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.
Copolymers of ethylene with 1-decene, 1-tetradecene and 1-octadecene were prepared using the catalyst system racEt[Ind]2ZrCl2/MAO and were analysed with regard to chemical heterogeneity using crystallisation analysis fractionation (CRYSTAF), differential scanning calorimetry (DSC) and size exclusion chromatography coupled to FTIR (SEC-FTIR). The melting and crystallisation temperatures from DSC decrease linearly with increasing amount of comonomer, independently of the nature thereof. The decrease in crystallisation temperature from CRYSTAF of copolymers with higher 1-olefin content indicates a small dependence on the length of the side chain. The chemical heterogeneity of the copolymers as analysed by DSC and CRYSTAF broadens with increasing comonomer concentration.
ABSTRACT:The growing number of heterogeneous polymeric species that are being synthesized places increasing demands on existing analytical techniques. Although sizeexclusion chromatography (SEC) has established itself as a powerful analytical tool, it has its limits when complex polymers, e.g., graft copolymers, must be analyzed. In this case, complementary techniques such as gradient HPLC and liquid chromatography at critical conditions (LCCC) are more favorable. The present study describes the synthesis and analysis of methyl methacrylate-and styrene-grafted epoxidized natural rubber by different chromatographic techniques. The grafting efficiency was evaluated by gradient HPLC under normal and reversed phase conditions. Methyl methacrylate-grafted ENR50 was further analyzed by LCCC, where separation of the rubber and grafted rubber occurred according to chemical composition but was independent of the molar mass of the methyl methacrylate homopolymers. This was followed by the combination of LCCC and SEC, where separation was achieved in two dimensions. Relevant deductions were made of both the chemical composition distribution and the molar mass distribution of the functional groups of methyl methacrylategrafted ENR50.
ABSTRACT:The evaluation of heterogeneous polymeric species by a selective, dual detector size-exclusion chromatography setup can provide accurate results on the incorporation of specific functional groups in copolymers as a function of the molar mass distribution. However, when non-UV-absorbing species are used in copolymerization reactions, the dual detector method becomes less reliable. By interfacing a Fourier transform infrared (FTIR) spectrometer with size-exclusion chromatography (SEC), the problem can be overcome, making it possible to map non-UV-absorbing species as a function of the molar mass distribution. Coupling takes place via a solvent-evaporation stage, which delivers the mobile phase as a dry, solvent-free polymeric film onto a germanium disk. In this article, styrene and methyl methacrylate were grafted onto epoxidized natural rubber (ENR50) and analyzed by SEC. The accuracy of FTIR as a suitable detector was evaluated by comparing results from a dual detector SEC setup and FTIR coupled to SEC. FTIR proved to be a successful detector for the analysis of non-UV-absorbing species. This was consequently followed by the characterization of methyl methacrylategrafted ENR50. From the relevant data, Gram-Schmidt and contour plots could be made to indicate the incorporation of methyl methacrylate into the grafted epoxidized natural rubber as a function of the molar mass distribution.
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