IP Library › Granted Patent US 9,546,339
Granted Patent B2
US 9,546,339 · App. 14/279,904 · Granted Jan 17, 2017

Method for reducing crystallization of 1-[di(4-octylphenyl)aminomethyl]tolutriazole

Inventors: Steven G. Donnelly (Bethel, CT); Kevin J. Chase (Branford, CT); William T. Wallack (Stamford, CT)
Assignee: VANDERBILT CHEMICALS, LLC
C10M141/06C10M133/02C10M133/12C10M133/44C10M2215/064C10M2215/223C10N2230/70
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Quick Facts
Patent No.
US 9,546,339
App. No.
14/279,904
Granted
Jan 17, 2017
Kind
B2
Abstract

1-[di(4-octylphenyl)aminomethyl]tolutriazole is prepared in a mineral oil and blended with a liquid alkylated diphenylamine. The liquid product shows increased storage stability with respect to crystallization of the 1-[di(4-octylphenyl)aminomethyl]tolutriazole when the amine is added. This blend product can be stored for a prolonged period of time, and then utilized in a lubricant composition as an antioxidant and corrosion inhibitor.

Claims (15)

1. A method for reducing crystallization of 1-[di(4-octylphenyl)aminomethyl]tolutriazole, comprising the steps of:

(a) blending a component comprising 1-[di(4-octylphenyl)aminomethyl]tolutriazole in process oil with a liquid alkylated diphenylamine so as to obtain a blend composition having about 0.1 to about 50 wt. % amine as part of the total blend composition, and

(b) storing the blend composition obtained in step (a) at room temperature,

wherein the blend composition obtained in step (a) consists of 1-[di(4-octylphenyl)aminomethyl]tolutriazole, the alkylated diphenylamine and process oil.

2. The method of claim 1 , wherein the amine is added to give about 10-40 wt. % amine as part of the total blend composition.

3. The method of claim 1 , wherein the 1-[di(4-octylphenyl)aminomethyl]tolutriazole is diluted at between 40-60% by weight in the process oil.

4. The method of claim 3 , wherein the dilution is about 50% by weight.

5. The method of claim 1 , wherein the alkylated diphenylamine is of the general formula R 5 —C 6 H 4 —NH—C 6 H 4 -R 6 , where R 5 is an alkyl group having 8 to 12 carbon atoms, and R 6 is a hydrogen atom or an alkyl group having 8 to 12 carbon atoms.

6. The method of claim 5 , wherein R 5 is a branched alkyl group having 8 or 9 carbon atoms, and R 6 is a branched alkyl group having 8 or 9 carbon atoms.

7. The method of claim 6 , wherein R 5 and R 6 are the same.

8. The method of claim 1 , wherein the alkylated diphenylamine is chosen from the group consisting of 4,4′-dinonyldiphenylamine in which the nonyl groups are branched; branched octylated/butylated diphenylamine; styrenated and branched octylated/butylated diphenylamine; and mixtures thereof.

9. The method of claim 1 , wherein the alkylated diphenylamine is branched octylated/butylated diphenylamine.

10. The method of claim 9 , wherein the amine is added to give about 10-40 wt. % amine as part of the total blend composition.

11. The method of claim 1 , further comprising the step of, after the storing step, adding the blend composition to a lubricating composition at about 0.1-0.5% by weight of the total lubricating composition based on the weight of the tolutriazole.

12. The method of claim 1 , wherein the amine is branched octylated/butylated diphenylamine and is present in the blend composition at about 10-40 wt. % amine as part of the total blend composition.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 8, 2016
From: DONNELLY, STEVEN G.; CHASE, KEVIN J.; WALLACK, WILLIAM T.
To: VANDERBILT CHEMICALS, LLC
Reel/Frame 040256/0151 →
Continuity (2)
Provisional Application 61824229 · May 16, 2013
Related Publication 20140342957A1 · Nov 20, 2014