Environmentally friendly synthesis and photopolymerization of acrylated methyl ricinoleate for biomedical applications

In this study, we aimed to develop an efficient synthesis and photopolymerization of acrylated methyl ricinoleate (AMR) for biomedical applications. During the first step of the synthesis, methyl ricinoleate (MR) and boric acid were esterified via azeotropic distillation in toluene. Afterward, MR–boric acid ester was acrylated with acrylic acid at 165 °C via a boric acid ester acidolysis reaction. The bulk photopolymerization of AMR was performed in the presence of the photoinitiator 2,2-dimethoxy-2-phenyl acetophenone (DMPA) under 365 nm UV irradiation. Even with the use of 0.4% DMPA, a 35% monomer conversion was achieved within 30 min. Moreover, AMR, the plant-oil-based monomer, was also copolymerized with N-isopropyl acrylamide to obtain thermoresponsive hydrogels on the glass surface for biomedical applications. The synthesized materials were characterized by Fourier transform infrared (FTIR) spectroscopy, ¹H-NMR spectroscopy, and thermal characterization via thermogravimetric analysis (TGA) and differential scanning calorimetry techniques. The surfaces were characterized by FTIR and Energy Dispersive X-ray (EDS) spectroscopy. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47969.     

An agile production network enabled by reconfigurable manufacturing systems

Emergencies, and efforts to address them, create disruptions to local and global supply chains and surges in demand of emergency resources, which substantially affect global production. Reconfigurable manufacturing systems are promising solutions to improve flexibility and to reduce the effort needed to adapt supply chains and production networks to fit a perturbed environment. This paper proposes a method for coordination of reconfigurable manufacturing resources from multiple enterprises to structure ad-hoc production networks for critical products required in emergencies. Network optimization models and interaction algorithms are integrated to evolve the production network through synchronous machine-level and network-level reconfiguration driven by data.     

Rheological analysis of ceramic pastes

This paper is concerned with a number of means of characterising the rheological properties of a ceramic paste. The intrinsic flow behaviour of the paste, during upsetting, is studied experimentally by using multi coloured paste samples, as well as by a finite element numerical computation. The flow behaviour of the paste is approximated by an elasto-viscoplastic material constitutive model and implemented by using an established finite element code. The material flow properties, which are necessary for the implementation of the numerical model, were obtained using the squeeze film and hardness indentation test configurations. The flow fields generated by the simulation are shown to be a good accord with the experimental observations. The experimental procedure for selecting the material parameters which are necessary for the implementation of the numerical model is described. The accuracy of the numerical method described is also evaluated by comparing the simulation results with experimental data obtained from the net upsetting force against the imposed relative displacement behaviour and the flow visualisation of deformed coloured layers. In these respects, a comparison of the finite element model predictions and the experimental results demonstrates a good mutual agreement.     

Stability of the δ-TeO2 phase in the binary and ternary TeO2 glasses

The stability of δ-TeO₂ phase was studied in binary TeO₂–WO₃, TeO₂–CdO and ternary TeO₂–WO₃–CdO glasses. The samples were prepared by heating high purity powder mixtures of TeO₂, WO₃ and/or CdO to 800 °C in a platinum crucible with a closed lid, holding for 30 min and quenching in water bath. Differential thermal analysis (DTA), X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques were used to characterize the thermal, phase and microstructural properties of the δ-TeO₂ phase. The addition of CdO into the tellurite glasses increased the stability range of the δ-TeO₂ phase up to higher temperature values and expanded the compositional δ-TeO₂ formation range. The formation of δ-TeO₂ phase in the binary systems was observed for samples containing 5–10 mol% WO₃ and 5–15 mol% CdO. However, for the ternary TeO₂–WO₃–CdO system the formation of δ-TeO₂ phase was determined in a wider compositional range.     

Rheological and fusion behaviors of PVC micro‐ and nano‐composites evaluated from torque rheometer data

The effects of calcium carbonate (CaCO₃) particle size on the fusion and rheological behaviors of rigid poly(vinyl chloride) (PVC) composites prepared in a Haake torque rheometer were investigated by means of torque data recorded during processing. Increasing the number of particles in the same blend volume by decreasing the particle size resulted in increasing frictional forces. This increase led in turn to increased fusion torque and decreased fusion time and temperature. The power‐law‐index values of the composites increased with decreasing particle size except for 25‐nm CaCO₃. The viscosities of all composites were found to decrease with shear rate; therefore, high pseudoplasticity was observed. At a particular rotor speed, viscosity of the composites decreased with decreasing particle size except for 25‐nm CaCO₃. The overall results showed that the particle size of CaCO₃ altered the fusion characteristics and rheological behavior of PVC. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers     

Fabrication of chitosan/polyvinyl alcohol/amine modified carbon nanotube composite films for rapid chromate removal

Composite adsorbent films with amine and hydroxyl functionalities were synthesized from chitosan (CS), polyvinyl alcohol (PVA), and amine-modified carbon nanotubes (a-MWCNT) by solvent casting method. Weight proportions of CS to PVA and weight percent of a-MWCNT were optimized to achieve highest chromate removal capacity. Structural characteristics of the composites were investigated using scanning electron microscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, and thermal gravimetric analysis. Accordingly, incorporation of a-MWCNT to CS/PVA structure resulted in the generation of nanochannels, which enhanced adsorption capacity. Moreover, the composite comprising 0.4% wt. a-MWCNT provided over 99% of Cr (VI) removal from 50 mg L⁻¹ Cr (VI) solution within five minutes of contact time. Redlich–Peterson and Radke–Prausnitz isotherm models provided the highest conformity to adsorption data. Maximum chromate sorption capacity of CS/PVA/a-MWCNT composite film was determined as 134.2 mg g⁻¹ being 172% higher than that of CS/PVA. Regeneration was best achieved in 1.0 M NaOH and the composite was shown to retain at least 70% of its original capacity after five consecutive adsorption–desorption cycles.     

Ytterbium (III) oxide reinforced novel TeO2–B2O3–V2O5 glass system: Synthesis and optical,structural, physical and thermal properties

Different samples of xTeO₂.(25-y)B₂O₃.zV₂O₅.yYb₂O₃ (or TBVY) new glass material were synthesized by the classical melt-quenching method. Structural, optical, physical, and thermal analyses of the synthesized glasses were performed in addition to Monte Carlo simulation to test radiation shielding properties. The results showed that increasing ratios of Yb₂O₃ (y = 0.0, 0.5, 1.0, and 1.5 mol%) produced monotonic density values of the synthesized glasses ranging from 4.70058 g cm^?3 to 5.01038 g cm^?3. XRD and FTIR analyses were used to confirm the glass structure of all samples. Optical transmittance and absorption parameters varied almost monotonically with increasing ratios of Yb₂O₃ indicating the ability to predict and control these properties using Yb₂O₃ additive. Furthermore, simulated radiation interaction parameters, such as attenuation coefficients and half-value layer, exhibited well-behaved dependence on the concentration ratio of the Yb₂O₃ additive. This approach to glass material synthesis demonstrate the useful synergetic effect of combining structural, optical, and radiation characteristics.