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Dynamical Mechanical Properties

The mechanical relaxations in polymers correspond to particular mechanisms of thermally activated molecular motion and therefore to general mobility of polymer chains. Depending on their nature, polymers deform differently. Thermosetting polymers usually have little chain mobility and fail in a brittle manner. On the other hand, the chains move freely in thermoplastics and the polymer can yield or deform homogeneously at higher temperatures and behave as a viscoelastic-plastic solid [165]. [Pg.362]

Well-dispersed nanofillers constrain the polymer chains and their interactions confer rigidity to the nanocomposite [33]. The interactions are [Pg.362]

High addition of nanofillers can adversely affect the properties of the nanocomposites due to the poor dispersion of nanofillers throughout the polymer matrix and weak adhesive bonding with the polymer matrix [Pg.363]

An increase in the crystallinity [77,133,137] or interfacial crystallinity have been considered other parameters for improving the mechanical response of polymers [170]. Oxidized NDs effectively enhanced the crystallization ability of PVA, indicating the crystalline regions may act as physical crosslinks or filler particles. The increased crystallinity and reinforcing effect of oxidized NDs increased the storage modulus of all the PVA nanocomposites to a higher degree than that of neat PVA [48]. Sahoo [Pg.367]


The dynamic mechanical properties of PTFE have been measured at frequencies from 0.033 to 90 Uz. Abmpt changes in the distribution of relaxation times are associated with the crystalline transitions at 19 and 30°C (75). The activation energies are 102.5 kj/mol (24.5 kcal/mol) below 19°C, 510.4 kJ/mol (122 kcal/mol) between the transitions, and 31.4 kJ/mol (7.5 kcal/mol) above 30°C. [Pg.351]

Fatty Acid Process. When free fatty acids are used instead of oil as the starting component, the alcoholysis step is avoided. AH of the ingredients can therefore be charged into the reactor to start a batch. The reactants are heated together, under agitation and an inert gas blanket, until the desired endpoint is reached. Alkyds prepared by the fatty acid process have narrower molecular weight distribution and give films with better dynamic mechanical properties (34). [Pg.38]

Determining and Reporting Dynamic Mechanical Properties of Plastics... [Pg.197]

Using physical properties relating to performance parameters leads to the development of algorithms for predicting performance for laboratory screening of potential improvements. Many of these algorithms have been estabUshed. The two main categories of measurement criteria are quasi static and dynamic mechanical properties. [Pg.251]

The dynamic mechanical properties of VDC—VC copolymers have been studied in detail. The incorporation of VC units in the polymer results in a drop in dynamic modulus because of the reduction in crystallinity. However, the glass-transition temperature is raised therefore, the softening effect observed at room temperature is accompanied by increased brittleness at lower temperatures. These copolymers are normally plasticized in order to avoid this. Small amounts of plasticizer (2—10 wt %) depress T significantly without loss of strength at room temperature. At higher levels of VC, the T of the copolymer is above room temperature and the modulus rises again. A minimum in modulus or maximum in softness is usually observed in copolymers in which T is above room temperature. A thermomechanical analysis of VDC—AN (acrylonitrile) and VDC—MMA (methyl methacrylate) copolymer systems shows a minimum in softening point at 79.4 and 68.1 mol % VDC, respectively (86). [Pg.434]

The presence of three oxyethylene units in the spacer of PTEB slows down the crystallization from the meso-phase, which is a very rapid process in the analogous polybibenzoate with an all-methylene spacer, P8MB [13]. Other effects of the presence of ether groups in the spacer are the change from a monotropic behavior in P8MB to an enantiotropic one in PTEB, as well as the reduction in the glass transition temperature. This rather interesting behavior led us to perform a detailed study of the dynamic mechanical properties of copolymers of these two poly bibenzoates [41]. [Pg.396]

Measurement of dynamic mechanical properties was carried out under tension mode using a viscoelasto-meter, (Rheovibron DDV-III-EP, M/s, Orientec Corp., Tokyo, Japan). Sample size was 3.5 cm x 6.5 mm x 2 mm. Testing was carried out at a low amplitude, 0.025 mm, over a temperature range of - 100°C to +200°C. Heating rate was TC/min and frequency of oscillation was 3.5 Hz or 110 Hz. [Pg.442]

Torsion property As noted, the shear modulus is usually obtained by using pendulum and oscillatory rheometer techniques. The torsional pendulum (ASTM D 2236 Dynamic Mechanical Properties of Plastics by Means of a Torsional Pendulum Test Procedure) is a popular test, since it is applicable to virtually all plastics and uses a simple specimen readily fabricated by all commercial processes or easily cut from fabricated products. [Pg.62]

Interest in the use of syntactic foam as a shock attenuator led to studies of its static and dynamic mechanical properties. Particularly important is the influence of loading rate on stiffness and crushing strength, since oversensitivity of either of these parameters can complicate the prediction of the effectiveness of a foam system as an energy absorber. [Pg.501]

Finer dispersion of silica improves the mechanical and dynamic mechanical properties of the resultant composites. Figure 3.11a and b compares the tensile properties of the acrylic copolymer and terpolymers in the uncross-hnked and cross-linked states, respectively. [Pg.68]

Adsorption of rubber over the nanosilica particles alters the viscoelastic responses. Analysis of dynamic mechanical properties therefore provides a direct clue of the mbber-silica interaction. Figure 3.22 shows the variation in storage modulus (log scale) and tan 8 against temperature for ACM-silica, ENR-silica, and in situ acrylic copolymer and terpolymer-silica hybrid nanocomposites. [Pg.77]

Recently Sahoo and Bhowmick [75] synthesized hydroxyl-terminated POSS in their laboratory starting from (3-aminopropyl) triethoxysilane (APS) and phenylglycidylether (PGE) and used it as a curative in carboxylated nitrile mbber (XNBR). This has been a newer class of material where the nanofiller simultaneously cures the mbber and promotes solvent resistance, as well as mechanical and dynamic mechanical properties. Table 3.3 illustrates some of these findings. [Pg.84]

Dynamic mechanical properties of the nanocomposites are shown in Figure 4.6. There is 10% improvement of the storage modulus at 20°C by incorporating only 4 wt% of the nanombe. [Pg.92]

ZnO nanoparticles possess greater surface/volume ratio. When used in carboxylated nitrile rubber as curative, ZnO nanoparticles show excellent mechanical and dynamic mechanical properties [41]. The ultimate tensile strength increases from 6.8 MPa in ordinary rabber grade ZnO-carboxylated nitrile rubber system to 14.9 MPa in nanosized ZnO-carboxylated nitrile mbber without sacrificing the elongation at failure values. Table 4.1 compares these mechanical properties of ordinary and nano-ZnO-carboxylated nitrile rubbers, where the latter system is superior due to more rubber-ZnO interaction at the nanolevel. [Pg.94]

Zhou L.L. and Eisenberg A., lonomeric blends. II. Compatibility and dynamic mechanical properties of sulfonated cis-l,4-polyisoprenes and styrene/4-vinylpyridine copolymer blends, J. Polym. Sci., Polym. Phy., 21, 595, 1983. [Pg.163]

Research concerning nylon-elastomer blends has mostly focused on the improvement of mechanical and thermal properties. Their dynamic mechanical properties are quite important both for processing and engineering applications. Wang and Zheng have smdied the influence of grafting on the dynamic mechanical properties of a blend based on nylon 1212 and a graft... [Pg.337]

The formation of PPD groups on the polymer backbone provides a mechanism to improve the polymer-filler interactions. The nitrogen-hydrogen bonds are capable of hydrogen bonding with polar groups on the surface of the filler. This enhanced interaction provides for somewhat unique dynamic mechanical properties. Under ideal conditions rolling resistance improves when QDI is used in the mix. Also, abrasion characteristics are maintained and in some cases even modest improvements occur. [Pg.496]

Mooney Viscometer studies at 100°C and 120°C show lower viscosity of the Al-hlled gums. Lower viscosity compounds require less energy input for extrusion. Comparative results on the dynamic mechanical properties, measured using a rubber process analyzer (RPA), show that at the... [Pg.510]

The B-series of silica samples were also blended with rubber and the compound formulation is shown in Table 17.6. The uncured gums were then tested according to ISO 5794-2 1998. The uncured samples were tested using a Mooney viscometer and an RPA, which measures the dynamic mechanical properties as the samples cure. Figure 17.7 shows the results of these two tests for the Mooney viscosity at 100°C, storage modulus, loss modulus, and tan 8. [Pg.512]


See other pages where Dynamical Mechanical Properties is mentioned: [Pg.329]    [Pg.236]    [Pg.49]    [Pg.485]    [Pg.500]    [Pg.212]    [Pg.213]    [Pg.214]    [Pg.145]    [Pg.392]    [Pg.473]    [Pg.572]    [Pg.669]    [Pg.102]    [Pg.187]    [Pg.252]    [Pg.216]    [Pg.201]    [Pg.157]    [Pg.248]    [Pg.44]    [Pg.116]    [Pg.148]    [Pg.196]    [Pg.317]    [Pg.317]    [Pg.367]    [Pg.435]    [Pg.489]   


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