US20090286705A1 - Flame retardant lubricating oil compositions - Google Patents
Flame retardant lubricating oil compositions Download PDFInfo
- Publication number
- US20090286705A1 US20090286705A1 US12/383,407 US38340709A US2009286705A1 US 20090286705 A1 US20090286705 A1 US 20090286705A1 US 38340709 A US38340709 A US 38340709A US 2009286705 A1 US2009286705 A1 US 2009286705A1
- Authority
- US
- United States
- Prior art keywords
- base oil
- fluids
- pour point
- fluid
- gtl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims description 17
- 239000003063 flame retardant Substances 0.000 title claims description 17
- 239000000203 mixture Substances 0.000 title abstract description 26
- 239000010687 lubricating oil Substances 0.000 title abstract description 6
- 239000012530 fluid Substances 0.000 claims abstract description 97
- 239000002199 base oil Substances 0.000 claims abstract description 40
- 230000000994 depressogenic effect Effects 0.000 claims abstract description 12
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 5
- -1 dicarboxylic acid ester Chemical class 0.000 abstract description 13
- 239000000654 additive Substances 0.000 abstract description 5
- 230000000996 additive effect Effects 0.000 abstract 1
- 229920013639 polyalphaolefin Polymers 0.000 description 22
- 150000002430 hydrocarbons Chemical class 0.000 description 20
- 241001594857 Pao Species 0.000 description 19
- 229930195733 hydrocarbon Natural products 0.000 description 17
- 239000004215 Carbon black (E152) Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- 239000001993 wax Substances 0.000 description 11
- 150000002148 esters Chemical class 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 239000000539 dimer Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 229910019142 PO4 Inorganic materials 0.000 description 6
- 230000009970 fire resistant effect Effects 0.000 description 6
- 239000002480 mineral oil Substances 0.000 description 6
- 235000021317 phosphate Nutrition 0.000 description 6
- 229920005862 polyol Polymers 0.000 description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 235000010446 mineral oil Nutrition 0.000 description 5
- 150000003077 polyols Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229910001868 water Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 241000282326 Felis catus Species 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000001747 exhibiting effect Effects 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- 239000013638 trimer Substances 0.000 description 4
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 229920000193 polymethacrylate Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- 101150092791 PAO4 gene Proteins 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 2
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 239000010720 hydraulic oil Substances 0.000 description 2
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
- 235000021313 oleic acid Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ALKCLFLTXBBMMP-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl hexanoate Chemical compound CCCCCC(=O)OC(C)(C=C)CCC=C(C)C ALKCLFLTXBBMMP-UHFFFAOYSA-N 0.000 description 1
- SIXWIUJQBBANGK-UHFFFAOYSA-N 4-(4-fluorophenyl)-1h-pyrazol-5-amine Chemical compound N1N=CC(C=2C=CC(F)=CC=2)=C1N SIXWIUJQBBANGK-UHFFFAOYSA-N 0.000 description 1
- HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 description 1
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 1
- QDTDKYHPHANITQ-UHFFFAOYSA-N 7-methyloctan-1-ol Chemical compound CC(C)CCCCCCO QDTDKYHPHANITQ-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical class OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- 239000004439 Isononyl alcohol Substances 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 239000007866 anti-wear additive Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- CJFLBOQMPJCWLR-UHFFFAOYSA-N bis(6-methylheptyl) hexanedioate Chemical compound CC(C)CCCCCOC(=O)CCCCC(=O)OCCCCCC(C)C CJFLBOQMPJCWLR-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000013538 functional additive Substances 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- TYFQFVWCELRYAO-UHFFFAOYSA-L suberate(2-) Chemical compound [O-]C(=O)CCCCCCC([O-])=O TYFQFVWCELRYAO-UHFFFAOYSA-L 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- 229940057402 undecyl alcohol Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
- C10M169/041—Mixtures of base-materials and additives the additives being macromolecular compounds only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M111/00—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
- C10M111/04—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
- C10M2205/0285—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/17—Fisher Tropsch reaction products
- C10M2205/173—Fisher Tropsch reaction products used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
- C10M2207/2825—Esters of (cyclo)aliphatic oolycarboxylic acids used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/06—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
- C10M2209/062—Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/02—Pour-point; Viscosity index
Definitions
- the present invention relates to hydraulic fluids exhibiting flame retardant properties and good low temperature viscometrics.
- HFA which are high water content fluids, >80% water
- HFB which are water-in-oil emulsions, ⁇ 50% water
- HFC which are water-glycol fluids, 30-80% water
- HFD-R which are phosphate ester fluids
- HFD-U which are all other, including polyol ester-based fluids, vegetable oil ester-based fluids, fluorocarbon-based fluids, silicate ester-based fluids, silicone-based fluids and PAO-based fluids.
- U.S. Pat. No. 3,793,207 teaches fire-resistant hydraulic fluids having improved low temperature characteristics; e.g., viscosity, pour point, and cloud point which consist mainly of a mixture of a hydrocarbon base oil, preferably a synthetic hydrocarbon, a dialkyl carboxylate ester and an ortho-silicate.
- the synthetic hydrocarbon oil constitutes the base oil of the composition
- the ester of a dicarboxylic acid constitutes 20-30 wt % of the composition
- the alkyl silicate constitutes 10-15 wt % of the composition, with small percentages of other functional additives being present, such as anti-wear agents, hydrolysis suppressants, anti-foamants, etc.
- the hydrocarbon oil employed has a viscosity of from 8,500 to 10,800 cs at ⁇ 40° F., 25-35 cs at 100° F., and 4-8 cs at 210° F., and is preferably a dialkylaromatic hydrocarbon.
- the preferred ester of a dicarboxylic acid is a dialkyl adipate ester of a C 6 -C 10 alcohol.
- the fluid is hydrolytically stable, has excellent low temperature viscometrics and has a high flash point, fire point and autogenous ignition temperature.
- U.S. Pat. No. 3,873,464 teaches a flame resistant hydraulic fluid comprising a major amount of a synthetic hydrocarbon oil having at least 30 carbon atoms in each molecule, and a small amount of a mixture comprising chlorinated polyphenyls and a trihydrocarbon phosphate.
- the synthetic hydrocarbon base oil is of the type made by polymerizing olefins in the presence of a suitable catalyst, such as BF 3 or AlCl 3 .
- the preferred synthetic hydrocarbon oil is a trimer of decene.
- U.S. Pat. No. 6,361,711 teaches a flame retardant hydraulic oil containing a hydraulic base oil including as essential component a synthetic ester formed by reacting at least one polyol selected from the group consisting of neopentyl glycol, 2,2-dimethyl-3-hydroxy propyl-2′,2′-dimethyl-3′-hydroxypropionate, glycerine and trimethylolpropane with a carboxylic acid including 15 to 85 mole % of oleic acid based on the total carboxylic acid and 15 to 85 mole % of isostearic acid based on the total carboxylic acid, or a carboxylic acid obtained by incorporating into the carboxylic acid 85 mole % or less of monocarboxylic acid having 6 to 22 carbon atoms (excluding oleic acids and isostearic acids).
- the synthetic ester has a kinematic viscosity of 40 to 80 cSt (mm 2 /s) 40° C. and a
- U.S. Pat. No. 6,402,983 teaches a flame retardant hydraulic oil containing a partial ester of a polyol and a monocarboxylic acid.
- the polyol partial ester is formed by reacting a polyol having a total of 6 to 22 carbon atoms and a total of 3 to 6 hydroxyl groups with an acyclic monocarboxylic acid having a total of 6 to 22 carbon atoms, said polyol partial ester having a hydroxyl value of 35 mg KOH/g or more, a flash point of 290° C. or higher and an average molecular weight of 600 to 1500.
- U.S. Pat. No. 4,519,932 teaches a low temperature, flame retardant hydraulic fluid comprising a blend of a 2 cSt oligomer of alpha olefins with mono- or di-esters and a polymethacrylate viscosity index improver.
- the oligomers of alpha olefins are dimers, trimers, tetramers, etc., of; e.g., decene.
- the oligomer used in the examples of this patent is the dimmer.
- the dimer is hydrogenated so that it is essentially fully saturated.
- the 2 cSt dimer is apparently specified to distinguish over U.S. Pat. No. 4,175,046 which teaches a combination of higher viscosity PAO plus dicarboxylic acid esters as engine oils.
- the fluid exhibits enhanced fire resistance, Table, column 7, lines 15-25.
- MIL-PRF-83282 is a synthetic hydrogenated PAO-based hydraulic fluid exhibiting fire resistance.
- the object of the paper is to trace the development of a lower pour point MIL-PRF-83282 fluid. At page 486 it is indicated that such a fluid would be based on synthetic PAO or a fluid similar to PAO which have been found to be better than MIL-PRF-5606 (which is a mineral oil-based lubricant).
- PAO fluids decene dimer and dimer/trimer blend
- the fluids all contained antioxidant and TAP.
- the dimer/trimer blend contained diisooctyl adipate (Fluid I) while the dimer only fluid contained dibutoxyethyl glutarate (Fluid II).
- the present invention is directed to a functional fluid, especially a hydraulic fluid, exhibiting excellent low flammability properties (i.e., flame retardant properties) and excellent low temperature viscometrics comprising as essential elements a hydrocarbon oil base oil derived from a Gas-to-Liquids process, preferably a Fischer-Tropsch process, most preferably hydrodewaxed or hydroisomerized/catalytic (and/or solvent) dewaxed Fischer-Tropsch wax, optionally a minor quantity (up to 50 wt % of the base oil) of polyalphaolefin, a dicarboxylic acid ester, a pour point depressant and triaryl phosphate.
- a hydrocarbon oil base oil derived from a Gas-to-Liquids process, preferably a Fischer-Tropsch process, most preferably hydrodewaxed or hydroisomerized/catalytic (and/or solvent) dewaxed Fischer-Tropsch wax, optionally a minor quantity (up to 50
- the base oil comprises from about 65 wt % to about 90 wt % of the formulated composition.
- the dicarboxylic acid ester comprises about 5 to about 30 wt % of the formulated composition.
- the triaryl phosphate comprises about 0.5 to about 5 wt %, preferably about 1 to about 3 wt %, of the formulated composition.
- the pour point depressant comprises about 0.05 to 5.0 wt % of the formulated composition.
- the base oil is a hydrocarbon oil derived from a Gas-to-Liquids (GTL) process material.
- GTL Gas-to-Liquids
- GTL materials are materials that are derived via one or more synthesis, combination, transformation, rearrangement, and/or degradation/deconstructive processes from gaseous carbon-containing compounds, hydrogen-containing compounds and/or elements as feedstocks such as hydrogen, carbon dioxide, carbon monoxide, water, methane, ethane, ethylene, acetylene, propane, propylene, propyne, butane, butylenes, and butynes.
- GTL base stocks and/or base oils are GTL materials of lubricating viscosity that are generally derived from hydrocarbons, for example waxy synthesized hydrocarbons, that are themselves derived from simpler gaseous carbon-containing compounds, hydrogen-containing compounds and/or elements as feedstocks, typically CO and H 2 synthesis gas.
- GTL base stocks and/or base oil(s) include: (1) oils boiling in the lube oil boiling range separated/fractionated from synthesized GTL materials, such as, for example, by distillation and subsequent subjection to a final wax processing step which involves either or both of a catalytic dewaxing process, or a solvent dewaxing process, to produce lube oils of reduced/low pour point; (2) synthesized wax isomerates, comprising, for example, oils produced by hydrodewaxing or hydroisomerization, followed by cat and/or solvent dewaxing of synthesized wax or synthesized waxy hydrocarbons; (3) hydrodewaxing or hydroisomerization followed by cat and/or solvent dewaxing of Fischer-Tropsch (F-T) material (i.e., hydrocarbons, waxy hydrocarbons, waxes and possible analogous oxygenates, which are themselves synthesized from synthesis gas comprising CO and hydrogen); preferably oils produced by hydrodewaxing or hydroisomerization
- GTL base stock(s) and/or base oil(s) derived from GTL materials are characterized typically as having kinematic viscosities at 100° C. of from about 2 mm 2 /s to about 50 mm 2 /s (ASTM D445). They are further characterized typically as having pour points of about ⁇ 5° C. to about ⁇ 40° C. (ASTM D97). They are also characterized typically as having viscosity indices of about 80 to 140 or greater (ASTM D2270).
- the base stock/base oil derived from GTL process materials used to produce the flame retardant functional fluid has a kinematic viscosity at 100° C. in the range of from about 3.5 mm 2 /s to about 10 mm 2 /s, preferably about 3.5 mm 2 /s to about 6 mm 2 /s, more preferably about 3.5 mm 2 /s to about 4 mm 2 /s.
- the GTL fluids employed in the present invention having kinematic viscosities at 100° C. in the range of about 3.5 mm 2 /s to 10 mm 2 /s have pour points in the range of from about ⁇ 15 to about ⁇ 30° C.
- the GTL fluids generally have pour points interior to those exhibited by PAO fluids of similar kinematic viscosities.
- the GTL base stock(s) and/or base oil(s) are typically highly paraffinic (>90% saturates), and may contain mixtures of monocycloparaffins and multicycloparaffins in combination with non-cyclic isoparaffins.
- the ratio of the naphthenic (i.e., cycloparaffin) content in such combinations varies with the catalyst and temperature used.
- GTL base stock(s) and/or base oil(s) typically have a very low sulfur and nitrogen content, generally containing less than about 10 ppm, and more typically less than about 5 ppm of each of these elements.
- the sulfur and nitrogen content of GTL base stock(s) and/or base oil(s) obtained from F-T material, especially F-T wax, is essentially nil.
- GTL base stock and/or base oil is to be understood as embracing individual fractions of such materials of wide viscosity range as recovered in the production process, mixtures of two or more of such fractions, as well as mixtures of one or two or more low viscosity fractions with one, two or more higher viscosity fractions to produce a blend wherein the blend exhibits a target kinematic viscosity.
- Dicarboxylic acid esters useful in this invention are prepared from the esterification of the dicarboxylic acid with excess of alcohol.
- the esterification reaction is well known in the art.
- Suitable dicarboxylic acids include but are not limited to succinic acid, maleic acid, adipic acid, azealic acid, suberic acid, phthalic acid, sebacic acid, linoleic acid.
- Suitable alcohols include but are not limited to butyl alcohol, n-pentyl alcohol, iso-pentyl alcohol, n-hexyl alcohol, n-heptyl alcohol, n-octyl alcohol, isooctyl alcohol, 2-ethyl-hexyl alcohol, nonyl alcohol, isononyl alcohol, decyl alcohol, undecyl alcohol, dodecyl alcohol, tridecyl alcohol and the like.
- esters include dioctyl adipiate, di(2-ethylhexyl) sebacate, diisooctyl azealate, dioctyl sebacate, diisooctyl phthalate, diisononyl phthalate, diisodecyl adipiate, diisooctyl adipiate, diisononyl adipiate, diisodecyl suberate and the like.
- the preferred esters are diisodecyl adipiate, diisononyl adipiate and diisooctyl adipiate having a pour point (ASTM D97) of ⁇ 60° C. and lower.
- Anti-wear agents are also essential components of the present invention so as to comply with original equipment manufactures (OEM) and/or military and/or civilian end user specifications.
- Triaryl phosphates are the traditional anti-wear agents, tricresyl phosphates being the anti-wear additive of choice.
- the lubricants of the present invention contain a pour point depressant.
- pour point depressants also known as lube oil flow improvers
- Conventional pour point depressants are added in an amount in the range of about 0.05 to about 5 wt %, preferably about 0.05 to about 1.5 wt %, as active ingredient, based on the total weight of the lubricating oil formulation.
- Suitable pour point depressants include, without limitation, polyacrylates, polymethacrylates, polyarylamides, condensate products of haloparaffin waxes and aromatic compounds, vinyl carboxylate polymers and terpolymers of dialkyl furmarates, vinyl esters of fatty acids and alkyl vinyl ethers.
- Useful pour point depressants and/or their method of preparation are described in U.S. Pat. No. 1,815,022; U.S. Pat. No. 2,015,748; U.S. Pat. No. 2,191,498; U.S. Pat. No. 2,387,501; U.S. Pat. No. 2,655,479; U.S. Pat. No. 2,666,746; U.S. Pat. No. 2,721,877; U.S. Pat. No. 2,721,878, U.S. Pat. No. 3,250,715.
- Preferred pour point depressants are the polyacrylates and polymethacrylates.
- the formulations of the present invention may further contain up to about 50 wt %, preferably up to 40 wt %, more preferably up to 30 wt % poly alpha olefin having kinematic viscosities at 100° C. in the range of about 2 to 10 mm 2 /s, preferably about 2 to 6 mm 2 /s, more preferably about 2 to 4 mm 2 /s.
- the fluids contain a base oil consisting solely of GTL base oil.
- hydraulic fluids comprising a Group III base oil specifically GTL fluids obtained by the hydrodewaxing or hydroisomerization/catalytic (and/or solvent) dewaxing of Fischer-Tropsch wax (hereinafter collectively identified as and referred to as GTL fluids), in combination with decarboxylic acid and a pour point depressant exhibits significantly improved low flammability properties (i.e., exhibit flame retardant properties) as compared to hydraulic fluids based on mineral oils, as exemplified by hydraulic fluids meeting MIL-PRF 5606 specifications. Such fluids also unexpectedly exhibit superior flame retardant properties as compared to other Group III base oil-based hydraulic fluids.
- GTL fluids Fischer-Tropsch wax
- the present formulation not only has similar flame retardant properties as do the PAO-based hydraulic fluids but also meet the low temperature viscometric property requirements of such PAO-based hydraulic fluids as specified in MIL-PRF 83282, a pour point of ⁇ 55° C. maximum.
- the fluids of the present invention exhibit flame propagation rates of about 2 mm/s or less, preferably about 1.8 mm/s or less, more preferably about 1.7 mm/s or less.
- the base oils were used to prepare formulated hydraulic fluids as described in Table 2, which recites the viscometric properties of the formulated fluids and compares the fluids to a mineral oil-based fluid meeting MIL-PRF-5606, as well as reporting the flame propagation rates of the fluids.
- the dicarboxylic acid ester used in this example was diisodecyl adipate which has a KV at 100° C. of 3.68 mm 2 /s at 20° C. of about 25 mm 2 /s and at ⁇ 40° C. of about 3,450 mm 2 /s and a pour point of ⁇ 60° C.
- the pour point depressant was an alkylated fumarate/vinyl acetate copolymer, on an as-received basis.
- the hydraulic fluids made using GTL have very low pour points as compared to Fluid 4, a fluid made using a different Group III-type base oil and containing the same additives as invention Fluids 2 and 3.
- Fluid 4 made using a different Group III-type base stock even when additized with a pour point depressant, could not meet the ⁇ 55° C. maximum pour point specification set for the hydraulic fluid.
- Fluid 4 was solid at ⁇ 40° C. (i.e., at about pour point temperature). Fluid 4 failed to meet the pour point target despite being based on a Group III base stock and despite being additized with a pour point depressant.
- Fluid 1 had a pour point of ⁇ 65° C.
- the PAO base oil had an unadditized pour point of ⁇ 73° C.
- the additization of the PAO raised the pour point to ⁇ 65° C. from an unadditized pour point of ⁇ 73° C.
- the effect of additives is to raise the pour point.
- Fluids 2 and 3 have lower flame propagation rates than does the hydraulic fluids containing the same additives package but employing the Group III base oil Yubase4.
- the flame propagation rate of Fluids 2 and 3 is also significantly superior to that of the mineral oil-based fluid (MIL-PRF-5606).
- the formulations made using the GTL base exhibited flame propagation rates which are significantly superior, being 1.7 and 1.8 mm 2 /s, respectively. While 1.7 and 1.8 mm 2 /s may on their face appear substantially equivalent to 2.0 mm 2 /s, the difference is significant when it is taken into consideration that flame propagation is measured by ASTM D5306, and the standard derivation for measurements from the same lab for MIL-PRF-83282 (PAO-based hydraulic fluids) is 0.07 mm/s.
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Abstract
Lubricating oil compositions having low flammability properties and good low temperatures suitable for use as hydraulic fluids comprise a major amount of GTL base oil, optionally a minor amount of polyolphaolefins, an additive amount of about 5 to 30 wt % of dicarboxylic acid ester and minor amount of a pour-point depressant.
Description
- This Application claims the benefit of U.S. Provisional Application 61/123,926 filed Apr. 10, 2008, herein incorporated by reference.
- 1. Field of the Invention
- The present invention relates to hydraulic fluids exhibiting flame retardant properties and good low temperature viscometrics.
- 2. Description of the Related Art
- Functional fluids, especially hydraulic fluids exhibiting flame retardant properties, are known in the art. The fire-resistant/flame retardant hydraulic fluid market is currently divided into the following main classes:
- 1) HFA, which are high water content fluids, >80% water;
- 2) HFB, which are water-in-oil emulsions, <50% water;
- 3) HFC, which are water-glycol fluids, 30-80% water;
- 4) HFD-R, which are phosphate ester fluids; and
- 5) HFD-U, which are all other, including polyol ester-based fluids, vegetable oil ester-based fluids, fluorocarbon-based fluids, silicate ester-based fluids, silicone-based fluids and PAO-based fluids.
- Fire resistant/flame retardant fluids are described in the literature.
- U.S. Pat. No. 3,793,207 teaches fire-resistant hydraulic fluids having improved low temperature characteristics; e.g., viscosity, pour point, and cloud point which consist mainly of a mixture of a hydrocarbon base oil, preferably a synthetic hydrocarbon, a dialkyl carboxylate ester and an ortho-silicate. The synthetic hydrocarbon oil constitutes the base oil of the composition, the ester of a dicarboxylic acid constitutes 20-30 wt % of the composition, and the alkyl silicate constitutes 10-15 wt % of the composition, with small percentages of other functional additives being present, such as anti-wear agents, hydrolysis suppressants, anti-foamants, etc. The hydrocarbon oil employed has a viscosity of from 8,500 to 10,800 cs at −40° F., 25-35 cs at 100° F., and 4-8 cs at 210° F., and is preferably a dialkylaromatic hydrocarbon. The preferred ester of a dicarboxylic acid is a dialkyl adipate ester of a C6-C10 alcohol. The fluid is hydrolytically stable, has excellent low temperature viscometrics and has a high flash point, fire point and autogenous ignition temperature.
- U.S. Pat. No. 3,873,464 teaches a flame resistant hydraulic fluid comprising a major amount of a synthetic hydrocarbon oil having at least 30 carbon atoms in each molecule, and a small amount of a mixture comprising chlorinated polyphenyls and a trihydrocarbon phosphate. The synthetic hydrocarbon base oil is of the type made by polymerizing olefins in the presence of a suitable catalyst, such as BF3 or AlCl3. The preferred synthetic hydrocarbon oil is a trimer of decene.
- U.S. Pat. No. 6,361,711 teaches a flame retardant hydraulic oil containing a hydraulic base oil including as essential component a synthetic ester formed by reacting at least one polyol selected from the group consisting of neopentyl glycol, 2,2-dimethyl-3-hydroxy propyl-2′,2′-dimethyl-3′-hydroxypropionate, glycerine and trimethylolpropane with a carboxylic acid including 15 to 85 mole % of oleic acid based on the total carboxylic acid and 15 to 85 mole % of isostearic acid based on the total carboxylic acid, or a carboxylic acid obtained by incorporating into the carboxylic acid 85 mole % or less of monocarboxylic acid having 6 to 22 carbon atoms (excluding oleic acids and isostearic acids). The synthetic ester has a kinematic viscosity of 40 to 80 cSt (mm2/s) 40° C. and a flash point of 290° C. or higher.
- U.S. Pat. No. 6,402,983 teaches a flame retardant hydraulic oil containing a partial ester of a polyol and a monocarboxylic acid. The polyol partial ester is formed by reacting a polyol having a total of 6 to 22 carbon atoms and a total of 3 to 6 hydroxyl groups with an acyclic monocarboxylic acid having a total of 6 to 22 carbon atoms, said polyol partial ester having a hydroxyl value of 35 mg KOH/g or more, a flash point of 290° C. or higher and an average molecular weight of 600 to 1500.
- U.S. Pat. No. 4,519,932 teaches a low temperature, flame retardant hydraulic fluid comprising a blend of a 2 cSt oligomer of alpha olefins with mono- or di-esters and a polymethacrylate viscosity index improver. The oligomers of alpha olefins are dimers, trimers, tetramers, etc., of; e.g., decene. The oligomer used in the examples of this patent is the dimmer. The dimer is hydrogenated so that it is essentially fully saturated. The 2 cSt dimer is apparently specified to distinguish over U.S. Pat. No. 4,175,046 which teaches a combination of higher viscosity PAO plus dicarboxylic acid esters as engine oils. The fluid exhibits enhanced fire resistance, Table, column 7, lines 15-25.
- The paper “Development of a −54° C. to 135° C. Synthetic Hydrocarbon-based Fire Resistant Hydraulic Fluid” explores the development of a MIL-H-83282 fire resistant hydraulic fluid. MIL-PRF-83282 is a synthetic hydrogenated PAO-based hydraulic fluid exhibiting fire resistance. The object of the paper is to trace the development of a lower pour point MIL-PRF-83282 fluid. At page 486 it is indicated that such a fluid would be based on synthetic PAO or a fluid similar to PAO which have been found to be better than MIL-PRF-5606 (which is a mineral oil-based lubricant).
- The paper “Pump Evaluation of Hydrogenated Polyalphaolefin Candidates for a −54° C. to 135° C. Fire Resistant Air Force Aircraft Hydraulic Fluid” similarly addresses lower pour point MIL-PRF-83282 fluids. PAO fluids (decene dimer and dimer/trimer blend) are the base stocks. The fluids all contained antioxidant and TAP. The dimer/trimer blend contained diisooctyl adipate (Fluid I) while the dimer only fluid contained dibutoxyethyl glutarate (Fluid II).
- The present invention is directed to a functional fluid, especially a hydraulic fluid, exhibiting excellent low flammability properties (i.e., flame retardant properties) and excellent low temperature viscometrics comprising as essential elements a hydrocarbon oil base oil derived from a Gas-to-Liquids process, preferably a Fischer-Tropsch process, most preferably hydrodewaxed or hydroisomerized/catalytic (and/or solvent) dewaxed Fischer-Tropsch wax, optionally a minor quantity (up to 50 wt % of the base oil) of polyalphaolefin, a dicarboxylic acid ester, a pour point depressant and triaryl phosphate.
- The base oil comprises from about 65 wt % to about 90 wt % of the formulated composition.
- The dicarboxylic acid ester comprises about 5 to about 30 wt % of the formulated composition.
- The triaryl phosphate comprises about 0.5 to about 5 wt %, preferably about 1 to about 3 wt %, of the formulated composition.
- The pour point depressant comprises about 0.05 to 5.0 wt % of the formulated composition.
- The base oil is a hydrocarbon oil derived from a Gas-to-Liquids (GTL) process material.
- GTL materials are materials that are derived via one or more synthesis, combination, transformation, rearrangement, and/or degradation/deconstructive processes from gaseous carbon-containing compounds, hydrogen-containing compounds and/or elements as feedstocks such as hydrogen, carbon dioxide, carbon monoxide, water, methane, ethane, ethylene, acetylene, propane, propylene, propyne, butane, butylenes, and butynes. GTL base stocks and/or base oils are GTL materials of lubricating viscosity that are generally derived from hydrocarbons, for example waxy synthesized hydrocarbons, that are themselves derived from simpler gaseous carbon-containing compounds, hydrogen-containing compounds and/or elements as feedstocks, typically CO and H2 synthesis gas. GTL base stocks and/or base oil(s) include: (1) oils boiling in the lube oil boiling range separated/fractionated from synthesized GTL materials, such as, for example, by distillation and subsequent subjection to a final wax processing step which involves either or both of a catalytic dewaxing process, or a solvent dewaxing process, to produce lube oils of reduced/low pour point; (2) synthesized wax isomerates, comprising, for example, oils produced by hydrodewaxing or hydroisomerization, followed by cat and/or solvent dewaxing of synthesized wax or synthesized waxy hydrocarbons; (3) hydrodewaxing or hydroisomerization followed by cat and/or solvent dewaxing of Fischer-Tropsch (F-T) material (i.e., hydrocarbons, waxy hydrocarbons, waxes and possible analogous oxygenates, which are themselves synthesized from synthesis gas comprising CO and hydrogen); preferably oils produced by hydrodewaxing or hydroisomerization followed by cat and/or solvent dewaxing of F-T waxy hydrocarbons or of F-T waxes, or mixtures thereof.
- GTL base stock(s) and/or base oil(s) derived from GTL materials, especially hydrodewaxed or hydroisomerized followed by cat and/or solvent dewaxing dewaxed synthesized wax or synthesized waxy feed, preferably F-T material-derived base stock(s) and/or base oil(s), are characterized typically as having kinematic viscosities at 100° C. of from about 2 mm2/s to about 50 mm2/s (ASTM D445). They are further characterized typically as having pour points of about −5° C. to about −40° C. (ASTM D97). They are also characterized typically as having viscosity indices of about 80 to 140 or greater (ASTM D2270).
- For the purposes of the present invention the base stock/base oil derived from GTL process materials used to produce the flame retardant functional fluid has a kinematic viscosity at 100° C. in the range of from about 3.5 mm2/s to about 10 mm2/s, preferably about 3.5 mm2/s to about 6 mm2/s, more preferably about 3.5 mm2/s to about 4 mm2/s. The GTL fluids employed in the present invention having kinematic viscosities at 100° C. in the range of about 3.5 mm2/s to 10 mm2/s have pour points in the range of from about −15 to about −30° C. The GTL fluids generally have pour points interior to those exhibited by PAO fluids of similar kinematic viscosities.
- The GTL base stock(s) and/or base oil(s) are typically highly paraffinic (>90% saturates), and may contain mixtures of monocycloparaffins and multicycloparaffins in combination with non-cyclic isoparaffins. The ratio of the naphthenic (i.e., cycloparaffin) content in such combinations varies with the catalyst and temperature used. Further, GTL base stock(s) and/or base oil(s) typically have a very low sulfur and nitrogen content, generally containing less than about 10 ppm, and more typically less than about 5 ppm of each of these elements. The sulfur and nitrogen content of GTL base stock(s) and/or base oil(s) obtained from F-T material, especially F-T wax, is essentially nil.
- The term GTL base stock and/or base oil is to be understood as embracing individual fractions of such materials of wide viscosity range as recovered in the production process, mixtures of two or more of such fractions, as well as mixtures of one or two or more low viscosity fractions with one, two or more higher viscosity fractions to produce a blend wherein the blend exhibits a target kinematic viscosity.
- Dicarboxylic acid esters useful in this invention are prepared from the esterification of the dicarboxylic acid with excess of alcohol. The esterification reaction is well known in the art. Suitable dicarboxylic acids include but are not limited to succinic acid, maleic acid, adipic acid, azealic acid, suberic acid, phthalic acid, sebacic acid, linoleic acid. Suitable alcohols include but are not limited to butyl alcohol, n-pentyl alcohol, iso-pentyl alcohol, n-hexyl alcohol, n-heptyl alcohol, n-octyl alcohol, isooctyl alcohol, 2-ethyl-hexyl alcohol, nonyl alcohol, isononyl alcohol, decyl alcohol, undecyl alcohol, dodecyl alcohol, tridecyl alcohol and the like. Specific examples of these esters include dioctyl adipiate, di(2-ethylhexyl) sebacate, diisooctyl azealate, dioctyl sebacate, diisooctyl phthalate, diisononyl phthalate, diisodecyl adipiate, diisooctyl adipiate, diisononyl adipiate, diisodecyl suberate and the like. The preferred esters are diisodecyl adipiate, diisononyl adipiate and diisooctyl adipiate having a pour point (ASTM D97) of −60° C. and lower.
- Anti-wear agents are also essential components of the present invention so as to comply with original equipment manufactures (OEM) and/or military and/or civilian end user specifications. Triaryl phosphates are the traditional anti-wear agents, tricresyl phosphates being the anti-wear additive of choice.
- Because hydraulic fluids typically must also meet stringent low temperature viscometric properties, especially the −55° C. maximum pour point specification contained in MIL-PRF 83282, the lubricants of the present invention contain a pour point depressant.
- Conventional pour point depressants (also known as lube oil flow improvers) are added in an amount in the range of about 0.05 to about 5 wt %, preferably about 0.05 to about 1.5 wt %, as active ingredient, based on the total weight of the lubricating oil formulation.
- Suitable pour point depressants include, without limitation, polyacrylates, polymethacrylates, polyarylamides, condensate products of haloparaffin waxes and aromatic compounds, vinyl carboxylate polymers and terpolymers of dialkyl furmarates, vinyl esters of fatty acids and alkyl vinyl ethers. Useful pour point depressants and/or their method of preparation are described in U.S. Pat. No. 1,815,022; U.S. Pat. No. 2,015,748; U.S. Pat. No. 2,191,498; U.S. Pat. No. 2,387,501; U.S. Pat. No. 2,655,479; U.S. Pat. No. 2,666,746; U.S. Pat. No. 2,721,877; U.S. Pat. No. 2,721,878, U.S. Pat. No. 3,250,715.
- Preferred pour point depressants are the polyacrylates and polymethacrylates.
- The formulations of the present invention, optionally, may further contain up to about 50 wt %, preferably up to 40 wt %, more preferably up to 30 wt % poly alpha olefin having kinematic viscosities at 100° C. in the range of about 2 to 10 mm2/s, preferably about 2 to 6 mm2/s, more preferably about 2 to 4 mm2/s. Preferably the fluids contain a base oil consisting solely of GTL base oil.
- It has been discovered that hydraulic fluids comprising a Group III base oil specifically GTL fluids obtained by the hydrodewaxing or hydroisomerization/catalytic (and/or solvent) dewaxing of Fischer-Tropsch wax (hereinafter collectively identified as and referred to as GTL fluids), in combination with decarboxylic acid and a pour point depressant exhibits significantly improved low flammability properties (i.e., exhibit flame retardant properties) as compared to hydraulic fluids based on mineral oils, as exemplified by hydraulic fluids meeting MIL-PRF 5606 specifications. Such fluids also unexpectedly exhibit superior flame retardant properties as compared to other Group III base oil-based hydraulic fluids. Finally, despite the fact that the GTL fluids have higher inherent pour points than PAO, the present formulation not only has similar flame retardant properties as do the PAO-based hydraulic fluids but also meet the low temperature viscometric property requirements of such PAO-based hydraulic fluids as specified in MIL-PRF 83282, a pour point of −55° C. maximum.
- The fluids of the present invention exhibit flame propagation rates of about 2 mm/s or less, preferably about 1.8 mm/s or less, more preferably about 1.7 mm/s or less.
- Various fluids formulated using PAO, GTL, mixtures of PAO and GTL, and a Group III fluid identified as Yubase produced by the SK UCO Lube process (Korea) by hydrocracking fuel bottoms followed by catalytic wax isomerization, were compared against each other and against a mineral oil-based hydraulic fluid meeting the specification of MIL-PRF-5606.
- The specifications of the PAO4, GTL4 and Yubase4 base oils are given in Table 1.
-
TABLE 1 Properties of the Base Oils Base Oil Test PAO4 GTL4 Yubase4 KV @ 40° C., mm2/s ASTM D445 16.8 14.7 19.7 KV @ 100° C., mm2/s ASTM D445 3.9 3.6 4.2 Pour Point, ° C. ASTM D97 −73 −27 −15 AMW — 438 300 300 - These base oils were used to prepare formulated hydraulic fluids as described in Table 2, which recites the viscometric properties of the formulated fluids and compares the fluids to a mineral oil-based fluid meeting MIL-PRF-5606, as well as reporting the flame propagation rates of the fluids. The dicarboxylic acid ester used in this example was diisodecyl adipate which has a KV at 100° C. of 3.68 mm2/s at 20° C. of about 25 mm2/s and at −40° C. of about 3,450 mm2/s and a pour point of −60° C. The pour point depressant was an alkylated fumarate/vinyl acetate copolymer, on an as-received basis.
-
TABLE 2 MIL-PRF- Fluid 3 5606 Fluid 1 Fluid 2 GTL/ Fluid 4 Mineral Oil PAO GTL PAO Group III wt % wt % wt % wt % wt % Base Oil Naphthenic Base 85.7 0 0 0 0 Oil GTL 3.6 0 0 76.7 38.4 0 Group III-4 0 0 0 0 76.7 PAO 4 0 77.0 0 38.4 0 Dicarboxylic 0 20.0 20.0 20.0 20.0 Acid Ester PPD 0 0 0.3 0.2 0.3 VI Improver 13.6 0 0 0 0 Balance 0.7 3.0 3.0 3.0 3.0 Additives Properties KV @ −40° C., 469 2634 4328 3148 solid mm2/s KV @ 40° C., 13.4 16.11 14.08 15.04 18.44 mm2/s KV @ 100° C., 5.2 3.78 3.57 3.67 4.12 mm2/s VI (Calc.) 400 126 140 133 127 Pour Point, ° C. −65 <−60 −57 <−63 −42 Flash Point, ° C. ASTM D92 222 217 — 224 Fire Point, ° C. ASTM D92 258 253 256 AIT, ° C. ASTM E659 338 324/340 — 344 Flame 10 1.5 1.7 1.8 2.0 Propagation, mm/2 - As seen by reference to Table 2 above, the hydraulic fluids made using GTL (Fluids 2 and 3, fluids of the present invention) have very low pour points as compared to Fluid 4, a fluid made using a different Group III-type base oil and containing the same additives as invention Fluids 2 and 3. Fluid 4, made using a different Group III-type base stock, even when additized with a pour point depressant, could not meet the −55° C. maximum pour point specification set for the hydraulic fluid. Fluid 4 was solid at −40° C. (i.e., at about pour point temperature). Fluid 4 failed to meet the pour point target despite being based on a Group III base stock and despite being additized with a pour point depressant.
- While both invention Fluids 2 and 3 met or exceeded the pour point target of −55° C., as did Fluid 1 (PAO-based fluid of the prior art), it must be recognized that the pour point of the unadditized PAO was −73° C. whereas the pour point of the unadditized GTL was −27° C.
- Thus, while Fluid 1 (PAO) had a pour point of −65° C., this is not totally unexpected in view of the fact that the PAO base oil had an unadditized pour point of −73° C. The additization of the PAO raised the pour point to −65° C. from an unadditized pour point of −73° C. Thus, the effect of additives is to raise the pour point.
- What is unexpected, however, is that the GTL Group III base stock having an unadditized pour point of −27° C. produced a fluid (Fluid 2) having an additized pour point of −57° C. with only 0.3 wt % pour point depressant, whereas Fluid 4 based on Yubase Group III base oil having an inherent pour point of −15° C. had an additized pour point of only −42° C. and is reported as solid at −40° C., at the same pour point depressant treat rate.
- Thus, it is unexpected that a hydraulic fluid meeting the pour point target of −55° C. maximum could be formulated using the GTL base oil, even when additized with a pour point depressant.
- Further review of the data in Table 2 shows that fluids of the invention (Fluids 2 and 3) have lower flame propagation rates than does the hydraulic fluids containing the same additives package but employing the Group III base oil Yubase4. The flame propagation rate of Fluids 2 and 3 is also significantly superior to that of the mineral oil-based fluid (MIL-PRF-5606).
- Based on the flame propagation results obtained for the Group III Yubase base oil formulation (Fluid 2), 2 mm2/s, the formulations made using the GTL base exhibited flame propagation rates which are significantly superior, being 1.7 and 1.8 mm2/s, respectively. While 1.7 and 1.8 mm2/s may on their face appear substantially equivalent to 2.0 mm2/s, the difference is significant when it is taken into consideration that flame propagation is measured by ASTM D5306, and the standard derivation for measurements from the same lab for MIL-PRF-83282 (PAO-based hydraulic fluids) is 0.07 mm/s.
Claims (4)
1. A flame retardant hydraulic fluid comprising a base oil consisting of GTL base oil and optionally up to 50 wt % PAO, from about 5 to about 30 wt % dicarboxylic acid based on the total weight of the fluid, from about 0.5 to about 5 wt % of a pour point depressant based on the total weight of the fluid, wherein the GTL base oil has a kinematic viscosity at 100° C. in the range of about 2 mm2/s to 10 mm2/s and a pour point of about −30° C. or higher, the hydraulic fluid having a pour point of −55° C. maximum.
2. The flame retardant hydraulic fluid of claim 1 wherein the base oil consists of GTL base oil and optionally up to 40 wt % PAO.
3. The flame retardant hydraulic fluid of claim 1 wherein the base oil consists entirely of GTL base oil.
4. The flame retardant hydraulic fluid of claim 1 , 2 or 3 wherein the hydraulic fluid exhibits a flame propagation rate of about 2 mm2/s or less by ASTM D5307.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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US12/383,407 US20090286705A1 (en) | 2008-04-10 | 2009-03-24 | Flame retardant lubricating oil compositions |
PCT/US2009/002202 WO2009126276A1 (en) | 2008-04-10 | 2009-04-08 | Flame retardant lubricating oil compositions |
CA2720070A CA2720070A1 (en) | 2008-04-10 | 2009-04-08 | Flame retardant lubricating oil compositions |
EP09729910A EP2262876A4 (en) | 2008-04-10 | 2009-04-08 | Flame retardant lubricating oil compositions |
Applications Claiming Priority (2)
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US12362608P | 2008-04-10 | 2008-04-10 | |
US12/383,407 US20090286705A1 (en) | 2008-04-10 | 2009-03-24 | Flame retardant lubricating oil compositions |
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US20090286705A1 true US20090286705A1 (en) | 2009-11-19 |
Family
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US12/383,407 Abandoned US20090286705A1 (en) | 2008-04-10 | 2009-03-24 | Flame retardant lubricating oil compositions |
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US (1) | US20090286705A1 (en) |
EP (1) | EP2262876A4 (en) |
CA (1) | CA2720070A1 (en) |
WO (1) | WO2009126276A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2565257A4 (en) * | 2010-04-27 | 2013-10-16 | Hannal Inc | Fire-resistant hydraulic oil |
JP2015028160A (en) * | 2013-06-28 | 2015-02-12 | Jx日鉱日石エネルギー株式会社 | Compressor oil |
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US3793207A (en) * | 1971-11-05 | 1974-02-19 | Chevron Res | Fire-resistant hydraulic fluid |
US3873464A (en) * | 1970-12-28 | 1975-03-25 | Mobil Oil Corp | Flame resistant hydraulic fluid |
US4370281A (en) * | 1978-07-21 | 1983-01-25 | Ciba-Geigy Ag | Triaryl phosphates |
US4519932A (en) * | 1982-09-20 | 1985-05-28 | National Distillers And Chemical Corporation | Low temperature hydraulic fluids based on two centistoke synthetic hydrocarbons |
US6361711B1 (en) * | 1992-12-07 | 2002-03-26 | Idemitsu Kosan Co., Ltd. | Flame retardant hydraulic oil containing a synthetic ester formed by reaction of a polyol and a mixture of carboxylic acids including oleic acid and isostearic acid |
US6402983B1 (en) * | 1992-12-07 | 2002-06-11 | Idemitsu Kosan Co., Ltd. | Flame retardant hydraulic oil containing a partial ester of a polyol and a monocarboxylic acid |
US6534454B1 (en) * | 2000-06-28 | 2003-03-18 | Renewable Lubricants, Inc. | Biodegradable vegetable oil compositions |
US20040242436A1 (en) * | 2003-05-12 | 2004-12-02 | Southwest Research Institute | High octane lubricants for knock mitigation in flame propagation engines |
US20070066495A1 (en) * | 2005-09-21 | 2007-03-22 | Ian Macpherson | Lubricant compositions including gas to liquid base oils |
Family Cites Families (1)
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US7863229B2 (en) * | 2006-06-23 | 2011-01-04 | Exxonmobil Research And Engineering Company | Lubricating compositions |
-
2009
- 2009-03-24 US US12/383,407 patent/US20090286705A1/en not_active Abandoned
- 2009-04-08 EP EP09729910A patent/EP2262876A4/en not_active Withdrawn
- 2009-04-08 WO PCT/US2009/002202 patent/WO2009126276A1/en active Application Filing
- 2009-04-08 CA CA2720070A patent/CA2720070A1/en not_active Abandoned
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3873464A (en) * | 1970-12-28 | 1975-03-25 | Mobil Oil Corp | Flame resistant hydraulic fluid |
US3793207A (en) * | 1971-11-05 | 1974-02-19 | Chevron Res | Fire-resistant hydraulic fluid |
US4370281A (en) * | 1978-07-21 | 1983-01-25 | Ciba-Geigy Ag | Triaryl phosphates |
US4519932A (en) * | 1982-09-20 | 1985-05-28 | National Distillers And Chemical Corporation | Low temperature hydraulic fluids based on two centistoke synthetic hydrocarbons |
US6361711B1 (en) * | 1992-12-07 | 2002-03-26 | Idemitsu Kosan Co., Ltd. | Flame retardant hydraulic oil containing a synthetic ester formed by reaction of a polyol and a mixture of carboxylic acids including oleic acid and isostearic acid |
US6402983B1 (en) * | 1992-12-07 | 2002-06-11 | Idemitsu Kosan Co., Ltd. | Flame retardant hydraulic oil containing a partial ester of a polyol and a monocarboxylic acid |
US6534454B1 (en) * | 2000-06-28 | 2003-03-18 | Renewable Lubricants, Inc. | Biodegradable vegetable oil compositions |
US20040242436A1 (en) * | 2003-05-12 | 2004-12-02 | Southwest Research Institute | High octane lubricants for knock mitigation in flame propagation engines |
US20070066495A1 (en) * | 2005-09-21 | 2007-03-22 | Ian Macpherson | Lubricant compositions including gas to liquid base oils |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2565257A4 (en) * | 2010-04-27 | 2013-10-16 | Hannal Inc | Fire-resistant hydraulic oil |
JP2015028160A (en) * | 2013-06-28 | 2015-02-12 | Jx日鉱日石エネルギー株式会社 | Compressor oil |
Also Published As
Publication number | Publication date |
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EP2262876A4 (en) | 2011-11-30 |
WO2009126276A1 (en) | 2009-10-15 |
CA2720070A1 (en) | 2009-10-15 |
EP2262876A1 (en) | 2010-12-22 |
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