CA2049050A1 - Manufacturing method of high corrosion-resistant low-alloy steel for line pipes - Google Patents
Manufacturing method of high corrosion-resistant low-alloy steel for line pipesInfo
- Publication number
- CA2049050A1 CA2049050A1 CA002049050A CA2049050A CA2049050A1 CA 2049050 A1 CA2049050 A1 CA 2049050A1 CA 002049050 A CA002049050 A CA 002049050A CA 2049050 A CA2049050 A CA 2049050A CA 2049050 A1 CA2049050 A1 CA 2049050A1
- Authority
- CA
- Canada
- Prior art keywords
- steel
- less
- temperature
- low
- alloy steel
- 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.)
- Abandoned
Links
- 230000007797 corrosion Effects 0.000 title claims abstract description 23
- 238000005260 corrosion Methods 0.000 title claims abstract description 23
- 229910000851 Alloy steel Inorganic materials 0.000 title claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 59
- 239000010959 steel Substances 0.000 claims abstract description 59
- 238000005096 rolling process Methods 0.000 claims abstract description 29
- 239000011651 chromium Substances 0.000 claims abstract description 21
- 239000010955 niobium Substances 0.000 claims abstract description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000010949 copper Substances 0.000 claims abstract description 10
- 239000011572 manganese Substances 0.000 claims abstract description 10
- 239000010936 titanium Substances 0.000 claims abstract description 10
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 8
- 229910052758 niobium Inorganic materials 0.000 claims abstract description 7
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 7
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 6
- 230000001186 cumulative effect Effects 0.000 claims abstract description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 5
- 239000011593 sulfur Substances 0.000 claims abstract description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000012535 impurity Substances 0.000 claims abstract description 4
- 239000011574 phosphorus Substances 0.000 claims abstract description 4
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 3
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 3
- 229910052742 iron Inorganic materials 0.000 claims abstract description 3
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims abstract description 3
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000010703 silicon Substances 0.000 claims abstract description 3
- 238000001816 cooling Methods 0.000 claims description 11
- 239000011575 calcium Substances 0.000 claims description 10
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 229910052720 vanadium Inorganic materials 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 15
- 230000002542 deteriorative effect Effects 0.000 abstract description 4
- 238000003303 reheating Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000005336 cracking Methods 0.000 description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052748 manganese Inorganic materials 0.000 description 3
- 238000004881 precipitation hardening Methods 0.000 description 3
- 238000003466 welding Methods 0.000 description 3
- MOMWFXLCFJOAFX-UHFFFAOYSA-N OOOOOOOO Chemical compound OOOOOOOO MOMWFXLCFJOAFX-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 230000003749 cleanliness Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- IHPYMWDTONKSCO-UHFFFAOYSA-N 2,2'-piperazine-1,4-diylbisethanesulfonic acid Chemical compound OS(=O)(=O)CCN1CCN(CCS(O)(=O)=O)CC1 IHPYMWDTONKSCO-UHFFFAOYSA-N 0.000 description 1
- KUGRPPRAQNPSQD-UHFFFAOYSA-N OOOOO Chemical compound OOOOO KUGRPPRAQNPSQD-UHFFFAOYSA-N 0.000 description 1
- OZBZONOEYUBXTD-UHFFFAOYSA-N OOOOOOOOO Chemical compound OOOOOOOOO OZBZONOEYUBXTD-UHFFFAOYSA-N 0.000 description 1
- 239000007990 PIPES buffer Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000009749 continuous casting Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
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
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/28—Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
-
- 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
-
- 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
- C22C38/001—Ferrous alloys, e.g. steel alloys containing N
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Heat Treatment Of Steel (AREA)
- Heat Treatment Of Articles (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
A manufacturing method of high corrosion-resistant low-alloy steel for line pipes improved in CO2 corrosion resistance without deteriorating low-temperature toughness of base material and weld heat-affected zone and field weldability. The invention steel comprises, by weight %, 0.02 to 0.09 carbon, 0.5 or less silicon, 0.7 to 1.5 manganese, 0.03 or less phosphorus, 0.005 or less sulfur, 0.02 to 0.06 niobium, 0.5 to not more than 1.2 chromium, 0.005 to 0.03 titanium, 0.05 or less aluminum, 0.002 to 0.005 nitrogen, and the balance of iron and unavoidable impurities, and satisfies the following equation: 0.35 ? C + (Mn + Cr + V)/5 + (Ni + Cu)/15 ? 0.48.
The steel is heated at a temperature in a range of 1100°C
to 1250°C, rolled with the cumulative rolling reduction at 950°C or less being 40% or more, a finish rolling temperature of 700°C to 850°C, and then, air-cooled or acceleratedly cooled.
A manufacturing method of high corrosion-resistant low-alloy steel for line pipes improved in CO2 corrosion resistance without deteriorating low-temperature toughness of base material and weld heat-affected zone and field weldability. The invention steel comprises, by weight %, 0.02 to 0.09 carbon, 0.5 or less silicon, 0.7 to 1.5 manganese, 0.03 or less phosphorus, 0.005 or less sulfur, 0.02 to 0.06 niobium, 0.5 to not more than 1.2 chromium, 0.005 to 0.03 titanium, 0.05 or less aluminum, 0.002 to 0.005 nitrogen, and the balance of iron and unavoidable impurities, and satisfies the following equation: 0.35 ? C + (Mn + Cr + V)/5 + (Ni + Cu)/15 ? 0.48.
The steel is heated at a temperature in a range of 1100°C
to 1250°C, rolled with the cumulative rolling reduction at 950°C or less being 40% or more, a finish rolling temperature of 700°C to 850°C, and then, air-cooled or acceleratedly cooled.
Description
-1- 2~0~a 17/3 SPECIFICATION
MANUFACTURING METHOD OF HIGH CORROSION-RESISTANT
LOW-ALLOY STEEL FOR LINE PIPES
The present invention relates to a manufacturing method of high strength steel plates for line pipes ~tensile strength: 50 kg f/mm2 or more by TS, thickness of 40 mm or less) which are excellent in the corrosion resistance to CO2.
BACKGROUND ART
Large-diameter line pipes for transportation of oil or natural gas in cold regions or offshores require not only high strength but also low-temperature toughness and field weldability. Further, the effect of inhibitors is lowered due to injection of CO2 in secondary and tertiary crude oil recovery and increase in the depth of oil wells, and for such reasons, corrosion of line pipes by CO2 gas has become a serious problem lately. Therefore, the corrosion resistance to CO2 has come to be demanded as well.
Although recently it is the knowledge that addition of Cr is effective against CO2 corrosion (Journal of Petroleum Technology Association, Vol. 50, No. 2, Figs.
9 and 10), there have not been developed large-diameter line pipes having the corrosion resistance to C2 which are perfectly suitable for low-temperature ~ ~ d~ O
1 environment yet.
In other words, although a number of steels to which Cr is added in large quantities to improve corrosion resistance have been developed (for example, JP-B-59-19179 and JP-B-59-45750), none of them is excellent in both low-temperature toughness and field weldability as line pipes for low-temperature environment.
Since addition of Cr in large quantities degrades the weldability of the steels, preheating and stress relief heat treatment at high temperature are essential in the view point of preventing weld cracking at the time of weld-ing in fields, thereby the work efficiency is deteriorated to a great extent. Further, addition of Cr in large quantities into the steel deteriorates the toughness of the base material of the steel and weld heat-affected zones (HAZ). Therefore, development of steel for line pipes excellent in the corrosion resistance to CO2 and having favorable low-temperature toughness and favorable field weldability is strongly demanded.
DISCLOSURE OF THE INVENTION
Accordingly, the principal object of the present invention is to a provide novel steel for line pipes which is greatly improved in the corrosion resistance to CO2 without deteriorating low-temperature toughness of the base material and the HAZ.
The object is achieved firstly by preparing a steel of which composition is, by weight ~, 0.02 to 0.09 2 ~ o 1 carbon, 0.5 or less silicon, 0.7 to 1.5 manganese, 0.03 or less phosphorus, 0.005 or less sulfur, 0.02 to 0.06 niobium, 0.5 to not more than 1.2 chromium, 0.005 to 0.03 titanium, 0.05 or less aluminum, 0.002 to 0.005 nitrogen, and the balance of iron and unavoidable impurities, and which satisfies the equation: 0.35 S C + (Mn + Cr + V)/5 +
(Ni + Cu)/15 S 0.48, and secondly by processing the steel in accordance with the following steps: heating a block of the steel to a temperature in a range of 1100C to 1250C, rolling the block at 950C or less and at 700C to 850C of a finish rolling temperature with a cumulatine rolling reduction of 40% or more, and air-cooling or accelerated cooling the rolled product. Thus, the desired steel product can be obtained.
Further, if necessary, one element or more selected from the group consisting of 0.01 to 0.08 V, 0.05 to 0.5 Ni, 0.05 to 0.5 Cu and 0.001 to 0.005 Ca can be added to the steel of the above mentioned composition.
The present invention will be hereinafter described in detail.
In order to improve the corrosion resistance to C2 and obtain excellent low-temperature toughness of the base material and the HAZ and excellent field weldability, it is necessary to select a particular chemical composition of the steel. For this reason, the Cr content is set at 0.5 to 1.2% in respect of the corrosion resistance. The Cr content is required to be 0.5% at least to obtain adequate corrosion resistance. However, too much Cr 2 ~
1 largely deteriorates the low-temperature toughness and the field weldability. Therefore, the upper limit is set at 1.2%.
When a considerable amount of Cr is added to the steel to improve the corrosion resistance, 0.02 to 0.09%
of C (carbon) and 0.7 to 1.5% of Mn are necessary for ensuring excellent low-temperature toughness and excellent weldability. The lower limits of C and Mn are minimum amounts for obtaining the required strength of the base material and welded joints and achieving the effects of precipitation hardening and grain refining of Nb and V when these elements are added to the steel. The upper limits are critical values for obtaining excellent low-temperature toughness and excellent field weldability (most preferable C and Mn contents are 0~03 to 0.06% and 0.8 to 1.2%, respectively).
Yet, it is insufficient to restrict the content of each element only. The following equation has to be satisfied: 0.35% S C + (Mn + Cr + V)/5 + (Ni + Cu)/15 0.48. This is because low-temperature toughness and weldability are determined by a total amount of chemical components including Cr. The lower limit of 0.35~ is a minimum amount for obtaining the required strength of the base material and welded ioints, and 0.48% is the upper limit for obtaining excellent low-temperature toughness and excellent weldability.
The steel of the invention contains 0.02 to 0.06% Nb and 0.005 to 0.03% Ti as essential elements.
2 ~ ~ ~J ~
1 Nb contributes to refining of grain size and precipitation hardening in controlled rolling, thus toughening the steel. By adding Ti to the steel, fine TiN are formed, and coarsening of y grains is suppressed during slab-reheating and welding, effectively improving the basematerial toughness and the HAZ toughness.
When a large amount of Cr is added to the steel, separations are inhibited on impact fracture surfaces of the control-rolled steel in Charpy test or the like, thereby deteriorating the low-temperature toughness.
Particularly in the steel of the present invention containing small amounts of C and Mn, therefore, addition of Nb and Ti was found to be essential in relation to obtaining the excellent low-temperature toughness.
The lower limits of Nb and Ti contents are minimum amounts for these elements to achieve their effects, and the upper limits are critical values of addition amounts not to deteriorate the HAZ toughness and the field weldability.
Reasons for restricting the amounts of the other elements will be described.
When Si is added excessively to the steel, the weldability and the HAZ toughness are lowered, and consequently, the upper limit is set at 0.5~. Deoxidation of the steel can be sufficiently performed by Ti alone, and it is not always necessary to add Si to the steel.
The reason why contents of impurities of P ~phosphorus) and S (sulfur) are set at 0.03% or less and 1 0.005% or less, respectively, in the steel of the invention is that the low-temperature toughness of the base material and the welded joints can be further improved as a result.
Reduction in the P content prevents inter-granular cracking, and reduction in the S content prevents the roughness from being deteriorated by MnS. Preferable P and S contents are 0.01% or less and 0.003% or less, respectively.
Although al is an element which the steel usually contains for deoxidation, it is not always necessary to add it to the steel because deoxidation can be effected by Ti or Si. When the Al content exceeds 0.05%. Non-metallic inclusions are increased to degrade cleanliness of the steel. Therefore, the upper limit is set at 0.05%.
Nitrogen (N) serves to form TiN and improve the toughness of the base material and the HAZ through the effect of suppressing the coarsening of ~ grains. The minimum content for this purpose is 0.002%. However, too much N causes deterioration of the HAZ toughness by solute nitrogen and slab surface defects, so that it is necessary to lower the upper limit to 0.005% or less.
Reasons for adding V, Ni, Cu and Ca to the steel will now be described.
A main object of further adding these elements to the base compositions is to improve the properties such as strength and toughness without spoiling excellent characteristics of the steel of the present invention.
Consequently, addition amounts of them have to be naturally restricted.
_ 7 _ 2~ 0 1 Vanadium (V) takes substantially the same effects as Nb such as improvement of the low-temperature toughness and increase in strength due to refinement of the micro-structure, increase in the strength owing to precipitation hardening, and so forth. However, excessive addition of V induces deteriorations of the weldability and the HAZ
toughness, and therefore, the upper limit is set at 0.08%.
Ni improves both the strength and the toughness without giving unfavorable influences to the wledability and the HAZ toughness, and it is also effective in prevention of hot cracks at the time of addition of Cu to the steel. However, the content exceeding 0.5% is not preferable economically, and accordingly, the upper limit is set at 0.5%.
Although Cu is effective in corrosion resistance and resistance against hydrogen induced cracking, the content exceeding 0.5% causes copper-cracks during hot rolling, resulting in difficulty in the manufacture of the steel. Therefore, the upper limit is set at 0.5%.
Calcium (Ca) controls the shape of a sulfide (MnS) and improves the low-temperature toughness (increase in Charpy absorption energy and the like), and it is also effective remarkably in improvement of the resistance against hydrogen-induced cracking. However, the Ca content not more than 0.001% has no effect in practice, and addition of Ca exceeding 0.005% induces generation of large amounts of CaO and CaS which become to coarse inclusions, not only degrading cleanliness of the steel - 8 - ~ 9 1 but also giving unfavorable influences to the toughness and the field weldability.
For this reason, the amount of Ca is limited to 0.001 to 0.005%. In order to improve the resistance against hydrogen-induced cracking, it is especially effective to reduce the sulfur (S) and oxygen (O~ contents to 0.001% or less and 0.002~ or less, respectively, and to satisfy the following equation: ESSP ' (Ca)[l - 124(0)]/1.25(S) 2 1.5. In this case, ESSP stands for Effective Sulfide Shape Controlling Parameter, and indicates a relation in the composition which prevents the sulfide from being extended in the rolling process.
More specifically, when the ESSP is set to 1.5 or more, the amount of MnS is reduced, and the amount of CaS, CaOS
which are not easily extended at the time of rolling is formed instead.
As for the above described steel containing Cr, an appropriate manufacturing method must be adopted to improve the low-temperature toughness of the base material, and it i8 necessary to restrict conditions of reheating, rolling and cooling of the steel (slabs).
First, the reheating temperature is restricted to a range of 1100 to 1250C. The reheating temperature has to be not less than 1100C to dissolve Nb precipitates into matrix and to obtain a finish rolling temperature as high as required. However, when the reheating temperature exceeds 1250C, austenitic ~Y) grains become to be considerably coarse, and can not be refined - 9 - 2~4 1 sufficiently even by rolling, so that excellent low-temperature toughness can not be obtained. Thus, the reheating temperature is set at not more than 1250C
(preferably, 1150 to 1200C).
Moreover, the cumulative rolling reduction at 950C or less must be set at not less than 40%, and the finish rolling temperature has to be set at 700 to 850C.
This is because ~ grains which have been refined by recrystallized region rolling are extended by low temperature rolling in the unrecrystallized region, so that resultant ferrite grain size is reduced to a minimum, thus improving the low temperature toughness. When the cumulative rolling reduction is under 40%, extending of the austenitic structure is insufficient, and therefore, fine ferritic grains can not be obtained.
Besides, when the finish rolling temperature is 850C or more, fine ferrite grains can not be obtained even if the cumulative rolling reduction is not less than 40~. However, when the finish rolling temperature is too low, it results in excessive two phase (~ + ~) of austenitic and ferritic phases region rolling, thus deteriorating the low temperature toughness. Therefore, the lower limit of the finish rolling temperature is set at 700C.
Air cooling or accelerated cooling is desirable for cooling after rolling. As a condition of the accelerated cooling, it is preferable to cool the steel to a desired temperature of not more than 600C at a -- 1 o -- 2 ~
1 cooling speed of 10 to 40C/sec immediately after cooling, and to air-cool it thereafter. The advantage of the present invention will not be lost even if the manufactured steel is reheated at a temperature not more than ACl point for the purpose of tempering, dehydrogenation and so forth.
EXAMPLES
Steel plates (15 to 32 mm thick) having various steel compositions were manufactured through converter process, continuous casting process and plate rolling process, and examined in respect of strength, toughness, low-temperature toughness and corroslon resistance.
Test items and results are shown in Table 1.
All of the steel plates (steels of the present invention) manufactured according to the invention method have favorable properties. On the other hand, comparative steels which were not manufactured according to the present invention are inferior in strength, low-temperature toùghness or corrosion resistance.
As for comparative steels 11 to 19, a steel 11 whose Cr content is low is inferior in the corrosion resistance. A steel 12 whose Cr content is excessive is inferior in the weldability, with Pc (= C + (Mn + Cr +
V)/5 + (Ni + Cu)/15) being high, and the HAZ toughness is also inferior. A steel 13 whose carbon content is high is inferior in the low-temperature toughness of both the base material and the HAZ. A steel 14 whose Mn content is - 11 2~
1 high is inferior in the HAZ toughness. A steel 15 contains no Nb so that the strength of the base material is low, and that the toughness is inferior as well. A steel 16 containing no Ti is inferior in the toughness of the base material and the HAZ. As for a steel 17, the reheating tempexature is low, and consequently, the base material strength is insufficient. A steel 18 is inferior in the base material toughness because the cumulative rolling reduction at 950C or less is insufficient. Further, a steel 19 whose finish rolling temperature is too low is inferior in the base material toughness.
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1 As will be apparent from the above, according to the present invention, there can be produced line pipes having improved corrosion resistance to C02 and high strength which are excellent in field weldability. As a result, efficiency of welding work in fields and safety of pipe lines are remarkably improved.
INDUSTRIAL APPLICABILITY
The steel manufactured according to the invention method is superior in low temperature toughness and corrosion resistance to C02, and it is also excellent in field weldability. It is suitable for large-diameter line pipes for transportation of oil or natural gas in cold regions and offshores.
MANUFACTURING METHOD OF HIGH CORROSION-RESISTANT
LOW-ALLOY STEEL FOR LINE PIPES
The present invention relates to a manufacturing method of high strength steel plates for line pipes ~tensile strength: 50 kg f/mm2 or more by TS, thickness of 40 mm or less) which are excellent in the corrosion resistance to CO2.
BACKGROUND ART
Large-diameter line pipes for transportation of oil or natural gas in cold regions or offshores require not only high strength but also low-temperature toughness and field weldability. Further, the effect of inhibitors is lowered due to injection of CO2 in secondary and tertiary crude oil recovery and increase in the depth of oil wells, and for such reasons, corrosion of line pipes by CO2 gas has become a serious problem lately. Therefore, the corrosion resistance to CO2 has come to be demanded as well.
Although recently it is the knowledge that addition of Cr is effective against CO2 corrosion (Journal of Petroleum Technology Association, Vol. 50, No. 2, Figs.
9 and 10), there have not been developed large-diameter line pipes having the corrosion resistance to C2 which are perfectly suitable for low-temperature ~ ~ d~ O
1 environment yet.
In other words, although a number of steels to which Cr is added in large quantities to improve corrosion resistance have been developed (for example, JP-B-59-19179 and JP-B-59-45750), none of them is excellent in both low-temperature toughness and field weldability as line pipes for low-temperature environment.
Since addition of Cr in large quantities degrades the weldability of the steels, preheating and stress relief heat treatment at high temperature are essential in the view point of preventing weld cracking at the time of weld-ing in fields, thereby the work efficiency is deteriorated to a great extent. Further, addition of Cr in large quantities into the steel deteriorates the toughness of the base material of the steel and weld heat-affected zones (HAZ). Therefore, development of steel for line pipes excellent in the corrosion resistance to CO2 and having favorable low-temperature toughness and favorable field weldability is strongly demanded.
DISCLOSURE OF THE INVENTION
Accordingly, the principal object of the present invention is to a provide novel steel for line pipes which is greatly improved in the corrosion resistance to CO2 without deteriorating low-temperature toughness of the base material and the HAZ.
The object is achieved firstly by preparing a steel of which composition is, by weight ~, 0.02 to 0.09 2 ~ o 1 carbon, 0.5 or less silicon, 0.7 to 1.5 manganese, 0.03 or less phosphorus, 0.005 or less sulfur, 0.02 to 0.06 niobium, 0.5 to not more than 1.2 chromium, 0.005 to 0.03 titanium, 0.05 or less aluminum, 0.002 to 0.005 nitrogen, and the balance of iron and unavoidable impurities, and which satisfies the equation: 0.35 S C + (Mn + Cr + V)/5 +
(Ni + Cu)/15 S 0.48, and secondly by processing the steel in accordance with the following steps: heating a block of the steel to a temperature in a range of 1100C to 1250C, rolling the block at 950C or less and at 700C to 850C of a finish rolling temperature with a cumulatine rolling reduction of 40% or more, and air-cooling or accelerated cooling the rolled product. Thus, the desired steel product can be obtained.
Further, if necessary, one element or more selected from the group consisting of 0.01 to 0.08 V, 0.05 to 0.5 Ni, 0.05 to 0.5 Cu and 0.001 to 0.005 Ca can be added to the steel of the above mentioned composition.
The present invention will be hereinafter described in detail.
In order to improve the corrosion resistance to C2 and obtain excellent low-temperature toughness of the base material and the HAZ and excellent field weldability, it is necessary to select a particular chemical composition of the steel. For this reason, the Cr content is set at 0.5 to 1.2% in respect of the corrosion resistance. The Cr content is required to be 0.5% at least to obtain adequate corrosion resistance. However, too much Cr 2 ~
1 largely deteriorates the low-temperature toughness and the field weldability. Therefore, the upper limit is set at 1.2%.
When a considerable amount of Cr is added to the steel to improve the corrosion resistance, 0.02 to 0.09%
of C (carbon) and 0.7 to 1.5% of Mn are necessary for ensuring excellent low-temperature toughness and excellent weldability. The lower limits of C and Mn are minimum amounts for obtaining the required strength of the base material and welded joints and achieving the effects of precipitation hardening and grain refining of Nb and V when these elements are added to the steel. The upper limits are critical values for obtaining excellent low-temperature toughness and excellent field weldability (most preferable C and Mn contents are 0~03 to 0.06% and 0.8 to 1.2%, respectively).
Yet, it is insufficient to restrict the content of each element only. The following equation has to be satisfied: 0.35% S C + (Mn + Cr + V)/5 + (Ni + Cu)/15 0.48. This is because low-temperature toughness and weldability are determined by a total amount of chemical components including Cr. The lower limit of 0.35~ is a minimum amount for obtaining the required strength of the base material and welded ioints, and 0.48% is the upper limit for obtaining excellent low-temperature toughness and excellent weldability.
The steel of the invention contains 0.02 to 0.06% Nb and 0.005 to 0.03% Ti as essential elements.
2 ~ ~ ~J ~
1 Nb contributes to refining of grain size and precipitation hardening in controlled rolling, thus toughening the steel. By adding Ti to the steel, fine TiN are formed, and coarsening of y grains is suppressed during slab-reheating and welding, effectively improving the basematerial toughness and the HAZ toughness.
When a large amount of Cr is added to the steel, separations are inhibited on impact fracture surfaces of the control-rolled steel in Charpy test or the like, thereby deteriorating the low-temperature toughness.
Particularly in the steel of the present invention containing small amounts of C and Mn, therefore, addition of Nb and Ti was found to be essential in relation to obtaining the excellent low-temperature toughness.
The lower limits of Nb and Ti contents are minimum amounts for these elements to achieve their effects, and the upper limits are critical values of addition amounts not to deteriorate the HAZ toughness and the field weldability.
Reasons for restricting the amounts of the other elements will be described.
When Si is added excessively to the steel, the weldability and the HAZ toughness are lowered, and consequently, the upper limit is set at 0.5~. Deoxidation of the steel can be sufficiently performed by Ti alone, and it is not always necessary to add Si to the steel.
The reason why contents of impurities of P ~phosphorus) and S (sulfur) are set at 0.03% or less and 1 0.005% or less, respectively, in the steel of the invention is that the low-temperature toughness of the base material and the welded joints can be further improved as a result.
Reduction in the P content prevents inter-granular cracking, and reduction in the S content prevents the roughness from being deteriorated by MnS. Preferable P and S contents are 0.01% or less and 0.003% or less, respectively.
Although al is an element which the steel usually contains for deoxidation, it is not always necessary to add it to the steel because deoxidation can be effected by Ti or Si. When the Al content exceeds 0.05%. Non-metallic inclusions are increased to degrade cleanliness of the steel. Therefore, the upper limit is set at 0.05%.
Nitrogen (N) serves to form TiN and improve the toughness of the base material and the HAZ through the effect of suppressing the coarsening of ~ grains. The minimum content for this purpose is 0.002%. However, too much N causes deterioration of the HAZ toughness by solute nitrogen and slab surface defects, so that it is necessary to lower the upper limit to 0.005% or less.
Reasons for adding V, Ni, Cu and Ca to the steel will now be described.
A main object of further adding these elements to the base compositions is to improve the properties such as strength and toughness without spoiling excellent characteristics of the steel of the present invention.
Consequently, addition amounts of them have to be naturally restricted.
_ 7 _ 2~ 0 1 Vanadium (V) takes substantially the same effects as Nb such as improvement of the low-temperature toughness and increase in strength due to refinement of the micro-structure, increase in the strength owing to precipitation hardening, and so forth. However, excessive addition of V induces deteriorations of the weldability and the HAZ
toughness, and therefore, the upper limit is set at 0.08%.
Ni improves both the strength and the toughness without giving unfavorable influences to the wledability and the HAZ toughness, and it is also effective in prevention of hot cracks at the time of addition of Cu to the steel. However, the content exceeding 0.5% is not preferable economically, and accordingly, the upper limit is set at 0.5%.
Although Cu is effective in corrosion resistance and resistance against hydrogen induced cracking, the content exceeding 0.5% causes copper-cracks during hot rolling, resulting in difficulty in the manufacture of the steel. Therefore, the upper limit is set at 0.5%.
Calcium (Ca) controls the shape of a sulfide (MnS) and improves the low-temperature toughness (increase in Charpy absorption energy and the like), and it is also effective remarkably in improvement of the resistance against hydrogen-induced cracking. However, the Ca content not more than 0.001% has no effect in practice, and addition of Ca exceeding 0.005% induces generation of large amounts of CaO and CaS which become to coarse inclusions, not only degrading cleanliness of the steel - 8 - ~ 9 1 but also giving unfavorable influences to the toughness and the field weldability.
For this reason, the amount of Ca is limited to 0.001 to 0.005%. In order to improve the resistance against hydrogen-induced cracking, it is especially effective to reduce the sulfur (S) and oxygen (O~ contents to 0.001% or less and 0.002~ or less, respectively, and to satisfy the following equation: ESSP ' (Ca)[l - 124(0)]/1.25(S) 2 1.5. In this case, ESSP stands for Effective Sulfide Shape Controlling Parameter, and indicates a relation in the composition which prevents the sulfide from being extended in the rolling process.
More specifically, when the ESSP is set to 1.5 or more, the amount of MnS is reduced, and the amount of CaS, CaOS
which are not easily extended at the time of rolling is formed instead.
As for the above described steel containing Cr, an appropriate manufacturing method must be adopted to improve the low-temperature toughness of the base material, and it i8 necessary to restrict conditions of reheating, rolling and cooling of the steel (slabs).
First, the reheating temperature is restricted to a range of 1100 to 1250C. The reheating temperature has to be not less than 1100C to dissolve Nb precipitates into matrix and to obtain a finish rolling temperature as high as required. However, when the reheating temperature exceeds 1250C, austenitic ~Y) grains become to be considerably coarse, and can not be refined - 9 - 2~4 1 sufficiently even by rolling, so that excellent low-temperature toughness can not be obtained. Thus, the reheating temperature is set at not more than 1250C
(preferably, 1150 to 1200C).
Moreover, the cumulative rolling reduction at 950C or less must be set at not less than 40%, and the finish rolling temperature has to be set at 700 to 850C.
This is because ~ grains which have been refined by recrystallized region rolling are extended by low temperature rolling in the unrecrystallized region, so that resultant ferrite grain size is reduced to a minimum, thus improving the low temperature toughness. When the cumulative rolling reduction is under 40%, extending of the austenitic structure is insufficient, and therefore, fine ferritic grains can not be obtained.
Besides, when the finish rolling temperature is 850C or more, fine ferrite grains can not be obtained even if the cumulative rolling reduction is not less than 40~. However, when the finish rolling temperature is too low, it results in excessive two phase (~ + ~) of austenitic and ferritic phases region rolling, thus deteriorating the low temperature toughness. Therefore, the lower limit of the finish rolling temperature is set at 700C.
Air cooling or accelerated cooling is desirable for cooling after rolling. As a condition of the accelerated cooling, it is preferable to cool the steel to a desired temperature of not more than 600C at a -- 1 o -- 2 ~
1 cooling speed of 10 to 40C/sec immediately after cooling, and to air-cool it thereafter. The advantage of the present invention will not be lost even if the manufactured steel is reheated at a temperature not more than ACl point for the purpose of tempering, dehydrogenation and so forth.
EXAMPLES
Steel plates (15 to 32 mm thick) having various steel compositions were manufactured through converter process, continuous casting process and plate rolling process, and examined in respect of strength, toughness, low-temperature toughness and corroslon resistance.
Test items and results are shown in Table 1.
All of the steel plates (steels of the present invention) manufactured according to the invention method have favorable properties. On the other hand, comparative steels which were not manufactured according to the present invention are inferior in strength, low-temperature toùghness or corrosion resistance.
As for comparative steels 11 to 19, a steel 11 whose Cr content is low is inferior in the corrosion resistance. A steel 12 whose Cr content is excessive is inferior in the weldability, with Pc (= C + (Mn + Cr +
V)/5 + (Ni + Cu)/15) being high, and the HAZ toughness is also inferior. A steel 13 whose carbon content is high is inferior in the low-temperature toughness of both the base material and the HAZ. A steel 14 whose Mn content is - 11 2~
1 high is inferior in the HAZ toughness. A steel 15 contains no Nb so that the strength of the base material is low, and that the toughness is inferior as well. A steel 16 containing no Ti is inferior in the toughness of the base material and the HAZ. As for a steel 17, the reheating tempexature is low, and consequently, the base material strength is insufficient. A steel 18 is inferior in the base material toughness because the cumulative rolling reduction at 950C or less is insufficient. Further, a steel 19 whose finish rolling temperature is too low is inferior in the base material toughness.
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1 As will be apparent from the above, according to the present invention, there can be produced line pipes having improved corrosion resistance to C02 and high strength which are excellent in field weldability. As a result, efficiency of welding work in fields and safety of pipe lines are remarkably improved.
INDUSTRIAL APPLICABILITY
The steel manufactured according to the invention method is superior in low temperature toughness and corrosion resistance to C02, and it is also excellent in field weldability. It is suitable for large-diameter line pipes for transportation of oil or natural gas in cold regions and offshores.
Claims (3)
1. A manufacturing method of high corrosion-resistant low alloy steel for line pipes, comprising the steps of heating the low alloy steel at a temperature in a range of 1100°C to 1250°C, rolling the steel with the cumulative rolling reduction at 950°C or less being 40% or more, a finish rolling temperature of 700°C to 850°C, and air-cooling or acceleratedly cooling the low alloy steel after rolling, the steel comprising, by weight %, 0.02 to 0.09 carbon, 0.5 or less silicon, 0.7 to 1.5 manganese, 0.03 or less phosphorus, 0.005 or less sulfur, 0.02 to 0.06 niobium, 0.5 to not more than 1.2 chromium, 0.005 to 0.03 titanium, 0.05 or less aluminum, 0.002 to 0.005 nitrogen and the balance of iron and unavoidable impurities, and the low alloy steel satisfying the following equation:
0.35 ? C + (Mn + Cr + V)/5 + (Ni + Cu)/15 ? 0.48
0.35 ? C + (Mn + Cr + V)/5 + (Ni + Cu)/15 ? 0.48
2. A manufacturing method of high corrosion-resistant low-alloy steel for line pipes according to Claim 1, wherein the steel further comprises one element or more selected from the group consisting of 0.01 to 0.08 vanadium, 0.05 to 0.5 nickel, 0.05 to 0.5 copper, and 0.001 to 0.005 calcium, by weight %.
3. A manufacturing method of high corrosion-resistant low-alloy steel for line pipes according to Claim 2, wherein the steel satisfies the following equation: ESSP ? (Ca) (1 - 124 (oxygen))/1.25 (S).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP02-005263 | 1990-01-12 | ||
JP2005263A JP2711163B2 (en) | 1990-01-12 | 1990-01-12 | Method for producing high corrosion resistant low alloy linepipe steel with excellent corrosion resistance |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2049050A1 true CA2049050A1 (en) | 1991-07-13 |
Family
ID=11606343
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002049050A Abandoned CA2049050A1 (en) | 1990-01-12 | 1991-01-10 | Manufacturing method of high corrosion-resistant low-alloy steel for line pipes |
Country Status (6)
Country | Link |
---|---|
JP (1) | JP2711163B2 (en) |
CA (1) | CA2049050A1 (en) |
DE (2) | DE4190090T (en) |
GB (1) | GB2247246B (en) |
NO (1) | NO300552B1 (en) |
WO (1) | WO1991010752A1 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
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GB9206422D0 (en) | 1992-03-24 | 1992-05-06 | Bolt Sarah L | Antibody preparation |
US5723089A (en) * | 1994-03-11 | 1998-03-03 | Nippon Steel Corporation | Line pipe metal arc welded with wire alloy |
JP5381828B2 (en) * | 2010-03-15 | 2014-01-08 | 新日鐵住金株式会社 | Refractory steel material excellent in high-temperature strength of base metal and high-temperature ductility of weld heat-affected zone and its manufacturing method |
CN111118410A (en) * | 2020-01-16 | 2020-05-08 | 天津钢管制造有限公司 | Thick-wall large-caliber high-steel grade pipeline pipe with thickness of 40-60 mm and manufacturing method thereof |
CN112695246A (en) * | 2020-12-08 | 2021-04-23 | 中国石油天然气集团有限公司 | Acid corrosion resistant high-strength pipeline steel and manufacturing method thereof |
CN112921250B (en) * | 2021-01-25 | 2022-04-26 | 北京科技大学 | CO-resistant2Corroded steel pipe and preparation method thereof |
CN112941422B (en) * | 2021-01-25 | 2022-08-23 | 北京科技大学 | CO-resistant 2 Steel plate for corrosion and preparation method thereof |
CN116179958B (en) * | 2023-03-14 | 2024-08-23 | 北京科技大学 | Ni, cr and Cu composite regulation low-alloy stress corrosion resistant anchor cable steel and preparation method thereof and anchor cable |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1084310A (en) * | 1976-04-12 | 1980-08-26 | Hiroaki Masui | High tension steel sheet product |
JPS5814848B2 (en) * | 1979-03-30 | 1983-03-22 | 新日本製鐵株式会社 | Manufacturing method of non-tempered high-strength, high-toughness steel |
JPS62112722A (en) * | 1985-11-13 | 1987-05-23 | Nippon Steel Corp | Production of steel sheet having excellent resistance to hydrogen induced cracking and resistance to sulfide stress corrosion cracking |
JPS6338520A (en) * | 1986-08-01 | 1988-02-19 | Sumitomo Metal Ind Ltd | Method for producing steel sheets with excellent hydrogen-induced cracking resistance |
DE3832014C2 (en) * | 1988-09-16 | 1994-11-24 | Mannesmann Ag | Process for the production of high-strength seamless steel tubes |
-
1990
- 1990-01-12 JP JP2005263A patent/JP2711163B2/en not_active Expired - Lifetime
-
1991
- 1991-01-10 CA CA002049050A patent/CA2049050A1/en not_active Abandoned
- 1991-01-10 WO PCT/JP1991/000010 patent/WO1991010752A1/en active Application Filing
- 1991-01-10 DE DE19914190090 patent/DE4190090T/de active Pending
- 1991-01-10 DE DE4190090A patent/DE4190090C2/en not_active Expired - Lifetime
- 1991-09-10 GB GB9119268A patent/GB2247246B/en not_active Expired - Lifetime
- 1991-09-11 NO NO913584A patent/NO300552B1/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
NO913584L (en) | 1991-09-11 |
NO913584D0 (en) | 1991-09-11 |
JPH03211230A (en) | 1991-09-17 |
GB9119268D0 (en) | 1991-11-20 |
DE4190090T (en) | 1992-01-30 |
JP2711163B2 (en) | 1998-02-10 |
GB2247246B (en) | 1994-05-11 |
DE4190090C2 (en) | 1996-09-05 |
GB2247246A (en) | 1992-02-26 |
WO1991010752A1 (en) | 1991-07-25 |
NO300552B1 (en) | 1997-06-16 |
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