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Dissertations in Forestry and Natural Sciences

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Wood-plastic composites<br />

The properties of a polymer are primarily def<strong>in</strong>ed by its<br />

molecular structure. Homopolymers conta<strong>in</strong> only one type of<br />

monomer whereas copolymers or terpolymers consist of several<br />

k<strong>in</strong>ds of monomers. The branch<strong>in</strong>g of polymer cha<strong>in</strong>s has<br />

multiple effects on the polymer. For example, the highly<br />

branched low-density polyethylene (LDPE) is softer <strong>and</strong> has a<br />

lower density <strong>and</strong> poorer tensile strength than the more l<strong>in</strong>ear<br />

high-density polyethylene (HDPE). (Clemons et al. 2013)<br />

The properties of polymers also depend on its tacticity – the<br />

arrangement of monomers along the polymer backbone.<br />

Polymer tacticity can be divided <strong>in</strong>to three classes: an isotactic<br />

polymer has all of its substituents on the same side of the<br />

backbone, <strong>and</strong> polymers with alternat<strong>in</strong>g placements of<br />

substituents along the backbone are called syndiotactic. Atactic<br />

polymers lack any consistent arrangement <strong>in</strong> their substituents.<br />

(Clemons et al. 2013)<br />

The monomers of a copolymer can also be organized <strong>in</strong> a<br />

variety of ways (Clemons 2008). An alternat<strong>in</strong>g copolymer<br />

consists of two different monomers arranged <strong>in</strong> an alternat<strong>in</strong>g<br />

sequence with<strong>in</strong> the cha<strong>in</strong> of the molecule (ABABAB…). The<br />

organization of monomers <strong>in</strong> r<strong>and</strong>om copolymers is not def<strong>in</strong>ed<br />

(ABAABBBA…). Statistical copolymers have monomers<br />

arranged accord<strong>in</strong>g to a known statistical rule. Block<br />

copolymers are made up of polymerized monomer blocks. If a<br />

copolymer conta<strong>in</strong>s side cha<strong>in</strong>s that have a different<br />

composition compared with the ma<strong>in</strong> cha<strong>in</strong>, the polymer is<br />

termed as a graft copolymer.<br />

The crystall<strong>in</strong>ity of the polymer affects its thermal <strong>and</strong><br />

physical properties because the crystall<strong>in</strong>e regions <strong>in</strong>side the<br />

polymer structure <strong>in</strong>crease the <strong>in</strong>teractions between the<br />

polymer cha<strong>in</strong>s. When the structure of the polymer is highly<br />

ordered, there are fewer possibilities for the polymer cha<strong>in</strong>s to<br />

move relative to one another. Thus, more energy is required to<br />

transform the polymer <strong>in</strong>to an unordered fluid state, mean<strong>in</strong>g<br />

that polymers with high crystall<strong>in</strong>ity have higher melt<strong>in</strong>g po<strong>in</strong>ts<br />

<strong>in</strong> comparison with their more amorphous counterparts. (Beyler<br />

<strong>and</strong> Hirschler 2001) High crystall<strong>in</strong>ity also means that the<br />

<strong>Dissertations</strong> <strong>in</strong> <strong>Forestry</strong> <strong>and</strong> <strong>Natural</strong> <strong>Sciences</strong> No 222 29

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