In situ polymerization of ethylene with functionalized multiwalled carbon nanotubes using a zirconocene aluminohydride system in solution

This study reports nanocomposite synthesis based on high‐density polyethylene with carbon nanotubes through in situ polymerization by coordination, and the use of an aluminohydride zirconocene/MAO system as a catalyst. Nanocomposites of linear polyethylene exhibit higher molar masses than pure high‐density polyethylene synthesized under similar conditions; where multiwalled carbon nanotubes (MWCNTs) acted as nucleating agents, shifting the crystallization temperature to higher values than neat high‐density polyethylene. Well‐dispersed MWCNTs in the HDPE matrices of the obtained nanocomposites are observed by SEM, where most of the nanocomposites showed an improvement in their thermal stability and electric conductivity, besides it is possible to obtain nanocomposites containing up to 41 wt% of nanofiller in the polymeric matrix. The aluminohydride complex n‐BuCp2ZrH3AlH2, activated with MAO at Al/Zr ratios of 2000, produced homogeneous HDPE/MWCNT composites under in situ polymerization conditions, at 70°C and 2.9 bar of ethylene pressure, with minimal residual alumina in the HDPE matrix. HDPE and MWCNT composites. Polyethylene with conductive properties. HDPE with higher thermal resistance.