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Updated: Jan 13, 2026

Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
Published on: November 27, 2015
High-Pressure Phase Behavior of α-Olefin + n-Hexane + Ethylene/1-Octene Copolymer Systems: Experimental Study and
Ruijun Zhang1, Ziyi Dong2, Qiqi He1
1College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao 266555, China.
Abstract:
Accurate knowledge of phase behavior in polyolefin-solvent mixtures is critical for ensuring stable operation and safe scale-up of industrial solution polymerization processes. The binary (n-hexane + ethylene/1-octene copolymer, POE96k-10) and ternary (α-olefin + n-hexane + POE96k-10) phase behaviors were investigated via a visual high-pressure cell (POE96k-10: Mw = 96 kg·mol-1, Mw/Mn = 3.87, 1-octene mole fraction = 10.31 mol%) at temperatures of 380~480 K and pressures as high as 14 MPa. To systematically analyze the effects of α-olefin mass fraction and type on phase transition, four industrially relevant α-olefins (ethylene, 1-butene, 1-hexene, and 1-octene) were investigated. The results show that the phase transition temperature and pressure for liquid-liquid and liquid-vapor transitions show an approximately linear dependence on α-olefin mass fraction. Ethylene, 1-butene, and 1-hexene lower the phase transition temperature, whereas 1-octene increases it. Ethylene exhibits a strong anti-solvent effect, significantly lowering the transition temperature while increasing the phase transition pressure. The modified Sanchez-Lacombe equation of state (MSL EOS) effectively correlates and reproduces the phase equilibrium data of the α-olefin + n-hexane + POE96k-10 ternary systems, though its accuracy decreases with increasing α-olefin chain length.
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