scholarly journals Dielectric Relaxation Spectroscopy in Synthetic Rubber Polymers: Nitrile Butadiene Rubber and Ethylene Propylene Diene Monomer

2020 ◽  
Vol 2020 ◽  
pp. 1-15
Author(s):  
Young Il Moon ◽  
Jae Kap Jung ◽  
Ki Soo Chung

The dielectric permittivity of synthetic rubber polymers, nitrile butadiene rubber (NBR) and ethylene propylene diene monomer (EPDM), with both frequency and temperature variations, was thoroughly investigated by dielectric relaxation spectroscopy (DRS). The spectrum versus frequency of DRS was analyzed with the semiempirical Havriliak–Negami formula and conductivity contribution by employing the newly developed “dispersion analyzer” analysis program. The main dielectric relaxations called the α- and β-processes, associated with the cooperative motion of chains in polymers, were discovered in the low-temperature region. In the high-temperature region, we found Maxwell–Wagner–Sillars (MWS) relaxation associated with polymer interfacing and normal-mode (α’) relaxation responsible for end-to-end dipole vector motion. The activation energies of schematic molecular chains responsible for the relaxation processes were obtained with the information about its motional mode. The glass transition temperature and dipole moment for the side group were also determined and compared with those from previous studies. In the EPDM specimen, the peaks of α- and β-relaxation merged at high temperature and were separated with decreasing temperature. The first observations of both merging and splitting were consistent with the results on the temperature dependency of the relaxation strength. Both contour mapping and three-dimensional plots for the two rubbers provide visual information for the distribution and mapping of relaxation.

2020 ◽  
Vol 2020 ◽  
pp. 1-15
Author(s):  
Jae Kap Jung ◽  
Young Il Moon ◽  
Gyung Hyun Kim ◽  
Nae Hyung Tak

We invented a dispersion analysis program that analyzes the relaxation processes from dielectric permittivity based on a combination of the Havriliak–Negami and conductivity contribution functions. By applying the created program to polymers such as nitrile butadiene rubber (NBR) and ethylene propylene diene monomer (EPDM), several relaxation processes were characterized: an α process due to segmental motions of the C-C bond, an α′ process attributed to fluctuations in the end-to-end dipole vector of the polymer chain, the conduction contribution by the filler observed above room temperature, and secondary relaxation processes β and γ of motion for the side group in NBR. In the EPDM specimen, the β process associated with the rotational motion of the side groups, the α process associated with the relaxation of local segmental motion, and the αβ process associated with the origin of the β process at high temperatures above 305 K were observed. The Maxwell–Wagner–Sillars effect and conduction contribution were also presented. The molecular chains responsible for the relaxation processes were assigned by building molecular models of the two polymers. The temperature dependence of the relaxation strength and the shape parameters that characterize the process were investigated. From the temperature-dependent relaxation analysis, the merged αβ process, activation energy, and glass transition temperature were determined and compared.


e-Polymers ◽  
2020 ◽  
Vol 20 (1) ◽  
pp. 482-490
Author(s):  
Meng Song ◽  
Xiulin Yue ◽  
Xiujuan Wang ◽  
Mengjie Huang ◽  
Mingxing Ma ◽  
...  

AbstractBy introducing hindered amine GW-622 or GW-944 into nitrile-butadiene rubber/phenolic resin (NBR/PR, abbreviated as NBPR) matrix, we have prepared different hindered amine/NBR/PR ternary hybrid damping materials with high-temperature damping performance, respectively. Fourier transform infrared (FTIR) spectroscopy, scanning electron microscope (SEM), differential scanning calorimetry (DSC), and dynamic thermomechanical analysis (DMA) were used to research the microstructure, compatibility, and damping properties of the hindered amine/NBPR composites. FTIR results indicate that hydrogen bonds are formed between the hindered amine and the NBPR matrix. Both DSC and SEM results show that hindered amine has partial compatibility with the NBPR matrix. DMA results show that two loss peaks appear in the hindered amine/NBPR composite. Thereby, the composites show better damping performance at a higher temperature, and the temperature domain of high-temperature damping becomes wider with the increase in the addition of hindered amine. This study provides a theoretical support for the preparation of high-temperature damping materials.


2017 ◽  
Vol 44 (5) ◽  
pp. 25-28 ◽  
Author(s):  
A.A. Zuev ◽  
L.R. Lyusova ◽  
N.P. Boreiko

Now there is not a single area of industry that can do without adhesive elastomer materials. Composites based on synthetic rubbers comprise 75% of the total volume of adhesive materials produced, which is due to the combination of unique properties typical of the elastomer base of the adhesive. The base of many imported adhesives for the bonding of rubber to metal is chlorinated natural rubber. As an alternative, chlorinated synthetic isoprene rubber has been proposed, developed at the Scientific Research Institute for Synthetic Rubber in St Petersburg. The chlorinated isoprene rubber was compared with imported chlorinated natural rubber in adhesive composites, and the physicomechanical properties of mixes based on a blend of chlorinated rubber and nitrile butadiene rubber were investigated. The investigation was conducted on chlorinated natural rubber of grade Pergut S20, chlorinated isoprene rubber SKI-3, and nitrile butadiene rubbers of grades BNKS-28AMN and SKN-26S. The influence of the ratio of chlorinated rubber to nitrile butadiene rubber and the technological factors of mix preparation on the properties of films produced from them was established. It was shown that, in terms of the level of properties, home-produced chlorinated rubber can be used as the base for adhesives for hot bonding of rubber to metal instead of imported Pergut S20.


2016 ◽  
Vol 49 (4) ◽  
pp. 298-314 ◽  
Author(s):  
Sara Estagy ◽  
Saeed Ostad Movahed ◽  
Soheil Yazdanbakhsh ◽  
Majid Karim Nezhad

The market for commercial polymer blends has grown steadily. A good blend should have strong interphases between different parts of the constituted polymers. Lack of strong interphases is a classical problem of the blend industry. Ethylene-propylene-diene monomer rubber (EPDM)/styrene-butadiene rubber (SBR) blends have a very good aging resistance and good compression sets. However, these rubbers are partially miscible. To improve the miscibility of EPDM and SBR in their blends, a Lewis acid, AlCl3, was used to form EPDM–g–SBR copolymer through Friedel–Crafts reactions. The existence of covalent bonds between EPDM and SBR macromolecules was studied by the cure traces of the blends, that is, ΔTorque, Fourier transform infrared spectrums, differential scanning calorimetry (DSC) heat flow curves, thermogravimetric analysis curves, and scanning electron (SEM) micrographs. Subsequently, several blends with EPDM/SBR ratio of 40/60 and with various AlCl3 amounts were prepared and after curing, their mechanical properties were measured and compared. The results showed covalent bonds formed between SBR–EPDM and SBR–SBR macromolecules. An exothermic change in heat flow in the DSC curve was observed around 111.28°C, which can be attributed to the formation of carbocations in Friedel–Crafts reactions. Adding 2 phr AlCl3 had an efficient effect on EPDM–SBR and or SBR–SBR linkages. The mechanical properties of the cured blends, that is, tensile strength were lower when compared with corresponding values for prepared compound with SBR. Excellent compatibility between the two polymers and strong interphases were observed in SEM micrograph of the cured blend with 1 phr AlCl3.


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