阅读说明：本技术 一种净化锌矿物料浸出液的方法 (Method for purifying zinc mineral material leaching solution ) 是由 汪胜东 张登高 张登凯 赵峰 胡凯 王海北 周科华 李达 郑莉莉 蒋训雄 徐克华 于 2020-11-05 设计创作，主要内容包括：一种净化锌矿物料浸出液的方法,属于湿法炼锌技术领域,依次包括以下步骤：(1)将锌矿物料浸出液用锌矿焙砂中和,液固分离。(2)将中和后的浸出液加入含有单质锌的物料,置换铜、镓、锗等有价元素,液固分离；含有单质锌的物料优选步骤(4)的高温净化渣。(3)将置换后的浸出液经针铁矿法除铁,液固分离。(4)将除铁后的浸出液在高温下加入锌粉、锑白、硫酸铜,进行除镍、钴,液固分离,得到除镍、钴后的浸出液和高温净化渣。(5)将除镍、钴后的浸出液在低温下再加入锌粉,进行除镉,得到合格的硫酸锌电解前液。本发明有助于锌冶炼企业显著降低净化渣种类和产出量,有利于后续低成本综合回收其中有价金属,可大大提高企业经济效益。(A method for purifying zinc mineral material leaching solution belongs to the technical field of zinc hydrometallurgy, and sequentially comprises the following steps: (1) neutralizing the zinc mineral leaching solution with zinc ore calcine, and carrying out liquid-solid separation. (2) Adding the neutralized leachate into a material containing simple substance zinc, replacing valuable elements such as copper, gallium, germanium and the like, and carrying out liquid-solid separation; the material containing the simple substance zinc is preferably the high-temperature purification slag in the step (4). (3) And removing iron from the replaced leachate by a goethite method, and carrying out liquid-solid separation. (4) Adding zinc powder, antimony white and copper sulfate into the leachate after iron removal at high temperature, removing nickel and cobalt, and performing liquid-solid separation to obtain the leachate after nickel and cobalt removal and high-temperature purification slag. (5) And adding zinc powder into the leaching solution after nickel and cobalt removal at low temperature to remove cadmium, thereby obtaining qualified zinc sulfate pre-electrolysis solution. The method is beneficial to remarkably reducing the types and the output of the purified slag for zinc smelting enterprises, is beneficial to comprehensively recovering valuable metals in the purified slag at low cost, and can greatly improve the economic benefit of the enterprises.)

1. A method for purifying zinc mineral material leaching solution is characterized by sequentially comprising the following steps:

(1) neutralizing the zinc mineral material leaching solution with zinc ore calcine, and carrying out liquid-solid separation;

(2) adding the leachate neutralized in the step (1) into a material containing simple substance zinc, replacing valuable metals, and carrying out liquid-solid separation to obtain a replaced leachate and replacement slag;

(3) removing iron from the leachate obtained by the replacement in the step (2), and carrying out liquid-solid separation to obtain the leachate and iron slag after iron removal;

(4) adding zinc powder, antimony white and copper sulfate into the leachate after iron removal in the step (3) at high temperature, removing nickel and cobalt, and performing liquid-solid separation to obtain the leachate after nickel and cobalt removal and high-temperature purification slag;

(5) and (4) adding zinc powder into the leaching solution after nickel and cobalt removal in the step (4) at low temperature, and simultaneously adding or not adding copper sulfate to remove cadmium and perform liquid-solid separation to obtain qualified zinc sulfate pre-electrolysis solution and low-temperature purification slag.

2. The method according to claim 1, wherein the material containing the elemental zinc in the step (2) is the high-temperature purified slag obtained in the step (4).

3. The method of claim 1, wherein the zinc mineral matter leach solution is a zinc concentrate oxygen pressure leach solution.

4. The method according to claim 1, wherein the sulphuric acid content of the leachate after neutralisation in step (1) is between 1 and 8 g/L.

5. The method of claim 1, wherein the elemental zinc-containing material of step (2) is added in an amount of: the added simple substance zinc is 1 to 10 times of the theoretical consumption of the replacement metal; the replacement temperature is 40-90 ℃, the replacement time is 0.5-3h, and the pH value of the solution is 2-3.

6. The method of claim 1, wherein the iron removal in step (3) is goethite iron removal.

7. The method according to claim 1, wherein the iron content of the leachate after iron removal in step (3) is below 20 mg/L.

8. The method as claimed in claim 1, wherein the zinc powder in the step (4) is added in an amount of 0.8 to 3 times the theoretical consumption of the replacement metal, antimony white is added in an amount of 0.1 to 20mg per liter of the solution, copper sulfate is added in an amount of 1 to 200mg, the purging temperature is 70 to 98 ℃, the purging time is 0.5 to 6 hours, and the solution pH is 4 to 5.

9. The method as claimed in claim 1, wherein the zinc powder in step (5) is added in an amount of 1 to 5 times the theoretical consumption of the replacement metal, copper sulfate is added in an amount of 0 to 100mg per liter of solution, the purging temperature is 30 to 70 ℃, and the purging time is 0.5 to 4 hours.

Technical Field

The invention belongs to the technical field of zinc hydrometallurgy, and relates to a method for purifying zinc mineral material leachate, in particular to a method for purifying zinc concentrate oxygen pressure leachate.

Background

The zinc ore treatment process can be divided into a pyrogenic process and a wet process. The fire method has long process history and mature process, but has high energy consumption, needs equipment for recovering furnace ash and purifying gas, and has high requirement on the equipment. The wet process has relatively low energy consumption, easy automation and mechanization of production, relative environmental protection, but long and complex process flow. The wet process has the advantages of large production scale, low energy consumption, high comprehensive recovery rate of valuable metals, relatively good labor conditions, easy realization of mechanization and automation and the like, and the wet zinc smelting is still the mainstream direction of the zinc smelting technology in the future.

After the zinc concentrate is subjected to acid leaching, elements such as zinc, copper, cadmium, gallium, germanium, nickel, cobalt and the like enter the solution, and in order to meet the subsequent zinc electrodeposition requirement, harmful impurities such as copper, cadmium, gallium, germanium and the like in the leaching solution need to be purified to be below the allowable content. The purification degree of the leaching solution not only directly determines whether the final electrodeposition can be normally carried out, but also determines various technical and economic indexes and final product quality in the electrodeposition process, so that the selection of the purification process is a key part of the zinc hydrometallurgy.

The zinc mineral leaching solution process mainly comprises the steps of purifying and removing iron, copper and cadmium, nickel and cobalt and removing reverse dissolved cadmium.

One method for purifying and removing iron in domestic zinc hydrometallurgy is to precipitate iron in the form of ferric hydroxide by adjusting the pH value of a solution, and at the moment, rare and dispersive elements such as antimony, germanium and the like also form coprecipitation with the ferric hydroxide to precipitate from the solution; the method has the advantages that the zinc can be recovered and the dissipated elements can be enriched simultaneously through the pyrogenic process volatilization process, so that convenience is provided for the subsequent recovery of the dissipated elements; the defects are that the flow is long, a large amount of coke particles are needed to be used as a reducing agent and a part of heat sources, and the production cost is high. The other method is that the pH value of the solution is adjusted after oxidation, ammonia salt and the like are added to precipitate iron in the form of jarosite slag, and the scattered elements are still precipitated together with jarosite, but the leached slag is not treated any more, so that the loss of the scattered elements is caused.

The technology for removing copper and cadmium and removing reverse dissolved cadmium is mature, and a zinc powder replacement method is adopted, so that the consumption of zinc powder is low.

The domestic methods for removing cobalt and nickel can be divided into three types: a method for removing cobalt from xanthate; a cobalt (nickel) removing method by arsenic salt; the method for removing cobalt (nickel) from antimony salt. The method for removing cobalt from xanthate is one of the earliest applied technologies in China, and has the advantages of good cobalt removal effect and lower reaction temperature; the disadvantages are that the xanthate is pungent and has heavy peculiar smell, and the capacity of removing other impurities is weak, thus not being widely popularized and applied. The method for removing cobalt (nickel) from arsenic salt has the advantages of being suitable for removing cobalt when the cobalt content of the solution is high and having wide application; the disadvantages are that arsenic salt is extremely toxic and causes harm to human body during operation. Compared with the two methods, the cobalt (nickel) removing method by using the antimonate has no peculiar smell and toxic or side effect in the operation process, removes impurity elements such as nickel and the like with similar properties to the cobalt while removing the cobalt, and can also remove scattered impurity elements such as arsenic, antimony, germanium and the like, and the deep purification effect is very good.

At present, although the existing research and process have made certain progress, from the domestic zinc sulfate solution purification technology, the purification purity has no problem, and impurities such as iron, copper, cadmium, gallium, germanium, cobalt, nickel and the like can be removed to meet the solution purification requirements required in the electrolytic process. The biggest problems at present are that the consumption of zinc powder is large, the types of purification slag are various, the grade is low, and the comprehensive recovery of valuable elements in the subsequent slag is not facilitated.

Disclosure of Invention

The invention aims to overcome the defects in the prior art, and provides a method for purifying zinc mineral material leachate, namely a method for neutralizing zinc mineral material leachate, returning high-temperature purification slag to replace and enrich gallium and germanium, removing iron by a goethite method, removing nickel and cobalt by high-temperature purification, and removing cadmium by low-temperature purification, which is beneficial to remarkably reducing the types and output of the purification slag of zinc smelting enterprises and is beneficial to the subsequent low-cost comprehensive recovery of valuable metals. Wherein the high-temperature section purification slag contains 40-50% of zinc and 3-8% of cadmium; 1-5% of copper; the cobalt content is less than 0.1 percent, and the zinc powder can reduce the usage amount of the zinc powder and the types of the purification slag while returning to replace and enrich gallium and germanium. The method has the advantages of short flow, simple process, zinc powder consumption saving, high purification depth, contribution to comprehensive recovery of valuable elements and the like, can realize deep purification of a system and internal circulation of local cross-working procedures, and greatly improves the economic benefit of enterprises.

The purpose of the invention is realized by the following technical scheme.

A method for purifying zinc mineral material leaching solution is characterized by sequentially comprising the following steps:

(1) neutralizing the zinc mineral leaching solution with zinc ore calcine, and carrying out liquid-solid separation.

(2) Adding the leachate neutralized in the step (1) into a material containing simple substance zinc, and replacing valuable elements such as copper, gallium, germanium and the like; and (4) carrying out liquid-solid separation to obtain the replaced leachate and the replaced slag. The material containing the simple substance zinc is preferably the high-temperature purification slag obtained in the step (4).

(3) And (3) removing iron from the leachate obtained after the replacement in the step (2), and carrying out liquid-solid separation to obtain the leachate and iron slag after iron removal.

(4) Adding zinc powder, antimony white and copper sulfate into the leachate after iron removal in the step (3) at high temperature, removing nickel and cobalt, and performing liquid-solid separation to obtain the leachate after nickel and cobalt removal and high-temperature purification slag;

(5) and (4) adding zinc powder into the leaching solution after nickel and cobalt removal in the step (4) at low temperature, and simultaneously adding or not adding copper sulfate to remove cadmium and perform liquid-solid separation to obtain qualified zinc sulfate pre-electrolysis solution and low-temperature purification slag.

Further, the zinc ore material leaching solution is zinc concentrate oxygen pressure leaching solution.

Further, the sulfuric acid content of the leachate after neutralization in the step (1) is 1-8 g/L.

Further, the adding amount of the material containing the elemental zinc in the step (2) is as follows: the added simple substance zinc is 1 to 10 times of the theoretical consumption of the replacement metal; the replacement temperature is 40-90 ℃, the replacement time is 0.5-3h, and the pH value of the solution is 2-3.

Further, the method for removing iron in the step (3) is goethite method iron removal.

Furthermore, the iron content of the leachate after iron removal in the step (3) is below 20 mg/L.

Furthermore, the adding amount of the zinc powder in the step (4) is 0.8-3 times of the theoretical consumption amount of the replacement metal, the adding amount of antimony white in each liter of solution is 0.1-20mg, the adding amount of copper sulfate is 1-200mg, the purification temperature is 70-98 ℃, the purification time is 0.5-6h, and the pH value of the solution is 4-5.

Furthermore, the adding amount of the zinc powder in the step (5) is 1-5 times of the theoretical consumption amount of the replacement metal, the adding amount of copper sulfate in each liter of solution is 0-100mg, the purification temperature is 30-70 ℃, and the purification time is 0.5-4 h.

The invention aims at solving the problems of increasing slag accumulation amount and bringing dangerous waste management and safety and environmental protection to factories due to difficult clean slag treatment in a purification workshop in a zinc hydrometallurgy process.

After the research of the inventor, the zinc content of the clean slag is found to be: 40-50%, cadmium: 3-8%; copper-containing: 1-5%; cobalt-containing: < 0.1%; the zinc content is high, and the main component is excessive zinc powder during one-time purification. Therefore, the metal zinc of the slag occupies more than half. Based on this, the clean slag is sent to a replacement procedure to remove impurities from the solution before replacement. Controlling the pH value of an outlet at 2-3 to inhibit the dissolution of impurities in the purified slag by regulating the supplement amount of zinc powder in production; secondly, controlling the Cd of the solution after replacement to be less than or equal to 800mg/L can avoid the accumulation and circulation of impurity cadmium in the system. After the purification slag realizes dynamic open-circuit optimization, the unit consumption of the zinc powder is reduced from 84.2 kg/ton zinc sheets per month to 73 kg/ton zinc sheets per month, and the unit consumption of the zinc powder is reduced by 11.2 kg/ton zinc sheets per month.

The invention adopts the secondary utilization of the metal zinc of the clean slag, namely, the clean slag is sent to the replacement procedure to remove impurities from the solution before replacement, thereby achieving the purposes of reducing the zinc powder consumption for replacement and impurity removal and improving the utilization rate of the zinc powder of the clean slag. Meanwhile, the return of the clean slag can also replace zinc powder to make most of the valuable metals of copper, cadmium, gallium and germanium enter the replacement slag through replacement, thereby providing convenience for the recovery of the subsequent valuable metals of copper, cadmium, gallium and germanium. The invention has important significance for saving resources and protecting environment while improving the utilization rate of the whole resources and increasing the enterprise benefit.

Drawings

FIG. 1 is a process flow diagram of the method of the present invention.

Detailed Description

The process of the invention is further illustrated by the following non-limiting examples to assist understanding of the invention and its advantages, but not to limit the scope of the invention. In the embodiment, zinc concentrate pressure leaching liquid is used as a raw material (chemical components are shown in table 1), calcine is added into the zinc concentrate pressure leaching liquid for neutralization, liquid-solid separation is carried out after neutralization is finished, high-temperature replacement slag is added into neutralized supernatant liquid for replacing valuable metals such as copper, gallium and germanium, liquid-solid separation is carried out after replacement is finished, and the replacement slag is sent to recover valuable elements; removing iron from the solution after replacement by goethite method, adding zinc powder, antimony white and copper sulfate to carry out high-temperature purification for removing nickel and cobalt, carrying out liquid-solid separation after reaction is finished, and returning high-temperature purification slag to the replacement section for replacing and removing copper, cadmium, gallium and germanium; and adding zinc powder and copper sulfate into the high-temperature purified liquid to perform low-temperature purification and cadmium removal, and performing liquid-solid separation after the reaction is finished.

TABLE 1 chemical composition (g/L) of leachate from pressure acid leaching of zinc concentrates

Zn

Cu

Cd

Fe

Co

Ni

Ga(mg/L)

Ge(mg/L)

Sulfuric acid g/L

158.3

1.42

0.62

11.16

＜0.005

＜0.005

22.40

21.60

20.8

Example 1

Adding calcine into zinc concentrate oxygen pressure leaching solution for neutralization, wherein the neutralization time is 1h, the sulfuric acid content after neutralization is 1g/L, and performing liquid-solid separation after neutralization is finished; adding high-temperature purification slag into the neutralized supernatant to perform displacement to remove copper, gallium and germanium, wherein the displacement temperature is 60 ℃, the addition amount (calculated by the contained simple substance zinc powder) of the high-temperature purification slag is 3 times of the theoretical amount of the displaced metal, the displacement time is 3 hours, the displacement is finished when the pH value reaches 3, the liquid-solid separation is performed, the copper displacement rate is 99%, the cadmium displacement rate is 86%, the gallium displacement rate is 92% and the germanium displacement rate is 96%; carrying out goethite deironing on the solution after replacement, wherein the concentration of iron ions in the solution after deironing is 10 mg/L; the liquid after iron removal is purified at high temperature, the purification temperature is 85 ℃, the purification time is 2 hours, the using amount of zinc powder is 3 times of the theoretical amount of the replacement metal, 10mg of antimony white and 40mg of copper sulfate are added into each liter of solution, liquid-solid separation is carried out after high-temperature purification is finished, and the cadmium replacement rate, the nickel replacement rate and the cobalt replacement rate are 98 percent and 99 percent respectively after high-temperature purification; and (3) purifying the high-temperature purified solution at low temperature to remove cadmium, wherein the purification temperature is 55 ℃, the purification time is 2h, the amount of zinc powder is 3 times of the theoretical amount of the replacement metal, 20mg of copper sulfate is added into each liter of solution, liquid-solid separation is carried out after the reaction is finished, and the low-temperature purified cadmium replacement rate is 99%.

Example 2

Adding calcine into zinc concentrate oxygen pressure leaching solution for neutralization, wherein the neutralization time is 1h, the sulfuric acid content after neutralization is 3g/L, and performing liquid-solid separation after neutralization is finished; adding high-temperature purification slag into the neutralized supernatant to perform displacement to remove copper, gallium and germanium, wherein the displacement temperature is 80 ℃, the addition amount (calculated by the contained simple substance zinc powder) of the high-temperature purification slag is 5 times of the theoretical amount of the displaced metal, the displacement time is 2h, the displacement is finished when the pH value reaches 2.5, the liquid-solid separation is performed, the copper displacement rate is 99%, the cadmium displacement rate is 90%, the gallium displacement rate is 94% and the germanium displacement rate is 98%; carrying out goethite deironing on the solution after replacement, wherein the concentration of iron ions in the solution after deironing is 12 mg/L; the liquid after iron removal is purified at high temperature, the purification temperature is 70 ℃, the purification time is 3 hours, the using amount of zinc powder is 2 times of the theoretical amount of the replacement metal, 20mg of antimony white and 20mg of copper sulfate are added into each liter of solution, liquid-solid separation is carried out after high-temperature purification is finished, and the cadmium replacement rate, the nickel replacement rate and the cobalt replacement rate are 98 percent and 99 percent respectively after high-temperature purification; and (3) purifying the high-temperature purified solution at low temperature to remove cadmium at 60 ℃ for 2h, wherein the zinc powder amount is 2 times of the theoretical amount of the replacement metal, 10mg of copper sulfate is added into each liter of solution, liquid-solid separation is carried out after the reaction is finished, and the replacement rate of the low-temperature purified cadmium is 99%.

Example 3

Adding calcine into zinc concentrate oxygen pressure leaching solution for neutralization, wherein the neutralization time is 1h, the sulfuric acid content after neutralization is 6g/L, and performing liquid-solid separation after neutralization is finished; adding high-temperature purification slag into the neutralized supernatant to perform displacement to remove copper, gallium and germanium, wherein the displacement temperature is 90 ℃, the addition amount (calculated by the contained simple substance zinc powder) of the high-temperature purification slag is 5 times of the theoretical amount of the displaced metal, the displacement time is 1h, the displacement is finished when the pH value is 2.8, the liquid-solid separation is performed, the copper displacement rate is 99%, the cadmium displacement rate is 72%, the gallium displacement rate is 81% and the germanium displacement rate is 79%; carrying out goethite deironing on the solution after replacement, wherein the concentration of iron ions in the solution after deironing is 15 mg/L; performing high-temperature purification on the liquid after iron removal, wherein the purification temperature is 90 ℃, the purification time is 2.5h, the using amount of zinc powder is 2.5 times of the theoretical amount of the replacement metal, 20mg of antimony white and 20mg of copper sulfate are added into each liter of solution, liquid-solid separation is performed after the high-temperature purification is finished, and the cadmium substitution rate, the nickel substitution rate and the cobalt substitution rate are 95%, 93% and 90% after the high-temperature purification; and (3) purifying the high-temperature purified solution at low temperature to remove cadmium at 40 ℃ for 4h, wherein the zinc powder amount is 5 times of the theoretical amount of the replacement metal, 60mg of copper sulfate is added into each liter of solution, liquid-solid separation is carried out after the reaction is finished, and the replacement rate of the low-temperature purified cadmium is 99%.

Example 4

Adding calcine into zinc concentrate oxygen pressure leaching solution for neutralization, wherein the neutralization time is 1h, the sulfuric acid content after neutralization is 6g/L, and performing liquid-solid separation after neutralization is finished; adding high-temperature purification slag into the neutralized supernatant to perform displacement to remove copper, gallium and germanium, wherein the displacement temperature is 40 ℃, the addition amount of the high-temperature purification slag (calculated by the contained simple substance zinc powder) is 8 times of the theoretical amount of the displaced metal, the displacement time is 1h, the displacement is finished when the pH value is 3, and the liquid-solid separation is performed, wherein the copper displacement rate is 99%, the cadmium displacement rate is 92%, the gallium displacement rate is 91% and the germanium displacement rate is 87%; carrying out goethite deironing on the replaced liquid, wherein the concentration of iron ions in the liquid after deironing is 10 g/L; performing high-temperature purification on the liquid after iron removal, wherein the purification temperature is 98 ℃, the purification time is 2 hours, the using amount of zinc powder is 2 times of the theoretical amount of the replacement metal, 20mg of antimony white and 20mg of copper sulfate are added into each liter of solution, liquid-solid separation is performed after high-temperature purification is finished, and the cadmium replacement rate, the nickel replacement rate and the cobalt replacement rate are 88 percent, 91 percent and 89 percent after high-temperature purification; and (3) purifying the high-temperature purified solution at low temperature to remove cadmium, wherein the purification temperature is 70 ℃, the purification time is 0.5h, the amount of zinc powder is 3 times of the theoretical amount of the replacement metal, 100mg of copper sulfate is added into each liter of solution, liquid-solid separation is carried out after the reaction is finished, and the low-temperature purified cadmium replacement rate is 94%.

Example 5

Adding calcine into zinc concentrate oxygen pressure leaching solution for neutralization, wherein the neutralization time is 1h, the sulfuric acid content after neutralization is 6g/L, and performing liquid-solid separation after neutralization is finished; adding high-temperature purification slag into the neutralized supernatant to perform displacement to remove copper, gallium and germanium, wherein the displacement temperature is 40 ℃, the addition amount of the high-temperature purification slag (calculated by the contained simple substance zinc powder) is 8 times of the theoretical amount of the displaced metal, the displacement time is 1h, the displacement is finished when the pH value is 3, and the liquid-solid separation is performed, wherein the copper displacement rate is 99%, the cadmium displacement rate is 92%, the gallium displacement rate is 91% and the germanium displacement rate is 87%; carrying out goethite deironing on the solution after replacement, wherein the concentration of iron ions in the solution after deironing is 18 mg/L; performing high-temperature purification on the liquid after iron removal, wherein the purification temperature is 70 ℃, the purification time is 2 hours, the using amount of zinc powder is 2 times of the theoretical amount of the replacement metal, 0mg of antimony white and 200mg of copper sulfate are added into each liter of solution, liquid-solid separation is performed after high-temperature purification is finished, and the cadmium substitution rate, the nickel substitution rate and the cobalt substitution rate are 86%, 83% and 80% after high-temperature purification; and (3) purifying the high-temperature purified solution at low temperature to remove cadmium, wherein the purification temperature is 70 ℃, the purification time is 1.5h, the amount of zinc powder is 3 times of the theoretical amount of the replacement metal, 0mg of copper sulfate is added into each liter of solution, liquid-solid separation is carried out after the reaction is finished, and the replacement rate of the low-temperature purified cadmium is 85%.