US3518106A - Process for controlled sub-micron dispersions in alloys - Google Patents

Process for controlled sub-micron dispersions in alloys Download PDF

Info

Publication number
US3518106A
US3518106A US590102A US3518106DA US3518106A US 3518106 A US3518106 A US 3518106A US 590102 A US590102 A US 590102A US 3518106D A US3518106D A US 3518106DA US 3518106 A US3518106 A US 3518106A
Authority
US
United States
Prior art keywords
alloys
dispersions
particles
micron
metal
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US590102A
Inventor
John A Alexander
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
US Department of Army
Original Assignee
US Department of Army
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by US Department of Army filed Critical US Department of Army
Application granted granted Critical
Publication of US3518106A publication Critical patent/US3518106A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals

Definitions

  • This invention relates to the controlled dispersion of dissimilar metal particles in a matrix metal in such a manner as to substantially improve the structural properties of the resultant alloy.
  • techniques for accomplishing dispersions of particles in a metal matrix include precipitation at a low temperature from a super-saturated solid solution, by eutectoid decomposition and by mechanical mixing of powders.
  • the first two of these techniques are diffusion processes and thus the size and distribution of particles is subject to change during elevated temperature exposure. Dissolution or agglomeration of particles by diffusion is detrimental to the elevated temperature properties of these types of alloys.
  • the third process incorporates stable particles in the metal matrix by mechanical mixing.
  • SAP dispersion alloys are formed by pressing metal powders such as aluminum which have been surface oxidized.
  • TD type dispersion alloys typically involve the colloidal codispersion of thorium OXide and nickel oxide followed by the reduction of the nickel oxide.
  • This objective is achieved by the treatment of this process which consists in depositing a thin film of the intended matrix metal of controlled thickness by vacuum deposition; subsequently a dissimilar metal which can be preferentially oxidized is vacuum deposited in a quantity sufficient to initiate the formation of isolated islands on the thin film substrate; the island deposit can be characterized as having an average island diameter and an inter-island distance or spacing; the island diameter and the inter-island distance can be controlled by variations in the substrate temperature, the rate of deposition and the time of deposition.
  • the planner dispensersion created in this manner is preferentially oxidized by simple exposure to oxygen at elevated temperature or by anodization techniques.
  • the oxidized planar dispersion is then overlayed by a second layer of the matrix metal of equal thickness and this dispersion of the intermediate layer provides a thermodynamically stable second phase.
  • the treatment heretofore outlined is repeated and this results in the construction of a three dimensional distribution of dispersed second phase particles in the matrix metal. This treatment permits complete control over the particle size in the submicron range and over interparticle spacing on the same sub-micron scale.
  • the process was carried out by depositing aluminum islands on a gold substrate with the aluminum being oxidized to aluminum oxide.
  • This process is also applicable to the formation of stable oxide, carbide, nitride, boride, phosphide or silicide particles in structural metals such as nickel, chromium, cobalt, titanium, columbium, tantalum, molybdenum, tungsten, aluminum, magnesium, iron and copper.
  • the drawing is a schematic illustration of strength versus temperature curve for a conventional metallic alloy as compared with a dispersion strengthened alloy.
  • the dispersion strengthened materials are advantageous for the design of equipment for elevated temperature because their strengths are maintained relatively constant over a broad temperature range as indicated in the drawing.
  • the shaded area indicates the temperature range over which a dispersion strengthened alloy can be expected to excel in design for the elevated temperature application.
  • a process for the production of sub-micron size dispersions in metals or alloys comprising, depositing in a vacuum on a heated matrix metal a. dissimilar metal from a vapor for the formation of closely spaced sub-micron size islands, oxidizing the metal islands for the formation of a planar dispersion of particles, overlaying the oxidized planar dispersion with a layer of the matrix metal, and repeating these steps to form a three dimensional alloy structure of matrix metal with oxidized dispersions of submicron particles of a dissimilar metal distributed therethrough, said alloy structure having high structural strength suitable for sustained use in high temperature applications.

Description

June 30, 1970 J.'A.'ALEXANDER 3,513,
PROCESS FOR CONTROLLED SUB-MICRON DISPERSIONS IN ALLOYS Filed 001;; 27, 1966 dire/191 7 7mperazure Comparisop of .Sfrengf/z vs. fempe/aure for disperszorz strengthened and h0m09enou5 afloys INVENTOR, Jbhn QQ/exanaer BY 22/ /1414 w Maul ATTORNEYS.
United States Patent Oflice 3,518,106 Patented June 30, 1970 3,518,106 PROCESS FOR CONTROLLED SUB-MICRON DISPERSIONS IN ALLOYS John A. Alexander, Oxon Hill, Md., assignor to the United States of America as represented by the Secretary of the Army Filed Oct. 27, 1966, Ser. No. 590,102 Int. Cl. 844d 1/14 US. Cl. 117-71 2 Claims ABSTRACT OF THE DISCLOSURE An alloy having high structural strength suitable for use in such high temperature applications as gas turbine equipment, which is produced by vacuum deposition of dispersions of sub-micron particles of a dissimilar metal on a thin heated layer of a matrix metal, oxidation of the dispersions of particles, overlaying the oxidized 'dispersions with a second thin layer of the matrix metal, and repeating the process of depositing dispersions of submicron particles oxidized and covered with a layer of matrix metal to produce a three dimensional alloy structure of matrix metal with dispersions of sub-micron particles of a dissimilar metal distributed in the matrix metal.
The invention described herein may be manufactured and used by or for the Government, for governmental purposes, without the payment to me of any royalty thereon.
This invention relates to the controlled dispersion of dissimilar metal particles in a matrix metal in such a manner as to substantially improve the structural properties of the resultant alloy.
Heretofore, techniques for accomplishing dispersions of particles in a metal matrix include precipitation at a low temperature from a super-saturated solid solution, by eutectoid decomposition and by mechanical mixing of powders. The first two of these techniques are diffusion processes and thus the size and distribution of particles is subject to change during elevated temperature exposure. Dissolution or agglomeration of particles by diffusion is detrimental to the elevated temperature properties of these types of alloys. The third process incorporates stable particles in the metal matrix by mechanical mixing. The
size and uniformity of spacing of such mixtures is dependent upon availability of micron size particles and the ability of the fabricator to accomplish homogeneous mixtures. At least two techniques for the accomplishment of more controlled particle size and distribution exist in the SAP and TD type powders. SAP dispersion alloys are formed by pressing metal powders such as aluminum which have been surface oxidized. TD type dispersion alloys typically involve the colloidal codispersion of thorium OXide and nickel oxide followed by the reduction of the nickel oxide.
Each of the above described state of the art processes are limited by elevated temperature instability, relatively coarse particle size, non-uniform distribution or relatively large interparticle spacing.
It is therefore the object of this invention to overcome these disadvantages by attaining a uniform dispersion of a very fine temperature stable phase in the desired matrix with small interparticle spacing.
This objective is achieved by the treatment of this process which consists in depositing a thin film of the intended matrix metal of controlled thickness by vacuum deposition; subsequently a dissimilar metal which can be preferentially oxidized is vacuum deposited in a quantity sufficient to initiate the formation of isolated islands on the thin film substrate; the island deposit can be characterized as having an average island diameter and an inter-island distance or spacing; the island diameter and the inter-island distance can be controlled by variations in the substrate temperature, the rate of deposition and the time of deposition. The planner :dispersion created in this manner is preferentially oxidized by simple exposure to oxygen at elevated temperature or by anodization techniques. The oxidized planar dispersion is then overlayed by a second layer of the matrix metal of equal thickness and this dispersion of the intermediate layer provides a thermodynamically stable second phase. The treatment heretofore outlined is repeated and this results in the construction of a three dimensional distribution of dispersed second phase particles in the matrix metal. This treatment permits complete control over the particle size in the submicron range and over interparticle spacing on the same sub-micron scale.
Experimentally the process was carried out by depositing aluminum islands on a gold substrate with the aluminum being oxidized to aluminum oxide. This process is also applicable to the formation of stable oxide, carbide, nitride, boride, phosphide or silicide particles in structural metals such as nickel, chromium, cobalt, titanium, columbium, tantalum, molybdenum, tungsten, aluminum, magnesium, iron and copper.
The drawing is a schematic illustration of strength versus temperature curve for a conventional metallic alloy as compared with a dispersion strengthened alloy. The dispersion strengthened materials are advantageous for the design of equipment for elevated temperature because their strengths are maintained relatively constant over a broad temperature range as indicated in the drawing. The shaded area indicates the temperature range over which a dispersion strengthened alloy can be expected to excel in design for the elevated temperature application.
There are many advantages in having such materials available for more severe temperature environments and as a practical application this improvement becomes particularly important in the increased efliciencies which re sult from being able to design and operate gas turbine equipment at higher temperatures.
Thus, the essence of this treatment for the formation of alloys, is that it alfords a means of controlling the size of the islands and their spacing which is utilized to miniaturize these dimensions for improvement in the structural qualities of the laminated product.
What is claimed is:
1. A process for the production of sub-micron size dispersions in metals or alloys comprising, depositing in a vacuum on a heated matrix metal a. dissimilar metal from a vapor for the formation of closely spaced sub-micron size islands, oxidizing the metal islands for the formation of a planar dispersion of particles, overlaying the oxidized planar dispersion with a layer of the matrix metal, and repeating these steps to form a three dimensional alloy structure of matrix metal with oxidized dispersions of submicron particles of a dissimilar metal distributed therethrough, said alloy structure having high structural strength suitable for sustained use in high temperature applications.
2. The process of claim 1 in which the matrix layers comprise films of gold and the islands comprise aluminum which is oxidized to form aluminum oxide.
References Cited UNITED STATES PATENTS 3,261,720 7/1966 McCormack 117-107 X 3,368,919 2/1968 Casale et all. 117-212 X ALFRED L. LEAVITT, Primary Examiner C. K. WEIFFENBACH, Assistant Examiner U.S. Cl. X.R. 117-107
US590102A 1966-10-27 1966-10-27 Process for controlled sub-micron dispersions in alloys Expired - Lifetime US3518106A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US59010266A 1966-10-27 1966-10-27

Publications (1)

Publication Number Publication Date
US3518106A true US3518106A (en) 1970-06-30

Family

ID=24360883

Family Applications (1)

Application Number Title Priority Date Filing Date
US590102A Expired - Lifetime US3518106A (en) 1966-10-27 1966-10-27 Process for controlled sub-micron dispersions in alloys

Country Status (1)

Country Link
US (1) US3518106A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3261720A (en) * 1961-10-11 1966-07-19 Nat Starch Chem Corp Thermoelectric generator and method of preparing same
US3368919A (en) * 1964-07-29 1968-02-13 Sylvania Electric Prod Composite protective coat for thin film devices

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3261720A (en) * 1961-10-11 1966-07-19 Nat Starch Chem Corp Thermoelectric generator and method of preparing same
US3368919A (en) * 1964-07-29 1968-02-13 Sylvania Electric Prod Composite protective coat for thin film devices

Similar Documents

Publication Publication Date Title
Koch Structural nanocrystalline materials: an overview
WO2018144324A4 (en) Additive manufacturing with nanofunctionalized precursors
US20150368535A1 (en) Graphene composites and methods of fabrication
JP7198211B2 (en) Sputter target and method for manufacturing sputter target
US3711279A (en) Methods for manufacture of sintering thin porous metallic sheets
US3714702A (en) Method for diffusion bonding refractory metals and alloys
JPS58171502A (en) Pulverized composite powder of ceramic and metal
Steiner et al. Core level binding energy shifts in Ni on Au and Au on Ni overlayers
JP2017502166A (en) Sputtering target and manufacturing method thereof
US3518106A (en) Process for controlled sub-micron dispersions in alloys
US3197847A (en) Clad materials and process of fabricating the same
US3113376A (en) Alloying
Grigoreva et al. Mechanochemical synthesis of Cu–Al alloyed powders and their consolidation by spark plasma sintering
US3270412A (en) Method of producing dispersoid strengthened material
US5849373A (en) Process for the synthesis of nanophase dispersion-strengthened aluminum alloy
Mukherjee et al. Temperature-induced chaos during nanorod growth by physical vapor deposition
KR20200019387A (en) Method for manufacturing dispersion-strengthened metal sintered body
US6908691B2 (en) Metal strip for epitaxial coatings and method for the production thereof
US3692596A (en) Dispersion strengthened nickel-chromium alloys
Poniatowski et al. Dispersion hardened gold: A new material of improved strength at high temperatures
Kedward et al. ELECTRODEPOSITED COMPOSITE COATINGS FOR WEAR RESISTANCE.
CN111041414A (en) Method for preparing metal nanosheet and metal nanosheet
US3694270A (en) Hard superconductive materials and method of producing the same
US3577227A (en) Tungsten materials and a method for providing such materials
JP2695099B2 (en) Metal coating method for inorganic fine powder surface