Determination of phase relations in the Co–Cu–Ti system by the diffusion triple technique

2006 ◽  
Vol 21 (10) ◽  
pp. 2493-2503 ◽  
Author(s):  
H.S. Liu ◽  
Y.M. Wang ◽  
L.G. Zhang ◽  
Q. Chen ◽  
F. Zheng ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Electron Probe ◽  
Composition Range ◽  
Invariant Reaction ◽  
Isothermal Sections ◽  
The Third ◽  
Diffusion Triple ◽  
Binary Compounds ◽  
Scanning Electron

Two isothermal sections of the Co–Cu–Ti ternary system at 973 and 1123 K were experimentally determined using the diffusion triple technique together with scanning electron microscopy and electron probe microanalysis. The solubility of Cu (substituting Co) in CoTi increased from 22.8 at.% at 973 K to 28.1 at.% at 1123 K while that of Co (substituting Cu) in CuTi decreased from 11.1 to 8.8 at.% accordingly. In addition, the solubility limits of the third element in the binary compounds CoTi2, CuTi2, Cu4Ti3, and Cu3Ti2 were remarkable. Besides the solubility change, we found the Cu2Ti phase was stable at 1123 K but disappeared at 973 K. A ternary compound “m” with a composition range covering Co10Cu57Ti33 was detected at both isothermal sections. An invariant reaction Cu4Ti3 + CoTi ↔ CuTi + m at a temperature between 973 and 1023 K was deduced. Further investigations are necessary to confirm the reactions among Cu, Cu4Ti, Cu2Ti, Cu3Ti2, and “m” between 1023 and 1123 K.

scholarly journals Phase equilibria of the Al-Co-Er system at 400°C and 600°C

2021 ◽  
pp. 32-32
Author(s):  
L.-H. Zheng ◽  
L.-G. Zhang ◽  
F.-Y. Zhao ◽  
L.-B. Liu ◽  
D. Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Isothermal Section ◽  
Electron Probe ◽  
X Ray Diffraction ◽  
Isothermal Sections ◽  
X Ray ◽  
Solid Solution Range ◽  
Three Phase ◽  
Phase Fields ◽  
Scanning Electron

The 400?C and 600?C isothermal sections of the Al-Co-Er system were studied assisted with X-ray diffraction (XRD), scanning electron microscopy (SEM) and electron probe microanalysis (EPMA) techniques. 18 three-phase fields were identified in the 400?C isothermal section. The maximum solid solubilities of Al in Co3Er and Co2Er were 13.93 at.% and 16.13 at.%, respectively. Whereas the maximum solid solubilities of Co in Al2Er, Al2Er3 and AlEr2 were 6.93 at.%, 6.65 at.%, and 6.49 at.%, respectively. And the solid solution range of ? is from 22.22 at.% Al to 44.44 at.% Al. While the 600?C isothermal section included 20 three-phase fields. The maximum solid solubilities of Al in Co17Er2 and Co7Er2 were 10.17 at.% and 10.24 at.%, respectively. Whereas the maximum solid solubilities of Co in Al2Er and Al2Er3 were 3.63 at.% and 2.01 at.%, respectively.

scholarly journals Influence of microstructure on symmetry determination of piezoceramics

2018 ◽  
Vol 51 (3) ◽  
pp. 670-678 ◽  
Author(s):  
M. Hinterstein ◽  
H. E. Mgbemere ◽  
M. Hoelzel ◽  
W. Rheinheimer ◽  
E. Adabifiroozjaei ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Diffraction Data ◽  
Electron Probe Microanalysis ◽  
Electron Probe ◽  
Phase Coexistence ◽  
Potassium Sodium Niobate ◽  
Diffraction Patterns ◽  
Scanning Electron

The origin of the complex reflection splitting in potassium sodium niobate doped with lithium and manganese was investigated using temperature-dependent high-resolution X-ray and neutron diffraction as well as electron probe microanalysis and scanning electron microscopy. Two structural models were developed from the diffraction data. A single-phase monoclinic Pm model is known from the literature and is able to reproduce the diffraction patterns perfectly. However, a model with phase coexistence of two classical orthorhombic Amm2 phases can also reproduce the diffraction data with equal accuracy. Scanning electron microscopy in combination with electron probe microanalysis revealed segregation of the A-site substituents potassium and sodium. This favours the model with phase coexistence and confirms the need for comprehensive analyses with complementary methods to cover a broad range of length scales as well as to assess both average and local structure.

High Resolution Scanning Electron Microscopy

1991 ◽  
Vol 49 ◽  
pp. 478-479
Author(s):  
David Joy ◽  
James Pawley
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Electron Beam ◽  
Electron Microscope ◽  
High Resolution ◽  
Scanning Electron Microscope ◽  
Electron Probe ◽  
Impact Point ◽  
Interaction Volume ◽  
Scanning Electron

The scanning electron microscope (SEM) builds up an image by sampling contiguous sub-volumes near the surface of the specimen. A fine electron beam selectively excites each sub-volume and then the intensity of some resulting signal is measured. The spatial resolution of images made using such a process is limited by at least three factors. Two of these determine the size of the interaction volume: the size of the electron probe and the extent to which detectable signal is excited from locations remote from the beam impact point. A third limitation emerges from the fact that the probing beam is composed of a finite number of discrete particles and therefore that the accuracy with which any detectable signal can be measured is limited by Poisson statistics applied to this number (or to the number of events actually detected if this is smaller).

An emendation of the generic diagnosis of Phoreiobothrium Linton, 1889 (Tetraphyllidea: Onchobothriidae) with a detailed description of bothridia and hooks

1985 ◽  
Vol 63 (5) ◽  
pp. 1199-1206 ◽  
Author(s):  
J. N. Caira
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Monophyletic Group ◽  
Generic Diagnosis ◽  
The Third ◽  
Scanning Electron

Hook terminology for the three-pronged hooks of Phoreiobothrium Linton, 1889 is reconciled with that for two-pronged hooks such that the two outermost prongs are considered homologous with the prongs of a two-pronged hook and the third inner prong is termed the basal prong. Scanning electron microscopy was performed on the scolex of Phoreiobothrium lasium Linton, 1889 and the solid nature of the bothridia was reconfirmed. Examination of material of all four species of Phoreiobothrium leads to the conclusion that each species possesses three-pronged hooks that are hollow and open to the outside via pores. The bothridia of each species are considered to be horizontally divided into two loculi, the posterior one being recessed and vertically subdivided. The diagnosis of the genus Phoreiobothrium is emended, and the four species allocated to it are redescribed. Phoreiobothrium is determined to be a monophyletic group on the basis of two synapomorphies and a key to the four species of the genus is presented.

Evaluation of computer-controlled SEM in the study of metal-contaminated soils

2003 ◽  
Vol 67 (2) ◽  
pp. 219-231 ◽  
Author(s):  
H. W. Langmi ◽  
J. Watt
Keyword(s):  
Electron Microscopy ◽  
Heavy Metals ◽  
Contaminated Soils ◽  
X Ray ◽  
Computer Controlled ◽  
Weathering Crusts ◽  
Individual Particles ◽  
Element Mapping ◽  
Scanning Electron

Computer-controlled scanning electron microscopy (CCSEM) has been assessed for the determination of form and size distribution of heavy metals in urban contaminated soils. Metal distributions within individual particles were determined using X-ray element mapping. The sites selected for study were (1) around a landfill site, previously a colliery in Wolverhampton, UK and (2) a private garden adjacent to a railway in Nottingham, UK. Backscattered thresholding techniques were used to isolate the Pb-containing categories. The classification results for both Wolverhampton and Nottingham soils were generally similar but more Pb-containing classes were observed for the Nottingham samples when a comparison was made between results of the same size fractions. However, difficulties with the technique arose when particles showing chemically similar weathering crusts were assigned to the same class, despite having different internal compositions. The CCSEM data therefore need to be interpreted with caution and their application limited to situations in which particle internal complexity is not an issue.

The Mechanism of active capture of animal food by the Sergestid Shrimp Acetes Sibogae Australis

1998 ◽  
Vol 78 (2) ◽  
pp. 497-508 ◽  
Author(s):  
Lachlan Mcleay ◽  
C.G. Alexander
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Prey Capture ◽  
Size Range ◽  
The Third ◽  
Feeding Modes ◽  
In Captivity ◽  
Combined Actions ◽  
Wide Size Range ◽  
Scanning Electron

Combining the use of scanning electron microscopy and microcinematography with functional and behavioural observations has clarified many aspects underlying the feeding processes of the small planktonic sergestid shrimp Acetes sibogae australis. In captivity Acetes sibogae australis is an opportunistic feeder that uses four principal feeding modes to capture a wide size range of prey: Artemia nauplii (<0.33 mm), copepods (<1mm) and moribund Acetes (up to 25 mm). Prey capture is effected by combined actions of the first three pairs of pereiopods and the third maxillipeds before transfer to the more dorsal second maxillipeds. The second maxillipeds are the principal appendages used in securing, manipulating, sorting and rejecting prey before insertion into the vicinity of the inner mouthparts.

scholarly journals The use of scanning electron microscopy to the study of the painting from the Church in Radcze

2013 ◽  
Vol 12 (4) ◽  
pp. 095-105
Author(s):  
Beata Klimek
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Electron Microscope ◽  
Historic Buildings ◽  
X Ray ◽  
Composition And Structure ◽  
The Church ◽  
Diagnosis Technique ◽  
Scanning Electron

One of the main tasks in the study of historic buildings is the need to identify the original materials and extensions, which often have historic character. The next task concerns the determination of the composition and structure of the historical, diagnosis technique to develop original paint. The article presents the preliminary results of paintings. Methods were used with the scanning electron microscope was equipped with an energy dispersive X-ray spectrometer (SEM-EDS).

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