“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.

Blends containing core-shell impact modifiers Part 1. Structure and tensile deformation mechanisms (IUPAC Technical Report)

2001 ◽  
Vol 73 (6) ◽  
pp. 897-912 ◽  
Author(s):  
C. B. Bucknall
Keyword(s):  
Tensile Deformation ◽  
Tensile Tests ◽  
Mechanical Tests ◽  
Glass Transitions ◽  
Volume Increase ◽  
Transmission Electron ◽  
Technical Report ◽  
The Matrix ◽  
20 Nm

Two impact modifiers, based respectively on polybutadiene (PB) and poly(butyl acrylate-co-styrene) (PBA), are compared in blends with four glassy polymers: polycarbonate (PC), poly(methyl methacrylate) (PMMA), poly(styrene-co-acrylonitrile) (PSAN), and poly(vinyl chloride) (PVC). Dynamic mechanical tests show glass transitions at about -80 °C in PB and -15 °C in PBA. Both modifiers have grafted PMMA shells, which are seen in the transmission electron microscope (TEM) to be about 10 nm thick. The two-stage PB particles have 200-nm-diameter polybutadiene cores, whereas the three-stage PBA particles have 260-nm-diameter PMMA cores, with 20-nm thick PBA rubber inner shells. Under tension, the PB particles cavitate to form single voids on reaching a critical volume strain, and subsequently offer little resistance to dilatation. By contrast, tensile tests performed in situ in the TEM show that the PBA shells form fibrils that are anchored to the rigid core, and act as constraints on further dilatation: the stresses developed in the PBA fibrils can be sufficient to draw fibrils from both the PMMA core and the PSAN matrix. There is evidence that the PMMA shells can debond from the matrix both in cryogenic fracture and in fatigue at 23 °C. Tensile dilatometry shows that the PB particles cavitate at higher strains than the PBA particles, but that the PB particles then cause a rapid volume increase, leading to a low strain at break. By contrast, the PBA particles produce a more controlled dilatation, and higher strains to break. Later papers in this series treat the mechanical and rheological behavior of these blends in more detail.

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 Nanocomposites of Polyaniline and Cellulose Nanocrystals Prepared in Lyotropic Chiral Nematic Liquid Crystals

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Dawei Zhang ◽  
Lihong Zhang ◽  
Bingzhe Wang ◽  
Guangzhe Piao
Keyword(s):  
Liquid Crystals ◽  
Cellulose Nanocrystals ◽  
Nematic Liquid Crystals ◽  
Weight Ratio ◽  
Asymmetric Reaction ◽  
Reaction Field ◽  
Electron Microscopies ◽  
Chiral Nematic ◽  
Before And After

Stable lyotropic chiral nematic liquid crystals (N*-LCs) of cellulose nanocrystals (CNs) were prepared via hydrolysis using sulfuric acid. The lyotropic N*-LCs were used as an asymmetric reaction field to synthesize polyaniline (PANI) onto CNs by in situ polymerization. As a primary step, we examined the mesophase transition of the N*-LCs of CNs suspension before and after in situ polymerization of aniline (ANI) by polarizing optical microscopy. The structure of nanocomposites of PANI/CNs was investigated at a microscopic level using Fourier transform infrared spectroscopy and X-ray diffraction. Influence of the CNs-to-ANI ratio on the morphology of the nanocomposites was also investigated at macroscopic level by scanning electron and transmission electron microscopies. It is found that the weight ratio of CNs to aniline in the suspension significantly influenced the size of the PANI particles and interaction between CNs and PANI. Moreover, electrical properties of the obtained PANI/CNs films were studied using standard four-probe technique. It is expected that the lyotropic N*-LCs of CNs might be available for an asymmetric reaction field to produce novel composites of conjugated materials.

scholarly journals High-Resolution Microstructure Characterization of Additively Manufactured X5CrNiCuNb17-4 Maraging Steel during Ex and in Situ Thermal Treatment

2021 ◽  
Author(s):  
Mihaela Albu ◽  
Bernd Panzirsch ◽  
Hartmuth Schröttner ◽  
Stefan Mitsche ◽  
Klaus Reichmann ◽  
...  
Keyword(s):  
Maraging Steel ◽  
Elevated Temperatures ◽  
Scanning Transmission Electron Microscope ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
The Matrix ◽  
Powder Particles ◽  
In Situ Heating ◽  
Heating Up

Powder and SLM additively manufactured parts of X5CrNiCuNb17-4 maraging steel were systematically investigated by electron microscopy to understand the relationship between the properties of the powder grains and the microstructure of the printed parts. We prove that satellites, irregularities and superficial oxidation of powder particles can be transformed into an advantage through the formation of nanoscale (AlMnSiTiCr)-oxides in the matrix during the printing process. The nano-oxides showed extensive stability in terms of size, spherical morphology, chemical composition and crystallographic disorder upon in situ heating up to 950°C in the scanning transmission electron microscope. Their presence thus indicates a potential for oxide-dispersive strengthening of this steel, which may be beneficial for creep resistance at elevated temperatures. The nucleation of copper clusters and their evolution into nanoparticles as well as the precipitation of Ni and Cr particles upon in situ heating have as well been systematically documented.

Influence of ethanol on the chain-ordering of carbonised polyaniline

2013 ◽  
Vol 67 (8) ◽  
Author(s):  
Zuzana Morávková ◽  
Miroslava Trchová ◽  
Elena Tomšík ◽  
Jaroslav Stejskal
Keyword(s):  
Molecular Structure ◽  
Pure Water ◽  
Nitrogen Atmosphere ◽  
Ethanol Mixture ◽  
Electron Microscopies ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Pani Salt ◽  
Chain Ordering ◽  
Pani Base

AbstractPolyaniline (PANI) was prepared by the oxidation of aniline hydrochloride with ammonium peroxydisulphate in water or in a water-ethanol mixture. In the presence of ethanol, PANI nanotubes and nanorods were observed. Both products were carbonised in a nitrogen atmosphere at 650°C. Initial and carbonised products were characterised by scanning and transmission electron microscopies, thermogravimetric analysis and wide-angle X-ray scattering. Their molecular structure was studied by UV-VIS, infrared, and Raman spectroscopies. Carbonised sample obtained from the PANI salt prepared in the presence of ethanol exhibits Raman spectrum which corresponds to a more ordered carbon-like material than carbonised samples obtained from the PANI base and the PANI salt prepared in pure water. The influence of ethanol present in the reaction mixture on the molecular and supra-molecular structure of PANI and, consequently, on the enhancement of chainordering of carbonised PANI is discussed.

Microstructural Characterization, Mechanical Properties and Wear Resistance of TiCP Reinforced Ni-Alloy Coatings by Laser Synthesis

2000 ◽  
Author(s):  
D. L. Tu ◽  
A. Kar ◽  
X. L. Wu
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Wear Resistance ◽  
Chemical Reaction ◽  
Phase Interface ◽  
High Fracture Toughness ◽  
Transmission Electron ◽  
Ni Alloy ◽  
The Matrix

Abstract Titanium carbide particle (TiCp)-reinforced Ni alloy composite coatings are synthesized by laser cladding using a cw 3 kW CO2 laser. Two kinds of coatings are possible in terms of the origin of TiCp: undissolved TiCp and in-situ generated TiCp. The former originates from the TiCp pre-coated on the sample whereas the latter from in-situ chemical reaction between titanium and graphite in the molten pool during laser irradiation. For the coating reinforced by TiCp formed in-situ, the sub-micron TiCp particles are formed and uniformly distributed because of the in-situ reaction and trapping effect during rapid solidification. Graded distribution of TiCp is obtained on a macro scale. The volume fraction increases from 1.86% at the coating-substrate interface to 38.4% at the coating surface. For the coating reinforced by undissolved TiCp, analytical transmission electron microscopy (ATEM) and high resolution transmission electron microscopy (HRTEM) observations show the existence of the epitaxial growth of TiC, the precipitation of CrB and M23C6, and the chemical reaction between Ti and B elements around phase interfaces of undissolved TiCp. In the matrix near the phase interface of undissolved TiCp, the loading curve obtained by nanoindenter exhibits pop-in phenomena due to the plastic deformation of cracks or debonding of TiCp from the matrix. For TiCp generated in-situ, no pop-in mark appears, indicating high fracture toughness. Coating with TiCp generated in-situ exhibits higher hardness and modulus than the coating with undissolved TiCp at regions near the phase interface. The coating reinforced by TiCp generated in-situ also displays higher impact wear resistance and abrasive wear resistance compared to the coatings with undissolved TiCp and without TiCp respectively.

Direct Preparation of Ce0.8Sm0.2O1.9 Powders Oxidized With H2O2 for Low Temperature SOFCs Application

2005 ◽  
Author(s):  
Jianbing Huang ◽  
Zongqiang Mao ◽  
Bin Zhu ◽  
Lizhai Yang ◽  
Ranran Peng ◽  
...  
Keyword(s):  
Single Phase ◽  
Fluorite Structure ◽  
X Ray Diffraction ◽  
Composite Electrolyte ◽  
Xrd Pattern ◽  
Transmission Electron ◽  
Direct Preparation ◽  
Novel Method ◽  
Power Densities

A novel method was developed to prepare fine doped ceria (DCO) powders directly. Ceria doped with 20 mol. % of samarium (Ce0.8Sm0.2O1.9, SDC) was prepared by in-situ oxidization of hydroxide precipitates with H2O2 in the solutions. The resultant powder desiccated at 85°C overnight was characterized by X-ray diffraction (XRD), thermogravimetry /differential thermal analysis (TG/DTA), and transmission electron microscopy (TEM). The XRD pattern showed that the as-dried SDC powder is single phase with a cubic fluorite structure like that of pure CeO2. An anode-supported SOFC was also fabricated based on SDC and 20wt. % (62mol. %Li2CO3–38 mol. %K2CO3) composite electrolyte, LiNiO2 as cathode and NiO as anode, by cold pressing. Using hydrogen as the fuel and air as the oxidant, the I-V and I-P characteristics exhibit excellent performances and the maximum power densities are about 696, 469, 377 and 240 mWcm−2 at 650, 600, 550 and 500°C, respectively.

scholarly journals Anti-twinning in nanoscale tungsten

2020 ◽  
Vol 6 (23) ◽  
pp. eaay2792
Author(s):  
Jiangwei Wang ◽  
Zhi Zeng ◽  
Minru Wen ◽  
Qiannan Wang ◽  
Dengke Chen ◽  
...  
Keyword(s):  
Nucleation And Growth ◽  
Shear Displacement ◽  
Atomic Scale ◽  
Deformation Mechanisms ◽  
Body Centered Cubic ◽  
Plastic Shear ◽  
Transmission Electron ◽  
20 Nm ◽  
Scale Shear

Nanomaterials often surprise us with unexpected phenomena. Here, we report a discovery of the anti-twinning deformation, previously thought impossible, in nanoscale body-centered cubic (BCC) tungsten crystals. By conducting in situ transmission electron microscopy nanomechanical testing, we observed the nucleation and growth of anti-twins in tungsten nanowires with diameters less than about 20 nm. During anti-twinning, a shear displacement of 1/3〈111〉 occurs on every successive {112} plane, in contrast to an opposite shear displacement of 1/6〈1¯1¯1¯〉 by ordinary twinning. This asymmetry in the atomic-scale shear pathway leads to a much higher resistance to anti-twinning than ordinary twinning. However, anti-twinning can become active in nanosized BCC crystals under ultrahigh stresses, due to the limited number of plastic shear carriers in small crystal volumes. Our finding of the anti-twinning phenomenon has implications for harnessing unconventional deformation mechanisms to achieve high mechanical preformation by nanomaterials.

scholarly journals Study of the Microstructure and Crack Evolution Behavior of Al-5Fe-1.5Er Alloy

Materials ◽  
2019 ◽  
Vol 12 (1) ◽  
pp. 172 ◽  
Author(s):  
Ming Li ◽  
Zhiming Shi ◽  
Xiufeng Wu ◽  
Huhe Wang ◽  
Yubao Liu
Keyword(s):  
Electron Microscopy ◽  
Crack Initiation ◽  
Tensile Tests ◽  
Eutectic Structure ◽  
Interface Structure ◽  
X Ray ◽  
Transmission Electron ◽  
The Matrix ◽  
Evolution Behavior

In this work, the microstructure of Al-5Fe-1.5Er alloy was characterized and analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy-dispersive X-ray spectroscopy (EDS) techniques. The effect of microstructure on the behavior of crack initiation and propagation was investigated using in situ tensile testing. The results showed that when 1.5 wt.% Er was added in the Al-5Fe alloy, the microstructure consisted of α-Al matrix, Al3Fe, Al4Er, and Al3Fe + Al4Er eutectic phases. The twin structure of Al3Fe phase was observed, and the twin plane was {001}. Moreover, a continuous concave and convex interface structure of Al4Er was observed. Furthermore, Al3Fe was in the form of a sheet with a clear gap inside. In situ tensile tests of the alloy at room temperature showed that the crack initiation mainly occurred in the Al3Fe phase, and that the crack propagation modes included intergranular and trans-granular expansions. The crack trans-granular expansion was due to the strong binding between Al4Er phases and surrounding organization, whereas the continuous concave and convex interface structure of Al4Er provided a significant meshing effect on the matrix and the eutectic structure.

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