TY - JOUR
T1 - Preparation of linear low-density polyethylene by the in situ copolymerization of ethylene with an iron oligomerization catalyst and rac-ethylene bis(indenyl) zirconium (IV) dichloride
AU - Zhang, Zhichenc
AU - Cui, Nannan
AU - Lu, Yingying
AU - Ke, Yucai
AU - Hu, Youliang
PY - 2005/3/1
Y1 - 2005/3/1
N2 - An iron oligomerization catalyst, [(2-ArN=C(Me))2C 5H3N]FeCl2 [Ar = 2,6-C6H 3(F)2], was combined with rac-ethylene bis(indenyl)zirconium (IV) dichloride [rac-Et(Ind)2ZrCl2] to prepare linear low-density polyethylene (LLDPE) by the in situ copolymerization of ethylene. A series of LLDPEs with different properties were prepared by the alteration of the reaction temperature, Fe/Zr molar ratio, Al(Fe + Zr) molar ratio, and reaction time. The structures of the polymers were characterized with differential scanning calorimetry, 13C NMR, gel permeation chromatography (GPC), and so forth. The melting points, crystallizations, and densities of the resulting products increased, and the average branching degree decreased, as the reaction temperature, Al/(Fe + Zr) ratio, and reaction time increased. The melting points, crystallizations, and densities of the polymers decreased, and the average branching degree increased, when the Fe/Zr ratio increased. The 13C NMR and GPC results showed that there were no unreacted α-olefins remaining in the resulting polymers because the percentage of low-molar-mass sections (C4-C 10) of the oligomers obtained with this catalyst was very high (>70%). In addition, the formation of polymers with two melting points under different reaction conditions was examined in detail, and the results indicated that the two melting points of the polymers could be attributed to polyethylene with different branches.
AB - An iron oligomerization catalyst, [(2-ArN=C(Me))2C 5H3N]FeCl2 [Ar = 2,6-C6H 3(F)2], was combined with rac-ethylene bis(indenyl)zirconium (IV) dichloride [rac-Et(Ind)2ZrCl2] to prepare linear low-density polyethylene (LLDPE) by the in situ copolymerization of ethylene. A series of LLDPEs with different properties were prepared by the alteration of the reaction temperature, Fe/Zr molar ratio, Al(Fe + Zr) molar ratio, and reaction time. The structures of the polymers were characterized with differential scanning calorimetry, 13C NMR, gel permeation chromatography (GPC), and so forth. The melting points, crystallizations, and densities of the resulting products increased, and the average branching degree decreased, as the reaction temperature, Al/(Fe + Zr) ratio, and reaction time increased. The melting points, crystallizations, and densities of the polymers decreased, and the average branching degree increased, when the Fe/Zr ratio increased. The 13C NMR and GPC results showed that there were no unreacted α-olefins remaining in the resulting polymers because the percentage of low-molar-mass sections (C4-C 10) of the oligomers obtained with this catalyst was very high (>70%). In addition, the formation of polymers with two melting points under different reaction conditions was examined in detail, and the results indicated that the two melting points of the polymers could be attributed to polyethylene with different branches.
KW - Branching degrees
KW - Copolymerization
KW - In situ copolymerization
KW - Linear low-density polyethylene
KW - Oligomers
KW - Polyethylene (PE)
KW - α-olefins
UR - https://www.scopus.com/pages/publications/14644429038
U2 - 10.1002/pola.20560
DO - 10.1002/pola.20560
M3 - 文章
AN - SCOPUS:14644429038
SN - 0887-624X
VL - 43
SP - 984
EP - 993
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
IS - 5
ER -