USING OF CoCr ALLOYS IN BIOMEDICAL APPLICATIONS ( REVIEW)

Metals are used extensively in biomedical applications due to their mechanical strength, corrosion resistance, and biocompatibility. There are many types of metals and alloys used in this application ( stainless steel, Ti and Ti alloys, CoCr, dental amalgam, etc). This review focus on CoCr alloys which have excellent corrosion resistance and mechanical properties which make them the best choice for many types of surgical implants. There are many alloying elements used to improve the properties of CoCr alloy such as ( Zr, In, Ta, etc ) has been reviewed.

Synthesis and Characterization of Ti-Sn Alloy for Orthopedic Application

Titanium (Ti)-based alloys (e.g., Ti6Al4V) are widely used in orthopedic implant applications owing to their excellent mechanical properties and biocompatibility. However, their corrosion resistance needs to be optimized. In addition, the presence of aluminum and vanadium cause alzheimer and cancer, respectively. Therefore, in this study, titanium-based alloys were developed via powder metallurgy route. In these alloys, the Al and V were replaced with tin (Sn) which was the main aim of this study. Four sets of samples were prepared by varying Sn contents, i.e., 5 to 20 wt. %. This was followed by characterization techniques including laser particle analyzer (LPA), X-ray diffractometer (XRD), scanning electron microscope (SEM), computerized potentiostate, vicker hardness tester, and nanoindenter. Results demonstrate the powder sizes between 50 and 55 µm exhibiting very good densification after sintering. The alloy contained alpha at all concentrations of Sn. However, as Sn content in the alloy exceeded from 10 wt. %, the formation of intermetallic compounds was significant. Thus, the presence of such intermetallic phases are attributed to enhanced elastic modulus. In particular, when Sn content was between 15 and 20 wt. % a drastic increase in elastic modulus was observed thereby surpassing the standard/reference alloy (Ti6Al4V). However, at 10 wt. % of Sn, the elastic modulus is more or less comparable to reference counterpart. Similarly, hardness was also increased in an ascending order upon Sn addition, i.e., 250 to 310 HV. Specifically, at 10 wt. % Sn, the hardness was observed to be 250 HV which is quite near to reference alloy, i.e., 210 HV. Moreover, tensile strength (TS) of the alloys were calculated using hardness values since it was very difficult to prepare the test coupons using powders. The TS values were in the range of 975 to 1524 MPa at all concentrations of Sn. In particular, the TS at 10 wt. % Sn is 1149 MPa which is comparable to reference counterpart (1168 MPa). The corrosion rate of Titanium-Sn alloys (as of this study) and reference alloy, i.e., Ti6Al4V were also compared. Incorporation of Sn reduced the corrosion rate at large than that of reference counterpart. In particular, the trend was in decreasing order as Sn content increased from 5 to 20 wt. %. The minimum corrosion rate of 3.65 × 10−9 mm/year was noticed at 20 wt. % than that of 0.03 mm/year of reference alloy. This shows the excellent corrosion resistance upon addition of Sn at all concentrations.

Pulsed plasma nitriding of high velocity oxy-fuel sprayed Inconel 625 coatings

A hardening of high velocity oxy-fuel sprayed Inconel 625 coating systems was performed by pulsed plasma nitriding treatment. After deposition of an Inconel 625 coating, samples were pulsed plasma nitrided at 520 °C for 12 h in a gas ratio of 3:1 N2 and H2 under a constant pressure of 2.5 × 102 Pa. Pulsed plasma nitriding improved the microhardness of the high velocity oxy-fuel sprayed Inconel 625 coating from 355 to 401 HV0.05. The high velocity oxy-fuel-sprayed Inconel 625 coating after pulsed plasma nitriding process showed excellent corrosion resistance as well as a reduction of both the friction coefficient and wear rate during the sliding phase in a 3.5 wt.% NaCl solution against sliding action of Al2O3 ball.

Defining-Measuring-Analysing-Improving-Controlling (DMAIC): Process and Improve Stability in Carbon Steel Industry

Phosphating is most common method for surface treatment and finishing of ferrous and nonferrous metal. It has excellent corrosion resistance, wear resistance, adhesion and lubricating properties besides its economic values and speed of application. Steel is one of the cheapest materials used in various industries and it requires corrosion resistance therapy. This study aims to provide possible solution to the rusty issue on carbon steel product by improving coating stability using Defining–Measuring–Analysing–Improving–Controlling (DMAIC) method. The result proposed that zinc phosphate coating material has to replace current iron phosphate coating due to the former is more corrosion time resistant than that of the latter.

High-Temperature Chemical Stability of Cr(III) Oxide Refractories in the Presence of Calcium Aluminate Cement

Al2O3-CaO-Cr2O3 castables are used in various furnaces due to excellent corrosion resistance and sufficient early strength, but toxic Cr(VI) generation during service remains a concern. Here, we investigated the relative reactivity of analogous Cr(III) phases such as Cr2O3, (Al1-xCrx)2O3 and in situ Cr(III) solid solution with the calcium aluminate cement under an oxidizing atmosphere at various temperatures. The aim is to comprehend the relative Cr(VI) generation in the low-cement castables (Al2O3-CaO-Cr2O3-O2 system) and achieve an environment-friendly application. The solid-state reactions and Cr(VI) formation were investigated using powder XRD, SEM, and leaching tests. Compared to Cr2O3, the stability of (Al1-xCrx)2O3 against CAC was much higher, which improved gradually with the concentration of Al2O3 in (Al1-xCrx)2O3. The substitution of Cr2O3 with (Al1-xCrx)2O3 in the Al2O3-CaO-Cr2O3 castables could completely inhibit the formation of Cr(VI) compound CaCrO4 at 500–1100 °C and could drastically suppress Ca4Al6CrO16 generation at 900 to 1300 °C. The Cr(VI) reduction amounting up to 98.1% could be achieved by replacing Cr2O3 with (Al1-xCrx)2O3 solid solution. However, in situ stabilized Cr(III) phases as a mixture of (Al1-xCrx)2O3 and Ca(Al12-xCrx)O19 solid solution hardly reveal any reoxidation. Moreover, the CA6 was much more stable than CA and CA2, and it did not participate in any chemical reaction with (Al1-xCrx)2O3 solid solution.