Film morphology and reaction rate for the CVD of tungsten by the WF6—SiH4 reaction

Journal of Electronic Materials - Low pressure chemical vapor deposition (LPCVD) of tungsten (W) by SiH4 reduction of WF6 on Si(100) surfaces was studied in a single-wafer, cold-wall reactor over a...     

The mechano-sorptive behavior of flexible water-blown polyurethane foams

Samples of flexible water-blown slabstock polyurethane foams were compressed under constant load to study the effects of cycling moisture content on creep behavior and compare this behavior with the creep response where either a constant high or low moisture environment existed at the same temperature. Three sets of foams were tested: (1) 4 pph water content slabstock foam; (2) 5 pph water content slabstock foam; and (3) 2 pph water content molded foam. As the moisture conditions were cycled from low to high humidity while maintaining constant temperature in an environmental chamber, the compressive strain increased in subsequent steps with larger increases observed during the desorption portion of the humidity cycling. All three sets of foams showed similar behavior at a given temperature. At a temperature of 40°C, the strain levels under cyclic moisture conditions surpassed those levels observed at the highest constant relative humidity. During the first absorption step, the creep level increased. During any subsequent absorption step, the creep level either increased very little or none at all. Finally, during any desorption step, the creep level increased. This overall phenomenon of enhanced creep under cyclic moisture levels is attributed to water interacting with the hydrogen bonded structure within the foam. These hydrophillic interactions, principally promoted within the hard segment regions due to high hydrogen bonding, are disrupted causing slippage and increased in strain. As the foam is rapidly dired, regions of free volume are induced by the loss of water thus causing further increases in strain Prior to the reestablishment of well ordered hydrogen bonding. Further support to this proposition was given by the results obtained at a temperature of 90° C where it is well known that hydrogen bonds are much more mobile. Here, the strain levels under cyclic moisture conditions were nearly the same as those under constant high relative humidity. Weakening of the hydrogen bonds by means such as increased temperature resulted in similar strain levels to those under cyclic moisture levels. © 1993 John Wiley & Sons, Inc.     

A tabu-search based heuristic for the hub covering problem over incomplete hub networks

Hub location problems deal with finding the location of hub facilities and with the allocation of demand nodes to these located hub facilities. In this paper, we study the single allocation hub covering problem over incomplete hub networks and propose an integer programming formulation to this end. The aim of our model is to find the location of hubs, the hub links to be established between the located hubs, and the allocation of non-hub nodes to the located hub nodes such that the travel time between any origin–destination pair is within a given time bound. We present an efficient heuristic based on tabu search and test the performance of our heuristic on the CAB data set and on the Turkish network.     

Photoinduced electron transfer mechanism between green fluorescent protein molecules and metal oxide nanoparticles

Green fluorescent protein (GFP) molecules are attached to titanium dioxide and cadmium oxide nanoparticles via sol–gel method and fluorescence dynamics of such a protein–metal oxide assembly is investigated with a conventional time correlated single photon counting technique. As compared to free fluorescent protein molecules, time-resolved experiments show that the fluorescence lifetime of GFP molecules bound to these metal oxide nanoparticles gets shortened dramatically. Such a decrease in the lifetime is measured to be 22 and 43 percent for cadmium oxide and titanium dioxide respectively, which is due to photoinduced electron transfer mechanism caused by the interaction of GFP molecules (donor) and metal oxide nanoparticles (acceptor). Our results yield electron transfer rates of 3.139×10⁸ s⁻¹ and 1.182×10⁸ s⁻¹ from the GFP molecules to titanium dioxide and cadmium oxide nanoparticles, respectively. The electron transfer rates show a marked decrease with increasing driving force energy. This effect represents a clear example of the Marcus inverted region electron transfer process.     

Drying of Inorganic Particulate Compounds

ABSTRACT

Inorganic particulates are usually dried in a fixed bed, fluidized bed, or spray dryers. These compounds are easy to dry, once their physical structure, with high porosity, allows moisture content removal with low resistances. For fluidized bed of alumina particle evaluations, a laboratory-scale drying unit was built. The drying experiments were carried out with alumina particles with different diameters to evaluate temperature and air flow rate effects on drying kinetics and bed height. In another case, the dehydration of a mixture of rare-earth chlorides in a fluidized bed was studied, aiming at the production of anhydrous rare-earth chlorides, used to obtain mischmetal by electrolytic and metallothermic processes. The spray drying experiments were carried out in a pilot plant. Spray drying is a technique largely applied in industrial processes to dry solutions or suspensions, converting their solid parts into a dried powder. A set of rare-earth drying experiments was carried out, aiming at the development of techniques to obtain a powder that could satisfy international morphological requirements. The results allowed evaluating the effects of air flow rate, feed concentration, atomizer model, rotation velocity, and atomization pressure on powder density and particle size distribution.     

Effective factors improving catalyst layers of PEM fuel cell

Cathode catalyst layer has an important role on water management across the membrane electrode assembly (MEA). Effect of Pt percentage in commercial catalyst and Pt loading from the viewpoint of activity and water management on performance was investigated. Physical and electrochemical characteristics of conventional and hydrophobic catalyst layers were compared. Performance results revealed that power density of conventional catalyst layers (CLs) increased from 0.28 to 0.64 W/cm² at 0.45 V with the increase in Pt amount in commercial catalyst from 20% to 70% Pt/C for H₂/Air feed. In the case of H₂/O₂ feed, power density of CLs increased from 0.64 to 1.29 W/cm² at 0.45 V for conventional catalyst layers prepared with Tanaka. Increasing Pt load from 0.4 to 1.2 mg/cm², improved kinetic activity at low current density region in both feeding conditions. Scattering electron microscopy (SEM) images revealed that thickness of the catalyst layers (CLs) increases by increasing Pt load. Electrochemical impedance spectroscopy (EIS) results revealed that thinner CLs have lower charge transfer resistance than thicker CLs. Inclusion of 30 wt % Polytetrafluoroethylene (PTFE) nanoparticles in catalyst ink enhanced cell performance for the electrodes manufactured with 20% Pt/C at higher current densities. However, in the case of 70% Pt/C, performance enhancement was not observed. Cyclic voltammetry (CV) results revealed that 20% Pt/C had higher (77 m²/g) electrochemical surface area (ESA) than 70% Pt/C (65 m²/g). In terms of hydrophobic powders, ESA of 30PTFE prepared with 70% Pt/C was higher than 30PTFE prepared with 20 %Pt/C. X-Ray Diffractometer (XRD) results showed that diameter of Pt particles of 20% Pt/C was 2.5 nm, whereas, it was 3.5 nm for 70% Pt/C, which confirms CV results. Nitrogen physisorption results revealed that primary pores of hydrophobic catalyst powder prepared with 70% Pt/C was almost filled (99%) with Nafion and PTFE.     

High performance water-borne paints with high volume solids based on bimodal latexes

The performance of water-borne paints formulated with five different high solids content acrylic (MMA/BA/MAA) latexes was investigated. These latexes had different particle size distributions (unimodal at 61 wt% and bimodal with the large mode below or above 350 nm at 65 wt% solids), different types of surfactant and in one case the carboxylic monomer was omitted.     

Metal complexation of thiacrown ether macrocycles by electrospray ionization mass spectrometry

In the present study, electrospray ionization mass spectrometry is used to evaluate the metal-binding selectivities of an array of novel caged macrocycles for mercury(II), lead(II), cadmium(II), and zinc(II) ions. In homogeneous methanol/chloroform solutions as well as extractions of metals from aqueous solution by macrocycles in chloroform, it is found that the type of heteroatom (S, O, N), cavity size, and presence of other substituents influence the metal selectivities. Several of the macrocycles in this study bind mercury ion very selectively and efficiently in the presence of many other metal ions and have an avidity toward mercury that was tunable by the size and combination of heteroatoms in the macrocycle ring and the number of cage groups attached. The extraction mechanism was further investigated by determining the variation in extraction selectivity as a function of the counterions of the mercury salts.