US3541872A - Cushion and cover compositions for v-belts - Google Patents
Cushion and cover compositions for v-belts Download PDFInfo
- Publication number
- US3541872A US3541872A US703248A US3541872DA US3541872A US 3541872 A US3541872 A US 3541872A US 703248 A US703248 A US 703248A US 3541872D A US3541872D A US 3541872DA US 3541872 A US3541872 A US 3541872A
- Authority
- US
- United States
- Prior art keywords
- belts
- cushion
- parts
- belt
- fabric
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title description 28
- 239000004744 fabric Substances 0.000 description 30
- 150000001875 compounds Chemical class 0.000 description 16
- 229920001084 poly(chloroprene) Polymers 0.000 description 14
- 229920005989 resin Polymers 0.000 description 13
- 239000011347 resin Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 11
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 10
- -1 ethylene, propylene Chemical group 0.000 description 10
- 229920000742 Cotton Polymers 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 8
- 239000004810 polytetrafluoroethylene Substances 0.000 description 8
- 239000000835 fiber Substances 0.000 description 7
- 238000005299 abrasion Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 239000006229 carbon black Substances 0.000 description 5
- 150000001993 dienes Chemical class 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229920001778 nylon Polymers 0.000 description 5
- 239000011787 zinc oxide Substances 0.000 description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 4
- 230000032798 delamination Effects 0.000 description 4
- 238000009413 insulation Methods 0.000 description 4
- 239000002964 rayon Substances 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- LLVWLCAZSOLOTF-UHFFFAOYSA-N 1-methyl-4-[1,4,4-tris(4-methylphenyl)buta-1,3-dienyl]benzene Chemical compound C1=CC(C)=CC=C1C(C=1C=CC(C)=CC=1)=CC=C(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 LLVWLCAZSOLOTF-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000004627 regenerated cellulose Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- 229920001368 Crepe rubber Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004812 Fluorinated ethylene propylene Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- SPAGIJMPHSUYSE-UHFFFAOYSA-N Magnesium peroxide Chemical compound [Mg+2].[O-][O-] SPAGIJMPHSUYSE-UHFFFAOYSA-N 0.000 description 1
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000013305 flexible fiber Substances 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920009441 perflouroethylene propylene Polymers 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010059 sulfur vulcanization Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D29/00—Producing belts or bands
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L11/00—Compositions of homopolymers or copolymers of chloroprene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/02—Cellulose; Modified cellulose
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
- C08L23/28—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or halogen-containing compounds
- C08L23/283—Iso-olefin halogenated homopolymers or copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
Definitions
- This invention relates to cushion stocks for V-belts, elastomeric impregnated fabric envelopes for V-belts, V- belts containing said cushion stocks and fabric envelopes, and a process for improving the resistance to failure due to flexing of said V-belts.
- V-belts characterized by a cross section in the form of a trapezoid or truncated V which wedgingly engages the similarly shaped peripheral groove of a V-pulley are employed in an ever increasing number of applications.
- a primary reason for this popularity is the improved load carrying and power transmitting capability afforded by the forced contact between the sides of the belt and the sides of the pulley groove Whhich resist slippage of the belt in the pulley.
- These well known belts are normally characterized by such basic elements as a tension member composed of a rubber insulated cord layer, and a compression (cushion) section.
- An example of a belt of this type is described and illustrated (FIG. 3) in US. Pat. 3,051,212.
- the belt is covered by a rubberized fabric envelope which covers the'entire surface of the belt.
- a rubberized fabric envelope which covers the'entire surface of the belt.
- An example of such an envelope is discussed and shown in US. Pat. 3,260,126.
- no envelope is used, resulting in what is commonly known as a molded or raw edge belt.
- the resistance of the belts to failure due to flexing has become increasingly important.
- the cushion section of the belt is not covered by a rubberized fabric the surface of the cushion after vulcanization can possess imperfections which not only detract from the appearance of the cushion section, but in addition, provide sites for flex cracking and other forms of deterioration to occur.
- V-belts It is therefore desirable to improve the performance and appearance of V-belts. It is desirable that the resistance to failure due to flexing be improved. Such failure can take the form of a delamination of the elements of the belt and cord separation. Increased abrasion resistance is also desirable. It is also desirable to provide cushion sections with less surface imperfections in order to improve the appearance of the surface of the cushion stock and also to aid in preventing flex cracking and other forms of deterioration.
- Some of the objects of the present invention are accomplished by blending a carbon black loaded composition comprising (A) 100 parts by weight of at least one p CC elastomeric compound comprising (1) from about 50 to 100 parts by weight per 100 parts by weight of the elastomeric compound of polychloroprene and (2) from 0 to about 50 parts by weight per 100 parts by weight of the elastomeric compound of at least one rubbery diene polymer, (B) from about 0 to about parts by weight per parts by weight of the elastomeric compound of at least one flexible filamentary material and (C) from about 0.5 to about 20.0 parts by weight per 100 parts by weight of the elastomeric compound of at least one polyfluorohydrocarbon resin and then building a V-belt using the above composition to form the cushion portion of the belt and vulcanizing said V-belt.
- Some objects are accomplished by impregnating fabric with the above composition to form fabric envelopes for V-belts. Other objects will appear subsequently herein.
- the elastomeric compound consists essentially of polychloroprene, i.e., the rubbery polymer of 2- chlorobutadiene-l,3.
- This material is designated as ASTM D 14l856T at (C).
- Rubbery diene polymers which may be used in combination with the polychloroprene include natural rubber, such as crepe rubber, and synthetic rubbers such as homopolymers of a conjugated 1,3-diene such as isoprene and butadiene, and in particular, polyisoprenes and polybutadienes having essentially all of their repeating units combined in a cis-l,4 structure; copolymers of a conjugated 1,3-diene such as isoprene and butadiene with up to 50 percent by weight of at least one copolymerizable monomer such as styrene and acr lonitrile; and polymers of monoolefins containing unsaturation, i.e., carbon to carbon double bonds, such as terpolymers of ethylene, propylene and a nonconjugated diene.
- natural rubber such as crepe rubber
- synthetic rubbers such as homopolymers of a conjugated 1,3-diene such as iso
- the flexible filamentary material to be used in the prac' tice of the present invention may be any flexible fiber of a shortened length which is generally used to increase the stiffness and hardness of cushion stocks.
- Such usage of fibers is noted in US. Pat. 3,051,212, column 4, lines 67 and 68.
- Well known fibers such as cotton linters and chopped or ground polyamides, such as nylons; regenerated cellulose such as rayon; and polyester fibers are exemplary of the types of the materials that may be used as flexible filamentary materials.
- the materials should be of such size that they can be dispersed uniformly throughout the cushion stock, and of such size to provide an increase in stiffness and hardness of the cushion stocks. Preferably from about 5 to about 30 parts b weight of the flexible filamentary material are used.
- Polyfluorohydrocarbon resins which have polymer lubricating properties, which may be used in the practice of the present invention are essentially completely fluoronated polymers such as polytetrafluoroethylene and essentially completely fluorinated ethylene propylene copolymers such as those made by copolymerizing hexafluoropropylene and tetrafluoroethylene.
- the method of combining the components of the cushion stock is not normally critical.
- the elastomeric compound, flexible filamentary material and polyfluorohydrocarbon resin may be mixed by such methods as Banbury mixing and open mill mixing.
- the components may be mixed in any order, in increments, and in any combination.
- any conventional vulcanization system may be used to vulcanize the cushion stock.
- the elastomeric compound of the cushion stock consists essentially of polychloropene
- materials such as zinc oxide may be used to vulcanize the cushion stock.
- diene polymers are used as a portion of the elastomeric compound it is preferred that some sulfur vulcanization system be used.
- Any conventional carbon black may be used to load the cushion stock.
- the level of black should normally be from about 10 to about 90 parts by weight per 100 parts by weight of the elastomeric compound. A range of from about 20 to about 40 parts by weight is preferred.
- the cushion stock composition may also be used to impregnate fabric to form fabric envelopes for V-belts, with the qualification that it preferably contains essentially no fiber loading.
- An example of a fabric envelope for a V-belt is shown in FIG. 6 and discussed at column 5, lines 26 to 28 of US. Pat. 3,260,126.
- the fabric may be any conventional V-belt fabric, e.g., cotton, rayon, nylon and polyesters.
- the fabric may be impregnated in any conventional manner, for example by swelling the elastomer in an organic solvent to form a dough-like composition, spreading the dough-like composition on the fabric and driving off the organic solvent. Said envelopes improve the resistance to failure due to flexing of V-belts.
- EXAMPLE 1 Eight V-belts, A through H, having tensile and cushion elements were fabricated using identical trapezoid type construction and vulcanized. The cushion portions of the belts were devoid of any fabric envelopes. The compounds and cords used in constructing the V-belts were the same with the exception of the cushion portion of the belts. The cushion portion of belts A through D was prepared by milling together the following formulation.
- the cushion portion of belts E through H was prepared by milling together the following formulation.
- the nonproductive polychloroprene stock contained 100 parts by weight of polychloroprene as its sole elas tomeric component, 20.0 parts of PEP carbon black, magnesium dioxide, processing oil, stearic acid, phenylbetanaphthylamine and phenylalphanaphthylamine.
- the scrap was unvulcanized productive V-belt scrap which had been ground into fine particles.
- the scrap V- belts were similar to belts A through. H regarding both construction and composition.
- the cushion portion did not contain polytetrafiuoroethylene.
- the insulation portion of the V-belt scrap comprised approximately 20 percent by weight of the V-belt scrap.
- the polyester cord comprised about 5 percent by weight.
- the cushion portion comprised about 75 percent by weight.
- the insulation portion contained 100 parts by weight of polychloroprene as its sole elastomeric component, 20.0 parts of PEP black, 10.0 parts of cotton linters, reinforcing silica, magnesium oxide, processing oil, stearic acid, zinc oxide, a polyethylene wax releasing agent and phenylalphanaphthylamine.
- the cushion portion of the V- belt scrap had approximately the same composition as the cushion stocks of belts A to H.
- the cushion stocks in belts A to H were essentially the same, containing approximately 15 percent by weight of chopped fiber,
- both sets of belts contained a tensile portion comprised of polyester cords insulated by an elastomeric formulation similar to the insulation composition described earlier herein.
- EXAM PLE' 2 Cushion stocks for V-belts within the scope of the present invention are also prepared by mixing the fol lowing compounds on an open mill.
- Chopped or ground rayon, nylon and polyester fibers are interchangeable with cotton linters.
- Other essentially completely fiuoronated polyfluorohydrocarbon resins such as essentially completely fluoronated ethylene propoylene copolymers are also interchangeable With polytetrafiuoroethylene.
- Example 3 The belts of Example 1 were dynamically tested on a pulley arrangement according to SAE procedure I637 (SAE Handbook, 1967 edition) at 13 horsepower with the exception that the small pulley was 2.5 inches in di ameter. The time to first failure as indicated by the first parting of any of the elements of the belt from the rest of the belt was recorded.
- the surfaces of the cushion portions of belts A to D also contained some surface imperfections, whereas the surfaces of the cushion portions of belts E to H contained no appreciable surface imperfections.
- Example 3 The belts tested in Example 3 did not possess a fabric envelope surrounding the cushion element. Tests, however, have been run with belts containing a cushion element surrounded by a fabric envelope. The cushion element contained polytetrafiuoroethylene. These belts also showed improved resistance to failure due to flexing. The use of polyfluorohydrocarbon resins also enhances the abrasion resistance of the cushion stocks.
- each belt contained a fabric envelope (cotton/nylon blend) impregnated with a black loaded (50 parts by weight of black) productive polychloroprene stock.
- the fabric was impregnated by swelling the polychloroprene composition with an organic solvent to form a dough-like composition, spreading the dough-like composition on the fabric and driving off the solvent.
- the cushion stock of these eight belts did not contain fiber loading.
- belts contained polytetrafluoroethylene in the polychloroprene portion of the fabric envelope, also known as a fabric cover.
- the other four belts contained no polytetrafluoroethylene in the fabric envelope.
- the belts were tested in a manner similar to that described in Example 3 using a 2,5 idler pulley, a tension of 140 pounds and 14 horsepower.
- belts M through P of the present invention were superior in performance.
- polyfluorohydrocarbon resins also enhances the abrasion resistance of the fabric envelopes.
- a transmission belt having a tension element therein and including at least one flexing portion containing a carbon composition
- the loaded composition of at least one of said portions is comprised of (A) 100 parts of at least one elastomeric compound having (1) from about 50 to 100 parts of polychloroprene and (2) from about to about 50 parts of a different rubbery diene polymer, (B) from about 0 to about 75 parts of at least one flexible filamentary ma- 6 terial, (C) from about 0.5 to about 20.0 parts of at least one polyfluorohydrocarbon resin, and (D) from about 10 to about parts of carbon black, said parts being by weight per parts of elastomeric compound.
- flexing portions is a fabric cover element which at least substantially forms the outer periphery of the belt and is impregnated with said composition and said composition has about 0 part of the flexible filamentary material.
- the flexible filamentary material is selected from the group consisting of a polyamide, regenerated cellulose, polyester and cotton.
- polyfluorohydrocarbon resin is at least one resin selected from the group consisting of polytetrafluoroethylene and essentially completely fluoronated ethylene Propylene copolymer resins.
- a process for improving the flex life of a transmission belt having a tension element therein and including at least one flexing portion containing an elastomeric composition comprising the step of forming at least one of the flexing portions from the elastomeric composition of claim 1.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Reinforced Plastic Materials (AREA)
- Woven Fabrics (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US70324868A | 1968-02-06 | 1968-02-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3541872A true US3541872A (en) | 1970-11-24 |
Family
ID=24824632
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US703248A Expired - Lifetime US3541872A (en) | 1968-02-06 | 1968-02-06 | Cushion and cover compositions for v-belts |
Country Status (7)
Country | Link |
---|---|
US (1) | US3541872A (en)van) |
BE (1) | BE727859A (en)van) |
BR (1) | BR6905987D0 (en)van) |
DE (1) | DE1902654A1 (en)van) |
FR (1) | FR2001385A1 (en)van) |
GB (1) | GB1214284A (en)van) |
NL (1) | NL6901898A (en)van) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4634726A (en) * | 1983-12-12 | 1987-01-06 | The Goodyear Tire & Rubber Company | Cushion stock for power transmission belts |
US5064904A (en) * | 1989-03-29 | 1991-11-12 | Bayer Ag | Suitable polychloroprene materials for the production of high-damping vulcanisates |
US20030216206A1 (en) * | 2002-03-25 | 2003-11-20 | Toyoda Koki Kabushiki Kaisha | Pulley |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2273711A (en) * | 1992-12-23 | 1994-06-29 | Tba Belting Ltd | Drive belts |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2631463A (en) * | 1946-11-12 | 1953-03-17 | Dayton Rubber Company | Cord belt |
US3002938A (en) * | 1958-08-25 | 1961-10-03 | Davol Rubber Co | Method of making natural rubber resistant to ozone by the addition of polytetrafluorethylene and product thereof |
US3011221A (en) * | 1957-05-15 | 1961-12-05 | Dayco Corp | Textile fiber drafting apron |
US3223676A (en) * | 1960-07-07 | 1965-12-14 | Johns Manville | Process for producing a molded gasket from polytetrafluoroethylene and a butadiene-acrylonitrile elastomer |
-
1968
- 1968-02-06 US US703248A patent/US3541872A/en not_active Expired - Lifetime
-
1969
- 1969-01-13 GB GB0892/69A patent/GB1214284A/en not_active Expired
- 1969-01-15 DE DE19691902654 patent/DE1902654A1/de active Pending
- 1969-01-30 FR FR6901884A patent/FR2001385A1/fr not_active Withdrawn
- 1969-01-30 BR BR205987/69A patent/BR6905987D0/pt unknown
- 1969-02-03 BE BE727859D patent/BE727859A/xx unknown
- 1969-02-06 NL NL6901898A patent/NL6901898A/xx unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2631463A (en) * | 1946-11-12 | 1953-03-17 | Dayton Rubber Company | Cord belt |
US3011221A (en) * | 1957-05-15 | 1961-12-05 | Dayco Corp | Textile fiber drafting apron |
US3002938A (en) * | 1958-08-25 | 1961-10-03 | Davol Rubber Co | Method of making natural rubber resistant to ozone by the addition of polytetrafluorethylene and product thereof |
US3223676A (en) * | 1960-07-07 | 1965-12-14 | Johns Manville | Process for producing a molded gasket from polytetrafluoroethylene and a butadiene-acrylonitrile elastomer |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4634726A (en) * | 1983-12-12 | 1987-01-06 | The Goodyear Tire & Rubber Company | Cushion stock for power transmission belts |
US5064904A (en) * | 1989-03-29 | 1991-11-12 | Bayer Ag | Suitable polychloroprene materials for the production of high-damping vulcanisates |
US20030216206A1 (en) * | 2002-03-25 | 2003-11-20 | Toyoda Koki Kabushiki Kaisha | Pulley |
US6929575B2 (en) * | 2002-03-25 | 2005-08-16 | Toyoda Koki Kabushiki Kaisha | Pulley |
Also Published As
Publication number | Publication date |
---|---|
GB1214284A (en) | 1970-12-02 |
NL6901898A (en)van) | 1969-08-08 |
FR2001385A1 (en)van) | 1969-09-26 |
BR6905987D0 (pt) | 1973-01-09 |
DE1902654A1 (de) | 1970-08-20 |
BE727859A (en)van) | 1969-07-16 |
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