Physicochemical properties of nanopowdered eggshell

This study was carried out to investigate the physicochemical properties of nanopowdered eggshell (NPES). These characteristics were determined based on the particle size, particle morphology, zeta potential, moisture sorption behaviour, purity and crystallinity. Homogeneous, aggregated and spherical crystals of NPES particles were observed through scanning electron microscope and transmission electron microscope. The average particle sizes of NPES and powdered eggshell (PES) were 202.3 ± 28.9 nm and 113.89 ± 79.37 μm, respectively. Zeta potentials of NPES (?15.41 mV) suggested an incipient instability of the colloidal system. Moisture sorption analysis indicated a higher water adsorption capacity of NPES than that of PES. X‐ray diffractometer (XRD) analysis confirmed the presence of calcite in both NPES and PES. The chemical compositions of the NPES and PES particles were strongly associated with the presence of calcium carbonate, as determined by the Fourier transform infrared (FTIR) spectra. Therefore, eggshell nanopowder has a great potential to be utilised as a component for biomedical applications.     

Logarithmic decrease of adhesion force with lateral dynamic revealed by an AFM cantilever at different humidities

Adhesion forces between a tipless cantilever and an Au film were determined to investigate the influence of lateral velocity by recording force curves with an atomic force microscope at 20%–90% relative humidities. The sample was moved laterally, forth and back, with a frequency of 0.001–100 Hz and scan distances of 0.8, 8, and 80 μm to achieve a velocity ranging over 7 orders of magnitude. Experimental results show that at low lateral velocities (between 1.6 nm/s and 1–10 μm/s), the adhesion force either increases or decreases or remains stable with the lateral velocity without a certain characteristic trend. However, after a critical velocity, the adhesion force decreases logarithmically with the lateral velocity (between 1–10 and 16,000 μm/s). The decreasing magnitude can be as large as 97.3% of the maximum adhesion force. This decrease is well-explained by the contact time dependence of water bridges formed by capillary condensation.     

Extrusion of silicon-rich AlMgSi alloys

As a part of on-going research on phase transformations during the deformation of light alloys, the effect of silicon excess on the extrudability and mechanical properties of the standard AlMgSi1 alloy within AA6082 alloy is investigated in this study. The AlMgSi1 alloy and three experimental aluminum alloys with a silicon content of 1.98%, 3.73% and 5.51% were direct-chilled cast into billets 95 mm in diameter, homogenized at 540 °C for 4 h and extruded into 12 mm diameter rods at different extrusion speeds. The results showed that an increase in the silicon content reduced the extrudability of the AlMgSi1 alloy by lowering the limiting extrusion speed. However, the extruded alloys with 3.73% and 5.51% silicon, generally characterized by a fine grained microstructure, exhibited higher strength levels compared with the 1.98% silicon alloy. Nonetheless, the mechanical properties of these alloys, in the T6 temper condition, were below those of the AlMgSi1 base alloy.     

Method for measuring thermal contact resistance of graphite thin film materials

Thermal contact resistance (TCR) is an important parameter in thermal analysis of materials. Because of many influential factors, it is difficult to find a general model or computational formula to calculate the TCR of a solid interface. In many engineering applications, TCR values are usually obtained through experiments. Unlike extensive research focusing on ordinary columnar materials, this paper aims at measuring the TCR values of graphite thin film materials. The technical challenge is that it is not convenient to embed thermocouples into such materials. To overcome this challenge, a steady-state method using a copper heat flux meter is developed, which provides a useful tool for indirect TCR measurement. In our experiments, the TCR values of the graphite thin film materials are successfully measured under different temperature and pressure levels. The results provide a valuable guideline for the use of this type of material in high-temperature, high-pressure applications.     

Porous shell/dense core structures prepared in tungsten phosphate glass through template-free route

The preparation of the 11.7Li₂O–39.7WO₃–10.9CaO–37.7P₂O₅ glass (pgLWCP) was based on a one-step heat treatment of the 6Li₂O–18WO₃–43CaO–33P₂O₅ (gLWCP) glass followed by leaching of the β-Ca₂P₂O₇ phase formed during the crystallization process. The porous structure was formed in the region formerly occupied by the β-Ca₂P₂O₇ phase. The gLWCP undergoes devitrification through surface crystallization. This process occurs after a thermal treatment in lower temperature and in a shorter period of time than that required for the complete crystallization. After acid leaching treatment, we obtained a core-/shell-like structure with a very well-defined dense glass (gLWCP)/porous glass (pgLWCP) interface. The pgLWCP exhibits reversible coloration–decoloration reactions.     

Fabrication and analysis of cylindrical resin AFM microcantilevers

In this paper a new method of fabricating cylindrical resin microcantilevers using the Direct Digital Manufacturing (DDM) technique of Micro-stereolithography (MSL) is described. The method is rapid and commercially viable, allowing the fabrication of atomic force microscope (AFM) cantilevers which exhibit much larger spring constants than those currently commercial available. This allows for experimentation in a force regime orders of magnitude higher than currently possible using the AFM. This makes these cantilevers ideally suited for AFM-based depth sensing indentation. Due to their geometry, the assumptions used in the standard Euler-Bernoulli beam theory usually used to analyse AFM cantilevers may no longer be valid. Therefore approximate analytical solutions based on Timoshenko beam theory have been derived for the stiffness and resonant frequency of these cantilevers. Prototypes of the cantilevers have been fabricated and tested. Results show good agreement between experiment and theory.     

Fe-Co薄膜与Al2O3 基体相互扩散和相互作用相关的微观结构演变

利用先进分析透射电子显微镜,检测并系统地研究了磁控溅射Fe-Co薄膜与Al₂O₃基体之间的相互扩散。结果表明,扩散会形成尖晶石相FeAl₂O₄,并导致界面层的形成。微观结构表征表明,在界面附近的Fe-Co薄膜中形成了与相互扩散相关的非公度结构。本研究不仅检测到Fe-Co薄膜与蓝宝石基体之间的相互扩散和伴随的新相形成,而且揭示了界面区域相应的微观结构演变,这些结果可能对薄膜的磁学性质有很大的影响。     

Lactoperoxidase-mediated degradation of single-walled carbon nanotubes in the presence of pulmonary surfactant

Carbon nanotubes (CNTs) may elicit inflammatory responses following pulmonary exposure. Conversely, enzymatic biodegradation of CNTs by inflammatory cells has also been reported. The aim of this study was to study the degradation of oxidized single-walled CNTs (ox-SWCNTs) by lactoperoxidase (LPO), a secreted peroxidase present in the airways, and whether pulmonary surfactant affects this biodegradation. To this end, ox-SWCNTs were incubated in vitro with recombinant bovine LPO + H₂O₂ + NaSCN in the presence and absence of porcine lung surfactant (Curosurf®) and biodegradation was monitored using UV–Vis–NIR spectroscopy, Raman spectroscopy, and scanning electron microscopy. The interaction of recombinant LPO with bundles of ox-SWCNTs was confirmed by atomic force microscopy. Cell-free biodegradation of ox-SWCNTs was also observed ex vivo in murine bronchoalveolar lavage fluid in the presence of H₂O₂ + NaSCN. Our study provides evidence for biodegradation of ox-SWCNTs with a lung surfactant ‘bio-corona’ and expands the repertoire of mammalian peroxidases capable of biodegradation of ox-SWCNTs. These findings are relevant to inhalation exposure to these materials, as LPO serves as an important component of the airway defense system.