[go: up one dir, main page]

US20030220421A1 - Low noise synthetic resin composition and method - Google Patents

Low noise synthetic resin composition and method Download PDF

Info

Publication number
US20030220421A1
US20030220421A1 US10/377,964 US37796403A US2003220421A1 US 20030220421 A1 US20030220421 A1 US 20030220421A1 US 37796403 A US37796403 A US 37796403A US 2003220421 A1 US2003220421 A1 US 2003220421A1
Authority
US
United States
Prior art keywords
article
manufacture
resin
rbc
crbc
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US10/377,964
Inventor
Kazuo Hokkirigawa
Motoharu Akiyama
Morinobu Kawamura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Minebea Co Ltd
Original Assignee
Minebea Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2002055308A external-priority patent/JP2003253132A/en
Priority claimed from JP2002062406A external-priority patent/JP4031266B2/en
Priority claimed from JP2002062412A external-priority patent/JP2003263923A/en
Priority claimed from JP2002176436A external-priority patent/JP2004018700A/en
Priority claimed from JP2002272147A external-priority patent/JP2004108499A/en
Application filed by Minebea Co Ltd filed Critical Minebea Co Ltd
Assigned to MINEBEA CO., LTD. reassignment MINEBEA CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HOKKIRIGAWA, KAZUO, KAWAMURA, MORINOBU, AKIYAMA, MOTOHARU
Assigned to MINEBEA CO., LTD. reassignment MINEBEA CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HOKKIRIGAWA, KAZUO, AKIYAMA, MOTOHARU, KAWAMURA, MORINOBU
Publication of US20030220421A1 publication Critical patent/US20030220421A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/02Parts of sliding-contact bearings
    • F16C33/04Brasses; Bushes; Linings
    • F16C33/20Sliding surface consisting mainly of plastics
    • F16C33/201Composition of the plastic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/04Carbon
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C17/00Sliding-contact bearings for exclusively rotary movement
    • F16C17/12Sliding-contact bearings for exclusively rotary movement characterised by features not related to the direction of the load
    • F16C17/14Sliding-contact bearings for exclusively rotary movement characterised by features not related to the direction of the load specially adapted for operating in water
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/02Parts of sliding-contact bearings
    • F16C33/04Brasses; Bushes; Linings
    • F16C33/043Sliding surface consisting mainly of ceramics, cermets or hard carbon, e.g. diamond like carbon [DLC]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S384/00Bearings
    • Y10S384/90Cooling or heating
    • Y10S384/907Bearing material or solid lubricant

Definitions

  • the present invention relates to synthetic resin compositions. More particularly, the present invention relates to synthetic resin compositions that can be molded into articles that generate less noise in use.
  • ⁇ D ⁇ D ⁇ n, where f k is the dynamic friction force and n is the normal force pressing the surfaces together.
  • ⁇ D may be measured by determining the ratio f k /n.
  • the dynamic friction force and the coefficient of dynamic friction approach a constant value as the sliding speed, v s , approaches a high velocity, for example greater than 1 meter per second (m/s).
  • the coefficient of dynamic friction is independent of the sliding speed, v s .
  • the coefficient of dynamic friction, ⁇ D is speed dependent.
  • the dynamic friction force, f k approaches a maximum as the sliding speed, v s , approaches 0.
  • the sliding speed, v s is 0, then the two surfaces are at rest with each other, and the measured friction force is defined as a static friction force.
  • the maximum static friction force, f max occurs immediately prior to the onset of sliding.
  • a large difference between f max and f k (v 2 ⁇ ) results in stick-slip behavior that causes excessive noise in mechanical devices that use the material. Thus, it is desirable to have a material with little or no stick-slip behavior.
  • the stick-slip phenomenon may be understood by a perusal of FIGS. 1 and 2 which show a device used for placing a certain load W at a tip 2 ′ of a stick 2 .
  • Stick 2 is held by a bearing 4 in a freely rotatable fashion on a disc 1 made of the testing material.
  • a spring 3 is fixed at the intermediate part of stick 2 .
  • Disk 1 is rotated in the direction indicated by the arrow mark by means of a driving device 5 .
  • the stick-slip phenomenon is created by the difference between the static friction coefficient ⁇ S and the dynamic friction coefficient ⁇ D .
  • the stick slip phenomenon is manifested as noise in a machine device using the machine element.
  • the present invention relates to a synthetic resin composition for preventing noise in finished parts molded from the composition.
  • the materials have a small difference between their static friction coefficient, ⁇ S , and their dynamic friction coefficient, ⁇ D . This substantially reduces the “stick-slip phenomenon”, which is the source of noise in engineering plastics, such as polyacetal and the like.
  • the present invention is directed to a low noise composition comprising fine particles of RBC or CRBC uniformly dispersed in a synthetic resin.
  • the present invention is directed to an article of manufacture comprising a molded low noise synthetic resin composition comprising fine particles of RBC or CRBC uniformly dispersed in a synthetic resin.
  • FIG. 1 is an oblique view of the equipment for measuring the stick-slip phenomenon.
  • FIG. 2 is a cross section of the equipment for measuring the stick-slip phenomenon.
  • FIG. 3 is a graph depicting the friction characteristics of a polyacetal molded product (“RBC/POM”).
  • FIG. 4 is a graph depicting the friction characteristics of a polyamide (nylon 66) molded product (“RBC/PA66”).
  • FIG. 5 is a graph depicting the friction characteristics of a polyamide (nylon 66) molded product containing glass fibers (“RBC/GF23PA66”).
  • FIG. 6 is a graph depicting the friction characteristics of a polyamide (nylon 11) molded product (“CRBC/PA11”).
  • FIG. 7 is a graph depicting the friction characteristics of a polybutylene terephthalate molded product (“CRBC/PBT”).
  • FIG. 8 is a graph depicting the friction characteristics of a polypropylene molded product (“CRBC/PP”).
  • RBC rice bran ceramic
  • CRBC carbonized rice bran ceramic
  • rice bran is preferably used as a starting material because of its low cost. Large quantities are produced as a by-product of other processes, e.g., about 900,000 tons per year in Japan alone and 33,000,000 tons per year throughout the world.
  • RBC is a carbon material made, for example, by mixing and kneading a de-fatted rice bran (de-fatted bran obtained from rice) with a thermally hardening or thermosetting resin, molding a product from the mixture, drying it, and then firing the dried molded product in an inert gas atmosphere, e.g., sintering.
  • a de-fatted rice bran de-fatted bran obtained from rice
  • thermosetting resin e.g., sintering.
  • thermosetting resin that is mixed with the de-fatted rice bran should be any resin that is heat hardened or cured by heating.
  • Preferred resins include, but not limited to, phenolics, diaryl phthalate resins, unsaturated polyester resins, epoxies, polyimides, triazine resins and the like. Phenolic resins, e.g., resols, are especially preferred.
  • the mixing ratio of de-fatted rice bran to the thermosetting resin should be in the range from about 50 to 90:50 to 10 (about 50:50 to about 90:10) by weight. A ratio of about 75:25 is especially preferred.
  • CRBC is a carbon material also obtained from defatted rice bran and a thermosetting resin
  • bus is an improvement over RBC.
  • the de-fatted rice bran and the thermosetting resin are mixed, kneaded, and then first fired in an inert gas atmosphere at a temperature in the range of about 700° C. to 1000° C., e.g., sintered. Ordinarily, the mixture is fired in a rotary kiln for a period of about 40 to about 120 minutes. The resulting material is then pulverized (crushed) into to less than about 100 mesh to form carbonized powder.
  • thermosetting resin which may be, but is not necessarily, the same as that employed with the de-fatted rice bran, and kneaded.
  • This product is then molded under pressure in the range of about 20 Mpa to 30 Mpa.
  • the molded product is once again heat treated in an inert gas atmosphere at a temperature in the range from about 100° to 1100° C., e.g., sintered, thereby obtaining a black resin or porous CRBC ceramic.
  • fine particles of RBC or CRBC are mixed with a synthetic resin to form a synthetic resin composite having unique and useful friction characteristics.
  • the RBC or CRBC constitutes about 30-70% by weight of the entire synthetic resin composite.
  • the weight ratio of the RBC or CRBC particles to the synthetic resin is about 30 to 90:70 to 10 (about 30:70 to about 90:10).
  • the RBC or CRBC particles are uniformly dispersed in a synthetic resin.
  • the fine particles are uniformly dispersed by mixing them with the synthetic resin at or near the resin's fusion point, followed by kneading.
  • the weight ratio of the particles to the synthetic resin is about 30 to 90:70 to 10 (about 30:70 to about 90:10), the difference between the static friction coefficient ⁇ S and the dynamic friction coefficient ⁇ D on the surface of an article molded from the composition is reduced.
  • the RBC or CRBC should have a mean particle size of about 300 ⁇ m or less, preferably a mean particle size of about 20-150 ⁇ m. It has been found that a synthetic resin composite of the present invention including fine particles of RBC or CRBC, results in a composition that has surface characteristics that make the composition particularly suitable for use in low noise applications.
  • the synthetic resins that are mixed with the RBC or CRBC are thermoplastic resins.
  • these resins include, but are not limited to, polyacetal, polyamide, polyester, polyolefins, and the like.
  • POM polyacetal, i.e., polyoxymethylene
  • nylon 66 polyhexamethylene adipamide
  • nylon 6 polycapramide
  • nylon 11 polyundecanamide
  • nylon 12 polybutylene terephthalate, polyethylene teraphthalate, polypropylene, polyethylene, and other thermoplastic resins are preferred.
  • POM, nylon 66, nylon 11, polybutylene terephthalate, polypropylene, polyethylene, and other thermoplastic resins are preferred.
  • These thermoplastic resins can be used either alone or in combination.
  • thermoplastic resin or resins can be used in combination with one or more thermosetting resins.
  • thermosetting resins that can be used in the present invention include, but are not limited to, phenolics, diaryl phthalate resins, unsaturated polyester resins, epoxies, polyimides, triazine resins system, and the like.
  • the RBC or CRBC should constitute about 30-70% by weight of the synthetic composition.
  • the weight ratio of the fine particles of RBC or CRBC to the synthetic resin should be about 30 to 90:70 to 10. It has been found that if the synthetic resin exceeds about 70 weight percent, the difference between the static friction coefficient ⁇ S and the dynamic friction coefficient ⁇ D becomes too large. On the other hand, if it is less than about 10 weight percent, molding becomes difficult.
  • the low noise synthetic resin composition of the present invention can be molded into any given shape by any of the known methods.
  • the molded compositions are used in the manufacture of machine elements, such as, for example, screws, bearings, axial relays, cam mechanisms, cylinders and pistons, wheels, belts and pulleys, chains and sprockets, valves and tubes, and the like.
  • molding is carried out by extrusion molding, injection molding or by any of the known methods.
  • the temperature of the mold should be relatively low, preferably in the range between the glass transition point of the synthetic resin and its fusion point. It is also preferred that the mold be cooled gradually rather than suddenly, which will normally provide a molded product having superior surface conditions.
  • the strength of the molded product can be increased by adding inorganic fibers, such as glass fiber, rock wool, carbon fibers, and the like; synthetic fibers, such as polyester, rayon, polyvinyl alcohol, polyamide, polyolefin, acrylic, and the like; or natural pulp fibers, such as wood pulp, Manila hemp, and the like.
  • inorganic fibers such as glass fiber, rock wool, carbon fibers, and the like
  • synthetic fibers such as polyester, rayon, polyvinyl alcohol, polyamide, polyolefin, acrylic, and the like
  • natural pulp fibers such as wood pulp, Manila hemp, and the like.
  • Examples 1-9 include materials made with and without RBC or CRBC as an additive. The friction characteristics of each of the examples was then measured, and the examples without RBC or CRBC as additives were compared to examples with RBC or CRBC as an additive.
  • FIGS. 3 - 8 each show the dynamic friction coefficient, ⁇ D versus the slide speed, v s , for Examples 1-9 (materials with and without RBC or CRBC particulate additives). Measurements were made of the dynamic coefficient of friction, ⁇ D , over a range of sliding speeds, v s , from 0.001 m/s to 1.0 m/s for various materials, e.g., in the range of 0.001-0.01 m/s and 0.1-1 m/s. A normal force, n, of 0.49 Newtons (N) was applied, pressing a SUJ ball with a diameter of 2 millimeters (mm) into contact with the surface of a specimen.
  • N normal force
  • a reciprocating friction test apparatus was used to measure the dynamic friction force for sliding speeds in the range from 0.001 m/s to 0.01 m/s, and a rotary friction test apparatus was used to measure the dynamic friction force, f k , at higher velocities from 0.1 m/s to 1 m/s.
  • the reciprocating arm repeated 1000 strokes and the stroke distance was 5 mm, which was a distance sufficient to reach a steady measurement of the dynamic friction force, f k , which was used to calculate ⁇ D .
  • the specimens were prepared by injecting heated materials into a metal mould to produce a circular specimen with a diameter of 50 mm and a thickness of 3 mm.
  • the injection temperature varied, depending on the compositions of the materials used in each of the examples, as noted below.
  • An ester lubricating oil was applied to surface of the material prior to each test.
  • FIGS. 3 - 8 demonstrate that the materials without RBC or CRBC particulate additives show stick-slip behavior, and the materials with RBC or CRBC particulate additives show little or no stick-slip behavior. Instead, materials with RBC or CRBC particulate additives show a nearly constant dynamic friction coefficient, ⁇ D , over the full range of slide speeds tested, even at sliding speeds as low as 0.001 m/s. Thus, the specific examples described below indicate that materials with RBC or CRBC particulate additives reduce stick-slip behavior, avoiding the generation of noise.
  • the mixture was fired in a rotary kiln for 120 minutes at 900° C. in a nitrogen atmosphere.
  • the resulting carbonized product was sifted through a 170-mesh sieve. Fine RBC particles having a mean particle size in the range of 145 to 155 ⁇ m were obtained.
  • the mixture was fired at 1,000° C. for 120 minutes in a rotary kiln in a nitrogen atmosphere.
  • the resulting carbonized product was sifted through a 170-mesh sieve yielding RBC particles having a mean particle size in the range of from 145 to 155 ⁇ m.
  • the mixture was fired at 900° C. for 120 minutes in a rotary kiln in a nitrogen atmosphere.
  • the resulting carbonized product was pulverized and sifted through an 800-mesh sieve yielding RBC particles having a mean particle size of 30 ⁇ m.
  • the mixture was fired at 900° C. for 100 minutes in a rotary kiln in a nitrogen atmosphere.
  • the resulting carbonized product was crushed with a pulverizer and sifted through a 100-mesh sieve yielding RBC particles having a mean particle size in the range of 240 to 260 ⁇ m.
  • RBC particles in the amount of 75 kilograms and 50 kilograms of a solid phenolic resin (resol) were mixed and kneaded while being heated at 50-60° C. A plastic mixture of uniform quality was obtained.
  • the plastic mixture was molded under a pressure of 22 Mpa into a globular shape whose diameter was approximately 1 centimeter.
  • the temperature of the metal mold was 150° C.
  • the molded product was taken out of the metal mold, and the temperature was elevated at a rate of 2° C. per minute, until 500° C. was reached. The temperature was held for 60 minutes at 500° C., and then firing was carried out at 900° C. for approximately 120 minutes.
  • the resulting CRBC product was crushed with a pulverizer and, by using a 170-mesh sieve, CRBC particles having a mean particle size of from 145 to 155 ⁇ m were obtained.
  • CRBC particles in the amount of 600 grams and 400 grams of polyamide (nylon 11) pellets were mixed and kneaded while being heated at 190-200° C. A plastic mixture of uniform quality was obtained.
  • the mixture was fired at 950° C. in a rotary kiln for 120 minutes in a nitrogen atmosphere.
  • the resulting carbonized product was pulverized and then sifted through a 100-mesh sieve to yield RBC particles having a mean particle size of from about 240 to 260 ⁇ m.
  • the plastic product was molded under a pressure of 22 Mpa into a globular shape whose diameter was approximately 1 centimeter.
  • the temperature of the metal mold was 150° C.
  • the molded product was taken out of the metal mold. The temperature was then raised in a nitrogen atmosphere at the rate of 3° C. per minute until 500° C. was achieved. It was held at 500° C. for 30 minutes; and then fired for approximately 120 minutes at 1000° C.
  • the resulting CRBC product was pulverized and subjected to a 170-mesh sieve yielding CRBC particles having a mean particle size of 145 to 155 ⁇ m.
  • CRBC particles in the amount of 600 grams, having a mean particle size of 150 ⁇ m, and 400 grams of polybutylene terephthalate powder were mixed and kneaded while being heated at 240-260° C. A plastic mixture of uniform quality was obtained.
  • CRBC particles in the amount of 700 grams from Example 8 (having a mean particle size of 150 ⁇ m) and 300 grams of polypropylene particles were mixed and kneaded while being heated at 190-210° C. A plastic mixture of uniform quality was obtained.

Landscapes

  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Medicinal Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Ceramic Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Sliding-Contact Bearings (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

A low noise composition includes fine particles of RBC or CRBC dispersed in a synthetic resin. The composition can be formed into an article of manufacture prepared by molding the composition.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention [0001]
  • The present invention relates to synthetic resin compositions. More particularly, the present invention relates to synthetic resin compositions that can be molded into articles that generate less noise in use. [0002]
  • 2. Description of the Related Art [0003]
  • In the fields of office automation (“OA”) machines, automobile parts, and machinery, there has been progress in the use of resin for parts such as wheels, cams, and bearings by employing engineering plastics, such as polyacetal and the like. The use of these resins has greatly contributed to reducing the manufacturing costs of articles produced from them. [0004]
  • Unfortunately, in many cases, particularly where the molded parts are required to slide against other parts during use, noise is generated. Attempts have been made to reduce this high noise level by reducing the modulus of elasticity of the resin itself, for example, by applying grease to the resin. This solution, however, has been unsatisfactory. It has been found that the applied grease can, in use, spatter to the surrounding mechanisms, adversely affecting their physical properties. In addition, other problems may arise, such as an increase in torque, a reduction in strength, and a general lowering of efficiency. [0005]
  • Another cause of noise in engineering plastics is the “stick-slip phenomenon.”When one surface is pressed against another surface with a normal force, n, and another force is applied that causes the one surface to slide across another surface, a drag force can be measured that is parallel to the surfaces and in a direction opposite to the applied force. This kinetic drag force, f[0006] k, is called a dynamic friction force or kinetic friction force and is related to the magnitude of the normal force by a dynamic friction coefficient, μD(vs). The dynamic friction coefficient, μD(vs), depends upon the sliding speed, vs, and the surface characteristics of each of the materials in contact with each other. If μD is known for a particular vs, then the dynamic friction coefficient is determined by the following formula: fkD·n, where fk is the dynamic friction force and n is the normal force pressing the surfaces together. Thus, μD may be measured by determining the ratio fk/n.
  • Generally, the dynamic friction force and the coefficient of dynamic friction approach a constant value as the sliding speed, v[0007] s, approaches a high velocity, for example greater than 1 meter per second (m/s). Thus, at high velocities the coefficient of dynamic friction is independent of the sliding speed, vs. However, at low sliding speed, vs, the coefficient of dynamic friction, μD, is speed dependent. Typically, the dynamic friction force, fk, approaches a maximum as the sliding speed, vs, approaches 0. When the sliding speed, vs, is 0, then the two surfaces are at rest with each other, and the measured friction force is defined as a static friction force. The maximum static friction force, fmax, occurs immediately prior to the onset of sliding. A large difference between the maximum static friction force, fmax, at vs=0 and the dynamic static force at a high sliding speed, fk(vs=∞), results in stick-slip behavior. A large difference between fmax and fk(v2=∞) results in stick-slip behavior that causes excessive noise in mechanical devices that use the material. Thus, it is desirable to have a material with little or no stick-slip behavior.
  • The stick-slip phenomenon may be understood by a perusal of FIGS. 1 and 2 which show a device used for placing a certain load W at a [0008] tip 2′ of a stick 2. Stick 2 is held by a bearing 4 in a freely rotatable fashion on a disc 1 made of the testing material. A spring 3 is fixed at the intermediate part of stick 2. Disk 1 is rotated in the direction indicated by the arrow mark by means of a driving device 5.
  • When the rotation of [0009] disk 1 is started by driving device 5, stick 2 shifts from its static position A0 to A1 where a balance is struck with spring 3, thereby achieving a stable state because of the difference between the static friction coefficient μS and the dynamic friction coefficient μD on the contact surface between disk 1 and tip 2′ of stick 2. Where the difference between the static friction coefficient μS and the dynamic friction coefficient μD is large, a strain greater than the normal value is applied to spring 3, whereupon A1 is exceeded and A2 is reached. The stick is then displaced to position A−1 and brought back to A0 by the restorative force of the spring.
  • If, in this state, [0010] disk 1 is caused to continue rotating, stick 2 will repeat the same action between A−1, A0, and A2. As a consequence, the stick will start vibrating, thereby generating noise.
  • Thus, the stick-slip phenomenon is created by the difference between the static friction coefficient μ[0011] S and the dynamic friction coefficient μD. When a resin composition having a large difference is molded into a machine element, the stick slip phenomenon is manifested as noise in a machine device using the machine element.
  • Thus, there is a need for a resin composition that can be molded into useful parts that inherently will produce little or no noise in use. [0012]
  • SUMMARY OF THE INVENTION
  • The present invention relates to a synthetic resin composition for preventing noise in finished parts molded from the composition. The materials have a small difference between their static friction coefficient, μ[0013] S, and their dynamic friction coefficient, μD. This substantially reduces the “stick-slip phenomenon”, which is the source of noise in engineering plastics, such as polyacetal and the like.
  • More particularly, the present invention is directed to a low noise composition comprising fine particles of RBC or CRBC uniformly dispersed in a synthetic resin. [0014]
  • In an alternative embodiment, the present invention is directed to an article of manufacture comprising a molded low noise synthetic resin composition comprising fine particles of RBC or CRBC uniformly dispersed in a synthetic resin. [0015]
  • Other features and advantages of the present invention will become apparent from the following description of the preferred embodiments.[0016]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is an oblique view of the equipment for measuring the stick-slip phenomenon. [0017]
  • FIG. 2 is a cross section of the equipment for measuring the stick-slip phenomenon. [0018]
  • FIG. 3 is a graph depicting the friction characteristics of a polyacetal molded product (“RBC/POM”). [0019]
  • FIG. 4 is a graph depicting the friction characteristics of a polyamide (nylon 66) molded product (“RBC/PA66”). [0020]
  • FIG. 5 is a graph depicting the friction characteristics of a polyamide (nylon 66) molded product containing glass fibers (“RBC/GF23PA66”). [0021]
  • FIG. 6 is a graph depicting the friction characteristics of a polyamide (nylon 11) molded product (“CRBC/PA11”). [0022]
  • FIG. 7 is a graph depicting the friction characteristics of a polybutylene terephthalate molded product (“CRBC/PBT”). [0023]
  • FIG. 8 is a graph depicting the friction characteristics of a polypropylene molded product (“CRBC/PP”). [0024]
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • In accordance with the present invention, fine particles of a rice bran ceramic (“RBC”) or a carbonized rice bran ceramic (“CRBC”) are uniformly dispersed in a synthetic resin to provide a low noise composition. RBC and CRBC are advantageous because they possess the following qualities: [0025]
  • 1. they are very hard; [0026]
  • 2. when they are made into grains, their shape is irregular; [0027]
  • 3. their expansion coefficient is extremely small; [0028]
  • 4. they are electrically conductive; [0029]
  • 5. their specific gravity is low and they are light and porous; [0030]
  • 6. their friction coefficient is extremely small; and [0031]
  • 7. their resistance to friction is superior. [0032]
  • Moreover, because the materials are rice bran, there is no adverse effect upon the earth's environment and they serve to preserve natural resources. [0033]
  • To produce RBC or CRBC, rice bran is preferably used as a starting material because of its low cost. Large quantities are produced as a by-product of other processes, e.g., about 900,000 tons per year in Japan alone and 33,000,000 tons per year throughout the world. [0034]
  • RBC is a carbon material made, for example, by mixing and kneading a de-fatted rice bran (de-fatted bran obtained from rice) with a thermally hardening or thermosetting resin, molding a product from the mixture, drying it, and then firing the dried molded product in an inert gas atmosphere, e.g., sintering. See Kazuo Hokkirigawa, Kino Zairyo “Functional Materials”, Vol. 17, No. 5, pp. 24-28 (May 1997). [0035]
  • Preferably, the thermosetting resin that is mixed with the de-fatted rice bran should be any resin that is heat hardened or cured by heating. Preferred resins include, but not limited to, phenolics, diaryl phthalate resins, unsaturated polyester resins, epoxies, polyimides, triazine resins and the like. Phenolic resins, e.g., resols, are especially preferred. [0036]
  • The mixing ratio of de-fatted rice bran to the thermosetting resin should be in the range from about 50 to 90:50 to 10 (about 50:50 to about 90:10) by weight. A ratio of about 75:25 is especially preferred. [0037]
  • CRBC is a carbon material also obtained from defatted rice bran and a thermosetting resin, bus is an improvement over RBC. To prepare a CRBC, for example, the de-fatted rice bran and the thermosetting resin are mixed, kneaded, and then first fired in an inert gas atmosphere at a temperature in the range of about 700° C. to 1000° C., e.g., sintered. Ordinarily, the mixture is fired in a rotary kiln for a period of about 40 to about 120 minutes. The resulting material is then pulverized (crushed) into to less than about 100 mesh to form carbonized powder. [0038]
  • The carbonized powder is then mixed with a thermosetting resin, which may be, but is not necessarily, the same as that employed with the de-fatted rice bran, and kneaded. This product is then molded under pressure in the range of about 20 Mpa to 30 Mpa. The molded product is once again heat treated in an inert gas atmosphere at a temperature in the range from about 100° to 1100° C., e.g., sintered, thereby obtaining a black resin or porous CRBC ceramic. [0039]
  • According to the present invention, fine particles of RBC or CRBC are mixed with a synthetic resin to form a synthetic resin composite having unique and useful friction characteristics. Preferably, the RBC or CRBC constitutes about 30-70% by weight of the entire synthetic resin composite. Preferably, the weight ratio of the RBC or CRBC particles to the synthetic resin is about 30 to 90:70 to 10 (about 30:70 to about 90:10). [0040]
  • In a preferred embodiment, the RBC or CRBC particles are uniformly dispersed in a synthetic resin. The fine particles are uniformly dispersed by mixing them with the synthetic resin at or near the resin's fusion point, followed by kneading. As a result of the uniform dispersal, and especially when the weight ratio of the particles to the synthetic resin is about 30 to 90:70 to 10 (about 30:70 to about 90:10), the difference between the static friction coefficient μ[0041] S and the dynamic friction coefficient μD on the surface of an article molded from the composition is reduced.
  • In a preferred embodiment, the RBC or CRBC should have a mean particle size of about 300 μm or less, preferably a mean particle size of about 20-150 μm. It has been found that a synthetic resin composite of the present invention including fine particles of RBC or CRBC, results in a composition that has surface characteristics that make the composition particularly suitable for use in low noise applications. [0042]
  • Preferably, the synthetic resins that are mixed with the RBC or CRBC are thermoplastic resins. Examples of these resins include, but are not limited to, polyacetal, polyamide, polyester, polyolefins, and the like. POM (polyacetal, i.e., polyoxymethylene), nylon 66 (polyhexamethylene adipamide), nylon 6 (polycapramide), nylon 11 (polyundecanamide), nylon 12, polybutylene terephthalate, polyethylene teraphthalate, polypropylene, polyethylene, and other thermoplastic resins are preferred. Among these, POM, nylon 66, nylon 11, polybutylene terephthalate, polypropylene, and the like are more preferred. These thermoplastic resins can be used either alone or in combination. [0043]
  • The thermoplastic resin or resins can be used in combination with one or more thermosetting resins. As stated above, the thermosetting resins that can be used in the present invention include, but are not limited to, phenolics, diaryl phthalate resins, unsaturated polyester resins, epoxies, polyimides, triazine resins system, and the like. [0044]
  • In a preferred embodiment, the RBC or CRBC should constitute about 30-70% by weight of the synthetic composition. For example, the weight ratio of the fine particles of RBC or CRBC to the synthetic resin should be about 30 to 90:70 to 10. It has been found that if the synthetic resin exceeds about 70 weight percent, the difference between the static friction coefficient μ[0045] S and the dynamic friction coefficient μD becomes too large. On the other hand, if it is less than about 10 weight percent, molding becomes difficult.
  • The low noise synthetic resin composition of the present invention can be molded into any given shape by any of the known methods. Preferably, the molded compositions are used in the manufacture of machine elements, such as, for example, screws, bearings, axial relays, cam mechanisms, cylinders and pistons, wheels, belts and pulleys, chains and sprockets, valves and tubes, and the like. [0046]
  • Preferably, molding is carried out by extrusion molding, injection molding or by any of the known methods. Preferably, the temperature of the mold should be relatively low, preferably in the range between the glass transition point of the synthetic resin and its fusion point. It is also preferred that the mold be cooled gradually rather than suddenly, which will normally provide a molded product having superior surface conditions. [0047]
  • In a preferred embodiment, the strength of the molded product can be increased by adding inorganic fibers, such as glass fiber, rock wool, carbon fibers, and the like; synthetic fibers, such as polyester, rayon, polyvinyl alcohol, polyamide, polyolefin, acrylic, and the like; or natural pulp fibers, such as wood pulp, Manila hemp, and the like. [0048]
  • The advantages and the important features of the present invention will become more apparent from Examples 1-9 set forth below and FIGS. [0049] 3-8.
  • EXAMPLES
  • Examples 1-9 include materials made with and without RBC or CRBC as an additive. The friction characteristics of each of the examples was then measured, and the examples without RBC or CRBC as additives were compared to examples with RBC or CRBC as an additive. [0050]
  • FIGS. [0051] 3-8 each show the dynamic friction coefficient, μD versus the slide speed, vs, for Examples 1-9 (materials with and without RBC or CRBC particulate additives). Measurements were made of the dynamic coefficient of friction, μD, over a range of sliding speeds, vs, from 0.001 m/s to 1.0 m/s for various materials, e.g., in the range of 0.001-0.01 m/s and 0.1-1 m/s. A normal force, n, of 0.49 Newtons (N) was applied, pressing a SUJ ball with a diameter of 2 millimeters (mm) into contact with the surface of a specimen.
  • A reciprocating friction test apparatus was used to measure the dynamic friction force for sliding speeds in the range from 0.001 m/s to 0.01 m/s, and a rotary friction test apparatus was used to measure the dynamic friction force, f[0052] k, at higher velocities from 0.1 m/s to 1 m/s. In the case of the reciprocating friction test, the reciprocating arm repeated 1000 strokes and the stroke distance was 5 mm, which was a distance sufficient to reach a steady measurement of the dynamic friction force, fk, which was used to calculate μD.
  • As shown below, the specimens were prepared by injecting heated materials into a metal mould to produce a circular specimen with a diameter of 50 mm and a thickness of 3 mm. The injection temperature varied, depending on the compositions of the materials used in each of the examples, as noted below. An ester lubricating oil was applied to surface of the material prior to each test. [0053]
  • FIGS. [0054] 3-8 demonstrate that the materials without RBC or CRBC particulate additives show stick-slip behavior, and the materials with RBC or CRBC particulate additives show little or no stick-slip behavior. Instead, materials with RBC or CRBC particulate additives show a nearly constant dynamic friction coefficient, μD, over the full range of slide speeds tested, even at sliding speeds as low as 0.001 m/s. Thus, the specific examples described below indicate that materials with RBC or CRBC particulate additives reduce stick-slip behavior, avoiding the generation of noise.
  • Example 1
  • Preparation of RBC Fine Particles [0055]
  • De-fatted rice bran in the amount of 75 kilograms and 25 kilograms of phenolic resin (resol) were mixed and kneaded while being heated at a temperature of 50-60° C. A plastic mixture of uniform quality, i.e., a homogenous mixture, was obtained. [0056]
  • The mixture was fired in a rotary kiln for 120 minutes at 900° C. in a nitrogen atmosphere. The resulting carbonized product was sifted through a 170-mesh sieve. Fine RBC particles having a mean particle size in the range of 145 to 155 μm were obtained. [0057]
  • Preparation of Mixture of RBC Fine Particles and Synthetic Resin [0058]
  • RBC fine particles in the amount of 500 grams (having a mean particle size of 150 μm) and 500 grams of polyacetal resin (POM) pellets were mixed and kneaded, while being heated at a temperature of 180-230° C. A plastic mixture of uniform quality was obtained. [0059]
  • Molding of Test Pieces [0060]
  • The above resin composition, heated at a temperature of 190° C., was injected into a metal mold (in the range between 115° C. and 135° C.) to produce [0061] test pieces 3 millimeters thick and 50 millimeters in diameter.
  • Measurement of Friction Characteristics [0062]
  • The results are shown in FIG. 3. [0063]
  • Example 2
  • Preparation of Fine RBC Particles [0064]
  • De-fatted rice bran in the amount of 75 kilograms and 25 kilograms of a liquid phenolic resin (resol) were mixed and kneaded while being heated at 50-60° C. A plastic mixture having uniform quality was obtained. [0065]
  • The mixture was fired at 1,000° C. for 120 minutes in a rotary kiln in a nitrogen atmosphere. The resulting carbonized product was sifted through a 170-mesh sieve yielding RBC particles having a mean particle size in the range of from 145 to 155 μm. [0066]
  • Preparation of Mixture of Fine RBC Particles and Synthetic Resin [0067]
  • RBC particles in the amount of 200 grams (whose mean particle diameter was 150 μm) and 800 grams of polyacetal resin (POM) pellets were mixed and kneaded while being heated at 180-200° C. A plastic mixture of uniform quality was obtained. [0068]
  • Preparation of Test Pieces [0069]
  • The above resin composition, heated at a temperature of 190° C., was injected into a metal mold (115 to 135° C.) to produce [0070] test pieces 3 millimeters thick and 50 millimeters in diameter.
  • Measurement of Friction Characteristics [0071]
  • The results are shown in FIG. 3. [0072]
  • Example 3
  • Preparation of Fine RBC Particles [0073]
  • De-fatted rice bran in the amount of 75 kilograms and 25 kilograms of a liquid phenolic resin (resol) were mixed and kneaded while being heated at 50-60° C. A plastic mixture of uniform quality was obtained. [0074]
  • The mixture was fired at 900° C. for 120 minutes in a rotary kiln in a nitrogen atmosphere. The resulting carbonized product was pulverized and sifted through an 800-mesh sieve yielding RBC particles having a mean particle size of 30 μm. [0075]
  • Preparation of Mixture of Fine RBC Particles and Synthetic Resin [0076]
  • The above RBC particles in the amount of 500 grams and 500 grams of polyamide (nylon 66) pellets were mixed and kneaded while being heated at 260-280° C. A plastic mixture of uniform quality was obtained. [0077]
  • Molding of Test Pieces [0078]
  • The above resin composition, heated at a temperature of 270° C., was injected into a metal mold (130-150° C.) to produce [0079] test pieces 3 millimeters thick and 50 millimeters in diameter.
  • Measurement of Friction Characteristics [0080]
  • The results are shown in FIG. 4. [0081]
  • Example 4
  • Preparation of a Mixture of Fine RBC Particles and Synthetic Resin [0082]
  • RBC particles in the amount of 300 grams obtained in Example 3 having a mean particle size of about 150 μm and 700 grams of polyamide (nylon 66) pellets were mixed and kneaded while being heated at 260-280° C. [0083]
  • Molding of Test Pieces [0084]
  • The above resin composition, heated at 270° C., was injected into a metal mold (110-130° C.) to produce [0085] test pieces 3 millimeters thick and 50 millimeters in diameter.
  • Measurement of Friction Characteristics [0086]
  • The results are shown in FIG. 4. [0087]
  • Example 5
  • Preparation of Mixture of RBC Fine Particles and Synthetic Resin [0088]
  • RBC particles from Example 1 in the amount of 300 grams having a mean particle size of 150 μm, and 700 grams of polyamide (nylon 66) pellets were mixed and kneaded while being heated at 260-280° C. A plastic mixture of uniform quality was obtained. [0089]
  • Molding of Test Pieces [0090]
  • The above resin composition, heated at a temperature of 270° C., was injected into a metal mold (130-140° C.) to produce a [0091] test piece 3 millimeters thick and 50 millimeters in diameter.
  • Measurement of Friction Characteristics [0092]
  • The results are shown in FIG. 4. [0093]
  • Example 6
  • Preparation of Mixture of Fine RBC Particles and Synthetic Resin [0094]
  • RBC particles from Example 2 in the amount of 300 grams having a mean particle size of 150 μm, and 700 grams of polyamide (nylon 66) pellets were mixed and kneaded while being heated at 260-280° C. As a result, a plastic mixture of uniform quality was obtained. [0095]
  • Next, 100 grams of glass fiber were mixed in. The mixing was continued for a sufficient time until uniformity was obtained. [0096]
  • Molding of Test Pieces [0097]
  • The above resin composition, heated at a temperature of 270° C., was injected into a metal mold (130-140° C.) to produce [0098] test pieces 3 millimeters thick and 50 millimeters in diameter.
  • Measurement of Friction Characteristics [0099]
  • The results are shown in FIG. 5. [0100]
  • Example 7
  • Preparation of Fine CRBC Particles [0101]
  • De-fatted rice bran in the amount of 75 kilograms and 25 kilograms of liquid phenolic resin (resol) were mixed and kneaded at 50-60° C. A plastic mixture of uniform quality was obtained. [0102]
  • The mixture was fired at 900° C. for 100 minutes in a rotary kiln in a nitrogen atmosphere. The resulting carbonized product was crushed with a pulverizer and sifted through a 100-mesh sieve yielding RBC particles having a mean particle size in the range of 240 to 260 μm. [0103]
  • RBC particles in the amount of 75 kilograms and 50 kilograms of a solid phenolic resin (resol) were mixed and kneaded while being heated at 50-60° C. A plastic mixture of uniform quality was obtained. [0104]
  • Next, the plastic mixture was molded under a pressure of 22 Mpa into a globular shape whose diameter was approximately 1 centimeter. The temperature of the metal mold was 150° C. [0105]
  • The molded product was taken out of the metal mold, and the temperature was elevated at a rate of 2° C. per minute, until 500° C. was reached. The temperature was held for 60 minutes at 500° C., and then firing was carried out at 900° C. for approximately 120 minutes. [0106]
  • Next, the temperature was lowered at a cooling rate of 2 to 3° C. per minute until 500° C. was reached. Below 500° C., it was left to cool naturally. [0107]
  • The resulting CRBC product was crushed with a pulverizer and, by using a 170-mesh sieve, CRBC particles having a mean particle size of from 145 to 155 μm were obtained. [0108]
  • Preparation of Mixture of Fine CRBC Particles and Synthetic Resin [0109]
  • CRBC particles in the amount of 600 grams and 400 grams of polyamide (nylon 11) pellets were mixed and kneaded while being heated at 190-200° C. A plastic mixture of uniform quality was obtained. [0110]
  • Molding of Test Pieces [0111]
  • The above resin composition, heated at a temperature of 200° C., was injected into a metal mold (90-110° C.) to produce test pieces three millimeters thick and 50 millimeters in diameter. [0112]
  • Measurement of the Friction Characteristics [0113]
  • The results are shown in FIG. 6. [0114]
  • Example 8
  • Preparation of Fine CRBC Particles [0115]
  • De-fatted rice bran in the amount of 75 kilograms and 25 kilograms of a liquid phenolic resin (resol) were mixed and kneaded while being heated at 50-60° C. A plastic mixture of uniform quality was obtained. [0116]
  • The mixture was fired at 950° C. in a rotary kiln for 120 minutes in a nitrogen atmosphere. The resulting carbonized product was pulverized and then sifted through a 100-mesh sieve to yield RBC particles having a mean particle size of from about 240 to 260 μm. [0117]
  • RBC particles in the amount of 75 kilograms and 35 kilograms of a solid phenolic resin (resol) were mixed and kneaded while being heated at 50-60° C. A plastic mixture of uniform quality was obtained. [0118]
  • Next, the plastic product was molded under a pressure of 22 Mpa into a globular shape whose diameter was approximately 1 centimeter. The temperature of the metal mold was 150° C. [0119]
  • The molded product was taken out of the metal mold. The temperature was then raised in a nitrogen atmosphere at the rate of 3° C. per minute until 500° C. was achieved. It was held at 500° C. for 30 minutes; and then fired for approximately 120 minutes at 1000° C. [0120]
  • Next, the temperature was lowered at a cooling rate of 2 to 3° C. per minute until 500° C. was reached, then left to cool naturally. [0121]
  • The resulting CRBC product was pulverized and subjected to a 170-mesh sieve yielding CRBC particles having a mean particle size of 145 to 155 μm. [0122]
  • Preparation of Mixture of Fine CRBC Particles and Synthetic Resin [0123]
  • CRBC particles in the amount of 600 grams, having a mean particle size of 150 μm, and 400 grams of polybutylene terephthalate powder were mixed and kneaded while being heated at 240-260° C. A plastic mixture of uniform quality was obtained. [0124]
  • Molding of Test Pieces [0125]
  • The above resin composition, heated at a temperature of 260° C., was injected into a metal mold (80-100° C.) to produce [0126] test pieces 3 millimeters thick and 50 millimeters in diameter.
  • Measurement of Friction Characteristics [0127]
  • The results are shown in FIG. 7. [0128]
  • Example 9
  • Preparation of Mixture of Fine CRBC Particles and Synthetic Resin [0129]
  • CRBC particles in the amount of 700 grams from Example 8 (having a mean particle size of 150 μm) and 300 grams of polypropylene particles were mixed and kneaded while being heated at 190-210° C. A plastic mixture of uniform quality was obtained. [0130]
  • Molding of Test Pieces [0131]
  • The above resin composition, heated at a temperature of 220° C., was injected into a metal mold (80-90° C.) to produce [0132] test pieces 5 millimeters thick and 50 millimeters in diameter.
  • Measurement of Friction Characteristics [0133]
  • The results are shown in FIG. 8. [0134]
  • The results from FIGS. [0135] 3-8 clearly show that the synthetic resin composition that contains fine particles of RBC or CRBC of the present invention is a material in which the difference between the static friction coefficient μS and dynamic friction coefficient μD is small. As a result, the stick-slip phenomenon is significantly reduced, thereby allowing the composition of the present invention to have a wide range of uses for various kinds of machinery elements.
  • Although the present invention has been described in relation to particular embodiments thereof, many other variations and modifications and other uses will become apparent to those skilled in the art. The present invention therefore is not limited by the specific disclosure herein. [0136]

Claims (44)

What is claimed is:
1. An article of manufacture, comprising:
a molded low noise resin composition including particles of at least one of RBC and CRBC dispersed in a resin.
2. The article of manufacture of claim 1, wherein the particles are uniformly dispersed in the resin.
3. The article of manufacture of claim 1, wherein the composition includes about 30-70% by weight of the at least one of RBC and CRBC.
4. The article of manufacture of claim 1, wherein the weight ratio of the fine particles of the at least one of RBC and CRBC to the resin is about 30 to 90:70 to 10.
5. The article of manufacture of claim 1, wherein the particles include a powder.
6. The article of manufacture of claim 1, wherein the resin is a thermoplastic resin selected from the group consisting of at least one of: polyacetal, polyamide, polyester, and polyolefins.
7. The article of manufacture of claim 6, wherein the thermoplastic resin is selected from the group consisting of at least one of: polyacetal, nylon 66, nylon 6, nylon 11, nylon 12, polybutylene terephthalate, polyethylene terephthalate, polypropylene, and polyethylene.
8. The article of manufacture of claim 1, wherein the mean particle size of the particles of the at least one of RBC and CRBC is about 300 μm or less.
9. The article of manufacture of claim 7, wherein the mean particle size of the particles of the at least one of RBC and CRBC is about 20 to 150 μm.
10. The article of manufacture of claim 1, further comprising fibers selected from the group consisting of at least one of: inorganic fibers, synthetic fibers, and natural pulp fibers.
11. The article of manufacture of claim 1, wherein the article is molded into a form selected from the group consisting of at least one of: screws, axial relays, cam mechanisms, cylinders, pistons, wheels, friction wheels, belts, pulleys, chains, sprockets, valves, and tubes.
12. An article of manufacture, comprising:
a body having a low friction contact surface, at least part of the body being formed from a composite material including,
fine particles of at least one of RBC and CRBC; and
a resin material, wherein the fine particles are dispersed within the resin material.
13. The article of manufacture of claim 12, wherein the fine particles are uniformly dispersed in the resin material.
14. The article of manufacture of claim 12, wherein the body includes at least one of a screw, an axial relay, a cam mechanism, a cylinder, a piston, a wheel, a friction wheel, a belt, a pulley, a chain, a sprocket, a valve, and a tube.
15. The article of manufacture of claim 12, wherein the composite material includes about 30-70% by weight of the at least one of RBC and CRBC.
16. The article of manufacture of claim 12, wherein the weight ratio of the fine particles to the resin material is about 30 to 90:70 to 10.
17. The article of manufacture of claim 12, wherein the resin material is a thermoplastic resin.
18. The article of manufacture of claim 17, wherein the resin is selected from the group consisting of at least one of: polyacetal, polyamide, polyester, polyolefins.
19. The article of manufacture of claim 18, wherein the resin is selected from the group consisting of at least one of: polyacetal, nylon 66, nylon 6, nylon 11, nylon 12, polybutylene terephthalate, polyethylene terephthalate, polypropylene, and polyethylene.
20. The article of manufacture of claim 12, wherein the mean particle size of the fine particles is about 300 μm or less.
21. The article of manufacture of claim 20, wherein the mean particle size of the fine particles is about 20 to 150 μm.
22. The article of manufacture of claim 12, further comprising fibers selected from the group consisting of at least one of: inorganic fibers, synthetic fibers, and natural pulp fibers.
23. The article of manufacture of claim 22, wherein the synthetic fibers are selected from the group consisting of at least one of: polyester, rayon, polyvinyl alcohol, polyamide, polyolefin and acrylic.
24. The article of manufacture of claim 22, wherein the natural pulp fibers are selected from the group consisting of: wood pulp and Manila hemp.
25. The article of manufacture of claim 17, wherein the resin material includes a thermosetting resin.
26. The article of manufacture of claim 25, wherein the thermosetting resin is selected from the group consisting of at least one of: phenolics, diaryl phthalate resins, unsaturated polyester resins, epoxies, polyimides, and a triazine resins system.
27. An apparatus, comprising:
a component, wherein the component has a low noise contact surface, and at least part of the component is formed of a composite including a resin and about 30-70% by weight of at least one of RBC and CRBC, wherein the at least one of RBC and CRBC is uniformly dispersed in the resin.
28. The apparatus of claim 27, wherein the mean particle size of the at least one of RBC and CRBC is about 300 μm or less.
29. The apparatus of claim 28, wherein the mean particle size is about 20 to 150 μm.
30. The apparatus of claim 27, wherein the component is at least one of a screw, an axial relay, a cam mechanism, a cylinder, a piston, a wheel, a friction wheel, a belt, a pulley, a chain, a sprocket, a valve, and a tube.
31. A method for manufacturing low noise machinery parts, comprising the steps of:
a) providing fine particles of at least one of RBC and CRBC;
b) providing at least one resin material;
c) mixing the fine particles with the at least one resin material to obtain a mixture; and
d) forming at least one part of an article from the mixture, wherein the at least part of the article includes a composite material having the fine particles dispersed within the resin material.
32. The method of claim 31, wherein the mixture is heated before forming the article.
33. The method of claim 31, wherein the article is formed by molding.
34. The method of claim 31, wherein the article is formed by one of extrusion molding and injection molding.
35. The method of claim 31, wherein the molding takes place at a temperature between the glass transition temperature and the melting temperature of the at least one resin material.
36. The method of claim 31, further comprising the step of: cooling the article gradually.
37. The method of claim 31, wherein the fine particles are uniformly dispersed within the at least one resin material.
38. The method of claim 31, wherein the article is one of a screw, an axial relay, a cam mechanism, a cylinder, a piston, a wheel, a friction wheel, a belt, a pulley, a chain, a sprocket, a valve, and a tube.
39. The method of claim 31, wherein the weight ratio of the fine particles to the resin material is about 30 to 90:70 to 10.
40. The method of claim 31, wherein the resin material is a thermoplastic resin.
41. The method of claim 40, wherein the resin is selected from the group consisting of at least one of: polyacetal, nylon 66, nylon 6, nylon 11, nylon 12, polybutylene terephthalate, polyethylene terephthalate, polypropylene, and polyethylene.
42. The method of claim 31, wherein the mean particle size of the fine particles is about 300 μm or less.
43. The method of claim 42, wherein the mean particle size of the fine particles is about 20 to 150 μm.
44. The method of claim 31, further comprising the step of: adding at least fiber selected from the group consisting of at least one of: inorganic fibers, synthetic fibers, and natural pulp fibers to the mixture of the fine particles and the resin material.
US10/377,964 2002-03-01 2003-02-28 Low noise synthetic resin composition and method Abandoned US20030220421A1 (en)

Applications Claiming Priority (12)

Application Number Priority Date Filing Date Title
JP2002055307 2002-03-01
JP2002-055307 2002-03-01
JP2002-055308 2002-03-01
JP2002055308A JP2003253132A (en) 2002-03-01 2002-03-01 Low-friction high-dispersion synthetic resin composition containing fine powder of rbc or crbc, and its production process
JP2002-062406 2002-03-07
JP2002062406A JP4031266B2 (en) 2002-03-07 2002-03-07 Underwater sliding resin composition containing fine powder of RBC or CRBC
JP2002-062412 2002-03-07
JP2002062412A JP2003263923A (en) 2002-03-07 2002-03-07 Black conductive synthetic resin composition containing fine powder of rbc or crbc and its manufacturing method
JP2002176436A JP2004018700A (en) 2002-06-17 2002-06-17 Synthetic resin composition for low noise and application thereof
JP2002-176436 2002-06-17
JP2002-272147 2002-09-18
JP2002272147A JP2004108499A (en) 2002-09-18 2002-09-18 Synthetic resin compound for sliding bearings and sliding bearing molding the same

Publications (1)

Publication Number Publication Date
US20030220421A1 true US20030220421A1 (en) 2003-11-27

Family

ID=27767965

Family Applications (6)

Application Number Title Priority Date Filing Date
US10/377,964 Abandoned US20030220421A1 (en) 2002-03-01 2003-02-28 Low noise synthetic resin composition and method
US10/376,580 Expired - Fee Related US6787075B2 (en) 2002-03-01 2003-02-28 Method of making synthetic resin composition with lubricative underwater properties containing RBC or CRBC fine powder
US10/377,849 Expired - Fee Related US7144932B2 (en) 2002-03-01 2003-02-28 Low-friction, high-dispersion synthetic resin composition containing fine particles of RB ceramic or CRB ceramic and a method for its preparation
US10/376,419 Abandoned US20030179963A1 (en) 2002-03-01 2003-02-28 Low friction sleeve bearing
US10/377,851 Expired - Fee Related US7140778B2 (en) 2002-03-01 2003-02-28 Synthetic resin composites and bearings formed therefrom and method
US10/931,707 Abandoned US20050032939A1 (en) 2002-03-01 2004-08-28 Synthetic resin composition with lubricative underwater properties containing RBC or CRBC fine powder

Family Applications After (5)

Application Number Title Priority Date Filing Date
US10/376,580 Expired - Fee Related US6787075B2 (en) 2002-03-01 2003-02-28 Method of making synthetic resin composition with lubricative underwater properties containing RBC or CRBC fine powder
US10/377,849 Expired - Fee Related US7144932B2 (en) 2002-03-01 2003-02-28 Low-friction, high-dispersion synthetic resin composition containing fine particles of RB ceramic or CRB ceramic and a method for its preparation
US10/376,419 Abandoned US20030179963A1 (en) 2002-03-01 2003-02-28 Low friction sleeve bearing
US10/377,851 Expired - Fee Related US7140778B2 (en) 2002-03-01 2003-02-28 Synthetic resin composites and bearings formed therefrom and method
US10/931,707 Abandoned US20050032939A1 (en) 2002-03-01 2004-08-28 Synthetic resin composition with lubricative underwater properties containing RBC or CRBC fine powder

Country Status (3)

Country Link
US (6) US20030220421A1 (en)
EP (2) EP1347009A1 (en)
CN (3) CN1453310A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030179963A1 (en) * 2002-03-01 2003-09-25 Minebea Co., Ltd. Low friction sleeve bearing
US20030210995A1 (en) * 2002-03-13 2003-11-13 Minebea Co., Ltd. Electrically motorized pump for use in water
US20040031642A1 (en) * 2002-06-05 2004-02-19 Kazuo Hokkirigawa Air purifying sound insulating wall and its applications
US20040132881A1 (en) * 2003-01-07 2004-07-08 Minebea Co., Ltd. Oil repelling agent
US20040258334A1 (en) * 2003-02-28 2004-12-23 Minebea Co., Ltd. Underwater sleeve bearing and application thereof
US6887288B2 (en) 2002-06-05 2005-05-03 Minebea Co., Ltd. Superfinishing grindstone
US7008196B2 (en) 2003-03-11 2006-03-07 Minebea Co. Ltd. Electrically motorized pump having a submersible sleeve bearing
US9120913B2 (en) 2013-09-30 2015-09-01 Hitachi Metals, Ltd. Elastic composite material and mold product using the same
CN105238043A (en) * 2015-11-09 2016-01-13 安徽省宁国顺昌机械有限公司 Isolating block for slewing bearing

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004019368A (en) 2002-06-19 2004-01-22 Minebea Co Ltd Road paving material
JP3422994B1 (en) 2002-10-17 2003-07-07 ジューキ株式会社 Lubricants, sliding members and solid lubricants
EP1518891A1 (en) * 2003-09-18 2005-03-30 Minebea Co., Ltd. Synthetic resin and bearing parts made thereform
US7128061B2 (en) * 2003-10-31 2006-10-31 Vortech Engineering, Inc. Supercharger
US7322588B2 (en) * 2004-11-24 2008-01-29 General Motors Corporation Mounting assembly for steering system of vehicles
JP4936511B2 (en) * 2005-03-31 2012-05-23 富士フイルム株式会社 Driving device, photographing device and mobile phone
US20080247692A1 (en) * 2007-04-04 2008-10-09 Pacific Bearing Company Extrudable Polymer Bearing Insert
US8287254B2 (en) * 2007-11-30 2012-10-16 GM Global Technology Operations LLC Motor and pump assembly having improved sealing characteristics
KR100957677B1 (en) * 2008-05-27 2010-05-13 주식회사 유엔아이 Method for producing flame retardant resin composition containing rice husk carbide
US8419487B2 (en) * 2009-08-13 2013-04-16 Jack Parker Internally mounted watercraft rowing fin system
US9719256B2 (en) * 2011-02-25 2017-08-01 Joe's Eats, Llc Apparatus and methods for truss assembly
CN104781566B (en) 2012-09-25 2017-02-15 费德罗-莫格尔公司 ball joint with improved upper bearing and method of construction thereof
JP5686827B2 (en) * 2013-01-23 2015-03-18 株式会社鷺宮製作所 Centrifugal pump
CN103740050B (en) * 2014-01-03 2016-03-09 佛山职业技术学院 The preparation method of a kind of air-conditioner base plate and air-conditioner base plate
BR112018015443B1 (en) * 2016-02-16 2023-10-24 Inventio Ag PULLEY FOR AN ELEVATOR, ELEVATOR AND METHOD FOR MANUFACTURING A PULLEY FOR AN ELEVATOR
US20180297802A1 (en) * 2017-04-13 2018-10-18 Ricoh Company, Ltd. Detector, sheet conveying device incorporating the detector, sheet feeding device incorporating the detector, image forming apparatus incorporating the detector, and image reading device incorporating the detector
CN107871564A (en) * 2017-09-30 2018-04-03 重庆鸽牌电线电缆有限公司 A kind of manufacture method of nylon wire

Citations (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2128087A (en) * 1936-06-10 1938-08-23 Thomas L Gatke Self-lubricating bearing
US3768640A (en) * 1971-07-16 1973-10-30 A Piscatelli Novel cloth winding board
US4115283A (en) * 1975-12-12 1978-09-19 Phillips Petroleum Company Antifriction composition
US4196013A (en) * 1978-10-23 1980-04-01 Cabot Corporation Oxidation resistant asphalt compositions
US4466932A (en) * 1981-12-30 1984-08-21 Kanebo Ltd. Process for producing carbon articles
US4699573A (en) * 1981-10-13 1987-10-13 Westinghouse Electric Corp. Transformer oil pump bearing material
US4877813A (en) * 1984-10-22 1989-10-31 Taiho Kogyo Co., Ltd. Bearing resin material
US4960827A (en) * 1984-12-27 1990-10-02 Asahi Glass Company, Ltd. Curable resin composition
US5026762A (en) * 1989-05-25 1991-06-25 The Yokohama Rubber Co., Ltd. Rubber composition for all-weather tires
US5236784A (en) * 1987-02-09 1993-08-17 Kabushiki Kaisha Sankyo Seiki Seisakusho Bearing material and plastic bearing
US5304422A (en) * 1990-09-19 1994-04-19 Bando Chemical Industries, Ltd. Low friction polyamide, polyethylene, P.T.F.E. resin
US5346737A (en) * 1991-11-21 1994-09-13 E. I. Du Pont De Nemours And Company Lubricated polyacetal compositions
US5357163A (en) * 1992-05-08 1994-10-18 Matsushita Electric Industrial Co., Ltd. Motor with dynamic-pressure type bearing device
US5360633A (en) * 1993-01-14 1994-11-01 Uncle Ben's, Inc. Rice hull ash
US5432213A (en) * 1992-09-19 1995-07-11 Samsung General Chemicals Co., Ltd. Water-permeable resinous composition for road paving of high strength and blocks and pavement thereof
US5432224A (en) * 1988-02-18 1995-07-11 Sanyo Chemical Industries, Ltd. Moldable composition, process for producing sintered body therefrom and products from same
US5549394A (en) * 1994-11-10 1996-08-27 Hycomp, Inc. Bearing arrangement having a polyimide graphite-fiber reinforced composite embedded therein
US5591279A (en) * 1993-05-20 1997-01-07 The Yokohama Rubber Co., Ltd. Pneumatic vehicle tire
US5641275A (en) * 1995-01-26 1997-06-24 Ansimag Inc. Grooved shaft for a magnetic-drive centrifugal pump
US5697709A (en) * 1995-07-18 1997-12-16 Ntn Corporation Dynamic pressure type bearing device
US5730916A (en) * 1994-06-01 1998-03-24 Sgl Technik Gmbh Process for manufacturing essentially carbon filler or distributing body for flowing liquids
US5731373A (en) * 1994-12-26 1998-03-24 Ntn Corporation Slide bearing slide bearing assembly and small motor
US5762699A (en) * 1997-05-05 1998-06-09 K.A.E. Paving Consultants, Inc. Pavement aggregate treating composition
US5916499A (en) * 1996-10-01 1999-06-29 Sanwa Yushi Kabushiki Kaisha Method for producing porous carbon material product
US6196722B1 (en) * 1998-01-13 2001-03-06 Matsushita Electric Industrial Co., Ltd. Hydrodynamic bearing
US6211592B1 (en) * 1999-03-29 2001-04-03 Nidec Corporation Motor for driving storage disks
US6395677B1 (en) * 2000-12-15 2002-05-28 Minebea Co., Ltd. Material for bearing retainer
US6404089B1 (en) * 2000-07-21 2002-06-11 Mark R. Tomion Electrodynamic field generator
US20020111388A1 (en) * 2000-12-15 2002-08-15 Kazuo Hokkirigawa Material for bearing rolling element
US20020114548A1 (en) * 2000-12-15 2002-08-22 Kazuo Hokkirigawa Sleeve bearing arrangement
US20020114549A1 (en) * 2001-02-21 2002-08-22 Kazuo Hokkirigawa Special type bearing device
US6456458B1 (en) * 1998-08-08 2002-09-24 Nidec Corporation Disk-drive motor rotating on a magnetically counterbalanced single hydrodynamic thrust bearing
US20020152694A1 (en) * 2001-04-19 2002-10-24 Kazuo Hokkirigawa Weather-resistant exterior building material
US20020152697A1 (en) * 2001-04-19 2002-10-24 Kazuo Hokkirigawa Roofing tile and snow-melting, tiled roof using the same
US20020152644A1 (en) * 2001-04-19 2002-10-24 Kazuo Hokkirigawa Stud and shoe provided with the studs
US20020158529A1 (en) * 2001-04-24 2002-10-31 Yulan Liu Ferrofluid pivot bearing
US20020174771A1 (en) * 2001-05-25 2002-11-28 Kazuo Hokkirigawa Air cleaning filter
US20020175118A1 (en) * 2001-05-25 2002-11-28 Kazuo Hokkirigawa Water purification filter
US20020174605A1 (en) * 2001-05-25 2002-11-28 Kazuo Hokkirigawa Polishing compound for sheet metal coating
US20020192469A1 (en) * 2001-05-25 2002-12-19 Kazuo Hokkirigawa Deodorizing and absorbing material
US6513979B2 (en) * 2000-08-22 2003-02-04 Ntn Corporation Hydrodynamic oil-impregnated sintered bearing unit
US20030048577A1 (en) * 2001-08-27 2003-03-13 Shun Kayama Spindle motor and information recording and/or reproducing apparatus having this spindle motor
US6550508B1 (en) * 1998-11-27 2003-04-22 The Yokohama Rubber Co., Ltd. Rubber composition for tire tread having high performance on ice and pneumatic tire using the same
US6582130B2 (en) * 2000-11-21 2003-06-24 Nsk Ltd. Rolling bearing and bearing apparatus
US20030134104A1 (en) * 2001-12-25 2003-07-17 Kazuo Hokkirigawa CRB or CRBC fine powder dispersing foam-molded synthetic resin material, method for preparing same and uses thereof
US20030229161A1 (en) * 2002-03-01 2003-12-11 Minebea, Co., Ltd. Low-friction, high-dispersion synthetic resin compositon containing fine particles of RB ceramic or CRB ceramic and a method for its preparation
US6685356B2 (en) * 2001-04-04 2004-02-03 Matsushita Electric Industrial Co., Ltd. Liquid bearing unit and magnetic disk device using the same
US20040132881A1 (en) * 2003-01-07 2004-07-08 Minebea Co., Ltd. Oil repelling agent
US6777360B2 (en) * 2001-02-13 2004-08-17 Minebea Co., Ltd. Ceramic material, method of producing same, and formed product thereof
US20040165797A1 (en) * 2003-02-24 2004-08-26 Nidec Corporation Hydrodynamic bearing, spindle motor using the same and disc drive apparatus provided with spindle motor

Family Cites Families (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US174771A (en) * 1876-03-14 buoadwell
US114549A (en) * 1871-05-09 Improvement in horse-powers
US152644A (en) * 1874-06-30 Improvement in fruit-driers
US152697A (en) * 1874-06-30 Improvement in compounds for cleaning paints
US174605A (en) * 1876-03-07 Improvement in shirts
US152694A (en) * 1874-06-30 Improvement in organ-couplers
US114548A (en) * 1871-05-09 Improvement in window-screens
US111388A (en) * 1871-01-31 Improvement in rolls for hair-dressing
US2002A (en) * 1841-03-12 Tor and planter for plowing
JPS4918458B1 (en) * 1970-05-02 1974-05-10
US3787229A (en) * 1971-02-17 1974-01-22 Union Carbide Corp Low-friction, wear-resistant material
DE2345460A1 (en) 1973-09-08 1975-03-20 Basf Ag POLYESTER MOLDING COMPOUNDS WITH IMPROVED SLIDING PROPERTIES
US4112283A (en) * 1977-03-18 1978-09-05 James Lathrop Distributor cap and dust shield with hermetic sealing and moisture detection apparatus
US4133588A (en) * 1978-01-06 1979-01-09 Industrial Molding Corporation Ball separator for ball bearing
US4354686A (en) * 1979-07-06 1982-10-19 Matsushita Electric Industrial Co., Ltd. Contact-free sealing member
DE3173273D1 (en) * 1980-11-07 1986-01-30 Nat Res Dev Improvements in or relating to fluid bearings
US4704712A (en) * 1985-06-24 1987-11-03 Rca Corporation Low-friction slide apparatus for optical disc translation stage
US4749283A (en) * 1985-09-12 1988-06-07 Canon Kabushiki Kaisha Static pressure bearing
US4702041A (en) * 1986-07-09 1987-10-27 Corning Glass Works Prevention of foreign material intrusion in an air slide for machines
US6193793B1 (en) 1988-01-28 2001-02-27 Howard W. Long Asphaltic compositions and uses therefor
GB8815990D0 (en) * 1988-07-05 1988-08-10 T & N Technology Ltd Bearings
US5104237A (en) * 1990-11-08 1992-04-14 Advanced Engineering Systems Operations & Products, Inc. (Aesop) Self-compensating hydrostatic linear motion bearing
JPH0532797A (en) 1991-07-31 1993-02-09 Japan Steel Works Ltd:The Sliding bearing material, sliding bearing material pellet, and sliding bearing member using the same
DE69328681T2 (en) * 1992-05-15 2000-09-28 Hoechst Celanese Corp., Summit SELF-LUBRICATING COMPOSITION CONTAINING POLYBENZIMIDAZOLE
DE4222140C2 (en) * 1992-07-06 1994-06-16 Heinzl Joachim Miniature aerostatic bearing
JP3128709B2 (en) * 1992-08-04 2001-01-29 株式会社新川 Non-contact moving table
US6472042B1 (en) * 1994-02-10 2002-10-29 Dow Global Technologies Inc. Highly filled thermoplastic compositions
JPH07268126A (en) 1994-03-31 1995-10-17 Ntn Corp Lubricating resin composition
JPH0953640A (en) * 1995-08-18 1997-02-25 Mitsutoyo Corp Static pressure bearing device
US5879791A (en) * 1995-10-02 1999-03-09 Daido Metal Company Ltd. Wet type sliding apparatus comprising thrust bearing
GB2307947B (en) 1995-12-08 1999-08-18 Aisan Ind Magnetically coupled pump
JPH1095647A (en) 1995-12-28 1998-04-14 Toray Ind Inc Ceramic aggregate, its production and pavement structure
JP3370541B2 (en) 1997-02-07 2003-01-27 横浜ゴム株式会社 Rubber composition for studless tires
US6033118A (en) * 1997-03-05 2000-03-07 Nsk Ltd. Hydro-dynamic fluid bearing device and manufacturing method of the same
JP3400924B2 (en) 1997-03-05 2003-04-28 東芝テック株式会社 Electric pump
CA2285079A1 (en) 1997-03-26 1998-10-01 Ricegrowers' Co-Operative Limited Insulation material
US6172847B1 (en) * 1997-03-27 2001-01-09 Nsk Ltd. Rotational assembly for disc drive device having small runout and reduced axial displacement
JPH1121407A (en) 1997-06-27 1999-01-26 Nok Corp Tetrafluoroethylene resin composition
US6448307B1 (en) * 1997-09-02 2002-09-10 Xyleco, Inc. Compositions of texturized fibrous materials
US5971614A (en) * 1997-09-08 1999-10-26 Aesop, Inc. Modular hydrostatic bearing with carriage form-fit to PR
US5989444A (en) * 1998-02-13 1999-11-23 Zywno; Marek Fluid bearings and vacuum chucks and methods for producing same
JP2000121861A (en) 1998-10-09 2000-04-28 Japan Aviation Electronics Industry Ltd Optical fiber guide
JP2000266052A (en) 1999-03-15 2000-09-26 Nsk Ltd Method of treating oil repellent for fluid bearing device and fluid bearing device using the oil repellent
JP2001002742A (en) 1999-06-21 2001-01-09 Hitachi Chem Co Ltd Photosetting resin composition and coating material
FR2796680B1 (en) * 1999-07-23 2001-09-14 Skf France CAGE DEVICE FOR BALL BEARING AND ASSOCIATED BEARING
JP2001089273A (en) 1999-09-17 2001-04-03 Aaru Dakku:Kk Fertilizer, soil conditioner, wafer quality reforming material and deodorant utilizing carbonized rice bran as well as rust preventive method
JP3578948B2 (en) 1999-10-01 2004-10-20 日本電産株式会社 motor
JP2001178978A (en) 1999-12-24 2001-07-03 Juki Corp sewing machine
JP4436532B2 (en) 2000-04-24 2010-03-24 パナソニック株式会社 Hydrodynamic bearing device for magnetic disk drive
JP4701349B2 (en) 2001-03-26 2011-06-15 独立行政法人産業技術総合研究所 Heat treatment of porcelain aggregate
US20040165791A1 (en) 2003-02-21 2004-08-26 Ted Kaltanji Dental image storage and retrieval apparatus

Patent Citations (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2128087A (en) * 1936-06-10 1938-08-23 Thomas L Gatke Self-lubricating bearing
US3768640A (en) * 1971-07-16 1973-10-30 A Piscatelli Novel cloth winding board
US4115283A (en) * 1975-12-12 1978-09-19 Phillips Petroleum Company Antifriction composition
US4196013A (en) * 1978-10-23 1980-04-01 Cabot Corporation Oxidation resistant asphalt compositions
US4699573A (en) * 1981-10-13 1987-10-13 Westinghouse Electric Corp. Transformer oil pump bearing material
US4466932A (en) * 1981-12-30 1984-08-21 Kanebo Ltd. Process for producing carbon articles
US4877813A (en) * 1984-10-22 1989-10-31 Taiho Kogyo Co., Ltd. Bearing resin material
US4960827A (en) * 1984-12-27 1990-10-02 Asahi Glass Company, Ltd. Curable resin composition
US5236784A (en) * 1987-02-09 1993-08-17 Kabushiki Kaisha Sankyo Seiki Seisakusho Bearing material and plastic bearing
US5432224A (en) * 1988-02-18 1995-07-11 Sanyo Chemical Industries, Ltd. Moldable composition, process for producing sintered body therefrom and products from same
US5026762A (en) * 1989-05-25 1991-06-25 The Yokohama Rubber Co., Ltd. Rubber composition for all-weather tires
US5304422A (en) * 1990-09-19 1994-04-19 Bando Chemical Industries, Ltd. Low friction polyamide, polyethylene, P.T.F.E. resin
US5346737A (en) * 1991-11-21 1994-09-13 E. I. Du Pont De Nemours And Company Lubricated polyacetal compositions
US5357163A (en) * 1992-05-08 1994-10-18 Matsushita Electric Industrial Co., Ltd. Motor with dynamic-pressure type bearing device
US5432213A (en) * 1992-09-19 1995-07-11 Samsung General Chemicals Co., Ltd. Water-permeable resinous composition for road paving of high strength and blocks and pavement thereof
US5360633A (en) * 1993-01-14 1994-11-01 Uncle Ben's, Inc. Rice hull ash
US5591279A (en) * 1993-05-20 1997-01-07 The Yokohama Rubber Co., Ltd. Pneumatic vehicle tire
US5730916A (en) * 1994-06-01 1998-03-24 Sgl Technik Gmbh Process for manufacturing essentially carbon filler or distributing body for flowing liquids
US5549394A (en) * 1994-11-10 1996-08-27 Hycomp, Inc. Bearing arrangement having a polyimide graphite-fiber reinforced composite embedded therein
US5731373A (en) * 1994-12-26 1998-03-24 Ntn Corporation Slide bearing slide bearing assembly and small motor
US5641275A (en) * 1995-01-26 1997-06-24 Ansimag Inc. Grooved shaft for a magnetic-drive centrifugal pump
US5697709A (en) * 1995-07-18 1997-12-16 Ntn Corporation Dynamic pressure type bearing device
US5916499A (en) * 1996-10-01 1999-06-29 Sanwa Yushi Kabushiki Kaisha Method for producing porous carbon material product
US5762699A (en) * 1997-05-05 1998-06-09 K.A.E. Paving Consultants, Inc. Pavement aggregate treating composition
US6196722B1 (en) * 1998-01-13 2001-03-06 Matsushita Electric Industrial Co., Ltd. Hydrodynamic bearing
US6456458B1 (en) * 1998-08-08 2002-09-24 Nidec Corporation Disk-drive motor rotating on a magnetically counterbalanced single hydrodynamic thrust bearing
US6550508B1 (en) * 1998-11-27 2003-04-22 The Yokohama Rubber Co., Ltd. Rubber composition for tire tread having high performance on ice and pneumatic tire using the same
US6211592B1 (en) * 1999-03-29 2001-04-03 Nidec Corporation Motor for driving storage disks
US6404089B1 (en) * 2000-07-21 2002-06-11 Mark R. Tomion Electrodynamic field generator
US6513979B2 (en) * 2000-08-22 2003-02-04 Ntn Corporation Hydrodynamic oil-impregnated sintered bearing unit
US6582130B2 (en) * 2000-11-21 2003-06-24 Nsk Ltd. Rolling bearing and bearing apparatus
US6395677B1 (en) * 2000-12-15 2002-05-28 Minebea Co., Ltd. Material for bearing retainer
US20020111388A1 (en) * 2000-12-15 2002-08-15 Kazuo Hokkirigawa Material for bearing rolling element
US6573215B2 (en) * 2000-12-15 2003-06-03 Minebea Co., Ltd. Material for bearing rolling element
US20020114548A1 (en) * 2000-12-15 2002-08-22 Kazuo Hokkirigawa Sleeve bearing arrangement
US6712517B2 (en) * 2000-12-15 2004-03-30 Minebea Co., Ltd. Sleeve bearing arrangement
US6777360B2 (en) * 2001-02-13 2004-08-17 Minebea Co., Ltd. Ceramic material, method of producing same, and formed product thereof
US20020114549A1 (en) * 2001-02-21 2002-08-22 Kazuo Hokkirigawa Special type bearing device
US6685356B2 (en) * 2001-04-04 2004-02-03 Matsushita Electric Industrial Co., Ltd. Liquid bearing unit and magnetic disk device using the same
US20020152644A1 (en) * 2001-04-19 2002-10-24 Kazuo Hokkirigawa Stud and shoe provided with the studs
US20020152697A1 (en) * 2001-04-19 2002-10-24 Kazuo Hokkirigawa Roofing tile and snow-melting, tiled roof using the same
US20020152694A1 (en) * 2001-04-19 2002-10-24 Kazuo Hokkirigawa Weather-resistant exterior building material
US20020158529A1 (en) * 2001-04-24 2002-10-31 Yulan Liu Ferrofluid pivot bearing
US20020192469A1 (en) * 2001-05-25 2002-12-19 Kazuo Hokkirigawa Deodorizing and absorbing material
US6494928B1 (en) * 2001-05-25 2002-12-17 Minebea Co., Ltd. Polishing compound for sheet metal coating
US20020174605A1 (en) * 2001-05-25 2002-11-28 Kazuo Hokkirigawa Polishing compound for sheet metal coating
US20020175118A1 (en) * 2001-05-25 2002-11-28 Kazuo Hokkirigawa Water purification filter
US20020174771A1 (en) * 2001-05-25 2002-11-28 Kazuo Hokkirigawa Air cleaning filter
US20030048577A1 (en) * 2001-08-27 2003-03-13 Shun Kayama Spindle motor and information recording and/or reproducing apparatus having this spindle motor
US20030134104A1 (en) * 2001-12-25 2003-07-17 Kazuo Hokkirigawa CRB or CRBC fine powder dispersing foam-molded synthetic resin material, method for preparing same and uses thereof
US20030229161A1 (en) * 2002-03-01 2003-12-11 Minebea, Co., Ltd. Low-friction, high-dispersion synthetic resin compositon containing fine particles of RB ceramic or CRB ceramic and a method for its preparation
US20040013333A1 (en) * 2002-03-01 2004-01-22 Minebea, Co., Ltd. Synthetic resin composites and bearings formed therefrom and method
US6787075B2 (en) * 2002-03-01 2004-09-07 Minebea Co., Ltd. Method of making synthetic resin composition with lubricative underwater properties containing RBC or CRBC fine powder
US20040132881A1 (en) * 2003-01-07 2004-07-08 Minebea Co., Ltd. Oil repelling agent
US20040165797A1 (en) * 2003-02-24 2004-08-26 Nidec Corporation Hydrodynamic bearing, spindle motor using the same and disc drive apparatus provided with spindle motor

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7140778B2 (en) 2002-03-01 2006-11-28 Minebea Co., Ltd. Synthetic resin composites and bearings formed therefrom and method
US20030229161A1 (en) * 2002-03-01 2003-12-11 Minebea, Co., Ltd. Low-friction, high-dispersion synthetic resin compositon containing fine particles of RB ceramic or CRB ceramic and a method for its preparation
US20030179963A1 (en) * 2002-03-01 2003-09-25 Minebea Co., Ltd. Low friction sleeve bearing
US7144932B2 (en) * 2002-03-01 2006-12-05 Minebea Co., Ltd. Low-friction, high-dispersion synthetic resin composition containing fine particles of RB ceramic or CRB ceramic and a method for its preparation
US20030210995A1 (en) * 2002-03-13 2003-11-13 Minebea Co., Ltd. Electrically motorized pump for use in water
US20040031642A1 (en) * 2002-06-05 2004-02-19 Kazuo Hokkirigawa Air purifying sound insulating wall and its applications
US6887288B2 (en) 2002-06-05 2005-05-03 Minebea Co., Ltd. Superfinishing grindstone
US20040132881A1 (en) * 2003-01-07 2004-07-08 Minebea Co., Ltd. Oil repelling agent
US7160622B2 (en) 2003-01-07 2007-01-09 Minebea Co., Ltd. Oil repelling agent
US20040258334A1 (en) * 2003-02-28 2004-12-23 Minebea Co., Ltd. Underwater sleeve bearing and application thereof
US7008196B2 (en) 2003-03-11 2006-03-07 Minebea Co. Ltd. Electrically motorized pump having a submersible sleeve bearing
US9120913B2 (en) 2013-09-30 2015-09-01 Hitachi Metals, Ltd. Elastic composite material and mold product using the same
CN105238043A (en) * 2015-11-09 2016-01-13 安徽省宁国顺昌机械有限公司 Isolating block for slewing bearing

Also Published As

Publication number Publication date
US6787075B2 (en) 2004-09-07
US20030229161A1 (en) 2003-12-11
US7140778B2 (en) 2006-11-28
CN1237118C (en) 2006-01-18
US20030183973A1 (en) 2003-10-02
EP1344791A1 (en) 2003-09-17
US20040013333A1 (en) 2004-01-22
CN1453310A (en) 2003-11-05
US7144932B2 (en) 2006-12-05
EP1347009A1 (en) 2003-09-24
CN1451690A (en) 2003-10-29
US20050032939A1 (en) 2005-02-10
US20030179963A1 (en) 2003-09-25
CN1477152A (en) 2004-02-25

Similar Documents

Publication Publication Date Title
US20030220421A1 (en) Low noise synthetic resin composition and method
JP6165132B2 (en) Novel self-lubricating surface coating composition
Wang et al. The friction and wear properties of nanometer ZrO2‐filled polyetheretherketone
US3898361A (en) Fluoroelastomer-based composite material
EP0120200B1 (en) Fluoroelastomer-based friction material having improved frictional properties
US7452926B2 (en) Resin pulley formed of a resin composition having a phenol resin, an inorganic powder , a reinforcing fiber, and a lubricant
Eshkobilov et al. Investigation of the process of electrification of composite polymer coatings in the case of frictional interaction with the fibrous mass
US5158695A (en) Diamond-based antifriction material
EP1440955B1 (en) A seal assembly containing a sliding element and the use of a sliding element for seals
US4045402A (en) Fluoroelastomer-polyacrylate based friction material
US4051100A (en) Fluoroelastomer-based composite material
US3926818A (en) Composite bearing materials
JPH03292366A (en) Wear-resistant resin composition
KR101059461B1 (en) Lubricants and sliding members
CN109517381A (en) A kind of high-strength abrasion-proof engineering plastics and preparation method thereof
EP1528081A2 (en) Synthetic resin composites and bearings formed therefrom and method
CA1044395A (en) Fluoroelastomer-polyacrylate based friction material
EP1518891A1 (en) Synthetic resin and bearing parts made thereform
JP2004108499A (en) Synthetic resin compound for sliding bearings and sliding bearing molding the same
KR101337430B1 (en) Organic type friction material for wind generator yaw brake
Talib et al. Effect of phenolic resin on the friction behaviors with respect to temperature and operating speed
Sathishkumar Tribological behaviors of glass fiber with fillers reinforced hybrid polymer composites
KR20050120864A (en) Addition composition of polymeric matrix material for improvement of friction and wear properties
Birsan et al. Tribological Behavior of Clay/Epoxy Composites
JPH11280765A (en) Sliding member

Legal Events

Date Code Title Description
AS Assignment

Owner name: MINEBEA CO., LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HOKKIRIGAWA, KAZUO;AKIYAMA, MOTOHARU;KAWAMURA, MORINOBU;REEL/FRAME:014231/0669;SIGNING DATES FROM 20030312 TO 20030318

Owner name: MINEBEA CO., LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HOKKIRIGAWA, KAZUO;AKIYAMA, MOTOHARU;KAWAMURA, MORINOBU;REEL/FRAME:014231/0737;SIGNING DATES FROM 20030618 TO 20030619

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION