Inorganic matrix composition and composites incorporating the matrix composition

• US 6,969,422 B2
• Filed: 06/01/2001
• Issued: 11/29/2005
• Est. Priority Date: 09/20/2000
• Status: Expired due to Term

• Current Assignee: Goodrich Corporation (Raytheon Technologies Corporation d/b/a RTX)
• Original Assignee: Goodrich Corporation (Raytheon Technologies Corporation d/b/a RTX)
• Inventors: Mazany, Anthony M., Robinson, John W., Cartwright, Craig L.
• Primary Examiner(s): MARCANTONI, PAUL D
• Application Number:
  US09/871,998
• Publication Number:
  US 20020058576A1
• Time in Patent Office: 1,642 Days
• Field of Search: 106/600
• US Class Current: 106/600
• CPC Class Codes: C03C 1/006 to produce glass through wet route
• CPC Class Codes: C03C 25/42 Coatings containing inorganic materials
• CPC Class Codes: C03C 3/064 containing boron
• CPC Class Codes: C03C 3/19 containing boron
• CPC Class Codes: C04B 14/10 Clay sepiolite C04B14/042; grog C04B18/025
• CPC Class Codes: C04B 14/22 Glass ; Devitrified glass
• CPC Class Codes: C04B 14/30 Oxides other than silica ferrites C04B14/363
• CPC Class Codes: C04B 14/386 Carbon carbon nanotubes C04B14/026
• CPC Class Codes: C04B 14/42 Glass
• CPC Class Codes: C04B 14/46 Rock wool ; Ceramic or silicate fibres C04B14/40, C04B14/42 take precedence
• CPC Class Codes: C04B 14/48 Metal
• CPC Class Codes: C04B 16/06 fibrous
• CPC Class Codes: C04B 20/002 Hollow or porous granular materials
• CPC Class Codes: C04B 20/0048 Fibrous materials
• CPC Class Codes: C04B 20/008 Micro- or nanosized fillers, e.g. micronised fillers with particle size smaller than that of the hydraulic binder colloidal silica C04B14/062 ; silica fume C04B18/146
• CPC Class Codes: C04B 2111/00112 Mixtures characterised by specific pH values
• CPC Class Codes: C04B 24/06 containing hydroxy groups
• CPC Class Codes: C04B 24/12 Nitrogen containing compounds organic derivatives of hydrazine hydrazine C04B22/00
• CPC Class Codes: C04B 28/006 containing mineral polymers, e.g. geopolymers of the Davidovits type
• CPC Class Codes: C04B 28/008 Mineral polymers other than those of the Davidovits type, e.g. from a reaction mixture containing waterglass
• CPC Class Codes: C04B 28/26 : Silicates of the alkali metals
• CPC Class Codes: C04B 40/0259 : Hardening promoted by a rise in pressure C04B40/024 takes precedence
• CPC Class Codes: C04B 40/0263 : Hardening promoted by a rise in temperature C04B40/024 takes precedence
• CPC Class Codes: Y02P 40/10 : Production of cement, e.g. improving or optimising the production methods; Cement grinding

Abstract

A modified alkali silicate composition for forming an inorganic network matrix. The modified alkali silicate matrix is made by reacting an alkali silicate (or its precursors such as an alkali hydroxide, a SiO₂ source and water), an acidic inorganic composition, such as a reactive glass, water and optional fillers, additives and processing aids. An inorganic matrix composite can be prepared by applying a slurry of the modified aqueous alkali silicate composition to a reinforcing medium and applying the temperature and pressure necessary to consolidate the desired form. The composite can be shaped by compression molding as well as other known fabrication methods. A notable aspect of the invention is that, although composite and neat resin components prepared from the invention can exhibit excellent dimensional stability to 1000° C. and higher, they can be prepared at the lower temperatures and pressures typical to organic polymer processing.

Claims

1. An inorganic matrix composition comprising the reaction product of an alkali silicate and/or alkali silicate precursors derived from alkali hydroxides or oxides and a silica source, a reactive glass, water, and optionally a clay and/or oxide filler.

2. The composition of claim 1, wherein the alkali silicate is selected from potassium silicate solutions and/or sodium silicate solutions.

3. The composition of claim 1, wherein the alkali silicate is crystalline and/or amorphous sodium silicate and/or potassium silicate.

4. The composition of claim 1 wherein the alkali silicate precursors are alkali hydroxides and/or oxides and a SiO₂ source.

5. The composition of claim 1 wherein the SiO₂ source is an amorphous or crystalline SiO₂ form, selected from the group consisting of silica, silica fume, microsilica, precipitated silica, sand, quartz, quartz flour, silica gels, fumed silica and colloidal silica.

6. The composition of claim 1 wherein the alkali hydroxide is selected from the group consisting of potassium hydroxide and sodium hydroxide.

7. The composition of claim 1 wherein the alkali silicate and/or alkali silicate precursors has a SiO₂/A₂O ratio of about 2.0:

1.0 to 20.0;

1.0, where A is potassium and/or sodium.

8. The composition of claim 1, wherein said reactive glass is acidic and selected from the group of consisting of phosphate glasses, borate glasses and sulfate glasses.

9. The composition of claim 1, wherein the reactive glass is a phosphate glass.

10. The composition of claim 1, wherein the reactive glass is selected from the group consisting of ultraphosphate glasses, borophosphate glasses, silicophosphate glasses, aluminophosphate glasses and mixtures thereof.

11. The composition of claim 1, wherein the reactive glass is an alkali borophosphate glass.

12. The composition of claim 1, wherein the reactive glass is an acidic alkali borophosphate glass.

13. The composition of claim 1, wherein the glass comprises the following formula:

$\underset{k=1}{\overset{n}{\prod <br><br>}}<br><br>\left({\left(M^{p+}\right)}_{q^{\mathrm{\prime <br><br>}}}\right)<br><br>{\left(E^{q-}\right)}_{p^{\mathrm{\prime <br><br>}}}<br><br>{\hspace{1em}<br><br>)}_{r_k}<br><br>\text{\hspace{1em}<br><br>}<br><br>\mathrm{where}<br><br>\text{\hspace{1em}<br><br>}<br><br>\sum <br><br>r_k=1$

where M comprises at least one glass former and at least one metallic glass modifier, E is an oxygen, chalcogenide and/or a halogen atom, p is the cation valence of M, q is the anion valence of E, q′

is number of M cations contained in a network unit, p′

is number of E anions contained in a network unit, r is the molar fraction of that network unit, and n is the number of network units or building blocks and ranges from 2 to about 30.

14. The composition of claim 13 wherein the glass former is selected from the group consisting of boron, silicon, phosphorus, sulfur, germanium, arsenic, antimony, aluminum, and vanadium, and the metallic glass modifier is at least one composition which functions as a flux, selected from the group consisting of lithium, sodium, potassium, rubidium and cesium, and, optionally, a network modifier, selected from the group consisting of vanadium, aluminum, titanium, chromium, manganese, iron, cobalt, nickel, copper, mercury, zinc, thulium, lead, zirconium, lanthanum, cerium, praseodymium, neodymium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, actinium, thorium, uranium, yttrium, gallium, magnesium, calcium, strontium, barium, tin, bismuth, and cadmium.

15. The composition of claim 13 wherein E is selected from the group consisting of oxygen, chalcogenides, halogens, and mixtures thereof.

16. The composition of claim 13 wherein E is selected from the group consisting of oxygen, sulfur, selenium, tellurium, fluorine, and mixtures thereof.

17. The composition of claim 13 wherein M is at least one glass former selected from the group consisting of boron, silicon, phosphorus, sulfur, and at least one metallic glass modifier, selected from the group consisting of vanadium, titanium, zinc, lead, aluminum, zirconium, lanthanum, cerium, neodymium, magnesium, calcium, strontium, barium, lithium, sodium, potassium, rubidium and cesium atoms, and mixtures thereof, and E is an oxygen atom.

18. The composition of claim 1 wherein the reactive glass composition comprises the following formula:

a(A′

₂O)_xb(G_fO)_yc(A″

O)_z

where A′

represents at least one alkali metal glass modifiers, which functions as a fluxing agent, G_f represents at least one glass formers, A″

represents, optionally, at least one glass network modifier, a represents the number of fluxing agents present and ranges from 1 to 5, b represents the number of glass formers present and ranges from 1 to 10, c represents the number of glass network modifiers and ranges from 0 to about 30, x represents the mole fraction of fluxing agent and is between about 0.050 and about 0.150, y represents the mole fraction of glass former and is between about 0.200 and about 0.950, z represents the mole fraction of glass network modifiers and is between about 0.000 and about 0.500, x+y+z=1, and x<

y.

19. The composition of claim 18 wherein A′

is selected from the group consisting of lithium, sodium, potassium, rubidium, and cesium.

20. The composition of claim 18 wherein G_f is selected from the group consisting of boron, silicon, phosphorus, sulfur, germanium, arsenic, antimony, aluminum and vanadium.

21. The composition of claim 18 wherein A″

O is selected from the group consisting of vanadium oxide, titanium oxide, zinc oxide, lead oxide, aluminum oxide, zirconium oxide, lanthanum oxide, cerium oxide, neodymium oxide, magnesium oxide, calcium oxide, strontium oxide, barium oxide, and silicon oxide.

22. The composition of claim 18 wherein A″

O is at least one metallic glass modifier.

23. The composition of claim 18 wherein A″

O is at least two glass modifiers.

24. The composition of claim 18 wherein a is 1, b is 2, and c is 1.

25. The composition of claim 18 wherein a is 1, b is 2 and c is 2, and A′

is Li, G_fO is P₂O₅ and B₂O₃, and A″

O is MgO and BaO.

26. The composition of claim 1 wherein the reactive glass composition comprises the following formula:

(Li₂O)_x(P₂O₅)_y1(B₂O₃)_y2c(A″

O)_z,

wherein A″

O is at least one metallic glass modifiers, c is between 1 and 30, x is between about 0.050 and 0.500, y₁ is between about 0.200 and 0.800, y₂ is between about 0.010 and 0.150, z is between about 0.010 and 0.300, and x+y₁+y₂+z=1.

27. The composition of claim 18 wherein A″

O is selected from the group consisting of magnesium oxide, barium oxide, zinc oxide, silicon oxide, and aluminum oxide.

28. The composition of claim 1, wherein the filler comprises at least one oxide selected from the group consisting of oxides of boron, aluminum, silicon, zinc, gallium, titanium, zirconium, manganese, iron, molybdenum, tungsten, bismuth, lead, lanthanum, cerium, neodymium, yttrium, calcium, magnesium and barium.

29. The composition of claim 1 wherein the clay filler comprises kaolin, calcined kaolin, mica, vermiculite and/or metakaolin.

30. The composition of claim 1, wherein said alkali silicate and/or alkali silicate precursors are present in an amount between about 30 wt. % and 90 wt. % based upon the total composition.

31. The composition of claim 1, wherein said alkali silicate is formed from a alkali hydroxide and a SiO₂ source and said alkali hydroxide is present in an amount of between about 3 wt. % to about 40 wt. % and said SiO₂ source is present in an amount of about 15 wt. % to about 75 wt. % based upon the total composition weight.

32. The composition of claim 1, wherein said reactive glass is present in an amount of between about 0.01 wt. % and about 60 wt. % based upon the total composition.

33. The composition of claim 8, wherein said reactive acidic glass is present in an amount of between about 0.01 wt. % and about 60 wt. % based upon the total composition.

34. The composition of claim 1, wherein said reactive glass is present in an G:

SiO₂ ratio of between about 0.01 and about 50.0.

35. The composition of claim 8, wherein said reactive acidic glass is present in an G:

SiO₂ ratio of between about 0.01 and about 50.0.

36. The composition of claim 1, wherein said clay filler is present in an amount of between about 0.0 wt. % and about 20 wt. % based upon the total composition weight.

37. The composition of claim 1, wherein said oxide filler is present in an amount of between about 0.0 wt. % and about 20 wt. % based upon the total composition weight.

38. The composition of claim 1 comprises the reaction product of the following:

a) 30 to 85 wt. % of at least one alkali silicate;

b) 0.01 to 60 wt. % of at least one reactive glass;

c) 0 to 20 wt. % of at least one clay filler;

d) 0 to 20 wt. % of at least one oxide; and

e) 15 to 60 wt. % of water.

39. The composition of claim 1 comprises the reaction product of the following:

a) 30 to 85 wt. % of at least one silicate or alkali silicate precursor;

b) 0.01 to 60 wt. % of at least one reactive glass;

c) 0 to 20 wt. % of at least one clay filler;

d) 0 to 20 wt. % of at least one oxide; and

e) 15 to 60 wt. % of water.

40. The composition of claim 1 comprises the reaction product of the following:

a) 15 to 75 wt. % of at least one SiO₂ source;

b) 3 to 40 wt. % of at least one alkali hydroxide;

c) 0.01 to 60 wt. % of at least one reactive glass;

d) 0 to 20 wt. % of at least one clay filler;

e) 0 to 20 wt. % of at least one oxide; and

f) 15 to 75 wt. % of water.

44. The composition of claim 1 further includes non-clay filler materials.

45. The composition of claim 44, wherein the non-clay filler materials are selected from the group consisting of fibers, spheres, and particles.

46. The composition of claim 45, wherein the fibers are selected from a group consisting of continuous fibers and discontinuous fibers.

47. The composition of claim 45, wherein the spheres are selected from the group consisting of microspheres, macrospheres, hollow spheres, and solid spheres comprising glass, ceramic, metal, mineral, organic or inorganic materials.

48. The composition of claim 45, wherein the filler materials are utilized for reinforcement and selected from the group consisting of carbon fibers, glass fibers, alkali resistant glass fibers, mineral fibers, organic fibers, ceramic fibers and metallic fibers.

49. The composition of claim 45, wherein the reinforcement materials are selected from the group consisting of graphite fibers, E-glass fibers, S-glass fibers, basalt fibers, stainless steel fibers, titanium fibers, nickel alloy fibers, aramid fibers, polyethylene fibers, silicon carbide fibers and boron nitride fibers.

50. The inorganic matrix composition made from the composition of claim 1 and formed by curing the composition at a temperature ranging from about 15°

C. to 1000°

C. and higher and a pressure range from vacuum at about ambient to 10<sup>−

3</sup> torr, and/or external pressure from ambient to about 20,000 psi.

51. The inorganic matrix composition of claim 50 formed by curing the composition at about 15°

C. to about 200°

C. and an external pressure from ambient to 200 psi and, alternatively, under vacuum at about ambient to 10<sup>−

3</sup> torr.

41. A composition comprising the reaction product of water and the following mixture:

a) 20 to 99.9 wt. % of at least one alkali silicate;

b) 0.01 to 80 wt. % of at least one reactive glass;

c) 0 to 20 wt. % of at least one clay filler; and

d) 0 to 20 wt. % of at least one oxide.

42. A composition comprising the reaction product of water and the following mixture:

a) 20 to 99.9 wt. % of at least one alkali silicate or alkali silicate precursor;

b) 0.01 to 80 wt. % of at least one reactive glass;

c) 0 to 20 wt. % of at least one clay filler; and

d) 0 to 20 wt. % of at least one oxide.

43. A composition comprising the reaction product of water and the following mixture:

a) 20 to 75 wt. % of at least one SiO₂ source;

b) 5 to 40 wt. % of at least one alkali hydroxide;

c) 0.01 to 75 wt. % of at least one reactive glass;

d) 0 to 20 wt. % of at least one clay filler; and

e) 0 to 20 wt. % of at least one oxide.

52. An alkali silicate slurry composition for forming an inorganic polymer network comprising an alkali silicate or a mixture that yields an insitu alkali silicate, a reactive acidic glass, water and operationally a modifier that moderates the gelation of matrix binder suspension and/or a clay and/or oxide filler to enhance physical and thermal properties.

53. The composition of claim 52, wherein the gel modifier is an organic acid or organic base.

54. The composition of claim 52, wherein said organic acid is an α

-hydroxyacid and/or a β

-hydroxyacid.

55. The composition of claim 52, wherein said organic base is substituted nitrogen organic base.

56. The composition of claim 52, wherein said organic base is a substituted pyridine.

57. The composition of claim 52, wherein said organic base is quinoline.

58. The composition of claim 52, wherein said gel modifier is present in an amount of between about 0.0 wt. % and about 10 wt. % based upon the total composition.