Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Viscoelastic evaluations

Ito, H., Kumari, R., Takatani, M., Okamoto, T., Hattori, H., and Fujiyoshi, I., Viscoelastic Evaluation of Effects of Fiber Size and Composition on Cellulose-Polypropylene Composite of High Filler Content, Polym. Eng. Set, 48, 415 (2008)... [Pg.55]

Adeyeye MC, Jain AC, Ghorab MK, Reilly WJ Jr. Viscoelastic evaluation of topical creams containing microcrystalline cellulose/ sodium carboxymethylcellulose as stabilizer. AAPS PharmSciTech 2002 3(2) E8. [Pg.123]

Ishii, D., Saito, T., Isogai, A. Viscoelastic Evaluation of Average Length of Cellulose Nanofibers Prepared by TEMPO-Mediated Oxidation. Biomactomolecules. 12, 548-550 (2011)... [Pg.110]

The paper discusses the application of dynamic indentation method and apparatus for the evaluation of viscoelastic properties of polymeric materials. The three-element model of viscoelastic material has been used to calculate the rigidity and the viscosity. Using a measurements of the indentation as a function of a current velocity change on impact with the material under test, the contact force and the displacement diagrams as a function of time are plotted. Experimental results of the testing of polyvinyl chloride cable coating by dynamic indentation method and data of the static tensile test are presented. [Pg.239]

In principle, the relaxation spectrum H(r) describes the distribution of relaxation times which characterizes a sample. If such a distribution function can be determined from one type of deformation experiment, it can be used to evaluate the modulus or compliance in experiments involving other modes of deformation. In this sense it embodies the key features of the viscoelastic response of a spectrum. Methods for finding a function H(r) which is compatible with experimental results are discussed in Ferry s Viscoelastic Properties of Polymers. In Sec. 3.12 we shall see how a molecular model for viscoelasticity can be used as a source of information concerning the relaxation spectrum. [Pg.167]

The transition to turbulent flow begins at Re R in the range of 2,000 to 2,500 (Metzuer and Reed, AIChE J., 1, 434 [1955]). For Bingham plastic materials, K and n must be evaluated for the condition in question in order to determine Re R and establish whether the flow is laminar. An alternative method for Bingham plastics is by Hanks (Hanks, AIChE J., 9, 306 [1963] 14, 691 [1968] Hanks and Pratt, Soc. Petrol. Engrs. J., 7, 342 [1967] and Govier and Aziz, pp. 213-215). The transition from laminar to turbulent flow is influenced by viscoelastic properties (Metzuer and Park, J. Fluid Mech., 20, 291 [1964]) with the critical value of Re R increased to beyond 10,000 for some materials. [Pg.640]

Grace [18] evaluated t% as a function of 8 for viscoelastic matrices. His results are shown in Fig. 10. The reduced time increases as the viscosity ratio increases. If the residence time during a processing is less than... [Pg.691]

Then, for a particulate composite, consisting of a polymeric matrix and an elastic filler, it is possible by the previously described method to evaluate the mechanical and thermal properties, as well as the volume fraction of the mesophase. The mesophase is also expected to exhibit a viscoelastic behaviour. The composite consists, therefore, of three phases, out of which one is elastic and two viscoelastic. [Pg.155]

This second group of tests is designed to measure the mechanical response of a substance to applied vibrational loads or strains. Both temperature and frequency can be varied, and thus contribute to the information that these tests can provide. There are a number of such tests, of which the major ones are probably the torsion pendulum and dynamic mechanical thermal analysis (DMTA). The underlying principles of these dynamic tests have been covered earlier. Such tests are used as relatively rapid methods of characterisation and evaluation of viscoelastic polymers, including the measurement of T, the study of the curing characteristics of thermosets, and the study of polymer blends and their compatibility. They can be used in essentially non-destructive modes and, unlike the majority of measurements made in non-dynamic tests, they yield data on continuous properties of polymeric materials, rather than discontinuous ones, as are any of the types of strength which are measured routinely. [Pg.116]

The consequences of the wetting ridge in the capillary penetration of a liquid into a small-diameter tube have been evaluated. Viscoelastic braking reduces the liquid flow rate when viscoelastic dissipation outweighs the viscous drag resulting from Poiseuille flow. [Pg.312]

Viscoelastic properties have been discussed in relation to molar mass, concentration, solvent quality and shear rate. Considering the molecular models presented here, it is possible to describe the flow characteristics of dilute and semi-dilute solutions, as well as in simple shear flow, independent of the molar mass, concentration and thermodynamic quality of the solvent. The derivations can be extended to finite shear, i.e. it is possible to evaluate T) as a function of the shear rate. Furthermore it is now possible to approximate the critical conditions (critical shear rate, critical rate of elongation) at which the onset of mechanical degradation occurs. With these findings it is therefore possible to tune the flow features of a polymeric solution so that it exhibits the desired behaviour under the respective deposit conditions. [Pg.40]

Figure 4 shows stress-strain curves measured at an extension rate of 94% per minute on the TIPA elastomer at 30°, —30°, and —40°C. With a decrease in temperature from 30° to -40°C, the ultimate elongation increases from 170% to 600%. The modulus Ecr(l), evaluated from a one-minute stress-strain isochrone, obtained from plots like shown in Figure 1, increases from 1.29 MPa at 30°C to only 1.95 MPa at —40°C. This small increase in the modulus and the large increase in the engineering stress and elongation at fracture results from viscoelastic processes. [Pg.431]

After several cycles of the compression and expansion, the dynamic jc-A curve becomes a single closed loop, somewhat distorted from a genuine ellipsoid. In order to analyze the forms of the hysteresis loop under stationary conditions, we have measured the time trace of the dynamic surface pressure after five cycles of the compression and expansion, and then Fourier-transformed it to the frequency domain. The Fourier-transformation was adapted to evaluate the nonlinear viscoelasticity in a quantitative manner. The detailed theoretical consideration for the use of the Fourier transformation to evaluate the nonlinearity, are contained in the published articles [8,43]. [Pg.245]

The inverse problem is to evaluate the viscoelasticity pattern from the experimental (or simulated) strain data. [Pg.222]

Rossi et al. [30] evaluated rheologically mucins of different origin with polyacrylic acid and sodium carboxymethyl cellulose. The same group also reported a novel rheological approach based on a stationary viscoelastic test (creep test) to describe the interaction between mucoadhesive polymers and mucins [31,32]. Jabbari et al. [33] used attenuated total-reflection infrared spectroscopy to investigate the ehain interpenetration of polyaciylic acid in the mucin interface. [Pg.177]

Note 5 Creep is sometimes described in terms of non-linear viscoelastic behaviour, leading, for example, to evaluation of recoverable shear and steady-state recoverable shear compliance. The definitions of such terms are outside the scope of this document. [Pg.166]


See other pages where Viscoelastic evaluations is mentioned: [Pg.502]    [Pg.502]    [Pg.80]    [Pg.90]    [Pg.93]    [Pg.150]    [Pg.150]    [Pg.155]    [Pg.162]    [Pg.192]    [Pg.199]    [Pg.128]    [Pg.44]    [Pg.72]    [Pg.84]    [Pg.282]    [Pg.107]    [Pg.115]    [Pg.554]    [Pg.616]    [Pg.32]    [Pg.424]    [Pg.430]    [Pg.601]    [Pg.190]    [Pg.3]    [Pg.17]    [Pg.237]    [Pg.224]    [Pg.117]    [Pg.222]    [Pg.8]   


SEARCH



© 2024 chempedia.info