ions [78]) probably because the tetrahedral silicon and the octahedral titanium sites are too small. This result is in accordance with the one published by Higgins et al for natural titanite samples [79].…”
Section: Tablementioning
confidence: 93%
“…As indicated above, tetravalent cerium ions are preferentially incorporated in the baddeleyite (ZrO 2 ) crystals. Divalent europium, that was detected by ESR in the parent glass GEu [13], is also una- Table 4 Sum of the bond valences (Rs Lnj ) calculated for the different lanthanide (Ln) in the calcium site of titanite (coordination j = 7) using the crystallographic structural data of Hughes et al [78] and the R 0 values taken from [71]. V Ln is Ln oxidation state.…”
Section: Tablementioning
confidence: 99%
“…160-1930 ppm) and low REE concentrations (b200 ppm); and sample Tit-E was found to be rich in both, Cr and REE (see Table 1). Chromium and other metals, such as Nb, Ta, V, Mn, Mg, Sn, Al, and Fe, are generally considered to be incorporated at the six-fold coordinated Ti-site (Higgins and Ribbe, 1976;Fleischer, 1978), whereas REEs substitute Ca on its large, sevencoordinated site (Hughes et al, 1997). Charge-balance of trivalent REE within the titanite structure is explained by a coupled substitution with Al and Fe (e.g., Che et al, 2013):…”
Section: Titanite -Catisiomentioning
confidence: 99%
“…Both lead to domain wall pinning suppressing an enlargement of small P2 1 /c domains around 500 K and prevent the establishment of long-range order. For that reason the average space group for titanite is C2/c even at room-temperature and locally the P2 1 /c symmetry is still preserved in the crystalline domains [1,[54][55][56].…”
Section: Temperature Induced Phase Transition In Partially Amorphous mentioning
confidence: 99%