Experimental unconditional preparation and detection of a continuous bound entangled state of light

Among the possibly most intriguing aspects of quantum entanglement is that it comes in free and bound instances. The existence of bound entangled states certifies an intrinsic irreversibility of entanglement in nature and suggests a connection with thermodynamics. In this Letter, we present a first unconditional, continuous-variable preparation and detection of a bound entangled state of light. We use convex optimization to identify regimes rendering its bound character well certifiable, and continuously produce a distributed bound entangled state with an extraordinary and unprecedented significance of more than 10 standard deviations away from both separability and distillability. Our results show that the approach chosen allows for the efficient and precise preparation of multimode entangled states of light with various applications in quantum information, quantum state engineering, and high precision metrology.     

Thermal and photochemical stability of poly(vinyl alcohol)/modified lignin blends

A kraft lignin derivative (KLD) obtained by reaction with p-aminobenzoic acid/phthalic anhydride was blended with poly(vinyl alcohol) (PVA) by solution casting from DMSO. PVA and PVA/KLD films were exposed to ultraviolet radiation (24, 48, and 96 h) and analyzed by thermogravimetry (TG), differential scanning calorimetry (DSC), infrared spectroscopy (FTIR), hydrogen nuclear magnetic resonance (¹H NMR) spectroscopy, and scanning electron microscopy (SEM). PVA films show a loss of thermal stability due to irradiation. PVA/KLD reveals greater thermal stability than PVA and an increase in thermal stability after irradiation. These results suggest that the incorporation of KLD into PVA provides a gain in thermal and photochemical stability. FTIR, ¹H NMR, DSC, and TG results obtained for the blends suggest that intermolecular interactions between PVA and KLD chains are present. SEM micrographs revealed blend miscibility for a KLD blend content of up to 15 wt%, as observed at magnification of 1000 times.     

Exo conformers of N‐(pyridin‐2‐yl)‐ and N‐(pyridin‐3‐yl)norbornene‐5,6‐dicarboximide crystals

Two isomeric pyridine‐substituted norbornenedicarboximide derivatives, namely N‐(pyridin‐2‐yl)‐exo‐norbornene‐5,6‐dicarboximide, (I), and N‐(pyridin‐3‐yl)‐exo‐norbornene‐5,6‐dicarboximide, (II), both C₁₄H₁₂N₂O₄, have been crystallized and their structures unequivocally determined by single‐crystal X‐ray diffraction. The molecules consist of norbornene moieties fused to a dicarboximide ring substituted at the N atom by either pyridin‐2‐yl or pyridin‐3‐yl in an anti configuration with respect to the double bond, thus affording exo isomers. In both compounds, the asymmetric unit consists of two independent molecules (Z′ = 2). In compound (I), the pyridine rings of the two independent molecules adopt different conformations, i.e. syn and anti, with respect to the methylene bridge. The intermolecular contacts of (I) are dominated by C—H...O interactions. In contrast, in compound (II), the pyridine rings of both molecules have an anti conformation and the two independent molecules are linked by carbonyl–carbonyl interactions, as well as by C—H...O and C—H...N contacts.     

Communication: are metallic glasses different from other glasses? A closer look at their high frequency dynamics

Using high resolution inelastic x-ray scattering we studied the collective dynamics of the Pd(77)Si(16.5)Cu(6.5) metallic glass, focusing on the energy-momentum region where the boson peak appears. The dispersion relation and the width of the acoustic excitations are determined showing how the longitudinal acoustic modes maintain their dispersive character for frequencies well above the boson peak frequencies. Moreover, we prove that close to these frequencies there is a softening of the apparent sound speed indicating a failure of the Debye continuum approximation at the boson peak frequencies and challenging previous results on other metallic glasses.     

On bipartite graphs of diameter 3 and defect 2

We consider bipartite graphs of degree Δ≥2, diameter D=3, and defect 2 (having 2 vertices less than the bipartite Moore bound). Such graphs are called bipartite (Δ, 3, ?2) ‐graphs. We prove the uniqueness of the known bipartite (3, 3, ?2) ‐graph and bipartite (4, 3, ?2)‐graph. We also prove several necessary conditions for the existence of bipartite (Δ, 3, ?2) ‐graphs. The most general of these conditions is that either Δ or Δ?2 must be a perfect square. Furthermore, in some cases for which the condition holds, in particular, when Δ=6 and Δ=9, we prove the non‐existence of the corresponding bipartite (Δ, 3, ?2)‐graphs, thus establishing that there are no bipartite (Δ, 3, ?2)‐graphs, for 5≤Δ≤10. © 2009 Wiley Periodicals, Inc. J Graph Theory 61: 271–288, 2009     

Characterization of poly(vinyl acetate)/sugar cane bagasse lignin blends and their photochemical degradation

The acetone-soluble lignin fraction (ASLF) of sugar cane bagasse, from a sugar and alcohol factory residue, was obtained after extraction with formic acid and used to prepare blends with poly(vinyl acetate) (PVAc) by casting. PVAc and ASLF/PVAc blends were irradiated with ultraviolet light (Hg lamp). Blend formation and the irradiation effects were examined through thermal analysis (TG and DSC), scanning electron microscopy, and atomic force microscopy. The DSC results show PVAc glass transition temperature (T _g) shifts because of both, irradiation and ASLF incorporation. Non-irradiated pure PVAc presented a smooth surface, while after UV irradiation, light surface spots are observed. ASLF/PVAc 10/90 and 5/95 blends did not exhibit differences before and after UV irradiation, suggesting that lignin protects PVAc from photochemical degradation.