US20040172876A1 - Catalytic metal additive concentrate and method of making and using - Google Patents
Catalytic metal additive concentrate and method of making and using Download PDFInfo
- Publication number
- US20040172876A1 US20040172876A1 US10/394,693 US39469303A US2004172876A1 US 20040172876 A1 US20040172876 A1 US 20040172876A1 US 39469303 A US39469303 A US 39469303A US 2004172876 A1 US2004172876 A1 US 2004172876A1
- Authority
- US
- United States
- Prior art keywords
- fuel
- cerium
- platinum
- polymer
- catalytic metal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000654 additive Substances 0.000 title claims abstract description 63
- 230000000996 additive effect Effects 0.000 title claims abstract description 50
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 49
- 239000002184 metal Substances 0.000 title claims abstract description 49
- 239000012141 concentrate Substances 0.000 title claims abstract description 26
- 230000003197 catalytic effect Effects 0.000 title claims abstract description 23
- 238000004519 manufacturing process Methods 0.000 title description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract description 122
- 239000000446 fuel Substances 0.000 claims abstract description 109
- 229920000642 polymer Polymers 0.000 claims abstract description 76
- 229910052684 Cerium Inorganic materials 0.000 claims abstract description 73
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims abstract description 73
- 239000000203 mixture Substances 0.000 claims abstract description 55
- 229910052697 platinum Inorganic materials 0.000 claims abstract description 55
- 239000007787 solid Substances 0.000 claims abstract description 46
- 239000003054 catalyst Substances 0.000 claims abstract description 42
- 239000002816 fuel additive Substances 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims abstract description 32
- 238000002485 combustion reaction Methods 0.000 claims abstract description 18
- 239000002904 solvent Substances 0.000 claims description 32
- 238000009835 boiling Methods 0.000 claims description 18
- 239000006185 dispersion Substances 0.000 claims description 16
- 239000000344 soap Substances 0.000 claims description 14
- KLFRPGNCEJNEKU-FDGPNNRMSA-L (z)-4-oxopent-2-en-2-olate;platinum(2+) Chemical compound [Pt+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O KLFRPGNCEJNEKU-FDGPNNRMSA-L 0.000 claims description 8
- 239000004305 biphenyl Substances 0.000 claims description 8
- 238000002156 mixing Methods 0.000 claims description 8
- 238000001704 evaporation Methods 0.000 claims description 3
- 238000001802 infusion Methods 0.000 claims 6
- 239000000463 material Substances 0.000 abstract description 17
- 238000013459 approach Methods 0.000 abstract description 5
- 239000002283 diesel fuel Substances 0.000 abstract description 5
- 239000002131 composite material Substances 0.000 abstract description 4
- 238000005538 encapsulation Methods 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 3
- VIEYMVWPECAOCY-UHFFFAOYSA-N 7-amino-4-(chloromethyl)chromen-2-one Chemical compound ClCC1=CC(=O)OC2=CC(N)=CC=C21 VIEYMVWPECAOCY-UHFFFAOYSA-N 0.000 description 53
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 33
- 239000003921 oil Substances 0.000 description 19
- 235000019198 oils Nutrition 0.000 description 18
- 229910052742 iron Inorganic materials 0.000 description 17
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- -1 demulsifiers Substances 0.000 description 14
- 150000003058 platinum compounds Chemical class 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 230000008569 process Effects 0.000 description 10
- 238000012545 processing Methods 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 9
- 238000004090 dissolution Methods 0.000 description 8
- 229930195733 hydrocarbon Natural products 0.000 description 8
- 150000002430 hydrocarbons Chemical class 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 238000009792 diffusion process Methods 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 229940097789 heavy mineral oil Drugs 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 6
- 230000007246 mechanism Effects 0.000 description 6
- 238000004821 distillation Methods 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
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- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 229940049964 oleate Drugs 0.000 description 4
- 238000005292 vacuum distillation Methods 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 3
- 239000002828 fuel tank Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 230000003641 microbiacidal effect Effects 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 239000008149 soap solution Substances 0.000 description 3
- 238000000935 solvent evaporation Methods 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 150000001785 cerium compounds Chemical class 0.000 description 2
- FXNONNRUNQPNLF-UHFFFAOYSA-N cerium;2-ethylhexanoic acid Chemical compound [Ce].CCCCC(CC)C(O)=O.CCCCC(CC)C(O)=O.CCCCC(CC)C(O)=O FXNONNRUNQPNLF-UHFFFAOYSA-N 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000010763 heavy fuel oil Substances 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 125000005474 octanoate group Chemical group 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 239000012056 semi-solid material Substances 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- 239000004071 soot Substances 0.000 description 2
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
- QLZJUIZVJLSNDD-UHFFFAOYSA-N 2-(2-methylidenebutanoyloxy)ethyl 2-methylidenebutanoate Chemical compound CCC(=C)C(=O)OCCOC(=O)C(=C)CC QLZJUIZVJLSNDD-UHFFFAOYSA-N 0.000 description 1
- YPIFGDQKSSMYHQ-UHFFFAOYSA-M 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC([O-])=O YPIFGDQKSSMYHQ-UHFFFAOYSA-M 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229910017147 Fe(CO)5 Inorganic materials 0.000 description 1
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical class [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 1
- 239000004165 Methyl ester of fatty acids Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 125000005595 acetylacetonate group Chemical group 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000000828 canola oil Substances 0.000 description 1
- 235000019519 canola oil Nutrition 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- HZMBANJECWHRGE-GNOQXXQHSA-K cerium(3+);(z)-octadec-9-enoate Chemical compound [Ce+3].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O HZMBANJECWHRGE-GNOQXXQHSA-K 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 1
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 150000002506 iron compounds Chemical class 0.000 description 1
- HOIQWTMREPWSJY-GNOQXXQHSA-K iron(3+);(z)-octadec-9-enoate Chemical compound [Fe+3].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O HOIQWTMREPWSJY-GNOQXXQHSA-K 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/06—Use of additives to fuels or fires for particular purposes for facilitating soot removal
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/143—Organic compounds mixtures of organic macromolecular compounds with organic non-macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/1814—Chelates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1881—Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
- C10L1/301—Organic compounds compounds not mentioned before (complexes) derived from metals
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
- C10L1/305—Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond)
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/02—Use of additives to fuels or fires for particular purposes for reducing smoke development
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B51/00—Other methods of operating engines involving pretreating of, or adding substances to, combustion air, fuel, or fuel-air mixture of the engines
- F02B51/02—Other methods of operating engines involving pretreating of, or adding substances to, combustion air, fuel, or fuel-air mixture of the engines involving catalysts
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02M—SUPPLYING COMBUSTION ENGINES IN GENERAL WITH COMBUSTIBLE MIXTURES OR CONSTITUENTS THEREOF
- F02M27/00—Apparatus for treating combustion-air, fuel, or fuel-air mixture, by catalysts, electric means, magnetism, rays, sound waves, or the like
- F02M27/02—Apparatus for treating combustion-air, fuel, or fuel-air mixture, by catalysts, electric means, magnetism, rays, sound waves, or the like by catalysts
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23C—METHODS OR APPARATUS FOR COMBUSTION USING FLUID FUEL OR SOLID FUEL SUSPENDED IN A CARRIER GAS OR AIR
- F23C13/00—Apparatus in which combustion takes place in the presence of catalytic material
- F23C13/08—Apparatus in which combustion takes place in the presence of catalytic material characterised by the catalytic material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/16—Hydrocarbons
- C10L1/1616—Hydrocarbons fractions, e.g. lubricants, solvents, naphta, bitumen, tars, terpentine
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/16—Hydrocarbons
- C10L1/1625—Hydrocarbons macromolecular compounds
- C10L1/1633—Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds
- C10L1/1641—Hydrocarbons macromolecular compounds homo- or copolymers obtained by reactions only involving carbon-to carbon unsaturated bonds from compounds containing aliphatic monomers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1886—Carboxylic acids; metal salts thereof naphthenic acid
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/188—Carboxylic acids; metal salts thereof
- C10L1/1888—Carboxylic acids; metal salts thereof tall oil
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- 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
- Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
- Y02T10/00—Road transport of goods or passengers
- Y02T10/10—Internal combustion engine [ICE] based vehicles
- Y02T10/12—Improving ICE efficiencies
Definitions
- the invention concerns a new process for improving the delivery of metallic combustion catalysts to internal combustion engines and other combustion devices and to enable the production of additive delivery means which have the ability to effect the slow and positive supply of metallic additives, including platinum containing catalyst compositions, to fuel.
- the also invention provides additive release materials and methods designed for compatibility with various on-board delivery mechanisms.
- Davis discloses a dissolvable element in U.S. Pat. No. 5,507,942.
- He provides a fuel filter assembly including a fuel additive element formed into a hollow cylindrical dissolvable insert comprising fuel additive in a wax substrate.
- the fuel additive comprises a microbiocide that is compatible with combustion systems and fuels and which is more soluble in fuel than water.
- the microbiocide is encapsulated in the wax substrate, which has a high melting point and a burning characteristic for proper release of the microbiocide without compromising exhaust gas emissions and without unduly releasing an excessive amount of fuel additive that may adversely affect engine and fuel components.
- the fuel additive may also comprise cetane improvers, antioxidants, stabilizers, combustion improvers and emission reducers.
- the wax substrate is fabricated from a paraffin, which is said to be a hydrocarbon mixture with clean burning characteristics.
- the insert is housed within the hollow cylinder of a fuel filter canister. It is supported in a vertical orientation and slowly releases the fuel additive upon dissolving the wax substrate.
- a fuel filter including a fuel additive that can be released into fuel.
- the rate of release for the fuel is said to be controlled to a substantially constant rate to maintain a uniform level of fuel additive in the fuel.
- Fuel from a filter chamber migrates through a diffusion orifice into an inner chamber and contacts an additive tablet which can have an outer coating. Fuel diffuses through the coating to contact a fuel additive composition, which dissolves in the fuel to provide a fuel composition comprising the dissolved additive. The fuel composition diffuses back through the coating into the inner chamber where it mixes with fuel.
- the fuel additives can be liquid or solid, and two or more fuel additives can be combined and can be compounded with a suitable polymer. They can be either a solid or semisolid material in a form, such as tablet, to control the rate of release of the additive into the fuel.
- the fuel additive can further include a wide variety of binders, compounding agents and mold release agents. When the additive is provided in liquid form, it is preferably combined with a suitable agent to form a solid or semisolid material.
- the term fuel additive includes antioxidants, antiwear agents, cetane improvers, corrosion inhibitors, demulsifiers, detergents, dispersants, flow improvers, lubricity agents, and metal deactivators. In other embodiments, the fuel additive can be embedded within a solid matrix.
- the matrix can be either hydrocarbon soluble or hydrocarbon insoluble. If the matrix material is hydrocarbon insoluble, the fuel must be able to penetrate the matrix and contact the fuel additive. It is disclosed to be particularly advantageous to embed a liquid fuel additive in a solid matrix. This is said to provide one means of controlling the rate the additive is released into fuel.
- thermoplastic material contains oil oxidation and acidification arresting additives and is positioned in a casing between a particle filtering material and a felt pad.
- the thermoplastic material can be high molecular weight polypropylene in the form of rice-shaped pellets, or spaghetti-shaped strands.
- the additives comprise about 10-17 weight % of the thermoplastic material/additive combination, and as the thermoplastic material is dissolved by above ambient temperature oil, the additives are released.
- High molecular weight polypropylene is described as superior for use as the thermoplastic material compared with polyester polycarbonates, polyallomer, polyethylene, and polysulfone, and ethylene propylene polypropylene is said to be particularly desirable.
- the invention provides a new process addressing the above needs with a solid dosing form of metallic combustion catalysts for fuels for combustors such as turbines, boilers, furnaces, process heaters, heat recovery units, diesel engines, and the like, utilizing carbonaceous, e.g., fossil, fuels such as distillate, residual and gaseous fuels.
- the invention provides, in one aspect, a material effective in preparing units for dosing small amounts of platinum and/or cerium into fuel by dissolution or diffusion according to the invention.
- the invention provides a catalytic metal additive concentrate (herein referred to as a CMAC) in nominally solid, semi-solid or viscous form.
- CMAC catalytic metal additive concentrate
- the invention also provides dosing units for simply and effectively supplying catalytic metal fuel additives to fuel in suitable low concentrations as are effective.
- the dosing units can be provided in suitable shapes, e.g., cylinders, cubes, spheres, or like shapes, to use with fuel filters, fuel/water separators or other devices made to contact diesel fuel as it is pumped to the engine or stored in the fuel tank or other part of the fuel system.
- a catalytic metal additive concentrate (herein referred to as a CMAC) is prepared and encapsulated with a solid polymer.
- CMAC catalytic metal additive concentrate
- Variations on this approach utilize the CMAC in various physical states including solid, semisolid or even highly viscous form.
- the encapsulation can be accomplished by embedding or dispersing the CMAC in a suitable polymer. Suitable polymers will provide structural integrity at the temperatures to be encountered and will release effective concentrations of the catalyst into the fuel under conditions of contact with the fuel. If desired, the CMAC can be dispersed in one polymer and then the resulting composite can be embedded in the same or a different polymer.
- the CMAC can be embedded in the polymer by mixing it with a polymer powder, melting the polymer while mixed with the CMAC, and solidifying the mixed polymer and CMAC in a desired shape.
- the fuel solubility characteristics of the polymer are chosen to define and limit the rate of additive release.
- the dosing units prepared in accord with the invention can supply a practically consistent additive application in the low ppm range to the fuel.
- a preferred physical form for the CMAC materials of the invention is in normally solid form.
- a dosing unit can comprise a semisolid (viscous to the point of resisting flow under its own weight) CMAC, which could be similarly held in contact with flowing fuel.
- the CMAC can be viscous and fully subject to flow and deformation at ambient temperatures.
- the additive application rate to the fuel can be controlled by a relatively high viscosity of the CMAC, which is maintained in very limited contact with fuel flow, e.g., in a by-pass region.
- the invention relates to a new process addressing the above needs by providing an improved method for preparing a dosing form of metallic combustion catalyst for fuels for combustors such as turbines, boilers, furnaces, process heaters, heat recovery units, diesel engines, and the like, utilizing carbonaceous, e.g., fossil, fuels such as distillate, residual and gaseous fuels.
- combustors such as turbines, boilers, furnaces, process heaters, heat recovery units, diesel engines, and the like
- carbonaceous e.g., fossil, fuels such as distillate, residual and gaseous fuels.
- a catalytic metal additive concentrate (herein referred to as a CMAC) is provided to aid in forming units for dosing small amounts of platinum and/or cerium into fuel by dissolution or diffusion. These dosing units enable simply and effectively supplying catalytic metal fuel additives to fuel in suitable low concentrations as are effective.
- dosing units for dosing small amounts of platinum and/or cerium into fuel by dissolution or diffusion can be prepared by encapsulating a CMAC with a suitable polymer.
- the CMAC can be in various physical states including solid, semisolid or even highly viscous form.
- the encapsulation can be accomplished by embedding or dispersing the CMAC in a suitable polymer.
- Suitable polymers will preferably provide structural integrity at the temperatures to be encountered and will release effective concentrations of the catalyst into the fuel under conditions of contact with the fuel. In some cases, simply wrapping the CMAC with a polymer film will be effective.
- the CMAC can be dispersed in one polymer and then the resulting composite can be embedded in the same or a different polymer.
- the CMAC can be embedded in the polymer by mixing it with a polymer powder, melting the polymer while mixed with the CMAC, and solidifying the mixed polymer and CMAC in a desired shape.
- the fuel solubility characteristics of the polymer would be chosen to define and limit the rate of additive release.
- the dosing units prepared in accord with the invention can supply a reasonably consistent additive application in the low ppm range to the fuel.
- a preferred physical form for the CMAC materials of the invention is in normally solid form.
- a dosing unit can comprise a semisolid (viscous to the point of resisting flow under its own weight) CMAC, which could be similarly held in contact with flowing fuel.
- the CMAC can be viscous and fully subject to flow and deformation at ambient temperatures.
- the additive application rate to the fuel can be controlled by a relatively high viscosity of the CMAC, which can be maintained in very limited contact with fuel flow, e.g., in a by-pass region.
- the dosing units supply catalytic metal fuel additives to fuel in suitable low concentrations as are effective.
- the dosing units can be provided in suitable shapes, e.g., cylinders, cubes, spheres, saddles or like shapes, to use with fuel filters, fuel/water separators or other devices made to contact diesel fuel as it is pumped to the engine or stored in the fuel tank or other part of the fuel system or special dosing apparatus.
- a CMAC is prepared in normally solid form and encapsulated with a solid polymer.
- normally solid as used herein we mean that preferred materials will be solid at temperatures of 50° C. and higher in that a one inch cube of material will substantially sustain its shape under its own weight at 20° C. for a the period of at least 60 minutes.
- Encapsulation can be accomplished by embedding or dispersing the CMAC in a suitable polymer. Suitable polymers will provide structural integrity at the temperatures to be encountered and will release effective concentrations of the catalyst into the fuel under conditions of contact with the fuel. If desired, the CMAC can be dispersed in one polymer and then the resulting composite can be embedded in the same or a different polymer.
- the CMAC can be embedded in the polymer by mixing it with a polymer powder, melting the polymer, allowing the mixture to solidify in a desired shape.
- the fuel solubility characteristics of the polymer would be chosen to define and limit the rate of additive release.
- the dosing units prepared in accord with the invention can supply a reasonably consistent additive application in the low ppm range (e.g., concentrations of ⁇ 20 ppm) to the fuel.
- a dosing unit can comprise a semisolid (viscous to the point of resisting flow under its own weight) CMAC, which could be similarly held in contact with flowing fuel.
- the additive fuel dosing rate would be controlled by a relatively high viscosity of the CMAC in very limited contact with fuel flow in a by-pass region.
- platinum COD also referred to herein as “COD-Pt-diphenyl”
- platinum COD also referred to herein as “COD-Pt-diphenyl”
- COD-Pt-diphenyl i.e., 1,5-cyclooctadiene platinum diphenyl
- Platinum acetylacetonate has a decomposition temperature of over 200° C.; however, it has very poor solubility in any solvent, only being about 0.5% soluble even in toluene and correspondingly less soluble in higher aromatic solvents. It is almost insoluble in aliphatics such as mineral spirits. Other suitable platinum compounds exhibit similar problems.
- the invention provides a method of preparing a solid dosing form of fuel additive, by: preparing a stable dispersion of platinum compound in a predetermined catalyst (e.g., a suitable Pt/Ce ratio) ratio in a solution of cerium (or other catalyst compound, such as one based on iron) soap, mixing the dispersion with a fuel-soluble polymer under conditions effective to uniformly distribute the dispersion within the polymer; and forming the polymer into a predetermined shape.
- a predetermined catalyst e.g., a suitable Pt/Ce ratio
- cerium or other catalyst compound, such as one based on iron
- the noted stable dispersion of platinum compound ha a predetermined Pt/Ce ratio in a solution of cerium soap (or other catalysts), can be prepared by adding a designated platinum compound as a solid or otherwise to the cerium soap solution and milling in a ball mill or other suitable particle mill to reduce the solids to small particles that permit the formation of a stable dispersion.
- the soaps present in the cerium soap solution disperse the solid platinum compound particles and prevent agglomeration and subsequent loss of stability. Additional dispersant, can be added if necessary.
- oleic acid There are many of these known to the art but one of the most suitable is oleic acid. Others include amphoterics such as oleyl imidazolines and the like. Where the amounts of oleates in the catalyst metal concentrates are high enough, Such additions are not necessary.
- solvent evaporation will accomplish at least two further goals: to further concentrate the additive package and increase the viscosity of the resulting solution to levels where complete dispersion stability is achieved. This also removes the low boiling solvents that can be troublesome. Solvent evaporation, in combination with suitable processing, can result in a final additive concentrate that is up to about 50% cerium and 1% or more platinum (both as metal basis) ha a liquid, usable form. These are very high concentrations for catalyst metals of the type concerned.
- the noted stable dispersions can also be formed by adding a platinum compound to the soap as a solution, usually in a light carrier such as toluene, and evaporating the light carrier along, with the light components ha the solvent evaporation step. This results in the precipitation of small particles of solid platinum compound dispersed in the cerium soap solution. These can then be milled or not depending on the degree of stability required.
- the invention provides a method of preparing, a solid dosing form of fuel additive, by: preparing a solution of a platinum composition including a typical low-boiling solvent including a sufficient amount of high-boiling solvent to retain fluidity of the composition in the absence of the low-boiling solvent; evaporating the low-boiling solvent to prepare a viscous catalyst solution; mixing the viscous catalyst solution with a fuel-soluble polymer under conditions effective to uniformly distribute the dispersion within the polymer; and forming the polymer into a predetermined shape.
- the polymer used to mix with the platinum and other catalyst dispersion or solution as noted above will be one of those, such as from the patents cited above, which is soluble in the fuel at a degree sufficient to release the additive to the fuel.
- Polymers based on olefins e.g., polyethylene, polypropylene, and copolymers of ethylene and propylene, can be used with good effect.
- a solvent is used to dissolve the catalyst composition for mixing with a polymer for processing in melt form
- both the catalyst composition and the solvent have properties which assure their survival in a suitable form.
- Catalysts are described below.
- Solvents of the hydrocarbon type are suitable where they are either of suitably high boiling point initially or evaporated to be freed of low boiling components. Preferred boiling points for solvents will be over 100° C., and preferably over 150° C. Specific examples are given below.
- the polymer and the CMAC can be blended at any suitable ratio to give the desired release rate when placed in contact with the fuel under the conditions of operation.
- ratios of CMAC to polymer should be at a ratio of from about 3:1 to about 1:100, typically from about 1:1 to about 1:10.
- concentration of metal within the blend will desirably be within the range of from about 10 to about 600 mg metal to gram of blend, more narrowly from about 300 to about 500 mg metal to gram of blend.
- One test of the suitability of the blend is to place a 1 cm 3 cube of the blend in 1 liter of fuel for 1 hour and measure the concentration of metal in the fuel.
- the preferred blends of polymer and CMAC materials will equilibrate at levels within the desired dosage rates given below.
- the blends of polymer and CMAC materials are shaped typically by heating, e.g., at an elevated temperature of from about 150° C. to about 300° C., and molding. Preferred polymers will melt or soften at temperatures within this range.
- a mixture of polymer with a CMAC is shaped by a suitable molding or other forming technique, e.g., compression molding, injection molding, extrusion, or the like.
- the blends of polymer and CMAC materials can be enveloped in a suitable polymer film which can be permeated by the fuel and permit leaching into the fuel at a controlled rate.
- Typical of the films are ABS, polyalkenes, polyalcohols like polyvinyl alcohol, polyesters like polyvinyl acetate, and other polymers having similar permeabilities or which can be formed with similar permeabilities for the fuel in question.
- the preferred polymers include those that can be applied by dipping, coextrusion or simple lamination techniques.
- any suitable fuel can be treated with a CMAC prepared in accord with the invention. It can be one or a blend of fuels selected from the group consisting of distillate fuels, including diesel fuel, e.g., No. 2 Diesel fuel, gasoline, jet fuel, e.g., Jet A, or the like, and biologically-derived fuels, such as those comprising a “mono-alkyl ester-based oxygenated fuel”, i.e., fatty acid esters, preferably methyl esters of fatty acids derived from triglycerides, e.g., soybean oil, Canola oil and/or tallow.
- Other hydrocarbons, including liquids and gases, e.g., natural gas, or fuels derived from gas and/or emulsion components can be employed.
- Cerium and/or iron catalyst levels can be dosed into the fuels at fairly uniform levels to provide concentrations in the fuel of as low as 0.05 ppm and platinum levels can be as low as 0.0005 ppm.
- the process of the invention employs a fuel-soluble, multi-metal catalyst, preferably comprising fuel-soluble platinum and either cerium or iron.
- the cerium or iron are typically dosed in amounts sufficient to provide concentrations in the fuel of from 0.5 to 25 ppm and the platinum from 0.0005 to 2 ppm, with preferred fuel concentrations of cerium and/or iron of from 5 to 10 ppm, e.g., 7.5 ppm, and the platinum from 0.05 to 0.5 ppm, e.g., 0.15 ppm.
- a preferred ratio of cerium and/or iron to platinum is from 75:1 to 10:1.
- One narrower range is from 60:1 to 25:1.
- the fuel treated with a CMAC of the invention can contain detergent (e.g., 50-300 ppm), lubricity additive (e.g., 25 to about 500 ppm), other additives, and suitable fuel-soluble catalyst metal compositions, e.g., 0.1-2 ppm fuel soluble platinum group metal composition, e.g., platinum COD or platinum acetylacetonate and/or 2-20 ppm fuel soluble cerium or iron composition, e.g., cerium, cerium octoate, ferrocene, iron oleate, iron octoate and the like.
- detergent e.g., 50-300 ppm
- lubricity additive e.g., 25 to about 500 ppm
- suitable fuel-soluble catalyst metal compositions e.g., 0.1-2 ppm fuel soluble platinum group metal composition, e.g., platinum COD or platinum acetylacetonate and/or 2-20 ppm fuel soluble cerium or iron composition,
- a combination of platinum with either iron or cerium at low concentrations in fuels is as effective as much higher concentrations of cerium, iron or other metals without platinum in reducing carbon or soot deposits or emissions. Concentrations of a few ppm metals in combination are as effective as 30-100 ppm of iron and/or cerium used alone.
- the metal concentration in the fuel achieved by using the CMAC formulations of the invention avoid problems often encountered using traditional levels of cerium or iron, which are high enough to be factors in causing equipment fouling due to the high ash burden associated with high metal concentrations in the fuel.
- the preferred bimetallic and trimetallic platinum and other catalyst metal combinations are compatible with standard additive components for distillate and residual fuels such as pour point reducers, antioxidant, corrosion inhibitors and the like.
- cerium III acetylacetonate cerium III napthenate
- cerium octoate cerium oleate and other soaps such as stearate, neodecanoate, and octoate (2-ethylhexoate).
- the cerium is preferred at concentrations of 1 to 15 ppm cerium w/v of fuel.
- Fatty acid containing compounds of this type are known to the art as soaps.
- the cerium is supplied as cerium hydroxy oleate propionate complex (diluted with light mineral spirits to 40% cerium by weight). Preferred levels are toward the lower end of this range, e.g., less than 8 ppm.
- iron compounds include ferrocene, ferric and ferrous acetylacetonates, iron soaps like octoate and stearate (commercially available as Fe(III) compounds, usually), iron pentacarbonyl Fe(CO) 5 , iron napthenate, and iron tallate.
- platinum group metal compositions e.g., 1,5-cyclooctadiene platinum diphenyl (platinum COD, also referred to as “COD-Pt-diphenyl”), described in U.S. Pat. No. 4,891,050 to Bowers, et al., U.S. Pat. No. 5,034,020 to Epperly, et al., and U.S. Pat. No. 5,266,093 to Peter-Hoblyn, et al., can be employed as the platinum source.
- platinum COD platinum COD
- COD-Pt-diphenyl platinum COD
- platinum group metal catalyst compositions include commercially-available or easily-synthesized platinum group metal acetylacetonates, platinum group metal dibenzylidene acetonates, and fatty acid soaps of tetramine platinum metal complexes, e.g., tetramine platinum oleate.
- the combustion of a fuel treated according to the invention can be of an emulsion with water, wherein an oil phase is emulsified with water, the water comprising from 1 to 30% water based on the weight of the distillate fuel, residual fuel, aviation kerosene or the like.
- the emulsion will be predominantly of the water-in-oil type and will preferably contain surfactants, lubricity additives and/or corrosion inhibitors in addition to the other components mentioned above.
- surfactants lubricity additives and/or corrosion inhibitors in addition to the other components mentioned above.
- the additives introduced into, the fuel in accord with the invention can improve combustion efficiency and reduce particulates without the use of oxidation catalysts or particulate filters for enhanced emissions control on diesel engines. Also, better carbon burn out in open flame combustion sources will lead to lower carbon deposits on heat transfer surfaces and lower soot oxidation temperatures on downstream heat recovery devices.
- This example describes the preparation of a solid CMAC according to the invention containing a cerium catalyst composition.
- Two hundred grains of cerium hydroxy oleate propionate complex (diluted with light mineral spirits to 40% cerium by weight), was mixed with 40 grams of heavy mineral oil and charged into a 500 ml vacuum distillation apparatus.
- the flask was immersed in an oil bath with temperature control. Vacuum was applied using a water eductor mechanism and the oil bath temperature slowly increased. After about an hour, the temperature reached 125° C. and the distillation was stopped, the flask was reweighed and the resulting weight after processing indicated that 50.46 grains of solvent had distilled over to the receiver.
- the resulting concentrate was calculated to have a cerium metal concentration of 42% by weight.
- a small beaker of material produced was heated on a hot plate and the boiling point was found to be over 175° C. and suitable for processing temperatures encountered with polymers of the type employed in the invention to provide slow release fuel additive substrates.
- This example describes the preparation of a solid CMAC according to the invention containing both platinum and cerium catalyst compositions at a 50:1 weight ratio of cerium to platinum.
- To 200 grains of cerium hydroxy oleate propionate complex (diluted with light mineral spirits to 40% cerium) is added 3.2 grams of solid platinum acetylacetonate and the materials are ball milled overnight, to produce a semi-stable dispersion of platinum acetylacetonate in the cerium concentrate.
- the resulting mixture is then further mixed with 40 grams of heavy mineral oil and charged into a 500 ml vacuum distillation apparatus.
- the flask is immersed in an oil bath with temperature control and vacuum is applied using, a water eductor mechanism and the oil bath temperature slowly increased. Processing is completed as in Example 1.
- This example describes the preparation of a CMAC according to the invention containing both platinum and cerium catalyst compositions at a 50:1 weight ratio of cerium to platinum.
- 310 grains of 40% cerium concentrate was charged to a 1-liter ball mill with ceramic media.
- 5.0 grams of platinum acetylacetonate was added to the mill and the mill sealed.
- the mixture was ball milled overnight, producing a semi-stable dispersion of platinum acetylacetonate in the cerium concentrate.
- the resultant mixture slowly (over an hour or two) deposited a small amount of solid platinum compound on the bottom of the container.
- a total of 288.7 grains was recovered from the ball mill and transferred to a 500 ml round bottom flask.
- Example 5 This example repeats the procedure of Example 4, but employs added oleic acid as a dispersant in replacement for the heavy mineral oil. Processing is otherwise essentially the same.
- This example describes the preparation of another CMAC according to the invention containing cerium catalyst composition.
- Two hundred grams of 40% cerium concentrate was mixed with 60 grains of heavy mineral oil and charged into a 500 ml vacuum distillation apparatus. The flask was immersed in an oil bath with temperature control. Vacuum was applied using a water eductor mechanism and the oil bath temperature slowly increased. After 90 minutes, the temperature reached 160° C. and the distillation was stopped, the flask was reweighed and the resulting weight indicated that 54.84 grams of solvent had distilled over to the receiver. The resulting concentrate was calculated to have a cerium metal concentration of 39% wt. The result of this process was suitable for processing temperatures of 175° C. with high melting polymers and had a lower viscosity than Example 1, making it easier to work into a polymer powder.
- This example describes the preparation of a semisolid CMAC according to the invention containing both platinum and cerium catalyst compositions at a 50:1 weight ratio of cerium to platinum.
- platinum compound solutions in suitable solvents are added to a mixture of cerium catalyst material and solvents (as in Example 4) in the distillation apparatus.
- 80 grams of Platinum Plus 3100-SC, a 4.7% solution of COD-Pt-diphenyl in toluene, are added.
- the final processing temperatures is maintained below 100° C. to avoid the decomposition into platinum metal in the matrix.
- This example describes the preparation of a semisolid CMAC according to the invention as set out in Example 7, but employs platinum acetylacetonate in place of the COD-Pt-diphenyl, and the temperature is maintained at less than 250° C.
- Example 7 The procedure of Example 7 is repeated but this time the ratio of platinum:cerium is 1:15, obtained by increasing the amount of platinum compound in the composition proportionately.
- This example describes the preparation of another CMAC according to the invention containing cerium catalyst composition.
- Two hundred grams of 40% cerium concentrate was mixed with 100 grains of heavy mineral oil and charged into a 500 ml vacuum distillation apparatus.
- the flask was immersed in an oil bath with temperature control. Vacuum was applied using a water eductor mechanism and the oil bath temperature slowly increased. After 90 minutes, the temperature reached 160° C. and the distillation was stopped, the flask was reweighed and the resulting weight indicated that about 55 grams of solvent had distilled over to the receiver.
- the resulting concentrate was calculated to have a cerium metal concentration of 32% wt.
- the result of this process was suitable for processing temperatures of 175° C. with high melting polymers and had a lower viscosity than Example 1, making it easier to work into a polymer powder.
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- Catalysts (AREA)
Abstract
Delivery of metallic combustion catalysts to internal combustion engines and other combustion devices is improved by dosing units that have the ability to effect the slow and positive supply of metallic additives, including platinum and/or cerium containing catalyst compositions, to fuel. The invention provides additive dosing materials and methods for simply and effectively supplying catalytic metal fuel additives to fuel in suitable low concentrations as are effective. The dosing units can be used with devices made to contact diesel fuel. In one approach, a catalytic metal additive concentrate (CMAC) is prepared in normally solid, semisolid or viscous form. The CMAC will preferably be encapsulated with a solid polymer. The encapsulation can be accomplished by embedding or dispersing the CMAC in a suitable polymer. If desired, the CMAC can be dispersed in one polymer and then the resulting composite can be embedded in the same or a different polymer. In an alternative form, a dosing unit can comprise a semisolid CMAC, which could be similarly held in contact with flowing fuel.
Description
- This application claims priority to prior U.S. Provisional Patent Application S. No. 60/366,860, filed Mar. 22, 2002.
- The invention concerns a new process for improving the delivery of metallic combustion catalysts to internal combustion engines and other combustion devices and to enable the production of additive delivery means which have the ability to effect the slow and positive supply of metallic additives, including platinum containing catalyst compositions, to fuel. The also invention provides additive release materials and methods designed for compatibility with various on-board delivery mechanisms.
- A number of approaches have been utilized to deliver fuel additives to combustors such as internal combustion engines. Some additive delivery means require the use of highly concentrated catalyst mixtures with low volatility or high viscosity solvent carriers. Platinum and other catalyst metal components are not freely soluble or fully stable in forms compatible with some mechanisms used to achieve their slow release into fuels due to poor solubility in heavy solvents.
- In U.S. Pat. No. 4,662,327, Sprugel, et al., disclose metering a liquid additive continuously into a fuel supply line. This liquid type delivery device has been viewed as complex and possessed of other disadvantages, leading to the development of devices based on solid, soluble additive materials.
- In another system, Davis discloses a dissolvable element in U.S. Pat. No. 5,507,942. He provides a fuel filter assembly including a fuel additive element formed into a hollow cylindrical dissolvable insert comprising fuel additive in a wax substrate. In a preferred form, the fuel additive comprises a microbiocide that is compatible with combustion systems and fuels and which is more soluble in fuel than water. The microbiocide is encapsulated in the wax substrate, which has a high melting point and a burning characteristic for proper release of the microbiocide without compromising exhaust gas emissions and without unduly releasing an excessive amount of fuel additive that may adversely affect engine and fuel components. The fuel additive may also comprise cetane improvers, antioxidants, stabilizers, combustion improvers and emission reducers. The wax substrate is fabricated from a paraffin, which is said to be a hydrocarbon mixture with clean burning characteristics. The insert is housed within the hollow cylinder of a fuel filter canister. It is supported in a vertical orientation and slowly releases the fuel additive upon dissolving the wax substrate.
- In U.S. Pat. No. 6,238,554, to Martin, Jr., et al., a fuel filter is described including a fuel additive that can be released into fuel. The rate of release for the fuel is said to be controlled to a substantially constant rate to maintain a uniform level of fuel additive in the fuel. Fuel from a filter chamber migrates through a diffusion orifice into an inner chamber and contacts an additive tablet which can have an outer coating. Fuel diffuses through the coating to contact a fuel additive composition, which dissolves in the fuel to provide a fuel composition comprising the dissolved additive. The fuel composition diffuses back through the coating into the inner chamber where it mixes with fuel. The fuel additives can be liquid or solid, and two or more fuel additives can be combined and can be compounded with a suitable polymer. They can be either a solid or semisolid material in a form, such as tablet, to control the rate of release of the additive into the fuel. The fuel additive can further include a wide variety of binders, compounding agents and mold release agents. When the additive is provided in liquid form, it is preferably combined with a suitable agent to form a solid or semisolid material. The term fuel additive includes antioxidants, antiwear agents, cetane improvers, corrosion inhibitors, demulsifiers, detergents, dispersants, flow improvers, lubricity agents, and metal deactivators. In other embodiments, the fuel additive can be embedded within a solid matrix. The matrix can be either hydrocarbon soluble or hydrocarbon insoluble. If the matrix material is hydrocarbon insoluble, the fuel must be able to penetrate the matrix and contact the fuel additive. It is disclosed to be particularly advantageous to embed a liquid fuel additive in a solid matrix. This is said to provide one means of controlling the rate the additive is released into fuel.
- In U.S. Pat. No. 5,591,330, Lefebvre describes an oil filter containing an oil-soluble thermoplastic additive material. The thermoplastic material contains oil oxidation and acidification arresting additives and is positioned in a casing between a particle filtering material and a felt pad. The thermoplastic material can be high molecular weight polypropylene in the form of rice-shaped pellets, or spaghetti-shaped strands. The additives comprise about 10-17 weight % of the thermoplastic material/additive combination, and as the thermoplastic material is dissolved by above ambient temperature oil, the additives are released. High molecular weight polypropylene is described as superior for use as the thermoplastic material compared with polyester polycarbonates, polyallomer, polyethylene, and polysulfone, and ethylene propylene polypropylene is said to be particularly desirable.
- In U.S. Pat. No. 4,075,098, Paul, et al., describe an oil filter containing a body of an oil soluble, relatively solid polymer having oil additives compounded therein. They note that virtually any polymer with desired properties may be used in practice in their system such as ethylene-propylene copolymers ranging in molecular weight from 200,000 to 300,000; ethylene-ethylacrylate polymers ranging in molecular weight from 200,000 to 300,000; polypropylene oxide having a molecular weight of about 500,000; and ethylene-vinyl acetate copolymer ranging in molecular weight from 200,000 to 300,000. One polymer described as highly satisfactory is polyisobutylene ranging in molecular weight from approximately 60,000 to 135,000. Similarly, in U.S. Pat. No. 3,336,223, Kneeland describes an oil filter having a polymeric insert carrying oil additives. The additives are incorporated into the oil as the polymer slowly dissolves.
- In U.S. Pat. No. 5,456,217, to Thunker, et al., a device is described for direct addition of solid additives, such as ferrocene, to fuels for internal combustion engines. A solid additive is held in a replaceable cartridge, which is located in a portion of the filling neck of a fuel tank. Fuel filled through the neck dissolves the additive into the fuel.
- The art does not describe or enable the preparation of platinum and/or cerium based fuel additive dosing units that can be used to controllably release platinum and/or cerium combustion catalysts into fuel in very low amounts by dissolution or diffusion.
- Accordingly, there is a present need for a practical method of making a solid dosing form of platinum and/or cerium and/or iron combustion catalyst, the resulting additive composition and practical system for dosing fuels using it.
- The invention provides a new process addressing the above needs with a solid dosing form of metallic combustion catalysts for fuels for combustors such as turbines, boilers, furnaces, process heaters, heat recovery units, diesel engines, and the like, utilizing carbonaceous, e.g., fossil, fuels such as distillate, residual and gaseous fuels.
- The invention provides, in one aspect, a material effective in preparing units for dosing small amounts of platinum and/or cerium into fuel by dissolution or diffusion according to the invention. In this aspect the invention provides a catalytic metal additive concentrate (herein referred to as a CMAC) in nominally solid, semi-solid or viscous form.
- The invention also provides dosing units for simply and effectively supplying catalytic metal fuel additives to fuel in suitable low concentrations as are effective. The dosing units can be provided in suitable shapes, e.g., cylinders, cubes, spheres, or like shapes, to use with fuel filters, fuel/water separators or other devices made to contact diesel fuel as it is pumped to the engine or stored in the fuel tank or other part of the fuel system.
- In one approach for preparing dosing units for dosing small amounts of platinum and/or cerium into fuel by dissolution or diffusion according to the invention, a catalytic metal additive concentrate (herein referred to as a CMAC) is prepared and encapsulated with a solid polymer. Variations on this approach utilize the CMAC in various physical states including solid, semisolid or even highly viscous form. The encapsulation can be accomplished by embedding or dispersing the CMAC in a suitable polymer. Suitable polymers will provide structural integrity at the temperatures to be encountered and will release effective concentrations of the catalyst into the fuel under conditions of contact with the fuel. If desired, the CMAC can be dispersed in one polymer and then the resulting composite can be embedded in the same or a different polymer.
- In some cases, the CMAC can be embedded in the polymer by mixing it with a polymer powder, melting the polymer while mixed with the CMAC, and solidifying the mixed polymer and CMAC in a desired shape. The fuel solubility characteristics of the polymer are chosen to define and limit the rate of additive release. The dosing units prepared in accord with the invention can supply a practically consistent additive application in the low ppm range to the fuel.
- A preferred physical form for the CMAC materials of the invention is in normally solid form. In one alternative form, a dosing unit can comprise a semisolid (viscous to the point of resisting flow under its own weight) CMAC, which could be similarly held in contact with flowing fuel. Also, the CMAC can be viscous and fully subject to flow and deformation at ambient temperatures. If desired, the additive application rate to the fuel can be controlled by a relatively high viscosity of the CMAC, which is maintained in very limited contact with fuel flow, e.g., in a by-pass region.
- The processes for preparing these products and their use in additive dosing systems which causes dissolution of the catalyst dosing units, are also provided.
- Many of the preferred aspects of the invention are described below. Equivalent compositions are contemplated.
- The invention relates to a new process addressing the above needs by providing an improved method for preparing a dosing form of metallic combustion catalyst for fuels for combustors such as turbines, boilers, furnaces, process heaters, heat recovery units, diesel engines, and the like, utilizing carbonaceous, e.g., fossil, fuels such as distillate, residual and gaseous fuels.
- In one aspect, a catalytic metal additive concentrate (herein referred to as a CMAC) is provided to aid in forming units for dosing small amounts of platinum and/or cerium into fuel by dissolution or diffusion. These dosing units enable simply and effectively supplying catalytic metal fuel additives to fuel in suitable low concentrations as are effective.
- Preferably, dosing units for dosing small amounts of platinum and/or cerium into fuel by dissolution or diffusion according to the invention, can be prepared by encapsulating a CMAC with a suitable polymer. The CMAC can be in various physical states including solid, semisolid or even highly viscous form. The encapsulation can be accomplished by embedding or dispersing the CMAC in a suitable polymer. Suitable polymers will preferably provide structural integrity at the temperatures to be encountered and will release effective concentrations of the catalyst into the fuel under conditions of contact with the fuel. In some cases, simply wrapping the CMAC with a polymer film will be effective. If desired, the CMAC can be dispersed in one polymer and then the resulting composite can be embedded in the same or a different polymer.
- In some cases, the CMAC can be embedded in the polymer by mixing it with a polymer powder, melting the polymer while mixed with the CMAC, and solidifying the mixed polymer and CMAC in a desired shape. The fuel solubility characteristics of the polymer would be chosen to define and limit the rate of additive release. The dosing units prepared in accord with the invention can supply a reasonably consistent additive application in the low ppm range to the fuel.
- A preferred physical form for the CMAC materials of the invention is in normally solid form. In one alternative form, a dosing unit can comprise a semisolid (viscous to the point of resisting flow under its own weight) CMAC, which could be similarly held in contact with flowing fuel. Also, the CMAC can be viscous and fully subject to flow and deformation at ambient temperatures. If desired, the additive application rate to the fuel can be controlled by a relatively high viscosity of the CMAC, which can be maintained in very limited contact with fuel flow, e.g., in a by-pass region.
- The dosing units supply catalytic metal fuel additives to fuel in suitable low concentrations as are effective. The dosing units can be provided in suitable shapes, e.g., cylinders, cubes, spheres, saddles or like shapes, to use with fuel filters, fuel/water separators or other devices made to contact diesel fuel as it is pumped to the engine or stored in the fuel tank or other part of the fuel system or special dosing apparatus.
- In one approach for preparing dosing units for dosing small amounts of platinum and/or cerium into fuel by dissolution or diffusion according to the invention, a CMAC is prepared in normally solid form and encapsulated with a solid polymer. By the tern “normally solid” as used herein we mean that preferred materials will be solid at temperatures of 50° C. and higher in that a one inch cube of material will substantially sustain its shape under its own weight at 20° C. for a the period of at least 60 minutes. Encapsulation can be accomplished by embedding or dispersing the CMAC in a suitable polymer. Suitable polymers will provide structural integrity at the temperatures to be encountered and will release effective concentrations of the catalyst into the fuel under conditions of contact with the fuel. If desired, the CMAC can be dispersed in one polymer and then the resulting composite can be embedded in the same or a different polymer.
- In some cases the CMAC can be embedded in the polymer by mixing it with a polymer powder, melting the polymer, allowing the mixture to solidify in a desired shape. The fuel solubility characteristics of the polymer would be chosen to define and limit the rate of additive release. The dosing units prepared in accord with the invention can supply a reasonably consistent additive application in the low ppm range (e.g., concentrations of <20 ppm) to the fuel.
- In an alternative form, a dosing unit can comprise a semisolid (viscous to the point of resisting flow under its own weight) CMAC, which could be similarly held in contact with flowing fuel. Here, the additive fuel dosing rate would be controlled by a relatively high viscosity of the CMAC in very limited contact with fuel flow in a by-pass region.
- Normally-encountered solvents for additive components such as toluene, light mineral spirits and kerosene have too low a boiling point for normally solid CMAC containing dosing units. Moreover, they have too low a viscosity for the semisolid CMAC containing dosing units. Importantly, they will enable too low metal solubility for good application of either the solid or semisolid CMAC's. These normal solvents can prevent the formation of suitably high additive concentrations, as they exhibit solubility limits, especially for suitable platinum compounds, that are quite low. Some of these conventional solvents have the ability to dissolve only a few tenths of a percent of an active metal containing composition. This is true even of toluene, which is an especially good solvent. The mere addition of solid platinum compound to either a solid or semisolid CMAC, will result in a composition that is unstable and which will not deliver fuel borne catalyst (FBC) in uniform concentrations to the combustor and downstream components, resulting in erratic performance of the additive due to a highly fluctuating metal (especially Pt) concentration in the fuel.
- In addition to these problems, decomposition points of the most soluble forms of platinum are too low to allow the use of some of the most favored polymers in the preparation of solid CMAC's. In this regard, it is noted that platinum COD (also referred to herein as “COD-Pt-diphenyl”), i.e., 1,5-cyclooctadiene platinum diphenyl, described in U.S. Pat. No. 4,891,050 to Bowers, et al., U.S. Pat. No. 5,034,020 to Epperly, et al., and U.S. Pat. No. 5,266,093 to Peter-Hoblyn, et al., decomposes at about 200° F. The disclosures of these patents are hereby incorporated by reference. Thus, dispersing COD-Pt-diphenyl in one preferred polymer melting at 150-200° C. (say, 350° F. or so) would result in destruction of the Pt complex with the resultant formation of platinum metal. This would also result in a highly nonuniform application of platinum to the system.
- Not all fuel-soluble platinum materials decompose under these conditions, but their use can still present severe practical problems. Platinum acetylacetonate has a decomposition temperature of over 200° C.; however, it has very poor solubility in any solvent, only being about 0.5% soluble even in toluene and correspondingly less soluble in higher aromatic solvents. It is almost insoluble in aliphatics such as mineral spirits. Other suitable platinum compounds exhibit similar problems.
- In one aspect, the invention provides a method of preparing a solid dosing form of fuel additive, by: preparing a stable dispersion of platinum compound in a predetermined catalyst (e.g., a suitable Pt/Ce ratio) ratio in a solution of cerium (or other catalyst compound, such as one based on iron) soap, mixing the dispersion with a fuel-soluble polymer under conditions effective to uniformly distribute the dispersion within the polymer; and forming the polymer into a predetermined shape.
- The noted stable dispersion of platinum compound ha a predetermined Pt/Ce ratio in a solution of cerium soap (or other catalysts), can be prepared by adding a designated platinum compound as a solid or otherwise to the cerium soap solution and milling in a ball mill or other suitable particle mill to reduce the solids to small particles that permit the formation of a stable dispersion. The soaps present in the cerium soap solution disperse the solid platinum compound particles and prevent agglomeration and subsequent loss of stability. Additional dispersant, can be added if necessary. There are many of these known to the art but one of the most suitable is oleic acid. Others include amphoterics such as oleyl imidazolines and the like. Where the amounts of oleates in the catalyst metal concentrates are high enough, Such additions are not necessary.
- This procedure results in a stable or semi-stable dispersion without further processing. However, solvent evaporation will accomplish at least two further goals: to further concentrate the additive package and increase the viscosity of the resulting solution to levels where complete dispersion stability is achieved. This also removes the low boiling solvents that can be troublesome. Solvent evaporation, in combination with suitable processing, can result in a final additive concentrate that is up to about 50% cerium and 1% or more platinum (both as metal basis) ha a liquid, usable form. These are very high concentrations for catalyst metals of the type concerned.
- The noted stable dispersions can also be formed by adding a platinum compound to the soap as a solution, usually in a light carrier such as toluene, and evaporating the light carrier along, with the light components ha the solvent evaporation step. This results in the precipitation of small particles of solid platinum compound dispersed in the cerium soap solution. These can then be milled or not depending on the degree of stability required.
- In another aspect, the invention provides a method of preparing, a solid dosing form of fuel additive, by: preparing a solution of a platinum composition including a typical low-boiling solvent including a sufficient amount of high-boiling solvent to retain fluidity of the composition in the absence of the low-boiling solvent; evaporating the low-boiling solvent to prepare a viscous catalyst solution; mixing the viscous catalyst solution with a fuel-soluble polymer under conditions effective to uniformly distribute the dispersion within the polymer; and forming the polymer into a predetermined shape.
- In this case, mineral oil and other high boiling aliphatics are preferred because the normal platinum compounds are poorly soluble in them. The use of more soluble solvent systems would actually be detrimental as these promote crystal growth and dissolution of the solid dispersed phase, resulting in degradation of the dispersion. Inorganic forms of platinum could also be used, but the resulting cake or liquid would release a stream of fine particles of platinum compound rather than dissolved forms. This will be acceptable if the particle size is small enough to prevent settling out in other parts of the system, filter plugging and injector failure. Accordingly, extremely small, highly milled dispersed particles of platinum oxide or similar compounds are contemplated.
- The polymer used to mix with the platinum and other catalyst dispersion or solution as noted above, will be one of those, such as from the patents cited above, which is soluble in the fuel at a degree sufficient to release the additive to the fuel. Polymers based on olefins, e.g., polyethylene, polypropylene, and copolymers of ethylene and propylene, can be used with good effect. In embodiments where a solvent is used to dissolve the catalyst composition for mixing with a polymer for processing in melt form, both the catalyst composition and the solvent have properties which assure their survival in a suitable form. Catalysts are described below. Solvents of the hydrocarbon type are suitable where they are either of suitably high boiling point initially or evaporated to be freed of low boiling components. Preferred boiling points for solvents will be over 100° C., and preferably over 150° C. Specific examples are given below.
- The polymer and the CMAC can be blended at any suitable ratio to give the desired release rate when placed in contact with the fuel under the conditions of operation. Typically, ratios of CMAC to polymer should be at a ratio of from about 3:1 to about 1:100, typically from about 1:1 to about 1:10. The concentration of metal within the blend will desirably be within the range of from about 10 to about 600 mg metal to gram of blend, more narrowly from about 300 to about 500 mg metal to gram of blend. One test of the suitability of the blend is to place a 1 cm3 cube of the blend in 1 liter of fuel for 1 hour and measure the concentration of metal in the fuel. The preferred blends of polymer and CMAC materials will equilibrate at levels within the desired dosage rates given below.
- The blends of polymer and CMAC materials are shaped typically by heating, e.g., at an elevated temperature of from about 150° C. to about 300° C., and molding. Preferred polymers will melt or soften at temperatures within this range. Typically, a mixture of polymer with a CMAC is shaped by a suitable molding or other forming technique, e.g., compression molding, injection molding, extrusion, or the like. If desired, for some applications, the blends of polymer and CMAC materials can be enveloped in a suitable polymer film which can be permeated by the fuel and permit leaching into the fuel at a controlled rate. Typical of the films are ABS, polyalkenes, polyalcohols like polyvinyl alcohol, polyesters like polyvinyl acetate, and other polymers having similar permeabilities or which can be formed with similar permeabilities for the fuel in question. The preferred polymers include those that can be applied by dipping, coextrusion or simple lamination techniques.
- As required by a particular process or combustor, any suitable fuel can be treated with a CMAC prepared in accord with the invention. It can be one or a blend of fuels selected from the group consisting of distillate fuels, including diesel fuel, e.g., No. 2 Diesel fuel, gasoline, jet fuel, e.g., Jet A, or the like, and biologically-derived fuels, such as those comprising a “mono-alkyl ester-based oxygenated fuel”, i.e., fatty acid esters, preferably methyl esters of fatty acids derived from triglycerides, e.g., soybean oil, Canola oil and/or tallow. Other hydrocarbons, including liquids and gases, e.g., natural gas, or fuels derived from gas and/or emulsion components can be employed.
- Cerium and/or iron catalyst levels can be dosed into the fuels at fairly uniform levels to provide concentrations in the fuel of as low as 0.05 ppm and platinum levels can be as low as 0.0005 ppm.
- The process of the invention employs a fuel-soluble, multi-metal catalyst, preferably comprising fuel-soluble platinum and either cerium or iron. The cerium or iron are typically dosed in amounts sufficient to provide concentrations in the fuel of from 0.5 to 25 ppm and the platinum from 0.0005 to 2 ppm, with preferred fuel concentrations of cerium and/or iron of from 5 to 10 ppm, e.g., 7.5 ppm, and the platinum from 0.05 to 0.5 ppm, e.g., 0.15 ppm. A preferred ratio of cerium and/or iron to platinum is from 75:1 to 10:1. One narrower range is from 60:1 to 25:1.
- The fuel treated with a CMAC of the invention can contain detergent (e.g., 50-300 ppm), lubricity additive (e.g., 25 to about 500 ppm), other additives, and suitable fuel-soluble catalyst metal compositions, e.g., 0.1-2 ppm fuel soluble platinum group metal composition, e.g., platinum COD or platinum acetylacetonate and/or 2-20 ppm fuel soluble cerium or iron composition, e.g., cerium, cerium octoate, ferrocene, iron oleate, iron octoate and the like.
- A combination of platinum with either iron or cerium at low concentrations in fuels is as effective as much higher concentrations of cerium, iron or other metals without platinum in reducing carbon or soot deposits or emissions. Concentrations of a few ppm metals in combination are as effective as 30-100 ppm of iron and/or cerium used alone. The metal concentration in the fuel achieved by using the CMAC formulations of the invention avoid problems often encountered using traditional levels of cerium or iron, which are high enough to be factors in causing equipment fouling due to the high ash burden associated with high metal concentrations in the fuel.
- The preferred bimetallic and trimetallic platinum and other catalyst metal combinations are compatible with standard additive components for distillate and residual fuels such as pour point reducers, antioxidant, corrosion inhibitors and the like.
- Among the specific cerium compounds are: cerium III acetylacetonate, cerium III napthenate, and cerium octoate, cerium oleate and other soaps such as stearate, neodecanoate, and octoate (2-ethylhexoate). Many of the cerium compounds are trivalent compounds meeting the formula: Ce (OOCR)3 wherein R=hydrocarbon, preferably C2 to C22, and including aliphatic, alicyclic, aryl and alkylaryl. The cerium is preferred at concentrations of 1 to 15 ppm cerium w/v of fuel. Fatty acid containing compounds of this type are known to the art as soaps. Preferably, the cerium is supplied as cerium hydroxy oleate propionate complex (diluted with light mineral spirits to 40% cerium by weight). Preferred levels are toward the lower end of this range, e.g., less than 8 ppm.
- Among the specific iron compounds are: ferrocene, ferric and ferrous acetylacetonates, iron soaps like octoate and stearate (commercially available as Fe(III) compounds, usually), iron pentacarbonyl Fe(CO)5, iron napthenate, and iron tallate.
- Any of the platinum group metal compositions, e.g., 1,5-cyclooctadiene platinum diphenyl (platinum COD, also referred to as “COD-Pt-diphenyl”), described in U.S. Pat. No. 4,891,050 to Bowers, et al., U.S. Pat. No. 5,034,020 to Epperly, et al., and U.S. Pat. No. 5,266,093 to Peter-Hoblyn, et al., can be employed as the platinum source. Other suitable platinum group metal catalyst compositions include commercially-available or easily-synthesized platinum group metal acetylacetonates, platinum group metal dibenzylidene acetonates, and fatty acid soaps of tetramine platinum metal complexes, e.g., tetramine platinum oleate.
- The combustion of a fuel treated according to the invention can be of an emulsion with water, wherein an oil phase is emulsified with water, the water comprising from 1 to 30% water based on the weight of the distillate fuel, residual fuel, aviation kerosene or the like. In the preferred forms, the emulsion will be predominantly of the water-in-oil type and will preferably contain surfactants, lubricity additives and/or corrosion inhibitors in addition to the other components mentioned above. A discussion of suitable emulsion forms and additives is found in U.S. Pat. No. 5,743,922. The additives introduced into, the fuel in accord with the invention can improve combustion efficiency and reduce particulates without the use of oxidation catalysts or particulate filters for enhanced emissions control on diesel engines. Also, better carbon burn out in open flame combustion sources will lead to lower carbon deposits on heat transfer surfaces and lower soot oxidation temperatures on downstream heat recovery devices.
- The invention will be better understood when the above description is read in light of the following non-limiting examples, wherein all parts and percentages are given by weight, unless otherwise specifically indicated to the contrary.
- This example describes the preparation of a solid CMAC according to the invention containing a cerium catalyst composition. Two hundred grains of cerium hydroxy oleate propionate complex (diluted with light mineral spirits to 40% cerium by weight), was mixed with 40 grams of heavy mineral oil and charged into a 500 ml vacuum distillation apparatus. The flask was immersed in an oil bath with temperature control. Vacuum was applied using a water eductor mechanism and the oil bath temperature slowly increased. After about an hour, the temperature reached 125° C. and the distillation was stopped, the flask was reweighed and the resulting weight after processing indicated that 50.46 grains of solvent had distilled over to the receiver. The resulting concentrate was calculated to have a cerium metal concentration of 42% by weight. A small beaker of material produced was heated on a hot plate and the boiling point was found to be over 175° C. and suitable for processing temperatures encountered with polymers of the type employed in the invention to provide slow release fuel additive substrates.
- A solid CMAC produced in Example 1, above, is mixed to form a uniform blend with a powder of ethylene-propylene polymer (MP=150° C.) at a weight ratio of 50:50 and heated to 175° C. in i compression mold to form a slow release fuel additive insert in the form of a cylinder to be inserted in a suitable holder for placement in a fuel passage chamber.
- This example describes the preparation of a solid CMAC according to the invention containing both platinum and cerium catalyst compositions at a 50:1 weight ratio of cerium to platinum. To 200 grains of cerium hydroxy oleate propionate complex (diluted with light mineral spirits to 40% cerium) is added 3.2 grams of solid platinum acetylacetonate and the materials are ball milled overnight, to produce a semi-stable dispersion of platinum acetylacetonate in the cerium concentrate. The resulting mixture is then further mixed with 40 grams of heavy mineral oil and charged into a 500 ml vacuum distillation apparatus. The flask is immersed in an oil bath with temperature control and vacuum is applied using, a water eductor mechanism and the oil bath temperature slowly increased. Processing is completed as in Example 1.
- This example describes the preparation of a CMAC according to the invention containing both platinum and cerium catalyst compositions at a 50:1 weight ratio of cerium to platinum. In this case, 310 grains of 40% cerium concentrate was charged to a 1-liter ball mill with ceramic media. Then, 5.0 grams of platinum acetylacetonate was added to the mill and the mill sealed. The mixture was ball milled overnight, producing a semi-stable dispersion of platinum acetylacetonate in the cerium concentrate. The resultant mixture slowly (over an hour or two) deposited a small amount of solid platinum compound on the bottom of the container. A total of 288.7 grains was recovered from the ball mill and transferred to a 500 ml round bottom flask. To this, 3.0 grams oleic acid and 68 grains heavy mineral oil were added to the cerium+platinum mixture in the flask and mixed. This was vacuum distilled as in the previous examples under water eductor vacuum to an end temperature of 130° C. and allowed to cool. Analysis showed that 76.0 grams of light solvents had been removed by the distillation process leaving 283.7 grams of a viscous product containing 0.80% platinum and 40.1% cerium. The resultant final product was found to be completely soluble in hydrocarbon solvents. This product was suitable for blending with polymer powder at 175° C. to form an additive wafer that would supply fuel soluble forms of platinum and cerium in a controlled manner.
- This example repeats the procedure of Example 4, but employs added oleic acid as a dispersant in replacement for the heavy mineral oil. Processing is otherwise essentially the same.
- This example describes the preparation of another CMAC according to the invention containing cerium catalyst composition. Two hundred grams of 40% cerium concentrate was mixed with 60 grains of heavy mineral oil and charged into a 500 ml vacuum distillation apparatus. The flask was immersed in an oil bath with temperature control. Vacuum was applied using a water eductor mechanism and the oil bath temperature slowly increased. After 90 minutes, the temperature reached 160° C. and the distillation was stopped, the flask was reweighed and the resulting weight indicated that 54.84 grams of solvent had distilled over to the receiver. The resulting concentrate was calculated to have a cerium metal concentration of 39% wt. The result of this process was suitable for processing temperatures of 175° C. with high melting polymers and had a lower viscosity than Example 1, making it easier to work into a polymer powder.
- This example describes the preparation of a semisolid CMAC according to the invention containing both platinum and cerium catalyst compositions at a 50:1 weight ratio of cerium to platinum. In this procedure, platinum compound solutions in suitable solvents are added to a mixture of cerium catalyst material and solvents (as in Example 4) in the distillation apparatus. In particular, 80 grams of Platinum Plus 3100-SC, a 4.7% solution of COD-Pt-diphenyl in toluene, are added. The final processing temperatures is maintained below 100° C. to avoid the decomposition into platinum metal in the matrix.
- This example describes the preparation of a semisolid CMAC according to the invention as set out in Example 7, but employs platinum acetylacetonate in place of the COD-Pt-diphenyl, and the temperature is maintained at less than 250° C.
- The procedure of Example 7 is repeated but this time the ratio of platinum:cerium is 1:15, obtained by increasing the amount of platinum compound in the composition proportionately.
- This example describes the preparation of another CMAC according to the invention containing cerium catalyst composition. Two hundred grams of 40% cerium concentrate was mixed with 100 grains of heavy mineral oil and charged into a 500 ml vacuum distillation apparatus. The flask was immersed in an oil bath with temperature control. Vacuum was applied using a water eductor mechanism and the oil bath temperature slowly increased. After 90 minutes, the temperature reached 160° C. and the distillation was stopped, the flask was reweighed and the resulting weight indicated that about 55 grams of solvent had distilled over to the receiver. The resulting concentrate was calculated to have a cerium metal concentration of 32% wt. The result of this process was suitable for processing temperatures of 175° C. with high melting polymers and had a lower viscosity than Example 1, making it easier to work into a polymer powder.
- The above description is intended to enable the person skilled in the art to practice the invention. It is not intended to detail all of the possible modifications and variations which will become apparent to the skilled worker upon reading the description. It is intended, however, that all such modifications and variations be included within the scope of the invention which is seen in the above description and otherwise defined by the following claims. The claims are meant to cover the indicated elements and steps in any arrangement or sequence which is effective to meet the objectives intended for the invention, unless the context specifically indicates the contrary.
Claims (16)
1. A high temperature stable platinum and/or cerium fuel additive dosing unit, comprising:
(a) catalytic metal additive concentrate comprising fuel soluble platinum and/or cerium composition stable at temperatures above 100° C., uniformly dispersed in an organic carrier in relative quantities to be normally solid;
(b) encapsulated with a solid polymer as an infusion control composition.
2. A high temperature stable platinum and/or cerium fuel additive dosing unit according to claim 1 , wherein the catalytic metal additive concentrate is embedded in the polymer.
3. A high temperature stable platinum and/or cerium fuel additive dosing unit according to either of claims 1 or 2, wherein the catalytic metal additive concentrate is uniformly dispersed within the polymer.
4. A high temperature stable platinum and/or cerium fuel additive dosing unit according to any of claims 1, 2 or 3, wherein the catalytic metal additive concentrate comprises platinum acetylacetoneate.
5. A high temperature stable platinum and/or cerium fuel additive dosing unit according to any of claims 1, 2, 3 or 4, wherein the catalytic metal additive concentrate comprises a cerium soap.
6. A method of preparing a solid dosing form of fuel additive, by:
preparing a stable dispersion of platinum composition in a predetermined Pt/Ce ratio in a solution of cerium soap;
encapsulating the viscous catalytic metal additive concentrate comprising fuel soluble platinum and/or cerium composition stable at temperatures above 100° C. with a infusion controlling polymer.
7. A method according to claim 6 , wherein the viscous catalytic metal additive concentrate is encapsulated by embedding it in an infusion control polymer.
8. A method according to claim 6 , including the further steps of:
mixing the dispersion of platinum composition and cerium soap with an infusion control polymer under conditions effective to uniformly distribute the dispersion within the polymer; and
forming the resulting mixture of polymer into a dosing unit of predetermined shape.
9. A method according to claim 7 , including the further step of: embedding the dosing unit in an infusion control polymer.
10. A method of preparing a solid dosing form of fuel additive, by:
preparing a solution of a platinum and/or cerium composition including a low-boiling solvent including a sufficient amount of high-boiling solvent to retain fluidity of the composition in the absence of the low-boiling solvent;
evaporating the low-boiling solvent to prepare a viscous catalytic metal additive concentrate comprising fuel soluble platinum and/or cerium composition stable at temperatures above 100° C.;
encapsulating the viscous catalytic metal additive concentrate comprising fuel soluble platinum and/or cerium composition stable at temperatures above 100° C. with a infusion controlling polymer.
11. A method of using a solid dosing form of fuel additive, comprising:
obtaining a solid dosing form of catalyst according to any of the preceding claims; and
contacting the solid dosing form of catalyst with fuel to partially dissolve the polymer and introduce the catalyst into the fuel prior to combustion.
12. A method of forming a catalytic metal additive concentrate, comprising:
forming a mixture of a catalytic metal soap and a solvent;
removing low-boiling solvent.
13. A method according to claim 12 , wherein high boiling solvent is added prior to removing low boiling solvent.
14. A method according to claim 12 , wherein the catalytic metal soap comprises a cerium soap.
15. A method according to claim 14 , wherein the catalytic metal further comprises platinum acetylacetonate.
16. A method according to claim 14 , wherein the catalytic metal further comprises COD-Pt-diphenyl.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/394,693 US20040172876A1 (en) | 2002-03-22 | 2003-03-21 | Catalytic metal additive concentrate and method of making and using |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US36686002P | 2002-03-22 | 2002-03-22 | |
US10/394,693 US20040172876A1 (en) | 2002-03-22 | 2003-03-21 | Catalytic metal additive concentrate and method of making and using |
Publications (1)
Publication Number | Publication Date |
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US20040172876A1 true US20040172876A1 (en) | 2004-09-09 |
Family
ID=28675293
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US10/394,693 Abandoned US20040172876A1 (en) | 2002-03-22 | 2003-03-21 | Catalytic metal additive concentrate and method of making and using |
Country Status (8)
Country | Link |
---|---|
US (1) | US20040172876A1 (en) |
EP (1) | EP1487944A4 (en) |
JP (1) | JP2005520927A (en) |
CN (1) | CN1653163A (en) |
AU (1) | AU2003228344A1 (en) |
CA (1) | CA2481889A1 (en) |
MX (1) | MXPA04009221A (en) |
WO (1) | WO2003083017A1 (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070015656A1 (en) * | 2005-07-18 | 2007-01-18 | Valentine James M | Fuel Additive and Fuel Treatment Process |
US20080263940A1 (en) * | 2005-11-18 | 2008-10-30 | Parish W Wesley | Combustion Catalyst Carriers and Methods of Using the Same |
US9475004B2 (en) | 2014-06-06 | 2016-10-25 | Clean Diesel Technologies, Inc. | Rhodium-iron catalysts |
US9511353B2 (en) | 2013-03-15 | 2016-12-06 | Clean Diesel Technologies, Inc. (Cdti) | Firing (calcination) process and method related to metallic substrates coated with ZPGM catalyst |
US9511358B2 (en) | 2013-11-26 | 2016-12-06 | Clean Diesel Technologies, Inc. | Spinel compositions and applications thereof |
US9511350B2 (en) | 2013-05-10 | 2016-12-06 | Clean Diesel Technologies, Inc. (Cdti) | ZPGM Diesel Oxidation Catalysts and methods of making and using same |
US9545626B2 (en) | 2013-07-12 | 2017-01-17 | Clean Diesel Technologies, Inc. | Optimization of Zero-PGM washcoat and overcoat loadings on metallic substrate |
US9555400B2 (en) | 2013-11-26 | 2017-01-31 | Clean Diesel Technologies, Inc. | Synergized PGM catalyst systems including platinum for TWC application |
US9700841B2 (en) | 2015-03-13 | 2017-07-11 | Byd Company Limited | Synergized PGM close-coupled catalysts for TWC applications |
US9731279B2 (en) | 2014-10-30 | 2017-08-15 | Clean Diesel Technologies, Inc. | Thermal stability of copper-manganese spinel as Zero PGM catalyst for TWC application |
US9771534B2 (en) | 2013-06-06 | 2017-09-26 | Clean Diesel Technologies, Inc. (Cdti) | Diesel exhaust treatment systems and methods |
US9861964B1 (en) | 2016-12-13 | 2018-01-09 | Clean Diesel Technologies, Inc. | Enhanced catalytic activity at the stoichiometric condition of zero-PGM catalysts for TWC applications |
US9951706B2 (en) | 2015-04-21 | 2018-04-24 | Clean Diesel Technologies, Inc. | Calibration strategies to improve spinel mixed metal oxides catalytic converters |
US10265684B2 (en) | 2017-05-04 | 2019-04-23 | Cdti Advanced Materials, Inc. | Highly active and thermally stable coated gasoline particulate filters |
US10533472B2 (en) | 2016-05-12 | 2020-01-14 | Cdti Advanced Materials, Inc. | Application of synergized-PGM with ultra-low PGM loadings as close-coupled three-way catalysts for internal combustion engines |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0326932D0 (en) * | 2003-11-19 | 2003-12-24 | Johnson Matthey Plc | Encapsulation and dispersion method and capsule therefor |
MXPA06013947A (en) * | 2004-06-11 | 2007-03-15 | Honeywell Int Inc | Automotive additive composition. |
JP6298076B2 (en) | 2012-12-27 | 2018-03-20 | シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイShell Internationale Research Maatschappij Besloten Vennootshap | Composition |
BR112015015042A2 (en) | 2012-12-27 | 2017-07-11 | Shell Int Research | additive composition, premix for use in an additive composition, fuel or lubricant formulation, and use of a modified cyclodextrin of formula (i) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4857073A (en) * | 1987-08-27 | 1989-08-15 | Wynn Oil Company | Diesel fuel additive |
US4892562A (en) * | 1984-12-04 | 1990-01-09 | Fuel Tech, Inc. | Diesel fuel additives and diesel fuels containing soluble platinum group metal compounds and use in diesel engines |
US5501714A (en) * | 1988-12-28 | 1996-03-26 | Platinum Plus, Inc. | Operation of diesel engines with reduced particulate emission by utilization of platinum group metal fuel additive and pass-through catalytic oxidizer |
US6835218B1 (en) * | 2001-08-24 | 2004-12-28 | Dober Chemical Corp. | Fuel additive compositions |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3989759A (en) * | 1970-07-01 | 1976-11-02 | Atlantic Richfield Company | Hydroformylation process over catalyst having silica alumina support with separate alumina phase and noble metal and cobalt or nickel |
US4639255A (en) * | 1980-01-15 | 1987-01-27 | Phillips Petroleum Company | Solid form additives and method of forming same |
JPH01256593A (en) * | 1988-04-07 | 1989-10-13 | Nippon Mining Co Ltd | Fuel compositions and fuel additives |
FR2632966B1 (en) * | 1988-06-21 | 1990-11-16 | Bycosin Kemi Ab | IRON HYDROXIDE DISPERSIONS USEFUL AS COMBUSTION ADDITIVES |
DK0426978T3 (en) * | 1989-09-15 | 1996-07-29 | Erc Emissions Reduzierungs Con | Process for selective non-catalytic reduction of the emission of harmful substances from oil-fired boiler plants |
US6003303A (en) * | 1993-01-11 | 1999-12-21 | Clean Diesel Technologies, Inc. | Methods for reducing harmful emissions from a diesel engine |
GB9315974D0 (en) * | 1993-08-02 | 1993-09-15 | Ass Octel | Fuel additives |
DE4431409A1 (en) * | 1994-09-02 | 1996-05-15 | Svendborg Dampskibs As | Pumpable paste for the additive of liquid fuels |
JPH1092444A (en) * | 1996-09-13 | 1998-04-10 | Japan Gore Tex Inc | Solid polymer electrolyte composite for electrochemical reactor and electrochemical reactor using the same |
EP1409617A4 (en) * | 2000-05-08 | 2004-04-21 | Clean Diesel Tech Inc | Low-emissions diesel fuel |
EP1484386B1 (en) * | 2000-06-29 | 2008-11-26 | Neuftec Limited | Tablet |
-
2003
- 2003-03-21 JP JP2003580455A patent/JP2005520927A/en active Pending
- 2003-03-21 MX MXPA04009221A patent/MXPA04009221A/en not_active Application Discontinuation
- 2003-03-21 AU AU2003228344A patent/AU2003228344A1/en not_active Abandoned
- 2003-03-21 EP EP03726091A patent/EP1487944A4/en not_active Withdrawn
- 2003-03-21 CN CNA038112760A patent/CN1653163A/en active Pending
- 2003-03-21 CA CA002481889A patent/CA2481889A1/en not_active Abandoned
- 2003-03-21 WO PCT/US2003/008687 patent/WO2003083017A1/en active Application Filing
- 2003-03-21 US US10/394,693 patent/US20040172876A1/en not_active Abandoned
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4892562A (en) * | 1984-12-04 | 1990-01-09 | Fuel Tech, Inc. | Diesel fuel additives and diesel fuels containing soluble platinum group metal compounds and use in diesel engines |
US4857073A (en) * | 1987-08-27 | 1989-08-15 | Wynn Oil Company | Diesel fuel additive |
US5501714A (en) * | 1988-12-28 | 1996-03-26 | Platinum Plus, Inc. | Operation of diesel engines with reduced particulate emission by utilization of platinum group metal fuel additive and pass-through catalytic oxidizer |
US6835218B1 (en) * | 2001-08-24 | 2004-12-28 | Dober Chemical Corp. | Fuel additive compositions |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007011912A3 (en) * | 2005-07-18 | 2007-11-15 | Clean Diesel Tech Inc | Fuel additive and fuel treatment process |
US20070015656A1 (en) * | 2005-07-18 | 2007-01-18 | Valentine James M | Fuel Additive and Fuel Treatment Process |
US20080263940A1 (en) * | 2005-11-18 | 2008-10-30 | Parish W Wesley | Combustion Catalyst Carriers and Methods of Using the Same |
AU2006318235B2 (en) * | 2005-11-18 | 2011-05-12 | Ferox, Inc. | Combustion catalyst carriers and methods of using the same |
US7959693B2 (en) * | 2005-11-18 | 2011-06-14 | Ferox, LLC | Combustion catalyst carriers and methods of using the same |
US9511353B2 (en) | 2013-03-15 | 2016-12-06 | Clean Diesel Technologies, Inc. (Cdti) | Firing (calcination) process and method related to metallic substrates coated with ZPGM catalyst |
US9511350B2 (en) | 2013-05-10 | 2016-12-06 | Clean Diesel Technologies, Inc. (Cdti) | ZPGM Diesel Oxidation Catalysts and methods of making and using same |
US9771534B2 (en) | 2013-06-06 | 2017-09-26 | Clean Diesel Technologies, Inc. (Cdti) | Diesel exhaust treatment systems and methods |
US9545626B2 (en) | 2013-07-12 | 2017-01-17 | Clean Diesel Technologies, Inc. | Optimization of Zero-PGM washcoat and overcoat loadings on metallic substrate |
US9511358B2 (en) | 2013-11-26 | 2016-12-06 | Clean Diesel Technologies, Inc. | Spinel compositions and applications thereof |
US9555400B2 (en) | 2013-11-26 | 2017-01-31 | Clean Diesel Technologies, Inc. | Synergized PGM catalyst systems including platinum for TWC application |
US9475005B2 (en) | 2014-06-06 | 2016-10-25 | Clean Diesel Technologies, Inc. | Three-way catalyst systems including Fe-activated Rh and Ba-Pd material compositions |
US9579604B2 (en) | 2014-06-06 | 2017-02-28 | Clean Diesel Technologies, Inc. | Base metal activated rhodium coatings for catalysts in three-way catalyst (TWC) applications |
US9475004B2 (en) | 2014-06-06 | 2016-10-25 | Clean Diesel Technologies, Inc. | Rhodium-iron catalysts |
US9731279B2 (en) | 2014-10-30 | 2017-08-15 | Clean Diesel Technologies, Inc. | Thermal stability of copper-manganese spinel as Zero PGM catalyst for TWC application |
US9700841B2 (en) | 2015-03-13 | 2017-07-11 | Byd Company Limited | Synergized PGM close-coupled catalysts for TWC applications |
US9951706B2 (en) | 2015-04-21 | 2018-04-24 | Clean Diesel Technologies, Inc. | Calibration strategies to improve spinel mixed metal oxides catalytic converters |
US10533472B2 (en) | 2016-05-12 | 2020-01-14 | Cdti Advanced Materials, Inc. | Application of synergized-PGM with ultra-low PGM loadings as close-coupled three-way catalysts for internal combustion engines |
US9861964B1 (en) | 2016-12-13 | 2018-01-09 | Clean Diesel Technologies, Inc. | Enhanced catalytic activity at the stoichiometric condition of zero-PGM catalysts for TWC applications |
US10265684B2 (en) | 2017-05-04 | 2019-04-23 | Cdti Advanced Materials, Inc. | Highly active and thermally stable coated gasoline particulate filters |
Also Published As
Publication number | Publication date |
---|---|
AU2003228344A1 (en) | 2003-10-13 |
CA2481889A1 (en) | 2003-10-09 |
MXPA04009221A (en) | 2004-12-13 |
EP1487944A4 (en) | 2010-08-04 |
EP1487944A1 (en) | 2004-12-22 |
CN1653163A (en) | 2005-08-10 |
JP2005520927A (en) | 2005-07-14 |
WO2003083017A1 (en) | 2003-10-09 |
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