AU2005306521A1 - Method for producing fine, low bulk density, metallic nickel powder - Google Patents
Method for producing fine, low bulk density, metallic nickel powder Download PDFInfo
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- AU2005306521A1 AU2005306521A1 AU2005306521A AU2005306521A AU2005306521A1 AU 2005306521 A1 AU2005306521 A1 AU 2005306521A1 AU 2005306521 A AU2005306521 A AU 2005306521A AU 2005306521 A AU2005306521 A AU 2005306521A AU 2005306521 A1 AU2005306521 A1 AU 2005306521A1
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- Australia
- Prior art keywords
- nickel
- bulk density
- fine
- low bulk
- powder
- Prior art date
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Classifications
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- 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
- C22B23/021—Obtaining nickel or cobalt by dry processes by reduction in solid state, e.g. by segregation processes
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- 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
- B22F9/20—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from solid metal compounds
- B22F9/22—Making metallic powder or suspensions thereof using chemical processes with reduction of metal compounds starting from solid metal compounds using gaseous reductors
-
- 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
- C22B5/00—General methods of reducing to metals
- C22B5/02—Dry methods smelting of sulfides or formation of mattes
- C22B5/12—Dry methods smelting of sulfides or formation of mattes by gases
Description
WO 2006/053418 PCT/CA2005/001144 1 TITLE OF THE INVENTION [0001] Method for producing fine, low bulk density, metallic nickel powder. FIELD OF THE INVENTION [0002] The present invention relates to a method for producing a fine, low bulk density, metallic nickel powder. BACKGROUND OF THE INVENTION [0003] Canadian application No. 2,418,063 teaches how to produce an active nickel powder by reducing a nickel chloride containing salt having a high surface area with hydrogen gas at a temperature above 3000C, and how to rapidly convert such active powder to nickel carbonyl. However, this patent application does not address the deleterious issue of particle agglomeration during the production of active nickel powder. [0004] Indeed, it is known that freshly reduced metallic nickel particles exhibit a great affinity for each other and for the inner surfaces of the furnace, and can readily form growing agglomerates. These agglomerates thwart attempts at producing a fine, low bulk density, metallic nickel powder. [0005] Prior art teaches several methods said to limit agglomeration of nickel particles during reduction. [0006] US Patent 3,914,124 teaches the use of at least one additive selected from the group consisting of "calcium oxide, magnesia or compounds that are heat decomposable thereto" (abstract), to create an anti-agglomerating WO 2006/053418 PCT/CA2005/001144 2 coating on a substantial portion of the particles to minimise sticking while reducing nickel oxide. However, the process disclosed requires very high temperatures to assure a low volatile impurity content. [0007] Canadian Patent 2,204,525 teaches the use of an organic 5 dispersant such as gelatin and/or bone glue as an anti-agglomerating agent, as well as of a spheroid-promotion agent such as anthraquinone. However, the process disclosed results in the formation of a high density nickel powder, as opposed to low density nickel powder. [0008] The use of fluidized beds has also been suggested (GB Patent 10 No. 769099) but has not helped to avoid agglomeration since such beds tend to collapse when the reduction of nickel containing compounds to metallic nickel powder exceeds 70% and particles begin to agglomerate. [0009] US Patent 2,948,525 teaches the use of a kiln with a completely continuous oxide film, such as aluminium oxide, which is irreducible at the 15 temperature used for reduction of nickel compounds, so as to eliminate sticking of the nickel powder to the kiln walls. However, this patent does not solve the problem of inter-particles sticking and agglomerating. [0010] It is also known that when reducing a furnace charge of solid particles with a gas, it is desirable to maximize the contact between each 20 particle and the reducing gas. This is often achieved by moving the furnace charge during the reduction phase, for example, in a rotating kiln or a fluidized bed. However, it has been found that reducing a nickel containing charge in a rotating kiln operating at a typical rotation rate of about 10 rpm, results in a coarse fraction containing some hard agglomerate lumps, exceeding 1.3 cm in 25 diameter. Such an end product does not have enough reactivity for a possible further chemical treatment, for example, to produce nickel carbonyl. Moreover, WO 2006/053418 PCT/CA2005/001144 3 it has been observed that in a rotating kiln, for example, the formation of agglomerates and lumps increases as the rate of kiln rotation increases. [0011] Thus, vigorous agitation during reduction results in production of hard agglomerates, which cannot subsequently be crushed to powder. In 5 attempts to break-up the agglomerates of nickel powder during reduction, it was found that the addition of ceramic or metallic balls to the kiln charge was not successful. The balls become rapidly hard-coated with nickel powder and continue to grow in size. [0012] As noted above, prior art processes fail to solve the difficulty of 10 making fine, low bulk density, nickel powder. Thus there remains a need for a method for preparing fine, low bulk density nickel powder while minimising non friable particle agglomerates. [0013] The present invention seeks to meet this and other needs. SUMMARY OF THE INVENTION 15 [0014] It has been found that a fine, low bulk density, metallic nickel powder can be produced by treating reducible nickel salts with a hydrogen containing gas, at temperatures ranging from about 3000C to about 500*C, while the extent of movement and the average kinetic energy of the freshly produced metallic nickel particles are minimised. This method has been found 20 to significantly reduce formation.of nickel agglomerates. [0015] It has also been found that during reduction, soft agglomerates can be produced when gentle agitation is used. In contrast to the hard agglomerates produced by some of the prior art processes, these soft agglomerates are friable and can subsequently be crushed quite easily to 25 powder and mostly break up during product screening.
WO 2006/053418 PCT/CA2005/001144 4 [0016] More specifically, the present invention relates to a method of producing a fine, low bulk density nickel powder, comprising: a) charging particles of at least one reducible nickel salt within a furnace so as to form a moving bed of furnace charge; and 5 b) reducing the furnace charge with a H 2 containing gas at a temperature ranging from about 3000C to about 500*C; the bed of furnace charge being moved gently so as to minimise formation of hard agglomerates and thereby obtaining a fine, low bulk density nickel powder. 10 [0017] The present invention also relates to a method of producing a fine, low bulk density nickel powder, comprising: a) charging particles of at least one reducible nickel salt within a furnace so as to form a static, shallow bed of furnace charge; and b) reducing the furnace charge with a H 2 containing gas at a 15 temperature ranging from about 3000C to about 500*C; the static bed of furnace charge being shallow so as to allow penetration of reducing gas into the bed and minimise formation of hard agglomerates, thereby obtaining a fine, low bulk density nickel powder. [0018] Other objects, advantages and features of the present invention 20 will become more apparent upon reading of the following non-restrictive description of preferred embodiments thereof, given by way of example only with reference to the accompanying drawings.
WO 2006/053418 PCT/CA2005/001144 5 BRIEF DESCRIPTION OF THE DRAWINGS [0019] In the appended drawings: [0020] Figure 1 is a graph illustrating the effect of reducing the rotation rate of a kiln having an internal diameter of 10.2 cm on the quantity of metallic 5 nickel powder passing various screens (size fractions are indicated in microns); [0021] Figure 2 is a graph illustrating the effect of varying the rotation rate of a kiln having an internal diameter of 10.2 cm on the quantity of metallic nickel powder passing through a 65 mesh screen (210 microns); [0022] Figure 3 is a graph illustrating the effect of varying the rotation 10 rate of a kiln having an internal diameter of 10.2 cm on the quantity of metallic nickel powder passing through a 100 mesh screen (149 microns); [0023] Figure 4 is a flowchart of a preferred embodiment of the present invention; [0024] Figure 5 is an electromicrograph of a dry free-flowing powder of 15 nickel carbonate and nickel hydroxide used as a feed in Example 1, and as typically used in the method of the present invention (AMRAY Scanning electron microscope, x500 magnification); and [0025] Figure 6 is an electromicrograph of a fine, low bulk density metallic nickel powder as obtained according to the method of the present 20 invention (AMRAY Scanning electron microscope, x500 magnification).
WO 2006/053418 PCT/CA2005/001144 6 DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS [0026] The present invention is illustrated in further details by the following non-limiting examples. [0027] In general terms, the present invention relates to a method for 5 producing a fine, low bulk density, unagglomerated or friable, metallic nickel powder by reducing, in a hydrogen containing gas, a furnace charge that is either static or moved gently so as to minimise the average kinetic energy of these freshly reduced particles. [0028] As used herein when referring to either a feed or a product, the 10 term "particle" designate any small piece or part of a flowable material, such as a powder. [0029] As used herein, the term "agglomerate" refers to a group of individual particles sticking together to form either a soft or hard lump. [0030] As used herein when referring to a nickel powder, the term "fine" 15 means that at least about 45% of the powder would pass through a 100 mesh (149 microns) screen, with essentially no remaining hard agglomerates in the +100 mesh fraction. [0031] As used herein when referring to a nickel powder obtained by the method of the present invention, the term "low bulk density" means a bulk 20 density of 4 g/cc or less. Preferably, nickel powders obtained by the method of the present invention have a bulk density between about 0.5 and about 2 g/cc. Most preferably, nickel powders obtained by the method of the present invention have a bulk density between about 0.5 and about 1.6 g/cc.
WO 2006/053418 PCT/CA2005/001144 7 [0032] As used herein when referring to a static bed of furnace charge, the term "shallow" defines a depth of powder charge that would allow the penetration of reducing gas into the bed. Usually, such static shallow bed is about 2.5 cm deep or less. 5 [0033] As used herein when referring to numerical values or percentages, the term "about" includes variations due to the methods used to determine the values or percentages, statistical variance and human error. Moreover, each numerical parameter in this application should at least be construed in light of the number of reported significant digits and by applying 10 ordinary rounding techniques. [0034] It is quite counter-intuitive to minimise the rotation rate of a kiln when searching to achieve an acceptable reduction rate and an acceptable reduction product, since this action limits both the gas-solid interaction and the rate of charge throughput. 15 [0035] However, it was unexpectedly discovered that reducing the rotation rate of the kiln, thus reducing the peripheral speed of the kiln during reduction, resulted in less agglomeration and increased the amount of fine nickel powder product. The effect of lowering the rotation rate of a kiln having an internal diameter of 10.2 cm on the amounts of nickel powder product 20 passing various screens is illustrated in Figure 1. For example: reducing the rotation rate from 2 rpm to 0.8 rpm reduces the proportion of the fraction above 150 microns in diameter (+100 mesh) from about 72% to about 53%; and reducing the rotation rate from 2 rpm to 0.2 rpm allows reducing the proportion of +100 mesh fraction from about 72% to about 48%. 25 [0036] Similar data can be seen from another angle in Figures 2 and 3, illustrating the effects of varying the rotation rate of a kiln having an internal WO 2006/053418 PCT/CA2005/001144 8 diameter of 10.2 cm on the amounts of nickel powder passing through a 65 and a 100-mesh screen, respectively. [0037] The screening measures referred to in this application were performed on a well-known Ro-TapTM machine, in which the screens are 5 shaken and tapped. The screening period used was usually 20 min. [0038] The method according to the present invention utilizes either a static or slowly moving furnace charge. [0039] The method itself can be performed either continuously or batch wise. 10 [0040] The reduction temperature ranges from about 3000C to about 5000C, preferably from about 3500C to about 450 C. [0041] In a particular embodiment, the reducing gas contains at least 20% hydrogen in volume. [0042] In another particular embodiment, the hydrogen containing gas is 15 preheated before entering the kiln. [0043] In still another particular embodiment, the feed of reducible nickel salt is calcinated in a nitrogen or other inert gas atmosphere at a temperature ranging from about 300 to about 3500C. This is done in either the first compartment of the furnace or in a separate furnace. 20 [0044] Such calcination of the feed drives off carbon dioxide gas from the nickel carbonate in thefeed and thus allows separate scrubbing and WO 2006/053418 PCT/CA2005/001144 9 removal of carbon dioxide. This simplifies the cleaning of the off-gas from the reduction step and allows the recycling of unused hydrogen. [0045] It is to be understood that both the preheating of the gas and the calcination can occur within the same particular embodiment of the method 5 according to the present invention. [0046] One of the preferred embodiments of the present invention is illustrated on Figure 4. The dry free flowing powder of reducible nickel salt (1) is calcinated in a first furnace in presence of nitrogen gas (2). The off-gas of calcination (4) essentially contains CO 2 , CO, H 2 0 and N 2 . The hot calcine (3) is 10 then transferred into a second furnace, namely the reduction kiln, so as to form a bed of furnace charge. H 2 gas (5) is advantageously passed into the static or slowly moving bed of furnace charge, and an excess of H 2 is advantageously used. Such a process allows obtaining a fine, low bulk density nickel powder (6). Thanks to the separate calcination step, the off-gas of the reduction kiln 15 only contains H 2 and H 2 0, which allows an easy H 2 recycling. [0047] The exact composition of the feed of reducible nickel salt used in the method of the present invention may of course influence the final bulk density and fineness of the nickel powder product. [0048] Indeed, it has been found that the bulk density of the nickel 20 powder product increased as the total amount of inert impurities in the feed material decreased. Inert impurities are typically various amounts of carbonate/chloride/sulphate salts of sodium/magnesium/calcium. This is illustrated in Table 1 below. Thus, the bulk density of nickel powder product decreased from 1.2 g/cc to 0.5 g/cc as the total amount of inert impurities 25 increased from about 10 wt% (well-washed nickel carbonate) to about 30 wt% (poorly washed nickel carbonate).
WO 2006/053418 PCT/CA2005/001144 10 Table 1: composition (in wt%) and bulk densities of well-washed and poorly washed nickel carbonate bulk bulk density density before after Feed: reduction reduction well washed 46.0 10.9 2.46 2.43 0.29 0.4 0.9 g/cc 1.2 g/cc nickel carbonate poorly washed 36.6 8.6 5.3 5.41 0.15 0.2 0.8 g/cc 0.5 g/cc nickel carbonate [0049] Initially, the bulk densities of feed materials and nickel powder products referred to in this application were measured by filling a graduated cylinder with a known volume of powder and then weighing the cylinder. Reproducible results were obtained by tapping the cylinder to consolidate the 5 powder three times during the preparation. Subsequently, the bulk densities of, feed materials and nickel powder products were measured with a Scott Volumeter employing ASTM standard method B329-98. [0050] As stated above, the feed composition also has an influence on the fineness of the metallic nickel powder product, as illustrated in Table 2 10 below. Table 2: Influence of the nickel carbonate feed impurities on fineness of nickel powder product Degree o RPM of wt% passing wt% passing washing kiln through a 65 through a 100 mesh screen mesh screen well-washed 0.2 53.6 45.7 feed regularly 0.2 59.6 51.3 washed feed poorly 0.2 99.7 99.5 washed feed WO 2006/053418 PCT/CA2005/001144 11 [0051] Table 2 shows that, as the degree of washing of the nickel carbonate decreases, and therefore the inert impurity content increases, the nickel powder obtained according to the process of the present invention becomes much finer. Indeed, at least 99% of the final product obtained from a 5 poorly washed nickel carbonate feed (about 30 wt% inert impurities) pass through a 100 mesh screen. [0052] The reducible nickel salts used in the method of the present invention are preferably nickel carbonate, nickel oxide, nickel hydroxide, nickel oxalate. Those skilled in the art will appreciate that any other fine, low density 10 nickel compound that is reduced to a metallic state in hydrogen gas below 5000C can also be used. For example, nickel chloride may be used. However, nickel chloride, either hydrated or not, or other reducible nickel salts that happen to melt or become sticky below 500*C, can be used as feed in the method of the present invention only when used in combination with at least 15 another reducible nickel salt of the above category, such as the preferred cited salts. [0053] It is to be understood that many other operating parameters and processing conditions can be easily varied by a person skilled in the art without departing from the method of the present invention. Such parameters and 20 conditions are (but not limited to): reducing gas flow rate and composition, co current or counter-current kiln -operation, kiln length and furnace charge residence time and back mixing of nickel powder product with fresh feed. EXAMPLE 1 [0054] Fine, low bulk density nickel powders were prepared according to 25 the method of the present invention in a rotating kiln with an internal diameter of about 10.2 cm (4 inches). In a batch process, charges of 300 to 500g of nickel carbonate were used. The reduction temperature was 4500C and a WO 2006/053418 PCT/CA2005/001144 12 hydrogen gas flow at 2 Ipm was provided to the feed in a kiln rotating at 0.2 rpm, corresponding to a peripheral velocity of 6.4 cm/min (see formula below). The residence time of the feed in the kiln was 3/2 to 4 hours. Peripheral velocity = internal diameter x Pi x rotation rate 5 (cm/min) (cm) (rpm) [0055] Illustration of nickel carbonate feed as used and of nickel powder as produced in this Example is provided in the electromicrographs of Figures 5 and 6, respectively. [0056] The bulk densities of nickel powders produced in the rotating kiln 10 used in this example varied between 0.46 and 1.58 g/cc, as shown in Table 3 below. Table 3: Bulk Densities of -100 Mesh Fraction (g/cc) Test ',Weight Volume Bulk Density, Average bulk g cc g/cc Density g/cc 1 7.883 7.2 1.09 6.247 5.5 1.14 8.528 7.6 1.12 1.12 2 9.789 .7.1 1.38 6.649 5 1.33 11.034 7.85 1.41 1.37 3 3.557 7.5 0.47 3.904 8.5 0.46 2.833 6.2 0.46 0.46 4 9.843 7.8 1.26 10.8905 8.575 1.27 11.938 9.35 1.28 1.27 5 8.8 5.4 1.63 9.9 6.4 1.55 8.4 5.35 1.57 1.58 6 6.7 7.7 0.87 7.2 8 0.90 5.5 6.6 0.83 0.87 WO 2006/053418 PCT/CA2005/001144 13 EXAMPLE2 [0057] Fine, low bulk density nickel powders were prepared according to the method of the present invention in a rotating kiln with an.internal diameter of about 30.5 cm (12 inches). In a batch process, charges of 3.5 kg of nickel 5 carbonate were used. The reduction temperature was 450'C and a hydrogen gas flow at 3 Ipm was provided to the feed in a kiln rotating at 0.07 rpm, corresponding to a peripheral velocity of 6.7 cm/min. The residence time of the feed in the kiln was 6 to 7 hours. EXAMPLE 3 10 [0058] Fine, low bulk density nickel powders were prepared according to the method of the present invention in a rotating kiln with an internal diameter of about 61 cm (24 inches). In a continuous process, 7 to 8 kg per hour of nickel carbonate were fed to the kiln. The reduction temperature was 350 to 4000C in the first half of the kiln and 4500C in the second half of the kiln. 15 Hydrogen and nitrogen gases were fed at 85 and 42.5 Ipm, respectively, in the kiln rotating at 0.125 rpm, corresponding to a peripheral velocity of 23.9 cm/min. The residence time of the feed in the kiln was about 20 hours. [0059] The peripheral velocity used in the kiln having an internal diameter of 61 cm was higher than that used with the smaller diameter kilns 20 (examples 1 and 2) so that an acceptable economical powder production rate could be achieved. [0060] In this example, nickel powder was produced using two passes through the kiln. During the first pass, preheating in nitrogen gas was used to drive off carbon dioxide from the nickel carbonate in the feed material. In the 25 second pass through the kiln, the furnace charge was reduced with hydrogen gas to a low bulk density nickel powder. Typical kiln conditions for the preheating step were as follows: kiln rotation rate 0.22 rpm, kiln slope 0.014 WO 2006/053418 PCT/CA2005/001144 14 feet/foot, kiln shell temperatures feed end: 3300C, product end 450 to 4600C, nitrogen gas flow 100 litres per minute, C02 in off gas 22 volume %, feed rate 16 to 17 kg/hour. [0061] Although the present invention has been described herein above 5 by way of preferred embodiments thereof, it can be modified, without departing from the spirit and nature of the subject invention as defined in the appended claims.
Claims (19)
1. A method of producing a fine, low bulk density nickel powder, said method comprising: a) charging particles of at least one reducible nickel salt within 5 a furnace so as to form a moving bed of furnace charge; and b) reducing said furnace charge with a H 2 containing gas at a temperature ranging from about 3000C to about 5000C, said bed of furnace charge being moved gently so as to minimise formation of hard agglomerates and thereby obtaining a fine, low bulk density nickel 10 powder.
2. The method according to claim 1, further comprising: c) collecting said fine, low bulk density nickel powder; and d) screening said fine, low bulk density nickel powder, thereby producing an essentially unagglomerated, low -bulk density 15 nickel powder.
3. The method according to claim 1 or 2, wherein said furnace is a rotating kiln operating with a peripheral velocity of less than about 25 cm per minute.
4. The method according to claim 1, employing a continuous production of said fine, low bulk density nickel powder. 20
5. The method according to claim 1, employing a batch-wise production of said fine, low bulk density nickel powder.
6. The method according to claim 1, wherein said hydrogen containing gas contains at least 20 volume percent hydrogen. WO 2006/053418 PCT/CA2005/001144 16
7. The method according to claim 1, wherein said hydrogen containing gas is in excess during the reduction step.
8. The method according to claim 1, wherein said reducible nickel salts are in form of a dry powder. 5
9. The method according to claim 1 or 8, wherein said reducible nickel salts are calcinated in nitrogen or another inert gas in either a first compartment of the furnace or in a separate furnace.
10. The method according to claim 1, 8 or 9, wherein said hydrogen containing gas is preheated before the reduction step. 10
11. The method according to claim 9 or 10, wherein said calcination is made at a temperature ranging from about 300 to about 350*C.
12. The method according to claim 10 or 11, wherein said preheating is made at a temperature ranging from about 300 to about 3500C.
13. The method according to claim 1, wherein said reducible nickel salts 15 include nickel carbonate.
14. The method according to claim 1, wherein said reducible nickel salt includes salts selected from the group consisting of nickel oxide, nickel hydroxide and nickel oxalate.
15. The method according to claim 1, wherein said reduction temperature 20 ranges from about 350 to about 4500C.
16. A method of producing a fine, low bulk density nickel powder, comprising: a) charging particles of at least one reducible nickel salt within a furnace so as to form a static, shallow bed of furnace charge; WO 2006/053418 PCT/CA2005/001144 17 b) reducing said furnace charge with a H 2 containing gas at a temperature ranging from about 300'C to about 5000C, said static bed of furnace charge being shallow so as to allow penetration of reducing gas into the bed and minimise formation of hard agglomerates, 5 thereby obtaining a fine, low bulk density nickel powder.
17. The method according to claim 16, further comprising: c) collecting said fine, low bulk density nickel powder; and d) screening said fine, low bulk density nickel powder, thereby producing an essentially unagglomerated, low bulk density nickel 10 powder.
18. The method according to claim 2 or 16, wherein said screening is performed onto a 100-mesh screen.
19. The method according to claim 16, wherein said hydrogen containing gas is in excess during the reduction step.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2,488,077 | 2004-11-19 | ||
US10/993,622 US20060107792A1 (en) | 2004-11-19 | 2004-11-19 | Method for producing fine, low bulk density, metallic nickel powder |
CA 2488077 CA2488077A1 (en) | 2004-11-19 | 2004-11-19 | Method for producing fine, low bulk density, metallic nickel powder |
US10/993,622 | 2004-11-19 | ||
PCT/CA2005/001144 WO2006053418A1 (en) | 2004-11-19 | 2005-07-20 | Method for producing fine, low bulk density, metallic nickel powder |
Publications (1)
Publication Number | Publication Date |
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AU2005306521A1 true AU2005306521A1 (en) | 2006-05-26 |
Family
ID=36406793
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2005306521A Abandoned AU2005306521A1 (en) | 2004-11-19 | 2005-07-20 | Method for producing fine, low bulk density, metallic nickel powder |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1812611A4 (en) |
JP (2) | JP4961348B2 (en) |
AU (1) | AU2005306521A1 (en) |
BR (1) | BRPI0518440A2 (en) |
WO (1) | WO2006053418A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5794426B2 (en) * | 2011-11-30 | 2015-10-14 | 戸田工業株式会社 | Manufacturing method of nickel fine particle powder |
EP3164238B1 (en) * | 2014-07-02 | 2020-06-03 | INVISTA Textiles (U.K.) Limited | Nickel metal particle production |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2000171A (en) * | 1932-08-27 | 1935-05-07 | Falconbridge Nickel Mines Ltd | Reduction of oxygeneous nickel or nickel copper compounds |
US2616781A (en) * | 1948-12-17 | 1952-11-04 | Sherritt Gordon Mines Ltd | Treatment of nickeliferous oxide concentrates for recovery of nickel values therefrom |
US2677607A (en) * | 1950-10-24 | 1954-05-04 | Republic Steel Corp | Process of selectively reducing nickel chloride from a mixture containing nickel and iron chlorides to produce nickel |
US3684481A (en) * | 1970-07-27 | 1972-08-15 | Falconbridge Nickel Mines Ltd | High purity nickel product |
SE392043B (en) * | 1974-01-29 | 1977-03-14 | Varta Batterie | PROCEDURE AND DEVICE FOR CARRYING OUT REACTIONS BETWEEN POWDER AND GASY SUBSTANCES |
BE823966A (en) * | 1974-01-29 | 1975-04-16 | PROCEDURE FOR EXECUTING REACTIONS BETWEEN PULVERULENT SUBSTANCES AND GASEOUS SUBSTANCES | |
JPS59197506A (en) * | 1983-04-22 | 1984-11-09 | Hitachi Metals Ltd | Preparation of metal powder for magnetic recording |
JPS60131904A (en) * | 1983-12-21 | 1985-07-13 | Sumitomo Metal Mining Co Ltd | Manufacture of fine metallic nickel powder |
JPS6223912A (en) * | 1985-07-23 | 1987-01-31 | Showa Denko Kk | Production of fine metallic powder |
DE3528257A1 (en) * | 1985-08-07 | 1987-02-19 | Peter Dr Faber | Process for preparing sinterable nickel powder for electrode structures of alkaline batteries |
JPH1088205A (en) * | 1996-09-10 | 1998-04-07 | Sumitomo Metal Mining Co Ltd | Production of metallic nickel powder |
JP4831518B2 (en) * | 2001-09-19 | 2011-12-07 | 住友金属鉱山株式会社 | Method for producing nickel powder |
JP2003213310A (en) * | 2002-01-16 | 2003-07-30 | Sumitomo Metal Mining Co Ltd | Method for manufacturing nickel powder |
-
2005
- 2005-07-20 BR BRPI0518440-1A patent/BRPI0518440A2/en not_active IP Right Cessation
- 2005-07-20 WO PCT/CA2005/001144 patent/WO2006053418A1/en active Application Filing
- 2005-07-20 EP EP05764274A patent/EP1812611A4/en not_active Withdrawn
- 2005-07-20 AU AU2005306521A patent/AU2005306521A1/en not_active Abandoned
- 2005-07-20 JP JP2007541593A patent/JP4961348B2/en active Active
-
2011
- 2011-12-09 JP JP2011269857A patent/JP5650632B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
JP2008520824A (en) | 2008-06-19 |
JP4961348B2 (en) | 2012-06-27 |
JP5650632B2 (en) | 2015-01-07 |
BRPI0518440A2 (en) | 2008-11-18 |
EP1812611A1 (en) | 2007-08-01 |
EP1812611A4 (en) | 2009-04-01 |
WO2006053418A1 (en) | 2006-05-26 |
JP2012112044A (en) | 2012-06-14 |
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