Kinetics of the Glass Transition of Silica-Filled Styrene–Butadiene Rubber: The Effect of Resins

Resins are important for enhancing both the processability and performance of rubber. Their efficient utilization requires knowledge about their influence on the dynamic glass transition and their miscibility behavior in the specific rubber compound. The resins investigated, poly-(α-methylstyrene) (AMS) and indene-coumarone (IC), differ in molecular rigidity but have a similar aromaticity degree and glass transition temperature. Transmission electron microscopy (TEM) investigations show an accumulation of IC around the silanized silica in styrene–butadiene rubber (SBR) at high contents, while AMS does not show this effect. This higher affinity between IC and the silica surface leads to an increased compactness of the filler network, as determined by dynamic mechanical analysis (DMA). The influence of the resin content on the glass transition of the rubber compounds is evaluated in the sense of the Gordon–Taylor equation and suggests a rigid amorphous fraction for the accumulated IC. Broadband dielectric spectroscopy (BDS) and fast differential scanning calorimetry (FDSC) are applied for the characterization of the dielectric and thermal relaxations as well as for the corresponding vitrification kinetics. The cooling rate dependence of the vitrification process is combined with the thermal and dielectric relaxation time by one single Vogel–Fulcher–Tammann–Hesse equation, showing an increased fragility of the rubber containing AMS

Kinetics of the glass transition of styrene-butadiene-rubber : Dielectric spectroscopy and fast differential scanning calorimetry

The glass transition is relevant for performance definition in rubber products. For extrapolation to high-frequency behavior, time–temperature superposition is usually assumed, although most complex rubber compounds might be outside of its area of validity. Fast differential scanning calorimetry (FDSC) with cooling rates up to 1500 K/s and broadband dielectric spectroscopy (BDS) with frequencies up to 20 MHz are applied here to directly access both kinetics and dynamics of glass formation in a wide frequency range. For the first-time, the relation between the thermal vitrification and the dielectric relaxation is studied on vulcanized styrene-butadiene rubber, showing that both cooling rate and frequency dependence of its glass transition can be described by one single Vogel-Fulcher-Tammann-Hesse equation. The results indicate the validity of the Frenkel-Kobeko-Reiner equation. Another focus is the sample preparation of vulcanized elastomers for FDSC and BDS as well as the temperature calibration below 0°C. © 2020 The Authors. Journal of Applied Polymer Science published by Wiley Periodicals LLC

Anisotropy-induced spin disorder in intergrown, ferrimagnetic Fe7_7 S8_8 polytypes

The monosulfides of the pyrrhotite omission series (Fe$_{1−}$S, 0<≤0.125) are important remanence carriers for paleomagnetic reconstruction of the Earth\u27s crust and extraterrestrial materials. The ferrimagnetic Fe$_7$S$_8$ polytypes are the endmembers, and their stacking modulations of full and vacant layers generate different magnetic anisotropy properties due to the cation-vacancy configurations. In this study, intergrown long-range ordered polytypes with four- and threefold modulation, i.e., 4C and 3C pyrrhotite, were prepared in a diffusion-driven process by quenching of a natural pyrrhotite crystal with randomized vacancies. In addition, a third constituent with coherence lengths of a few nanometers, denoted 3C*, was found that exhibits spin-glass behavior at about 10 K due to local magnetic anisotropies arising from vacancy-density variations. The concomitant occurrence of this nano-scale constituent with spin disorder and the long-range ordered polytypes indicate competitive diffusion-driven processes during Fe$_7$S$_8$ formation. Such information provides insight into the provenance and genesis of ferrimagnetic pyrrhotite in Earth and extraterrestrial systems and in a broader sense into vacancy-induced materials

Competition between Structural Relaxation and Crystallization in the Glass Transition Range of Random Copolymers

Structural relaxation in polymers occurs at temperatures in the glass transition range and below. At these temperatures, crystallization is controlled by diffusion and nucleation. A sequential occurrence of structural relaxation, nucleation, and crystallization was observed for several homopolymers during annealing in the range of the glass transition. It is known from the literature that all of these processes are strongly influenced by geometrical confinements. The focus of our work is copolymers, in which the confinements are caused by the random sequence of monomer units in the polymer chain. We characterize the influence of these confinements on structure formation and relaxation in the vicinity of the glass transition. The measurements were performed with a hydrogenated nitrile-butadiene copolymer (HNBR). The kinetics of the structural relaxation and the crystallization was measured using fast differential scanning calorimetry (FDSC). This technique was selected because of the high sensitivity, the fast cooling rates, and the high time resolution. Crystallization in HNBR causes a segregation of non-crystallizable segments in the macromolecule. This yields a reduction in mobility in the vicinity of the formed crystals and as a consequence an increased amount of so-called &ldquo;rigid amorphous fraction&rdquo; (RAF). The RAF can be interpreted as self-assembled confinements, which limit and control the crystallization. An analysis of the crystallization and the relaxation shows that the kinetic of both is identical. This means that the Kohlrausch exponent of relaxation and the Avrami exponent of crystallization are identical. Therefore, the crystallization is not controlled by nucleation but by diffusion and is terminated by the formation of RAF

Kinetics of the Glass Transition of Silica-Filled Styrene&ndash;Butadiene Rubber: The Effect of Resins

Resins are important for enhancing both the processability and performance of rubber. Their efficient utilization requires knowledge about their influence on the dynamic glass transition and their miscibility behavior in the specific rubber compound. The resins investigated, poly-(&alpha;-methylstyrene) (AMS) and indene-coumarone (IC), differ in molecular rigidity but have a similar aromaticity degree and glass transition temperature. Transmission electron microscopy (TEM) investigations show an accumulation of IC around the silanized silica in styrene&ndash;butadiene rubber (SBR) at high contents, while AMS does not show this effect. This higher affinity between IC and the silica surface leads to an increased compactness of the filler network, as determined by dynamic mechanical analysis (DMA). The influence of the resin content on the glass transition of the rubber compounds is evaluated in the sense of the Gordon&ndash;Taylor equation and suggests a rigid amorphous fraction for the accumulated IC. Broadband dielectric spectroscopy (BDS) and fast differential scanning calorimetry (FDSC) are applied for the characterization of the dielectric and thermal relaxations as well as for the corresponding vitrification kinetics. The cooling rate dependence of the vitrification process is combined with the thermal and dielectric relaxation time by one single Vogel&ndash;Fulcher&ndash;Tammann&ndash;Hesse equation, showing an increased fragility of the rubber containing AMS

TOPEM® – the new advanced multifrequency temperature modulated DSC technique

TOPEM® is a new temperature modulated DSC technique based on a stochastic temperature modulation superimposed to a conventional underlying DSC temperature program. Analysis of the temperature input and the heat flow output signal delivers the quasi static heat capacity as well as the quasi static reversing and non reversing heat flows. Furthermore, also the frequency dependent complex heat capacity of the sample can be computed in a wide frequency range. All this information is available from one single TOPEM® measurement

Stochastic temperature modulation : a new technique in temperature-modulated DSC

A new temperature-modulated differential scanning calorimetry (TMDSC) technique is introduced. The technique is based on stochastic temperature modulation and has been developed as a consequence of a generalized theory of a temperature-modulated DSC. The quasi-static heat capacity and the frequency-dependent complex heat capacity can be determined over a wide frequency range in one single measurement without further calibration. Furthermore, the reversing and non-reversing heat flows are determined directly from the measured data. Examples show the frequency dependence of the glass transition, the isothermal curing of thermosets and a solid–solid transition