Model apatite systems for the stabilization of toxic metals : I, calcium lead vanadate

Apatites of composition (Ca10−xPbx)(VO4)6F2 with 0 ≤x≤ 9 were synthesized by sintering in air at 800°C the oxides of calcium, lead, and vanadium that were mixed with calcium fluoride. Variations in lattice parameters, grain size, and durability were monitored as a function of composition. The expect...

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Main Authors: Dong, Zhili, White, Timothy John, Wei, Bing, Laursen, Karin
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2013
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Online Access:https://hdl.handle.net/10356/95671
http://hdl.handle.net/10220/9477
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spelling sg-ntu-dr.10356-956712023-07-14T15:53:59Z Model apatite systems for the stabilization of toxic metals : I, calcium lead vanadate Dong, Zhili White, Timothy John Wei, Bing Laursen, Karin School of Materials Science & Engineering DRNTU::Engineering::Materials Apatites of composition (Ca10−xPbx)(VO4)6F2 with 0 ≤x≤ 9 were synthesized by sintering in air at 800°C the oxides of calcium, lead, and vanadium that were mixed with calcium fluoride. Variations in lattice parameters, grain size, and durability were monitored as a function of composition. The expected dilation in unit cell edges with increasing replacement of calcium (IR = 1.26 Å) by lead (IR = 1.45 Å) was observed. The a cell edge (in angstroms) varied linearly (0.0458 x+ 9.7068) with x, while c followed the binomial function 0.0018x2+ 0.0279x+ 7.0118. Average grain sizes increased from approximately 5 μm (x= 0) to 25 μm (x= 9) as grain growth was enhanced due to incipient melting of the lead-rich compositions. For x < 5 the materials were biphasic. Overall dissolution, as determined by the toxicity characteristic leaching procedure (TCLP), was faster in calcium-rich apatites. Etching of well-crystallized apatite grains occurred preferentially on {1010} faces. These leach losses were augmented through the more rapid removal of cryptocrystalline regions and intergranular thin films. Accepted version 2013-04-10T08:18:01Z 2019-12-06T19:19:31Z 2013-04-10T08:18:01Z 2019-12-06T19:19:31Z 2002 2002 Journal Article Dong, Z., White, T. J., Wei, B., & Laursen, K. (2002). Model Apatite Systems for the Stabilization of Toxic Metals: I, Calcium Lead Vanadate. Journal of the American Ceramic Society, 85(10), 2515-2522. 0002-7820 https://hdl.handle.net/10356/95671 http://hdl.handle.net/10220/9477 10.1111/j.1151-2916.2002.tb00489.x en Journal of the American ceramic society © 2002 The American Ceramic Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Journal of the American Ceramic Society, The American Ceramic Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1111/j.1151-2916.2002.tb00489.x ]. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Engineering::Materials
spellingShingle DRNTU::Engineering::Materials
Dong, Zhili
White, Timothy John
Wei, Bing
Laursen, Karin
Model apatite systems for the stabilization of toxic metals : I, calcium lead vanadate
description Apatites of composition (Ca10−xPbx)(VO4)6F2 with 0 ≤x≤ 9 were synthesized by sintering in air at 800°C the oxides of calcium, lead, and vanadium that were mixed with calcium fluoride. Variations in lattice parameters, grain size, and durability were monitored as a function of composition. The expected dilation in unit cell edges with increasing replacement of calcium (IR = 1.26 Å) by lead (IR = 1.45 Å) was observed. The a cell edge (in angstroms) varied linearly (0.0458 x+ 9.7068) with x, while c followed the binomial function 0.0018x2+ 0.0279x+ 7.0118. Average grain sizes increased from approximately 5 μm (x= 0) to 25 μm (x= 9) as grain growth was enhanced due to incipient melting of the lead-rich compositions. For x < 5 the materials were biphasic. Overall dissolution, as determined by the toxicity characteristic leaching procedure (TCLP), was faster in calcium-rich apatites. Etching of well-crystallized apatite grains occurred preferentially on {1010} faces. These leach losses were augmented through the more rapid removal of cryptocrystalline regions and intergranular thin films.
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Dong, Zhili
White, Timothy John
Wei, Bing
Laursen, Karin
format Article
author Dong, Zhili
White, Timothy John
Wei, Bing
Laursen, Karin
author_sort Dong, Zhili
title Model apatite systems for the stabilization of toxic metals : I, calcium lead vanadate
title_short Model apatite systems for the stabilization of toxic metals : I, calcium lead vanadate
title_full Model apatite systems for the stabilization of toxic metals : I, calcium lead vanadate
title_fullStr Model apatite systems for the stabilization of toxic metals : I, calcium lead vanadate
title_full_unstemmed Model apatite systems for the stabilization of toxic metals : I, calcium lead vanadate
title_sort model apatite systems for the stabilization of toxic metals : i, calcium lead vanadate
publishDate 2013
url https://hdl.handle.net/10356/95671
http://hdl.handle.net/10220/9477
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