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Relevant bibliographies by topics / Metal hydroxides; High resolution

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Academic literature on the topic 'Metal hydroxides; High resolution'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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Journal articles on the topic "Metal hydroxides; High resolution"

1

Arrigo, Rosa, and Manfred Schuster. "On the High Structural Heterogeneity of Fe-Impregnated Graphitic-Carbon Catalysts from Fe Nitrate Precursor." Catalysts 9, no. 4 (March 27, 2019): 303. http://dx.doi.org/10.3390/catal9040303.

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Wet impregnation is broadly applied for the synthesis of carbon-supported metal/metal oxide nanostructures because of its high flexibility, simplicity and low cost. By contrast, impregnated catalysts are typified by a usually undesired nanostructural and morphological heterogeneity of the supported phase resulting from a poor stabilization at the support surface. This study on graphite-supported Fe-based materials from an Fe nitrate precursor is concerned with the understanding of the chemistry that dictates during the multistep synthesis, which is key to designing structurally homogeneous catalysts. By means of core-level X-ray photoelectron spectroscopy, near-edge X-ray absorption fine structure spectroscopy and atomic resolution electron microscopy, we found not only a large variety of particles sizes and morphologies but also chemical phases. Herein, thermally stable single atoms and few atoms clusters are identified together with large agglomerates of an oxy-hydroxide ferrihydrite-like phase. Moreover, the thermally induced phase transformation of the initially poorly ordered oxy-hydroxide phase into several oxide phases is revealed, together with the existence of thermally stable N impurities retained in the structure as Fe–N–O bonds. The nature of the interactions with the support and the structural dynamics induced by the thermal treatment rationalize the high heterogeneity observed in these catalysts.

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Case, C. Patrick, Lyndon Ellis, Justine C. Turner, and Ben Fairman. "Development of a Routine Method for the Determination of Trace Metals in Whole Blood by Magnetic Sector Inductively Coupled Plasma Mass Spectrometry with Particular Relevance to Patients with Total Hip and Knee Arthroplasty." Clinical Chemistry 47, no. 2 (February 1, 2001): 275–80. http://dx.doi.org/10.1093/clinchem/47.2.275.

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Abstract Background: Joint-replacement surgery has revolutionized the treatment of osteoarthritis and is still the most effective therapy. A recent clinical trend reintroducing metal-on-metal bearing surfaces has in turn stimulated a requirement for accurate measurement of the concentrations of relevant metals in both pre- and postoperative patients. Thus, there is a need for cost-effective, multielement methods for trace metal analysis in whole blood to monitor possible increases in wear metal concentrations. Methods: A method was developed to allow routine analysis of whole blood samples for molybdenum, cobalt, chromium, and nickel. Sample preparation consisted of a simple 1:10 dilution of whole blood with a solution of 10 mL/L Triton X-100, 0.0002 mol/L EDTA, and 0.01 mol/L ammonium hydroxide. Final determination was performed by a double-focusing magnetic sector inductively coupled plasma mass spectrometer operated in medium-resolution mode (resolution, 3400). Online addition of rhodium was used for internal standardization. Results: Detection limits in whole blood were 0.06 μg/L for chromium, cobalt, and molybdenum and 0.30 μg/L for nickel. Base concentrations of 0.22, 0.17, 0.62, and 0.99 μg/L for chromium, cobalt, molybdenum, and nickel, respectively, in whole blood have been found. Polyatomic interferences on all four elements have been shown to be resolved from the analyte masses by use of a resolution of >3000. Conclusions: The simple, rapid method of sample preparation is effective in minimizing potential contamination and enables 60 samples (run time, 8 h) to be analyzed before cleaning the instrument is necessary. A resolution >3000 was sufficient to separate polyatomic interferences from the masses of interest. The method was used to analyze a large number of blood samples taken from primary patients awaiting total hip arthroplasty. The method is sensitive enough to provide base concentrations for chromium, cobalt, and molybdenum in whole blood. The results for nickel were compromised by high signals for blank samples.

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Kemmitt, Tim, and William Henderson. "A New Route to Silicon Alkoxides from Silica." Australian Journal of Chemistry 51, no. 11 (1998): 1031. http://dx.doi.org/10.1071/c98060.

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A novel route to tetraethoxysilane and other silicon alkoxides is described, from amorphous silica (SiO2.nH2O) as the raw material. The reaction of amorphous silica with triethanolamine is enhanced by using an alkali metal hydroxide catalyst, to form a range of triethanolamine-substituted silatrane species. These can undergo alkoxide exchange in acidic alcohols to form alkoxysilatranes, tetraalkoxysilanes, hexaalkoxydisiloxanes and higher siloxanes. Reaction of triethanolamine-substituted silatranes with acetic anhydride produces acetoxysilatrane. Products were identified by multinuclear (1H, 13C and 29Si) magnetic resonance spectroscopy, electrospray mass spectrometry or high-resolution gas chromatography electron impact mass spectrometry.

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Kawaguchi, Shogo, Michitaka Takemoto, Hideki Tanaka, Shotaro Hiraide, Kunihisa Sugimoto, and Yoshiki Kubota. "Fast continuous measurement of synchrotron powder diffraction synchronized with controlling gas and vapour pressures at beamline BL02B2 of SPring-8." Journal of Synchrotron Radiation 27, no. 3 (March 16, 2020): 616–24. http://dx.doi.org/10.1107/s1600577520001599.

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A gas- and vapour-pressure control system synchronized with the continuous data acquisition of millisecond high-resolution powder diffraction measurements was developed to study structural change processes in gas storage and reaction materials such as metal organic framework compounds, zeolite and layered double hydroxide. The apparatus, which can be set up on beamline BL02B2 at SPring-8, mainly comprises a pressure control system of gases and vapour, a gas cell for a capillary sample, and six one-dimensional solid-state (MYTHEN) detectors. The pressure control system can be remotely controlled via developed software connected to a diffraction measurement system and can be operated in the closed gas and vapour line system. By using the temperature-control system on the sample, high-resolution powder diffraction data can be obtained under gas and vapour pressures ranging from 1 Pa to 130 kPa in temperatures ranging from 30 to 1473 K. This system enables one to perform automatic and high-throughput in situ X-ray powder diffraction experiments even at extremely low pressures. Furthermore, this developed system is useful for studying crystal structures during the adsorption/desorption processes, as acquired by millisecond and continuous powder diffraction measurements. The acquisition of diffraction data can be synchronized with the control of the pressure with a high frame rate of up to 100 Hz. In situ and time-resolved powder diffraction measurements are demonstrated for nanoporous Cu coordination polymer in various gas and vapour atmospheres.

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Chitrakar, Iva, Syed Fardin Ahmed, Andrew T. Torelli, and Jarrod B. French. "Structure of the E. coli agmatinase, SPEB." PLOS ONE 16, no. 4 (April 15, 2021): e0248991. http://dx.doi.org/10.1371/journal.pone.0248991.

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Agmatine amidinohydrolase, or agmatinase, catalyzes the conversion of agmatine to putrescine and urea. This enzyme is found broadly across kingdoms of life and plays a critical role in polyamine biosynthesis and the regulation of agmatine concentrations. Here we describe the high-resolution X-ray crystal structure of the E. coli agmatinase, SPEB. The data showed a relatively high degree of pseudomerohedral twinning, was ultimately indexed in the P31 space group and led to a final model with eighteen chains, corresponding to three full hexamers in the asymmetric unit. There was a solvent content of 38.5% and refined R/Rfree values of 0.166/0.216. The protein has the conserved fold characteristic of the agmatine ureohydrolase family and displayed a high degree of structural similarity among individual protomers. Two distinct peaks of electron density were observed in the active site of most of the eighteen chains of SPEB. As the activity of this protein is known to be dependent upon manganese and the fold is similar to other dinuclear metallohydrolases, these peaks were modeled as manganese ions. The orientation of the conserved active site residues, in particular those amino acids that participate in binding the metal ions and a pair of acidic residues (D153 and E274 in SPEB) that play a role in catalysis, are similar to other agmatinase and arginase enzymes and is consistent with a hydrolytic mechanism that proceeds via a metal-activated hydroxide ion.

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Hemmati, Shohreh, Erin Retzlaff-Roberts, Corren Scott, and Michael T. Harris. "Artificial Sweeteners and Sugar Ingredients as Reducing Agent for Green Synthesis of Silver Nanoparticles." Journal of Nanomaterials 2019 (January 21, 2019): 1–16. http://dx.doi.org/10.1155/2019/9641860.

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An environmentally friendly technique has been developed to produce metal nanoparticles using green synthesis methods. In this study, silver nanostructures were synthesized using different sugar substitutes and artificial sweeteners as green reducing agents in an aqueous solution at low temperature. The main ingredients (such as maltodextrin, sucrose, saccharin, and sucralose) of the artificial sweeteners acting as reducing agents were used to reduce Ag+ ions to Ag0. The pH of the solution was controlled during synthesis through the addition of sodium hydroxide (NaOH) to increase the strength of the reducing agents by converting nonreducing sugars to reducing ones and consequently increasing the rate of silver nanoparticle formation. The size and morphology of the synthesized nanostructures were characterized by transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX). The formation of nanostructures during the course of the reactions was investigated by UV-visible (UV-vis) spectroscopy characterization of an aliquot of sample at specific intervals. The function of each artificial sweetener and corresponding ingredients as a reducing agent and capping agent was investigated by Fourier-transform infrared spectroscopy (FTIR) and mass spectrometry (MS).

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Li, Mengxue, Jianyong Liu, Yunfeng Xu, and Guangren Qian. "Phosphate adsorption on metal oxides and metal hydroxides: A comparative review." Environmental Reviews 24, no. 3 (September 2016): 319–32. http://dx.doi.org/10.1139/er-2015-0080.

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Phosphorus removal from wastewater is important for eutrophication control of water bodies. Metal oxides and metal hydroxides have always been developed and investigated for phosphorus removal, because of their abundance, low cost, environmental friendliness, and chemically stability. This paper presents a comparative review of the literature on the preparation methods, adsorption behaviors, adsorption mechanisms, and the regeneration of metal (hydr)oxides (e.g., Fe, Zn, Al, etc.) with regard to phosphate removal. The contrasting results showed that metal hydroxides could offer an effective and economic alternative to metal oxides, because of their cost–benefit synthesis methods, higher adsorption capacities, and shorter adsorption equilibrium times. However, the specific surface area of metal oxides is larger than that of metal hydroxides because of the calcination process. Metal oxides with a higher pH at the zero point of charge have wider optimal adsorption pH ranges than metal hydroxides because of their surface precipitation in alkaline solutions. The regeneration of metal oxides using acids, bases, and salts and that of metal hydroxides using acids and bases has been critically examined. Further research on uniform metal (hydr)oxides with small particle size, high stabilities, low cost, and that are easily regenerated with promising desorbents are proposed. In addition, quantitative mechanism study and application in continuous-mode column trials are also suggested.

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Sill, Claude W. "Precipitation of actinides as fluorides or hydroxides for high-resolution alpha spectrometry." Nuclear and Chemical Waste Management 7, no. 3-4 (January 1987): 201–15. http://dx.doi.org/10.1016/0191-815x(87)90066-0.

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Zhao, Zehao, Kaichang Kou, Limin Zhang, and Hongjing Wu. "High efficiency electromagnetic wave absorber derived from transition metal layered double hydroxides." Journal of Colloid and Interface Science 579 (November 2020): 733–40. http://dx.doi.org/10.1016/j.jcis.2020.06.123.

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Blanc, J., M. Broyer, J. Chevaleyre, Ph Dugourd, H. K�hling, P. Labastie, M. Ulbricht, J. P. Wolf, and L. W�ste. "High resolution spectroscopy of small metal clusters." Zeitschrift f�r Physik D Atoms, Molecules and Clusters 19, no. 1-4 (March 1991): 7–12. http://dx.doi.org/10.1007/bf01448245.

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Dissertations / Theses on the topic "Metal hydroxides; High resolution"

1

Lakin, Nicholas Mark. "Electronic and microwave spectroscopy of indium(I) hydroxide." Thesis, University of Oxford, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.259963.

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Hodges, Philip J. "Transition metal halides, studied by high-resolution electronic spectroscopy." Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433477.

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Kirkland, Angus Ian. "High resolution electron microscopic studies of colloidal metal particles." Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317850.

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Janczyk, Alexandra Julia. "High Resolution Millimeter-Wave Spectroscopy of Metal Hydrosulfides and Imides." Diss., Tucson, Arizona : University of Arizona, 2005. http://etd.library.arizona.edu/etd/GetFileServlet?file=file:///data1/pdf/etd/azu%5Fetd%5F1349%5F1%5Fm.pdf&type=application/pdf.

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5

McRae, Reagan. "Investigating metal homeostasis in mammalian cells using high resolution imaging techniques." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/41197.

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The primary aim of the work presented in this thesis is to elucidate novel information regarding the uptake, storage, distributions, and functions of both copper and zinc in mammalian cells by predominantly using a combination of the high resolution imaging modalities, synchrotron radiation X-ray fluorescence microscopy (SXRF) and standard fluorescence imaging. Results from studies using cell permeable, metal ion selective fluorescent probes suggested the presence of labile pools of copper and zinc localized within the mitochondria and Golgi apparatus. Furthermore, SXRF imaging of a cell line defective in the copper transporter, Atox1, revealed intriguing differences in the Cu distribution of Atox1-/- cells compared to the corresponding wild-type cells. Finally, spatially well-resolved SXRF elemental maps of single, adherent mouse cells revealed remarkable changes in the distributions of both zinc and copper as the cells progressed through the cell cycle. Taken together, findings suggested major roles for copper and zinc within a native biological setting.

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Shayesteh, Alireza. "High-resolution infrared emission spectroscopy of diatomic and triatomic metal hydrides." Thesis, University of Waterloo, 2006. http://hdl.handle.net/10012/1216.

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Several hydrides of Group 2 and 12 elements were generated in the gas phase using an emission source that combines an electrical discharge with a high temperature furnace, and their high-resolution infrared emission spectra were recorded with a Fourier transform spectrometer. Two classes of molecules were studied: a) diatomic metal hydrides BeH, MgH, CaH, SrH, ZnH and CdH; b) linear triatomic metal hydrides BeH₂, MgH₂, ZnH₂ and HgH₂.

Infrared emission spectra of BeH, MgH, CaH, SrH, ZnH and CdH free radicals contained several vibration-rotation bands in their ²SIGMA⁺ ground electronic state. The new data were combined with all the previous ground state data from diode laser infrared spectra and pure rotation spectra available in the literature. Spectroscopic constants, i. e. , vibrational band origins, rotational, centrifugal distortion, and spin-rotation interaction constants, were determined for each observed vibrational level by least-squares fitting of all the data. In addition, the data from all isotopologues were fitted simultaneously using the empirical Dunham-type energy level expression for ²SIGMA⁺ states, and correction parameters due to the breakdown of the Born-Oppenheimer approximation were determined. The equilibrium internuclear distances (r_e) of ⁹BeH, ²⁴MgH, ⁴⁰CaH, ⁸⁸SrH, ⁶⁴ZnH and ¹¹⁴CdH were determined to be 1. 342424(2), 1. 729721(1), 2. 002360(1), 2. 146057(1), 1. 593478(2) and 1. 760098(3) angstroms, respectively, and the corresponding r^e distances for ⁹BeD, ²⁴MgD, ⁴⁰CaD, ⁸⁸SrD, ⁶⁴ZnD and ¹¹⁴CdD are 1. 341731(2), 1. 729157(1), 2. 001462(1), 2. 145073(1), 1. 593001(2) and 1. 759695(2) angstroms, respectively.

Gaseous BeH², MgH², ZnH² and HgH² molecules were discovered and unambiguously identified by their high-resolution infrared emission spectra. The ν₃ antisymmetric stretching fundamental band and several hot bands in the ν₃ region were rotationally analyzed, and spectroscopic constants were obtained for almost all naturally-occurring isotopologues. The rotational constants of the 000 ground states were used to determine the r₀ internuclear distances. For BeH₂, ZnH₂, ZnD₂, HgH₂ and HgD₂ molecules, the rotational constants of the 000, 100, 01¹0 and 001 levels were used to determine the equilibrium rotational constants (B_e) and the associated equilibrium internuclear distances r_e. The r_e distances of ZnH₂ and ZnD₂ differed by about 0. 01%, and those of HgH₂ and HgD₂ differed by about 0. 005%. These discrepancies were larger than the statistical uncertainties by one order of magnitude, and were attributed to the breakdown of the Born-Oppenheimer approximation.

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7

Thompsen, Jeffrey Matthew. "High-resolution millimeter-wave spectroscopy of 3d-block transition-metal sulfides." Thesis, The University of Arizona, 2001. http://hdl.handle.net/10150/278773.

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The first pure-rotational spectra of two transition-metal sulfides, copper sulfide (CuS) and manganese sulfide (MnS) have been determined. In addition, the millimeter/sub-millimeter spectra of SrS, SrNH₂ and SrND₂ have been determined for the first time. Electronic ground states have been confirmed with experimental evidence. Results indicate that the bonding trends of the transition-metals sulfides are slightly different than their isovalent analogs, the transition-metal oxides. Furthermore, the study of MnS has allowed for experimental testing of current high spin-state quantum theory, by analysing the spectra using third and fourth-order corrections to the effective Hamiltonian. Highly accurate spectroscopic constants and rotational transition frequencies have been determined for all species.

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8

Flory, Michael Aaron. "High Resolution Spectroscopy of Transition Metal-Containing Free Radicals: Investigating High Angular Momentum States." Diss., The University of Arizona, 2007. http://hdl.handle.net/10150/195805.

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Small diatomic and triatomic 3d transition metal species are excellent model systems for understanding metal-ligand interactions important to larger complexes. Because of the unpaired 3d electrons, these radicals often occur in states with high angular momentum (electron spin, orbital, or nuclear spin). Three questions are particularly relevant to studying monosubstituted 3d metal compounds. What are the fundamental geometric, bonding, and electronic properties? How accurately does currentquantum mechanical theory describe the interactions in high spin states? Assuming these molecules may be present in the interstellar medium, what are the precise transition frequencies that can be used for radioastronomy?To answer these questions, pure rotational spectroscopy has been applied to eleven simple molecules containing 3d transition metals. The small radicals were synthesized in the gas phase and examined in situ. Both direct absorption, submillimeter spectroscopy and Fourier transform microwave spectroscopy were used to cover thefrequency range 8-660 GHz. New synthetic techniques, including oven-insulating methods, use of a longitudinal AC discharge, and emphasis on organometallic precursors, were developed to improve reaction yields.Spectra were recorded for four categories of 3d metal compounds: vanadium molecules, cobalt radicals, zinc species, and several monocyanides. Frequently, the data exhibited signs of perturbations either from low-lying excited electronic states, a common feature with 3d electrons, or from avoided crossings of hyperfine levels. The data were analyzed using effective Hamiltonians, and spectroscopic constants have been determined for rotational, fine structure, and hyperfine interactions. The measurements haveprovided transition frequencies as references for astronomical studies; these values are accurate to within 50 kHz for direct measurements and usually within 100 kHz for frequencies calculated from determined molecular constants.Rotational constants have been used to establish precise molecular geometries. Fine structure and hyperfine data provided insight into 3d metal bonding properties (molecular orbital composition and electron distribution) and structure of electronic state manifolds. In some cases, it was necessary to develop new terms for the Hamiltonian expressions to accurately describe the interactions observed in the spectra. These terms include deperturbation parameters and the first complete description of lambda-doubling for Phi states.

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9

Fletcher, David Anthony. "The study of short lived molecules by high resolution spectroscopy." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.256396.

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Dowlatabadi, Ahmad Baghai. "A high speed, high resolution, self-clocked voltage comparator in a standard digital CMOS process." Diss., Georgia Institute of Technology, 1995. http://hdl.handle.net/1853/14794.

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Books on the topic "Metal hydroxides; High resolution"

1

Treichler, Jürg Andreas. Preserving high resolution in deep-submicron CMOS pipelined A/D converters. Konstanz: Hartung-Gorre, 2010.

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1934-, Swanson Lynwood, and Utlaut Mark William 1949-, eds. High resolution focused ion beams: FIB and its applications : the physics of liquid metal ion sources and ion optics and their application to focused ion beam technology. New York: Kluwer Academic/Plenum Publishers, 2003.

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Orloff, Jon. High Resolution Focused Ion Beams: FIB and its Applications: The Physics of Liquid Metal Ion Sources and Ion Optics and Their Application to Focused Ion Beam Technology. Boston, MA: Springer US, 2003.

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Orloff, Jon. High resolution focused ion beams: FIB and its applications ; the physics of liquid metal ion sources and ion optics and their application to focused ion beam technology. New York, NY: Kluwer Academic/Plenum Publishers, 2003.

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Kahtani, Abdullah A. High resolution spectroscopy of metal borohydrides. 1995.

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United States. National Aeronautics and Space Administration., ed. High resolution video monitoring of coating thickness during plasma spraying. [Washington, DC]: National Aeronautics and Space Administration, 1989.

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Structural characterization and gas reactions of small metal particles by high resolution in-situ TEM and TED: Periodic technical report ... for the period, January 1, 1986-December 31, 1986. [Washington, DC: National Aeronautics and Space Administration, 1987.

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United States. National Aeronautics and Space Administration, ed. Structural characterization and gas reactions of small metal particles by high-resolution, in-situ tem and ted: Semi-annual technical report for the period January 1, 1985 to June 30, 1985. Sunnyvale, CA: Eloret Institute, 1985.

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United States. National Aeronautics and Space Administration, ed. Structural characterization and gas reactions of small metal particles by high resolution in-situ TEM and TED: Semi-annual technical report for the period, July 1, 1985 - September 30, 1985, NSDS-grant NCC2-283. [Washington, DC: National Aeronautics and Space Administration, 1985.

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Book chapters on the topic "Metal hydroxides; High resolution"

1

Blanc, J., M. Broyer, J. Chevaleyre, Ph Dugourd, H. Kühling, P. Labastie, M. Ulbricht, J. P. Wolf, and L. Wöste. "High resolution spectroscopy of small metal clusters." In Small Particles and Inorganic Clusters, 7–12. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76178-2_2.

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Lorraine, Peter W., Ralph A. Hewes, and Denis Drolet. "High Resolution Laser Ultrasound Detection of Metal Defects." In Review of Progress in Quantitative Nondestructive Evaluation, 555–62. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4615-5947-4_73.

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Gross, Heinz. "High Resolution Metal Replication of Freeze-Dried Specimens." In Cryotechniques in Biological Electron Microscopy, 205–15. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72815-0_10.

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Jeong, Hyun Jin, Jae Woo Lee, Sug Whan Kim, and A. Ram Kang. "High-Resolution Spectroscopy of 15 Metal-Poor Stars." In Key Engineering Materials, 851–56. Stafa: Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/0-87849-958-x.851.

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Weyland, M., P. J. Thomas, and P. A. Midgley. "Advances in High Resolution Elemental Analysis Using Image-Spectroscopy." In Metal Matrix Composites and Metallic Foams, 163–68. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527606203.ch29.

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Orloff, Jon, Mark Utlaut, and Lynwood Swanson. "Physics of Liquid Metal Ion Sources." In High Resolution Focused Ion Beams: FIB and its Applications, 21–77. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0765-9_3.

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Wu, M. Ch, Ch Truong, and D. W. Goodman. "High-Resolution Electron Energy-Loss Studies of Metal Oxides." In Adsorption on Ordered Surfaces of Ionic Solids and Thin Films, 230–40. Berlin, Heidelberg: Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-78632-7_21.

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Rödel, J. "From Microcharacterization to Macroscopic Property: A Pathway Discussed on Metal/Ceramic Composites." In High-Resolution Imaging and Spectrometry of Materials, 391–418. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-07766-5_9.

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Hosson, J. Th M., H. B. Groen, B. J. Kooi, and W. P. Velinga. "Metal-Ceramic Interfaces Studied with High Resolution Transmission Electron Microscopy." In Impact of Electron and Scanning Probe Microscopy on Materials Research, 135–59. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4451-3_6.

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Ishida, Yoichi, Hideki Ichinose, and Shun-ichiro Tanaka. "High Resolution Electron Microscopy of Silicon Nitride-Metal Bonded Interfaces." In Ceramic Microstructures ’86, 379–86. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1933-7_39.

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Conference papers on the topic "Metal hydroxides; High resolution"

1

Refki, Siham, Shinji Hayashi, Dmitry V. Nesterenko, Zouheir Sekkat, Yasushi Inoue, and Satoshi Kawata. "Metal-insulator-metal structures for high-resolution sensing." In JSAP-OSA Joint Symposia. Washington, D.C.: OSA, 2014. http://dx.doi.org/10.1364/jsap.2014.19p_c3_5.

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Li, D. D., D. H. Zhang, C. C. Yan, Y. K. Wang, and Z. J. Xu. "Metal-dielectric structures for high resolution imaging." In SPIE Photonics Europe, edited by Allan D. Boardman, Nigel P. Johnson, and Richard W. Ziolkowski. SPIE, 2012. http://dx.doi.org/10.1117/12.923033.

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Redd, Randy, Mark A. Spak, John P. Sagan, Octavia P. Lehar, and Ralph R. Dammel. "Lithographic process for high-resolution metal lift-off." In Microlithography '99, edited by Will Conley. SPIE, 1999. http://dx.doi.org/10.1117/12.350188.

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Lu, Lei, Jiapeng Li, Hoi Sing Kwok, and Man Wong. "High-performance and reliable elevated-metal metal-oxide thin-film transistor for high-resolution displays." In 2016 IEEE International Electron Devices Meeting (IEDM). IEEE, 2016. http://dx.doi.org/10.1109/iedm.2016.7838526.

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Xu, Ting, Yi-Kuei Wu, and L. Jay Guo. "Nanostructured metal-insulator-metal resonators for high-resolution color filtering and spectral imaging." In SPIE OPTO, edited by Ali Adibi, Shawn-Yu Lin, and Axel Scherer. SPIE, 2011. http://dx.doi.org/10.1117/12.874363.

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Verdier, Emma, Marc Faucon, and Rainer Kling. "High-resolution intra-volume coloring of metal-doped glass." In ICALEO® 2017: 36th International Congress on Applications of Lasers & Electro-Optics. Laser Institute of America, 2017. http://dx.doi.org/10.2351/1.5138166.

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7

O'Malley, Erin, Andrew McWilliam, and Brian Chaboyer. "High Resolution Spectroscopic Abundance Analysis of Metal-Poor Stars." In SALT Science Conference 2015. Trieste, Italy: Sissa Medialab, 2016. http://dx.doi.org/10.22323/1.250.0054.

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8

Ihara, I. "High resolution measurements in liquid metal by focused ultrasonic wave." In 26th Annual review of progress in quantitative nondestrictive evaluation. AIP, 2000. http://dx.doi.org/10.1063/1.1307887.

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Tanner, John, Sean Ryan, and John E. Norris. "A High Resolution Spectroscopic Study of Eight Metal-Poor Stars." In International Symposium on Nuclear Astrophysics - Nuclei in the Cosmos - IX. Trieste, Italy: Sissa Medialab, 2010. http://dx.doi.org/10.22323/1.028.0209.

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Hussmann, Stephan, Wolfram Kleuver, and Joerg Groeneweller. "High-resolution linear sensor system for sheet metal width measurement." In Industrial Lasers and Inspection (EUROPTO Series), edited by Malgorzata Kujawinska and Wolfgang Osten. SPIE, 1999. http://dx.doi.org/10.1117/12.364274.

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Reports on the topic "Metal hydroxides; High resolution"

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Wang, Lai-Sheng. High resolution photoelectron spectroscopy of metal clusters and high temperature species. Office of Scientific and Technical Information (OSTI), February 1990. http://dx.doi.org/10.2172/6847333.

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2

Shaw, L. L., and S. A. Muelder. High-resolution imaging of hypervelocity metal jets using advanced high-speed photographic techniques. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/119980.

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3

Kellar, S. A. High-resolution structural studies of ultra-thin magnetic, transition metal overlayers and two-dimensional transition metal oxides using synchrotron radiation. Office of Scientific and Technical Information (OSTI), May 1997. http://dx.doi.org/10.2172/335184.

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4

Bartels, Ludwig. Surface Reactions Following Ultra Fast Substrate Excitation: A Path Towards Atomic Scale Resolution of High-temperature Reactions at Metal Surfaces. Fort Belvoir, VA: Defense Technical Information Center, February 2010. http://dx.doi.org/10.21236/ada564034.

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