Corrosion behaviour in physiological fluids of surface films formed on titanium alloys

The properties of the surface films formed on Ti and its Ti–5Al–4V and Ti–6Al–3.5Fe alloys by chemical (immersion in 10 M NaOH) and thermal treatment (500 °C) were studied in this paper. Their corrosion behaviour in Ringer solution was investigated. After treatments, the sample microhardness was measured. Also, the sample surfaces were observed by an optical microscope before and after immersion in Ringer solutions. The electrochemical behaviour of the surface films obtained by the chemical and thermal treatments was studied using the methods of the electrochemical impedance spectroscopy (EIS) and monitoring of open circuit potentials at different immersion periods (up to 60 days) in Ringer solution. Microhardness increased with the increasing loads for the studied materials, showing the existence of a compact protective layer. Microscopic observations exhibited more compact coatings after 60 days of exposure in Ringer solution, due to the formation of an apatite layer. EIS spectra revealed surface films with two layers: an inner, barrier protective layer and an outer, porous apatite layer. The impedance increases in time denoting that the films have grown by apatite nucleation. Also, EIS spectra showed that the complex treatment by chemical + heat method is the most efficiently. For the samples treated by the two processes (chemical + heat) the values of the open circuit potentials are nobler than of the chemical treated samples, denoting better protective, bioactive films.     

Use of FIB to Study ZDDP Tribofilms

Focussed ion beam milling (FIB) followed by TEM has been used to study ZDDP tribofilms on rubbed steel surfaces. It has been found that the impact of high energy platinum and gallium ions during FIB causes significant morphological and structural changes to the uppermost 30–50 nm of a ZDDP tribofilm. This can be prevented by the low energy deposition of a quite thick gold layer prior to installation of the sample in the FIB facility. This problem, and its solution, have been quite widely reported in the non-tribology literature but have not previously been highlighted in the application of FIB to study tribological surfaces. It has also been found, using this gold pre-deposition method, that the bulk of the ZDDP tribofilm studied has a polycrystalline structure.     

Sorption/release of diclofenac sodium in/from free‐standing poly(acrylic acid)/poly(ethyleneimine) multilayer films

Polyelectrolyte multilayer films deposited onto various substrates have been used extensively as drug delivery systems. However, little attention has been paid to the release of drugs from free‐standing polymeric films. Herein, we report the construction of thermal crosslinked free‐standing poly(acrylic acid) (PAA)/branched poly(ethyleneimine) (PEI) multilayer films composed of 25 double layers [(PAA/PEI)₂₅] and their use in sorption/release of diclofenac sodium (DS). The (PAA/PEI)₂₅ multilayer films were characterized by scanning electron microscopy, potentiometric titrations and Fourier transform infrared spectroscopy, while the sorption/release of DS was monitored by UV – Vis spectroscopy. The DS sorption equilibrium data were fitted with five isotherm models (Langmuir, Freundlich, Sips, Dubinin–Radushkevich, and Temkin). The maximum equilibrium sorption capacity, q_m, given by the Langmuir model was 32.42 mg DS/g. The Korsmeyer–Peppas semiempirical equation showed that the release of DS from the free‐standing (PAA/PEI)₂₅ films proceeded by pseudo‐Fickian diffusion, irrespective of the releasing media. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43752.     

Specific interactions in ternary system quaternized polysulfone/mixed solvent

Theoretical and experimental aspects on the specific interactions developed via electrostatic interactions and hydrogen‐bonding in a ternary system formed of a proton‐donor solvent (N,N‐dimethylformamide or methanol), a proton‐acceptor solvent (water), and a quaternized polysulfone with various contents of ionic chlorine, which indicates a proton‐acceptor character, are investigated. Thus, the interactions of the ternary systems are corrected on the basis of the association phenomena defined through association constants. Numerical values for these constants were evaluated as a function of the system composition, by mathematical simulations for an accurate adjustment of preferential adsorption, determined by the Flory–Huggins–Pouchly theoretical approach applied to the experimental data. POLYM. ENG. SCI., 2009. © 2008 Society of Plastics Engineers     

Surface and interface properties of functionalized polysulfones: Cell‐material interaction and antimicrobial activity

Quaternized polysulfones with different ionic chlorine content tested for biomedical applications were obtained by quaternization reaction of chloromethylated polysulfones with N,N‐dimethylethanolamine. The relationship between the different physical and chemical characteristics of these polymers and their biocompatible and antimicrobial properties was established for maximizing the selectivity and performance of these materials for biomedical applications. Therefore, topographic reorganization of the polysulfonic films induced by the type of nonsolvent in casting solutions of polymer significantly influences films morphology, depending on the charge density of polyelectrolytes, the hydrophilic/hydrophobic characteristics, as well as on the history of the formed films. Furthermore, the study of the adhesion of red blood cells and cohesion of platelets on the surface of quaternized polysulfone films, as well as analysis of antibacterial activity, using Pseudomonas aeruginosa ATCC 27853 and Staphylococcus aureus ATCC 25923 microorganisms, contribute to extending the possible applications of quaternized polysulfones as semipermeable membranes in biomedical domains. POLYM. ENG. SCI., 55:2184–2194, 2015. © 2015 Society of Plastics Engineers     

Impact of Some Properties of Quaternized Polysulfone/Poly(Vinylidene Fluoride) Blend on the Potential Biomedical Applications

Blends of quaternized polysulfones with triphenylphosphonium pendant groups/poly(vinylidene fluoride) were analyzed to establish their impact on the rheological, morphological and surface properties, as well as their interactions with some blood compounds. The rheological functions reflect the influence of both polymers’ chemical structures. Blend compositions of the corresponding films influence the surface tension parameters, increase blend hydrophobicity and, implicitly, decrease the polar surface tension parameters. The specific surface characteristics of polymer blends are related to their interactions with some blood constituents and plasma proteins. Also, the specific microarchitecture of the blend represents an excellent scaffold for medical applications.     

Microstructure,mechanical properties,and corrosion resistance of Ti-20Zr alloy in undoped and NaF doped artificial saliva

The corrosion behavior of a new, advanced Ti-20Zr alloy with α+β microstructure (determined by optical microscopy, XRD, and SEM) and very good mechanical properties (obtained from the stress-strain curve) is studied in this paper. The composition of the alloy native passive film was determined from a XPS analysis and the long-term corrosion resistance in undoped and doped states with 0.05M NaF artificial Carter-Brugirard saliva of different pH values, simulating the severe functional conditions of a dental implant, was analyzed by electrochemical methods. This alloy possesses an advantageous balance between good mechanical resistance and plasticity and Young’s modulus and exhibits more favorable electrochemical parameters and corrosion resistance than CP Ti due to its more resistant passive layer containing Ti₂O₃, TiO₂, and ZrO₂ protective oxides. After 1000 h of immersion in saliva, the protective properties of the alloy were enhanced due to the deposited surface layer that incorporated protective phosphates (shown by SEM and XPS).     

Synthesis and characterization of collagen/hydroxyapatite: magnetite composite material for bone cancer treatment

Our purpose was obtaining and characterizing a complex composite system with multifunctional role: bone graft material and hyperthermia generator necessary for bone cancer therapy. The designed system was a magnetite enriched collagen/hydroxyapatite composite material, obtained by a co-precipitation method. Due to the applied electromagnetic field the magnetite will induce hyperthermia and cause tumoral cell apoptosis. The complex bone graft system was characterised by XRD, FTIR and SEM, while the hyperthermia was quantify by measuring the temperature increase due to the applied alternative electromagnetical field.     

In vitro assessment and monitoring of the implant titanium materials – physiological environment interactions

Long‐term monitoring (for 8000 exposure hours) of titanium and its implant alloys (Ti‐5Al‐4V, Ti‐6Al‐4Fe) interactions with Ringer's solutions of different pH‐values (2.5, 4.35, 6.98), simulating various conditions that can appear at the contact between implant and tissues was carried out in this paper. All data were statistics treated using Medcalc program. In vitro electrochemical behaviour of titanium and its alloys reveals their self‐passivation in Ringer's solutions. Monitoring of the open circuit potentials with time and pH have shown that the passive films on the implant materials studied were very stable for all tested periods. Interactions due to the non‐uniformity of the physiological electrolyte pH can not produce any form of local corrosion. The tested materials present low corrosion rates which attest their very good stability for 8000 exposure hours in simulated biological environment. Surface topography characterisation using atomic force microscopy (AFM) data, correlated with the electrochemical parameters, were arguments for the stability of the samples in studied bioliquids.     

Adsorption characteristics of UO(2)(2+) and Th(4+) ions from simulated radioactive solutions onto chitosan/clinoptilolite sorbents

Adsorption features of UO(2)(2+) and Th(4+) ions from simulated radioactive solutions onto a novel chitosan/clinoptilolite (CS/CPL) composite as beads have been investigated compared with chitosan cross-linked with epichlorohydrin. The effects of contact time, the initial metal ion concentration, sorbent mass and temperature on the adsorption capacity of the CS-based sorbents were investigated. The adsorption kinetics was well described by the pseudo-second order equation, and the adsorption isotherms were better fitted by the Sips model. The maximum experimental adsorption capacities were 328.32 mg Th(4+)/g composite, and 408.62 mg UO(2)(2+)/g composite. The overall adsorption tendency of CS/CPL composite toward UO(2)(2+) and Th(4+) radiocations in the presence of Cu(2+), Fe(2+) and Al(3+), under competitive conditions, followed the order: Cu(2+)>UO(2)(2+)>Fe(2+)>Al(3+), and Cu(2+)>Th(4+)>Fe(2+)>Al(3+), respectively. The negative values of Gibbs free energy of adsorption indicated the spontaneity of the adsorption of radioactive ions on both the CS/CPL composite and the cross-linked CS. The desorption level of UO(2)(2+) from the composite CS/CPL, by using 0.1M Na(2)CO(3), was around 92%, and that of Th(4+) ions, performed by 0.1M HCl, was around 85%, both values being higher than the desorption level of radiocations from the cross-linked CS, which were 89% and 83%, respectively.