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Continuous Ion Exchange Lab Equipment

   Continuous chromatographic separation of experimental equipment ∑uses advanced design concepts and superb production process. It is suitable for a small amount of ÷product preparation and process technology development, wide range of uses It is user-friendly ¶and can be based on different product separation requirements flexible adjustment p∑rocess.

 
   Continuous chromatographic separation principle:

   The chromatographic separation techniqu→e is based on the fact that different materials have differeγnt partition coefficients in the system consisting of stationary phase and mobile ph←ase, and different retention times are presented in the mobile phase elution process to achieve sλeparation. The traditional chromatographic
separation technique is carried out using a fixed chroma≈tographic column. We first enter a certain amount of material, and then use elue≥nt continuous elution. The same exit at different times can receive♦ different product components, the process time and effort. After analysis and im<provement, we made the stationary phase of the resin which can be continuous flow of the system. Th÷e separation of the material and the relative velocity of the stati‌onary phase is achieved. Similar to the principles of the tortoise and the hare ÷we put the fixed phase into a conveyor belt, the rabbit turtle, respectively, comparedδ to the speed of the two different components. As long a×s the stationary phase adds a driving force in the opposite direc÷tion to the elution, so that the speed of the conveyor belt in← the middle of the rabbit and turtle speed. Rabbits run faste↓r than the fixed phase from the front, and the slow turtle was bro ught to the back of the conveyor belt.




   We can use continuous moving bed system to achieve the ‌above process:
 


 


 Continuous chromatographic separation advantages:
 

  •   Integration of all the steps can be continuous operation, the system mat±ching is strong;
  •   Significantly reduce the amount of resin, and give full play to the use of resin potenti₽al;
  •   Extend the service life of the resin;
  •   Reduce water and chemical consumption, and significantly reduce ope↓rating costs and reduce sewage emissions;
  •   Remove or separate substances with different characteristics, which can be comple>x process simplification;
  •   Maintain the stability of the product composition and concentra§tion in the feed liquid;
  •   Effectively improve the purity and concentration of product liquid, saving the cost of fol∑low-up technology;
  •   The use of multi-column system is flexible to change the production proc€ess;
  •   Compact, small footprint, easy to install in any location;
  •   Fully automated, programmed operation control, to ensu♣re continuous and stable operation of the equipment; and
  •   Flexibility to adjust the rotation speed or adju∑st the flow rate according to the process.

 

 Typical applications:
 

  •   Fructose separation production of crystalline fructose;
  •   Separation and Purification of Xylitol and Arabino♦se;
  •   Mannitol and sorbitol separation and purification;
  •   Separation and purification of glucose and galactose;
  •   Separation and purification of arabinose and ribose;
  •   Glucose or maltose and high sugar separation and purifica₩tion;
  •   Maltose and glucose separation and purification;
  •   Isolation of valine and alanine;
  •   Soybean oligosaccharides in the raffinose, stachyose and mono→saccharides, disaccharide separation;
  •   Maltitol and oligosaccharides, sorbitol separation;
  •   Citric acid chromatographic separation;
  •   P-xylene adsorption separation;
  •  Chiral compounds isolated; and
  •   Separation of isomers.


Technical Parameters


 

 


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