JP2015199795A - Silane-grafted chlorinated polyethylene and method for producing the same, and insulated wire and cable - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a silane-grafted chlorinated polyethylene obtained by graft-copolymerizing a silane compound having a methacrylic group capable of obtaining a high crosslinking degree when cross-linked.SOLUTION: There is provided a silane-grafted chlorinated polyethylene which is obtained by graft copolymerizing a silane compound having a methacrylic group represented by HC=C(CH)-CO- to a chlorinated polyethylene with a peroxide, wherein when the molar number of the silane compound is defined as x, the molar number of the peroxide is defined as y and the number of oxygen-oxygen bonds contained in the peroxide is defined as α, x/2αy is 1.5 or more and 20.0 or less and the gel fraction after crosslinking is 60% or more.

Description

  The present invention relates to a silane-grafted chlorinated polyethylene, a method for producing the same, an insulated wire and a cable.

  Chlorinated polyethylene is a kind of thermoplastic elastomer obtained by reacting polyethylene as a raw material with chlorine by a method such as an aqueous suspension method. Chlorinated polyethylene has a wide range of properties such as flexibility, weather resistance, oil resistance, chemical resistance, flame resistance, heat resistance, and wear resistance. Is widely used as a material for forming.

  Generally, when a sheath is formed of chlorinated polyethylene, it is known to crosslink the chlorinated polyethylene after the chlorinated polyethylene is extruded. As a crosslinking method, silane crosslinking using a silane compound (silane coupling agent) is widely performed (see, for example, Patent Document 1).

  In silane crosslinking, first, a silane compound and a peroxide are contained in chlorinated polyethylene, and the silane compound is graft copolymerized with the chlorinated polyethylene in the presence of the peroxide to form a silane-grafted chlorinated polyethylene. Next, silane-crosslinked chlorinated polyethylene is formed by bringing the silane-grafted chlorinated polyethylene into contact with water and crosslinking.

  As the silane compound, for example, a silane compound having a vinyl group such as vinyltrimethoxysilane or vinyltriethoxysilane (hereinafter also referred to as vinylsilane) is widely used. However, vinyl silane has a problem that it is difficult to handle because it is highly volatile and has a unique irritating odor. Therefore, a silane compound having a methacryl group, an acryl group or a styryl group has been studied as a silane compound instead of vinyl silane. Of these, silane compounds having a methacryl group (hereinafter also referred to as methacryl silane) have attracted attention because of their high practicality in terms of cost and the like.

Japanese Patent No. 50-35540

  However, methacryl silane is less likely to be graft copolymerized with chlorinated polyethylene than vinyl silane. Therefore, the silane graft chlorinated polyethylene obtained by graft copolymerization of methacryl silane has a problem that the degree of crosslinking is lowered.

  The present invention has been made in view of such problems. A silane-grafted chlorinated polyethylene obtained by graft-copolymerizing a silane compound having a methacryl group, which has a high degree of crosslinking when crosslinked, is obtained. It aims at providing the insulated wire and cable which were used.

According to one aspect of the invention,
A silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO— is graft-copolymerized to a chlorinated polyethylene by a peroxide, wherein the number of moles of the silane compound is x, and the peroxide Where y / 2 is the number of moles of oxygen and α is the number of bonds between oxygen and oxygen contained in the peroxide, x / 2αy is 1.5 or more and 20.0 or less, and the gel fraction after crosslinking A silane-grafted chlorinated polyethylene is provided in which is 60% or more.

According to another aspect of the invention,
Adding the peroxide to the chlorinated polyethylene, and adding the silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO— to the chlorinated polyethylene, the chlorination A grafting step of graft-copolymerizing the silane compound onto polyethylene, wherein in the grafting step, the number of moles of the silane compound is x, the number of moles of the peroxide is y, and oxygen contained in the peroxide When the number of bonds between oxygen and oxygen is α, the silane compound is added so that x / 2αy is 1.5 or more and 20.0 or less, and the grafting step is performed after the addition step. A method for producing silane-grafted chlorinated polyethylene is provided.

According to yet another aspect of the invention,
A silane compound having a methacrylic group represented by H ₂ C═C (CH ₃ ) —CO—, which is provided so as to surround the conductor and the outer periphery of the conductor, is graft-copolymerized to the chlorinated polyethylene by a peroxide. Where x / 2αy is 1.5 or more, where x is the number of moles of the silane compound, y is the number of moles of the peroxide, and α is the number of bonds between oxygen and oxygen contained in the peroxide. And an insulating layer formed of silane-grafted chlorinated polyethylene having a gel fraction of 60% or more.

According to yet another aspect of the invention,
Silane compound having a methacryl group, H ₂ C═C (CH ₃ ) —CO—, which is provided so as to surround the conductor, an insulating layer provided so as to surround the outer periphery of the conductor, and an outer periphery of the insulating layer Is graft-copolymerized to chlorinated polyethylene by peroxide, the number of moles of the silane compound is x, the number of moles of the peroxide is y, and the number of bonds between oxygen and oxygen contained in the peroxide And a jacket layer formed of a silane-grafted chlorinated polyethylene having x / 2αy of 1.5 or more and 20.0 or less, and having a gel fraction of 60% or more. .

  According to the present invention, a silane-grafted chlorinated polyethylene obtained by graft copolymerization with a silane compound having a methacryl group, which can obtain a high degree of crosslinking when crosslinked, an insulated wire and a cable using the silane-grafted chlorinated polyethylene are obtained.

It is sectional drawing of the cable which concerns on one Embodiment of this invention. It is sectional drawing of the insulated wire which concerns on one Embodiment of this invention. It is a schematic diagram which shows the grafting process using the extruder in an Example. It is a schematic diagram which shows preparation of the cable in an Example.

  When the present inventors examined the above-mentioned problems, methacryl silane is less likely to be graft copolymerized with chlorinated polyethylene than vinyl silane, that is, the grafting rate of methacryl silane to chlorinated polyethylene is low. It was found that methacryl silane easily reacts with radicals generated during graft copolymerization. This point will be specifically described below.

  In general, graft copolymerization of a silane compound proceeds by radicals. Specifically, first, a silane compound and a peroxide are contained in chlorinated polyethylene and heated, and the peroxide is thermally decomposed to generate a radical (for example, an oxy radical). Oxy radicals generate chlorinated polyethylene radicals by extracting hydrogen from chlorinated polyethylene. Then, the radical of chlorinated polyethylene and the unsaturated bond (for example, vinyl group or methacryl group) possessed by the silane compound react, whereby the silane compound is graft-copolymerized to chlorinated polyethylene. Thus, the graft copolymerization of the silane compound begins to react with oxy radicals generated from the peroxide.

  However, in the graft copolymerization described above, an oxy radical that reacts with chlorinated polyethylene may react with a silane compound. That is, oxy radicals may be consumed by reaction with the silane compound. Therefore, the reaction between the oxy radical and the chlorinated polyethylene is inhibited, and the radical of the chlorinated polyethylene is hardly generated. As a result, the silane compound is not sufficiently graft copolymerized with the chlorinated polyethylene, and the grafting rate of the silane compound becomes low. In particular, among silane compounds, methacrylic silane has a higher reactivity with oxy radicals and easily reacts with oxy radicals than vinyl silane and the like, so that the grafting rate becomes lower. Thus, when the grafting rate of a silane compound becomes low, when a silane graft | grafting chlorinated polyethylene is bridge | crosslinked, a crosslinking degree will become low.

  When the present inventors examined a method for solving this problem, it is preferable not to add methacrylic silane at the same time as the peroxide, but to add methacrylic silane after adding the peroxide to chlorinated polyethylene. It was found. Conventionally, when a peroxide and a silane compound are added to chlorinated polyethylene, for example, a solution in which the peroxide and the silane compound are dissolved is added at the same time. However, in the case of methacrylic silane, when added simultaneously with the peroxide, the radicals generated from the peroxide react with the methacrylic silane while they are dispersed in the chlorinated polyethylene. As a result, the graft copolymerization of methacrylsilane is hindered. On the other hand, when methacrylsilane is added after adding the peroxide, the peroxide can be dispersed in the chlorinated polyethylene in advance, so that the consumption of the peroxide is increased when methacrylsilane is dispersed. Can be suppressed. As a result, methacryl silane can be satisfactorily graft copolymerized with chlorinated polyethylene. The present invention has been made based on these findings.

<One Embodiment of the Present Invention>
Hereinafter, an embodiment of the present invention will be described.

(1) Silane-grafted chlorinated polyethylene The silane-grafted chlorinated polyethylene of this embodiment is obtained by graft-copolymerizing a silane compound having a methacrylic group (methacrylic silane) to chlorinated polyethylene with a peroxide. Silane-grafted chlorinated polyethylene has a silane group derived from a silane compound in the molecular chain and has a structure that is crosslinked by reaction with water. Hereinafter, each component will be specifically described.

  The chlorinated polyethylene can be obtained, for example, by blowing chlorine gas into an aqueous suspension obtained by suspending and dispersing linear polyethylene (such as low density polyethylene or high density polyethylene) in water. The degree of chlorination of the chlorinated polyethylene is preferably 25% or more and 45% or less, and 30% or more and 40% or less from the viewpoint of improving the grafting rate of the silane compound, that is, improving the degree of crosslinking when crosslinked. Then better.

The silane compound has a methacryl group represented by H ₂ C═C (CH ₃ ) —CO—. The methacryl group is an unsaturated bond substituent that reacts with the radicals of chlorinated polyethylene. The silane compound is graft-copolymerized to chlorinated polyethylene by the reaction of the methacrylic group with the radical of chlorinated polyethylene.

  Moreover, the silane compound has a hydrolyzable silane group. In the chemical structure of silane-grafted chlorinated polyethylene, a silane group is introduced by graft copolymerization of the silane compound with chlorinated polyethylene. The silane group is converted to a silanol group by hydrolysis when the silane-grafted chlorinated polyethylene is reacted with water for crosslinking. Silanol groups form a crosslinked structure by dehydration condensation (silanol condensation). Examples of the silane group include those having a hydrolyzable structure such as a halogen, an alkoxy group, an acyloxy group, and a phenoxy group. Examples of the silane group having a hydrolyzable structure include a halosilyl group, an alkoxysilyl group, an acyloxysilyl group, and a phenoxysilyl group.

  Specifically, as the silane compound, methacryl silane such as 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropyltriethoxysilane, 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, etc. Can be used.

  The peroxide is for graft copolymerizing a silane compound with chlorinated polyethylene. Peroxides are organic peroxides that have high hydrogen abstraction ability to extract hydrogen from chlorinated polyethylene, and can generate oxy radicals by thermal decomposition at a temperature at which chlorinated polyethylene is unlikely to deteriorate (hard to dehydrochlorinate). Can be used. Since the deterioration start temperature of chlorinated polyethylene is about 200 ° C., it is preferable to use an organic peroxide having a one-minute half-life temperature of 120 ° C. or more and 200 ° C. or less as the peroxide. From the viewpoint of shortening the time required for the grafting reaction, it is better to use an organic peroxide having a one-minute half-life temperature of 150 ° C. or higher and 200 ° C. or lower. The 1-minute half-life temperature is a temperature at which the half-life of the peroxide is 1 minute.

  Specifically, as the peroxide, bis (1-methyl-1-phenylethyl) peroxide (dicumyl peroxide), 1,1-di (t-butylperoxy) cyclohexane, t-butylperoxyisopropyl Carbonate, t-amyl peroxyisopropyl carbonate, 2,5 dimethyl 2,5 di (t-butylperoxy) cyclohexane, t-butylperoxy 2-ethylhexyl carbonate, and the like can be used. These may be used alone or in combination of two or more. Among these, bis (1-methyl-1-phenylethyl) peroxide (so-called dicumyl peroxide) having a 1 minute half-life temperature of about 175 ° C. may be used.

  The number of moles of the silane compound is x, the number of moles of the peroxide is y, and the number of oxygen-oxygen bonds (peroxide bond, —O—O— bond) contained in the peroxide. Where x / 2αy is preferably 1.5 or more and 20.0 or less, and more preferably 3 or more and 9 or less. x / 2αy represents the ratio between the number of moles of the silane compound blended in the chlorinated polyethylene and the number of moles of radicals (oxy radicals) generated from the peroxide. When x / 2αy is less than 1.5, radicals tend to be insufficient with respect to the silane compound, so that there is a possibility that the silane compound cannot be sufficiently copolymerized with chlorinated polyethylene. On the other hand, if x / 2αy exceeds 20.0, radicals tend to be excessive with respect to the silane compound, and thus an unintended crosslinking reaction may occur when the silane compound is graft-copolymerized. Therefore, when x / 2αy is 1.5 or more and 20 or less, the silane compound can be sufficiently graft copolymerized with chlorinated polyethylene, and the crosslinking reaction when graft copolymerization can be suppressed.

The silane compound and the peroxide are not particularly limited as long as the content is such that x / 2αy is 1.5 or more and 20.0 or less. For example, the content of the silane compound is preferably 1.0 part by mass or more and 10 parts by mass or less with respect to 100 parts by mass of chlorinated polyethylene. The peroxide content is preferably 0.03 parts by mass or more and 3.0 parts by mass or less. At this time, the number of moles x of the silane compound is preferably in the range of 4.0 × 10 ⁻³ to 4.0 × 10 ⁻² , and the number of moles 2αy of radicals (oxy radicals) generated from the peroxide is 2. It is good in the range of ² * 10 ^{< -4} > -2.2 * 10 ^<-2 >.

  The silane-grafted chlorinated polyethylene preferably contains a silanol condensation catalyst that promotes the crosslinking reaction from the viewpoint of efficient crosslinking. As the silanol condensation catalyst, for example, a group II element such as magnesium and calcium, a group VIII element such as cobalt and iron, a metal element such as tin, zinc and titanium, and a metal compound containing these elements can be used. In addition, metal salts of octylic acid and adipic acid, amine compounds, acids, and the like can be used. Specifically, dioctyltin dineodecanoate, dibutyltin dilaurate, dibutyltin diacetate, dibutyltin dioctaate, stannous acetate, stannous carbrate, lead naphthenate, zinc caprylate, cobalt naphthenate, etc. Metal salts, amine compounds such as ethylamine, dibutylamine, hexylamine and pyridine, inorganic acids such as sulfuric acid and hydrochloric acid, and organic acids such as toluenesulfonic acid, acetic acid, stearic acid and maleic acid can be used.

  Silane-grafted chlorinated polyethylene includes plasticizers, antioxidants (including antioxidants), fillers such as carbon black, flame retardants, lubricants, copper damage discoloration inhibitors, crosslinking aids, stabilizers, etc. Other additives may be contained.

(2) Silane-crosslinked chlorinated polyethylene Silane-crosslinked chlorinated polyethylene is obtained by crosslinking the above-mentioned silane-grafted chlorinated polyethylene by reaction with water. Silane-crosslinked chlorinated polyethylene has a gel fraction, which is an index of the degree of crosslinking, for example, of 60% or more. When the gel fraction is less than 60%, the degree of cross-linking of the silane-crosslinked chlorinated polyethylene is low, and therefore mechanical properties such as tensile strength cannot be obtained in the jacket layer (sheath) provided in the cable. From the viewpoint of improving mechanical properties such as a sheath, the upper limit of the gel fraction is not particularly limited. As the gel fraction increases and the degree of cross-linking increases, many cross-linked structures are formed in the silane cross-linked chlorinated polyethylene, and therefore, mechanical properties such as a sheath tend to be improved.

The gel fraction is determined as follows. First, a sample formed of silane-crosslinked chlorinated polyethylene is immersed in xylene, and xylene is heated and boiled. Thereafter, a sample that remains without being dissolved in xylene (sample after extraction with hot xylene) is taken out and dried, and the mass of the sample after extraction with hot xylene is measured. Then, by calculating the ratio of the mass of the sample after extraction with hot xylene to the mass of the sample before extraction with hot xylene, the gel fraction of the silane-crosslinked chlorinated polyethylene is determined. When the mass of the sample before extraction with hot xylene is a, and the mass of the sample after extraction with hot xylene is b, the gel fraction R is expressed by the following formula.
R (%) = (b / a) × 100

(3) Manufacturing method of silane graft chlorinated polyethylene Next, the manufacturing method of the silane graft chlorinated polyethylene mentioned above is demonstrated.

(Addition process)
First, for example, dicumyl peroxide is added as a peroxide to chlorinated polyethylene and heated and kneaded. By kneading, the peroxide is dispersed in the chlorinated polyethylene. At this time, a peroxide is added in an amount of 0.03 to 3.0 parts by mass, preferably 0.1 to 1.2 parts by mass, with respect to 100 parts by mass of chlorinated polyethylene. In addition, the temperature at the time of kneading | mixing is good to be below the deterioration temperature of chlorinated polyethylene.

(Grafting process)
Subsequently, methacrylic silane having a methacrylic group is added to chlorinated polyethylene in which the peroxide is dispersed, followed by heating and kneading. Methacrylsilane is dispersed in chlorinated polyethylene by kneading. In the grafting step, x / 2αy is 1.5 or more and 20 when the number of moles of the silane compound is x, the number of moles of peroxide is y, and the number of bonds between oxygen and oxygen contained in the peroxide is α. It is good to add methacryl silane so that it may become 0.0 or less. For example, 1.0 to 10 parts by mass of methacrylic silane may be added to 100 parts by mass of chlorinated polyethylene.

  By adding methacrylic silane to chlorinated polyethylene, methacrylic silane is graft copolymerized with chlorinated polyethylene in the presence of peroxide to form silane-grafted chlorinated polyethylene. In this embodiment, by adding a peroxide to chlorinated polyethylene and dispersing it in advance, when methacrylic silane is dispersed in chlorinated polyethylene, the reaction between oxy radicals generated from the peroxide and methacrylic silane is suppressed. can do. That is, the oxy radical produced | generated from a peroxide can be made to react efficiently with chlorinated polyethylene, and the radical of chlorinated polyethylene can be produced | generated efficiently. Thereby, even if it is a case where methacryl silane with high reactivity with an oxy radical is used, it can be made to graft-polymerize suitably to chlorinated polyethylene.

  In the above-described addition step and grafting step, kneading may be performed using a kneading reaction apparatus such as a roll machine, an extruder, a kneader, a mixer, or an autoclave. Further, kneading conditions and graft reaction conditions (temperature, time, etc.) are not particularly limited.

(4) Cable Configuration and Manufacturing Method Next, the cable 1 according to an embodiment of the present invention will be described. FIG. 1 is a cross-sectional view of a cable 1 according to an embodiment of the present invention.

  As shown in FIG. 1, the cable 1 of this embodiment includes a conductor 10. As the conductor 10, a copper wire made of low-oxygen copper, oxygen-free copper, or the like, a copper alloy wire, a metal wire made of aluminum, silver, or the like, or a stranded wire formed by twisting metal wires can be used. The outer diameter of the conductor 10 can be appropriately changed according to the use of the cable 1.

  An insulating layer 11 is provided so as to cover the outer periphery of the conductor 10. The insulating layer 11 is formed of a conventionally known resin composition, for example, a resin composition containing ethylene propylene rubber. The thickness of the insulating layer 11 can be appropriately changed according to the use of the cable 1.

  An outer cover layer 12 (sheath 12) is provided so as to cover the outer periphery of the insulating layer 11. The sheath 12 is formed of silane-crosslinked chlorinated polyethylene obtained by crosslinking silane-grafted chlorinated polyethylene. The sheath 12 is made of silane-crosslinked chlorinated polyethylene having a gel fraction of 60% or more, and has a high degree of crosslinking.

  The cable 1 is manufactured as follows, for example. First, for example, a copper wire is prepared as the conductor 10. Then, for example, an extruder is used to extrude the resin composition containing ethylene propylene rubber so as to cover the outer periphery of the conductor 10 to form the insulating layer 11 having a predetermined thickness. Subsequently, the sheath 12 is formed by extruding the above-mentioned silane-grafted chlorinated polyethylene with a predetermined thickness so as to cover the outer periphery of the insulating layer 11. Thereafter, the silane-grafted chlorinated polyethylene that forms the sheath 12 is reacted with water to form a silane-crosslinked chlorinated polyethylene, thereby cross-linking the sheath 12. Specifically, in the silane-grafted chlorinated polyethylene forming the sheath 12, the silane group in the chemical structure is hydrolyzed into a silanol group by reaction with water. Then, silanol groups are dehydrated and condensed to bond with each other so that the molecular chain of the silane-grafted chlorinated polyethylene is crosslinked to form a silane-crosslinked chlorinated polyethylene. Thereby, the sheath 12 is bridge | crosslinked and the cable 1 of this embodiment is obtained. In addition, when bridge | crosslinking a silane graft | grafting chlorinated polyethylene, it is good to carry out in 60 degreeC saturated water vapor | steam atmosphere, for example.

<Effects of Embodiment of the Present Invention>
According to the present embodiment, the following one or more effects are achieved.

(A) According to the present embodiment, the grafting step is performed after the peroxide addition step. That is, by adding a peroxide to chlorinated polyethylene and then adding methacrylic silane, the silane compound is graft-copolymerized to chlorinated polyethylene to form a silane-grafted chlorinated polyethylene. When methacrylic silane is dispersed in chlorinated polyethylene and graft copolymerized, the peroxide is added to the chlorinated polyethylene and dispersed in advance, so the reaction between the oxy radicals generated from the peroxide and methacrylic silane Can be suppressed. That is, oxy radicals can be reacted with chlorinated polyethylene to generate chlorinated polyethylene radicals efficiently. Thereby, methacryl silane can be suitably graft copolymerized with chlorinated polyethylene, and the grafting rate of methacryl silane in the silane-grafted chlorinated polyethylene can be improved. Therefore, when the silane-grafted chlorinated polyethylene is crosslinked, a silane-crosslinked chlorinated polyethylene having a gel fraction of 60% or more and a high degree of crosslinking can be obtained.

  On the other hand, when methacryl silane is added to chlorinated polyethylene at the same time as the peroxide as in the past, oxy radicals generated from the peroxide react with methacryl silane when these are dispersed in chlorinated polyethylene. As a result, peroxide is consumed. Therefore, methacrylsilane cannot be efficiently graft copolymerized with chlorinated polyethylene. As a result, the grafting rate of methacrylic silane is reduced, and the gel fraction when the silane-grafted chlorinated polyethylene is crosslinked is less than 60%.

(B) According to this embodiment, when methacrylic silane is dispersed in chlorinated polyethylene and graft copolymerized, the peroxide is added to the chlorinated polyethylene and dispersed in advance. Therefore, radicals can be uniformly generated in the chlorinated polyethylene from the dispersed peroxide. Then, by uniformly dispersing methacryl silane in chlorinated polyethylene, methacryl silane can be uniformly graft-copolymerized into the chemical structure of chlorinated polyethylene, and silane groups can be introduced uniformly. As a result, the chlorinated polyethylene can be uniformly crosslinked, so that variation in the degree of crosslinking of the silane-crosslinked chlorinated polyethylene (local crosslinking) can be reduced and mechanical properties such as elongation can be improved. In addition, it is possible to reduce appearance defects due to the protrusions caused by the chlorinated polyethylene being locally crosslinked excessively.

(C) According to this embodiment, when the number of moles of the silane compound is x, the number of moles of peroxide is y, and the number of bonds between oxygen and oxygen contained in the peroxide is α / 2αy Is 1.5 or more and 20.0 or less. When x / 2αy is 1.5 or more, methacrylic silane can be efficiently graft copolymerized with chlorinated polyethylene by supplying radicals sufficiently to methacrylic silane without being insufficient. When x / 2αy is 20.0 or less, the chlorinated polyethylene undergoes a crosslinking reaction when graft copolymerizing methacrylic silane by supplying radicals so as not to be excessive with respect to methacrylic silane. Can be suppressed. Therefore, when x / 2αy is 1.5 or more and 20 or less, the silane compound can be sufficiently graft copolymerized with chlorinated polyethylene, and the crosslinking reaction when graft copolymerization can be suppressed.

(D) According to the present embodiment, by using methacryl silane instead of vinyl silane having high volatility and an irritating odor, the work environment can be improved and the grafting process can be performed stably. it can. In addition, since methacrylic silane has a higher boiling point and flash point than vinyl silane, it is possible to suppress the occurrence of a fire in a manufacturing process such as a grafting process.

(E) According to the present embodiment, the sheath of the cable is formed of silane-crosslinked chlorinated polyethylene having a gel fraction of 60% or more obtained by crosslinking silane-grafted chlorinated polyethylene. Therefore, the cable has a high mechanical strength.

<Other Embodiments of the Present Invention>
As mentioned above, although one Embodiment of this invention was described concretely, this invention is not limited to the above-mentioned embodiment, In the range which does not deviate from the summary, it can change suitably.

  In the above-described embodiment, the case where the silane-grafted chlorinated polyethylene is used for the jacket layer 12 (sheath 12) of the cable 1 has been described. However, the present invention is not limited to this. Silane graft chlorinated polyethylene can also be used for the insulating layer 11 of the insulated wire 2 as shown in FIG. 2, for example. In this case, as in the case of forming the sheath 12 in the above-described embodiment, the insulating layer 11 is formed by extruding the silane-grafted chlorinated polyethylene to the outer periphery of the conductor 10, and the insulating layer 11 is brought into contact with water for silane crosslinking. Good.

  Next, examples of the present invention will be described.

  The materials used in Examples and Comparative Examples are as follows.

Chlorinated polyethylene (Mooney viscosity at 121 ° C. (ML1 + 4): 55, heat of fusion: less than 1.0 J / g): “CM352L” manufactured by Hangzhou Science & Technology Co., Ltd.
-Hydrotalcite: “Mugcellar 1” manufactured by Kyowa Chemical Industry Co., Ltd.
Epoxidized soybean oil: “New Sizer 510R” manufactured by Nippon Oil & Fats Co., Ltd.
Polyethylene wax (PE wax, molecular weight: 2800): “High Wax NL-200” manufactured by Mitsui Chemicals, Inc.
・ Peroxide (Dicumyl peroxide): “DCP” manufactured by NOF Corporation
Silane compound (3-methacryloxypropyltrimethoxysilane): “KBM-503” manufactured by Shin-Etsu Chemical Co., Ltd.
Silane compound (3-methacryloxypropyltriethoxysilane): “KBE-503” manufactured by Shin-Etsu Chemical Co., Ltd.
・ Plasticizer (naphthenic process oil): “NP-24” manufactured by Idemitsu Kosan Co., Ltd.
・ Sulfur-based antioxidant (4,4′-thiobis (3-methyl-6-tert-butylphenol)): “NOCRACK 300R” manufactured by Ouchi Shinsei Chemical Co., Ltd.
Amine-based antioxidant (2,2,4-trimethyl-1,2-dihydroquinoline polymer): “NOCRACK 224” manufactured by Ouchi Shinsei Chemical Co., Ltd.
・ Flame retardant (antimony trioxide): “Antimony trioxide” manufactured by Sumitomo Metal Mining Co., Ltd.
・ Carbon (FEF carbon black): “Asahi Carbon 60G” manufactured by Asahi Carbon Co., Ltd.
・ Lubricant (ethylenebisoleic acid amide): “Sripac-O” manufactured by Nippon Kasei Co., Ltd.
Silanol condensation catalyst (dioctyltin dineodecanoate): “Neostan U-830” manufactured by Nitto Kasei Co., Ltd.

(1) Preparation of chlorinated polyethylene composition (Example 1)
In this example, a peroxide addition step, a grafting step, and a filler addition step were sequentially performed to prepare a chlorinated polyethylene composition containing a silane-grafted chlorinated polyethylene.

[Peroxide addition process]
First, using an 8-inch roll machine, 6 parts by mass of hydrotalcite as a stabilizer and 2 parts by mass of epoxidized soybean oil as a stabilizer with respect to 100 parts by mass of powdered chlorinated polyethylene, 3 parts by mass of polyethylene wax as a lubricant was added and kneaded to prepare Compound A. To this compound A, dicumyl peroxide as a peroxide was added and kneaded so as to be 0.1 parts by mass with respect to 100 parts by mass of chlorinated polyethylene. Thereafter, a sheet made of the mixture obtained by kneading was pelletized into a 5 mm square shape to obtain pellets. And in order to prevent adhesion between these pellets, talc was applied to the pellets. When the peroxide was kneaded, the peroxide was sufficiently dispersed in the chlorinated polyethylene and the peroxide was not thermally decomposed. Specifically, the surface temperature of the roll was set to 100 ° C. and kneading was performed for 5 minutes after adding the peroxide.

[Grafting process]
Then, using the single screw extruder 100 shown in FIG. 3, the pellet obtained by the addition process was impregnated with the silane compound, and the graft process was performed. Specifically, the pellet obtained in the addition step was impregnated with 3-methacryloxypropyltrimethoxysilane as a silane compound so as to be 3.35 parts by mass with respect to 100 parts by mass of chlorinated polyethylene. The pellet impregnated with the silane compound was put into the cylinder 103 a from the hopper 101 of the single screw extruder 100, and sent out from the cylinder 103 a to the cylinder 103 b by the rotation of the screw 102. At this time, the pellets were heated and softened and kneaded by the cylinders 103a and 103b to graft copolymerize the chlorinated polyethylene with the silane compound. This formed the silane graft | grafting chlorinated polyethylene. Thereafter, the silane-grafted chlorinated polyethylene was fed to the head portion 104 of the extruder 100, and a strand 20 (length: 150 cm) of the silane-grafted chlorinated polyethylene was extruded from the die 105. Then, the strand 20 was introduced into the water tank 106, cooled with water, and drained with an air wiper 107. Thereafter, the strand 20 was pelletized with a pelletizer 108 to obtain pellets 21 containing silane-grafted chlorinated polyethylene.
In the grafting process, a 40 mm single screw single screw extruder 100 was used. The ratio L / D between the screw diameter D and the screw length L was 25. Further, the temperature of the cylinder 103a was 80 ° C., the temperature of the cylinder 103b was 200 ° C., and the temperature of the head portion 104 was 200 ° C. Moreover, the rotation speed of the screw 102 was 20 rpm, and the screw 102 was made into the full flight shape. Further, a die having a hole diameter of 5 mm and three holes was used as the die 105.

[Filler addition process]
Subsequently, various fillers were added to the pellets 21 obtained in the grafting step and kneaded using an 8-inch roll machine. Specifically, 10 parts by mass of a naphthenic process oil as a plasticizer, 0.08 parts by mass of a sulfur-based antioxidant, and 1.5 parts by mass of an amine-based antioxidant with respect to 100 parts by mass of chlorinated polyethylene. Various additives were added so that 3 parts by mass of antimony trioxide as a flame retardant, 40 parts by mass of FEF carbon black as carbon black, and 1 part by mass of ethylenebisoleic acid amide as a lubricant were added. After kneading, a sheet made of the kneaded material was pelletized into a 5 mm square shape to obtain Compound B pellets. During kneading, the surface temperature of the roll was set to 100 ° C., and all the fillers were added and kneaded for 5 minutes.

  In addition to the compound B pellets, a silanol condensation catalyst master batch containing a silanol condensation catalyst was prepared. Specifically, 1 part by mass of dioctyltin dineodecanoate as a silanol condensation catalyst was added to 111 parts by mass of compound A and kneaded using an 8-inch roll machine. At this time, the surface temperature of the roll was set to 100 ° C., and the kneading was carried out for 3 minutes after the silanol condensation catalyst was added. Then, the sheet | seat which consists of kneaded materials was pelletized in the shape of 5 square mm, and the silanol condensation catalyst masterbatch was prepared.

  Finally, the silanol condensation catalyst master batch is added to the pellets of compound B so as to be 2.5 parts by mass with respect to 100 parts by mass of chlorinated polyethylene of compound B, and dry blending is performed. A polyethylene composition was prepared.

  The preparation conditions of Example 1 are shown in Table 1 below.

(Example 2)
In Example 2, as shown in Table 1, the type of the silane compound was changed to 3-methacryloxypropyltriethoxysilane, and the addition amount was 3.92 parts by mass with respect to 100 parts by mass of chlorinated polyethylene. Prepared a chlorinated polyethylene composition in the same manner as in Example 1.

(Examples 3 and 4)
In Examples 3 and 4, as shown in Table 1, except that the amount of peroxide added was increased and the ratio (x / 2αy) between the silane compound and radicals generated from the peroxide was changed. A chlorinated polyethylene composition was prepared in the same manner as in Example 1. In Example 3, the amount of peroxide added was 0.5 parts by mass, and the ratio was 3.7. In Example 4, the amount of peroxide added was 1.0 part by mass, and the ratio was 1.8.

(Comparative Example 1)
In Comparative Example 1, as shown in Table 1, a chlorinated polyethylene composition was prepared in the same manner as in Example 1 except that Compound A pellets were impregnated with a peroxide and a silane compound at the same time.

(Comparative Examples 2 to 4)
In Comparative Examples 2 to 4, as shown in Table 1, chlorinated polyethylene compositions were prepared in the same manner as in Example 1 except that the peroxide content was changed. The peroxide content was 0.02 parts by mass in Comparative Example 2, 0.08 parts by mass in Comparative Example 3, and 1.5 parts by mass in Comparative Example 4.

(2) Production of cable Next, the cable 1 was produced by extruding the prepared chlorinated polyethylene composition with the single screw extruder 100 shown in FIG. Specifically, a copper conductor having a cross-sectional area of 8 mm ² is inserted as the conductor 10 into the die 105 of the single-screw extruder 100, and ethylene propylene rubber (EP rubber) is extruded on the outer periphery thereof to have a thickness of 1.0 mm. The cable 1 was produced by forming the insulating layer 11 and extruding the above-described chlorinated polyethylene composition on the outer periphery of the insulating layer 11 to form a sheath 12 having a thickness of 1.7 mm. Thereafter, the cable 1 was stored for 24 hours in a sealed stainless steel container having a saturated water vapor atmosphere at 60 ° C. to crosslink the sheath 12.
In manufacturing the cable 1, a 20 mm single-screw single-screw extruder 100 was used. The ratio L / D between the screw diameter D and the screw length L was 15. The temperature of the cylinder 103a was 120 ° C., the temperature of the cylinder 103b was 150 ° C., the temperature of the crosshead portion 110 was 150 ° C., the temperature of the neck 109 was 150 ° C., and the temperature of the die 105 was 150 ° C. Moreover, the rotation speed of the screw 102 was 15 rpm, and the shape of the screw 102 was a full flight shape.

(3) Evaluation method About the chlorinated polyethylene composition, the gel fraction after a grafting process and the gel fraction after a crosslinking process were evaluated. Further, the appearance of the cable 1 was evaluated. This will be specifically described below.

(Gel fraction)
In this example, a silane-grafted chlorinated polyethylene strand 20 was used as a sample in order to evaluate the gel fraction after the grafting step. A 0.5 g sample was taken from the strand 20, and the sample was placed in a 40 mesh brass wire mesh. Subsequently, the sample was extracted with xylene in a 110 ° C. oil bath. After the extraction treatment, the remaining sample was taken out from xylene and vacuum-dried at 80 ° C. for 4 hours. Then, the mass of the remaining sample after drying was weighed, and the gel fraction R of the sample was calculated from the following equation using the mass a of the sample before xylene extraction and the mass b of the remaining sample after xylene extraction.
R (%) = b / a × 100

  Further, in order to evaluate the gel fraction after the crosslinking treatment, 0.5 g of a sample was taken from the sheath 12 of the cable 1 and the gel fraction was calculated in the same manner as described above. In this example, the case where the gel fraction after the crosslinking treatment was 60% or more was determined to be acceptable (◯), and the case where the gel fraction was less than 60% was determined to be unacceptable (x).

(appearance)
Appearance is evaluated by visually and touching the outer appearance of the sheath 12 of the cable 1, and when it is sufficiently smooth, it is accepted (O), and the outer appearance is poor due to roughness or protrusions (local protrusions) on the sheath 12. The case where it was was made into the failure (x).

(Comprehensive evaluation)
In the present Example, the case where it passed by evaluation of both a gel fraction and an external appearance was set as the pass ((circle)), and the case where any one failed was set as the disqualification (x).

(4) Evaluation results In Example 1, as shown in Table 1, it was confirmed that the gel fraction of the strand after the grafting process was 2%, and the unintended crosslinking reaction did not proceed excessively in the grafting process. It was. Moreover, in the sheath 12 of Example 1, it was confirmed that the gel fraction after being crosslinked is as high as 67% and has a sufficient degree of crosslinking. Further, it was confirmed that the appearance of the sheath 12 was smooth and good. In Example 1, since methacrylic silane having less volatility and less irritating odor was used compared to vinyl silane, there was no problem that the working environment deteriorated when preparing a chlorinated polyethylene composition. It was.

  In Example 2, as shown in Table 1, even when the type of methacrylsilane was changed, it was confirmed that the gel fraction and the appearance were evaluated well as in Example 1.

  In Examples 3 and 4, as shown in Table 1, it was confirmed that the gel fraction after crosslinking can be improved as the amount of peroxide added is increased and the ratio (x / 2αy) is decreased. . In Examples 3 and 4, since the ratio (x / 2αy) was decreased to increase the radical ratio, it was confirmed that the gel fraction after the grafting step was higher than that in Example 1.

  In Comparative Example 1, since methacrylsilane was added simultaneously with the peroxide, it was confirmed that the gel fraction after crosslinking was 58%. This is probably because methacrylsilane was added at the same time as the peroxide, and radicals generated from the peroxide were consumed by the methacrylsilane, and the methacrylsilane could not be efficiently graft copolymerized.

  In Comparative Examples 2 and 3, since the amount of peroxide added is too small relative to methacrylic silane, the gel fraction after crosslinking is 30% and 34%, respectively, and a sufficient degree of crosslinking cannot be obtained. Was confirmed. In Comparative Examples 2 and 3, since the amount of peroxide added was small, the gel fraction after the grafting process was 0%, and it was confirmed that an unintended crosslinking reaction did not proceed in the grafting process.

  In Comparative Example 4, since the amount of peroxide added was too large relative to methacrylic silane, the crosslinking reaction proceeded during the grafting process, and it was confirmed that the gel fraction after the grafting process was as high as 71%. . Further, since the gel fraction after the grafting process was as high as 71%, it was confirmed that when the silane-grafted chlorinated polyethylene was extruded to form a strand, the discharge amount became unstable and the strand was frequently cut. Moreover, the surface of the sheath formed with this chlorinated polyethylene composition was confirmed to have roughness and protrusions (protrusions) that were considered to be caused by local excessive crosslinking reaction. In Comparative Example 4, the gel fraction after crosslinking was 89%, and it was confirmed that the degree of crosslinking was high.

In the present _embodiment has described the case of using a silane compound having a _{H 2 C = C (CH 3} ) -CO- methacryl group represented by _the acrylic group represented by H 2 C = CH-CO- Even if it is the silane compound which has, it is thought that the same effect is acquired.

<Preferred embodiment of the present invention>
Hereinafter, preferred embodiments of the present invention will be additionally described.

[Appendix 1]
According to one aspect of the invention,
A silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO— is graft-copolymerized to a chlorinated polyethylene by a peroxide,
When the number of moles of the silane compound is x, the number of moles of the peroxide is y, and the number of bonds between oxygen and oxygen contained in the peroxide is α, x / 2αy is 1.5 or more and 20. 0 or less,
A silane-grafted chlorinated polyethylene having a gel fraction after crosslinking of 60% or more is provided.

[Appendix 2]
In the silane-grafted chlorinated polyethylene according to Appendix 1, preferably,
The silane compound is 3-methacryloxypropyltrimethoxysilane or 3-methacryloxypropyltriethoxysilane.

[Appendix 3]
According to another aspect of the invention,
An addition step of adding a peroxide to chlorinated polyethylene;
A grafting step of graft copolymerizing the silane compound with the chlorinated polyethylene by adding a silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO— to the chlorinated polyethylene; Have
In the grafting step, x / 2αy is 1 where x is the number of moles of the silane compound, y is the number of moles of the peroxide, and α is the number of bonds between oxygen and oxygen contained in the peroxide. The silane compound is added so as to be 5 or more and 20.0 or less,
Provided is a method for producing a silane-grafted chlorinated polyethylene, wherein the grafting step is performed after the addition step.

[Appendix 4]
According to another aspect of the invention,
Conductors,
A silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO—, which is provided so as to surround the outer periphery of the conductor, is graft-copolymerized to a chlorinated polyethylene by a peroxide, and the silane When x is the number of moles of the compound, y is the number of moles of the peroxide, and α is the number of bonds between oxygen and oxygen contained in the peroxide, x / 2αy is 1.5 or more and 20.0 or less. And an insulating layer formed of silane-grafted chlorinated polyethylene and having a gel fraction of 60% or more.

[Appendix 5]
According to another aspect of the invention,
Conductors,
An insulating layer provided so as to surround the outer periphery of the conductor;
A silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO—, which is provided so as to surround the outer periphery of the insulating layer, is graft-copolymerized to a chlorinated polyethylene by a peroxide, When the number of moles of the silane compound is x, the number of moles of the peroxide is y, and the number of bonds between oxygen and oxygen contained in the peroxide is α, x / 2αy is 1.5 or more and 20.0. There is provided a cable comprising: a jacket layer formed of silane-grafted chlorinated polyethylene which has the following and a gel fraction of 60% or more.

1 Cable 2 Insulated Wire 10 Conductor 11 Insulating Layer 12 Outer Layer (Sheath)

Claims (5)

A silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO— is graft-copolymerized to a chlorinated polyethylene by a peroxide,
When the number of moles of the silane compound is x, the number of moles of the peroxide is y, and the number of bonds between oxygen and oxygen contained in the peroxide is α, x / 2αy is 1.5 or more and 20. 0 or less,
Silane-grafted chlorinated polyethylene having a gel fraction of 60% or more after crosslinking.   The silane-grafted chlorinated polyethylene according to claim 1, wherein the silane compound is 3-methacryloxypropyltrimethoxysilane or 3-methacryloxypropyltriethoxysilane. An addition step of adding a peroxide to chlorinated polyethylene;
A grafting step of graft copolymerizing the silane compound with the chlorinated polyethylene by adding a silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO— to the chlorinated polyethylene; Have
In the grafting step, x / 2αy is 1 where x is the number of moles of the silane compound, y is the number of moles of the peroxide, and α is the number of bonds between oxygen and oxygen contained in the peroxide. The silane compound is added so as to be 5 or more and 20.0 or less,
The manufacturing method of the silane graft | grafting chlorinated polyethylene which performs the said grafting process after performing the said addition process. Conductors,
A silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO—, which is provided so as to surround the outer periphery of the conductor, is graft-copolymerized to a chlorinated polyethylene by a peroxide, and the silane When x is the number of moles of the compound, y is the number of moles of the peroxide, and α is the number of bonds between oxygen and oxygen contained in the peroxide, x / 2αy is 1.5 or more and 20.0 or less. An insulated wire comprising: an insulating layer formed of silane-grafted chlorinated polyethylene and having a gel fraction of 60% or more. Conductors,
An insulating layer provided so as to surround the outer periphery of the conductor;
A silane compound having a methacryl group represented by H ₂ C═C (CH ₃ ) —CO—, which is provided so as to surround the outer periphery of the insulating layer, is graft-copolymerized to a chlorinated polyethylene by a peroxide, When the number of moles of the silane compound is x, the number of moles of the peroxide is y, and the number of bonds between oxygen and oxygen contained in the peroxide is α, x / 2αy is 1.5 or more and 20.0. A jacket comprising: a jacket layer formed of silane-grafted chlorinated polyethylene and having a gel fraction of 60% or more.

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