An All-Optical Access-Metro Interface for Hybrid WDM/TDM PON Based on OBS

A new all-optical access-metro network interface based on optical burst switching (OBS) is proposed. A hybrid wavelength-division multiplexing/time-division multiplexing (WDM/TDM) access architecture with reflective optical network units (ONUs), an arrayed-waveguide-grating outside plant, and a tunable laser stack at the optical line terminal (OLT) is presented as a solution for the passive optical network. By means of OBS and a dynamic bandwidth allocation (DBA) protocol, which polls the ONUs, the available access bandwidth is managed. All the network intelligence and costly equipment is located at the OLT, where the DBA module is centrally implemented, providing quality of service (QoS). To scale this access network, an optical cross connect (OXC) is then used to attain a large number of ONUs by the same OLT. The hybrid WDM/TDM structure is also extended toward the metropolitan area network (MAN) by introducing the concept of OBS multiplexer (OBS-M). The network element OBS-M bridges the MAN and access networks by offering all-optical cross connection, wavelength conversion, and data signaling. The proposed innovative OBS-M node yields a full optical data network, interfacing access and metro with a geographically distributed access control. The resulting novel access-metro architectures are nonblocking and, with an improved signaling, provide QoS, scalability, and very low latency. Finally, numerical analysis and simulations demonstrate the traffic performance of the proposed access scheme and all-optical access-metro interface and architectures     

New insights on the asymmetric hydroboration of perfluoroalkenes

Enantioselective access to Markovnikov regioisomeric perfluoroalcohols is achieved in the presence of chiral cationic rhodium complexes and specific hydroborating reagents.     

AFM as an alternative for Young’s modulus determination in ceramic materials in elastic deformation regime

A novel alternative to the conventional nanoindentation technique for hard materials is presented. An atomic force microscopy probe is used as an indenter, applying loads in the nN range and producing elastic deformations of a few nanometres. This new technique allows a reduction of the different inherent nanoindenter problems. This result in an increase in the quality of the overall results, and thus provide better understanding of the contact mechanism between the indenter and the sample, yielding Young’s modulus values consistent with the literature. This is confirmed by a series of experiments performed on different YBa₂Cu₃O_7?x textured and single crystal samples textured using different techniques.     

Hierarchical clustering of asymmetric networks

Advances in Data Analysis and Classification - This paper considers networks where relationships between nodes are represented by directed dissimilarities. The goal is to study methods that, based...     

A nesting ranging algorithm for a Hybrid WDM/TDM PON with colorless Reflective-ONUs under different distances OLT-ONUs

To reduce costs and cumbersome laser provisioning at the Optical Network Unit (ONU) user level in an access Passive Optical Network (PON), the use of a Reflective-ONU (R-ONU) is a good choice for up-data transmission. An optical carrier is sent by the Optical Line Terminal (OLT) at the Central Office, and a device at the ONU modulates the carrier with the upstream data. This allows all ONUs to be equal and colorless, without a light source in a Hybrid WDM/TDM architecture. A Dynamic Bandwidth Allocation is placed at the OLT, managing the lasers and photodetectors shared by all R-ONUs. The OLT laser and photodetector employed in an up-data transmission must be tuned for each ONU and a particular Round Trip Time (RTT), which is twice the propagation time from OLT to ONU. When an R-ONU is served by a laser, the photodetector must also be available after the RTT to demodulate the up-data. We propose a novel nesting ranging algorithm to deal with large different distances OLT–ONUs avoiding collisions and minimizing the delay under Priority Queuing with Quality of Service (QoS).

From White to Red: Electric‐Field Dependent Chromaticity of Light‐Emitting Electrochemical Cells based on Archetypal Porphyrins

The differences in the electroluminescence (EL) of red‐emitting free‐base ( H2TPP ) and Zn‐metalated ( ZnTPP ) archetypal porphyrins are rationalized in light‐emitting electrochemical cells by means of an electric‐field dependent effect, leading to whitish and reddish devices, respectively. Although H2TPP shows superior electrochemical and photophysical features compared to ZnTPP , devices prepared with ZnTPP surprisingly stand out with a deep‐red EL similar to its photoluminescence (PL), while H2TPP devices feature unexpected whitish EL. Standard arguments such as degradation, device architecture, device mechanism, and changes in the nature of the emitting excited states are discarded. Based on electrochemical impedance spectroscopy and first‐principles electronic structure methods, we provide evidence that the EL originates from two H2TPP regioisomers, in which the inner ring H atoms are placed in collinear and vicinal configurations. The combination of their optical features provides an explanation for both the high‐ and low‐energy EL features. Here, the emitting excited state nature is ascribed to the Q bands, since the Soret excited states remain high in energy. This contrasts to what is traditionally postulated in reports focused on H2TPP lighting devices. Hence, this work provides a new explanation for the nature of the high‐energy EL band of H2TPP that might inspire future works focused on white‐emitting molecular‐based devices.     

Palladium-NHC complexes do catalyse the diboration of alkenes: mechanistic insights

Novel catalytic activation of the B-B bond by palladium(II)-NHC complexes in presence of a mild base (NaOAc) and an excess of diboron reagent enables chemoselective 1,2-diboration of alkenes, suggesting the heterolytic cleavage of diboron rather than oxidative addition of a B-B bond to the metal.     

Determination of pharmaceuticals in soils and sediments by pressurized liquid extraction and liquid chromatography tandem mass spectrometry

The present work describes the development of a sensitive analytical method based on pressurized liquid extraction (PLE) and pre-concentration by solid-phase extraction (SPE), followed by liquid chromatography–electrospray tandem mass spectrometry (LC–ESI-MS/MS) for the determination of seventeen pharmaceuticals in soils and sediments. The method is based on sample homogenisation using Na₂–EDTA washed sand and extraction with water at 90 °C. Special emphasis was placed on the optimization of the extraction procedure to develop a green method that reduces, at a maximum, the use of organic solvents in order to eliminate matrix components during the clean-up. The proposed method was linear in a concentration range from 0.3 to 333 ng g⁻¹, with correlation coefficients higher than 0.993. Method detection (MDLs) and quantification (MQLs) limits ranged from 0.1 to 6.8 ng g⁻¹ and from 0.25 to 23 ng g⁻¹, respectively. Absolute recoveries were analyte dependent, varying between 50% and 105% at the MQL level, except for fenofibrate (40%) and diclofenac (34%). The intra-day and inter-day precision was given by RSD values from 0.7% to 7.9% and from 1.6% to 14.5%, respectively. Acetaminophen, carbamazepine, ciprofloxacin, clofibric acid, codeine, diazepam, fenofibrate, metropolol, ofloxacin and propanolol were detected at concentrations from MDL to 35.62 ng g⁻¹ in soils and sediments from marsh areas. Due to the low recoveries, results for fenofibrate and diclofenac can only be considered as semi-quantitative. The method was fully suitable for the other 15 pharmaceuticals.     

A Study on Corrosion Processes of Archaeological Glass from the Valencian Region (Spain) and its Consolidation Treatment

The combined use of scanning electron microscopy/energy dispersive X-ray microanalysis (SEM/EDX) and square wave voltammetry (SQWV), is used for studying the corrosion processes that have taken place in buried glass from different archaeological sites in the Valencian Region (Spain). The procedures permit a parallel investigation of morphology and chemical composition. Determination of the chemical composition of the glasses and their alteration crust and identification of the elements responsible for the colour has been also carried out using energy dispersive X-ray microanalysis. The electrochemical response of samples attached to paraffin-impregnated graphite electrodes reveals the presence of different iron and manganese oxide species in the browning areas of the corroded glass. Image analysis applied to microphotographs obtained by means of SEM led to the determination of morphological parameters concerning the corrosion phenomena occurring on the surface of the fragments such as thickness of the corrosion layer and its laminated structure. Additionally, measurement of the thickness of the film of polymer used as coating in the consolidation treatments has been carried out using cryo-scanning electron microscopy (cryo-SEM) combined with image analysis.     

On the origin of regio- and stereoselectivity in the rhodium-catalyzed vinylarenes hydroboration reaction

We studied the hydroboration of vinylarenes using rhodium complexes bearing atropoisomeric ligands. For the first time, an NMR spectroscopy study of the styrene and catecholborane addition to the precursor of catalyst [Rh(COD)(L-L)]BF(4), where L-L = (R)-BINAP and (R)-QUINAP, showed evidence of the structure of intermediates involved in the catalytic cycle. On the basis of this evidence, and using DFT calculations and QM/MM strategies, we investigated the origin of regio- and stereoselectivity. We determined the structure and stability of the key intermediates for several ligands and substrates and found excellent agreement between the relative stability of the intermediates and the experimentally observed trends. Using model systems, we analyzed the role of the steric and electronic features of the ligands and the substrates in detail.