Polyhydroxybutyrate/chitosan/bioglass nanocomposite as a novel electrospun scaffold: fabrication and characterization

Scaffolds and their features play a central role in tissue engineering; so this study is based on the production of a series of electrospun PHB/Chitosan/nBG nanocomposite scaffolds with 9 wt% polyhydroxybutyrate, 10, 15 and 20 wt% chitosan and 7.5, 10 and 15 wt% nanobioglass (nBG). Electrospinning process was performed with optimal conditions of spinning machine including voltage of 16 kV, syringe-collector spacing of 16 cm, and output rate of 1 µl per hour. The developed phases and the formation of chemical bonds between ceramic and polymer bands were studied through XRD and FTIR analyses. The FE-SEM and TEM analyses showed uniform morphology of nanofibers and dispersion of bioglass nanoparticles in the fiber structure. The presence of 10 wt% bioglass nanoparticles and 15 wt% chitosan increased the tensile strength of fibers to 3.42 MPa, which was about four times greater than strength of control sample (pure PHB). The developed fibers were kept 28 days in SBF solution and 60 days in PBS solution to assess their bioactivity and biodegradability. The results showed that the presence of bioglass nanoparticles leads to a dramatic increase in absorption of calcium and phosphorus ions and weight loss of scaffold. The developed scaffold can be used for bone and teeth tissue engineering applications.     

Thermal decomposition kinetics of dynamically vulcanized polyamide 6–acrylonitrile butadiene rubber–halloysite nanotube nanocomposites

Thermally stable thermoplastic elastomer nanocomposites based on polyamide 6 (PA6), acrylonitrile butadiene rubber (NBR), and halloysite nanotubes (HNTs) were dynamically vulcanized, and their nonisothermal decomposition kinetics were examined. The Friedman, Kissinger–Akahira–Sunose (KAS), Ozawa–Wall–Flynn (FWO), and modified Coats–Redfern (m-CR) isoconversional models were used to obtain information about the kinetics of the thermal decomposition of PA6–NBR–HNTs in terms of the activation energy per partial mass loss monitored through thermogravimetric analyses performed at different heating rates. An erratic trend was due to the Friedman model, especially for systems having higher HNT loadings, whereas the KAS, FWO, and m-CR models revealed very similar meaningful thermal decomposition kinetics. A relatively high activation energy corroborating a reliable thermal stability was obtained by the addition of HNTs to PA6–NBR, and the resistance against decomposition was higher for systems containing more HNT. This signified the role of the HNTs as thermal stability modifiers. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47483.     

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.     

Synthesis of Molybdenum Oxide Nanohybrids as Efficient Catalysts in Oxidation of Alcohols

Novel layered materials based on molybdenum oxide have been synthesized using three amino-carboxylate ligands; terephetalic acid, p-aminobezoic acid and diaminobenzene. On the basis of X-ray diffraction, scanning electron microscopy, thermogravimetry, and infrared results, the insertion of organic ligands into the interlayer space of molybdenum oxide has been proposed. Moreover, the influence of organic guests on the oxide structure and also their catalytic performance are discussed. Furthermore, fabrication of the nanostructured molybdenum oxide is achieved by calcinations of these hybrid materials at 600 °C. Somewhat oriented nanoplatelets are viewed with different catalytic activity.     

Application of membrane separation processes in petrochemical industry: a review

In this paper a general review on different membrane processes and membrane reactors was done. As the main aim of this paper is to review the application of membrane processes in petrochemical industry, processes such as olefin/paraffin separation, light solvent separation, solvent dewaxing, phenol and aromatic recovery, dehydrogenation, oxidative coupling of methane and steam reforming of methane were discussed in detail. Besides, separation using polymer-inorganic nano composite membranes and wastewater treatment using membrane bio-reactors were reviewed.     

Preparation of the γ-Al2O3/PANI nanocomposite via enzymatic polymerization

Peroxidase-catalyzed template-guided polymerization of aniline in the presence of γ- alumina nanosheet (NS) particles have been carried out in aqueous media and γ-Al₂O₃/PANI nanocomposite was obtained. The polymerization of aniline occurred in aqueous solution in the presence of SPS (sulfonated polystyrene) as a template and SDS (sodium dodecyl sulfate) as a surfactant. Both obtained nanocomposites were comparable by SEM images. It was demonstrated that the γ-Al₂O₃ NS/PANI-SPS nanocomposite has higher conductivity and the γ-Al₂O₃ NS/PANI-SDS nanocomposite has higher void areas. The higher conductivity of γ-Al₂O₃ NS/PANI-SPS nanocomposite is attributed to the higher coated areas of γ-Al₂O₃ NS during polymerization in comparison with γ-Al₂O₃ NS/PANI-SDS which are not coated efficiently as the former. The FT-IR studies showed that the γ-Al₂O₃ NS/PANI nanocomposite was formed by interaction of the polyaniline (PANI) and γ-Al₂O₃ NS. FTIR also showed that the amount of PANI in γ-Al₂O₃ NS/PANI-SPS is more than in γ-Al₂O₃ NS/PANI-SDS. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Continuous Application of Polyglycerol‐Supported Salen in a Membrane Reactor: Asymmetric Epoxidation of 6‐Cyano‐2,2‐dimethylchromene

In the current work, suitability of hyperbranched polyglycerol as a high loading catalyst support is demonstrated. A polyglycerol‐supported manganese‐salen complex (chemzyme) is applied as a homogeneous catalyst in the epoxidation of 6‐cyano‐2,2‐dimethylchromene. The recyclability of the corresponding catalyst was investigated in repetitive batch experiments as well as a continuous operation of the reaction in an ultrafiltration membrane reactor. An enhanced stability of the catalyst in repetitive batches was observed as a result of immobilization whereby the total turnover number increased from 23 in a single batch to 80 in four repetitive batches. To enable continuous operation, a continuously operated, stirred tanked reactor (CSTR) was equipped with an ultrafiltration membrane (MPF‐50) and a retention of 98% was determined. The continuous chemzyme membrane reactor was operated over the course of 20 residence times. After approximately 12 residence times, the steady state was reached yielding 70% conversion as well as an enantiomeric excess up to 92%. A space‐time yield (sty) of 458 g L ⁻¹ d⁻¹ and a turnover frequency (TOF_reaction) of up to 18 h⁻¹ was reached in the steady state. It was determined that the total turnover number (TTN) was enhanced by a factor of 10 from 24 (batch) up to 240 for 20 residence times in CSTR operation.     

Improving of Corrosion Behavior of Al 7075 by Applied Titania–<Emphasis Type="Italic">Benzotriazole</Emphasis> Nanostructured Coating with Sol Gel Method

Nowadays, self-healing coatings display high abrasion resistance and bond strength. Application of these coatings are reckoned the most common and the most economic method for restoration and protection against corrosion by which metal structures durability is enhanced. The major role of a self-healing hybrid coating in corrosion inhibition is to supply materials for controlling types of corrosion. In this paper, titania–Benzotriazole nanostructured coating has been applied to substrate Al 7075 by using the sol–gel process and immersion method. The bonds existing in the hybrid coating, structure and morphology and coating corrosion behavior have been studied using Fourier transform infrared spectroscopy (FTIR), GIXRD, atomic force microscopy (AFM), field emission scanning electron microscopy (FESEM) and impedance electrochemical test, respectively. The obtained results are indicative of generating a homogeneous, uniform, crack-free titania–Benzotriazole nanostructured coating associated with excellent optimization of corrosion resistance at 2.8% Benzotriazole.     

Functionally-graded shape memory alloy by diffusion annealing of palladium-coated NiTi plates

Diffusion annealing of palladium-coated Ti-Ni plates was performed at temperatures ranging from 900 °C to 1,000 °C, to accomplish a compositional gradient in Ti-rich, Ti-Ni shape memory alloys. The aim of this study was to increase the transformation temperatures and transformation temperature intervals. Palladium diffusion profiles were measured by energy dispersive spectroscopy, and the corresponding approximate diffusion coefficients of the annealed specimens were calculated. The Gaussian solution of Fick’s second law for the one-dimensional lattice diffusion of a tracer was used. The transformation behavior studies were performed by differential scanning calorimetry. It was depicted that annealed specimens show longer transformation intervals compared to the bare alloy. In addition, annealed specimens showed improved shape memory properties that were attributed to the lower amount of Ti₂Ni precipitates in the diffusion layer. The shape memory behaviour of the samples was detected using micro-indentation at room temperature, followed by heating them above the austenite formation temperature to calculate the shape recovery ratio.