Magnetic polymer composites containing recycled neodymium-iron-boron (NdFeB) powder and natural rubber (NR) were prepared by the two-roll mill technique. Their mechanical and cure properties were studied as a function of NdFeB loading from 0-120 phr. With increasing magnetic loading, the cure time of the NdFeB-NR composites were exponentially decreased because of the reduction of the polymer chain crosslink. The tensile strength of the NR compound, related to the cure characteristics, was reduced by 40% by the addition of 10 phr NdFeB fillers because of the inhibition of the stress-induced crystallization. However, the variation in loading from 30-90 phr has modest effects on the tensile strength as well as elongation at break and the hardness. Furthermore, recycled NdFeB-NR composites had higher modulus and lower percentage of swelling in this magnetic loading regime. Simple tests confirmed the distribution of magnetic stray field around pieces of NdFeB-NR composites.
Epoxidized low molecular weight natural rubber (ELMWNR) with 28 mol% epoxide groups and weight average molecular weight of 49,000 g mol À1 was prepared by oxidative degradation of epoxidized natural rubber (NR) using periodic acid in the latex state. ELMWNR-28 was used at 10 parts per hundred parts of rubber (phr) loading in combination with bis-(triethoxysilylpropyl) tetrasulfide (TESPT) as the silane coupling agent in the range of 0-4.5 phr in silica-reinforced NR compounds. The use of TESPT in combination with ELMWNR-28 gives lower mixing torques and compound viscosities compared with the use of TESPT alone and the system without any compatibilizer. The bound rubber content, modulus, and tensile strength of the compounds with only TESPT strongly depend on the TESPT loading. The use of ELMWNR-28 as a compatibilizer clearly improves such properties compared with the non-compatibilized systems. By adding TESPT into the compound with ELMWNR-28, the properties further improve with increasing TESPT loading. The combined effect of ELMWNR-28 at 10 phr with a small amount of TESPT at 1.5 phr results in compounds with superior processability (i.e. low Mooney viscosity and Payne effect), and only slightly lower modulus and Downloaded from reinforcement index (M300/M100) compared with the use of the optimum content of TESPT. This compatibilizer/TESPT combination has the environmental benefits that the ELMWNR is a naturally based product, and that the reduced amount of TESPT silane coupling agent emits a greatly reduced amount of ethanol during processing.
This work investigates the effect of epoxidized low molecular weight natural rubber (ELMWNR) in silica- and carbon black-filled natural rubber (NR) compounds on processing and mechanical and dynamic mechanical properties. The ELMWNRs with different mol% epoxide content were prepared from depolymerization of epoxidized NR using periodic acid in latex state to have a molecular weight in a range of 50 000–60 000 g/mol. Their chemical structures and actual mol% of epoxide were analyzed by 1H NMR. The ELMWNRs were added to the filled NR compounds as compatibilizers at varying loadings from 0 to 15 phr. The addition of ELMWNR decreases compound viscosity and the Payne effect, that is, filler–filler interaction, of the silica-filled compound. In the silica–silane compound and the compound with 28 mol% epoxide (ELMWNR-28), the compound viscosities are comparable. The optimal mechanical properties of silica-filled vulcanizates are obtained at the ELMWNR-28 loading of 10 phr. In contrast, the addition of ELMWNR to a carbon black-filled compound shows only a plasticizing effect. The incorporation of ELMWNR into NR compounds introduces a second glass transition temperature and affects their dynamic mechanical properties. Higher epoxide contents lead to higher loss tangent values of the rubber vulcanizates in the range of the normal service temperature of a tire.
Physical properties of polyurethane (PU) can be modified for desired applications by adding appropriate fillers. In this work, cobalt (Co) powder of average diameter 2 μπι was filled in PU elastomers synthesized by a reaction between polyol and diisocyanate. Variation of Co loading (0, 20,40 and 60 wt.%) modified thermal properties of PU composites in terms of the shift in a melting temperature and the increase in heat absorption. From DC hysteresis loops, PU/Co composites exhibited ferromagnetic properties with improved magnetizations by the increase in Co loading. On the other hand, the coercive field was almost unvaried. For high frequency electromagnetic behaviors, the complex electrical permittivity (ε-je") and magnetic permeability (μ'-]μ") were sensitive to the frequency from 10 MHz up to 100 MHz and reached the modest values in the regime between 100 MHz and 1 GHz. At each frequency, the real part of permeability and permittivity of PU were raised by the inclusion of Co fillers. While the thermal behaviors were explained using the interaction between Co clusters and the PU matrix, the electromagnetic properties can be understood by taking into the account of interactions between Co clusters at high loading levels.
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