US2694653A - Production of metallic titanium - Google Patents
Production of metallic titanium Download PDFInfo
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- US2694653A US2694653A US20596A US2059648A US2694653A US 2694653 A US2694653 A US 2694653A US 20596 A US20596 A US 20596A US 2059648 A US2059648 A US 2059648A US 2694653 A US2694653 A US 2694653A
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- titanium
- tetraiodide
- iodine
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- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 title claims description 60
- 239000010936 titanium Substances 0.000 title claims description 60
- 229910052719 titanium Inorganic materials 0.000 title claims description 60
- 238000004519 manufacturing process Methods 0.000 title description 4
- NLLZTRMHNHVXJJ-UHFFFAOYSA-J titanium tetraiodide Chemical compound I[Ti](I)(I)I NLLZTRMHNHVXJJ-UHFFFAOYSA-J 0.000 claims description 60
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 54
- 239000011630 iodine Substances 0.000 claims description 41
- 229910052740 iodine Inorganic materials 0.000 claims description 41
- 239000004408 titanium dioxide Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 17
- 239000000463 material Substances 0.000 claims description 12
- 238000010494 dissociation reaction Methods 0.000 claims description 11
- 230000005593 dissociations Effects 0.000 claims description 10
- 230000009471 action Effects 0.000 claims description 9
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 8
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 37
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 26
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 12
- 229910052799 carbon Inorganic materials 0.000 description 10
- 230000009467 reduction Effects 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 230000008569 process Effects 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 239000003638 chemical reducing agent Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 3
- 150000004694 iodide salts Chemical class 0.000 description 3
- QPBYLOWPSRZOFX-UHFFFAOYSA-J tin(iv) iodide Chemical class I[Sn](I)(I)I QPBYLOWPSRZOFX-UHFFFAOYSA-J 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 239000003610 charcoal Substances 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004508 fractional distillation Methods 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002006 petroleum coke Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- -1 Hastelloy B Chemical compound 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 229910000990 Ni alloy Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- IAYXVNDWLLVXOK-UHFFFAOYSA-N [Ti].[I] Chemical compound [Ti].[I] IAYXVNDWLLVXOK-UHFFFAOYSA-N 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 208000018459 dissociative disease Diseases 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- YDZQQRWRVYGNER-UHFFFAOYSA-N iron;titanium;trihydrate Chemical compound O.O.O.[Ti].[Fe] YDZQQRWRVYGNER-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- JHGCXUUFRJCMON-UHFFFAOYSA-J silicon(4+);tetraiodide Chemical compound [Si+4].[I-].[I-].[I-].[I-] JHGCXUUFRJCMON-UHFFFAOYSA-J 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910001773 titanium mineral Inorganic materials 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B34/00—Obtaining refractory metals
- C22B34/10—Obtaining titanium, zirconium or hafnium
- C22B34/12—Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08
- C22B34/129—Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08 obtaining metallic titanium from titanium compounds by dissociation, e.g. thermic dissociation of titanium tetraiodide, or by electrolysis or with the use of an electric arc
Definitions
- This invention relates to the production of metallic titanium and has for an object the provision of an improved method or process for producing high-purity metallic titanium. More particularly, the invention contemplates the provision of an improved method or process for producing high-purity metallic titanium by dissociation of titanium tetraiodide.
- titanium-bearing ore is subjected to a suitable treatment to recover all or a large proportion of the titanium in the form of pure titanium dioxide.
- the conversion of the ore to pure titanium dioxide may be carried out in any suitable manner as, for example, by the sulphuric acid-hydrolysis process commonly employed for producing titanium dioxide from ilmenite in the pig ment industry. If titanium dioxide of suitable purity is available at commercially economical prices or if natural titanium dioxide can be obtained at a price sufficiently low to offset the increased cost of operation due to the presence of impurities, this step may be omitted from the complete process of the invention.
- the titanium dioxide available or produced is subjected to a suitable treatment which will convert the titanium to a form in which it is capable of reacting with iodine to produce titanium tetraiodide.
- the titanium of the titanium dioxide may be converted into such a suitable form by reduction to the metallic state. Reduction of the titanium of the titanium dioxide may be carried out by means of either non-carbonaceous reducing agents such as sodium, calcium, magnesium, silicon and aluminum or carbonaceous reducing agents such as charcoal and petroleum coke.
- the metallic titanium produced by reduction of the titanium dioxide with a non-carbonaceous reducing agent can be used for producing titanium tetraiodide. I have found, however, that reduction with an excess of carbon produces a product which provides a better reaction material and which is less expensive than the product resulting from reduction by means of non-carbonaceous reducing agents.
- titanium carbide I prefer to reduce the titanium of the titanium dioxide with carbon in amount sufiicient to produce titanium carbide, as l have found iodine will react with titanium clmgbidec rapidly and efiiciently at a temperature near Titanium carbide can be produced by heating a mixture of titanium dioxide and carbon to a temperature of about 1050 C. at atmospheric pressures, but the reaction is slow and can be made to go to completion only with difficulty. incomplete y reduced material does not react readily with iodine. Therefore, I prefer to carry out the reduction with carbon at a higher temperature. I have found that a highly reactive titanium carbide product may be obtained by carrying out the reduction at temperatures in the range 1300 C. to 1800 C.
- ti tanium carbide formed at 1300" C. under vacuum may be as much as ten percent more reactive than titanium carbide formed at 1800 C. under atmospheric pressure.
- the advantage of greater reactivity may be offset to some iceextent by the cost and inconvenience of operating under a vacuum.
- An electric resistance furnace of the type employed in producing silicon carbide may be employed advantageously in carrying out the reduction of titanium with carbon to produce titanium carbide.
- the titanium carbide produced is subjected to the action of iodine vapor at an elevated temperature. I have found that the rate of reaction reaches a maximum at 1100" C. and falls off at lower and higher temperatures.
- the titanium tetraiodide produced is subjected to a fractionation treatment to separate pure titanium tetraiodide from such contaminants as iodine and iodides of elements other than titanium which may be present in the gaseous product of the reaction between the iodine and the titanium carbide product.
- a fractionation treatment to separate pure titanium tetraiodide from such contaminants as iodine and iodides of elements other than titanium which may be present in the gaseous product of the reaction between the iodine and the titanium carbide product.
- No difficulty is encountered in fractionating the product and producing pure titanium tetraiodide, as, in general, the boiling points of the iodides of the metals which are likely to be present in the titanium carbide as impurities are very much higher than that of titanium tetraiodide. Silicon and tin tetraiodides are exceptions to this rule.
- the boiling point of silicon tetraiodide is 287 C., almost below that of titanium tetraiodide, and, therefore, its presence should not complicate the fractionating operation.
- Tin tetraiodide has almost the same boiling point as titanium tetraiodide, but this element is not likely to be present in any appreciable quantity in titanium ore, so no difiiculty should be encountered.
- One of the more important functions of the fractionating step is to effect the removal of iodides of elements other than titanium which may be present in the gaseous product resulting from treatment of the titanium carbide with iodine.
- Another important function of the fractionating step will be to eifect the separation of unreacted or unconsumed elemental iodine. Separation of iodine from titanium tetraiodide presents no particularly difiicult problem as the two materials have substantially different boiling points, that of iodine being 183 C. and that of titanium tetraiodide being 379 C.
- Fractionation may be carried out by means of controlled cooling of the gaseous product of the iodine-titanium carbide reaction, or the gaseous product may be cooled and condensed, and the components of the condensate may be separated by fractional distillation.
- Fractional distillation preferably is carried out at temperatures between the melting point and the boilin point of titanium tetraiodide, in the range C. to 379 C., under reduced pressures, that is, under pressures lower than atmospheric pressures. Any suitable pressure which will permit attainment of the results sought may be employed.
- the gaseous product resulting from treatment of titanium-bearing material with iodine contains only titanium tetraiodide and one or more substances like iodine having boiling points lower than that of titanium tetraiodide, the product may be cooled and condensed, and a pure titanium tetraiodide product may be obtained as a residue resulting from distillation of the condensate.
- a gaseous product consisting essentially of titanium tetraiodide is passed in contact with a surface heated to and maintained at a temperature in the range 1100 C. to 1700 C.
- Contact of the titanium tetraiodide with the heated surface results in dissociation of the titanium tetraiodide into titanium and gaseous elemental iodine and deposition of metallic titanium of high purity.
- the deposition surface may be formed of tungsten or titanium or other suitable material, and it may be heated in any suitable manner.
- the gaseous elemental iodine produced is utilized in the process for treating additional titanium-bearing materials for the production of titanium tetraiodide.
- the elemental iodine produced by the dissociation reaction may be used directly in the vapor state or after condensation to the liquid or solid state for treating additional titanium-bearing material.
- the method of recovering high-purity metallic titanium from titanium-bearing ore which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment to produce a relatively crude metallic titanium-bearing product capable of reacting with iodine to produce a titanium tetraiodide product, subjecting the crude metallic titanium-bearing product to the action of iodine to produce a titanium tetraiodide-containing product, subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment to produce substantially pure metallic titanium and elemental iodine by passing the titanium tetraiodide in vapor form in contact with a body of metallic titanium heated to a temperature in the range, 1100 C. to 1700 C., and utilizing the iodine in the treatment of additional crude metallic titanium-bea
- the method of recovering high-purity metallic titanium from titanium-bearing ore which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine to form a titanium tetraiodidecontaining product, subjecting the titanium tetraiodidecontaining product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment to produce substantially pure metallic titanium and elemental iodine by passing the titanium tetraiodide in vapor form in contact with a body of metallic titanium heated to a temperature in the range, 1lOO C. to 1700 C., and utilizing the iodine in the treatment of additional titanium carbide.
- the method of recovering high-purity metallic titanium from titanium-bearing ore which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine to form a titanium tetraiodide-containing product, subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment by passing the titanium tetraiodide in contact with a refractory surface comprising metallic titanium maintained at a temperature in the range 1100 C. to 1700 C. to produce substantially pure metallic titanium and elemental iodine, and utilizing the iodine in the treatment of additional titanium carbide.
- the method of recovering high-purity metallic titanium from titanium-bearing are which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine in vapor form at an elevated temperature near 1100 C.
- titanium tetraiodide-containing product subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment to produce substantially pure metallic titanium and elemental iodine by passing the titanium tetraiodide in vapor form in contact with a body of metallic titanium heated to a temperature in the range, 1100 C. to 1700 C., and utilizing the iodine in the treatment of additional titanium carbide.
- the method of recovering high-purity metallic titanium from titanium-bearing ore which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine in vapor form at an elevated temperature near 1100 C. to form a titanium tetraiodide-containing product subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment by passing the titanium tetraiodide in contact with a refractory surface comprising metallic titanium maintained at a temperature in the range 1100 C. to 1700 C. to produce substantially pure metallic titanium and elemental iodine, and utilizing the iodine in the treatment of additional titanium carbide.
- the method of recovering high-purity metallic titanium from titanium dioxide which comprises subjecting the titanium dioxide to a reducing treatment to produce a relatively crude metallic titanium-bearing product capable of reacting with iodine to produce a titanium tetraiodide product, subjecting the crude metallic titanium-bearing product to the action of iodine to produce a titanium tetraiodide-containing product, subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment by passing the titanium tetraiodide in contact with a refractory surface maintained at a temperature in the range 1100 C. to 1700 C. to produce substantially pure metallic titanium and elemental iodine, and utilizing the iodine in the treatment of additional crude metallic titanium-bearing material.
- the method of recovering high-purity metallic titanium from titanium dioxide which comprises subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine in vapor form at an elevated temperature near 1100 C. to form a titanium tetraiodide-containing product, subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment by passing the titanium tetraiodide in contact with a refractory surface maintained at a temperature in the range 1100" C. to 1700 C. to produce substantially pure metallic titanium and elemental iodine, and utilizing the iodine in the treatment of additional titanium carbide.
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- General Life Sciences & Earth Sciences (AREA)
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Description
United States Patent PRODUCTION OF METALLIC TITANIUM Alfred C. Loonam, New York, N. Y., assignor to Chilean Nitrate Sales Corporation, New York, N. Y., a corporation of New York No Drawing. Application April 12, 1948, Serial No. 20,596
7 Claims. (Cl. 117-107) This invention relates to the production of metallic titanium and has for an object the provision of an improved method or process for producing high-purity metallic titanium. More particularly, the invention contemplates the provision of an improved method or process for producing high-purity metallic titanium by dissociation of titanium tetraiodide.
The term ore as employed in the specification and claims is intended to include concentrates and other titanium mineral-bearing materials as well as natural ore.
In accordance with the invention, titanium-bearing ore is subjected to a suitable treatment to recover all or a large proportion of the titanium in the form of pure titanium dioxide.
The conversion of the ore to pure titanium dioxide may be carried out in any suitable manner as, for example, by the sulphuric acid-hydrolysis process commonly employed for producing titanium dioxide from ilmenite in the pig ment industry. If titanium dioxide of suitable purity is available at commercially economical prices or if natural titanium dioxide can be obtained at a price sufficiently low to offset the increased cost of operation due to the presence of impurities, this step may be omitted from the complete process of the invention.
The titanium dioxide available or produced is subjected to a suitable treatment which will convert the titanium to a form in which it is capable of reacting with iodine to produce titanium tetraiodide. The titanium of the titanium dioxide may be converted into such a suitable form by reduction to the metallic state. Reduction of the titanium of the titanium dioxide may be carried out by means of either non-carbonaceous reducing agents such as sodium, calcium, magnesium, silicon and aluminum or carbonaceous reducing agents such as charcoal and petroleum coke.
The metallic titanium produced by reduction of the titanium dioxide with a non-carbonaceous reducing agent can be used for producing titanium tetraiodide. I have found, however, that reduction with an excess of carbon produces a product which provides a better reaction material and which is less expensive than the product resulting from reduction by means of non-carbonaceous reducing agents.
I prefer to reduce the titanium of the titanium dioxide with carbon in amount sufiicient to produce titanium carbide, as l have found iodine will react with titanium clmgbidec rapidly and efiiciently at a temperature near Titanium carbide can be produced by heating a mixture of titanium dioxide and carbon to a temperature of about 1050 C. at atmospheric pressures, but the reaction is slow and can be made to go to completion only with difficulty. incomplete y reduced material does not react readily with iodine. Therefore, I prefer to carry out the reduction with carbon at a higher temperature. I have found that a highly reactive titanium carbide product may be obtained by carrying out the reduction at temperatures in the range 1300 C. to 1800 C. At temperatures in the lower portion of the range, I prefer to effect the heating and reduction under a vacuum. Products formed at the lower temperatures under reduced pressures are more highly reactive than products formed at higher temperatures under atmospheric pressure. Thus. for example, ti tanium carbide formed at 1300" C. under vacuum may be as much as ten percent more reactive than titanium carbide formed at 1800 C. under atmospheric pressure. The advantage of greater reactivity may be offset to some iceextent by the cost and inconvenience of operating under a vacuum. Normally, I prefer to operate under atmospheric pressure at a high temperature in the neighborhood of 1800" C. in view of the large quantities of gas produced in the reaction. An electric resistance furnace of the type employed in producing silicon carbide may be employed advantageously in carrying out the reduction of titanium with carbon to produce titanium carbide.
In order to limit contamination of the titanium carbide, I prefer to employ petroleum coke or charcoal as the reducing agent.
The titanium carbide produced is subjected to the action of iodine vapor at an elevated temperature. I have found that the rate of reaction reaches a maximum at 1100" C. and falls off at lower and higher temperatures.
In carrying out the reaction between iodine and titanium carbide at the higher temperatures, I prefer to employ a furnace lined with graphite, as the results of my investigations indicate that graphite is not attacked at any temperature by iodine vapor. I prefer, also, to employ electrical resistance heating because of ease of control, etficiency and the absence of any gaseous products of com bustion which, if present, might contaminate the titanium tetraiodide produced.
The titanium tetraiodide produced is subjected to a fractionation treatment to separate pure titanium tetraiodide from such contaminants as iodine and iodides of elements other than titanium which may be present in the gaseous product of the reaction between the iodine and the titanium carbide product. No difficulty is encountered in fractionating the product and producing pure titanium tetraiodide, as, in general, the boiling points of the iodides of the metals which are likely to be present in the titanium carbide as impurities are very much higher than that of titanium tetraiodide. Silicon and tin tetraiodides are exceptions to this rule. The boiling point of silicon tetraiodide is 287 C., almost below that of titanium tetraiodide, and, therefore, its presence should not complicate the fractionating operation. Tin tetraiodide has almost the same boiling point as titanium tetraiodide, but this element is not likely to be present in any appreciable quantity in titanium ore, so no difiiculty should be encountered.
One of the more important functions of the fractionating step is to effect the removal of iodides of elements other than titanium which may be present in the gaseous product resulting from treatment of the titanium carbide with iodine.
Another important function of the fractionating step will be to eifect the separation of unreacted or unconsumed elemental iodine. Separation of iodine from titanium tetraiodide presents no particularly difiicult problem as the two materials have substantially different boiling points, that of iodine being 183 C. and that of titanium tetraiodide being 379 C.
Fractionation may be carried out by means of controlled cooling of the gaseous product of the iodine-titanium carbide reaction, or the gaseous product may be cooled and condensed, and the components of the condensate may be separated by fractional distillation.
Fractional distillation preferably is carried out at temperatures between the melting point and the boilin point of titanium tetraiodide, in the range C. to 379 C., under reduced pressures, that is, under pressures lower than atmospheric pressures. Any suitable pressure which will permit attainment of the results sought may be employed.
When the gaseous product resulting from treatment of titanium-bearing material with iodine contains only titanium tetraiodide and one or more substances like iodine having boiling points lower than that of titanium tetraiodide, the product may be cooled and condensed, and a pure titanium tetraiodide product may be obtained as a residue resulting from distillation of the condensate.
For the fractionating operation and other operations in which liquid or gaseous iodine or titanium tetraiodide are handled, I prefer to employ apparatus comprising nickel and nickel alloys such as Hastelloy B, although any suitable materials may be employed.
According to a method or process of the invention, a gaseous product consisting essentially of titanium tetraiodide is passed in contact with a surface heated to and maintained at a temperature in the range 1100 C. to 1700 C. Contact of the titanium tetraiodide with the heated surface results in dissociation of the titanium tetraiodide into titanium and gaseous elemental iodine and deposition of metallic titanium of high purity. The deposition surface may be formed of tungsten or titanium or other suitable material, and it may be heated in any suitable manner.
The gaseous elemental iodine produced is utilized in the process for treating additional titanium-bearing materials for the production of titanium tetraiodide. The elemental iodine produced by the dissociation reaction may be used directly in the vapor state or after condensation to the liquid or solid state for treating additional titanium-bearing material.
I claim:
1. The method of recovering high-purity metallic titanium from titanium-bearing ore which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment to produce a relatively crude metallic titanium-bearing product capable of reacting with iodine to produce a titanium tetraiodide product, subjecting the crude metallic titanium-bearing product to the action of iodine to produce a titanium tetraiodide-containing product, subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment to produce substantially pure metallic titanium and elemental iodine by passing the titanium tetraiodide in vapor form in contact with a body of metallic titanium heated to a temperature in the range, 1100 C. to 1700 C., and utilizing the iodine in the treatment of additional crude metallic titanium-bearing material.
2. The method of recovering high-purity metallic titanium from titanium-bearing ore which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine to form a titanium tetraiodidecontaining product, subjecting the titanium tetraiodidecontaining product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment to produce substantially pure metallic titanium and elemental iodine by passing the titanium tetraiodide in vapor form in contact with a body of metallic titanium heated to a temperature in the range, 1lOO C. to 1700 C., and utilizing the iodine in the treatment of additional titanium carbide.
3. The method of recovering high-purity metallic titanium from titanium-bearing ore which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine to form a titanium tetraiodide-containing product, subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment by passing the titanium tetraiodide in contact with a refractory surface comprising metallic titanium maintained at a temperature in the range 1100 C. to 1700 C. to produce substantially pure metallic titanium and elemental iodine, and utilizing the iodine in the treatment of additional titanium carbide.
4. The method of recovering high-purity metallic titanium from titanium-bearing are which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine in vapor form at an elevated temperature near 1100 C. to form a titanium tetraiodide-containing product, subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment to produce substantially pure metallic titanium and elemental iodine by passing the titanium tetraiodide in vapor form in contact with a body of metallic titanium heated to a temperature in the range, 1100 C. to 1700 C., and utilizing the iodine in the treatment of additional titanium carbide.
5. The method of recovering high-purity metallic titanium from titanium-bearing ore which comprises subjecting the ore to a suitable treatment and producing substantially pure titanium dioxide, subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine in vapor form at an elevated temperature near 1100 C. to form a titanium tetraiodide-containing product subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment by passing the titanium tetraiodide in contact with a refractory surface comprising metallic titanium maintained at a temperature in the range 1100 C. to 1700 C. to produce substantially pure metallic titanium and elemental iodine, and utilizing the iodine in the treatment of additional titanium carbide.
6. The method of recovering high-purity metallic titanium from titanium dioxide which comprises subjecting the titanium dioxide to a reducing treatment to produce a relatively crude metallic titanium-bearing product capable of reacting with iodine to produce a titanium tetraiodide product, subjecting the crude metallic titanium-bearing product to the action of iodine to produce a titanium tetraiodide-containing product, subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment by passing the titanium tetraiodide in contact with a refractory surface maintained at a temperature in the range 1100 C. to 1700 C. to produce substantially pure metallic titanium and elemental iodine, and utilizing the iodine in the treatment of additional crude metallic titanium-bearing material.
7. The method of recovering high-purity metallic titanium from titanium dioxide which comprises subjecting the titanium dioxide to a reducing treatment with carbon to produce titanium carbide, subjecting the titanium carbide to the action of iodine in vapor form at an elevated temperature near 1100 C. to form a titanium tetraiodide-containing product, subjecting the titanium tetraiodide-containing product to a fractionating treatment to separate pure titanium tetraiodide, subjecting the titanium tetraiodide to a dissociation treatment by passing the titanium tetraiodide in contact with a refractory surface maintained at a temperature in the range 1100" C. to 1700 C. to produce substantially pure metallic titanium and elemental iodine, and utilizing the iodine in the treatment of additional titanium carbide.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 1,497,417 Weber June 10, 1924 1,671,213 Van Arkel et al May 29, 1928 1,891,124 Van Arkel et al Dec. 13, 1932 2,237,503 Ridgway Apr. 8, 1941 2,393,264 Rentschler et al Jan. 22, 1946 2,519,385 Loonam Aug. 22, 1950
Claims (1)
1. THE METHOD OF RECOVERING HIGH-PURITY METALLIC TITANIUM FROM TITANIUM-BEARING ORE WHICH COMPRISES SUBJECTING THE ORE TO A SUITABLE TREATMENT AND PRODUCING SUBSTANTIALLY PURE TITANIUM DIOXIDE, SUBJECTING THE TITANIUM DIOXIDE TO A REDUCING TREATMENT TO PRODUCT A RELATIVELY CRUDE METALLIC TITANIUM-BEARING PRODUCT CAPABLE OF REACTING WITH IODINE TO PRODUCE A TITANIUM TETRAIODIDE PROUDCT, SUBJECTING THE CRUDE METALLIC TITANIUM-BEARING PRODUCT TO THE ACTION OF IODINE TO PRODUCE A TITANIUM TETRAIODIDE-CONTAINING PRODUCT, SUBJECTING THE TITANIUM TETRAIODIDE-CONTAINING PRODUCT TO A FRACTIONATING TREATMENT TO SEPARATE PURE TITANIUM TETRAIODIDE, SUBJECTING THE TITANIUM TETRAIODIDE TO A DISSOCIATION TREATMENT TO PRODUCE SUBSTANTIALLY PURE METALLIC TITANIUM AND ELEMENTAL IODINE BY PASSING THE TITANIUM TETRAIODIDE IN VAPOR FORM IN CONTACT WITH A BODY OF METALLIC TITANIUM HEATED TO A TEMPERATURE IN THE RANGE, 1100* C. TO 1700* C., AND UTILIZING THE IODINE IN THE TREATMENT OF ADDITIONAL CRUDE METALLIC TITANIUM-BEARING MATERIAL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20596A US2694653A (en) | 1948-04-12 | 1948-04-12 | Production of metallic titanium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20596A US2694653A (en) | 1948-04-12 | 1948-04-12 | Production of metallic titanium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2694653A true US2694653A (en) | 1954-11-16 |
Family
ID=21799493
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US20596A Expired - Lifetime US2694653A (en) | 1948-04-12 | 1948-04-12 | Production of metallic titanium |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2694653A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2812250A (en) * | 1952-09-29 | 1957-11-05 | Du Pont | Production of titanium by the reduction of titanium tetrachloride by magnesium |
| US2895852A (en) * | 1954-11-16 | 1959-07-21 | Chilean Nitrate Sales Corp | Titanium metallurgy |
| US2982017A (en) * | 1953-05-22 | 1961-05-02 | Union Carbide Corp | Method of protecting magnesium with a coating of titanium |
| US3049440A (en) * | 1959-07-28 | 1962-08-14 | Chilean Nitrate Sales Corp | Process and apparatus for the vapor deposition of metals |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1497417A (en) * | 1919-03-31 | 1924-06-10 | Henry C P Weber | Process of coating metals |
| US1671213A (en) * | 1925-03-14 | 1928-05-29 | Philips Nv | Process of precipitaing metals on an incandescent body |
| US1891124A (en) * | 1928-06-14 | 1932-12-13 | Philips Nv | Process of precipitating metals on an incandescent body |
| US2237503A (en) * | 1937-04-19 | 1941-04-08 | Norton Co | Titanium carbide and a method of making the same |
| US2393264A (en) * | 1942-09-23 | 1946-01-22 | Westinghouse Electric Corp | Photoelectric device and the manufacture thereof |
| US2519385A (en) * | 1948-04-12 | 1950-08-22 | Chilean Nitrate Sales Corp | Production of titanium tetraiodide |
-
1948
- 1948-04-12 US US20596A patent/US2694653A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1497417A (en) * | 1919-03-31 | 1924-06-10 | Henry C P Weber | Process of coating metals |
| US1671213A (en) * | 1925-03-14 | 1928-05-29 | Philips Nv | Process of precipitaing metals on an incandescent body |
| US1891124A (en) * | 1928-06-14 | 1932-12-13 | Philips Nv | Process of precipitating metals on an incandescent body |
| US2237503A (en) * | 1937-04-19 | 1941-04-08 | Norton Co | Titanium carbide and a method of making the same |
| US2393264A (en) * | 1942-09-23 | 1946-01-22 | Westinghouse Electric Corp | Photoelectric device and the manufacture thereof |
| US2519385A (en) * | 1948-04-12 | 1950-08-22 | Chilean Nitrate Sales Corp | Production of titanium tetraiodide |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2812250A (en) * | 1952-09-29 | 1957-11-05 | Du Pont | Production of titanium by the reduction of titanium tetrachloride by magnesium |
| US2982017A (en) * | 1953-05-22 | 1961-05-02 | Union Carbide Corp | Method of protecting magnesium with a coating of titanium |
| US2895852A (en) * | 1954-11-16 | 1959-07-21 | Chilean Nitrate Sales Corp | Titanium metallurgy |
| US3049440A (en) * | 1959-07-28 | 1962-08-14 | Chilean Nitrate Sales Corp | Process and apparatus for the vapor deposition of metals |
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