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Process for producing taurine drying and sterilizing by microwave and high-efficiency ebullition

A technology of ethylene oxide method, drying and sterilization, which is applied to the preparation of sulfonic acid, chemical instruments and methods, and the preparation of organic compounds. It can solve problems such as unstable product quality, low output, and short drying time, and achieve Reduce the chance of moisture return and agglomeration, reduce the effect of greatly reducing water vapor, and shorten drying time

Inactive Publication Date: 2012-05-09
SHAYANG TIANYI MEDICINE IND
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AI Technical Summary

Problems solved by technology

The advantage of this equipment is that it can guarantee the crystal form to the greatest extent, the production is stable, and there are few affected factors, but this method is labor-intensive and the equipment efficiency is low; 2. Fluidized bed drying and sterilization; adopting fluidized bed drying, The drying time of this method is short, the damage of the crystal form is small, and the water after drying is less, but it is greatly affected by the feed rate and steam pressure, the energy consumption is high, and the loss of materials is large. The biggest problem is that the dried product produced by this method is The quality of the product is unstable and the sterilization effect is poor; 3. Spray granulation drying and sterilization, this method has a large investment, but it is a complete failure in principle and practical application effect. The main problem is that the expanded taurine cannot be guaranteed. The strength of the particles, after being squeezed by their own weight, will become a powder, which is more likely to agglomerate and cannot be cooled quickly in a high temperature state; the oven drying that was added later has been proved by production to be labor-intensive, low-yield, and not suitable for large-scale production. large-scale industrial production
4. High-efficiency boiling drying sterilization method: using GFG high-efficiency boiling dryer for drying, this method occupies a small area, high drying efficiency, low labor intensity, stable quality, very easy to achieve large-scale sterilization, and the effect is also very good The main disadvantage of this method is that the drying time is longer after the traditional bus sterilization method is used. Generally, a single batch of 500-600KG materials is dried, sterilized, and cooled in three stages of about 1.5-2 hours. Time, too long time will lead to a large number of collisions between the crystal and the crystal, between the crystal and the equipment, causing a large area of ​​the crystal form to be broken, resulting in a small crystal form, a lot of powder, and easy agglomeration. This shortcoming is in the long-distance transportation process. The most prominent among them, causing a large area of ​​severe agglomeration and other problems

Method used

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Embodiment Construction

[0013] Sodium bisulfite (45-48%) (20M 3 O) and ion membrane liquid caustic soda (30%) (1.5M 3 ) when the temperature reaches 50-70 DEG C, feed ethylene oxide in the addition kettle, the pressure is normal pressure, the end point is that the pH is greater than 12, and after the number of drops is 3-9 drops, enter the ammonia adjustment process, in the adjustment kettle Internally adjust the ammonia content to 20-21%, sodium hydroxide content to 14%, and adjust the volume to 25M 3 , adjust the temperature at 30-40°C, adjust the pressure below 5KG, after the adjustment,

[0014] Directly pump into the high pressure pump through the booster pump, the flow of the pump is controlled at 8M 3 / H. The pressure is controlled at 18MPa, and the temperature of the material is raised to 200-220°C in 5 sets of casing heaters through an oil bath, and then enters the synthesis tower for synthesis reaction. The flash content is controlled at 18-22%, and the steam plate of the evaporator The...

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Abstract

A processing technology for producing taurine through microwave and high-performance boiling combined dry sterilization ethylene oxide method. The processing technology is characterized in that the processing technology comprises the following steps: the centrifugal wet high-quality product enters into a tunnel microwave drying machine for microwave drying sterilization, wherein, the temperature is controlled to 80-100 DEG C, while the time is controlled to 3-8 minutes; the product then enters into an efficient boiling machine for dry sterilization, with the temperature at 110-130 DEG C and the drying time for 1-1.5 hours. If the drying time for the efficient boiling dry sterilization is shorted, the direct use of efficient boiling sterilization drying time is around 1 hour and 40 minutes. If microwave drying followed by high-performance boiling drying, only one hour is enough. The processing technology has the advantages that the efficient boiling drying sterilization adopts pasteurization; a better effect can be achieved by cross-sterilization through microwave sterilization and efficient boiling drying sterilization. The material has slight caking through microwave, while the caking can be completely broken after efficient boiling drying sterilization to reduce the loss of the materials in the late stage.

Description

technical field [0001] The invention relates to the field of pharmaceutical processing technology. Specifically relate to the processing technique of taurine. Background technique [0002] Taurine is also called α-aminoethanesulfonic acid. The earliest production of taurine was extracted from bezoar by the extraction method, and the raw materials for this method were extremely rare. The current production process of taurine is chemical synthesis method, mainly ethylene oxide method. The process is: add ethylene oxide, sulfur dioxide, caustic soda, soda ash, liquid ammonia, sulfuric acid, etc. Addition, adjustment and synthesis reactions are carried out in the process, followed by flash evaporation, pre-steaming, evaporation, neutralization and crystallization, pressure filtration, purification, decolorization, fine filtration, centrifugation, drying, crushing, and finally packaged into finished products. The drying process mainly includes: 1. Oven drying and sterilization...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C309/14C07C303/02C07C303/44
Inventor 何长江余启新王华章徐东平
Owner SHAYANG TIANYI MEDICINE IND
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