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Polymerization of ethylene to polyethylene is described by the following chemical equation: n CH 2 =CH 2 (gas) → [−CH 2 −CH 2 −] n (solid) ΔH/n = −25.71 ± 0.59 kcal/mol (−107.6 ± 2.5 kJ/mol) [23] Ethylene is a stable molecule that polymerizes only upon contact with catalysts. The conversion is highly exothermic.
HDPE is known for its high strength-to-density ratio. [4] The density of HDPE ranges from 930 to 970 kg/m 3. [5] Although the density of HDPE is only marginally higher than that of low-density polyethylene, HDPE has little branching, giving it stronger intermolecular forces and tensile strength (38 MPa versus 21 MPa) than LDPE. [6]
Low-density polyethylene (LDPE) is a thermoplastic made from the monomer ethylene. It was the first grade of polyethylene, produced in 1933 by John C. Swallow and M.W Perrin who were working for Imperial Chemical Industries (ICI) using a high pressure process via free radical polymerization. [1] Its manufacture employs the same method today.
Epoxide monomers may be cross linked with themselves, or with the addition of a co-reactant, to form epoxy; BPA is the monomer precursor for polycarbonate; Terephthalic acid is a comonomer that, with ethylene glycol, forms polyethylene terephthalate. Dimethylsilicon dichloride is a monomer that, upon hydrolysis, gives polydimethylsiloxane.
The degradation of polyethylene occurs by random scission—a random breakage of the bonds that hold the atoms of the polymer together. When heated above 450 °C, polyethylene degrades to form a mixture of hydrocarbons. In the case of chain-end scission, monomers are released and this process is referred to as unzipping or depolymerization ...
The name of each polyolefin indicates the olefin from which it is prepared; for example, polyethylene is derived from ethylene, and polymethylpentene is derived from 4-methyl-1-pentene. Polyolefins are not olefins themselves because the double bond of each olefin monomer is opened in order to form the polymer.
To clarify, the polymer is named using the polymer class name followed by a colon and the name of the monomer, i.e., class name:monomer name. Thus on the left and right, respectively, are polyalkylene:vinyloxirane and polyether:vinyloxirane.
Typical monomers are nonpolar ethene and propene. The development of coordination polymerization that enables copolymerization with polar monomers is more recent. [4] Examples of monomers that can be incorporated are methyl vinyl ketones, [5] methyl acrylate, [6] and acrylonitrile. [7] Illustrative metallocene-based coordination catalysts