The online combination of reversed-phase liquid chromatography and supercritical fluid chromatography (online RPLC x SFC) is an attractive technique for the characterization of complex samples containing neutral compounds as the two techniques are highly complementary, especially with a polar stationary phase in supercritical fluid chromatography (SFC). However, the setup is challenging due to the presence of hydro-organic solvents in RPLC, which become injection solvent in SFC. In this study, numerous key experimental parameters were identified and found to have a major effect on peak shape under RPLC x SFC conditions. These parameters included the organic modifier in reversed-phase liquid chromatography (RPLC), the co-solvent in SFC, the gradient conditions and the column ID in SFC, the configuration of the valve and finally, the injection volume in SFC that should be maximized. Acetonitrile (ACN) in RPLC, a mixture of ACN and methanol (MeOH) (50/50, v/ v) in SFC, a minimum initial composition of 5% B in SFC, column IDs of 1.0 mm and 2.1 mm in RPLC and SFC respectively and flushing the interface loops with pure CO2 while adding the co-solvent after the valve, are all conditions that have been identified as perfectly suitable for online RPLC x SFC. They were successfully applied to the online RPLC x SFC separations of microalgae bio-oil samples. Despite unusual injection conditions, the peaks were symmetrical over the entire chromatogram, leading to a high separation power.

Une analyse par spectrométrie de masse à résonance cyclotronique (FT-ICR MS) a été réalisée en utilisant l’ionisation par électronébulisation (ESI) dans les modes positifs et négatifs pour caractériser une bio-huile issue de la pyrolyse du bois de hêtre (PBO) produite dans un réacteur à lit fluidisé. L’analyse a révélé une composition moléculaire complexe de la bio-huile, avec une prédominance notable de composés oxygénés. La comparaison des modes d’ionisation positifs et négatifs a démontré des variations moléculaires, indiquant que le mode positif offre une caractérisation plus complète de la bio-huile. L’étude souligne l’importance de choisir la technique d’ionisation appropriée pour caractériser pleinement la diversité chimique des bio-huiles, ce qui permettra de mieux déterminer leur composition et d’optimiser leur application potentielle.

Microalgae are an attractive feedstock for biofuel production thanks to their renewable nature, high growth rate, and ability to use anthropogenic CO2. The conversion of microalgae by hydrothermal liquefaction (HTL) leads to a solid residue, a gaseous phase, and a biocrude. However, the bio-oil is rich in heteroatoms and requires upgrading processes to be used as biofuels. For these treatments to be effective, detailed knowledge of the sample is crucial. The bio-oil was characterized by direct introduction into a Fourier transform ion cyclotron resonance mass spectrometer (DI-FTICR MS) with an electrospray ionization source (ESI). Thousands of molecular formulas were assigned with a high level of confidence, mainly compounds with nitrogen and oxygen atoms. Additionally, the bio-oil was analyzed by coupling supercritical fluid chromatography (SFC) and FTICR to combine the separation power of SFC to the high performances of a 12 T FTICR. Quadrupole detection (2 omega) was used in FTICR to have a high resolving power with a lower transient time. The coupling allowed the separation of many isomers along the chromatogram, showing the isomeric complexity of microalgae bio-oils. Moreover, classes of compounds were separated according to their heteroatom class thanks to the SFC separation. In this work, the advantages of DI-FTICR MS and SFC-FTICR MS proved complementary, and DI was useful to study the bio-oil at the molecular scale thanks to the high performances, while SFC proved useful for the characterization at the isomeric scale. This demonstrated the significant potential of this new online hyphenated technique for the characterization of complex matrices.

Bio-oils obtained by thermochemical or biochemical conversion of biomass represent a promising source of energy to complement fossil fuels, in particular for maritime or air transport for which the use of hydrogen or electricity appears complicated. As these bio-oils are very rich in water and heteroatoms, additional treatments are necessary before they can be used as biofuel. In order to improve the efficiency of these treatments, it is important to have a thorough knowledge of the composition of the bio-oil. The characterization of bio-oils is difficult because they are very complex mixtures with thousands of compounds covering a very wide range of molecular weight and polarity. Due to the high degree of orthogonality between the two chromatographic dimensions, the on-line combination of reversed-phase liquid chromatography and supercritical fluid chromatography (on-line RPLC x SFC) can significantly improve the characterization of such complex matrices. The hyphenation was optimized by selecting, in SFC, the stationary phase, the co-solvent, the make-up solvent prior to high resolution mass spectrometry (HRMS) and the injection solvent. Additionally, a new interface configuration is described. Quality descriptors such as the occupation of the separation space, the peak shapes and the signal intensity were considered to determine the optimal conditions. The best results were obtained with bare silica, a co-solvent composed of acetonitrile and methanol (50/50, v/v), a make-up solvent composed of methanol (90%) and water (10%) with formic acid (0.1%), an addition of co-solvent through an additional pump for SFC separation in a 2.1 mm column, and an hydro-organic solvent as injection solvent. The optimized setup was used to analyze two microalgae bio-oils: the full bio-oil coming from hydrothermal liquefaction and Soxhlet extraction of microalgae, and the gasoline cut obtained after distillation of the full bio-oil. Results in online RPLC x SFC-qTOF were particularly interesting, with very good peak shapes and high reproducibility. Moreover, the high degree of orthogonality for microalgae bio-oils of RPLC and SFC was highlighted by the very large occupation of the separation space. Isomeric profiles of compound families could be obtained in RPLC x SFC-qTOF and many isomers not separated in SFC alone were separated in RPLC and vice versa, thus showing the complementarity of the two chromatographic techniques.(c) 2023 Elsevier B.V. All rights reserved.