Method for preparing a sorbent

Patent metadata

Field	Value
Publication number	US-10343137-B2
Application number	US-201415036817-A
Country	US
Kind code	B2
Filing date	Dec 4, 2014
Priority date	Dec 18, 2013
Publication date	Jul 9, 2019
Grant date	Jul 9, 2019

Abstract

A method for preparing a sorbent precursor, which may be sulphided and used to remove heavy metals such as mercury from fluid streams, includes the steps of:
(i) mixing together an inert particulate support material and one or more binders to form a support mixture, (ii) shaping the support mixture by granulation in a granulator to form agglomerates, (iii) coating the agglomerates with a coating mixture powder including a particulate copper compound and one or more binders to form a coated agglomerate, and (iv) drying the coated agglomerate to form a dried sorbent precursor.

First claim

The invention claimed is:

1. A method for preparing a sorbent precursor comprising the steps of:
(i) mixing together an inert particulate support material and one or more binders to form a support mixture,
(ii) shaping the support mixture by granulation using a liquid in a granulator to form agglomerates,
(iii) coating the agglomerates with a coating mixture powder comprising a particulate copper compound and one or more binders to form a coated agglomerate, and
(iv) drying the coated agglomerate to form a dried sorbent precursor;

wherein the agglomerates are coated in step (iii) by adding the coating mixture powder to the agglomerates in the granulator.

2. The method according to claim 1 wherein the inert particulate support material is an alumina, a metal-aluminate, silicon carbide, silica, titania, zirconia, zinc oxide, an aluminosilicate, a zeolite, a metal carbonate, carbon, or a mixture thereof.

3. The method according to claim 1 wherein the inert particulate support material is an alumina or hydrated alumina.

4. The method according to claim 1 wherein the inert particulate support material is in the form of a powder with a D 50 particle size in the range of from 1-100 μm.

5. The method according to claim 1 wherein the binder used to prepare the agglomerates is a clay binder, cement binder, organic polymer binder, or a mixture thereof.

6. The method according to claim 1 wherein the agglomerates have a diameter in the range of from 1-15 mm.

7. The method according to claim 1 wherein the particulate copper compound is one or more of copper oxide, basic copper carbonate, or a precipitated material comprising copper basic carbonate and zinc basic carbonate.

8. The method according to claim 1 wherein the particulate copper compound is in the form of a powder with an average particle size, [D 50 ], in the range of from 5-100 μm.

9. The method according to claim 1 wherein the copper content of the dried sorbent precursor is in the range of from 0.5-30% by weight (expressed as copper present in the dried material).

10. The method according to claim 1 wherein the copper compound is present as a layer on the surface of the agglomerate and the thickness of the layer in the dried sorbent precursor is in the range of from 1 to 1000 μm (micrometers).

11. The method according to claim 1 wherein the sorbent precursor comprises a mixture of a particulate basic copper carbonate and a clay binder, as a surface layer of 1 to 1000 μm thickness coated on the surface of agglomerates formed from a particulate hydrated alumina support material, which is bound together with a cement binder and a clay binder.

12. The method according to claim 1 wherein the coated agglomerates are dried at a temperature in a range of from 70-150° C.

13. The method for preparing a sorbent comprising preparing a sorbent precursor according to claim 1 and subjecting the dried sorbent precursor to a sulphiding step to convert the copper compound to copper sulphide.

14. The method according to claim 13 wherein the sulphiding step is performed by reacting the copper compound with a sulphur compound that is hydrogen sulphide, an alkali metal sulphide, ammonium sulphide, elemental sulphur or a polysulphide.

15. The method according to claim 13 wherein the sulphiding step is performed using hydrogen sulphide at a concentration in the range of from 0.1 to 5% by volume in an inert gas.

16. The method according to claim 13 wherein the sulphiding step is performed on the dried sorbent precursor composition ex-situ in a sulphiding vessel through which a sulphiding agent is passed, or performed in situ, in which case the dried sorbent precursor composition is installed and undergoes sulphidation in the vessel in which it is used to absorb heavy metals.

Assignees

• Johnson Matthey Plc

Inventors

• Evans Matthew James
• Foran Paul Thomas
• Lunn Matthew David Gwydion

Classifications

• B01D2253/25

  Coated, impregnated or composite adsorbents · CPC title

• B01J20/0237 Primary

  Compounds of Cu · CPC title

• B01D2258/025

  from metallurgy plants · CPC title

• B01J20/2803

  Sorbents comprising a binder, e.g. for forming aggregated, agglomerated or granulated products · CPC title

• B01J20/3007

  Moulding, shaping or extruding · CPC title