Lubrication of transfer plates using an oil or oil in water emulsions

Patent metadata

Field	Value
Publication number	US-11312919-B2
Application number	US-202017076067-A
Country	US
Kind code	B2
Filing date	Oct 21, 2020
Priority date	Mar 11, 2013
Publication date	Apr 26, 2022
Grant date	Apr 26, 2022

Abstract

This disclosure relates to transfer plate lubricant compositions and methods of transporting open containers across stationary transfer plates.

First claim

We claim:

1. A method of lubricating a stationary transfer plate comprising diluting a concentrated lubricant composition to form a dilute lubricant composition and applying the dilute lubricant composition to a stationary transfer plate, the dilute lubricant composition comprising:
an oil selected from the group of:
a) a water insoluble organic compound including two or more ester linkages;
b) a water insoluble organic compound including three or more oxygen atoms;
c) a water insoluble organic compound including three or more oxygen atoms, one ester group and one or more remaining or free hydroxyl groups;
d) an ester of a long chain carboxylic acid with an alcohol;
e) an ester having an alcohol with 2 or more of the hydroxyl groups each being coupled to a carboxylic acid as an ester group;
f) an ester of a monocarboxylic fatty acid and a di- or poly-carboxylic acid;
g) synthetic ester oil;
h) free fatty acid;
i) synthetic or natural hydrocarbon; and
j) mixtures thereof;

an emulsifier; and
water.

2. The method of claim 1 , wherein the dilute lubricant composition is applied from at least one nozzle or bubbler under the transfer plate at a rate of about 2 to 10 gallons of dilute lubricant composition per hour per nozzle or bubbler.

3. The method of claim 1 , wherein the oil is an ester of a fatty acid selected from the group of octanoic acid, nonanoic acid, decanoic acid, undecanoic acid, dodecanoic acid, palmitic acid, stearic acid, oleic acid, butanoic acid, hexanoic acid, heptanoic acid, adipic acid, succinic acid, glutaric acid, sebacic acid, phthalic acid, trimellitic acid, or mixtures thereof.

4. The method of claim 3 , wherein the fatty acid is esterified with an alcohol selected from the group of a primary aliphatic alcohol, a linear primary alcohol having 3 to 25 carbon atoms, a branched primary alcohol having 3 to 25 carbon atoms, a di- or poly-hydric alcohol, glycerine, erythritol, mannitol, sorbitol, glucose, trimethylolpropane, pentaerythritol, dipentaerythritol, sorbitan, or mixtures thereof.

5. The method of claim 3 , wherein the fatty acid is esterified with an alcohol selected from the group of methanol, ethanol, ethylene glycol, diethylene glycol, neopentyl glycol, tetraethylene glycol, glycerine, erythritol, mannitol, sorbitol, glucose, trimethylolpropane, pentaerythritol, dipentaerythritol, sorbitan, or mixtures thereof.

6. The method of claim 1 , wherein the oil is selected from the group of triglycerides, partial glycerides, phospholipids, cardiolipins, and mixtures thereof.

7. The method of claim 1 , wherein the oil is an ester of a material selected from the group of caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, eleostearic acid, arachic acid, gadoleic acid, behenic acid, erucic acid, or mixtures thereof.

8. The method of claim 1 , wherein the oil is selected from the group of lauric acid glycerides, palmitic acid glycerides, stearic acid glycerides, isostearic acid glycerides, oleic acid glycerides, behenic acid glycerides, erucic acid glycerides, and mixtures thereof.

9. The method of claim 1 , wherein the oil is selected from the group of phosphatidic acids, lecithin, crude lecithin, soybean lecithin, cardiolipins, lysophospholipids, lysolecithins, plasmalogens, phosphosphingolipids, sphingomyelins, phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, N-acylphosphatidylethanolamine, and mixtures thereof.

10. The method of claim 1 , wherein the oil is selected from the group of mineral oil; glycerol; tri(caprate/caprylate) ester of glycerine, caprylate, caprate, or cocoate triglyceride; soyate fatty acid ester of sucrose; diheptanoate ester of poly(ethylene glycol); trimethylol propane trioleate; and mixtures thereof.

11. The method of claim 1 , wherein the emulsifier is a nonionic surfactant.

12. The method of claim 1 , wherein the dilute lubricant composition comprises from about 0.0005 wt. % to about 0.001 wt. % oil.

13. The method of claim 2 , wherein the dilute lubricant composition is applied from up to 6 nozzles or bubblers.

14. The method of claim 2 , wherein the dilute lubricant composition is applied at a rate of about 6 to about 8 gallons per hour per nozzle or bubbler.

15. The method of claim 1 , wherein the dilute lubricant composition is applied continuously.

16. The method of claim 1 , wherein the dilute lubricant composition is applied discontinuously.

17. The method of claim 1 , further comprising transporting containers over the stationary transfer plate in a single file at a rate of up of 2200 containers per minute.

18. The method of claim 1 , further comprising transporting containers across the stationary transfer plate with a forward translational velocity of greater than 40 feet per minute.

19. The method of claim 1 , wherein the oil is applied to the transfer plate in an amount between about 1 and about 100 mg/hour.

20. The method of claim 18 , wherein the containers are filled and open.

Assignees

• Ecolab Usa Inc

Inventors

• Morrison Eric D
• Thompson Chad A

Classifications

• C10M2209/107

  of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106 · CPC title

• C10M2203/1025

  used as base material · CPC title

• C10M2209/108

  etherified · CPC title

• C10M2207/283

  of polyhydroxy compounds · CPC title

• C10M2207/289

  containing free hydroxy groups · CPC title