The production method of polyoxymethylene dimethyl ether
A production method and dimethyl ether technology, applied in the field of synthesizing polyoxymethylene dimethyl ether, can solve the problems of high cost and low catalyst reaction efficiency, and achieve the effects of low production cost, increased yield and high reaction conversion rate
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Embodiment 1
[0024] 1. Preparation of catalyst
[0025] (1) Polymerization and hybridization: at room temperature, add 144 grams of styrene, 16 grams of divinylbenzene, 1 gram of BPO and 40 grams of toluene to a 1000 ml three-necked flask and stir evenly, then add 40 grams of 500-mesh zigzag CNTs, and stir Evenly, add 300 grams of 1.0w% PVA aqueous solution, then react at 70°C for 3 hours, 80°C for 1 hour, and 95°C for 45 minutes under stirring to obtain a pellet-shaped product. Stop stirring and keep boiling the pellets at 95°C for 30 minutes. All the products in the three-necked flask were poured into water for cleaning. The product was washed with ethanol and then washed with H 2 O was washed, placed in an oven and dried at 80° C. for 4 h to obtain 200 g of catalyst precursor I.
[0026] (2) Sulfonation: Add 200 grams of catalyst precursor I to 400 grams of 1,2-dichloroethane to swell at room temperature for 4 hours, then add 100 grams of H with a purity of 98w%. 2 SO 4 , stirring a...
Embodiment 2
[0033] 1. Preparation of catalyst
[0034] (1) Polymerization and hybridization: at room temperature, add 144 g of styrene, 16 g of divinylbenzene, 1 g of BPO and 40 g of toluene into a 1000 ml three-neck flask and stir evenly, then add 40 g of 500-mesh armchair-type CNTs, Stir evenly, add 300 grams of 1.0w% PVA aqueous solution, then react at 70°C for 3 hours, 80°C for 1 hour, and 95°C for 45 minutes under stirring to obtain a pellet-shaped product. Stop stirring and keep boiling the pellets at 95°C for 30 minutes. All the products in the three-necked flask were poured into water for cleaning. The product was washed with ethanol and then washed with H 2 O was washed, placed in an oven and dried at 80° C. for 4 h to obtain 200 g of catalyst precursor I.
[0035] (2) Sulfonation: Add 200 grams of catalyst precursor I to 400 grams of 1,2-dichloroethane to swell at room temperature for 4 hours, then add 100 grams of H with a purity of 98w%. 2 SO 4 , stirring and downloading a...
Embodiment 3
[0040] 1. Preparation of catalyst
[0041] (1) Polymerization and hybridization: at room temperature, add 144 grams of styrene, 16 grams of divinylbenzene, 1 gram of BPO and 40 grams of toluene to a 1000 ml three-necked flask and stir evenly, then add 40 grams of 500-mesh helical CNTs, and stir Evenly, add 300 grams of 1.0w% PVA aqueous solution, then react at 70°C for 3 hours, 80°C for 1 hour, and 95°C for 45 minutes under stirring to obtain a pellet-shaped product. Stop stirring and keep boiling the pellets at 95°C for 30 minutes. All the products in the three-necked flask were poured into water for cleaning. The product was washed with ethanol and then washed with H 2 O was washed, placed in an oven and dried at 80° C. for 4 h to obtain 200 g of catalyst precursor I.
[0042] (2) Sulfonation: Add 200 grams of catalyst precursor I to 400 grams of 1,2-dichloroethane to swell at room temperature for 4 hours, then add 100 grams of H with a purity of 98w%. 2 SO 4 , stirring ...
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