Unveiling the impact of the effective particles distribution on strengthening mechanisms: A multiscale characterization of Mg+Y2O3 nanocomposites

International audienceMost models used to account for the hardening of nanocomposites only consider a global volume fraction of particles which is a simplified indicator that overlooks the particles size and spatial distribution. The current study aims at quantifying the effect of the real experimental particles spatial and size distribution on the strengthening of a magnesium based nanocomposites reinforced with Y 2 O 3 particles processed by Friction Stir Processing (FSP). X-ray tomographic 3-D images allowed to identify the best FSP parameters for the optimum nanocomposite. A detailed analysis indicates that the observed hardening is mainly due to Orowan strengthening and the generation of geometrically necessary dislocations (GND) due to thermal expansion coefficients (CTE) mismatch between magnesium and Y 2 O 3 particles. A multiscale characterization coupling 3D X-ray laboratory, synchrotron nanoholotomography and transmission electron microscopy (TEM) has been used to investigate particles size and spatial distribution over four orders of magnitude in length scales. Two dedicated micromechanical models for the two strengthening mechanisms are applied on the experimental particle fields taking into account the real particles size and spatial distribution, and compared to classical models based on average data. This required to develop a micromechanical model for CTE mismatch hardening contribution. This analysis reveals that the contribution from CTE mismatch is decreased by a factor two when taking into account the real distribution of particles instead of an average volume fraction

Investigation of the human pineal gland 3D organization by X-ray phase contrast tomography

Pineal gland (PG) is a part of the human brain epithalamus that plays an important role in sleep, circadian rhythm, immunity, and reproduction. The calcium deposits and lesions in PG interfere with normal function of the organ and can be associated with different health disorders including serious neurological diseases. At the moment, the detailed mechanisms of PG calcifications and PG lesions formation as well as their involvement in pathological processes are not fully understood. The deep and comprehensive study of the structure of the uncut human PG with histological details, poses a stiff challenge to most imaging techniques, due to low spatial resolution, low visibility or to exceedingly aggressive sample preparation. Here, we investigate the whole uncut and unstained human post-mortem PGs by X-ray phase contrast tomography (XPCT). XPCT is an advanced 3D imaging technique, that permits to study of both soft and calcified tissue of a sample at different scales: from the whole organ to cell structure. In our research we simultaneously resolved 3D structure of parenchyma, vascular network and calcifications. Moreover, we distinguished structural details of intact and degenerated PG tissue. We discriminated calcifications with different structure, pinealocytes nuclei and the glial cells processes. All results were validated by histology. Our research clear demonstrated that XPCT is a potential tool for the high resolution 3D imaging of PG morphological features. This technique opens a new perspective to investigate PG dysfunction and understand the mechanisms of onset and progression of diseases involving the pineal gland

Illuminating the Brain With X-Rays: Contributions and Future Perspectives of High-Resolution Microtomography to Neuroscience

The assessment of three-dimensional (3D) brain cytoarchitecture at a cellular resolution remains a great challenge in the field of neuroscience and constant development of imaging techniques has become crucial, particularly when it comes to offering direct and clear obtention of data from macro to nano scales. Magnetic resonance imaging (MRI) and electron or optical microscopy, although valuable, still face some issues such as the lack of contrast and extensive sample preparation protocols. In this context, x-ray microtomography (μCT) has become a promising non-destructive tool for imaging a broad range of samples, from dense materials to soft biological specimens. It is a new supplemental method to be explored for deciphering the cytoarchitecture and connectivity of the brain. This review aims to bring together published works using x-ray μCT in neurobiology in order to discuss the achievements made so far and the future of this technique for neuroscience

Computational design of biopolymer aerogels and predictive modelling of their nanostructure and mechanical behaviour

To address the challenge of reconstructing or designing the three-dimensional microstructure of nanoporous materials, we develop a computational approach by combining the random closed packing of polydisperse spheres together with the Laguerre–Voronoi tessellation. Open-porous cellular network structures that adhere to the real pore-size distributions of the nanoporous materials are generated. As an example, κ-carrageenan aerogels are considered. The mechanical structure–property relationships are further explored by means of finite elements. Here we show that one can predict the macroscopic stress–strain curve of the bulk porous material if only the pore-size distributions, solid fractions, and Young’s modulus of the pore-wall fibres are known a priori. The objective of such reconstruction and predictive modelling is to reverse engineer the parameters of their synthesis process for tailored applications. Structural and mechanical property predictions of the proposed modelling approach are shown to be in good agreement with the available experimental data. The presented approach is free of parameter-fitting and is capable of generating dispersed Voronoi structures

Sample Preparation and Warping Accuracy for Correlative Multimodal Imaging in the Mouse Olfactory Bulb Using 2-Photon, Synchrotron X-Ray and Volume Electron Microscopy

Integrating physiology with structural insights of the same neuronal circuit provides a unique approach to understanding how the mammalian brain computes information. However, combining the techniques that provide both streams of data represents an experimental challenge. When studying glomerular column circuits in the mouse olfactory bulb, this approach involves e.g., recording the neuronal activity with in vivo 2-photon (2P) calcium imaging, retrieving the circuit structure with synchrotron X-ray computed tomography with propagation-based phase contrast (SXRT) and/or serial block-face scanning electron microscopy (SBEM) and correlating these datasets. Sample preparation and dataset correlation are two key bottlenecks in this correlative workflow. Here, we first quantify the occurrence of different artefacts when staining tissue slices with heavy metals to generate X-ray or electron contrast. We report improvements in the staining procedure, ultimately achieving perfect staining in ∼67% of the 0.6 mm thick olfactory bulb slices that were previously imaged in vivo with 2P. Secondly, we characterise the accuracy of the spatial correlation between functional and structural datasets. We demonstrate that direct, single-cell precise correlation between in vivo 2P and SXRT tissue volumes is possible and as reliable as correlating between 2P and SBEM. Altogether, these results pave the way for experiments that require retrieving physiology, circuit structure and synaptic signatures in targeted regions. These correlative function-structure studies will bring a more complete understanding of mammalian olfactory processing across spatial scales and time

X-ray and neutron μCT of biomedical samples: from image acquisition to quantification

Even though the validity of x-ray computed tomography in the analysis of biomedical samples is nowadays undisputed, the more recent imaging techniques and more advanced instruments (such as synchrotrons) are still relatively unknown to many medical doctors that could benefit from them.The doctoral work presented in this thesis joins a collective effort from the imaging community to demonstrate potential applications of advanced x-ray and neutron imaging methods to preclinical medical research, with the hope of contributing to reach a “critical mass” in the medical community and in the public opinion as well.Two main lines of work are detailed, one focused on the ex vivo evaluation of corrosion processes of magnesium-based biodegradable implants for osteosynthesis, the other dedicated to the assessment of neuropathy in human gastroenteric dysmotility. The aimed endpoint was to develop pipelines, from image acquisition all the way to data quantification, that could be used by other research groups with similar questions and may inspire future interdisciplinary collaborations between medicine, natural science and engineering.In the first line of work, we have attempted to employ synchrotron-radiation micro-computed tomography (µCT) coupled with in situ loading tests to assess the mechanical properties of the bone-implant interface (Paper I). We have revealed the crucial importance of the radiation dose deposited on the sample, and that the mechanical loading geometry should be accurately determined in the planning steps of the experiment. Moving away from the mechanical testing, we have also explored a novel three-dimensional analysis of the corrosion by-products of biodegradable implants by combining x-ray µCT, neutron µCT and x-ray fluorescence mapping (Papers IV and V). The second line of work has assessed the potential of x-ray phase-contrast µCT and nano-resolution holotomography as ways to perform virtual histology of unstained peripheral and autonomic neural tissue. In full-thickness biopsies of the myenteric nervous system, qualitative and potentially quantitative differences have been shown between controls and patients affected by gastrointestinal dysmotility (Paper II). In unstained skin biopsies, the methods have failed to visualise peripheral nerves, but we could identify structural changes in the connective tissue of some patients when compared to controls and other patients (Paper III)

A multi-scale imaging approach to understand osteoarthritis development

X-ray phase-contrast imaging is an innovative and advanced imaging method. Contrary to conventional radiology, where the image contrast is primarily determined by X-ray attenuation, phase-contrast images contain additional information generated by the phase shifts or refraction of the X-rays passing through matter. The refractive effect on tissue samples is orders of magnitude higher than the absorption effect in the X-ray energy range used in biomedical imaging. This technique makes it possible to produce excellent and enhanced image contrast, particularly when examining soft biological tissues or features with similar X-ray attenuation properties. In combination with high spatial resolution detector technology and computer tomography, X-ray phase-contrast imaging has been proved to be a powerful method to examine tissue morphology and the evolution of pathologies three-dimensionally, with great detail and without the need of contrast agents. This Thesis work has focused on developing an accurate, multi-scale X-ray-based methodology for imaging and characterizing the early stages of osteoarthritis. X-ray phase-contrast images acquired at different spatial resolutions provide unprecedented insights into cartilage and the development of its degeneration, i.e., osteoarthritis. Other types of X-ray phase-contrast imaging techniques and setups using spatial resolutions ranging from micrometer down to nanometer were applied. Lower spatial resolutions allow large sample coverage and comprehensive representations, while the nanoscale analysis provides a precise depiction of anatomical details and pathological signs. X-ray phase-contrast results are correlated to data obtained, on the same specimens, by standard laboratory methods, such as histology and transmission electron microscopy. Furthermore, X-ray phase-contrast images of cartilage were acquired using different X-ray sources and results were compared in terms of image quality. It was shown that with the use of synchrotron radiation, more detailed images and much faster data acquisitions could be achieved. A second focus in this Thesis work has been the investigation of the reaction of healthy and degenerated cartilage under different physical pressures, simulating the different levels of stress to which the tissue is subject during daily movements. A specifically designed setup was used to dynamically study cartilage response to varying pressures with X-ray phase-contrast micro-computed tomography, and a fully volumetric and quantitative methodology to accurately describe the tissue morphological variations. This study revealed changes in the behavior of the cartilage cell structure, which differ between normal and osteoarthritic cartilage tissues. The third focus of this Thesis is the realization of an automated evaluation procedure for the discrimination of healthy and cartilage images with osteoarthritis. In recent years, developments in neural networks have shown that they are excellently suited for image classification tasks. The transfer learning method was applied, in which a pre-trained neural network with cartilage images is further trained and then used for classification. This enables a fast, robust and automated grouping of images with pathological findings. A neural network constructed in this way could be used as a supporting instrument in pathology. X-ray phase-contrast imaging computed tomography can provide a powerful tool for a fully 3D, highly accurate and quantitative depiction and characterization of healthy and early stage-osteoarthritic cartilage, supporting the understanding of the development of osteoarthritis.Röntgen-Phasenkontrast-Bildgebung ist eine innovative und weiterführende Bildgebungsmethode. Im Gegensatz zu herkömlichen Absorptions-Röntgenaufnahmen, wie sie in der Radiologie verwendet werden, wird der Kontrast bei dieser Methode aus dem Effekt der Phasenverschiebung oder auch Brechung der Röngtenstrahlen gebildet. Der Brechungseffekt bei Gewebeproben ist um ein Vielfaches höher als der Absorptionseffekt des elektromagnetischen Spektrums der Röntgenstrahlen. Diese Methode ermöglicht die Darstellung von großen Kontraste im Gewebe. Unter Verwendung eines hochauflösenden Detektors und in Kombination mit der Computer-Tomographie, ist Phasenkontrast-Bildgebung eine sehr gute Methode um Knorpelgewebe und Arthrose im Knorpel zu untersuchen. Diese Arbeit beschreibt primär ein Verfahren zur Darstellung arthrotischen Knorpels im Anfangsstadium. Die mit verschiedenen Auflösungen und 3D-Phasen-Kontrast-Methoden produzierten Aufnahmen ermöglichen einen noch nie dagewesenen Einblick in den Knorpel und die Entwicklung von Arthrose im Anfangsstadium. Hierbei kam die propagationsbasierte Phasenkontrastmethode mit einer Auflösung im mikrometer Bereich und die (Nano)-Holotomographie-Methode mit einer Auflösung im Submicrometer Bereich zum Einsatz. Durch Auflösung im mikrometer Bereich kann ein großes Volumen im Knorpel gescannt werden, während die Nano-Holotomographie Methode eine sehr große Detailauflösung aufweißt. Die Phasenkontrast-Aufnahmen werden mit zwei anderen wissenschaftlichen Methoden verglichen: mikroskopische Abbildungen histologisch aufgearbeiteter Knorpelproben und Aufnahmen eines Transmissionselektroskop zeigen sehr große Übereinstimmungen zur Röntgen-Phasenkontrast-Bildgebung. Desweiteren wurden Phasenkontrast-Aufnahmen von Knorpel aus unterschiedlichen Röntgenquellen verglichen. Hierbei zeigte sich, dass mit Hilfe des Teilchenbeschleunigers (Synchrotron) detailreichere und schnellere Aufnahmen erzielt werden können. Bilder aus Flüssig-Metall-Quellen zeigen sich durchaus von guter Qualität, erfordern jedoch sehr lange Aufnahmezeiten. In dieser Arbeit wird zudem das Verhalten von Knorpelgewebe, welches ein Anfangsstadium von Arthrose aufweist, unter physikalischem Druck untersucht. Hierfür wurden 3D-Computertomographie-Aufnahmen von komprimiertem Knorpelgewebe angefertig und mit Aufnahmen ohne Komprimierung verglichen. Ein quantitativer Vergleich machte Veränderungen des Verhaltens der Knorpelzellstruktur (Chondronen) sichtbar. Es konnte gezeigt werden, dass Chondrone bei arthrotischem Knorpel ein verändertes Kompressionsverhalten haben. Der dritte Fokus dieser Arbeit liegt auf der automatisierten Auswertung von Aufnahmen gesunden und arthrotischen Knorpelgewebes. Die Entwicklungen im Bereich der Neuronale Netze zeigten in den letzten Jahren, dass diese sich hervoragend für Bildklassifizierungsaufgaben eignen. Es wurde die Methode des transferierenden Lernens angewandt, bei der ein vortrainiertes Neuronales Netz mit Knorpelbildern weitertrainiert und anschließend zur Klassifizierung eingesetzt wird. Dadurch ist eine schnelle, robuste und automatisierte Gruppierung von Bildern mit pathologischen Befunden möglich. Ein derart konstruiertes Neuronales Netz könnte als unterstützendes Instrument in der Pathologie angewandt werden. Röntgen-Phasenkontrast-CT kann ein leistungsstarkes Werkzeug für eine umfassende, hochpräzise und quantitative 3D-Darstellung und Charakterisierung von gesundem Knorpel und athrotischem Knorpel im Frühstadium bieten, um das Verständnis der Entwicklung von Osteoarthritis zu erweitern

A multi-technique hierarchical X-ray phase-based approach for the characterization and quantification of the effects of novel radiotherapies

Cancer is the first or second leading cause of premature deaths worldwide with an overall rapidly growing burden. Standard cancer therapies include surgery, chemotherapy and radiotherapy (RT) and often a combination of the three is applied to improve the probability of tumour control. Standard therapy protocols have been established for many types of cancers and new approaches are under study especially for treating radio-resistant tumours associated to an overall poor prognosis, as for brain and lung cancers. Follow up techniques able to monitor and investigate the effects of therapies are important for surveying the efficacy of conventionally applied treatments and are key for accessing the curing capabilities and the onset of acute and late adverse effects of new therapies. In this framework, this doctoral Thesis proposes the X-ray Phase Contrast Im-aging - Computed Tomography (XPCI-CT) technique as an imaging-based tool to study and quantify the effects of novel RTs, namely Microbeam and Minibeam Radiation therapy (MRT and MB), and to compare them to the standard Broad Beam (BB) induced effects on brain and lungs. MRT and MB are novel radiotherapies that deliver an array of spatially fractionated X-ray beamlets issued from a synchrotron radiation source, with widths of tens or hundreds of micrometres, respectively. MRT and MB exploit the so-called dose-volume effect: hundreds of Grays are well tolerated by healthy tissues and show a preferential effect on tumour cells and vasculature when delivered in a micrometric sized micro-plane, while induce lethal effects if applied over larger uniform irradiation fields. Such highly collimated X-ray beams need a high-resolution and a full-organ approach that can visualize, with high sensitivity, the effects of the treatment along and outside the beamlets path. XPCI-CT is here suggested and proven as a powerful imaging technique able to determine and quantify the effects of the radiation on normal and tumour-bearing tissues. Moreover, it is shown as an effective technique to complement, with 3D information, the histology findings in the follow-up of the RT treatments. Using a multi-scale and multi-technique X-ray-based approach, I have visualized and analysed the effects of RT delivery on healthy and glioblastoma multiforme (GBM)-bearing rat brains as well as on healthy rat lungs. Ex-vivo XPCI-CT datasets acquired with isotropic voxel sizes in the range 3.253 – 0.653 μm3 could distinguish, with high sensitivity, the idiopathic effects of MRT, MB and BB therapies. Histology, immunohistochemistry, Small- and Wide-Angle X-ray Scattering and X-ray Fluorescence experiments were also carried out to accurately interpret and complement the XPCI-CT findings as well as to obtain a detailed structural and chemical characterization of the detected pathological features. Overall, this multi-technique approach could detect: i) a different radio-sensitivity for the MRT-treated brain areas; ii) Ca and Fe deposits, hydroxyapatite crystals formation; iii) extended and isolated fibrotic contents. Full-organ XPCI-CT datasets allowed for the quantification of tumour and mi-crocalcifications’ volumes in treated brains and the amount of scarring tissue in irradiated lungs. Herein, the role of XPCI-CT as a 3D virtual histology technique for the follow-up of ex-vivo RT effects has been assessed as a complementary method for an accurate volumetric investigation of normal and pathological states in brains and lungs, in a small animal model. Moreover, the technique is proposed as a guidance and auxiliary tool for conventional histology, which is the gold standard for pathological evaluations, owing to its 3D capabilities and the possibility of virtually navigating within samples. This puts a landmark for XPCI-CT inclusion in the pre-clinical studies pipeline and for advancing towards in-vivo XPCI-CT imaging of treated organs.Weltweit gilt Krebs als häufigste bzw. zweithäufigste Ursache eines zu früh erfolgenden Todes, wobei die Zahlen rasch ansteigen. Standardmäßige Krebstherapien umfassen chirurgische Eingriffe, Chemotherapie und Strahlentherapie (radiotherapy, RT); oft kommt eine Kombination daraus zur Anwendung, um die Wahrscheinlichkeit der Tumorkontrolle zu erhöhen. Es wurden Standardtherapieprotokolle für zahlreiche Krebsarten eingerichtet und es wird vor allem in der Behandlung von strahlenresistenten Tumoren mit allgemein schlechter Prognose wie bei Hirn- und Lungentumoren an neuen Ansätzen geforscht. Nachverfolgungstechniken, welche die Auswirkungen von Therapien überwachen und ermitteln, sind zur Überwachung der Wirksamkeit herkömmlich angewandter Behandlungen wichtig und auch maßgeblich am Zugang zu den Fähigkeiten zur Heilung sowie zum Auftreten akuter und verzögerter Nebenwirkungen neuer Therapien beteiligt. In diesem Rahmenwerk unterbreitet diese Doktorarbeit die Technik der Röntgen-Phasenkontrast-Bildgebung über Computertomographie (X-ray Phase Contrast Imaging - Computed Tomography, XPCI‑CT) als bildverarbeitungs-basiertes Tool zur Untersuchung und Quantifizierung der Auswirkungen neuartiger Strahlentherapien, nämlich der Mikrobeam- und Minibeam-Strahlentherapie (MRT und MB), sowie zum Vergleich derselben mit den herkömmlichen durch Breitstrahlen (Broad Beam, BB) erzielten Auswirkungen auf Gehirn und Lunge. MRT und MB sind neuartige Strahlentherapien, die ein Array räumlich aufgeteilter Röntgenstrahlenbeamlets aus einer synchrotronen Strahlenquelle mit einer Breite von Zehnteln bzw. Hundersteln Mikrometern abgeben. MRT und MB nutzen den sogenannten Dosis-Volumen-Effekt: Hunderte Gray werden von gesundem Gewebe gut vertragen und wirken bei der Abgabe in einer Mikroebene im Mikrometerbereich vorrangig auf Tumorzellen und Blutgefäße, während sie bei einer Anwendung über größere gleichförmige Strahlungsfelder letale Auswirkungen aufweisen. Solche hoch kollimierten Röntgenstrahlen erfordern eine hohe Auflösung und einen Zugang zum gesamten Organ, bei dem die Auswirkungen der Behandlung entlang und außerhalb der Beamletpfade mit hoher Empfindlichkeit visualisiert werden können. Hier empfiehlt und bewährt sich die XPCI‑CT als leistungsstarke Bildverarbeitungstechnik, welche die Auswirkungen der Strahlung auf normale und tumortragende Gewebe feststellen und quantifizieren kann. Außerdem hat sich gezeigt, dass sie durch 3‑D-Informationen eine effektive Technik zur Ergänzung der histologischen Erkenntnisse in der Nachverfolgung der Strahlenbehandlung ist. Anhand eines mehrstufigen und multitechnischen röntgenbasierten Ansatzes habe ich die Auswirkungen der Strahlentherapie auf gesunde und von Glioblastomen (GBM) befallene Rattenhirne sowie auf gesunde Rattenlungen visualisiert und analysiert. Mit isotropen Voxelgrößen im Bereich von 3,53 bis 0,653 μm3 erfasste Ex-vivo-XPCI-CT-Datensätze konnten die idiopathischen Auswirkungen der MRT-, MB- und BB‑Behandlung mit hoher Empfindlichkeit unterscheiden. Es wurden auch Experimente zu Histologie, Immunhistochemie, Röntgenklein- und ‑weitwinkelstreuung und Röntgenfluoreszenz durchgeführt, um die XPCI‑CT-Erkenntnisse präzise zu interpretieren und zu ergänzen sowie eine detaillierte strukturelle und chemische Charakterisierung der nachgewiesenen pathologischen Merkmale zu erhalten. Im Allgemeinen wurde durch diesen multitechnischen Ansatz Folgendes ermittelt: i) eine un-terschiedliche Strahlenempfindlichkeit der mit MRT behandelten Gehirnbereiche; ii) Ca- und Fe-Ablagerungen und die Bildung von Hydroxylapatitkristallen; iii) ein ausgedehnter und isolierter Fibrosegehalt. XPCI‑CT-Datensätze des gesamten Organs ermöglichten die Quantifizierung der Volume von Tumoren und Mikroverkalkungen in den behandelten Gehirnen und der Menge des Narbengewebes in bestrahlten Lungen. Dabei wurde die Rolle der XPCI‑CT als virtuelle 3‑D-Histologietechnik für die Nachverfolgung von Ex-vivo-RT‑Auswirkungen als ergänzende Methode für eine präzise volumetrische Untersuchung des normalen und pathologischen Zustands von Gehirnen und Lungen im Kleintiermodell untersucht. Darüber hinaus wird die Technik aufgrund ihrer 3‑D-Fähigkeiten und der Möglichkeit zur virtuellen Navigation in den Proben als Leitfaden und Hilfstool für die herkömmliche Histologie vorgeschlagen, die der Goldstandard für die pathologische Evaluierung ist. Dies markiert einen Meilenstein für die Übernahme der XPCI‑CT in die Pipeline präklinischer Studien und für den Übergang zur In-vivo-XPCI‑CT von behandelten Organen

Synthesis, characterization and structure-properties relationship of aerogels and aerogel-based composites

During the last few years, cellular materials research has pointed to aerogels as one of the most promising materials. This is due to the combination of properties, such as their low density, large specific surface area, excellent thermal and acoustic insulation, and high porosity. These properties are the consequence of their interesting structures characterized by pores and particles in the nanometric scale. This thesis focuses on the synthesis and characterization of aerogels and aerogel-based composites. The main objective has been the development of polyurethane-based organic aerogels obtained by sol-gel technology followed by supercritical drying. These materials present interesting optical properties (transparency to visible light), a thermal conductivity below that of the aerogels previously described for this matrix (included in the superinsulating range), achieving values of 12 mW/mK, and superior mechanical properties than the widely investigated silica aerogels. Additionally, the effect of the addition of infrared blockers on its thermal conductivity has been studied. On the other hand, the incorporation of polyurethane foams with reticulated structures during the synthesis of silica aerogels has allowed the notable improvement of their mechanical properties, providing them with great stiffness and flexibility. In addition, these materials have excellent thermal insulation. As a result of this research, the relationship between formulation-process-structure-properties has been understood, so that, through the analysis of different parameters, their influence on the final properties has been identified. Thus, certain synthesis strategies are established allowing to obtain promising aerogels with potential application in the construction, automotive, and aeronautics sectors, among others. This thesis, supervised by Prof. Dr. Miguel Ángel Rodríguez-Pérez and Prof. Dr. Fernando Villafañe González, constitutes the opening of a new research line at CellMat Laboratory, Department of Condensed Matter Physics of the University of Valladolid, allowing the development of numerous lines of future work.Durante los últimos años, la investigación en campo de los materiales celulares ha señalado a los aerogeles como uno de los materiales más prometedores. Esto es debido a la combinación de propiedades entre las cuales se encuentran su baja densidad, gran superficie específica, excelente aislamiento térmico y acústico, y alta porosidad. Estas propiedades son la consecuencia directa de sus interesantes estructuras caracterizadas por tamaños de poro y partículas que se encuentran en la escala nanométrica. Esta tesis se centra en la síntesis y caracterización de aerogeles y materiales compuestos basados en aerogel. El principal objetivo ha sido el desarrollo de aerogeles orgánicos en base poliuretano obtenidos mediante la tecnología sol-gel seguida de secado supercrítico. Estos materiales presentan propiedades ópticas de interés (transparencia a la luz visible), una conductividad térmica por debajo de los aerogeles previamente descritos para esta matriz, que están comprendidos en el rango del superaislamiento consiguiendo valores de tan solo 12 mW/mK, y unas propiedades mecánicas superiores a los aerogeles de sílice ampliamente investigados. Adicionalmente, se ha estudiado el efecto de la adición de partículas bloqueadoras de la radiación infrarroja en su conductividad térmica. Por otro lado, la incorporación de espumas de poliuretano con estructuras reticuladas durante la síntesis de aerogeles de sílice ha permitido la notable mejora de sus propiedades mecánicas, proporcionándoles una gran resistencia a la compresión y flexibilidad. Además, estos materiales presentan un aislamiento térmico excelente. Como resultado de esta investigación, se ha comprendido la relación entre formulación- proceso-estructura propiedades, de forma que, mediante el análisis de diferentes parámetros, se ha identificado su influencia en las propiedades finales. Así, se establecen ciertas estrategias de síntesis que permiten la obtención de aerogeles prometedores con potencial aplicación en el sector de la construcción, automoción, aeronáutica, entre otros. Esta tesis, supervisada por el Prof. Dr. Miguel Ángel Rodríguez-Pérez el Prof. Dr. Fernando Villafañe González, constituye la apertura de una nueva línea de investigación en el Laboratorio CellMat del Departamento de Física de la Materia Condensada de la Universidad de Valladolid, permitiendo el desarrollo de numerosas líneas de trabajo futuro.Escuela de DoctoradoDoctorado en Físic