New approach to mimic rheological actual shear rate under wall slip condition

Engineering with Computers - The presence of wall slip in concentrated suspensions affect the rheological measurements such as shear stress, shear rate, and viscosity. The measured shear rate will...     

Adsorption of Uranium from Aqueous Solutions by Expanded Perlite

Radiochemistry - The uranium removal from radioactive liquid waste using expanded perlite (EP) was studied. The influence of the contact time, solution pH, initial uranium concentration, sorption...     

The electroremoval of copper from dilute waste solutions using Swiss-roll electrode cell

Copper is usually present in concentrations less than 5 g/L⁻¹ in dilute waste solutions. The low concentrations make these solutions unsuitable for the electro-flow owinning processes via conventional electrolysis cells. Unconventional, two-and three-dimensional electrode cells with relatively large cathodic area are essential for such treatment. Different types of cells are mentioned in the literature. Among these cells, the two-dimensional Swiss-roll cell (SR) is considered in this study. The effects of cathodic current densities, initial copper concentrations, free sulfuric acid concentration, the presence of iron and zinc cations, and the rate of flow of the solution on both the cathodic current efficiency and power consumption were studied. Copper was removed from synthetic and industrial mixtures of Cu/Fe/Zn sulfate solutions to less than 5 ppm with power consumptions of 10.326 kWh/kg⁻¹ and 8.61 kWh/kg⁻¹, respectively. The correlation between the SR cell and packed-column cell on such treatment was also considered.     

Use of cryogenic machining to improve the adhesion of sphene bioceramic coatings on titanium substrates for dental and orthopaedic applications

Rods of commercially pure titanium were machined using standard oil-based emulsion and cryogenic cooling, and were then coated with sphene (CaTiSiO₅) bioceramic by spray coating using an automatic airbrush. The sphene bioceramic was synthesized in-situ starting from a suspension of polysiloxane that used as SiO₂ precursor, CaCO₃ and TiO₂ nanoparticles. The suspension was deposited on the machined substrates, which were heat treated up to 950?°C in order to promote the formation of sphene ceramic. The produced coated prototypes were characterized to evaluate the effect of the machining conditions on surface roughness and microstructure of the substrate, and thereby their effect on coating adhesion. Nanoindentation tests were employed to determine the hardness and elastic modulus of the coating through its thickness. Results showed that the reduced amount of defects on the surface of the cryo-machined substrates, contributed to increase the hardness, elastic modulus and adhesion strength of the coating-substrate interfaces compared to standard machined samples, therefore improving adhesion of the coating to the underlying substrate.     

Chemically induced graft copolymerization of 4-vinyl pyridine onto carboxymethyl chitosan

A novel super absorbent polymer was prepared by graft copolymerization of 4-vinyl pyridine (4VP) onto the chains of carboxymethyl chitosan in aqueous solution using potassium persulphate (KPS) as initiator. The effect of monomer and initiator concentration, reaction temperature, and time on the grafting yield has been investigated. The maximum grafting yield was achieved at [KPS] = 4 × 10⁻² mol/L, [M] = 2.5 mol/L at reaction temperature = 60 °C within reaction time = 3 h. The molecular structure of the graft copolymer was confirmed by FTIR, surface morphology before and after the polymerization was examined by SEM. Different analyses were done for the graft copolymer such as X-ray diffraction, solubility tests, and thermal analysis. Different applications were done on the graft copolymer such as swell ability in different pH solutions, dye, and metal uptake.     

Synthesis,Characterization and Surface Activity of New Eco-friendly Schiff Bases Vanillin Derived Cationic Surfactants

Three eco-friendly cationic surface active agents were synthesized from the chemical modification of vanillin. The chemical structures of these surfactants were confirmed using elemental analysis, IR and NMR spectra. The surface activity measurements showed their high tendency towards adsorption and micellization and their good surface tension reduction, low interfacial tension. The emulsion stability measurements showed acceptable efficiency as emulsifying agents for short term emulsions. The biodegradability tests revealed that these compounds are eco-friendly and had completely degraded in 30 days.     

Effect of chemical modification of oil fly ash and compatibilization on the rheological and morphological properties of low‐density polyethylene composites

In this study, the effect of oil fly ash (OFA), a by‐product of oil fuel power plants, on the rheological and morphological behavior of low‐density polyethylene (LDPE) is investigated. As received and acid‐functionalized OFA (COOH‐OFA) are used to examine the effect of surface modification of OFA on polymer–filler composites. LDPE/OFA composites were prepared by melt mixing with filler loading in the range 1–10 wt %. The results are compared with pure LDPE. The effect of polyethylene‐grafted‐maleic anhydride (PE‐g‐MA) as a compatibilizer was also studied. Both viscous and elastic properties of composites increased with OFA loading especially at low frequency. The surface modification of OFA has influenced the properties of OFA. As‐received OFA showed some agglomeration at high loading that resulted in two‐phase system as described by scanning electron microscopy (SEM) and Cole–Cole plot. Field emission‐SEM (FE‐SEM) images showed improvement in the dispersion of COOH‐LDPE/OFA composites. In addition, the surface modification reduced the size of agglomeration. In general, the COOH modification of OFA improved both the dispersion and rheological properties of OFA. With chemical modification, the concentration of the filler can be increased to 10% without compromising the properties of the composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

Influence of Single-Walled Carbon Nanotubes on the Performance of Poly(Azomethine-Ether) Composite Materials

The present work is aimed to fabricate a new set of composite materials containing conducting poly(azomethine-ether) reinforced with single-walled carbon nanotubes in the form of single-walled carbon nanotube/poly(azomethine-ether)_1–5 for excellent enhanced thermal as well as conducting behavior of poly(azomethine-ether). Single-walled carbon nanotubes of variable loading have been embedded into conducting poly(azomethine-ether) using in situ polymerization technique. Before attempting the polymerization, 1,3-thiazole established poly(azomethine-ether) and its conformable monomers have been prepared and their chemical structures have been correlated by spectral analyses. Furthermore, η_inh and M_w values for poly(azomethine-ether) were found 0.89?dL?g^?1 and 39723.6, respectively. The fabricated single-walled carbon nanotube/poly(azomethine-ether)_1–5 composites were specified and characterized by wide-angle X-ray diffraction patterns, Fourier transform infrared spectroscopy, thermal behavior, scanning electron microscopy, and transmission electron microscopy characterization techniques. A perfect indicative response for this composite material was estimated by Fourier transform infrared spectra and X-ray diffraction as well. Both techniques displayed all intensive characteristic peaks regarding single-walled carbon nanotubes and poly(azomethine-ether) in the spectra or diffraction pattern for single-walled carbon nanotube/poly(azomethine-ether)_1–5. The role of single-walled carbon nanotubes on the performance of poly(azomethine-ether) was considerably examined. Single-walled carbon nanotube/poly(azomethine-ether)_1–5 showed relatively higher thermal stability. Single-walled carbon nanotube/poly(azomethine-ether)₁ displayed the lowest final composite degradation temperature value (552°C), whereas single-walled carbon nanotube/poly(azomethine-ether)₅ displayed the highest value (621°C). T₁₀ and T₂₅ values showed a gradual temperature increased while single-walled carbon nanotubes increased. Single-walled carbon nanotube/poly(azomethine-ether)₁ showed the lowest thermal stability and single-walled carbon nanotube/poly(azomethine-ether)₅ showed the highest thermal stability between all fabricated products. Furthermore, transmission electron microscopy images showed a prominent increase in single-walled carbon nanotubes diameters (40–60?nm). The conductivity values were significantly increased while single-walled carbon nanotubes content was increased and reached to the semiconductors. ε′ values were also increased in both single-walled carbon nanotube/poly(azomethine-ether)_4,5 which have higher single-walled carbon nanotubes content.