[EN] The development of new and more complex polymeric materials involves challenging problems to basic sciences. The relationship between structure and molecular dynamics assumes great importance for the future development of novel technologies based on such polymers. Thus, the understanding of how small changes in the chemical structure affect the properties of the material is essential to progress in the technological and scientific area. An in-depth analysis of the molecular mobility leads to establish the structure-properties relationships. On this basis, the main aim of the present work is to study the molecular mobility of two different families of polymeric materials. For this purpose, the experimental techniques mainly used were Differential Scanning Calorimetry (DSC) and Dielectric Relaxation Spectroscopy (DRS). The first family of polymers characterized was a series of chemically cross-linked copolymers composed by Vinylpyrrolidone (VP) and Butyl Acrylate (BA) monomers. In the first place, the influence of the monomer molar ratio (XVP/YBA) on the copolymer properties was studied. Thus, a Fourier Transform Infrared Spectroscopy (FTIR) analysis verified dipole-dipole interactions between amide groups. The influence of these interactions on several parameters related to the molecular mobility was evidenced by the DSC, DRS and Dynamic Mechanical Analysis (DMA) techniques. Secondly, the effect of the cross-link density on the molecular dynamics of 60VP/40BA copolymers was analyzed using DSC and DRS. One single glass transition was detected by DSC measurements. The DRS analysis showed that an increase of the cross-linking produced a typical effect on the alpha process dynamics. However, the beta process, which possessed typical features of pure JG relaxation, unexpectedly lost the intermolecular character for the highest cross-linker content. The fastest gamma process was relatively unaffected. The second family of polymeric materials studied was a series of segmented polycarbonatediol polyurethane (PUPH) modified with different amounts of expanded graphite (EG) conductive filler. Scanning Electron Microscopy (SEM), X-ray diffraction measurements and FTIR analysis demonstrated a homogeneous dispersion of the EG filler in the matrix. DRS was used to study the dielectric properties of the PUPH/EG composites. The dielectric permittivity of the composites showed an insulator to conductor percolation transition with the increase of the EG content (2030 wt%). The addition of expanded graphite to the matrix caused a dramatic increase in the electrical conductivity of ten orders of magnitude, which is an indication of percolative behavior. / [ES] El desarrollo de nuevos materiales poliméricos de mayor complejidad produce un desafío cada vez mayor en el área de las ciencias básicas. La relación entre la estructura y la dinámica molecular resulta de gran importancia para el desarrollo de nuevas tecnologías basadas en estos materiales poliméricos. Así, una mayor comprensión de cómo pequeños cambios en la estructura química afectan a las propiedades de los materiales resulta esencial para el progreso científico y tecnológico. Un análisis en profundidad de la movilidad molecular permite establecer las relaciones estructura-propiedades. Partiendo de esta base, el principal objetivo del presente trabajo es el estudio de la movilidad molecular de dos familias diferentes de materiales poliméricos. Para ello, las técnicas experimentales utilizadas fueron principalmente la Calorimetría Diferencial de Barrido (DSC) y la Espectroscopia de Relajación Dieléctrica (DRS). La primera familia de polímeros caracterizada fue una serie de copolímeros entrecruzados químicamente compuestos por los monómeros Vinilpirrolidona (VP) y Acrilato de Butilo (BA). En primer lugar, se estudió la influencia de la proporción molar de monómero (XVP/YBA) en las propiedades del copolímero. A través de un análisis por Espectroscopia de Infrarrojo por Transformada de Fourier (FTIR), se verificó la existencia de interacciones dipolo-dipolo entre los grupos amida. Mediante el análisis por DSC, DRS y Análisis Dinamomecánico (DMA), se evidenció la influencia de estas interacciones en diferentes parámetros relacionados con la movilidad molecular. En segundo lugar, se analizó el efecto de la densidad de entrecruzamiento en la dinámica molecular de los copolímeros 60VP/40BA usando DSC y DRS. A través de las medidas de DSC se observó una única transición vítrea para todos los entrecruzamientos. El análisis por DRS mostró como el incremento en entrecruzante produjo el típico efecto en la dinámica del proceso alpha, pero sin embargo, el proceso beta, que tenía las características típicas de una relajación JG, perdió de forma inesperada su carácter intermolecular para el mayor contenido en entrecruzante. El proceso gamma no se vio afectado. La segunda familia de materiales poliméricos estudiada fue una serie de poliuretanos segmentados (PUPH) modificados con diferentes cantidades de grafito expandido (EG), utilizado como relleno conductivo (desde 0 a 50% en peso). El análisis de los resultados obtenidos mediante Microscopía Electrónica de Barrido (SEM), Difracción de Rayos X y FTIR demostró la homogénea dispersión del relleno de EG en la matriz de PUPH. La técnica DRS se usó para estudiar las propiedades dieléctricas de los materiales compuestos PUPH/EG. La permitividad dieléctrica de los materiales mostró una transición de percolación desde aislante a conductor al incrementarse el contenido en EG (rango de 20-30% en peso). La adición de grafito expandido a la matriz de PUPH causó un incremento significativo en la conductividad dieléctrica de diez órdenes de magnitud, lo que indica el comportamiento de percolación. / [CAT] El desenvolupament de nous materials polimèrics de major complexitat produeix un desafiament cada vegada major en l'àrea de les ciències bàsiques. La relació entre l'estructura i la dinàmica molecular resulta de gran importància per al desenrotllament de noves tecnologies basades en aquests materials polimèrics. Així, una major comprensió de com petits canvis en l'estructura química afecten a les propietats dels materials, resulta essencial per al progrés científic i tecnològic. Un anàlisis en profunditat de la mobilitat molecular permet establir les relacions estructura-propietats. Partint d'aquesta base, el principal objectiu del present treball és l'estudi de la mobilitat molecular de dues famílies diferents de materials polimèrics. Per a això, les tècniques experimentals utilitzades van ser principalment la Calorimetria Diferencial de Rastreig (DSC) i l'Espectroscòpia de Relaxació Dielèctrica (DRS). La primera família de polímers caracteritzada va ser una sèrie de copolímers entrecreuats químicament compostos pels monòmers Vinilpirrolidona (VP) i Acrilat de Butilo (BA) . En primer lloc, es va estudiar la influència de la proporció molar de monòmer (XVP/YBA) en les propietats del copolímer. A través d'una anàlisi per Espectroscòpia d'Infraroig per Transformada de Fourier (FTIR), es va verificar l'existència d'interaccions dipol-dipol entre els grups amida. Mitjançant l'anàlisi per DSC, DRS i Anàlisi Dinamomecánico (DMA), es va evidenciar la influència d'aquestes interaccions en diferents paràmetres relacionats amb la mobilitat molecular. En segon lloc, es va analitzar l'efecte de la densitat d'entrecreuament en la dinàmica molecular dels copolímers 60VP/40BA mitjançant DSC i DRS. A través de les mesures de DSC es va observar una única transició vítria per a tots els continguts d'agent entrecreuant . L'anàlisi per DRS va mostrar com l'increment en agent entrecreuant va produir l'efecte esperat en la dinàmica del procés alfa. En canvi, el procés beta, que tenia les característiques típiques d'una relaxació JG, va perdre de forma inesperada el seu caràcter intermolecular per al major contingut en agent entrecreuant. El procés més ràpid gamma no es va veure afectat. La segona família de materials polimèrics estudiada va ser una sèrie de poliuretans segmentats (PUPH) modificats amb diferents quantitats de grafit expandit (EG) , utilitzat com a farcit conductiu (des de 0 a 50% en pes). L'anàlisi dels resultats obtinguts per mitjà de Microscòpia Electrònica de Rastreig (SEM), Difracció de Rajos X i FTIR va mostrar la dispersió homogènia del EG en la matriu de PUPH. La tècnica DRS es va utilitzar per a estudiar les propietats dielèctriques dels materials compostos PUPH/EG. La permitivitat dielèctrica dels materials va mostrar una transició de percolació des d'aïllant a conductor amb l'increment de contingut en EG (20-30% en pes). L'addició d'EG a la matriu de PUPH va causar un increment significatiu en la conductivitat dielèctrica, de deu ordes de magnitud. / Redondo Foj, MB. (2015). A contribution to the study of the molecular mobility in polymeric materials by Thermal and Dielectric Analysis [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/59457 / TESIS

Study of Production Drifts Stability and Assessment of Reinforcement Requirements at LKAB Konsuln Test-Mine Levels 436 and 486 Using Geologic Structures Data, and Modelling Software - Dips and Unwedge:  a Part of dp1 Project (Mine Layout and Technology) of the Sustainable Underground Mining (Sum) Project Oludare Joseph Olufe Global population has been on exponential increase over the past half century. The population explosion is driving massive urbanization and infrastructure developments across the globe, which result in huge demand for metals, especially steel. The trend is forecasted to continue to rise steeply in for the next two decades. This is putting enormous strain on metals mining, especially because new surface economic deposits are rare to come by. Therefore, mining is steadily going deeper in many of the mining destinations across the world.     Mining at great depths present unique challenges, particularly regarding stability of excavations at depths. Rock falls, rock burst, excavation collapse are common occurrences associated with deep mining. In regions with high seismicity potentials the frequency and consequences could be very high. Over the past decade ground instability has become a significant challenge confronting mining at LKAB deep mines. There had been incidents that resulted in long term closure of sections of the mines, with resultant adverse economic impacts. More undesirable is loss of live of personnel.     The study was conducted at the Konsuln test mine levels 436 and 486, aimed to investigate the impacts of geologic structures on excavations instability at depths, at the Kiruna iron ore mines, on one hand.  And on the other hand, evaluate the influence of geologic structures on ground reinforcements at the mine. Structural data were collected and analysed using Dips program to define orientation of major structures. The results were used for wedge analysis and excavations stability modelling using Unwedge program. Important rock mechanical parameters were defined based on data provided, and others based on literatures. A design factor of safety of 1.5 was used.     Results from the study established that structures have significant impact on excavations instability at the Konsuln mine. 100% of the production drifts studied has minimum of four wedges formed in its perimeters. Out of this approximately 37% has factor of safety lower than 1.5. Evaluation of reinforcements (shotcrete and rock bolts) implemented in the mine found that approximately 15% of the total wedges formed in the production drifts has factor of safety less that 1.5 after both shotcrete and rock bolt reinforcements had been implement. Also, approximately 5% of the total wedges has apex height longer the rock bolt length.     It was therefore concluded that structurally induced instability is a major contributor to excavations instability at the Kiruna mine. The study approach presented a new methodology to understand and provide robust solution to ground instability problem at the mine.

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Design of braking system for the formula student car. Calculation of basic forces acting in the braking system, including the design of hydraulic circuits. Mechanical analysis of the most important parts of the braking system and pedal assembly. Thermal analysis of the brake discs. Manufacturing and total cost calculation.

Design of braking system for the formula student car. Calculation of basic forces acting in the braking system. Mechanical analysis of the most important parts of the braking system. Manufacturing of brake pedal. Assembly brake components to brake system.

Wood is a widely used construction material that has many advantageous properties, and some drawbacks. These drawbacks are mainly associated with the porous vascular structure of wood that makes it a high water-absorbent material. In addition, wood’s properties alter substantially with respect to the moisture content. Amongst the treatment techniques that limit the water uptake capacity of wood, vacuum-aided impregnation has exhibited promising results. However, little research has explored the effect of key parameters (such as the vacuum pressure) on the effectiveness of the impregnation. This study aims to optimize the performance of SiO2 impregnation of spruce wood under vacuum pressures. The main objective of this research is to overcome wood’s weakness by reducing its water uptake capacity through a vacuum-aided impregnation technique and study its effect on the physico-mechanical properties of wood under dry and saturated conditions. The study was conducted in two parts. In the first part, wood samples underwent impregnation under atmospheric and three vacuum pressures. Density measurements, water uptake tests, microscopy examination, thermogravimetric analysis, and dynamic mechanical analysis were conducted on non-treated and SiO2-treated samples. Quantitative and qualitative analyses demonstrated that SiO2 impregnation performed under -90 kPa was able to effectively enhance the wood’s properties compared to the other conditions. The SiO2 impregnation under high vacuum pressure demonstrated an effective increase in the density of the wood and achieved a significant reduction in the water uptake capacity. The analysis of the wood’s viscoelastic properties revealed that SiO2 impregnation under atmospheric and vacuum conditions triggered two different reinforcing mechanisms: a solid film, causing stick-slip oscillation, and particle diffusion, causing particle-particle and particle-lumen wall friction, respectively. For the second part, characterization methods such as Impact test, DMA, SEM, EDS, Porosity, and SAXS tests were conducted on non-treated and -90 kPa treated spruce wood samples in dry, saturated, and submerged states in order to reveal the synergistic effect of the SiO2 impregnation pressure and water uptake on the wood’s properties. The results showed that high vacuum impregnation pressure has a significant positive reinforcing effect on the wood’s properties. It increased the impact resistance of wood in dry and saturated conditions. A high vacuum impregnation was able to overcome the softening effect of water and caused a significant increase in the Storage modulus by strengthening the wood’s vascular structure, which accordingly increased the wood’s capacity to absorb energy. High vacuum impregnation was also able to counteract the plasticizing effect of water and significantly increased the Loss modulus by increasing the internal friction in the wood with the diffusion of the nanoparticles in the wood’s cell walls and vascular structure. This phenomenon increased the wood's capacity to absorb and dissipate energy under dry and submerged conditions.

New resin-based composites and resin-infiltrated ceramics are used to fabricate computer-aided design (CAD) and computer-aided manufacturing (CAM)-based restorations, although little information is available on the long-term performance of these materials. The aim of this investigation was to determine the effects of storage time (24 h, 90 days, 180 days) on the thermophysical properties of resin-based CAD/CAM materials. Thermogravimetric Analysis (TGA), differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) were used in the study. TGA provided insight into the composition of the resin-based materials and the influence of internal plasticization and water sorption. Resin-based composites showed different decomposition, heat energy and mechanical behavior, which was influenced by storage time in water. Individual materials such as Grandio bloc showed lower influence of water storage while maintaining good mechanical properties.

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