WO2010113828A1 - 天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼 - Google Patents
天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼 Download PDFInfo
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- WO2010113828A1 WO2010113828A1 PCT/JP2010/055482 JP2010055482W WO2010113828A1 WO 2010113828 A1 WO2010113828 A1 WO 2010113828A1 JP 2010055482 W JP2010055482 W JP 2010055482W WO 2010113828 A1 WO2010113828 A1 WO 2010113828A1
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/38—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
- C09D5/10—Anti-corrosive paints containing metal dust
- C09D5/106—Anti-corrosive paints containing metal dust containing Zn
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/18—Fireproof paints including high temperature resistant paints
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/58—Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
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- 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
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12535—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.] with additional, spatially distinct nonmetal component
- Y10T428/12556—Organic component
- Y10T428/12569—Synthetic resin
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- 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
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12951—Fe-base component
- Y10T428/12972—Containing 0.01-1.7% carbon [i.e., steel]
Definitions
- the present invention relates to a corrosion resistant steel for chimneys and flues, which is required to have corrosion resistance, in particular, rust resistance, rust adhesion, and local corrosion resistance in a natural gas-fired or liquefied petroleum gas-fired plant.
- Patent Document 1 the component composition of the steel material is C: 0.045% or less, Si: 0.01 to 0.5%, Mn: 0.5 to 2.0%, P: 0.03% or less, S : For cleaning structures containing 0.003% or less, N: 0.020% or less, Cr: 11 to 12.5%, Ni: 0.01 to 2.0% and Cu: 0.05 to 2.0% Stainless steel that exhibits excellent corrosion resistance in a corrosive environment such as SOx and NOx produced in a chimney is disclosed.
- Patent Document 2 discloses an austenitic stainless steel having corrosion resistance 10 times or more that of SS400 steel, almost no rust formation, and good weldability.
- the component composition of steel materials is as follows: C: 0.04 to 0.15%, Si: 0.05 to 1.0%, Mn: 0.2 to 1.7%, Cr: more than 6% 11 Chimney / flue steel containing less than 10% and Al: 0.07% or less is disclosed.
- 5% Cr steel is used as a base, impurity S is reduced to 0.010% or less, Ti is added in the range of 0.005 to 0.05%, and Ni is further added to 1.0%.
- Patent Document 5 the chemical component is excellent in corrosion resistance in a carbon dioxide-containing condensate environment in which Cr: 0.4 to 6%, Cu: 0.1 to 1%, and Al: 0.005 to 0.1% are controlled.
- Steel materials are disclosed.
- the rust layer generated on the steel material is easily peeled off. Therefore, in this document, not only the rust prevention effect is low, but also the problem that the peeled off powdery or thin-skinned iron hydroxide scatters from the chimney to the outside and harms the environment is an issue to be solved. Has arrived.
- the component composition of a steel material is Si: 0.01% or less and less than 1.2%, Mn: 0.02 to 2.0%, Cr: 5.5 to 9.9%, Al: 0.00. Containing 3 to 3.0%, C: 0.02 or less, P: 0.03% or less, S: 0.01% or less, N: 0.02% Further, there is disclosed a corrosion-resistant steel for exhaust systems of internal combustion engines such as automobiles and ships, in which a metal having a low potential is coated to a thickness of 0.5 to 50 ⁇ m.
- Patent Documents 7 to 9 describe steel having excellent corrosion resistance in a corrosive environment such as a condensation corrosion environment, an atmospheric corrosion environment, a tap water corrosion environment, a concrete corrosion environment, and a seawater corrosion environment as well as excellent weld toughness. Steel containing 4 to 9%, 2 to 7% and 3 to 11% of Cr, and 0.1 to 5%, 0.1 to 2% and 0.1 to 2% of Al, respectively. The invention is disclosed. In addition, as shown in Patent Document 10, an attempt from a low alloy steel as a sulfuric acid dew point corrosion resistant steel has also been proposed.
- JP 2002-285296 A JP-A-8-311621 Japanese Patent Laid-Open No. 10-60600 JP-A-9-59749 JP-A-8-291365 JP-A-6-280048 JP 2004-162119 A JP 2004-162121 A International Publication WO2005 / 087964A1 JP 2001-164335 A
- Patent Document 1 and Patent Document 2 are excellent in corrosion resistance and rust resistance, there is a problem of selective local corrosion of the weld heat affected zone, and it is not economical and cost reduction is desired. It was.
- the steel material of Patent Document 3 is low in cost and excellent in corrosion resistance, rust scattering to the surrounding environment once the problem of environmental pollution due to on-site painting, or once coating deterioration or corrosion thinning occurs. There is a problem that cannot be suppressed, and further improvement has been demanded.
- the steel material of Patent Document 4 has excellent rust peel resistance and shows good results in rust scattering and corrosion thinning due to the effects of dew condensation associated with chimney operation.
- the adhesion of rust declined, and it was necessary to periodically remove and remove the rust generated on the inner surface of the chimney and flue, and further improvements were required.
- rainwater enters the chimney during non-operation it becomes a problem to promote the generation of rust in the chimney and flue, and further improvement has been demanded.
- the steel material of Patent Document 5 the rust layer generated on the steel material is peeled off, and powdered or thin-skinned iron hydroxide is scattered from the chimney to the outside, and the environment can be suppressed to some extent. Was not enough, and further improvements were sought by the industry.
- Natural gas or liquefied petroleum gas-fired plant chimneys and flues are exposed to a specific corrosive gas environment with a high concentration of carbon dioxide in the exhaust gas. Wet and dry are repeated in the flue. Furthermore, since the exhaust gas has a large wind pressure, the rust is peeled off, dropped off, and released from the chimney together with the combustion exhaust gas. Therefore, it is necessary to take measures for preventing environmental pollution such as providing a filter and a dust collecting device in the chimney, resulting in an extra cost. Accordingly, in such a chimney / flue of such a plant, measures for preventing local corrosion and rust scattering of the material under the specific corrosion / use environment have been demanded. In addition, as corrosion-resistant steel for chimneys and flues, it is required to ensure the cold workability necessary for processing into chimneys and flues.
- the gist of the present invention aimed at solving the above problems is as follows. (1) In mass%, C: 0.005% or more and 0.030% or less, Si: 0.18% or more and 0.50% or less, Mn: 1.50% or more and less than 3.00, P: 0.030% or less, S: 0.0050% or less, Cr: 4.0% or more and 9.0% or less, Al: 0.20% or more and 1.50% or less, N: 0.020% or less, A natural gas-fired or liquefied petroleum gas-fired plant chimney / flue corrosion resistant steel with excellent rust resistance, rust adhesion, and local corrosion resistance, the balance being Fe and inevitable impurities.
- the present invention applies an inorganic zinc rich primer, so that it has a low alloy composition compared to commercially available stainless steel, but is economical and rust-resistant / rusty. It is a corrosion-resistant steel for chimneys and flues that achieves both high adhesion and local corrosion resistance.
- the chimney / flue steel of the natural gas-fired or liquefied petroleum gas-fired plant of the present invention is, by mass, C: 0.005-0.030%, Si: 0.18-0.50%.
- Mn 1.50 to less than 3.00
- P 0.030% or less
- S 0.0050% or less
- Cr 4.0 to 9.0%
- Al 0.20 to 1.50%
- N 0.020% or less
- the balance being composed of Fe and unavoidable impurities as a basis, and further selectively containing elements that improve properties.
- C 0.005% to 0.030%
- C is an element that improves the strength, and is required to be 0.005% or more.
- the corrosion resistance is deteriorated due to the formation of Cr-based carbides, so the upper limit of the amount added is 0.00. 030%.
- 0.005% or more and 0.020% or less are preferable.
- 0.010% to 0.020% is preferable.
- Si 0.18% to 0.50%
- the content exceeds 0.50%, the effect is saturated and the toughness can be lowered. Therefore, the content range is limited to 0.18% or more and 0.50% or less.
- 0.20% or more and 0.30% or less are preferable.
- [Cr: 4.0% to 9.0%] Cr together with Al described later, needs to contain 4.0% or more in order to ensure corrosion resistance by improving the stability of the passive film, but it is contained in excess of 9.0%.
- the upper limit content is set to 9.0%.
- 5.5% to 7.5% is preferable.
- it is preferably 5.8% or more and 6.3% or less.
- Al is an important element along with Cr in order to ensure corrosion resistance by improving the stability of the passive film.
- the Al content is required to be 0.20% or more from the viewpoint of securing a solid solution Al amount that improves the stability of the passive film.
- the Al content exceeds 1.50%, ferrite phase transformation occurs. Since the temperature range becomes extremely wide and causes slab cracking in the manufacturing process, the content is limited to 0.20% or more and 1.50% or less.
- workability 0.50% or more and 1.30% or less are preferable.
- 0.85% or more and 1.20% or less are preferable.
- Mn mainly serves to ensure strength and to act as an austenite forming element to suppress the formation of coarse ferrite promoted by Cr and Al added from the viewpoint of corrosion resistance.
- Cr and Al are ferrite forming elements, and when they are added in large amounts, they undergo a transformation from solidification to room temperature and become a ferrite single phase structure, resulting in cracks in the slab, Manufacturability is reduced. Therefore, in order to obtain such an effect, it is necessary to add Mn in an amount of 1.50% or more. However, if it is added in an amount of 3.00% or more, the ductility of the base material is remarkably lowered. Addition. In consideration of the strength, manufacturability, weldability, and workability of the steel material, it is preferably 2.00% or more and less than 3.00%.
- N 0.020% or less
- the upper limit is made 0.020% in order to inhibit the ductility and corrosion resistance of the base material due to the formation of nitrides and the like.
- P 0.030% or less
- P is present as an impurity in the steel, but it is desirable that the ductility is lowered and the productivity is not lowered.
- the upper limit content is 0.030%. Furthermore, from the viewpoint of manufacturability and cost, it is preferably 0.020% or less.
- S 0.0050% or less
- S is added in a large amount, the pitting corrosion resistance and local corrosion resistance are lowered, so the smaller one is desirable, and the upper limit content is 0.0050%. Note that S and P are inevitable impurities, and should be reduced as much as possible.
- Cu 0.05% or more and 0.50% or less and Ni: 0.05% or more and 0.50% or less are further added, so that rust resistance / Pitting corrosion resistance and local corrosion resistance can be further improved.
- Mo 0.01% to 0.20%, V: 0.005% to 0.050%, Nb: 0.005% to 0.050%, Ti: 0.005% to 0
- containing any one or more of less than 0.030% further improve rust resistance, pitting corrosion resistance and local corrosion resistance, or improve strength and toughness without affecting corrosion resistance It is possible to make it.
- Cu 0.05% to 0.50%
- Ni 0.05% to 0.50%
- Both Cu and Ni are elements that improve rust resistance, pitting corrosion resistance and local corrosion resistance in the exhaust gas environment of the gas-fired plant, and are added together when added.
- Cu has a greater effect of suppressing rusting and local corrosion than Ni.
- Cu has a surface that is easily segregated. In particular, local Cu segregation parts derived from solidification segregation between dendrites of the cast structure may remain on the product surface.
- both Cu and Ni are added without adding Cu, the increase in the effect of suppressing rusting and local corrosion is small for an increase in cost, but adding both Cu and Ni causes rusting and local corrosion. The effect of suppressing appears remarkably.
- both Cu and Ni are added, the strength is further improved and the effect of suppressing the formation of ferrite is obtained.
- Ni has an effect of preventing ductility and toughness of the base material by preventing slab cracking due to addition of Cu and adding together with Cu.
- Cu and Ni both require addition of 0.05% or more for the manifestation of these effects, but since both add more than 0.50%, embrittlement occurs. In both cases, the limited range is 0.05% or more and 0.50% or less.
- both Cu and Ni are preferably 0.05% or more and 0.30% or less, respectively.
- both are preferably 0.10% or more and 0.20% or less.
- Nb 0.005% to 0.050%
- Nb is an element that improves strength and toughness without impairing corrosion resistance, and its effect is recognized from 0.005%, but when it exceeds 0.050%, the effect is saturated, so the range is 0.005% or more. It was made into 0.050% or less.
- V 0.005% to 0.050%
- Nb is an element that improves strength without impairing corrosion resistance, and an effect is observed at 0.005% or more.
- the upper limit was made 0.050%.
- Ti is an element that contributes to refinement of the crystal grain size at a high temperature through the formation of nitrides, and contributes to improvement of ductility without impairing corrosion resistance. The effect is recognized from 0.005% or more, but addition of 0.030% or more causes a large amount of carbides to precipitate, so that the ductility and toughness are hindered and processed into the gas cooking plant chimney / flue member. However, when it is used, it causes a problem of cold work cracking or a toughness failure, and is not suitable as a structural member for the gas cooking plant chimney / flue. Therefore, the range was made 0.005% or more and less than 0.030%.
- Ca 0.0005% to 0.010%
- Mg 0.0005% to 0.010%
- REM 0.001% to 0.010%
- Ca and Mg have many unclear points in steels containing Cr and Al. However, when added to steel, Ca and Mg are selectively dissolved in the environment to form an alkaline environment on the steel sheet surface, thus improving corrosion resistance. Is an element that contributes to In any case, improvement in corrosion resistance is recognized at 5 ppm or more, but when added over 100 ppm, not only the corrosion resistance improvement effect is saturated, but also the ductility and toughness of the base material tend to be reduced, The addition amount is limited to 5 ppm or more and 100 ppm or less (0.0005% or more and 0.010% or less).
- REM 0.001% to 0.010%
- ductility of the base material can be improved without impairing its corrosion resistance.
- the amount of addition needs to be 0.001% or more, but addition of a large amount inhibits it, so the upper limit is made 0.010%.
- the steel material manufacturing method of the present invention is manufactured by using a steel slab having the components described above as a starting material, through a heating process, a rolling process, and, if necessary, a heat treatment process.
- the steel slab is manufactured by a process such as a continuous casting method and an ingot-making / bundling method after the components are adjusted and melted by a converter or an electric furnace.
- Steel slabs that affect the corrosion resistance of this steel even if it is subjected to heat treatment such as quenching, tempering, or normalizing as steel sheets, shaped steel, or steel pipes by hot rolling after heating. Not.
- the chimney / flue steel of the present invention is also characterized by having an inorganic zinc rich primer layer on the surface of the base steel material having the above composition.
- the inorganic zinc rich primer layer needs to have a thickness of 5 to 100 ⁇ m. When the film thickness is less than 5 ⁇ m, it is difficult to obtain the effect of the inorganic zinc-rich primer. When the film thickness exceeds 100 ⁇ m, cracking and sagging are likely to occur, and the corrosion resistance is lowered. Furthermore, as the inorganic zinc rich primer layer becomes thicker, fume and blowholes are more likely to occur at the time of fusing and welding, and the workability decreases. In consideration of the balance of workability, corrosion resistance, and economy, the film thickness is preferably 10 to 30 ⁇ m.
- the inorganic zinc rich primer layer needs to contain 30% by mass or more of metallic zinc in the dry coating film.
- the inorganic zinc-rich primer is often composed of a silicate condensate such as an alkyl silicate ethyl silicate as a vehicle.
- the metal zinc in the heating residue is not particularly specified as long as it is 30% or more, but it is preferable in terms of reliability that it is a JIS K 5552 type 1 equivalent product.
- the formation method of the inorganic zinc rich primer layer is not particularly limited, and the inorganic zinc rich primer layer can be formed on the steel material surface by applying the inorganic zinc rich primer to the steel material with a brush or a spray. .
- a blast processing level Sa1 / 2 or more shown to ISO 8501-1 is preferable.
- spraying an inorganic zinc rich primer on the blasted steel material surface it is preferable from the point of work efficiency to spray by airless spray.
- the steel for a chimney / flue of the present invention it is possible to obtain further long-term durability by forming a heat-resistant silicone resin layer on the surface of the inorganic zinc rich primer layer.
- the thickness of the heat-resistant silicone resin layer is preferably 100 to 400 ⁇ m in consideration of the balance between corrosion resistance and economy. However, from the viewpoint of workability and weldability, it is more preferably 150 to 250 ⁇ m.
- a silicone resin paint is applied on the surface of the inorganic zinc rich primer layer by airless or air spray so that the thickness of the dry coating film becomes a desired thickness. A method of drying at room temperature and finishing. Any heat-resistant silicone-based resin coating may be used as long as it has room temperature curing, chemical resistance, and adhesion.
- steels having the alloy compositions shown in Tables 1 to 3 were melted and cast, and hot rolled to a plate thickness of 10 mm, heat-treated, and then used as test pieces.
- the said test piece was extract
- an inorganic zinc rich primer is applied to the upper layer of the test piece and dried for 7 days at room temperature and a relative humidity of 70% or less (hereinafter referred to as RH) to prepare various corrosion test pieces having an inorganic zinc rich primer layer.
- RH room temperature and a relative humidity of 70% or less
- the inorganic zinc rich primer used what was adjusted with JISK5552 1 type equivalent goods (The Nippon Steel Chemical Co., Ltd. make, brand name: NB zinc rich primer 2000NR).
- various corrosion test pieces coated with about 200 to 250 ⁇ m were prepared by airless spraying using a silicone resin (trade name: Pyrodin B # 1000, manufactured by Oshima Kogyo Co., Ltd.).
- test pieces shown in Tables 1 to 3 were subjected to natural gas-fired and liquefied petroleum gas-fired actual plant chimney / flue exposure tests, and their rust resistance, rust adhesion, and local corrosion resistance. , And their overall evaluation.
- the evaluation results are shown in Tables 4-6.
- a test piece with a 0.6 mm width X-cut inserted with a cutter to expose the surface of the steel sheet was liquefied with a natural gas-fired chimney and flue.
- the oil and gas fired plant was installed in the chimney and flue for about 3 years.
- Rust resistance was evaluated by the presence or absence of rust. That is, the case where the occurrence of red rust was not observed with the naked eye was evaluated as ⁇ (good), and the occurrence was observed as x (bad). Also, among those in which red rust was observed, a tape test method (so-called so-called rust-adhesive tape) using an adhesive tape having a nominal width of 12 mm defined in JIS Z 1522, using the peel test method in JIS H8504. And tape peeling test method). That is, a tape having rust of 10% or less in area ratio was judged as good and judged as good. The case where the area of the rust / deposits exceeds 10% was judged as defective and was evaluated as x.
- the local corrosion resistance is determined by immersing the test piece for 20 minutes in a 10% sulfuric acid aqueous solution at 50 ° C. to which 0.5% of “Hibiron” (registered trademark) manufactured by Sugimura Chemical Industry Co., Ltd. is added as an inhibitor. After completely removing the rust (in this condition, it has been confirmed that the base material does not dissolve), using a laser optical microscope, observe the 50 ⁇ 50 mm area at the center of the test surface. A portion where pitting corrosion was deep was measured, and a value of 0.03 mm / year or less was judged to be good, and the case where the corrosion rate exceeded 0.03 mm / year was judged to be bad, and was evaluated as x.
- Hibiron registered trademark manufactured by Sugimura Chemical Industry Co., Ltd.
- test pieces with a comprehensive corrosion resistance evaluation of ⁇ ⁇ '' were performed, and after the test, the occurrence of cracks / cracks on the outer surface was confirmed by visual observation, and no cracks or fine cracks were observed. ”, Those where they were recognized were evaluated as“ x ”.
- the test pieces of Examples 1 to 51 of the present invention all showed excellent results with respect to rust resistance, rust adhesion, and local corrosion resistance. Furthermore, with regard to the cold workability required as corrosion resistant steel for chimneys and flues, as shown in the results of the cold bending test, no cracks or cracks are generated on the outer surface by visual observation. It was confirmed that the material has sufficient ductility. On the other hand, the test pieces of Comparative Examples 1 to 15 did not show satisfactory results at least with respect to rust resistance and local corrosion resistance. In Comparative Examples 16 and 17, the amount of Mo or Ti was high, so that the evaluation of corrosion resistance was “ ⁇ ”, but cracks were observed in the cold bending test. From these results, the above-described findings could be confirmed, and the grounds for limitation of each steel component described above could be supported.
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- Chimneys And Flues (AREA)
Abstract
Description
近年は、天然ガス焚きまたは液化石油ガス焚きのプラントが一般的であり、煙突・煙道用構造材は普通鋼に耐熱塗装もしくはコンクリート製などが一般的である。しかしながら、コンクリート製では施工時や補修時の現場作業期間が長くなり、周辺環境への大気汚染の問題が生じている。
この飛散の問題解決について、従来、産業界からの強い要求(Long−felt need)が長い間寄せられていたが、コストに見合い、産業界を満足させる解決手段が見出されてこなかった。
なお、煙突・煙道用構造材には、煙突などに加工する際、板厚6mmで180°曲げ試験を行っても、冷間加工割れを生じないことを一つの指標とする、優れた冷間加工性が同時に要求される。
特許文献1では、鋼材の成分組成を、C:0.045%以下、Si:0.01~0.5%、Mn:0.5~2.0%、P:0.03%以下、S:0.003%以下、N:0.020%以下、Cr:11~12.5%、Ni:0.01~2.0%およびCu:0.05~2.0%を含む清掃構造用煙突で生じるSOx、NOx等の腐食環境で優れた耐食性を発揮するステンレス鋼が開示されている。
特許文献2では、SS400鋼の10倍以上の耐食性を有し、錆の生成がほとんどなく、かつ溶接性が良好なオーステナイトステンレス鋼が開示されている。
特許文献4では、5%Cr鋼をベースとして、不純物であるSを0.010%以下に低減し、さらにTiを0.005~0.05%の範囲で添加し、さらにNiを1.0~2.5%の範囲で単独添加、または0.10~1.0%の範囲で微量のCuはあるいはMoとの複合添加によって耐孔食性・耐局部腐食性とさびの密着性を飛躍的に向上させた煙突・煙道用鋼が開示されている。
さらに、特許文献7~9には、優れた溶接部靭性と同時に、結露腐食環境、大気腐食環境、水道水腐食環境、コンクリート腐食環境、海水腐食環境等の腐食環境において優れた耐食性を有する鋼として、Crを4~9%、2~7%、3~11%それぞれ含有する鋼に、Alを0.1~5%、0.1~2%、0.1~2%をそれぞれ添加した鋼の発明が開示されている。また、特許文献10に示されるように、耐硫酸露点腐食鋼として低合金鋼からの試みも提案された。
また、特許文献3の鋼材では、低コストであり、耐食性には優れているものの、現地での塗装による環境汚染の問題や、一旦塗装劣化や腐食減肉が生じると、周辺環境への錆飛散を抑制させることができない問題があり、更なる改善が求められていた。
さらに、特許文献5の鋼材では、鋼材に生成する錆層が剥がれ落ち、紛状ないし薄皮状の水酸化鉄等が煙突から外部に飛散し、環境を害することをある程度抑制できたが、その効果は十分でなく、更なる改善が産業界から求められていた。
さらに、特許文献7~9の鋼材のように、結露腐食環境、大気腐食環境において優れた耐食性を示すものでも、天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道に用いる場合、その環境下で求められる高いレベルでの耐発錆性、耐局部腐食性が必ずしも十分でないか、または、耐発錆性、耐局部腐食性が十分であっても冷間曲げ性が不十分で、天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道に用いる際の障害となることがわかった。
したがって、このようなプラントの煙突・煙道では、その特異的な腐食・使用環境の下での材料の局部腐食および錆飛散防止対策が求められていた。
また、煙突・煙道用耐食鋼として、煙突・煙道に加工するのに必要な冷間加工性の確保が求められる。
そこで、本発明は、天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道の腐食環境において、孔食等の局部腐食が進展することによる穴あきを防止し、かつ赤錆を発生させない、または、たとえ赤錆が発生しても微量であって、赤錆が地鉄との密着性を保つために錆飛散を確実に防止できる、耐発錆性、さびの密着性および耐局部腐食性(耐孔食性)に優れた、かつ、前記ガス焚きプラント煙突・煙道に用いる際に要求される冷間加工性を具備した、経済的な天然ガス焚きおよび液化石油ガス焚きのプラント煙突・煙道用耐食鋼を提供することを目的とする。
(1) 質量%で、
C:0.005%以上0.030%以下、
Si:0.18%以上0.50%以下、
Mn:1.50%以上3.00未満、
P:0.030%以下、
S:0.0050%以下、
Cr:4.0%以上9.0%以下、
Al:0.20%以上1.50%以下、
N:0.020%以下、
残部がFeおよび不可避的不純物からなることを特徴とする耐発錆性、さびの密着性および耐局部腐食性に優れた、天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。
(2) 質量%で、さらに
Cu:0.05%以上0.50%以下、
Ni:0.05%以上0.50%以下、
を含有することを特徴とする前記(1)に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。
(3) 質量%で、さらに
Mo:0.01%以上0.20%以下、
V:0.005%以上0.050%以下、
Nb:0.005%以上0.050%以下、
Ti:0.005%以上0.030%未満の何れか1種または2種以上を含有することを特徴とする前記(1)または(2)に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。
(4) 質量%で、さらに
Ca:0.0005%以上0.010%以下、
Mg:0.0005%以上0.010%以下、
REM:0.001%以上0.010%以下の何れか1種または2種以上を含有することを特徴とする前記(1)または(2)に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。
(5) さらに、その表面に、金属亜鉛分30質量%以上を含有する5~100μmの厚みの無機ジンクリッチプライマー層を有することを特徴とする前記(1)または(2)に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。
(6) 前記無機ジンクリッチプライマー層の外表面側に、20~400μmの厚みのシリコーン系樹脂層を有することを特徴とする前記(5)に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。
本発明は、前記ガス焚きプラントの煙突・煙道環境において、無機ジンクリッチプライマーを塗布することで、市販のステンレス鋼に比べて低合金の組成でありながら、経済性および耐発錆性・さびの密着性・耐局部腐食性を両立させた煙突・煙道用耐食鋼である。
具体的に、本発明の天然ガス焚きまたは液化石油ガス焚きプラントの煙突・煙道用鋼は、質量%で、C:0.005~0.030%、Si:0.18~0.50%、Mn:1.50~3.00未満、P:0.030%以下、S:0.0050%以下、Cr:4.0~9.0%、Al:0.20~1.50%、N:0.020%以下を含有し、残部がFeおよび不可避的不純物からなる組成を基本とし、さらに、性質を向上させる元素を選択的に含有させたものである。
[C:0.005%以上0.030%以下]
Cは、強度を改善する元素で0.005%以上必要であるが、0.030%を超えて添加すると、Cr系炭化物の形成により耐食性を劣化させるために、その添加量の上限を0.030%とした。なお、強度と延性、靭性、溶接性のバランスを考慮すると、0.005%以上0.020%以下が好ましい。さらに、前記バランス達成のための製造安定性を考慮すると、0.010%以上0.020%以下が好ましい。
Siは、Crを2%以上含有する鋼に脱酸剤および強化元素として添加することが有効であるが、含有量が0.18%未満ではその脱酸効果が十分でなく、その結果、溶存酸素とAlが酸化物を生成し易くなり、後述のように不働態皮膜の安定性を向上させるために有効な固溶Al量を十分に確保できなくなる。一方、0.50%を超えて含有するとその効果は飽和し、靭性を低下させうるので、含有量の範囲を0.18%以上0.50%以下に限定する。さらに鋼材の製造性、溶接性を考慮した場合、0.20%以上0.30%以下が好ましい。
Crは、後述のAlとともに、不働態皮膜の安定性を向上させることにより、耐食性を確保するために4.0%以上を含有することが必要であるが、9.0%を超えて含有させてもコストを増すばかりか、母材の靭性を損なうので上限の含有量は9.0%とする。なお、鋼材の製造性、溶接性、加工性を考慮すると、5.5%以上7.5%以下が好ましい。さらに、コストとのバランスを考慮すると、5.8%以上6.3%以下が好ましい。
Alは、本発明において、不働態皮膜の安定性を向上させることにより、耐食性を確保するためにCrと並んで重要な元素である。Alの含有量は、不働態皮膜の安定性を向上させる固溶Al量を確保する観点から0.20%以上必要であるが、一方、1.50%を越えて添加すると、フェライト相変態の温度範囲が極めて広くなり製造過程での鋳片割れなどの原因となるので、その含有量は0.20%以上1.50%以下に限定する。さらに、加工性を考慮すると、0.50%以上1.30%以下が好ましい。さらに、耐食性、製造性および、コストとのバランスを考慮すると、0.85%以上1.20%以下が好ましい。
Mnは、本発明においては、主として、強度を確保するために、また、オーステナイト形成元素として作用して、耐食性の観点から添加されているCrおよびAlにより助長される粗大フェライトの形成を抑制するために添加される。すなわち、CrおよびAlは、周知のようにフェライト形成元素であり、これらが多量に添加されると、凝固から室温に至るまで変態を経ずしてフェライト単相組織となり、鋳片割れなどが生じ、製造性が低下する。
したがって、このような効果を得るために、Mnは1.50%以上添加することが必要であるが、3.00%以上の添加では母材の延性が著しく低下するため3.00%未満の添加とする。なお、鋼材の強度、製造性、溶接性、加工性を考慮すると、2.00%以上3.00%未満が好ましい。
Nは、鋼板の多量に添加されると窒化物の形成などで母材の延性や耐食性を阻害するために、上限は0.020%とする。
[P:0.030%以下]
Pは、鋼中に不純物として存在するが、延性を低下し、製造性を低下させるのですくない方が望ましく、上限の含有量は0.030%とした。さらに、製造性、コストの観点から、好ましくは0.020%以下である。
[S:0.0050%以下]
Sは、多量に添加すると耐孔食性・耐局部腐食性を低下させるので少ない方が望ましく、上限の含有量は0.0050%とする。なお、SとPは、不可避的な不純物であり、可能な限り少なくするほうがよい。
加えて、Mo:0.01%以上0.20%以下、V:0.005%以上0.050%以下、Nb:0.005%以上0.050%以下、Ti:0.005%以上0.030%未満の何れか1種または2種以上を含有させることで、更に耐発錆性・耐孔食性および耐局部腐食性を向上させる、もしくは耐食性に影響を及ぼさずに強度、靭性を向上させることが可能である。
[Ni:0.05%以上0.50%以下]
Cu、Niは、ともに前記ガス焚きプラントの排ガス環境における、耐発錆性・耐孔食性および耐局部腐食性を向上させる元素であり、添加する場合はともに添加される。
Cuは、Niに比べて発錆および局部腐食を抑える効果が大きい。しかし、Cuは偏析し易い面がある。特に、鋳造組織のデンドライト(Dendrite)間の凝固偏析に由来する局部的なCuの偏析部が、製品表面で残存する場合がある。製品表面でこのような偏析部があれば、前記ガス焚きプラントの排ガス環境における高濃度炭酸ガス雰囲気の凝縮水存在下では、かかる偏析部とその周囲との間に電位差を生じて、電位が低くなった部位が局部腐食または発錆の起点となりうる。
ところが、Niを同時に添加すれば、NiはCuの偏析を軽減する作用があり、両方添加するとその相乗効果が発現する。
Cu、Niは、これらの効果の発現のためには、いずれも0.05%以上の添加を必要とするが、いずれも0.50%を越えて添加されると脆化が生じるために、両者ともに、その限定範囲を0.05%以上0.50%以下とする。さらに、安定的な製造性の観点から好ましくは、Cu、Niともにそれぞれ、0.05%以上0.30%以下である。さらに、コストとのバランスを考慮すると、両者ともに、0.10%以上0.20%以下が好ましい。
Moは、CrおよびAlが添加された鋼において、0.01%以上添加されると、母材の特性を損なうことなく孔食の発生と成長を抑制する効果が認められる。しかし、0.20%を終えて添加しても効果が飽和するばかりか母材の延性および靭性を低下させる。そのため、前記ガス炊きプラントの煙突・煙道用部材に加工する際、冷間加工割れ、表面微細割れを生じ、煙突・煙道の構造用部材として適さなくなるので、その範囲を0.01%以上0.20%以下とした。
Nbは、耐食性を損なわずに、強度および靭性を改善する元素であり、その効果は0.005%から認められるが、0.050%を越えると効果が飽和するので範囲を0.005%以上0.050%以下とした。
Vは、Nbと同じく耐食性を損なわずに強度を改善する元素であり、0.005%以上で効果が認められるが、多量の添加は延性を阻害するので上限を0.050%とした。
Tiは、窒化物の生成を通じて高温での結晶粒径の細粒化に寄与する元素であり、耐食性を損なわずに、延性の改善などに寄与する。その効果は0.005%以上から認められるが、0.030%以上の添加では炭化物が多量に析出するために、かえって延性および靭性を阻害し、前記ガス炊きプラント煙突・煙道用部材に加工し使用する際、冷間加工割れを生じる場合または靭性低下の不具合を生じ、前記ガス炊きプラント煙突・煙道の構造用部材として適さない。したがって、その範囲を0.005%%以上0.030%未満とした。
[Mg:0.0005%以上0.010%以下]
CaおよびMgは、CrおよびAlを含有する鋼において、不明な点は多いが、鋼中に添加することで、環境中で選択的に溶解し、鋼板表面でアルカリ環境を形成することから耐食性向上に寄与する元素である。いずれも5ppm以上で耐食性の向上は認められるが、100ppmを越えて添加すると、耐食性向上効果が飽和するばかりでなく、母材の延性や靭性が低下する傾向が明きからとなっており、その添加量を5ppm以上100ppm以下(0.0005%以上0.010%以下)に限定する。
本発明では、希土類元素(REM)を適宜添加しても、その耐食性を損なわずに、母材の延性などを改善することが可能である。その添加量は、0.001%以上を必要とするが、多量の添加はそれを阻害するので、その上限を0.010%とする。
本発明の煙突・煙道用鋼は、上記組成からなる下地鋼材の表面に、無機ジンクリッチプライマー層を有することも特徴としている。
無機ジンクリッチプライマー層は、その膜厚を5~100μmとする必要がある。膜厚が5μm未満では無機ジンクリッチプライマーの効果が得られ難く、また100μmを超えると、割れやダレを生じやすくなり、耐食性が低下する。さらに、無機ジンクリッチプライマー層は、膜厚が厚くなればなるほど、溶断・溶接時にヒュームやブローホールを生じやすくなり、加工性が低下する。また、加工性、耐食性、経済性のバランスを考慮すると、膜厚は10~30μmが好ましい。
耐熱性のシリコーン系樹脂層の厚みは、耐食性、経済性のバランスを考慮すると、100~400μmとすることが好ましい。但し、施工性、溶接性の観点から150~250μmとすることがより好ましい。
耐熱性のシリコーン系樹脂層の施工方法としては、無機ジンクリッチプライマー層の表面に、エアレスまたはエアスプレー等により、乾燥塗膜の厚さが所望の厚みになるよう、シリコーン系樹脂塗料を塗装し、常温で乾燥させて仕上げる方法があげられる。耐熱性のシリコーン系樹脂塗料としては常温硬化性・耐薬品性・密着性を有するものであれば良い。
また、シリコーン系樹脂(大島工業株式会社製、商品名:パイロジンB#1000)を用い、エアレススプレーで、200~250μm程度塗布した各種腐食試験片を準備した。
なお、実プラント暴露試験は、不可避的な欠陥を模擬するために、幅0.6mmのXカットをカッターで入れて地鉄面を露出させた試験片を、天然ガス焚き煙突・煙道内と液化石油ガス焚きプラント煙突・煙道内に約3年間設置することにより実施した。
また、赤錆が認められたもののうち、さびの密着性をJIS H 8504における、引きはがし試験方法を流用し、JIS Z 1522に規定された呼び幅12mmの粘着テープを用いた、テープ試験方法(いわゆる、テープ剥離試験方法)で評価した。すなわち、テープにさびが面積率で10%以下のものを密着性良好と判断し○とした。さび・付着物の面積が10%を越えるものを不良と判断し×とした。
さらに、鋼材を天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道に冷間加工する際に、必要な延性を備えていることを確認するために、耐食性総合評価が「○」の試験片について、各板厚6mm材の180°冷間曲げ試験を行い、試験後、外側表面の割れ・亀裂の発生状況を目視観察で確認し、割れや微細な亀裂の発生が認められないものを「○」、それらが認められたものを「×」と評価した。
一方、比較例1~15の試験片は、少なくとも耐発錆性および耐局部腐食性について満足できる結果を示さなかった。さらに、比較例16、17は、MoまたはTiの量が高いので、耐食性の評価では「○」であったが、冷間曲げ試験では亀裂の発生が認められた。
これらの結果から、上述した知見を確認することができ、また、上述した各鋼成分の限定の根拠を裏付けることができた。
Claims (6)
- 質量%で、
C:0.005%以上0.030%以下、
Si:0.18%以上0.50%以下、
Mn:1.50%以上3.00未満、
P:0.030%以下、
S:0.0050%以下、
Cr:4.0%以上9.0%以下、
Al:0.20%以上1.50%以下、
N:0.020%以下を含有し、
残部がFeおよび不可避的不純物からなることを特徴とする耐発錆性、さびの密着性および耐局部腐食性に優れた、天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。 - 質量%で、さらに
Cu:0.05%以上0.50%以下、
Ni:0.05%以上0.50%以下、
を含有することを特徴とする請求項1に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。 - 質量%で、さらに
Mo:0.01%以上0.20%以下、
V:0.005%以上0.050%以下、
Nb:0.005%以上0.050%以下、
Ti:0.005%以上0.030%未満の何れか1種または2種以上を含有することを特徴とする請求項1または2に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。 - 質量%で、さらに
Ca:0.0005%以上0.010%以下、
Mg:0.0005%以上0.010%以下、
REM:0.001%以上0.010%以下の何れか1種または2種以上を含有することを特徴とする請求項1または2に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。 - さらに、その表面に、金属亜鉛分30質量%以上を含有する5~100μmの厚みの無機ジンクリッチプライマー層を有することを特徴とする請求項1または2に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。
- 前記無機ジンクリッチプライマー層の外表面側に、20~400μmの厚みのシリコーン系樹脂層を有することを特徴とする請求項5に記載の天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼。
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2010800020965A CN102099502A (zh) | 2009-03-30 | 2010-03-19 | 天然气焚烧或者液化石油气焚烧设备烟囱或烟道用耐蚀钢 |
| JP2010529585A JP4644316B2 (ja) | 2009-03-30 | 2010-03-19 | 天然ガス焚きまたは液化石油ガス焚きプラント煙突・煙道用耐食鋼 |
| US12/998,559 US20110217566A1 (en) | 2009-03-30 | 2010-03-19 | Corrosion-resistant steel for chimney/flue use in natural gas-fired or liquefied petroleum gas-fired plants |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009082278 | 2009-03-30 | ||
| JP2009-082278 | 2009-03-30 |
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| Publication Number | Publication Date |
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| WO2010113828A1 true WO2010113828A1 (ja) | 2010-10-07 |
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| Country | Link |
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| US (1) | US20110217566A1 (ja) |
| JP (1) | JP4644316B2 (ja) |
| KR (1) | KR20110018445A (ja) |
| CN (1) | CN102099502A (ja) |
| WO (1) | WO2010113828A1 (ja) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012092437A (ja) * | 2010-09-30 | 2012-05-17 | Nippon Steel Corp | 揚貯運炭設備用耐食鋼材、揚貯運炭設備用部材及び耐食鋼材の使用方法 |
| JP2016089246A (ja) * | 2014-11-10 | 2016-05-23 | 新日鐵住金株式会社 | 耐食鋼材 |
| JP2019116648A (ja) * | 2017-12-26 | 2019-07-18 | 日本製鉄株式会社 | 鋼材 |
| JP2022543573A (ja) * | 2019-07-31 | 2022-10-13 | ポスコ | 耐食性に優れた排気系用フェライト系鋼板 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113072878A (zh) * | 2021-03-29 | 2021-07-06 | 浙江大江节能科技有限公司 | 一种余热锅炉烟道内壁防腐蚀涂料及其施工方法 |
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| JP2004115912A (ja) * | 2002-09-06 | 2004-04-15 | Jfe Steel Kk | 自動車足回り用Fe−Cr系合金 |
| JP2004162119A (ja) * | 2002-11-13 | 2004-06-10 | Nippon Steel Corp | 溶接熱影響部靭性に優れた耐食鋼 |
| JP2004277839A (ja) * | 2003-03-18 | 2004-10-07 | Nippon Steel Corp | 亜鉛系金属被覆鋼材 |
| JP2008127653A (ja) * | 2006-11-22 | 2008-06-05 | Nippon Steel Corp | 裸耐発錆性に優れた耐食鋼材 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS58133871A (ja) * | 1982-02-05 | 1983-08-09 | Asahi Glass Co Ltd | 防食被覆方法 |
| JP4441295B2 (ja) * | 2004-03-15 | 2010-03-31 | 新日本製鐵株式会社 | 耐食性および切削性に優れた溶接用高強度鋼および溶接用高強度鋼板の製造法 |
| WO2007097142A1 (ja) * | 2006-02-27 | 2007-08-30 | Jfe Steel Corporation | 船舶用耐食鋼材 |
-
2010
- 2010-03-19 CN CN2010800020965A patent/CN102099502A/zh active Pending
- 2010-03-19 WO PCT/JP2010/055482 patent/WO2010113828A1/ja not_active Ceased
- 2010-03-19 JP JP2010529585A patent/JP4644316B2/ja active Active
- 2010-03-19 US US12/998,559 patent/US20110217566A1/en not_active Abandoned
- 2010-03-19 KR KR1020117000985A patent/KR20110018445A/ko not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004115912A (ja) * | 2002-09-06 | 2004-04-15 | Jfe Steel Kk | 自動車足回り用Fe−Cr系合金 |
| JP2004162119A (ja) * | 2002-11-13 | 2004-06-10 | Nippon Steel Corp | 溶接熱影響部靭性に優れた耐食鋼 |
| JP2004277839A (ja) * | 2003-03-18 | 2004-10-07 | Nippon Steel Corp | 亜鉛系金属被覆鋼材 |
| JP2008127653A (ja) * | 2006-11-22 | 2008-06-05 | Nippon Steel Corp | 裸耐発錆性に優れた耐食鋼材 |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012092437A (ja) * | 2010-09-30 | 2012-05-17 | Nippon Steel Corp | 揚貯運炭設備用耐食鋼材、揚貯運炭設備用部材及び耐食鋼材の使用方法 |
| JP2016089246A (ja) * | 2014-11-10 | 2016-05-23 | 新日鐵住金株式会社 | 耐食鋼材 |
| JP2019116648A (ja) * | 2017-12-26 | 2019-07-18 | 日本製鉄株式会社 | 鋼材 |
| JP6992499B2 (ja) | 2017-12-26 | 2022-01-13 | 日本製鉄株式会社 | 鋼材 |
| JP2022543573A (ja) * | 2019-07-31 | 2022-10-13 | ポスコ | 耐食性に優れた排気系用フェライト系鋼板 |
| JP7297373B2 (ja) | 2019-07-31 | 2023-06-26 | ポスコ カンパニー リミテッド | 耐食性に優れた排気系用フェライト系鋼板 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPWO2010113828A1 (ja) | 2012-10-11 |
| KR20110018445A (ko) | 2011-02-23 |
| CN102099502A (zh) | 2011-06-15 |
| JP4644316B2 (ja) | 2011-03-02 |
| US20110217566A1 (en) | 2011-09-08 |
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