EP1990437A1 - Corrosion-resistant steel material for ship and vessel - Google Patents

Corrosion-resistant steel material for ship and vessel Download PDF

Info

Publication number
EP1990437A1
EP1990437A1 EP07707040A EP07707040A EP1990437A1 EP 1990437 A1 EP1990437 A1 EP 1990437A1 EP 07707040 A EP07707040 A EP 07707040A EP 07707040 A EP07707040 A EP 07707040A EP 1990437 A1 EP1990437 A1 EP 1990437A1
Authority
EP
European Patent Office
Prior art keywords
mass
steel
corrosion
paint film
corrosion resistance
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
Application number
EP07707040A
Other languages
German (de)
French (fr)
Other versions
EP1990437A4 (en
EP1990437B1 (en
Inventor
Kazuhiko Shiotani
Tsutomu Komori
Toshiyuki Hoshino
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Steel Corp
Original Assignee
JFE Steel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by JFE Steel Corp filed Critical JFE Steel Corp
Publication of EP1990437A1 publication Critical patent/EP1990437A1/en
Publication of EP1990437A4 publication Critical patent/EP1990437A4/en
Application granted granted Critical
Publication of EP1990437B1 publication Critical patent/EP1990437B1/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B63—SHIPS OR OTHER WATERBORNE VESSELS; RELATED EQUIPMENT
    • B63B—SHIPS OR OTHER WATERBORNE VESSELS; EQUIPMENT FOR SHIPPING 
    • B63B3/00—Hulls characterised by their structure or component parts
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D7/00—Modifying the physical properties of iron or steel by deformation
    • C21D7/02—Modifying the physical properties of iron or steel by deformation by cold working
    • C21D7/04—Modifying the physical properties of iron or steel by deformation by cold working of the surface
    • C21D7/06—Modifying the physical properties of iron or steel by deformation by cold working of the surface by shot-peening or the like
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0205—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips of ferrous alloys
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/06—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of rods or wires
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • 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
    • C22C38/008—Ferrous alloys, e.g. steel alloys containing tin
    • 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
    • C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
    • 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
    • C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
    • 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
    • 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
    • C22C38/60—Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
    • C—CHEMISTRY; METALLURGY
    • C21—METALLURGY OF IRON
    • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226—Hot rolling

Definitions

  • the present invention relates to anti-corrosion steel used for ships such as a coal ship, an ore carrier, an ore coal carrier, a crude oil tanker, an LPG carrier, an LNG carrier, a chemical tanker, a container ship, a bulk carrier, a log carrier, a chip carrier, a refrigerated cargo ship, a pure car carrier, a heavy load carrier, a roll-on/roll-off ship, a limestone carrier, and a cement carrier, and particularly relates to anti-corrosion steel for ship used for a ballast tank and the like under a severe corrosion environment with seawater.
  • the anti-corrosion steel for ship described in the invention includes a thick steel plate, sheet steel, shape sheet, and bar steel.
  • ballast tank of a ship serves to enable stable navigation of a ship by being poured with seawater while no cargo is loaded, the tank is placed in an extremely severe corrosion environment. Therefore, an anti-corrosion paint film using epoxy paint is formed, in addition, cathodic protection is applied for preventing corrosion of steel used for the ballast tank.
  • Life of an anti-corrosion paint film of a ballast tank is said to be typically about 10 years under such a drastic corrosion resistance, that is, half the life (20 years) of a ship. It is actual situation that corrosion resistance is kept by performing repair painting in the remaining ten years. However, since the ballast tank is in the severe corrosion environment as above, even if the repair painting is carried out, an effect of the painting is hard to be kept for a long time. Moreover, since the repair painting is performed as operation in a narrow space, operation environment is not preferable. Thus, it is desirable to develop a steel material having an excellent corrosion resistance, which can lengthen a period before the repair painting to the utmost, and can reduce an operation load of the repair painting to the utmost.
  • patent document 1 discloses anti-corrosion low alloy steel including steel containing C of 0.20 mass% or less, the steel being added with Cu of 0.05 to 0.50 mass% and W of 0.01 to less than 0. 05 mass% as elements that improves corrosion resistance, and furthermore added with one or at least two of Ge, Sn, Pb, As, Sb, Bi, Te and Be in a range of 0.01 to 0.2 mass% as the elements.
  • Patent document 2 discloses anti-corrosion low alloy steel including steel containing C of 0.20 mass% or less, the steel being added with Cu of 0.05 to 0.50 mass% and W of 0. 05 to 0.
  • Patent document 3 discloses anti-corrosion low alloy steel including steel containing C of 0.15 mass% or less, which is added with Cu of 0.05 to less than 0.15 mass% and W of 0.05 to 0.5 mass%.
  • Patent document 4 discloses a ballast tank in which anti-corrosion low alloy steel, which includes steel containing C of 0.15 mass% or less, the steel being added with P of 0.03 to 0.10 mass%, Cu of 0.1 to 1.0 mass%, and Ni of 0.1 to 1.0 mass% as elements that improve corrosion resistance, is coated with anti-corrosion paint such as tar epoxy paint, pure epoxy paint, epoxy paint without solvent, and urethane paint, and then covered with resin.
  • This technology is intended to lengthen the life of anti-corrosion painting by improving corrosion resistance of steel itself, and thereby achieve a ship being free from maintenance over 20 to 30 years corresponding to the useful life of a ship.
  • Patent document 5 makes a proposal that steel containing C of 0.15 mass% or less is added with Cr of 0.2 to 5 mass% as an element that improves corrosion resistance in order to achieve a ship being free from maintenance. Furthermore, patent document 6 proposes an anti-corrosion method of a ballast tank characterized in that steel containing C of 0.15 mass% or less, which is added with Cr of 0.2 to 5 mass% as an element that improves corrosion resistance, is used as a componential material, and oxygen gas concentration within a ballast tank has a value in a ratio of 0.5 or less with respect to a value of oxygen gas concentration in air.
  • Patent document 7 makes a proposal that steel containing C of 0.1 mass% or less is added with Cr of 0.5 to 3.5 mass% to improve corrosion resistance, so that a ship being free from maintenance is achieved. Furthermore, patent document 8 discloses steel for ship in which steel containing C of 0.001 to 0.025 mass% is added with Ni of 0.1 to 4.0 mass% to improve paint-film damage resistance, so that maintenance cost for repair painting and the like is reduced.
  • Patent document 9 discloses steel for ship in which steel containing C of 0.01 to 0.25 mass% is added with Cu of 0.01 to 2.00 mass% and Mg of 0.0002 to 0.0150 mass% so as to have corrosion resistance in use environment such as a shell of a ship, a ballast tank, a cargo oil tank, and an iron-ore cargo hold. Furthermore, patent document 10 discloses steel in which steel containing C of 0.001 to 0.2 mass% is compositely added with Mo, W and Cu, and limited in the added amount of P and S as impurities, thereby general corrosion or local corrosion that may occur in a crude oil tank is inhibited.
  • each of the patent documents 1 to 3 does not make adequate investigation on corrosion resistance under presence of a paint film of Zinc-primer or epoxy paint being typically coated on steel configuring a ballast tank or the like. Therefore, further investigation is necessary for improving corrosion resistance under presence of the paint film.
  • the steel described in the patent document 4 is added with a comparatively large amount of P, 0.03 to 0.10 mass%, to improve corrosion resistance of base metal, which is problematic in a point of weldability and toughness of a weld.
  • the steel described in each of the patent documents 5 and 6 is added with a comparatively large amount of Cr, 0.2 to 5 mass%.
  • the steel described in the patent document 7 is added with a comparatively large amount of Cr, 0.5 to 3.5 mass%. Either of them is problematic in the point of weldability and toughness of a weld, in addition, problematic in that manufacturing cost is increased.
  • the steel described in the patent document 8 is comparatively low in C content, and comparatively high in Ni content, which is problematic in that manufacturing cost is increased.
  • the steel described in the patent document 9 is problematic in that Mg is essentially added, which causes unstableness in yield of steel manufacture, leading to unstableness in mechanical properties of the steel.
  • the steel described in the patent document 10 is anti-corrosion steel used in the crude oil tank, namely, used under an environment having H 2 S, and therefore the steel is unclear in corrosion resistance in the ballast tank having no H 2 S.
  • corrosion resistance has not been investigated in a condition that zinc-primer being typically used for steel for a ballast tank is coated, further investigation on corrosion resistance is necessary to be used for a ballast tank.
  • a ship is built by welding steel materials such as a thick steel plate, sheet steel, shape steel, and bar steel, and surfaces of the steel materials are applied with anti-corrosion painting before use.
  • the anti-corrosion painting is typically applied in a manner that zinc-primer is coated for primary rust prevention, and epoxy paint is coated as secondary painting (main painting) after subassembly or main assembly is performed. Therefore, the major part of steel surface of a ship has a double-layer structure thereon, which includes a zinc primer paint film and an epoxy paint film.
  • zinc primer is repainted on the weld as touch up paint for rust prevention in a period after welding and before main painting.
  • an object of the invention is to provide anti-corrosion steel for ship at low cost, which exhibits excellent corrosion resistance without depending on a surface condition of steel even under a severe corrosion environment such as a ballast tank of a ship, whereby a period before repair painting can be lengthened, consequently operation load of the repair painting can be reduced.
  • the inventors made earnest study for developing the steel that exhibits excellent corrosion resistance without depending on the surface condition of the steel even under the severe corrosion environment caused by seawater.
  • W and Cr are contained as essential elements, in addition, elements that improve corrosion resistance such as Sb and Sn are contained in an appropriate range, thereby the steel that exhibits excellent corrosion resistance can be obtained in any of the conditions of the double-layer structure of a zinc primer paint film and an epoxy paint film, only an epoxy paint film, and bare steel, and consequently they completed the invention.
  • the invention includes anti-corrosion steel for ship containing C of 0.03 to 0.25 mass%, Si of 0.05 to 0.50 mass%, Mn of 0.1 to 2.0 mass%, P of 0.025 mass% or less, S of 0.01 mass% or less, Al of 0.005 to 0.10 mass%, W of 0.01 to 1.0 mass%, Cr of 0.01 mass% or more and less than 0.20 mass%, N of 0.001 to 0.008 mass%, and the remainder including Fe and inevitable impurities.
  • the steel of the invention is characterized by containing a component in at least one group between the following groups A and B, in addition to the above composition.
  • Group A one or two selected from Sb of 0. 001 to 0. 3 mass% and Sn of 0.001 to 0.3 mass%.
  • Group B one or at least two selected from Ni of 0.005 to 0.25 mass%, Mo of 0.01 to 0.5 mass%, and Co of 0.01 to 1.0 mass.
  • the steel of the invention is characterized by containing a component in at least one group among the following groups C to E, in addition to the above composition.
  • Group C one or at least two selected from Nb of 0.001 to 0.1 mass%, Ti of 0. 001 to 0.1 mass%, Zr of 0. 001 to 0.1 mass%, and V of 0.002 to 0.2 mass%.
  • Group E one or at least two selected from Ca of 0.0002 to 0.01 mass%, REM of 0.0002 to 0.015 mass%, and Y of 0.0001 to 0.1 mass%.
  • steel of the invention is characterized in that an epoxy paint film or a zinc primer paint film is formed on a surface of the steel, or both the zinc primer paint film and the epoxy paint film are formed thereon.
  • steel can be provided, the steel having excellent corrosion resistance even under a severe corrosion environment caused by seawater, which significantly contributes to lengthening of a period before repair painting, and reduction in operation load of repair painting.
  • the inventors conducted the following experiment to develop steel having excellent corrosion resistance in any of the three portions that may exist on a surface of steel of a ship in service, that is, a portion of the double-layer structure of a zinc primer paint film and an epoxy paint film, a portion of only an epoxy paint film, and a bare steel portion.
  • test pieces 5 mm thick, 100 mm wide, and 200 mm long, and test pieces 5 mm thick, 50 mm wide, and 150 mm long were taken from the hot-rolled plates. Then, a surface of each of the test pieces was subjected to shot blasting to remove scales or oil from the surface, and then the test pieces were subjected to the following three types of surface treatment, so that exposure test pieces were prepared.
  • a double-layer film of a zinc primer film (about 15 ⁇ m) and a tar epoxy resin paint film (about 100 ⁇ m) is formed on a surface of a test piece.
  • Condition B A single-layer film of a tar epoxy resin paint film (about 100 ⁇ m) is formed on a surface of a test piece.
  • Condition C A surface of a test piece is subjected to shot blasting and remains bare (with no anti-corrosion film).
  • test pieces were subjected to a salt-spray alternate-drying-and-wetting corrosion test, which simulates a corrosion environment corresponding to a back of an upper deck of a ballast tank of an actual ship, based on a condition that an exposure test was performed by 132 cycles, each cycle including spraying of 5% NaCl solution at 35°C for 2 hr, leaving to stand at 60°C and RH25% for 4 hr, and leaving to stand at 50°C and RH95% for 2 hr, thereby the test pieces were evaluated in corrosion resistance.
  • a salt-spray alternate-drying-and-wetting corrosion test which simulates a corrosion environment corresponding to a back of an upper deck of a ballast tank of an actual ship, based on a condition that an exposure test was performed by 132 cycles, each cycle including spraying of 5% NaCl solution at 35°C for 2 hr, leaving to stand at 60°C and RH25% for 4 hr, and leaving to stand at 50°C
  • each test piece having a paint film corrosion resistance was evaluated in a way that a scratch in 80 mm in length, which reached a surface of base steel, was formed in a straight line by a box cutter through the paint film before the test, and area of a swollen paint film generated around the scratch was measured for evaluation after the test.
  • corrosion resistance was evaluated in a way that the test pieces were derusted after the test, and the average amount of decrease in thickness was calculated for evaluation from the amount of change in weight (amount of decrease) between the derusted test piece and a test piece before the test.
  • the invention was designed to use a componential system in which W and Cr were compositely contained as essential elements for improving corrosion resistance. Furthermore, the invention was designed in a way that when more excellent corrosion resistance was required, a component design was used, in which one or two selected from Sb and Sn were contained in addition to W and Cr. Moreover, the invention was designed in a way that when further more excellent corrosion resistance was required, one or two or more selected from Ni, Mo and Co were additionally contained.
  • C is an effective element for increasing strength of steel, and needs to be contained by 0.03 mass% or more to obtain a desired strength in the invention.
  • toughness of HAZ welding heat-affected zone
  • C is contained in a range of 0.03 to 0.25 mass%.
  • C is preferably contained in a range of 0.05 to 0.20 mass%.
  • Si 0.05 to 0.50 mass%
  • Si is an element to be added as a deoxidizer, or added for increasing strength of steel, and contained by 0.05 mass% or more in the invention. However, when Si is added by more than 0.50 mass%, toughness of steel is degraded, therefore an upper limit of Si is specified to be 0.50 mass%.
  • Mn 0.1 to 2.0 mass%
  • Mn is an element having an effect of preventing hot shortness, and increasing strength of steel, and added by 0.1 mass% or more. However, when Mn is added by more than 2.0 mass%, toughness of steel and weldability are reduced, therefore Mn is contained to be 2.0 mass% or less. Preferably, Mn is contained in a range of 0.5 to 1.6 mass%. P: 0.025 mass% or less
  • P is a harmful element that may degrade toughness of steel as mother material, and furthermore degrade weldability and toughness of a weld, and therefore P is preferably reduced to the utmost.
  • P is contained to be 0.025 mass% or less.
  • P is contained to be 0.014 mass% or less. S: 0.01 mass% or less
  • S is a harmful element that may degrade toughness of steel and weldability
  • S is preferably reduced to the utmost, and contained to be 0.01 mass% or less in the invention.
  • Al is an element to be added as a deoxidizer, and added by 0.005 mass% or more. However, when Al is contained by more than 0.10 mass%, Al 3+ eluted due to corrosion of base steel reduces pH of a surface of the base steel, leading to degradation in corrosion resistance, therefore an upper limit of Al is specified to be 0.10 mass%. W: 0.01 to 1.0 mass%
  • W improves corrosion resistance under presence of both the zinc primer paint film and the epoxy paint film, and significantly improves corrosion resistance under presence of only the epoxy paint film. Moreover, W significantly improves corrosion resistance of steel even if the steel is bare. Therefore, W is one of the most important elements for improving corrosion resistance in the steel of the invention.
  • the effect is exhibited in W content of 0.01 mass% or more. However, when W content is more than 1.0 mass%, the effect is saturated. Accordingly, the content of W is in a range of 0.01 to 1. 0 mass%.
  • W has the effect of improving corrosion resistance
  • WO 4 2- is produced in produced rust
  • presence of the WO 4 2- prevents chloride ions from entering a steel plate surface
  • furthermore sparingly-soluble FeWO 4 is produced in a region having decreased pH such as an anode area of the steel plate surface
  • presence of the FeWO 4 also prevents chloride ions from entering the steel plate surface.
  • the chloride ions are thus prevented from entering the steel plate surface, thereby corrosion of the steel plate is effectively inhibited.
  • inhibitor operation of WO 4 2- also inhibits corrosion of steel.
  • Cr 0.01 mass% or more and less than 0.20 mass%
  • Cr Since Cr exhibits excellent corrosion resistance under presence of both the zinc primer paint film and the epoxy paint film, Cr is one of the important elements in the steel of the invention. It is presumed that under presence of zinc primer, Zn in the zinc primer is eluted, so that Zn-based corrosion products such as ZnO and ZnCl 2 •4Zn(OH) 2 are produced, and Cr acts on the Zn-based corrosion products so as to further improve corrosion prevention of base steel given by the Zn-based corrosion products. Such a corrosion resistance improvement effect of Cr under presence of the zinc primer is exhibited at the content of Cr of 0.01 mass% or more. However, when Cr is contained by 0.20 mass% or more, toughness of a weld is degraded. Accordingly, the content of Cr is in a range of 0.01 mass% or more and less than 0.20 mass%. N: 0.001 to 0.008 mass%
  • N is a harmful component for toughness, and desirably reduced to the utmost in order to achieve improvement in toughness.
  • N is industrially hard to be decreased to less than 0.001 mass%.
  • toughness is significantly degraded. Accordingly, the content of N is in a range of 0.001 to 0.008 mass% in the invention.
  • the steel of the invention may contain the following components in addition to the above components for the purpose of further improving corrosion resistance.
  • Sb has an effect of improving corrosion resistance under presence of both the zinc primer paint film and the epoxy paint film, under presence of only the epoxy paint film, and in a condition of bare steel.
  • Sn has an effect of improving corrosion resistance under presence of only the epoxy paint film, and in the condition of bare steel.
  • the reason for the effects of Sb and Sn is considered to be that corrosion is inhibited in a region having decreased pH such as an anode area of the steel plate surface. While the effects are exhibited when either of Sn and Sb is contained by 0.001 mass% or more, in the case that the content is more than 0.3 mass%, toughness of each of mother material and HAZ is degraded, therefore each of Sn and Sb is preferably contained in a range of 0.001 to 0.3 mass%.
  • Ni, Mo and Co slightly improve corrosion resistance under presence of both the zinc primer paint film and the epoxy paint film, and in the condition of bare steel. Furthermore, Mo slightly improves corrosion resistance even under presence of only the epoxy paint film. Therefore, when corrosion resistance is desired to be further improved, the elements may be supplementarily contained.
  • the reason for the effects of Ni, Mo and Co is considered to be that they act to refine rust particles, in addition, Mo produces MoO 4 2- in rust and thus prevents chloride ions from entering a steel plate surface. The effects are exhibited in the Ni content of 0.005 mass% or more, Mo content of 0.01 mass% or more, and Co content of 0.01 mass% or more respectively.
  • Ni, Mo and Co are preferably contained in the above range respectively.
  • the steel of the invention may contain the following components in addition to the above components for increasing strength of steel and/or improving toughness.
  • Nb, Ti, Zr and V is an element that improves strength of steel, and can be selectively contained depending on required strength.
  • each of Nb, Ti and Zr is contained by 0.001 mass% or more, and V is contained by.0.002 mass% or more.
  • Nb, Ti or Zr is added by more than 0.1 mass%, and when V is added by more than 0.2 mass%, toughness is reduced, therefore each of Nb, Ti, Zr and V is preferably added with each of the above values being specified as an upper limit value.
  • B 0.0002 to 0.003 mass%
  • B is an element that improves strength of steel, and can be contained as needed. To obtain the effect, B is preferably contained by 0.0002 mass% or more. However, when B is added by more than 0.003 mass%, toughness is degraded. Accordingly, B is preferably contained in a range of 0.0002 to 0.003 mass%. One or at least two of 0.0002 to 0.01 mass% Ca, 0.0002 to 0.015 mass% REM, and 0.0001 to 0.1 mass% Y
  • any of Ca, REM and Y is an element having an effect of improving toughness of a weld heat-affected zone, and can be selectively contained as needed. While such an effect is obtained in the content of Ca of 0.0002 mass% or more, REM of 0. 0002 mass% or more, and Y of 0.0001 mass% or more respectively, when Ca of more than 0.01 mass%, REM of more than 0.015 mass%, and Y of more than 0.1 mass% are added respectively, toughness is rather reduced, therefore Ca, REM and Y are preferably contained with the above values being specified as upper limit values respectively.
  • the steel of the invention preferably contains Fe and inevitable impurities as components other than the above.
  • the invention is not intended to reject to contain a component other than the above if an effect of the component is within a level at which it does not kill the effect of the invention.
  • molten steel having the composition is produced by a typically known method such as a converter or an electric furnace, then formed into a steel material such as a slab or billet by a typically known method such as a continuous casting method or an ingot making method. It is appreciated that the molten steel may be additionally subjected to treatment such as ladle metallurgy or vacuum degassing.
  • the steel material is preferably heated to a temperature of 1050 to 1250°C, then hot-rolled into desired size and shape.
  • the steel material is preferably directly hot-rolled into steel having the desired size and shape without being heated, or with being merely soaked.
  • hot-finish-rolling finishing temperature and a cooling rate after hot finish rolling are preferably appropriately adjusted, wherein the hot-finish-rolling finishing temperature is preferably 700°C or more, and cooling after hot finish rolling is finished is preferably performed by air cooling or accelerated cooling at a cooling rate of 100 °C/s or less. Reheating may be performed after cooling.
  • Steel having a composition shown in Table 2 was produced by a vacuum melting furnace or a converter, then slabs were loaded into a heating furnace and heated to 1150°C, and then hot-rolled into thick steel plates 25 mm in thickness, and then the steel plates obtained in such a way were examined in tensile and impact properties of mother material. Moreover, a heat cycle corresponding to submerge welding with input heat quantity of 150 kJ/cm was applied to the steel plates to simulate HAZ portions, and the simulated HAZ portions were provided for evaluation of an impact property (simulated-HAZ impact property).
  • test pieces 5 mm thick, 100 mm wide, and 200 mm long, and test pieces 5 mm thick, 50 mm wide, and 150 mm long were taken from the respective thick steel plates, then a surface of each of the test pieces was subjected to shot blasting, and then the test pieces were subjected to surface treatment at the following conditions A to C, so that exposure test pieces were prepared.
  • Condition A A double-layer film of a zinc primer film (about 15 ⁇ m) and a tar epoxy resin paint film (about 200 ⁇ m) was formed on a surface of a test piece.
  • Condition B A single-layer film of a tar epoxy resin paint film (about 200 ⁇ m) was formed on a surface of a test piece.
  • Condition C A surface of a test piece was subjected to shot blasting and remained bare (with no anti-corrosion film).
  • test pieces of the conditions A and B each test piece having a paint film, were provided with a scratch in 80 mm in length in a straight line, which reached a surface of base steel, by a box cutter through the paint film.
  • test pieces were attached to a back of an upper deck of a ballast tank of an actual ship so as to be provided for an exposure test.
  • a period of the exposure test was three years, and corrosion environment of the ballast tank was set as follows: about 20 days as a period in which seawater was filled in the ballast tank, and about 20 days as a period in which seawater was not filled therein were combined as one cycle, and the cycle was repeated.
  • corrosion resistance in the exposure test was evaluated in a way that area of a swollen paint film generated around the scratch was measured for evaluation.
  • Table 3 shows results of tensile and impact tests
  • Table 4 shows results of exposure for two years and exposure for three years. From the result of the exposure for three years in Table 4, it is known that steel of each of Nos. 1 to 20 as inventive examples, which satisfy the composition of the invention, is 50% or less in swollen-paint-film area and thickness-decrease-amount with respect to the base steel (No. 21) in any of the test pieces at the conditions A to C, and therefore has excellent corrosion resistance.
  • the ratio to the base steel is 73% at the condition of both the zinc primer paint film and the tar epoxy paint film in a result of the exposure for two years, the ratio is 42% in a result of the exposure for three years, showing the anti-corrosion effect of W and Cr being exhibited.
  • the anti-corrosion steel for ship of the invention has excellent corrosion resistance under corrosion environment due to seawater, therefore the steel can be used for a ballast tank of a ship, in addition, can be applied to other uses where the steel is used in similar corrosion environment.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Ocean & Marine Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Combustion & Propulsion (AREA)
  • Heat Treatment Of Steel (AREA)
  • Laminated Bodies (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)

Abstract

Anti-corrosion steel for ship is provided at low cost, which exhibits excellent corrosion resistance without depending on a surface condition of steel even under severe corrosion environment such as a ballast tank of a ship. Anti-corrosion steel for ship contains, in mass percent, C of 0.03 to 0. 25%, Si of 0. 05 to 0. 50%, Mn of 0.1 to 2.0%, P of 0.025% or less, S of 0.01% or less, Al of 0.005 to 0.10%, W of 0.01 to 1.0%, Cr of 0.01% or more and less than 0.20%, and furthermore contains as needed one or two selected from Sb of 0.001 to 0.3% and Sn of 0.001 to 0.3% and/or one or at least two selected from Ni of 0.005 to 0.25%, Mo of 0.01 to 0.5%, and Co of 0.01 to 1.0%, and contains the remainder including Fe and inevitable impurities.

Description

    Technical Field
  • The present invention relates to anti-corrosion steel used for ships such as a coal ship, an ore carrier, an ore coal carrier, a crude oil tanker, an LPG carrier, an LNG carrier, a chemical tanker, a container ship, a bulk carrier, a log carrier, a chip carrier, a refrigerated cargo ship, a pure car carrier, a heavy load carrier, a roll-on/roll-off ship, a limestone carrier, and a cement carrier, and particularly relates to anti-corrosion steel for ship used for a ballast tank and the like under a severe corrosion environment with seawater. The anti-corrosion steel for ship described in the invention includes a thick steel plate, sheet steel, shape sheet, and bar steel.
    • Background Art
  • Since a ballast tank of a ship serves to enable stable navigation of a ship by being poured with seawater while no cargo is loaded, the tank is placed in an extremely severe corrosion environment. Therefore, an anti-corrosion paint film using epoxy paint is formed, in addition, cathodic protection is applied for preventing corrosion of steel used for the ballast tank.
  • However, even if such anti-corrosion measures are taken, corrosion environment of the ballast tank is still in a severe condition. That is, when the ballast tank is poured with seawater, in the case that cathodic protection works, corrosion can be inhibited from being developed in a region that is perfectly dipped in the seawater. However, a region near a top of the ballast tank, a back of an upper deck is particularly not dipped in seawater, and situated while being sprayed with seawater. Therefore, cathodic protection does not work in such a region. Furthermore, since the region is increased in temperature of a steel plate by sunlight, the region is in a more severe corrosion environment, and consequently drastically corroded. Moreover, when the ballast tank is not poured with seawater, cathodic protection does not work at all, and consequently the tank is drastically corroded due to an effect of remaining adhesion salinity.
  • Life of an anti-corrosion paint film of a ballast tank is said to be typically about 10 years under such a drastic corrosion resistance, that is, half the life (20 years) of a ship. It is actual situation that corrosion resistance is kept by performing repair painting in the remaining ten years. However, since the ballast tank is in the severe corrosion environment as above, even if the repair painting is carried out, an effect of the painting is hard to be kept for a long time. Moreover, since the repair painting is performed as operation in a narrow space, operation environment is not preferable.. Thus, it is desirable to develop a steel material having an excellent corrosion resistance, which can lengthen a period before the repair painting to the utmost, and can reduce an operation load of the repair painting to the utmost.
  • Thus, several technologies have been proposed to improve corrosion resistance of steel itself used for a region placed in a severe corrosion environment such as the ballast tank. For example, patent document 1 discloses anti-corrosion low alloy steel including steel containing C of 0.20 mass% or less, the steel being added with Cu of 0.05 to 0.50 mass% and W of 0.01 to less than 0. 05 mass% as elements that improves corrosion resistance, and furthermore added with one or at least two of Ge, Sn, Pb, As, Sb, Bi, Te and Be in a range of 0.01 to 0.2 mass% as the elements. Patent document 2 discloses anti-corrosion low alloy steel including steel containing C of 0.20 mass% or less, the steel being added with Cu of 0.05 to 0.50 mass% and W of 0. 05 to 0. 5 mass% as elements that improves corrosion resistance, and furthermore added with one or at least two of Ge, Sn, Pb, As, Sb, Bi, Te and Be in a range of 0.01 to 0.2 mass% as the elements. Patent document 3 discloses anti-corrosion low alloy steel including steel containing C of 0.15 mass% or less, which is added with Cu of 0.05 to less than 0.15 mass% and W of 0.05 to 0.5 mass%.
  • Patent document 4 discloses a ballast tank in which anti-corrosion low alloy steel, which includes steel containing C of 0.15 mass% or less, the steel being added with P of 0.03 to 0.10 mass%, Cu of 0.1 to 1.0 mass%, and Ni of 0.1 to 1.0 mass% as elements that improve corrosion resistance, is coated with anti-corrosion paint such as tar epoxy paint, pure epoxy paint, epoxy paint without solvent, and urethane paint, and then covered with resin. This technology is intended to lengthen the life of anti-corrosion painting by improving corrosion resistance of steel itself, and thereby achieve a ship being free from maintenance over 20 to 30 years corresponding to the useful life of a ship.
  • Patent document 5 makes a proposal that steel containing C of 0.15 mass% or less is added with Cr of 0.2 to 5 mass% as an element that improves corrosion resistance in order to achieve a ship being free from maintenance. Furthermore, patent document 6 proposes an anti-corrosion method of a ballast tank characterized in that steel containing C of 0.15 mass% or less, which is added with Cr of 0.2 to 5 mass% as an element that improves corrosion resistance, is used as a componential material, and oxygen gas concentration within a ballast tank has a value in a ratio of 0.5 or less with respect to a value of oxygen gas concentration in air.
  • Patent document 7 makes a proposal that steel containing C of 0.1 mass% or less is added with Cr of 0.5 to 3.5 mass% to improve corrosion resistance, so that a ship being free from maintenance is achieved. Furthermore, patent document 8 discloses steel for ship in which steel containing C of 0.001 to 0.025 mass% is added with Ni of 0.1 to 4.0 mass% to improve paint-film damage resistance, so that maintenance cost for repair painting and the like is reduced.
  • Patent document 9 discloses steel for ship in which steel containing C of 0.01 to 0.25 mass% is added with Cu of 0.01 to 2.00 mass% and Mg of 0.0002 to 0.0150 mass% so as to have corrosion resistance in use environment such as a shell of a ship, a ballast tank, a cargo oil tank, and an iron-ore cargo hold. Furthermore, patent document 10 discloses steel in which steel containing C of 0.001 to 0.2 mass% is compositely added with Mo, W and Cu, and limited in the added amount of P and S as impurities, thereby general corrosion or local corrosion that may occur in a crude oil tank is inhibited.
  • However, each of the patent documents 1 to 3 does not make adequate investigation on corrosion resistance under presence of a paint film of Zinc-primer or epoxy paint being typically coated on steel configuring a ballast tank or the like. Therefore, further investigation is necessary for improving corrosion resistance under presence of the paint film.
  • The steel described in the patent document 4 is added with a comparatively large amount of P, 0.03 to 0.10 mass%, to improve corrosion resistance of base metal, which is problematic in a point of weldability and toughness of a weld. The steel described in each of the patent documents 5 and 6 is added with a comparatively large amount of Cr, 0.2 to 5 mass%. The steel described in the patent document 7 is added with a comparatively large amount of Cr, 0.5 to 3.5 mass%. Either of them is problematic in the point of weldability and toughness of a weld, in addition, problematic in that manufacturing cost is increased. The steel described in the patent document 8 is comparatively low in C content, and comparatively high in Ni content, which is problematic in that manufacturing cost is increased.
  • The steel described in the patent document 9 is problematic in that Mg is essentially added, which causes unstableness in yield of steel manufacture, leading to unstableness in mechanical properties of the steel. Furthermore, the steel described in the patent document 10 is anti-corrosion steel used in the crude oil tank, namely, used under an environment having H2S, and therefore the steel is unclear in corrosion resistance in the ballast tank having no H2S. Furthermore, since corrosion resistance has not been investigated in a condition that zinc-primer being typically used for steel for a ballast tank is coated, further investigation on corrosion resistance is necessary to be used for a ballast tank.
    • Patent document 1: JP-A-48-050921
    • Patent document 2: JP-A-48-050922
    • Patent document 3: JP-A-48-050924
    • Patent document 4: JP-A-07-034197
    • Patent document 5: JP-A-07-034196
    • Patent document 6: JP-A-07-034270
    • Patent document 7: JP-A-07-310141
    • Patent document 8: JP-A-2002-266052
    • Patent document 9: JP-A-2000-017381
    • Patent document 10: JP-A-2004-204344
    Disclosure of the Invention
  • Generally, a ship is built by welding steel materials such as a thick steel plate, sheet steel, shape steel, and bar steel, and surfaces of the steel materials are applied with anti-corrosion painting before use. The anti-corrosion painting is typically applied in a manner that zinc-primer is coated for primary rust prevention, and epoxy paint is coated as secondary painting (main painting) after subassembly or main assembly is performed. Therefore, the major part of steel surface of a ship has a double-layer structure thereon, which includes a zinc primer paint film and an epoxy paint film. However, since the zinc-primer is burned out by welding heat on a weld, zinc primer is repainted on the weld as touch up paint for rust prevention in a period after welding and before main painting. However, when the period before the main painting is short, repainting of zinc primer is not performed in some case. After a ship is built, the ship enters service, and in a ship that has been used for many years, there is a portion where the paint film is degraded and thus does not adequately act as a paint film, or there is a portion where the paint film is separated, so that a steel plate is bared.
  • As a result, three conditions exist on a surface of steel of a ship in service, including a portion of the double-layer structure in which a zinc primer paint film and an epoxy paint film are formed, a portion where only an epoxy paint film is formed, and a portion where the steel is bared. In any condition, steel having excellent corrosion resistance is required to improve corrosion resistance of the ship.
  • Thus, an object of the invention is to provide anti-corrosion steel for ship at low cost, which exhibits excellent corrosion resistance without depending on a surface condition of steel even under a severe corrosion environment such as a ballast tank of a ship, whereby a period before repair painting can be lengthened, consequently operation load of the repair painting can be reduced.
  • The inventors made earnest study for developing the steel that exhibits excellent corrosion resistance without depending on the surface condition of the steel even under the severe corrosion environment caused by seawater. As a result, the inventors found that W and Cr are contained as essential elements, in addition, elements that improve corrosion resistance such as Sb and Sn are contained in an appropriate range, thereby the steel that exhibits excellent corrosion resistance can be obtained in any of the conditions of the double-layer structure of a zinc primer paint film and an epoxy paint film, only an epoxy paint film, and bare steel, and consequently they completed the invention.
  • That is, the invention includes anti-corrosion steel for ship containing C of 0.03 to 0.25 mass%, Si of 0.05 to 0.50 mass%, Mn of 0.1 to 2.0 mass%, P of 0.025 mass% or less, S of 0.01 mass% or less, Al of 0.005 to 0.10 mass%, W of 0.01 to 1.0 mass%, Cr of 0.01 mass% or more and less than 0.20 mass%, N of 0.001 to 0.008 mass%, and the remainder including Fe and inevitable impurities.
  • The steel of the invention is characterized by containing a component in at least one group between the following groups A and B, in addition to the above composition.
  • Group A; one or two selected from Sb of 0. 001 to 0. 3 mass% and Sn of 0.001 to 0.3 mass%.
  • Group B; one or at least two selected from Ni of 0.005 to 0.25 mass%, Mo of 0.01 to 0.5 mass%, and Co of 0.01 to 1.0 mass.
  • Moreover, the steel of the invention is characterized by containing a component in at least one group among the following groups C to E, in addition to the above composition.
  • Group C; one or at least two selected from Nb of 0.001 to 0.1 mass%, Ti of 0. 001 to 0.1 mass%, Zr of 0. 001 to 0.1 mass%, and V of 0.002 to 0.2 mass%.
  • Group D; B of 0.0002 to 0.003 mass%.
  • Group E; one or at least two selected from Ca of 0.0002 to 0.01 mass%, REM of 0.0002 to 0.015 mass%, and Y of 0.0001 to 0.1 mass%.
  • Moreover, steel of the invention is characterized in that an epoxy paint film or a zinc primer paint film is formed on a surface of the steel, or both the zinc primer paint film and the epoxy paint film are formed thereon.
  • According to the invention, steel can be provided, the steel having excellent corrosion resistance even under a severe corrosion environment caused by seawater, which significantly contributes to lengthening of a period before repair painting, and reduction in operation load of repair painting.
    • Best Mode for Carrying Out the Invention
  • The inventors conducted the following experiment to develop steel having excellent corrosion resistance in any of the three portions that may exist on a surface of steel of a ship in service, that is, a portion of the double-layer structure of a zinc primer paint film and an epoxy paint film, a portion of only an epoxy paint film, and a bare steel portion.
  • Steel being added with various alloy elements were ingoted, then the ingots were hot-rolled into hot-rolled plates 5 mm in thickness, and then test pieces 5 mm thick, 100 mm wide, and 200 mm long, and test pieces 5 mm thick, 50 mm wide, and 150 mm long were taken from the hot-rolled plates. Then, a surface of each of the test pieces was subjected to shot blasting to remove scales or oil from the surface, and then the test pieces were subjected to the following three types of surface treatment, so that exposure test pieces were prepared.
  • Condition A: A double-layer film of a zinc primer film (about 15 µm) and a tar epoxy resin paint film (about 100 µm) is formed on a surface of a test piece.
  • Condition B: A single-layer film of a tar epoxy resin paint film (about 100 µm) is formed on a surface of a test piece.
  • Condition C: A surface of a test piece is subjected to shot blasting and remains bare (with no anti-corrosion film).
  • Then, the test pieces were subjected to a salt-spray alternate-drying-and-wetting corrosion test, which simulates a corrosion environment corresponding to a back of an upper deck of a ballast tank of an actual ship, based on a condition that an exposure test was performed by 132 cycles, each cycle including spraying of 5% NaCl solution at 35°C for 2 hr, leaving to stand at 60°C and RH25% for 4 hr, and leaving to stand at 50°C and RH95% for 2 hr, thereby the test pieces were evaluated in corrosion resistance. For the test pieces of the conditions A and B, each test piece having a paint film, corrosion resistance was evaluated in a way that a scratch in 80 mm in length, which reached a surface of base steel, was formed in a straight line by a box cutter through the paint film before the test, and area of a swollen paint film generated around the scratch was measured for evaluation after the test. For the test pieces having no paint film of the condition C, corrosion resistance was evaluated in a way that the test pieces were derusted after the test, and the average amount of decrease in thickness was calculated for evaluation from the amount of change in weight (amount of decrease) between the derusted test piece and a test piece before the test.
  • By summarizing results of the corrosion test, effects of respective alloy elements on corrosion resistance are collected in Table 1. Table 1
    Alloy element Condition of test piece used in corrosion resistance test
    Condition A
    (zinc primer paint film and tar epoxy resin paint film)    		 Condition B
    (tar epoxy resin paint film)    		 Condition C
    (bare steel)
    W 2 4 4
    Cr 5 0 0
    Sb 1 1 1
    Sn 0 1 1
    Ni, Mo, Co 0 to 1 0 (Ni, Co), 0 to 1 (Mo) 0 to 1
    W+Cr 6 4 4
    W+Cr+Sb+Sn 6 6 6
    • (Effect on corrosion resistance)
    • 0; no effect
    • 1 to 2; some effect
    • 4; large effect
    • 5 to 6; significantly large effect
    To briefly describe the results,
    1. 1) In the case of the condition A (double-layer paint film of the zinc primer paint film and the tar epoxy resin paint film), the most effective element for improving corrosion resistance is Cr, followed by W, and followed by Sb.
    2. 2) In the case of the condition B (only the tar epoxy resin paint film), the most effective element for improving corrosion resistance is W, followed by Sb, and followed by Sn.
    3. 3) In the case of the condition C (bare steel), the most effective element for improving corrosion resistance is W, followed by Sb, and followed by Sn.
    4. 4) When W and Cr are compositely contained, corrosion resistance at the condition A is improved compared with a case that each is singly contained, and furthermore, when Sb and Sn are contained in addition to them, a significant effect is exhibited in any of the conditions A, B and C.
    5. 5) Mo slightly improves corrosion resistance in any of the conditions A, B and C, and Ni and Co slightly improve corrosion resistance in the conditions A and C.
  • Based on the test results, the invention was designed to use a componential system in which W and Cr were compositely contained as essential elements for improving corrosion resistance. Furthermore, the invention was designed in a way that when more excellent corrosion resistance was required, a component design was used, in which one or two selected from Sb and Sn were contained in addition to W and Cr. Moreover, the invention was designed in a way that when further more excellent corrosion resistance was required, one or two or more selected from Ni, Mo and Co were additionally contained.
  • Next, a composition that the anti-corrosion steel for ship of the invention must have is specifically described.
    C: 0.03 to 0.25 mass%
  • C is an effective element for increasing strength of steel, and needs to be contained by 0.03 mass% or more to obtain a desired strength in the invention. On the other hand, when C is contained by more than 0.25 mass%, toughness of HAZ (weld heat-affected zone) is reduced. Accordingly, C is contained in a range of 0.03 to 0.25 mass%. From a viewpoint of naturally obtaining certain strength together with certain toughness by rolling, C is preferably contained in a range of 0.05 to 0.20 mass%.
    Si: 0.05 to 0.50 mass%
  • Si is an element to be added as a deoxidizer, or added for increasing strength of steel, and contained by 0.05 mass% or more in the invention. However, when Si is added by more than 0.50 mass%, toughness of steel is degraded, therefore an upper limit of Si is specified to be 0.50 mass%.
    Mn: 0.1 to 2.0 mass%
  • Mn is an element having an effect of preventing hot shortness, and increasing strength of steel, and added by 0.1 mass% or more. However, when Mn is added by more than 2.0 mass%, toughness of steel and weldability are reduced, therefore Mn is contained to be 2.0 mass% or less. Preferably, Mn is contained in a range of 0.5 to 1.6 mass%.
    P: 0.025 mass% or less
  • P is a harmful element that may degrade toughness of steel as mother material, and furthermore degrade weldability and toughness of a weld, and therefore P is preferably reduced to the utmost. In particular, when the content of P exceeds 0.025 mass%, toughness of mother material and toughness of a weld are more significantly reduced. Accordingly, P is contained to be 0.025 mass% or less. Preferably, P is contained to be 0.014 mass% or less.
    S: 0.01 mass% or less
  • Since S is a harmful element that may degrade toughness of steel and weldability, S is preferably reduced to the utmost, and contained to be 0.01 mass% or less in the invention.
    Al: 0.005 to 0.10 mass%
  • Al is an element to be added as a deoxidizer, and added by 0.005 mass% or more. However, when Al is contained by more than 0.10 mass%, Al3+ eluted due to corrosion of base steel reduces pH of a surface of the base steel, leading to degradation in corrosion resistance, therefore an upper limit of Al is specified to be 0.10 mass%.
    W: 0.01 to 1.0 mass%
  • W improves corrosion resistance under presence of both the zinc primer paint film and the epoxy paint film, and significantly improves corrosion resistance under presence of only the epoxy paint film. Moreover, W significantly improves corrosion resistance of steel even if the steel is bare. Therefore, W is one of the most important elements for improving corrosion resistance in the steel of the invention. The effect is exhibited in W content of 0.01 mass% or more. However, when W content is more than 1.0 mass%, the effect is saturated. Accordingly, the content of W is in a range of 0.01 to 1. 0 mass%.
  • The reason why W has the effect of improving corrosion resistance is because as a steel plate is corroded, WO4 2- is produced in produced rust, and presence of the WO4 2- prevents chloride ions from entering a steel plate surface, and furthermore sparingly-soluble FeWO4 is produced in a region having decreased pH such as an anode area of the steel plate surface, and presence of the FeWO4 also prevents chloride ions from entering the steel plate surface. The chloride ions are thus prevented from entering the steel plate surface, thereby corrosion of the steel plate is effectively inhibited. Moreover, inhibitor operation of WO4 2- also inhibits corrosion of steel.
    Cr: 0.01 mass% or more and less than 0.20 mass%
  • Since Cr exhibits excellent corrosion resistance under presence of both the zinc primer paint film and the epoxy paint film, Cr is one of the important elements in the steel of the invention. It is presumed that under presence of zinc primer, Zn in the zinc primer is eluted, so that Zn-based corrosion products such as ZnO and ZnCl2•4Zn(OH)2 are produced, and Cr acts on the Zn-based corrosion products so as to further improve corrosion prevention of base steel given by the Zn-based corrosion products. Such a corrosion resistance improvement effect of Cr under presence of the zinc primer is exhibited at the content of Cr of 0.01 mass% or more. However, when Cr is contained by 0.20 mass% or more, toughness of a weld is degraded. Accordingly, the content of Cr is in a range of 0.01 mass% or more and less than 0.20 mass%.
    N: 0.001 to 0.008 mass%
  • N is a harmful component for toughness, and desirably reduced to the utmost in order to achieve improvement in toughness. However, N is industrially hard to be decreased to less than 0.001 mass%. Conversely, when N is contained by 0.008 mass% or more, toughness is significantly degraded. Accordingly, the content of N is in a range of 0.001 to 0.008 mass% in the invention.
  • The steel of the invention may contain the following components in addition to the above components for the purpose of further improving corrosion resistance.
    One or two of 0.001 to 0.3 mass% Sb and 0.001 to 0.3 mass% Sn
  • Sb has an effect of improving corrosion resistance under presence of both the zinc primer paint film and the epoxy paint film, under presence of only the epoxy paint film, and in a condition of bare steel. Sn has an effect of improving corrosion resistance under presence of only the epoxy paint film, and in the condition of bare steel. The reason for the effects of Sb and Sn is considered to be that corrosion is inhibited in a region having decreased pH such as an anode area of the steel plate surface. While the effects are exhibited when either of Sn and Sb is contained by 0.001 mass% or more, in the case that the content is more than 0.3 mass%, toughness of each of mother material and HAZ is degraded, therefore each of Sn and Sb is preferably contained in a range of 0.001 to 0.3 mass%.
    One or at least two of 0.005 to 0.25 mass% Ni, 0.01 to 0.5 mass% Mo, and 0.01 to 1.0 mass% Co
  • Ni, Mo and Co slightly improve corrosion resistance under presence of both the zinc primer paint film and the epoxy paint film, and in the condition of bare steel. Furthermore, Mo slightly improves corrosion resistance even under presence of only the epoxy paint film. Therefore, when corrosion resistance is desired to be further improved, the elements may be supplementarily contained. The reason for the effects of Ni, Mo and Co is considered to be that they act to refine rust particles, in addition, Mo produces MoO4 2- in rust and thus prevents chloride ions from entering a steel plate surface. The effects are exhibited in the Ni content of 0.005 mass% or more, Mo content of 0.01 mass% or more, and Co content of 0.01 mass% or more respectively.
  • However, even if Ni of more than 0.25 mass%, Mo of more than 0.5 mass%, and Co of more than 1.0 mass% are added respectively, the respective effects are saturated, which is economically disadvantageous. Accordingly, Ni, Mo and Co are preferably contained in the above range respectively.
  • Furthermore, the steel of the invention may contain the following components in addition to the above components for increasing strength of steel and/or improving toughness.
    One or at least two of 0.001 to 0.1 mass% Nb, 0.001 to 0.1 mass% Ti, 0.001 to 0.1 mass% Zr, and 0.002 to 0.2 mass% V
  • Any of Nb, Ti, Zr and V is an element that improves strength of steel, and can be selectively contained depending on required strength. To obtain such an effect, preferably, each of Nb, Ti and Zr is contained by 0.001 mass% or more, and V is contained by.0.002 mass% or more. However, when Nb, Ti or Zr is added by more than 0.1 mass%, and when V is added by more than 0.2 mass%, toughness is reduced, therefore each of Nb, Ti, Zr and V is preferably added with each of the above values being specified as an upper limit value.
    B: 0.0002 to 0.003 mass%
  • B is an element that improves strength of steel, and can be contained as needed. To obtain the effect, B is preferably contained by 0.0002 mass% or more. However, when B is added by more than 0.003 mass%, toughness is degraded. Accordingly, B is preferably contained in a range of 0.0002 to 0.003 mass%.
    One or at least two of 0.0002 to 0.01 mass% Ca, 0.0002 to 0.015 mass% REM, and 0.0001 to 0.1 mass% Y
  • Any of Ca, REM and Y is an element having an effect of improving toughness of a weld heat-affected zone, and can be selectively contained as needed. While such an effect is obtained in the content of Ca of 0.0002 mass% or more, REM of 0. 0002 mass% or more, and Y of 0.0001 mass% or more respectively, when Ca of more than 0.01 mass%, REM of more than 0.015 mass%, and Y of more than 0.1 mass% are added respectively, toughness is rather reduced, therefore Ca, REM and Y are preferably contained with the above values being specified as upper limit values respectively.
  • The steel of the invention preferably contains Fe and inevitable impurities as components other than the above. However, it will be appreciated that the invention is not intended to reject to contain a component other than the above if an effect of the component is within a level at which it does not kill the effect of the invention.
  • Next, a preferable method of manufacturing the anti-corrosion steel according to the invention is described.
  • Preferably, molten steel having the composition is produced by a typically known method such as a converter or an electric furnace, then formed into a steel material such as a slab or billet by a typically known method such as a continuous casting method or an ingot making method. It is appreciated that the molten steel may be additionally subjected to treatment such as ladle metallurgy or vacuum degassing.
  • Next, the steel material is preferably heated to a temperature of 1050 to 1250°C, then hot-rolled into desired size and shape. Alternatively, when temperature of the steel material is high in a level at which the steel material can be hot-rolled, the steel material is preferably directly hot-rolled into steel having the desired size and shape without being heated, or with being merely soaked.
  • In hot rolling, to secure strength, hot-finish-rolling finishing temperature and a cooling rate after hot finish rolling are preferably appropriately adjusted, wherein the hot-finish-rolling finishing temperature is preferably 700°C or more, and cooling after hot finish rolling is finished is preferably performed by air cooling or accelerated cooling at a cooling rate of 100 °C/s or less. Reheating may be performed after cooling.
    • Example
  • Steel having a composition shown in Table 2 was produced by a vacuum melting furnace or a converter, then slabs were loaded into a heating furnace and heated to 1150°C, and then hot-rolled into thick steel plates 25 mm in thickness, and then the steel plates obtained in such a way were examined in tensile and impact properties of mother material. Moreover, a heat cycle corresponding to submerge welding with input heat quantity of 150 kJ/cm was applied to the steel plates to simulate HAZ portions, and the simulated HAZ portions were provided for evaluation of an impact property (simulated-HAZ impact property).
  • Next, test pieces 5 mm thick, 100 mm wide, and 200 mm long, and test pieces 5 mm thick, 50 mm wide, and 150 mm long were taken from the respective thick steel plates, then a surface of each of the test pieces was subjected to shot blasting, and then the test pieces were subjected to surface treatment at the following conditions A to C, so that exposure test pieces were prepared.
  • Condition A: A double-layer film of a zinc primer film (about 15 µm) and a tar epoxy resin paint film (about 200 µm) was formed on a surface of a test piece. Condition B: A single-layer film of a tar epoxy resin paint film (about 200 µm) was formed on a surface of a test piece. Condition C: A surface of a test piece was subjected to shot blasting and remained bare (with no anti-corrosion film).
  • The test pieces of the conditions A and B, each test piece having a paint film, were provided with a scratch in 80 mm in length in a straight line, which reached a surface of base steel, by a box cutter through the paint film.
  • Then, the test pieces were attached to a back of an upper deck of a ballast tank of an actual ship so as to be provided for an exposure test. A period of the exposure test was three years, and corrosion environment of the ballast tank was set as follows: about 20 days as a period in which seawater was filled in the ballast tank, and about 20 days as a period in which seawater was not filled therein were combined as one cycle, and the cycle was repeated. For the test pieces of the conditions A and B, each test piece having the paint film, corrosion resistance in the exposure test was evaluated in a way that area of a swollen paint film generated around the scratch was measured for evaluation. For the test pieces of the condition C having no paint film, corrosion resistance was evaluated in a way that the test pieces were derusted after the test, and the average amount of decrease in thickness was calculated from the amount of change in weight (amount of decrease) between the derusted test piece and a test piece before the test, and then assuming that No. 21 steel without containing any particular element that improves corrosion resistance was base steel (100), a ratio of a value of each test piece to a value of the base steel was calculated for evaluation.
  • Table 3 shows results of tensile and impact tests, and Table 4 shows results of exposure for two years and exposure for three years. From the result of the exposure for three years in Table 4, it is known that steel of each of Nos. 1 to 20 as inventive examples, which satisfy the composition of the invention, is 50% or less in swollen-paint-film area and thickness-decrease-amount with respect to the base steel (No. 21) in any of the test pieces at the conditions A to C, and therefore has excellent corrosion resistance. In the steel of No. 20, while the ratio to the base steel is 73% at the condition of both the zinc primer paint film and the tar epoxy paint film in a result of the exposure for two years, the ratio is 42% in a result of the exposure for three years, showing the anti-corrosion effect of W and Cr being exhibited.
  • On the contrary, in steel of each of Nos. 22 to 24 that do not satisfy the composition of the invention, even if corrosion resistance is improved compared with the base steel (No. 21), the ratio to the base steel is more than 50% in some condition. In No. 26, since Al content exceeds the upper limit value, corrosion resistance is degraded in all the conditions. In steel of each of Nos. 25 and 27, while a ratio of corrosion resistance to the base steel is 50% or less, an impact property of a weld is significantly degraded.
    • Industrial Applicability
  • The anti-corrosion steel for ship of the invention has excellent corrosion resistance under corrosion environment due to seawater, therefore the steel can be used for a ballast tank of a ship, in addition, can be applied to other uses where the steel is used in similar corrosion environment. Table 2
    Steel No. Component (mass%)
    C Si Mn P S Al W Cr N Sb, Sn Ni, Mo, Co Nb, Ti, Zr, V B Ca, REM, Y Remarks
    1 0.15 0.32 0.95 0.009 0.002 0.030 0.05 0.01 0.0030 - - - - - Inventive example
    2 0.13 0.32 1.32 0.013 0.003 0.029 0.20 0.15 0.0028 - - - - - Inventive example
    3 0.14 0.31 1.41 0.011 0.002 0.029 0.36 0.08 0.0027 - - - - - Inventive example
    4 0.12 0.32 1.35 0.012 0.003 0.030 0.06 0.07 0.0028 Sb:0.11 - - - - Inventive example
    5 0.08 0.31 1.45 0.010 0.002 0.025 0.07 0.10 0.0025 Sb:0.09 Sn:0.04 - - - - Inventive example
    6 0.10 0.28 1.33 0.009 0.002 0.035 0.04 0.02 0.0030 Sb:0.11 Sn:0.03 - Ti:0.011 - - Inventive example
    7 0.05 0.35 1.57 0.007 0.002 0.033 0.01 0.03 0.0015 Sn:0.23 - - - - Inventive example
    8 0.05 0.32 1.51 0.006 0.001 0.032 0.05 0.03 0.0041 Sb:0.01 Sn:0.15 - Ti:0.015 - - Inventive example
    9 0.03 0.15 1.58 0.006 0.002 0.028 0.10 0.06 0.0016 Sb:0.24 - - 0.0007 - Inventive example
    10 0.05 0.28 1.57 0.012 0.002 0.025 0.05 0.02 0.0038 Sb:0.10 Sn:0.01 - - - - Inventive example
    11 0.10 0.30 1.35 0.011 0.002 0.028 0.15 0.16 0.0035 - Ni:0.21 - - - Inventive example
    12 0.12 0.25 1.05 0.011 0.003 0.031 0.04 0.07 0.0029 - Ni:0.01 Mo:0.38 Co:0.15 - - - Inventive example
    13 0.08 0.29 1.15 0.008 0.003 0.029 0.45 0.18 0.0045 Sn:0.10 - Ti:0.012 - - Inventive example
    14 0.07 0.35 0.95 0.009 0.002 0.031 0.07 0.07 0.0035 - Mo:0.15 Nb:0.012 Zr:0.007 V:0.04 - - Inventive example
    15 0.11 0.32 1.35 0.011 0.003 0.028 0.06 0.02 0.0028 Sb:0.09 Sn:0.04 Ni:0.01 - 0.0007 - Inventive example
    16 0.14 0.35 1.25 0.008 0.003 0.025 0.81 0.06 0.0015 Sb:0.15 Co:0.02 Ti:0.003 0.0005 - Inventive example
    17 0.09 0.15 1.47 0.009 0.002 0.035 0.02 0.19 0.0031 - Ni:0.04 Co:0.05 - - Ca:0.0018 Inventive example
    18 0.08 0.25 1.45 0.011 0.003 0.025 0.15 0.10 0.0038 Sb:0.05 Mo:0.05 Ti:0.018 - REM:0.0030 Inventive example
    19 0.11 0.29 1.42 0.009 0.003 0.029 0.05 0.07 0.0021 - - Zr:0.005 - REM:0.0010 Y:0.01 Inventive example
    20 0.12 0.32 1.38 0.013 0.002 0.031 0.12 0.03 0.0030 Sb:0.10 - - - - Inventive example
    21 0.14 0.31 1.45 0.011 0.004 0.029 - - 0.0035 - - - - - Comparative example
    22 0.13 0.30 1.43 0.012 0.004 0.031 0.08 - 0.0030 - - - - - Comparative example
    23 0.11 0.32 1.36 0.013 0.003 0.028 - 0.07 0.0031 - - - - - Comparative example
    24 0.10 0.33 1.29 0.011 0.002 0.029 0.03 - 0.0031 Sb:0.08 Sn:0.05 - - - - Comparative example
    25 0.13 0.31 1.36 0.012 0.003 0.031 0.12 0.75 0.0031 - - - - - Comparative example
    26 0.12 0.32 1.25 0.012 0.003 0.383 0.21 - 0.0035 - - - - - Comparative example
    27 0.13 0.30 1.24 0.041 0.003 0.028 0.15 0.18 0.0026 - - - - - Comparative example
    Table 3
    Steel No. Mechanical properties of mother material Impact property of weld vE (0°C) (J) Remarks
    Tensile properties Impact property vE(-20°C)(J)
    YS(MPa) TS(MPa) EI(%)
    1 387 512 30 228 132 Inventive example
    2 395 538 32 235 152 Inventive example
    3 402 556 36 245 151 Inventive example
    4 396 556 36 223 135 Inventive example
    5 385 541 35 217 142 Inventive example
    6 376 518 32 269 145 Inventive example
    7 391 511 31 285 136 Inventive example
    8 378 519 32 298 133 Inventive example
    9 359 514 30 289 151 Inventive example
    10 361 551 34 272 147 Inventive example
    11 400 536 37 207 126 Inventive example
    12 365 527 36 215 126 Inventive example
    13 373 542 37 252 189 Inventive example
    14 389 539 31 265 195 Inventive example
    15 379 546 32 234 166 Inventive example
    16 381 554 37 254 164 Inventive example
    17 384 538 34 242 198 Inventive example
    18 376 547 32 269 211 Inventive example
    19 391 541 35 228 178 Inventive example
    20 379 525 36 236 125 Inventive example
    21 358 525 34 225 105 Comparative example
    22 388 526 36 225 119 Comparative example
    23 378 539 33 219 131 Comparative example
    24 372 541 32 221 129 Comparative example
    25 385 555 31 158 41 Comparative example
    26 375 535 36 118 96 Comparative example
    27 385 537 36 84 21 Comparative example
    Table 4
    Steel No. Results of exposure test (two years) Results of exposure test (three years) Remarks
    Zinc primer paint film and tar epoxy paint film Tar epoxy paint film Bare steel Zinc primer paint film and tar epoxy paint film Tar epoxy paint film Bare steel
    Area of swollen paint film (ratio to base steel: %) Area of swollen paint film (ratio to base steel: %) Amount of decrease in thickness (ratio to base steel: %) Area of swollen paint film (ratio to base steel:%) Area of swollen paint film (ratio to base steel: %) Amount of decrease in thickness (ratio to base steel: %)
    1 46 47 43 44 39 40 Inventive example
    2 36 43 42 26 32 33 Inventive example
    3 40 38 38 26 25 25 Inventive example
    4 39 36 36 30 35 36 Inventive example
    5 30 33 34 29 33 34 Inventive example
    6 42 43 41 40 36 37 Inventive example
    7 45 49 48 43 42 44 Inventive example
    8 40 43 40 39 35 36 Inventive example
    9 34 41 38 29 33 34 Inventive example
    10 40 42 39 39 35 37 Inventive example
    11 33 41 40 24 34 33 Inventive example
    12 31 39 39 30 38 37 Inventive example
    13 35 34 33 20 21 20 Inventive example
    14 40 37 37 31 36 37 Inventive example
    15 40 43 36 38 34 34 Inventive example
    16 30 21 19 21 17 15 Inventive example
    17 30 43 44 27 44 44 Inventive example
    18 33 37 37 26 31 31 Inventive example
    19 48 46 45 34 39 40 Inventive example
    20 73 47 48 42 33 34 Inventive example
    21 100 100 100 100 100 100 Comparative example
    22 75 49 49 73 43 38 Comparative example
    23 62 95 98 60 92 93 Comparative example
    24 57 43 41 56 40 36 Comparative example
    25 35 49 48 17 41 36 Comparative example
    26 135 149 162 132 148 149 Comparative example
    27 36 44 42 25 39 35 Comparative example

Claims (9)

  1. Anti-corrosion steel for ship, comprising:
    C of 0.03 to 0.25 mass%,
    Si of 0.05 to 0.50 mass%,
    Mn of 0.1 to 2.0 mass%,
    P of 0.025 mass% or less,
    S of 0.01 mass% or less,
    Al of 0.005 to 0.10 mass%,
    W of 0.01 to 1.0 mass%,
    Cr of 0.01 mass% or more and less than 0.20 mass%,
    N of 0.001 to 0.008 mass%, and
    the remainder including Fe and inevitable impurities.
  2. The anti-corrosion steel for ship according to claim 1, characterized by containing:
    one or two selected from Sb of 0.001 to 0.3 mass% and Sn of 0.001 to 0.3 mass% in addition to the composition.
  3. The anti-corrosion steel for ship according to claim 1 or 2, characterized by further containing:
    one or at least two selected from Ni of 0.005 to 0. 25 mass%, Mo of 0.01 to 0.5 mass%, and Co of 0.01 to 1.0 mass in addition to the composition.
  4. The anti-corrosion steel for ship according to any one of claims 1 to 3, characterized by further containing:
    one or at least two selected from Nb of 0.001 to 0.1 mass%, Ti of 0.001 to 0.1 mass%, Zr of 0.001 to 0.1 mass%, and V of 0.002 to 0.2 mass% in addition to the composition.
  5. The anti-corrosion steel for ship according to any one of claims 1 to 4, characterized by further containing:
    B of 0.0002 to 0.003 mass% in addition to the composition.
  6. The anti-corrosion steel for ship according to any one of claims 1 to 5, characterized by further containing:
    one or at least two selected from Ca of 0.0002 to 0.01 mass%, REM of 0.0002 to 0.015 mass%, and Y of 0.0001 to 0. 1 mass% in addition to the composition.
  7. The anti-corrosion steel for ship according to any one of claims 1 to 6, characterized in that:
    an epoxy paint film is formed on a surface of the steel.
  8. The anti-corrosion steel for ship according to any one of claims 1 to 6, characterized in that:
    a zinc primer paint film is formed on a surface of the steel.
  9. The anti-corrosion steel for ship according to any one of claims 1 to 6, characterized in that:
    a zinc primer paint film and an epoxy paint film are formed on a surface of the steel.
EP07707040.7A 2006-02-27 2007-01-12 Corrosion-resistant steel material for ship and vessel Expired - Fee Related EP1990437B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2006050451 2006-02-27
PCT/JP2007/050736 WO2007097142A1 (en) 2006-02-27 2007-01-12 Corrosion-resistant steel material for ship and vessel

Publications (3)

Publication Number Publication Date
EP1990437A1 true EP1990437A1 (en) 2008-11-12
EP1990437A4 EP1990437A4 (en) 2015-03-11
EP1990437B1 EP1990437B1 (en) 2016-08-31

Family

ID=38437186

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07707040.7A Expired - Fee Related EP1990437B1 (en) 2006-02-27 2007-01-12 Corrosion-resistant steel material for ship and vessel

Country Status (5)

Country Link
EP (1) EP1990437B1 (en)
KR (2) KR101115275B1 (en)
CN (1) CN101389782B (en)
DK (1) DK1990437T3 (en)
WO (1) WO2007097142A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2808411A4 (en) * 2012-01-25 2015-10-21 Jfe Steel Corp Corrosion-resistant steel for hold of coal carrying vessel or coal/ore carrying vessel

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5396758B2 (en) 2007-07-27 2014-01-22 Ｊｆｅスチール株式会社 Hot-rolled section steel for ship ballast tank and manufacturing method thereof
JP5320919B2 (en) * 2007-09-25 2013-10-23 Ｊｆｅスチール株式会社 Hot rolled shape steel for crude oil tank and method for producing the same
WO2009041703A1 (en) * 2007-09-25 2009-04-02 Jfe Steel Corporation Hot-rolled shape steel for crude oil tanks and process for manufacturing the same
JP4502075B1 (en) * 2008-12-24 2010-07-14 Ｊｆｅスチール株式会社 Corrosion resistant steel for crude oil tankers
KR20110018445A (en) * 2009-03-30 2011-02-23 신닛뽄세이테쯔 카부시키카이샤 Corrosion-resistant steel for use in chimney or flue of natural gas combustion or liquefied petroleum gas combustion plant
CN103667892B (en) * 2013-11-29 2016-04-13 国家电网公司 The ground net alloy material that a kind of acid resistance soil corrosion is wear-resisting
CN104372246A (en) * 2014-11-11 2015-02-25 江苏省沙钢钢铁研究院有限公司 400 MPa-level tungstenic corrosion-resistant twisted steel and preparation method thereof
WO2016098234A1 (en) * 2014-12-18 2016-06-23 新日鐵住金株式会社 Steel material, ship ballast tank and hold formed using said steel material, and ship equipped with said ballast tank or hold
CN104831172A (en) * 2015-04-23 2015-08-12 苏州劲元油压机械有限公司 Manufacturing method of fixing plate for hydraulic pressure station
CN105568174A (en) * 2016-02-03 2016-05-11 福建海峡西岸知识产权研究院有限公司 Semi-submerged ship structural material and preparing method thereof
CN107540119A (en) * 2016-06-29 2018-01-05 北京联合创业环保工程股份有限公司 A kind of processing method of the high organic wastewater of high salt
CN105970086B (en) * 2016-06-29 2018-04-20 巢湖鹏远金属焊管有限公司 High-strength corrosion-resisting straight welded pipe steel
CN106854737A (en) * 2016-12-15 2017-06-16 苏州赛斯德工程设备有限公司 A kind of outdoor cabinet anticorrosive steel
CN107034419A (en) * 2017-06-21 2017-08-11 合肥博创机械制造有限公司 A kind of corrosion-resistant metal materials and its production technology
CN113025924B (en) * 2021-02-07 2022-05-20 首钢集团有限公司 Steel for ultrahigh-strength dual-phase corrosion-resistant stirring tank and production process thereof

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54131522A (en) * 1978-04-03 1979-10-12 Nippon Steel Corp Steel highly resistant against hydrogen induced blister and cracking
DE3070501D1 (en) * 1979-06-29 1985-05-23 Nippon Steel Corp High tensile steel and process for producing the same
JP2822853B2 (en) * 1993-07-15 1998-11-11 住友金属工業株式会社 Durable ballast tank
JP4081991B2 (en) * 2000-04-25 2008-04-30 Ｊｆｅスチール株式会社 Corrosion resistant steel for freight oil tank and method for producing the same
JP4483107B2 (en) * 2001-03-09 2010-06-16 Ｊｆｅスチール株式会社 Marine steel with excellent coating life
JP5044874B2 (en) * 2001-05-11 2012-10-10 Ｊｆｅスチール株式会社 Painted steel with excellent corrosion resistance
JP3753088B2 (en) * 2001-07-04 2006-03-08 住友金属工業株式会社 Steel material for cargo oil tanks
JP4267367B2 (en) * 2002-06-19 2009-05-27 新日本製鐵株式会社 Crude oil tank steel and its manufacturing method, crude oil tank and its anticorrosion method
JP4449691B2 (en) * 2004-04-14 2010-04-14 住友金属工業株式会社 Steel material for cargo oil tanks

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2007097142A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2808411A4 (en) * 2012-01-25 2015-10-21 Jfe Steel Corp Corrosion-resistant steel for hold of coal carrying vessel or coal/ore carrying vessel

Also Published As

Publication number Publication date
KR20080090541A (en) 2008-10-08
CN101389782A (en) 2009-03-18
EP1990437A4 (en) 2015-03-11
KR101115275B1 (en) 2012-03-14
KR20110084462A (en) 2011-07-22
CN101389782B (en) 2011-05-25
WO2007097142A1 (en) 2007-08-30
EP1990437B1 (en) 2016-08-31
DK1990437T3 (en) 2016-09-19

Similar Documents

Publication Publication Date Title
EP1990437B1 (en) Corrosion-resistant steel material for ship and vessel
TWI391499B (en) Hot-rolled shape steel for ships and process for manufacturing the same
JP4525687B2 (en) Corrosion resistant steel for ships
JP5119595B2 (en) Corrosion resistant steel for shipbuilding
JP5861335B2 (en) Welded joint with excellent corrosion resistance
EP2395120A1 (en) Corrosion resistant steel for crude oil tank, manufacturing method therefor, and crude oil tank
JP5617191B2 (en) Marine steel with excellent film swell resistance
JP5453835B2 (en) Corrosion resistant steel for ships
JP5796409B2 (en) Corrosion resistant steel for ship ballast tank
JP5481980B2 (en) Marine steel with excellent film swell resistance
JP5076961B2 (en) High strength marine corrosion resistant steel with excellent high heat input weld toughness and method for producing the same
JP2000017381A (en) Corrosion resistant steel for shipbuilding
JP5958102B2 (en) Corrosion-resistant steel for ship ballast tank with excellent corrosion resistance and method for producing the same
JP5958103B2 (en) Steel material for marine ballast tanks with excellent paint swell resistance
CN109790607B (en) Steel material for ship ballast tank and ship
JP5526667B2 (en) Hot rolled section steel for ship ballast tank with excellent corrosion resistance and method for producing the same
JP2010229526A (en) Highly-corrosion-resistant painted steel material
JP6493019B2 (en) Corrosion-resistant steel for ballast tanks
JP6772942B2 (en) Corrosion resistant steel for ballast tanks
JP5157519B2 (en) Corrosion-resistant steel for marine vessels with excellent high heat input weld toughness and method for producing the same
JP6048104B2 (en) Corrosion resistant steel for holding coal ships and coal / ore combined ships
JP2011162849A (en) Zinc primer-coated corrosion resistant steel material
JP2011094184A (en) Highly corrosion resistant painted steel
JP6736255B2 (en) Corrosion resistant steel for ballast tanks
JP5157518B2 (en) Corrosion-resistant steel for marine vessels with excellent high heat input weld toughness and method for producing the same

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20080716

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE DK FR

RBV Designated contracting states (corrected)

Designated state(s): DE DK FR

DAX Request for extension of the european patent (deleted)
RBV Designated contracting states (corrected)

Designated state(s): DE DK FR

A4 Supplementary search report drawn up and despatched

Effective date: 20150211

RIC1 Information provided on ipc code assigned before grant

Ipc: B63B 3/00 20060101ALI20150205BHEP

Ipc: C21D 9/46 20060101ALI20150205BHEP

Ipc: C22C 38/12 20060101ALI20150205BHEP

Ipc: C22C 38/00 20060101AFI20150205BHEP

Ipc: C21D 7/06 20060101ALI20150205BHEP

Ipc: C22C 38/02 20060101ALI20150205BHEP

Ipc: C22C 38/60 20060101ALI20150205BHEP

Ipc: C22C 38/38 20060101ALI20150205BHEP

Ipc: C22C 38/16 20060101ALI20150205BHEP

Ipc: C21D 8/02 20060101ALI20150205BHEP

Ipc: C21D 9/50 20060101ALI20150205BHEP

Ipc: C22C 38/22 20060101ALI20150205BHEP

Ipc: C22C 38/14 20060101ALI20150205BHEP

Ipc: C22C 38/06 20060101ALI20150205BHEP

Ipc: C22C 38/04 20060101ALI20150205BHEP

Ipc: C21D 8/06 20060101ALI20150205BHEP

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

RIC1 Information provided on ipc code assigned before grant

Ipc: C21D 8/06 20060101ALI20150916BHEP

Ipc: C22C 38/06 20060101ALI20150916BHEP

Ipc: C22C 38/02 20060101ALI20150916BHEP

Ipc: C21D 8/02 20060101ALI20150916BHEP

Ipc: C22C 38/16 20060101ALI20150916BHEP

Ipc: B63B 3/00 20060101ALI20150916BHEP

Ipc: C22C 38/60 20060101ALI20150916BHEP

Ipc: C22C 38/22 20060101ALI20150916BHEP

Ipc: C22C 38/12 20060101ALI20150916BHEP

Ipc: C21D 9/50 20060101ALI20150916BHEP

Ipc: C21D 9/46 20060101ALI20150916BHEP

Ipc: C22C 38/38 20060101ALI20150916BHEP

Ipc: C22C 38/00 20060101AFI20150916BHEP

Ipc: C22C 38/04 20060101ALI20150916BHEP

Ipc: C22C 38/14 20060101ALI20150916BHEP

Ipc: C21D 7/06 20060101ALI20150916BHEP

INTG Intention to grant announced

Effective date: 20151007

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20160330

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE DK FR

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

Effective date: 20160915

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602007047703

Country of ref document: DE

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 11

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602007047703

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20170601

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20211217

Year of fee payment: 16

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DK

Payment date: 20220110

Year of fee payment: 16

Ref country code: DE

Payment date: 20211130

Year of fee payment: 16

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602007047703

Country of ref document: DE

REG Reference to a national code

Ref country code: DK

Ref legal event code: EBP

Effective date: 20230131

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230801

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230131

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230131