Search

The corrosion performance of as-solidified Al-Pd alloys in HCl and NaOH aqueous solutions is investigated in this work. Four different alloys (Al88Pd12, Al77Pd23, Al72Pd28 and Al67Pd33, element concentrations are given in at.%) were prepared from high purity Al and Pd lumps by arc-melting in Ar. Subsequently, the alloy microstructure and phase occurrence were investigated by a combination of scanning electron microscopy and room-temperature powder X-ray diffraction. The assolidified Al-Pd alloys were found to consist of several single-phase microstructure constituents with various structures and chemical compositions, including structurally complex intermetallic phases. The polished surfaces of the Al-Pd alloys were subjected to electrochemical polarization in aqueous HCl and NaOH solutions (0.01 mol.dm-3) at 21±2°C. The corrosion experiments were conducted in a standard 3-electrode cell controlled by potentiostat. The corrosion potentials and corrosion current densities were determined by Tafel extrapolation of the experimental polarization curves. Phase dissolution has been observed on the alloy surfaces and some of the phases were preferentially corroded. The effects of the alloy microstructure and the phase occurrence are evaluated. The local nobility of individual intermetallic compounds is discussed. Finally, the conclusions for the alloys corrosion performance in acidic and basic solutions are provided.

Abstract: The originally as-cast Al55Ni30Pd15 alloy was investigated during continuous heating from room temperature to 600 °C and after annealing at 600 °C for respective 455, 2650, and 4050 h. In the investigation the synchrotron X-ray diffraction and the high-resolution scanning electron microscopy inclusive of the energy-dispersive X-ray spectroscopy were used. In all the investigated conditions β-(Ni,Pd)Al (Pm3m) and Al3(NiPd)2 (P3m1) phases were identified. After 2650 h of annealing the former phase was found to be separated into two isostructural modifications differing from one another in Pd- and Ni-contents. The annealing for 455 h contributed to the decrease of lattice parameters in the Al3NiPd phase compared to the original as-cast condition. [Copyright &y& Elsevier]

The utilization of biochar as a relatively efficient sorbent or stationary phase for the separation and preconcentration of a wide range of analytes represents an innovative approach in current sample pretreatment methods. Appropriate pre- and post-pyrolysis modification of the input precursor and pyrolysis product, respectively, allows targeted design of the physicochemical properties and sorption characteristics of the resulting sorbent. The present work deals with the preparation of pyrolysis materials based on unmodified cattail leaf biomass (BC) and its Mg-modified analogue (MgBC) by a slow pyrolysis process at 500 °C and a residence time of 1 h in a pyrolysis reactor. Physicochemical characterization of BC and MgBC carried out by pH, total C, N, surface size analysis (SSA), 13 C NMR, SEM-EDX and XRD confirmed significant morphological and mineralogical differences between the prepared sorbents. By performing sorption experiments using a model anionic analyte (As) and application of Langmuir isotherm, we found that the predicted maximum sorption capacity of MgBC for As is 13.5-fold higher than that of BC. The sorption process of As by both sorbents is best described by the Sips adsorption isotherm (R 2  ≥ 0.995) and a pseudo-n th order kinetic model (R 2  ≥ 0.997). The optimum pH for As sorption by BC and MgBC sorbents is in the interval 5-6. The presence of competitive phosphate anions (equimolar concentration of 1:1) in the solution significantly reduces the sorption capacity of MgBC for As by 40% for BC by 70%. The presence of Cl- ions showed no significant effect on the sorption capacity of Bc and MgBC for As. Both sorbents were best recovered using 0.1 mol/L NaOH solution when the desorption efficiency for both sorbents was more than 95%. The MgBC sorbent showed 35% retention of As from the real sample in the model SPE column at a flow rate of 0.12 mL/s. Based on the obtained knowledge, it is evident that biochar-based sorbent prepared from Mg-modified precursor represents an effective sorbent for anionic forms of analytes and opens the possibility of its use also in preconcentration and separation techniques., Competing Interests: Declarations Competing interests The authors declare no competing interests., (© 2024. The Author(s).)

The present work investigates the influence of isothermal annealing on the microstructure and oxidation behavior of nanocomposite coatings. AlTiSiN/TiSiN coatings with TiSiN adhesive layer were deposited onto a high-speed steel substrate via physical vapor deposition. The coatings were investigated in the as-deposited state as well as after annealing in air at 700, 800, 900 and 1000 °C, respectively. The microstructure and morphology of the coatings were observed using scanning electron microscopy and transmission electron microscopy. The chemical composition and presence of oxidation products were studied by energy-dispersive X-ray spectroscopy. The phase identification was performed by means of X-ray diffraction. In the microstructure of the as-deposited coating, the (Ti 1-x Al x )N particles were embedded in an amorphous Si 3 N 4 matrix. TiO 2 and SiO 2 were found at all annealing temperatures, and Al 2 O 3 was additionally identified at 1000 °C. It was found that, with increasing annealing temperature, the thickness of the oxide layer increased, and its morphology and chemical composition changed. At 700 and 800 °C, a Ti-Si-rich surface oxide layer was formed. At 900 and 1000 °C, an oxidized part of the coating was observed in addition to the surface oxide layer. Compared to the as-deposited sample, the oxidized samples exhibited considerably worse mechanical properties.

In the present work, the microstructure, phase constitution, and corrosion behavior of binary Sn-xZn alloys (x = 5, 9 and 15 wt.%) were investigated. The alloys were prepared by induction melting of Sn and Zn lumps in argon. After melting, the alloys were solidified to form cast cylinders. The Sn-9Zn alloy had a eutectic microstructure. The Sn-5Zn and Sn-15Zn alloys were composed of dendritic (Sn) or (Zn) and eutectic. The corrosion behavior of the Sn-Zn alloys was studied in aqueous HCl (1 wt.%) and NaCl (3.5 wt.%) solutions at room temperature. Corrosion potentials and corrosion rates in HCl were significantly higher compared to NaCl. The corrosion of the binary Sn-Zn alloys was found to take place by a galvanic mechanism. The chemical composition of the corrosion products formed on the Sn-Zn alloys changed with the Zn weight fraction. Alloys with a higher concentration of Zn (Sn-9Zn, Sn-15Zn) formed corrosion products rich in Zn. The Zn-rich corrosion products were prone to spallation. The corrosion rate in the HCl solution decreased with decreasing weight fraction of Zn. The Sn-5Zn alloy had the lowest corrosion rate. The corrosion resistance in HCl could be considerably improved by reducing the proportion of zinc in Sn-Zn alloys.

Biochars from wood chips (WC) and corn cobs (CC) were prepared by slow pyrolysis and used for sorption separation of erythrosine B (EB) and thioflavin T (TT) in batch experiments. Biochar-based adsorbents were extensively characterized using FTIR, XRD, SEM-EDX, and XPS techniques. The kinetics studies revealed that adsorption on external surfaces was the rate-limiting step for the removal of TT on both WC and CC biochar, while intraparticle diffusion was the rate-limiting step for the adsorption of EB. Maximal experimental adsorption capacities Q maxexp of TT reached 182 ± 5 (WC) and 45 ± 2 mg g -1 (CC), and EB 12.7 ± 0.9 (WC) and 1.5 ± 0.4 mg g -1 (CC), respectively, thereby indicating a higher affinity of biochars for TT. The adsorption mechanism was found to be associated with π-π interaction, hydrogen bonding, and pore filling. Application of the innovative dynamic approach based on fast-field-cycling NMR relaxometry indicates that variations in the retention of water-soluble dyes could be explained by distinct water dynamics in the porous structures of WC and CC. The obtained results suggest that studied biochars will be more effective in adsorbing of cationic than anionic dyes from contaminated effluents.

Complex metallic alloys (CMAs) are materials composed of structurally complex intermetallic phases (SCIPs). The SCIPs consist of large unit cells containing hundreds or even thousands of atoms. Well-defined atomic clusters are found in their structure, typically of icosahedral point group symmetry. In SCIPs, a long-range order is observed. Aluminum-based CMAs contain approximately 70 at.% Al. In this paper, the corrosion behavior of bulk Al-based CMAs is reviewed. The Al-TM alloys (TM = transition metal) have been sorted according to their chemical composition. The alloys tend to passivate because of high Al concentration. The Al-Cr alloys, for example, can form protective passive layers of considerable thickness in different electrolytes. In halide-containing solutions, however, the alloys are prone to pitting corrosion. The electrochemical activity of aluminum-transition metal SCIPs is primarily determined by electrode potential of the alloying element(s). Galvanic microcells form between different SCIPs which may further accelerate the localized corrosion attack. The electrochemical nobility of individual SCIPs increases with increasing concentration of noble elements. The SCIPs with electrochemically active elements tend to dissolve in contact with nobler particles. The SCIPs with noble metals are prone to selective de-alloying (de-aluminification) and their electrochemical activity may change over time as a result of de-alloying. The metal composition of the SCIPs has a primary influence on their corrosion properties. The structural complexity is secondary and becomes important when phases with similar chemical composition, but different crystal structure, come into close physical contact.

In this work, the high temperature oxidation behavior of Al 71 Co 29 and Al 76 Co 24 alloys (concentration in at.%) is presented. The alloys were prepared by controlled arc-melting of Co and Al granules in high purity argon. The as-solidified alloys were found to consist of several different phases, including structurally complex m-Al 13 Co 4 and Z-Al 3 Co phases. The high temperature oxidation behavior of the alloys was studied by simultaneous thermal analysis in flowing synthetic air at 773-1173 K. A protective Al 2 O 3 scale was formed on the sample surface. A parabolic rate law was observed. The rate constants of the alloys have been found between 1.63 × 10 -14 and 8.83 × 10 -12 g cm -4 s -1 . The experimental activation energies of oxidation are 90 and 123 kJ mol -1 for the Al 71 Co 29 and Al 76 Co 24 alloys, respectively. The oxidation mechanism of the Al-Co alloys is discussed and implications towards practical applications of these alloys at high temperatures are provided.

The microstructure, phase constitution, and corrosion performance of as-solidified Al 70 Pd 25 Co 5 and Al 74 Pd 12 Co 14 alloys (element concentrations in at.%) have been investigated in the present work. The alloys were prepared by arc-melting of Al, Pd, and Co lumps in argon. The Al 74 Pd 12 Co 14 alloy was composed of structurally complex ε n phase, while the Al 70 Pd 25 Co 5 alloy was composed of ε n and δ phases. The corrosion performance was studied by open circuit potential measurements and potentiodynamic polarization in aqueous NaCl solution (3.5 wt.%). Marked open circuit potential oscillations of the Al 70 Pd 25 Co 5 alloy have been observed, indicating individual breakdown and re-passivation events on the sample surface. A preferential corrosion attack of ε n was found, while the binary δ phase (Al 3 Pd 2 ) remained free of corrosion. A de-alloying of Al from ε n and formation of intermittent interpenetrating channel networks occurred in both alloys. The corrosion behavior of ε n is discussed in terms of its chemical composition and crystal structure. The corrosion activity of ε n could be further exploited in preparation of porous Pd-Co networks with possible catalytic activity.