US2136931A - Method of making abrasive articles - Google Patents

Method of making abrasive articles Download PDF

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Publication number
US2136931A
US2136931A US163436A US16343637A US2136931A US 2136931 A US2136931 A US 2136931A US 163436 A US163436 A US 163436A US 16343637 A US16343637 A US 16343637A US 2136931 A US2136931 A US 2136931A
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United States
Prior art keywords
amalgam
metal
abrasive articles
metals
bond
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Expired - Lifetime
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US163436A
Inventor
Raymond C Benner
George J Easter
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Unifrax 1 LLC
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Carborundum Co
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Publication date
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Priority to US163436A priority Critical patent/US2136931A/en
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/14Anti-slip materials; Abrasives
    • C09K3/1436Composite particles, e.g. coated particles
    • C09K3/1445Composite particles, e.g. coated particles the coating consisting exclusively of metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D18/00Manufacture of grinding tools or other grinding devices, e.g. wheels, not otherwise provided for

Definitions

  • One of the main objects of this invention is the metallic bonding of diamond particles in such a way that the diamond particles are more completely wetted by the bond and a resulting article obtained of improved cutting ability and characteristics, as well as prolonged life.
  • We accomplish this by the use of metal amalgams as the wetting and bonding materials for the dia- 'monds according to the methods herein set forth,
  • Another important feature of the present invention is the provision as a wetting and bonding material for diamonds of an amalgam relatively inexpensive and therefore extremely economical for general industrial or commercial application.
  • the amalgams which we use can all be easily made by simple intimate admixing of the metal or metals with mercury, although due to the difliculty of obtaining some of the metals in powdered form we usually prefer to carry out the amalgamation indirectly by electrolytic decomposition of the metallic salts of-the metal which we desire to amalgamate using mercury as a cathode or a similar decomposition of a mercury salt using the metal as'a cathode, depending upon the availability of the respective raw materials.
  • Numerous other methods of obtaining the amal- More particugams may be used, but the above two general methods, especially the electrolytic method, are given as examples because of their simplicity and their applicability to practically all of the amalgams we may care to make.
  • amalgams we use additional mercury over that required to form the solid amalgam-of the metal and sufiicient to obtain an amalgam in pasty or. semi-liquid condition, often containing excess mercury.
  • the amalgam is usually made up in small quantities just prior to use, we sometimes have found occasion to make it up some in which event it.is desirable to maintain the amalgam under electrolytic potential to prevent its deterioration in any way before use.
  • Some of the metals which .we are able to amalgamate by one or more of these methods are potassium, sodium, barium, calcium, zinc, tin, lead, bismuth, copper, antimony, silver and gold.
  • Theamalgams which we use are. usually combinations of more than one of the above metals in which case we generally proceed by successive electrolytic amalgamation of the various constituent metals of the desired final amalgam.
  • the second metal to be amalgamated is then placed-in the same amalgamation chamber as the cathode and the operating conditions readjusted to those best suited for its amalgamation and the operations resumed until the.
  • non-metallic abrasive particles with a wettingout agent which assists the wetting of said particles by amalgams coating said abrasive particles with an amalgam, thereafter mixing the amalgam-coated particles with additional metallic bond free from. mercury to form an abrasive mixture, pressing and sintering said mixture to the 5 desired shape.

Description

Patented Nov. 15, 1938 UNITED STATES PATENT OFFICE METHOD OF MAKING ABRASIVE ARTICLES Raymond C. Benner and George J. Easter, Niagara Falls, N. Y., assignors to The Carbon!!!- dum Company, Niagara Falls,
tion of Delaware N. Y., a corpora- No Drawing. Application September 11, 1937,
- Serial No. 163,436
3 Claims.
that it is extremely diflicult to obtain a good bond for diamonds. This is largely due to the difficulty of obtaining a bond which will thoroughly wet or coat the surface of the diamond particles and consequently promote the close adherence or adhesiveness between the abrasive and the bond. In the use of metal in its powdered or cast form, the adhesion between bond and diamond has never been as satisfactory as might be desired. The diamond particles have not been thoroughly wetted and have to a large extent been merely gripped by the surrounding metal bond without complete wetting of the interfaces taking place. Articles so made therefore have not shown the high efliciencies and durability which are so much to be desired.
One of the main objects of this invention-is the metallic bonding of diamond particles in such a way that the diamond particles are more completely wetted by the bond and a resulting article obtained of improved cutting ability and characteristics, as well as prolonged life. We accomplish this by the use of metal amalgams as the wetting and bonding materials for the dia- 'monds according to the methods herein set forth,
which methods play an important part in the successful formation of such articles.
Another important feature of the present invention is the provision as a wetting and bonding material for diamonds of an amalgam relatively inexpensive and therefore extremely economical for general industrial or commercial application. For this purpose we make use of amalgams containing substantial amounts of base metals, and at times even the amalgam is composed entirely of base metals.
The amalgams which we use can all be easily made by simple intimate admixing of the metal or metals with mercury, although due to the difliculty of obtaining some of the metals in powdered form we usually prefer to carry out the amalgamation indirectly by electrolytic decomposition of the metallic salts of-the metal which we desire to amalgamate using mercury as a cathode or a similar decomposition of a mercury salt using the metal as'a cathode, depending upon the availability of the respective raw materials. Numerous other methods of obtaining the amal- More particugams may be used, but the above two general methods, especially the electrolytic method, are given as examples because of their simplicity and their applicability to practically all of the amalgams we may care to make. In forming the amalgams we use additional mercury over that required to form the solid amalgam-of the metal and sufiicient to obtain an amalgam in pasty or. semi-liquid condition, often containing excess mercury. Although the amalgam is usually made up in small quantities just prior to use, we sometimes have found occasion to make it up some in which event it.is desirable to maintain the amalgam under electrolytic potential to prevent its deterioration in any way before use.
Some of the metals which .we are able to amalgamate by one or more of these methods are potassium, sodium, barium, calcium, zinc, tin, lead, bismuth, copper, antimony, silver and gold. Theamalgams which we use are. usually combinations of more than one of the above metals in which case we generally proceed by successive electrolytic amalgamation of the various constituent metals of the desired final amalgam. In this process after amalgamation of one of the metals for a predetermined period of time the first constituent metal to'be amalgamated and which has acted during its amalgamation as the cathode is removed, the second metal to be amalgamated is then placed-in the same amalgamation chamber as the cathode and the operating conditions readjusted to those best suited for its amalgamation and the operations resumed until the.
desired amount of this metal is present in the amalgam. After all of the desired constituent metals have served as cathodes for the periods necessary to amalgamate the required amounts of each metal desired to be in the final alloyamalgam, the operation is complete. During the later portion of the operation, as the amalgam becomes pasty rather than fluid, it is desirable to employ mechanical stirring'of the amalgam more or less continuously in order to cause the depositing metal to be dispersed evenly throughout the amalgam rather than plated onto it as a separate surface layer. Heat may also be applied as required to keep the amalgam workable at concentrations which result in the formation of a powderable texture when cold. This electrolytic process of amalgamation is quantitatively very accurate and practically any desired composition of alloy-amalgam may be obtained in this way.
' After the amalgam has been made and is ready to use in paste or liquid form, we then thoroughly mix into the mass a quantity of diamond particles, continuing the mixing until we are sure the diamonds are uniformly distributed throughout the amalgam. Instead of using diamonds as the tinie before using it as the bond br wetting agent,
coating the diamond particles with a silver-copper amalgam, thereafter adding metal powder free from mercury to the coated diamonds and molding and sintering the mass to shape.
3. The process of manufacturing metal-bonded abrasive articles which comprises moistening.
non-metallic abrasive particles with a wettingout agent which assists the wetting of said particles by amalgams, coating said abrasive particles with an amalgam, thereafter mixing the amalgam-coated particles with additional metallic bond free from. mercury to form an abrasive mixture, pressing and sintering said mixture to the 5 desired shape. 7
RAYMOND C. BENNER. GEORGE J. EASTER.
US163436A 1937-09-11 1937-09-11 Method of making abrasive articles Expired - Lifetime US2136931A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2562587A (en) * 1948-07-19 1951-07-31 Ind Res And Engineering Compan Bonded abrasive

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2562587A (en) * 1948-07-19 1951-07-31 Ind Res And Engineering Compan Bonded abrasive

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