Summary: The chromatographic separation of ethylene‐propylene (EP) copolymers with regard to chemical composition was accomplished by a new technique ‐ high‐ temperature gradient HPLC. Using a mobile phase of ethylene glycol monobutylether (EGMBE) and 1,2,4–trichlorobenzene (TCB), and silica gel as the stationary phase, copolymers with different ethylene contents were separated according to their chemical compositions. Using a sample solvent of n‐decanol and a column temperature of 140 °C, chromatographic conditions were established that correspond to separation in a precipitation‐redissolution mechanism. With the aim to obtain further information on the separation process, the HPLC system was coupled to FTIR spectroscopy through a LC‐Transform interface. The FTIR data confirmed that the copolymers were separated according to the ethylene content of the eluted samples.
Ethylene - methyl methacrylate block copolymers are semicrystalline polymers that dissolve in organic solvents only at high temperatures. Accordingly, microstructure analysis by solution methods must be conducted at temperatures above 130°C. For the analysis of block copolymers of different compositions several analytical techniques were used, including high-temperature size-exclusion chromatography (SEC), hyphenated SEC-FTIR, and CRYSTAF (crystallisation analysis fractionation). While SEC with refractive index detection indicated a certain multimodality of the samples, SEC coupled with FTIR revealed that the samples were chemically inhomogeneous and may contain homo- and copolymer fractions. The presence of polyethylene and poly(methyl methacrylate) homopolymers in the copolymer samples was confirmed by CRYSTAF analysis, when the total concentration as well as the carbonyl group distribution were monitored separately. Chromatographic separation of the different sample components was achieved when liquid chromatography at critical conditions (LC-CC) was used. For the first time, true high-temperature LC-CC methods were developed operating at a column temperature of 140°C. As the stationary phase, silica gel was used. Suitable mobile phases were binary mixtures of 1,2,4-trichlorobenzene or 1,2- dichlorobenzene with cyclohexanone. Using LC-CC, the samples were separated into the copolymer and the homopolymer fractions.
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