AU2005281684A1

AU2005281684A1 - Preparation of zinc chemicals from the minor flow of a process

Info

Publication number: AU2005281684A1
Application number: AU2005281684A
Authority: AU
Inventors: Mikko Ruonala
Original assignee: Outokumpu Technology Oyj
Current assignee: Metso Corp
Priority date: 2004-09-08
Filing date: 2005-09-06
Publication date: 2006-03-16
Also published as: FI117139B; US20070253878A1; CA2577863A1; EA010853B1; FI20041163A0; CN100406593C; CN101014723A; PE20060757A1; MX2007002750A; EP1794334A1; WO2006027412A1; FI20041163L; EA200700420A1; JP2008512569A

Description

WO 2006/027412 PCT/FI2005/000380 Preparation of zinc chemicals from the minor flow of a process The invention relates to the preparation processes of zinc and zinc chemicals. To be more precise, the invention relates to a process arrangement and circuit 5 for preparing zinc chemicals in connection with a hydrometallurgical purification and preparation process of zinc. In connection with zinc preparation, primary and secondary preparations are often mentioned. The primary production refers to various dissolutions of zinc 10 ores, zinc concentrates and calcines and the treatment of solutions obtained therefrom by means of various hydrometallurgical methods, including liquid liquid extraction. The secondary production refers to the use of various raw ma terials of lesser volumes, such as particulates of electric furnaces, Waeltz ox ides and galvanizing cinders, as raw material. 15 In the primary production of zinc, traditional original materials, such as sulphide zinc ores, are concentrated, i.e., a zinc concentrate, and when so desired, also zinc calcine are further prepared from them. Further, a concentrated zinc sul phate solution is often produced from the zinc concentrate and the zinc calcine, 20 being well-suited for the electrolytic preparation of zinc metal. The present in vention relates to the traditional hydrometallurgical primary production of zinc. In the traditional hydrometallurgical production of zinc, complex solution purifi cation is needed after the dissolution of the raw material, comprising the prepa 25 ration of a pure zinciferous solution. The electrolytic preparation of zinc is very sensitive to certain impurity agents. Therefore, it is important to prepare a suffi ciently pure solution for the zinc electrolysis. For the preparation of zinc, a method is widely used, wherein zinc concentrate 30 is calcined to form zinc oxide, the zinc oxide is dissolved in a diluted sulphuric acid solution in a so-called neutral dissolution, the zinciferous solution is puri fied, and zinc is separated from the purified solution by electrolytic separation.

WO 2006/027412 PCT/FI2005/000380 2 At the dissolving stage of the zinc calcine, the zinc dissolves and the major part of the iron contained by the zinc calcine can be separated as zinc ferrite that does not dissolve in the diluted acid. In addition to the zinc, the solution ob 5 tained from the neutral dissolution contains bivalent iron, cadmium, copper, co balt, nickel, calcium, manganese and chlorides. To obtain a solution that is suitable for the electrolytic recovery of zinc, the solu tion obtained from the neutral dissolution is purified by a multi-stage solution 10 purification process. Normally, the solution purification comprises three stages, wherein copper, cobalt, nickel, and finally, cadmium are removed. The zinciferous sulphate solution obtained from the neutral dissolution is also suitable for a feed material in the leaching method of zinc. Until recently, the 15 liquid-liquid extraction has been used for zinc preparation mainly in small-scale processes that employ secondary raw materials. The US Patent 5,135,652, for example, describes a solvent extraction that can be used to selectively sepa rate zinc from the zinc sulphate solution, which may contain zinc sulphate up to its saturation concentration, and one or more of a group containing the follow 20 ing: bivalent iron, trivalent iron, calcium, magnesium, manganese, sodium, po tassium, arsenic, antimony, copper, cadmium, germanium, and indium. The purpose of this invention is to provide a new kind of a process arrangement for producing pure zinc chemicals from the minor flow of a zinc preparation 25 process of a calcining-dissolving-electrolysis type. The invention is based on the fact that part of the production of the zinc sulphate-containing solution ob tained from the dissolving of the calcining-dissolving-electrolysis plant is di rected to the preparation of zinc chemicals. As only part of the production of the zinc sulphate solution is directed to the preparation of zinc chemicals, the ac 30 tual recovery process of zinc that is based on the electrolysis is not disturbed. In the process arrangement according to the invention, the preparation process of zinc chemicals is based on a selective separation of zinc by extraction with WO 2006/027412 PCT/FI2005/000380 3 known extraction techniques. The known extraction process is based on the use of any organically substituted phosphoric acid or organically substituted thiophosphinic acid. According to the invention, the extraction process is con nected to the calcining-dissolving-electrolysis process described above. 5 The invention provides considerable advantages. In the conventional calcining dissolving-electrolysis process, the bottleneck of the production lies in the elec trolysis process. Accordingly, the solution according to the invention for taking the minor flow to the preparation line of zinc chemicals adds value to the actual 10 production process of zinc. The invention provides an advantageous process solution for the preparation of zinc chemicals of a lesser demand. In the extrac tion process of zinc used in the invention, a strong acid solution is generated as a by-product, which can simply be recycled to be exploited in the preparation process of zinc. In that case, no separate investments for the final treatment of 15 the acid solution are needed. The invention comprises a process circuit and arrangement for preparing pure zinc chemicals from a zinc sulphate-containing solution by an extraction method, whereby the raw material flow of the extraction is separated as a minor 20 flow from the calcining-dissolving-electrolysis type process line of zinc primary production after the neutral dissolving stage. Fig. 1 shows a simplified process chart of the calcining-dissolving-electrolysis type preparation process of zinc and the preparation stage of zinc chemicals 25 connected thereto. In the following, the invention is described in detail with reference to the ap pended drawing. 30 In the preparation of zinc, a calcine 10 containing zinc oxide is dissolved in a sulphuric-acid solution in a neutral dissolution. The neutral dissolution is typi cally carried out in several stages. A solution residue 12, which is not soluble in WO 2006/027412 PCT/FI2005/000380 4 the dissolution and contains iron, among others, is directed to a strong acid dis solution. A zinc sulphate-containing solution 11 is directed to a multi-stage solu tion purification, wherein a zinc powder 14 is used to precipitate copper, cobalt, nickel and cadmium. The.solution-purified zinc sulphate solution 15 is directed 5 to an electrolysis plant, wherein the zinc is recovered at cathodes 16 by means of electrolysis. The electrolyte, from which the zinc was recovered 17, contains a considerable amount of sulphuric acid, which is reintroduced by directing it to the strong acid dissolution, among others. In the strong acid dissolution, the acid is used up in reactions. Accordingly, in addition to the recycled acid, a cer 10 tain amount of pure acid is added into the process. In the neutral dissolution, the pH of the solution should not be raised too high. It is reasonable to adjust the pH of the neutral dissolution with fresh acid and, in addition, with an acid 18 that is obtained from the strong acid dissolution. 15 According to the invention, a minor flow 13 is separated from the main flow 11 of the zinc sulphate-containing solution obtained from the neutral dissolution, and directed to the extraction of zinc. In the extraction, diethylhexylphosphoric acid (DEHPA) or di-2-ethylhexylphosphoric acid (D2EHPA) is exploited. To wards the end of the dissolving stage, the pH of the solution that is going to the 20 extraction can be raised to a level suitable for the extraction, when needed, by means of the calcine. Zinc is separated from the organic phase by stripping it with an acid-containing solution 21. The raffinate 19, which is generated in the extraction, contains sulphuric acid, among others, and is directed to the strong acid stage to be reused. 25 In stripping, wherein pure acid is used, the pure zinc can be recovered in a sul phuric-acid solution, wherein the content of zinc can be up to 150g/l. Various pure zinc products can be prepared from this solution 20 by any known meth ods, such as by chemical precipitation or evaporation. 30

Claims

1. A process circuit for preparing pure zinc chemicals from a zinc sul 5 phate-containing solution by means of an extraction method, charac terized in that the raw material flow of the extraction is separated as a minor flow (13) from the calcining-dissolving-electrolysis type of a process line (11) of the zinc primary production after a neutral dissolu tion stage. 10

2. A process arrangement according to Claim 1, characterized in that a raffinate (19) that is generated in the extraction is directed to be re used in the strong acid dissolution of the said calcining-dissolving electrolysis type of a process. 15

3. A process arrangement according to Claim 1, characterized in that diethylhexylphosphoric acid (DEHPA) or di-2-ethylhexylphosphoric acid (D2EHPA) is exploited in the extraction. 20

4. A process arrangement according to Claim 1, characterized in that towards the end of the dissolving stage, the pH of the solution going to the extraction is raised to a level suitable for the extraction by means of a calcine.