Method for recovering alkali, selenium and arsenic in arsenic-alkali residue from antimony smelting

A technology of arsenic-alkali slag and arsenic-alkali slag, which is applied in the field of antimony smelting arsenic-alkali slag disposal, selenium and arsenic, and recovery of alkali from arsenic-alkali slag, which can solve the problem of unrealized component recovery, unstable product components, and affecting glass quality and other issues, to achieve good economic and environmental benefits, high utilization, and reduce production costs

Active Publication Date: 2019-08-20
CENT SOUTH UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

For example, the sodium arsenate compound salt method is to recover the antimony in the arsenic-alkali slag by water leaching, concentrate and evaporate the leachate to dryness, and dry the physical water to obtain the sodium arsenate compound salt. This compound salt is still a hazardous solid waste, although it can be used as glass Clarifying agent, but the product components are unstable, which is easy to affect the quality of the glass. Now the environmental protection requirements are stricter, and its use is strictly restricted. At the same time, the sodium arsenate compound salt contains valuable components that can be recycled, and relevant recovery of components
CN 200410013369.2 discloses a method for separating and recovering sodium arsenate and alkali by fractional crystallization. The method uses the difference in solubility between sodium arsenate and sodium carbonate at high temperature to realize the separation and recovery of arsenic and alkali. The o

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0034] Example 1

[0035] The method is used to treat secondary arsenic-alkali slag from an antimony smelter in Hunan, and the water content of the arsenic-alkali slag is 31.2%. Crush the arsenic slag to less than 5mm, then take 1.2 kg of arsenic slag and leaching with water at a liquid-to-solid ratio of 3mL / g, stirring speed 100r / min and leaching temperature of 95℃ for 1h, filter and wash to obtain antimony slag and arsenic alkali Solution. The alkali leaching rate of the arsenic-alkali residue leaching and washing process was 100%, and the leaching rates of As, Sb and Se were 98.4%, 1.8% and 97.9%, respectively. Table 1 shows the content of related components in arsenic-base slag and antimony slag (dry basis), and Table 2 shows the content of related components in arsenic-base solution.

[0036] Table 1 Contents of related components of arsenic-alkali slag and antimony slag (%)

[0037]

[0038] Table 2 Contents of relevant components in arsenic alkali solution (g / L)

[0039]

Example Embodiment

[0049] Example 2

[0050] The experimental conditions of the arsenic slag, arsenic slag leaching and washing, and the twice recovery of alkali with carbon dioxide used in this example are the same as in Example 1. Adjust the pH of the secondary crystallization mother liquor to 2.9 with sulfuric acid, heat it to 100°C for 20 minutes, and filter while it is hot to obtain black selenium and de-selenium liquid. The direct yield of selenium is 81.3%. The content of related components in black selenium is shown in Table 4. Show. CO produced during pH adjustment by sulfuric acid 2 Return to the alkali recovery process for recycling.

[0051] After removing selenium, the solution is fed with SO at 25℃ and stirring speed 200r / min 2 Reducing As(V) to As(III), then concentrating the reduced liquid by 3.8 times, then cooling and crystallizing at 25℃, and filtering to obtain crude arsenic trioxide and the liquid after arsenic removal. The direct arsenic yield is 80.7%. After arsenic removal Th

Example Embodiment

[0054] Example 3

[0055] The method is used to treat the secondary arsenic-alkali slag from an antimony smelter in Hunan, and the water content of the arsenic-alkali slag is 29.1%. The arsenic slag is crushed to below 5mm, and then 1.2kg of arsenic slag is leached with water at a liquid-solid ratio of 3.5mL / g, stirring speed 100r / min and leaching temperature 105℃ for 1h, filtered and washed to obtain antimony slag and arsenic alkali Solution. The leaching rate of arsenic-alkali residue in the leaching and washing process was 100%, and the leaching rates of As, Sb and Se were 99.4%, 2.1% and 98.9%, respectively. Table 5 shows the content of related components in arsenic-base slag and antimony slag (dry basis), and Table 6 shows the content of related components in arsenic-base solution.

[0056] Table 5 Contents of related components of arsenic-alkali slag and antimony slag (%)

[0057]

[0058] Table 6 Contents of relevant components in arsenic-alkali mixture (g / L)

[0059]

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Abstract

The invention discloses a method for recovering alkali, selenium and arsenic in arsenic-alkali residue from antimony smelting, comprising the following steps: (1) immersing arsenic-alkali residue in water, filtering and washing to obtain antimony slag and an arsenic-alkali solution; (2) concentrating the arsenic-alkali solution until concentration of arsenic is 12-17 g/L, introducing CO2 to obtainsodium hydrogen carbonate and primary crystallization mother liquor, concentrating the primary crystallization mother liquor until concentration of arsenic is 48-60 g/L, and introducing CO2 to obtainsodium hydrogen carbonate and secondary crystallization mother liquor; (3) using acid to regulate pH of the secondary crystallization mother liquor to 1-4, heating and reacting to obtain black selenium and a selenium-removed solution; and (4) carrying out SO2 reduction on the selenium-removed solution, conducting evaporation and concentration, cooling for crystallization and filtering to obtain arsenic trioxide and an arsenic-removed solution. By the above method, efficient recovery of alkali, selenium and arsenic in arsenic-alkali residue is realized, and effective enrichment of antimony isalso realized, oxidation for deep antimony removal is not required, arsenic-alkali separation is thorough, no sodium arsenate composite salt is generated, and acid consumption and use amount of a reducing agent are low. In addition, the process is concise, and the method has good economic and environmental benefits.

Description

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Claims

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Application Information

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Owner CENT SOUTH UNIV
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