Tensile superior

Heteroatom functionalized terpene resins are also utilized in hot melt adhesive and ink appHcations. Diels-Alder reaction of terpenic dienes or trienes with acrylates, methacrylates, or other a, P-unsaturated esters of polyhydric alcohols has been shown to yield resins with superior pressure sensitive adhesive properties relative to petroleum and unmodified polyterpene resins (107). Limonene—phenol resins, produced by the BF etherate-catalyzed condensation of 1.4—2.0 moles of limonene with 1.0 mole of phenol have been shown to impart improved tack, elongation, and tensile strength to ethylene—vinyl acetate and ethylene—methyl acrylate-based hot melt adhesive systems (108). Terpene polyol ethers have been shown to be particularly effective tackifiers in pressure sensitive adhesive appHcations (109). 

In order to achieve the desired fiber properties, the two monomers were copolymerized so the final product was a block copolymer of the ABA type, where A was pure polyglycoHde and B, a random copolymer of mostly poly (trimethylene carbonate). The selected composition was about 30—40% poly (trimethylene carbonate). This suture reportedly has exceUent flexibiHty and superior in vivo tensile strength retention compared to polyglycoHde. It has been absorbed without adverse reaction ia about seven months (43). MetaboHsm studies show that the route of excretion for the trimethylene carbonate moiety is somewhat different from the glycolate moiety. Most of the glycolate is excreted by urine whereas most of the carbonate is excreted by expired CO2 and uriae. 

The excellent chemical resistance and physical properties of PVA resins have resulted in broad industrial use. The polymer is an excellent adhesive and possesses solvent-, oil-, and grease-resistant properties matched by few other polymers. Poly(vinyl alcohol) films exhibit high tensile strength, abrasion resistance, and oxygen barrier properties which, under dry conditions, are superior to those of any other known polymer. The polymer s low surface tension provides for excellent emulsification and protective coUoid properties. 

Polycarbonates with superior notched impact strength, made by reacting bisphenol A, bis-phenol S and phosgene, were introduced in 1980 (Merlon T). These copolymers have a better impact strength at low temperatures than conventional polycarbonate, with little or no sacrifice in transparency. These co-carbonate polymers are also less notch sensitive and, unlike for the standard bis-phenol A polymer, the notched impact strength is almost independent of specimen thickness. Impact resistance increases with increase in the bis-phenol S component in the polymer feed. Whilst tensile and flexural properties are similar to those of the bis-phenol A polycarbonate, the polyco-carbonates have a slightly lower deflection temperature under load of about 126°C at 1.81 MPa loading. 

To improve the end use performance and make the processability easy, control of MW and MWD as well as the use of.more than one comonomer has been reported for LLDPE [28]. Union Carbide s high MW-LLDPE with broad MWD is a 1-hexene-based resin, and its film provides superior (about 30-50% higher) tensile strength, puncture resistance, and dart impact strength than conventional 1-hexene-based resin, but with lower tear resistance in the transverse direction. The broad MWD makes the resin processability easy on the conventional extruder. 

Use of 4-methylpentene-l comonomer with ethylene provides LLDPE resin have film properties (i.e., tensile strength, modulus, transverse direction tear strength, and impact strength) superior to 1-butene-based LLDPE resin as has been claimed by B.P. Chemicals. 1-Butene has also been used as the second comonomer with 4-methylpentene-l to tailor the properties of LLDPE resin [28], The properties of 4-methylpentene-l-based LLDPE film are given in Table 4. 

Amorphous polyarylates are light-amber transparent materials which exhibit mechanical properties comparable to that of unfilled PET in terms of tensile or flexural strength and modulus (Table 2.13) but are notably superior in terms of heat resistance (HDT = 174°C vs. 85°C for PET) and impact strength. 

Figure 3.17 shows the mechanical properties of the ACM-silica and ENR-silica hybrid composites synthesized from various pH, reproduced from the data reported by Bandyopadhyay et al. [36]. As morphology indicates, all the samples prepared within the pH range 1.0-2.0 are transparent, contain nanosilica particles, and are superior in tensile strength and modulus... 

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. 

Better cross-linking with the latter also improves post Tg viscoelastic responses of the rubber vulcanizates. Similar effect has also been observed with polychloroprene as investigated by Sahoo and Bhowmick [41]. Figure 4.8 represents the comparative tensile stress-strain behavior of polychloroprene rubber (CR) vulcanizates, highlighting superiority of the nanosized ZnO over conventional rubber grade ZnO [41]. 

Nylon-6-clay nanocomposites were also prepared by melt intercalation process [49]. Mechanical and thermal testing revealed that the properties of Nylon-6-clay nanocomposites are superior to Nylon. The tensile strength, flexural strength, and notched Izod impact strength are similar for both melt intercalation and in sim polymerization methods. However, the heat distortion temperature is low (112°C) for melt intercalated Nylon-6-nanocomposite, compared to 152°C for nanocomposite prepared via in situ polymerization [33]. 

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. 

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