US3765876A - Method of making nodular iron castings - Google Patents
Method of making nodular iron castings Download PDFInfo
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- US3765876A US3765876A US00302762A US3765876DA US3765876A US 3765876 A US3765876 A US 3765876A US 00302762 A US00302762 A US 00302762A US 3765876D A US3765876D A US 3765876DA US 3765876 A US3765876 A US 3765876A
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- 238000005266 casting Methods 0.000 title abstract description 43
- 229910001141 Ductile iron Inorganic materials 0.000 title abstract description 16
- 238000004519 manufacturing process Methods 0.000 title description 4
- 238000000034 method Methods 0.000 claims abstract description 51
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 30
- 239000000956 alloy Substances 0.000 claims abstract description 30
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000005864 Sulphur Substances 0.000 claims abstract description 20
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910001018 Cast iron Inorganic materials 0.000 claims abstract description 10
- 229910000861 Mg alloy Inorganic materials 0.000 claims abstract description 10
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 9
- 150000002910 rare earth metals Chemical class 0.000 claims abstract description 6
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims description 18
- 229910052684 Cerium Inorganic materials 0.000 claims description 17
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 16
- 229910052791 calcium Inorganic materials 0.000 claims description 16
- 239000011575 calcium Substances 0.000 claims description 16
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 10
- 229910052710 silicon Inorganic materials 0.000 claims description 10
- 239000010703 silicon Substances 0.000 claims description 10
- 229910000676 Si alloy Inorganic materials 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 230000003750 conditioning effect Effects 0.000 claims description 7
- MKPXGEVFQSIKGE-UHFFFAOYSA-N [Mg].[Si] Chemical group [Mg].[Si] MKPXGEVFQSIKGE-UHFFFAOYSA-N 0.000 claims description 6
- 229910021346 calcium silicide Inorganic materials 0.000 claims description 5
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 4
- QCCDYNYSHILRDG-UHFFFAOYSA-K cerium(3+);trifluoride Chemical group [F-].[F-].[F-].[Ce+3] QCCDYNYSHILRDG-UHFFFAOYSA-K 0.000 claims description 4
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 4
- 229910052748 manganese Inorganic materials 0.000 claims description 4
- 239000011572 manganese Substances 0.000 claims description 4
- 229910052779 Neodymium Inorganic materials 0.000 claims description 3
- 229910000990 Ni alloy Inorganic materials 0.000 claims description 3
- 229910052788 barium Inorganic materials 0.000 claims description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 3
- ATTFYOXEMHAYAX-UHFFFAOYSA-N magnesium nickel Chemical compound [Mg].[Ni] ATTFYOXEMHAYAX-UHFFFAOYSA-N 0.000 claims description 3
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 abstract description 43
- 239000002184 metal Substances 0.000 abstract description 43
- 238000012360 testing method Methods 0.000 abstract description 25
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract description 22
- 239000011777 magnesium Substances 0.000 abstract description 22
- 229910052749 magnesium Inorganic materials 0.000 abstract description 21
- 239000000203 mixture Substances 0.000 abstract description 10
- 230000008018 melting Effects 0.000 abstract description 6
- 238000002844 melting Methods 0.000 abstract description 6
- 229910002804 graphite Inorganic materials 0.000 abstract description 5
- 239000010439 graphite Substances 0.000 abstract description 5
- 230000005496 eutectics Effects 0.000 abstract description 4
- 238000007792 addition Methods 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 150000001247 metal acetylides Chemical class 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000005997 Calcium carbide Substances 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- CLZWAWBPWVRRGI-UHFFFAOYSA-N tert-butyl 2-[2-[2-[2-[bis[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]amino]-5-bromophenoxy]ethoxy]-4-methyl-n-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]anilino]acetate Chemical compound CC1=CC=C(N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)C(OCCOC=2C(=CC=C(Br)C=2)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)=C1 CLZWAWBPWVRRGI-UHFFFAOYSA-N 0.000 description 4
- 230000001143 conditioned effect Effects 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 230000009931 harmful effect Effects 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- -1 rare earth (cerium) fluoride Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910000882 Ca alloy Inorganic materials 0.000 description 1
- 229910000636 Ce alloy Inorganic materials 0.000 description 1
- 229910000519 Ferrosilicon Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 241000212342 Sium Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 238000005087 graphitization Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000005058 metal casting Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000003245 working effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C1/00—Refining of pig-iron; Cast iron
- C21C1/10—Making spheroidal graphite cast-iron
Definitions
- ABSTRACT The method of producing a nodular cast iron casting comprising the melting of a cast iron bath of low sulphur content and near eutectic composition with a chill value of no more than eight thirty-seconds inch as measured by a standard wedge test.
- the bath is preconditioned by adding a rare earth and an alkaline earth containing alloy in an amount sufficient to increase the chill value from 50 to 150 percent and then pouring the bath into a mold having at least one reservoir and a dam skimmer gate with the reservoir containing from one-fourth to 1 4 percent by weight of a magnesium alloy.
- the last mentioned alloy is sufficient in amount to retain at least 0.01 percent magnesium in the metal from the bath which passes through the alloy so as to produce a casting containing nodular graphite.
- My invention relates to nodular iron castings and more particularly to an improved method of producing nodular graphitecast iron of high as-cast ductility and superior mechanical properties.
- Another object is to avoid the effects of structure deterioration which is common with conventionally made nodular irons.
- Another object is to produce a nodular iron casting free from carbides in the as-cast condition and having a high nodule" count and a high as-cast ductility.
- Another object is to provide a method where the extent of nodularization can be effectively adjusted to suit the casting section being produced and to avoid the occurrence of mixed and inferior graphite structures in the casting.
- FIG. 1 is a drawing showing the gating system for three test bar castings, A, B and C.
- 1, 2 and 3 are the three test bars; 4, 5 and 6 are ingates into these bars from the runner bar 7 which is connected to the dam gate 8 having the alloy 9 in its reservoir and connected to a downsprue 10.
- These test bars were cast according to the method of this invention.
- FIGS. 2A, 2B and 2C are a set of photomicrographs of the structures obtained in bars A, B, and C shown in FIG. 1 and cast without the benefit of Step No.2 of this invention. These are marked 2A, 2B and 2C.
- 2A is the structure obtained in the Bar A at a point farthest from the ingate 4. Bars B and C showed similar structures at the same points farthest away from ingates 5 and 6.
- 2B is the structure obtained in the center of Bar A in the area where the tensile bar was machined.
- 2C is the structure obtained in Bar B in the center where the tensile bar was machined. This is essentially the same structure as found in Bar C in the center.
- FIGS. 3A and. 38V are a set of photomicrographs taken from the bars of FIG. 1, but where Step No. 2 of the method of this invention was used.
- 3A represents the structure taken from the center of Bar A
- 38 is the structure taken from the center of Bar C.
- the structure from the center of Bar B was essentially the same as that shown in 3A and 3B.
- the conventional method of making nodular iron is to add any one or any combination of various wellknown nodularizing agents particularly cerium, magnesium and calcium alloys to molten metal in sufficient quantity to reduce the sulfur content to a low value and leave residual nodularizing elements in the composition to promote the formation of graphite or carbon in the nodular form.
- nodular iron contains volative nodularizing agents such as magnesium which gradually volatilizes from the metal thereby decreasing the degree of nodularization. Additionally, the graphitizing effect of silicon alloys added which is part of most procedures for making nodular iron also tends to fade with time, leading to a product containing free carbides which are nonmachinable and brittle.
- nodularizing alloys particularly those containing magnesium is accompanied by violent pyrotechnical action which is harmful from a standpoint of ecology and which because of its violence, is difficult to control quantitatively.
- One of the methods now being used is that of incorporating the graphitizing silicon alloy or the nodularizing alloy or both directly into the mold gating system. In this way, pyrotechnics are avoided and decay of structure is avoided because additions are being made at the last possible moment, that is, during the casting operation.
- the methodof my invention also proposes addition of at least part of the nodularizing alloy directly into the gating system of the mold but is an integrated process comprising a sequence of events and steps that will result in a consistent end product avoiding the difficulties presently associated with nodularizing in the mold.
- My process is best described and illustrated by some tests conducted to illustrate and highlight the difficulties associated with methods now being used by those skilled in the art.
- FIGS. 2A, 2B and 2C show the structures involved in these test bars.
- Bar A was satisfactory in every way.
- Bar C was unsatisfactory, although part of it had a suitable chemical analysis and
- Bar B was unsatisfactory although the structure in one area was every bit as good as that in Bar A.
- My invention is based on the discovery that magnesium cannot be added in a completely uniform manner in the gating system of a mold, and that the ill effects of nonuniform magnesium content can be negated by careful pre-treatment of the molten metal in the ladle prior to casting it in a mold containng magnesium alloy. This can be done in a manner that avoids pyrotechnics and fading decay during the normal useful pouring life of the metal in the mold and in a manner that insures uniformly good results in the casting.
- the first step of the method of my invention involves melting a base iron of conventional chemistry for nodular iron and of low sulphur content.
- This involves a carbon content ranging from 3.30 to 4.00, a silicon content from 1.0 to 3.0, a manganese content of 0.20 to 1.00, a phosphorous content of 0.02 to 0.10 and a sulphur content of 0.005 to 0.06 percent. Chemical contents outside of these limits may also be used for special purposes. Alloys for special effects such as nickel, molybdenum or copper may also be used.
- the important feature is that the iron with. respect to carbon and sili con should be at or near eutectic in composition, having a carbon equivalent ranging from about 4.0 to 4.6 percent.
- Step 2 where a nodulariz ation agent is added, will reduce the sulphur content to a value well below 0.02 percent, it is normal to first reduce this sulphur by other less expensive means. I prefer a sulphur content ofless than 0.025 percent and even less than 0.015 percent before Step 2 of this method is conducted.
- the method I prefer to reduce sulphur to this value is the use of calcium carbide as a clesulphurizer and a porous plug as a means of agitation of the metal. This procedure is well-known to those skilled in the art.
- the second step of the process of my invention is the critical one in that I have found that when successfully conducted, it pre-conditions the metal so that possible ineffective nodularization in the gating system of the mold is unlikely to occur. I have, in fact,-conditioned the metal in the ladle so that the process of nodularizetion in the mold is less critical and the end product is a more uniform nodular casting.
- the second step of the invention consists of adding an agent containing rare earth elements mainly cerium and alkaline earth elements, mainly calcium, to the metal in the ladle so as to change the chill value of the metal to a value related to the initial chill value of the bath. What I wish to do is increase this chill value by a definite amount.
- the first is that calcium and cerium will not increase the chill value until they have first effectively neutralized the sulphur content.
- the sulphur content has been neutralized, calcium and cerium begin to produce metastable carbides in the melt thereby increasing the chill value.
- a very effective control tool in pre-conditioning the metal for subsequent nodularization in the mold becomes available. This is an essential feature of the process of my invention.
- the original chill value of the bath as measured on a standard test wedge such asare with a one-half inch back and a 28 wedge angle is preferred at no more than eight thirty-seconds.
- higher chill values may lead to the production of stable carbides rather than metastable carbides when Step 2 is conducted by adding cerium and calcium. Stable carbides would adversely affect the structure in the final castings.
- the only way to be sure that metastable carbides are present is to start with a metal of high graphitizing value that is a low chill value and then cause this chill value to increase because of the cerium and calcium added. l actually prefer a base metal chill value of one thirty-second to four thirty-seconds inch although a value as high as eight thirty-seconds inch would still be acceptable.
- Calcium and cerium are added to the bath in Step 2 until the chill value increases by at least 50 percent but preferably by not more than 150 percent.
- the increased value would be three thirty-seconds to five thirtyseconds.
- a bath of initial chill value of four thirty-seconds inch would be changed to a chill value of eight thirtyscconds inch of higher by a successful Step 2 treatment ofthis invention.
- a typical mixture used for Step 2 of this invention would consist of 80 percent calcium silicide and percent rare earth (cerium) fluoride.
- An amount that would increase the chill value as desired would range from one-eighth to 1 1/8 percent and more usually about three-fourths percent depending on the sulphur content of the bath.
- Other combinations of calcium and cerium are also effective, but this is a matter of local preference and economics.
- the important feature of Step 2 of this invention is to introduce sufficient calcium and cerium into the melt to give a measurable increase in the chill value of the metal. When this has been done, the metal has been suitably pre-conditioned for final Step 3, which consists of complete nodularization in the gating system of the mold.
- Another rare earth which may be used is neodymium and another alkaline earth material is barium.
- Step 3 of this invention consists of casting the metal of Step 2 in a mold which contains a magnesium-silicon alloy in a suitably designed gating system.
- the metal flows over the alloy and dissolves it on its way to that part of the mold constituting the casting itself.
- the dissolved alloy results in the production ofa fully nodular structure characterized by a large number of small perfectly formed nodules in a largely ferritic matrix and with the complete absence of hard brittle carbides.
- Step 3 I prefer to use a dam gate arrangement well known to those skilled in the art, although other skimmer devices can also be used.
- This dam gate consists of a metal reservoir and a skimmer core which keeps all dirt and products of reaction from entering the mold cavity.
- the relative size of the reservoir is important in terms of the volume occupied by the magnesiumsilicon alloy. I prefer to size this reservoir so that the weight or volume of alloy used will occupy no less than 25 percent but no more than 50 percent of the volume of the reservoir. This ensures the best condition for uniform solution of this alloy during the pouring time of the casting.
- the rate of flow of metal is governed by the choke under the skimmer core and is according to normally acceptable foundry practice where the pouring rate is equal approximately to one to one and one/- fourth times the square root of the weight of metal poured.
- the alloy used may be any alloy containing magnesium and silicon and its preferred size is about one-fourth to one-eighth mesh because this size will dissolve reasonably uniformly.
- the magnesium-silicon alloy may be replaced with a magnesium-nickel alloy.
- the amount of alloy added is dependent primarily on the duration of the pouring time of the mold but will generally be so that total retained magnesium in the final metal casting is at least 0.01 percent based upon the weight of metal and usually is not more than 0.10 percent. This means that more than this be available initially and I prefer that the magnesium initially available be from 0.04 percent to 0.20 percent based upon the weight of metal.
- the total amount of silicon or nickel available initially should be from 0.10 percent to 1.0 percent. l have found that these amounts of magnesium and silicon while not too critical, give the best results under most conditions.
- I may use more than one reservoir dam gate in the gating system where the metal is poured relatively slowly and where the casting is complex and is gated at several different points.
- This selection of the exact gating system would relate basically to casting geometry as is well known to those skilled in the art.
- a multiple of dam gates may tend to give more uniform solution of the alloy which is always desirable but which has been rendered less critical by the pre-conditioning of the metal accomplished in Step 2 of the method of this invention. Without such preconditioning the solution rate and uniformity would become so critical that inferior castings could result.
- the criticality of Step 3 has been reduced to the point where it is possible to make commercially acceptable castings.
- This metal was desulphurized using 1 percent calcium carbide and agitation supplied with a porous plug and nitrogen gas. The sulphur content was reduced to 0.01 percent and the chill value of the bath was measured and found to be three thirty-seconds inch on a wedge having a one-half inch back and a 28 angle.
- the bath was then treated with an addition of fiveeighths percent of a mixture containing 80 percent 'calcium silicide and 20 percent rare earth fluorides.
- the sulphur content was further reduced to 0.005 percent and the chill value was increased to seven thirtyseconds inches.
- This pre-conditioned metal was cast into the mold where one-half percent by weight of oneeighth inch mesh, percent magnesium, 40 percent silicon alloy had been placed in the dam gate reservoir.
- the resultant test bar castings were numbered A, B and C as was the case in the experiment described in FIG. 1, and they were then tested to give the following results in Table 3.
- nondular cast iron castings comprising melting a cast iron bath of low sulphur content and near eutectic composition with a chill value of no more than eight thirty-seconds inch as measured by a standard wedge test, pre-conditioning said bath by adding a rare earth and an alkaline earth containing alloy in an amount sufficient to increase the chill value from 50 to percent and then pouring said bathinto a mold having at least one reservoir and dam skimmer gate with said reservoir containing from one-fourth to l 7 percent by weight based upon the weight of cast iron of a magnesium alloy, said last mentioned alloy being sufficient in amount to retain at least 0.01 percent magnesium based upon the weight of cast iron in the metal from said bath passing through said alloy so as to produce a casting containing nodular graphite.
- said cast iron bath has a carbon content from 3.30 to 4.00 percent, a silicon-content from 1.0 to 3.0 percent, a manganese content from 0.20 to 1.00 percent, and a phosphorous content from 0.02 to 0.10 percent, said cast iron in said bath or after said pre-conditioning step having a sulphur content from 0.005 to 0.06 percent.
- cerium is cerium fluoride and said calcium is calcium silicide.
- magnesium alloy is magnesium silicon alloy or magnesium nickel alloy.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30276272A | 1972-11-01 | 1972-11-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3765876A true US3765876A (en) | 1973-10-16 |
Family
ID=23169102
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00302762A Expired - Lifetime US3765876A (en) | 1972-11-01 | 1972-11-01 | Method of making nodular iron castings |
Country Status (19)
Country | Link |
---|---|
US (1) | US3765876A (ru) |
JP (1) | JPS5614055B2 (ru) |
AR (1) | AR195739A1 (ru) |
AU (1) | AU469766B2 (ru) |
BE (1) | BE803531A (ru) |
BR (1) | BR7306324D0 (ru) |
CA (1) | CA979221A (ru) |
DD (1) | DD108771A5 (ru) |
DE (1) | DE2342277A1 (ru) |
DK (1) | DK131004B (ru) |
FI (1) | FI54867C (ru) |
FR (1) | FR2204690B1 (ru) |
GB (1) | GB1437372A (ru) |
IT (1) | IT993721B (ru) |
NL (1) | NL7314978A (ru) |
NO (1) | NO135017C (ru) |
PL (1) | PL87816B1 (ru) |
SU (1) | SU587872A3 (ru) |
ZA (1) | ZA732522B (ru) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3870512A (en) * | 1973-03-05 | 1975-03-11 | Deere & Co | Method of producing spheroidal graphite cast iron |
US4227924A (en) * | 1978-05-18 | 1980-10-14 | Microalloying International, Inc. | Process for the production of vermicular cast iron |
US4245691A (en) * | 1977-12-02 | 1981-01-20 | Ford Motor Company | In situ furnace metal desulfurization/nodularization by high purity magnesium |
US4806157A (en) * | 1983-06-23 | 1989-02-21 | Subramanian Sundaresa V | Process for producing compacted graphite iron castings |
US4989662A (en) * | 1990-02-27 | 1991-02-05 | General Motors Corporation | Differential pressure, countergravity casting of a melt with a fugative alloyant |
US5038846A (en) * | 1990-02-27 | 1991-08-13 | General Motors Corporation | Differential pressure, countergravity casting with alloyant reaction chamber |
US5178826A (en) * | 1991-06-01 | 1993-01-12 | Foseco International Limited | Method and apparatus for the production of nodular or compacted graphite iron castings |
US5249619A (en) * | 1991-10-30 | 1993-10-05 | Mack Trucks, Inc. | Brake element and a preparation process therefor |
US20090183848A1 (en) * | 2005-12-20 | 2009-07-23 | Novacast Technologies Ab | Process for Production of Compacted Graphite Iron |
WO2011015005A1 (zh) * | 2009-08-07 | 2011-02-10 | Yang Jinde | 一种球墨铸铁行星架的铸造方法 |
CN102492891A (zh) * | 2011-12-23 | 2012-06-13 | 天津市万路科技有限公司 | 蠕化剂的生产及其应用 |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4094279A (en) * | 1976-05-07 | 1978-06-13 | Johnson Products Div. Of Sealed Power Corporation | Ductile iron roller tappet body and method for making same |
JPS5810966B2 (ja) * | 1978-02-06 | 1983-02-28 | 川崎重工業株式会社 | ダクタイル鋳鉄の製造法 |
JPS5823443B2 (ja) * | 1978-08-07 | 1983-05-16 | 川崎重工業株式会社 | ダクタイル鋳鉄の製造法 |
JPH0651410B2 (ja) * | 1983-02-25 | 1994-07-06 | セイコーエプソン株式会社 | サーマルプリンタ |
JPS6089390A (ja) * | 1983-10-24 | 1985-05-20 | Nec Corp | 印字装置 |
CH660376A5 (de) * | 1984-07-26 | 1987-04-15 | Fischer Ag Georg | Verfahren zur herstellung von gusseisen mit kugelgraphit. |
JPH01168479A (ja) * | 1987-12-25 | 1989-07-03 | H Ee L:Kk | スタンパ |
GB0614705D0 (en) * | 2006-07-25 | 2006-09-06 | Foseco Int | Improved meethod of producing ductile iron |
US8056604B2 (en) * | 2009-09-04 | 2011-11-15 | Ask Chemicals L.P. | Process for preparing a test casting and test casting prepared by the process |
CN102688993B (zh) * | 2012-06-19 | 2015-02-25 | 西峡县众德汽车部件有限公司 | Sb元素在高强度球墨铸铁瓦盖中的应用 |
JP6823512B2 (ja) | 2017-03-16 | 2021-02-03 | 本田技研工業株式会社 | 経路決定装置、車両制御装置、経路決定方法、およびプログラム |
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- 1973-04-12 ZA ZA732522A patent/ZA732522B/xx unknown
- 1973-04-30 GB GB2034573A patent/GB1437372A/en not_active Expired
- 1973-05-02 AU AU55125/73A patent/AU469766B2/en not_active Expired
- 1973-05-31 JP JP6177273A patent/JPS5614055B2/ja not_active Expired
- 1973-07-30 CA CA177,677A patent/CA979221A/en not_active Expired
- 1973-08-06 DK DK431173AA patent/DK131004B/da unknown
- 1973-08-07 NO NO3152/73A patent/NO135017C/no unknown
- 1973-08-09 IT IT27712/73A patent/IT993721B/it active
- 1973-08-13 FI FI2538/73A patent/FI54867C/fi active
- 1973-08-13 BE BE134509A patent/BE803531A/xx unknown
- 1973-08-16 BR BR6324/73A patent/BR7306324D0/pt unknown
- 1973-08-20 FR FR7330118A patent/FR2204690B1/fr not_active Expired
- 1973-08-22 DE DE19732342277 patent/DE2342277A1/de active Pending
- 1973-08-24 AR AR249750A patent/AR195739A1/es active
- 1973-08-28 PL PL1973164892A patent/PL87816B1/pl unknown
- 1973-08-30 DD DD173181A patent/DD108771A5/xx unknown
- 1973-09-28 SU SU731963902A patent/SU587872A3/ru active
- 1973-10-31 NL NL7314978A patent/NL7314978A/xx not_active Application Discontinuation
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US2542655A (en) * | 1949-09-17 | 1951-02-20 | Int Nickel Co | Gray cast iron |
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US2792300A (en) * | 1954-04-14 | 1957-05-14 | John A Livingston | Process for the production of nodular iron |
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Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3870512A (en) * | 1973-03-05 | 1975-03-11 | Deere & Co | Method of producing spheroidal graphite cast iron |
US4245691A (en) * | 1977-12-02 | 1981-01-20 | Ford Motor Company | In situ furnace metal desulfurization/nodularization by high purity magnesium |
US4227924A (en) * | 1978-05-18 | 1980-10-14 | Microalloying International, Inc. | Process for the production of vermicular cast iron |
US4806157A (en) * | 1983-06-23 | 1989-02-21 | Subramanian Sundaresa V | Process for producing compacted graphite iron castings |
US4989662A (en) * | 1990-02-27 | 1991-02-05 | General Motors Corporation | Differential pressure, countergravity casting of a melt with a fugative alloyant |
US5038846A (en) * | 1990-02-27 | 1991-08-13 | General Motors Corporation | Differential pressure, countergravity casting with alloyant reaction chamber |
US5178826A (en) * | 1991-06-01 | 1993-01-12 | Foseco International Limited | Method and apparatus for the production of nodular or compacted graphite iron castings |
US5249619A (en) * | 1991-10-30 | 1993-10-05 | Mack Trucks, Inc. | Brake element and a preparation process therefor |
US20090183848A1 (en) * | 2005-12-20 | 2009-07-23 | Novacast Technologies Ab | Process for Production of Compacted Graphite Iron |
WO2011015005A1 (zh) * | 2009-08-07 | 2011-02-10 | Yang Jinde | 一种球墨铸铁行星架的铸造方法 |
CN102492891A (zh) * | 2011-12-23 | 2012-06-13 | 天津市万路科技有限公司 | 蠕化剂的生产及其应用 |
CN102492891B (zh) * | 2011-12-23 | 2014-04-09 | 天津市万路科技有限公司 | 蠕化剂的生产及其应用 |
Also Published As
Publication number | Publication date |
---|---|
JPS5614055B2 (ru) | 1981-04-02 |
JPS4977818A (ru) | 1974-07-26 |
BR7306324D0 (pt) | 1974-10-22 |
FR2204690B1 (ru) | 1977-02-25 |
ZA732522B (en) | 1974-03-27 |
DD108771A5 (ru) | 1974-10-05 |
NL7314978A (ru) | 1974-05-03 |
IT993721B (it) | 1975-09-30 |
FI253873A (ru) | 1975-02-14 |
FI54867B (fi) | 1978-12-29 |
GB1437372A (en) | 1976-05-26 |
SU587872A3 (ru) | 1978-01-05 |
AR195739A1 (es) | 1973-10-31 |
FR2204690A1 (ru) | 1974-05-24 |
NO135017B (ru) | 1976-10-18 |
AU469766B2 (en) | 1976-02-26 |
FI54867C (fi) | 1979-04-10 |
DK131004B (da) | 1975-05-12 |
CA979221A (en) | 1975-12-09 |
NO135017C (ru) | 1977-01-26 |
BE803531A (fr) | 1973-12-03 |
AU5512573A (en) | 1974-11-07 |
DK131004C (ru) | 1975-10-13 |
DE2342277A1 (de) | 1974-05-09 |
PL87816B1 (ru) | 1976-07-31 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: MEEHANITE WORLDWIDE CORPORATION, SOUTH CAROLINA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:MEEHANITE METAL CORPORATION, A MO. CORP.;REEL/FRAME:004651/0769 Effective date: 19861212 Owner name: MEEHANITE WORLDWIDE CORPORATION, 112 CAROLINA COVE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:MEEHANITE METAL CORPORATION, A MO. CORP.;REEL/FRAME:004651/0769 Effective date: 19861212 |