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    METHODS FOR THE BINDING OF POLYMER COMPOSITIONS IN THE PRESENCE OF ATMOSPHERIC OXYGEN A process for the crosslinking of an elastomer composition in the presence of an organic peroxide formulation is disclosed. The formulation of organic peroxides can comprise additional compounds chosen from superior bis, tri and polyimaleides, bis, tri and superior polytraconimides, peroxide-crosslinkable silicone elastomers, p-phenylenediamine-based antiozonants, sulfur-containing organic compounds that are accelerators for curing with sulfur (crosslinking) of curable / crosslinkable polymers with sulfur, and polysulfide polymers. Also disclosed are methods of making elastomeric articles, methods of reducing mold fouling, elastomeric compositions, and elastomeric articles made from elastomeric compositions.
    公开号:BR112015022755B1
    申请号:R112015022755-4
    申请日:2014-02-28
    公开日:2020-07-21
    发明作者:Wayne Ranbom；Leonard H. Palys
    申请人:Arkema Inc.；
    IPC主号:
    专利说明:

    [0001] [0001] The present invention relates to methods for crosslinking polymer compositions in the presence of atmospheric oxygen and to products manufactured using these methods. BACKGROUND OF THE INVENTION
    [0002] [0002] Polymers and copolymers cross-linked with free radical initiators, organic peroxides and / or azo initiators are known to have superior properties, particularly compared to cross-linked polymers by means of sulfur curing. These properties include high resistance to heat aging, low compression, reduced coloration of metallic or metal-coated sheets, and ease of producing colored products that have color stability during crosslinking and for long periods of use. These properties make use of peroxide cure, of great practical importance. A possible disadvantage of curing polymers with free radicals of organic peroxides and azo initiators has been that if air is not excluded from the material surface during curing, a sticky surface may result due to inhibition of curing by oxygen in the air.
    [0003] [0003] In order to avoid sticky surfaces on objects manufactured using such cross-linking with free radicals by means of organic peroxides and / or azo initiators, it has been conventional to exclude air from contact with the surface during curing to avoid inhibition of cure caused by the presence of oxygen. Measures to exclude oxygen increase the cost and complexity of the curing step, and it is sometimes difficult, as in the case of curing in steam autoclaves and inside tubes, to ensure complete exhaustion of air and oxygen. In some cases, the manufacturer would like to switch from sulfur curing to peroxide curing, and to use curing chambers in existing hot air furnaces. Curing with conventional peroxide systems, under these circumstances, would not be feasible as it would result in a sticky surface.
    [0004] [0004] U.S. Patent No. 6,747,099, which is incorporated herein in its entirety as a reference, has disclosed compositions to provide a surface free of adhesion by cure.
    [0005] [0005] In order to simplify and reduce the cost and complexity of the curing step, several methods have been suggested to prevent inhibition of the surface cure by oxygen during cross-linking with free radicals. These methods have, for various reasons, had little or no success in practical reality. In particular, none of them provided an adhesive-free surface, while providing the most desirable physical property of peroxide (azo) curing; a compression greater than 150 ° C for 70 hours, compared to about 100 ° C, i.e., a performance at a lower temperature for the state of the art.
    [0006] [0006] Thus, it is desirable to have methods for curing polymers and copolymers, which can be performed in the total or partial presence of atmospheric oxygen. It is also desirable to have elastomeric compositions that can be molded and do not stick to the mold. SUMMARY OF THE INVENTION
    [0007] [0007] The present invention relates to methods for crosslinking polymer compositions with total or partial contact with atmospheric oxygen, and in the presence of an organic peroxide formulation. In addition to at least one organic peroxide, the formulation of organic peroxides can comprise at least one additional compound chosen from superior bis, tri and polymaleimides, superior bis, tri and polycitraconimides, peroxide-crosslinkable silicone elastomers, anti-zonants based on p- phenylenediamines, and sulfur-containing organic compounds that are sulfur curing accelerators (crosslinking) of sulfur curable / crosslinkable polymers, and also sulfur compounds that are polysulfide polymers. The invention also relates to compositions containing the crosslinkable polymer compositions, and to products produced by such processes.
    [0008] A) a mistura de pelo menos um elastômero, pelo menos um polímero, e pelo menos uma formulação de peróxidos orgânicos para proporcionar uma mistura, em que o elastômero é saturado ou insaturado, o polímero é saturado ou insaturado, e o referido polímero não compreende polietileno clorado ou polietileno clorossulfonado; e em que a formulação de peróxidos orgânicos compreende i) pelo menos um peróxido orgânico, ii) pelo menos uma unidade escolhida de bis, tri e polimeleimidas superiores, bis, tri e policitraconimidas superiores, e antiozonantes à base de p- fenilenodiaminas, e iii) pelo menos um acelerador de enxofre; e B) a cura da referida mistura na presença de oxigênio. [0008] At least one embodiment of the present invention relates to a process for curing an elastomer composition in the presence of oxygen comprising: A) mixing at least one elastomer, at least one polymer, and at least one formulation of organic peroxides to provide a mixture, wherein the elastomer is saturated or unsaturated, the polymer is saturated or unsaturated, and said polymer does not comprise chlorinated polyethylene or chlorosulfonated polyethylene; and wherein the formulation of organic peroxides comprises i) at least one organic peroxide, ii) at least one unit chosen from superior bis, tri and polyimelimides, superior bis, tri and polycitraconimides, and antiozonants based on p-phenylenediamines, and iii ) at least one sulfur accelerator; and B) curing said mixture in the presence of oxygen.
    [0009] A) pelo menos um elastômero que é saturado ou insaturado; B) pelo menos um polímero que é saturado ou insaturado; C) pelo menos um peróxido orgânico; D) pelo menos um composto escolhido de bis, tri e polimaleimidas superiores, e bis, tri e policitraconimidas superiores; e E) pelo menos um acelerador de enxofre; em que o pelo menos um polímero não compreende polietileno clorado ou polietileno clorossulfonado. [0009] The modalities of the present invention also refer to a curable elastomer composition in the presence of oxygen, comprising said composition: A) at least one elastomer that is saturated or unsaturated; B) at least one polymer that is saturated or unsaturated; C) at least one organic peroxide; D) at least one compound chosen from higher bis, tri and polymalimides, and higher bis, tri and polycitraconimides; and E) at least one sulfur accelerator; wherein the at least one polymer does not comprise chlorinated polyethylene or chlorosulfonated polyethylene.
    [0010] [0010] Other embodiments of the present invention relate to a method of making an article comprising an elastomer composition, as described herein, comprising: extruding said elastomer composition in the presence of hot air to form an uncured preformed article; and curing the uncured preformed article.
    [0011] A) o fornecimento de uma composição de elastômeros não curada a um molde, em que a composição de elastômeros não curada compreende pelo menos uma formulação de peróxidos orgânicos; B) a cura da composição de elastômeros para formar um artigo elastomérico; e C) a liberação do artigo elastomérico curado do molde. [0011] The modalities of the present invention also refer to a process to reduce molding fouling in the presence of oxygen during the manufacture of elastomeric articles, comprising: A) providing an uncured elastomer composition to a mold, wherein the uncured elastomer composition comprises at least one formulation of organic peroxides; B) curing the elastomer composition to form an elastomeric article; and C) releasing the cured elastomeric article from the mold.
    [0012] [0012] The embodiments of the present invention also refer to elastomeric compositions comprising a formulation of organic peroxides, and to products manufactured using the above methods. BRIEF DESCRIPTION OF THE FIGURES
    [0013] [0013] FIG. 1 shows a comparison of two samples of a poly (ethylenepropylene) elastomer.
    [0014] [0014] FIG. 2 shows a comparison of two samples of a poly (ethylenepropylenediene) elastomer.
    [0015] [0015] FIG. 3 shows a comparison of two samples of a mixture of elastomers of poly (ethylenepropylene) and poly (ethylenepropylenediene). DETAILED DESCRIPTION
    [0016] [0016] One aspect of the present disclosure relates to a process for curing an elastomer composition, which comprises curing an elastomer composition comprising at least one elastomer used alone or in combination with at least one polymer, in full or partial presence of atmospheric oxygen, and in the presence of a formulation of organic peroxides.
    [0017] [0017] As used herein, the term "polymer" means a non-elastomeric / non-elastic polymer, which comprises at least one monomer. The term "polymer" encompasses homopolymers and copolymers, where the term "copolymers" refers to a non-elastomeric / non-elastic polymer, which comprises at least two different monomers in the polymerized form. For example, a copolymer according to the present disclosure can be a polymer comprising two different monomers, a terpolymer comprising three different monomers, or a polymer comprising more than three different monomers.
    [0018] [0018] As used herein, the term "cure" refers to the crosslinking of polymeric chains to form a reinforced or hardened polymer.
    [0019] [0019] In at least one embodiment, the composition of elastomers may comprise a saturated elastomer, an unsaturated elastomer, or both a saturated and unsaturated elastomer.
    [0020] Similarly, the at least one polymer of the elastomer composition may comprise a saturated polymer, an unsaturated polymer, or both a saturated and unsaturated polymer.
    [0021] [0021] In at least one embodiment, the polymer of the elastomer composition comprises a copolymer. The modalities disclosed in this document recite elastomeric compositions that comprise a copolymer. However, as a person skilled in the art will readily appreciate, a homopolymer may be substituted in any embodiment comprising a copolymer, unless expressly stated otherwise.
    [0022] [0022] In at least one embodiment, the elastomer composition comprises at least one elastomer and at least one copolymer. The elastomer and copolymer can be present in the composition of elastomers in weight ratios ranging from 99: 1 to 1:99, such as, for example, from 85:15 to 15:85, or from 75:25 to 25: 75. In at least one embodiment, the elastomer and copolymer are present in the elastomer composition in a 50:50 weight ratio.
    [0023] [0023] According to at least one embodiment, the composition of elastomers comprises at least one saturated elastomer. The saturated elastomer can be selected, for example, from an ethylene-propylene terpolymer (EPDM), fluoroelastomers (FKM, FFKM, FVMQ) (eg, Viton® and Dyneon®), vinyl silicone rubber (VMQ), and their combinations.
    [0024] [0024] Unsaturated elastomers that can be used in the composition of elastomers include, for example, nitrite rubber (NBR), acrylonitrile-butadiene-styrene (ABS), styrene-butadiene rubber (SBR), styrene-butadiene block copolymers -styrene (SBS), polybutadiene rubber (BR), styrene-isoprene-styrene block copolymers (SIS), halogenated acrylonitrile-butadiene (HNBR), natural rubber (NR), polyisoprene synthetic rubber (IR), rubber neoprene (CR), polychloropropene, bromobutyl rubber, chlorobutyl rubber, and their combinations.
    [0025] [0025] According to at least one embodiment, the composition of elastomers comprises at least one unsaturated polymer. Non-limiting examples of unsaturated polymers that can be used include copolymers of ethylene with propylene, butylene, pentene, hexane, heptane, octane, and vinyl acetate, such as linear low density polyethylene (LLDPE), low density polyethylene (LDPE ), high density polyethylene (HDPE), poly (ethylene-vinyl acetate) (EVA), poly (ethylene-propylene) (EPM), poly (ethylene-octene) (Engage®), poly (ethylene-hexene) ( Insite Technology®), poly (ethylene-butylene) Tafmer®, Vamac® polymers (poly (ethylene-methyl acrylate), poly (ethylene-acrylate), and combinations with acrylic acid), and their combinations.
    [0026] [0026] In at least one embodiment, the composition of elastomers does not comprise chlorinated polyethylene or chlorosulfonated polyethylene.
    [0027] [0027] When a foam product is desired, the elastomer composition may comprise a blowing agent.
    [0028] [0028] The curing or crosslinking step can be carried out in any conventional manner, such as, for example, by molding with hot air, steam, and hot.
    [0029] [0029] The formulation of organic peroxides comprises at least one organic peroxide. With the exception of hydroperoxides and liquid peroxydicarbonates, all organic peroxides known to undergo decomposition by heat to generate radicals capable of initiating the desired healing reactions (crosslinking) are contemplated as suitable for use in the present disclosure. Non-limiting examples include dialkyl peroxides, diperoxicetals, monoperoxycarbonates, cyclic ketone peroxides, diacyl peroxides, organosulfonyl peroxides, peroxyesters and solid peroxydicarbonates, stable at room temperature. In at least one embodiment, organic peroxide is selected from dialkyl peroxides, peroxycetals, cyclic ketone peroxides and diacyl peroxides.
    [0030] [0030] Names of peroxides and physical properties for all these classes of organic peroxides can be found in "Organic Peroxides" by Jose Sanchez and Terry N. Myers; Kirk-Othmer Encyclopedia of Chemical Technology, Fourth Ed., Volume 18, (1996).
    [0031] [0031] Illustrative dialkyl peroxide initiators include: di-t-butyl peroxide; t-butylcumyl peroxide; 2.5-di (cumylperoxy) -2,5-dimethylhexane; 2.5-di (cumylperoxy) -2,5-dimethyl-3-hexino; 4-methyl-4- (t-butylperoxy) -2-pentanol; 4-methyl-4- (t-amylperoxy) -2-pentanol; 4-methyl-4- (cumylperoxy) -2-pentanol; 4-methyl-4- (t-butylperoxy) -2-pentanone; 4-methyl-4- (t-amylperoxy) -2-pentanone; 4-methyl-4- (cumylperoxy) -2-pentanone; 2.5-dimethyl-2,5-di (t-butylperoxy) hexane; 2.5-dimethyl-2,5-di (t-amylperoxy) hexane; 2,5-dimethyl-2,5-di (t-butylperoxy) -3-hexino; 2.5-dimethyl-2,5-di (t-amylperoxy) -3-hexino; 2.5-dimethyl-2-t-butylperoxy-5-hydroperoxyhexane; 2.5-dimethyl-2-cumylperoxy-5-hydroperoxyhexane; 2.5-dimethyl-2-t-amylperoxy-5-hydroperoxyhexane; m / p-alpha, alpha-di [(t-butylperoxy) isopropyl] benzene; 1.3.5- tris (t-butylperoxyisopropyl) benzene; 1.3.5- tris (t-amylperoxyisopropyl) benzene; 1.3.5- tris (cumylperoxyisopropyl) benzene; di [1,3-dimethyl-3- (t-butylperoxy) butyl carbonate]; di [1,3-dimethyl-3- (t-amylperoxy) butyl carbonate]; di [1,3-dimethyl-3- (cumylperoxy) butyl carbonate]; di-t-amyl peroxide; t-amylcumyl peroxide; 2.4.6- tri (butylperoxy) -s-triazine; 1.3.5- tri [1- (t-butylperoxy) -1-methylethyl] benzene 1.3.5- tri - [(t-butylperoxy) -isopropyl] benzene; 1.3-dimethyl-3- (t-butylperoxy) butanol; 1.3-dimethyl-3- (t-amylperoxy) butanol; and their mixtures.
    [0032] [0032] Illustrative solid peroxydicarbonates, stable at room temperature, include, but are not limited to: di (2-phenoxyethyl) peroxydicarbonate; di (4-t-butyl-cyclohexyl) peroxydicarbonate; dimyristyl peroxydicarbonate; dibenzyl peroxydicarbonate; and di (isobornyl) peroxydicarbonate.
    [0033] [0033] Another class of dialkyl peroxides that can be used alone or in combination with the other free radical initiators contemplated by the present disclosure, are those selected from the group represented by the formula:
    [0034] [0034] Other dialkyl peroxides include: 3-cumylperoxy-1,3-dimethylbutyl methacrylate; 3-t-butylperoxy-1,3-dimethylbutyl methacrylate; 3-t-amylperoxy-1,3-dimethylbutyl methacrylate; tri (1,3-dimethyl-3-t-butylperoxybutyloxy) vinylsilane; 1,3-dimethyl-3- (t-butylperoxy) butyl N- [1- {3- (1-methylethyl) -phenyl} 1-methylethyl] carbamate; 1,3-Dimethyl-3- (t-amylperoxy) N-[1- {3- (1-methylethyl) -phenyl} -1-methylethyl] carbamate; 1,3-dimethyl-3- (cumylperoxy) butyl N- [1- {3- (1-methylethyl) -phenyl} -1-methylethyl] carbamate;
    [0035] [0035] In the group of diperoxicetal initiators, preferred initiators include: 1.1- di (t-butylperoxy) -3,3,5-trimethylcyclohexane; 1.1- di (t-butylperoxy) cyclohexane; N-butyl 4,4-di (t-amylperoxy) valerate; 3.3-ethyl di (t-butylperoxy) butyrate; 2.2-di (t-amylperoxy) propane; 3,6,6,9,9-pentamethyl-3-ethoxyabonylmethyl-1,2,4,5-tetraoxacyclononane; 4.4-n-butyl bis (t-butylperoxy) valerate; 3.3-ethyl di (t-amylperoxy) butyrate; and their mixtures.
    [0036] [0036] Other peroxides that can be used according to at least one embodiment of the present disclosure include benzoyl peroxide, OO-t-butyl-O-hydrogen-monoperoxy-succinate and OO-t-amyl-O-hydrogen-monoperoxy -succinate.
    [0037] [0037] Illustrative cyclic ketone peroxides are composed with the general formulas (I), (II) and / or (III).
    [0038] [0038] Some examples of suitable peroxides of cyclic ketones include: 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxinonane (or methyl ethyl ketone cyclic trimer), methyl ethyl ketone cyclic dimer, and 3,3,6,6,9 , 9-hexamethyl-1.2.4.5-tetraoxycyclononane.
    [0039] [0039] Illustrative examples of peroxyesters include: 2.5-dimethyl-2,5-di (benzoylperoxy) hexane; t-butyl perbenzoate; t-butyl peroxyacetate; t-butylperoxy-2-ethyl hexanoate; t-amyl perbenzoate; t-amyl peroxyacetate; t-butyl peroxyisobutyrate; 3-hydroxy-1,1-dimethyl t-butylperoxy-2-ethylhexanoate; OO-t-amyl-O-hydrogen-monoperoxysuccinate; OO-t-butyl-O-hydrogen-monoperoxysuccinate; di-t-butyl diperoxiftalate; t-butylperoxy (3,3,5-trimethylhexanoate); 1,4-bis (t-butylperoxycarb) cyclohexane; t-butylperoxy-3,5,5-trimethyl hexanoate; t-butyl peroxy- (cis-3-carboxy) propionate; Allyl 3-methyl-3-t-butylperoxybutyrate.
    [0040] [0040] Illustrative monoperoxycarbonates include: OO-t-butyl-O-isopropylmonoperoxycarbonate; OO-t-butyl-O- (2-ethylhexyl) monoperoxycarbonate; 1.1.1- tris [2- (t-butylperoxy-carbonyloxy) ethoxymethyl] propane; 1.1.1- tris [2- (t-amylperoxy-carbonyloxy) ethoxymethyl] propane; 1,1,1-tris [2- (cumylperoxy-cabonyloxy) ethoxymethyl] propane; OO-t-ami1-O-isopropylmonoperoxycarbonate.
    [0041] [0041] Illustrative diagonal peroxides include: di (4-methylbenzoyl) peroxide; di (3-methylbenzoyl) peroxide; di (2-methylbenzoyl) peroxide; didecanoyl peroxide; dilauroyl peroxide; 2,4-dibromo-benzoyl peroxide; succinic acid peroxide; dibenzoyl peroxide; di (2,4-dichlorobenzoyl) peroxide.
    [0042] [0042] Imido peroxides of the type described in PCT application publication WO97 03961 A1, of 6 February. 1997, are also considered useful for use.
    [0043] [0043] The formulation and / or mixture of organic peroxides can also comprise at least one additional compound chosen from substances including higher bis, tri and polymaterials, higher bis, tri and polycitraconimides, such as p-phenylenediamines, organic compounds sulfur containing accelerators for sulfur curing (crosslinking) of sulfur curable / crosslinkable polymers and polysulfide polymers. In at least one embodiment, the formulation and / or mixture of organic peroxides can also comprise an azo initiator.
    [0044] [0044] In at least one embodiment, the formulation of organic peroxides comprises a maleimide compound of Formula IV:
    [0045] [0045] One skilled in the art will recognize that the other compounds that fall within the scope of Formula IV are all solid materials, are all trimaleimides, bismaleimides, tricitraconimides, or biscitraconimides, and can all be combined with the compounds of the organic peroxide formulation. . Bismaleimides and biscitraconimides are all commercially available or can be readily synthesized by methods well known in the art. See, for example, U.S. Pat. No. 5,494,948, 5,616,666, 5,292,815 and the references cited therein for synthetic methods, each of which is incorporated herein in its entirety.
    [0046] [0046] Trimaleimides and tricitraconimides, as well as superior polyimaleides and citraconimides, can be prepared by similar techniques if they are not commercially available. For example, trimaleimide, N, N ', N "- (1,3,5-triazine-2,4,6-triyl) trimaleimide has CAS number CAS (67460-81-5).
    [0047] [0047] Some primary amines suitable for the synthesis of superior di, tri and polymaleimides and citraconimides analogues are polyfunctional primary amines such as melamine, various polyoxypropylene amines such as polyoxypropylenediamines and polyoxypropylenetriamines sold under the trade name JEFFAMINE by Huntsman Corporation.
    [0048] [0048] In addition to the N, N'-m-phenylene-bismaleimide specifically mentioned above, other bismaleimides, in addition to those disclosed in the above mentioned patents, suitable for use in the formulation of organic peroxides, without limiting the generality of the general Formula (IV ) above are: N, N'-ethylenebismaleimide, N, N'-hexamethylenebismaleimide, N, N'-dodecamethylenebismaleimide, N, N '- (2,2,4-trimethylhexamethylene) bismaleimide, N, N' - (oxy-dipropylene) bismaleimide , N, N '- (aminodipropylene) bismaleimide, N, N' - (ethylenedioxy-dipropylene) bismaleimide, N, N '(1,4-cyclohexylene) bismaleimide, N, N' - (1,3-cyclohexylene) bismaleimide, N, N '- (methylene-1,4-dicyclohexylene) bismaleimide, N, N' - (isopropylidene-1,4-dicyclohexylene) bismaleimide, N, N '- (oxy-1,4-dicyclohexylene) bismaleimide, N, N'-p- (phenylene) bismaleimide, N, N '- (o-phenylene) bismaleimide, N, N' - (1,3-naphthylene) bismaleimide, N, N '- (1,4-naphthylene) bismaleimide, Ν, Ν '- (1,5-naphthylene) bismaleimide, N, N- (3,3'-dimethyl-4,4'-diphenylene) bismaleimide, N, N '- (3,3-dichloro-4,4 '-biphenylene) bismaleimide, N, N' - (2,4-pyridyl) bismaleimide, N, N (2,6-pyridyl) bismaleimide, N, N '- (1,4-anthraquinonodiil) bismaleimide, N, N' - (m-tolylene) bismaleimide, N, N (p-tolylene) bismaleimide, N, N '- (4,6-dimethyl-1,3-phenylene) bismaleimide, N, N' - (2,3-dimethyl- 1,4-phenylene) bismaleimide, N, N '- ( 4,6-dichloro-1,3-phenylene) bismaleimide, N, N '- (5-chloro-1,3-phenylene) bismaleimide, N, N' - (5-hydroxy-1,3-phenylene) bismaleimide, N, N '- (5-methoxy-1,3-phenylene) bismaleimide, N, N (m-xylylene) bismaleimide, N, N' - (p-xylylene) bismaleimide, N, N '- (methylenedi-p- phenylene) bismaleimide, N, N '- (isopropylidenodi-p-phenylene) bismaleimide, N, N' - (oxy-p-phenylene) bismaleimide, N, N '- (thiodi-p-phenylene) bismaleimide, N, N' - (dithiodi-p-phenylene) bismaleimide, N, N '- (sulfodi-p-phenylene) bismaleimide, N, N' - (carbonyldi-p-phenylene) bismaleimide, α, α-bis- (4-maleimodophenyl) - meta-diisopropylbenzene, α, α-bis- (4-p-phenylene) bismaleimide and α, α-bis- (4-maleimidophenyl) para-diisopropylbenzene.
    [0049] [0049] Combinations of two or more bismaleimides, or bismaleimides with the trimaleimides, and with the superior polyimaleids in the compositions and processes of the invention are also contemplated as equivalents, and one skilled in the art will understand that such tripolymeimides and superior polyimaleids, and their substitution by the compounds and processes specifically illustrated in the present document for the practice of the invention to be such equivalents and to be well within the scope, are contemplated by the invention.
    [0050] [0050] Biscitraconimides, which can be replaced in whole or in part by the N, N'-m-phenylenebismaleimide mentioned above, include as representative examples: 1.2- N, N'-dimethylenebiscitraconimide; 1.2- N, N'-trimethylenebiscitraconimide; 1,5-N, N'-2-methylpentamethylene) -biscitraconimide; and N, N'-methylphenylenebiscitraconimide.
    [0051] [0051] Mixtures of biscitraconimides and mixtures of bismaleimides and biscitraconimides may also be used, as well as those that include trimaleimides in the formulation of organic peroxides.
    [0052] [0052] Biscitraconimides are well known compounds, and when they are not commercially available, they can be readily synthesized by methods detailed in the art. U.S. Pat. No. 5,292,815 in column 4, provides a detailed list of such methods. As mentioned above, tripolycitraconimides and higher polycitraconimides can be prepared by analogous methods and substituted in whole or in part in the formulation of organic peroxides of the present disclosure, and such compounds and substitutions will be understood by a person skilled in the art as being a complete equivalent of specifically illustrated in this document, and well within the scope contemplated as equivalent by the invention.
    [0053] [0053] According to at least one embodiment, the formulation of organic peroxides can also comprise a silicone elastomer. Silicone elastomers that can be used in the formulation of organic peroxides include, for example, unsaturated silicone elastomers crosslinkable with peroxides comprising at least one unsaturation site (such as a vinyl group) per molecule. In one embodiment, the silicone elastomer comprises a plurality of unsaturation sites. An exemplary class of peroxide crosslinkable silicone elastomers comprises elastomers derived from dimethyl vinyl substituted silicone, which are well known in the art. See, for example, "Kirk Othmer Encyclopedia of Chemical Technology", Vol. 20, p. 943 et seq., John Wiley & Sons, © 1982, incorporated herein.
    [0054] [0054] In at least one embodiment, the formulation of organic peroxides also comprises a sulfur-containing organic compound capable of accelerating sulfur vulcanization of polymers, which can be cross-linked with sulfur. Exemplary organic compounds containing sulfur, capable of accelerating sulfur vulcanization of polymers, are well known in the art. Many different classes of these compounds are known and all of them are considered to be equivalent.
    [0055] [0055] The book "The Vanderbilt Rubber Handbook", thirteenth edition, 1990, editor R.T. Vanderbilt Company, Inc., lists many types. Illustrative of these are derivatives of benzothiazoles, thiadiazoles, sulfenamides, sulfenimides, dithiocarbamates, thiuramas, imidazoles, xanthates, and thioureas. Also included in this general class are sulfur accelerators of sulfur compounds, sulfides, disulfides (e.g., diallyldisulfides) polysulfides and arylpolysulfide compounds such as amylphenol polysulfides, e.g. ex. VULTAC® products from Arkema, and other sulfides such as disulfides and / or other known sulfur-accelerating polysulfide phosphates, dithiophosphates and / or compounds containing phosphorus and sulfur. Other sulfur-containing organic compounds, capable of donating sulfur at vulcanization temperatures, which are known but which are not currently used for such reactions due to cost issues, are also contemplated as equivalent. Illustrative of these is the compound 2- (2,4-cyclopentadiene-1-ylidene) -1,3-dithiolane.
    [0056] [0056] In at least one embodiment, a class of sulfur accelerators includes salts of disubstituted dithiocarbamic acid.
    [0057] [0057] These salts have the general structure:
    [0058] [0058] Examples of the disubstituted dithiocarbamic acid salts include: bismuth dimethyldithiocarbamate; cadmium diethyldithiocarbamate; cadmium diamldithiocarbamate; copper dimethyldithiocarbamate; lead diamildithiocarbamate; lead dimethylthiocarbamate; selenium diethyldithiocarbamate; selenium dimethyldithiocarbamate; tellurium diethyldithiocarbamate; piperidinium pentamethylenediocarbamate; zinc diamildithiocarbamate; zinc diisobutyldithiocarbamate zinc diethyldithiocarbamate; zinc dimethyldithiocarbamate; copper dibutyldithiocarbamate; sodium dimethyldithiocarbamate; sodium diethyldithiocarbamate; sodium dibutyldithiocarbamate; zinc di-n-butyldithiocarbamate; zinc dibenzyldithiocarbamate.
    [0059] [0059] A second class of sulfur accelerators suitable for use in the formulation of organic peroxides comprises thiuramas. These are prepared from secondary amines and carbon disulfide, and have the general structure:
    [0060] [0060] Examples of sulfur and thiurama accelerators include: tetrasulfide and hexasulfide of dipentamethylenethiurama; tetrabutylthiurama disulfide; tetramethylthiurama disulfide; tetraethylthiurama disulfide; tetramethylthiurama monosulfide; isobutylthiurama disulfide; dibenzylthiurama disulfide; tetrabenzylthiurama disulfide; tetraisobutylthiurama disulfide; isobutylthiurama monosulfide; dibenzylthiurama monosulfide; tetrabenzylthiurama monosulfide; tetraisobutylthiurama monosulfide.
    [0061] [0061] The superior multisulfides of the various thiouramas are also donors of sulfur.
    [0062] [0062] Thiadiazole derivatives are, but are not limited to, dimercaptothiadiazole monobenzoyl derivatives (2,5-dimethyl-1,3,4-thiadiazole); patented thiadiazole from The Vanderbilt Rubber Company, identified as VANAX® 189; 1,2,4-thiadiazole, 5-ethoxy-3- (trichloromethyl) thiadiazole; and alkyl mercaptothiadiazoles, e.g. ex. methylmercaptotiadiazole.
    [0063] [0063] Benzothizole derivatives have the general structure:
    [0064] Illustrative compounds include: 2- (4-morpholinodithio) benzothiazole; benzothiazila disulfide; 2-mercapto-benzothiazole; 2-mercaptobenzothiazole disulfide; Sodium 2-mercaptobenzothiazolate; zinc-2-mercapto-benzothiazole; Copper 2-mercaptobenzothiazolate; 2-N-cyclohexylaminobenzothiazole; N-cyclohexylamino-2-benzothiazole polysulfide; 2-bisbenzothiazole-2, 2-polysulfide and 2-bisbenzothiazole-2,2-disulfide; bis (2,2'-benzothiazyldisulfide).
    [0065] [0065] Sulfenamide accelerators are also well known. Illustrative examples include: N-oxyethylene-2-benzothiazolsulfenamide; N-oxyethylenethiocarbamyl-N-oxyethylenesulfenamide; N-cyclohexyl-2 benzothiazolosulfenamide; N-t-butyl-2-benzothiazolosulfenamide; N-cyclohexyl-2-benzothiazilsulfenamide; N, N-dicyclohexylbenzothiazilsulfenamide; N-t-butyl-2-benzothiazolosulfenamide. There are also sulfenimide compounds, e.g. , N-t-butyl-benzothiazolo-2-sulfenimide.
    [0066] [0066] Typical imidazoles include: 2-mercaptobenzimidazole, 2-mercaptomethylbenzimidazole; and the zinc salt of 2-mercaptobenzimidazole.
    [0067] [0067] Zinc isopropylxanthate is a typical xanthate and sulfur accelerator.
    [0068] [0068] Typical thiourea include: trimethyl thiourea; 1,3-diethylthiourea and 1,3-dibutylthiourea; ethylene thiourea; mixture of dialkylthioureas; diphenylthiourea; diortotoliltiourea; dimethylthiourea; dibutyltiourea; dietiltiourea.
    [0069] [0069] Types of alkylphenoldisulfides of sulfur accelerators are illustrated by the compounds available from Arkema, under the designation VULTAC® 2, VULTAC® 3 and VULTAC® 5.
    [0070] [0070] Thiophosphate and sulfur accelerators are illustrated by compounds such as copper dialkyldithiophosphate compounds; zinc dialkyldithiophosphate; zinc aminodithiophosphate; zinc dibutyldithiophosphate; Copper O, diisopropyl phosphorodithiolate; and zinc O, O-diisopropylphosphorodithiolate.
    [0071] [0071] Other miscellaneous sulfur accelerators include 4,4-dithiodimorpholine; the N, N'-caprolactam disulfide; and dibutylxanthogen disulfide.
    [0072] [0072] In at least one embodiment, the formulation of organic peroxides also comprises an azo initiator. Azo initiators are those known in the art, such as 2,2'-azobis- (2-acetoxypropane), to generate free radicals by decomposition by heat, capable of inducing the desired curing (crosslinking) reaction. The azo primers of Pat. No. 3,862,107 and 4,129,531, the disclosures of which are hereby incorporated by reference, are also suitable.
    [0073] [0073] A person skilled in the art will readily be able to select adequate amounts of the various ingredients for use in the formulation of organic peroxides, and will be quickly and easily able to optimize concentrations through a series of laboratory-scale tests, employing increasing amounts of the ingredients. in samples of the polymer to be cured (cross-linked). The optimal time and temperatures, and similar processing conditions (combination) can also be determined from the same tests, as will the optimal cure time and temperature.
    [0074] [0074] In at least one embodiment, the compounds of Formula (IV) (bismaleimides and biscitraconimides) are present in the formulation of organic peroxides in amounts that will provide about 0.2 parts by weight per part of polymer by weight (phr ) at about 10.0 phr, such as from about 1.0 phr to about 5.0 phr, or from about 1.5 phr to about 3.0 phr.
    [0075] [0075] In at least one embodiment, the organic compound (s) containing sulfur capable of accelerating sulfur vulcanization in polymers capable of being crosslinked by sulfur are present in the formulation of organic peroxides in quantities that will deliver from about 0.01 phr to about 20 phr, such as from about 0.1 to about 10 phr, such as from about 0.1 phr to about 5 phr, such as from about 0.1 phr to about 1.0 phr, or from about 0.1 phr to about 0.5 phr. It is understood by those skilled in the art that these compounds are of two types, those that donate sulfur to vulcanization and those that simply accelerate sulfur vulcanization. Any of the classes of compounds or mixtures thereof are contemplated as equivalent by the invention.
    [0076] [0076] Alkylphenol disulfide polymers of the type sold by the company Arkema under the trade name VULTAC® can be used in quantities of about 0.5 phr to 20 phr when used alone, or from about 0.1 phr to about 10 phr when in combination with other sulfur accelerators.
    [0077] [0077] In at least one embodiment, the organic peroxide and optional azo initiator is present in the formulation of organic peroxides in amounts from about 0.04 to about 10 phr, such as from about 0.1 to about 5 phr , such as from about 1 to about 4 phr.
    [0078] [0078] The time-temperature conditions required for curing depend largely on the structure of the free radical curing agent. For azo starters, the appropriate conditions are detailed in Pat. No. 3,632,107 and 4,129,531, each of which is incorporated herein in its entirety.
    [0079] [0079] For the elastomer compositions of the present disclosure, the appropriate time and temperature conditions can be determined by cross-linking a particular polymer composition by performing a small number of well-controlled rheometric studies and selecting values from the results of those studies, where the time / temperature ratio is five to fifteen times the half-life value for the free radical initiator in the system.
    [0080] [0080] In at least one embodiment, other conventional additives such as antioxidants (eg, phenol derivatives and polymeric quinoline derivatives), aliphatic oils may also be present in the elastomer compositions before, after and during the curing stage. processing, and other process aids, pigments, dyes, adhesives, waxes, reinforcement aids, UV stabilizing agents, blowing agents and activators and anti-zonants.
    [0081] [0081] Polysulfide polymers in at least one embodiment of the present disclosure, are known polysulfide polymers that are prepared by reacting an α, ω-dihaloalkyl (or dihaloheteroalkyl) compound with a metallic polysulfide, such as a polysulfide of a alkali metal. Common commercially available polysulfide polymers are liquid or solid, terminate with thiol or hydroxy groups, and are derived from materials produced by the reaction of 1,2-dichloroethane, 2,2'-dichlorodiethylether or bis (2-chloroethyl) formal with a alkali metal polysulfide (MSX), where M is an alkali metal ion, such as sodium derivatives, ex is a number greater than 1 and up to about six.
    [0082] [0082] The invention contemplates that polysulfide polymers can be used in place of, or when mixed with, compounds chosen from antiozonants based on p-phenylenediamines and organic compounds containing sulfur, selected from the group consisting of organic compounds containing sulfur capable of accelerate sulfur vulcanization of polymers capable of being crosslinkable with sulfur ("sulfur accelerators"), polysulfide polymers and mixtures of said sulfur-containing compounds in amounts equal to those previously specified for those compounds. Since an excess of polysulfide polymer is not considered to be harmful to the practice of the invention, it is also contemplated that they can be premixed with the compounds of Formula (IV) (bismaleimide and biscitraconimides) and optionally with the (s) free radical initiator (s) to form standard mixtures, either solid or liquid. Polysulfide polymers can also be pre-mixed in the polymer to be cured and with the compounds of Formula (IV), and the free radical initiator (s) can also be mixed simultaneously or later, according to the operator option. The use of polysulfide polymers in combination with the other sulfur may allow for a reduction in the amount of sulfur accelerator used.
    [0083] [0083] In at least one embodiment of this disclosure, the formulation of organic peroxides comprises at least one organic peroxide and a) at least one compound (A) selected from the group consisting of silicone elastomers and a compound of formula (I):
    [0084] [0084] In at least one embodiment of the present disclosure, the organic peroxide formulation comprises a mixture of dipentamethylenethiurama tetrasulfide (such as SULFADS®), N, N'-m-phenylenebismaleimide (such as HVA-2) and 1.1 -di (t-butylperoxy) -3,3,5-trimethylcyclohexane (such as LUPEROX® 231 XL), which can be used to cure an ethylene-propylene copolymer (VISTALON® 504) in hot air.
    [0085] [0085] To prepare the mixture of SULFADS®, HVA-2 and LUPEROX 231 XL, the ingredients, which are all in the form of dry powder (LUPEROX® 231 XL is in the form of 40% by weight of peroxide dispersed in carbonate of calcium), can be mixed in any order and then combined by standard methods (Banbury, two-roller mill, extruder and the like) into the VISTALON® polymer. SULFADS®, HVA-2 and LUPEROX 231 XL can also be combined directly in VISTALON, simultaneously or sequentially in any order. Any two of the ingredients SULFADS®, HVA-2 and LUPEROX® 231 XL can be mixed and combined in VISTALON® separately or simultaneously with the third ingredient. This combination, if done separately, can also be done in any order of addition of the ingredients to the polymer, but it is preferable if the peroxide is added last.
    [0086] [0086] Once the combination with VISTALON® is finished, the combined mixture can be cured simply by placing it in a hot air oven at an appropriate temperature to start curing by decomposition of the peroxide, conveniently, in this case, about 365 ° F (about 185 ° C), for a period of time sufficient to allow the desired degree of crosslinking to take place, conveniently, in this case, about one minute, for a fine sample at room temperature in the beginning.
    [0087] [0087] At least one embodiment of the present disclosure relates to a method of manufacturing an article comprising the elastomer composition described above. In at least one embodiment, the article may comprise a seal, a hose or a gasket. The method may comprise extruding an elastomer composition, as described above, wherein the elastomer composition comprises an organic peroxide formulation to form an uncured preformed article, and curing the uncured preformed article. The elastomer composition can be extruded in the presence of hot air to form the uncured preform. In at least one embodiment, the preform is cured using a microwave or steam autoclave. In at least one other embodiment, the preform is cured without using a microwave or a steam autoclave.
    [0088] [0088] In at least one embodiment, the elastomer composition may comprise at least one unsaturated elastomer and at least one saturated elastomer.
    [0089] [0089] The method of manufacture of the article can be carried out in a hot air tunnel, or in any other known device.
    [0090] [0090] In at least one modality, the method of manufacture of the article can be formed continuously. Continuous fabrication may allow the production of a continuous article, such as a continuous seal, as opposed to seals that have to be assembled from smaller parts.
    [0091] [0091] The present disclosure also refers to automotive, industrial or residential seals, manufactured according to the methods disclosed in this document.
    [0092] [0092] At least one embodiment of the present disclosure relates to a method of making a hose. The method may comprise extruding a hose length from an elastomer composition without curing the hose length. The length of the uncured hose can be retracted and then cured, such as by exposing the uncured hose to steam.
    [0093] [0093] The present disclosure also refers to a process to reduce molding fouling in the presence of oxygen during the manufacture of elastomeric articles. In previous methods, the oxygen present in a mold prevented the complete reaction of the elastomer, leaving an uncured elastomer residue that formed in the mold. This formation needed to be cleaned periodically.
    [0094] [0094] In at least one embodiment, the present invention provides a process for reducing mold fouling in the presence of oxygen, which comprises providing an uncured elastomer composition to a mold, wherein the uncured elastomer composition comprises at least one formulation of organic peroxides. The elastomer composition can then be heated to a temperature sufficient to cure the elastomer composition to form an elastomeric article, following the release of the elastomeric article from the mold.
    [0095] [0095] The present disclosure also relates to a method of manufacturing an elastomeric article, which comprises at least one elastomer and at least one unsaturated polymer. The method may comprise extruding and curing an elastomer composition in the presence of hot air to form an elastomeric article, wherein the elastomeric composition comprises an organic peroxide formulation.
    [0096] [0096] Exemplary elastomeric articles that can be manufactured according to the methods of the present disclosure include O-rings, gaskets, diaphragms, seals, insulating rings, electrical insulators, shoe soles, septa, connections, films, sheets, belts, tubes , etc.
    [0097] [0097] The modalities described in this document are intended to be exemplary of the invention and not to limit it. One skilled in the art will appreciate that modifications can be made to the modalities and examples of the present disclosure without departing from the scope of the present disclosure. The modalities of the invention are described above using the term "comprising" and variations thereof. However, it is the inventors' intention that the term "comprising" can be replaced in any of the embodiments described herein by "consisting of" and "consisting essentially of", without departing from the scope of the invention.
    [0098] [0098] The following examples further illustrate the best way contemplated by the inventors for the practice of their invention, and are to be understood as illustrative and not as a limitation thereof. EXAMPLES
    [0099] [0099] Various peroxide-elastomer compositions were prepared and cured in a hot air oven at 215 ° C for 15 minutes.
    [0100] 1. Composição elastomérica de poli (etilenopropileno) (EPM) 2. Composição elastomérica de poli(etilenopropilenodieno) (EPDM) 3. Uma Mistura de Elastômeros de 54% de EPDM e 46% de EPM [0100] The peroxide-elastomer compositions studied were labeled "Control" or "AIR-NS", and are provided below. Three elastomers were studied and discussed in the order that follows. 1. Elastomeric composition of poly (ethylenepropylene) (EPM) 2. Elastomeric composition of poly (ethylenepropylene diamine) (EPDM) 3. A blend of elastomers of 54% EPDM and 46% EPM
    [0101] [0101] Uncured flat sheets of the elastomer-peroxide compositions were hung with metal clips in a hot air oven set at 215 ° C and cured for 15 minutes. After 15 minutes, the cured samples were quickly removed from the air oven, placed on the bench and immediately a paper towel was pressed firmly against the very hot surface of the sheet for one minute. The paper towel was then removed from the cured elastomeric sheet. The cooled sample was mounted on labeled cardboard, so that a photograph of the surface could be taken. This was done to visually judge the composition's ability to create a non-stick surface, through the amount of fibers of the white paper towel that were glued to the surface. The elastomer samples were also tested for MH-ML (dN-m) for the relative degree of crosslinking performance using an RPA® Rheometer from Alpha Technologies.
    [0102] [0102] Photographs of elastomer-peroxide compositions that were cured in a hot air oven at 215 ° C for 15 minutes and immediately subjected to the surface cure test with a paper towel, are provided in FIG. 1. This paper towel test provides a very good indication of complete surface healing. Any areas where the surface of the elastomer is not completely cured will be quite sticky, and the paper towel fibers will adhere to the sticky, uncured surface of the elastomer composition.
    [0103] [0103] The "Control" composition using an EPM elastomer-peroxide mixture provided a very rough surface with considerable paper towel fibers adhered to the uncured sticky surface. The peroxide-elastomer composition labeled "AIR-NS" using EPM also resulted in an undesirable rough surface, albeit to a lesser extent than the "Control" composition. Noteworthy paper towel fibers were found for both samples, glued to the surface, indicating an uncured sticky surface. Uncured surface areas will be considered a serious defect in automotive gasket seals.
    [0104] [0104] The "Control" composition using an EPDM elastomer-peroxide mixture provided a very rough surface with many small paper towel particles stuck together, indicating a poor surface cure. The sample cured with the EPDM composition labeled "AIR-NS" is smooth, with some traces of paper towel fibers, which indicates a reasonably good surface cure. Photographs of the "Control" and "AIR-NS" samples for Example 2 are shown in FIG. 2.
    [0105] [0105] FIG. 3 shows the surface curing performance of peroxide-elastomer blend compositions using a blend of 54% EPDM and 46% EPM, labeled "Control". Unlike the EPM # 1 and EPDM # 2 photographs for "Control", this "Control" # 3 composition provided one of the poorest surface cures, with a considerable amount of paper towel fibers glued to a surface rough, poorly healed.
    [0106] [0106] In contrast, surprisingly, the new composition of this present invention, which comprises 54% EPDM and 46% EPM and the components of the invention labeled "AIR-NS", provided a very shiny surface without any fibers from the towel of paper glued to the surface, indicating excellent surface cure.
    [0107] [0107] Some air bubbles trapped in the uncured sample sheet were present before curing in the hot air oven, which appear as white reflective areas in FIG. 3 (due to the smooth and shiny surface of the sample). No paper towel fibers adhered to the surface were found, which indicates an excellent and complete cure of the surface. In summary, the new peroxide-elastomer composition # 3, as taught in this invention, which uses a new mixture of peroxide, additives, EPM and EPDM elastomers, provides an improved curing composition for the hot air curing process, in that an elastomeric surface completely free of adhesion is obtained, completely cured.
    权利要求:
    Claims (16)
    [0001]
    Process for curing an elastomer composition in the presence of oxygen, characterized by the fact that the process comprises the steps of: A) mixture of at least one elastomer comprising ethylene-propylene terpolymer, at least one non-elastic copolymer comprising at least two different monomers in polymerized form, in which the elastomer and the non-elastic copolymer are present in the elastomer composition in a ratio in weight 50:50 to 75:25, and at least one formulation of organic peroxides to provide a mixture, wherein the elastomer is saturated or unsaturated, the polymer is saturated or unsaturated, and said polymer does not comprise chlorinated or chlorosulfonated polyethylene; and wherein the formulation of organic peroxides comprises i) at least one organic peroxide, ii) at least one unit chosen from higher bis, tri and polyimelimides, and higher bis, tri and polycitraconimides, and iii) at least one sulfur accelerator; B) curing of said mixture in the presence of oxygen.
    [0002]
    Process according to claim 1, characterized in that the elastomer consists of a saturated ethylene-propylene terpolymer.
    [0003]
    Process according to claim 1, characterized in that the non-elastic copolymer is unsaturated poly (ethylenepropylene).
    [0004]
    Process according to claim 1, characterized by the fact that at least one organic peroxide is selected from the group consisting of dialkyl peroxides, diperoxicetals, monoperoxycarbonates, cyclic ketone peroxides, diacyl peroxides, organosulfonyl peroxides, peroxyesters and peroxydicarbonates.
    [0005]
    Process according to claim 1, characterized in that the elastomer consists of saturated ethylene-propylene terpolymer, the non-elastic copolymer is unsaturated poly (ethylenepropylene), and the unit is chosen from superior bis, tri and polyimaleides, and bis , tri and superior polycitraconimides.
    [0006]
    Cured elastomer composition, characterized by the fact that it is prepared by the process according to claim 1.
    [0007]
    Composition of elastomers curable in the presence of oxygen, characterized by the fact that said composition comprises: A) at least one elastomer comprising ethylene-propylene terpolymer which is saturated or unsaturated; B) at least one non-elastic copolymer comprising at least two different monomers in the polymerized form and which is saturated or unsaturated; C) at least one organic peroxide; D) at least one compound chosen from higher bis, tri and polymalimides, and higher bis, tri and polycitraconimides; and E) at least one sulfur accelerator; wherein the at least one polymer does not comprise chlorinated polyethylene or chlorosulfonated polyethylene;wherein the elastomer, and the inelastic copolymer, are present in the elastomer composition in a weight ratio of 50:50 to 75:25; such that said elastomer composition cross-links in the presence of oxygen.
    [0008]
    Composition according to claim 7, characterized in that the at least one organic peroxide is selected from dialkyl peroxides, diperoxicetals, monoperoxycarbonates, cyclic ketone peroxides, diacyl peroxides, organosulfonyl peroxides, peroxyesters and peroxydicarbonates.
    [0009]
    Composition according to claim 7, characterized in that the elastomer consists of saturated ethylene-propylene terpolymer and the at least one non-elastic copolymer is unsaturated poly (ethylenepropylene).
    [0010]
    Method for the manufacture of an article, characterized by the fact that it comprises a curable elastomer composition in the presence of oxygen, said elastomer composition comprising: A) at least one elastomer comprising ethylene-propylene terpolymer which is saturated or unsaturated; B) at least one non-elastic copolymer comprising at least two different monomers in the polymerized form and which is saturated or unsaturated; C) at least one organic peroxide; D) at least one compound chosen from superior bis, tri and polymalimides, and superior bis, tri epolicitraconimides; and E) at least one sulfur accelerator; wherein the at least one polymer does not comprise chlorinated polyethylene or chlorosulfonated polyethylene; wherein the at least one polymer does not comprise chlorinated polyethylene or chlorosulfonated polyethylene; wherein the elastomer and the inelastic copolymer are present in the elastomer composition in a weight ratio of 50:50 to 75:25; such that said elastomer composition cross-links in the presence of oxygen; said method comprising the steps of: - extruding said elastomer composition in the presence of hot air to form an uncured preformed article; - curing of said uncured preformed article.
    [0011]
    Method according to claim 10, characterized in that the curing of said extruded preform comprises curing using a microwave or a steam autoclave.
    [0012]
    Method according to claim 10, characterized in that the extrusion and curing of the elastomer composition is carried out continuously.
    [0013]
    Method according to claim 10, characterized in that the extrusion and curing of the elastomer composition is carried out continuously in a hot air tunnel.
    [0014]
    Method according to claim 10, characterized in that said article is a seal, a hose, or a gasket.
    [0015]
    Process to reduce molding fouling in the presence of oxygen during the manufacture of elastomeric articles, characterized by the fact that it comprises: A) the supply of an uncured elastomer composition in a mold, wherein the uncured elastomer composition comprises saturated ethylene-propylene terpolymer, at least one unsaturated non-elastic copolymer which is poly (ethylene propylene), in which the elastomer and the inelastic copolymer are present in the elastomer composition in a weight ratio of 50:50 to 75:25, at least one formulation of organic peroxides, wherein said at least one formulation of organic peroxides comprises i) at least one organic peroxide, ii) at least one unit chosen from superior bis, tri and polymaleimides, superior bis, tri and polycitraconimides, and p-phenylenediamines-based antiozones, and iii) at least one sulfur accelerator; B) curing the elastomer composition to form an elastomeric article; and C) releasing the cured elastomeric article from the mold.
    [0016]
    Process according to claim 15, characterized in that the at least one organic peroxide is selected from the group consisting of dialkyl peroxides, diperoxicetals, monoperoxycarbonates, cyclic ketone peroxides, dialkyl peroxides, organosulfonyl peroxides, peroxyesters and peroxydicarbonates.
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    同族专利:
    公开号 | 公开日
    RU2669844C2|2018-10-16|
    RU2015143433A|2017-04-26|
    BR112015022755B8|2020-08-04|
    MX2015012396A|2016-02-03|
    JP6484604B2|2019-03-13|
    JP2018119150A|2018-08-02|
    CN105189619A|2015-12-23|
    TW201434905A|2014-09-16|
    EP2970605A1|2016-01-20|
    EP2970605A4|2016-10-26|
    RU2015143433A3|2018-03-30|
    JP6533843B2|2019-06-19|
    WO2014158665A1|2014-10-02|
    AR095446A1|2015-10-14|
    JP2016518471A|2016-06-23|
    EP2970605B1|2021-12-01|
    CA2904590C|2019-08-06|
    CA2904590A1|2014-10-02|
    US9644089B2|2017-05-09|
    TWI618738B|2018-03-21|
    BR112015022755A2|2017-07-18|
    CN105189619B|2017-08-25|
    US20160017135A1|2016-01-21|
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    法律状态:
    2019-12-10| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|
    2020-05-12| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|
    2020-07-21| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 28/02/2014, OBSERVADAS AS CONDICOES LEGAIS. |
    2020-08-04| B16C| Correction of notification of the grant [chapter 16.3 patent gazette]|Free format text: REF. RPI 2585 DE 21/07/2020 QUANTO AO TITULO. |
    优先权:
    申请号 | 申请日 | 专利标题
    US201361782055P| true| 2013-03-14|2013-03-14|
    US61/782,055|2013-03-14|
    PCT/US2014/019194|WO2014158665A1|2013-03-14|2014-02-28|Methods for crosslinking polymer compositions in the presence of atmospheric oxygen|
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