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Ammonium Hydroxide (ammonium + hydroxide)
Selected AbstractsDetermination of refractory organic matter in marine sediments by chemical oxidation, analytical pyrolysis and solid-state 13C nuclear magnetic resonance spectroscopyEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 3 2008J. M. De La Rosa Summary Seeking to quantify the amount of refractory organic matter (ROM), which includes black carbon-like material (BC), in marine sediments, we have applied a two-step procedure that consists of a chemical oxidation with sodium chlorite of the demineralized sediments followed by integration of the aromatic C region in the remaining residues by solid-state 13C nuclear magnetic resonance (NMR) spectroscopy. The efficacy for lignin removal was tested by analytical pyrolysis in the presence of tetramethyl ammonium hydroxide (TMAH). Riverine, estuarine and offshore marine sediment samples were collected from the southwest Atlantic coast of Spain, a site of geological and environmental interest. Measured contents of BC-like material ranged between 3.0 and 45.7% of the total organic carbon. Greater relative BC contents were found in riverine sediments close to urban areas, which show an elevated input of anthropogenic organic material. The contents of BC-like material in offshore marine sediments (5.5,6.1%) were similar to those previously reported for these kinds of samples. However, NMR and pyrolysis-GC/MS of the isolated ROM reveals that abundant refractory aliphatic organic material remains in most of the marine samples after chlorite oxidation. We suggest that this pool of aliphatic carbon may play an important role as a stable carbon pool within the global C cycle. [source] Low-Temperature Synthesis of Zinc Oxide NanoparticlesINTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 4 2006Po-Yi Wu Crystalline zinc oxide nanoparticles have been prepared by mixing aqueous solutions of zinc nitrate and hexamethylenetetramine (HMT) at 60°C and 80°C. Transmission electron microscopy and X-ray diffraction show that the ZnO nanoparticles of diameters ranging from 15,33 nm and 25,43 nm long are formed. Aspect ratio is observed to range from 1.18 to 1.74 at 60°C and 1.22 to 1.70 at 80°C as the HMT to zinc nitrate concentration ratio increases from 10 to 150. Nanoparticle size decreases as the concentration of HMT increases. Much larger ZnO particles are formed with ammonium hydroxide as a hydrolysis agent without HMT. In summary, HMT is an ammonium-hydroxide source in the reaction, a surfactant for retaining nanosize, and not necessarily a template for ZnO nucleation. [source] Preparation and use of a mesoporous silicate material for the removal of tetramethyl ammonium hydroxide (TMAH) from aqueous solutionJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 12 2001Brian P Kelleher Abstract A cubic mesoporous silicate (CMS) was prepared, characterised, and assessed as an adsorbent for tetramethyl ammonium hydroxide (TMAH) from aqueous solution. The adsorption process was studied as a function of temperature and time. Sorption closely followed the Langmuir model. The adsorption of TMAH on CMS was endothermic and kinetic studies suggest that the overall rate of adsorption was pseudo-second-order. Pore diffusion effects contribute to limiting the overall rate of adsorption while at lower initial TMAH concentrations, film diffusion becomes more important. Desorption studies were carried out using water and methanol. Methanol was the superior desorbing agent. © 2001 Society of Chemical Industry [source] Quantitative analysis of EO9 (apaziquone) and its metabolite EO5a in human plasma by high-performance liquid chromatography under basic conditions coupled to electrospray tandem mass spectrometryJOURNAL OF MASS SPECTROMETRY (INCORP BIOLOGICAL MASS SPECTROMETRY), Issue 10 2006Liia D. Vainchtein A sensitive and specific LC-MS/MS assay for the quantitative determination of EO9 and its metabolite EO5a is presented. A 200-µl human plasma aliquot was spiked with a mixture of deuterated internal standards EO9- d3 and EO5a- d4 and extracted with 1.25 ml ethyl acetate. Dried extracts were reconstituted in 0.1 M ammonium acetate,methanol (7 : 3, v/v) and 25 µl-volumes were injected into the HPLC system. Separation was achieved on a 150 × 2.1 mm C18 column using an alkaline eluent (1 mM ammonium hydroxide,methanol (gradient system)). Detection was performed by positive ion electrospray followed by tandem mass spectrometry. The assay quantifies a range from 5 to 2500 ng/ml for EO9 and from 10 to 2500 ng/ml EO5a using 200 µl of human plasma samples. Validation results demonstrate that EO9 and EO5a concentrations can be accurately and precisely quantified in human plasma. This assay will be used to support clinical pharmacologic studies with EO9. Copyright © 2006 John Wiley & Sons, Ltd. [source] Preparation and characterization of polymethacrylate monolithic capillary columns with dual hydrophilic interaction reversed-phase retention mechanism for polar compoundsJOURNAL OF SEPARATION SCIENCE, JSS, Issue 15-16 2009í Urban Abstract Monolithic columns for capillary hydrophilic interaction liquid chromatography (HILIC) were prepared in fused-silica capillaries by radical co-polymerization of [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide and ethylene dimethacrylate in various binary and ternary porogen solvent mixtures with azobisisobutyronitrile as the initiator of the polymerization reaction. Columns showed mixed separation modes: reversed-phase (RP) in water-rich mobile phases and HILIC at high concentrations of acetonitrile (>60,80%) in aqueous,organic mobile phases. A continuous change in retention was observed at increasing concentration of water in acetonitrile, giving rise to characteristic U-turn plots of retention factors versus the concentration of water in the mobile phase, with minima corresponding to the transition between the mechanisms controlling the retention. The selectivity of organic polymer monolithic columns for HILIC separations can be varied by adjusting the concentration of sulfobetaine monomer and the composition of the porogen solvent in the polymerization mixture. Under HILIC conditions, the monolithic capillary sulfobetaine columns show separation selectivities for polar phenolic acids similar to those of a commercial silica-based sulfobetaine ZIC-HILIC column, which, however, has limited selectivity in the RP mode due to lower retention. [source] Electrical Conductivity of Submicrometer Gadolinia-Doped Ceria Sintered at 1000°C Using Precipitation-Synthesized Nanocrystalline PowdersJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2008Pandurangan Muralidharan A simple synthetic strategy has been implemented to obtain low-temperature sintered fine grain size gadolinia-doped ceria, Ce0.9Gd0.1O1.95, (CGO) electrolyte pellets with a high density using weakly agglomerated particles of calcined nanopowders synthesized by a homogeneous precipitation process. The precipitants used were diethylamine (DEA process) and ammonium hydroxide in neutral precipitation (NP process). X-ray diffraction patterns revealed the single-phase crystalline CGO of a fluorite-type structure. The crystalline powder was directly synthesized from solution by the DEA process at room temperature, whereas the NP process powder was crystallized upon hydrothermal treatment at an elevated temperature. Transmission electron microscopy images showed homogeneously dispersed spherical-shaped particles of ,5 nm size for nanopowders calcined at 300°C for 4 h. A high densification range from ,96% to 99% of the theoretical was achieved for the nonconventionally low-temperature sintered pellets at 1000°C from weakly bonded particles of CGO nanopowders calcined at 300°C for 4 h without any sintering aid. The dense CGO pellets sintered at 1000°C for 4 h with an average grain size of ,150,300 nm exhibited a promising high electrical conductivity of 2.03 × 10,2 S/cm (DEA process) and 2.17 × 10,2 S/cm (NP process), measured at 650°C, and low activation energy Ea. The electrical conductivities of fine grain size low-temperature sintered CGO pellets are comparable with the literature reports of sintered pellets using sintering aids, and high-temperature sintered CGO pellets above 1300°C with a larger grain size. [source] The preparation of MnZn-ferrite nanoparticles in a water/CTAB, 1-butanol/1-hexanol reverse microemulsionPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 12 2004Abstract Manganese zinc ferrite nanoparticles were prepared using a precipitation in reverse microemulsion system consisting of hexadecyltrimethyl ammonium bromide (CTAB) as a surfactant, 1-butanol as a co-surfactant, 1-hexanol as an oil phase and an aqueous solution of metal sulfates. Tetramethyl ammonium hydroxide (TMAH) served as the precipitating agent. The influence of the microemulsion's composition on the nature of the spinel product was studied. The synthesized nanoparticles were characterized using transmission electron microscopy (TEM), X-ray diffractometry (XRD), specific surface area (BET) and magnetometry. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] DNA AND PROTEIN RECOVERY FROM WASHED EXPERIMENTAL STONE TOOLS,ARCHAEOMETRY, Issue 4 2004O. C. SHANKS Traces of protein and DNA are preserved on stone tools used to process animals. Previous research documents the identification of protein residues from tools sonicated in 5% ammonium hydroxide, but it remains untested whether the same treatment yields useable DNA. In this study we report both DNA and protein recovery using 5% ammonium hydroxide from residues on stone tools. We extracted 13-year-old residues from experimentally manufactured stone tools used to butcher a single animal. We also show that surface washing procedures typically used to curate stone tools remove only a small fraction of the DNA and protein deposited during animal butchery. [source] Solid-Based Hydrothermal Synthesis and Characterization of Alumina Nanofibers with Controllable Aspect RatiosJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 6 2009Shou-Cang Shen Nanofibers of AlOOH with controllable aspect ratios have been synthesized by a facile steam-assisted solid-phase crystallization route. The morphology and aspect ratios of resulting AlOOH nanofibers were significantly influenced by the alkaline medium used in the preparation of solid precipitates from Al(NO3)3 solution. When tetramethylammonium hydroxide was used for precipitation, straight rod-like nanofibers with aspect ratios of 10,20 were obtained. The use of other tetra-alkylated ammonium hydroxides, such as tetraethylammonium hydroxide, tetrapropylammonium hydroxide or tetrabutylammonium hydroxide, led to the formation of long wire-like nanofibers with aspect ratios up to 150. After thermal treatment at 600°C, the morphologies of the one-dimensional nanostructures were well preserved while the crystal structure was converted to ,-alumina. The wire-like nanofibers of alumina possessed higher thermal stability than alumina nanorods, and both exhibited much higher stability as compared with alumina micropowder. [source] | |||||||||||||