GB2399815A - Making activated nickel and producing nickel carbonyl therefrom - Google Patents
Making activated nickel and producing nickel carbonyl therefrom Download PDFInfo
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- GB2399815A GB2399815A GB0406594A GB0406594A GB2399815A GB 2399815 A GB2399815 A GB 2399815A GB 0406594 A GB0406594 A GB 0406594A GB 0406594 A GB0406594 A GB 0406594A GB 2399815 A GB2399815 A GB 2399815A
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- nickel
- chloride
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- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 title claims abstract description 233
- 229910052759 nickel Inorganic materials 0.000 title claims abstract description 67
- 150000002815 nickel Chemical class 0.000 title claims description 9
- 238000000034 method Methods 0.000 claims abstract description 53
- 230000008569 process Effects 0.000 claims abstract description 49
- 238000000354 decomposition reaction Methods 0.000 claims abstract description 27
- 238000004519 manufacturing process Methods 0.000 claims abstract description 23
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims abstract description 19
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 18
- 239000001257 hydrogen Substances 0.000 claims abstract description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 16
- 150000002816 nickel compounds Chemical class 0.000 claims abstract description 16
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims abstract description 13
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 claims abstract description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 claims abstract description 12
- 229910000008 nickel(II) carbonate Inorganic materials 0.000 claims abstract description 11
- ZULUUIKRFGGGTL-UHFFFAOYSA-L nickel(ii) carbonate Chemical compound [Ni+2].[O-]C([O-])=O ZULUUIKRFGGGTL-UHFFFAOYSA-L 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 10
- 239000002243 precursor Substances 0.000 claims abstract description 7
- 238000011065 in-situ storage Methods 0.000 claims abstract description 4
- 238000006243 chemical reaction Methods 0.000 claims description 23
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical group ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- 230000008021 deposition Effects 0.000 claims description 6
- 239000000758 substrate Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims 1
- 229910001617 alkaline earth metal chloride Inorganic materials 0.000 claims 1
- 229910000480 nickel oxide Inorganic materials 0.000 claims 1
- BFDHFSHZJLFAMC-UHFFFAOYSA-L nickel(ii) hydroxide Chemical compound [OH-].[OH-].[Ni+2] BFDHFSHZJLFAMC-UHFFFAOYSA-L 0.000 claims 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 claims 1
- 229910021381 transition metal chloride Inorganic materials 0.000 claims 1
- 238000003860 storage Methods 0.000 abstract description 8
- 238000005137 deposition process Methods 0.000 abstract description 5
- 229910052721 tungsten Inorganic materials 0.000 abstract description 2
- 239000007789 gas Substances 0.000 description 10
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical group [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 239000000843 powder Substances 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- -1 NICKEL CARBONYL Chemical class 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 230000006315 carbonylation Effects 0.000 description 2
- 238000005810 carbonylation reaction Methods 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical class OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910001510 metal chloride Inorganic materials 0.000 description 1
- 229910021508 nickel(II) hydroxide Inorganic materials 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G53/00—Compounds of nickel
- C01G53/02—Carbonyls
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/16—Making metallic powder or suspensions thereof using chemical processes
- B22F9/18—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds
- B22F9/28—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from gaseous metal compounds
-
- 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
- C22B23/00—Obtaining nickel or cobalt
- C22B23/02—Obtaining nickel or cobalt by dry processes
-
- 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
- C22B23/00—Obtaining nickel or cobalt
- C22B23/06—Refining
- C22B23/065—Refining carbonyl methods
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Manufacturing & Machinery (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Catalysts (AREA)
- Carbon And Carbon Compounds (AREA)
Abstract
A process for producing Ni(CO)4 from carbon monoxide and a source of nickel selected from elemental nickel, a nickel compound or mixtures thereof, provided the nickel compound is not nickel chloride per se or in admixture with a nickel carbonate ore, in an amount greater than 50% W/W nickel chloride; which process comprises (a) treating the nickel source with hydrogen at a pressure of at least atmospheric pressure and an effective temperature, in the presence of chloride anion or an in situ generator thereof precursor, to produce a resultant active nickel; (b) reacting the carbon monoxide with the resultant active nickel to produce the Ni(CO)4; and collecting the Ni(CO)4. The process offers the production of Ni(CO)4 at atmospheric pressure and at a sufficiently high rate for direct use in subsequent deposition processes without the need for storage facilities. Apparatus for the decomposition of the Ni(CO)4 so produced is also disclosed.
Description
PROCESS FOR PRODUCING NICKEL CARBONYL,
NICKEL POWDER AND USE THEREOF
FOLD OF THE INVENTION
This invention relates to processes for producing nickel carbonyl, more particularly to producing nickel powders of use in producing said nickel carbonyl by reaction with carbon monoxide, and to said nickel powders made by said process.
BACKGROUND TO TED INVENTION
Nickel carbonyl, Ni(CO)4 was first produced by the reaction of metallic nickel with carbon monoxide by Mond in the early part of the 19 century. Today, one of the major industrial processes for making metallic nickel is based on the production of Ni(C0)4 and subsequent thermal decomposition thereof to Ni and CO. One known commercial process operates at about 1 80 C and a CO pressure of about 70 atm. It is known that the CO pressure may be reduced when the reactant nickel is catalytically activated.
Activation of the metal has been observed in the presence of mercury (1, 2), sulfur in the form of HIS (3, 4), hydrogen (5, 6) or carbon (7). It has been suggested -that 'tale high initial r-ue of formla-ion of Ni(C0)4 and he subsequent decline to z steady state value is the result of a rapid decrease in the number of activated reaction sites which are produced upon heat treatment of the sample (8, 9, 6). A study of surface changes during carbonyl synthesis suggests that the maximum rate is associated with fundamental changes in the defect structure. All of the above methods use catalytic activation of nickel in the presence of CO.
However, it can be readily appreciated that processes that at atmospheric pressure can produce nickel, particularly, activated nickel for subsequent reaction with CO at atmospheric pressure would provide significant capital and operating cost advantages.
Further, it can also be appreciated that processes that enable Ni(CO)4 to be manufactured at a sufficient rate as to obviate the need for storage in order to build up À . . ' . . . ! . . a sufficient supply for practical, efficient use in a subsequent nickel deposition process, would also offer significant capital and operating cost savings. To-date, in commercial operations rate limitations on the production of Ni(C0)4 require such storage facilities and operations.
There is, thus, a desire for an improved method of Ni(C0)4 production which is operable at atmospheric pressure and which is of a sufficient rate as to negate the need for storage of the Ni(C0)4 prior to use in a subsequent decomposition and/or deposition process.
PUBLICATIONS
1. Morton J.R., Preston K. F. Chem. Phys., 81, 56, (1984).
2. Morton J.K., Preston A. r. snore Cnem., 4, ;;i7, i98;j.
3. MercerD. L., Inco Ltd. (Can. 1038169 [1975/78]).
4. Schafer H. Z Anorg. Ally Chem. 493, 17 (1982).
5. Job R. Chem. MUG 56, 556 (1979).
6. Mazurek H., Mehta R. S., Dresselhaus M. S., Dresselhaus G., Zeiger H. J. SuSci. 118, 530 (1982).
7. Korenev A. Vet, Shvartsman R. A., Mnukbin A. S., Tsvetn Met. 1979 Not 1, pp.37.
8. Mehta R. S., Dresselhaus M. S., Dresselhaus G., Zeiger H. J. SO Sci. 78, L681 (1978).
9. Greiner G., Manzel D. Catal. 77 382 (1982).
SUGARY OF THE INVENTION
It is an object of the present invention to provide a process for the commercial À production of Ni(COh from a source of nickel in an efficacious manner at atmospheric pressure, with resultant capital and operating cost savings.
It is a further object of the present invention to provide a process and apparatus for the commercial continuous production of Ni(C0)4 from a source of nickel at a sufficiently high rate as to negate the need for storage of the Ni(COh prior to a subsequent decomposition step, with resultant capital and operating cost savings. t.
t À t.:. ; .
Accordingly, in one aspect the invention provides a process for producing Ni(CO)4 from carbon monoxide and a source of nickel selected from the group consisting of elemental nickel, a nickel compound or mixtures thereof, provided said nickel compound is not nickel chloride Mar se or in admixture with a nickel carbonate ore in an amount greater than 50% w/w nickel chloride which process comprises (a) treating said nickel source with hydrogen at a pressure of at least atmospheric pressure and an effective temperature, in the presence of chloride anion or an in situ generator thereof precursor; to produce a resultant active nickel, and (b) reacting said carbon monoxide with said resultant active nickel to produce said Ni(CO)4.
By the term "resultant active nickel" as used in this specification and claims is meant resultant particulate nickel that reacts with CO at essentially atmospheric pressure and a temperature of from ambient (20 C) to 80 C to effect conversion to Ni(C0)4 at an acceptable conversion rate.
By the term "acceptable conversion rate" is meant herein the rate of production of Ni(C0)4 in the order of at least 0.1 g/hr Ni(C0)4 per g/Ni, which provides an efficacious rate for direct utilization, without the need for a build-up in storage, preferably for use in a commercial subsequent deposition process. A more acceptable rate is 1 g/hr Ni(C0)4 per glNi and a still more advantageous rate is the maximum rate of 3.0 g/hr. Ni(CO)4 per glNi.
The effective temperature is a temperature which effects the production of resultant active nickel at an acceptable rate of at least atmospheric pressure.
Preferably, the effective temperature is in the range 300 - 650 C and more pre.=erly, 350 - 550 C.
The Ni(CO)4 produced in step (b) may be collected, or, alternatively, when made at an acceptable conversion rate, as herein defined, preferably of at least 0.25 g/hr Ni(C0)4 per g Ni, preferably, at a rate of 3.0 g/hr Ni(CO)4 per g Ni directly passed to a deposition chamber for immediate decomposition to Ni and CO. This enables the CO to be immediately recycled in a closed-loop manner as to provide a continuous CO closed- loop process.
Accordingly, in a further aspect, the invention provides an improved apparatus for the production of nickel powder, coatings, articles or compounds from the decomposition of Ni(C0)4, said apparatus comprising: , , : . i : . . (a) a decomposition chamber having a Ni(CO)4 feed inlet. a spent CO outlet and adapted to receive a substrate, (b) a Ni(C0)4 production chamber having a CO feed inlet, a gaseous Ni(CO) 4 product outlet and adapted to receive source nickel for reaction with CO, wherein the improved apparatus comprises (i) Ni(CO)4 direct feed means between said Ni(C0)4 reed inlet of said decomposition chamber for feeding Ni(C0)4 directly from said production chamber to said decomposition chamber at an acceptable feed rate: (ii) CO recycle conduit means between said spent CO outlet and said CO feed inlet; and (iii)wherein said source nickel comprises activated nickel produced as hereinabove defined.
Present prior art processes have very low conversion rates, typically of less than 0.03 g Ni(C0)4 /fur. per g/Ni, which requires that the Ni(C0)4 needs to be stored to a required volume prior to use in a subsequent decomposition or deposition step.
The nickel compounds of use in the practice of the invention as hereinabove defined may readily be selected, from, but not limited to, for example, the group consisting of a nickel salt, most particularly, nickel chloride, carbonate, hydroxide, oxide and metallic elemental nickel. The metallic elemental nickel is most preferably in particulate form, for example, as a very fine powder.
1 ne preferred nickel salt is nickel chloride, preferably in She forms of a hydrae, or a mixture thereof with nickel carbonate in the form of zaratite (2Ni(OH)2 NiCO3.4H2O), preferably wherein the amount of nickel chloride is such as to produce 20 - 25% W/W of chloride based on nickel in the mixture.
The chloride anion may be selected from, by way of example, but not limited to, hydrogen chloride and a metallic chloride salt, such as, for example, an alkali, alkaline earth or transition metal simple or complex salt, e.g. FeCI3. The invention also includes processes that involve the use of precursors of chloride ion under the reaction conditions defined, such as, for example, suitable use of Cl2, oxides of chlorine gas and OC13 salts that produce chloride anion m situ.
The chloride anion is, preferably, present at a ratio of at least 1:10 atomic W/W% Cl to Ni, more preferably 1:5 atomic W/W%. .
L r L. : . , . ..
: . ; A preferred process is wherein the chloride anion is present as gaseous hydrochloric acid in gaseous admixture with the hydrogen, and more preferably, wherein the nickel compound is first treated with hydrogen at the effective temperature for a first period of time and subsequently treated with the gaseous admixture for a second period of time, at the effective temperature.
The chloride anion in alternative embodiments may be generated m situ under the aforesaid process conditions, according to the invention as defined, in requisite effective amounts from chloride anion generating precursors, such as, for example, chlorate compounds and chlorine gas.
In a further aspect, the invention provides the resultant active nickel when made by a process as hereinabove defined prior to its subsequent reaction with GO to form Ni(CO)4.
In a yet further aspect, the invention provides a process as hereinabove defined for producing resultant nickel from the decomposition of nickel carbonyl produced by a process as hereinabove defined.
We have found, fiercer, that relatively small amounts of metal chlorides, e.g. ferric chloride in the presence of non-chloride nickel compounds enable activated nickel to be formed according to the process ofthe invention as hereinabove defined.
The gaseous product stream comprises H2 and HCI and, optionally, H2O, CO2 and CO.
BREF DESCRIPTION OF 1 DRAWINGS
In order that the invention may be better understood, preferred embodiments will now be described by way of example only with reference to the accompanying drawing, wherein:- Fig. 1 is a graph showing overall conversion ( /0) against reaction time (hr.) for various processes according to the invention, Fig. 2 is a diagrammatic flow diagram of a continuous self-contained process according to the invention, and Fig. 3 is a diagrammatic sketch of a Ni(C0)4 production reaction chamber in direct communication with a Ni deposition chamber according to the invention. . c. .
L
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
In order that the invention may be better understood, preferred embodiments will now be described by way of example only, wherein Examples I and 2 do not constitute part of the invention as claimed but are provided for comparison purposes only.
Example I (Prior Art)
NiCO3 powder (200 g) was placed in an extraction reactor and treated with a stream of H2 gas at 300 mL/min flow rate, at 500 C for 7 hou. s to effect substantially complete reduction. The nickel powder produced was cooled to 100 C and the atmosphere of H2 was subsequently replaced with carbon monoxide. The reactor was cooled further to 50 C and CO gas passed through at 300 mL/min flow rate. The resulting Ni(C0)4 was passed through a pair of carbonyl decomposers according to the prior art and nickel was recovered as nickel powder, (10 g, 10 % yield) after 12 hours.
Example 2 (Prior Art)
Ni(OH)2 powder (100 g) was placed in the extraction reactor and treated with a stream of H2 gas at 300 mLlmin flow, at 500 C for 7 hours to essentially complete reduction. The resulting nickel powder was cooled to 100 C in the atmosphere of Ha which was subsequently replaced with carbon monoxide. The reactor was cooled down furler to 50 C and CO gas passed through at 300 mL/min flow rate. The resulting Ni(C0)4 gas was passed through carbonyl decomposers and nickel powder (fig, 9.5 yield) after 12 hours was recovered.
Example 3
300.1g of a nickel carbonate! nickel chloride mixture (10:1 w/w) was placed into an extraction reactor and treated with hydrogen (2L/min) at 450 C for 6 hours.
Subsequently, the hydrogen was replaced with argon, the reactor cooled to 40 C and the argon replaced with carbon monoxide at a gas temperature of 80 C, and flow rate of 4 L/min. whereby nickel carbonyl was formed, collected and subsequently decomposed to Ni and CO to provide (103g, 70%) yield of nickel extraction yield in 6 hr.
Example 4
302.3 g of the same mixture as in Example 3 was treated under similar conditions but wherein after 0.5 h, the hydrogen gas was doped with 1% of HCI for a further reaction period of 4 hours. The subsequent nickel extraction procedure was similar to Example 3 and gave 134g; 90% yield of nickel in 6 h.
Example 5
300.1 g of nickel carbonate was treated under similar conditions as in Example 4 but wherein after 0.5 h a flow of 900cc/min of HCI gas was introduced into the hydrogen flow at 2 L/min for 4 h. The subsequent nickel extraction procedure was similar to Example 3 and gave a 96.48 % yield of nickel in 13 h. The aforesaid examples 3-5 are better illustrated with reference to Fig. 1 wherein: Line 1 represents the carbonylation of nickel produced by the reaction of a mixture of nickel carbonate/nickel chloride 10:1. (6 h, 70.4% yield) according to Example 3.
Line 2 represents the same composition according to line 1 plus 1% pfHC1 in the gas stream (6 hours, 90.45% yield) according to Example 4; and Line 3 represents 100% nickel carbonate plus HC1 (13 h, 96.48%) according to
Example 5.
The aforesaid examples clearly illustrate the beneficial effect of having chloride anion present in admixture with a nickel compound in the hydrogen reactor in producing a particulate nickel more efficacious in reacting win CO to produce Ni(CO)4
TABLE 1
Example Ni Compound Equivalent Deposited Time Rate** Rate*** (g) Ni(g) Ni(g) (hr)* gNi/gNi/hr Ni(C0)4 (approx.) /gNir #1 200 (NiCO3) 98 10 12 0.01 0.3 #2 100 (Ni(OH2)) 63 6 12 0.01 #3 300 NiCO3 / 147 103 6 0.12 0.36 Ni Cl2 (10:1) #4 302 NiCO3 / 148 134 6 0.15 0.45 Ni Cl2 (10:1) #5 300 g NiCO3 148 142 13 0.07 0.21 ; . . À: c À . . * carbonylation and subsequent decomposition time from treated (reduced) Ni.
** rate of deposition of Ni metal se per hour per 1 gm equivalent Ni, calculated from Ni compound starting material.
*** Rate of production of Ni(CO)4 per hr. per g Ni.
Table 1 shows the beneficial enhancement in the rate of production of Ni from its various sources by the process according to the present invention, wherein the presence of chloride anion in Examples 3, 4 and 5 shows the very significant beneficial effect over the absence of chloride anion in Examples l and 2.
This enhancement in production rate of Ni(C0)4 enables the direct use thereof in any subsequent desired decomposition step.
Fig. 2 is a diagrammatic flow diagram of a continuous nickel deposition process self-contained with respect to CO, according to the invention. It shows generally as 10, a reaction chamber 12 linked to decomposition chamber 14 by Ni(C0)4 and CO conduits 16 and 18, respectively.
Chamber 12 contains, alternatively, nickel source 20 and resultant nickel 22, and has hydrogen feed and outlet/recycle conduits 24 and 26, respectively; HCI feed and outlet/recycle conduits 28 and 30, respectively; and Ni(C0)4/CO exit conduit 16.
Decomposition chamber 14 contains a substrate 32 to be nickel coated from line 16.
In operation, nickel source 20 is treated with hydrogen, typically, at 400-500 C for 5-15 hours and 2 1/min at atmosphere pressure to produce a reduced nickel powder 2 1.
HCI gas at 1 1/min and 50 - 80 is then recycled through chamber 12, optionally, with hydrogen, to produce treated nickel powder 22. Chamber 12 is then subsequently purged with, for example, argon from conduit 23 and, thereafter, CO from conduit 18 is fed into chamber 12, wherein Ni(C0) 4 is produced and passed through conduit 16 to decomposition chamber 14. Recycle conduit as shown in Fig. 2 are utilized as desired.
It can be seen that once the process is operating at "steady state" for an alternative two-stage operative cycle, that the amount of CO used in the production of Ni(CO)4 can be met from the decomposition thereof in chamber 14. The process can thus be considered as being essentially selfcontained with respect to CO.
t C,, ; . . : I. . Importantly, since the rate of production of Ni(CO)4 in chamber 12 is sufficiently high enough to warrant a direct feed to chamber 14 for decomposition of Ni onto substrate 32 in an efficacious manner, no intervening storage facility is -equired. This is of value in commercial operations.
S Fig. 3 shows generally as 100 a double chamber apparatus for the continuous production and decomposition of Ni(CO)4.
Ni(COh production chamber 120 contains activated nickel 140 prepared according to the invention, either in an initial starting amount as shown in this embodiment or under continuous feed means of an alternative embodiment (not shown). Chamber 120 has a CO feed inlet 160, whereby in operation CO gas reacts with nickel 140 to produce Ni(C0)4 at an acceptable production rate selected from 0.1 to 3.0 gNi(CO)4/g activated Ni/hr.
Decomposition chamber 180 contains a mandrel, mold or like substrate 200 having a substrate surface 220 upon which is deposited Ni as a coating 240 which constitutes a Ni shell product in the embodiment shown by decomposition of gaseous Ni(CO)4 from chamber 120 fed through conduit 260. By-product CO exits chamber through outlet 280 and is recycled through conduit 300 to feed inlet 160. The above process constitutes a continuous, CO self-contained system wherein the Ni(CO)4 is essentially produced in chamber 120 at a rate sufficient to provide for the practical deposition operation in chamber 180 as to negate the need for Ni(CO)4 storage with its attendant capital and operating costs.
Although this disclosure has described and illustrated certain preferred embodiments of the invention, it is to be understood that the invention is not restricted to those particular embodiments. Rather, the invention includes all embodiments which are functional or mechanical equivalents of the specific embodiments and features that have been described and illustrated. . : c:.
Claims (22)
- Clauns 1. A process for producing Ni(CO)4 from carbon monoxide and asource of nickel selected from the group consisting of elemental nickel, a nickel compound or mixtures thereof, provided said nickel compound is not nickel chloride Mar se or in admixture with a nickel carbonate ore in an amount greater than 50% w/w nickel chloride which process comprises (a) treating said nickel source with hydrogen at a pressure of at least atmospheric pressure and an effective temperature, in the presence of chloride anion or an In situ generator thereof precursor; to produce a resultant active nickel; and (b) to reacting said carbon monoxide with said resultant active nickel to produce said Ni(CO)4.
- 2. A process as defined in claim l wherein said nickel compound is selected from the group consisting of a nickel salt, nickel hydroxide, nickel carbonate and nickel oxide.
- 3. A process as defined in claim l or claim 2 wherein said chloride anion is present from a compound selected from hydrogen chloride and a metallic chloride.
- 4. A process as defined in any one of claims 1 to 3 wherein said metallic chloride is selected from the group consisting of an alkali, alkaline earth and transition metal chloride.
- 5. A process as defined in any one of claims 1 to 4 wherein said chloride anion is present as gaseous hydrochloric acid in gaseous admixture with said hydrogen.
- 6. A process as defined in any one of claims 1 to 5 wherein said nickel compound is first treated with hydrogen at said effective temperature for a first - period of time and subsequently treated with said gaseous admixture for a second period of time, at said effective temperature.
- 7. A process as defined in claim 5 or claim 6 wherein said nickel compound comprises nickel carbonate and said gaseous admixture comprises HCI and H2 in the molar ratio of about 1:2.
- 8. A process as defined in any one of claims I to 7 wherein said nickel compound is nickel carbonate.
- 9. A process as defined in any one of claims 1 to 8 wherein said nickel compound is nickel chloride. c r
- 10. A process as defined in any one of claims I to 9 wherein said effective temperature is selected from the range 300 - 650 C.
- 11. A process as defined in claim 10 wherein said effective temperature is selected from 350 - 550 C.
- 12. A process as defined in any one of claims 1 to 11 wherein said resultant active nickel is reacted with carbon monoxide at a temperature of about 50 C.
- 13. A process as defined in any one of claims 1 to 12 wherein said Ni(CO) 4 is produced in step (b) at an acceptable conversion rate, and further comprising passing said Ni(CO) directly to a decomposition chamber and decomposing said Ni(CO)4 to deposit nickel and CO.
- 14. A process as defined in claim 13, wherein said decomposition - effects deposition of Ni.
- 15.A process as defined in claim 13 or claim 14 wherein said acceptable conversion rate produce Ni(CO)4 at a rate of at least 0.1 g/hr Ni(C0)4 per g Ni.
- 16. A process as defined in claim 15 wherein said acceptable conversion rate is at least 0.25 g/hr Ni(CO)4 per g Ni.
- 17.A process as defined in claim 16 wherein said acceptable conversion rate produces Ni(CO)4 at a rate of 3.0 g/hr. Ni(CO)4 per g Ni.
- 18. A process as defined in any one of claims I to 17 wherein said precursor is selected from the group consisting of Cl2, oxides of chlorine and NaOCI.
- 19. A process for producing a resultant active nickel compound of subsequent use in the production of Ni(C0)4 by reaction with carbon monoxide, from a nickel source selected from the group consisting of elemental nickel, a nickel compound or mixtures thereof, which process comprises (a) treating said nickel source with hydrogen at a pressure of at least atmospheric pressure and an effective temperature, in the presence of chloride anion or an In situ generator thereof precursor as defined in any one of claims I to 18, and collecting said resultant active nickel.
- 20. A resultant nickel produced by a process as defined in any one of claims 13 tol7.
- 21. An improved apparatus for the production of nickel powder, coatings, articles or compounds from the decomposition of Ni(C0)4 said apparatus comprising: . .. . .. . . . . . :. :(a) a decomposition chamber having a Ni(C0)4 feed inlet, a spent CO outlet and adapted to receive a substrate; (b) a Ni(CO)4 production chamber having a CO feed inlet, a gaseous Ni(CO) 4 product outlet and adapted to receive source nickel for reaction with CO, wherein the improved apparatus comprises (i) Ni(C0)4 direct feed means between said Ni(C0)4 feed inlet of said decomposition chamber for feeding Ni(C0)4 directly from said production chamber to said decomposition chamber at an acceptable feed rate: (ii) CO recycle conduit means between said spent CO outlet and said CO feed inlet; and (iii)wherein said source nickel comprises activated nickel produced according to any one of claims 1 to 20.
- 22. Apparatus as defined in claim 21 wherein said direct feed means comprises means for feeding said Ni(C0)4 to said decomposition chamber at a rate of at least 0.1 gear. Ni(C0)4 per g said source nickel. .; r;1: . . . ! . . ; ' .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0606438A GB2425130B (en) | 2003-03-27 | 2004-03-24 | Apparatus for the production of nickel powder, nickel coatings, nickel articles or compounds thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/397,425 US7198770B2 (en) | 2002-12-04 | 2003-03-27 | Process for producing nickel carbonyl, nickel powder and use thereof |
Publications (3)
Publication Number | Publication Date |
---|---|
GB0406594D0 GB0406594D0 (en) | 2004-04-28 |
GB2399815A true GB2399815A (en) | 2004-09-29 |
GB2399815B GB2399815B (en) | 2007-06-27 |
Family
ID=32230124
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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GB0606438A Expired - Lifetime GB2425130B (en) | 2003-03-27 | 2004-03-24 | Apparatus for the production of nickel powder, nickel coatings, nickel articles or compounds thereof |
GB0406594A Expired - Lifetime GB2399815B (en) | 2003-03-27 | 2004-03-24 | Process for producing nickel carbonyl, nickel powder and use thereof |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
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GB0606438A Expired - Lifetime GB2425130B (en) | 2003-03-27 | 2004-03-24 | Apparatus for the production of nickel powder, nickel coatings, nickel articles or compounds thereof |
Country Status (4)
Country | Link |
---|---|
AU (1) | AU2004201188B8 (en) |
CA (1) | CA2461624C (en) |
GB (2) | GB2425130B (en) |
ZA (1) | ZA200402339B (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1591178A1 (en) * | 2004-04-27 | 2005-11-02 | Falconbridge Limited | Production of active nickel powder and transformation thereof into nickel carbonyl |
AU2005234712B1 (en) * | 2005-11-21 | 2007-05-24 | Cvmr Corporation | Re-activation of de-activated nickel for nickel carbonyl production |
US7452808B2 (en) | 2000-07-07 | 2008-11-18 | Chartered Semiconductor Manufacturing Ltd. | Method of copper/copper surface bonding using a conducting polymer for application in IC chip bonding |
US7776129B2 (en) | 2007-04-24 | 2010-08-17 | Chemical Vapour Metal Refining Inc. | Apparatus and process for making high purity nickel |
GB2449280B (en) * | 2007-05-17 | 2012-12-19 | Cvmr Corp | Apparatus and process for making high purity nickel |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1986430B (en) * | 2005-12-19 | 2012-05-16 | 雷普罗泰克有限公司 | Method and device for reactivating inactivated nickel for carbonyl nickel production |
AU2013212498A1 (en) * | 2012-01-27 | 2014-08-21 | Cvmr Corporation | Process for recovering metals from silicate materials |
CN105463199B (en) * | 2015-11-30 | 2017-12-12 | 金川集团股份有限公司 | A kind of method for reducing carbonyl nickel distillation process nickel plating |
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GB813819A (en) * | 1955-12-02 | 1959-05-21 | Montedison Spa | Process for preparing nickel carbonyl |
GB1099464A (en) * | 1963-10-24 | 1968-01-17 | Alberta Res Council | Composition of matter convertible to stable metallic form by hydrogen reduction |
GB1401718A (en) * | 1972-02-09 | 1975-07-30 | Int Nickel Canada | Treatment of nickeliferous oxide ores |
JPS562136B1 (en) * | 1968-02-08 | 1981-01-17 | ||
JPS58171506A (en) * | 1982-04-01 | 1983-10-08 | Sumitomo Metal Mining Co Ltd | Manufacture of fine metallic nickel powder |
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BE370325A (en) * | 1929-08-17 | 1900-01-01 | ||
CA879003A (en) * | 1969-03-28 | 1971-08-24 | The International Nickel Company Of Canada | Separation of nickel from cobalt |
CA2296964A1 (en) * | 2000-01-25 | 2001-07-25 | Chemical Vapour Metal Refining Inc. | Cobalt recovery process |
-
2004
- 2004-03-22 AU AU2004201188A patent/AU2004201188B8/en not_active Expired
- 2004-03-22 CA CA002461624A patent/CA2461624C/en not_active Expired - Lifetime
- 2004-03-24 GB GB0606438A patent/GB2425130B/en not_active Expired - Lifetime
- 2004-03-24 GB GB0406594A patent/GB2399815B/en not_active Expired - Lifetime
- 2004-03-25 ZA ZA200402339A patent/ZA200402339B/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB813819A (en) * | 1955-12-02 | 1959-05-21 | Montedison Spa | Process for preparing nickel carbonyl |
GB1099464A (en) * | 1963-10-24 | 1968-01-17 | Alberta Res Council | Composition of matter convertible to stable metallic form by hydrogen reduction |
JPS562136B1 (en) * | 1968-02-08 | 1981-01-17 | ||
GB1401718A (en) * | 1972-02-09 | 1975-07-30 | Int Nickel Canada | Treatment of nickeliferous oxide ores |
JPS58171506A (en) * | 1982-04-01 | 1983-10-08 | Sumitomo Metal Mining Co Ltd | Manufacture of fine metallic nickel powder |
Non-Patent Citations (1)
Title |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7452808B2 (en) | 2000-07-07 | 2008-11-18 | Chartered Semiconductor Manufacturing Ltd. | Method of copper/copper surface bonding using a conducting polymer for application in IC chip bonding |
EP1591178A1 (en) * | 2004-04-27 | 2005-11-02 | Falconbridge Limited | Production of active nickel powder and transformation thereof into nickel carbonyl |
WO2005102569A1 (en) * | 2004-04-27 | 2005-11-03 | Falconbridge Limited | Production of active nickel powder and transformation thereof into nickel carbonyl |
AU2005234712B1 (en) * | 2005-11-21 | 2007-05-24 | Cvmr Corporation | Re-activation of de-activated nickel for nickel carbonyl production |
US7776129B2 (en) | 2007-04-24 | 2010-08-17 | Chemical Vapour Metal Refining Inc. | Apparatus and process for making high purity nickel |
US8852315B2 (en) | 2007-04-24 | 2014-10-07 | Cvmr Corporation | Apparatus and process for making high purity nickel |
GB2449280B (en) * | 2007-05-17 | 2012-12-19 | Cvmr Corp | Apparatus and process for making high purity nickel |
Also Published As
Publication number | Publication date |
---|---|
GB0406594D0 (en) | 2004-04-28 |
CA2461624C (en) | 2005-10-18 |
AU2004201188B8 (en) | 2005-07-14 |
GB2399815B (en) | 2007-06-27 |
ZA200402339B (en) | 2004-06-07 |
GB0606438D0 (en) | 2006-05-10 |
GB2425130B (en) | 2007-05-09 |
AU2004201188B2 (en) | 2005-05-26 |
CA2461624A1 (en) | 2004-09-27 |
AU2004201188A1 (en) | 2004-10-14 |
GB2425130A (en) | 2006-10-18 |
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