Patent Application
20140203520
The present invention relates to a lip seal for water pump. More particularly, the present invention relates to a lip seal for water pump made of a rubber-like elastic material, fixed to a housing as a fixed side and in sliding contact with a shaft rotating relative to the housing.
In the case of lip seals used to seal aqueous fluids, such as LLC (long life coolant), the low lubricity of sliding surfaces causes significant abrasion due to sliding and leads to high heat generation. Organic acid-based LLC, particularly 2-ethylhexanoic acid-based LLC, causes significant softening and swelling of the lip seal, thus reducing sealing properties. Moreover, organic phosphoric acid-based LLC leads to accumulation of phosphoric acid compounds in the shaft and formation of a gap between the shaft and the lip seal, thus reducing sealing properties.
In order to improve lubricity in such a case, Patent Document 1 discloses a water pump sealing device using a lubricating grease for a lip lubricating.
More specifically, the water pump sealing device, which is fitted between a housing and a shaft so that a sealing fluid, such as LLC, does not leak from the inside of the device to the outside, can improve the lubricity of a seal lip sliding part to prevent the seal lip from being prematurely worn by slidable movement. In one structure, the sealing device comprises a plurality of seal lips and a grease-impregnating member impregnated with a lip-lubricating grease, wherein the grease-impregnating member is arranged in a space part between a plurality of the seal lips. In another structure, the sealing device comprises a sleeve secured to a shaft, first and second seal lips in sliding contact with the sleeve, a backup ring, and a grease-impregnating member, wherein the grease-impregnating member is arranged in a space that lies between the both seal lips and that is a radical direction gap part where the sleeve and the backup ring are radially opposed to each other.
Moreover, Patent Document 2 proposes a hydrogenated nitrile rubber composition comprising 100 parts by weight of hydrogenated nitrile rubber, and a total amount of about 120 parts by weight or more of carbon black and other filler, such as graphite, carbon fiber, silica, talc, clay, PTFE powder, activated carbon calcium, or calcium silicate. The hydrogenated nitrile rubber composition provides a crosslinked product having a thermal conductivity at 20° C. of 0.4 W/m·k or more and a 50% modulus of 14 MPa or more. Patent Document 2 indicates that the crosslinked product can significantly reduce the amount of heat generated during sliding, and thus can be suitably used as a sliding or high-pressure sealing material. However, when the crosslinked product is used as a lip seal to seal an aqueous-based fluid, such as LLC, the above-mentioned various properties inevitably decrease.
Furthermore, Patent Document 3 proposes an NBR composition comprising 100 parts by weight of NBR, 1 to 150 parts by weight of white carbon (silica), and 0.5 to 50 parts by weight of an inorganic compound having an average particle diameter of 2 μm or less and a Mohs hardness of 6 or more, such as aluminum oxide, silicon carbide, tungsten carbide, zirconium dioxide, iron oxide, titanium oxide, quartz powder, titanium nitride, titanium carbide, or zirconium carbide. Patent Document 3 indicates that a vulcanization-molded product of the NBR composition can achieve long life and energy saving when sealing materials are used in a sliding part, without impairing abrasion resistance. However, when the vulcanization-molded product is used as a lip seal to seal an aqueous-based fluid, such as LLC, the above-mentioned various properties inevitably decrease.
Patent Document 1: JP-A-2008-180342
Patent Document 2: JP-A-2002-080639
Patent Document 3: JP-A-2006-037044
An object of the present invention is to provide a lip seal for water pump made of a rubber-like elastic material, fixed to a housing as a fixed side and in sliding contact with a shaft rotating relative to the housing, the lip seal providing a materially solution, rather than a structural solution, to prevent softening and volume swelling of the rubber-like elastic material and the generation of deposits in the rotating shaft, which are problematic for rotation torque and LLC resistance.
The above object of the present invention can be achieved by the aforementioned lip seal for water pump made of a rubber-like elastic material; the lip seal being obtained by vulcanization-molding of a rubber composition comprising 100 parts by weight of the rubber-like elastic material, 1 to 150 parts by weight of a reinforcing filler, 5 to 90 parts by weight of a non-reinforcing filler having an average particle diameter of 1 μm or more, 0.1 to 5 parts by weight of a coupling agent, 1 to 15 parts by weight of a co-crosslinking agent, and 0.5 to 10 parts by weight of an organic peroxide.
According to the lip seal for water pump of the present invention, vulcanization molding of a rubber composition comprising a rubber-like elastic material, a reinforcing filler, a non-reinforcing filler having an average particle diameter of 1 μm or more, a coupling agent, a co-crosslinking agent, and an organic peroxide leads to effective prevention of softening and swelling of the rubber material caused by an aqueous-based fluid, such as LLC, and the generation of deposits in the rotating shaft.
Here, the use of the filler having an average particle diameter of 1 μm or more can prevent softening and volume swelling caused by osmosis of an aqueous fluid, such as LLC, while suppressing an increase in the hardness of the rubber-like elastic material. Moreover, due to the presence of the filler in the contact surface of shaft sliding surface, even when phosphoric acid-based LLC, which is likely to deposit in the shaft, is used, the deposits are cut because of the filler, so that no deposition is observed. Furthermore, a surface roughness Ra of about 1 to 30 μm is imparted to the sliding surface of the lip seal, and a liquid membrane is formed thereon to improve the lubrication state, thereby reducing torque. In addition, due to the reduced torque, heat generation by sliding can be reduced and abrasion can be prevented.
The presence of the coupling agent strengthens adhesion between the rubber and the filler, and prevents a phenomenon in which LLC is collected in the rubber/filler interface because of osmosis of LLC. As a result, softening and swelling are prevented. Moreover, since the volume effect of the filler relatively reduces the volume of the swollen rubber polymer, swelling is also prevented in this respect.
The use of the co-crosslinking agent leads to tight crosslinking, and softening and swelling caused by osmosis of LLC are prevented.
The rubber-like elastic material for forming the lip seal for water pump is at least one of any rubber-like elastic materials, such as nitrile rubber, hydrogenated nitrile rubber, EPDM, acrylic rubber, and fluororubber; among which hydrogenated nitrile rubber, EPDM, or fluororubber is preferably used.
Examples of the reinforcing filler include carbon black, silica, and the like. The proportion of reinforcing filler is 1 to 150 parts by weight, preferably 30 to 70 parts by weight, based on 100 parts by weight of the rubber-like elastic material. When the proportion of reinforcing filler is less than this range, the required rubber physical properties are not obtained; whereas when the proportion is greater than this range, the sealing properties of the rubber decrease.
The non-reinforcing filler may be any of various non-reinforcing fillers. Preferred examples thereof include silicates, such as aluminum silicate (Al2O3.SiO2), magnesium silicate (4SiO2.3MgO.H2O), and calcium silicate (CaSiO3); carbon fiber, iron oxide, titanium oxide, diatomaceous earth, and the like that have an average particle diameter (or the fiber diameter of the carbon fiber), as measured by laser analysis, of 1 μm or more, preferably 1 to 40 μm. The use of a non-reinforcing filler having such an average particle diameter can prevent softening and volume swelling caused by osmosis of LLC, while suppressing an increase in hardness. Moreover, due to the presence of such a filler in the sliding surface, deposits in the shaft generated when organic phosphorus acid-based LLC is used can be cut to prevent deposition. Furthermore, a roughness of about 1 to 30 μm is imparted to the sliding surface, and a liquid membrane is formed by the action of the roughness to improve the lubrication state. Consequently, torque and sliding heat generation can be reduced, and abrasion can be prevented.
In contrast, when a non-reinforcing filler having an average particle diameter of less than 1 μm is used, the cutting effect of deposits becomes low, and sealing properties cannot be ensured when organic phosphorus acid-based LLC is used. Further, the liquid membrane forming ability is lowered, thereby leading to worsening of the lubrication state.
The proportion of non-reinforcing filler is 5 to 90 parts by weight, preferably 5 to 70 parts by weight, based on 100 parts by weight of the rubber-like elastic material. When the proportion of filler is less than this range, the desired effect of the present invention cannot be obtained; whereas when the proportion is greater than this range, the physical property evaluation (elongation at break) is low.
The coupling agent may be a silane-, titanium-, zirconium- or aluminum coupling agent; among which a silane-based coupling agent is preferably used.
Examples of silane-based coupling agents include vinyl-, glycidoxy-, methacryloxy-, and amino-based silane coupling agents, such as vinyltrichlorosilane, vinyltrimetoxysilane, vinylethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 3-glycidoxypropyltrimetoxysilane, 3-glycidoxypropylmethyldiethoxysilane, p-styryltrimethoxysilane, 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, N-2-(aminoethyl)-3-aminopropylmethyldimethoxysilane, 3-aminopropyltrimethoxysilane, and N-phenyl-3-aminopropyltrimethoxysilane. Examples of titanium-based coupling agents include titanium diisopropoxybis(triethanolaminate), titanium lactate ammonium salt, titanium lactate, titanium dioctyloxybis(octyleneglycolate), and the like. Examples of zirconium-based coupling agents include zirconium tetra-n-butoxide, zirconium tetra-acetylacetonate, zirconium tributoxymonoacetylacetonate, zirconium monobutoxy acetylacetonatebis(ethylacetoacetate), zirconium butoxybis(ethylacetoacetate), zirconium tetraacetylacetonate, zirconium tributoxymonostearate, and the like. Moreover, examples of aluminum-based coupling agents include acetoalkoxy aluminum diisopropylate, and the like.
The proportion of coupling agent is 0.1 to 5 parts by weight, preferably 0.5 to 3 parts by weight, based on 100 parts by weight of the rubber-like elastic material. When the proportion of coupling agent is less than this range, the dipping test will show inferior results; whereas when the proportion is greater than this range, physical properties, such as elongation at break, decrease.
Examples of the organic peroxide include 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, t-butylperoxy benzoate, t-butylperoxy isopropyl carbonate, n-butyl-4,4′-di(t-butylperoxy)valerate, and the like. The proportion of organic peroxide is 0.5 to 10 parts by weight, preferably 1 to 8 parts by weight, based on 100 parts by weight of the rubber-like elastic material.
When performing organic peroxide crosslinking, a polyfunctional unsaturated compound, such as triallyl isocyanurate, triallyl cyanurate, triallyl trimellitate, trimethylolpropane trimethacrylate, or N,N′-m-phenylenebismaleimide, is used as a co-crosslinking agent. The proportion of co-crosslinking agent is 1 to 15 parts by weight, preferably 2 to 10 parts by weight, based on 100 parts by weight of the rubber-like elastic material. When the proportion of co-crosslinking agent is less than this range, the dipping test will show inferior results, that is, softening and swelling cannot be sufficiently prevented. In contrast, when the proportion is greater than this range, the evaluation of physical properties, such as elongation at break, will be inferior.
The composition comprising the above components may suitably contain processing aids, such as stearic acid, palmitic acid, and paraffin wax; acid acceptors, such as zinc oxide, magnesium oxide, and hydrotalcite; antioxidants; plasticizers; and other compounding agents that are generally used in the rubber industry, if necessary.
The preparation of the rubber composition is carried out by kneading the components by using an open roll or a kneading machine such as intermix, kneader, or Banbury mixer. Crosslinking of the kneaded product is generally carried out by heating at about 150 to 200° C. for about 3 to 60 minutes using an injection molding machine, compression molding machine, vulcanizing press, or the like, optionally followed by secondary crosslinking by heating at about 100 to 200° C. for about 1 to 24 hours.
Due to the presence of the filler having an average particle diameter of 1 μm or more, the sliding surface of the vulcanization-molded lip seal has concave-convex portions irregularities with a surface roughness Ra (arithmetic average height defined by JIS B 0601) of 1 to 30 μm. Therefore, when the lip seal is used as a lip seal made of a rubber-like elastic material, fixed to a housing as a fixed side and in sliding contact with a shaft rotating relative to the housing, the aforementioned various effects can be obtained.
The following describes the present invention with reference to Examples.
The above components were kneaded by a 10-inch roll, and the knead product was subjected to primary vulcanization at 180° C. for 5 minutes and oven vulcanization (secondary vulcanization) at 150° C. for 1 hour, thereby vulcanization-molding a rubber sheet (thickness: 2 mm) and a lip seal (sliding surface roughness Ra: 4 μm).
The obtained crosslinked products were measured by the following items. Regarding test pieces, the rubber sheet was used in the physical property evaluation and the dipping test, and the lip seal was used in the torque test and the deposition test.
In Example 1, the amount of aluminum silicate was changed to 5 parts by weight.
In Example 1, the amount of aluminum silicate was changed to 70 parts by weight.
In Example 1, the amount of aluminum silicate was changed to 30 parts by weight, and 15 parts by weight of carbon fiber (Donacarbo S-241, produced by Osaka Gas Chemicals Co., Ltd.; fiber diameter: 13 μm, fiber length: 130 μm) was further used.
In Example 1, the same amount (100 parts by weight) of EPDM (EPT3045, produced by Mitsui Chemicals, Inc.) was used in place of hydrogenated nitrile rubber.
Using the above components, kneading, vulcanization-molding, and measurement were performed in the same manner as in Example 1.
In Example 1, the same amount (15 parts by weight) of calcium silicate (NYAD 1250, produced by NYCO Minerals, Inc.; average particle diameter: 4.5 μm) was used in place of aluminum silicate.
In Example 4, the same amount (30 parts by weight) of calcium silicate (NYAD 1250) was used in place of aluminum silicate.
Table 1 below shows the evaluation results obtained in the Examples, together with the amount of each component (unit: part by weight).
In Example 1, the same amount (15 parts by weight) of clay (Hydrite, produced by Takehara Kagaku Kogyo Co., Ltd.; average particle diameter: 0.68 μm) was used in place of aluminum silicate.
In Example 1, the amount of aluminum silicate was changed to 100 parts by weight.
In Example 1, the amount of co-crosslinking agent A was changed to 20 parts by weight.
In Example 1, no silane-based coupling agent was used.
In Example 1, no co-crosslinking agent A was used.
In Example 1, none of aluminum silicate, silane-based coupling agent, and co-crosslinking agent A was used.
Table 2 below shows the evaluation results obtained in the Comparative Examples, together with the amount of each component (unit: part by weight).
| Number | Date | Country | Kind |
|---|---|---|---|
| 2011-197310 | Sep 2011 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2012/072467 | 9/4/2012 | WO | 00 | 2/14/2014 |
