Title of Invention

A METHOD OF CHANGING THE COLOUR OF A BROWN TYPE II DIAMOND FROM BROWN TO PINK

Abstract The present invention relates to a method of changing the colour of a brown type II diamond from brown to pink comprises the steps of: j) creating a reaction mass by providing the diamond in a pressure transmitting medium which completely encloses the diamond, and ii) subjecting the reaction mass to a temperature in the range of 1900°C to 2300°C, under a pressure of 6.9 GPa to 8.5 GPa .
Full Text

This invention relates to a method of changing the colour of diamond.
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Diamonds are generally classified into four main types: la, lb, lla and lib. These types are usually distinguished by infrared and ultraviolet spectra. Type la and lb diamonds contain nitrogen in a combination of different forms. Type lb contains single substitutional nitrogen or C-centres. la contains a combination of various nitrogen structures. Type lla diamonds have a nitrogen content of less than a few parts per million (ppm) and can be defined as those diamonds which show substantially no absorption in the 1332-400 cm"1 range when irradiated with infrared radiation. Type lla diamond can exhibit a brown colour caused, it is believed, by structural deformation within the diamond crystal lattice.
US 4,124,690 describes a process for converting type lb nitrogen into type la nitrogen in type lb diamond by high temperature annealing under a pressure which prevents graphitisation. This treatment has the effect of reducing the yellow colour of the type lb diamond.

SUMMARY OF THE INVENTION
According to the present invention there is provided a method of changing the colour of a brown type lla diamond from brown to pink which includes the steps of:
(i) creating a reaction mass by providing the diamond in a pressure
transmitting medium which completely encloses the diamond,
and (ii) subjecting the reaction mass to a temperature in the range of
1900°C to 2300°C, under a pressure of 6,9GPa to 8,5GPa for a
suitable period of time.
DESCRIPTION OF EMBODIMENTS
In the present invention, a brown type lla diamond crystal, which will generally be natural diamond, is annealed under a pressure which prevents significant graphitisation in order to modify the structural deformation which gives rise to the brown colouration and thereby reduce the brown colour and produce or enhance the pink colour of the diamond. A pink diamond is produced.
Pink natural diamonds are rare. Thus, the present invention provides a method of producing or enhancing the pink colour of a natural type lla diamond without causing damage to the diamond crystal.
The typical infrared absorption spectrum of a type lla diamond is shown in Figure 1. However, it is not all type lla diamonds which are suitable for colour enhancement by high temperature and high pressure treatment of the present invention. The diamonds must have a brown colour which can vary from deep to light brown, including e.g. pinkish brown. Those type ila diamonds that are most suitable for the present invention have a nitrogen concentration of less

than 2 ppm, preferably less than 0,2 ppm, exhibit a brown to pinkish brown colour and have a typical ultraviolet / visible absorption spectrum as shown in Figure 2 in graph line a, which shows a monotonically rising absorption, or a monotonically rising absorption with broad bands centred about 390 and 550 nm as shown in Figure 2 in graph line b.
The brown diamond is converted to a pink diamond using an annealing temperature ranging from about 1900°C to about 2300°C, and preferably 2100°C to 2300°C, under a pressure ranging from 6,9GPa to 8,5GPa and preferably about 7,4GPa to 8,5GPa, for a period generally ranging from 10 minutes to 10 hours, and preferably 20 minutes to 4 hours. Generally, the higher the annealing temperature, the shorter the annealing time. Examples of particularly suitable annealing conditions, within the pressure ranges identified above are:
2200 - 2300°C for 1 hour
2300°C for a period of less than 4 hours and preferably 1 hour.
2100°Cfor1 hour.
The change in colour of the type Ha diamond crystal can be quantified by the changes in the absorption spectrum of the crystal taken before and after annealing. Spectra are taken of the crystal at room temperature by means of a spectrometer in a conventional manner showing the ultraviolet / visible absorption spectrum of the crystal. After the crystal is annealed, spectra are taken of it again at room temperature.
Subjecting such diamonds to the method of this invention results in a reduction of strength of the monotonically rising absorption and the production or the enhancement of the strength of the broad absorption bands at 390 and 550 nm; this results in the enhanced pink colour.

In the method of the invention, a reaction mass is created by providing diamond in a pressure transmitting medium which completely encloses a diamond. The pressure transmitting medium is preferably a homogeneous pressure transmitting medium which evenly spreads the pressure which is applied over the entire surface of the diamond which is being treated. Examples of suitable mediums are those which have a low shear strength such as metal halide salts. Examples of suitable metal hatide salts are potassium bromide, sodium chloride, potassium chloride, caesium chloride, caesium bromide, copper chloride and copper bromide. Such mediums have been found to provide the desirable even spread of pressure which ensures that any graphitisation which may occur on the diamond surface is kept to a minimum. A particular advantage of using a metal halide salt as the pressure transmitting medium is that the diamonds can be easily recovered after treatment by dissolving the medium in hot water.
The method of the invention may be used to treat a single diamond or a plurality of discrete diamonds. If a plurality of discrete diamonds are treated simultaneously, each diamond should be separated from its neighbours by the pressure transmitting medium. The maximum volume of diamond which may be treated is limited only by the capacity of the high pressure/high temperature apparatus used.
Conventional high temperature/high pressure apparatus may be used in the method of the invention. Various reaction vessel configurations which provide for indirect or direct heating of the reaction mass are disclosed in the patent literature and are useful in carrying out the present annealing process. These reaction vessels usually consist of a plurality of interfitting cylindrical members and end plugs or discs for containing the reaction mass in the centremost cylinder. In the indirectly heated type of reaction vessel one of the cylindrical members is made of graphite which is heated by the passage of electric current therethrough and which thereby heats the reaction mass. In the

directly heated type of reaction vessel, the reaction mass is electrically conductive, thereby eliminating the need for an electrically conductive graphite cylinder, and electric current is passed directly through the reaction mass to heat it.
The invention is illustrated by the following example.
EXAMPLE 1
A natural brown type Ha diamond, with the ultraviolet / visible absorption spectrum before treatment shown in Figure 3 in graph line a, was used. A plurality of such diamonds were placed in a pressure transmitting medium in a reaction vessel of the type illustrated by Figure 4. Referring to this figure, the diamond crystals 10 are placed in a pressure transmitting medium 12 such that the crystals are discrete and separated from each other in the pressure transmitting medium. The diamonds are preferably evenly dispersed in the medium. The pressure transmitting medium is preferably a low shear strength medium of the type described above. The diamond-containing medium 12 is placed in a container 14 made from graphite, pyrophyllite, magnesium oxide or zirconium oxide which is enclosed by co-operating metal cups 16, 18 which form a metal canister around the container 14. The metal may be molybdenum, tantalum or steel. The canister may be compacted around the container to eliminate air voids. The loaded canister is now placed in the reaction zone of a conventional high temperature/high pressure apparatus. The contents of the capsule were subjected to a temperature of 2250°C and a pressure of 7,8GPa which conditions were maintained for a period of 4 hours. The capsule was removed from the apparatus and allowed to cool. The canister and graphite container were removed and the diamonds recovered from the medium. The ultraviolet / visible absorption spectrum of the diamond after treatment is shown in Figure 3 in graph line b. The spectrum shows the

presence of the broad bands at 390 and 550 nm which gives rise to pink colouration which was observed.
The Co-Pending Application No: IN/PCT/2002/01584/CHE relates to a method of changing to blue or enhancing the colour of a type 11b diamond comprising the steps of:(i) creating a reaction mass by providing the diamond in a pressure transmitting medium which completely encloses the diamond, and(ii) subjecting the reaction mass to a temnerature in the ranee 1800°C to 2600°C under a pressure of 6.7 GPa to 9 GPa.



WE CLAIM:
1. A method of changing the colour of a brown type II diamond from brown to
pink comprising the steps of:
i) creating a reaction mass by providing the diamond in a pressure transmitting medium which completely encloses the diamond, and
ii) subjecting the reaction mass to a temperature in the range of 1900°C to 2300°C, under a pressure of 6.9 GPa to 8.5 GPa .
2. The method as claimed in claim 1, wherein the diamond is natural diamond.
3. The method as claimed in claim 1 or claim 2, wherein the diamond has a nitrogen concentration of less than 2 ppm5 exhibits brown to pinkish brown colour and has an ultraviolet/visible absorption spectrum which shows a monotonically rising absorption, or a monotonically rising absorption with broad bands centred about 390 and 550 nm.
4. The method as claimed in claim 3, wherein the nitrogen concentration is less than 0.2 ppm.
5. The method as claimed in any one of the preceding claims, wherein the diamond, after being subjected to step (ii), has a reduction of strength of the monotonically rising absorption, and a production or enhancement of the strength of a broad absorption band at 390 and 550 nm.
6. The method as claimed in any one of the preceding claims, wherein the

temperature in step (ii) is in the range 2100°C to 2300°C.
7. The method as claimed in any one of the preceding claims, wherein the pressure in step (ii) is in the range 7.4 GPa to 8.5 GPa.
8. The method as claimed in any one of the preceding claims, wherein the period during which the diamond is subjected to the conditions of step (ii) is in the range 10 minutes to 10 hours.
9. The method as claimed in claims 1 to 7, wherein the period during which the diamond is subjected to the conditions of step (ii) is in the range 20 minutes to 4 hours.
10. The method as claimed in any one of the preceding claims, wherein a plurality of diamonds is placed in the pressure transmitting medium, each diamond being separated from its neighbour by pressure transmitting medium.
11. The method as claimed in any one of the preceding claims, wherein the pressure transmitting medium is a homogeneous medium which completely encloses the or each diamond and is applied over the entire surface of the or each diamond.

12. The method as claimed in any one of the preceding claims, wherein the pressure transmitting medium has a low shear strength.
13. The method as claimed in any one of the preceding claims, wherein the pressure transmitting medium is water soluble.

14. The method as claimed in any one of the preceding claims, wherein the
pressure transmitting medium is a metal halide salt.
15. The method as claimed in claim 14, wherein the halide is chloride or bromide.
16. The method as claimed in any of claims 1 to 11, wherein the pressure transmitting medium is potassium bromide.
17. The method as claimed in any of claims 1 to 11, wherein the pressure transmitting medium is sodium chloride.
18. The method as claimed in any of claims 1 to 11, wherein the pressure transmitting medium is potassium chloride.
19. The method as claimed in any of claims 1 to 11, wherein the pressure transmitting medium is caesium chloride.
20. The method as claimed in any of claims 1 to 11, wherein the pressure transmitting medium is caesium bromide.
21. The method as claimed in any of claims 1 to 11, wherein the pressure transmitting medium is copper chloride.
22. The method as claimed in any of claims 1 to 11, wherein the pressure transmitting medium is copper bromide.

23. A method of changing the colour of a brown type II diamond from brown to pink substantially as in described with reference to the accompanying drawings.


Documents:

in-pct-2002-1585-che claims duplicate.pdf

in-pct-2002-1585-che descripition(completed) duplicate.pdf

in-pct-2002-1585-che drawings duplicate.pdf

in-pct-2002-che-1585-abstract.pdf

in-pct-2002-che-1585-assignment.pdf

in-pct-2002-che-1585-claims duplicate.pdf

in-pct-2002-che-1585-claims original.pdf

in-pct-2002-che-1585-correspondance others.pdf

in-pct-2002-che-1585-correspondance po.pdf

in-pct-2002-che-1585-description complete duplicate.pdf

in-pct-2002-che-1585-description complete original.pdf

in-pct-2002-che-1585-drawings.pdf

in-pct-2002-che-1585-form 1.pdf

in-pct-2002-che-1585-form 26.pdf

in-pct-2002-che-1585-form 3.pdf

in-pct-2002-che-1585-form 5.pdf

in-pct-2002-che-1585-other documents.pdf

in-pct-2002-che-1585-pct.pdf


Patent Number 205909
Indian Patent Application Number IN/PCT/2002/1585/CHE
PG Journal Number 26/2007
Publication Date 29-Jun-2007
Grant Date 12-Apr-2007
Date of Filing 30-Sep-2002
Name of Patentee M/S. ELEMENT SIX (PROPRIETARY)LIMITED
Applicant Address 1 DEBID ROAD,NUFFIELD,SPRINGS, 1559 GAUTENG
Inventors:
# Inventor's Name Inventor's Address
1 BURNS, Robert, Charles 15 Los Angeles Drive, 2195 Northcliff
2 FISHER, David 6 Lancaster Road, Maidenhead, Berkshire SL6 5EP
3 SPITS, Raymond, Anthony 7 Allan Road, 2194 Bordeaux
PCT International Classification Number B01J 3/06
PCT International Application Number PCT/IB2001/000525
PCT International Filing date 2001-04-02
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 0007887.3 2000-03-31 U.K.