Dependence of the Ultimate Properties of a SBR Rubber on Strain Rate and Temperature

1959 ◽  
Vol 32 (4) ◽  
pp. 992-1004 ◽  
Author(s):  
Thor L. Smith

Abstract The tensile strength and ultimate elongation of polymeric materials depend on both the temperature and experimental time scale. The mechanical properties of amorphous polymers at temperatures above their glass transition temperature Tg are more amenable to treatment in terms of molecular theories than are their mechanical properties at temperatures below Tg or the mechanical properties of crystalline polymers. For amorphous polymers at temperatures above Tg the viscoelastic properties in small deformations have been studied rather extensively, and several molecular theories—essentially identical—have been published. In contrast, few systematic studies have been made of the effect of time and temperature on the ultimate properties. Consequently, only a limited amount of data is available which can serve as a basis for developing and verifying molecular theories dealing with ultimate properties. A recent theory by F. Bueche treats the time and temperature dependence of tensile strength. According to his theory, the tensile strength for a given material is a universal function of a reduced time or a reduced strain rate, except at short times or high strain rates where the material approaches glasslike behavior. Also, to superpose data measured at different temperatures, a shift factor is needed which is determined by the temperature dependence of the frictional factor for polymeric segment mobility and thus is the same factor as used to superpose viscoelastic data measured in small deformations. Thus, according to Bueche's theory, the temperature dependence of the tensile strength is given by the equation of Williams, Landel, and Ferry which is applicable in the temperature range Tg<T<(Tg+100). Bueche reported some tensile data for polybutyl methacrylate which has a glass transition temperature of 8° C. These tensile data were measured under various constant loads at temperatures between 30 and 95° C, and reasonable agreement between theory and experiment was found. Although Bueche did not consider the ultimate elongation, it seems reasonable that such data can be superposed by using the same shift factor as required to superpose the tensile strength data. Other workers have not considered explicitly the effect of viscous forces on the ultimate properties but have considered the effect of such variables as molecular weight, degree of crosslinking, and plasticizers.

2014 ◽  
Vol 1048 ◽  
pp. 36-40
Author(s):  
Wei Lai Chen ◽  
Lin Yan Wan ◽  
Hong Qin

Microstructures and mechanical properties of melt spinning spandex were studied in this article.Cross section and longitudinal surface were observed and analyzed by JSM-5610LV scanning electron microscopy. Q2000 DSC differential scanning calorimeter was used to test the glass transition temperature and melting temperature which indicated glass transition temperature is about 44°C and melting temperature is about 200°C. We employed JSM-5610LV scanning electron microscopy to observe adhesion of melt spinning spandex with nylon filament after different time and temperature processing. It concluded that after 150°C90s、160°C60s、160°C90s、170°C30s heat treatment, the adhesive of melt spinning spandex with nylon is good. At the same time,tensile strength and elastic properties of melt spinning spandex which was processed under different time and temperature were tested, tensile strength and elastic recovery of melt spinning spandex after160°C 90s heat treatment is the best.


2014 ◽  
Vol 904 ◽  
pp. 74-77 ◽  
Author(s):  
Qu Li ◽  
Heng Wu ◽  
Si Yuan Xie ◽  
Jiao Sun ◽  
Xing Hai Liu ◽  
...  

Biodegradable poly (propylene carbonate) (PPC) composite with a slight improvement in the thermal stability and tensile strength was successfully prepared by incorporating a low content of nano-SiO2. Tensile tests demonstrate the better mechanical properties of the composites prepared in this study. The obtained composites increases sharply from 1.57Mpa to 12.04Mpa by incorporating 5wt% nano-SiO2. Furthermore, the composites show approximately 8°C higher glass transition temperature (Tg) than that of neat PPC.The Tdmax of composite with 5wt% of nano-SiO2 was about 40°C higher than that of neat PPC.


2017 ◽  
Vol 873 ◽  
pp. 123-127
Author(s):  
Yupawan Thongjun ◽  
Thiti Kaisone ◽  
Pran Hanthanon ◽  
Chanon Wiphanurat ◽  
Sumate Ouipanich ◽  
...  

The aim of this study was to characterize thermoplastic starch containing corn starch and tapioca residues, which were used as reinforcement in a blended matrix. In the process, the composites were prepared with different tapioca residue contents at 20, 30, 40, 50 and 60 % by weight using compression molding at 135 °C for 8 min. Subsequently, their mechanical, thermal and morphology properties were evaluated. The results showed that the reinforcing effect of tapioca residue lead an increase in the stiffness of the samples. Young’s modulus increased with higher tapioca residue content. When the loading of tapioca residue increased tensile strength for 80/20 and 70/30 mixtures from 7.46 to 8.58 MPa. In addition to the highest of tapioca residue could increase tensile strength dramatically. Further, the glass transition temperature tended to decrease with the increased loading of tapioca residue. Moreover, the morphology showed that the increment of tapioca residue content appeared embedded in the polymer matrix.


Fibers ◽  
2021 ◽  
Vol 9 (1) ◽  
pp. 2
Author(s):  
Quoc Pham Le ◽  
Mayya V. Uspenskaya ◽  
Roman O. Olekhnovich ◽  
Mikhail A. Baranov

This paper investigates the mechanical properties of oriented polyvinyl chloride (PVC) nanofiber mats, which, were obtained by electrospinning a PVC solution. PVC was dissolved in a solvent mixture of tetrahydrofuran/dimethylformamide. Electrospinning parameters used in our work were, voltage 20 kV; flow rate 0.5 mL/h; the distance between the syringe tip and collector was 15 cm. The rotating speed of the drum collector was varied from 500 to 2500 rpm with a range of 500 rpm. Nanofiber mats were characterized by scanning electron microscope, thermogravimetric analysis, differential scanning calorimetry methods. The mechanical properties of PVC nanofiber mats, such as tensile strength, Young’s modulus, thermal degradation, and glass transition temperature were also analyzed. It was shown that, by increasing the collector’s rotation speed from 0 (flat plate collector) to 2500 rpm (drum collector), the average diameter of PVC nanofibers decreased from 313 ± 52 to 229 ± 47 nm. At the same time, it was observed that the mechanical properties of the resulting nanofiber mats were improved: tensile strength increased from 2.2 ± 0.2 MPa to 9.1 ± 0.3 MPa, Young’s modulus from 53 ± 14 to 308 ± 19 MPa. Thermogravimetric analysis measurements showed that there was no difference in the process of thermal degradation of nanofiber mats and PVC powders. On the other hand, the glass transition temperature of nanofiber mats and powders did show different values, such values were 77.5 °C and 83.2 °C, respectively.


Author(s):  
James Njuguna ◽  
Peter Muchiri ◽  
Nancy Karuri ◽  
Fredrick Madaraka Mwema ◽  
Michael T. Herzog ◽  
...  

This study aimed to determine the possible changes in thermo-mechanical properties between recycled polyurethane with benchmark polyurethane. The glycolysis polyol was used as a raw material for recycled polyurethane production. The glass transition temperature of the recycled polyurethane was determined using DSC. Tensile strength, elastic modulus, toughness, and hardness test of the recycled polyurethane were conducted at 24°C, 40°C, and 60°C. The glass transition temperatures for the recycled and the benchmark polyurethane occurred at 43°C and 50.4°C, respectively. Tensile strength for recycled polyurethane was lower than that of benchmark polyurethane by 29-43%. Recycled polyurethane recorded lower toughness than petroleum-based pure polyurethane by 13-16%. However, recycled polyurethane recorded high shored D values than the benchmark polyurethane by 9-29%. This study reveals that recycled polyol could be used as feedstock for polyurethane production with applications tailored to its mechanical properties.


2012 ◽  
Vol 626 ◽  
pp. 240-244
Author(s):  
Skulrat Pichaiyut ◽  
Charoen Nakason ◽  
Norbert Vennemann

Thermoplastic natural rubber (TPNR) based on blending of thermoplastic polyurethane (TPU) and epoxidized natural rubber with 25 mol % epoxide (ENR-25) was prepared by simple blend technique. Influence of different types of plasticizer and processing oil (i.e., DOP, TDAE oil and Paraffinic oil) with a fixed loading level of 20 phr was investigated. The main aim was to improve elasticity and lowering the hardness of the blends. It was found that an incorporation of processing oil and plasticizer caused decreasing of mixing torque, mixing temperature, and mechanical properties in terms of tensile strength, and hardness. This is attributed to diffusion of oil or plasticizer molecules into ENR and TPU phases. The oil and plasticizer typically acts as lubricant to promote the ease of flow and influence on various properties. It was also found that an incorporation of processing oil and plasticizer caused decreasing of glass transition temperature (Tg) of rubber and TPU phases, tension set value and Tan δ which refer to greater rubber elasticity and tendency to recover to original shape after prolonged extension. Additionally, the blend with DOP exhibited superior mechanical and other related properties than those of the blends with TDAE oil and paraffinic oil, respectively.


2021 ◽  
Vol 2 (2) ◽  
pp. 419-430
Author(s):  
Ankur Bajpai ◽  
James R. Davidson ◽  
Colin Robert

The tensile fracture mechanics and thermo-mechanical properties of mixtures composed of two kinds of epoxy resins of different chemical structures and functional groups were studied. The base resin was a bi-functional epoxy resin based on diglycidyl ether of bisphenol-A (DGEBA) and the other resins were (a) distilled triglycidylether of meta-amino phenol (b) 1, 6–naphthalene di epoxy and (c) fluorene di epoxy. This research shows that a small number of multifunctional epoxy systems, both di- and tri-functional, can significantly increase tensile strength (14%) over neat DGEBA while having no negative impact on other mechanical properties including glass transition temperature and elastic modulus. In fact, when compared to unmodified DGEBA, the tri-functional epoxy shows a slight increase (5%) in glass transition temperature at 10 wt.% concentration. The enhanced crosslinking of DGEBA (90 wt.%)/distilled triglycidylether of meta-amino phenol (10 wt.%) blends may be the possible reason for the improved glass transition. Finally, the influence of strain rate, temperature and moisture were investigated for both the neat DGEBA and the best performing modified system. The neat DGEBA was steadily outperformed by its modified counterpart in every condition.


Life ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 43
Author(s):  
Lamya Zahir ◽  
Takumitsu Kida ◽  
Ryo Tanaka ◽  
Yuushou Nakayama ◽  
Takeshi Shiono ◽  
...  

An innovative type of biodegradable thermoplastic elastomers with improved mechanical properties from very common and potentially renewable sources, poly(L-lactide)-b-poly(2-methyl-1,3-propylene glutarate)-b-poly(L-lactide) (PLA-b-PMPG-b-PLA)s, has been developed for the first time. PLA-b-PMPG-b-PLAs were synthesized by polycondensation of 2-methyl-1,3-propanediol and glutaric acid and successive ring-opening polymerization of L-lactide, where PMPG is an amorphous central block with low glass transition temperature and PLA is hard semicrystalline terminal blocks. The copolymers showed glass transition temperature at lower than −40 °C and melting temperature at 130–152 °C. The tensile tests of these copolymers were also performed to evaluate their mechanical properties. The degradation of the copolymers and PMPG by enzymes proteinase K and lipase PS were investigated. Microbial biodegradation in seawater was also performed at 27 °C. The triblock copolymers and PMPG homopolymer were found to show 9–15% biodegradation within 28 days, representing their relatively high biodegradability in seawater. The macromolecular structure of the triblock copolymers of PLA and PMPG can be controlled to tune their mechanical and biodegradation properties, demonstrating their potential use in various applications.


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