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Mechanically Accelerated Depolymerization of Entangled Linear Polymer Melts
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DOI：10.1021/acs.macromol.5c00974.png)
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Abstract
En 中文
Mechanical forces can enhance the chemical depolymerization of synthetic polymers when shear flow accelerates chain scission. To quantify the extent of mechanically accelerated scission, the effect of simple shear flow (duration and strength) with low Weissenberg and Deborah numbers was investigated by considering the impact of applied work in both simple shear and shear dominated mixed flows. Hydrogenated polyisoprene was chosen as a model linear, entangled system. The conditions (strain amplitude, frequency, and shearing time) necessary to increase chain scission were assessed in the rubbery melt. Isothermal scission versus work curves were superposed by applying shift factors aT,S, whose Arrhenius-like temperature dependence provide an apparent energy barrier for chain scission of similar to 110 kJ/mol, which is likely a combination of the activation energy of viscosity and bond energy. These results provide a base for quantifying the impact of shear on depolymerization of polymer melts and highlight the connection between viscous dissipation and scission chemistry.
Keywords:
SCISSION DISTRIBUTION FUNCTION
FLOW-INDUCED SCISSION
CHAIN SCISSION
THERMAL-DEGRADATION
FLEXIBLE POLYMERS
MOLECULAR-WEIGHT
POLYPROPYLENE
POLYETHYLENE
EXTRUSION
DYNAMICS
Journal
IF:
5.2
Papers:
3.7W
Citations:
9.4W