girlworld_club
Member
i can't seem to find the answers in any textbook.
Yea its the same, but to replace a hydrogen with chlorine atom and benzene ring involves extra process of a substitution reaction, before u start the polymerisation.Pretty sure its same as polyethylene but just replace the hydrogen with the chlorine atom and benzene ring respectively.
So initiation, propagation, termination.
Yep yep, but I think you can start off with the actual monomer as being Styrene/Vinyl ChlorideYea its the same, but to replace a hydrogen with chlorine atom and benzene ring involves extra process of a substitution reaction, before u start the polymerisation.
Yep cos Peroxide radical's used because it has an unpaired electron I think which makes it more reactivedoes it use the same radical?
benzoyl peroxide is the common one innit? It has easy to break O-O bond for reactive radicalsYep cos Peroxide radical's used because it has an unpaired electron I think which makes it more reactive
Yeah you use it for that reason and then you split the peroxide molecule up into 2 peroxide radicals - each reacts with separate monomers and they propagate and eventually collide with each other in the termination reaction and form the polymer AFAIK.benzoyl peroxide is the common one innit? It has easy to break O-O bond for reactive radicals
Yes, and then the initiator molecule is engulfed by the reaction and so is no longer present at termination!Yeah you use it for that reason and then you split the peroxide molecule up into 2 peroxide radicals - each reacts with separate monomers and they propagate and eventually collide with each other in the termination reaction and form the polymer AFAIK.
Hahaha (Y)Yes, and then the initiator molecule is engulfed by the reaction and so is no longer present at termination!
We are a good team! finishing each others sentences! lol
It's an 'application' of your knowledge of LDPE production apparently...why do we even need to know this?