Method for preparing isosorbide by sorbitol dehydration
A technology for isosorbide and sorbitol, applied in the field of isosorbide preparation from sorbitol, can solve the problems of harsh catalytic conditions, low isosorbide yield and the like, and achieves the advantages of good thermal stability, high catalytic efficiency and mild reaction conditions. Effect
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Embodiment 1
[0018] Weigh 1g coconut shell activated carbon, 2g p-aminobenzenesulfonic acid and 1g sodium hydroxide into 150ml deionized water and stir thoroughly. After heating to 80℃, add 1g sodium nitrite and 5ml dilute hydrochloric acid (2mol / L ), after reacting for 10 hours, filtering, washing, and drying at 100° C. to remove water in the solid, to obtain the carbon-based catalyst A functionally modified with benzenesulfonic acid groups.
Embodiment 2
[0020] Weigh 1g of mesoporous carbon, 2g of p-aminobenzenesulfonic acid and 1g of potassium hydroxide into 150ml of deionized water and stir thoroughly. After heating to 20℃, add 1g of sodium nitrite and 5ml of dilute hydrochloric acid (2mol / L) to the mixture. After reacting for 10 hours, it is filtered, washed, and dried at 100°C to obtain the carbon-based catalyst B functionally modified with benzenesulfonic acid groups.
Embodiment 3
[0022] Weigh 1g of mesoporous carbon, 4g of p-aminobenzenesulfonic acid and 1g of calcium hydroxide into 150ml of deionized water and stir thoroughly. After heating to 60℃, add 2g of sodium nitrite and 5ml of dilute hydrochloric acid (2mol / L) to the mixture. After reacting for 15 hours, it is filtered, washed, and dried at 100°C to obtain the carbon-based catalyst C functionally modified with benzenesulfonic acid groups.
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