US3222315A - Process for making sand cores - Google Patents

Process for making sand cores Download PDF

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Publication number
US3222315A
US3222315A US35406A US3540660A US3222315A US 3222315 A US3222315 A US 3222315A US 35406 A US35406 A US 35406A US 3540660 A US3540660 A US 3540660A US 3222315 A US3222315 A US 3222315A
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US
United States
Prior art keywords
sand
binder
parts
core
weight
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
Application number
US35406A
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English (en)
Inventor
Sidney L Singer
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Individual
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Individual
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Filing date
Publication date
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Priority to US35406A priority Critical patent/US3222315A/en
Priority to GB11680/61A priority patent/GB985175A/en
Priority to ES0266393A priority patent/ES266393A1/es
Priority to CH622761A priority patent/CH402290A/de
Priority to LU40199D priority patent/LU40199A1/xx
Priority to BE604574A priority patent/BE604574A/fr
Priority to DK240361AA priority patent/DK105077C/da
Application granted granted Critical
Publication of US3222315A publication Critical patent/US3222315A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16Compositions 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
    • B22C1/20Compositions 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 of organic agents
    • B22C1/22Compositions 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 of organic agents of resins or rosins
    • B22C1/2233Compositions 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 of organic agents of resins or rosins obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • B22C1/224Furan polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22CFOUNDRY MOULDING
    • B22C1/00Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds
    • B22C1/16Compositions 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
    • B22C1/20Compositions 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 of organic agents
    • B22C1/22Compositions 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 of organic agents of resins or rosins
    • B22C1/2233Compositions 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 of organic agents of resins or rosins obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G16/00Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
    • C08G16/02Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
    • C08G16/025Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with heterocyclic organic compounds
    • C08G16/0256Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with heterocyclic organic compounds containing oxygen in the ring
    • C08G16/0262Furfuryl alcohol

Definitions

  • the sand is bonded together into a unitary mass by means of a binder, such as petroleum oil, pitch, clays, and like substances.
  • a binder such as petroleum oil, pitch, clays, and like substances.
  • the cores resulting from such bonding have surfaces which are not sturdy enough to withstand handling or the force of the molten metal in casting.
  • the sand for making cores or molds has also been bonded together by means of binders, such as resins, drying oils, cements, and the like.
  • the cores or molds resulting from the use of the last-mentioned binders have greater strength than those produced from the first-mentioned binders, but they have to be dried or baked in order to set or develop strength.
  • Urea formaldehyde and phenol formaldehyde resins have been used to bond sands for making sand cores or molds, but these resins are not easy to incorporate with the sand, because they are deficient in sand wettability and flow, and require heating to set or cure the resins before the core or mold may be used in casting molten metal.
  • sand cores can be produced which have the inherent properties of excellent sand wettability and storage stability extending over indefinite periods by employing a binder in the form of a liquid resin and Obtained by reacting urea, formaldehyde, and furfuryl alcohol together as the bonding medium for the sand employed in the formationof the sand core or mold. It has been further found that by the addition of a setting agent or accelerator the set of the resin or binder can be controlled to a given time schedule at normal room temperature, obviating baking or heat curing.
  • an object of the present invention is to provide a process for producing a core composed substantially of sand which possesses the property of excellent wettability and retains its stability for long periods of storage.
  • Another object of the present invention is to provide a process for producing a core composed principally of sand which is especially adapted for foundry practice and which requires no baking or heat curing.
  • a further object of the present invention is to provide a process for producing a core composed principally of sand which is simple in execution, and commercially feasible.
  • the process of the present invention comprises incorporating with sand in quantity sufficient to form a core an acidic accelerator and a liquid binder in the form of a resin and obtained by reacting together urea, formaldehyde, and furfuryl alcohol.
  • the acidic accelerator employed may be selected from the group consisting of phosphoric acid of 75% to 85% strength, sulfuric acid, hydrochloric acid, ammonium phosphate, carbamide phosphoric acid, hemi-sodium phosphate, borophosphoric acid, ammonium chloride, sodium bisulfate.
  • An acidic accelerator made by dissolving 3 parts by weight of sodium bisulfate in 7 parts by Weight of glycolic acid has been used successfully.
  • urea, formaldehyde, and furfuryl alcohol are reacted together in the mole ratio of 1-2 to 1-2 to l-4. Also, this reaction is carried out in the presence of a condensing agent, such as diethylene triamine, but it is to be understood that any other amine, alkalimetal hydroxide, ammonium hydroxide, or calcium hydroxide may be used.
  • a condensing agent such as diethylene triamine, but it is to be understood that any other amine, alkalimetal hydroxide, ammonium hydroxide, or calcium hydroxide may be used.
  • the acidic accelerator may be admixed with resin obtained by reacting urea, formaldehyde and furfuryl alcohol together or the sand may be impregnated with the acidic accelerator followed by incorporation of the aforesaid resin with the impregnated sand.
  • the latter procedure is the preferred one.
  • Example 1 60 parts by weight of formaldehyde, 60 parts by weight of urea, 65 parts by weight of furfuryl alcohol and 0.3 part by weight of diethylene triamine are heated under agitation to 150 F., and held at this temperature for 3 hours. The temperature is raised to 210 F. and distillation allowed to take place under a slight vacuum. parts of water are distilled out, condensed and removed from the system. The resultant material constitutes the binder in the form of a resin.
  • This binder is used to make a mold cavity by the following procedure: To 1000 parts of foundry sand are added 7 parts of an activator made by dissolving 3 parts of sodium bisulfate in 7 parts of glycolic acid, 70% technical grade. The mixture of sand and activator is mulled for 2 minutes in a slow speed muller. 20 parts of the binder is added and mulling continued for 3 minutes longer. The mixture is then removed from the muller, packed around a pattern and allowed to cure at room temperature. In about 25 minutes the pattern is removed from the sand without deformation of the mold. After standing for an additional 2 hours the mold is ready for use and molten metal is poured into the cavity. A sound casting is obtained.
  • Example 2 30 parts by weight of formaldehyde, 60 parts by weight of urea, 65 parts by weight of furfuryl alcohol and 0.3 parts by weight of diethylene triamine are used and the same manufacturing procedure as set forth in Example 1 is followed for the making of the binder. 55 parts of water are distilled out, condensed, and removed from the system. The binder thus made is used to make a mold cavity by the same procedure as set forth in Example 1, with good results.
  • Example 3 The binder is made with parts by weight of formaldehyde, 60 parts by weight of urea, 65 parts by weight of furfuryl alcohol and 0.3 part by weight of diethylene triamine. The same manufacturing procedure is followed as in Example 1 and 220 parts by weight of water are removed from the system as above set forth. The binder thus made is used as set forth in Example 1 with good results.
  • Example 4 60 parts by weight of formaldehyde, 60 parts by weight of urea, 30 parts by weight of furfuryl alcohol and 0.3 part by weight of diethylene triamine are used to make a binder. The same procedure is followed as in Example 1, both as to manufacture and use to make a sound casting.
  • Example 5 The same ingredients are used and the same procedure is followed as set forth in Example 1 in the manufacture of my binder except that to the material as constituted after the removal of the water, I add 55 parts by weight of furfuryl alcohol. The binder thus produced is then used to prepare a mold in accordance with the Example 6 Using the same ingredients and following the same manufacturing procedure as set forth in Example 1, after the removal of water, an additional 175 parts by weight of furfuryl alcohol are added. The material is then used to make a mold in accordance with the procedure set forth in Example 1 with good results.
  • Example 1 With the binders made in the preceding six examples the use procedure as outlined in Example 1 may be varied.
  • the activator may be reduced to as little as 3 parts by weight per 1000 parts by weight of sand.
  • the setting time may be prolonged to, say, 4 hours and the mold thus formed is ready for molten metal in about 24 hours.
  • the activator is increased to parts by weight, the time is approximately halved.
  • a viscosity of about 1 poise is preferred, but it is to be understood that a greater viscosity can be tolerated. If the resin is of a relatively high viscosity the period of time for mulling the binder or resin and the sand is extended. The higher viscosity binder or resin gives higher green strength in the sand mixtures. Therefore, where higher green strength is desired, a more viscous resin or binder is preferred.
  • the sand-binder-accelerator mixture when freshly made, is quite light in color, provided that the sand is light in color. On standing, the mixture gradually becomes darker. This change in color is a useful indicator of the degree of set and enables the operator to judge whether or not it is time to remove the pattern.
  • the core resulting from the process of this invention shows not only excellent sand wettability, but also storage stability extending over indefinite periods.
  • core as used in the description and claims is intended to cover cores for foundry molds and as cavities into which molten metals are poured.
  • the process for making a core composed principally of sand which comprises preparing a liquid resinous binder made by heating urea, aqueous formaldehyde, and furf-uryl alcohol, in the mole ratio of 1 to 2 of urea to 1 to 2 of formaldehyde, to 1 to 4 of furfuryl alcohol in the presence of a basic condensing agent, and thereafter distilling off the major amount of water, adding the binder and acidic accelerator therefor to sand in quantity suf ficient to form said core agitating the mixture to effect thorough dissemination of the binder and accelerator through the sand, packing the disseminated mass about a pattern to form a core, and allowing the core to cure without the application of any extraneous heat.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Mold Materials And Core Materials (AREA)
  • Phenolic Resins Or Amino Resins (AREA)
US35406A 1960-06-13 1960-06-13 Process for making sand cores Expired - Lifetime US3222315A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US35406A US3222315A (en) 1960-06-13 1960-06-13 Process for making sand cores
GB11680/61A GB985175A (en) 1960-06-13 1961-03-30 Amino plastic binders for the production of sand cores
ES0266393A ES266393A1 (es) 1960-06-13 1961-04-07 Un procedimiento para hacer machos de arena
CH622761A CH402290A (de) 1960-06-13 1961-05-29 Verfahren zum Herstellen von Gussformen und Kernen
LU40199D LU40199A1 (de) 1960-06-13 1961-05-30
BE604574A BE604574A (fr) 1960-06-13 1961-06-02 Procédé d'élaboration de noyaux en sable.
DK240361AA DK105077C (da) 1960-06-13 1961-06-12 Fremgangsmåde til fremstilling af en støbeform eller -kerne samt bindemiddel til anvendelse ved fremgangsmåden.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US35406A US3222315A (en) 1960-06-13 1960-06-13 Process for making sand cores

Publications (1)

Publication Number Publication Date
US3222315A true US3222315A (en) 1965-12-07

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ID=21882484

Family Applications (1)

Application Number Title Priority Date Filing Date
US35406A Expired - Lifetime US3222315A (en) 1960-06-13 1960-06-13 Process for making sand cores

Country Status (7)

Country Link
US (1) US3222315A (de)
BE (1) BE604574A (de)
CH (1) CH402290A (de)
DK (1) DK105077C (de)
ES (1) ES266393A1 (de)
GB (1) GB985175A (de)
LU (1) LU40199A1 (de)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3919127A (en) * 1972-08-25 1975-11-11 Wolff & Kaaber Polyfuran foams and a method of preparing same
US3975319A (en) * 1973-08-14 1976-08-17 Wolff & Kaaber Polyfuran foams and a method of preparing same
US3975318A (en) * 1973-08-14 1976-08-17 Wolff & Kaaber Polyfuran foams and a method of preparing same
DE2831528A1 (de) * 1978-07-18 1980-02-07 Kruglikov Verfahren zur herstellung von karbamidfuranharz
DE3020089A1 (de) * 1979-05-25 1980-11-27 Ashland Oil Inc Formmasse fuer giessereikerne und -formen und ihre verwendung
US4371648A (en) * 1980-05-12 1983-02-01 Ashland Oil, Inc. Composition containing furfuryl alcohol and use thereof in foundry binders
US5459183A (en) * 1993-05-19 1995-10-17 Schuller International, Inc. Low VOC furan resins and method of reducing VOCS in furan resins
US5534612A (en) * 1992-05-19 1996-07-09 Schuller International, Inc. Glass fiber binding compositions, process of making glass fiber binding compositions, process of binding glass fibers, and glass fiber compositions
US6077883A (en) * 1992-05-19 2000-06-20 Johns Manville International, Inc. Emulsified furan resin based glass fiber binding compositions, process of binding glass fibers, and glass fiber compositions

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2335701A (en) * 1942-01-21 1943-11-30 Ellis Foster Co Coating composition and process of making it
US2442118A (en) * 1943-07-29 1948-05-25 Rca Corp Coupling device for high-frequency apparatus
US2468056A (en) * 1944-10-24 1949-04-26 Carborundum Co Abrasive articles and method of manufacturing the same
US2510496A (en) * 1946-12-24 1950-06-06 American Cyanamid Co Furfurylated urea resins and method of preparation
US2518388A (en) * 1945-04-18 1950-08-08 American Cyanamid Co Resin adhesives and processes of producing same
US2634255A (en) * 1949-09-23 1953-04-07 American Cyanamid Co Craze-resistant adhesive having improved storage stability
US2923989A (en) * 1960-02-09 Self-lubricating shell molds
US3008205A (en) * 1958-09-19 1961-11-14 Gen Motors Corp Shell type molds and cores

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2923989A (en) * 1960-02-09 Self-lubricating shell molds
US2335701A (en) * 1942-01-21 1943-11-30 Ellis Foster Co Coating composition and process of making it
US2442118A (en) * 1943-07-29 1948-05-25 Rca Corp Coupling device for high-frequency apparatus
US2468056A (en) * 1944-10-24 1949-04-26 Carborundum Co Abrasive articles and method of manufacturing the same
US2518388A (en) * 1945-04-18 1950-08-08 American Cyanamid Co Resin adhesives and processes of producing same
US2510496A (en) * 1946-12-24 1950-06-06 American Cyanamid Co Furfurylated urea resins and method of preparation
US2634255A (en) * 1949-09-23 1953-04-07 American Cyanamid Co Craze-resistant adhesive having improved storage stability
US3008205A (en) * 1958-09-19 1961-11-14 Gen Motors Corp Shell type molds and cores

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3919127A (en) * 1972-08-25 1975-11-11 Wolff & Kaaber Polyfuran foams and a method of preparing same
US3975319A (en) * 1973-08-14 1976-08-17 Wolff & Kaaber Polyfuran foams and a method of preparing same
US3975318A (en) * 1973-08-14 1976-08-17 Wolff & Kaaber Polyfuran foams and a method of preparing same
DE2831528A1 (de) * 1978-07-18 1980-02-07 Kruglikov Verfahren zur herstellung von karbamidfuranharz
DE3020089A1 (de) * 1979-05-25 1980-11-27 Ashland Oil Inc Formmasse fuer giessereikerne und -formen und ihre verwendung
US4246167A (en) * 1979-05-25 1981-01-20 Ashland Oil, Inc. Foundry binder composition
US4371648A (en) * 1980-05-12 1983-02-01 Ashland Oil, Inc. Composition containing furfuryl alcohol and use thereof in foundry binders
US5534612A (en) * 1992-05-19 1996-07-09 Schuller International, Inc. Glass fiber binding compositions, process of making glass fiber binding compositions, process of binding glass fibers, and glass fiber compositions
US5719228A (en) * 1992-05-19 1998-02-17 Schuller International, Inc. Glass fiber binding compositions, process of making glass fiber binding compositions, process of binding glass fibers, and glass fiber compositions
US6077883A (en) * 1992-05-19 2000-06-20 Johns Manville International, Inc. Emulsified furan resin based glass fiber binding compositions, process of binding glass fibers, and glass fiber compositions
US5459183A (en) * 1993-05-19 1995-10-17 Schuller International, Inc. Low VOC furan resins and method of reducing VOCS in furan resins
US5545825A (en) * 1993-05-19 1996-08-13 Schuller International, Inc. Low VOC furan resins and method of reducing VOCs in furan resins

Also Published As

Publication number Publication date
ES266393A1 (es) 1961-09-01
CH402290A (de) 1965-11-15
GB985175A (en) 1965-03-03
LU40199A1 (de) 1961-07-31
BE604574A (fr) 1961-10-02
DK105077C (da) 1966-08-15

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