Here the synthesis of hydroxy-telechelic four-arm star-shaped oligotetrahydrofuran (4PTHF) with controllable molecular weight was explored, which was perfomed as living cationic ring-opening polymerization of THF using pentaerythritol and trifluoromethanesulfonicanhydride as initiation system. The molecular weights of the 4PTHF were a function of the reaction time. A polymer network was prepared from the hydroxy-telechelic 4PTHF precursor by crosslinking with diisocyanate and the shape-memory properties were determined. High values for R f and R r > 98% were obtained even at high programmed elongations, which suggest the 4PTHF-network as a promising shape-memory material. These materials might have a great potential, as the upscaling of synthesis could be successfully demonstrated.

Multimillion-atom reactive molecular dynamics simulations were used to investigate the mechanisms which control heat-initiated oxidation in aluminum nanoparticles. The simulation results reveal three stages: (1) confined burning, (2) onset of deformation, and (3) onset of small cluster ejections. The first stage of the reaction is localized primarily at the core-shell boundary, where oxidation reactions result in strong local heating and the increased migration of oxygen from the shell into the core. When the local temperature rises above the melting point of alumina (T=2330K), the melting of the shell allows deformation of the overall particle and an increase in heat production. Finally, once the particle temperature exceeds 2800-3000 K, small aluminum-rich clusters are ejected from the outside of the shell. The underlying mechanisms were explored using global and radial statistical analysis, as well as developed visualization techniques and localized fragment analysis.

The three-stage reaction mechanism found here provides insight into the controlling factors of aluminum nanoparticle oxidation, a topic of considerable importance in the energetic materials community.

Investigation of lanthanum cerium oxide as a gate oxide on 4H-SiC was performed by varying post-deposition annealing temperature from 400 to 1000°C. Energy band alignment and band gap of bulk oxide and interfacial layer (IL) with respect to SiC were extracted using X-ray photoelectron microscopy. Two band alignment structures were proposed and the change of band alignment was affected by the changes in chemical composition in bulk oxide and in IL that may induce lattice strains and dipoles. A conduction band offset of IL/SiC was 0.97 eV for sample annealed at 1000°C, which was comparable to the value extracted from Fowler-Nordheim model. The acquisition of sufficient conduction band offset, coupled with the lowest slow trap density, effective oxide charges, interface trap density, as well as total interface trap density, yielded the lowest leakage current density for this sample.

The aim of the present research work is to investigate the influence of B addition on the phase transformation kinetics under continuous cooling conditions. In order to perform this study, the behavior of two low carbon advanced ultra-high strength steels (A-UHSS) is analyzed during dilatometry tests over the cooling rate range of 0.1-200°C/s. The start and finish points of the austenite transformation are identified from the dilatation curves and then the continuous cooling transformation (CCT) diagrams are constructed. These diagrams are verified by microstructural characterization and Vickers micro-hardness. In general, results revealed that for slower cooling rates (0.1-0.5 °C/s) the present phases are mainly ferritic-pearlitic (F+P) structures. By contrast, a mixture of bainitic-martensitic structures predominates at higher cooling rates (50-200°C/s). On the other hand, CCT diagrams show that B addition delays the decomposition kinetics of austenite to ferrite, thereby promoting the formation of bainitic-martensitic structures. In the case of B microalloyed steel, the CCT curve is displaced to the right, increasing the hardenability. These results are associated with the ability of B atoms to segregate towards austenitic grain boundaries, which reduce the preferential sites for nucleation and development of F+P structures.

Theoretical calculations were performed on 2, 5-aromatic substituted pyrroles which have a nitro-benzene or a cyano-benzene link to the nitrogen atom of the pyrrol fragment. The molecules manifested interesting semiconductor behavior that was confirmed when thin films were prepared and their corresponding electrical characterization undertaken. The reason for this behavior is discussed, with reference to the electron withdrawing feature of the substituents in the benzene chain.

The effect of stress on the deformation and crack nucleation and propagation mechanisms of a γ-TiAl intermetallic alloy (Ti-45Al-2Nb-2Mn (at.%) - 0.8v.%TiB2) was studied by means of in situ tensile (constant strain rate) and tensile-creep (constant load) experiments performed at 973 K inside a scanning electron microscope (SEM). The evolution of the microstructure and the nucleation and propagation of cracks was tracked during the high temperature mechanical tests in the SEM. Colony boundary crack nucleation was found to be activated during the secondary stage in creep tests at 300 MPa and 400 MPa and during the tertiary stage of the creep tests performed at higher stresses and at constant strain rate. Interlamellar ledges were only observed during the high stress tensile-creep tests (σ>400 MPa) and during the constant strain rate test. Quantitative measurements of the nature of the crack propagation path along secondary cracks and along the primary crack were carried out. It was found that colony boundaries were preferential sites for crack propagation under all the conditions investigated. The frequency of interlamellar cracking increased with increasing stress.

In order to establish defined biomimetic systems, type I collagen was functionalised with 1,3-Phenylenediacetic acid (Ph) as aromatic, bifunctional segment. Following investigation on molecular organization and macroscopic properties, material functionalities, i.e. degradability and bioactivity, were addressed, aiming at elucidating the potential of this collagen system as mineralization template. Functionalised collagen hydrogels demonstrated a preserved triple helix conformation. Decreased swelling ratio and increased thermo-mechanical properties were observed in comparison to state-of-the-art carbodiimide (EDC)-crosslinked collagen controls. Ph-crosslinked samples displayed no optical damage and only a slight mass decrease (∼ 4 wt.-%) following 1-week incubation in simulated body fluid (SBF), while nearly 50 wt.-% degradation was observed in EDC-crosslinked collagen. SEM/EDS revealed amorphous mineral deposition, whereby increased calcium phosphate ratio was suggested in hydrogels with increased Ph content. This investigation provides valuable insights for the synthesis of triple helical collagen materials with enhanced macroscopic properties and controlled degradation. In light of these features, this system will be applied for the design of tissue-like scaffolds for mineralized tissue formation.

We report our main results on the development of un-cooled microbolometers based on hydrogenated amorphous Germanium-Silicon (a-GexSiy:H) thermo-sensing films deposited by Plasma Enhanced Chemical Vapor Deposition (PECVD). Our research has been conducted to improve both, the structure of the devices (pixels) and the performance characteristics of the amorphous Germanium-Silicon thermosensing films.

Our motivation is to produce microbolometers with much better performance characteristics (larger thermal coefficient of resistance, larger conductivity and better stability) than those available in commercial microbolometer arrays, based on boron doped hydrogenated amorphous silicon (a-Si:H,B).

As part of our latest research, we also report the study of what we believe is the next generation of thermosensing films based on Silicon and Geranium amorphous films with embedded nanocrystals in the amorphous matrix (polymorphous films). Those materials have several advantages over amorphous, as a lower defect density, better stability and better transport properties.

Nanoparticles (NPs) loaded with human platelet-derived growth factor (h-PDGF) were prepared and characterized. These NPs were co-assembled with collagen to form highly aligned NP-collagen composite fibers by using an electrochemical process. PDGF can be released gradually from either NPs or aligned NP-collagen fibers. This investigation demonstrated a novel way to fabricate highly aligned composite fibers, which can locally release a growth factor in a controlled and gradual manner, potentially avoiding the fast clearance of the growth factor from the implantation site. Thus, the aligned NP-collagen fiber is a novel and promising implantation material for tendon/ligament repair and regeneration.

Plutonium and Pu-Ga alloys have been observed to have anomalous hydrogen solubility behavior, including a significant concentration dependence of hydrogen diffusivity in the dilute regime, a sharp drop off in the hydrogen solubility constant in the dilute regime, and a near complete absence of change in the Sieverts’ constant as the alloys are heated across phase transformation boundaries. We are investigating the possibility that a vacancy mechanism is responsible for this behavior. X-ray diffraction measurements show a 0.14% lattice contraction in Pu-2 at. % Ga alloys when they are charged with ~2 at. % hydrogen. The lattice re-expands when the hydrogen is removed. Density functional calculations show that increasing the number of hydrogen atoms associated with a vacant lattice site in Pu lowers the energy of the hydrogen-vacancy complex. These observations support the idea that vacancies are stabilized by hydrogen in the Pu lattice well beyond their thermal equilibrium concentration and could be responsible for the anomalous hydrogen response of Pu.

Stacked layered pin a-SiC/a-Si devices based on a filter design are approached from a reconfigurable point of view. This paper shows that a double SiC/Si pin photodiode can be de-composed into two photonic active filters changeable in function. Reconfiguration is provided by optical control signals to the optoelectronic front and back pin building blocks. Depending on the wavelength and irradiation side of the external optical bias the device acts either as a short- and a long- pass band filter or as a band-stop filter, amplifying or rejecting a specific wavelength range. Particular attention is given to the amplification coefficient weights, which allow taking into account the wavelength background effects. We illustrate these effects in detail and discuss the filters transfer function characteristics. We present examples of filters and we propose a reconfigurable device for directed optical logic. An algorithm to decode the information is presented. An optoelectronic model supports the optoelectronic logic architecture.

Important pore structure parameters related to mechanical properties and durability of cement-based materials can be determined by techniques such as scanning electron microscopy (SEM), mercury intrusion porosimetry (MIP), and low temperature calorimetry (LTC). The methods provide information on porosity characteristics as pore volume, pore thresholds and/or pore size distribution in different size ranges and do therefore to a large extent supplement each other. Pastes of w/b=0.4 with 0%, 40% or 70% slag by volume were cured saturated at 20ºC for up to two years. The porosity was characterized by LTC, MIP, and SEM. Higher volume of pores was obtained by MIP compared to results obtained using LTC and SEM. Measured porosity was correlated with predicted porosity using information on the density and degree of hydration of the cement and slag. Porosity estimation showed best agreement with the porosity data measured by MIP. The use of slag showed the same trend for all tests: a higher total volume of pores, but a lower threshold pore size when compared with Portland cement paste. The findings illustrate the importance of measuring not only pore volume but also threshold pore sizes when characterizing porosity of cement-based materials with different binder compositions.

Self-curing, or internal curing (IC), technology has been developed to counteract self-desiccation and autogenous shrinkage of high-strength/high-performance concrete (HSC/HPC), which is considered the "Achilles’ hill" of HSC/HPC [1]. According to ACI [2], IC refers to the process by which the hydration of cement continues because of the availability of internal water that is not part of the mixing water; while the internal water is made available by the pore system in structural lightweight aggregate (LWA) that absorbs and releases water. Recently ACI defined internal curing as “supplying water throughout a freshly placed cementitious mixture using reservoirs, via pre-wetted lightweight aggregates, that readily release water as needed for hydration or to replace moisture lost through evaporation or self-desiccation” [3]. Both definitions address the use of pre-wetted LWA as a self-curing (or internal curing) agent.

According to the definition of the RILEM Technical Committee TC-196 [4], IC implies introduction to the concrete mixture a component, which serves as a curing agent. This agent can be either a normal aggregate introduced into the concrete mixture in water-saturated state or a new component (for example, an additive or special aggregate). Similarly to the division accepted in external curing, RILEM TC-196 distinguishes between two categories of internal curing: (a) internal water curing (sometimes called “water entrainment”), when the curing agent performs as a water reservoir, which gradually releases water, and (b) internal sealing, when the curing agent is intended to delay/prevent loss of water from the hardening concrete. Although water-saturated porous aggregate is still the most popular material among IC agents, super-absorbent polymers (SAP), ceramic waste, recycled aggregate and wood-derived products show promising properties. In view of this, self-curing covers not only use of pre-wetted LWA, but also other methods of curing: water curing by means of variety of curing agents introduced in the concrete mix, and also the methods based on internal sealing.

The recent achievements in methods and materials for self-curing are reviewed, and the future trends in development of self-curing concrete are discussed.

The analysis of the structures and microstructures of nanostructured thin layers can be performed using laboratory grazing incidence diffraction, provided accurate corrections are performed to handle the instrumental broadening effects related to the experiment geometry for an impinging beam close to the critical angle. Implementing these corrections in Rietveld refinement software allows the accurate extraction of quantitative relevant information about the structure (strain and atomic positions) and the microstructure (crystallite size and microstrain), selectively probing the material on a depth of few nanometers.

In this paper was study the effect of heat treatment on mechanical properties of an API X-60 steel used for storage and transportation of hydrocarbons. In the first stage evaluation are mechanical properties of steel heat treated by the technique of the three-point test according to ASTM 399-90 was carried out. In the second stage, characterization of the type of failure and microstructure through optical microscopy (OM) was determined; also heat treated samples were then mechanically tested for hardness (HRC) and nano-indentation. The presence of alloying elements by scanning electron microscopy (SEM) and the fracture surfaces generated in the steel with varying times, temperatures and cooling medium generated by different modes of solicitation (Bending), likewise with loading rates were determined. The results revealed a ductile fracture and microstructures (PF) ferrite-pearlite (DP), bainite -ferrite (BF) and martensite-retained and martensite/retained austenite (MA). Finally, this article discusses the effect of heat treatment followed by precipitation hardenable of steel API X-60 on the mechanical properties

The electronic transport properties of the organic ferroelectric gate field-effect transistors (FeFETs) with the ZnO channel were investigated. The FeFETs with the channel thickness below 100 nm show nonvolatile operation and the on/off ratio of 105. The field-effect mobility decreased with decreasing the channel thickness. From the Hall-effect measurement, it was found that the Hall mobility increases and the carrier concentration decreases after the deposition of the organic ferroelectric gate. From these results, the effect of the ferroelectric polarization on the electronic transport in the FeFETs was discussed.

Position-dependent force-detected NMR measurements on a 25x15x7 μm3 single crystal of ammonium sulfate (NH4)2SO4 were performed at room temperature in a sample-on-oscillator configuration. Force signals were detected with 12 μm resolution in a one-dimensional scan. Measurements of NMR relaxation times T2* = 1.5 ± 0.3 μs, T2 = 44 ± 2 μs, and T1 = 5.6 ± 0.7 s were obtained in an 8-T magnetic field, revealing an unexpected frequency-dependent fluctuation spectrum at room temperature.

We show that graphene mono-/bilayer step operates as an abrupt p-n (p-p+) junction. Due to the thickness-dependent oxidation effect, the uniform channel can be adjusted to spatially asymmetrical junction by means of electron beam irradiation. The lithography-free process on OTMS modified substrate possesses the merit of clean surface and high performance. This conveniently fabricated graphene step device opens an opportunity to study the intrinsic interface across a well defined junction.

It has been reported [1] that microwave radiation can enhance many of the mechanical properties of Bombyx mori silkworm cocoon silk, as measured in constant strain rate tensile tests to failure and in stress relaxation tests. The consequences of microwave radiation will affect decisions about the use of silk in settings subjected to significant microwave exposure – for example, as a reinforcing fiber in an epoxy matrix composite that may be microwave cured, or as a component in aircraft radomes.

There are two possible mechanisms by which microwave radiation may affect a material [2]: (i) the radiation may enable chemical and/or microstructural changes – and therefore property changes – in the same way that conventional heating would, or (ii) the high heating rates that are achievable by microwaving may selectively favor changes that would be masked under conventional conditions, where heating rates are low enough to give preference to changes that have a lower activation energy. Here we explore the former possibility for silk.

We characterized several mechanical properties of degummed and subsequently annealed B. mori silk, and compared them to the corresponding properties of degummed B. mori silk that was not annealed. The annealing treatment was carried out at 140 °C for 7 hours (conditions that optimally increased crystal size in an unrelated study of B. mori silk [3]), and then the fibers were allowed to cool gradually to room temperature over the course of an hour. Comparison of mechanical properties revealed no differences between the materials that we tested. Thus, for annealed silk, we do not observe the enhancements that can be achieved by microwaving. We conclude that in cases where microwaving affects the properties of silk, those changes are not a simple consequence of annealing by the microwaves.