Analysis of Ageing Precipitation Behavior of an Aluminum Alloy

2014 ◽  
Vol 488-489 ◽  
pp. 243-247
Author(s):  
Hong Xing Liu ◽  
Jian Bo Zhang ◽  
Qi Ming Liang ◽  
Hai Jun Hu
Keyword(s):  
Electrical Conductivity ◽  
Ageing Time ◽  
Precipitation Behavior ◽  
Scanning Calorimetry ◽  
Exothermic Reactions ◽  
Transmission Electron ◽  
Different Temperatures ◽  
One Step ◽  
Electrical Conductivity Change

The characterization of Al-Cu-Mg-Ag alloy with high Cu:Mg in the process of one-step ageing at the different temperatures has been studied by hardness, electrical conductivity test combining with transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The results show that one endothermic and three exothermic reactions are involved in the curve of DSC experiment for a sample quenched from 520°C. Four samples were aged at the different temperatures greater or less than the peak temperatures of the four reactions. Hardness and electrical conductivity change slowly with ageing time at the low temperature and change fast at the high temperature. GP zones at {100} ɑ planes are the main precipitates in the microstructure of the sample aged at 80°C. Ω and θ phases dominant the microstructure of the samples aged at 170°C, 230°C and 280°C. In addition, the size of precipitates increases fast when the sample aged at higher temperatures.

Characterization of Al2(WO4)3 Synthesized by Co-Precipitation Method

2014 ◽  
Vol 798-799 ◽  
pp. 85-89 ◽  
Author(s):  
E.S.G. Junior ◽  
P.M . Jardim
Keyword(s):  
Precipitation Method ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Tem Analysis ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures ◽  
Co Precipitation ◽  
Alpha Alumina

Al2(WO4)3was synthesized by co-precipitation using Na2WO4and Al (NO3)3as precursors. After drying the precipitate, it was calcined at different temperatures between 500°C and 800°C. The crystallization and degradation temperatures of the samples were evaluated by means of Differential Scanning Calorimetry (DSC), Thermogravimetry (TG) and X-Ray Diffraction (XRD). It was observed that the crystallization starts at around 600°C, however Transmission Electron Microscopy (TEM) analysis showed that at this temperature the sample is partially amorphous. The degradation of the material starts at around 1200°C and at 1400°C the tungsten oxide has almost completely evaporated and the material is transformed mainly in alpha-alumina.

One Step Synthesis and Characterization of Zirconia-Graphene Composites

2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Composite ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Xrd Techniques

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.

Characterization of bi-layered magnetic nanoparticles synthesized via two-step surface-initiated ring-opening polymerization

2015 ◽  
Vol 87 (11-12) ◽  
pp. 1085-1097 ◽  
Author(s):  
Li Wang ◽  
Stefan Baudis ◽  
Karl Kratz ◽  
Andreas Lendlein
Keyword(s):  
Magnetic Nanoparticles ◽  
Ring Opening ◽  
Average Molecular Weight ◽  
Polymer Networks ◽  
Gel Permeation Chromatography ◽  
Degree Of Crystallinity ◽  
Scanning Calorimetry ◽  
H Nmr ◽  
Transmission Electron

AbstractA versatile strategy to integrate multiple functions in a polymer based material is the formation of polymer networks with defined nanostructures. Here, we present synthesis and comprehensive characterization of covalently surface functionalized magnetic nanoparticles (MNPs) comprising a bi-layer oligomeric shell, using Sn(Oct)2 as catalyst for a two-step functionalization. These hydroxy-terminated precursors for degradable magneto- and thermo-sensitive polymer networks were prepared via two subsequent surface-initiated ring-opening polymerizations (ROPs) with ω-pentadecalactone and ε-caprolactone. A two-step mass loss obtained in thermogravimetric analysis and two distinct melting transitions around 50 and 85°C observed in differential scanning calorimetry experiments, which are attributed to the melting of OPDL and OCL crystallites, confirmed a successful preparation of the modified MNPs. The oligomeric coating of the nanoparticles could be visualized by transmission electron microscopy. The investigation of degrafted oligomeric coatings by gel permeation chromatography and 1H-NMR spectroscopy showed an increase in number average molecular weight as well as the presence of signals related to both of oligo(ω-pentadecalactone) (OPDL) and oligo(ε-caprolactone) (OCL) after the second ROP. A more detailed analysis of the NMR results revealed that only a few ω-pentadecalactone repeating units are present in the degrafted oligomeric bi-layers, whereby a considerable degree of transesterification could be observed when OPDL was polymerized in the 2nd ROP step. These findings are supported by a low degree of crystallinity for OPDL in the degrafted oligomeric bi-layers obtained in wide angle X-ray scattering experiments. Based on these findings it can be concluded that Sn(Oct)2 was suitable as catalyst for the preparation of nanosized bi-layered coated MNP precursors by a two-step ROP.

Preparation and Characterization of Hybrid Graphene-ZnS Nanoparticles

2010 ◽  
Vol 663-665 ◽  
pp. 894-897
Author(s):  
Hua Huang ◽  
Hai Hu Yu ◽  
Ling De Zhou ◽  
Er Dan Gu ◽  
De Sheng Jiang
Keyword(s):  
Coupling Effect ◽  
Zinc Acetate Dihydrate ◽  
Graphene Sheets ◽  
Acetate Dihydrate ◽  
Zns Nanoparticles ◽  
Transmission Electron ◽  
Infrared Spectrometer ◽  
One Step ◽  
Average Size

Hybrid Graphene-ZnS nanopaticles (G-ZnS NPs) were prepared by using a solvothermal method. A dispersion of graphite oxide (GO) and zinc acetate dihydrate (Zn(CH3COO)2.2H2O) in dimethl sulfoxide (DMSO) reacted at 180 °C for 12 h in a Telfon-lined stainless steel autoclave. In the reaction, DMSO serves as a sulphide source as well as a reducing agent, resulting formation of the hybrid G-ZnS NPs in one-step. Hybrid G-ZnS NPs were characterized by using a powder X-ray diffractometer, a Fourier-transform infrared spectrometer, a transmission electron microscope, a UV-vis spectrophotometer and a fluorescence spectrophotometer, respectively. In the FTIR spectra, the GO related stretching bands of C-O and carboxyl groups are not observed in the spectra of G-ZnS, suggesting that the GO sheets were reduced to graphene sheets. In the TEM images, it is observed that the ZnS nanoparticles with an average size of 23 nm are attached onto the graphene sheets. The UV-vis absorption spectrum of the G-ZnS NPs dispersed in ethanol has an absorption peak of G at 261 nm and a weak shoulder of ZnS NPs around 320 nm. The broadening and weakening of the peak of ZnS NPs at 320 nm arises from the interparticle coupling effect. Under excitation at 225 nm, a peak around 386 nm and other weaker bands appear in the fluorescence spectrum of the G-ZnS. The band at 386 nm is attributed to zinc vacancies.

Preparation and Property of Al87Ce3Ni8.5Mn1.5 Nanophase Amorphous Composites

2011 ◽  
Vol 412 ◽  
pp. 263-266
Author(s):  
Hong Wei Zhang ◽  
Li Li Zhang ◽  
Feng Rui Zhai ◽  
Jia Jin Tian ◽  
Can Bang Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Phase ◽  
Volume Fraction ◽  
Material Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures

The higher mechanical strength of Al87Ce3Ni8.5Mn1.5 nanophase amorphous composites has been obtained with two methods. The first nanophase amorphous composites are directly produced by the single roller spin quenching technology. The method taken for the second nanophase amorphous composites is at first to obtain amorphous single-phase alloy, followed by annealed at different temperatures .The formative condition, the microstructure, the particle size, the volume fraction of α-Al phase and microhardness of nanophase amorphous composites etc have been investigated and compared by X-ray diffraction (XRD) and transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The microstructure of composites produced by the second method is higher than the former, the fabricated material structure of the system is more uniform and the process is easier to control.

Growth and Characterization of Cobalt-filled Carbon Nanotubes Prepared by a Simple Catalytic Method

2003 ◽  
Vol 776 ◽  
Author(s):  
Xicheng Ma ◽  
Yuanhua Cai ◽  
Xia Li ◽  
Ning Lun ◽  
Shulin Wen
Keyword(s):  
Carbon Nanotubes ◽  
Metallic Nanoparticles ◽  
Low Cost ◽  
Catalytic Method ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
High Resolution Tem ◽  
One Step

AbstractHigh-quality cobalt-filled carbon nanotubes (CNTs) were prepared in situ in the decomposition of benzene over Co/silica-gel nano-scale catalysts. Unlike the previous reports, the catalysts needn't be pre-reduced prior to the forming of Co-filled CNTs, thus the advantage of this method is that Co-filled CNTs can be produced in one step, at a relatively low cost. Transmission electron microscopy (TEM) investigation showed that the products contained abundance of CNTs and most of them were filled with metallic nanoparticles or nanorods. High-resolution TEM (HRTEM), selected area electron diffraction (SAED) patterns and energy dispersive X-ray spectroscopy (EDS) confirmed the presence of Co inside the nanotubes. The encapsulated Co was further identified always as high temperature alpha-Co phase with fcc structure, which frequently consists of twinned boundaries and stacking faults. Based on the experimental results, a possible growth mechanism of the Co-filled CNTs was proposed.

scholarly journals Hydrothermal Synthesis and Characterization of Single-Crystalline -Fe2O3Nanocubes

2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Wenqing Qin ◽  
Congren Yang ◽  
Ran Yi ◽  
Guanhua Gao
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Infrared Spectrometry ◽  
X Ray Diffraction ◽  
Single Crystalline ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Alkaline Agent ◽  
One Step

Single-crystalline - nanocubes were successfully obtained in large quantities through a facile one-step hydrothermal synthetic route under mild conditions. In this synthetic system, aqueous iron (III) nitrate () served as iron source and triethylamine served as precipitant and alkaline agent. By prolonging reaction time from 1 h to 24 h, the evolution process of -, from nanorhombohedra to nanohexahedron, and finally nanocube, was observed. The products were characterized by Powder X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), High-resolution Transmission Electron Microscopy (HRTEM), Selected-Area Electron Diffraction (SAED), and Fourier Transform Infrared Spectrometry (FTIR). The possible formation mechanism was discussed on basis of the experimental results.

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