The Lid’s Tale

Not long ago, we acquired a range of inexpensive storage vessels, ideal for keeping leftovers in the fridge before they go into yours truly, the family dustbin.  Here is an example: the steel dish is covered by a tight-fitting plastic (presumably polyethylene) lid.  Or it was tight-fitting when we bought it, but some of these lids are now so tight-fitting that they won’t even go on at all, and one or two have split in the attempt to force them on.  

Not long ago, we acquired a range of inexpensive storage vessels, ideal for

keeping leftovers in the fridge before they go into yours truly, the family

dustbin. 

Here is an example: the steel dish is covered by a tight-fitting

plastic (presumably polyethylene) lid.  Or it was tight-fitting when we bought

it, but some of these lids are now so tight-fitting that they won’t even go on

at all, and one or two have split in the attempt to force them

on.
 

 
First instinct might be to

blame the country of manufacture.  However, I think the problem lies in a lack

of detailed knowledge of polymer properties.  The manufacturer has probably

turned out a product that nicely matches specification, but is, like 99.99% of

the world’s population, not familiar with the science of how plastics perform

under ageing and wear & tear.
 
Plastics are a widely varied class of

materials — if you want to ask “how varied”, I would reply “describe a typical

mollusc”.  However, with polyethylene, we are dealing with a typical,

archetypical semicrystalline thermoplastic. The second word is easy: it

means one that you can melt and mould.  But the first word?
 
Some

plastics, like polystyrene, are not crystalline at all.  Heat them up, and you

get a sticky liquid, and as they cool, this sets into a hard glass.  But no

crystals have been formed — just like ordinary window glass, the liquid becomes

so stiff on cooling that it is effectively a solid.  It may look “crystal

clear”, but there is not the regular atomic or molecular order found in common

crystalline solids like table salt or granulated sugar.

Polyethylene,

above 140°C, is a sticky, gooey, clear liquid.  Cool it by some tens of degrees,

though, and it starts to crystallize.  The crystals start as tiny nuclei, and

begin to grow.  There are generally lots of these nuclei, maybe 1000 to a cubic

millimetre, and very soon the crystals have grown and are abutting on to each

other.  They do not completely fill up space, though.  Polyethylene molecules

are spaghetti like, and after a while in the remaining space the molecules are

so tangled up together they cannot sort themselves out any further.  So instead

of crystallizing into a hard solid, they form a rubbery sort of filler for the

crystals that have already grown.  That is why polyethylene can have some of the

stiffness of a solid and some of the flexibility of a

rubber.  (Picture: transmission electron micrograph showing crystals in matrix)

And now for the history of our

plastic lid.  It would have started out as a sack of pellets from the

polyethylene manufacturer, which would have been fed into some kind of hopper

and then into a melting oven.  Here is how the volume of polyethylene increases

as it is heated (data from Leo

Mandelkern of Florida State University[1]).

If it were a ‘simple’

solid, it would behave somewhat like the red curve.  From near room temperature

at A, it would expand slowly, until near the melting point at B, when it would

all turn into liquid with a much greater volume, and then continue expanding as

a liquid, rather more quickly than it did as a solid.

But not real

polyethylene (black curve).  The upward curvature at D shows that a proportion

of the solid is gradually turning into liquid all the way up the melting curve,

even though the final melt-out takes place over a range of a few degrees.  But

even ten or twenty degrees before this, the plastic would have become softer,

more bendy, and a bit sticky to the touch.

Now we have our molten

polyethylene, and we rapidly inject it into the mould and cool it very quickly. 

Speed is of the essence, in order to keep ‘cycle time’ down, out with one lid in

with the next in the same mould.

The next graph shows how the volume of 1

gram of polyethylene (PE) is made up of its rubbery (or ‘amorphous’) and

crystalline parts.  If we could cool it fast enough, in theory it would not

crystallize at all, and would form a glass.  In practice, this is very difficult

to achieve.  The only case I know of is where thin films of molten polyethylene

have been catapulted into slushy nitrogen at –210°C (mere liquid nitrogen would

not do: it would start to boil and an insulating film of bubbles would form on

the polyethylene so that it could not cool fast enough.)  Even if one could

achieve this with one’s bucket, it would crystallize as it warmed back up to

room temperature.  But if one could achieve such a state, one’s

gram of polyethylene would occupy nearly 1·2 cm3 of space

(A).

In our moulding process, though,

it crystallizes, not all the way to D, but to something like

B.  Our gram of PE now occupies about 1·06 cm3.  And

there it would sit, quite happily, part of a well-formed nicely fitting lid, if

only …

If only we did not do things like filling the container with hot

food, and washing it up in really hot water.  The lid was, as said before,

formed under very rapid cooling, and the plastic is far from being in anything

like an ‘equilibrium’ state.  Heat it up again, and the crystalline material

starts to melt slightly.  However, the non-crystalline part is now able to

crystallize more slowly, and into something more like an ‘equilibrium’ state. 

This means that the lid will transform into a more highly crystalline condition

such as C in the diagram.

This means that our lid had

shrunk, and it is more difficult to force it onto the steel dish.  Push too

hard, and the rim of the lid may — and sometimes does —

SNAP!

 
[1] Place to go if you’re

looking for a Tallahassee

Lassie?
 
 

Old NID
104505
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