Synthesis of modified catalyst and stabilization of CuO/NH4‐ZSM‐5 for conversion of methanol to gasoline

In this article, the catalytic conversion of methanol to gasoline range hydrocarbons has been studied over CuO/ NH₄‐ZSM‐5(3,5,7,9%) catalysts prepared via sono‐chemistry methods. In order to improve, copper oxide can be used as a booster on NH₄‐ZSM‐5 this catalyst property. Accordingly, the conversion process of Methanol to Gasoline (MTG) was conducted under a pressure of 1 atm and temperature of 400°C by a fixed‐bed reactor on copper oxide catalysts which were prepared based on synthetic NH₄‐ZSM‐5. The synthetic catalyst was investigated by such analyses as BET, XRD, FT‐IR, and SEM. Formation of copper oxide phase and proper distribution of copper oxide were proven on the basic level of using XRD analysis. BET analysis showed the reduction in catalyst level and SEM images depicted the proper distribution of particles. The present investigation is to study the effect of CuO loading on NH4‐ZSM‐5 support for conversion of methanol to gasoline range hydrocarbons. A series of CuO/ NH4‐ZSM‐5 catalysts were prepared, characterized, and experimented for their performance on methanol conversion and hydrocarbon yield.     

An innovative α‐calcium sulfate hemihydrate bioceramic as a potential bone graft substitute

The microstructural, in vitro and in vivo properties of the microwave‐synthesized samples were investigated using the optical microscope, scanning electron microscope, X‐ray diffraction, differential scanning calorimeter, contact angle goniometer, cell cytotoxicity assay, and chick chorioallantoic membrane (CAM) model in the study. When the calcium sulfate dihydrate (CSD) precursor underwent microwave irradiation treatment at temperatures between 100°C and 160°C, the crystal morphologies and crystalline structures were transformed from (tablet‐like CSD (monoclinic)) → (tablet‐like CSD (monoclinic) + long column α‐calcium sulfate hemihydrate (α‐CSH, hexagonal)) → (long column CSD (monoclinic) + short column α‐CSH (hexagonal)) → (uniform short column α‐CSH (hexagonal)). The high‐purity α‐CSH with uniform short column crystals around 10 μm in length can be synthesized at 160°C for 10 minutes and exhibits a higher hydrophilic feature in blood. Moreover, the cell cytotoxicity assay indicated that the microwave‐synthesized samples possessed well biocompatibility. In vivo results also demonstrated that the microwave‐synthesized α‐CSH not only induces angiogenesis formation but also facilitates osteogenesis. Therefore, the microwave‐synthesized α‐CSH is a promising bone graft substitute that can be applied in dental and orthopedic fields.     

Effect of polyethylenimine addition and washing on stability and electrophoretic deposition of Co3O4 nanoparticles

In this work, the parameters of cobalt oxide suspension such as conductivity, zeta potential, particle size, stability, and finally the electrophoretic behavior of particles in the absence and presence of polyethylenimine (PEI) in acetone medium were investigated. Also, the effects of washing on the stability and electrophoretic deposition of Co₃O₄ were studied. Characterization of the obtained layer by optical microscopy revealed that there was no deposition in the suspension without PEI, while a uniform layer was formed in the presence of PEI additive. Scanning electron microscopy (SEM) results confirmed the uniformity of layer obtained in acetone using PEI additive. Moreover, SEM results demonstrated that more porous microstructures were obtained at longer deposition durations. The difference in the porosity of the layers, as indicated by the SEM micrographs, is attributed to increase in the deposition time.     

Pressure‐dependent Raman modes near the cubic‐tetragonal transition in strontium titanate

The pressure dependence of the Raman frequency shifts of various Raman modes is calculated at room temperature using the volume data from the literature for the cubic‐tetragonal transition in SrTiO₃. The isothermal mode Grüneisen parameters of those Raman modes are obtained, which decrease with increasing pressure for this molecular crystal. Calculated Raman frequencies are then used to predict the damping constant and the inverse relaxation time of those Raman modes as a function of pressure by means of the pseudospin‐phonon (PS) coupled model and the energy fluctuation (EF) model to describe the cubic‐tetragonal transition in SrTiO₃. Also, the values of the activation energy are extracted for the Raman modes studied using both models (PS and EF). Our predicted damping constant and the inverse relaxation time for the Raman modes, can be compared with the experimental measurements close to the cubic‐tetragonal transition in SrTiO₃.     

Effect of phytic acid–modified layered double hydroxide on flammability and mechanical properties of intumescent flame retardant polypropylene system

Phytic acid–modified layered double hydroxide (Ph‐LDH) was synthesized via coprecipitation method and subsequently was used in polypropylene (PP) by combining with an ammonium polyphosphate (APP) via melt compounding method. The synergistic effect between APP and Ph‐LDH on the thermal stability, flammability, and mechanical properties of the resultant PP composites was investigated by thermogravimetric analysis, limiting oxygen index, vertical burning test (UL‐94), cone calorimeter tests, tensile test, and impact test. Morphologies of the chars obtained from the samples after the cone calorimeter tests were studied by scanning electron microscopy. The combination of APP and Ph‐LDH slightly influenced the impact and tensile properties of PP. Also, the synergistic effect between APP and Ph‐LDH occurred in the cone calorimeter test. Moreover, the combination of APP and Ph‐LDH produced better quality char that effectively suppressed the spread of the flame and volatile and finally extinguished the fire.     

Effects of Rheological Behavior of Viscoelastic Surfactants on Formation Damage in Carbonate Rocks

Viscoelastic surfactants (VES) are used in various oilfield applications such as matrix stimulation and enhanced oil recovery. The loss of surfactants during the propagation of VES could result in a significant reduction in the permeability of the rock (formation damage). The objective of the current work was to identify the effect of rheological behavior of the VES on the formation damage using core‐flooding experiments, nuclear magnetic resonance (NMR), and scanning electron microscopy (SEM) analysis. A combination of core‐flooding, NMR, and SEM techniques was used to quantify and identify the location of formation damage in carbonate core samples. The viscosity and storage modulus strongly depend on the nature and concentration of salts. The viscosity increased by increasing the salt concentration up to a specific point (15 wt% CaCl₂) and then starts decreasing. The VES formulations that displayed the maximum and minimum viscosities were used to identify the impact of rheological behavior on formation damage. Core‐flooding experiments were performed to assess the formation damage due to high‐viscosity and low‐viscosity VES formulations. The reduction in the permeability of carbonate rocks reaches more than 90% of the initial permeability. It was found that low‐viscosity VES caused more damage compared with high‐viscosity VES when they were used at constant concentrations. NMR and core‐flooding results revealed that the damage took place both in pore body and pore throat. However, most of the surfactant was retained at the pore throat.     

The Tunable Porous Structure of Gelatin–Bioglass Nanocomposite Scaffolds for Bone Tissue Engineering Applications: Physicochemical,Mechanical, and In Vitro Properties

Unidirectional freeze‐casting method is used to fabricate gelatin–bioglass nanoparticles (BGNPs) scaffolds. Transmission electron microscopy (TEM) images show that sol–gel prepared BGNPs are distributed throughout the scaffold with diameters of less than 10 nm. Fourier transform infrared spectroscopy (FTIR), and differential scanning calorimetric are used to evaluate the physicochemical properties of BGNPs. Scanning electron microscopy (SEM) micrographs present an oriented porous structure and a homogeneous distribution of BGNPs in the gelatin matrix. The lamellar‐type structure indicates an improvement of mechanical strength and absorption capacity of the scaffolds. Increasing the concentration of BGNPs from 0 to 50 wt% have no noticeable effect on pore orientation, but decreases porosity and pore size distribution. Increase in BGNPs content improves the compressive strength. The absorption and biodegradation rate reduces with augmentation in BGNPs concentration. Bioactivity is evaluated through apatite formation after immersion of the nanocomposites in simulated body fluid and is verified by SEM–energy‐dispersive X‐ray spectroscopy (EDS), an element map analysis, X‐ray powder diffractometer, and FTIR spectrum. SEM images and methyl thiazolyl tetrazolium assay confirm the biocompatibility of scaffolds and the supportive behavior of nanocomposites in cellular spreading. The results show that gelatin–(30 wt%)bioglass nanocomposites have incipient physicochemical and biological properties.     

Monitoring the film formation process of polystyrene/poly acrylamide (PS/PAAm) composite films annealed by IR heating

In this study, UV‐visible (UVV) technique was used to probe the evolution of optical transmission during the film formation from composites of polystyrene (PS) latex particles and poly acrylamide (PAAm) films annealed by the infrared radiative heating (IRH) and convectional heating. Activation energies corresponding to the void closure and the interdiffusion stages were calculated. It was shown that the activation energy for the void closure processes of viscous flow from the composite films decreased considerably in IRH annealing technique. It was observed that IRH heating speeds up the film formation process and the decrease the required energy. POLYM. ENG. SCI., 58:353–360, 2018. © 2017 Society of Plastics Engineers     

Biodegradable polypropylene/thermoplastic starch nanocomposites incorporating halloysite nanotubes

In this work, polypropylene/thermoplastic starch (PP/TPS) with and without halloysite nanotubes (HNTs) was prepared via melt mixing in order to obtain environmentally friendly plastics. PP‐grafted maleic anhydride (PP‐g‐MA) was used to improve the compatibility among the highly incompatible polymers. The mechanical characterization showed a reduction in the tensile properties of the polymer when TPS increased; however, HNT successfully compensated for some of the observed losses. The results from the thermogravimetric analysis (TGA) indicated that HNT is an efficient reinforcement for the thermal stability improvement. TPS caused an increase in the storage modulus (G′) and the complex viscosity (η*) which marks a change in the viscoelastic properties of the system. The scanning electron microscope (SEM) images showed the effective plasticization of starch and better dispersion of TPS in the presence of HNT. Some samples were also buried in the soil to measure their sustainability after their lifetime lapse. The results indicated that TPS improves the biodegradability of the PP/TPS system. PP considerably lowered the moisture uptake of TPS; nevertheless, HNT caused a slight increase in the moisture absorption. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45740.     

Highly effective organometallic‐mediated radical polymerization of vinyl acetate using alumina‐supported Co(acac)2 catalyst: A case study of adsorption and polymerization

An alumina support system for cobalt^(II) acetylacetonate (Co(acac)₂) catalyst was studied for the cobalt‐mediated radical polymerization (CMRP) of vinyl acetate (VAc). We report a simple but efficient technique to produce this supported catalysts through the adsorption of Co(acac)₂ on the surface of alumina particles. Moreover, kinetic and thermodynamic study of Co(acac)₂ adsorption on the alumina support were conducted and the influence of effective parameters were investigated. It was found that using alumina‐supported Co(acac)₂ for radical polymerization of VAc yields polymers with controlled molecular weight, narrow molecular weight distribution, and high purity. For the alumina‐supported CMRP, changing the polymerization mechanism and domination of termination pathway compared to degenerate transfer pathway resulted in a 2.5 times increase in polymerization rate (k_ap) and a drop in induction time while maintaining a good control of the VAc polymerization. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46057.