Modeling carbon black reinforcement in rubber compounds

One of the advocated reinforcement mechanisms is the formation by the filler of a network interpenetrating the polymer network. The deformation and reformation of the filler network allows the explanation of low strain dynamic physical properties of the composite. The present model relies on a statistical study of a collection of elementary mechanical systems, This leads to a mathematical approach of the complex modulus G* = G' + iG". The storage and loss modulus (G' and G", respectively), are expressed in the form of two integrals capable of modeling their Variation with respect to strain

Storage of solid propellants in a dry environment

Storage of solid propellants in either a dry or a vacuum environment causes a significantly greater increase in the propellants' modulus and maximum tensile strength than does ambient storage. It is postulated that these physical property changes can be attributed to the effect trace amount of moisture has on the bond between the propellants' binder and oxidizer

An ultra melt-resistant hydrogel from food grade carbohydrates

© 2017 The Royal Society of Chemistry. We report a binary hydrogel system made from two food grade biopolymers, agar and methylcellulose (agar-MC), which does not require addition of salt for gelation to occur and has very unusual rheological and thermal properties. It is found that the storage modulus of the agar-MC hydrogel far exceeds those of hydrogels from the individual components. In addition, the agar-MC hydrogel has enhanced mechanical properties over the temperature range 25-85 °C and a maximum storage modulus at 55 °C when the concentration of methylcellulose was 0.75% w/v or higher. This is explained by a sol-gel phase transition of the methylcellulose upon heating as supported by differential scanning calorimetry (DSC) measurements. Above the melting point of agar, the storage modulus of agar-MC hydrogel decreases but is still an elastic hydrogel with mechanical properties dominated by the MC gelation. By varying the mixing ratio of the two polymers, agar and MC, it was possible to engineer a food grade hydrogel of controlled mechanical properties and thermal response. SEM imaging of flash-frozen and freeze-dried samples revealed that the agar-MC hydrogel contains two different types of heterogeneous regions of distinct microstructures. The latter was also tested for its stability towards heat treatment which showed that upon heating to temperatures above 120 °C its structure was retained without melting. The produced highly thermally stable hydrogel shows melt resistance which may find application in high temperature food processing and materials templating

Oxidation induced changes in viscoelastic properties of a thermostable epoxy matrix

The thermal ageing of a neat epoxy matrix has been studied at 200°C in air by three complementary analytical techniques: optical microscopy, mechanical spectrometry and nano-indentation. Thermal oxidation is restricted in a superficial layer of about 195 µm of maximal thickness. It consists in a predominant chain scission process involving, in particular, chemical groups whose β motions have the highest degree of cooperativity and thus, are responsible for the high temperature side of β dissipation band. As a result, chain scissions decrease catastrophically the glass transition temperature, but also increase significantly the storage modulus at glassy plateau between Tβ and Tα. This phenomenon is called “internal antiplasticization”. Starting from these observations, the Di Marzio and Gilbert’s theories have been used in order to establish relationships between the glass transition temperature and number of chain scissions, and between the storage modulus and β transition activity respectively. The challenge is now to establish a relationship between the transition activity and the concentration of the corresponding chemical group

Anelastic relaxor behavior of Pb(Mg1/3Nb2/3)O3

Elastic storage modulus and loss of relaxor lead magnesium niobate ceramics, Pb(Mg1/3Nb2/3)O3, have been measured with dynamic mechanical analyzer in single cantilever mode in the temperature range from 170 K to 320 K and at frequencies from 0.1 Hz to 50 Hz. The dependence of the elastic susceptibility (inverse modulus) on temperature and frequency of the driving force has characteristics of typical relaxor behavior that can be well described with the Vogel-Fulcher law. The parameters of the Vogel-Fulcher relation exhibit similar values for the dielectric and anelastic relaxations. Similarities and differences between anelastic and dielectric relaxor behaviors are identified.Comment: accepted in Applied Physics Letter

Structural build-up of cementitious paste with nano-Fe3O4 under time-varying magnetic fields

The structural build-up of cementitious paste with nano-Fe3O4 under time-varying magnetic fields was experimentally investigated using small amplitude oscillatory shear (SAOS) technique. Several modes of magnetic fields, such as constant, sudden-changed and linearly-changed, were applied to the cementitious paste. Results showed that the structural build-up of the cementitious paste depended on the magnetizing time and magnetic field strength. Applying constant magnetic fields improved the liquid-like behavior during first minutes and afterwards the solid-like property was enhanced. Both the sudden-increased and sudden-decreased magnetic fields resulted in a sharp decrease in storage modulus. The linearly increasing magnetic field resulted in a slight increase in storage modulus but higher liquid-like behavior. When the magnetic field was linearly decreased from 0.5 T to approx. 0.25 T, the structural build-up was enhanced significantly, and with the continuously decreasing magnetic field from approx. 0.25 T to 0 T, a decrease in storage modulus was observed

Dynamics of a colloidal glass during stress-mediated structural arrest

We employ parallel superposition rheology to study the dynamics of an aging colloidal glass in the presence of a mean field stress. Over a range of intermediate stresses, the loss modulus exceeds the storage modulus at short times but develops a maximum concomitant with a crossover between the two as the system ages. This is attended by a narrowing of the loss peak on increasing stress. We show that this feature is characteristic of the structural arrest in these materials, which is made observable on reasonable timescales by the activating influence of the stress. The arrest time displays an exponential dependence on inverse stress. These results provide experimental validation of the role of stress as an effective temperature in soft glassy systems as has been advanced in recent theoretical frameworks.Comment: 5 pages, 5 figure