IP Library Granted Patent US 9,728,220
Granted Patent B2
US 9,728,220 · App. 15/158,422 · Granted Aug 8, 2017

Charge control agent for fluid dynamic bearing motor lubricant

Inventor: Thomas Edward Karis (Aromas, CA)
Assignee: Western Digital Technologies, Inc.
G11B19/2036C10M105/36C10M109/00C10M129/72C10M169/04H01B1/12H02K7/08H02K7/085C10M2207/021C10M2207/025C10M2207/123C10M2207/1233C10M2207/1273C10M2207/282C10M2207/285C10M2207/2825C10N2040/02C10N2230/00C10N2230/10C10N2240/02C10N2240/10C10N2240/204F16C2370/12
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Quick Facts
Patent No.
US 9,728,220
App. No.
15/158,422
Granted
Aug 8, 2017
Kind
B2
Abstract

Embodiments disclosed herein generally relate to magnetic recording systems having a spindle motor and, more particularly, to an optimized lubricant for bearings within the spindle motor. A lubricant used in a fluid dynamic bearing motor has an antioxidant additive and a charge control agent dissolved in a diester base oil. The charge control agent is chemically attached to the same diacid reactant used in the diester lubricant base oil, and is prepared through an esterification reaction. The charge control agent is then dissolved in the lubricant base oil. The charge control agent is soluble in the lubricant, and is resistant to free radical oxidation. The charge control agent effectively controls the charge of the lubricant by creating electron donor/acceptor sites in the lubricant, facilitating an independent electronic pathway through the lubricant.

Claims (23)

1. A solution, comprising:

a lubricant that includes a first acid reactant;

a soluble charge control agent including a second acid reactant; and

an antioxidant additive, wherein the first acid reactant and the second acid reactant are the same.

2. The solution of claim 1 , wherein the first and second acid reactants are sebacic acid.

3. The solution of claim 2 , wherein the soluble charge control agent is chemically attached to the lubricant through an esterification reaction.

4. The solution of claim 3 , wherein the soluble charge control agent is dibenzyl sebacate.

5. The solution of claim 4 , wherein one reactant used in the esterification reaction is benzyl alcohol.

6. The solution of claim 3 , wherein the soluble charge control agent is dinaphthyl sebacate.

7. The solution of claim 6 , wherein one reactant used in the esterification reaction is naphthyl alcohol.

8. The solution of claim 3 , wherein one reactant used in the esterification reaction is anthracene methanol.

9. The solution of claim 3 , wherein one reactant used in the esterification reaction is pyrene methanol.

10. The solution of claim 1 , wherein the soluble charge control agent is an asymmetric aryl ester.

11. The solution of claim 1 , wherein the first and second acid reactants are a poly-acid.

12. The solution of claim 1 , wherein the first and second acid reactants are a mono-acid.

13. The solution of claim 1 , wherein the relative permittivity of the lubricant and soluble charge control agent solution is between about 2.5 and 200.

14. The solution of claim 1 , wherein the relative permittivity of the lubricant and soluble charge control agent solution is less than 100.

15. The solution of claim 1 , wherein the conductivity of the lubricant and soluble charge control agent solution is between about 1 and 100 nS/m.

16. The solution of claim 1 , wherein the conductivity of the lubricant and soluble charge control agent solution is greater than 4 nS/m.

17. The solution of claim 1 , wherein the soluble charge control agent is an aryl ester, the concentration of the aryl ester charge control agent being 0.1 to 10% by weight.

18. The solution of claim 17 , wherein the concentration of the aryl ester charge control agent is between 1 and 5% by weight.

19. The solution of claim 1 , wherein the soluble charge control agent is an asymmetric aryl ester or an asymmetric alkyl ester that is liquid at room temperature.

20. The solution of claim 19 , wherein the asymmetric aryl ester or asymmetric alkyl ester is used as a base oil of the lubricant with a concentration of 90 to 100% by weight.

Assignments (7)
PATENT COLLATERAL AGREEMENT - A&R LOAN AGREEMENT Recorded Aug 21, 2023
From: WESTERN DIGITAL TECHNOLOGIES, INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 064715/0001 →
PATENT COLLATERAL AGREEMENT - DDTL LOAN AGREEMENT Recorded Aug 21, 2023
From: WESTERN DIGITAL TECHNOLOGIES, INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 067045/0156 →
RELEASE OF SECURITY INTEREST AT REEL 052915 FRAME 0566 Recorded Feb 8, 2022
From: JPMORGAN CHASE BANK, N.A.
To: WESTERN DIGITAL TECHNOLOGIES, INC.
Reel/Frame 059127/0001 →
SECURITY INTEREST Recorded Feb 6, 2020
From: WESTERN DIGITAL TECHNOLOGIES, INC.
To: JPMORGAN CHASE BANK, N.A., AS AGENT
Reel/Frame 052915/0566 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT SERIAL NO 15/025,946 PREVIOUSLY RECORDED AT REEL: 040831 FRAME: 0265. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Sep 15, 2017
From: HGST NETHERLANDS B.V.
To: WESTERN DIGITAL TECHNOLOGIES, INC.
Reel/Frame 043973/0762 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2016
From: HGST NETHERLANDS B.V.
To: WESTERN DIGITAL TECHNOLOGIES, INC.
Reel/Frame 040831/0265 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 19, 2016
From: KARIS, THOMAS EDWARD
To: HGST NETHERLANDS B.V.
Reel/Frame 038644/0729 →
Continuity (2)
Continuation 14495124 · Sep 24, 2014
Related Publication 20160260453A1 · Sep 8, 2016