Method for directly recovering lead oxide used for a lead-acid battery cathode from waste lead paste

Patent metadata

Field	Value
Publication number	US-9828654-B2
Application number	US-201414906452-A
Country	US
Kind code	B2
Filing date	May 27, 2014
Priority date	Feb 21, 2014
Publication date	Nov 28, 2017
Grant date	Nov 28, 2017

Abstract

Provided is a method for directly recovering lead oxide used for a lead-acid battery negative electrode from waste lead paste. The method comprises: (1) contacting waste lead paste with a barium-containing desulphurizer under desulphurization reaction conditions, and performing a solid-liquid separation on the mixture after contacting to obtain a filtrate and a filtration residue; and (2) performing a conversion reaction on the above-mentioned filtration residue at a temperature of 350-750° C. so as to convert the lead-containing components in the filtration residue into lead oxide. In the method, the direct recovery of a lead oxide raw material applicable to a lead-acid battery negative electrode from waste lead paste is achieved by quantitatively replenishing a barium sulphate additive in the process of desulphuration thereby substantially decreasing the recovery cost and energy consumption, and improving the comprehensive utilization of waste lead paste.

First claim

The invention claimed is:

1. A method for directly recovering lead oxide for negative electrode of lead-acid battery from waste lead paste, comprising the following steps:
(1) controlling waste lead paste to contact with a barium-containing desulfurizing agent to desulfurize through wet ball milling, and carrying out solid-liquid separation for a mixture obtained from the contact, to obtain filtrate and filter residue;
(2) controlling the filter residue to have a conversion reaction at 350-750° C., to convert lead-containing components in the filter residue into lead oxide, thereby obtaining a product of lead oxide and barium sulfate;
wherein the barium-containing desulfurizing agent is NaOH and/or KOH solution containing soluble barium compound and/or barium sulfate and the concentration of the NaOH and/or KOH solution is 4-23 wt %.

2. The method according to claim 1 , wherein based on the total weight of the barium-containing desulfurizing agent, the content of the soluble barium compound and/or barium sulfate is 0.001-15 wt %.

3. The method according to claim 1 , wherein the soluble barium compound is one or more of barium hydroxide, barium nitrate, barium perchlorate, barium chloride, and barium acetate.

4. The method according to claim 1 , wherein the conversion reaction in step (2) is carried out in the presence of a promoter, which is added in step (1) and/or step (2).

5. The method according to claim 4 , wherein the promoter is selected from the group consisting of lead powder, barium powder, aluminum powder, sodium powder, lithium powder, potassium powder, magnesium powder, nickel powder, tin powder, stibium powder, zinc powder, naphthalene, camphor, urea, carbon powder, active carbon containing 0.5-95 wt % PbO, and a mixture of the above-mentioned substances with β-lead peroxide mixed at any mix ratio.

6. The method according to claim 4 , wherein the dosage of the promoter is 0.05-30 wt % of the filter residue obtained in step (1).

7. The method according to claim 1 , further comprising: supplementing the barium-containing desulfurizing agent into the filtrate obtained in step (1), and controlling the concentration of the barium-containing desulfurizing agent in the obtained filtrate to 90-150% of the concentration before the contact.

8. The method according to claim 1 , further comprising: cooling product obtained in step (2) to 100-300° C. within during a period of 0.5-30 min following the completion of step (2).

9. The method according to claim 8 , wherein the cooling is implemented by means of liquid mist cooling, and the coolant is one or more of water, methanol, ethanol, and acetone.

10. The method according to claim 1 , wherein the contact between the waste lead paste and the barium-containing desulfurizing agent is implemented by means of a wet ball milling and mixing process.

11. The method according to claim 10 , wherein the ball milling conditions include: based on 1,000 g waste lead paste, the mass of the balls is 5-500 g, the number of the balls is 5-100, the ball milling time is 0.1-200 min, and the temperature is −5° C. to 105° C.

12. The method according to claim 4 , further comprising: supplementing the barium-containing desulfurizing agent into the filtrate obtained in step (1), and controlling the concentration of the barium-containing desulfurizing agent in the obtained filtrate to 90-150% of the concentration before the contact.

13. The method according to claim 8 , wherein cooling the product obtained in step (2) to 100-150° C. during a period of 1-10 min following the completion of step (2).

14. The method according to claim 13 , wherein the cooling is implemented by means of liquid mist cooling, and the coolant is one or more of water, methanol, ethanol, and acetone.

Assignees

• Chilwee Power Co Ltd
• Univ Beijing Chem Tech
• Chilwee Power Co Ltd & Beijing Univ Of Chemical Technology

Inventors

• Pan Junqing
• Ma Yongquan
• Sun Yanzhi
• Cai Xiaoxiang
• Niu Yinjian
• Liu Xiaowei
• Song Shuang
• Chen Tixian
• Cao Guoqing
• Zhou Mingming
• Yang Xinxin
• Zhou Longrui
• Yang Yunfei

Classifications

• Y02W30/84

  Recycling of batteries or fuel cells · CPC title

• Y02P10/234

  Cross-Sectional Technologies · mapped topic

• H01M10/54

  Reclaiming serviceable parts of waste accumulators · CPC title

• C22B7/006

  Wet processes · CPC title

• C22B13/045 Primary

  Recovery from waste materials · CPC title