Patent Application
20230383391
The present invention relates to a coating intended for the protection, against molten metal corrosion, of cast iron used as parts in the hot-dip coating process of steel strips. The present invention also relates to the method for the manufacture of the coated cast iron thereof and to the process of hot dip coating with recourse to the coated cast iron thereof.
Usually, in the steel route production, steel strips are coated with a metallic coating deposited by hot-dip coating, i.e. hot-dip galvanizing or hot-dip aluminizing. This metallic coating contains elements typically selected notably among Zinc, Aluminium, Silicon, Magnesium . . . . These elements are melted in a bath through which the steel strip runs. To do so, some metallic devices or parts, such as the snout, the sink roll, the stabilizing rolls, pipelines or pumping elements are in direct contact with the molten bath.
During such contact, a reaction takes place between the molten metal and the immersed part. In particular, Zn and/or Al form intermetallic compounds with the iron of the metallic device, which results in an embrittlement of the immersed part. To limit this corrosion induced by the molten metal, the metallic devices or parts to be used in contact with the molten metal can be made of stainless steel. Despite the improvement of the resistance to molten metal corrosion, the stainless steel in contact with the molten metal keeps corroding, which leads to deformations, embrittlements and breakdowns. Stainless steels with a higher corrosion resistance can be considered but they are very expensive and will corrode anyhow. For this reason, some devices or parts in direct contact with the molten metal are simply made of cast iron. As cast iron corrodes rapidly, these devices or parts must be inspected and replaced very often. These regular replacements are done at the expense of line stops, which seriously impair the production of hot-dip coated steel strips.
is an object of the present invention to provide a cast iron substrate well protected against molten metal corrosion so that inspections and replacements are limited and so that embrittlement, deformation and breakdowns are further prevented. Moreover, another alternate or additional object of the invention is to provide an easy-to-implement method for producing this cast iron substrate without replacing the current equipment in the hot-dip galvanizing lines and hot-dip aluminizing lines.
The present invention provides a coated cast iron substrate comprising a coating comprising nanographites and a binder being sodium silicate, wherein the cast iron substrate has a composition, in weight percent, comprising from 2.0 to 6.67% C and comprising optionally one or more of the following elements:
The coated cast iron substrate according to the invention may also have the optional features listed below, considered individually or in combination:
The present invention also provides a method for the manufacture of a coated cast iron substrate comprising the successive following steps:
The method for the manufacture of the coated cast iron substrate according to the invention may also have the optional features listed below, considered individually or in combination:
The present invention also provides a process of hot dip coating a steel strip comprising a step of moving the steel strip through a molten metal bath comprising a piece of equipment at least partially immersed in the bath wherein at least a part of the piece of equipment is made of a coated cast iron substrate according to the invention.
Further, the present invention provides a hot dip coating facility comprising a molten metal bath comprising a piece of equipment at least partially immersed in the bath wherein at least a part of the piece of equipment is made of a coated cast iron substrate according to the invention.
The piece of equipment of the hot dip coating facility is optionally selected among a snout, an overflow, a sink roll, a stabilizing roll, a roll supporting arm, a roll flange, a pipeline and a pumping element.
To illustrate the invention, various embodiments and trials of non-limiting examples will be described, particularly with reference to
Other characteristics and advantages of the invention will become apparent from the following detailed description of the invention.
The following terms are defined:
Preferably, the width size of the nanographites is between 2 and 15 μm. Advantageously, the thickness of the nanographites is between 1 nm and 100 nm, more preferably between 1 and 50 nm, even more preferably between 1 and 10 nm.
Without willing to be bound by any theory, it seems that a coating comprising nanographites and a binder being sodium silicate on the cast iron substrate acts like a barrier to molten metal attack and prevents the formation of Zn-Fe and/or Al—Fe intermetallic compounds. Indeed, the coating according to the present invention is non-wetting with regard to the elements of the molten metal bath due to its graphitic content. In particular, it seems that nanographites are not wetted by liquid Zinc and/or Aluminium. The nanographites thus act as the non-wetting agent while sodium silicate acts as binder and adhesion promoter to the cast iron surface. The non-adhesion of the molten metal elements to the cast iron surface leads to an increase of the corrosion resistance, a decrease of the deformation risk of the substrate and a longer lifetime of the substrate. Moreover, the coating comprising sodium silicate well adheres on the cast iron substrate so that the cast iron substrate is even more protected. It further prevents the risk of coating cracks and coating detachment, which would expose the cast iron substrate to molten metal attack and deformation.
These advantages of the coating according to the invention are provided in all kinds of molten bath compositions in use on hot-dip coating lines. The molten metal bath composition can be zinc-based. Examples of zinc-based baths and coatings are: zinc comprising 0.2% of Al and 0.02% of Fe (HDG coating), zinc alloy comprising 5 wt. % of aluminium (Galfan® coating), zinc alloy comprising 55 wt. % of aluminium, about 1.5 wt. % of silicon, the remainder consisting of zinc and inevitable impurities due to the processing (Aluzinc®, Galvalume® coatings), zinc alloy comprising 0.5 to 20% of aluminium, 0.5 to 10% of magnesium, the remainder consisting of zinc and inevitable impurities due to the processing, zinc alloys comprising aluminium, magnesium and silicon, the remainder consisting of zinc and inevitable impurities due to the processing.
The molten metal bath composition can be also aluminium-based. Examples of aluminium-based baths and coatings are: aluminium alloy comprising from 8 to 11 wt. % of silicon and from 2 to 4 wt. % of iron, the remainder consisting of aluminium and inevitable impurities due to the processing (Alusi® coating), aluminium (Alupur® coating), aluminium alloys comprising zinc, magnesium and silicon, the remainder consisting of aluminium and inevitable impurities due to the processing.
The substrate is cast iron comprising from 2.0 to 6.67 wt % C, the remainder of the composition being made of iron and inevitable impurities resulting from the elaboration.
The composition can also include additional alloying elements such as, up to 3 wt % Mn, up to 5 wt % Si, up to 2 wt % Mo, up to 2.5 wt % Cu, up to 2 wt % Ni, up to 3 wt % Cr, up to 0.5 wt % V, up to 0.3 wt % Zr, up to 0.01 wt % Bi, up to 0.1 wt % Mg, up to 0.04 wt % Ce.
The steel can also comprise possible impurities resulting from the elaboration. For example, the inevitable impurities can include without limitation: P, S, Al, Ti, Nb, W, Pb, B, Sb, Sn, Zn, As, La, N, Se, O, H, Co, Ge, Ga. For example, the content by weight of each impurity is inferior to 0.1 wt %.
The cast-iron substrate can be notably any piece or part to be immersed at least partially in a molten metal bath. Preferably, the cast iron substrate is a snout, an overflow, a sink roll, a stabilizing roll, a roll supporting arm, roll flanges, a pipeline or a pumping element or a part of these elements.
The cast iron substrate is at least partially coated with a coating comprising nanographites and a binder being sodium silicate.
The concentration of nanographites in the coating is preferably between 1% to 70% by weight of dry coating, more preferably between 5 and 70 wt %, even more preferably between 10 and 65 wt %. Such concentrations provide a good balance between non-adhesion of the molten metal elements on the coating and adhesion of the coating to the substrate.
Preferably, the nanographites contain more than 95% by weight of C and advantageously more than 99%.
The binder is sodium silicate. In other words, the binder is obtained from sodium silicate. This sodium silicate reacts during the drying phase so as to form rigid siloxane chains. It is believed that the siloxane chains get attached to the hydroxyl groups present on the surface of the cast iron substrate. It is also believed that the sodium silicate dissolved in the aqueous mixture applied on the substrate will penetrate in all the crevices from the substrate surface and, after drying, will become tough and vitreous therefore anchoring the coating to the substrate.
Sodium silicate refers to any chemical compound with the formula Na2xSiyO2y+x or (Na2O)x·(SiO2)y. It can notably be sodium metasilicate Na2SiO3, sodium orthosilicate Na4SiO4, sodium pyrosilicate Na6Si2O7, Na2Si3O7.
The concentration of sodium silicate in the coating is preferably between 35% to 95% by weight of dry coating, more preferably between 35 and wt %. Such concentrations provide a good balance between non-adhesion of the molten metal elements on the coating and adhesion of the coating to the substrate.
According to one variant of the invention, the coating further comprises additives, notably to improve its thermal stability and/or its abrasion resistance. Such additives can be selected among clay, silica, quartz, kaolin, aluminium oxide, magnesium oxide, silicon oxide, titanium oxide, Yttrium oxide, zinc oxide, aluminium titanate, carbides and mixtures thereof. Examples of clay are green montmorillonite and white kaolin clays. Examples of carbides are silicon carbide and tungsten carbide.
If additives are added, their concentration in the dry coating can be up to 40 wt % and is comprised preferably between 10 and 40 wt % and more preferably between 15 and 35 wt %. When green montmorillonite is added, the ratio between the graphene weight content and the green montmorillonite weight content is preferably comprised between 0.2 and 0.8.
According to one variant of the invention, the coating consists of nanographites, a binder based on sodium silicate and optional additives selected among clay, silica, quartz, kaolin, aluminium oxide, magnesium oxide, silicon oxide, titanium oxide, Yttrium oxide, zinc oxide, aluminium titanate, carbides and mixtures thereof.
Preferably, the dry thickness of the coating is between 10 and 250 μm. More preferably, it is between 110 and 150 μm. For example, the thickness of the coating is between 10 and 100 μm or between 100 and 250 μm.
Preferably, the coating does not comprise at least one element chosen from a surfactant, an alcohol, aluminum silicate, aluminum sulfate, aluminum hydroxide, aluminum fluoride, copper sulfate, lithium chloride and magnesium sulfate.
The invention also relates to a method for the manufacture of the coated cast iron substrate according to the present invention, comprising the successive following steps:
In step A), the cast iron substrate can be provided in any size, dimensions and shapes. It can notably be in the form of a strip, a sheet, a piece, a part, an element, a device, an equipment . . . . It can be flat or shaped by any means.
Preferably, in step B), the deposition of the coating is performed by spin coating, spray coating, dip coating or brush coating.
Advantageously, in step B), the aqueous mixture comprises from 40 to 110 g/L of nanographites. More preferably, the aqueous mixture comprises from to 60 g/L of nanographites.
Advantageously, in step B), the aqueous mixture comprises from 40 to of binder. Preferably, the aqueous mixture comprises from 50 to 70 g/L of binder.
Sodium silicate can be added to the aqueous mixture in the form of an aqueous solution. Sodium silicate may also be in a hydrated form, of general formula (Na2O)x(SiO2)y·zH2O, such as for example Na2SiO3 5H2O or Na2Si3O7 3H2O.
Advantageously, in step B), the ratio in weight of nanographites with respect to binder is between 0.05 and 0.9, preferably between 0.1 and 0.5.
According to one variant of the invention, the aqueous mixture of step B) further comprises additives, notably to improve the thermal stability and/or the abrasion resistance of the coating. Such additives can be selected among clay, silica, quartz, kaolin, aluminium oxide, magnesium oxide, silicon oxide, titanium oxide, Yttrium oxide, zinc oxide, aluminium titanate, carbides and mixtures thereof. Examples of clay are green montmorillonite and white kaolin clays. Examples of carbides are silicon carbide and tungsten carbide. Clays further help adapting the viscosity of the aqueous mixture to further facilitate its application. In this regard, when green montmorillonite is added, the ratio between the graphene weight content and the green montmorillonite weight content is preferably comprised between 0.2 and 0.8.
In a preferred embodiment, the coating is dried, i.e. is actively dried as opposed to a natural drying in the air, in a step C). It is believed that the drying step allows for an improvement of the coating adhesion since the removal of water is better controlled. In a preferred embodiment, in step C), the drying is performed at a temperature between 50 and 150° C. and preferably between 80 and 120° C. The drying can be performed with forced air.
Advantageously, in step C), when a drying is applied, the drying is performed during 5 to 60 minutes and for example, between 15 and 45 minutes.
In another embodiment, no drying step is performed. The coating is left to dry in the air.
The invention also relates to the use of a coated cast iron according to the present invention for the manufacture of a snout, an overflow, a sink roll, a stabilizing roll, a roll supporting arm, a pipeline or a pumping element.
The invention also relates to a process of hot dip coating a steel strip comprising a step of moving the steel strip through a molten metal bath comprising a piece of equipment at least partially immersed in the bath wherein at least a part of the piece of equipment is made of a coated cast iron substrate according to the invention.
The invention also relates to a hot dip coating facility comprising a molten metal bath comprising a piece of equipment at least partially immersed in the bath wherein at least a part of the piece of equipment is made of a coated cast iron substrate according to the invention.
The invention will now be explained based on trials carried out for information only. They are not limiting.
In the examples, the cast iron substrate having the following composition in weight percent was used:
For Trial 1, the cast iron substrate was coated by brushing an aqueous mixture comprising 50 g/L of nanographites having a lateral size between 2 to 10 μm, a width between 2 to 15 μm and a thickness between 1 to 100 nm and 60 g/L of sodium silicate, as a binder, in the form of an aqueous solution comprising wt % of SiO2 and 7.5-8.5 wt % of Na2O. Then, the coating was dried inside a furnace with hot air during 60 minutes at 75° C. The coating was 130 μm thick and comprised 45 wt % of nanographites and 55 wt % of binder.
For Trial 2, the cast iron substrate was coated by brushing an aqueous mixture comprising 50 g/L of nanographites having a lateral size between 2 to μm, a width between 2 to 15 μm and a thickness between 1 to 100 nm, 100 g/L of green montmorillonite clay and 60 g/L of sodium silicate, as a binder, in the form of an aqueous solution comprising 25.6-27.6 wt % of SiO2 and 7.5-8.5 wt % of Na2O. Then, the coating was dried inside a furnace with hot air during 60 minutes at 75° C. The coating was 130 μm thick and comprised 11 wt % of nanographite, 69 wt % of binder and 20 wt % of green montmorillonite clay.
For Trial 3, the cast iron substrate was coated by brushing an aqueous mixture comprising 90 g/L of nanographites having a lateral size between 2 to μm, a width between 2 to 15 μm and a thickness between 1 to 100 nm, and g/L of sodium silicate, as a binder, in the form of an aqueous solution comprising 25.6-27.6 wt % of SiO2 and 7.5-8.5 wt % of Na2O. Then, the coating was dried inside a furnace with hot air during 60 minutes at 75° C. The coating was 130 μm thick and comprised 60 wt % of nanographite, 40 wt % of binder.
For Trial 4, the cast iron substrate was coated by brushing an aqueous mixture comprising 50 g/L of reduced graphene oxide having a lateral size between 5 to 30 μm, a width between 5 to 30 μm and a thickness between 1 to nm and 60 g/L of sodium silicate, as a binder, in the form of an aqueous solution comprising 25.6-27.6 wt % of SiO2 and 7.5-8.5 wt % of Na2O. Then, the coating was dried inside a furnace with hot air during 60 minutes at 75° C. The coating was 130 μm thick and comprised 45 wt % of reduced graphene oxide and wt % of binder.
To evaluate the coating adhesion, an adhesive tape was deposited on the Trials and then removed. The coating adhesion was evaluated by visual inspection on the Trials: 0 means that all the coating has remained on the cast iron steel; 1 means that some parts of the coating has been removed and 2 means that almost all the coating has been removed.
The results are in the following Table 1:
Trials according to the present invention show an excellent coating adhesion.
Trials 1 to 3 were immersed 8 days in an aluminium-based bath comprising 10% of Si and 2.5% of Fe. After 8 days, a non-adherent metallic thin film was present on the Trials. The metallic film was easily peeled off from the Trials. The coating of the present invention was still present on both Trials. No attack of aluminium appeared.
The Trials according of the present invention were well protected against aluminium attack.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2020/060148 | 10/29/2020 | WO |
