Characterization and Modeling of Precipitation Kinetics in Aluminium 7000 Alloys

1999 ◽  
Vol 578 ◽  
Author(s):  
J.C. Werenskiold ◽  
A. Deschamps
Keyword(s):  
Internal State ◽  
Isothermal Heat Treatment ◽  
Precipitation Kinetics ◽  
Variable Model ◽  
Microstructural Parameters ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Wide Range ◽  
Modeling And Experiments

AbstractThe precipitation kinetics of 7108.70 aluminum alloy has been investigated in a wide range of temperatures by in situ Small Angle X-ray Scattering (SAXS) and Transmission Electron Microscopy (TEM), and computer modeled by use of an internal-state variable model which predicts the evolution of microstructural parameters. The modeling and experiments were done for isothermal heat treatment at 120, 140, 150, 160 and 170°C. The industrial T6 and T7 treatments have also been investigated.

On the selective aerobic oxidation of benzyl alcohol with Pd/Au-nanoparticles in batch and flow

2014 ◽  
Vol 3 (1) ◽  
pp. 99-110 ◽  
Author(s):  
Hannes Alex ◽  
Norbert Steinfeldt ◽  
Klaus Jähnisch ◽  
Matthias Bauer ◽  
Sandra Hübner
Keyword(s):  
Catalytic Activity ◽  
Benzyl Alcohol ◽  
Aerobic Oxidation ◽  
X Ray ◽  
X Ray Scattering ◽  
Oxidation Of Benzyl Alcohol ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
Selective Aerobic Oxidation

AbstractNanoparticles (NP) have specific catalytic properties, which are influenced by parameters like their size, shape, or composition. Bimetallic NPs, composed of two metal elements can show an improved catalytic activity compared to the monometallic NPs. We, herein, report on the selective aerobic oxidation of benzyl alcohol catalyzed by unsupported Pd/Au and Pd NPs at atmospheric pressure. NPs of varying compositions were synthesized and characterized by UV/Vis spectroscopy, transmission electron microscopy (TEM), and small-angle X-ray scattering (SAXS). The NPs were tested in the model reaction regarding their catalytic activity, stability, and recyclability in batch and continuous procedure. Additionally, in situ extended X-ray absorption fine structure (EXAFS) measurements were performed in order to get insight in the process during NP catalysis.

scholarly journals Sample Preparation Methodologies for In Situ Liquid and Gaseous Cell Analytical Transmission Electron Microscopy of Electropolished Specimens

2016 ◽  
Vol 22 (6) ◽  
pp. 1350-1359 ◽  
Author(s):  
Xiang Li Zhong ◽  
Sibylle Schilling ◽  
Nestor J. Zaluzec ◽  
M. Grace Burke
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Focused Ion Beam ◽  
General Procedure ◽  
Ion Beam ◽  
Metals And Alloys ◽  
Stainless Steel Sample ◽  
Transmission Electron ◽  
Wide Range

AbstractIn recent years, an increasing number of studies utilizing in situ liquid and/or gaseous cell scanning/transmission electron microscopy (S/TEM) have been reported. Because of the difficulty in the preparation of suitable specimens, these environmental S/TEM studies have been generally limited to studies of nanoscale structured materials such as nanoparticles, nanowires, or sputtered thin films. In this paper, we present two methodologies which have been developed to facilitate the preparation of electron-transparent samples from conventional bulk metals and alloys for in situ liquid/gaseous cell S/TEM experiments. These methods take advantage of combining sequential electrochemical jet polishing followed by focused ion beam extraction techniques to create large electron-transparent areas for site-specific observation. As an example, we illustrate the application of this methodology for the preparation of in situ specimens from a cold-rolled Type 304 austenitic stainless steel sample, which was subsequently examined in both 1 atm of air as well as fully immersed in a H2O environment in the S/TEM followed by hyperspectral imaging. These preparation techniques can be successfully applied as a general procedure for a wide range of metals and alloys, and are suitable for a variety of in situ analytical S/TEM studies in both aqueous and gaseous environments.

“In-Situ Network” Composite Fibers of Pbzt/Nylon

1988 ◽  
Vol 134 ◽  
Author(s):  
C. Robin Hwang ◽  
Michael F. Malone ◽  
Richard J. Farris ◽  
David C. Martin ◽  
Edwin L. Thomas
Keyword(s):  
Nitrogen Adsorption ◽  
Composite Fibers ◽  
Electron Microscopies ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Before And After ◽  
The Matrix ◽  
Novel Method ◽  
20 Nm

ABSTRACTA novel method of preparing PBZT/nylon composite fibers by infiltrating nylon into pure PBZT fiber is described. The pure PBZT fiber formed a microfibrillar network structure during coagulation, which is effective in reinforcing the matrix in the “in-situ network” composite fibers (designated IC). These new composite fibers exhibit nearly indistinguishable mechanical properties as those of “molecular” composite fibers (MC) prepared from isotropic solutions before and after tension heat-treatment (E = 44 GPa, σ = 430 MPa, ε = 1.2 %, σc = 250 MPa, G = 1.75 GPa) for PBZT/nylon weight ratios equal to unity.The fine structure of pure PBZT and its composite fibers spun from isotropic solutions was characterized using techniques based on nitrogen adsorption, small-angle X-ray scattering, scanning and transmission electron microscopies. The structure of both type of composites was found to be a microfibrillar network of PBZT in a matrix of amorphous nylon. The average diameters of the PBZT microfibrils were in the range of 10 to 20 nm for the IC and 4 nm for the MC.

Development of Wet Environmental TEM (Wet-ETEM) for In Situ Studies of Liquid-Catalyst Reactions on the Nanoscale

2002 ◽  
Vol 8 (1) ◽  
pp. 21-28 ◽  
Author(s):  
Pratibha L. Gai
Keyword(s):  
Biological Sciences ◽  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
High Resolution ◽  
Transmission Electron ◽  
Wide Range ◽  
Environmental Tem ◽  
Nanoscale Imaging ◽  
Solution Gas

We present the development of in situ wet environmental transmission electron microscopy (Wet-ETEM) for direct probing of controlled liquid–catalyst reactions at operating temperatures on the nanoscale. The first nanoscale imaging and electron diffraction of dynamic liquid hydrogenation and polymerization reactions in the manufacture of polyamides reported here opens up new opportunities for high resolution studies of a wide range of solution–solid and solution–gas–solid reactions in the chemical and biological sciences.

The Influence of Mg and Ag on the Precipitation Kinetics and the Formation of the T1 Phase in Al-Cu-Li Alloys

2014 ◽  
Vol 794-796 ◽  
pp. 945-950 ◽  
Author(s):  
Eva Gumbmann ◽  
Frederic de Geuser ◽  
Williams Lefebvre ◽  
Christophe Sigli ◽  
Alexis Deschamps
Keyword(s):  
Cold Deformation ◽  
Precipitation Kinetics ◽  
Nucleation Kinetics ◽  
Aerospace Applications ◽  
X Ray Scattering ◽  
Common Content ◽  
Precipitate Nucleation ◽  
The Impact ◽  
Kinetics Of

Al-Cu-Li alloys are extensively used for aerospace applications. The main hardening phase is the T1phase that precipitates as thin platelets on {111}Alplanes. To facilitate its nucleation, different minor alloying elements are added and dislocations are introduced by cold deformation before the ageing treatment. The impact of these additions in combination with the presence of dislocations on precipitate nucleation and growth needs a deeper understanding. In this work, we investigated the precipitation kinetics of the T1phase in alloys containing a common content of Cu and Li and different contents of minor solutes (Mg, Ag) where these elements are present either together or independently. A general overview on the precipitation kinetics was achieved by in-situ small-angle X-ray scattering and hardness measurements. The evaluation of precipitation kinetics reveals that magnesium plays an important role during precipitation by enhancing nucleation kinetics. Additionally, a smaller yet measureable effect of Ag, both in the presence and absence of Mg has been evidenced.

Stratified Ion Damage and in Situ Regrowth in GaAs/AlAs Heterostructures

1990 ◽  
Vol 201 ◽  
Author(s):  
A G Cullis ◽  
D J Eaglesham ◽  
D C Jacobson ◽  
J M Poate ◽  
C R Whitehouse ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Point Defects ◽  
Multilayer Structures ◽  
Dependent Manner ◽  
Characteristic Boundary ◽  
Transmission Electron ◽  
Wide Range ◽  
Ion Damage ◽  
Lattice Damage

AbstractThe material-dependent manner in which ion damage occurs in AlAs/GaAs heteroepitaxial structures is demonstrated using conventional and high resolution transmission electron microscopy. Both 150keV and 2MeV Si+ ion implants are employed over a wide range of ion doses. Under conditions which yield rapid build-up of lattice damage in GaAs, the AlAs is found to be relatively resistant to structure breakdown. Indeed, the crystalline AlAs exerts a novel protective effect on immediately adjacent regions of the GaAs layers. For high implantation doses amorphous-crystal superlattices are formed in multilayer structures. For the highest ion doses the AlAs lattice begins to be disrupted by a characteristic, boundary-dependent, heterogeneous mechanism. These observations suggest that mobile point defects play a significant role in AlAs in situ restructuring processes.

scholarly journals In Situ and In Operando Techniques to Study Li-Ion and Solid-State Batteries: Micro to Atomic Level

Inorganics ◽  
2021 ◽  
Vol 9 (11) ◽  
pp. 85
Author(s):  
Maryam Golozar ◽  
Raynald Gauvin ◽  
Karim Zaghib
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Atomic Level ◽  
X Ray ◽  
In Situ Techniques ◽  
Transmission Electron ◽  
Wide Range ◽  
Li Ion

This work summarizes the most commonly used in situ techniques for the study of Li-ion batteries from the micro to the atomic level. In situ analysis has attracted a great deal of interest owing to its ability to provide a wide range of information about the cycling behavior of batteries from the beginning until the end of cycling. The in situ techniques that are covered are: X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), and Scanning Transmission Electron Microscopy (STEM). An optimized setup is required to be able to use any of these in situ techniques in battery applications. Depending on the type of data required, the available setup, and the type of battery, more than one of these techniques might be needed. This study organizes these techniques from the micro to the atomic level, and shows the types of data that can be obtained using these techniques, their advantages and their challenges, and possible strategies for overcoming these challenges.

Application of in situ Transmission Electron Microscopyfor Tribological Investigations of Magnetron Sputter Assisted Pulsed Laser Deposition of Yttria-stabilized Zirconia-gold Composite Coatings

2005 ◽  
Vol 20 (7) ◽  
pp. 1860-1868 ◽  
Author(s):  
J.J. Hu ◽  
A.A. Voevodin ◽  
J.S. Zabinski
Keyword(s):  
Electron Microscopy ◽  
High Temperature ◽  
Composite Coatings ◽  
Pulsed Laser ◽  
Yttria Stabilized Zirconia ◽  
Stabilized Zirconia ◽  
X Ray ◽  
Transmission Electron ◽  
Wide Range

Yttria-stabilized zirconia (YSZ)-Au composite coatings have great potential as solid film lubricants for aerospace applications over a wide range of environmental conditions. They were grown on steel disks or silicon wafers by pulsed laser ablation of YSZ and simultaneous magnetron sputtering of a Au target. Such a combination of ceramics with soft metals improved the toughness of the composite coating and increased its ability to lubricate at high temperature. Information on the time-dependent response of these microstructures to changes in temperature is essential to tribological investigations of high temperature performance. In situ transmission electron microscopy was used to directly measure the dynamic change of YSZ-Au coating structure at elevated temperatures. High-resolution electron microscopy and electron diffraction showed that amorphous YSZ-5 at.% Au coatings proceeded to crystallize under the irradiation of electron beams. Time varying x-ray energy dispersive spectra measured a loss of oxygen in the sample during about 10 min of irradiation with subsequent slight oxygen recovery. This behavior was related to the activation of oxygen diffusion under electron irradiation. X-ray diffraction patterns from vacuum annealed samples verified crystallization of the coatings at 500 °C. Real-time growth of Au nanograins in the sample was observed as the temperature was increased to 500 °C in a TEM specimen holder that could be heated. The grain growth process was recorded using a charge-coupled device camera installed on the transmission electron microscope. The crystallization and growth of zirconia and Au nanograins resulted in low friction during tribological tests. The nucleation of Au islands on heated ball-on-flat specimens was responsible for lowering friction.

scholarly journals In Situ Nitroxide-Mediated Polymerized Poly(acrylic acid) as a Stabilizer/Compatibilizer Carbon Nanotube/Polymer Composites

2007 ◽  
Vol 2007 ◽  
pp. 1-12 ◽  
Author(s):  
Vitaliy Datsyuk ◽  
Laurent Billon ◽  
Christelle Guerret-Piécourt ◽  
Sylvie Dagréou ◽  
Nicolas Passade-Boupatt ◽  
...  
Keyword(s):  
Carbon Nanotube ◽  
Acrylic Acid ◽  
Polymer Composites ◽  
Diblock Copolymers ◽  
Polymer Network ◽  
Electron Microscopies ◽  
Transmission Electron ◽  
Wide Range ◽  
Poly Acrylic Acid

Carbon nanotube (CNT) polymer composites were synthesized via in situ nitroxide-mediated diblock copolymerization. Poly(acrylic acid) (PAA) was chosen as a first block to obtain a precomposite CNT-PAA which is readily dispersible in various solvents including water. The immobilization of the stable poly(acrylic acid) alkoxyamine functionality on the nanotube surface occurs during the synthesis of the first block without CNT prior treatment. The living character of this block is established by spectroscopic methods and the nature of the CNT/PAA interaction is discussed. This living first block offers the opportunity to reinitiate the polymerization of a second block that can be chosen among a wide range of monomers. This versatility is illustrated with a second block containing methyl acrylate (MA) or styrene (S). Scanning and transmission electron microscopies confirm good CNT dispersion in the polymer network, while transmission electron microscopy also spots the anchorage locations of PAA on the CNT surface. Such nanotubes wrapped by diblock copolymers can be dispersed in various polymer matrices to create CNT—polymer composites. Conductivity measurements show that these composites obey a percolation-like power law with a low percolation threshold (less than 0.5 vol%) and a high maximum conductivity (up to 1.5 S/cm at room temperature).

Experimental setup forin situX-ray SAXS/WAXS/PDF studies of the formation and growth of nanoparticles in near- and supercritical fluids

2010 ◽  
Vol 43 (4) ◽  
pp. 729-736 ◽  
Author(s):  
Jacob Becker ◽  
Martin Bremholm ◽  
Christoffer Tyrsted ◽  
Brian Pauw ◽  
Kirsten Marie Ø. Jensen ◽  
...  
Keyword(s):  
Supercritical Fluids ◽  
Inorganic Nanoparticles ◽  
Great Promise ◽  
Synthesis Methods ◽  
Experimental Setup ◽  
X Ray ◽  
X Ray Scattering ◽  
Wide Range ◽  
Ray Scattering

The growing interest in inorganic nanoparticles for a wide range of applications is spurring a need for synthesis methods that allow a highly specific tailoring of material properties. Synthesis in supercritical fluids holds great promise for solving this problem, but so far the fundamental chemical processes taking place under these conditions are to a large extent unknown. Here the design, construction and application of a versatile experimental setup are reported; this setup enablesin situsynchrotron small-angle X-ray scattering/wide-angle X-ray scattering/pair distribution function (SAXS/WAXS/PDF) studies of the formation and growth of nanoparticles under supercritical fluid conditions.

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