Effects of different kind of sesame materials on the physical properties of gomatofu (sesame tofu)

Gomatofu (sesame tofu) is one of the traditional Japanese healthy foods and is representative of all shojin (vegetarian) dishes. Gomatofu, one of the mixed gels consisting of kudzu (arrowroot) starch and sesame, possesses an extremely unusual textural characteristic which is soft, smooth, and springy. The textural properties are greatly influenced by preparation, ingredients and roasting conditions of sesame seeds. Hence there are many kinds of sesame materials which can be used to prepare gomatofu such as white, black, huskless or not and roasted or unroasted sesame materials, in this study, the effects of these materials on the physical properties of gomatofu were studied. The sample of Ra-W prepared with unroasted huskless sesame seed had the least hardness, but mouthfeel of this sample were the highest. The samples of Ro-B and Ro-W prepared with roasted husk (black and white) sesame seed were evaluated to have the best palatability because of their superior springiness. It was clarified that different kinds of sesame materials affected the forming of structure and physical properties of gomatofu, because the chemical components were different from varieties of sesame materials.     

Viscoelastic State for the Solutions of Spherically Symmetric Viscoelasticity Problems

The solutions of the spherically symmetric, linear, isothermal, and transient viscoelasticity problems via reciprocity theorem have been investigated for a specific material. The integral form of stress–strain relations has been used. The Laplace transform of a viscoelastic state, which is necessary for the integral equation arising as a result of reciprocity theorem, has been derived. This integral equation has been solved by Laplace transform. A sample problem has been solved to test the presented formulation. A numerical application of the analytic solution of this problem has been given.     

Random Vibration of Systems with Viscoelastic Memory

The equation of motion of linear dynamic systems with viscoelastic memory is usually expressed in a integrodifferential form, and its numerical solution is computationally heavy. In two recent papers, the writers suggested that the system memory be accounted for through the introduction of a number of additional internal variables. Following this approach, the motion of the system is governed by a set of first-order, linear differential equations, whose solution is quite easy. In this paper, the approach is extended to single-degree-of-freedom systems subjected to random, nonstationary excitation. The equations governing the time variation of the second-order statistics are derived, and an effective step-by-step solution procedure is proposed. Numerical example shows the accuracy of the procedure for white and nonwhite excitations.     

Estimation of rheological parameters using velocity measurements

In the present investigation, we develop a method for estimating rheological parameters of viscoelastic fluids using velocity measurement in a square straight channel. It is believed that a somewhat complicated patterns of secondary flows due to the non-zero second normal stress difference are more useful than the simple viscometric flows traditionally adopted in the determination of rheological parameters. The inverse problem of determining the rheological parameters from a set of velocity measurements is solved using a conjugate gradient method. When applied to a general constitutive equation encompassing the UCM model, the Oldroyd-B model and the PTT model, the present method is found to yield a reasonably accurate estimation of five rheological parameters simultaneously even with noisy velocity measurements.     

Phase morphology and melt viscoelastic properties in blends of ethylene/vinyl acetate copolymer and metallocene-catalysed linear polyethylene

The aim of this study was to determine the linear viscoelastic properties of a series of ethylene/vinyl acetate copolymer/metallocene-catalysed polyethylene (mPEs) blends. Newtonian viscosity showed a pronounced positive deviation from the double reptation model, which assumes miscibility or, at least, cooperative relaxation between the mixed species. Enhanced values of steady-state compliance and elastic indices with respect to those of the pure components were also noted. These features are typical of emulsion-like polymer blends and are thought to arise from additional relaxation processes associated with dispersed phase deformability. Application of the Palierne model for emulsions of two viscoelastic liquids showed good agreement with our experimental dynamic results at both ends of the phase diagram. However, the model failed at intermediate compositions. Through the application of several rheological criteria we were able to locate the phase inversion concentration at a weight fraction of w=0.60 in the mPEs. It is suspected that, in this composition range, a fully co-continuous phase develops due to the phase inversion mechanism, which has considerable effects on the viscoelastic properties of the blends.     

Large macro-dipoles generated in a supramolecular polymer of N,N′,N″-tris(3,7-dimethyloctyl)benzene-1,3,5-tricarboxamide in n-decane

A supramolecular polymer formed by N,N′,N″-tris(3,7-dimethyloctyl)benzene-1,3,5-tricarboxamide (DO₃B) in n-decane (C₁₀) possesses large macro-dipoles naturally generated by three-fold inter-molecular hydrogen bonding aligned along its helical columnar structure connected by defective portions, which are DO₃B molecules containing failure in the hydrogen bond formation, in the order of head to tail arrangement without dipole inversion like type-A polymers.     

Factors influencing encapsulation behavior in composite droplet-type polymer blends

In this study the influence of the molecular weight of the dispersed phase components on encapsulation effects in the composite droplet phase was examined for high density polyethylene (HDPE)/PS/PMMA ternary blends. Three different blends composed of various PS and PMMA materials dispersed in an HDPE matrix were prepared using an internal mixer. The morphology was studied by light and electron microscopy. Current models used for predicting encapsulation effects and composite droplet formation in ternary systems (based on static interfacial tension) predict in all cases that PS will encapsulate the PMMA. However, in one case, an unexpected encapsulation of PS by PMMA was observed. It was found that arguments based on the effect of viscosity ratio or the absolute viscosity of the different dispersed phases do not explain that discrepancy. In addition, the reversal of that latter composite droplet morphology from PMMA encapsulating PS to PS encapsulating PMMA was observed upon annealing treatment. Considering all the above, a conceptual model was developed to predict encapsulation effects in composite droplet type systems based on the use of a dynamic interfacial tension (i.e. taking into account the elasticity of the polymer components). Calculations based on the dynamic interfacial tension model, using elasticities based on constant shear stress, were able to account for all of the observed encapsulation effects in this study.     

Light scattering and viscoelasticity study of poly(vinyl alcohol)-borax aqueous solutions and gels

Poly(vinyl alcohol)-borate (PVA-borate) aqueous solutions properties with PVA concentrations ranging from 2 to 60 g/L and borax concentrations of 0.0 and 0.2 M were investigated at room temperature using static and dynamic light scattering (SLS and DLS), and dynamic viscoelasticity measurements. Light scattering and viscoelasticity data revealed that all the PVA-borate aqueous systems, except those with [PVA]≥40 g/L and [borax]=0.2 M, behaved as solutions. For PVA-borate aqueous systems with [PVA]≥40 g/L and [borax]=0.2 M, light scattering data revealed that these systems behaved like gels, but viscoelasticity data showed that these systems were in flow states. The experimental data suggest that PVA-borate aqueous systems with [PVA]≥40 g/L and [borax]=0.2 M are thermoreversible gels with finite equilibrium life time of thermoreversible borate-PVA di-diol crosslinks. The thermoreversible crosslinks can be observed by the non-perturbing light scattering technique but not by the pertubing rheometric method. These results indicate the advantage of light scattering relative to rheometers for studying the physical or reversible crosslink gels.     

The viscoplastic properties of crude oil-water interfaces

The breaking of water-in-crude oil emulsions is a major challenge in the conventional petroleum industry, while oil-in-water emulsions present similar issues in commercial oilsands extraction processes. The stability of these emulsions can be attributed to complex rheological properties of the crude oil-water interface. Novel micromechanical techniques are developed that allow direct measurements of interfacial behaviour of emulsion drops. In these techniques, individual emulsion drops are elongated using micropipettes, where one micropipette is shaped into a cantilever for force measurements. As such, the surface behaviour of a drop is recorded in stress-strain experiments. In an alternative technique, the extended drop is released from a micropipette, and its natural, tension-driven relaxation is observed.The surface behaviour of bitumen (a heavy crude oil) emulsion drops in aqueous environments, that include dissolved calcium ions and suspended montmorillonite clays, is studied. The plasticity and other surface properties of these bitumen drops are discussed. A simple, lumped-parameter model is developed to describe the recovery of a bitumen drops to their final non-spherical shapes.     

Viscoelastic effects on the scratch resistance of polymers: relationship between mechanical properties and scratch properties at various temperatures

Scratch durability of polymer surfaces and coatings is becoming critical for the increasing use of these materials in new applications, replacing other materials with harder surfaces.

Scratch resistance of polymers has been the subject of numerous studies, which have led to specific definitions for plastic deformation characterization and fracture resistance during scratch testing. Viscoelastic and viscoplastic behavior during a scratch process have been related to dynamic mechanical properties that can be measured via dynamic nano-indentation testing. Yet, the understanding of the origin of the fracture process of a polymer during scratch remains approximate. Parameters like tip shape and size, scratch velocity and loading rate, applied strain and strain rates, have been considered critical parameters for the fracture process, but no correlation has been clearly established.

The goal of this work is to define and analyze scratch parameters that relate to mechanical properties. The evolution of scratch resistance parameters as a function of temperature and strain rate, compared to the evolution of dynamic mechanical properties obtained from indentation and uniaxial tensile tests over a range of temperature for poly(methyl methacrylate) (PMMA) helped in identifying a correlation between the tensile stress–strain behavior and scratch fracture toughness.

This correlation brings a new understanding of the origin of the fracture mechanisms during a scratch process. In particular, it is demonstrated that the characteristic strain applied by the indenter is a most relevant parameter to describe the fracture resistance during a scratch process, independently of the indenter geometry.