US2450149A - Block grease compositions - Google Patents
Block grease compositions Download PDFInfo
- Publication number
- US2450149A US2450149A US620399A US62039945A US2450149A US 2450149 A US2450149 A US 2450149A US 620399 A US620399 A US 620399A US 62039945 A US62039945 A US 62039945A US 2450149 A US2450149 A US 2450149A
- Authority
- US
- United States
- Prior art keywords
- per cent
- soap
- hydrogenated rosin
- grease
- block
- 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
- 239000004519 grease Substances 0.000 title description 50
- 239000000203 mixture Substances 0.000 title description 21
- 239000000344 soap Substances 0.000 description 68
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 52
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 48
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 48
- 235000014113 dietary fatty acids Nutrition 0.000 description 15
- 239000000194 fatty acid Substances 0.000 description 15
- 229930195729 fatty acid Natural products 0.000 description 15
- 150000004665 fatty acids Chemical class 0.000 description 15
- 239000002585 base Substances 0.000 description 14
- 239000002480 mineral oil Substances 0.000 description 12
- 235000010446 mineral oil Nutrition 0.000 description 12
- 239000003963 antioxidant agent Substances 0.000 description 10
- 235000006708 antioxidants Nutrition 0.000 description 10
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000003513 alkali Substances 0.000 description 6
- 230000006866 deterioration Effects 0.000 description 6
- 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 5
- 230000003078 antioxidant effect Effects 0.000 description 5
- 229940035422 diphenylamine Drugs 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 4
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 4
- 125000005266 diarylamine group Chemical group 0.000 description 4
- 235000021313 oleic acid Nutrition 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 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
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- -1 alkyl phenol class Chemical class 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- JJCFRYNCJDLXIK-UHFFFAOYSA-N cyproheptadine Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2C=CC2=CC=CC=C21 JJCFRYNCJDLXIK-UHFFFAOYSA-N 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N linoleic acid group Chemical group C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M5/00—Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/20—Rosin acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/066—Arylene diamines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
Definitions
- This invention relates to improved greases and more particularly to block greases having improved resistance to glazing and charring,
- Block greases are customarily employed where high bearing temperatures, such as are found in the open Journal bearings of paper mill dryers and the trunnion bearings of rotary kilns are encountered. Under such operating conditions, breakdown of the grease structure and oxidation of the organic components of the block grease are increased, with the result that the grease is rapidly consumed, loses its emciency as a lubricant, chars and often glazes on the bearing surface of the grease block.
- the object of the present invention is to prepare a block grease having a low consumption rate, good lubrication at working temperatures, and which is resistant to hardening. glazing, and charring.
- an improved block grease is obtainable by incorporating in a block grease composition a substantial proportion of hydrogenated rosin soap.
- the hydrogenated rosin soaps I have found, have the property of resisting decomposition at the elevated temperatures encountered in the use of block greases so that the resulting composition has a lower consumption rate and a greater resistance to glazing and charring than a corresponding block grease composition in which no hydrogenated rosin soap is used.
- my invention is applicable to substantially any block grease composition by substituting for a portion of the normal soap content of the block grease a corresponding proportion of a hydrogenated rosin soap. With higher proportions of hydrogenated rosin soap, higher resistance to heat decomposition, charring and glazing is obtained. I have obtained good results when as high as half of the total soap content of the block grease composition has been substituted b a hydrogenated rosin soap. Efl'ective resistance to glazing and charrin was obtained along with a low consumption rate. In general, good results can be obtained by incorporating as little as about per cent by weight or as high as 25 per cent by weight of hydrogenated rosin soap, based on the total grease composition.
- Rosin sometimes called colophony, is the residue obtained on distilling turpentine from hard pine resin.
- Abietic acid. CmHaoOa is the chief constituent of rosin and is obtained from the lat ter by distillation.
- Abietic acid contains two double bonds, and is a carboxyllc acid.
- Hydrogenated rosin is obtained essentially by the addition of hydrogen to the double bonds of abietic acid. The amount of hydrogen added may be suflicient to saturate the two unsaturated bonds of abietic acid, or it may be any amount to produce substantial partial hydrogenation.
- a particularly useful form 01' hydrogenated rosin for the purposes of my invention is hydrogenated to about per cent of capacity and has a melting point or about 168 F.
- the hydrogenated rosin soaps I prepare from hydrogenated rosin by reactin an alkali or alkaline earth basic compound with said hydrogenated rosin in the amounts necessary to obtain an approximately neutral product.
- a soap of hydrogenated rosin in my formula I prefer to use an alkali soap, and more particularly the sodium soap or hydrogenated rosin because of its cheapness and ready availability,
- the total soap content and by this term as used hereinafter, I mean to include the metallic soap of fatty acids plus the metallic soap of hydrogenated rosin, of my improved block grease may vary between 50 per cent and 20 per cent of the total weight of the grease ingredients.
- the fatty acid soaps used are obtained by the re action of metallic soaps or alkaline earth compounds with fatty acids. such as stearic, palmitic, oleic, and linoleic acids.
- oleic acid for a general utility block grease because of the resulting increased grease plasticity, or decrease of grease brittleness, when compared to a grease made with a hydrogenated rosin soap alone or mixed with sodium stearate soap.
- a ratio of about equal quantities by weight of fatty acid soap and hydrogenated rosin soap is adjustable to meet various types of open Journal and bearing surface conditions.
- very hot b aring surfaces conducive to excessive charring and glazing require a grease with a higher hydrogenated rosin soap content as compared to the fatty acid soap content.
- the mineral oil I use may have any viscosity between 100 and B 5.
- U. B. Bolt Universal seconds
- U. S. at 100 F. I ilnd that an oil of this viscosity produces a block grease that yields a desirable continuous grease film on the bearing surfaces at the temperatures usually encountered in open journals.
- Anti-oxidants may be added to my formula. However, good results are obtainable without their use, especially where the temperature of the bearing surfaces is not excessive. From experience I find that the hotter the bearing surfaces, the greater are the advantages of adding small amounts of anti-oxidants. While I prefer an anti-oxidant such as dlphenylamine, numerous other anti-oxidants may be used. For example, I may use ZA-dIamino-diphenylamine, although this latter anti-oxidant was not as efficient as my preferred diphenylam-ine anti-oxidant. 0n the other hand, I may use antioxidants of the alkali insoluble alkyl phenol class, such as 2,4,6-trialkyl phenol.
- any alkyl phenol containing a total of four or more carbon atoms in the two alkyl groups ortho to the phenolic group I find useful as an anti-oxidant.
- compounds or the classes of diarylamlne or alkali insoluble alkyl phenols I have found to be effective anti-oxidants in my block grease composition.
- preparing my block grease I may prepare the fatty acid soap and the hydrogenated rosin soap separately or together. If the respective soaps have been previously individually prepared, preparation of the "total soap content" becomes a simple matter of adding the required amounts of each component. The separate soaps are compounded with the aid of heat and stirring into a suitable mineral oil to produce the desired block grease.
- my preferred method of incorporating soap in my block grease I prepare the combined fatty acid and hydrogenated rosin soaps in situ. This method of soap formation being in situ is conducive to ease of handling and economy of time. as well as resulting in a smooth, non-fibrous block grease composition.
- Example A block grease of the following composition was prepared:
- the temperature was then gradually raised to approximately 450 F. in about 4 hours and held at this ternperature for about 1 hour under vacuum to complete the dehydration, and also to remove any entrained air which latter tends to make a grease porous and also tends to increase oil separation.
- the diphenylamine was lastly added to this mixture ten minutes before pouring into blocks.
- a second block grease was made exactly as in the example but in this latter case a rosin soap was used in lieu of the hydrogenated rosin soap. Comparative tests on these two grease compositions were made.
- the melting point (American Society for Testing Materials D566-42) of the rosin soap block grease was low, being only 360" F. as compared to a melting point of430 F. for the corresponding block grease wherein hydrogenated rosin soap was used.
- An improved block grease possessing antlcharring and anti-glazing P p rties and having a low consumption factor comprising an intimate anhydrous mixture of about '10 per cent mineral oil of a viscosity of about 200 B. U. S. at 100' It, about per cent sodium soap of a hydrogenated rosin of at least about 40 per cent saturation, about 15 per cent of sodium soup of oleic acid, and about 0.2 per cent diphenylamine.
- An improved block grease possessing anticharrinz and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 80 per cent of a mineral oil of about 100 S. U. B. at 100' I". to about 500 S. U. S. at 100 F. and about 50 per cent to about 20 per cent of soap base, the said base comprising approximately equal quantities of a soap of a hydrogenatedrosin of at least about 40 per cent saturation and a fatty acid soap, and a diarylamine in an amount suilicient to substantially inhibit oxidational deterioration.
- An improved block grease l charring and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 00 per cent of a mineral oil of about 100 B. U. B. at 100' l". to about 500 S. U. B. at 100 1''. and about 50 per cent to about 20 per cent of a soap base.
- the said base comprising approximately equal quantities of a soap of a hydrogenated rosin of at least about 40 per cent saturation and a fatty acid soap, and an alakli-insolublealkyl phenol in an amount sumcient to substantially inhibit oxidational deterioration.
- An improved block grease possessing anticharring and anti-glazing properties and having a low consumption iactor comprising an intimate anhydrous mixture or about per cent to about per cent of a mineral oil of about S. U. S. at 100 F. to about 500 B. U. 8. at 100 F. and about 50 per cent to about 20 per cent of a soap base, the said base comprising approximately equal quantities of a soap of a hydrogenated rosin of at least about 40 per cent saturation and a fatty acid soap, and an oxidation inhibitor selected from the class consisting of a diarylamine and an alkali-insoluble alky] phenol in an amount sumcient to substantially inhibit oxidational deterioration.
- An improved block grease possessing anticharrinz and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 80 per cent of a mineral oil of about 100 S. U. B. at 100' I". to about 500 S. U. S. at 100 F. and about 50 per cent to about 20 per cent of soap base, the said base comprising approximately equal quantities of a soap of a hydrogenatedrosin of at least about 40 per cent saturation and a fatty acid soap, and a diarylamine in an amount suilicient to substantially inhibit oxidational deterioration.
- An improved block grease l charring and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 00 per cent of a mineral oil of about 100 B. U. B. at 100' l". to about 500 S. U. B. at 100 1''. and about 50 per cent to about 20 per cent of a soap base.
- the said base comprising approximately equal quantities of a soap of a hydrogenated rosin of at least about 40 per cent saturation and a fatty acid soap, and an alakli-insolublealkyl phenol in an amount sumcient to substantially inhibit oxidational deterioration.
- An improved block grease possessing anticharring and anti-glazing properties and having a low consumption iactor comprising an intimate anhydrous mixture or about per cent to about per cent of a mineral oil of about S. U. S. at 100 F. to about 500 B. U. 8. at 100 F. and about 50 per cent to about 20 per cent of a soap base, the said base comprising approximately equal quantities of a soap of a hydrogenated rosin of at least about 40 per cent saturation and a fatty acid soap, and an oxidation inhibitor selected from the class consisting of a diarylamine and an alkali-insoluble alky] phenol in an amount sumcient to substantially inhibit oxidational deterioration.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Sept. 28, 1948 2,450,140 BLOCK GREASE comrosmons Paul R. McCarthy, Allison Park, Pl...
aslignor to Gulf Research a Development Company, Pittsburgh, Pa
a corporation of Delaware No Drawing. Application October 4, 1845, Serial No. 620.399
Claims. (Cl. 252-42J) This invention relates to improved greases and more particularly to block greases having improved resistance to glazing and charring,
Block greases are customarily employed where high bearing temperatures, such as are found in the open Journal bearings of paper mill dryers and the trunnion bearings of rotary kilns are encountered. Under such operating conditions, breakdown of the grease structure and oxidation of the organic components of the block grease are increased, with the result that the grease is rapidly consumed, loses its emciency as a lubricant, chars and often glazes on the bearing surface of the grease block.
The object of the present invention is to prepare a block grease having a low consumption rate, good lubrication at working temperatures, and which is resistant to hardening. glazing, and charring.
Other objects and advantages of the invention will be apparent during the course of the following description.
I have discovered that an improved block grease is obtainable by incorporating in a block grease composition a substantial proportion of hydrogenated rosin soap. The hydrogenated rosin soaps, I have found, have the property of resisting decomposition at the elevated temperatures encountered in the use of block greases so that the resulting composition has a lower consumption rate and a greater resistance to glazing and charring than a corresponding block grease composition in which no hydrogenated rosin soap is used.
I have found that my invention is applicable to substantially any block grease composition by substituting for a portion of the normal soap content of the block grease a corresponding proportion of a hydrogenated rosin soap. With higher proportions of hydrogenated rosin soap, higher resistance to heat decomposition, charring and glazing is obtained. I have obtained good results when as high as half of the total soap content of the block grease composition has been substituted b a hydrogenated rosin soap. Efl'ective resistance to glazing and charrin was obtained along with a low consumption rate. In general, good results can be obtained by incorporating as little as about per cent by weight or as high as 25 per cent by weight of hydrogenated rosin soap, based on the total grease composition.
Rosin, sometimes called colophony, is the residue obtained on distilling turpentine from hard pine resin. Abietic acid. CmHaoOa, is the chief constituent of rosin and is obtained from the lat ter by distillation. Abietic acid contains two double bonds, and is a carboxyllc acid. Hydrogenated rosin is obtained essentially by the addition of hydrogen to the double bonds of abietic acid. The amount of hydrogen added may be suflicient to saturate the two unsaturated bonds of abietic acid, or it may be any amount to produce substantial partial hydrogenation. I have found that hydrogenated rosin of about 40 per cent of saturation to and including fully hydrogenated rosin is satisfactory for use in my invention for purposes of making my alkali hydrogenated rosin soaps. Thus, I have found that soaps of both fully hydrogenated rosin and par. tially hydrogenated rosin are useful for the purpose of my invention and by the term "hydrogenated rosin soap as used hereinafter and in the appended claims I mean to include fully hydrogenated and partially hydrogenated rosin soaps.
I have found that a particularly useful form 01' hydrogenated rosin for the purposes of my invention is hydrogenated to about per cent of capacity and has a melting point or about 168 F.
The hydrogenated rosin soaps I prepare from hydrogenated rosin by reactin an alkali or alkaline earth basic compound with said hydrogenated rosin in the amounts necessary to obtain an approximately neutral product. In using a soap of hydrogenated rosin in my formula, I prefer to use an alkali soap, and more particularly the sodium soap or hydrogenated rosin because of its cheapness and ready availability,
The total soap content," and by this term as used hereinafter, I mean to include the metallic soap of fatty acids plus the metallic soap of hydrogenated rosin, of my improved block grease may vary between 50 per cent and 20 per cent of the total weight of the grease ingredients. The fatty acid soaps used are obtained by the re action of metallic soaps or alkaline earth compounds with fatty acids. such as stearic, palmitic, oleic, and linoleic acids. In general, I prefer to use oleic acid for a general utility block grease because of the resulting increased grease plasticity, or decrease of grease brittleness, when compared to a grease made with a hydrogenated rosin soap alone or mixed with sodium stearate soap. In a particularly advantageous form of my invention I use a ratio of about equal quantities by weight of fatty acid soap and hydrogenated rosin soap. However, this soap ratio is adjustable to meet various types of open Journal and bearing surface conditions. Thus, for example, very hot b aring surfaces conducive to excessive charring and glazing require a grease with a higher hydrogenated rosin soap content as compared to the fatty acid soap content.
The mineral oil I use may have any viscosity between 100 and B 5. U. B. (Baybolt Universal seconds) at 100 R. but in the most advantageous form of my invention I use an oil with about 200 S. U. S. at 100 F. I ilnd that an oil of this viscosity produces a block grease that yields a desirable continuous grease film on the bearing surfaces at the temperatures usually encountered in open journals.
Anti-oxidants may be added to my formula. However, good results are obtainable without their use, especially where the temperature of the bearing surfaces is not excessive. From experience I find that the hotter the bearing surfaces, the greater are the advantages of adding small amounts of anti-oxidants. While I prefer an anti-oxidant such as dlphenylamine, numerous other anti-oxidants may be used. For example, I may use ZA-dIamino-diphenylamine, although this latter anti-oxidant was not as efficient as my preferred diphenylam-ine anti-oxidant. 0n the other hand, I may use antioxidants of the alkali insoluble alkyl phenol class, such as 2,4,6-trialkyl phenol. In fact, any alkyl phenol containing a total of four or more carbon atoms in the two alkyl groups ortho to the phenolic group I find useful as an anti-oxidant. In general, compounds or the classes of diarylamlne or alkali insoluble alkyl phenols I have found to be effective anti-oxidants in my block grease composition.
In preparing my block grease, I may prepare the fatty acid soap and the hydrogenated rosin soap separately or together. If the respective soaps have been previously individually prepared, preparation of the "total soap content" becomes a simple matter of adding the required amounts of each component. The separate soaps are compounded with the aid of heat and stirring into a suitable mineral oil to produce the desired block grease. However. in my preferred method of incorporating soap in my block grease, I prepare the combined fatty acid and hydrogenated rosin soaps in situ. This method of soap formation being in situ is conducive to ease of handling and economy of time. as well as resulting in a smooth, non-fibrous block grease composition. In preparing my soap in situ I add the fatty acid. alkali solution and part of the oil to the pressure kettle and heat until the saponiiication reaction is complete, after which the contents of the pressure kettle are emptied into an open vessel. at which point the remaining oil is added. The grease is then maintained at a constant temperature well above the boiling point of water until the moisture content is substantially lowered to a desired amount, at which point the anti-oxidant. if desired in the formula. is added.
The following particular example will serve to illustrate the principle of this invention:
Example A block grease of the following composition was prepared:
Per cent by weight Petroleum oil (8. U. S. viscosity of 200 at 100 F.) 70.6 Hydrogenated rosin 12.7 Oleic acid 12.? Sodium hydroxide 3.8 Diphenylamine 0-2 In preparing this block grease, about 40 per cent of the total mineral oil, all of the hydrogenated rosin. and all of the fatty acid were added to a pressure kettle containing the caustic soda in aqueous solution of 40 per cent strength. The temperature of the kettle was raised to about 350 F. through a time interval of 1% hours. Heating with stirring was continued for about 1 hour at approximately 350 F. and lbs. per square inch pressure. The kettle contents were discharged into an open vessel where substantial dehydration was effected by heating with stirring, to approximately 270 F. with gradual addition of the remaining mineral oil. The temperature was then gradually raised to approximately 450 F. in about 4 hours and held at this ternperature for about 1 hour under vacuum to complete the dehydration, and also to remove any entrained air which latter tends to make a grease porous and also tends to increase oil separation. The diphenylamine was lastly added to this mixture ten minutes before pouring into blocks.
A second block grease was made exactly as in the example but in this latter case a rosin soap was used in lieu of the hydrogenated rosin soap. Comparative tests on these two grease compositions were made.
The melting point (American Society for Testing Materials D566-42) of the rosin soap block grease was low, being only 360" F. as compared to a melting point of430 F. for the corresponding block grease wherein hydrogenated rosin soap was used.
In a block grease consumption test run at a Journal temperature of 230 F. to 240 F. at 210 feet per minute at 1,000 grams applied pressure using 2% inches by 2% inches blocks, the amount of block grease consumed when using wood rosin soap was 132.6 grams, whereas the amount of corresponding block grease using hydrogenated rosin soap in lieu of rosin soap was only 4 grams.
Similarly, consistency-temperature data regarding the hereinabove corresponding block greases showed the following results:
Hydrogen Wood Rosin Consistency-Temperature 522 808') Block tea Tell-BB Unwcrksd (room temp). 64 76 Worked (room tem1p.) 193 20s Unworked at 72 134 Unworked at 180 F... 80 Unworked at 220 F 8B 186 Unworksd at 260 F 93 liXl These data were obtained by the method of the American Society for Testing Materials D217- 3ST.
Inasmuch as greases showing the least consistency changes over a wide temperature range are preferred in the block grease art due to the corresponding low consumption factor, it is evident that the hydrogenated rosin soap block grease is of superior merit in this respect as well, when compared to the analogous block grease formula in which wood rosin soap is used in lieu of hydrogenated rosin soap.
It is to be understood that my invention, herein described, is not to be limited to the details recited herein by way of example. and that various changes in the composition may be resorted to. without departing from the spirit of my invention or the scope of the subloined claims.
What I claim as my invention is:
1. An improved block grease possessing antlcharring and anti-glazing P p rties and having a low consumption factor comprising an intimate anhydrous mixture of about '10 per cent mineral oil of a viscosity of about 200 B. U. S. at 100' It, about per cent sodium soap of a hydrogenated rosin of at least about 40 per cent saturation, about 15 per cent of sodium soup of oleic acid, and about 0.2 per cent diphenylamine.
2.-An improved block grease possessing anticharring and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 80 per cent of a mineral oil of about 100 B. U. S. at 100' I". to about 500 S. U. S. at 100 F, and about 60 per cent to about per cent of soap base. the said base comprising approximately equal quantities of sodium hydrogenated rosin of at least about 40 per cent saturation and sodium olcate with about 0.2 per cent diphenylamine.
3. An improved block grease possessing anticharrinz and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 80 per cent of a mineral oil of about 100 S. U. B. at 100' I". to about 500 S. U. S. at 100 F. and about 50 per cent to about 20 per cent of soap base, the said base comprising approximately equal quantities of a soap of a hydrogenatedrosin of at least about 40 per cent saturation and a fatty acid soap, and a diarylamine in an amount suilicient to substantially inhibit oxidational deterioration.
4. An improved block grease l charring and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 00 per cent of a mineral oil of about 100 B. U. B. at 100' l". to about 500 S. U. B. at 100 1''. and about 50 per cent to about 20 per cent of a soap base.
6 the said base comprising approximately equal quantities of a soap of a hydrogenated rosin of at least about 40 per cent saturation and a fatty acid soap, and an alakli-insolublealkyl phenol in an amount sumcient to substantially inhibit oxidational deterioration.
5. An improved block grease possessing anticharring and anti-glazing properties and having a low consumption iactor comprising an intimate anhydrous mixture or about per cent to about per cent of a mineral oil of about S. U. S. at 100 F. to about 500 B. U. 8. at 100 F. and about 50 per cent to about 20 per cent of a soap base, the said base comprising approximately equal quantities of a soap of a hydrogenated rosin of at least about 40 per cent saturation and a fatty acid soap, and an oxidation inhibitor selected from the class consisting of a diarylamine and an alkali-insoluble alky] phenol in an amount sumcient to substantially inhibit oxidational deterioration.
PAUL R. McCAR'I'HY.
REFERENCES CITED The following references are of record in the file of this patent:
UNII'ED s'ra'rss PATENTS Number Name Date 2,399,063 Bchantz Apr. 23, 1946 FOREIGN PATENTS Number Country Date 414,812 Germany June 2, 1945 OTHER REFERENCES Dreshfleld et al.. Btaybellite-A ELvdrogenated Rosin for Size, article in Paper Trade Journal. July 17, 1941, pages 40 to 42 ('Dappi sectionmes 84to86).
Certificate of Correction It is hereby certified that September as, 1948.
PAUL R. McOARTHY errors appear in the printed specification of the above numbered patent requiring correction as follows:
Column 2, line 41, for the word soaps read alkali; column 6, line 34, list of references cited, for the date June 2, 1945 read June 2, 1925; line 37, for
bellite read Stag befits and that the said Letters Patent should be read with these corrections therein that the same may conform to the record of the case in the Patent Ofice.
Signed and sealed this 7th day of December, A. D. 1948.
THOMAS F. MURPHY,
Assistant Gonmiuioaer of Patents.
charring and anti-glazing P p rties and having a low consumption factor comprising an intimate anhydrous mixture of about '10 per cent mineral oil of a viscosity of about 200 B. U. S. at 100' It, about per cent sodium soap of a hydrogenated rosin of at least about 40 per cent saturation, about 15 per cent of sodium soup of oleic acid, and about 0.2 per cent diphenylamine.
2.-An improved block grease possessing anticharring and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 80 per cent of a mineral oil of about 100 B. U. S. at 100' I". to about 500 S. U. S. at 100 F, and about 60 per cent to about per cent of soap base. the said base comprising approximately equal quantities of sodium hydrogenated rosin of at least about 40 per cent saturation and sodium olcate with about 0.2 per cent diphenylamine.
3. An improved block grease possessing anticharrinz and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 80 per cent of a mineral oil of about 100 S. U. B. at 100' I". to about 500 S. U. S. at 100 F. and about 50 per cent to about 20 per cent of soap base, the said base comprising approximately equal quantities of a soap of a hydrogenatedrosin of at least about 40 per cent saturation and a fatty acid soap, and a diarylamine in an amount suilicient to substantially inhibit oxidational deterioration.
4. An improved block grease l charring and anti-glazing properties and having a low consumption factor comprising an intimate anhydrous mixture of about 50 per cent to about 00 per cent of a mineral oil of about 100 B. U. B. at 100' l". to about 500 S. U. B. at 100 1''. and about 50 per cent to about 20 per cent of a soap base.
6 the said base comprising approximately equal quantities of a soap of a hydrogenated rosin of at least about 40 per cent saturation and a fatty acid soap, and an alakli-insolublealkyl phenol in an amount sumcient to substantially inhibit oxidational deterioration.
5. An improved block grease possessing anticharring and anti-glazing properties and having a low consumption iactor comprising an intimate anhydrous mixture or about per cent to about per cent of a mineral oil of about S. U. S. at 100 F. to about 500 B. U. 8. at 100 F. and about 50 per cent to about 20 per cent of a soap base, the said base comprising approximately equal quantities of a soap of a hydrogenated rosin of at least about 40 per cent saturation and a fatty acid soap, and an oxidation inhibitor selected from the class consisting of a diarylamine and an alkali-insoluble alky] phenol in an amount sumcient to substantially inhibit oxidational deterioration.
PAUL R. McCAR'I'HY.
REFERENCES CITED The following references are of record in the file of this patent:
UNII'ED s'ra'rss PATENTS Number Name Date 2,399,063 Bchantz Apr. 23, 1946 FOREIGN PATENTS Number Country Date 414,812 Germany June 2, 1945 OTHER REFERENCES Dreshfleld et al.. Btaybellite-A ELvdrogenated Rosin for Size, article in Paper Trade Journal. July 17, 1941, pages 40 to 42 ('Dappi sectionmes 84to86).
Certificate of Correction It is hereby certified that September as, 1948.
PAUL R. McOARTHY errors appear in the printed specification of the above numbered patent requiring correction as follows:
Column 2, line 41, for the word soaps read alkali; column 6, line 34, list of references cited, for the date June 2, 1945 read June 2, 1925; line 37, for
bellite read Stag befits and that the said Letters Patent should be read with these corrections therein that the same may conform to the record of the case in the Patent Ofice.
Signed and sealed this 7th day of December, A. D. 1948.
THOMAS F. MURPHY,
Assistant Gonmiuioaer of Patents.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US620399A US2450149A (en) | 1945-10-04 | 1945-10-04 | Block grease compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US620399A US2450149A (en) | 1945-10-04 | 1945-10-04 | Block grease compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2450149A true US2450149A (en) | 1948-09-28 |
Family
ID=24485767
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US620399A Expired - Lifetime US2450149A (en) | 1945-10-04 | 1945-10-04 | Block grease compositions |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2450149A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2580570A (en) * | 1950-04-24 | 1952-01-01 | Gulf Research Development Co | Smooth-textured lithium-base greases |
| US2636859A (en) * | 1951-01-29 | 1953-04-28 | Sinclair Refining Co | Composition of matter |
| US2820762A (en) * | 1952-04-01 | 1958-01-21 | Exxon Research Engineering Co | Mixed hydroxy fatty acid-unsaturated fatty acid thickened grease compositions |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE414612C (en) * | 1922-05-24 | 1925-06-02 | Hugo Stinnes Riebeck Montan Un | Process for the production of lubricants |
| US2399063A (en) * | 1944-03-23 | 1946-04-23 | Hercules Powder Co Ltd | Lubricating grease |
-
1945
- 1945-10-04 US US620399A patent/US2450149A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE414612C (en) * | 1922-05-24 | 1925-06-02 | Hugo Stinnes Riebeck Montan Un | Process for the production of lubricants |
| US2399063A (en) * | 1944-03-23 | 1946-04-23 | Hercules Powder Co Ltd | Lubricating grease |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2580570A (en) * | 1950-04-24 | 1952-01-01 | Gulf Research Development Co | Smooth-textured lithium-base greases |
| US2636859A (en) * | 1951-01-29 | 1953-04-28 | Sinclair Refining Co | Composition of matter |
| US2820762A (en) * | 1952-04-01 | 1958-01-21 | Exxon Research Engineering Co | Mixed hydroxy fatty acid-unsaturated fatty acid thickened grease compositions |
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