Promotion of Plant Growth in Arid Zones by Selected Trichoderma spp. Strains with Adaptation Plasticity to Alkaline pH

Trichoderma species are filamentous fungi that support plant health and confer improved growth, disease resistance, and abiotic stress tolerance. The objective of this study is to describe the physiological characteristics of the abundance and structure of Trichoderma model strains from arid zones and evaluate and describe their possible adaptation and modulation in alkaline pH. The presence of biotic factors such as phytopathogens forces farmers to take more actions such as using pesticides. In addition, factors such as the lack of water worldwide lead to losses in agricultural production. Therefore, the search for biocontrol microorganisms that support drought opens the door to the search for variations in the molecular mechanisms involved in these phenomena. In our case, we isolated 11 tested Trichoderma fungal strains from samples collected both from the rhizosphere and roots from two endemic plants. We probed their molecular markers to obtain their identity and assessed their resistance to alkaline conditions, as well as their response to mycoparasitism, plant growth promotion, and drought stress. The findings were worthy of being analyzed in depth. Three fungal taxa/species were grouped by phylogenetic/phenotypic characteristics; three T. harzianum strains showed outstanding capabilities to adapt to alkalinity stress. They also showed antagonistic activity against three phytopathogenic fungi. Additionally, we provided evidence of significant growth promotion in Sorghum bicolor seedlings under endemic agriculture conditions and a reduction in drought damage with Trichoderma infection. Finally, beneficial fungi adapted to specific ambient niches use various molecular mechanisms to survive and modulate their metabolism

Electrochemical Corrosion of Titanium and Titanium Alloys Anodized in H2SO4 and H3PO4 Solutions

Titanium and its alloys have superior electrochemical properties compared to other alloy systems due to the formation of a protective TiO2 film on metal surfaces. The ability to generate the protective oxide layer will depend upon the type of alloy to be used. The aim of this work was to characterize the electrochemical corrosion behavior of titanium Ti-CP2 and alloys Ti-6Al-2Sn-4Zr-2Mo, Ti-6Al-4V, and Ti Beta-C. Samples were anodized in 1 M H2SO4 and H3PO4 solutions with a current density of 0.025 A/cm2. Electrochemical tests on anodized alloys were carried out using a three-electrode cell and exposed in two electrolytes, i.e., 3.5 wt % NaCl and 3.5 wt % H2SO4 solutions at room temperature. Scanning electron microscopy (SEM) was used to observe the morphology of anodized surfaces. The electrochemical techniques used were cyclic potentiodynamic polarization (CPP) and electrochemical noise (EN), based on the ASTM-G61 and G199 standards. Regarding EN, two methods of data analysis were used: the frequency domain (power spectral density, PSD) and time-frequency domain (discrete wavelet transform). For non-anodized alloys, the results by CCP and EN indicate icorr values of ×10−6 A/cm2. However, under anodizing conditions, the icorr values vary from ×10−7 to ×10−9 A/cm2. The PSD Ψ0 values are higher for non-anodized alloys, while in anodized conditions, the values range from −138/−122 dBi (A2·Hz−1)1/2 to −131/−180 dBi (A2·Hz−1)1/2. Furthermore, the results indicated that the alloys anodized in the H3PO4 bath showed an electrochemical behavior that can be associated with a more homogeneous passive layer when exposed to the 3.5 wt % NaCl electrolyte. Alloys containing more beta-phase stabilizers formed a less homogeneous anodized layer. These alloys are widely used in aeronautical applications; thus, it is essential that these alloys have excellent corrosion performance in chloride and acid rain environments

A Comparative Study of Corrosion AA6061 and AlSi10Mg Alloys Produced by Extruded and Additive Manufacturing

The aim of this work was to evaluate the corrosion behavior of the AA6061 and AlSi10Mg alloys produced by extruded and additive manufacturing (selective laser melting, SLM). Alloys were immersed in two electrolytes in H2O and 3.5 wt. % NaCl solutions at room temperature and their corrosion behavior was studied by electrochemical noise technique (EN). Three different methods filtered EN signals, and the statistical analysis was employed to obtain Rn, the localization index (LI), Kurtosis, skew, and the potential spectral density analysis (PSD). The Energy Dispersion Plots (EDP) of wavelets method was employed to determine the type of corrosion and the Hilbert–Huang Transform (HHT), analyzing the Hilbert Spectra. The result indicated that the amplitude of the transients in the time series in potential and current is greater in the AlSi10Mg alloy manufactured by additive manufacturing. The amplitude of the transients decreases in both alloys (AA6061 and AlSi10Mg) as time increases

Electrochemical Corrosion of Titanium and Titanium Alloys Anodized in H2SO4 and H3PO4 Solutions

Titanium and its alloys have superior electrochemical properties compared to other alloy systems due to the formation of a protective TiO2 film on metal surfaces. The ability to generate the protective oxide layer will depend upon the type of alloy to be used. The aim of this work was to characterize the electrochemical corrosion behavior of titanium Ti-CP2 and alloys Ti-6Al-2Sn 4Zr-2Mo, Ti-6Al-4V, and Ti Beta-C. Samples were anodized in 1 M H2SO4 and H3PO4 solutions with a current density of 0.025 A/cm2 . Electrochemical tests on anodized alloys were carried out using a three-electrode cell and exposed in two electrolytes, i.e., 3.5 wt % NaCl and 3.5 wt % H2SO4 solutions at room temperature. Scanning electron microscopy (SEM) was used to observe the morphology of anodized surfaces. The electrochemical techniques used were cyclic potentiodynamic polarization (CPP) and electrochemical noise (EN), based on the ASTM-G61 and G199 standards. Regarding EN, two methods of data analysis were used: the frequency domain (power spectral density, PSD) and time-frequency domain (discrete wavelet transform). For non-anodized alloys, the results by CCP and EN indicate icorr values of ×10−6 A/cm2 . However, under anodizing conditions, the icorr values vary from ×10−7 to ×10−9 A/cm2 . The PSD Ψ0 values are higher for non anodized alloys, while in anodized conditions, the values range from −138/−122 dBi (A2 ·Hz−1 ) 1/2 to −131/−180 dBi (A2 ·Hz−1 ) 1/2. Furthermore, the results indicated that the alloys anodized in the H3PO4 bath showed an electrochemical behavior that can be associated with a more homogeneous passive layer when exposed to the 3.5 wt % NaCl electrolyte. Alloys containing more beta-phase stabilizers formed a less homogeneous anodized layer. These alloys are widely used in aeronautical applications; thus, it is essential that these alloys have excellent corrosion performance in chloride and acid rain environments

Electrochemical Noise Analysis of the Corrosion of Titanium Alloys in NaCl and H2SO4 Solutions

Titanium alloys have been used in aerospace, aeronautic, automotive, biomedical, structural, and other applications because titanium alloys have less density than materials like steel and support higher stress than Al-alloys. However, components made of titanium alloys are exposed to corrosive environments, the most common being industrial and marine atmospheres. This research shows the corrosion behavior of three titanium alloys, specifically Ti-CP2, Ti-6Al-2Sn-4Zr-2Mo, and Ti-6Al-4V with α, near α, and α + β alloys phases. Alloys were exposed in two electrolytes to a 3.5 wt. % H2SO4 and NaCl solution at room temperature, and their electrochemical behavior was studied by electrochemical noise technique (EN) according to ASTM ASTM-G199 standard. EN signal was filtered by three different methods, and the polynomial method was employed to obtain Rn, kurtosis, skew, and the potential spectral density analysis (PSD). The wavelets method was used, from which energy dispersion plots were obtained. The last method was Hilbert–Huang Transform (HHT), where Hilbert Spectra were analyzed. Results indicated that Rn compared with PSD showed that Ti-6Al-2Sn-4Zr-2Mo presented less dissolution in both electrolytes. Statistical methods showed that the passive layer created on Ti alloys’ surfaces is unstable; this condition is notable for Ti-6Al-2Sn-4Zr-2Mo in NaCl solution

A Comparative Study of Corrosion AA6061 and AlSi10Mg Alloys Produced by Extruded and Additive Manufacturing

The aim of this work was to evaluate the corrosion behavior of the AA6061 and AlSi10Mg alloys produced by extruded and additive manufacturing (selective laser melting, SLM). Alloys were immersed in two electrolytes in H2O and 3.5 wt. % NaCl solutions at room temperature and their corrosion behavior was studied by electrochemical noise technique (EN). Three different methods filtered EN signals, and the statistical analysis was employed to obtain Rn, the localization index (LI), Kurtosis, skew, and the potential spectral density analysis (PSD). The Energy Dispersion Plots (EDP) of wavelets method was employed to determine the type of corrosion and the Hilbert–Huang Transform (HHT), analyzing the Hilbert Spectra. The result indicated that the amplitude of the transients in the time series in potential and current is greater in the AlSi10Mg alloy manufactured by additive manufacturing. The amplitude of the transients decreases in both alloys (AA6061 and AlSi10Mg) as time increases

Electrochemical Corrosion of Titanium and Titanium Alloys Anodized in H2SO4 and H3PO4 Solutions

Titanium and its alloys have superior electrochemical properties compared to other alloy systems due to the formation of a protective TiO2 film on metal surfaces. The ability to generate the protective oxide layer will depend upon the type of alloy to be used. The aim of this work was to characterize the electrochemical corrosion behavior of titanium Ti-CP2 and alloys Ti-6Al-2Sn-4Zr-2Mo, Ti-6Al-4V, and Ti Beta-C. Samples were anodized in 1 M H2SO4 and H3PO4 solutions with a current density of 0.025 A/cm2. Electrochemical tests on anodized alloys were carried out using a three-electrode cell and exposed in two electrolytes, i.e., 3.5 wt % NaCl and 3.5 wt % H2SO4 solutions at room temperature. Scanning electron microscopy (SEM) was used to observe the morphology of anodized surfaces. The electrochemical techniques used were cyclic potentiodynamic polarization (CPP) and electrochemical noise (EN), based on the ASTM-G61 and G199 standards. Regarding EN, two methods of data analysis were used: the frequency domain (power spectral density, PSD) and time-frequency domain (discrete wavelet transform). For non-anodized alloys, the results by CCP and EN indicate icorr values of ×10−6 A/cm2. However, under anodizing conditions, the icorr values vary from ×10−7 to ×10−9 A/cm2. The PSD Ψ0 values are higher for non-anodized alloys, while in anodized conditions, the values range from −138/−122 dBi (A2·Hz−1)1/2 to −131/−180 dBi (A2·Hz−1)1/2. Furthermore, the results indicated that the alloys anodized in the H3PO4 bath showed an electrochemical behavior that can be associated with a more homogeneous passive layer when exposed to the 3.5 wt % NaCl electrolyte. Alloys containing more beta-phase stabilizers formed a less homogeneous anodized layer. These alloys are widely used in aeronautical applications; thus, it is essential that these alloys have excellent corrosion performance in chloride and acid rain environment

Corrosion Behavior of Passivated Martensitic and Semi-Austenitic Precipitation Hardening Stainless Steel

This research aimed to conduct a passive layer state study on martensitic and semi-austenitic precipitation hardening stainless steels (PHSS) passivated in citric acid and nitric acid baths at 49 and 70 °C for 50 and 75 min and subsequently exposed in 5 wt.% NaCl and 1 wt.% H2SO4 solutions. Corrosion behavior of the passivated material was observed by using potentiodynamic polarization (PP) according to the ASTM G5-11 standard. The microstructural analysis was performed by optical microscopy and scanning electron microscopy (SEM), while the passivated layer was characterized by X-ray photoelectron spectroscopy (XPS). The results indicated that the semi-austenitic-NA-50 min-70 °C sample showed the best corrosion resistance behavior in both solutions. The XPS characterization confirmed that the martensitic and semi-austenitic surface film presented a mixture of chemical compounds, such as Cr2O3 and Fe(OH)O, respectively