1994Journal of Applied Polymer ScienceRequires access

Structure and properties of maleated high‐density polyethylene

Yilong Wang, Deqiang Ji, Changlai Yang, Hongjin Zhang, Chuan Li Qin, Baotong Huang

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Abstract

Abstract Possible changes in the structure and properties of maleated polyethylene (HDPE–MA) at different degrees of grafting (D.G.) were examined. At the level of 1.6 maleic anhydride (MA)/100 ethylene units E, 70–80% of crystallinity of the parent PE was retained (DSC and WAXD). Both melting temperature and crystallization temperature decreased only slightly with increase in D. G. The lattice constantsaandbof the orthorhombic PE crystallites remained constant, althoughcwas constantly at a larger value. The presence of MA groups hampered the packing of PE chains, leading to an increase in PE crystallite sizes ofL̄110andL̄200with maleation. Of the viscoelastic relaxations, dynamic mechanical analysis showed easier segmental motions and thus lowering in γ‐, α‐ and β‐relaxation temperatures with maleation. The breaking strength (σb) increased slightly with maleation, whereas the elongation at break (εb) lowered due to interaction between the MA groups. In all, in HDPE‐MA up to a D. G. of 1.6 MA/100 E, PE properties were maintained to be used per se or as a compatibilizer for blends involving PE or in any other usage where retention of PE properties is desired. © 1994 John Wiley & Sons, Inc.

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Abstract Possible changes in the structure and properties of maleated polyethylene (HDPE–MA) at different degrees of grafting (D.G.) were examined. At the level of 1.6 maleic anhydride (MA)/100 ethylene units E, 70–80% of crystallinity of the parent PE was retained (DSC and WAXD). Both melting temperature and crystallization temperature decreased only slightly with increase in D. G. The lattice constantsaandbof the orthorhombic PE crystallites remained constant, althoughcwas constantly at a larger value. The presence of MA groups hampered the packing of PE chains, leading to an increase in PE crystallite sizes ofL̄110andL̄200with maleation. Of the viscoelastic relaxations, dynamic mechanical analysis showed easier segmental motions and thus lowering in γ‐, α‐ and β‐relaxation temperatures with maleation. The breaking strength (σb) increased slightly with maleation, whereas the elongation at break (εb) lowered due to interaction between the MA groups. In all, in HDPE‐MA up to a D. G. of 1.6 MA/100 E, PE properties were maintained to be used per se or as a compatibilizer for blends involving PE or in any other usage where retention of PE properties is desired. © 1994 John Wiley & Sons, Inc.

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Available abstract

Abstract Possible changes in the structure and properties of maleated polyethylene (HDPE–MA) at different degrees of grafting (D.G.) were examined. At the level of 1.6 maleic anhydride (MA)/100 ethylene units E, 70–80% of crystallinity of the parent PE was retained (DSC and WAXD). Both melting temperature and crystallization temperature decreased only slightly with increase in D. G. The lattice constantsaandbof the orthorhombic PE crystallites remained constant, althoughcwas constantly at a larger value. The presence of MA groups hampered the packing of PE chains, leading to an increase in PE crystallite sizes ofL̄110andL̄200with maleation. Of the viscoelastic relaxations, dynamic mechanical analysis showed easier segmental motions and thus lowering in γ‐, α‐ and β‐relaxation temperatures with maleation. The breaking strength (σb) increased slightly with maleation, whereas the elongation at break (εb) lowered due to interaction between the MA groups. In all, in HDPE‐MA up to a D. G. of 1.6 MA/100 E, PE properties were maintained to be used per se or as a compatibilizer for blends involving PE or in any other usage where retention of PE properties is desired. © 1994 John Wiley & Sons, Inc.

Key concepts: Crystallinity, High-density polyethylene, Maleic anhydride, Crystallite, Materials science, Polyethylene, Orthorhombic crystal system, Crystallization

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