US3661658A - High-strength and high-toughness cast steel for propellers and method for making propellers of said cast steel - Google Patents

High-strength and high-toughness cast steel for propellers and method for making propellers of said cast steel Download PDF

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US3661658A
US3661658A US864898A US3661658DA US3661658A US 3661658 A US3661658 A US 3661658A US 864898 A US864898 A US 864898A US 3661658D A US3661658D A US 3661658DA US 3661658 A US3661658 A US 3661658A
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cast steel
casting
propellers
propeller
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Teishiro Oda
Makoto Nakamura
Masato Zama
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Mitsubishi Heavy Industries Ltd
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/22Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/50Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for welded joints
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/30Ferrous alloys, e.g. steel alloys containing chromium with cobalt
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49316Impeller making
    • Y10T29/49332Propeller making
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/12All metal or with adjacent metals
    • Y10T428/12493Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12771Transition metal-base component
    • Y10T428/12861Group VIII or IB metal-base component
    • Y10T428/12951Fe-base component
    • Y10T428/12958Next to Fe-base component
    • Y10T428/12965Both containing 0.01-1.7% carbon [i.e., steel]

Definitions

  • ABSTRACT A method of making a high strength, high toughness cast steel marine propeller comprised of not more than 0.25 percent of carbon, not more than 1 percent of silicon, not more than 3 percent of manganese, from 5-20 percent of chromium, from l-8 percent of cobalt, and from 0.5-7 percent of one or both of molybdenum and tungsten, and the remainder consisting of iron.
  • the cast steel may contain up to 8 percent of nickel and up to 4 percent of copper, depending on the conditions.
  • the method comprises casting the propeller into individual sections, welding said sections together, heating to a temperature of 800 to l,000 C. and air cooling.
  • the propeller can be aged by heating to a temperature between 450 and 700 C. If desired, the individual cast sections can be annealed prior to welding.
  • an iron-base material i.e., cast steel
  • cast steel has been less frequently used as the propeller material, since its corrosion resistance against sea water as one of the requirements for propeller material is far inferior to copper alloys.
  • Another reason why cast steel has not been widely used as a propeller material is that its mechanical properties have not been necessarily excellent as compared with conventional copper alloys.
  • This invention is to provide an inexpensive high-strength and high-toughness cast steel especially suitable for the marine propeller material possessing a good combination of strength, hardness, ductility and toughness and weldability.
  • This cast steel is expected to be put into service under the condition of electric (cathodic) protection to prevent it from being corroded by sea-water. In that condition, the high hardness ensures a good erosion resistance.
  • the cast steel of this invention is characterized by containing less than 0.25 percent carbon, less than 1.0 percent silicon, less than 3.0 percent manganese, 5 to 20 percent chromium, l to 8 percent cobalt, one or both of molybdenum and tungsten from 0.5 to 7 percent, the rest consisting of iron and other impurities. Further the cast steel of this invention is characterized by less than 8 percent nickel and less than 4 percent copper, besides the above-mentioned constituents, may be added independently or in combination.
  • the method of making propellers of cast steel of the composition set forth above comprises the steps of after casting the propeller slowly cooling it at a rate of not more than 1" C. per minute, reheating the casting to between 800 and l,000 C.
  • the method of fonning the propeller includes the steps of welding the individual sections, heat treating the welded casting at 800-l,000 C. and then slowly cooling the casting at a rate of not more than 1 C. per minute. Further, whether the casting is formed as a single unit or from individual sections, the method includes the step of annealing at 630700 C.
  • the cast steel of this invention is for the most part facecentered cubic austenite matrix at sufficiently high temperatures, and when it is cooled from the above condition to room temperature, most of the matrix changes to body-centered cubic ferrite or martensite, and yields precipitates of intermetallic compounds mainly consisting of the intermetallic compound of moldybdenum or tungsten, when the body-centered cubic lattic matrix is again heated to a temperature between 450 and 700 C.
  • the purpose for precipitating the intermetallic compounds of molybdenum or tungsten is that, if the cast steel is reinforced by these intermetallic compounds, ductility and toughness of this cast steel can be maintained up to higher strength than those of-conventional cast steels reinforced by carbides.
  • this invention is designed to make the most of this fact; accordingly, the cast steel of this invention is entirely different in the essence from others although it has a chemical composition similar to some of conventional materials.
  • composition of the cast steel of this invention is determined by the reasons explained as follows:
  • Chromium The lower limit of its content is 5 percent, because if the chromium content is lower, the corrosion resistance is poor and not proper for use in sea water even when the cathodic protection against corrosion is applied. Further, if the chromium content exceeds 20 percent, the ferrite which does not disappear at high temperature, i.e., 8-ferrite, increases in its ratio to make the steel brittle, or the Ms-point is lowered to lose the strength of the steel because of the consequent increase of retained austenite. The upper limit of chromium content is thus determined to be 20 percent.
  • Cobalt The lower limit of cobalt is determined to be 1 percent, because it desirably prevents the formation of 8-ferrite and promotes the precipitation hardening by the mutual action with molybdenum. However, excessive addition of cobalt makes this steel less economical because of its high price, thus the upper limit of cobalt content has been determined to be 8 percent.
  • Molybdenum and tungsten are required to be added to this steel in the amount of at least 0.5 percent, because the cast steel of this invention takes advantage of the precipitation hardening by molybdenum and tungsten; the contents of more than 7 percent of molybdenum or tungsten make the steel less economical because of the cost of the two metals and lower ductility and toughness of the steel although it increases the strength. Considering these effects, the lower and upper limits of the content of the two metals are determined to be 0.5 and 7 percent, respectively.
  • Nickel content of less than 8 percent is established for the reason that, while the content of chromium, cobalt, melybdenum, etc., in the cast steel of this invention may be changed in accordance with the applied purpose, an austenite-forming element or nickel is added for adjustment so long as its addition does not make the steel much less economical when the suppressing of S-ferrite formation is necessary to prevent the reduction of ductility and toughness.
  • Copper of less than 4 percent is added considering that in the cast steel of this invention copper does not have markedly unfavorable influence on its mechanical propertiesbut has rather a favorable effect on the corrosion resistance. However, it is expected in the cast steel of this invention that the corrosion by sea water is prevented by means of cathodic protection, and so the addition of copper is not necessarily required.
  • Carbon content is limited to less than 0.25 percent; it is desirable from the viewpoint of the mechanical property and the weldability of the cast steel of this invention that the carbon content is as little as possible; however, too low a content of carbon makes melting difficult and the steel less economical, since high quality raw material becomes necessary.
  • the content limit of carbon is set in the range where the mechanical property and weldability of this cast steel are not markedly impaired. Silicon and manganese are necessary for deoxidation and their contents are permitted in accordance with common knowledge for the steels of this type. The content of manganese is somewhat higher than that of silicon, because of our consideration that manganese can substitute for nickel as an austenite-forming element.
  • the cast steel of this invention contains common impurities such as phosphorus and sulphur which inevitably enter intothe metal on melting; it is however, desirable to remove those impurities as much as possible so long as these impurities can be removed without any marked increase in cost.
  • the cast steel of this invention of which-the composition is defined for the above-mentioned reasons exhibits tensile strength from 60 to or more than 120 kg/mm, sufficiently high ductility and toughness in the as-cast condition if it is cooled at a sufficiently slow rate after casting. If the cooling rate is sufficiently high, the ductility and toughness decreases considerably. However, in this case, these propertiescan be improved by heating it to an appropriate temperature-above 900 C and then cooling it slowly. Even the material which has been cooled gradually at a sufiiciently slow cooling velocity can further improve its ductility and toughness after it is reheated.
  • the cast steel of this invention may be used more effectively as propeller material if the surface property is improved by taking advantage of the above-mentioned property of this material in such a manner that the surface is rapidly heated and rapidly cooled by such a method as high-frequency induction heating and then aged.
  • the cast steel of this invention exhibits excellent properties as the material for a marine propeller.
  • Table 1 shows typical examples of the compositions of cast steels of this invention. Each of samples was melted in a kg and a 500 kg high-frequency melting furnace and also in a 3-ton electric-arc melting furnace, and was cast into a sand mold. The cooling velocity after casting was controlled in a heat-treating furnace. Table 2 indicates mechanical properties as well as heat-treatment conditions of the materials whose compositions are listed in Table 1.
  • a graph in the drawing illustrates the result of the erosion test by water jet of the test materials A-1 and A-4 compared with a test piece of cast aluminum bronze conventionally used as propeller material. From this graph it is seen that the cast steel of this invention possesses excellent erosion resistance. Further, the cast steel of this invention is excellent in weldability. Therefore the joining, by welding, of for example 2 to pieces after the separate casting thereof is also possible.
  • an annealing is performed at 630-700 C. so that residual stress after welding may be relieved and so that suitable hardness for the workings may be obtained. After necessary workings, said material is again austenized and slowly cooled to obtain mechanical properties required.
  • the intermediate annealing at 630-700 C. can be performed, if necessary, prior to welding as well as in the casting in a singlebody mold.
  • a method of making a marine propeller of cast steel consisting of not more than 0.25 percent carbon not more than 1 percent silicon, not more than 3 percent manganese, from 5-20 percent of chromium, from 1-8 percent cobalt, from 0.5-7 percent of at least one element of the group consisting of molybdenum and tungsten, up to 8 percent Ni, up to 4 percent copper, and the remainder iron, comprising the steps of casting the propeller in separate sections, welding the separate sections together to form the propeller and then heating the welded cast propeller to a temperature between 800 to 1 ,000 C. and slowly cooling the casting at a rate of not more than 1 C. per minute.
  • a method, as set forth in claim 2, comprising the further step of aging the welded casting at a temperature of 450-600 C. to increase its strength subsequent to the slow cooling step.

Abstract

A method of making a high strength, high toughness cast steel marine propeller comprised of not more than 0.25 percent of carbon, not more than 1 percent of silicon, not more than 3 percent of manganese, from 5-20 percent of chromium, from 1-8 percent of cobalt, and from 0.5-7 percent of one or both of molybdenum and tungsten, and the remainder consisting of iron. In addition, the cast steel may contain up to 8 percent of nickel and up to 4 percent of copper, depending on the conditions. The method comprises casting the propeller into individual sections, welding said sections together, heating to a temperature of 800* to 1,000* C. and air cooling. The propeller can be aged by heating to a temperature between 450* and 700* C. If desired, the individual cast sections can be annealed prior to welding.

Description

United States Patent [151 3,66 1,658
Oda et al. [451 May 9, 1972 54] HIGH-STRENGTH AND HIGH- 3,340,048 9/1967 Floreen ..148/142 x TOUGHNESS CAST STEEL FOR 3,378,367 4/1968 Friis et a1. 148/37 X PROPELLERS AND METHOD FOR FOREIGN PATENTS OR APPLICATIONS MAKING PROPELLERS OF SAID CAST STEEL Inventors: Teishiro Oda; Makoto Nakamura; Masato Zama, all of Nagasaki-shi, Japan Mitsubishi Jukogyo Kabushiki Kaisha, Tokyo, Japan Filed: Oct. 8, 1969 Appl. No.: 864,898
Assignee:
Related US. Application Data Division of Ser. No. 643,679, June 5, 1967, abandoned.
75/123, 126, 128; 164/122; 29/504, 463, 156.8 B, 156.8 l-l, 156.8 P
References Cited UNITED STATES PATENTS 5/1966 Hammond ..75/128 R 796,733 6/1958 Great Britain ..75/128 Primary E\'aminerCharles N. Lovell v Attorney-McGlew and Toren, John J. McGlew and Alfred E. Page [57] ABSTRACT A method of making a high strength, high toughness cast steel marine propeller comprised of not more than 0.25 percent of carbon, not more than 1 percent of silicon, not more than 3 percent of manganese, from 5-20 percent of chromium, from l-8 percent of cobalt, and from 0.5-7 percent of one or both of molybdenum and tungsten, and the remainder consisting of iron. in addition, the cast steel may contain up to 8 percent of nickel and up to 4 percent of copper, depending on the conditions. The method comprises casting the propeller into individual sections, welding said sections together, heating to a temperature of 800 to l,000 C. and air cooling. The propeller can be aged by heating to a temperature between 450 and 700 C. If desired, the individual cast sections can be annealed prior to welding.
3 Claims, No Drawings CROSS REFERENCE OF RELATED APPLICATION This application is a division of copending application, Ser. No. 643,679, filed June 5, 1967, now abandoned.
SUMMARY OF THE INVENTION As ships increase in size, the propellers of ships become also larger and heavier; the weight increase of propellers requires larger amount of materials, causing an increase in the material cost and the power loss for driving propellers. Aluminum bronze has generally been used as the propeller material, but the shortage of copper resources all over the world in recent years is a serious factor which increases the material cost of marine propellers.
In order to reduce the material cost of propellers against such cost increasing tendency, it is necessary either to provide cheaper material to take the place of expensive copper alloys or to introduce materials stronger than conventional ones in order to reduce the propeller weight by making propeller blades lighter and thinner in section according to the increase of allowable stress of the used material; and the latter measure is especially desirable, because it makes possible to reduce not only the material cost but also the power loss, thus enhancing the propeller efficiency.
For the materials cheaper than copper alloys, an iron-base material, i.e., cast steel, may be considered. However, cast steel has been less frequently used as the propeller material, since its corrosion resistance against sea water as one of the requirements for propeller material is far inferior to copper alloys. Another reason why cast steel has not been widely used as a propeller material is that its mechanical properties have not been necessarily excellent as compared with conventional copper alloys.
This invention is to provide an inexpensive high-strength and high-toughness cast steel especially suitable for the marine propeller material possessing a good combination of strength, hardness, ductility and toughness and weldability. This cast steel is expected to be put into service under the condition of electric (cathodic) protection to prevent it from being corroded by sea-water. In that condition, the high hardness ensures a good erosion resistance.
It is one of the most essential features of this invention to obtain satisfactory mechanical properties even at an extremely low cooling velocity, which is usually found not only after the casting of a large-sized casting such as a propeller but also after the austenizing treatment thereof performed again after the casting.
The cast steel of this invention is characterized by containing less than 0.25 percent carbon, less than 1.0 percent silicon, less than 3.0 percent manganese, 5 to 20 percent chromium, l to 8 percent cobalt, one or both of molybdenum and tungsten from 0.5 to 7 percent, the rest consisting of iron and other impurities. Further the cast steel of this invention is characterized by less than 8 percent nickel and less than 4 percent copper, besides the above-mentioned constituents, may be added independently or in combination. The method of making propellers of cast steel of the composition set forth above comprises the steps of after casting the propeller slowly cooling it at a rate of not more than 1" C. per minute, reheating the casting to between 800 and l,000 C. for improving its strength, ductility and toughness, cooling the casting, and then aging it at 450-700 C. In making the casting it may be cast as a single unit or in individual sections; where individual sections are cast, the method of fonning the propeller includes the steps of welding the individual sections, heat treating the welded casting at 800-l,000 C. and then slowly cooling the casting at a rate of not more than 1 C. per minute. Further, whether the casting is formed as a single unit or from individual sections, the method includes the step of annealing at 630700 C.
And the cast steel of this invention is for the most part facecentered cubic austenite matrix at sufficiently high temperatures, and when it is cooled from the above condition to room temperature, most of the matrix changes to body-centered cubic ferrite or martensite, and yields precipitates of intermetallic compounds mainly consisting of the intermetallic compound of moldybdenum or tungsten, when the body-centered cubic lattic matrix is again heated to a temperature between 450 and 700 C. The purpose for precipitating the intermetallic compounds of molybdenum or tungsten is that, if the cast steel is reinforced by these intermetallic compounds, ductility and toughness of this cast steel can be maintained up to higher strength than those of-conventional cast steels reinforced by carbides.
There are many steels which have a similar composition to the cast steel of this invention and take advantage of the precipitation of intermetallic compound in the matrix of bodycentered cubic lattice, which are classified into so-called maraging steel or ferrite steel of precipitation hardening type. Each of these steels is hot forged or rolled to destroy the cast structure and is then rapidly cooled from the austenizing temperature, being further aged for use. They are not used like the cast steel of this invention which is used in the merely cast condition and, in some extreme cases, used under the condition when the cooling velocity is 01 C. per minute, because it has been understood according to the knowledge up to date that the excellent mechanical properties of maraging steel has been presumanly derived from the fine structure obtained by forging and rolling or by subsequent heat-treatment,'althou'gh it may be affected by characteristic of these intermetallic compounds.
As we have found that the above-mentioned characteristics of the intermetallic compound can be obtained in cast steel under a certain condition even if its structure is not necessarily considered fine, this invention is designed to make the most of this fact; accordingly, the cast steel of this invention is entirely different in the essence from others although it has a chemical composition similar to some of conventional materials.
The composition of the cast steel of this invention is determined by the reasons explained as follows:
Chromium: The lower limit of its content is 5 percent, because if the chromium content is lower, the corrosion resistance is poor and not proper for use in sea water even when the cathodic protection against corrosion is applied. Further, if the chromium content exceeds 20 percent, the ferrite which does not disappear at high temperature, i.e., 8-ferrite, increases in its ratio to make the steel brittle, or the Ms-point is lowered to lose the strength of the steel because of the consequent increase of retained austenite. The upper limit of chromium content is thus determined to be 20 percent.
Cobalt: The lower limit of cobalt is determined to be 1 percent, because it desirably prevents the formation of 8-ferrite and promotes the precipitation hardening by the mutual action with molybdenum. However, excessive addition of cobalt makes this steel less economical because of its high price, thus the upper limit of cobalt content has been determined to be 8 percent.
Molybdenum and tungsten are required to be added to this steel in the amount of at least 0.5 percent, because the cast steel of this invention takes advantage of the precipitation hardening by molybdenum and tungsten; the contents of more than 7 percent of molybdenum or tungsten make the steel less economical because of the cost of the two metals and lower ductility and toughness of the steel although it increases the strength. Considering these effects, the lower and upper limits of the content of the two metals are determined to be 0.5 and 7 percent, respectively.
Nickel content of less than 8 percent is established for the reason that, while the content of chromium, cobalt, melybdenum, etc., in the cast steel of this invention may be changed in accordance with the applied purpose, an austenite-forming element or nickel is added for adjustment so long as its addition does not make the steel much less economical when the suppressing of S-ferrite formation is necessary to prevent the reduction of ductility and toughness.
Copper of less than 4 percent is added considering that in the cast steel of this invention copper does not have markedly unfavorable influence on its mechanical propertiesbut has rather a favorable effect on the corrosion resistance. However, it is expected in the cast steel of this invention that the corrosion by sea water is prevented by means of cathodic protection, and so the addition of copper is not necessarily required.
Carbon content is limited to less than 0.25 percent; it is desirable from the viewpoint of the mechanical property and the weldability of the cast steel of this invention that the carbon content is as little as possible; however, too low a content of carbon makes melting difficult and the steel less economical, since high quality raw material becomes necessary. Considering the above-mentioned factors, the content limit of carbon is set in the range where the mechanical property and weldability of this cast steel are not markedly impaired. Silicon and manganese are necessary for deoxidation and their contents are permitted in accordance with common knowledge for the steels of this type. The content of manganese is somewhat higher than that of silicon, because of our consideration that manganese can substitute for nickel as an austenite-forming element.
The cast steel of this invention contains common impurities such as phosphorus and sulphur which inevitably enter intothe metal on melting; it is however, desirable to remove those impurities as much as possible so long as these impurities can be removed without any marked increase in cost.
The cast steel of this invention of which-the composition is defined for the above-mentioned reasons exhibits tensile strength from 60 to or more than 120 kg/mm, sufficiently high ductility and toughness in the as-cast condition if it is cooled at a sufficiently slow rate after casting. If the cooling rate is sufficiently high, the ductility and toughness decreases considerably. However, in this case, these propertiescan be improved by heating it to an appropriate temperature-above 900 C and then cooling it slowly. Even the material which has been cooled gradually at a sufiiciently slow cooling velocity can further improve its ductility and toughness after it is reheated. Further, if such material cooled sufficiently slowly as this is heated again in the temperature range from 450 to 700 C., e.g., 450 to 600 C., for an adequate period, precipiration hardening takes place increasing the strength, particularly the yield strength. And also, if possible, the strength, ductility, and toughness are further improved by heating the material to the range from about 950 to l,050 C. after casting, subsequent rapid cooling, and then aging it at 450 to 700 C.
Among the stresses occurring in marine propellers the bending stress is dominant; consequently the cast steel of this invention may be used more effectively as propeller material if the surface property is improved by taking advantage of the above-mentioned property of this material in such a manner that the surface is rapidly heated and rapidly cooled by such a method as high-frequency induction heating and then aged.
As explained so far, the cast steel of this invention exhibits excellent properties as the material for a marine propeller.
The following is an embodiment of the cast steel of this invention. Table 1 shows typical examples of the compositions of cast steels of this invention. Each of samples was melted in a kg and a 500 kg high-frequency melting furnace and also in a 3-ton electric-arc melting furnace, and was cast into a sand mold. The cooling velocity after casting was controlled in a heat-treating furnace. Table 2 indicates mechanical properties as well as heat-treatment conditions of the materials whose compositions are listed in Table 1.
TABLE 1. G]lEMICAL COMPOSITION 01* TESTED MATERIALS (IN WEIGHT PERCENT) Symbols of Melting sample C Si Mn Cr Co Mi Mo W 13* Cu furnace *Amount of addition on steel making; not the actual content in the alloy. A=30 kg. high-frequency melting furnace.
B =500-kg. higlrfrequency melting furnace.
C =3000-kg. electric-arc melting furnace.
TABLE 2.-MECIIANICAL PROPERTIES OF TEST MATERIALS aged at 550 C. for 5 hrs.
Roac- Nunihor 0.2 proof Tensile Elontion of Impact of test stress, strength, gation, area, strength. pieces Heat-treatment kg./mm.= kg./mm. percent percent kg.n1./cn1. A-l Slowly cooled at 0.5 C./min. after casting 62.1 117.2 14. 0 50. 2 6 0 Slowly cooled at 10 C./mln. after casting 72. 7 106.0 3. 8 .J. 7 l- 1 3 Slowlg cooled at 05 C./mln. alter casting, and aged at 500 C. for 10 hrs. alter slow 06. 2 132.9 12. 3 -15. 7 3'5 coo ng. 4 Slowly cooled at 0.5 C./min. alter casting, at 950 C. for 1 hr. after slow cooling, oil 97. 3 128. 2 12.0 50. 6 4. 6
quenched, and aged at 500 C. for 10 hrs. Slowly cooled at 0.5 C./n1in. alter casting 66. 5 110.0 19. 6 56. T 6. w y oled at 10 C./mi n. after casting 3, 10 5 2 g e, 2 1. 7 51338111; cooled at 05 C./min. after casting, and aged at 500 C. for 10 hrs. after slow 03. 4 126. 7 13. 4 52. 1 5. '1
ng. 4 Slowly cooled at 0.5 C./min. alter casting, at 950 C. for 1 hr. after slow cooling, 94.0 127.4 14.2 53. 2 6. 1
oil quenched, and aged at 500 C. for 10 hrs. Slowly cooled 0.6 C./min. alter casting 80, 3 125. 0 10. 7 41. 4 2 Slowly cooled 0.5 O./min. after casting 65, 2 118, 7 13. 6 50.6 l 4 Slowly cooled 0.5 C./rnin. after caSting 2 1 121. 4 12. 3 48. 2 5. 8 Slowly cooled 0.5 O./min. after casting. 63. 3 116.1 14. 0 51. 4 5- 3 Slowly cooled 0.5 C./min. alter casting. 62.1 119. 3 12. 7 40. J 6. 8 S lowly cooled 0.5 C./min. alter casting 64. 2 111. 3 10. 4 45. 6 l wly cooled at 0.1 C./min. after casting s 0 118.7 13.6 45.11 3. 0 Reheated at 050 C. for 2 hrs. after casting and cooling, and cooled C m 89. 4 117. 4 11.0 30. 0 5. 3 lteheatcd at 850 C. for 2 hrs. after casting and cooling, and cooled at 05 C./min 06. 4 120. 8 14. 0 -1 0 503131221 {alt/650 C. for 2 hrs. after casting and cooling, at 900 C. for 2 hrs. and cooled 06.1 124. 2 12. 8 30. 6 3. 8
z min. 1\l..... Sofluucd at 650 C. for 4 hrs. after casting and cooling, at 850 C. for 4 hrs., and 00.1 114.2 11.6 36.2 3.
cooled at 0.1 (L/min. l w y cooled at 5 (L/nriu. nfter casting, and aged at; 550 C. for 5 hrs 104.4 114. 0 6. 3 1 3.. blowly ('O01ttlill.5 (u/1111.ll-fllol f'ilstillg,at 850 C. for 5 1118., cooled at 05 C./miu., 103. 7 108.1 10. 2 51. 3 3
and aged at 550 for 5 hrs. hlowly cooled at 5 (1 ./min. alter casting, softened at 650 C. for 4 hrs., at 850 C. for 104.0 111.4 15.2 67.1
5 hrs, slowly cooled at 0.1 (X/mhr, and aged at 550 C. for 5 hrs. a- Slowly c d at 07mm. alter casting, air-cooled after at 1,000 c. for 2 hrs., and 114. a 121. 7 20.0 58. 5 1.8
wgotcl Charpyimpact test.
From Table 2 it is clear that the cast steel of this invention has excellent mechanical properties as casting material for propellers.
Further a graph in the drawing illustrates the result of the erosion test by water jet of the test materials A-1 and A-4 compared with a test piece of cast aluminum bronze conventionally used as propeller material. From this graph it is seen that the cast steel of this invention possesses excellent erosion resistance. Further, the cast steel of this invention is excellent in weldability. Therefore the joining, by welding, of for example 2 to pieces after the separate casting thereof is also possible. In this case, an annealing is performed at 630-700 C. so that residual stress after welding may be relieved and so that suitable hardness for the workings may be obtained. After necessary workings, said material is again austenized and slowly cooled to obtain mechanical properties required. The intermediate annealing at 630-700 C. can be performed, if necessary, prior to welding as well as in the casting in a singlebody mold.
What is claimed is:
1. A method of making a marine propeller of cast steel consisting of not more than 0.25 percent carbon not more than 1 percent silicon, not more than 3 percent manganese, from 5-20 percent of chromium, from 1-8 percent cobalt, from 0.5-7 percent of at least one element of the group consisting of molybdenum and tungsten, up to 8 percent Ni, up to 4 percent copper, and the remainder iron, comprising the steps of casting the propeller in separate sections, welding the separate sections together to form the propeller and then heating the welded cast propeller to a temperature between 800 to 1 ,000 C. and slowly cooling the casting at a rate of not more than 1 C. per minute.
2. A method as set forth in claim 1, wherein the individual sections are annealed at a temperature of 630-700 C. prior to the welding step.
3. A method, as set forth in claim 2, comprising the further step of aging the welded casting at a temperature of 450-600 C. to increase its strength subsequent to the slow cooling step.
* t l k

Claims (2)

  1. 2. A method as set forth in claim 1, wherein the individual sections are annealed at a temperature of 630*-700* C. prior to the welding step.
  2. 3. A method, as set forth in claim 2, comprising the further step of aging the welded casting at a temperature of 450*-600* C. to increase its strength subsequent to the slow cooling step.
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Cited By (13)

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Publication number Priority date Publication date Assignee Title
US3794445A (en) * 1969-10-31 1974-02-26 Hitachi Ltd Water turbine runner
US3915756A (en) * 1970-10-13 1975-10-28 Mitsubishi Heavy Ind Ltd Process of manufacturing cast steel marine propellers
US3982907A (en) * 1972-03-30 1976-09-28 Nippon Piston Ring Co., Ltd. Heat and wear resistant sintered alloy
US4087593A (en) * 1976-03-26 1978-05-02 Dana Corporation Drive shaft assembly and method
US4090813A (en) * 1975-05-14 1978-05-23 Hitachi, Ltd. High-efficiency turbo-machine impellers
US4204887A (en) * 1975-04-04 1980-05-27 The Foundation: The Research Institute Of Electric And Magnetic Alloys High damping capacity alloy
US4204888A (en) * 1975-05-19 1980-05-27 The Foundation: The Research Institute Of Electric And Magnetic Alloys High damping capacity alloy
US5310431A (en) * 1992-10-07 1994-05-10 Robert F. Buck Creep resistant, precipitation-dispersion-strengthened, martensitic stainless steel and method thereof
US6427759B1 (en) * 2000-06-01 2002-08-06 Brunswick Corporation Investment cast stainless steel marine propeller
US20040154706A1 (en) * 2003-02-07 2004-08-12 Buck Robert F. Fine-grained martensitic stainless steel and method thereof
US20040154707A1 (en) * 2003-02-07 2004-08-12 Buck Robert F. Fine-grained martensitic stainless steel and method thereof
US20060081309A1 (en) * 2003-04-08 2006-04-20 Gainsmart Group Limited Ultra-high strength weathering steel and method for making same
US20090008154A1 (en) * 2007-07-02 2009-01-08 Baker Hughes Incorporated Earth Boring Drill Bits Made From A Low-Carbon, High-Molybdenum Alloy

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GB796733A (en) * 1955-07-09 1958-06-18 Birmingham Small Arms Co Ltd Improvements in or relating to alloy steels
US3251683A (en) * 1962-01-16 1966-05-17 Allegheny Ludlum Steel Martensitic steel
US3340048A (en) * 1964-03-31 1967-09-05 Int Nickel Co Cold-worked stainless steel
US3378367A (en) * 1959-06-24 1968-04-16 Bofors Ab Weldable, corrosion-resisting steel

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB796733A (en) * 1955-07-09 1958-06-18 Birmingham Small Arms Co Ltd Improvements in or relating to alloy steels
US3378367A (en) * 1959-06-24 1968-04-16 Bofors Ab Weldable, corrosion-resisting steel
US3251683A (en) * 1962-01-16 1966-05-17 Allegheny Ludlum Steel Martensitic steel
US3340048A (en) * 1964-03-31 1967-09-05 Int Nickel Co Cold-worked stainless steel

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3794445A (en) * 1969-10-31 1974-02-26 Hitachi Ltd Water turbine runner
US3915756A (en) * 1970-10-13 1975-10-28 Mitsubishi Heavy Ind Ltd Process of manufacturing cast steel marine propellers
US3982907A (en) * 1972-03-30 1976-09-28 Nippon Piston Ring Co., Ltd. Heat and wear resistant sintered alloy
US4204887A (en) * 1975-04-04 1980-05-27 The Foundation: The Research Institute Of Electric And Magnetic Alloys High damping capacity alloy
US4090813A (en) * 1975-05-14 1978-05-23 Hitachi, Ltd. High-efficiency turbo-machine impellers
US4204888A (en) * 1975-05-19 1980-05-27 The Foundation: The Research Institute Of Electric And Magnetic Alloys High damping capacity alloy
US4087593A (en) * 1976-03-26 1978-05-02 Dana Corporation Drive shaft assembly and method
US5310431A (en) * 1992-10-07 1994-05-10 Robert F. Buck Creep resistant, precipitation-dispersion-strengthened, martensitic stainless steel and method thereof
US6427759B1 (en) * 2000-06-01 2002-08-06 Brunswick Corporation Investment cast stainless steel marine propeller
US20040154706A1 (en) * 2003-02-07 2004-08-12 Buck Robert F. Fine-grained martensitic stainless steel and method thereof
US20040154707A1 (en) * 2003-02-07 2004-08-12 Buck Robert F. Fine-grained martensitic stainless steel and method thereof
US6890393B2 (en) 2003-02-07 2005-05-10 Advanced Steel Technology, Llc Fine-grained martensitic stainless steel and method thereof
US6899773B2 (en) 2003-02-07 2005-05-31 Advanced Steel Technology, Llc Fine-grained martensitic stainless steel and method thereof
US20060081309A1 (en) * 2003-04-08 2006-04-20 Gainsmart Group Limited Ultra-high strength weathering steel and method for making same
US20090008154A1 (en) * 2007-07-02 2009-01-08 Baker Hughes Incorporated Earth Boring Drill Bits Made From A Low-Carbon, High-Molybdenum Alloy
US7905301B2 (en) * 2007-07-02 2011-03-15 Baker Hughes Incorporated Earth boring drill bits made from a low-carbon, high-molybdenum alloy

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