JPH10100314A - Polyethylene resin coated steel material - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a polyethylene resin coated steel material equipped with cold heat cycle characteristic resistance in addition to cathode electrolytic release resistance. SOLUTION: This polyethylene resin coated steel material is obtained by successively laminating a chromate treatment layer, an epoxy primer layer, a modified polyethylene adhesive resin layer and a polyethylene corrosion-proof resin layer to the surface of a steel material. In this case, the film thickness of the epoxy primer layer is 10-100μm and the density AD of the modified polyethylene adhesive resin layer and the density PD of the polyethylene corrosion-proof resin layer satisfy formula -5.714×PD<2> +10.287×PD-3.666>=AD>=5.155×PD<2> -10.222×PD+5.951. The densities AD, PD are a value displayed by a unit of g/cm<3> .

Description

Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polyethylene resin-coated steel material having excellent resistance to thermal cycling and resistance to cathodic electrolytic peeling. 2. Description of the Related Art Steel materials used in harsh environments such as humid environments such as soil and seawater, and marine environments where ice blocks and driftwood repeatedly collide are coated with a polyethylene resin having both high corrosion resistance and strength. Often done. The coating layer of such a polyethylene resin-coated steel material is usually composed of four layers. That is, in order from the steel material side, a very thin chromate treatment layer directly applied to the steel material, an epoxy primer layer having a thickness of several tens to several hundreds μm, a modified polyethylene adhesive resin layer of about 0.1 to 0.5 mm, and 1-5mm thickest
It consists of four layers of polyethylene anticorrosive resin layer of a degree. Among these, the modified polyethylene adhesive resin layer has a role of bonding the polyethylene anticorrosion resin layer to the underlying epoxy primer layer. [0003] By applying such a four-layer coating, the polyethylene resin coating does not peel off for a long period of time in a normal environment and maintains high corrosion resistance. However, under the following use conditions, peeling occurs and progresses even in the above-mentioned four-layered polyethylene resin-coated steel material. [0004] First, there is a phenomenon that when the cathodic protection is performed, the peeling of the polyethylene resin layer is promoted. Since steel sheet piles, steel pipe piles, line pipes, and the like are used without repair for a long period of several decades or more, the cathodic protection method is applied in combination with corrosion protection by polyethylene resin coating.
In the case of construction, if the polyethylene resin has a flaw reaching the steel surface, the steel is protected by the effect of cathodic protection, but the polyethylene resin coating is for cathodic protection,
Rather, peeling is promoted. This phenomenon is known as "cathode electrolysis" in which an alkali is generated by the anticorrosion current, and the polyethylene resin layer is separated due to the alkali. Here, “cathodic protection” refers to a corrosion protection method in which the potential of a steel material is lowered to a potential at which corrosion occurs and the potential of an invariable region is obtained. There are two methods, a method using a sacrificial anode and a method using forced energization. is there. Usually, in a line pipe or the like, a method by forced energization is adopted from the viewpoint of simplicity. [0005] In recent years, in line pipes and the like, a method of heating heavy oil has been adopted in order to increase the fluidity of heavy oil in the pipe and improve the transport capacity, and the temperature thereof has been increasing. . At a high temperature, a small amount of water or ions permeates the polyethylene resin from the outside, and the permeated minute amounts of water or ions further promote peeling of the polyethylene resin coating. [0006] With such a rise in temperature, it has become an important issue for polyethylene resin-coated steel materials used in line pipes to also have cathodic electrolytic peeling resistance at high temperatures. In the following description, “cathode electrolytic peeling resistance at high temperature” is simply referred to as “cathode electrolytic peeling resistance”. Further, the use environment of the polyethylene resin-coated steel material is expanded to a wide temperature range from a cold region to a tropical region, and particularly when the temperature of the temperature is large in a desert region, such as a desert region, the steel material and the polyethylene are subjected to the cooling and heating cycle. Peeling from the resin coating becomes a problem. For this reason, it is necessary for line pipes and the like used in desert areas to have cold-heat cycle resistance. [0008] The measures taken so far for the above problems are limited to the following. As a measure for improving the cathodic electrolytic peeling resistance, for example, a mixed solution of phosphoric acid and chromic anhydride is partially reduced with an organic reducing agent, and silica-based fine particles and a silane coupling agent are added. A method using the obtained chromate treatment solution has been proposed (JP-A-3-234527). [0010] Further, as a method of improving the cathodic electrolytic stripping resistance, a polyethylene-coated steel material having an epoxy primer layer comprising an epoxy resin containing a phenol novolak type glycidyl ether, a dicyandiamide-based curing agent, an imidazole-based curing agent, and an inorganic pigment is also used. (JP-A-3-126550). However, these methods are intended to improve the resistance to cathodic electrolytic peeling by improving the chromate-treated layer or the epoxy primer layer, but do not take into account the thermal cycling resistance. A polyethylene resin-coated steel material having not only cathodic electrolytic peeling resistance but also good cooling and heat cycling characteristics and a good balance of all performances has not yet been developed. SUMMARY OF THE INVENTION It is an object of the present invention to provide a polyethylene resin-coated steel material having not only cathodic electrolytic peeling resistance but also cooling and heat cycling characteristics. Means for Solving the Problems In order to solve the above-mentioned problems, the present inventors have made a chromium-treated layer, an epoxy primer layer, a modified polyethylene adhesive resin layer and a polyethylene As a result of repeated investigations on a polyethylene-coated steel material obtained by sequentially laminating an anticorrosion resin layer, the following items could be confirmed. (A) When the density of the modified polyethylene adhesive resin layer is low and within a certain range in relation to the density of the polyethylene anticorrosion resin layer, the cycle resistance to cold and heat is improved. (B) However, if the density of the modified polyethylene adhesive resin is too low, the resistance to cathodic electrolytic peeling deteriorates. The present inventors have repeated detailed experiments by changing the densities of the modified polyethylene adhesive resin layer and the polyethylene anticorrosion resin layer, which have not been noticed so far, and as a result, the above (a) and ( The range of b) was successfully formulated. The present invention has been completed after further confirming these effects based on the technical idea expressed by the mathematical formula. The gist of the present invention is the following polyethylene resin-coated steel material. "A polyethylene-coated steel material in which a chromate treatment layer, an epoxy primer layer, a modified polyethylene adhesive resin layer, and a polyethylene anticorrosion resin layer are sequentially laminated on the surface of a steel material, and the epoxy primer layer has a thickness of 10 μm.
A polyethylene resin-coated steel material which is not less than 100 μm and whose relationship between the density AD of the modified polyethylene adhesive resin layer and the density PD of the polyethylene anticorrosion resin layer satisfies the following expression. -5.714 × PD ² + 10.287 × PD-3.666 ≧ AD ≧ 5.155 × PD ² -10.222 × PD + 5.951 ... However, both density, AD and PD are expressed in units of g / cm ^3. Value. ] The "thickness of the epoxy primer layer" is the weight method,
It means the average film thickness that can be measured with an electromagnetic thickness gauge or the like. Therefore, the top part (convex part) of the surface irregularities after blasting
The film thickness which varies depending on micro-positions such as the film thickness from the surface to the surface of the epoxy primer layer (minimum film thickness) or the film thickness from the bottom (recess) to the surface of the epoxy primer layer (maximum film thickness) does not apply. . In the above, the "density of the modified polyethylene adhesive resin layer and the polyethylene anticorrosion resin layer" is a density in a state where additives such as a pigment, an antioxidant and an ultraviolet absorber are not contained. FIG. 1 is a drawing showing the range of the density AD of the modified polyethylene adhesive resin and the density PD of the polyethylene anticorrosive resin satisfying the above formula. In the following description, FIG.
Curve 1 (Curve: AD = -5.714 × PD ² + 10.287 × PD-3.
666) is called the limit line of the thermal cycle characteristics, and the curve 2 (curve: AD = 5.155 × PD ² -10.222 × PD + 5.951) is called the cathodic electrolytic stripping limit line. Next, the reasons for limiting the present invention will be described in detail. 1. Steel Material First, the steel material used in the present invention may be a high alloy steel such as carbon steel, low alloy steel, and stainless steel. The shape of the steel material is not particularly limited, and may be a tubular material such as a line pipe or a steel pipe pile, or a shape such as a steel sheet pile. Prior to performing the chromate treatment, the outer surface of the steel material is subjected to conventional physical means such as known shot blasting, grid blasting and sand blasting, or chemical means such as pickling and alkali degreasing. Preferably, the surface is cleaned by appropriate combination. 2. The surface of the chromate-treated steel material is generally subjected to a chemical conversion treatment (chromate treatment, zinc phosphate treatment) as a base treatment in order to enhance adhesion and corrosion resistance. In the present invention, the chromate treatment is performed. Of these, the silica-based coating type chromate treatment is a desirable undercoating method because it has excellent workability and high primary adhesion. Further, a material subjected to a high reduction chromate treatment using an organic reducing agent may be applied, which is suitable for improving cathodic electrolytic peeling resistance. The chromate treatment layer is a layer formed by applying a chromate treatment agent to the surface of a cleaned steel material by a known method such as ironing or air spraying. The adhesion amount is 50 to 1000 m as the total chromium amount.
It is preferably in the range of g / m ² . If the amount of chromium adhered is less than 50 mg / m ² , the cathodic electrolytic peeling resistance is inferior, while if it exceeds 1000 mg / m ² , the chromate film itself becomes too thick, and the thermal cycling characteristics and the primary adhesion may decrease. . 3. Epoxy Primer Layer The epoxy primer layer is formed by using a known epoxy resin and a curing agent as main components, and optionally adding a pigment. Typical epoxy resins include bisphenol A, phenol novolak type, and the like, and examples of curing agents include amine-based curing agents, dicyandiamide-based curing agents, and imidazole curing agents. Latent curable one-part thermosetting epoxy primers with microencapsulated agents can also be used.
An active energy-curable epoxy primer obtained by mixing an unsaturated epoxy ester, an acrylate monomer and a polymerization initiator can also be used. In the polyethylene resin-coated steel material of the present invention, the thickness of the epoxy primer layer is from 10 μm to 100 μm.
It is essential that it is less than μm, more preferably 10 μm.
It is not less than μm and not more than 50 μm. When the thickness of the epoxy primer is less than 10 μm, the area of the very thin portion of the epoxy primer at the top portion after the blasting process becomes large, and the cathodic electrolytic peeling resistance is significantly reduced. On the other hand, since the residual stress generated during the curing process of the epoxy primer layer acts in the direction of peeling the epoxy primer, if the film thickness exceeds 100 μm, regardless of the densities of the modified polyethylene adhesive resin and the polyethylene anticorrosion resin described below, cold heat resistance The cycle characteristics are significantly reduced. 4. Modified polyethylene adhesive resin layer and polyethylene anticorrosion resin layer The densities of the modified polyethylene adhesive resin layer and the polyethylene anticorrosion resin layer used in the present invention satisfy the relationship represented by the above formula. In FIG. 1, when the density AD of the modified polyethylene adhesive resin is equal to or lower than the limit line 1 of the thermal cycle characteristic, that is, when the relationship AD ≦ -5.714 × PD2 + 10.287 × PD-3.666 is satisfied, the thermal cycle resistance characteristic is Will be excellent. When the density of the modified polyethylene adhesive resin layer exceeds the thermal cycle limit line 1, the internal stress of the modified polyethylene adhesive resin layer and the polyethylene anticorrosion resin layer increases when subjected to a thermal cycle, and the modified polyethylene adhesive resin layer or Either one or both of the polyethylene anticorrosion resin layers cannot reduce the stress during the thermal cycle. Such an increase in internal stress in the resin acts in the direction of peeling the polyethylene anticorrosive resin layer,
This leads to a decrease in the thermal cycling resistance. On the other hand, the density of the modified polyethylene adhesive resin layer
When AD is equal to or higher than the cathodic electrolytic peeling limit line 2, that is, AD
When the relationship of ≧ 5.155 × PD ² −10.222 × PD + 5.951 is satisfied, the cathodic electrolytic peeling resistance is excellent. Cathodic electrolytic peeling is a phenomenon in which the chromate or the vicinity of the primer peels off due to alkali generated by the cathode reaction 2H ₂ O + O ₂ + 4e ⁻ → 4OH ⁻ during cathodic protection. Water (H ₂ O) and oxygen (O ₂ ) involved in this reaction mainly pass through the polyethylene anticorrosive resin layer and the modified polyethylene adhesive resin layer to promote cathodic electrolytic peeling near the chromate or primer. . When the density AD is equal to or greater than the cathodic electrolysis peeling limit line 2, the minimum permeation of water and oxygen necessary for this reaction is suppressed by the modified polyethylene adhesive resin layer and the polyethylene anticorrosion resin layer, and as a result, Is greatly improved. As the modified polyethylene adhesive resin layer that can be used in the present invention, maleic anhydride-modified polyethylene is preferable because it exhibits particularly high adhesiveness.
An ethylene copolymer (eg, ethylene / vinyl acetate copolymer) -based resin, acrylic acid, or carboxylic acid-modified polyethylene resin can also be used. Further, the modified polyethylene adhesive resin may further contain a known coloring pigment. The thickness of the modified polyethylene adhesive resin layer is generally about 0.1 to 0.5 mm. As the polyethylene anticorrosive resin layer, any of polyethylenes generally used for coating steel materials can be used as long as the above-mentioned density range is satisfied. For example, low-density, medium-density, or high-density polyethylene may be used, and a small amount of another olefin or vinyl monomer (eg, propylene, vinyl acetate, acrylate, etc.) may be copolymerized. Is also good. In addition, additives such as conventional antioxidants, ultraviolet absorbers, pigments, fillers and the like may be added to the above polyethylene. The thickness of the polyethylene anticorrosion resin layer is preferably 1 mm to 5 mm from the viewpoint of mechanical strength and economy. The coating of the modified polyethylene adhesive resin and the polyethylene anticorrosive resin can be carried out by a conventional method using co-extrusion coating of a molten round die or extrusion coating of a molten T-die. Next, the effects of the present invention will be described with reference to examples. A 216 mm diameter carbon steel pipe for piping (JIS G 3452) was used as a steel material, and the surface was adjusted to a rust removal degree Sa3 by grid blasting before chromate treatment. Next, the steel pipe was heated to 60 ° C. by an induction heating device and subjected to a chromate treatment while moving on a transport roll at a pipe moving speed of 3 m / min so that the total chromium deposition amount was 250 mg / m ² . The chromate used was Cosmer 100 (manufactured by Kansai Paint Co., Ltd.) diluted with water. Thereafter, as the epoxy primer, a two-pack type amine cured epoxy primer (Nippon Paint No.
66 epoxy primer) was applied so as to have a film thickness shown in Table 1, and was cured by heating with an induction heating device. Table 1 shows the thickness of the epoxy primer layer, and the thickness and density of the modified polyethylene adhesive resin layer and the polyethylene anticorrosion resin layer described later. [Table 1] The numbers underlined in FIG. 1 indicate the test numbers in Table 1. In Comparative Examples, except for Test Nos. 20 and 21, it can be seen that the densities of the modified polyethylene adhesive resin layer and the polyethylene anticorrosion resin layer are out of the range of the present invention. In Test Nos. 20 and 21, the densities of the modified polyethylene adhesive resin layer and the polyethylene anticorrosion resin layer are both within the range of the present invention, but the film thickness is out of the range of the present invention. Table 1 shows the steel pipes subjected to the undercoating treatment.
The polyethylene anticorrosive resin layer of which density was similarly changed was coated via the maleic anhydride-modified polyethylene adhesive resin layer of which density was changed as shown in (1) to obtain an outer surface polyethylene coated steel pipe. 150 m from the above polyethylene coated steel pipe
The following cathodic electrolytic peeling test was performed on a sample cut into a length of m and a width of 70 mm. An artificial flaw reaching a steel surface with a diameter of 5 mm was provided on the coating layer of the test piece,
It was brought into contact with a 3% NaCl saline solution kept at 0 ° C., kept at a potential of −1.5 V with respect to a saturated calomel electrode, kept for 60 days, measured the peeling distance from the artificial flaw, and measured the cathode peeling length. Was used as an evaluation index. As an evaluation of the thermal cycling resistance,
The following test was performed using a test piece having the same shape as the above-mentioned cathodic electrolytic peelability test. That is, a heat cycle of holding at −45 ° C. for 8 hours and then holding at 80 ° C. for 16 hours was defined as one cycle, and a 20-cycle cooling / heating cycle was applied. Thereafter, a peeled area ratio (150 mm length × 70 mm width specimen) (Area ratio to an area of 10500 mm ² ) was measured. The relative humidity was maintained at 95% during the 16-hour hold at 80 ° C. in the cooling and heating cycle. The results of these tests are also shown in Table 1. As shown in Test Nos. 1 to 19, which are examples of the present invention, the thickness of the epoxy primer is 10 μm or more and 100 μm or more.
When the density is not more than μm and the density AD of the modified polyethylene adhesive resin layer and the density PD of the polyethylene anticorrosion resin layer satisfy the relationship of the above formula, it is understood that both the cathodic electrolytic peeling resistance and the thermal cycling resistance are excellent. On the other hand, as shown in Test No. 20 of the comparative example, when the thickness of the epoxy primer is less than 10 μm, the cathodic electrolytic peeling resistance decreases. As can be seen from Test No. 21, when the thickness of the epoxy primer exceeds 100 μm, the cathodic electrolytic peeling resistance is excellent, but the thermal cycling resistance is significantly deteriorated. As shown in Test Nos. 22 to 25, the density AD of the modified polyethylene adhesive resin layer was less than the cathodic electrolytic peeling limit line 2
In the case where AD is smaller than 5.155 × PD ² -10.222 × PD + 5.951, the resistance to cold and heat is excellent, but the resistance to cathodic electrolytic peeling is reduced. As shown in Test Nos. 26 to 29,
The density AD of the modified polyethylene adhesive resin layer exceeds the thermal cycle characteristic limit line 1, and is -5.714 × PD ² + 10.287 × PD-3.666.
<AD has excellent cathodic electrolytic peeling resistance, but has poor thermal cycling resistance. The polyethylene resin-coated steel material of the present invention
By controlling the film thickness of the epoxy primer layer and the densities of the modified polyethylene adhesive resin layer and the polyethylene anticorrosion resin layer, a superior balance between unprecedented excellent cold-heat cycling properties and cathodic electrolytic peeling properties is achieved. INDUSTRIAL APPLICABILITY The present invention is suitable as a material for steel sheet piles, steel pipe piles, pipes used particularly under severe environmental conditions, line pipes and the like that are heated in order to increase the fluidity of crude oil, and even in an environment where temperature changes drastically. Excellent corrosion resistance can be maintained without peeling of the polyethylene resin layer.

BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 shows a range to be satisfied by the density AD of the modified polyethylene adhesive resin and the density PD of the polyethylene anticorrosion resin in the present invention. [Explanation of Signs] 1 ... Limit line of thermal cycle characteristics 2 ... Limit line of cathodic electrolytic peeling 3 ... Density AD of modified polyethylene adhesive resin layer satisfying the formula
Range of density PD of polyethylene and polyethylene anticorrosion resin layer

Claims (1)

Claims 1. A polyethylene-coated steel material in which a chromate treatment layer, an epoxy primer layer, a modified polyethylene adhesive resin layer, and a polyethylene anticorrosion resin layer are sequentially laminated on the surface of a steel material, wherein the thickness of the epoxy primer layer is 10 µm or more. 100
A polyethylene resin-coated steel material having a diameter of not more than μm and a relationship between a density AD of the modified polyethylene adhesive resin layer and a density PD of the polyethylene anticorrosion resin layer satisfying the following expression. -5.714 × PD ² + 10.287 × PD-3.666 ≧ AD ≧ 5.155 × PD ² -10.222 × PD + 5.951 ... However, both AD and PD are values expressed in units of g / cm ^3. .