Polyolefins mechanism

The optimum processing temperature for Solanyl is lower than those of synthetic plastics. The recommended temperature profile ranges from about 110 °C at the first heated zone to 170 °C at the nozzle. Solanyl has excellent flow properties enabling low wall thickness. However, the injection pressure is about 20-30% higher than needed for polyolefins. Mechanical properties are roughly in the same order of magnitude as polyethylene and polystyrene. 

Initiation of polyolefin mechanical degradation increases with the applied stress [33], yet the effect is pronounced if a limit of stress is exceeded and for a deformation of 5-12%. 

Hawkins W L, The thermal oxidation of polyolefins — mechanisms of degradation and stabilization in Geuskens G, Degradation and Stabilization of Polymers, London, Applied Science, 77—94, 1975. 

In order for a soHd to bum it must be volatilized, because combustion is almost exclusively a gas-phase phenomenon. In the case of a polymer, this means that decomposition must occur. The decomposition begins in the soHd phase and may continue in the Hquid (melt) and gas phases. Decomposition produces low molecular weight chemical compounds that eventually enter the gas phase. Heat from combustion causes further decomposition and volatilization and, therefore, further combustion. Thus the burning of a soHd is like a chain reaction. For a compound to function as a flame retardant it must intermpt this cycle in some way. There are several mechanistic descriptions by which flame retardants modify flammabiUty. Each flame retardant actually functions by a combination of mechanisms. For example, metal hydroxides such as Al(OH)2 decompose endothermically (thermal quenching) to give water (inert gas dilution). In addition, in cases where up to 60 wt % of Al(OH)2 may be used, such as in polyolefins, the physical dilution effect cannot be ignored. 

Degradation of polyolefins such as polyethylene, polypropylene, polybutylene, and polybutadiene promoted by metals and other oxidants occurs via an oxidation and a photo-oxidative mechanism, the two being difficult to separate in environmental degradation. The general mechanism common to all these reactions is that shown in equation 9. The reactant radical may be produced by any suitable mechanism from the interaction of air or oxygen with polyolefins (42) to form peroxides, which are subsequentiy decomposed by ultraviolet radiation. These reaction intermediates abstract more hydrogen atoms from the polymer backbone, which is ultimately converted into a polymer with ketone functionahties and degraded by the Norrish mechanisms (eq. 

Fabrics composed of synthetic polymer fibers are frequendy subjected to heat-setting operations. Because of the thermoplastic nature of these fibers, eg, polyester, nylon, polyolefins, and triacetate, it is possible to set such fabrics iato desired configurations. These heat treatments iavolve recrystaUization mechanisms at the molecular level, and thus are permanent unless the fabrics are exposed to thermal conditions more severe than those used ia the heat-setting process. 

The mechanism by which the primers are thought to work is relatively straightforward. The primer first diffuses into the polyolefin surface, and subsequently becomes entangled in the polyolefin. The primer molecule can then act as an anchor in the substrate surface for the adhesive polymer, which forms after the primer initiates polymerization of the alkyl cyanoacrylate monomer [37]. 

Oridation. This is caused by contact with oxidising acids, exposure to u-v, prolonged application of excessive heat, or exposure to weathering. It results in a deterioration of mechanical properties (embrittlement and possibly stress cracking), increase in power factor, and loss of clarity. It affects most thermoplastics to varying degrees, in particular polyolefins, PVC, nylons, and cellulose derivatives. 

The synthesis of new polymeric materials having complex properties has recently become of great practical importance to polymer chemistry and technology. The synthesis of new materials can be prepared by either their monomers or modification of used polymers in industry. Today, polystyrene (PS), which is widely used in industrial applications as polyolefins and polyvinylchlorides, is also used for the production of plastic materials, which are used instead of metals in technology. For this reason, it is important to synthesize different PS plastic materials. Among the modification of PS, two methods can be considered, viz. physical and chemical modifications. These methods are extensively used to increase physico-mechanical properties, such as resistance to strike, air, or temperature for the synthesizing of new PS plastic materials. 

The reactive compatibilization of HDPE-NBR and PP-NBR blends has been studied by Thomas and coworkers [75,76]. The maleic anhydride modified polyolefins and phenolic modified polyolefins are used as com-patibilizers. The effect of the concentration of these compatibilizers on the compatibility of these blends was investigated in terms of morphology and mechanical properties. It was found that in these blends an optimum quantity of the compatibilizer was required to obtain maximum improvement in properties, and after that a leveling off was observed. The domain size of the dispersed NBR phase in these blends is decreased up to a certain level and then increases (Fig. 12 and 13). The reduction in domain size is attributed to the increase in... 

The mechanical properties of these blends are also increased with an increase in compatibilizer concentration. The improvement in tensile strength and tear strength on the addition of modified polyolefins are shown in Fig. 15. The mechanical properties also show a leveling off after the optimum concentration. The im-... 

Currently, all commercially available, spirally wound lithium-ion cells use microporous polyolefin separators. In particular, separators are made from polyethylene, polypropylene, or some combination of the two. Polyolefins provide excellent mechanical properties and chemical stability at a reasonable cost. A number of manufacturers produce microporous polyolefin separators (Table 1.)... 

---