US1091690A - Core compound. - Google Patents

Core compound. Download PDF

Info

Publication number
US1091690A
US1091690A US73776212A US1912737762A US1091690A US 1091690 A US1091690 A US 1091690A US 73776212 A US73776212 A US 73776212A US 1912737762 A US1912737762 A US 1912737762A US 1091690 A US1091690 A US 1091690A
Authority
US
United States
Prior art keywords
liquor
compound
core
compounds
core compound
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
US73776212A
Inventor
Hugh K Moore
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US73776212A priority Critical patent/US1091690A/en
Application granted granted Critical
Publication of US1091690A publication Critical patent/US1091690A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • B22C1/167Mixtures of inorganic and organic binding agents
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00939Uses not provided for elsewhere in C04B2111/00 for the fabrication of moulds or cores

Definitions

  • This invention has for its object to provide what is termed a core compound; that is, an adhesive or cementitious material which ma be used in connection with sand or earth or making cores such as are used in casting.
  • waste liquors comprise water, more or less sulfurous acid, various organic acids, lignone, organic sulfids or sulfonates and sugar-resembling compounds, largely pentoses. I have found that this waste liquor may be utilized in making core compounds, and thus I am able to utilize for commercial purposes what has heretofore been regarded as material substantially unfit for use.
  • this liquor can be used as a core compound, but its mode of treatment has been such that it has not been wholly eflicient in that the proportion of compound to sand or earth required to make the cores was so great that -it offered no advantages over such compounds as flour, molasses, etc.
  • I have found that I am able to greatly increase the binding or cementitious qualities of the waste liquor-by a mode of treatment which consists in evaporating at low temperatures and in vacuo the waste liquor and then adding to the resultant a relatively small quantity of sodium silicate or other equivalent compound.
  • the acids should be neutralized and this can be accomplished in any one of a variety of ways.
  • an alkaline base for the purpose of exactly neutralizing the a c1ds.
  • I may use calcium hydroxid.
  • the neutralization is se cured by causing the acid to pass through the body of the base and agitating the liquor so that all of the acid will be brought mto contact with the lime and be effectively neutralized. Care must be taken not to add too much of the base as this would cause the precipitation of the numerous organic materials contained in the liquor.
  • the amount of the alkaline base which must be used will depend upon the condition of the liquor and this of course varies in different cases due to the temperature at which the sulfite fiber may have been cooked while in the digester and to the temperature at which the digester is blown.
  • soluble silicate preferably sodium silicate, and this may be obtained on the open market at a consistency resembling molasses.
  • the compound thus the former acting as a bin inexpensive sands or earths, such for instance as what 15 known as gangway sand and secure as excellent results as though ades of sands and earths were employed in making cores, and I further find that the compound may be used in the proportion of substantially 80 to 90 parts in volume of sand to 1 part in volume of the compound, whereas, so far as I am aware, the proportion' in which the best compounds now on the market are used, is 1 part to 30 parts.
  • the core After the core has been made, it is subjected to bakin in the usual manner and is thereafter su stantially impervious to water, so that there is no danger of its absorbing moisture prior to its use in casting.
  • the baking; of'co'urse is accomplished at high tempertures to bring the cores to red heat, and, during such baking, the sodium silicate is probably decomposed, the sodium uniting with'the sulfite gases given off by the decomposition of the organic sulfites or sulfonates of the liquor.
  • the silicic acid higher given off during such decomposition is probdecomposed into silica and as steam and er between the sand and the organic solids of This is my theory of the act-ion althoughI have not fy it. I know as a that the results ably largely water, the latter evaporatin particles of the liquor. of the sodium silicate, been able as yet to veri practical matter, however, seem to justify the theory.
  • the core When being used in casting, the core retains its form during the initial setting of the molten metal, but due to the high temperature to which it is raised, the silicate and the organic salts, with which it is united or bonded, are ruptured, as it were, so as to destroy their cementitious qualities and the core may be removed as ordinarily. (This likewise is theoretical, but, as before stated,
  • a compound such as herein described is not only more efiicient than those heretofore used, but is very cheap on account of the utilization of the waste liquors.
  • the herein described core compound which consists of a' mixture of neutralized waste liquor resulting from the manufacture of sulfite fiber and a soluble silicate.
  • the herein described core compound which consists of a homogeneous mixture of neutralized evaporated waste liquor resulting from the manufacture of sulfite fiber and sodium silicate.

Description

CROSS murmur UNITED STATES PATENT OFFICE.
HUGH K. 100315, 0]? BERLIN, NEW HAMPSHIRE.
CORE COMPOUND.
Specification of Letters Yatent.
Patented Mar. 31, 1914..
lo Drawing. Application filed December 8, 1910, Serial No. 596,284. Renewed December 19, 1912. Serial To all whom it may concern:
Be it known that I, HUGH K. Moons, of Berlin, in'the .county of Coos and State of New Hampshire, have invented certain new and useful Improvements in Core Compounds, ofwhich the following is a specification.
This invention has for its object to provide what is termed a core compound; that is, an adhesive or cementitious material which ma be used in connection with sand or earth or making cores such as are used in casting.
In the manufacture of sulfite fiber, after the contents of the digester have been discharged into the blow pit and the cellulose fibers have been separated from the waste liquors, the latter have usually been discharged into rivers and streams as worthless. 'These waste liquors comprise water, more or less sulfurous acid, various organic acids, lignone, organic sulfids or sulfonates and sugar-resembling compounds, largely pentoses. I have found that this waste liquor may be utilized in making core compounds, and thus I am able to utilize for commercial purposes what has heretofore been regarded as material substantially unfit for use. It has heretofore been suggested that this liquor can be used as a core compound, but its mode of treatment has been such that it has not been wholly eflicient in that the proportion of compound to sand or earth required to make the cores was so great that -it offered no advantages over such compounds as flour, molasses, etc. I have found that I am able to greatly increase the binding or cementitious qualities of the waste liquor-by a mode of treatment which consists in evaporating at low temperatures and in vacuo the waste liquor and then adding to the resultant a relatively small quantity of sodium silicate or other equivalent compound. Of course it will be understood that, before the evaporation of the watery constituents of the liquor, the acids should be neutralized and this can be accomplished in any one of a variety of ways.
As an example of one way of practisin the process'which I have invented and o producing the improved product, I may cite the following. A small quantity of the digester liquor to be treated is first tested for the purpose of determining the presence of the free acids, and then to the liquor is earth.
added an exact quantity of an alkaline base for the purpose of exactly neutralizing the a c1ds. As the alkaline base, I may use calcium hydroxid. The neutralization is se cured by causing the acid to pass through the body of the base and agitating the liquor so that all of the acid will be brought mto contact with the lime and be effectively neutralized. Care must be taken not to add too much of the base as this would cause the precipitation of the numerous organic materials contained in the liquor. The amount of the alkaline base which must be used will depend upon the condition of the liquor and this of course varies in different cases due to the temperature at which the sulfite fiber may have been cooked while in the digester and to the temperature at which the digester is blown. These conditions are familiar to those skilled in the art in the manufacture of sulfite fiber. After the liquor has been completely neutralized, it is subjected to evaporation in cacao (28.5 inches-mercury) at a relatively low temperature, say 90 F., and the evaporation is continued until the liquor is at a specific gravity of approximately 1.3, the evaporation having the effect of driving off a large portion of the water and of the relatively volatile constituents of the liquor. At this time, the liquor is of a consistency resembling treacle, is somewhat oleaginous to the touch, and at the same time is more or less viscid and somewhat cohesive. The evaporated and neutralized liquor has now added to it a substance which, though soluble in water, is adhesive or sticky. and which will. when subjected to high heat. decompose and unite with the gases which are given off upon the decomposition of the organic compounds in the liquor. For this purpose. I utilize a soluble silicate. preferably sodium silicate, and this may be obtained on the open market at a consistency resembling molasses. Of this material I add substantially 1% to the resultant from the evaporation process. The whole is then subjected to thorough agitation and mixture to produce a substantially homogeneous mass which is sticky and of substantially the consistency of treacle. produced, may now be utilized in making cores by thoroughly mixing it with sand or I find that, by means of the compound such as described, I am able to use WIIIIIl-ll The compound, thus the former acting as a bin inexpensive sands or earths, such for instance as what 15 known as gangway sand and secure as excellent results as though ades of sands and earths were employed in making cores, and I further find that the compound may be used in the proportion of substantially 80 to 90 parts in volume of sand to 1 part in volume of the compound, whereas, so far as I am aware, the proportion' in which the best compounds now on the market are used, is 1 part to 30 parts.
After the core has been made, it is subjected to bakin in the usual manner and is thereafter su stantially impervious to water, so that there is no danger of its absorbing moisture prior to its use in casting. The baking; of'co'urse, is accomplished at high tempertures to bring the cores to red heat, and, during such baking, the sodium silicate is probably decomposed, the sodium uniting with'the sulfite gases given off by the decomposition of the organic sulfites or sulfonates of the liquor. The silicic acid higher given off during such decomposition is probdecomposed into silica and as steam and er between the sand and the organic solids of This is my theory of the act-ion althoughI have not fy it. I know as a that the results ably largely water, the latter evaporatin particles of the liquor. of the sodium silicate, been able as yet to veri practical matter, however, seem to justify the theory.
When being used in casting, the core retains its form during the initial setting of the molten metal, but due to the high temperature to which it is raised, the silicate and the organic salts, with which it is united or bonded, are ruptured, as it were, so as to destroy their cementitious qualities and the core may be removed as ordinarily. (This likewise is theoretical, but, as before stated,
the results apparently justify the theory.) As a result, t ere are no free gases given off which will cause the formation of blow holes, although as ordinarily there will be given off such gases as carbon monoxid, carbon dioxid, etc., but even these are given off in smaller quantities than heretofore where other compounds were utilized.
A compound such as herein described is not only more efiicient than those heretofore used, but is very cheap on account of the utilization of the waste liquors.
Having thus explained the nature of my said invention and described a wa of mak ing and using the same, althougi without attempting to set forth all of the forms in which it may be made or all of the modes of its use, what I claim is:
y 1. The herein described process of making core compounds, which consists in neutralizing the acids in the Waste liquors from the manufacture of sulfite fiber, evaporating the resultant at a low temperature, and mixing a soluble silicate therewith to form a homogeneous mixture.
2. The herein described process of making core compounds, which consists in neutralizing the acids in the waste liquors from the manufacture of sulfite fiber by the addition'of an alkaline base, evaporating the resultant in 'vrwuo at a temperature of approximately 90 F., and mixin sodium silicate therewith to form a iomogeneous mixture.
3. The herein described core compound which consists of a' mixture of neutralized waste liquor resulting from the manufacture of sulfite fiber and a soluble silicate.
4. The herein described core compound which consists of a homogeneous mixture of neutralized evaporated waste liquor resulting from the manufacture of sulfite fiber and sodium silicate.
In testimony whereof I have aflixed my signature, in presence of two witnesses.
HUGH K. MOORE.
Witnesses:
E. Baronnmna, P. W. Pazzm'n.
US73776212A 1912-12-19 1912-12-19 Core compound. Expired - Lifetime US1091690A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US73776212A US1091690A (en) 1912-12-19 1912-12-19 Core compound.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US73776212A US1091690A (en) 1912-12-19 1912-12-19 Core compound.

Publications (1)

Publication Number Publication Date
US1091690A true US1091690A (en) 1914-03-31

Family

ID=3159906

Family Applications (1)

Application Number Title Priority Date Filing Date
US73776212A Expired - Lifetime US1091690A (en) 1912-12-19 1912-12-19 Core compound.

Country Status (1)

Country Link
US (1) US1091690A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2549822A (en) * 1947-11-24 1951-04-24 Masonite Corp Binder for foundry compositions
US2676108A (en) * 1949-09-14 1954-04-20 Masonite Corp Process of preparing plastic substances and mold compositions and products thereof
US2861893A (en) * 1956-05-25 1958-11-25 Brumley Donaidson Co Foundry cores
US4226277A (en) * 1978-06-29 1980-10-07 Ralph Matalon Novel method of making foundry molds and adhesively bonded composites
US5590441A (en) * 1995-02-27 1997-01-07 General Motors Corporation Lift-off door hinge

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2549822A (en) * 1947-11-24 1951-04-24 Masonite Corp Binder for foundry compositions
US2676108A (en) * 1949-09-14 1954-04-20 Masonite Corp Process of preparing plastic substances and mold compositions and products thereof
US2861893A (en) * 1956-05-25 1958-11-25 Brumley Donaidson Co Foundry cores
US4226277A (en) * 1978-06-29 1980-10-07 Ralph Matalon Novel method of making foundry molds and adhesively bonded composites
US5590441A (en) * 1995-02-27 1997-01-07 General Motors Corporation Lift-off door hinge

Similar Documents

Publication Publication Date Title
US2284248A (en) Manufacture of shaped particles of hydrous alkali metal silicates
US1091690A (en) Core compound.
US617079A (en) Bone-black substitute and method of manufacture
US1467321A (en) Binder and process of making same
US1777247A (en) Porous organic material and process of producing the same
US2060311A (en) Method of making colloidal sulphur
US2445838A (en) Treatment of waste sulfite liquor
US757337A (en) Process of making adhesives.
US1895775A (en) Bituminous emulsion
US1859888A (en) Process of regenerating spent alkaline liquor to fresh acid cooking liquor
US1311216A (en) Aoobpobatxokoftcwjxrsey
US2240254A (en) Building material
US1315889A (en) Per westin
US1246806A (en) Fibrous plastic composition and process of making same.
US1428207A (en) Fire-extinguishing composition
US1425747A (en) Phosphatic fertilizer material and process of making the same
US1754842A (en) Concentrating rubber latex
US809739A (en) Adhesive and process of making same.
US747689A (en) Process of treating lime.
US611381A (en) Georg kassner
US1902106A (en) Method of manufacturing paper pulp
US547950A (en) Artificial building-block
US1231468A (en) Waterproof cement.
US1504339A (en) Manufacture of monosodium phosphate
US851378A (en) Composition of matter and process of making same.