Lubricating solutions are used on conveying systems in the beverage industry during the filling of containers with beverages. Lubricating compositions of the present invention, especially those designed for use in beverage conveying systems for contained beverages, comprise at least the following components:

a) an alkyl alkoxylated (e.g., ethoxylated or propoxylated, preferably ethoxylated) phosphate ester,

b) aryl (e.g., aromatic, such as phenol) alkoxylated (e.g., ethoxylated or propoxylated) phosphate ester,

c) an aromatic or linear quaternary ammonium antimicrobial agent, and

d) a liquid carrier, such as water.

These lubricating solutions are capable of providing good lubricity and antimicrobial activity over a prolonged time.

Patent
   5863871
Priority
Jan 05 1998
Filed
Jan 05 1998
Issued
Jan 26 1999
Expiry
Jan 05 2018
Assg.orig
Entity
unknown
0
35
EXPIRED
1. An antimicrobial conveyor lubricant comprising:
a) an alkyl phosphate ester,
b) an aryl phosphate ester,
c) a quaternary ammonium antimicrobial agent, and
d) water.
11. A process for lubricating a conveyor used to transport containers, said process comprising applying a composition to the conveying surface of a conveyor, said composition comprising:
a) an alkyl alkoxylated phosphate ester,
b) an aryl alkoxylated phosphate ester,
c) a quaternary ammonium antimicrobial agent, and
d) water,
and then moving containers on said conveyor.
2. The lubricant of claim 1 wherein said alkyl phosphate ester and said aryl phosphate ester are present in a weight to weight ratio of 1.5:1 to 10.0:1 with respect to the quaternary ammonium antimicrobial agent.
3. The lubricant of claim 1 wherein the total weight of said alkyl phosphate ester and said aryl phosphate ester are present in a weight to weight ratio of 2.0:1 to 10.0:1 with respect to quaternary ammonium antimicrobial agent, which is a linear quaternary ammonium antimicrobial agent.
4. The lubricant of claim 1 wherein sodium hydroxide is present in said lubricant.
5. The lubricant of claim 1 wherein a chelating agent for divalent cations is present in said lubricant.
6. The lubricant of claim 5 wherein said chelating agent comprises an amine-substituted acetic acid.
7. The lubricant of claim 1 wherein said aryl phosphate ester comprises a phenol ester wherein said phenol group is not substituted with alkyl groups.
8. The lubricant of claim 1 wherein the pH of the lubricant is less than 8.5.
9. The lubricant of claim 1 wherein the pH of the lubricant is between 4.5 and 8∅
10. The lubricant of claim 1 comprising water, C10-12 alkyl phosphate ester, 5 ethylene oxide units, ethylenediamine tetraacetic acid alkalating agent, didecyl dimethyl ammonium chloride, C12-15 linear alcohol, and phenol ethoxylated phosphate ester.
12. The process of claim 11 wherein said alkyl phosphate ester and said aryl phosphate ester are present in a weight to weight ratio of 1.5:1 to 10.0:1 with respect to the quaternary ammonium antimicrobial agent.
13. The process of claim 11 wherein the total weight of said alkyl phosphate ester and said aryl phosphate ester are present in a weight to weight ratio of 2.0:1 to 10.0:1 with respect to quaternary ammonium antimicrobial agent, which is a linear quaternary ammonium antimicrobial agent.
14. The process of claim 11 wherein sodium hydroxide is present in said lubricant.
15. The process of claim 11 wherein a chelating agent for divalent cations is present in said lubricant.
16. The process of claim 15 wherein said chelating agent comprises an amine-substituted acetic acid.
17. The process of claim 11 wherein said aryl phosphate ester comprises a phenol ester wherein said phenol group is not substituted with alkyl groups.
18. The process of claim 11 wherein the pH of the lubricant is less than 8.5.
19. The process of claim 11 wherein the pH of the lubricant is between 4.5 and 8∅
20. The process of claim 11 wherein said composition comprises water, C10-12 alkyl phosphate ester, ethylene diamine tetraacetic acid or its salts, alkalating agent, didecyl dimethyl ammonium chloride, C12-15 linear alcohol, and phenol ethoxylated phosphate ester.

1. Field of the Invention

The present invention relates to lubricants, especially antimicrobial lubricants, and most especially to antimicrobial lubricants for use in conveyor systems for beverage containers. The lubricants are compatible with beverages and may display reduced deposition of solid materials after the lubricants have contacted spilled beverage.

2. Background of the Art

In the commercial distribution of most beverages, the beverages are packaged in containers of varying sizes, such containers being in the form of cartons, cans, bottles, tetrapack packages, waxed carton packs, and other forms of containers. In most packaging operations, the containers are moved along conveying systems, usually in an upright position (with the opening of the container facing vertically up or down), and moved from station to station, where various operations are performed (e.g., filling, capping, labeling, sealing, etc.). The containers, in addition to their many possible formats and constructions, may comprise many different types of materials, such as metals, glasses, ceramics, papers, treated papers, waxed papers, composites, layered structures, and polymeric materials (e.g., especially polyolefins such as polyethylene, polypropylene, polystyrene and blends thereof, polyesters such as polyethyleneterephthalate and polyethylenenaphthalate and blends thereof, polyamides, polycarbonates, etc.).

There are a number of different requirements which are essential or desirable for antimicrobial lubricants in the conveying systems used to carry containers for beverages. The essential requirements are that the materials provide an acceptable level of lubricity for the system and that the lubricant displays an acceptable antimicrobial activity. It is also desirable that the lubricant have a viscosity which allows it to be applied by conventional pumping and/or application apparatus (e.g., spraying, roller coating, wet bed coating, etc.) as commonly used in the beverage conveyor lubricating art, and that the lubricant is beverage compatible so that it does not form solid deposits when it accidentally contacts spilled beverage on the conveyor system. This last requirement can be especially important since the formation of deposits on the conveyor will change the lubricity of the system and could require shut-down of the equipment to facilitate cleaning. Deposits may occur from the combination of beverage and lubricant in a number of different chemical methods, depending upon the particular beverage and lubricant used. One of the more common forms of deposit is caused by the formation of micelles from the interaction of species, especially different ionic species within the two materials.

Different types of lubricants have been used in the beverage conveying industry with varying degrees of success. A more common type of lubricant is the fatty acid lubricant (either the acid itself or amine salt and/or ester derivatives thereof), some of which are described in U.S. Pat. No. 5,391,308. Another type of lubricant used within this field is the organic phosphate ester, as shown in U.S. Patent No. 4,521,321 and PCT Application WO 96/02616, based upon British patent application Ser. No. 94/14442.5 filed 18 Jul. 1994 (PCT/GB95/01641).

U.S. Pat. No. 5,391,308 discloses phosphate esters other than alkyl or linear esters (e.g., the alkyl aryl phosphate esters described on column 6, lines 11-20 used in combination with the alkyl or linear phosphate esters). The lubricant system of this patent also requires the use of an aqueous based long chain fatty acid composition at a pH of from 9.0 to 10.5 as the lubricant, with specifically combined ingredients to avoid stress cracking in polyethylene terephthalate (PET) bottles transported on a conveyor system. The aromatic-polyoxyalkyl esters are specifically disclosed as part of a combination of esters (along with the alkyl esters) which

". . . results in substantial reduction in stress cracking, thus functioning as the stress cracking inhibiting agent, as well as the emulsifying agent, in the aqueous lubricant concentrate. (Column 3, lines 48-52)."

The reference is specific to fatty acid lubricants, and the specification points out that the use of potassium hydroxide as the saponifying agent, in fatty acid lubricants, has been found to contribute to and to promote stress cracking in P.E.T. (polyethylene terephthalate) bottles. A blend of alkyl phosphate esters and aromatic phosphate esters are shown in combination with the fatty acid lubricant to reduce stress cracking.

PCT Application WO 96/02616 describes the use of lubricant concentrates comprising organic alkyl phosphate esters, aromatic biocidal quaternary ammonium compounds, and sufficient base to provide the concentrate with a pH of from about 5 to about 10.

U.S. Pat. No. 4,521,321 describes lubricants for conveyor systems which comprise dilute aqueous systems of partially neutralized monophosphate aliphatic (e.g., saturated or partially unsaturated linear alkyl). The use of a synergist such as long chain fatty alcohol, fatty acid derived amine oxide, or urea improves the properties of the lubricant.

U.S. Pat. No. 5,062,979 describes lubricants for conveyor systems comprising aqueous, clear-solution-forming, substantially soap-free compositions. These lubricants comprise pH 6-8 compositions comprising alkyl benzene sulfonates, partial phosphate esters with alkoxylated aliphatic alcohols, and aliphatic carboxylic acids. Typical additives such as solubilizers, solvents, foam inhibitors and disinfectants may also be present. The aliphatic carboxylic acids are C6 -C12 fatty acids.

Lubricating compositions of the invention, especially those designed for use in beverage conveying systems for contained beverages, comprise at least the following components:

a) an alkyl alkoxylated (e.g., ethoxylated or propoxylated, preferably ethoxylated) phosphate ester,

b) aryl (e.g., aromatic, such as phenol) alkoxylated (e.g., ethoxylated or propoxylated) phosphate ester,

c) an aromatic or linear quaternary ammonium antimicrobial agent, and

d) a liquid carrier, such as water.

Particularly desirable optional agents with high degrees of utility include chelating agents (e.g., the aminoacetic acid chelating agents such as ethylene diamine tetraacetic acid, EDTA), detergents (e.g., nonionic surfactants) and pH control agents, e.g, potassium or sodium hydroxide.

FIG. 1 shows a graph of data relating the Coefficient of Friction (kinetic) for phosphate esters alone, versus phosphate esters mixed with quaternary ammonium biocides.

FIG. 2 shows a graph of data relating the Coefficient of Friction (kinetic) of phosphate esters lubricating compositions containing either linear quaternary ammonium biocides or aromatic quaternary ammonium biocides.

FIG. 3 shows a graph of data relating the Coefficient of Friction (kinetic) for a lubricant composition of the invention as compared to various lubricant compositions with various couplers (e.g., hydrotropes).

FIG. 4 shows a triangular graph of the effects of variations among anionic surfactants, cationic surfactants and beverage in the practice of the present invention.

Lubricant compositions according the present invention comprise at least the following components:

a) an alkyl alkoxylated (e.g., ethoxylated or propoxylated, preferably ethoxylated) phosphate ester,

b) phenol alkoxylated (e.g., ethoxylated or propoxylated) phosphate ester,

c) an aromatic or linear quaternary ammonium antimicrobial agent, and

d) a liquid carrier, such as water.

The lubricating compositions are usually provided as concentrates which are diluted with the appropriate liquid (e.g., usually water) to up to a 400 times dilution to provide a use solution of the lubricant composition. These compositions are capable of providing a number of beneficial properties as lubricant use solutions, and especially as lubricant use solutions for conveying systems for beverage containers. Each of the ingredients and the various types of properties sought for the lubricant compositions are described below. "Lubricant compositions" is a term used to cover both the lubricant concentrate and the lubricant use solution which is formed by dilution of the concentrate with the appropriate thinning liquid, usually water.

An alkyl alkoxylated (e.g., ethoxylated or propoxylated, preferably ethoxylated) phosphate ester has the general structural formula of:

R1 --O--([CH2 ]m--O)n--PO3 X2

wherein R1 comprises an alkyl group (e.g., linear, branched or cyclic alkyl group of from 1 to 20 carbon atoms, preferably of from 8 to 12 carbon atoms),

m is 2 or 3,

n is 3 to 8 when m is 3, and 3 to 10 when m is 2, and

X is hydrogen, an alkanolamine and/or an alkali metal.

The alkyl groups of R1 may be variously substituted so as to provide a variety of subtle changes in its physical properties, especially with respect to its solubility (e.g., the addition of solubilizing groups or pH adjusting groups) and ionic qualities. Where the phosphate ester comprises an ethoxylated phosphate ester structure, another representative formula would be:

R1 --O--([CH2 ]2 --O)n--PO3 X2

wherein R1 comprises an alkyl group (e.g., linear, branched or cyclic alkyl group of from 1 to 20 carbon atoms, preferably of from 8 to 12 or 10 to 12 carbon atoms),

n is 3 to 8 or 3 to 10, preferably from 4 to 6 with a weight average of about 5, and

X is hydrogen, an alkanolamine and/or an alkali metal.

An aromatic (e.g., aryl, phenol, naphthol, etc.) alkoxylated (e.g., ethoxylated or propoxylated) phosphate ester has the general formula of:

R2 R3 C6 H3 --O--{R4 O}n--PO3 X2

wherein R2 and R3 may be independently selected from the group consisting of hydrogen and alkyl group (e.g., linear, branched or cyclic alkyl group of from 1 to 20 carbon atoms, preferably of from 8 to 12 carbon atoms),

R4 is selected from --CH2 CH2 -- and --CH2 CH2 CH2 --(ethylene and propylene), and

n and X are as defined above.

Again, alkyl groups of R2 and R3 may be variously substituted so as to provide a variety of subtle changes in its physical properties, especially with respect to its solubility (e.g., the addition of solubilizing groups or pH adjusting groups) and ionic qualities. At the present time, it is preferred that R2 and R3 are hydrogen.

The aromatic and/or linear quaternary ammonium antimicrobial agents are materials generally known in the antimicrobial art. This class of compounds may be generally represented by the formula:

R5 R6 R7 R8 N+ X-

wherein R5, R6, R7 and R8 are selected from the group consisting of aryl (e.g., phenyl, furyl, etc.), alkyl arene (e.g., benzyl), hydrogen and alkyl group, with the proviso that no more than two may be hydrogen, and no more than two may be aryl and/or alkyl arene. When any one or more of R5, R6, R7 and R8 are aryl or alkyl arene, the compound is referred to in the art as an aromatic quaternary ammonium compound. It is preferred that no more than two of R5, R6, R7 and R8 have more than 4 carbon atoms, with 8 to 18 carbon atoms being preferred for longer chain alkyl groups. It is possible to have all four of R5, R6, R7 and R8 have from 1 to 4 carbons atoms, with 8-18 carbon atoms preferred, and with independent variations in the number of carbon atoms in the groups and distribution of these groups within the compounds being acceptable.

It is preferred that the composition contain a basic compound, e.g., an alkali metal hydroxide or ammonium salt to control the pH. It is preferred that the composition has a pH of less than 8.5, more preferred that it have a pH less than 8.0 and more preferably that it have a pH between 4.5 and 8.0 or 6.0 and 8∅ The control of the pH level within the range of about 6.0 to about 8.5 has been found to provide another unique benefit to the compositions of the present invention. The antimicrobial activity of the compositions tends to increase significantly when the compositions of pH 6.0 to 8.5 have their pH levels reduced, as by contact with acidic beverages (which most commercial beverages and juices are). This increased activity upon exposure to beverages with a pH lower than that of the lubricant preserves the antimicrobial activity until such time as the activity is needed most, when sustenance is provided for the growth of the microbes, e.g., by the spillage of beverages. As the presence of the beverage tends to reduce the pH of the lubricant, the activity of the antimicrobial agent is better preserved and more efficiently used by such activation.

Although the lubricant compositions of the present invention are novel with any combination of

a) an alkyl alkoxylated (e.g., ethoxylated or propoxylated, preferably ethoxylated) phosphate ester,

b) aromatic (e.g., phenol) alkoxylated (e.g., ethoxylated or propoxylated) phosphate ester,

c) an aromatic or linear quaternary ammonium antimicrobial agent,

(with or without a liquid carrier) there are ranges and proportions of these combinations which provide improved or enhanced performance as compared to the broad range of compositions. For example, the relative proportion of anionic to cationic materials in the lubricant composition (i.e., the relative proportions of the combined total of phosphate ester [anionics] compared to the total of quaternary ammonium microbial agents on a weight to weight basis) affects the degree to which sedimentation, precipitation, cloudiness and deposits occur in the lubricant compositions when contacted with beverages. The higher the proportion of anionics to cationics, the more strongly the compositions resist deposits. It is preferred that the proportion of anionics to cationics is at least 1.5, usually within the range of 2.0 to 10.0, more preferably within the range of 2.0 to 8∅ As noted, the greater the amount of beverage to which the lubricant is likely to be exposed, the higher the preferred ratio of anionics to cationics. The proportions of materials within the concentrate compositions may also be described in terms of 7-30 weight percent anionic materials and 1-5 weight percent cationic materials. These percentages allow for a maximum range of about 30:1 to 1.28:1 ratios by weight of anionic materials to cationic materials. Unless otherwise stated, all proportion described in the examples are percentages by weight. FIG. 4 shows some of these interactive effects.

Additional ingredients that do not significantly and adversely affect the stability and lubricating properties of the composition may also be present in the compositions of the invention. Coupling agents, that is materials which have an affinity for both hydrophilic and hydrophobic materials may be included within the compositions. Coupling agents are also referred to as hydrotropes, chemicals which have the property of increasing the aqueous solubility of variously slightly soluble organic compounds. The compounds often have both hydrophilic and hydrophobic functionalities within a single molecule to display affinity to both environments, and are commonly used in the formulation of liquid detergents.

Another attribute of the present invention is that the lubricants of the invention tend to have a wider range of utility with respect to the container material and the conveyor material. It has usually been the practice in the art to specifically design lubricant compositions for use with particular container compositions and conveyor support materials. The supporting surfaces on conveyors may comprise fabric, metal, plastic, composite and mixtures of these materials. Lubricants would preferably be compatible with a variety of these surfaces. Similarly, bottle compositions may comprise metals, glasses, papers, treated papers, coated papers, laminates, ceramics, polymers, and composites, and the lubricant compositions would preferably have a range of compatibility with all of these materials. Although there may be some variation in the quality of performance with certain materials, the lubricants of the present invention do tend to display greater latitude in acceptable performance with a range of materials than many lubricant compositions.

Possible optional agents with high degrees of utility include chelating agents (e.g., EDTA), nonionic detergents, and alkalating agents, e.g., potassium, sodium hydroxide, or alkanolamines. The preferred chelating agents for use in the practice of the present invention are the amine-type acetic acids. These chelating agents typically include all of the poly(amine-type) chelating agents as described in U.S. Pat. No. 4,873,183. Other chelating agents such as nitrilotriacetic acid, alkali metal salts of glucoheptanoate, and organic substituted phosphoric acid, and their equivalents are also useful in the practice of the present invention. The chelating agents are preferably present as from 0.05 to 25% by weight of the lubricant concentrate composition, preferably from 0.05 to 15% by weight.

In a synthetic lubricant environment, the invention has found that quaternary ammonium antimicrobial agents, and especially the linear quaternary compounds act as lubricants in combination with the linear and phenol phosphate esters. At least one of the referenced art (e.g., PCT GB95/01641, page 17, lines 12-18) specifically shows that the combination of quaternary ammonium compounds with the alkyl (linear) phosphate esters did not affect lubricity. The finding that the combination of the quaternary ammonium antimicrobial agents with the combination of esters of the present invention actually increases lubricity (reduces the coefficient of friction) provides a basis for the assertion of unexpected results in the defined chemical classes of compounds.

______________________________________
Raw Material
Chemical Name (%)
______________________________________
Soft water 65.50
Phosphate Ester
C10-12 alkyl phosphate ester, 5 EO units
12.50
Rhodafac ™
phenol ethoxylated phosphate ester
2.50
RP-710
Bardac ™ 2250
didecyl dimethyl ammonium chloride, 50%
5.00
Versene ™ 100
EDTA, 40% 10.00
NaOH, 50% NaOH 2.00
Neodol ™ 25-7
C12-15 linear alcohol, 7 EO
2.50
100.00
______________________________________

Two formulae were prepared as set out below. The first formula contained the blended phosphate esters, EDTA, NaOH, and linear quaternary ammonium antimicrobial agent. The second formula was identical with the exception of the linear quat.

0.1% use solutions of each formula were prepared in softened water. This solution was sprayed on the short track conveyor which was set up with glass bottles held stationary as the stainless steel conveyor rotated at 100 rpm. The drag was measured with a load cell, which was in turn connected to a computer which plotted the COF (kinetic) based on the drag and the load. The results are presented below in FIG. 1, a graph displaying the coefficient of friction (COF) versus time for a phosphate ester with a linear quat versus a phosphate ester used alone.

______________________________________
Formula
(%)
Raw Material
Chemical Name 10-1 10-2
______________________________________
Soft Water 68.0 73.0
PE C10-12 alkyl phosphate ester,
12.5 12.5
5 EO units
RP-710 phenol ethoxylated phosphate ester
2.5 2.5
Versene ™ 100
EDTA, 40% 10.0 10.0
NaOH NaOH 2.0 2.0
Bardac ™ 2250
didecyl dimethyl ammonium
5.0 0.0
chloride, 50%
100.0 100.0
______________________________________

The inclusion of linear quat in the formula improves the lubricity over a lubricant containing only the blend of phosphate esters.

Two formulas of lubricating agents were prepared as set out below. The first formula contained the blended phosphate esters, EDTA, NaOH, nonionic surfactant, and linear quaternary ammonium antimicrobial agent. In the second formula, the linear quaternary ammonium antimicrobial agent was replaced with benzyl quat.

0.1% use solutions of each formula were prepared in softened water. This solution was sprayed on the short track conveyor that was set up with glass bottles held stationary as the stainless steel conveyor rotated at 100 rpm. The drag was measured with a load cell, which was in turn connected to a computer, which plotted the COF (kinetic) based on the drag and the load. The results are presented in FIG. 2 which shows a comparison of COF versus time for phosphate esters with either a linear quat or a benzyl quat.

______________________________________
Formula
(%)
Raw Material
Chemical Name KX 10-3
______________________________________
Soft Water 68.0 68.0
PE C10-12 alkyl phosphate ester,
12.5 12.5
5 EO units
RP-710 Phenol ethoxylated phosphate ester
2.5 2.5
Versene ™ 100
EDTA, 40% 10.0 10.0
NaOH NaOH 2.0 2.0
Bardac ™ 2250
didecyl dimethyl ammonium
5.0 0.0
chloride, 50%
Q-372 benzyl quat, 50% 0.0 5.0
(a mixture of alkyldimethyl-
benzyl ammonium chlorides)
100.0 100.0
______________________________________

The linear quat species improves the lubricity of the formula as compared to the benzyl quat.

Two formulae were prepared as set out below. The first formula contained blended alkyl and aryl phosphate esters and the second formula contained only alkyl phosphate ester. Both formulas contained EDTA, nonionic, NaOH, and linear quat.

The viscosity of the concentrates was measured in triplicate on a Brookfield viscometer model RVT at 51°, 78° and 116° F. (spindle #3, 100 rpm, factor=10). The results are provided below.

______________________________________
Formula
Raw Material
Chemical Name (%)
______________________________________
Soft Water 65.50 65.50
PE C10-12 alkyl phosphate ester,
15.00 12.50
5 EO units
Versene ™ 100
EDTA, 40% 10.00 10.00
NaOH, 50% NaOH 2.00 2.00
Bardac ™ 2250
didecyl dimethyl ammonium
5.00 5.00
chloride, 50%
Neodol ™ 25-7
C12-15 linear alcohol, 7 EO
2.50 2.50
Rhodafac ™
phenol ethoxylated phosphate
2.50
RP-710 ester
100.00 100.00
______________________________________
______________________________________
Temperature Average Viscosity
(°F.)
Phosphate Ester(s)
(cps)
______________________________________
51 Alkyl and Phenol blend
50
78 Alkyl and Phenol blend
51
116 Alkyl and Phenol blend
49
51 Alkyl 170
78 Alkyl 132
116 Alkyl 64
______________________________________

Blending phenol phosphate ester with alkyl phosphate ester in the formula reduces the viscosity at all temperatures tested and the resultant low viscosity appears to be temperature independent. This property provides for ease of application on a conventional conveyor apparatus.

Formulas containing alkyl phosphate ester and linear quat were prepared with various nonionic and anionic adjuvants to determine the affect on lubricity. A control containing phenol phosphate ester, a control with higher level of alkyl phosphate ester, and a control with no adjuvant were prepared for comparative purposes. The formulas are provided below.

0.1% use solutions of each formula were prepared in softened water. This solution was sprayed on the short track conveyor which was set up with glass bottles held stationary as the stainless steel conveyor rotated at 100 rpm. The drag was measured with a load cell, which was in turn connected to a computer which plotted the coefficient of friction (COF) based on the drag and the load. Each sample was run two or more times, and the average COF was calculated. The results are provided in Table A below.

TABLE A
__________________________________________________________________________
Formulas
Raw Material
Chemical Name
1 2 3 4 5 6 7
__________________________________________________________________________
Soft Water above 68.00
65.50
61.70
65.50
65.50
65.50
65.50
PE-362 above 12.50
15.00
12.50
12.50
12.50
12.50
12.50
Versene ™ 100
above 10.00
10.00
10.00
10.00
10.00
10.00
10.00
NaOH, 50% above 2.00
2.00
2.00
2.00
2.00
2.00
2.00
Bardac ™ 2250
above 5.00
5.00
5.00
5.00
5.00
5.00
5.00
Neodol ™ 25-7
above 2.50
2.50
2.50
2.50
2.50
2.50
2.50
SXS, 40% Na xylene Sulfonate
6.30
Rhodafac ™ RP-710
above 2.50
Polysorbate ™ 80
sorbitan monooleate 2.50
Glucopan ™ 625CSUP
Alkyl poly glycoside 2.50
TritonTM X-102
Octylphenol 2.50
ethoxylate
__________________________________________________________________________

The phenol and alkyl phosphate esters improved lubricity over the control, while none of the other adjuvants showed this advantage.

This example examines the ratios of phosphate ester and quat which do not interact with beverage to form a precipitate. A 40% phosphate ester solution in soft water was combined with 10% active linear quat solution in water and a cola beverage at various levels. After one day, the samples were observed for clarity. Samples were rated as clear, hazy, and separated. (Over time, all hazy samples formed precipitates.)

See the ternary plot in FIG. 4.

At higher levels of beverage a higher ratio of anionic to cationic surfactant is required to maintain clarity. The ratio ranges from about 1.5:1 at very low levels of beverage, to 2.5:1 at 50% beverage and 16:1 at very high levels of beverage.

______________________________________
Time
(min)
X-102 Poly-80 Gluc SXS Control
RP-710
PE-362
______________________________________
20 0.1435 0.14405 0.14135
0.1339
0.1343
0.12986
0.1288
20.5 0.14435 0.14215 0.14135
0.13385
0.13335
0.12948
0.12915
21 0.14445 0.1424 0.14085
0.13415
0.13295
0.12968
0.1289
21.5 0.14355 0.1424 0.14025
0.1334
0.13215
0.12978
0.12895
22 0.1443 0.14375 0.14065
0.1337
0.1327
0.1296
0.12895
22.5 0.1433 0.1435 0.1412
0.1333
0.13315
0.1295
0.1299
23 0.144 0.1424 0.14115
0.1342
0.13345
0.12976
0.1294
23.5 0.14415 0.1415 0.14125
0.13355
0.1329
0.13014
0.12915
24 0.1441 0.14095 0.14045
0.1333
0.13255
0.13012
0.1287
24.5 0.14385 0.14135 0.13985
0.13315
0.13325
0.13014
0.1291
25 0.14285 0.14245 0.1396
0.13335
0.1339
0.12926
0.1289
25.5 0.14325 0.1417 0.1399
0.1337
0.133 0.12982
0.129
26 0.14405 0.1422 0.13985
0.1334
0.13235
0.1296
0.1287
26.5 0.14385 0.1415 0.13955
0.13425
0.1324
0.12986
0.12865
27 0.14485 0.14085 0.13975
0.1336
0.1324
0.12976
0.12805
27.5 0.1434 0.1409 0.1398
0.1334
0.13275
0.12914
0.12875
28 0.14295 0.1411 0.1391
0.1324
0.13275
0.12946
0.12935
28.5 0.14385 0.1408 0.13895
0.1322
0.13245
0.12936
0.1294
29 0.144 0.141 0.13835
0.13295
0.1327
0.12946
0.1293
29.5 0.1435 0.14115 0.13965
0.1333
0.13345
0.12892
0.12935
30 0.1433 0.14065 0.13895
0.13315
0.1329
0.12916
0.1291
30.5 0.14265 0.1408 0.1393
0.13355
0.1333
0.12916
0.12945
31 0.14265 0.14065 0.1397
0.13285
0.1335
0.12912
0.1289
31.5 0.14255 0.14105 0.1391
0.1322
0.13245
0.12938
0.1284
32 0.14385 0.1401 0.13905
0.1323
0.132 0.1299
0.1291
32.5 0.142 0.1405 0.13855
0.13265
0.1332
0.12892
0.1289
33 0.14275 0.13985 0.13785
0.13365
0.1354
0.1288
0.12905
33.5 0.14175 0.1398 0.1388
0.13345
0.13505
0.12872
0.12935
34 0.14215 0.1401 0.13835
0.1338
0.135 0.12922
0.1293
34.5 0.14255 0.14105 0.139 0.13195
0.1367
0.12938
0.12925
35 0.14135 0.1407 0.1387
0.1326
0.13675
0.12904
0.1294
______________________________________
______________________________________
Elapsed Minutes PE + Quat
PE
______________________________________
0.5 0.197 0.1912
1 0.1956 0.1912
1.5 0.1948 0.1908
2 0.1938 0.1905
2.5 0.1929 0.1903
3 0.2106 0.2174
3.5 0.1969 0.2046
4 0.1702 0.1794
4.5 0.1605 0.1663
5 0.1531 0.158
5.5 0.1469 0.1518
6 0.1436 0.148
6.5 0.1412 0.1439
7 0.1388 0.1421
7.5 0.1365 0.1401
8 0.1345 0.1389
8.5 0.1336 0.1371
9 0.132 0.1362
9.5 0.1304 0.1359
10 0.1307 0.1354
10.5 0.1296 0.135
11 0.1297 0.1345
11.5 0.13 0.1332
12 0.1298 0.1342
12.5 0.1301 0.1339
13 0.1288 0.1337
13.5 0.1282 0.1335
14 0.1262 0.134
14.5 0.1253 0.1352
15 0.1252 0.1364
15.5 0.1252 0.1363
16 0.125 0.1377
16.5 0.1243 0.1391
17 0.1245 0.1395
17.5 0.1246 0.1431
18 0.1244 0.1435
18.5 0.1247 0.1426
19 0.1234 0.1442
19.5 0.1243 0.1454
20 0.1239 0.147
20.5 0.1239 0.1484
21 0.1241 0.1487
21.5 0.1235 0.1485
22 0.1229 0.1474
22.5 0.1243 0.1469
23 0.1233 0.1476
23.5 0.1225 0.1474
24 0.1237 0.1474
24.5 0.123 0.1474
25 0.124 0.1474
25.5 0.1238 0.1494
26 0.1235 0.1482
26.5 0.1257 0.1477
27 0.1261 0.147
27.5 0.1254 0.1451
28 0.1259 0.1454
28.5 0.1225 0.1463
29 0.1228 0.1469
29.5 0.1226 0.1489
30 0.1227 0.1485
30.5 0.1231 0.1486
31 0.1226 0.1483
31.5 0.1232 0.1471
32 0.1241 0.1472
32.5 0.1237 0.1478
33 0.1232 0.1488
33.5 0.1236 0.1485
34 0.1232 0.1493
34.5 0.1241 0.1486
35 0.1236 0.1502
______________________________________

Besse, Michael E., Person Hei, Kimberly L., Dressel, Joy G.

Patent Priority Assignee Title
Patent Priority Assignee Title
2779740,
3382032,
3645897,
3860521,
4419253, Nov 06 1981 NALCO CHEMICAL COMPANY, A OAK BROOK, ILL A DE CORP Synthetic post-pickle fluid
4521321, May 03 1982 Diversey Wyandotte Inc. Conveyor track lubricant composition employing phosphate esters and method of using same
4557848, Dec 08 1983 Texaco Inc. Crankcase lubricant
4604220, Nov 15 1984 DIVERSEY IP INTERNATIONAL BV Alpha olefin sulfonates as conveyor lubricants
4636321, Sep 30 1985 Reynolds Metals Company Water soluble lubricant
4758359, Feb 13 1987 Reynolds Metals Company Aqueous metal working lubricant containing a complex phosphate ester
4839067, Sep 19 1986 JOHNSONDIVERSEY, INC Process for lubricating and cleaning of bottle conveyor belts in the beverage industry
5062979, Sep 16 1988 Ecolab USA Inc Soap free conveyor lubricant that gives clear solutions in water comprising alkoxyphosphate ester, alkyl benzene sulfonate and carboxylic acid
5073280, Jul 14 1988 DIVERSEY IP INTERNATIONAL BV Composition for inhibiting stress cracks in plastic articles and methods of use therefor
5182035, Jan 16 1991 Ecolab USA Inc Antimicrobial lubricant composition containing a diamine acetate
5190679, Mar 14 1991 AMERICAN POLYWATER CORPORATION A CORP OF MN Aqueous based loosener composition adapted for removing cable from a conduit
5223162, Jul 14 1988 DIVERSEY, INC Washing composition for inhibiting stress cracking in poly(alkylene terephthalate) articles and methods of use therefor
5282992, Apr 07 1992 BETZDEARBORN INC Lubricating metal cleaner additive
5352376, Feb 19 1993 Ecolab USA Inc Thermoplastic compatible conveyor lubricant
5391308, Mar 08 1993 Ecolab USA Inc Lubricant for transport of P.E.T. containers
5407700, Sep 15 1993 Ecolab USA Inc Food safe composition to facilitate soil removal
5409713, Mar 17 1993 Ecolab USA Inc Process for inhibition of microbial growth in aqueous transport streams
5419908, Jun 04 1991 Ecolab Inc. Sanitizing composition comprising a blend of aromatic and polyunsaturated carboxylic acids
5436008, Dec 11 1992 Ecolab USA Inc Sanitizing compositions
5437868, Jul 23 1991 Ecolab USA Inc Peroxyacid antimicrobial composition
5441654, Jul 14 1988 DIVERSEY IP INTERNATIONAL BV Composition for inhibiting stress cracks in plastic articles and methods of use therefor
5462681, Nov 12 1993 Ecolab USA Inc Particulate suspending antimicrobial additives
5489434, Jul 23 1991 Ecolab USA Inc Peroxyacid antimicrobail composition
5510045, Jul 14 1988 DIVERSEY IP INTERNATIONAL BV Alkaline diamine track lubricants
5667349, Apr 26 1995 VALENITE U S A INC Method of making pull tabs and lubricant therefor
FR533552,
JP2097592,
JP2097593,
JP734079,
JP8333592,
WO9602616,
/
Executed onAssignorAssigneeConveyanceFrameReelDoc
Jan 05 1998Ecolab Inc(assignment on the face of the patent)
Date Maintenance Fee Events


Date Maintenance Schedule
Jan 26 20024 years fee payment window open
Jul 26 20026 months grace period start (w surcharge)
Jan 26 2003patent expiry (for year 4)
Jan 26 20052 years to revive unintentionally abandoned end. (for year 4)
Jan 26 20068 years fee payment window open
Jul 26 20066 months grace period start (w surcharge)
Jan 26 2007patent expiry (for year 8)
Jan 26 20092 years to revive unintentionally abandoned end. (for year 8)
Jan 26 201012 years fee payment window open
Jul 26 20106 months grace period start (w surcharge)
Jan 26 2011patent expiry (for year 12)
Jan 26 20132 years to revive unintentionally abandoned end. (for year 12)