Ethernet-based passive optical local-area networks for fiber-to-the-desk application

We introduce optical local-area network (LAN) architectures based on multimode optical fiber and components, short wavelength lasers and detectors, and the widely used fast Ethernet protocol. These architectures are designed to lower the costs associated with passive optical LAN implementation. Further reduction in overall cost is achieved through decreased network downtime, lower maintenance cost, extended geometrical spans, and larger headroom for future capacity increase. These optically transparent networks represent a novel approach for implementing fiber-to-the-desk.     

Electrospun curcumin/polycaprolactone/copolymer F-108 fibers as a new therapy for wound healing

The application of fibers associated with drugs is a promising alternative to meet the clinical needs of tissue repair. Curcumin exhibits great cicatricial potential because it has numerous pharmacological properties. This research aimed to produce fibers of polycaprolactone and copolymer F-108 associated with curcumin and to evaluate in vivo their action on the process of wound healing. The fibers were produced by electrospinning technique and characterized by scanning electron microscopy (SEM), X-ray diffractometry (XRD), and fluorescence microscopy. They were applied in cutaneous wounds of rats for the analysis of photoacoustic permeation and histological study. The characterization showed that the electrospinning allowed the preparation of homogeneous material with curcumin. The fibers benefited healing of the wounds and allowed the permeation of curcumin at all stages. The use of PCL/F-108 fibers allowed the elaboration of a new curcumin delivery system, improving its bioavailability and action in the healing of excisional wound. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48415.     

Enhancement of the photoelectrochemical response of poly(terthiophenes) by CdS(ZnS) core-shell nanoparticles

We have investigated the photoelectrochemical properties of hybrid films of polythiophenes poly(4,4″dimethoxy-3′-methyl-2,2′:5′,2″ terthiophene) (PDM), poly(4,4″dipentoxy-3′-methyl-2,2′:5′,2″ terthiophene) (PDP), and cadmium sulfide/zinc sulfide (CdS(ZnS)) core-shell nanoparticles. Although CdS(ZnS) nanoparticles present enhanced exciton trapping, light harvesting by hybrid films was enhanced when compared to those of pure PDM and PDP films. This enhancement is explained in terms of electron and hole transfer mechanisms at different excitation wavelengths. The more efficient light harvesting of PDM/CdS(ZnS) when compared to that of PDP/CdS(ZnS) was attributed to its broader absorption spectrum and more efficient electron hopping.     

Surface modification of polystyrene and poly(ethylene terephtalate) by grafting poly(N-isopropylacrylamide)

In this work, poly(N-isopropylacrylamide) (PNIPAAm) was incorporated into previously oxidized PS and PET surfaces by grafting using two photo-initiation pathways. The incorporation of PNIPAAm was observed by drop water contact angle measurements, dyeing with Methylene Blue and AFM images analysis of the virgin and modified polymers. It was verified that the grafting process depends on the chemical surface environment. The grafted surfaces are hydrophilic below 32 °C and hydrophobic above this temperature. The transition is due to the incorporated PNIPAAm. This characteristic gives to the grafted materials potential to be applied as biomaterials.     

Development of composites based on recycled polyethylene/sugarcane bagasse fibers

In this work, sugarcane bagasse fibers were used as filler in composites having recycled high‐density polyethylene (PEr) as matrix. Because of the poor interaction between fibers surface and the PEr, the surface of bagasse was chemically modified. This modification consists of washing with water at 80°C, a mercerization process using sodium hydroxide and acetylation reaction with acetic anhydride. The chemical modification was characterized by Fourier transform infrared–horizontal attenuated total reflectance (FTIR‐HATR) and ¹³C nuclear magnetic resonance spectroscopies (NMR), thermogravimetric analysis (TGA), and scanning electronic microscopy (SEM). The composites were prepared from modified and unmodified fibers into PEr matrix, containing 5, 10, and 20% (w/w) of fiber. The samples were processed by extrusion and molds were prepared by injection process in order to perform mechanical tests. These materials were analyzed by SEM, TGA, and the water uptake was evaluated. Also, their mechanical properties were analyzed. Morphological analysis indicated that the chemical modification of sugarcane bagasse increased the compatibility between matrix and reinforcement. Tensile, flexural, and impact tests showed that the mechanical properties of the composite were improved compared to PEr due to the presence of the fibers. POLYM. COMPOS., 35:768–774, 2014. © 2013 Society of Plastics Engineers     

Optimal design of GaN-AlGaN Bragg-confined structures for intersubband absorption in the near-infrared spectral range

A method is proposed for the design and optimization of structural parameters of GaN-AlGaN Bragg-confined structures with respect to peak intersubband absorption from the ground to the first excited state,1 /spl rarr/ 2 electronic transition, in the near infrared spectral range. An above-the-barrier bound state was used to extend the range of transition energies above the values available in conventional quantum wells. Intrinsic polarization fields and nonparabolicity effects were taken into account. The selection of optimal parameters, maximizing the absorption at wavelengths of 1.55 and 1.3 /spl mu/m, was performed by using a simulated annealing algorithm, and optimal structures with infinite superlattices as confinement regions were thus designed. These optimal parameters were then used to set realistic, finite structures with a small number of layers, the performance of which was re-evaluated by solving the Schrodinger-Poisson equation self-consistently for a few different levels and profiles of doping.     

Investigation of the morphological changes promoted by heating of Si–C–O ceramics derived from a phenyl-rich hybrid polymer. Effect of Ni in the polymeric precursor

This study focuses on the structural and morphological changes promoted by heating of silicon oxycarbide ceramics obtained from hybrid polymeric precursors based on poly(methylsiloxane) and divinylbenzene, with or without nickel acetate, by pyrolysis under Ar at different temperatures. The increase of the temperature from 950 to 1500 °C promoted the densification and crystallization of SiC and graphite nanodomains in the ceramic bulk with or without Ni, as identified by HRTEM. Moreover, the Ni-containing precursor led to the formation of ultra-long amorphous nanowires on the surface and voids in the ceramic body obtained at 1500 °C. These nanowires presented different sizes and morphologies, but similar compositions, basically composed by silicon and oxygen, with the presence of carbon at their external layers. The growth mechanism and the nature of the nanowires are also proposed. The addition of nickel acetate in the polymeric precursor induced the formation of nanowires with different morphologies in the Si–O–C system.     

Defensive responding on the MMPI-2 in family custody and access evaluations.

The objective of this study was to examine defensive underreporting on the Minnesota Multiphasic Personality Inventory-2 (MMPI-2) with a sample of parents involved in custody dispute litigation. With a composite score derived from 2 nontraditional validity indicators—the Wiggins Social Desirability scale (WSD) and the Superlative scale (S), which had previously been identified as the best predictors of fake-good responding, 74% of litigants were identified as underreporting compared with 52% identified using traditional Lie (L) and Correction (K) scale criterion. Litigants identified as underreporters whether using either the WSD-S criterion or the L-K criterion, had clinical scale profiles that were similar to those identified as nonunderreporters. The outcome of this study suggests that the WSD and S scales are perhaps more useful in the identification of defensive underreporting than the L and K scales. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Hippocampal and Reticulo-Thalamic Parvalbumin Interneurons and Synaptic Re-Organization during Sleep Disorders in the Rat Models of Parkinson’s Disease Neuropathology

We investigated the alterations of hippocampal and reticulo-thalamic (RT) GABAergic parvalbumin (PV) interneurons and their synaptic re-organizations underlying the prodromal local sleep disorders in the distinct rat models of Parkinson’s disease (PD). We demonstrated for the first time that REM sleep is a predisposing state for the high-voltage sleep spindles (HVS) induction in all experimental models of PD, particularly during hippocampal REM sleep in the hemiparkinsonian models. There were the opposite underlying alterations of the hippocampal and RT GABAergic PV+ interneurons along with the distinct MAP2 and PSD-95 expressions. Whereas the PD cholinopathy enhanced the number of PV+ interneurons and suppressed the MAP2/PSD-95 expression, the hemiparkinsonism with PD cholinopathy reduced the number of PV+ interneurons and enhanced the MAP2/PSD-95 expression in the hippocampus. Whereas the PD cholinopathy did not alter PV+ interneurons but partially enhanced MAP2 and suppressed PSD-95 expression remotely in the RT, the hemiparkinsonism with PD cholinopathy reduced the PV+ interneurons, enhanced MAP2, and did not change PSD-95 expression remotely in the RT. Our study demonstrates for the first time an important regulatory role of the hippocampal and RT GABAergic PV+ interneurons and the synaptic protein dynamic alterations in the distinct rat models of PD neuropathology.     

Release of BSA from porous matrices constituted of alginate–Ca and PNIPAAm-interpenetrated networks

The synthesis of thermosensitive Interpenetrating Polymer Network (IPN) hydrogels and the release of Bovine Serum Albumin (BSA) from the hydrogels were reported. The hydrogels, constituted of poly(N-isopropyl acrylamide) PNIPAAm network interpenetrated in alginate–Ca²⁺ network, were synthesized in a two-stepped process. In the first step, PNIPAAm network was synthesized from an aqueous solution containing N-isopropyl acrylamide (NIPAAm) monomers and N,N′-methylene-bis-acrylamide (MBAAm) co-monomers, and sodium alginate (SA) (1 or 2% w/v). The concentration of NIPAAm monomers in the hydrogel-forming solution was always 2.5, 5.0 or 10.0% (w/v). In the second step, alginate–Ca²⁺ networks were formed by immersion of the membrane, obtained on the first step, in a 1.0% (w/v) aqueous calcium chloride. The IPN hydrogels were characterized as a function of temperature (from 25 to 45 °C) through the following measurements: drop water contact angle (DWCA), compression elastic modulus (E) and cross-linking density (ν_e). The morphology was investigated using scanning electronic microscopy (SEM). In vitro release of BSA from the hydrogels was monitored by UV–Vis spectroscopy at 22 °C and 37 °C. DWCA results showed a decrease in the hydrogel hydrophilicity when the temperature and/or the PNIPAAm amount on hydrogels were increased. PNIPAAm-loader hydrogels are more compacted and presented elevated rigidity, mainly above 35 °C. This trend was attributed to the collapsing of PNIPAAm chains as the hydrogels were warmed above its Lower Critical Solution Temperature (LCST), which in aqueous solution is ca. 32–33 °C. The amount of BSA released from the alginate–Ca²⁺/PNIPAAm hydrogels changes inversely to both amount of PNIPAAm and temperature. The transport of BSA from the hydrogels was evaluated through a conventional model. In the lesser-compacted hydrogels the release occurs mostly by diffusion. In the more compacted ones the chain relaxation contributes to the BSA release. Thus, the alginate–Ca²⁺/PNIPAAm IPN-typed matrixes may be considered as smart hydrogels for the release of BSA, because the amount and rate of BSA released may be tailored by both the NIPAAm concentration in the hydrogel-forming solution and the control of temperature of hydrogel.