This application claims priority to European application No. 09172280.1 filed Oct. 6, 2009, the whole content of this application being incorporated herein by reference for all purposes.
The present invention relates to (per)fluoropolyether lubricant compositions and use thereof for lubricating vacuum pumps.
Fluoropolyether lubricants are known in the art for being used in vacuum pumps in highly demanding applications, e.g. in the semiconductor industry, in particular for lubricating compressors and pumps handling reactive and hazardous gases, typically in rotary pumps, turbomolecular pumps, roots pumps and diffusion pumps.
Actually, major requirements for fluoropolyether lubricants to be employed for high vacuum and ultra-high vacuum applications include high thermal-oxidative stability in the presence of metals, low evaporation weight loss and high lubrication performances.
Fluoropolyether oils substantially free from volatile fractions are typically used for lubricating vacuum pumps so that back migration of the volatile oil fractions into the vacuum chamber, which is commonly due to heat generated by friction among the moving metallic parts while operating, is generally reduced.
Thus, EP 0553768 B (AUSIMONT S.P.A.) May 3, 2000 discloses use in vacuum pumps of perfluoropolyethers having at most 0.1% by weight of fractions exhibiting a molecular weight lower than or equal to 1500 and at most 1.3% by weight of fractions exhibiting a molecular weight lower than or equal to 1800, said perfluoropolyethers being typically endowed with a viscosity ranging from about 140 cSt to about 270 cSt at 20° C. and preferably complying with branched perfluoropolyethers having formulae CF3(OCF(CF3)CF2)m(OCF2)mOCF3, wherein m/n is equal to or higher than 1000, and F(CF2CF(CF3)O)qCF2CF3.
Nevertheless, fluoropolyether oils of the prior art, in particular linear fluoropolyether oils generally suffer from low thermal-oxidative stability in the presence of metals to be advantageously used as lubricants in high vacuum and ultra-high vacuum pumps.
EP 1454938 B (SOLVAY SOLEXIS S.P.A.) May 10, 2005 discloses linear perfluoropolyether oils comprising —CF2CF2O— and —CF2O— recurring units, statistically distributed along the perfluoropolyoxyalkylene chain, in a —CF2 CF2O—/—CF2O— ratio comprised between 2 and 20, which exhibit improved thermal-oxidative stability in the presence of metals with respect to known linear perfluoropolyether oils having a lower —CF2CF2O—/—CF2O— ratio, typically comprised between 0.1 and 10, while maintaining a high viscosity index and a low pour point value as compared with known linear perfluoropolyether oils. The stability of the novel linear perfluoropolyether oils when used as lubricants may be further increased by the addition of perfluoropolyether-based thermal stabilizers comprising functional groups like, e.g., phosphines, phosphates, phosphazenes, benzothiazoles, triazines, amines, substituted amines, nitroderivative compounds.
The need was thus felt to provide for (per)fluoropolyether lubricants having improved thermal-oxidative stability in the presence of metals while maintaining low evaporation weight loss and high lubrication performances in terms of suitable kinematic viscosity and anti-wear and anti-rust properties, so as to be successfully used in high vacuum and ultra-high vacuum pumps by ensuring lower maintenance costs of the pumps due to a longer life-time of the lubricants and lower consumptions due to their high lubrication performances.
It is thus an object of the invention a lubricant composition comprising:
(A) at least one non-functional (per)fluoropolyether oil (non-functional PFPE oil) comprising at least one (per)fluoropolyoxyalkylene chain (chain RF);
(B) at least one cyclic phosphazene compound [compound (P)] comprising one or more cyclic moieties having formula (I) or (II) here below:
said cyclic moieties comprising, bound to one or more phosphorus atoms, at least one substituent comprising at least one (per)fluoropolyoxyalkylene chain (chain R′F);
(C) at least one functional (per)fluoropolyether derivative (functional PFPE derivative) different from compound (P) comprising at least one (per)fluoropolyoxyalkylene chain (chain R′F) and at least one functional group comprising at least one monocyclic or polycyclic aromatic ring, said aromatic ring optionally containing one or more heteroatoms selected from N, O and S and one or more substituents different from hydrogen atoms.
The Applicant has surprisingly found that the lubricant composition of the invention advantageously exhibits improved thermal-oxidative stability in the presence of metals while maintaining low evaporation weight loss and high lubrication performances to be successfully used for high vacuum and ultra-high vacuum applications.
To the purpose of the present invention, “(per)fluoropolyether” is intended to denote either a fully fluorinated perfluoropolyether or a partially fluorinated fluoropolyether.
To the purpose of the present invention, “(per)fluoropolyoxyalkylene chain” is intended to denote either a fully fluorinated perfluoropolyoxyalkylene chain or a partially fluorinated fluoropolyoxyalkylene chain.
The (per)fluoropolyoxyalkylene chain (chain RF) of the non-functional (per)fluoropolyether oil (non-functional PFPE oil) of the invention typically comprises one or more recurring units Ro having general formula —(CJJ′)j—CKK′—O—, wherein J and J′, equal to or different from each other, independently represent a fluorine atom or a C1-C6 (per)fluoro(oxy)alkyl group, K and K′, equal to or different from each other, independently represent a hydrogen atom, a fluorine atom, a chlorine atom or a C1-C6 (per)fluoro(oxy)alkyl group and j is an integer comprised between 0 and 3, said recurring units being generally statistically distributed along the (per)fluoropolyoxyalkylene chain.
The non-functional PFPE oil of the invention may be a linear non-functional PFPE oil or a branched non-functional PFPE oil.
By “linear non-functional PFPE oil” it is meant a non-functional PFPE oil comprising at least one (per)fluoropolyoxyalkylene chain (chain RF) as defined above, wherein J and J′ both represent a fluorine atom and K and K′, equal to or different from each other, independently represent a hydrogen atom, a fluorine atom or a chlorine atom.
By “branched non-functional PFPE oil” it is meant a non-functional PFPE oil comprising at least one (per)fluoropolyoxyalkylene chain (chain RF) as defined above, wherein at least one of J, J′, K and K′ represents a C1-C6 (per)fluoro(oxy)alkyl group.
Representative examples of suitable non-functional PFPE oils according to the invention include, notably, the followings:
T1-O—(C2F4O)b1′(CF2O)b2′-T1′ (1)
wherein:
T2-O—(CF2O)c1′(CF2CF2O)c2′(CF2CF2CF2O)c3′(CF2CF2CF2CF2O)c4′-T2′ (2)
wherein:
Said products can be produced as described in EP 1454938 B (SOLVAY SOLEXIS S.P.A.) Oct. 5, 2005.
T3-O—(CF2CF2O)d′-T3′ (3)
wherein:
Said products can be obtained by a method comprising fluorinating a polyethyleneoxide, e.g. with elemental fluorine, and optionally thermally fragmentating the so-obtained fluorinated polyethyleneoxide as reported in U.S. Pat. No. 4,523,039 (THE UNIVERSITY OF TEXAS) Jun. 11, 1985.
T1-O—(CF2CF2C(Hal)2O)e1′—(CF2CF2CH2O)e2′—(CF2CF2CH(Hal)O)e3′-T (4)
wherein:
Said products may be prepared by ring-opening polymerizing 2,2,3,3-tetrafluorooxethane in the presence of a polymerization initiator to give a polyether comprising repeating units of the formula: —CH2CF2CF2O—, and optionally fluorinating and/or chlorinating said polyether, as detailed in EP 148482 B (DAIKIN INDUSTRIES LTD.) Mar. 25, 1992.
T1-O—[CF(CF3)CF2O]f1′(CFYO)f2′-T1′ (5)
wherein:
Said products can be obtained by photooxidation of C3F6 as described in CA 786877 (MONTEDISON S.P.A.) Jun. 4, 1968 and by subsequent conversion of the end groups as described in GB 1226566 (MONTECATINI EDISON S.P.A.) Mar. 31, 1971.
T1-O—[CF(CF3)CF2O]g1′(C2F4O)g2′(CFYO)g3′-T1′ (6)
wherein:
Said products can be manufactured by photooxidation of a mixture of C3F6 and C2F4 and subsequent treatment with fluorine as described in U.S. Pat. No. 3,665,041 (MONTECATINI EDISON S.P.A.) May 23, 1972.
C3F7O—[CF(CF3)CF2O]h′-T3 (7)
wherein:
Said products can be prepared by ionic hexafluoropropylene epoxide oligomerization and subsequent treatment with fluorine as described in U.S. Pat. No. 3,242,218 (E. I. DU PONT DE NEMOURS AND CO.) Mar. 22, 1966.
{C3F7O—[CF(CF3)CF2O]i′—CF(CF3)—}2 (8)
wherein:
Said products can be obtained by ionic telomerization of the hexafluoropropylene epoxide and subsequent photochemical dimerization as reported in U.S. Pat. No. 3,214,478 (E. I. DU PONT DE NEMOURS AND CO.) Oct. 26, 1965.
R1f—{C(CF3)2—O—[C(R2f)2]j1′C(R2f)2—O}j2′—R1f (9)
wherein:
Said products can be produced by the copolymerization of hexafluoroacetone with an oxygen-containing cyclic comonomer selected from ethylene oxide, propylene oxide, epoxy-butane and/or trimethylene oxide (oxethane) or substituted derivatives thereof and subsequent perfluorination of the resulting copolymer, as detailed in patent application WO 87/00538 (LAGOW ET AL.) Jan. 1, 1987.
Preferred non-functional PFPE oils suitable for the purpose of the invention include, notably, the followings:
(i) non-functional PFPE oils complying with formula (2) as described above, wherein:
CF3—[(OCF2CF2)m—(OCF2)n]—OCF3
m+n=40-180; m/n=0.5-2
CF3[(OCF(CF3)CF2)p—(OCF2)q]—OCF3
p+q=8-45; p/q=20-1000
(iii) non-functional PFPE oils commercially available from Daikin under the trade name DEMNUM®, said oils generally comprising at least one oil complying with formula here below:
F—(CF2CF2CF2O)n—(CF2CF2CH2O)j—CF2CF3
j=0 or integer >0; n+j=10-150
(iv) non-functional PFPE oils commercially available from Du Pont de Nemours under the trade name KRYTOX®, said oils generally comprising at least one low-molecular weight, fluorine end-capped, homopolymer of hexafluoropropylene epoxide complying with formula here below:
F—(CF(CF3)CF2O)n—CF2CF3
n=10-60
More preferred non-functional PFPE oils suitable for the purpose of the invention include, notably, non-functional PFPE oils complying with formula (2) as described hereinabove and non-functional PFPE oils commercially available from Solvay Solexis S.p.A. under the trade name FOMBLIN® (type M, Z or Y) as described hereinabove.
A mixture of more than one non-functional PFPE oil as defined above may also be used in the lubricant composition of the invention.
Preferred mixtures of more than one non-functional PFPE oil as defined above include, notably, mixtures of at least one linear non-functional PFPE oil as defined above with at least one branched non-functional PFPE oil as defined above. Representative examples of suitable mixtures of at least one linear non-functional PFPE oil as defined above with at least one branched non-functional PFPE oil as defined above include, notably, those commercially available from Solvay Solexis S.p.A. under the trade name FOMBLIN® W.
The (per)fluoropolyoxyalkylene chain (chain R′F) of the cyclic phosphazene compound [compound (P)] of the invention typically comprises one or more recurring units R1 having general formula —(CF2)j—CFK—O—, wherein K is selected from a fluorine atom and a C1-C5 (per)fluoro(oxy)alkyl group and j is an integer comprised between 0 and 3, said recurring units being generally statistically distributed along the (per)fluoropolyoxyalkylene chain.
According to a first embodiment of the invention, the compound (P) complies with formula (I-A), (I-A bis) or (II-A) here below:
wherein:
Compounds (P) complying with formula (I-A), (I-A bis) or (II-A) as described in this first embodiment of the invention are notably disclosed in EP 1336614 A (SOLVAY SOLEXIS S.P.A.) Aug. 20, 2003.
According to a second embodiment of the invention, the compound (P) complies with formula (I-B) or (II-B) here below:
wherein:
said recurring units being generally statistically distributed along the (per)fluoropolyoxyalkylene chain;
The compound (P) of this second embodiment of the invention preferably complies with formula (I-B) or (II-B) here above, wherein R″fO— and R′″fO— are selected from:
T4-O—(CF2CF2O)p′(CF2O)q′-J- (a)
wherein:
T5-O—(CF2CF(CF3)O)r′—(CF2CF2O)s′—(CFYO)t′-J- (b)
wherein:
T5-(OCFY)t1″(OC3F6)u1″—OR*fO—(C3F6O)u2″(CFYO)t2″-J- (c)
wherein:
T4-CF2CF2O—(CF2—(CF2)x′CF2O)v′-J- (d)
wherein:
T4-CF2CH2—(OCF2CF2CH2)w′—OR*fO—(CH2CF2CF2O)w′-J- (e)
wherein:
The compound (P) of this second embodiment of the invention more preferably complies with formula (I-B*) or (II-B*) here below:
wherein:
T*-O—(CF2CF2O)p*(CF2O)q*-CF2—CH2—O—(CH2CH2O)s*—
wherein:
The compound (P) of this second embodiment of the invention most preferably complies with formula (III-B) or (III-B bis) here below:
wherein:
Compounds (P) complying with formula (I-B) or (II-B) as described in this second embodiment of the invention are notably disclosed in WO 2008/000706 (SOLVAY SOLEXIS S.P.A.) Jan. 3, 2008.
According to a third embodiment of the invention, the compound (P) typically complies with formula (IV-C) here below:
wherein:
Compounds (P) complying with formula (IV-C) as described in this third embodiment of the invention are notably disclosed in EP 0597369 A (AUSIMONT S.P.A.) Sep. 16, 1998.
Preferred lubricant compositions of the invention comprise one or more compounds (P) according to the first and/or the second embodiment of the invention as detailed above.
More preferred lubricant compositions of the invention comprise one or more compounds (P) according to the second embodiment of the invention as detailed above.
Most preferred lubricant compositions of the invention comprise one or more compounds (P) complying with either of formulae (III-B) or (III-B bis) as described above.
The functional (per)fluoropolyether derivative (functional PFPE derivative) of the invention comprises at least one (per)fluoropolyoxyalkylene chain (chain R′F) as defined above and at least one functional group typically comprising at least one ether, thioether, ester or amine group comprising at least one monocyclic or polycyclic aromatic ring, said aromatic ring optionally containing one or more heteroatoms selected from N, O and S and one or more substituents different from hydrogen atoms.
The functional (per)fluoropolyether derivative (functional PFPE derivative) of the invention preferably complies with formula (V) here below:
T-(CFW1)p1—O—RF—(CFW2)p1′-T′ (V)
wherein:
The functional PFPE derivative of the invention more preferably complies with formula (VI) here below:
T″-CF2O(CF2CF2O)m—(CF2O)n—CF2-T′″ (VI)
wherein:
Preferred lubricant compositions of the invention comprise one or more functional PFPE derivatives selected from:
Most preferred lubricant compositions of the invention comprise one or more functional PFPE derivatives complying with formula (VI) as described above wherein both T″ and T′″ are functional end-groups as defined above (bifunctional PFPE derivatives).
Non-limitative examples of suitable bifunctional PFPE derivatives include, notably, the followings:
wherein m* and n* are integers such that the number average molecular weight of the bifunctional PFPE derivative is comprised between 1000 and 6000, preferably between 2000 and 4000, the m/n ratio being comprised between 0.1 and 5;
wherein m* and n* are integers such that the number average molecular weight of the bifunctional PFPE derivative is comprised between 1000 and 6000, preferably between 2000 and 4000, the m/n ratio being comprised between 0.1 and 5.
Very good results have been obtained with lubricant compositions comprising one or more bifunctional PFPE derivatives complying with formula here below:
wherein m* and n* are integers such that the number average molecular weight of the bifunctional PFPE derivative is comprised between 1000 and 6000, preferably between 2000 and 4000, the m/n ratio being comprised between 0.1 and 5.
The lubricant composition of the invention typically comprises at least one cyclic phosphazene compound [compound (P)] as defined above in an amount of at least 0.1% by weight, preferably at least 0.2% by weight, more preferably at least 0.3% by weight with respect to the weight of the non-functional PFPE oil.
The lubricant composition of the invention typically comprises at least one cyclic phosphazene compound [compound (P)] as defined above in an amount of at most 15% by weight, preferably at most 10% by weight, more preferably at most 5% by weight with respect to the weight of the non-functional PFPE oil.
The lubricant composition of the invention typically comprises at least one functional PFPE derivative different from compound (P) as defined above in an amount of at least 0.5% by weight, preferably at least 1% by weight, more preferably at least 2% by weight with respect to the weight of the non-functional PFPE oil.
The lubricant composition of the invention typically comprises at least one functional PFPE derivative different from compound (P) as defined above in an amount of at most 15% by weight, preferably at most 10% by weight, more preferably at most 6% by weight with respect to the weight of the non-functional PFPE oil.
Very good results have been obtained with lubricant compositions comprising at least one cyclic phosphazene compound [compound (P)] in an amount ranging from 0.3% to 5% by weight with respect to the weight of the non-functional PFPE oil and at least one functional PFPE derivative different from compound (P) as defined above in an amount ranging from 2% to 6% by weight with respect to the weight of the non-functional PFPE oil.
The lubricant composition of the invention typically has a kinematic viscosity (η) ranging from 100 to 350, preferably from 120 to 300, as measured at 20° C. by ASTM D445.
The lubricant composition can also further comprise other additives notably including one or more anti-rust additives, oxidation inhibitors, antifoam agents, anti-wear additives and anti-scuff additives. Representative examples of anti-rust additives which can be advantageously added to the lubricant composition of the invention include, notably, functional PFPEs commercially available from Solvay Solexis S.p.A. under the trade names FOMBLIN® DA305, FOMBLIN® DA306 and FOMBLIN® DA308.
Another object of the invention is use of the lubricant composition as described above for lubricating vacuum pumps, in particular high vacuum and ultra-high vacuum pumps, especially in the semiconductor industry where high-purity lubricants are typically required.
Should the disclosure of any patents, patent applications, and publications which are incorporated herein by reference conflict with the description of the present application to the extent that it may render a term unclear, the present description shall take precedence.
The 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.
The non-functional PFPE oil (1) is a linear non-functional PFPE oil having formula CF3O—(CF2O)n(CF2CF2O)m(CF2CF2CF2O)r(CF2CF2CF2CF2O)s—CF3, wherein m, n, r and s are integers such that the number average molecular weight is about 11000, the m/n ratio being about 2.7.
The non-functional PFPE oil (2) is a FOMBLIN® M15 linear non-functional PFPE oil having formula CF3O—(CF2CF2O)m(CF2O)n—CF3, wherein m and n are integers such that the number average molecular weight is about 10600, the m/n ratio being about 0.9.
The non-functional PFPE oil (3) is a FOMBLIN® M30 linear non-functional
PFPE oil having formula CF3O—(CF2CF2O)m(CF2O)n—CF3, wherein m and n are integers such that the number average molecular weight is about 13000, the m/n ratio being about 0.9.
The non-functional PFPE oil (4) is a FOMBLIN® Y25/6 branched non-functional PFPE oil having formula
CF3O—(CF(CF3)CF2O)p(CF2O)q—CF3, wherein p and q are integers such that the number average molecular weight is about 3800.
The compound (P1) is a cyclic phosphazene compound having formula
wherein p*i (i=1 to 5) and q*i (i=1 to 5) indexes are integers such that the number average molecular weight is about 8300.
The functional PFPE derivative (1) has formula
wherein m and n are integers such that the number average molecular weight is about 3800, the m/n ratio being about 0.9.
Thermal-oxidative stability tests were conducted on a sintered metal bearing of Fe—Cu—Sn—C type.
The sintered metal bearing of Fe—Cu—Sn—C type was impregnated with the lubricant composition of the invention at 30° C., under vacuum (7 mbar), for 25 minutes. The sintered metal bearing so treated was then allowed to drain for about 15 minutes, so that the amount of lubricant composition impregnated in the sintered metal bearing was about 0.05 g.
The sintered metal bearing so impregnated was placed in a ventilated oven set at 200° C. and weighted every 48-72 hours.
Weight loss of the lubricant composition was checked as a function of time.
An induction time was measured until complete degradation of the lubricant composition.
Sliding wear tests were conducted with a ball-on-disk tribometer at 140° C. during 6 hours under the following operating conditions:
The wear volume (V) on the disk [mm3] has been calculated as follows:
wherein:
A lubricant composition was prepared by mixing non-functional PFPE oil (3) with 0.5% by weight of non-functional PFPE oil (3) of compound (P1) and 5% by weight of non-functional PFPE oil (3) of functional PFPE derivative (1).
The results for the thermal-oxidative stability test of said lubricant composition are set forth in Table 1 here below.
A composition was prepared by mixing non-functional PFPE oil (3) with 0.5% by weight of non-functional PFPE oil (3) of compound (P1).
The results for the thermal-oxidative stability test of said composition are set forth in Table 1 here below.
A composition was prepared by mixing non-functional PFPE oil (3) with 5% by weight of non-functional PFPE oil (3) of functional PFPE derivative (1).
The results for the thermal-oxidative stability test of said composition are set forth in Table 1 here below.
The thermal-oxidative stability tests performed with the lubricant composition of Example 1 of the invention showed a substantial increase of the induction time to degradation with respect to compositions of comparative Examples 1C and 2C, that is to say that the lubricant composition of the invention showed improved thermal-oxidative stability with respect to compositions comprising at least one non-functional PFPE oil as defined above and either at least one compound (P) as defined above or at least one functional PFPE derivative as defined above.
A lubricant composition was prepared by mixing non-functional PFPE oil (1) with 3% by weight of non-functional PFPE oil (1) of compound (P1) and 3% by weight of non-functional PFPE oil (1) of functional PFPE derivative (1).
The results for the tribological test and the evaporating constant at 150° C. [(mm3 of evaporated lubricant/mm2 of exposed surface area)·h] ([*]) of said lubricant composition are set forth in Table 2 here below.
A lubricant composition was prepared by mixing non-functional PFPE oil (2) with 3% by weight of non-functional PFPE oil (2) of compound (P1) and 3% by weight of non-functional PFPE oil (2) of functional PFPE derivative (1).
The results for the tribological test and the evaporating constant at 150° C. [(mm3 of evaporated lubricant/mm2 of exposed surface area)·h] ([*]) of said lubricant composition are set forth in Table 2 here below.
A lubricant composition was prepared by mixing non-functional PFPE oil (4) with 3% by weight of non-functional PFPE oil (4) of compound (P1) and 3% by weight of non-functional PFPE oil (4) of functional PFPE derivative (1).
The results for the tribological test and the evaporating constant at 150° C. [(mm3 of evaporated lubricant/mm2 of exposed surface area)·h] ([*]) of said lubricant composition are set forth in Table 2 here below.
A composition was prepared by mixing non-functional PFPE oil (2) with 3% by weight of non-functional PFPE oil (2) of compound (P1).
The results for the tribological test and the evaporating constant at 150° C. [(mm3 of evaporated lubricant/mm2 of exposed surface area)·h] ([*]) of said composition are set forth in Table 2 here below.
The thermal-oxidative stability tests performed with the composition of Example 3C showed a substantial decrease of the induction time to degradation with respect to the lubricant composition of Example 4 of the invention.
A composition was prepared by mixing non-functional PFPE oil (2) with 3% by weight of non-functional PFPE oil (2) of functional PFPE derivative (1).
The results for the tribological test and the evaporating constant at 150° C. [(mm3 of evaporated lubricant/mm2 of exposed surface area)·h] ([*]) of said composition are set forth in Table 2 here below.
The thermal-oxidative stability tests performed with the composition of Example 4C showed a substantial decrease of the induction time to degradation with respect to the lubricant composition of Example 4 of the invention.
Substantially low wear volumes and low evaporating constants were measured for the lubricant compositions of Examples 2, 3 and 4 of the invention, that is to say that the lubricant compositions of the invention exhibited substantially high lubrication performances in terms of anti-wear properties and low evaporation weight loss. In particular, the tribological tests performed with the lubricant composition of Example 3 of the invention showed that substantially low or even slightly decreased wear volumes were measured with respect to compositions of comparative Examples 3C and 4C, that is to say that the lubricant composition of the invention showed good or slightly improved anti-wear properties with respect to compositions comprising at least one non-functional PFPE oil as defined above and either at least one compound (P) as defined above or at least one functional PFPE derivative as defined above.
Number | Date | Country | Kind |
---|---|---|---|
09172280.1 | Oct 2009 | EP | regional |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP2010/064686 | 10/1/2010 | WO | 00 | 4/3/2012 |