Modelling elongational viscosity overshoot and brittle fracture of low-density polyethylene melts

被引:16
作者
Wagner, Manfred H. [1 ]
Narimissa, Esmaeil [2 ,3 ]
Poh, Leslie [2 ,3 ]
Huang, Qian [4 ]
机构
[1] Berlin Inst Technol TU Berlin, Polymer Engn Polymer Phys, Ernst Reuter Pl 1, D-10587 Berlin, Germany
[2] Technion Israel Inst Technol IIT, Dept Chem Engn, IL-32000 Haifa, Israel
[3] Guangdong Technion Israel Inst Technol GTIIT, Dept Chem Engn, Shantou 515063, Peoples R China
[4] Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
关键词
Low-density polyethylene; HMMSF model; Elongational viscosity; Viscosity overshoot; Branch point withdrawal; Brittle fracture; BRANCHED POLYMER MELTS; STRESS FUNCTION MODEL; MULTIMODE MSF MODEL; CONSTITUTIVE-EQUATIONS; EXTENSIONAL VISCOSITY; CHAIN STRETCH; STEADY-STATE; FLOW; RHEOLOGY; PREDICTION;
D O I
10.1007/s00397-022-01328-1
中图分类号
O3 [力学];
学科分类号
08 ; 0801 ;
摘要
The Hierarchical Multi-mode Molecular Stress Function (HMMSF) model predicts the elongational and multiaxial extensional viscosities of polydisperse linear polymer melts based exclusively on their linear viscoelastic characterization and a single nonlinear material parameter, the so-called dilution modulus G(D). For long-chain branched (LCB) polymer melts such as low-density polyethylene (LDPE), the HMMSF model describes quantitatively the elongational stress growth coefficient up to the maximum of the elongational viscosity but fails to predict the existence of the maximum and the following steady-state viscosity. By taking into account branch point withdrawal in elongational flow of LCB melts, we extend the HMMSF model and show that the maximum of the elongational viscosity can be characterized by a single additional parameter, the characteristic stretch (lambda) over bar (m), while the steady-state tensile stress and the elongational viscosity depend only on the dilution modulus G(D) as in the case of linear polydisperse melts. Comparison of predictions of the Extended Hierarchical Multi-mode Molecular Stress Function (EHMMSF) model to experimental data of 5 LDPE melts with widely different molecular weights, polydispersities and densities, and a model polystyrene pom-pom polymer shows good agreement within experimental accuracy in constant elongational-rate flow as well as stress relaxation after steady and reversed elongational flow. For the LCB melts considered, we report differences in the specific Hencky strain at the maximum of the tensile stress as quantified by the characteristic stretch (lambda) over tilde (m), and we discuss correlations between polydispersity, dilution modulus G(D), and strain hardening potential of the LDPE melts. We also extend the fracture criterion for brittle fracture of monodisperse polymer melts to the case of polydisperse polymers and find reasonable agreement with experimental evidence.
引用
收藏
页码:281 / 298
页数:18
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