In manufacturing processes, the quality of a product often depends on its surface, and careful control of surface properties is critical to meet customer requirements. A thin layer of polyethylene (PE) is applied to paperboard to increase barrier functionality and high optical quality of the product. For PE-coated paperboard, product quality inspection is performed at the end of the manufacturing process by taking a portion of the reel to the laboratory for quality inspection. These associated offline characterization methods are destructive and time consuming and are representative of only a small portion of the product. The overall goal of this thesis is to provide new methods to characterize the Surface properties of PE-coated paperboard. Specifically, to determine imaging techniques for measuring surface parameters that affect its barrier functionality and surface roughness. In this thesis, two methods for surface characterization of PE-coated paperboard are presented to quantify the two most important product-related quality parameters, i.e. barrier functionality and optical quality, which are affected by the presence of defects in the coating and by the surface roughness of the product, respectively. First, a full-Stokes imaging polarimeter (FSIP) is used to detect the presence of PE-coated material and to distinguish between coated and uncoated samples at the pixel level. Second, a three-dimensional scanning electron microscope (3D SEM) is employed to calculate the Surface roughness of PE-coated paperboard. These surface characterization techniques offer an advantage over the industry standard due to the high speed and non-contact nature of the measurement, while increasing the throughput of the sample surface parameters studied. A classification accuracy of 99, 74% is achieved using a FSIP to distinguish between PE- and non-PE-coated paperboard at pixel level. Using the 3D SEM technique to measure the topography of PE-coated samples results in a faster method that is comparable in accuracy to a chromatic confocal microscope (CCM). The surface roughness measured with the 3D SEM differs from the standard method by up to 6% and good agreement with statistical parameters is found. In general, surface analysis of PE-coated is often a complex and difficult task for imaging techniques and suitable methods need to be evaluated for their sensitivity to measure the desired surface parameters. The presented characterization techniques inspect larger areas of PE-coated paperboard compared to current industry standards. These methods provide a quantitative solution for surface characterization to inspect the surface parameters necessary to assure the product’s quality.

Absolicon is a pioneering solar technology development company specializing in the manufacturing and selling of advanced solar energy systems engineered to generate renewable energy for diverse use. Comprising essential components such as reflectors (mirrors) and a solar receiver tube, these solar energy systems are equipped to efficiently capture and convert solar irradiation into usable thermal energy. As an integral facet of an ongoing research, this project will contribute to optimize the reflection and absorption capacity in receiver tubes of Absolicon's solar collectors. The aim is to investigate optically selective plasmonic coatings intended as an undercoating in the solar selective surfaces. The main coating material that will be used and analysed is gold due to its plasmonic properties and inert nature as well as its low toxicity. The gold will be coated on stainless steel using physical vapor deposition (PVD) and then annealed at mid-to-high temperatures to produce a plasmonic surface. The effect of Au thicknesses, annealing times/temperature and will be investigated to optimize the coating with regards to optical properties based on a systematic method called Design of Experiments (DoE). The goal for the gold coating is to increase the reflectance in the infrared region while generating a plasmonic absorption peak in the visible region (the position and width will be optimized), making it a more beneficial surface to coat a solar selective surface than the original stainless steel (SS). It was found that the size and inter-particle distance of GNPs depend on the temperature and annealing time for different thickness. The surface analysis from SEM-images and AFM-topographs provided that samples with smaller grains are more likely to exhibit significant plasmonic effects compared to larger grains. According to the surface characterization, either thinner gold coating exposed to high temperature for short annealing time or thicker gold coating with longer annealing time provide plasmonic absorption peak in visible light region.

Die Mechanochemie ist eine effekive und überzeugende Methode zur Herstellung von Alumniumhydroxidfluoriden (Al(OH)3-xFx) mit einem sehr geringen Fluorgehalt. Durch den Prozess des Mahlens werden strukturelle Defekte in den Kristalliten erzeugt, die zu einer zunehmenden Amorphisierung des Kristallsystems führen. Die partielle Fluorierung von Alumniumhydroxid während des Mahlprozesses führt dabei zu einer noch stärkeren Amorphisierung und zur Bildung von Alumniumhydroxyfluoriden. Eine wichtige Rolle bei der resultierenden Produktzusammensetzung spielt die Variation der Synthesebedingungen, wie der Grad der Fluorierung, der Dauer des Mahlprozesses und des Wassergehalt der Edukte. Folglich wurde zuerst der Einfluss von Wasser und dessen Bedeutung durch die verschiedenen Kombinationen von Oxid- und Hydroxid- (Al(OH)3, Al2O3), sowie Fluorid-Quellen mit oder ohne Kristallwasser (β-AlF3.3H2O, α-AlF3) bei der mechanochemischen Synthese von hochgestörten Alumniumhydroxidfluoriden untersucht. Um den optimalen Fluorierungsgrad zu ermitteln, wurden verschiedene Aluminiumhydroxidfluoride mit Al/F-Molverhältnissen von 1:1.5 bis 1:0.05 über die mechanochemische Syntheseroute hergestellt. Eine tiefergehende Charakterisierung der Struktur- und Oberflächeneigenschaften der entsprechenden Produkte erfolgte mittels XRD, 27Al- und 19F-Festkörper-NMR, thermischer Analyse, Stickstoffabsorptions- und Zeta Potentialmessungen. Mit γ-Al(OH)3 und β-AlF3•3H2O als Hydroxid- und Fluorid-Quellen wurden dabei ab einem Verhältnis Al:F von 1:0.25 und hin zu höheren Fluoridanteilen besonders ungeordnete Strukturen erzeugt. Der Fluorierungsgrad betrifft dabei besonders die Ausbildung von 4- und 5-fach koordinierten Al-Zentren, die sonst nicht in den Edukten vorkommen. Diese Spezies beeinflussen die Bildung von Alumniumoxid und ermöglichen den Phasenübergang zu α-Al2O3 schon bei tieferen Temperaturen. Der Einfluss der Mahldauer auf die Struktur und Oberfläche wurde am Beispiel von γ-Al2O3 im Detail untersucht. Die mechanochemische Synthese beeinflusst dabei die Absorption von Fluor an der Grenzschicht von γ-Al2O3 zu Wasser stark. Die Dauer des Mahlprozesses gewinnt daher einen großen Einfluss auf die entstehenden Produkte. Da Fluor nicht im Bulk von γ-Al2O3 vorkommt, kann mit der 19F-Festkörper-NMR eine Zuordnung der unterschiedlichen an der Oberfläche adsorbierten F-Spezies getroffen werden. / The mechanochemical approach opens a reliable and effective strategy for the formation of aluminium hydroxide fluorides with a very low F-content. Milling has the effect of introducing structural defects, causing amorphisation. The fluorination by milling creates a further and drastic increase of this degree of amorphisation. Synthesis conditions (milling time, fluorination degree, water content) play a crucial role in the product composition. Firstly, the significant role played by water in the mechanochemical synthesis of highly distorted aluminium hydroxide fluorides was evaluated. The importance of water in the synthesis was considered by a separated combination of O/OH sources (Al(OH)3, Al2O3) and fluorine sources with or without structural water (β-AlF3.3H2O, α-AlF3). Concerning the degree of fluorination, different aluminium hydroxide fluorides with varying Al/F molar ratios from 1:1.5 up to 1:0.05 were successfully synthesized by mechanochemical reactions. The characterization of the products by XRD, 27Al and 19F MAS NMR, thermal analysis, nitrogen adsorption and zeta potential techniques allows a detailed understanding of the structure and surface properties of the products. Using γ-Al(OH)3 and β-AlF3•3H2O as OH- and F-sources, respectively, strongly disordered products were obtained with an Al: F molar ratio higher than 1:0.25. The degree of fluorination affects the amount of 4- and 5-fold coordinated Al sites, not present in the reactants. Obviously, these species affect the phase transition to alumina, by decreasing the transition temperature of the formation of α-Al2O3. The influence of the milling time was considered by studying the power of a high energy ball milling process on the structure and at the surface of γ-Al2O3. The mechanochemical treatment strongly influences the adsorption of fluorine at the γ-Al2O3/ water interface. The time of the treatment has relevant importance on these processes. Since fluorine is not originally present in the bulk of γ-Al2O3, 19F MAS NMR studies allow the discrimination of different F-species adsorbed at the surface or present as metal fluoride particles in γ-Al2O3 powders after adsorption experiments.

In der vorliegenden Arbeit wurden das Wachstum und die Oberflächenstruktur von definier-ten V2O3-, V2O5- und MoO3-Filmen auf Au(111) sowie deren Einsatz als Modellsysteme zur Untersuchung von Elementarreaktionen auf Vanadiumoxid- und Molybdänoxid-basierten selektiven Oxidationskatalysatoren untersucht. Im Falle von V2O3(0001) befindet sich an der Oberfläche der Filme eine Lage von Vanadylgruppen, welche kein Bestandteil der Kristall-struktur sind. Die O Atome der Vanadylgruppen können durch Elektronenbeschuss definiert entfernt werden, wodurch eine partiell oder vollständig V-terminierte Oberfläche erzeugt werden kann. Der Grad der Oberflächenreduktion wird durch die Elektronendosis festgelegt. Dieses ermöglicht eine Untersuchung des Einflusses der Vanadylgruppen und der unterkoor-dinierten V-Ionen auf die Reaktivität der Modellkatalysatoren. Die Präparation von defektar-men V2O5(001)- und MoO3(010)-Filmen ist erstmals in der vorliegenden Arbeit dokumen-tiert. Diese Filme wurden mittels Oxidation in einer Hochdruckzelle bei einem Sauerstoffdruck von 50 mbar hergestellt. Anders als in vielen Publikationen berichtet sind diese hochkristallinen Schichten unter UHV-Bedingungen weitgehend reduktionsbeständig. Oberflächenverunreinigungen und Defekte scheinen aber einen großen Einfluss auf die Redu-zierbarkeit zu haben. Die von den Strukturen der regulären Oxide abweichenden Strukturen der Koinzidenzgitter von V2O5- und MoO3-Monolagen werden durch die Wechselwirkung mit der Au(111)-Unterlage stabilisiert, was vermutlich durch die einfache Verschiebbarkeit von Koordinationseinheiten in V und Mo-Oxiden erleichtert wird. Für beide Oxide beginnt das Wachstum regulärer Oxidstrukturen erst nach Vollendung der zweiten Lage. Die für geträgerte V2O5-Katalysatoren häufig vorgebrachte Annahme, dass V2O5-Kristallkeimbildung direkt auf einer Monolage stattfindet, sollte somit mit Vorsicht betrachtet werden. / The growth and the surface structure of well-ordered V2O3, V2O5 and MoO3 thin films have been investigated in this work. These films are seen as model systems for the study of ele-mentary reaction steps occurring on vanadia and molybdena-based selective oxidation cata-lysts. It is shown that well-ordered V2O3(0001) thin films can be prepared on Au(111). The films are terminated by vanadyl groups which are not part of the V2O3 bulk structure. Elec-tron irradiation specifically removes the oxygen atoms of the vanadyl groups, resulting in a V-terminated surface. The fraction of removed vanadyl groups is controlled by the electron dose. Such surfaces constitute interesting models to probe the relative role of both the vanadyl groups and the undercoordinated V ions at the surface of vanadia catalysts. The growth of well-ordered V2O5(001) and MoO3(010) thin films containing few point defects is reported here for the first time. These films were grown on Au(111) by oxidation under 50 mbar O2 in a dedicated high pressure cell. Contrary to some of the results found in the literature, the films are not easily reduced by annealing in UHV. This evidences the contribution of radiation and surface contamination in some of the reported thermal reduction experiments. The growth of ultrathin V2O5 and MoO3 layers on Au(111) results in formation of interface-specific monolayer structures. These layers are coincidence lattices and they do not correspond to any known oxide bulk structure. They are assumed to be stabilized by electronic interaction with Au(111). Their formation illustrates the polymorphic character and the ease of coordination units rearrangement which are characteristic of both oxides. The formation of a second layer apparently precedes the growth of bulk-like crystallites for both oxides. This observation is at odds with a common assumption that crystals nucleate as soon as a monolayer is formed dur-ing the preparation of supported vanadia catalysts.

Graphene has been shown to be very powerful as a transducer in many biosensor applications due to its high sensitivity. This enables smaller surfaces and therefore less material consumption when producing sensors and concequently cheaper and more portable sensors compared to the commercially available sensors today. The electrical properties of graphene are very sensitive to gas exposure why presence of molecules or small changes in concentration could easily be detected when using graphene as a sensing layer. Graphene is sensitive towards many molecules and in order to detect and possibly identify gas molecules the surface needs to be functionalized. The intention of this project was to use nanoparticles (NPs) to further increase sensitivity and specificity towards selected molecules and also enable biofunctionalization of the NPs, and by that tune the electrical properties of the graphene. This study proposes the use of Fe3O4 and TiO2 NPs to enable sensitive detection of volatile gases and possibly further functionalization of the NPs using biomolecules as a detecting agent in a liquid-phasebiosensor application. The interaction between graphene and NPs have been investigated using several surface charactarization methods and electrical measurements for detection of gaseous molecules and also molecules in a liquid solution. The characterizing methods used are XPS, AFM with surface-potential mapping and Raman spectroscopy with reflectance mapping in order to investigate the NPs interaction with the graphene surface. Sensors where manufactured for gas-phase detection of CO, formaldehyde, benzene and NH3 specifically and display differences in sensitivity and behavior of the Fe3O4 and TiO2 NPs respectively. For liquid measurements the difference in behavior in two buffers was investigated using an in-house flow-cell setup. The surface charecterizing measurements indicated that just a small difference could be found between the two NPs, however a significant change in sensor response could be detected as a function of coverage. The liquid and gas-phase measurements rendered information on differences in sensitivity between the NPs and between analytes where TiO2 showed a higher level of sensitivity towards most of the gases investigated. Both Fe3O4 and TiO2 NP coated graphene showed capability to detect formaldehyde and benzene down to 50 ppb and 5 ppb respectively. The sensitive gas detection could help protecting individuals being exposed to a hazardous level of volatile gases if concentrations increase rapidly or at a long term exposure with lower concentrations, improving saftey and health where these gases are present.

Notre thèse s’inscrit dans le cadre de la compréhension des mécanismes d’inactivation de microorganismes, principalement des spores bactériennes, suite à un traitement à l’ozone. Les objectifs généraux, au départ, étaient de mettre en place une stratégie expérimentale dans le but de déterminer les espèces et les phénomènes impliqués dans les mécanismes d’inactivation des spores en combinant diverses techniques pluridisciplinaires. Rappelons que les récentes avancées en stérilisation par plasma sont principalement dues aux études menées sur les mécanismes d’inactivation des microorganismes. Dans ce contexte, en nous appuyant sur une synthèse des études publiées dans la littérature scientifique, nous avons élaboré une étude expérimentale en deux étapes : l’étude de la stérilisation à l’ozone en milieu sec puis en milieu humide. Au cours de ces études, nous avons principalement étudié la cinétique d’inactivation des microorganismes, les dommages occasionnés à ces derniers par de tels traitements et nous avons identifié les espèces responsables de l’inactivation pour, enfin, proposer un mécanisme d’inactivation en spécifiant le rôle et l’importance des différents phénomènes en jeu. L’originalité de notre approche s’appuie sur la corrélation faite entre ces deux types de traitement (ozone sec et humidifié) ainsi que la diversité et la complémentarité des moyens de caractérisation utilisés. Dans un second volet, nous avons mis en évidence pour la première fois la possibilité de conférer à une surface de Pétri de polystyrène (PS) une importante activité biocide suite à un traitement à l’ozone. Nous avons mené une étude de caractérisation des propriétés de ces surfaces démontrant, principalement, leur grande efficacité biocide sur une large gamme de microorganismes, l’importance de l’interaction microorganismes/surface traitée, l’existence de la rémanence biocide, les modifications physico-chimiques induites en surface… L’étude des modifications physico-chimiques et microbiologiques nous a permis d’approcher les mécanismes d’inactivation en identifiant, de manière non exhaustive, les phénomènes impliqués. Enfin, nous avons examiné l’applicabilité de cette méthode à divers types de polymères montrant que le degré d’activité biocide induite dépend de la nature du substrat. / The thesis deals with the inactivation mechanisms of microorganisms (mainly endospores) after an ozone treatment. The general objective of this work was to provide an experimental strategy to identify the phenomena and chemical species involved in microorganism inactivation mechanism using multidisciplinary techniques. Recall that the recent advances in plasma sterilization are mainly due to comprehensive studies dealing with the inactivation mechanisms of microorganisms. In this context, based on a review of published studies, we proposed a two-step experimental study of ozone sterilization in both dry and humid media. In the course of this work, we have examined the inactivation kinetics of some microorganisms, their damage after treatments; we have also identified the chemical species responsible for inactivation, and proposed an inactivation mechanism (for each type of ozone treatment) by describing the importance and role of the different implicated phenomena. The originality of our approach rests on the correlation achieved between the dry and humid ozone treatment, and by the diversity and complementarity of the characterization techniques used. In a second part, we show for the first time the possibility to confer biocide activity to surfaces of polystyrene (PS) Petri dishes after their exposure to ozone. A characterization study of these treated surfaces mainly shows a high inactivation efficacy on various microorganisms, the importance of the microorganisms/treated-surface interaction, the biocide persistence of the treated surfaces and physico-chemical modifications. The study on physico-chemical and microbiological changes gives us elements for identifying the phenomena involved in the inactivation mechanisms. Finally, we have shown the possibility to confer biocide properties to polymeric surfaces in general with the same experimental process observing that the biocide efficacy depends on the nature of the polymer. / Une partie du travail a mené a un dépôt de brevet.

La caractérisation de la proche surface est un enjeu majeur pour l'industrie pétrolière. Lors des acquisitions terrestres et Ocean Bottom Cable (OBC), les couches superficielles généralement altérées ou peu consolidées, présentent des structures géologiques complexes et ont éventuellement des variations topographiques importantes. Les ondes de surface, énergétiques, se propagent dans ce milieu complexe et dominent les sismogrammes, ce qui masque le signal utile pour le traitement sismique classique et rend difficile l'imagerie à la profondeur du réservoir.Il est donc important de pouvoir atténuer ces ondes, éventuellement d'appliquer des corrections statiques et/ou d'amplitude. Ceci qui nécessite une connaissance précise du modèle de vitesse de la proche surface. L'étude de la dispersion des ondes de surface est couramment utilisée en sismologie globale et à l'échelle géotechnique pour évaluer les propriétés des milieux terrestres. Il existe néanmoins des limitations: la mesure de cette dispersion est souvent difficile et les profils de vitesses obtenus sont 1D. A l'échelle pétrolière, l'hypothèse 1D n'est pas toujours adaptée, ce qui motive l'utilisation d'une méthode alternative d'imagerie plus haute résolution, la méthode d'inversion de la forme d'onde (FWI). Cependant, le modèle de vitesse initial doit être assez précis pour éviter le "cycle-skipping" et permettre la convergence vers la solution optimale.Cette étude explore différentes alternatives de fonctions coûts pour résoudre le "cycle-skipping" et diminuer la dépendance de l'inversion à la qualité du modèle initial. En exprimant les fonctions coûts dans le domaine f-k (fréquence-nombre d'onde) et le domaine f-p (fréquence-lenteur), la FWI est plus robuste. A l'aide d'exemples synthétiques, nous démontrons l'efficacité de ces nouvelles approches qui permettent bien de retrouver les variations latérales de vitesses d'onde S.Dans une seconde partie, nous développons une inversion FWI en "layer stripping", adaptée spécifiquement à la physique des ondes de surface. Comme la profondeur de pénétration de ces ondes dépend de leur longueur d'onde, et donc, de leur contenu fréquentiel, nous proposons d'inverser séquentiellement des plus hautes aux plus basses fréquences de ces ondes pour contraindre successivement les couches superficielles jusqu'aux plus profondes. Un fenêtrage selon la distance source-station est également appliqué. Dans un premier temps seules les courtes distances sont inversées, au fur à mesure les données associées à des plus grandes distances sont rajoutées, plus fortement impactées par le "cycle-skipping". Nous démontrons à l'aide d'exemples synthétiques l'avantage de cette méthode par rapport aux méthodes multi-échelles conventionnelles inversant des basses vers les hautes fréquences.Enfin, l'inversion des ondes de surface pour la caractérisation de la proche surface est confrontée à un cas réel. Nous discutons la construction et la pertinence du modèle initial et les difficultés rencontrées lors de l'inversion. / The characterization of the near surface is an important topic for the oil and gas industry. For land and Ocean Bottom Cable (OBC) acquisitions, weathered or unconsolidated top layers, prominent topography and complex shallow structures may make imaging at target depth very difficult. Energetic and complex surface waves often dominate such recordings, masking the signal and challenging conventional seismic processing. Static corrections and the painstaking removal of surface waves are required to obtain viable exploration information.Yet surface waves, which sample the near surface region, are considered as signal on both the engineering and geotechnical scale as well as the global seismology scale. Their dispersive property is conventionally used in surface wave analysis techniques to obtain local shear velocity depth profiles. But limitations such as the picking of dispersion curves and poor lateral resolution have lead to the proposal of Full Waveform Inversion (FWI) as an alternative high resolution technique. FWI can theoretically be used to explain the complete waveforms recoded in seismograms, but FWI with surface waves has its own set of challenges. A sufficiently accurate initial velocity model is required or otherwise cycle-skipping problems will prevent the inversion to converge.This study investigates alternative misfit functions that can overcome cycle-skipping and decrease the dependence on the initial model required. Computing the data-fitting in different domains such as the frequency-wavenumber (f-k) and frequency-slowness (f-p) domains is proposed for robust FWI, and successful results are achieved with a synthetic dataset, in retrieving lateral shear velocity variations.In the second part of this study a FWI layer stripping strategy, specifically adapted to the physics of surface waves is proposed. The penetration of surface waves is dependent on their wavelength, and therefore on their frequency. High-to-low frequency data is therefore sequentially inverted to update top-to-bottom layer depths of the shear velocity model. In addition, near-to-far offsets are considered to avoid cycle-skipping issues. Results with a synthetic dataset show that this strategy is more successful than conventional multiscale FWI in using surface waves to update the shear velocity model.Finally inversion of surface waves for near surface characterization is attempted on a real dataset at the oil and gas exploration scale. The construction of initial models and the difficulties encountered during FWI with real data are discussed.

No description available.

Ce travail s’inscrit dans le cadre général du développement de biomatériaux ostéoinducteurs pour la réparation de grands défauts osseux. L’étude est une contribution à la compréhension des interactions physiques et chimiques entre des céramiques phosphocalciques et deux protéines d’intérêt : la fibronectine, protéine d’adhésion cellulaire, et le VEGF (pour Vascular Endothelial Growth factor) qui est impliqué dans la vascularisation et l’amélioration de la formation osseuse.Les interactions physiques fibronectine/biocéramique ont été étudiées par spectroscopie de force afin d’évaluer l’influence de la topographie et de la composition chimique de céramiques phosphocalciques en hydroxyapatite (HA), hydroxyapatite silicatée (SiHA) et hydroxyapatite carbonatée (CHA) sur l’adhésion de la fibronectine. Les résultats obtenus par cartographie de forces mettent en évidence une absence d’incidence de la chimie des céramiques polies sur la répartition en surface et l’intensité des forces d’adhésion. En revanche ces dernières sont plus fortes au niveau des joints de grains des céramiques non polies mettant en avant une influence de la topographie de surface des matériaux modulée par la chimie.Le protocole de fonctionnalisation par le VEGF consiste en trois étapes : silanisation, addition du SM(PEG)6 et immobilisation du VEGF. Les interactions chimiques VEGF/biocéramique ont été étudiées principalement par imagerie Raman pour suivre ces étapes successives de la fonctionnalisation par le VEGF de céramiques polies en hydroxyapatite (HA) et hydroxyapatite carbonatée (CHA). Cette approche a permis de cartographier l’évolution chimique de la surface des matériaux et de mettre en évidence la distribution spatiale ainsi que les réactions préférentielles entre les molécules intermédiaires et le VEGF en fonction de la nature du substrat. / This work is ascribed within the framework of the development of osteoinductive biomaterials for the repair large bone defects. It is a contribution to the understanding of the physical and chemical interactions between phosphocalcic ceramics and two proteins of interest: fibronectin (Fn), a cell adhesion protein, and Vascular Endothelial Growth Factor (VEGF) which is involved in vascularisation and improvement of bone formation.Fibronectin/bioceramic physical interactions were studied by force spectroscopy to evaluate the influence of the topography and the chemical composition of phosphocalcic ceramics made of hydroxyapatite (HA), silicated hydroxyapatite (SiHA) and carbonated hydroxyapatite (CHA) on fibronectin adhesion. The results obtained in terms of force cartography do not indicate any impact of the polished ceramics chemistry on the surface distribution and intensity of adhesion forces. However, these forces are more intense at the level of the grain boundaries of unpolished ceramics, highlighting an influence of the topography modulated by the chemical composition.The protocol for functionalisation by VEGF consists of three steps: silanisation, addition of SM(PEG)6 and immobilisation of VEGF. VEGF/bioceramic chemical interactions were studied mainly by Raman imaging in order to follow the successive steps of the functionalisation by VEGF of the polished surface of ceramics made of hydroxyapatite (HA) and carbonated hydroxyapatite (CHA). This approach allowed to map the surface chemical changes and to point out the spatial distribution as well as the preferential reactions between the intermediate molecules and VEGF depending of the substrate.

No description available.