Comparison of Spaces of Hardy Type for the Ornstein–Uhlenbeck Operator

Denote by γ the Gauss measure on ℝ ⁿ and by ${\mathcal{L}}${\mathcal{L}} the Ornstein–Uhlenbeck operator. In this paper we introduce a Hardy space \mathfrakh¹g{{\mathfrak{h}}^1}{{\rm \gamma}} of Goldberg type and show that for each u in ℝ ∖ {0} and r > 0 the operator (rI+L)^iu(r{\mathcal{I}}+{\mathcal{L}})^{iu} is unbounded from \mathfrakh¹g{{\mathfrak{h}}^1}{{\rm \gamma}} to L ¹γ. This result is in sharp contrast both with the fact that (rI+L)^iu(r{\mathcal{I}}+{\mathcal{L}})^{iu} is bounded from H ¹γ to L ¹γ, where H ¹γ denotes the Hardy type space introduced in Mauceri and Meda (J Funct Anal 252:278–313, 2007), and with the fact that in the Euclidean case (rI-D)^iu(r{\mathcal{I}}-\Delta)^{iu} is bounded from the Goldberg space \mathfrakh¹\mathbbRⁿ{{\mathfrak{h}}^1}{{\mathbb{R}}^n} to L ¹ℝ ⁿ . We consider also the case of Riemannian manifolds M with Riemannian measure μ. We prove that, under certain geometric assumptions on M, an operator T{\mathcal{T}}, bounded on L ² μ, and with a kernel satisfying certain analytic assumptions, is bounded from H ¹ μ to L ¹ μ if and only if it is bounded from \mathfrakh¹m{{\mathfrak{h}}^1}{\mu} to L ¹ μ. Here H ¹ μ denotes the Hardy space introduced in Carbonaro et al. (Ann Sc Norm Super Pisa, 2009), and \mathfrakh¹m{{\mathfrak{h}}^1}{\mu} is defined in Section 4, and is equivalent to a space recently introduced by M. Taylor (J Geom Anal 19(1):137–190, 2009). The case of translation invariant operators on homogeneous trees is also considered.     

A truncated Newton method in an augmented Lagrangian framework for nonlinear programming

In this paper we propose a primal-dual algorithm for the solution of general nonlinear programming problems. The core of the method is a local algorithm which relies on a truncated procedure for the computation of a search direction, and is thus suitable for large scale problems. The truncated direction produces a sequence of points which locally converges to a KKT pair with superlinear convergence rate.     

Spectral Structure and Doublon Dissociation in the Two-Particle Non-Hermitian Hubbard Model

Strongly-correlated systems in non-Hermitian models are an emergent area of research. Herein, a non-Hermitian Hubbard model is considered, where the single-particle hopping amplitudes on the lattice are not reciprocal, and provide exact analytical results of the spectral structure in the two-particle sector of Hilbert space under different boundary conditions. The analysis unveils some interesting spectral and dynamical effects of purely non-Hermitian nature and that deviate from the usual scenario found in the single-particle regime. Specifically, a spectral phase transition of the Mott-Hubbard band on the infinite lattice is predicted as the interaction energy is increased above a critical value, from an open to a closed loop in complex energy plane, and the dynamical dissociation of doublons, i.e., instability of two-particle bound states, in the bulk of the lattice, with a sudden revival of the doublon state when the two particles reach the lattice edge. Particle dissociation observed in the bulk of the lattice is a clear manifestation of non-Hermitian dynamics arising from the different lifetimes of single-particle and two-particle states, whereas the sudden revival of the doublon state at the boundaries is a striking burst edge dynamical effect peculiar to non-Hermitian systems with boundary-dependent energy spectra, here predicted for the first time for correlated particles.     

Classical limit of the quantized hyperbolic toral automorphisms

The canonical quantization of any hyperbolic symplectomorphismA of the 2-torus yields a periodic unitary operator on aN-dimenional Hilbert space,N=1/h. We prove that this quantum system becomes ergodic and mixing at the classical limit (N,N prime) which can be interchanged with the time-average limit. The recovery of the stochastic behaviour out of a periodic one is based on the same mechanism under which the uniform distribution of the classical periodic orbits reproduces the Lebesgue measure: the Wigner functions of the eigenstates, supported on the classical periodic orbits, are indeed proved to become uniformly speread in phase space.     

Improved extraction of vegetable oils under high-intensity ultrasound and/or microwaves

Ultrasound-assisted extraction (UAE) and microwave-assisted extraction (MAE) techniques have been employed as complementary techniques to extract oils from vegetable sources, viz, soybean germ and a cultivated marine microalga rich in docosahexaenoic acid (DHA). Ultrasound (US) devices developed by ourselves, working at several frequencies (19, 25, 40 and 300 kHz), were used for US-based protocols, while a multimode microwave (MW) oven (operating with both open and closed vessels) was used for MAE. Combined treatments were also studied, such as simultaneous double sonication (at 19 and 25 kHz) and simultaneous US/MW irradiation, achieved by inserting a non-metallic horn in a MW oven. Extraction times and yields were compared with those resulting from conventional procedures. With soybean germ the best yield was obtained with a ‘cavitating tube’ prototype (19 kHz, 80 W), featuring a thin titanium cylinder instead of a conventional horn. Double sonication, carried out by inserting an immersion horn (25 kHz) in the same tube, improved the yield only slightly but halved the extraction time. Almost comparable yields were achieved by closed-vessel MAE and simultaneous US/MW irradiation. Compared with conventional methods, extraction times were reduced by up to 10-fold and yields increased by 50–500%. In the case of marine microalgae, UAE worked best, as the disruption by US of the tough algal cell wall considerably improved the extraction yield from 4.8% in soxhlet to 25.9%. Our results indicate that US and MW, either alone or combined, can greatly improve the extraction of bioactive substances, achieving higher efficiency and shorter reaction times at low or moderate costs, with minimal added toxicity.     

A multi-technique nondestructive approach for characterizing the state of conservation of ancient bookbindings

Journal of Thermal Analysis and Calorimetry - The aim of this work is to evaluate the potentiality of a multi-technique nondestructive approach for characterizing the state of conservation of...     

The Impact of pH on Catalytically Critical Protein Conformational Changes: The Case of the Urease,a Nickel Enzyme

Urease uses a cluster of two Ni^II ions to activate a water molecule for urea hydrolysis. The key to this unsurpassed enzyme is a change in the conformation of a flexible structural motif, the mobile flap, which must be able to move from an open to a closed conformation to stabilize the chelating interaction of urea with the Ni^II cluster. This conformational change brings the imidazole side chain functionality of a critical histidine residue, αHis323, in close proximity to the site that holds the transition state structure of the reaction, facilitating its evolution to the products. Herein, we describe the influence of the solution pH in modulating the conformation of the mobile flap. High-resolution crystal structures of urease inhibited in the presence of N-(n-butyl)phosphoric triamide (NBPTO) at pH 6.5 and pH 7.5 are described and compared to the analogous structure obtained at pH 7.0. The kinetics of urease in the absence and presence of NBPTO are investigated by a calorimetric assay in the pH 6.0–8.0 range. The results indicate that pH modulates the protonation state of αHis323, which was revealed to have pK_a=6.6, and consequently the conformation of the mobile flap. Two additional residues (αAsp224 and αArg339) are shown to be key factors for the conformational change. The role of pH in modulating the catalysis of urea hydrolysis is clarified through the molecular and structural details of the interplay between protein conformation and solution acidity in the paradigmatic case of a metalloenzyme.     

Exploring the Phase-Selective,Green, Hydrothermal Synthesis of Upconverting Doped Sodium Yttrium Fluoride: Effects of Temperature,Time, and Precursors

The aim of this work was i) to develop a hydrothermal, low-temperature synthesis protocol affording the upconverting hexagonal phase NaYF₄ with suitable dopants while adhering to the “green chemistry” standards and ii) to explore the effect that different parameters have on the products. In optimizing the synthesis protocol, short reaction times and low temperatures (below 150 °C) were considered. Yb³⁺ and Er³⁺ ions were chosen as dopants for the NaYF₄ material. Within the context of the second goal, parameters including nature of the precursors, treatment temperature, and treatment time were investigated to afford a pure hexagonal crystalline phase, both in the doped and undoped materials. To fully explore the synthesis results, the prepared materials were characterized from a structural (XRD), compositional (XPS, ICP-MS), and morphological (SEM) point of view. The upconverting properties of the compounds were confirmed by photoluminescence measurements.     

Access to Enantiopure Advanced Intermediates en Route to Madangamines

The synthesis of enantiopure ABCE and ABCD tetracyclic advanced intermediates en route to madangamine alkaloids and studies for the construction of the triunsaturated 15-membered D ring of madangamine B and the saturated 13-membered D ring of madangamine E are reported.