Laser welding of thin foil nickel-titanium shape memory alloy

In this study, two L27 Taguchi experiments were carried out to study the effect of fibre laser welding parameters and their interactions upon the weld bead aspect ratio of nickel-titanium thin foil. The optimum parameters to produce full penetrated weld with the largest aspect ratio and desirable microstructure were successfully obtained by the Taguchi experimental design. The corrosion property of the optimized NiTi weld in Hank’s solution at 37.5 °C was studied and compared with the as-received NiTi. To improve the corrosion properties of the weld, the effect of post-weld-heat-treatments ranging from 573 to 1173 K was investigated. The corrosion properties, surface morphology, microstructure and Ti/Ni ratio of the heat-treated NiTi weld were analysed. It was found that a post-weld heat treatment at 573 K for 1 h provided the best pitting corrosion resistance at the weld zone.     

A fluorine-contained copolymer ultra-thin film: Stability and electrochemical corrosion behavior

A novel fluorine-contained random copolymer (2,3,4,5,6-pentafluorostyrene)-r-poly(4-vinyl benzocyclobutene) (P(PFSt-r-4-VBCB)) was synthesized, and then spin-coated onto Si substrates followed by thermal cross-linking to produce the copolymer ultra-thin films. Although the surface modification with the P(PFSt-r-4-VBCB) film was simple and did not rely on special surface chemical reactions, the film could decrease the surface energy significantly, more importantly; the film demonstrated excellent stability and corrosion resistance. This random copolymer film could find broad applications in modifying various solid surfaces to enhance the properties such as corrosion resistance and solvent resistance.     

Corrosion Products Formed on Mild Steel Samples Submerged in Various Aqueous Solutions

Corroded samples, from the steel shell of an industrial evaporator system were investigated. A protective magnetite layer had formed, which subsequently dissolved in localised areas, resulting in failure of the shell. To clarify the mechanisms involved, mild steel samples of similar composition to the steel shell were submerged in the condensate and experiments were performed at room temperature and at 90°C under both static and dynamic conditions for exposure times up to 30 days. Control samples were submerged in deionised water under similar conditions. The dynamic corrosion rates in the industrial condensate were a factor of 2 higher than the rates for the deionised water, whilst static corrosion rates, measured in both media, were lower by a factor of 3 to 4 found for the dynamic experiments. The corrosion products were identified by means of CEMS analyses. The main components were magnetite and oxyhydroxides of iron. Additional to the species mentioned, -Fe₂O₃, goethite and hematite formed.     

Fe–Mn–Al–C Alloys: a Study of Their Corrosion Behaviour in SO2 Environments

The corrosion reaction of four Fe–Mn–Al alloys exposed to a cycling, dry–humid, SO₂ (0.001% by volume) polluted atmosphere was studied. ICEMS, XPS, AES-SAM and transmission Mössbauer spectroscopy at different temperatures were employed to characterize the corrosion products. The analytical results indicate that (i) ferrihydrite is the main component of the rust; (ii) there is an abundant presence of Mn²⁺ and SO₃ ^2–/SO₄ ^2– on the top of the corrosion layer, the concentration of SO₄ ^2– increasing with the number of cycles; and (iii) the magnetic hyperfine pattern exhibited by the series of low-temperature spectra of the rust is quite different from that observed in the rust formed under similar corrosive environments on iron and weathering steel. This latter finding is correlated with a slow rate of transformation of the Fe³⁺ species formed at the early stages of corrosion into -FeOOH, the usual final product of this type of corrosion processes. The sulphate anions, abundant inside the electrolyte during the wet periods, could be incorporated to the ferrihydrite structure being responsible for the Mössbauer spectral pattern recorded from the corrosion products at low temperatures.     

Corrosion behavior of low energy,high temperature nitrogen ion-implanted AISI 304 stainless steel

This work presents the results of a low-energy nitrogen ion implantation of AISI 304 type stainless steel (SS) at a moderate temperature of about 500°C. The nitrogen ions are extracted from a Kauffman-type ion source at an energy of 30 keV, and ion current density of 100 μA cm⁻². Nitrogen ion concentration of 6 × 10¹⁷, 8 × 10¹⁷ and 10¹⁸ ions cm⁻², were selected for our study. The X-ray diffraction results show the formation of CrN polycrystalline phase after nitrogen bombardment and a change of crystallinity due to the change in nitrogen ion concentration. The secondary ion mass spectrometry (SIMS) results show the formation of CrN phases too. Corrosion test has shown that corrosion resistance is enhanced by increasing nitrogen ion concentration.      

Ce conversion and electrolysis surface treatments applied to A3xx.x alloys and A3xx.x/SiCp composites

The influence of different variables (stirring, degreasing, oxidant additions, pH, Ce concentration, anion type, time and temperature of immersion) on the optimization of Ce conversion and electrolysis coatings on both A3xx.x alloys and aluminium metal matrix composites A3xx.x/SiCp was evaluated in 3.5 wt% NaCl at 22 °C using potentiodynamic polarization. Ce treated surfaces presented better corrosion behaviour in chloride media than original material surfaces without treatment. Both treatments preferentially covered the intermetallic compounds and SiCp. The electrolysis afforded a higher degree of protection than conversion treatment because the coating was more extensive. Coating microstructure was analysed by scanning electron microscopy (SEM), atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS).     

Surface analysis of a cold leg section of an SS316-lithium loop

Compatibility studies of austenitic stainless steel AISI 316 with liquid lithium for fusion application have shown that a porous ferritic layer is formed on the surface of the steel in the hot leg of a loop experiment due to depletion of alloying elements. The concentration profiles of the removed elements across the cross section of the tube reveal a pronounced step between the austenite matrix and the porous ferrite which is not expected in a normal diffusion process. The removed elements are partly deposited on the surface of the cold leg.In this study we looked at the boundary between the nickel rich deposit and the original matrix of a section of the cold (435 °C) leg. On the surface of the austenite, the expected grain boundary attack of lithium was observed. Additionally, to a depth of about one grain size, chromium and molybdenum were depleted and lithium seemed to also have attacked the bulk material, resulting in a splitting up into smaller grains with decomposed concentrations of the alloying elements, i.e. iron with large amounts of nickel and iron with chromium and small nickel amounts.In this paper a suggestion is put forward describing a reaction mechanism leading to the porous layer in the hot leg as a result of the instability of AISI 316 and its decomposition into two phases under the influence of liquid lithium.Dedicated to Professor Günther Tölg on the occasion of his 60th birthday     

四种三唑化合物的合成及它们在盐酸介质中对碳钢缓蚀性能的研究

本文通过“点击化学”的方法合成了四种1,2,3-三唑化合物(3a, 3b, 4a和4b)，通过IR, ¹H NMR, ¹³C NMR 和 single crystal X-ray 晶体结构衍射分析对化合物进行了表征。通过交流阻抗和动电位扫描极化曲线研究四种化合物在1 mol/L HCl 中对碳钢的缓蚀性能。研究结果表明，四种化合物均可作为高效阳离子缓蚀剂，其中化合物4b的缓蚀效果最好，最高抑制效率可达97％。     

Electrodeposition and characterization Zn-Co alloy

The present work details optimization of a stable acid chloride bath for electroplating of bright Zn-Co alloy on mild steel using gelatin and glycine as additives. It was found that the addition of gelatin along with glycine changed the deposition pattern markedly. A suitable bath has been formulated using conventional Hull cell experiments. The bath under plating conditions were found to exhibit anomalous codeposition with preferential deposition of less noble (zinc) over more noble (cobalt) as characterized by Zn-Fe group metal alloys. Investigation revealed that the current density (c.d.), temperature, and pH of the bath have strong effect on the composition of the deposit. Influence of bath constituents and operating parameters on appearance and composition of deposits were studied as measure of their performance against corrosion. A variety of deposits were obtained and their corrosion resistances were measured by Tafel method with/without chrome passivation. Experimental results demonstrated the fact that the corrosion resistances of Zn-Co alloys increased with percent of Co in the deposit except at very high c.d. This is due to the fact at very high c.d. the deposit becomes very porous and thick as evidenced by SEM image. The formation of Zn-Co alloy is confirmed by EDAX analysis. A stable chloride bath for Zn-Co alloy deposition has been proposed and discussed. The formation of passive film on chromatization is indicated by almost same E _corr value of all Zn-Co electroplates irrespective of the current densities at which they have been deposited. Published in Russian in Elektrokhimiya, 2009, Vol. 45, No. 7, pp. 811–816. The text is published in the original.