CVT belt
09933041 ยท 2018-04-03
Assignee
Inventors
- Bobbie E. South (New Bloomfield, MO, US)
- Jerzy Otremba (Troy, MI, US)
- John Francisco Dayberry (Siloam Springs, AR, US)
Cpc classification
F16G1/28
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16G1/08
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16G5/20
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16G5/06
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
International classification
F16G5/06
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16G5/16
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16G1/08
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
F16G1/28
MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
Abstract
An endless rubber power transmission belt such as a CVT belt having a main belt body with a compression portion, tension portion, an adhesion portion, and a tensile cord in contact with the adhesion portion and embedded between the compression portion and the tension portion, angled sides, and a width to thickness ratio on the order of 2 to 3. At least one of the compression portion, the tension portion and the adhesion portion has an elastomer composition that includes a saturated ethylene-alpha-olefin elastomer, a staple fiber, and a pulp fiber, or an elastomer, a high-modulus staple fiber, and a high-modulus pulp fiber. The pulp fiber constitutes less than 40% of the total high-modulus fiber amount.
Claims
1. An endless rubber CVT belt comprising a main belt body comprising a compression portion, tension portion, an adhesion portion, and a tensile cord in contact with the adhesion portion and embedded between the compression portion and the tension portion, angled sides, and a width to thickness ratio on the order of 2; wherein at least one of the compression portion, the tension portion and the adhesion portion comprises an elastomer composition comprising a saturated ethylene-alpha-olefin elastomer, a staple fiber, and a pulp fiber.
2. The belt of claim 1 wherein the aramid staple fiber is para-aramid and the aramid pulp fiber is para-aramid.
3. The belt of claim 1 wherein the alpha-olefin of the ethylene-alpha-olefin elastomer is octene or butene.
4. The belt of claim 3 wherein the ethylene-alpha-olefin elastomer is ethylene-octene elastomer with an ethylene content in the range of below 75% by weight and a melt flow rate less than 5 gm/10 min. based on ASTM D1238-13 with 2.16 kg at 190? C.
5. The belt of claim 3 wherein the ethylene-alpha-olefin elastomer is ethylene-butene elastomer with an ethylene content in the range of 60.0% to 65.0% by weight.
6. The belt of claim 1 wherein the total amount of the aramid staple fiber and aramid pulp fiber is between 3 and 19 volume percent of the composition and between 1 and 65 phr.
7. The belt of claim 1 wherein the belt exhibits a stiffness on the Dynamic Axial Stiffness Test of greater than 5.0 kN/mm.
8. The belt of claim 1 wherein the belt exhibits a stiffness on the Gates Compression Test of greater than or equal to 5.0 kN/mm at 90? C. and greater than 6.0 kN/mm at room temperature.
9. The belt of claim 1 wherein the overall belt thickness is less than 15 mm.
10. The belt of claim 9 wherein the cord position is closer to the backside than to the underside of the belt.
11. An endless power transmission belt comprising a main belt body comprising: a tensile cord embedded in said belt body, and an elastomer composition comprising an elastomer, a high-modulus staple fiber, and a high-modulus pulp fiber; wherein the high-modulus pulp fiber constitutes less than 40% of the total amount of the high-modulus staple fiber and the high-modulus pulp fiber.
12. The power transmission belt of claim 11 in the form of a toothed belt, a V-belt, or a multi-V-ribbed belt.
13. The belt of claim 11 wherein the elastomer is an ethylene-alpha-olefin elastomer, and the total amount of the high-modulus staple fiber and the high-modulus pulp fiber is between 3 and 19 volume percent of the elastomer composition.
14. The belt of claim 11 wherein the elastomer is a saturated ethylene-alpha-olefin elastomer.
15. The belt of claim 11 wherein the elastomer composition further comprises other elastomers at less than 50% of the total elastomer present by weight.
16. The belt of claim 11 wherein both the high-modulus staple fiber and high-modulus pulp fiber are aramid fibers.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The accompanying drawings, which are incorporated in and form part of the specification in which like numerals designate like parts, illustrate embodiments of the present invention and together with the description, serve to explain the principles of the invention. In the drawings:
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DETAILED DESCRIPTION
(12) The problem of improving CVT belt performance can be tied to the underlying problem of increasing transverse stiffness while improving or at least maintaining a lot of other properties, such as longitudinal flexibility, crack resistance, thermal resistance, frictional properties, hysteretic properties, adhesion, tensile strength, etc.
(13) It has been known that loading of the rubber composition with short fiber for the belt body can lead to increased stiffness. Orienting the fiber in the transverse direction can increase transverse stiffness of the belt while maintaining a higher level of flexibility in the longitudinal direction (anisotropic modulus). However, the problem of mixing, dispersing and orienting high modulus fibers into the rubber composition limits the amount of such fiber that can be practically added. Now it has been discovered that a proper blend of two different fiber types, and judicious choice of the base elastomer can have a dramatic effect on a rubber composition modulus and stiffness of the final compound while still giving improved processing and ultimately improving the resulting CVT belt performance. By shifting the ratio of pulp to staple fiber, while adopting the unique properties of the ethylene-alpha-olefin or polyolefin elastomer, one can obtain a significantly improved level of stiffness in the resulting belt which has in turn resulted in exceptional durability and load carrying capabilities.
(14) Thus, the present invention relates to a rubber composition for a CVT belt. The rubber composition is fiber-loaded with both staple and pulp fibers, preferably aramid fibers. The elastomer is preferably ethylene-alpha-olefin elastomer. The composition is calendered or extruded to orient the fibers (longitudinally in a calendered sheet material), then arranged to be oriented transverse to the belt running direction in the final belt, i.e., axially with respect to the axis of the pulleys or sheaves on which the belt runs. The resulting belt axial or transverse stiffness is in a predetermined range, resulting in significant performance benefits over conventional CVT belts.
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(17) The CVT belt may have cogs on the inside, backside or both sides as illustrated in
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(19) Turning to a more detailed description of the rubber compositions in the CVT belt, the usual definition of rubber or elastomer is used herein, namely a material that can be stretched repeatedly to at least about twice its original length and which will return upon immediate release of the stress to approximately its original length. Herein, the term elastomer or base elastomer will be restricted to the elastomeric polymers used to form the composition, while rubber or rubber composition will be used to indicate a composition including the base elastomer and other compounding ingredients, unless otherwise indicated by the context. Most rubber is given its final properties by compounding the base elastomer with fillers, process aids, anti-degradants, curatives, etc., followed by crosslinking or vulcanizing by heating. The final properties of the fiber-loaded rubber compositions of the present invention may not necessarily achieve more than twice their original length without breaking, particularly in the direction of fiber orientation, so this part of the standard definition may be relaxed herein.
(20) The compounding principles elucidated herein are believed to be applicable to a wide variety of elastomers useful in belts, such as polychloroprene (CR), nitrile-butadiene (NBR, HNBR), polyolefin elastomers including copolymers and terpolymers with unstaturation or those that are fully saturated, natural rubber (NR), and so on. However, the preferred materials are saturated polyolefin elastomers (POE), such as ethylene-alpha-olefin copolymer elastomers, including ethylene-propylene, ethylene-butene, ethylene-pentene, ethylene-octene and so on. By saturated is meant no double bonds in the main chain or pendant thereto, except possibly in one or both end groups. The most preferred elastomers are ethylene-octene elastomer (EOM), ethylene-butene (EBM), and ethylene-propylene elastomers (EPM). In various embodiments, the rubber composition to be described may be used in at least one of the above mentioned belt layers, i.e., adhesion gum layer, overcord layer, and undercord layer, or in two or in all layers. The compositions may include only the base elastomer as the sole elastomer present, or there may be a blend of the base elastomer with one or more other elastomers. The base elastomer is always more than 50% of the total of all elastomers present, preferably more than 70% or 80% or more or about 90% or more, by weight or by volume.
(21) Useful ethylene-octene elastomers may be exemplified by the ENGAGE polyolefin elastomers sold under that trademark by The Dow Chemical Company. The EOM may have a melt index less than or equal to 5, preferably less than equal to 1, or most preferably less than or equal to 0.5 grams/10 minutes (2.16 kg@190? C.) per ASTM D1238-13. The EOM may have a density (g/cc) between 0.850 and 0.875, preferably equal to or between 0.855 and 0.870 density, most preferably between 0.860 and 0.870. The ethylene content may be from 60 to 65 weight percent for EOM.
(22) Useful ethylene-butene elastomers may be exemplified by the ENGAGE polyolefin elastomers sold under that trademark by The Dow Chemical Company and the EXACT copolymers sold under that trademark by ExxonMobil Chemical and the TAFMER copolymers sold under that trademark by Mitsui Chemicals Group. The EBM may have a melt index less than or equal to 5, preferably less than equal to 1, or most preferably less than or equal to 0.5 grams/10 minutes (2.16 kg @ 190? C.) per ASTM D1238-13. The EBM may have a density of equal to or between 0.850 and 0.890, or from 0.850 to 0.880, or from 0.850 to 0.870. The ethylene content may be from 40 to 60 weight percent for EBM.
(23) The belt compositions of various embodiments include both staple or chopped high-modulus fibers, and pulp or fibrillated high-modulus fibers, preferably both of aramid or aromatic polyamide materials.
(24) The preferred aramid fibers that may beneficially be used as a reinforcement of the belt elastomer include meta-aramids, para-aramids, and para-aramid copolymers, such as those sold under the trademarks KEVLAR and NOMEX by DuPont and TECHNORA, CONEX, and TWARON by Teijin. The fibers include both fibrillated or pulped fibers and chopped or staple fiber. For purposes of the present disclosure, the terms fibrillated and pulp shall be used interchangeably to indicate this type of fiber, and the terms, chopped or staple will be used interchangeably to indicate that type of fiber. The fibers may optionally be treated as desired based in part on the fiber and elastomer type to improve their adhesion to the elastomer. An example of a fiber treatment is any suitable resorcinol formaldehyde latex (RFL).
(25) The fibers of the staple or chopped variety may be formed of a suitable aramid or other high-performance fiber and have an aspect ratio or L/D (ratio of fiber length to diameter) preferably equal to 10 or greater. Staple fibers generally have a uniform cross section over their entire length. The staple fibers may have a length from about 0.1 to about 10 mm, or to about 5 mm, preferably from about 1 to about 3 mm. The staple fibers may have a diameter from about 1 to about 30 microns, preferably from about 6 to about 20, or about 10 to 15 microns. A mixture of staple fiber types, lengths, or diameters may be used. Although para-aramid fibers are preferred, the staple fibers may be of other high-performance or high-modulus polymer materials, such as meta-aramid, polybenzobisoxazole (PBO), polyetheretherketone, vinylon, nylon, polyacrylonitrile, liquid crystal polymer, or the like.
(26) The high-modulus fibers of the pulped or fibrillated variety may be processed where possible for a given fiber type to increase their surface area, formed preferably of a suitable para-aramid, and may possess a specific surface area of from about 1 m.sup.2/g to about 15 m.sup.2/g, more preferably of about 3 m.sup.2/g to about 12 m.sup.2/g, most preferably from about 7 m.sup.2/g to about 11 m.sup.2/g; or an average fiber length of from about 0.1 mm to about 5.0 mm, more preferably of from about 0.3 mm to about 3.5 mm, and most preferably of from about 0.5 mm to about 2.0 mm. The pulp fiber may have fibrils of irregular cross section and shape, but primarily, pulp is characterized by the presence of many, much smaller diameter fibrils having been split off of or branched from the original fibers. It may be noted that herein, the term pulp has nothing to do with wood, paper, fruit, fiction or any other common usages from other fields, but is only used here and in the claims as defined herein.
(27) The total amount of pulp and staple fiber in the composition may range from about 1 phr to 65 phr, preferably from about 6 to about 50 phr, or from about 17 to about 35 phr. The amount of aramid pulp or fibrillated fiber used in various embodiments of the invention may beneficially be from about 0.5 to about 25 parts per hundred weight of elastomer (phr); is preferably from about 0.9 to about 20 phr, more preferably from about 1.0 to about 15 phr, and is most preferably from about 2.0 to about 10 phr. The amount of aramid staple fiber used in a preferred embodiment of the invention may beneficially be from about 0.5 to about 40 parts per hundred weight of elastomer (phr); is preferably from about 5 to about 35 phr, more preferably from about 10 to about 30 phr, and is most preferably from about 15 to about 25 phr. The optimum amounts may depend on the amounts and types of each fiber used, the type of elastomer, and the end result desired. The range of aramid pulp content is greater than 0, or greater than 5% or 10%, and less than 100% or 70% or 60% of the total fiber weight. Preferably the aramid pulp weight is less than 50% or 45% or 40% or 35% of the total fiber weight. With saturated polyolefin elastomers such as EOM or EBM elastomers, the higher pulp levels are possible, while for other elastomers such as EPDM or CR, the lower range, less than or equal to 40% or 35% or less of the total fiber, is required.
(28) More directly related to the end properties is the fiber volume percent and the relative amount of pulp as a percent of the total fiber volume. These amounts of pulp and staple fiber are important for, and may be selected for, the desired end properties of the composition as well as for the processability thereof, and may depend on other factors as fiber length and degree of fibrillation and the choice of elastomer. In various embodiments, for example, those based on 1 to 3 mm length para-aramid fiber for both staple and pulp portions in polyolefin elastomers, the total fiber volume percent is advantageously between 3 and 19 volume percent. The total fiber concentration may advantageously be between 5 and 17 volume percent, or between 7 and 15 volume percent. The total volume percent of fiber may be from 9 to 13 volume percent. The range of aramid pulp volume content is greater than 0, or greater than 5% or 10%, and less than 100% or 70% or 60% of the total fiber volume. Preferably the aramid pulp volume content is less than 50% of the total fiber volume. More preferably the pulp level is 40% or less of the total fiber. Most preferably the pulp content is less than 35% of the total fiber content.
(29) The other ingredients in the composition may be selected as usual in the art. One skilled in the relevant art would recognize that the elastomer would preferably be modified to include additional materials, e.g. plasticizers, anti-degradants, reinforcing particulate fillers such as carbon black and silica, curatives, coagents, and possibly other fibers both natural and synthetic such as, cotton, kenaf, hemp, wool, flax, wood fiber, nylon, polyester, rayon, polyvinyl alcohol, polyvinyl acetate, acrylic, etc. If other high-modulus staple fibers, of similar length and reinforcing effect as the primary fibers described above, are included, they should be included in the total fiber content.
(30) For best wear resistance, the polyolefin elastomer compositions may be peroxide cured with suitable coagents. The preferred coagents are metal salts of an ?-?-unsaturated organic acid as disclosed in U.S. Pat. No. 5,610,217, the entire contents of which are hereby incorporated herein by reference. Exemplary metal salts are zinc diacrylate and zinc dimethacrylate (ZDMA).
(31) Mixing, Calendering, Molding, Etc.
(32) The fibers may be added to the elastomer composition via any suitable or conventional technique, such as by first incorporating fibrillated fibers in a suitable first elastomer composition to form a fiber-loaded master batch having, for example, a final fiber content of about 50% by weight, or any other suitable amount; thereafter adding the fiber loaded master batch to the belt elastomer composition in order to allow for suitable distribution of the fiber in the belt elastomer composition; and then forming the belt with the thus fiber loaded elastomer composition via any suitable or conventional technique.
EXAMPLES
(33) In the following examples, inventive examples are indicated as Ex. And comparative examples as Comp. Ex.
(34) In a first set of examples, the rubber compositions are shown in volume percent in Table 1, and in phr in Table 2. Ex. 1 and Ex. 2 illustrate rubber compositions based on EOM elastomer with two different ratios of Kevlar pulp to para-aramid (1-mm chopped Technora) staple fiber. Comp. Ex. 3 is based on EPDM with similar fiber levels as Ex. 2, while Comp. Ex. 4 is based on CR elastomer. Note that the EPDM elastomer is Vistalon 2504, from Exxon, with a very low Mooney viscosity of about 25, and a broad molecular weight distribution, and includes about 10 phr of oil, all features intended to help with dispersing the high fiber loading. The EOM elastomer, on the other hand has a much higher Mooney viscosity of about 37, (indicating higher molecular weight), and practically no added oil, yet it was found that the EOM compositions were much easier to mix, mill and calender than the EPDM recipe.
(35) Compound testing results are shown in Table 3.
(36) Compound rheological properties were evaluated according to ASTM D-1646 on a Mooney viscometer with small rotor operated at 132? C. (270? F.) for 30 minutes (the Mooney Scorch results in Table 3. Also, Mooney viscosity was evaluated with large rotor at 125? C. Cure properties were evaluated according to ASTM D-5289 on a rotorless cure meter at 177? C. for 30 minutes and at 200? C. for 3 minutes. In Table 3, ML indicates minimum torque, MH indicates maximum torque, S is in-phase torque, and S is out-of phase torque. Based on MH, Ex. 1 with a preferred pulp level is the stiffest of these materials.
(37) Cured compound physical properties were also tested using standard rubber testing. The tensile test results in the with-grain direction in the low strain region are particularly interesting. Modulus was determined using common tensile modulus measurements, in accordance with ASTM D-412 (die C, and using 6/min. crosshead speed), and modulus (M5 and M10) herein refers to tensile stress at given elongation (5% and 10% respectively) as defined in ASTM D-1566 and ASTM D-412. Rubber hardness was tested on standard compression pellets with a durometer according to ASTM D-2240, using the Shore-A and Shore-D scales, for original and oven-aged compound samples. Tear results tested according to ASTM D-624, die-C, in two different directions, with-grain and cross-grain are included for some variables.
(38) It is apparent from the durometer and tensile properties that these are all very stiff, hard compositions, pushing the limits of what can be called flexible rubber for a belt. The with-grain elongation at break (% Eb) at room temperature is only about 15% for these materials, and the stress at 5% or 10% elongation (M5 and M10, respectively) is quite high. The with-grain properties are going to be directly related to the transverse stiffness of the CVT belt. However, the % Eb in the cross-grain direction, the direction for belt flexibility, is significantly larger. In fact, these compounds were intentionally selected to maximize transverse stiffness just within the limits of processability and cross-grain flexibility. The anisotropy ratio (based on either M5 or M10) is another indication of how well the compound should be able to flex in one direction while being extremely stiff in the other. While these four compounds have fairly similar anisotropy ratios, having been compounded to similar modulus or hardness, the inventive examples have significantly higher cross-grain % Eb, predicting much more flexibility in a belt than the comparative examples. The cross-grain tensile strength (Tb) of the inventive examples is also quite a bit higher than the comparative examples, both originally and after heat aging 168 hours at 150? C., attributable to the differences in elastomers. The with-grain tensile strengths are more comparable, attributable to the similarity in fiber loading and orientation. It is clear that the two Ex. materials have the highest M5 and M10 at room temperature (RT) in both grain directions. It is believed this leads directly to the high belt compression stiffness reported later herein, which in turn leads to outstanding performance in CVT use.
(39) It is desirable for the rubber composition for a CVT belt to have a tensile stress, in the mill direction (with-grain), at a strain of 5% of greater than or equal to 1800 psi, greater than or equal to 1900 psi, or greater than or equal to 2000 psi; and for the EOM compound to have an anisotropic ratio at a tensile strain of 5% of greater than or equal to 4, or greater than or equal to 4.5, or greater than or equal to 5. The use of EOM or EBM with both aramid pulp and aramid staple makes this possible.
(40) Table 3 includes the results of three abrasion tests for wear resistance, the so-called DIN test (DIN 53516 or ISO 4649), the PICO abrasion test (ASTM D-2228), and the Taber abrader test (ASTM D-3389). The DIN and Taber test results are in terms of volume loss, so lower is better. The PICO test is reported as an index, and a higher index indicates better resistance to abrasion. It can be seen that the abrasion resistance for the inventive examples are generally equivalent or sometimes better than the comparative examples, depending on which test and conditions.
(41) DeMattia flex crack growth test was according to ASTM D-430 (pierced) at RT and at 125? C., 0.5 stroke. Both with-grain and cross-grain were slated for test, but not all results were available for all compounds. At room temperature Ex. 1 is about an order of magnitude better than Comp. Ex. 3 and 4.
(42) Compound dynamic properties were evaluated according to ASTM D-6204 using temperature sweeps on the RPA2000 tester at 6.98% strain after curing the composition. The compound elastic modulus (G) results are shown in
(43) Note some observations on processing of the compounds. Comp. Ex. 4, based on CR elastomer with low Mooney viscosity and broad MW, has oil added to the composition, but still is quite difficult to process in terms of mixing and calendering without scorching the rubber. The sensitivity of CR to heat makes dispersing the fiber while maintaining adequate scorch safety very difficult. The improved heat resistance and processing of the ethylene elastomers is an advantage over CR. The comparative EPDM example used a 25 Mooney, broad molecular weight polymer with nearly 10 PHR of plasticizer to achieve adequate processing, whereas the ethylene-alpha-olefin used a 37 Mooney polymer but required no plasticizer in order to achieve good processing. By shifting the ratio of pulp to staple fiber, while adopting the unique properties of the ethylene-alpha-olefin or polyolefin elastomer, the modulus, as indicated by the compound MH provides a significantly improved level of stiffness in the resulting belt which has given exceptional durability and load carrying capabilities.
(44) Speculating further on the reasons for the improved compound performance observed (but with no intent to thereby limit the scope of the invention), one might infer from the higher Mooney viscosity of the EOM, a higher molecular weight polymer. Also, it is generally known that metallocene polymers can have narrower molecular weight distribution (MWD). Polymers with higher molecular weight and narrower MWD often give better physical properties.
(45) To summarize the conclusions from this first series of examples, the choice of EOM or other saturated polyolefin elastomer as the base elastomer, with a combination of aramid pulp and staple fiber at high total fiber loading and predetermined ratio of pulp to total fiber, results in ability to use higher-Mooney elastomer and less oil, giving a more polymer-rich composition, with better processing characteristics, higher cross-grain elongation or flexibility and strength at similar or higher with-grain modulus. Later, these effects will be shown to correlate with dramatic improvements in CVT belt performance.
(46) TABLE-US-00001 TABLE 1 Composition Comp. Comp. (Volume %) Ex. 1 Ex. 2 Ex. 3 Ex. 4 EOM (Engage 8180) 63.12% 63.35% EPDM (Vistalon 2504) 58.02% CR (Neoprene GW) 53.14% Para-aramid Pulp 3.35% 5.08% 5.10% 6.15% Para-Aramid Staple fiber 7.58% 6.44% 6.46% 4.23% Carbon Black 17.57% 16.94% 16.99% 21.87% Oil 0.19% 0.18% 5.44% 2.29% Antioxidant 0.48% 0.46% 0.46% 2.68% ZnO 0.27% 0.26% 0.26% Peroxide/coagent cure 7.43% 7.27% 7.27% package Resin/S-Cure package, 9.64% etc. Total Volume 100.00% 100.00% 100.00% 100.00% Pulp/Total Fiber (vol/vol) 30.6% 44.1% 44.1% 59.3%
(47) TABLE-US-00002 TABLE 2 Composition Comp. Comp. (phr) Ex. 1 Ex. 2 Ex. 3 Ex. 4 EOM (Engage 8180) 100.00 100.00 EPDM (Vistalon 2504) 100.00 CR (Neoprene GW) 100 Para-aramid Pulp 8.70 13.05 14.28 13.5 Para-aramid Staple fiber 19.01 16.53 18.10 9.0 Carbon Black 57.07 54.35 59.52 60 Oil 0.31 0.29 9.43 3.5 Antioxidant 0.92 0.87 0.95 4.3 ZnO 2.76 2.62 2.86 Peroxide/coagent cure package 19.88 19.21 21. Resin/S-Cure package, etc. 27.50 Total Parts 208.65 206.92 226.14 217.8 Pulp/Total Fiber (wt/wt) 31.4% 44.1% 44.1% 60.1%
(48) TABLE-US-00003 TABLE 3 Comp. Comp. (cont'd) Ex. 1 Ex. 2 Ex. 3 Ex. 4 Mooney Scorch (270? F.) MU Initial Vis. 185.39 156.77 156.96 130.58 Minimum Vis.(ML) 98.86 76.04 71.57 75.87 3 Pt Rise (t3) 9.73 11.65 8.56 5 Pt Rise (t5) 12.38 15.24 11.70 7.26 ML(1 + 4) 89.50 76.64 71.62 76.16 Mooney Viscosity 125? C. (ML1 + 4) MU ML 141.05 83.87 93.55 ML(1 + 4) 104.92 93.55 MDR 2000E (3 min.@ 200? C.) lb .Math. in MH 54.98 38.88 51.70 37.88 MH-ML 52.13 36.41 49.41 ML 2.85 2.47 2.29 4.57 Final S 54.87 38.75 51.70 42.45 Final S 3.06 2.66 4.37 3.61 Scorch2 0.21 0.27 0.23 0.31 T 99 (min) 1.95 1.70 2.31 2.71 Tan Delta final 0.06 0.07 0.08 0.09 MDR 2000E (30 min.@ 177? C.) lb .Math. in MH 64.15 47.46 55.45 32.79 MH-ML 61.08 44.97 53.76 ML 3.07 2.49 2.04 4.39 Final S 63.69 47.12 55.45 37.17 Final S 2.83 2.40 4.33 5.30 Scorch2 0.44 0.50 0.46 1.27 T 99 (min.) 13.16 13.43 13.89 28.06 Tan Delta final 0.04 0.05 0.08 0.14 Durometer Shore-A 95.81 95.33 92.00 Durometer Shore-D 56.03 53.44 53.33 Specific Gravity 1.17 1.15 1.18 1.41 Original Tensile Pull @ RT psi. WITH GRAIN % Eb 15.54 14.71 14.63 14.32 M5 2315.57 2184.36 1749.13 1419.61 M10 3427.39 3116.31 3173.05 2882.15 Tb 3624.92 3084.48 3317.44 3380.58 Break Energy C Tear lb/in kN/m 470 CROSS GRAIN % Eb 105.94 141.09 72.84 77.30 M5 435.88 399.26 265.00 317.80 M10 683.77 633.56 434.75 515.98 M20 1032.43 957.40 741.46 795.94 M25 1157.92 1067.48 868.83 898.17 M50 1499.06 1368.65 1269.05 1245.33 M100 1252.81 1616.81 Tb 1850.00 1707.97 1425.49 1479.36 Break Energy C Tear lb/in kN/m 246 Anisotropy Ratio at 5%, RT 5.34 5.47 6.60 4.47 Anisotropy Ratio at 10%, RT 4.95 4.92 7.30 5.59 Original Pull @ 125? C. psi. WITH GRAIN % Eb 12.06 12.50 9.03 M5 1014.12 1059.16 1261.06 M10 1492.92 1428.77 Tb 1637.76 1443.76 1666.93 Break Energy C Tear lb/in kN/m 151 CROSS GRAIN % Eb 59.68 55.65 38.53 M5 171.52 155.51 165.65 M10 304.17 262.75 292.91 M20 503.71 402.78 493.38 M25 577.20 451.26 563.75 M50 797.27 595.01 Tb 836.10 610.09 675.66 Break Energy C Tear lb/in kN/m 101 Anisotropy Ratio at 5%, 125? C. 5.91 6.81 7.61 Anisotropy Ratio at 10%, 125? C. 4.91 5.44 Oven Aged, 168 hr. 150? C. psi. - RT Durometer Shore-A 96.39 93.00 Durometer Shore-D 57.44 52.67 WITH GRAIN % Eb 14.74 14.28 11.49 M5 2527.34 2340.17 1800.03 M10 3648.84 3373.09 3832.05 Tb 4385.98 3399.88 4150.52 Break Energy C Tear lb/in kN/m 507 CROSS GRAIN % Eb 87.08 99.93 38.99 M5 500.76 454.48 489.68 M10 789.96 721.94 808.70 M20 1212.16 1096.60 1255.09 M25 1374.04 1218.12 1401.34 M50 1749.29 1535.91 M100 1944.49 1096.60 Tb 2127.53 1752.69 1647.62 Break Energy C Tear lb/in kN/m 268 Oven Aged, 168 hrs. 150? C. psi. Pulled at 125? C. WITH GRAIN % Eb 10.06 10.13 M5 1144.21 1240.02 M10 1924.78 1724.41 Tb 1890.06 1722.67 Break Energy C Tear lb/in 238 CROSS GRAIN % Eb 52.82 58.39 M5 168.94 178.88 M10 321.81 321.63 M20 544.26 519.49 M25 631.68 586.28 M50 882.77 653.05 Tb 846.56 805.90 Break Energy C Tear lb/in 101 Din Abrasion (cured 35 min. @ 350? F.) Horizontal Volume Loss (mm3) 130.93 138.40 161.97 Vertical Volume Loss (mm3) 107.87 94.60 101.00 Pico Abrasion Resistance 35 @ 350? F. RT Horizontal 111.07 85.60 71.74 RT Vertical 378.71 247.30 287.00 333.77 100? C. Horizontal 53.35 39.30 100? C. Vertical 97.71 64.80 40.70 Taber Abrader - Volume Loss (mm.sup.3) RT, Cycles (1000), Load Weight (1000 g), 212.42 268.20 213.60 248.78 Suction (70), H-18 RT, Cycles (2000), Load Weight (1000 g), 2.66 4.20 4.30 4.22 Suction (0), Round Cast Iron DeMattia Flex (pierced/0.5 stroke) [in./Mcycle] RT cross grain 56 511 307 125? C. cross grain 5888 511 3680 125? C. with grain 9200 [kcycle/inch] or [kcycle/2.54 cm] RT cross grain 53.38 2.54 3.26 125? C. cross grain 0.44 2.54 0.76
(49) In a second series of composition examples, four different polyolefin elastomers were compared in the same base recipe. The compositions, in phr, are shown in Table 4. The total fiber loading was about 28 phr and about 11 volume %. The amount of pulp was about 31% of the total fiber weight. The main purpose of this series was to evaluate processability, in terms of dispersion of ingredients in an internal mixer, handling on a two-roll mill, both of which were repeated three times. The results are indicated in Table 4 with + indicating very good handling and dispersion, o indicating ok or acceptable handling or dispersion, ? indicating not good handling on the mill and some undispersed ingredients out of the mixer, and ?? indicating poor processability. As indicated, some variables came out crumbly from the mixer, but generally could be brought together on the mill. The worst case exhibited a scaly surface, even after milling and three passes in the mixer. Clearly, with all other ingredients being equal, at these levels of fiber loading, EOM is the best, with EBM acceptable, EPM difficult but possible to use, and EPDM the most difficult to process.
(50) TABLE-US-00004 TABLE 4 Composition Comp. (phr) Ex. 5 Ex. 6 Ex. 7 Ex. 8 EOM (Engage 8180) 91.3 EBM (Exact 9061) 0 91.3 EPM (VISTALON V706) 0 91.3 EPDM (Nordel 3745) 0 91.3 Carbon Black 57.07 .fwdarw. .fwdarw. .fwdarw. 1-mm para-aramid staple 19.15 .fwdarw. .fwdarw. .fwdarw. 50% para-aramid pulp in 17.4 .fwdarw. .fwdarw. .fwdarw. EPDM masterbatch Antioxidant 0.92 .fwdarw. .fwdarw. .fwdarw. ZnO 2.76 .fwdarw. .fwdarw. .fwdarw. Paraffinic Oil 0.31 .fwdarw. .fwdarw. .fwdarw. Peroxide cure package 20.36 .fwdarw. .fwdarw. .fwdarw. Total Parts 209.27 .fwdarw. .fwdarw. .fwdarw. Pulp/Total Fiber (wt/wt) 31% .fwdarw. .fwdarw. .fwdarw. 1st pass in mixer + + crumbly crumbly on mill + brittle o ? 2d pass in mixer + o crumbly crumbly on mill + o o o 3d pass in mixer + + ? crumbly on mill + + ?scales ??scales overall processability + o ? ??
(51) Belt Examples and Test Results:
(52) In a first comparison, two belt embodiments, Belt A and Belt B are compared with two commercial CVT belts: Comp. Belt C, which is sold by Gates Corporation and Comp. Belt D, identified with part number 715000302. These belts all have pretty much the same dimensions as shown in Table 5, with nominal 31 mm top width, 952 mm length, and 26? V-angle. Comp. Belts C and D are heavier than Belts A and B due to the CR elastomer density being greater than EOM. Belt B was made with the same inventive materials as Belt A, but a little bit less rubber in the undercord portion of the belt, making Belt B a little thinner and lighter. Comp. Belts C and D are considered examples of highly optimized belts utilizing conventional rubber compositions.
(53) These belts were subjected to a number of tests designed to identify performance differences. These tests include a belt conditioning test lasting about six hours, followed by a Load Capability Test, Axial Stiffness Test, Bending Loss Test, and at the end of these tests (about 8 hours total), a Belt Weight Loss Test.
(54) The Belt Weight Loss Test results are shown in Table 5. The initial weight of the inventive belts is approximately 20% lower than the CR belts for the same belt size. Surprisingly, after the eight hours of performance testing, the wear of the inventive CVT belts was less than half of the wear of Comp. Belt D. A check of the final belt dimensions indicates a combination of wear on the sidewalls and permanent reduction in width from compression (indicated by a small increase in thickness).
(55) TABLE-US-00005 TABLE 5 Comp. Comp. Belt A Belt B Belt C Belt D.sup.1 Body Composition Ex. 1 Ex. 1 Comp. CR Ex. 4 Tensile cord aramid aramid aramid aramid Weight (g) 396.29 379.4 474.42 461.50 thickness (mm) 15.20 14.83 15.25 16.79 Pitch length (mm) 952 952 951 951 Belt Weight Loss Test (g) ?0.94 ?1.04 ?1.74 ?2.66 Width change (mm) ?0.52 ?0.51 ?0.96 ?0.77 Thickness change (mm) 0.07 0.08 0.12 0.07 .sup.1Comp. Belt D is a representative competitor's premium belt of unknown details, but believed to be CR elastomer with aramid tensile cord.
(56) The Load Capability Test is designed to simulate the conditions of the CVT belt drive with all significant phenomena encountered in the application. This test is carried out under a controlled, reproducible environment and measuring as many parameters as is practical, including speed loss, belt slip and belt axial deformation. In addition belt temperature is measured as it increases due to frictional and hysteretic energy losses. Test is conducted on an electric dynamometer simulating CVT belt under-drive conditions. During the test the speed of the driver shaft is constant at 1,500?1 rpm. Applied torque and hub load are varied. Test parameters are selected in such a way that some of the tested belts reach the extreme conditions: (1) belt temperature up to about 170? C.; or (2) excessive speed loss (up to 15% caused by belt slip and belt deformation in the sheaves).
(57) The Load Capability Test rig arrangement 500 is shown in
(58) The speed loss, s, is defined as percentage of change of the driven pulley speed, N.sub.n, due to a change in the load torque. It is calculated in reference to the driven pulley speed at zero torque, N.sub.no (no speed loss conditions) according to the following formulae:
(59)
(60) The speed loss is obtained by direct measurements of both shaft speeds. During the test the driver pulley speed is kept constant with precision of about 0.1%. The belt slip can also be determined from the speed loss and the measured belt pitch diameters.
(61) In the Load Capacity Test, Belts A and B show much better performance over the Comp. Belts C and D, as seen in
(62) In the Load Capacity Test, there is speed loss present at any load condition. As a result, the transfer of power, P, by the CVT drive is associated with a power loss, P.sub.s, due to the speed loss. It can be expressed by the formulae, P.sub.s=P?s %. The power loss results are shown in
(63) Finally, the Load Capacity Test pushed the belts beyond the torque levels of
(64) Table 6 includes a comparison of belt width change due to high torque load. This axial compression of the belt is one of the direct causes of speed losschange in belt width results in reduced pitch diameter of the belt in the driver and driven pulleys, which results in reduced speed ratio and speed loss. The inventive belts exhibit much less axial compression, a direct result of the increased transverse stiffness characteristics of the inventive rubber compositions. In addition, the strong performance of the thinner Belt B suggests the thickness can be advantageously reduced with the improved transverse properties of these rubber compositions. Thus, a thickness less than 15.0 mm may be advantageous. The cord position may also advantageously be adjusted to ride closer to the back surface or roots than to the underside surface or roots, as illustrated in
(65) TABLE-US-00006 TABLE 6 Comp. Comp. Belt A Belt B Belt C Belt D Speed loss at 100 Nm torque (%) 3.1 3.1 5.5 4.2 Speed loss at 120 Nm torque (%) 3.9 4.0 7.7 6.2 Speed loss at 145 Nm torque (%) 5.2 5.7 12.6 11.3 Belt Temperature at 100 Nm 83 79 103 96 torque (? C.) Belt Temperature at 120 Nm 96 93 126 118 torque(? C.) Belt Temperature at 145 Nm 117 116 171 159 torque (? C.) Belt width change at 145 Nm ?0.4 ?0.7 ?1.8 ?1.6 torque (mm)
(66) A Dynamic Axial Stiffness Test (DAST) was run on these four belts to see the direct influence of the rubber composition on the belt. As discussed above in the background section, belt change in width caused by belt compression under drive tension is one of the key characteristics of the belt because it influences the speed loss or speed ratio and energy loss in the CVT drive resulting in higher temperature and lower efficiency of the drive. The DAST explores the influence of the belt tension on the change in belt width. The test rig configuration is the same as used for the Load Capability Test (
(67) Belt axial stiffness is defined for the specific test configuration:
(68)
(69) Change in applied hub load, ?H, in the drive results in the change of belt width, ?W. The hub load force is recalculated into the axial (parallel to shaft axis) direction force component. It represents the pressure between belt and the pulley wall. Using the fact that the pulley groove angle A=26 degrees in this test gives the constant 2.17.
(70) For the purposes of the Dynamic Axial Stiffness Test, the belt is installed with driver pulley pitch diameter of 95?5 mm, speed ratio of 1.6?0.1, load torque of 30 Nm, and driver shaft speed of 1500 rpm. The initial hub load is set to H=3000?100 N, and the belt is run for about 30 minutes until the belt temperature is above 90? C., but not greater than 120? C. Belt radial position is recorded. Then hub load is gradually reduced to H=600 N, measuring belt radial position at each step. The reported axial stiffness is calculated from the belt width difference between 3000N and 600N using the above formula. The stiffness is the slope of the least squares best fit line through the H versus ?W data. The test can be done on belts of any width, in principle, but preferably the belt width ranges from 25 mm to 35 mm. Likewise, belt length should not affect the test very much. The test could also be scaled if necessary to evaluate very small or very large belts. For small belts, the hub load may be reduced, still providing a linear response region for determining the stiffness. For larger belts, the hub load values or range can be increased to provide for seating the belt in the pulleys and producing a suitable width reduction. Thus, hub load should be chosen as appropriate, related to the maximum application tension in the drive. At similar pitch diameter, belt size should not affect the transverse stiffness numbers much. However, if small diameter pulleys (or pitch line) is required for smaller belts, or larger diameter pulleys or pitch line for larger belts, then the stiffness would have to be adjusted for the difference in wrap distance in order to compare results with these ATV-size belts. The adjustment could be the equivalent of determining a modulus value instead of stiffness. More preferable is evaluating belt transverse stiffness using the compression test described later, at constant sample area and thickness.
(71) The summary of the DAST results is shown in Table 7. Thus, the belt rubber composition in Belts A and B leads directly to a decrease in width reduction, which is attributable to an increased axial stiffness of the belt, relative to the comparative belts. Belts A and B show a dynamic axial stiffness which averages about 75% higher than Comp. Belts C and D. This in turn leads to the performance improvements described earlier, namely lower belt running temperature, reduced radial slip, higher load capacity, and lower speed losses. In an application such as an ATV, this should lead to better acceleration, higher top speeds, lower belt temperatures, less fade, etc. This also should reduce the loss of power required to radially slide the belt into and out of the pulleys at the entrance and exit when belt is transitioning between the spans and inside the pulleys.
(72) In light of the results of the Dynamic Axial Stiffness Test and its correlation with CVT drive performance, it is advantageous that a rubber CVT belt exhibit a Belt Dynamic Axial Stiffness greater than 5.0 kN/mm or greater than 6.0 kN/mm or greater than 7.0 kN/mm, or from about 7 to about 8 kN/mm. It should be understood these numbers are based on the ATV belt sizes and test setup described herein, and may be transformed on a similar basis for other sizes of belts on other test setups.
(73) TABLE-US-00007 TABLE 7 Comp. Comp. Belt A Belt B Belt C Belt D Belt width reduction at H = 0.88 0.90 1.60 1.51 3 kN (mm) Belt Dynamic Axial Stiffness.sup.1 7.4 7.3 4.1 4.3 (kN/mm) .sup.1at 90? C. approximately.
(74) In light of the above results, a simpler axial stiffness test was devised based on ASTM D575-91 (reapproved in 2012), Test Method A, and called the Gates Compression Test (GCT) herein. The ASTM D575 method is used for compression measurements of elastomeric materials, using standard cylindrical buttons of 28.6?0.1 mm diameter, i.e., about 650 mm.sup.2 (1.000 in.sup.2) circular cross-sectional area and 12.5?0.5 mm (0.5 in) height. It is impossible to make such a sample from the CVT belts, so a length of belt is prepared as illustrated in
(75) The tests are conducted on a dynamic tensile machine using three samples cut from the same belt, measured separately. Also, the tests are run applying sinusoidal signal of displacement and recording force at the changing displacement. The test has been run at three different frequencies 2.5 Hz, 15 Hz and 30 Hz and at two values of temperature 23? C. and 90? C., although other conditions could be used. The frequency dependence was not very strong, so the 15 Hz results are used. The 90? C. temperature represents typical CVT belt operating range at high loads. The displacement range is based on the measured typical CVT belt axial deformation (i.e., compression) in the CVT drive pulleys under the relatively high, close-to-rated-load conditions for the applications, namely from 0.3 to 0.9 mm.
(76)
(77) Table 8 shows the test results for a collection of comparative belts found in the market, as well as the inventive Belt A. The four belts tested on both the GCT and DAST show a good correlation between the two tests, although the DAST values tend to be higher than the GCT values at the same temperature of 90? C. The difference could be the effect of friction force in the radial direction present between belt and sheave in the DAST. The inventive belt stands out from the pack with the highest stiffness on both tests. Thus, the GCT stiffness also correlates with CVT drive performance.
(78) In light of the results of the Gates Compression Test and its correlation with CVT drive performance, it is advantageous that a rubber CVT belt exhibit a Gates Compressive Test stiffness greater than or equal to 5.0 kN/mm at 90? C. or greater than 6.0 kN/mm or 7.0 kN/mm or 8 kN/mm at room temperature, or from about 8 to about 9 kN/mm at room temperature.
(79) TABLE-US-00008 TABLE 8 W GCT/23? C. GCT/90? C. DAST Ex. Description [mm] k [kN/mm] k [kN/mm] k [kN/mm] Belt A Inventive Belt A 33 8.6 5.0 7.4 Belt B Inventive Belt B 33 7.3 Comp. Belt C Gates CR-aramid cord 33 5.1 3.3 4.1 Comp. Belt D MBL BRP 715000302 33 3.7 3.0 4.3 Comp. Belt E MBL BRP 715900212 33 1.9 1.5 Comp. Belt F Huansong (Blue Label) 33 2.9 1.8 2113SS-305 Comp. Belt G Huansong (Bando) 33 3.1 3.1 911.531.528 Comp. Belt H Carlisle JD M168196 31 3.2 2.5 RSX-182 Comp. Belt I Gates CR-carbon cord 33 4.6 2.9 4.6 Comp. Belt J Huansong (Red Label) 33 3.7 2.4 2213SS-220 Comp. Belt K Scooter belt 22 4.4 3.7 EPDM-carbon cord Comp. Belt L Scooter belt 20 5.8 4.8 EPDM-polyester cord
(80) An additional test for the bending losses of a CVT Belt was carried out on belts A-D, herein called the Bending Loss Test (BLT). This test was able to separate two sources of loss, bending loss and radial friction loss. The BLT rig for measuring bending and radial friction losses in CVT Belts was similar in layout to the LCT rig described in
(81) The measured losses represent torque required to rotate the CVT belt in the simple drive with two small diameter pulleys with no resistance applied to the driven shaft. For simplicity, the torque losses measured at relatively low hub load are defined as belt bending losses, and the difference in torque losses due to an increase in hub load is defined as the frictional loss due to radial sliding.
(82) The results from the belt Bending Loss Test are two numbers: bending loss and radial friction loss. They are calculated as averages from the measured torque losses. In Table 9 there are test results for four belt constructions, three repeat tests for each value reported.
(83) The losses due to bending are about 20% higher for the inventive belts, which may be reflective of the higher modulus rubber compositions used. At the same time, the losses to overcome friction in radial sliding in and out of the pulley are approximately 40% lower, resulting in overall better efficiency on a CVT drive with the inventive belts.
(84) TABLE-US-00009 TABLE 9 Comp. Comp. Belt A Belt B Belt C Belt D Bending 59, 63, 55 51, 54, 51 50, 52, 46 51, 45, 49 Loss (Ncm) Friction 77, 83, 81 86, 83, 83 112, 107, 111 122, 113, 107 Loss (Ncm)
(85) In summary, they axial stiffness of inventive Belts A and B is approximately 70% higher than other belts, speed losses are lower at rated torque by 2% to 5%, and the losses due to bending are about 20% higher while the losses to overcome friction in radial sliding in and out of the pulley are approximately 40% lower, resulting in overall better performance on a CVT drive.
(86) The fiber-loaded rubber compositions described herein may have other applicability besides CVT belts. Other power transmission belts such as V-belts and multi-V-ribbed belts, which also benefit from high transverse stiffness could also be within the scope of the invention. Toothed or synchronous power transmission belts could also benefit from these compounding concepts, although the orientation effect therein would best be directed parallel to the belt running direction, at least in the teeth, which is the direction of maximum load on the teeth.
(87) Although the present invention and its advantages have been described in detail, it should be understood that various changes, substitutions, and alterations can be made herein without departing from the scope of the invention as defined by the appended claims. Moreover, the scope of the present application is not intended to be limited to the particular embodiments of the process, machine, manufacture, composition of matter, means, methods, and steps described in the specification. As one of ordinary skill in the art will readily appreciate from the disclosure of the present invention, processes, machines, manufacture, compositions of matter, means, methods, or steps, presently existing or later to be developed that perform substantially the same function or achieve substantially the same result as the corresponding embodiments described herein may be utilized according to the present invention. Accordingly, the appended claims are intended to include within their scope such processes, machines, manufacture, compositions of matter, means, methods, or steps. The invention disclosed herein may suitably be practiced in the absence of any element that is not specifically disclosed herein.