Colloid electrolyte of storage battery and preparation method thereof
A colloidal electrolyte and battery technology, applied in lead-acid batteries, etc., can solve problems such as low glue filling efficiency, poor battery performance, and difficult glue filling, and achieve the effects of increasing glue filling speed, improving fluency, and improving wettability
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specific Embodiment approach 1
[0013] The accumulator colloidal electrolyte that this specific embodiment provides is made by the following method: Under constant stirring, 2.9g specific surface area is 400m 2 / g gas phase nano-SiO 2 Gradually added to 97.1g dilute sulfuric acid solution with a concentration of 35%, heated up to 50°C and stirred vigorously for 2 hours to obtain colloidal dispersion A; Add ZnO whiskers to dispersion A, continue to stir vigorously for 4 hours, cool down to room temperature, and obtain dispersion B; under stirring conditions, dissolve 1 g of starch, 3 g of sodium sulfate and 4.5 g of phosphoric acid into dispersion B and dissolve until dispersed In liquid B, continue stirring for 1 hour to obtain a colloidal electrolyte with good thixotropic fluidity and gel stability. The viscosity of the control colloid without ZnO whiskers was 1398mPa.s, and the viscosity of the colloid with ZnO whiskers was 174mPa.s.
specific Embodiment approach 2
[0014] The accumulator colloidal electrolyte that this specific embodiment provides is made by the following method: Under constant stirring, 10g specific surface area is 150m 2 / g gas phase nano-SiO 2 Gradually added to 90g of dilute sulfuric acid solution with a concentration of 40%, heated to 50°C and stirred vigorously for 4 hours to obtain 100g of colloidal dispersion A; Needle-shaped MgO whiskers were added to the dispersion A, and continued to stir vigorously for 6 hours, then cooled to room temperature to obtain the dispersion B; under stirring conditions, 1.5g sucrose, 3.5g sodium sulfate, 0.05g cobalt sulfate and 5.0g phosphoric acid Dissolved in dispersion B and continued to stir for 2 hours to obtain a colloidal electrolyte with good thixotropic fluidity and gel stability. The viscosity of the control colloid without MgO whiskers was 2471mPa.s, and the viscosity of the colloid with MgO whiskers was 426mPa.s.
specific Embodiment approach 3
[0015] The battery colloidal electrolyte provided in this specific embodiment is prepared by the following method: 14.9g of the specific surface area is 100m under constant stirring 2 / g gas phase SiO 2 Gradually added to 85.1g dilute sulfuric acid solution with a concentration of 45%, heated to 50°C and stirred vigorously for 8 hours to obtain colloidal dispersion A; Add the glass microfibers into the dispersion A, continue to stir vigorously for 8 hours, cool down to room temperature, and obtain the dispersion B; under stirring conditions, dissolve 3g of glycerol, 5g of sodium sulfate and 6.5g of phosphoric acid into the dispersion B, Stirring was continued for 3 hours to obtain a colloidal electrolyte with good thixotropic fluidity and gel stability. The viscosity of the control colloid without glass microfibers is 3219mPa.s, and the viscosity of the colloid with glass microfibers is 632mPa.s.
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Abstract
Description
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