US2974048A - Core binder - Google Patents
Core binder Download PDFInfo
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- US2974048A US2974048A US705793A US70579357A US2974048A US 2974048 A US2974048 A US 2974048A US 705793 A US705793 A US 705793A US 70579357 A US70579357 A US 70579357A US 2974048 A US2974048 A US 2974048A
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- Prior art keywords
- core
- starch
- strength
- amylopectin
- baked
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- 239000011230 binding agent Substances 0.000 title description 25
- 229920000945 Amylopectin Polymers 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims 1
- 229920002472 Starch Polymers 0.000 description 25
- 235000019698 starch Nutrition 0.000 description 25
- 239000008107 starch Substances 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- 238000012360 testing method Methods 0.000 description 12
- 239000004576 sand Substances 0.000 description 11
- 239000006185 dispersion Substances 0.000 description 8
- 229920000881 Modified starch Polymers 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 229920000856 Amylose Polymers 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000004368 Modified starch Substances 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 235000013339 cereals Nutrition 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000010959 steel Substances 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 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 230000002452 interceptive effect Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 235000019426 modified starch Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 206010042674 Swelling Diseases 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- -1 alkali-metal orthophosphate salt Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 235000019621 digestibility Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 235000011868 grain product Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 238000005058 metal casting Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000013014 purified material Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- TWQULNDIKKJZPH-UHFFFAOYSA-K trilithium;phosphate Chemical class [Li+].[Li+].[Li+].[O-]P([O-])([O-])=O TWQULNDIKKJZPH-UHFFFAOYSA-K 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
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
- B22C1/167—Mixtures of inorganic and organic binding agents
Definitions
- the present invention relates to cores for foundry purposes. More particularly, it relates to a foundry core of high baked strength, imparted by a novel binder component.
- void :spaces in the casting are produced by incorporating cores of one sort or another in the mold.
- cores like the mold itself, are made of sand, and must include some kind of binding material to withstand the eroding action of the molten metal.
- the requirementsfor a satisfactory binder are a great deal more severe than for the external mold itself. A great deal of work has accordingly been done in the field of core binders.
- the various prior-art materials vary greatly, however, in their so-called baked strength (he, their strength after being baked, which must be suflieient -to withstand the impact and the stresses produced by themolten metal) and in their hot properties (these being the ability of the core to withstand the molten metal until solidification is Well advanced, and then .togive way thereafter so as to avoid imparting stresses in the casting).
- the present invention relatestoan improved core binder component which has the property of imparting remarkably.high'bakedstrength in foundry cores, without interfering in any way with the hot "properties thereof.
- An object of the present invention is to produce an improved foundry core.
- Another object is tolprovide an improved core binder component.
- Another object is to provide a core binder component capable of imparting high baked "strength without interfering with the hot properties *of'the core.
- Another object is to segregate the fraction of gelatinized starch capable of imparting high baked strength to foundry cores, and to remove deleterious substances therefrom.
- gelatinized amylopectin is extraordinarily effective as a component of corebinders to increase the baked strength of the resulting cores.
- gelatinized amylopectin is employed in a form substantially free from amylose and preferably substantially free from fats, proteins, fibers, and other substances commonly found in associationtherewith, and is incorporated in a foundry core in a proportion between ice 2 portion of water between about '2 andabout"6% liy weight, based on the weight of the dry mixture.
- amylopectin is preferably employed in the form .ofa
- a core sand in the desiredproportion optimally between about 0.5 and about 1.5% by weight.
- the water is preferably blended into the sand before the amylopectin.
- Amy-lopectin can also be added to other core-binder compositions, e.g., gelatinized starch, cereal (corn flour), or the like, to improve the baked strength thereof. Tne completed core mixture, when properlyblended, formed into the desired shapes, and baked, yields cores having a baked tensile strength as-high as 250 psi. or more.
- Starch appears .to be composed of two types of molestiles-a straight-chain fraction called amylose, and a branched-chain fraction called amylopectin. These two fractions are known .to .differsubstantially in physical and chemical properties, such as solubility, enzy-rne digestibility, color formation with iodine, crystallinity, viscosity in aqueous dispersion, and in other respects. The separationof the .two "fractions in their original form does not appear to have'been accomplished. In every case, it has apparently been necessary to subject the starch grantiles to at least a swelling treatment with water as a preliminary to separating the fractions. It has been reported that amylose can be extracted with hot water.
- amylose can be selectively precipitated by addition of butanol orpentanol, leaving the amylopectin in solution '(Schoch, Cereal Chem, 18 (1941)., 121; J. Am. Chem. Soc., 64 (1942), 2957).
- amylopectin thus obtained is, of course, a ,gelatinized form of the original amylopectin.
- This is the material which I have found to be particularly effective in .producing foundry cores of high baked strength without impairing the hot properties thereof.
- the dispersion can be used directly as an additive to a core mixture, preferably after distilling off the butanol or pentanol, and preferably after evaporating to produce an appropriate ratio of amylopectin and water as desired in the final core mixture.
- amylopectin dispersion can be evaporated to dryness, suitably in a spray dryeror by use of a concentrator and a drum flaker, yielding a .solid product which is readily stored, handled, and admixed with foundry sands.
- the mixture should be blended, commingled with water in the desired proportion rererably around 3 to 5% by weight) and again blended before being shaped andbaked.
- gelatinized amylopectin lies in its ability to produce a baked core, at ordinary temperature; 'i.e., when a core containing the purified material is merely allowed to stand at room temperature, it undergoes chemical and physical changes of unascertained nature which result in high baked strength Without actual baking in the manner practiced by the prior art. It is, of course, feasible to carry out a conventional type of bakingto hasten the processj but even when this is done, the temperatures and the baking 7 2,914,048 Patented Mar. 7, 196i -prior art to accomplish essentially the same result. The baking can satisfactorily be carried out, for example, at temperatures as low as around 300 to 400 F. for periods of as little as to 15 minutes.
- gelatinzed amylopectin employed as a core binder in combination with an alkali-metal phosphatemodified starch, prepared as described by Neukom in US. Patents 2,884,412 (April 28, 1959) and 2,865,762 (December 23, 1958).
- dry, ungelatinized starch is impregnated with an aqueous solution of an alkali-metal orthophosphate salt having a pH between about 4 and about 7, optimally around 6, then dried to less than about 15% water content, and heated at a temperature between about 125 and about 200 0., preferably between about 150 and about 175 C., for a period of about 1 to about 15 hours, the heating time varying inversely with the temperature.
- a modified starch is obtained thereby, having the property of dispersing rapidly in cold water to produce dispersions having a viscosity between about 1,000 and about 5,000 cp., measured in 5% aqueous dispersion at room temperature.
- modified starches are highly useful in core binders, producing cores of good hot properties.
- the baked strength of such cores (and of foundry cores in general) is materially improved by including gelatinized amylopectin in the binder, suitably in a proportion between about and about 75% by weight, based on the total binder.
- the Neukom starch phosphates are substances prepared by impregnating an ungelatinized starch with at least about 1.0% by weight, calculated as phosphorus, of at least one phosphate salt of an alkali-metal in an aqueous solution of said salt having a pH between 3.0 and about 7.5, and heating the impregnated starch in the substantial absence of unabsorbed water at a temperature between about 120 and about 175 C. for a period of about 1 to about hours.
- the preferred phosphate salts are the sodium, potassium, and lithium orthophosphates, alone or in suitable combinations with themselves and/or with orthophosphoric acid to yield a pH of the desired level in aqueous solution.
- the impregnating solution may suitably be between about 1 and about 3 molar in phosphate, and should be used in a quantity equivalent to at least about 1% by weight of phosphorus, preferably between about 3 and about 5%, based on the quantity of starch to be treated.
- the starch and solution are slurried together in the desired proportion for 5 to 10 minutes or more, then separated.
- the starch is dried at a temperature below its gelatinization point, ordinarily below about 60-80 C., depending upon the particular starch, to a moisture content around 8 to 15% or somewhat lower, and is then subjected to heat treatment as described hereinabove.
- the baked material is a phosphate-modified starch suitable for use as a core binder, and advantageously useful in combination with gelatinized amylopectin in accordance with my invention.
- Example I The following test illustrates the use of gelatinized amylopectin alone as a core binder.
- the resulting core had excellent baked strength, but relatively low hot strength.
- test cores were then prepared for measurement of the hot strength of the core mixture, measured in terms of the time required for a 1%" dia. x 2 cylindrical test core to collapse under a -lb. load at a given oven temperature.
- the test cores were The following illustrates a mixed core binder consisting of a conventional cereal-type binder plus gelatinized amylopectin.
- Hot-strength test cores baked 20 min. at 425 F., had
- Example 3 The following test illustrates the use of gelatinized amylopectin in combination with a technical-grade sodium phosphate-modified corn starch, prepared as described above, containing about 4.04% phosphorus and having a viscosity of 6310 cp. at 25 C. in 5% aqueous dispersion.
- Example 4 The core mixture of Example 3 was repeated, except that it was prepared with 3.2% of water, and the completed mixture contained 3.1% of water.
- Standard test cores had a green strength of 1.05 p.s.i., and developed high baked strength at temperatures as low as 300 F.:
- the green cores cured to a baked strength of 145 p.s.i. in 16 hours.
- Example 5 The core mixture of Example 3 was repeated, except that the proportion of phosphate-modified starch to amylopectin was :60. The completed mixture contained 5.0% water. The test cores had a green strength of 1.25 p.s.i. and a baked strength (20 min. at 425 F.) 35
- said binder includes a starch phosphate prepared by impregnating an ungelatinized starch with at least about 1.0 percent by Weight, calculated as phosphorus, of at least one phosphate salt of an alkali metal in an aqueous solution of said salt having a pH between 3.0 and about 7.5, and heating'the impregnated starch in the substantial absence of unabsorbed water at a temperature between about and about C. for a period of about 1 to about 15 hours, the length of the heating period varying inversely with the temperature.
- a foundry core from a mixture of sand, water, and cereal binder
- the improvement which comprises incorporating into said mixture as an added binder a starch fraction consisting of gelatinized amylopectin, the quantity of said starch fraction being sufiicient to produce a total proportion of gelatinized amylopectin between about 10 and about 75% by weight, based on the total binder, whereby a core of improved baked strength is obtained.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Mold Materials And Core Materials (AREA)
Description
United States Patent CORE :BINDER Jacob W. Sietsema, Northbrook, 11]., assign'or to International Minerals & Chemical Corporation, a corporationof New York No Drawing. Filed Dec. "30, 1957, .Ser. No. 705,793
4 Claims. (Cl.' 106'38.'5)
The present invention relates to cores for foundry purposes. More particularly, it relates to a foundry core of high baked strength, imparted by a novel binder component.
In the casting of metals, void :spaces in the casting are produced by incorporating cores of one sort or another in the mold. Such cores, like the mold itself, are made of sand, and must include some kind of binding material to withstand the eroding action of the molten metal. Inasmuch as the cores are largely surrounded by the molten metal, the requirementsfor a satisfactory binder are a great deal more severe than for the external mold itself. A great deal of work has accordingly been done in the field of core binders. Numerous materials have been used for this purpose in the past, including cereal products, water glass, drying oils, resins, sulfite liquor, proteinaceous materials, molasses,-olays, woodfiour, gelatinized starches, dextrinized starches, and many -other substances. In each case, it is usually found necessary to ad done or more additional binder componentsin order to produce a core approaching the desired properties. Most of the prior-art binders are capable of producing adequate green strengt i.e., sufficient strength to permit the core to be 'transferred'into a baking zone. The various prior-art materials vary greatly, however, in their so-called baked strength (he, their strength after being baked, which must be suflieient -to withstand the impact and the stresses produced by themolten metal) and in their hot properties (these being the ability of the core to withstand the molten metal until solidification is Well advanced, and then .togive way thereafter so as to avoid imparting stresses in the casting). The present invention relatestoan improved core binder component which has the property of imparting remarkably.high'bakedstrength in foundry cores, without interfering in any way with the hot "properties thereof.
An object of the present invention is to produce an improved foundry core. I
Another object is tolprovide an improved core binder component.
Another object is to provide a core binder component capable of imparting high baked "strength without interfering with the hot properties *of'the core.
Another object is to segregate the fraction of gelatinized starch capable of imparting high baked strength to foundry cores, and to remove deleterious substances therefrom.
Other objects of the invention will be apparent from the present description and claims.
I have now found that gelatinized amylopectin is extraordinarily effective as a component of corebinders to increase the baked strength of the resulting cores. For this purpose, gelatinized amylopectin is employed in a form substantially free from amylose and preferably substantially free from fats, proteins, fibers, and other substances commonly found in associationtherewith, and is incorporated in a foundry core in a proportion between ice 2 portion of water between about '2 andabout"6% liy weight, based on the weight of the dry mixture. The
amylopectin is preferably employed in the form .ofa
powder, whichis mulled or otherwise blended 'into a core sand in the desiredproportion, optimally between about 0.5 and about 1.5% by weight. The water is preferably blended into the sand before the amylopectin. Amy-lopectin can also be added to other core-binder compositions, e.g., gelatinized starch, cereal (corn flour), or the like, to improve the baked strength thereof. Tne completed core mixture, when properlyblended, formed into the desired shapes, and baked, yields cores having a baked tensile strength as-high as 250 psi. or more.
Starch appears .to be composed of two types of molestiles-a straight-chain fraction called amylose, and a branched-chain fraction called amylopectin. These two fractions are known .to .differsubstantially in physical and chemical properties, such as solubility, enzy-rne digestibility, color formation with iodine, crystallinity, viscosity in aqueous dispersion, and in other respects. The separationof the .two "fractions in their original form does not appear to have'been accomplished. In every case, it has apparently been necessary to subject the starch grantiles to at least a swelling treatment with water as a preliminary to separating the fractions. It has been reported that amylose can be extracted with hot water. from swollen corn starch granules. The most eifective-separation technique, however, starts with a starch"paste,; i.e., a dispersion prepared by boiling starch with water. From such a dispersion, amylose can be selectively precipitated by addition of butanol orpentanol, leaving the amylopectin in solution '(Schoch, Cereal Chem, 18 (1941)., 121; J. Am. Chem. Soc., 64 (1942), 2957).
The amylopectin thus obtained is, of course, a ,gelatinized form of the original amylopectin. This is the material which I have found to be particularly effective in .producing foundry cores of high baked strength without impairing the hot properties thereof. The dispersion can be used directly as an additive to a core mixture, preferably after distilling off the butanol or pentanol, and preferably after evaporating to produce an appropriate ratio of amylopectin and water as desired in the final core mixture. More conveniently, however, the amylopectin dispersion can be evaporated to dryness, suitably in a spray dryeror by use of a concentrator and a drum flaker, yielding a .solid product which is readily stored, handled, and admixed with foundry sands. When the solid ma terial is added to sand, the mixture should be blended, commingled with water in the desired proportion rererably around 3 to 5% by weight) and again blended before being shaped andbaked.
I have discovered that the effectiveness of gela'tinized amylopec'tinis far in excess of what might be expected about 0.1 and about 3% 'by weight, together with a profrom'theprioraart use of gelatinized. starch in cores. "It appears that the other constituents in gelatinized starclr' a'ct'not merely'as diluents but as active adulterants, greatly reducing the effectiveness of the amylopectin. When such materials are removed (particularly the amylose), the purified gelatinized amylopectin produces a baked strength more thantwice as great as might be expected from its behavior in the form of crude gelatinize'dstarch.
Another remarkable property of gelatinized amylopectin lies in its ability to produce a baked core, at ordinary temperature; 'i.e., when a core containing the purified material is merely allowed to stand at room temperature, it undergoes chemical and physical changes of unascertained nature which result in high baked strength Without actual baking in the manner practiced by the prior art. It is, of course, feasible to carry out a conventional type of bakingto hasten the processj but even when this is done, the temperatures and the baking 7 2,914,048 Patented Mar. 7, 196i -prior art to accomplish essentially the same result. The baking can satisfactorily be carried out, for example, at temperatures as low as around 300 to 400 F. for periods of as little as to 15 minutes.
In an especially advantageous modification of my invention, gelatinzed amylopectinis employed as a core binder in combination with an alkali-metal phosphatemodified starch, prepared as described by Neukom in US. Patents 2,884,412 (April 28, 1959) and 2,865,762 (December 23, 1958). In the Neukom method, dry, ungelatinized starch is impregnated with an aqueous solution of an alkali-metal orthophosphate salt having a pH between about 4 and about 7, optimally around 6, then dried to less than about 15% water content, and heated at a temperature between about 125 and about 200 0., preferably between about 150 and about 175 C., for a period of about 1 to about 15 hours, the heating time varying inversely with the temperature. A modified starch is obtained thereby, having the property of dispersing rapidly in cold water to produce dispersions having a viscosity between about 1,000 and about 5,000 cp., measured in 5% aqueous dispersion at room temperature. Such modified starches are highly useful in core binders, producing cores of good hot properties. The baked strength of such cores (and of foundry cores in general) is materially improved by including gelatinized amylopectin in the binder, suitably in a proportion between about and about 75% by weight, based on the total binder.
As defined in Neukom US. Patent 2,884,412, the Neukom starch phosphates are substances prepared by impregnating an ungelatinized starch with at least about 1.0% by weight, calculated as phosphorus, of at least one phosphate salt of an alkali-metal in an aqueous solution of said salt having a pH between 3.0 and about 7.5, and heating the impregnated starch in the substantial absence of unabsorbed water at a temperature between about 120 and about 175 C. for a period of about 1 to about hours.
For the preparation of phosphate-modified starches, the preferred phosphate salts are the sodium, potassium, and lithium orthophosphates, alone or in suitable combinations with themselves and/or with orthophosphoric acid to yield a pH of the desired level in aqueous solution. The impregnating solution may suitably be between about 1 and about 3 molar in phosphate, and should be used in a quantity equivalent to at least about 1% by weight of phosphorus, preferably between about 3 and about 5%, based on the quantity of starch to be treated. The starch and solution are slurried together in the desired proportion for 5 to 10 minutes or more, then separated. The starch is dried at a temperature below its gelatinization point, ordinarily below about 60-80 C., depending upon the particular starch, to a moisture content around 8 to 15% or somewhat lower, and is then subjected to heat treatment as described hereinabove. The baked material is a phosphate-modified starch suitable for use as a core binder, and advantageously useful in combination with gelatinized amylopectin in accordance with my invention.
The invention will be more clearly understood from the following operating examples. All of the tests described therein were carried out according to standard methods defined in the Foundry Sand Handbook, Sixth Edition (1952), published by the American Foundrymens Society, Chicago. All measurements are on a dry basis. In each case, the cores were prepared and tested in triplicate, and the reported results are the average of the three tests.
Example I .The following test illustrates the use of gelatinized amylopectin alone as a core binder. The resulting core had excellent baked strength, but relatively low hot strength.
No. 1 steel sand having an AFS grain fineness of 65 (AGF 65) was mulled with 5% by weight of water for 1 minute; then 1% of substantially pure, dry, gelatinized amylopectin was added, and mulling was continued for 6 minutes. The completed mixture retained 5.0% water. Standard test cores prepared therefrom had a green strength of 0.95 p.s.i. After they were baked 20 minutes at 425 F., their tensile strength at break was 265 p.s.i.
Standard cores were then prepared for measurement of the hot strength of the core mixture, measured in terms of the time required for a 1%" dia. x 2 cylindrical test core to collapse under a -lb. load at a given oven temperature. In each case, the test cores were The following illustrates a mixed core binder consisting of a conventional cereal-type binder plus gelatinized amylopectin.
No. 1 steel sand, AGF 65, was mulled with 5% water for 1 minute; then 1% of corn flour and 0.25% of dry, gelatinized, substantially pure amylopectin were added, and mulling was continued for 6 minutes. The completed mixture retained 5.0% of moisture. Standard test cores prepared therefrom had a green strength of 0.85 p.s.i. When baked at 425 F. their stength was as follows:
Baking Baked Time, Strength,
min. p.s.i.
Hot-strength test cores, baked 20 min. at 425 F., had
the following properties:
Oven Time for Temp., Collaps F. min.
Example 3 The following test illustrates the use of gelatinized amylopectin in combination with a technical-grade sodium phosphate-modified corn starch, prepared as described above, containing about 4.04% phosphorus and having a viscosity of 6310 cp. at 25 C. in 5% aqueous dispersion.
No. 1 steel sand, AGF 65, was mulled with 5% water for 1 minute; then 1% of a 50:50 mixture of the phosphate-modified starch and dry, gelatinized, substantially pure amylopectin was added, and mulling was continued for 6 minutes. The completed mixture contained 5.2% water. Standard test cores prepared therefrom had a green strength of 0.80 p.s.i. and a baked strength (20 min. at 425 F.) of 225 p.s.i. The baked cores had hot strengths as follows:
Oven Time for Temp, Collapse,
F. min.
Example 4 The core mixture of Example 3 was repeated, except that it was prepared with 3.2% of water, and the completed mixture contained 3.1% of water. Standard test cores had a green strength of 1.05 p.s.i., and developed high baked strength at temperatures as low as 300 F.:
Baked Strength, p.s.i. Baking Time, min.
300 F 400 I 450 F.
Even at room temperature, the green cores cured to a baked strength of 145 p.s.i. in 16 hours.
Example 5 The core mixture of Example 3 was repeated, except that the proportion of phosphate-modified starch to amylopectin was :60. The completed mixture contained 5.0% water. The test cores had a green strength of 1.25 p.s.i. and a baked strength (20 min. at 425 F.) 35
In accordance with the foregoing description, I claim as my invention:
1. in a method for the production of a foundry core from a mixture of sand, wat and hinder, the improvement which comprises employing as said binder a starch;
fraction consisting of gelatinized amylopectin in a proportion sufficient to produce a core of improved baked strength.
' 2. In a method for the production of a foundry core from a mixture of sand, Water, and binder, the improvement which comprises incorporating into said mixture a starch fraction consisting of gelatinized amylopectin in a proportion sufiicient to produce a core of improved baked strength.
3. The method of claim 2 wherein said binder includes a starch phosphate prepared by impregnating an ungelatinized starch with at least about 1.0 percent by Weight, calculated as phosphorus, of at least one phosphate salt of an alkali metal in an aqueous solution of said salt having a pH between 3.0 and about 7.5, and heating'the impregnated starch in the substantial absence of unabsorbed water at a temperature between about and about C. for a period of about 1 to about 15 hours, the length of the heating period varying inversely with the temperature.
4. In a method for the production of a foundry core from a mixture of sand, water, and cereal binder, the improvement which comprises incorporating into said mixture as an added binder a starch fraction consisting of gelatinized amylopectin, the quantity of said starch fraction being sufiicient to produce a total proportion of gelatinized amylopectin between about 10 and about 75% by weight, based on the total binder, whereby a core of improved baked strength is obtained.
References Cited in the file of this patent UNITED STATES PATENTS 1,938,574 Bauer Dec. 12, 1933 1,974,915 Giesecke Sept. 25, 1934 2,779,693 Pacsu et a1. Jan. 29, 1957 2,884,412 Neukorn Apr. 28, 1959 FOREIGN PATENTS 543,202 Great Britain Feb. 13, 1942 OTHER REFERENCES Foundry, February 1950, page 177.
Claims (1)
1. IN A METHOD FOR THE PRODUCTION OF A FOUNDRY CORE FROM A MIXTURE OF SAND, WATER, AND BINDER, THE IMPROVEMENT WHICH COMPRISES EMPLOYING AS SAID BINDER A STARCH FRACTION CONSISTING OF GELATINIZED AMYLOPECTIN IN A PROPORTION SUFFICIENT TO PRODUCE A CORE OF IMPROVED BAKED STRENGTH.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US705793A US2974048A (en) | 1957-12-30 | 1957-12-30 | Core binder |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US705793A US2974048A (en) | 1957-12-30 | 1957-12-30 | Core binder |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2974048A true US2974048A (en) | 1961-03-07 |
Family
ID=24834973
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US705793A Expired - Lifetime US2974048A (en) | 1957-12-30 | 1957-12-30 | Core binder |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2974048A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5320157A (en) * | 1993-01-28 | 1994-06-14 | General Motors Corporation | Expendable core for casting processes |
| US5582231A (en) * | 1995-04-28 | 1996-12-10 | General Motors Corporation | Sand mold member and method |
| US20040000739A1 (en) * | 2002-06-28 | 2004-01-01 | Sandsmart, Inc. | Composition and method of forming sand sculptures |
| EP0816299B2 (en) † | 1996-06-28 | 2006-10-18 | Südzucker Aktiengesellschaft Mannheim/Ochsenfurt | Additive for building materials on the basis of amylopectin |
| WO2011073715A1 (en) | 2009-12-18 | 2011-06-23 | Tenedora Nemak, S.A. De C.V. | Binder composition and method of forming foundry sand cores and molds |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1938574A (en) * | 1931-07-24 | 1933-12-12 | Stein Hall Mfg Co | Dextrinization of starch in cereals |
| US1974915A (en) * | 1928-12-26 | 1934-09-25 | Int Patents Dev Co | Gelatinized starch |
| GB543202A (en) * | 1940-08-27 | 1942-02-13 | John Nicolson | Improvements in and relating to the production of sand cores for foundry purposes |
| US2779693A (en) * | 1952-03-07 | 1957-01-29 | Textile Res Inst | Fractionation of starch |
| US2884412A (en) * | 1953-09-04 | 1959-04-28 | Int Minerals & Chem Corp | Phosphate-modified starches and preparation |
-
1957
- 1957-12-30 US US705793A patent/US2974048A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1974915A (en) * | 1928-12-26 | 1934-09-25 | Int Patents Dev Co | Gelatinized starch |
| US1938574A (en) * | 1931-07-24 | 1933-12-12 | Stein Hall Mfg Co | Dextrinization of starch in cereals |
| GB543202A (en) * | 1940-08-27 | 1942-02-13 | John Nicolson | Improvements in and relating to the production of sand cores for foundry purposes |
| US2779693A (en) * | 1952-03-07 | 1957-01-29 | Textile Res Inst | Fractionation of starch |
| US2884412A (en) * | 1953-09-04 | 1959-04-28 | Int Minerals & Chem Corp | Phosphate-modified starches and preparation |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5320157A (en) * | 1993-01-28 | 1994-06-14 | General Motors Corporation | Expendable core for casting processes |
| US5582231A (en) * | 1995-04-28 | 1996-12-10 | General Motors Corporation | Sand mold member and method |
| US5837373A (en) * | 1995-04-28 | 1998-11-17 | General Motors Corporation | Sand mold member and method |
| USRE36001E (en) * | 1995-04-28 | 1998-12-22 | General Motors Corporation | Sand mold member and method |
| EP0816299B2 (en) † | 1996-06-28 | 2006-10-18 | Südzucker Aktiengesellschaft Mannheim/Ochsenfurt | Additive for building materials on the basis of amylopectin |
| US20040000739A1 (en) * | 2002-06-28 | 2004-01-01 | Sandsmart, Inc. | Composition and method of forming sand sculptures |
| US6899755B2 (en) * | 2002-06-28 | 2005-05-31 | Sandsmart, Inc. | Composition and method of forming sand sculptures |
| WO2011073715A1 (en) | 2009-12-18 | 2011-06-23 | Tenedora Nemak, S.A. De C.V. | Binder composition and method of forming foundry sand cores and molds |
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