Functionally graded polymer nanocomposites using magnetic fields

Functionally Graded Materials (FGM) are a class of materials in which the composition and the properties gradually change over the volume. The present PhD project aims to generate a full understanding of a novel synthetic strategy for polymeric FGMs based on the magnetophoretic motion of magnetic nanofillers in a polymer matrix under the application of an external magnetic field gradient. Due to its high rate, costâeffectiveness and lowâtoxicity, UV polymerization was considered as the first curing option for the magnetic nanocomposites. The curability problem deriving from the presence of opaque particles was tackled by studying two different systems based on the same hyperbranched acrylated polymer matrix (HBP): one containing bare Fe3O4 nanoparticles whereas the other loaded with Fe3O4@SiO2 coreâshell nanoparticles. The employment of Fe3O4@SiO2 NPs for the synthesis of magnetic polymeric films showed to be effective towards the inclusion of 10âtimes higher particle volume fractions compared to formulations including bare Fe3O4. By adding Fe3O4@SiO2 nanoparticles to the UVâcurable matrix, the motion of the magnetic responsive filler was induced upon the application of magnetic field gradients generated by permanent magnets. The process was speeded up through the employment of a simple setâup composed of two block magnets in repulsion configuration and through the functionalization of the particle surfaces with an acrylated silane. From the experimental analysis of the photocuring process, the residual stresses arising during the photopolymerization of functionally graded composite coatings based on the UVâcurable HBP matrix and Fe3O4@SiO2 nanoparticles were evaluated with a Finite Element Method approach. These coatings were able to consistently decrease the residual stresses at the coatingâsubstrate interface compared to those encountered either in composites with homogeneous compositions or in the pure polymer, provided that reinforcing fillers were concentrated at the coatingâsubstrate interface. If instead nanoparticles were concentrated at the free surface, graded nanocomposite coatings could reduce by as much as 40% the interfacial stress arising from thermal variations, as demonstrated through numerical simulations. Nanoindentation tests were carried out on the surface of polymer nanocomposites exhibiting either graded or homogeneous distributions of Fe3O4@SiO2 nanoparticles in the UVâcurable matrix. It was experimentally shown how only at relatively small indentation depths, large increases in modulus and hardnesswere obtained for graded composites with respect to their homogeneous counterparts. Through a Material Point Method approach, experimental nanoindentation tests were successfully simulated. Finally, nanocomposite systems based on epoxy matrices were considered. In particular, composites with gradients in permittivity were synthesized through the application of a magnetic field to suspensions of highâpermittivity Fe3O4@TiO2 particles in an epoxy resin. The application of the magnetic force not only induced the movement of the particles, but also caused their alignment in high aspect ratio structures, resulting in rather steep permittivity gradients. Numerical simulations clarified how the asâsynthesized materials, employed as insulators, have the potential to efficiently reduce the electric field stress at the electrodeâinsulator interface and have intrinsic durability advantages over their homogeneous counterparts.

Low-Stress UV-Curable Hyperbranched Polymer Nanocomposites for High-Precision Devices

Valérie Geiser

The aim of this thesis was to investigate the process-structure-property relationships of UV-curable hyperbranched polymer (HBP)/silica nanocomposites. Special attention was paid to the interplay between photo-conversion, rheological behavior, shrinkage, and stress dynamics. This knowledge was used to maximize the shape fidelity and dimensional stability of imprinted nano-patterns made with these nanocomposites. Two different processing routes, resulting in different nanocomposite morphologies, were compared. The first and more conventional approach was ultrasonic, solvent-assisted mixing with solid silica nanoparticles followed by UV curing, which led to a discrete dispersion of silica particles in the matrix. The second and more novel approach was a dual-cure process combining UV and sol-gel processing with liquid tetraethyl orthosilicate. The sol-gel process, using a low-viscosity organometallic precursor, overcame the potential processing issue of the highly viscous particulate nanocomposites and led to a hybrid material with a homogeneous silica network at nanometer scale. Rheological analysis of silica nanoparticle suspensions up to the concentrated regime in the HBP showed an exponential increase of the viscosity with the particle fraction for well-dispersed discrete particle systems. A liquid-to-solid transition occurred in the 5 to 10 vol% range, which was correlated with an immobilized layer of polymer hydrogen-bonded to the silanol groups on the surface of the particles, as was confirmed by calorimetric analysis. Polymerization kinetics of HBP nanocomposites and hybrids were analyzed by means of photo differential scanning calorimetry using an autocatalytic model. A time-intensity-superposition principle with power-law dependence was established, which invalidated the classic radiation dose equivalence principle. Gelation and modulus build-up were monitored using photo-rheology. The calorimetric and rheological data were combined in the form of time-intensity-transformation diagrams. It was found that gelation was delayed with respect to conversion up to 36% when lower UV intensities were used, which favored reduce polymerization stresses. The dynamics of polymerization shrinkage and internal stress build-up were investigated using photo-hyphenated interferometry and beam-bending methods. The linear shrinkage of the HBP was as low as 4.5%, which was further reduced to 3.3% with the addition of 20 vol% nanoparticles. The residual stress of HBP/SiO2 nanocomposites was below 5.5 MPa. That is well below the level of standard non-reinforced resins, in spite of an increased stiffness. For the sol-gel hybrids with 20 vol% SiO2, stress reduction by 50% with simultaneous stiffness increase by 20% with respect to corresponding particulate composites was demonstrated. The coefficient of thermal expansion was also lowered by 30%. Finally, nanogratings with a period of 360 nm and a step height of 12 nm were fabricated using UV-nanoimprint lithography with a glass or nickel master in a low-pressure (max. 6 bar) and rapid (≈1 min) process. Stable gratings were imprinted in the composite material containing up to 25 vol% of silica nanoparticles, despite the high viscosity of such compositions. Thanks to the exudation of a HBP-rich surface layer, the shape fidelity in terms of period of the replicated patterns was within 98% of the master, with shape distortion increasing with internal stress. The obtained nanogratings were used as a substrate for grated high refractive index TiO2 waveguides and then applied as wavelength-interrogated optical sensors (WIOS). An immunoassay with the polymer WIOS showed the same ultrahigh detection sensitivity as the standard glass-based devices. Therefore, the novel polymer-based sensor should be useful to probe contaminants in liquids with concentrations as low as a few ppb.

EPFL2010

Tailored Capsule Based Self-Healing for Epoxy Matrix Composites

Sam Neuser

Self-healing materials are a novel class of materials able to repair structural or, more generally, functional damage to a part. They hence have the potential to improve reliability and cost effectiveness, because failure or loss of functionality may be postponed or completely avoided. This concept has been applied to all classes of materials, but is particularly suited to polymers and their composites. Indeed, it was first demonstrated for epoxies containing capsules of dicyclopentadiene and dispersed Grubbs’ catalyst. However, the high cost of the catalyst precludes commercial use of this self-healing system. In the present thesis, two alternative approaches to self-healing of an epoxy matrix were investigated: (1) a solvent based self-healing epoxy; (2) a two-component epoxy/amine self-healing system using a novel encapsulation technique. The solvent-based system showed efficient healing in an under-cured epoxy matrix. The solvent in question was ethyl phenylacetate (EPA) encapsulated with urea-formaldehyde (UF) or UF-polyurethane. It was demonstrated that during a crack event, the solvent diffused into the epoxy matrix following a non-Fickian case II profile, with a geometrical swelling of the surface layer of the crack. For a healing time of 24h, a critical crack gap of 30μm was identified, beyond which the swelling was insufficient to bridge the crack faces and the healing efficiency was limited to around 25%. For smaller crack gaps, solvent swelling led to intimate contact of the crack faces and reaction of residual functional groups through a reduction of the glass transition temperature Tg of the epoxy, resulting in improved healing efficiency. The use of shape memory alloys (SMA) that are strained during the fracture event and subsequently heated to reduce the crack opening was also investigated. High healing efficiencies were observed and it was found that longer SMA wire activation times further improved the healing efficiency up to almost 80% through improved crack closure and an increased degree of polymerization. The behavior of this material during aging was then investigated in partially cracked samples, guaranteeing small crack gaps. It was found that the premature diffusion of the solvent through the microcapsule membrane into the epoxy matrix led to a decrease in healing efficiency from around 75% in fresh samples, to about 15% in samples aged for 75 days. Increasing the thickness of the polymeric shell of the capsules did not significantly improve performance. Moreover, moisture uptake by the epoxy also contributed to the reduced healing efficiency. Because the healing agent is hydrophobic, a higher water content in the epoxy matrix limited solvent diffusion into the epoxy and hence the extent of healing. A potential solution to the problem of premature diffusion of solvent into the epoxy is suggested to be the use of other shell materials or additional coatings on the capsules. The response of the solvent based self-healing system to dynamic fatigue was also studied. While in static testing, matrix swelling governs crack healing, a different mechanism was observed in the case of dynamic loading. In contrast to the unmodified epoxy, which showed rapid crack propagation under all the conditions investigated, in the presence of the solvent, crack arrest was observed for stress intensities of up to 0.48 MPam1/2. This phenomenon was attributed to crack pinning owing to diffusion of the solvent into the matrix surrounding the crack tip. The elongation at break of the solvated epoxy increased threefold, and the Young’s modulus decreased by more than 50%. Using finite element analysis (FEM) to model the stress distribution around the solvent-infused crack tip, it was shown that the local crack tip stress was reduced by 43%, accounting for this novel toughening effect. While solvent healing performed well in an under-cured matrix and interesting phenomena were observed, a fully cured matrix with a two-component self-healing system may be preferable for real applications because it avoids issues pertaining to premature solvent diffusion. The possibility of encapsulating an amine curing agent in a core-shell structure was therefore investigated as an alternative. A microfluidic glass chip was used to encapsulate a hydrophilic amine/water based curing agent in an acrylate resin shell using ex-situ exposure to UV light. Low viscosity epoxy was encapsulated with UF using a modified agitated emulsion encapsulation technique. Successful self-healing was demonstrated for epoxy specimens containing these microcapsules, along with embedded SMA wires, with healing efficiencies of up to 100% and 40% for low and high temperature curing epoxy, respectively. Overall, this work represents a significant step towards affordable epoxy self-healing materials, the feasibility of solvent and epoxy/amine healing having been successfully demonstrated for an epoxy matrix. The epoxy/amine self-healing system is thought to be particularly promising, considering the early stage of development. Furthermore, the integration of SMA wires proved to improve healing efficiencies dramatically, especially with the epoxy/amine microcapsules. With further optimization and scale-up of the microfluidic encapsulation method, a new low cost self-healing system, and hence potentially compatible with a wide range of polymeric materials, including composites, is therefore within reach because it is based on a commonly used epoxy/amine adhesive.

EPFL2013

Synthesis and Functionalization of Silver Nanoparticles for the Preparation of High Permittivity Nanocomposites

Jose Enrico Quijano Quinsaat

Over the last decade, a growing interest in nanochemistry has emerged due to the interesting features of nanomaterials that vary with size, shape and surface structure. In particular, metal nanoparticles have received much attention due to their properties that enable their use in various scientific disciplines. Although metal nanoparticles exhibit a number of properties that differ from bulk, some properties, such as their infinite permittivity, remain unchanged. As a result, metal nanoparticles have also been used to prepare nanocomposites with polymers in order to provide dielectric materials featuring high permittivities which can be used for applications such as energy storage (capacitors) or as materials for the conversion of electrical energy into mechanical motion (actuators). Despite the large number of publications on the preparation of nanocomposites exhibiting high permittivities which have emerged over the years, there is still room for further improvement in the current materials properties. For instance, dielectric losses are still quite high in some materials, and the use of certain types of filler lead to a large deterioration in the mechanical properties of the nanocomposites, especially with increasing filler content. In addition, a large number of the fillers used for the preparation of the nanocomposites feature poor size and shape control as well as poorly defined surface properties thus adding to the complexity of understanding the resulting material properties. This work tries to address some of the current issues concerning the preparation of dielectric materials. Therefore, silver nanoparticles (AgNPs) were used as filler, while polydimethylsiloxane (PDMS) was employed as the polymeric matrix. The advantages of using AgNPs as filler consist of their relative facile preparation, as well as the possibility of controlling their surface properties due to their resistance towards oxidation and corrosion. The possibility of preparing AgNPs in large amounts with control over the average size of the particles was realized by conducting the polyol synthesis of AgNPs in a Segmented Flow Tubular Reactor (SFTR). A SiO2 layer was grown around the AgNPs to prevent the loss of the insulating nature of the composite due to the formation of conductive pathways, and the thickness dependency of the dielectric properties of the core-shell particles was also investigated in this work. Furthermore, the SiO2 shell also provided the possibility of further surface functionalization, which was conducted in order to compatibilize the core-shell particles with the PDMS matrix. PDMS was chosen as the polymeric matrix due to its good electromechanical properties, which include high elasticity, low viscosity as well as low conductivity and low tangent losses (tan ÎŽ). The resulting nanocomposites featured enhanced permittivities compared to PDMS, while further optimization in the reaction conditions as well as in the processing procedure yielded nanocomposites with high flexibility that can undergo strains as high as 800 % at a silver content of 20 vol%. Other properties such as electric conductivity and the tan ÎŽ were kept low which emphasizes the potential of the nanocomposites to being used as flexible dielectric materials.

EPFL2015