JP4450760B2 - Joint materials and gaskets - Google Patents

Description

  The present invention relates to a gasket made of the joint material. In particular, when connecting a fire-resistant double-layer pipe composed of an inner pipe and a fire-resistant outer pipe covering the inner pipe, it can be suitably used as a joint material for a fire-resistant double-layer pipe used in the connecting portion.

Fire prevention compartments of building structures are penetrated by water supply / drainage pipes, gas pipes, distribution pipes, etc., especially rigid PVC pipes are widely used for water supply / distribution pipes, and cement mortar at the joints. Water glass, metallic bands, nonflammable inorganic fiber gaskets, and the like are used.
However, in the so-called wet joint method using cement or water glass as the main raw material, the joint material applied to the joint may be cured with time to cause cracks and peeling, and may cause the joint material to fall off. In the dry joint method using a metal joint cover, since the dimensional shape is set in advance, it is difficult to cope with the shape deformation based on the dimensional error of the pipe.
Furthermore, in these joint methods, after the piping work to the building is completed, the work space is limited and the workability is inferior, and in addition to inferior workability, it is also useful for earthquakes, vibration and wetting of buildings, and expansion and contraction of pipes due to temperature changes. I couldn't cope with it enough.

A flexible fire joint rubber joint material made of rubber, expandable graphite, epoxy resin and inorganic filler has been disclosed (for example, see Patent Document 1), and the brittleness and fire resistance, which have been the conventional problems, have been improved. However, there has been a problem that the epoxy resin blended for imparting the function of holding the thermally expandable graphite under high temperature adheres to the inner wall of the kneading apparatus during kneading, and this removal is extremely difficult. In addition, shape retention at high temperatures was not always sufficient. A composition with improved shape retention has already been disclosed (see, for example, Patent Document 2), but moldability and material strength are still insufficient.
JP 2002-181262 A (page 2: claim 1) JP 2001-348487 A (2nd page: claims 1 to 4)

  The present invention, after thermal expansion in the event of a fire, solidifies to prevent smoke blockage and fire spread, keeps its shape in the solidified state and does not lose shape for a long time, thereby preventing fire spread (hereinafter referred to as fireproof performance) It is an object of the present invention to provide a joint material and gasket having the following.

The present invention includes a vulcanizable rubber, thermally expandable graphite, aluminum phosphite, an inorganic filler, a vulcanizing agent and a vulcanization accelerator, and an oxygen index measured according to JIS K7201 is 40 or more. A joint material, 100 parts by mass of vulcanizable rubber, 5 to 100 parts by mass of thermally expandable graphite, 10 to 150 parts by mass of aluminum phosphite, and 10 to 200 parts by mass of inorganic filler The joint material is 0.1 to 10 parts by mass of the vulcanizing agent and 0.1 to 10 parts by mass of the vulcanization accelerator, and the inorganic filler is aluminum hydroxide. Vulcanizable rubbers are butyl rubber and / or ethylene-propylene-diene rubber. Moreover, this invention is a gasket using the joint material.

  The joint material of the present invention and the gasket made of the joint material form a non-flammable fire-resistant layer that is thermally expanded and solidified in the event of a fire. Has performance.

  Examples of vulcanizable rubber used in the present invention include diene rubbers such as natural rubber, isoprene rubber, styrene-butadiene rubber, and chloroprene rubber, and a small amount of double rubber in the main chain such as butyl rubber and ethylene-propylene rubber. For example, ethylene-propylene-diene rubber having a bond introduced therein may be mentioned. In the joint material of the present invention, not only these simple substances but also two or more kinds may be mixed and used in order to improve kneadability, moldability and the like. Among these, use of at least one of chloroprene rubber and ethylene-propylene-diene rubber is preferable because kneadability and moldability are improved.

Thermally expandable graphite is a powder of natural graphite, pyrolytic graphite, etc., treated with an inorganic acid such as sulfuric acid or nitric acid and a strong oxidizing agent such as concentrated nitric acid or permanganate, and maintains a graphite layered structure. Is a crystalline compound. When these are exposed to a temperature of about 200 ° C. or higher, they thermally expand 100 times or more. These natural graphite, pyrolytic graphite and other powders can be used in various types other than deoxidation treatment and further neutralization treatment.
The particle size of the thermally expandable graphite is preferably about 20 to 400 mesh. When the particle size is smaller than 400 mesh, the expansion coefficient of the thermally expandable graphite is small, and the obtained joint material may not be sufficiently thermally expanded in the event of a fire, and when the particle size is larger than 20 mesh, the dispersibility may be deteriorated. Elasticity may decrease.

  The content of the heat-expandable graphite can be appropriately set depending on the type of rubber, the desired expansion ratio, etc., but is not particularly limited, but usually 5 to 100 parts by mass with respect to 100 parts by mass of the base rubber. Is more preferable, and it is 20-80 mass parts more preferably. If the content of the heat-expandable graphite is less than 5 parts by mass, the obtained joint material may not be sufficiently thermally expanded at the time of fire, and if it exceeds 100 parts by mass, the thermal expansion ratio will be increased, but the strength of the obtained joint material will be There is also a tendency for physical properties such as these to decrease.

  In the present invention, it is necessary to use aluminum phosphite as a shape stabilizer for preventing the deformation of the joint material. The average particle size of the aluminum phosphite used in the present invention is preferably 1 to 100 μm as measured by a laser diffraction method from the viewpoint of dispersibility.

  The content of aluminum phosphite can be appropriately set depending on the desired thermal expansion ratio and the like, and is not particularly limited, but is preferably 10 to 150 parts by mass with respect to 100 parts by mass of rubber. If the shape stabilization performance of the joint material obtained when the amount is less than 10 parts by mass exceeds 150 parts by mass, the flexibility of the joint material obtained tends to decrease.

In the present invention, an inorganic filler is used in order to further improve the flame retardancy of the joint material. The inorganic filler is not particularly limited. For example, silica, diatomaceous earth, alumina, zinc oxide, titanium oxide, magnesium oxide, iron oxide, aluminum hydroxide, magnesium hydroxide, zinc borate, calcium carbonate, Magnesium carbonate, zinc carbonate, barium carbonate, hydrotalcite, calcium sulfate, barium sulfate, calcium silicate, talc, clay, mica, bentonite, activated clay, sepiolite, glass fiber, glass beads, aluminum nitride, boron nitride, carbon black And graphite. These may be used alone or in combination of two or more. Among these, aluminum hydroxide and magnesium hydroxide are preferable in that an increase in temperature can be suppressed by an endothermic reaction due to a dehydration reaction during heating. Of these, aluminum hydroxide is particularly preferred.
From the viewpoint of dispersibility, the average particle diameter of these fillers is preferably 1 to 50 μm as measured by a laser diffraction method.
The joint material of the present invention has an oxygen index of 40 or more. If it is less than 40, the flame retardance at the time of a fire is inadequate.

Although content in particular of an inorganic filler is not restrict | limited, 10-200 mass parts is preferable with respect to 100 mass parts of rubber | gum, More preferably, it is 50-100 mass parts. When the amount is less than 10 parts by mass, the effect of improving the flame retardancy tends to be small, and when the amount exceeds 200 parts by mass, the flexibility and strength of the joint material tend to decrease.

  The vulcanizing agent and vulcanization accelerator used in the present invention improve the degree of crosslinking of vulcanizable rubber and improve the strength of the rubber itself. The strength of rubber can be evaluated by hardness.

Although it does not restrict | limit especially as a vulcanizing agent, For example, sulfur type | system | group which consists of sulfur containing compounds, such as sulfur, polysulfide, and sulfur chloride, p-quinone dioxime, pp'-dibenzoyl quinone oxime, etc. Examples thereof include organic peroxides such as oxime, t-butyl hydroperoxide, acetylacetone peroxide, cumene hydroperoxide. It is recommended that the vulcanizing agent be a sulfur type or a combination thereof. Although the usage-amount of these vulcanizing agents is not restrict | limited in particular, 0.1-10 mass parts per 100 mass parts of rubber | gum, Especially 0.5-5 mass parts is preferable.

  In the present invention, a vulcanization accelerator is used for the purpose of promoting the vulcanization treatment. The vulcanization accelerator is not particularly limited, but examples thereof include thiurams such as tetramethylthiuram disulfide, tetrabutylthiuram disulfide, tetramethylthiuram monosulfide, dipentamethylenethiuram tetrasulfide, and 2-mercaptobenzothiazole. And thiazoles such as dibenzothiazole disulfide, dithiocarbamates such as zinc dimethyldithiocarbamate and zinc diethyldithiocarbamate, aldehyde amines such as n-butyraldehyde aniline, N-cyclohexyl-2-benzothiazylsulfenamide, etc. Sulfenamides, guanidines such as diorthotolyl guanidine and diorthonitrile guanidine, thioureas such as thiocarbanilide, diethylthiourea and trimethylthiourea, Compounds such as Hana, and the like. The vulcanization accelerator may be used in combination of not only these simple substances but also two or more kinds. Although the usage-amount of these vulcanization accelerators is not restrict | limited in particular, it is 0.1-10 mass parts per 100 mass parts of base rubbers, and 0.2-5 mass parts is especially preferable.

  Furthermore, in the present invention, plasticizers, softeners, anti-aging agents, processing aids, lubricants, tackifiers and the like used in ordinary vulcanized rubber compounds are used in combination as long as the effect is not impaired. Is also good. Examples of softeners and plasticizers that are effective for adjusting moldability include process oils such as paraffin and naphthene, soft paraffin and other paraffins, waxes, synthetic polymer softeners such as silicone oil and liquid polybutene. Agents, ester plasticizers such as phthalic acid, adipic acid, sebacic acid and phosphoric acid, stearic acid and its esters, alkylsulfonic acid esters and tackifiers.

  The joint material of the present invention is obtained by kneading the above components using a known kneading apparatus such as a Banbury mixer, a kneader mixer, or a two-roll machine. It can be obtained by molding into a sheet by a known molding method. Further, from this sheet, a gasket is obtained by punching into a ring shape using a conventionally known device having a punching blade. This joint material is generally formed into a ring-shaped gasket and is inserted into a double-layer pipe or the like at the time of construction. However, when a double-layer pipe is manufactured, a tape-shaped product is wrapped around a vinyl chloride inner pipe in advance. In addition, it is possible to manufacture a fire-resistant double-layer pipe or the like integrally formed with a cement mortar outer pipe.

  Hereinafter, the present invention will be specifically described by way of examples. However, these examples do not limit the present invention. In addition, the part and% in the following description are based on a mass reference | standard.

  The components shown in Formulation A in Tables 1 and 2 were kneaded at 120 ° C. for 2 minutes using a 3 liter kneader mixer. Next, while kneading the obtained kneaded material with two rolls, the components shown in Table 1 and Table 2 are added and kneaded for 5 minutes, and further vulcanized at 170 ° C. for 4 minutes with a hot press. A joint material having a thickness of 5 mm was obtained.

The materials used in this example are as shown below.
(1) Rubber: Butyl rubber (manufactured by JSR Corporation, “butyl 268”), ethylene-propylene-diene rubber (manufactured by DSM Japan Ltd., “Keltan 778Z”)
(2) Thermally expandable graphite: (“SS-3” manufactured by Air Water Chemical Co., Ltd., expansion start temperature 260 ° C.)
(3) Aluminum phosphite: (Tahei Chemical Industry Co., Ltd., “APA-100”)
(4) Inorganic filler: Aluminum hydroxide ("ALH" manufactured by Kawai Lime Industry Co., Ltd.)
(5) Vulcanizing agent: Powdered sulfur (manufactured by Hosoi Chemical Co., Ltd.)
(6) Vulcanization accelerator: N-cyclohexyl-2-benzothiazylsulfenamide (manufactured by Ouchi Shinsei Co., Ltd., “Noxeller CZ”), tetramethylthiuram disulfide (manufactured by Shinsei Ouchi Co., Ltd., “Noxeller”) TT "), zinc oxide (manufactured by Sakai Chemical Co., Ltd.," Zinc Hana 3 ")
(7) Processing aid: Ester lubricant (manufactured by Kao Corporation, “Kaoh Wax 220”)
(8) Anti-aging agent: N- (1,3-dimethylbutyl) -N-phenyl-p-phenylenediamine (manufactured by Ouchi Shinsei Co., Ltd., “NOCRACK 6C”)
(9) Carbon black: “# 60” manufactured by Asahi Carbon Co., Ltd.
(10) Softener: Process oil (manufactured by Nippon Sun Oil Co., Ltd., “Thumper 150”)

"Examples 1-3""Comparative Examples 1-5"
In the examples and comparative examples, the following properties were evaluated and summarized in Tables 1 and 2.
The measuring method of each characteristic is shown below.
Tensile stress: A press-molded sheet having a thickness of 5 mm was punched into a No. 3 dumbbell and pulled at a speed of 500 mm / min to obtain the maximum stress.
Hardness: About the said sheet | seat, the durometer A hardness meter was used and the value immediately after pressing was read.
Flexibility: punched into a No. 1 dumbbell from a 5mm thick sheet molded with a roll, lifted both ends to a 45 degree angle, the degree of cracking when bent, "good" when no crack, crack The case where there was was evaluated as "impossible".
Thermal expansion: Refractory bricks with a thickness of 50 mm, a width of 100 mm, and a length of 210 mm are arranged with a gap of 10 mm, and a test piece with a thickness of 5 mm, a height of 70 mm, and a width of 50 mm is inserted between them. In this state, heat treatment was performed at 300 ° C. for 1 hour. When the 10 mm gap of the refractory brick was completely closed, it was evaluated as “good”, and when the gap remained, it was evaluated as “impossible”.
Shape retention: After evaluating the thermal expansion property, the shape stability and the degree of deformation of the test piece portion protruding from the upper end of the brick were evaluated by visual observation and finger touch. It was evaluated as “good” when it was difficult to lose its shape and deformation was small, “impossible” when it was deformed immediately by finger erosion, and “possible” in the middle.
Oxygen index: Measured using a combustion test apparatus (manufactured by Suga Test Instruments Co., Ltd., ON-1D type) according to JIS K7201.

As for the physical properties of the joint material, it is preferable that the tensile stress is 2.8 MPa or more, the hardness is 65 or more, and flexibility, thermal expansibility, and shape retention are good.

When the joint material of Comparative Example 2 using boric acid instead of aluminum phosphite is used, the hardness cannot be improved because boric acid has the property of inhibiting the vulcanization behavior. Also, since boric acid is water-soluble, if the joint material using this is used in a part that comes into contact with water for a long period of time, boric acid will elute from the joint material and have sufficient shape retention in the event of a fire. Although not obtained, aluminum phosphite is hardly soluble in water, so there is little concern.

Claims (4)

Vulcanizable rubber, thermally expandable graphite, aluminum phosphite, inorganic fillers, including a vulcanizing agent and a vulcanization accelerator state, and are an oxygen index more than 40 measured according to JIS K7201,
The vulcanizable rubber is butyl rubber and / or ethylene-propylene-diene rubber,
A joint material wherein the inorganic filler is aluminum hydroxide .   5-100 parts by mass of thermally expandable graphite, 10-150 parts by mass of aluminum phosphite, 10-200 parts by mass of inorganic filler, 0.1% of vulcanizing agent, relative to 100 parts by mass of vulcanizable rubber The joint material according to claim 1, which is 10 to 10 parts by mass and 0.1 to 10 parts by mass of the vulcanization accelerator. The joint material according to any one of claims 1 and 2, wherein the joint material is used between an opening edge of an outer pipe of a fireproof double-layer pipe and an opening edge of an outer pipe of a pipe joint facing the outer pipe. Joint material for fireproof double-layer pipes. The gasket which consists of a joint material of any one of Claims 1-3 .