Comparison of the Microstructure and Mechanical Properties of As-Cast A356/SiC MMC Processed by ARB and CAR Methods

Accumulative roll bonding (ARB) and continual annealing and roll-bonding (CAR) processes were used in this study for improving the microstructure and mechanical properties of the A356/10?vol.% SiC metal matrix composite (MMC) produced by semi-solid metal processing (SSM). The results showed that using the ARB and CAR processes led to the following points: (a) the uniformity of the silicon and silicon carbide in the aluminum matrix improved, (b) the Si particles became finer and more spheroidal in appearance, (c) the porosity disappeared, (d) the bonding quality between the reinforcement and the matrix improved, (e) the particle-free zone disappeared, and therefore (f) the tensile strength (TS), elongation, and formability index of the MMC samples improved. However, it was found that the CAR process is a better method for improvement of microstructure and mechanical properties of as-cast MMC compared to ARB process.     

Flavonone 3-hydroxylase Relieves Bacterial Leaf Blight Stress in Rice via Overaccumulation of Antioxidant Flavonoids and Induction of Defense Genes and Hormones

Efficient accumulation of flavonoids is important for increased tolerance to biotic stress. Although several plant defense mechanisms are known, the roles of many pathways, proteins, and secondary metabolites in stress tolerance are unknown. We generated a flavanone 3-hydroxylase (F3H) overexpressor rice line and inoculated Xanthomonas Oryzae pv. oryzae and compared the control and wildtype inoculated plants. In addition to promoting plant growth and developmental maintenance, the overexpression of F3H increased the accumulation of flavonoids and increased tolerance to bacterial leaf blight (BLB) stress. Moreover, leaf lesion length was higher in the infected wildtype plants compared with infected transgenics. Kaempferol and quercetin, which scavenge reactive oxygen species, overaccumulated in transgenic lines compared with wildtypes in response to pathogenic infection, detected by scanning electron microscopy and spectrophotometry. The induction of F3H altered the antioxidant system and reduced the levels of glutathione peroxidase activity and malondialdehyde (MDA) contents in the transgenic lines compared with the wildtypes. Downstream gene regulation analysis showed that the expression of F3H increased the regulation of flavonol synthase (FLS), dihydroflavonol 4-reductase (DFR), and slender rice mutant (SLR1) during BLB stress. The analysis of SA and JA signaling revealed an antagonistic interaction between both hormones and that F3H induction significantly promoted SA and inhibited JA accumulation in the transgenic lines. SA-dependent nonexpressor pathogenesis-related (NPR1) and Xa1 showed significant upregulation in the infected transgenic lines compared with the infected control and wildtype lines. Thus, the overexpression of F3H was essential for increasing BLB stress tolerance.     

VAPOR-LIQUID EQUILIBRIA OF TOLUENE + n-BUTANOL AND TOLUENE + n-BUTANOL + CALCIUM CHLORIDE AT 94.0kPa

Vapor-liquid equilibrium data of toluene + n-butanol and toluene+ n-butanol + CaCl₂ (at saturation) were measured at a pressure of 94.0 kPa, using a modified Malanowski equilibrium still. The salt investigated in this work, i.e., CaCl₂, exhibits a slight salting-out effect on toluene. The experimental results of the salt-free binary were compared with those obtained from NRTL, ASOG, and UNIFAC models. The latter two models predicted the bubble-point temperatures within 0.5 K (as a root mean square deviation, RMSD) whereas the NRTL model, which was employed to establish thermodynamic consistency by directly fitting the experimental data, correlated the bubble-point temperatures with an RMSD of 0.2 K. On the other hand, the experimental data of toluene+n-butanol+CaCl₂ were compared with those predicted by the NRTL-Tan model for the effect of the electrolyte. This model predicted the bubble-point temperatures with an RMSD of 0.5 K. Calcium chloride has been shown not to have a sensible effect on the azeotropic composition.     

Glass transition behaviors of interfacially polymerized polyamide barrier layers on thin film composite membranes via nano-thermal analysis

Thin film composite (TFC) reverse osmosis (RO) membranes enjoy widespread use in desalination, but their sensitivity to oxidizing agents such as chlorine remains a continuing challenge. In contrast to many reports on the chemical aspects associated with decreased membrane performance after chlorine exposure, studies on the fundamental physical properties of the polyamide barrier layer (PBL) of TFC membranes are scarce. This omission is mostly due to the lack of techniques capable of characterizing such interfacially polymerized PBLs, which are ultrathin and insoluble. The focus of this study is the development of an AFM-based nano-thermal analysis technique that provides the first-ever result for the direct measurement of the glass transition temperature (T_g) of the PBL on several commercial TFC RO membranes. Moreover, the technique is utilized to study the changes in T_g of the PBL after exposure to chlorine solutions as a function of concentration and duration at constant pH. Results indicate significant and systematic reduction in T_g of the PBL with increasing chlorine concentration and exposure time.     

Adsorption of bromo-phenol blue from an aqueous solution onto thermally modified granular charcoal

The adsorption phenomenon of bromo-phenol blue onto pristine and thermally evacuated granular charcoal (GC) was studied via a batch technique at 25 °C. The effect of evacuation temperature on the GC surface and pore structure (e.g. pore volume and diameter) was studied by Fourier transform infrared spectroscopy (FT-IR), point of zero charge (PZC), proximate analysis, Brunauer, Emmett and Teller (BET) method and field emission scanning electron microscopy (FE-SEM). The FT-IR spectra of the samples after evacuation showed considerable decrease in the acidic functional groups. PZC showed that the surface of the evacuated charcoal became basic as the evacuation temperature was increased from 300 to 800 °C. Volatile matter decreased while ash and fixed carbon contents increased during evacuation, which led to an increase in the micro-pore volume from 0.25 to 0.42 cm³ g⁻¹, meso-pore volume from 0.04 to 0.13 cm³ g⁻¹, pore diameter from 5.01 to 6.21 nm, and specific surface from 150.32 to 254.70 m² g⁻¹. Adsorption of the bromo-phenol blue onto charcoal, increased as the evacuation temperature was increased from 300 to 800 °C. The interaction of bromo-phenol blue with charcoal was proposed to have occurred via hydrogen bonding. The adsorption data fitted well with the Langmuir equation, which indicated that the monolayer adsorption has occurred at specific sites within the adsorbent.     

Effect of pH on Aerobic Granulation and Treatment Performance in Sequencing Batch Reactors

Two sequencing batch reactors were operated to investigate the effect of influent alkalinity and reactor pH on aerobic granulation. In the first reactor R1 with high influent alkalinity the pH was adjusted in the neutral range, and in the second reactor R2 with low alkalinity the pH was held within the acidic range. The R1‐dominating species were bacteria and the appearance time of granules was three weeks after reactor start‐up. On the other hand, the acidic environment of R2 provided favorable conditions for fungal growth, and rapid granule formation occurred within the first week of operation. The varying microbial structure of granules resulted in different reactor performance in terms of evolution time and morphology of granules, suspended solids in the reactors, settling ability of granules, effluent quality of treated wastewater, and physical strength of the granules.     

Optimization of mechanical properties of in situ polymerized poly(methyl methacrylate)/alumina nanoparticles nanocomposites using Taguchi approach

Polymer Bulletin - Alumina nanoparticles are among important metal oxides with specific properties but chemically incompatible with an organic matrix such as poly(methyl methacrylate) (PMMA). In...     

Microstructural study of synthesized polyethylenes by homogeneous and heterogeneous nickel α-diimine catalysts

In this work, ethylene polymerization was investigated by using homogeneous and heterogenouse nickel α-diimine catalysts [1,4-bis(2,6-diisopropylphenyl) acenaphthene diimine nickel(II) dibromide]. Methyl aluminoxane (MAO) and triethyl aluminum (TEA) were used as cocatalysts in homogenous and heterogeneous polymerizations, respectively. The heterogeneous catalyst showed lower activity than its homogeneous equivalent. The influence of polymerization temperature and heterogenization conditions was studied on the microstructure properties of the prepared polymers. Increasing polymerization temperature (T _P) up to 50 °C decreased the activity of both homogenous (LN) and heterogeneous (LNS) nickel α-diimine catalysts. The highest activities were 1286 and 982 kg PE (mol Ni bar h)^?1 obtained at T _P = 30 °C for LN and LNS catalysts, respectively. The polymer samples obtained by supported catalyst (LNS) showed lower unsaturation contents. Moreover, DSC analysis did not show any melting peaks for polymers obtained by LN catalyst due to their amorphous structure, which was confirmed by XRD analysis. The microstructure of the prepared polymers was completed by successive self-nucleation annealing (SSA) and was investigated by ¹³C NMR studies. The SSA thermogram of samples made by LNS catalyst exhibited several crystal types with different lamella thicknesses. The branches in polyethylene samples produced by homogenous catalyst were higher and showed more diversity. The total methyl branch percentages for both LN and LNS catalysts were 13.1 and 3.4%, respectively.     

Green bio-synthesis of Ni/montmorillonite nanocomposite using extract of Allium jesdianum as the nano-catalyst for electrocatalytic oxidation of methanol

In this work, synthesis of Ni nanoparticles was carried out successfully by water extract of Allium jesdianum as a biochemical reducing agent in the presence of montmorillonite clay (MMT) as a natural solid support for the first time. Then the electrochemical activity of the synthesized nanocomposite was investigated in methanol electrocatalytic oxidation. MMT with high cation exchange capacity and nano layer structure was exposed to ion exchange conditions in nickel solution. Then Ni²⁺ ion exchanged form was used in this process as a source of ions and also capping agent. Water extract of Allium jesdianum used as a reducing agent due to abundant availability of phenolic and flavonoid contents. The synthesized Ni/MMT nanocomposite was characterized using UV–Vis spectroscopy (UV–Vis), Fourier Transform Infrared Spectroscopy (FT-IR), X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission electron microscopy (TEM) and Energy-dispersive X-ray spectroscopy (EDX). The surface of prepared modified electrode has been characterized using SEM to evaluate the morphology, showing uniform dispersion of Ni nanoparticles with mean diameter of 12 to 20 nm. The modified carbon paste electrode was then used in methanol electrocatalytic oxidation reaction. Methanol oxidation on the proposed modified electrode surface occurs at 0.6 V and 0.3 V in alkaline and acidic medium respectively. Also, the results showed the better performance of modified electrode toward methanol electrocatalytic oxidation in comparison with carbon paste electrode that is modified by ion exchanged MMT. Charge transfer coefficients and apparent charge transfer rate constant for the modified electrode in the absence of methanol in alkaline medium were respectively found as: α_a = 0.53, α_c = 0.37 and k_s = 1.6 × 10⁻¹ s⁻¹. Also, the average value of catalytic rate constant for the electrocatalytic oxidation of methanol by the prepared nano-catalyst was estimated to be about 0.9 L·mol^-1·s^-1 by chronoamperometry technique. The prepared electrode was also effective for electrocatalytic oxidation of ethanol and formaldehyde in alkaline medium.     

Study of the effect of the concentration,size and surface chemistry of zirconia and silica nanoparticle fillers within an epoxy resin on the bulk properties of the resulting nanocomposites

Epoxy resin nanocomposites were prepared by curing bisphenol‐F with an aliphatic amine in the presence of SiO₂ and ZrO₂ nanoparticles as inorganic fillers. Both types of particles were prepared with diameters of around 10 nm and 70 nm to study size effects in the nanocomposites. The nanoparticles showed a different constitution: while silica was amorphous and spherical in nature, zirconia was crystalline and non‐spherical. Both nanoparticles were surface‐functionalized with novel diethylene‐glycol‐based capping agents to increase the compatibility with the epoxy matrix. The organic functionalities were attached to the nanoparticle surface via phosphonic acid (zirconia) and trialkoxysilane (silica) anchor groups. The homogeneity of the distribution of surface‐modified inorganic nano‐sized fillers in the matrix up to 5.8 vol% in case of silica and 2.34 vol% in case of zirconia was determined by small‐angle X‐ray scattering and transmission electron microscopy. Mechanical properties such as hardness and storage modulus were increased with increasing filler content while thermal stability of the obtained materials was nearly unaffected after incorporation of nanoparticles. Copyright © 2011 Society of Chemical Industry