WO2009132558A1 - A method of extracting ni and/or co - Google Patents
A method of extracting ni and/or co Download PDFInfo
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- WO2009132558A1 WO2009132558A1 PCT/CN2009/071388 CN2009071388W WO2009132558A1 WO 2009132558 A1 WO2009132558 A1 WO 2009132558A1 CN 2009071388 W CN2009071388 W CN 2009071388W WO 2009132558 A1 WO2009132558 A1 WO 2009132558A1
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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
- C22B23/04—Obtaining nickel or cobalt by wet processes
- C22B23/0407—Leaching processes
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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
- C22B23/005—Preliminary treatment of ores, e.g. by roasting or by the Krupp-Renn process
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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
- C22B23/04—Obtaining nickel or cobalt by wet processes
- C22B23/0407—Leaching processes
- C22B23/0415—Leaching processes with acids or salt solutions except ammonium salts solutions
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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
- C22B23/04—Obtaining nickel or cobalt by wet processes
- C22B23/0407—Leaching processes
- C22B23/0415—Leaching processes with acids or salt solutions except ammonium salts solutions
- C22B23/043—Sulfurated acids or salts thereof
Definitions
- the present invention relates to a method for extracting nickel and/or cobalt, and in particular to a method for extracting nickel and/or cobalt from laterite nickel ore, in particular by using limonite type and serpentine type laterite A method in which nickel ore is separately collected and treated to extract nickel, cobalt, or nickel and cobalt. It belongs to the field of hydrometallurgy.
- a method for extracting nickel, cobalt, or nickel and cobalt from laterite nickel ore includes a heap leaching process of laterite nickel ore and a normal pressure agitation leaching process.
- the serpentine type ore which can obtain the shorter leaching period by the available heap leaching process can not obtain the shorter leaching process with the heap leaching process.
- the periodic limonite-type ore is mixed and heated and stirred for leaching, resulting in too much processing capacity, high use of equipment, and high energy consumption.
- Another object of the present invention is to provide a method for extracting nickel and/or cobalt, which is simple in equipment
- Another object of the present invention is to provide a method of extracting nickel and/or cobalt which is low in energy consumption and cost effective.
- Another object of the present invention is to provide a method of extracting nickel and/or cobalt which has a high nickel leaching rate.
- the present invention provides a method for extracting nickel and/or cobalt, comprising a heap leaching process and a normal pressure heating and stirring leaching process, characterized in that the limonite type ore is cooled by atmospheric pressure stirring. Take; and the serpentine type ore is leached by heap leaching.
- nickel and cobalt, and nickel or cobalt are extracted from laterite nickel ore.
- the atmospheric pressure agitation leaching process of the limonite type ore comprises the following process steps:
- the leached slurry is filtered, and the filter residue is washed with water, and the resulting leaching solution is used to prepare a nickel-cobalt product.
- the heap leaching process of the serpentine type ore comprises the following process steps:
- leaching agent with a concentration of 5 ⁇ 15%, let it naturally infiltrate from the upper part into the bottom; and formulating the collected leachate to make the nickel ion concentration of the leachate reach 1.5 ⁇ 5g/L, for preparing nickel-cobalt products
- the leachate with a nickel ion concentration of less than 1.2 g/L is returned to the leaching.
- a leaching agent having a concentration of 5 to 15% is added from the top of the immersion column, and naturally flows into the bottom from the top for infiltration.
- the leaching agent is an aqueous solution containing sulfuric acid, hydrochloric acid, or a mixed acid thereof.
- the nickel-cobalt product is obtained from the obtained leachate.
- the ore particle size is controlled by crushing the ore.
- the ore having a particle size larger than lcm is crushed to control the ore particle size to be less than 1 cm; and the ore/immersion ore
- J(W/V) is 1.0:
- the ore having a particle diameter of more than 3 cm is crushed, the ore particle size is less than 3 cm, the ore water content is 25%; the ore layer thickness is 5 m; the sulfuric acid aqueous solution is prepared according to the leaching agent concentration of 10%, and the leaching agent is added to the top of the ore layer.
- the leaching agent concentration is added to the top of the ore layer.
- the serpentine-type ore in the laterite nickel ore is distilled to obtain a shorter leaching period and a high leaching rate, and the remaining limonite-type ore is heated and stirred at normal pressure. Leaching, making it easier [26]
- the serpentine type ore and the limonite type ore in the laterite nickel ore are respectively subjected to different leaching processes, and the serpentine type ore is subjected to a heap leaching process to obtain a faster leaching speed.
- the limonite type ore is leached by the atmospheric pressure heating and stirring process, thereby avoiding the problem that the heap leaching speed is extremely slow and the leaching period is long.
- the present invention is more suitable for the heap than the existing process of mixing the above two ores together for heap leaching or agitation leaching.
- the immersed serpentine ore is leached by a heap leaching method, which has a short cycle and a high leaching rate.
- the limonite type ore which is difficult to be leached is leached by the heating and stirring method, and the leaching rate is high, and the leaching rate is also high.
- such a combination process has better technical effects than a single heap leaching process or a single warming agitation leaching process.
- Figure 1 is a flow chart of atmospheric pressure stirring leaching process for preparing nickel-cobalt products from limonite ore.
- Figure 2 is a flow chart of column immersion (simulated heap leaching) for the preparation of nickel-cobalt products from serpentine ore.
- serpentine-type ores have a shorter leaching period in the heap leaching process, while limonite-type ores have a longer leaching period.
- the atmospheric pressure stirring leaching process for preparing nickel-cobalt products from limonite ore includes the following steps: ore preparation step 11, atmospheric pressure stirring leaching step 12, and solid/liquid separation Step 13, wherein the step 12 is performed by the inorganic acid application step 111, and the solid/liquid separation step 13 results in the production of the leachate 14 and the leach residue 15 for the nickel-cobalt product.
- A crushing ore with a particle size larger than lcm, controlling the ore particle size to be less than lcm;
- the nickel leaching rate is 82.37%; and the nickel-cobalt-containing leachate can be treated by the prior art to obtain a nickel-cobalt product.
- the ore/leaching agent (W/V) may be 1.0: 1.5 ⁇ 1.0: 2.5,
- the concentration of the leaching agent can be 20 ⁇ 30%, and the stirring temperature can be 70 ⁇ 100 °C.
- the leaching time can be 48 to 4 hours, and the object of the present invention can be achieved as well.
- the column leaching method (simulation heap leaching) leaching process for preparing nickel-cobalt products from serpentine ore includes the following steps: ore preparation step 21, column leaching (simulation heap leaching) steps 22.
- Leaching Night Density Judging Step 23 wherein the column immersion (simulation heap leaching) step 22 comprises the inorganic acid application step 211, with the result that the leaching solution 24 and the leaching slag 25 for producing the nickel-cobalt product are produced.
- the nickel-cobalt peak solution is concentrated in the early stage of leaching.
- the leachate is prepared to make the nickel ion concentration of the leachate reach 2g/L, which is used to prepare nickel-cobalt product.
- the nickel ion concentration is less than 1.2g/
- the leachate of L is used to return the leach.
- the nickel leaching rate was 84.9%.
- the nickel-cobalt-containing leachate can be treated by the prior art to obtain a nickel-cobalt product.
- the ore water content may be controlled to be greater than 20%; the material layer thickness may be 1 to 6 m, the concentration of the leaching agent may be 5 to 15%, and the leachate nickel ion concentration may be 1.5 to 5 g/ L, the object of the invention can also be achieved.
- the leaching agent is an aqueous solution containing sulfuric acid, hydrochloric acid, or a mixed acid thereof.
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Abstract
Description
说明书 一种提取镍和 /或钴的方法 Description A method for extracting nickel and/or cobalt
技术领域 Technical field
[1] 本发明涉及一种提取镍和 /或钴的方法, 特别是涉及一种从红土镍矿中提取镍 和 /或钴的方法, 尤其是通过将褐铁矿型和蛇纹石型红土镍矿分开釆集和处理而 提取镍、 钴、 或者镍和钴的方法。 属于湿法冶金领域。 [1] The present invention relates to a method for extracting nickel and/or cobalt, and in particular to a method for extracting nickel and/or cobalt from laterite nickel ore, in particular by using limonite type and serpentine type laterite A method in which nickel ore is separately collected and treated to extract nickel, cobalt, or nickel and cobalt. It belongs to the field of hydrometallurgy.
背景技术 Background technique
[2] 根据现有技术, 从红土镍矿中提取镍、 钴、 或者镍和钴的方法包括红土镍矿的 堆浸工艺和常压加温搅拌浸取工艺。 [2] According to the prior art, a method for extracting nickel, cobalt, or nickel and cobalt from laterite nickel ore includes a heap leaching process of laterite nickel ore and a normal pressure agitation leaching process.
[3] 然而, 在现有的堆浸工艺中, 将蛇纹石型矿石和褐铁矿型矿石都混在一起进行 堆浸, 结果, 渗透速度慢、 浸取周期长。 [3] However, in the existing heap leaching process, the serpentine type ore and the limonite type ore are mixed together for heap leaching, and as a result, the permeation speed is slow and the leaching period is long.
[4] 另外, 在现有的常压加温搅拌浸取工艺中, 将本可用堆浸工艺也能获得较短浸 取周期的蛇纹石型矿石也与堆浸工艺无法获得较短浸取周期的褐铁矿型矿石混 在一起加温搅拌浸出, 从而导致处理量太大, 使用设备多, 能耗高。 [4] In addition, in the existing atmospheric pressure heating and stirring leaching process, the serpentine type ore which can obtain the shorter leaching period by the available heap leaching process can not obtain the shorter leaching process with the heap leaching process. The periodic limonite-type ore is mixed and heated and stirred for leaching, resulting in too much processing capacity, high use of equipment, and high energy consumption.
对发明的公开 Disclosure of invention
发明内容 Summary of the invention
[5] 为克服现有技术的不足, 本发明的目的是提供一种提取镍和 /或钴的方法, 其 浸取速度快、 浸出周期短、 工艺流程短。 [5] In order to overcome the deficiencies of the prior art, it is an object of the present invention to provide a method for extracting nickel and/or cobalt which has a high leaching speed, a short leaching period, and a short process flow.
[6] 本发明的另外一个目的是提供一种提取镍和 /或钴的方法, 其釆用的设备简单[6] Another object of the present invention is to provide a method for extracting nickel and/or cobalt, which is simple in equipment
、 数量少、 投资小。 , small quantity and small investment.
[7] 本发明的另外一个目的是提供一种提取镍和 /或钴的方法, 其能耗低, 成本效 益好。 [7] Another object of the present invention is to provide a method of extracting nickel and/or cobalt which is low in energy consumption and cost effective.
[8] 本发明的另外一个目的是提供一种提取镍和 /或钴的方法, 其镍浸出率高。 [8] Another object of the present invention is to provide a method of extracting nickel and/or cobalt which has a high nickel leaching rate.
[9] 为此, 本发明提供了一种提取镍和 /或钴的方法, 包括堆浸工艺和常压加温搅 拌浸取工艺, 其特征在于, 褐铁矿型矿石釆用常压搅拌浸取; 而蛇纹石型矿石 釆用堆浸法浸取。 [9] To this end, the present invention provides a method for extracting nickel and/or cobalt, comprising a heap leaching process and a normal pressure heating and stirring leaching process, characterized in that the limonite type ore is cooled by atmospheric pressure stirring. Take; and the serpentine type ore is leached by heap leaching.
[10] 优选地, 从红土镍矿中提取镍和钴、 以及镍或钴。 优选地, 褐铁矿型矿石的常压搅拌浸取工艺包括下列工艺步骤: [10] Preferably, nickel and cobalt, and nickel or cobalt are extracted from laterite nickel ore. Preferably, the atmospheric pressure agitation leaching process of the limonite type ore comprises the following process steps:
控制矿石粒度小于 lcm; Control the ore particle size to be less than lcm;
按矿石 /浸矿剂 (W/V)为 1.0: 1.5 ~ According to ore / leaching agent (W / V) is 1.0: 1.5 ~
1.0:2.5加入浓度为 20~30%的浸矿剂, 在温度为 70~100°C下搅拌浸取 48〜4h; 以 及 1.0:2.5 Adding a leaching agent with a concentration of 20~30%, and immersing for 48~4h at a temperature of 70~100 °C;
将浸出矿浆过滤, 并用水洗涤滤渣, 所得浸出液用于制取镍钴产品。 The leached slurry is filtered, and the filter residue is washed with water, and the resulting leaching solution is used to prepare a nickel-cobalt product.
优选地, 蛇纹石型矿石的堆浸法浸取工艺包括下列工艺步骤: Preferably, the heap leaching process of the serpentine type ore comprises the following process steps:
控制矿石粒度小于 3cm, 控制矿石水份大于 20% ; 矿层厚度为 l~6m; Control the ore particle size to be less than 3cm, control the ore water content to be greater than 20%; the thickness of the ore layer is l~6m;
加入浓度为 5~15%的浸矿剂, 让其自然从上部流入底部进行渗浸; 以及 对收集的浸出液进行调配, 使浸出液镍离子浓度达到 1.5~5g/L, 用于制取镍钴 产品, 镍离子浓度小于 1.2g/L的浸出液返回浸矿。 Adding leaching agent with a concentration of 5~15%, let it naturally infiltrate from the upper part into the bottom; and formulating the collected leachate to make the nickel ion concentration of the leachate reach 1.5~5g/L, for preparing nickel-cobalt products The leachate with a nickel ion concentration of less than 1.2 g/L is returned to the leaching.
优选地, 在步骤 E中, 从浸矿柱顶部加入浓度为 5~15%的浸矿剂, 让其自然从 顶部流入底部进行渗浸。 Preferably, in step E, a leaching agent having a concentration of 5 to 15% is added from the top of the immersion column, and naturally flows into the bottom from the top for infiltration.
优选地, 浸矿剂为含硫酸、 盐酸、 或者它们的混合酸的水溶液。 Preferably, the leaching agent is an aqueous solution containing sulfuric acid, hydrochloric acid, or a mixed acid thereof.
优选地, 用所获得的浸出液制取镍钴产品。 Preferably, the nickel-cobalt product is obtained from the obtained leachate.
优选地, 通过将矿石进行破碎控制矿石粒度。 Preferably, the ore particle size is controlled by crushing the ore.
优选地, 将粒度大于 lcm的矿石进行破碎, 控制矿石粒度小于 lcm; 按矿石 /浸 矿齐 |J(W/V)为 1.0: Preferably, the ore having a particle size larger than lcm is crushed to control the ore particle size to be less than 1 cm; and the ore/immersion ore |J(W/V) is 1.0:
2.3加入 20%的硫酸溶液, 在 80°C下搅拌浸取 24h; 将浸出矿浆过滤, 按液固比为 3加水洗涤滤渣, 浸出液用于制取镍钴产品。 2.3 Add 20% sulfuric acid solution, and immerse for 24h at 80 °C; filter the leaching slurry, wash the filter residue according to the liquid-solid ratio of 3 plus water, and use the leaching solution to prepare nickel-cobalt product.
优选地, 对粒径大于 3cm的矿石进行破碎, 控制矿石粒径小于 3cm, 矿石水份 2 5%; 矿层厚度 5m; 按浸矿剂浓度为 10%配制硫酸水溶液, 矿层顶部加入浸矿剂 , 让其自然渗浸; 分段收集浸出液, 镍钴高峰液集中在浸矿前期, 将浸出液进 行调配, 使浸出液镍离子浓度达到 2g/L, 用于制取镍钴产品, 镍离子浓度小于 1. 2g/L的浸出液用于返回浸矿。 Preferably, the ore having a particle diameter of more than 3 cm is crushed, the ore particle size is less than 3 cm, the ore water content is 25%; the ore layer thickness is 5 m; the sulfuric acid aqueous solution is prepared according to the leaching agent concentration of 10%, and the leaching agent is added to the top of the ore layer. Let it be naturally infiltrated; collect the leachate in sections, concentrate the nickel-cobalt peak in the early stage of leaching, and mix the leachate to make the nickel ion concentration of the leachate reach 2g/L, for the nickel-cobalt product, the nickel ion concentration is less than 1. A 2 g/L leachate was used to return the leach.
根据本发明, 将红土镍矿中的蛇纹石型矿石分釆分浸, 以获得较短的浸出周期 和高的浸出率, 而对剩下的褐铁矿型矿石釆用常压加温搅拌浸出, 使得既有较 [26] 根据本发明, 将红土镍矿中蛇纹石型矿石和褐铁矿型矿石分别釆取不同的浸出 工艺, 蛇纹石型矿石釆取堆浸工艺, 以获得较快的浸取速度, 褐铁矿型矿石釆 用常压加温搅拌工艺浸出, 避免了堆浸速度极慢、 浸取周期长的问题。 According to the present invention, the serpentine-type ore in the laterite nickel ore is distilled to obtain a shorter leaching period and a high leaching rate, and the remaining limonite-type ore is heated and stirred at normal pressure. Leaching, making it easier [26] According to the present invention, the serpentine type ore and the limonite type ore in the laterite nickel ore are respectively subjected to different leaching processes, and the serpentine type ore is subjected to a heap leaching process to obtain a faster leaching speed. The limonite type ore is leached by the atmospheric pressure heating and stirring process, thereby avoiding the problem that the heap leaching speed is extremely slow and the leaching period is long.
[27] 由于蛇纹石型矿石的浸取性能好于褐铁矿型矿石, 相对于现有将上述两种矿石 混合在一起堆浸或搅拌浸取的工艺而言, 本发明将较适合堆浸的蛇纹石型矿石 用堆浸方法浸取, 不仅周期短, 而且浸取率高。 而难于浸取的褐铁矿型矿石用 加温搅拌方法浸取, 不仅浸取速度快, 而且浸取率也高。 因而, 这样的组合工 艺比单一的堆浸工艺或单一的加温搅拌浸取工艺都有更好的技术效果。 附图说明 [27] Since the leaching performance of the serpentine type ore is better than that of the limonite type ore, the present invention is more suitable for the heap than the existing process of mixing the above two ores together for heap leaching or agitation leaching. The immersed serpentine ore is leached by a heap leaching method, which has a short cycle and a high leaching rate. The limonite type ore which is difficult to be leached is leached by the heating and stirring method, and the leaching rate is high, and the leaching rate is also high. Thus, such a combination process has better technical effects than a single heap leaching process or a single warming agitation leaching process. DRAWINGS
[28] 图 1是由褐铁矿型矿石制取镍钴产品的常压搅拌浸取工艺流程图。 [28] Figure 1 is a flow chart of atmospheric pressure stirring leaching process for preparing nickel-cobalt products from limonite ore.
[29] 图 2是由蛇纹石型矿石制取镍钴产品的柱浸 (模拟堆浸) 工艺流程图。 [29] Figure 2 is a flow chart of column immersion (simulated heap leaching) for the preparation of nickel-cobalt products from serpentine ore.
本发明的最佳实施方式 BEST MODE FOR CARRYING OUT THE INVENTION
[30] 本发明人发现, 在堆浸工艺中, 蛇纹石型矿石具有较短的浸取周期; 而褐铁矿 型矿石具有较长的浸取周期。 [30] The inventors have found that serpentine-type ores have a shorter leaching period in the heap leaching process, while limonite-type ores have a longer leaching period.
[31] 如图 1所示, 由褐铁矿型矿石制取镍钴产品的常压搅拌浸取工艺流程包括下列 步骤: 矿石制备步骤 11、 常压搅拌浸取步骤 12、 和固 /液分离步骤 13, 其中, 步 骤 12的实施包括无机酸的施加步骤 111, 固 /液分离步骤 13的结果是产生制取镍钴 产品的浸出液 14和浸出渣 15。 [31] As shown in Fig. 1, the atmospheric pressure stirring leaching process for preparing nickel-cobalt products from limonite ore includes the following steps: ore preparation step 11, atmospheric pressure stirring leaching step 12, and solid/liquid separation Step 13, wherein the step 12 is performed by the inorganic acid application step 111, and the solid/liquid separation step 13 results in the production of the leachate 14 and the leach residue 15 for the nickel-cobalt product.
[32] 在由褐铁矿型矿石制取镍钴产品的常压搅拌浸取工艺的一个实施例中, 具体包 括下列步骤: [32] In one embodiment of the atmospheric agitation leaching process for producing a nickel-cobalt product from a limonite-type ore, the following steps are specifically included:
[33] A、 将粒度大于 lcm的矿石进行破碎, 控制矿石粒度小于 lcm; [33] A, crushing ore with a particle size larger than lcm, controlling the ore particle size to be less than lcm;
[34] B、 按矿石 /浸矿剂 (W/V)为 1.0 : [34] B, by ore / leaching agent (W / V) is 1.0:
2.3加入 20%的硫酸溶液, 在 80°C下搅拌浸取 24h; 2.3 adding 20% sulfuric acid solution, stirring at 80 ° C for 24 h;
[35] C、 将浸出矿浆过滤, 按液固比为 3加水洗涤滤渣, 浸出液用于制取镍钴产品。 [35] C. The leaching slurry is filtered, and the filter residue is washed with a liquid-solid ratio of 3 plus water, and the leaching solution is used for preparing a nickel-cobalt product.
[36] 在本实施例中, 镍浸出率为 82.37% ; 并且可用现有技术处理含镍钴的浸出液, 得镍钴产品。 [36] In the present embodiment, the nickel leaching rate is 82.37%; and the nickel-cobalt-containing leachate can be treated by the prior art to obtain a nickel-cobalt product.
[37] 在其他的实施例中, 矿石 /浸矿剂 (W/V)可以为 1.0: 1.5 ~ 1.0: 2.5, [37] In other embodiments, the ore/leaching agent (W/V) may be 1.0: 1.5 ~ 1.0: 2.5,
浸矿剂的浓度可以为 20 ~30%, 搅拌温度可以为 70 ~ 100°C, 浸取吋间可以为 48〜4h, 同样可以实现本发明的目的。 The concentration of the leaching agent can be 20 ~ 30%, and the stirring temperature can be 70 ~ 100 °C. The leaching time can be 48 to 4 hours, and the object of the present invention can be achieved as well.
[38] 如图 2所示, 由蛇纹石型矿石制取镍钴产品的柱浸法 (模拟堆浸)浸取工艺流程包 括下列步骤: 矿石制备步骤 21、 柱浸 (模拟堆浸) 步骤 22、 浸出夜密度判断步 骤 23, 其中, 柱浸 (模拟堆浸) 步骤 22的实施包括无机酸的施加步骤 211, 结果 是产生制取镍钴产品的浸出液 24和浸出渣 25。 [38] As shown in Fig. 2, the column leaching method (simulation heap leaching) leaching process for preparing nickel-cobalt products from serpentine ore includes the following steps: ore preparation step 21, column leaching (simulation heap leaching) steps 22. Leaching Night Density Judging Step 23 , wherein the column immersion (simulation heap leaching) step 22 comprises the inorganic acid application step 211, with the result that the leaching solution 24 and the leaching slag 25 for producing the nickel-cobalt product are produced.
[39] 在由蛇纹石型矿石制取镍钴产品的柱浸法 (模拟堆浸)浸取工艺一个实施例中, 具体包括下列步骤: [39] In one embodiment of a column leaching method (simulation heap leaching) leaching process for preparing a nickel-cobalt product from a serpentine type ore, the following steps are specifically included:
[40] A、 对粒径大于 3cm的矿石进行破碎, 控制矿石粒径小于 3cm, 矿石水份 25%左 右; [40] A. The ore with a particle size larger than 3cm is broken, the ore particle size is less than 3cm, and the ore water is about 25%;
[41] B、 料层厚度 5m; [41] B, material layer thickness 5m;
[42] C、 按浸矿剂浓度为 10%配制硫酸水溶液, 矿层顶部加入浸矿剂, 让其自然渗 浸; [42] C. Prepare a sulfuric acid aqueous solution at a concentration of 10% of the leaching agent, and add a leaching agent to the top of the ore layer to allow natural infiltration;
[43] D、 分段收集浸出液, 镍钴高峰液集中在浸矿前期, 将浸出液进行调配, 使浸 出液镍离子浓度达到 2g/L, 用于制取镍钴产品, 镍离子浓度小于 1.2g/L的浸出液 用于返回浸矿。 [43] D. Collect the leachate in sections. The nickel-cobalt peak solution is concentrated in the early stage of leaching. The leachate is prepared to make the nickel ion concentration of the leachate reach 2g/L, which is used to prepare nickel-cobalt product. The nickel ion concentration is less than 1.2g/ The leachate of L is used to return the leach.
[44] 在本实施例中, 经过 38天的浸取, 镍浸出率为 84.9%。 并且可用现有技术处理 含镍钴的浸出液, 得镍钴产品。 [44] In this example, after 38 days of leaching, the nickel leaching rate was 84.9%. The nickel-cobalt-containing leachate can be treated by the prior art to obtain a nickel-cobalt product.
[45] 在其他的实施例中, 可控制矿石水份大于 20%; 料层厚度可以为 l~6m, 浸矿剂 的浓度可以为 5~15%, 浸出液镍离子浓度可以为 1.5~5g/L, 同样可以实现本发明 的目的。 [45] In other embodiments, the ore water content may be controlled to be greater than 20%; the material layer thickness may be 1 to 6 m, the concentration of the leaching agent may be 5 to 15%, and the leachate nickel ion concentration may be 1.5 to 5 g/ L, the object of the invention can also be achieved.
[46] 特别是, 在各实施例中, 浸矿剂为含硫酸、 盐酸、 或者它们的混合酸的水溶液 [46] In particular, in each of the examples, the leaching agent is an aqueous solution containing sulfuric acid, hydrochloric acid, or a mixed acid thereof.
[47] 需要指出, 通过以上的公幵内容, 在受到本发明的启发之后, 本领域的技术人 员可能作出这样或那样的修改、 变更、 完善, 然而, 这些都已经包含在权利要 求书的保护范围之内。 [47] It should be noted that, through the above disclosure, those skilled in the art may make such modifications, changes, and improvements after being inspired by the present invention. However, these are all included in the protection of the claims. Within the scope.
Claims
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09737668.5A EP2270241A4 (en) | 2008-04-30 | 2009-04-21 | A method of extracting ni and/or co |
| AU2009242827A AU2009242827B2 (en) | 2008-04-30 | 2009-04-21 | A method of extracting Ni and/or Co |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200810094423 CN101270417B (en) | 2008-04-30 | 2008-04-30 | Method for extracting nickel and/or cobalt |
| CN200810094423.9 | 2008-04-30 |
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| WO2009132558A1 true WO2009132558A1 (en) | 2009-11-05 |
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| PCT/CN2009/071388 Ceased WO2009132558A1 (en) | 2008-04-30 | 2009-04-21 | A method of extracting ni and/or co |
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| EP (1) | EP2270241A4 (en) |
| CN (1) | CN101270417B (en) |
| AU (1) | AU2009242827B2 (en) |
| WO (1) | WO2009132558A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2444574C1 (en) * | 2010-08-20 | 2012-03-10 | Открытое акционерное общество "Кольская горно-металлургическая компания" | Method for obtaining cobalt and its compounds |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101270417B (en) * | 2008-04-30 | 2010-11-03 | 江西稀有稀土金属钨业集团有限公司 | Method for extracting nickel and/or cobalt |
| CN101439314B (en) * | 2008-12-29 | 2013-01-16 | 江西稀有稀土金属钨业集团有限公司 | Ore concentration technique for laterite nickel ore rich in nickel and/or cobalt |
| JP5279938B1 (en) * | 2011-11-09 | 2013-09-04 | 国立大学法人九州大学 | Valuable metal extractant and method for extracting valuable metal using the extractant |
| CN102921538B (en) * | 2012-11-07 | 2013-11-06 | 牛庆君 | Method for recovering and using nickel from serpentine asbestos rock type asbestos gangue |
| CN103614571A (en) * | 2013-10-09 | 2014-03-05 | 北京矿冶研究总院 | Combined leaching process of laterite-nickel ore |
| CN103773951A (en) * | 2014-01-21 | 2014-05-07 | 江苏仁欣化工股份有限公司 | Method for recovering nickel and cobalt through leaching laterite-nickel ore by using sulfuric and hydrochloric acid containing mixed waste acid |
| CN111961879A (en) * | 2020-08-20 | 2020-11-20 | 湖南中伟新能源科技有限公司 | Method for synergistically leaching cobalt sulfide and cobaltosic oxide, preparation method of nickel-cobalt-manganese ternary precursor and preparation method of cobalt |
| CN113088723B (en) * | 2021-04-06 | 2023-04-11 | 吴家明 | Method and system for smelting laterite-nickel ore |
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| CN101301869B (en) * | 2008-04-28 | 2011-08-24 | 三一重工股份有限公司 | Concrete pump vehicle supporting leg and concrete pump vehicle therewith |
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2008
- 2008-04-30 CN CN 200810094423 patent/CN101270417B/en not_active Expired - Fee Related
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2009
- 2009-04-21 AU AU2009242827A patent/AU2009242827B2/en not_active Ceased
- 2009-04-21 EP EP09737668.5A patent/EP2270241A4/en not_active Withdrawn
- 2009-04-21 WO PCT/CN2009/071388 patent/WO2009132558A1/en not_active Ceased
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Also Published As
| Publication number | Publication date |
|---|---|
| EP2270241A4 (en) | 2016-07-13 |
| EP2270241A1 (en) | 2011-01-05 |
| AU2009242827B2 (en) | 2014-05-08 |
| CN101270417B (en) | 2010-11-03 |
| AU2009242827A1 (en) | 2009-11-05 |
| CN101270417A (en) | 2008-09-24 |
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