C22 triacid triester plasticizer and preparation method thereof
A technology of ester plasticizer and acid three, which is applied in the field of plasticizers, can solve the problems of high biodegradability and plasticizing ability, and cannot meet the non-toxicity of plasticizers, so as to improve utilization rate, reduce production cost, The effect of shortening the reaction time
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Embodiment 1
[0050] C 22 Trimethyl triacid plasticizer preparation
[0051] (1) Preparation of Methyl Caryonate
[0052] In a 500ml three-necked flask equipped with a constant temperature oil bath, a stirring device, a thermometer, and a reflux condenser, add 298g of tung oil, heat to 120°C, dehydrate under reduced pressure for 1-2h, make the water content less than 0.2%, cool to 50°C, add 260g methanol, 5g potassium hydroxide, react at 60-70°C for 4h, recover excess methanol, and cool to room temperature. Glycerin was separated, and after washing with water to remove the catalyst, free water and excess methanol were distilled off to obtain 280 g of methyl lyceate.
[0053] (2) Synthesis of dimethyl maleate
[0054] In a 500mL three-necked flask equipped with a constant temperature oil bath, stirring device, thermometer, and fractional distillation condenser, add 200g of maleic anhydride, 250g of methanol and 4.5g of [HSO 3 -bmim] + [HSO 4 ] - , carry out the esterification reaction...
Embodiment 2
[0058] C 22 Preparation of Dibutyl Methyl Triate Plasticizer
[0059] (1) Preparation of Methyl Caryonate
[0060] In a 500ml three-necked flask equipped with a constant temperature oil bath, a stirring device, a thermometer, and a reflux condenser, add 298g of tung oil, heat to 120°C, dehydrate under reduced pressure for 1-2h, make the water content less than 0.2%, cool to 50°C, add 260g methanol, 5g potassium hydroxide, react at 60-70°C for 4h, recover excess methanol, and cool to room temperature. Glycerin was separated, and after washing with water to remove the catalyst, free water and excess methanol were distilled off to obtain 280 g of methyl lyceate.
[0061] (2) Synthesis of dibutyl maleate
[0062] In a 500mL three-neck flask equipped with a constant temperature oil bath, stirring device, thermometer, and fractional distillation condenser, add 200g of maleic anhydride, 400g of butanol and 6g of [HSO 3 -bmim] + [HSO 4 ] - , carry out the esterification reactio...
Embodiment 3
[0066] C 22 Preparation of tributyl triacid plasticizer
[0067] (1) Preparation of butyl sulphonate
[0068] In a 500ml three-necked flask equipped with a constant temperature oil bath, a stirring device, a thermometer, and a reflux condenser, add 298g of tung oil, heat to 120°C, dehydrate under reduced pressure for 1-2h, make the water content less than 0.2%, cool to 50°C, add 360g butanol, 8g potassium hydroxide, react at 80-100°C for 4h, recover excess butanol, and cool to room temperature. Glycerin was separated, and after washing with water to remove the catalyst, free water and excess butanol were distilled off to obtain 320 g of butyl sulphonate.
[0069] (2) Synthesis of dibutyl maleate
[0070] In a 500mL three-neck flask equipped with a constant temperature oil bath, stirring device, thermometer, and fractional distillation condenser, add 200g of maleic anhydride, 400g of butanol and 6g of [HSO 3 -bmim] + [HSO 4 ] - , carry out the esterification reaction at ...
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