Martensitic Transformation in Mn-Ni-Sn Alloys

2013 ◽  
Vol 738-739 ◽  
pp. 468-472
Author(s):  
R. Coll ◽  
J. Bonastre ◽  
J. Saurina ◽  
J.J. Suñol ◽  
L. Escoda ◽  
...  
Keyword(s):  
Martensitic Transformation ◽  
Diffraction Analysis ◽  
Structural Transformation ◽  
Tetragonal Phase ◽  
Melt Spinning ◽  
Monoclinic Phase ◽  
X Ray Diffraction ◽  
Transformation Temperatures ◽  
X Ray ◽  
A Minor

In this work, we analyze two Mn50Ni50-xSnx alloys with Sn content i.e., x = 5 and 7.5 respectively. These alloys are produced as ribbon-shape by melt spinning. Their structural transformation is checked by calorimetry. Martensitic transformation temperatures of these alloys strongly depend on the composition. From X-ray diffraction analysis, the 14M monoclinic phase is the main phase in both alloys, but in the alloy Sn5 appears a minor tetragonal phase too.

Texture on Ground, Fractured, and Aged Y-TZP Surfaces

1986 ◽  
Vol 78 ◽  
Author(s):  
Franz Reidinger ◽  
Philip J. Whalen
Keyword(s):  
Phase Composition ◽  
Transition Temperature ◽  
Diffraction Analysis ◽  
Surface Treatment ◽  
Tetragonal Phase ◽  
Surface Region ◽  
X Ray Diffraction ◽  
X Ray ◽  
History Of

ABSTRACTThe phase composition of Y-TZP surfaces has been shown to vary greatly depending on the thermo-mechanical history of the surface. The orientation of these different phases in the surface region is not always random. There is speculation that the alignment of the tetragonal phase before fracturing may play a part in increasing the toughness of these materials. This article deals with an X-ray diffraction analysis of various Y-TZP surfaces with special emphasis on the texture of the different phases. Surfaces which have been ground (and polished), fractured, and aged (200°C) have been examined. In all cases, the monoclinic component that was formed was strongly oriented. The tetragonal phase may or may not be oriented depending on surface treatment. Annealing above the monoclinic-tetragonal transition temperature had little effect on the tetragonal orientation in most cases. Samples fractured at 1000°C have no unusual orientation on the fracture faces.

Pseudo-Elastic Behaviour in Rapidly-Quenched Dilute Tin Alloys

1981 ◽  
Vol 8 ◽  
Author(s):  
W.M. Callernfault ◽  
R.W. Smith
Keyword(s):  
Martensitic Transformation ◽  
Melt Spinning ◽  
Elastic Behaviour ◽  
X Ray Diffraction ◽  
Tin Alloys ◽  
X Ray ◽  
Dilute Alloys ◽  
Copper Cylinder

ABSTRACTRibbons of pure tin (99.9999%) and dilute Sn-Ge alloys, prepared by melt spinning using a 4′ diameter copper cylinder, were strained in tension. Reversible strains of a few percent were recorded in the dilute alloys but not in the pure tin. X-ray diffraction examination suggests that this pseudoelasticity is due to twinning rather than a martensitic transformation.

B(C6F5)3-guided cyclotrimerization-rearrangement of phenylacetylene. Evidence of the (C6F5)3B−–C(H)=C+Ph intermediate in a 1,1-carboboration reaction

2016 ◽  
Vol 71 (10) ◽  
pp. 1029-1041
Author(s):  
Wanli Nie ◽  
Guofeng Sun ◽  
Chong Tian ◽  
Maxim V. Borzov
Keyword(s):  
Nmr Spectroscopy ◽  
Diffraction Analysis ◽  
Crystal Structures ◽  
Variable Temperature ◽  
Spectroscopy Study ◽  
X Ray Diffraction ◽  
X Ray ◽  
Spectral Evidence ◽  
A Minor ◽  
Zwitterionic Intermediate

AbstractIn presence of 2,2,6,6-tetramethylpiperidinium ([TMPH]+) chlorotris(pentafluorophenyl)borate ([TMPH]+[ClB(C6F5)3]−, 3), phenylacetylene undergoes an unusual cyclotrimerization-rearrangement leading to tris(pentafluorophenyl)(3,4,5-triphenylphenyl)borate anion (1) as a minor product which can be isolated and purified in a form of salts [1·(TMPH)n·Cl(n–1)] (n=3 or 5). A variable temperature and concentration NMR spectroscopy study of 3 in CDCl3 unambiguously demonstrated its ability to liberate free B(C6F5)3, which initiates cyclotrimerization and guides rearrangements towards formation of the tetraarylborate anion 1. For the previously studied “spectator” reaction between phenylacetylene and B(C6F5)3 in CDCl3, 1H, 19F, and 11B NMR-spectral evidence of the (C6F5)3B−–C(H)=C+Ph zwitterionic intermediate of the 1,1-carboboration reaction has been demonstrated. The crystal structures of [1·(TMPH)3·Cl2], the salt 3, and a 1:1 adduct of 1,3,5-tris(4-fluorophenyl)benzene and 2,4,6-tris(pentafluorophenyl)-1,3,5,2,4,6-trioxatriborinane (2) have been established by X-ray diffraction analysis.

Effect of Cooling Rate on the Transformation Temperatures of Ni50Ti36Hf14 Melt-Spun Ribbons

2018 ◽  
Vol 930 ◽  
pp. 345-348
Author(s):  
R.L. Soares ◽  
Walman Benicio Castro
Keyword(s):  
Differential Scanning Calorimetry ◽  
Martensitic Transformation ◽  
Cooling Rate ◽  
Melt Spinning ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Melt Spun ◽  
Melt Spun Ribbons ◽  
Memory Characteristics

Solidification structures and shape memory characteristics of Ni50Ti36Hf14(at.%) alloy ribbons prepared by melt spinning were investigated by means of differential scanning calorimetry and X-ray diffraction. In these experiments particular attention has been paid to change the velocity of cooling wheel from 20 to 40 m/s. Then the cooling rates of ribbons were controlled. The effect of this cooling rate on solidification structures and martensitic transformation behaviors is discussed. When the ribbon is produced at a wheel velocity of 40 m/s in melt spinning, the degree of supercooling becomes high because of its thinner thickness.

Microdomains in BaFeO3-y (0.35 < y < 0.50)

1990 ◽  
Vol 48 (4) ◽  
pp. 780-781
Author(s):  
M. Vallet-Regí ◽  
M. Parras ◽  
J.M. González-Calbet ◽  
J.C. Grenier
Keyword(s):  
Electron Diffraction ◽  
Chemical Analysis ◽  
Monoclinic Phase ◽  
Orthorhombic Phase ◽  
Total Iron ◽  
Zone Axis ◽  
Electron Micrograph ◽  
X Ray Diffraction ◽  
X Ray ◽  
Compositional Variations

BaFeO3-y compositions (0.35<y<0.50) have been investigated by means of electron diffraction and microscopy to resolve contradictory results from powder X-ray diffraction data.The samples were obtained by annealing BaFeO2.56 for 48 h. in the temperature range from 980°C to 1050°C . Total iron and barium in the samples were determined using chemical analysis and gravimetric methods, respectively.In the BaFeO3-y system, according to the electron diffraction and microscopy results, the nonstoichiometry is accommodated in different ways as a function of the composition (y):In the domain between BaFeO2.5+δBaFeO2.54, compositional variations are accommodated through the formation of microdomains. Fig. la shows the ED pattern of the BaFeO2.52 material along thezone axis. The corresponding electron micrograph is seen in Fig. 1b. Several domains corresponding to the monoclinic BaFeO2.50 phase, intergrow with domains of the orthorhombic phase. According to that, the ED pattern of Fig. 1a, can be interpreted as formed by the superposition of three types of diffraction maxima : Very strong spots corresponding to a cubic perovskite, a set of maxima due to the superposition of three domains of the monoclinic phase along [100]m and a series of maxima corresponding to three domains corresponding to the orthorhombic phase along the [100]o.

Ten-Vertex Polyhedral Monocarbaborane Chemistry. The Novel High-Yield Formation of the Ten-Vertex closo Compound [6-(PMe2Ph)-closo-1-CB9H9] from the Thermolysis of [8,8-(PMe2Ph)2-nido-8,7-PtCB9H11]

1993 ◽  
Vol 58 (12) ◽  
pp. 2924-2935 ◽  
Author(s):  
Jane H. Jones ◽  
Bohumil Štíbr ◽  
John D. Kennedy ◽  
Mark Thornton-Pett
Keyword(s):  
Nmr Spectroscopy ◽  
Diffraction Analysis ◽  
High Yield ◽  
Monoclinic Space Group ◽  
The Novel ◽  
X Ray Diffraction ◽  
Metal Centre ◽  
X Ray ◽  
Yield Formation ◽  
Boiling Toluene

Thermolysis of [8,8-(PMe2Ph)2-nido-8,7-PtCB9H11] in boiling toluene solution results in an elimination of the platinum centre and cluster closure to give the ten-vertex closo species [6-(PMe2Ph)-closo-1-CB9H9] in 85% yield as a colourles air stable solid. The product is characterized by NMR spectroscopy and single-crystal X-ray diffraction analysis. Crystals (from hexane-dichloromethane) are monoclinic, space group P21/c, with a = 903.20(9), b = 1 481.86(11), c = 2 320.0(2) pm, β = 97.860(7)° and Z = 8, and the structure has been refined to R(Rw) = 0.045(0.051) for 3 281 observed reflections with Fo > 2.0σ(Fo). The clean high-yield elimination of a metal centre from a polyhedral metallaborane or metallaheteroborane species is very rare.

Bis(μ-carboxylato)dienerhodium(I) Complexes - Synthesis, Characterization and Catalytic Activity

2008 ◽  
Vol 73 (8-9) ◽  
pp. 1205-1221 ◽  
Author(s):  
Jiří Zedník ◽  
Jan Sedláček ◽  
Jan Svoboda ◽  
Jiří Vohlídal ◽  
Dmitrij Bondarev ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Diffraction Analysis ◽  
Spectroscopic Methods ◽  
X Ray Diffraction ◽  
X Ray

Dinuclear rhodium(I) η2:η2-cycloocta-1,5-diene (series a) and η2:η2-norborna-2,5-diene (series b) complexes with μ-RCOO- ligands, where R is linear C21H43 (complexes 1a, 1b), CH2CMe3 (2a, 2b), 1-adamantyl (3a, 3b) and benzyl (4a, 4b), have been prepared and characterized by spectroscopic methods. Structures of complexes 2b, 3a and 4a were determined by X-ray diffraction analysis. Complexes prepared show low to moderate catalytic activity in polymerization of phenylacetylene in THF giving high-cis-transoid polymers, but they show only oligomerization activity in dichloromethane.

Sign in / Sign up

Export Citation Format

Share Document