This application claims priority benefit of Serial No. 20215194, filed Feb. 23, 2021 in Finland, and which application is incorporated herein by reference. To the extent appropriate, a claim of priority is made to the above-disclosed application.
The invention concerns the way in which a pneumatic tire is made self-sealing for a case of puncture happening in use. The invention concerns a method for manufacturing such self-sealing sealant layer to a pneumatic tire.
In pneumatic tires for cars, a puncture caused by a sharp object hitting the tire has been a problem since the beginning of use of pneumatic tires. It is known from various patents that a puncture can be sealed by providing a suitable sealing agent to stick to the object causing the puncture. Thus, when the object is removed from the punctured tire, the sealing agent fills the puncture and prevents the pressurized gas from escaping from the tire. Methods for applying sealing agent are known e.g. from the patent applications EP 0 080 968 and EP 0 161 201. The sealing agent may be applied in a form of a premanufactured strip. Alternatively, as shown in
Typically, the material used as sealing agent 200 is sticky and viscous, whereby its application may be problematic. Typically, the sealing agent is heated to at least 70 degrees Celsius to enable application thereof. Heating may e.g. reduce viscosity. However, heating of the sealing agent, in connection with a temperature dependent viscosity, makes an even application of the sealing agent reasonably problematic.
It has been found that by using a two-component or multi component sealing agent the problems of prior art can be avoided or reduced. The two components of the sealing agent are a base elastomer and a curing agent. In case of a multi-component sealing agent, some components thereof may constitute the base elastomer and some components may constitute the curing agent. Only when the components, i.e. the base elastomer and the curing agent, are mixed together to form the sealing agent, the vulcanization (i.e. curing) of the sealing agent starts, whereby the sealing agent is workable for some time. The workable time of the sealing agent is referred to as a pot life of the sealing agent. Thus, during the pot life of the sealing agent, the sealing agent may be applied to the pneumatic tire, and it needs not be heated. To ensure application during the pot life and to avoid clogging of the extrusion device, the base elastomer and the curing agent are extruded using separate extrusion devices, and the throughputs of the extrusion devices are mixed to obtain the sealing agent. In contrast, if a pre-mixed composition of the sealing agent would be applied as indicated in
The invention is described in more detail in independent claim 1. Dependent claims and the description define preferable embodiments.
The pneumatic tire 100 comprises a first sidewall 122 and a second sidewall 124. Typically, the pneumatic tire 100, e.g. the carcass 105 thereof, comprises an innerliner 130, which is configured to decrease air permeability of the pneumatic tire 100 (i.e. improve its air tightness). For manufacturing reasons, a layer of inside tire paint may be arranged on the innerliner 130. The innerliner 130, optionally with a layer of the inside tire paint, may be arranged as an innermost layer of the pneumatic tire. The pneumatic tire 100 comprises an inner surface 102. At least a part of the inner surface 102 may be formed by the innerliner 130. In case the innerliner 130 is covered with inside tire paint that is not removed, at least a part of the inner surface 102 may be formed by the inside tire paint, as detailed below.
As indicated in background, the inner surface 102 of the pneumatic tire 100 may be provided with sealing agent 200, i.e. self-sealing agent. For clarity,
To allow for workability of the sealing agent 200, in the embodiments of the present invention, a two-component sealing agent 200 or a multi component sealing agent 200 is used. The two components are (i) a base elastomer and (ii) a curing agent. As detailed below, the base elastomer may be a mixture of some compounds of a multi component sealing agent. As detailed below, the curing agent may be a mixture of some compounds of a multi component sealing agent. Thus, the sealing agent may comprise also other components. The sealing agent is formed by mixing at least these two components. Neither the base elastomer nor the curing agent alone starts to cross link. However, when mixed together, the curing agent starts and/or accelerates the vulcanization process of the sealing agent, whereby the sealing agent needs to be applied onto the tire reasonably soon after mixing the two components. If the already mixed sealing agent was extruded by only one extruder 300 (as in
With reference to
With reference to
Even if not shown, it is possible that (i) the base elastomer and the first throughput 210 thereof are formed by mixing the primary first throughput 210a and the secondary first throughput 210b, and (ii) the curing agent and the second throughput 220 thereof are formed by mixing the primary second throughput 220a and the secondary second throughput 220b.
Referring to
Moreover, it is noted that when all the partial (or full) throughputs are mixed at the same point, it may be immaterial whether a component is considered to form a part of the first throughput 210 or the second throughput 220. For example, referring to
Referring to
As indicated in
The base elastomer as such is configured not to vulcanize (i.e. cure), or vulcanize only very slowly. Thus, a pot life of the base elastomer may be e.g. at least one month at room temperature. The term shelf life can be used instead of the term pot life, because the base elastomer is configured to be stored for a long period without curing. In a similar manner, the curing agent as such is configured not to vulcanize (i.e. cure), or vulcanize only very slowly. Thus, a pot life of the curing agent may be e.g. at least one month at room temperature. The term shelf life can be used instead of the term pot life, because the curing agent is configured to be stored for a long period without curing.
Instead, a pot life of the sealing agent 200 is much shorter than the pot life of either of the base elastomer and the curing agent. This is because the curing agent, when mixed with the base elastomer, is configured to accelerate vulcanization of the sealing agent 200. The pot life of the sealing agent 200 may be e.g. from 5 minutes to 45 minutes at room temperature. Correspondingly, the pot life of the base elastomer may be at least two hundred times the pot life of the sealing agent 200; and the pot life of the curing agent may be at least two hundred times the pot life of the sealing agent 200. A definition for the pot life is the time that it takes, from the mixing, to increase the viscosity of the sealing agent from its initial value by 100%.
In an embodiment, the base elastomer, the curing agent, and the mass flow ratio of the second throughput to the first throughput (hereinafter a mixing ratio) is selected such that a pot life of the sealing agent 200 is from 5 minutes to 45 minutes at room temperature. Typically, a manufacturer of a two-component sealing agent provides, separately, the base elastomer and the curing agent, and also indicates a preferred mixing ratio and the obtainable pot life. A two-component sealing agent for the invention may be arranged available accordingly. By varying the mixing ratio, the pot life can, sometimes, be affected. The mixing ratio may be e.g. at least 1% or at least 5% (by mass, as indicated above). Thus, in an embodiment, a mass flow ratio of the second throughput 220 to the first throughput 210 is at least 1% or at least 5%, such as from 1% to 100%, or from 2% to 50%, or from 5% to 20%.
The properties of the sealing agent 200 may depend on the mixing ratio. Thus, for improving quality (i.e. reducing variance in products), the mixing ratio is preferably controlled. Referring to
The method may comprise measuring at least one of the mass flow of the first throughput 210 and/or the mass flow of the second throughput 220; and controlling at least one of the first extrusion device 310 and the second extrusion device 320 so as to achieve a target mixing ratio by using the measured value(s) of the mass flow(s). Evidently, the target mixing ratio may be within the limit discussed above.
The sealing agent 200, i.e. a mixture comprising at least the base elastomer and the curing agent, is in use of the pneumatic tire 100 configured to stay attached to the inner surface 102 of the pneumatic tire 100 and to seal punctures of the pneumatic tire 100. In an embodiment, the sealing agent 200 is tacky such that the tackiness enables the sealing agent to stay attached to the inner surface of the pneumatic tire 100 in use and enables sealing of punctures of the pneumatic tire 100 in use.
Preferably, a silicone based sealing agent 200 is used. Thus, in an embodiment, the base elastomer comprises silicone based material or silicone. More preferably the base elastomer comprises silicone. An example of such a material is detailed below.
The use of a two-component sealing agent 200 has the further benefit, that the process can be carried out at room temperature. Thus, as opposed to some prior art solutions, no heater for the sealing agent is needed. Therefore, in an embodiment, a temperature of the sealing agent 200 within the dispensing head 410 is from −10° C. to +50° C. The temperature may be e.g. from +10° C. to +40° C. Moreover, the first throughput 210 and the second throughput 220 may also be substantially at room temperature. Thus, in an embodiment, temperatures of the first throughput 210 and the second throughput 220 are, upstream from the point 212 of mixing, from −10° C. to +50° C. The temperatures may be from +10° C. to +40° C. A temperature of the first throughput 210 may be within either of these ranges throughout from the first extrusion device 310 to the point of mixing 212. A temperature of the second throughput 220 may be within either of these ranges throughout from the second extrusion device 320 to the point of mixing 212. A temperature of the sealing agent 200 may be within either of these ranges throughout from the point of mixing 212 to an outlet 411 of the dispensing head 410.
Referring to
Thus, in an embodiment, before applying the sealing agent 200, the tire 100 has been pre-manufactured, vulcanized and cooled to a storage temperature. Then, the tire 100 is positioned to a tire rotator device 500 such that the rotational axis AX of the tire 100 is more or less horizontal and the tire 100 is rotated around said rotational axis AX. The rotational axis AX may form e.g. an angle of at most 60 degrees with a horizontal direction. The rotational axis AX may be horizontal. The reference numeral 500 is shown in
Preferably, the sealing agent 200 is extruded as an adhesive band 202 or bands 202a, 202b, 202c on to the inner surface 102 by the dispensing head 410. Thus, the dispensing head 410 and/or the tire 100 are moved relative to each other in a direction of the rotational axis AX. The arrow D in
Referring top
Referring top
Referring to
Thus, an embodiment comprises applying the sealing agent 200 to the inner surface 102 of the pneumatic tire 100 in the form of a band 202 or bands 202a, 202b, 202c of which width is less than a half of the width of the pneumatic tire 100. Moreover, the layer of the sealing agent 200 applied on the inner surface 102 of the pneumatic tire 100 comprises the bands 202a, 202b, 202c or parts (202r, 202s, 202t) of the helical band 200 arranged side by side, optionally in an at least partly overlapping fashion.
In order to properly apply the sealing agent 200 onto the inner surface 102 in a reliable manner, preferably, at least an outlet 411 of the dispensing head 410 is arranged inside a space V defined by a carcass 105 of the pneumatic tire 100. Herein the term “space V defined by a carcass 105 of the pneumatic tire 100” refers to such a space that is the smallest convex space encompassing the carcass 105 of the pneumatic tire 100. Moreover, the term “convex space” refers, as conventional, to such a space, wherein any two points within the convex space can be connected by a straight line segment that is encompassed by the convex space. I.e. given any two points of the convex space, the convex space contains the whole line segment that joins the two points. Thus, e.g. cylinder is a convex space, but a hollow cylinder is not. Moreover, e.g. a toroid is not a convex space.
In other words, the space V defined by the carcass 105 is delimited by the tread 110, a first plane P1 that comprises a circular part of the first sidewall 122, and a second plane P2 that comprises a circular part of the second sidewall 124. Moreover, notwithstanding the circular part, the whole first sidewall 122 is arranged on only one side of the first plane P1. Correspondingly, notwithstanding the circular part, the whole second sidewall 124 is arranged on only one side of the second plane P2. Reference is made to
Referring to
However, referring to
To ensure sufficient mixing of the first throughput 210 with the second throughput 220, in an embodiment, the dispensing head 410 comprises a mixer 412. Such a mixer 412 is shown e.g. in
The mixer 412 is configured to mix the material or materials passing through the mixer 412. Thus the mixer 412 is configured to (i) mix the first throughput 210 with the second throughput 220 and/or (ii) mix the sealing agent 200 formed by mixing the first throughput 210 with the second throughput 220. Concerning the latter, referring to
Preferably, at least a part of the mixer 412 is arranged in the space V. This ensures that the sealing agent 200 is being mixed at least nearly until the outlet 411.
As indicated above, the method is applicable to any two component sealing agent or multi component sealing agent. In general, more than two chemicals may be needed to activate the cross-linking process of the sealing agent. As an example, the sealing agent may comprise three components (hereinafter A, B, and C) so that when all the three components A, B, and C are intermixed, the curing (i.e. cross-linking) reaction starts. Thus a first part of the sealing agent (i.e. base elastomer as discussed above) may comprise one or two of A, B, and C, and the other part of the sealing agent (i.e. curing agent as discussed above) may comprise one or two of A, B, and C, so that, in combination, the base elastomer and the curing agent comprise A, B, and C.
The first component (A) may comprise a curable silyl terminated polymer having at least a hydroxyl functional group per molecule. The second component (B) may be or comprise a cross-linker. If the first component comprises the silyl terminated polymer, the cross-linker may be selected from the group of silanes having at least 2 hydrolysable groups; or in the alternative, the cross-linker may be selected from the group of silyl functional molecules having at least 2 silyl groups. Such cross-linkers are capable of cross-linking with the silyl terminated polymer of the component A. However, without a catalyst, the reaction does not occur, or is at least extremely slow. Thus, a suitable catalyst is also needed. In such a case, the component (C) may be a catalyst selected from the group of titanates and/or zirconates. The function of the component (C) is to increase the speed at which the composition (A and B; and C as the catalyst) cures.
Thus, the silyl of the component (A) is cross-linked by the component (B), i.e. the cross-linker, but only in the presence of the reaction catalyst (C). In a preferable embodiment, the base elastomer comprises the components A and B without C. Correspondingly in the embodiment, the curing agent comprises the constituent C, and may comprise only one of A and B. Thus, even if such a material is inherently a three component material, it may be provided as a two component material. However, all the three components may be provided separately. Applying a three component material is detailed in
Each one of the constituents A, B, and C may be extruded by its own extrusion device. Reference is made to
In a preferable embodiment, the base elastomer comprises the components A and B without C; the curing agent comprises the constituent C; and the base elastomer and the curing agent are extruded separately. Reference is made to
In addition, the sealing agent 200 may comprise filler material. Filler material may form a part of the base elastomer or a part of the curing agent. In the alternative, filler material may be separately added upstream from the point of mixing 212 to any one of the throughputs 210, 220 or any one of their parts (210a, 210b, 220a, 220b). The filler material may comprise for example reinforcing and/or non-reinforcing inorganic fillers, thermally and/or electrically conductive fillers e.g. metallic fillers and meltable fillers, or a combination thereof.
Both the base elastomer and the curing agent, before mixed together, have a viscosity that permits the materials to be extruded as discussed above. As an example, in an embodiment, a viscosity of the base elastomer (before mixing) may be at least 40 Pa·s as measured by a Brookfield cone plate viscometer RV DIII using the most appropriate cone plate for the viscosity of the composition and using a shear rate of 1/s at room temperature. However, when cured, the sealing agent has such a viscosity that permits the sealing agent to flow into and seal a puncture in a tire. As an example, in an embodiment, a viscosity of the base elastomer (before mixing) is at most 5000 Pa·s as measured as indicated above (shear rate 1/s and at room temperature), and a viscosity of the curing agent (before mixing) is at most 5000 Pa·s as measured as indicated above. These values ensure sufficiently easy flow of the material during extrusion and mixing. Preferably, in terms of rheology, the base elastomer is non-Newtonian and the behavior is pseudoplastic (sometimes called shear thinning). In other terms, its viscosity depends on the shear rate that is used to determine the viscosity in such a way that the viscosity decreases as the shear rate increases. In general this has the effect that the faster the extrusion of the base elastomer, the easier the extrusion thereof. For example, for a shear rate of 0.01/s, the viscosity may be around 30000 Pa·s at room temperature, and at least materials with a viscosity of less than 100000 Pa·s (shear rate 0.01/s and at room temperature) are also usable. Typically the base elastomer forms a major portion of the sealing agent, whereby this applies to the sealing agent, too.
In an embodiment, the pneumatic tire 100 comprises an innerliner 130. A function of the innerliner 130 is to decrease air permeability. It has been found that the innerliner 130 achieves this aim at least when the innerliner comprises butyl rubber, preferably halobutyl rubber. Bromobutyl rubber and chromobutyl rubber are examples of halobutyl rubbers.
For this technical function it is not so important, which one of the layers of the tire is the innerliner. However, most commonly at least a part of the innerliner 130, or an inside tire paint covering the innerliner 130, forms at least a part of the inner surface 102 of the tire 100. When the innerliner 130 or the inside tire paint forms at least a part of the inner surface 102 (e.g. as in
In case the inner surface 102 (e.g. the innerliner 130 and/or the inside tire paint) has become dirty during storage and/or transportation, the inner surface may be cleaned before applying the sealing agent. Moreover, a conventional one-component sealant typically requires removal of the inside tire paint (if used) before application of the sealant onto the inner surface 102 of the tire. However, it has surprisingly been found that removal of the inside tire paint is not necessary, when a two-component sealing agent 200 comprising silicone is used.
To this end, normally, when a pneumatic tire is manufactured, it is loaded in a curing press to cure the green tire to from the pneumatic tire. Moreover, before the tire is loaded in the curing press, the inside surface of the tire 100, e.g. an inside surface of the innerliner 130, is coated with an inside tire paint. A function of the inside tire paint is to act as a lubricant between the tire innerliner 130 and the curing bladder both during the loading or shaping stage and the stripping stage of the molding operation. Unless adequate lubrication is provided between the bladder and innerliner 130, the bladder tends to stick to the tire. Another function of the inside tire paint is to avoid entrapment of major air bubbles between the tire innerliner and the bladder at the beginning of the shaping operation and to promote entry of air between the bladder and the tire innerliner at the end of the molding operation to avoid adhesion of the tire innerliner to the bladder when the bladder is evacuated prior to withdrawal from within the tire.
An inside tire paint that can be used is a conventional filler-containing, water-based inside tire paint. The inside tire paint may comprise a wax dispersion. The inside tire paint may comprise rubber latex. As a filler material, a mica and/or a silicate may be used. In addition, the inside tire paint may comprise a siloxane or siloxanes, such as polydimethylsiloxane.
In general, micas have the chemical formula X2Y4-6Z8O20(OH, F)4, wherein X is K, Na, or Ca or less commonly Ba, Rb, or Cs; Y is Al, Mg, or Fe or less commonly e.g. Mn, Cr, Ti, or Li; Z is typically Si or Al, but also may include Fe3+ or Ti. Silicates on the other hand are anions consisting of silicone and oxygen.
Therefore, after curing the tire, the inner surface 102 of the pneumatic tire 100 may be formed by a layer of inside tire paint applied onto an innerliner 130. Thus, a layer comprising filler material (e.g. silicate and/or mica) and/or wax may form the inner surface 102 of the tire 100, onto which inner surface 102 the sealing agent 200 may be applied as indicated above.
In an embodiment, the tire comprises an innerliner 130 and the inside tire paint is not cleaned before application of the sealing agent 200. In such an embodiment, a layer of inside tire paint arranged onto the innerliner 130 forms at least a part of the inner surface 102 and at least a part of the sealing agent 200 is applied onto the layer of the inside tire paint. In an embodiment, a layer of inside tire paint that comprises silicate and/or mica is arranged on the innerliner 130 and forms at least a part of the inner surface 102; and at least a part of the sealing agent 200 is applied onto the layer of the inside tire paint. More preferably, in such an embodiment the sealing agent 200 comprises silicone. It has been surprisingly found that the silicone based sealing agent 200 adheres well to the mica or silicate of inside tire paint. In this embodiment, the a layer of inside tire paint that comprises silicate and/or mica further comprises siloxane, such as polydimethylsiloxane.
However, as indicated above, the layer of the inside tire paint may be removed before the application of the sealing agent 200 if considered feasible. In an embodiment, the tire comprises an innerliner 130 and the inside tire paint is removed before application of the sealing agent 200. In such an embodiment, the innerliner 130, which is free from the inside tire paint, forms at least a part of the inner surface 102 and at least a part of the sealing agent 200 is applied onto at least a part of the innerliner 130, which is free from the inside tire paint. Preferable materials for the innerliner 130 have been discussed above.
Number | Date | Country | Kind |
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20215194 | Feb 2021 | FI | national |