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Effect of embedded metal compound on porosity of silica colloids prepared by spray reaction of silicon tetrachloride.

Attempts to prepare macroporous silica particles and metal-compound-nanoparticle-embedded silica microspheres were carried out using reactions between silicon tetrachloride and ultrasonic generating microdroplets including metal (Na, K, Al, Ni, Ti, Pt) compounds. Samples were collected by dry and wet processes. In the case of using nickel and aluminum compounds, acid-treated samples were also prepared. The obtained samples were characterized by scanning electron microscopy, X-ray fluorescence spectroscopy, powder X-ray diffractometry, mercury porosimetry, and the nitrogen adsorption method. The macroporous silica particles were prepared by removing the salt crystals, such as NaCl and KCl, formed in the silica frame. For acid-resistant metals, platinum- and titanium-compound nanoparticles are easily embedded in silica microspheres using these metal-compound solutions. For acid-soluble metals, aluminum- and nickel-compound-nanoparticle-embedded silicas were prepared by applying neutralization of the collection water. Micropores and mesopores were produced in wet-process samples. Acid treatment induced the increase of micropore volumes.

Journal Article↗

TiO2 anatase-based membranes with hierarchical porosity and photocatalytic properties.

Taking benefit of previously obtained results, stable complex organic-inorganic hybrid suspensions are successfully prepared by mixing a polystyrene latex aqueous suspension, a titania hydrosol and a nonionic triblock copolymer. These suspensions can be then deposited as thin films on dense or porous substrates. Solvent evaporation induces the formation of spherical micelles by self-assembly of the amphiphilic molecules during the drying of the films. Two types of isolated spherical macropores (few ten nanometers) and mesopores (4-5 nm) are generated inside the layers by the thermal removal of the polystyrene particles and of the micelles, respectively. The remaining inorganic network exhibits an additional interconnected microporosity with a mean pore size of 1.5 nm, resulting from the aggregation of the anatase nanoparticles. A complete removal of the templating units at low temperature is possible using the photocatalytic properties of the anatase network. Such layers exhibit attractive properties for the design of ceramic membranes. They can be advantageously used in order to increase the permeability of the separative layer and to reduce the number of intermediate layers of these asymmetric structures.

Journal Article↗

Fast method for simulation of radionuclide chain migration in dual porosity fracture rocks.

In fractured rocks with a porous rock matrix such as granites, radionuclides will flow with the water in the fracture network. The nuclides will diffuse in and out the rock matrix where they can sorb and be considerably retarded compared to the water velocity. A water parcel entering the network will mix and split at the fracture intersections and parts of the original parcel will traverse a multitude of different fractures. The flowrates, velocities, sizes and apertures of the fractures can vary widely. Normally one must solve the transport equations for every fracture and use the effluent concentration as inlet condition to the next fracture and so on. It is shown that under some weakly simplified conditions it suffices to determine one single parameter group containing information on the flow wetted surface that a water parcel contacts along the entire path. It is also shown how this can be obtained. Then, solving the transport equations only once for time and location along the path gives the concentration and nuclide flux of every nuclide in the chain everywhere along a path. The same solution actually is valid for every path in the network. This dramatically reduces the computation effort. The same approach can be used for models based on streamtubes.

Computational Biology↗

Study of porosity and stiffness measurement of nanoporous aerogel films with wideband ultrasonic surface waves.

Nanoporous aerogel films are of great scientific and commercial interest because of their outstanding potential for application to microelectronic interconnect, associated with low dielectric constant. Of the parameters which describe such aerogel films, density/porosity and stiffness are two of the most critical, but are difficult to measure. This paper shows how measurement of the dispersion of laser-generated surface acoustic wavepackets travelling on submicron-thick aerogel films on silicon substrates allows the density and Young's modulus to be extracted reliably. Particular attention is paid to accuracy of measurements and sensitivity to input data; and a method for extracting measurements on very thin films (<300 nm) is presented.

Journal Article↗

Comparison and optimization of three centrifugation systems for reducing porosity of Simplex P bone cement.

Simplex P bone cement was spun for 30, 60, and 120 seconds in three different centrifugation systems (I.E.C. HN-S II, I.E.C. clinical, and Johnson & Johnson) to determine whether differences among the three systems also produce differences in the improvement of the fatigue strength of the cement. The fatigue properties of the cement after centrifugation were also assessed when it was mixed with monomer that had been chilled to 0 degrees C. There were important and statistically significant differences in the fatigue life of Simplex P spun for the same duration in the different centrifuges. Simplex P prepared as recommended by the manufacturer had an average fatigue life of 15,143 cycles in the test system used. Optimum centrifugation among the techniques studied increased the fatigue life nearly fivefold, to the range of 71,000 cycles. Taking into account both the fatigue strength and the viscosity of the cement, the optimum centrifugation system for improving the fatigue life of Simplex P bone cement is the Miller cartridge containing two packs of cement spun in the IEC-HN-S II centrifuge. The authors recommend 30 seconds of centrifugation if the monomer is not chilled prior to mixing and 60 seconds if the monomer is chilled.

Bone Cements↗

Optimization of the geometry and porosity of microelectrode arrays for sensor design.

This paper describes the systematic investigation of a range of microelectrode arrays with varying dimensions fabricated by standard photolithographic and reactive-ion etching techniques. As expected from theory, the electrochemical behavior of microelectrode arrays with a constant individual diameter varied strongly with center-to-center spacing, the larger the spacing the more sigmoidal the recorded voltammogram. Furthermore, the behavior of arrays with a constant relative center-to-center spacing is shown to vary with individual electrode diameter, the arrays with the smallest electrodes producing strongly peaked voltammograms. Peak current densities and signal-to-noise ratios were also obtained for a variety of array geometries, and the use of electrodeposited platinum black electrodes was investigated. To demonstrate one advantage of using a loosely packed microelectrode array in electroanalysis, a ferrocene-mediated enzyme-linked assay involving the biocatalytic reduction of H2O2 was investigated. Results showed an improved temporal response, with current-time transients reaching a steady-state response more quickly using arrays with increased center-center spacings.

Biosensing Techniques↗

Construction of a thread coater and use of azocasein release To characterize the sealant coat porosity of fibers coated with latex biocatalytic coatings

A single-stage annular fiber coating method with co-current dry-air drying at 30 degrees C has been developed for multilayer coating of 128 &mgr;m diameter polyester thread (yarn) with latex films as a model for enzyme immobilization and development of a filament biocatalytic filter. Acrylic vinyl acetate polymer coatings were sequentially metered onto the fibers by the combination of a flexible squeegee and a red rubber annulus. The thread coater can operate over a range of 0.07-1.37 m/min thread velocities while delivering a nearly constant and reproducible polymer loading of 30. 8 +/- 1.3 mg/m. A 100% polyester, 278.9 denier thread was precoated with latex to generate an approximately 369 denier sealed filament. The filament was then coated with a latex + sulfanilamide-azocasein mixture and sealed with a polymer top coat. The permeability of the polymer sealant top coat was characterized using entrapped azocasein as a tracer molecule and monitoring the azocasein release upon rehydration of the coated threads. Azocasein release rate decreased with curing time at 30 degrees C until 2 days and was invariant after 2-3 days of curing. A 282 mOsm rehydrating solution was sufficient to suppress increased azocasein release due to top coat blistering. No enhancement in the permeability of the top coat was observed when high molecular weight water soluble polymers (WSPs) were used as fillers. This probably results from the low WSP to latex ratio used (0.05-0.1) and the slow rate of WSP leaching compared to the release of azocasein. A method using 60-120 mesh silica was also developed to study the effect of mechanical abrasion of the coated threads as measured by azocasein release kinetics.

Journal Article↗

New porphyrin-based metal-organic framework with high porosity: 2-D infinite 22.2-A square-grid coordination network.

A new 2-D coordination network with 22.2-A square-grid coordination networks was prepared from a dicopper(II) tetraacetate [Cu2(AcO)4] as a linear linker motif and 5,10,15,20-tetra-4-pyridyl-21H,23H-porphine (H2TPyP) as a four-connected vertex, forming a regular high-porous structure. The characterization by N2 adsorption indicated that this coordination network has uniform micropores and gas adsorption cavities.

Journal Article↗

Layered cobalt hydroxysulfates with both rigid and flexible organic pillars: synthesis, structure, porosity, and cooperative magnetism.

The synthesis and characterization of two members of a family of porous magnetic materials is described. The structures of Co4(SO4)(OH)6(C2N2H8)0.5*3H2O and Co4(SO4)(OH)6(C6N2H12)0.5*H2O and their thermal stability can be tailored via the choice of organic pillar. The interactions between the pillaring agent and the compositionally complex inorganic layer are discussed. The influences of two pillaring agents i.e., the flexible ethylenediamine and the relatively rigid 1,4-diazabicyclo[2,2,2]octane, on thermal stability, rigidity upon guest loss, and magnetic behavior of the pillared solids are compared. The magnetism of the pillared layered cobalt hydroxides is complex due to the influences of multiple metal sites, inter- and intralayer exchange, spin-orbit coupling, and geometrical frustration. The wide variety of potential pillars, oxyanions, and possible metal substitutions at the octahedral and tetrahedral sites offers the possibility of tailoring the magnetic and porous properties of these materials.

Journal Article↗