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Effect of Ti ion substitution on the structure of hydroxylapatite
In order to increase the understanding of the interaction of titanium (Ti) ions with hydroxylapatite (HA) structure, two different kinds of experiments were carried out. In the first, titanium ion containing HA was made via a precipitation method. Tetraethyl orthotitanate were added to precipitating...
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Published in: | Journal of the European Ceramic Society 2008, Vol.28 (11), p.2137-2149 |
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description | In order to increase the understanding of the interaction of titanium (Ti) ions with hydroxylapatite (HA) structure, two different kinds of experiments were carried out. In the first, titanium ion containing HA was made via a precipitation method. Tetraethyl orthotitanate were added to precipitating HA to incorporate Ti ions into HA structure. The precipitates were dried and sintered in air at 500
°C, 700
°C, 900
°C, 1100
°C, and 1300
°C for 2
h. X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy analysis were used to characterize the samples. In the second, rather as the complementary experiments to the first set, powder mixtures of HA/CaTiO
3, tri-calcium phosphate/CaTiO
3 were sintered in air at 900
°C, 1100
°C, and 1300
°C for 2
h, and characterized with X-ray diffraction technique. Lattice parameters from X-ray diffraction spectra showed that Ti incorporation into the apatite structure caused lattice shrinkage. The grain sizes of substituted HAs were smaller than those of pure HA. Increasing the amount of the Ti ions in HA caused the decomposition of HA associated with the formation of α-tricalcium phosphate and CaTiO
3. This enhanced the porosity in titanium containing HA compared to pure HA. As also verified by the results of complementary experiments, α-tricalcium phosphate (TCP) and CaTiO
3 reacted at 1300
°C in the expense of both phases in the presence of HA. No reaction products in the form of new phases could be identified. On the other hand, the same reaction was not observed in the samples that did not have stable HA phase. |
doi_str_mv | 10.1016/j.jeurceramsoc.2008.03.007 |
format | article |
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°C, 700
°C, 900
°C, 1100
°C, and 1300
°C for 2
h. X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy analysis were used to characterize the samples. In the second, rather as the complementary experiments to the first set, powder mixtures of HA/CaTiO
3, tri-calcium phosphate/CaTiO
3 were sintered in air at 900
°C, 1100
°C, and 1300
°C for 2
h, and characterized with X-ray diffraction technique. Lattice parameters from X-ray diffraction spectra showed that Ti incorporation into the apatite structure caused lattice shrinkage. The grain sizes of substituted HAs were smaller than those of pure HA. Increasing the amount of the Ti ions in HA caused the decomposition of HA associated with the formation of α-tricalcium phosphate and CaTiO
3. This enhanced the porosity in titanium containing HA compared to pure HA. As also verified by the results of complementary experiments, α-tricalcium phosphate (TCP) and CaTiO
3 reacted at 1300
°C in the expense of both phases in the presence of HA. No reaction products in the form of new phases could be identified. On the other hand, the same reaction was not observed in the samples that did not have stable HA phase.</description><identifier>ISSN: 0955-2219</identifier><identifier>EISSN: 1873-619X</identifier><identifier>DOI: 10.1016/j.jeurceramsoc.2008.03.007</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Apatite ; Applied sciences ; Biological and medical sciences ; Building materials. Ceramics. Glasses ; CaTiO 3 ; Ceramic industries ; Chemical industry and chemicals ; Exact sciences and technology ; Medical sciences ; Miscellaneous ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; Sintering ; Technical ceramics ; Technology. Biomaterials. Equipments. Material. Instrumentation ; Titanium substitution ; Tri-calcium phosphate</subject><ispartof>Journal of the European Ceramic Society, 2008, Vol.28 (11), p.2137-2149</ispartof><rights>2008 Elsevier Ltd</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-5d7a9392a8729aca47699d36fad27a6515bd1a78b0db422c787f20836a4878263</citedby><cites>FETCH-LOGICAL-c451t-5d7a9392a8729aca47699d36fad27a6515bd1a78b0db422c787f20836a4878263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4021,27921,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20430756$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Ergun, Celaletdin</creatorcontrib><title>Effect of Ti ion substitution on the structure of hydroxylapatite</title><title>Journal of the European Ceramic Society</title><description>In order to increase the understanding of the interaction of titanium (Ti) ions with hydroxylapatite (HA) structure, two different kinds of experiments were carried out. In the first, titanium ion containing HA was made via a precipitation method. Tetraethyl orthotitanate were added to precipitating HA to incorporate Ti ions into HA structure. The precipitates were dried and sintered in air at 500
°C, 700
°C, 900
°C, 1100
°C, and 1300
°C for 2
h. X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy analysis were used to characterize the samples. In the second, rather as the complementary experiments to the first set, powder mixtures of HA/CaTiO
3, tri-calcium phosphate/CaTiO
3 were sintered in air at 900
°C, 1100
°C, and 1300
°C for 2
h, and characterized with X-ray diffraction technique. Lattice parameters from X-ray diffraction spectra showed that Ti incorporation into the apatite structure caused lattice shrinkage. The grain sizes of substituted HAs were smaller than those of pure HA. Increasing the amount of the Ti ions in HA caused the decomposition of HA associated with the formation of α-tricalcium phosphate and CaTiO
3. This enhanced the porosity in titanium containing HA compared to pure HA. As also verified by the results of complementary experiments, α-tricalcium phosphate (TCP) and CaTiO
3 reacted at 1300
°C in the expense of both phases in the presence of HA. No reaction products in the form of new phases could be identified. On the other hand, the same reaction was not observed in the samples that did not have stable HA phase.</description><subject>Apatite</subject><subject>Applied sciences</subject><subject>Biological and medical sciences</subject><subject>Building materials. Ceramics. Glasses</subject><subject>CaTiO 3</subject><subject>Ceramic industries</subject><subject>Chemical industry and chemicals</subject><subject>Exact sciences and technology</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>Sintering</subject><subject>Technical ceramics</subject><subject>Technology. Biomaterials. Equipments. Material. Instrumentation</subject><subject>Titanium substitution</subject><subject>Tri-calcium phosphate</subject><issn>0955-2219</issn><issn>1873-619X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqNkFtLwzAUgIMoOKf_oQj61nqStE3i25jzAgNfJvgWTtOUZXTrTFJx_96WifgoHDgc-M7tI-SaQkaBlnebbGN7b6zHbehMxgBkBjwDECdkQqXgaUnV-ymZgCqKlDGqzslFCBsAKkCpCZktmsaamHRNsnKJ63ZJ6KsQXezjWAwR1zYJ0fcm9t6O3PpQ--7r0OIeB85ekrMG22CvfvKUvD0uVvPndPn69DKfLVOTFzSmRS1QccVQCqbQYC5KpWpeNlgzgWVBi6qmKGQFdZUzZoQUDQPJS8ylkKzkU3J7nLv33UdvQ9RbF4xtW9zZrg-a51SCEPkA3h9B47sQvG303rst-oOmoEdreqP_WtOjNQ1cD9aG5pufLRgMto3HnXHhdwKDnIMoxmsejpwdXv501utgnN0ZWzs_-NR15_6z7hstmInk</recordid><startdate>2008</startdate><enddate>2008</enddate><creator>Ergun, Celaletdin</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QQ</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>2008</creationdate><title>Effect of Ti ion substitution on the structure of hydroxylapatite</title><author>Ergun, Celaletdin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-5d7a9392a8729aca47699d36fad27a6515bd1a78b0db422c787f20836a4878263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Apatite</topic><topic>Applied sciences</topic><topic>Biological and medical sciences</topic><topic>Building materials. Ceramics. Glasses</topic><topic>CaTiO 3</topic><topic>Ceramic industries</topic><topic>Chemical industry and chemicals</topic><topic>Exact sciences and technology</topic><topic>Medical sciences</topic><topic>Miscellaneous</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>Sintering</topic><topic>Technical ceramics</topic><topic>Technology. Biomaterials. Equipments. Material. Instrumentation</topic><topic>Titanium substitution</topic><topic>Tri-calcium phosphate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ergun, Celaletdin</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Ceramic Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of the European Ceramic Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ergun, Celaletdin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Ti ion substitution on the structure of hydroxylapatite</atitle><jtitle>Journal of the European Ceramic Society</jtitle><date>2008</date><risdate>2008</risdate><volume>28</volume><issue>11</issue><spage>2137</spage><epage>2149</epage><pages>2137-2149</pages><issn>0955-2219</issn><eissn>1873-619X</eissn><abstract>In order to increase the understanding of the interaction of titanium (Ti) ions with hydroxylapatite (HA) structure, two different kinds of experiments were carried out. In the first, titanium ion containing HA was made via a precipitation method. Tetraethyl orthotitanate were added to precipitating HA to incorporate Ti ions into HA structure. The precipitates were dried and sintered in air at 500
°C, 700
°C, 900
°C, 1100
°C, and 1300
°C for 2
h. X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy analysis were used to characterize the samples. In the second, rather as the complementary experiments to the first set, powder mixtures of HA/CaTiO
3, tri-calcium phosphate/CaTiO
3 were sintered in air at 900
°C, 1100
°C, and 1300
°C for 2
h, and characterized with X-ray diffraction technique. Lattice parameters from X-ray diffraction spectra showed that Ti incorporation into the apatite structure caused lattice shrinkage. The grain sizes of substituted HAs were smaller than those of pure HA. Increasing the amount of the Ti ions in HA caused the decomposition of HA associated with the formation of α-tricalcium phosphate and CaTiO
3. This enhanced the porosity in titanium containing HA compared to pure HA. As also verified by the results of complementary experiments, α-tricalcium phosphate (TCP) and CaTiO
3 reacted at 1300
°C in the expense of both phases in the presence of HA. No reaction products in the form of new phases could be identified. On the other hand, the same reaction was not observed in the samples that did not have stable HA phase.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.jeurceramsoc.2008.03.007</doi><tpages>13</tpages></addata></record> |
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subjects | Apatite Applied sciences Biological and medical sciences Building materials. Ceramics. Glasses CaTiO 3 Ceramic industries Chemical industry and chemicals Exact sciences and technology Medical sciences Miscellaneous Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) Sintering Technical ceramics Technology. Biomaterials. Equipments. Material. Instrumentation Titanium substitution Tri-calcium phosphate |
title | Effect of Ti ion substitution on the structure of hydroxylapatite |
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