US3804665A - Vapour deposition coating process - Google Patents

Vapour deposition coating process Download PDF

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US3804665A
US3804665A US24565572A US3804665A US 3804665 A US3804665 A US 3804665A US 24565572 A US24565572 A US 24565572A US 3804665 A US3804665 A US 3804665A
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chromium
process according
halide
alloy
employed
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R Chapman
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C10/00—Solid state diffusion of only metal elements or silicon into metallic material surfaces
    • C23C10/28—Solid state diffusion of only metal elements or silicon into metallic material surfaces using solids, e.g. powders, pastes
    • C23C10/30—Solid state diffusion of only metal elements or silicon into metallic material surfaces using solids, e.g. powders, pastes using a layer of powder or paste on the surface
    • C23C10/32—Chromising
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C10/00—Solid state diffusion of only metal elements or silicon into metallic material surfaces
    • C23C10/04—Diffusion into selected surface areas, e.g. using masks
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T50/00—Aeronautics or air transport
    • Y02T50/60—Efficient propulsion technologies, e.g. for aircraft
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31652—Of asbestos
    • Y10T428/31656—With metal layer

Definitions

  • ABSTRACT Metal substrates may be chromised by subjecting them to a diffusion heat treatment in which the substrate is placed in contact with a flexible carrier sheet having adherent thereto or incorporated therein chromium metal or an alloy thereof or a reducible compound of chromium.
  • a flexible carrier sheet having adherent thereto or incorporated therein chromium metal or an alloy thereof or a reducible compound of chromium.
  • Particularly suitable flexible carrier sheets are made from asbestos paper. If chromium metal or an alloy thereof is employed it is necessary that a halide is also present. This may be present either on the surface of the substrate itself, on the flexible carrier sheet bearing the chromium or its alloy or on a separate sheet of flexible carrier material.
  • the present invention relates to diffusion coatings wherein a chromium containing layer is formed on a metal substrate.
  • Such coatings are formed by the thermal decomposition of a chromium compound on the substrate, the displacement of chromium by iron from its halides at the surface of the substrate or by the reduction of a chromium compound to chromium metal at the surface of the substrate followed by diffusion of the chromium so deposited on the surface into the substrate to form what is in effect a stainless steel surface coating on it.
  • the methods of accomplishing the formation of chromium/iron difiusion layers on ferrous metal work pieces are varied.
  • One method introduces into a heated furnace containing the ferrous metal work piece, chromous halide vapour where upon reaction between the surface of the work piece and the vapour takes place.
  • Another method is to pack the work piece in a powder mixture containing a source of chromium and the container is then heated. The ingredients of the mixture interact to yield chromous halide which then reacts with the surface of the work piece.
  • Yet another method involves compacting on the surface of the ferrous substrate, a chromium-containing source which is allowed to react at temperature with the halide which is introduced into the furnace. The resulting products then react with the ferrous work piece.
  • a further method similar to the last uses an adhesive to bind the chromium to the substrate rather than compaction of the powder on to it. I
  • the essence of the present invention which mitigates these disadvantages, is to apply to a flexible carrier sheet, such as an asbestos sheet or paper or a plastic sheet either chromium metal or an alloy thereof or a compound of chromium capable of depositing the element on the substrate by thermal decomposition or by reduction and to put this coated sheet into contact with the substrate for a heat treatment.
  • a halide will also need to be present and this can be applied either to the substrate or to the carrier sheet bearing the chromium or to a separate carrier sheet before the necessary heating is carried out, so that this can react with the element to produce its halide which actually participates in the displacement reaction.
  • the present invention provides a process for producing a diffusion coating of chromium on a metal substrate, which comprises l Placing in contact with at least part of the surface of the substrate a flexible carrier sheet which has adhering to it or incorporated in it particles of chromium metal or an alloy thereof or a reducible compound of chromium, when chromium metal or an alloy thereof is present there also being present in the assembly a halide capable of reacting with the chromium and (2) subjecting such an assembly to a heat treatment to cause chromium to diffuse into the substrate.
  • Metal substrates which may be chromised to the present invention are normally ferrous. We have found that the technique may be particularly useful for chromising ferrous metal articles or sheets having a low free carbon content as these are particularly liable to the sintering problem which is mitigated by this technique.
  • a low free carbon content substrate is one which has been decarburised or has its carbon bound by a carbide-forming element such as titanium stabalised steels. Such steels normally have a free carbon content of no more than 0.02 percent frequently less than 0.01 percent.
  • the flexible carrier sheet should desirably not produce any harmful products which are likely to interefere with the production of the desired coating. If it does so, however, it is desireable that any decomposition occurring should take place at a low temperature so that the products can be purged from the furnace before any harmful effects can occur.
  • Suitable carrier sheets include sheets of cellulosic paper especially those sheets such as air mail paper, woven fabrics for example of cotton or wool, plastic fibres such as polyvinyl chloride, or polyethylene, or woven or knitted fabrics made from synthetic materials such as nylon, polyesters or acrylics. Most preferred, however, is asbestos paper. This paper may be from 2 to 10 thou thick, although we have found it is most preferable to use paper of 6 7 thou thickness.
  • the chromium or alloy thereof or reducible compound of the chromium can be applied to the flexible sheet in any convenient manner.
  • elemental powders can be compacted onto the sheet by applying them in loose powder form and then passing the material through a roller or by electroless plating or plasma spraying.
  • the sheet may be pretreated with a binder which will not give rise to appreciable amounts of harmful products which may interfere with the coating process such as ethyl silicate or polyvinyl pyrrolidone and the element applied to this.
  • a halide is required to be present as well as chromium metal or an alloy thereof, we have found that this halide may be employed as the binder.
  • halide is applied to the sheet from solution and the chromium containing metal powder then sprinkled onto the sheet while it is still wet and the whole is subsequently dried.
  • a suitable sheet can be prepared from a pulp containing asbestos, cellulosic fillers and other binders and chromium by normal paper making techniques. In such a sheet the chromium or chromium containing metal is impregnated into the material itself.
  • the present invention provides a process for forming asbestos paper sheets suitable for use in chromising as previously described, which comprises incorporating chromium metal or a chromium alloy powder as previously described, in a pulp suitable for the manufacture of asbestos paper prior to production of the paper. It also provides coated asbestos sheets produced by such a process.
  • this sandwich may be desirable to preform this sandwich, possibly using a binder to secure both sheets to each other and to the chromium or alloy powder.
  • a binder to secure both sheets to each other and to the chromium or alloy powder.
  • this can if soluble in a suitable solvent be applied from it and then dried.
  • Other methods such as roller coating or spraying may be employed if desired, however.
  • Suitable sources of chromium metal include pure chromium and alloys thereof such as ferrochrome.
  • Ferrochromes which may be employed include both the conventional material containing 5070 percent chromium and the more recently developed materials containing from 75-90 percent chromium. They may also contain other elements, such as aluminium, silicon, titanium, molybdenum, niobium, tantalum, vanadium which it may be desired to have present in the chromium diffusion alloy for various purposes, for example to combine with freed carbon from the paper to prevent it from being incorporated in the coating, to produce specific effects such as abrasion resistance or high temperature oxidation resistance in the diffusion layer.
  • Such additional elements if present will normally be present in amounts of from 2-20 percent preferably 5-10 percent by weight of the chromium.
  • the additional elements may be present either as a separate powder or as a suitable alloy with the chromium, iron or any of the other named elements.
  • the paper should be coated with a reducible halide, such as chromic chloride.
  • a reducible halide such as chromic chloride.
  • the reduction may be carried out by hydrogen gas, if the sheets used are permeable to hydrogen, or by the use of the reducing agents which do not form products to interfere with the diffusion process.
  • chromium or compound employed will depend upon the thickness of the desired coating. The best amount for a given application can be fairly readily determind by simple experimentation and we have found that for chromium metal or ferrochrome alloys amounts of about 40 g of chromium per square foot of flexible carrier are suitable. However, it may be that less amounts are suitable for particular circumstances.
  • chromium metal or an alloy is applied to the sheet it is necessary that a halide also be present.
  • This halide can be applied either to the substrate or to the carrier sheet bearing the metal or to a separate sheet which is also interposed between or wrapped around surfaces of the substrate.
  • Suitable halides are those which will react with the element at a reasonable temperature and we have found that ferrous halides such as ferrous chloride are normally particularly suitable.
  • halides such as magnesium, aluminium, nickel and manganese halides
  • cryolite and in particular the alkali metal halides such as sodium and potassium chlorides and fluorides can also be employed if desired, however some of these although satisfactory in the process are hydroscopic and pick up water from the atmosphere thus rendering the storage of the treated asbestos paper difficult.
  • oxy halides such as magnesium oxy chloride as these facilitate the storage and transportation of treated asbestos paper in normal ambient humidity without the use of any special precautions.
  • such halides also leave a residual inert harmless oxide which assists in mitigating problems which may occur as a result of sintering together of the chromium containing particles.
  • the halides can be applied simply by passing either the substrate or the flexible sheet through a solution of the halides and then drying it or as in the case of the oxy chloride by applying the dry powder to the flexible sheet with the chrome source or incorporating it in the asbestos pulp prior to the paper making.
  • the wet halide layer can act as a binder for subsequently applied chromium containing powder. It will normally be possible to employ considerably less halide than is required to react with all of the element employed, roughly 2-10 percent preferably about 5 percent of that required will normally be suitable although lesser amounts may be used if desired.
  • the solution used to apply the halide is not so acid as to result in attack on the sheet substrate. We have found that this may occur if the halide employed is aluminium chloride. In such cases satisfactory solutions can be obtained by incorporating sufficient basic material which does not iself affect the chromizing reaction to raise the pH to more than 1.2. We have found the addition of magnesium carbonate a suitable method for this purpose and that solutions of aluminium chloride containing it having a pH in that range l.2-2.5 preferably from 1.7-2.3 are particularly suitable.
  • Chromium or reducible chromium compoundbearing flexible sheets may be employed as the source of chromium deposited on the substrate during heat treatment either being wrapped around the substrate or by being interposed between adjacent surfaces thereof, for example in a stack or in a close coil. In the latter case the flexible sheet will be fed into the coil as it is being formed. It is normally desirable that they should be interposed between adjacent surfaces since this cuts down a wastage. However, if complex shaped articles are to be treated it is possible simply to wrap the sheet around them. We have also found, when the sheet employed is porous that it may be advantageous to employ a sandwich of chromium between two sheets for the heat treatment.
  • the substrate having its element or reducible compound-coated sheet in contact with it will be subjected to a heat treatment in a furnace.
  • a heat treatment in a furnace.
  • nace for example at a temperature of 400C before raising it to the operating temperature which is normally, when using chromium metal or a ferrochrome as the chromium source between 800C and 1,000C, preferably. at least 920C since the process of the invention is liable to produce unsatisfactory products if any impurity is present.
  • the process is carried outin a pure hydrogen atmosphere butargon may also be used.
  • EXAMPLE 1 0.007. in thick asbestos paper was coated on oneside with an .alloy powder containing 80% Cr and 20% Fe was then passed between the rolls of the 2 high compaction mill to compact the powder on to the paper.
  • the panels On removal from the furnace, the panelswere separated from the pack the excess powder brushed from their surfaces and then .washed.
  • the panels were attractivein appearanceand on being exposed to saltfog and to 100 percent humidity,displayed excellent corrosion resistance.
  • the mild steel substrate On cutting up one of the panels and boiling the pieces in 3 0 percentnitric' acid solution, the mild steel substrate dissolved leaving that part of the chromised panel which contained more than 13% Cr.
  • the chromised coatings were 0.002 inch thick and subsequent analysis showed them to contain an average of 25.3% Cr 74.5% Fe and 0.15% C.
  • EXAMPLE 2 A pieee of 20 gauge steel strip (0.05% C) was degreased in a solvent degreasing bath, pickled in percent v/v nitric acid for 30 seconds, and washedwith water. A solution was applied to the strip, consisting of ferrous chloride tetrahydrate (1 part) and .water (1 part), and the strip was dried under an infra-red heater to give a pick up of .4 grammes/sq.ft. of steel.
  • a stack of such sheets was constructed, each sheet being interleaved with .twolayers of 0.015 inch thick e at a rate of 40g ofpowder per sq.ft. of paper.
  • the paper asbestos sheet which had been impregnated with 18 gms/sq. ft of 83 percent chromium ferrochromium powder (200 BS mesh) during manufacture, giving a total ferrochromium concentration of 36gm/sq. ft. of steel.
  • the sheets were held between tightly bolted steel plates and placed in a suitable furnace. After purging for 16 hours at 400C in flowing hydrogen, the gas flow was stopped and the temperature was raised to 950C over a period of 8 hours and held at that temperature for a further 16 hours. After cooling the sheets were removed from the furnace and washed with water to re move excess halide.
  • the surfaces of the sheets were silver grey in colour and metallographic examination of a section of a sheet showed a chromised coating had formed of thickness 0.002 inch. A portion of the coating was separated by treatment in boilding 40 percent aqueous nitric acid. Analysis of the coating after dissolution in hydrochloric acid showed a chromium content of 22.5 percent.
  • EXAMPLE 3 Pieces of 20 gauge steel strip (0.05% C) was degreased in a solvent degreasing bath, pickled in 10 percent v/v NH3 for 30 seconds and washed with water. A paste was made consisting of magnesium chloride hexahydrate (1 part), lightly calcined Magnesium oxide (1 part) and water 1 part). To this was added 6 parts of 83 percent chromium ferrochromium powder (200 BS mesh). The mixture was spread evenly onto both sides of a sheet of asbestos paper, 0.009 inch thick, and dried in an oven held at C, to give a pick-up of 15 gms/sqft. of ferrochromium on each side of the asbestos sheet.
  • a stack was constructed consisting of alternate sheets of 20 gauge steel and coated asbestos, prepared .as described. The stack was held between tightly bolted steel plates and placed in a suitable furnace. After purging in flowing hydrogen for 16 hours at 250C the gas flow was stopped and the temperature was raised to 950C over a period of 10 hours and held at that temperature for a further 16 hours.
  • a process for producing a diffusion coating of chromium on a ferrousmetal substrate which comprises (1) placing in contact with at least part of the surface of the substrate a flexible carrier sheet containing particles of a chromium source material selected from the group consisting of chromium metal, an alloy thereof, and a reducible compound of chromium, where if said chromium source material is chromium or an alloy thereof, a halide capable of reacting with the chromium metal or alloy thereof is also present, said chromium source material being the source of the chromium in said diffusion coating of chromium on said ferrous metal substrate; and (2) subjecting said carrier sheet in contact with said substrate to a heat treatment to cause chromium to diffuse into the substrate.
  • a chromium source material selected from the group consisting of chromium metal, an alloy thereof, and a reducible compound of chromium
  • a process according to claim 1 wherein the flexible carrier sheet is plastic sheet 3.
  • said chromium source material is an iron chromium alloy; and wherein said flexible carrier sheet is selected from the group consisting of asbestos sheet or paper, cellulosic paper, and plastic sheet.
  • said flexible carrier sheet contains (i) chromium metal or an iron-chromium alloy, and (ii) said halide.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Paper (AREA)
  • Laminated Bodies (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)
US24565572 1971-04-21 1972-04-19 Vapour deposition coating process Expired - Lifetime US3804665A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1034871A GB1395703A (en) 1971-04-21 1971-04-21 Diffusion coating process

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US3804665A true US3804665A (en) 1974-04-16

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US24565572 Expired - Lifetime US3804665A (en) 1971-04-21 1972-04-19 Vapour deposition coating process

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US (1) US3804665A (OSRAM)
BE (1) BE782460A (OSRAM)
DE (1) DE2219359A1 (OSRAM)
FR (1) FR2133949A1 (OSRAM)
GB (1) GB1395703A (OSRAM)
IT (1) IT954722B (OSRAM)
NL (1) NL7205405A (OSRAM)
SE (1) SE379058B (OSRAM)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1256635A1 (en) * 2001-05-08 2002-11-13 General Electric Company Method for applying diffusion aluminide coating on a selective area of a turbine engine component
EP1528117A1 (en) * 2003-10-31 2005-05-04 General Electric Company Diffusion coating process
US7781679B1 (en) * 2005-09-09 2010-08-24 Magnecomp Corporation Disk drive suspension via formation using a tie layer and product

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2206898B (en) * 1987-07-01 1991-07-31 Electric Power Res Inst Chromized coatings containing vanadium

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1312716A (en) * 1919-08-12 Process fob coating metals
US3356528A (en) * 1962-11-15 1967-12-05 Colvilles Ltd Method and apparatus for diffusion coating of metals in coiled strips
US3585068A (en) * 1966-06-07 1971-06-15 Albright & Wilson Chromising of ferrous metal substrates
US3619232A (en) * 1968-03-29 1971-11-09 Tadashi Nakano Method of forming a pinhole-free alloy layer on the surface of a base made of aluminum or an aluminum alloy

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1312716A (en) * 1919-08-12 Process fob coating metals
US3356528A (en) * 1962-11-15 1967-12-05 Colvilles Ltd Method and apparatus for diffusion coating of metals in coiled strips
US3585068A (en) * 1966-06-07 1971-06-15 Albright & Wilson Chromising of ferrous metal substrates
US3619232A (en) * 1968-03-29 1971-11-09 Tadashi Nakano Method of forming a pinhole-free alloy layer on the surface of a base made of aluminum or an aluminum alloy

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1256635A1 (en) * 2001-05-08 2002-11-13 General Electric Company Method for applying diffusion aluminide coating on a selective area of a turbine engine component
EP1528117A1 (en) * 2003-10-31 2005-05-04 General Electric Company Diffusion coating process
US20050095358A1 (en) * 2003-10-31 2005-05-05 General Electric Company Diffusion coating process
US7390534B2 (en) 2003-10-31 2008-06-24 General Electric Company Diffusion coating process
US7781679B1 (en) * 2005-09-09 2010-08-24 Magnecomp Corporation Disk drive suspension via formation using a tie layer and product
US20100230144A1 (en) * 2005-09-09 2010-09-16 Magnecomp Corporation Disk drive suspension via formation using a tie layer and product

Also Published As

Publication number Publication date
IT954722B (it) 1973-09-15
BE782460A (fr) 1972-08-16
SE379058B (OSRAM) 1975-09-22
FR2133949A1 (OSRAM) 1972-12-01
GB1395703A (en) 1975-05-29
NL7205405A (OSRAM) 1972-10-24
DE2219359A1 (de) 1972-12-14

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