X-Ray Stress Studies of Passivated and Unpassivated Narrow Aluminum Metallizations

1990 ◽  
Vol 188 ◽  
Author(s):  
C. A. Paszkiet ◽  
M. A. Korhonen ◽  
Che-Yu Li

ABSTRACTStresses in thin narrow textured metal lines were measured using x-ray diffraction techniques. Arrays of 1.5μm wide, 0.32μm thick aluminum lines, both with and without a 0.32μm thick SiNx passivation layer, were heat-treated at 400°C in a hydrogen/nitrogen atmosphere. After heat treatment the lines were examined periodically using chromium radiation to monitor the relaxation of the stress developed during heat treatment. The apparent stress in both the passivated and unpassivated lines relaxed significantly over the measurement period of three days. The higher stresses present in the passivated lines may be partially responsible for the voids which were found after aging at room temperature.

2006 ◽  
Vol 530-531 ◽  
pp. 197-202 ◽  
Author(s):  
Alfeu Saraiva Ramos ◽  
Erika Coaglia Trindade Ramos ◽  
Carlos de Moura Neto

The present work reports on the preparation of the Ta5SiB2 compound by highenergy ball milling and subsequent heat treatment from elemental Ta-12.5at%Si-25at%B powder mixture. The milling process was carried out at room temperature in a planetary ball mill under argon atmosphere. Following the milling process, the powders were heat-treated at 1200oC for 4h under Ar atmosphere in order to obtain the equilibrium microstructure. The milled and heat-treated powders were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Results indicated that the Si peaks disappeared after milling for 1h. It was noted that the broadening and the reduced intensity of Ta peaks occurred continuously up to milling for 10h, suggesting that the Si and B atoms were preferentially dissolved into the Ta lattice during ball milling to form a supersaturated solid solution. A halo was formed in Ta-12.5at%Si-25at%B powders milled for 100h, suggesting that an amorphous phase was achieved. No intermetallic phase was formed in powders milled for 200h. A large amount of Ta5SiB2 was formed after heat treatment at 1200oC for 4h. In addition, peaks of TaB and another unknown phase were also identified.


2021 ◽  
Author(s):  
Mei Yang ◽  
Yishu Zhang ◽  
Haoxing You ◽  
Richard Smith ◽  
Richard D. Sisson

Abstract Selective laser melting (SLM) is an additive manufacturing technique that can be used to make the near-net-shape metal parts. M2 is a high-speed steel widely used in cutting tools, which is due to its high hardness of this steel. Conventionally, the hardening heat treatment process, including quenching and tempering, is conducted to achieve the high hardness for M2 wrought parts. It was debated if the hardening is needed for additively manufactured M2 parts. In the present work, the M2 steel part is fabricated by SLM. It is found that the hardness of as-fabricated M2 SLM parts is much lower than the hardened M2 wrought parts. The characterization was conducted including X-ray diffraction (XRD), optical microscopy, Scanning Electron Microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS) to investigate the microstructure evolution of as-fabricated, quenched, and tempered M2 SLM part. The M2 wrought part was heat-treated simultaneously with the SLM part for comparison. It was found the hardness of M2 SLM part after heat treatment is increased and comparable to the wrought part. Both quenched and tempered M2 SLM and wrought parts have the same microstructure, while the size of the carbides in the wrought part is larger than that in the SLM part.


2006 ◽  
Vol 118 ◽  
pp. 53-58
Author(s):  
Elisabeth Meijer ◽  
Nicholas Armstrong ◽  
Wing Yiu Yeung

This study is to investigate the crystallite development in nanostructured aluminium using x-ray line broadening analysis. Nanostructured aluminium was produced by equal channel angular extrusion at room temperature to a total deformation strain of ~17. Samples of the extruded metal were then heat treated at temperatures up to 300oC. High order diffraction peaks were obtained using Mo radiation and the integral breadth was determined. It was found that as the annealing temperature increased, the integral breadth of the peak reflections decreased. By establishing the modified Williamson-Hall plots (integral breadth vs contract factor) after instrumental correction, it was determined that the crystallite size of the metal was maintained ~80 nm at 100oC. As the annealing temperature increased to 200oC, the crystallite size increased to ~118 nm. With increasing annealing temperature, the hardness of the metal decreased from ~60 HV to ~45 HV.


2018 ◽  
Vol 25 (08) ◽  
pp. 1950023 ◽  
Author(s):  
ARKADEB MUKHOPADHYAY ◽  
TAPAN KUMAR BARMAN ◽  
PRASANTA SAHOO

The present work reports the deposition of a quaternary Ni-B-W-Mo coating on AISI 1040 medium carbon steel and its characterization. Quaternary deposits are obtained by suitably modifying existing electroless Ni-B bath. Composition of the as-deposited coating is analyzed by energy dispersive X-ray spectroscopy. The structural aspects of the as-deposited and coatings heat treated at 300[Formula: see text]C, 350[Formula: see text]C, 400[Formula: see text]C, 450[Formula: see text]C and 500[Formula: see text]C are determined using X-ray diffraction technique. Surface of the as-deposited and heat-treated coatings is examined using a scanning electron microscope. Very high W deposition could be observed when sodium molybdate is present in the borohydride-based bath along with sodium tungstate. The coatings in their as-deposited condition are amorphous while crystallization takes place on heat treatment. A nodulated surface morphology of the deposits is also observed. Vickers’ microhardness and crystallite size measurement reveal inclusion of W and Mo results in enhanced thermal stability of the coatings. Solid solution strengthening of the electroless coatings by W and Mo is also observed. The applicability of kinetic strength theory to the hardening of the coatings on heat treatment is also investigated. Corrosion resistance of Ni-B-W-Mo coatings and effect of heat treatment on the same are also determined by electrochemical techniques.


Materials ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 1883 ◽  
Author(s):  
Chao Peng ◽  
Guangxue Chen

In this study, poly(vinyl alcohol) (PVA) composite films enhanced by α-chitin nanowhiskers (ChWs) were prepared through heat treatment. The obtained membranes were assessed by means of FTIR spectroscopy, X-ray diffraction, thermogravimetric analysis, regular light transmittance, mechanical tests, permeability and water absorption. The influence of the nano-component and heat treatment on the mechanical, thermal and water-resistant properties of the composite membrane were analyzed. From the results of the work, the produced films with excellent barrier properties and inexpensive raw processed materials have great prospects in packaging applications.


2021 ◽  
Vol 1016 ◽  
pp. 1299-1304
Author(s):  
Naidu Seetala ◽  
Deidre Henderson ◽  
Jumel Jno-Baptiste ◽  
Hao Wen ◽  
Sheng Min Guo

The microstructure and magnetization of SmCo5 micro-particles may be used as feedstock for 3D printing to make miniature strong magnets. Thus, the magnetic response and microstructures of commercially available SmCo5 micro-particles were studied under various heat treatments using a high wattage laser. The magnetization of laser heat treated powders at 50-watt showed an increase in magnetization, while the 75-watt melt showed a little to no change. Unfortunately, the coercivity of both laser heat treated samples decreased significantly. Oxidation during the heat treatment is suspected to result in low coercivity. Purging with argon-gas prior to laser heating showed improved coercivity. To further minimize the oxidation problem a set of SmCo5 powder was reduced prior to laser heat treatment using a constant flow of hydrogen gas while being heated at various temperatures from 100 oC to 400 oC for a period of ~4 hours. The results show that the magnetization generally increases with the temperature, while the coercivity decreases significantly. Another set of SmCo5 was annealed in a vacuum furnace for one hour at temperatures between 200 oC and 400 oC in order to confirm that no hydride phases were formed during reduction. The magnetization and coercivity showed similar variations with annealing temperature to those for the reduced powders confirming that these variations may be due to change in crystal structure rather than formation of hydrides. X-ray Diffraction (XRD) studies were performed to identify the changes in crystal phases.


2005 ◽  
Vol 20 (9) ◽  
pp. 2480-2485 ◽  
Author(s):  
Kohei Kadono ◽  
Tatsuya Suetsugu ◽  
Takeshi Ohtani ◽  
Toshihiko Einishi ◽  
Takashi Tarumi ◽  
...  

Copper(I) chloride and bromide nanoparticle-dispersed glasses were prepared by means of a conventional copper staining. The staining was performed by the following process: copper stain was applied on the surfaces of Cl−- or Br−-ion-containing borosilicate glasses, and the glasses were heat-treated at 510 °C for various times. Typical exciton bands observed in the absorption spectra of the glasses after the heat treatment indicated that CuCl and CuBr particles were formed in the surface region of the glasses. The average sizes of the CuCl and CuBr particles in the glasses heat-treated for 48 h were estimated at 4.8 and 2.7 nm, respectively. The nanoparticles were also characterized by x-ray diffraction and transmission electron microscopy. Depth profiles of Cu and CuBr concentration in the glass heat-treated for 48 h were measured. Copper decreased in concentration monotonously with depth, reaching up to 60 μm, while the CuBr concentration had a maximum at about 25 μm in depth.


1962 ◽  
Vol 6 ◽  
pp. 74-84
Author(s):  
John V. Gilfrich

AbstractX-ray diffraction studies were made on the Ti–Ni system around the stoichiometric composition of the intermetallic compound TiNi to clarify some confusion which has existed about the phase diagram in this region, and to explain some anomalies in the physical properties of this material. Wrought and cast samples were examined at room temperature both before and after heat treatment and at temperatures both above and below ambient. The compound TiNi does exist at room temperature. The phase purity of the particular sample was found to be greatly affected by such factors as minor variations in composition, heat treatment, and method of sample preparation. Some confirming metallographlc and physical property data will also be presented.


2008 ◽  
Vol 23 (4) ◽  
pp. 1020-1025 ◽  
Author(s):  
Young-Sam Jeon ◽  
Hyunho Shin ◽  
Young-Hyun Lee ◽  
Sang-Won Kang

A post heat treatment of reaction-sintered SiC at 1700 °C in nitrogen atmosphere significantly reduced electrical resistivity. A trace of insulating Si3N4 phase was detected via nitrogen heat treatment in high-resolution transmission electron microscopy observation; however, based on x-ray photoelectron spectroscopy, the evidence of nitrogen doping into SiC lattice has been claimed as the mechanism to the decreased resistivity. The increase of the total volume of SiC was apparent in x-ray diffraction during the nitrogen heat treatment, which was interpreted to stem from the growth of the nitrogen-doped intergranular SiC particles and surface doping of the primary SiC to reduce the contact resistance between the primary SiC particles.


Sensors ◽  
2019 ◽  
Vol 19 (20) ◽  
pp. 4481 ◽  
Author(s):  
Izabela Constantinoiu ◽  
Cristian Viespe

Regarding the use of hydrogen as a fuel, it is necessary to measure its concentration in air at room temperature. In this paper, sensitive composite films have been developed for surface acoustic wave (SAW) sensors, using quantum dots (QDs) and polymers. Si/SiO2 QDs were used due to having a high specific surface area, which considerably improves the sensitivity of the sensors compared to those that only have a polymer. Si/SiO2 QDs were obtained by laser ablation and analyzed by X-ray diffraction and transmission electron microscopy (TEM). Two types of polymers were used: polydimethylsiloxane (PDMS) and polymethylmethacrylate (PMMA). Polymer and polymer with QDs compositions were deposited on the sensor substrate by drop casting. A heat treatment was performed on the films at 80 °C with a thermal dwell of two hours. The sensors obtained were tested at different hydrogen concentrations at room temperature. A limit of detection (LOD) of 452 ppm was obtained by the sensor with PDMS and Si/SiO2 QDs, which was heat treated. The results demonstrated the potential of using QDs to improve the sensitivity of the SAW sensors and to achieve a heat treatment that increases its adsorption capacity of the gas molecules.


Sign in / Sign up

Export Citation Format

Share Document