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The consequence of coupling wear (erosion/abrasion) and corrosion is not just simply the sum of wear in the absence of corrosive medium and corrosion in absence of wear. The so-called synergistic effect implies that corrosion is accelerated due to the removal of the passivating layer because of wear. On the other hand, corrosion can accelerate abrasion when the electrochemical dissolution yields a brittle surface layer which can be subsequently removed by abrasion. The synergism between wear and corrosion is complex and the interaction between mechanical and chemical factors governing tribocorrosion is not yet fully understood. This review aims at providing a general and thorough summary of the wear-corrosion interaction focused on stainless steels due to the technological relevance of these materials. It is taken into consideration the influence of the key parameters affecting wear-corrosion, such as the stainless steel type, slurry characteristics (temperature, pH, solid concentration), the erodent properties (particle size and shape), etc. The different models to describe wear-corrosion and the most used apparatus for tribocorrosion testing are also reviewed.

A novel radiation grafted ETFE based proton conducting membrane was prepared by double irradiation grafting of two different monomers. The intrinsic oxidative stability of the ETFE-g-poly(styrene sulfonic acid-co-divinylbenzene) membrane was improved by reducing the gas crossover through incorporation of polymethacrylonitrile (PMAN) containing the strong polar nitrile group. A fuel cell test was carried out at 80 °C under constant current density of 500 mA cm−2 for a time exceeding 1′900 h. The incorporation of PMAN considerably improves the interfacial properties of the membrane-electrode assembly. No significant change in the membrane hydrogen crossover and performance over the testing time was observed, except for a measured decrease in the membrane ohmic resistance after 1′000 h. The combination of the double irradiation induced grafting with the use of the PMAN as gas barrier in addition to its chelating abilities (e. g. Ce3+) offers a promising strategy to develop more durable membranes for fuel cells.

International audience; This work aims to develop an injectable and antibacterial composite cement for bone substitution and prevention/treatment of bone infections. This cement is composed of calcium phosphate, calcium carbonate, bioactive glass, sodium alginate, and ciprofloxacin. The effect of ciprofloxacin on the microstructure, chemical composition, setting properties, cohesion, injectability, and compressive strength was investigated. The in vitro drug release kinetics and the antibacterial activity of ciprofloxacin-loaded composites against staphylococcus aureus and Escherichia coli pathogens were investigated. XRD and FTIR analysis demonstrated that the formulated cements are composed of a nanocrystalline carbonated apatite analogous to the mineral part of the bone. The evaluation of the composite cement’s properties revealed that the incorporation of 3 and 9 wt% of ciprofloxacin affects the microstructural and physicochemical properties of the cement, resulting in a prolonged setting time, and a slight decrease in injectability and compressive strength. The in vitro drug release study revealed sustained release profiles over 18 days. The amounts of ciprofloxacin released per day (0.2 -15.2 mg/L) depend on the cement composition and the amount of ciprofloxacin incorporated. The antibacterial activity of ciprofloxacin-loaded cement composites attested to their effectiveness to inhibit the growth of Staphylococcus aureus and Escherichia coli.

This work investigates the isolation of cellulose nanocrystals (CNC) from sugarcane bagasse (SCB) waste and the evaluation of their mechanical reinforcement capability for k-carrageenan biopolymer. The results from Atomic Force Microscopy and Transmission Electron Microscopy indicated the successful extraction of CNC from SCB following alkali, bleaching and acid hydrolysis treatments. The CNC displayed a needle-like structure with an average aspect ratio of 55. The surface functionality of the CNC was evaluated by Fourier Transform Infrared Spectroscopy and X-ray Photoelectron Spectroscopy measurements. X-ray diffraction studies showed that the as-extracted CNC exhibit cellulose I crystalline structure, with a crystallinity index of 80%. The obtained CNC were dispersed into k-carrageenan biopolymer matrix at various CNC contents (1, 3, 5 and 8 wt%) and the prepared films were further characterized. The incorporation of CNC decreased the light transmittance values but enhanced the mechanical properties compared with the neat k-carrageenan film. Empirical Halpin-Tsai model was used to predict the CNC dispersion within k-carrageenan matrix. The obtained nanocomposite films have the potential to be used as food packaging material.

In the present work, cellulose nanocrystals (CNC) were produced from vine shoots waste using chemical treatments followed by acid hydrolysis process. FTIR analysis confirmed that the non-cellulosic components were progressively removed during the chemical treatments, and the final obtained materials are composed of pure cellulose. AFM and TEM observations showed that the extracted CNC possess a needle-like shape with an average length of 456 nm and an average diameter of 14 nm, giving rise to an average aspect ratio of about 32. The as-extracted CNC exhibit a cellulose I structure with high crystallinity index (82%), as determined by XRD characterization. Importantly, the resulted CNC provide a higher thermal stability in comparison with CNC extracted from other resources, using the same extraction process. The isolated CNC's surface charge density was evaluated by XPS analysis and resulted in ~2.0 sulfate groups per 100 anhydroglucose units. In order to identify the reinforcing ability of the new extracted CNC, Carboxymethyl cellulose nanocomposite films were prepared with various CNC contents (1, 3, 5, 8 wt%) and their mechanical properties were investigated by uniaxial tensile test. The results showed that the as-extracted CNC displayed a higher reinforcing ability for nanocomposite materials.

Inverse vulcanization copolymers (p(S-DVB)) from the radical polymerization of elemental sulfur and divinylbenzene (DVB) have been studied as cathode active materials in poly(ethylene oxide) (PEO)-based all-solid-state Li-S cells. The Li-S cell comprising the optimized p(S-DVB) cathode (80:20 w/w S/DVB ratio) and lithium bis(fluorosulfonyl)imide/PEO (LiFSI/PEO) electrolyte shows high specific capacity (ca. 800 mAh g −1 ) and high Coulombic efficiency for 50 cycles. Most importantly, polysulfide (PS) shuttle is highly mitigated due to the strong interactions of PS species with polymer backbone in p(S-DVB). This is demonstrated by the stable cycling of the p(S-DVB)-based cell using lithium bis(trifluoromethanesulfonyl)imide (LiTFSI)/PEO electrolyte, where successful charging cannot be achieved even at the first cycle with plain elemental S-based cathode material due to the severe PS shuttle phenomenon. These results suggest that inverse vulcanization copolymers are promising alternatives to elemental sulfur for enhancing the electrochemical performance of PEO-based all-solid-state Li-S cells.

Carboxymethyl chitin (CMChit) has the potential to be used as a solid polymer electrolyte (SPE) based on its ionic conductivity value of the order of 10−6 S·cm−1 in self-standing membranes. In controlled humidity of 65RH%, carboxymethyl chitin based membrane blended with 1-Butyl-3-methylimidazolium acetate (BMIM[Ac]) ionic liquid (IL) (40 wt%) showed a threshold value of ionic conductivity in the order of 10−4 S·cm−1 and electrochemical stability was up to 2.93 V. The effects of the relative humidity and ionic liquid weight fraction on the ionic conductivity and structural changes were investigated in detail. Furthermore, the X-ray diffraction (XRD) diffractogram indicated a clear reduction of crystallinity of the CMChit. The Field-emission scanning electron microscopy (FESEM) observation of the cross-sections confirmed the homogeneity of the prepared blend. This electrolyte was tested in symmetric cells based on Zn//SPE//Zn and showed good reversibility and potential for application in proton-conducting batteries.

A correlation between the crystal structure, the ionic conductivity and the electrochemical performance in Lithium-ion batteries was established for a series of NASICON-type phosphates Li0.5M0.5Ti1.5Fe0.5(PO4)3 (M = Mn, Co, Mg). These electrode materials, where the M1 site contains both lithium and the divalent cation M, were prepared using a simple sol-gel process while controlling the pH and the final synthesis temperature. The three phosphates crystallize in the rhombohedral system (S.G. R-3c) with comparable unit cell parameters but with slight difference in the local distortion of the PO4 tetrahedra as confirmed by the Raman study. The ionic conductivities of the Li0.5M0.5Ti1.5Fe0.5(PO4)3 materials were measured at different temperatures using a wide range of frequencies. Mn-based phosphate shows the best features for application as electrode material for Li-ion batteries in term of the conductivity at room temperature and the activation energy of Li+ conduction process. The initial discharge capacity of 100 mAh.g − 1 was obtained for the Mg-based phosphate, 104.3 mAh.g − 1 for the Co-based material while the Mn-based material delivers the best first discharge capacity of 125.3 mAh.g − 1 with the lowest polarization in relation with its better conduction properties. This result was also confirmed by the rate capability tests where Mn-based phosphate shows enhanced electrochemical performance even at fast rate of 5C.

New synthesis route of polysalt with single ion conductivity based on functionalization of polyacrylic acid is reported for all solid state lithium metal batteries. Poly[(trifluoromethyl)sulfonyl acrylamide] PA–LiTFSI was synthesized in two steps reaction. The degree of functionalization of the polymer backbone by anion of lithium salt bis(trifluoromethane)sulfonimide (LiTFSI) was confirmed by ICP analysis. An ionic conductivity equal 1,77 10 −5 S cm −1 at 80 °C of polysalt blended with PEO is reported. Easy process-able polysalt blended with PEO exhibits good mechanical properties and high transference number.

Semi-interpenetrated network Solid Polymer Electrolytes (SPEs) were fabricated by UV-induced cross-linking of poly(ethyleneglycol) diacrylate (PEGDA) and divinylbenzene (DVB) within a poly(ethyleneoxide) (PEO) matrix (Mv = 5 × 106 g mol−1), comprising lithium bis(trifluoromethanesulfonyl)imide salt (LiTFSI), at a molar ratio of EO:Li ∼ 30:1. The influence of the DVB content on the final SPE properties was investigated in detail. An increase of DVB concentration resulted in self-standing polymer electrolytes. The DVB cross-linker incorporation was found to decrease the crystallinity of the PEO matrix from 34% to 23%, with a decrease in the melting temperature (Tm) of the membrane from 50 °C to 34 °C. Moreover, the influence of the DVB concentration on the ionic conductivity was determined for polymer electrolytes with 0, 10, 20 and 45% DVB from room temperature (RT) to 80 °C. The resulting SPEs showed a high electrochemical stability of 4.3 V as well as practical conductivity values exceeding 10−4 S cm−1 at 70 °C. Cycling performance of these semi-interpenetrated SPE’s have been shown with a Li metal polymer battery and all solid -state Li sulphur battery.

Lithium-Sulfur (Li-S) battery technology is one of the promising candidates for next generation energy storage systems. Many studies have focused on the cathode materials to improve the cell performance. In this work we present a series of poly (S-DVB) copolymers synthesised by inverse vulcanization of sulfur with divinylbenzene (DVB). The poly (S-DVB) cathode shows excellent cycling performances at C/2 and C/4 current rates, respectively. It was demonstrated poly (S-DVB) copolymer containing 20% DVB did not influence the electrochemical performance of the sulfur material, compared to elemental sulfur as high specific capacities over ∼700 mAh g −1 at 500 cycles were achieved at C/4 current rate, comparable to conventional carbon-based S cathodes. However, the use of copolymer network is assumed to act firstly as sulfur reservoir and secondly as mechanical stabilizer, enhancing significantly the cycling lifetime. The Li-poly (S-DVB) cell demonstrated an extremely low degradation rate of 0.04% per cycle achieving over 1600 cycles at C/2 current rate.

Phosphate materials became attractive electrode materials for sodium ion batteries due to their high capacity and safety properties. Cobalt iron (III) oxyphosphate CoFeOPO4@C was successfully prepared by conventional solid-state reaction at an annealing temperature of 1000 °C in air atmosphere. Our group previously reported the electrochemical properties of this material versus Li+/ Li. In this paper, we study for the first time the electrochemical activity of CoFeOPO4@C in sodium half-cells and evaluate its potential use as an anode material for sodium ion batteries. CoFeOPO4@C shows a high discharge capacity of 479 mAh g−1 at C/2 current rate over 0.01–3.0 V voltage range during the first cycle by accommodating around four sodium ions. Although the first irreversible capacity is relatively high resulting from a conversion mechanism, this phosphate can reversibly exchange about two sodium ions in the subsequent cycles, delivering a capacity of more than 200 mAh g−1 with a coulombic efficiency exceeding 97%.

Partial lithium substitution with nickel (0.25 of Ni2+ ion) in the previously reported Li1.5Fe0.5Ti1.5(PO4)3/C (LFTP@C) was performed to improve its structural and electrochemical properties. The new LiNi0.25Fe0.5Ti1.5(PO4)3/C (LNFTP@C) material was then tested as electrode for lithium ion batteries. In the voltage window 1.85V–3.0 V vs. Li+/Li, attractive electrochemical performances were obtained, mostly in terms of rate capability performance. At a current rate of 0.1C (6.6 mAg−1), the material delivered a capacity of around 120 mAhg−1, while at 5C, we observed a slight drop of the specific capacity reaching a value of 108 mAhg−1. Long-term cycling performance stability was also tested demonstrating a remarkable capacity decrease during the last 500 cycles. The capacity retention decreased from 94% to 91% after 500 cycles to about 77% and 74% after 1000 cycles at fast current rates of 5C (329.8 mAg−1) and 10C (659.6 mAg−1), respectively. In the wider voltage window, an average specific capacity of around 380 mAhg−1 was attained at a slow current rate of 0.1C.

Solid polymer electrolytes (SPEs) with new functionalized ethyl cellulose bearing a lithium/sodium fluorosulfonylimide group (Ethyl cellulose-LiFSI/NaFSI) is proposed as quasi single ion (Li+/Na+) conducting polymer electrolyte for all-solid-state lithium and sodium batteries. The degree of ethyl cellulose functionalization by anion of lithium and sodium salt measured by elemental analysis was 48 and 53%, respectively. The complex of Li(FSI-ethyl cellulose)/PEO exhibits a Li-ion transference number of TLi+ = 0.9, and a Na ion transference number of TNa+ = 0.6 for Na(FSI-ethyl cellulose),which are much higher than those reported for ambipolar LiFSI or NaFSI/PEO SPEs under the same measurement conditions. The generated SPEs showed a high electrochemical and mechanical stability as well as a practical ionic conductivity value of ~10−4 S·cm−1 at 80 °C. All solid-state lithium, sodium and Li/Sulfur cells cycled with quasi single ion conducting hybrid SPE exhibit reversible cycling and good performance at 70 °C, making them promising, environmentally benign and cost-effective candidates for use in advanced energy storage systems.

Design of novel phosphorus apatites, K2Pb6Zn2(PO4)6 and K2Pb4Ca4(PO4)6, zinc hydroxyapatite Ca8Zn2(PO4)6(OH)2, as well as hydroxyapatite Ca10(PO4)6(OH)2, and its corresponding calcined powder were conducted by means of two different synthesis protocols, i.e. solid state and wet chemical methods. The prepared materials adopt P63/m (No 176) as a space group. Structural refinements for K2Pb6Zn2(PO4)6 and K2Pb4Ca4(PO4)6 lacunar apatites, and that for the calcined hydroxyapatite, were performed using Rietveld method. For K2Pb6Zn2(PO4)6, the refinement results showed that the majority of Pb2+ cations occupy (6h) sites. This study examines the impact of the synthesis conditions on the physico-chemical properties and on the surface reactivity of the prepared materials. The analysis of the interactions of the samples with respect to a protein model (Bovin Serum Albumin), evaluated under the same experimental conditions, revealed a fast-kinetic process for the precipitated samples, compared to the crystals obtained by solid chemical reaction. Thus, the equilibrium conditions were reached in less than 20 min for the former while 6 h of contact were requested for the latter. However, all the obtained isotherms show a Langmuirian shape. The difference in the adsorption parameters of the materials, i.e. constant affinity and amount adsorbed at saturation, is discussed in terms of surface characteristics, chemical composition, crystals size and specific surface area. It is concluded that the interaction with the Bovin Serum Albumin (BSA) molecules is highly sensitive to the microstructure of the crystals.

Radiation grafted membranes with controlled monomer content were prepared to investigate the role of nitrile containing comonomers on the properties of proton conducting membranes. The membranes consist of a partially fluorinated backbone of ETFE with grafted chains containing styrene sulfonic acid and its comonomer, methacrylonitrile (MAN) or acrylonitrile (AN). Upon grafting, the comonomers show a tendency to form an alternating copolymer with styrene. The ex situ properties of both types of co-grafted membrane, i.e., proton conductivity, water uptake, and dimensional stability, are largely insensitive to the type of comonomer but mainly governed by the ion exchange capacity (IEC). Styrene/AN co-grafted membranes undergo substantial nitrile hydrolysis during the sulfonation procedure compared to styrene/MAN co-grafted membranes. The substituent at the alpha position of the comonomer determines the susceptibility of the nitrile to hydrolysis during membrane preparation as well as during fuel cell operation. Despite the change in the chemical properties as a result of hydrolysis, the mechanical integrity of the co-grafted membranes is retained. However, the styrene/AN co-grafted membrane showed considerably inferior performance in the fuel cell compared to the styrene/MAN co-grafted membrane. These findings bring about a design rationale for membrane materials with enhanced stability against hydrolysis.

We report on correlations between the proton conductivity, the water swelling and the dry-state morphology of ETFE-g-poly(sulfonated styrene-co-DVB) proton-exchange membranes (PEMs). We focus on the influence of the systematically varied monomer composition. Especially, the impact of the DVB cross-linker on the ion-rich phase aggregated in the dry PEM is studied by small-angle X-ray scattering. A modified hard-sphere fluid model describing the ion-rich phase is applied to interpret the observed scattering function. We find hereby that the size and number density of the ion-rich domains decrease with increasing cross-link level. Consequently, the distance between the ion-rich domains is proportional to the cross-link level. The total volume fraction of water in the hydrated membrane is proportional to the overall volume fraction of the ion-rich phase, and the number of water molecules per ion-rich aggregate is inversely proportional to the level of cross-linking. We show that there is a clear correlation between the structure of the ion-rich phase formed in the dry state and the proton conductivity of the hydrated membrane: beyond a threshold, indicating the onset of percolation of the aqueous network, the conductivity is proportional to the hydration level and inversely proportional to the mean distance between the ion-rich domains.

The relationships between the nano-scale structure and the monomer composition of proton exchange membranes (PEMs) are reported. The PEMs are synthesized by preirradiation-induced grafting ETFE with styrene and cross-linker, 1,3-diisopropenylbenzene (DIPB), where the styrene moieties are sulfonated subsequently. The degree of grafting is constant, while the DIPB level is varied systematically. The SAXS spectra of the dry membranes are isotropic and dominated by a single correlation peak, which results from the phase separation of the ion-rich phase from the polymer matrix. By analyzing the correlation peak we find that the number density and the typical size of the ion-rich domains decrease when the level of cross-linking is increased. The proton conductivity in the fully hydrated state is proportional to the volume fraction of the ion-rich phase. This suggests that the structure of the ion-rich phase found in the dry state has fundamental impact on the conductivity of the hydrated membrane. The relationship between the proton conductivity and the water volume fraction follows a power law in good agreement with percolation theory.

Styrene radiation grafted ETFE based proton conducting membranes are subject to degradation under fuel cell operating conditions and show a poor stability. Lifetimes exceeding 250 h can only be achieved with crosslinked membranes. In this study, a novel approach based on the increase of the intrinsic oxidative stability of uncrosslinked membranes is reported. Hence, the co-grafting of styrene with methacrylonitrile (MAN), which possesses a protected α-position and strong dipolar pendant nitrile group, onto 25 μm ETFE base film was investigated. Styrene/MAN co-grafted membranes were compared to a styrene based membrane in durability tests in single H2/O2 fuel cells. It is shown that the incorporation of MAN considerably improves the chemical stability, yielding fuel cell lifetimes exceeding 1000 h. The membrane preparation based on the co-grafting of styrene and MAN offers the prospect of tuning the MAN content and introduction of a crosslinker to enhance the oxidative stability of the resulting fuel cell membranes. Keywords: Polymer electrolyte fuel cell, Proton exchange membrane, Radiation grafting, Styrene, Methacrylonitrile, Membrane electrode assembly

Selective exposures of poly(ethylene-alt-tetrafluoroethylene) (ETFE) films with hard X-rays through high aspect ratio Ni-masks were performed at the LIGA3 beamline of the “Angstrom Quelle Karlsruhe” (ANKA) to create patterns of radicals used as initiators for the grafting of styrene into the bulk of the ETFE films. Grafted films were then sulfonated to obtain proton-conducting membranes. The structure definition, as investigated by scanning electron microscopy (SEM), showed a perfect discrimination between exposed and shaded areas through all the film thickness. Structuring results in a more homogeneous appearance of the membrane without affecting the degree of grafting and proton conductivity in the grafted areas. In fuel cell tests the structured membranes showed slightly lower performance due to 10% lower active area, but had a significantly higher lifetime.

This study concerns the investigation of the effect of reaction conditions on the radiation-induced grafting of styrene into poly(ethylene-alt-tetrafluoroethylene) base film. Grafting was obtained by the pre-irradiation method, using styrene in isopropanol/water mixture. The influence of irradiation and reaction conditions, such as irradiation dose, monomer concentration, water content of the grafting solution and reaction temperature on the grafting yield was investigated. The grafting kinetics in terms of initial polymerization rate (rp0), radical recombination rate (γ) and delay time (t0) was evaluated. It was found that the rate and the extent of grafting were strongly dependent on the grafting conditions. The order of dependence of the rate of grafting was found to be 0.46, 1.5 and 0.62 for pre-irradiation dose, monomer concentration and water content in the grafting mixture, respectively. The activation energy was determined to be 98.4 kJ/mol for the temperature range of 50–80 °C. The use of kinetic equations for the polymerization gives a useful description of the grafting process. It was determined that the initial polymerization rate and the radical recombination rate vary significantly with reaction conditions. The delay time is dependent mainly on irradiation dose and to some extent on monomer concentration.