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The use of rheology and terminal flow relaxation times to predict healing behavior at long healing times is by now quite well accepted. In this work we go one step further and explore the use of macro-rheology (in particular the stored work of deformation) to predict the early stage interfacial healing properties (fracture resistance) of a set of self-healing polyurethanes. https://www.selleckchem.com/products/levofloxacin-hydrochloride.html The interfacial healing is measured by single edge notch fracture experiments, using short healing times and a low healing temperature to exclude the effect of long range molecular motion on mechanical properties restoration. The systems based on aromatic diisocyanates show high fracture resistance after healing, while very limited restoration of the mechanical properties is observed for aliphatic and cycloaliphatic based polyurethanes. Linear sweep rheology and time-temperature-superposition allow obtaining the macro-rheological master curve and the mechanical relaxation spectra (H(t)). The application of a recently established deconvolution protocol to the H(t) gives the characteristic relaxation times and stored works of deformation associated to individual dynamic processes such as segmental motion, reversible bonds, and terminal flow. It is found that the calculated stored works of deformation related to the reversible bond relaxation reproduce the trend observed by fracture resistance at healed interfaces and reveal a qualitative correspondence between reversible bonds work of deformation and interfacial healing fracture resistance. Moreover, the method seems to point to the existence of a threshold interfacial work of deformation below which no efficient load transfer can be observed.Artificial enzymes have drawn substantial research interest from the scientific community due to their advantages over natural enzymes. However, majority of artificial enzymes exhibit low affinity towards H2O2, which means that a high H2O2 concentration is needed for the oxidation of a substrate such as 3,3',5,5'-tetramethylbenzidine (TMB) to blue-colored oxTMB. With this concern, Cu-CuFe2O4 was facilely synthesized, wherein, Cu0 accelerates the redox capacity of Cu-CuFe2O4 as well as the electron transfer between CuFe2O4 and H2O2. These materials induce excellent activity as a peroxidase. Cu-CuFe2O4 shows high affinity towards H2O2 with lower Michaelis-Menten constant (Km) than the reported values for ferrites and Horseradish enzyme (HRP). Moreover, it took only 5 min to detect hydrogen peroxide (H2O2) and glutathione (GSH) through a colorimetric assay using Cu-CuFe2O4. Compared with CuFe2O4, the limit of detection (LOD) is about 90-fold lower for H2O2 using Cu-CuFe2O4. In addition, Cu-CuFe2O4 shows high stability as a nanozyme. Thus, the mechanism of the peroxidase-like nanozyme Cu-CuFe2O4 is proposed.Understanding transport mechanisms of electrons and phonons, two major energy carriers in solids, are crucial for various engineering applications. It is widely believed that more free electrons in a material should correspond to a higher thermal conductivity; however, free electrons also scatter phonons to lower the lattice thermal conductivity. The net contribution of free electrons has been rarely studied because the effects of electron-phonon (e-ph) interactions on lattice thermal conductivity have not been well investigated. Here an experimental study of e-ph scattering in quasi-one-dimensional NbSe3 nanowires is reported, taking advantage of the spontaneous free carrier concentration change during charge density wave (CDW) phase transition. Contrary to the common wisdom that more free electrons would lead to a higher thermal conductivity, results show that during the depinning process of the condensed electrons, while the released electrons enhance the electronic thermal conductivity, the overall thermal conductivity decreases due to the escalated e-ph scattering. This study discloses how competing effects of free electrons result in unexpected trends and provides solid experimental data to dissect the contribution of e-ph scattering on lattice thermal conductivity. Lastly, an active thermal switch design is demonstrated based on tuning electron concentration through electric field.A chronological account is given to the development of a full range interatomic potential. Starting with a simple phenomenological model, the terms in the model are gradually modified, so that they can carry some definite physical meaning. To gain insight, a systematic, order by order interaction potential theory is developed. Conversely, this theory suggests the functional form for the potential model. At present, we have a simple interaction model that is capable of describing the van der Waals potentials of many systems from R = 0 to R → ∞.Developing convenient and sensitive detection methods for antibiotic residues in food is beneficial for ensuring food quality and human health. The tough challenges that limit the development of sensitive, quantitative, portable, on-the-spot antibiotic detectors are the lack of simple and effective target recognition and signal amplification strategies, and direct digital quantification. Herein, we developed a visual digital quantitative aptasensor, based on a binding-induced 3-D DNA nanomachine signal probe, for the simple and sensitive, on-the-spot detection of antibiotics.In the present study, the utility of Pr3+/Pr4+ and Bi3+/Bi(0) redox couples for oxidation and reduction reactions is demonstrated by synthesizing bismuth-substituted PrO1.833 samples following a solution combustion method. The samples retained the defect fluorite structure of PrO1.833 with the inclusion of up to 40 mol% of bismuth, beyond which the rhombohedral structure emerged. The microscopic analysis also reinforced the defect fluorite structure of these samples. The lattice expanded with the inclusion of bismuth. The samples had porous morphology, and the X-ray energy dispersive spectral analysis ensured the presence of Pr and Bi closer to the nominal molar ratio. The intense band at 565 cm-1 in the Raman spectrum shifted to higher values with a progressive increase in bismuth content due to the creation of more oxygen vacancies. In Pr0.60Bi0.40O2-δ, Pr existed in +3 and +4 oxidation states, as revealed by the X-ray photoelectron spectral analysis. The photoluminescence spectra consisted of 4f-4f transitions of Pr3+ and emission in the blue region (due to oxygen vacancies).
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