USH649H - Preparing titanium nitride powder - Google Patents
Preparing titanium nitride powder Download PDFInfo
- Publication number
- USH649H USH649H US07/207,806 US20780688A USH649H US H649 H USH649 H US H649H US 20780688 A US20780688 A US 20780688A US H649 H USH649 H US H649H
- Authority
- US
- United States
- Prior art keywords
- sub
- tio
- tin
- reaction
- titanium
- 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.)
- Abandoned
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/06—Binary compounds of nitrogen with metals, with silicon, or with boron, or with carbon, i.e. nitrides; Compounds of nitrogen with more than one metal, silicon or boron
- C01B21/076—Binary compounds of nitrogen with metals, with silicon, or with boron, or with carbon, i.e. nitrides; Compounds of nitrogen with more than one metal, silicon or boron with titanium or zirconium or hafnium
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/50—Agglomerated particles
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
Definitions
- This invention is a process for making TiN powder from boron phosphate, titanium oxide and sodium cyanide and was developed pursuant to a contract with the U.S. Department of Energy.
- Titanium nitride is a compound having a high melting point of 2950° C., a hardness of 8-9 in Moh's scale, exhibits good electrical conductance and is stable at high temperatures in inert atmospheres. It is known that sodium cyanide reacts at high temperatures with oxides such as BPO 4 , SiO 2 and TiO 2 to yield, respectively, BN, Si C and TiN and sodium salts of oxyanions. However, in the process of forming TiN from TiO 2 , salts such as Na 2 Ti 6 O 13 and Na 8 Ti 5 O 14 are also formed which are difficult to separate from TiN, the product of interest. Therefore there is a need to develope a process for making TiN that does not produce byproducts that interfere with obtaining the final product.
- the process of this invention may comprise mixing one or more phosphates of Ti with a cyanide salt in the absence of oxygen and heating to a temperature sufficient to cause reaction to occur.
- the ratio of cyanide salt to Ti should be at least 2 which results in the major Ti-containing product being TiN rather than sodium titanium phosphate byproducts.
- the process is an improvement over prior processes since the byproducts are water soluble salts of sodium which can easily be removed from the preferred TiN product by washing.
- Titanium phosphates TiP 2 O 7 and (TiO) 2 P 2 O 7 were prepared by reacting TiO 2 , anatase, with BPO 4 at about 1100° C. The byproduct B 2 O 3 was removed by dissolution with water and the residue was washed with acetone and dried at 120° C.
- TiN product When titanium phosphates TiP 2 O 7 and (TiO) 2 P 2 O 7 were mixed with NaCN and heated to about 1000° C. a TiN product was obtained. With an NaCN to Ti ratio of about 1 the reaction led to the formation of small amounts of TiN while forming primarily other compounds of titanium. Some of the compounds such as Na 0 .23 TiO 2 (titanium bronze) and NaTi 2 (PO 4 )3 were identifiable by x-ray diffraction (XRD) by comparing with data in the literature. It should be noted that in some instances XRD identified the titanium bronze as Na 2 Ti 2 Ti 6 O 16 (Na 0 .25 TiO 2 ).
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
A process for making titanium nitride powder by reaction of titanium phosphates with sodium cyanide.
Description
This invention is a process for making TiN powder from boron phosphate, titanium oxide and sodium cyanide and was developed pursuant to a contract with the U.S. Department of Energy.
Titanium nitride is a compound having a high melting point of 2950° C., a hardness of 8-9 in Moh's scale, exhibits good electrical conductance and is stable at high temperatures in inert atmospheres. It is known that sodium cyanide reacts at high temperatures with oxides such as BPO4, SiO2 and TiO2 to yield, respectively, BN, Si C and TiN and sodium salts of oxyanions. However, in the process of forming TiN from TiO2, salts such as Na2 Ti6 O13 and Na8 Ti5 O14 are also formed which are difficult to separate from TiN, the product of interest. Therefore there is a need to develope a process for making TiN that does not produce byproducts that interfere with obtaining the final product.
In view of the above need, it is an object of this invention to provide a process for making TiN but not interfering byproducts.
It is another object of this invention to provide a process for preparing TiN which produces no byproducts that cannot be removed by dissolution in water. Additional objects, advantages and novel features of the invention will be set forth in part in the description which follows, and in part will become apparent to those skilled in the art upon examination of the following or may be learned by practice of the invention. The objects and advantages of the invention may be realized and attained by means of the instrumentalities and combinations particularly pointed out in the appended claims.
To achieve the foregoing and other objects and in accordance with the purpose of the present invention, as embodied and broadly described herein, the process of this invention may comprise mixing one or more phosphates of Ti with a cyanide salt in the absence of oxygen and heating to a temperature sufficient to cause reaction to occur. In the preferred embodiment the ratio of cyanide salt to Ti should be at least 2 which results in the major Ti-containing product being TiN rather than sodium titanium phosphate byproducts. The process is an improvement over prior processes since the byproducts are water soluble salts of sodium which can easily be removed from the preferred TiN product by washing.
Since sodium salts are generally water soluble, applicant decided to try to prepare TiN with starting materials that would result in sodium salt byproducts that would be amenable to removal using a water wash. Applicant had previously prepared boron nitride by reaction of sodium cyanide and boron phosphate; therefore, an attempt was made to use a similar reaction with phosphates of titanium. Since boron and titanium are no chemically similar one cannot predict the behavior of titanium compounds by the behavior of corresponding boron compounds. Also, the free energies of TiN and TiC are not far enough apart to be able to predict the product of the reaction. As a matter of fact, it would not have been surprising to obtain TiCN as the product.
Titanium phosphates TiP2 O7 and (TiO)2 P2 O7 were prepared by reacting TiO2, anatase, with BPO4 at about 1100° C. The byproduct B2 O3 was removed by dissolution with water and the residue was washed with acetone and dried at 120° C.
When titanium phosphates TiP2 O7 and (TiO)2 P2 O7 were mixed with NaCN and heated to about 1000° C. a TiN product was obtained. With an NaCN to Ti ratio of about 1 the reaction led to the formation of small amounts of TiN while forming primarily other compounds of titanium. Some of the compounds such as Na0.23 TiO2 (titanium bronze) and NaTi2 (PO4)3 were identifiable by x-ray diffraction (XRD) by comparing with data in the literature. It should be noted that in some instances XRD identified the titanium bronze as Na2 Ti2 Ti6 O16 (Na0.25 TiO2). A comparison of the XRD patterns available for three titanium bronzes shows significant similarities and suggests that there is some ambiguity with respect to the exact stoichiometry of these compounds. Some other products of the reaction were not identifiable by XRD and consequently a research program aimed at their synthesis and characterization was initiated. This led to the identification of two novel compounds, Na4 (TiO)(PO4)2 and Na(TiO)PO4.
It was necessary to maintain an excess of NaCN, at least at a 2 to 1 ratio, in order to get a sufficient TiN yield and the higher the NaCN concentrations, the better the yield. The sodium phosphate by-products were easily removed by dissolving in water. Another important parameter was the length of time of heating at 1000° C.; exploratory experiments revealed that about 20 hours was sufficient for 300 mg of NaCN to completely react and/or decompose. Thus, this length of time was arbitrarily adopted for all experiments.
Results from reactions with NaCN to Ti ratios at greater than 2 indicated that the major Ti-containing product was TiN. The stoichiometries of the reactions occurring at 1000° C. between TiP2 O7 or (TiO)2 P2 O7 and increasing amounts of NaCN were estimated on the basis of identification by XRD and Raman spectroscopy of solid products as major phases and the measured amounts of carbon dioxide evolved. Additionally, the presence of Na2 C2 condensed in the cooler part of the apparatus was confirmed, on reaction with water, by the characteristic odor of gas released (similar to industrial C2 H2 containing traces of PH3), the high alkalinity of the resulting solution and the occasional spontaneous ignition of evolving acetylene. The evolution of phosphorous was confirmed by the presence of Ni2 P, identified by XRD. When TiN and Na0.23 TiO2 were present in concentrations below limits of detection of XRD and Raman spectroscopy, they were identified by optical microscopy as gold and dark blue crystals, respectively. Other unidentified products (N, CO, P) and solid products present as minor phases were inferred from material balance of the elements. The amount of each product, given in moles in Table 1, was estimated by iterative calculations which used, as input, the data of measured weight losses from the reaction and from water extraction of products.
TABLE 1
__________________________________________________________________________
Amounts of products calculated for the reaction of NaCN with various
titanium phosphates
Reaction
Titanium
NaCN to
No. compound
Ti ratio
TiN
Na.sub.3 PO.sub.4
CO.sub.2
Na.sub.2 C.sub.2
N.sub.2
P C Na.sub.4 (TiO)(PO.sub.4).sub.2
Na.sub.0.23 TiO.sub.2
CO
__________________________________________________________________________
1* TiP.sub.2 O.sub.7
1 0.05
0.06 0.35
0 0.48
0.54
0.29
0.10 0.05 0.36
2** TiP.sub.2 O.sub.7
2 0.50
0.15 0.37
0 0.75
1.09
0 0.38 0.12 2.00
3 TiP.sub.2 O.sub.7
4 1.00
1.33 0.50
0 1.50
0.67
2.82
0 0 0.68
4*** (TiO).sub.2 P.sub.2 O.sub.7
1 0 0 0.60
0 1 1.08
0.72
0.36 1.64 0.68
5 (TiO).sub.2 P.sub.2 O.sub.7
2 1.85
1.25 0.40
0 1.08
0.65
1.05
0.05 0.10 2.55
6 (TiO).sub.2 P.sub.2 O.sub.7
3 2.00
1.75 1.00
0.38
2.00
0.25
4.24
0 0 0
7.sup.§
(TiO).sub.2 P.sub.2 O.sub.7
4 2.00
1.40 0.40
1.63
2.73
0.60
1.20
0 0 2.60
8 Na.sub.4 (TiO) (PO.sub.4).sub.2
3 1.00
1.80 0.40
0.80
1.00
0.20
0 0 0 1.00
9 NaTi.sub.2 (PO.sub.4).sub.3
2 2.00
.sup.§§
2.00
0.50
1.00
1.00
0 0 0 1.00
__________________________________________________________________________
*0.40 NaTi.sub.2 (PO.sub.4).sub.3 also present among products.
**Includes 0.37 C as reactant from container.
***0.20 NaPO.sub.3 also present among products.
.sup.§ 0.54 NaCN also present among products.
.sup.§§ Found as 1.00 Na.sub.4 P.sub.2 O.sub.7 (═Na.sub.3
PO.sub.4 + NaPO.sub.3).
Although these calculated amounts are being reported to the second decimal place this was done for calculational purposes only and should not be taken as an indication of accuracy with which they are known. The state of knowledge concerning the species present (identified and inferred) and their respective amounts, can be surmised from the data in Table 2 in which the comparison is made between the measured and calculated values of weight losses from the reaction and from water extraction of the products. Taking into consideration that the studied reactions are time dependent and involve a large number of products, the agreement between those values is quite satisfactory.
TABLE 2
______________________________________
Typical calculated and measured values of weight loss from the
reaction and by water extraction of reaction products for reactions
of NaCN with titanium phosphates
% Weight loss by water
% Weight loss extraction of
Reaction No.
on reaction reaction products
(in Table 1)
Calculated
Measured Calculated
Measured
______________________________________
1 20.7 23.5 4.6 9.7
20.3 7.1
2 39.2 36.6 12.5 19.6
35.2 12.7
3 24.8 30.1 69.4 71.5
30.2 66.2
4 26.7 25.4 7.0 8.2
26.1 6.1
5 28.0 27.0 57.2 64.1
29.0 64.3
6 28.3 22.5 62.1 63.4
7 43.2 42.9 64.9 61.6
8 27.6 22.7 82.7 82.5
9 35.0 35.9 68.2 72.9
______________________________________
It can also be seen in Table 1 that the amount of titanium present as double phosphates NaTi2 (PP4)3 and Na4 (TiO)(PO4)2 decreases with increasing values of the NaCN to Ti ratios. To confirm that the presence among reaction products of such double phosphates (e.g. reactions 1, 2, 4 and 5) implies not having sufficient NaCN in the system, applicant reacted NaCN with Na4 (TiO)(PO4)2 and with NaTi2 (PO4)3. The results are shown in Table 1, reactions 8 and 9; it can be seen that the conversion of the titanium from the double phosphates into TiN was complete. Examination of the TiN powders with a scanning microscope showed that the powders consist of a mixture of loose submicron particles and larger agglomerates of 30-40 m in their longest axis.
Claims (5)
1. A process for making titanium nitride comprising mixing one or more phosphates of Ti with a cyanide salt in the absence of oxygen and heating for a time sufficient and to a temperature sufficient to cause reaction to occur.
2. The process of claim 1 wherein said cyanide salt is present relative to said phosphates of Ti in a ratio of 2 or greater.
3. The process of claim 2 wherein said time is not less than 24 hours and said temperature is not less than 1000° C.
4. The process of claim 3 wherein said cyanide salt is sodium cyanide.
5. The process of claim 4 wherein said phosphates of Ti are TiP2 O7 and (TiO)2 P2 O7.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/207,806 USH649H (en) | 1988-06-17 | 1988-06-17 | Preparing titanium nitride powder |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/207,806 USH649H (en) | 1988-06-17 | 1988-06-17 | Preparing titanium nitride powder |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH649H true USH649H (en) | 1989-07-04 |
Family
ID=22772074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/207,806 Abandoned USH649H (en) | 1988-06-17 | 1988-06-17 | Preparing titanium nitride powder |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USH649H (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE1006115A5 (en) * | 1992-08-10 | 1994-05-17 | Ministere De La Region Wallonn | Nitride method of preparation. |
-
1988
- 1988-06-17 US US07/207,806 patent/USH649H/en not_active Abandoned
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE1006115A5 (en) * | 1992-08-10 | 1994-05-17 | Ministere De La Region Wallonn | Nitride method of preparation. |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: UNITED STATES OF AMERICA, THE, AS REPRESENTED BY T Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:BAMBERGER, CARLOS E.;REEL/FRAME:004982/0562 Effective date: 19880610 |
|
| STCF | Information on status: patent grant |
Free format text: PATENTED CASE |