Multiple agents finitely repeated inspection game with dismissals

Decision makers usually have to face a budget and other type of constraints when they have to decide which projects are going to be undertaken (to satisfy their requirements and guarantee profitable growth). Our purpose is to assist them in the task of selecting project portfolios. We have approached this problem by proposing a general nonlinear binary multi-objective mathematical model, which takes into account all the most important factors mentioned in the literature related with Project Portfolio Selection and Scheduling. Due to the existence of uncertainty in different aspects involved in the aforementioned decision task, we have also incorporated into the model some fuzzy parameters, which allow us to represent information not fully known by the decision maker/s. The resulting problem is both fuzzy and multiobjective. The results are complemented with graphical tools, which show the usefulness of the proposed model to assist the decision maker/s.     

Competitive C-I versus C-CN reductive elimination from a Rh(III) complex. Selectivity is controlled by the solvent

The RhIII complex [(PNP)Rh(CN)(CH3)][I] 5, obtained by oxidative addition of methyl iodide to [(PNP)Rh(CN)] 2, reacts selectively in two pathways: In aprotic solvents C-I reductive elimination of methyl iodide followed by its electrophilic attack on the cyano ligand takes place, giving the methyl isonitrile RhI complex [(PNP)Rh(CNCH3)][I] 3, while in protic solvents C-C reductive elimination of acetonitrile takes place forming an iodo RhI complex [(PNP)RhI] 9. Reaction of 2 with ethyl iodide in aprotic solvents gave the corresponding isonitrile complex, while in protic solvents no reactivity was observed. The selectivity of this reaction is likely due to a hydrogen bond between the cyano ligand and the protic solvent, as observed by X-ray diffraction, which retards electrophilic attack on this ligand.     

Assembly of crystalline halogen-bonded materials by physical vapor deposition

Polycrystalline halogen-bonded assemblies fabricated by physical vapor deposition (PVD) exhibit controllable morphologies and microstructures. Although the solid-state packing may vary going from a solution crystal growth process (used for chromophore single-crystal determination) to a vapor-phase deposition process (used for PVD film fabrication), the corresponding film microstructures are independent of the substrate surface chemistry.     

Pricing decisions in a dual supply chain of organic and conventional agricultural products

Annals of Operations Research - We analyze a dual-channel supply chain comprising two suppliers that offer vertically-differentiated agricultural products; specifically, one offers an organic...     

Minimal average degree aberration and the state polytope for experimental designs

For a particular experimental design, there is interest in finding which polynomial models can be identified in the usual regression set up. The algebraic methods based on Gröbner bases provide a systematic way of doing this. The algebraic method does not, in general, produce all estimable models but it can be shown that it yields models which have minimal average degree in a well-defined sense and in both a weighted and unweighted version. This provides an alternative measure to that based on “aberration” and moreover is applicable to any experimental design. A simple algorithm is given and bounds are derived for the criteria, which may be used to give asymptotic Nyquist-like estimability rates as model and sample sizes increase.     

Enzymes in a golden cage

We describe a general method for the entrapment of enzymes within bulk metallic gold. This is a new approach for the immobilization of enzymes on metals, which is commonly carried out by 2D adsorption or covalent biding, that is, the enzyme is in contact with the metal at a specific contact zone of the enzyme, while most of the rest of it remains exposed to the environment. The 3D metallic encaging of the enzymes is quite different: the enzyme is in contact with the metallic cage walls all around it and is well protected inside. The porous nature of the metallic matrix enables substrate molecules to diffuse inside, reach the active site, and let product molecules diffuse out. The generality of the approach was proven by the successful entrapment of five enzymes representing different classes and different bio- and medical applications: l-asparaginase (Asp), collagenase, horseradish peroxidase (HRP), laccase and glucose oxidase (GOx). GOx–gold conjugates have been of particular interest in the literature. The main challenge we had to solve was how to keep the enzyme active in the process of gold-synthesis from its cation – this required careful tailoring of reaction conditions, which are detailed in the paper. The gold entrapped enzymes gain thermal stability and protectability against harsh conditions. For instance, we could keep Asp alive at the extreme pH of 13, which normally kills the enzyme instantly. The entrapped enzymes obey the Michaelis–Menten kinetics, and activation energies were determined. Good recyclability for eight cycles was found. Multi-enzymatic reactions by combinations of the off-the-shelf bioactive enzyme@gold powders are possible, as demonstrated for the classical detection of GOx activity with HRP. Detailed material characterization and proposed mechanisms for the 3D protectability of the enzymes are provided. The new enzyme immobilization method is of wide potential uses in medicine, biotechnology, bio-fuel cells and enzymatic (electro)sensing applications.

We describe a general method for the entrapment of enzymes within bulk metallic gold.     

Phase transitions in O/W lauryl acrylate emulsions during phase inversion,studied by light microscopy and cryo-TEM

Phase changes during the preparation of nano-emulsions containing polymerizable monomer as the oil phase, by the phase inversion temperature technique (PIT), were investigated using light microscopy, cryo-TEM and viscosity measurements. The nano-emulsions were prepared using a poly(oxyethylene) nonionic surfactant and a polymerizable acrylic monomer (lauryl acrylate) as the oil phase. Inversion of the emulsion, followed by rapid cooling, resulted in emulsions having an average droplet size as low as 25 nm. Cryo-TEM was used to observe the structures that are present above and below the phase transition temperature, and gave, for the first time, visual indication of the presence of a microemulsion and a locally ordered structure in the process. At high surfactant concentrations, the inversion–cooling process yields emulsions with unique structures, in which the oil phase is present as worm-like structures.     

Porphine and pyrrole-substituted porphyrin from cyclocondensation of tripyrrane with mono-substituted pyrroles

The condensation of non-substituted tripyrrane with mono-substituted pyrroles did not lead to corrole, but to porphine and 5-pyrrolyl-porphyrin. Both compounds were fully characterized by a combination of spectroscopic methods and X-ray crystallography.     

Assessing the mechanical,phase inversion,and rheological properties of poly-[(R)-3-hydroxybutyrate-co-(R)-3-hydroxyvalerate] (PHBV) blended with poly-(l-lactic acid) (PLA)

Poly-(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) and poly-(l-lactic acid) (PLA) have attracted much interest in recent years since they are biodegradable, thus can replace synthetic non-degradable materials. In this study, improvements of PHBV, mechanical, phase inversions, and rheological properties were investigated after blending with PLA in varying ratio’s. Three different blends of commercially available PLAs with 92–98% l-lactide units and one grade of PHB with 5% valerate content were blended using a micro-compounder at 175 °C. The composition of PHBV in blends ranged from 50% to 80%. With the addition of PLA, increases in the flexural strength and elastic modulus were observed for several blends, while minor to no changes were detected in the elongation at break and tensile strength as compared to pure PHBV material. Like many conventional plastics, the complex viscosity decreased with increasing rotational frequency due to decreasing entanglements and molecular weight. The complex viscosity with respect to time was very stable for the blends, but no improvements in the PHBV viscosity were observed with the addition of PLA at 170 °C. Three phase inversion models were used to predict the continuity of the blends, and the results showed both dual- and PLA-continuity phase for the blends. In summary, the mechanical results showed improvements in the tensile and flexural properties, while the rheological observation showed minor improvements in the complex viscosity for numerous concentrations.