US2553183A - Fuel oil composition - Google Patents
Fuel oil composition Download PDFInfo
- Publication number
- US2553183A US2553183A US37085A US3708548A US2553183A US 2553183 A US2553183 A US 2553183A US 37085 A US37085 A US 37085A US 3708548 A US3708548 A US 3708548A US 2553183 A US2553183 A US 2553183A
- Authority
- US
- United States
- Prior art keywords
- clogging
- fuel
- fuel oil
- hydrocarbon
- glyoxalidine
- 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.)
- Expired - Lifetime
Links
- 239000000295 fuel oil Substances 0.000 title claims description 40
- 239000000203 mixture Substances 0.000 title description 22
- -1 1-AMINOETHYL2-HEPTADECENYL Chemical class 0.000 claims description 14
- 229930195733 hydrocarbon Natural products 0.000 description 26
- 150000002430 hydrocarbons Chemical class 0.000 description 26
- 239000004215 Carbon black (E152) Substances 0.000 description 24
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 23
- 239000000446 fuel Substances 0.000 description 19
- 239000003921 oil Substances 0.000 description 16
- 235000019198 oils Nutrition 0.000 description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- 239000012141 concentrate Substances 0.000 description 14
- 150000003839 salts Chemical class 0.000 description 13
- 239000002253 acid Substances 0.000 description 11
- 239000003599 detergent Substances 0.000 description 10
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 9
- 239000003208 petroleum Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000002274 desiccant Substances 0.000 description 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 229910052788 barium Inorganic materials 0.000 description 4
- 239000010771 distillate fuel oil Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000010802 sludge Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- AQZGPSLYZOOYQP-UHFFFAOYSA-N Diisoamyl ether Chemical compound CC(C)CCOCCC(C)C AQZGPSLYZOOYQP-UHFFFAOYSA-N 0.000 description 2
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000004103 aminoalkyl group Chemical group 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 159000000009 barium salts Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000002939 deleterious effect Effects 0.000 description 2
- AQEFLFZSWDEAIP-UHFFFAOYSA-N di-tert-butyl ether Chemical compound CC(C)(C)OC(C)(C)C AQEFLFZSWDEAIP-UHFFFAOYSA-N 0.000 description 2
- 239000002283 diesel fuel Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- OQCFWECOQNPQCG-UHFFFAOYSA-N 1,3,4,8-tetrahydropyrimido[4,5-c]oxazin-7-one Chemical compound C1CONC2=C1C=NC(=O)N2 OQCFWECOQNPQCG-UHFFFAOYSA-N 0.000 description 1
- LLAPDLPYIYKTGQ-UHFFFAOYSA-N 1-aminoethyl Chemical group C[CH]N LLAPDLPYIYKTGQ-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- NVJUHMXYKCUMQA-UHFFFAOYSA-N 1-ethoxypropane Chemical compound CCCOCC NVJUHMXYKCUMQA-UHFFFAOYSA-N 0.000 description 1
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical group CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- YEYKMVJDLWJFOA-UHFFFAOYSA-N 2-propoxyethanol Chemical compound CCCOCCO YEYKMVJDLWJFOA-UHFFFAOYSA-N 0.000 description 1
- ZAXCZCOUDLENMH-UHFFFAOYSA-N 3,3,3-tetramine Chemical compound NCCCNCCCNCCCN ZAXCZCOUDLENMH-UHFFFAOYSA-N 0.000 description 1
- VUBOQPNQIMKEKI-UHFFFAOYSA-N 3,8-dithiatricyclo[5.1.0.02,4]oct-5-en-4-ol Chemical compound C12SC2C=CC2(O)C1S2 VUBOQPNQIMKEKI-UHFFFAOYSA-N 0.000 description 1
- MFLVUZNCOMLLQB-UHFFFAOYSA-N 4-decan-4-yloxydecane Chemical compound CCCCCCC(CCC)OC(CCC)CCCCCC MFLVUZNCOMLLQB-UHFFFAOYSA-N 0.000 description 1
- LGAQJENWWYGFSN-UHFFFAOYSA-N 4-methylpent-2-ene Chemical group CC=CC(C)C LGAQJENWWYGFSN-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 101100277337 Arabidopsis thaliana DDM1 gene Proteins 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- DMAYGYXAEYCTFO-UHFFFAOYSA-N C(CCCCCCC)C12C(C=CC=C1)(O)[Se]2.[Ca] Chemical compound C(CCCCCCC)C12C(C=CC=C1)(O)[Se]2.[Ca] DMAYGYXAEYCTFO-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000252203 Clupea harengus Species 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000010678 Paulownia tomentosa Nutrition 0.000 description 1
- 240000002834 Paulownia tomentosa Species 0.000 description 1
- 235000004347 Perilla Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 241001591024 Samea Species 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- QHNORJFCVHUPNH-UHFFFAOYSA-L To-Pro-3 Chemical compound [I-].[I-].S1C2=CC=CC=C2[N+](C)=C1C=CC=C1C2=CC=CC=C2N(CCC[N+](C)(C)C)C=C1 QHNORJFCVHUPNH-UHFFFAOYSA-L 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000006294 amino alkylene group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- ACBGULVYYCCZEG-UHFFFAOYSA-N barium;2-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound [Ba].CC(C)(C)CC(C)(C)C1=CC=CC=C1O ACBGULVYYCCZEG-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 101150113676 chr1 gene Proteins 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- JNMDPEHWZWDZES-UHFFFAOYSA-N ethoxyethane;propane-1,2-diol Chemical compound CCOCC.CC(O)CO JNMDPEHWZWDZES-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000019688 fish Nutrition 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 235000019514 herring Nutrition 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- SCZVXVGZMZRGRU-UHFFFAOYSA-N n'-ethylethane-1,2-diamine Chemical compound CCNCCN SCZVXVGZMZRGRU-UHFFFAOYSA-N 0.000 description 1
- VGIVLIHKENZQHQ-UHFFFAOYSA-N n,n,n',n'-tetramethylmethanediamine Chemical compound CN(C)CN(C)C VGIVLIHKENZQHQ-UHFFFAOYSA-N 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000001477 organic nitrogen group Chemical group 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 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
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 239000010499 rapseed oil Substances 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 125000005156 substituted alkylene group Chemical group 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 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
- 150000003568 thioethers Chemical class 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- 239000012991 xanthate Substances 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
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/232—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring
Definitions
- This invention pertains to improvement of hydrocarbon fuels, and more particularly to fuel oil compositions capable of preventing or inhibiting the sludging and/orclogging tendencies generally exhibited by hydrocarbon fuels, such as those utilized in burner systems, tanks, Diesel and combustion engines, and other industrial and domestic equipment.
- this invention relates to fuel oil compositions capable of removing preformed deleterious matter from filters, screens, and the like which deleterious matter is formed by deterioration and/or the presence of foreign bodies (e. g. water) in the fuel oils.
- hydrocarbon distillate fuel oils particularly in cracked hydrocarbon fuels.
- distillate fuel oils particularly fuel oils ob-. tained during cracking of hydrocarbons, which fuel oils have excellent performance characteristics with respect to freedom from screen clog ging, even after extensive storage under oxidiz ing, conditions and. in the presence of water.
- said tendencies of one or more surface-active glyoxalidines, and derivatives thereof may also be added to the composition.
- hydrocarbon distillate fuel oils in which,
- the active ingredient and/or ingredients of this invention are dispersed or dissolved may be treated or untreated cracked fuel oils, or mixtures of cracked fuels with straight run fuel oils, said fuel oils having components normally distilling from about 300 F. to about 700 F.
- Preferred fuels have a boiling range of from about 340 F. to about 700 F., and particularly from about 400 F. to about 675 F.
- 'hydrocarbon distillates which are utilized as bases in compositions of this invention are cracked gasoils, fuel oils, furnace oils, burner oils, Diesel fuel oils, kerosene, etc., or mixtures of .said
- ethylenediamine diethylene triamine, triethylene tetraarnine
- tetraethylene pentamine tetramethyl methylenediamine
- propylene diamine dipropylene'f triamine
- tripropylene tetramine N-ndodecyl. diethylene triamine, N-octyle ethylene diami'rie, hydroxy. ethyl-ethylene diamine, hydrhxy. isopropyl propylene diamine, hydroxy ethyldiet hylene trlamine, hydroxy ethyl. triethylenev tetramine, N-beta-hydroxyepropyl propylene di amine'and. the like.
- glyoxalidines which, are reacted with the. above poly-. aminestolform the. glyoxalidines may include: capric, nonanoicj hendecanoic, lauric, n-tridecanoic, myristic, pentadecanoic, palrnitic, magaricf'stearic, arachidic, behenic, heneicosoic, chuytinic," lignoceric, pentacosic, cerotic, monta nic-,' palmito Ieic-, oleic, gadoleic, erucic, cetoleic, myristoleic', lanop'almic, hydroxy stearic, dihydrox-y stearic, ricinoleic acids, linoleic, elaidic, linole'nic; clupanodonic.
- fatty acids. obtained. from animal, vegee table. and fish. oils. can. be used and. the. fatty acids derived. from thefollowing fixed. fatty, oils. are, particularly preferred; cocoanut. oil, palm kernaloil. rape oil," linseedoil, soya, bean oil, sunflower. oil; perilla. oil, tung. oil, whale oil, cod and. cod. liver oil, marine-animal oil, variousfishoils.
- compositions of. this invention include:
- glyoxalidine having free amino group may be reacted with acid to form salts, while those glyoxalidines having free hydroxy or other groups can be esterified, with either inorganic or organic mono or polycarboxylic acids, or reacted to form salts of soaps of allgali, allgaline earth metals, ammonium, amine or quaternary ammonium compounds.
- detergents it is preferred to add detergents to compositions of this. invention.
- the function of the detergent agents. compositions of this invention is to act as peptizers, aid; in inhibiting or preventing the. settling and adhering of impurities and sludge. to. surfaces and allow any impurities present or formed to pass through the screen or filter system.
- Detergents which may be used are alkali, alkaline earth and heavy metals and organic nitrogen base salts of various organic acids.
- the Qi Q. Port on; Q .01 detergents may. bev naphh ni ce idi .n e acids arom i an h o r s acid aliphatic acid said; acids: containing, des r d substituent grou eamine h drox de. mem nt o and Sulfur qur nd he. i e Al p enates, c oletes. er a n th cerbam te xanthates. mar be. us
- the amount of detergent salt used may vary from between about 5 and 15% and preferably is kept below Another preferred class of detergents com- 5 prises the alkali (e. g. Na, K, Li) and/or alkaline Composition
- oll-soluble petroleum sulfonates may Sodium petroleum sulfonate 10 be obtained by various processes, such as those Hydrocarbon fuel on 75 disclosed in the U. S. Patents, 2,388,677, 2,395,713, 15 2,413 713 2 413 311 2 414 773 231 397 and if Compositions of this invention are generally desired, purified by such means as those disclosed mixed in amounts of one p less With from in U. S.
- a drying agent may be positions of this invention, a minute amount of added which is compatible with the active caustic or aromatic nitrogen compounds such as gredients of this invention.
- glycol mono-alkyl ethers e. g. erties on the bottle were observed just before and the cellosolves such as ethylene glycol monoafter removal of contents.
- the time of efflur ethyl ether, ethylene glycol mono-propyl ether, of the composition was noted for each composiethylene glycol mono-tert-butyl ether, ethylene tion and the condition of the strainer observed.
- glycol mono-butyl ether, propylene glycol mono- Emlmple H ethyl ether propylene glycol monods-oamyl ether Another test, the results of which are also tabetc.
- glycol mono-tert-butyl ether ethylene ulated below, in order to determine the eifectweglycol mono-hexyl-butyl ether, propylene glycol f f f mono-isoamyl ether, etc.
- glycerine and the ness 9 compos 0 1S H.1Ven Ion or an d sludgmg and clogging properties was conducted like may be 1 f b in the following manner: About 0.05% of base The fiq a.gener.a1 o ase compositions of this invention was added to fuel composltwn of thls mventlon' oils containing entrained moisture.
- compositions of this invention may be used -to remove deposits, formedon metal surfaces such as in tubes, evaporators, heat exchangers, distillation an'dacracking equipment-and the like. They are non-corrosive and do not interfere with the functioning of the liquid .in which dispersed.
- Anon-clogging fuel oil containingentrained moisture and normally susceptibleto cause clogging containing in combination therewith from about 0.0025% toabout 0.005% of l-aminoethyl- 2-heptadecenyl glyoxalidine and about 0.0025% of alkali metal petroleum sulfonate.
- Anon-cloggingfuel oil containing 'entrained moisture and normally susceptible to cause clo ging containing in combination therewith from about0.0025% to about 0.005% of l-aminoethyl- Z-heptadecenyl glyoxalidine, and about-0.0025% of metal salt of alkyl phenol disulfide.
- An anti-cloggingconcentrate adapted to be added to -a hydrocarbon fuel oil containing cracked components, said concentrateconsisting essentiallyof a major amount .ofa liquid hydrocarbon distillate iraction and to of l-amino-ethyl-Z-heptadecenyl glyoxalidine.
- An anti-clogging concentrate adapted to be added to a hydrocarbon fuel 011 containing cracked components, said concentrate consisting-essentially of amajor amountof-a-liquid hydrocarbon distillate fraction and 10% to 20% .of l-amino-ethyl-Zeheptadecenyl glyoxalidine'and va metal salt of alkyl phenol disulfide.
- An anti-clogging concentrate adapted to be added to a hydrocarbon fuel 'oil containing cracked components, said concentrate comprising as an essential ingredient a major amount of a liquid hydrocarbon distillate fraction and 10- 20% by weight of a glyoXalidine bearing at least one higher aliphatic hydrocarbon radical and in additionthereto a radical of the group consisting of lower amino alkyl and lower hydroxy alkyl substituents and salts thereof.
- a non-clogging fuel oil containing'entrained moisture and normally susceptible to cause clogging containing in combination therewith from about 0.0025% to about 0.005% of a glyoxalidine bearing at least one higher aliphatic hydrocarbonradical and in addition thereto a radical .of the group consisting of lower amino alkyl and lower hydroxy alkyl substituents and 'salts thereof.
- a concentrate according to claim 6 containing addition thereto up to :50 by weight :of a glycol "ether .as a drying agent.
- a hon-clogging .fuel oil containing 'en trained moisture and normally susceptible to cause clogging containing in combination "therewith about 0.002% to 0.005% of :l-aminoethyl- 2-heptadecenylglyoxalidine and-about 0;0025% 'of sodium petroleum sulfonate.
- An anti-clogging concentrate adapted to be added to a hydrocarbon fuel oil containing cracked components, said concentrate consisting essentially of a ma'jor-amount of a liquid hydrocarbon distillate fraction and 10% to 20% of 1 aminoethyl-2-heptadecenyliglyoxalidine and an alkali metal petroleum sulfonate.
- An-anti-clogg'ing concentrate adapted to be added" to a hydrocarbon fuel oil containing cracked components, said concentrate'consisting essentially of a major amount of a 'liquid'hydrocarbon distillate fraction and 10% to 20% of 1 aminoethyl 2 heptadecenyl glyoxalidine and barium salt of alkyl-phenol disulfide.
- An anti-clogging concentrate adapted be .added to a hydrocarbon fuel oil contairiing cracked components, said concentrate consisting essentially of a major-amount of 1 a liquid hydro-- carbon distillate fraction and 10% to 20% of 1--aminoethyl-2-heptadecenyl glyoxalidine .and sodium petroleum isulfonate.
- a concentrate according to claim 6 con-' taining in'addition :up .to 10% by .weight of :an
- alkali metal petroleum sulfonate alkali metal petroleum sulfonate
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Description
Patented May 15, 1951 FUEL OIL COMPOSITION 'John B'. R. Caron, North Plainfield, N. J., Calmy Wies, New York, N. Y., and Everett B. Glendenning, Cranford, N. J assignors to Shell Development Company, San Francisco, Calif., a
corporation of Delaware No Drawing. Application July 3,1948, Serial No. 37,085
This invention pertains to improvement of hydrocarbon fuels, and more particularly to fuel oil compositions capable of preventing or inhibiting the sludging and/orclogging tendencies generally exhibited by hydrocarbon fuels, such as those utilized in burner systems, tanks, Diesel and combustion engines, and other industrial and domestic equipment. In addition, this invention relates to fuel oil compositions capable of removing preformed deleterious matter from filters, screens, and the like which deleterious matter is formed by deterioration and/or the presence of foreign bodies (e. g. water) in the fuel oils.
Hydrocarbons, such as distillate fuels, for example, those having a normal distillation range of from about 300 F. to about 700 F., and particularly those from about 340 F. to about 640 F., generally have a marked tendency to deteriorate under oxidizing conditions, and to form sludge; Also, the presence of impurities in such fuels, such as the presence of moisture, dispersed water, organic and/or inorganic foreign matter, and the like, causes the formation of insoluble products which tend to settle out and adhere to surfaces with which they come in contact, thereby in turn, causing clogging or plugging of filters, strainers, screens, conduit'lines, and the like, of the equipment in which they are used. This necessitates frequent'cleamng and even replac ment of parts, thereby markedly decreasing the performance eificiency of 'various equipment which utilizes such fuel oils.
The problem of screen clogging is common, particularly in domestic fuel oil systems employing distillate fuel Oils produced by distilling or cracking of petroleum, which fuels are characterized by their relativelylow-viscosity and other properties. Fuel oils of this type generally conform to the specifications setforth in Commercial Standards C. S. 12-40 for Nos. 1, 2, and 3, Fuel Oils. Petroleum. distillates within the ranges specified and which generally do not exceed 700 F., and preferablylare below 675 F., for use as Diesel fuels, are further examples of the, type of oils which under, conditions described herein have-a tendency to clog screens or filters, particularly when such fuels contain minor amounts of water dispersed therein.
Another place where screen clogging and plug-- ging of conduit. lines is encountered is in, fuel oil storage vtanks, which latter. may be connected to burner. systems. or .engines,.'etc. The stored fuel generallyrcomes in contact .withair, moisture, etc; i whichcause formation and precipita! 17 Claims; (01. 44-71) tion of sludge materials, the latter depositing on and clogging the screens or filters used for protecting the burners or engines using such fuel oils.
It is an object of this invention to inhibit sludging tendencies of hydrocarbon fuel oils. 7 It is another object to inhibit sludging and pre.-
cipitation of contaminants in hydrocarbon distillate fuel oils, particularly in cracked hydrocarbon fuels. vide distillate fuel oils, particularly fuel oils ob-. tained during cracking of hydrocarbons, which fuel oils have excellent performance characteristics with respect to freedom from screen clog ging, even after extensive storage under oxidiz ing, conditions and. in the presence of water.
dissolving in hydrocarbon fuel oils (which normally'have a tendency to cause clogging or plugging of screens or the like), a minor amount,
which amount, however, is sufficient to inhibit.
said tendencies of one or more surface-active glyoxalidines, and derivatives thereof. If desired, a minor amount of a detergent and/ or solutizer may also be added to the composition.
The hydrocarbon distillate fuel oils in which,
the active ingredient and/or ingredients of this invention are dispersed or dissolved may be treated or untreated cracked fuel oils, or mixtures of cracked fuels with straight run fuel oils, said fuel oils having components normally distilling from about 300 F. to about 700 F. Preferred fuels have a boiling range of from about 340 F. to about 700 F., and particularly from about 400 F. to about 675 F. Specifically, 'hydrocarbon distillates which are utilized as bases in compositions of this invention are cracked gasoils, fuel oils, furnace oils, burner oils, Diesel fuel oils, kerosene, etc., or mixtures of .said
cracked fuels with the corresponding or like straight run hydrocarbon fractions.
Fuel oils which have marked tendencies towards sludging and clogging of screens, filters,
etc., are primarily cracked or blends of cracked and straight run fuel oils which have the following properties: .1
It is still another object to pro- 3 Gravity, API 29-35 ASTM dist., F.:
IBP 400-500 EBP 600-700 Sulfur, percent w 0.5-1.05
Carbon residue (10, Btms.) per centw 0.1-1.4 Pour point, F -15 whereinonaR. represents hydrogen or R1 and R can'r'epresent, hydrogen or a lower alkyl group. and Rfrepreserits an alkylene group, a lower allsyl substituted alkylene group, or a radical of the structure -CHIR.;CHR1(NHCHR1CHR1)3/ where R1 also represents hydrogen or a lower allgyl. group. and J is an integer; and X represents a OHfSI-I, SeH, Tel-1,.NI-Izl group or an amino alkylene; substituent ir'nino. group. Specifically, the polyamines. which can be used are: ethylenediamine, diethylene triamine, triethylene tetraarnine; tetraethylene pentamine, tetramethyl methylenediamine, propylene diamine, dipropylene'f triamine, tripropylene tetramine, N-ndodecyl. diethylene triamine, N-octyle ethylene diami'rie, hydroxy. ethyl-ethylene diamine, hydrhxy. isopropyl propylene diamine, hydroxy ethyldiet hylene trlamine, hydroxy ethyl. triethylenev tetramine, N-beta-hydroxyepropyl propylene di amine'and. the like.
'Acids which, are reacted with the. above poly-. aminestolform the. glyoxalidines may include: capric, nonanoicj hendecanoic, lauric, n-tridecanoic, myristic, pentadecanoic, palrnitic, magaricf'stearic, arachidic, behenic, heneicosoic, chuytinic," lignoceric, pentacosic, cerotic, monta nic-,' palmito Ieic-, oleic, gadoleic, erucic, cetoleic, myristoleic', lanop'almic, hydroxy stearic, dihydrox-y stearic, ricinoleic acids, linoleic, elaidic, linole'nic; clupanodonic. acids. and the like. In. addition. fatty acids. obtained. from animal, vegee table. and fish. oils. can. be used and. the. fatty acids derived. from thefollowing fixed. fatty, oils. are, particularly preferred; cocoanut. oil, palm kernaloil. rape oil," linseedoil, soya, bean oil, sunflower. oil; perilla. oil, tung. oil, whale oil, cod and. cod. liver oil, marine-animal oil, variousfishoils.
suchas herring. oil, sardineoiland the like. In.- stead of using the free fatty acids, their salts, esters. or, amides can beused.
specific gly-oxalidines. which may be used in.
compositions of. this invention include:
l-amino ethyl ZeheptadecenyI' glyoxalidine l-amino ethylQ-heptadecyl glyoxalidine l-arriino-v ethyl 2 -undecyl glyoxalidine l-aminoisopropyl 2-h'eptadecenyl-5-methyl glyoxalidine.
l-a'm'ino isopropyl 2 -heptadecyl-5-methy1 gly The glyoxalidine having free amino group may be reacted with acid to form salts, while those glyoxalidines having free hydroxy or other groups can be esterified, with either inorganic or organic mono or polycarboxylic acids, or reacted to form salts of soaps of allgali, allgaline earth metals, ammonium, amine or quaternary ammonium compounds. If desired, and under certain conditions of use, it is preferred to add detergents to compositions of this. invention. The function of the detergent agents. compositions of this invention is to act as peptizers, aid; in inhibiting or preventing the. settling and adhering of impurities and sludge. to. surfaces and allow any impurities present or formed to pass through the screen or filter system.
Detergents which may be used are alkali, alkaline earth and heavy metals and organic nitrogen base salts of various organic acids. The Qi Q. Port on; Q .01 detergents may. bev naphh ni ce idi .n e acids arom i an h o r s acid aliphatic acid said; acids: containing, des r d substituent grou eamine h drox de. mem nt o and Sulfur qur nd he. i e Al p enates, c oletes. er a n th cerbam te xanthates. mar be. us
P rt er y pre err d. c ass: f e e nts. ar h sa ts. Q lkr z ubst t d ph nol sulfides; or. s; se eni e: n r tellm de equivalent. These. hen ic sa t may ba en esentedby theeneral: ormula whereinlyf isa metal; RrandR', represent at least one alkylradieal, attached to.the, aromatic ring.
the. total, number of carbon. atoms in all. of.
such rad-icalsv being, at, least, 5;, X is, O. and/ or S Q is S, Se or. Te and n. is aninteger of from. lto 4. To;form. the saltsofthesephenolic compounds.
" they may betreatedgwith, such. metal compounds wherein. the, symbols. are: the. sameas referred. toy in the.- previous... formulas; These-basic salts may be. formed by. reacting, theearomatic acidic com.- pounds. with; more. than the amount of' metal oxide. or.- hydroxide necessary to. form. the. normal.
salt.
Some specifimcompoundsas represented 'bythei above formulasare: barium tertiaryoctyl phenol: sulfide. and. disulfide, barium di-rtertiaryiamyl phenohsulfid; calcium. iso hexadecyl.phenorsulefide,v magnesium,tertiaryiamyliphenolj sulfide, co halt-tertiary amyllphenohsulfide, barium dodecyl.
salicylate. sulfide, sulfide oi thee barium salt of: the ethyl? esterof: pei-hydroxyi dithi'obenzoic acid;
calcium octyl phenol selenide, etc. The amount of detergent salt used may vary from between about 5 and 15% and preferably is kept below Another preferred class of detergents com- 5 prises the alkali (e. g. Na, K, Li) and/or alkaline Composition A earth metal (e. g. Ca, Sr, Ba, Mg) salts of pe- Per cent troleum sulfonic acids, preferably of high molecl-hydroxy ethyl-2-heptadecenyl glyoxalidine- 10 ular weight, derived from petroleum hydrocarbon Hydrocarbon fuel oil 90 crudes and fractions thereof which are of the 10 so-called mixed type, i. e. containing naphtheniccomposztwn B Per cent type hydrqcarbons' l-hydroxy ethyl-Z-heptadecyl glyoxalidine These oll-soluble petroleum sulfonates may Sodium petroleum sulfonate 10 be obtained by various processes, such as those Hydrocarbon fuel on 75 disclosed in the U. S. Patents, 2,388,677, 2,395,713, 15 2,413 713 2 413 311 2 414 773 231 397 and if Compositions of this invention are generally desired, purified by such means as those disclosed mixed in amounts of one p less With from in U. S. Patents, 2,236,933, 2,334,532, 2,357,3 about 250 to about 1000 gallons of fuel oil. Thus, 2 3 3 452 and 2 40 753 for example, on a percentage basis of fuel used, The metal Salts of 1 pe ifi type of Petro- 20 one pint of any one of the above compositions, for 1 lfoni acid under discussion, or the other example per 250 gallons of fuel would correspond types of detergents may be added to the to approximately the following concentration of centrate or base in amounts of fr about 5 theactive ingredients: Organic nitrogenous comto about 15%, and preferably in amounts below Pounds as described 0-0O25% detergent 0 to 0 about 0.0025%; drying agent, 0 to about 0.265%.
In Systems wherein substantial amounts of To inhibit any corrosive tendencies of fuelcommoisture are present a drying agent may be positions of this invention, a minute amount of added which is compatible with the active caustic or aromatic nitrogen compounds such as gredients of this invention. By tying up most of amlme may be added- These compounds 3F as the free moisture in this manner the amount alkaline reserves and render the fuel composltions which would normally combine with syudgek substantially non-corrosive to copper; brass, and forming materials is diminished, thus alleviating other metalsg a most aggravating clogging problem The following illustrates the effectiveness of Drying agents which are particularly Suited are compositions of this 1nvent1on as sludge inhibithe glycol-ether type such as diethylene-glycol tors and antlcloggmg agentsmono-methyl, ethyl N- and isopropyl ether, di- Examp I M ethylene glycol mono'butyl ether, methylene To a number of sample bottles each containyc01 mo y ether, 8170- also dipropylene ing approximately 50 cc. of fuel oil normally sus glycol mono'ethyl ether, dipropylene glycol ceptible to cause clogging a minute amount of mono-isopropyl ether. dipropylene glycol monoabout 0.15 cc. of water was added and also to isoamyl ether. diisoblltylene yc mOIIO-iSO- each sample bottle about 0.05% of a specific base P DY ether, y -p pylene glycol O composition as noted in the table below was also ethyl ether, y sobu ylene glycol m0 added. The bottles were shaken thoroughly and p opy et e e170- IIlStead 0f the y -fi e I then permitted to stand for about one hour. Sus- Various alcohols may be us Such a 61 8 having pension properties of water and inert particles 6 or more carbon atoms in the m l ule su h as were observed and noted after one hour. After ylene gly y e e ycol, cetylene g yc one hour of standing the bottles were shaken etc. diglycols such as dipropylene glycol, dibuty1 again and the contents poured into a very fine ene glycol, diamylene glycol, ether alcohols and strainer container. Wetting and drainage propparticularly the glycol mono-alkyl ethers, e. g. erties on the bottle were observed just before and the cellosolves such as ethylene glycol monoafter removal of contents. The time of efflur ethyl ether, ethylene glycol mono-propyl ether, of the composition was noted for each composiethylene glycol mono-tert-butyl ether, ethylene tion and the condition of the strainer observed. glycol mono-butyl ether, propylene glycol mono- Emlmple H ethyl ether propylene glycol monods-oamyl ether Another test, the results of which are also tabetc. Also glycol mono-tert-butyl ether, ethylene ulated below, in order to determine the eifectweglycol mono-hexyl-butyl ether, propylene glycol f f f mono-isoamyl ether, etc. Also glycerine and the ness 9 compos 0 1S H.1Ven Ion or an d sludgmg and clogging properties was conducted like may be 1 f b in the following manner: About 0.05% of base The fiq a.gener.a1 o ase compositions of this invention was added to fuel composltwn of thls mventlon' oils containing entrained moisture. The sam- Per cent ples were allowed to age for two days. These Surfac ct v agent y d cs a samples were then shaken and evaluated for their derivatives thereof ;4-20 anti-clogging properties, as related in the pre- 6 Drying agent e. g. glycol-ether 0-50 Hydrocarbon fuel oil Balance Specific base (concentrate) compositions may be illustrated by the following examples:
Detergent e. g. phenate, sulfonate, etc -i0-=10 ceding para raph- 0.05% or less base composition as noted in fuel oil containing en- Properties evaluated immediately after adding concentrate to fuel oil Same properties after aging of doped fuel oil Example I Example II trained moisture asserts "irocompositions .ofzthis -inventionz=may be added minor :amounts .of .a .foaming inhibitor :such as silicon liquids, .e. g. .dimethyl silicone, fiuoro .organic compounds, chloro parafifins, salts .of alkyl alkylene phosphates and the like. Compositions of this invention may be used -to remove deposits, formedon metal surfaces such as in tubes, evaporators, heat exchangers, distillation an'dacracking equipment-and the like. They are non-corrosive and do not interfere with the functioning of the liquid .in which dispersed.
It is to .be understood that while .the features of the invention have been-described and illustrated in connection with certain specific examples, this invention, however, is not to'be limited thereto or otherwise restricted, except by the prior art and the scope of the appended-claims.
We claim as our invention:
"1. Anon-clogging fuel oil containing entrained moisture-and normally susceptible 'to cause clogging containing in combination therewith from about 0.0025% to about 0.005% of l-aminoethyl- 2-heptadecenyl glyoxalidine.
'2. Anon-clogging fuel oil containingentrained moisture and normally susceptibleto cause clogging containing in combination therewith from about 0.0025% toabout 0.005% of l-aminoethyl- 2-heptadecenyl glyoxalidine and about 0.0025% of alkali metal petroleum sulfonate.
3. Anon-cloggingfuel oil containing 'entrained moisture and normally susceptible to cause clo ging containing in combination therewith from about0.0025% to about 0.005% of l-aminoethyl- Z-heptadecenyl glyoxalidine, and about-0.0025% of metal salt of alkyl phenol disulfide.
4. An anti-cloggingconcentrate adapted to be added to -a hydrocarbon fuel oil containing cracked components, said concentrateconsisting essentiallyof a major amount .ofa liquid hydrocarbon distillate iraction and to of l-amino-ethyl-Z-heptadecenyl glyoxalidine.
5. An anti-clogging concentrate adapted to be added to a hydrocarbon fuel 011 containing cracked components, said concentrate consisting-essentially of amajor amountof-a-liquid hydrocarbon distillate fraction and 10% to 20% .of l-amino-ethyl-Zeheptadecenyl glyoxalidine'and va metal salt of alkyl phenol disulfide.
6. An anti-clogging concentrate'adapted to be added to a hydrocarbon fuel 'oil containing cracked components, said concentrate comprising as an essential ingredient a major amount of a liquid hydrocarbon distillate fraction and 10- 20% by weight of a glyoXalidine bearing at least one higher aliphatic hydrocarbon radical and in additionthereto a radical of the group consisting of lower amino alkyl and lower hydroxy alkyl substituents and salts thereof.
'7. A non-clogging fuel oil containing'entrained moisture and normally susceptible to cause clogging containing in combination therewith from about 0.0025% to about 0.005% of a glyoxalidine bearing at least one higher aliphatic hydrocarbonradical and in addition thereto a radical .of the group consisting of lower amino alkyl and lower hydroxy alkyl substituents and 'salts thereof.
8 i8. .Aiconcentrate according ztoicla'im 5'6 containing )in addition up 'to 10% :by :weight :of ;a metal sal-t of an alkyl phenoldisulfide.
9. A concentrate according to claim 6 containing addition thereto up to :50 by weight :of a glycol "ether .as a drying agent.
:10. A hon-clogging .fuel oil containing 'en trained moisture and normally susceptible to cause clogging containing in combination "therewith about 0.002% to 0.005% of :l-aminoethyl- 2-heptadecenylglyoxalidine and-about 0;0025% 'of sodium petroleum sulfonate.
11.A non-clogging fuel oil :containin'g entrained moisture and normally susceptible to cause clogging containing in combination therewith about 0.002% to 0.005% of -l-amin'oe'thyl- 2--heptadecenyl glyoxalidine and about 0.0025% of barium alkyl phenol disulfide. V
12. An anti-clogging concentrate adapted to be added to a hydrocarbon fuel oil containing cracked components, said concentrate consisting essentially of a ma'jor-amount of a liquid hydrocarbon distillate fraction and 10% to 20% of 1 aminoethyl-2-heptadecenyliglyoxalidine and an alkali metal petroleum sulfonate.
13. An-anti-clogg'ing concentrate adapted to be added" to a hydrocarbon fuel oil containing cracked components, said concentrate'consisting essentially of a major amount of a 'liquid'hydrocarbon distillate fraction and 10% to 20% of 1 aminoethyl 2 heptadecenyl glyoxalidine and barium salt of alkyl-phenol disulfide.
14. An anti-clogging concentrate adapted be .added to a hydrocarbon fuel oil contairiing cracked components, said concentrate consisting essentially of a major-amount of 1 a liquid hydro-- carbon distillate fraction and 10% to 20% of 1--aminoethyl-2-heptadecenyl glyoxalidine .and sodium petroleum isulfonate.
15. A concentrate according to claim 6 con-' taining in'addition :up .to 10% by .weight of :an
alkali metal petroleum sulfonate.
.16. A non-clogging .fuel oil containing entrained .moisture and :normally susceptible it!) cause clogging containing iin combination there with from about 0.0025% to about 0.005% ofl-hydroxyethyl-Z-heptadecenyl :glyoxalidine.
.17. A non-clogging fuel -:oil containing entrained :moisture and normally susceptible itO cause clogging containing in combination there- REFERENCES CITED The following :references are of record in ithe file of this patent:
UNITED STATES PATENTS Number Name Date 2,249,626 Cooketal July'15, 1941 2,369,490 -Proell -Feb. 13,1945
Claims (1)
1. A NON-CLOGGING FUEL OIL CONTAINING ENTRAINED MOSITURE AND NORMALLY SUSCEPTIBLE TO CAUSE CLOGGING CONTAINING IN COMBINATION THEREWITH FROM ABOUT 0.0025% TO ABOUT 0.005% OF 1-AMINOETHYL2-HEPTADECENYL GLYOXALIDINE.
Priority Applications (1)
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US37085A US2553183A (en) | 1948-07-03 | 1948-07-03 | Fuel oil composition |
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US37085A US2553183A (en) | 1948-07-03 | 1948-07-03 | Fuel oil composition |
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US2553183A true US2553183A (en) | 1951-05-15 |
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Cited By (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2668100A (en) * | 1951-11-15 | 1954-02-02 | Nat Aluminate Corp | Corrosion inhibitor for liquid hydrocarbons |
US2736641A (en) * | 1952-02-01 | 1956-02-28 | Union Oil Co | Fuel oil additive |
US2739049A (en) * | 1951-10-04 | 1956-03-20 | Exxon Research Engineering Co | Gasoline type fuel composition |
DE941217C (en) * | 1952-11-01 | 1956-04-05 | Standard Oil Dev Co | Stabilized heating oil |
US2754216A (en) * | 1953-03-11 | 1956-07-10 | Universal Oil Prod Co | Metal deactivator |
US2773879A (en) * | 1952-04-02 | 1956-12-11 | Nat Aluminate Corp | Glyoxalidine salts of long chain dicarboxylic acids |
US2839373A (en) * | 1954-04-09 | 1958-06-17 | California Research Corp | Gasoline compostion |
US2839371A (en) * | 1954-04-08 | 1958-06-17 | California Research Corp | Gasoline composition |
US2839372A (en) * | 1954-04-09 | 1958-06-17 | California Research Corp | Gasoline composition |
US2888337A (en) * | 1955-09-19 | 1959-05-26 | Universal Oil Prod Co | Stabilization of hydrocarbon oil heavier than gasoline |
US2907646A (en) * | 1955-09-29 | 1959-10-06 | American Oil Co | Rust inhibitor for fuel fractions of mineral oil |
US2908624A (en) * | 1955-12-02 | 1959-10-13 | Nat Aluminate Corp | Process of inhibiting deposition of organic substances in heat exchangers and the like operating at elevated temperatures |
US2917376A (en) * | 1955-08-03 | 1959-12-15 | Petrolite Corp | Fuel oil composition |
US2970897A (en) * | 1957-12-03 | 1961-02-07 | American Cyanamid Co | Gasoline containing antioxidants |
US2986874A (en) * | 1951-11-07 | 1961-06-06 | Gen Electric | Method of operating a jet propulsion system |
US2994596A (en) * | 1956-10-24 | 1961-08-01 | Nalco Chemical Co | Hydrocarbon liquids inhibited against corrosion |
US3036902A (en) * | 1958-03-03 | 1962-05-29 | Standard Oil Co | Motor fuel composition |
US3210168A (en) * | 1962-05-22 | 1965-10-05 | Exxon Research Engineering Co | Stabilized oiled coal slurry in water |
US3231494A (en) * | 1961-08-22 | 1966-01-25 | Exxon Research Engineering Co | Rust preventive prepared from sodium nitrite and the reaction product of fatty acid and imidazoline |
US20080221002A1 (en) * | 2004-11-19 | 2008-09-11 | Imperial Chemical Industries Plc | Dispersant |
US20090054281A1 (en) * | 2004-11-19 | 2009-02-26 | Imperial Chemical Industries Plc | Lubricating Composition Comprising a Polyester Dispersant |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2249626A (en) * | 1941-03-13 | 1941-07-15 | American Cyanamid Co | Lubricating composition |
US2369490A (en) * | 1941-06-16 | 1945-02-13 | Standard Oil Co | Stabilizers for oils |
-
1948
- 1948-07-03 US US37085A patent/US2553183A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2249626A (en) * | 1941-03-13 | 1941-07-15 | American Cyanamid Co | Lubricating composition |
US2369490A (en) * | 1941-06-16 | 1945-02-13 | Standard Oil Co | Stabilizers for oils |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2739049A (en) * | 1951-10-04 | 1956-03-20 | Exxon Research Engineering Co | Gasoline type fuel composition |
US2986874A (en) * | 1951-11-07 | 1961-06-06 | Gen Electric | Method of operating a jet propulsion system |
US2668100A (en) * | 1951-11-15 | 1954-02-02 | Nat Aluminate Corp | Corrosion inhibitor for liquid hydrocarbons |
US2736641A (en) * | 1952-02-01 | 1956-02-28 | Union Oil Co | Fuel oil additive |
US2773879A (en) * | 1952-04-02 | 1956-12-11 | Nat Aluminate Corp | Glyoxalidine salts of long chain dicarboxylic acids |
DE941217C (en) * | 1952-11-01 | 1956-04-05 | Standard Oil Dev Co | Stabilized heating oil |
US2754216A (en) * | 1953-03-11 | 1956-07-10 | Universal Oil Prod Co | Metal deactivator |
US2839371A (en) * | 1954-04-08 | 1958-06-17 | California Research Corp | Gasoline composition |
US2839373A (en) * | 1954-04-09 | 1958-06-17 | California Research Corp | Gasoline compostion |
US2839372A (en) * | 1954-04-09 | 1958-06-17 | California Research Corp | Gasoline composition |
US2917376A (en) * | 1955-08-03 | 1959-12-15 | Petrolite Corp | Fuel oil composition |
US2888337A (en) * | 1955-09-19 | 1959-05-26 | Universal Oil Prod Co | Stabilization of hydrocarbon oil heavier than gasoline |
US2907646A (en) * | 1955-09-29 | 1959-10-06 | American Oil Co | Rust inhibitor for fuel fractions of mineral oil |
US2908624A (en) * | 1955-12-02 | 1959-10-13 | Nat Aluminate Corp | Process of inhibiting deposition of organic substances in heat exchangers and the like operating at elevated temperatures |
US2994596A (en) * | 1956-10-24 | 1961-08-01 | Nalco Chemical Co | Hydrocarbon liquids inhibited against corrosion |
US2970897A (en) * | 1957-12-03 | 1961-02-07 | American Cyanamid Co | Gasoline containing antioxidants |
US3036902A (en) * | 1958-03-03 | 1962-05-29 | Standard Oil Co | Motor fuel composition |
US3231494A (en) * | 1961-08-22 | 1966-01-25 | Exxon Research Engineering Co | Rust preventive prepared from sodium nitrite and the reaction product of fatty acid and imidazoline |
US3210168A (en) * | 1962-05-22 | 1965-10-05 | Exxon Research Engineering Co | Stabilized oiled coal slurry in water |
US20080221002A1 (en) * | 2004-11-19 | 2008-09-11 | Imperial Chemical Industries Plc | Dispersant |
US20090054281A1 (en) * | 2004-11-19 | 2009-02-26 | Imperial Chemical Industries Plc | Lubricating Composition Comprising a Polyester Dispersant |
US8603957B2 (en) * | 2004-11-19 | 2013-12-10 | Croda International Plc | Lubricating composition comprising a polyester dispersant |
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