IP Library Granted Patent US 10,766,786
Granted Patent B2
US 10,766,786 · App. 15/546,891 · Granted Sep 8, 2020

Mo-doped Co

Inventors: Yajie Chen (Brighton, MA); Vincent Harris (Sharon, MA)
Assignee: ROGERS CORPORATION
C01G51/66C01G39/006C01G49/0036C04B35/2633C04B35/6261C04B35/6262C04B35/62675C04B35/63416C04B35/64H01B1/02H01F1/348H01F27/255H01P1/19H01P1/20H01P1/38C01P2002/77C01P2004/03C01P2006/40C01P2006/42C04B2235/3213C04B2235/3215C04B2235/3256C04B2235/3274C04B2235/3275C04B2235/3277C04B2235/6567C04B2235/6583C04B2235/6585C04B2235/6586C04B2235/662C04B2235/767C04B2235/786C04B2235/788C04B2235/79H01Q1/36
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Quick Facts
Patent No.
US 10,766,786
App. No.
15/546,891
Granted
Sep 8, 2020
Kind
B2
Abstract

A Co 2 Z hexaferrite composition is provided containing molybdenum and one or both of barium and strontium, having the formula (Ba 2 Sr (3-Z) Co (2+X) )Mo x Fe (y-2x) O 41 where x=0.01 to 0.20; y=20 to 24; and z=0 to 3. The composition can exhibit high permeabilities and equal or substantially equal values of permeability and permittivity while retaining low magnetic and dielectric loss tangents and loss factors. The composition is suitable for high frequency applications such as ultrahigh frequency and microwave antennas and other devices.

Claims (89)

1. A hexaferrite composition comprising iron, cobalt, one or both of barium and strontium, and molybdenum, wherein said ferrite composition comprises a Z-type hexaferrite phase, having the formula

(Ba z Sr (3-z) )Co (2+x) Mo x Fe (y-2x) O 41

where x=0.01 to 0.20;

y=20 to 24; and

z=0 to 3.

2. The hexaferrite composition of claim 1 , wherein x=0.08 to 0.15.

3. The hexaferrite composition of claim 1 , wherein x=0.10 to 0.12.

4. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a real permeability at least 3.0 over a frequency range of 0.1 to 3.0 GHz.

5. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a real permeability at least 7.0 over a frequency range of 0.1 to 3.0 GHz.

6. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a real permeability ranging from 7.0 to 12.0 over a frequency range of 0.1 to 3.0 GHz.

7. The hexaferrite composition of claim 1 , wherein z=1.2 to 3.0, and the hexaferrite composition has a real permeability ranging from 8.0 to 12.0 over a frequency range of about 0.1 GHz to at least 1.0 GHz.

8. The hexaferrite composition of claim 1 , wherein z=0 to 0.5, and the hexaferrite composition has a real permeability ranging from 2.0 to 4.0 over a frequency range of about 0.1 GHz to about 3.0 GHz.

9. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a real permittivity at least 6.0 over a frequency range of 0.1 to 3.0 GHz.

10. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a real permittivity at least 8.0 over a frequency range of 0.1 to 3.0 GHz.

11. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a real permittivity ranging from 6.0 to 18.0 over a frequency range of 0.1 to 10.0 GHz.

12. The hexaferrite composition of claim 1 , wherein a real permittivity of the hexaferrite composition is equal to a real permeability of the hexaferrite composition within 10%.

13. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a characteristic impedance matching an impedance of free space within 3%.

14. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a dielectric loss tangent, tan δ ε , less than 0.02 at a frequency of 0.1 to 0.8 GHz.

15. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a dielectric loss tangent, tan δ ε , less than 0.16 at a frequency of 0.1 to 1.0 GHz.

16. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a magnetic loss tangent tan δ μ approximately 0.1 at 0.4 GHz.

17. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a magnetic loss tangent tan δ μ less than 0.3 at a frequency of 0.1 to 0.8 GHz.

18. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a magnetic loss tangent tanδ μ less than 0.95 at a frequency of 0.1 to 3.5 GHz.

19. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a magnetic loss tangent, tan δ μ , ranging from 0.1 to 1.0 over a frequency range of 0.1 to 1.0 GHz.

20. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a dielectric loss factor tan δ ε /ε′ less than 0.001 at a frequency of 0.8 GHz.

21. The hexaferrite composition of claim 1 , wherein the hexaferrite composition has a magnetic loss factor tan δ μ /μ′ less than 0.03 at a frequency of 0.8 GHz.

22. An article comprising the hexaferrite composition of claim 1 .

23. The article of claim 22 , wherein the article is an antenna, filter, inductor, circulator, or phase shifter.

24. The article of claim 22 , wherein the article is a microwave antenna.

25. The article of claim 24 , wherein the article is an antenna operable at a frequency equal to or greater than 0.1 GHz.

26. The article of claim 24 , wherein the article is an antenna operable at a frequency equal to or greater than 0.3 GHz.

27. The article of claim 24 , wherein the article is an antenna operable at 0.1 to 1.5 GHz.

28. The article of claim 24 , wherein the article is an antenna operable at 0.3 to 1.0 GHz.

29. The article of claim 22 , further comprising a second hexaferrite composition comprising a Z-type hexaferrite phase having the formula

(Ba z Sr (3-z) )Co (2+x) Mo x Fe (y-2x) O 41

where x=0.01 to 0.20;

y=20 to 24; and

z=0 to 3; and

wherein the amount of Ba and the amount of Sr in the hexaferrite composition and the second hexaferrite composition differ.

30. The article of claim 29 , wherein a cutoff frequency of the second hexaferrite composition is higher than a cutoff frequency of the hexaferrite composition.

31. The article of claim 29 , wherein the hexaferrite composition has a real permeability ranging from 8.0 to 12.0 over a frequency range of about 0.1 GHz to at least 1.0 GHz, and the second hexaferrite composition has a real permeability ranging from 2.0 to 4.0 over a frequency range of about 0.1 GHz to about 3.0 GHz.

32. The article of claim 22 , wherein the article is a giant magnetoresistant device or a giant tunneling magnetoresistant device.

33. A method of making a hexaferrite composition comprising:

(a) providing hexaferrite phase precursor compounds comprising Fe, Ba, Co, and Mo,

(b) calcining the hexaferrite phase precursor compounds in air to form a material comprising a Z-type hexaferrite phase.

34. The method of claim 33 , wherein the hexaferrite phase precursor compounds comprise oxides of Fe, Ba, Co, and Mo.

35. The method of claim 33 , wherein the hexaferrite phase precursor compounds comprise MoO 2 , BaCO 3 , Co 3 O 4 , and Fe 2 O 3 .

36. The method of claim 33 , wherein the hexaferrite phase precursor compounds comprise 0 to 0.96 wt. % MoO 2 , 22.10 to 22.18 wt. % BaCO 3 , 6.02 to 6.59 wt. % Co 3 O 4 , and 70.35 to 71.8 wt. % Fe 2 O 3 .

37. The method of claim 33 , wherein in step (b), the precursor compounds are calcined at 1000 to 1300° C.

38. The method of claim 33 , further comprising:

(c) crushing the material formed in step (b) to form a powder mixture, and

(d) sintering the powder mixture.

39. The method of claim 38 , wherein the powder mixture is sintered at 1200 to 1280° C. for 4 to 20 hours in an oxygen atmosphere.

40. The method of claim 38 , further comprising forming the powder mixture into a compact prior to step (d).

41. The method of claim 38 , further comprising adding a binder to the powder mixture.

42. The method of claim 41 , wherein the binder is selected from the group consisting of a polyvinyl alcohol, methyl cellulose, polyethylene glycol, and poly(alkylene carbonate).

43. The method of claim 41 , wherein the binder is polyvinyl alcohol comprising 8% to 12% by weight of the powder mixture.

44. The method of claim 38 , further comprising:

(e) crushing the material formed in step (d) to form a powder mixture; and

(f) annealing the powder mixture formed in step (e).

45. The method of claim 44 , wherein the powder mixture is annealed at 800 to 1000° C. for 9 to 20 hours.

46. The hexaferrite composition of claim 1 , wherein

x=0.08 to 0.15; and

the hexaferrite composition has

a real permeability at least 3.0 over a frequency range of 0.1 to 3.0 GHz,

a real permittivity at least 6.0 over a frequency range of 0.1 to 3.0 GHz,

a dielectric loss tangent, tan δ ε , less than 0.16 at a frequency of 0.1 to 0.8 GHz, and

a magnetic loss factor tan δ μ /μ′ less than 0.03 at a frequency of 0.8 GHz.

47. The hexaferrite composition of claim 46 , wherein

z=0 to 0.5, and

the hexaferrite composition has a real permeability ranging from 3.0 to 4.0 over a frequency range of about 0.1 GHz to about 3.0 GHz.

48. The hexaferrite composition of claim 1 , wherein

x=0.10 to 0.12; and

the hexaferrite composition has

a real permeability at least 7.0 over a frequency range of 0.1 to 3.0 GHz,

a real permittivity at least 8.0 over a frequency range of 0.1 to 3.0 GHz,

a dielectric loss tangent, tan δ ε , less than 0.02 at a frequency of 0.1 to 1.0 GHz, and

a dielectric loss factor tan δ ε /ε′ less than 0.001 at a frequency of 0.8 GHz.

49. The hexaferrite composition of claim 48 , wherein

z=1.2 to 3.0, and

the hexaferrite composition has a real permeability ranging from 8.0 to 12.0 over a frequency range of about 0.1 GHz to at least 1.0 GHz.

50. An article comprising the hexaferrite composition of claim 46 , wherein the article is an antenna, filter, inductor, circulator, or phase shifter.

51. An article comprising the hexaferrite composition of claim 48 , wherein the article is an antenna, filter, inductor, circulator, or phase shifter.

52. A method of making a hexaferrite composition comprising:

(a) providing hexaferrite phase precursor compounds comprising more than 0 to 0.96 wt. % MoO 2 , 22.10 to 22.18 wt. % BaCO 3 , 6.02 to 6.59 wt. % Co 3 O 4 , and 70.35 to 71.8 wt. % Fe 2 O 3 ,

(b) calcining the hexaferrite phase precursor compounds at 1000 to 1300° C. in air to form a material comprising a Z-type hexaferrite phase;

(c) crushing the material formed in step (b) to form a powder mixture, forming the powder mixture and a binder into a compact, and

(d) sintering the compact at 1200 to 1280° C. for 4 to 20 hours in an oxygen atmosphere.

(e) crushing the material formed in step (d) to form a second powder mixture; and

(f) annealing the second powder mixture formed in step (e) at 800 to 1000° C. for 9 to 20 hours.

Assignments (3)
SECURITY INTEREST Recorded Oct 16, 2020
From: ROGERS CORPORATION
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 054090/0037 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 17, 2018
From: CHEN, YAJIE; HARRIS, VINCENT
To: NORTHEASTERN UNIVERSITY
Reel/Frame 044636/0138 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 17, 2018
From: NORTHEASTERN UNIVERSITY
To: ROGERS CORPORATION
Reel/Frame 044636/0155 →
Continuity (2)
Provisional Application 62110025 · Jan 30, 2015
Related Publication 20180016157A1 · Jan 18, 2018
Cited By (2)
US 12,381,025 US 12,424,362