SasolAnnual review and summarized financial information 2006
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Summary Creating an Industry Coal & Gasifiers Plant & Catalysts Economics & Chemicals Plastics & Synthol Reactors, Exploration & Gas-to-liguids  
 
 
•  Time line
Cellulose
•  Olefins
 
 
 
Callulose
 
Long chains    
 
pg42_1  
 
A graphic representation of an alpha olefin hexene molecule
 
 
Long chains
At about the same time a German scientist, Professor Hermann Standinger, proposed that molecules were held together not in blocks or networks, but formed long chains. That notion was further developed by a compatriot, Professor Herman Mark. Employed by IG Farbenindustrie as its director of research, he came to realise that major differences in polymers (many molecules joined together) would result from the degree to which their chains were branched (explanation coming up shortly). And different polymers would, of course, produce different thermoplastics.
 
We’ve seen that methane consists of one atom of carbon attached to four of hydrogen. Next comes ethane: two carbon atoms attached to each other, with each of their remaining hooks connected to a hydrogen atom - hence the chemical formula for ethane, C2H6. Now, if you use a high-temperature process to sever a hydrogen atom from each of the carbon atoms - it’s called dehydrogenation - you get ethylene (C2H4). To make use of the hooks that had connected them to those now-missing hydrogen atoms, the carbon atoms create a double-bond between themselves. The molecule, however, is called "unsaturated" because that double bond, as noted in an earlier chapter, is not a happy state of affairs; either of the carbon atoms would much rather connect with an atom in some other molecule. 
 
You can form long, merry chains in that way until some spoilsport hydrocarbon molecule comes along and effectively saturates the end of the chain 
 
Which, of course, they can quite easily if you put many ethylene molecules into a pot. The carbon atom in one ethylene molecule will remove one of its hooks from the other carbon atom in the same molecule and use it to bond with a carbon atom in another ethylene molecule. So you end up with a sort of Conga line of carbon atoms, each joined by its belt to the one in front, and holding out its arms sideways, with a hydrogen atom in each hand. 
 
You can form long, merry chains in that way until some spoilsport hydrocarbon molecule comes along and effectively saturates the end of the chain. During the course of its growth, the chain may have developed molecular branches. That happens when a hydrogen atom at some point along the chain serves to link it with a shorter, unsaturated chain of hydrocarbons drifting around in the neighbourhood. This can happen many times along the length of the main chain. 
 
But what has all that to do with plastics? 
 
 
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