A comparative study of the effects of three galactomannans on the functionality of extruded pea–rice blends

The present study evaluated the effects of three galactomannans on the physical and nutritional characteristics, and sensory acceptability of pea–rice based extruded products, targeted as nutritional snacks. A base blend of 70:30 pea and rice fortified with guar gum (GG), locust bean gum (LBG) and fenugreek gum (FG), at 5%, 10%, 15% and 20%, was extruded at pre-determined optimum processing conditions. All three gums resulted in good expanded products. Increasing the inclusion levels of gums, however, had no effect (P > 0.05) on the degree of expansion. Addition of 5% GG and LBG reduced (P < 0.05) the hardness, while the inclusion of GG and LBG at levels higher than 5%, and all inclusion levels of FG, increased (P < 0.05) the hardness of extruded products. Relative to other treatments, FG produced extrudates that were harder and crispier. The mean scores of sensory evaluation indicated that all products containing gums up to 15% were within the acceptable range. Extrusion increased (P < 0.001) the soluble fibre content and decreased the insoluble fraction; the magnitude of these changes were greater in GG and FG. The addition of 15% gums in the pea–rice blend reduced (P < 0.05) the glycaemic index to less than 55. Overall, the data suggest that all three galactomannans could be incorporated up to 15% in a pea–rice blend to develop nutritious, organoleptically acceptable, extruded snack products with low glycaemic index.     

High Electrical and Thermal Conductivity Cast Al-Fe-Mg-Si Alloys with Ni Additions

Metallurgical and Materials Transactions A - Aluminum alloys with transition metals Fe and Ni show potential to form the basis for castable alloys with high electrical and thermal conductivity for...     

Statistical method‐based calibration and validation of a solid oxide fuel cell model

A 2‐stage model validation strategy for the previously developed solid oxide fuel cell model using the data from custom‐designed experiments is presented. The strategy is based on the identification of model structural and parametric errors. In the preliminary validation, the causes that can result in the voltage error during changing temperature and fuel flow rate conditions are analysed. It is identified that the convection heat transfer process contributes significantly towards the cell performance in a temperature controlled test environment. Rectification of this error results in the reduction of the maximum voltage error from 14% to 0.5%. Graphical methods for data visualisation are utilised to examine goodness of fit of the model. Input sensitivity analysis reveals that the air flow rate has negligible influence on the output quantities of current density, fuel utilisation, and cell temperature owing to temperature‐controlled conditions of the test. Parameter sensitivity analysis through the elementary effects method reveals that most of the electrochemical parameters in general and the activation energies in particular have dominant effects on the considered system outputs. Model validation is carried out through a classical statistical method of hypothesis testing by using the parameter uncertainty information obtained through nonlinear least squares fitting. The efficacy of the model validation strategy is demonstrated through the model acceptance with 8% maximum error in cell current.     

Mapping fluorophore distributions in three dimensions by quantitative multiple angle-total internal reflection fluorescence microscopy

The decay of evanescent field intensity beyond a dielectric interface depends upon beam incident angle, enabling the 3-d distribution of fluorophores to be deduced from total internal reflection fluorescence microscopy (TIRFM) images obtained at multiple incident angles. Instrumentation was constructed for computer-automated multiple angle-TIRFM (MA-TIRFM) using a right angle F2 glass prism (n(r) 1.632) to create the dielectric interface. A laser beam (488 nm) was attenuated by an acoustooptic modulator and directed onto a specified spot on the prism surface. Beam incident angle was set using three microstepper motors controlling two rotatable mirrors and a rotatable optical flat. TIRFM images were acquired by a cooled CCD camera in approximately 0.5 degree steps for >15 incident angles starting from the critical angle. For cell studies, cells were grown directly on the glass prisms (without refractive index-matching fluid) and positioned in the optical path. Images of the samples were acquired at multiple angles, and corrected for angle-dependent evanescent field intensity using "reference" images acquired with a fluorophore solution replacing the sample. A theory was developed to compute fluorophore z-distribution by inverse Laplace transform of angle-resolved intensity functions. The theory included analysis of multiple layers of different refractive index for cell studies, and the anisotropic emission from fluorophores near a dielectric interface. Instrument performance was validated by mapping the thickness of a film of dihexyloxacarbocyanine in DMSO/water (n(r) 1.463) between the F2 glass prism and a plano-convex silica lens (458 mm radius, n(r) 1.463); the MA-TIRFM map accurately reproduced the lens spherical surface. MA-TIRFM was used to compare with nanometer z-resolution the geometry of cell-substrate contact for BCECF-labeled 3T3 fibroblasts versus MDCK epithelial cells. These studies establish MA-TIRFM for measurement of submicroscopic distances between fluorescent probes and cell membranes.     

Effect of polymer composition on performance properties of maleate-vinyl ether donor-acceptor UV-curable systems

The effect of unsaturated polyester backbone composition on the properties of donor-acceptor-UV-cured coatings was explored. The polyesters were designed with similar molecular weights and levels of unsaturation, but with otherwise widely varying backbone compositions. UV-curable coatings were formulated with stoichiometric levels of triethylenglycol divinyl ether and a photoinitiator. The resulting coatings had a broad range of properties, which were found to correlate with the properties and compositions of the polyester backbone polymers. A relatively flexible backbone resulted in lower glass transition temperatures (T_g). The polymer T_g was found to influence the conversion of double bonds achieved during UV curing. Reaction kinetics were evaluated for the coating systems and the results confirmed that the T_g of the systems influenced the double bond conversion. Thermal stability and König pendulum hardness were also found to vary with the backbone composition of the constituent polyester.     

Synthesis and properties of poly ether nitrile sulfone copolymers with pendant methyl groups

Poly ether nitrile and poly ether nitrile sulfone copolymers with pendant methyl groups were prepared by the nucleophilic substitution reaction of 2,6′‐dichlorobenzonitrile with methyl hydroquinone and with varying mole proportions of methyl hydroquinone and 4,4′dihydroxydiphenylsulfone using N‐methyl pyrrolidone as solvent in the presence of anhydrous K₂CO₃. The polymers were characterized by different physicochemical techniques. Copolymer composition was determined using FTIR technique. Thermogravimetric data reveals that all the polymers were stable up to 420°C with a char yield above 40% at 900°C in N₂ atmosphere. The glass transition temperature was found to increase and the activation energy and inherent viscosities were found to decrease with increase in concentration of the 4,4′‐dihydroxydiphenylsulfone units in the polymer. Trimerization reactions are found to be favorable with increase in concentration of methyl hydroquinone units in the polymer. Crystallinity of the polymer was also studied using wide angle X‐ray diffraction. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1303–1309, 2006     

New powellite type oxides in Ca–R–Nb–Mo–O system (R = Y, La, Nd, Sm or Bi)—Their synthesis, structure and dielectric properties

New complex oxides having powellite (CaMoO₄) type structure in the Ca–R–Nb–Mo–O system (R = Y, La, Nd, Sm or Bi) were prepared employing the method of solid state reaction between the component oxides at high temperature (1000–1100 °C). The new compounds, CaRNbMoO₈ (R = Y, La, Nd, Sm, Bi) are colorless and electrical insulators. The dielectric constants (K at 1 MHz) of these compounds are in the range 14–33 and K shows very little variation in the temperature range 30–100 °C. Their temperature coefficient of dielectric constant (TCK) is negative, which varies from − 21 to − 220 ppm/°C.     

Theoretical investigations on low energy surfaces and nanowires of MgH(2)

The phase stability, chemical bonding, and electronic structure of MgH(2) nanowires and possible low energy surfaces of α-MgH(2) thin films have been investigated using the ab initio projected augmented plane-wave method. Structural optimizations based on total energy calculations predicted that, for the α-MgH(2) phase, the (101) surface is more stable among the possible low energy surfaces. The electronic structure study reveals that the nanowires also have nonmetallic character similar to that of the bulk and thin film phases. Bonding analysis shows that the character of chemical bonding in nanowires has been considerably changed compared with that in bulk phases. Similarly, the bond distances in the surfaces of nanowires are found to be higher than in the bulk material, suggesting that it is possible to remove hydrogen from the nanowires considerably more easily than from bulk crystals.     

1H-NMRD and17O-NMR assessment of water exchange and rotational dynamics of two potential MRI agents: MP-1177 (an extracellular agent) and MP-2269 (a blood pool agent)

The parameters that govern water proton magnetic relaxation (e.g. water exchange rates, and rotational and electronic correlation times) of representatives of two classes of Gd(III) complexes have been estimated, using two different approaches and the results compared with those derived for known analogs. The complexes studied are: (i) the non-ionic GdDTPA-bis(methoxyethyl-amide) [Gd(DTPA-BMEA)], a typical small-molecule extracellular MR agent, and (ii) the ionic Gd(III) complex of 4-pentylbicyclo[2.2.2]octane-1-carboxyl-di-l-aspartyl-lysine-derived-DTPA [GdL]⁴⁻, a prototype MR blood pool agent, which binds to serum albumin in vivo through non-covalent hydrophobic interactions. An¹⁷O-NMR study of [Gd(DTPA-BMEA)] gives a water exchange rate constant ofk _ex ²⁹⁸ =(0.39±0.02)×10⁶ s⁻¹, identical to that for the bismethylamide analog [Gd(DTPA-BMA)]. Both approaches yield longer rotational correlation times for [Gd(DTPA-BMEA)], consistent with its higher molecular weight. An¹⁷O-NMR study of [GdL]⁴⁻ gives a water exchange rate constant ofk _ex ²⁹⁸ =(4.2±0.1)×10⁶ s⁻¹, identical to that for [Gd(DTPA)]²⁻. The water exchange rate on [GdL]⁴⁻ did not decrease considerably when bound to albumin, the lowest limit isk _ex,GdL-BSA=k _ex,GdL/2. Both approaches yield identical rotational correlation times for [GdL]⁴⁻, however, it was difficult to derive a consistent rotational constant for the albumin-bound [GdL]⁴⁻ using the different approaches (values ranged between 1.0 and 23.0 ns).