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The deterioration of concrete sewer structures due to bio-corrosion presents critical and escalating challenges from structural, economic and environmental perspectives. Despite decades of research, this issue remains inadequately addressed, resulting in billions of dollars in maintenance costs and a shortened service life for sewer infrastructure worldwide. This challenge is exacerbated by the absence of standardized test methods and universally accepted mitigation strategies, leaving industries and stakeholders confronting an increasingly pressing problem. This paper aims to bridge this knowledge gap by providing a comprehensive review of the complex mechanisms of bio-corrosion, focusing on the formation and accumulation of hydrogen sulfide, its conversion into sulfuric acid and the subsequent deterioration of concrete materials. The paper also explores various factors affecting bio-corrosion rates, including environmental conditions, concrete properties and wastewater characteristics. The paper further highlights existing corrosion test strategies, such as chemical tests, in-situ tests and microbial simulations tests along with their general analytical parameters. The conversion of hydrogen sulfide into sulfuric acid is a primary cause of concrete decay and its progression is influenced by environmental conditions, inherent concrete characteristics, and the composition of wastewater. Through illustrative case studies, the paper assesses the practical implications and efficacy of prevailing mitigation techniques. Coating materials provide a protective barrier against corrosive agents among the discussed techniques, while optimised concrete mix designs enhance the inherent resistance and durability of the concrete matrix. Finally, this review also outlines the future prospects and challenges in bio-corrosion research with an aim to promote the creation of more resilient and cost-efficient materials for sewer systems.
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Nanocomposite coatings based on polydimethylsiloxane were developed by adding silver phosphate and titania nanoparticles with a PDMS pre-layer for 316L stainless steel. FTIR spectra and XRD patterns confirmed the synthesis of TiO2 and Ag3PO4 nanoparticles and nanocomposite coating. FESM and AFM images show that with the increase of Ag3PO4 nanoparticles, the roughness of coatings increased (Ra and Rq for adding 7 wt% of Ag3PO4 coating was 29 and 293 nm). The wettability results demonstrated that the presence of 7 wt% Ag3PO4 nanoparticles in the coating has the highest water contact angle (152 °). Nano-scratch results proved that creating a pre-layer of PDMS can increase the scratch resistance of PDMS + TiO2+Ag3PO4 nanocomposite coating (displacement and scratch coefficient were 408 nm and 0.07µΝ-1/2 with the pre-layer). Corrosion current density of 316lSS with PDMS + TiO2+Ag3PO4 coating was 0.00045 µA/cm2, while for 316LSS with pure PDMS coating was 0.00114 µA/cm2 at 37 °C in PBS solution. The Nyquist curves showed the diameter of the semicircle for the nanocomposite coating was larger than pure PDMS coating, which indicates the higher corrosion resistance of the nanocomposite coating (5.98 × 107 Ω). By increasing Ag3PO4 nanoparticles from 1 to 7 wt%, the number of E. coli bacteria in contact with the nanocomposite decreased significantly from 580000 to 31000 CFU/cm2. In the disk diffusion test, the largest inhibition zone was related to the nanocomposite coating with the addition of 7 wt% Ag3PO4 (23 mm). Therefore, the PDMS + TiO2+Ag3PO4 nanocomposite coating has improved properties such as superhydrophobicity, advanced mechanical behavior, bio-corrosion resistance, and antibacterial activity.
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Materiales Biocompatibles Revestidos , Nanocompuestos , Materiales Biocompatibles Revestidos/farmacología , Materiales Biocompatibles Revestidos/química , Corrosión , Escherichia coli , Nanocompuestos/química , Antibacterianos/farmacologíaRESUMEN
High-entropy alloys (HEA) with superior biocompatibility, high pitting resistance, minimal debris accumulation, and reduced release of metallic ions into surrounding tissues are potential replacements for traditional metallic bio-implants. A novel equiatomic HEA based on biocompatible metals, CrMoNbTiZr, was consolidated by spark plasma sintering (SPS). The relative sintered density of the alloy was about 97% of the theoretical density, indicating the suitability of the SPS technique to produce relatively dense material. The microstructure of the sintered HEA consisted of a BCC matrix and Laves phase, corresponding to the prediction of the thermodynamic CALPHAD simulation. The HEA exhibited a global Vickers microhardness of 531.5 ± 99.7 HV, while the individual BCC and Laves phases had hardness values of 364.6 ± 99.4 and 641.8 ± 63.0 HV, respectively. Its ultimate compressive and compressive yield strengths were 1235.7 ± 42.8 MPa and 1110.8 ± 78.6 MPa, respectively. The elasticity modulus of 34.9 ± 2.9 GPa of the HEA alloy was well within the range of cortical bone and significantly lower than the values reported for commonly used biomaterials made from Ti-based and Cr-Co-based alloys. In addition, the alloy exhibited good resistance to bio-corrosion in PBS and Hanks solutions. The CrMoNbTiZr HEA exhibited an average COF of 0.43 ± 0.06, characterized mainly by abrasive and adhesive wear mechanisms. The CrMoNbTiZr alloy's mechanical, bio-corrosion, and wear resistance properties developed in this study showed a good propensity for application as a biomaterial.
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The increasing global demand for fatty products, population growth, and the expansion of food service establishments (FSEs) present significant challenges for the wastewater industry. This is often due to the build-up of fat, oil and grease (FOG) in sewers, which reduces capacity and leads to sanitary sewer overflows. It is crucial to develop economic and sustainable in-sewer FOG management techniques to minimise maintenance costs and service disruptions caused by the removal of FOG deposits from sewers. This study aims to understand the process of FOG deposit formation in both concrete and non-concrete sewers. Compared to fresh cooking oil, disposal of used cooking oil in households and FSE sinks results in the formation of highly adhesive and viscous FOG deposits. This occurs due to hydrolysis during frying, which increases the concentration of fatty acids, particularly palmitic acid, in the used cooking oil. Furthermore, metal ions from food waste, wastewater, and dishwashing detergents contribute to the saponification and aggregation reactions which cause FOG deposition in both concrete and non-concrete sewers. However, the leaching of Ca2+ ions exacerbates FOG deposition in cement-concrete sewers. The article concludes by suggesting future research perspectives and proposes implementation strategies for microbially induced concrete corrosion (MICC) control to manage FOG deposition in sewers. One such strategy involves applying superhydrophobic coating materials with low surface free energy and high surface roughness to the interior surfaces of the sewer. This approach would help repel wastewater carrying FOG deposit components, potentially disrupting the interaction between FOG components, and reducing the adhesion of FOG deposits to sewer surfaces.
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The present work investigated biocompatibility of the unique nanostructural surface morphology inherently evolved in laser-based additively manufactured CoCrMo after biocorrosion in simulated body fluid at physiological temperature (37 °C). The extremely rapid thermokinetics intrinsically associated with the laser-based additive manufacturing technique resulted in heterogeneous cellular dendritic solidification morphologies with selective elemental segregation along the cell boundaries within CoCrMo samples. Consequently, a selective and spatially varying electrochemical response resulted in generation of a nanoscale surface morphology (crests and troughs) due to differential localized electrochemical etching. Also, depth of the trough regions was a function of the applied potential difference during potentiodynamic polarization which resulted in samples with varying morphological ratio (depth of trough/width of cell wall). CoCrMo with such nanoscale surface undulations were proposed for enhanced biocompatibility in terms of viability, spreading, and integration of MT3C3 pre-osteoblasts cells elucidated via MTT assay, immunofluorescence, and microscopy techniques. Furthermore, the influence of the morphological ratio, characteristic to the additively deposited CoCrMo after electrochemical etching (biocorrosion) on biocompatibility of MT3C3 pre-osteoblasts cells was qualitatively and quantitatively compared to a mirror-polished flat CoCrMo surface.
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Aleaciones , Rayos Láser , TemperaturaRESUMEN
Sulfate-reducing bacteria (SRB) have impacted the biocorrosion process for various industrial sectors, especially in the oil and gas industry. The higher stability over extreme conditions is the key parameter for their survival in such environments. So far, many materials have been tried to minimize or control the growth of SRB. In the present study, an organo-metallic compound of the zinc sorbate (ZS) was successfully synthesized by the simple co-precipitation method and its improved antibacterial activity against SRB. The SRB consortia are enriched from the sub-surface soil sample and identified by 16s rDNA sequencing by targeting the V3-V4 region. The most dominating genera identified with sulfate-reducing capability are Sulfurospirillum (42 %), Shewanella (19 %) Bacteroides (14 %), and Desulfovibrio (8 %). Further biocorrosion experiments are conducted by weight loss methods. Higher corrosion current density (Icorr) and less charge transfer resistance (Rct) are observed for the SRB consortia. Concurrently, higher Rct is kept for the inhibitor-included systems. The slowest release of the sorbate into the medium suppressed the growth of the SRB bacterial cells with 86 ± 3 % corrosion inhibition efficiency and prevented further corrosion reactions by forming a protective layer over the surface of the carbon steel API 5LX. The surface analysis strongly confirmed that SRB caused pitting corrosion, which has been suppressed in the inhibitor-included systems.
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Biopelículas , Desulfovibrio , Corrosión , Acero , SulfatosRESUMEN
Implantation is an essential issue in orthopedic surgery. Bulk metallic glasses (BMGs), as a kind of novel materials, attract lots of attentions in biological field owing to their comprehensive excellent properties. Here, we show that a Zr61Ti2Cu25Al12 (at. %) BMG (Zr-based BMG) displays the best cytocompatibility, pronounced positive effects on cellular migration, and tube formation from in-vitro tests as compared to those of commercial-pure titanium and poly-ether-ether-ketone. The in-vivo micro-CT and histological evaluation demonstrate the Zr-based BMG can significantly promote a bone formation. Immunofluorescence tests and digital reconstructed radiographs manifest a stimulated effect on early blood vessel formation from the Zr-based BMG. Accordingly, the intimate connection and coupling effect between angiogenesis and osteogenesis must be effective during bone regeneration after implanting Zr-based BMG. Dynamic gait analysis in rats after implanting Zr-based BMG demonstrates a tendency to decrease the pain level during recovery, simultaneously, without abnormal ionic accumulation and inflammatory reactions. Considering suitable mechanical properties, we provide a realistic candidate of the Zr61Ti2Cu25Al12 BMG for biomedical applications.
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Magnesium-zinc-calcium (Mg-Zn-Ca) alloys as a biomaterial have attracted much attention recently, owing to their excellent biocompatibility, similar mechanical properties to natural bone, and biodegradable properties. Despite the numerous advantages of MgZnCa alloys, the rapid degradation of magnesium proved challenging as the implant in unable to retain its structural integrity for a sufficient duration of time. For metallic glasses, the capability to produce a bulk sample that is sufficiently large for useful applications have been far less successful owing to challenging processing parameters that are required for rapid cooling. In this study, Mg65Zn30Ca5 melt-spun ribbons were produced using melt-spinning followed by spark plasma sintering under high pressure (60 MPa) at different temperatures (130-170 °C) to provide an insight into the consolidation, mechanical, and corrosion behavior. Microstructural interfaces were characterized using scanning electron microscopy while the thermal stability of the amorphous phase was characterized using differential scanning calorimetry and X-ray diffraction. Here, pellets with 10 mm diameter and 10 mm height with a complete amorphous structure were achieved at a sintering temperature of 150 °C with densification as high at ~98%. Sintering at higher temperatures, while achieving higher densification, resulted in the presence of nano-crystallites. The mechanical properties were characterized using microhardness and compression tests. The hardness values of the sintered products were relatively higher to those containing crystallite phases while the ultimate compressive strength increased with increasing sintering temperature. Bio-corrosion properties were characterized via electrochemical testing with PBS as the electrolyte at 37 °C. The corrosion results suggest that the sintered samples have a significantly improved corrosion resistance as compared to as-cast samples. More notably, SPS150 (samples sintered at 150 °C) exhibited the best corrosion resistance (35× compared to as-cast in the context of corrosion current density), owing to its single-phase amorphous nature. This study clearly shows the potential of spark plasma sintering in consolidating amorphous ribbons to near-full density bulk pellets with high corrosion resistance for bio-applications.
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The MgCa0.7 alloy may be a promising material for biodegradable surgical wires. In this paper, the technology for producing surgical wires from this alloy has been developed, based both on finite element modelling and experimental study. In particular, the extrusion and hot-drawing effects on the mechanical properties, microstructures, in-vitro rates of biocorrosion, and cytotoxicity to human cancer cells (SaOS-2) and healthy (hPDL) ones, have been determined. An approximately 30-40% increase in corrosion rate due to increasing hot-drawing temperature was observed. An effect of hot-drawing temperature on cytotoxicity was also found. Notably, at various stages of the final wires' production, the MgCa0.7 alloy became toxic to cancer cells. This cytotoxicity depended on the alloys' processing parameters and was maximal for the as-extruded rod and for the wires immediately after hot drawing at 440 °C. Thus, the careful selection of processing parameters makes it possible to obtain a product that is not only a promising candidate for biodegradable surgical wires, but one which also has intrinsic bioactive properties that produce antitumor activity.
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Ti-Si-xCu coatings (TS-xC,x= 5, 10 and 15 wt.%) with advanced bio-corrosion resistance, excellent antibacterial property and biocompatibility were laser cladded on Ti-6Al-4V (TAV) substrate which is widely used as endosseous implants. The bio-corrosion resistance of the TAV substrate was improved due to the presence of Ti5Si3and TiCu phases in the coatings. The addition of Cu in the precursor contributes to the improvement of the antibacterial property of TAV substrate. Meanwhile, induced normal cytoskeleton, well-developed focal adhesion contacts, significant higher cell attachment and proliferation rate were observed for the TS-xC coated samples due to the formation of micro-textured morphology and presence of new phases. The bio-corrosion resistance and antibacterial property depend on Cu content addition in the TS-xC precursor. The results provide a way to fabricate such multiple functional biocoating that would improve the bio-corrosion resistance, antibacterial performance and biocompatibility of TAV.
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Aleaciones , Antibacterianos , Materiales Biocompatibles Revestidos , Osteoblastos/efectos de los fármacos , Titanio , Aleaciones/química , Aleaciones/farmacología , Animales , Antibacterianos/química , Antibacterianos/farmacología , Bacterias/efectos de los fármacos , Línea Celular , Proliferación Celular/efectos de los fármacos , Materiales Biocompatibles Revestidos/química , Materiales Biocompatibles Revestidos/farmacología , Rayos Láser , Metales/química , Metales/farmacología , Ratones , Propiedades de Superficie , Titanio/química , Titanio/farmacologíaRESUMEN
The Microbiologically Induced Corrosion (MIC) of concrete sewer pipes is a commonly known problem that can lead to the destruction of the system, creating multiple public health issues and the need for costly repair investments. The present study focuses on the development of a magnesium hydroxide coating, with optimized properties to protect concrete against MIC. The anti-corrosion properties of the respective coating were evaluated by using short and long duration accelerated sulfuric acid spraying tests. The coating presented satisfying adhesion ability, based on pull-off and Scanning Electron Microscopy (SEM) analysis measurements. The surface pH of the coated concrete was maintained at the alkaline region (i.e., >8.0) throughout the duration of all acid spraying tests. The consumption of the coating, due to the reaction (neutralization) with sulfuric acid, was confirmed by the respective mass and thickness measurements. The protection ability of this coating was also evaluated by recording the formation of gypsum (i.e., the main corrosion product of concrete) during the performed tests, by X-ray Diffraction (XRD) analysis and by the Attenuated Total Reflectance (ATR) measurements. Finally, a long duration acid spraying test was additionally used to evaluate the behavior of the coating, simulating better the conditions existing in a real sewer pipe, and the obtained results showed that this coating is capable of offering prolonged protection to the concrete substrate.
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Magnesium and its alloys have been considered for consumable bio-implant applications due to their similar mechanical properties to the natural bone and biodegradability. Nevertheless, uncontrollable corrosion rate and limited bioactivity of Mg based materials in biological environment restrain their application. In light of this, objective of the present study was to explore addition of hydroxyapatite (HA, Ca10(PO4)6OH2), a ceramic similar to bone mineral, into AZ31B Mg alloy and its effects on bio-corrosion behavior. Friction stir processing based additive manufacturing route was employed for producing AZ31B Mg-HA composites. Various HA contents (5, 10, and 20 wt%) were incorporated into Mg matrix. The microstructural observation revealed that the size of α-Mg grains reduced significantly after friction stir process. HA incorporation took place at micro/nanoscale in α-Mg matrix under the thermo-mechanical forces exerted by friction stir process. The corrosion behavior of friction stir processed Mg-HA composites was investigated using electrochemical methods in simulated body fluid. The results indicated an improvement in corrosion resistance for the composites compared to untreated AZ31B which was attributed to significant grain refinement upon friction stir process. On the other hand, incremental addition of HA had an opposing effect due to localized micro/nano-galvanic couples. As a result, friction stir process Mg-5 wt% HA composite demonstrated the highest corrosion resistance due to an optimum balance between beneficial effects of grain size refinement and limited number of local galvanic couples compared to the other friction stir process samples explored in the present work.
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Aleaciones/química , Materiales Biocompatibles/química , Durapatita/química , Magnesio/química , CorrosiónRESUMEN
Owing to its good biocompatibility and low cost, stainless steel is one of the most widely utilized biomaterial. However, longtime assessment of stainless steel has shown problems related to material degradation, especially localized corrosion and bio-film formation. In addition, the leaching of toxic nickel and chromium ions from stainless steel leads to additional health complications. Here, we utilized submerged friction stir processing, a severe surface deformation technique for significantly enhancing its durability, bio-activity as well as antibacterial resistance. The processing was done with a wide variation in strain rates to produce tunable surface microstructure. High strain-rate processing resulted in nearly single-phase fine-grained microstructure, while slow strain-rate processing developed a dual-phase fine-grained microstructure. The bio-corrosion rate of processed steel was reduced by more than 60 % along with significant enhancement in the pitting resistance. The processed steel showed nearly no bacterial adhesion/biofilm formation, evaluated using S. aureus and E. coli bacterial strains. Further, the processed stainless steel surface demonstrated minimum leaching of the toxic elements, significantly enhancing its appeal for bio-implant applications. The observed behavior was explained based on the formation of a stable passive layer, rich in Cr2O3, as determined using x-ray photoelectron microscopy (XPS) and increased hydrophilicity.
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Escherichia coli , Acero Inoxidable , Corrosión , Fricción , Staphylococcus aureusRESUMEN
The removal of tumors in the osseous tissue leads to functional disorders. To overcome this issue, biodegradable implants are used to replace the damaged part of the system. In the study, samarium oxide was coated on the anodic layer of AZ31 magnesium alloy. The potentiodynamic polarization, electrochemical impedance, and localized electrochemical impedance spectroscopy studies were carried out for the samarium-coated magnesium alloy. The corrosion resistance of the coating improved several folds than the bare alloy. The apatite formed on the 3rd day of immersion in the simulated body fluid showed cuboid and triangular structures, whereas on the 7th day, it exhibited a sea sponge-like appearance. The coating exhibited inherent anticancer and antibacterial properties. Our work suggests that the samarium coating is expected to be a promising orthopedic implant for preventing tumor relapse and metastasis.
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Fast degradation rate and inhomogeneous corrosion are obstacles for magnesium alloy bio-corrosion properties. In this paper, a quaternary Mg-Zn-Ca-Mn alloy was designed by an orthogonal method and prepared by vacuum induction melting to investigate its bio-corrosion. Microstructure, corrosion morphology, and bio-corrosion properties of as-cast alloys 1 to 5 with good corrosion resistance were characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray diffraction with immersion and electrochemical tests in simulated body fluid (SBF), respectively. Both the orthogonal method and in vitro degradation experiments demonstrated that alloy 3 exhibited the lowest degradation rate among the tested quaternary Mg-Zn-Ca-Mn alloys. Then, as-cast alloy 3 was treated by solid-solution and solid-solution aging. In vitro experimental results indicated that as-cast alloy 3 showed better corrosion resistance than heat-treated specimens and the average corrosion rate was approximately 0.15 mm/y. Heat-treated alloy 3 exhibited more uniform corrosion than as-cast alloy specimens. These results suggest that alloy 3 has the potential to become a biodegradable candidate material.
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Aleaciones/química , Soluciones/química , Líquidos Corporales/química , Calcio/química , Corrosión , Técnicas Electroquímicas , Magnesio/química , Manganeso/química , Microscopía Electrónica de Rastreo , Espectrometría por Rayos X , Temperatura , Vacio , Zinc/químicaRESUMEN
AIM: To investigate the molecular structural disorders of cancerous skin. MATERIALS AND METHODS: Human malignant melanoma and basal cell carcinoma biopsies were used for the investigation. Fourier transform infrared (FT-IR), Raman spectroscopy, and scanning electron microscopy were utilized. Spectral differences between healthy, basal cell carcinoma and melanoma tissues were recorded. RESULTS: The FT-IR bands of vasCH2, vsCH2 and Raman vsCH3 of cell membrane lipids were increased in intensity in melanoma due to an increased lipophilic environment. The FT-IR band at 1,744 cm-1 assigned to malondialdehyde can be used as a band diagnostic of cancer progression. The amide I bands at 1,654 cm-1 and 1,650 cm-1 for Raman and FT-IR, respectively were broader in spectra from melanoma, reflecting changes of protein secondary structure from α-helix to ß-sheet and random coil. The intensity of the FT-IR band at 1,046 cm-1 was increased in melanoma, suggesting glycosylation of the skin upon cancer development. Another band that might be considered as diagnostic was found at about 815 cm-1 in melanoma and was attributed to Z-DNA configuration. As far as we know, this is the first time that scanning electron microscopy revealed that metal components of titanium alloys from tooth implants were transferred to melanoma tissue taken from the back of one patient. CONCLUSION: Vibrational spectroscopy highlighted increased glycosylation in melanoma.
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Carcinoma Basocelular/química , Melanoma/química , Proteínas de Neoplasias/química , Neoplasias Cutáneas/química , Anciano , Biopsia , Carcinoma Basocelular/patología , Humanos , Malondialdehído/química , Melanoma/patología , Persona de Mediana Edad , Estructura Secundaria de Proteína , Piel/química , Piel/patología , Neoplasias Cutáneas/patología , Espectroscopía Infrarroja por Transformada de Fourier , Espectrometría Raman , Melanoma Cutáneo MalignoRESUMEN
Due to their desirable elastic modulus and density that are similar to natural bone, non-toxic element containing magnesium alloys are regarded as promising bio-degradable materials. A biodegradable HA-particle-reinforced magnesium-matrix composite Mg-3Zn-0.2Ca-1HA (wt%) was fabricated for biomedical application by a combination of high shear solidification (HSS) and hot extrusion technology. The microstructure, mechanical properties, corrosion resistance and cell biocompatibility of the composite were subsequently investigated. In comparison with the matrix alloy, the as-cast Mg-3Zn-0.2Ca-1HA composite obtained by HSS technology exhibited a uniform and fine grained structure, further refined after a hot extrusion ratio of 36:1. The yield strength (0.2%YS), ultimate tensile strength and elongation of the extruded composite were 322â¯MPa, 341â¯MPa and 7.6%, respectively. The corrosion rate of the as-extruded Mg-3Zn-0.2Ca-1HA composite was measured to be 1.52â¯mm/y. Electrochemical and immersion tests showed that the corrosion resistance of the composite is slightly improved comparing to that of the matrix alloy.
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Aleaciones/química , Materiales Biocompatibles/química , Durapatita/química , Magnesio/química , Zinc/química , Animales , Línea Celular , Corrosión , Fibroblastos/citología , Ensayo de Materiales , Ratones , Resistencia a la TracciónRESUMEN
Magnesium is an attractive biodegradable material for medical applications due to its non-toxicity, low density and good mechanical properties. The fast degradation rate of magnesium can be tailored using alloy design. The combined addition of Sr and Ca results in a good combination of mechanical and corrosion properties; the alloy compositions with the best performance are Mg-0.5Sr and Mg-0.3Sr-0.3Ca. In this study, we investigated an important effect, namely thermal treatment (at 400 °C), on alloy properties. The bio-corrosion of the alloys was analyzed via in vitro corrosion tests in simulated body fluid (SBF); the mechanical properties were studied through tensile, compression and three-point bending tests in two alloy conditions, as-cast and heat-treated. We showed that 8h of heat treatment increases the corrosion rate of Mg-0.5Sr very rapidly and decreases its mechanical strength. The same treatment does not significantly change the properties of Mg-0.3Sr-0.3Ca. An in-depth microstructural investigation via transmission electron microscopy, scanning electron microscopy, electron probe micro-analysis and X-ray diffraction elucidated the effects of the thermal exposure. Microstructural characterization revealed that Mg-0.3Sr-0.3Ca has a new intermetallic phase that is stable after 8h of thermal treatment. Longer thermal exposure (24h) leads to the dissolution of this phase and to its gradual transformation to the equilibrium phase Mg17Sr2, as well as to a loss of mechanical and corrosion properties. The ternary alloy shows better thermal stability than the binary alloy, but the manufacturing processes should aim to not exceed exposure to high temperatures (400 °C) for prolonged periods (over 24 h).
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Implantes Absorbibles , Aleaciones/química , Materiales Biocompatibles/química , Calcio/química , Calor , Ensayo de Materiales , Modelos Biológicos , Propiedades de SuperficieRESUMEN
The combination of solid solution heat treatments and severe plastic deformation by high-ratio differential speed rolling (HRDSR) resulted in the formation of an ultrafine-grained microstructure with high thermal stability in a Mg-5Zn-0.5Zr (ZK60) alloy. When the precipitate particle distribution was uniform in the matrix, the internal stresses and dislocation density could be effectively removed without significant grain growth during the annealing treatment (after HRDSR), leading to enhancement of corrosion resistance. When the particle distribution was non-uniform, rapid grain growth occurred in local areas where the particle density was low during annealing, leading to development of a bimodal grain size distribution. The bimodal grain size distribution accelerated corrosion by forming a galvanic corrosion couple between the fine-grained and coarse-grained regions. The HRDSR-processed ZK60 alloy with high thermal stability exhibited high corrosion resistance, high strength and high ductility, and excellent superplasticity, which allow the fabrication of biodegradable magnesium devices with complicated designs that have a high mechanical integrity throughout the service life in the human body.
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Aleaciones/química , Calor , Fenómenos Mecánicos , CorrosiónRESUMEN
Low density, non-toxicity, biodegradability and mechanical properties similar to human tissues such as bone make magnesium (Mg) alloys attractive for biomedical applications ranging from bone to cardiovascular implants. The most important challenge that still prevents the widespread use of Mg implants is their rapid degradation rate. In this study we investigate the combined effect of calcium (Ca) and strontium (Sr) on the corrosion behavior of Mg via in vitro immersion and electrochemical tests in simulated body fluid (SBF), and analyze changes in mechanical properties. We show that the combined addition of 0.3 wt.% Sr and 0.4 wt.% Ca decreases the corrosion rate of Mg both in terms of mass loss and hydrogen evolution more effectively than the single addition of either alloying element. We investigate the microstructure of as-cast specimens and the morphology of the corrosion products using optical microscopy, scanning electron microscopy, electron probe micro-analysis, X-ray diffraction, and X-ray photoelectron spectroscopy. Tensile and three point bending tests reveal that the ternary alloy Mg-0.3Sr-0.3Ca has a good combination of mechanical properties and corrosion resistance with hydrogen evolution rates of 0.01 mL/cm(2)/h in SBF. Higher concentrations of Sr and Ca alter the resulting microstructure leading to increased corrosion rates in SBF by promoting the micro-galvanic corrosion between the α-Mg matrix and intermetallic phases of Mg17Sr2 and Mg2Ca along the grain boundaries. These results indicate that the combined addition of optimal amounts of Ca and Sr is a promising approach to decrease the high degradation rate of Mg implants in physiological conditions, as well as attaining high ductility in the alloy. The better properties of the Mg-0.3Sr-0.3Ca alloy are related to the new intermetallic phases found in this sample. The optimum composition is attributed to the "third element effect", as seen in the corrosion behavior of metallic alloys.