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AuthorZalnezhad, Erfan
AuthorMusharavati, F.
AuthorChen, Tianyi
AuthorJaber, Fadi
AuthorUzun, Kaan
AuthorChowdhury, Muhammad E. H.
AuthorKhandakar, Amith
AuthorLiu, Junxing
AuthorBae, S.
Available date2023-04-17T06:57:45Z
Publication Date2021
Publication NameScientific Reports
ResourceScopus
URIhttp://dx.doi.org/10.1038/s41598-021-81187-7
URIhttp://hdl.handle.net/10576/41976
AbstractIn this study, a combination of reverse microemulsion and hydrothermal techniques were used to synthesize HA. A hydrothermal method was used to synthesize HA/TiO2/CNT nanocomposite powders. Cold and hot isostatic pressing techniques were used to fabricate tablet-shaped samples. To investigate the biocompatibility and tribo-mechanical properties of HA/TiO2 and HA/TiO2/CNTs, four samples were prepared with different percentages of CNTs, namely, HA/TiO2 (S0), HA/TiO2/CNT (S1.0), HA/TiO2/CNT (S2.0), and HA/TiO2/CNT (S3.0). The microstructure and morphology of the HA/TiO2/CNTs were characterized by transmission electron microscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray diffraction. Hardness test results show that S3.0 displayed the highest surface hardness (285 HV) compared to other samples. The wear rate of HA/TiO2/CNT with the highest CNT content showed a decrease compared with those of the other samples. The results from nanoindentation tests showed that Young's modulus of the S3.0 sample was 58.1% greater than that of the S0 sample. Furthermore, the human MDA-MB-231 cell line demonstrated good binding to the surface of the samples in the in-vitro biocompatibility evaluation of the HA/TiO2/CNT composites. 2021, The Author(s).
SponsorThis work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (No. NRF-2020R1A4A1019074).
Languageen
PublisherNature Research
SubjectEngineering
Materials science
Medical research
TitleTribo-mechanical properties evaluation of HA/TiO2/CNT nanocomposite
TypeArticle
Issue Number1
Volume Number11
dc.accessType Open Access


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