Pore Size Distribution (pore + size_distribution)

Distribution by Scientific Domains
Distribution within Chemistry

Kinds of Pore Size Distribution

  • bimodal pore size distribution
  • narrow pore size distribution


  • Selected Abstracts


    Patterns of damage in igneous and sedimentary rocks under conditions simulating sea-salt weathering

    EARTH SURFACE PROCESSES AND LANDFORMS, Issue 1 2003
    C. Cardell
    Abstract A saline-spray artificial ageing test was used to simulate the effects produced in granites and sedimentary rocks (calcarenites, micrites and breccia) under conditions in coastal environments. Three main points were addressed in this study: the durability of the different kinds of rock to salt decay, the resulting weathering forms and the rock properties involved in the weathering processes. For this, mineralogical and textural characterization of each of the different rocks was carried out before and after the test. The soluble salt content at different depths from the exposed surfaces was also determined. Two different weathering mechanisms were observed in the granite and calcareous rocks. Physical processes were involved in the weathering of granite samples, whereas dissolution of calcite was also involved in the deterioration of the calcareous rocks. We also showed that microstructural characteristics (e.g. pore size distribution), play a key role in salt damage, because of their influence on saline solution transport and on the pressures developed within rocks during crystallization. Copyright © 2003 John Wiley & Sons, Ltd. [source]


    Capillary electrochromatography with monolithic silica column:,I.

    ELECTROPHORESIS, Issue 3 2003
    Preparation of silica monoliths having surface-bound octadecyl moieties, applications to the separation of neutral, charged species, their chromatographic characterization
    Abstract Monolithic silica columns with surface-bound octadecyl (C18) moieties have been prepared by a sol-gel process in 100 ,m ID fused-silica capillaries for reversed-phase capillary electrochromatography of neutral and charged species. The reaction conditions for the preparation of the C18-silica monoliths were optimized for maximum surface coverage with octadecyl moieties in order to maximize retention and selectivity toward neutral and charged solutes with a sufficiently strong electroosmotic flow (>,2 mm/s) to yield rapid analysis time. Furthermore, the effect of the pore-tailoring process on the silica monoliths was performed over a wide range of treatment time with 0.010 M ammonium hydroxide solution in order to determine the optimum time and conditions that yield mesopores of narrow pore size distribution that result in high separation efficiency. Under optimum column fabrication conditions and optimum mobile phase composition and flow velocity, the average separation efficiency reached 160,000 plates/m, a value comparable to that obtained on columns packed with 3 ,m C18-silica particles with the advantages of high permeability and virtually no bubble formation. The optimized monolithic C18-silica columns were evaluated for their retention properties toward neutral and charged analytes over a wide range of mobile phase compositions. A series of dimensionless retention parameters were evaluated and correlated to solute polarity and electromigration property. A dimensionless mobility modulus was introduced to describe charged solute migration and interaction behavior with the monolithic C18-silica in a counterflow regime during capillary electrochromatography (CEC )separations. The mobility moduli correlated well with the solute hydrophobic character and its charge-to-mass ratio. [source]


    Thermally Stable Nanocrystalline Mesoporous Gallium Oxide Phases

    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 22 2009
    Chinmay A. Deshmane
    Abstract Semicrystalline and fully crystalline mesoporous galliumoxide phases were synthesized in the presence of ionic and non-ionic structure directing agents via Evaporation-Induced Self-Assembly (EISA) and Self-Assembly Hydrothermal-Assisted (SAHA) methods respectively. EISA led to partially crystalline mesoporous gallium oxide phases displaying unimodal pore size distribution in the range of ca. 2,5 nm and surface areas as high as 300 m2/g. SAHA led to nanocrystalline mesoporous uniform micron-sized gallium oxide spheres (ca. 0.3,6.5 ,m) with narrow size distribution displaying cubic spinel type structure. These mesophases displayed surface areas as high as ca. 221 m2/g and unimodal pore size distribution in the 5,15 nm range. Textural properties such as surface areas and pore sizes were effectively fine-tuned by the nature and relative concentration of the structure directing agents. Due to their high surface areas, tunability of pore sizes and the nature of the wall structure, these gallium oxide mesophases could find potential applications as heterogeneous catalysts.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source]


    Microstructures: Facile Fabrication of Monolithic 3D Porous Silica Microstructures and a Microfluidic System Embedded with the Microstructure (Adv. Funct.

    ADVANCED FUNCTIONAL MATERIALS, Issue 9 2010
    Mater.
    D.-P. Kim and co-workers present the fabrication of monolithic 3D porous silica structures into a multilayer framework with bimodal pore size distribution on page 1473. The structure becomes monolithic upon pyrolyzing the stacked layers, and then easily embedded in microchannel with the aid of photolithography, leading to a microfluidic system with built-in microstructure in a site- and shape-controlled manner. [source]


    Facile Fabrication of Monolithic 3D Porous Silica Microstructures and a Microfluidic System Embedded with the Microstructure

    ADVANCED FUNCTIONAL MATERIALS, Issue 9 2010
    ZuoYi Xiao
    Abstract Monolithic 3D porous silica structures are fabricated into a multilayer framework with a bimodal pore size distribution in the micrometer and sub-micrometer range. The fabrication , which involves directed assembly of colloidal spheres, transfer printing, and removal of a sacrificial template , yields robust and mechanically stable structures over a large area. The structure becomes monolithic upon pyrolyzing the stacked layers, which induces necking of the particles. The monolithic microstructures can easily be embedded in microchannels with the aid of photolithography, leading to the formation of a microfluidic system with a built-in microstructure in a site- and shape-controlled manner. Utilization of the system results in a fourfold increase in the mixing efficiency in the microchannel. [source]


    Study of the Catalytic Layer in Polybenzimidazole-based High Temperature PEMFC: Effect of Platinum Content on the Carbon Support

    FUEL CELLS, Issue 2 2010
    J. Lobato
    Abstract In this work, the effect of platinum percentage on the carbon support of commercial catalyst for electrodes to be used in a Polybenzimidazole (PBI)-based PEMFC has been studied. Three percentages were studied (20, 40 and 60%). In all cases, the same quantity of PBI in the catalyst layer was added, which is required as a ,binder'. From Hg porosimetry analyses, pore size distribution, porosity, mean pore size and tortuosity of all electrodes were obtained. The amount of mesopores gets larger as the platinum percentage in the catalytic layer decreases, which reduces the overall porosity and the mean pore size and increases the tortuosity. The electrochemical characterisation was performed by voltamperometric studies, assessing the effective electrochemical surface area (ESA) of the electrodes, by impedance spectroscopy (IS), determining the polarisation resistance, and by the corresponding fuel cell measurements. The best results were obtained for the electrodes with a content of 40% Pt on carbon, as a result of an adequate combination of catalytic activity and mass transfer characteristics of the electrode. It has been demonstrated that the temperature favours the fuel cell performance, and the humidification does not have remarkable effects on the performance of a PBI-based polymer electrolyte membrane fuel cell (PEMFC). [source]


    Wettability alteration of caprock minerals by carbon dioxide

    GEOFLUIDS (ELECTRONIC), Issue 2 2007
    P. CHIQUET
    Abstract One of the critical factors that control the efficiency of CO2 geological storage process in aquifers and hydrocarbon reservoirs is the capillary-sealing potential of the caprock. This potential can be expressed in terms of the maximum reservoir overpressure that the brine-saturated caprock can sustain, i.e. of the CO2 capillary entry pressure. It is controlled by the brine/CO2 interfacial tension, the water-wettability of caprock minerals, and the pore size distribution within the caprock. By means of contact angle measurements, experimental evidence was obtained showing that the water-wettability of mica and quartz is altered in the presence of CO2 under pressures typical of geological storage conditions. The alteration is more pronounced in the case of mica. Both minerals are representative of shaly caprocks and are strongly water-wet in the presence of hydrocarbons. A careful analysis of the available literature data on breakthrough pressure measurements in caprock samples confirms the existence of a wettability alteration by dense CO2, both in shaly and in evaporitic caprocks. The consequences of this effect on the maximum CO2 storage pressure and on CO2 storage capacity in the underground reservoir are discussed. For hydrocarbon reservoirs that were initially close to capillary leakage, the maximum allowable CO2 storage pressure is only a fraction of the initial reservoir pressure. [source]


    Gas breakthrough experiments on fine-grained sedimentary rocks

    GEOFLUIDS (ELECTRONIC), Issue 1 2002
    A. Hildenbrand
    Abstract The capillary sealing efficiency of fine-grained sedimentary rocks has been investigated by gas breakthrough experiments on fully water saturated claystones and siltstones (Boom Clay from Belgium, Opalinus Clay from Switzerland and Tertiary mudstone from offshore Norway) of different lithological compositions. Sand contents of the samples were consistently below 12%, major clay minerals were illite and smectite. Porosities determined by mercury injection lay between 10 and 30% while specific surface areas determined by nitrogen adsorption (BET method) ranged from 20 to 48 m2 g , 1. Total organic carbon contents were below 2%. Prior to the gas breakthrough experiments the absolute (single phase) permeability (kabs) of the samples was determined by steady state flow tests with water or NaCl brine. The kabs values ranged between 3 and 550 nDarcy (3 × 10,21 and 5.5 × 10,19 m2). The maximum effective permeability to the gas-phase (keff) measured after gas breakthrough on initially water-saturated samples extended from 0.01 nDarcy (1 × 10,23 m2) up to 1100 nDarcy (1.1 × 10,18 m2). The residual differential pressures after re-imbibition of the water phase, referred to as the ,minimum capillary displacement pressures' (Pd), ranged from 0.06 to 6.7 MPa. During the re-imbibition process the effective permeability to the gas phase decreases with decreasing differential pressure. The recorded permeability/pressure data were used to derive the pore size distribution (mostly between 8 and 60 nm) and the transport porosity of the conducting pore system (10 -5,10 -2%). Correlations could be established between (i) absolute permeability coefficients and the maximum effective permeability coefficients and (ii) effective or absolute permeability coefficients and capillary sealing efficiency. No correlation was found between the capillary displacement pressures determined from gas breakthrough experiments and those derived theoretically by mercury injection. [source]


    Thermodynamic study of capillary pressure curves based on free energy minimization

    GEOFLUIDS (ELECTRONIC), Issue 3 2001
    Y. Deng
    Abstract This paper presents a new method for pore level network simulation of the distribution of two immiscible phases in a permeable medium. The method requires that the Helmholtz free energy of the system , the medium and the two phases contained within the pore space , be a minimum at all saturation states. We describe the method here and show some typical results from a computer algorithm that implements it. The results include (i) an explanation of the ,scanning' behaviour of capillary pressure curves based wholly on the free energy minimization, (ii) predictions of capillary pressure at arbitrary wetting states, including negative capillary pressures, and (iii) illustrations of how the minimized free energy changes along the scanning curves. The method also predicts the known dependency of the capillary pressure on the pore size distribution and interfacial tension. The current work is restricted to two-dimensional networks, but the free energy minimization appears to be generalizable to three dimensions and to more than two fluid phases. Moreover, functions generated through the minimization, specifically contact areas between the medium surface and the phases, appear to have applications predicting other multiphase petrophysical properties. [source]


    Pristine New Zealand forest soil is a strong methane sink

    GLOBAL CHANGE BIOLOGY, Issue 1 2004
    Sally J. Price
    Abstract Methanotrophic bacteria oxidize methane (CH4) in forest soils that cover ,30% of Earth's land surface. The first measurements for a pristine Southern Hemisphere forest are reported here. Soil CH4 oxidation rate averaged 10.5±0.6 kg CH4 ha,1 yr,1, with the greatest rates in dry warm soil (up to 17 kg CH4 ha,1 yr,1). Methanotrophic activity was concentrated beneath the organic horizon at 50,100 mm depth. Water content was the principal regulator of (r2=0.88) from the most common value of field capacity to less than half of this when the soil was driest. Multiple linear regression analysis showed that soil temperature was not very influential. However, inverse co-variability confounded the separation of soil water and temperature effects in situ. Fick's law explained the role of water content in regulating gas diffusion and substrate supply to the methanotrophs and the importance of pore size distribution and tortuosity. This analysis also showed that the chambers used in the study did not affect the oxidation rate measurements. The soil was always a net sink for atmospheric CH4 and no net CH4 (or nitrous oxide, N2O) emissions were measured over the 17-month long study. For New Zealand, national-scale extrapolation of our data suggested the potential to offset 13% of CH4 emissions from ca. 90 M ruminant animals. Our average was about 6.5 times higher than rates reported for most Northern Hemisphere forest soils. This very high was attributed to the lack of anthropogenic disturbance for at least 3000,5000 years and the low rate of atmospheric nitrogen deposition. Our truly baseline data could represent a valid preagricultural, preindustrial estimate of the soil sink for temperate latitudes. [source]


    Influence of Microsilica Content on the Slag Resistance of Castables Containing Porous Corundum,Spinel Aggregates

    INTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 6 2008
    Wen Yan
    Corrosion of five corundum,spinel castables containing the same porous aggregates and different matrices by converter slag (C/S=3) was conducted using the static crucible test through the counting pixels method, XRD, SEM, EDAX, and so on. It was found that the corrosion and penetration resistance depend on the microsilica content. Microsilica content strongly affects liquid phase formation in the matrix, changes the porosity, pore size distribution of matrix, and viscosity of slag penetrated, and thus affects its corrosion and penetration resistance. Increasing microsilica, decreasing the porosity, or increasing the viscosity of the penetrating slag improves, whereas increasing the pore size or liquid content reduces the penetration and corrosion resistance. The penetration resistance increased abruptly with an increase of the microsilica content from 0.65 to 1.95 wt%, but changed slightly with increase of the microsilica content from 1.95 to 3.90 wt%. The corrosion resistance increased with an increase of the microsilica content from 0 to 2.60 wt%, but slightly decreased with a further increase of the microsilica content to 3.90 wt%. 1.95,2.60 wt% microsilica leads to a compromise between low corrosion and low penetration. [source]


    Moisture sorption isotherms and thermodynamic properties of apple Fuji and garlic

    INTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 10 2008
    Mariana A. Moraes
    Summary The moisture equilibrium isotherms of garlic and apple were determined at 50, 60 and 70 °C using the gravimetric static method. The experimental data were analysed using GAB, BET, Henderson,Thompson and Oswin equations. The isosteric heat and the differential entropy of desorption were determined by applying Clausius,Clapeyron and Gibbs,Helmholtz equations, respectively. The GAB equation showed the best fitting to the experimental data (R2 > 99% and E% < 10%). The monolayer moisture content values for apple were higher than those for garlic at the studied temperatures; the values varied from 0.050 to 0.056 and from 0.107 to 0.168 for garlic and apple, respectively. The isosteric heat and the differential entropy of desorption were estimated in function of the moisture content. The values of these thermodynamic properties were higher for apple (in range 48,100 kJ mol,1 and 14,150 J mol,1 K,1) than for garlic (in range 43,68 kJ mol,1 and 0,66 J mol,1 K,1). The water surface area values decreased with increasing temperature. The Kelvin and the Halsey equations were used to calculate the pore size distribution. [source]


    Sub-micron spongiform porosity is the major ultra-structural alteration occurring in archaeological bone

    INTERNATIONAL JOURNAL OF OSTEOARCHAEOLOGY, Issue 6 2002
    G. Turner-Walker
    Abstract Total pore volume and pore size distribution are indicators of the degree of post-mortem modification of bone. Direct measurements of pore size distribution in archaeological bones using mercury intrusion porosimetry (HgIP) and back scattered scanning electron microscopy (BSE-SEM) reveal a common pattern in the changes seen in degraded bone as compared to modern samples. The estimates of pore size distribution from HgIP and direct measurement from the BSE-SEM images show remarkable correspondence. The coupling of these two independent approaches has allowed the diagenetic porosity changes in human archaeological bone in the >0.01 µm range to be directly imaged, and their relationship to pre-existing physiological pores to be explored. The increase in porosity in the archaeological bones is restricted to two discrete pore ranges. The smaller of these two ranges (0.007,0.1 µm) lies in the range of the collagen fibril (0.1 µm diameter) and is presumably formed by the loss of collagen, whereas the larger pore size distribution is evidence of direct microbial alteration of the bone. HgIP has great potential for the characterization of microbial and chemical alteration of bone. Copyright © 2002 John Wiley & Sons, Ltd. [source]


    Paste extrusion control and its influence on pore size properties of PTFE membranes

    ADVANCES IN POLYMER TECHNOLOGY, Issue 3 2007
    Radium Huang
    Abstract Polytetrafluoroethylene (PTFE) is a remarkable membrane material. Owing to its high-melting point, PTFE fine powder cannot be processed using conventional melting processing methods. Instead, techniques such as paste extrusion, rolling, and sintering have to be employed. Each processing step has an important influence on the final pore size quality within the membrane. In this paper, a PID controller (proportional-integral-derivative controller) was used to improve the properties of PTFE paste during the extrusion process and the quality of the PTFE membrane. A range of lubricant content (18, 20, and 22 wt%) was used to monitor the pressure drop at different extrusion speeds (0.5, 1, and 2 mm/s) and reduction ratios (RR = 26.47, 47.06, 80.06). It was found that a higher lubricant content and a higher reduction ratio resulted in a lower pressure drop. It was also found that a higher stretching temperature tends to result in larger pore size and broader pore size distribution at the same stretching rate. At a monitored and controlled constant low-extrusion speed, the porosity of PTFE membrane was increased from 38% to 55% and the mean pore size was decreased from 0.22 to 0.15 ,m because of less migration and more uniform distribution of lubricant during extrusion. Properties and the associated property uniformity of the PTFE extrudate affect the subsequent membrane-forming process and the final pore size and size distribution significantly. © 2008 Wiley Periodicals, Inc. Adv Polym Techn 26:163,172, 2007; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20099 [source]


    Microporous activated carbon spheres prepared from resole-type crosslinked phenolic beads by physical activation

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2008
    Arjun Singh
    Abstract Microporous activated carbon spheres (ACSs) with a high specific Brunauer,Emmet,Teller (BET) surface area were prepared from resole-type spherical crosslinked phenolic beads (PBs) by physical activation. The PBs used as precursors were synthesized in our laboratory through the mixing of phenol and formaldehyde in the presence of an alkaline medium by suspension polymerization. The effects of the gasification time, temperature, and flow rate of the gasifying agent on the surface properties of ACSs were investigated. ACSs with a controllable pore structure derived from carbonized PBs were prepared by CO2 gasification. Surface properties of ACSs, such as the BET surface area, pore volume, pore size distribution, and pore diameters, were characterized with BET and Dubinin,Reduchkevich equations based on N2 adsorption isotherms at 77 K. The results showed that ACSs with a 32,88% extent of burn-off with CO2 gasification exhibited a BET surface area ranging from 574 to 3101 m2/g, with the pore volume significantly increased from 0.29 to 2.08 cm3/g. The pore size and its distribution could be tailored by the selection of suitable conditions, including the gasification time, temperature, and flow rate of the gasifying agents. The experimental results of this analysis revealed that ACSs obtained under different conditions were mainly microporous. The development of the surface morphology of ACSs was also studied with scanning electron microscopy. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source]


    Effects of oxidation time on the structure and properties of polyacrylonitrile-based activated carbon hollow fiber

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007
    Junfen Sun
    Abstract Polyacrylonitrile (PAN) hollow fibers were pretreated with ammonium dibasic phosphate, then further oxidized in air, carbonized in nitrogen, and activated with carbon dioxide. The effects of oxidation time of PAN hollow fiber precursor on the microstructure, specific surface, pore size distribution, and adsorption properties of PAN-based activated carbon hollow fiber (PAN-ACHF) were studied in this work. Both of specific surface area and adsorption ratio to VB12 reach maximums when PAN hollow fibers are oxidized for 5 h in air. The adsorption ratios for creatinine are all higher than 90% over all oxidation time. After 5 h of oxidation, the number of pores on the surface obviously increases, and the pore size is uniform. After 7 h of oxidation, the number of macropores in PAN-ACHF increases. The dominant pore sizes of mesopores in PAN-ACHF range from 2 to 5 nm. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source]


    Thermal analysis of merino wool fibres without internal lipids

    JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007
    M. Martí
    Abstract Merino wool is made up of cuticle and cortical cells held together by the cell membrane complex (CMC), which contains a small amount of internal lipids (IWL) (1.5% by mass). IWL have been extracted from wool on account of their considerable dermatological interest owing to their proportion of ceramides. IWL have been extracted by different methods and solvents, methanol and acetone at laboratory and pilot plant levels. Thermal analysis of these extracted wool fibers is presented using thermogravimetry (TG) and differential scanning calorimetry (DSC). TG provides a measurement of the weight loss of the sample as a function of time and temperature. DSC gives information about possible structure modification of extracted wool fibers. Thermoporometry was applied to evaluate the pore size distribution of extracted wool fibers. The results showed that the extraction process increased the pore size distribution and the cumulated pore volume, which is consistent with some changes in the extracted wool CMC. Extracted fiber becomes more hydrophilic and absorbs a large amount of water. We can conclude that the lipid extraction of wool produced no relevant changes in the crystalline fraction when extracted with acetone. However, part of the amorphous keratin material was extracted with methanol, the rest of the crystalline material becoming more stable. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 545,551, 2007 [source]


    Activated carbon surface modifications by adsorption of bacteria and their effect on aqueous lead adsorption

    JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 12 2001
    J Rivera-Utrilla
    Abstract The adsorption of Escherichia coli on different activated carbons has been studied. The activated carbon samples used have been characterized, determining their surface area, pore size distribution, elemental analysis, mineral matter analysis and pH of the point of zero charge. The adsorption capacity of these carbons increased with their hydrophobicity and macropore volume. The number of bacteria adsorbed on the demineralized activated carbon in a solution of pH value equal to the iso-electric point of the carbon was negligible. However, in the presence of cations the proportions of bacterial cells adsorbed were 87.8% (Fe3+), 54.7% (Ca2+) and 24.8% (Mg2+) respectively. This increase in adsorption capacity in the presence of electrolytes has been explained on the basis of both the reduction in electrostatic free energy and the increase in cell surface hydrophobicity due to the metal bound by some compounds of the cell membrane. When the solution pH was intermediate between the pH values of the point of zero charge of the carbon and bacteria the number of bacteria adsorbed increased due to the attractive interactions between the carbon and bacteria. The adsorption of bacteria on activated carbons decreased the porosity and increased the negative charge density of the latter. Depending on the experimental conditions used, the presence of bacteria can enhance the capacity of activated carbons to adsorb lead. © 2001 Society of Chemical Industry [source]


    Polyamide-imide nanofiltration hollow fiber membranes with elongation-induced nano-pore evolution

    AICHE JOURNAL, Issue 6 2010
    Shi Peng Sun
    Abstract The molecular design of nanoporous membranes with desired morphology and selectivity has attracted significant interest over the past few decades. A major problem in their applications is the trade-off between sieving property and permeability. Here, we report the discovery of elongation-induced nano-pore evolution during the external stretching of a novel polyamide-imide nanofiltration hollow fiber membrane in a dry-jet wet-spinning process that simultaneously leads to a decreased pore size but increased pure water permeability. The molecular weight cutoff, pore size, and pore size distribution were finely tuned using this approach. AFM and polarized FTIR verified the nano-pore morphological evolution and an enhanced molecular orientation in the surface skin layer. The resultant nanofiltration membranes exhibit highly effective fractionation of the monovalent and divalent ions of NaCl/Na2SO4 binary salt solutions. More than 99.5% glutathione can be rejected by the nanofiltration membranes at neutral pH, offering the feasibility of recovering this tripeptide. © 2009 American Institute of Chemical Engineers AIChE J, 2010 [source]


    Theoretical studies on structural and electrical properties of PES/SPEEK blend nanofiltration membrane

    AICHE JOURNAL, Issue 8 2009
    A. F. Ismail
    Abstract Polyethersulfone (PES) nanofiltration membranes were prepared using a simple dry-jet wet spinning technique with different contents of sulfonated poly(ether ether ketone) (SPEEK) ranging from 0 to 4 wt %. The structural parameters (rp and Ak/,x) and electrostatic properties (, and X) of the blend membranes were deduced by employing the combination of irreversible thermodynamic model, steric hindrance pore (SHP) model, and Teorell-Meyer-Sievers (TMS) model. The modeling results obtained have been analyzed and discussed. The mean pore radius and pore size distribution of the blends were also determined based on the theoretical models. The results showed that pore radius increased with increasing the concentration of SPEEK from 0 to 2 wt % but decreased with a further increase in SPEEK content. The water flux, however, showed a systematically increase with increasing SPEEK content. The SPEEK also showed significant effect on membrane electrical properties. Both effective charge density and ratio of effective charge density to electrolyte solution increased with increasing concentration of SPEEK in the dope solution, reaching a value of ,21.02 and ,2.29, respectively. The pore radius which was determined by using different transport models has also been analyzed and discussed. It is found that the addition of SPEEK into dope solution is one of the paramount parameters in developing the negatively charged nanofiltration membrane with enhanced water flux while retaining the pore radius in the nanometer range. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source]


    Exploration of ionic modification in dual-layer hollow fiber membranes for long-term high-performance protein separation

    AICHE JOURNAL, Issue 2 2009
    Yi Li
    Abstract Two types of ionic modification approaches (i.e., sulfonation and triethylamination) were applied with the aid of dual-layer hollow fiber technology in this work to fine tune the pore size and pore size distribution, introduce the electrostatic interaction, and reduce membrane fouling for long-term high-performance protein separation. A binary protein mixture comprising bovine serum albumin (BSA) and hemoglobin (Hb) was separated in this work. The sulfonated fiber exhibits an improved BSA/Hb separation factor at pH = 6.8 compared with as-spun fibers but at the expense of BSA sieving coefficient. On the other hand, the triethylaminated fiber reveals the best and most durable separation performance at pH = 4.8. Its BSA/Hb separation factor is maintained above 80 for 4 days and maximum BSA sieving coefficient reaches 33%. Therefore, this study documents that an intelligent combination of both size-exclusion and electrostatic interaction can synergistically enhance protein separation performance in both purity and concentration. © 2008 American Institute of Chemical Engineers AIChE J, 2009 [source]


    Quantitative characterization of sphere-templated porous biomaterials

    AICHE JOURNAL, Issue 4 2005
    A. J. Marshall
    Abstract Three-dimensional (3-D) porous hydrogels were fabricated by polymerizing 2-hydroxyethyl methacrylate around templates of random close-packed poly(methyl methacrylate) microspheres with nominal diameter of 5 or 15 ,m. The templates were leached out to create networks of interconnected spherical pores. Applications for sphere-templated porous biomaterials include scaffolds for tissue engineering and spatial control of wound healing. This study describes an approach to characterizing pore structure and predicting permeability of sphere-templated porous hydrogels. The materials were embedded in resin, and 1-,m-plane sections were digitally analyzed with fluorescence microscopy. The porosity and pore size distribution were determined from stereological interpretation, and we present novel techniques for obtaining the pore throat size distribution, the number of pore throats per pore, and the tortuosity. A simple apparatus is also introduced for measurement of the hydraulic permeability. Permeability predictions based on quantitative microscopy measurements and on stereology were found to agree closely with permeability measurements. The aptness of the Kozeny equation for spherically pored materials is also investigated. © 2005 American Institute of Chemical Engineers AIChE J, 2005 [source]


    Pore-size effects on activated-carbon capacities for volatile organic compound adsorption

    AICHE JOURNAL, Issue 8 2002
    Mei-Chiung Huang
    Gas-phase adsorption of acetone and n-hexane by activated carbons with different pore structures was investigated. The carbons were prepared from a bituminous coal with KOH activation. Increasing the activation temperature increased both the porosity and pore size. The equilibrium adsorption capacity for the organic compounds increased with the carbon porosity, but not proportionally. The percentage of pore volume utilized showed a decreasing trend with the porosity development for acetone adsorption, while an increasing trend was observed for n-hexane. By incorporating pore size distribution with the Dubinin-Radushkevich equation using an inverse proportionality between the micropore size and adsorption energy, the isotherms for adsorption onto different carbons can be well predicted. Simulations indicated that the adsorption energy, which is an inverse function of the micropore size, determines the adsorption capacity. Different effects of porosity development were observed for different adsorbates. [source]


    Monolithic poly(glycidyl methacrylate- co -divinylbenzene) capillary columns functionalized to strong anion exchangers for nucleotide and oligonucleotide separation

    JOURNAL OF SEPARATION SCIENCE, JSS, Issue 16 2006
    Wolfgang Wieder
    Abstract In the present work, poly(glycidyl methacrylate- co -divinylbenzene) monoliths were synthesized and further derivatized to obtain strong anion exchange supports. Capillary monoliths (65×0.2 mm id) were prepared in situ by copolymerization of glycidyl methacrylate and divinylbenzene, employing 1-decanol and tetrahydrofuran as porogens. The free epoxy groups were derivatized in a two step synthesis to obtain quaternary ammonium functionalities. On testing the pressure stability of the synthesized monolith, a highly linear dependence between flow rate and pressure drop was obtained, indicating the high stability of the material even at high flow rates. The morphology of the copolymer was investigated by scanning electron microscopy. Mercury intrusion porosimetry showed a narrow pore size distribution, having a maximum at 439 nm. On recording a van Deemter plot the number of theoretical plates per meter was found to be 59 324. The produced strong anion exchange monoliths turned out to be highly suitable for the separation of nucleotides and oligonucleotides. [source]


    Microstructure,Property Correlations in Industrial Thermal Barrier Coatings

    JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 7 2004
    Anand A. Kulkarni
    This paper describes the results from multidisciplinary characterization/scattering techniques used for the quantitative characterization of industrial thermal barrier coating (TBC) systems used in advanced gas turbines. While past requirements for TBCs primarily addressed the function of insulation/life extension of the metallic components, new demands necessitate a requirement for spallation resistance/strain tolerance, i.e., prime reliance, on the part of the TBC. In an extensive effort to incorporate these TBCs, a design-of-experiment approach was undertaken to develop tailored coating properties by processing under varied conditions. Efforts focusing on achieving durable/high-performance coatings led to dense vertically cracked (DVC) TBCs, exhibiting quasi-columnar microstructures approximating electron-beam physical-vapor-deposited (EB-PVD) coatings. Quantitative representation of the microstructural features in these vastly different coatings is obtained, in terms of porosity, opening dimensions, orientation, morphologies, and pore size distribution, by means of small-angle neutron scattering (SANS) and ultra-small-angle X-ray scattering (USAXS) studies. Such comprehensive characterization, coupled with elastic modulus and thermal conductivity measurements of the coatings, help establish relationships between microstructure and properties in a systematic manner. [source]


    Transparent Polycrystalline Alumina Ceramic with Sub-Micrometre Microstructure by Means of Electrophoretic Deposition

    MATERIALWISSENSCHAFT UND WERKSTOFFTECHNIK, Issue 4 2006
    A. Braun
    Abstract The optical quality attainable in coarse-grained polycrystalline alumina is severely limited by grain-boundary scattering, which is inherent to non-cubic materials. The optical properties of sub-micrometre polycrystalline alumina are of growing interest triggered by the fact that a decrease in the grain sizes of the final sintered material yields an improvement in the optical quality while the scattering mechanism changes as the grain size becomes comparable with the wavelength of light. To achieve transparent alumina ceramics with a fine-grained microstructure, however, porosity and other defects must be avoided. This necessitates the optimization of processing and sintering procedures. Electrophoretic deposition (EPD) is a colloidal process in which ceramic bodies are directly shaped from a stable suspension by application of an electric field. Electrophoretic deposition enables the formation of homogeneous, uniform green microstructures with high density, which can be sintered to transparency. It is a simple and precise technique to synthesize not only monoliths, but also composites with complex geometries [1]. Alumina green bodies were deposited from stabilized aqueous suspensions with and without doping. Green alumina compacts were evaluated based on their pore size distribution and density. Densification behaviour was characterized by dilatometric studies conducted at constant heating rate. Samples were sintered at different temperatures with subsequent post-densification by hot isostatic pressing. Transparency was evaluated by means of spectroscopic measurements. The measured in-line transmission of the samples at 645 nm was more than 50,% and that is 58,% of the value of sapphire. The influence of dopings on transparency was investigated. The mechanical properties of the samples were tested. [source]


    Melt processed microporous films from compatibilized immiscible blends with potential as membranes

    POLYMER ENGINEERING & SCIENCE, Issue 4 2002
    M. Xanthos
    Microporous flat films with potential as membranes were produced via melt processing and post-extrusion drawing from immiscible polypropylene/polystyrene blends containing a compatibilizing copolymer. The blends were first compounded in a co-rotating twin-screw extruder and subsequently extruded through a sheet die to obtain the precursor films. These were uniaxially drawn (100%,500%) with respect to the original dimensions to induce porosity and then post-treated at elevated temperatures to stabilize the resultant structure, which consisted of uniform microcracks in the order of a few nanometers in width. The effects of blend composition and extrusion process parameters on surface and cross-sectional porosity and solvent permeability of the prepared films are presented and related to specific microstructural features of the films before and after drawing. Finite element modeling of the stretching operation in the solid state yielded a successful interpretation of the blend response to uniaxial tension that resulted in microcrack formation. Comparison of some of the novel microporous structures of this work with commercial membranes prepared by solvent-based phase inversion processes suggests comparable pore size and porosity ranges, with narrower pore size distribution. [source]


    Synthesis of Microporous Carbon Foams as Catalyst Supports

    CHEMICAL ENGINEERING & TECHNOLOGY (CET), Issue 4 2010
    F. Glenk
    Abstract Microporous carbon foams were synthesized as structured catalyst supports by the carbide-derived carbon (CDC) method. The self-supporting foams showed a narrow pore size distribution which seems to induce shape-selective effects during reactions. The applicability of these materials as supports for active metals was tested in a hydrogenation reaction of different olefins with a CDC powder wet impregnated with platinum. [source]


    Self-Assembling of Er2O3,TiO2 Mixed Oxide Nanoplatelets by a Template-Free Solvothermal Route

    CHEMISTRY - A EUROPEAN JOURNAL, Issue 45 2009
    Beatriz Julián-López Dr.
    Abstract An easy solvothermal route has been developed to synthesize the first mesoporous Er2O3,TiO2 mixed oxide spherical particles composed of crystalline nanoplatelets, with high surface area and narrow pore size distribution. This synthetic strategy allows the preparation of materials at low temperature with interesting textural properties without the use of surfactants, as well as the control of particle size and shape. TEM and Raman analysis confirm the formation of nanocrystalline Er2O3,TiO2 mixed oxide. Mesoscopic ordered porosity is reached through the thermal decomposition of organic moieties during the synthetic process, thus leading to a template-free methodology that can be extended to other nanostructured materials. High specific surface areas (up to 313,m2,g,1) and narrow pore size distributions are achieved in comparison to the micrometric material synthesized by the traditional sol,gel route. This study opens new perspectives in the development, by solvothermal methodologies, of multifunctional materials for advanced applications by improving the classical pyrochlore properties (magnetization, heat capacity, catalysis, conductivity, etc.). In particular, since catalytic reactions take place on the surface of catalysts, the high surface area of these materials makes them promising candidates for catalysts. Furthermore, their spherical morphology makes them appropriate for advanced technologies in, for instance, ceramic inkjet printers. [source]


    High Surface Area, Mesoporous, Glassy Alumina with a Controllable Pore Size by Nanocasting from Carbon Aerogels

    CHEMISTRY - A EUROPEAN JOURNAL, Issue 5 2005
    Wen-Cui Li Dr.
    Abstract A strategy to synthesize amorphous, mesoporous alumina by nanocasting has been developed, involving carbon aerogel as a hard template and aluminum nitrate solution as an alumina precursor. The alumina generated exhibits small, transparent granules with a 3,6 mm diameter and has inherited the three-dimensional network structure of the carbon template. The mesopore surface area of the alumina can be as high as 365 m2,g,1, and the pore volume reaches 1.55 cm3,g,1 after calcination at 600,°C in air for 8 h. The pore parameters can be varied within a certain range by variation of the carbon aerogel template and the loading amount of the alumina precursor. At high loadings, the obtained glassy alumina clearly has a bimodal pore size distribution in the mesopore range. [source]