Jump to content

Doze

Members
  • Posts

    3
  • Joined

  • Last visited

Everything posted by Doze

  1. Thank you very much for the help.
  2. Thank you very much for your reply, only if there was some kind of rewarding system here that I would be able to express my thanks better . There is another question that is getting to me, you don't have to answer it if you don't want to (you've helped me greatly enough anyway) How does HDPE become Isostatic or Syndiostatic through Ziegler-Natta catalytic polymerization OR anionic polymerization? All I know is the Electron transfer in initiation and that allows for the addition of monomers, however shouldn't the areas of attack be random like free radical polym. ? Thank you again.
  3. Hello Chemistry Community! I basically have to choose which polymer is better for water piping, though there is some chemistry I am not understanding associated with the relations of tacticity, crystallinity and strength of the polymers. (PVC and HDPE) I did some research, and found that PVC is atactic (or heterotactic) because of the Chlorine units on the backbone (yet it doesn't say why the chlorine makes it like that?). This makes PVC more amorphous making it harder to arrange into layers , making it less crystalline, unlike HPDE (which is very crystalline because it's non branched and syndiotactic).PVC is known for its strength and durability, apparently it's 'Semi-crystalline' and has much more compression strength than HDPE (9500 psi compared to 3500-3700 psi for HDPE). Is it for this reason ? : HDPE is far more crystalline, since it's linear and syndiotactic, though is it less stronger than PVC because of it only harnessing intermolecular forces within its chains, is this why? And PVC, which has covalent bonds (cross links?) between its chains because of its chlorine, which makes it stronger than HDPE regardless of how less crystalline it is? I doubt that is why though... I think it may be the molar mass distribution or something along the lines...maybe? 2) I also was wondering if the reason for HDPE's glass transition temperature being 120 to 130 °C (248 to 266 °F) compared to 80°C for PVC, was because HDPE is more crystalline? But aren't PVC's covalent bonds holding chains together? Because apparently glass transition allows 'molecular chains to slide past each other when a force is applied', shouldn't HDPE have a lower Tg temperature than PVC and have its molecules 'slide' easier when it reaches its Tg? This is really bugging me, I apologize for the rather lengthy question, though help would be much appreciated Thank you for your time.
×
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.