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Monoliths
Kinds of Monoliths Selected AbstractsPRESELI DOLERITE BLUESTONES: AXE-HEADS, STONEHENGE MONOLITHS, AND OUTCROP SOURCESOXFORD JOURNAL OF ARCHAEOLOGY, Issue 1 2006OLWEN WILLIAMS-THORPE Summary. Chemical compositions and magnetic susceptibility data were compared for 12 dolerite bluestone implements including axes, axe-hammers and battle-axes, 11 Stonehenge monoliths (chemical data only), and potential source outcrops in Preseli, South Wales. Most of the studied artefacts are of spotted dolerite, a small number being unspotted dolerite. Bivariate graphs, discriminant analysis and t-tests were used singly and in combination to show, respectively, that the implements found at sites in England are mainly similar to Stonehenge monoliths, while the implements found in Wales have a variety of compositions and are much less similar to Stonehenge monoliths. The dichotomy between English and Welsh dolerite bluestone implements could be explained by exploitation of different Preseli outcrops or erratic assemblages derived from them. A small number of spotted dolerite implements have previously been shown to have chemical compositions atypical of and marginal to Preseli, suggesting the possibility of a source of spotted dolerite outside Preseli. Previously published analytical data in combination with the new implement/outcrop comparisons presented in this paper support derivation of the majority of analysed Stonehenge monoliths at one particular outcrop within the group of four identified by Thorpe et al. 15 years ago. Analysis of all the extant bluestone monoliths at Stonehenge (now possible using non-destructive methods) would allow progress in identifying monolith outcrop sources, and in understanding the links with the bluestone axe trade. [source] Selectivity, Hydrodynamics and Solvent Effects in a Monolith Cocurrent Downflow Contactor (CDC) ReactorTHE CANADIAN JOURNAL OF CHEMICAL ENGINEERING, Issue 3-4 2003Mike Winterbottoma Abstract The liquid phase hydrogenation of 2-butyne-1,4-diol (B) to cis-2-butene-1,4,-diol (C) was studied in a Monolith (CDC) Reactor. The effect of temperature, pressure, different solvents and gas and liquid feed rates on reaction rate and selectivity was determined. RTD measurements were made under different hydrodynamic conditions. The liquid flow was largely laminar with evidence of a stagnant wall film. Selectivity to C was observed to increase with hydrogen pressure and approaches 1 at high superficial gas velocities and conversion of B (>95%) as plug flow is approached. The flow regime was of influence on selectivity and kinetics, which was described by a dual site Langmuir-Hinshelwood mechanism. L'hydrogénation en phase liquide du butyne-2-diol-1,4 B en cis-butène-2-diol-1,4 C a été étudiée dans un réacteur à monolithe (CDC). On a déterminé l'effet de la température, de la pression, des différents solvants et des vitesses d'alimentation de gaz et de liquide sur la vitesse de réaction et la sélectivité. Des mesures de distribution de temps de séjour ont été effectuées pour différentes conditions hydrodynamiques. L'écoulement du liquide est largement laminaire avec un film de paroi stagnant évident. On a observé que la sélectivité pour C augmentait avec la pression de l'hydrogène et s'approchait de 1 à des vitesses de gaz superficielles élevées et à conversion de B élevée (>95%) quand l'écoulement piston devient piston. Le régime d'écoulement a une influence sur la sélectivité et la cinétique, et celle-ci est bien décrite par un mécanisme à site double de Langmuir-Hinshelwood. [source] Ring-Opening Polymerization with Synergistic Co-monomers: Access to a Boronate-Functionalized Polymeric Monolith for the Specific Capture of cis -Diol-Containing Biomolecules under Neutral Conditions,ANGEWANDTE CHEMIE, Issue 36 2009Lianbing Ren Molekulare Teamarbeit: Synergistische Comonomere in einem Boronat-funktionalisierten Polymermonolithen wirken wie ein einzelner Boronsäureligand vom Wulff-Typ und ermöglichen die spezifische Bindung von cis -Diol-Biomolekülen unter neutralen Bedingungen (siehe Schema). Beim Ansäuern des Mediums wird die Aminogruppe protoniert und die B-N-Koordination aufgehoben, was zur Freisetzung des cis -Diols vom Monolithen führt. [source] Hard Macrocellular Silica Si(HIPE) Foams Templating Micro/Macroporous Carbonaceous Monoliths: Applications as Lithium Ion Battery Negative Electrodes and Electrochemical CapacitorsADVANCED FUNCTIONAL MATERIALS, Issue 19 2009Nicolas Brun Abstract By using Si(HIPEs) as hard, exotemplating matrices, interconnected macro-/microporous carbon monolith-type materials with a surface area of around 600,m2 g,1 are synthesized and shaped. The carbonaceous foams exhibit a conductivity of 20,S cm,1, addressed with excellent mechanical properties (Young's modulus of 0.2,GPa and toughness of 13,J g,1, when the carbon core is optimized). The above-mentioned specificities, combined with the fact that the external shape and size can be easily designed on demand, are of primary importance for applications. The functionality of these carbonaceous monoliths is tested as both an electrochemical capacitor and a lithium ion negative electrode. The electrochemical capacitors' voltage,current profiles exhibit a non-ideal rectangular response, confirming the double-layer behavior of the carbon studied, while the charge-discharge current profile of the electric double-layer capacitor is directly proportional to the scan where the current response during charge and discharge exhibits high reversibility. When acting as a lithium ion negative electrode, after initial irreversibility, a good cyclability is obtained, associated with a stable capacity of 200,mA h g,1 during the first 50 cycles at a reasonable current density (C/10). [source] Synthesis of ZSM-5 Films and Monoliths with Bimodal Micro/Mesoscopic StructuresADVANCED FUNCTIONAL MATERIALS, Issue 1 2004I. Cho Abstract A route to synthesize ZSM-5 crystals with a bimodal micro/mesoscopic pore system has been developed in this study; the successful incorporation of the mesopores within the ZSM-5 structure was performed using tetrapropylammonium hydroxide (TPAOH)-impregnated mesoporous materials containing carbon nanotubes in the pores, which were encapsulated in the ZSM-5 crystals during a solid rearrangement process within the framework. Such mesoporous ZSM-5 zeolites can be readily obtained as powders, thin films, or monoliths. [source] SiOC Ceramic Monoliths with Hierarchical PorosityINTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 4 2010Cekdar Vakifahmetoglu SiOC glass monoliths possessing hierarchical porosity were produced by a one-pot processing method. Periodic mesoporous organosilica (PMO) particles were embedded into a foamed siloxane preceramic polymer. After pyrolysis at 1000°C in inert atmosphere, open celled, permeable SiOC ceramic monoliths with a high amount of pores, ranging in size from hundred of micrometers to a few nanometers, were obtained. The components possessed a specific surface area of 137 m2/g, indicating the retention of most of the mesopores after the pyrolytic conversion of the PMO precursor particles. These fillers converted to truncated rhombic dodecahedral SiOC mesoporous micron-sized grains, homogeneously distributed throughout the SiOC cellular matrix. The produced porous ceramics possessed compression strength of about 1.7 MPa, which is adequate for their use in several engineering applications. [source] A Room Temperature Ionic Liquid (RTIL)-Mediated, Non-Hydrolytic Sol,Gel Methodology to Prepare Molecularly Imprinted, Silica-Based Hybrid Monoliths for Chiral Separation,ADVANCED MATERIALS, Issue 24 2006H.-F. Wang Silica-based hybrid molecularly imprinted polymer (MIP) monoliths with good chiral recognition ability are synthesized (see figure) using a novel method, a room temperature ionic liquid (RTIL)-mediated, non-hydrolytic sol,gel technique. The approach avoids the cracking and shrinking of the bed during drying, which is commonly associated with conventional sol,gel processing, overcomes the shortcomings associated with conventional organic-polymer-based MIP matrices, and offers improved selectivity. [source] Carbon Nanofibers Uniformly Grown on ,-Alumina Washcoated Cordierite Monoliths,ADVANCED MATERIALS, Issue 12 2006E. García-Bordejé A uniform layer of carbon nanofibers is grown on a cordierite monolith by first coating the monolith with a thin layer of ,-alumina. The nanofibers form a thick, uniform layer on the monolith walls as shown in the figure, leading to the formation of a mesoporous and mechanically robust composite. The absence of microporosity in the composite and the ability to tune the thickness of the nanofiber layer suggests that these nanofibers/monolith composites may be useful as catalyst supports for liquid-phase catalytic reactions. [source] Solid phase peptide synthesis on epoxy-bearing methacrylate monolithsJOURNAL OF PEPTIDE SCIENCE, Issue 12 2004E. Vlakh Abstract Monoliths based on a copolymer of glycidyl methacrylate (GMA) and ethylene dimethacrylate (EDMA) can be used directly as sorbents for affinity chromatography after solid phase peptide synthesis. The quality of the synthesized products, the amount of grown peptides on a support and the reproducibility of the process must be considered. A determination of the quantity of the introducing ,-Ala (and, consequently, the total amount of synthesized peptide) was carried out. Three peptides complementary to recombinant tissue plasminogen activator (t-PA) have been synthesized using Fmoc-chemistry on GMA-EDMA disks. The peptidyl ligands were analysed by amino acid analysis, ES-MS and HPLC methods. The affinity binding parameters were obtained from frontal elution data. The results were compared with those established for GMA-EDMA affinity sorbents formed by the immobilization of the same but separately synthesized and purified ligands. The immobilization on GMA-EDMA disks was realized using a one-step reaction between the amino groups of the synthetic ligand and the original epoxy groups of monolithic material. The affinity constants found for two kinds of sorbent did not vary significantly. Finally, the directly obtained affinity sorbents were tested for t-PA separation from a cellular supernatant. Copyright © 2004 European Peptide Society and John Wiley & Sons, Ltd. [source] Copper-mediated radical polymerization on a microcellular monolith surfaceJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 5 2004Laurence Moine Abstract High-capacity microcellular monoliths were prepared by a two-step process, including the synthesis of a bromoester-functionalized scaffold by the copolymerization of a highly concentrated emulsion and an in situ surface polymerization of methyl methacrylate with atom transfer radical polymerization. The influence of various parameters, such as the feed ratio, the concentration of immobilized bromoester groups, and the presence of a spacer group on the poly(methyl methacrylate) loading, was studied. Monoliths with capacities of up to 7 mmol g,1 were obtained. Thermogravimetric analyses, scanning electron microscopy experiments, and mercury intrusion porosimetry measurements were used for the characterization of the final materials. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1216,1226, 2004 [source] Visible light initiated polymerization of styrenic monolithic stationary phases using 470,nm light emitting diode arraysJOURNAL OF SEPARATION SCIENCE, JSS, Issue 1 2010Zarah Walsh Abstract Poly(styrene- co -divinylbenzene) monolithic stationary phases have been synthesized for the first time by photoinitiated polymerization. An initiator composed of (+)-(S)-camphorquinone/ethyl-4-dimethylaminobenzoate/N- methoxy-4-phenylpyridinium tetrafluoroborate was activated using a 470,nm light emitting diode array as the light source. Spatially controlled polymerization of styrenic monoliths has been achieved within specific sections of a 100,,m id polytetrafluoroethylene-coated fused-silica capillary using simple photo masking. The sharpness of the edges was confirmed by optical microscopy, while SEM was used to verify a typical porous, globular morphology. Flow resistance data were used to assess the permeability of the monoliths and they were found to have good flow through properties with a flow resistance of 0.725,MPa/cm at 1,,L/min (water, 20°C). Conductivity profiling along the length of the capillary was used to assess their lateral homogeneity. Monoliths which were axially rotated during polymerization were found to be homogeneous along the whole length of the capillary. The monolithic stationary phases were applied to the RP gradient separation of a mixture of proteins. Column fabrication showed excellent reproducibility with the retention factor (k) having a RSD value of 2.6% for the batch and less than 1.73% on individual columns. [source] Effect of Surface Modification on the Synthesis of Pore-Filling Polymeric Monoliths in Microfiltration Membranes Made from Poly(propylene) and Poly(ethylene terephthalate)MACROMOLECULAR MATERIALS & ENGINEERING, Issue 3 2007Abdus Salam Abstract The effect of pre-modification on the interaction of macroporous substrates (membranes) with mainly micro- and mesoporous polymer monoliths has been studied. Bulk, porous polymer monoliths were synthesized to optimize the synthesis conditions and their pore morphology, and the data were used as benchmark for this study. Pre-modification of the entire pore surface of PP microfiltration membranes and PET track-etched membranes by UV-initiated grafting with PEGMA was performed using well-established methods, including coating with the photo-initiator, benzophenone. Subsequently, these membranes were functionalized by filling the pores with porous polymer monoliths from MAA and EDMA and compared with membranes that had been functionalized without the pre-modification step. The materials were characterized mainly by the degree of grafting, SEM and by the gas-adsorption-isotherm method. The DG values, after composite-membrane preparation under identical conditions, were not influenced by the pre-modification. However, it could be clearly seen from the SEM images that the pre-modification step prevents the formation of voids at the monolith-membrane pore interface. Larger specific surface area and pore volume values for composite membranes, prepared after pre-modification, fully support the SEM results. Especially large differences in pore structure between the two different composite membranes were found in the mesopore range. The results of this study indicate that it is possible to prepare porous, composite membranes where the trans-membrane transport is exclusively controlled by the pore and surface structure of a functional polymeric monolith, for example, made from a molecularly-imprinted polymer. [source] Rigid Crosslinked Polyacrylamide Monoliths with Well-Defined Macropores Synthesized by Living PolymerizationMACROMOLECULAR RAPID COMMUNICATIONS, Issue 12 2009Joji Hasegawa Abstract Rigid crosslinked polyacrylamide monoliths with well-defined macropores have been successfully fabricated by organotellurium-mediated living radical polymerization (TERP) accompanied by spinodal decomposition. The TERP forms homogeneous networks derived from N,N -methylenebis(acrylamide) (BIS), in which spinodal decomposition is induced to form macropores. Macropore diameter can be controlled from submicrons to a few microns, and also the obtained networks contain mesopores in the macroporous skeletons, which are collapsed by evaporative drying. They are promising materials with hydrophilic polyacrylamide surfaces and have enough strength to preserve the macropores from the surface tension arising in the repetitive swelling and drying that may occur in many applications. [source] Post-Synthesis Functionalization of (Meth)acrylate Based Monoliths via Electron Beam Triggered Graft PolymerizationMACROMOLECULAR RAPID COMMUNICATIONS, Issue 11 2008Matthias J. Beier Abstract Porous polymeric monoliths were prepared via electron beam triggered free radical polymerization of (meth)acrylates. Post-synthesis functionalization of these supports was accomplished via electron beam initiated free radical graft polymerization of methacryloyl-substituted NHC precursors. The grafted precursors were converted into the corresponding copper complexes. Cu-loadings were between 1.3 mg,·,g,1 and 1.5 mg,·,g,1. These supported catalysts were used in selected CO hydrosilylation and cyanosilylation reactions using a continuous flow setup. [source] Integrated microdevice for preconcentration and separation of a wide variety of compounds by electrochromatographyELECTROPHORESIS, Issue 3 2009Gaelle Proczek Abstract An integrated microdevice was developed to couple on-chip SPE to separation by channel electrochromatography. An acrylate-based monolith was synthesized within a glass microdevice by photoinitiated polymerization. It was used for both separation and preconcentration by direct injection on the head of the stationary phase or by confining the preconcentration step in a given zone of the stationary phase. The composition of the polymerization mixture was chosen to achieve a monolithic material containing both hydrophobic and charged moieties to ensure an electroosmotic flow for separation. As a consequence the extraction procedure occurs via hydrophobic and ionic interactions. Neutral, ionizable and charged compounds were successfully preconcentrated and separated within the microdevice through electrochromatographic mechanisms, highlighting the versatility of this device. The performance of the integrated microdevice was demonstrated with the preconcentration and separation of a mixture of PAHs for which a signal enhancement factor (SEF) of 270 was achieved within 120,s of preconcentration. In the case of charged and ionizable compounds, according to the electrolyte composition, contributions of both reverse-phase and ion-exchange mechanisms were used to perform effective electrochromatographic preconcentration. A SEF of 250 was obtained for the model-charged compound within 20,s of preconcentration. Finally, the potentials of on-chip preconcentrate and separate both neutral and ionized compounds have been demonstrated using a mixture of model compounds. [source] Macrocyclic polyamine-modified poly(glycidyl methacrylate- co -ethylene dimethacrylate) monolith for capillary electrochromatographyELECTROPHORESIS, Issue 11 2008Yun Tian Abstract 1,4,10,13,16-Pentaazatricycloheneicosane-9,17-dione (macrocyclic polyamine)-modified polymer-based monolithic column for CEC was prepared by ring opening reaction of epoxide groups from poly(glycidyl methacrylate- co -ethylene dimethacrylate) (GMA- co -EDMA) monolith with macrocyclic polyamine. Conditions such as reaction time and concentration of macrocyclic polyamine for the modification reaction were optimized to generate substantial EOF and enough chromatographic interactions. Anodic EOF was observed in the pH range of 2.0,8.0 studied due to the protonation of macrcyclic polyamine at the surface of the monolith. Morphology of the monolithic column was examined by SEM and the incorporation of macrocyclic polyamine to the poly(GMA- co -EDMA) monolith was characterized by infrared (IR) spectra. Successful separation of inorganic anions, isomeric benzenediols, and benzoic acid derivatives on the monolithic column was achieved for CEC. In addition to hydrophobic interaction, hydrogen bonding and electrostatic interaction played a significant role in the separation process. [source] Molecularly imprinted polymers as a tool for separation in CECELECTROPHORESIS, Issue 1-2 2007Zhao-Sheng Liu Dr. Abstract Molecularly imprinted polymers (MIPs) are synthesized in the presence of a template which results in the formation of specific recognition cavities complementary to the template in shape and chemical functionality. One of the most successful application areas of MIPs is chromatographic sorbents, which are tailor-made synthetic polymers for a given analyte. However, low efficiency of MIP columns is often observed because of slow kinetics of the template. CEC-based MIPs are thought to improve efficiency of MIP-based separation due to the enhanced flow dynamics of CEC. Another attractive feature is the miniaturized format of CEC, so that fewer templates or monomers for the molecular imprinting are consumed, a characteristic desired for ,green chemistry'. The small dimensions of a capillary demand the development of novel polymer formats that can be applied to a miniaturized system. This review discusses the various formats, i.e., the micro- or nanoparticle, the coating and the monolith, for application in CEC as well as the use in MIP syntheses and characteristics. [source] High-efficiency peptide analysis on monolithic multimode capillary columns: Pressure-assisted capillary electrochromatography/capillary electrophoresis coupled to UV and electrospray ionization-mass spectrometryELECTROPHORESIS, Issue 21 2003Alexander R. Ivanov Abstract High-efficiency peptide analysis using multimode pressure-assisted capillary electrochromatography/capillary electrophoresis (pCEC/pCE) monolithic polymeric columns and the separation of model peptide mixtures and protein digests by isocratic and gradient elution under an applied electric field with UV and electrospray ionization-mass spectrometry (ESI-MS) detection is demonstrated. Capillary multipurpose columns were prepared in silanized fused-silica capillaries of 50, 75, and 100 ,m inner diameters by thermally induced in situ copolymerization of methacrylic monomers in the presence of n -propanol and formamide as porogens and azobisisobutyronitrile as initiator. N -Ethylbutylamine was used to modify the chromatographic surface of the monolith from neutral to cationic. Monolithic columns were termed as multipurpose or multimode columns because they showed mixed modes of separation mechanisms under different conditions. Anion-exchange separation ability in the liquid chromatography (LC) mode can be determined by the cationic chromatographic surface of the monolith. At acidic pH and high voltage across the column, the monolithic stationary phase provided conditions for predominantly capillary electrophoretic migration of peptides. At basic pH and electric field across the column, enhanced chromatographic retention of peptides on monolithic capillary column made CEC mechanisms of migration responsible for separation. The role of pressure, ionic strength, pH, and organic content of the mobile phase on chromatographic performance was investigated. High efficiencies (exceeding 300,000 plates/m) of the monolithic columns for peptide separations are shown using volatile and nonvolatile, acidic and basic buffers. Good reproducibility and robustness of isocratic and gradient elution pressure-assisted CEC/CE separations were achieved for both UV and ESI-MS detection. Manipulation of the electric field and gradient conditions allowed high-throughput analysis of complex peptide mixtures. A simple design of sheathless electrospray emitter provided effective and robust low dead volume interfacing of monolithic multimode columns with ESI-MS. Gradient elution pressure-assisted mixed-mode separation CE/CEC-ESI-MS mass fingerprinting and data-dependent pCE/pCEC-ESI-MS/MS analysis of a bovine serum albumin (BSA) tryptic digest in less than 5 min yielding high sequence coverage (73%) demonstrated the potential of the method. [source] Noble metal-based catalysts for total oxidation of chlorinated hydrocarbonsENVIRONMENTAL PROGRESS & SUSTAINABLE ENERGY, Issue 3 2001José M. Toledo Catalytic total oxidation of selected chlorinated hydrocarbons utilizing several noble metal (Pt, Pd, Ru)-based catalysts was studied. Chlorinated hydrocarbons used were trichloroethylene, dichloromethane, and chlorobenzene, alone or mixed with other hydrocarbons, such as toluene. Catalysts tested were both commercially available, manufactured by Degussa AG, Süd-Chemie AG, Kataleuna GmbH, Chimet, Johnson Matthey, Prototech Co., etc., and new ones developed by Universities of Leiden in The Netherlands, Budapest in Hungary, and Wroclaw in Poland. Both forms of catalyst, sphere (particulate) and monolith, were used. Selection of the best catalyst(s) was made based on its activity, selectivity, and life. Apparent energies of activation for the reactions on these catalysts, using an empirical firstorder reaction rate, are also given. [source] Hydrogen Production via Autothermal Reforming of Diesel FuelFUEL CELLS, Issue 3 2004J. Pasel Abstract Hydrogen, for the operation of a polymer electrolyte fuel cell, can be produced by means of autothermal reforming of liquid hydrocarbons. Experiments, especially with ATR 4, which produces a molar hydrogen stream equivalent to an electrical power in the fuel cell of 3,kW, showed that the process should be preferably run in the temperature range between 700,° and 850,°. This ensures complete hydrocarbon conversion and avoids the formation of considerable amounts of methane and organic compounds in the product water. Experiments with commercial diesel showed promising results but insufficient long-term stability. Experiments concerning the ignition of the catalytic reaction inside the reformer proved that within 60,s after the addition of water and hydrocarbons the reformer reached 95% of its maximum molar hydrogen flow. Measurements, with respect to reformer start-up, showed that it takes approximately 7,min. to heat up the monolith to a temperature of 340,° using an external heating device. Modelling is performed, aimed at the modification of the mixing chamber of ATR Type 5, which will help to amend the homogeneous blending of diesel fuel with air and water in the mixing chamber. [source] Kinetics of liquid phase synthesis of ethyl tert -butyl ether from tert -butyl alcohol and ethanol catalyzed by ,-zeolite supported on monolithINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 5 2002S. Assabumrungrat This paper compared the performance of ,-zeolite and Amberlyst-15 catalysts on a liquid phase synthesis of ethyl tert -butyl ether (ETBE) from ethanol (EtOH) and tert -butyl alcohol (TBA) ,-Zeolite was synthesized and deposited on monolith support. Its structure was confirmed by an XRD measurement and its composition was analyzed by an XRF measurement. It was found that even though the catalytic activity of ,-zeolite was lower than that of Amberlyst-15, the selectivity of ETBE was much higher than that of Amberlyst-15, resulting in almost the same level of ETBE yield. The dehydration of TBA to isobutene (IB) was the major side reaction. The kinetic study of the reaction catalyzed by ,-zeolite supported on monolith was carried out by using a semibatch reactor. The effect of external mass transfer was investigated by varying stirring speeds. The activity-based rate expressions were developed taking into account of water inhibition. Three temperature levels of 323, 333, and 343 K were performed in the study to obtain the parameters in the Arrhenius's equation and the Van't Hoff's equation. © 2002 Wiley Periodicals, Inc. Int J Chem Kinet 34: 292,299, 2002 [source] Carbon Nanofibers Uniformly Grown on ,-Alumina Washcoated Cordierite Monoliths,ADVANCED MATERIALS, Issue 12 2006E. García-Bordejé A uniform layer of carbon nanofibers is grown on a cordierite monolith by first coating the monolith with a thin layer of ,-alumina. The nanofibers form a thick, uniform layer on the monolith walls as shown in the figure, leading to the formation of a mesoporous and mechanically robust composite. The absence of microporosity in the composite and the ability to tune the thickness of the nanofiber layer suggests that these nanofibers/monolith composites may be useful as catalyst supports for liquid-phase catalytic reactions. [source] Comparison of performance of heat regenerators: Relation between heat transfer efficiency and pressure dropINTERNATIONAL JOURNAL OF ENERGY RESEARCH, Issue 4 2001Françoise Duprat Abstract Heat regenerators transfer heat from one gas to another, with an intermediate storage in solids. The heat transfer surface for gas flow application should provide at the same time high surface area and low friction factor. Three geometries of heat transfer surface, monolith, stack of woven screens and bed of spheres, have been compared. Their performance was evaluated from the pressure drop of the heat regenerator working at a given heat transfer efficiency. The comparison was performed using numerical simulation and published measurements of heat transfer and flow friction characteristics. By adjusting the length and the period of the exchanger, it is possible to obtain the same heat transfer efficiency with the three geometries. Beds of spheres give very short and compact heat regenerators, working at high pressure drop. At the opposite, monoliths form long regenerators working at low pressure drop. Stacks of woven screens cover a wide range of performance: low porosity woven screens give high heat transfer efficiency and high pressure drop, while high porosity woven screens offer performance similar to that of the monoliths. Copyright © 2001 John Wiley & Sons, Ltd. [source] Bioreactors Based on Monolith-Supported Ionic Liquid Phase for Enzyme Catalysis in Supercritical Carbon DioxideADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 7 2007Pedro Lozano Abstract Bioreactors with covalently supported ionic liquid phases (SILP) were prepared as polymeric monoliths based on styrene,divinylbenzene or 2-hydroxyethyl methacrylate,ethylene dimethacrylate, and with imidazolium units loadings ranging from 54.7 to 39.8,% wt IL per gram of polymer. The SILPs were able to absorb Candida antarctica lipase B (CALB), leading to highly efficient and robust heterogeneous biocatalysts. The bioreactors were prepared as macroporous monolithic mini-flow systems and tested for the continuous flow synthesis of citronellyl propionate in supercritical carbon dioxide (scCO2) by transesterification. The catalytic activity of these mini-flow-bioreactors remained practically unchanged for seven operational cycles of 5,h each in different supercritical conditions. The best results were obtained when the most hydrophobic monolith, M-SILP- 8 -CALB, was assayed at 80,°C and 10,MPa, reaching a total turnover number (TON) of 35.8×104 mol product/mol enzyme. The results substantially exceeded those obtained for packed-bed reactors with supported silica-CALB-Si-4 catalyst under the same experimental conditions. [source] Interracial and Intraracial Patterns of Mate Selection Among America's Diverse Black PopulationsJOURNAL OF MARRIAGE AND FAMILY, Issue 3 2006Christie D. Batson Despite recent immigration from Africa and the Caribbean, Blacks in America are still viewed as a monolith in many previous studies. In this paper, we use newly released 2000 census data to estimate log-linear models that highlight patterns of interracial and intraracial marriage and cohabitation among African Americans, West Indians, Africans, and Puerto Rican non-Whites, and their interracial marriage and cohabitation with Whites. Based on data from several metropolitan areas, our results show that, despite lower socioeconomic status, native-born African Americans are more likely than other Blacks to marry Whites; they also are more likely to marry other Black ethnics. West Indians, Africans, and Puerto Rican non-Whites are more likely to marry African Americans than to marry Whites. Interracial relationships represent a greater share of cohabiting unions than marital unions. The majority of interracial unions, including native and immigrant Blacks, consist of a Black man and White woman. The implications for marital assimilation are discussed. [source] Sheathless electrospray ionization directly from a capillary monolith for fast liquid chromatography coupled to Fourier transform ion cyclotron resonance mass spectrometryJOURNAL OF MASS SPECTROMETRY (INCORP BIOLOGICAL MASS SPECTROMETRY), Issue 2 2004Felix C. Leinweber [source] Rapid production of a plasmid DNA encoding a malaria vaccine candidate via amino-functionalized poly(GMA- co -EDMA) monolithAICHE JOURNAL, Issue 11 2008Michael K. Danquah Abstract Malaria is a global health problem; an effective vaccine is urgently needed. Due to the relative poverty and lack of infrastructure in malaria endemic areas, DNA-based vaccines that are stable at ambient temperatures and easy to formulate have great potential. While attention has been focused mainly on antigen selection, vector design and efficacy assessment, the development of a rapid and commercially viable process to manufacture DNA is generally overlooked. We report here a continuous purification technique employing an optimized stationary adsorbent to allow high-vaccine recovery, low-processing time, and, hence, high-productivity. A 40.0 mL monolithic stationary phase was synthesized and functionalized with amino groups from 2-Chloro-N,N-diethylethylamine hydrochloride for anion-exchange isolation of a plasmid DNA (pDNA) that encodes a malaria vaccine candidate, VR1020-PyMSP4/5. Physical characterization of the monolithic polymer showed a macroporous material with a modal pore diameter of 750 nm. The final vaccine product isolated after 3 min elution was homogeneous supercoiled plasmid with gDNA, RNA and protein levels in keeping with clinical regulatory standards. Toxicological studies of the pVR1020-PyMSP4/5 showed a minimum endotoxin level of 0.28 EU/mg pDNA. This cost-effective technique is cGMP compatible and highly scalable for the production of DNA-based vaccines in commercial quantities, when such vaccines prove to be effective against malaria. © 2008 American Institute of Chemical Engineers AIChE J, 2008 [source] Rapid lightoff of syngas production from methane: A transient product analysisAICHE JOURNAL, Issue 1 2005Kenneth A. Williams Abstract Steady-state production of syngas (CO and H2) can be attained within 10 s from room-temperature mixtures of methane and air fed to a short-contact-time reactor by initially operating at combustion stoichiometry (CH4/O2 = 0.5) and then quickly switching to syngas stoichiometry (CH4/O2 = 2.0). The methane/air mixture is first ignited, forming a premixed flame upstream of the catalyst that heats the Rh-impregnated ,-alumina foam monolith to catalytic lightoff (T > 500°C) in a few seconds. The methane/oxygen ratio is then increased to partial oxidation stoichiometry, which extinguishes the flame and effects immediate autothermal syngas production. Transient species profiles are measured with a rapid-response mass spectrometer (response time constant , 0.5 s), and catalyst temperature is measured with a thermocouple at the catalyst back face. Because the monolith thermal response time (, 1 s) is several orders of magnitude larger than the reaction timescales (, 10,12 to 10,3 s), chemistry and flow should be mathematically decoupled from local transient variations in catalyst temperature. Using this assumption, a transient temperature profile is combined with detailed surface chemistry for methane on Rh in a numerical plug-flow model. This approach accurately reproduces the transient species profiles measured during experimental lightoff for short combustion time experiments and lends insight into how the monolith temperature develops with time. The combined experimental and numerical efforts supply useful information on the transient reactor behavior for various combustion times and identify a combustion time to avoid undershoot or overshoot in catalyst temperature and minimize start-up time. © 2004 American Institute of Chemical Engineers AIChE J, 51: 247,260, 2005 [source] Preparing titania aerogel monolithic chromatography columns using supercritical carbon dioxideJOURNAL OF SEPARATION SCIENCE, JSS, Issue 11 2010Ruohong Sui Abstract The search for a method to fabricate monolithic inorganic columns has attracted significant recent attention due to their unique ability in separation applications of various biomolecules. Silica and polymer based monolithic columns have been prepared, but titania and other metal oxide monoliths have been elusive, primarily due to their fragility. This article describes a new approach for preparing nanostructured titania based columns, which offer better performance over conventional particle packed columns for separating a wide variety of biomolecules including phosphopeptides. TiO2 monolithic aerogels were synthesized in separation columns using in situ sol-gel reactions in supercritical carbon dioxide (scCO2) followed by calcination, and compared to those prepared in heptanes. The characterization results show that scCO2 is a better solvent for the sol-gel reactions, providing lower shrinkage with the anatase TiO2 monolith composed of nanofibers with very high surface areas. The monolithic columns show the ability to isolate phosphopeptides with little flow resistance compared to conventional titania particle based microcolumns. [source] Preparation, characterisation and modification of carbon-based monolithic rods for chromatographic applicationsJOURNAL OF SEPARATION SCIENCE, JSS, Issue 9 2010Ali H. Eltmimi Abstract A range of porous carbon-based monolithic (PCM) rods with flow-through pore sizes of 1, 2, 5 and 10,,m, were produced using a silica particle template method. The rods were characterised using SEM and energy-dispersive X-ray spectroscopy, BET surface area and porous structure analysis, dilatometry and thermal gravimetry. SEM evaluation of the carbon monolithic structures revealed an interconnected rigid bimodal porous structure and energy-dispersive X-ray spectroscopy analysis verified the quantitative removal of the embedded silica beads. The specific surface areas of the 1, 2, 5 and 10,,m rods were 178, 154, 84 and 125,m2/g after pyrolysis and silica removal, respectively. Shrinkage of the monolithic rods during pyrolysis is proportional to the particle size of the silica used and ranged from 9 to 12%. Mercury porosimetry showed a narrow distribution of pore sizes, with an average of ,700,nm for the 1,,m carbon monolith. The suitability of bare and surface oxidised PCM rods for the use as a stationary phase for reversed and normal phase LC was explored. The additional modification of PCM rods with gold micro-particles followed by 6-mercaptohexanoic acid was performed and ion-exchange properties were evaluated. [source] | ||||||||||||||||||||||||||||||||||||||||