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Phase stability and rapid consolidation of hydroxyapatite-zirconia nano-coprecipitates made using continuous hydrothermal flow synthesis

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Phase stability and rapid consolidation of hydroxyapatite-zirconia nano-coprecipitates made using continuous hydrothermal flow synthesis. / Chaudhry, A.A.; Yan, H.; Viola, G. et al.
In: JOURNAL OF BIOMATERIALS APPLICATIONS, Vol. 27, No. 1, 2012, p. 79-90.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Chaudhry, AA, Yan, H, Viola, G, Reece, MJ, Knowles, JC, Gong, K, Rehman, I & Darr, JA 2012, 'Phase stability and rapid consolidation of hydroxyapatite-zirconia nano-coprecipitates made using continuous hydrothermal flow synthesis', JOURNAL OF BIOMATERIALS APPLICATIONS, vol. 27, no. 1, pp. 79-90. https://doi.org/10.1177/0885328212444483

APA

Chaudhry, A. A., Yan, H., Viola, G., Reece, M. J., Knowles, J. C., Gong, K., Rehman, I., & Darr, J. A. (2012). Phase stability and rapid consolidation of hydroxyapatite-zirconia nano-coprecipitates made using continuous hydrothermal flow synthesis. JOURNAL OF BIOMATERIALS APPLICATIONS, 27(1), 79-90. https://doi.org/10.1177/0885328212444483

Vancouver

Chaudhry AA, Yan H, Viola G, Reece MJ, Knowles JC, Gong K et al. Phase stability and rapid consolidation of hydroxyapatite-zirconia nano-coprecipitates made using continuous hydrothermal flow synthesis. JOURNAL OF BIOMATERIALS APPLICATIONS. 2012;27(1):79-90. doi: 10.1177/0885328212444483

Author

Chaudhry, A.A. ; Yan, H. ; Viola, G. et al. / Phase stability and rapid consolidation of hydroxyapatite-zirconia nano-coprecipitates made using continuous hydrothermal flow synthesis. In: JOURNAL OF BIOMATERIALS APPLICATIONS. 2012 ; Vol. 27, No. 1. pp. 79-90.

Bibtex

@article{91801dd816be4e7daca3250e2d5a0dd9,
title = "Phase stability and rapid consolidation of hydroxyapatite-zirconia nano-coprecipitates made using continuous hydrothermal flow synthesis",
abstract = "A rapid and continuous hydrothermal route for the synthesis of nano-sized hydroxyapatite rods co-precipitated with calcium-doped zirconia nanoparticles using a superheated water flow at 450°C and 24.1MPa as a crystallizing medium is described. Hydroxyapatite and calcium-doped zirconia phases in the powder mixtures could be clearly identified based on particle size and morphology under transmission electron microscopy. Retention of a nanostructure after sintering is crucial to load-bearing applications of hydroxyapatite-based ceramics. Therefore, rapid consolidation of the co-precipitates was investigated using a spark plasma sintering furnace under a range of processing conditions. Samples nominally containing 5 and 10wt% calcium-doped zirconia and hydroxyapatite made with Ca:P solution molar ratio 2.5 showed excellent thermal stability (investigated using in situ variable temperature X-ray diffraction) and were sintered via spark plasma sintering to >96% sintered densities at 1000°C resulting in hydroxyapatite and calcium-doped zirconia as the only two phases. Mechanical tests of spark plasma sintering sintered samples (containing 10wt% calcium-doped zirconia) revealed a three-pt flexural strength of 107.7MPa and Weibull modulus of 9.9. The complementary nature of the spark plasma sintering technique and continuous hydrothermal flow synthesis (which results in retention of a nanostructure even after sintering at elevated temperatures) was hence showcased. {\textcopyright} The Author(s) 2012 Reprints and permissions.",
keywords = "hydrothermal flow, Hydroxyapatite, nanostructure, spark plasma sintering, zirconia, Co-precipitated, Co-precipitates, Elevated temperature, Flow synthesis, Hydrothermal routes, In-situ, Load-bearing, Mechanical tests, Molar ratio, Nano-sized hydroxyapatite, Particle size and morphologies, Powder mixtures, Processing condition, Sintered density, Sintered samples, Spark plasma, Superheated water, Variable temperature, Weibull modulus, Zirconia nanoparticles, Calcium, Hydrothermal synthesis, Nanostructures, Phase stability, Spark plasma sintering, Transmission electron microscopy, Weibull distribution, X ray diffraction, Zirconia, hydroxyapatite, nanoparticle, zirconium, zirconium oxide, article, chemistry, particle size, powder diffraction, scanning electron microscopy, transmission electron microscopy, Durapatite, Microscopy, Electron, Scanning, Microscopy, Electron, Transmission, Nanoparticles, Particle Size, Powder Diffraction, Zirconium",
author = "A.A. Chaudhry and H. Yan and G. Viola and M.J. Reece and J.C. Knowles and K. Gong and I. Rehman and J.A. Darr",
year = "2012",
doi = "10.1177/0885328212444483",
language = "English",
volume = "27",
pages = "79--90",
journal = "JOURNAL OF BIOMATERIALS APPLICATIONS",
issn = "0885-3282",
publisher = "SAGE Publications Ltd",
number = "1",

}

RIS

TY - JOUR

T1 - Phase stability and rapid consolidation of hydroxyapatite-zirconia nano-coprecipitates made using continuous hydrothermal flow synthesis

AU - Chaudhry, A.A.

AU - Yan, H.

AU - Viola, G.

AU - Reece, M.J.

AU - Knowles, J.C.

AU - Gong, K.

AU - Rehman, I.

AU - Darr, J.A.

PY - 2012

Y1 - 2012

N2 - A rapid and continuous hydrothermal route for the synthesis of nano-sized hydroxyapatite rods co-precipitated with calcium-doped zirconia nanoparticles using a superheated water flow at 450°C and 24.1MPa as a crystallizing medium is described. Hydroxyapatite and calcium-doped zirconia phases in the powder mixtures could be clearly identified based on particle size and morphology under transmission electron microscopy. Retention of a nanostructure after sintering is crucial to load-bearing applications of hydroxyapatite-based ceramics. Therefore, rapid consolidation of the co-precipitates was investigated using a spark plasma sintering furnace under a range of processing conditions. Samples nominally containing 5 and 10wt% calcium-doped zirconia and hydroxyapatite made with Ca:P solution molar ratio 2.5 showed excellent thermal stability (investigated using in situ variable temperature X-ray diffraction) and were sintered via spark plasma sintering to >96% sintered densities at 1000°C resulting in hydroxyapatite and calcium-doped zirconia as the only two phases. Mechanical tests of spark plasma sintering sintered samples (containing 10wt% calcium-doped zirconia) revealed a three-pt flexural strength of 107.7MPa and Weibull modulus of 9.9. The complementary nature of the spark plasma sintering technique and continuous hydrothermal flow synthesis (which results in retention of a nanostructure even after sintering at elevated temperatures) was hence showcased. © The Author(s) 2012 Reprints and permissions.

AB - A rapid and continuous hydrothermal route for the synthesis of nano-sized hydroxyapatite rods co-precipitated with calcium-doped zirconia nanoparticles using a superheated water flow at 450°C and 24.1MPa as a crystallizing medium is described. Hydroxyapatite and calcium-doped zirconia phases in the powder mixtures could be clearly identified based on particle size and morphology under transmission electron microscopy. Retention of a nanostructure after sintering is crucial to load-bearing applications of hydroxyapatite-based ceramics. Therefore, rapid consolidation of the co-precipitates was investigated using a spark plasma sintering furnace under a range of processing conditions. Samples nominally containing 5 and 10wt% calcium-doped zirconia and hydroxyapatite made with Ca:P solution molar ratio 2.5 showed excellent thermal stability (investigated using in situ variable temperature X-ray diffraction) and were sintered via spark plasma sintering to >96% sintered densities at 1000°C resulting in hydroxyapatite and calcium-doped zirconia as the only two phases. Mechanical tests of spark plasma sintering sintered samples (containing 10wt% calcium-doped zirconia) revealed a three-pt flexural strength of 107.7MPa and Weibull modulus of 9.9. The complementary nature of the spark plasma sintering technique and continuous hydrothermal flow synthesis (which results in retention of a nanostructure even after sintering at elevated temperatures) was hence showcased. © The Author(s) 2012 Reprints and permissions.

KW - hydrothermal flow

KW - Hydroxyapatite

KW - nanostructure

KW - spark plasma sintering

KW - zirconia

KW - Co-precipitated

KW - Co-precipitates

KW - Elevated temperature

KW - Flow synthesis

KW - Hydrothermal routes

KW - In-situ

KW - Load-bearing

KW - Mechanical tests

KW - Molar ratio

KW - Nano-sized hydroxyapatite

KW - Particle size and morphologies

KW - Powder mixtures

KW - Processing condition

KW - Sintered density

KW - Sintered samples

KW - Spark plasma

KW - Superheated water

KW - Variable temperature

KW - Weibull modulus

KW - Zirconia nanoparticles

KW - Calcium

KW - Hydrothermal synthesis

KW - Nanostructures

KW - Phase stability

KW - Spark plasma sintering

KW - Transmission electron microscopy

KW - Weibull distribution

KW - X ray diffraction

KW - Zirconia

KW - hydroxyapatite

KW - nanoparticle

KW - zirconium

KW - zirconium oxide

KW - article

KW - chemistry

KW - particle size

KW - powder diffraction

KW - scanning electron microscopy

KW - transmission electron microscopy

KW - Durapatite

KW - Microscopy, Electron, Scanning

KW - Microscopy, Electron, Transmission

KW - Nanoparticles

KW - Particle Size

KW - Powder Diffraction

KW - Zirconium

U2 - 10.1177/0885328212444483

DO - 10.1177/0885328212444483

M3 - Journal article

VL - 27

SP - 79

EP - 90

JO - JOURNAL OF BIOMATERIALS APPLICATIONS

JF - JOURNAL OF BIOMATERIALS APPLICATIONS

SN - 0885-3282

IS - 1

ER -