Abstract: The present invention relates to a method for extracting organic molecules and/or organic minerals from a limestone material, including placing said limestone material in contact with a solution including at least one organic solvent, water and at least one acid, as well as to the organic molecules and/or organic minerals produced by the method. The products produced by the method can be used, for example, in therapeutic and non-therapeutic fields, in particular the agri-food, cosmetic and medical fields.

Abstract: This method comprises the steps of: transmitting a beam of light onto a surface (17) of an element (1) comprising a fissile material, passing the beam of light reflected by the surface into a polarisation analyser (27) having a modifiable analysis direction, transmitting the beam from the polarisation analyser (27) to a device (31) for acquiring digital images, acquiring at least one digital image (31) of the surface (17) of the element (1) and processing the digital image acquired in order to measure the anisotropy. Use, for example, in controlling particles of nuclear fuel for an HTR/VHTR type reactor.

Abstract: This method comprises the steps of transmitting a beam of light onto a surface (17) of an element (1) comprising a fissile material, passing the beam of light reflected by the surface into a polarisation analyser (27) having a modifiable analysis direction, transmitting the beam from the polarisation analyser (27) to a device (31) for acquiring digital images, acquiring at least one digital image (31) of the surface (17) of the element (1) and processing the digital image acquired in order to measure the anisotropy. Use, for example, in controlling particles of nuclear fuel for an HTR/VHTR type reactor.

Abstract: The invention relates to a fluid preparation method comprising the recovery of the fluid that is located between the shell and the body of a mollusc. The invention also relates to the liquid obtained using said method, and to the use thereof in the pharmaceutical field, in particular in order to improve cutaneous healing, to regenerate tissues or to promote osteogenesis or bone mineralization. The invention further relates to compositions, particularly pharmaceutical compositions, medical devices or food supplements containing same.

Abstract: The present invention relates to: a novel process for the preparation of mesophasic polyborazylene. Said process is of particular value in that it affords a quality product from an appropriate polyborazylene, rapidly (virtually instantaneously), reproducibly and with a good yield. Furthermore, said process is easy to carry out. Said process comprises the preparation of polyborazylene by the polycondensation of borazine in a closed reactor and the addition, to said polyborazylene obtained by polycondensation, of a solvent selected from aromatic solvents, borazine solvents and mixtures thereof, mesophasic polyborazylene which is novel in that it is in the presence of a particular solvent and/or by virtue of its quality, the use of said polyborazylene of the invention, and/or prepared according to the invention, as a boron nitride precursor.

Abstract: The pyrolytic carbon lamellar interphase is formed on the reinforcing fibers inside a chamber in which a plurality of successive cycles is performed, each cycle comprising: injecting a reaction gas in which the pyrolytic carbon precursor is selected from alkanes, excluding methane taken as a sole component, alkenes, alkynes, and aromatic hydrocarbons, and mixtures thereof; the gas is maintained inside the chamber for a first predetermined time period to form an interphase layer of controlled thickness of nanometer size; the gaseous reaction products are then evacuated during a second time period; the cycles being performed consecutively in the chamber until the thickness desired for the interphase has been obtained, thereby achieving a lamellar interphase that is highly anisotropic, whose lattice fringe texture has distorted fringes of total length (L.sub.2) not less than 4 nanometers on average with maximum values exceeding 10 nanometers.

Abstract: The pyrolytic carbon lamellar interphase is formed on the reinforcing fibers inside a chamber in which a plurality of successive cycles is performed, each cycle comprising: injecting a reaction gas in which the pyrolytic carbon precursor is selected from alkanes, excluding methane taken as a sole component, alkenes, alkynes, and aromatic hydrocarbons, and mixtures thereof; the gas is maintained inside the chamber for a first predetermined time period to form an interphase layer of controlled thickness of nanometer size; the gaseous reaction products are then evacuated during a second time period; the cycles being performed consecutively in the chamber until the thickness desired for the interphase has been obtained, thereby achieving a lamellar interphase that is highly anisotropic, whose lattice fringe texture has distorted fringes of total length (L.sub.2) not less than 4 nanometers on average with maximum values exceeding 10 nanometers.