On an equilibrium problem with complementarity constraints formulation of pay-as-clear electricity market with demand elasticity

We consider a model of pay-as-clear electricity market based on a Equilibrium Problem with Complementarity Constraints approach where the producers are playing a noncooperative game parameterized by the decisions of regulator of the market (ISO). In the proposed approach the bids are assumed to be convex quadratic functions of the production quantity. The demand is endogenously determined. The ISO problem aims to maximize the total welfare of the market. The demand being elastic, this total welfare take into account at the same time the willingness to pay of the aggregated consumer, as well as the cost of transactions. The market clearing will determine the market price in a pay-as-clear way. An explicit formula for the optimal solution of the ISO problem is obtained and the optimal price is proved to be unique. We also state some conditions for the existence of equilibria for this electricity market with elastic demand. Some numerical experiments on a simplified market model are also provided.     

A General Nonconvex Multiduality Principle

We introduce a (possibly infinite) collection of mutually dual nonconvex optimization problems, which share a common optimal value, and give a characterization of their global optimal solutions. As immediate consequences of our general multiduality principle, we obtain Toland–Singer duality theorem as well as an analogous result involving generalized perspective functions. Based on our duality theory, we propose an extension of an existing algorithm for the minimization of d.c. functions, which exploits Toland–Singer duality, to a more general class of nonconvex optimization problems.     

Ureasil–polyether hybrid blend with tuneable hydrophilic/hydrophobic features based on U-PEO1900 and U-PPO400 mixtures

Urea-cross-linked polyether-siloxane hybrid blends with tuneable hydrophilic/hydrophobic features were prepared from a mixture of poly(ethylene oxide) (PEO1900) and poly(propylene oxide) (PPO400), hybridized by end-chain functionalization with (3-isocyanatopropyl)triethoxysilane. The aim of this study was to demonstrate that the combination of the different polyether phases produces materials with hydrophilic and hydrophobic properties. An anti-fog coating and a transparent monolithic swellable hydrogel were produced from the PEO1900 hybrid. Swellability and drug release profiles could be easily tuned by varying the ureasil–PEO/ureasil–PPO ratio in the hybrid matrix. Differential scanning calorimetry (DSC) and small angle X-ray scattering (SAXS) analyses indicated that the nanostructure of the hybrid blends could be described by the existence of a biphasic mixture of PEO1900-rich and PPO400-rich phases, with a fraction of the lamellar domains being derived from the PEO1900 crystallinity. A correlation between the nanoscopic features and the kinetics of the swelling mechanism is proposed, based on the results of in situ SAXS analyses. In vitro monitoring using UV–Vis spectroscopy indicated that the kinetics of drug release from the PEO1900:PPO400 hybrid blends could be controlled by varying the proportions of the hydrophilic (PEO1900) and hydrophobic (PPO400) hybrids. The response to pH change and to application of a magnetic field to the PEO1900-magnetite nanocomposite indicated that the production of stimuli-responsive delivery devices based on ureasil–PE should be feasible in the near future.     

The Glucosamine-derivative NAPA Suppresses MAPK Activation and Restores Collagen Deposition in Human Diploid Fibroblasts Challenged with Environmental Levels of UVB

The ultraviolet (UV) component of solar radiation is the driving force of life on earth, but it can cause photoaging and skin cancer. In this study, we investigated the effects of the glucosamine-derivative 2-(N-Acetyl)-L-phenylalanylamido-2-deoxy-β-D-glucose (NAPA) on human primary fibroblasts (FBs) stimulated in vitro with environmental levels of UVB radiation. FBs were irradiated with 0.04 J cm⁻² UVB dose, which resulted a mild dosage as shown by the cell viability and ROS production measurement. This environmental UVB dose induced activation of MAP kinase ERK 1/2, the stimulation of c-fos and at lower extent of c-jun, and in turn AP-1-dependent up-regulation of pro-inflammatory factors IL-6 and IL-8 and suppression of collagen type I expression. On the contrary, 0.04 J cm⁻² UVB dose was not able to stimulate metalloprotease production. NAPA treatment was able to suppress the up-regulation of IL-6 and IL-8 via the inhibition of MAP kinase ERK phosphorylation and the following AP-1 activation, and was able to attenuate the collagen type I down-regulation induced by the UVBs. Taken together, our results show that NAPA, considering its dual action on suppression of inflammation and stimulation of collagen type I production, represents an interesting candidate as a new photoprotective and photorepairing agents.     

Chiral ferrocenyl ligands with bidentate pyridine donors. Synthesis and application in Pd-catalyzed asymmetric allylic alkylation of 1,3-diphenylpropenyl-1-esters

A synthetic procedure relying on the Friedländer condensation of enantiopure α-amino ferrocenecarboxaldeyde has been devised for the regio-designed elaboration of a pyridine nucleus fused onto the ferrocene scaffold. Three novel bidentate ligands with different pyridine nitrogen donors featuring the [3,2-b]ferrocenopyridine fragment a as the sole chirogenic element have been prepared in enantiopure form through a multi step route involving the diastereoselective deprotonation of a chiral acetal of ferrocenecarboxaldehyde in the stereodetermining step. The ligands were assessed in the Pd-catalyzed allylic alkylation of 1,3-diphenyl-2-propenyl esters with good stereoselectivity.     

New Copoly(bisphenol-A)carbonates,Having Hydrophilic Porphyrin Units as End-Groups,Synthesized by Melt-Reacting Processes

The synthesis of some poly(bisphenol-A)carbonates (PCs) containing hydrophilic porphyrin units as end groups, by thermal treatment of commercial PC and 5,10,15-tri{p[ω-methoxy-poly(oxyethylene)]phenyl}20(p-hydroxy phenyl)porphyrin (I) blends, is reported. A suitable choice of reaction temperature, molar composition and reaction time, allowing the extent of the outer-inner transesterification reactions, leads to a gradual insertion of porphyrin units in the polymer chains. The composition of the obtained materials was inferred by GPC and MALDI-TOF mass spectrometric analysis.     

Functionalization of Biodegradable Polyester for Tissue Engineering Applications

Summary: Chemical modification of polymer surface may potentially be used to create smart materials that can guide cellular adhesion, proliferation and maintenance of specific expression of molecules. The microbial polyester poly (3-hydroxybutyrate) (PHB) has been attracted attention as promising material for applications in tissue engineering. In this work, a wet-chemical method, base ethylenediamine aminolysis, was performed to improve the adhesion of chondrocytes isolated from human articular cartilage to PHB films. The effects of chemical treatment on PHB films was evaluated by following changes in morphology and surface chemical composition using atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS), respectively. While the effect on cells morphology was studied by scanning electron microscopy (SEM). The treatment with ethylenediamine did not change significantly the morphology of the structures of PHB films surface. However, the roughness of the aminolyzed films was slightly higher. The introduction of nitrogen-containing groups was confirmed by XPS. In vitro experiments indicated that the surface modification did not have toxic effects in cells, since they could adhere and proliferate on modified PHB films. It was observed that long-time treatment improved ability of PHB films to support cell growth, which could be accounted to physicochemical and topological effects.     

Sui morfismi di spazi analitici formali

Riassunto In questa nota si dimostra che un morfismo adico fra spazi analitici formali è finito se e solo se è quasi-finito; si dimostra inoltre un teorema di coerenza delle immagini dirette per morfismi 1-convessi fra spazi analitici formali.

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Summary In this paper we prove that an adic morphism between formal analytic spaces is finite if and only if it is quasi-finite; moreover we establish a direct image theorem for 1-convex morphisms between formal analytic spaces.

     

A Multicomponent Model of Chromophoric Dissolved Organic Matter Photobleaching¶§

Light absorption by chromophoric dissolved organic matter (CDOM) plays a number of roles in natural waters, including both control of the underwater light field and the initiation of many photochemical reactions. A multicomponent analysis was used to describe the effects of UV and visible radiation on the optical absorption spectra of two natural water samples, a Suwannee River fulvic acid standard (SRFA) and a Delaware Bay water sample. This analysis used a constrained minimization technique to fit independent spectral components to the observed bleaching behavior of the water samples under monochromatic irradiation. Spectra derived from these fits were used to predict the bleaching behavior of both samples under polychromatic irradiation (λ< 320 nm). This approach reproduces the kinetics and spectral behavior of polychromatic photobleaching very well at times <48 h, but underpredicts the bleaching at longer time periods.