Flexural and Charpy impact behaviour of epoxy/glass fabric treated by nano-SiO2 and silane blend

A sizing formulation, containing compatible and incompatible silane coupling agents with epoxy resin in conjunction with nanoscale colloidal silica, was used to modify the surface of glass fabric. The modified glass fabric/epoxy resin composite panels were fabricated and characterised by flexural test, Charpy impact test and scanning electron microscope (SEM). By combining nano silica with silane blend in the fabric sizing, more energy was consumed under bending and impacting, which resulted in an improvement of the toughness in composites. The flexural strength, bending stain and Charpy impact strength of the epoxy composite/glass fabric treated with 1?wt-% nano silica and silane blend were ～42, ～22 and 35%, respectively, higher than those of silane blend coated glass fabric-reinforced composites (without nano silica). Furthermore, the change of the brittle fracture of the composite into ductile fracture was investigated by SEM micrographs. A possible toughening mechanism was also proposed.     

Synthesis of water dispersible reduced graphene oxide via supramolecular complexation with modified β-cyclodextrin

A noncovalent functionalization of the edges of reduced graphene oxide (RGO) with β-cyclodextrin-graft-hyperbranched polyglycerol (β-CD-g-HPG) was successfully performed via a host-guest interaction. The results showed that β-CD-g-HPG disperses the graphene sheets better than pure β-CD or HPG. The resulted supramolecular structure is stable in neutral water medium more than one week. However, in acidic medium the host-guest interaction is collapsed and graphene nanosheets precipitate.     

Highly efficient and versatile one-pot synthesis of substituted thienylidene compounds

A novel, efficient, and very mild one-pot synthesis of methyl 2-[(Z)-4-aryl-5-morpholino-3-oxo-2,3-dihydrothiophen-2-ylidene]acetate derivatives under kinetic control has been developed. The title compounds were prepared by the reaction of thioacetomorpholides with dimethyl acetylene-dicarboxylate (DMAD) in the presence of K₂CO₃ in a non-polar solvent with excellent yields.     

Influence of a Reactive Organoclay on Polymerization and Properties of Polyurethane Nanocomposites

In this study, segmented polyurethane/clay nanocomposites were prepared via in situ intercalative polymerization of polyether polyol mixed nanoclay with toluene diisocyanate, followed by chain extending with 1,4-butanediol. The reactive prepolymer tended to gel by increasing the clay content from 0.4 to 1.5 wt.%. This unusual phenomenon was found to be caused by a catalytic effect of quaternary ammonium intercalant on the organoclay. The procedure used for intercalated nanocomposites, is confirmed by wide angle X-ray diffraction studies. Thermogravimetric analysis results demonstrated a very good increase in onset degradation temperature by adding only 0.8 wt.% of organoclay.     

Order‐reduction of parabolic PDEs with time‐varying domain using empirical eigenfunctions

A novel methodology for the order‐reduction of parabolic partial differential equation (PDE) systems with time‐varying domain is explored. In this method, a mapping functional is obtained, which relates the time‐evolution of the solution of a parabolic PDE with time‐varying domain to a fixed reference domain, while preserving space invariant properties of the initial solution ensemble. Subsequently, the Karhunen–Loève decomposition is applied to the solution ensemble on fixed spatial domain resulting in a set of optimal eigenfunctions. Further, the low dimensional set of empirical eigenfunctions is mapped on the original time‐varying domain by an appropriate mapping, resulting in the basis for the construction of the reduced‐order model of the parabolic PDE system with time‐varying domain. This methodology is used in three representative cases, one‐ and two‐dimensional (1‐D and 2‐D) models of nonlinear reaction‐diffusion systems with analytically defined domain evolutions, and the 2‐D model of the Czochralski crystal growth process with nontrivial geometry. © 2013 American Institute of Chemical Engineers AIChE J, 59: 4142–4150, 2013     

Electrooxidation of alcohols at a nickel oxide/multi-walled carbon nanotube-modified glassy carbon electrode

Electrocatalytic oxidation of methanol and some other primary alcohols on a glassy carbon electrode modified with multi-walled carbon nanotubes and nano-sized nickel oxide (GCE/MWNT/NiO) was investigated by cyclic voltammetry and chronoamperometry in alkaline medium. The results were compared with those obtained on a nickel oxide-modified glassy carbon electrode (GCE/NiO). Both the electrodes were conditioned by potential cycling in the range of 0.1–0.6 V versus Ag/AgCl in a 0.10 M NaOH solution. The effects of various parameters such as scan rate, alcohol concentration, thickness of NiO film, and real surface area of the modified electrodes were also investigated and compared. It was found that the GCE/MWNT/NiO-modified electrode possesses an improved electrochemical behavior over the GC/NiO-modified electrode for methanol oxidation.     

Numerical investigation of grooves effects on the thermal performance of helically grooved shell and coil tube heat exchanger

Heat exchangers are integral parts of important industrial units such as petrochemicals, medicine and power plants. Due to the importance of systems energy consumption, different modifications have been applied on heat exchangers in terms of size and structure. In this study, a novel heat exchanger with helically grooved annulus shell and helically coiled tube was investigated by numerical simulation. Helically grooves with the same pitch of the helical coil tube and different depth are created on the inner and outer wall of annulus shell to improve the thermal performance of heat exchanger. In the first section, thermal performance of the shell and coil heat exchanger with the helical grooves on its outer shell wall was compared with same but without helical grooves. At the second section, helically grooves created on both outer and inner wall of the annulus shell with different groove depths. The results showed that the heat exchanger with grooves on both inner and outer shell wall has better thermal performance up to 20% compared to the heat exchanger with grooves on only outer shell wall. The highest thermal performance achieves at lower flow rates and higher groove depths whereas the pressure drop did not increase significantly.     

Effect of modified single‐wall carbon nanotubes on mechanical and morphological properties of thermoplastic elastomer nanocomposites based on (polyamide 6)/(acrylonitrile butadiene rubber)

Thermoplastic elastomer nanocomposites based on acrylonitrile butadiene rubber (NBR) and polyamide 6 (PA6), with acid functionalized single‐wall carbon nanotubes (SWNT), were prepared via a direct melt‐mixing process in an internal mixer. The influence of SWNT content (0, 0.5, 1, 1.5) on morphological properties of PA6/NBR with different ratios (80/20, 70/30, 60/40) were then investigated. Characterization of nanocomposites was conducted by using transmission electron microscopy, scanning electron microscopy, differential scanning calorimetry, and mechanical properties. Scanning electron microscopy micrographs proved the droplet‐matrix blend morphology in which the size of NBR droplets decreased as the SWNT loading increased, suggesting dispersion of SWNT in the PA6 phase. It was further proved by transmission electron microscopy images, showing homogenous dispersion of SWNT in the PA6 phase. Differential scanning calorimetry results showed a slightly reduced percentage of crystallinity in samples containing SWNT. The mechanical properties of nanocomposites indicated an enhancement in tensile strength, modulus, and hardness on increasing SWNT content. J. VINYL ADDIT. TECHNOL., 22:336–341, 2016. © 2014 Society of Plastics Engineers     

Comparing thermal and mechanochemical decomposition of ammonium paratungstate (APT)

In this research, the possibility of mechanochemical decomposition of ammonium paratungstate (APT) has been studied, and compared with thermal decomposition method. For this purpose, APT powders were milled using a planetary ball mill up to 36 h and under air atmosphere. For thermal decomposition, APT powders were heated for 30 minutes at 300 and 450 °C in air atmosphere. X-ray diffraction (XRD), differential scanning calorimeter (DSC), and thermo gravimetric analyzer (TGA) were used to study the decomposition progress, and products. The XRD results showed that APT completely decomposed to WO₃ by thermal decomposition, while the final product of mechanochemical decomposition was WO₃ (H₂O)_0.5. According to DSC and TGA results, during thermal decomposition, ammonia and water released in four steps, and leaved WO₃. By mechanochemical decomposition crystal water and ammonia liberated from APT structure, but structural water of APT remained. In both methods, an X-ray amorphous phase was the intermediate product of APT decomposition.     

Characterization and microstructure study of low‐density polyethylene by Fourier transform infrared spectroscopy and temperature rising elution fractionation

Infrared spectroscopy is a powerful technique for studying the microstructure and determining the short‐chain branch distribution of polyethylene. In this work, the types and amounts of short‐chain branches in low‐density polyethylene were investigated with Fourier transform infrared spectroscopy, and a new and simple method for the determination of butyl short branches was discovered. The amount of each unsaturated species in low‐density polyethylene was also determined with Fourier transform infrared after the bromination of samples. Furthermore, the resin was fractionated by preparative temperature rising elution fractionation, and the branch distribution and melting endotherm of each fraction were analyzed with attenuated total reflectance/Fourier transform infrared and differential scanning calorimetry. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008