IP Library Granted Patent US 6,867,165
Granted Patent B2
US 6,867,165 · App. 10/237,772 · Granted Mar 15, 2005

Calcium hydroxide absorbent with rheology modifier and process involving same

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 6,867,165
App. No.
10/237,772
Granted
Mar 15, 2005
Kind
B2
Abstract

Exemplary carbon dioxide absorbent compositions of the invention incorporate calcium hydroxide, water, and a phosphonic acid or salt thereof. The composition is made into a paste and formed into particles that are conveniently and efficiently processable. When hardened, the particles have excellent carbon dioxide absorbent performance, crush resistance, and pore structure.

Claims (34)

1. A carbon dioxide absorbent, comprising: calcium hydroxide in an amount no less than 83% dry wt and in an amount no greater than 99% dry wt; water in an amount no less than 5% total wt and in an amount no greater than 25% total wt; and a rheology modifier in an amount no less than 0.05% dry wt and in an amount no greater than 5.0% dry wt.

2. The carbon dioxide absorbent of claim 1 wherein said absorbent is in the form of particles having an average length no less than 1 mm and an average length no greater than 10 mm, and having an average width no less than 0.5 mm and an average width no greater than 5.0 mm.

3. The carbon dioxide absorbent of claim 1 further comprising calcium chloride in an amount no less than 0.1% dry wt and in an amount no greater than 6.0% dry wt, and a color indicator dye selected from the group consisting of diethyl violet and thiozol yellow G, said color indicator dye being present in an amount no less than 0.01% dry wt and in an amount no greater than 0.5% dry wt.

4. The carbon dioxide absorbent of claim 3 wherein said wherein said calcium chloride is present in an amount no less than 0.25% dry wt.

5. The carbon dioxide absorbent of claim 4 wherein said color indicator dye is diethyl violet which is present in the amount of 0.02%-0.2% dry wt.

6. The carbon dioxide absorbent of claim 4 further comprising sodium hydroxide, potassium hydroxide, or mixture thereof, being present in an amount no less than 0.01% dry wt and in an amount no greater than 6.0% dry wt.

7. The carbon dioxide absorbent of claim 1 wherein said rheology modifying agent is a phosphonic acid or salt thereof, said rheology modifying agent being present in an amount no less than 0.05% dry wt and in an amount no greater than 5.0% dry wt.

8. The carbon dioxide composition of claim 7 wherein said phosphonic acid or salt is selected from the group consisting of

amino tri (methylene-phosphonic acid) (which is synonymous with phosphonic acid, nitrilotis (methylene)tri);

amino tri (methylene-phosphonic acid), pentasodium salt (which is synonymous with phosphonic acid, nitrilotris (methylene)tri-penta sodium salt);

1-hydroxyethylene-1,1,-diphosphonic acid (which is synonymous with (hydroxyethylidene)diphosphonic acid));

1-hydroxyethylene-1,1,-diphosphonic acid tetra sodium salt (which is synonymous with hydroxyethylidene diphosphonic acid tetra sodium salt);

diethylenetriamine penta(methylene phosphonic acid) (which is synonymous with phosphonic acid), [(phosphonomethyl)imino]bis[2,1-ethanediylnitrilobis(methylene)]] tetrakis;

diethylenetriamine penta(methylene phosphonic acid), pentasodium salt (which is synonymous with phosphonic acid, [(phosphonomethyl)imino]bis[2,1-ethanediylnitrilobis(methylene)]]tetrakis, pentasodium salt; and

2-phosphonobutane-1,2,4-tricarboxylic acid.

9. The carbon dioxide composition of claim 7 wherein said phosphonic acid or salt is selected from the group consisting of

phosphonic acid, nitrilotis (methylene)tri;

phosphonic acid, nitrilotris (methylene)tri-penta sodium salt;

hydroxyethylidene diphosphonic acid;

hydroxyethylidene diphosphonic acid tetra sodium salt;

phosphonic acid, [(phosphonomethyl)imino]bis[2,1-ethanediylnitrilobis(methylene)]]tetrakis;

phosphonic acid, [(phosphonomethyl)imino]bis[2,1-ethanediylnitrilobis(methylene)]]tetrakis, pentasodium salt; and

2-phosphonobutane-1,2,4-tricarboxylic acid.

10. The carbon dioxide composition of claim 7 wherein said phosphonic acid or salt is diethylenetriamine penta(methylene phosphonic acid) or the salt thereof.

11. The carbon dioxide composition of claim 7 wherein said rheology modifier is diethylenetriamine penta(methylenephosphonic acid).

12. The carbon dioxide absorbent of claim 7 wherein said rheology modifier is present in an amount no less than 0.1% dry wt and in an amount no greater than 1.5% dry wt.

13. The carbon dioxide absorbent of claim 12 wherein said rheology modifier is present in an amount no greater than 0.6% dry wt.

14. The carbon dioxide absorbent of claim 7 wherein water is present in an amount no less than 12% total wt and in an amount no greater than 19% total wt.

15. The carbon dioxide absorbent of claim 1 wherein the particles have a porosity of 20-60% dry wt.

16. A carbon dioxide absorbent, comprising: calcium hydroxide, water, sodium and/or potassium hydroxide, calcium chloride, a pH-sensitive color indicator dye, and a phosphonic acid or salt thereof.

17. The carbon dioxide absorbent of claim 16 wherein said color indicator dye is selected from the group consisting of diethyl violet and thiazol yellow G.

18. The carbon dioxide absorbent of claim 17 wherein the particles have a porosity of 30-45% dry wt.

19. A process for making a carbon dioxide absorbent, comprising: combining calcium hydroxide, water, and a phosphonic acid or salt therof to form a paste; forming said paste into particles; and allowing or causing said particles to harden.

20. The process of claim 19 wherein, in said forming step, said paste is extruded, molded, or pelletized.

Assignments (8)
SECURITY INTEREST Recorded Aug 16, 2021
From: MOLECULAR PRODUCTS US HOLDINGS, INC.
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 057195/0531 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2019
From: HENKEL IP & HOLDING GMBH
To: MOLECULAR PRODUCTS US HOLDINGS, INC.
Reel/Frame 049612/0179 →
RELEASE OF SECURITY AGREEMENT RECORDED AT REEL/FRAME NO.: 032159/0384 Recorded Apr 3, 2018
From: GOLDMAN SACHS BANK USA, AS THE COLLATERAL AGENT
To: W.R. GRACE & CO.-CONN.
Reel/Frame 045832/0887 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2017
From: GCP APPLIED TECHNOLOGIES INC.
To: HENKEL IP & HOLDING GMBH
Reel/Frame 043107/0890 →
RELEASE OF SECURITY INTEREST Recorded Jul 14, 2017
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: W. R. GRACE & CO.-CONN.
Reel/Frame 043007/0047 →
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICATION NUMBER 13353676 PREVIOUSLY RECORDED ON REEL 037701 FRAME 0396. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 17, 2016
From: W. R. GRACE & CO.-CONN.
To: GCP APPLIED TECHNOLOGIES INC.
Reel/Frame 038289/0821 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2016
From: W. R. GRACE & CO.-CONN.
To: GCP APPLIED TECHNOLOGIES INC.
Reel/Frame 037701/0396 →
SECURITY AGREEMENT Recorded Feb 4, 2014
From: W.R. GRACE & CO.-CONN.
To: GOLDMAN SACHS BANK USA, AS THE COLLATERAL AGENT
Reel/Frame 032159/0384 →