Method for preparing high-substitution hydrobutyl starch through acid-base synergy pretreatment
A technology of hydroxybutyl and high substitution, which is applied in the field of acid-base synergistic pretreatment to prepare high-substituted hydroxybutyl starch, which achieves the effects of high reaction efficiency, improved reaction efficiency and simple equipment
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Embodiment 1
[0072] 1) Disperse the waxy cornstarch in ethanol, configure the starch milk with a mass fraction of 30%, and place it in a three-necked flask. Stir well at room temperature, add concentrated hydrochloric acid with starch dry basis weight of 1.4mL / g, and stir for 0.3h. The water bath was warmed up to 50°C and stirred for 3h. Stop heating, neutralize with sodium carbonate solution to pH 6.8, wash the obtained product with ethanol / water (50v / v), and dry in an oven at 45°C for 24h to obtain acid pretreated waxy cornstarch.
[0073] 2) Take acid pretreated waxy cornstarch and disperse it in ethanol to prepare starch milk with a mass fraction of 10%, and put it in a three-necked flask. In a water bath at 40°C, add an alkali solution containing 0.06% of sodium hydroxide on a dry basis of starch dropwise at a uniform speed, and react for 50 minutes. The obtained product was neutralized to pH 6.8 with 10% by mass fraction of dilute hydrochloric acid, washed with ethanol / water (50v / v...
Embodiment 2
[0079]1) Disperse cornstarch in methanol, configure starch milk with a mass fraction of 35%, and place it in a three-necked flask. Stir well at room temperature, add concentrated hydrochloric acid with a starch dry basis weight of 1.7mL / g, and stir for 0.3h. The water bath was warmed up to 45°C and stirred for 4h. Stop heating, neutralize with sodium carbonate solution to pH 6.8, wash the obtained product with ethanol / water (70v / v), and dry in an oven at 45°C for 24h to obtain acid pretreated cornstarch.
[0080] 2) Disperse acid-pretreated cornstarch in ethanol to prepare starch milk with a mass fraction of 10%, and place it in a three-necked flask. In a water bath at 40°C, add an alkali solution containing 0.04% of sodium hydroxide on a dry basis of starch dropwise at a uniform speed, and react for 45 minutes. The obtained product was neutralized to pH 6.8 with 8% mass fraction of dilute hydrochloric acid, washed with 95% ethanol, and dried in an oven at 45°C for 24 hours ...
Embodiment 3
[0083] 1) Disperse potato starch in isopropanol, configure starch milk with a mass fraction of 35%, and place it in a three-necked flask. Stir evenly at room temperature, add concentrated hydrochloric acid with a dry weight of starch of 2 mL / g, and stir for 40 min. The water bath was warmed up to 45°C and stirred for 5h. Stop heating, neutralize to pH 6.8 with sodium carbonate solution, wash the obtained product with ethanol / water (60v / v), and dry in an oven at 45°C for 24h to obtain acid pretreated potato starch.
[0084] 2) Take acid pretreated potato starch and disperse it in isopropanol to prepare starch milk with a mass fraction of 12% in a three-necked flask. In a water bath at 40°C, add an alkali solution containing 0.05% by mass of sodium hydroxide on a starch dry basis dropwise at a uniform speed, and react for 50 minutes. The obtained product was neutralized with 8% dilute hydrochloric acid to a pH of 6.8, washed with 95% ethanol, and dried in an oven at 45°C for 2...
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