Polypropylene linear

The propagating polymer then terminates, producing an isotactic polypropylene. Linear polyethylene occurs whether the reaction takes place by insertion through this sequence or, as explained earlier, by ligand occupation of any available vacant site. This course, however, results in a syndiotactic polypropylene when propylene is the ligand. 

Fig. 4. Polypropylene. Linear relation between extensional compliance and...

Figure 6.29. Infrared curves of (1) polypropylene-linear polyethylene blend, (2) ethylene-propylene copolymer rubber, (3) propylene-ethylene polyallomer. (Hagenmeyer and Edwards, 1966.)...

Most amorphous polymers linearly shrink about 0.4-0.6%. Crystalline polymers such as high density polyethylene and polypropylene linearly shrink about 2.0% (42). Thermoformed parts shrink away from female molds and onto male molds. Male molds must have typical draft angles of 2-5°, but sufficiently great enough to allow release of the formed parts. Female molds need minimal, if any, draft angles. 

Keywords Activation ansa-Zirconocene catalysts Constrained-geometiy catalysts ethene/propene rubbers Isotactic polypropylene Linear low-density polyethylene Molar-mass distribution Olefin polymerization Reaction... 

Type of membrane thin damp proof membranes (DPMs) are usually made of low density polyethylene (LDPE) and will have a greater risk of defects than specific gas-resistant membranes manufactured from more robust materials (polypropylene, linear low density polyethylene and high density polyethylene). As the strength and puncture resistance decrease the probability of defects increases For thin DPM material increase probability of failure defects 2000 g-200% 1200 g 00% 1000 g-600% Note these values do not apply to specific gas resistant membranes made from more robust materials than DPMs... 

Ethyne Acetal, Homopolymer (POM Homopolymer) Linear Low Density Polyethylene (LLDPE) Low Density Polyethylene (LDPE) Nylon 12 (PA 12) Nylon 46 (PA 46) Nylon 6 (PA 6) Nylon 610 (PA 610) Nylon 66 (PA 66) Polyamide, Nylon Polycaprolactones Polyethylene Polyethylene Terephthalate (PET) Polyethylene, HDPE Polypropylene Linear Low Density Polyethylene (LLDPE) 9... 

The latest of three ethylene recovery plants was started in 1991. Sasol sold almost 300,000 t of ethylene in 1992. Sasol also produces polypropylene at Secunda from propylene produced at Sasol Two. In 1992 Sasol started constmction of a linear alpha olefin plant at Secunda to be completed in 1994 (40). Initial production is expected to be 100,000 t/yr pentene and hexene. Sasol also has a project under constmction to extract and purify krypton and xenon from the air separation plants at Sasol Two. Other potential new products under consideration at Sasol are acrylonitrile, acetic acid, acetates, and alkylamines. 

Extmsion of polyethylene and some polypropylenes is usually through a circular die into a tubular form, which is cut and collapsed into flat film. Extmsion through a linear slot onto chilled rollers is called casting and is often used for polypropylene, polyester, and other resins. Cast, as well as some blown, films may be further heated and stretched in the machine or in transverse directions to orient the polymer within the film and improve physical properties such as tensile strength, stiffness, and low temperature resistance. 

Alkenylsuccinic anhydrides made from several linear alpha olefins are used in paper sizing, detergents, and other uses. Sulfosuccinic acid esters serve as surface active agents. Alkyd resins (qv) are used as surface coatings. Chlorendric anhydride [115-27-5] is used as a flame resistant component (see Flame retardants). Tetrahydrophthalic acid [88-98-2] and hexahydrophthalic anhydride [85-42-7] have specialty resin appHcations. Gas barrier films made by grafting maleic anhydride to polypropylene [25085-53-4] film are used in food packaging (qv). Poly(maleic anhydride) [24937-72-2] is used as a scale preventer and corrosion inhibitor (see Corrosion and corrosion control). Maleic anhydride forms copolymers with ethylene glycol methyl vinyl ethers which are partially esterified for biomedical and pharmaceutical uses (189) (see Pharmaceuticals). 

The majority of spunbonded fabrics are based on isotactic polypropylene and polyester (Table 1). Small quantities are made from nylon-6,6 and a growing percentage from high density polyethylene. Table 3 illustrates the basic characteristics of fibers made from different base polymers. Although some interest has been seen in the use of linear low density polyethylene (LLDPE) as a base polymer, largely because of potential increases in the softness of the final fabric (9), economic factors continue to favor polypropylene (see OlefinPOLYMERS, POLYPROPYLENE). 

Similarly, the random introduction by copolymerization of stericaHy incompatible repeating unit B into chains of crystalline A reduces the crystalline melting point and degree of crystallinity. If is reduced to T, crystals cannot form. Isotactic polypropylene and linear polyethylene homopolymers are each highly crystalline plastics. However, a random 65% ethylene—35% propylene copolymer of the two, poly(ethylene- (9-prop5lene) is a completely amorphous ethylene—propylene mbber (EPR). On the other hand, block copolymers of the two, poly(ethylene- -prop5iene) of the same overall composition, are highly crystalline. X-ray studies of these materials reveal both the polyethylene lattice and the isotactic polypropylene lattice, as the different blocks crystallize in thek own lattices. 

In the early 1950s, Ziegler observed that certain heterogeneous catalysts based on transition metals polymerized ethylene to a linear, high density material at modest pressures and temperatures. Natta showed that these catalysts also could produce highly stereospecific poly-a-olefins, notably isotactic polypropylene, and polydienes. They shared the 1963 Nobel Prize in chemistry for their work. 

Polybutadiene and polyunsaturated fats, which contain aHyUc hydrogen atoms, oxidize more readily than polypropylene, which contains tertiary hydrogen atoms. A linear hydrocarbon such as polyethylene, which has secondary hydrogens, is the most stable of these substrates. 

LDPE = low density polyethylene LLDPE = linear low density polyethylene HDPE = high density polyethylene PP = polypropylene PVC = polyvinyl chloride PS = polystyrene ABS = polyacrylonitrile-butadiene-styrene. 

Resins and plastics such as low-density polyethylene (LDPE), high-density polyethylene (HOPE), linear low-density polyethylene (LLDPE), polypropylene, polystyrene, and polyvinyl chloride (PVC) ... 

Polymerizations catalyzed with coordination compounds are becoming more important for obtaining polymers with special properties (linear and stereospecific). The first linear polyethylene polymer was prepared from a mixture of triethylaluminum and titanium tetrachloride (Ziegler catalyst) in the early 1950s. Later, Natta synthesized a stereoregular polypropylene with a Ziegler-type catalyst. These catalyst combinations are now called Zieglar-Natta catalysts. 

Ziegler-Natta catalysts currently produce linear polyethylene (non-branched), stereoregular polypropylene, cis-polybutadiene, and other stereoregular polymers. 

Polyethylene Low density Linear low density Medium density High density Polypropylene Polystyrene General purpose Impact... 

Applied stress There are TPs that will craze or crack under certain environmental condition. Products that are highly stressed mechanically must be checked very carefully. Polypropylene, ionomer, chlorinated polyether, phenoxy, EVA, and linear polyethylene are examples that offer greater freedom from stress crazing than some other TPs. Solvents may crack products held under stress. TSs is generally preferable for products under continuous loads. 

The most spectacular case of products arising from a catalyst invention is that of the stereospecific hydrocarbon polymers made possible by the Ziegler-Natta work on aluminum alkyl/transition metal halide combinations around 1950. Until these catalysts existed, polypropylene, polyiso-prene, and cis-polybutadiene could not be made, and linear polyethylene could not be made cheaply. For each of these products, very large investments were needed in big plants and in market development before they were competitive with the established, big thermoplastics and rubbers. Entrance fees ran into tens of millions of dollars. 

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