Microstructure of Electro-Eroded Cemented Carbide Surfaces

1968 ◽  
Vol 26 ◽  
pp. 284-285
Author(s):  
V. N. Filimonenko ◽  
M. H. Richman ◽  
J. Gurland
Keyword(s):  
Surface Layer ◽  
Cobalt Content ◽  
Cemented Carbides ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Metallographic Examination ◽  
Standard Procedures ◽  
Face Centered ◽  
Diamond Paste ◽  
Plastic Carbon

The high temperatures and pressures that are found in a spark gap during electrical discharging lead to a sharp phase transition and structural transformation in the surface layer of cemented carbides containing WC and cobalt. By means of X-ray diffraction both W2C and a high-temperature monocarbide of tungsten (face-centered cubic) were detected after electro-erosion. The W2C forms as a result of the peritectic reaction, WC → W2C+C. The existence and amount of the phases depend on both the energy of the electro-spark discharge and the cobalt content. In the case of a low-energy discharge (i.e. C=0.01μF, V = 300v), WC(f.c.c.) is generally formed in the surface layer. However, at high energies, (e.g. C=30μF, V = 300v), W2C is formed at the surface in preference to the monocarbide. The phase transformations in the surface layer are retarded by the presence of larger percentages of cobalt.Metallographic examination of the electro-eroded surfaces of cemented carbides was carried out on samples with 5-30% cobalt content. The specimens were first metallographically polished using diamond paste and standard procedures and then subjected to various electrical discharges on a Servomet spark machining device. The samples were then repolished and etched in a 3% NH4OH electrolyte at -0.5 amp/cm2. Two stage plastic-carbon replicas were then made and shadowed with chromium at 27°.

Depletion of Manganese in the Surface Layers of Fe-Mn-Si Shape Memory Alloys by Annealing

2015 ◽  
Vol 363 ◽  
pp. 196-201
Author(s):  
Yusuke Onuki ◽  
Shun Fujieda ◽  
Kozo Shinoda ◽  
Hiroshi Ohtani ◽  
Tadakatsu Maruyama ◽  
...  
Keyword(s):  
Surface Layer ◽  
Shape Memory Alloys ◽  
Shape Memory ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Surface Layers ◽  
Hexagonal Close Packed ◽  
Compositional Changes ◽  
Face Centered ◽  
The Stability

X-ray diffraction (XRD) and electron microprobe microanalysis (EPMA) were used for characterizing the structure and composition of surface layers formed on austenitic Fe-Mn-Si shape memory alloys under vacuum. The XRD results demonstrated that during annealing, face centered cubic austenite is transformed to hexagonal close packed martensite on the alloy surface. The EMPA results revealed that manganese in the surface layer was depleted during annealing. Further, this analysis determined that the thickness of the surface layer of the alloy annealed at 1173 K for 1 h was approximately 20 μm and that value is consistent with the depth detected by XRD. The compositional changes of the surface layers such as manganese depletion by annealing were discussed based on the ternary Fe-Mn-Si phase diagram. Although the formation of body centered cubic ferrite is detrimental to shape memory alloys, the amount of manganese was also observed to change during processing and strongly influence the stability of the shape memory alloys.

Stacking Faults in a High Nitrogen Face-Centered-Cubic Phase Formed on Nitrogen-Modified Austenitic Stainless Steel

2008 ◽  
Vol 373-374 ◽  
pp. 318-321
Author(s):  
J. Liang ◽  
M.K. Lei
Keyword(s):  
Stainless Steel ◽  
Plasma Source ◽  
Peak Shift ◽  
Cubic Phase ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
High Nitrogen ◽  
X Ray ◽  
Peak Asymmetry ◽  
Face Centered

Effects of stacking faults in a high nitrogen face-centered-cubic phase (γΝ) formed on plasma source ion nitrided 1Cr18Ni9Ti (18-8 type) austenitic stainless steel on peak shift and peak asymmetry of x-ray diffraction were investigated based on Warren’s theory and Wagner’s method, respectively. The peak shift from peak position of the γΝ phase is ascribed to the deformation faults density α, while the peak asymmetry of the γΝ phase is characterized by deviation of the center of gravity of a peak from the peak maximum (Δ C.G.) due to the twin faults density β. The calculated peak positions of x-ray diffraction patterns are consistent with that measured for plasma source ion nitrided 1Cr18Ni9Ti stainless steel.

scholarly journals Characterization of Cobalt Sulfide Thin Films Synthesized from Acidic Chemical Baths

2020 ◽  
Vol 2020 ◽  
pp. 1-9
Author(s):  
Tizazu Abza ◽  
Dereje Gelanu Dadi ◽  
Fekadu Gashaw Hone ◽  
Tesfaye Chebelew Meharu ◽  
Gebremeskel Tekle ◽  
...  
Keyword(s):  
Thin Films ◽  
Crystallite Size ◽  
Deposition Time ◽  
Average Crystallite Size ◽  
Cobalt Sulfide ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
Face Centered

Cobalt sulfide thin films were synthesized from acidic chemical baths by varying the deposition time. The powder X-ray diffraction studies indicated that there are hexagonal CoS, face-centered cubic Co3S4, and cubic Co9S8 phases of cobalt sulfide. The crystallite size of the hexagonal CoS phase decreased from 52.8 nm to 22.5 nm and that of the cubic Co9S8 phase increased from 11 nm to 60 nm as the deposition time increased from 2 hrs to 3.5 hrs. The scanning electron microscopic images revealed crack and pinhole free thin films with uniform and smooth background and few large polygonal grains on the surface. The band gap of the cobalt sulfide thin films decreased from 1.75 eV to 1.3 eV as the deposition time increased from 2 hrs to 3.5 hrs. The photoluminescence (PL) spectra of the films confirmed the emission of ultraviolet, violet, and blue lights. The intense PL emission of violet light at 384 nm had red shifted with increasing deposition time that could be resulted from the increase in the average crystallite size. The FTIR spectra of the films indicated the presence of OH, C-O-H, C-O, double sulfide, and Co-S groups. As the deposition time increased, the electrical resistivity of the cobalt sulfide thin films decreased due to the increase in both the crystallite size and the films’ thickness.

Theoretical and experimental study of the gradient properties and the resulting local crystalline structure and orientation in magnetron-sputtered CrAlN coatings with lateral composition and thickness gradient

2017 ◽  
Vol 50 (4) ◽  
pp. 1000-1010
Author(s):  
Bärbel Krause ◽  
Michael Stüber ◽  
Anna Zimina ◽  
Ralph Steininger ◽  
Mareike Trappen ◽  
...  
Keyword(s):  
Target Surface ◽  
Sample Surface ◽  
Composition Gradient ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
X Ray ◽  
Al Content ◽  
Spatially Resolved ◽  
Composition Profiles ◽  
Face Centered

Cr–Al–N coatings with a lateral composition gradient were deposited from two segmented Cr/Al targets with different segment size, thus covering the Al content range 0.22 ≲ c ≲ 0.87 and a thickness range from several hundred nanometres to several micrometres. The two-dimensional thickness and composition profiles were determined nondestructively from X-ray fluorescence maps. The results were reproduced by simulations of the flux distribution on the sample surface, combiningTRIDYNsimulations of the reactive sputter process at the target surface andSIMTRAsimulations of the subsequent transport through the gas phase. The phase formation was studied by spatially resolved X-ray diffraction and X-ray absorption spectroscopy at the Cr Kedge. Forc ≲ 0.69, a single-phase solid solution face-centered cubic (f.c.c.) (Cr,Al)N phase was found, and for 0.69 ≲ c ≲ 0.87 coexisting f.c.c. (Cr,Al)N and hexagonal close packed (h.c.p.) (Cr,Al)N phases were observed. The biaxial texture formation in nearly the entire composition range indicates a zone T growth. Four, mainly composition-dependent, texture regions were identified. All observed textures are closely related to textures reported for the h.c.p. AlN and f.c.c. CrN parent phases. Forc ≳ 0.69, a strong thickness dependence of the textures was observed. The measurements reveal an orientation relation between different f.c.c. and h.c.p. textures, indicating that local epitaxy might play a role in the structure formation.

Thermal Stability and Failure Mechanisms of Au/Tiw(N)/Si and Au/TiW(N)/Si02/Si Systems

1996 ◽  
Vol 427 ◽  
Author(s):  
C. R. Chen ◽  
L. J. Chen
Keyword(s):  
Thermal Stability ◽  
Failure Mechanisms ◽  
Cubic Phase ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Single Face ◽  
Face Centered ◽  
The Stability ◽  
Ar Gas

AbstractThermal stability and failure mechanisms of Au/TiW(N)/Si and Au/TiW(N)/SiO2/Si systems have been studied by both conventional and high-resolution transmission electron microscopy, X- ray diffraction and Auger electron spectroscopy. For films deposited in Ar gas containing 20% N2, a single face-centered-cubic phase was the only crystalline phase detected to form. The samples were found to remain stable after annealing at 700 °C for 30 min. The stability temperature for Au/TiW(N)(Ar:N2=80:20)/SiO2/Si samples was found to be higher than those of Au/TiW(N) (Ar:N2=90:10)/SiO2/Si and Au/TiW/SiO2/Si samples.

Structural, morphological, and magnetic study of nanocrystalline cobalt-copper powders synthesized by the polyol process

1995 ◽  
Vol 10 (6) ◽  
pp. 1546-1554 ◽  
Author(s):  
G.M. Chow ◽  
L.K. Kurihara ◽  
K.M. Kemner ◽  
P.E. Schoen ◽  
W.T. Elam ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Copper Powders ◽  
Face Centered ◽  
Increasing Temperature ◽  
X Ray Absorption

Nanocrystalline CoxCu100−x (4 ⋚ x ⋚ 49 at. %) powders were prepared by the reduction of metal acetates in a polyol. The structure of powders was characterized by x-ray diffraction (XRD), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), extended x-ray absorption fine structure (EXAFS) spectroscopy, solid-state nuclear magnetic resonance (NMR) spectroscopy, and vibrating sample magnetometry (VSM). As-synthesized powders were composites consisting of nanoscale crystallites of face-centered cubic (fcc) Cu and metastable face-centered cubic (fcc) Co. Complementary results of XRD, HRTEM, EXAFS, NMR, and VSM confirmed that there was no metastable alloying between Co and Cu. The NMR data also revealed that there was some hexagonal-closed-packed (hcp) Co in the samples. The powders were agglomerated, and consisted of aggregates of nanoscale crystallites of Co and Cu. Upon annealing, the powders with low Co contents showed an increase in both saturation magnetization and coercivity with increasing temperature. The results suggested that during preparation the nucleation of Cu occurred first, and the Cu crystallites served as nuclei for the formation of Co.

scholarly journals Pressure-Induced Dimerization of C60 at Room Temperature as Revealed by an In Situ Spectroscopy Study Using an Infrared Laser

Crystals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 182 ◽  
Author(s):  
Bing Li ◽  
Jinbo Zhang ◽  
Zhipeng Yan ◽  
Meina Feng ◽  
Zhenhai Yu ◽  
...  
Keyword(s):  
Room Temperature ◽  
Infrared Laser ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Simple Cubic ◽  
Excitation Laser ◽  
Face Centered ◽  
830 Nm Laser ◽  
Structure Evaluation

Using in situ high-pressure Raman spectroscopy and X-ray diffraction, the polymerization and structure evaluation of C60 were studied up to 16 GPa at room temperature. The use of an 830 nm laser successfully eliminated the photo-polymerization of C60, which has interfered with the pressure effect in previous studies when a laser with a shorter wavelength was used as excitation. It was found that face-centered cubic (fcc) structured C60 transformed into simple cubic (sc) C60 due to the hint of free rotation for the C60 at 0.3 GPa. The pressure-induced dimerization of C60 was found to occur at about 3.2 GPa at room temperature. Our results suggest the benefit and importance of the choice of the infrared laser as the excitation laser.

Photocatalytic Analysis and Characterization of Zn2SnO4 Nanoparticles Synthesized via Hydrothermal Method with Na2CO3 Mineralizer

2010 ◽  
Vol 97-101 ◽  
pp. 19-22 ◽  
Author(s):  
Yu Shiang Wu ◽  
Wen Ku Chang ◽  
Min Jou
Keyword(s):  
Photocatalytic Activity ◽  
Hydrothermal Process ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
Transmission Electron ◽  
Excellent Photocatalytic Activity ◽  
Face Centered ◽  
Xrd Patterns

Zinc stannate Zn2SnO4 (ZTO) nanoparticles were synthesized via a hydrothermal process utilizing sodium carbonate (Na2CO3) as a weak basic mineralizer. The samples were hydrothermally treated at 150, 200, and 250oC for 48 h. The X-ray diffraction (XRD) patterns show that the highly-crystalline ZTO nanostructure could be formed in a well-dispersed manner for the 250°C sample at a particle size of less than 50 nm. As determined from transmission electron microscopy (TEM) results, ZTO nanoparticles are face-centered cubic single crystals agglomerated together. The Raman spectra results showed that the ZTO nanocrystals have a spinel structure. Furthermore, photocatalytic activity was tested with methylene blue (MB) by UV irradiation. The ZTO synthesized by the 2 M Na2CO3 mineralizer at 250oC demonstrated excellent photocatalytic activity. The ZTO treated three different ways had three distinct UV-Visible absorption curves, which directly influences their corresponding photocatalytic activity.

Plastic Deformation of Nanometric Grinding Process for FCC Metal

2010 ◽  
Vol 154-155 ◽  
pp. 1336-1341
Author(s):  
Wei Wen Zhang ◽  
Gang Guo ◽  
Yun Huang ◽  
Zhi Huang
Keyword(s):  
Plastic Deformation ◽  
Surface Layer ◽  
Grinding Process ◽  
Face Centered Cubic ◽  
Grinding Processes ◽  
Cubic Structure ◽  
Simulation Results ◽  
Face Centered ◽  
Dislocation Defects ◽  
Fcc Metal

This paper focuses on the simulations of nanometric grinding process on face centered cubic structure (FCC) single metal crystals (Cu, Ni) using Molecular dynamics. In order to analyze the plastic deformation of sample metals in nanometric grinding processes, we propose an approach using techniques of central symmetry parameters and neighbor changing ratios. The simulation results show that besides the normal dislocation defects, weak slipping defects locating on {111} crystal planes are found under the surface layer. In addition, the distribution of the neighbor changing ratio indicates that the nano grinding processes will likely cause the global plastic deformation in the surface layer.

Synthesis and Characterization of Cobalt-Nickel Nanowires Formed under External Magnetic Field

2015 ◽  
Vol 799-800 ◽  
pp. 120-124 ◽  
Author(s):  
Mary Donnabelle L. Balela ◽  
Lalaine M. Dulin ◽  
Erica A. Garcia ◽  
M. Janelle H. Tica
Keyword(s):  
Magnetic Field ◽  
External Magnetic Field ◽  
Face Centered Cubic ◽  
X Ray Diffraction ◽  
X Ray ◽  
Hexagonal Close Packed ◽  
Cobalt Nickel ◽  
Nickel Nanowires ◽  
Face Centered

Cobalt-nickel (Co-Ni) nanowires were formed by electroless deposition in ethylene glycol under external magnetic field. The effects of initial Co (II) and Ni (II) concentration on the surface and morphology of the synthesized nanowires were investigated by x-ray diffraction (XRD) and scanning electron microscope (SEM) respectively. An increase in the Co (II) concentration resulted in increase in diameter of the nanowires. However, the length of nanowires was observed to decrease. Higher Co (II) concentration resulted in a mixture of hexagonal close-packed and face-centered cubic Co-Ni nanowires. X-ray diffraction revealed that crystal growth occurred when the nanowires are annealed at 653 K for 10h.

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