KR100825632B1 - Ferritic stainless steel having excellent formability of welded zone and corrosion resistance, and method for manufacturing the same - Google Patents

Abstract

Provided are ferritic stainless steels excellent in workability of welds and corrosion resistance of steels, and methods for manufacturing the same.

The ferritic stainless steel is mass%, C: 0.01% or less, N: 0.01% or less, Si: 1.0% or less, Mn: 1.0% or less, Cr: 10.0 to 20.0%, Al: 0.15% or less, Ca: 0.0005 ~ 0.002%, Zr: 0.0018 ~ 0.01%, O: 0.004 ~ 0.008%, Ti: 0.01 ~ 0.5%, remaining Fe and other unavoidable impurities. Moreover, the manufacturing method of this ferritic stainless steel is provided.

The ferritic stainless steel of the present invention refines the solidification crystal grains of the welded portion by the complex addition of Ca and Zr, thereby improving the workability of the welded portion, and also improving the corrosion resistance of the steel.

Ferritic Stainless Steel, Corrosion Resistance, Secondary Machinability, Ca-Zr Oxide

Description

Ferritic stainless steel having excellent formability of welded zone and corrosion resistance, and method for manufacturing the same}

Iron and Steel (Vol. 66, 1980, 110p)

2. Japanese Laid-Open Patent Publication 1997-125209

3. JP 2000-160299

4. JP-A 1997-217151

5. Japanese Laid-Open Patent Publication 1997-271900

6. JP-A-1998-324956

7. JP 2001-020046

8. JP 2001-181808 A

9. Japanese Patent Application Laid-Open No. 2001-288543

10. Japanese Laid-Open Patent Publication 2001-294991

11. Japanese Laid-Open Patent Publication 2002-285292

12. Japanese Laid-Open Patent Publication 2002-336990

13. Japanese Laid-Open Patent Publication 2003-221652

The present invention relates to a material excellent in workability of the welded portion and corrosion resistance of the steel, and more particularly, to improve the corrosion resistance by controlling the component and size of the oxide of the steel, and further solidifying crystal grains of the welded portion by using the coagulation nucleation action of the oxide The present invention relates to a ferritic stainless steel capable of improving the workability of a welded part by miniaturizing it.

Recently, the automobile industry is required to improve fuel efficiency by tightening and reducing exhaust gas regulations, and automobile manufacturers are adopting ferritic stainless steel having excellent heat resistance and corrosion resistance in place of existing castings or aluminum plated steel sheets.

Exhaust system parts are largely composed of a shell and a pipe, and are mostly manufactured and assembled by welding. Therefore, it can be said that securing the quality characteristics of the welded portion is a very important factor that determines the performance of the exhaust system components. As an example, the exhaust system material is a steel sheet or a welding pipe (pipe manufactured by a method such as high frequency welding, TIG welding, laser welding, etc.) into a predetermined shape, and then welded again to produce a product. Since the shape of the exhaust system is quite complicated, during forming, the steel sheet or pipe is subjected to harsh processing. The ferritic stainless steel pipe material has a crack in the weld metal or weld heat affected zone when secondary processing such as bending or expansion is applied to the welded part. In many cases, the excellent workability cannot be exhibited. This phenomenon is remarkably caused by brittle cracks in the pipe welds when forming in winter or at low processing temperatures.

According to the prior art, there are four main factors that reduce the workability of welded parts, such as residual stress during hardening, hardening, coarsening of impurity elements such as C and N, and coagulation grains. As a method of reducing the residual stress, it is most effective to anneal the entire pipe to remove the deformation amount near the welded portion. Japanese Laid-Open Patent Publication No. 1997-125209 discloses a method of annealing a pipe manufactured by welding at a temperature range of 850 to 1000 ° C and cooling at a cooling rate of 1 ° C / sec or more. According to this method, it is reported that the workability and toughness of the pipe can be improved to the extent of the cold rolled annealing plate. However, when annealing is performed, an increase in the manufacturing cost is inevitable, and in the case of a high alloyed pipe for securing high heat resistance and oxidation resistance, sufficient quality characteristics cannot be secured by annealing.

The hardening phenomenon of the weld is closely related to the amount of alloying elements such as Si, Mn, Ti, Nb and the like, and the amount of impurity elements such as C and N. In the case of alloying elements, it is often difficult to control the content as a basic element for exhibiting the manufacturing process and the characteristics of the product. Therefore, a method of reducing the amount of C and N, which are impurity elements, is being actively developed and applied. Impurities C and N are known to form nitrides or carbides by adding elements such as Ti, Nb and Zr as stabilizing elements together with improvements in steelmaking processes such as VOD (Vacuum Oxidation Decaburizaton) refining techniques. At present, the amount of C + N in the VOD process is about 100 ppm, and the increase in productivity and manufacturing cost due to the addition of the steelmaking process is pointed out as a problem. To reduce the amount of solid solution C and N by forming nitrides or carbides by adding stabilizing elements such as Ti, Nb, and Zr, it is basically added at least 8 times of C + N. In some cases.

However, when a large amount of Ti is added, coarse oxidized inclusions or precipitates are formed to easily cause surface cracks and rolling defects during rolling, and Zr causes nozzle clogging during steelmaking. It is shown. In addition, in the case of rapid heat quenching such as a welded part, since the time required for the formation of precipitates is extremely short, even if the content of Ti, Nb, Zr is simply increased, sufficient precipitates cannot be formed, but rather Ti, Nb, Zr and The amount of C, N, etc. increases, so workability may not be secured.

On the other hand, methods for improving the workability by miniaturizing the solidification structure of the steel and weld metal parts have been recently proposed. The method of controlling the coagulation structure can be largely classified into techniques for improving ferrite nucleation of inclusions by improving the equipment and adding alloying elements such as electromagnetic induction stirring of molten steel (Vol. 66, No. 6, 1980, page 38). have. In the case of the method by electromagnetic induction stirring, it is known that the equiaxed crystallization rate of about 40 to 60% of the steel is secured by optimizing the stirring position of the molten steel during the solidification. The above technique can improve the machinability of the steel, but it is pointed out that a problem cannot be obtained when remelting the steel such as welding.

The microstructure of the coagulation structure using inclusions is known to use TiN (No. 1 and 2) precipitates and oxides (No. 3 and 10). In the following description, (%) represents wt%.

1. Iron and steel (Vol. 66, 1980, 110p): A method of producing TiN by containing 0.4% Ti and 0.016% N in steel and managing molten steel superheat degree below 40 ℃.

2. JP2000-160299: A technique for securing an equiaxed crystallization rate of 60% in the slab phase, containing 0.01% or more of TiN inclusions alone.

3. JP1997-217151, JP1997-271900: A technique for miniaturizing the solidification structure of a weld by adding Mg-Al composite oxide by adding 0.001-0.02% Mg and 0.001-0.2% Al, respectively.

4.JP1998-324956: After deoxidizing the amount of oxygen to 0.01% or less in molten steel, Mg is added at 0.0005 ~ 0.01% and the solidification starts within 180 seconds. contained in steel in a distribution of mm ² .

5. JP2001-020046: A composite inclusion of Mg-Al-based oxide and Ti-based nitride was formed by setting the content ratio of Mg and Al in steel to 0.3 to 0.5.

6. JP2001-181808: Method of improving workability of materials without adding cold rolling by adding 0.0005 ~ 0.01% Mg, minimizing coagulation structure with Mg inclusions and optimizing hot rolling conditions.

7. JP2001-288543: A method for improving the coagulation grains of steel and improving the workability, surface properties and corrosion resistance by adding Mg and Ca content of 0.006% or less.

8. JP2001-294991: Composite inclusions of Mg-based oxides and TiN precipitates contained in the steel with a distribution of 0.01 to 5 mm, 3 / mm ² or more.

9. JP2002-285292: Add 0.001 ~ 0.05% of rare earth metal Y to form inclusions such as Al-Y, Mg-Y, Al-Mg-Y and refine solidification crystal grains in steel sheet manufacturing process and steel pipe manufacturing process How to prevent brittle cracks.

10.JP2002-336990: Add 0.01 ~ 0.3% Ti and 0.01 ~ 0.2% Al, and use Ti, Al-based nitride in welding metal more than 0.3mm by using Ar, O ₂ , CO ₂ , He, etc. How to distribute more than 1.5 × 10 ⁴ / mm ² .

11.JP2003-221652: Contains 0.0003 ~ 0.003% Ca and 0.01% or less of O, controls the content of O and S in the range of S / 1.25 + O / 5≥0.003, and optionally adds Zr by 0.01 ~ 0.3% Thereby forming CaS or CaO oxide in the steel and promoting the nucleation role of the ferrite (111) plane during hot rolling.

In the above technique, Nos. 1 and 2 are used to refine TiN in the molten metal to refine the solidification structure of the steel slab, but it is difficult to apply when the temperature control of the molten metal is difficult, such as welding, and a large amount of Ti and TiN impairs the toughness of the steel. Therefore, there is a possibility that the problem of brittle cracking of ferritic stainless steel is further exacerbated.

Known techniques 3 to 10 are methods to promote the coagulation nucleation by forming oxides in molten metal by adding Mg, Y, etc. alone or in combination, but it is difficult to predict the recovery rate when Mg, Y, etc. having excellent oxidation reactivity are added to molten steel. Therefore, quality deviations by steel materials frequently occur, and there are problems in handling such as explosiveness.

Known technology No. 11 is a method of producing CaS and CaO in molten steel and promoting the production of ferrite (111) plane having excellent workability during hot rolling. However, this is a technique of adding Zr after loading Ca and then adding Zr to remove residual oxygen to form coarse oxidation inclusions or sulfides. Such coarse inclusions lower the surface quality of the steel and cause corrosion resistance due to the increase in the interfacial area between the inclusions and the matrix, and also increase the manufacturing cost due to the addition of a large amount of Zr.

As such, there is a need for a ferritic stainless steel that can secure weldability of steel and at the same time ensure corrosion resistance, but no alternative has been proposed.

An object of the present invention is to provide a ferritic stainless steel excellent in workability of the welded portion and corrosion resistance of the steel material and a method for producing the same.

Ferritic stainless steel of the present invention for achieving the above object is by mass%, C: 0.01% or less, N: 0.01% or less, Si: 1.0% or less, Mn: 1.0% or less, Cr: 10.0-20.0%, Al : 0.15% or less, Ca: 0.0005 ~ 0.002%, Zr: 0.0018 ~ 0.01%, O: 0.004 ~ 0.008%, Ti: 0.01 ~ 0.5%, remaining Fe and other unavoidable impurities.

In addition, the method of manufacturing a ferritic stainless steel of the present invention comprises the steps of manufacturing a stainless molten metal in an electric furnace, refining the prepared stainless molten metal, continuous casting the refined molten metal, rolling the cast ingot, Manufactured by the step of annealing the rolled rolled material,

By mass%, C: 0.01% or less, N: 0.01% or less, Si: 1.0% or less, Mn: 1.0% or less, Cr: 10.0 to 20.0%, Al: 0.15% or less, Ca: 0.0005 to 0.002%, Zr: 0.0018 ~ 0.01%, O: 0.004 ~ 0.008%, Ti: 0.01 ~ 0.5%, remaining Fe and other inevitable impurities,

The refining step includes controlling the oxygen to 0.01% or less, and then charging Zr into the molten metal and then charging Ca.

Hereinafter, the present invention will be described in detail.

The present invention is characterized in that the solidified crystal grains of the weld portion is refined in order to improve the low-temperature workability and corrosion resistance of the ferritic stainless steel weld portion, to form a sufficient carbonitride to reduce the amount of residual C and N.

Hereinafter, the reason for component limitation of the ferritic stainless steel of this invention is demonstrated.

C, N: Since C and N are elements that degrade the workability of the base metal and the welded part, it is preferable to use them in the smallest amount possible. However, C: 0.01% or less and N: 0.01% or less in consideration of the increase in manufacturing cost in steelmaking technology. .

Si, Mn, Al, P, S: These elements are invariably present in steel, but when present in a large amount, they lower workability and lower corrosion resistance, which is characteristic of stainless steel, Si: 1.0% or less, Mn: 1.0% or less , Al: 0.15% or less, P: 0.040% or less, S: 0.010% or less is appropriate.

Cr: Cr is less than 10% and the amount of Cr is 10% or more because the corrosion resistance, which is the basic characteristic of stainless steel, is insufficient. If the Cr content is high, the toughness of the weld section may deteriorate, so the Cr content is 20% or less.

Ca: Ca is an essential element for improving the weldability which becomes a subject in this invention. In order to improve weldability, addition of 0.0005% or more is required. However, if it is added in excess of 0.002%, the upper limit is set to 0.002% because the size of the oxidation inclusion increases and adversely affects the corrosion resistance.

Zr: Zr is an essential element for improving the weldability which becomes a subject in this invention like Ca. In addition, Zr serves to improve the corrosion resistance of steel by minimizing the size of oxide particles. Zr also forms nitrides or carbides to form complexes with oxides. In order to improve weldability and corrosion resistance, addition of 0.002% or more is required. However, if it is added in excess of 0.01%, there is a problem such as cost increase due to the addition amount and nozzle clogging during the steelmaking process, so the upper limit is 0.01%.

O: Zr, Ca-based oxides, the oxide is difficult to form if less than 0.004%, it was confirmed that the effect of improving the quality is less than 0.008%. If the workability of the weld is extremely demanded, the oxygen content is preferably 0.005% or less.

Ti: It adds as an element which improves workability. Ti: The effect is exhibited by adding 0.01% or more. However, when Ti is added in excess of 0.5%, there is a problem in that workability deteriorates due to an increase in the amount of solid solution Ti.

The alloying element may be included according to the properties required for the steel formed from the above component system. For example, in order to improve corrosion resistance, at least one of Mo, Ni, and Cu may be further added in a composition range of 0.1-2.0%. When the content of at least one of Mo, Ni, and Cu is 0.1% or more, the effect of improving corrosion resistance can be obtained. If the content exceeds 2.0%, the workability is deteriorated and the manufacturing price is increased. In addition, Nb may be included up to 0.5%. If the content of Nb exceeds 0.5%, there is a problem that the workability deteriorates due to the increase in the amount of solid solution Nb. When Nb is added to form NbN, NbC, or the like to improve workability, it is preferably included as 0.01-0.5%.

In the steel satisfying the composition range according to the present invention, Ca-Zr-based or Ca-Zr-Ti-based oxides are present. It is preferable that these oxides contain 5-10 piece / mm <2> in 1-3 micrometers size. Ti-based or Nb-based precipitates of 1 µm or less contain 39,000 particles / mm 2 or more.

The manufacturing method of the steel of this invention is demonstrated.

Ferritic stainless steel of the present invention described above is manufactured through the following process. First, a molten stainless steel is produced in an electric furnace, and the molten stainless steel is refined. Then, the refined molten metal is continuously cast to obtain a steel ingot, and the steel ingot is rolled to obtain a rolled material. This rolled material is annealed.

In the present invention, in order to obtain the desired Ca-Zr, Ca-Zr-Ti-based oxide, oxygen is controlled to 0.01% or less in the refining step, and then Zr is added to the molten metal and then charged with Ca. Conventionally, there is a technique of removing residual oxygen by adding Zr after charging Ca and then adding Zr. In this case, coarse CaO or CaS is formed, which results in deterioration of steel surface quality and corrosion resistance, and is manufactured by adding a large amount of Zr. There was a problem that the unit price increased.

When Ca and oxygen react with each other to form CaO alone, the size of the oxide is excessive, which causes the above problem. In the case of ZrO, the size of ZrO is small and cannot act as a solidification nucleus. Therefore, an object of the present invention is to form a complex oxide of Ca and Zr to control the size of the oxide to a suitable size to act as a coagulation nucleus.

However, in the case of Ca, since the reactivity with oxygen is greater than that of Zr, when Ca is added first and then when Zr is added later or simultaneously, a large amount of Zr must be added in order to achieve the same effect as the present invention. Due to the large amount of ZrO, ZrN generated by the brittle crack and problems of unit cost rise.

In the present invention, Zr is added before Ca injection. When a small amount of Zr is pre-injected, ZrO is formed to lower the concentration of oxygen, and then Ca is added to form a complex oxide with Zr to optimize the size of the oxide to improve workability and corrosion resistance.

In addition, Ti reacts with nitrogen to form TiN, thereby lowering the nitrogen concentration to improve processability. Ti is added before the refining step, but before Ca and Zr, but in the case of TiN, the melting point is lower than that of Ca-Zr-based or Ca-Zr-Ti-based oxides, and then Ca-Zr-based or Ca-Zr-Ti-based oxides are formed. TiN is formed around a part of the composite oxide to form a composite inclusion. In the case of Nb, nitride is formed in the same manner as Ti to form a composite inclusion with Ca-Zr-based or Ca-Zr-Ti-based oxide, so that it can be selectively or combined with Ti.

In the case of the oxide and the composite inclusion, since the melting point is high, the present invention is particularly effective in improving the workability and corrosion resistance of the welded part because it exists in the newly solidified tissue and acts as a solidification nucleus even when it is formed in the molten stage and then welded again. .

Ti-based or Nb-based precipitates: Ti or Nb reacts with carbon in the molten metal to form precipitates in the form of TiC or NbC to improve workability. The main component of the precipitate may be carbides or some nitrides.

An example of the refining method according to the present invention is shown in Table 1 below.

Input order Nitride oxide Precipitate Composite inclusions Ti → Ca → Zr TiN CaO, ZrO TiC none Ti → Zr → Ca TiN Ca-Zr or Ca-Zr-Ti Composite Oxide TiC Ca-Zr-based or Ca-Zr-Ti-based oxide and nitride complex

When Ca is added before Zr in Table 1, since the reactivity with oxygen is greater than that of Zr, an oxide of a single form of CaO and ZrO is formed. On the other hand, when Zr is added before Ca is added, a complex oxide such as Ca-Zr system is formed. In this case, the recovery rate of Zr is improved.

In the present invention, weldability is improved by any method as long as it is a welding method via a melt-solidification process such as GTA welding, laser welding, or plasma welding regardless of the welding method. Welding conditions may be selected corresponding to various conditions such as the material composition, steel sheet thickness, purpose.

Hereinafter, the present invention will be described in detail with reference to the following examples, which are only preferred embodiments of the present invention, and the scope of the present invention is not limited by the description of these embodiments.

(Example)

Ten types of ferritic stainless steels shown in Table 2 were dissolved, and a 1.5 mm thick plate was produced by hot rolling, annealing, pickling, cold rolling, annealing, and pickling, and GTA welding was performed. No. 1 shows the basic alloy composition of STS409L, Nos. 2 to 3 are added to Ca alone, and Nos. 4 to 9 show the combined addition of Ca and Zr when the C + N content is changed. No10 is a comparative example when the amount of oxygen is not controlled. In the case of Nb, 0.014% in Example 4, 0.012% in Example 9, and 0.013% in the other examples.

Test Solution Ferritic Stainless Steel Chemical Composition (wt%) No C N O Si Mn P S Cr Ti Zr Ca One 0.006 0.006 0.0053 0.45 0.30 0.01 0.002 11.3 0.23 - - 2 0.006 0.006 0.0056 0.45 0.31 0.01 0.002 11.3 0.23 - 0.0009 3 0.006 0.006 0.005 0.45 0.30 0.01 0.002 11.3 0.23 - 0.0014 4 <0.005 0.0067 0.005 0.518 0.326 0.01 <0.002 11.25 0.21 0.0018 0.0009 5 <0.005 0.0067 0.005 0.485 0.281 0.01 <0.002 11.41 0.26 0.0022 0.0007 6 <0.005 0.0060 0.005 0.443 0.291 0.01 <0.002 11.39 0.256 0.0050 0.0010 7 0.008 0.010 0.005 0.459 0.303 0.01 <0.002 11.31 0.238 0.0025 0.0012 8 0.007 0.0088 0.005 0.472 0.295 0.01 <0.002 11.32 0.233 0.0046 0.0014 9 0.006 0.0099 0.005 0.440 0.295 0.01 <0.002 11.34 0.233 0.009 0.0015 10 <0.005 0.0060 0.011 0.480 0.290 0.01 <0.002 11.31 0.253 0.0025 0.0012

The manufacturing method of the present invention comprises the steps of producing a stainless molten metal in an electric furnace of the composition, refining the prepared stainless molten metal, continuous casting the refined molten metal, rolling the cast ingot, It is prepared by the step of annealing the rolled steel ingot,

The refining step included controlling oxygen to O: 0.004% to 0.008% and charging Zr to the molten metal immediately before continuous casting.

The control of oxygen was carried out with Si or Al deoxidizer in the AOD or VOD step, and Ca and Zr are volatile, so there is a problem that the amount remaining in the electric furnace process or the AOD or VOD process is reduced. Was put in. Ca is Fe-Ca-based, Zr is a pure metal plate.

GTA welding was performed using a DC type welding machine (maximum welding current 350A), and a bead on plate. Welding conditions were welding current: 110A, welding speed: 0.32m / min, tungsten electrode diameter: 2.5mm, electrode tip angle: 100 °, Arc length 1.5mm, protective gas Ar (15l / min).

Grain size of the weld was measured using an optical microscope. Weld sections were polished using sandpaper and abrasive, and observed after electroetching with a Nital solution. The hardness distribution of the welded part was measured using a MicroVickers hardness tester with a load of 200 g and a holding time of 10 s at 0.2 mm intervals.

The method for measuring the distribution of oxide and precipitate particles is to measure the number and size of specularly polished test specimens in EPMA for the size of 1 μm or more by mapping the elements forming the oxides and precipitates at 5000 times 10 o'clock, Calculated. Further, oxides and precipitates of particles smaller than 1 μm were suspended on a mesh and analyzed using a transmission electron microscope at 100,000 to 100,000 fields.

The DBTT characteristics of the weld were investigated by applying the Charpy impact test on a 1/4 Sub-size (1.5mmt × 10mmw × 55mml) test specimen in the test temperature range of -60 ~ 100 ℃. . The official test was to polish the Ø15 disc specimens with sandpaper # 600, and then leave it in air for at least 5 hours to form a passivation film.

Table 3 shows the results of evaluating the impact characteristics of the weld and the corrosion resistance of the steel for 10 test specimens. Examples 4 to 9, which are inventive examples, show that the grain size and hardness of the welded portion are reduced, and the DBTT characteristics and impact energy variation of the welded portion are reduced when Ca and Zr are added in combination with the additives and the Ca added additives of Examples 1 to 3. It became. In addition, in the case of Ca + Zr additive, the official potential value is also increased, it can be seen that the corrosion resistance of the steel can be improved at the same time. In particular, when Ca and Zr are added in combination, low temperature impact characteristics and corrosion resistance of steel can be secured even at 180ppm of C and N contents, and thus, the operation time of the refining process can be shortened. do. In addition, the invention example in which the oxygen concentration was controlled to 0.01% or less improved weldability and corrosion resistance than Example 10, in which the oxygen concentration was not controlled.

As described above, the ferritic stainless steel of the present invention is improved by the addition of Ca and Zr to refine the solidified crystal grains of the weld to improve the workability of the weld, and can provide a ferritic stainless steel excellent in corrosion resistance of the steel. It works.

Claims (8)

By mass%, C: 0.01% or less, N: 0.01% or less, Si: 1.0% or less, Mn: 1.0% or less, Cr: 10.0 to 20.0%, Al: 0.15% or less, Ca: 0.0005 to 0.002%, Zr: 0.002 ~ 0.01%, O: 0.004 ~ 0.008%, Ti: 0.01 ~ 0.5%, remaining Fe and other unavoidable impurities. A ferritic stainless steel having excellent workability of welded parts and corrosion resistance of steel, comprising Ca-Zr-based oxide and Ti-based precipitate including Ca-Zr-Ti-based oxide. delete delete The method of claim 1, wherein the stainless steel is composed of Ca-Zr-based or Ca-Zr-Ti-based oxide of 1 to 3㎛ size 5-10 pieces / mm2, and the Ti-based precipitates of less than 1㎛ 39,000 pieces / Processability of the welded part characterized in that it comprises at least 2 mm 2 The ferritic stainless steel of claim 1, wherein when the welding is applied, the weld grain has a grain size of 300 μm or less, and the weld portion has a hardness of 145 Hv or less. Manufacturing a molten stainless steel in an electric furnace, refining the molten stainless steel, continuously casting the refined molten metal, rolling the cast ingot, and annealing the rolled rolled material. , By mass%, C: 0.01% or less, N: 0.01% or less, Si: 1.0% or less, Mn: 1.0% or less, Cr: 10.0 to 20.0%, Al: 0.15% or less, Ca: 0.0005 to 0.002%, Zr: 0.002 ~ 0.01%, O: 0.004 ~ 0.008%, Ti: 0.01 ~ 0.5%, stainless steel composed of remaining Fe and other unavoidable impurities, The refining step includes forming Ca-Zr-based oxides and Ti-based precipitates including Ca-Zr-Ti-based oxides by controlling oxygen to 0.01% or less and then adding Zr to the molten metal and then charging Ca. Method for producing a ferritic stainless steel excellent in workability of the weld and corrosion resistance of the steel. 7. The method of claim 6, wherein the stainless steel has a Ca-Zr-based or Ca-Zr-Ti-based oxide having a size of 1 to 3 µm or more than 5 / mm 2 and less than 1 µm when welding is applied. A Ti-based precipitate comprising 39,000 pieces / mm 2 or more, the manufacturing method of ferritic stainless steel excellent in the workability of a welded part and corrosion resistance of steel materials. The method for manufacturing ferritic stainless steel according to claim 6, wherein the stainless steel has a grain size of 300 μm or less and weld hardness of 145 Hv or less when welding is applied.