Absolute molar mass determination in mixed solvents. 1. Solving for the SEC/MALS/DRI "trivial" case.

Size-exclusion chromatography (SEC) with on-line static light scattering, specifically multi-angle static light scattering (MALS), and differential refractometry (DRI) detection remains the premier method by which to determine absolute, calibrant-independent molar masses of polymers. The method is restricted to the use of either neat solvents or solvents with a small amount of additive. In mixed solvents, preferential solvation (i.e., the enrichment, within the solvated volume of the polymer in solution, of one solvent over the other as compared to the solvent ratio outside said volume) leads to errors in the areas of the MALS and DRI chromatograms, as the solvent baseline does not accurately represent the solvent contribution to these detectors' peaks. A seemingly trivial way by which to overcome this problem is through the use of an isorefractive solvent pair. This "trivial" solution is complicated by the fact that the solvents in the pair must be miscible with each other in all proportions; the individual solvents as well as the mix must be able to fully dissolve the analyte; the solvents must possess sufficient optical contrast with the solution so as to generate an adequate detector signal; the solvent mix must be compatible with the chromatographic stationary phase, such that enthalpic contributions to the separation are minimal and analyte recovery from the columns is quantitative; and the difference in the Rayleigh factors of the solvents can be ignored. Herein, we present the analysis of narrow dispersity polystyrene (PS) and poly(methyl methacrylate) (PMMA) samples, across a four-fold range in molar mass, using SEC/MALS/DRI in a mix of tetrahydrofuran (THF) and methyl isoamyl ketone (MIAK), solvents which are shown to be isorefractive with each other at the temperature and wavelength of the experiments. Molar mass averages and dispersities are demonstrated to be statistically independent of solvent composition and to correspond well to the values in neat THF. The experiments were augmented by the use of on- and off-line quasi-elastic light scattering and of off-line MALS and DRI, to study the effect of solvent composition on polymer size in solution and on dilute solution thermodynamics. Additionally, 1H nuclear magnetic resonance spectroscopy was used to study the effect of tacticity on the insolubility of PMMA100 in 100% MIAK. We believe this constitutes the first example of obtaining accurate molar masses of polymers by SEC/MALS/DRI employing mixed solvents. The value of these experiments to other forms of macromolecular liquid chromatographic separations is also noted.

Onflow liquid chromatography at critical conditions coupled to (1)H and (2)H nuclear magnetic resonance as powerful tools for the separation of poly(methylmethacrylate) according to isotopic composition.

The present work addresses a major challenge in polymer chromatography by developing a method to separate and analyze polymers with identical molar masses, chemical structures and tacticities that is solely based on differences in isotope composition. For the first time, liquid chromatography at critical conditions (LCCC) was used to separate PMMA regarding the H and D isotopes. At critical conditions of H-PMMA, D-PMMA eluted in the adsorption mode and vice versa. By online onflow LCCC-NMR, both PMMA species were clearly identified. Different from other detectors, NMR can distinguish between H and D. Onflow LCCC-H/NMR and LCCC-D/NMR measurements were carried out and the H/D-blend components were detected. (1)H and (13)C NMR provided the tacticity of protonated PMMA. Double resonance (13)C{H} and triple resonance (13)C{H,D} provided the tacticity of the deuterated samples. Samples with similar tacticities were used to ensure that separation occurs solely regarding the isotope labeling.

Asymmetrical flow field-flow fractionation as a novel technique for the analysis of PS-b-PI copolymers.

Asymmetrical flow field-flow fractionation (AF4) was used as a fractionation technique to investigate the molecular heterogeneity of poly(styrene-b-isoprene) diblock copolymers synthesized by either sequential living anionic polymerization or coupling of living precursor blocks. AF4 coupled to multi-angle laser light scattering (MALLS), refractive index (RI), and ultraviolet (UV) detectors was used to separate the diblock copolymers from the homopolymers and coupling products, and the molar masses of the different components were analyzed. In order to get more information about the separated block copolymers, homopolymers, and coupling products, fractions were collected directly after the AF4 channel. The collected fractions were analyzed offline by (1)H NMR to provide identification of the different species and additional information on the true chemical composition, and the microstructure of the diblock copolymer was obtained.

Comprehensive two-dimensional liquid chromatography for the separation of protonated and deuterated polystyrene.

Liquid chromatography at critical conditions (LCCC) has been shown to be a powerful method for the separation of complex polymers regarding chemical composition, functionality, or molecular topology. LCCC has never been used, however, to separate polymers according to the degree of deuteration. This is a very challenging task since polymers shall be separated that are identical regarding molar mass, endgroups and chemical composition. In the present work, critical conditions were established in such a way that one component of a complex mixture elutes at critical conditions, whereas the other component shows size exclusion chromatography (SEC) behaviour. Blends of protonated (h) and deuterated (d) polystyrene (PS) were separated by LCCC at critical conditions of both h-PS and d-PS. Depending on the molar masses of the blend components, baseline separation could be achieved. In order to improve the separation further, comprehensive two-dimensional liquid chromatography was carried out on a number of model blends. In the first dimension LCCC was used, which separated the blends according to isotopic effects whereas in the second dimension the separation took place with respect to hydrodynamic volume. In order to further improve the separation of a number of blends a separation protocol was used where one component shows SEC conditions whereas the other component shows liquid adsorption chromatography (LAC) conditions. This separation protocol was achieved by varying the column temperature.

Analysis of polystyrene-b-polyisoprene copolymers by coupling of liquid chromatography at critical conditions to NMR at critical conditions of polystyrene and polyisoprene.

For the investigation of the molecular heterogeneity of polystyrene-b-polyisoprene block copolymers, a chromatographic separation method, namely liquid chromatography at critical conditions was developed. This method was coupled on-line with (1)H-NMR(where NMR stands for nuclear magnetic resonance) for the comprehensive analysis of the polystyrene-b-polyisoprene copolymers. The copolymers were synthesized by two different methods: sequential living anionic polymerization and coupling of living precursor blocks. While (1)H-NMR allows just for the analysis of the bulk chemical composition of the block copolymers, the coupling with liquid chromatography at critical conditions provides selective molar mass information on the polystyrene and polyisoprene blocks within the copolymers. The polyisoprene block molar mass is determined by operating at chromatographic conditions corresponding to the critical point of adsorption of polystyrene and size exclusion chromatography mode for polyisoprene. The molar mass of the polystyrene block is determined by operating at the critical conditions of polyisoprene. In addition to the molar mass of each block of the copolymers, the chemical composition distribution of the block copolymers was determined. By using the coupling of liquid chromatography at critical conditions to (1)H-NMR, one can also detect the homopolymers formed during synthesis. Finally the microstructure of the polyisoprene block in the copolymers was evaluated as a function of molar mass.

Characterisation of blends of polyisoprene and polystyrene by on-line hyphenation of HPLC and (1) H-NMR: LC-CC-NMR at critical conditions of both homopolymers.

Blends of polystyrene (PS) and polyisoprene (PI) were analysed by on-line hyphenation of LC at critical conditions and (1) H-NMR. Chromatography at critical conditions was established for both PS and PI. At both critical conditions, a perfect separation into the blend components was achieved. By operating at critical conditions of one blend component and size exclusion mode for the other it is possible to determine the molar mass using a suitable calibration. By using NMR as a detector, the microstructure of PI can be identified, quantified and the chemical composition of the blends can be calculated by monitoring the signal intensities of the olefinic protons of isoprene and the aromatic protons of PS.

Two-dimensional chromatography of complex polymers, 8. Separation of fatty alcohol ethoxylates simultaneously by end group and chain length.

A comprehensive two-dimensional liquid chromatography system was developed to precisely describe the molecular heterogeneity of fatty alcohol ethoxylates. The end-group functionality was analyzed by gradient HPLC while ethylene oxide oligomer distributions were characterized by liquid adsorption chromatography. A baseline separation of all functionality fractions irrespective of the ethylene oxide oligomer chain length was achieved on nonpolar X-Terra(®) C(18) with a methanol-water gradient, whereas an isocratic flow of isopropanol-water on a polar Chromolith(®) Si column gave a separation according to the oligomer chain length without interference of the end-group distribution. The combination of these two methods to conduct online two-dimensional liquid chromatography experiments resulted in a comprehensive two-dimensional picture on the molecular heterogeneity of the sample.

Two-dimensional chromatography of complex polymers, 8. Separation of fatty alcohol ethoxylates simultaneously by end group and chain length.

A comprehensive two-dimensional liquid chromatography system was developed to precisely describe the molecular heterogeneity of fatty alcohol ethoxylates. The end-group functionality was analyzed by gradient HPLC while ethylene oxide oligomer distributions were characterized by liquid adsorption chromatography. A baseline separation of all functionality fractions irrespective of the ethylene oxide oligomer chain length was achieved on nonpolar X-Terra C(18) with a methanol-water gradient, whereas an isocratic flow of isopropanol-water on a polar Chromolith Si column gave a separation according to the oligomer chain length without interference of the end-group distribution. The combination of these two methods to conduct online two-dimensional liquid chromatography experiments resulted in a comprehensive two-dimensional picture on the molecular heterogeneity of the sample.