High-density polyethylene structural properties

Even with the same monomer, the properties of a polymer can vary significantly depending on how it is prepared. Free-radical polymerization of ethylene gives low-density polyethylene coordination polymerization gives high-density polyethylene. The properties are different because the structures are different, and the difference in the structures comes from the mechanisms by which the polymerizations take place. Free-radical polymerization of ethylene gives a branched polymer, coordination polymerization gives a linear one. 

The most common backbone structure found in commercial polymers is the saturated carbon-carbon structure. Polymers with saturated carbon-carbon backbones, such as polyethylene, polypropylene, polystyrene, polyvinyl chloride, and polyacrylates, are produced using chain-growth polymerizations. The saturated carbon-carbon backbone of polyethylene with no side groups is a relatively flexible polymer chain. The glass transition temperature is low at -20°C for high-density polyethylene. Side groups on the carbon-carbon backbone influence thermal transitions, solubility, and other polymer properties. 

Morpholine chromate, molecular formula, properties, and uses, 6 562t Morphology. See also Structure of carbon fibers, 26 737-739 of high density polyethylene, 20 162 of polymer blends, 20 356 of polymer colloid, 20 386-388 of PVC particles, 25 658-661, 661-663, 664-665... 

Low- and high-density polyethylene, polypropene, and polymers of other alkene (olefin) monomers constitute the polyolefin family of polymers. All except LDPE are produced by coordination catalysts. Coordination catalysts are also used to produce linear low-density polyethylene (LLDPE), which is essentially equivalent to LDPE in structure, properties, and applications (Sec. 8-1 lc). The production figures given above for LDPE do not include LLDPE. The production of LLDPE now exceeds that of LDPE, with about 10 billion pounds produced in 2001 in the United States. (Copolymers constitute about one-quarter of all low density polyethylenes see Sec. 6-8b.)... 

A test set of 6 to 13 aroma compound partition coefficients between different food contact polymers (low density polyethylene (LDPE), high density polyethylene (HDPE) polypropylene (PP), polyethylene terephthalate (PET), polyamide (PA)) and different food simulant phases (water, ethanol, aqueous ethanol/water mixtures, methanol, 1-propanol) were taken from the literature (Koszinowski and Piringer, 1989, Baner, 1992, Franz, 1990, Koszinowski, 1986, Franz, 1991, Baner, 1993, Piringer, 1992). Table 4-2 shows the test set of 13 different aroma compounds, with their properties and their structures. The experimental data were compared to estimations using different estimation methods of UNIFAC-FV, GCFLORY (1990), GCFLORY (1994) and ELBRO-FV. 

When a block copolymer is blended with a homopolymer that differs in composition from either block the usual result is a three-phase structure. Miscibility of the various components is not necessarily desirable. Thus styrene-butadiene-styrene block copolymers are recommended for blending with high density polyethylene to produce mixtures that combine the relative high melting behavior of the polyolefin with the good low temperature properties of the elastomeric midsections of the block polymers. 

Compare and contrast the structures and properties of low-density polyethylene, high-density polyethylene, and linear low-density polyethylene. 

Rigid Packaging PVDC is used in combination with skin layers (materials such as polypropylene, high-density polyethylene, and polystyrene) which provide the necessary structural properties to the package. 

The relationship between chemical structures and their physical performance is one of the central topics of polymer physics. lUPAC has recommended a whole set of names to describe the detailed chemical structures of polymer chains and their derivatives. However, in our daily communication, people prefer to use the popular names of polymers reflecting their characteristic physical performances, such as high-density polyethylene (HOPE), foamed polystyrene, thermoplastic elastomers, liquid crystal polymers, conductive polymers, and polyelectrolyte. Such terminology allows us to comprehend quickly the basic characteristics of chemical structures responsible for their specific physical properties. 

---