Description of the technique | EQUIPEMENT | SUMMARY DESCRIPTION OF EQUIPMENT CAPACITIES | Billing Method | University Rates (DH Taxe not included) | Industry Rates EN (DH Taxe not included |
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SYNTHESIS 1 MANUFACTURING | ||||||
THIN FILMS | ||||||
Deposition of thin layers – Metals | PVD-Angstrom Engineering NexDep |
Deposition by evaporation under high vacuum of thin layers of materials having a melting point below 1200 ° C (Aluminum, Silver, chromium, Copper, Gold and fluoridemagnesium).The system is equipped with four resistive sources allowing the co-deposition of layers greater than 1 nm thick. A masking system allows to formpatterns on the sample. | 3 hrs session | 600,00 | 800,00 | |
CHARACTERIZATION | ||||||
SPECTROSCOPY | ||||||
NUCLEAR MAGNETIC RESONANCE (NMR) | Bruker AV600 | NMR spectroscopy is a technique which exploits the magnetic properties of certain atomic nuclei. It is based on the phenomenon of nuclear magnetic resonance.Analysis of liquid, solid, or semi-solid samples allowing the characterization of structures, quality control, and monitoring of the evolution of the different metabolites in bodilyliquids | Sample | 250,00 | 600,00 | |
NUCLEAR MAGNETIC RESONANCE (NMR-2D) | Bruker AV600 | NMR spectroscopy is a technique which exploits the magnetic properties of certain atomic nuclei. It is based on the phenomenon of nuclear magnetic resonance.Analysis of liquid, solid, or semi-solid samples allowing the characterization of structures, quality control, and monitoring of the evolution of the different metabolites in bodilyliquids | Sample | 250,00 | 1 500,00 | |
Spectroscopy inthe UV / Visible / CloseInfrareddomain | Perkin Elmer PE 1050 |
Spectroscopic absorption analysis in the spectral range between the ultraviolet and the near infrared (190 nm to 3300 nm). Liquid or solid samplecan be analyzed in transmission mode or by surface reflection.UV / Visible / NIR spectroscopy is of limited utility for sample identification but ideal for quantitative measurements. UV / Visible / NIR spectroscopy isusually applied to inorganic molecules or complexes in solution. | Sample | 100,00 | 150,00 | |
spectroscopyinfrared (FTIR) | ABB Bomem FTLA2000 |
Spectroscopic absorption analysis in the mid-infrared spectral range.The system accepts liquid or solid samples for analysis in transmission mode.This technique allows the detection of vibrations characteristic of chemical bonds and therefore the identification of functional groups present in the material. | Sample | 100,00 | 150,00 | |
UV fluorescenceDevice | Horiba Yvon Jobin | Spectroscopic analysis of the fluorescence generated by a material following its excitation by absorption of a photon in the ultraviolet range. | Sample | 300,00 | 300,00 | |
CHEMICAL ANALYSIS BY CHROMATOGRAPHY | ||||||
ChromatographyLiquid Phase Coupled withMass spectrometer(UPLC / MS) | Waters Acquity Synapt G2 |
Analysis system based on the separation of the constituent elements of a sample according to their polarity then their identification thanks to their molecular masses. The method also allows direct analysis, withoutseparation in the case of pure products. The method also allows individual analysis by fragmentation of substances. | Sample | 300,00 | 500,00 | |
ChromatographyFizzy Phase Coupled withMass spectrometry(GC / MS) | Agilent GC 7890A |
Analysis system based on the separation of the constituent elements of a sample according to their polarity then their identification thanks to their molecular masses. The method also allows direct analysis, withoutseparation in the case of pure products. The method also allows individual analysis by fragmentation of substances. | Sample | 250,00 | 400,00 | |
MICROSCOPY | ||||||
Scanning Electron Microscope & EDX Analysis | FEI FEG 450 |
Environmental field emission electron microscope (FEG) which allows the observation in very high resolution of all types of solid samples. Materials which are not conductive (oxidized metals, polymers and composites, etc.) can thus be analyzed without the need for metallization or high vacuum.The system is equipped with several types of detectors allowing to extract the maximum of information on the studied material. | 3 hrs session | 300,00 | 700,00 | |
Atomic MicroscopeForce (AMF) | Veeco Dimension ICON |
System for observing and characterizing the surface topology of a sample on an atomic scale. The various accessories make it possible to obtain information on the electrical and magnetic properties of the surface or to carry out measurements in a biological medium or up to 250 ° C. | 4 hrs session | 3 000,00 | 3 000,00 | |
Optical Microscope | Leica | 3 hrs session | 200,00 | 200,00 | ||
CRISTALLOGRAPHY | ||||||
X-ray diffraction -Powder | PANalytical X’Pert |
Determination of the presence of crystalline structures in a sample in the form of powder by X-ray diffraction. The identification of the phases present in a sample is done by comparison of its spectrum(positions and intensities of the diffracted lines) with spectra of known phases. The device is capable of working at 2 Theta angles. | Sample | 150,00 | 350,00 | |
POROUS STRUCTURES / NANOPARTICLE SIZE | ||||||
Micro mesoporosity measurement | Micromeritics 3 Flex |
Determination of specific surface and porosity (volume and distribution) in a wide range of pore sizes from 0.2 to 400 nm. The device iscapable of performing adsorption / desorption isotherms with nitrogen or argon. | Sample | 400,00 | 500,00 | |
Determining the size ofnanoparticles | Malvern Zetasizer ZS |
Determination of the size of nanoparticles in a liquid. The device can also determine the zeta potential which corresponds to the charge of a particle in a particular medium and indicates the stability of a colloidal system. | Sample | 350,00 | 350,00 | |
Determining the size ofparticles – Particle size | Malvern Mastesizer |
Determination of the size of wet or dry particles in a measurement range from 10 nm to 3.5 nm. | Sample | 270,00 | 270,00 | |
THERMAL PROPERTIES | ||||||
Differential calorimetry atscan (DSC) | TA Instrument Q100 |
Measurement of the thermal properties of a material such as latent heat and specific heat. The device can operate in modulated mode allowing to characterize certain irreversible transformations. The device can measure between -80 ° C and 450 ° C. | Sample | 150,00 | 200,00 | |
Thermogravimetric analysis(ATG) | TA Instrument Q500 |
Measurement of the thermal resistance of a material in the presence of an inert or oxidizing atmosphere. The device can heat the sample up to 1000 ° C. | Sample | 150,00 | 150,00 | |
Mechanical Properties | ||||||
MechanicalProperties Measurement | Instron 8821S |
Measurement of the mechanical properties of polymer or composite materials.Three force cells (100 N, 1 kN and 5 kN) are available. | Sample | 350,00 | 350,00 | |
RHEOLOGY | ||||||
Viscosity in the molten state -rotational | ParrPhysica MCR500 |
Measuring the viscoelastic properties of a sample subjected to rotational deformation. The accessories are used to characterize polymers / composites in the molten state or low viscosity fluids. | Sample | 300,00 | 300,00 | |
INTERFACIAL PROPERTIES | ||||||
Contact angle measurement | Data Physics OCA 40 |
Measurement of the contact angle of a liquid. | Sample | 300,00 | 300,00 | |
Interfacial tension measurement | Data Physics DCAT 11 |
Measurement of the surface tension of a material. The device is capable of taking measurements by generating droplets of 2 picoliters. | Sample | 300,00 | 300,00 | |
MAGNETIC PROPERTIES | ||||||
Measurement ofMagnetic Properties under field | LOT Quantum Design MPMS-XL-7AC |
subject to different magnetic field conditions (0 to 7 Tesla) and temperature (1.9 K to 800 K). The system is capable of making measurements at a magnetic field less than 50 mG. | Sample | 1 850,00 | 2 000,00 | |
MICROELECTRONICS | ||||||
CONCEPTION CASE | ||||||
Thermomecanic Simulation | ANSYS / COMSOL |
Numerical simulation by the finite element method. | Simulation | 12 191,00 | ||
Thermal Simulation | ANSYS | Numerical modeling and simulation | Simulation | 12 191,00 | ||
Electromagnetic Simulation | CST | Electromagnetic modeling and simulation | Simulation | 33 400,00 | ||
Design Lay outmechanical BGA | Cadence | Design Lay out Substrate | Batch | 33 400,00 | ||
Injection SimulationMolding | Autodesk moldflow | Simulate injection molding. | Simulation | 14 696,00 | ||
RELIABILITY TEST | ||||||
Thermal Cycling (TC 1000cy) |
Votsch 7012S3 | Perform thermal cycles between two extreme temperatures in a temperature range of – 65 ° C to + 150 ° C | Batch | 14 195,00 | ||
HTS Thermal Storage (168h) | Blue M | Perform fixed temperature thermal storage up to 200 ° C | Batch | 5 848,00 | ||
Acoustic microscopy | SAM 300 | Check the adhesion between the different materials making up the case (resin, die and lead frame) | Batch | 2 550,00 | ||
MSL (Prepackaging +SAT) | Thermal Cycle + Four + SAM |
Moisture sensitivity level test | Batch | 13 360,00 | ||
3D X-Ray | DAGE 7600 NTCT | 3-dimensional x-ray vision | Sample | 2 922,00 | ||
Micro Section | Presi P320 | Mechanical cutting of case and printed circuit | Sample | 1 670,00 | ||
Chemical Opening | Sesame 777Cu | Chemical opening of a part to check the assembly | Sample | 1 253,00 | ||
Pressure Pot (PCT 168h) |
Autoclave | Parts storage at 121 ° C / 100% RH / 1 atm. 168 h | Batch | 7 098,00 | ||
BIOTECHNOLOGY | ||||||
Microbiological analyzes | ||||||
Total aerobic mesophilic flora | Colony count at 30 ° C using the surface seeding techniqueNF EN ISO 4833 NM 08.0.097 (2014) | Sample | 216,00 | 216,00 | ||
Enterobacteriaceae | Search and count using the NPP technique with pre-enrichmentISO 7402 -1993 NM 08.0.106 (2012) | Sample | 250,00 | 250,00 | ||
Salmonella research | Food microbiology: Horizontal method for the detection ofSalmonella spp;NF EN ISO 6579NM 08.0.103 (2012) | Sample | 313,00 | 313,00 | ||
Monocytogenic Listeria | Food microbiology: Horizontal method for the detection and enumeration of Listeria Monocytogens – Part 2: MethodenumerationNF EN ISO 11290NM 08.0.173 (2008) | Sample | 226,00 | 226,00 | ||
Clostridium perfringens | Food microbiology: Enumeration of Clostridium Perfringens by counting colonies at 37 ° C – Routine method;NF V 08-056 / 1994NM 08.0.111 (2003) | Sample | 71,00 | 71,00 | ||
Staphylococcus aureus | Food microbiology: Horizontal method for the enumeration of coagulase-positive staphylococci (Staphylococcus aureus and other species) – Part 1: Technique using Baird-Parker agar medium.NF EN ISO6888-2 / A1NM 08.0.150 (2008) | Sample | 100,00 | 100,00 | ||
Determination of ammoniacal nitrogen | Continuous flow colorimetric methodNM ISO 11732 | Sample | 170,00 | 170,00 | ||
Determination of total nitrogen | Continuous flow colorimetric methodNM ISO 11732 | Sample | 170,00 | 170,00 | ||
Determination of nitrates and nitrites | Continuous flow colorimetric methodNM ISO 13395 | Sample | 170,00 | 170,00 | ||
Determination of nitrites | Continuous flow colorimetric methodNM ISO 13395 | Sample | 170,00 | 170,00 | ||
Boron determination | Azomethine-H spectrometric methodNM ISO 9390 | Sample | 170,00 | 170,00 | ||
Determination of chlorides | By flow analysis (CFA and FIA)NM ISO 15682 | Sample | 170,00 | 170,00 | ||
Determination of fluorides | By flow analysis (FIA and CFA): Method by continuous flow analysis (CFA)ISO / DIS 17951 | Sample | 170,00 | 170,00 | ||
Determination of sodium and potassium | By atomic absorption spectrometryNM 03.7.020- 1990 | Sample | 170,00 | 170,00 | ||
Determination of sulfates | Continuous flow analysis (CFA) methodISO 22743 | Sample | 170,00 | 170,00 | ||
Protein quantification | ||||||
ELISA (direct) | Thermo | A process (enzyme immunosorbent) which allows the determination of antigens (body foreign to the organism) and antibodies thanks to the use of a marker (molecule whose detection makes it possible to identify these elements). In the ELISA method, these markers are enzymes. Direct determination of protein in serum, plasma, culture medium, saliva or tissues. | Sample | 200,00 | 300,00 | |
Gene quantification | ||||||
PCR in real time | ABI 7500 | A very sensitive genitic amplification technique which consists in amplifying a target nucleotide sequence, with each amplification cycle, the quantity of DNA is measured using a fluorescent marker. This production or disappearance of fluorescence measured throughout the amplification cycles is proportional to the quantity of target sequence initially presented, making the process easily quantifiable.This makes it possible to obtain a kinetics of the reaction and therefore thequantification of DNA. Detection or quantification of the fluorescent signal in real time is ensured by means of a TaqMan probe specific for the target sequence to be amplified. | Sample | 300,00 | 300,00 | |
Cell Quantification | ||||||
Flow cytometry(Immunophenotyping 1) | FACSCalibur | Quantify different types of cells in a blood sample and other types of cells.Immunophenotyping: the study of immunological markers. It specifies the antigens present on the surface of blood cells using antibodies conjugated to fluorescence. | Quotation | |||
Cell sorting by flow cytometry | FACSCalibur | Isolation of a type of cells of interest from a cell mixture. | Quotation |