US2819681A - Treatment of metal surfaces to increase the coefficient of friction - Google Patents
Treatment of metal surfaces to increase the coefficient of friction Download PDFInfo
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- US2819681A US2819681A US544614A US54461455A US2819681A US 2819681 A US2819681 A US 2819681A US 544614 A US544614 A US 544614A US 54461455 A US54461455 A US 54461455A US 2819681 A US2819681 A US 2819681A
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- silica
- dried
- rail
- friction
- colloidal
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- 229910052751 metal Inorganic materials 0.000 title description 18
- 239000002184 metal Substances 0.000 title description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 68
- 239000000377 silicon dioxide Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 16
- 239000000843 powder Substances 0.000 claims description 9
- 229910000831 Steel Inorganic materials 0.000 description 14
- 239000010959 steel Substances 0.000 description 14
- 238000012360 testing method Methods 0.000 description 14
- 230000003137 locomotive effect Effects 0.000 description 11
- 239000003921 oil Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 150000004760 silicates Chemical class 0.000 description 9
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 230000001965 increasing effect Effects 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000008119 colloidal silica Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000004964 aerogel Substances 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000005049 silicon tetrachloride Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000003405 preventing effect Effects 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 241000219289 Silene Species 0.000 description 1
- 241001125929 Trisopterus luscus Species 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000005261 decarburization Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000012254 powdered material Substances 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B61—RAILWAYS
- B61C—LOCOMOTIVES; MOTOR RAILCARS
- B61C15/00—Maintaining or augmenting the starting or braking power by auxiliary devices and measures; Preventing wheel slippage; Controlling distribution of tractive effort between driving wheels
- B61C15/08—Preventing wheel slippage
- B61C15/085—Preventing wheel slippage by dispersion of a fluid, e.g. containing chemicals
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16D—COUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
- F16D69/00—Friction linings; Attachment thereof; Selection of coacting friction substances or surfaces
- F16D69/02—Composition of linings ; Methods of manufacturing
- F16D69/027—Compositions based on metals or inorganic oxides
Definitions
- This invention relates to a new and improved adhesion treatment of metal surfaces and more particularly to a method and composition for increasing the coefficient of friction between metal surfaces capable of motion one with respect to the other.
- the invention is especially concerned with the provision of chemical means for pre venting wheel slippage between locomotive wheels and rails.
- the invention contemplates the improvement of frictional contact between metal surfaces which are susceptible of slippage one with respect to the other, as, for example, the slippage which occurs between a shaft and a sheave, gear or pinion frictionally mounted on said shaft.
- rail slip is said to result from a tough invisible oil film on the wear band of the rail. Traffic and heat destroy this film and high adhesion results.
- a water film forms across the wear band where it may contact oil deposits on the edge of a rail with the result that a film of oil creeps through and replaces the water film.
- the oil deposits on the rail sides act as reservoirs for the formation of new oil films and water acts as the transporting agent.
- the oil deposits on the rail come from journal box oil leakage by way of the outside face and outer portion of the tread of the car wheels. There are other sources of contamination such as road crossings, rail lubricators, and the like.
- Another object of this invention is to provide a method for raising the coeflicient of friction between railway car wheels and rails.
- Still another object is to raise the coefficient of friction between railway car wheels and rails having an oil film thereon.
- a further object is to provide a method of decreasing slippage between railway wheels and rails.
- Another object is to provide a chemical treatment to prevent locomotive slippage on dry, wet, or oily rails.
- Still a further object is to enable railroad locomotives to utilize more of their tractive forces on wet oily rails than has heretofore been considered possible.
- An additional object of the invention is to produce a railway rail containing an adherent coating of a material which substantially prevents slippage between the rail and a locomotive or railway car Wheel.
- Still a further object is to provide a method of substantially preventing slippage between the bearing surfaces of a railway rail and a locomotive or a railway car wheel by applying to the rail and/ or wheel a solid of colloidal fineness which acts on a slip inhibiting substance.
- A. further and more specific object of the invention is to provide a new and improved method for improving the frictional contact between a metal shaft and a sheave, gear or pinion frictionally mounted thereon.
- the coefficient of friction between metal surfaces capable of motion one with respect to the other can be increased by applying to at least one of the contacting surfaces a dried silica of colloidal fineness.
- the inventoin in its preferred embodiment is particularly applicable to increasing the coeiiicient of friction between railway car wheels and tracks by applying to at least one of the contacting surfaces thereof a dried silica of colloidal fineness.
- the preferred type of dried silica employed in accordance with the invention is one when added to a liquid such as water or ethyl alcohol will form a silica sol.
- the silica employed for the purpose of the invention is available commercially and includes dried silica sols (e. g., a silica sol containing 30% Si0 in water which has been dried but is still hydrated), fine silicas made by burning silicon tetrachloride, dried surface esterified silicas (e. g., du Pout Valron), and the so-called silica aerogols (e. g., Santocel C and Santocel 54).
- the colloidal silicates can also be employed in accordance with the invention but are less desirable, particularly if the ratio of Na O to SiO- is greater than 1:32.
- colloidal silicas, both crystalline and amorphous, and the colloidal silicates, both crystalline and amorphous have been described by Iler, The Colloid Chemistry of Silica and Silicates, Cornell Press, 1955, and the present invention contemplates the use of any and all of such colloidal silicas and colloidal silicates, with the further proviso, however, that the colloidal silicas are preferred for the practice of the invention.
- colloidal silicas and silicates whether amorphous or crystalline, have a specific surface areav greater than about 20 square meters per gram.
- the expressions dried colloidal silica and dried colloidal silicates are sometimes employed herein to describe colloidal silicas and silicates, respectively, in the form of finely divided solid particles.
- estersils The surface esterfied silicas which are employed for the purpose of the present invention are sometimes called estersils and form a new class of hydrophobic gels and powders as disclosed, for example, in Iler, U. S. 2,657,149.
- estersils are characterized by the chemical attachment of a monomolecular layer of primary or secondary alkoxy groups containing 2 to 18 carbon atoms to the silica surface. They can be produced by heating the silica with alcoholrin the absence of any substantial amount of free water at a temperature of 190 C. for one hour in the case of the primary alcohols, or at a temperature up to 275 C. in the case of the secondary alcohols.
- the structure of the silica is unchanged by the esterification of the surface but the product is organophilic and where the coating is substantially complete, the product is hydrophobic.
- Aerogels Certain fine silicas fall in the class known as aerogels.
- An aerogel is a gel in which the liquid phase has been replaced by a gaseous phase in such a way as to avoid the shrinkage which would have occurred if the gel had been dried directly from a liquid.
- the method of manufacture on a commercial scale has been described by White, Chem. Indus. 51, 66-69 (1942); Trans. Am. Inst. Chem. Engrs. 38, 435-446 (1942). While the present invention contemplates the employment of the aerogels,
- the ratio of SiO to Na O in the composition is at least 3.2: 1.
- the specific surface area can vary within a relatively wide range, for example, within the range of 20 to 800 square meters per gram.
- the ultimate particle size can also vary within a relatively wide range, for example, within the range of 8 to 1000 millimicrons in diameter.
- the silica or silicate particles can be either hydrophilic or hydrophobic.
- a steel rail was used as the base surface upon which the test was run.
- a U-shaped member made of heavy strap steel was formed having two perpendicular pieces attached to the tips of the U.
- a W diameter hole was bored in the center of the base of the U.
- a 1%" diameter steel ball having a Brinell hardness of 500 was welded to a threaded steel rod.
- the threaded steel rod was placed in, the hole formed in the U-shaped steel member and fastened with a nut so that the steel ball was within the cradle of the U.
- the perpendicular arms were fitted with small steel boxes capable of holding lead shot or other weighted material.
- the U-shaped member was placedon the rail so the steel ball rested on the surface of thevrail.
- wires were attachedat a point slightly above the rail surface.
- Fixed to the other-ends of'the wire was a short piece of string that passed over a fixed pulley, the top of which was approximately coplanar'with the surface of the rail.
- At theopposite end of the string was a suspended container which could be filled with weights.
- the boxes were filled with lead shot in an amount which, when included with the weight of the cradle, and fixtures, exerted a pressure at point of contact on the rail of 73,900 pounds per square inch.
- the weight of the U-shaped member and ball was 3,065 grams, which, for the purposes of experiment, may be considered as the operative downward pressure.
- the suspended container was filled gradually with lead shot until the steel ball just started to slide. This amount of weightisconsidered as the force necessary to overcome the-friction existing between the balland the rail. Using these two factors, the coeflicient of friction may readily be evolved from the following simple equation:
- the Hi Sil 233 had a greater tendency to form a silica sol than the Hi Sil X303 and the latter was not much better than the blank. It will also be noted that the aerogels, namely, the Santocel products, were less effective than the dried silica sols or the dried estersil.
- the fine silica either in the form of SiO as such or mixed with a minor proportion of N820 or other oxides, such as CaO, can be applied to the metal surface as a powder but this is sometimes difficult under conditions where the surface is being subjected to motion either by movement of the surface or by movement of air or other medium, around the surface.
- one preferred method of application is to mold the fine silica into a solid stick by the use of a binder, such as dextrin, a plastic or a resin, and then apply the stick to the metal surface. can be prepared in this manner.
- the particle size of the preferred dried colloidal silicas is preferably one micron or less but the aggregate form may be larger due to the drying methods employed.
- fine silica as used herein is intended to include the dried silica sols, dried silica gels, fine silicas derived by dehydrating silicic acid, silicas derived by burning silicon tetrachloride, and also the dried colloidal alkali metal silicates.
- the dried colloidal silicates as previously pointed out are generally less effective than the dried colloidal silica sols. Their effectiveness can be increased when they are used in conjunction with other substances containing finely divided discrete particles, such as fine clay (kaolin) and other finely divided water insoluble materials (e. g., oxides and/or carbonates). These same materials can also be mixed with the dried colloidal sols.
- the invention is believed to be especially important in improving the frictional contact between wheels and rails, it is contemplated that it can be applied generally to improving the frictional contact between two metal surfaces capable of motion one with respect to the other.
- the improvement of frictional contact involves contacting parts which are normally in motion (or dynamic) during the period when optimum frictional contact is desired.
- the invention is also applicable to improving the frictional contact between a metal shaft and a sheave or between a gear and a metal shaft or Any of the dried colloidal silicas between a pinion and a metal shaft where the sheave, gear or pinion is frictionally mounted on the shaft.
- a coating of the fine silica powder is applied to the shaft and the frictionally mounted member is forced on the shaft so that the colloidal silica is between said member and the shaft.
- the invention can be applied to form a layer or coating of colloidal silica between bolts and lock nuts, and between other parts which are normally desired to remain static.
- the method of improving the frictional contact between two metal surfaces capable of motion one with respect to the other which comprises applying to at least one of said surfaces a fine silica in powder form having a specific surface area of at least 20 square meters per gram, and bringing said surfaces into contact with one another with said fine silica therebetween.
- a structure having two metal surfaces capable of motion one with respect to the other and adapted to engage each other by frictional contact, at. least one of said surfaces being coated with a thin coating of fine silica in powder form having a specific surface area of at least 20 square meters per gram.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
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- Inorganic Chemistry (AREA)
- Lubricants (AREA)
Description
1958 G. w. LUVISI 2,819,681
TREATMENT OF AL s FACES TO INCREASE INVENTOR."
GEORGE W. LUVlSI AT 'Ys TREATMENT OF METAL SURFACES TO INCREASE THE COEFFICIENT OF FRICTION George W. Luvisi, Chicago, 11]., assignor to National Alnrninate Corporation, Chicago, 111., a corporation of Delaware Application November 2, 1955, Serial No. 544,614
7 Claims. (Cl. 104-1) This invention relates to a new and improved adhesion treatment of metal surfaces and more particularly to a method and composition for increasing the coefficient of friction between metal surfaces capable of motion one with respect to the other. The invention is especially concerned with the provision of chemical means for pre venting wheel slippage between locomotive wheels and rails. However, in its broader aspects the invention contemplates the improvement of frictional contact between metal surfaces which are susceptible of slippage one with respect to the other, as, for example, the slippage which occurs between a shaft and a sheave, gear or pinion frictionally mounted on said shaft.
The past several decades have produced railway locomotives possessing great power and weight, thus enabling long, heavily-laden trains to be pulled by single engines. With the advent of the extremely heavy locomotive it was felt that driving wheel slip would be eliminated. It was soon discovered, however, that the increased static weight carried on the driving wheels did not solve the problem to any great extent. Track sanding techniques were developed but this only partially alleviated the condition. Wheel slippage has proven to be an erratic condition which has not in all cases been satisfactorily explained.
In one explanation of the problem, rail slip is said to result from a tough invisible oil film on the wear band of the rail. Traffic and heat destroy this film and high adhesion results. When a light rain occurs or when the rails reach the dew point, as the result of the relatively high humidity, a water film forms across the wear band where it may contact oil deposits on the edge of a rail with the result that a film of oil creeps through and replaces the water film. The oil deposits on the rail sides act as reservoirs for the formation of new oil films and water acts as the transporting agent. The oil deposits on the rail come from journal box oil leakage by way of the outside face and outer portion of the tread of the car wheels. There are other sources of contamination such as road crossings, rail lubricators, and the like.
The importance of solving the problem is strikingly illustrated when it is realized that only 15% of the engines weight can be utilized as tractive force when the rails are greasy and moist, and when the rails are clean, dry and sanded. Even a small improvement in these figures, as expressed in the terms of increased coefiicient of friction, would enable railway locomotives to operate more efficiently and economically as well as providing improved braking for railway locomotives and rolling stock.
Another instance where it is desirable to improve the frictional contact between two metal surfaces capable of motion onewith respect to the other is where a gear or pinion is frictionally mounted on a shaft. Obviously, if slippage occurs between the gear or pinion and the shaft the efiiciency of the particular operation in question is reduced or the device may even become inoperable.
It is therefore an object of this invention to provide a new, and improved, method. for enhancing the frictional 2,8 1 9,681 Patented Jan. 14, 1958 contact between two metal surfaces capable of motion one with respect to the other.
Another object of this invention is to provide a method for raising the coeflicient of friction between railway car wheels and rails.
Still another object is to raise the coefficient of friction between railway car wheels and rails having an oil film thereon.
A further object is to provide a method of decreasing slippage between railway wheels and rails.
Another object is to provide a chemical treatment to prevent locomotive slippage on dry, wet, or oily rails.
Still a further object is to enable railroad locomotives to utilize more of their tractive forces on wet oily rails than has heretofore been considered possible.
An additional object of the invention is to produce a railway rail containing an adherent coating of a material which substantially prevents slippage between the rail and a locomotive or railway car Wheel.
Still a further object is to provide a method of substantially preventing slippage between the bearing surfaces of a railway rail and a locomotive or a railway car wheel by applying to the rail and/ or wheel a solid of colloidal fineness which acts on a slip inhibiting substance.
A. further and more specific object of the invention is to provide a new and improved method for improving the frictional contact between a metal shaft and a sheave, gear or pinion frictionally mounted thereon. Other objects will appear hereinafter.
In accordance with the invention it has been found that the coefficient of friction between metal surfaces capable of motion one with respect to the other can be increased by applying to at least one of the contacting surfaces a dried silica of colloidal fineness. The inventoin in its preferred embodiment is particularly applicable to increasing the coeiiicient of friction between railway car wheels and tracks by applying to at least one of the contacting surfaces thereof a dried silica of colloidal fineness.
The preferred type of dried silica employed in accordance with the invention is one when added to a liquid such as water or ethyl alcohol will form a silica sol.
The silica employed for the purpose of the invention is available commercially and includes dried silica sols (e. g., a silica sol containing 30% Si0 in water which has been dried but is still hydrated), fine silicas made by burning silicon tetrachloride, dried surface esterified silicas (e. g., du Pout Valron), and the so-called silica aerogols (e. g., Santocel C and Santocel 54). The colloidal silicates can also be employed in accordance with the invention but are less desirable, particularly if the ratio of Na O to SiO- is greater than 1:32. The colloidal silicas, both crystalline and amorphous, and the colloidal silicates, both crystalline and amorphous, have been described by Iler, The Colloid Chemistry of Silica and Silicates, Cornell Press, 1955, and the present invention contemplates the use of any and all of such colloidal silicas and colloidal silicates, with the further proviso, however, that the colloidal silicas are preferred for the practice of the invention. In general, for the purpose of the invention the colloidal silicas and silicates, whether amorphous or crystalline, have a specific surface areav greater than about 20 square meters per gram. The expressions dried colloidal silica and dried colloidal silicates are sometimes employed herein to describe colloidal silicas and silicates, respectively, in the form of finely divided solid particles.
The surface esterfied silicas which are employed for the purpose of the present invention are sometimes called estersils and form a new class of hydrophobic gels and powders as disclosed, for example, in Iler, U. S. 2,657,149. These estersils are characterized by the chemical attachment of a monomolecular layer of primary or secondary alkoxy groups containing 2 to 18 carbon atoms to the silica surface. They can be produced by heating the silica with alcoholrin the absence of any substantial amount of free water at a temperature of 190 C. for one hour in the case of the primary alcohols, or at a temperature up to 275 C. in the case of the secondary alcohols. As reported by ller, the structure of the silica is unchanged by the esterification of the surface but the product is organophilic and where the coating is substantially complete, the product is hydrophobic.
Certain fine silicas fall in the class known as aerogels. An aerogel is a gel in which the liquid phase has been replaced by a gaseous phase in such a way as to avoid the shrinkage which would have occurred if the gel had been dried directly from a liquid. The method of manufacture on a commercial scale has been described by White, Chem. Indus. 51, 66-69 (1942); Trans. Am. Inst. Chem. Engrs. 38, 435-446 (1942). While the present invention contemplates the employment of the aerogels,
the results. obtained in practice indicate that these are less effective than the colloidal silicas derived by drying a silica sol or by burning silicon tetrachloride and also less effective than the estersils.
In practicing the invention it has been noted that where the fine powder employed contains Na O in substantial amounts, there is a tendency toward the formation of a film when the powdered material is wet with water which is less effective for the purpose of the invention than a dry coating of the same material. It is therefore preferable in the practice of the invention that the ratio of SiO to Na O in the composition to be at least 3.2: 1. In general, the specific surface area can vary within a relatively wide range, for example, within the range of 20 to 800 square meters per gram. The ultimate particle size can also vary within a relatively wide range, for example, within the range of 8 to 1000 millimicrons in diameter. The silica or silicate particles can be either hydrophilic or hydrophobic.
To illustrate the eifectiveness of the various colloidal silica and silicate powders as agents for improving the coefiicient of friction, the following test apparatus was employed:
A steel rail was used as the base surface upon which the test was run. A U-shaped member made of heavy strap steel was formed having two perpendicular pieces attached to the tips of the U. A W diameter hole was bored in the center of the base of the U. A 1%" diameter steel ball having a Brinell hardness of 500 was welded to a threaded steel rod. The threaded steel rod was placed in, the hole formed in the U-shaped steel member and fastened with a nut so that the steel ball was within the cradle of the U. The perpendicular arms were fitted with small steel boxes capable of holding lead shot or other weighted material. The U-shaped member was placedon the rail so the steel ball rested on the surface of thevrail. To either side of the inverted U, wires were attachedat a point slightly above the rail surface. Fixed to the other-ends of'the wire was a short piece of string that passed over a fixed pulley, the top of which was approximately coplanar'with the surface of the rail. At theopposite end of the string was a suspended container which could be filled with weights.
In operation, the boxes were filled with lead shot in an amount which, when included with the weight of the cradle, and fixtures, exerted a pressure at point of contact on the rail of 73,900 pounds per square inch. The weight of the U-shaped member and ball was 3,065 grams, which, for the purposes of experiment, may be considered as the operative downward pressure. The suspended container was filled gradually with lead shot until the steel ball just started to slide. This amount of weightisconsidered as the force necessary to overcome the-friction existing between the balland the rail. Using these two factors, the coeflicient of friction may readily be evolved from the following simple equation:
Coefficient of fricti0n= where P equals 3,065 grams. and F is the weight necessary to move the 3,065 grams.
During the course of testing various materials, it was necessary to make several modifications of the test apparatus. After using the rail for numerous experiments it was ground flat to remove surface abrasion and to facilitate cleaning operations. This was later substituted by a 4-inch long piece of polished heat treated steel which was rigidly held in a small wooden frame. The steel piece was 1" wide and /4" thick. It had a tensile strength of 164,200 pounds per square inch, a yield point of 159,200 pounds per square inch, a percent elongation of 17.3% and a decarburization to a depthof 0.008". An analysis of this steel showed it to contain the following:
Percent by weight In using each of these surfaces the blank tests did not vary within experimental error and hence the test method was concluded to be standardized throughout.
At the start of each series of tests the rail and ball were cleaned with scouring powder, rinsed with distilled water and dried with cellulose tissues. Periodic inspections were made of the contacting surfaces and when scratches occurred the ball and rail were polished with emery paper to renew the surface finish.
To simplify the experimental results the forces necessary to overcome the friction of the steel ball on the rail were recorded in grams. Three types of blank tests were run, the first being conducted with clean dry surfaces. The average of 10 such tests showed a force of 1835 grams necessary to move the ball. When a visible film of journal box oil was applied to the rail the average was 620 grams. When water was applied to the oil film the average was found to be 720 grams.
In the test, the results of which are shown in the following table, all of the fine silicas and silicates were applied in dry form to a test rail containing a visible. fihn of journal boX oil and the test was conducted as previously described.
Table I Average force. Test Number of in grams to No. Composition test runs cause slippage 1. Blank 10 620, 2. 30% silica sol dried 6 2,200 3. Estersil (Du Pont Valron) 15 1,700 4. Dow Corning fine silica 8 1,418 5. Santocel 54 4 987. 6. Santocel C 5 840 7. Dry sodium silicate having an Na O to SiQ ratio of. 1:3.2 4 1,075, 8. Hi Sil 233 5 920v 9. Hi Sil X303 4 637 10. Silene 2 700 In the foregoing test results it will be observed that the dried sodium silicate was much less effective than the dried silica sol or the estersil or the Dow Corning of manufacture or their particle size, some of these products had a much greater tendency to form a silica sol than others. Thus, the Hi Sil 233 had a greater tendency to form a silica sol than the Hi Sil X303 and the latter was not much better than the blank. It will also be noted that the aerogels, namely, the Santocel products, were less effective than the dried silica sols or the dried estersil.
The fine silica, either in the form of SiO as such or mixed with a minor proportion of N820 or other oxides, such as CaO, can be applied to the metal surface as a powder but this is sometimes difficult under conditions where the surface is being subjected to motion either by movement of the surface or by movement of air or other medium, around the surface. Accordingly, one preferred method of application is to mold the fine silica into a solid stick by the use of a binder, such as dextrin, a plastic or a resin, and then apply the stick to the metal surface. can be prepared in this manner. The particle size of the preferred dried colloidal silicas is preferably one micron or less but the aggregate form may be larger due to the drying methods employed.
The term fine silica as used herein is intended to include the dried silica sols, dried silica gels, fine silicas derived by dehydrating silicic acid, silicas derived by burning silicon tetrachloride, and also the dried colloidal alkali metal silicates. The dried colloidal silicates as previously pointed out are generally less effective than the dried colloidal silica sols. Their effectiveness can be increased when they are used in conjunction with other substances containing finely divided discrete particles, such as fine clay (kaolin) and other finely divided water insoluble materials (e. g., oxides and/or carbonates). These same materials can also be mixed with the dried colloidal sols.
While the invention is believed to be especially important in improving the frictional contact between wheels and rails, it is contemplated that it can be applied generally to improving the frictional contact between two metal surfaces capable of motion one with respect to the other. In the case of locomotive wheels and rails, the improvement of frictional contact involves contacting parts which are normally in motion (or dynamic) during the period when optimum frictional contact is desired. However, the invention is also applicable to improving the frictional contact between a metal shaft and a sheave or between a gear and a metal shaft or Any of the dried colloidal silicas between a pinion and a metal shaft where the sheave, gear or pinion is frictionally mounted on the shaft. In this case, a coating of the fine silica powder is applied to the shaft and the frictionally mounted member is forced on the shaft so that the colloidal silica is between said member and the shaft. Similarly, the invention can be applied to form a layer or coating of colloidal silica between bolts and lock nuts, and between other parts which are normally desired to remain static.
The present application is a continuation-impart of my application Serial No. 533,190 filed September 8, 1955, now Patent No. 2,787,968 which in turn is a continuation-in-part of my application Serial No. 484,171 filed January 26, 1955, and the disclosures of said applications are incorporated herein as fully as if they had been set forth in their entireties.
The invention is hereby claimed as follows:
1. The method of improving the frictional contact between two metal surfaces capable of motion one with respect to the other which comprises applying to at least one of said surfaces a fine silica in powder form having a specific surface area of at least 20 square meters per gram, and bringing said surfaces into contact with one another with said fine silica therebetween.
2. The method as claimed in claim 1 in which the fine silica is a dried silica sol.
3. A method as claimed in claim 1 in which the fine silica is a dried estersil.
4. A method as claimed in claim 1 in which the fine silica also contains Na O in a ratio of SiO to Na O less than 3.2: l.
5. A method as claimed in claim 1 in which the fine silica also contains CaO.
6. A method as claimed in claim 1 in which the metal surfaces capable of motion one with respect to the other are respectively a locomotive wheel and rail.
7. A structure having two metal surfaces capable of motion one with respect to the other and adapted to engage each other by frictional contact, at. least one of said surfaces being coated with a thin coating of fine silica in powder form having a specific surface area of at least 20 square meters per gram.
References Cited in the file of this patent UNITED STATES PATENTS 1,666,167 Connolly Apr. 17, 1923 2,408,656 Kirk Oct. 1, 1946 2,657,149 Iler Oct. 27, 1953
Claims (1)
1. THE METHOD OF IMPROVING THE FRICTIONAL CONTACT BETWEEN TWO METAL SURFACES CAPABLE OF MOTION ONE WITH RESPECT TO THE OTHER WHICH COMPRISES APPLYING TO AT LEAST ONE OF SAID SURFACE A FINE SILICIA IN POWDER FORM HAVING A SPECIFIC SURFACE AREA OF AT LEAST 20 SQUARE METERS PER GRAM, AND BRINGING SAID SURFACES INTO CONTACT WITH ONE ANOTHER WITH SAID FINE SILICA THEREBETWEEN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US544614A US2819681A (en) | 1955-11-02 | 1955-11-02 | Treatment of metal surfaces to increase the coefficient of friction |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US544614A US2819681A (en) | 1955-11-02 | 1955-11-02 | Treatment of metal surfaces to increase the coefficient of friction |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2819681A true US2819681A (en) | 1958-01-14 |
Family
ID=24172895
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US544614A Expired - Lifetime US2819681A (en) | 1955-11-02 | 1955-11-02 | Treatment of metal surfaces to increase the coefficient of friction |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2819681A (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3035988A (en) * | 1958-03-19 | 1962-05-22 | Dover Chemical Corp | Method of forming friction film on hand |
| US3120818A (en) * | 1955-01-26 | 1964-02-11 | Nalco Chemical Co | Treating metal surfaces to increase the coefficient of friction |
| US3170969A (en) * | 1960-08-01 | 1965-02-23 | Bernard J Lerner | Gas-liquid contacting operations |
| US3421913A (en) * | 1964-11-12 | 1969-01-14 | Air Reduction | Method of stabilizing friction coefficient of carbonaceous base materials and the products thereof |
| US3621179A (en) * | 1970-02-16 | 1971-11-16 | Tetronics Res & Dev Co Ltd | Cleaning metal surfaces to remove grease films |
| US3850691A (en) * | 1973-04-26 | 1974-11-26 | Gen Motors Corp | Process for cleaning railway rail and improving the traction |
| US5123357A (en) * | 1989-09-01 | 1992-06-23 | Daifuki Co., Ltd. | Conveyor driven by linear motor with rolling surface of rail acting as secondary for the motor |
| US5456744A (en) * | 1993-02-23 | 1995-10-10 | Fattor; Arthur P. | Traction with diatomaceous earth |
| US6352294B1 (en) * | 1996-12-17 | 2002-03-05 | Tomoe Electric Manufacturing Co., Ltd. | Wheel for a track travel moving body, moving body provided with same, rail and travelling equipment using rail |
| US20030134935A1 (en) * | 2002-01-16 | 2003-07-17 | Schirmer David C. | Traction enhancement composition |
| US20030167717A1 (en) * | 1999-12-13 | 2003-09-11 | Faus Group, Inc. | Embossed-in-registration flooring system |
| US10286460B2 (en) | 2017-04-07 | 2019-05-14 | Robert J. Murphy | Single-pass, single-radial layer, circumferential-progression fill-welding system, apparatus and method for refurbishing railway and other transit rails |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1666167A (en) * | 1927-09-27 | 1928-04-17 | Connolly John Laurence | Railway rail, wheel, and brake shoe |
| US2408656A (en) * | 1943-04-27 | 1946-10-01 | Du Pont | Process for producing silicic acid sols |
| US2657149A (en) * | 1952-10-21 | 1953-10-27 | Du Pont | Method of esterifying the surface of a silica substrate having a reactive silanol surface and product thereof |
-
1955
- 1955-11-02 US US544614A patent/US2819681A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1666167A (en) * | 1927-09-27 | 1928-04-17 | Connolly John Laurence | Railway rail, wheel, and brake shoe |
| US2408656A (en) * | 1943-04-27 | 1946-10-01 | Du Pont | Process for producing silicic acid sols |
| US2657149A (en) * | 1952-10-21 | 1953-10-27 | Du Pont | Method of esterifying the surface of a silica substrate having a reactive silanol surface and product thereof |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3120818A (en) * | 1955-01-26 | 1964-02-11 | Nalco Chemical Co | Treating metal surfaces to increase the coefficient of friction |
| US3035988A (en) * | 1958-03-19 | 1962-05-22 | Dover Chemical Corp | Method of forming friction film on hand |
| US3170969A (en) * | 1960-08-01 | 1965-02-23 | Bernard J Lerner | Gas-liquid contacting operations |
| US3421913A (en) * | 1964-11-12 | 1969-01-14 | Air Reduction | Method of stabilizing friction coefficient of carbonaceous base materials and the products thereof |
| US3621179A (en) * | 1970-02-16 | 1971-11-16 | Tetronics Res & Dev Co Ltd | Cleaning metal surfaces to remove grease films |
| US3850691A (en) * | 1973-04-26 | 1974-11-26 | Gen Motors Corp | Process for cleaning railway rail and improving the traction |
| US5123357A (en) * | 1989-09-01 | 1992-06-23 | Daifuki Co., Ltd. | Conveyor driven by linear motor with rolling surface of rail acting as secondary for the motor |
| US5456744A (en) * | 1993-02-23 | 1995-10-10 | Fattor; Arthur P. | Traction with diatomaceous earth |
| US6352294B1 (en) * | 1996-12-17 | 2002-03-05 | Tomoe Electric Manufacturing Co., Ltd. | Wheel for a track travel moving body, moving body provided with same, rail and travelling equipment using rail |
| US20030167717A1 (en) * | 1999-12-13 | 2003-09-11 | Faus Group, Inc. | Embossed-in-registration flooring system |
| US20030134935A1 (en) * | 2002-01-16 | 2003-07-17 | Schirmer David C. | Traction enhancement composition |
| US10286460B2 (en) | 2017-04-07 | 2019-05-14 | Robert J. Murphy | Single-pass, single-radial layer, circumferential-progression fill-welding system, apparatus and method for refurbishing railway and other transit rails |
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