Internal Surface Area (internal + surface_area)

Distribution by Scientific Domains


Selected Abstracts


Organic Ligands Made Porous: Magnetic and Catalytic Properties of Transition Metals Coordinated to the Surfaces of Mesoporous Organosilica

ADVANCED FUNCTIONAL MATERIALS, Issue 7 2010
Andreas Kuschel
Abstract Inorganic solids with porosity on the mesoscale possess a high internal surface area and a well-accessible pore system. Therefore, it is a relevant task to equip the surfaces of such materials with a maximum density of various organic functional groups. Among these functions it is the capability of coordinating to metal species as a ligand that is of extraordinary importance in many areas, for example, in catalysis. This paper describes how prominent ligands containing donor functions such as carboxylic, thio, chelating, or amine groups can be obtained in the form of nanoporous organosilica materials. The coordination of metal centers such as CoII, MnII, VIV, or PtIV is studied in detail. The magnetic properties of the corresponding materials and some applications in catalysis are reported. A quantitative determination of the surface density of donor atoms by distance measurements using EPR spectroscopy is shown. [source]


Polydisperse Spindle-Shaped ZnO Particles with Their Packing Micropores in the Photoanode for Highly Efficient Quasi-Solid Dye-Sensitized Solar Cells

ADVANCED FUNCTIONAL MATERIALS, Issue 3 2010
Yantao Shi
Abstract In this paper, a novel hierarchically structured ZnO photoanode for use in quasi-solid state dye-sensitized solar cells (DSCs) is presented. The film is composed of polydisperse spindle-shaped ZnO particles that are prepared through direct precipitation of zinc acetate in aqueous solution. Without additional pore-forming agents, the microporous structure is well constructed through the packing of polydisperse ZnO particles. In the film, small ZnO particles are able to improve interparticle connectivity and offer a large internal surface area for sufficient dye-adsorption; on the other hand, particles of larger size can enhance the occurrence of light-scattering and introduce micropores for the permeation of quasi-solid state electrolytes. Meanwhile, morphologies, particle size, and specific areas of the products are controlled by altering the reactant concentration and synthetic temperature. Combined with a highly viscous polymer gel electrolyte, a device based on this ZnO photoanode shows high conversion efficiencies, 4.0% and 7.0%, under 100 and 30,mW cm,2 illumination, respectively. Finally, the unsealed device is demonstrated to remain above 90% of its initial conversion efficiency after 7 days, showing excellent stability. [source]


Modeling and experimental studies on combustion characteristics of porous coal char: Volume reaction model

INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 5 2010
Anup Kumar Sadhukhan
A generalized single-particle model for the prediction of combustion dynamics of a porous coal char in a fluidized bed is analyzed in the present work using a volume reaction model (VRM). A fully transient nonisothermal model involving both heterogeneous and homogeneous chemical reactions, multicomponent mass transfer, heat transfer with intraparticle resistances, as well as char structure evolution is developed. The model takes into account convection and diffusion inside the particle pores, as well as in the boundary layer. By addressing the Stefan flow originated due to nonequimolar mass transfer and chemical reactions, this work enables a more realistic analysis of the combustion process. The model, characterized by a set of partial differential equations coupled with nonlinear boundary conditions, is solved numerically using the implicit finite volume method (FVM) with a FORTRAN code developed in-house. The use of a FVM for solving such an elaborate char combustion model, based on the VRM, was not reported earlier. Experiments consisting of fluidized-bed combustion of a single char particle were carried out to determine the internal surface area of a partially burned char particle and to enable model validation. Predicted results are found to compare well with the reported experimental results for porous coal char combustion. The effects of various parameters (i.e., bulk temperature and initial particle radius) are examined on the dynamics of combustion of coal char. The phenomena of ignition and extinction are also investigated. © 2010 Wiley Periodicals, Inc. Int J Chem Kinet 42: 299,315, 2010 [source]


Thermal machines based on surface energy of wetting: Thermodynamic analysis

AICHE JOURNAL, Issue 3 2003
A. Laouir
This work proposes an original thermodynamic-energetic analysis of the feasibility and ideal performance of thermal machines based on the wetting phenomenon proposed by V. A. Eroshenko. The extension or contraction of a liquid film is taken as a "tutorial" example to introduce the basic thermodynamic relations of this 2-D transformation. It implies both mechanical and thermal effects, and this coupling allows conversion of heat to work (thermal engine) or conversely to pump heat (refrigeration/heat pump effect). A similar approach is then developed for the interface between a liquid and a highly microporous solid, having a large internal surface area. The thermodynamic behavior of this interface involves as state variables the surface tension of the liquid, the contact angle, and their dependence on temperature. Depending on the relative magnitude and sign of these quantities, and, therefore, on the working couple and the temperature range, a variety of machine cycles are feasible, or excluded, and a method is proposed for a comprehensive inventory. Order-of-magnitude calculations of the energy densities are presented based on the existing experimental data for several systems involving water as the fluid. The tentative conclusions are that the energy densities are very small on a mass basis compared to conventional systems based on vaporization, but the contrary is true on a volume basis because the phase transformation (extension of the surface) occurs in a condensed state. There may, therefore, be some niches for thermal machines of this type, but they remain to be identified and validated. [source]


Depth-Resolved Porosity Investigation of EB-PVD Thermal Barrier Coatings Using High-Energy X-rays

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2004
Anand A. Kulkarni
Demands for designing prime reliant, energy-efficient, and high-performance thermal barrier coatings (TBCs) in gas turbines have led to a growing interest toward comprehensive microstructural characterization. Here we investigate the novel use of high-energy X-rays for small-angle X-ray scattering (SAXS), together with wide-angle scattering and radiography, for the depth-resolved characterization of TBCs grown by electron beam physical vapor deposition (EB-PVD). The coating microstructure is found to consist of columns perpendicular to the substrate, extending through the thickness, with a [001] growth texture and significant intercolumnar porosity. In addition, overshadowing effects during deposition together with gas entrapment give rise to nanoscale intracolumnar porosity consisting of featherlike and globular pores. Radiography showed an increase in the total porosity, from 15% near the substrate to 25% near the coating surface, which is ascribed to an increase in the intercolumnar spacing at the top of the coating. By contrast, the small-angle scattering studies, which are sensitive to fine features, showed the pore internal surface area to be greatest near the substrate. [source]


Structure and dynamics of silica-filled polymers by SANS and coherent SAXS

MACROMOLECULAR SYMPOSIA, Issue 1 2002
Erik Geissler
Random crosslinking in elastomers gives birth to local variations in the crosslink density. When the network is swollen in a low-molecular-weight solvent, competition between the osmotic pressure and the local elastic constraints transforms these variations into differences in polymer concentration, the range and amplitude of which can be measured by small-angle X-ray or neutron scattering (SAXS or SANS). In filled systems, the distribution both of the polymer and of the elastic constraints is modified. By varying the proportion of deuterated solvent in the network, the scattering function of the polymer can be distinguished from that of the filler using SANS. Such measurements yield not only the internal surface area of the filler particles but also the fraction of that surface in contact with the polymer. The recently developed technique of quasi-elastic SAXS detects slow dynamic processes at wave vectors larger than those accessible with visible light lasers. This technique is used to investigate the dynamics of filler particles in uncrosslinked polymer melts. It is directly shown that the structural reorganization process of the filler following an external mechanical perturbation is diffusion-controlled. [source]


Gravimetric method to find internal surface of macroporous silicon membranes

PHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 6 2007
A. A. Nechitailov
Abstract A simple method to evaluate the internal surface area, porosity, pore diameter and pore density of macroporous silicon membranes has been proposed and tested. The porosity p is obtained from the mass loss under anodizing, and the surface area per unit volume Sv is determined from the mass of SiO2 formed on the pore surface as a result of thermal oxidation. The average pore diameter d and pore density N can be easily calculated from the obtained Sv and p. Experimental verification of d and N was performed by means of SEM and optical microscope images; Sv was checked by BET technique. Surface area and porosity on the resistivity of initial n-Si in the range , = 3,25 Ohm · cm have been studied for the samples with regular and self-organized macropore "lattices". The obtained values are within the limits p = 27,50%, Sv = 2800,6000 cm2/cm3, d = 1.9,6.5 ,m, N = 1.4,10 × 106 cm,2, and in a good agreement with the data of microscopic characterization. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source]


Immunoaffinity removal of xenoreactive antibodies using modified dialysis or microfiltration membranes

BIOTECHNOLOGY & BIOENGINEERING, Issue 2 2003
Sujatha Karoor
Abstract Hyperacute rejection following xenogeneic transplantation in primates is mediated by naturally occurring IgM antibodies, which are specifically directed to ,-Galactosyl residues on many nonprimate mammalian cells. Current approaches to remove these anti-,Gal IgM include plasmapheresis followed by immunoaffinity adsorption on bead columns using synthetic Gal epitopes, which requires two pieces of complex equipment. In this study, we explored the use of immunoaffinity adsorption with hollow fiber microporous or dialysis membranes to which a synthetic ,Gal trisaccharide ligand is bound. Covalent attachment of ligand directly to the surface produced negligible binding, but use of long-chain polyamines as reactive spacers yielded binding densities for anti-,Gal IgM as high as 89 mg/mL membrane volume in breakthrough curve experiments with microporous nylon membranes having an internal surface area of 4.2 m2/mL membrane volume. A crossflow microfilter fabricated from the membranes described in this study and having about 0.4 m2 luminal surface area would be able to carry out plasma separation and immunoadsorption in a single device with a large excess of binding capacity to ensure that all plasma that filters across the device and is returned to a human patient is essentially free of anti-,Gal IgM. We conclude that immunoaffinity removal of xenoreactive antibodies using microfiltration hollow fiber membranes is feasible and has potential advantages of efficiency and simplicity for clinical application. © 2002 Wiley Periodicals, Inc. Biotechnol Bioeng 81: 134,148, 2003. [source]