The NiTi shape memory alloy passivated for 90 min by autoclaving has been studied towards corrosion performance in the Tyrode’s simulated body fluid using open circuit potential and EIS measurements. The surface morphology and thickness of the oxide layer was determined by XRR. The HREM was used to observe the cross-section of the thin foil and to confirm the amorphous state of the TiO2 layer and its thickness. Electrochemical measurements revealed a good corrosion resistance at the beginning of long-term (20 days) immersion. It was found that with the increase of immersion time, the corrosion resistance of the surface deteriorated after nearly 1 day of immersion due to occurence of pitting corrosion. The EIS method was used to detailed study on the electrolyte | passive layer interfacial properties. Equivalent electrical circuit for the pitting corrosion on the passivated NiTi alloy has been applied.
Metallic nanoparticles are of great importance because of their unique physical, chemical, antimicrobial, diagnostic, therapeutic, biomedical, sensing, biosensing, catalytic and optical properties. Detailed knowledge of the atomic scale structure of these materials is essential for understanding their activities and for exploiting their potential. This paper reports structural studies of silicasupported silver, gold, palladium and platinum nanoparticles using X-ray diffraction and high-resolution transmission electron microscopy. Electron microscopy observation allowed the determination of nanoparticle sizes, which were estimated to be in the range of 45-470 Å , and their distribution. The obtained histograms exhibit a multimodal distribution of the investigated nanoparticle sizes. The X-ray diffraction data were analyzed using the Rietveld method in the form of Williamson-Hall plots, the PDFgui fitting procedure and model-based simulation. The Williamson-Hall plots provide evidence for the presence of strain in all investigated samples. The PDFgui fitting results indicate that the investigated nanoparticles consist of atomic clusters with different sizes and degrees of disorder as well as slightly different lattice parameters. The detailed structural characterization performed via model-based simulations proves that all samples exhibit a face-centered cubic type structure with paracrystalline distortion. The degree of disorder predicted by the paracrystalline theory is correlated with the sizes of the nanoparticles. The catalytic properties of the investigated noble metals are discussed in relation to their disordered structure. research papers J. Appl. Cryst. (2018). 51, 411-419 Karolina Jurkiewicz et al. Paracrystalline structure of metallic nanoparticles 415 research papers J. Appl. Cryst. (2018). 51, 411-419 Karolina Jurkiewicz et al. Paracrystalline structure of metallic nanoparticles 417 research papers J. Appl. Cryst. (2018). 51, 411-419 Karolina Jurkiewicz et al. Paracrystalline structure of metallic nanoparticles 419
In this paper we report a new nanometallic, self-activating catalyst, namely, Ni-supported Pd nanoparticles (PdNPs/Ni) for low temperature ammonia cracking, which was prepared using a novel approach involving the transfer of nanoparticles from the intermediate carrier, i.e. nano-spherical SiO2, to the target carrier technical grade Ni (t-Ni) or high purity Ni (p-Ni) grains. The method that was developed allows a uniform nanoparticle size distribution (4,4±0.8 nm) to be obtained. Unexpectedly, the t-Ni-supported Pd NPs, which seemed to have a surface Ca impurity, appeared to be more active than the Ca-free (p-Ni) system. A comparison of the novel PdNPs/Ni catalyst with these reported in the literature clearly indicates the much better hydrogen productivity of the new system, which seems to be a highly efficient, flexible and durable catalyst for gas-phase heterogeneous ammonia cracking in which the TOF reaches a value of 2615 mmolH2/gPd min (10,570 molNH3/molPd(NP) h) at 600°C under a flow of 12 dm3/h (t-Ni).
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