GB1069089A - Solid self-lubricating articles and a process for manufacturing them - Google Patents
Solid self-lubricating articles and a process for manufacturing themInfo
- Publication number
- GB1069089A GB1069089A GB24865A GB24865A GB1069089A GB 1069089 A GB1069089 A GB 1069089A GB 24865 A GB24865 A GB 24865A GB 24865 A GB24865 A GB 24865A GB 1069089 A GB1069089 A GB 1069089A
- Authority
- GB
- United Kingdom
- Prior art keywords
- telogen
- wax
- tetrafluoroethylene
- molecular weight
- rays
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 239000007787 solid Substances 0.000 title 1
- 230000003797 telogen phase Effects 0.000 abstract 8
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 abstract 7
- 239000003999 initiator Substances 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 abstract 4
- 150000003254 radicals Chemical class 0.000 abstract 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 abstract 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 abstract 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
- 230000005865 ionizing radiation Effects 0.000 abstract 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 abstract 2
- 230000008018 melting Effects 0.000 abstract 2
- 238000002844 melting Methods 0.000 abstract 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 abstract 2
- 235000010333 potassium nitrate Nutrition 0.000 abstract 2
- 239000004323 potassium nitrate Substances 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract 2
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 abstract 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical compound CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 abstract 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 abstract 1
- 239000004342 Benzoyl peroxide Substances 0.000 abstract 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 abstract 1
- LVRCEUVOXCJYSV-UHFFFAOYSA-N CN(C)S(=O)=O Chemical compound CN(C)S(=O)=O LVRCEUVOXCJYSV-UHFFFAOYSA-N 0.000 abstract 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical compound ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 abstract 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract 1
- 235000019400 benzoyl peroxide Nutrition 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 abstract 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 abstract 1
- LJSQFQKUNVCTIA-UHFFFAOYSA-N diethyl sulfide Chemical compound CCSCC LJSQFQKUNVCTIA-UHFFFAOYSA-N 0.000 abstract 1
- WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 abstract 1
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 abstract 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 abstract 1
- 229940093858 ethyl acetoacetate Drugs 0.000 abstract 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001282 iso-butane Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 abstract 1
- -1 polysiloxane Polymers 0.000 abstract 1
- 229920001296 polysiloxane Polymers 0.000 abstract 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 abstract 1
- 230000005855 radiation Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 229950011008 tetrachloroethylene Drugs 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 abstract 1
- 229940029284 trichlorofluoromethane Drugs 0.000 abstract 1
Classifications
-
- 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
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C33/00—Parts of bearings; Special methods for making bearings or parts thereof
- F16C33/02—Parts of sliding-contact bearings
- F16C33/04—Brasses; Bushes; Linings
- F16C33/20—Sliding surface consisting mainly of plastics
- F16C33/201—Composition of the plastic
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
A P.T.F.E. wax having a molecular weight in the range 700 to 100,000 is made by heating tetrafluoroethylene with a telogen in the presence or absence of a radical initiator. The telogen may be carbon tetrachloride, chloroform, ethylenetetrachloride, trichlorotrifluoroethane, dichlorodifluoromethane, trichlorofluoromethane, tetrachlorodichloroethane used singly or as a mixture of two or more thereof. Alternatively, the telogen may be a mixture of any of said substances and one or more aliphatic hydrocarbons and their derivatives having a carbon-hydrogen bond, e.g. isobutane, methylcyclohexane, dimethyl ether, tetrahydrofuran, ethylene dioxide, dioxane, trimethylamine, triethylamine, methanol, isopropanol, cyclohexanol, ethyl mercaptane, dimethyl disulphide, acetaldehyde, propionaldehyde, acetone, methyl ethyl ketone, cyclohexanone, ethyl acetate, ethyl aceto-acetate, isolactic acid, dimethyl sulphonamide, diethylsulphide, dimethyl formamide, dimethyl dichlorosilane and polysiloxane. The radical initiator may be benzoyl peroxide, diteriary butyl peroxide, azobisisobutylonitrile, diisopropyl peroxydicarbonate, tertiary butyl perbenzonate, in the range of 0.5 to 30% by weight. The P.T.F.E. wax may also be made by pyrolyzing high molecular weight P.T.F.E. resin at a temperature of about 350 DEG C. or more in the presence or absence of an alkaline metal salt, e.g. potassium nitrate. Alternatively, the P.T.F.E wax may be made by subjecting liquid tetrafluoroethylene to ionizing radiation in the presence of at least one of the fluoroalkanes referred to above for use as a telogen. Telomerization is thus effected at normal atmospheric temperature and e.g. normal atmospheric pressure. The said fluoroalkane may be in the proportion of 1 to 20 mols. per mol. of tetrafluoroethylene. The ionizing radiation may be a -rays, b -rays, g -rays, X-rays, electrons or neutrons at a rate of 102 to 108 r./hr. within a range of total radiation of 103 r. to 109 r. Additionally, the P.T.F.E. wax may be made by supplying to a reaction tower a solution comprising a radical initiator dissolved in a telogen in conjunction with excess tetrafluoroethylene gas at a pressure of 1 to 15 kg./cm2. A mixture comprising telomers, formed, excess and unreacted tetrafluoroethylene and excess telogen is removed from the top of the tower to isolate by condensation the formed telomers dispersed in excess telogen from unreacted tetrafluoroethylene. The telogen and radical initiator are as specified above. In a first example of preparing a P.T.F.E. wax, a mixture of P.T.F.E. resin having a molecular weight 2 x 106 and potassium nitrate is pyrolized at 450 DEG C. for 20 minutes to form P.T.F.E. wax having a molecular weight of 1800 and melting point of 270 DEG C. In a second example, P.T.F.E. wax having a molecular weight of 20,000 and a melting point of 320 DEG C. is prepared by telomerizing tetrafluoroethylene with carbon tetrachloride.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB24865A GB1069089A (en) | 1965-01-04 | 1965-01-04 | Solid self-lubricating articles and a process for manufacturing them |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB24865A GB1069089A (en) | 1965-01-04 | 1965-01-04 | Solid self-lubricating articles and a process for manufacturing them |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1069089A true GB1069089A (en) | 1967-05-17 |
Family
ID=9701043
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB24865A Expired GB1069089A (en) | 1965-01-04 | 1965-01-04 | Solid self-lubricating articles and a process for manufacturing them |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1069089A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6028136A (en) * | 1996-07-24 | 2000-02-22 | Centeiro Trading, Lda | Polymeric composition containing fluorographite ski sole, and method of making ski sole |
| US6121212A (en) * | 1998-03-03 | 2000-09-19 | Centeiro Trading Lda | Lubricant for improved gliding properties of skis and its application in skiing |
| WO2009116892A1 (en) * | 2008-03-17 | 2009-09-24 | Институт Проблем Химической Физики Российской Академии Наук (Ипхф Ран) | Alkylketone fluorotelomers, methods for the production thereof (variants) and a method for producing functional coatings based thereon |
| RU2525292C1 (en) * | 2013-02-21 | 2014-08-10 | Федеральное государственное бюджетное учреждение науки Институт проблем химической физики Российской академии наук (ИПХФ РАН) | Method of producing ultra-hydrophobic coatings against icing of large areas |
-
1965
- 1965-01-04 GB GB24865A patent/GB1069089A/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6028136A (en) * | 1996-07-24 | 2000-02-22 | Centeiro Trading, Lda | Polymeric composition containing fluorographite ski sole, and method of making ski sole |
| US6121212A (en) * | 1998-03-03 | 2000-09-19 | Centeiro Trading Lda | Lubricant for improved gliding properties of skis and its application in skiing |
| WO2009116892A1 (en) * | 2008-03-17 | 2009-09-24 | Институт Проблем Химической Физики Российской Академии Наук (Ипхф Ран) | Alkylketone fluorotelomers, methods for the production thereof (variants) and a method for producing functional coatings based thereon |
| RU2381237C2 (en) * | 2008-03-17 | 2010-02-10 | Некоммерческая организация Учреждение Институт проблем химической физики Российской академии наук (статус государственного учреждения (ИПХФ РАН)) | Alkylketone fluorotelomers, synthesis method thereof (versions) and method of making functional coatings based on said fluorotelomers |
| CN102007151B (en) * | 2008-03-17 | 2013-02-06 | 俄罗斯科学院化学物理课题研究所 | Alkylketone fluorotelomers, methods for the production thereof (variants) and a method for producing functional coatings based thereon |
| RU2525292C1 (en) * | 2013-02-21 | 2014-08-10 | Федеральное государственное бюджетное учреждение науки Институт проблем химической физики Российской академии наук (ИПХФ РАН) | Method of producing ultra-hydrophobic coatings against icing of large areas |
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