Tensile and tearing

Combination Flame Retardant—Durable Press Performance. Systems using THPC, urea, and TMM can be formulated to give fabrics which combine both flame-retardant performance and increased wrinkle recovery values (80). Another system employs dimethylol cyanoguanidine with THPC under acidic conditions (115). Both of these systems lead to substantial losses in fabric tensile and tearing strength. 

Thiokol elastomers possess fairly low tensile and tear properties. However, they have exceUent resistance to both aHphatic and aromatic solvents at room temperature and slightly elevated temperatures. The Thiokol division of Morton International Corporation is the suppHer of polysulftde elastomers in the United States. It is estimated that 1360—1600 t are used aimually in the United States. The primary use of polysulftde is in seals, gaskets, roUs, and diaphragms where solvent resistance and low permeabiHty are useful. 

Vinyl Acetate—Ethylene Copolymers. In these random copolymers, the ratio of ethylene to vinyl acetate (EVA) is varied from 30—60%. As the vinyl acetate content increases, the oil and heat resistance increases. With higher ethylene content the physical strength, tensile, and tear increases. The polymers are cured with peroxide. The main properties of these elastomers include heat resistance, moderate oil and solvent resistance, low compression set, good weather resistance, high damping, exceUent o2one resistance, and they can be easily colored (see Vinyl polymers, poly(VINYL acetate)). 

Conventional cure systems use relatively high levels (2.5 + phr) of sulfur combkied with lower levels of accelerator(s). These typically provide high initial physical properties, tensile and tear strengths, and good initial fatigue life, but with a greater tendency to lose these properties after heat aging. 

In general, however, the vulcanizates suffer from poor low temperature crystallization performance compared to a conventional sulfur cure, and also have inferior tensile and tear properties. Urethane cross-linking systems (37), eg, Novor 950 (see Table 3) are also extremely heat resistant, but exhibit inferior tensile and dynamic properties compared to conventional sulfur-cured vulcanizates. One added virtue is that they can be used in conjunction with sulfur systems to produce an exceUent compromise according to the ratios used (38). 

Polymers can be modified by the introduction of ionic groups [I]. The ionic polymers, also called ionomers, offer great potential in a variety of applications. Ionic rubbers are mostly prepared by metal ion neutralization of acid functionalized rubbers, such as carboxylated styrene-butadiene rubber, carboxylated polybutadiene rubber, and carboxylated nitrile rubber 12-5]. Ionic rubbers under ambient conditions show moderate to high tensile and tear strength and high elongation. The ionic crosslinks are thermolabile and, thus, the materials can be processed just as thermoplastics are processed [6]. 

Elastomeric composition for dynamic application of cross-linked E-plastomers has been made with filer-reinforced systems which contain a metal salt (typically zinc) of an alpha, beta unsaturated acid. These additives improve the tensile and tear strength of the elastomer and are cured with a peroxide cure system. These cross-linked articles are suitable for dynamic loading applications such as belting, including power transmission and flat belting. 

The carboxylated types (XNBR) contain one, or more, acrylic type of acid as a terpolymer, the resultant chain being similar to nitrile except for the presence of carboxyl groups which occur about every 100 to 200 carbon atoms. This modification gives the polymer vastly improved abrasion resistance, higher hardness, higher tensile and tear strength, better low temperature brittleness, and better retention of physical properties after hot-oil and air ageing when compared to ordinary nitrile rubber. 

PVC/NBR polymer blends can be produced as colloidal or mechanical blends, the former generally giving superior properties. Commercially available blends have PVC contents ranging from 30-55%. The blends have reduced elasticity, which gives improved extrudability, but they also exhibit superior ozone resistance, improved oil swell resistance, and tensile and tear strength this, however, is achieved at the expense of low temperature flexibility and compression set. The ozone resistance of such blends is, however, only improved if the PVC is adequately distributed and fluxed. This is harder to achieve in mechanical blends, but if it is not achieved failure due to ozone attack can occur. 

The polyurethane formulation Involved a proprietary crossllnkable system based on poly(propylene glycol) and methylene dllsocyanate (NCO/OH ratio = 1.0). For studies of viscoelastic, energy absorption, and fatigue behavior, the weight fractions of PUMA were 0, 0.25, 0.50, 0.75, and 1.0 for studies of tensile and tear strength, the ratios were 0, 0.10, 0.20, 0.25, 0.30, and 0.40. Reactants were mixed at room temperature, degassed, poured Into a mold, and cured at 60 C for 48 hr. 

Tensile and tear strengths were determined using ASTM standards D412 and D1004, respectively, at a crosshead speed of 0.42 mm/s (1 In/mln) values reported are the average for 3 specimens. The elastic and Inelastic (plastic) components of the total elongation... 

Tensile and Tearing Behavior. As shown in Figure 4, the tensile and tear strengths increased with increasing PMMA content measurements of tear strength were not feasible at PMMA contents > 30%. In any case, the incorporation of PMMA at even relatively low levels greatly improves the rather low strengths of the unmodified PU. 

Figure 4. Tensile and tear strength of FU/FMMA SlNs as a function of composition.

Regardless of the method of cross-linking, mechanical properties of a cross-linked elastomer depend on cross-link density. Modulus and hardness increase monotonically with cross-link density, and at the same time, the network becomes more elastic. Fracture properties, i.e., tensile and tear strength, pass through a maximum as the cross-link density increases (see Figure 5.4). 

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