Description

Fluoroelastomer curable composition

Cross-reference to Related Applications

[0001] This application claims priority to U.S. provisional application No.

62/629505 filed on February 12, 2018 and to European application No. 181901 15.8 filed on August 22, 2018, the whole content of each of these applications being incorporated herein by reference for all purposes.

Technical Field

[0002] The invention pertains to certain fluoroelastomer compositions having

ability to adhere upon curing to various substrates, to a process for their manufacture, to a method for fabricating shaped articles comprising curing the said fluoroelastomer compositions, to cured articles therefrom, and to assemblies including a substrate and said cured articles.

Background Art

[0003] Vulcanized (per)fluoroelastomers are materials with excellent heat- resistance and chemical-resistance characteristics, which are generally used in the manufacture of sealing articles such as oil seals, gaskets, shaft seals and O-rings in which the leak-tightness, the mechanical properties and the resistance to substances such as mineral oils, hydraulic fluids, solvents or chemical agents of diverse nature must be ensured over a wide range of working temperatures, from low to high temperatures, and wherein materials might be called to comply with severe requirements in terms of purity, plasma resistance and particles release.

[0004] In applications where the sealing part has to withstand mechanical forces, for example as a component of a part of a motor vehicle or for safety reasons, for example, as a component of a storage device for fuels, the fluoroelastomer component may be secured to a another part, which may be a metal part or a plastic part, particularly silicone, polycarbonate, polyester, or polyamide, resulting in a multi-material component

possessing performance that combines the best attributes of both constituents. Such assemblies are required to possess strong bonding among each other: it is not an easy task to get robust adhesion of cured (per)fluoroelastomer to metals or plastics, because of their low surface energy and lack of functional groups.

[0005] Several attempts have been already exemplified in the past for addressing the challenge of improving adhesion between fluororubbers and different substrates.

[0006] For instance, U.S. Pat. No. 5,656,121 describes that composite materials of fluoropolymers with other thermoplastic resins can be prepared by using a coating containing low molecular weight diamine compound to create a strong bond between the components. However, for economical reasons it may be desirable for the composite material to be formed directly by combining the elastic and the rigid components without requiring adhesives or bonding additives like tie-layers and primers to avoid additional processing steps and material costs.

[0007] Still, in U.S. Pat. No. 6,162,385 composite materials with strong and direct bonds between fluoroelastomer and polyamide polymer are described, whereas the polyamide is selected in a manner to possess high

concentration of amine end groups, and the fluoroelastomer is ionically cured while adhering thereto.

[0008] Yet in this domain, EP2714388 is directed to a composite material

comprising a first component directly bonded to a second component, the first component comprising a peroxide cured fluoroelastomer having a temperature reflection TR-10 of -19 C or lower as measured according to ASTM D 1329 and the second component comprising a polyamide resin, this composite material possessing heat stable bonds between the fluoroelastomer and the polyamide.

[0009] Nevertheless, none of these approaches actually provides for a solution based on a (per)fluoroelastomer base compound having ability to adhere to a variety of substrates, with no peculiar pre-treatment or modification of the said substrate, and which can be easily processed in e.g. 2K molding processing machineries, with optimum performances. [0010] JP 2017/071686 relates to a perfluororubber molding including a body made from a perfluororubber including powder of the aromatic heat- resistant resin blended therein, and a coating of an aromatic heat-resistant resin on at least a part of the surface of the molding. The heat-resistant resin may be an aromatic polyimide.

[0011] US7323515 relates to a sealing composition which comprises a cross- linkable fluoroelastomer, a crosslinking agent and a reinforcing polyimide resin powder.

[0012] WO 2006/010651 is directed to an aromatic polyimide composition

comprising an aromatic polyamide-imide and an amount of 0.5 to 30 % wt of a fluoroelastomer, possessing improved flexibility during molding process, suitable for molding parts having undercuts or complex geometry.

Summary of invention

[0013] The Applicant has now found that certain compositions comprising a

(per)fluoroelastomer, a cross-linking system, and a well-defined amount of at least one polyamideimide can solve above mentioned problems and are particularly effective in enabling curing to deliver outstanding adhesion to a variety of substrates, while maintaining all the advantageous mechanical and sealing properties of (per)fluoroelastomers.

[0014] The invention hence pertains to a composition [composition (C)]

comprising:

- at least one (per)fluoroelastomer [fluoroelastomer (A)];

- at least one cross-linking system; and

- at least one aromatic polyamide-imide polymer [polymer (PAI)], said polymer (PAI) being present in an amount of at least 0.5 phr, and at most 30.0 phr, with respect to the fluoroelastomer (A).

[0015] For the purposes of this invention, the term“(per)fluoroelastomer”

[fluoroelastomer (A)] is intended to designate a fluoropolymer resin serving as a base constituent for obtaining a true elastomer, said fluoropolymer resin comprising more than 10 % wt, preferably more than 30 % wt, of recurring units derived from at least one ethylenically unsaturated monomer comprising at least one fluorine atom (hereafter, (per)fluorinated monomer) and, optionally, recurring units derived from at least one ethylenically unsaturated monomer free from fluorine atom (hereafter, hydrogenated monomer) .

[0016] True elastomers are defined by the ASTM, Special Technical Bulletin,

No. 184 standard as materials capable of being stretched, at room temperature, to twice their intrinsic length and which, once they have been released after holding them under tension for 5 minutes, return to within 10 % of their initial length in the same time.

[0017] Generally fluoroelastomer (A) comprises recurring units derived from at least one (per)fluorinated monomer, wherein said (per)fluorinated monomer is generally selected from the group consisting of:

- C2-C8 fluoro- and/or perfluoroolefins, such as tetrafluoroethylene (TFE), hexafluoropropene (HFP), pentafluoropropylene, and hexafluoroisobutylene;

- C2-C8 hydrogenated monofluoroolefins, such as vinyl fluoride;

1 ,2-difluoroethylene, vinylidene fluoride (VDF) and trifluoroethylene (TrFE);

- (per)fluoroalkylethylenes complying with formula CFh=CFI-R _f o, in which Rro is a C1-C6 (per)fluoroalkyl or a C1-C6 (per)fluorooxyalkyl having one or more ether groups ;

- chloro- and/or bromo- and/or iodo-C2-C6 fluoroolefins, like chlorotrifluoroethylene (CTFE);

- fluoroalkylvinylethers complying with formula CF ₂ =CFOR _fi in which R _fi is a C ₁ -C6 fluoro- or perfluoroalkyl, e.g. -CF ₃ , -C ₂ F ₅ , -C3F ₇ ;

- hydrofluoroalkylvinylethers complying with formula CFl ₂ =CFOR _fi in which R _fi is a C ₁ -C6 fluoro- or perfluoroalkyl, e.g. -CF ₃ , -C ₂ F ₅ , -C ₃ F ₇ ;

- fluoro-oxyalkylvinylethers complying with formula CF ₂ =CFOXo, in which Xo is a C ₁ -C ₁₂ oxyalkyl, or a C ₁ -C ₁₂ (per)fluorooxyalkyl having one or more ether groups; in particular (per)fluoro-methoxy-vinylethers complying with formula CF ₂ =CF0CF ₂ 0R _f2 in which R _f2 is a C ₁ -C6 fluoro- or perfluoroalkyl, e.g. -CF ₃ , -C ₂ F ₅ , -C ₃ F ₇ or a C ₁ -C6 (per)fluorooxyalkyl having one or more ether groups, like -C ₂ Fs-0-CF ₃ ; - functional fluoro-alkylvinylethers complying with formula CF2=CFOYo, in which Yo is a C1-C12 alkyl or (per)fluoroalkyl, or a C1-C12 oxyalkyl or a C1-C12 (per)fluorooxyalkyl, said Yo group comprising a carboxylic or sulfonic acid group, in its acid, acid halide or salt form;

- (per)fluorodioxoles, of formula :

wherein each of Rf3 _, Rf4 _, Rts _, Rf6, equal to or different from each other, is independently a fluorine atom, a C1-C6 fluoro- or per(halo)fluoroalkyl, optionally comprising one or more oxygen atom, e.g. -CF3, -C2F ₅ , - C3F7, -OCFs, -OCF2CF2OCF3.

[0018] Examples of hydrogenated monomers are notably hydrogenated alpha- olefins, including ethylene, propylene, 1 -butene, diene monomers, styrene monomers, alpha-olefins being typically used.

[0019] Fluoroelastomers (A) are in general amorphous products or products

having a low degree of crystallinity (crystalline phase less than 20 % by volume) and a glass transition temperature (T _g ) below room temperature.

In most cases, the fluoroelastomer (A) has advantageously a T _g below 10° C, preferably below 5°C, more preferably 0°C.

[0020] The fluoroelastomer (A) is preferably selected among:

(1) VDF-based copolymers, in which VDF is copolymerized with at least one additional comonomer selected from the group consisting of :

(a) C2-C8 perfluoroolefins , such as tetrafluoroethylene (TFE),

hexafluoropropylene (FIFP);

(b) hydrogen-containing C2-C8 olefins, such as vinyl fluoride (VF), trifluoroethylene (TrFE), hexafluoroisobutene (HFIB), perfluoroalkyl ethylenes of formula CH2 = CH-Rf, wherein Rf is a C1-C6 perfluoroalkyl group;

(c) C2-C8 fluoroolefins comprising at least one of iodine, chlorine and bromine, such as chlorotrifluoroethylene (CTFE);

(d) (per)fluoroalkylvinylethers (PAVE) of formula CF2 = CFORf, wherein Rf is a Ci-C ₆ (per)fluoroalkyl group, preferably CF3, C2F5, C3F7;

(e) (per)fluoro-oxy-alkylvinylethers of formula CF2 = CFOX, wherein X is a C1-C12 ((per)fluoro)-oxyalkyl comprising catenary oxygen atoms, e.g. the perfluoro-2-propoxypropyl group;

(f) (per)fluorodioxoles having formula :

wherein each of Rf3, Rf4, Rts, Rf6, equal to or different from each other, is independently selected from the group consisting of fluorine atom and C1- C ₆ (per)fluoroalkyl groups, optionally comprising one or more than one oxygen atom, such as notably -CF3, -C2F5, -C3F7, -OCF3, -OCF2CF2OCF3; preferably, perfluorodioxoles;

(g) (per)fluoro-methoxy-vinylethers (MOVE, hereinafter) having formula: CF ₂ =CFOCF ₂ ORf2

wherein Rf2 is selected from the group consisting of C1-C6 (per)fluoroalkyls; C ₅ -C6 cyclic (per)fluoroalkyls; and C2-C6 (per)fluorooxyalkyls, comprising at least one catenary oxygen atom; Rf2 is preferably -CF2CF3 (MOVE1); - CF2CF2OCF3 (MOVE2); or -CF ₃ (MOVE3);

(h) C2-C8 non-fluorinated olefins (Ol), for example ethylene and propylene; and

(2) TFE-based copolymers, in which TFE is copolymerized with at least one additional comonomer selected from the group consisting of (c), (d), (e), (g), (h) and (i) as above detailed .

[0021] Optionally, fluoroelastomer (A) of the present invention may also

comprises recurring units derived from a bis-olefin [bis-olefin (OF)] having

general formula wherein R1, R2, R3,

R ₄ , Rs and R6, equal or different from each other, are FI or C1-C ₅ alkyl; Z is a linear or branched C1-C18 (hydro)carbon radical (including alkylene or cycloalkylene radical), optionally containing oxygen atoms, preferably at least partially fluorinated, or a (per)fluoro(poly)oxyalkylene radical comprising one or more catenary ethereal bonds.

[0022] The bis-olefin (OF) is preferably selected from the group consisting of those complying with formulae (OF-1), (OF-2) and (OF-3) :

(OF-1)

wherein j is an integer between 2 and 10, preferably between 4 and 8, and R1 , R2, R3, R4, equal or different from each other, are H, F or Ci-s alkyl or (per)fluoroalkyl group;

(OF-2)

wherein each of A, equal or different from each other and at each occurrence, is independently selected from F, Cl, and H; each of B, equal or different from each other and at each occurrence, is independently selected from F, Cl, H and ORB, wherein RB is a branched or straight chain alkyl radical which can be partially, substantially or completely fluorinated or chlorinated; E is a divalent group having 2 to 10 carbon atom, optionally fluorinated, which may be inserted with ether linkages;

preferably E is a -(CF2) _m - group, with m being an integer from 3 to 5; a preferred bis-olefin of (OF-2) type is F2C=CF-0-(CF2)5-0-CF=CF2.

(OF-3)

wherein E, A and B have the same meaning as above defined; R5, R6 R7, equal or different from each other, are H, F or Ci-5 alkyl or

(per)fluoroalkyl group.

[0023] Among specific compositions of fluoroelastomers (A) suitable for the

purpose of the invention, mention can be made of fluoroelastomers having the following compositions (in mol %) :

(i) vinylidene fluoride (VDF) 35-85 %, hexafluoropropene (HFP) IQ-

45 %, tetrafluoroethylene (TFE) 0-30 %, perfluoroalkyl vinyl ethers (PAVE) 0-15 %, bis-olefin (OF) 0-5 %;

(ii) vinylidene fluoride (VDF) 50-80 %, perfluoroalkyl vinyl ethers (PAVE) 5-50 %, tetrafluoroethylene (TFE) 0-20 %, bis-olefin (OF) 0-5 %;

(iii) vinylidene fluoride (VDF) 20-30 %, C2-C8 non-fluorinated olefins (Ol) 10-30 %, hexafluoropropene (HFP) and/or perfluoroalkyl vinyl ethers (PAVE) 18-27 %, tetrafluoroethylene (TFE) 10-30 %, bis-olefin (OF) 0-5 %;

(iv) tetrafluoroethylene (TFE) 50-80 %, perfluoroalkyl vinyl ethers (PAVE) 20-50 %, bis-olefin (OF) 0-5 %;

(v) tetrafluoroethylene (TFE) 45-65 %, C2-C8 non-fluorinated olefins (Ol) 20-55 %, vinylidene fluoride 0-30 %, bis-olefin (OF) 0-5 %;

(vi) tetrafluoroethylene (TFE) 32-60 % mol %, C2-C8 non-fluorinated olefins (Ol) 10-40 %, perfluoroalkyl vinyl ethers (PAVE) 20-40 %, fluorovinyl ethers (MOVE) 0-30 %, bis-olefin (OF) 0-5 %;

(vii) tetrafluoroethylene (TFE) 33-75 %, perfluoroalkyl vinyl ethers (PAVE) 15-45 %, vinylidene fluoride (VDF) 5-30 %, hexafluoropropene HFP 0-

30 %, bis-olefin (OF) 0-5 %;

(viii) vinylidene fluoride (VDF) 35-85 %, fluorovinyl ethers (MOVE) 5- 40 %, perfluoroalkyl vinyl ethers (PAVE) 0-30 %, tetrafluoroethylene (TFE) 0-40 %, hexafluoropropene (HFP) 0-30 %, bis-olefin (OF) 0-5 %;

(ix) tetrafluoroethylene (TFE) 20-70 %, fluorovinyl ethers (MOVE) 30- 80 %, perfluoroalkyl vinyl ethers (PAVE) 0-50 %, bis-olefin (OF) 0-5 %.

[0024] The fluoroelastomer (A) can be prepared by any known method, such as emulsion or micro-emulsion polymerization, suspension or micro- suspension polymerization, bulk polymerization and solution

polymerization. [0025] According to certain preferred embodiments of the invention, the

fluoroelastomer (A) comprises cure sites; the selection of cure sites is not particularly critical, provided that they ensure adequate reactive in curing.

[0026] The fluoroelastomer (A) can comprise said cure sites either as pendant groups bonded to certain recurring units or as end groups of the polymer chain.

[0027] Among cure-site containing recurring units, mention can be notably made of :

(CSM-1) halogen (chlorine, iodine or bromine, preferably iodine or bromine) containing monomers of formula:

wherein each of Aw, equal to or different from each other and at each occurrence, is independently selected from F, Cl, and H; B _HΪ is any of F,

Cl, H and OR ^Hf B, wherein R ^Hf B is a branched or straight chain alkyl radical which can be partially, substantially or completely fluorinated or

chlorinated; each of W ^Hf equal to or different from each other and at each occurrence, is independently a covalent bond or an oxygen atom; EHI is a divalent group having 2 to 10 carbon atom, optionally fluorinated; R _hif is a branched or straight chain alkyl radical, which can be partially,

substantially or completely fluorinated, which may be inserted with ether linkages; preferably E is a -(CF2) _m - group, with m being an integer from 3 to 5; and XHI is a halogen atom selected from the group consisting of Chlorine, Iodine and Bromine, preferably selected from the group consisting of Iodine and Bromine;

(CSM-2) ethylenically unsaturated compounds comprising cyanide groups, possibly fluorinated.

[0028] Among cure-site containing monomers of type (CSM1), preferred

monomers are those selected from the group consisting of:

(CSM1-A) iodine-containing perfluorovinylethers of formula:

with m being an integer from 0 to 5 and n being an integer from 0 to 3, with the provisio that at least one of m and n is different from 0, and R _f , being F or CF3; (as notably described in patents US 4745165 (AUSIMONT SPA ) 17/05/1988 , US 4564662 (MINNESOTA MINING ) 14/01/1986 and EP 199138 A (DAI KIN IND LTD ) 29/10/1986 ); and

(CSM-1 B) iodine-containing ethylenically unsaturated compounds of formula:

CX ¹ X ² =CX ³ -(CF ₂ CF ₂ ) _p -I

wherein each of X ¹ , X ² and X ³ , equal to or different from each other, are independently H or F; and p is an integer from 1 to 5; among these compounds, mention can be made of CH ₂ =CHCF ₂ CF ₂ I,

l(CF ₂ CF ₂ ) ₂ CH=CH ₂ , ICF ₂ CF ₂ CF=CH _2J l(CF ₂ CF ₂ ) ₂ CF=CH ₂ ;

(CSM-1C) iodine-containing ethylenically unsaturated compounds of formula:

CHR=CH-Z-CH ₂ CHR-I

wherein R is H or CH3, Z is a C ₁ -C ₁₈ (per)fluoroalkylene radical, linear or branched, optionally containing one or more ether oxygen atoms, or a (per)fluoropolyoxyalkylene radical; among these compounds, mention can be made of CH ₂ =CH-(CF ₂ ) ₄ CH ₂ CH ₂ I, CH ₂ =CH-(CF ₂ ) ₆ CH ₂ CH ₂ I, CH ₂ =CH- (CF ₂ ) _S CH ₂ CH ₂ I, CH ₂ =CH-(CF ₂ ) ₂ CH ₂ CH ₂ I;

(CSM-1 D) bromo and/or iodo alpha-olefins containing from 2 to 10 carbon atoms such as bromotrifluoroethylene or bromotetrafluorobutene described, for example, in US 4035565 (DU PONT ) 12/07/1977 or other compounds bromo and/or iodo alpha-olefins disclosed in US 4694045 (DU PONT ) 15/09/1987 .

[0029] Among cure-site containing monomers of type (CSM2), preferred

monomers are those selected from the group consisting of:

(CSM2-A) perfluorovinyl ethers containing cyanide groups of formula CF ₂ =CF-(0CF ₂ CFX ^CN ) _m -0-(CF ₂ ) _n -CN, with X ^CN being F or CF ₃ , m being 0, 1 , 2, 3 or 4; n being an integer from 1 to 12;

(CSM2-B) perfluorovinyl ethers containing cyanide groups of formula CF ₂ =CF-(0CF ₂ CFX ^CN ) _m’ -0-CF2— CF(CF ₃ )-CN, with X ^CN being F or CF ₃ , m’ being 0, 1 , 2, 3 or 4.

Specific examples of cure-site containing monomers of type CSM2-A and CSM2-B suitable to the purposes of the present invention are notably those described in patents US 4281092 (DU PONT ) 28/07/1981 , US 4281092 (DU PONT ) 28/07/1981 , US 5447993 (DU PONT ) 5/09/1995 and US 5789489 (DU PONT ) 4/08/1998 .

[0030] Preferably, fluoroelastomer (A) of the invention comprises at least one of chlorine, iodine and bromine cure sites (more preferably iodine and/or bromine), in an amount such that the chloride, iodine and bromine content in the fluoroelastomer (A) is of 0.001 to 10% wt, with respect to the total weight of fluoroeastomer (A). Among these, iodine cure sites are those selected for maximizing curing rate, so that fluoroelastomers (A)

comprising iodine cure-sites are preferred.

[0031] According to this embodiment, for ensuring acceptable reactivity it is

generally understood that iodine and/or bromine are preferred and that the content of iodine and/or bromine in the fluoroelastomer (A) should be of at least 0.05 % wt, preferably of at least 0.1 % weight, more preferably of at least 0.15 % weight, with respect to the total weight of fluoroelastomer (A).

[0032] On the other side, amounts of iodine and/or bromine not exceeding

preferably 7 % wt, more specifically not exceeding 5 % wt, or even not exceeding 4 % wt, with respect to the total weight of fluoroelastomer (A), are those generally selected for avoiding side reactions and/or detrimental effects on thermal stability.

[0033] These iodine or bromine cure sites of these preferred embodiments of the invention might be comprised as pending groups bound to the backbone of the fluoroelastomer (A) polymer chain (by means of incorporation in the fluoroelastomer (A) chain of recurring units derived from monomers of (CSM-1) type, as above described, and preferably of monomers of (CSM- 1A) to (CSM1-D), as above detailed) or might be comprised as terminal groups of said polymer chain.

[0034] According to a first embodiment, the iodine and/or bromine cure sites are comprised as pending groups bound to the backbone of the fluoroelastomer polymer chain. The fluoroelastomer according to this embodiment generally comprises recurring units derived from iodine or bromine containing monomers (CSM-1) in amounts of 0.05 to 5 mol per 100 mol of all other recurring units of the fluoroelastomer (A), so as to advantageously ensure above mentioned iodine and/or bromine weight content.

[0035] According to a second preferred embodiment, the iodine and/or bromine cure sites are comprised as terminal groups of the fluoroelastomer (A) polymer chain; the fluoroelastomer according to this embodiment is generally obtained by addition to the polymerization medium during fluoroelastomer manufacture of anyone of:

- iodinated and/or brominated chain-transfer agent(s); suitable chain-chain transfer agents are typically those of formula R _f (l) _x (Br) _y , in which R _f is a (per)fluoroalkyl or a (per)fluorochloroalkyl containing from 1 to 8 carbon atoms, while x and y are integers between 0 and 2, with 1 < x+y < 2 (see, for example, patents US 4243770 (DAI KIN IND LTD ) 6/01/1981 and US 4943622 (NIPPON MEKTRON KK ) 24/07/1990 ); and

- alkali metal or alkaline-earth metal iodides and/or bromides, such as described notably in patent US 5173553 (AUSIMONT SRL) 22/12/1992 .

[0036] The polymer (PAI)

[0037] To the purpose of the present invention, the term“aromatic polyamide- imide polymer [polymer (PAI)]” is intended to denote any polymer comprising more than 50% by moles of recurring units comprising at least one aromatic ring, at least one imide group, as such and/or in its amic acid form, and at least one amide group which is not included in the amic acid form of an imide group [recurring units (RPAI)].

[0038] The recurring units (RPAI) are advantageously selected from the group consisting of units of any of formulae (Rp _Ai -a) and (Rp _Ai -b):

(amic acid form)

(imide form)

wherein:

- Ar is a trivalent aromatic group; typically Ar is selected from the group consisting of the following

structures:

and corresponding optionally substituted structures, with X being -0-, - C(O)-, -CH2-, -C(CF3)2-, -(CF2) _n -, with n being an integer from 1 to 5;

- R is a divalent aromatic group; typically R is selected from the group consisting of the following structures:

and corresponding optionally substituted structures, with Y being -0-, -S- , -SO2-, -CH2-, -C(0)-, -C(CF3)2-, -(CF2) _n , n being an integer from 0 to 5.

[0039] Preferably, the polymer (PAI) comprises more than 50% by moles of

recurring units (RPAI) comprising an imide group wherein the imide group is present as such, like in recurring units (Rp _Ai -a), and/or in its amic acid form, like in recurring units (Rp _Ai -b), with respect to the total number of moles of recurring units of polymer (PAI). [0040] Recurring units (R _PAI ) are preferably selected from recurring units (I), (m) and (n), in their amide-imide (a) or amide-amic acid (b) forms:

wherein the attachment of the two amide groups to the aromatic ring as shown in (l-b) will be understood to represent the 1 ,3 and the 1 ,4 polyamide-amic acid configurations;

wherein the attachment of the two amide groups to the aromatic ring as shown in (m-b) will be understood to represent the 1 ,3 and the 1 ,4 polyamide-amic acid configurations; and

(amide-imide form)

(amide-amic acid form) wherein the attachment of the two amide groups to the aromatic ring as shown in (n-b) will be understood to represent the 1 ,3 and the 1 ,4 polyamide-amic acid configurations.

[0041] Very preferably, the polymer (PAI) comprises more than 90% by moles of recurring units (RPAI). Still more preferably, it contains no recurring unit other than recurring units (RPAI). Polymers (PAI) are notably commercialized by Solvay Specialty Polymers USA, L.L.C. under the trademark name TORLON ^® .

[0042] The composition (C) comprises said polymer (PAI) in an amount of at least 0.5 phr, preferably at least 1.0 phr, more preferably at least 2.0 phr, and at most 30.0 phr, preferably at most 25.0 phr, more preferably at most 18.0 phr, with respect to the fluoroelastomer (A).

[0043] The cross-linking system

[0044] The composition (C) comprises at least one cross-linking system, which is able to promote the curing of the fluoroelastomer (A).

[0045] According to certain embodiments, the said at least one cross-linking

system is a peroxide-based cross-linking system comprising at least one organic peroxide [peroxide (O)] and at least one one polyunsaturated compound [compound (U)].

[0046] The composition (C) according to this embodiment hence comprises at least an organic peroxide [peroxide (O)]; the choice of the said peroxide (O) is not particularly critical provided that the same is capable of generating radicals with the assistance of a transition metal catalyst.

Among most commonly used peroxides, mention can be made of:

- di(alkyl/alryl) peroxides, including for instance di-tert-butyl peroxide, 2,5- dimethyl-2,5-bis(tert-butylperoxy)hexane, di(t- butylperoxyisopropyl)benzene, dicumyl peroxide;

- diacyl peroxides, including dibenzoyl peroxide, disuccinic acid peroxide, di(4-methylbenzoyl)peroxide, di(2,4-dichlorobenzoyl)peroxide, dilauroyl peroxide, decanoyl peroxide;

- percarboxylic acids and esters, including di-tert-butyl perbenzoate, t- butylperoxy-2-ethylhexanoate, 1 ,1 ,3,3-tetramethylethylbutyl peroxy-2- ethylhexanoate, 2,5-dimethyl-2,5-di(2-ethylhexanoylperoxy)hexane;

- peroxycarbonates including notably di(4-t- butylcyclohexyl)peroxydicarbonate, di(2-phenoxyethyl)peroxydicarbonate, bis[1 ,3-dimethyl-3-(tert-butylperoxy)butyl] carbonate, t- hexylperoxyisoproprylcarbonate, t-butylperoxyisopropylcarbonate,

- perketals such as 1 , 1-bis(tert-butylperoxy)cyclohexane and 2, 2- bis(tertbutylperoxy)butane; - ketone peroxides such as cyclohexanone peroxide and acetyl acetone peroxide;

- organic hydroperoxides such as cumene hydroperoxide, tert-butyl hydroperoxide, methylethylketone peroxide (otherwise referred to as 2-[(2- hydroperoxybutan-2-yl)peroxy]butane-2-peroxol) and pinane

hydroperoxide;

- oil-soluble azo initiators such as 2, 2'-azobis (4-methoxy-2. 4-dimethyl valeronitrile), 2, 2'-azobis (2.4-dimethyl valeronitrile), 2,2'- azobis(isobutyronitrile), 2, 2'-azobis(2-cyano-2-butane), dimethyl-2, 2'- azobisdimethyli sobutyrate, dimethyl-2, 2'-azobis(2-methylpropionate), 2,2'- azobis(2-methylbutyronitrile), 1 ,1'-azobis(cyclohexane-l-carbonitrile), 2, 2'- azobis[N-(2-propenyl)-2-methylpropionamide], 1 -[(1 -cyano-1 -methyl ethyl)azo]formamide, 2, 2'-azobis(N-cyclohexy1 -2-methylpropionamide), 2,2'-azobis(i sobutyronitrile), 2,2'-azobis(2-cyano-2-butane), dimethyl-2, 2'- azobisdimethylisobutyrate, 1 , 1 '-azobis(cyclohexanecarbonitrile), 2-(t- butylazo)-2-cyanopropane, 2,2'-azobis[2-methyl-N-(1 , 1)- bis(hydroxymethyl)-2-hydroxyethyl]propionamide, 2, 2'-azobis[2-methyl-N- hydroxyethyl]-proprionamide, 2, 2'-azobis(N, N'- dimethyleneisobutyramine), 2, 2'-azobis(2-methyl-N-[1 ,1- bis(hydroxymethyl)-2-hydroxyethyl] propionamide), 2,2'-azobis(2-methyl- N-[1 ,1-bis(hydroxymethyl) ethyl] proprionamide), 2, 2'-azobis[2-5 methyl- N-(2-hydroxyethyl) propionamide], 2,2'-azobis(isobutyramide) dihydrate, 2,2'-azobis(2, 2, 4-trimethylpentane), 2, 2'-azobis(2-methylpropane).

[0047] Other suitable peroxide systems are those described, notably, in patent applications EP 136596 A (MONTEDISON SPA ) 10/04/1985 and EP 410351 A (AUSIMONT SRL ) 30/01/1991 , whose content is hereby incorporated by reference.

[0048] Choice of the most appropriate peroxide depending upon curing conditions (time, temperature) will be done by one of ordinary skills in the art considering notably ten-hours half time temperature of the peroxide (O).

[0049] The amount of peroxide (O) in the composition (C) of this embodiment is generally of 0.1 to 15 phr, preferably of 0.2 to 12 phr, more preferably of 1.0 to 7.0 phr, relative to 100 weight parts of fluoroelastomer (A). [0050] As said, the composition (C) of this embodiment comprises at least one polyunsaturated compound or compound (U). The expression“

polyunsaturated compound” is hereby intended to designate a compound comprising more than one carbon-carbon unsaturation.

[0051] The composition (C) may comprise one or more than one compound (U), as above detailed.

[0052] Compounds (U) may be selected from compounds comprising two carbon- carbon unsaturations, compounds comprising three carbon-carbon unsaturations and compounds comprising four or more than four carbon- carbon unsaturations.

[0053] Among compounds (U) comprising two carbon-carbon unsaturations, mention can be made of bis-olefins [bis-olefin (OF)], as above detailed, preferably selected from those complying with any of formulae (OF-1 ), (OF-2) and (OF-3), as above detailed.

[0054] Among compounds (U) comprising three carbon-carbon unsaturations, mention can be made of:

- tri-substuituted cyanurate compounds of general formula:Among compounds (U) comprising three carbon-carbon unsaturations, mention can be made of:

- tri-substuituted cyanurate compounds of general formula:

wherein each of R _cy , equal to or different from each other and at each occurrence, is independently selected from FI or a group -R _rcy or-OR _rcy , with R _rcy being C1 -C5 alkyl, possibly comprising halogen(s), and each of J _cy , equal to or different from each other and at each occurrence, is independently selected from a bond or a divalent hydrocarbon group, optionally comprising heteroatoms;

tri-substuituted cyanurate compounds include notably preferred triallyl cyanurate, trivinyl cyanurate;

- tri-substuituted isocyanurate compounds of general formula:

wherein each of Risocy, equal to or different from each other and at each occurrence, is independently selected from H or a group -Rrisocy or-ORrisocy , with Rrisocy being C1-C5 alkyl, possibly comprising halogen(s), and each of Jisocy, equal to or different from each other and at each occurrence, is independently selected from a bond or a divalent hydrocarbon group, optionally comprising heteroatoms;

tri-substuituted isocyanurate compounds include notably preferred triallyl isocyanurate (otherwise referred to as“TAIC”), trivinyl isocyanurate, with TAIC being the most preferred;

- tri-substituted triazine compounds of general formula:

wherein each of R _az , equal to or different from each other and at each occurrence, is independently selected from H or a group -Rraz Or-OR _ra z , with R _raz being C1 -C5 alkyl, possibly comprising halogen(s), and each of J _az , equal to or different from each other and at each occurrence, is independently selected from a bond or a divalent hydrocarbon group, optionally comprising heteroatoms; tri-substituted triazine compounds

include notably compounds disclosed in EP 0860436 A (AUSIMONT SPA) 26/08/1998 and in WO 97/05122 (DU PONT) 13/02/1997 ;

- tri-substituted phosphite compounds of general formula:

wherein each of R _Ph , equal to or different from each other and at each occurrence, is independently selected from H or a group -R _rph or-OR _rph , with R _rph being C1 -C5 alkyl, possibly comprising halogen(s), and each of J _Ph , equal to or different from each other and at each occurrence, is independently selected from a bond or a divalent hydrocarbon group, optionally comprising heteroatoms; tri- substituted phosphite compounds

include notably preferred tri-allyl phosphite;

- tri-substituted alkyltrisiloxanes of general formula:

wherein each of R _s , equal to or different from each other and at each occurrence, is independently selected from H or a group -Rrsi or -ORrsi, with R _rSi being C1 -C5 alkyl, possibly comprising halogen(s), each of R’ _S i, equal to or different from each other and at each occurrence, is independently selected from C1 -C5 alkyl groups, possibly comprising halogen(s), and each of J _S i, equal to or different from each other and at each occurrence, is independently selected from a bond or a divalent hydrocarbon group, optionally comprising heteroatoms; tri- substituted alkyltrisiloxanes compounds include notably preferred 2,4,6- trivinyl methyltrisiloxane and 2,4,6-trivinyl ethyltrisiloxane;

- N,N-disubstituted acrylamide compounds of general formula:

wherein each of Ra _n , equal to or different from each other and at each occurrence, is independently selected from H or a group— Rran or— ORran, with R _ran being C1-C5 alkyl, possibly comprising halogen(s), and each of J _an , equal to or different from each other and at each occurrence, is independently selected from a bond or a divalent hydrocarbon group, optionally comprising heteroatoms; N,N-disubstituted acrylamide compounds include notably preferred N,N-diallylacrylamide.

[0055] Among compounds (U) comprising four or more carbon-carbon

unsaturations, mention can be made of tris(diallylamine)-s-triazine of

formula , hexa-allylphosphoramide,

N,N,N',N'-tetra-allyl terephthalamide, N,N,N',N'-tetra-allyl malonamide.

[0056] It is generally preferred for the compound (U) to be selected from the group consisting of (i) olefins (OF), as above detailed, in particular olefins of (OF-1) type; and (ii) tri-substuituted isocyanurate compounds, as above detailed, in particular TAIC.

[0057] The amount of the compound (U) ranges normally from 0.1 to 20 weight parts per 100 parts by weight (phr) of fluoroelastomer (A), preferably from 1 to 15 weight parts per 100 parts by weight of fluoroelastomer (A), more preferably from 1 to 10 weight parts per 100 parts by weight of

fluoroelastomer (A).

[0058] The composition (C) of this embodiment may further additionally comprise ingredients which maybe commonly used for the peroxide curing of fluoroelastomers; more specifically, composition (C) may generally further comprise

(a) one or more than one metallic basic compound, in amounts generally of from 0.5 to 15.0 phr, and preferably of from 1 to 10 phr, more preferably 1 to 5 phr, relative to 100 weight parts of fluoroelastomer (A); metallic basic compounds are generally selected from the group consisting of (j) oxides or hydroxides of divalent metals, for instance oxides or hydroxides of Mg, Zn, Ca or Pb, and (jj) metal salts of a weak acid, for instance Ba,

Na, K, Pb, Ca stearates, benzoates, carbonates, oxalates or phosphites;

(b) one or more than one acid acceptor which is not a metallic basic compound, in amounts generally of from 0.5 to 15.0 phr, and preferably of from 1 to 10.0 phr, more preferably 1 to 5 phr, relative to 100 weight parts of fluoroelastomer (A); these acid acceptors are generally selected from nitrogen-containing organic compounds, such as

1 ,8-bis(dimethylamino)naphthalene, octadecylamine, etc., as notably described in EP 708797 A (DU PONT ) 1/05/1996 .

[0059] According to other embodiments, the said at least one cross-linking

system is a ionic-based cross-linking system comprising at least one polyhydroxylated compound, at least one accelerant, and at least one basic metal oxide.

[0060] As said, the composition according to this second embodiment comprises at least one polyhydroxylated compounds. Aromatic or aliphatic

polyhydroxylated compounds, or derivatives thereof, may be used ;

examples thereof are described, notably, in EP 335705 A (MINNESOTA MINING) 4/10/1989 and US 4233427 (RHONE POULENC IND)

11/11/1980 . Among these, mention will be made in particular of dihydroxy, trihydroxy and tetrahydroxy benzenes, naphthalenes or anthracenes;

bisphenols of formula (B):

wherein:

- Z' is selected from the group consisting of bivalent C1-C13 alkyl or alkylidene group, C ₄ -Ci3 cycloaliphatic, C6-C13 aromatic or arylalkylenic groups, optionally substituted with at least one chlorine or fluorine atom; a thio (-S-), oxy (-0-), carbonyl (-C(O)-), sulphinyl (-S(O)-) and sulphonyl group (-SO2-);

- x is 0 or 1 ;

- u, equal to or different from each other, is independently at each occurrence an integer of at least 1 , preferably 1 or 2;

- and wherein the phenyl rings can be optionally substituted by one or more substituents selected from the group consisting of chlorine, fluorine, bromine; -CHO, Ci-Cs alkoxy groups, -COOR10 groups, wherein R10 is H or Ci-Cs alkyl, C6-Ci ₄ aryl, C ₄ -Ci2 cycloalkyl.

[0061] When Z' is a C 1 -Ci 3 divalent alkyl group, it can be for example methylene, ethylene, chloroethylene, fluoroethylene, difluoroethylene, 1 ,3-propylene, tetramethylene, chlorotetramethylene, fluorotetramethylene,

trifluorotetramethylene, 2-methyl-1 ,3-propylene, 2-methyl-1 ,2-propylene, pentamethylene, hexamethylene.

When Z' is a C1-C13 divalent alkylidene group, it can be for example ethylidene, dichloroethylidene, difluoroethylidene, propylidene,

isopropylidene, trifluoroisopropylidene, hexafluoroisopropylidene, butylidene, heptachlorobutylidene, heptafluorobutylidene, pentylidene, hexylidene, 1 ,1-cyclohexylidene.

When Z' is C ₄ -C 13 cycloaliphatic group, it can be for example 1 ,4- cyclohexylene, 2-chloro-1 ,4-cyclohexylene, 2-fluoro-1 ,4-cyclohexylene, 1 ,3-cyclohexylene, cyclopentylene, chlorocyclopentylene, fluorocyclopentylene, and cycloheptylene.

When Z' is a C6-C13 aromatic or arylalkylenic group, it can be for example m-phenylene, p-phenylene, 2-chloro-1 ,4-phenylene, 2-fluoro-1 ,4- phenylene, o-phenylene, methyl phenylene, dimethylphenylene, trimethylphenylene, tetramethyl phenylene, 1 ,4-naphthylene, 3-fluoro-1 ,4- naphthylene, 5-chloro-1 ,4-naphthylene, 1 ,5-naphtylene and 2,6- naphthylene.

[0062] Among the polyhydroxylated curing agents of formula (B),

hexafluoroisopropylidene bis (4-hydroxybenzene), known as bisphenol AF, 4,4'-dihydroxydiphenyl sulphone and isopropylidene bis (4- hydroxybenzene), known as bisphenol A, are preferred, with Bisphenol AF being particularly preferred.

[0063] Other polyhydroxylic curing agents are dihydroxy benzenes selected from the group consisting of catechol, resorcinol, 2-methyl resorcinol, 5-methyl resorcinol, hydroquinone, 2-methyl hydroquinone, 2,5-dimethyl

hydroquinone, 2-t-butyl hydroquinone, and dihydroxy naphthalenes, in particular1 ,5-dehydroxynaphthalene.

[0064] It is also understood that derivatives of aforementioned aromatic or

aliphatic polyhydroxylated compounds can be used; mention can be notably made of metal salts formed by the anion of said aromatic or aliphatic polyhydroxylated compounds wherein one or more of the hydroxyl group has been deprotonated, with one or more than one cation (as required for reaching neutrality) of a metal, typically of an alkaline or alkaline earth metal; examples thereof are notably the dipotassic salt of bisphenol AF and the monosodic monopotassic salt of bisphenol AF.

[0065] Further in addition, -onium hydroxylates, i.e. salts formed by the anion of said aromatic or aliphatic polyhydroxylated compounds wherein one or more of the hydroxyl group has been deprotonated, with one or more - onium cation can also be used. As cations, all the cations corresponding to the -onium organic derivatives accelerant components can be used.

[0066] The amount of the polydroxylated compound is generally of at least 0.5 phr, preferably at least 1 phr, and/or generally at most 15 phr, preferably at most 10 phr, with respect to the fluoroelastomer (A) weight. [0067] The composition (C) according to this second embodiment comprises at least one accelerant; accelerants for ionic curing of fluoroelastomers are well known in the art.

[0068] The accelerants suitable in the composition of the present invention are generally selected from the group consisting of organic onium compounds, amino-phosphonium derivatives, phosphoranes, imine compounds.

[0069] Organic onium compounds which are suitable in the composition of the invention generally comply with formula (O):

{[R ¹ R ² R ³ R ⁴ Q] ⁺ } _n Xi ⁿ

wherein:

- Q is selected from the group consisting of nitrogen, phosphor, arsenic, antimony, sulphur; preferably phosphor or nitrogen;

- Xi is an organic or inorganic anion, preferably selected from the group consisting of halides, sulphate, acetate, phosphate, phosphonate, hydroxide, alkoxide, phenate, bisphenate;

- n is the valence of the Xi anion;

- each of R ² , R ³ , R ⁴ , R ⁵ , equal to or different from each other, is

independently the one from the other selected from the group consisting of:

a C1-C20 alkyl group, a C6-C20 aryl group, a C6-C20 arylalkyl group, a C1-C20 alkenyl group;

a halogen selected from chlorine, fluorine, bromine;

a cyano group, a group of formula -ORB or -COORB, wherein RB is an alkyl, aryl, arylalkyl or alkenyl; wherein two groups selected from R ² ,

R ³ , R ⁴ , R ⁵ may form with Q a cyclic structure;

with the provisio that when Q is a sulphur atom one of the R ² , R ³ , R ⁴ , R ⁵ radicals is not present.

[0070] Amino-phosphonium derivatives which are suitable for use in composition (C) of this second embodiment generally comply with formula (AP-1) or (AP-2):

{[P(NR6R7) _n R8 _4.n ]÷} _q Yq- (AP-1)

{[R ⁸ 3-r(NR ⁶ R ⁷ )rP-E-P(NR ⁶ R ⁷ )rR ⁸ 3-r] ²⁺ }{Y ^q -}2/q (AP-2)

wherein: - each of R ⁶ , R ⁷ and R ⁸ , equal to or different from each other, is

independently selected from the group consisting of:

C1-C18 alkyl group (preferably C1-C12 alkyl group); C ₄ -C7 cycloalkyl group; C6-C18 aryl group (preferably C6-C12 aryl group); C6-C18 arylalkyl group (preferably C6-C ₁₂ arylalkyl group);

C ₁ -C ₁₈ oxyalkyl group comprising one or more than one hydroxyl or oxygen ethereal group;

and wherein R ⁶ , R ⁷ and R ⁸ can optionally contain halogens, CN, OH, carbalkoxy groups; wherein R ⁶ and R ⁷ can form with the nitrogen atom an heterocyclic ring;

- E is a C ₁ -C6 divalent alkylenic, oxyalkylenic or C6-C ₁₂ arylenic radical;

- n is an integer from 1 to 4;

- r is an integer from 1 to 3;

- q is the valence of the anion Y, and is preferably an integer from 1 to 2;

- Y is an organic or inorganic anion having valence q; Y can be selected from halides, perchlorate, nitrate, tetrafluoroborate, hexafluorophosphate, oxalate, acetate, stearate, haloacetate, para-toluensulphonate, phenate, bisphenate, hydroxide; Y can also be a complex anion for example ZnCI ₄ ² - , CdCU ² -, NiBr ₄ ² -, Hgl ₃ -.

[0071] Phosphoranes which are suitable in the composition (C) of this second embodiment generally comply with formula (P):

wherein:

- each of Ar’, equal to or different from each other, is a optionally substituted aryl group, preferably an optionally substituted phenyl group or an optionally substituted naphthyl group;

- each of R ¹⁰ and R ¹¹ , equal to or different from each other, is

independently selected from the group consisting of -H, -CN, Ci-Cs alkyl, - 0-C(0)-R ¹² group, -C(0)-R ¹² group, -NR ^{1 3} -C(0)-R ¹² group, with R ¹² being a C ₁ -C6 (cyclo)alkyl group, and R ^{1 3} being H or a C ₁ -C6 (cyclo)alkyl group, R ¹⁰ and R ¹¹ possibly forming together with the carbon atom of the P=C bond a cyclic group.

[0072] Imine compounds which are suitable in the composition (C) of this second embodiment generally comply with formula (I) :

[(R14) ₃ P=N = P(R14) ₃ ]÷} _Z XZ- (I)

wherein:

- R ¹⁴ , equal to or different from each other at each occurrence, is selected from the group consisting of C1-C12 hydrocarbon groups, optionally comprising one or more than one group including a heteroatom selected from the group consisting of O, N, S, halogen;

- X is an anion of valence z, with z being an integer, generally 1 or 2.

[0073] Examples of accelerants that may be used include: quaternary ammonium or phosphonium salts as notably described in EP 335705 A (MINNESOTA MINING) 4/10/1989 and US 3876654 (DUPONT) 8/04/1975 ;

aminophosphonium salts as notably described in US 4259463

(MONTEDISON SPA) 31/03/1981 ; phosphoranes as notably described in US 3752787 (DUPONT) 14/08/1973 ; imine compounds as described in EP 0120462 A (MONTEDISON SPA) 3/10/1984 or as described in EP 0182299 A (ASAHI CHEMICAL) 28/05/1986 . Quaternary phosphonium salts and aminophosphonium salts are preferred, and more preferably salts of tetrabutylphosphonium, tetrabutyl ammonium, and of 1 , 1 -diphenyl- 1 -benzyl-N-diethyl-phosphoramine of formula:

+

[0074] Instead of using the accelerator and the polyhydroxylated compound

separately, it is also possible to use an adduct between an accelerant and a polyhydroxylated compound in a mole ratio of from 1 :2 to 1 :5 and preferably from 1 :3 to 1 :5. In said adducts, the cation is hence represented by the positively charged moiety of any of the accelerants selected from the group consisting of organic onium compounds, amino-phosphonium derivatives, and imine compounds as listed above, and the anion is represented by the said polyhydroxylated curing agent, wherein one or more of the hydroxyl group has been deprotonated.

[0075] The adducts between the accelerant and the polyhydroxylated curing

agent is generally obtained by melting the product of reaction between the accelerator and the curing agent in the indicated mole ratios, or by melting the mixture of the 1 :1 adduct supplemented with the curing agent in the indicated amounts. Optionally, an excess of the accelerator, relative to that contained in the adduct, may also be present.

[0076] The following are particularly preferred as cations for the preparation of the adduct : 1 ,1-diphenyl-1-benzyl-N-diethylphosphoramine and

tetrabutylphosphonium; particularly preferred anions are those derived from bisphenol compounds in which the two aromatic rings are bonded via a divalent radical chosen from perfluoroalkyl groups of 3 to 7 carbon atoms, and the OH groups are in the para position. A method suitable for the preparation of an adduct as above described is described in European patent application EP 0684277 A (AUSIMONT SPA) 29/11/1995 , which is included herein in its entirety by reference.

[0077] The amount of the accelerant in the composition (C) according to this

second embodiment is generally of at least 0.05 phr, preferably at least 0.1 phr, and/or generally at most 10 phr, preferably at most 5 phr, with respect to the fluoroelastomer (A) weight.

[0078] The composition (C) according to this second embodiment comprises at least one basic metal oxide, which is generally selected from the group consisting of divalent metal oxides.

Among said metal oxides of divalent metals, mention can be notably made of ZnO, MgO, PbO, and their mixtures, with MgO being preferred.

[0079] The amount of the basic metal oxide is generally of at least 0.5 phr,

preferably at least 1 phr, and/or generally at most 25 phr, preferably at most 15 phr, more preferably at most 10 phr, with respect to the

fluoroelastomer (A) weight. [0080] The composition (C) according to this second embodiment optionally comprises at least one metal hydroxide, with the provision that if said metal hydroxide is present, its amount is preferably below 6 phr, more preferably below 3 phr based on 100 weight parts of fluoroelastomer (A).

[0081] Hydroxides which can be used are generally selected from the group

consisting of Ca(OH)2, Sr(OH)2, Ba(OH)2.

[0082] It is generally understood that performances of the composition (C) of this second embodiment can be optimized wherein the amount of metal hydroxide(s) is advantageously below 2.5 phr, preferably below 2 phr, more preferably below 1 phr, including when no metal hydroxide(s) is used, based on 100 weight parts of fluoroelastomer (A).

[0083] Whichever is the crosslinking system comprised in the composition (C), other conventional additives, such as fillers, thickeners, pigments, antioxidants, stabilizers, processing aids/plasticizers, and the like may be present. Carbon black is often used as an advantageous reinforcing system.

[0084] As said, the composition (C) may include at least one plasticizer (P),

generally selected from those known for fluororubbers. Plasticizers (P) will be generally selected among ester-based plasticizers, such as glutarates (e.g. Diisodecyl glutarate), adipates (e.g. Bis(2-ethylhexyl)adipate, dimethyl adipate, monomethyl adipate, dioctyl adipate,

Dibutoxyethoxyethyl adipate, Dibutoxyethyl adipate, Diisodecyl adipate), maleates (e.g. dibutyl maleate; diisobutyl maleate), azelates, sebacates (e.g. dibutyl sebacate, Di-2-ethylhexyl sebacate), trimellitates (e.g. tri-2- ethylhexyl trimellitate), citrates (e.g. triethyl citrate, tributyl citrate, acetyltriethylcitrate, acetyl tributyl citrate, trioctyl citrate, acetyl trioctyl citrate, trihexyl citrate, acetyl trihexyl citrate), phosphate esters (e.g.

triethyl phosphate, tributyl phosphate, trioctyl phosphate).

[0085] The invention further pertains to a process for the manufacture of

composition (C), as above detailed, said method comprising mixing:

- the fluoroelastomer (A);

- the cross-linking system; and

- the polymer (PAI). [0086] Still, the invention pertains to a method for fabricating shaped articles comprising curing the composition (C), as above described.

[0087] The composition (C) can be fabricated, e.g. by moulding (injection

moulding, extrusion moulding), calendering, coating, screen-printing, forming-in-place, into the desired shaped article, which is advantageously subjected to vulcanization (curing) during the processing itself and/or in a subsequent step (post-treatment or post-cure), advantageously

transforming the relatively soft, weak, fluoroelastomeric uncured

composition into a finished article made of non-tacky, strong, insoluble, chemically and thermally resistant cured fluoroelastomer material.

[0088] Yet, the invention pertains to cured articles obtained from the composition (C), as above detailed. Said cured articles are generally obtained by moulding and curing the fluoroelastomer composition, as above detailed. These cured articles may be sealing articles, including 0(square)-rings, packings, gaskets, diaphragms, shaft seals, valve stem seals, piston rings, crankshaft seals, cam shaft seals, and oil seals or maybe piping and tubings, in particular flexible hoses or other items, including conduits for delivery of hydrocarbon fluids and fuels.

[0089] Finally, the invention further pertains to assemblies including a substrate and at least one cured article, as above detailed.

[0090] The choice of substrate is not particularly limited: the composition (C) of the invention is such to ensure adhesion to a variety of metal and non- metal substrates, including notably plastic and rubber substrates, among which polyamide substrates, silicone substrates can be notably mentioned.

[0091] The assemblies of the invention are generally manufactured by contacting the composition (C), as above detailed, with a substrate, and subjecting the said composition (C) to vulcanization (curing) while in contact with the said substrate, and optionally exposing the assembly to a subsequent thermal treatment step (post-treatment or post-cure).

[0092] Should the disclosure of any of the patents, patent applications, and

publications that are incorporated herein by reference conflict with the present description to the extent that it might render a term unclear, the present description shall take precedence. [0093] The present invention will be now described in more detail with reference to the following examples, whose purpose is merely illustrative and not limitative of the scope of the invention.

[0094] EXAMPLES

[0095] Raw materials

[0096] Tecnoflon® P X647 is an iodine-containing peroxide curable

fluoroelastomer commercially available from Solvay Specialty Polymers Italy, SpA.

[0097] VAROX® DBPH-50 is 2,5-dimethyl-2,5-di (t-butylperoxy)-hexane,

available from R. T. Vanderbilt, Norwalk, Conn.

[0098] TAIC DLC-A is a triallyl isocyanurate, silicon-dioxide blend co-agent for peroxide vulcanization, comprising about 72 % wt TAIC, commercially available from NATROCHEM, INC.

[0099] N550 BLACK is a N550 semi-reinforcing carbon black commercially

available notably from MAKROChem.

[0100] ARMEEN 18D is distilled octadecylamine commercially available from Akzo Nobel.

[0101] Torlon® AI-10 is a powdered aromatic polyamideimide commercially available from Solvay Specialty Polymers USA, LLC.

[0102] Torlon® 4000TF is a neat resin aromatic polyamide-imide (PAI) fine

powder designed for compounding with other polymers and specialty additives, commercially available from Solvay Specialty Polymers USA, LLC.

[0103] Adhesion to Silicone

[0104] Comparative Example 1 A

[0105] A commercial Tecnoflon® grade P X647, compounded as in Table 1 , was placed into an ASTM slab mold over a silicone compound. For an half of the slab wax paper was placed so as to keep the silicone and FKM compound joining together in the remaining uncovered part. Then, we closed the mold and added a 25 lb weight on top of the mold to close it. The system was pressed cured for 30 minutes at 177 deg C.

[0106]

Table 1

[0107] Example 1

[0108] A commercial Tecnoflon® grade P X647 was blended in open mill with 6 phr of commercial Torlon® AI-10 obtaining the Polymer A. Polymer A was compounded in open mill according to the recipe in Table 2. The material was then molded with silicone as described in Comparative Ex 1.

[0109]

Table 2

[01 10] Example 2

[01 1 1] A commercial Tecnoflon® grade P X647 was blended in open mill with 6 phr of commercial Torlon® 4000TF obtaining the Polymer B. Polymer B was compounded in open mill according to the recipe in Table 3. The material was then molded with silicone as described in Comparative Ex 1.

[01 12]

Table 3

[01 13] Adhesion to Stainless Steel

[01 14] Adhesion property of Tecnoflon® PX 647, Polymer A and Polymer B against Stainless Steel was measured according to the following molding procedure.

[01 15] A sand blasted stainless steel plaque was placed in ASTM D429-Method B slab mold with FKM compound. For an half of the slab a wax paper so as to keep the stainless steel and FKM compound joining together in the remaining uncovered part. Then, the assembled mold was closed into a standard compression molding machine. It was cured for 30 minutes at 177 deg C.

[01 16]

Table 4

After press cure: 10' @ 177°C

Adhesion to Silicon according the

ASTM D1876 180° Peel Test

Adhesion after Heat Resistance, 168 hours @ 200°C:

Adhesion after Heat Resistance, 168 hours @ 230°C:

Adhesion to Stainless steel according to ASTM D429 Method B

Initial Adhesion after press cure: