Please use this identifier to cite or link to this item:
http://cmuir.cmu.ac.th/jspui/handle/6653943832/57335
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Apichart Han | en_US |
dc.contributor.author | Gobwute Rujijanagul | en_US |
dc.contributor.author | Chamnan Randorn | en_US |
dc.date.accessioned | 2018-09-05T03:38:45Z | - |
dc.date.available | 2018-09-05T03:38:45Z | - |
dc.date.issued | 2017-04-15 | en_US |
dc.identifier.issn | 18734979 | en_US |
dc.identifier.issn | 0167577X | en_US |
dc.identifier.other | 2-s2.0-85012266368 | en_US |
dc.identifier.other | 10.1016/j.matlet.2017.01.098 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85012266368&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/57335 | - |
dc.description.abstract | © 2017 Elsevier B.V. Here, a novel polyacrylamide (PAM)/hydroxyapatite (HA) composite hydrogel was prepared by the self-initiation of hydroxyapatite via its photocatalytic activity. The radical used as the initiator was produced during irradiation and can initiate the formation of the well-distributed HA in the PAM/HA composite. The in vitro bioactivity in SBF of the novel self-initiated PAM/HA(Ti) hydrogel was faster and better than the conventionally synthesized polyacrylamide hydrogel. The faster formation and larger amount of new apatite in SBF can be observed in the SEM images. | en_US |
dc.subject | Engineering | en_US |
dc.subject | Materials Science | en_US |
dc.subject | Physics and Astronomy | en_US |
dc.title | Preparation of hydroxyapatite hydrogel for bone-like materials via novel self-initiated photocatalytic polymerization | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Materials Letters | en_US |
article.volume | 193 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.