Pervaporation separation of toluene/n-heptane mixtures using a MSE-modified membrane: Effects of operating conditions

In this work, separation of toluene/n-heptane mixtures via pervaporation using a composite membrane was investigated. Effects of operating conditions such as feed temperature, feed composition and downstream pressure on the membrane performance were studied. Experimental results were obtained at different feed compositions (10–40 wt.%), operating temperatures (25–85 °C) and downstream pressures (2–32 mbar g). The membrane selectivity for toluene was found to be greater than that for n-heptane. According to the results, it was observed that increasing toluene concentration in the feed and operating temperature enhance the membrane swelling and increase the polymeric chain mobility. Therefore, feed concentration and temperature have the same effects on toluene selectivity and permeation flux of the membrane. Permeation flux increases and toluene selectivity decreases with increasing feed concentration and temperature. In contrary, the membrane performance enhances with decreasing downstream pressure. It was found out that for a feed with 10 wt.% of toluene, at a temperature of 85 °C and a downstream pressure of 2 mbar g, the highest PSI value of 18.371 kg/m² h (in which permeation flux = 4.610 kg/m² h and toluene selectivity = 4.985) is achieved.     

Pore-scale modeling of competition and cooperation of multispecies biofilms for nutrients in changing environments

In this article, we developed a pore-scale model of integrated lattice Boltzmann method and cellular automata to investigate competitive growth of aerobic nitrite and ammonium oxidizers in a bioreactor. The results showed that inlet nutrient concentrations have significant effects on maximum biofilm concentration, ratio of microorganisms' concentrations, growth pattern, and time. The local availability of oxygen could control the competition, resulting in different growth patterns. The coexistence of ammonium and nitrite in same inlet zone increased not only the biofilm concentration (7%) but also the ratio of microorganisms' concentrations (36%). Although this coexistence decreased the total biofilm concentration in some cases, it increased the growth rate about 25%. Changes of the maximum biomass concentration could change biofilm concentration of about 40% and microorganisms' concentrations ratio of about 30%. This framework provides a powerful tool to improve our understanding of dynamic interdependency of many complex microbial consortia systems with environments.     

Improving the mechanical,thermal and electrical properties of polyurethane- graphene oxide nanocomposites synthesized by in-situ polymerization of ester-based polyol with hexamethylene diisocyanate

Many polyols or diols have been used for the synthesis of polyurethanes (PU), however, to the best of our knowledge, PU-graphene oxide (GO) nanocomposites synthesized with ester-based polyols have been rarely studied. In this work ester-based polyol synthesized by the reaction of adipic acid and 1,4 butane diol, was in-situ polymerized with hexamethylene diisocyanate (HDI) and GO to prepare PU-GO nanocomposites. The content of GO was changed from 1 to 2.5 wt% and its effect on the mechanical, thermal and electrical properties of the samples were examined. The presence of GO more than 1.5% in the nanocomposites resulted in brittle samples and reduced the tensile strength, however, the Young’s modulus of the samples containing 1 and 1.5% was increased to 11 and 12.08-fold (275 and 302 MPa) compared to the neat PU (25 MPa), respectively. The shore A hardness of the samples was increased from 86 for PU to 96 for PUGO-1.5. The abrasion resistance of the samples was decreased by increasing the GO content. Results of the thermogravimetric analysis showed that higher amounts of GO increase the thermal stability of the samples. The chemical and physical interactions between the surface of GO nanolayers and the PU chains were confirmed by FTIR spectroscopy. The dynamic mechanical analysis of the samples showed that GO nanolayers decreased the molecular motions of the PU chains in the nanocomposites which were noticed by shifting the glass transition to the higher temperatures.     

Low‐order optimal regulation of parabolic PDEs with time‐dependent domain

Observer and optimal boundary control design for the objective of output tracking of a linear distributed parameter system given by a two‐dimensional (2‐D) parabolic partial differential equation with time‐varying domain is realized in this work. The transformation of boundary actuation to distributed control setting allows to represent the system's model in a standard evolutionary form. By exploring dynamical model evolution and generating data, a set of time‐varying empirical eigenfunctions that capture the dominant dynamics of the distributed system is found. This basis is used in Galerkin's method to accurately represent the distributed system as a finite‐dimensional plant in terms of a linear time‐varying system. This reduced‐order model enables synthesis of a linear optimal output tracking controller, as well as design of a state observer. Finally, numerical results are prepared for the optimal output tracking of a 2‐D model of the temperature distribution in Czochralski crystal growth process which has nontrivial geometry. © 2014 American Institute of Chemical Engineers AIChE J, 61: 494–502, 2015     

Combined Spectroscopic and Calorimetric Studies to Reveal Absorption Mechanisms and Conformational Changes of Protein on Nanoporous Biomaterials

In this study the effect of surface modification of mesoporous silica nanoparticles (MSNs) on its adsorption capacities and protein stability after immobilization of beta-lactoglobulin B (BLG-B) was investigated. For this purpose, non-functionalized (KIT-6) and aminopropyl-functionalized cubic Ia3d mesoporous silica ([n-PrNH₂-KIT-6]) nanoparticles were used as nanoporous supports. Aminopropyl-functionalized mesoporous nanoparticles exhibited more potential candidates for BLG-B adsorption and minimum BLG leaching than non-functionalized nanoparticles. It was observed that the amount of adsorbed BLG is dependent on the initial BLG concentration for both KIT-6 and [n-PrNH₂-KIT-6] mesoporous nanoparticles. Also larger amounts of BLG-B on KIT-6 was immobilized upon raising the temperature of the medium from 4 to 55 °C while such increase was undetectable in the case of immobilization of BLG-B on the [n-PrNH₂-KIT-6]. At temperatures above 55 °C the amounts of adsorbed BLG on both studied nanomaterials decreased significantly. By Differential scanning calorimetry or DSC analysis the heterogeneity of the protein solution and increase in Tm may indicate that immobilization of BLG-B onto the modified KIT-6 results in higher thermal stability compared to unmodified one. The obtained results provide several crucial factors in determining the mechanism(s) of protein adsorption and stability on the nanostructured solid supports and the development of engineered nano-biomaterials for controlled drug-delivery systems and biomimetic interfaces for the immobilization of living cells.     

Physical and Morphological Properties of Combined Treated Wood Polymer Composites by Maleic Anhydride and Methyl Methacrylate

Wood polymer composites were prepared by consecutive impregnation with maleic anhydride (MAN) and methyl methacrylate (MMA). Samples impregnated with MAN alone, were heated at 120°C and 150°C for 4 and 8 h. Based on the Fourier transform infrared (FT-IR) analysis and soaking-drying test results, treatment with MAN at 150°C for 4 h resulted in formation of stable crosslinks. In the second stage, MMA was used for in situ polymerization within MAN-treated wood. Field emission scanning electron microscopy observation and FT-IR analysis indicated that MMA copolymerized with MAN, and the resultant polymer filled up the lumen and is also grafted on to the cell wall. Improvement of water repellency and dimensional stability were observed in the treated samples, particularly in combined treated samples. The MAN/MMA treatment improved interaction between polymer and wood.     

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.