JP5997427B2 - Weatherproof wire - Google Patents

Description

  The present invention relates to a weather-resistant electric wire coated with a polyvinyl chloride resin composition. Specifically, the present invention relates to a weather-resistant electric wire that can prevent UV degradation over a long period of time even when used outdoors by using a polyvinyl chloride resin composition as a sheath.

  Polyvinyl chloride is mainly used as a synthetic resin used for insulation of electric wires and cables. Since such polyvinyl chloride is inexpensive and can be easily processed by adding a plasticizer, it is widely used as an automotive part or a building member.

  Here, since high weather resistance is required when using polyvinyl chloride outdoors, a technique for improving the weather resistance of polyvinyl chloride has been disclosed (see, for example, Patent Documents 1 and 2). ). Patent Document 1 discloses a polyvinyl chloride resin composition that is improved in thermal stability and weather resistance by adding a Ca-Zn stabilizer, hydrotalcite, and hydrophobic silica to a polyvinyl chloride resin. Yes. Patent Document 2 discloses a weather resistant flame retardant resin composition containing a base polymer, a metal hydrate, a high molecular weight hindered amine light stabilizer, a low molecular weight hindered amine light stabilizer, and an ultraviolet absorber. An electric wire coated with a resin composition is also disclosed.

JP-A-6-80849 JP 2005-187595 A

  However, although the polyvinyl chloride resin composition described in Patent Document 1 also has high weather resistance, further weather resistance is necessary to ensure insulation over a long period of time. Moreover, in the flame-retardant resin composition described in Patent Document 2, the weather resistance is improved by adding a light stabilizer or an ultraviolet absorber, but the weather resistance is insufficient when used outdoors. . Furthermore, there is a problem in dispersibility of the light stabilizer and the ultraviolet absorber, and the mechanical strength may be lowered.

  The present invention has been made in view of the problems of such conventional techniques. An object of the present invention is to provide a weather-resistant electric wire that can maintain high weather resistance over a long period of time even when used outdoors.

The weather-resistant electric wire according to the first aspect of the present invention includes a conductor and a sheath layer that covers the conductor. The sheath layer is composed of 20 to 100 parts by weight of a plasticizer, 8 to 15 parts by weight of a hydrotalcite, 4 to 15 parts by weight of a Ca—Zn stabilizer, 100 parts by weight of titanium oxide, and 100 parts by weight of a polyvinyl chloride resin. 5 to 5.0 parts by weight, filler Tona Ru polyvinyl chloride resin composition obtained by blending.

  In the weatherable electric wire according to the second aspect of the present invention, in the cable of the first aspect, the polyvinyl chloride resin composition further includes a colorant, and the lightness of the Munsell color system in the sheath layer is 6. 0 or more.

  The weather-resistant electric wire of the present invention uses a vinyl chloride sheath that is highly blended with hydrotalcite and titanium oxide and has improved weather resistance while suppressing a decrease in mechanical strength. Therefore, even if it is used outdoors, it is possible to suppress ultraviolet ray degradation over a long period of time and to ensure insulation.

It is the schematic which shows the weatherproof electric wire which concerns on embodiment of this invention. (A) is sectional drawing of the said weather resistant electric wire, (b) is a perspective view of the said weather resistant electric wire.

  Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. In addition, the dimension ratio of drawing is exaggerated on account of description, and may differ from an actual ratio.

  A weather-resistant electric wire (weather-resistant cable) 1 according to an embodiment of the present invention includes a conductor 2 and a sheath layer 4 that covers the periphery of the conductor 2 as shown in FIG. Further, an insulator 3 is interposed between the conductor 2 and the sheath layer 4.

  As the conductor 2, well-known conductive metal materials such as copper, copper alloy, aluminum, and aluminum alloy can be used. Moreover, as the insulator 3, polyolefin resin, such as polyethylene and polypropylene, and polyvinyl chloride resin can be used. This insulator 3 covers the conductor 2 by extrusion molding. Polyolefin resins constituting the insulator 3 include polyethylene (PE), ethylene-vinyl acetate copolymer (EVA), ethylene-ethyl acrylate copolymer (EEA), ethylene-α-olefin copolymer, ethylene -A propylene copolymer etc. are mentioned. These have different characteristics, and can be used alone or in combination of a plurality of types as polyolefin resins.

  The sheath layer 4 contains a polyvinyl chloride resin composition containing a polyvinyl chloride resin, a plasticizer, a hydrotalcite, a Ca—Zn-based stabilizer, and titanium oxide. By adding hydrotalcite and titanium oxide to the polyvinyl chloride resin, a polyvinyl chloride sheath with improved weather resistance can be obtained without deteriorating the mechanical properties of the sheath layer 4.

  Examples of the polyvinyl chloride resin used for the sheath layer 4 include polyvinyl chloride, chlorinated polyvinyl chloride, polyvinylidene chloride, chlorinated polyethylene, vinyl chloride-vinyl acetate copolymer, and vinyl chloride-ethylene copolymer. , Vinyl chloride-propylene copolymer, vinyl chloride-styrene copolymer, vinyl chloride-isobutylene copolymer, vinyl chloride-vinylidene chloride copolymer, vinyl chloride-styrene-maleic anhydride copolymer, vinyl chloride-styrene -Acrylonitrile copolymer, vinyl chloride-butadiene copolymer, vinyl chloride-isoprene copolymer, vinyl chloride-chlorinated propylene copolymer, vinyl chloride-vinylidene chloride-vinyl acetate copolymer, vinyl chloride-maleic acid ester Copolymer, vinyl chloride-methacrylate copolymer, vinyl chloride Acrylonitrile copolymer, vinyl chloride - may be mentioned various vinyl ether copolymers. The polymerization method of the polyvinyl chloride resin is not particularly limited, such as bulk polymerization, solution polymerization, suspension polymerization, and emulsion polymerization.

  Moreover, it is preferable that the average degree of polymerization of a polyvinyl chloride resin is 1200-2000. When the average degree of polymerization is 1200 or more, weather resistance can be secured to some extent. Moreover, when the average degree of polymerization is 2000 or less, an increase in melt viscosity during extrusion molding can be suppressed, and deterioration of thermal stability during molding processing can be prevented.

  Moreover, as a plasticizer, what is normally used for a polyvinyl chloride resin should just be used. That is, plasticizers such as phthalic acid, trimellitic acid, adipic acid, and polyester can be used. Among these, phthalic acid-based, trimellitic acid-based and adipic acid-based plasticizers are preferable, and phthalic acid-based and trimellitic acid-based plasticizers are most preferable. These may be used alone or in combination of two or more.

  In addition, as a plasticizer, the phthalic acid ester shown in Chemical Formula 1 is particularly preferable, and among them, diisononyl phthalate, diisodecyl phthalate, and diundecyl phthalate are preferably used. When such a phthalate ester is mixed with a polyvinyl chloride resin together with the hydrotalcite, Ca—Zn stabilizer and titanium oxide, a polyvinyl chloride resin composition having excellent processability such as fluidity and thermal stability. Can be obtained. In addition, as the plasticizer, not only a phthalate ester represented by Chemical Formula 1 but also a heat-resistant plasticizer such as trimellitic acid ester may be used. Even when trimellitic acid ester is used, a polyvinyl chloride resin composition having excellent processability can be obtained. Examples of trimellitic acid esters include trimellitic acid tris (2-ethylhexyl).

式中、ＲはＣ_ｎＨ_２ｎ＋１（ｎは９以上の整数）を示す。

In the formula, R represents C _n H _{2n + 1} (n is an integer of 9 or more).

Moreover, as a hydrotalcite, the compound shown by the following compositional | empirical formula (2) can be used.
Mg _1-x Al _x (OH) ₂ (CO ₃ ) _{x / 2} · mH ₂ O (2)
In the formula, X is a value satisfying 0 <x ≦ 0.5, and m is a positive number. The hydrotalcite may be a natural product or a synthetic product. As a natural product, for example, a compound represented by the molecular formula [Mg ₆ Al ₂ (OH) ₁₆ (CO ₃ ) ₃ · 4H ₂ O] can be used. As a synthetic product, for example, a molecular formula represented by [Mg _{4 .5} Al ₂ (OH) ₁₃ CO ₃ .3.5H ₂ O] can be used. Such hydrotalcite has the effect of improving the corrosivity and weather resistance of the polyvinyl chloride resin composition. In this embodiment, the crystal structure of hydrotalcite, the crystal particle diameter, and the presence or absence of crystal water are not limited.

  Furthermore, as Ca-Zn stabilizers, calcium salts of higher fatty acids such as 2-ethylhexylic acid, benzoic acid, isodecanoic acid, citric acid and sorbic acid, and higher fatty acids such as 2-ethylhexylic acid, isodecanoic acid and neodecanoic acid are used. Examples thereof include zinc salts. These can be used alone or in combination of two or more.

As titanium oxide, titanium (IV) (TiO ₂ ) can be used. Moreover, as a crystal structure of titanium oxide, both a rutile type and an anatase type can be used.

  Here, the deterioration of polyvinyl chloride is said to be due to the formation of polyene having a conjugated double bond by dehydrochlorination reaction caused by ultraviolet rays, or the formation of carboxylic acid and carboxyl group by oxidation reaction. ing. And since titanium oxide has the effect | action which absorbs the ultraviolet-ray whose wavelength is 400 nm or less, even when it uses outdoors, it can maintain high weather resistance by mix | blending with a polyvinyl chloride resin.

  In addition, since an ultraviolet-ray can be absorbed efficiently, so that the particle diameter of a titanium oxide is small, it is preferable that the average particle diameter of a titanium oxide shall be 0.5 micrometer or less. The dispersibility of the titanium oxide in a polyvinyl chloride resin composition can also be improved because it is 0.5 micrometer or less. In view of dispersibility and ultraviolet absorption efficiency, the average particle diameter of titanium oxide is more preferably 0.15 μm to 0.35 μm. Here, the average particle diameter of titanium oxide can be determined by a laser diffraction particle size distribution measuring apparatus. In addition, the average particle diameter in this case means a median diameter (D50).

  The content of each component in the polyvinyl chloride resin composition is 20 to 100 parts by weight of plasticizer, 8 to 15 parts by weight of hydrotalcite, and 4 to 5 parts of Ca-Zn stabilizer for 100 parts by weight of the polyvinyl chloride resin. It is preferable to use 15 parts by weight and 0.5 to 5.0 parts by weight of titanium oxide. By setting the contents of the plasticizer, hydrotalcite, Ca—Zn stabilizer and titanium oxide within such ranges, high weather resistance can be obtained while preventing the mechanical strength from being lowered. In addition, it is more preferable to mix | blend a plasticizer with 20-50 weight part with respect to 100 weight part of polyvinyl chloride resin, and a Ca-Zn type stabilizer is 4-6 with respect to 100 weight part of polyvinyl chloride resin. It is more preferable to blend parts by weight. Furthermore, it is more preferable that the hydrotalcite is blended in an amount of 10 to 15 parts by weight with respect to 100 parts by weight of the polyvinyl chloride resin. Thereby, the mechanical strength of the polyvinyl chloride resin composition can be further improved. Moreover, it is more preferable that 3 to 5 parts by weight of titanium oxide is blended with respect to 100 parts by weight of the polyvinyl chloride resin. Thereby, it becomes possible to absorb ultraviolet rays efficiently and to further improve the weather resistance of the polyvinyl chloride resin composition.

  If necessary, the polyvinyl chloride resin composition may contain a filler, a lubricant, a flame retardant, and a processing aid. As the filler, calcium carbonate, talc, clay and the like can be used. The blending amount of the filler can be appropriately selected according to demands such as manufacturing cost, insulation, shape retention and the like. As the lubricant, polyethylene wax, silicone oil, hydroxystearic acid and the like can be used. As the flame retardant, inorganic and organic flame retardants can be used. As the inorganic flame retardant, antimony trioxide, magnesium hydroxide, aluminum hydroxide, zinc borate, a phosphorus compound, or the like can be used. As the organic flame retardant, a halogen-based organic flame retardant such as chlorine or bromine can be used. As processing aids, petroleum oils such as paraffinic oils, aromatic oils or naphthenic oils added to rubber materials and the like can be used.

  Here, in conventional electric wires and cables, when the polyvinyl chloride sheath layer is light in color, exposure to ultraviolet rays such as outdoor use may cause bleeding phenomenon and mechanical strength decrease due to ultraviolet ray deterioration. It happened. In order to improve the weather resistance by preventing the occurrence of such bleed phenomenon and the decrease in mechanical strength, conventional colorants such as black, gray, blue and green that easily absorb ultraviolet rays are blended. There were many things to do. Therefore, since the conventional weather-resistant electric wires and cables are colored with the dark color as described above, there is a problem in design.

  However, in the weather resistant electric wire of the present embodiment, the sheath layer 4 is blended with titanium oxide having an ultraviolet absorbing action. Therefore, it is not necessary to use a dark colorant, and a light colorant such as ivory or beige can be used. Specifically, a colorant having a lightness of 6.0 or more in the Munsell color system can be used. As a result, the sheath layer in the weather-resistant electric wire of the present embodiment can also have a brightness of 6.0 or more in the Munsell color system while maintaining high weather resistance, so that the design can be improved. Become.

  As the colorant that can be mixed in the polyvinyl chloride resin composition of the sheath layer 4, general inorganic pigments and organic pigments described in "Pigment Handbook (Edited by Japan Pigment Technical Association)" can be used. Examples of inorganic pigments include (complex) metal oxides containing titanium such as titanium yellow, zinc oxide, iron oxide, zinc sulfide, and antimony trioxide. Examples of the organic pigment include phthalocyanine, anthraquinone, quinacridone, azo, isoindolinone, quinophthalone, perinone, and perylene pigments.

  The sheath layer 4 can be formed as follows. First, mix polyvinyl chloride resin, plasticizer, filler, Ca-Zn stabilizer, hydrotalcite and titanium oxide (colorants, fillers, lubricants, flame retardants, processing aids, etc., if necessary) And dry up. Then, the obtained mixture can be formed on the conductor 2 on which the insulator 3 is formed by extrusion molding. Moreover, the sheath layer 4 may consist only of the polyvinyl chloride resin composition, or may consist of a mixture of the polyvinyl chloride resin composition and another resin.

  EXAMPLES Hereinafter, although an Example and a comparative example demonstrate this invention further in detail, this invention is not limited to these Examples.

[Examples 1 to 18]
First, polyvinyl chloride resin, plasticizer, filler, Ca—Zn stabilizer, hydrotalcite, and titanium oxide in parts by weight shown in Tables 1 and 2 were mixed, and further a colorant was added and dried up. The obtained powdery mixture was roll-kneaded at 160 ° C. ± 10 ° C. for 8 minutes to obtain a kneaded sheet having a thickness of about 1.3 mm. This was further hot-pressed at 180 ° C. to produce sheets of each example having a thickness of 1.0 mm ± 0.15 mm.

[Comparative Examples 1 and 2]
A thickness of 1.0 mm ± 0.15 mm in the same manner as in Example except that polyvinyl chloride resin, plasticizer, filler, Ca—Zn-based stabilizer and hydrotalcite having the parts by weight shown in Table 3 were used. A sheet was produced.

[Comparative Examples 3 to 8]
Thickness 1.0 mm ± 0 in the same manner as in Example except that polyvinyl chloride resin, plasticizer, filler, Ca—Zn stabilizer, hydrotalcite and titanium oxide in parts by weight shown in Table 3 were used. A 15 mm sheet was prepared.

[Comparative Examples 9 and 10]
Thickness in the same manner as in Example except that polyvinyl chloride resin, plasticizer, filler, Ca-Zn stabilizer, hydrotalcite and ultraviolet absorber (UV agent) in parts by weight shown in Table 3 were used. A 1.0 mm ± 0.15 mm sheet was prepared.

  The polyvinyl chloride resin used in the examples and comparative examples is TK-1300 manufactured by Shin-Etsu Chemical Co., Ltd., and DINP and DOP as plasticizers are diisononyl phthalate and bis phthalate manufactured by J Plus Co., Ltd. (2-ethylhexyl) was used respectively. Furthermore, heavy calcium carbonate was used as a filler. As hydrotalcite, Alkamizer 2 (registered trademark) manufactured by Kyowa Chemical Co., Ltd. was used. In addition, as a UV absorber of Comparative Examples 9 and 10, VIONIL B manufactured by Seawater Chemical Research Co., Ltd. was used.

  Moreover, the color of the sheet | seat of the obtained Example and comparative example was confirmed by visual observation, and the result was shown to Tables 1 thru | or 3. Furthermore, when the brightness of the sheet | seat of each Example and the comparative example was measured using the colorimeter, all were 6.0 or more.

[Normal temperature tensile test]
The sheets obtained in Examples 1 to 18 and Comparative Examples 1 to 10 were subjected to a room temperature tensile test in accordance with Japanese Industrial Standard JISK7161. Specifically, the test pieces (JIS No. 3 dumbbell pieces) of each Example and Comparative Example were prepared by leaving the sheets of the above Examples and Comparative Examples to stand for 12 hours or more at room temperature (25 ° C.) and cutting them. And the test temperature was 23 ° C. ± 2 ° C., the tensile speed was 200 mm / min, and the tensile strength Ts and elongation rate E of the test piece were measured. This tensile test was performed on five test pieces, and the average values of the tensile strength and elongation of each test piece were taken as the tensile strength and elongation of each example and comparative example. And in Tables 1 to 3, the case where the average value of the tensile strength Ts of the test piece was over 18 MPa was “◯”, the case of 14-18 MPa was “Δ”, and the case of less than 14 MPa was “x”. . Further, the case where the average value of the elongation percentage E of the test piece was over 300% was “◯”, the case of 250 to 300% was “Δ”, and the case of less than 250% was “X”.

[Weather resistance test]
Using a sunshine weather meter WELL-SUM-DC (H) manufactured by Suga Test Instruments Co., Ltd., each sheet of the above Examples and Comparative Examples was irradiated with light. The temperature during light irradiation was 70 ° C. ± 1.5 ° C., and the humidity was 30 to 70 RH ± 5 RH. Then, the average value of the tensile strength and elongation rate of the test piece of each Example and comparative example after light irradiation was similarly calculated | required for the said normal temperature tension test. In Tables 1 to 3, the remaining ratio RTs of tensile strength after light irradiation with respect to tensile strength before light irradiation ([tensile strength after light irradiation] / [tensile strength before light irradiation] × 100) Is over 90%, "60", 60-90% is "△", less than 60% is "x". Further, the case where the residual ratio RE of the elongation after light irradiation with respect to the elongation before light irradiation ([Elongation after light irradiation] / [Elongation before light irradiation] × 100) is more than 90% is indicated by “◯”. In the case of 60 to 90%, “Δ” was set, and in the case of less than 60%, “X” was set. Tables 1 to 3 show RTs and RE when the light irradiation time is 1000 hours and 2000 hours .

  As shown in Tables 1 to 3, Examples 1 to 18 according to the present invention have a tensile strength of more than 18 MPa and an elongation of 300% in the room temperature tensile test despite the lightness being 6.0 or more. It was super. In the weather resistance test, RTs and RE exceeded 90%, indicating high weather resistance. On the other hand, in Comparative Examples 1 and 2 that do not contain titanium oxide and Comparative Examples 3 to 8 in which the content of titanium oxide is small, the ultraviolet light deterioration was severe and the weather resistance was greatly reduced.

  Further, when Comparative Examples 1 and 2 and Comparative Examples 9 and 10 were compared, the weather resistance was slightly improved by containing the UV agent, but there was a problem in dispersibility, and the mechanical strength was greatly reduced. On the other hand, in Examples 1-18, since not only titanium oxide but also hydrotalcite is highly blended, a decrease in mechanical strength is suppressed while improving weather resistance.

  Although the present invention has been described with reference to the examples and comparative examples, the present invention is not limited to these, and various modifications can be made within the scope of the gist of the present invention.

DESCRIPTION OF SYMBOLS 1 Weatherproof electric wire 2 Conductor 3 Insulator 4 Sheath layer

Claims (2)

Conductors,
A sheath layer covering the conductor;
With
The sheath layer is composed of 20 to 100 parts by weight of a plasticizer, 8 to 15 parts by weight of hydrotalcite, 4 to 15 parts by weight of a Ca—Zn stabilizer, 0.5 to 0.5 parts of titanium oxide based on 100 parts by weight of a polyvinyl chloride resin. 5.0 parts by weight, weather resistance wire, wherein the polyvinyl resin composition Tona Rukoto chloride by blending a filler. The polyvinyl chloride resin composition further includes a colorant,
The weather-resistant electric wire according to claim 1, wherein the lightness of the Munsell color system in the sheath layer is 6.0 or more.

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