FIELD OF THE INVENTION
[0001] The present invention relates to grease compositions, methods for manufacturing the
grease compositions, and the use of the grease compositions for lubricating bearings,
gears and couplings.
BACKGROUND OF THE INVENTION
[0002] Grease compositions are widely used for lubricating bearings and other structural
components. A grease is an essential product to reduce, for example, wear, friction,
running temperatures and energy losses. Greases are materials which comprise a base
oil that is thickened with a metal soap, and they are usually prepared by reacting
a metal hydroxide with a fatty acid in the presence of the base oil. Conventional
metal soap greases require an energy intensive grease cooking and milling process
in order to achieve proper thermo-mechanical stability. Conventional metal soap greases
can still be sensitive to poor thermo-mechanical stability and can require additional
treatments. It is known to improve further the stability, and thus the lubricating
capacity, of conventional greases by adding solid additives during the thickening
process. Examples of such solid additives are, for example, molybdenum disulfide,
graphite, zinc oxide and/or a silica gel. The process of grease cooking and milling
and additional treatments is relatively expensive because it is carried out at an
elevated temperature and over a relatively long period of time. Moreover, the greases
so prepared are still unsuitable for a variety of applications, and not all conventional
greases are suitable for food and beverage processing applications.
[0003] In
WO 2011/015337 A2, a non-hydroxide grease composition is described comprising a base oil and a thickener
which comprises amorphous hydrophilic silicon oxide particles and one or more metal
salts of different organic acids.
US 8,455,415 discloses a grease composition including a base oil, a metal soap thickener formed
from for instance lithium and fatty acid ester, and nanoparticles formed from SiC
or diamond and having an average primary particle size of 5 nm or smaller.
[0004] Consequently, there is a need for greases which can easily be manufactured at low
costs, which are stable and show highly attractive lubricating properties in terms
of low friction performance. In addition, there is a need for greases that are biodegradable,
environmentally benign and food compatible.
SUMMARY OF THE INVENTION
[0005] Object of the present invention is to provide grease compositions which show excellent
lubricating properties such as grease life performance, corrosion wear and thermo
and mechanical stability, and which can easily be manufactured at low costs and/or
are more environmental friendly.
[0006] Surprisingly, it has now been found that this can be established when use is made
of a base oil and a thickener which comprises amorphous hydrophilic fumed silicon
oxide particles and a particular ester.
[0007] Accordingly, the present invention relates to a grease composition as defined in
claim 1.
[0008] The present invention in addition relates to a grease composition comprising a base
oil and a thickener which comprises amorphous hydrophilic fumed silicon oxide particles
and one or more esters that contain one or more unsaturated C-C bonds and at least
one OH group, wherein the amorphous hydrophilic fumed silicon oxide particles have
a BET specific surface area of at least 10 m
2/g and at least 80% of the amorphous hydrophilic fumed silicon oxide particles have
a particle size in the range of from 5 nm to 50 nm, and wherein the amount of the
thickener is in the range of from 0.1-40% by weight, based on the total weight of
the grease composition.
[0009] Suitably, the thickener comprises in addition one or more metal salts such as metal
sulphonates, metal sulphates, metal phosphates and/or metal phosphonates.
[0010] The grease compositions according to the present invention show an attractive low
friction performance, whereas at the same time they can easily be manufactured at
low costs and/or are more environmental friendly.
DETAILED DESCRIPTION OF THE INVENTION
[0011] The thickener to be used in the present grease composition comprises one or more
esters that contain at least one OH group. Preferably, the one or more esters contain
one or more unsaturated C-C bonds and at least one OH group.
[0012] Esters are derived from an acid in which one OH group has been replaced by an alkoxy
group (-O-). Often esters are derived from a carboxylic acid and an alcohol. Esterification
is the chemical reaction of the acid and the alcohol to form the ester and is usually
in the presence of a catalyst, a dehydrating agent.
[0013] Suitably, the one or more esters are diesters. Suitably, the one or more esters contain
two or more unsaturated C-C bonds. Suitably, the one or more esters contain at least
two OH groups. Suitably, the one or more esters contain at least two unsaturated C-C
bonds and at least one OH group. Preferably, the one or more esters contain at least
two unsaturated C-C bonds and at least two OH groups. Suitably, the one or more esters
are metal salts. Suitably, the one or more esters comprise glycerol esters, such as
for example triglycerol esters.
[0014] Suitably, the one or more esters are esterified fatty acids that contain at least
one OH group. It will be understood that fatty acids are aliphatic monocarboxylic
acids derived from, or contained in esterified form in an animal or vegetable fat,
oil or wax. In accordance with the present invention use can be made of natural and
synthetic fatty acids. Suitable fatty acids from which the esterified fatty acids
can be made include caprylic acid, pelargonic acid, capric acid, lauric acid, linderic
acid, rayristic acid, tsuzuic acid, physetoleic acid, myristoleic acid, pentadecylic
acid, palmitic acid, palmitoleic acid, margaric acid, stearic acid, 12-hydroxystearic
acid, petroselinic acid, oleic acid, elaidic acid, vaccenic acid, linolic acid, linolenic
acid, elaeostearic acid, tuberculostearic acid, arachidic acid, eicosadienic acid,
eicosatrienic acid, arachidonic acid, behenic acid, lignoceric acid, nervonic acid,
hexadocosanic acid, octadocosanic acid and erucic acid.
[0015] Suitably, use can be made of a mixture of different esterified fatty acids. Suitable
examples of such esterified fatty acids are for example alkyl oleate esters and alkyl
linoleate esters such as methyl oleate ester,ethyl oleate ester and ethyl linoleate
ester The grease compositions may also contain a double esterified fatty ester in
which two ester groups are present. Suitable examples of such diesters are for instance
dioctylsebacic ester, dioctylsebacate ester and diisooctyl sebacate ester. Suitably,
the one or more (di)esters contain two or more unsaturated C-C bonds. In addition,
the (di)esters contain at least one OH group. Suitable examples of such esters include
such methyl-12-hydroxystearate ester, 9-Octadecenoic acid, 12 hydroxy methyl ester
and hydroxy palmitic ester.
[0016] The one or more esters to be used in accordance with the present invention have a
relative polarity which is introduced by means of an OH-group on for example a secondary
position in the fatty acid chain. In this way an improved low friction performance
could be realized.
[0017] The esters to be used in accordance with the present invention include branched and
unbranched esters. The esters may contain an amine group and/or amide group.
[0018] Suitably, the thickener comprises in addition one or more metal salts such as metal
sulphonates, metal sulphates, metal phosphates and/or metal phosphonates. When the
one or more esters are metal salts, the amount of metal (salt(s) is in the range of
from 0.1-40% by weight, based on the total weight of the grease composition. When
one or more esterfified fatty acids are metal salts, the amount of metal salt(s) is
in the range of from 0.1-40% by weight, based on the total weight of the grease composition.
The metal in the metal salts is preferably an alkali metal or an alkaline earth metal
of Groups 1 and 2 of the Periodic System of Elements, and bismuth. Suitable examples
of metals include lithium, potassium, sodium, calcium, aluminium, rubidium, cesium,
francium, beryllium, strontium, barium, radium, bismuth and magnesium. In addition
it is noted that the metal in the metal salt to be used can be a semi-metal such as
borium. According to a preferred embodiment according to the present invention, the
metal is an alkaline earth metal, most preferably calcium.
[0019] Suitably, the thickener comprises in addition one or more metal salts such as metal
sulphonates, metal sulphates, metal phosphates and/or metal phosphonates.
[0020] The grease compositions according to the present invention are non-hydroxide grease
compositions. Non-hydroxide grease compositions in accordance with the present invention
do not contain impurities such as excess amounts of hydroxide which are normally present
in greases that are prepared in conventional lime soap manufacturing processes. The
non-hydroxide grease compositions according to the present invention are suitably
substantially free of free hydroxide ions and/or metal hydroxide. Preferably, the
present non-hydroxide grease compositions contain less than 0.2% by weight, and more
preferably less than 0.1% by weight of free hydroxide ions and/or metal hydroxide,
based on the total weight of the grease composition. Preferably, the present non-hydroxide
grease compositions are substantially free of free hydroxide ions and/or metal hydroxide.
Preferably, the present grease compositions contain less than 0.2% by weight, and
more preferably less than 0.1% by weight of metal hydroxide, based on the total weight
of the grease composition. Most preferably, the present non-hydroxide grease compositions
are completely free of metal hydroxide. It will be understood that OH-groups present
on the amorphous hydrophilic fumed silicon oxide particles or in an fatty acid such
as 12-hydroxy stearate or the metal salt of such an fatty acid are not to be considered
free hydroxide ions since they are bonded to silicon atoms or to a carbon atom of
the fatty acid. The thickener to be used in accordance with the present invention
is suitably a non-saponified thickener.
[0021] Examples of esters containing unsaturated C-C bonds include 1,2-dilinoleoyl-3-oleoyl-racglycerol,
glyceryl-trilinoleate, glyceryl monostearate, palmitoleic acid ethyl ester, glyceryl
trioleate, ethyl oleate, methyl oleate, methyl linoleate, methyl linolenoate, oleyl
oleate, propyl oleate, myristyl oleate, ethyl palmitoleate, ethyl linoleate, oleyl
stearate, oleyl myristate, oleyl erucate, methykl erucate, ethyl erucate and linolein.
[0022] Examples of esters containing an OH group include glyceryl-1,2-dioloate-3-palmitate,
glyceryl behenate, glyceryl adipate, glyceryl myristate, glyceryl stearate citrate,
glyceryl caprylate, glyceryl laurate, glyceryl arachidate, glyceryl palmitate, glyceryl
hydroxystearate, glyceryl stearate, Methyl 12-hydroxyoctadecanoate and hydroxyl palmitic
ester.
[0023] Examples of esters containing an OH group and an unsaturated C-C bond include glyceryl
ricinoleate ester, glyceryl linoleate, glyceryl linolenate, glyceryl palmitoleate,
glycerol dioleate, glyceryl erucate, glyceryl oleate, triethanolamine oleate, ethyl
ricinoleate, methyl ricinoleate, O-acetylricinoleic acid methyl ester and ricinolein.
[0024] Examples of diesters include diisooctylsebacid acid ester, dioctyladipate acid ester,
dioctylsebacate ester, dimethylsebacate ester and diethylsebacate ester.
[0025] The present grease composition may also comprise one or more amides.
Suitably, the amides to be used in accordance with the present invention contain one
or more unsaturated C-C bonds and/or at least one OH group. Suitably, the amides to
be used in accordance with the present invention contain one or more unsaturated C-C
bonds and at least one OH group. Suitably, the amides contain two or more unsaturated
C-C bonds. Suitably, the amides contain two or more unsaturated C-C bonds and at least
one OH group, preferably at least two OH groups.
[0026] Suitable amides that contain one or more unsaturated C-C bonds include unsaturated
amides such as oleamide and linoleamide; diamides such as ethylene bis stearamide,
hydroxy ethyl ethylene bis oleamide, ethylene bis-12-hydroxystearamide and bishydroxethyl
oleylamine; and OH-group containing amides such as hydroxy ethyl ethylene bis oleamide,
ethylene bis-12-hydroxystearamide.
[0027] Preferably, the unsaturated amides are unsaturated fatty acid amides, more preferably
the amides are metal salts of unsaturated fatty acid amides. The amides to be used
in accordance with the present invention include branched and unbranched amides. The
amides may contain an ester group.
[0028] The present invention preferably provides a grease composition comprising a base
oil and a thickener which comprises amorphous hydrophilic fumed silicon oxide particles,
one or more metal sulphonates, metal sulphates, metal phosphates and/or metal phosphonates,
a calcium salt of 12-hydroxy stearic acid and one or more esters that contain at least
one OH group, wherein the amorphous hydrophilic fumed silicon oxide particles have
a BET specific surface area of at least 10 m
2/g and at least 80% of the amorphous hydrophilic fumed silicon oxide particles have
a mean particle size of 5 nm to 50 nm, and wherein the amount of the thickener is
0.1-40% by weight, based on the total weight of the grease.
[0029] The nature of the base oil to be used in accordance with the present invention is
not essential. The base oil may be selected from the group consisting of mineral base
oils and synthetic base oils. Mineral base oils are derived from crude oils and are
either formulated on the basis of aromatic, paraffinic and/or naphthenic base oils.
Further, a wide range of synthetic base oils is known and they include esters, poly-alpha-olefins,
polysiloxanes and the like.
[0030] The base oil to be used in accordance with the present invention may comprise a base
oil blend. Suitably, blends of mineral base oils and synthetic base oils may be used.
The base oil in this invention is one which may ordinarily be used as the base oil
of a lubricating oil or as the base oil of a grease, and there are no special restrictions.
As examples mention may be made of mineral oils, synthetic oils, animal and plant
oils, and mixtures thereof. In particular it is possible to use, singly or as mixtures,
base oils which belong to Group I, Group II, Group III, Group IV and so on of the
API (American Petroleum Institute) base oil categories. Group I base oils include,
for example, paraffinic mineral oils obtained by a suitable combination of refining
processes such as solvent refining, hydrorefining, and dewaxing in respect of lubricating
oil - o fractions obtained by atmospheric distillation of crude oil. Group II base
oils include, for example, paraffinic mineral oils obtained by a suitable combination
of refining processes such as hydrorefining and dewaxing in respect of lubricating
oil fractions obtained by atmospheric distillation of crude oil. Group II base oils
refined by hydrorefining methods such as the Gulf Company method have a total sulphur
content of less than 10 ppm and an aromatic content of not more than 5% and so are
suitable for this invention. Group III base oils and Group 11+ base oils include paraffinic
mineral oils manufactured by a high degree of hydrorefining in respect of lubricating
oil fractions obtained by atmospheric distillation of crude oil, base oils refined
by the Isodewax process which dewaxes and substitutes the wax produced by the dewaxing
process with isoparaffins, and base oils refined by the Mobil wax isomerisation process.
These too are suitable for use in this invention. Concrete examples of synthetic oils
include polyolefins, polyoxyalkylene glycols such as polyethylene glycol or polypropylene
glycol, esters such as di-2- ethylhexyl sebacate or di-2-ethylhexyl adipate, polyol
esters such as trimethylolpropane esters or pentaerythritol esters, perfluoroalkyl
ethers, silicone oils, polyphenyl ethers, and so on.
[0031] The aforementioned polyolefins include polymers of various olefins or hydrides thereof.
Any olefin may be used, and as examples mention may be made of ethylene, propylene,
butene and [alpha]-olefins with five or more carbons. In the manufacture of polyolefins,
one of the aforementioned olefins may be used singly or two or more may be used in
combination. Particularly suitable are the polyolefins called poly-[alpha]-olefins
(PAO). These are base oils of Group IV. GTL (gas to liquid) base oils synthesised
by the Fischer-Tropsch method of converting natural gas to liquid fuel have a very
low sulphur content and aromatic content compared with mineral oil base oils refined
from crude oil and have a very high paraffin constituent ratio, and so have excellent
oxidative stability, and because they also have extremely small evaporation losses,
they are suitable as base oils for this invention. As typical examples of animal and
plant oils mention may be made of castor oil and rape-seed oil. The various aforementioned
oils may be used singly or in mixtures for the base oil. The aforementioned examples
are listed singly but the invention is not limited thereby.
[0032] Preferably, the base oil or the base oil blend to be used in accordance with the
present invention has a kinematic viscosity in the range of 1 to 60 000 cSt at a temperature
of 40 °C according to DIN 51562/1. Suitable base oils include ISO VG 68, ISO VG 46,
ISO VG 32, ISO VG 22, ISO VG 15 and ISO VG 10 oils.
[0033] The silicon oxide particles to be used are derived from an amorphous hydrophilic
fumed silicon oxide. Fumed silicon oxide is an exceptionally pure form of silicon
oxide made from silica tetrachloride as a starting material, as is well known in the
art. Suitable sources for the fumed silicon oxide are Aerosil(R) which is commercially
available from Evonik Industries (formerly known as Degussa) or Cap-o-Sil(R) which
is commercially available from Cabbot Corporation.
[0034] Suitably, the amorphous hydrophilic fumed silicon oxide particles have a BET specific
surface area of at least 50 m
2/g, more preferably at least 75 m
2/g, yet even more preferably at least 100 m2/g, even yet more preferably at least
125 m
2/g and most preferably at least 150 m
2/g Although is it preferred that the BET specific surface area is as high as possible,
it will usually not be higher than 500 m
2/g Methods for determining the BET specific surface area are well known in the art.
[0035] In some embodiments of the present invention, the hydrophilic metal oxide particles
have a BET specific surface area of less than 50 m
2/g.
[0036] According to the present invention at least 80% of the amorphous hydrophilic fumed
silicon oxide particles have a particle size of 5 nm to 50 nm, , preferably of 5-40
nm, more preferably of 10-40 nm and most preferably of 20-40 nm. The total particle
size distribution of the amorphous silicon oxide particles is preferably in the range
of 1-50 nm.
[0037] The grease compositions according to the invention may additionally comprise other
thickening components, e.g. polymers or other fatty compounds that contain one or
more OH-groups and/or one or more unsaturated bonds and/or one or more ester groups
and/or one or more aromatic groups. Such thickening components can suitably be present
in an amount of less than 3% by weight, preferably less than 2% by weight, based on
the total weight of the grease composition.
[0038] The grease compositions according to the present invention may comprise other additives
to tailor its suitability to a certain use as is well known in the art. Such additives
include antiwear agents, anti-corrosion agents, rust inhibitors, friction modifiers,
anti-oxidants, VI-improvers and the like as is well known by the person skilled in
the art. As suitable examples of such additives sulphonates, sulphates, phosphates
and/or phosphonates can be mentioned. Suitable sulphonates include for instance methyl
ester sulphonate, sodium methyl ester sulphonate and calium sulphonate. Suitable sulphates
include for example calcium sulphate, sodium dodecyl sulphate and sodium lauryl sulphate.
Suitable phosphates include for instance calcium hydrogen phosphate and amine phosphate.
Suitable phosphonates include for example calcium phosphonate ester and other phosphonate
esters.
[0039] Other suitable additives include silanes, (alkylated) siloxanes, metal hydroxide
silicates, silanols, hydrosilicates, metal bonded silicon compound such as Mg
3(Si
2O
5)(OH)
2. Examples of such additives are for instance polydimethyl siloxane oil, hexomethyldisiloxane,
magnesium hydrosilicate and other phyllosilicates. As well as polymethylsilesquioxane,
hydrated (metal)silicates, amorphous silica, and sythetic silica gels, which additives
are all used to improve polymer performance. Such other additives can suitably be
present in an amount in the range of from 1-40% by weight, preferably 2-20% by weight,
based on the total weight of the grease composition. In case the grease composition
contains a high amount of such other additives, e.g. 20-40% by weight, based on total
weight of the grease composition, the grease composition will display paste-type properties.
Hence, the grease composition in accordance with the present invention also includes
pastes. The other additives may also include small amounts (less than 3% by weight,
preferably less than 2% by weight, based on the total weight of the grease composition)
of further metal salts of fatty acids, but such metal salts will not substantially
contribute to the formation of the grease thickener. In that case the grease composition
will contain more than four metal salts of different fatty acids.
[0040] The present grease compositions may in addition also contain a small amount of metal
hydroxide. Suitable metal hydroxides include potassium hydroxide, aluminium hydroxide,
calcium hydroxide, lithium hydroxide, sodium hydroxide, magnesium hydroxide barium
hydroxide and bismuth hydroxide. Other suitable additives include polypropylene, polyethylene,
urea, bentonite, and other greases such as (complex) greases and PTFE/PFPE greases.
[0041] A common disadvantage of conventional manufacturing methods is that it requires a
multiple number of hours for blending the various components, gelling and cooling
of the grease composition. At a batch scale of about 1-5 metric tons, the total cooking
(gelling) and cooling can take about four hours or more, whereas grease milling can
require two or more hours. Usually, the total manufacturing time takes about eight
hours. However, the grease compositions according to the present invention can be
prepared in a very short manufacturing process, wherein blending, gelling and cooling
is preferably performed within one hour, more preferably within half an hour period.
The mechanical treatment, preferably grease milling, in accordance with the present
invention for a 5 metric ton volume can require about two or two and a half hours.
In addition, it is observed that conventional grease manufacturing processes are carried
out at high temperatures, typically in the range of from 170-220 °C, whereas the present
grease composition can suitably be prepared at a temperature below 90 °C, including
room temperature.
[0042] The present invention also provides methods for preparing the present grease compositions.
In accordance with the present invention the components of the present grease compositions
can be mixed in any possible order of sequence. Preferably, the amorphous hydrophilic
fumed silicon oxide particles and the one or more esters that contain at least one
OH group are subjected to a mechanical treatment, a thermal treatment or to both a
mechanical treatment and a thermal treatment. Hence, (a) the amorphous hydrophilic
fumed silicon oxide particles or the one or more esters that contain at least one
OH group are subjected to a mechanical treatment and/or thermal treatment; (b) a mixture
of the amorphous hydrophilic fumed silicon oxide particles and the one or more esters
that contain at least one OH group is subjected to a mechanical treatment and/or thermal
treatment; or (c) a mixture of the base oil, the amorphous hydrophilic fumed silicon
oxide particles and the one or more esters that contain at least one OH group is subjected
to a mechanical treatment and/or thermal treatment. Preferably, the amorphous hydrophilic
fumed silicon oxide particles, the one or more esters that contain at least one OH
group, or a mixture of these components is before or after mixing with the other component(s)
subjected to a mechanical treatment, a thermal treatment or to both a mechanical treatment
and a thermal treatment.
[0043] As indicated above, the grease composition may comprise any further additives. Such
further additives can be added to one or more of the components at any stage of the
preparation process of the grease composition.
[0044] Hence, the present invention also relates to a method for manufacturing a grease
composition according to the present invention, which method comprises the following
sequential steps:
- (a) subjecting the amorphous hydrophilic fumed silicon oxide particles to a mechanical
treatment, a thermal treatment or to both a mechanical treatment and a thermal treatment;
and
- (b) mixing the amorphous hydrophilic fumed silicon oxide particles so obtained with
the base oil and one or more esters that contain at least one OH group to form a grease
composition.
[0045] In case use is made of a plurality of esters, the esters may optionally be processed
together with the amorphous hydrophilic fumed silicon oxide particles in step (a).
[0046] According to another embodiment of the present invention, the amorphous hydrophilic
fumed silicon oxide particles are first mixed with the base oil and the one or more
esters that contain at least one OH group to form a grease composition, whereafter
the grease composition so formed is subjected to the mechanical treatment, the thermal
treatment or to both the mechanical treatment and the thermal treatment.
[0047] Accordingly, the present invention also relates to a method for manufacturing a grease
according to the present invention, which method comprises the following sequential
steps: (a) mixing the amorphous hydrophilic fumed silicon oxide particles with the
base oil and one or more esters that contain at least one OH group to form a grease
composition; and (b) subjecting the grease composition so formed to a mechanical treatment,
a thermal treatment or to both a mechanical treatment and a thermal treatment. The
mechanical treatment is preferably a milling step which can be performed in any suitable
milling apparatus, e.g. a high pressure homogeniser, a colloid mill, a three-roller
mill (e.g. a three-roller mill) or a worm gear mill. Preferably, the milling apparatus
is a worm gear milling apparatus. The milling step can be performed under inert conditions,
i.e. in the absence of air or oxygen and/or in the absence of water (vapour). The
thermal treatment is preferably a heating step. The heating step preferably involves
heating at a temperature in the range of 30-120 °C, more preferably 40-110 °C and
in particular 45- 90 °C. In this heating step, the water content of the amorphous
hydrophilicfumed silicon oxide particles is reduced, preferably to a water content
of the amorphous hydrophilic fumed silicon oxide particles of less than 5% by weight,
more preferably less than 1% by weight, even more preferably less than 0.5% by weight,
yet even more preferably less than 0.25% by weight, based on the total weight of the
amorphous hydrophilic fumed silicon oxide particles. The water content of the amorphous
hydrophilic fumed silicon oxide particles is usually more than 0.01% by weight, based
on the total weight of the amoprhous hydrophilic fumed silicon oxide particles.
[0048] Most preferably, the grease composition is manufactured by optionally subjecting
the amorphous hydrophilic fumed silicon oxide particles to a thermal treatment, preferably
a heating step, to reduce the water content of the amorphous hydrophilic fumed silicon
oxide particles, followed by mixing the amorphous hydrophilic fumed silicon oxide
particles with the base oil and the one or more esters that contain at least one OH
group to form a grease composition, whereafter the grease composition so formed is
subjected to a mechanical treatment, preferably a milling step.
[0049] As disclosed above, the grease composition according to the present invention comprises
a base oil, amorphous hydrophilic fumed silicon oxide particles, and one or more esters
that contain at least one OH group, wherein the amount of the metal salts(s) is 0.1-40%
by weight, based on the total weight of the grease composition.
[0050] Suitably, the amount of the amorphous hydrophilic fumed silicon oxide particles will
be 0.1-20% by weight, preferably 1-5% by weight, based on the total weight of the
amorphous hydrophilic fumed silicon oxide particles and the esters. The skilled person
will understand how such amounts can be realised starting from the respective starting
materials.
[0051] According to the present invention, the total amount of the esters, is within a range
of 0.1-20% by weight, based on the total amount of the grease composition.
[0052] The grease composition according to the present invention can be used in many applications.
However, it is in particular useful for lubricating a bearing, preferably a rolling
element bearing, e g. a spherical roller bearing, a taper roller bearing, a cylindrical
roller bearing, a needle roller bearing, a ball bearing, and may also be used to lubricate
a sliding or plain bearing It is furthermore very useful in coupling and gearing applications.
[0053] The grease compositions according to the present invention encompass NLGI (National
Lubricating Grease Institute) grades ranging from NLGI grade 000 to NLGI grade 6.
Preferably, the grease compositions according to the present invention have a dropping
point of at least 70 °C up to about 200 °C according to ASTM D-2265.
[0054] When used in low loading gearings, the grease composition has preferably a NLGI grade
of 000 to 1. When used in high loading gearings, the grease composition has preferably
a NLGI grade of 0 to 2. When used in bearings, the grease composition has preferably
a NLGI grade of 1 to 4, more preferably a NLGI grade of 2 or 3 and most preferably
a NLGI grade of 2.
Examples
[0055] The performance of four grease compositions has been tested on tribological and friction
performance on the Ball-on-disc, the Mini Traction Machine, at Imperial College, London
UK. In each case the test procedure consists of four steps, i.e. first a grease working
step which is followed by three consecutive Stribeck step tests. Two grease samples
from each of the four grease compositions have undergone the entire test procedure.
These duplications were performed to monitor the repeatability of the test between
two different tests carried out in the exact same conditions. The same ball and disc
used for each of the grease samples were cleaned prior to running of the tests and
the test repeat. The tests were run with fresh grease.
[0056] The grease working step had the purpose of ensuring an even distribution of the grease
and to prepare the same initial condition for each test, by shearing the grease in
the same way and for the same time, before the start of the actual test.
Table 1
| |
Grease working step (1st step) |
Stribeck steps (2nd, 3rd, 4th steps) |
| Load [N] |
1 |
31 |
| Max Hertz pressure [GPa] |
0.31 |
0.96 |
| Temperature [°C] |
60 |
60 |
| Speed range [mm/s] |
5 (constant) |
5 - 1000 (in 50 log steps) |
| SRR [%] |
0 |
10 |
| Time [min] |
5 |
6 |
[0057] In Table 1, the test operating conditions during the grease working step and the
Stribeck test steps are shown.
[0058] In the four test procedure steps, the following operating conditions were applied:
Step 1 - Grease working step: a ball load of 1 N was applied on the disc resulting
in Hertzian contact pressure of 0.31 GPa, and a constant speed of 5 mm/s, for 5 minutes.
Steps 2-4 - The three consecutive Stribeck steps: a ball load of 31 N was applied
on the disc resulting in a Hertzian contact pressure of 1 GPa, and the speed increased
from 5 mms/s to 1000 mms/s at a slide-to-roll ratio (SRR) of 10 %. This step was repeated
three times to monitor the repeatability of the step within the same test, and to
analyse the friction coefficient evolution after each step due to the grease thixotropic
character.
[0059] A test sample 1 according to the present invention was manufactured from a paraffinic
mineral blend base oil of 120 cSt from Scharr, Tunap, and 10wt.% calciumhydroxystearate
from Barlocher, 2 wt.% calciumstearate from Barlocher, 3 wt.% aerosol from Evonik
i.e. hydrophilic silicon oxide primary particles having a BET specific surface area
of 175-220 m
2/g and the primary particle size ranges typically between 7-25 nm, 1.2 wt.% triphenylphosphate
from M. Volkholz, 2 wt.% disodiumsebacic acid from M. Volkholz, 0.5 wt.% alkylphosphateamine
from Ciba, 0.5 wt.% from butylated triphenyl phosphorothionate from Ciba, 0.5 wt.%
benzotriazole from Ciba, 2.5 wt.% triphenylphosphorothionate from Ciba, 2 wt.% ditertdodecylpolysulfide
from Elf Atochem, 5 wt.% dioctylsebasicacid-acid ester from Croda and 5 wt.% glyceryl
isostearate from Croda. The grease has been composed by adding, mixing and milling
in a 3-roller-mill for 30 minutes in total.
[0060] For comparison reasons, test sample 1 of the present invention was compared with
three reference greases of the following compositions:
- (a) Li-1 comprising of lithium salts as a grease thickener, and having a mineral base
oil viscosity of 100 mm2/s at 40 °C;
- (b) Li-2 comprising lithium salts as a grease thickener, and a mineral base oil viscosity
of 200 mm2/s at 40 °C;
- (c) CaSX-1 comprising calcium sulfonate and calcium salts as a grease thickener, and
a base oil blend of mineral and synthetic PAO base oil of a viscosity of 80 mm2/s at 40 °C.
[0061] In Figure 1, the results of the test sample 1 and the three reference grease compositions
are compared with each other, whereby the values of the Stribeck friction coefficient
[-] and the entrainment speed [mms
-1] measurements obtained on the MTM rig are shown. The boundary, mixed and full film
lubricating regimes are indicated in the figure over the ranges of entrainment speeds.
[0062] A test sample 2 according to the present invention has been manufactured from a paraffinic
mineral blend base oil of 120 cSt from Scharr, Tunap, and 10wt.% calciumhydroxystearate
from Barlocher, 2 wt.% calciumstearate from Barlocher, 3 wt.% aerosol from Evonik
i.e. hydrophilic silicon oxide primary particles having a BET specific surface area
of 175-220 m
2/g and the primary particle size ranges typically between 7-25 nm, 1.2 wt.% triphenylphosphate
from M. Volkholz, 2 wt.% disodiumsebacic acid from M. Volkholz, 0.5 wt.% alkylphosphateamine
from Ciba, 0.5 wt.% from butylated triphenyl phosphorothionate from Ciba, 0.5 wt.%
benzotriazole from Ciba, 2.5 wt.% triphenylphosphorothionate from Ciba, 2 wt.% ditertdodecylpolysulfide
from Elf Atochem, 10 wt.% glyceryl isostearate ester from Croda. The grease has been
composed by adding, mixing and milling in a 3-roller-mill for 30 minutes in total.
[0063] For comparison reasons, test sample 2 of the present invention was compared with
three reference greases of the following compositions:
- (a) Li-1 comprising of lithium salts as a grease thickener, and having a mineral base
oil viscosity of 100 mm2/s at 40 °C;
- (b) Li-2 comprising lithium salts as a grease thickener, and a mineral base oil viscosity
of 200 mm2/s at 40 °C;
- (c) CaSX-1 comprising calcium sulfonate and calcium salts as a grease thickener, and
a base oil blend of mineral and synthetic PAO base oil of a viscosity of 80 mm2/s at 40 °C.
[0064] In Figure 2, the results of the test sample 2 and the three reference grease compositions
are compared with each other, whereby the values of the Stribeck friction coefficient
[-] and the entrainment speed [mms
-1] measurements obtained on the MTM rig are shown. The boundary, mixed and full film
lubricating regimes are indicated in the figure over the ranges of entrainment speeds.
[0065] A test sample 3 according to the present invention has been manufactured from a paraffinic
mineral blend base oil of 120 cSt from Scharr, Tunap, and 10wt.% calciumhydroxystearate
from Barlocher, 2 wt.% calciumstearate from Barlocher, 3 wt.% aerosol from Evonik
i.e. hydrophilic silicon oxide primary particles having a BET specific surface area
of 175-220 m
2/g and the primary particle size ranges typically between 7-25 nm, 1.2 wt.% triphenylphosphate
from M. Volkholz, 2 wt.% disodiumsebacic acid from M. Volkholz, 0.5 wt.% alkylphosphateamine
from Ciba, 0.5 wt.% from butylated triphenyl phosphorothionate from Ciba, 0.5 wt.%
benzotriazole from Ciba, 2.5 wt.% triphenylphosphorothionate from Ciba, 2 wt.% ditertdodecylpolysulfide
from Elf Atochem, and 10 wt.% dioctylsebasicacid-acid ester from Croda. The grease
has been composed by adding, mixing and milling in a 3-roller-mill for 30 minutes
in total.
[0066] For comparison reasons, test sample 3 of the present invention was compared with
three reference greases of the following compositions:
- (a) Li-1 comprising of lithium salts as a grease thickener, and having a mineral base
oil viscosity of 100 mm2/s at 40 °C;
- (b) Li-2 comprising lithium salts as a grease thickener, and a mineral base oil viscosity
of 200 mm2/s at 40 °C;
- (c) CaSX-1 comprising calcium sulfonate and calcium salts as a grease thickener, and
a base oil blend of mineral and synthetic PAO base oil of a viscosity of 80 mm2/s at 40 °C.
[0067] In Figure 3, the results of the test sample 3 and the three reference grease compositions
are compared with each other, whereby the values of the Stribeck friction coefficient
[-] and the entrainment speed [mms
-1] measurements obtained on the MTM rig are shown. The boundary, mixed and full film
lubricating regimes are indicated in the figure over the ranges of entrainment speeds.
[0068] From Figures 1-3, it will be clear that that the test samples 1-3 in accordance with
the present invention constitute an improvement in terms of lubrication and friction
when compared with the three reference grease compositions.