[0001] The present invention relates to a water-soluble aluminium and aluminium alloys hot
rolling composition and to a process for hot rolling aluminium and aluminium alloys.
[0002] The aluminium and aluminium alloys rolling industry expresses the need to maximize
the efficiency of their rolled metal manufacturing process. In general terms, this
means that there is a wish to operate at higher rolling speeds and to produce more
marketable products per operating shift. Additionally, there is also a wish to minimize
the number of passes through the mill taken to achieve a given level of reduction.
Both these routes require that quality and surface finish be not compromised.
[0003] The invention thus provides an oil composition for hot rolling mills that affords
the following customer benefits:
- a higher reduction ratio : one pass reduction is in most cases achievable;
- a better rolling ability (i.e. a lower rolling force and a reduced power consumption
) as compared to the rolling ability obtained with oil compositions of the prior art;
- an improved rolled surface finish quality;
- a shorter emulsion break-in period, which is the time required to obtain the optimal
partical size distribution;
- an excellent resistance to corrosion; and
- a high lubricity (plate-out properties, roll coating).
[0004] The invention is effective on any type of hot rolling, be it reversible or not, on
breakdown, tandem and combination mills.
[0005] Especially, the invention exhibits high reduction and rolling capabilities while
providing an excellent strip surface finish when rolling at high speed.
[0006] The prior art does not teach or even suggest the instant invention.
[0007] Thus, the invention provides a water-soluble aluminium and aluminium alloys hot rolling
oil composition comprising a base stock oil and, based on the total weight of the
composition, from 1 to 80%, preferably from 3 to 30% by weight of di(2-ethylhexyl)
adipate ester.
[0008] According to one embodiment, the oil composition further comprises, based on the
total weight of the composition, from 0,05 to 20%, preferably from 0,1 to 5% by weight
of a non-ionic surfactant, such as an ethylene oxide addition polymer. An example
of such an ethylene oxide addition polymer is the ethylene oxide addition polymer
sold by the company ICI under tradename Hypermer® A60.
[0009] According to a further embodiment, the oil composition further comprises, based on
the total weight of the composition, from 1 to 30%, preferably from 5 to 20% of oleic
acid. It is actually believed that the free oleic acid provides a better surface finish
to the aluminium or aluminium alloy strip.
[0010] The invention further provides a process for preparing the oil composition.
[0011] The invention further provides an emulsion containing the oil composition and a process
for preparing this emulsion.
[0012] In addition, the invention provides the use of the oil composition of the invention
to prepare emulsions intended to be used in a aluminium or aluminium alloy hot rolling
process.
[0013] The invention also provides a process for hot rolling aluminium and aluminium alloys
sheets, comprising applying an effective amount of the emulsion of the invention.
[0014] Finally, the invention provides the use of the emulsion in a hot rolling process.
[0015] The invention is now disclosed in more details in the following specification.
[0016] Figure 1 is a graph showing the applied rolling force versus the number of passes,
first, when an emulsion of the prior art and then when an emulsion of the invention
are used.
[0017] Figure 2 is a graph showing the applied net rolling power versus the number of passes,
first, when an emulsion of the prior art and then when an emulsion of the invention
are used.
[0018] The water-soluble oil compositions of the invention are neat oil concentrates generally
intended to be diluted in water to give oil-in-water emulsions.
[0019] The base stock oil is any oil typically used in the field of hot rolling. It can
be paraffinic or naphthenic.
[0020] Paraffinic base oils are made from crude oils that have relatively high alkane contents
(high paraffin and isoparaffin contents). Typical crudes are from the Middle East,
North Sea, US mid-continent. The manufacturing process requires aromatics removal
(usually by solvent extraction) and dewaxing. Paraffinic base oils are characterized
by their good viscosity/temperature characteristics, i.e. high viscosity index, adequate
low-temperature properties and good stability. They are often referred to as solvent
neutrals, where solvent means that the base oil has been solvent-refined and neutral
means that the oil is of neutral pH. An alternative designation is high viscosity
index (HVI) base oil. They are available in full range of viscosities, from light
spindle oils to viscous brightstock.
[0021] Naphthenic base oils have a naturally low pour point, are wax-free and have excellent
solvent power. Solvent extraction and hydrotreatment can be used to reduce the polycyclic
aromatic content.
[0022] A preferred base oil is a mixture of paraffinic and naphthenic oils.
[0023] The base oil typically has a viscosity from 7 to 150 cSt at 40°C, and preferably
from 20 to 50 cSt at 40°C.
[0024] The water-soluble oil composition preferably comprises a trialkanolamine (C
2-4), preferably triethanolamine, the amount of which being such that all bindable trialkanolamine
is bound to a part only of the oleic acid. The aim of this embodiment is to ensure
that there remains free oleic acid in the oil composition.
[0025] The product of the reaction of the trialkanolamine with oleic acid acts as a surfactant.
[0026] The water-soluble oil composition may comprise classical additives, such as surfactants,
coupling agents or cosurfactants, friction reducing agents or lubricity agents, corrosion
inhibitors or anti-oxidants, extreme-pressure and anti-wear agents, bactericides and
fungicides, anti-foaming agents, anti-rust agents.
[0027] Examples of anti-foaming agents are silicone based, especially polydimethylsiloxane.
[0028] Examples of corrosion inhibitors are hindered phenols and zinc dialkyldithiophosphates
(ZDDP).
[0029] Examples of extreme-pressure and anti-wear agents are dilauryl phosphate, didodecyl
phosphite, trialkylphosphate such as tri(2-ethylhexyl)phosphate, tricresylphosphate
(TCP), zinc dialkyl(or diaryl)dithiophosphates (ZDDP), phospho-sulphurized fatty oils,
zinc dialkyldithiocarbamate), mercaptobenzothiazole, sulphurized fatty oils, sulphurized
terpenes, sulphurized oleic acid, alkyl and aryl polysulphides, sulphurized sperm
oil, sulphurized mineral oil, sulphur chloride treated fatty oils, chlornaphta xanthate,
cetyl chloride, chlorinated paraffinic oils, chlorinated paraffin wax sulphides, chlorinated
paraffin wax, and zinc dialkyl(or diaryl)dithiophosphates (ZDDP), tricresylphosphate
(TCP), trixylylphosphate (TXP), dilauryl phosphate, respectively.
[0030] Examples of corrosion inhibitors or anti-oxidants are radical scavengers such as
phenolic antioxidants (sterically hindered), aminic antioxidants, organo-copper salts,
hydroperoxides decomposers, butylated hydroxytoluene.
[0031] Examples of anti-rust agents are amine derivatives of alkenyl succinic anhydride.
[0032] Examples of friction reducing agents/lubricity agents are fatty acids (C
12-20) like lauric acid, oleic acid, palmitic acid, alkyl(C
6-10) alkylate(C
12-20) esters like di(2-ethyl-hexyl) adipate.
[0033] Further elements on base oils and additives can be found in "Chemistry And Technology
Of Lubricants", R.M. Mortier and S.T. Orszulik, VCH Publisher, Inc, 1992.
[0034] The following is an example of content of the water-soluble oil composition of the
invention (the percentages are weight percentages based on the total weight of the
composition) :
- 0.1-0.5% of trialkyl (C1-4) phenol;
- 0.5-4.0% of trialkyl (C3-10) phosphate ester;
- 5-15% of di(2-ethylhexyl) adipate ester;
- 5-15% of organic fatty acid (C12-20);
- 0.5-2% of 5-carboxy 4-hexyl 2-cyclohexen 1-octanoic acid;
- 1-3% of alkylene (C2-6)glycol;
- 0.3-1% of ethoxylated alcohols (C5-14, comprising 2-10 CH2O groups);
- 2-5% of trialkanol amine (C2-4);
- the balance being a mixture of naphthenic and paraffinic lube base oils.
[0035] The oil composition is prepared by blending the base oil and the other ingredients,
preferably under stirring or with any mixing device, whilst controlling the temperature
so that is does not exceed 50°C, and more preferably, 35°C.
[0036] An oil-in-water emulsion is prepared by diluting under stirring the oil composition
of the invention in water. It is preferred to use deionized water which may previously
have been warmed to around 35°C.
[0037] The emulsion generally comprises water and, based on the total volume of the emulsion,
from 0.5 to 30%, preferably from 1 to 15%, by volume, of the oil composition.
[0038] The aluminium alloys to which the invention applies are any aluminum alloys, including
1000, 2000, 3000, 5000, 6000, 7000 series.
[0039] The hot rolling process can be the classical process. The rolled metal temperature
is generally around 600-650°C for breakdown mills and around 400-500°C for tandem
mills.
[0040] The process is preferably carried out on a breakdown rolling mill, on a tandem rolling
mill or on a finishing rolling mill. The instant oil composition allows a significant
reduction of the number of passes. With conventional prior art oils, the number of
passes was typically 13. The oil composition of the invention allows lowering this
number to two passes, which is a significant improvement.
[0041] When the hot rolling process is carried out in a breakdown mill, the emulsion preferably
comprises, based on the total volume of the emulsion, from 2 to 4% by volume of the
oil composition.
[0042] When the hot rolling process is carried out in a finishing or tandem mill, the emulsion
preferably comprises, based on the total volume of the emulsion, from 5 to 7% by volume
of the oil composition.
[0043] The following examples illustrate the invention without limiting it. All parts and
ratios are given by weight, unless otherwise stated.
Example
[0044] A composition is prepared by mixing the ingredients of Table 1 in the order in which
they appear in this table. The temperature is be maintained at a maximum of 35°C to
ensure a complete dissolution and homogeneisation of the ingredients without impairing
the properties of the emulsion.
TABLE 1
Ingredients |
Content (wt%) |
Base oil (naphthenic, 600 SUS) |
27.00 |
Base oil (paraffinic, 9 cSt at 40°C) |
44.60 |
Di-tertiobutyl paracresol (antioxidant) |
0.20 |
Trioctylphosphate ester (extreme pressure agent) |
2.00 |
Di(2-ethylhexyl)adipate ester (lubricity agent) |
8.00 |
Oleic acid (friction reducing agent/lubricity agent) |
11.6 |
5-carboxy 4-hexyl 2-cyclohexen 1-octanoic acid (corrosion inhibitor) |
1.00 |
Diethylene glycol (coupling agent) |
2.10 |
Ethylene oxide addition polymer * |
0.50 |
Triethanol amine (buffer/cosurfactant) |
3.00 |
* : sold by ICI under the tradename Hypermer® A60 |
[0045] The characteristics of the composition of Table 1 are set out in Table 2.
TABLE 2
Oil concentrate before dilution |
Unit |
Method |
Typical characteristics |
Colour (ASTM) |
|
ISO 2049 |
L 1.0 |
Density at 15°C |
G/ml |
ASTM D 1298 |
0.8908 |
Pour point |
°C |
ISO 3016 |
-27 |
Viscosity at 40°C |
CSt |
ASTM D 445 |
32.6 |
Neutralization number |
KOH mg/g |
ASTM D 974 |
25.6 |
Saponification number |
KOH mg/g |
ASTM D 94 |
51.6 |
Total base number |
KOH mg/g |
ISO 3771 |
11.5 |
[0046] An emulsion is prepared by diluting under stirring the oil composition of Table 1
in deionized water prewarmed to 35°C. The characteristics of the obtained emulsion
are given in Table 3.
TABLE 3
Emulsion |
Method |
Typical characteristics |
Stability of the 6% (v/v) emulsion(at room temperature, for 20 hours) |
Mobil 1) |
1% cream |
pH value of fresh 5% (v/v) emulsion at 20°C |
ASTM E
70-90 |
8.3 |
1) : The emulsion stability was determined according to the following procedure. 470
ml of distilled water at room temperature or test temperature were measured into a
800-ml beaker. A 50-ml stirrer having four paddles was attached to a stirring motor
so that the paddles were positioned 25mm above the bottom of the beaker. A 50-ml dropping
funnel was positioned such that the outlet was 15mm from the beaker wall. The stirrer
was turned on and the rate adjusted to 1000 rpm. The sample was then heated up to
a temperature of 35 ± 1°C. 30 ml of the test oil were added to the dropping funnel.
The dropping rate was adjusted such that all the oil was transferred to the water
within 120 ± 20 seconds. The stirring was then continued for an additional 60 seconds
while the sample temperature was maintained at 35°±1°C. The resulting emulsion was
poured into a 500-ml graduated cylinder and allow to stand at room temperature for
20 hours. After 20 hours, the upper layer (yellow cream + oil) was read in volume
percent. |
EXPERIMENTAL TESTING
[0047] A blank is first prepared by diluting a prior art oil composition which has the composition
set out in Table 4 :
TABLE 4
Ingredients |
Content (wt%) |
Paraffinic base oil (25 cSt at 40°C) |
48.5 |
Naphthenic base oil (115 cSt at 40°C) |
13.0 |
Naphthenic base oil (8 cSt at 40°C) |
20.0 |
Ditertiobutyl paracresol |
0.2 |
Organic fatty acid (C12 to C18) |
11.6 |
Dialkylene glycol |
2.1 |
Trialkanol amine (C2 to C4) |
2.6 |
Trialkylphosphate ester (C3 to C10) |
2.0 |
[0048] Two emulsions are prepared by respectively diluting the oil compositions of the invention
and of the prior art in dionized water.
[0049] Measurements with a Sephy Zetameter show that the Zeta potential of both emulsions
is -62mV, which means that these emulsions have a high stability.
[0050] Both emulsions are evaluated on an industrial test mill. The rolling conditions were
as follows :
- mill type : 2 high
- motor output : 45 kW or 67 kW
- roll diameter : 760 mm
- roll hardness : 58-61 Rockwell C
- maximal width of metal : 685 mm
- typical width of metal : 305 mm
- maximum speed : 30 m/min
- entrance temperature (ingot) : 450°C
- ingot dimensions : 305 x 610 x 1650 mm
- final thickness : 25,4 mm
- emulsion volume : 400 l
- emulsion temperature : 50°C
- emulsion concentration : 5%
[0051] The following procedure was used with each oil in the rolling tests :
1. The AA5182 blocks were lightly scalped, degreased with methyl ethyl ketone and
heated to 454°C.
2. The mill rolls were washed in a dilute solution of sodium hydroxide to remove the
roll coating from any previous rolling and then rinsed. The rinse water was checked
for residual caustic. A profilometer was used to measure surface roughness.
3. The rolls were preheated to 77°C using quartz-tube heaters.
4. The coolant sprays were adjusted to give a flow of 200 1/min with a pressure of
6.9 . 10
4 Newton/sq. meter (10 psig) on the top spray header, and 4.1 105 Newton/sq. meter
(60 psig) on the bottom header.
5. A 100 cm (4-inch) thick block of AA5182 was given 5 rolling passes using the following
nominal pass schedule. Mill speed was 18.3 m/min. All passes were in the east to west
rolling direction. The mill gap setpoints were recorded for the first emulsion tested
and then duplicated for the remaining emulsions. These settings were 1.27 mm below
the nominal desired exit thickness on each pass.
Nominal Pass Schedule :
Pass 1 |
100 mm - 83 mm |
Pass 2 |
83 mm - 65 mm |
Pass 3 |
65 mm - 50 mm |
Pass 4 |
50 mm - 37 mm |
Pass 5 |
37 mm - 25 mm |
6. A 600 mm long piece of metal was sheared from the mid-length of the 25 mm thick
piece to be used later for anodizing. The two remaining pieces were put back into
the furnace for reheating.
7. A second block was given the same treatment as indicated in items 5 and 6. Oil
concentrate was added to the emulsion to obtain a 7% volume concentration.
8. The two pieces from each of the original blocks were then rolled after reheating
at a mill speed of 18.3 m/min using the following nominal pass schedule :
Pass 6 |
25 mm - 16 mm |
Pass 7 |
16 mm - 9.5 mm |
Pass 8 |
9.5 mm - 5 mm |
9. After the last pass, two 600 mm long pieces were hot sheared from each of the pieces
rolled. This metal was saved for later inspection in the as-rolled and anodized condition.
The distance between two marks scribed on the roll was measured on the strip surface
following the last pass for use in calculating forward slip.
10. The top work roll was then sampled via caustic extraction of a known area for
the later measurement of the aluminium deposited on it.
[0052] Figure 1 is a graph showing the applied rolling force (in tons) applied on an aluminium
alloy AA5182 versus the number of passes.
[0053] As can be seen, an improvement of 2.2% on average is achieved with the emulsion of
the invention over the emulsion of the prior art.
[0054] Figure 2 is a graph showing the applied net rolling power (total power minus bearing
losses, in kW) versus the number of passes.
[0055] An improvement of 5.0% on average is achieved with the emulsion of the invention
over the emulsion of the prior art.
[0056] A pilot anodizing line was used to anodize approximately 150 mm of the length of
the 25 mm thick and 5 mm thick pieces (see above point 6) to highlight pickup and
surface appearance. The procedure was :
1. Clean for 3 minutes using a non-etching alkaline cleaner.
2. Rinse twice.
3. Nitric acid desmut for two minutes.
4. Rinse twice.
5. Anodize in 15% sulfuric acid at 15 volts for 10 minutes.
6. Rince twice
7. Dry
[0057] The results show that the brightness and uniformity of the surface finish of an aluminim
or aluminium alloy sheet after rolling with the emulsion of the invention was similar
to the brightness obtained with the emulsion of the prior art.
[0058] A roll coating measurement was carried out as follows.
1. A plexiglass, gasketed fixture was attached and sealed to the center of the top
work roll. This fixture includes a reservoir covering an area of 20.26 square centimeters
of the roll surface.
2. Fifteen milliliters of 1N sodium hydroxide was syringed into the reservoir where
it was permitted to react with the aluminum roll coating on the roll surface for approximately
5 minutes.
3. The caustic liquor was then extracted via syringe from the reservoir and placed
into a sample bottle.
4. Two 15 ml rinses with deionized water were applied, extracted with a syringe and
added to the sample bottle.
5. Total aluminum in the sample was determined via ICP.
6. The roll coating weight was then calculated and expressed as milligrams of aluminum
per square centimeter of roll surface.
[0059] The roll coating was found to be better with the invention than with the emulsion
of the prior art.
1. Water-soluble aluminium and aluminium alloys hot rolling oil composition comprising
a base stock oil and, based on the total weight of the composition, from 1 to 80%
by weight of di(2-ethylhexyl) adipate ester.
2. Water-soluble oil composition according to claim 1, further comprising, based on the
total weight of the composition, from 0,05 to 20%, preferably from 0,1 to 5% by weight
of a non-ionic surfactant, preferably an ethylene oxide addition polymer.
3. Water-soluble oil composition according to claim 1 or 2, comprising, based on the
total weight of the composition, from 3 to 30% by weight of di(2-ethylhexyl) adipate
ester.
4. Water-soluble oil composition according to any one of claims 1 to 3, further comprising,
based on the total weight of the composition, from 1 to 30%, preferably from 5 to
20% by weight of oleic acid.
5. Water-soluble oil composition according to claim 4, further comprising, a trialkanolamine
(C2-4), preferably triethanolamine, in such an amount that all bindable trialkanolamine
is bound to a part of the oleic acid.
6. Water-soluble oil composition according to any one of claims 1 to 5, comprising, in
weight percentages based on the total weight of the composition :
- 0.1-0.5% of trialkyl (C1-4) phenol;
- 0.5-4.0% of trialkyl (C3-10) phosphate ester;
- 5-15% of di(2-ethylhexyl) adipate ester;
- 5-15% of organic fatty acid (C12-20);
- 0.5-2% of 5-carboxy 4-hexyl 2-cyclohexen 1-octanoic acid ;
- 1-3% of alkylene (C2-6) glycol;
- 0.3-1% of ethoxylated alcohols (C5-14, comprising 2-10 CH2O groups) ;
- 2-5% of trialkanol amine (C2-4);
- the balance being a mixture of naphthenic and paraffinic lube base oils.
7. Water-soluble oil composition according to any one of claims 1 to 6, in which the
base stock oil has a viscosity comprised between 7 and 150 cSt at 40°C, preferably
between 20 and 50 cSt at 40°C.
8. Oil-in-water emulsion comprising water and from 0.5 to 30%, preferably from 1 to 15%
(v/v) of the water-soluble oil composition according to any one of claims 1 to 7.
9. Process for the preparation of a water-soluble oil composition according to any one
of claims 1 to 7, comprising blending the base stock and the other ingredients under
stirring or with any mixing device.
10. Process for the preparation of an oil-in-water emulsion according to claim 8, comprising
diluting the oil composition in water under stirring.
11. Hot rolling process for rolling aluminium and aluminium alloys sheets, comprising
applying an effective amount of the emulsion according to claim 8.
12. Hot rolling process according to claim 11, wherein the hot rolling process is carried
out in a breakdown mill and the emulsion comprises, based on the total volume of the
emulsion, from 2 to 4% by volume of the water-soluble oil composition according to
any one of claims 1 to 7.
13. Hot rolling process according to claim 11, wherein the hot rolling process is carried
out in a finishing or tandem mill and the emulsion comprises, based on the total volume
of the emulsion, from 5 to 7% by volume of the water-soluble oil composition according
to any one of claims 1 to 7.
14. Use of the water-soluble oil composition according to any one of claims 1 to 7 to
prepare emulsions intended to be used in a aluminium or aluminium alloy hot rolling
process.
15. Use of the water-in-oil emulsion of claim 8 in a hot rolling process.