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1,3-dioxane Preparation Method

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1,3-dioxane ring preparation process is concentrated formaldehyde and ethylene glycol with concentrated sulfuric acid as a catalyst in the reactor at 90 ~ 110 ℃ under atmospheric pressure reaction, and then distilled from the top of the distillation column 70 ~ 74 ℃ azeotrope, salted out by sodium chloride, solid alkali drying, re-distillation of the reboil and light bulb after removal of products. If you need to prepare 1,3-dioxetane, you can contact us, we have  1,3-dioxane plant , and easy to operate, safe and reliable.

1,3-dioxane Preparation Process

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The traditional  1,3-dioxetane production process , get the products from paraformaldehyde and ethylene glycol reaction. Paraformaldehyde and ethylene glycol were fed into a reaction kettle at a molar ratio of 1: 1.25, and subjected to atmospheric pressure reaction at 90 to 110°C with a strong acid macroporous cation exchange resin as a catalyst. Then, 70 to 74℃ azeotropes were distilled off from the top of the distillation column, after salting out and dehydrated over anhydrous calcium chloride, followed by distillation and purification, extract 71 ~ 74℃ fractions, make the water off to 200 ppm with molecular sieve, we can get the product.    

The Role of Dioxolane

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The dioxetane is the second monomer of the paraformaldehyde and is copolymerized with the proportion of the paraformaldehyde at a ratio of 95: 5. At the same time, the dioxane is also a good organic solvent and can dissolve the oil, dye, cellulose derivative, a variety of polymers, used for the production of coatings, adhesives; can also be trichloroethane stabilizer, photographic liquid, developer components. In recent years, the application of dioxane in various fields has been expanding. We have  1,3-dioxolane plant  and supply  1,3-dioxolane production process .