Conducting graft copolymers of pyrrole and thiophene with random copolymers of methyl methacrylate and 3-methylthienyl methacrylate

Random copolymers of 3-methyl thienylmethacrylate and methyl methacrylate were synthesized via free radical polymerization. Electro-copolymerizations of random copolymers with thiophene and/or pyrrole were carried out in acetonitrile-tetrabutylammonium tetrafluoroborate (TBAFB), water-p-toluene sulfonic acid (PTSA) solvent-electrolyte couples. Oxidative polymerization of thiophene functionalized random copolymer was also achieved by constant current electrolysis and chemical polymerization. The characterizations were done by conductivity measurements, cyclic voltammetry (CV), Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermal gravimetry analysis (TGA), scanning electron microscopy (SEM).     

A multi-stage stochastic programming approach in master production scheduling

Master Production Schedules (MPS) are widely used in industry, especially within Enterprise Resource Planning (ERP) software. The classical approach for generating MPS assumes infinite capacity, fixed processing times, and a single scenario for demand forecasts. In this paper, we question these assumptions and consider a problem with finite capacity, controllable processing times, and several demand scenarios instead of just one. We use a multi-stage stochastic programming approach in order to come up with the maximum expected profit given the demand scenarios. Controllable processing times enlarge the solution space so that the limited capacity of production resources are utilized more effectively. We propose an effective formulation that enables an extensive computational study. Our computational results clearly indicate that instead of relying on relatively simple heuristic methods, multi-stage stochastic programming can be used effectively to solve MPS problems, and that controllability increases the performance of multi-stage solutions.     

Speciation of Iron in Soils and the Relation with Its Concentration in Fruits

An attempt was made to identify the iron species that is most responsible for plant-available Fe. Iron concentrations in fruit samples were determined by using flame atomic absorption spectrometry (FAAS). The soil samples related to these fruits were also analyzed for Fe by using various digestion and extraction reagents. The relation between the fruit-Fe and soil-extractable-Fe concentrations was examined to explain the Fe uptake of fruit from soil. The probable chemical forms of Fe in the soil were evaluated for the speciation of Fe.     

Global and local expression of chirality in serine on the Cu{110} surface

Establishing a molecular-level understanding of enantioselectivity and chiral resolution at the organic-inorganic interfaces is a key challenge in the field of heterogeneous catalysis. As a model system, we investigate the adsorption geometry of serine on Cu{110} using a combination of low-energy electron diffraction (LEED), scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. The chirality of enantiopure chemisorbed layers, where serine is in its deprotonated (anionic) state, is expressed at three levels: (i) the molecules form dimers whose orientation with respect to the substrate depends on the molecular chirality, (ii) dimers of L- and D-enantiomers aggregate into superstructures with chiral (-1 ?2; 4 0) lattices, respectively, which are mirror images of each other, and (iii) small islands have elongated shapes with the dominant direction depending on the chirality of the molecules. Dimer and superlattice formation can be explained in terms of intra- and interdimer bonds involving carboxylate, amino, and β-OH groups. The stability of the layers increases with the size of ordered islands. In racemic mixtures, we observe chiral resolution into small ordered enantiopure islands, which appears to be driven by the formation of homochiral dimer subunits and the directionality of interdimer hydrogen bonds. These islands show the same enantiospecific elongated shapes those as in low-coverage enantiopure layers.     

A new rational approximation technique based on transformational high dimensional model representation

In this work, a new rational approximation scheme, based on the recently developed Transformational High Dimensional Model Representation (THDMR) approximation method is developed. As an initial step to the construction of a rational approximation for multivariate functions via THDMR, this paper focuses on the general theoretical background of the method and gives explicit formulae for the computation of such approximants. The performance of the technique is shown by several examples both in univariate and bivariate cases.     

Health network mergers and hospital re-planning

This paper presents an integer programming formulation for the hospital re-planning problem which arises after hospital network mergers. The model finds the best re-allocation of resources among hospitals, the assignment of patients to hospitals and the service portfolio to minimize the system costs subject to quality and capacity constraints. An application in the Turkish hospital networks case is illustrated to show the implications of consolidation of health insurance funds on resource allocations and flow of patients in the system.     

Biodegradation of chemically modified wheat gluten-based natural polymer materials

Biodegradation of a series of chemically modified thermally processed wheat gluten (WG)-based natural polymers were examined according to Australian Standard (AS ISO 14855). Most of these materials reached 93-100% biodegradation within 22 days of composting, and the growth of fungi and significant phase deformation were observed during the process. Chemical crosslinking did slow down the rate or reduce the degree of the biodegradation with different behaviours for different modified systems. The segments containing structures derived from the reactions with additives such as tannin or epoxidised soybean oil remained in the degradation residues while the glycidoxypropyl trimethoxysilane agent produced ∼20% un-degraded residues containing silicon-crosslinking structures. The biodegradation rate of each component of the materials was also different with the protein and starch components degraded fast but lipid degraded relatively slowly.     

Oil recovery performances of surfactant solutions by capillary imbibition

Critical parameters playing a role in oil recovery by capillary imbibition of surfactant solutions were studied. Experiments conducted on sandstone and carbonate samples using different oil and surfactant types were evaluated for surfactant selection. In this evaluation interfacial tension (IFT), surfactant type, solubility characteristics of surfactants, rock type, initial water (pre-wet rock), and surfactant concentration were considered. In addition to these, a new technique was adopted to facilitate the surfactant screening process. This technique is based on assigning inorganic and organic property values and plotting organic conception diagrams (OCD) for surfactants. OCD defines the property of a compound in terms of physical chemistry in such a way that the property that depends much on the van der Waals force is called "organic" and the one that depends much on electric affinity is called "inorganic." Correlations between the capillary imbibition recovery performance and the properties of surfactant and oil (organic value (OV), inorganic value (IV), and IFT of surfactant solutions, oil viscosity, and surfactant type) were obtained. These correlations are expected to be useful in selecting the proper surfactant for improved oil recovery as well as identifying the effects of surfactant properties on the capillary imbibition performance.     

p-Hertz excitation spectroscopy of an optical antenna, optical transmitter-receiver mechanism

o-Xylene sensitized biacetyl fluorescence and phosphorescence have been investigated and photosensitized fluorescence and phosphorescence lifetimes of biacetyl in the vapor phase have been determined. Attempts to detect the triplet of biacetyl by its absorption spectrum were unsuccessful, primarily due to, it is believed, the low extinction coefficients of the triplet, and the low triplet concentrations produced by the optical pumping device at room temperature.