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Publication numberUS3597158 A
Publication typeGrant
Publication dateAug 3, 1971
Filing dateJan 13, 1969
Priority dateJan 13, 1969
Publication numberUS 3597158 A, US 3597158A, US-A-3597158, US3597158 A, US3597158A
InventorsHorton Marvin Duane
Original AssigneeMegadiamond Corp
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Method of making diamonds
US 3597158 A
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Description  (OCR text may contain errors)

United States Patent fice 3,597,158 METHOD OF MAKING DIAMONDS Marvin Duane Horton, Provo, Utah, assignor to Megadiamond Corporation No Drawing. Filed Jan. 13, 1969, Ser. No. 790,866 Int. Cl. C01b 31/06 U.S. Cl. 23-209.1 1 Claim ABSTRACT OF THE DISCLOSURE Synthetic diamonds are made by mixing a carbonaceous material with an alloy consisting of about 95% nickel and 5% beryllium or 45-96% nickel and 554% zirconium, and heating the mixture at a pressure of 50,000-60,000 atmospheres to a temperature of 1200- 1350 C.

This invention relates to an improved method for converting non-diamond carbon into the diamond form.

U.S. Pats. Nos. 2,947,609, 2,947,610, 2,947,611 and 2,992,900 describe processes for transforming non-diamond carbon into diamond wherein a carbonaceous material such as graphite is mixed with a metal or metal alloy, the mixture placed in a suitable apparatus and subjected to high pressures, and the temperature raised to the melting point of the metal or its alloy. If the mixture contains a metal having a catalytic effect and the temperature and pressure conditions are such that diamond is the thermodynamically stable form of carbon, the nondiamond carbon may convert to diamond.

The rate of breakage of the costly tungsten-carbide anvils generally used to bring the graphite-metal mixture to the required pressures increases exponentially with pressure. Thus, in order to minimize wear and breakage of the anvil and otherwise reduce wear and tear on the apparatus, it is desirable that the pressure at which diamond conversion is effected be as low as possible. Alloys are particularly useful in this respect since they generally melt at a temperature lower than that of the pure metal, and the melting point of an alloy depends somewhat on the pressure of the system. Use of an alloy having the capability to yield satisfactory diamonds at a temperature even only 100 lower, and hence at final pressures 3,000 atmospheres lower, can greatly extend the working life of the anvil.

While in certain cases the use of alloys will not impair diamond production, it is most often found in practice that the dilution of a metal having the desired catalytic activity with another metal results in an alloy of activity inferior to that of the parent catalyst. I have now discovered an improved method for converting non-diamond carbon to diamond utilizing lower melting alloys which permit operation at relatively low temperatures and pressures and, at the same time, result in an increased yield of a superior diamond product.

It is, therefore, an object of the present invention to provide an improved method for converting non-diamond carbon into the diamond form at temperatures and pressures lower than those customarily employed.

It is a further object of the invention to provide a method that gives rise to increased yields of larger diamonds than can otherwise be obtained by operation at such lower temperatures and pressures.

It is yet another object of the present invention to provide a method that results in diamond crystals of more perfect shape at these milder conditions.

In accordance with these objects, the present invention is a method for making diamonds which comprises mixing a carbonaceous material with an alloy consisting of about 95 nickel and 5% beryllium or 45-96% nickel 3,597,158 Patented Aug. 3, 1971 and 4% zirconium, heating the mixture at a pressure in the range 50,000-60,000 atmospheres to a temperature in the range 12001350 C., and recovering the diamonds formed. The synthetic diamonds produced by the method of the present invention have the same utility as natural diamonds, e.g., in ornamental articles and in cutting and abrasive tools.

Graphite remains the most convenient starting material for conversion to diamond. In addition, the process of the present invention is applicable to other carbonaceous materials which undergo this conversion, e.g., amorphous carbon, carbon-containing products of nature, carbon-containing compounds of known and indeterminate structure, and the like.

The process of the present invention may be effected using any suitable apparatus capable of producing the conditions of pressure and temperature required for conversion of the carbonaceous starting material to diamond. A particularly useful apparatus is the hydraulic press described in U.S. Pat. 2,947,610, which description is incorporated herein by reference. In the experiments below, a powdered alloy mixture was prepared and used to fill a hollow graphite cylinder which was then inserted into the apparatus and subjected to the indicated pressure. The temperature was raised to the indicated value by passage of an electric current through the reaction system.

As noted above, diamond making procedures require that the metal or metal alloy be raised at least to its melting point. However, bringing the carbonaceous starting material to the diamond stable region shown in U.S. Pat. 2,947,609, even in contact with a molten alloy of a metal taught by the patent as effective for the purpose, may not always result in the desired conversion. For example, diamonds were not formed from graphite when the following alloys were heated to melting at the indicated conditions:

Pressure Temperature Approx. alloy composition (percent) (atmos) (degrees C.)

33-88 Ni, 67-12 Ge 63,000 1, 250 Mn, 40 Ge 60, 000 1, 250 60 Ni, 30 Ge 63,000 1, 500 63-80 Ni, 37-20 In 60, 000 1, 390 84 Ni, 16 Mg 61,000 1, 390 72 Mn, 28 Y 60, 000 1, 320 65 Ni, 35 Pr... 63,000 1, 450 60 Ni, 40 Sn 60, 000 1, 320 Ni, 30 Th 60, 000 1, 450 57 Ni, 43 Y 61, 000 1, 250 60 Ni, 40 Zn 63, 000 1, 450

While the diamond stable region in U.S. Pat. 2,947,609 is taught as extending above 50,000 atmospheres and 1200 C., nearly all of the working examples of the patent show pressures upwards of 63,000 atmospheres and temperatures upwards of 1350 C. Only manganesenickel alloy (60:40 eutectic) appears effective as a conversion catalyst in the 50,000-60,000 atmosphere pressure range and at temperatures below 1350 C.

Using the following nickel-beryllium or nickel-zirconium alloys:

Approx. alloy composition: Melting point, C. Ni, 5% Be 1200 4596% Ni, 55-4% Zn 1100-1250 I am able to produce diamonds at pressures of 60,000 atmospheres or below and at temperatures of 1350 C. or below. Further, utilization of these alloys in the conversion of carbonaceous material to diamond at such milder conditions unexpectedly gives rise to an increased yield of larger and more perfectly shaped diamonds than obtained by using an operative alloy of U.S. Pat. 2,947,609, i.e., manganese-nickel.

Mixtures of graphite and the test alloy were placed in the graphite cylinder, brought to the indicated pressure in the hydraulic press, and the alloy melted by passing an alternating current longitudinally through the graphite-alloy mixture. After cooling and depressurization, the diamonds produced were separated and examined. The results are summarized below:

Approx. alloy Diamond composition Pressure Temperature Run time yield (percent) (atmos) (degrees 0,) (min.) (mg) 60 Mn, 40 Ni 56, 000 1, 350 6 3. 7 95 Ni, Be 56, 000 1,350 6 32. 0 60 Mn, Ni 60,000 1, 200 3 3. 5 Ni, 50 Zr t- 60, 000 l, 200 3 25. 8

As shown, the use of nickel-beryllium and nickelzirconium alloys result in the formation of larger quantities of diamond than obtained with manganese-nickel alloy under comparable conditions. It was also found that use of these alloys produced more nearly perfect diamond crystals as determined visually by comparing the many excellent crystalline faces produced with these alloys contrasted with the few clearly defined crystal faces produced with manganese-nickeL It was further characteristic of these alloys that their use resulted in diamonds larger than those obtained using manganese-nickel alloy as summarized below:

Approxalloy Temperature Pressure Average crystal Composition (percent) (degrees C.) (atmos) diameter (mm.)

Mn, 40 Ni- 1, 320 56, 000 O. 2 Ni, 5 Be 1, 320 56, 000 0. 5 60 Mn, 40 Ni- 1, 200 60,000 0. 2 50 Ni, 50 Zr 1, 200 60, 000 0. 7

References Cited UNITED STATES PATENTS 8/1960 Strong 23-209.1 7/1961 Bovenkerk 23209.1

OTHER REFERENCES Kirk-Othmer Encyclopedia of Chemical Technology, vol. 3, 1964, pp. 451-452.

EDWARD J. MEROS, Primary Examiner

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4005180 *Jan 24, 1975Jan 25, 1977De Beers Industrial Diamond Division LimitedFrom hexachlorobenzene, hexachloroethane, tetrachloroquinone
US4406871 *May 30, 1980Sep 27, 1983Samoilovich Mikhail IProcess for growing diamonds
US6402787Jan 30, 2000Jun 11, 2002Bill J. PopeProsthetic hip joint having at least one sintered polycrystalline diamond compact articulation surface and substrate surface topographical features in said polycrystalline diamond compact
US6494918Jan 30, 2000Dec 17, 2002Diamicron, Inc.Component for a prosthetic joint having a diamond load bearing and articulation surface
US6514289Jan 30, 2000Feb 4, 2003Diamicron, Inc.Diamond articulation surface for use in a prosthetic joint
US6517583Jan 30, 2000Feb 11, 2003Diamicron, Inc.Prosthetic hip joint having a polycrystalline diamond compact articulation surface and a counter bearing surface
US6596225Jan 31, 2000Jul 22, 2003Diamicron, Inc.Methods for manufacturing a diamond prosthetic joint component
US6676704Jan 30, 2000Jan 13, 2004Diamicron, Inc.Prosthetic joint component having at least one sintered polycrystalline diamond compact articulation surface and substrate surface topographical features in said polycrystalline diamond compact
US6709463Jan 30, 2000Mar 23, 2004Diamicron, Inc.Prosthetic joint component having at least one solid polycrystalline diamond component
US6793681Jan 30, 2000Sep 21, 2004Diamicron, Inc.Prosthetic hip joint having a polycrystalline diamond articulation surface and a plurality of substrate layers
US6800095Jan 30, 2000Oct 5, 2004Diamicron, Inc.Diamond-surfaced femoral head for use in a prosthetic joint
US7077867Jan 30, 2000Jul 18, 2006Diamicron, Inc.Prosthetic knee joint having at least one diamond articulation surface
US7396501Aug 27, 2004Jul 8, 2008Diamicron, Inc.Use of gradient layers and stress modifiers to fabricate composite constructs
US7396505Aug 27, 2004Jul 8, 2008Diamicron, Inc.Use of CoCrMo to augment biocompatibility in polycrystalline diamond compacts
US7494507Aug 28, 2002Feb 24, 2009Diamicron, Inc.Articulating diamond-surfaced spinal implants
US7556763Aug 28, 2004Jul 7, 2009Diamicron, Inc.mixing a carbide of Ti or Nb with TiC, enclosing mixture in a niobium can, pressing it into a spherical component by hot isostatic pressing; superhard
US7569176Aug 28, 2004Aug 4, 2009Diamicron, Inc.Hardness; sintering; by-product free; nontoxic
US7665898Oct 21, 2008Feb 23, 2010Diamicron, Inc.Bearings, races and components thereof having diamond and other superhard surfaces
US7678325Apr 5, 2006Mar 16, 2010Diamicron, Inc.Use of a metal and Sn as a solvent material for the bulk crystallization and sintering of diamond to produce biocompatbile biomedical devices
US8016889Dec 14, 2007Sep 13, 2011Diamicron, IncArticulating diamond-surfaced spinal implants
US8449991Apr 10, 2009May 28, 2013Dimicron, Inc.Use of SN and pore size control to improve biocompatibility in polycrystalline diamond compacts
US8603181Apr 8, 2010Dec 10, 2013Dimicron, IncUse of Ti and Nb cemented in TiC in prosthetic joints
US8663359Jun 25, 2010Mar 4, 2014Dimicron, Inc.Thick sintered polycrystalline diamond and sintered jewelry
Classifications
U.S. Classification423/446
International ClassificationB01J3/06
Cooperative ClassificationB01J2203/061, B01J2203/0655, B01J2203/0625, B01J2203/068, B01J3/062
European ClassificationB01J3/06B