Easy-to-disperse acrylate-coated zinc stearate composite material and preparation thereof
A technology of composite materials and zinc stearate, which is applied in the field of modified zinc stearate materials and its preparation, can solve problems such as reducing interfacial compatibility, and achieve the effects of low cost, increased application range, and excellent stability
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Embodiment 1
[0035] (1) Mix 5 g of commercially available zinc stearate, 0.008 g of silane coupling agent KH-570 and 75 g of ethanol in a beaker, stir magnetically for 10 min, add 2.5 g of aqueous polyacrylate solution, stir magnetically for 10 min, and disperse ultrasonically for 20 min ;
[0036] (2) Add 5 g of sodium hydroxide solution with a mass fraction of 25% into the mixed solution, and stir magnetically at 25° C. for 15 min.
[0037] (3) The mixed solution was filtered, and the white precipitate was collected, and fully washed with deionized water until neutral.
[0038] (4) The collected product was dispersed in 15 g of deionized water, ultrasonically dispersed for 30 min; pre-frozen at -80° C., dried by a lyophilizer, and collected.
[0039] figure 1 The flow chart of the product process.
Embodiment 2
[0041] (1) Mix 5 g of commercially available zinc stearate, 0.008 g of silane coupling agent KH-570 and 75 g of ethanol in a beaker, stir magnetically for 10 min, add 5.0 g of aqueous polyacrylate solution, stir magnetically for 10 min, and disperse ultrasonically for 20 min ;
[0042] (2) Add 5 g of sodium hydroxide solution with a mass fraction of 25% into the mixed solution, and stir magnetically at 25° C. for 15 min.
[0043] (3) The mixed solution was filtered, and the white precipitate was collected, and fully washed with deionized water until neutral.
[0044](4) The collected product was dispersed in 15 g of deionized water, ultrasonically dispersed for 30 min; pre-frozen at -80° C., dried by a lyophilizer, and collected.
[0045] Such as figure 2 In , the contact angle of the product decreases, indicating that it has a certain degree of hydrophobicity; image 3 In the infrared spectrum, except for the characteristic peak of zinc stearate, at 1728cm -1 The stretch...
Embodiment 3
[0047] (1) Mix 5 g of commercially available zinc stearate, 0.008 g of silane coupling agent KH-570 and 75 g of ethanol in a beaker, stir magnetically for 10 min, add 7.5 g of aqueous polyacrylate solution, stir magnetically for 10 min, and disperse ultrasonically for 20 min ;
[0048] (2) Add 5 g of sodium hydroxide solution with a mass fraction of 25% into the mixed solution, and stir magnetically at 25° C. for 15 min.
[0049] (3) The mixed solution was filtered, and the white precipitate was collected, and fully washed with deionized water until neutral.
[0050] (4) The collected product was dispersed in 15 g of deionized water, ultrasonically dispersed for 30 min; pre-frozen at -80° C., dried by a lyophilizer, and collected.
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