A Novel Coherent Multilevel Combined Phase and Polarization Shift Keying Modulation in Twisted Fibers

This article proposes a novel coherent multilevel modulation model that exploits polarization and phase of the field. This model is based on the possibility of coherent systems to use all the four degrees of freedom of the electromagnetic field. The proposed scheme is able, by applying a suitable twisting process to the optical fiber, to physically confine the polarization and the phase of the transmitted field within the phase sphere. In this way, with the same performances of existing systems, the receiver is considerably simplified because there is no longer need of birefringence tracking circuits.     

Synthesis and characterization of graphene‐containing thermoresponsive nanocomposite hydrogels of poly(N‐vinylcaprolactam) prepared by frontal polymerization

Thermoresponsive poly(N‐vinylcaprolactam) nanocomposite hydrogels containing graphene were successfully prepared by frontal polymerization. High concentration of graphene (5.0 mg/mL) was obtained by direct graphite sonication in the self‐same liquid monomer, thus avoiding any chemical manipulation and obtaining “real” graphene as nanofiller instead of one of its more or less oxidized derivative, which is what generally reported in published reports. Furthermore, the corresponding nanocomposites were obtained without using any solvent to be eventually removed. The materials were fully characterized by RAMAN, SEM, and TEM, and their swelling behavior and rheological properties were investigated. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

Aerobic biotransformation of linear alkylbenzene sulphonates under laboratory conditions

Sulphophenyl carboxylates (SPC) derived from the biodegradation of commercial blends of linear alkylbenzene sulphonates (LAS), were recorded during OECD-301E screening tests under aerobic conditions. Both HPLC-FL and GC-MS were employed to determine biotransformation products. Two well defined groups of detectable SPC were generated: transient compounds, i.e. SPC which degrade very quickly, and compounds more persistent than the parent LAS which required an acclimatization period before their mineralization could take place. The biodegradation of a C10-C13 LAS commercial mixture and of two individual homologs (C11-LAS and C12-LAS) led to the identification of the most persistent SPC which were C6-SPC, C7-SPC and C8-SPC. The C6-SPC turned out to be the homolog which biodegrades most slowly, this suggests that odd LAS homologs are more easily biodegradable.     

The solute-solvent system: solvent constraints on the conformational dynamics of acetylcholine

The objective of this study was to determine if and how a solvent influences internal motions in a solute molecule. Acetylcholine was chosen as the object of study given its interesting molecular structure and major biological significance. Molecular dynamics simulations were carried out in the vacuum (10 ns), water (5 ns), methanol (5 ns), and octanol (1.5 ns). Seven clusters of conformers were identified, namely, +g+g, -g-g, +gt, -gt, t+g, t-g, and tt, where the gauche and trans labels refer to the dihedral angles tau(2) and tau(3), respectively. As expected, the relative proportion of these conformational clusters was highly solvent-dependent and corresponded to a progressive loss of conformational freedom with increasing molecular weight of the solvent. More importantly, the conformational clusters were used to calculate instantaneous and median angular velocity (omega and omega(M), respectively) and instantaneous and median angular acceleration (alpha and alpha(M), respectively). Angular velocity and angular acceleration were both found to decrease markedly with increasing molecular weight of the solvent, i.e., vacuum (epsilon = 1) > water > methanol > octanol. The decrease from the vacuum to octanol was approximately 40% for tau(2) and approximately 60% for tau(3). Such solvent-dependent constraints on a solute's internal motions may be biologically and pharmacologically relevant.     

Enhancement of shake-up structure in alkali-metal-ion exchanged forms of α-Zr(HPO4)2 by sputtering

Mg Kα ESCA spectra of several α-Zr(PO₄)₂M₂ compounds (M = Li⁺, Na⁺, K⁺, Cs⁺) have been obtained. Satellite structure is observed at ～7–8 eV from the main P 2s peak (corresponding to ～15–16 eV from the main Zr 3d_{$\text{5}\text{2}$} peak). The intensity of the satellite depends on the counter-ion intercalated. For a given counter-ion it is strongly increased by sputtering, the rate of increase being also dependent on the counter-ion. This observation is interpreted mainly in terms of electron-defect formation similar to that involved in the formation of colour centres by radiation damage, and subsequent charge-transfer shake-up of the trapped electrons to the electron-deficient phosphorus or Zr(IV) centres.     

Thermodynamic basis for viscoelastic and non-isothermal fracture mechanics

Stability criteria for crack propagation have been analysed which are based on the second law of thermodynamics. The isothermal case has been studied both for elastic and viscoelastic materials. The non-isothermal criteria have been considered with particular attention to a fast adiabatic loading process.The thermodynamic constitutive equations which are demanded and their relationships with the elastic energy have been analyzed.     

Quantum ratchets in dissipative chaotic systems

Using the method of quantum trajectories, we study a quantum chaotic dissipative ratchet appearing for particles in a pulsed asymmetric potential in the presence of a dissipative environment. The system is characterized by directed transport emerging from a quantum strange attractor. This model exhibits, in the limit of small effective Planck constant, a transition from quantum to classical behavior, in agreement with the correspondence principle. We also discuss parameter values suitable for the implementation of the quantum ratchet effect with cold atoms in optical lattices.     

Partially dynamic maintenance of minimum weight hyperpaths

We address the problem of dynamically maintaining minimum weight hyperpaths in a directed hypergraph in a decremental setting. For such a problem, we provide a new efficient algorithm that works for a wide class of hyperpath weight measures. This algorithm explicitly updates minimum weight hyperpaths in

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worst case time under a sequence of L hyperarc weight increments and hyperarc deletions, where C is the maximum weight of minimum hyperpaths in and is the size of the representation of the hypergraph. Hyperpath weight measures are only required to belong to the class of strict weakly superior functions.     

Nitrogen,phosphorus and organics removal in two vertical flow experimental wetlands receiving pretreated municipal wastewater

Pollutants removal in two vertical flow experimental wetlands receiving pre-treated municipal wastewater was investigated. Laboratory investigations using microcosms were also carried out in order to identify key processes regulating pollutants removal. Results obtained from experimental wetlands seem to confirm the ability of a single stage installation, where nitrification and denitrification processes are jointly optimised using a gravel medium, always wet but not saturated with water. Results obtained from microcosm investigations show the prominent role of O2 supply, of microbial activity and of bio-available C from vegetal metabolism in the nitrogen removal.     

On existence of undominated pure strategy Nash equilibria in anonymous nonatomic games: a generalization

In this paper, we generalize the exitence result for pure strategy Nash equilibria in anonymous nonatomic games. By working directly on integrals of pure strategies, we also generalize, for the same class of games, the existence result for undominated pure strategy Nash equilibria even though, in general, the set of pure strategy Nash equilibria may fail to be weakly compact. Received August 2001