Fuzzy α-discounting method for multi-criteria decision-making

The α-Discounting Method was developed to be an alternative to and extension of the Analytical Hierarchy Process (AHP) to solve multi-criteria decision-making (MCDM) problems with non-commensurable and conflicting criteria. In contrast to the AHP, this method works not only for pairwise comparisons but also for n-wise comparisons if relative importance of criteria can be expressed in a system of linear homogenous equations. This method also has a comparative advantage as it can transform those MCDM problems, classified as inconsistent by the AHP, into a consistent form. This study briefly compares the two methods and then develops the Fuzzy α-Discounting Method for Multi-Criteria Decision Making (Fα-DM MCDM). Two illustrative fuzzy MCDM problems from the literature have been solved to show how the Fα-DM MCDM works.     

Influence of hydrogen on thermally induced phase separation in GeO/SiO2 multilayers

The influence of the annealing atmosphere on the temperature induced phase separation of Ge oxide in GeO(x)/SiO(2) multilayers (x≈1), leading to size controlled growth of Ge nanocrystals, is explored by means of x-ray absorption spectroscopy at the Ge K-edge. Ge sub-oxides contained in the as-deposited multilayers diminish with increasing annealing temperature, showing complete phase separation at approximately 450?°C using inert N(2) ambient. The use of reducing H(2) in the annealing atmosphere influences the phase separation even at an early stage of the disproportionation. In particular, the temperature regime where the phase separation occurs is lowered by at least 50?°C. At temperatures above 400?°C the sublayer composition, and thus the density of the Ge nanocrystals, can be altered by making use of the reduction of GeO(2) by H(2).     

Optical and structural properties of zinc oxide films with different thicknesses prepared by successive ionic layer adsorption and reaction method

In this work, zinc oxide semiconducting films belonging to the II-VI group have been produced by successive ionic layer adsorption and reaction (SILAR) method on glass substrates with 10, 15, 20 and 25 cycles at room temperature. Following the deposition, the samples were dried in air at 400 °C for 1 h. The films were characterized by X-ray diffraction, field emission scanning electron microscopy and optical absorption measurement techniques. The X-ray diffractions of the films showed that they are hexagonal in structure. The crystallite size of ZnO films varied between 34 and 38 nm accordingly with the number of SILAR cycles. The material has exhibited direct band gap transition with the band gap values lying in the range between 3.13 and 3.18 eV. The red shift is observed in the absorption edge as the cycles increased. Transmission of the films decreased from 65 to 40% with increasing the number of cycles.     

Enzyme immobilization in a photosensitive conducting polymer bearing azobenzene in the main chain

A new photosensitive and thermosensitive monomer, namely bis(4-(3-thienyl ethylene)-oxycarbonyl)diazobenzene (TDAZO), was synthesized. The photochemical and thermal cis–trans isomerization of the monomer has been investigated. The rate constants of the photoisomerization of TDAZO in ACN and DCM were 0.195 and 0.308 min^?1, respectively. For spectroelectrochemical investigation and enzyme immobilization application, TDAZO copolymerized with thiophene and pyrrole. Electrochemical and spectroelectrochemical properties of P(TDAZO-co-Th) were investigated and invertase was immobilized in P(TDAZO-co-Py) copolymer. Immobilization of enzymes was carried out by the entrapment of the enzyme in conducting polymer matrices during electrochemical polymerization of pyrrole through thiophene moieties of the TDAZO. Optimum conditions for this electrode, such as pH, temperature, kinetic parameters (K _m and V _max) and operational stability were investigated. Kinetic parameters invertase-immobilized in copolymer were smaller than free enzyme. The optimum operational temperature was 10 °C higher for immobilized enzyme than that of the free enzyme. Due to strong interaction between enzyme and diazo group in the polymer main chain, thermal, pH and operational stability of enzyme has been enhanced.     

Mode I and mode II fracture toughness of E-glass non-crimp fabric/carbon nanotube (CNT) modified polymer based composites

In this study, mode I and mode II interlaminar fracture toughness, and interlaminar shear strength of E-glass non-crimp fabric/carbon nanotube modified polymer matrix composites were investigated. The matrix resin containing 0.1 wt.% of amino functionalized multi walled carbon nanotubes were prepared, utilizing the 3-roll milling technique. Composite laminates were manufactured via vacuum assisted resin transfer molding process. Carbon nanotube modified laminates were found to exhibit 8% and 11% higher mode II interlaminar fracture toughness and interlaminar shear strength values, respectively, as compared to the base laminates. However, no significant improvement was observed for mode I interlaminar fracture toughness values. Furthermore, Optical microscopy and scanning electron microscopy were utilized to monitor the distribution of carbon nanotubes within the composite microstructure and to examine the fracture surfaces of the failed specimens, respectively.     

Kinetics of swelling assisted grafting of 4-vinyl pyridine onto poly(ethylene terephthalate) fibers using a benzoyl peroxide initiator

Summary Poly(ethylene terephthalate) (PET) fibers were grafted with 4-vinyl pyridine (4-VP) using benzoyl peroxide (Bz₂O₂) as initiator. Fibers were swelled in dichloroethane (DCE) for 2 h at 90 °C to promote the incorporation and the subsequent polymerization of 4-VP onto PET fibers. Variations of graft yield with time, temperature, initiator and monomer concentrations were investigated. Percent grafting was enhanced significantly by increasing Bz₂O₂ concentration up to 2 × 1 0 ^-3 mol/L and then decreased upon further increase in initiator concentration. Increasing the 4-VP concentration up to 0.6 mol/L improves the graft yield significantly. The optimum temperature and polymerization time was found to be 50 °C and 2 h respectively. Further changes in properties of grafted PET fibers such as moisture absorption capacity and intrinsic viscosity were determined. Grafted PET fibers were charactarized by thermogravimetric analysis and scanning electron microscopy (SEM). Molar mass of the grafted chains was also determined.     

Parallel eigenvalue calculation based on multiple shift–invert Lanczos and contour integral based spectral projection method

We discuss the possibility of using multiple shift–invert Lanczos and contour integral based spectral projection method to compute a relatively large number of eigenvalues of a large sparse and symmetric matrix on distributed memory parallel computers. The key to achieving high parallel efficiency in this type of computation is to divide the spectrum into several intervals in a way that leads to optimal use of computational resources. We discuss strategies for dividing the spectrum. Our strategies make use of an eigenvalue distribution profile that can be estimated through inertial counts and cubic spline fitting. Parallel sparse direct methods are used in both approaches. We use a simple cost model that describes the cost of computing k eigenvalues within a single interval in terms of the asymptotic cost of sparse matrix factorization and triangular substitutions. Several computational experiments are performed to demonstrate the effect of different spectrum division strategies on the overall performance of both multiple shift–invert Lanczos and the contour integral based method. We also show the parallel scalability of both approaches in the strong and weak scaling sense. In addition, we compare the performance of multiple shift–invert Lanczos and the contour integral based spectral projection method on a set of problems from density functional theory (DFT).     

The effects of growth conditions on the surface properties and photocatalytic activities of anatase TiO<Subscript>2</Subscript> films prepared via electrochemical anodizing and annealing methods

In the present work, nanostructured TiO₂ films were prepared by electrochemical anodization process of titanium in fluoride-containing electrolytes using an innovative approach. After anodization, the TiO₂ films were annealed at 480?°C for 2 h in air in order to acquire anatase phase transformation and increase its crystallinity. The effects of anodization voltage, electrolyte concentration and anodization time on the formation of TiO₂ films and the photocatalytic degradation of methylene blue (MB) were discussed in details. The phase structure and surface morphology of the samples characterized by means of X-ray diffraction and scanning electron microscope. The as-prepared nanostructured TiO₂ film anodized in 0.5% HF electrolyte at 15 V for 240 min showed excellent photocatalytic degradation of MB and is promising for environmental purification.