Analytical, numerical and experimental study of the finite inflation of circular membranes

In the present work we derive an analytical expression for the pressure–deflection curve of circular membranes subjected to inflation. This problem has been studied mostly from a numerical point of view and there is still a lack of accurate closed-form solutions in nonlinear elasticity. The analytical formulation is developed with a semi-inverse method by setting a priori the kinematics of deformation of the membrane. A compressible Mooney–Rivlin material model is considered and a pressure–deflection relation is derived from the equilibrium. The kinematics is approximated and therefore the obtained solution is not exact. Consequently, the formulation is adjusted by introducing an additional polynomial function in the pressure–deflection equation. The polynomial is calibrated by fitting numerical solutions of the exact system of differential equilibrium equations. The calibration is done over a wide range of constitutive parameters that covers the response of all rubber materials for technological applications. As a result, a definitive and accurate expression of the applied pressure as a function of the deflection of the membrane is obtained. The formula is validated with finite element (FE) simulations and compared with other solutions available in the literature. The comparison shows that the present model is more accurate. In addition, unlike the other models, it can be applied to compressible materials. Experimental uniaxial and bulge tests are carried out on rubber materials and the model proposed is used to characterize the Mooney–Rivlin constitutive parameters. Since the pressure–deflection formula is accurate and easy-to-use, it is an innovative tool in engineering applications of inflated membranes

Interface bonding of a ferromagnetic/semiconductor junction : a photoemission study of Fe/ZnSe(001)

We have probed the interface of a ferromagnetic/semiconductor (FM/SC) heterojunction by a combined high resolution photoemission spectroscopy and x-ray photoelectron diffraction study. Fe/ZnSe(001) is considered as an example of a very low reactivity interface system and it expected to constitute large Tunnel Magnetoresistance devices. We focus on the interface atomic environment, on the microscopic processes of the interface formation and on the iron valence-band. We show that the Fe contact with ZnSe induces a chemical conversion of the ZnSe outermost atomic layers. The main driving force that induces this rearrangement is the requirement for a stable Fe-Se bonding at the interface and a Se monolayer that floats at the Fe growth front. The released Zn atoms are incorporated in substitution in the Fe lattice position. This formation process is independent of the ZnSe surface termination (Zn or Se). The Fe valence-band evolution indicates that the d-states at the Fermi level show up even at submonolayer Fe coverage but that the Fe bulk character is only recovered above 10 monolayers. Indeed, the Fe 1-band states, theoretically predicted to dominate the tunneling conductance of Fe/ZnSe/Fe junctions, are strongly modified at the FM/SC interface.Comment: 23 pages, 5 figures, submitted to Physical review

A degrading bouc-wen data-driven model for the cyclic behavior of masonry infilled RC frames

Mechanics-based macro-models are often used to simulate the cyclic response of infilled reinforced concrete (RC) frames. However, these approaches are affected by uncertainties regarding damage and failure mechanisms. Therefore, this contribution proposes a new smooth data-driven model for the hysteresis of infilled RC frames. The infill panel is modeled through a damage-based Bouc-Wen element, which accounts for both pinching and deterioration of the mechanical characteristics. The parameters of the model are calibrated from an experimental data set of cyclic responses of RC infilled frames. Analytical correlations between parameters and geometric and mechanical characteristics of the infilled frame are derived. Blind validation tests are carried out in order to demonstrate the effectiveness of the proposed model

Defect Engineering of Ta3N5 Photoanodes: Enhancing Charge Transport and Photoconversion Efficiencies via Ti Doping

While Ta3N5 shows excellent potential as a semiconductor photoanode for solar water splitting, its performance is hindered by poor charge carrier transport and trapping due to native defects that introduce electronic states deep within its bandgap. Here, it is demonstrated that controlled Ti doping of Ta3N5 can dramatically reduce the concentration of deep-level defects and enhance its photoelectrochemical performance, yielding a sevenfold increase in photocurrent density and a 300 mV cathodic shift in photocurrent onset potential compared to undoped material. Comprehensive characterization reveals that Ti4+ ions substitute Ta5+ lattice sites, thereby introducing compensating acceptor states, reducing the concentrations of deleterious nitrogen vacancies and reducing Ta3+ states, and thereby suppressing trapping and recombination. Owing to the similar ionic radii of Ti4+ and Ta5+, substitutional doping does not introduce lattice strain or significantly affect the underlying electronic structure of the host semiconductor. Furthermore, Ti can be incorporated without increasing the oxygen donor content, thereby enabling the electrical conductivity to be tuned by over seven orders of magnitude. Thus, Ti doping of Ta3N5 provides a powerful basis for precisely engineering its optoelectronic characteristics and to substantially improve its functional characteristics as an advanced photoelectrode for solar fuels applications

Dynamics of surface magnetization on a nanosecond time scale

The dynamics of surface magnetization is measured with ns time resolution by spin-polarimetry of the total photoemission yield excited by synchrotron radiation pulses. The surface response is compared to the bulk magnetization dynamics as obtained by induction measurements. The surface and the bulk show distinct magnetization dynamics indicating weak coupling during the reversal process in the (Formula presented) time domain. Ultrathin layers of Fe as well as three-layer Fe/Cu/Fe exchange coupled structures were grown on top of an amorphous soft-ferromagnetic substrate (Vitrovac) and showed different reversal dynamics

Personalized medicine in rheumatology : the paradigm of serum autoantibodies

The sequencing of the human genome is now well recognized as the starting point of personalized medicine. Nonetheless, everyone is unique and can develop different phenotypes of the same disease, despite identical genotypes, as well illustrated by discordant monozygotic twins. To recognize these differences, one of the easiest and most familiar examples of biomarkers capable of identifying and predicting the outcome of patients is represented by serum autoantibodies. In this review, we will describe the concept of personalized medicine and discuss the predictive, prognostic and preventive role of antinuclear antibodies (ANA), anti-citrullinated peptide antibodies (ACPA), rare autoantibodies and anti-drug antibodies (ADA), to evaluate how these can help to identify different disease immune phenotypes and to choose the best option for treating and monitoring rheumatic patients in everyday practice. The importance of ANA resides in the prediction of clinical manifestations in systemic sclerosis and systemic lupus erythematosus and their association with malignancies. ACPA have a predictive role in rheumatoid arthritis, they are associated with the development of a more aggressive disease, extra-articular manifestations and premature mortality in RA patients; moreover, they are capable of predicting therapeutic response. Rare autoantibodies are associated with different disease manifestations and also with a greater incidence of cancer. The determination of ADA levels may be useful in patients where the clinical efficacy of TNF-\u3b1 inhibitor has dropped, for the assessment of a right management. The resulting scenario supports serum autoantibodies as the cornerstone of personalized medicine in autoimmune diseases

Accuracy of synovial fluid analysis compared to histology for the identification of calcium pyrophosphate crystals: An ancillary study of the OMERACT US working group - CPPD subgroup

The aim of this study was to evaluate the accuracy of synovial fluid analysis in the identification of calcium pyrophosphate dihydrate crystals compared to microscopic analysis of joint tissues as the reference standard. This is an ancillary study of an international, multicentre cross-sectional study performed by the calcium pyrophosphate deposition disease (CPPD) subgroup of the OMERACT Ultrasound working group. Consecutive patients with knee osteoarthritis (OA) waiting for total knee replacement surgery were enrolled in the study from 2 participating centres in Mexico and Romania. During the surgical procedures, synovial fluid, menisci and hyaline cartilage were collected and analysed within 48 hours from surgery under transmitted light microscopy and compensated polarised light microscopy for the presence/absence of calcium pyrophosphate crystals. All slides were analysed by expert examiners on site, blinded to other findings. A dichotomic score (absence/presence) was used for scoring both synovial fluid and tissues. Microscopic analysis of knee tissues was considered the gold standard. Sensitivity, specificity, accuracy, positive and negative predictive values of synovial fluid analysis in the identification of calcium pyrophosphate crystals were calculated.15 patients (53% female, mean age 68 yo +/- 8.4) with OA of grade 3 or 4 according to Kellgren-Lawrence scoring were enrolled. 12 patients (80%) were positive for calcium pyrophosphate crystals at the synovial fluid analysis and 14 (93%) at the tissue microscopic analysis. The overall diagnostic accuracy of synovial fluid analysis compared with histology for CPPD was 87%, with a sensitivity of 86% and a specificity of 100%, the positive predictive value was 100% and the negative predictive value was 33%.In conclusion synovial fluid analysis proved to be an accurate test for the identification of calcium pyrophosphate dihydrate crystals in patients with advanced OA