Loading…

Electrochemical Properties of Hydroxyapatite Crystal Surfaces on Anatase Photocatalysts

Hydroxyapatite (HAp) was crystallized on anatase titanium dioxide (TiO2) photocatalytic crystals or their thin films using of a pseudo‐body solution method, and electrochemical properties of the HAp‐adhered anatase TiO2 photocatalytic surfaces were discussed. Decomposition rates of methylene blue we...

Full description

Saved in:
Bibliographic Details
Published in:Journal of the American Ceramic Society 2006-03, Vol.89 (3), p.944-948
Main Authors: Funakoshi, Kunio, Nonami, Toru
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c5712-6ecc8bf22c4cf3a4b0cfe94d2f2c4abc40451972a9c89f2395f66ff70e75d4a63
cites cdi_FETCH-LOGICAL-c5712-6ecc8bf22c4cf3a4b0cfe94d2f2c4abc40451972a9c89f2395f66ff70e75d4a63
container_end_page 948
container_issue 3
container_start_page 944
container_title Journal of the American Ceramic Society
container_volume 89
creator Funakoshi, Kunio
Nonami, Toru
description Hydroxyapatite (HAp) was crystallized on anatase titanium dioxide (TiO2) photocatalytic crystals or their thin films using of a pseudo‐body solution method, and electrochemical properties of the HAp‐adhered anatase TiO2 photocatalytic surfaces were discussed. Decomposition rates of methylene blue were faster for the HAp‐adhered anatase TiO2 photocatalysts, although specific surface areas were smaller than those for the commercial anatase TiO2 ones. Surface potential dispersions on the HAp‐adhered anatase TiO2 thin films before and after an ultraviolet light irradiation were measured by an atomic force microscopy. Changes in the color of leucocrystalviolet mixed in the HAp‐adhered anatase TiO2 photocatalysts or the commercial anatase TiO2 ones with experimental durations were compared. Movements of electrons from the anatase TiO2 photocatalytic surfaces to the HAp, crystals and oxidizing reactions on the HAp‐adhered anatase TiO2 photocatalytic surfaces in the dark were discussed on the basis of these experimental results.
doi_str_mv 10.1111/j.1551-2916.2005.00802.x
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_28021740</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1044570041</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5712-6ecc8bf22c4cf3a4b0cfe94d2f2c4abc40451972a9c89f2395f66ff70e75d4a63</originalsourceid><addsrcrecordid>eNqNkV1r2zAUhkXZYFm3_2AGK7uxJ8n6vCqZSdON0qaso70TiiJRZ46VSgqN__3kpnSwi1Hd6Os5j9B5ASgQrFAeX9cVohSVWCJWYQhpBaGAuNofgcnLxRswgRDikgsM34H3Ma7zFklBJuB21lmTgjf3dtMa3RWL4Lc2pNbGwrvifFgFvx_0Vqc22aIJQ0wZ-rkLTpsR6Ytpr5OOtljc--RNXneZiR_AW6e7aD8-z8fg19nspjkvL67m35vpRWkoR7hk1hixdBgbYlytyRIaZyVZYZdP9NIQSCiSHGtphHS4ltQx5hyHltMV0aw-BicH7zb4h52NSW3aaGzX6d76XVQ4NwNxAl8DoloKlMEv_wURFBgJxsmIfvoHXftd6PN_VX5UorHFGRIHyAQfY7BObUO70WHIJjVGqNZqTEqNSakxQvUUodrn0s_Pfh1zNi7o3rTxbz1nmBHKM3d64B7bzg6v9qsf02b2tM6G8mBoY7L7F4MOvxXjNafq9nKuLptvd4vrG6Tm9R_aNL61</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>217911984</pqid></control><display><type>article</type><title>Electrochemical Properties of Hydroxyapatite Crystal Surfaces on Anatase Photocatalysts</title><source>Wiley</source><creator>Funakoshi, Kunio ; Nonami, Toru</creator><creatorcontrib>Funakoshi, Kunio ; Nonami, Toru</creatorcontrib><description>Hydroxyapatite (HAp) was crystallized on anatase titanium dioxide (TiO2) photocatalytic crystals or their thin films using of a pseudo‐body solution method, and electrochemical properties of the HAp‐adhered anatase TiO2 photocatalytic surfaces were discussed. Decomposition rates of methylene blue were faster for the HAp‐adhered anatase TiO2 photocatalysts, although specific surface areas were smaller than those for the commercial anatase TiO2 ones. Surface potential dispersions on the HAp‐adhered anatase TiO2 thin films before and after an ultraviolet light irradiation were measured by an atomic force microscopy. Changes in the color of leucocrystalviolet mixed in the HAp‐adhered anatase TiO2 photocatalysts or the commercial anatase TiO2 ones with experimental durations were compared. Movements of electrons from the anatase TiO2 photocatalytic surfaces to the HAp, crystals and oxidizing reactions on the HAp‐adhered anatase TiO2 photocatalytic surfaces in the dark were discussed on the basis of these experimental results.</description><identifier>ISSN: 0002-7820</identifier><identifier>EISSN: 1551-2916</identifier><identifier>DOI: 10.1111/j.1551-2916.2005.00802.x</identifier><identifier>CODEN: JACTAW</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>Anatase ; Chemistry ; Crystal surfaces ; Crystals ; Electric properties ; Exact sciences and technology ; General and physical chemistry ; Hydroxyapatite ; Photocatalysis ; Photocatalysts ; Photochemistry ; Physical chemistry of induced reactions (with radiations, particles and ultrasonics) ; Specific surface ; Thin films ; Titanium dioxide</subject><ispartof>Journal of the American Ceramic Society, 2006-03, Vol.89 (3), p.944-948</ispartof><rights>2007 INIST-CNRS</rights><rights>Copyright American Ceramic Society Mar 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5712-6ecc8bf22c4cf3a4b0cfe94d2f2c4abc40451972a9c89f2395f66ff70e75d4a63</citedby><cites>FETCH-LOGICAL-c5712-6ecc8bf22c4cf3a4b0cfe94d2f2c4abc40451972a9c89f2395f66ff70e75d4a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17626457$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Funakoshi, Kunio</creatorcontrib><creatorcontrib>Nonami, Toru</creatorcontrib><title>Electrochemical Properties of Hydroxyapatite Crystal Surfaces on Anatase Photocatalysts</title><title>Journal of the American Ceramic Society</title><description>Hydroxyapatite (HAp) was crystallized on anatase titanium dioxide (TiO2) photocatalytic crystals or their thin films using of a pseudo‐body solution method, and electrochemical properties of the HAp‐adhered anatase TiO2 photocatalytic surfaces were discussed. Decomposition rates of methylene blue were faster for the HAp‐adhered anatase TiO2 photocatalysts, although specific surface areas were smaller than those for the commercial anatase TiO2 ones. Surface potential dispersions on the HAp‐adhered anatase TiO2 thin films before and after an ultraviolet light irradiation were measured by an atomic force microscopy. Changes in the color of leucocrystalviolet mixed in the HAp‐adhered anatase TiO2 photocatalysts or the commercial anatase TiO2 ones with experimental durations were compared. Movements of electrons from the anatase TiO2 photocatalytic surfaces to the HAp, crystals and oxidizing reactions on the HAp‐adhered anatase TiO2 photocatalytic surfaces in the dark were discussed on the basis of these experimental results.</description><subject>Anatase</subject><subject>Chemistry</subject><subject>Crystal surfaces</subject><subject>Crystals</subject><subject>Electric properties</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Hydroxyapatite</subject><subject>Photocatalysis</subject><subject>Photocatalysts</subject><subject>Photochemistry</subject><subject>Physical chemistry of induced reactions (with radiations, particles and ultrasonics)</subject><subject>Specific surface</subject><subject>Thin films</subject><subject>Titanium dioxide</subject><issn>0002-7820</issn><issn>1551-2916</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqNkV1r2zAUhkXZYFm3_2AGK7uxJ8n6vCqZSdON0qaso70TiiJRZ46VSgqN__3kpnSwi1Hd6Os5j9B5ASgQrFAeX9cVohSVWCJWYQhpBaGAuNofgcnLxRswgRDikgsM34H3Ma7zFklBJuB21lmTgjf3dtMa3RWL4Lc2pNbGwrvifFgFvx_0Vqc22aIJQ0wZ-rkLTpsR6Ytpr5OOtljc--RNXneZiR_AW6e7aD8-z8fg19nspjkvL67m35vpRWkoR7hk1hixdBgbYlytyRIaZyVZYZdP9NIQSCiSHGtphHS4ltQx5hyHltMV0aw-BicH7zb4h52NSW3aaGzX6d76XVQ4NwNxAl8DoloKlMEv_wURFBgJxsmIfvoHXftd6PN_VX5UorHFGRIHyAQfY7BObUO70WHIJjVGqNZqTEqNSakxQvUUodrn0s_Pfh1zNi7o3rTxbz1nmBHKM3d64B7bzg6v9qsf02b2tM6G8mBoY7L7F4MOvxXjNafq9nKuLptvd4vrG6Tm9R_aNL61</recordid><startdate>200603</startdate><enddate>200603</enddate><creator>Funakoshi, Kunio</creator><creator>Nonami, Toru</creator><general>Blackwell Publishing Inc</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QQ</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>200603</creationdate><title>Electrochemical Properties of Hydroxyapatite Crystal Surfaces on Anatase Photocatalysts</title><author>Funakoshi, Kunio ; Nonami, Toru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5712-6ecc8bf22c4cf3a4b0cfe94d2f2c4abc40451972a9c89f2395f66ff70e75d4a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Anatase</topic><topic>Chemistry</topic><topic>Crystal surfaces</topic><topic>Crystals</topic><topic>Electric properties</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Hydroxyapatite</topic><topic>Photocatalysis</topic><topic>Photocatalysts</topic><topic>Photochemistry</topic><topic>Physical chemistry of induced reactions (with radiations, particles and ultrasonics)</topic><topic>Specific surface</topic><topic>Thin films</topic><topic>Titanium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Funakoshi, Kunio</creatorcontrib><creatorcontrib>Nonami, Toru</creatorcontrib><collection>Istex</collection><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 American Ceramic Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Funakoshi, Kunio</au><au>Nonami, Toru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemical Properties of Hydroxyapatite Crystal Surfaces on Anatase Photocatalysts</atitle><jtitle>Journal of the American Ceramic Society</jtitle><date>2006-03</date><risdate>2006</risdate><volume>89</volume><issue>3</issue><spage>944</spage><epage>948</epage><pages>944-948</pages><issn>0002-7820</issn><eissn>1551-2916</eissn><coden>JACTAW</coden><abstract>Hydroxyapatite (HAp) was crystallized on anatase titanium dioxide (TiO2) photocatalytic crystals or their thin films using of a pseudo‐body solution method, and electrochemical properties of the HAp‐adhered anatase TiO2 photocatalytic surfaces were discussed. Decomposition rates of methylene blue were faster for the HAp‐adhered anatase TiO2 photocatalysts, although specific surface areas were smaller than those for the commercial anatase TiO2 ones. Surface potential dispersions on the HAp‐adhered anatase TiO2 thin films before and after an ultraviolet light irradiation were measured by an atomic force microscopy. Changes in the color of leucocrystalviolet mixed in the HAp‐adhered anatase TiO2 photocatalysts or the commercial anatase TiO2 ones with experimental durations were compared. Movements of electrons from the anatase TiO2 photocatalytic surfaces to the HAp, crystals and oxidizing reactions on the HAp‐adhered anatase TiO2 photocatalytic surfaces in the dark were discussed on the basis of these experimental results.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><doi>10.1111/j.1551-2916.2005.00802.x</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0002-7820
ispartof Journal of the American Ceramic Society, 2006-03, Vol.89 (3), p.944-948
issn 0002-7820
1551-2916
language eng
recordid cdi_proquest_miscellaneous_28021740
source Wiley
subjects Anatase
Chemistry
Crystal surfaces
Crystals
Electric properties
Exact sciences and technology
General and physical chemistry
Hydroxyapatite
Photocatalysis
Photocatalysts
Photochemistry
Physical chemistry of induced reactions (with radiations, particles and ultrasonics)
Specific surface
Thin films
Titanium dioxide
title Electrochemical Properties of Hydroxyapatite Crystal Surfaces on Anatase Photocatalysts
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T15%3A02%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Electrochemical%20Properties%20of%20Hydroxyapatite%20Crystal%20Surfaces%20on%20Anatase%20Photocatalysts&rft.jtitle=Journal%20of%20the%20American%20Ceramic%20Society&rft.au=Funakoshi,%20Kunio&rft.date=2006-03&rft.volume=89&rft.issue=3&rft.spage=944&rft.epage=948&rft.pages=944-948&rft.issn=0002-7820&rft.eissn=1551-2916&rft.coden=JACTAW&rft_id=info:doi/10.1111/j.1551-2916.2005.00802.x&rft_dat=%3Cproquest_cross%3E1044570041%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c5712-6ecc8bf22c4cf3a4b0cfe94d2f2c4abc40451972a9c89f2395f66ff70e75d4a63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=217911984&rft_id=info:pmid/&rfr_iscdi=true