AlBr3 impact on the thermal degradation of P(S-co-MMA): a study performed by contemporary techniques

Pyrolysis of copolymer, [P(S-co-MMA)], in the presence of AlBr₃ was inspected in an inert atmosphere. Five different proportions (copolymer/additive) were chosen. Films were cast from common solvent. It was noticed that copolymer showed more stability on the basis of T _0, however, regions of stability were also observed for the blends. Copolymer showed T ₀ at 260?°C, whereas blends started degrading around 70?°C. T _max was the same for the copolymer and the blends. Low-temperature decompositions of blends were attributed to the generation of free radicals (Br^?) and the zones of stabilizations were assigned to the formation of a ??complex type?? structure between Al and the carbonyl oxygens of MMA units. Degradation products were collected and identified employing Py-GC?CMS technique. Intermediates (solid) at different temperatures (300, 350 and 400?°C) were examined through FTIR spectroscopy. In the light of gathered data, a degradation mechanism was proposed. New products were encountered, viz., bromobenzene, ??brominated?? anhydride ring, etc., which established the chemical interactions between the constituents of the blends, i.e., copolymer and additive. Anhydride rings were absent when poly (methyl methacrylate) was pyrolyzed in the presence of AlBr₃. Oligomers of styrene were not found hinting at the involvement of additive in ??targeting?? the degrading styrene units. The blends indicate 2?C7% residue of original mass; the additive exhibits 9% while the copolymer does not leave residue at the completion of the TG run. The presence of char in the residues of blends suggests that the additive imparts stability to the copolymer. Horizontal burning rate was lowest (6 times less than that of neat copolymer) for [P(S-co-MMA):AlBr₃, 87.5:12.5%], thereby revealing the efficiency of the additive as thermal stabilizer. The highest activation energy was calculated for the copolymer (169.46?kJ/mol) and the range of this parameter for the blends was found from 52.72 to 27.14?kJ/mol.     

Effect of TiO2 nanoparticle on rheological behavior of poly(vinyl alcohol) solution

In recent years, addition of nanoparticles to fluids and polymers has been used as a way of modifying rheological properties. Poly(vinyl alcohol) (PVA) and titanium dioxide (TiO₂) nanoparticles aqueous composite nanofluids were prepared through the use of ultrasonic vibration. In fact, ultrasonic vibration is an advantageous method for nanoparticle dispersion. The preparation method prevents reduction of the polymer's molecular weight. TiO₂ nanoparticles with different concentrations were employed to investigate the rheological characteristics of composite nanofluids. Rheological characteristics of base fluids and composite nanofluids were measured at different temperatures. Based on the results, all composite nanofluids, as well as base fluids, exhibited non‐Newtonian behavior and rheological characteristics of composite nanofluids, following the Herschel‐Bulkley model. In addition, model parameters are functions of temperature, PVA, and TiO₂ nanoparticle concentrations. Also, two‐way interactions among temperature, PVA, and TiO₂ nanoparticle concentrations affect flow index and consistency index of the Herschel‐Bulkley model. J. VINYL ADDIT. TECHNOL., 23:234–240, 2017. © 2015 Society of Plastics Engineers     

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.     

Recent advancements in bioreactions of cellular and cell-free systems: A study of bacterial cellulose as a model

Conventional approaches of regulating natural biochemical and biological processes are greatly hampered by the complexity of natural systems. Therefore, current biotechnological research is focused on improving biological systems and processes using advanced technologies such as genetic and metabolic engineering. These technologies, which employ principles of synthetic and systems biology, are greatly motivated by the diversity of living organisms to improve biological processes and allow the manipulation and reprogramming of target bioreactions and cellular systems. This review describes recent developments in cell biology, as well as genetic and metabolic engineering, and their role in enhancing biological processes. In particular, we illustrate recent advancements in genetic and metabolic engineering with respect to the production of bacterial cellulose (BC) using the model systems Gluconacetobacter xylinum and Gluconacetobacter hansenii. Besides, the cell-free enzyme system, representing the latest engineering strategies, has been comprehensively described. The content covered in the current review will lead readers to get an insight into developing novel metabolic pathways and engineering novel strains for enhanced production of BC and other bioproducts formation.     

Rheological and mechanical properties of composites made from wood flour and recycled LDPE/HDPE blend

The effect of compounding method is studied with respect to the rheological behavior and mechanical properties of composites made of wood flour and a blend of two main components of plastics waste in municipal solid waste, low-density polyethylene (LDPE) and high-density polyethylene (HDPE). The effects of recycling process on the rheological behavior of LDPE and HDPE blends were investigated. Initially, samples of virgin LDPE and HDPE were thermo-mechanically degraded twice under controlled conditions in an extruder. The recycled materials and wood flour were then compounded by two different mixing methods: simultaneous mixing of all components and pre-mixing, including the blending of polymers in molten state, grinding and subsequent compounding with wood flour. The rheological and mechanical properties of the LDPE/HDPE blend and resultant composites were determined. The results showed that recycling increased the complex viscosity of the LDPE/HDPE blend and it exhibited miscible behavior in a molten state. Rheological testing indicated that the complex viscosity and storage modulus of the composites made by pre-mixing method were higher than that made by the simultaneous method. The results also showed that melt pre-mixing of the polymeric matrix (recycled LDPE and HDPE) improved the mechanical properties of the wood–plastic composites.     

Effect of apple cider vinegar agent on the microstructure,phase evolution,and magnetic properties of CoFe2O4 magnetic nanoparticles

In the present study, spinel structure CoFe₂O₄ nanoparticles were successfully synthesized by the sol-gel auto-combustion technique. The effect of apple cider vinegar (ACV) addition as an organic biocompatible agent on the size, morphology, and magnetic properties of CoFe₂O₄ nanoparticles was investigated in detail. The phase evolution, particle size, and lattice parameter changes of the synthesized phase have been estimated by using Rietveld structure refinement analysis of X-ray powder diffraction data. Also, Fourier transform infrared spectra (FT-IR) of the samples verified the presence of two expected bands correspond to tetrahedral and octahedral metal-oxygen complexes within the spinel structure. Furthermore, microstructural observations revealed that ultrafine particles have a semi-spherical morphology. It was shown that the particles size decreased from ~45 to ~17 nm with an increase in the amount of ACV. Magnetic properties were carried out by vibrating sample magnetometer (VSM) at room temperature. Both the saturation magnetization (M_s) and coercivity (H_c) were found to be significantly dependent on the crystallite size and the amount of ACV.     

The Ablation and Oxidation Behaviors of SiC Coatings on Graphite Prepared by Slurry Sintering and Pack Cementation

SiC coatings were generated on graphite using slurry sintering (SS) and pack cementation (PC). The samples’ ablation features were assessed by an oxyacetylene torch. The rates of mass ablation of the PC–SiC and SS–SiC coatings were approximated 2.17?×?10^?3 and 9.52?×?10^?3 g s^?1, respectively, decreased by 84.1 and 29.6% compared to the uncoated samples. It was mainly attributed to the formation of a SiO₂ layer on the surface. The continuous SiO₂ molten film formed via the PC–SiC oxidation generates a sealing mechanism which can be an obstacle against the oxygen diffusion and hinder more ablation. This is while discontinuous SiO₂ film formed from the thin SS–SiC cannot protect the graphite effectively. The non-isothermal oxidation test shows that without the SiC coating, the sample weight is lost largely from 25 to 1500 °C, and its weight loss was 2.2% after the TGA. However, after coating, the samples possessed excellent oxidation protection and weight losses of SS–SiC and PC–SiC coatings are down to 1.3 and 0.6%, respectively. The more oxidation of the graphite substrate occurred due to the formation of macrocracks in the coating during the TGA and also the formation of holes on SiO₂ glass layer owing to release of CO or CO₂.     

Characterization and formation mechanism of nanocrystalline W–Al alloy prepared by mechanical alloying

Tungsten and aluminum elemental powders with composition W–20 wt.% Al were mechanical alloyed in high energy planetary ball mill. Structural and morphological changes of powder particles after different milling times were studied by X-ray diffractometer, scanning electron microscopy and microhardness measurements. Mechanical alloying of this system led to the formation of W–Al alloy as a result of formation of W/Al layered microstructure having faceted interface between layers. This alloy indicated high microhardness value of about 570 Hv.     

Influence of Ultrasonic Waves on the Processing of Cotton with Cationic Softener

In recent years, the textile industry has been forced to develop new technologies to reduce energy and water consumption. The use of ultrasound in textile wet processing is one solution to this problem. The aim of this work was to investigate the effects of ultrasonic energy on the processing of cotton with a cationic softener. For this purpose, cotton fabric was treated with a fatty acid amide derivative cationic softener in water using ultrasonic energy during treatment. The physical properties of the fabrics treated under different conditions are discussed. The results show that the treatment of fabrics with softeners in an ultrasound bath is more effective compared to conventional methods and that it enhances the physical properties of the cotton.     

通过双级固溶热处理制备新型高强Al−10.5Si−3.4Cu−0.2Mg合金

通过析出硬化提高Al?Si?Cu合金的力学性能.这些合金对时效硬化的反应非常缓慢.为了解决这一问题,在Al?10.5Si?3.4Cu合金中分别加入0.2％、0.4％和0.7％(质量分数)的镁.该新型合金在固溶处理阶段经过两种不同的析出硬化过程.结果表明,添加不同含量的镁可加速该合金对时效处理的响应,提高其硬度和强度.双...