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    Electrochemical Properties of Ni 47 Ti 49 Co 4 Shape Memory Alloy in Artificial Urine for Urological Implant

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    Type
    Article
    Authors
    Ahmed, Rasha A.
    Date
    2015-08-20
    Online Publication Date
    2015-08-20
    Print Publication Date
    2015-09-02
    Permanent link to this record
    http://hdl.handle.net/10754/598138
    
    Metadata
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    Abstract
    © 2015 American Chemical Society. The corrosion performance of Ni47Ti49Co4 shape memory alloys (SMA) in artificial urine solution was evaluated in comparison with Ni51Ti49 alloy as reference, at 37°C and pH 5.6-6.4. SEM results revealed less pitting attack for Ni47Ti49Co4 SMA surface after immersion in artificial urine solution. The XRD analysis demonstrated the formation of passive film on Ni47Ti49Co4 SMA. The XPS analysis indicated that the film mainly consisted of O, Ti, Co, P, and a small amount of Ni, and the concentration of Ni ions release was greatly reduced compared to that of the Ni51Ti49 SMA. Linear polarization results illustrated that corrosion potential (Ecorr), corrosion current density (icorr), and ac polarization resistance (Rp) were affected greatly by alloying Co to Nitinol alloy. Our observations indicated that the corrosion resistance of the ternary alloy, Ni47Ti49Co4 SMA, offers superior corrosion resistance in artificial urine when compared to Ni51Ti49 SMA, which was suitable for medical applications.
    Citation
    Ahmed RA (2015) Electrochemical Properties of Ni 47 Ti 49 Co 4 Shape Memory Alloy in Artificial Urine for Urological Implant . Ind Eng Chem Res 54: 8397–8404. Available: http://dx.doi.org/10.1021/acs.iecr.5b00838.
    Sponsors
    I am grateful for the financial support of the Chemistry Department, University of Taif, Kingdom of Saudi Arabia. I also thank Core laboratories in King Abdullah University of Science and Technology (KAUST) for performing XRD and XPS analysis.
    Publisher
    American Chemical Society (ACS)
    Journal
    Industrial & Engineering Chemistry Research
    DOI
    10.1021/acs.iecr.5b00838
    ae974a485f413a2113503eed53cd6c53
    10.1021/acs.iecr.5b00838
    Scopus Count
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