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WO1999065983A1 - Rubber composition for power transmission belts - Google Patents

Rubber composition for power transmission belts Download PDF

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Publication number
WO1999065983A1
WO1999065983A1 PCT/US1998/011854 US9811854W WO9965983A1 WO 1999065983 A1 WO1999065983 A1 WO 1999065983A1 US 9811854 W US9811854 W US 9811854W WO 9965983 A1 WO9965983 A1 WO 9965983A1
Authority
WO
WIPO (PCT)
Prior art keywords
phr
rubber composition
power transmission
acsm
transmission belts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US1998/011854
Other languages
French (fr)
Inventor
Paul Norman Brinkman
Thomas George Burrowes
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Goodyear Tire and Rubber Co
Original Assignee
Goodyear Tire and Rubber Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Goodyear Tire and Rubber Co filed Critical Goodyear Tire and Rubber Co
Priority to AU79562/98A priority Critical patent/AU7956298A/en
Priority to US09/700,104 priority patent/US6669591B1/en
Priority to PCT/US1998/011854 priority patent/WO1999065983A1/en
Priority to BR9815901-1A priority patent/BR9815901A/en
Priority to JP2000554797A priority patent/JP2002518535A/en
Priority to EP98930092A priority patent/EP1095104A1/en
Priority to ZA9903855A priority patent/ZA993855B/en
Publication of WO1999065983A1 publication Critical patent/WO1999065983A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/26Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
    • C08L23/32Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with compounds containing phosphorus or sulfur
    • C08L23/34Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with compounds containing phosphorus or sulfur by chlorosulfonation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • C08L23/0846Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen
    • C08L23/0853Ethene vinyl acetate copolymers

Definitions

  • HNBR hydrogenated nitrile butadiene rubber
  • ACM alkylated chlorosulfonated polyethylene
  • a rubber composition comprising:
  • a power transmission belt produced from a rubber composition comprising:
  • ACSM used in the present invention
  • EVM is available from Bayer as LEVAPREN 500HV.
  • Typical of the peroxide cure co-agents are trimethylolpropane trimethacrylate, trifunctional organosiloxanes, triallyl cyanurate and triallyl isocyanurate, 1,3-butylene glycol dimethacrylate, ethylene glycol dimethacrylate, and n, n' -m-phenylene-dimaleimide-1, 2-cis- polybutadiene. While from 0.5 to 10 phr of the co-agent can be used, 1 to 4 phr are preferred.
  • Typical of the organic peroxides which can be used with invention are 1, 3-bis (t-butylperoxy-1-propyl) benzene, dicumyl peroxide, ⁇ , ⁇ -bis (t-butylperoxy) valerate, ⁇ , ⁇ -bis(t- butylperoxy) diisopropyl benzene, 2, 5-dimethyll-2, 5-di (t- butylperoxy) hexane, 1, 1-bis (t-butylperoxy) -3, 3, 5- trimethylcyclohexane, n-butyl-4, 4-bis (t-butylperoxy) valerate, and ethyl-3, 3-bis (t-butylperoxy) butyrate..
  • a series of blends of ACSM/EVM were compared to an all ACSM compound, an all EVM compound and three compounds known to be used in positive drive belts comprising a sulfur cured HNBR, a peroxide cured HNBR and a Neoprene for: a) percent of torque S' at 38°C which is retained at 135°C; b) oil resistance as percent volume swell after aging seventy hours at 100°C in IRM 903 oil; and c) the change in 10% modulus of each compound after being in oven for 168 hours @ 135°C.
  • the results are shown in Tables 3, 4 and 5 respectively.
  • modulus retention results further show an unexpected synergistic effect between the ACSM and EVM, such that the %S' retained for certain blend ratios is higher than for ACSM or EVM alone.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

This invention relates to power transmission belts and to a rubber composition for use therein. The composition contains from 90 to 10 phr alkylated chlorosulfonated polyethylene and 10 to 90 phr ethylene vinyl acetate.

Description

RUBBER COMPOSITION FOR POWER TRANSMISSION BELTS Technical Field This invention relates to power transmission belts and to a rubber composition for use therein. Background Art
Continually increasing temperatures in the engine compartment of motor vehicles has resulted in conventional compounds such as neoprene becoming obsolete due to insufficient heat resistance. In many instances, a change has been made to hydrogenated nitrile butadiene rubber (HNBR) . However, HNBR is a very expensive rubber. See e.g. U.S. Patent No. 5,599,246. More recently, the use of alkylated chlorosulfonated polyethylene (ACSM) has been suggested as a lower cost alternative to HNBR. See e.g. U.S. Patent No. 5,711,734; 5,408,007 and 5,626,953. While the ACSM polymer suffer some deficiencies, such as retention of properties at elevated temperatures and oil resistance, when used by itself, we have found that blending the ACSM with ethylene vinyl acetate (EVM) and curing the blends with an organic peroxide and a cure co- agent overcome those deficiencies. Summary of the Invention
In accordance with the practice of the present invention, there is provided a rubber composition comprising:
a. from 90 to 10 parts by weight per 100 parts of rubber (phr) of ACSM; b. from 10 to 90 phr of EVM; c. from 20 to 75 phr of carbon black; and d. from 2 to 10 phr of an organic peroxide.
There is also disclosed a power transmission belt produced from a rubber composition comprising:
a. from 90 to 10 phr of ACSM; and b. from 10 to 90 phr of EVM. The ACSM used in the present invention is available from DuPont-Dow as ACSIUM HPR 6367.. The EVM is available from Bayer as LEVAPREN 500HV.
Typical of the peroxide cure co-agents are trimethylolpropane trimethacrylate, trifunctional organosiloxanes, triallyl cyanurate and triallyl isocyanurate, 1,3-butylene glycol dimethacrylate, ethylene glycol dimethacrylate, and n, n' -m-phenylene-dimaleimide-1, 2-cis- polybutadiene. While from 0.5 to 10 phr of the co-agent can be used, 1 to 4 phr are preferred.
Typical of the organic peroxides which can be used with invention are 1, 3-bis (t-butylperoxy-1-propyl) benzene, dicumyl peroxide, α,α-bis (t-butylperoxy) valerate, α,α-bis(t- butylperoxy) diisopropyl benzene, 2, 5-dimethyll-2, 5-di (t- butylperoxy) hexane, 1, 1-bis (t-butylperoxy) -3, 3, 5- trimethylcyclohexane, n-butyl-4, 4-bis (t-butylperoxy) valerate, and ethyl-3, 3-bis (t-butylperoxy) butyrate.. While 0.5 to 10 phr of the peroxide can be used, 1.5 to 4.5 phr are preferred. While 20 to 75 phr of carbon black can be used, we prefer a mixture of from 15 to 45 phr of a N550 carbon black from Cabot and from 5 to 30 phr of an SRF/N762 carbon black available from Cabot.
Experimental
Figure imgf000005_0001
1. ACSIUM HPR 6367.
2. LEVAPREN 500HV. 3. Poly-Dispersion VC-60, Rhein Chemie.
4. PLASTOMAG 170, Akrochem
5. PE 200, Hercules
Original physicals, compression modulus, oven-aged physicals and oil immersion physicals were run on the blends and are shown in Table 2.
Figure imgf000006_0001
As the data indicate, the blends of ACSM/EVM exhibit better retention of modulus at elevated temperatures and improved resistance to oil.
A series of blends of ACSM/EVM were compared to an all ACSM compound, an all EVM compound and three compounds known to be used in positive drive belts comprising a sulfur cured HNBR, a peroxide cured HNBR and a Neoprene for: a) percent of torque S' at 38°C which is retained at 135°C; b) oil resistance as percent volume swell after aging seventy hours at 100°C in IRM 903 oil; and c) the change in 10% modulus of each compound after being in oven for 168 hours @ 135°C. The results are shown in Tables 3, 4 and 5 respectively.
As the data indicate, significant improvement in retention of modulus at elevated temperatures and oil resistance versus ACSM can be achieved via an ACSM/EVM blend. The modulus retention results further show an unexpected synergistic effect between the ACSM and EVM, such that the %S' retained for certain blend ratios is higher than for ACSM or EVM alone.
Figure imgf000008_0001
Figure imgf000009_0001
Figure imgf000010_0001
While certain representative embodiments and details have been shown for the purpose of illustrating the invention, it will be apparent to those skilled in this art that various changes and modifications may be made therein without departing from the spirit or scope of the invention.

Claims

1. A rubber composition comprising parts by weight per 100 parts of rubber (phr) :
a. from 90 to 10 phr of an alkylated chlorosulfonated polyethylene; b. from 10 phr to 90 phr of an ethylene vinyl acetate copolymer; c. from 20 phr to 75 phr of carbon black; and d. from 2 phr to 10 phr of an organic peroxide.
2. A power transmission belt produced from a rubber composition comprising parts by weight per 100 parts or rubber (phr) ;
a. from 90-10 phr of an alkylated chlorosulfonated polyethylene; and b. from 10-90 phr of an ethylene vinyl acetate copolymer.
3. The rubber composition of claim 1 further comprising from .5 to 10 phr of a peroxide cure co-agent.
4. The belt according to claim 2 further comprising from 20-75 phr of carbon black and from 2-10 phr of an organic peroxide.
5. The belt according to claim 4 further comprising from 0.5 to 10 phr of a peroxide cure co-agent.
PCT/US1998/011854 1998-06-19 1998-06-19 Rubber composition for power transmission belts Ceased WO1999065983A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
AU79562/98A AU7956298A (en) 1998-06-19 1998-06-19 Rubber composition for power transmission belts
US09/700,104 US6669591B1 (en) 1998-06-19 1998-06-19 Rubber composition for power transmission belts
PCT/US1998/011854 WO1999065983A1 (en) 1998-06-19 1998-06-19 Rubber composition for power transmission belts
BR9815901-1A BR9815901A (en) 1998-06-19 1998-06-19 Rubber composition for force transmitting belts
JP2000554797A JP2002518535A (en) 1998-06-19 1998-06-19 Rubber composition for power transmission belt
EP98930092A EP1095104A1 (en) 1998-06-19 1998-06-19 Rubber composition for power transmission belts
ZA9903855A ZA993855B (en) 1998-06-19 1999-06-08 Rubber composition for power transmission belts.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US1998/011854 WO1999065983A1 (en) 1998-06-19 1998-06-19 Rubber composition for power transmission belts

Publications (1)

Publication Number Publication Date
WO1999065983A1 true WO1999065983A1 (en) 1999-12-23

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PCT/US1998/011854 Ceased WO1999065983A1 (en) 1998-06-19 1998-06-19 Rubber composition for power transmission belts

Country Status (5)

Country Link
EP (1) EP1095104A1 (en)
JP (1) JP2002518535A (en)
AU (1) AU7956298A (en)
WO (1) WO1999065983A1 (en)
ZA (1) ZA993855B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2910615A4 (en) * 2012-10-17 2016-06-22 Bridgestone Corp CURED SHEET, LAMINATE BODY USING THE SAME, AND PROCESS FOR PRODUCING THE LAMINATED BODY

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4180531A (en) * 1976-11-16 1979-12-25 Dominic Alia Processible and vulcanizable polar polymers
US5322479A (en) * 1991-12-26 1994-06-21 Caoutchouc Manufacture Et Plastiques Endless belt power transmission system

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4180531A (en) * 1976-11-16 1979-12-25 Dominic Alia Processible and vulcanizable polar polymers
US4180531B1 (en) * 1976-11-16 1987-03-10
US5322479A (en) * 1991-12-26 1994-06-21 Caoutchouc Manufacture Et Plastiques Endless belt power transmission system

Also Published As

Publication number Publication date
JP2002518535A (en) 2002-06-25
ZA993855B (en) 1999-12-08
AU7956298A (en) 2000-01-05
EP1095104A1 (en) 2001-05-02

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