Patent Grant
8883306
The present invention relates to a steel filament and to a steel cord adapted for the reinforcement of elastomer products or of thermoplastic products.
The present invention also relates to a method of manufacturing such a steel filament and such a steel cord.
Steel filaments and steel cords adapted for the reinforcement of elastomer products such as tires, impact beams, hoses, flexible pipes, . . . are well known in the prior art.
Steel filaments and steel cords are made starting from steel wire rod. This steel wire rod typically has a steel composition along following lines. A carbon content of more than 0.60 per cent by weight, a manganese content ranging between 0.40 per cent and 0.70 per cent by weight, a silicon content ranging between 0.15 per cent and 0.30 per cent by weight, a maximum sulphur and a maximum phosphorus content of 0.03 per cent by weight. Other micro-alloying elements may be added. An example is chromium. The steel wire rod usually has a diameter dS of 5.5 mm or of 6.5 mm.
The wire rod is firstly cleaned by mechanical descaling and/or by chemical pickling in a H2SO4 or HCl solution in order to remove the oxides present on the surface. The wire rod is then rinsed in water and is dried. The dried wire rod is then subjected to a first series of dry drawing operations in order to reduce the diameter until a first intermediate diameter.
At this first intermediate diameter d1, e.g. at about 3.0 to 3.5 mm, the dry drawn steel wire is subjected to a first intermediate heat treatment, called patenting. Patenting means first austenitizing until a temperature of about 1000° C. followed by a transformation phase from austenite to pearlite at a temperature of about 600-650° C. The steel wire is then ready for further mechanical deformation.
Thereafter the steel wire is further dry drawn from the first intermediate diameter d1 until a second intermediate diameter d2 in a second number of diameter reduction steps. The second diameter d2 typically ranges from 1.0 mm to 2.5 mm.
At this second intermediate diameter d2, the steel wire is subjected to a second patenting treatment, i.e. austenitizing again at a temperature of about 1000° C. and thereafter quenching at a temperature of 600 to 650° C. to allow for transformation to pearlite.
If the total reduction in the first and 2nd dry drawing step is not too big a direct drawing operation can be done from wire rod till diameter d2.
After this second patenting treatment the steel wire is usually provided with a brass coating: copper is plated on the steel wire and zinc is plated on the copper. A thermo diffusion treatment is applied to form the brass coating.
The brass-coated steel wire is then subjected to a final series of cross-section reductions by means of wet drawing machines. The final product is a high-tensile steel filament with a carbon content above 0.60 per cent by weight, with a tensile strength above 2000 MPa and adapted for the reinforcement of elastomer products.
Despite its wide-spread use, the above described process has a disadvantage it that it consumes a lot of energy. More particularly, the double patenting process steps and their related austenitizing furnaces require a lot of energy. As a matter of example only, a single austenitizing furnace produces a power of 374 KWatt/Ton of produced steel cord. Indeed the furnaces and the associated quenching process represent a considerable part of the CO2 production during the manufacturing of steel filaments and steel cords adapted for the reinforcement of elastomer products. The patenting process, however, is needed and cannot be cancelled as such. This patenting process restores the metal structure of the steel wire into a state which allows for further drawing. Without this patenting process the steel wires would break frequently during further drawing and would become too brittle.
It is an object of the present invention to avoid the drawbacks of the prior art.
It is also an object of the present invention to provide a steel filament with a production process which costs less energy.
It is another object of the present invention to avoid the use of austenitizing furnaces and of other intermediate heat treatments.
According to a first aspect of the present invention, there is provided a steel filament adapted for the reinforcement of elastomer products. The steel filament has a plain carbon composition. A plain carbon composition is a steel composition where—possibly with exception for silicon and manganese—all the elements have a content of less than 0.50 per cent by weight, e.g. less than 0.20 per cent by weight, e.g. less than 0.10 per cent by weight. Silicon is present in amounts of maximum 1.0 per cent by weight, e.g. maximum 0.50 per cent by weight, e.g. 0.30 wt % or 0.15 wt %. Manganese is present in amount of maximum 2.0 per cent by weight, e.g. maximum 1.0 per cent by weight, e.g. 0.50 wt % or 0.30 wt %.
In the present invention, the carbon content ranges up to 0.20 per cent by weight, e.g. up to 0.10 per cent by weight, e.g. ranging up to 0.06 per cent by weight. The minimum carbon content can be about 0.02 per cent by weight.
The plain carbon composition has mainly a ferrite or pearlite matrix and is mainly single phase. There are no martensite phases, bainite phases or cementite phases in the ferrite or pearlite matrix.
The steel filament is provided with a coating promoting the adhesion with elastomer products, such as zinc or brass. The steel filament is drawn until a final diameter of less than 0.60 mm and has a final tensile strength of more than 1200 MPa.
The drawing of this low-carbon steel filament can be done without the intermediate patenting process and without any other heat treatment such as annealing because of the low carbon content.
The steel filament is directly drawn from wire rod of e.g. 5.5 mm diameter until a filament diameter of lower than 0.60 mm, resulting in a reduction in cross-sectional area of more than 98 per cent. With a final diameter equal to or lower than 0.45 mm, a reduction in cross-sectional area of more than 99 per cent has been realized.
Coating of e.g. brass can be done at an intermediate wire diameter between 5.5 mm and 0.60 mm. The brass coated steel wire is then further drawn, again without intermediate heat treatments, until its final filament diameter. The brass coating has a double function. First of all, in the final product, the brass promotes the adhesion with rubber by making sulphur bridges between the copper in the brass and the rubber. In the second place, brass being is a softer material than the low carbon steel, brass functions as a lubricant during the final drawing stages and allows the steel filament to be subjected to the above-mentioned high degrees of reduction in cross-sectional area. Due to this high deformability, high levels of final tensile strengths are obtainable.
Prior art document JP-A-05/105951 discloses a low carbon steel wire. This low carbon steel wire is, however, subjected to one or more intermediate heat treatments.
Prior art document U.S. Pat. No. 5,833,771 discloses a steel wire with a low carbon content for the reinforcement of tires. However, the steel wire has a stainless steel composition with, amongst other elements, e.g. between 6 and 10% nickel and between 16% and 20% chromium. This is not a plain carbon composition.
Prior art document WO-A-84/02354 discloses a high strength, low carbon steel rod and steel wire. However, this steel wire has a dual-phase steel composition with a ferrite matrix with a dispersed second phase such as martensite, bainite and/or austenite. This dual phase steel is different from a plain carbon steel.
According to a second aspect of the present invention, there is provided a steel cord having one or more low-carbon steel filaments according to the first aspect of the present invention.
Preferably, the steel cord consists of only low-carbon steel filaments according to the first aspect of the invention.
Examples of suitable steel cord constructions are all steel cord constructions which are suitable for the reinforcement of the breaker or belt layer of tires: 2×1, 3×1, 4×1, 5×1, 1+4, 1+5, 1+6, 2+2, 3+2, 2+3.
According to a third aspect of the present invention, there is provided a method for manufacturing a steel filament adapted for the reinforcement of elastomer products. The method comprises the following steps:
The coating can be provided at final filament diameter or, preferably, at an intermediate diameter, as has been explained here above.
These process steps a. to c. may be followed by a process step of twisting various such low carbon filaments with each other or with other filaments to form a steel cord.
By avoiding the intermediate heat treatments up to more than 3% savings could be made in CO2 production in comparison with the prior art situation.
According to a fourth aspect of the present invention, the low-carbon steel filaments according to the first aspect of the invention or the low-carbon steel cords according to the second aspect of the invention, are used in an elastomer or thermoplastic product.
Suitable elastomer products are tires, conveyor belts, timing belts, hoses, flexible pipes, etc. Suitable thermoplastic products are impact beams and flexible hoses.
The invention steel filament (first aspect) and the invention steel cord (second aspect) are particularly suitable for the reinforcement of the breaker or belt layer of a tire. Although lacking tensile strengths above 2000 MPa, the low carbon filaments and low carbon steel cords according to the invention provide the breaker or belt layer of a tire the required degree of stiffness.
A steel cord according to the invention can be made as follows.
Starting product is a wire rod with a plain carbon composition with a carbon content ranging between 0.04 wt % and 0.08 wt %. The complete composition of the wire rod is as follows: a carbon content of 0.06 wt %, a silicon content of 0.166 wt %, a chromium content of 0.042 wt %, a copper content of 0.173 wt %, a manganese content of 0.382 wt %, a molybdenum content of 0.013 wt %, a nitrogen content of 0.006 wt %, a nickel content of 0.077 wt %, a phosphorus content of 0.007 wt %, a sulphur content of 0.013 wt %.
Generally, as mentioned the silicon content is below 1.0 wt %, the manganese content below 2.0%. Furthermore, the amounts of Cr, Cu, Ni and Mo are limited to 0.20%. The amounts of phosphorus and sulphur are limited to 0.030 wt %. The amount of N is limited to 0.015%.
The wire rod is dry drawn from the wire rod diameter of 5.5 mm until an intermediate diameter of 2.0 mm.
At this intermediate diameter of 2.0 mm, copper is first electroplated on the steel wire e.g. in a Cu-pyrophosphate bath, then zinc is electroplated on the steel wire e.g. in a ZnSO4 bath, and thereafter a thermodiffusion treatment is applied in order to provide a brass coating on the wire.
The thermodiffusion involves heating up to a temperature of 450° C. to 600° C. This treatment, however, only lasts a few seconds. This temperature is not as elevated as the austhenitizing temperature. Moreover, the thermodiffusion does not realize a change in metal structure of the steel wire.
No patenting takes place at this intermediate diameter. Similarly, no other heating treatment such as annealing takes place at this intermediate diameter.
As an alternative to brass, the steel wire can be electroplated with zinc.
Coming back to the brass coating, the brass coated steel wire of 2.0 mm is then wet drawn until a final filament with a final diameter of 0.45 mm of 1400 MPa.
Finally, several such low-carbon 0.45 filaments are twisted into a 1+5×0.45 steel cord. This low-carbon steel cord has a breaking load of 1270 Newton.
Other examples of an invention cord are:
3+2×0.45
1+4×0.45
In case the steel wire has been electroplated with zinc, a silane primer can be applied to the twisted steel cord in the following way. After an optional cleaning operation, the steel cord may be coated with a primer selected from organo functional silanes, organo functional titanates and organo functional zirconates which are known in the art for said purpose. Preferably, but not exclusively, the organo functional silane primers are selected from the compounds of the following formula:
Y—(CH2)n—SiX3
wherein:
Y represents an organo functional group selected from —NH2, CH2═CH—, CH2═C(CH3)COO—, 2,3-epoxypropoxy, HS— and, Cl—
X represents a silicon functional group selected from —OR, —OC(═O)R′, —Cl wherein R and R′ are independently selected from C1 to C4 alkyl, preferably —CH3, and —C2H5; and
n is an integer between 0 and 10, preferably from 0 to 10 and most preferably from 0 to 3.
The organo functional silanes described above are commercially available products.
By applying the process according to the invention, a saving of 70 kg CO2 per Ton of steel cord has been realized. As a result the carbon footprint of the invention steel cord has decreased in comparison with prior art steel cords.
| Number | Date | Country | Kind |
|---|---|---|---|
| 08152265 | Mar 2008 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2009/052216 | 2/25/2009 | WO | 00 | 9/2/2010 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2009/109495 | 9/11/2009 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 3502513 | Rice et al. | Mar 1970 | A |
| 4255496 | Haemers | Mar 1981 | A |
| 4613385 | Thomas et al. | Sep 1986 | A |
| 5141570 | Yutori et al. | Aug 1992 | A |
| 5833771 | Arnaud et al. | Nov 1998 | A |
| 5843583 | D'Haene et al. | Dec 1998 | A |
| 20050079364 | van Ooij et al. | Apr 2005 | A1 |
| 20080041503 | Torizuka et al. | Feb 2008 | A1 |
| Number | Date | Country |
|---|---|---|
| 5-105951 | Apr 1993 | JP |
| 2003321742 | Nov 2003 | JP |
| WO 8402354 | Dec 1982 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20110000593 A1 | Jan 2011 | US |
