Synthesis of high molecular weight aromatic polyesters via integrated alternating ring-opening copolymerization and chain extension methods

Due to their good mechanical properties, high molecular weight polyesters (PEs) are highly desirable for a wide range of applications especially in the packaging industry. However, the synthesis of high molecular weight polymers by energy efficient methods is difficult. In this study, a series of semi-aromatic PEs were synthesized via the alternating ring-opening copolymerization (ROCOP) of phthalic anhydride (PA) and cyclohexene oxide (CHO) using a salen chromium(III) complex as a catalyst and 4-(dimethylamino)pyridine as a cocatalyst. By varying the molar ratios between CHO and PA, PEs of different molecular weights were obtained. Hexamethylene diisocyanate was used as a chain extender that further increased the molecular weights of these PEs. These chain extended aromatic polyesters (PE-Xs) showed significant improvement in the glass transition temperature (T_g) values. Thus, integration of ROCOP with the chain extension method can be used as an effective strategy to prepare high molecular weight PEs with improved thermal stabilities and enhanced mechanical properties. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47200.     

Facile modification of polysulfone hollow-fiber membranes via the incorporation of well-dispersed iron oxide nanoparticles for protein purification

Protein existence in wastewater is an important issue in wastewater management because proteins are generally present as contaminants and foulants. Hence, in this study, we focused on designing a polysulfone (PSf) hollow-fiber membrane embedded with hydrophilic iron oxide nanoparticles (IONPs) for protein purification by means of ultrafiltration. Before membrane fabrication, the dispersion stability of the IONPs was enhanced by the addition of a stabilizer, namely, citric acid (CA). Next, PSf–IONP–CA nanocomposite hollow-fiber membranes were prepared via a dry–wet spinning process and then characterized in terms of their hydrophilicity and morphology. Ultrafiltration and adsorption experiments were then conducted with bovine serum albumin as a model protein. The results that an IONP/CA weight ratio of 1:20 contributed to the most stable IONP dispersion. It was also revealed that the membrane incorporated with IONP–CA at a weight ratio of 1:20 exhibited the highest pure water permeability (58.6 L m⁻² h⁻¹ bar⁻¹) and protein rejection (98.5%) while maintaining a low protein adsorption (3.3 μg/cm²). The addition of well-dispersed IONPs enhanced the separation features of the PSf hollow-fiber membrane for protein purification. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47502.     

Novel sulfonated multi-walled carbon nanotubes filled chitosan composite membrane for fuel-cell applications

In the present study, multi-walled carbon nanotubes (MWCNTs) were sulfonated by 1,3-propane sultone and distillation–precipitation polymerization, respectively, and then incorporated into chitosan (CS) to prepare CS/MWCNTs composite membranes for fuel cell applications. CS/MWCNTs membranes show better thermal and mechanical stability than pure CS membrane due to the strong electrostatic interaction between the  SO₃H groups of MWCNTs and the  NH₂ groups of CS, which can restrict the mobility of CS chain. The sulfonated MWCNTs provide efficient proton hopping sites ( SO₃H,  SO₃⁻ …. ₃⁺HN ), thereby resulting in the formation of continuous proton conducting channels. The composite membranes with 5 wt % of MWCNTs modified by two different ways show a proton conductivity of 0.026 and 0.025 S·cm⁻¹, respectively. In conclusion, CS/MWCNTs membrane is a promising proton exchange membrane for fuel-cell applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47603.     

Easy,operable ionic polymer metal composite actuator based on a platinum‐coated sulfonated poly(vinyl alcohol)–polyaniline composite membrane

In this study, an electric‐stimulus‐responsive bending actuator based on a platinum (Pt)‐coated sulfonated poly(vinyl alcohol) (SPVA)–polyaniline (PANI) composite membrane was developed. The SPVA–PANI membrane was prepared by a solution casting method; it showed good electrochemical properties and an adequate ion‐exchange capacity of 1.6 mequiv/g of dry membrane. The water uptake by the membrane with 4 h of immersion time at 45 °C was found to be 425%. The SPVA–PANI composite membrane based ionic polymer metal composite (IPMC) actuator prepared by the coating of Pt metal layers on both sides of the membrane by an electroless plating process showed a good proton conductivity of 1.75 × 10^?3 S/cm. The smooth and uniform coating of Pt on both surfaces of the membrane, as indicated by scanning electron micrographs, seemed to be responsible for the slow water loss that is necessary for the long life of an IPMC actuator. The maximum water loss was 48% at 6 V for 12 min. This indicated the better performance of the IPMC membrane when an electric potential was applied. According to electromechanical characterization, the maximum tip displacement was 14.5 mm at 5.25 V. A multifinger IPMC membrane based microgripping system was developed, and it showed potential for microrobotics application. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43787.     

A novel solvent-impregnated resin containing 3-hydroxy-2-naphthoic acid for stepwise extraction of Th(IV) and U(VI) over other coexistence ions

A new solvent-impregnated resin (SIR) was constructed using Amberlite XAD-2 and 3-hydroxy-2-naphthoic acid (3H2NA). The SIR was applied for stepwise extraction of Th(IV) and U(VI) from the coexistence ions dissolved in aqueous media at pHs of 3.0 and 7.0, respectively. The U(VI) and Th(IV) ions adsorbed on the minicolumn were consecutively eluted with 0.5 M and 4 M HCl solutions. They were then measured by Arsenazo III at their maximum absorption wavelengths. The characteristic parameters for the successful separation of these ions from the aqueous media were investigated. The SIR showed excellent reproducibility during the 800 subsequent extraction cycles.     

Measurements of Stress Intensity Factors of an Interface Crack Under Mixed Mode Loading

The optical method of caustics has been utilised to measure both the stress intensity factor for a crack lying along the interface of an aluminium/epoxy bimaterial specimen, and the mode mixity arising from the difference in the elastic properties across the interface. Measurements were carried out by using a novel modification to the method whereby caustics are produced and measured from both sides of the specimen, so compensating automatically for the distortion induced in the specimen due to misaligned loading fixtures. A flat reflective surface across the interface was obtained by adhering a reflective coating to the specimen. Verification that this coating does not affect measurement accuracy was obtained by comparing stress intensity factors measured from coated and uncoated monolithic aluminium specimens where good agreement was found to exist between both measurements.     

Use of a selective extractant-impregnated resin for removal of Pb(II) ion from waters and wastewaters: Kinetics,equilibrium and thermodynamic study

Adsorption of Pb(II) ion by a novel extractant-impregnated resin, EIR, was studied as a function of various experimental parameters using batch adsorption experiments. The new EIR was prepared by impregnating gallocyanine (GCN) onto Amberlite XAD-16 resin beads. The EIR was characterized by nitrogen analysis and SEM micrographs. The new EIR showed excellent selectivity factor values (α) for Pb(II) adsorption respect to other metal ions. The effects of some chemical and physical variables were evaluated and the optimum conditions were found for Pb(II) removal from aqueous solutions. The equilibrium adsorption isotherm was fitted with the Langmuir adsorption model. The maximum adsorption capacity (q_max) of EIR for Pb(II) ions was found to be 367.92 mg g⁻¹. The kinetic studies showed that the intra-particle diffusion is the rate-controlling step. Also, the intra-particle diffusion coefficients, D_ip values, were of the order of 10⁻¹² m² s⁻¹. The values of enthalpy (ΔH°) were positive, which confirms the endothermic nature of adsorption process. Also, the positive entropy changes (ΔS°) were showed that the randomness increased along with the adsorption process. In addition, the obtained negative values of Gibbs free energy (ΔG°) indicated feasible and spontaneous nature of the adsorption process at different temperatures. The new adsorbent was very stable so that it can be successfully used for many consecutive cycles without significant loss in its adsorption capacity.     

Evaluation of Nitrogen Fixing Enzyme Activities in Response to Pyrene Bioremediation Efficacy by Defined Artificial Microalgal-Bacterial Consortium of Gujarat,India

This study was carried out to investigate the response and relationship between nitrogen fixing enzymes during the remediation of different concentrations of high molecular weight four rings Polynuclear Aromatic Hydrocarbon (PAH) Pyrene by microalgae Synechocystis sp. (cyanobacteria) with artificial developed indigenous bacterial consortium. One axenic microalgal culture of Synechocystis sp. and two pyrene degrading indigenous bacteria with efficient removal capabilities viz. Pseudomonas indoxyladons and Bacillus benzoevorans isolated from crude oil polluted site and common industrial effluent canal were used to construct the consortium. The effect of pyrene on algal growth in terms of chlorophyll-a was measured and it was found that in the presence of bacteria, the growth and bioremediation capacity of Synechocystis sp. raised tremendously, whereas Synechocystis sp. monoculture exhibited concentration dependent decrease. Moreover, the nitrogen fixing enzymes; nitrate reductase (NR), glutamine synthetase (GS), and succinate dehydrogenase (SDH) showed chronological decrease by 93%, 90%, and 98%, respectively. Increased Bioremediation of pyrene by consortium JPNKA7B2 (Mix culture of Synechocystis sp., Pseudomonas indoxyladons, and Bacillus benzoevorans) was eliminated at 94.1% in 50 mg/L, which indirectly retarded the nitrogen fixing enzymes – NR, GS, and SDH. However, Synechocystis sp. monoculture could remediate up to 36% at 1.5 mg/L after 16 days of incubation.