GB2430681A - Fischer-Tropsch lubricant base oil - Google Patents
Fischer-Tropsch lubricant base oil Download PDFInfo
- Publication number
- GB2430681A GB2430681A GB0625619A GB0625619A GB2430681A GB 2430681 A GB2430681 A GB 2430681A GB 0625619 A GB0625619 A GB 0625619A GB 0625619 A GB0625619 A GB 0625619A GB 2430681 A GB2430681 A GB 2430681A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fischer
- tropsch
- lubricating base
- base oil
- cst
- 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.)
- Granted
Links
- 239000002199 base oil Substances 0.000 title claims abstract description 175
- 239000000314 lubricant Substances 0.000 title claims description 43
- 230000001050 lubricating effect Effects 0.000 claims abstract description 137
- 239000000203 mixture Substances 0.000 claims abstract description 97
- 238000000034 method Methods 0.000 claims description 46
- 238000009835 boiling Methods 0.000 claims description 34
- 230000008569 process Effects 0.000 claims description 34
- 150000001336 alkenes Chemical class 0.000 claims description 24
- 239000010705 motor oil Substances 0.000 claims description 24
- 229930195733 hydrocarbon Natural products 0.000 claims description 19
- 150000002430 hydrocarbons Chemical class 0.000 claims description 19
- 238000002156 mixing Methods 0.000 claims description 16
- 239000000654 additive Substances 0.000 claims description 13
- 238000009826 distribution Methods 0.000 claims description 12
- 238000004227 thermal cracking Methods 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- 238000004458 analytical method Methods 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 230000018044 dehydration Effects 0.000 claims description 2
- 238000006297 dehydration reaction Methods 0.000 claims description 2
- 230000003606 oligomerizing effect Effects 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 description 44
- 239000000047 product Substances 0.000 description 36
- 239000003921 oil Substances 0.000 description 32
- 238000005336 cracking Methods 0.000 description 16
- 229910052751 metal Inorganic materials 0.000 description 16
- 239000002184 metal Substances 0.000 description 16
- 239000000463 material Substances 0.000 description 15
- 238000006384 oligomerization reaction Methods 0.000 description 15
- 239000002808 molecular sieve Substances 0.000 description 14
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 14
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000003208 petroleum Substances 0.000 description 12
- 230000007935 neutral effect Effects 0.000 description 11
- 239000001993 wax Substances 0.000 description 11
- 239000002904 solvent Substances 0.000 description 10
- 238000003786 synthesis reaction Methods 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 9
- 238000004517 catalytic hydrocracking Methods 0.000 description 9
- 239000012530 fluid Substances 0.000 description 9
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 9
- 239000010457 zeolite Substances 0.000 description 9
- 229910017052 cobalt Inorganic materials 0.000 description 8
- 239000010941 cobalt Substances 0.000 description 8
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 8
- -1 demulsifiers Substances 0.000 description 8
- 229910052697 platinum Inorganic materials 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 238000006317 isomerization reaction Methods 0.000 description 7
- 150000002739 metals Chemical class 0.000 description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 7
- 239000011148 porous material Substances 0.000 description 7
- 238000000197 pyrolysis Methods 0.000 description 7
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 6
- 229910021536 Zeolite Inorganic materials 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 6
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 6
- 239000010687 lubricating oil Substances 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 6
- 229910000510 noble metal Inorganic materials 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 5
- 230000005540 biological transmission Effects 0.000 description 5
- 238000005984 hydrogenation reaction Methods 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- 229910052763 palladium Inorganic materials 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000005194 fractionation Methods 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000395 magnesium oxide Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 238000005292 vacuum distillation Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 238000012935 Averaging Methods 0.000 description 3
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000002608 ionic liquid Substances 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000011733 molybdenum Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229910052702 rhenium Inorganic materials 0.000 description 3
- 229910052707 ruthenium Inorganic materials 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229910052723 transition metal Inorganic materials 0.000 description 3
- 150000003624 transition metals Chemical class 0.000 description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 3
- 229910052721 tungsten Inorganic materials 0.000 description 3
- 239000010937 tungsten Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000007866 anti-wear additive Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000004939 coking Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000003502 gasoline Substances 0.000 description 2
- 239000010720 hydraulic oil Substances 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- DDTIGTPWGISMKL-UHFFFAOYSA-N molybdenum nickel Chemical compound [Ni].[Mo] DDTIGTPWGISMKL-UHFFFAOYSA-N 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920013639 polyalphaolefin Polymers 0.000 description 2
- 229920013636 polyphenyl ether polymer Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- 102100036563 26S proteasome regulatory subunit 8 Human genes 0.000 description 1
- 108700036240 26S proteasome regulatory subunit 8 Proteins 0.000 description 1
- TVEXGJYMHHTVKP-UHFFFAOYSA-N 6-oxabicyclo[3.2.1]oct-3-en-7-one Chemical compound C1C2C(=O)OC1C=CC2 TVEXGJYMHHTVKP-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 101001053395 Arabidopsis thaliana Acid beta-fructofuranosidase 4, vacuolar Proteins 0.000 description 1
- 239000007848 Bronsted acid Substances 0.000 description 1
- 241001432959 Chernes Species 0.000 description 1
- 101100409512 Dictyostelium discoideum psmC5 gene Proteins 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 229910052776 Thorium Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- 101100521047 Xenopus laevis psmc3-b gene Proteins 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000011959 amorphous silica alumina Substances 0.000 description 1
- 230000003254 anti-foaming effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- UNYSKUBLZGJSLV-UHFFFAOYSA-L calcium;1,3,5,2,4,6$l^{2}-trioxadisilaluminane 2,4-dioxide;dihydroxide;hexahydrate Chemical compound O.O.O.O.O.O.[OH-].[OH-].[Ca+2].O=[Si]1O[Al]O[Si](=O)O1.O=[Si]1O[Al]O[Si](=O)O1 UNYSKUBLZGJSLV-UHFFFAOYSA-L 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910052676 chabazite Inorganic materials 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000006477 desulfuration reaction Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052675 erionite Inorganic materials 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum oxide Inorganic materials [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- CLDVQCMGOSGNIW-UHFFFAOYSA-N nickel tin Chemical compound [Ni].[Sn] CLDVQCMGOSGNIW-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000003870 refractory metal Substances 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003930 superacid Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G50/00—Production of liquid hydrocarbon mixtures from lower carbon number hydrocarbons, e.g. by oligomerisation
- C10G50/02—Production of liquid hydrocarbon mixtures from lower carbon number hydrocarbons, e.g. by oligomerisation of hydrocarbon oils for lubricating purposes
-
- 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
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/02—Well-defined hydrocarbons
- C10M105/04—Well-defined hydrocarbons aliphatic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
- C10G2/30—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
- C10G2/32—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G9/00—Thermal non-catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
-
- 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
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/02—Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1022—Fischer-Tropsch products
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/201—Impurities
- C10G2300/202—Heteroatoms content, i.e. S, N, O, P
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/30—Physical properties of feedstocks or products
- C10G2300/301—Boiling range
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/30—Physical properties of feedstocks or products
- C10G2300/302—Viscosity
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/80—Additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/10—Lubricating oil
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
- C10M2203/1085—Residual fractions, e.g. bright stocks 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
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/02—Viscosity; Viscosity index
-
- 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
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/085—Non-volatile compounds
-
- 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
-
- 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
- C10N2030/74—Noack Volatility
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Lubricants (AREA)
Abstract
A Fischer-Tropsch (FT) lubricating base oil blend comprising a FT distillate fraction and a FT bottoms fraction, characterised in that the blend: <UL ST="-"> <LI>has a kinematic viscosity between 3 and 10 cSt at 100{C <LI>a TGA Noack volatility & 45 wt % <LI>the kinematic viscosity of the distillate fraction is / 2 and & 3 </UL> and wherein the FT distillate fraction is the only distillate fraction blended into the base oil blend.
Description
1 BLENDING OF LOW VISCOSITY 2 FISCHER-TROPSCH BASE OILS AND 3
FISCHER-TROPSCH DERIVED BOTTOMS OR BRIGHT STOCK
4 5 CROSS REFERENCE TO RELATED APPLICATIONS
7 This application is related to co-pending U.S. Patent Application Serial 8 No. 10/235,150 flIed September 4, 2002, titled "Blending of Low Viscosity 9 Fischer-Tropsch Base Oils to Produce High Quality Lubricating Base Oils" and U.S. Patent Application Serial No. 10/301,391 filed November 20, 2002, 11 titled "Blending of Low Viscosity Fischer-Tropsch Base Oils With Conventional 12 Base Oils to Produce High Quality Lubricating Base Oils".
14 FIELD OF THE INVENTION
16 The invention relates to the blending of a low viscosity FischerTropsch 17 derived base oil fraction with a higher viscosity Fischer-Tropsch derived 18 bottoms fraction to produce a high quality lubricating base oil that is useful for 19 preparing commercial finished lubricants such as in crankcase engine oils.
21 BACKGROUND OF THE INVENTION
23 Finished lubricants and greases used for various applications, including 24 automobiles, diesel engines, natural gas engines, axles, transmissions, and industrial applications consist of two general components, a lubricating base 26 oil and additives. Lubricating base oil is the major constituent in these finished 27 lubricants and contributes significantly to the properties of the finished 28 lubricart. In general, a few lubricating base oils are used to manufacture a 29 wide variety of finished lubricants by varying the mixtures of individual lubricating base oils and indMdual additives.
32 Numerous governing organizations, including original equipment 33 manufacturers (OEM's), the American Petroleum institute (API), 1 Association des Consructeurs d' Automobiles (ACEA), 2 the American Society of Testing and Materials (ASTM), 3 the Society of Automotive Engineers (SAE), and 4 National Lubricating Grease Institute (NLGI) among others, define the specifications for lubricating base oils and finished lubricants. Increasingly, the 6 specifications for finished lubricants are calling for products with excellent 7 low temperature properties, high oxidation stability, and low volatility.
8 Currently only a small fraction of the base oils manufactured today are able to 9 meet the demanding specifications of premium lubricant products.
11 Syncrudes prepared from the Fischer-Tropsch process comprise a mixture of 12 various solid, liquid, and gaseous hydrocarbons. Those Fischer-Tropsch 13 products which boil within the range of lubricating base oil contain a 14 high proportion of wax which makes them ideal candidates for processing into lubricating base oil stocks. Accordingly, the hydrocarbon products recovered 16 from the Fischer-Tropsch process have been proposed as feedstocks for 17 preparing high quality lubricating base oils. When the Fischer-Tropsch waxes 18 are converted into Fischer-Tropsch base oils by various processes, such as 19 hydroprocessing and distillation, the base oils produced usually fall into different narrow-cut viscosity ranges. Typically, the kinematic viscosity of the 21 various cuts will range between 2.1 cSt and 12 cSt at 100 degrees C. Since 22 the kinematic viscosity of lubricating base oils typically will fall within the range 23 of from 3 to 32 cSt at 100 degrees C, the base oils that fall outside of this 24 viscosity range have limited use and, consequently, have less market value for engine oils.
27 The Fischer-Tropsch process typically produces a syncrude mixture 28 containing a wide range of products having varying molecular weights but with 29 a relatively high proportion of the products characterized by a low molecular weight and viscosity. Used by itself, this low viscosity product is not suitable 31 for many lubricant applications, especially high volume applications, such as 32 for engine oil. Currently, those Fischer-Tropsch derived base oils having 33 kinematic viscosities below 3 cSt at 100 degrees C have a limited market and I are usually cracked into lower molecular weight material, such as diesel and 2 naphtha. However, diesel and naphtha have a tower market value than 3 lubricating base oil. It would be desirable to be able to upgrade these low 4 viscosity base oils into products suitable for use as a lubricating base oil.
6 Conventional base oils prepared from petroleum derived feedstocks having a 7 kinematic viscosity below 3 cSt at 100 degrees C have a tow viscosity 8 index (VI) and high volatility. Consequently, low viscosity conventional base 9 oils are unsuitable for blending with higher viscosity conventional base oils because the blend will fail to meet the VI and volatility specifications for many 11 finished lubricants. Surprisingly, it has been found that Fischer- Tropsch 12 derived base oils having a kinematic viscosity above 2 and below 3 cSt at 13 100 degrees C display unusually high VI's, resulting in excellent low 14 temperature properties and volatilities similar to those seen in conventional Group I and Group II light neutral base oils which have a kinematic viscosity 16 generally fatling in the range of between 3.8 arid 4.7 cSt at 100 degrees C. 17 Even more surprising was that when the low viscosity Fischer-Tropsch 18 derived base oils were blended with certain Fischer-Tropsch derived bottom 19 fractions or bright stock, a VI premium was observed, i.e., the VI of the blend was significantly higher than would have been expected from a mere 21 averaging of the VI's for the two fractions. Consequently, it is has been 22 discovered that the low viscosity Fischer-Tropsch base oils fractions may be 23 advantageously employed as blending stock to prepare premium lubricants.
While Fischer-Tropsch derived lubricating base oil blends have been 26 described in the prior art, the method used to prepare them and the properties 27 of the prior art blends differ from the present invention. See, for example, 28 U.S. Patent Nos. 6,332,974; 6,096,940; 4,812,246; and 4,906,350. It has not 29 been previously taught that Fischer-Tropsch fractions having a viscosity of less than 3 cSt at 100 degrees C could be used to prepare lubricating 31 base oils suitable for blending finished lubricants meeting the specifications 32 for SAE Grade lOW, and 15W multigrade engine oils; monograde engine oils, 1 automatic transmission fluids; and ISO Viscosity Grade 22, 32, and 2 46 industrial oils. With the present invention, this becomes possible.
4 When referring to conventional lubricating base oils this disclosure is referring to conventional petroleum derived lubricating base oils produced using 6 petroleum refining processes well documented in the literature and known to 7 those skilled in the art.
9 As used in this disclosure the word "comprises" or "comprising" is intended as an open-ended transition meaning the inclusion of the named elements, but 11 not necessarily excluding other unnamed elements. The phrase "consists 12 essentially of" or "consisting essentially of" is intended to mean the exclusion 13 of other elements of any essential significance to the composition. The phrase 14 "consisting of" or "consists of" are intended as a transition meaning the exclusion of all but the recited elements with the exception of only minor 16 traces of impurities.
18 SUMMARY OF THE INVENTION
The present invention is directed to a process for producing a 21 Fischer-Tropsch derived lubricating base oil blend which comprises blending 22 a Fischer-Tropsch distillate fraction with a Fischer-Tropsch derived bottoms 23 fraction in the proper proportion to produce a Fischer-Tropsch derived 24 lubricating base oil characterized as having a kinematic viscosity of between about 3 and about 10 cSt at 100 degrees C and a TGA Noack volatility of less 26 than about 45 weight percent wherein said distillate fraction is characterized 27 by a kinematic viscosity of about 2 cSt or greater but less than 3 cSt at 28 lo0degreesC.
The Fischer-Tropsch derived bottoms fraction will generally have a kinematic 31 viscosity at 100 degrees C of not less than about 7 cSt. The Fischer- Tropsch 32 derived bottoms fraction may constitute that residual fraction remaining at the 33 bottom of the vacuum column following the fractionation of the waxy material 1 recovered directly from Fischer-Tropsch syncnide, or it may be prepared from 2 the condensate fraction by the oligomerization of the olefins present. Except 3 for bright stock, most Fischer-Tropsch bottoms fractions will have a kinematic 4 viscosity within the range of from about 9 cSt to about 20 cSt at 100 degrees C, preferably, between about 10 cSt and 16 cSt. However, in the 6 case of Fischer-Tropsch derived bright stock the kinematic viscosity may be 7 considerably higher. The invention makes it possible to upgrade the 8 low viscosity Fischer-Tropsch derived base oils into more valuable premium 9 lubricants which otherwise would be cracked or blended into lower value transportation fuels.
12 Bright stock constitutes a bottoms fraction which has been highly refined and 13 dewaxed. Bright stock is a high viscosity base oil. Conventional petroleum 14 derived bright stock is named for the SUS viscosity at 210 degrees F, having viscosities above 180 cSt at 40 degrees C, preferably above 250 cSt at 16 40 degrees C, and more preferably ranging from 500 to 1100 cSt at 17 40 degrees C. Fischer-Tropsch derived bright stock has a kinematic viscosity 18 between about 15 cSt and about 40 cSt at 100 degrees C. Bright stock used 19 to carry out the invention may be produced from Fischer-Tropsch derived residual stocks recovered from the bottom of the vacuum column following the 21 fractionation of the waxy product separated from the syncnide from the 22 Fischer-Tropsch plant. However, Fischer-Tropsch derived bright stock may 23 also be prepared from the oligomerization of the olefins present in the 24 Fischer-Tropsch condensate recovered from the Fischer-Tropsch reactor.
Blending Fischer-Tropsch derived bright stock with the Fischer-Tropsch 26 derived distillate fraction produces a lubricating base oil having especially low 27 volatility, good cold flow properties, and improved oxidation stability as 28 compared to many conventional base oils.
* 30 Lubricating base oils falling within the scope of the invention are blends of at 31 least two different fractions. One fraction is a light distillate fraction and the ,.32 other fraction is a bottoms fraction. Accordingly, lubricating base oils of the 33 invention are distinguished from those homogeneous lubricating base oils I prepared from a single distillate fraction or from only a bottoms fraction.
2 Consequently, the Fischer-Tropsch lubricating base oil blends prepared using 3 the process of the present invention are unique, and will display certain 4 properties which may be used to distinguish the blends from both conventional and from other Fischer-Tropsch derived lubricating base oils 6 disclosed in the prior art. For example, lubricating base oil blends prepared 7 according to the invention will have a TGA Noack volatility of greater than 8 about 12 and more generally will have a TGA Noack volatility in excess of 9 about 20. However, if the blends are intended for use as crankcase lubricating oils they will preferably have a Noack volatility of less than about 11 30 weight percent. The blends also typically will display a VI of between about 12 130 and about 185 and will have very low total sulfur, usually less than about 13 5 ppm. Most noticeably, the lubricating base oils compositions of the invention 14 display unique boiling range distributions.
16 The boiling range distributions characteristic of the lubricating base oils 17 prepared according to the invention will depend to some extent on the 18 properties of the Fischer-Tropsch derived bottoms fraction used in preparing 19 the blend. In general, the lubricating base oils of the invention will have an initial boiling point within the range of between about 550 degrees F 21 (288 degrees C) and about 625 degrees F (330 degrees C) and an end 22 boiling point between about 1000 degrees F (538 degrees C) and about 23 1400 degrees F (760 degrees C). In addition, lubricating base oils of the 24 invention will typically display a bi-modal boiling range distribution which may be described as a lubricating base oil blend in which less than 26 20 weight percent of the blend will boil within the region defined by the 27 50 percent boiling points, plusor minus 30 degrees F. 29 All boiling range distributions in this disclosure are measured using the standard analytical method D-6352 or its equivalent unless stated otherwise.
31 As used herein, a equivalent analytical method to D-6352 refers to any 32 analytical method which gives substantially the same results as the standard 33 method.
1 The Fischer-Tropsch derived lubricating base oil blends prepared according to 2 the present invention also may be blended with conventionally derived 3 lubricating base oils, such as conventional neutral Group I and Group U 4 lubricating base oils. When the Fischer-Tropsch derived lubricating base oil is blended with a conventional neutral Group I or Group II base oil, the 6 conventional base oil will typically comprise between about 40 weight percent 7 and about 90 weight percent of the total blend, with from about 8 40 weight percent to about 70 weight percent being preferred.
The Fischer-Tropsch derived lubricating base oil blends of the invention may 11 also be blended with synthetic lubricants, such as esters (mono-, di-, dimer-, 12 polyol-, and aromatic), potyalphaolefins. Polyphenyl ethers and polygycols.
14 Lubricating base oil blends of the invention represent premium lubricants which may be used to prepare finished lubricants. A finished lubricant, 16 such as, for example, a commercial moW-grade crankcase lubricating oil 17 meeting SAE J300, June 2001 specifications, may be prepared from the 18 lubricating base oil blends of the invention by the addition of the 19 proper additives. Typical additives added to a lubricating base oil blend when preparing a finished lubricant include anti-wear additives, detergents, 21 dispersants, antioxidants, pour point depressants, VI improvers, friction 22 modifiers, demulsifiers, antifoaming agents, corrosion inhibitors, 23 seal swell agents, and the like. In addition, commercial products meeting 24 SAE standards for gear lubricants, NLGI Mark GC and LB for greases, and ISO Viscosity Grade standards for industrial oils may be prepared from the 26 Fischer-Tropsch derived lubricating base oils of the invention.
28 PETAILED DESCRIPTION OF THE INVENTION
Noack volatility of engine oil, as measured by TGA Noack and similar 31 methods, has been found to correlate with oil consumption in passenger car 32 engines. Strict requirements for low volatility are important aspects of several 33 recent engine oil specifications, such as, for example, ACEA A-3 and 6- 3 in 1 Europe and ILSAC GF-3 in North America. Due to the high volatility of 2 conventional low viscosity oils with kinematic viscosities below 3 cSt at 3 100 degrees C, they have limited their use in passenger car engine oils. Any 4 new lubricating base oil stocks developed for use in automotive engine oils should have a volatility no greater than current conventional Group I or 6 Group II light neutral oils.
8 Fischer-Tropsch wax processing typicaliy produces a relatively high 9 proportion of products of low molecular weight and low viscosity that are processed into light products such as naphtha, gasoline, diesel, fuel oil, or 11 kerosene. A proportion of products have kinematic viscosities above 3. 0 cSt 12 which are useful directly as lubricating base oils for many different products, 13 including engine oils. Those base oils with kinematic viscosities between 14 2.1 and 2.8 cSt typically are further processed into lighter products (e.g., gasoline or diesel) in order to be of much economic value. Alternatively, 16 these lOW viscosity Fischer-Tropsch derived base oils may be used in light 17 industrial oils, such as, for example, utility oils, transformer oils, pump oils, or 18 hydraulic oils; many of which have less stringent volatility requirements, and 19 all of which are in much lower demand than engine oils.
21 Lubricating base oils for use in engine oils are in higher demand than those 22 for use in light products. The ability to use a higher proportion of the products 23 from Fischer-Tropsch processes in lubricating base oil blends for engine oils 24 is highly desirable. By virtue of the present invention, Fischer- Tropsch derived lubricating base oils characterized by low viscosity are blended with a 26 Fischer-Tropsch derived bottoms fraction to produce compositions which are 27 useful as a lubricating base oil for preparing engine oil. The lubricating 28 base oil stocks of this invention are comparable in volatility and viscosity to 29 conventional Group I and Group II neutral oils. In addition, lubricating base oils of the invention also have other improved properties, such as very 31 low sulfur and exceptional oxidation stability.
1 Fischer-Tropsch Synthesis 3 During Fischer-Tropsch synthesis liquid and gaseous hydrocarbons are 4 formed by contacting a synthesis gas (syngas) comprising a mixture of hydrogen and carbon monoxide with a Fischer-Tropsch catalyst under 6 suitable temperature and pressure reactive conditions. The Fischer- Tropsch 7 reaction is typically conducted at temperatures of from about 300 degrees to 8 about 700 degrees F (about 150 degrees to about 370 degrees C) preferably 9 from about 400 degrees to about 550 degrees F (about 205 degrees to about 290 degrees C); pressures of from about 10 to about 600 psia, 11 (0.7 to 41 bars) preferably 30 to 300 psia, (2 to 21 bars) and catalyst space 12 velocities of from about 100 to about 10,000 cc/g/hr., preferably 13 300 to 3,000 cc/g/hr.
The products from the Fischer-Tropsch synthesis may range from Ci to 16 C200 plus hydrocarbons with a majority in the C5-C100 pkis range. The reaction 17 can be conducted in a variety of reactor types, such as, for example, 18 fixed bed reactors containing one or more catalyst beds, slurry reactors, 19 fluidized bed reactors, or a combination of different types of reactors. Such reaction processes and reactors are well known and documented in the 21 literature. The slurry Fischer-Tropsch process, which is preferred in the 22 practice of the invention, utilizes superior heat (and mass) transfer 23 characteristics for the strongly exotherrnic synthesis reaction and is able to 24 produce relatively high molecular weight paraffinic hydrocarbons when using.
a cobalt catalyst. In the slurry process, a syngas comprising a mixture of 26 hydrogen and carbon monoxide is bubbled up as a third phase through a 27 sluny which comprises a particulate Fischer-Tropsch type hydrocarbon 28 synthesis catalyst dispersed and suspended in a slurry liquid comprising 29 hydrocarbon products of the synthesis reaction which are liquid under the reaction conditions. The mole ratio of the hydrogen to the carbon monoxide 31 may broadly range from about 0.5 to about 4, but is more typically within the 32 range of from about 0.7 to about 2.75 and preferably from about 0.7 to about 33 2.5. A particularly preferred Fischer-Tropsch process is taught in I European Patent Application No. 0609079, also completely incorporated 2 herein by reference for all purposes.
4 Suitable Fisôher-Tropsch catalysts comprise one or more Group VIII catalytic metals such as Fe, Ni, Co, Ru and Re, with cobalt being preferred.
6 Additionally, a suitable catalyst may contain a promoter. Thus, a preferred 7 Fischer-Tropsch catalyst comprises effective amounts of cobalt and one or 8 more of Re, Ru, Pt, Fe, Ni, Th, Zr, Hf, U, Mg and La on a suitable inorganic 9 support material, preferably one which comprises one or more refractory metal oxides. In general, the amount of cobalt present in the catalyst is 11 between about I and about 50 weight percent of the total catalyst 12 composition. The catalysts can also contain basic oxide promoters such as 13 Th02, La203, MgO, and Ti02, promoters such as Zr02, noble metals (Pt, Pd, 14 Ru, Rh, Os, lr), coinage metals (Cu, Ag, Au), and other transition metals such as Fe, Mn, Ni, and Re. Suitable support materials include alumina, silica, 16 magnesia and titania or mixtures thereof. Preferred supports for cobalt 17 containing catalysts comprise titania. Useful catalysts and their preparation 18 are known and illustrated in U.S. Patent No. 4,568,663, which is intended to 19 be illustrative but non-limiting relative to catalyst selection.
21 The products as they are recovered from the Fischer-Tropsch operation 22 usually may be divided into three fractions, a gaseous fraction consisting of 23 very light products, a condensate fraction generally boiling in the range of 24 naphtha and diesel, and a high boiling Fischer-Tropsch wax fraction which is normally solid at ambient temperatures. The Fischer-Tropsch derived 26 products used to prepare base oils are usually prepared from the waxy 27 fractions of the Fischer-Tropsch syncrude by hydrotreating and/or 28 hydroisomerization. Other methods which may be used in preparing the base 29 oils include oligomerization, solvent dewaxing, atmospheric and vacuum distillation, hydrocracking, hydrofinishing, and other forms of hydroprocessing.
I Hydrojsomei-jzatjon and Solvent Dewaxing 3 Hydroisomerizat ion, or for the purposes of this disclosure simply 4 Isomerization", is intended to improve the cold flow properties of the Fischer-Tropsch derived product by the selective addition of branching into 6 the molecular structure. Isomerization ideally will achieve high conversion 7 levels of the Fischer-Tropsch wax to non-waxy iso-paraflins while at the same 8 time minimizing the conversion by cracking. Since wax conversion can be 9 complete, or at least very high, this process typically does not need to be combined with additional dewaxing processes to produce a lubricating oil 11 base stock with an acceptable pour point. Isomerization operations suitable 12 for use with the present invention typically uses a catalyst comprising an 13 acidic component and may optionally contain an active metal component 14 having hydrogenation activity. The acidic component of the catalysts preferably includes an intermediate pore SAPO, such as SAPO-1 1, SAPO-31, 16 and SAPO-41, with SAPO-1 I being particularly preferred. lntermediate pore 17 zeolites, such as ZSM-22, ZSM-23, SSZ-32, ZSM-35, and ZSM-48, also may 18 be used in can-ying out the isomerization. Typical active metals include 19 molybdenum, nickel, vanadium, cobalt, tungsten, zinc, platinum, and palladium. The metals platinum and palladium are especially preferred as the 21 active metals, with platinum most commonly used.
23 The phrase "intermediate pore size", when used herein, refers to an effective 24 pore aperture in the range of from about 4.0 to about 7.1 Angstrom when the porous inorganic oxide is in the calcined form. Molecular sieves having pore 26 apertures in this range tend to have unique molecular sieving characteristics.
27 Unlike small pore zeolites such as erionite and chabazite, they will allow 28 hydrocarbons having some branching into the molecular sieve void spaces.
29 Unlike larger pore zeolttes such as faujasites and mordenites, they are able to differentiate between n-alkanes and slightly branched alkenes, and larger 31 alkanes having, for example, quatemary carbon atoms. See U.S. Patent 32 No. 5,413,695. The term "SAPO" refers to a silicoaluminophosphate 1 molecular sieve such as described in U.S. Patent Nos. 4,440,871 and 2 5,208,005.
4 In preparing those catalysts containing a non-zeolitic molecular sieve and having an hydrogenation component, it is usually preferred that the metal be 6 deposited on the catalyst using a non-aqueous method. Non-zeolitic 7 molecular sieves include tetrahedrally-coordinated [A102 and P02] oxide units 8 which may optionally include silica. See U.S. Patent No. 5,514,362. Catalysts 9 containing non-zeolitic molecular sieves, particularly catalysts containing SAPO's, on which the metal has been deposited using a non- aqueous method 11 have shown greater selectivity and activity than those catalysts which have 12 used an aqueous method to deposit the active metal. The non-aqueous 13 deposition of active metals on non-zeolitic molecular sieves is taught in 14 U.s. Patent No. 5,939,349. In general, the process involves dissolving a compound of the active metal in a non-aqueous, non-reactive solvent and 16 depositing it on the molecular sieve by ion exchange or impregnation.
18 Solvent dewaxing attempts to remove the waxy molecules from the product by 19 dissolving them in a solvent, such as methyl ethyl ketone, methyl iso- butyl ketone, or toluene, and precipitating the wax molecules and then removing 21 them by filtration as discussed in Chemical Technology of Petroleum, 22 3 Edition, William Gruse and Donald Stevens, 23 McGraw-Hill Book Company, Inc., New York, 1960, pages 566-570. See also 24 U.S. Patent Nos. 4,477,333; 3,773,650; and 3,775,288. In general, with the present invention isomerization is usually preferred over solvent dewaxing, 26 since it results in higher viscosity index products with improved low 27 temperature properties, and in higher yields of the products boiling within the 28 range of the light distillate fraction and the heavy fraction. However solvent 29 dewaxing may be advantageously used in combination with isomerization to recover unconverted wax following isomerization.
1 ijdrotreatinq, Hydrocracking, and Hydrofinishing 3 Hydrotreating refers to a catalytic process, usually carried out in the presence 4 of free hydrogen, in which the primary purpose is the removal of various metal contaminants, such as arsenic; heteroatoms, such as sulfur and nitrogen; or 6 aromatics from the feed stock. Generally, in hydrotreating operations cracking 7 of the hydrocarbon molecules, i.e., breaking the larger hydrocarbon molecules 8 into smaller hydrocarbon molecules, is minimized, and the unsaturated 9 hydrocarbons are either fully or partially hydrogenated.
11 Hydrocracking refers to a catalytic process, usually carried out in the 12 presence of free hydrogen, in which the cracking of the larger hydrocarbon 13 molecules is the primary purpose of the operation. Desulfurization and/or 14 denitrification of the feedstock also usually will occur. Although typically hydrocracking operations will usually be limited to the cracking of the heaviest 16 bottoms material, in the present invention it is one method that may be used 17 to increase amount of olefins present in the Fischer-Tropsch condensate 18 recovered from the Fischer-Tropsch synthesis operation. The olefiri enriched 19 distillate fraction produced from the condensate may be oligomerized to prepare bright stock which is blended with the light fraction to prepare 21 lubricating base oils within the scope of the invention.
23 Catalysts used in carrying out hydrotreating and hydrocracking operations are 24 well known in the art. See for example U.S. Patent Nos. 4,347,121 and 4,810,357, the contents of which are hereby incorporated by reference in their 26 entirety, for general descriptions of hydrotreating, hydrocracking, and of 27 typical catalysts used in each of the processes. Suitable catalysts include 28 noble metals from Group VillA (accordiiig to the 1975 rules of the 29 International Union of Pure and Applied Chemistry), such as platinum or palladium on an alumina or siliceous matrix, and Group VIII and Group VIB, 31 such as nickel-molybdenum or nickel-tin on an alumina or siliceous matrix.
32 U.S. Patent No. 3,852,207 describes a suitable noble metal catalyst and mild 33 conditions. Other suitable catalysts are described, for example, in U. S. Patent I Nos. 4,157,294 and 3,904,513. The non-noble hydrogenation metals, such as 2 nickel-molybdenum, are usually present in the final catalyst composition as 3 oxides, but are usually employed in their reduced or sulfided forms when such 4 sulfide compounds are readily formed from the particular metal involved.
Preferred non-noble metal catalyst compositions contain in excess of about6 5 weight percent, preferably about 5 to about 40 weight percent molybdenum 7 and/or tungsten, and at least about 0.5, and generally about 1 to about 8 15 weight percent of nickel and/or cobalt determined as the corresponding 9 oxides. Catalysts containing noble metals, such as platinum, contain in excess of 0.01 percent metal, preferably between 0.1 and 1.0 percent metal.
11 Combinations of noble metals may also be used, such as mixtures of platinum 12 and palladium.
14 The hydrogenation components can be incorporated into the overall catalyst composition by any one of numerous procedures. The hydrogenation 16 components can be added to matrix component by co-mulling, impregnation, 17 or ion exchange and the Group VI components, i.e.; molybdenum and 18 tungsten can be combined with the refractory oxide by impregnation, 19 co-mulling or co-precipitation.
21 The matrix component can be of many types including some that have acidic 22 catalytic activity. Ones that have activity include amorphous silica- alumina or 23 zeolitic or non-zeolitic crystalline molecular sieves. Examples of suitable 24 matrix molecular sieves include zeolite Y, zeolite X and the so called ultra stable zeolite Y and high structural silica-alumina ratio zeolite Y such as that 26 described in U.S. Patent Nos. 4,401,556; 4,820,402; and 5,059,567. Small 27 crystal size zeolite Y, such as that described in U.S. Patent No. 5, 073,530 can - 28 also be used. Non-zeolitic molecular sieves which can be used include, for 29 example, silicoaluminophosphates (SAPO), ferroaluminophosphate, titanium aluminophosphate and the various ELAPO molecular sieves described in 31 U.S. Patent No. 4,913,799 and the references cited therein. Details regarding 32 the preparation of various non-zeolite molecular sieves can be found in 33 U.S. Patent Nos. 5,114,563 (SAPO) and 4,913,799 and the various 1 references cited in U.S. Patent No. 4,913,799. Mesoporous molecular sieves 2 can also be used, for example the M41 S family of materials as described in 3 J. Am. Chern. Soc., 114:10834-10843(1992)), MCM-41; 4 U.S. Patent Nos. 5,246,689; 5,198,203; and 5,334,368; and MCM-48 (Kresge et al., Nature 359:710 (1992)). Suitable matrix materials 6 may also include synthetic or natural substances as well as inorganic 7 materials such as clay, silica and/or metal oxides such as silicaalumina, 8 silica-magnesia, silica-zirconia, silica-thoria, silica-berylia, silica- titania as well 9 as ternary compositions, such as silica-alumina-thoria, silica-alumina- zirconia, silica-alumina-magnesia, and silica-magnesia zirconia. The latter may be 11 either naturally occurring or in the form of gelatinous precipttates or gels 12 including mixtures of silica and metal oxides. Naturally occurnng clays which 13 can be composited with the catalyst include those of the montmorillonite and 14 kaolin families. These clays can be used in the raw state as originally mined or initially subjected to dealumination, acid treatment or chemical modification.
17 In performing the hydrocracking and/or hydrotreating operation, more than 18 one catalyst type may be used in the reactor. The different catalyst types can 19 be separated into layers or mixed.
21 Hydrocracking conditions have been well documented in the literature. In 22 general, the overall LHSV is about 0.1 hr1 to about 15.0 hr (v/v), preferably 23 from about 0.25 h(1 to about 2.5 hr1. The reaction pressure generally ranges 24 from about 500 psig to about 3500 psig (about 10.4 MPa to about 24.2 MPa, preferably from about 1500 psig to about 5000 psig (about 3.5 MPa to about 26 34.5 MPa). Hydrogen consumption is typically from about 500 to about 27 2500 SCF per barrel of feed (89.1 to 445 m3 H2/m3 feed). Temperatures in the 28 reactor will range from about 400 degrees F to about 950 degrees F (about 29 204 degrees C to about 510 degrees C), preferably ranging from about 650 degrees F to about 850 degrees F (about 343 degrees C to about 31 454 degrees C).
I Typical hydrotreating conditions vary over a wide range. In general, the 2 overall LHSV is about 0.25 to 2.0, preferably about 0.5 to 1.0. The hydrogen 3 partial pressure is greater than 200 psia, preferably ranging from about 4 500 psia to about 2000 psia. Hydrogen recirculation rates are typically greater than 50 SCFIBbI, and are preferably between 1000 and 5000 SCFIBbI.
6 Temperatures in the reactor will range from about 300 degrees F to about 7 750 degrees F (about 150 degrees C to about 400 degrees C), preferably 8 ranging from 450 degrees F to 600 degrees F (230 degrees C to about 9 3l5degreesC).
II Hydrotreating may also be used as a final step in the lube base oil 12 manufacturing process. This final step, commonly called hydrofinishing, is 13 intended to improve the UV stability and appearance of the product by 14 removing traces of aromatics, olefins, color bodies, and solvents. As used in this disclosure, the term UV stability refers to the stability of the lubricating 16 base oil or the fiflShCd lubricant when exposed to UV light and oxygen.
17 Instability is indicated when a visible precipitate forms, usually seen as floc or 18 cloudiness, or a darker color develops upon exposure to ultraviolet light and 19 air. A general description of hydrofinishing may be found in U.S. Patent Nos. 3,852,207 and 4,673,487. Clay treating to remove these impurities is an 21 alternative final process step.
23 Thermal Cracking Thermal cracking may also be employed to crack the paraffin molecules into 26 lower molecular weight olefins in order to olefin enrich the Fischer- Tropsch 27 condensate. As already noted, all Fischer-Tropsch syncrude as initially 28 recovered from the Fisher-Tropsch synthesis will contain olefins. By thermal 29 cracking the paraffin molecules present in the condensate fraction the amount of olefins present may be significantly increased. Following the thermal 31 cracking operation the condensate fraction should have an olefinicity of at 32 least 20 percent by weight, preferably at least 40 percent by weight, and most 33 preferably at least 50 percent by weight.
1 Although batch pyrolysis reactors, such as employed in delayed coking or in 2 cyclic batch operations, could be used to carry out this operation, generally a 3 continuous flow-through operation is preferred in which the feed is first 4 preheated to a temperature sufficient to vaporize most or all of the feed after which the vapor is passed through a tube or tubes. A desirable option is to 6 bleed any remaining nonvaporized hydrocarbons prior to entering the tubes in 7 the cracking furnace. Preferably, the thermal cracking is conducted in the 8 presence of steam which serves as a heat source and also helps suppress 9 coking in the reactor. Details of a typical steam thermal cracking process may be found in U.S. Patent No. 4,042,488, hereby incorporated by reference in its 11 entirety. Although catalyst is generally not used in carrying out the thermal 12 cracking operation, it is possible to conduct the operation in a fluidized bed in 13 which the vaporized feed is contacted with hot fluidized inert particles, such as 14 fluidized particles of coke.
16 In performing the thermal cracking operation, it is preferabie that the feed be 17 maintained in the vapor phase during the cracking operation to maximize the 18 production of olefins. Liquid phase cracking results in the formation of 19 significant amounts of paraffins which are unreactive in the oligomerization operation and, therefore, are not desired. In the pyrolysis zone, the cracking 21 conditions should be sufficient to provide a cracking conversion of greater 22 than about 30 percent by weight of the paraffins present. Preferably, the 23 cracking conversion will be at least 50 percent by weight and most preferably 24 at least 70 percent by weight. The optimal temperature and other conditions in the pyrolysis zone for the cracking operation will vary somewhat depending on 26 the feed. In general, the temperature must be high enough to maintain the 27 feed in the vapor phase but not so high that the feed is overcracked, i.e., the 28 tejnperature and conditions should not be so severe that excessive C4 minus 29 hydrocarbons are generated. The temperature in the pyrolysis zone normally will be maintained at a temperature of between about 950 degrees F 31 (510 degrees C) and about 1600 degrees F (870 degrees C). The optimal 32 temperature range for the pyrolysis zone in order to maximize the production 33 of olefins from the Fischer-.Tropsch wax will depend upon the endpoint of the I feed. In general, the higher the carbon number, the higher the temperature 2 required to achieve maximum conversion. Accordingly, some routine 3 experimentation may be necessary to identify the optimal cracking conditions 4 for a specific feed. The pyrolysis zone usually will employ pressures maintained between about 0 atmospheres and about 5 atmospheres, with 6 pressures in the range of from about 0 to about 2 generally being preferred.
7 Although the optimal residence time of the wax fraction in the reactor will vary 8 depending on the temperature and pressure in the pyrolysis zone, typical 9 residence times are generally in the range of from about 1.5 seconds to about 500 seconds, with the preferred range being between about 5 seconds and 11 about 300 seconds.
13 Oliqomerizat ion Depending upon how the Fischer-Tropsch synthesis is carried out, the 16 Fischer-Tropsch condensate wifl contain varying amounts of OIOfiflS. In 17 addition, most Fischer-Tropsch condensate will contain some alcohols which 18 may be readily converted into olefins by dehydration. As already noted, the 19 condensate may also be olefin enriched through a cracking operation, either by means of hydrocracking or more preferably by thermal cracking. In one 21 embodiment of the present invention these olefins may be oligomerized to 22 produce a Fischer-Tropsch derived bright stock. During oligomerization the 23 lighter olefins are not only converted into heavier molecules, but the carbon 24 backbone of the oligomers will also display branching at the points of molecular addition. Due to the introduction of branching into the molecule, the 26 pour point of the products is reduced.
28 The oligomerization of olefins has been well reported in the literature, and a 29 number of commercial processes are available. See, for example, U.S. Patent Nos. 4,417,088; 4,434,305; 4,827,064; 4,827,073; and 4,990,709. Various 31 types of reactor configurations may be employed, with the fixed catalyst bed 32 reactor being used commercially. More recently, performing the 33 oligomerization in an ionic liquid media has been proposed, since these I catalysts are very active, and the contact between the catalyst and the 2 reactants is efficient and the separation of the catalyst from the 3 oligomerization products is facilitated. The oligomerization reaction will 4 proceed over a wide range of conditions. Typical temperatures for carrying out the reaction are between about 32 degrees F (0 degrees C) and about 6 800 degrees F (425 degrees C). Other conditions include a space velocity 7 from 0.1 to 3 LHSV and a pressure from 0 to 2000 psig. Catalysts for the 8 oligomerization reaction can be virtually any acidic material, such as, for 9 example, zeolites, clays, resins, BF3 complexes, HF, H2S04, Aid3, ionic liquids (preferably ionic liquids containing a Bronsted or Lewis acidic 11 component or a combination of Bronsted and Lewis acid components), 12 transition metal-based catalysts (such as CrISiO2), superacids, and the like. In 13 addition, non-acidic oligomerization catalysts including certain organometallic 14 or transition metal oligomerization catalysts may be used, such as, for example, zirconocenes.
17 Distillation 19 The separation of the Fischer-Tropsch derived products into the various fractions used in the process of the invention is generally conducted by either 21 atmospheric or vacuum distillation or by a combination of atmospheric and 22 vacuum distillation. Atmospheric distillation is typically used to separate the 23 lighter distillate fractions, such as naphtha and middle distiflates, from a 24 bottoms fraction having an initial boiling point above about 700 degrees F to about 750 degrees F (about 370 degrees C to about 400 degrees C). At 26 higher temperatures thermal cracking of the hydrocarbons may take place 27 leading to fouling of the equipment and to lower yields of the heavier cuts.
28 Vacuum distillation is typically used to separate the higher boiling material, 29 such as the lubricating base oil fractions.
31 As used in this disclosure, the term "distillate fraction" or "distillate" refers to a 32 side stream product recovered either from an atmospheric fractionation 33 column or from a vacuum column as opposed to the "bottom fraction" which I represents the residual higher boiling fraction recovered from the bottom of 2 the column. In this disclosure, the term "bottoms" also includes those bottoms 3 fractions and bright stock derived from the oligomerization of olefins present in 4 the Fischer-Tropsch condensate.
6 The Distillate Fraction 8 The distillate fraction used to prepare the lubricating base oil product of the 9 invention represents a distillate fraction of the Fischer-Tropsch derived product as defined above. Distillate fractions used in carrying out the invention 11 and the Fischer-Tropsch derived lubricating base oil blends of the invention 12 may be characterized by their true boiling point (TBP) and by their boiling 13 range distribution. For the purposes of this disclosure, unless stated 14 otherwise, TBP and boiling range distributions for a distillate fraction are measured by gas chromatography according to ASTM D-6352 or its 40.-... .; ,,,I rs it.i 4uivcaiC. IL.
18 A critical property of the distillate fractions of the invention is viscosity. The 19 distillate fraction must have a kinematic viscosity of about 2 or greater but less than 3 cSt at 100 degrees C, more preferably between about 2.1 and 2.8 cSt 21 at 100 degrees C, and most preferably between about 2.2 and 2.7 cSt at 22 l00degreesC.
24 Another critical property of the distillate fractions and the lubricating base oil products of the invention is volatility which is expressed as Noack volatility, 26 Noack volatility is defined as the mass of oil, expressed in weight percent, 27 which is lost when the oil is heated at 250 degrees C and 20 mmHg 28 (2.67 kPa; 26.7 mbar) below atmospheric in a test crucible through which a 29 constant flow of air is drawn for 60 minutes (ASTM 0-5800). A more convenient method for calculating Noack volatility and one which correlates 31 well with ASTM 0-5800 is by using a thermo gravimetric analyzer test (TGA) 32 by ASTM 0-6375. TGA Noack volatility is used throughout this disclosure 33 unless otherwise stated. As already noted above, the first distillate fraction of 1 the invention while having a viscosity below 3 cSt at 100 degrees C displays a 2 significantly lower TGA Noack volatility than would be expected when 3 compared to conventional petroleum-derived distillates having a comparable 4 viscosity. This makes it possible to blend the tow viscosity first distillate fraction with the higher viscosity second distillate fraction and still meet the 6 volatility specifications for the lube base oil and the finished lubricant.
8 The Bottoms Fraction The Fischer-Tropsch derived bottoms fraction represents a high viscosity high 11 boiling fraction. Typically, the bottom fraction will have a kinematic viscosity of 12 at least 9 cSt at 100 degrees C. Fischer-Tropsch derived bottoms other than 13 bright stock will usually have a kinematic viscosity between about 9 cSt and 14 about 20 cSt at 100 degrees C, with a kinematic viscosity of between about 10 cSt and about 16 cSt being preferred. The bottom fraction will contain a 16 large percent of Fischer-Tropsch wax and usually WiH be solid at room 17 temperature. In order to improve its properties prior to being blended with the 18 distillate fraction, it may be advantageous to further process the bottom 19 fraction. For example, the bottom fraction may be hydrotreated to saturate the double bonds and remove any impurities, such as any oxygenates, that may 21 be present The bottoms fraction may also be isomerized to improve its cold 22 flow properties.
24 The Fischer-Tropsch derived bright stock may be prepared by highly refining the waxy bottom fraction recovered directly from a FischerTropsch plant.
26 However, since the Fischer-Tropsch syncrude usually does not comprise a 27 large proportion of heavy products, it may be desirable to prepare at least part 28 of the bright stock through the oligomerization of the otefins present in the 29 Fischer-Tropsch condensate. The enrichment of the Fischer-Tropsch condensate with olefins and the oligomerization of the olefins to produce 31 larger molecules has already been discussed. Typically, the processing of 32 Fischer-Tropsch derived materials to yield bright stock will include dewaxing, 33 hydrofinishing, and fractionation. As already noted, Fischer-Tropsch bright I stock is a high viscosity material having a kinematic viscosity within the range 2 of from about 15 cSt to about 40 cSt at 100 degrees F. 4 Lubricating Base Oil Blends 6 Lubricating base oils are generally materials having a viscosity greater than 7 3 cSt at 100 degrees C; a pour point below 20 degrees C, preferably below 8 0 degrees C; and a VI of greater than 70, preferably greater than 90. As 9 explained below and illustrated in the examples, the lubricating base oil blends prepared according to the process of the present invention meet these 11 criteria. In addition, the lubricating base oils of the invention display a unique 12 combination of properties which could not have been predicted from a review 13 of the prior art relating to both conventional and FischerTropsch materials.
14 The invention takes advantage of the high VI of the light distillate fraction which when blended with the heavier fraction will result in a final blend having 16 a viscosity which is within acceptable limits for use as a lubricating base oiL 18 Lubricating base oils within the scope of the invention will generally have a 19 kinematic viscosity between about 3 and about 10 cSt at 100 degrees C. Generally the lubricating base oil will be blended to a pre-selected target 21 viscosity which is suitable for preparing a finished lubricant intended for a 22 particular application. Obviously the proportions of the various distillate and 23 heavy fractions in the blend will need to be adjusted to meet this desired 24 target viscosity in the lubricating base oil blend. The exact ratio of each of the fractions in the final blend will depend on the exact viscosity of each fraction 26 and the target viscosity desired for the lubricating base oil, as well as other - 27 desired properties such as, for example, VI, volatility, pour point, cloud point 28 and the like.
The lubricating base oil formed by the blending of the distillate fraction and the 31 heavy fraction is characterized as having a viscosity between about 3 and 32 about 10 cSt at 100 degrees C and a TGA Noack volatility of less than about 33 45 weight percent. Generally, the lubricating base oil will have a viscosity I between about 4 cSt and about 8 cSt at 100 degrees C and a Noack volatility 2 greater than about 12 weight percent. Commonly the Noack volatility will be 3 greater than about 20 weight percent. However, if the lubricating base oil 4 blend is intended for use in formulating a crankcase lubricating oil, the Noack volatility preferably will be less than about 30 weight percent. Volatility of the 6 Fischer-Tropsch derived lubricating base oil blends of the invention are 7 acceptable and are comparable to conventional petroleum derived lubricating 8 base oils which is surprising given the low viscosity of the distillate fraction.
9 The use of a comparable petroleum derived base oil in a lubricating base oil blend would result in an unacceptably high Noack volatility. Generally, the 11 viscosity index (VI) of the Fischer-Tropsch derived lubricating base oil blend 12 will be between about 130 and about 185. VI is an expression of the effect of 13 temperature on viscosity, and it is surprising that a lubricating base oil blend 14 prepared using a base oil having a viscosity of less than 3 cSt at 100 degrees C will be characterized by such a favorable VI. As noted 16 previously, it is even more surprising that the blends of the invention often 17 realize a VI premium, i.e., the VI of the lubricating base oil blend is higher than 18 would be expected from an averaging of VI of the light distillate fraction with 19 that of the heavy fraction. Since Fischer-Tropsch derived hydrocarbons are typically very low in total sulfur, the total sulfur content of the lubricating base 21 oil usually will be less than about 5 ppm. Conventionally- derived, solvent 22 processed lubricating base oils will generally display much higher sulfur 23 levels, usually in excess of 2000 ppm.
Lubricating base oil blends within the scope of the invention will generally 26 have a boiling range distribution of at least 450 degrees F (about 27 232 degrees C). Typically, the Fischer-Tropsch derived!ubricating base oil 28 blend will have an initial boiling point within the range of between about 29 550 degrees F (288 degrees C) and about 625 degrees F (330 degrees C), an end boiling point between about 1000 degrees F (538 degrees C) and about 31 1400 degrees F (760 degrees C), and wherein less than 20 weight percent of 32 the blend boils within the region defined by the 50 percent boiling point, plus 33 or minus 30 degrees F (16.7 degrees C). The boiling range distribution of the I lubricating base oils of the invention are significantly broader than those 2 observed for conventional lubricating base oils. The boiling range for 3 conventionally derived lubricating base oils typically will not exceed about 4 250 degrees F (about 139 degrees C). In this disclosure when referring to boiling range distribution, the boiling range between the 5 percent and 6 95 percent boiling points is what is referred to.
8 Pour point is the temperature at which a sample of the lubricating base oil will 9 begin to flow under carefully controlled conditions. In this disclosure, where pour point is given, unless stated otherwise, it has been determined by 11 standard analyticJ method ASTM D-5950. Lubricating base oils prepared 12 according to the present invention have excellent pour points which are 13 comparable or even below the pour points observed for conventionally 14 derived lubricating base oils. In addition, the blends containing the distillate fraction and bright stock have been observed to display a cloud point 16 premium, i.e., the cloud point is significantly lower than would have been 17 predicted from the mere averaging of the cloud points of the two components 18 making up the blend. In some cases the cloud point will actually be 19 significantly lower than the cloud point of either component. Preferably the cloud point of such blends will be -15 degrees C or less. Finally, due to the 21 extremely low aromatics and multi-ring naphthene levels of blends of 22 Fischer-Tropsch derived lubricating base oils; their oxidation stability far 23 exceeds that of conventional lubricating base oil blends.
A useful property of lubricating base oils and finished lubricants intended for 26 use in automobile engine oils is measured by cold-cranking simulator (CCS) 27 apparent viscosity which correlates with low temperature cranking. It is 28 measured by ASTM D5293 at a set temperature between -10 and - 29 35 degrees C. Engine oil specifications, e.g., SAE J300, include maximum limits for CCS Viscosity for multi-grade engine oils. For a finished lubricant 31 within the scope of the invention the cold-cranking simulator (CCS) apparent 32 viscosity should be less than 7000 cP at -25 degrees C and preferably of 1 6500 cP or less at -25 degrees C if the lubricant is intended for use as a 2 multi-grade engine oil in an automobile engine.
4 Finished Lubricants 6 Finished lubricants generally comprise a lubricating base oil and at least 7 one additive. Finished lubricants are used in automobiles, diesel engines, gas 8 engines, axles, transmissions, and industrial applications. As noted above, 9 finished lubricants must meet the specifications for their intended application as defined by the concerned governing organization. Lubricating base oils of 11 the present invention have been found to be suitable for formulating finished 12 lubricants intended for many of these applications. For example, lubricating 13 base oils of the present invention may be utilized in formulations to meet 14 SAE J300, June 2001 specifications for I OW-X)(, and I 5W-XX multi- grade crankcase lubricating oils. Although some multi-grade crankcase oils meeting 16 may be formulated using only Fischer-Tropsch lubricating base oils prepared 17 according to the present invention, in order to meet the specifications for 18 some 1 OW-XX and most 1 5W-XX, it may be desirable that the 19 Fischer-Tropsch derived lubricating base oil be blended with a conventional petroleum derived lubricating base oil, such as a conventional neutral Group I 21 or Group II base oil to meet the specifications. Typically, when present the 22 conventionaj neutral Group I or Group II base oil will comprise from about 23 40 to about 90 weight percent of the lubricating base oil blend, more 24 preferably from about 40 to about 70 weight percent. Also FischerTropsch derived lubricating oils of the invention may be used to formulate mono-grade 26 engine oils, such as SAE 20 or SAE 30, which are heavily used in many parts - 27 of the world where low temperature performance is not critical. In addition, 28 Fischer-Tropsch derived lubricating base oils of the invention may be used to 29 formulate finished lubricants meeting the specifications for automatic transmission fluids, NLGI Mark GC and LB greases, and ISO Viscosity 31 Grade 22, 32, and 46 industrial oils.
I The lubricating base oil compositions of the invention may also be used as a 2 blending component with other oils. For example, the Fischer-Tropsch derived 3 lubricating base oils may be used as a blending component with synthetic 4 base oils, such as esters (mono-, di-, dimer, polyol-, and aromatic), polyalphaolefins, polyphenyl ethers, and polyglycols to improve the viscosity 6 and viscosity index properties of those oils. The Fischer-Tropsch derived base 7 oils may be combined with isomerized petroleum wax. They may also be used 8 as workover fluids, packer fluids, coring fluids, completion fluids, and in other 9 oil field and well-servicing applications. For example, they can be used as spotting fluids to release a drill pipe which has become stuck, or they can be II used to replace part or all of the expensive polyalphaolefin lubricating 12 additives in downhole applications. Additionally, Fischer-Tropsch derived 13 lubricating base oils may be used in drilling fluid formulations where 14 shale-swelling inhibition is important, such as described in U.S. Patent No.4,941,981.
17 Additives which may be blended with the lubricating base oil to form the 18 finished lubricant composition include those which are intended to improve 19 certain properties of the finished lubricant. Typical additives include, for example, anti-wear additives, detergents, dispersants, antioxidants, pour point 21 depressants, VI improvers, friction modilfiers, demulsifiers, antifoaming 22 agents, corrosion inhibitors; seal swell agents, and the like. Other 23 hydrocarbons, such as those described in U.S. Patent Nos. 5,096,883 and 24 5,189,012, may be blended with the lubricating base oil provided that the finished lubricant has the necessary pour point, kinematic viscosity, flash 26 point, and toxicity properties. Typically, the total amount of additives in the 27 finished lubricant will fall within the range of from about I to about 28 30 weight percent. However due to the excellent properties of the 29 Fischer-Tropsch derived lubricating base oils of the invention, less additives than required with conventional petroleum derived base oils may be required 31to meet the specifications for the finished lubricant. The use of additives in 32 formulating finished lubricants is well documented in the literature and well I within the ability of one skilled in the art. Therefore, additional explanation
2 should not be necessary in this disclosure.
4 EXAMPLES
6 The following examples are included to further clarify the invention but are not 7 to be construed as limitations on the scope of the invention.
9 Example I
11 Two Fisher-Tropsch distillate fractions (designated FT-2.2 and FT-2.4, 12 respectively) having kinematic viscosities between 2 and 3 cSt at 13 100 degrees C were recovered from a Fischer-Tropsch syncrude prepared 14 using a cobalt-based catalyst. Each fraction was analyzed and their properties were compared to two commercially available conventional petroleum derived 16 oils (Nexbse 3020 and Pennzoil 75HC) having viscosities within the same 17 general range. A comparison between the properties of the four samples is 18 shown below: FT-2.2 FT-2.4 Nexbase 3020 Pennzoll 75HC 22 Vis. @ 1000 C (cst) 2.18 2.399 2.055 2.885 23 Viscosity Index (VI) 123 125 96 80 24 Pour Pohit, C -37 -33 -51 -38 Noack (WI %) 52.3 56.64 75.1 59.1 27 It should be noted that, although the viscosity at 100 degrees C of the 28 two Fischer-Tropsch derived materials were comparable to those of the 29 conventional oils, the VI is surprisingly high, which results in a much lower volatility for a given viscosity. -
32 Example 2
34 A Fisher-Tropsch bottom fraction, designated FT-14, was recovered from a Fischer-Tropsch syncrude prepared using an iron-based catalyst. The bottom I fraction was subsequently hydrotreated. The properties of FT-14 were as 2 follows: p 4 Viscosity at 100 degrees C (cSt) 14.62 Viscosity Index (VI) 160 6 Pour Point, C -1
8 Example 3
Two different Fischer-Tropsch derived lubricating base oil blends were 11 prepared by blending different proportions of the FT-2.4 from example 1 and 12 FT-14 from example 2. The proportions of FT-2.4 and FT-14 in each blend are 13 shown in Table I below:
Table I
I Wt % FT-2.2 Wt % FT-14 Lubricating Base Oil A 60 40 I Lubricating Base Oil B 35 65 17 The properties for each of the lubricating base oil blends are summarized in
18 Table 2 below:
______________________ Table 2 _______________ ________________________ Lubricating Base Oil A Lubricating Base Oil B 0-2887 Simulated TBP (WT%), F _______________ _______________ TSP @0.5 (Initial Boiling Point) 593 596 TBP@5 616 634 TBP@10 630 659 TSP @20 656 708 TSP @30 680 765 TSP @40 705 1015 TSP @50 730 1032 TSP @60 760 1049 TBP@70 996 1065 TSP @80 1027 1089 TSP @90 1057 1136 TSP @95 1079 1182 TSP @995 1132 1251 Boiling Range Distribution (5-95) 463 548 Viscosity at 40 c 21.00 38.62 Viscosity at 100 C 4.969 7.718 Viscosity Index 174 i74 Pour Point, c -29 _______________ CCS at -25 C. cP ________________ 293 CCS at -35 C, cP 1058 8570 TGA Noack 37.55 2247 21 This property represents cold-cranking simulator (CCS) apparent viscosity which Is a measure of low 22 temperature cold-cranking in automobile engines determined by ASTM 05293.
1 It should be noted that both Fischer-Tropsch blends had volatilities, as 2 measured by TGA Noack, which was suitable for blending engine oils. It 3 should also be noted that the VI of each of the blends was higher than the VI 4 of either FT-2.4 or FT-14 indicating that the blends were realizing a VI premium.
7 Example 4
9 The properties of the Fischer-Tropsch derived lubricating base oils as shown in Table 2 above may be compared to the properties of commercially 11 available petroleum derived conventional Group I and Group II light neutral 12 base oils as summarized in Table 3 below.
14 ________________ ___________ TabIe3 _________ ___________ ChevronTexaco Generic Gulf Coast Gulf Coast Exxon Americas I ______________________ IOOR Solvent 100 H.P. 100 Core 100 [API Base Oil Category II I II ________________ IJPI 1509 E1.3) _____________ _______________ __________ _____________ D-6352 Simulated TBP TBP@5 659 _____________ _________ 647 TSP @10 - 677 ______________ __________ 672 TSP @20 703 _______________ __________ 703 TSP @30 723 _______________ __________ 725 TBP@50 756 ____________ _________ 761 TSP @70 786 ________________ ___________ 796 TBP @90 825 _______________ __________ 839 TBP @95 842 _______________ __________ 858 TBP @99.5 878 ________________ ___________ 907 Bofling Range DIstribution 219 211 (5-95) __________ ___________ ________ __________ Viscosity at 40 C 20.0 20.4 20.7 20.2 Viscosity at 100 C 4.1 4.1 4.1 4.04 Viscosity Index 102 97 97 - 95 Pour Point, C -14 -18 -15 -19 CCSaL-25 C,cP 1450 14,30 1550 1513 CCS at -35 C, cP >3000 >3000 >3000 >3000 Noack Volatility, wt% 26 29 25.5 29.3 16 A comparison of Table 2 and 3 illustrate that the Fischer-Tropsch derived 17 lubricating base oils have a similanNoack volatility to conventional Group I 18 and Group II light neutral oils. The kinematic viscosity of 19 Lubricating Base Oil A was comparable to that of the Group I and Group II light neutral oils while that of Lubricating Base Oil B was significantly higher.
21 Lubricating Base Oil A displays a lower pour point than the conventional light 1 neutral oils. The Fischer-Tropsch derived lubricating base oils of the invention 2 also display significantly better VI values.
I
4 Example 5
6 A lubricating base oil blend was prepared which contained 25 weight percent 7 of FT-2.2 and 75 weight percent of FT-14. The kinematic viscosity at 8 100 degrees C was found to be 9.007 and the VI was 173. Once again the 9 blend displays a VI premium over the Vi's of both FT-2.2 and FT-14.
11 Example 6
13 A Fisher-Tropsch distillate fraction designated FT-2.5 was blended with a 14 Fischer-Tropsch derived bright stock designated FT-BS that was prepared by oligomerizing the olefins in a Fischer-Tropsch derived feed. The properties of 16 the two Fischer-Tropsch derived feeds were as follows: 18 FT-2.5 FT-BS Vis. 1000 C (cSt) 2.583 30.12 21 Viscosity index (VI) 133 132 22 Pour Point, C -30 -46 23 Cloud Point, C -16 -10 24 Noack (wt. %) 48.94 26 Two different Fischer-Tropsch derived lubricating base oil blends were 27 prepared and the respective proportions of FT-2.5 and FT-BS in each blend 28 are shown in Table 4 below:
Table 4
- Wt % FT-2.5 Wt % FT-BS Lubricating Base Oil C 70 30 Lubricating Base Oil D 30 70 1 The properties for each of the lubricating base oil blends are summarized in
2 Table 5 below:
4 __________________ Table5 ____________ __________________________ Lubnrating Base Oil C UJbritingse Oil 0 D-2887 Simulated TBJWT%), F _________________ _________________ TBP @0.5 (Initial Boiling Point) 599 604 TSP@5 617 634 TBP10 630 664 TBP@20 656 728 TSP @30 684 809 TBP@40 711 1048 TSP @50 739 1114 TBP@6C) 773 1165 TSP t70 809 1210 TSP @80 1111 1261 TSP @90 1226 1312 TSP @5 1288 1335 TSP @99. 5 1349 1373 Boiling Range Dislribution (5-95) 671 701 Viscosity at 40 C 20.70 84.14 Viscosity at 100 C 4.799 12.58 Viscosity Index 162 147 Pour Point, C -23 -33 Cloud Point, C -16 -23 CCS at -20 C. cP _________________ 4,017 CS at -25 C, cP __________________ 6,665 cSat- 3cfC.cP. 1,186 11,911 L!GANOaCk I 34.55 14.52 This property represents cold-cranking simulator (CCS) apparent viscosity whith is a measure of low 6 temperature cold-cranking in automobile engines determined by ASTM D- 5293.
8 It should be noted that both Fischer-Tropsch blends had excellent VI, 9 low pour points, and low cloud points. Note particularly the VI of the blends which demonstrate a VI premium when compared to the Vi's for FT-2. 5 and 11 FT-BS. Also note the significant improvement in cloud point as compared with 12 FT-BS. Note that the cloud point for lubricating base oil D displays a cloud 13 point premium, i.e., the cloud point is significantly lower than that for either 14 FT-2.5 or FT-BS. Base oils with a premium cloud point have utility in products which require cold filtration, such as, for example, refrigeration oils.
16 Base oil C, although too high in volatility to be used in engine oils alone, can 17 be further blended as a minority component for engine oils, or used as a 18 majority component in many other lubricant applications, such as, for 19 example, transmission fluids, industrial oils, diluent oils, spray oils, process oils, hydraulic oils, and the like. Base oil D can be used to make 21 15W 40 engine oil with no added viscosity modifier.
Claims (24)
- Claims: 1. A process for producing a Fischer-Tropsch derived lubricatingbase oil blend which comprises blending a Fischer-Tropsch distillate fraction with a Fischer-Tropsch derived bottoms fraction in suitable proportions to produce a Fischer-Tropsch derived lubricating base oil characterized as having a kinematic viscosity of between 3 and 10 cSt at 100 C and a TGA Noack volatility of less than 45 weight percent wherein said distillate fraction is characterised by a kinematic viscosity of 2 cSt or greater but less than 3 cSt at 100 C, and wherein the Fischer-Tropsch distillate fraction is the only distillate fraction blended into the Fischer-Tropsch derived lubricating base oil blend.
- 2. The process of claim 1 wherein the distillate fraction has a viscosity between 2.1 and 2.8 cSt at 100 C.
- 3. The process of claim 2 wherein the distillate fraction has a viscosity between 2.2 and 2.7 cSt at 100 C.
- 4. The process of claim 1 wherein the Fischer-Tropsch derived bottoms fraction has a kinematic viscosity between 9 cSt and 20 cSt at 100 C.
- 5. The process of claim 4 wherein the bottoms fraction has a viscosity of between 10 and 16 cSt at 100 C.
- 6. The process of claim I wherein the Fischer-Tropsch derived bottoms fraction is bright stock.
- 7. The process of claim 6 wherein the bright stock is produced by oligomerizing the olefins present in an olefin-containing Fischer-Tropsch derived condensate. -32 -
- 8. The process of claim 7 including the preliminary step of enriching the olefins in the Fischer-Tropsch condensate by the dehydration of the alcohols present in the condensate.
- 9. The process of claim 7 including the preliminary step of enriching the olefins in the Fischer-Tropsch condensate by the thermal cracking of the hydrocarbons present in the condensate.
- 10. The process of claim I wherein the lubricating base oil blend has a Noack volatility of less than 30 weight percent.
- 11. The process of claim 1 including the additional step of blending the Fischer-Tropsch lubricating base oil blend with at least one additive to produce a finished lubricant.
- 12. A Fischer-Tropsch derived lubricating base oil blend produced by a process according to any one of claims 1 to 10.
- 13. The Fischer-Tropsch derived lubricating base oil blend according to claim 12, characterized by a viscosity of between 3 and 10 cSt at 100 C; a TGA Noack volatility of less than 45 weight percent; an initial boiling point within the range of between 550 F (288 C) and 625 F (329 C); an end boiling point between 1000 degrees F (538 C) and 1400 F (760 C); and wherein less than 30 weight percent of the blend boils within the region defined by the 50 percent boiling points, plus or minus 25 F (14 C).
- 14. The Fischer-Tropsch derived lubricating base oil blend of claim 13 having a boiling range distribution of at least 450 F (250 C) between the 5 percent and 95 percent points as measured by analytical method D-6352 or its equivalent. -33 -
- 15. The Fischer-Tropsch lubricating base oil blend of claim 13 wherein the TGA Noack volatility is 12 weight percent or greater.
- 16. The Fischer-Tropsch lubricating base oil blend of claim 15 wherein the TGA volatility is greater than 20 weight percent.
- 17. The Fischer-Tropsch lubricating base oil blend of claim 13 wherein the TGA volatility is less than 30 weight percent.
- 18. The Fischer-Tropsch lubricating base oil blend of claim 13 wherein the VI is between 130 and 185.
- 19. The Fischer-Tropsch lubricating base oil blend of claim 13 wherein the total sulfur content is less than 5 ppm.
- 20. A finished lubricant comprising a Fischer-Tropsch derived lubricating base oil blend according to claims 12 -19 and at least one additive.
- 21. The finished lubricant of claim 20 which is suitable for use as an engine oil crankcase lubricant.
- 22. A process for producing a Fischer-Tropsch derived lubricating base oil blend, substantially as hereinbefore described, with reference to the accompanying examples.
- 23. A Fischer-Tropsch derived lubricating base oil blend, substantially as hereinbefore described, with reference to the accompanying examples.
- 24. A finished lubricant comprising a Fischer-Tropsch derived lubricating base oil blend, substantially as hereinbefore described, with reference to the accompanying examples.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/387,211 US7141157B2 (en) | 2003-03-11 | 2003-03-11 | Blending of low viscosity Fischer-Tropsch base oils and Fischer-Tropsch derived bottoms or bright stock |
| GB0518972A GB2417037B (en) | 2003-03-11 | 2004-02-19 | Blending of low viscosity Fischer-Tropsch base oils and Fischer-Tropsch derived bottoms or bright stock |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB0625619D0 GB0625619D0 (en) | 2007-01-31 |
| GB2430681A true GB2430681A (en) | 2007-04-04 |
| GB2430681B GB2430681B (en) | 2007-10-24 |
Family
ID=38530003
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB0625619A Expired - Fee Related GB2430681B (en) | 2003-03-11 | 2004-02-19 | Blending of low viscosity Fischer-Tropsch base oils and Fischer-Tropsch derived bottoms or bright stock |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2430681B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2461654A (en) * | 2005-06-22 | 2010-01-13 | Chevron Usa Inc | Lower ash lubricating oil with low cold cranking simulator viscosity |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2392673A (en) * | 2002-09-04 | 2004-03-10 | Chevron Usa Inc | Fischer-Tropsch lubricants having specified viscosity |
-
2004
- 2004-02-19 GB GB0625619A patent/GB2430681B/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2392673A (en) * | 2002-09-04 | 2004-03-10 | Chevron Usa Inc | Fischer-Tropsch lubricants having specified viscosity |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2461654A (en) * | 2005-06-22 | 2010-01-13 | Chevron Usa Inc | Lower ash lubricating oil with low cold cranking simulator viscosity |
| GB2461654B (en) * | 2005-06-22 | 2010-03-03 | Chevron Usa Inc | Lower ash lubricating oil with low cold cranking simulator viscosity |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2430681B (en) | 2007-10-24 |
| GB0625619D0 (en) | 2007-01-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7141157B2 (en) | Blending of low viscosity Fischer-Tropsch base oils and Fischer-Tropsch derived bottoms or bright stock | |
| US6703353B1 (en) | Blending of low viscosity Fischer-Tropsch base oils to produce high quality lubricating base oils | |
| AU2003257900B2 (en) | Blending of low viscosity Fischer-Tropsch base oils with conventional base oils to produce high quality lubricating base oils | |
| US6773578B1 (en) | Process for preparing lubes with high viscosity index values | |
| JP5033280B2 (en) | High-grade synthetic lubricant base oil | |
| AU2002301444B2 (en) | Lube base oils with improved yield | |
| US6332974B1 (en) | Wide-cut synthetic isoparaffinic lubricating oils | |
| NZ527907A (en) | Process to prepare a lubricating base oil and a gas oil from Fischer-Thopsch product | |
| GB2384247A (en) | Distillate fuel blends with improved seal swell properties | |
| US20090159492A1 (en) | Process to prepare a lubricating base oil and its use | |
| GB2430681A (en) | Fischer-Tropsch lubricant base oil | |
| GB2386608A (en) | Preparation of lube base stocks having specific pour-cloud spread value |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20130219 |