Modification of Polycaproamide Composites Based on 1H,1H,13H-rihydroperfluorotridecan-1-ol and Montmorillonite

Fibre Chemistry - Modification of polycaproamide by 1H,1H,13H-trihydroperfluorotridecan-1-ol immobilized on montmorillonite produced an F-containing polymer composite. The structure of the...     

Improving the Quality of Cellulose for Use in Disposable Sanitary and Hygiene Products

Fibre Chemistry - Under modern conditions the creation of materials for sanitary hygiene and medical products based on cellulose is of paramount importance. Development and improvement in this area...     

Investigation of 12 – 15 Kev Electron Transmission Through Tapered Glass Capillaries

Glass and Ceramics - The results of experimental studies of the transmission of 12 and 15 keV electron beams through tapered glass macro-capillaries are presented. Measurements showed that there is...     

Mechanical and Tribological Properties of Ca/P-Doped Titanium Dioxide Layer Produced by Plasma Electrolytic Oxidation: Effects of Applied Voltage and Heat Treatment

Plasma electrolytic oxidation (PEO) is a technique that produces a hard oxide layer on the titanium surface where its properties can be tailored by changing the process parameters or by a posterior heat treatment (HT). In this work, a TiO₂ layer with different crystallinity was produced by PEO with different applied voltages (250 to 400 V) and post-HT at 600°C. Our aim was to evaluate the influence of the PEO voltage and HT on the mechanical and tribological properties of anodized Ti. There is an increase in pore size, oxide thickness, and Ca/P ratio for the oxide layer with the applied voltage during the PEO process. X-ray diffraction (XRD) results indicated an increase in the crystalline rutile phase in the oxide layer with voltage and HT. Nanoindentation shows an increase in the oxide hardness and elastic modulus with increased voltage and HT, leading to an improvement in the wear resistance.     

Machining of NiTi-shape memory alloys-A review

The emerging trends in the development of advanced smart materials with better unique properties under different environments for a particular application fascinate the researchers and industrialists. Nickel-Titanium based shape memory alloys are exotic materials due to their unique properties such as SME, SE, high damping characteristics, high corrosion and wear resistance and biocompatibility. This article presents an overview of machining processes that can be used to machine the NiTi and its surface induced characteristics such as microhardness, surface roughness, topography, induced layer, residual stress, fatigue and phase transformation. The surface integrity characteristics are discussed for machining of NiTi-SMAs under the category of traditional, non-traditional and micro-machining with the effect of input parameters such as cutting speed, feed, depth of cut, type of lubricant and type of coating material on cutting tool. The conventional machining of NiTi alloys are quite complicated due to high toughness, severe strain hardening, fatigue hardening and distinctive property of NiTi-SMAs such as pseudoelastic and shape memory effect. From this study, non-traditional process is significantly used to machine the NiTi-SMAs due to its better results on surface integrity characteristics. Consequently, future trends are also identified for machining the NiTi-SMAs and to improve the surface integrity characteristics.     

Exact solutions to differential-difference heat and mass transfer equations with a finite relaxation time

Certain exact solutions to the linear differential-difference heat and mass transfer equations with a finite relaxation time are specified. The exact solution to the one-dimensional Stokes problem with the periodic boundary condition when a first-order volume chemical reaction occurs is given. A wide class of exact solutions to the nonlinear differential-difference heat-conduction equation with the following source is described: $$\Theta _t = div[f(T)\nabla T] + g(\Theta ), = T(r,t + \tau ),$$ where T = T(r, t) is temperature and τ is the relaxation time. Certain more complex heat conduction models with a variable relaxation time that can depend on time and a temperature gradient are also considered.     

TiB2 Powders Synthesis by Borothermal Reduction in TiO2 Under Vacuum

TiB₂ powders were synthesized by borothermal reduction in nanoscale TiO₂ with boron under vacuum. Reaction processes were investigated, and the effect of by‐product B₂O₃ was evaluated. Results showed that TiO₂ was firstly reduced by boron to form TiBO₃ and Ti₂O₃, and then to produce TiB₂ and B₂O₃ with increasing temperature. The reaction processes of TiB₂ powders synthesis included two‐step reduction in TiO₂ by boron and the removal of B₂O₃. The presence of B₂O₃, which was previously reported as the most important factor in promoting the coarsening of ZrB₂ and HfB₂ powders by borothermal reduction, did not lead to significant coarsening of TiB₂ powders. Due to the minor effect of B₂O₃, TiB₂ powders with small particle size and low oxygen content could be prepared by direct heat treatment of TiO₂ and boron at 1550°C under vacuum for 1 h. The particle size and oxygen content of synthesized TiB₂ powders were ~0.9 μm and ~1.7 wt%, respectively.     

Sintering Behavior and Dielectric Properties of Ultra‐Low Temperature Fired Silver Molybdate Ceramics

Ag₂MoO₄ ceramic was prepared by using the solid‐state reaction method, which could be sintered at 450°C for 2 h, having a relative permittivity of 8.08, a Qf value of 17 000 GHz, and a temperature coefficient of resonance frequency about ?133 ppm/°C. Ag₂MoO₄ ceramic was chemically compatible with silver but reacted seriously with aluminum to form (Ag_0.5Al_0.5)MoO₄ during the sintering. The fitting of infrared spectra and the Shannon's additive rule were employed to study intrinsic dielectric behaviors of the ceramics at microwave region. Ionic displacive polarization and the electronic polarization contributed almost equally to the dielectric permittivity of the ceramic at microwave region. The Ag₂MoO₄ ceramics could be a good candidate for ultra‐low temperature co‐fired microwave devices.     

Pt nanoparticles synthesized with new surfactants: improvement in C1–C3 alcohol oxidation catalytic activity

Platinum electrocatalysts were prepared using PtCl₄ as a starting material and 1-decylamine, N,N-dimethyldecylamine, 1-dodecylamine, N,N-dimethyldodecylamine, 1-hexadecylamine, and 1-octadecylamine as surfactants. These surfactants were used for the first time in this synthesis to determine whether the primary and/or tertiary structure and/or chain length of the surfactants, affects the size and/or activity of the catalysts in C₁–C₃ alcohol electro-oxidation reactions. Electrochemical measurements (cyclic voltammetry and chronoamperometry) indicated that the highest electrocatalytic performance was observed for the Pt nanocatalysts that were stabilized by N,N-dimethyldecylamine, and this has a tertiary amine structure with a short chain length (R = C₁₀H₂₁). The high performance may be due to the high electrochemical surface area, Pt(0)/Pt(IV) ratio, %Pt utility, and roughness factor (R _f). X-ray photoelectron spectroscopy, X-ray diffraction, atomic force microscopy, and transmission electron microscopy were used to determine the parameters that affect the catalytic activities.     

Improved electro-assisted removal of phosphates and nitrates using mesoporous carbon aerogels with controlled porosity

Three-activated carbon aerogels were synthesized by CO₂ activation of the materials prepared by the polycondensation of resorcinol and formaldehyde mixtures followed by supercritical drying. The obtained carbon aerogels were characterized and used as electrode materials for the electrosorption of sodium phosphate and nitrate. X-ray diffraction and Raman spectroscopy showed the dependence of the structural ordering of the aerogels with the resorcinol/catalyst ratio and the extent of activation. The electrosorption capacitance evaluated by cyclic voltammetry revealed large values for the activated samples containing a large contribution of mesopores, regardless the electrolyte salt. Due to an adequate combination of chemical and porous features, the desalting capacity of the activated carbon aerogel electrodes exceeded that of the as-prepared materials. The evaluation of the kinetic properties by chronocoulometric relaxation and impedance spectroscopy showed a decrease of time constant and resistances for highly mesoporous activated samples. A high deionization capacity and fast electrode discharge was detected for the deionization of sodium nitrate on the highly mesoporous activated aerogel. Data also showed the efficient electrosorption of ionic species on consecutive charge/discharge cycles, confirming the stability of the aerogel electrodes at the high applied potentials.