Aggregate zeolitic absorbents, their method of preparation and their uses
View Patent ↗The present invention relates to aggregate zeolitic adsorbents based on zeolite X and zeolite LSX. These adsorbents are particularly suitable for separating C 8 aromatic isomers and in particular xylenes, separating sugars, separating polyhydric alcohols, separating isomers of substituted toluenes, separating cresols, separating dichlorobenzenes.
1. An aggregate zeolitic adsorbent comprising:
zeolite X powder exchanged to at least 90% by barium ions alone or by barium ions and potassium ions, the exchangeable sites representing up to ⅓ of the exchangeable sites occupied by the barium plus potassium ions, remaining sites being occupied by alkali or alkaline-earth ions other than barium and potassium,
zeolite LSX powder exchanged to at least 90% by barium ions alone or by barium ions and potassium ions, the exchangeable sites representing up to ⅓ of the exchangeable sites occupied by the barium plus potassium ions, remaining sites being occupied by alkali or alkaline-earth ions other than barium and potassium, wherein the molar ratio of the zeolite LSX concentration to the zeolite X concentration is between 0.1 and 10;
and a binder in a proportion lower than or equal to 20% by weight of the total weight of the aggregate zeolitic adsorbent.
2. The adsorbent as claimed in claim 1 , wherein the molar ratio of the zeolite LSX concentration to the zeolite X concentration is between 0.5 and 2.0.
3. The adsorbent as claimed in claim 1 , wherein the zeolite X essentially consists of crystals having a mean (number) diameter measured by SEM and counting, of between 0.1 and 4 μm.
4. The adsorbent as claimed in claim 1 , wherein the zeolite LSX essentially consists of crystals having a mean (number) diameter measured by SEM and counting, of between 0.1 μm and 7 μm.
5. A method for preparing an adsorbent as claimed in claim 1 , comprising the following steps:
a) agglomeration of a mixture consisting of zeolite LSX powder and zeolite X powder in a LSX/X ratio carrying between 0.1 and 10 with an agglomeration binder, followed by shaping, drying and calcination, and
b) replacement of at least 90% of all the exchangeable sites of the aggregate by barium, followed by washing and drying of the product thus treated.
6. A method for separating C 8 aromatic isomers, sugars, polyhydric alcohols, isomers of substituted toluenes, cresols, or dichlorobenzenes, the method comprising a step of contacting a feed stock with the adsorbent as claimed in claim 1 .
7. A method as claimed in claim 6 , wherein a paraxylene is recovered from aromatic C 8 isomer cuts.
8. The method as claimed in claim 7 , which is carried out in liquid phase.
9. The method as claimed in claim 7 , which is carried out in gas phase.
10. The method for recovering paraxylene as claimed in claim 7 , which is of the simulated moving bed type.
11. The method for recovering paraxylene as claimed in claim 7 , which is of the simulated countercurrent type.
12. The method for recovering paraxylene as claimed in claim 7 , which is of the simulated cocurrent type.
13. The method for recovering paraxylene as claimed in claim 7 , further comprising contacting the absorbent with a desorbent, wherein the desorbent is toluene or paradiethylbenzene.
14. The method for recovering paraxylene, as claimed in claim 7 , wherein the zeolitic adsorbent has an ignition loss measured at 900° C. of between 4.0 and 8%.
15. The adsorbent as claimed in claim 1 , wherein the molar ratio of the zeolite LSX concentration to the zeolite X concentration is between 0.25 and 4.
16. The adsorbent as claimed in claim 1 , wherein the molar ratio of the zeolite LSX concentration to the zeolite X concentration is between 0.54 and 1.86.
17. The adsorbent as claimed in claim 1 , wherein the zeolite X essentially consists of crystals having a mean (number) diameter measured by SEM and counting, of between 1 and 3 μm.
18. The adsorbent as claimed in claim 1 , wherein the zeolite X essentially consists of crystals having a mean (number) diameter measured by SEM and counting, of between 0.1 and 2 μm.
19. The adsorbent as claimed in claim 1 , wherein the zeolite LSX essentially consists of crystals having a mean (number) diameter measured by SEM and counting, of between 0.1 μm and 4 μm.
20. The adsorbent as claimed in claim 1 , wherein the zeolite LSX essentially consists of crystals having a mean (number) diameter measured by SEM and counting, of between 0.1 μm and 3 μm.
21. The adsorbent as claimed in claim 1 , wherein the zeolite LSX essentially consists of crystals having a mean (number) diameter measured by SEM and counting, of between 0.1 μm and 2 μm.
22. The method of claim 5 , wherein the LSX/X ratio is between 0.25 and 4.0.
23. The method of claim 5 wherein the LSX/X ration is between 0.5 and 2.0.
24. The method of claim 5 , wherein at least part of the binder contains one or more zeolitizable clays.
25. The method of claim 24 , wherein the binder contains at least 80% by weight of the one or more zeolitizable clays.
26. The method of claim 22 , further comprising zeolitization of the zeolitizable portion of the binder by the action of a basic alkaline solution, after step a).
27. The method of claim 5 , further comprising replacement of no more than 33% of all the exchangeable sites of the aggregate by potassium, followed by washing and drying of the product thus treated, after step b).
28. The method of claim 27 , further comprising an activation step after the washing and drying of the product.
29. The method of claim 5 , further comprising an activation step, after step b).
30. The method of claim 14 , wherein the zeolitic adsorbent has an ignition loss measured at 900° C. of between 4.7 and 6.7%.
31. The method of claim 6 , wherein the C 8 aromatic isomers are xylenes.