Use of clay-anchored reactive modifier for the synthesis of poly (styrene-co-butyl acrylate)/clay nanocomposite via in situ AGET ATRP

Atom transfer radical polymerization using activators generated by electron transfer (AGET ATRP) was employed to synthesize well-defined poly (styrene-co-butyl acrylate)/clay nanocomposites. Dodecyltrimethylammonium bromide (DDTMAB) and Vinylbenzyltrimethylammonium chloride (VBTMAC) surfactants were used as clay modifier. The classical surfactant is used to expand the interlayer gallery of montmorillonite; however, double bond of reactive modifier participates in chain propagation process and forms clay-attached polymer chains. Subsequently synthesis of attached and free poly (styrene-co-butyl acrylate) chains and their composition was confirmed by Fourier-transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance spectroscopy (¹H NMR). Narrow distribution of nanocomposites molecular weight was confirmed by gel permeation chromatography (GPC). Partially exfoliated clay layers in the copolymer matrix were revealed by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Thermal properties of the nanocomposites were evaluated by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Thermal decomposition of the nanocomposites was hindered in the presence of nanoclay. Dynamic mechanical thermal analysis (DMTA) results show that addition of nanoclay was also resulted in enhanced storage modulus (E′) in comparison with the neat copolymer. Lower glass transition temperature of nanocomposites was displayed by DSC.     

Kinetic modeling of photoassisted-electrochemical process for degradation of an azo dye using boron-doped diamond anode and cathode with carbon nanotubes

To well describe the photoassisted-electrochemical process for treatment of the contaminated water, a new kinetic model was established based on the intrinsic reactions of the process. The kinetic model correlated apparent kinetic constants to operational parameters including applied current, initial dye concentration and flow rate. Degradation experiments were carried out with boron-doped diamond (BDD) anode and carbon nanotubes–polytetrafluoroethylene (CNTs–PTFE) cathode. The proposed kinetic model was validated by the experiments of C.I. Acid Blue 92 degradation in aqueous solution. The goodness of fitting (R² = 0.96) demonstrated that the new model could describe both the kinetics and the hydrodynamics of the photo-electrochemical system.     

Modelling and optimization of main independent parameters for biodiesel production over a Cu0.4Zn0.6Al2O4 catalyst using an RSM method

In this research, the modeling of Cu0.4Zn0.6Al2O4 catalysts performance and optimizing of esterification reactions were considered by the central composite design (RSM) response method. The main independent parameters of temperature, the ratio of alcohol to oil, the amount of catalyst and time duration have been considered for setting the esterification process. To access the maximum activity in the esterification process, the optimum conditions are estimated at 10.42 the molar ratio of alcohol to oil, 2.98 wt.% for the amount of catalyst at the temperature of 163.37 °C and within 4.15 hrs. Under these conditions, the conversion will be above 97.94%. These conditions have been applied to adjust the process of transesterification of waste cooking oil. The reusability of the Cu0.4Zn0.6Al2O4 nanocatalyst in the esterification reaction was investigated in this study. Employed statistical techniques and developed models can be employed as a useful tool for design, prediction, and optimization of the biodiesel production process with effective performance for various industrial applications. © 2021 Society of Chemical Industry (SCI).     

Novel isocyanate-based matrix resins for high temperature composite applications

Polyoxazolidone composites were prepared from polymeric isocyanate (PAPI 901) and epoxides (Epon 828 and DEN 431) in the presence of an oxazolidone-forming catalyst, triphenylantimony iodide. The effects of isocyanate to epoxide equivalent ratio, type of epoxide, and amount of fiberglass reinforcement on the composite properties were studied as well as the effects of post-curing temperature and time. Increasing the fiberglass content of the polyoxazolidone composites resulted in an improvement of the thermal and mechanical strength properties. The heat deflection temperature of all polyoxazolidones was > 250°C. The retention of the tensile strength at 150°C was excellent, ∼90% or higher. Polyoxazolidone composites based on DEN 431 at 1.2 isocyanate to epoxide equivalent ratio with 70 wt.% of fiberglass and post-cured at 150°C for 48 h exhibited the best properties. According to the results of DMA, TMA and DSC, the maximum operating temperature for polyoxazolidone composites is around 200°C. The TGA data showed that the decomposition temperature was ∼330°C.     

Combination of acid‐demineralization and enzymatic desizing of cotton fabrics by using industrial acid stable glucoamylases and α‐amylases

In this study, the possibility of simultaneous acid‐demineralization and enzymatic desizing of cotton fabric in acidic conditions (pH 2) by using industrial acid stable enzymes has been investigated. Acid‐demineralization is necessary to remove undesired cationic metals and earth alkalis. Our experiments showed that by use of a mixture of two appropriate enzymes, a glucoamylase (Multifect GA 10L) and an α‐amylase (Optisize Next) in a solution of citric acid and presence of a chelating agent, enzymatic desizing, and acid‐demineralization can be successfully carried out at the same time. Therefore, two processes of pretreatment were integrated into a single process, which can effectively reduce time and costs for textile industry.