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Selective Adsorption (selective + adsorption)
Selected AbstractsSelective Adsorption of Polychlorinated Dibenzo- p -dioxins and Dibenzofurans by the Zeosils UTD-1, SSZ-24, and ITQ-4CHEMISTRY - A EUROPEAN JOURNAL, Issue 1 2004Ralph Jäger Dr. Abstract Zeosils are microporous solids with a pure silica framework. Due to their hydrophobic properties, zeosils are ideal host materials for the adsorption of hydrophobic guest molecules. We tested zeosils with different pore diameters (UTD-1, SSZ-24 and ITQ-4 as well as CIT-5) for the selective adsorption of the polychlorinated dibenzo- p -dioxins and dibenzofurans. This group of highly toxic substances contains 210 congeners that possess similar chemical properties, but differ in their size and shape. In the experiment, polychlorinated dibenzo- p -dioxins and dibenzofurans were extracted from fly ash of a waste incinerator, adsorbed on amorphous silica, then thermally desorbed and flushed over a sequential arrangement of the zeosils at elevated temperature by a stream of nitrogen. ITQ-4 with the smallest pore diameter was placed first, followed by SSZ-24 and, finally, by UTD-1 with the largest pore diameter. After the experiment, the zeosils were analysed for their contents of the different congeners. The results show that the sorption of the congeners occurs selectively and that it is governed by the size and the shape of the dioxin molecules, which in turn depend on the number of chlorine atoms and the pattern of chlorine substitution (regioisomers). Geometrical reasoning as well as molecular dynamics calculations on the zeosil structures and on the dioxin molecules were helpful in rationalising the results. This work represents an especially complex case of the molecular sieving effect and may lead to a selective on-line monitoring of the concentrations of dioxin molecules in waste gases of industrial combustion processes. The size- and shape-selective sorption of dioxin molecules may also bear some resemblance to the molecular recognition process that occurs in nature at the aryl hydrocarbon receptor. [source] Fabrication of a Memory Chip by a Complete Self-Assembly Process Using State-of-the-Art Multilevel Cell (MLC) Technology,ADVANCED FUNCTIONAL MATERIALS, Issue 8 2008Anirban Bandyopadhyay Abstract Using a two bit molecular switch, an ultra-dense memory chip has been built following a fully automated fabrication process. Well-ordered templates are grown naturally using a well-defined protocol of temperature variation. This template is so designed that molecules are adsorbed selectively only into particular sites whenever they are bombarded on the template through an e-beam evaporator for a particular time. The technique is a generalized protocol that has been used to grow atomic-scale templates by proper tuning of basic global parameters like temperature and evaporation time. Tuning of the basic template parameters is also demonstrated here, and has been used to scale down parameter values following the same route. Tuning the junction profile should allow selective adsorption of more complicated multi-level switches in future. Therefore, a fairly simple technology has been established that addresses one of the most fundamental issues of continuous miniaturization, i.e., simultaneous automated growth of thousands of atomically precise single molecular devices. [source] The Synthesis of Novel Porous Functional Materials for use as Nitrosamine Traps,ADVANCED FUNCTIONAL MATERIALS, Issue 11 2004Y. Xu Abstract Two novel porous nitrosamine traps have been synthesized in order to eliminate carcinogens from the environment. A functional mesoporous material, CuO/SBA-15, has been synthesized by using an in-situ coating method, with the addition of a guest salt to the reaction system to modify the porous materials before the particles of SBA-15 were incubated; the synthesis and modification processes were performed in a single step. The resulting mesoporous composites selectively adsorb N -nitrosopyrrolidine (NPYR), a typical volatile nitrosamine, and are potential cigarette additives that can be used for the removal of nitrosamines from cigarette smoke, thereby protecting public health and the environment. In another reaction, silica gel is modified by being coated with magnesia and then corroded by NaOH solution. The magnesia is dispersed onto the silica by impregnating it with a magnesium acetate solution, followed by calcination. After corrosion of the calcined sample with caustic soda, only the silica particles that are completely covered by magnesia remain. This material exhibits a similar ability to SBA-15 and zeolite NaY in its selective adsorption of NPYR. [source] Polymer-Controlled Crystallization of Unique Mineral SuperstructuresADVANCED MATERIALS, Issue 4 2010Shao-Feng Chen Abstract The origin of complex superstructures of biomaterials in biological systems and the amazing self-assembly mechanisms of their emergence have attracted a great deal of attention recently. Mimicking nature, diverse kinds of hydrophilic polymers with different functionalities and organic insoluble matrices have been designed for the morphogenesis of inorganic crystals. In this Research News, emerging new strategies for morphogenesis and controlled crystal growth of minerals, that is, selective adsorption and mesoscale transformation for highly ordered superstructures, the combination of a synthetic hydrophilic polymer with an insoluble matrix, a substrate, or the air/solution interface, and controlled crystallization in a mixed solvent are highlighted. It is shown that these new strategies can be even further extended to morphogenesis and controlled crystallization of diverse inorganic or inorganic,organic hybrid materials with structural complexity, structural specialties, and improved functionalities. [source] Raman spectroscopy and molecular simulation investigations of adsorption on the surface of single-walled carbon nanotubes and nanospheresJOURNAL OF RAMAN SPECTROSCOPY, Issue 6 2007Maher S. Amer Abstract Raman spectroscopy has, for long, been utilized to investigate material systems on the micro and mesoscales. Recently, the technique has proven its ability in exploring systems on the nanoscale. In this paper, we review our recent work on the Raman investigation of molecular adsorption from liquid mixtures on surfaces of single-walled carbon nanotubes and fullerene nanospheres, emphasizing the following major research findings: the development of a Raman-based technique capable of sensing local chemical interactions on the surface of carbon nanotubes and spheres; the molecular simulation results supporting the Raman investigation; the possibility of creating mesostructures based upon mixtures of carbon nanotubes and nanospheres that are crucial for selective adsorption. The current findings represent a major new thrust for the development of new nanostructured materials with superior adsorption capabilities and unique applications. Copyright © 2007 John Wiley & Sons, Ltd. [source] Evaluation of sulfobetaine-type polymer resin as an SPE adsorbent in the analysis of trace tetracycline antibiotics in honeyJOURNAL OF SEPARATION SCIENCE, JSS, Issue 21 2009Tomoyasu Tsukamoto Abstract A new sulfobetaine polymer resin SPE method combined with HPLC-MS/MS for the determination of tetracycline (TC) antibiotics residues from honey samples is presented. The sulfobetaine resin was synthesized and was packed into a syringe-type tube, which served as the SPE cartridge for selective adsorption of TCs. TCs were quantitatively adsorbed on the sulfobetaine cartridge, when the loading solvent was 95%,v/v acetonitrile solution, and TCs adsorbed were not eluted by aqueous acetonitrile washing solution. TFA aqueous solution was used for eluting the adsorbed TCs. The proposed SPE method has been applied to the determination of TCs in honey samples. The recoveries of TCs spiked in honey samples ranged from 70 to 80%. Reduction of the recoveries might be derived from low solubility of TCs in acetonitrile. Compared with other SPE resins, this resin was superior in terms of selectivity with simple pretreatment. [source] From Trifluoroacetate Complex Precursors to Monodisperse Rare-Earth Fluoride and Oxyfluoride Nanocrystals with Diverse Shapes through Controlled Fluorination in Solution PhaseCHEMISTRY - A EUROPEAN JOURNAL, Issue 8 2007Xiao Sun Abstract We report the first systematic synthesis of monodisperse rare-earth (RE=La to Lu, Y) fluoride and oxyfluoride nanocrystals with diverse shapes (trigonal REF3 triangular, truncated-triangular, hexagonal, and polygonal nanoplates; orthorhombic REF3 quadrilateral and zigzag-shaped nanoplates; cubic REOF nanopolyhedra and nanorods) from single-source precursors (SSP) of [RE(CF3COO)3] through controlled fluorination in oleic acid (OA)/oleylamine (OM)/1-octadecene (ODE). To selectively obtain REF3 or REOF nanocrystals, the fluorination of the REO bond to the REF bond at the nucleation stage was controlled by finely tuning the ratio of OA/ODE or OA/OM, and the reaction temperature. For phase-pure REF3 or REOF naocrystals, their shape-selective syntheses could be realized by further modifying the reaction conditions. The two-dimensional growth of the REF3 nanoplates and the one-dimensional growth of the REOF nanorods were likely due to the selective adsorption of the capping ligands on specific crystal planes of the nanocrystals. Those well-shaped nanocrystals with diverse geometric symmetries (such as D3h, D6h, C2h, Oh, and Dnh) displayed a remarkable capability to form self-assembled superlattices. By manipulating the solvent,substrate combination, the plate-shaped REF3 nanocrystals could form highly ordered nanoarrays by means of either the face-to-face formation or the edge-to-edge formation. By using this SSP strategy, we also obtained high-quality LaF3:Eu and LaF3:Eu/LaF3 triangular nanoplates that showed photoluminescent red emissions of Eu3+ ions sensitive to the surface effect. [source] Selective Adsorption of Polychlorinated Dibenzo- p -dioxins and Dibenzofurans by the Zeosils UTD-1, SSZ-24, and ITQ-4CHEMISTRY - A EUROPEAN JOURNAL, Issue 1 2004Ralph Jäger Dr. Abstract Zeosils are microporous solids with a pure silica framework. Due to their hydrophobic properties, zeosils are ideal host materials for the adsorption of hydrophobic guest molecules. We tested zeosils with different pore diameters (UTD-1, SSZ-24 and ITQ-4 as well as CIT-5) for the selective adsorption of the polychlorinated dibenzo- p -dioxins and dibenzofurans. This group of highly toxic substances contains 210 congeners that possess similar chemical properties, but differ in their size and shape. In the experiment, polychlorinated dibenzo- p -dioxins and dibenzofurans were extracted from fly ash of a waste incinerator, adsorbed on amorphous silica, then thermally desorbed and flushed over a sequential arrangement of the zeosils at elevated temperature by a stream of nitrogen. ITQ-4 with the smallest pore diameter was placed first, followed by SSZ-24 and, finally, by UTD-1 with the largest pore diameter. After the experiment, the zeosils were analysed for their contents of the different congeners. The results show that the sorption of the congeners occurs selectively and that it is governed by the size and the shape of the dioxin molecules, which in turn depend on the number of chlorine atoms and the pattern of chlorine substitution (regioisomers). Geometrical reasoning as well as molecular dynamics calculations on the zeosil structures and on the dioxin molecules were helpful in rationalising the results. This work represents an especially complex case of the molecular sieving effect and may lead to a selective on-line monitoring of the concentrations of dioxin molecules in waste gases of industrial combustion processes. The size- and shape-selective sorption of dioxin molecules may also bear some resemblance to the molecular recognition process that occurs in nature at the aryl hydrocarbon receptor. [source] Can Metal,Organic Framework Materials Play a Useful Role in Large-Scale Carbon Dioxide Separations?CHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 8 2010Seda Keskin Dr. Abstract Metal,organic frameworks (MOFs) are a fascinating class of crystalline nanoporous materials that can be synthesized with a diverse range of pore dimensions, topologies, and chemical functionality. As with other well-known nanoporous materials, such as activated carbon and zeolites, MOFs have potential uses in a range of chemical separation applications because of the possibility of selective adsorption and diffusion of molecules in their pores. We review the current state of knowledge surrounding the possibility of using MOFs in large-scale carbon dioxide separations. There are reasons to be optimistic that MOFs may make useful contributions to this important problem, but there are several critical issues for which only very limited information is available. By identifying these issues, we provide what we hope is a path forward to definitively answering the question posed in our title. [source] | |||||||||||||