Patent Application
20180294069
Rubber is typically reinforced with various embodiments of textile, glass or steel fibers to provide basic strength, shape, stability, and resistance to bruises, fatigue, and heat. These fibers may be twisted into plies and cabled into cords. Rubber tires of various construction as well as various industrial products such as belts, hoses, seals, bumpers, mountings, and diaphragms can be prepared using such cords.
Manufacturers of rubber reinforced articles have long realized the importance of the interfacial adhesion of reinforcement of its rubber environment. Specialized coatings such as resorcinol/formaldehyde latex adhesives for polymeric cords and brass plating for steel cords are typically applied to fiber and wire reinforcements to enable them to function effectively for tire use. In addition, the compounds used to coat these reinforcements are usually specially formulated to develop adhesion. For example, many tire manufacturers use various cobalt salts as bonding promoters in their steel cord wire coats, as well as using relatively high ratios of sulfur to cure accelerator. The bonding promoters are added through compounding. To achieve a maximum bonding strength, an excess amount of cobalt salt is often added to the wire coat. Since only a very small portion of the cobalt salt may be engaged in the rubber-metal interfacial bonding reaction, most of the cobalt salts remained in the compound as excess cobalt without any contribution to the bonding. Cobalt is expensive and may even cause aging problems of the rubber when used in excess, as well as having objectionable environmental effects.
It continuously remains desirable to improve adhesion of reinforcement cords to rubber while simultaneously improving the properties of the coat compounds and reducing their cost.
The present invention is directed to a method of making a cord-reinforced rubber article, comprising the steps of
The invention is further directed to cord reinforced rubber articles made by the method.
The sole drawing is a schematic representation of one embodiment of the present invention.
There is disclosed a method of making a cord-reinforced rubber article, comprising the steps of
With reference now to the drawing, one embodiment of a method of treating a reinforcement cord according to the present invention is illustrated. In the process 10, carrier gas 18 from storage vessel 12 is directed to enter vaporizer vessel 14 wherein carrier gas 18 mixes with vaporized sulfur to form sulfur/carrier gas stream 15. Carrier gas 19, sulfur/carrier gas 15 and acetylene 17 from storage vessel 16 are mixed in-line to form gas mixture 21. Gas mixture 21 is sent to plasma generator 22, where atmospheric plasma 24 is generated from gas mixture 21. Reinforcement cord 26 is unwound from spool 30 and conveyed through plasma generator 22 and atmospheric plasma 24 for deposition of a polymerized coating by the plasma 24. Treated reinforcement cord 28 exits plasma generator 22 and is wound onto spool 32 for storage.
The plasma generator may be any suitable plasma generation device as are known in the art to generate atmospheric pressure plasmas, such as atmospheric pressure plasma jet, atmospheric pressure microwave glow discharge, atmospheric pressure glow discharge, and atmospheric dielectric barrier discharge. In one embodiment, the plasma generator is of the dielectric barrier discharge type. The dielectric barrier discharge apparatus generally includes two electrodes with a dielectric-insulating layer disposed between the electrodes and operate at about atmospheric pressures. The dielectric barrier discharge apparatus does not provide one single plasma discharge, but instead provides a series of short-lived, self-terminating arcs, which on a long time scale (greater than a microsecond), appears as a stable, continuous, and homogeneous plasma. The dielectric layer serves to ensure termination of the arc. Further reference may be made to U.S. Pat. No. 6,664,737 for its teaching regarding the operation of a dielectric barrier discharge apparatus. Suitable configurations for treatment of substrates using atmospheric plasmas are known, for example, in U.S. Pat. Nos. 9,255,330 and 8,927,052 and U.S. Publications 2010/0028561, 2009/0148615, and 2007/0202270.
By atmospheric pressure plasma, it is meant that the pressure of the plasma is equal to or slightly above the ambient pressure of the surroundings.
The gas mixture includes a carrier gas, sulfur and an alkyne.
Suitable alkynes C2 to C10 alkynes such as acetylene, propyne, 1-butyne, 2-butyne, 1-pentyne, 2-pentyne, 3-methylbut-1-yne, 1-hexyne, 2-hexyne, 3-hexyne, 3,3-dimethylbut-1-yne, 1-heptyne and isomers, 1-octyne and isomers, 1-nonyne and isomers, and 1-decyne and isomers. In one embodiment, the alkyne is acetylene.
In one embodiment, sulfur is introduced in the form of a vaporized elemental sulfur. The vaporization process for sulfur may consist of a heated vessel with heat generation sufficient to melt and vaporize the elemental sulfur, in one embodiment, the vaporized sulfur may be swept from the heated vessel using carrier gas identical to that used in the plasma generator, for example, by bubbling carrier gas such as argon through the molten sulfur in the heated chamber and carry vaporized sulfur through an exit port in the heated chamber. The vaporized sulfur/argon stream is then directed to the plasma chamber, along with the acetylene and carrier gas.
Suitable carrier gas includes any of the noble gases including helium, argon, xenon, and neon. Also suitable as carrier gas are nitrogen, carbon dioxide, nitrous oxide, carbon monoxide, and air. In one embodiment, the carrier gas is argon.
In one embodiment, the sulfur and alkyne are present in a volume ratio sulfur/alkyne in a range of from 0.07 to 0.7. In one embodiment, the sulfur and alkyne are present in a volume ratio sulfur/alkyne in a range of from 0.15 to 0.45.
In one embodiment, the sulfur and alkyne are present in a volume ratio (sulfur+alkyne)/carrier gas in a range of from 0.001 to 0.1. In one embodiment, the sulfur and alkyne are present in a volume ratio (sulfur+alkyne)/carrier gas in a range of from 0.005 to 0.025.
The tire cord is constructed of any of the various reinforcement materials commonly used in tires. In one embodiment, the tire cord includes steel and polymeric cords. Polymeric cords may include any of the various textile cords as are known in the art, including but not limited to cords constructed from polyamide, polyester, polyketone, rayon, and polyaramid. In one embodiment, the reinforcement cord includes steel, galvanized steel, zinc plated steel and brass plated steel.
The atmospheric pressure plasma treated cord may be used in a component of a pneumatic tire. The treated cord is calendered or otherwise contacted with a rubber composition to form the tire component using procedures as are known in the art. In various embodiments, the tire component may be a belt, carcass, apex, bead, chipper, flipper, or any other component including a cord reinforcement as are known in the art. In one embodiment, the tire component is a steel belt wherein treated steel reinforcement cords are calendared into a rubber composition.
The rubber composition to be contacted with the treated reinforcement cord includes one or more rubbers or elastomers containing olefinic unsaturation. The phrases “rubber or elastomer containing olefinic unsaturation” or “diene based elastomer” are intended to include both natural rubber and its various raw and reclaim forms as well as various synthetic rubbers. In the description of this invention, the terms “rubber” and “elastomer” may be used interchangeably, unless otherwise prescribed. The terms “rubber composition,” “compounded rubber” and “rubber compound” are used interchangeably to refer to rubber which has been blended or mixed with various ingredients and materials and such terms are well known to those having skill in the rubber mixing or rubber compounding art. Representative synthetic polymers are the homopolymerization products of butadiene and its homologues and derivatives, for example, methylbutadiene, dimethylbutadiene and pentadiene as well as copolymers such as those formed from butadiene or its homologues or derivatives with other unsaturated monomers. Among the latter are acetylenes, for example, vinyl acetylene; olefins, for example, isobutylene, which copolymerizes with isoprene to form butyl rubber; vinyl compounds, for example, acrylic acid, acrylonitrile (which polymerize with butadiene to form NBR), methacrylic acid and styrene, the latter compound polymerizing with butadiene to form SBR, as well as vinyl esters and various unsaturated aldehydes, ketones and ethers, e.g., acrolein, methyl isopropenyl ketone and vinylethyl ether. Specific examples of synthetic rubbers include neoprene (polychloroprene), polybutadiene (including cis 1,4 polybutadiene), polyisoprene (including cis 1,4 polyisoprene), butyl rubber, halobutyl rubber such as chlorobutyl rubber or bromobutyl rubber, styrene/isoprene/butadiene rubber, copolymers of 1,3 butadiene or isoprene with monomers such as styrene, acrylonitrile and methyl methacrylate, as well as ethylene/propylene terpolymers, also known as ethylene/propylene/diene monomer (EPDM), and in particular, ethylene/propylene/dicyclopentadiene terpolymers. Additional examples of rubbers which may be used include alkoxy-silyl end functionalized solution polymerized polymers (SBR, PBR, IBR and SIBR), silicon-coupled and tin-coupled star-branched polymers. The preferred rubber or elastomers are polyisoprene (natural or synthetic), polybutadiene and SBR.
The rubber composition to be contacted with the treated reinforcement cord may include at least one of methylene donors and methylene acceptors.
In one embodiment, the methylene donor is an N-substituted oxymethylmelamines, of the general formula:
wherein X is hydrogen or an alkyl having from 1 to 8 carbon atoms, R1 R2, R3, R4 and R5 are individually selected from the group consisting of hydrogen, an alkyl having from 1 to 8 carbon atoms, the group —CH2OX or their condensation products. Specific methylene donors include hexakis-(methoxymethyl)melamine, N,N′,N″-trimethyl/N,N′,N″-trimethylolmelamine, hexamethylolmelamine, N,N′,N″-dimethylolmelamine, N-methylolmelamine, N,N′-dimethylolmelamine, N,N′,N″-tris(methoxymethyl)melamine, N,N′N″-tributyl-N,N′,N″-trimethylol-melamine, hexamethoxymethymelamine, and hexaethoxymethylmelamine. In one embodiment, the N-substituted oxymethylmelamine is hexamethoxymethylmelamine. The N-methylol derivatives of melamine are prepared by known methods.
The amount of N-substituted oxymethylmelamine in the rubber composition may vary. In one embodiment, the amount of N-substituted oxymethylmelamine ranges from 0.5 to 4 phr. In another embodiment, the amount of N-substituted oxymethylmelamine ranges from 1 to 3 phr. The N-substituted oxymethylmelamine may be added as the free compound, or dispersed on a carrier medium such as silica.
In one embodiment, the rubber composition includes a methylene acceptor. The term “methylene acceptor” is known to those skilled in the art and is used to describe the reactant to which a methylene donor reacts to form what is believed to be a methylol monomer. The condensation of the methylol monomer by the formation of a methylene bridge produces the resin. The initial reaction that contributes the moiety that later forms into the methylene bridge is the methylene donor wherein the other reactant is the methylene acceptor. Representative compounds which may be used as a methylene acceptor include but are not limited to resorcinol, resorcinolic derivatives, monohydric phenols and their derivatives, dihydric phenols and their derivatives, polyhydric phenols and their derivatives, unmodified phenol novolak resins, modified phenol novolak resin, resorcinol novolak resins and mixtures thereof. Examples of methylene acceptors include but are not limited to those disclosed in U.S. Pat. No. 6,605,670; U.S. Pat. No. 6,541,551; U.S. Pat. No. 6,472,457; U.S. Pat. No. 5,945,500; U.S. Pat. No. 5,936,056; U.S. Pat. No. 5,688,871; U.S. Pat. No. 5,665,799; U.S. Pat. No. 5,504,127; U.S. Pat. No. 5,405,897; U.S. Pat. No. 5,244,725; U.S. Pat. No. 5,206,289; U.S. Pat. No. 5,194,513; U.S. Pat. No. 5,030,692; U.S. Pat. No. 4,889,481; U.S. Pat. No. 4,605,696; U.S. Pat. No. 4,436,853; and U.S. Pat. No. 4,092,455. Examples of modified phenol novolak resins include but are not limited to cashew nut oil modified phenol novolak resin, tall oil modified phenol novolak resin and alkyl modified phenol novolak resin. In one embodiment, the methylene acceptor is resorcinol.
Other examples of methylene acceptors include activated phenols by ring substitution and a cashew nut oil modified novolak-type phenolic resin. Representative examples of activated phenols by ring substitution include resorcinol, cresols, t-butyl phenols, isopropyl phenols, ethyl phenols and mixtures thereof. Cashew nut oil modified novolak-type phenolic resins are commercially available from Schenectady Chemicals Inc. under the designation SP6700. The modification rate of oil based on total novolak-type phenolic resin may range from 10 to 50 percent. For production of the novolak-type phenolic resin modified with cashew nut oil, various processes may be used. For example, phenols such as phenol, cresol and resorcinol may be reacted with aldehydes such as formaldehyde, paraformaldehyde and benzaldehyde using acid catalysts. Examples of acid catalysts include oxalic acid, hydrochloric acid, sulfuric acid and p-toluenesulfonic acid. After the catalytic reaction, the resin is modified with the oil.
The amount of methylene acceptor in the rubber stock may vary. In one embodiment, the amount of methylene acceptor, if used, ranges from 0.5 to 5 phr. In another embodiment, the amount of methylene acceptor, if used, ranges from 1 to 3 phr.
In one embodiment, the rubber composition excludes a methylene acceptor. In one embodiment, the rubber composition excludes resorcinol.
It is readily understood by those having skill in the art that the rubber compositions used in tire components would be compounded by methods generally known in the rubber compounding art, such as mixing the various sulfur-vulcaniza.bile constituent rubbers with various commonly used additive materials such as, for example, curing aids, such as sulfur, activators, retarders and accelerators, processing additives, such as oils, resins including tackifying resins, silicas, and plasticizers, fillers, pigments, fatty acid, zinc oxide, waxes, antioxidants and antiozonants, peptizing agents and reinforcing materials such as, for example, carbon black. As known to those skilled in the art, depending on the intended use of the sulfur vulcanizable and sulfur vulcanized material (rubbers), the additives mentioned above are selected and commonly used in conventional amounts.
The rubber compound may contain various conventional rubber additives. In one embodiment, the addition of carbon black comprises about 10 to 200 parts by weight of diene rubber (phr). In another embodiment, from about 20 to about 100 phr of carbon black is used.
A number of commercially available carbon blacks may be used. Included in, but not limited to, the list of carbon blacks are those known under the ASTM designations N299, N315, N326, N330, N332, N339, N343, N347, N351, N358, N375, N539, N550 and N582. Such processing aids may be present and can include, for example, aromatic, naphthenic, and/or paraffinic processing oils. Typical amounts of tackifying resins, such as phenolic tackifiers, range from 1 to 3 phr. Silica, if used, may be used in an amount of about 5 to about 100 phr, often with a silica coupling agent. Representative silicas may be, for example, hydrated amorphous silicas. Typical amounts of anti oxi dants comprise about 1 to about 5 phr. Representative antioxidants may be, for example, diphenyl-p-phenylenediamine, polymerized 1,2-dihydro-2,2,4-trimethylquinoline and others, such as, for example, those disclosed in the Vanderbilt Rubber Handbook (1990), Pages 343 through 362. Typical amounts of antiozonants comprise about 1 to about 5 phr. Representative antiozonants may be, for example, those disclosed in the Vanderbilt Rubber Handbook (1990), Pages 363 through 367. Typical amounts of fatty acids, if used, which can include stearic acid comprise about 0.5 to about 3 phr. Typical amounts of zinc oxide comprise about 2 to about 10 phr. Typical amounts of waxes comprise about 1 to about 5 phr. Often microcrystalline waxes are used. Typical amounts of peptizers comprise about 0.1 to about 1 phr. Typical peptizers may be, for example, pentachlorothiophenol and dibenzamidodiphenyl disulfide.
The vulcanization is conducted in the presence of a sulfur vulcanizing agent. Examples of suitable sulfur vulcanizing agents include insoluble sulfur, elemental sulfur (free sulfur) or sulfur donating vulcanizing agents, for example, an amine disulfide, polymeric polysulfide or sulfur olefin adducts. In one embodiment, the sulfur vulcanizing agent is elemental sulfur. In one embodiment, sulfur vulcanizing agents are used in an amount ranging from about 0.5 to about 8 phr. In another embodiment about 3 to about 5 phr of sulfur vulcanizing agents are used.
Accelerators are used to control the time and/or temperature required for vulcanization and to improve the properties of the vulcanizate. In one embodiment, a single accelerator system may be used, i.e., primary accelerator. Conventionally, a primary accelerator is used in amounts ranging from about 0.5 to about 2.5 phr. In another embodiment, combinations of two or more accelerators may be used, including a primary accelerator which is generally used in the larger amount (0.5 to 2.0 phr), and a secondary accelerator which is generally used in smaller amounts (0.05 to 0.50 phr) in order to activate and to improve the properties of the vulcanizate. Combinations of these accelerators have been known to produce a synergistic effect of the final properties and are somewhat better than those produced by use of either accelerator alone. In addition, delayed action accelerators may be used which are not affected by normal processing temperatures but produce satisfactory cures at ordinary vulcanization temperatures. Suitable types of accelerators that may be used in the present invention are amines, disulfides, guanidines, thioureas, thiazoles, thiurams, sulfenamides, dithiocarbamates and xanthates. In one embodiment, the primary accelerator is a sulfenamide. In another embodiment, if a second accelerator is used, the secondary accelerator may be a guanidine, dithiocarbamate, thiuram, or a second sulfenamide.
The tire containing the tire component can be built, shaped, molded and cured by various methods which will be readily apparent to those having skill in such art.
The prepared tire of this invention is conventionally shaped and cured by methods known to those having skill in such art.
While the invention as described herein has been directed to tire cords and tires, the method is not so limited. Other applications of reinforcement cords, which includes tire cords, as treated by the methods described herein can be envisioned. Any rubber or elastomer article of manufacture reinforced with reinforcement cords can utilize cords as treated by the methods described herein. For example, applications of the treated reinforcement cords using the plasma methods described herein include reinforced hoses, transmission belts, drive belts, air springs, conveyor belts, drive tracks, and the like. Thus, the methods as described herein as suitable for treatment of tire cords are equally applicable to the treatment of any reinforcement cord as used in reinforced rubber or elastomer articles of manufacture.
The invention is further described with reference to the following examples.
In this example, the effect of using elemental sulfur and acetylene in an atmospheric plasma to coat zinc-plated steel reinforcement cords is illustrated. A laboratory dielectric barrier discharge apparatus was constructed consisting of a quartz tube with an aluminum tape electrode wrapped on the exterior of the tube and connected to a high voltage power supply. The steel cord was connected to the ground. Argon gas at atmospheric pressure mixed with vaporized sulfur and acetylene was passed through the interior of the quartz tube. A steel tire cord of 4+3×0.35 UT Zinc-plated construction was extended through the interior of the quartz tube and held stationary. Application of high voltage to the aluminum tape electrode ignited a plasma in the quartz tube.
The process was modified to enable the vaporization of high-boiling chemicals into the plasma reactor without vapor condensation.
The sulfur vaporization process consisted of an aluminum heating mantle (evaporator) into which a Pyrex vial containing elemental sulfur was inserted. The Pyrex vial was equipped with a side port for the injection of a gentle stream of argon carrier gas to push the vaporized chemical into the plasma reactor tube. The aluminum mantle was wrapped with heating wire connected to a dual-channel temperature controller. The temperature was steadily controlled via a thermocouple inserted in a well drilled in the sidewall of the evaporator. Temperatures up to 350° C. could be reached in the vial. The use of an aluminum well had the advantage of lowering the temperature gradient applied to the glass as well as to create thermal inertia to help stabilize the temperature.
The Pyrex vial was made based on the principle of a bubbler. The argon gas stream into the vial was directed towards the bottom of the vial via a capillary plunger tube. Due to the high temperatures, quartz was also considered as a material to custom-make the vial but successful heating trials on a Pyrex vial were conclusive.
Additionally, to prevent high-temperature vapors from condensing in the main reactor tube, a second independently-controlled heating zone was placed on the tubular reactor, almost up to the plasma zone. To prevent arcing between the high voltage and the heating wire, the section of the heating zone closest to the plasma was wrapped with insulating polyimide tape. The temperature of the second heating zone was set 10° C. higher compared to the vial temperature to prevent condensation. The temperature of this second heating zone was controlled via a thermocouple inserted between the heating wire and the tubular reactor.
Argon and acetylene were introduced in the tubular reactor and traveled through the heated section of the tubular reactor (2nd zone). Further dilution of the sulfur vapor in the blend of acetylene and argon occurred before reaching the plasma zone.
A series of experiments exposing a zinc-plated steel cord to a plasma was performed, using various power input to electrode, various exposure times of the steel cord to the plasma, and various argon gas flow rates into the quartz tube. The resulting plasma treated steel cords were embedded to a depth of 12.7 mm into a standard rubber wirecoat compound for passenger tires and cured at 155° C. for 35 minutes. Each cured wire/rubber sample was then tested for adhesion using a tire cord adhesion test (TCAT) following procedures given in Nicholson et al, Tire Science and Technology, TSTCA, Vol. 6, No. 2, May 1978, pp. 114-124. The results of these pull-out tests (TCAT) and percent rubber coverage are given in Table 1.
Initial screening experiments were conducted using elemental sulfur and acetylene. Zinc-plated 4+3×0.35 UT steel cord was used for this study. The wire was used as received without further cleaning. Plasma coated wires were directly cured in a tire cord adhesion test (TCAT) geometry (½″, 35 min @ 310 F) using cobalt-free rubber wirecoat compounds to measure pull-out forces and rubber coverages. Results are from an average of four pulls. The elemental sulfur was purchased from Sigma-Aldrich with a purity of 99.5-100%.
Table 1 below presents plasma processing conditions as well as rubber adhesion data for this initial set of experiments.
The data of Table 1 was analyzed using SAS JMP statistical analysis software to determine the parameters that have the most influence on adhesion. The model below shows a strong correlation between adhesion and line speed and predicts an optimum around 5.5 V for the wind-up voltage. Indeed, the grafting of the coating to the zinc plating, most likely through initial zinc sulfidation as well as the coating thickness depend on the line speed. The model also predicts a strong correlation between the Argon gas flow through the vial and the evaporator temperature, indicating the importance of the amount of sulfur vapor introduced into the plasma reactor. An optimum in sulfur vapor concentration may depend on the total Argon gas flow rate through the reactor. Surprisingly, the plasma power was found to have no influence on the resulting adhesion to the plasma coated wire.
In this example, the quantification of sulfur vapor output into the tubular reactor is illustrated.
As data of the above Table 1 indicate a strong correlation between the argon flow rate through the vial and the evaporator temperature, it was desired to determine the quantity of sulfur vapor delivered to the plasma zone and determine how to control this flow of vapor. For this calculation, the heated vial containing the sulfur was assimilated to a bubbler.
Assuming all gases to be ideal, the mole fractions of sulfur vapor and argon carrier gas have the same ratio as their partial pressures. Additionally, the partial pressure of the argon carrier gas is assumed equal to the difference between the pressure in the bubbler headspace (1 atmosphere) and the equilibrium pressure of the vapor.
From the ideal gas law, Cv=Pv/Pt and also Cv=Qv/(Qc+Qv) when taking into account the flow rates with:
The flow rate of sulfur vapors exiting the bubbler can then be deducted by combining both above equations:
Qv=Qc×Pv/(Pt−Pv)
The vapor pressure of elemental Sulfur at different temperatures was found from West et al., Reference.
Table 2 provides an approximation of calculated sulfur vapor flow exiting the vial for different temperatures and argon carrier gas flow rates. Results in Table 5 highlight the importance of the correlation between temperature and argon flow rate through the vial. It can be concluded that a control over the amount of sulfur vapor injected into the reactor can be achieved by tuning the temperature and argon flow rate.
To further develop the plasma coating process for elemental sulfur/acetylene, a definitive screening design was performed. This type of design was chosen to limit the number of experiments to run as well as to avoid confounding of effects since this system features at least an active two-factor interaction between the evaporator temperature and argon gas flow rate through the vial.
The following experimental conditions were used for this Design of Experiments: Zinc-plated 4+3×0.35 UT steel cord was used as received without further cleaning. Plasma coated wires were directly cured in a tire cord adhesion test (TCAT) geometry (½″, 35 min @ 310 F) using cobalt-free compound 1 as well as cobalt-free compound 2 to measure pull-out forces and rubber coverages. Four TCAT samples were cured and pulled for each experiment.
Table 3 below presents the generated data as well as the corresponding TCAT adhesion results for both compounds. Experiments 10 & 11 are additional conditions that were added to the definitive screening design.
From the data of Table 4 the wind-up speed was found to be the most significant parameter. The wind-up speed had a strong impact on the thickness of the deposited coating and it is known that adhesion promoting interphases typically exhibit an optimum thickness for which adhesion is maximal. For this system, the slower the winding speed, the thicker the coating. However, the impact of the composition of the coating on adhesion is not reflected in the above model since the deposited coating results from a co-polymerization of two precursors with variable concentrations. Therefore, to further understand the importance of the chemistry of the coating, an additional model was built which takes into account the contribution of sulfur, acetylene as well as the residence time of the gases in the plasma zone.
To shed light on the importance of the coating chemistry, the following parameters were calculated and used as variables:
Although the winding speed is not part of this analysis, it is intrinsically contained in the first two parameters since it was used to calculate the quantities of sulfur and acetylene. The quantity of sulfur was calculated from the above bubbler model and winding speed, while the residence time was obtained by taking into account the flow rates, tube inner diameter and cord diameter.
The above parameters were calculated and consigned in the Table 4 below. From Tables 3 and 4, a significant effect on adhesion is observed for the quantity of sulfur vapor flowing through the reactor during the time it takes for any single area of the wire to fully cross the plasma zone. The same analysis for the quantity of acetylene shows a marginal significance while the residence time of the gases in the plasma zone is not significant at all within the chosen design space. These results underlines the importance of the coating chemistry since best rubber adhesion was obtained using a low flow of sulfur vapor and an intermediate amount of acetylene, although the latter parameter is of lesser importance. Ideally, the concentration of sulfur in the plasma coating should be close to the one in the compound to increase the affinity between the coating and the compound during vulcanization. Without wishing to be bound by any theory, it is postulated that the role of acetylene, beyond diluting the sulfur and improving the processing speed is to create a stronger and more stable carbon/sulfur network and to potentially participate to the vulcanization process via C═C double bonds created during the plasma polymerization of acetylene.
In this example, the effect of various aging conditions on adhesion of plasma treated tire cords is illustrated. Original and aged adhesion in wire coat compound were determined for wires that were plasma coated respectively with sulfur/acetylene according to the three selected processing conditions as well as wires that were plasma coated with carbon disulfide/acetylene using typical coating conditions. Adhesion of 4−3×0.35 UT Brass reference in a cobalt free wirecoat compound as well as a cobalt-containing wirecoat compound is also reported for comparison purposes.
Zinc electroplated 4+3×0.35 UT steel cord was used, following the treatment procedure described in Example 1.
Processing parameters for hree selected elemental Sulfur/Acetylene plasma coating conditions are given in Table 5.
Table 6 summarizes the processing conditions used for the plasma coating deposition of a blend of carbon disulfide and acetylene on zinc-plated steel cords for comparison.
Elemental Sulfur was purchased from Sigma-Aldrich with a purity of 99.5% -100.5% Plasma coated wires as well as reference Brass steel cords were cured in TCAT blocks featuring an embedment length of ¾″ (19 mm) in two wirecoat compounds, the first cobalt-free and second containing cobalt.
The following suite of TCAT block aging conditions was selected to determine the impact on wire pull-out force and coverage:
The following cure conditions were selected to assess the effect of cure temperature on adhesion:
The following conclusions can be drawn in light of the above results:
| Number | Date | Country | |
|---|---|---|---|
| 62435910 | Dec 2016 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15846808 | Dec 2017 | US |
| Child | 16006132 | US |
