Tunable adsorbents

Patent metadata

Field	Value
Publication number	US-11529582-B2
Application number	US-202016880324-A
Country	US
Kind code	B2
Filing date	May 21, 2020
Priority date	Feb 13, 2017
Publication date	Dec 20, 2022
Grant date	Dec 20, 2022

Abstract

The present invention relates to a method for modifying the crystalline inorganic framework of an adsorbent with coatings to provide rate selectivity for one gas over others is described. The method described herein narrows the effective pore size of crystalline porous solids with pores less than about 5 Å for rate selective separations. This method of the invention comprises treating the hydrated or partially hydrated zeolite with a silicone derived binding agent followed by subsequent heat treatment. The additive content and treatment are adjusted to match effective pore size to specific separations. The superior adsorbent has the added convenience of bead forming simultaneously with pore modification as well as having the treatment result in the yielding of high crush strength products.

First claim

We claim:

1. A surface modified A-type zeolite adsorbent having a starting effective pore size of less than or equal to 4.1 Å wherein the starting pore size of said zeolite is reduced by 0.1 up to about 1.2 Å with a coating comprised of a silicone derived species, wherein said species is derived from a silicone precursor of formula I:
[( R ) 2 SiO] n
or of formula II:
R SiO 1.5

wherein each R substituent is the same or different and is selected from a substituted or unsubstituted organic compound.

2. The adsorbent of claim 1 wherein said adsorbent is shaped into agglomerates, beads, extrudates, or pellets.

3. The adsorbent of claim 1 wherein said A-type zeolite is exchanged with one or more cations selected from Li, Na, K, Mg, Ca, Sr, Ba, Ag, Cu, or Zn.

4. The adsorbent of claim 1 wherein each R is the same or different and is selected from H, straight, branched or cyclic, substituted or unsubstituted, C 1 to C 8 alkyl, alkenyl, alkynyl, alkoxy and aryl.

5. The adsorbent of claim 1 wherein each R is the same or different and is selected from linear, branched and cyclic compounds C 1 to C 4 organic compounds.

6. The adsorbent of claim 1 wherein the silicone precursor is polymeric or oligomeric and each R is independently terminated by hydroxy, methoxy, ethoxy or combinations thereof.

7. The adsorbent of claim 1 wherein the silicone precursor is selected from hydroxy, methoxy, or ethoxy terminated polymeric di-methylsiloxane, methyl-silsesquioxanes, octyl-silsesquioxanes, methyl octyl-silsesquioxanes or combinations or mixtures thereof.

8. The adsorbent of claim 1 wherein said silicone precursor is selected from polydimethylsiloxanes, polydiphenylsiloxanes, octyl silsesquioxanes methyl silsesquioxanes, (2,4,4-trimethylpentyl) triethoxysilane and mixtures thereof.

9. The adsorbent of claim 1 wherein said silicone precursor is identified by one or more of the following Chemical Abstracts Service (CAS) Registry Numbers: CAS Registry Numbers 63148-62-9, CAS Registry Numbers 63148-59-4, CAS Registry Number of 897393-56-5; CAS Registry Number of 68554-66-5; CAS Registry Number 35435-21-3, and combinations thereof.

10. The adsorbent of claim 1 which comprises from about 2 to about 15% by weight of said silicone derived species.

11. An adsorbent composition for separation of at least 2 gases or liquids wherein there is a size difference between the molecules of said gases or liquids to be separated of 0.8 Å or less, wherein said adsorbent composition is an agglomerated product comprising a surface modified A-type zeolite adsorbent having a starting effective pore size of less than or equal to 4.1 Å wherein the starting pore size of said zeolite is reduced by 0.1 up to about 1.2 Å with a coating comprised of a silicone precursor selected from polydimethylsiloxanes, polydiphenylsiloxanes, octyl silsesquioxanes methyl silsesquioxanes, (2,4,4-trimethylpentyl) triethoxysilane and mixtures thereof, wherein said adsorbent has a particle size of from 0.5-5 mm and a crush strength of at least 0.7 lbF.

12. An adsorption process for adsorbing or separating a first adsorbable component from a gaseous mixture comprising at least a second adsorbable component, wherein the first adsorbable component has a kinetic diameter that is larger than the second adsorbable component and wherein the difference in kinetic diameter between said two adsorbable components is from about 0.1 to about 0.80 Å, said process comprising contacting the mixture with an adsorbent material which selectively adsorbs the second adsorbable component allowing said first adsorbable component to be recovered as product, said process comprising contacting said gaseous mixture with the surface modified zeolite adsorbent composition of claim 1 , such that said zeolite selectively adsorbs said second adsorbable component and not said first adsorbable component.

13. The process of claim 12 wherein said first adsorbable component is CH 4 and said second adsorbable component is N 2 .

14. The process of claim 12 wherein said first adsorbable component is CO and said second adsorbable component is CO 2 .

15. The process of claim 12 wherein said first adsorbable component is N 2 and said second adsorbable component is CO 2 .

16. The process of claim 12 wherein said first adsorbable component is N 2 and said second adsorbable component is O 2 .

Assignees

• Pontonio Steven J
• Stephenson Neil A
• Barrett Philip A
• Stuckert Nicholas R
• Praxair Technology Inc

Inventors

• Pontonio Steven J
• Stephenson Neil A
• Barrett Philip A
• Stuckert Nicholas R

Classifications

• Y02C20/40

  of CO2 · CPC title

• B01J20/2808

  being less than 2 nm, i.e. micropores or nanopores · CPC title

• C10L2290/542

  Adsorption of impurities during preparation or upgrading of a fuel · CPC title

• B01D53/02

  by adsorption, e.g. preparative gas chromatography {(solid sorbent compositions B01J20/00, preparation of inorganic compounds or elements C01)} · CPC title

• B01J20/3078

  Thermal treatment, e.g. calcining or pyrolizing · CPC title