Chitosan-Based Green and Sustainable Corrosion Inhibitors for Carbon Steel

Development of non-toxic and environmental friendly corrosion inhibitors is highly desirable owing to the increasing demands of “green chemistry” throughout the world. In view of these several forms of green corrosion inhibitors such as drugs or medicines, plant extracts, ionic liquids and synthetic inhibitors derived from multicomponent reactions (MCRs) and mechanochemical mixing are being employed. Nowadays, MCRs in association with microwave and ultrasound irradiations represent one of the best green strategies. Natural polysaccharides particularly chitosan derivatives gained substantial advancement. Chitosan and its several derivatives have been employed effective as corrosion inhibitors for metals and alloys in various aggressive media. The present chapter features the collection of major works that have been published on the inhibition effect of chitosan and its derivatives. The utilization of the chitosan and its derivatives as effective corrosion inhibitors is based on the fact that they contain several polar functional groups such as amino (-NH2), hydroxyl (-OH) and acetyl (-COCH3) groups that effectively bind with metallic surface and behave as adsorption centers

Global burden of 288 causes of death and life expectancy decomposition in 204 countries and territories and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021

BACKGROUND Regular, detailed reporting on population health by underlying cause of death is fundamental for public health decision making. Cause-specific estimates of mortality and the subsequent effects on life expectancy worldwide are valuable metrics to gauge progress in reducing mortality rates. These estimates are particularly important following large-scale mortality spikes, such as the COVID-19 pandemic. When systematically analysed, mortality rates and life expectancy allow comparisons of the consequences of causes of death globally and over time, providing a nuanced understanding of the effect of these causes on global populations. METHODS The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 cause-of-death analysis estimated mortality and years of life lost (YLLs) from 288 causes of death by age-sex-location-year in 204 countries and territories and 811 subnational locations for each year from 1990 until 2021. The analysis used 56 604 data sources, including data from vital registration and verbal autopsy as well as surveys, censuses, surveillance systems, and cancer registries, among others. As with previous GBD rounds, cause-specific death rates for most causes were estimated using the Cause of Death Ensemble model-a modelling tool developed for GBD to assess the out-of-sample predictive validity of different statistical models and covariate permutations and combine those results to produce cause-specific mortality estimates-with alternative strategies adapted to model causes with insufficient data, substantial changes in reporting over the study period, or unusual epidemiology. YLLs were computed as the product of the number of deaths for each cause-age-sex-location-year and the standard life expectancy at each age. As part of the modelling process, uncertainty intervals (UIs) were generated using the 2·5th and 97·5th percentiles from a 1000-draw distribution for each metric. We decomposed life expectancy by cause of death, location, and year to show cause-specific effects on life expectancy from 1990 to 2021. We also used the coefficient of variation and the fraction of population affected by 90% of deaths to highlight concentrations of mortality. Findings are reported in counts and age-standardised rates. Methodological improvements for cause-of-death estimates in GBD 2021 include the expansion of under-5-years age group to include four new age groups, enhanced methods to account for stochastic variation of sparse data, and the inclusion of COVID-19 and other pandemic-related mortality-which includes excess mortality associated with the pandemic, excluding COVID-19, lower respiratory infections, measles, malaria, and pertussis. For this analysis, 199 new country-years of vital registration cause-of-death data, 5 country-years of surveillance data, 21 country-years of verbal autopsy data, and 94 country-years of other data types were added to those used in previous GBD rounds. FINDINGS The leading causes of age-standardised deaths globally were the same in 2019 as they were in 1990; in descending order, these were, ischaemic heart disease, stroke, chronic obstructive pulmonary disease, and lower respiratory infections. In 2021, however, COVID-19 replaced stroke as the second-leading age-standardised cause of death, with 94·0 deaths (95% UI 89·2-100·0) per 100 000 population. The COVID-19 pandemic shifted the rankings of the leading five causes, lowering stroke to the third-leading and chronic obstructive pulmonary disease to the fourth-leading position. In 2021, the highest age-standardised death rates from COVID-19 occurred in sub-Saharan Africa (271·0 deaths [250·1-290·7] per 100 000 population) and Latin America and the Caribbean (195·4 deaths [182·1-211·4] per 100 000 population). The lowest age-standardised death rates from COVID-19 were in the high-income super-region (48·1 deaths [47·4-48·8] per 100 000 population) and southeast Asia, east Asia, and Oceania (23·2 deaths [16·3-37·2] per 100 000 population). Globally, life expectancy steadily improved between 1990 and 2019 for 18 of the 22 investigated causes. Decomposition of global and regional life expectancy showed the positive effect that reductions in deaths from enteric infections, lower respiratory infections, stroke, and neonatal deaths, among others have contributed to improved survival over the study period. However, a net reduction of 1·6 years occurred in global life expectancy between 2019 and 2021, primarily due to increased death rates from COVID-19 and other pandemic-related mortality. Life expectancy was highly variable between super-regions over the study period, with southeast Asia, east Asia, and Oceania gaining 8·3 years (6·7-9·9) overall, while having the smallest reduction in life expectancy due to COVID-19 (0·4 years). The largest reduction in life expectancy due to COVID-19 occurred in Latin America and the Caribbean (3·6 years). Additionally, 53 of the 288 causes of death were highly concentrated in locations with less than 50% of the global population as of 2021, and these causes of death became progressively more concentrated since 1990, when only 44 causes showed this pattern. The concentration phenomenon is discussed heuristically with respect to enteric and lower respiratory infections, malaria, HIV/AIDS, neonatal disorders, tuberculosis, and measles. INTERPRETATION Long-standing gains in life expectancy and reductions in many of the leading causes of death have been disrupted by the COVID-19 pandemic, the adverse effects of which were spread unevenly among populations. Despite the pandemic, there has been continued progress in combatting several notable causes of death, leading to improved global life expectancy over the study period. Each of the seven GBD super-regions showed an overall improvement from 1990 and 2021, obscuring the negative effect in the years of the pandemic. Additionally, our findings regarding regional variation in causes of death driving increases in life expectancy hold clear policy utility. Analyses of shifting mortality trends reveal that several causes, once widespread globally, are now increasingly concentrated geographically. These changes in mortality concentration, alongside further investigation of changing risks, interventions, and relevant policy, present an important opportunity to deepen our understanding of mortality-reduction strategies. Examining patterns in mortality concentration might reveal areas where successful public health interventions have been implemented. Translating these successes to locations where certain causes of death remain entrenched can inform policies that work to improve life expectancy for people everywhere. FUNDING Bill & Melinda Gates Foundation

In Vitro Corrosion and Bioactivity Performance of Surface-Treated Ti-20Nb-13Zr Alloys for Orthopedic Applications

The influence of surface treatments on the microstructure, in vitro bioactivity and corrosion protection performance of newly fabricated Ti-20Nb-13Zr (TNZ) alloys was evaluated in simulated body fluid (SBF). The TNZ alloy specimens were treated with separate aqueous solutions of NaOH and H2O2 and with a mixture of both, followed by thermal treatment. The nanoporous network surface structure observed in H2O2-treated and alkali-treated specimens was entirely different from the rod-like morphology observed in alkali hydrogen peroxide-treated specimens. XRD results revealed the formation of TiO2 and sodium titanate layers on the TNZ specimens during surface treatments. The water contact angle results implied that the surface-treated specimens exhibited improved surface hydrophilicity, which probably improved the bioactivity of the TNZ specimens. The in vitro corrosion protection performance of the surface-treated TNZ specimens was analyzed using electrochemical corrosion testing in SBF, and the obtained results indicated that the surface-treated specimens exhibited improved corrosion resistance performance compared to that of the bare TNZ specimen. The in vitro bioactivity of the treated TNZ specimens was assessed by soaking in SBF, and all the investigated treated specimens showed numerous apatite nucleation spheres within 3 days of immersion in SBF

In Vitro Corrosion and Bioactivity Performance of Surface-Treated Ti-20Nb-13Zr Alloys for Orthopedic Applications

The influence of surface treatments on the microstructure, in vitro bioactivity and corrosion protection performance of newly fabricated Ti-20Nb-13Zr (TNZ) alloys was evaluated in simulated body fluid (SBF). The TNZ alloy specimens were treated with separate aqueous solutions of NaOH and H2O2 and with a mixture of both, followed by thermal treatment. The nanoporous network surface structure observed in H2O2-treated and alkali-treated specimens was entirely different from the rod-like morphology observed in alkali hydrogen peroxide-treated specimens. XRD results revealed the formation of TiO2 and sodium titanate layers on the TNZ specimens during surface treatments. The water contact angle results implied that the surface-treated specimens exhibited improved surface hydrophilicity, which probably improved the bioactivity of the TNZ specimens. The in vitro corrosion protection performance of the surface-treated TNZ specimens was analyzed using electrochemical corrosion testing in SBF, and the obtained results indicated that the surface-treated specimens exhibited improved corrosion resistance performance compared to that of the bare TNZ specimen. The in vitro bioactivity of the treated TNZ specimens was assessed by soaking in SBF, and all the investigated treated specimens showed numerous apatite nucleation spheres within 3 days of immersion in SBF

Surface Properties and In Vitro Corrosion Studies of Blasted and Thermally Treated Ti6Al4V Alloy for Bioimplant Applications

The biomedical Ti6Al4V alloy was thermally treated under sandblasting and mirror finish surface preparation conditions. The surface morphology, structure, roughness, wettability, and energy were characterized. Microhardness and in vitro corrosion studies were carried out. X-ray diffraction results showed a formation of rutile TiO2 phase for thermally treated samples under different pretreated conditions. The thermally oxidized samples exhibited an increase in microhardness compared to the untreated mirror finish and sandblasted samples by 22 and 33%, respectively. The wettability study revealed enhanced hydrophilicity of blasted and thermally treated samples. The surface energy of the thermal treatment samples increased by 26 and 32.6% for mirror surface and blasted preconditions, respectively. The acquired in vitro corrosion results using potentiodynamic polarization measurement and electrochemical impedance spectroscopy confirmed the surface protective performance against corrosion in Hank’s medium. The enhanced surface characteristics and corrosion protection of treated Ti6Al4V alloy give it potential for bio-implant applications

Hybrid Polyurethane/Polypyrrole Composite Coatings on Passivated 316L SS for Surface Protective Action against Corrosion in Saline Medium

Hybrid treatments consisting of surface modification and subsequent protective coatings have gained extensive attention among corrosion mitigation approaches for a wide variety of structural metallic materials. This study aims to review the enhancement of the corrosion protection performance of polyurethane (PU) coatings on 316L stainless steel (SS) specimens. This was achieved via a two-step strategic treatment, primarily by electrochemical passivation and subsequent deposition of PU composite coatings with the different feed ratio of synthesized polypyrrole (PPy) nanoparticles. The effect of different applied voltage on the surface features and the corrosion behavior of the passivated SS surfaces was systematically investigated using surface characterization techniques and a potentiodynamic polarization test in a NaCl solution. Surface morphological images revealed the porous structure on the passivated surface. It is inferred from the topographical surface results that homogeneous surface roughness was achieved with the applied voltage of 5 V. Infra-red spectroscopic results validate the formation of PU/PPy composite coatings and the intermolecular chemical interaction between the PU and PPy moieties. Furthermore, corrosion measurements corroborate the improved corrosion resistance of PU/30PPy coatings with higher values of charge transfer resistance, Rct (1.0869 × 107 Ω cm2), and film resistance, Rf (2.258 × 105 Ω cm2), with the lowest values of corrosion, icorr (4.7 × 10−3 µA cm−2) compared to that of the PU/Bare specimen. In conclusion, it is confirmed that the passivated surface enhances the corrosion resistance performance of PU coated SS, and this performance is further increased with the incorporation of PPy particles

Hybrid Polyurethane/Polypyrrole Composite Coatings on Passivated 316L SS for Surface Protective Action against Corrosion in Saline Medium

Hybrid treatments consisting of surface modification and subsequent protective coatings have gained extensive attention among corrosion mitigation approaches for a wide variety of structural metallic materials. This study aims to review the enhancement of the corrosion protection performance of polyurethane (PU) coatings on 316L stainless steel (SS) specimens. This was achieved via a two-step strategic treatment, primarily by electrochemical passivation and subsequent deposition of PU composite coatings with the different feed ratio of synthesized polypyrrole (PPy) nanoparticles. The effect of different applied voltage on the surface features and the corrosion behavior of the passivated SS surfaces was systematically investigated using surface characterization techniques and a potentiodynamic polarization test in a NaCl solution. Surface morphological images revealed the porous structure on the passivated surface. It is inferred from the topographical surface results that homogeneous surface roughness was achieved with the applied voltage of 5 V. Infra-red spectroscopic results validate the formation of PU/PPy composite coatings and the intermolecular chemical interaction between the PU and PPy moieties. Furthermore, corrosion measurements corroborate the improved corrosion resistance of PU/30PPy coatings with higher values of charge transfer resistance, Rct (1.0869 × 107 Ω cm2), and film resistance, Rf (2.258 × 105 Ω cm2), with the lowest values of corrosion, icorr (4.7 × 10−3 µA cm−2) compared to that of the PU/Bare specimen. In conclusion, it is confirmed that the passivated surface enhances the corrosion resistance performance of PU coated SS, and this performance is further increased with the incorporation of PPy particles

Anticorrosion Properties of a Novel Hybrid Sol–Gel Coating on Aluminum 3003 Alloy

In this study, a novel hybrid sol–gel coating on AA3003 substrate was developed and the effects of various waste material additives on the reinforcement of the sol–gel coating and the anticorrosion properties in the saline medium were investigated. Egg shell, crumb rubber, activated carbon obtained for pyrolysis of waste rubber tire, waste rubber tire, cement kiln dust, and ST100 additives were tested as reinforcement materials. The AFM characterization results of the coating formulations on AA3003 alloy revealed enhanced roughness values for the modified coatings as compared to the base coating. Similarly, no significant changes were detected in the Fourier transform infrared spectroscopy (FTIR) absorption peaks of the hybrid polymeric material upon loading it with the waste additives, while slight changes in the hydrophobic properties of the final modified coatings were observed as a result of the modification process. Electrochemical impedance spectroscopy (EIS) results revealed that the hybrid sol–gel coating had a promising potential for the protection of the AA3003 substrate against corrosion in the saline medium. However, the loaded additives negatively affected the corrosion resistance properties of the parent hybrid sol–gel coating. For instance, the egg shell additive had the least negative effect on the barrier properties, whereas the cured coating layer of the sample loaded with cement and clay additives showed some disintegration, inhomogeneity, and low barrier properties on the metal surface

Fabrication and Electrochemical Corrosion Behavior of PEO Coatings on Strip-Cast AZ31Mg Alloy in 3.5% NaCl Solution

The generation of compact plasma electrolytic oxidation (PEO) coatings with outstanding corrosion resistance is essential for the widespread application of Mg alloys. In the present investigation, PEO ceramic coatings formed at different silicate concentration and oxidation time on AZ31 Mg alloy were studied, and the resultant surface structures of the oxide films were observed using scanning electron microscopy (SEM) and atomic force microscopy (AFM) analysis. X-ray photoelectron spectroscopy and thin film-X-ray diffraction analysis of ceramic coatings showed that the surface coating is mainly composed of Mg₂SiO₄, and MgO with different amount based on oxidation time. Further, the potentiodynamic polarization and electrochemical impedance spectroscopic (EIS) measurements were used to characterize corrosion behavior of PEO coated substrates in 3.5% NaCl solution. The results revealed that PEO coatings processed with 0.2 M silicate showed better performance due to its dense and compact coating with fewer structural imperfections in comparison to others