Selected Physicochemical Properties of Starch Isolated from Fermented Sorghum Flour

Starch was isolated from fermented sorghum flour (24 h natural lactic acid fermentation), and water retention, starch solubility, clarity of starch pastes and freeze‐thaw stability were measured. In comparison with starch isolated from unfermented sorghum flour, fermentation increased the solubility of the starch and decreased the water retention, but it had no effect on the freeze‐thaw stability of the starch. There was no substantial difference in the starch paste clarity between the two samples. Storage of starch pastes at lower temperature (4°C) resulted in a very low clarity of starch.     

Amphiphilic Pentablock Copolymers Prepared from Pluronic and ε-Caprolactone by Enzymatic Ring Opening Polymerization

Amphiphilic copolymers are appealing materials because of their interesting architecture and tunable properties. In view of their application in the biomedical field, the preparation of these materials should avoid the use of toxic compounds as catalysts. Therefore, enzymatic catalysis is a suitable alternative to common synthetic routes. Pentablock copolymers (CUC) were synthesized with high yields by ring-opening polymerization of ε-caprolactone (ε-CL) initiated by Pluronic (EPE) and catalyzed by Candida antarctica lipase B enzyme. The variables to study the structure–property relationship were EPEs’ molecular weight and molar ratios between ε-CL monomer and EPE macro-initiator (M/In). The obtained copolymers were chemically characterized, the molecular weight determined, and morphologies evaluated. The results suggest an interaction between the reaction time and M/In variables. There was a correlation between the differential scanning calorimetry data with those of X-ray diffraction (WAXD). The length of the central block of CUC copolymers may have an important role in the crystal formation. WAXD analyses indicated that a micro-phase separation takes place in all the prepared copolymers. Preliminary cytotoxicity experiments on the extracts of the polymer confirmed that these materials are nontoxic.     

Effect of Gamma Rays on Starch Extracted from Irradiated Wheat Flour

Irradiated starch was more retrograded than the unirradiated samples. The amylose fractions were increased on the expence of the amylopectin fractions of starch under the influence of gamma rays. Oxidation of starch with periodate ions was enhanced by gamma irradiation as indicated by the formation of greater amounts of formic acid in the irradiated samples. This result indicated that destruction in amylopectin had occured and formed small branched fragments. The decrease in intrinsic viscosity due to radiation, showed a straight line relation, when plotted versus irradiation doses, with a slope of 5.2 × 10⁻⁷. This indicates that a specific slope could be obtained which characterized gamma ray doses on wheat flour.     

Review on zirconate-cerate-based electrolytes for proton-conducting solid oxide fuel cell

The performance of low-to-intermediate temperature (400–800?°C) solid oxide fuel cells (SOFCs) depends on the properties of electrolyte used. SOFC performance can be enhanced by replacing electrolyte materials from conventional oxide ion (O^2-) conductors with proton (H⁺) conductors because H⁺ conductors have higher ionic conductivity and theoretical electrical efficiency than O^2- conductors within the target temperature range. Electrolytes based on cerate and/or zirconate have been proposed as potential H⁺ conductors. Cerate-based electrolytes have the highest H⁺ conductivity, but they are chemically and thermally unstable during redox cycles, whereas zirconate-based electrolytes exhibit the opposite properties. Thus, tailoring the properties of cerate and/or zirconate electrolytes by doping with rare-earth metals has become a main concern for many researchers to further improve the ionic conductivity and stability of electrolytes. This article provides an overview on the properties of four types of cerate and/or zirconate electrolytes including cerate-based, zirconate-based, single-doped cerate–zirconate and hybrid-doped cerate–zirconate. The properties of the proton electrolytes such as ionic conductivity, chemical stability and sinterability are also systematically discussed. This review further provides a summary of the performance of SOFCs operated with cerate and/or zirconate proton conductors and the actual potential of these materials as alternative electrolytes for proton-conducting SOFC application.     

Al2O3/Yttria‐Stabilized Zirconia Hollow‐Fiber Membrane Incorporated with Iron Oxide for Pb(II) Removal

Removal by absorptive ceramic membranes can simultaneously absorb and separate metal ions from water. Alumina/yttria‐stabilized zirconia (Al₂O₃/YSZ) hollow‐fiber membranes, fabricated using phase inversion and sintering process, were deposited with iron oxide by an in‐situ hydrothermal process. The results showed that α‐Fe₂O₃ was produced and incorporated across the membranes. A reduction in flux was recorded with the deposition of α‐Fe₂O_3. However, it improved the adsorption capacity for heavy metal adsorption. The adsorption‐separation test demonstrated that the optimized membrane is able to completely remove Pb(II) ions after two hours.     

Colour and ergonomics: On the selection of a “colour of the year”

The key role of colour in ergonomics has been emphasized by a number of researchers and design professionals. Although several research studies have been published regarding the use of colour in ergonomics, there are still some areas that need to be considered. The issue of deciding a “colour of the year” is an example, which represents a new challenge for researchers in the field of ergonomics. This is of particular interest considering the fact that the nature of research on the selection of a “colour of the year” is generally based on user experience. This paper argues that ergonomics should play a more prominent role in this field to ensure better user experience and performance. This paper highlights specific areas that need further study and development.     

Chemically induced graft copolymerization of 4-vinyl pyridine onto carboxymethyl chitosan

A novel super absorbent polymer was prepared by graft copolymerization of 4-vinyl pyridine (4VP) onto the chains of carboxymethyl chitosan in aqueous solution using potassium persulphate (KPS) as initiator. The effect of monomer and initiator concentration, reaction temperature, and time on the grafting yield has been investigated. The maximum grafting yield was achieved at [KPS] = 4 × 10⁻² mol/L, [M] = 2.5 mol/L at reaction temperature = 60 °C within reaction time = 3 h. The molecular structure of the graft copolymer was confirmed by FTIR, surface morphology before and after the polymerization was examined by SEM. Different analyses were done for the graft copolymer such as X-ray diffraction, solubility tests, and thermal analysis. Different applications were done on the graft copolymer such as swell ability in different pH solutions, dye, and metal uptake.     

Microstructure and phase composition of cordierite-based co-clinker

The aim of this work is to study the effect of phase composition and microstructure of cordierite-based co-clinkers on the electrical properties and coefficient of thermal expansion of cordierite briquettes. To achieve this aim talc and kaolinite samples were collected from quarries in the Egyptian desert. The samples are characterized using XRD, XRF, polarized light, cathodoluminescence and SEM microscopy attached with EDAX, in addition to X-ray micro-computed tomography (3D- µXCT). The electrical properties and coefficient of thermal expansion of the cordierite briquettes are determined using HiTESTER instrument and automatic Netzsch DIL402 PC dilatometer, respectively.Five talc-based batches were shaped and fired in the temperature range 1000–1350 °C for 2 h. The microstructural and physical characteristics of the resulted cordierite-based co-clinkers depend mainly on the viscosity of the liquid phase developed during firing. The microchemistry of the cordierite briquettes confirms their enrichment of both cordierite and ferroan-cordierite crystallized directly from locally developed melts. The dielectric constant and loss factor values for cordierite briquettes allow their possible use as insulator components in electronic applications.     

Oligomeric Composition of Polyols From Fatty Acid Methyl Ester: The Effect of Ring‐Opening Reactants of Epoxide Groups

Commercial availability of fatty acid methyl ester (FAME) from palm oil targeted for biodiesel offers a good feedstock for the production of structurally well‐defined polyols for polyurethane applications. The effect of molecular weight (MW), odd and even carbon numbers, and the linear and branched structure reactants used in the ring‐opening reaction of epoxidized fatty acid methyl ester (E‐FAME) on the properties of polyols was investigated. Conversions of E‐FAME to PolyFAME polyols were confirmed by Fourier transform infrared analysis, oxirane oxygen content, and hydroxyl number. Gel permeation chromatography (GPC) calibrated against polyether polyols as a standard and vapor pressure osmometry were used for MW determination. GPC chromatograms of PolyFAME polyols clearly demonstrated the formation of oligomers during ring‐opening reactions. MW, and odd and even carbon numbers in a structure of linear diols and branched diol used in the syntheses of PolyFAME polyols did not have an effect on crystallinity, glass transition, or melt temperatures measured using Differential scanning calorimetry (DSC). PolyFAME polyols ring‐opened with water, methanol, and 1,2‐propanediol contained secondary hydroxyl groups, whereas PolyFAME polyols ring‐opened with linear diols contained a mixture of primary and secondary hydroxyl groups. It was found that the concentration of primary hydroxyl groups increased significantly by increasing the number of carbons from C2 to C3 in the linear diols. The viscosity of PolyFAME polyols also increased with the MW of linear diols used in the E‐FAME ring‐opening reaction. These findings would be beneficial for formulators in choosing the most cost effective polyols for polyurethane formulations.     

Comparison of prolonged antibacterial activity and release profile of propolis‐incorporated PVA nanofibrous mat,microfibrous mat,and film

Propolis as a natural antibacterial agent was incorporated into the poly(vinyl alcohol) (PVA) in different forms of nanofiber, microfiber, and film. The successful fabrication of uniform nanofibers with 85–314 nm diameters and microfibers with 2.02 μm diameter was proved by scanning electron microscopy. Structural analysis by Fourier transform infrared spectroscopy and X‐ray diffraction and swelling properties confirmed the formation PVA hydrogel and its H‐bonding to the propolis. Evaluation and comparison of antimicrobial properties of produced samples against Staphylococcus aureus strains revealed that nanofiber mat with 19 mm inhibition zone has 11.76 and 26.67% higher efficiency against bacteria than microfiber mat and film with 17 and 15 mm inhibition zone, respectively. Nanofibrous mat showed sustained release during 96 h by maintaining full antibacterial activity up to 51 h which is of great importance in burn wounds. These results confirm the advanced performance of natural propolis in the form of nanofiber substrate as wound dressing. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45794.