EP0646658A1 - Galvanizing bath members effectively protected against the deposition of alloy layers, a process for producing said members, and a method of hot-dip galvanizing that uses said members - Google Patents
Galvanizing bath members effectively protected against the deposition of alloy layers, a process for producing said members, and a method of hot-dip galvanizing that uses said members Download PDFInfo
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- EP0646658A1 EP0646658A1 EP94113648A EP94113648A EP0646658A1 EP 0646658 A1 EP0646658 A1 EP 0646658A1 EP 94113648 A EP94113648 A EP 94113648A EP 94113648 A EP94113648 A EP 94113648A EP 0646658 A1 EP0646658 A1 EP 0646658A1
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- alloy layers
- galvanizing bath
- aluminum
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- 229910045601 alloy Inorganic materials 0.000 title claims abstract description 35
- 239000000956 alloy Substances 0.000 title claims abstract description 35
- 238000005246 galvanizing Methods 0.000 title claims abstract description 25
- 230000008021 deposition Effects 0.000 title claims abstract description 23
- 238000000034 method Methods 0.000 title claims abstract description 18
- 230000008569 process Effects 0.000 title claims abstract description 10
- 238000000576 coating method Methods 0.000 claims abstract description 36
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 22
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 22
- 230000003628 erosive effect Effects 0.000 claims abstract description 12
- 239000000919 ceramic Substances 0.000 claims abstract description 11
- 239000000843 powder Substances 0.000 claims abstract description 6
- 239000011248 coating agent Substances 0.000 claims description 23
- 238000007751 thermal spraying Methods 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 14
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 12
- 229910052725 zinc Inorganic materials 0.000 claims description 12
- 239000011701 zinc Substances 0.000 claims description 12
- 239000011159 matrix material Substances 0.000 claims description 11
- 229910000831 Steel Inorganic materials 0.000 claims description 10
- 239000010959 steel Substances 0.000 claims description 10
- 239000011195 cermet Substances 0.000 claims description 9
- 229910052596 spinel Inorganic materials 0.000 claims description 6
- 239000011029 spinel Substances 0.000 claims description 6
- 229910052845 zircon Inorganic materials 0.000 claims description 5
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims description 4
- 238000005507 spraying Methods 0.000 claims 2
- 229910001297 Zn alloy Inorganic materials 0.000 abstract description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 9
- 229910052742 iron Inorganic materials 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 4
- 229910000611 Zinc aluminium Inorganic materials 0.000 abstract description 3
- HXFVOUUOTHJFPX-UHFFFAOYSA-N alumane;zinc Chemical compound [AlH3].[Zn] HXFVOUUOTHJFPX-UHFFFAOYSA-N 0.000 abstract description 3
- 238000004088 simulation Methods 0.000 abstract description 3
- 238000012360 testing method Methods 0.000 abstract description 3
- 239000011253 protective coating Substances 0.000 abstract description 2
- 230000000717 retained effect Effects 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 8
- 229910001335 Galvanized steel Inorganic materials 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000008397 galvanized steel Substances 0.000 description 5
- 229910052574 oxide ceramic Inorganic materials 0.000 description 5
- 239000011224 oxide ceramic Substances 0.000 description 5
- 229910052804 chromium Inorganic materials 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910000765 intermetallic Inorganic materials 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 229910052575 non-oxide ceramic Inorganic materials 0.000 description 3
- 239000011225 non-oxide ceramic Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 229910000640 Fe alloy Inorganic materials 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910009043 WC-Co Inorganic materials 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 230000006911 nucleation Effects 0.000 description 2
- 238000010899 nucleation Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- QYEXBYZXHDUPRC-UHFFFAOYSA-N B#[Ti]#B Chemical compound B#[Ti]#B QYEXBYZXHDUPRC-UHFFFAOYSA-N 0.000 description 1
- 229910019918 CrB2 Inorganic materials 0.000 description 1
- 229910033181 TiB2 Inorganic materials 0.000 description 1
- 229910007570 Zn-Al Inorganic materials 0.000 description 1
- 229910007948 ZrB2 Inorganic materials 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- VWZIXVXBCBBRGP-UHFFFAOYSA-N boron;zirconium Chemical compound B#[Zr]#B VWZIXVXBCBBRGP-UHFFFAOYSA-N 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052909 inorganic silicate Inorganic materials 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229910003470 tongbaite Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
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- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Images
Classifications
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- 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
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/10—Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
-
- 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/003—Apparatus
- C23C2/0034—Details related to elements immersed in bath
- C23C2/00342—Moving elements, e.g. pumps or mixers
- C23C2/00344—Means for moving substrates, e.g. immersed rollers or immersed bearings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D17/00—Constructional parts, or assemblies thereof, of cells for electrolytic coating
- C25D17/02—Tanks; Installations therefor
- C25D17/04—External supporting frames or structures
Definitions
- This invention relates to the development of a means that is effective in preventing the deposition of alloy layers on the surfaces of members, such as sunk rolls and Support rolls, that are used as submerged in zinc baths or zinc-aluminum alloy baths in facilities for the production of galvanized steel plates and sheets. More specifically, the invention relates to galvanizing bath members such as those to be submerged in galvanizing baths that have many chances to contact the molten zinc and which have coatings deposited on their surfaces by thermal spraying in order to impart not only high resistance to the erosive action of the molten zinc but also effective protection against the deposition of alloy layers. The invention also relates to a process for producing said galvanizing bath members, as well as a method of hot-dip galvanizing that uses said bath members.
- Galvanized steel plates and sheets have primarily been produced by continuous hot-dip galvanizing, in which a steel strip with cleaned surfaces is passed through a molten zinc alloy bath usually containing 0.1 - 0.2% aluminum, has the direction of its travel changed by a sunk (submerged) roll and passes by support rolls, wiping nozzles, etc. to be sent to a heating furnace, where alloying is effected and furnace-cooled to room temperature.
- the iron will dissolve out of the steel strip to be transferred into the molten zinc alloy, forming an Fe- and Al- supersaturated region in the liquid phase between the surfaces of the steel strip and the sunk roll.
- the coatings formed by thermal spraying the Conventional oxide ceramics have high resistance not only to the erosive action of molten zinc but also against the deposition of unwanted alloy layers.
- the thermal expansion coefficient and mechanical strength of the coatings are so small that if they are actually applied to the surfaces of sunk rolls and other steel rolls, cracks will often develop, making them unsuitable as protective coatings.
- the coatings formed by thermal spraying non-oxide ceramics are as poor in adhesion and mechanical strength as those formed by thermal spraying the oxide ceramics.
- the addition of metallic components is essential.
- the coatings formed by thermal spraying the mixtures with Co, Ni or Cr were eroded by either alloying with the galvanizing metal or reacting with diffusing added elements; alternatively, the addition of Co, Ni or Cr promoted the formation of alloy layers deposits on the surface of the coatings.
- the coating formed by spray fusing the 22% AI-containing iron alloy taught in Unexamined Published Japanese Patent Application (kokai) Hei 5-78801 is an intermetallic compound of the same kind as the alloy layers to be deposited on the roll surface and, hence, the use of this alloy often induced the deposition of unwanted alloy layers.
- the present invention has been accomplished under these circumstances and has as an object providing such an article for use either submerged in molten zinc baths or in contact with the molten zinc during continuous hot-dip galvanizing that it has a thermal sprayed coating that not only has high resistance to the molten zinc alloy but is also protected effectively against the deposition of unwanted alloy layers.
- Another object of the invention is to provide a process for producing said article.
- Still another object of the invention is to provide a method of hot-dip galvanizing that employs said article as a sunk roll or support rolls in the production of galvanized steel plates or sheets and thereby assures maximum protection against the deposition of unwanted alloy layers on the surfaces of those rolls.
- the present inventors made studies to attain these objects of the invention and formed coatings using various thermal spraying materials. And in order to investigate the deposition profile of unwanted alloy layers formed on the surfaces of the coatings during hot-dip galvanizing, the inventors conducted a simulation with an experimental setup of the type shown in Fig. 1 and to be described below in details in Example 1. Based on the results of the simulation, the inventors analyzed and evaluated the alloy layers that deposited on the surfaces of test samples.
- Fig. 1 is a schematic section of the experimental setup which was used not only in Examples 1 and 2 but also in Comparative Examples 1 - 4 to simulate the process of the formation of alloy layers on test samples.
- the alloy layers deposited on the surfaces of sunk rolls and support rolls are mostly made of an intermetallic Zn-Fe-AI compound.
- the deposition of the Zn-Fe-AI alloy layer starts with the dissolution of iron from the steel strip into the molten zinc alloy, goes through the formation of an Fe- and Al- supersaturated region in the liquid phase between the surfaces of the steel strip and the sunk roll, and ends with the nucleation of the supersaturated metallic components on the roll surface.
- Papers on nucleation have pointed out that its frequency is generally determined by the matching in Crystalline structure on the surface of the material in which nuclei are to be formed, namely, the crystal matching between the surface of hot material and the precipitate, and by the surface tension of the material.
- the coating formed by thermal spraying an oxide Ceramic or Mo-base cermet matrix that already has high resistance to the erosive action of molten zinc alloys and to which aluminum has been added in such an amount as to give 0.5 - 10 wt% AI in the as-sprayed state has not only outstanding resistance to molten zinc alloys but it also is protected effectively against the deposition of unwanted alloy layers. If the addition of aluminum is less than 0.5 wt%, the proportion of AI that occupies the coating's surface is too small to assure satisfactory protection against the deposition of unwanted alloy layers; if the addition of aluminum exceeds 10 wt%, aluminum will dissolve out of steel plates or sheets in an excessive amount to potentially cause adverse effects on their quality.
- the coating formed by thermal spraying it in the presence of the specified amount of AI is not only protected effectively against the deposition of intermetallic compounds but also improved in adherence and mechanical strength.
- Aluminum has a much lower melting point than ceramics and cermets and if a given amount of aluminum as mixed with a ceramic or cermet powder is thermally sprayed, a significant portion of the sprayed aluminum will be evaporated or lost upon impinging on the substrate surface.
- the amount of aluminum that remains in the thermal sprayed coating varies with the type of the spray method used and it is necessary to control the feed's formulation in such a way that the amount of residual aluminum will be at a preset level. This is why the range of aluminum addition to ceramics or cermets is specified by "weight percent in the as-sprayed state".
- Fig. 1 is a schematic presentation of the experimental setup which was used not only in Examples 1 and 2 but also in Comparative Examples 1 - 4. The following description should be read with reference to Fig. 1.
- a heater 1 holds the interior of a furnace 8 at a predetermined temperature.
- a crucible 4 placed on a table 6 in the bottom of the furnace 8 contains a molten zinc-aluminum alloy 5.
- a SUS rod (20 mm ⁇ x 120 mm L ) coupled and retained by a rotating shaft 9 is thermally sprayed with Mo-MoB + AI to prepare a thermal sprayed sample 2, which is mounted rotatably in a soft iron cylinder 3 having a window 7.
- the thermal sprayed sample was rotated for 6 hours and its surface was examined under a microscope (X 30) and the severity of the deposition of alloyed layers was evaluated by counting the number of Zn-Fe-AI base precipitates (number of dross deposits) as identified within the visual field, as well as measuring their size ( size of dross deposits).
- Example 1 The procedure of Example 1 was repeated except that spinel + AI was substituted as a thermal spraying material.
- the thermal sprayed sample 2 thus prepared was immersed in the molten Zn-Al bath 5 and the severity of the deposition of alloyed layers was evaluated as in Example 1.
- Example 1 Using the same experimental Setup as in Example 1, the procedure of Example 1 was repeated except that the thermal spraying material was Mo-MoB (Comparative Example 1), Fe-Al (Comparative Example 2), A1 2 0 3 + Ti0 2 (Comparative Example 3)and WC-Co(Comparative Example 4). After 6 hours of the experiment, the number of dross deposits was counted and their size was measured.
- the thermal sprayed coating of the present invention comprises a ceramic or cermet matrix having high resistance to the erosive action of molten zinc alloys and which has aluminum added thereto in an amount of 0.5 - 10 wt% in the as-sprayed composition.
- the coating offers the advantage that if it is applied to a sunk roll and other bath members that are to be used submerged in the molten zinc bath during Continuous hot-dip galvanizing, those members are not only provided with high resistance to the erosive action of molten zinc alloys but also protected very effectively against the deposition of unwanted alloy layers which would otherwise form on the bath members during galvanizing by the prior art.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Electrochemistry (AREA)
- Coating By Spraying Or Casting (AREA)
- Coating With Molten Metal (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Abstract
Description
- This invention relates to the development of a means that is effective in preventing the deposition of alloy layers on the surfaces of members, such as sunk rolls and Support rolls, that are used as submerged in zinc baths or zinc-aluminum alloy baths in facilities for the production of galvanized steel plates and sheets. More specifically, the invention relates to galvanizing bath members such as those to be submerged in galvanizing baths that have many chances to contact the molten zinc and which have coatings deposited on their surfaces by thermal spraying in order to impart not only high resistance to the erosive action of the molten zinc but also effective protection against the deposition of alloy layers. The invention also relates to a process for producing said galvanizing bath members, as well as a method of hot-dip galvanizing that uses said bath members.
- Galvanized steel plates and sheets have primarily been produced by continuous hot-dip galvanizing, in which a steel strip with cleaned surfaces is passed through a molten zinc alloy bath usually containing 0.1 - 0.2% aluminum, has the direction of its travel changed by a sunk (submerged) roll and passes by support rolls, wiping nozzles, etc. to be sent to a heating furnace, where alloying is effected and furnace-cooled to room temperature.
- During the passage of the steel strip through the aluminum-containing molten zinc alloy bath, the iron will dissolve out of the steel strip to be transferred into the molten zinc alloy, forming an Fe- and Al- supersaturated region in the liquid phase between the surfaces of the steel strip and the sunk roll. The metallic components precipitated out of this liquid phase supersaturated with Fe and AI nucleate on the surface of the sunk roll to have alloy layers deposited in solid phase, which is a phenomenon generally referred to as "dross formation".
- The solid-phase deposits of such alloy layers are hard and adhere to the sunk roll so tenaceously that they are deleterious to the surface quality of high-grade galvanized steel sheets such as those for use in automotive body parts. Therefore, preventing the alloy layers from being deposited on the surfaces of sunk rolls and support rolls is extremely important in the effort to improve the quality of galvanized steel plates or sheets.
- With a view to preventing the deposition of unwanted alloy layers, it has been proposed that specified materials be thermal sprayed onto the surfaces of sunk rolls or support rolls. The thermal spraying has two functions, one is to prevent the erosion of the surfaces of steel rolls by the molten zinc alloy and the other is to prevent the formation of unwanted alloy layers that are deposited on roll surfaces. Many proposals on the first approach have already been made, as exemplified by the use of non-oxide ceramics (e.g. Cr3C2, WC and TiC) or cermets (e.g. TiB2, CrB2, ZrB2) in Unexamined Published Japanese Patent Application (kokai) Hei 4-116147. As for the second approach, the use of a 22% AI-containing iron alloy layer on the surface of a roll has been proposed in Unexamined Published Japanese Patent Application (kokai) Hei 5-78801 whereas the use of an A1203-TiO2 pseudo-binary metal oxide System as a thermal spraying material has been proposed in Unexamined Published Japanese Patent Application (kokai) Hei 5-106011.
- The coatings formed by thermal spraying the Conventional oxide ceramics have high resistance not only to the erosive action of molten zinc but also against the deposition of unwanted alloy layers. However, the thermal expansion coefficient and mechanical strength of the coatings are so small that if they are actually applied to the surfaces of sunk rolls and other steel rolls, cracks will often develop, making them unsuitable as protective coatings.
- The coatings formed by thermal spraying non-oxide ceramics are as poor in adhesion and mechanical strength as those formed by thermal spraying the oxide ceramics. To solve this problem, the addition of metallic components is essential. For example, it has been proposed in Unexamined Published Japanese Patent Application (kokai) Hei 4-358055 that at least one element selected from among Co, Ni and Cr be added to non-oxide ceramics or carbides. As it turned out, however, the coatings formed by thermal spraying the mixtures with Co, Ni or Cr were eroded by either alloying with the galvanizing metal or reacting with diffusing added elements; alternatively, the addition of Co, Ni or Cr promoted the formation of alloy layers deposits on the surface of the coatings.
- The coating formed by spray fusing the 22% AI-containing iron alloy taught in Unexamined Published Japanese Patent Application (kokai) Hei 5-78801 is an intermetallic compound of the same kind as the alloy layers to be deposited on the roll surface and, hence, the use of this alloy often induced the deposition of unwanted alloy layers.
- Thus, all of the conventional thermal sprayed or spray fused coatings have been unsatisfactory in terms of resistance to the deposition of unwanted alloy layers.
- The present invention has been accomplished under these circumstances and has as an object providing such an article for use either submerged in molten zinc baths or in contact with the molten zinc during continuous hot-dip galvanizing that it has a thermal sprayed coating that not only has high resistance to the molten zinc alloy but is also protected effectively against the deposition of unwanted alloy layers.
- Another object of the invention is to provide a process for producing said article.
- Still another object of the invention is to provide a method of hot-dip galvanizing that employs said article as a sunk roll or support rolls in the production of galvanized steel plates or sheets and thereby assures maximum protection against the deposition of unwanted alloy layers on the surfaces of those rolls.
- The present inventors made studies to attain these objects of the invention and formed coatings using various thermal spraying materials. And in order to investigate the deposition profile of unwanted alloy layers formed on the surfaces of the coatings during hot-dip galvanizing, the inventors conducted a simulation with an experimental setup of the type shown in Fig. 1 and to be described below in details in Example 1. Based on the results of the simulation, the inventors analyzed and evaluated the alloy layers that deposited on the surfaces of test samples. They continued their studies intensively such as by analyzing the mechanism behind the formation of the deposited alloy layers and found that the coatings formed by thermal spraying oxide ceramic or Mo-base cermet matrix that already had high resistance to the erosive action of molten zinc alloy and to which aluminum was added in such an amount as to give 0.5 - 10 wt% AI in the as-sprayed compositon could be protected very effectively against the deposition of alloy layers such as an intermetallic Zn-Fe-AI compound.
- Fig. 1 is a schematic section of the experimental setup which was used not only in Examples 1 and 2 but also in Comparative Examples 1 - 4 to simulate the process of the formation of alloy layers on test samples.
- The alloy layers deposited on the surfaces of sunk rolls and support rolls are mostly made of an intermetallic Zn-Fe-AI compound. As already mentioned, the deposition of the Zn-Fe-AI alloy layer starts with the dissolution of iron from the steel strip into the molten zinc alloy, goes through the formation of an Fe- and Al- supersaturated region in the liquid phase between the surfaces of the steel strip and the sunk roll, and ends with the nucleation of the supersaturated metallic components on the roll surface. Papers on nucleation have pointed out that its frequency is generally determined by the matching in Crystalline structure on the surface of the material in which nuclei are to be formed, namely, the crystal matching between the surface of hot material and the precipitate, and by the surface tension of the material.
- Details of the mechanism behind the effectiveness of AI addition are not completely clear but it may well be assumed that the added aluminum affects the crystal matching at the surface of the material or its surface tension and, thereby, lowers the frequency of the formation of nuclei of the alloy which would otherwise occur and that, as a result, the chance of dross formation on the roll surfaces having the thermal sprayed coating is reduced.
- The coating formed by thermal spraying an oxide Ceramic or Mo-base cermet matrix that already has high resistance to the erosive action of molten zinc alloys and to which aluminum has been added in such an amount as to give 0.5 - 10 wt% AI in the as-sprayed state has not only outstanding resistance to molten zinc alloys but it also is protected effectively against the deposition of unwanted alloy layers. If the addition of aluminum is less than 0.5 wt%, the proportion of AI that occupies the coating's surface is too small to assure satisfactory protection against the deposition of unwanted alloy layers; if the addition of aluminum exceeds 10 wt%, aluminum will dissolve out of steel plates or sheets in an excessive amount to potentially cause adverse effects on their quality.
- If the oxide ceramic matrix is spinel (MgA1204) or zircon (ZrSi04), the coating formed by thermal spraying it in the presence of the specified amount of AI is not only protected effectively against the deposition of intermetallic compounds but also improved in adherence and mechanical strength.
- Sunk rolls on the surface of which a coating has been formed by thermal spraying Mo-base cermets containing MoB, Mo2 B or Mo2Bs have high resistance to molten zinc but, in actual use, the intermetallic Zn-Fe-Al compound will deposit and can be a serious potential trouble. Hence, after their development as thermal spraying materials having extremely high resistance to molten zinc alloys, the Mo-base cermets containing MoB, Mo2B or Mo2 B5 have been limited in actual use. However, this problem is completely solved by the present invention and it has been found that the deposition of the intermetallic compound can be prevented very effectively by forming a thermal sprayed coating that has AI added to said Mo-base cermets in such an amount that 0.5 - 10 wt%, say, 2 wt% AI will eventually be incorporated in the coating.
- Aluminum has a much lower melting point than ceramics and cermets and if a given amount of aluminum as mixed with a ceramic or cermet powder is thermally sprayed, a significant portion of the sprayed aluminum will be evaporated or lost upon impinging on the substrate surface. In other words, the amount of aluminum that remains in the thermal sprayed coating varies with the type of the spray method used and it is necessary to control the feed's formulation in such a way that the amount of residual aluminum will be at a preset level. This is why the range of aluminum addition to ceramics or cermets is specified by "weight percent in the as-sprayed state".
- The following examples are provided for the purpose of further illustrating the present invention but are in no way to be taken as limiting.
- Fig. 1 is a schematic presentation of the experimental setup which was used not only in Examples 1 and 2 but also in Comparative Examples 1 - 4. The following description should be read with reference to Fig. 1.
- A heater 1 holds the interior of a
furnace 8 at a predetermined temperature. Acrucible 4 placed on a table 6 in the bottom of thefurnace 8 contains a molten zinc-aluminum alloy 5. A SUS rod (20 mmφ x 120 mmL) coupled and retained by a rotatingshaft 9 is thermally sprayed with Mo-MoB + AI to prepare a thermal sprayedsample 2, which is mounted rotatably in asoft iron cylinder 3 having awindow 7. - With a hydrogen-nitrogen atmosphere introduced into the furnace and held at 460 - 550 ° C, the thermal sprayed sample was rotated for 6 hours and its surface was examined under a microscope (X 30) and the severity of the deposition of alloyed layers was evaluated by counting the number of Zn-Fe-AI base precipitates (number of dross deposits) as identified within the visual field, as well as measuring their size ( size of dross deposits).
- The results of the experiment are shown in Table 1.
- The procedure of Example 1 was repeated except that spinel + AI was substituted as a thermal spraying material. The thermal sprayed
sample 2 thus prepared was immersed in the molten Zn-Al bath 5 and the severity of the deposition of alloyed layers was evaluated as in Example 1. - The results of the experiment are also shown in Table 1.
- Using the same experimental Setup as in Example 1, the procedure of Example 1 was repeated except that the thermal spraying material was Mo-MoB (Comparative Example 1), Fe-Al (Comparative Example 2), A1203 + Ti02 (Comparative Example 3)and WC-Co(Comparative Example 4). After 6 hours of the experiment, the number of dross deposits was counted and their size was measured.
-
- As one can see from Table 1, the comparative samples with the coatings formed by thermal spraying of Mo-MoB and Fe-Al, respectively, had Fe-Al dross deposited in fairly large quantities on their surface. The comparative sample with the coating formed by thermal spraying of WC-Co had dross deposited over the entire surface.
- In contrast, the sample with the coating formed by thermal spraying of Mo-MoB plus 2 wt% AI (in the as-sprayed coating), as well as the sample with the coating formed by thermal spraying of spinel plus 2 wt% AI had much fewer dross deposits of smaller size than the comparative sample with the coating formed by thermal spraying of Al2O3 +Ti02 ceramics.
- Additional experiments were conducted by replacing spinel with zircon (ZrO2·SiO2 or Zr. Si04) and the results were essentially the same.
- As described on the foregoing pages, the thermal sprayed coating of the present invention comprises a ceramic or cermet matrix having high resistance to the erosive action of molten zinc alloys and which has aluminum added thereto in an amount of 0.5 - 10 wt% in the as-sprayed composition. The coating offers the advantage that if it is applied to a sunk roll and other bath members that are to be used submerged in the molten zinc bath during Continuous hot-dip galvanizing, those members are not only provided with high resistance to the erosive action of molten zinc alloys but also protected very effectively against the deposition of unwanted alloy layers which would otherwise form on the bath members during galvanizing by the prior art.
Claims (9)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5240392A JPH0776763A (en) | 1993-09-01 | 1993-09-01 | Member for galvanization bath excellent in resistance to blocking to alloy layer, its preparation and hot dip galvanization therewith |
JP240392/93 | 1993-09-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0646658A1 true EP0646658A1 (en) | 1995-04-05 |
EP0646658B1 EP0646658B1 (en) | 1996-11-06 |
Family
ID=17058803
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP94113648A Expired - Lifetime EP0646658B1 (en) | 1993-09-01 | 1994-08-31 | Galvanizing bath members effectively protected against the deposition of alloy layers, a process for producing said members, and a method of hot-dip galvanizing that uses said members |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0646658B1 (en) |
JP (1) | JPH0776763A (en) |
KR (1) | KR950008724A (en) |
CN (1) | CN1055509C (en) |
DE (1) | DE69400856T2 (en) |
TW (1) | TW287207B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114686796A (en) * | 2020-12-31 | 2022-07-01 | 安泰天龙钨钼科技有限公司 | Wear-resistant corrosion-resistant coating material, coating and preparation method thereof |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10147897C1 (en) * | 2001-09-28 | 2003-01-23 | Epcos Ag | Process for directly galvanizing contact layers onto ceramic components comprises activating the regions to be galvanized using an aqueous solution containing phosphoric acid, and applying the contact layers on the treated components |
JP4408649B2 (en) * | 2003-04-30 | 2010-02-03 | Jfeスチール株式会社 | Dipping member for hot metal plating baths with excellent dross resistance |
CN101734222B (en) * | 2008-11-12 | 2012-11-07 | 晨星软件研发(深圳)有限公司 | Monitoring device and operation method thereof |
GB2484302A (en) * | 2010-10-05 | 2012-04-11 | Rotalok Security Ltd | Seal comprising RFID tag and RFID reader with random number generator |
CN117564387B (en) * | 2024-01-15 | 2024-03-15 | 烟台大学 | Method for preparing dissimilar metal composite structure by rotary hot dip connection and additive |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DZ1422A1 (en) * | 1989-06-09 | 2004-09-13 | Galva Lorraine | Method, procedure and installation for the continuous / intermittent coating of objects by passing said objects through a liquid mass of a coating product. |
CN1071709A (en) * | 1991-10-18 | 1993-05-05 | 中国人民解放军兰州军区空军后勤部科技开发中心 | Compound material thermal galvanization bath |
-
1993
- 1993-09-01 JP JP5240392A patent/JPH0776763A/en active Pending
-
1994
- 1994-08-31 KR KR1019940021802A patent/KR950008724A/en not_active Application Discontinuation
- 1994-08-31 DE DE69400856T patent/DE69400856T2/en not_active Expired - Fee Related
- 1994-08-31 EP EP94113648A patent/EP0646658B1/en not_active Expired - Lifetime
- 1994-08-31 CN CN94117340A patent/CN1055509C/en not_active Expired - Fee Related
- 1994-09-30 TW TW083109038A patent/TW287207B/zh active
Non-Patent Citations (1)
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PATENT ABSTRACTS OF JAPAN * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114686796A (en) * | 2020-12-31 | 2022-07-01 | 安泰天龙钨钼科技有限公司 | Wear-resistant corrosion-resistant coating material, coating and preparation method thereof |
CN114686796B (en) * | 2020-12-31 | 2024-02-13 | 安泰天龙钨钼科技有限公司 | Wear-resistant corrosion-resistant coating material, coating and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0776763A (en) | 1995-03-20 |
DE69400856D1 (en) | 1996-12-12 |
TW287207B (en) | 1996-10-01 |
CN1055509C (en) | 2000-08-16 |
CN1107522A (en) | 1995-08-30 |
KR950008724A (en) | 1995-04-19 |
DE69400856T2 (en) | 1997-05-22 |
EP0646658B1 (en) | 1996-11-06 |
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