Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F224/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
  • C08K5/0025—Crosslinking or vulcanising agents; including accelerators
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
  • C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
  • C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
  • C08G65/002—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds
  • C08G65/005—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens
  • C08G65/007—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens containing fluorine
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/16—Nitrogen-containing compounds
  • C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
  • C08K5/24—Derivatives of hydrazine
  • C08K5/25—Carboxylic acid hydrazides
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
  • C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
  • C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
  • C08L27/18—Homopolymers or copolymers or tetrafluoroethene
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
  • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
  • C08F220/42—Nitriles

Definitions

• This invention relates to curable fluoroelastomer compositions and more particularly to fluoroelastomer compositions containing certain hydrazides as curing agents.
• Fluoroelastomers have achieved outstanding commercial success and are used in a wide variety of applications in which severe
• these polymers are often used in seals for aircraft engines, in oil- well drilling devices, and in sealing elements for industrial equipment that operates at high temperatures.
• fluoroelastomers are largely attributable to the stability and inertness of the copolymerized fluorinated monomer units that make up the major portion of the polymer backbones in these compositions.
• monomers include vinylidene fluoride, hexafluoropropylene, tetrafluoroethylene and peril uoro(alkyl vinyl) ethers.
• fluoroelastomers are typically crosslinked, i.e. vulcanized. To this end, a small percentage of cure site monomer is copolymerized with the fluorinated monomer units.
• Cure site monomers containing at least one nitrile group for example perfluoro-8-cyano-5-methyl-3,6-dioxa-1 -octene, are especially preferred.
• Such compositions are described in U.S. Patents 4,281 ,092; 4,394,489; 5,789,489; 5,789,509 and in WO 201 1084404.
• Bisamidoximes U.S. Patent 5,668,221
• bisamidrazones U.S. Patents 5,605,973; 5,637,648
• cures may be scorchy, i.e. crosslinking may begin before the final shaping of the composition.
• curatives require complex, multistep syntheses from expensive starting materials.
• Fluoropolymers having pendant amidrazone or amidoxime groups are also known (U.S. Patent 7,300,985 B2). These polymers require an additional polymer modification step in order to form crosslinks.
• the present invention is directed to curable fluoroelastomer compositions which comprise a fluoroelastomer having nitrile group cure sites and certain hydrazide as curatives. More specifically, the present invention is directed to a curable composition comprising:
• R 1 is NH 2 , NHNH 2 , NHR 3 , NR 3 2 , NHNHC(O)NH 2 ,
• R 2 is H, alkyl, aryl, heterocycle, CO 2 R 3 , C(O)R 3 , CH 2 R 4 , or C(O)R 4 ;
• R 3 is alkyl, aryl, heterocycle, or CH 2 R 4 ; and
• R 4 is a fluoroalkyl group.
• Another aspect of the present invention is a cured article made from the above composition.
• the fluoroelastomer that may be employed in the composition of the invention may be partially fluorinated or perfluorinated.
• Fluoroelastomers preferably contain between 25 and 70 weight percent, based on the total weight of the fluoroelastomer, of copolymerized units of a first monomer which may be vinylidene fluoride (VF 2 ) or tetrafluoroethylene (TFE).
• the remaining units in the fluoroelastomers are comprised of one or more additional copolymerized monomers, different from said first monomer, selected from the group consisting of
• fluoromonomers hydrocarbon olefins and mixtures thereof.
• Fluoromonomers include fluorine-containing olefins and fluorine-containing vinyl ethers.
• Fluorine-containing olefins which may be employed to make fluoroelastomers include, but are not limited to vinylidene fluoride (VF 2 ), hexafluoropropylene (HFP), tetrafluoroethylene (TFE), 1 ,2,3,3,3- pentafluoropropene (1 -HPFP), 1 ,1 ,3,3,3-pentafluoropropene (2-HPFP), chlorotrifluoroethylene (CTFE) and vinyl fluoride.
• VF 2 vinylidene fluoride
• HFP hexafluoropropylene
• TFE tetrafluoroethylene
• 1 -HPFP 1,2,3,3,3- pentafluoropropene
• 2-HPFP 1,1 ,3,3,3-pentafluoropropene
• CFE chlorotrifluoroethylene
• Fluorine-containing vinyl ethers that may be employed to make fluoroelastomers include, but are not limited to perfluoro(alkyl vinyl) ethers.
• Perfluoro(alkyl vinyl) ethers (PAVE) suitable for use as monomers include those of the formula
• R f , and R f are different linear or branched perfluoroalkylene groups of 2-6 carbon atoms, m and n are independently 0-10, and R f is a perfluoroalkyl group of 1 -6 carbon atoms.
• a preferred class of perfluoro(alkyl vinyl) ethers includes
• X is F or CF3
• n is 0-5
• Rf is a perfluoroalkyl group of 1 -6 carbon atoms.
• a most preferred class of perfluoro(alkyl vinyl) ethers includes those ethers wherein n is 0 or 1 and R f contains 1 -3 carbon atoms.
• Examples of such perfluorinated ethers include peril uoro(methyl vinyl ether) (PMVE), perfluoro(ethyl vinyl ether) (PEVE) and perfluoro(propyl vinyl ether) (PPVE).
• Other useful monomers include those of the formula
• Additional perfluoro(alkyl vinyl) ether monomers include compounds of the formula
• the PAVE content generally ranges from 25 to 75 weight percent, based on the total weight of the fluoroelastomer. If perfluoro(methyl vinyl ether) is used, then the fluoroelastomer preferably contains between 30 and 65 wt.% copolymerized PMVE units.
• Hydrocarbon olefins useful in the fluoroelastomers employed in the invention include, but are not limited to ethylene and propylene. If copolymerized units of a hydrocarbon olefin are present in the fluoroelastomers employed in the invention
• fluoroelastomers hydrocarbon olefin content is generally 4 to 30 weight percent.
• the fluoroelastomer further contains copolymerized units of at least one cure site monomer, generally in amounts of from 0.1 -5 mole percent. The range is preferably between 0.3-1 .5 mole percent. Although more than one type of cure site monomer may be present, most commonly one cure site monomer is used and it contains at least one nitrile substituent group. Suitable cure site monomers include nitrile-containing fluorinated olefins and nitrile-containing fluorinated vinyl ethers. Useful nitrile- containing cure site monomers include those of the formulas shown below.
• n 2-12, preferably 2-6;
• CF 2 CF-O[CF2-CFCF3-O]n-CF2-CFCF 3 -CN (VII)
• n 0-4, preferably 0-2;
• cure site monomers are perfluorinated polyethers having a nitrile group and a trifluorovinyl ether group.
• a most preferred cure site monomer is
• CF 2 CFOCF2CF(CF3)OCF2CF 2 CN
• X perfluoro(8-cyano-5-methyl-3,6-dioxa-1 -octene) or 8-CNVE.
• a first aspect of this invention is a curable composition
• a curable composition comprising A) a fluoroelastomer comprising copolymerized units of a cure site monomer selected from the group consisting of nitrile-containing
• the hydrazide may be a mono-, di-, or poly-hydrazide.
• the hydrazide is of the general formula R 1 (C(O)) n NHNHR 2 , wherein n is 1 or 2; R 1 is NH 2 , NHNH 2 , NHR 3 , NR 3 2 , NHNHC(O)NH 2 , NHNHC(O)NHNH 2 , NHNHR 2 , or NHC(O)NHNH 2 ; R 2 is H, alkyl, aryl, heterocycle, CO 2 R 3 , C(O)R 3 , CH 2 R 4 , or C(O)R 4 ; R 3 is alkyl, aryl, heterocycle, or CH 2 R 4 ; and R 4 is a fluoroalkyi group.
• the alkyl, aryl, benzyl or heterocycle groups may contain additional functional groups such as, but not limited to halogen, ether, or amide groups.
• the fluoroalkyi group has at least one of the hydrogen atoms replaced by fluorine and may optionally contain 1 or more oxygen atoms in the chain.
• R 2 , R 3 , or R 4 may have 1 , 2, or more points of attachment to a hydrazide to afford mono-, di-, or poly-hydrazide.
• hydrazides may also be employed in the composition of the invention.
• the hydrazide may also be a salt, e.g. semicarbazide hydrochloride.
• the oxygen atom may be replaced by sulfur.
• Preferred hydrazides include those wherein n is 1 ; R 1 is NH 2 , NHNH 2 , NHR 3 , NR 3 2, NHNHC(O)NH 2 , NHNHC(O)NHNH 2 , NHNHR 2 , or NHC(O)NHNH 2 ; and R 2 is H; n is 2; R 1 is NH 2 , NHNH 2 , NHR 3 , NR 3 2 , NHNHC(O)NH 2 , NHNHC(O)NHNH 2 , NHNHR 2 , or NHC(O)NHNH 2 ; and R 2 is H; n is 1 ; R 1 is NH 2 , NHNH 2 , NHR 3 , NR 3 2 , NHNHC(O)NH 2 ,
• R 1 is NH 2 , NHNH 2 , NHR 3 , NR 3 2 , NHNHC(O)NH 2 , NHNHC(O)NHNH 2 , NHNHR 2 , or NHC(O)NHNH 2 ; and R 2 is CO 2 R 3 .
• hydrazide curatives include, but are not limited to carbohydrazide; carbonic dihydrazide, dihydrochloride; 4- phenylsemicarbazide; 4-phenylsemicarbazide hydrochloride; 4,4- diphenylsemicarbazide; oxamic hydrazide; oxalyldihydrazide;
• diaminobiuret thiocarbohydrazide
• thiosemicarbazide An example of a dihydrazide is p-phenylenebissemicarbazide. More preferred hydrazides include carbohydrazide; 4-phenylsemicarbazide; oxamic hydrazide;
• these hydrazides act as curing agents by causing the dimerization of polymer chain bound nitrile groups to form 1 ,2,4- triazole rings, thus crosslinking the fluoroelastomer.
• the hydrazides are less volatile than curatives such as hydrazine or t-butyl carbazate, making the hydrazide curatives less likely to be fugitive during mixing and shaping processes.
• the level of hydrazide should be about 0.05 to 7 parts hydrazide per 100 parts fluoroelastomer, preferably about 0.1 to 3 parts hydrazide per 100 parts fluoroelastomer, most preferably about 0.5 to 2 parts hydrazide per 100 parts fluoroelastomer.
• parts refers to parts by weight, unless otherwise indicated.
• An appropriate level of hydrazide can be selected by considering cure properties, for example the time to develop maximum moving die rheometer (MDR) torque and minimum Mooney scorch of the curable compositions.
• MDR moving die rheometer
• the optimum level will depend on the particular
• a curative accelerator e.g. a compound that releases ammonia at curing temperatures
• a hydrazide curative examples include those disclosed in U.S. 6,281 ,296 B1 and U.S. 201 1/0009569.
• curative commonly employed to crosslink fluoroelastomers having nitrile-group cure sites may be used in addition to the hydrazide.
• examples of such other curatives include, but are not limited to diaminobisphenol AF, 2,2-bis(3-amino-4- anilinophenyl)hexafluoropropane, mono- or bis-amidines, mono- or bis- amidrazones, mono- or bis-amidoximes, or an organic peroxide plus coagent.
• Additives such as carbon black, fluoropolymer micropowders, stabilizers, plasticizers, lubricants, fillers, and processing aids typically utilized in fluoroelastomer compounding can be incorporated into the compositions of the present invention, provided they have adequate stability for the intended service conditions.
• the curable compositions of the invention may be prepared by mixing the fluoroelastomer, hydrazide and other components using standard rubber compounding procedures.
• the components may be mixed on a two roll rubber mill, in an internal mixer (e.g. a
• the curable compositions may then be crosslinked (i.e. cured) by application of heat and/or pressure.
• a press cure cycle is generally followed by a post cure cycle during which the press cured composition is heated at elevated temperatures in excess of 300°C for several hours.
• the curable compositions of the present invention are useful in production of gaskets, tubing, and seals.
• Such cured articles are generally produced by molding a compounded formulation of the curable
• the cured compositions have excellent thermal stability, steam and chemical resistance. Volume swell (ASTM D1414) after exposure to 225°C water for at least 168 hours, preferably at least 336 hours, is less than 5%. Also compression set, 300°C, 70 hours, 15% compression (ASTM D395) is less than 70%.
• the cured compositions are particularly useful in applications such as seals and gaskets for manufacturing semiconductor devices, and in seals for high temperature automotive uses.
• fluoropolymers containing nitrile cure sites such as fluoroplastics may be substituted for fluoroelastomers in the compositions of the invention.
• Moving die frequency 1 .66 Hz
• Oscillation amplitude ⁇ 0.5 degrees
• Sample size Disks having diameter of 1 .5 inches (38 mm)
• M H maximum torque level, in units of dN-m
• _ minimunn torque level, in units of dN m
• Tc90 time to 90% of maximum torque, minutes Test specimens were prepared from elastomer compounded with appropriate additives, as described in the formulations listed in the
• Compression set of O-ring samples was determined in accordance with ASTM D395. Mean values are reported.
• volume swell in water was measured at 225°C for the time indicated in the Tables in accordance with ASTM D1414.
• fluoroelastomer polymers were used in the Examples: FFKM - A terpolymer containing 61 .8 mole percent units of TFE, 37.4 mole percent units of PMVE and 0.80 mole percent units of 8-CNVE was prepared according to the general process described in U.S. Patent No. 5,789,489.
• Curable compositions of the invention were compounded on a two- roll rubber mill in the proportions shown in Table I.
• the compounded compositions are labeled Example 1 (4-phenylsemicarbazide, available from Alfa-Aesar) and Example 2 (carbohydrazide, available from Sigma- Aldrich) in Table I.
• Cure characteristics of the compounded compositions are also shown in Table I.
• O-rings were made by press curing the curable compositions at a temperature of 190°C for Tc90 plus 5 minutes, followed by a post cure in a nitrogen atmosphere at a temperature of 305°C for 26 hours after a slow temperature ramp up from room temperature.
• o-rings were made from a similar compound, but containing 0.25 phr urea as curative, rather than a hydrazide curative. After only 168 hours of exposure to 225°C water, the urea cured o-rings exhibited a 15.7 % volume swell.
• Curable compositions of the invention were compounded on a two- roll rubber mill in the proportions shown in Table II.
• the compounded compositions are labeled Example 3 (oxamic hydrazide, available from Acros Organics), Example 4 (oxalyl dihydrazide, available from Sigma- Aldrich) and Example 5 (semicarbazide, prepared from urea and hydrazine hydrate according to the general procedure in Example 1 of U.S. 4,482,738, except hydrogen chloride was omitted) in Table II.
• Cure characteristics of the compounded compositions are also shown in Table II. TABLE II
• Curable compositions of the invention were compounded on a two- roll rubber mill in the proportions shown in Table III.
• the compounded compositions are labeled Example 6 (4-phenylsemicarbazide
• Example 7 (4,4- diphenylsemicarbazide, prepared from diphenylcarbamoyl chloride and anhydrous hydrazine)
• Example 8 (semicarbazide hydrochloride, available from Sigma-Aldrich) in Table III. Cure characteristics of the compounded compositions are also shown in Table III. TABLE III
• a curable composition of the invention was compounded on a two- roll rubber mill in the proportions shown in Table IV.
• the compounded composition is labeled Example 9 (carbohydrazide) in Table IV.
• Cure characteristics (at 199°C) of the compounded compositions are also shown in Table IV.
• O-rings were made by press curing the curable composition at a temperature of 199°C for Tc90 plus 5 minutes, followed by a post cure in a nitrogen atmosphere at a temperature of 260°C for 8 hours after a slow temperature ramp up from room temperature.
• Compression set is also shown in Table IV.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Manufacturing & Machinery (AREA)
• Materials Engineering (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Manufacture Of Macromolecular Shaped Articles (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Priority Applications (3)

Applications Claiming Priority (2)

Publications (1)

Family

ID=46000350

Family Applications (3)

Family Applications Before (2)

Country Status (5)

Families Citing this family (7)

Citations (14)

Family Cites Families (14)

• 2012
  • 2012-03-15 US US13/420,692 patent/US8816013B2/en active Active
  • 2012-03-15 US US13/420,719 patent/US8765876B2/en active Active
  • 2012-03-15 US US13/420,697 patent/US8765875B2/en active Active
  • 2012-03-30 KR KR1020137028200A patent/KR101812371B1/ko active Active
  • 2012-03-30 KR KR1020137028199A patent/KR101769657B1/ko active Active
  • 2012-03-30 EP EP12723766.7A patent/EP2691453B1/en active Active
  • 2012-03-30 WO PCT/US2012/031726 patent/WO2012135785A1/en not_active Ceased
  • 2012-03-30 EP EP12716836.7A patent/EP2691452B1/en active Active
  • 2012-03-30 WO PCT/US2012/031721 patent/WO2012135782A1/en not_active Ceased
  • 2012-03-30 KR KR1020137028205A patent/KR101776986B1/ko active Active
  • 2012-03-30 EP EP12730072.1A patent/EP2691455B1/en active Active
  • 2012-03-30 JP JP2014502887A patent/JP5864719B2/ja active Active
  • 2012-03-30 WO PCT/US2012/031734 patent/WO2012135790A1/en not_active Ceased
  • 2012-03-30 JP JP2014502890A patent/JP5908970B2/ja active Active
  • 2012-03-30 JP JP2014502888A patent/JP5798235B2/ja active Active

Patent Citations (16)

Also Published As

Similar Documents

Legal Events