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Nitrogen Sorption Analysis (nitrogen + sorption_analysis)
Selected AbstractsInfluence of Surface Chemistry on Dehydrogenation in Carbon Cryogel Ammonia Borane NanocompositesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 5 2009Saghar Sepehri Abstract This paper reports the synthesis and characterization of boron- and nitrogen-modified carbon cryogel (CC) ammonia borane (AB) nanocomposites (BNCC-AB) for hydrogen storage. Resorcinol,formaldehyde (RF) derived CCs were modified by homogeneous dispersion of AB in RF hydrogel prior to pyrolysis. Nanocomposites were fabricated by immersing CC in the AB solution. Nitrogen sorption analysis, X-ray photoelectron spectroscopy, and differential scanning calorimetry at multiple heating rates were used to study the structure and dehydrogenation properties of the nanocomposites. The results demonstrated lower dehydrogenation temperatures and reduced activation energies for AB when confined inside pores of B- and N-modified CCs relative to AB when confined in the unmodified CC with the same pore size.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Temperature Responsive Solution Partition of Organic,Inorganic Hybrid Poly(N -isopropylacrylamide)-Coated Mesoporous Silica Nanospheres,ADVANCED FUNCTIONAL MATERIALS, Issue 9 2008Po-Wen Chung Abstract A series of poly(N -isopropylacrylamide)-coated mesoporous silica nanoparticle materials (PNiPAm-MSNs) has been synthesized by a surface-initiated living radical polymerization with a reversible addition,fragmentation chain transfer (RAFT) reaction. The structure and the degree of polymerization of the PNiPAm-MSNs has been characterized by a variety of techniques, including nitrogen sorption analysis, 29Si and 13C solid-state NMR spectroscopy, transmission electron microscopy (TEM), and powder X-ray diffraction (XRD). The thermally induced changes of the surface properties of these polymer-coated core,shell nanoparticles have been determined by examining their partition activities in a biphasic solution (water/toluene) at different temperatures. [source] A Study on the Effect of Template Chain Length on the Synthesis of Mesoporous Silica in An Acidic ConditionJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2007Yang Yu-Xiang Hexagonal mesoporous silica materials were synthesized in an acidic medium using different chain length of the quaternary ammonium surfactants as a template. The effects of chain length on the physical property, morphology of mesoporous materials, and the temperature on synthesis of materials in CnTMBr,TEOS,HNO3,H2O (n=12,14,16,18) system were systematically studied. The synthesized products were characterized by X-ray diffraction patterns, scanning electron microscopy, transmission electron microscopy, and nitrogen sorption analysis. It was found that degree of ordering, the d spacing values, and pore size all increase with an increase in the chain length of the template. The optimum synthesis temperature for mesoporous silica using C18TMBr,TEOS,HNO3,H2O system is slightly higher than the Krafft point. The temperature and pH can all affect the expandability of micelles, and so an increase in temperature and decrease in pH all lead to an increase in the pore size. It is also found that the shear flow and chain length are two key factors inducing the formation of millimeter-scaled silica ropes and micrometer-scaled rope fibers. [source] Effect of Counterions on Synthesis of Mesoporous Silica by the Route of TemplateJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 7 2007Yang Yu-Xiang Mesoporous silica materials with ordered hexagonal and parallel-arranged pore channel have been synthesized using cetyl trimethylammonium bromide as a template and Na2SO4 as counterions. Their ordered mesostructures were characterized by infrared spectroscopy, X-ray diffraction patterns, scanning electron microscopy, transmission electron microscopy, and nitrogen sorption analysis. The effects of Na2SO4 concentration on variations of morphology, specific surface area, and pore size were discussed; the results show that a high concentration of Na2SO4 induces the formation of crystal threads with a "tubules-within-tubule" structure, and also leads to mesoporous silica materials with spherical, fabaceous, sheet-like, or prismatic shapes. The results also show that a high concentration of Na2SO4 can make the pore size decrease, but cannot change pore wall thickness, demonstrating the stability of the hexagonal-shaped pores. [source] | ||||||||||