GB2153392A - Spray deposition of metal - Google Patents
Spray deposition of metal Download PDFInfo
- Publication number
- GB2153392A GB2153392A GB08500490A GB8500490A GB2153392A GB 2153392 A GB2153392 A GB 2153392A GB 08500490 A GB08500490 A GB 08500490A GB 8500490 A GB8500490 A GB 8500490A GB 2153392 A GB2153392 A GB 2153392A
- Authority
- GB
- United Kingdom
- Prior art keywords
- deposit
- molten
- substrate
- process according
- spray
- 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.)
- Granted
Links
- 229910052751 metal Inorganic materials 0.000 title claims description 36
- 239000002184 metal Substances 0.000 title claims description 36
- 238000009718 spray deposition Methods 0.000 title description 7
- 239000007921 spray Substances 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 24
- 230000008569 process Effects 0.000 claims description 24
- 239000000758 substrate Substances 0.000 claims description 24
- 239000002923 metal particle Substances 0.000 claims description 5
- 238000012544 monitoring process Methods 0.000 claims description 5
- 238000000151 deposition Methods 0.000 description 11
- 239000007789 gas Substances 0.000 description 11
- 239000002245 particle Substances 0.000 description 10
- 230000008021 deposition Effects 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 238000001816 cooling Methods 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 230000005855 radiation Effects 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 230000008023 solidification Effects 0.000 description 4
- 238000007711 solidification Methods 0.000 description 4
- 238000004616 Pyrometry Methods 0.000 description 3
- 239000012634 fragment Substances 0.000 description 3
- 229910000975 Carbon steel Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 235000019628 coolness Nutrition 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 229910001338 liquidmetal Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000002310 reflectometry Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
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
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
-
- 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
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
- C23C4/123—Spraying molten metal
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Coating By Spraying Or Casting (AREA)
Description
1
SPECIFICATION
Spray deposition of metal This invention relates to a process of producing a metal body by depositing sprayed particles. British Patent Specification 1262471 describes a way in which strip and sheet can be produced by directing a stream of molten gas-atomised metal particles on to a moving substrate to form a deposit which is subsequently hot worked to form the required product. A more recent research investigation (Metals Technology, February 1983, pages 61 -68) has revealed and analysed various mechanisms that can operate during the spray deposition process itself, thereby giving rise to differing structures in the deposit.
It has now been found that failure to select appropriate conditions for spray deposition for each melt or alloy may lead to poor mechanical properties even after enough hot working to ensure full densification. In such cases, further hot deformation (which is liable to cause anisotropy), and possibly intermediate annealing or sintering, may be needed to achieve otherwise good mechanical properties. These additional treatments may render the process uneconomic and unattractive. It is therefore important to arrange matters such that the conditions of spray deposition are correct, as follows.
With low spray density coupled with high rates of cooling, as explained in the Metals Technology paper, the average molten droplet of a spray lands on the preceding splat after that splat has fully solidified; thus a layered deposit is build up, each layer consisting of a splat thickness. If the spray density is higher or the rate of cooling is lower, the average molten droplet of a spray lands on the preceding splat before the top surface of that splat has solidified; thus the two liquids mix, and the deposit hence shows little evidence of layering.
Small amounts of oxygen derived from the air may have a disproportionate effect on the behaviour of the deposits during subsequent hot working, and on the mechanical proper- ties of the product. Air is difficult and expensive to exclude completely from industrial operations. Protective atmospheres rich in CO or H, will counteract the effects of oxygen on iron and many steels such as carbon steels but not on metals and alloys such as Al, Ti and chromium-steels, which have a very high affinity for oxygen. There, formation of the metallic oxides is practically inevitable and one has to minimise the harm they do.
If for example a deposit k of A[ is made at low spray density and with a high rate of substrate cooling where merely normal industrial precautions are taken to exclude air, each droplet of spray typically becomes coated with 65 a very thin, say 10-11m, skin of AI,O,, which GB 2 153 392A 1 is very strong, insoluble, tenacious yet brittle, and cannot be reduced by any gas at reasonable temperatures. In addition the preceding (solidified) splat is also covered with a similar oxide skin.
As it lands, each molten droplet breaks its oxide skin, revealing new unoxidised metal instantaneously. The surface area of the new splat (formed from the droplet) is typically 2 to 20 times as large as was the surface area of the droplet. Its brittle oxide skin is fragmented and only plays a minor part in subsequent events. The oxide skin on the fully solidified preceding splat stays intact however, and forms a continuous boundary between the new splat and the preceding splat. The subsequent deposit structure is layered, lacks coherence and has poor mechanical properties because of the presence of the intervening oxide film.
When the deposit is subsequently hot worked the brittle oxide skins are gradually broken up, but strains of say 60%-90% or long times of high temperature sintering are necessary to give good mechanical properties; such treatments are costly and may be undesirable technically.
Contamination with oxygen being industrially unavoidable as already mentioned, operating conditions must be selected so that its most deleterious effect-a thin unbroken skin of oxide as just described-is avoided. This can be accomplished for example by using a higher spray density or a lower rate of cool- ing, so that, in consequence, each average droplet now lands on the preceding splat before the top surface of that splat has fully solidified. Both the droplet and the molten top surface of the splat are covered with a very thin skin of oxide but, when the two liquid surfaces meet, the consequent turbulence breaks both these skins and disperses the fragments. The two liquids mix and on subsequent solidification give a non-layered struc- ture that has coherence and reasonable ductility because the very small fragments of oxide are no longer present as continuous skins or films but as dispersed discontinous fragments.
These measures are useful not only for aluminium, but also for such elements as Mn, Mo and W (even though their oxide skins are more easily dispersed and hence rendered relatively innocuous), and also for iron or carbon steel (where otherwise a reducing at- mosphere rather than an inert atmosphere might be necessary), and can be used for any other metal, even such as copper. In this connection, the solid solubility of an oxide in its own molten metal has an effect. When this solubility is reasonably high, dispersed oxide films are more easily -bailed-up- because of surface tension effects, Ti being outstanding in this respect (although large quantities of its oxide are still harmful). Iron oxides have a limited solid solubility in Fe but sufficient to 2 GB 2 153 392A 2 enable any oxide films to re-aggregate as discontinuous particles and so become rela tively innocuous.
According to the present invention, a pro cess of producing a metal body (e.g. strip or 70 sheet) comprises atomising a source of molten metal and directing the atomised molten metal particles (as a spray) on to a cooler substrate, on which the molten metal particles splat and build up to form a deposit, the deposit being optionally subsequently re moved from the substrate, and optionally hot worked, the process being characterised by (for example by responding to monitoring the appearance of the surface of the deposit, or by programming) controlling the spray condi tions, so that the whole, or most, of the surface of the deposit is molten throughout the process.
The purpose is to make certain that on average each molten particle lands on the preceding splat in that position while at least the top surface of that splat is still molten.
Preferably, the spray is directed so as to scan the directed stream over a desired area of the substrate such that, at every point in that area, incremental conditions are maintained, i.e. the average droplet lands on the preceding droplet on the substrate while at least the top surface of that preceding droplet is still molten but the thickness of molten metal does not increase beyond what is restrainable by the surface tension and viscosity of the molten metal. The programme to achieve this will maintain an arrival rate of metal droplets at any point commensurate with the rate of heat extraction from that point, thus allowing less metal to arrive at an already thickly coated plate (where heat will be lost slowly) and allowing more metal to arrive at a so far uncoated place (where heat will be lost quickly).
The programme may arise from closed-loop or heuristic feedback and may direct the con- trol means to alter the conditions in various ways, for example, on the next cycle to reach the point, to alter the scanning speed or the advance per line of scan.
Preferably the stream of droplets strikes the substrate at an angle.
Preferably the programme maintains the deposit at a thickness which at any given point is substantially proportional to the square root of the distance of that point from the leading edge of the deposit.
The invention also provides a process for depositing a metal on a substrate by forming a source of molten metal into a directed stream of droplets and controlling the direc- tion of the stream according to a programme as set forth above.
It will be appreciated that the deposition of molten particles from a spray is a random process in which the precise behaviour of each individual molten particle cannot be known or predicted, although the behaviour of the average particle can be clearly defined. Thus, even with the most careful control, a small proportion of the molten particles will, by chance, land on a splat which has already fully solified. Moreover atomisation itself is a random process, in which a small proportion (by weight) of the particles in a nominally molten spray will be solid by the time they land on a prior splat. This specification necessarily refers to the behaviour of the particles or splats as a whole, i.e. the behaviour of the average particle or splat.
To keep the surface of the deposit still molten, as required, at the instant that a new droplet lands on it, one or more of the spray conditions must be controlled, such as (mainly) speed and cooling rate of substrate, atomising gas flow, pressure and temperature, molten metal feed rate, spray scanning rate and temperature. Of these, the cooling rate of the substrate, temperature of atomising gas and molten metal temperature, while adjustable, cannot readily be used to correct and control short-term fluctuations in the process. Moreover atomising gas flow and pressure are usually linked by virtue of fixed nozzle dimensions. The spray conditions controlled by the process according to the invention are thus preferably the substrate speed, scanning rate, metal flow rate and gas pressure, the other conditions normally being fixed during any one run. Increasing substrate speed, increasing gas pressure and decreasing metal flow rate bring about more rapid freezing and decrease the depth of liquid on the surface of the deposit, and vice versa.
In one preferred mode of controlling the spray conditions, the appearance of the sur- face of the deposit is monitored (to check its molten-ness) and the spray conditions are controlled in response. The monitoring'of the surface of the deposit may be by direct observation of the surface where deposition is oc- curring, and can be conducted visually, directly or through tinted or smoked glass. The observation may be by video, in which case there is advantage in having a picture -freeze- for a sequence of periods of, say, 1 second at a time. The observation can be by radiation pyrometry, or by reflectivity measurements (at preset angles) of the surface.
If visual observation or video is used it will be clearly apparent when most of the prior splat surface is molten. By this is meant generally more than 80% and always more than 50%. The extent of the molten surface is shown by the fact that the molten splat surface is smooth and bright, though rippled due to impinging gases and vibrations, compared with the solidified splat surface that is matt and immobile. With the unaided eye events happen so rapidly that only a general effect will be seen but this is quite distinctive. By -freezing- for short intervals using video the 3 picture becomes clearer and a more accurate assessment can be made of the situation.
Although because of the random nature of spray deposition some areas of the surface for a brief period will always solidify, it is preferable for the whole splatted surface to be molten during deposition. However, the molten splat layer should not be allowed to become too thick, otherwise conditions will re- vert to those of conventional casting and some benefits of spray forming will be lost such as small grain size and avoidance of segregation. The fully molten layer should typically not be as thick as 1 mm, but the precise thickness which should preferably not be exceeded depends in each case on viscosity and surface tension. We can recognise whether the thickness is excessive by seeing if massive ripples, or flow involving areas far larger than one splat, occur as a result of the gases impinging on the surface or, if the substrdte is being sprayed in an attitude other than horizontal, by seeing if the molten deposited metal runs off under gravity. Preferably, the monitoring of the appearance of the surface can recognise an excessively thick molten layer and can control the spray conditions accordingly.
Under typical control, the speed of the substrate, the pressure of atomising gas and the rate of flow of liquid metal from the nozzle are altered until a molten layer covers most or all of the depositing surface. Preferably these parameters are controlled additionally such that the molten layer is not too thick.
Radiation pyrometry can be used for the monitoring. In this case, after due allowance has been made for emissivity and absorption, the monitored temperature of the surface will indicate the average depth of liquid. If the average temperature of the deposited surface is at or below the solidus the average depth of liquid is too small. If the average temperature of the deposited surface is above the liquidus, the average depth of liquid is likely to be too great. In the case of a pure metal, the temperature of the surface must remain as close as practicable to the melting point. The spray conditions are controlled accordingly.
To produce strip or sheet, the spray may be 115 scanned, that is, typically reciprocated over the width of the strip (transverse to the length, and direction of motion, of the strip). The scanning should be fast enough that the spray returns to any particular position before the top of the average preceding splat at that position has solidified, i.e. generally not less than 10 traverses per second. Otherwise, the resulting structure will be layered with bands of spray cast (molten preceding splat surface) interleaved with bands of spray deposited metal (solidified preceding splat surface), which is undesirable as it leads to heterogeneity. With fast enough scanning, visual obser- GB 2 153 392A 3 monitors and enable the necessary control of the process. Scanning, however, is amenable to an alternative mode of control, v;z. programming to ensure incremental casting at any given point, as already mentioned.
In i nd ustria kscale operation of the process, the deposit is always completely solid (i.e. temperature below the solidus) very soon after leaving the deposition area. This allows the product to be hot rolled "in line" without any danger of "hot tearing" or "hot shortness" as would be caused by plastic deformation if the deposit were above the solidus.
The invention will be described by way of example with reference to the accompanying drawing, which illustrates a slab being spraydeposited, with certain features greatly enlarged for clarity.
A spray head 1 produces a narrow cone of molten metal spray directed towards a cooled substrate 2, on which the resulting coating of metal may be hot-rolled or from which it may be stripped. The spray head 1 is to deposit a thick slab of metal, say 5 cm thick. The spray head moves back and forth parallel to the z- axis. The substrate lies in the x-y plane, and is withdrawn relatively slowly in the x direction.
The spray is directed in the x-y plane, at 45 to the x-direction.
It can be shown that the profile 3 of the edge of the deposited layer should theoreti cally approach as closely as possible the form of a parabola. This would be impossible if the spray were applied in purely the y-direction and therefore, instead, it is applied with a substantial x-component, although, as indicated in the drawing, the actual profile deviates from a parabola.
The parabola shape can be seen to be intuitively reasonable since, at the very leading edge, molten droplets will directly strike the substrate-the coolest surface of all-and will freeze faster than 'incremental solidification' unless a fair thickness is applied quickly, whereas nearer the top of the deposition hill, heat extraction is slower and only a smaller thickness can be applied before exceeding the molten thickness tolerable as 'incremental solidification'.
The deposition zone can be extended for thicker deposits so long as some approximateion to the square root law (i.e. parabola shape) is programmed, but eventually the deposition rate would become unpractically low. However gas convection and radiation heat transfer extends the practical upper limit of thickness of deposit. In the case of lowmelting metals, heat loss by radiation is not important but gas convection becomes domi- nant at greater thicknesses.
In practice, incremental solidification conditions can be maintained through a substantial proportion of the thickness deposited, even though the deposition rate departs signifi- vation or radiation pyrometry will be effective 130 cantly from the ideal, demonstrating that there 4 GB 2 153 392A 4 is a useful tolerance on the flow rate profile and on the thickness of the liquid layer.
Control can be applied by varying the distance between the spray head 1 and the substrate 2. The solid angle of the spray from the spray head 1 could also be varied. The thickness applied in any one pass can also be controlled by the speed of scanning and by the speed of advance of the substrate 1.
Claims (9)
1. A process of producing a metal body, comprising atomising a source of molten metal and directing the atomised molten metal particles, as a spray, onto a cooler substrate, an which the molten metal particles splat and build up to form a deposit, characterised by controlling the spray conditions so that the whole, or most, of the surface of the deposit is molten throughout the process.
2. A process according to Claim 1, wherein the metal body produced is strip sheet.
3. A process according to Claim 1 or 2, wherein deposit is subsequently removed from the substrate.
4. A process according to any preceding claim, wherein the deposit is hot worked.
5. A process according to any preceding claim, wherein the spray conditions are controlled by a programme which scans the directed stream over a desired area of the substrate such that, at every point in that area, the average droplet lands on the preced- ing droplet on the substrate while at least the top surface of that droplet is still molten but the thickness of molten metal does not increase beyond what is restrainable by the surface tension and viscosity of the molten metal.
6. A process according to Claim 5, wherein the programme maintains the deposit at a thickness which at a given point is approximately proportional to the square root of the distance of that point from the leading edge of the deposit.
7. A process according to Claim 5 or 6, wherein the stream of droplets strikes the substrates at an angle measured in a plane which does not include the leading edge of the deposit.
8. A process according to any of Claims 1 to 4, wherein the appearance of the surface of the deposit is monitored, and the spray condi- tions are controlled in response to the monitoring so that the whole, or most, of the surface of the deposit is molten throughout the process.
9. A process according to Claim 8, wherein the directed stream is scanned over a desired area of the substrate such that, at every point in that area, the average droplet lands on the preceding droplet on the substrate while at least the top surface of that droplet is still molten but the thickness of molten metal does not increase beyond what is restrainable by the surface tension and viscosity of the molten metal.
Printed in the United Kingdom for Her Majesty's Stationery Office, Dd 8818935. 1985, 4235 Published at The Patent Office. 25 Southampton Buildings. London. WC2A l AY- from which copies may be obtained.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB848400661A GB8400661D0 (en) | 1984-01-11 | 1984-01-11 | Spray deposition of metal |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8500490D0 GB8500490D0 (en) | 1985-02-13 |
GB2153392A true GB2153392A (en) | 1985-08-21 |
GB2153392B GB2153392B (en) | 1987-06-10 |
Family
ID=10554823
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB848400661A Pending GB8400661D0 (en) | 1984-01-11 | 1984-01-11 | Spray deposition of metal |
GB08500490A Expired GB2153392B (en) | 1984-01-11 | 1985-01-09 | Spray deposition of metal |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB848400661A Pending GB8400661D0 (en) | 1984-01-11 | 1984-01-11 | Spray deposition of metal |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0151511A1 (en) |
JP (1) | JPS60159162A (en) |
GB (2) | GB8400661D0 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2172900A (en) * | 1985-03-25 | 1986-10-01 | Osprey Metals Ltd | Making thixotropic metal by spray casting |
GB2174411A (en) * | 1985-04-19 | 1986-11-05 | Nat Res Dev | Metal forming e.g. casting, process and apparatus |
GB2278615A (en) * | 1993-06-04 | 1994-12-07 | Timothy James Fortune | Metal spraying |
GB2319042A (en) * | 1996-11-08 | 1998-05-13 | Monitor Coatings & Eng | Flame spray coating of continuous casting machine components |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992009715A1 (en) * | 1990-11-21 | 1992-06-11 | Leningradskaya Assotsiatsia 'poliplazma' | Method for plasma jet spraying of biologically active coatings on an implant |
US5240061A (en) * | 1990-12-28 | 1993-08-31 | Osprey Metals Limited | Substrate for spray cast strip |
JPH04259368A (en) * | 1991-02-12 | 1992-09-14 | Mitsubishi Heavy Ind Ltd | Manufacture of intermetallic compound sheet |
CN1045636C (en) * | 1995-07-17 | 1999-10-13 | 中南工业大学 | Equipment and process for injection deposition |
DE69724089T2 (en) * | 1996-12-10 | 2004-06-03 | Howmet Research Corp., Whitehall | Spraying method and installation |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB778785A (en) * | 1954-02-18 | 1957-07-10 | Union Carbide & Carbon Corp | Method of applying hard-facing metals |
GB949646A (en) * | 1961-04-07 | 1964-02-19 | Clevite Corp | Improvements in or relating to semiconductor devices |
GB1014383A (en) * | 1962-10-08 | 1965-12-22 | British Oxygen Co Ltd | Hard metal deposits |
GB1117554A (en) * | 1966-03-15 | 1968-06-19 | Lamben Developments Ltd | Improvements in or relating to the galvanization of iron and steel |
GB1228498A (en) * | 1968-01-02 | 1971-04-15 | ||
GB1235135A (en) * | 1967-10-16 | 1971-06-09 | Ytong Internat Ab | Method of carrying out a surface treatment of building units and product treated according to the method |
GB1460285A (en) * | 1972-11-08 | 1976-12-31 | Sfec | Method of metallizing by spraying a metal coating onto an aluminium or aluminium alloy substrate ampholytic compound |
GB1481678A (en) * | 1975-04-11 | 1977-08-03 | Eutectic Corp | Coating of boiler tubes |
GB2000815A (en) * | 1977-07-05 | 1979-01-17 | Union Carbide Corp | Method for forming hard wear-resistant coatings and the coated article produced thereby |
GB1584371A (en) * | 1976-07-07 | 1981-02-11 | Mtu Muenchen Gmbh | Deposition of protective coatings on workpieces |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1262471A (en) * | 1968-05-14 | 1972-02-02 | Nat Res Dev | Improvements relating to the fabrication of articles |
US3995073A (en) * | 1974-04-08 | 1976-11-30 | Trw Inc. | Method for thermal deposition of metal |
FR2334431A1 (en) * | 1975-12-12 | 1977-07-08 | Gen Electric | THERMAL SPRAYING DEPOSIT PROCESS |
US4224356A (en) * | 1977-05-31 | 1980-09-23 | The Secretary For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Deposition of metals on a base |
GB2115014B (en) * | 1982-02-23 | 1985-11-27 | Nat Res Dev | Method of making a two-phase or multi-phase metallic material |
-
1984
- 1984-01-11 GB GB848400661A patent/GB8400661D0/en active Pending
-
1985
- 1985-01-09 EP EP85300138A patent/EP0151511A1/en not_active Withdrawn
- 1985-01-09 GB GB08500490A patent/GB2153392B/en not_active Expired
- 1985-01-11 JP JP60003907A patent/JPS60159162A/en active Pending
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB778785A (en) * | 1954-02-18 | 1957-07-10 | Union Carbide & Carbon Corp | Method of applying hard-facing metals |
GB949646A (en) * | 1961-04-07 | 1964-02-19 | Clevite Corp | Improvements in or relating to semiconductor devices |
GB1014383A (en) * | 1962-10-08 | 1965-12-22 | British Oxygen Co Ltd | Hard metal deposits |
GB1117554A (en) * | 1966-03-15 | 1968-06-19 | Lamben Developments Ltd | Improvements in or relating to the galvanization of iron and steel |
GB1235135A (en) * | 1967-10-16 | 1971-06-09 | Ytong Internat Ab | Method of carrying out a surface treatment of building units and product treated according to the method |
GB1228498A (en) * | 1968-01-02 | 1971-04-15 | ||
GB1460285A (en) * | 1972-11-08 | 1976-12-31 | Sfec | Method of metallizing by spraying a metal coating onto an aluminium or aluminium alloy substrate ampholytic compound |
GB1481678A (en) * | 1975-04-11 | 1977-08-03 | Eutectic Corp | Coating of boiler tubes |
GB1584371A (en) * | 1976-07-07 | 1981-02-11 | Mtu Muenchen Gmbh | Deposition of protective coatings on workpieces |
GB2000815A (en) * | 1977-07-05 | 1979-01-17 | Union Carbide Corp | Method for forming hard wear-resistant coatings and the coated article produced thereby |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2172900A (en) * | 1985-03-25 | 1986-10-01 | Osprey Metals Ltd | Making thixotropic metal by spray casting |
US4804034A (en) * | 1985-03-25 | 1989-02-14 | Osprey Metals Limited | Method of manufacture of a thixotropic deposit |
GB2174411A (en) * | 1985-04-19 | 1986-11-05 | Nat Res Dev | Metal forming e.g. casting, process and apparatus |
GB2174411B (en) * | 1985-04-19 | 1989-06-28 | Nat Res Dev | Metal casting |
GB2278615A (en) * | 1993-06-04 | 1994-12-07 | Timothy James Fortune | Metal spraying |
GB2319042A (en) * | 1996-11-08 | 1998-05-13 | Monitor Coatings & Eng | Flame spray coating of continuous casting machine components |
GB2319042B (en) * | 1996-11-08 | 1998-11-11 | Monitor Coatings & Eng | Coating of continuous casting machine components |
Also Published As
Publication number | Publication date |
---|---|
GB8500490D0 (en) | 1985-02-13 |
EP0151511A1 (en) | 1985-08-14 |
JPS60159162A (en) | 1985-08-20 |
GB2153392B (en) | 1987-06-10 |
GB8400661D0 (en) | 1984-02-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1102186A (en) | Process of hot-dip galvanizing and alloying | |
US5017250A (en) | Copper alloys having improved softening resistance and a method of manufacture thereof | |
EP0172030B1 (en) | Flow coating of metals | |
CA1124142A (en) | Finishing method and apparatus for conventional hot dip coating of a ferrous base metal strip with a molten coating metal | |
GB2153392A (en) | Spray deposition of metal | |
EP0308435B1 (en) | A method for controlling the thickness of an intermetallic layer on a continuous steel product in a continuous hot-dip galvanizing process | |
Blackford et al. | Spray deposition of an iron aluminide | |
US4971842A (en) | Method for controlling the thickness of an intermetallic layer on a continuous steel product in a continuous hot-dip galvanizing process | |
US4513033A (en) | Differentially coated galvanized steel strip and method and apparatus for producing same | |
WO1980000977A1 (en) | Process of producing one-side alloyed galvanized steel strip | |
CA1303916C (en) | Zn-al hot-dip galvanized steel sheet having improved resistance against secular peeling and method for producing the same | |
US2715252A (en) | Continuous casting apparatus for aluminum onto metallic strip material | |
JP3888784B2 (en) | Edge wrinkle prevention method for hot-dip Zn-based plated steel sheet | |
US5722151A (en) | Process for making semi-finished products | |
US5039478A (en) | Copper alloys having improved softening resistance and a method of manufacture thereof | |
US4528935A (en) | Differentially coated galvanized steel strip and method and apparatus for producing same | |
US6024778A (en) | Production of iron or nickel-based products | |
JP2608502B2 (en) | Manufacturing method of hot-dip aluminized steel sheet with reduced spangle pattern | |
JPH10237613A (en) | Hot-dip zinc-aluminum alloy coated steel sheet excellent in surface smoothness, and its production | |
KR100276323B1 (en) | Prevention of dross adhesion to hot dip galvanized surface | |
US4588658A (en) | Differentially coated galvanized steel strip | |
JPH08144037A (en) | Method and apparatus for producing molten aluminum-zinc alloy plated steel sheet | |
Patil et al. | Minispangling of hot dip galvanized steel | |
JPH07224367A (en) | Production of hot-dip al plated steel sheet having zn-diffused layer | |
JPH11124660A (en) | Hot dip zn-al alloy plated steel sheet excellent in surface smoothness and its production |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |