Polymerization of Alkenes
- Page ID
- 3887
\( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)
\( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)
\( \newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\)
( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\)
\( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)
\( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\)
\( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)
\( \newcommand{\Span}{\mathrm{span}}\)
\( \newcommand{\id}{\mathrm{id}}\)
\( \newcommand{\Span}{\mathrm{span}}\)
\( \newcommand{\kernel}{\mathrm{null}\,}\)
\( \newcommand{\range}{\mathrm{range}\,}\)
\( \newcommand{\RealPart}{\mathrm{Re}}\)
\( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)
\( \newcommand{\Argument}{\mathrm{Arg}}\)
\( \newcommand{\norm}[1]{\| #1 \|}\)
\( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)
\( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\AA}{\unicode[.8,0]{x212B}}\)
\( \newcommand{\vectorA}[1]{\vec{#1}} % arrow\)
\( \newcommand{\vectorAt}[1]{\vec{\text{#1}}} % arrow\)
\( \newcommand{\vectorB}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)
\( \newcommand{\vectorC}[1]{\textbf{#1}} \)
\( \newcommand{\vectorD}[1]{\overrightarrow{#1}} \)
\( \newcommand{\vectorDt}[1]{\overrightarrow{\text{#1}}} \)
\( \newcommand{\vectE}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{\mathbf {#1}}}} \)
\( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)
\( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)
\(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)This page looks at the polymerisation of alkenes to produce polymers like poly(ethene) (usually known as polythene, and sometimes as polyethylene), poly(propene) (old name: polypropylene), PVC and PTFE. It also looks briefly at how the structure of the polymers affects their properties and uses.
Poly(ethene) (polythene or polyethylene)
Low density poly(ethene): LDPE
Manufacture
In common with everything else on this page, this is an example of addition polymerisation. An addition reaction is one in which two or more molecules join together to give a single product. During the polymerisation of ethene, thousands of ethene molecules join together to make poly(ethene) - commonly called polythene.
The number of molecules joining up is very variable, but is in the region of 2000 to 20000. Conditions:
| Temperature: | about 200°C |
| Pressure: | about 2000 atmospheres |
| Initiator: | a small amount of oxygen as an impurity |
Properties and uses
Low density poly(ethene) has quite a lot of branching along the hydrocarbon chains, and this prevents the chains from lying tidily close to each other. Those regions of the poly(ethene) where the chains lie close to each other and are regularly packed are said to be crystalline. Where the chains are a random jumble, it is said to be amorphous. Low density poly(ethene) has a significant proportion of amorphous regions.
One chain is held to its neighbours in the structure by van der Waals dispersion forces. Those attractions will be greater if the chains are close to each other. The amorphous regions where the chains are inefficiently packed lower the effectiveness of the van der Waals attractions and so lower the melting point and strength of the polymer. They also lower the density of the polymer (hence: "low density poly(ethene)").
Low density poly(ethene) is used for familiar things like plastic carrier bags and other similar low strength and flexible sheet materials.
High density poly(ethene): HDPE
Manufacture
This is made under quite different conditions from low density poly(ethene). Conditions:
| Temperature: | about 60°C |
| Pressure: | low - a few atmospheres |
| Catalyst: | Ziegler-Natta catalysts or other metal compounds |
Ziegler-Natta catalysts are mixtures of titanium compounds like titanium(III) chloride, TiCl3, or titanium(IV) chloride, TiCl4, and compounds of aluminium like aluminium triethyl, Al(C2H5)3. There are all sorts of other catalysts constantly being developed.
These catalysts work by totally different mechanisms from the high pressure process used to make low density poly(ethene). The chains grow in a much more controlled - much less random - way.
Properties and uses
High density poly(ethene) has very little branching along the hydrocarbon chains - the crystallinity is 95% or better. This better packing means that van der Waals attractions between the chains are greater and so the plastic is stronger and has a higher melting point. Its density is also higher because of the better packing and smaller amount of wasted space in the structure.
High density poly(ethene) is used to make things like plastic milk bottles and similar containers, washing up bowls, plastic pipes and so on. Look for the letters HDPE near the recycling symbol.
Poly(propene) (polypropylene): PP
Poly(propene) is manufactured using Ziegler-Natta and other modern catalysts. There are three variants on the structure of poly(propene) which you may need to know about, but we'll start from the beginning with a general structure which fits all of them.
The general structure
If your syllabus simply mentions the structure of poly(propene) with no more detail, this is adequate.
The trick is to think about the shape of the propene in the right way:
Now line lots of them up in a row and join them together. Notice that the double bonds are all replaced by single bonds in the process.
In a simple equation form, this is normally written as:
The three variations on this structure
You have got to remember that the diagrams above are 2-dimensional. Real poly(propene) chains are 3-dimensional. There are three different sorts of poly(propene) depending in how the CH3 groups are arranged in space. These are called isotactic, atactic and syndiotactic poly(propene). The commonly used version is isotactic poly(propene).
Isotactic poly(propene)
A bit of the isotactic poly(propene) chain looks like this:
This very regular arrangement of the CH3 groups makes it possible for the chains to pack close together and so maximise the amount of van der Waals bonding between them. That means that isotactic poly(propene) is quite strong either as a solid object or when it is drawn into fibres. This is the common form of poly(propene) which is used to make plastic crates and ropes amongst many other things. Look for the letters PP near the recycling symbol.
Atactic poly(propene)
In atactic poly(propene) the CH3 groups are orientated randomly along the chain.
This lack of regularity makes it impossible for the chains to lie closely together and so the van der Waals attractions between them are weaker. Atactic poly(propene) is much softer with a lower melting point. It is formed as a waste product during the manufacture of isotactic poly(propene) and its uses are limited. It is used, for example, in road paint, in making roofing materials like "roofing felt", and in some sealants and adhesives.
Syndiotactic poly(propene)
Syndiotactic poly(propene) is a relatively new material and is another regularly arranged version of poly(propene). In this case, every alternate CH3 group is orientated in the same way.
This regularity means that the chains can pack closely, and van der Waals attractions will be fairly strong. However, the attractions aren't as strong as in isotactic poly(propene). This makes syndiotactic poly(propene) softer and gives it a lower melting point.
Because syndiotactic poly(propene) is relatively new, at the time of writing uses were still being developed. It has uses in packaging - for example, in plastic film for shrink wrapping food. There are also medical uses - for example, in medical tubing and for medical bags and pouches. There are a wide range of other potential uses - either on its own, or in mixtures with isotactic poly(propene).
Poly(chloroethene) (polyvinyl chloride): PVC
Poly(chloroethene) is commonly known by the initials of its old name, PVC.
Structure
Poly(chloroethene) is made by polymerising chloroethene, CH2=CHCl. Working out its structure is no different from working out the structure of poly(propene) (see above). As long as you draw the chloroethene molecule in the right way, the structure is pretty obvious.
The equation is usually written:
It doesn't matter which carbon you attach the chlorine to in the original molecule. Just be consistent on both sides of the equation. The polymerisation process produces mainly atactic polymer molecules - with the chlorines orientated randomly along the chain. The structure is no different from atactic poly(propene) - just replace the CH3 groups by chlorine atoms.
Because of the way the chlorine atoms stick out from the chain at random, and because ot their large size, it is difficult for the chains to lie close together. Poly(chloroethene) is mainly amorphous with only small areas of crystallinity.
Properties and uses
You normally expect amorphous polymers to be more flexible than crystalline ones because the forces of attraction between the chains tend to be weaker. However, pure poly(chloroethene) tends to be rather hard and rigid.
This is because of the presence of additional dipole-dipole interactions due to the polarity of the carbon-chlorine bonds. Chlorine is more electronegative than carbon, and so attracts the electrons in the bond towards itself. That makes the chlorine atoms slightly negative and the carbons slightly positive. These permanent dipoles add to the attractions due to the temporary dipoles which produce the dispersion forces.
Plasticisers are added to the poly(chloroethene) to reduce the effectiveness of these attractions and make the plastic more flexible. The more plasticiser you add, the more flexible it becomes. Poly(chloroethene) is used to make a wide range of things including guttering, plastic windows, electrical cable insulation, sheet materials for flooring and other uses, footwear, clothing, and so on and so on.
Poly(tetrafluoroethene): PTFE
You may have come across this under the brand names of Teflon or Fluon.
Structure
Structurally, PTFE is just like poly(ethene) except that each hydrogen in the structure is replaced by a fluorine atom.
The PTFE chains tend to pack well and PTFE is fairly crystalline. Because of the fluorine atoms, the chains also contain more electrons (for an equal length) than a corresponding poly(ethene) chain. Taken together (the good packing and the extra electrons) that means that the van der Waals dispersion forces will be stronger than in even high density poly(ethene).
Properties and uses
PTFE has a relatively high melting point (due to the strength of the attractions between the chains) and is very resistant to chemical attack. The carbon chain is so wrapped up in fluorine atoms that nothing can get at it to react with it. This makes it useful in the chemical and food industries to coat vessels and make them resistant to almost everything which might otherwise corrode them.
Equally important is that PTFE has remarkable non-stick properties - which is the basis for its most familiar uses in non-stick kitchen and garden utensils. For the same reason, it can also be used in things like low-friction bearings.
Contributors
Jim Clark (Chemguide.co.uk)