Zn2+ doped ormosil–phosphotungstate hybrid films with enhanced photochromic response

Owing to the wide use of photochromic materials in UV sensors and dosimeters, considerable efforts have been made to increase the UV-response and sensitivity of the existing classes of photochromic materials. In this study, we report a simple sol–gel route for the preparation of highly photochromic transparent films based on ormosil–phosphotungstate hybrid materials. The effect of addition of Zn²⁺ ions on the photochromic response of these hybrid films and the possible mechanism involved is discussed. Compared to the undoped samples, the photochromic response of the Zn²⁺-doped hybrid films increases by 59–237 % depending on the concentration of Zn²⁺ ions added to the sol formulation. No structural or electronic change in the phosphotungstate dye was observed by vibrational spectroscopy or UV spectroscopy, though micro X-ray fluorescence (μ-XRF) analysis showed that the addition of Zn²⁺ in the sol–gel preparations leads to an increase in the amount of phosphotungstate (HPW) incorporated in the dip-coated films. Furthermore, TEM and nano-energy-dispersive X-ray showed formation of nano-agglomerates consisting of Zn and HPW in the Zn²⁺-doped samples. Zn K-edge X-ray absorption near edge structure analysis also confirmed the formation of the salt H_x[Zn(OH₂)₆] _2?xPW₁₂O₄₀. It is suggested that these Zn-phosphotungstate nano-agglomerates get trapped into the ormosil network during films preparation leading to increased concentration of the phosphotungstate anions in the films, in accordance with results from μ-XRF analysis. Raman spectroscopy confirmed that the Keggin structure of HPW is preserved in the hybrid films. FTIR spectra of the matrix part of the samples are identical before and after UV-irradiation, which suggests that the photochromic process does not involve oxidation of the organic functionalities. These highly photochromic hybrid films are promising candidates for the design of practical UV-sensing devices and dosimeters.     

Graphical Linking of MO Multicenter Bond Index and VB Structures. II- 5-c Rings and 6-c Heterocyclic Rings

Through the graphical method proposed, it is possible to create a link between an MO multicenter bond index and VB structures. The value of the index depends on the order of the atoms involved, if there are more than three. For 5-c rings, three basic structures are required; the eventually different values are 12. Unlike the 6-c case, it may happen that different pairs of basic structures are used to build the same polygon. For the 6-c rings, including heteroatoms, the original degeneracy of benzene splits, leading eventually to 60 different I_ring values.     

The parameters of the Lewis metric for the Weyl class

We provide physical interpretation for the four parameters of the stationary Lewis metric restricted to the Weyl class. Matching this spacetime to a completely anisotropic, rigidly rotating, fluid cylinder, we obtain from the junction conditions that one of these parameters is proportional to the vorticity of the source. From the Newtonian approximation a second parameter is found to be proportional to the energy per unit of length. The remaining two parameters may be associated to a gravitational analog of the Aharanov-Bohm effect. We prove, using the Cartan scalars, that the Weyl class metric and static Levi-Civita metric are locally equivalent, i.e., indistinguishable in terms of its curvature.     

Solid-Phase “Self-Hydrolysis” of [Zn(NH3)4MoO4@2H2O] Involving Enclathrated Water—An Easy Route to a Layered Basic Ammonium Zinc Molybdate Coordination Polymer

An aerial humidity-induced solid-phase hydrolytic transformation of the [Zn(NH₃)₄]MoO₄@2H₂O (compound 1@2H₂O) with the formation of [(NH₄)_xH_(1−x)Zn(OH)(MoO₄)]_n (x = 0.92–0.94) coordination polymer (formally NH₄Zn(OH)MoO₄, compound 2) is described. Based on the isostructural relationship, the powder XRD indicates that the crystal lattice of compound 1@2H₂O contains a hydrogen-bonded network of tetraamminezinc (2+) and molybdate (2−) ions, and there are cavities (O₄N₄(μ-H₁₂) cube) occupied by the two water molecules, which stabilize the crystal structure. Several observations indicate that the water molecules have no fixed positions in the lattice voids; instead, the cavity provides a neighborhood similar to those in clathrates. The @ symbol in the notation is intended to emphasize that the H₂O in this compound is enclathrated rather than being water of crystallization. Yet, signs of temperature-dependent dynamic interactions with the wall of the cages can be detected, and 1@2H₂O easily releases its water content even on standing and yields compound 2. Surprisingly, hydrolysis products of 1 were observed even in the absence of aerial humidity, which suggests a unique solid-phase quasi-intramolecular hydrolysis. A mechanism involving successive substitution of the ammonia ligands by water molecules and ammonia release is proposed. An ESR study of the Cu-doped compound 2 (2#dotCu) showed that this complex consists of two different Cu²⁺(Zn²⁺) environments in the polymeric structure. Thermal decomposition of compounds 1 and 2 results in ZnMoO₄ with similar specific surface area and morphology. The ZnMoO₄ samples prepared from compounds 1 and 2 and compound 2 in itself are active photocatalysts in the degradation of Congo Red dye. IR, Raman, and UV studies on compounds 1@2H₂O and 2 are discussed in detail.     

Functionalization of PET and PA6.6 woven fabrics

In the present work as received woven fabrics of polyethylene terephthalate (PET) and polyamide 6.6 (PA6.6) were exposed to a continuous dielectric barrier discharge (DBD), in air at atmospheric pressure, at selected discharge power values and conveyor speeds. The chemical modification of the fabric surface was studied by contact angle analysis, attenuated total reflection (ATR)-FTIR spectroscopy and X-ray photoelectron spectroscopy (XPS). The results confirmed that the treatment changed the fabric surface chemistry, increasing its wettability by polar liquids and its oxygen content. Contact angle results showed different behaviour of the two polymer fabrics toward ageing effects; while PET showed a contact angle increase along the subsequent days of treatment, the PA6.6 fabric maintained its hydrophilicity even 15 days after treatment. The surface morphology analysed by scanning electron microscopy (SEM), did not show any significant difference before and after treatment.     

A Priori and a Posteriori Error Analysis of a Wavelet-Based Stabilization for the Mixed Finite Element Method

We use Galerkin least-squares terms and biorthogonal wavelet bases to develop a new stabilized dual-mixed finite element method for second-order elliptic equations in divergence form with Neumann boundary conditions. The approach introduces the trace of the solution on the boundary as a new unknown that acts also as a Lagrange multiplier. We show that the resulting stabilized dual-mixed variational formulation and the associated discrete scheme defined with Raviart–Thomas spaces are well-posed and derive the usual a priori error estimates and the corresponding rate of convergence. Furthermore, a reliable and efficient residual-based a posteriori error estimator and a reliable and quasi-efficient one are provided.     

Toxicological evaluation in silico and in vivo of secondary metabolites of Cissampelos sympodialis in Mus musculus mice following inhalation

The ethanolic extract of the leaves of Cissampelos sympodialis showed great pharmacological potential, with inflammatory and immunomodulatory activities, however, it showed some toxicological effects. Therefore, this study aims to verify the toxicological potential of alkaloids of the genus Cissampelos through in silico methodologies, to develop a method in LC-MS/MS verifying the presence of alkaloids in the infusion and to evaluate the toxicity of the infusion of the leaves of C. sympodialis when inhaled by Swiss mice. Results in silico showed that alkaloid 93 presented high toxicological potential along with the products of its metabolism. LC-MS/MS results showed that the infusion of the leaves of this plant contained the alkaloids warifteine and methylwarifteine. Finally, the in vivo toxicological analysis of the C. sympodialis infusion showed results, both in biochemistry, organ weights and histological analysis, that the infusion of C. sympodialis leaves presents a low toxicity.     

Assessing the validity of DLPNO-CCSD(T) in the calculation of activation and reaction energies of ubiquitous enzymatic reactions

The domain-based local pair natural orbital coupled-cluster with single, double, and perturbative triples excitation (DLPNO-CCSD(T)) method was employed to portray the activation and reaction energies of four ubiquitous enzymatic reactions, and its performance was confronted to CCSD(T)/complete basis set (CBS) to assess its accuracy and robustness in this specific field. The DLPNO-CCSD(T) results were also confronted to those of a set of density functionals (DFs) to understand the benefit of implementing this technique in enzymatic quantum mechanics/molecular mechanics (QM/MM) calculations as a second QM component, which is often treated with DF theory (DFT). On average, the DLPNO-CCSD(T)/aug-cc-pVTZ results were 0.51 kcal·mol⁻¹ apart from the canonic CCSD(T)/CBS, without noticeable biases toward any of the reactions under study. All DFs fell short to the DLPNO-CCSD(T), both in terms of accuracy and robustness, which suggests that this method is advantageous to characterize enzymatic reactions and that its use in QM/MM calculations, either alone or in conjugation with DFT, in a two-region QM layer (DLPNO-CCSD(T):DFT), should enhance the quality and faithfulness of the results.     

A phenomenological description of shape memory alloy transformation induced plasticity

Transformation induced plasticity is defined as the plastic flow arising from solid state phase transformation processes involving volume and/or shape changes without overlapping the yield surface. This phenomenon occurs in shape memory alloys (SMAs) having significant influence over their macroscopic thermomechanical behavior. This contribution presents a macroscopic three-dimensional constitutive model to describe the thermomechanical behavior of SMAs including classical and transformation induced plasticity. Comparisons between numerical and experimental results attest the model capability to capture plastic phenomena. Both uniaxial and multiaxial simulations are carried out.     

Delta Shock Waves in the Shallow Water System

We consider a Riemann problem for the shallow water system \(u_{t} +\big (v+\textstyle \frac{1}{2}u^{2}\big )_{x}=0\), \(v_{t}+\big (u+uv\big )_{x}=0\) and evaluate all singular solutions of the form \(u(x,t)=l(t)+b(t)H\big (x-\gamma (t)\big )+a(t)\delta \big (x-\gamma (t)\big )\), \(v(x,t)=k(t)+c(t)H\big (x-\gamma (t)\big )\), where \(l,b,a,k,c,\gamma :\mathbb {R}\rightarrow \mathbb {R}\) are \(C^{1}\)-functions of time t, H is the Heaviside function, and \(\delta \) stands for the Dirac measure with support at the origin. A product of distributions, not constructed by approximation processes, is used to define a solution concept, that is a consistent extension of the classical solution concept. Results showing the advantage of this framework are briefly presented in the introduction.