Ion-beam induced compositional and structural changes of Al-Cu-Co multilayer stacks

The present work deals with the investigation of ion-beam assisted annealing/mixing effects on compositional and structural changes in Al-Cu-Co multilayers. 800 nm thick Al64Cu20Co16 multilayers prepared by magnetron sputtering deposition, consisting of 28 successive single-metal Al-, Cu-, and Co-nanolayers were treated by thermal annealing at 300 °C, 400 °C, or 500 °C as well as ion irradiation by 30 MeV Cu5+ ions at fluences of 1x1013 to 5x1014 with an average flux of 2.38 × 1010 at.cm−2s−1. The samples were characterized with SEM, EDX, XRD, and TEM including HAADF. In contrast to the original multilayer, the treated samples were found to consist of two types of alternating nanolayers. A wider coarse-grained structurally and chemically homogeneous single-phase nanolayer formed by Al2Cu, and a narrow fine-grained two-phase nanolayer, which has a heterogeneous composite structure in which the central Co sublayer (being a residue of the original single-metal Co nanolayer) is surrounded from both sides with Al-Co sublayers, consisting of Al9Co2. This Co sublayer is considered to be a diffusion blocker for Al and Cu as well as hindering the movement of borders between particular nanolayers. The formation of a ternary phase in the investigated samples was not confirmed in any of the samples

Biochar from Wood Chips and Corn Cobs for Adsorption of Thioflavin T and Erythrosine B

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 pi-pi 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

Aqueous Corrosion of Aluminum-Transition Metal Alloys Composed of Structurally Complex Phases: A Review

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

Microstructure and Corrosion Behavior of Sn–Zn Alloys

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

Oxidation of Al-Co alloys at high temperatures

In this work, the high temperature oxidation behavior of Al71Co29 and Al76Co24 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-Al13Co4 and Z-Al3Co 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 Al2O3 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 Al71Co29 and Al76Co24 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

Relationship between Phase Occurrence, Chemical Composition, and Corrosion Behavior of as-Solidified Al–Pd–Co Alloys

The microstructure, phase constitution, and corrosion performance of as-solidified Al70Pd25Co5 and Al74Pd12Co14 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 Al74Pd12Co14 alloy was composed of structurally complex εn phase, while the Al70Pd25Co5 alloy was composed of εn 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 Al70Pd25Co5 alloy have been observed, indicating individual breakdown and re-passivation events on the sample surface. A preferential corrosion attack of εn was found, while the binary δ phase (Al3Pd2) remained free of corrosion. A de-alloying of Al from εn and formation of intermittent interpenetrating channel networks occurred in both alloys. The corrosion behavior of εn is discussed in terms of its chemical composition and crystal structure. The corrosion activity of εn could be further exploited in preparation of porous Pd−Co networks with possible catalytic activity