US3407865A - Method of coating metal mould walls - Google Patents
Method of coating metal mould walls Download PDFInfo
- Publication number
- US3407865A US3407865A US608239A US60823966A US3407865A US 3407865 A US3407865 A US 3407865A US 608239 A US608239 A US 608239A US 60823966 A US60823966 A US 60823966A US 3407865 A US3407865 A US 3407865A
- Authority
- US
- United States
- Prior art keywords
- mould
- metal
- walls
- gel
- carbon
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229910052751 metal Inorganic materials 0.000 title description 37
- 239000002184 metal Substances 0.000 title description 37
- 238000000034 method Methods 0.000 title description 21
- 239000011248 coating agent Substances 0.000 title description 10
- 238000000576 coating method Methods 0.000 title description 10
- 239000000499 gel Substances 0.000 description 25
- 239000000203 mixture Substances 0.000 description 24
- 239000000126 substance Substances 0.000 description 18
- 239000002904 solvent Substances 0.000 description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 13
- 229910052799 carbon Inorganic materials 0.000 description 13
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 12
- 239000007788 liquid Substances 0.000 description 12
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 10
- 229910052782 aluminium Inorganic materials 0.000 description 9
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 8
- 239000012298 atmosphere Substances 0.000 description 8
- 229910000831 Steel Inorganic materials 0.000 description 7
- 239000003349 gelling agent Substances 0.000 description 7
- 239000003350 kerosene Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000010959 steel Substances 0.000 description 7
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- KJCVRFUGPWSIIH-UHFFFAOYSA-N alpha-naphthol Natural products C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 6
- 239000004411 aluminium Substances 0.000 description 6
- 125000002837 carbocyclic group Chemical group 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 229910052759 nickel Inorganic materials 0.000 description 6
- 230000009972 noncorrosive effect Effects 0.000 description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 241000779819 Syncarpia glomulifera Species 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- -1 carbocyclic hydrocarbons Chemical class 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000001739 pinus spp. Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 235000007586 terpenes Nutrition 0.000 description 4
- 229940036248 turpentine Drugs 0.000 description 4
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 3
- 229950011260 betanaphthol Drugs 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 150000002314 glycerols Chemical class 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
- 230000000630 rising effect Effects 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 150000003505 terpenes Chemical class 0.000 description 3
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004859 Copal Substances 0.000 description 2
- 241000782205 Guibourtia conjugata Species 0.000 description 2
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 2
- 230000001464 adherent effect Effects 0.000 description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 description 2
- 159000000013 aluminium salts Chemical class 0.000 description 2
- 229910000329 aluminium sulfate Inorganic materials 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 229910052901 montmorillonite Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 230000001603 reducing effect Effects 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- 235000015096 spirit Nutrition 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- 229910001208 Crucible steel Inorganic materials 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- IXYBFZWIFLLCHQ-UHFFFAOYSA-N anthracene-9,10-dione;benzene-1,4-diol Chemical compound OC1=CC=C(O)C=C1.C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 IXYBFZWIFLLCHQ-UHFFFAOYSA-N 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 150000001717 carbocyclic compounds Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 description 1
- KDEZIUOWTXJEJK-UHFFFAOYSA-N heptacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC6=CC7=CC=CC=C7C=C6C=C5C=C4C=C3C=C21 KDEZIUOWTXJEJK-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- SLIUAWYAILUBJU-UHFFFAOYSA-N pentacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C21 SLIUAWYAILUBJU-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C3/00—Selection of compositions for coating the surfaces of moulds, cores, or patterns
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D7/00—Casting ingots, e.g. from ferrous metals
- B22D7/06—Ingot moulds or their manufacture
Definitions
- ABSTRACT OF THE DISCLOSURE A method is provided for applying a coating to metal mould walls and for simultaneously generating a nonoxidizing non-corrosive atmosphere within the mould.
- a small quantity of an ignitable gel composition is placed near the bottom of the mould and is ignited to deposit carbon on the walls of the mould and to generate the desired atmosphere.
- the gel comprises (1) certain carbocyclic compounds, (2) an inflammable liquid solvent, and (3) a gelling agent for the solvent.
- This invention relates to the production of ingots by the method in which molten metal is poured into metal moulds and is particularly concerned with the production of ingots of steel or of slabs or billets of copper, nickel or alloys of either of these.
- the invention is depicted schematically in the annexed drawing showing an ingot mould 1 containing the three-component gel composition 2 as a discrete mass therein.
- mould dressings or mould additives which reduce oxidation of the molten metal by their fluxing or reducing action and thus help to prevent the above defects.
- slags with a melting point considerably lower than that of the metal being cast, which form a molten fiuxing layer on the rising surface of cast metal
- mould dressing including those base on tar, pitch or heavy oil compositions.
- a method for the production of ingots of steel or slabs or billets of copper, nickel or alloys of either which comprises pouring the said molten metal into a metal mould, characterized in that there is placed in the mould a mixture of (1) a carbocyclic chemical substance which contains carbon, hydrogen and optionally also oxygen and/or nitrogen and which will on burning cause a deposit of carbon particles on the walls of the mould. the said particles being adherent to the said walls by reason of the adhesive action of a portion of the said substance or of a combustion product of said substance which deposits on the walls of the mould by sublimation or condensation, or which exists as a coating on.
- the carbon particles (2) an inflammable liquid and (3) a gelling agent in a quantity sufficient to render the mixture of said constituents into gel form, the said constituents in vapour form, and the gaseous products of combustion thereof, being non-oxidising and non-corrosive, and igniting the gel to cause it to burn and establish a said deposit prior to or simultaneously with the pouring of the said molten metal into the mould.
- the invention further includes, as new compositions of matter the gel compositions as aforesaid.
- the substance 1) may be a single organic chemical compound or mixture of such compounds.
- the selected carbocyclic substance should preferably not be deliquescent or hygroscopic since such substances have a tendency to introduce water vapour into the mould. It is generally found preferable to employ an aromatic compound with a high proportion of carbon in the molecule.
- a wide variety of compounds are suitable for use in carrying out the method of the invention. These include carbocyclic hydrocarbons such as naphthalene, phenanthrene, anthracene, biphenylene, naphthacene, rubrene, pentacene, heptacene, pyrene, perylene and acenaphthene.
- carbocyclic hydrocarbons such as naphthalene, phenanthrene, anthracene, biphenylene, naphthacene, rubrene, pentacene, heptacene, pyrene, perylene and acenaphthene.
- Other suitable substances are phenolic compounds (e.g. resorcinol, hydroquinone, alpha and beta-naphthol, anthraquinone quinol), esters of carbocyclic acids (e.g.
- pentaerythritol and glycerol esters of resins such as ester gum
- terpene compounds e.g. camphor, borneol, pinene or abietic acid
- certain natural or synthetic resins containing carbocyclic groups eg. phenolfor-maldehyde, co pal, terpene resins and alkyd resins
- Nitrogenous compounds may also be used, e.g. a-napthylamine and the aminoanthraquinones. Halogen-containing substances, aromatic acids and anhydrides are not preferred substances since they tend to cause corrosion.
- a particularly useful substance is a mixture of mononuclear and polynuclear aromatic alkyl hydrocarbons of the generalised structure R-Y for the lower molecular weight members of the mixture, and
- Y is an alkyl residue of up to 8 carbon atoms and R represents a mononuclear or polynuclear aromatic residue (e.g. phenyl, naphthyl and anthracyl).
- R represents a mononuclear or polynuclear aromatic residue (e.g. phenyl, naphthyl and anthracyl).
- a said mixture having ingredients ranging in molecular weight from about 180 to about 3000 and an average molecular weight of about 315, and having a net carbon content of about by weight, is commercially available (Reichold Chemicals, Inc., USA.) under the name Petrosyn C-2.
- An alogous mixtures, obtained by a high temperature Friedel- Crafts reaction, can also be employed.
- the second ingredient, the inflammable liquid may be any such but it is preferable to avoid the use of solvents which contain elements such as halogen or sulphur since these may tend to be corrosive. From the standpoints of cheapness and availability the common inflammable solvents such a solvent naphtha, mineral spirits, turpentine, white spirit and isopropyl alcohol are preferred. Other inflammable solvents such as toluene may be used or mixtures of any of the named solvents may be used. Basically it is only necessary that the liquid should be capable of ready ignition and, when burning, should ignite the said organic carbocyclic substance.
- Any gelling agent which will gel in the liquid used may be employed but it is preferred to select such as will leave no, or very little residue, which might contaminate the cast metal.
- Metal soaps, especially aluminium soaps are very suitable, e.g.:
- Aluminium stearate gels in solvent naphtha and kerosene.
- Aluminium naphthenate gels in white spirit, kerosene, turpentine and isopropyl alcohol.
- Aluminium octoate gels in white spirit, kerosene and turpentine.
- Aluminium salt of 2-ethyl hexoic acid gels in kerosene and other liquid hydrocarbons.
- alkyl ammonium montmorillonite gels in aromatic hydrocarbons and alcohols.
- the gel additives of the present invention may be employed as such but it is usually convenient to employ them in combustible containers, e.g. of cellulose nitrate film or of paper coated with a plastic or wax layer.
- combustible containers e.g. of cellulose nitrate film or of paper coated with a plastic or wax layer.
- Suitable containers are cardboard containers of the general character employed for packing pills and tablets in the pharmaceutical industry. It is of course important that the container should burn away to leave little or no residue which might contaminate the cast metal.
- the follOWing are examples of gel additives for use in the method of the invention. Percentages given are by weight.
- Example II Naphthalene 45 Kerosene 45 Aluminium napthenate
- Example III Naphthalene 40 Turpentine 55 Aluminium naphthenate 5
- Example IV Naphthalene Petrosyn C2 8 Kerosene 71 Aluminium octoate 3 Aluminium salt of 2-ethyl hexoic acid 3
- Example V Petrosyn C2 14 Solvent naphtha Kerosene 2 Aluminium stearate 4 Recommended additions are as follows: for ingots up to 500 lbs. 2-4 oz. per ton; for ingots of 500 lbs. to 5 tons, 4-10 02. per ton.
- the required quantity of the gel composition is placed in the bottom of the metal ingot mould and ignited. It is immaterial whether the mould is cold or warm at this time.
- the ignition may be effected before the molten metal is poured into the mould so that the mould, when the metal is tapped, already has the required carbon deposit, and this method of procedure is generally preferable.
- the ignition of the gel composition may, in an alternative procedure, be effected by the molten metal itself in the pouring operation.
- the gel composition burns the mould is filled with its vapours and/or the vapours of its decomposition products and an adherent carbon deposit is formed on the walls.
- the disadvantages peculiar to the previously known dressings are avoided, i.e. there is no possibility of inclusions in the cast steel deriving from the additive and there is no slag of any sort remaining on the surface of the cast metal. There is little or no fume problem.
- the simplicity of application compared to normal methods of applying mould dressing is a distinct advantage; thus there is no equipment needed to apply the product, thus avoiding capital cost and maintenance, and there is a reduction in labour costs.
- the surface quality of the ingot obtained is much less dependent on human factors.
- the coating applied to the mould surface by the method of this invention also functions as a mould release agent and it preserves the surface of the mould thus prolonging its active life.
- said material being selected from the group consisting of polynuclear hydrocarbons, resorcinol, hydroquinone, alpha-naphthol, beta-naphthol, anthraquinone, quinol, pentaerythritol, glycerol esters of resins, terpenes, phenolformaldehyde resins, copal, alphenaphthylamine and aminoanthraquinones, (2) an inflammable liquid solvent, and (3) a gelling agent for said inflammable liquid solvent in a quantity sufiicient to render said composition into gel form, and igniting the said gel composition to cause it to deposit carbon on the walls of the mould and generate in the mould a non-oxidising non-corrosive atmosphere, said gel composition being placed in the mould in a discrete mass other than a mould coating.
- a method for applying a coating to metal mould walls which comprises igniting near the bottom of said mould a quantity of an ignitable gel composition comprising three ingredients, (1) a material in an amount effective upon being burned in the mould to generate a non-oxidising non-corrosive atmosphere in the mould and a protective carbon deposit on the walls of the mould, said material being selected from the group consisting of polynuclear hydrocarbons, resorcinol, hydroquinone, alpha-naphthol, beta-naphthol, anthraquinone, quinol, pentaerythritol, glycerol esters of resins, terpenes, phenolformaldehyde resins, copal, alpha-naphthylamine and aminoanthraquinones, (2) an inflammable liquid solvent, and (3) a geling agent for said inflammable liquid solvent in a quantity sufficient to render said composition into gel form, to thereby deposit carbon on the walls of the mould and generate
- gelling agent is selected from the class consisting of aluminum stearate, aluminum naphthenate, aluminum octoate and aluminum 2-ethy1 hexoate and alkyl ammonium montmorillonite.
- composition is ignited by pouring said molten metal into said mould.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
- Continuous Casting (AREA)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4459664A GB1114258A (en) | 1964-11-06 | 1964-11-06 | Production of ingots |
US473816A US3322518A (en) | 1964-11-06 | 1965-07-21 | Production of ingots |
FR36911A FR1451906A (fr) | 1965-07-21 | 1965-11-02 | Perfectionnements apportés à la production de lingots de métaux et alliages |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4459664A GB1114258A (en) | 1964-11-06 | 1964-11-06 | Production of ingots |
Publications (1)
Publication Number | Publication Date |
---|---|
US3407865A true US3407865A (en) | 1968-10-29 |
Family
ID=10434008
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US608239A Expired - Lifetime US3407865A (en) | 1964-11-06 | 1966-10-26 | Method of coating metal mould walls |
Country Status (7)
Country | Link |
---|---|
US (1) | US3407865A (es) |
AT (1) | AT260443B (es) |
BE (1) | BE671670A (es) |
BR (1) | BR6574467D0 (es) |
DE (1) | DE1297817B (es) |
ES (1) | ES319174A1 (es) |
SE (1) | SE302828B (es) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3978908A (en) * | 1975-01-06 | 1976-09-07 | Research Corporation | Method of die casting metals |
US7030066B1 (en) | 2001-11-12 | 2006-04-18 | Charles Piskoti | Wetting composition for high temperature metal surfaces, and method of making the same |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DD229278A3 (de) * | 1983-12-23 | 1985-10-30 | Grunhain Elektromotorenwerk | Druckgussverfahren fuer leichtmetalle und deren legierungen |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2050375A (en) * | 1933-10-18 | 1936-08-11 | American Smelting Refining | Casting copper and copper alloys |
US2245651A (en) * | 1940-09-11 | 1941-06-17 | Linde Air Prod Co | Mold coating |
US2885360A (en) * | 1951-09-08 | 1959-05-05 | Minerals & Chemicals Corp Of A | Clay bodied organic liquids and a process for the preparation thereof |
US2901361A (en) * | 1956-09-06 | 1959-08-25 | Allied Asphalt & Mineral Corp | Mold release agent |
US2923041A (en) * | 1956-06-18 | 1960-02-02 | Nalco Chemical Co | Mold release agents for use in die casting |
GB847723A (en) * | 1958-05-29 | 1960-09-14 | Nat Res Dev | Improvements in or relating to parting agent compositions |
GB954723A (en) * | 1962-04-25 | 1964-04-08 | Foseco Int | A dressing for moulds used in the production of metal castings and ingots |
GB986422A (en) * | 1961-05-02 | 1965-03-17 | Foseco Int | Production of cast iron castings |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE641021C (de) * | 1935-06-02 | 1937-01-19 | Alexander Reichenberger | Glaeserspuelvorrichtung |
FR1241642A (fr) * | 1958-11-29 | 1960-09-16 | Noirs pour moules et noyaux de fonderie |
-
0
- BE BE671670D patent/BE671670A/xx unknown
-
1965
- 1965-10-28 AT AT978065A patent/AT260443B/de active
- 1965-10-29 BR BR174467/65A patent/BR6574467D0/pt unknown
- 1965-11-02 ES ES0319174A patent/ES319174A1/es not_active Expired
- 1965-11-02 SE SE14149/65A patent/SE302828B/xx unknown
- 1965-11-02 DE DEF47579A patent/DE1297817B/de active Pending
-
1966
- 1966-10-26 US US608239A patent/US3407865A/en not_active Expired - Lifetime
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2050375A (en) * | 1933-10-18 | 1936-08-11 | American Smelting Refining | Casting copper and copper alloys |
US2245651A (en) * | 1940-09-11 | 1941-06-17 | Linde Air Prod Co | Mold coating |
US2885360A (en) * | 1951-09-08 | 1959-05-05 | Minerals & Chemicals Corp Of A | Clay bodied organic liquids and a process for the preparation thereof |
US2923041A (en) * | 1956-06-18 | 1960-02-02 | Nalco Chemical Co | Mold release agents for use in die casting |
US2901361A (en) * | 1956-09-06 | 1959-08-25 | Allied Asphalt & Mineral Corp | Mold release agent |
GB847723A (en) * | 1958-05-29 | 1960-09-14 | Nat Res Dev | Improvements in or relating to parting agent compositions |
GB986422A (en) * | 1961-05-02 | 1965-03-17 | Foseco Int | Production of cast iron castings |
GB954723A (en) * | 1962-04-25 | 1964-04-08 | Foseco Int | A dressing for moulds used in the production of metal castings and ingots |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3978908A (en) * | 1975-01-06 | 1976-09-07 | Research Corporation | Method of die casting metals |
US7030066B1 (en) | 2001-11-12 | 2006-04-18 | Charles Piskoti | Wetting composition for high temperature metal surfaces, and method of making the same |
Also Published As
Publication number | Publication date |
---|---|
ES319174A1 (es) | 1966-04-16 |
BE671670A (es) | |
BR6574467D0 (pt) | 1973-02-15 |
AT260443B (de) | 1968-03-11 |
SE302828B (es) | 1968-08-05 |
DE1297817B (de) | 1969-06-19 |
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