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The molecular weight development with N-vinylformamide conversions was measured using a gel permeation chromatography (GPC).
The effects on the molecular weight development of chain segregation in emulsion polymerization are discussed both theoretically and experimentally.
The model is capable of predicting the conversion, composition and molecular weight development up to limiting conversions.
A kinetic model based on free volume theory was proposed to describe the polymerization kinetics and molecular weight development.
The effect of stabilizer concentration and controller structure and concentration on polymerization rate and molecular weight development was analyzed.
A molecular species model is used to calculate the molecular weight moments of the optimized prepolymer and to calculate the molecular weight development in a solid-state polymerization.
Similar(54)
General analytical expressions for the number- and weight-average molecular weight developments are obtained.
A comprehensive kinetic model for ethylene copolymerization in the presence of a multisite Ziegler Natta catalyst is considered to describe the molecular weight developments in the FBR.
To represent the kinetics of ethylene polymerization a general reaction mechanism is considered and the method of moments is employed to calculate the molecular weight developments.
Thus, the HuCAL® principle enables the rapid and high-throughput development of human antibodies by optimisation strategies proven useful in classical low molecular weight drug development.
The effect of such compartmentalization of the reaction system on the molecular weight distribution development in non-linear polymerization is investigated by application of newly developed simulation models for emulsion polymerizations that include chain transfer to polymer and terminal double bond polymerization.
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