Technical field
[0001] The present invention refers to a method for lubricating conveyor systems consisting
of applying a lubricant composition wherein the active matter concentration of said
lubricant composition ranges from 1 to 99% by weight. Said method is particularly
preferred in conveyor systems for glass bottles, plastic bottles such as polyethylene
terephtalate (PET) or polycarbonate (PC) bottles, cans, glass containers and cartons
containers and similar items. Said conveyor systems can particularly be found in the
foodstuff industry.
Prior Art
[0002] Usually, in bottle and barrel plants of drinks' manufacturers and in food packaging,
articulated plate conveyor belts or other transport systems are used. Said systems
are maintained lubricated to reduce the mechanical strength of the bottles and containers,
and cleaned to remove dirt and to avoid contamination by micro-organisms, with the
aid of appropriate aqueous lubricating agents, preferentially applied with automatic
lubrication systems for conveyor belts or other transport systems, equipped with a
sprayer system.
[0003] Typically, a lubricant concentrated composition is diluted with water to form a lubricant
diluted composition (i.e., dilution factors of 2 to 10000, preferably 5 to 1000 by
volume), and copious amounts of lubricant diluted compositions are typically applied
to the conveyor systems or containers using spray or pumping equipment on a continuous
basis. The lubricant diluted composition can be collected in drip trays, which discharge
into drainage systems and then to the effluent plant for disposals.
[0004] These lubricant diluted compositions permit high-speed operation of the conveyor
system and limit marring of the containers or labels, but also have some disadvantages:
- The high quantity of water required on the conveying line (a normal lubrication spray
nozzle has a capacity of 5 L/min; with a 50% spray and 50% pause time, each nozzle
uses 2.5 L of lubricant diluted compositions per hour)
- Spillages on floors caused by frothing of the lubricant diluted compositions result
in hazardous working conditions and slippery floors around the packaging lines.
- Some lubricant diluted compositions can promote the growth of microorganisms, which
has to be prevented by using biocides.
- The lubricant diluted composition, which has been collected in drip trays, has to
be treated in the effluent treatment plants before disposal. However, the presence
of biocides may affect the bacteria in the wastewater treatment facilities.
- By requiring dilution of the lubricant concentrated dilution errors can occur, leading
to variations and errors in concentration of the lubricant diluted solution.
- By requiring water from the plant, variations in the water can have negative side
effects on the lubricant diluted composition. For example, alkalinity in the water
can lead to environmental stress cracking in PET bottles.
[0005] "Dry lubricants" have been described as a solution to the disadvantages of the diluted
lubricant compositions. A "dry lubricant" historically has referred to a lubricant
composition with low water content, preferably less than 50 wt.%, which was applied
to a container or conveyor system without dilution. However, this application typically
required special dispensing equipment and nozzles and energized nozzles in particular.
Energized nozzles refer to nozzles where the lubricant stream is broken into a spray
of fine droplets by the use of energy, which may include high pressures, compressed
air, or sonication to deliver the lubricant.
[0006] Dry lubricants based on silicone materials and/or polymers (i.e. Teflon) are very
common. However, silicone is primarily effective at lubricating plastics such as PET
bottles, and has been observed to be less effective at lubricating on glass or metal
containers, particularly on a metal surface. If a plant is running more than one type
of container on a line, the conveyor lubricant will have to be switched before the
new type of container can be run. Alternatively, if a plant is running different types
of containers on different lines, the plant will have to stock more than one type
of conveyor lubricant. Both scenarios are time consuming and inefficient for the plant.
[0007] Furthermore, silicone materials and certain polymers are not biodegradable and may
contaminate the effluents.
[0008] In the applicant's International patent application
PCT/EP2007/002772, which is awaiting publication and which is hereby incorporated by reference, a description
is given of lubricant compositions comprising, expressed as weight percentage,
- a) 10-85% of one or more phosphoric acid esters;
- b) 5-60% of one or more ether carboxylates;
- c) 0.1-30% of one or more C6-C22 fatty acids, optionally ethoxylated with 1 to 20 moles of ethylene oxide;
- d) 0.1-30% of one or more C6-C22 fatty alcohols, optionally ethoxylated with 1 to 20 moles of ethylene oxide; and
- e) water add up to 100%.
[0009] Said International patent application describes both concentrated and diluted lubricant
compositions, which are obtained by diluting the previous lubricant concentrated compositions.
Furthermore, said European patent application also describes a method for lubricating
conveyor systems consisting in applying a lubricant diluted composition (0.03% by
weight) obtained by diluting the lubricant concentrated composition described above
to a conveyor system. The use of the lubricant diluted composition for lubricating
conveyor systems is also described.
[0010] Said dilution can be carried out either directly in one step or through intermediate
partially diluted compositions, i.e. starting from a concentrate, diluting it by a
factor of 2 to 100, and finally diluting it again to the desirable final concentration.
This procedure is commonly used to avoid transport and storage of highly diluted compositions.
[0011] It can be concluded that the industry still requires improvements in the field of
lubricating conveyor systems by applying lubricant non-diluted compositions, which
avoids the drawbacks mentioned before and which allows applied to different materials
(glass, PET, cans, etc.) being more versatile.
Summary of the invention
[0012] The authors of the present invention have surprisingly found that, the lubricant
compositions described in the International patent application
PCT/EP2007/002772, if applied directly or in the form of partially diluted compositions, wherein the
active matter concentration of the lubricant composition ranging from 1 to 99% by
weight, to conveyor systems, not only provide appropriate lubricant properties, but
also provide an efficient solution to the problems mentioned before: said composition
can be applied without further dilution with standard application equipments (i.e.
non-energized nozzles) resulting in drier lubrication of the conveyor systems and
drier conveyor line and working area, reduced lubricant usage, reduced waste, cleanup
and disposal problems, and avoiding dilution problems.
[0013] Furthermore, said lubricant compositions have a better ecotoxicological profile than
existing concentrated (dry) lubricant compositions based on silicone materials and/or
polymers.
[0014] Thus, the present invention provides a method for lubricating conveyor systems consisting
of applying, continuously or at intervals, a lubricant composition comprising the
following essential elements,
- a) one or more phosphoric acid esters of formula (I)

wherein
- R1 represents a linear or branched, saturated or unsaturated C6-C22 alkyl and/or alkenyl group, or a R3(OCH2CH2)m group;
- R2 represents hydrogen, a linear or branched, saturated or unsaturated C6-C22 alkyl and/or alkenyl group, or a R3(OCH2CH2)m group;
- R3 represents hydrogen or a linear or branched, saturated or unsaturated C6-C22 alkyl and/or alkenyl group;
- m represents a number of from 1 to 15; and
- Z represents hydrogen or an appropriate cation
- b) one or more ether carboxylates of formula (II)
R-O-(CH2CH2O)n-CH2COOM (II)
wherein
- R represents a linear or branched, saturated or unsaturated C6-C22 alkyl and/or alkenyl group;
- n represents a number of from 0.5 to 20, and
- M represents hydrogen or an appropriate cation, selected from the group consisting
of an alkali metal, an alkaline earth metal, ammonium, an alkylammonium, an alkanolammonium
or a glucammonium; and
- c) one or more C6-C22 fatty acids, optionally ethoxylated with 1 to 20 moles of ethylene oxide; and
- d) one or more C6-C22 fatty alcohols, optionally ethoxylated with 1 to 20 moles of ethylene oxide;
- e) an inert solvent or mixture thereof,
wherein the active matter concentration of said lubricant composition ranges from
1 to 99% by weight.
[0015] The present invention also provides the use of the lubricant composition defined
above for lubricating conveyor systems.
Detailed description of the invention
The phosphoric acid esters
[0016] The phosphoric acid esters of formula (I) may be prepared by reacting in aqueous
media C
6-C
22 fatty alcohols with phosphorous pentoxide (P
2O
5).
[0017] The C
6-C
22 fatty alcohols are preferably derived from natural fat and oil as well as synthetic
origin. Preferred fats and oils include palm oil, coconut oil, sunflower oil, rapeseed
oil, castor oil, olive oil, soybean oil; and animal fat such as tallow, bone oil;
fish oil, hardened oils and semihardened oils thereof; and mixtures thereof. As a
result of its natural origin, the C
6-C
22 fatty alcohols that react with the phosphorous pentoxide (P
2O
5) may contain a great variety of alkyl and/or alkenyl groups, said groups being linear
or branched, saturated or unsaturated.
[0018] Particularly preferred are C
6-C
22 fatty alcohols are derived from coconut oil, palm oil and olive oil. It is particularly
preferred that the C
6-C
22 fatty alcohols to be reacted with the phosphoric acid esters are derived from olive
oil.
[0019] The phosphoric acid esters obtained by reacting in C
6-C
22 fatty alcohols with phosphorous pentoxide (P
2O
5) are a mixture of phosphoric mono-esters (mono-alkyl esters) and phosphoric di-esters
(di-alkyl esters) and the products obtained and the reaction are well known to the
skilled person (O'Lenick et al., Soap Cosmetics and Chemical Specialities, July 1986,
p. 26.)
[0020] According to the invention it is preferred that the weight ratio phosphoric mono-esters
to phosphoric di-esters is from 50:50 to 95:5, more preferred from 55:45 to 90:10.
[0021] According to the invention in the phosphoric acid esters of formula (I) Z represents
hydrogen or an appropriate cation, said cation preferably being selected from the
group consisting of an alkali metal, an alkaline earth metal, ammonium, an alkylammonium,
an alkanolammonium or a glucammonium. It is further preferred that Z represents hydrogen
or an alkali metal, preferably lithium, sodium or potassium.
[0022] According to the invention, it is also preferred that the C
16-C
18 proportion in the alkyl and/or alkenyl groups of the phosphoric acid esters is higher
than 70%, preferably higher than 80%, even more preferably higher than 85%.
[0023] Optionally, the C
6-C
22 fatty alcohols are ethoxylated, having an average ethoxylation degree from 1 to 10,
preferably from 2 to 8.
[0024] Examples of commercially available phosphoric acid esters are FOSFODET
® 20 M (potassium salt of phosphoric ester of lauric alcohol, mono-ester to di-ester
ratio 80:20); FOSFODET
® 20 D (potassium salt of phosphoric ester of lauric alcohol, mono-ester to di-ester
ratio 50:50), FOSFODET
® 8050 (phosphoric ester of hydrogenated tallow, mono-ester to di-ester ratio 60:40),
FOSFODET
® FJZ 903 (phosphoric ester of ethoxylated (3 EO) oleyl alcohol, mono-ester to di-ester
ratio 55:45), all marketed by KAO Chemicals Europe.
The ether carboxylates
[0026] The process is divided into two steps. The first one is the alkoxylation of alcohols
under standard conditions known by the skilled in the art. For instance, the polyoxyethylene
group is obtained by addition of ethylene oxide to fatty alcohols, mostly with an
alkaline catalyst such as NaOH, KOH or NaOCH
3, giving a broad polyoxyethylene oxide distribution (broad ethoxylation degree). For
special applications the ethoxylation can be catalyzed by Lewis acids or by using
metallic Na or NaH to achieve a narrow range distribution (narrow ethoxylation degree).
[0027] However, one may also start from commercially available ethoxylated alcohols.
[0028] In the second step, the ethoxylated alcohols are reacted with a strong base, like
sodium or potassium hydroxide, in presence of a reducing agent, i.e. sodium borohydride,
to obtain the corresponding alkoxylate, which is carboxymethylated with sodium monochloroacetate
(SMCA).
[0029] The ether carboxylates of formula (II) are derived from C
6-C
22 fatty alcohols, which are preferably derived from natural fat and oil as well as
synthetic origin. Preferred fats and oils include palm oil, coconut oil, sunflower
oil, rapeseed oil, castor oil, olive oil, soybean oil; and animal fat such as tallow,
bone oil; fish oil, hardened oils and semihardened oils thereof; and mixtures thereof.
As a result of its natural origin, the C
6-C
22 fatty alcohols that are alkoxylated and subsequently carboxymethylated may contain
a great variety of alkyl and/or alkenyl groups, said groups being linear or branched,
saturated or unsaturated.
[0030] Particularly preferred are C
6-C
22 fatty alcohols are derived from coconut oil, palm oil and olive oil. It is particularly
preferred that the C
6-C
22 fatty alcohols that are alkoxylated and subsequently carboxymethylated are derived
from olive oil.
[0031] According to the invention, it is preferred that in the ether carboxylates of formula
(II) n has a value in the range of 1 to 10, preferably in the range of 1 to 7, and
M is hydrogen, sodium or potassium.
[0032] Furthermore, it is also preferred that in the C
6-C
22 alkyl and/or alkenyl group in the ether carboxylates of formula (II) the C
16-C
18 proportion is higher than 80%, more preferred higher than 80%, even more preferred
higher than 85%.
[0033] Examples of commercially available ether carboxylates of formula (II) are AKYPO
® RO 10 VG (Oleic ether carboxylic acid with an average ethoxylation degree of 1),
AKYPO
® RO 20 VG (Oleic ether carboxylic acid with an average ethoxylation degree of 2),
AKYPO
® RO 50 VG (Oleic ether carboxylic acid with an average ethoxylation degree of 5),
and AKYPO
® RO 90 VG (Oleic ether carboxylic acid with an average ethoxylation degree of 9),
all marketed by KAO Chemicals Europe.
The fatty acids
[0034] According to the invention, the C
6-C
22 fatty acids can be selected from natural and/or synthetic origin. Accordingly, natural
fatty acids may also be used in addition to synthetic fatty acids. The natural acids
do not normally occur in pure form and are therefore preferably used for the purposes
of the invention in the form of mixtures, which may be obtained from a variety of
natural sources. Accordingly, the fatty acids are preferably selected from hexanoic
acid, heptanoic acid, octanoic acid, nonanoic acid, 9-hexadecenoic acid, 9,12-octadecadienoic
acid, 9,12,15-octadecatrienoic acid, 5,8,11,14-eicosatetraenoic acid, 4,8,12,15,19-docosapentaenoic
acid, sperm oil acid, coconut oil acid, oleic acid, tall oil acid, sunflower oil acid,
linseed oil acid, and/or rapeseed oil acid.
[0035] The C
6-C
22 fatty acids are optionally ethoxylated with 1 to 20 moles of ethylene oxide, preferably
with 1 to 10 moles of ethylene oxide.
[0036] It is preferred that the C
16-C
18 proportion in the fatty acids according to the invention is higher than 70%, preferably
higher than 80%, even more preferably higher than 85%.
The fatty alcohols
[0037] Fatty alcohols are aliphatic alcohols derived from natural fats and oils. Due to
their amphipathic nature, fatty alcohols behave as nonionic surfactants. They find
use as emulsifiers, emollients and thickeners in cosmetics and food industry.
[0038] Fatty alcohols are a common component of waxes, mostly as esters with fatty acids
but also as alcohols themselves.
[0039] Examples of C
6-C
22 fatty alcohols include capryl alcohol (1-octanol), pelargonic alcohol (1-nonanol),
capric alcohol (1-decanol), lauryl alcohol (1-dodecanol), myristyl alcohol (1-tetradecanol),
cetyl alcohol (1-hexadecanol), palmitoleyl alcohol (cis-9-hexadecan-1-ol), stearyl
alcohol (1-octadecanol), isostearyl alcohol (16-methylheptadecan-1-ol), elaidyl alcohol
(9E-octadecen-1-ol), oleyl alcohol (cis-9-octadecen-1-ol), linoleyl alcohol (9Z, 12Z-octadecadien-1-ol),
elaidolinoleyl alcohol (9E, 12E-octadecadien-1-ol), linolenyl alcohol (9Z, 12Z, 15Z-octadecatrien-1-ol),
elaidolinolenyl alcohol (9E, 12E, 15-E-octadecatrien-1-ol), ricinoleyl alcohol (12-hydroxy-9-octadecen-1-ol),
arachidyl alcohol (1-eicosanol), behenyl alcohol (1-docosanol), and erucyl alcohol
(cis-13-docosen-1-ol).
[0040] The C
6-C
22 fatty alcohols are optionally ethoxylated with 1 to 20 moles of ethylene oxide, preferably
with 1 to 10 moles of ethylene oxide.
[0041] It is preferred that the C
16-C
18 proportion in the fatty alcohols according to the invention is higher than 70%, preferably
higher than 80%, even more preferably higher than 85%.
The lubricant composition
[0042] The active matter content of the lubricant composition preferably ranges from 2 to
75% by weight, more preferably from 3 to 50% by weight, even more preferably from
4 to 25% by weight. The active matter of the lubricant composition is substantially
provided by components (a), (b), (c) and (d).
[0043] The lubricant composition can be applied directly or in the form of partially diluted
compositions. Said partially diluted compositions can be obtained by diluting a lubricant
concentrated composition as described in the International patent application
PCT/EP2007/002772 or, alternatively, can be prepared in situ, depending on its active matter content.
Dilution from a lubricant concentrated composition is preferred to avoid transport
and storage of diluted compositions.
[0044] Dilution of the lubricant concentrated composition to obtain the lubricant partially
diluted composition can be done with an appropriate inert solvent or mixture thereof.
[0045] Examples of appropriate inert solvents are mineral oils, paraffin and waxes derived
from petroleum, animal and vegetable oils (like beef tallow, lard, horse grease, yolk
oil, olive oil, lanolin, jojoba oil, rapeseed oil and soybean oil), natural waxes
(like carnauba wax), C
1-C
6 alcohols (like methanol, ethanol, n-propanol, i-propanol, n-butanol, n-pentanol or
n-hexanol), C
6-C
22 fatty alcohols as described before, C
6-C
22 fatty acids as described before, ether carboxylates as described before, water (hard
water, semi-hard water or soft water), or polyols (polyhydric alcohol having two or
more hydroxyl groups in its molecule) like ethylene glycol, 1,2-propylene glycol,
1,3-propylene glycol, 1,3-butylene glycol, 1,4-butylene glycol, dipropylene glycol,
polyethylene glycol with a weight average molecular weight in the range from 100 to
1000, glycerol, alkoxylated (preferably ethoxylated) glycerol, polyglycerol, and mixtures
thereof.
[0046] According to the invention it is preferred that in the lubricant composition the
weight ratio of component (a) (phosphoric acid esters) to component (b) (ether carboxylates)
is in the range of 9:1 to 1:6, preferably in the range of 5:1 to 1:5, more preferably
in the range of 3:1 to 1:3.
[0047] According to the invention it is preferred that in the lubricant composition the
ether carboxylates of formula (II) are a mixture of
I) C6-C10 alkyl and/or alkenyl ether carboxylates having an average ethoxylation degree from
2 to 8
II) C12-C18 alkyl and/or alkenyl ether carboxylates having an average ethoxylation degree from
1 to 10, preferably from 1 to 7.
[0048] Preferably, the weight ratio of the C
12-C
18 alkyl and/or alkenyl ether carboxylates to the C
6-C
10 alkyl and/or alkenyl ether carboxylates in the lubricant composition is in the range
of 10:1 to 1:5, preferably in the range of 8:1 to 1:3.
[0049] The subject matter of the present invention also refers to a method for lubricating
conveyor systems consisting of applying, continuously or at intervals, a lubricant
composition comprising the following essential elements, expressed as weight percentage,
- a) 0.1-85% of the phosphoric acid esters of formula (I)
- b) 0.1-60% of the ether carboxylates of formula (II)
- c) 0.1-30% of the fatty acids
- d) 0.1-30% of the fatty alcohols
- e) up to 100% of an inert solvent or mixture thereof,
wherein the active matter concentration of the lubricant composition ranges from 1
to 99% by weight, preferably from 2 to 75% by weight.
[0050] The subject matter of the present invention also refers to a method for lubricating
conveyor systems consisting of applying, continuously or at intervals, a lubricant
composition comprising the following essential elements, expressed as weight percentage,
- a) 0.1-25%, preferably 0.5-15% of the phosphoric acid esters of formula (I)
- b) 0.1-20%, preferably 0.5-15% of the ether carboxylates of formula (II)
- c) 0.1-10%, preferably 0.3-5% of the fatty acids
- d) 0.1-10%, preferably 0.3-5% of the fatty alcohols
- e) up to 100% of an inert solvent or mixture thereof,
wherein the active matter concentration of the lubricant composition ranges from 3
to 50% by weight, even more preferably from 4 to 25% by weight.
[0051] The subject matter of the present invention also refers to a method for lubricating
conveyor systems consisting of applying, continuously or at intervals, a lubricant
composition comprising the following essential elements, expressed as weight percentage,
a) 0.1-25%, preferably 0.5-15% of the phosphoric acid esters of formula (I)
b1) 0.1-15%, preferably 0.5-10% of one or more of the C6-C10 alkyl and/or alkenyl ether carboxylates having an average ethoxylation degree from
2 to 8,
b2) 0.1-15%, preferably 0.5-10% of one or more of the C12-C18 alkyl and/or alkenyl ether carboxylates having an average ethoxylation degree from
1 to 10,
c) 0.1-10%, preferably 0.3-5% of one or more of the C6-C22 fatty acids,
d) 0.1-10%, preferably 0.3-5% of one or more of the C6-C22 fatty alcohols,
e) up to 100% of an inert solvent or mixture thereof,
wherein the active matter concentration of the lubricant composition ranges from 3
to 50% by weight, even more preferably from 4 to 25% by weight.
[0052] The lubricant composition can be applied to the conveyor systems continuously or
at intervals (intermittently). According to the invention, intermittent application
of the lubricant composition is preferred because of the reduced lubricant usage.
The ratio to application time to non-application time may be from 3:1 to 1:500, depending
if the lubricant composition maintains an appropriate coefficient of friction in between
lubricant applications. Specifically, the lubricant composition may be applied for
a period of time and then not applied for at least 15 minutes, at least 30 minutes,
or at least 45 minutes or longer. The application period may be long enough to spread
the composition over the conveyor belt (i.e. one revolution of the conveyor belt).
[0053] The lubricant composition is preferably applied to the conveyor surface at a location
that is not populated by packages or containers. For example, it is preferable to
apply the lubricant spray upstream of the package or container flow or on the inverted
conveyor surface moving underneath and upstream of the container or package.
[0054] Application of the lubricant composition can be carried out using any suitable technique
including spraying, wiping, brushing, drip coating, roll coating, and other methods
for application of a thin film.
[0055] The subject matter of the present invention also includes the use of the lubricant
composition defined above for lubricating conveyor systems.
[0056] A variety of kinds of conveyors systems and conveyor parts can be lubricated with
the lubricant composition. Parts of the conveyor that support or guide or move the
containers and thus are preferably coated with the lubricant composition include belts,
chains, gates, chutes, sensors, and ramps having surfaces made of fabrics, metals,
plastics, composites, or combinations of these materials.
[0057] The conveyor systems, which can be lubricated by the process according to the invention,
can be systems for a variety of materials including glasses; plastics (e.g., polyolefins
such as polyethylene and polypropylene; polystyrenes; polyesters such as polyethylene
terephtalate (PET) and polyethylene naphthalate (PEN); polyamides, polycarbonates
(PC); and mixtures or copolymers thereof); metals (e.g., aluminum, tin or steel);
papers (e.g., untreated, treated, waxed or other coated papers); cartons (like the
commercially available Tetra Pack
® or SIG Combibloc
® containers); (ceramics; and laminates or composites of two or more of these materials
(e.g., laminates of PET, PEN or mixtures thereof with another plastic material). The
containers can have a variety of sizes and forms, including cartons (e.g., waxed cartons,
Tetra Pack
® or SIG Combibloc
® containers), cans, bottles, drums and the like. Preferably, the systems are suitable
for glass bottles, plastic bottles such as polyethylene terephtalate (PET) or polycarbonate
(PC) bottles, cans, glass containers and cartons containers (i.e. Tetra Pack
® or SIG Combibloc
® containers) and similar items. Said conveyor systems can particularly be found in
the foodstuff industry.
[0058] The lubricant composition can also contain additives such as ionic surfactants, non
ionic surfactants, amphoteric surfactants, foam inhibitor agents, foam regulators,
foam stabilizers, complexing agents, chelating agents, solubilizers, emulsifiers,
biocides, bactericides, disinfectants, fungicides, antioxidants, corrosion inhibitors
and pH regulators.
[0059] The pH of the lubricant composition is preferably between 2.0 and 7.0, more preferably
between 4.0 and 6.0.
[0060] The viscosity of the lubricant composition ranges from 50 to 20,000 mPa·s at 20°C,
more preferably from 100 to 10,000 mPa·s at 20°C.
[0061] As solubilizing agents, the lubricant partially diluted composition may contain solubilizing
agents that can be mixed with water or that are water-soluble. Preferably, the following
solubilizers are used:
- urea;
- C1-C6 alcohols, like methanol, ethanol, n-propanol, i-propanol, n-butanol;
- ethylene glycol and/or butyl diglycol;
- propylene glycol;
- polyethylene glycol;
- lower and higher molecular weight polyethyleneglycols [HO-(CH2-CH2-O)n-H] such as PEG-150, PEG-300, PEG-500, PEG-2000, PEG-3500 or PEG-8000;
- methoxy polyethylene glycols [CH3O-(CH2-CH2-O)n-H] having an average molecular weight ranging from 150 to 5000, such as MPEG-350,
MPEG-500, MPEG-750, MPEG-1000, MPEG-2000, MPEG-3000 or MPEG-5000;
- vegetable oils,
- mixtures of alkoxylated glycerides derived from carboxylic acids containing between
6 and 22 carbons and alkoxylated glycerin, as described in the European patent applications
EP-A-0579887, EP-A-0586323, and EP-A-1045021, and those commercially available under the trademark LEVENOL ® and marketed by KAO Chemicals Europe like Glycereth-2 Cocoate; Glycereth-7 Cocoate
and Glycereth-17 Cocoate;
- ethoxylated rapeseed fatty acid amide, preferably Polyoxyethylene (4) Rapeseedamide;
- alkoxylated, preferably ethoxylated glycerol with 1 to 30 moles of ethylene oxide,
like Glycereth-6, Glycereth-7 or Glycereth-26;
- products of the addition of 1 to 30 moles of ethylene oxide and/or 0 to 5 moles of
propylene oxide onto linear C6-C22 fatty alcohols, C12-C22 fatty acids and alkyl phenols containing 8 to 15 carbon atoms in the alkyl group
and alkylamines containing 8 to 22 carbon atoms in the alkyl group;
- alkyl and/or alkenyl oligoglycosides containing 8 to 22 carbon atoms in the alkyl
group and ethoxylated analogs thereof;
- addition products of 1 to 15 moles of ethylene oxide with castor oil and/or hydrogenated
castor oil;
- addition products of 15 to 60 moles of ethylene oxide with castor oil and/or hydrogenated
castor oil;
- partial esters of glycerol and/or sorbitan with unsaturated, linear or saturated,
branched fatty acids containing 12 to 22 carbon atoms and/or hydroxycarboxylic acids
containing 3 to 18 carbon atoms and addition products thereof with 1 to 30 moles of
ethylene oxide like, PEG 18 Glyceryl Oleate / Cocoate;
- partial esters of polyglycerol (average degree of self-condensation 2 to 8), polyethylene
glycol (weight average molecular weight 400 to 5000), trimethylolpropane, pentaerythritol,
sugar alcohols (for example sorbitol), alkyl glucosides (for example methyl glucoside,
butyl glucoside, lauryl glucoside) and polyglucosides (for example cellulose) with
saturated and/or unsaturated, linear or branched fatty acids containing 12 to 22 carbon
atoms and/or hydroxycarboxylic acids containing 3 to 18 carbon atoms and addition
products thereof with 1 to 30 moles of ethylene oxide;
- mixed esters of pentaerythritol, fatty acids, citric acid and fatty alcohol and/or
mixed esters of fatty acids containing 6 to 22 carbon atoms, methyl glucose and polyols,
preferably glycerol or polyglycerol;
in an amount corresponding to between 10 and 40% by weight of one or several of these
solubilizing agents, relative to 100 parts by weight of the total amount of the compounds
a), b) c) and d). These solubilizing agents are appropriate, in the context of the
present invention, provided that they do not reduce the lubricant effect of the lubricant
partially diluted composition.
[0063] The following examples are given in order to provide a person skilled in the art
with a sufficiently clear and complete explanation of the present invention, but should
not be considered as limiting of the essential aspects of its subject, as set out
in the preceding portions of this description.
Examples
Example 1. Lubricant partially diluted compositions
[0064] The lubricant partially diluted compositions of Table 2 were prepared. The lubricant
concentrated composition, which is diluted to obtain the lubricant partially diluted
compositions of Table 2 is described in Table 1. The values are referred to weight
percentage.
Table 1. - Lubricant concentrated composition (components as active matter)
| |
Amount |
| Polyoxyethylene (3) oleyl phosphate ester1 |
29.5 |
| Polyoxyethylene (2) oleyl ether carboxylic acid2 |
27.6 |
| Polyoxyethylene (5) oleyl ether carboxylic acid3 |
3.4 |
| Polyoxyethylene (8) capryl ether carboxylic acid4 |
16.7 |
| Oleic Acid |
12.1 |
| Oleyl alcohol |
7.3 |
| Deionized water |
3.4 |
1Phosphoric ester of ethoxylated (3 EO) oleyl alcohol, mono-ester to di-ester ratio
55:45
2Oleic ether carboxylic acid with an average ethoxylation degree of 2
3Oleic ether carboxylic acid with an average ethoxylation degree of 5
4Caprylic ether carboxylic acid with an average ethoxylation degree of 8 |
Table 2. - Lubricant partially diluted compositions (components as active matter)
| |
Composition |
Concentration |
| 1 |
Concentrated composition of Table 1 |
10 wt.% dilution in water* |
| 2 |
Concentrated composition of Table 1 |
10 wt.% dilution in oleyl alcohol |
| 3 |
Concentrated composition of Table 1 |
10 wt.% dilution in mineral oil |
| * tap water from Emmerich am Rhein (Germany), specifically of hardness 17°dH (German
degrees) according to the regulation UNE-EN 12829 |
Example 2. Lubrication in conveyor systems
[0065] Tests to measure friction resistance were performed for glass bottles, PET bottles
and drinking cans on a stainless steel conveyor belt under the following conditions:
- Speed of bottles/drinking cans: approximately 0.5 m/s.
- Continuous/discontinuous spraying of the conveyor belt with a lubricant composition
as indicated in Table 3.
- Spraying concentration of the nozzle: approximately 15 g/hour.
- For glass bottles: measurement of the resistance of 7 beer bottles type Ale 0.5 L,
filled with water, as a tensile force using a dynamometer. These bottles are arranged
in a plastic crate for beer that permits their rotation on the belt but prevents them
from toppling over.
- For PET bottles: measurement of the resistance of 6 PET bottles type "weiße Brunnen-Einheitsflaschen
0.5 L" (Rostiprimpac), filled with water, as a tensile force using a dynamometer.
These bottles are arranged in a steel frame for the PET bottles that permits their
rotation on the belt but prevents them from toppling over.
- For drinking cans: measurement of resistance of 5 Coca-Cola drinking cans 0.33 L,
original filled, as a tensile force using a dynamometer. These drinking cans are arranged
in a plastic frame for drinking cans that permits their rotation on the belt but prevents
them from toppling over.
[0066] The dynamic friction coefficient (µ) is defined as the coefficient between the tensile
force measured for a bottle or drinking can and the weight of this bottle or drinking
can expressed in grams. This coefficient is determined when a constant value is obtained.
[0067] Foam production is controlled visually. The compositions according to the invention
present no foam formation or slightly foam formation.
[0068] Table 3 shows the friction coefficients obtained for the lubricant compositions described
in Table 2 of Example 1 as well as for comparative experiment (C1)
Table 3. - Friction coefficients (µ)
| |
Friction coefficients (µ) |
|
| Lubricant composition |
Glass bottles |
PET bottles |
Drinking cans |
Spraying |
| 1 |
0.11 |
0.08 |
0.13 |
Continuous dosage over 60 min |
| 2 |
0.11 |
0.08 |
0.11 |
Continuous dosage over 60 min |
| 0.11 |
0.08 |
0.11 |
After 30 min drying time without further dosage |
| 3 |
0.13 |
0.10 |
0.12 |
Continuous dosage over 60 min |
| 0.13 |
0.10 |
0.11 |
After 30 min drying time without further dosage |
| C1* |
0.38 |
0.13 |
0.30 |
Continuous dosage over 60 min |
| * Dry lubricant commercially available (Teflon in mineral oil) |
[0069] From the experimental results it can be shown that the method according to the invention
permit to reduce the friction over the conveyor system (lower friction coefficients)
in comparison with the comparative experiment for glass bottles, PET bottles and drinking
cans. Thus, more versatile lubricant compositions for conveyor systems can be obtained.
[0070] Additionally, the friction coefficient obtained with the lubricant partially diluted
compositions 2-5 was maintained stable for 30 minutes after said compositions were
applied to the conveyor belt for the different type of recipients (glass bottles,
PET bottles and drinking cans)
1. Method for lubricating conveyor systems consisting of applying, continuously or at
intervals, a lubricant composition comprising the following essential elements, expressed
as weight percentage,
a) one or more phosphoric acid esters of formula (I)

wherein
- R1 represents a linear or branched, saturated or unsaturated C6-C22 alkyl and/or alkenyl group, or a R3(OCH2CH2)m group;
- R2 represents hydrogen, a linear or branched, saturated or unsaturated C6-C22 alkyl and/or alkenyl group, or a R3(OCH2CH2)m group ;
- R3 represents hydrogen or a linear or branched, saturated or unsaturated C6-C22 alkyl and/or alkenyl group;
- m represents a number of from 1 to 15; and
- Z represents hydrogen or an appropriate cation
b) one or more ether carboxylates of formula (II)
R-O- (CH2CH2O)n-CH2COOM (II)
wherein
- R represents a linear or branched, saturated or unsaturated C6-C22 alkyl and/or alkenyl group;
- n represents a number of from 0.5 to 20, and
- M represents hydrogen or an appropriate cation, selected from the group consisting
of an alkali metal, an alkaline earth metal, ammonium, an alkylammonium, an alkanolammonium
or a glucammonium;
c) one or more C6-C22 fatty acids, optionally ethoxylated with 1 to 20 moles of ethylene oxide;
d) one or more C6-C22 fatty alcohols, optionally ethoxylated with 1 to 20 moles of ethylene oxide,
e) an inert solvent or mixture thereof,
wherein the active matter concentration of said lubricant composition ranges from
1 to 99% by weight.
2. Method according to claim 1, wherein the active matter concentration of the lubricant
composition ranges from 2 to 75% by weight, preferably from 3 to 50% by weight.
3. Method according to claim 1 or 2, wherein the phosphoric acid esters of formula (I)
comprise a mixture of mono- and di-esters.
4. Method according to any of the preceding claims, wherein the phosphoric acid esters
of formula (I) are ethoxylated having an average ethoxylation degree from 2 to 8.
5. Method according to any of the preceding claims, wherein in the ether carboxylates
of formula (II) n has a value in the range of 1 to 10 and M is hydrogen, sodium or
potassium.
6. Method according to any of the preceding claims, comprising, wherein the lubricant
composition comprises the following essential elements, expressed as weight percentage,
a) 0.1-85% of the phosphoric acid esters of formula (I)
b) 0.1-60% of the ether carboxylates of formula (II)
c) 0.1-30% of the fatty acids
d) 0.1-30% of the fatty alcohols
e) up to 100% of an inert solvent or mixture thereof,
wherein the active matter concentration of the lubricant composition ranges from 1
to 99% by weight.
7. Method according to any of the preceding claims, wherein the ether carboxylates of
formula (II) are a mixture of
I) C6-C10 alkyl and/or alkenyl ether carboxylates having an average ethoxylation degree from
2 to 8
II) C12-C18 alkyl and/or alkenyl ether carboxylates having an average ethoxylation degree from
1 to 10.
8. Method according to claim 7, wherein the weight ratio of the C12-C18 alkyl and/or alkenyl ether carboxylates to the C6-C10 alkyl and/or alkenyl ether carboxylates is in the range of 10:1 to 1:5.
9. Method according to any of the preceding claims wherein the conveyor system is for
glass bottles, plastic bottles such as polyethylene terephtalate (PET) or polycarbonate
(PC) bottles, cans, glass containers, drums, cardboard containers and similar items.
10. Use of a lubricant composition according to any one of the preceding claims for lubricating
conveyor systems.
11. Use according to claim 10 wherein the conveyor system is for glass bottles, plastic
bottles such as polyethylene terephtalate (PET) or polycarbonate (PC) bottles, cans,
glass containers, drums, cardboard containers and similar items.