Stainless steel clad steel plate including cladding material for stainless steel clad steel plate and method of manufacturing the same

Abstract

A cladding material for stainless steel clad steel plate, includes, by mass %, 0.03% or less carbon, 1.5% or less silicon, 2.0% or less manganese, 0.04% or less phosphorus, 0.03% or less sulfur, 22.0% to 25.0% nickel, 21.0% to 25.0% chromium, 2.0% to 5.0% molybdenum, 0.15% to 0.25% nitrogen, and the balance being iron and incidental impurities, wherein critical pitting temperature (CPT) after normalization as determined in accordance with ASTM G48-03 Method E is 45 C. or higher, and corrosion loss at a welded zone as determined by a corrosion test in accordance with NORSOK Standard M-601 is 1.0 g/m.sup.2 or less.

Claims

1. A stainless steel clad steel plate comprising the cladding material for stainless steel clad steel plate, consisting of, by mass %, 0.03% or less carbon, 1.5% or less silicon, 2.0% or less manganese, 0.04% or less phosphorus, 0.03% or less sulfur, 22.0% to 25.0% nickel, 21.0% to 25.0% chromium, 2.0% to 5.0% molybdenum, 0.15% to 0.25% nitrogen, optionally 0.0010% to 0.0055% boron, and the balance being iron and incidental impurities, wherein the critical pitting temperature (CPT) after normalization as determined in accordance with ASTM G48-03 Method E is 45 C. or higher, and the corrosion loss at a welded zone as determined by a corrosion test in accordance with NORSOK Standard M-601 is 1.0 g/m.sup.2 or less, and a carbon steel or a low-alloy steel as a base material, and having a total thickness of 30 to 100 mm.

2. The stainless steel clad steel plate according to claim 1, wherein an area percentage of (sigma) phase precipitated in a surface of the cladding material is 2.0% or less.

3. The stainless steel clad steel plate according to claim 1, wherein the cladding material precipitates extracted from the cladding material by constant-current electrolysis with 10% by volume acetylacetone-1% by mass tetramethylammonium chloride-methanol contain a chromium content of 0.5% by mass or less and molybdenum content of 0.3% by mass or less.

4. The stainless steel clad steel plate according to claim 3, wherein an area percentage of a phase precipitated in a surface of the cladding material is 2.0% or less.

5. A method of manufacturing the stainless steel clad steel plate according to claim 1, comprising hot rolling with a sacrificial material at a reduction ratio of 5 or more and then normalizing by heating to 850 C. to 950 C. and air cooling.

Description

DETAILED DESCRIPTION

(1) To provide good sea water corrosion resistance, the composition, manufacturing conditions, and other properties of the stainless steel clad steel plate need to be specified.

(2) 1. The grounds for the limitations on the composition of the stainless steel used as the cladding material will be described first. In the following description, percentage % denotes by mass % unless otherwise stated.

(3) Carbon: 0.03% or Less

(4) A lower carbon content is preferred in terms of corrosion resistance, particularly in a weld heat-affected zone. The carbon content therefore needs to be limited to 0.03% or less. Preferably, the carbon content is 0.020% or less.

(5) Silicon: 1.5% or Less

(6) Although a silicon content of 0.02% or more is necessary for deoxidization, a silicon content of more than 1.5% would significantly decrease the hot workability. Thus, the silicon content should be 1.5% or less. Preferably, the silicon content is 0.60% or less.

(7) Manganese: 2.0% or Less

(8) Although a manganese content of 0.02% or more is necessary for deoxidization, a manganese content of more than 2.0% would decrease the corrosion resistance. Thus, the manganese content should be 2.0% or less. Preferably, the manganese content is 0.60% or less.

(9) Phosphorus: 0.04% or Less, Sulfur: 0.03% or Less

(10) Although a lower phosphorus content and a lower sulfur content are preferred in terms of hot workability, a phosphorus content of more than 0.04% and a sulfur content of more than 0.03% would decrease the hot workability. Thus, the phosphorus content should be 0.04% or less, and the sulfur content should be 0.03% or less. Preferably, the phosphorus content is 0.03% or less, and the sulfur content is 0.01% or less.

(11) Nickel: 22.0% to 25.0%

(12) A nickel content of 22.0% or more is necessary in terms of austenite phase stability, mainly depending on the balance with the chromium and molybdenum contents. The nickel content, however, should be 25.0% or less, taking into account economy and the increase in hot deformation resistance due to increased nickel content. To achieve a balance of austenite phase stability and economy, a nickel content of 22.0% to 24.5% is preferred. More preferably, the nickel content is 22.5% to 24.0%.

(13) Chromium: 21.0% to 25.0%

(14) A chromium content of 21.0% or more is necessary because chromium is effective in improving pitting corrosion resistance and crevice corrosion resistance. A chromium content of more than 25.0%, however, significantly promotes precipitation of a phase during the manufacture of the cladding material, and at clad rolling and cooling, therefore decreasing the corrosion resistance and the hot workability. Thus, the chromium content should be 21.0% to 25.0%. To improve the pitting corrosion resistance and the crevice corrosion resistance while inhibiting precipitation of a phase, a chromium content of 21.0% to 24.0% is preferred. More preferably, the chromium content is 22.0% to 23.5%.

(15) Molybdenum: 2.0% to 5.0%

(16) A molybdenum content of 2.0% or more is necessary because molybdenum is effective in improving the pitting corrosion resistance and the crevice corrosion resistance. A molybdenum content of more than 5.0%, however, would significantly promote precipitation of a phase during the manufacture of the cladding material, and at clad rolling and cooling, therefore decreasing the corrosion resistance and the hot workability. Thus, the molybdenum content should be 2.0% to 5.0%. To improve the pitting corrosion resistance and the crevice corrosion resistance while inhibiting precipitation of a phase, a molybdenum content of 2.0% to 4.5% is preferred. More preferably, the molybdenum content is 2.5% to 3.5%.

(17) Nitrogen: 0.15% to 0.25%

(18) Nitrogen is effective in improving the corrosion resistance. To achieve this effect, the nitrogen content should be 0.15% or more. A nitrogen content of more than 0.25%, however, is not practical because of its relationship with the contents of other elements. Thus, the nitrogen content should be 0.15% to 0.25%. Preferably, the nitrogen content is 0.18% to 0.22%.

(19) Whereas the cladding material for stainless steel clad steel plate has the foregoing basic composition, the balance being iron and incidental impurities, it may further contain boron within the following range.

(20) Boron: 0.0010% to 0.0055%

(21) Boron is effective in improving corrosion resistance and hot workability. To achieve this effect, the boron content should be 0.0010% or more. A boron content of more than 0.0055%, however, would decrease the corrosion resistance and the hot workability. Thus, if boron is present, the boron content is preferably 0.0010% to 0.0055%. More preferably, the boron content is 0.0015% to 0.0035%.

(22) The balance is iron and incidental impurities. The cladding material may contain trace amounts of other elements that do not interfere with the advantageous effects described above.

(23) The base material for stainless steel clad steel plate may be a carbon steel or a low-alloy steel.

(24) The stainless steel clad steel plate has a thickness (total thickness) of 30 to 100 mm. In particular, a stainless steel clad steel plate having such a thickness is required in marine structures, vessels such as FPSO, and sea water desalination equipments.

(25) The stainless steel clad steel plate is manufactured by cladding one or both surfaces of the base material with the stainless steel having the composition described above as the cladding material.

(26) 2. The sea water corrosion resistance of the stainless steel used as the cladding material will then be described.

(27) (a) The critical pitting temperature (CPT) after normalization as determined in accordance with ASTM G48-03 Method E is 45 C. or higher.

(28) The base material for stainless steel clad steel plate requires properties suitable for use as a structural material in marine structures, vessels such as FPSO, and sea water desalination equipments. Accordingly, hot rolling is often followed by normalization involving heating to 850 C. to 950 C. and air cooling. This treatment applies the same thermal history to the stainless steel used as the cladding material. To provide sufficient sea water corrosion resistance after such a thermal history, the critical pitting temperature (CPT) should be 45 C. or higher. Thus, the critical pitting temperature (CPT) as determined in accordance with ASTM G48-03 Method E should be 45 C. or higher. The test method will be described in the Examples section.

(29) (b) The corrosion loss at a welded zone as determined by a corrosion test in accordance with NORSOK Standard M-601 is 1.0 g/m.sup.2 or less.

(30) A clad steel plate is often used as a welded structural member, rather than used alone. Accordingly, the stainless steel used as the cladding material is also welded. To provide sufficient sea water corrosion resistance, the corrosion loss at a welded zone as determined by a corrosion test in accordance with NORSOK Standard M-601 needs to be 1.0 g/m.sup.2 or less. Examples of welding method include submerged arc welding, MIG welding, and MAG welding. The heat input at welding is preferably 50 kJ/cm or less.

(31) A CPT of 45 C. or higher and a corrosion loss of 1.0 g/m.sup.2 or less are achieved by controlling the composition of the stainless steel used as the cladding material and employing the manufacturing method described later. The test method will be described in the Examples section.

(32) The corrosion resistance of the stainless steel used as the cladding material is further specified by the following properties.

(33) (c) Precipitates extracted by constant-current electrolysis with 10% by volume acetylacetone-1% by mass tetramethylammonium chloride-methanol preferably contain a chromium content of 0.5% by mass or less and a molybdenum content of 0.3% by mass or less.

(34) The use of constant-current electrolysis allows the amount of precipitates in steel to be quantitatively evaluated. The extracted precipitates can be analyzed by X-ray diffraction (XRD) to precisely identify the type of precipitates.

(35) The sea water corrosion resistance of the a phase is evaluated from the contents of chromium and molybdenum in the a phase. The chromium content of the precipitates is 0.5% by mass or less because a chromium content of more than 0.5% by mass would degrade the pitting corrosion resistance. A chromium content of 0.3% by mass or less is more preferred in terms of pitting corrosion resistance.

(36) The molybdenum content of the precipitates is 0.3% by mass or less because a molybdenum content of more than 0.3% by mass would degrade the pitting corrosion resistance. A molybdenum content of 0.2% by mass or less is more preferred in terms of pitting corrosion resistance.

(37) (d) The area percentage of the a phase precipitated in the surface of the cladding material is 2.0% or less.

(38) A large amount of a phase precipitated is undesirable because it would decrease the chromium and molybdenum contents of the austenite phase around the a phase and would therefore degrade the pitting corrosion resistance. Specifically, an area percentage of more than 2.0% is undesirable because it would degrade the pitting corrosion resistance. The area percentage is determined by examining the microstructure at about 400 magnification and performing image analysis on the micrograph. The microstructure of the a phase is analyzed in advance by a technique such as energy-dispersive X-ray spectroscopy to determine that the microstructure has high chromium and molybdenum contents.

(39) 3. Next, a method of manufacturing a stainless steel clad steel plate is specified.

(40) (a) The stainless steel clad steel plate is manufactured by rolling using a sacrificial material at a reduction ratio of 5 or more.

(41) The sacrificial material is used to prevent warpage after rolling.

(42) If hot rolling is used to manufacture a stainless steel clad steel plate, which is a composite material of an austenite stainless steel (cladding material) and a carbon steel (base material), the warpage generates during the hot rolling or cooling because the two types of steels have different deformation resistances and thermal expansion coefficients. To prevent such a warpage, a method using a sacrificial material is employed, in which a carbon steel plate is welded to a surface of the austenite stainless steel along the periphery thereof before hot rolling.

(43) The hot rolling is performed at a reduction ratio of 5 or more because high-temperature rolling at a reduction ratio of 5 or more produces a coupling force between the steels and thus provides good adhesion.

(44) (b) The hot rolling is followed by normalization involving heating to 850 C. to 950 C. and air cooling.

(45) As described above, because the base material for stainless steel clad steel plate requires the properties suitable for use as a structural material in marine structures, vessels such as FPSOs, and sea water desalination equipments, hot rolling is often followed by normalization involving heating to 850 C. to 950 C. and air cooling. The heating is performed to 850 C. to 950 C. because heating to 850 C. or higher is effective in improving the microstructure. Heating above 950 C. would not be effective in improving the microstructure because it would coarsen crystal grains. The cooling is performed by air cooling because rapid cooling would cause strain due to the difference in thermal expansion coefficient between the cladding material and the base material. Specifically, the cooling rate is 0.8 C./s or less.

EXAMPLES

(46) Examples will now be described.

(47) Austenite stainless steels having the compositions shown in Table 1 and SS400 steels (hereinafter abbreviated as ordinary steel) were used. SS400 steels having a thickness of 150 mm, serving as base materials, austenite stainless steels having a thickness of 13 mm, serving as cladding materials, and ordinary steels having a thickness of 26 mm, serving as sacrificial materials on the surface of the cladding materials, were combined to slabs having a thickness of (150+13+26) mm.

(48) These slabs were heated to 1,230 C., hot finish-rolled at 970 C., retained at 910 C. for 10 minutes, and cooled in air to manufacture stainless steel clad steel plates having a thickness of (29.5+2.5) mm.

(49) The pitting corrosion resistance of the cladding material of the thus-manufactured stainless steel clad steel plates was evaluated in accordance with ASTM G48-03 Method E, described later. The pitting corrosion resistance at a welded zone was then evaluated by a corrosion test using a welding test specimen described below. The welding test specimen was fabricated by forming X-grooves, welding the base material using a low-alloy welding wire, and TIG welding the cladding material in argon gas using a 625 alloy welding material having a diameter of 1.2 mm in accordance with JIS Z3334. The cladding material was TIG welded in four passes at a welding current of 200 A, a welding voltage of 25 V, and a welding speed of 30 cm/min. After excess welded part was removed from the surface layer of the cladding material, a test specimen having a thickness of 2.0 mm, a width of 20 mm, and a length of 50 mm was cut from the stainless steel clad steel plate. The test specimen included the welded zone and the heat-affected zone which were present with a ratio of 1:1. The corrosion loss was determined in accordance with ASTM G48-03 Method A, described later.

(50) To evaluate the amount of phase precipitates, the chromium and molybdenum contents of the precipitates extracted by electrolytic extraction were determined. The electrolyte used was 10% by volume acetylacetone-1% by mass tetramethylammonium chloride-methanol. A residue extracted by constant-current electrolysis was filtered off through a 0.2 m mesh organic filter and was decomposed by heating with a mixed acid (0.8% by mass tartaric acid and 10% by mass sulfuric acid). The chromium and molybdenum contents were determined by ICP emission spectroscopy.

(51) Critical Pitting Temperature (CPT): ASTM G48-03 Method E

(52) A dipping test was performed at various temperatures in increments of 5 C. in a 6% by mass FeCl.sub.3 and 1% by mass HCl solution for 24 hours. This dipping test was performed three times. A stainless steel clad steel plate in which a pitting corrosion depth of 0.025 mm or more occurred was evaluated as unacceptable. A stainless steel clad steel plate in which no pitting corrosion occurred was evaluated as acceptable. The maximum temperature reached by a stainless steel clad steel plate evaluated as unacceptable was determined as CPT ( C.). A CPT of 45 C. or higher was evaluated as good. A CPT of 50 C. or higher is more preferred.

(53) Ferric Chloride Test: ASTM G48-03 Method A

(54) A dipping test was performed in a 6% by mass FeCl.sub.3 solution at 40 C. for 24 hours. The corrosion loss was determined from the weight loss after the dipping test. The target corrosion loss is 1.0 g/m.sup.2 or less, preferably 0.8 g/m.sup.2 or less.

(55) TABLE-US-00001 TABLE 1 mass % Corrosion Cr content Mo content loss at a of of CPT welded zone precipitates precipitates No. C Si Mn P S Ni Cr Mo B N ( C.) (g/m.sup.2) (mass %) (mass %) Remarks 1 0.019 0.31 0.51 0.024 0.009 23.1 23.4 3.5 0.0002 0.202 45 0.69 0.10 0.07 Example 2 0.018 0.29 0.58 0.028 0.006 23.4 23.4 3.4 0.0001 0.199 45 0.64 0.10 0.05 Example 3 0.017 0.28 0.61 0.023 0.007 22.9 23.2 3.1 0.0003 0.210 50 0.54 0.09 0.03 Example 4 0.015 0.27 0.50 0.023 0.008 23.0 23.0 3.1 0.0022 0.190 50 0.51 0.08 0.03 Example 5 0.020 0.35 1.30 0.030 0.005 23.1 23.1 3.5 0.0016 0.200 50 0.61 0.09 0.03 Example 6 0.010 0.45 1.18 0.009 0.001 23.2 23.2 4.0 0.0030 0.190 45 0.76 0.14 0.16 Example 7 0.009 0.37 1.22 0.018 0.003 22.9 22.9 4.5 0.0025 0.182 45 0.79 0.15 0.15 Example 8 0.017 0.23 0.77 0.012 0.010 23.1 23.1 2.7 0.0020 0.211 45 0.74 0.13 0.11 Example 9 0.022 0.50 0.66 0.015 0.009 23.0 23.0 2.2 0.0021 0.195 45 0.86 0.17 0.21 Example 10 0.016 0.28 1.01 0.021 0.009 23.4 22.4 3.2 0.0018 0.199 50 0.73 0.09 0.04 Example 11 0.021 0.31 0.78 0.031 0.011 23.4 23.8 3.0 0.0031 0.210 45 0.83 0.21 0.11 Example 12 0.019 0.38 0.95 0.015 0.008 23.1 24.2 3.1 0.0045 0.194 45 0.84 0.22 0.15 Example 13 0.030 0.44 0.60 0.040 0.030 22.9 24.8 3.2 0.0012 0.190 45 0.81 0.21 0.13 Example 14 0.014 0.30 1.12 0.031 0.009 22.8 22.1 3.0 0.0023 0.201 45 0.91 0.30 0.12 Example 15 0.022 0.51 1.03 0.034 0.007 23.9 23.2 3.0 0.0041 0.187 50 0.69 0.09 0.04 Example 16 0.011 0.36 0.98 0.024 0.018 24.2 23.1 2.9 0.0023 0.191 50 0.71 0.10 0.05 Example 17 0.019 0.33 0.78 0.022 0.017 24.5 23.5 3.1 0.0021 0.210 45 0.87 0.33 0.21 Example 18 0.023 0.41 0.96 0.021 0.007 22.5 23.7 3.1 0.0019 0.194 45 0.82 0.41 0.20 Example 19 0.014 0.23 0.84 0.030 0.009 22.3 23.2 3.0 0.0029 0.196 45 0.81 0.43 0.22 Example 20 0.016 0.46 1.14 0.024 0.005 23.0 22.9 5.5 0.0019 0.211 35 5.12 0.65 0.45 Comparative example 21 0.018 0.37 1.21 0.020 0.003 23.1 22.8 6.2 0.0022 0.194 30 6.24 0.78 0.51 Comparative example 22 0.020 0.29 0.87 0.027 0.007 23.3 23.7 1.5 0.0023 0.196 35 5.66 0.71 0.44 Comparative example 23 0.023 0.35 0.57 0.031 0.009 22.8 21.0 3.1 0.0021 0.195 30 6.12 0.88 0.48 Comparative example 24 0.019 0.37 0.67 0.028 0.010 23.1 21.5 3.2 0.0019 0.191 30 6.01 0.81 0.51 Comparative example 25 0.015 0.24 0.89 0.024 0.007 23.0 26.5 3.0 0.0029 0.213 30 5.84 0.78 0.44 Comparative example 26 0.018 0.29 1.13 0.029 0.008 22.7 23.4 2.8 0.0019 0.204 25 3.12 0.57 0.42 Comparative example 27 0.024 0.31 1.34 0.032 0.009 23.1 23.7 2.9 0.0022 0.193 35 3.30 0.55 0.38 Comparative example 28 0.020 0.30 0.87 0.037 0.009 23.2 23.1 3.0 0.0030 0.186 35 3.11 0.56 0.35 Comparative example Note: The underlined values are beyond the scope of the present invention.

(56) As shown in Table 1, our examples have the target properties, i.e., a CPT of 45 C. or higher and a corrosion loss at a welded zone of 1.0 g/m.sup.2 or less as determined in accordance with ASTM G48-03 Method A at 40 C. for 24 hours, demonstrating that they have good sea water corrosion resistance.