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Void Space (void + space)
Selected AbstractsPore properties as indicators of breakdown mechanisms in experimentally weathered limestonesEARTH SURFACE PROCESSES AND LANDFORMS, Issue 8 2001Dawn T. Nicholson Abstract The results are reported of four experimental weathering tests , freeze , thaw, wetting and drying, slake durability and salt weathering , on five different types of limestone. Effective porosity, mercury intrusion porosimetry and scanning electron microscopy were used to evaluate changes in pore properties, while weight loss and fracture density were used to assess deterioration severity. A primary aim was to observe modifications in porosity due to weathering and to draw inferences about the internal rock deterioration mechanisms taking place. It is concluded that the five limestones not only show a wide range of resistance to weathering in general but considerable difference in resistance to particular weathering processes. Consequently, when assessing durability it is essential to consider rock properties in the context of the weathering process to which the rock is subject. The type of deterioration indicator used is also important in interpretation of durability. A variety of pore modification mechanisms operate, including changes in pore connectivity, pore infilling, and the introduction of additional void space. There are indications that changes to the internal pore structure of rocks due to weathering may be a precursor to more substantial macrodeterioration. Copyright © 2001 John Wiley & Sons, Ltd. [source] Porous Structures: In situ Porous Structures: A Unique Polymer Erosion Mechanism in Biodegradable Dipeptide-Based Polyphosphazene and Polyester Blends Producing Matrices for Regenerative Engineering (Adv. Funct.ADVANCED FUNCTIONAL MATERIALS, Issue 17 2010Mater. Abstract Synthetic biodegradable polymers serve as temporary substrates that accommodate cell infiltration and tissue in-growth in regenerative medicine. To allow tissue in-growth and nutrient transport, traditional three-dimensional (3D) scaffolds must be prefabricated with an interconnected porous structure. Here we demonstrated for the first time a unique polymer erosion process through which polymer matrices evolve from a solid coherent film to an assemblage of microspheres with an interconnected 3D porous structure. This polymer system was developed on the highly versatile platform of polyphosphazene-polyester blends. Co-substituting a polyphosphazene backbone with both hydrophilic glycylglycine dipeptide and hydrophobic 4-phenylphenoxy group generated a polymer with strong hydrogen bonding capacity. Rapid hydrolysis of the polyester component permitted the formation of 3D void space filled with self-assembled polyphosphazene spheres. Characterization of such self-assembled porous structures revealed macropores (10,100 ,m) between spheres as well as micro- and nanopores on the sphere surface. A similar degradation pattern was confirmed in vivo using a rat subcutaneous implantation model. 12 weeks of implantation resulted in an interconnected porous structure with 82,87% porosity. Cell infiltration and collagen tissue in-growth between microspheres observed by histology confirmed the formation of an in situ 3D interconnected porous structure. It was determined that the in situ porous structure resulted from unique hydrogen bonding in the blend promoting a three-stage degradation mechanism. The robust tissue in-growth of this dynamic pore forming scaffold attests to the utility of this system as a new strategy in regenerative medicine for developing solid matrices that balance degradation with tissue formation. [source] In situ Porous Structures: A Unique Polymer Erosion Mechanism in Biodegradable Dipeptide-Based Polyphosphazene and Polyester Blends Producing Matrices for Regenerative EngineeringADVANCED FUNCTIONAL MATERIALS, Issue 17 2010Meng Deng Abstract Synthetic biodegradable polymers serve as temporary substrates that accommodate cell infiltration and tissue in-growth in regenerative medicine. To allow tissue in-growth and nutrient transport, traditional three-dimensional (3D) scaffolds must be prefabricated with an interconnected porous structure. Here a unique polymer erosion process through which polymer matrices evolve from a solid coherent film to an assemblage of microspheres with an interconnected 3D porous structure is demonstrated for the first time. This polymer system is developed on the highly versatile platform of polyphosphazene-polyester blends. Co-substituting a polyphosphazene backbone with both hydrophilic glycylglycine dipeptide and hydrophobic 4-phenylphenoxy group generates a polymer with strong hydrogen bonding capacity. Rapid hydrolysis of the polyester component permits the formation of 3D void space filled with self-assembled polyphosphazene spheres. Characterization of such self-assembled porous structures reveals macropores (10,100 ,m) between spheres as well as micro- and nanopores on the sphere surface. A similar degradation pattern is confirmed In vivo using a rat subcutaneous implantation model. 12 weeks of implantation results in an interconnected porous structure with 82,87% porosity. Cell infiltration and collagen tissue in-growth between microspheres observed by histology confirms the formation of an in situ 3D interconnected porous structure. It is determined that the in situ porous structure results from unique hydrogen bonding in the blend promoting a three-stage degradation mechanism. The robust tissue in-growth of this dynamic pore forming scaffold attests to the utility of this system as a new strategy in regenerative medicine for developing solid matrices that balance degradation with tissue formation. [source] Hollow Mesoporous Zirconia Nanocapsules for Drug DeliveryADVANCED FUNCTIONAL MATERIALS, Issue 15 2010Shaoheng Tang Abstract Hollow mesoporous zirconia nanocapsules (hm -ZrO2) with a hollow core/porous shell structure are demonstrated as effective vehicles for anti-cancer drug delivery. While the highly porous feature of the shell allows the drug, doxorubicin(DOX), to easily pass through between the inner void space and surrounding environment of the particles, the void space in the core endows the nanocapsules with high drug loading capacity. The larger the inner hollow diameter, the higher their DOX loading capacity. A loading of 102% related to the weight of hm -ZrO2 is achieved by the nanocapsules with an inner diameter of 385,nm. Due to their pH-dependent charge nature, hm -ZrO2 loaded DOX exhibit pH-dependent drug releasing kinetics. A lower pH offers a faster DOX release rate from hm -ZrO2. Such a property makes the loaded DOX easily release from the nanocapsules when up-taken by living cells. Although the flow cytometry reveals more uptake of hm -ZrO2 particles by normal cells, hm -ZrO2 loaded DOX release more drugs in cancer cells than in normal cells, leading to more cytotoxicity toward tumor cells and less cytotoxicity to healthy cells than free DOX. [source] Synthesis and Lithium Storage Properties of Co3O4 Nanosheet-Assembled Multishelled Hollow SpheresADVANCED FUNCTIONAL MATERIALS, Issue 10 2010Xi Wang Abstract Single-, double-, and triple-shelled hollow spheres assembled by Co3O4 nanosheets are successfully synthesized through a novel method. The possible formation mechanism of these novel structures was investigated using powder X-ray diffraction, scanning and transmission electron microscopies, Fourier transform IR, X-ray photoelectron spectroscopy, and thermogravimetric analysis. Both poly(vinylpyrrolidone) (PVP) soft templates and the formation of cobalt glycolate play key roles in the formation of these novel multishelled hollow structures. When tested as the anode material in lithium-ion batteries (LIBs), these multishelled microspheres exhibit excellent cycling performance, good rate capacity, and enhanced lithium storage capacity. This superior cyclic stability and capacity result from the synergetic effect of small diffusion lengths in the nanosheet building blocks and sufficient void space to buffer the volume expansion. This facile strategy may be extended to synthesize other transition metal oxide materials with hollow multishelled micro-/nanostrucutures, which may find application in sensors and catalysts due to their unique structural features. [source] A parametric study of multi-phase and multi-species transport in the cathode of PEM fuel cellsINTERNATIONAL JOURNAL OF ENERGY RESEARCH, Issue 8 2008Nada Zamel Abstract In this study, a mathematical model is developed for the cathode of PEM fuel cells, including multi-phase and multi-species transport and electrochemical reaction under the isothermal and steady-state conditions. The conservation equations for mass, momentum, species and charge are solved using the commercial software COMSOL Multiphysics. The catalyst layer is modeled as a finite domain and assumed to be composed of a uniform distribution of supported catalyst, liquid water, electrolyte and void space. The Stefan,Maxwell equation is used to model the multi-species diffusion in the gas diffusion and catalyst layers. Owing to the low relative species' velocity, Darcy's law is used to describe the transport of gas and liquid phases in the gas diffusion and catalyst layers. A serpentine flow field is considered to distribute the oxidant over the active cathode electrode surface, with pressure loss in the flow direction along the channel. The dependency of the capillary pressure on the saturation is modeled using the Leverette function and the Brooks and Corey relation. A parametric study is carried out to investigate the effects of pressure drop in the flow channel, permeability, inlet relative humidity and shoulder/channel width ratio on the performance of the cell and the transport of liquid water. An inlet relative humidity of 90 and 80% leads to the highest performance in the cathode. Owing to liquid water evaporation, the relative humidity in the catalyst layer reaches 100% with an inlet relative humidity of 90 and 80%, resulting in a high electrolyte conductivity. The electrolyte conductivity plays a significant role in determining the overall performance up to a point. Further, the catalyst layer is found to be important in controlling the water concentration in the cell. The cross-flow phenomenon is shown to enhance the removal of liquid water from the cell. Moreover, a shoulder/channel width ratio of 1:2 is found to be an optimal ratio. A decrease in the shoulder/channel ratio results in an increase in performance and an increase in cross flow. Finally, the Leverette function leads to lower liquid water saturations in the backing and catalyst layers than the Brooks and Corey relation. The overall trend, however, is similar for both functions. Copyright © 2007 John Wiley & Sons, Ltd. [source] Prediction of gas sorption kinetics for porous media using MRIAICHE JOURNAL, Issue 9 2006Matthew J. Watt-Smith Abstract Diffusion and reaction within porous media involving condensable vapors are important processes in catalysis, fuel cells, and membrane separations. In this work, 3-D maps of the spatial variation of porosity, pore size and network tortuosity within a porous solid, derived from magnetic resonance images, have been used to construct a structural model for a mesoporous catalyst pellet. Simulations of the kinetic uptake, adsorption and capillary condensation of butane vapor within the porous solid, conducted on the structural model, have successfully predicted experimental measurements of the effects of the onset of capillary condensation on mass transfer rates without the need of the various adjustable parameters prevalent in other models. These findings suggest that accurate mathematical models for both the complex void space of the porous medium, and the mass transport processes taking place within it, have been successfully developed. © 2006 American Institute of Chemical Engineers AIChE J, 2006 [source] Impact craters on small icy bodies such as icy satellites and comet nucleiMONTHLY NOTICES OF THE ROYAL ASTRONOMICAL SOCIETY, Issue 2 2005M. J. Burchell ABSTRACT Laboratory data and the results of modelling are combined to predict the possible size of craters in icy bodies such as a comet nucleus. This is done in particular for the case of a a 370-kg mass impacting a body the size of the nucleus of comet 9P/Temple-1 at 10 km s,1. This reproduces the Deep Impact comet impact to occur in 2005, when a NASA spacecraft will observe at close range an impact on the comet nucleus of an object deployed from the main spacecraft. The predicted crater size depends not only on uncertainties in extrapolation from laboratory scale and the modelling in general, but also on assumptions made about the nature of the target. In particular, allowance is made for the full range of reasonable target porosities; this can significantly affect the outcome of the Deep Impact event. The range of predicted crater sizes covers some 7,30 m crater depth and some 50,150 m crater diameter. An increasingly porous target (i.e. one with a higher percentage of void space) will increase the depth of the crater but not necessarily the diameter, leading to the possibility of an impact event where much of the crater formation is in the interior of the crater, with work going into compaction of void space and some possible lateral growth of the crater below the surface entrance. Nevertheless, for a wide range of scenarios concerning the nature of the impact, the Deep Impact event should penetrate the surface to depths of a few tens of metres, accessing the immediate subsurface regions. In parallel to this, the same extrapolation methods are used to predict the size of impactors that may have caused the features observed on the surfaces of small bodies, e.g. the Saturnian satellite Phoebe and the nucleus of comet P/Wild-2. [source] Mechanism of the first-order phase transition of an acylurea derivative: observation of intermediate stages of transformation with a detailed temperature-resolved single-crystal diffraction methodACTA CRYSTALLOGRAPHICA SECTION B, Issue 3 2003Daisuke Hashizume The process of the first-order solid-to-solid phase transition of 1-ethyl-3-(4-methylpentanoyl)urea (1) was observed by means of a detailed temperature-resolved single-crystal diffraction method, which resembles watching a series of stop-motion photographs. The transition consists of two elementary processes, one supramolecular and the other molecular. Crystal structures from before and after the phase transition are isostructural. The straight-ribbon-like one-dimensional hydrogen-bonding structure is formed and stacked to form a molecular layer. The geometry of the layer is retained during the phase transition. The relative position of the layer with its neighbours, on the other hand, changes gradually with increasing temperature. The change is accelerated at the temperature representing the start of the endotherm seen in the DSC curves of (1). The structural variation yields void space between the neighbouring layers. When the void space grows enough that the crystal is unstable, the 3-methylbutyl group on the last of the molecules turns into a disordered structure with drastic conformational changes to fill up the void space. The phase transition process is well supported with simple force-field calculations. A crystal of 1-(4-methylpentanoyl)-3-propylurea (2), which shows no solid-to-solid phase transitions, was also analysed by the same method for comparison. [source] A three-dimensional pyrazine-2,5-dicarboxylate CdII coordination framework with new (4,4,4)-connected three-nodal topologyACTA CRYSTALLOGRAPHICA SECTION C, Issue 1 2009Ping Yang Poly[(,4 -pyrazine-2,5-dicarboxylato)cadmium(II)], [Cd(C6H2N2O4)]n or [Cd(pzdc)]n (pzdc is the pyrazine-2,5-dicarboxylate dianion), has been synthesized hydrothermally. The asymmetric unit consists of a CdII atom and two independent halves of pzdc ligands that can be expanded via inversion through the centres of the ligands so that each ligand binds to four CdII atoms with the same binding mode using six donor atoms. The CdII centre is in a distorted octahedral coordination geometry with four O- and two N-atom donors from four pzdc ligands. The infinite linkage of the metal atoms and ligands forms a three-dimensional framework with a rectangular channel which is so narrow that there is no measurable void space in the overall structure. This coordination polymer represents the first example of (4,4,4)-connected three-nodal framework. [source] Organic Intercalation Material: Reversible Change in Interlayer Distances by Guest Release and Insertion in Sandwich-Type Inclusion Crystals of Cholic AcidCHEMISTRY - A EUROPEAN JOURNAL, Issue 6 2005Kazunori Nakano Dr. Abstract Cholic acid (CA) forms inclusion crystals that have a sandwich-type lamellar structure constructed by the alternative stacking of host bilayers and guest layers. Five disubstituted benzenes, o -toluidine, m -fluoroaniline, o -chlorotoluene, o -bromotoluene, and indene, are accommodated in the two-dimensional void space between the host bilayers at 1:2 host,guest stoichiometries. Thermal gravimetric analysis of the inclusion crystals revealed that all the guest molecules, except o -toluidine, are released in two separate steps, indicating the formation of intermediate crystals after the first guest release. Adequate heat treatment of the four inclusion crystals induces release of half or three quarters of the guest molecules. X-ray diffraction patterns of the intermediate crystals revealed that the crystals have a bilayer structure the same as those of the common CA inclusion crystals. They have one-dimensional cavities, in which the guest molecules are included at a 1:1 or 2:1 host,guest stoichiometry. These facts indicate that the host bilayers move 1.6,4.5 Å perpendicular to the layer direction by desorption of the guest molecules. Furthermore, a reverse structural change is also achieved by absorption of the guest molecules to regenerate the starting sandwich-type inclusion crystals. This reversible change in the host bilayer by the guest sorption and desorption is a novel example of organic intercalation materials. [source] | ||||||||||