Suspension particle comprising tetrafluoroethylene polymer and manufacturing method thereof
A technology of polymers and granules, which can be used in tableware, applications, coatings, etc., and can solve problems such as complex processes
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Embodiment 1
[0043] 27 kg of styrene, 3 kg of acrylonitrile and 210 g of benzoyl peroxide were introduced into a reaction containing 75 kg of deionized water and 50 kg of L-Teflon (commercially available under the trade name FR 301B; solids content: 60%) container, and stir the mixture. Add 1.2 kg of hydroxyapatite and 80 g of sodium alkylbenzene sulfonate to the stirred mixture and stir at 300 RPM. Polymerization of the compounds was terminated by heating the contents of the reactor to 75°C and maintaining that temperature for 7 hours, then heating to 120°C and maintaining that temperature for 3 hours. The aqueous phase was removed to yield uniform pellets with an average diameter of 1.1 mm. The resulting pellets were dried using a fan air heater.
Embodiment 2
[0045] 27 kg of styrene, 3 kg of acrylonitrile and 210 g of benzoyl peroxide were introduced into a reaction containing 75 kg of deionized water and 50 kg of L-Teflon (commercially available under the trade name FR 301B; solids content: 60%) container, and stir the mixture. 78 g of polyvinyl alcohol (Dongyang steel chemical Co., Ltd.) and 80 g of sodium alkylbenzenesulfonate were added to the stirred mixture and stirred at 400 RPM. Polymerization of the compounds was terminated by heating the contents of the reactor to 75°C and maintaining that temperature for 7 hours, then heating to 120°C and maintaining that temperature for 3 hours. The aqueous phase was removed to yield uniform pellets with an average diameter of 0.8 mm. The resulting pellets were dried using a fan air heater.
Embodiment 3
[0047] 27 kg of styrene, 9 kg of acrylonitrile and 210 g of benzoyl peroxide were introduced into a reaction containing 75 kg of deionized water and 50 kg of L-Teflon (commercially available under the trade name FR 301B; solids content: 60%) container, and stir the mixture. Add 1.2 kg of hydroxyapatite and 80 g of sodium alkylbenzene sulfonate to the stirring mixture and stir at 300 RPM. Polymerization of the compounds was terminated by heating the contents of the reactor to 75°C and maintaining that temperature for 7 hours, then heating to 120°C and maintaining that temperature for 3 hours. The aqueous phase was removed to yield uniform pellets with an average diameter of 1.8 mm. The resulting pellets were dried using a fan air heater.
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