Sealing member for mechanical seals

Abstract

A sealing member for mechanical seals, which is a peroxide vulcanized molded article of a hydrogenated nitrile rubber having a bound acrylonitrile content of less than 20% and an iodine number of 20 mg/100 g or less. The sealing member for mechanical seals is obtained as a peroxide vulcanized molded article of a hydrogenated nitrile rubber composition comprising 0 to 5 parts by weight of carbon black, 20 to 100 parts by weight of silica, and 0.5 to 3 parts by weight of silane coupling agent, based on 100 parts by weight of hydrogenated nitrile rubber, and preferably further compounding 50 parts by weight or less of titanium oxide non-reinforcing filler. The obtained vulcanized molded article is to provide a sealing member for mechanical seals that can achieve desired LLC resistance, and that has excellent compression set characteristics, cold resistance, processability, hardness, etc.

Claims

1. A static sealing member, which is a peroxide vulcanized molded article of a hydrogenated nitrile rubber composition comprising 20 to 100 parts by weight of silica and 0.5 to 3 parts by weight of silane coupling agent, based on 100 parts by weight of hydrogenated nitrile rubber having a bound acrylonitrile content of less than 20% and an iodine number of 20 mg/100 g or less, wherein the static sealing member is a cup gasket or a bellows of a mechanical seal of a water pump.

2. The static sealing member for mechanical seals according to claim 1, wherein the hydrogenated nitrile rubber composition, in which 5 parts by weight or less of carbon black is further compounded, is used.

3. The sealing member for mechanical seals according to claim 2, which has a volume change rate of 4% or less after dipping in a 30 volume % LLC aqueous solution at 150° C. for 300 hours.

4. The static sealing member for mechanical seals according to claim 1, wherein the hydrogenated nitrile rubber composition, in which 50 parts by weight or less of titanium oxide non-reinforcing filler is further compounded, is used.

5. The sealing member for mechanical seals according to claim 4, which has a volume change rate of 4% or less after dipping in a 30 volume % LLC aqueous solution at 150° C. for 300 hours.

6. The sealing member for mechanical seals according to claim 1, which has a volume change rate of 4% or less after dipping in a 30 volume % LLC aqueous solution at 150° C. for 300 hours.

Description

EMBODIMENTS FOR CARRYING OUT THE INVENTION

(1) As hydrogenated NBR, one having a bound AN content of less than 20%, preferably 19 to 17%, and an iodine number of 20 mg/100 g or less, preferably 15 to 10 mg/100 g, is used. In practice, commercial products, such as the Zetpol series 4300, 4310, and 4320 (produced by Zeon Corporation), are used.

(2) Patent Document 5 describes the use of hydrogenated NBR having a bound AN content of 15 to 30%, preferably 20 to 25%, and Patent Document 6 describes the use of hydrogenated NBR having an AN content of 15 to 50%, preferably 20 to 45%; however, these documents do not provide Examples using hydrogenated NBR having an AN content of less than 20%.

(3) As silica, either of dry process silica and wet process silica can be used. Silica having a specific surface area of about 20 to 200 m.sup.2/g is generally used. In practice, commercial products, such as Nipseal LP (produced by Tosoh Silica Corporation) and Ultrasil 360 (produced by Evonik Degussa), are used.

(4) Silica is used at a ratio of about 20 to 100 parts by weight, preferably about 25 to 80 parts by weight, based on 100 parts by weight of hydrogenated NBR, and is used at various ratios depending on the required product hardness. If the compounding ratio of silica is less than this range, the hardness of the vulcanizate becomes too low. In contrast, if silica is used at a ratio greater than this range, the hardness of the vulcanizate becomes too high.

(5) As long as the object of the present invention is not inhibited, and in an amount to the extent of giving coloring, it is allowed to compound about 5 parts by weight or less of carbon black based on 100 parts by weight of hydrogenated NBR.

(6) Examples of the silane-based coupling agent include vinyl group-, epoxy group-, or amino group-containing silane coupling agents, such as vinyltrichlorosilane, vinyltrimethoxysilane, vinyltriethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, N-2-(aminoethyl)-3-aminopropylmethyldimethoxysilane, 3-aminopropyltrimethoxysilane, and N-phenyl-3-aminopropyltrimethoxysilane.

(7) The silane-based coupling agent is used at a ratio of about 0.5 to 3 parts by weight, preferably about 0.5 to 1 part by weight, based on 100 parts by weight of hydrogenated NBR. If the compounding ratio of the silane-based coupling agent is less than this range, sufficient LLC resistance of the vulcanizate cannot the achieved. In contrast, if the silane-based coupling agent is used at a ratio greater than this range, the elongation of the vulcanizate is significantly reduced.

(8) By compounding in the composition titanium oxide TiO.sub.2 having an average particle diameter of about 0.05 to 10 μm at a ratio of about 50 parts by weight or less, preferably about 25 to 50 parts by weight, LLC resistance is further improved. Although titanium oxide is also used in Patent Documents 4 and 9, it is not to improve LLC resistance.

(9) Examples of the organic peroxide include di-t-butyl peroxide, dicumyl peroxide, t-butylcumyl peroxide, 1,1-di(t-butylperoxy)-3,3,5-trimethylcyclohexane, 2,5-dimethyl-2,5-di(t-butylperoxy)hexane, 2,5-dimethyl-2,5-di(t-butylperoxy)hexyne-3,1,3-di(t-butylperoxyisopropyl)benzene, 2,5-dimethyl-2,5-di(benzoylperoxy)hexane, butylperoxy benzoate, t-butylperoxy isopropyl carbonate, n-butyl-4,4′-di(t-butylperoxy) valerate, and the like. The organic peroxide is used at a ratio of about 1 to 10 parts by weight, preferably about 2 to 8 parts by weight, based on 100 parts by weight of the hydrogenated NBR. When the compounding amount of organic peroxide is less than this range, any vulcanizate having sufficient crosslinking density cannot be obtained. In contrast, when the compounding amount is greater than this range, foaming occurs, and vulcanization-molding cannot be performed; or, if vulcanization-molding can be performed, rubber elasticity and elongation decrease.

(10) Furthermore, preferred examples of the polyfunctional unsaturated compound co-crosslinking agent include difunctional or trifunctional (meth)acrylates, such as ethyleneglycol dimethacrylate, triethyleneglycol dimethacrylate, 1,4-butyleneglycol dimethacrylate, 1,6-hexanediol dimethacrylate, and trimethylolpropane trimethacrylate. Allyl-based co-crosslinking agents that are generally used in combination with organic peroxides, such as triallyl isocyanurate, triallyl cyanurate, triallyl trimellitate, and diallyl isocyanurate, can also be used. The term “(meth)acrylate” as used herein refers to acrylate or methacrylate.

(11) The polyfunctional unsaturated compound co-crosslinking agent is used at a ratio of about 30 parts by weight or less, preferably 1 to 10 parts by weight, based on 100 parts by weight of the hydrogenated nitrile rubber.

(12) The composition is prepared in the following manner. In addition to each of the above components, various compounding agents generally used in the rubber industry, such as processing aids (e.g., stearic acid, palmitic acid, or paraffin wax), acid acceptors (e.g., zinc oxide, magnesium oxide, or hydrotalcite), and antiaging agents, are suitably compounded (provided that the amount of plasticizer is 30 parts by weight or less), and the resulting mixture is kneaded using a kneading machine, such as an intermix, a kneader, or a Banbury mixer, and an open roll. The kneaded product is vulcanized generally by heating at about 150 to 200° C. for about 3 to 60 minutes using an injection molding machine, a compression molding machine, a vulcanization press, or the like, further optionally followed by oven vulcanization (secondary vulcanization) by heating at about 120 to 200° C. for about 1 to 24 hours, thereby vulcanization molding the resultant into a target product, i.e., a cup gasket or bellows of a mechanical seal for water pumps.

EXAMPLES

(13) The following describes the present invention with reference to Examples.

Example 1

(14) TABLE-US-00001 Hydrogenated NBR-A (Zetpol 4310, produced by 100 parts by weight Zeon Corporation; AN content: 19%, iodine value: 15 mg/100 mg) Silica (Nipsil LP, produced by 80 parts by weight Tosoh Silica Corporation; specific surface area: 207 m.sup.2/g) Silane-based coupling agent (A-151NTJ SILANE, 1 part by weight produced by Momentive Performance Materials Inc.) Organic peroxide (Percumyl D, produced by 5 parts by weight NOF Corporation)
The above components were kneaded with a kneader and an open roll. The kneaded product (composition) was then subjected to press vulcanization at 180° C. for 6 minutes, and a vulcanized sheet (150×150×2 mm) was obtained.

(15) The obtained vulcanized sheet and P-24 O ring were measured for each of the following items.

(16) LLC resistance: The volume change rate after dipping in a 30 volume % LLC (JCC273K, produced by Japan Chemical Industries Co., Ltd.) aqueous solution at 150° C. for 300 hours was measured. A volume change rate of less than 2% was evaluated as ⊚, that of 2 to 4% was evaluated as ◯, and that of 5% or more was evaluated as ×.

(17) Compression set (CS): The compression set was measured at 120° C. for 70 hours according to JIS K6262 corresponding to ASTM D395. A compression set of less than 10% was evaluated as ⊚, that of 10 to 12% was evaluated as Δ, and that exceeding 12% was evaluated as ×.

(18) Cold resistance: The glass transition point Tg was measured. A glass transition point of lower than −35° C. was evaluated as ◯, and that of −34° C. or higher was evaluated as ×.

(19) Processability: Kneading properties (kneader discharge properties) and moldability were compared and evaluated. When the kneader discharge properties and molding evaluation were both excellent, this case was evaluated as ◯; when the kneader discharge properties were excellent, while the molding evaluation was defective, this case was evaluated as Δ; and when both were defective, this case was evaluated as ×. Hardness: according to JIS K6253 corresponding to ASTM D2240. Examples 1 to 6 are examples of high hardness (75 to 80), and Examples 7 to 9 are examples of low hardness (60).

Example 2

(20) In Example 1, the same amount (100 parts by weight) of hydrogenated NBR-B (THERBAN 1707, produced by ARLANXEO; AN content: 17%) was used in place of the hydrogenated NBR-A.

Example 3

(21) In Example 1, the amount of the silica was changed to 75 parts by weight, and 3 parts by weight of MT carbon black (THERMAX N990, produced by Cancarb Limited) and 30 parts by weight of titanium oxide (TIPAQUE A-100, produced by ISHIHARA SANGYO KAISHA, LTD.; an average particle diameter of 0.15 μm) were further compounded.

Example 4

(22) In Example 1, the amount of the silica was changed to 70 parts by weight, and 5 parts by weight of MT carbon black (THERMAX N990) and 50 parts by weight of titanium oxide (TIPAQUE A-100) were further compounded.

Example 5

(23) In Example 1, the amount of the silica was changed to 70 parts by weight.

Example 6

(24) In Example 5, the amount of the silica was changed to 60 parts by weight, and 3 parts by weight of MT carbon black and 30 parts by weight of titanium oxide were further compounded.

Example 7

(25) In Example 5, the amount of the silica was changed to 55 parts by weight, and 5 parts by weight of MT carbon black and 50 parts by weight of titanium oxide were further compounded.

Example 8

(26) In Example 1, the amount of the silica was changed to 45 parts by weight.

Example 9

(27) In Example 8, the amount of the silica was changed to 35 parts by weight, and 2 parts by weight of MT carbon black and 25 parts by weight of titanium oxide were further compounded.

Example 10

(28) In Example 8, the amount of the silica was changed to 25 parts by weight, and 2 parts by weight of MT carbon black and 50 parts by weight of titanium oxide were further compounded.

Comparative Example 1

(29) In Example 1, the same amount (100 parts by weight) of hydrogenated NBR-C (Zetpol 3110, produced by Zeon Corporation; AN content: 25%, iodine value: 15 mg/100 mg) was used in place of the hydrogenated NBR-A.

Comparative Example 2

(30) In Example 1, the same amount (100 parts by weight) of hydrogenated NBR-C (Zetpol 3110) was used in place of the hydrogenated NBR-A, 90 parts by weight of MT carbon black was used in place of the silica and the silane coupling agent.

Comparative Example 3

(31) In Example 1, 40 parts by weight of SRF carbon black (SEAST G-S, produced by Tokai Carbon Co., Ltd.) was used in place of the silica and the silane coupling agent.

Comparative Example 4

(32) In Example 1, 125 parts by weight of SRF carbon black (SEAST G-S) was used in place of the silica and the silane coupling agent.

Comparative Example 5

(33) In Example 1, 60 parts by weight of MT carbon black was used in place of the silica and the silane coupling agent.

Comparative Example 6

(34) In Example 1, 140 parts by weight of MT carbon black was used in place of the silica and the silane coupling agent.

Comparative Example 7

(35) In Example 1, 50 parts by weight of MT carbon black was used in place of the silica and the silane coupling agent, and 30 parts by weight of titanium oxide was further compounded.

Comparative Example 8

(36) In Example 1, 50 parts by weight of MT carbon black was used in place of the silica and the silane coupling agent, and 30 parts by weight of calcium carbonate (Hakuenka CC, produced by Shiraishi Calcium Kaisha, Ltd.) was further compounded.

Comparative Example 9

(37) In Example 1, 50 parts by weight of MT carbon black was used in place of the silica and the silane coupling agent, and 30 parts by weight of cellulose powder (KC FLOCK W-250 produced by Nippon Paper Industries Co., Ltd.) was further compounded.

Comparative Example 10

(38) In Example 1, 50 parts by weight of MT carbon black was used in place of the silica and the silane coupling agent, and 30 parts by weight of barium sulfate (produced by Sakai Chemical Industry Co., Ltd.) was further compounded.

(39) Table below shows the evaluation and measurement results obtained in Examples and Comparative Examples.

(40) TABLE-US-00002 TABLE LLC Cold Example resistance CS resistance Processability Hardness Example 1 ◯ ◯ ◯ ◯ 80 Example 2 ◯ ◯ ◯ ◯ 80 Example 3 ⊚ ◯ ◯ ◯ 80 Example 4 ⊚ ◯ ◯ ◯ 80 Example 5 ◯ ◯ ◯ ◯ 75 Example 6 ◯ ◯ ◯ ◯ 75 Example 7 ◯ ◯ ◯ ◯ 75 Example 8 ◯ ◯ ◯ ◯ 60 Example 9 ◯ ◯ ◯ ◯ 60 Example 10 ◯ ◯ ◯ ◯ 60 Comparative ◯ ◯ X Δ 80 Example 1 Comparative ◯ ◯ X ◯ 60 Example 2 Comparative X ◯ ◯ X 60 Example 3 Comparative X ◯ ◯ ◯ 85 Example 4 Comparative ◯ ◯ ◯ X 55 Example 5 Comparative X ◯ ◯ ◯ 75 Example 6 Comparative ◯ Δ ◯ Δ 70 Example 7 Comparative ◯ X ◯ Δ 70 Example 8 Comparative X X ◯ Δ 75 Example 9 Comparative X ◯ ◯ Δ 70 Example 10