IP Library Granted Patent US 7,053,125
Granted Patent B2
US 7,053,125 · App. 10/336,636 · Granted May 30, 2006

Controlled dispersion of colloidal suspension by comb polymers

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Quick Facts
Patent No.
US 7,053,125
App. No.
10/336,636
Granted
May 30, 2006
Kind
B2
Abstract

Comb polymers are used as dispersants to increase the stability of colloidal suspensions containing multivalent or high concentrations of monovalent ions. Stabilized colloidal suspensions and methods of forming stabilized colloidal suspensions are described, including suspensions containing ceramic precursors or bioactive agents useful in forming ceramic substrates or pharmaceutical compositions, respectively.

Claims (77)

1. A colloidal suspension comprising:

particles selected from the group consisting of metals, ceramic precursors, semiconductors, polymers, biodegradable polymers, bioactive agents, and mixtures thereof;

a comb polymer; and

multivalent ions,

wherein said suspension comprises said multivalent ions at a concentration of at least 0.001 M,

the particles have an average effective diameter from 1 nanometer to 3 microns,

the comb polymer comprises a polymer having ionizable and nonionizable side-chains, and

a ratio of the ionizable to the nonionizable side-chains is from 20:1 to 1:1.

2. The colloidal suspension of claim 1 , wherein the particles are stabilized against flocculation.

3. The colloidal suspension of claim 1 , wherein the colloidal suspension comprises water.

4. The colloidal suspension of claim 3 , wherein the colloidal suspension further comprises a liquid less polar than water.

5. The colloidal suspension of claim 4 , wherein said liquid less polar than water is selected from the group consisting of alcohol, methanol, propanol, ethanol, t-butanol, N,N-dimethylformamide, dimethyl sulfoxide, acetone, acetonitrile, acetic acid, hexamethylphosphoric triamide, tetrahydrofuran, N, N-d imethylacetamide, N-methyl-2-pyrrolidone, tetramethyl urea, glycerol, ethylene g lycol, and mixtures thereof.

6. The colloidal suspension of claim 1 , wherein said particles have an average effective diameter from 20 nanometers to 3 microns.

7. The colloidal suspension of claim 1 , wherein said particles are selected from the group consisting of tool steels, molybdenum, nickel, gold, silver, platinum, titanium-aluminum-vanadium alloys, tungsten, aluminum, alloys thereof, and mixtures thereof.

8. The colloidal suspension of claim 1 , wherein said particles are selected from the group consisting of hydroxyapatite, titanium oxide, lead zirconate, titanate, alumina, silica, zirconia, silicon nitride, silicon carbide, and mixtures thereof.

9. The colloidal suspension of claim 1 , wherein said particles are selected from the group consisting of acrylic latexes, poly(ethyl methacrylate), cellulose polystyrene, poly(methyl methacrylate), poly(lactic acids), natural rubber, polyethylene, poly(vinyl chloride), and mixtures thereof.

10. The colloidal suspension of claim 1 , wherein said particles comprise a bioactive agent selected from the group consisting of drugs, proteins, enzymes, polynucleotides, lipoproteins, liposomes, polypeptides, chemotherapeutic agents, hormones, polysaccharides, steroids, analgesics, local anesthetics, antibiotic agents, anti-inflammatory corticosteroids, and mixtures thereof.

11. The colloidal suspension of claim 1 , wherein the ionizable side-chains comprise a carboxylic acid moiety and the nonionizable side-chains comprise a polyethylene oxide moiety.

12. The colloidal suspension of claim 1 , wherein the comb polymer has a backbone having an average molecular weight from 1,000 to 15,000.

13. The colloidal suspension of claim 1 , wherein said multivalent ions are selected from the group consisting of alkaline earth metal ions, Group IIIA metal ions, Group IVA metal ions, Al 3+ , Sn 4+ , Pb 4+ , Ti 3+ , Cr 3+ , Mn 3+ , Fe 3+ , Ni 2+ , Cu 2+ , Co 3+ , Ir 3+ , CO 3 2− , PO 4 3− , SO 3 2− , S 2− , Te 2− , Se 2− , N 3− , P 3− , O 2− , and mixtures thereof.

14. The colloidal suspension of claim 1 , wherein said ion concentration is at least 0.01 M.

15. The colloidal suspension of claim 1 , wherein said ion concentration is at least 0.1 M.

16. A colloidal suspension comprising:

particles selected from the group consisting of metals, ceramic precursors, semiconductors, polymers, biodegradable polymers, bioactive agents, and mixtures thereof;

a comb polymer; and

monovalent ions,

wherein said suspension comprises said monovalent ions at a concentration of at least 0.1 M,

the particles have an average effective diameter of from 1 nanometer to 3 microns,

the comb polymer comprises a polymer having ionizable and non-ionizable side chains, and

a ratio of the ionizable to non-ionizable side chains is from 20:1 to 1:1.

17. The colloidal suspension of claim 16 , wherein the particles are stabilized against flocculation.

18. The colloidal suspension of claim 16 , wherein the colloidal suspension comprises water.

19. The colloidal suspension of claim 18 , wherein the colloidal suspension further comprises a liquid less polar than water.

20. The colloidal suspension of claim 19 , wherein said liquid less polar than water is selected from the group consisting of alcohol, methanol, propanol, ethanol, t-butanol, N,N-dimethylformamide, dimethyl sulfoxide, acetone, acetonitrile, acetic acid, hexamethylphosphoric triamide, tetrahydrofuran, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, tetramethyl urea, glycerol, ethylene glycol, and mixtures thereof.

21. The colloidal suspension of claim 16 , wherein said particles have an average effective diameter from 20 nanometers to 3 microns.

22. The colloidal suspension of claim 16 , wherein said particles are selected from the group consisting of tool steels, molybdenum, nickel, gold, silver, platinum, titanium-aluminum-vanadium alloys, tungsten, aluminum, alloys thereof, and mixtures thereof.

23. The colloidal suspension of claim 16 , wherein said particles are selected from the group consisting of hydroxyapatite, titanium oxide, lead zirconate, titanate, alumina, silica, zirconia, silicon nitride, silicon carbide, and mixtures thereof.

24. The colloidal suspension of claim 16 , wherein said particles are selected from the group consisting of acrylic latexes, poly(ethyl methacrylate), cellulose polystyrene, poly(methyl methacrylate), poly(lactic acids), natural rubber, polyethylene, poly(vinyl chloride), and mixtures thereof.

25. The colloidal suspension of claim 16 , wherein said particles comprise a bioactive agent selected from the group consisting of drugs, proteins, enzymes, polynucleotides, lipoproteins, polypeptides, chemotherapeutic agents, hormones, polysaccharides, steroids, analgesics, local anesthetics, antibiotic agents, anti-inflammatory corticosteroids, and mixtures thereof.

26. The colloidal suspension of claim 16 , wherein the ionizable side-chains comprise a carboxylic acid moiety and the nonionizable side-chains comprise a polyethylene oxide moiety.

27. The colloidal suspension of claim 16 , wherein the comb polymer has a backbone having an average molecular weight from 1,000 to 15,000.

28. The colloidal suspension of claim 16 , wherein said monovalent ions are selected from the group consisting of halides, ionized alkali earth metals, NH 4 + ; NO 3 − , ClO 3 − , IO 3 − , and mixtures thereof.

29. The colloidal suspension of claim 16 , wherein said ion concentration is at least 0.5 M.

30. The colloidal suspension of claim 16 , wherein said ion concentration is at least 1.0 M.

31. A colloidal suspension comprising:

particles selected from the group consisting of hydroxyapatite, titanium oxide, lead zirconate, titanate, alumina, silica, zirconia, silicon nitride, silicon carbide, and mixtures thereof;

a comb polymer; and

multivalent ions,

wherein said suspension comprises said multivalent ions at a concentration of at least 0.001 M,

the particles have an average effective diameter from 1 nanometer to 3 microns,

the comb polymer comprises a polymer having ionizable and nonionizable side-chains, and

a ratio of the ionizable to the nonionizable side-chains is from 20:1 to 1:1.

32. A colloidal suspension comprising:

particles selected from the group consisting of hydroxyapatite, titanium oxide, lead zirconate, titanate, alumina, silica, zirconia, silicon nitride, silicon carbide, and mixtures thereof;

a comb polymer; and

monovalent ions,

wherein said suspension comprises said monovalent ions at a concentration of at least 0.1 M,

the particles have an average effective diameter of from 1 nanometer to 3 microns,

the comb polymer comprises a polymer having ionizable and non-ionizable side chains, and

a ratio of the ionizable to non-ionizable side chains is from 20:1 to 1:1.

33. In a colloidal suspension including ceramic precursor particles, multivalent ions at a concentration of at least 0.001 M, a carrier liquid, and a dispersant, the improvement comprising at least one comb polymer as the dispersant,

wherein the particles have an average effective diameter from 1 nanometer to 3 microns.

the comb polymer comprises a polymer having ionizable and nonionizable side-chains, and

a ratio of the ionizable to the nonionizable side-chains is from 20:1 to 1:1.

34. In a colloidal suspension including ceramic precursor particles having an average effective diameter of from 1 nanometer to 3 microns, monovalent ions at a concentration of at least 0.1 M, a carrier liquid, and a dispersant, the improvement comprising at least one comb polymer as the dispersant, wherein the comb polymer comprises a polymer having ionizable and non-ionizable side chains in a ratio of ionizable to non-ionizable side chains of from 20:1 to 1:1.

35. The colloidal suspension of claim 1 ,

wherein said suspension is a pharmaceutical composition,

said particles comprise a bioactive agent, and

said comb polymer comprises ionizable and nonionizable side-chains.

36. The pharmaceutical composition of claim 35 , wherein said comb polymer is water-soluble.

37. The pharmaceutical composition of claim 35 , wherein said comb polymer is bio-compatible.

38. The colloidal suspension of claim 16 ,

wherein said suspension is a pharmaceutical composition,

said particles comprise a bioactive agent, and

said comb polymer comprises ionizable and nonionizable side-chains.

39. The pharmaceutical composition of claim 38 , wherein said comb polymer is water-soluble.

40. The pharmaceutical composition of claim 38 , wherein said comb polymer is bio-compatible.

Assignments (9)
RELEASE OF SECURITY INTEREST Recorded Sep 27, 2022
From: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
To: DE NEEF CONSTRUCTION CHEMICALS (US) INC.; VERIFI LLC; GCP APPLIED TECHNOLOGIES INC.
Reel/Frame 061553/0521 →
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 →
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 →
SECURITY INTEREST Recorded Mar 7, 2016
From: GCP APPLIED TECHNOLOGIES INC.
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENT
Reel/Frame 038012/0407 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2016
From: W. R. GRACE & CO.-CONN.
To: GCP APPLIED TECHNOLOGIES INC.
Reel/Frame 037701/0396 →
RELEASE OF SECURITY INTEREST Recorded Feb 2, 2016
From: GOLDMAN SACHS BANK USA
To: W. R. GRACE & CO.-CONN.
Reel/Frame 037681/0323 →
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2003
From: CHEUNG, JOSEPHINE HO-WAH; JEKNAVORIAN, ARA AVEDIS
To: W.R. GRACE & CO.-CONN.
Reel/Frame 014260/0321 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2003
From: LEWIS, JENNIFER A.; KIRBY, GLEN
To: BOARD OF TRUSTEES OF UNIVERSITY OF ILLINOIS
Reel/Frame 014260/0340 →