US3108340A - Preparation of foundry cores - Google Patents
Preparation of foundry cores Download PDFInfo
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- US3108340A US3108340A US720179A US72017958A US3108340A US 3108340 A US3108340 A US 3108340A US 720179 A US720179 A US 720179A US 72017958 A US72017958 A US 72017958A US 3108340 A US3108340 A US 3108340A
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- urea
- casting
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- 238000002360 preparation method Methods 0.000 title description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 75
- 239000004576 sand Substances 0.000 claims description 66
- 239000000203 mixture Substances 0.000 claims description 49
- 238000000034 method Methods 0.000 claims description 26
- 238000005266 casting Methods 0.000 claims description 24
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 19
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 15
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 claims description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 7
- 239000004202 carbamide Substances 0.000 claims description 7
- 238000007493 shaping process Methods 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- 239000007789 gas Substances 0.000 description 34
- 229920005989 resin Polymers 0.000 description 26
- 239000011347 resin Substances 0.000 description 26
- 239000011230 binding agent Substances 0.000 description 20
- 229910052751 metal Inorganic materials 0.000 description 18
- 239000002184 metal Substances 0.000 description 18
- 239000002253 acid Substances 0.000 description 14
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 11
- 238000005058 metal casting Methods 0.000 description 8
- 150000002739 metals Chemical class 0.000 description 6
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical group O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 6
- 230000000717 retained effect Effects 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 235000013339 cereals Nutrition 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000004115 Sodium Silicate Substances 0.000 description 4
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 4
- -1 non-ferrous metals Chemical class 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 4
- 229910052911 sodium silicate Inorganic materials 0.000 description 4
- 229910001369 Brass Inorganic materials 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000010951 brass Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 238000007528 sand casting Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C1/00—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
- B22C1/16—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents
- B22C1/162—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents use of a gaseous treating agent for hardening the binder
Definitions
- This invention contributes to the foundry art and has particular reference to the preparation and provision of sand cores (and molds) useful for the casting of metals and other materials wherein said structures are desired to be produced with accurately controlled dimensional tolerances. More particularly, the present invention has reference to a new and useful technique for hardening cores and molds produced from silica sand mixes containing urea-formaldehyde resins as binders. The invention also relates to an improved method for casting metals, particularly non-ferrous metals, in molds fabricated in accordance with the present invention.
- CO process perrnits cores and molds to be made with a mixture of sand and an aqueous solution of sodium (or other alkali metal) silicate and hardened in very short order by passing carbon dioxide gas through the wet composition after it has been fabricated into a desired shape.
- the gas combines chemd lhdfidd Fatentecl @ct.
- urea-formaldehyde bonded sand compositions that are capable of being fabricated into excellent quality foundry molds and cores having high strength and excellent characteristics and features, excellent dimensional characteristics and significant and substantial freedom from generation of gas during the metal casting process.
- Yet a further object of the invention is to facilitate the casting of thin wall structures, especially with non-ferrous metals, by virtue of cores (and molds) possibilitated by practice of the present invention.
- the solidification or hardening usually occurs in an almost instantaneous manner, after which the core (or mold) may be removed from the box or other container in which it has been hardened and used for the desired metal casting purpose. It may be advantageous in certain instances to flush the hardened core with air or other inert gas to dispose of the excess acid gas which may remain therein. This tends to avoid problems of odor or toxicity prior to further handling of the fabricated structure. While cores or molds hardened in the indicated manner can be used directly for casting after the gassing, operation, they may optionally be baked, if desired, in the conventional manner to further increase their tensile strength. While such baking is not an absolute necessity for the realization of satisfactory results, it oftentimes is found to be a beneficial expedient. In any event, even when the gassed structures are baked, the time that is required for baking is generally found to be decreased by at least a third in comparison to the conventional requirements for baking when structures that are not prepared in accordance with the invention are being made.
- inorganic acid gases While a variety of inorganic acid gases may be utilized in the practice of the present invention, it is generally preferable to use such gases as sulfur dioxide (S elemental chlorine (Cl hydrogen chloride (HCl), hydro gen bromide (HBr), boron trichloride (BCl boron trifiuoride (BF;,) and the like in the practice of the invention.
- sulfur dioxide S elemental chlorine (Cl hydrogen chloride (HCl), hydro gen bromide (HBr), boron trichloride (BCl boron trifiuoride (BF;,) and the like in the practice of the invention.
- the usual conventional urea-formaldehyde resins may be employed as binders for the sand in the practice of the present invention.
- Such resins may contain from about 1.5 to 2.5 (preferably about 1.8 to 2.0) moles of formaldehyde to each mole of urea therein.
- the resins employed are condensed in the conventional manner with an alkaline catalyst (NaOH) until they have attained a water-soluble condition.
- NaOH alkaline catalyst
- the urea-formaldehyde resins are discussed by Dietert, supra, at page 95, and by Heine and Rosenthal, supra, at page 156. They are also defined at pages 908-910 of Organic Chemistry, by Fieser and Fiescr, D. C. Heath and Co., Boston (1944).
- compositions of the inven- 2 tion are customary for about 3 percent by weight or so of moisture to be present in the resulting mixture.
- a typical mixing procedure for formulating the compositions of the inven- 2 tion is as follows, using a conventional Baker-Perkins muller for the compounding:
- any ordinary sand or other refractory material may be employed in the practice of the invention.
- the sand or its equivalent that is employed has a fineness in accordance with the values proposed by the American Found-rymans Society (APS) that is in the numerical range between about 25 and 180.
- APS American Found-rymans Society
- Such sands for example, as the types which are known as Berkeley Float sand, Juniata sand, Lake sand, Muskegon Bank sand, Vassar sand, Wedron sand, Gratiot Bank sand and the like are quite suitable. It is frequently desirable in the practice of the present invention to use clean sand, although an unwashed sand may be employed.
- sand having an AFS fineness number from about 50 to 125.
- Very frequently sands that have an AFS fineness number less than 100 may be preferable for many foundry core and mold making operations.
- the screen analysis of a typical suitable sand for foundry core use is included in the following tabulation, using Gratiot Bank sand (AFS 65) for the illustration:
- Boric acid may arso be employed to improve the physical properties of the structures as well as to reduce the dwell time of the structures after gassing, i.e., the interval after gassing during which the core or other structure becomes fully hardened.
- acrylamide polymers such as polyacrylamide, may be utilized to improve the separation of the hardened structure from the container in which it is fabricated as well as to minimize the stickiness of the sand composition and render it easier to handle.
- the resin-containing sand mixture prior to the gassing, may be fabricated to the desired shape in any suitable manner.
- the mixtures may be applied directly to the forming surfaces for the mold or core by manual or mechanical ramming, or by pneumatic spraying or distributing apparatus, or by otherwise pressing the material into the shaping space or cavity provided therefor.
- the required form or shape of core or mold may be produced using a pattern, core box or equivalent means.
- core boxes or the like may be provided with apertures or passageways to permit how of the acid gas into the said mixture.
- holes or passageways for gas flow may also be provided within the fabricated mass of resin containing sand in order to facilitate distribution of the acid gas therethrough.
- the proper quantity of gas and length of time for gassing can ordinarily be gaged from results obtained with a standard compression sample having a diameter of about two inches and a length equal to the diameter prepared from sand containing about 2 percent of the urea-formaldehyde binder.
- a standard compression sample having a diameter of about two inches and a length equal to the diameter prepared from sand containing about 2 percent of the urea-formaldehyde binder.
- Example 1 A series of sand mixtures of washed Gratiot Bank sand was thoroughly mixed with an aqueous solution of urea-formaldehyde resin containing about 50 percent solids.
- the resin had a formaldehyde to urea mole ratio of about 1.8:1.
- Each of the mixtures also contained about one percent sulfur and /2 percent KBF
- the resin-containing mixtures were fabricated into standard core forms of about two inches in length by two inches in diameter which were cured by passing sulfur dioxide gas through them under about 20 p.s.i.g. until hardened. For purposes of comparison, some of the cores were baked after the gassing operation by placing them in an oven for 20 minutes at 325 F.
- cores were prepared according to the CO process using 4 percent Na SiO as a binder and CO tion similar to those set forth in the foregoing were found to be well adapted for use in the successful casting of magnesium according to conventional techniques and to provide excellent results in the finished castings.
- the castings obtained were precisely formed and had excellent- 1y smooth surface finishes, due to the substantial freedom from blowing of the bonded sand structures.
- the collapsibility and shakeout characteristics of the core for-ms prepared according to the invention were found to be excellent.
- Suitable ferrous castings can be similarly prepared.
- Example 3 The following resin-containing sand composition was intimately mix-ed, formed into cores, and gassed for 3 minutes with BCl under 20 psi. g.
- the hardness H so 15 is measured on the smooth side of the core with a Dietert No. 673 Dry Hardness Tester. In this test, the instru- Example 4 ment is pressed down on the specimen. The maximum hardness reading on a hard surface would be units.
- C Percent Compression
- T Tensile
- H Hardness
- Cores and molds prepared in accordance with the invenin Example 3 were prepared excepting to add increasing proportions of diethylene glycol to sequential samples and to gas the fabricated cores with S as in Example 1. The results were as follows:
- composition T H T H 0 (blank)... 48 72 119 65 73 85 250 93 72 83 238 92 3.... 68 80 242 92
- use of the boric acid in the compositions decreased the dwe.l time from at least 240 seconds for the blank to 210 seconds for 1 percent H 50 60 seconds for 2 percent H 80 and 70 seconds for 3 percent H 30
- Such reductions in dwell time permits efficient handling of large size cores that would otherwise be extremely difficult, if not totally impossible, to fabricate.
- the method of casting metals which comprises mixing sand with a minor proportion of between about 0.25 and 10 percent by weight, based on the weight of the dry sand in the resulting composition, of a resin binder consisting essentially of a water-soluble synthetic urea-formaldehyde resin in which the mole ratio of formaldehyde to urea is from about 1.5 to 25:1, respectively; forming a metal retaining structure of the resulting sand composition; hardening said structure by passing therethrough an acid gas selected from the group consisting of inorganic halogen acid gases of halogens of atomic number from 9 to 35 and sulfur dioxide gas; and casting the metal in the resulting mold.
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- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
Description
United States Patent 3,108,349 PREPARATEQN F FGUNDRY QURES Adolph T. Peters, Midlmd, and Robert G. La Valley,
Saginaw, Mich, assignors to The Dow Chemical (Zornpany, Midland, Mich, a corporan'ion of Delaware Filed Mar. 10, N53, Ser. No. 72h,l7 9 Claims. (Cl. 22-193) This invention contributes to the foundry art and has particular reference to the preparation and provision of sand cores (and molds) useful for the casting of metals and other materials wherein said structures are desired to be produced with accurately controlled dimensional tolerances. More particularly, the present invention has reference to a new and useful technique for hardening cores and molds produced from silica sand mixes containing urea-formaldehyde resins as binders. The invention also relates to an improved method for casting metals, particularly non-ferrous metals, in molds fabricated in accordance with the present invention.
Synthetic urea-formaldehyde resins are well known binder materials for foundry sands. They have been employed for this purpose, particularly when it is desired to fabricate cores, as well as certain mold structures, having good dimensional tolerances. In the usual practice, especially when cores and molds for sand casting of nonferrous metals are being made, there is incorporated'in the sand a binder of the urea-formaldehyde resin, a cereal additament of the conventional variety and water. The usual cereal binders that are used and the purposes of their utilization are explained by H. W. Dietert at pages 101403 of his book entitled Foundry Core Practice, 2nd Ed, published by the American Foundrymens Society (1950). They are also discussed at page 156 of Principles of Metal Casting, by R. W. Heine and P. C. Rosenthal, McGraw-Hill Book Co., Inc. 355). In addition to the resin binder and cereal, small quantities of various inhibitor additives, depending upon the particular metal being cast may also be employed in the compositions. Thus, a small amount of clay sand (bentonite) may be added to develop greater green strength. Along with these, a core oil, such as a paraffin or mineral oil, may be incorporated to aid in reducing stickiness of the sand in the green state. The refractory mixture is then baked at temperatures up to 400 F after having been fabricated into the desired shape for periods of time up to two hours or so in order to develop the requisite hardness and strength needed for the casting operation.
While the normal urea-formaldehyde/cereal bonded cores and molds are extensively employed, there are certain disadvantages attendant their utilization. For example, such compositions frequently generate excessive gas during the metal casting operation. in addition, it is a frequent experience that metal-retaining structures fabricated from such compositions are not readily shaken or removed from the casting after solidification of the metal therein or the reagent. A further disadvantage which is frequently encountered is that many cores are so shaped as to require the utilization of expensive dryer accessories to support the core during the baking operation.
There has in recent years been developed an improved method for the utilization of aqueous solutions of sodium silicate as a binder in sand compositions suitable for fabrication of foundry molds and cores. This method, which is already well known, is generally referred to as the carbon dioxide (CO process. The CO process perrnits cores and molds to be made with a mixture of sand and an aqueous solution of sodium (or other alkali metal) silicate and hardened in very short order by passing carbon dioxide gas through the wet composition after it has been fabricated into a desired shape. The gas combines chemd lhdfidd Fatentecl @ct. 29, 1963 ically with the silicate binder of the sand composition to form a silicic acid gel which cements the sand grains together and accomplishes the desired binding in periods of time that may be as short as several seconds. Sodium (and other alkali metal) silicate bonded cores and molds that have been made by the CO process can be used for metal casting very soon after the gassing of the fabricated structures. The CO process has been described at page 33 of Modern Castings for August 1956 and at page 111 of Steel for August 6, 1956.
The major disadvantage encountered in the employment of silicate bonded sand compositions in foundry molds and cores, including those that have been prepared by the CO process, is that of poor collapsibility after the metal has been poured in and solidified in the mold. This is especially true when non-ferrous metals are being cast. In contrast to organic binders, sodium (and other alkali metal) silicate does not burn out at low temperatures. To the contrary, it sinters with the sand, especially at higher temperatures, to form glasses. As a consequence, collapsibiiity and shake-out features are generally very poor and frequently inadequate in sand molds and cores bonded with sodium silicate and the like and the castings may be disadvantageously difficult to remove. In addition, sodium silicate bonded cores are also prone to generate considerable gas during the casting operation. This gives rise to undesirable blows in the casting. Besides, the sodium silicate bonded structures are quite hygroscopic and when baked, as frequently is the case, form sodium salts which have only a low refractory quality and cause thermoplasticity.
it would be an advantage and would meet a long-sought need of the foundry art to provide a method for producing cores and molds using urea-formaldehyde binders which is less time consuming and more economical than conventional practice while being capable of yielding dimensionally accurate bonded structures that have the desirable combination of properties needed for mold and core fabrication, which structures do not generate excessive gas on metal casting while having excellent collapsibility so as to be adapted to be readly shaken from the casting after solidification of the metal. Such accomplishments would be of salient benefit for present day casting requirements, especially when thin wall structures are being fabricated wherein the mentioned features, particularly dimensional accuracy, are practical desiderations of great importance.
it is the principal object of the present invention to provide urea-formaldehyde bonded sand compositions that are capable of being fabricated into excellent quality foundry molds and cores having high strength and excellent characteristics and features, excellent dimensional characteristics and significant and substantial freedom from generation of gas during the metal casting process.
It is an associated object of the present invention to provide bonded sand compositions of the indicated variety that are adapted, during the preparation of molds and cores therefrom, to be hardened in the core box so as to maintain dimensional tolerances and to have little, if any, tendency to hygroscopicity after baking. 7 Anotherobject of the invention is to provide an improved process for casting metals in and with molds and cores made of the urea-formaldehyde bonded sand compositions prepared in accordance with the present invention.
Yet a further object of the invention is to facilitate the casting of thin wall structures, especially with non-ferrous metals, by virtue of cores (and molds) possibilitated by practice of the present invention.
These and corollary objects and associated benefits and advantages may be achieved 'by practice of the present invention which comprises uniformly incorporating in a foundry sand composition for the preparation of cores and molds a minor proportion of a urea-formaldehyde resin binder; fabricating the resin-containing composition in the shape of a desired core or mold (advantageously in a core or mold box); and subsequently passing through the fabricated composition an inorganic acid gas comprised of and containing sulfur or a halogen of atomic number from 9 to 35 =(i.e., fluorine, chlorine, bromine) until the sand mixture is solidified and hardened by the action of gas. The solidification or hardening usually occurs in an almost instantaneous manner, after which the core (or mold) may be removed from the box or other container in which it has been hardened and used for the desired metal casting purpose. It may be advantageous in certain instances to flush the hardened core with air or other inert gas to dispose of the excess acid gas which may remain therein. This tends to avoid problems of odor or toxicity prior to further handling of the fabricated structure. While cores or molds hardened in the indicated manner can be used directly for casting after the gassing, operation, they may optionally be baked, if desired, in the conventional manner to further increase their tensile strength. While such baking is not an absolute necessity for the realization of satisfactory results, it oftentimes is found to be a beneficial expedient. In any event, even when the gassed structures are baked, the time that is required for baking is generally found to be decreased by at least a third in comparison to the conventional requirements for baking when structures that are not prepared in accordance with the invention are being made.
While a variety of inorganic acid gases may be utilized in the practice of the present invention, it is generally preferable to use such gases as sulfur dioxide (S elemental chlorine (Cl hydrogen chloride (HCl), hydro gen bromide (HBr), boron trichloride (BCl boron trifiuoride (BF;,) and the like in the practice of the invention.
The usual conventional urea-formaldehyde resins may be employed as binders for the sand in the practice of the present invention. Such resins, as are well known to those skilled in the art, may contain from about 1.5 to 2.5 (preferably about 1.8 to 2.0) moles of formaldehyde to each mole of urea therein. The resins employed are condensed in the conventional manner with an alkaline catalyst (NaOH) until they have attained a water-soluble condition. The urea-formaldehyde resins are discussed by Dietert, supra, at page 95, and by Heine and Rosenthal, supra, at page 156. They are also defined at pages 908-910 of Organic Chemistry, by Fieser and Fiescr, D. C. Heath and Co., Boston (1944).
Of course, as will be appreciated by those who are skilled in the art, the present invention is also capable of being successfully practiced with other resin binders in place of the urea-formaldehyde resins, such as resins of urea with other aldehydes or with the conventional and well known phenol-formaldehyde or other phenol-aldehyde resin binders for the sand.
The usual quantities of the urea-formaldehyde resin may be employed in the sand compositions as a binder. For example, amounts of the resin between about 0.25 and 8 or 10 percent by weight of the dry sand, preferably on the order of from 1 to 4 percent by weight, based on the weight of the dry sand in the composition, may ad- Vantageously be utilized in the compositions to be set and hardened by the acid gases. For economys sake it is desirable to use as small a quantity of resin maybe found adequate to secure the desired strength in the final structure. While the resin can be mixed dry with the sand, a small amount of water is generally employed along with the resin in order to obtain a wet sand mixture with the aqueous resin solution. As a matter of fact, it is customary for about 3 percent by weight or so of moisture to be present in the resulting mixture. A typical mixing procedure for formulating the compositions of the inven- 2 tion is as follows, using a conventional Baker-Perkins muller for the compounding:
A The resin can be added all dry or all liquid or partially dry and partially liquid. It is most convenient, however, to add an aqueous solution of the resin.
Sueh as inhibitors, etc., as hereinafter refercd to. This step omitted in absence of such additives.
L Such as glycols and polyglycols, as hereinafter referred-t0. This step omitted in absence of such additives.
Any ordinary sand or other refractory material may be employed in the practice of the invention. Advantageously, the sand or its equivalent that is employed has a fineness in accordance with the values proposed by the American Found-rymans Society (APS) that is in the numerical range between about 25 and 180. Such sands, for example, as the types which are known as Berkeley Float sand, Juniata sand, Lake sand, Muskegon Bank sand, Vassar sand, Wedron sand, Gratiot Bank sand and the like are quite suitable. It is frequently desirable in the practice of the present invention to use clean sand, although an unwashed sand may be employed. In many cases it may be more advantageous to utilize sand having an AFS fineness number from about 50 to 125. Very frequently sands that have an AFS fineness number less than 100 may be preferable for many foundry core and mold making operations. The screen analysis of a typical suitable sand for foundry core use is included in the following tabulation, using Gratiot Bank sand (AFS 65) for the illustration:
Percentage Icrccn toga Mesh size, U.S. by weight Mesh size, Us. by weight Standard sieve series of sand standard sieve series of sand retained on retained on screen SCIQCIl Other additives may also be incorporated with benefit in the resin-bonded sand compositions of the present invention, although satisfactory operation does not depend upon their employment. Thus oxidation-inhibitors for certain metals may be employed, such as sulfur and KBR, to prevent molten magnesium from forming oxides by reacting with moisture in the air or sand. Of course, such ingredients are not necessary for casting aluminum or brass. Likewise, glycols and Water-soluble polyglycols may be employed to increase the baked strength of the cores that are baked after gassing. Boric acid may arso be employed to improve the physical properties of the structures as well as to reduce the dwell time of the structures after gassing, i.e., the interval after gassing during which the core or other structure becomes fully hardened. In addition, acrylamide polymers, such as polyacrylamide, may be utilized to improve the separation of the hardened structure from the container in which it is fabricated as well as to minimize the stickiness of the sand composition and render it easier to handle.
The resin-containing sand mixture, prior to the gassing, may be fabricated to the desired shape in any suitable manner. Thus, the mixtures may be applied directly to the forming surfaces for the mold or core by manual or mechanical ramming, or by pneumatic spraying or distributing apparatus, or by otherwise pressing the material into the shaping space or cavity provided therefor. Advantageously, the required form or shape of core or mold may be produced using a pattern, core box or equivalent means. When core boxes or the like are utilized, they may be provided with apertures or passageways to permit how of the acid gas into the said mixture. In addition, holes or passageways for gas flow may also be provided within the fabricated mass of resin containing sand in order to facilitate distribution of the acid gas therethrough.
The quantity of the acid gas employed and the gassing time utilized depends on the resin content of the sand mixture being set and the size of the mold or core being fabricated. Suitable quantities of the gas as well as adequate gassing times can be readily determined by the skilled worker following simple and straightforward tests. Generally, too short a gassing time will cause an undesirably soft core or mold structure to be obtained. Overgassing, however, produces no deleterious effect in the fabricated structure and has no other harmful influence, other than being an uneconornical practice. The proper quantity of gas and length of time for gassing can ordinarily be gaged from results obtained with a standard compression sample having a diameter of about two inches and a length equal to the diameter prepared from sand containing about 2 percent of the urea-formaldehyde binder. When such a sample is gassed with S for about one second while passing the acid gas through the sample under a pressure of about 20 pounds per square inch gauge (p.s.i.g.), a set hardening effect is generally obtained within about one second. The gassing can be accomplished conveniently at room temperature although, if desired, lower or higher temperature conditions can also be utilized.
Further illustration of the invention is manifest in the following examples which are intended to be merely demonstrative and not limiting, wherein all parts and percentages are to be taken by weight.
Example 1 A series of sand mixtures of washed Gratiot Bank sand was thoroughly mixed with an aqueous solution of urea-formaldehyde resin containing about 50 percent solids. The resin had a formaldehyde to urea mole ratio of about 1.8:1. Each of the mixtures also contained about one percent sulfur and /2 percent KBF The resin-containing mixtures were fabricated into standard core forms of about two inches in length by two inches in diameter which were cured by passing sulfur dioxide gas through them under about 20 p.s.i.g. until hardened. For purposes of comparison, some of the cores were baked after the gassing operation by placing them in an oven for 20 minutes at 325 F. For purposes of additional comparison, cores were prepared according to the CO process using 4 percent Na SiO as a binder and CO tion similar to those set forth in the foregoing were found to be well adapted for use in the successful casting of magnesium according to conventional techniques and to provide excellent results in the finished castings. The castings obtained were precisely formed and had excellent- 1y smooth surface finishes, due to the substantial freedom from blowing of the bonded sand structures. After the casting, the collapsibility and shakeout characteristics of the core for-ms prepared according to the invention were found to be excellent. Commensurate good results are obtained when casting aluminum and brass or other nonferrous metals with the cores and molds of the invention. Suitable ferrous castings can be similarly prepared. The sulfur and KBF are not employed for aluminum, brass or iron castings. A foundry sand core fabricated from a urea-formaldehyde bonded sand com position and hardened in accordance with the present invention is illustrated in the sole FIGURE of the here-to annexed drawing.
Example 2 Baked strengths (p.s.i.) 20 mm. at 325 F.
Retained strengths (p.s.i.) 30 min. at 325 F., 60 min.
Initial strengths (p.s.1.)
at 650 F.
Example 3 The following resin-containing sand composition was intimately mix-ed, formed into cores, and gassed for 3 minutes with BCl under 20 psi. g.
Parts Gratiot Bank sand (AFS 65) 94.5 Sulfur 1 Ken, 0.5
percent aqueous solution of urea-formaldehyde resin having 1.811 aldehyde to urea mole ratio"- 4 The properties of the gassed cores were as follows:
under 15 pounds pressure for 20 seconds for curing. B k d h R (1 th e I 1 4 1 a'e strengt s etaine stren s "the results are s t orth Ill t e following tabu atio lnitialst cngths (p s,i 25min. at (D-S-U wherein Samples A and B were prepared in ac- (p.s.i.) 325 F. 325F.0 min. cordance with the invention and Sample X is the core at 650 prepared following the CO process. In the table, the compression and tensile strengths refer to results obtained 32 g+ 93 with standard tests for such properties. The hardness H so 15 is measured on the smooth side of the core with a Dietert No. 673 Dry Hardness Tester. In this test, the instru- Example 4 ment is pressed down on the specimen. The maximum hardness reading on a hard surface would be units. Several compositions basically similar to that set forth Percent Compression (C) Tensile (T) Hardness (H) Retained strength 1 AFS of resin Gassing strength, p.s.i. strength, p.s.i. Sample fineness solids in Gas timein of sand mixture seconds As gassed Baked As gassed Baked As gassed Baked C T H A" 65 1.5 S02 20 280+ 280+ 32 67 so 75 0 0 0 B a so, 30 280+ 280+ 14 as so 108 20 25 65 4 002 20 220 280+ 30 130 so 85 280+ 39 79 I In order to determine retained strength, the cores were gassed as indicated; then baked for 20 minutes at 325 F., then additionally baked for an hour at 650 F. As is obvious, lower retained strengths are a reliable measure of greater collapsibility and better shakoout characteristics.
9 Nazsiog.
Each of the cores had excellent dimensional tolerances. Cores and molds prepared in accordance with the invenin Example 3 were prepared excepting to add increasing proportions of diethylene glycol to sequential samples and to gas the fabricated cores with S as in Example 1. The results were as follows:
Initial strengths, Baked strengths, p.s.i. p.s.i. Percent 01 glycol in min. at 325 F.
composition '1 H T H Example 5 The procedure of Example 4 was duplicated with compositions containing /2 percent of the glycol and increasing resin binder contents. The results were as The procedure of Example 4 was duplicated excepting to replace the glycol additive with varying quantities of boric acid (H 30 in the several samples and to gas the cores for only 15 seconds. The results were as follows:
Initial strengths, Baked strengths, p.s.i. p.s.i. Percent of boric acid in 20 min. at 325 F.
composition T H T H 0 (blank)... 48 72 119 65 73 85 250 93 72 83 238 92 3.... 68 80 242 92 In addition, use of the boric acid in the compositions decreased the dwe.l time from at least 240 seconds for the blank to 210 seconds for 1 percent H 50 60 seconds for 2 percent H 80 and 70 seconds for 3 percent H 30 Such reductions in dwell time permits efficient handling of large size cores that would otherwise be extremely difficult, if not totally impossible, to fabricate.
What is claimed is:
1. Method for fabricating foundry cores and molds from silica sand compositions which comprises mixing said sand with between about 0.25 and 10 percent by weight, based on the weight of the dry sand in the com- 0 position, of a resin binder consisting essentially of a water-soluble synthetic urea-formaldehyde resin in which the mole ratio of formaldehyde to urea is from about 1.5 to 2.5 :1, respectively; fabricating said sand mixture into a structure suited for shaping metal by casting; and hardening said sand composition by passing therethrough an acid gas selected from the group consisting of inorganic halogen acid gases of halogens of atomic number from 9 to 35 and sulfur dioxide gas until said structure has been solidified and hardened by the action of said gas on the resin binder.
2. The method of claim 1, wherein said sand composition is mixed with between about 1 and 4 percent by weight of said resin.
3. The method of claim 1, wherein said resin sand mixture is fabricated by being shaped in a core or mold box and is hardened by passing said acid gas therethrough while said sand composition is in said box.
4. The method of claim 1, wherein said acid gas is sulfur dioxide.
5. The method of claim 1, wherein said acid gas is elemental chlorine.
6. The method of claim 1, wherein said acid gas is boron trichloride.
7. A shaped, refractory article [for metal casting as produced by the method of claim 1.
8. The method of casting metals which comprises mixing sand with a minor proportion of between about 0.25 and 10 percent by weight, based on the weight of the dry sand in the resulting composition, of a resin binder consisting essentially of a water-soluble synthetic urea-formaldehyde resin in which the mole ratio of formaldehyde to urea is from about 1.5 to 25:1, respectively; forming a metal retaining structure of the resulting sand composition; hardening said structure by passing therethrough an acid gas selected from the group consisting of inorganic halogen acid gases of halogens of atomic number from 9 to 35 and sulfur dioxide gas; and casting the metal in the resulting mold.
9. The method of claim 8, wherein said metal that is cast is a non-ferrous metal.
References Cited in the file of this patent UNlTED STATES PATENTS 1,482,357 Ellis Jan. 29, 1924 1,482,358 Ellis Jan. 29, 1924 2,229,291 Groten Jan. 21, 1941 2,422,118 Meyer June 10, 1947 2,528,934 Wiles Nov. 7, 0 2,679,490 Meiser et al May 25, 1954 2,723,253 Waudell Nov. 8, 1955 2,874,428 Bouncy Feb. 24, 1959 3,008,205 Blaies Nov. 14, 1961 FGREIGN PATENTS 710,099 Great Britain June 9, 1954 OTHER REFERENCES Foundry Trade Journal (publication), May 12, 1955.
Claims (1)
1. METHOD FOR FABRICATING FOUNDRY CORES AND MOLDS FROM SILICA SAND COMPOSITIONS WHICH COMPRISES MIXING SAID SAND WITH BETWEEN ABOUT 0.25 AND 10 PERCENT BY WEIGHT, BASED ON THE WEIGHT OF THE DRY SAND IN THE COMPOSITION, OF A RESIN BINDER CONSISTING ESSENTIALLY OF A WATER-SOLUBLE SYNTHETIC UREA-FORMALDEHYDE RESIN IN WHICH THE MOLE RATIO OF FORMALDEHYDE TO UREA IF FROM ABOUT 1.5 TO 2.5:1, RESPECTIVELY; FABRICATING SAID SAND MIXTURE INTO A STRUCTURE SUITED FOR SHAPING METAL BY CASTING; AND
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
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| US720179A US3108340A (en) | 1958-03-10 | 1958-03-10 | Preparation of foundry cores |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US720179A US3108340A (en) | 1958-03-10 | 1958-03-10 | Preparation of foundry cores |
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| US3108340A true US3108340A (en) | 1963-10-29 |
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|---|---|---|---|
| US720179A Expired - Lifetime US3108340A (en) | 1958-03-10 | 1958-03-10 | Preparation of foundry cores |
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Cited By (10)
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| US3209420A (en) * | 1963-07-05 | 1965-10-05 | Archer Daniels Midland Co | Mold and core binder for foundry use |
| US3879339A (en) * | 1971-08-16 | 1975-04-22 | Applic Prod Ind | Manufacture of solid or hollow bodies from a composition containing a granular filler |
| FR2419779A1 (en) * | 1978-03-14 | 1979-10-12 | Gerard Richard | PROCESS FOR CURING A COMPOSITION INTENDED IN PARTICULAR FOR THE MANUFACTURING OF MOLDS AND FOUNDRY CORES, AND APPARATUS FOR IMPLEMENTING THE SAID PROCESS |
| US4311627A (en) * | 1980-10-29 | 1982-01-19 | Consolidated Foundries And Mfg. Corp. | Process for curing foundry cores and molds |
| US4396526A (en) * | 1980-11-05 | 1983-08-02 | Cl Industries, Inc. | Organic hydroperoxide catalyst system |
| US4448234A (en) * | 1982-08-05 | 1984-05-15 | Cl Industries, Inc. | Method for forming sand cores and molds |
| US4518723A (en) * | 1982-08-05 | 1985-05-21 | Cl Industries, Inc. | Curable epoxy resin compositions and use in preparing formed, shaped, filled bodies |
| US4526219A (en) * | 1980-01-07 | 1985-07-02 | Ashland Oil, Inc. | Process of forming foundry cores and molds utilizing binder curable by free radical polymerization |
| US4806576A (en) * | 1982-08-05 | 1989-02-21 | Ashland Oil, Inc. | Curable epoxy resin compositions and use in preparing formed, shaped, filled bodies |
| US20100130653A1 (en) * | 2008-11-25 | 2010-05-27 | Huttenes-Albertus Chemische Werke Gmbh | Alkaline resol phenol-aldehyde resin binder compositions |
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| US1482358A (en) * | 1922-09-29 | 1924-01-29 | Ellis Carleton | Casting containing synthetic resin and process of making same |
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| US1482357A (en) * | 1922-09-26 | 1924-01-29 | Ellis Carleton | Casting synthetic resin |
| US1482358A (en) * | 1922-09-29 | 1924-01-29 | Ellis Carleton | Casting containing synthetic resin and process of making same |
| US2229291A (en) * | 1939-02-16 | 1941-01-21 | American Cyanamid Co | Molding compounds |
| US2422118A (en) * | 1942-03-13 | 1947-06-10 | Libbey Owens Ford Glass Co | Making cores for casting light metal alloys |
| US2528934A (en) * | 1949-04-29 | 1950-11-07 | Shell Dev | Adhesive composition containing a fluidized glycidyl ether and an amphoteric oxide |
| GB710099A (en) * | 1951-04-11 | 1954-06-09 | Harborough Construction Compan | Improvements in or relating to the production of moulds, cores and the like |
| US2679490A (en) * | 1951-09-06 | 1954-05-25 | Allied Chem & Dye Corp | Production of molding compositions from urea-formaldehyde and cellulose containing material |
| US2723253A (en) * | 1952-10-25 | 1955-11-08 | Sidney Haas | Thermo-settable intermediate condensation products |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3209420A (en) * | 1963-07-05 | 1965-10-05 | Archer Daniels Midland Co | Mold and core binder for foundry use |
| US3879339A (en) * | 1971-08-16 | 1975-04-22 | Applic Prod Ind | Manufacture of solid or hollow bodies from a composition containing a granular filler |
| FR2419779A1 (en) * | 1978-03-14 | 1979-10-12 | Gerard Richard | PROCESS FOR CURING A COMPOSITION INTENDED IN PARTICULAR FOR THE MANUFACTURING OF MOLDS AND FOUNDRY CORES, AND APPARATUS FOR IMPLEMENTING THE SAID PROCESS |
| US4526219A (en) * | 1980-01-07 | 1985-07-02 | Ashland Oil, Inc. | Process of forming foundry cores and molds utilizing binder curable by free radical polymerization |
| US4311627A (en) * | 1980-10-29 | 1982-01-19 | Consolidated Foundries And Mfg. Corp. | Process for curing foundry cores and molds |
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| US4396526A (en) * | 1980-11-05 | 1983-08-02 | Cl Industries, Inc. | Organic hydroperoxide catalyst system |
| US4448234A (en) * | 1982-08-05 | 1984-05-15 | Cl Industries, Inc. | Method for forming sand cores and molds |
| US4518723A (en) * | 1982-08-05 | 1985-05-21 | Cl Industries, Inc. | Curable epoxy resin compositions and use in preparing formed, shaped, filled bodies |
| US4806576A (en) * | 1982-08-05 | 1989-02-21 | Ashland Oil, Inc. | Curable epoxy resin compositions and use in preparing formed, shaped, filled bodies |
| US20100130653A1 (en) * | 2008-11-25 | 2010-05-27 | Huttenes-Albertus Chemische Werke Gmbh | Alkaline resol phenol-aldehyde resin binder compositions |
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