Poly(Dimethylsiloxane) Elastomers from Aqueous Emulsions: II. Mechanical Properties

1998 ◽  
Vol 71 (5) ◽  
pp. 928-940 ◽  
Author(s):  
J. E. Mark ◽  
D. W. McCarthy

Abstract Stress—strain measurements in simple uniaxial extension were used to characterize the mechanical properties of the elastomers prepared from poly(dimethylsilxoxane) emulsions as described in the preceding paper. The studies were carried out on the materials in the unswollen state, after they had received different treatments, specifically no aging, aging in the dry state, or aging in the wet (emulsion) state. Increase in silane crosslinker concentration was found to increase nominal stresses and moduli but to decrease extensibility, two changes that parallel the observed decreases in soluble polymer fractions and extents of equilibrium swelling reported earlier. The energy for rupture (“toughness”) frequently stays roughly constant because the decreased extensibility at least partially offsets the increased stresses. The changes in mechanical properties are due both to increased crosslinking and to reinforcing effects from silica generated from the silane, with the latter effect generally being the more important. The mechanical properties are much more affected by aging in the wet state, as opposed to aging in the dry state. For example, wet-aged elastomers generally had values of the nominal stress and modulus that were consistently lower than those for the unaged elastomers. Wet aging appears to be the result of the continual breaking and reforming of siloxane bonds in the aqueous environment of the emulsion, as probably accelerated by the presence of the tin catalyst.

1999 ◽  
Vol 72 (1) ◽  
pp. 138-151 ◽  
Author(s):  
Zhengcai Pu ◽  
James E. Mark ◽  
Gregory Beaucage

Abstract The reinforcing effects of zeolites in poly(dimethylsiloxane) (PDMS) elastomers were characterized using two preparative approaches. In the first, end-functionalized polymer chains were blended into the zeolite, and were then endlinked into the required network structure. The second approach represented an attempt to force some chains through the cavities, by blending the monomer itself into the zeolite and then polymerizing it to obtain the PDMS elastomer. The two types of zeolite-filled PDMS were characterized using stress-strain measurements in elongation, equilibrium swelling, and small-angle X-ray scattering. The second synthetic approach did seem to give improvements in mechanical properties, particularly when the average cavity size of the zeolite particles was relatively large. Ascribing the observed improvements in reinforcement at least partly to the threading of some PDMS chains through the zeolites was supported by the results obtained in the swelling and scattering experiments.


1992 ◽  
Vol 274 ◽  
Author(s):  
James E. Mark ◽  
Shuhong Wang ◽  
Ping Xu ◽  
Jianye Wen

ABSTRACTElastomeric networks prepared by tetrafunctionally end linking hydroxyl-terminated poly(dimethylsiloxane) chains (PDMS) were filled by the in-situ precipitation of silica. The resulting networks were investigated under uniaxial elongation, biaxial extension, shear, and torsion in order to characterize the resulting changes in mechanical properties. Compared with the unfilled networks, the silica-filled materials showed large reinforcing effects. Specifically, their values of the modulus, ultimate strength, and rupture energy increased significantly. The results thus indicate that the PDMS networks filled by the in-situ precipitation of silica have very good mechanical properties in several, rather different deformations. Examples of other deformations of interest are equilibrium swelling, and dynamic cycling for characterization of compression set.


Author(s):  
Inna Slepchuk ◽  
Olga Ya. Semeshko ◽  
Yuliya G. Saribekova ◽  
Irina N. Kulish ◽  
Igor V. Gorokhov

Results of study of influence of amount of functional groups of glycidyl ethers on characteristics of the spatial grid of crosslinked polyurethane polymer are presented. Parameters of a three-dimensional spatial grid of investigated samples of polymeric films and their physical and mechanical properties were determined by a method of equilibrium swelling in organic solvents.


Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2076 ◽  
Author(s):  
Rizacan Sarikaya ◽  
Linyong Song ◽  
Qiang Ye ◽  
Anil Misra ◽  
Candan Tamerler ◽  
...  

The inherent degradation property of most dental resins in the mouth leads to the long-term release of degradation by-products at the adhesive/tooth interface. The by-products increase the virulence of cariogenic bacteria, provoking a degradative positive-feedback loop that leads to physicochemical and mechanical failure. Photoinduced free-radical polymerization and sol‒gel reactions have been coupled to produce a novel autonomous-strengthening adhesive with enhanced hydrolytic stability. This paper investigates the effect of network structure on time-dependent mechanical properties in adhesives with and without autonomous strengthening. Stress relaxation was conducted under 0.2% strain for 8 h followed by 40 h recovery in water. The stress‒time relationship is analyzed by nonlinear least-squares data-fitting. The fitted Prony series predicts the sample’s history under monotonic loading. Results showed that the control failed after the first loading‒unloading‒recovery cycle with permanent deformation. While for the experimental sample, the displacement was almost completely recovered and the Young’s modulus increased significantly after the first test cycle. The experimental polymer exhibited higher degree of conversion, lower leachate, and time-dependent stiffening characteristics. The autonomous-strengthening reaction persists in the aqueous environment leading to a network with enhanced resistance to deformation. The results illustrate a rational approach for tuning the viscoelasticity of durable dental adhesives.


Polymers ◽  
2019 ◽  
Vol 11 (2) ◽  
pp. 275 ◽  
Author(s):  
Corinna Dannert ◽  
Bjørn Torger Stokke ◽  
Rita S. Dias

Hydrogels are materials used in a variety of applications, ranging from tissue engineering to drug delivery. The incorporation of nanoparticles to yield composite hydrogels has gained substantial momentum over the years since these afford tailor-making and extend material mechanical properties far beyond those achievable through molecular design of the network component. Here, we review different procedures that have been used to integrate nanoparticles into hydrogels; the types of interactions acting between polymers and nanoparticles; and how these underpin the improved mechanical and optical properties of the gels, including the self-healing ability of these composite gels, as well as serving as the basis for future development. In a less explored approach, hydrogels have been used as dispersants of nanomaterials, allowing a larger exposure of the surface of the nanomaterial and thus a better performance in catalytic and sensor applications. Furthermore, the reporting capacity of integrated nanoparticles in hydrogels to assess hydrogel properties, such as equilibrium swelling and elasticity, is highlighted.


1993 ◽  
Vol 311 ◽  
Author(s):  
A.Peter Jardine ◽  
Peter G. Mercado

ABSTRACTAlthough the thermo-mechanical properties of NiTi are well known for bulk material, its deposition and utilization as a thin film are still in their earliest stages of research. The deposition of thin-films of Shape Memory Effect NiTi onto Si(100) wafers offers several advantages over bulk NiTi, including fast response times and comparatively large transformation forces. This has made it a promising candidate material as micro-actuators for Micro-Electro-Mechanical (MEMS) systems as well as for strain measurements. The cycling time for actuation was measured for a 20 μm free standing NiTi thin film cantilever. It was demonstrated that cycling frequencies of up to 50 Hz are achievable.


Polymers ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 2020 ◽  
Author(s):  
Do Young Kim ◽  
Jae Woo Park ◽  
Dong Yun Lee ◽  
Kwan Ho Seo

The extreme elasticity and reversible deformability of rubber, which is one of the most versatile polymers in modern society, is dependent on several factors, including the processing conditions, curing system, and types of additives used. Since the rubber’s mechanical properties are influenced by the existing structural crosslinks, their correlation with the crosslink characteristics of rubber was investigated using the equilibrium swelling theory of the Flory–Rehner equation and the rubber–filler interaction theory of the Kraus equation. Herein, we examined whether the accelerator and reinforcement agent quantitatively contributed to chemical cross-linkages and rubber–filler interaction. In conclusion, the accelerator content supported the chemically crosslinked structures of the monosulfides and the disulfides in natural rubber (NR). Additionally, these results demonstrated that the mechanical properties and the thermal resistance of NR were dependent on the crosslink characteristics. The findings of this study provide an insight into the development and application of NR products for the mechanical optimization of rubber-based products.


2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Suzana Samaržija-Jovanović ◽  
Vojislav Jovanović ◽  
Gordana Marković ◽  
Ivana Zeković ◽  
Milena Marinović-Cincović

Opalized white tuff (OWT) with 40 μm average particle size and 39.3 m2/g specific surface area has been introduced into polyisoprene rubber (NR). Their reinforcing effects were evaluated by comparisons with those from precipitated silica (PSi). The cure characteristic, apparent activation energy of cross-link (Eac) and reversion (Ear), and mechanical properties of a variety of composites based on these rubbers were studied. This was done using vulcanization techniques, mechanical testing, and scanning electron microscopy (SEM). The results showed that OWT can greatly improve the vulcanizing process by shortening the time of optimum cure (tc90) and the scorch time (ts2) of cross-linked rubber composites, which improves production efficiency and operational security. The rubber composites filled with 50 phr of OWT were found to have good mechanical and elastomeric properties. The tensile strengths of the NR/OWT composites are close to those of NR/PSi composites, but the tear strength and modulus are not as good as the corresponding properties of those containing precipitated silica. Morphology results revealed that the OWT is poorly dispersed in the rubber matrix. According to that, the lower interactions between OWT and polyisoprene rubber macromolecules are obtained, but similar mechanical properties of NR/OWT (100/50) rubber composites compared with NR/PSi (100/50) rubber composites are resulted.


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