A physical approach to modify the hydraulic reactivity of α-tricalcium phosphate powder
A microsized α-tricalcium phosphate (α-TCP) powder was calcined at various temperatures (350 °C < T < 800 °C) for various durations (1–24 h) and the resulting physico-chemical and reactivity changes were measured. Without calcination, the α-TCP powder started reacting within minutes after cont...
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creator | Bohner, Marc Luginbühl, Reto Reber, Christian Doebelin, Nicola Baroud, Gamal Conforto, Egle |
description | A microsized α-tricalcium phosphate (α-TCP) powder was calcined at various temperatures (350
°C
<
T
<
800
°C) for various durations (1–24
h) and the resulting physico-chemical and reactivity changes were measured. Without calcination, the α-TCP powder started reacting within minutes after contacting a 0.2
M Na
2HPO
4 solution as measured by isothermal calorimetry. The overall reaction was finished within a few days. After calcination at 350
°C
⩽
T
⩽
550
°C for 24
h, no significant changes in the crystalline composition, crystallite size, particle size or specific surface area were noticed. However, the powder reactivity was progressively changed. More specifically, the hydraulic reaction of the powders calcined at 500 and 550
°C only started after 2–3
h whereas the overall hydraulic reaction was only slightly postponed, suggesting that physical or chemical changes had occurred at the particle surface. As mainly physical changes were detected at the particle surface during calcination at 500
°C, it was speculated that the appearance of this reaction delay (=
induction time) was due to the disappearance of surface defects during the calcination step, i.e. to the need to create surface defects to induce dissolution and hence reaction. |
doi_str_mv | 10.1016/j.actbio.2009.05.024 |
format | Article |
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°C
<
T
<
800
°C) for various durations (1–24
h) and the resulting physico-chemical and reactivity changes were measured. Without calcination, the α-TCP powder started reacting within minutes after contacting a 0.2
M Na
2HPO
4 solution as measured by isothermal calorimetry. The overall reaction was finished within a few days. After calcination at 350
°C
⩽
T
⩽
550
°C for 24
h, no significant changes in the crystalline composition, crystallite size, particle size or specific surface area were noticed. However, the powder reactivity was progressively changed. More specifically, the hydraulic reaction of the powders calcined at 500 and 550
°C only started after 2–3
h whereas the overall hydraulic reaction was only slightly postponed, suggesting that physical or chemical changes had occurred at the particle surface. As mainly physical changes were detected at the particle surface during calcination at 500
°C, it was speculated that the appearance of this reaction delay (=
induction time) was due to the disappearance of surface defects during the calcination step, i.e. to the need to create surface defects to induce dissolution and hence reaction.</description><identifier>ISSN: 1742-7061</identifier><identifier>EISSN: 1878-7568</identifier><identifier>DOI: 10.1016/j.actbio.2009.05.024</identifier><identifier>PMID: 19470412</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Biomaterials ; Calcium phosphate cement ; Calcium Phosphates - chemistry ; Calorimetry - methods ; Hydroxyapatite ; Isothermal calorimetry ; Materials Testing ; Particle Size ; Powders - chemistry ; Solutions ; Temperature ; Thermodynamics ; X-Ray Diffraction ; α-Tricalcium phosphate</subject><ispartof>Acta biomaterialia, 2009-11, Vol.5 (9), p.3524-3535</ispartof><rights>2009 Acta Materialia Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-9561cef8b56609dd8cec4aa712e2b784a6c1917b55f757da5a03d2e4ae05d3573</citedby><cites>FETCH-LOGICAL-c392t-9561cef8b56609dd8cec4aa712e2b784a6c1917b55f757da5a03d2e4ae05d3573</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1742706109002384$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19470412$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bohner, Marc</creatorcontrib><creatorcontrib>Luginbühl, Reto</creatorcontrib><creatorcontrib>Reber, Christian</creatorcontrib><creatorcontrib>Doebelin, Nicola</creatorcontrib><creatorcontrib>Baroud, Gamal</creatorcontrib><creatorcontrib>Conforto, Egle</creatorcontrib><title>A physical approach to modify the hydraulic reactivity of α-tricalcium phosphate powder</title><title>Acta biomaterialia</title><addtitle>Acta Biomater</addtitle><description>A microsized α-tricalcium phosphate (α-TCP) powder was calcined at various temperatures (350
°C
<
T
<
800
°C) for various durations (1–24
h) and the resulting physico-chemical and reactivity changes were measured. Without calcination, the α-TCP powder started reacting within minutes after contacting a 0.2
M Na
2HPO
4 solution as measured by isothermal calorimetry. The overall reaction was finished within a few days. After calcination at 350
°C
⩽
T
⩽
550
°C for 24
h, no significant changes in the crystalline composition, crystallite size, particle size or specific surface area were noticed. However, the powder reactivity was progressively changed. More specifically, the hydraulic reaction of the powders calcined at 500 and 550
°C only started after 2–3
h whereas the overall hydraulic reaction was only slightly postponed, suggesting that physical or chemical changes had occurred at the particle surface. As mainly physical changes were detected at the particle surface during calcination at 500
°C, it was speculated that the appearance of this reaction delay (=
induction time) was due to the disappearance of surface defects during the calcination step, i.e. to the need to create surface defects to induce dissolution and hence reaction.</description><subject>Biomaterials</subject><subject>Calcium phosphate cement</subject><subject>Calcium Phosphates - chemistry</subject><subject>Calorimetry - methods</subject><subject>Hydroxyapatite</subject><subject>Isothermal calorimetry</subject><subject>Materials Testing</subject><subject>Particle Size</subject><subject>Powders - chemistry</subject><subject>Solutions</subject><subject>Temperature</subject><subject>Thermodynamics</subject><subject>X-Ray Diffraction</subject><subject>α-Tricalcium phosphate</subject><issn>1742-7061</issn><issn>1878-7568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMGK1TAUhosozjj6BiJZ6ar1JE2aZCMMgzoDA24U3IU0OaW5tJOatCN9LF_EZzKXe8HdrM5ZfP9_Dl9VvaXQUKDdx0Nj3dqH2DAA3YBogPFn1SVVUtVSdOp52SVntYSOXlSvcj4AtIoy9bK6oJpL4JRdVj-vyTLuOTg7EbssKVo3kjWSOfow7GQdkYy7T3abgiMJy8nwGNadxIH8_VOv6Rh0YZtLS8zLaFckS_ztMb2uXgx2yvjmPK-qH18-f7-5re-_fb27ub6vXavZWmvRUYeD6kXXgfZeOXTcWkkZsl4qbjtHNZW9EIMU0lthofUMuUUQvhWyvao-nHrL7782zKuZQ3Y4TfYB45aNbDlo4FoX8v2TJKOggEpWQH4CXYo5JxzMksJs024omKN7czAn9-bo3oAwxX2JvTv3b_2M_n_oLLsAn04AFh-PAZPJLuCDQx8SutX4GJ6-8A_r95iB</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Bohner, Marc</creator><creator>Luginbühl, Reto</creator><creator>Reber, Christian</creator><creator>Doebelin, Nicola</creator><creator>Baroud, Gamal</creator><creator>Conforto, Egle</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20091101</creationdate><title>A physical approach to modify the hydraulic reactivity of α-tricalcium phosphate powder</title><author>Bohner, Marc ; Luginbühl, Reto ; Reber, Christian ; Doebelin, Nicola ; Baroud, Gamal ; Conforto, Egle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-9561cef8b56609dd8cec4aa712e2b784a6c1917b55f757da5a03d2e4ae05d3573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Biomaterials</topic><topic>Calcium phosphate cement</topic><topic>Calcium Phosphates - chemistry</topic><topic>Calorimetry - methods</topic><topic>Hydroxyapatite</topic><topic>Isothermal calorimetry</topic><topic>Materials Testing</topic><topic>Particle Size</topic><topic>Powders - chemistry</topic><topic>Solutions</topic><topic>Temperature</topic><topic>Thermodynamics</topic><topic>X-Ray Diffraction</topic><topic>α-Tricalcium phosphate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bohner, Marc</creatorcontrib><creatorcontrib>Luginbühl, Reto</creatorcontrib><creatorcontrib>Reber, Christian</creatorcontrib><creatorcontrib>Doebelin, Nicola</creatorcontrib><creatorcontrib>Baroud, Gamal</creatorcontrib><creatorcontrib>Conforto, Egle</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Acta biomaterialia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bohner, Marc</au><au>Luginbühl, Reto</au><au>Reber, Christian</au><au>Doebelin, Nicola</au><au>Baroud, Gamal</au><au>Conforto, Egle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A physical approach to modify the hydraulic reactivity of α-tricalcium phosphate powder</atitle><jtitle>Acta biomaterialia</jtitle><addtitle>Acta Biomater</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>5</volume><issue>9</issue><spage>3524</spage><epage>3535</epage><pages>3524-3535</pages><issn>1742-7061</issn><eissn>1878-7568</eissn><abstract>A microsized α-tricalcium phosphate (α-TCP) powder was calcined at various temperatures (350
°C
<
T
<
800
°C) for various durations (1–24
h) and the resulting physico-chemical and reactivity changes were measured. Without calcination, the α-TCP powder started reacting within minutes after contacting a 0.2
M Na
2HPO
4 solution as measured by isothermal calorimetry. The overall reaction was finished within a few days. After calcination at 350
°C
⩽
T
⩽
550
°C for 24
h, no significant changes in the crystalline composition, crystallite size, particle size or specific surface area were noticed. However, the powder reactivity was progressively changed. More specifically, the hydraulic reaction of the powders calcined at 500 and 550
°C only started after 2–3
h whereas the overall hydraulic reaction was only slightly postponed, suggesting that physical or chemical changes had occurred at the particle surface. As mainly physical changes were detected at the particle surface during calcination at 500
°C, it was speculated that the appearance of this reaction delay (=
induction time) was due to the disappearance of surface defects during the calcination step, i.e. to the need to create surface defects to induce dissolution and hence reaction.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>19470412</pmid><doi>10.1016/j.actbio.2009.05.024</doi><tpages>12</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Biomaterials Calcium phosphate cement Calcium Phosphates - chemistry Calorimetry - methods Hydroxyapatite Isothermal calorimetry Materials Testing Particle Size Powders - chemistry Solutions Temperature Thermodynamics X-Ray Diffraction α-Tricalcium phosphate |
title | A physical approach to modify the hydraulic reactivity of α-tricalcium phosphate powder |
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