Solution terpolymerization processes of methyl methacrylate, dodecyl methacrylate, and octadecyl methacrylate
using bifunctional 1,1-di(tert-butylperoxy)-3,3,5-trimethylcyclohexane or monofunctional tert-butylperoxy-2-ethylhexanoate initiator were investigated. The first set of terpolymerizations was performed in 2 M xylene
solutions, isothermally at 91, 100, 105, and 115 °C. The terpolymerization kineticsconcentrations of molecular
species, kinetic chain length, molar mass averages as functions of the reaction timewas modeled by the
Villermaux−Blavier tendency kinetic model for radical polymerization. Complete monomer conversions and
high molar masses of terpolymers were achieved in a simple batch process with bifunctional initiator. The
second set of polymerization reactions was performed in 2 M mineral base oil solutions, under isothermal
conditions at 115 and 120 °C, using the bifunctional initiator. By varying the monomer mixture composition
and concentrations of the initiator and chain transfer agent, n-dodecyl mercaptan, the terpolymers of different
composition and molar mass were obtained. The solution properties of alkyl methacrylate terpolymers as
lubricating oil rheology modifierskinematic viscosity, viscosity index, shear stability, and pour pointwere
established. A strong correlation between molar mass distribution of synthesized polymers and rheological
properties of polymer solutions was revealed by an applied optimization procedure.