[0001] This invention relates to aqueous lubricant compositions suitable for use in the
beverage and food industries.
[0002] In the beverage and food industries product containers, such as bottles or cans,
are commonly transported on continuously operating conveyors through unit operation
stations, such as filling, closure or sealing stations. During transport between the
stations, or at each operation, blockages of the containers on the conveyor can occur
while the conveyor continues to move. To cope with these interruptions and resumptions
in the movement of the containers reliably a low but appreciable sliding friction
between the material of the containers and of the conveyor is required. It is usual
to use a lubricant on the conveyor to achieve the required frictional characteristics.
Additional functions of a lubricant are to provide control of microbiological growth
and to provide detergency to remove spillages and other soils.
[0003] While the present invention has broad applicability to the conveyance of containers
it is envisaged to be particularly applicable to the conveyance of glass, plastic,
plastic impregnated or coated cardboard, or metal beverage containers on belt or chain
conveyors of metal or plastic. When the container is of glass a stainless steel conveyor
is often used whereas, when the container is of another material, for example of aluminium,
or of polyethylene terephthalate (PET) or of polyethylene (PE) the conveyor may be
of, for example, of nylon or of polypropylene or an acetal resin.
[0004] Lubricant compositions are also subject to requirements other than those relating
purely to their frictional performance. Some lubricant compositions, for example those
based on fatty acids, react with the hardness salts in water to deposit alkaline earth
fatty acid salts on the conveyor and on the pipework used to deliver lubricant to
the conveyor. This may be alleviated by ensuring that only soft water, for example
containing hardness salts equivalent to below 5 ppm CaCO
3, is used to make up the lubricant or by including an effective amount of a complexing
agent, such as ethylene diamine tetra-acetic acid (EDTA), in the composition. Some
lubricant compositions, for example those based on fatty amines, may tend to cause
stress-cracking in the bases of plastic containers, such as PET containers, under
conditions of internal pressurisation and/or warming. Using the lubricant compositions
of the invention this effect may be reduced. Some lubricant compositions amongst the
fatty acid-, fatty amine- and phosphate ester-based compositions have a deleterious
effect on print and tend to cause the leaching of printing ink from a print display.
Since it is common practice to preprint beverage cans this presents a considerable
problem.
[0005] U.S. patent specification No. 5 747 431 describes an aqueous lubricant composition
containing one or more of a specific range of cyclic imidazolines defined by general
formula and an amount of an inorganic acid or a carboxylic acid having up to 6 carbon
atoms, for example acetic acid, sufficient to render the cyclic imidazoline soluble
in water. The quantity of the acid is typically from 0.05 to 10.5% by weight of the
concentrate and, if required, additional acid is be added to bring the pH into the
required region which is, preferably, from 3 to 8, more preferably from 3 to 6. At
such a pH the imidazoline is solubilized by conversion to the acetate. Optionally,
the lubricant composition may also contain an alkylamine carboxylate although this
is exemplified in a quantity of only 0.6% wt/wt active raw material relative to 2.0%
on an active basis, of the imidazoline.
[0006] U.K. patent specification No. 2 285 630-A describes an aqueous lubricant composition
containing an alkylamine dicarboxylate, a cyclic imidazoline and an alkyl sulphonate
anionic surfactant, each defined by general formula.
[0007] The present invention, in its broadest aspect, is based on an aqueous lubricant composition
comprising a combination of an amphoteric carboxylate with an imidazoline, the composition
having a pH greater than 8, and on the finding that an unexpected degree of reduction
in sliding friction obtainable by the use of such a composition, as well as certain
other beneficial properties, in the absence of a content of any effective quantity
of an anionic sulphonate surfactant, or of any other anionic surfactant. For example,
any sulphonate or other anionic surfactant, if present, is preferably present in less
than 0.2%, particularly preferably less than 0.15% by weight of the composition.
[0008] In defining the composition provided by the invention it is noted that cyclic imidazolines
are believed to hydrolyse under some pH conditions with ring opening. The present
invention encompasses both cyclic imidazolines and the chain compounds corresponding
to the cyclic imidazoline hydrolysis products, whether the chain compounds are actually
formed by the hydrolysis mechanism or not, or whether they are formed in situ in the
lubricant composition or not and the term "hydrolysis product", used hereafter, is
intended to encompass all of these alternative possibilities.
[0009] The present invention provides an aqueous lubricant composition comprising a combination
of (a) one or more alkylamine monocarboxylates defined by the general formula (I)
wherein
R1 represents C1 to C24, preferably C7 to C24, alkyl- or C1 to C24, preferably C7 to C24, alkyl-[N-(CH2)n']m- wherein n,n' and m are the same or different and have values of at least 1, preferably
from 1 to 5
R2 represents H, C1 to C24 alkyl or C1 to C24 alkyl substituted by one or more hydroxyl or amine groups
M+ represents H+, Na+, K+ or (CH2OH.CH2)3NH+
and (b)
one or more cyclic imidazolines defined by the general formula (II), and hydrolysis
products thereof,
wherein
R4 is -CH2-CH2-OH or -CH2-CH2-NH2 or is an amide function
R5 is an alkyl chain having a value of at least C1, preferably from C1 to C30.
[0010] The preferred compounds within Formula (I) for use in the practice of the present
invention are:
wherein R
3 is an alkyl fatty chain, preferably of coco-distribution.
[0011] The preferred compounds within Formula (II) for use in the practice of the present
invention are:
and hydrolysis products thereof.
[0012] The lubricant compositions of the invention may be in the form of a concentrate,
for example containing from 0.1% to 10% by weight, or up to the solubility limit,
which may be up to 20% by weight or more, in total and on an active material basis,
of the amphoteric alkyl carboxylate and the imidazoline. Such a concentrate is preferably,
but not essentially, produced using naturally soft water, distilled water or softened
water to maximise storage stability. For use the concentrate is further diluted, for
example from 0.0005% to 5%, preferably at least 0.005%, preferably up to 2%, in total
and on the same basis, of the same compounds. For this further dilution it is found
that soft, medium or even hard water may be used. The relative molar proportion of
the amphoteric alkyl carboxylate and the imidazoline is preferably from 10:90 to 90:10,
particularly preferably from 60:40 to 40:60.
[0013] The lubricant compositions may contain other constituents, for example a hydrophilic
organic co-solvent such as, for example butyl diglycol, monoethylene glycol or isopropyl
alcohol, suitably in a concentration of from 1% to 10% by weight, a nonionic surfactant
such as an alcohol alkoxylate, suitably in a concentration of 0.1% to 5% by weight
and a biocide, suitably in a concentration of from 0.1% to 10% by weight. The cosolvent
may be supplied by using the amphoteric carboxylate in the form of a solution thereof.
[0014] Preferably, to enhance solubility, the pH of the lubricant composition of the invention
is controlled at a pH greater than 8.5 for example, desirably, greater than 9. It
is preferred that the pH is below 11 and a pH range of from 9.5 to 10.5 is particularly
preferred. At the pH levels envisaged by this invention the imidazoline is, surprisingly,
solubilized in the presence of the alkylamine carboxylate. There is no reliance on
salt formation to achieve solution in water.
[0015] The effectiveness of the lubricant compositions may be tested as follows.
Lubrication.
[0016] A number of glass bottles sufficient to give a load of 2000g are placed on a pilot
conveyor fitted with a stainless steel track. The bottles are tethered to a force
gauge capable of measuring the drag force in grams. Lubricant at a suitable concentration
is sprayed onto the track and the track set in motion. Drag Coefficient (U) is calculated
as Drag Force/2000 g. A coefficient of less than 0.15 represents good lubrication
and higher values represent poor lubrication.
PET Compatibility.
[0017] Pressurised PET bottles are dipped into a sample of lubricant prediluted to use concentration
(typically 1% by weight). After 10 minutes the bottles are removed and placed in an
oven at a temperature of 38°C. After 72 hours at this temperature the bottles are
removed and are examined visually for signs of stress cracking. A bottle similarly
oven treated, which had not been contacted with the lubricant is used as a control.
Ink compatibility.
[0018] Samples of steel sheet printed with a representative ink are immersed in solutions
of the lubricant having up to 10 times normal use concentration. The solutions are
held at a temperature of 60°C for 30 minutes and the samples were then removed and
examined visually for ink leaching.
[0019] Certain lubricant compositions according to the invention are now described with
reference to the following examples but without any limitation of the scope of the
invention thereto. Examples 1, 4 and 5 are according to the invention and Examples
2 and 3 are not according to the invention but are comparative therewith.
Examples 1-3.
[0020] The following compositions were made up by adding the other ingredients to the water
and the compositions were tested for Drag Coefficient at a dilution of 1% by weight
in tap water.
Example No. |
1 |
2 |
3 |
Distilled water |
85 |
87 |
90 |
Butyl diglycol |
2 |
2 |
2 |
Nonionic alcohol alkoxylatea |
2 |
2 |
2 |
Amphotericb |
2.5 |
2.5 |
2.5 |
Biocidec |
1.5 |
1.5 |
1.5 |
Imidazolined |
2 |
0 |
2 |
Amphoteric alkyl amine |
|
|
|
carboxylatee |
5 |
5 |
0 |
|
pH |
10 |
9 |
11 |
|
Drag Coefficient |
0.075 |
0.1 |
0.15 |
Trade names/sources of constituents
a Synperonic LFRA30 - ICI. |
b Amphoteric SBF - Rhone Poulenc. |
c Bioban CS 1135 - Angus Chemicals. |
d R5 (formula IV) - Lakeland Laboratories |
e Amphoran CP1 - Formula (III) with R3 = coco-. - Elf Atochem. |
[0021] Example 1 used both the essential components of the invention, the imidazoline was
absent from Example 2 and the amphoteric alkyl amine carboxylate was absent from Example
3. A synergic effect is apparent in the composition according to the invention from
the results.
Examples 4-5.
[0022] The following compositions were made up and tested for Drag Coefficient at a dilution
of 0.5% by weight in tap water.
Example No. |
4 |
5 |
Distilled water |
89 |
89 |
Nonionic alcohol alkoxylatef |
0.5 |
0.5 |
Biocideg |
4 |
4 |
Imidazolineh 80H (R5 = C8) |
1.5 |
0 |
Imidazolineh120H (R5 = C12) |
0 |
1.5 |
Amphoteric alkyl amine |
|
|
carboxylatej |
5 |
5 |
|
pH |
10 |
10 |
|
Drag Coefficient |
0.11 |
0.11 |
Trade names/sources of constituents |
f Synperonic NCA810 - ICI |
g Emulcid - Thor Chemicals |
h Lakeland Laboratories |
j Amphoram |
[0023] These Examples show no difference between the Imidazolines having chains of 8 and
of 12 carbon atoms. This is surprising since the longer chain length (C
12 to C
18) has traditionally been preferred.
Variations in the Examples.
[0024] The Example 4 composition was further diluted to 1% in water containing 10ppm sulphate
or 10ppm phosphate ions. Both solutions remained clear overnight. This is in contrast
to cationic lubricants, such as those based on fatty amines, which tend to become
cloudy on standing as a result of the formation of insoluble sulphate or phosphate
salts.
[0025] The Example 5 composition, further diluted to 1% by weight, was tested in waters
ranging from 30 to 250 ppm CaCO
3 of hardness with no observable difference in Drag Coefficient. All the solutions
remained clear despite the absence of a chelating agent.
Other tests.
[0026] Using the test methods given above lubricant compositions of the invention were found
to be compatible with Can Print Pigments and PET.
[0027] Experiments were conducted using other surfactant acids including sarcosinates, phosphate
esters, ether carboxylates and sulphonic acids. The are less effective in that either
the formulations are not hard water stable, have poor lubrication or have poor stability.
However, it is likely that stability could be improved by the use of suitable cosolvents
or surfactants.
[0028] A solution containing 1.5% by weight of Imidazoline 80H and 98.5% by weight of butyl
diglycol was made up. It was found to have a pH of 10.5 which is very close to the
pH levels in the preceding Examples. This is taken to indicate that the imidazoline
is present in a similar form in the Examples as in the present test.
1. An aqueous lubricant composition, suitable for conveyor lubrication in the beverage
or food industries, comprising a combination of an amphoteric carboxylate and an imidazoline,
the composition having a pH above 8 and being in the absence of any effective quantity
of an anionic sulphonate surfactant.
2. A composition as claimed in claim 1 wherein the carboxylate is an amphoteric alkyl
amine carboxylate.
3. A composition as claimed in claim 2 wherein the carboxylate is a monocarboxylate.
4. An aqueous lubricant composition, suitable for conveyor lubrication in the beverage
or food industries, comprising a combination of
(a) one or more alkylamine monocarboxylates defined by the general formula (I)
wherein
R1 represents C1 to C24, preferably C7 to C24, alkyl- or C1 to C24, preferably C7 to C24, alkyl-[N-(CH2)n']m- wherein n, n' and m are the same or different and have values of at least 1, preferably
from 1 to 5.
R2 represents H, C1 to C24 alkyl or C1 to C24 alkyl substituted by one or more hydroxyl or amine groups
M+ represents H+, Na+, K+ or (CH2OH.CH2)3NH+ and
(b) one or more cyclic imidazolines defined by the general formula (II), and hydrolysis
products thereof ,
wherein
R4 is - CH2-CH2-OH or -CH2-CH2-NH2 or is an amide function
R5 is an alkyl chain having a value of at least C1, preferably from C1 to C30.
the composition having a pH above 8.
5. A composition as claimed in claim 4 wherein the one or more alkylamine monocarboxylates
is as defined by formula (III)
6. A composition as claimed in claim 4 wherein the one or more imidazolines is as defined
by formula (IV)
and hydrolysis products thereof.
7. A composition as claimed in any preceding claim in the form of a concentrate containing
from 0.1% by weight, to the solubility limit, in total and on an active material basis
of the amphoteric carboxylate and the imidazoline.
8. A composition as claimed in any preceding claim in the form of a working solution
containing from 0.0005% to 5% by weight, in total and on an active material basis,
of the amphoteric carboxylate and the imidazoline.
9. A composition as claimed in any preceding claim containing the amphoteric carboxylate
and the imidazoline in relative molar proportions of from 10:90 to 90:10.
10. A composition as claimed in any preceding claim having a pH greater than 8.5.
11. A composition as claimed in claim 10 having a pH from 9.5 to 10.5.
12. A composition as claimed in any preceding claim containing one or more of a hydrophilic
organic co-solvent in a concentration of from 1% to 10% by weight, a nonionic surfactant
in a concentration of 0.1% to 5% by weight and a biocide, in a concentration of from
0.1% to 10% by weight.
13. The use of a composition as claimed in any preceding claim in conveyor lubrication.
14. The use claimed in claim 13 wherein the conveyor is of stainless steel, polypropylene
or an acetal resin and the containers to be conveyed are of glass, aluminium, steel,
polyethylene terephthalate(PET), polyethylene(PE) or cardboard.