A comparison between different optimization criteria for tuned mass dampers design

Tuned mass sampers (TMDs) are widely used strategies for vibration control in many engineering applications, so that many TMD optimization criteria have been proposed till now. However, they normally consider only TMD stiffness and damping as design variables and assume that the tuned mass is a pre-selected value. In this work a more complete approach is proposed and then also TMD mass ratio is optimized. A standard single degree of freedom system is investigated to evaluate TMD protection efficiency in case of excitation at the support. More precisely, this model is used to develop two different optimizations criteria which minimize the main system displacement or the inertial acceleration. Different environmental conditions described by various characterizations of the input, here modelled by a stationary filtered stochastic process, are considered. Results show that all solutions obtained considering also the mass of the TMD as design variable are more efficient if compared with those obtained without it. However, in many cases these solutions are inappropriate because the optimal TMD mass is greater than real admissible values in practical technical applications for civil and mechanical engineering. Anyway, one can deduce that there are some interesting indications for applications in some actual contexts. In fact, the results show that there are some ranges of environmental parameters ranges where results attained by the displacement criterion are compatible with real applications requiring some percent of main system mass. Finally, the present research gives promising indications for complete TMD optimization application in emerging technical contexts, as micromechanical devices and nano resonant beams.     

Evidence for ψ' decays into γπ0 and γη

The decays ψ'→γπ(0), γη and γη' are studied using data collected with the BESIII detector at the BEPCII e(+)e(-) collider. The processes ψ'→γπ(0) and ψ'→γη are observed for the first time with signal significances of 4.6σ and 4.3σ, respectively. The branching fractions are determined to be B(ψ'→γπ(0))=(1.58±0.40±0.13)×10(-6), B(ψ'→γη)=(1.38±0.48±0.09)×10(-6), and B(ψ'→γη')=(126±3±8)×10(-6), where the first errors are statistical and the second ones systematic.     

Very weak solutions to elliptic equations with singular convection term

We study Dirichlet problem for a nonlinear equation with a drift term. Despite the presence of the singular convection term, we establish existence and uniqueness of a solution in spaces larger than the natural one.     

Morphology of IPN-like systems consisting of polyethylene and vinyl polymer

The morphology of an interpenetrating network-like (IPN-like) system consisting of polyethylene (PE) and polystyrene (PS) is compared with an IPN system consisting of PE and polymethacrylate copolymers with different lengths of alkyl groups. In the presence of dodecyl methacrylate (DMA) units in the copolymer network of the IPN-like system, increased homogeneity of the interphase was observed.     

Scattering differentiates Alzheimer disease in vitro

The molecular bases of Alzheimer disease and related neurodegenerative disorders are becoming better understood, but the means for definitive diagnosis and monitoring in vivo remain lacking. Near-infrared optical spectroscopy offers a potential solution. We acquired transmission and reflectance spectra of thin brain tissue slabs, from which we calculated wavelength-dependent absorption and reduced scattering coefficients from 470-1000 nm. The reduced scattering coefficients in the near infrared clearly differentiated Alzheimer from control specimens. Diffuse reflectance spectra of gross brain tissue in vitro confirmed this observation. These results suggest a means for diagnosing and monitoring Alzheimer disease in vivo, using near-infrared optical spectroscopy.     

Insights into the mechanism of electrocatalytic hydrogen evolution mediated by Fe2(S2C3H6)(CO)6: the simplest functional model of the Fe-hydrogenase active site

The di-iron complex Fe2(S2C3H6)(CO)6 (a), one of the simplest functional models of the Fe-hydrogenases active site, is able to electrocatalyze proton reduction. In the present study, the H2 evolving path catalyzed by a has been characterized using density functional theory. It is showed that, in the early stages of the catalytic cycle, a neutral mu-H adduct is formed; monoelectron reduction and subsequent protonation can give rise to a diprotonated neutral species (a-muH-SH), which is characterized by a mu-H group, a protonated sulfur atom, and a CO group bridging the two iron centers, in agreement with experimental IR data indicating the formation of a long-lived mu7-CO species. H2 release from a-muH-SH, and its less stable isomer a-H2 is kinetically unfavorable, while the corresponding monoanionic compounds (a-muH-SH- and a-H2-) are more reactive in terms of dihydrogen evolution, in agreement with experimental data. The key species involved in electrocatalysis have structural features different from the hypothetical intermediates recently proposed to be involved in the enzymatic process, an observation that is possibly correlated with the reduced catalytic efficiency of the biomimetic di-iron assembly.     

Effects of thermal history in the ring opening polymerization of CBT and its mixtures with montmorillonite on the crystallization of the resulting poly(butylene terephthalate)

Differential scanning calorimetry was used to study the thermal characteristics and morphological structure of species produced during the ring opening polymerization of cyclic butylene terephthalate (CBT). Thermal programs consisting of a first ramp heating scan and an isothermal step, followed by cooling and a second ramp heating step, were used to study the effects of thermal history, catalyst (butyl chlorotin dihydroxide) at concentrations between 0.1 and 1.3% (w/w), and the presence of a layered silicate nanofiller (montmorillonite at 4.0%, w/w) on the structure of the resulting polymer (poly(butylene terephthalate), pCBT). Wide angle X-ray diffraction was used to monitor the degree of exfoliation of the nanocomposites.It was found that pCBT is formed in the amorphous state, and crystallizes during the heating step or during the isothermal step at temperatures lower than the equilibrium melting temperature of the polymer (). When premixed with the nanofiller, irrespective of whether this was previously intercalated with a tallow surfactant or used in its pristine form, polymerization took place at higher temperatures and most of the crystallization was found to occur during the cooling stage. In those cases where crystallization took place during either the first heating scan, or during a prolonged isothermal step below the of the polymer, the resulting crystals were found to have a higher lamellar thickness, as compared with the same polymer crystallized from the melt during the cooling step from temperatures above the polymer .     

Rough set approach to multiple criteria classification with imprecise evaluations and assignments

Dominance-based Rough Set Approach (DRSA) has been introduced to deal with multiple criteria classification (also called multiple criteria sorting, or ordinal classification with monotonicity constraints), where assignments of objects may be inconsistent with respect to dominance principle. In this paper, we consider an extension of DRSA to the context of imprecise evaluations of objects on condition criteria and imprecise assignments of objects to decision classes. The imprecisions are given in the form of intervals of possible values. In order to solve the problem, we reformulate the dominance principle and introduce second-order rough approximations. The presented methodology preserves well-known properties of rough approximations, such as rough inclusion, complementarity, identity of boundaries and precisiation. Moreover, the meaning of the precisiation property is extended to the considered case. The paper presents also a way to reduce decision tables and to induce decision rules from rough approximations.     

Proton reduction and dihydrogen oxidation on models of the [2Fe]H cluster of [Fe] hydrogenases. A density functional theory investigation

Density functional theory was used to compare reaction pathways for H2 formation and H+ reduction catalyzed by models of the binuclear cluster found in the active site of [Fe] hydrogenases. Terminal H+ binding to an Fe(I)-Fe(I) form, followed by monoelectron reduction and protonation of the di(thiomethyl)amine ligand, can conveniently lead to H2 formation and release, suggesting that this mechanism could be operative within the enzyme active site. However, a pathway that implies the initial formation of Fe(II)-Fe(II) mu-H species and release of H2 from an Fe(II)-Fe(I) form is characterized by only slightly less favored energy profiles. In both cases, H2 formation becomes less favored when taking into account the competition between CN and amine groups for H+ binding, an observation that can be relevant for the design of novel synthetic catalysts. H2 cleavage can take place on Fe(II)-Fe(II) redox species, in agreement with previous proposals [Fan, H.-J.; Hall, M. B. J. Am. Chem. Soc. 2001, 123, 3828] and, in complexes characterized by terminal CO groups, does not need the involvement of an external base. The step in H2 oxidation characterized by larger energy barriers corresponds to the second H+ extraction from the cluster, both considering Fe(II)-Fe(II) and Fe(II)-Fe(III) species. A comparison of the different reaction pathways reveals that H2 formation could involve only Fe(I)-Fe(I), Fe(II)-Fe(I), and Fe(II)-Fe(II) species, whereas Fe(III)-Fe(II) species might be relevant in H2 cleavage.     

Charmed hadrons from coalescence plus fragmentation in relativistic nucleus-nucleus collisions at RHIC and LHC

In a coalescence plus fragmentation approach we calculate the heavy baryon/meson ratio and the \(p_T\) spectra of charmed hadrons \(D^{0}\), \(D_{s}\) and \(\varLambda _{c}^{+}\) in a wide range of transverse momentum from low \(p_T\) up to about 10 GeV and discuss their ratios from RHIC to LHC energies without any change of the coalescence parameters. We have included the contribution from decays of heavy hadron resonances and also the one due to fragmentation of heavy quarks which do not undergo the coalescence process. The coalescence process is tuned to have all charm quarks hadronizing in the \(p_T\rightarrow 0\) limit and at finite \(p_T\) charm quarks not undergoing coalescence are hadronized by independent fragmentation. The \(p_T\) dependence of the baryon/meson ratios are found to be sensitive to the masses of coalescing quarks, in particular the \(\varLambda _{c}/D^{0}\) can reach values of about \(\mathrm 1\div 1.5 \) at \(p_T \approx \, 3\) GeV, or larger, similarly to the light baryon/meson ratio like \(p/\pi \) and \(\varLambda /K\), however a marked difference is a quite weak \(p_T\) dependence with respect to the light case, such that a larger value at intermediate \(p_T\) implies a relatively large value also for the integrated yields. A comparison with other coalescence model and with the prediction of thermal model is discussed.