Microcapsules
A technology of microcapsules and monomers, applied in the direction of microcapsule preparation, microsphere preparation, coating detergent composition, etc., can solve problems such as unmentioned advantages
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Embodiment 1
[0362] Example 1: Preparation of capsules according to the invention (samples 1 to 3)
[0363] The aqueous phase was prepared by dissolving 4.0 g poly(vinyl alcohol) (hydrolyzed to 87-89%, Mw = 85000-124000 g / mol) in 196.0 g water. The oil phase was prepared by mixing 85.0 g of each perfume substance No. 1, 2 and 3, 13.7 g of 1,4-butanediol dimethacrylate, 13.1 g of methacrylic acid and 5.2 g of methyl methacrylate and 0.9 g prepared from lauroyl peroxide. The mixture was stirred until the lauroyl peroxide was completely dissolved.
[0364] The aqueous and oil phases were placed in a 500 mL-bath reactor equipped with a condenser, thermometer, nitrogen inlet and deflocculant plates (4 cm in diameter). During all processes, the mixture was stirred at 900 rpm and nitrogen was purged through the mixture to remove oxygen. First, the mixture was heated from room temperature to 35°C within 20 min and kept at 35°C for 1 hour. The resulting emulsion was then heated to 70°C within 3...
Embodiment 2
[0367] Example 2 (Comparative): Preparation of Capsules Using Crosslinker 1,4-Butanediol Diacrylate (Samples 4 and 5)
[0368] The aqueous phase was prepared by dissolving 4.0 g poly(vinyl alcohol) (hydrolyzed to 87-89%, Mw = 85000-124000 g / mol) in 196.0 g water. The oil phase was prepared by mixing 85.0 g of each fragrance substance No. 1 and 2, 13.7 g of 1,4-butanediol diacrylate, 13.1 g of methacrylic acid and 5.2 g of methyl methacrylate and 0.9 g of lauryl peroxide acyl to prepare. The mixture was stirred until the lauroyl peroxide was completely dissolved.
[0369] The aqueous and oil phases were placed in a 500 mL-bath reactor equipped with a condenser, thermometer, nitrogen inlet and deflocculant plates (4 cm in diameter). During all processes, the mixture was stirred at 900 rpm and nitrogen was purged through the mixture to remove oxygen. First, the mixture was heated from room temperature to 35 °C within 20 min and kept at 35 °C for 1 h. The resulting emulsion wa...
Embodiment 3
[0372] Embodiment 3 (comparison): Use the preparation of the capsule of cross-linking agent pentaerythritol triacrylate (sample 6)
[0373] The aqueous phase was prepared by dissolving 4.0 g poly(vinyl alcohol) (hydrolyzed to 87-89%, Mw = 85000-124000 g / mol) in 196.0 g water. The oil phase was prepared by mixing 85.0 g of each perfume substance No. 1, 2 or 3, 13.7 g of pentaerythritol triacrylate, 13.1 g of methacrylic acid and 5.2 g of methyl methacrylate and 0.9 g of lauroyl peroxide. The mixture was stirred until the lauroyl peroxide was completely dissolved.
[0374] The aqueous and oil phases were placed in a 500 mL-bath reactor equipped with a condenser, thermometer, nitrogen inlet and deflocculant plates (4 cm in diameter). During all processes, the mixture was stirred at 900 rpm and nitrogen was purged through the mixture to remove oxygen. First, the mixture was heated from room temperature to 35 °C within 20 min and kept at 35 °C for 1 h. The resulting emulsion was...
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