High-temperature HPLC Research Articles

Хроматографические методы определения биохимических показателей свинины

The study of the qualitative composition of the muscle tissue of animals is necessary in connection with the influence of the nutrient content on the technological, taste and dietary properties of meat. The major known changes in the biochemical parameters of the animal tissues are in the content of amino acids and fatty acids, etc. The aim of the work was to compare different chromatographic methods and to identify the most effective of them for the determination of fatty acids and amino acids in pig meat. The following HPLC methods are known for analyzing food products: ultra-HPLC, «hydrophilic» chromatography, two-dimensional and multidimensional HPLC methods, chiral chromatography, express chromatography, capillary HPLC, nano-HPLC, micellar HPLC, HPLC on monolithic columns, HPLC on surface porous sorbents, immunochromatographic methods, green chromatography, high-temperature HPLC. The most common methods for the determination of amino acids and fatty acids are reversed-phase and cation-exchange HPLC.

The elution behavior of cyclosporine congeners in a developed HPLC system reflects the lipophilicity

Recently, the development of cyclic peptide drugs has accelerated. To develop an analytical method to determine the physicochemical properties of these lipophilic drug candidates, we investigated the separation mechanism of cyclosporine congeners A, B, C, and D using HPLC with a column packed with 2-μm nonporous octadecylsilyl silica particles at high temperature. The four congeners were eluted with good repeatability in terms of retention time, peak area, and theoretical plate number. A difference of one amino acid in the eleven amino-acid sequence of the cyclosporine congeners was able to be recognized by our system within 4 min by isocratic elution, and the resolution was greater than 1.68. The calculated logP values of these congeners were well correlated with the retention factors with a correlation coefficient of 0.991. We could elucidate the separation mechanism of cyclosporine congeners on the high-temperature HPLC system. These results show that this method using HPLC on a column packed with 2-μm nonporous octadecylsilyl silica particles can be used for studying the lipophilicity of cyclosporine congeners.

Multidimensional chromatographic analysis of carboxylic acid-functionalized polyethylene

Carboxy-functionalized polyethylene is comprehensively analysed using a multidimensional fractionation approach based on high-temperature HPLC, two-dimensional liquid chromatography and selective infrared detection.

Combination of TREF, high-temperature HPLC, FTIR and HPer DSC for the comprehensive analysis of complex polypropylene copolymers

A novel, powerful analytical technique, preparative temperature rising elution fractionation (prep TREF)/high-temperature (HT)-HPLC/Fourier transform infrared spectroscopy (FTIR)/high-performance differential scanning calorimetry (HPer DSC)), has been introduced to study the correlation between the polymer chain microstructure and the thermal behaviour of various components in a complex impact polypropylene copolymer (IPC). For the comprehensive analysis of this complex material, in a first step, prep TREF is used to produce less complex but still heterogeneous fractions. These chemically heterogeneous fractions are completely separated by using a highly selective chromatographic separation method--high-temperature solvent gradient HPLC. The detailed structural and thermal analysis of the HPLC fractions was conducted by offline coupling of HT-HPLC with FTIR spectroscopy and a novel DSC method--HPer DSC. Three chemically different components were identified in the mid-elution temperature TREF fractions. For the first component, identified as isotactic polypropylene homopolymer by FTIR, the macromolecular chain length is found to be an important factor affecting the melting and crystallisation behaviour. The second component relates to ethylene-propylene copolymer molecules with varying ethylene monomer distributions and propylene tacticity distributions. For the polyethylene component (last eluting component in all semi-crystalline TREF fractions), it was found that branching produced defects in the long crystallisable ethylene sequences that affected the thermal properties. The different species exhibit distinctively different melting and crystallisation behaviour, as documented by HPer DSC. Using this novel approach of hyphenated techniques, the chain structure and melting and crystallisation behaviour of different components in a complex copolymer were investigated systematically.

Comprehensive high temperature two-dimensional liquid chromatography combined with high temperature gradient chromatography-infrared spectroscopy for the analysis of impact polypropylene copolymers

Impact polypropylene copolymers (IPC) are extremely complex materials that can only be effectively analysed by multidimensional analytical approaches. IPC consists of isotactic polypropylene (iPP) as the major phase, ethylene–propylene (EP) copolymers of various compositions and small amounts of polyethylene. The molecular heterogeneity of two IPC samples having different ethylene contents was studied by using a novel cross-fractionation technique, developed from a combination of various analytical separation methods into an effective characterisation tool for complex polyolefins. The initial step involves the fractionation of the sample into EP rubber, EP segmented copolymer, and iPP, by preparative temperature rising elution fractionation (TREF). The resulting fractions are still distributed with regards to chemical composition and molar mass. The separation with respect to these parameters is conducted by comprehensive HT 2D-LC. This is the first time that the individual components in all TREF fractions of an IPC are separated and analysed mutidimensionally, by both SEC-FTIR, high-temperature (HT) HPLC-FTIR, and HT 2D-LC. Molar mass analysis of the chemically homogeneous fractions from HT HPLC is accomplished by HT SEC in the second dimension of HT 2D-LC. The chemical composition of all species is determined by coupling FTIR spectroscopy to HT HPLC via an LC-transform interface. This novel approach reveals the capability of this hyphenated technique to determine the exact chemical composition of the individual components in the complex TREF fractions of IPCs. The HT HPLC-FTIR results confirm the separation mechanism in the given chromatographic system using a 1-decanol to TCB solvent gradient and a Hypercarb stationary phase. The components of differing chemical composition are separated according to the nature and length of the propylene/ethylene segments, with their arrangement in the chains strongly affecting their adsorption/desorption on the stationary phase. FTIR analysis provides information on the ethylene and propylene contents of the fractions as well as on the ethylene and propylene crystallinities.

Random and block copolymers based on 4-methyl-1-pentene and 1-pentene

The zirconium acetamidinate catalyst {Cp*Zr(Me)2[N(Et)C(Me)N(tBu)]} (Cp* = ŋ5-C5Me5) was used to synthesize both random and block copolymers based on 4-methyl-1-pentene (4M1P) and 1-pentene. The polymers have been characterized by NMR spectroscopy, SEC, DSC, high temperature HPLC and CRYSTAF. Unexpectedly, the yields and molecular weights decreased with increasing amounts of 1-pentene. The reason for this behavior is that 1-pentene occasionally undergoes 2,1-misinsertions trapping the catalyst in a dormant state. These 2,1-misinsertions do not seem to occur with the bulky 4M1P (branched α-olefin). Adding a small amount of ethylene reactivates the catalyst. Unlike most semi-crystalline polymers, the density of the crystalline phase of isotactic P4M1P can be lower than of the amorphous phase, when crystallized under very high pressures. To characterize this peculiar behavior of 4M1P-based polymers, various samples have been subjected to Pressure-Volume-Temperature (PVT) measurements. While the P4M1P homopolymers and block copolymers show the expected decrease in specific volume upon crystallization, the 4M1P-rich random copolymers proved not to vary in specific volume under the same conditions.

Crystallization Elution Fractionation and Thermal Gradient Interaction Chromatography. Techniques Comparison

AbstractSummary: The chemical composition distribution has been shown to be the most critical and discriminating parameter in understanding the performance of industrial polyolefins with non homogeneous comonomer incorporation. The chemical composition distribution is being analyzed by well known techniques such as temperature rising elution fractionation, TREF, crystallization analysis fractionation, CRYSTAF and crystallization elution fractionation, CEF. These techniques separate according to crystallizability and provide a powerful and predictable separation of components based on the presence of branches, irregularities or tacticity differences, independently of the molar mass. TREF, CRYSTAF and CEF can not be used, however, for the separation of more amorphous resins, and may not always provide the best solution for complex multi‐component resins due to the existence of some co‐crystallization. The application of high temperature interactive HPLC to polyolefins opened a new route to characterize these types of polymers. The use of solvent gradient HPLC for separation of polyethylene and polypropylene and the developments in HPLC on carbon based columns extended further the application of high temperature HPLC in polyolefins. A new approach has been developed recently using the carbon based column but replacing solvent gradient by a thermal gradient which facilitates the analysis of polyethylene copolymers and provides a powerful tool for the analysis of elastomers. Thermal gradient interaction chromatography (TGIC) is being compared with TREF and CEF with the analysis of model samples. The advantages/disadvantages of each technique are being investigated and discussed. The combination of TGIC and TREF/CEF provides an extended range of separation of polyolefins.

High-temperature solvent stability of sol–gel germania triblock polymer coatings in capillary microextraction on-line coupled to high-performance liquid chromatography

Germania-based sol–gel organic–inorganic hybrid coatings were prepared for on-line coupling of capillary microextraction with high-performance liquid chromatography. For this, a germania-based sol–gel precursor, tetra- n-butoxygermane and a hydroxy-terminated triblock copolymer, poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ethylene oxide) were used. These sol–gel germania triblock polymer coatings were chemically anchored to the inner walls of a fused silica capillary (0.25 mm I.D.) in course of its evolution from the sol solution. Scanning electron microscopy images of the sol–gel germania triblock polymer coating were obtained to estimate the coating thickness. For the first time, the analyte distribution constants between a sol–gel germania organic–inorganic hybrid coating and the samples ( K cs) were determined. For a variety of analytes from different chemical classes, including polycyclic aromatic hydrocarbons (PAHs), ketones, alcohols, phenols and amines, the K cs values ranged from 8.1 × 10 1 to 5.6 × 10 4. Also, for the first time, the stability of the sol–gel germania-based coating in high-temperature reversed-phase solvent environment was evaluated. The sol–gel germania triblock polymer coatings were capable of surviving exposure to high-temperature solvent conditions (200 °C) with little change in extraction capabilities. This demonstrates that sol–gel germania triblock polymer hybrid materials might be suitable for further applications in high-temperature HPLC. The reproducibility of the method for preparation of the sol–gel germania triblock polymer coatings was also evaluated, and the capillary-to-capillary RSD values ranged from 5.3 to 6.5%. The use of higher flow rates in extraction was found to significantly reduce the time required (from 30–40 to 10–15 min) to reach equilibrium between the sol–gel germania triblock polymer coating and the analytes in the sample solution.

High-temperature liquid chromatography. Part II: Determination of the viscosities of binary solvent mixtures—Implications for liquid chromatographic separations

This paper is the second in a series of consecutive publications, explaining the concept of high temperature liquid chromatography under various important aspects. The second publication deals with the determination of the viscosity of binary solvent mixtures used in reversed phase liquid chromatography in a temperature range between 25 and 250 °C. In literature, only limited data of the temperature dependent viscosities of liquid solvents or binary solvent mixtures can be found. Therefore, the viscosities of the pure solvents as well as the binary mixtures had to be determined experimentally up to 250 °C. The viscosity data were used to estimate the pressure drop in a capillary connecting a high-temperature HPLC system with a mass spectrometer. The solvent perturbation could be avoided by adjusting the diameter of the transfer capillary to the viscosity and vapour pressure of the mobile phase. The viscosity data were also used to show that a significant gain in analysis speed is theoretically feasible. This factor clearly depends on the nature of the solvent system, because for mixtures with a large viscosity maximum at ambient temperature, this effect is most pronounced.

Separation of Linear Polyethylene from Isotactic, Atactic, and Syndiotactic Polypropylene by High-Temperature Adsorption Liquid Chromatography

For the first time polyolefins are separated according to tacticity by liquid chromatography. High-temperature gradient HPLC is shown to be suitable for the separation of polyethylene and polypropylene. As the stationary phase a porous carbon-based material is used; the mobile phase is composed of 1-decanol and 1,2,4-trichlorobenzene. It is shown that at an operating temperature of 160 °C linear polyethylene as well as syndiotactic and atactic polypropylenes are fully adsorbed on the stationary phase from 1-decanol. In contrast, isotactic polypropylene is fully eluted. This behavior provides a novel way for liquid chromatographic separation of polyolefins. After the isocratic elution of isotactic polypropylene with 1-decanol, all retained components are desorbed from the column packing in a gradient of 1-decanol/1,2,4-trichlorobenzene. Nearly baseline-separated peaks are obtained for all components even in the case where the components do not differ in their molar masses.

Determination of sulfonamides and trimethoprim using high temperature HPLC with simultaneous temperature and solvent gradient

A fast HPLC method for the analysis of eight selected sulfonamides (SA) and trimethoprim has been developed with the use of high temperature HPLC. The separation could be achieved in less than 1.5 min on a 50 mm sub 2 microm column with simultaneous solvent and temperature gradient programming. Due to the lower viscosity of the mobile phase and the increased mass transfer at higher temperatures, the separation could be performed on a conventional HPLC system obtaining peak widths at half height between 0.6 and 1.3 s.

Influence of the stationary phase on the stability of thalidomide and comparison of different methods for the quantification of thalidomide in tablets using high-temperature liquid chromatography

In this paper, three different HPLC methods for the quantification of thalidomide in tablets were developed and compared. The comparison of a conventional method at 30 °C with two high-temperature methods at 180 °C showed equal results. Using high-temperature HPLC (HT-HPLC), faster analysis times could be achieved. We have also focused on analyte stability and could show that the stationary phase has a pronounced effect on the on-column degradation of thalidomide at high temperatures. Virtually no degradation occurs if a polystyrene divinylbenzene column is used, whereas thalidomide is completely degraded at 180 °C when a carbon clad zirconium dioxide column is used.

Separation of Ethylene−Vinyl Acetate Copolymers by High-Temperature Gradient Liquid Chromatography

Ethylene−vinyl acetate (EVA) copolymers can be semicrystalline or amorphous materials, depending on their chemical composition. A variety of different methods were used for the analysis of the chemical composition distribution of these copolymers, which in general were time- and labor-consuming and could be applied only for a limited range of compositions. In the present work a novel chromatographic method is presented that can be used for chemical composition analysis regardless of the composition of the copolymer. High-temperature gradient HPLC has been found to be suitable for chemical composition separation of semicrystalline and amorphous EVA copolymers. In addition, separation is achieved from the respective homopolymers. We have found that gradients of 1,2,4-trichlorobenzene/cyclohexanone, decalin/cyclohexanone, and decalin/1-decanol enable the selective elution of the copolymers from silica gel at 140 °C. The EVA copolymers elute in dependence of their content of the polar vinyl acetate comonomer....

Use of the kinetic plot method to analyze commercial high-temperature liquid chromatography systems: II. Practically constrained performance comparison

Using a set of experimentally determined plate height data obtained on three commercial high-temperature HPLC supports, and evaluating their isocratic separation speed potential under the application of a set of instrumental constraints, a qualitative map of the practically achievable critical pair separation speed potential of high-temperature HPLC has been established. The obtained data show that the gain in separation speed is more strongly affected by the instrumental limitations in the high-temperature range than it is for the low temperatures. For the presently considered case of alkylbenzene separations, the potential gain in analysis time that can be obtained by going from T = 30 to 120 °C in the presence of a typical set of instrumental limitations nevertheless remains of the order of a factor of 2–4. The study also shows that improvements on the instrumentation side (increased detector frequency, pumping flow rate, smaller extra-column volumes, …) are indispensable to fully benefit from the high temperature advantages for all separations requiring less than 10,000 effective theoretical plates.

Use of the kinetic plot method to analyze commercial high-temperature liquid chromatography systems: I: Intrinsic performance comparison

The present study aimed at mapping the separation speed potential of a critical pair on commercial high-temperature HPLC (HT-HPLC) supports at elevated temperatures. For this purpose, band broadening and pressure drop measurements were conducted on three different commercial HT-HPLC columns operated at various elevated temperatures but by keeping the same retention factor. The plate height data were subsequently transformed into a plot showing the minimal required analysis time needed to yield a given required effective plate number. For the considered RPLC alkylbenzene separations, it was found that the maximal gain in separation speed of the critical pair that can be obtained by varying the operating temperature from T=30 to 120°C can be expected to be of the order of a factor of 3–4, if using an individually optimized column length for each considered temperature and if no secondary adsorption effects occur at the lower temperature. This gain factor, remaining more or less constant over the most relevant range of plate numbers, largely paralleled the reduction of the mobile phase viscosity accompanying the temperature increase.

High-temperature gradient HPLC for the separation of polyethylene–polypropylene blends

A high-temperature gradient HPLC method has been developed for the analysis of polyethylene–polypropylene blends. For the first time it was possible to separate these polyolefin blends by a chromatographic technique which is operating at 140 °C. Blends of a commercial polypropylene and a medium molar mass linear polyethylene were separated using a mobile phase of ethylene glycol monobutylether (EGMBE) and 1,2,4-trichlorobenzene (TCB) and silica gel as the stationary phase. With the use of n-decanol as sample solvent, a precipitation–redissolution mechanism for polyethylene (PE) was established while polypropylene (PP) is eluted in size exclusion mode.

Fast, Comprehensive Two-Dimensional HPLC Separation of Tryptic Peptides Based on High-Temperature HPLC

Two-dimensional HPLC (2D-LC) has recently received considerable attention, and is being used as an alternative to 2D gel electrophoresis in proteomics research. The greatest impediment to the widespread use of 2D-LC is the long analysis time ranging up to days per analysis, making the technique impractical for many jobs. Here we focus on improving the speed of gradient separations since these are typically used as the second dimension in peptide separations by 2D-LC. Specifically we describe high-temperature, ultrafast HPLC conditions, along with the instrument modifications needed to reduce the analysis time of each complete second-dimension gradient separation to tens of seconds. Most importantly, this system is capable of generating a high peak capacity (1350) characteristic of comprehensive 2D-LC in a relatively shorter analysis time (20 min) with a sampling rate sufficient to minimize information loss with simpler instrumentation than currently used; this is equivalent to one unit of peak capacity per second.

High temperature fast chromatography of proteins using a silica-based stationary phase with greatly enhanced low pH stability

Reversed-phase liquid chromatography (RPLC) is very widely used for the separation and characterization of proteins and peptides. A novel type of highly stable silica-based stationary phase has been developed for protein separations. A dense monolayer of dimethyl-(chloromethyl)phenylethyl)- chlorosilane (DM-CMPES) on the surface of silica is “hyper-crosslinked” with a polyfunctional aromatic crosslinker through Friedel-Crafts chemistry resulting in stationary phases with extraordinary stability in acidic media. Elemental analysis data confirm the high degree of cross-linking among the surface groups. The hyper-crosslinked phases are extremely stable under highly acidic mobile phase conditions even at a temperature as high as 150 °C. A wide-pore (300 Å) material made in this way is used here to separate proteins by a reversed-phase mechanism and compared to a commercially available “sterically protected” C 18 phase. For small molecules, including neutral and basic compounds, these crosslinked phases give comparable peak shape and efficiency to the commercial phase. Our results show that no pore blockage takes place as commonly afflicts polymer coated phases. In consequence, protein separations on the new phases are acceptable. Using strong ion-pairing reagents, such as HPF 6, improves the separation efficiency. Compared to the commercial phases, these new phases can be used at lower pHs and much higher temperatures thereby enabling much faster separations which is the primary focus of this work. Better efficiency for proteins was obtained at high temperature. However, at conventional linear velocities the instability of proteins at high temperature becomes a problem which establishes an upper temperature limit. Uses of a narrowbore column and high flow rates both solves this problem by reducing the time that proteins spend on the hot column and, of course, speeds up the separation of the protein mixture. Finally, an ultrafast gradient (<1 min) protein separation was obtained by utilizing the high temperature and thus high linear velocities afforded by the extreme stability of these new phases. The phases are stable even after 50 h of exposure to 0.1% TFA at 120 °C. This paper is dedicated to the memory of Csaba Horvath whose work in high temperature HPLC inspired the development of the stationary phases described here.

High-temperature HPLC makes a comeback

High-temperature HPLC makes a comeback

Quantitative NMR-spektroskopische Analyse der Zusammensetzung von Glycerinfettsäureestermischungen

A simple analytical method is described for the determination of glycerol esters of fatty acids based on 13 C-NMR spectroscopy. All ester compounds can be determined in less than 30 min. The NMR method is based on the oxygen influenced carbon atoms of the glycerol fragment providing the molar or the weight percent ratio of the ester mixture. In comparison to established analysis procedures in the field of fat chemistry, like high-temperature gas chromatography or HPLC, the data of the NMR analysis show suitable validation parameters. Additionally, the results of a round robin test are reported.