The invention is related to a viscous polymer composition, a process for producing said viscous polymer composition, a composite comprising said viscous polymer composition, shoe soles comprising said viscous polymer composition or said composite, respectively, as well as the use of the viscous polymer composition or of the composite, respectively, for producing bodies, in particular shoe soles.
By contacting the ground during walking, running or jumping forces are acting between the ground and the foot. The name of said forces are usually ground reaction forces (GRF). It can be determined with suitable measuring devices. The order of magnitude of GRF is usually 1-1,5 times the body weight (BW) of the athlete. During running the forces are 2-3 BW and during jumping forces of 5 and 10 BW were measured. The force-time-pattern shows in each kind of foot ground interaction two different phases. A hitting phase a) in the moment when the foot hits the ground, followed by a push phase b), whereby the athlete pushes himself in a forward and upper direction.
Said two kind of forces have different consequences with respect to the bone- and muscle-system:
Impact-forces do nothing to the forces of the athlete. Impact-forces have been considered to be relevant with respect to chronic and degenerative injures of several sports, in particular when the heel is involved. It is therefore one object, to reduce impact-forces by employing suitable constructions for shoe soles. Systems are intended, which easily deform under force and also disperse the energy.
The amount and the duration of the active forces determine the performance of the athlete, i.e. the running force and the jump heights. This means that a certain niveau of active forces has to be saved, when the athlete intends to run a certain speed. It is therefore intended to support such forces. A shoe sole can influence this, which minimizes the energy dispersion as much an possible and generates the necessary suppression at the same time.
Studies have proved that depending on the sport, running speed, anatomic form of the feet, etc. the relative height of the passive and active maximum to each other can vary. Therefore, depending on each single case the situation depicted in
With regard to the suppression systems in sport industry, the following solutions can be obtained from the state in the art:
From U.S. Pat. No. 5,695,850 a concept is known when a sport shoe is applied with a sole part, which should increase the performance of said shoe. This should be obtained by employing shoe- or sole components, respectively, which “regain” the energies, which occur during running and convert said energies in the push phase from the ground (also in the area of the active maximum in
From DE 87 09 757 a sole unit is known, consisting in a running sole and a intermediate sole, being fixed thereon. The intermediate sole is defined by a relatively small, frame-like circulating strip, which defines a unit, which is closed on its lower end by the running sole. Said unit carries two sole parts. One of those sole parts starts at the front foot area and ends at the beginning of the heel, where the second sole part is located. It is preferred that the first sole part consists in a polymer support inlet which has a relative high elasticity when pressure is applied, in a way that during walking with said shoe a foot bed can result on the sole part, which guarantees a certain comfort. The sole part which is located in the heel area builds a shock absorber and consists in shock absorbent, viscous material like silicone.
In a similar way U.S. Pat. No. 4,910,886 describes the use of shock absorbing inlets made of viscous material in the heel area of a sole unit.
U.S. Pat. No. 4,316,335 discloses the use of a viscous shock absorbing material in the front part of a sole as well as in the heel part, wherein the shock absorbing properties in the heel part should be better.
Furthermore, in U.S. Pat. No. 4,418,483 a shoe sole is disclosed, wherein in a layer composition the viscous material which is a polymer composition is implied as one possible layer. Said polymer composition consists in a cross-linked ethylene-vinylacetate copolymer (referred as EVA) and for increasing the tensile strength and other material properties, for example styrene-butadiene-rubber. Furthermore, in said polymer composition silica gel is implied as a filler and furthermore the usual aids for cross-linked rubber are used.
The above described known concepts have the drawback in common that the viscous material suggested therein are not adapted or optimized, respectively, or the above discussed time behavior of the passive and active force maximum in the heel area. For this reason, the desired effect is only unsatisfyingly accomplished and a “fuzzy” or “bouncing” feeling results during running. This causes a significant drawback in efficiency and safety of the forward movement of the runner who uses the shoe.
The object of the present invention is to provide a viscous material, in particular suitable for the passive and active force maximum occurring during the natural movement and which optimally uses a natural movement dynamic and thus provides a safe and efficient forward movement of the runner.
Moreover, it is desired that the viscous material can be used without bigger adaptations in known plants for producing shoe soles in a efficient and cheap manner.
According to the present invention the above objects are solved by a viscous polymer composition, which comprises and in particular contains:
Furthermore, the polymer composition according to the invention can contain the usual aids and additional compounds as for example to simplify removing the polymer composition from a mould.
All possible combinations of the component A with the components B-E are preferred according to the present invention. Furthermore, the component B can be combined with the components C to E. In particular preferred combinations of the components are given by the following letter combinations: AB, AC, AD, AE, AEC, ABCD, BC, ABC, ABCDEF and ABCDE.
Furthermore, the viscous polymer composition is preferred, which contains components:
The amount of component F if present is up to 15 wt-%, preferred from 0.5 to 5 wt-% in relation to the remaining polymer composition.
According to the present invention preferably C4-C8- and in particular preferred C4-C6- and moreover preferred C4-C5-dienes are employed as monomer A1. C4-C5-dienes are preferably butadiene and isoprene, wherein butadiene is in particular preferred.
Particularly C8-C15- and particularly preferred C8-C10-monomers are employed as monomer A2. α-methylstyrene and styrene are preferred and styrene is in particular preferred.
Polymer A is preferably a block polymer, which comprises at least one block of monomer A1 and one block of monomer A2. In particular preferred is a three block copolymer with on block of monomer A2 followed from one block of monomer A1 again followed by one block of monomer A2. A poly-(styrene-butadiene-styrene)-block copolymer as for example available under the trade name Styroflex® by BASF AG is in particular preferred.
Such poly-(styrene-butadiene-styrene)-blockcopolymers consist of “islands” of polystyrene as a hard fiber which are bedded in a matrix of rubber-like statistical styrene-butadiene-copolymer which makes the material flexible. Typically, these materials have a shore A-hardness (3s)15s, according to DIN 53505 in a range of (85 to 90) or 80 to 85 respectively. The shore D-hardness (3s)15s, measured according to DIN 53505, is in a range of (30 to 35) or 27 to 32 respectively. Furthermore, such materials have a low glass transition temperature in the range around −40° C. and a breaking temperature (according to DIN 53372) in a range of approximately −35° C. Further information about this material is given in the data sheets concerning Styroflex®, obtainable from BASF AG, Ludwigshafen.
Polymer B is a copolymer at least formed from the monomers B1 and B2.
The monomer B1 is preferably a C2- to C20- more preferably a C2- to C15- and in particular preferable C2- to C10-olefin. It is moreover preferred that monomer B1 is an alpha-olefin. In particular ethylene, propylene, 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene and 1-nonene are preferred and ethylene as in particular preferred.
Monomer B2, being further employed in polymer B, is the product that is for example obtainable from a vinyl alcohol, in particular with 2 to 8 and more particular with 2 to 5 and even more particular with 2 carbons and a carboxylic acid with particular 2 to 8 and more particular 2 to 5 and even more particular 2 carbon atoms.
Polymer B can contain polymer B2 in a range from 5 to 25 and particular from 15 to 23 wt-%.
Particular preferred as polymer B is EVA(ethylene-vinylacetate)-polymer with a vinyl acetate content of 18 to 21 wt-%, based on the total polymer B in the viscous polymer composition according to the present invention. This EVA-polymer is supplied for example by Leuna Polymer GmbH, DuPont or Exxon.
Within this group of polymers, the content of vinylacetate as well as the melting index of the copolymerisation determine amongst others the mechanical and thermal properties of the polymer. With increasing content of vinylacetate, elongation, tension-tear stability, flexibility, cold resistance, rebound elasticity, tolerance and stickyness increase whereas hardness, stiffness, elasticity, vica temperature, bending stress and resistance towards chemicals decrease.
Further details concerning the properties and the composition of commercially available polymers B, especially of EVA polymers can be obtained from the corresponding data sheet of the above mentioned companies, like for example the data sheets regarding the product Miravithen® of Fa. Leuna Polymer GmbH and Elvax® of DuPont.
Polymer C is a polymer, obtainable from at least one vinylaromatic monomer, like for example styrene. Generally, such polymers are liquid in a temperature range from −10 to 100° C. Preferably, polymer C is liquid in a range from 0 to 70° C., especially preferred from 10 to 50° C. Regarding a C4 to C10-diene, reference is made to the explanation concerning monomer A1.
The halogens in polymer D are preferably fluorine, chlorine and bromine and in particular preferred bromine. With regard to the conjugated dienes employed in polymer D reference is made to monomer B 1. In polymer D bromo butadiene, bromo ispoprene are preferred and bromo butadiene is in particular preferred. Accordingly, poly bromo butadiene rubber is in particular preferred as polymer D.
As examples for materials which can be used as a polymer D, brominated copolymers of isobutene and isoprene have to be mentioned, which are availabel for example under the name Polysar® of Fa. Bayer AG. Further details regarding such polymers which can be used as polymer D are provided in the corresponding data sheet of Fa. Bayer AG.
As filler E all fillers know by the person skilled in the art can be used. Generally, fillers can be divided in inorganic and organic fillers. According to the present invention inorganic fillers are preferred. Said fillers particularly base on Si wherein silicon oxide are more preferred and silica is mostly preferred. Besides increasing the stability the use of fillers also increases the abrasion resistance of the viscous polymer composition.
Further fillers to be mentioned are for example: soot, calcium and aluminium silicates, aluminium oxide, kaolin, silica, french chalk, chalk and metal oxides, like for example zinc oxide and metal carbonates.
Above this, all known inorganic and organic pigments can be used as fillers, wherein pigments of titan oxide, zinc sulfide, iron oxide, chromium oxide, cadmium and chromate are preferred as inorganic pigments, and as organic pigments are especially preferred: diarylic- and pyrazolon-diazopigments, pigments of the β-naphtholcarboxylic acid or β-naphtholcarboxylic acid-arylits, derivatives of naphthalenetetracarboxylic acid or derivatives of peryleneteracarboxylic acid, pigments of dioxazine as well as pigments of chinacridon condensation products, thioindigo-isoindolinone condensation products and diazo condensation products.
Component F are aids and additional compounds which are well-known to the person skilled in the art. Aids are in particular activators, inhibitors, plasticizers, cross-linkers, separating agents, softeners and blowing agents in the case that the viscous polymer composition is a foam.
Activators can be inorganic or organic compounds. According to the present invention it is preferred that the viscous polymer composition contains a organic and an inorganic activator. Fatty acids are preferred organic activators, wherein sterenic acid is in particular preferred. Inorganic activators are in particular oxides of transition metals, wherein zinc oxide is in particular preferred.
Furthermore, it is preferred to add separating agents to the viscous polymer composition. The separating agents known to the person skilled in the art can be employed. In particular suitable are separating agents which are a salt of a fatty acid and a transition metal, wherein zinc stearate is in particular preferred.
Additionally, it is preferred to include softeners in the viscous polymer composition according to the present invention. Suitable softeners are known by the skilled person. Phthalates, adapenic acid ester and polyesters with rather low degree of polymerization are preferred. From these phthalates are in particular preferred, wherein di-octyl phthalate is in particular preferred in the viscous polymer composition according to the present invention.
If it is desired to obtain the viscous polymer composition as a foam, blowing agents can be used which are known to the person skilled in the art. Preferred blowing agents are halogen free carboxylic amides as for example the product ADC/K from Fa. Bayer AG or AC3000H.
The viscous polymer composition according to the present invention can be produced by a process, wherein the above mentioned components are brought into contact. Injection moulding is a preferred method for processing the polymer composition.
Furthermore, the viscous polymer composition according to the present invention is obtainable by bringing the above defined components into contact.
The viscous polymer composition according to the present invention comprises at least one of the following material properties:
An energy loss in the range of 50 to 80, preferably from 55 to 75 and more preferably from 60 to 70%,
The polymer composition according to the present invention can have all possible combinations of the single properties a) to e). Preferred property combinations of the viscous polymer composition according to the present invention are given in the following letter combinations: ab, abc, abcd, abcde, bc, de, ac, ad, ae, ace, be, bd, and ce. In particular preferred is a viscous polymer composition with all properties a) to e).
Furthermore, the invention is related to a composite, comprising or preferably consisting in a viscous polymer composition according to the present invention and an elastic material.
The elastic material of the composite has at least one of the following properties:
Preferably the elastic material of the composite can have the above defined properties a) to E) in all possible combinations. The following combinations are more preferred: αβ, αβχ, αβχδ, αβχδε, αχ, αχ, αε, βχ, βε, βχδ, βχβχδε, χε, χδε, δε. An elastic material in the composite with all the properties α) to ε) is most preferred.
In a preferred embodiment of the composite of the present invention the viscous polymer composition V1 and the elastic material V2 are directly adjacent to each other. This is in particular preferred when the composite only consists in the viscous polymer composition according to the present invention and the elastic material.
In another embodiment of the composite of the present invention the viscous polymer composition V1 and the elastic material V2 are separated at least in one part by at least one further material V3. Said composite preferably consists in the viscous polymer composition V1, the elastic material V2 and a further material V3. The elastic material V2 can be made of all suitable materials, in particular elastic polymers, known by the skilled person. The further material V3 differs from the viscous polymer composition V1 and the elastic material V2 in at least one material property, wherein the further material V3 preferably also differs with respect to its composition from the viscous polymer composition V1 and the elastic material V2.
Furthermore, the invention is related to a body, in particular a shoe sole, inlays for shoes, protectors, especially for elbow and shin, and shoulderpads, comprising, preferably consisting a viscous polymer composition or a composite according to the present invention.
Furthermore, the invention is rated to the use of a viscous polymer composition or a composite according to the present invention for producing of bodies, in particular shoe soles.
Above this, the viscous polymer composition according to the invention can be used to produce bodies in the whole area of healthcare and medical applications like for example health-shoes, orthopaedic shoes, orthopaedic inlays or elbowpads.
The term body generally means forms, foils, fibers, films and coatings. Bodies are preferred in which the properties of the viscous polymer composition or the composite according to the invention or both are favorably applicable.
Preferred embodiments of the present invention are well described under reference of the following drawings, wherein it shows:
a A force-time-diagram of two force fields, which are applied from a measuring device according to the present invention on the heel area and the front foot area of a sole unit according to the present invention or material layers, respectively, to determined the energy loss according to the present invention and the dynamic stiffness;
b a measuring device according to the present invention used for applying the force profile according to
c The force stamps used in a device according to
a a cross-sectional view of an embodiment of the composite according to the present invention or a cut along the line A-A (or B-B, respectively), of the preferred embodiment shown in
b a cross-sectional view of an embodiment of the composite according to the present invention or a cut following the line A-A (or B-B, respectively), of the embodiment of
The preferred embodiments of the present invention are now described by the drawings which are not limiting the scope of the invention.
To describe the principles according to the present invention, with regard to
As shown in
If for proving the above consideration a test person proceeds the movement typical for running on a force-time-measuring platform, the force profile according to
As shown in
After the passive phase of moving the so-called active phase follows in the GRF-diagram. The second force increase in the active phase results from the push of the foot from the ground (reference is made to
Since the force increase of the passive phase occurs much faster as in the active phase, this results in a higher load of the heel, since the applied impulse (stroke) is comparably higher. Furthermore, by hitting a hard surface the impulse is “reflected” from the ground, so that the anatomy has to absorb said impulse. This yields, in particular during long lasting loads (example given marathon runs) to significant injuries or wear out, respectively.
Because of the smaller force impulse (longer force build up time) the load of the front foot area is lower. Furthermore, said front foot area has a bigger surface and an anatomic form, which allows a better absorption.
From his fact it was derived that the heel area needs better protection compared to the front foot area to avoid atomic damages. Since the forces in the front foot area occur slower, the foot is more capable to adapt to the increase of load (which is less here).
It is favorable for the front foot area that the sole has the property, wherein the component of the moving energy directing in the running direction is released as schematical energy in running direction and/or from the ground. Again, reference is made to
The present invention is thus based on the result that in the heel area and in the front foot area of a sole unit materials with different properties should be used: In the front foot area it is preferred to use an elastic material. In contrast to this, it is preferred to use a material obtained from the viscous polymer composition according to the present invention in the heel area.
From the above consideration it becomes apparent that the polymer characterization and the of the viscous polymer composition and the elastic material the energy loss occurring deformation is in particular suitable. This property (measured in %) describes the ratio of the energy applied to the material over the occurring force field to the energy obtained by relaxation.
To determine the energy loss of suitable materials in the present invention the device according to
The force field being implied by the stamp device 7 or stamp 8, respectively, has different profiles in the present invention for the test of the elastic and viscous materials to simulate reality as much as possible. Accordingly, for the testing of suitable viscous polymer a force field is applied, which is called “heel” in
Below, with reference to
The diagram from
Dynamic stiffness DS1000-1500=(F1500N−F1000N)/(d1500N−d1000N)[N/mm]
The value of dynamic stiffness between 200 N and 400 N can be also calculated according to the above equation. Said value is not shown graphically in
The dynamic stiffness is according to the present invention of interest of a sole unit which is a layer assemble (i.e. a plurality of layers from different materials). This of course is one preferred embodiment of the composite according to the present invention. Said assemblies (for example given with an inner layer, a middle layer which can comprise a function layer and an outer sole) show the above described effect according to the present invention only if the stiffness of the function layer is not higher than the stiffness of the materials of which the layers are made.
It becomes apparent that for field sports (basketball, volleyball, soccer) the dynamic stiffness between 1000 N and 1500 N should be lower as 600 N/mm for the elastic material and less than 250 N/mm for the viscous polymer composition.
However, for running shoes the dynamic stiffness of the elastic material between 1000 N and 1500 N should be less than 450 N/mm and the dynamic stiffness for the viscous polymer composition should be less than 200 N/mm.
For a shoe for universal application a good compromise is: The dynamic stiffness of the elastic materials between 1000 N and 1500 N should be less than 600 N/mm and between 200 N and 400 N less than 300 N/mm. The dynamical stiffness of the viscous polymer composition between 1000 N and 1500 N should be less than 250 N/mm and between 200N and 400N less than 130 N/mm.
Taking the above materials into account,
In a preferred embodiment according to the present invention there is between the outer sole 55 and the middle sole 59a function layer 57. Said function layer 57 can be divided in two horizontal areas, i.e. the front foot area 60 with elastic material and the heel area 80 with the viscous polymer composition. Between said two horizontal areas there can be a transition area 70. The front foot area 60 and the heel area 80 can also be in contact.
According to an alternative embodiment of the present invention (not shown) also two functional layers 57 can be present. In such a case the first function layer in the front foot area comprises the elastic material and the second function layer in the heel layer comprises the viscous polymer composition.
As shown in
Number | Date | Country | Kind |
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100 10 182.8 | Mar 2000 | DE | national |
Filing Document | Filing Date | Country | Kind |
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PCT/EP01/02403 | 3/2/2001 | WO |