Abstract: A method and system enable injection of gas into an underground formation, enhanced by the simultaneous injection of liquid. Mixing of the gas and the liquid that have been separately injected into a well comprising two coaxial cylinders can occur at different levels in the well in order to facilitate the flow and to limit the gas pressure necessary for reinjection at the wellhead. Thus, the system and the method require less energy and the associated gas compression equipment is less expensive. The method and system can be applied to geothermal energy applications, underground gas storage, notably CO2, or to enhanced recovery in petroleum reservoirs.

Abstract: The method and the system (100) according to the invention relate to the injection of gas into an underground formation, enhanced by the simultaneous injection of liquid (IL). Mixing of the gas and the liquid can occur at different levels in the well in order to facilitate the flow and to limit the gas pressure necessary for reinjection at the wellhead. Thus, the system (100) and the method require less energy and the associated gas compression equipment is less expensive. The invention notably applies to geothermal energy applications, underground gas storage, notably CO2, or to enhanced recovery in petroleum reservoirs. FIG. 3a to be published.

Abstract: Treatment method for a rock formation against sand infiltration during production of fluid from this rock formation via a well drilled through said rock formation, comprising at least one step of injecting a geopolymer cement grout into said rock formation, in particular around the edges of said well and/or through said well.

Abstract: The present disclosure relates to parenteral nutritional formulations, including ready-to-use parenteral nutrition formulations. More particularly, the present disclosure is directed to lipid formulations or emulsions and multi-chamber containers comprising same, wherein the lipid emulsion contains glycerophosphorylcholine as a choline source. The present disclosure further relates to methods of providing choline to a patient in need of parenteral nutrition and methods of avoiding and/or treating choline deficiency and liver damage.

Abstract: Parenteral nutrition formulations for pediatric patients are disclosed. The nutritional formulations include a lipid formulation that comprises an aqueous phase and an oil phase, wherein the lipid formulation is in the form of an oil-in-water emulsion. Multi-chamber containers for parenteral nutrition administration comprising a carbohydrate formulation present in a first chamber, an amino acid formulation present in a second chamber, and the lipid formulation present in a third chamber also are disclosed.

Abstract: Treatment method for a rock formation against sand infiltration during production of fluid from this rock formation via a well drilled through said rock formation, comprising at least one step of injecting a geopolymer cement grout into said rock formation, in particular around the edges of said well and/or through said well.

Abstract: Process for the separation of a biomolecule containing at least one cationic group from a liquid medium containing the biomolecule, which includes the use of a tetraphenylborate (TPB) salt.

Abstract: Process for the separation of a biomolecule containing at least one cationic group from a liquid medium containing said biomolecule, which comprises the use of a tetraphenylborate (TPB) salt.

Abstract: Process for the separation of a biomolecule containing at least one cationic group from a liquid medium containing said biomolecule, which comprises the use of a tetraphenylborate (TPB) salt.

Abstract: A process for the manufacture of peptide Omiganan in solution phase. Novel intermediates in the process for the manufacture of Omiganan and processes for the manufacture of these intermediates.

Abstract: Described are compounds comprising a peptide moiety linked through a linkage to a short-chain polyethylene glycol moiety, more particularly compounds wherein the peptide moiety comprises a self-assembling peptide sequence, and compositions and hydrogels comprising these compounds. Further, methods for the preparation of the present compounds comprising a peptide moiety linked through a linkage to a short-chain polyethylene glycol moiety are disclosed.

Abstract: A thermo-responsive polymer covalently bound with a peptide, wherein the peptide comprises a peptide moiety that is able to self-assemble and a functional peptide moiety comprising a bioactive sequence, and compositions comprising such thermo-responsive polymer covalently bound with a peptide. Methods for the preparation of such thermo-responsive polymers covalently bound with a peptide and the use thereof for the preparation of hydrogels.

Abstract: Use of the amino acid sequence Har-Gly-Asp (hRGD) as a bioactive sequence in functional peptides to promote cell adhesion, cell growth, and/or cell differentiation, and in the preparation of hydrogels, preferably hydrogels for cell culture. A hydrogel comprising the hRGD sequence, especially a hydrogel wherein the hRGD sequence is part of the hydrogel scaffold.

Abstract: Method for preparing a peptide or a peptide derivative which comprises it least one step in which a free amino acid or a free peptide is reacted with a urethane-protected amino acid N-carboxyanhydride (UNCA) solution.

Abstract: Process for the separation of a biomolecule containing at least one cationic group from a liquid medium containing said biomolecule, which comprises the use of a tetraphenylborate (TPB) salt.

Abstract: A process for the manufacture of peptide Omiganan in solution phase. Novel intermediates in the process for the manufacture of Omiganan and processes for the manufacture of these intermediates.

Abstract: A method is disclosed for modelling low or high compressibility fluid flows in a multilayer porous medium crossed by a network of fractures of given geometry, unevenly distributed in the medium, some of the fractures communicating with one another. Each fractured layer is defined by means of a grid pattern comprising fracture grid cells centered on nodes either at the fracture intersections or at the fracture ends. Each node is associated with a matrix block including all the points closer thereto than to neighboring nodes, and the local flows between each fracture grid cell and the associated matrix volume are calculated in a pseudosteady state. A modelling equation whose form is similar to the diffusion equation solved in conventional cases (low compressibility fluids) allows accounting for the compressibility of the fluids.

Abstract: A method is disclosed for modelling low or high compressibility fluid flows in a multilayer porous medium crossed by a network of fractures of given geometry, unevenly distributed in the medium, some of the fractures communicating with one another. Each fractured layer is defined by means of a grid pattern comprising fracture grid cells centred on nodes either at the fracture intersections or at the fracture ends. Each node is associated with a matrix block including all the points closer thereto than to neighbouring nodes, and the local flows between each fracture grid cell and the associated matrix volume are calculated in a pseudosteady state. A modelling equation whose form is similar to the diffusion equation solved in conventional cases (low compressibility fluids) allows accounting for the compressibility of the fluids.