Abstract
The influences of short chain branching (SCB) and molecular (Mw) weight of low density polyethylene (LDPE) on the solid state properties of polypropylene (PP)-LDPE blends were investigated by mechanical and thermal techniques. DSC analysis of all blends exhibit a double melting peak at all compositions studied thus suggesting that both PP and LDPE crystals exist separately in the solid state. It was found that the SCB and Mw of LDPE influenced the modulus and ultimate tensile strength of the blends. However, elongation at break seems to be independent of the molecular characteristics of the pure homopolymer especially at PP blend composition greater than 50%. LDPE with high SCB showed broader melting peaks. Addition of a small amount of a low Mw LDPE (10%) resulted in a higher elongation at break than a high Mw LDPE. There is likely a correlation between the presence of a new peak in the thermograms of PP-rich blends and the observed poor elongation at break.
| Original language | English |
|---|---|
| Pages (from-to) | 130-137 |
| Number of pages | 8 |
| Journal | Macromolecular Symposia |
| Volume | 263 |
| Issue number | 1 |
| DOIs | |
| State | Published - Feb 2008 |
Keywords
- Blends
- Low density polyethylene
- Molecular weight
- Polypropylene
- Short chain branching
ASJC Scopus subject areas
- Condensed Matter Physics
- Organic Chemistry
- Polymers and Plastics
- Materials Chemistry
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