Compound For Lateral Inserts Of Run-Flat Pneumatic Tires

Abstract

A compound of a lateral insert of a run-flat pneumatic tyre comprising a cross-linkable unsaturated chain polymer base that is capable of assuming all of the chemical-physical and mechanical characteristics of an elastomer after cross-linking, a filler, a plasticizing agent and a curing system. The plasticizing agent consists of an aliphatic chain and has a melting temperature of between 50 C. and 100 C.

Claims

1. Compound of a lateral insert of a run-flat pneumatic tyre comprising a cross-linkable unsaturated chain polymer base that is capable of assuming all of the chemical-physical and mechanical characteristics of an elastomer after cross-linking, a filler, a plasticizing agent and a curing system; said compound being characterized in that said plasticizing agent consists of an aliphatic chain and has a melting temperature of between 50 C. and 100 C.

2. Compound according to claim 1, characterized in that said plasticizing agent has a melting temperature of between 69 C. and 90 C.

3. Compound according to claim 1, characterized in that said aliphatic chain has a length of between C30 and C50.

4. Compound according to claim 1, characterized in that said plasticizing agent is present in compound form in an amount of between 10 and 30 phr.

5. Lateral insert for run-flat pneumatic tyres obtained with a compound according to claim 1.

6. Run-flat pneumatic tyre comprising a lateral insert according to claim 5.

Description

EXAMPLES

[0016] Three comparative compounds were prepared (Compounds A-C) and a compound according to the teachings of the present invention (Compound D).

[0017] In particular, Compound A is free of plasticizing agent; Compound B differs from Compound A by the fact that, with the aim of lowering the hysteresis, it has a lower quantity of carbon black; Compound C differs from Compound A by the fact that it comprises a plasticizing agent characterized by a melting temperature that is lower than that provided according to the present invention, and Compound D differs from Compound A by the fact that it comprises a plasticizing agent with a melting temperature that is in line with that provided according to the present invention.

[0018] The compounds described in the examples were obtained according to the procedure reported below:

[0019] -Preparation of the Compounds-

[0020] (1st Mixing Step)

[0021] Before the start of the mixing, a mixer with tangential rotors and an internal volume of between 230 and 270 liters was loaded with the cross-linkable polymer base, the carbon black, the phenolic acid and, when provided, the plasticizing agent, thus reaching a fill factor of 66-72%.

[0022] The mixer was operated at a speed of 40-60 revolutions/minute, and the mixture thus formed was discharged once a temperature of 140-160 C. had been reached.

[0023] (2nd Mixing Step)

[0024] The mixture obtained from the previous step was re-processed in a mixer that was operated at a speed of 40-60 revolutions/minute and, thereafter, discharged once a temperature of 130-150 C. had been reached.

[0025] (3rd Mixing Step)

[0026] The vulcanization system (Sulfur, accelerants, antioxidants/antiozonants, Zinc Oxide and stearic acid) was added to the mixture obtained from the previous step, reaching a fill factor of 63-67%.

[0027] The mixer was operated at a speed of 20-40 revolutions/minute, and the mixture thus formed was discharged once a temperature of 100-110 C. had been reached.

[0028] Table I lists the compositions in phr of the six compounds.

TABLE-US-00001 TABLE I A B C D S-SBR 70 70 70 70 BR 30 30 30 30 Carbon black 45 30 45 45 Plasticizing agent* 20 Plasticizing agent** 20 Phenolic resin 2.24 2.24 2.24 2.24 Sulfur 6.86 6.86 6.86 6.86 Zinc oxide 5 5 5 5 Stearic acid 1 1 1 1 TMQ 0.7 0.7 0.7 0.7 CBS 4.2 4.2 4.2 4.2 MBTS 1.1 1.1 1.1 1.1 Reinforcing resin 3.5 3.5 3.5 3.5 6PPD 2 2 2 2 S-SBR is a polymer base obtained through a solution polymerization process with an average molecular weight, respectively, of 800-1500x10.sup.3 and of 500-900x10.sup.3, with a styrene content of between 20 and 45%. BR is a butadiene rubber with a 1,4-cis content of at least 40%. The plasticizing agent* is pentadecanoic acid methyl ester characterized by a melting temperature of about 20 C. (less than that provided according to the present invention) The plasticizing agent** is a saturated paraffin with a C40 chain characterized by a melting temperature of 70 C. (in line with that provided according to the present invention). TMQ is the acronym for poly(1,2-dihydro-2,2,4-trimethylquinoline) and is used as an antioxidant. CBS is the acronym for benzothiazyl-cyclohexyl-sulfenamide and is used as a vulcanization accelerant. The reinforcing resin is a phenol-formaldehyde type resin. 6PPD is the acronym for N-1,3-dimethylbutyl-N'-phenyl-paraphenylenediamine and is used as an antioxidant agent.

[0029] The compounds described above were tested in order to evaluate the stiffness and hysteresis characteristics thereof. As is known to a person skilled in the art, the measurement of the elastic modulus E(30 C.) provides an assessment of the stiffness, while the measurement of tan (200 C.) provides an assessment of hysteresis. The elastic modulus E (30 C.) and tan (200 C.) values were obtained according to the ISO 4664 standard.

[0030] Table II lists the stiffness and hysteresis results indexed against the comparative Compound A. In particular, the higher values are those relating to a higher stiffness and a lower hysteresis.

TABLE-US-00002 TABLE II A B C D Stiffness 100 90 95 100 Hysteresis 100 110 105 120

[0031] From the values listed in Table II, it is clear how a decrease in the quantity of carbon black (Compound B) or the use of a plasticizing agent, characterized by a melting point that is different than that provided by the present invention (Compound C), even if this leads to the desired decrease in hysteresis, nonetheless results in an undesired decrease in stiffness.

[0032] In contrast, the use of a plasticizing agent characterized by a melting temperature within the range according to the present invention (Compound D) is capable of ensuring a reduction in the hysteresis value, without this being reflected in a lowering of the stiffness levels.