Electrochemical and thermal characterization of doped ceria electrolyte with lanthanum and zirconium

Nanocomposites electrolytes consisting of La³⁺ and Zr⁴⁺ doped with ceria labelled as La_0.2 Ce_0.8 O_2-δ (LDC), Zr_0.2Ce_0.8O_2-δ (ZDC) and Zr_0.2La_0.2Ce_0.6O_2-δ (ZLDC) have been synthesized via a co-precipitation route. DC conductivity was studied with a four-probe method in the range of temperature 450–650 °C and maximum conductivity was found to be 0.81 × 10^?2 S.cm^?1 (LDC) > 0.32 × 10^?2 S.cm^?1 (ZLDC) > 0.15 × 10^?2 S.cm^?1 (ZDC) at a temperature of 650 °C, respectively. Further, electric behavior of doped and co-doped ceria electrolytes was investigated by A.C electrochemical impedance spectroscopy (frequency range ~ 0.1 Hz?4 MHz). The phase/structural identification of the material prepared was studied using X-ray diffraction and found ceria to possess a cubic fluorite structure. Scanning electron microscopy (SEM) was carried out to study its morphology and particle size (~ 90–120 nm). Thermal behavior on its change in weight and length with the temperature were studied by thermogravimetric analysis (TGA) and dilatometry respectively. Furthermore, thermal expansion coefficients (TECs) of prepared electrolytes are calculated and found as follows: 13.4 × 10^?6 °C^?1, 13.6 × 10^?6 °C^?1and 15.3 × 10^?6 °C^?1 for LDC, ZDC and ZLDC, respectively, in the temperature range 150–1150 °C.     

Sulfonation of low‐density polyethylene and its impact on polymer properties

Sulfonation of polymers is of great importance for the packaging industry mainly due to its effect on the alteration of surface functionality of polymer films. In this study we customized liquid phase sulfonation of low‐density polyethylene (LDPE) swelling the polymer by using a combination of polar and nonpolar solvents. Swollen polymer was treated with sulfuric acid of varying concentrations with continuous mixing for in‐depth sulfonation of the polymer. Presence of cyclohexane and ethanol, as polar and nonpolar reagents, not only kept the batch under isothermal conditions but also homogenously influenced in‐depth functionalization of LDPE. The durability of the sulfonated polymer was determined by grinding the test samples 30 days after the reaction. Fourier transform‐infrared spectroscopy indicated presence of functional group moieties, which is also supported by increase of 5% and 1.35% in density and sulfur contents of the polymer, respectively. Contact angle measurements indicate 30° decrease in values of the sulfonated polymer which corresponds with decrease in carbon to hydrogen ratio (from 5.9 to 5.3) and increase in sulfur to carbon ratio (up to 0.0184) resulting from the sulfonation of the polymer. Differential scanning calorimetery results indicate almost linear reduction in the crystallinity of LDPE with an increase in acid concentration used for the sulfonation reaction. POLYM. ENG. SCI., 54:2522–2530, 2014. © 2013 Society of Plastics Engineers     

The Discovery of Potent Nonstructural Protein 5A (NS5A) Inhibitors with a Unique Resistance Profile—Part 2

In ongoing studies towards novel hepatitis C virus (HCV) therapeutics, inhibitors of nonstructural protein 5A (NS5A) were evaluated. Specifically, starting from previously reported lead compounds, peripheral substitution patterns of a series of biaryl‐linked pyrrolidine NS5A replication complex inhibitors were probed and structure–activity relationships were elucidated. Using molecular modelling and a supercritical fluid chromatographic (SFC) technique, intramolecular H‐bonding and peripheral functional group topology were evaluated as key determinants of activity and membrane permeability. The novel compounds exhibited retained potency as compared with the lead compounds, and also showed promising results against a panel of resistance viruses. Together, the results of the study take us a step closer towards understanding the potency of daclatasvir, a clinical candidate upon which the compounds were based, and to designing improved analogues as second‐generation antiviral agents targeting NS5A.     

Bioresorbable and degradable behaviors of PGA: Current state and future prospects

Polyglycolic acid (PGA) is a class of semicrystalline, bioresorbable polymers that have been widely used in a number of applications. No other bioresorbable materials can fully replace PGA in tissue engineering. Understanding degradation mechanisms in PGA is important for improving the efficiency and effectiveness in various fields including implantation. This review begins with a discussion on terminology of polymer degradation and hydrolytic degradation mechanism with a delineative model. This review also focus on previous degradation studies taking advantage of its fast-degrading behavior and the mechanism behind hexafluoroisopropanol (HFIP) being the sole solvent for PGA. Finally, the merits of PGA are discussed with many potential future applications along with their associated challenges.     

Activated-Carbon Nanofibers/Graphene Nanocomposites and Their Adsorption Performance Towards Carbon Dioxide

Activated-carbon nanofibers (ACNFs) provide a relatively new, modified structure of carbon-based adsorbents that have the ability to adsorb carbon dioxide due to their high specific surface area, wide distribution of porous structures, and high volume of active sites. In this study, cost-effective agricultural waste-based graphene synthesized from rice husk ashes was used as additive to enhance the ACNF properties. ACNF/graphene (gACNF) is still a relatively unexplored adsorbent. The resultant gACNF exhibited better thermal stability properties, with higher yield, larger specific surface area, and higher micropore volume. These properties are the main factors contributing to their enhanced adsorption performance towards CO₂.     

Oscillatory structure–property correlation in azelate polyols and thermoplastic polyurethanes

Azelate polyols of 2000 g mol^?1 have been successfully prepared via esterification of renewable azelaic acid with linear diols containing different number of CH₂ repeating units. Structure–property correlation of the azelate polyols had been evaluated in thermoplastic polyurethanes (TPUs). TPUs based on azelate polyols of longer chained linear diols with >4 CH₂ repeat units retained higher degrees of crystallinity associated with the polyol soft segment. The ratio of hydrogen bonded urethane in the hard segment to free urethane phase mixed with the soft segment in the TPUs showed a complex oscillating dependence with increased number of CH₂ repeating unit in the linear diols of azelate polyols. Correspondingly, static and dynamic properties of TPUs also showed the oscillatory dependence, whereby dynamic properties maximized with odd number of CH₂ repeating unit and material strength maximized with even number of CH₂ repeating unit. The results therefore can be used as guide to select appropriate azelate polyols to target specific TPU performance. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46258.     

Mechanical,thermal, and morphology properties of poly(lactic acid) plasticized with poly(ethylene glycol) and epoxidized palm oil hybrid plasticizer

Poly(lactic acid) (PLA) has received great attention recently due to its good physical and mechanical properties such as high tensile strength and modulus, good processability and biodegradability. In this study, low molecular weight poly(ethylene glycol) (PEG) and epoxidized palm oil (EPO) were used as hybrid plasticizers to improve toughness and ductility of PLA. Using the solubility parameter, a tentative evaluation of the hybrid plasticizer that could act as the most effective plasticizer for PLA has been performed and the obtained results have been corroborated with the materials physical properties. Excellent plasticizing effect was obtained by hybrid plasticizer PEG:EPO with ratio 2:1. Addition of PEG:EPO (2:1) hybrid plasticizer to PLA shows a significant improvement of 12,402%, compared to neat PLA. The improvement in flexibility and decrease in rigidity for the plasticized PLA is well evidenced by lower glass transition temperature (T_g) and tensile modulus values. In relation to the thermal stability, a decrease in thermal properties of the hybrid plasticized PLA was observed due to the volatility of the plasticizers. Scanning electron microscopy (SEM) shows that the hybrid plasticizer was turned PLA's smooth surface to fibrous structure and rough fracture surface. POLYM. ENG. SCI., 56:1169–1174, 2016. © 2016 Society of Plastics Engineers     

Modification of pristine multiwalled carbon nanotube by grafting with poly(methyl methacrylate) using benzoyl peroxide initiator

Multiwalled carbon nanotube was successfully grafted with poly(methyl methacrylate) by free radical mechanism using benzoyl peroxide initiator. The reaction was carried out in situ, where the initiator and methyl methacrylate monomer generated the polymer‐free radical that was subsequently grafted to the surface of the pristine multiwalled carbon nanotube. The multiwalled carbon nanotube grafted poly(methyl methacrylate) (MWCNT‐g‐PMMA) were characterized using Fourier transform infrared, differential scanning calorimetry, thermogravimetric analysis, ¹³ C‐solid NMR spectroscopy, X‐ray photoelectron spectroscopy, and scan electron microscopy. From the result of the characterizations, the grafting of poly(methyl methacrylate) on to multiwalled carbon nanotube was confirmed, and a percentage grafting of 41.51% weight was achieved under optimized conditions with respect to the temperature and the amount of the initiator. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43270.     

Multivariate determination of cloud point in palm oil using partial least squares and principal component regression based on FTIR spectroscopy

A rapid FTIR spectroscopic method was developed for quantitative determination of the cloud point (CP) in palm oil samples. Calibration samples were prepared by blending randomized amounts of palm olein and palm stearin to produce a wide range of CP values ranging between 8.3 and 47.9°C. Both partial least squares (PLS) and principal component regression (PCR) calibration models for predicting CP were developed by using the FTIR spectral regions from 3000 to 2800 and 1800 to 1600 cm⁻¹. The prediction capabilities of these calibration models were evaluated by comparing their standard errors of prediction (SEP) in an independent prediction set consisting of 14 palm oil samples. The optimal model based on PLS in the spectral range 1800-1600 cm⁻¹ produced lower SEP values (2.03°C) than those found with the PCR (2.31°C) method. FTIR in conjunction with PLS and PCR models was found to be a useful analytical tool for simple and rapid quantitative determination of CP in palm oil.     

An extended DEM–CFD model for char combustion in a bubbling fluidized bed combustor of inert sand

This paper proposes a transient three-phase numerical model for the simulation of multiphase flow, heat and mass transfer and combustion in a bubbling fluidized bed of inert sand. The gas phase is treated as a continuum and solved using the computational fluid dynamics (CFD) approach; the solid particles are treated as two discrete phases with different reactivity characteristics and solved on the individual particle scale using an extended discrete element model (DEM). A new char combustion submodel considering sand inhibitory effects is also developed to describe char particle combustion behavior in the fluidized bed. Two conditions, i.e. a single larger graphite particle and a batch of smaller graphite particles, are used to test the prediction capability of the model. The model is validated by comparing the predicted results with the previous measured results and conclusions in the literature in terms of bed hydrodynamics, individual particle temperature, char residence time and concentrations of the products. The effects of bed temperature, oxygen concentration and superficial velocity on char combustion behavior are also examined through model simulation. The results indicate that the proposed model provides a proximal approach to elucidate multiphase flow and combustion mechanisms in fluidized bed combustors.