Hydrogenizing Effect of Steam on Ferrous Alloys at Elevated Temperatures

2009 ◽  
pp. 50-50-9
Author(s):  
C. A. Zapffe ◽  
F. K. Landgraf
Keyword(s):  
Elevated Temperatures ◽  
Ferrous Alloys

scholarly journals Development of Creep-Resistant, Alumina-Forming Ferrous Alloys for High-Temperature Structural Use

2018 ◽  
Author(s):  
Y. Yamamoto ◽  
M. P. Brady ◽  
G. Muralidharan ◽  
B. A. Pint ◽  
P. J. Maziasz ◽  
...  
Keyword(s):  
High Temperature ◽  
Elevated Temperatures ◽  
Extreme Environments ◽  
Alloy Design ◽  
Austenitic Steels ◽  
Strength Development ◽  
Second Phase ◽  
Ferrous Alloys ◽  
Steel Alloys ◽  
Structural Applications

This paper overviews recent advances in developing novel alloy design concepts of creep-resistant, alumina-forming Fe-base alloys, including both ferritic and austenitic steels, for high-temperature structural applications in fossil-fired power generation systems. Protective, external alumina-scales offer improved oxidation resistance compared to chromia-scales in steam-containing environments at elevated temperatures. Alloy design utilizes computational thermodynamic tools with compositional guidelines based on experimental results accumulated in the last decade, along with design and control of the second-phase precipitates to maximize high-temperature strengths. The alloys developed to date, including ferritic (Fe-Cr-Al-Nb-W base) and austenitic (Fe-Cr-Ni-Al-Nb base) alloys, successfully incorporated the balanced properties of steam/water vapor-oxidation and/or ash-corrosion resistance and improved creep strength. Development of cast alumina-forming austenitic (AFA) stainless steel alloys is also in progress with successful improvement of higher temperature capability targeting up to ∼1100°C. Current alloy design approach and developmental efforts with guidance of computational tools were found to be beneficial for further development of the new heat resistant steel alloys for various extreme environments.

scholarly journals The Effect of Nanostructure Modification on the Silicate Binder on Its Binding Characteristics and Functional Properties

2014 ◽  
Vol 59 (3) ◽  
pp. 1033-1036 ◽  
Author(s):  
I. Izdebska-Szanda ◽  
A. Baliński ◽  
M. Angrecki ◽  
A. Palma
Keyword(s):  
Chemical Modification ◽  
Sodium Silicate ◽  
Functional Properties ◽  
Elevated Temperatures ◽  
Technological Properties ◽  
Ferrous Alloys ◽  
Silicate Binder ◽  
Binding Characteristics ◽  
The Impact

Abstract A method for the chemical modification of silicate binder (hydrated sodium silicate) affecting the distribution of its nanostructure elements was disclosed. The effect of silicate binder modification on the resulting technological properties of moulding sands, determined under standard conditions and at elevated temperatures in the range from 1000C to 9000C, was discussed. Modification of this type is done on inorganic binders in order to reduce their unfavourable functional properties. It is particularly important when moulding sands with the silicate binder are used for casting of low-melting alloys. Therefore special attention was paid to the impact that modification of inorganic binders may have on the knocking out properties of sands prepared with these binders, when they are used in the process of casting non-ferrous alloys.

Electrochemical Phase Diagrams for the Fe/S/H2O System under Geothermal Conditions

1985 ◽  
Vol 38 (5) ◽  
pp. 643 ◽  
Author(s):  
BG Pound ◽  
GA Wright ◽  
RM Sharp
Keyword(s):  
New Zealand ◽  
Phase Diagrams ◽  
Elevated Temperatures ◽  
Corrosion Products ◽  
Ferrous Alloys ◽  
Temperature Range ◽  
General Terms ◽  
Geothermal Fluids ◽  
Region Of Stability ◽  
Regions Of Stability

Previously published electrochemical phase (potential-pH) diagrams for the Fe/S/H2O system at elevated temperatures are assessed. It is concluded that the potential-pH equations derived by Biernat and Robins1 can be used to provide reliable diagrams over the temperature range 298-573 K. These equations were used to derive a set of diagrams relevant to geothermal fluids in general terms, so that the corrosion products of iron and ferrous alloys immersed in these fluids may be predicted. In addition, diagrams are presented for geothermal fluids in the Broadlands and Wairakei fields in New Zealand. The significant changes in the E-pH diagrams as the temperature increases over the range 298-573 K are that the region of stability for Fe(OH)3- widens and the regions of stability for FeS2 and Fe3O4 and, at higher temperatures, FeS, shrink in size.

Characterization of Rare-Earth Fluoride Anti-Stokes Phosphors by Scanning arid Transmission Electron Microscopy

1971 ◽  
Vol 29 ◽  
pp. 142-143
Author(s):  
N. M. P. Low ◽  
L. E. Brosselard
Keyword(s):  
Electron Microscopy ◽  
Rare Earth ◽  
Elevated Temperatures ◽  
Stoichiometric Composition ◽  
Rare Earth Ions ◽  
Crystalline Solid ◽  
Precipitation Process ◽  
Rare Earth Fluoride ◽  
Earth Fluoride ◽  
Rare Earth Fluorides

There has been considerable interest over the past several years in materials capable of converting infrared radiation to visible light by means of sequential excitation in two or more steps. Several rare-earth trifluorides (LaF3, YF3, GdF3, and LuF3) containing a small amount of other trivalent rare-earth ions (Yb3+ and Er3+, or Ho3+, or Tm3+) have been found to exhibit such phenomenon. The methods of preparation of these rare-earth fluorides in the crystalline solid form generally involve a co-precipitation process and a subsequent solid state reaction at elevated temperatures. This investigation was undertaken to examine the morphological features of both the precipitated and the thermally treated fluoride powders by both transmission and scanning electron microscopy.Rare-earth oxides of stoichiometric composition were dissolved in nitric acid and the mixed rare-earth fluoride was then coprecipitated out as fine granules by the addition of excess hydrofluoric acid. The precipitated rare-earth fluorides were washed with water, separated from the aqueous solution, and oven-dried.

Observations oh Nucleation and Growth of Voids in Nickel

1970 ◽  
Vol 28 ◽  
pp. 414-415
Author(s):  
J. L. Brimhall ◽  
H. E. Kissinger ◽  
B. Mastel
Keyword(s):  
High Purity ◽  
Growth Stage ◽  
Elevated Temperatures ◽  
Early Growth ◽  
Nucleation And Growth ◽  
Pure Nickel ◽  
Different Temperatures ◽  
Total Fluence ◽  
Neutron Exposure ◽  
Growth Of Voids

Some information on the size and density of voids that develop in several high purity metals and alloys during irradiation with neutrons at elevated temperatures has been reported as a function of irradiation parameters. An area of particular interest is the nucleation and early growth stage of voids. It is the purpose of this paper to describe the microstructure in high purity nickel after irradiation to a very low but constant neutron exposure at three different temperatures.Annealed specimens of 99-997% pure nickel in the form of foils 75μ thick were irradiated in a capsule to a total fluence of 2.2 × 1019 n/cm2 (E > 1.0 MeV). The capsule consisted of three temperature zones maintained by heaters and monitored by thermocouples at 350, 400, and 450°C, respectively. The temperature was automatically dropped to 60°C while the reactor was down.

Voids in Irradiated Tungsten and Molybdenum

1969 ◽  
Vol 27 ◽  
pp. 190-191
Author(s):  
Robert C. Rau ◽  
Robert L. Ladd
Keyword(s):  
Melting Point ◽  
Fast Neutron ◽  
Neutron Irradiation ◽  
Elevated Temperatures ◽  
Irradiation Temperature ◽  
The Body ◽  
Face Centered Cubic ◽  
Body Centered Cubic ◽  
Cubic Metals ◽  
Face Centered

Recent studies have shown the presence of voids in several face-centered cubic metals after neutron irradiation at elevated temperatures. These voids were found when the irradiation temperature was above 0.3 Tm where Tm is the absolute melting point, and were ascribed to the agglomeration of lattice vacancies resulting from fast neutron generated displacement cascades. The present paper reports the existence of similar voids in the body-centered cubic metals tungsten and molybdenum.

Mechanical Properties and Dislocation Structure of Single Crystal Cdte Deformed in Compression at 300°C

1976 ◽  
Vol 34 ◽  
pp. 592-593
Author(s):  
Ernest L. Hall ◽  
J. B. Vander Sande
Keyword(s):  
Mechanical Properties ◽  
Single Crystal ◽  
Dislocation Structure ◽  
Room Temperature ◽  
Elevated Temperatures ◽  
Strain Curve ◽  
Optical Devices ◽  
Semiconductor Compound ◽  
Wide Range ◽  
Sample Orientation

The present paper describes research on the mechanical properties and related dislocation structure of CdTe, a II-VI semiconductor compound with a wide range of uses in electrical and optical devices. At room temperature CdTe exhibits little plasticity and at the same time relatively low strength and hardness. The mechanical behavior of CdTe was examined at elevated temperatures with the goal of understanding plastic flow in this material and eventually improving the room temperature properties. Several samples of single crystal CdTe of identical size and crystallographic orientation were deformed in compression at 300°C to various levels of total strain. A resolved shear stress vs. compressive glide strain curve (Figure la) was derived from the results of the tests and the knowledge of the sample orientation.

Electron microscopy of crystalline structure in thermotropic random copolymers

1991 ◽  
Vol 49 ◽  
pp. 1054-1055
Author(s):  
Afzana Anwer ◽  
S. Eilidh Bedford ◽  
Richard J. Spontak ◽  
Alan H. Windle
Keyword(s):  
Electron Microscopy ◽  
Crystalline Structure ◽  
Liquid Crystalline ◽  
Elevated Temperatures ◽  
Random Copolymers ◽  
Molecular Characteristics ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Identical Monomer ◽  
Periodic Layer

Random copolyesters composed of wholly aromatic monomers such as p-oxybenzoate (B) and 2,6-oxynaphthoate (N) are known to exhibit liquid crystalline characteristics at elevated temperatures and over a broad composition range. Previous studies employing techniques such as X-ray diffractometry (XRD) and differential scanning calorimetry (DSC) have conclusively proven that these thermotropic copolymers can possess a significant crystalline fraction, depending on molecular characteristics and processing history, despite the fact that the copolymer chains possess random intramolecular sequencing. Consequently, the nature of the crystalline structure that develops when these materials are processed in their mesophases and subsequently annealed has recently received considerable attention. A model that has been consistent with all experimental observations involves the Non-Periodic Layer (NPL) crystallite, which occurs when identical monomer sequences enter into register between adjacent chains. The objective of this work is to employ electron microscopy to identify and characterize these crystallites.

Generation of 4H and 6H Structures During the Hexagonal-Rhombohedral Transformation in Dy2Co17

1975 ◽  
Vol 33 ◽  
pp. 38-39
Author(s):  
C. W. Allen ◽  
D. L. Kuruzar
Keyword(s):  
Elevated Temperatures ◽  
Layer Structure ◽  
Transition Element ◽  
Temperature Structure ◽  
Allotropic Transformation ◽  
Layer Plane ◽  
Planar Defects ◽  
Topologically Close Packed ◽  
Transformation Mechanisms ◽  
Shear Transformation

The rare earth/transition element intermetallics R2T17 are essentially topologically close packed phases for which layer structure models have already been presented. Many of these compounds are known to undergo allotropic transformation of the type at elevated temperatures. It is not unexpected that shear transformation mechanisms are involved in view of the layering character of the structures. The transformations are evidently quite sluggish, illustrated in furnace cooled Dy2Co17 by the fact that only rarely has the low temperature rhombohedral form been seen. The more usual structures observed so far in furnace cooled alloys include 4H and 6H in Dy2Co17 (Figs. 1 and 2) . In any event it is quite clear that the general microstructure is very complicated as a consequence of the allotropy, illustrated in Fig. 3. Numerous planar defects in the layer plane orientation are evident as are non-layer plane defects inherited from a high temperature structure.

Spherulite Structures in a Melt Spun Fe-Ni Austenitic Steel

1985 ◽  
Vol 43 ◽  
pp. 52-53
Author(s):  
G. M. Michal ◽  
T. K. Glasgow ◽  
T. J. Moore
Keyword(s):  
Austenitic Steel ◽  
Room Temperature ◽  
Elevated Temperatures ◽  
Large Range ◽  
Amorphous Structure ◽  
Nucleation And Growth ◽  
Ni Alloys ◽  
Melt Spun ◽  
Crystal Fibers ◽  
Rapidly Solidified

Large additions of B to Fe-Ni alloys can lead to the formation of an amorphous structure, if the alloy is rapidly cooled from the liquid state to room temperature. Isothermal aging of such structures at elevated temperatures causes crystallization to occur. Commonly such crystallization pro ceeds by the nucleation and growth of spherulites which are spherical crystalline bodies of radiating crystal fibers. Spherulite features were found in the present study in a rapidly solidified alloy that was fully crysstalline as-cast. This alloy was part of a program to develop an austenitic steel for elevated temperature applications by strengthening it with TiB2. The alloy contained a relatively large percentage of B, not to induce an amorphous structure, but only as a consequence of trying to obtain a large volume fracture of TiB2 in the completely processed alloy. The observation of spherulitic features in this alloy is described herein. Utilization of the large range of useful magnifications obtainable in a modern TEM, when a suitably thinned foil is available, was a key element in this analysis.

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