Munsu Kim, L. Perez-Andrade, Luke N. Brewer, G. Kubacki
This paper investigates the effect of the microstructure on the corrosion behavior of cold sprayed (CS) AA5083 compared to its wrought counterpart. It has been shown that the microstructure of CS aluminum alloys, such as AA2024, AA6061, and AA7075, affects their corrosion behavior; however, investigations of the corrosion behavior of CS AA5083 with a direct comparison to wrought AA5083 have been limited. The microstructure and corrosion behavior of CS AA5083 were examined by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), electron backscattered diffraction (EBSD), electrochemical and immersion tests, and ASTM G67. The CS process resulted in microstructural changes, such as the size and spatial distribution of intermetallic particles, grain size, and misorientation. The refined grain size and intermetallic particles along prior particle boundaries stimulated the initiation and propagation of localized corrosion. Electrochemical tests presented enhanced anodic kinetics with high pitting susceptibility, giving rise to extensive localized corrosion in CS AA5083. The ASTM G67 test demonstrated significantly higher mass loss for CS AA5083 compared to its wrought counterpart due to preferential attack within prior particle boundary regions in the CS microstructure. Possible mechanisms of intergranular corrosion (IGC) propagation at prior particle boundary regions have been discussed.
{"title":"Effect of Microstructure on Corrosion Behavior of Cold Sprayed Aluminum Alloy 5083","authors":"Munsu Kim, L. Perez-Andrade, Luke N. Brewer, G. Kubacki","doi":"10.3390/cmd5010002","DOIUrl":"https://doi.org/10.3390/cmd5010002","url":null,"abstract":"This paper investigates the effect of the microstructure on the corrosion behavior of cold sprayed (CS) AA5083 compared to its wrought counterpart. It has been shown that the microstructure of CS aluminum alloys, such as AA2024, AA6061, and AA7075, affects their corrosion behavior; however, investigations of the corrosion behavior of CS AA5083 with a direct comparison to wrought AA5083 have been limited. The microstructure and corrosion behavior of CS AA5083 were examined by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), electron backscattered diffraction (EBSD), electrochemical and immersion tests, and ASTM G67. The CS process resulted in microstructural changes, such as the size and spatial distribution of intermetallic particles, grain size, and misorientation. The refined grain size and intermetallic particles along prior particle boundaries stimulated the initiation and propagation of localized corrosion. Electrochemical tests presented enhanced anodic kinetics with high pitting susceptibility, giving rise to extensive localized corrosion in CS AA5083. The ASTM G67 test demonstrated significantly higher mass loss for CS AA5083 compared to its wrought counterpart due to preferential attack within prior particle boundary regions in the CS microstructure. Possible mechanisms of intergranular corrosion (IGC) propagation at prior particle boundary regions have been discussed.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":" 3","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139619185","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
K. Duncan, Lina E. Dominici, M. Nanny, I. Davidova, Brian H. Harriman, J. M. Suflita
Some naval vessels add seawater to carbon steel fuel ballast tanks to maintain stability during fuel consumption. Marine sediments often contaminate ballast tank fluids and have been implicated in stimulating fuel biodegradation and enhancing biocorrosion. The impact of the marine sediment was evaluated in model ballast tank reactors containing seawater, fuel (petroleum-F76, Fischer–Tropsch F76, or a 1:1 mixture), and carbon steel coupons. Control reactors did not receive fuel. The marine sediment was added to the reactors after 400 days and incubated for another year. Sediment addition produced higher estimated bacterial numbers and enhanced sulfate reduction. Ferrous sulfides were detected on all coupons, but pitting corrosion was only identified on coupons exposed to FT-F76. Aerobic hydrocarbon-degrading bacteria increased, and the level of dissolved iron decreased, consistent with the stimulation of aerobic hydrocarbon degradation by iron. We propose that sediments provide an inoculum of hydrocarbon-degrading microbes that are stimulated by dissolved iron released during steel corrosion. Hydrocarbon degradation provides intermediates for use by sulfate-reducing bacteria and reduces the level of fuel components inhibitory to anaerobic bacteria. The synergistic effect of dissolved iron produced by corrosion, biodegradable fuels, and iron-stimulated hydrocarbon-degrading microbes is a poorly recognized but potentially significant biocorrosion mechanism.
{"title":"Microbial Communities in Model Seawater-Compensated Fuel Ballast Tanks: Biodegradation and Biocorrosion Stimulated by Marine Sediments","authors":"K. Duncan, Lina E. Dominici, M. Nanny, I. Davidova, Brian H. Harriman, J. M. Suflita","doi":"10.3390/cmd5010001","DOIUrl":"https://doi.org/10.3390/cmd5010001","url":null,"abstract":"Some naval vessels add seawater to carbon steel fuel ballast tanks to maintain stability during fuel consumption. Marine sediments often contaminate ballast tank fluids and have been implicated in stimulating fuel biodegradation and enhancing biocorrosion. The impact of the marine sediment was evaluated in model ballast tank reactors containing seawater, fuel (petroleum-F76, Fischer–Tropsch F76, or a 1:1 mixture), and carbon steel coupons. Control reactors did not receive fuel. The marine sediment was added to the reactors after 400 days and incubated for another year. Sediment addition produced higher estimated bacterial numbers and enhanced sulfate reduction. Ferrous sulfides were detected on all coupons, but pitting corrosion was only identified on coupons exposed to FT-F76. Aerobic hydrocarbon-degrading bacteria increased, and the level of dissolved iron decreased, consistent with the stimulation of aerobic hydrocarbon degradation by iron. We propose that sediments provide an inoculum of hydrocarbon-degrading microbes that are stimulated by dissolved iron released during steel corrosion. Hydrocarbon degradation provides intermediates for use by sulfate-reducing bacteria and reduces the level of fuel components inhibitory to anaerobic bacteria. The synergistic effect of dissolved iron produced by corrosion, biodegradable fuels, and iron-stimulated hydrocarbon-degrading microbes is a poorly recognized but potentially significant biocorrosion mechanism.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"29 42","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139388717","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In this paper, time/frequency domain data processing was proposed to analyse the EN signal recorded during stress corrosion cracking on precipitation-hardening martensitic stainless steel in a chloride environment. Continuous Wavelet Transform, albeit with some limitations, showed a suitable support in the discriminatory capacity among transient signals related to the different stress corrosion cracking mechanisms. In particular, the aim is to propose the analysis of electrochemical noise signals under stress corrosion cracking conditions in the time–frequency domain by using the Hilbert–Huang approach. The Hilbert–Huang Transform (performed by the Empirical Mode Decomposition approach) was finally proposed to carry out an identification of the corrosion mechanisms in comparison to conventional data processing methods. By using this approach, a detailed simultaneous decomposition of the original electrochemical noise data in the time and frequency domain was carried out. The method gave useful information about transitions among different corrosion mechanisms, allowing us to (i) identify a specific characteristic response for each corrosion damaging phenomenon induced by stress corrosion cracking, (ii) time each corrosion of the damaging phenomenon, and (iii) provide a topological description of the advancing SCC damaging stages. This characteristic evidences that the Hilbert–Huang Transform is a very powerful technique to potentially recognize and distinguish the different corrosion mechanisms occurring during stress corrosion cracking.
{"title":"Data Mining Applied to the Electrochemical Noise Technique in the Time/Frequency Domain for Stress Corrosion Cracking Recognition","authors":"L. Calabrese, M. Galeano, E. Proverbio","doi":"10.3390/cmd4040034","DOIUrl":"https://doi.org/10.3390/cmd4040034","url":null,"abstract":"In this paper, time/frequency domain data processing was proposed to analyse the EN signal recorded during stress corrosion cracking on precipitation-hardening martensitic stainless steel in a chloride environment. Continuous Wavelet Transform, albeit with some limitations, showed a suitable support in the discriminatory capacity among transient signals related to the different stress corrosion cracking mechanisms. In particular, the aim is to propose the analysis of electrochemical noise signals under stress corrosion cracking conditions in the time–frequency domain by using the Hilbert–Huang approach. The Hilbert–Huang Transform (performed by the Empirical Mode Decomposition approach) was finally proposed to carry out an identification of the corrosion mechanisms in comparison to conventional data processing methods. By using this approach, a detailed simultaneous decomposition of the original electrochemical noise data in the time and frequency domain was carried out. The method gave useful information about transitions among different corrosion mechanisms, allowing us to (i) identify a specific characteristic response for each corrosion damaging phenomenon induced by stress corrosion cracking, (ii) time each corrosion of the damaging phenomenon, and (iii) provide a topological description of the advancing SCC damaging stages. This characteristic evidences that the Hilbert–Huang Transform is a very powerful technique to potentially recognize and distinguish the different corrosion mechanisms occurring during stress corrosion cracking.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"2 20","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138595714","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
When introduced into the body, the implant interacts with biological environment and may suffer corrosion. In addition, when this implant is submitted to friction, it may degrade by tribocorrosion due to the simultaneous action of corrosion by the body liquid and mechanical wear. Both corrosion and tribocorrosion are connected to the presence of proteins that cover the surface implant. The latter plays an ambiguous role on corrosion since dozens of contradictory papers pointed out their beneficial or detrimental effect. After its introduction into the body, the implant should form a direct interface with bone through structural and functional connection. The osseointegration and the strength of interfacial bond depend on surface properties of the implant, namely, its topographical and physico-chemical properties. In addition, since bone cells are sensitive to the species produced during the implant corrosion, when corrosion occurs, this may lead to impact osseointegration and to cause implant loosening. There is a strong connection between corrosion and osseointegration, both of which are worth discussion. That is the object of the present narrative review where we will discuss: (1) corrosion and tribocorrosion of titanium alloys used as biomaterials paying particular attention to the influence of proteins, (2) the effect of implant roughness and surface energy on osseointegration.
{"title":"Review on Corrosion, Tribocorrosion and Osseointegration of Titanium Alloys as Biomaterials","authors":"Jamal Takadoum","doi":"10.3390/cmd4040033","DOIUrl":"https://doi.org/10.3390/cmd4040033","url":null,"abstract":"When introduced into the body, the implant interacts with biological environment and may suffer corrosion. In addition, when this implant is submitted to friction, it may degrade by tribocorrosion due to the simultaneous action of corrosion by the body liquid and mechanical wear. Both corrosion and tribocorrosion are connected to the presence of proteins that cover the surface implant. The latter plays an ambiguous role on corrosion since dozens of contradictory papers pointed out their beneficial or detrimental effect. After its introduction into the body, the implant should form a direct interface with bone through structural and functional connection. The osseointegration and the strength of interfacial bond depend on surface properties of the implant, namely, its topographical and physico-chemical properties. In addition, since bone cells are sensitive to the species produced during the implant corrosion, when corrosion occurs, this may lead to impact osseointegration and to cause implant loosening. There is a strong connection between corrosion and osseointegration, both of which are worth discussion. That is the object of the present narrative review where we will discuss: (1) corrosion and tribocorrosion of titanium alloys used as biomaterials paying particular attention to the influence of proteins, (2) the effect of implant roughness and surface energy on osseointegration.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"26 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139224760","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ezazul Haque Sabuz, Mohammed Noor-A-Alam, Waseem Haider, Ishraq Shabib
In this study, mechanical and electrochemical performance of borided additively manufactured (AM) and wrought 8620 low alloy steel were investigated and compared to their bare counterparts. The microstructure of borided 8620 exhibited the presence of FeB and Fe2B phases with a saw tooth morphology. Both AM and wrought samples with boride layers showed a similar performance in hardness, wear, potentiodynamic polarization (PD), electrochemical impedance spectroscopy (EIS), and linear polarization resistance (LPR) experiments. However, borided steels exhibited about an 8-fold increase in Vickers hardness and about a 6-fold enhancement in wear resistance compared to bare ones. Electrochemical experiments of borided specimens (both AM and wrought) in 0.1 M Na2S2O3 + 1 M NH4Cl solution revealed a 3–6-fold lower corrosion current density, about a 6-fold higher charge transfer resistance, and about a 6-fold lower double-layer capacitance, demonstrating an improved corrosion resistance compared to their bare counterparts. Post-corrosion surface analysis revealed the presence of thick sulfide and oxide layers on the bare steels, whereas dispersed corrosion particles were observed on the borided samples. The enhanced wear and electrochemical performance of the borided steels were attributed to the hard FeB/Fe2B layers and the reduced amount of adsorbed sulfur on their surface.
本文研究了8620低合金钢的力学性能和电化学性能，并与裸合金钢进行了比较。渗硼8620的显微组织表现为具有锯齿状形貌的FeB和Fe2B相。在硬度、磨损、动电位极化(PD)、电化学阻抗谱(EIS)和线性极化电阻(LPR)实验中，AM和变形后的硼化物层样品表现出相似的性能。然而，与裸钢相比，渗硼钢的维氏硬度提高了8倍，耐磨性提高了6倍。在0.1 M Na2S2O3 + 1 M NH4Cl溶液中进行的电化学实验表明，与裸样品相比，带硼试样(AM和变形试样)的腐蚀电流密度降低了3 - 6倍，电荷转移电阻提高了约6倍，双层电容降低了约6倍，表明其耐腐蚀性能有所提高。腐蚀后表面分析显示，裸露钢表面存在较厚的硫化物和氧化物层，而在渗硼样品上观察到分散的腐蚀颗粒。硼化钢的磨损性能和电化学性能的提高主要是由于其表面的FeB/Fe2B层较硬，其表面吸附的硫量减少。
{"title":"Improving the Mechanical and Electrochemical Performance of Additively Manufactured 8620 Low Alloy Steel via Boriding","authors":"Ezazul Haque Sabuz, Mohammed Noor-A-Alam, Waseem Haider, Ishraq Shabib","doi":"10.3390/cmd4040032","DOIUrl":"https://doi.org/10.3390/cmd4040032","url":null,"abstract":"In this study, mechanical and electrochemical performance of borided additively manufactured (AM) and wrought 8620 low alloy steel were investigated and compared to their bare counterparts. The microstructure of borided 8620 exhibited the presence of FeB and Fe2B phases with a saw tooth morphology. Both AM and wrought samples with boride layers showed a similar performance in hardness, wear, potentiodynamic polarization (PD), electrochemical impedance spectroscopy (EIS), and linear polarization resistance (LPR) experiments. However, borided steels exhibited about an 8-fold increase in Vickers hardness and about a 6-fold enhancement in wear resistance compared to bare ones. Electrochemical experiments of borided specimens (both AM and wrought) in 0.1 M Na2S2O3 + 1 M NH4Cl solution revealed a 3–6-fold lower corrosion current density, about a 6-fold higher charge transfer resistance, and about a 6-fold lower double-layer capacitance, demonstrating an improved corrosion resistance compared to their bare counterparts. Post-corrosion surface analysis revealed the presence of thick sulfide and oxide layers on the bare steels, whereas dispersed corrosion particles were observed on the borided samples. The enhanced wear and electrochemical performance of the borided steels were attributed to the hard FeB/Fe2B layers and the reduced amount of adsorbed sulfur on their surface.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"8 6","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135589857","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zhengyu Zhang, Raja Shekar Bhupal Dandu, Edwin Eyram Klu, Wenjun Cai
Tribocorrosion, a research field that has been evolving for decades, has gained renewed attention in recent years, driven by increased demand for wear- and corrosion-resistant materials from biomedical implants, nuclear power generation, advanced manufacturing, batteries, marine and offshore industries, etc. In the United States, wear and corrosion are estimated to cost nearly USD 300 billion per year. Among various important structural materials, passive metals such as aluminum alloys are most vulnerable to tribocorrosion due to the wear-accelerated corrosion as a result of passive film removal. Thus, designing aluminum alloys with better tribocorrosion performance is of both scientific and practical importance. This article reviews five decades of research on the tribocorrosion of aluminum alloys, from experimental to computational studies. Special focus is placed on two aspects: (1) The effects of alloying and grain size on the fundamental wear, corrosion, and tribocorrosion mechanisms; and (2) Alloy design strategies to improve the tribocorrosion resistance of aluminum alloys. Finally, the paper sheds light on the current challenges faced and outlines a few future research directions in the field of tribocorrosion of aluminum alloys.
{"title":"A Review on Tribocorrosion Behavior of Aluminum Alloys: From Fundamental Mechanisms to Alloy Design Strategies","authors":"Zhengyu Zhang, Raja Shekar Bhupal Dandu, Edwin Eyram Klu, Wenjun Cai","doi":"10.3390/cmd4040031","DOIUrl":"https://doi.org/10.3390/cmd4040031","url":null,"abstract":"Tribocorrosion, a research field that has been evolving for decades, has gained renewed attention in recent years, driven by increased demand for wear- and corrosion-resistant materials from biomedical implants, nuclear power generation, advanced manufacturing, batteries, marine and offshore industries, etc. In the United States, wear and corrosion are estimated to cost nearly USD 300 billion per year. Among various important structural materials, passive metals such as aluminum alloys are most vulnerable to tribocorrosion due to the wear-accelerated corrosion as a result of passive film removal. Thus, designing aluminum alloys with better tribocorrosion performance is of both scientific and practical importance. This article reviews five decades of research on the tribocorrosion of aluminum alloys, from experimental to computational studies. Special focus is placed on two aspects: (1) The effects of alloying and grain size on the fundamental wear, corrosion, and tribocorrosion mechanisms; and (2) Alloy design strategies to improve the tribocorrosion resistance of aluminum alloys. Finally, the paper sheds light on the current challenges faced and outlines a few future research directions in the field of tribocorrosion of aluminum alloys.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"34 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135889946","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Time series experiments were used to explore the fluid redox impact on the corrosion of Q125, 316L, and C276 steels in low-ionic-strength and neutral water at temperature and pressure conditions associated with low-temperature geothermal systems. After exposing polished samples of each steel grade to an oxidizing (H2O2) and a reducing (Zn-doped) fluid for intervals of 24 h, 1 week, and 6 weeks, the atomic force microscopy results revealed general corrosion for Q125, while 316L and C276 exhibited pitting, crevice expansion, and edge attack corrosion. Secondary depositional features are frequently found as topographic highs, adjacent to pitting corrosion. These features may be identified as there is a very strong spatial correlation between the height retrace and phase retrace surface maps. All steels became progressively rougher over time after exposure to both fluids, while the corrosion rates were more complex. Samples exposed to the reducing fluid experienced an increase in the corrosion rate over time, while C276 and 316L experienced a decrease in the corrosion rate. Finally, a novel data validation technique was developed to address the intrinsic scalability of corrosion. The results indicate that the AFM scan area does not affect the measured surface roughness over nearly three orders of magnitude.
{"title":"Evaluating the Impact of Redox Potential on the Corrosion of Q125, 316L, and C276 Steel in Low-Temperature Geothermal Systems","authors":"Samuel Bowman, Vikas Agrawal, Shikha Sharma","doi":"10.3390/cmd4040030","DOIUrl":"https://doi.org/10.3390/cmd4040030","url":null,"abstract":"Time series experiments were used to explore the fluid redox impact on the corrosion of Q125, 316L, and C276 steels in low-ionic-strength and neutral water at temperature and pressure conditions associated with low-temperature geothermal systems. After exposing polished samples of each steel grade to an oxidizing (H2O2) and a reducing (Zn-doped) fluid for intervals of 24 h, 1 week, and 6 weeks, the atomic force microscopy results revealed general corrosion for Q125, while 316L and C276 exhibited pitting, crevice expansion, and edge attack corrosion. Secondary depositional features are frequently found as topographic highs, adjacent to pitting corrosion. These features may be identified as there is a very strong spatial correlation between the height retrace and phase retrace surface maps. All steels became progressively rougher over time after exposure to both fluids, while the corrosion rates were more complex. Samples exposed to the reducing fluid experienced an increase in the corrosion rate over time, while C276 and 316L experienced a decrease in the corrosion rate. Finally, a novel data validation technique was developed to address the intrinsic scalability of corrosion. The results indicate that the AFM scan area does not affect the measured surface roughness over nearly three orders of magnitude.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"27 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135251580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
As a result of the exponential growth in the production of plastics and their extended degradation period, strong environmental concerns in association with the disposal of plastic waste have emerged. Pursuing sustainable solutions for managing plastic waste has led to significant interest in plastic biodegradation research, with a specific focus on biodeterioration facilitated by microorganisms. The biodeterioration of plastic by microorganisms is a complex phenomenon that can be influenced by a variety of environmental factors such as humidity, temperature, and pH, as well as polymer properties such as molecular structure, molecular weight, and crystallinity. Toward a better understanding of this phenomenon for resolving the issue of plastic waste, this review article focuses on the biodeterioration of synthetic polymers, in particular aliphatic polyesters and polyolefins, through the enzymatic activities of microorganisms. First, the mechanism of polymer biodegradation via enzymatic activity is discussed, followed by the physical properties of polymers and environmental conditions that influence their biodegradability rates. Then, an overview of experimental approaches and standardized protocols used to assess the biodegradability of polymers by these degrading agents is provided. Finally, current developments in employing biodeterioration for the degradation of aliphatic polyesters and polyolefins are reviewed. The review concludes with a discussion on the complexity of biodegradation by microorganisms, the necessity of proper engineering of polymer properties during production to enhance their biodegradability, and the need for further research to discover sustainable and environmentally acceptable alternatives.
{"title":"State-of-the-Art Review of Aliphatic Polyesters and Polyolefins Biodeterioration by Microorganisms: From Mechanism to Characterization","authors":"Shiva Khoshtinat","doi":"10.3390/cmd4040029","DOIUrl":"https://doi.org/10.3390/cmd4040029","url":null,"abstract":"As a result of the exponential growth in the production of plastics and their extended degradation period, strong environmental concerns in association with the disposal of plastic waste have emerged. Pursuing sustainable solutions for managing plastic waste has led to significant interest in plastic biodegradation research, with a specific focus on biodeterioration facilitated by microorganisms. The biodeterioration of plastic by microorganisms is a complex phenomenon that can be influenced by a variety of environmental factors such as humidity, temperature, and pH, as well as polymer properties such as molecular structure, molecular weight, and crystallinity. Toward a better understanding of this phenomenon for resolving the issue of plastic waste, this review article focuses on the biodeterioration of synthetic polymers, in particular aliphatic polyesters and polyolefins, through the enzymatic activities of microorganisms. First, the mechanism of polymer biodegradation via enzymatic activity is discussed, followed by the physical properties of polymers and environmental conditions that influence their biodegradability rates. Then, an overview of experimental approaches and standardized protocols used to assess the biodegradability of polymers by these degrading agents is provided. Finally, current developments in employing biodeterioration for the degradation of aliphatic polyesters and polyolefins are reviewed. The review concludes with a discussion on the complexity of biodegradation by microorganisms, the necessity of proper engineering of polymer properties during production to enhance their biodegradability, and the need for further research to discover sustainable and environmentally acceptable alternatives.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"73 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135591384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A conventionally cast CoNiFeMn0.5Cr1.5 alloy and two versions with 0.25 C & 3.7 Ta or 0.25 C & 3.7 Hf were tested in oxidation at 1000 °C for 50 h with thermogravimetric recording of the oxidation kinetic. In all cases, the obtained mass gain curve is parabolic. The parabolic constants are much lower than the Kp previously determined for the original alloys with an equimolar base (CoNiFeMnCr). However, the post-mortem exploitation of the oxidized samples revealed analogous oxidation features on the surface and the subsurface, also with external oxide strata on the surface with different Mn and Cr contents, and rather great Mn depletion, in addition to a moderate Cr depletion, in the subsurface. Globally, the oxidation behavior is significantly better than was earlier observed for the equimolar version of these alloys.
常规铸造CoNiFeMn0.5Cr1.5合金和两个0.25 C &的版本;3.7 Ta或0.25 C &3.7在1000℃下氧化50 h，用热重法记录氧化动力学。在所有情况下，得到的质量增益曲线都是抛物线。抛物线常数远低于先前测定的等摩尔碱(CoNiFeMnCr)原始合金的Kp。然而，对氧化样品的尸检发现，表面和地下都有类似的氧化特征，表面也有不同Mn和Cr含量的外部氧化层，除了地下有适度的Cr损耗外，地下还有相当大的Mn损耗。总体而言，这些合金的氧化行为明显优于之前观察到的等摩尔版本。
{"title":"Oxidation Behavior at 1000 °C of Low-Mn High-Cr Cantor’s HEA-Based Alloys Strengthened or Not by MC Carbides","authors":"Pauline Spaeter, Corentin Gay, Nassima Chenikha, Ghouti Medjahdi, Anne Vernière, Christophe Rapin, Lionel Aranda, Patrice Berthod","doi":"10.3390/cmd4040028","DOIUrl":"https://doi.org/10.3390/cmd4040028","url":null,"abstract":"A conventionally cast CoNiFeMn0.5Cr1.5 alloy and two versions with 0.25 C & 3.7 Ta or 0.25 C & 3.7 Hf were tested in oxidation at 1000 °C for 50 h with thermogravimetric recording of the oxidation kinetic. In all cases, the obtained mass gain curve is parabolic. The parabolic constants are much lower than the Kp previously determined for the original alloys with an equimolar base (CoNiFeMnCr). However, the post-mortem exploitation of the oxidized samples revealed analogous oxidation features on the surface and the subsurface, also with external oxide strata on the surface with different Mn and Cr contents, and rather great Mn depletion, in addition to a moderate Cr depletion, in the subsurface. Globally, the oxidation behavior is significantly better than was earlier observed for the equimolar version of these alloys.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"59 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135863324","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rin Takada, Kota Hirasawa, Hideaki Takahashi, Makoto Chiba
Recently, new surface treatments for the corrosion protection of Al alloys by forming self-healing layers have attracted the attention of many researchers. The authors of this paper have previously developed self-healing polyurethane coatings with micro-capsules containing healing agents and porous anodic oxide films filled with healing agents. In this study, self-healing coatings consisting of an outer electrodeposited epoxy resin layer and an inner porous anodic oxide layer with healing agents were developed for the corrosion protection of Al alloys. The corrosion protection abilities of the self-healing coating were shown in Cu2+/Cl− solutions after damaging with indenters and were affected by freezing treatments and the tip angles of the indenter.
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