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Preparation method of alkaline battery negative electrode material

A negative electrode material and alkaline battery technology, applied in battery electrodes, circuits, electrical components, etc., can solve the problems of low specific surface area, large particle size, wide particle size distribution, etc., and achieve high specific surface area, low cost and rapid response Effect

Active Publication Date: 2013-11-20
BEIJING INSTITUTE OF TECHNOLOGYGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In view of the problems of large particle size, wide particle size distribution, particle agglomeration and generally low specific surface area of ​​borides in the negative electrode materials of alkaline batteries in the prior art, the purpose of the present invention is to provide a preparation of negative electrode materials for alkaline batteries method

Method used

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  • Preparation method of alkaline battery negative electrode material
  • Preparation method of alkaline battery negative electrode material
  • Preparation method of alkaline battery negative electrode material

Examples

Experimental program
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Effect test

Embodiment 1

[0037] Place the reactor in an environment of 4°C, under the stirring condition of a magnetic stirrer, add 0.1mol / L, 100mL of CoCl 2 The solution was added to the reactor. Then, at a rate of 1 mL / min, add excess NaBH with NaOH to adjust the pH value to 12 dropwise. 4Solution (0.5mol / L, 100mL), continued to stir for 0.5h after the dropwise addition to ensure complete reaction, and precipitate 1 was obtained. The obtained precipitate 1 was washed three times with deionized water and then suction-filtered to obtain precipitate 2. Put the precipitate 2 into a cold trap, drop to -90°C together with the cold trap, and freeze at -90°C for 3 hours at a cooling rate of 15°C / min. After freezing, vacuumize to sublimate the liquid in the sediment 2 to realize the drying process. Under the conditions of vacuum degree ≤ 10.0Pa (the vacuum degree can be maintained at ≤ 10.0Pa under the technical conditions of this experiment, the vacuum degree is constantly changing in the actual experime...

Embodiment 2

[0040] Place the reactor in an environment of 4°C, under the stirring condition of a magnetic stirrer, add 0.1mol / L, 100mL of CoCl 2 The solution was added to the reactor. Then, at a rate of 5 mL / min, add excess NaBH with NaOH to adjust the pH value to 12 dropwise. 4 solution (0.1mol / L, 100mL), continue to stir for 0.5h after the dropwise addition to ensure the completion of the reaction, drive away the hydrogen bubbles, and obtain precipitate 1. The obtained precipitate 1 was washed three times with deionized water and then suction-filtered to obtain precipitate 2. Put the precipitate 2 into a cold trap, drop to -90°C together with the cold trap, and freeze at -90°C for 3 hours at a cooling rate of 15°C / min. After freezing, vacuumize to sublimate the liquid in the sediment 2 to realize the drying process. Under the conditions of vacuum degree ≤ 10.0Pa (the vacuum degree can be kept at ≤ 10.0Pa under the technical conditions of this experiment, the vacuum degree is constant...

Embodiment 3

[0043] Place the reactor in an environment of -8°C, under the stirring condition of a magnetic stirrer, add 0.1mol / L, 100mL of CoCl 2 The solution was added to the reactor. Then, at a rate of 5 mL / min, add excess NaBH with ammonia water to adjust the pH value to 12 dropwise. 4 solution (0.5mol / L, 100mL), continue to stir for 0.5h after the dropwise addition to ensure the completion of the reaction, drive away the hydrogen bubbles, and obtain precipitate 1. The obtained precipitate 1 was washed three times with absolute ethanol and once with deionized water, and then suction-filtered to obtain precipitate 2, which was placed in a refrigerator at -4°C for 1 hour. The temperature of the cold trap was lowered to -90°C, and the precipitate 2 placed in the -4°C refrigerator for 1 hour was put into the cold trap, and frozen at -90°C for 6 hours. After freezing, vacuumize to sublimate the liquid in the sediment 2 to realize the drying process. Under the conditions of vacuum degree ...

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Abstract

The invention discloses a preparation method of an alkaline battery negative electrode material, belonging to the field of energy materials. In the method, a precursor can be obtained through solution chemical reaction and frozening-vacuumizing treatment at a low temperature, and then the precursor is subjected to heat treatment to obtain the alkaline battery negative electrode material, wherein a reactor is placed in the environment of minus 20 DEG C to 4 DEG C, thus the temperature of the reaction system can be lowered and the reaction can be performed in a mild manner. The frozening-vacuumizing treatment at a low temperature can be used to prepare the alkaline battery negative electrode material with high specific surface area and uniform particle size distribution. The preparation method has the advantages of rapid reaction in early stage, simple and convenient process in follow-up stages and strong operability; the negative electrode material prepared by the method is a evenly-dispersed boride and has the advantages of uniform particle size distribution, good dispersibility and high specific surface area.

Description

technical field [0001] The invention relates to a preparation method of an alkaline battery negative electrode material, belonging to the field of energy materials. Background technique [0002] With the continuous improvement of energy and power requirements of power supplies for electrical equipment, the existing alkaline batteries are facing great challenges. Among them, the research on hydrogen storage alloys for Ni / MH battery anode materials mainly focuses on AB 5 Type rare earth alloy, AB 2 Type Laves phase alloy, AB 2 Type magnesium-based alloys, AB-type metal compounds, and vanadium-based solid solution alloys with a body-centered cubic structure. The electrochemical capacity of these alloys is low, and there are problems such as high cost, difficult activation, and serious environmental pollution, which limit the wider application of Ni / MH batteries. [0003] Studies have found that in many boride alloys formed by highly inert transition metals (such as V, Ti, M...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01M4/58
CPCY02E60/12Y02E60/10
Inventor 吴川吴锋庞春会白莹李肖肖陈实杨立伟胡文龙
Owner BEIJING INSTITUTE OF TECHNOLOGYGY