Patent · US4529826A · A · US
Solid lubricant and process for preparing it
- (11) Publication number
- US4529826A
- (21) Application number
- US-63394484-A
- (22) Filing date
- 1984-07-24
- (30) Priority date
- 1983-07-28
- (43) Publication date
- 1985-07-16
- (45) Date of grant
- 1985-07-16
- (52) CPC
- C09G Polishing compositions; ski waxes: 3/00
- C10M Lubricating compositions; use of chemical substances either alone or as lubricating ingredients in a lubricating composition: 101/02, 105/50, 105/52, 111/00, 131/04, 169/04, 2205/163, 2211/022, 2211/06, 2211/063
- C10N Indexing scheme associated with subclass C10M relating to lubricating compositions: 2030/06, 2030/26, 2050/08
- (73) Assignee
- ENICHIMICA SECONDARIA
- (54) Title
- Solid lubricant and process for preparing it
- (57) Abstract
A solid lubricant, consisting of solid perfluorocarbons, with linear or substantially linear carbon atoms chain, containing from 10 to 20 carbon atoms and having a value of surface tension ranging from 13 to 15 dyne/cm, is obtained by dimerization or co-dimerization of perfluorocarbonsulphonyl halogenides C.sub.n F.sub.2n+1 SO.sub.2 X (in which X represents an atom of halogen), having a linear or substantially linear chain of carbon atoms and bearing the --SO 2 X group at one end of the chain, operating at high temperature, with short reaction times, and preferably in the presence of a metal catalyst. The solid perfluorocarbon lubricant can be used, if desired as a mixture with paraffinic wax, on sliding surfaces, particularly consisting of a polymeric material either porous or made porous.
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Claims (5)
- Process for preparing a solid lubricant, consisting of solid perfluorocarbons, with a linear or substantially linear chain of carbon atoms, containing from 10 to 20 carbon atoms and having values of the crytical surface tension ranging from 13 to 15 dyne/cm, characterized in that perfluorocarbonsulphonyl halides C n F 2n+1 --SO 2 X, in which X is a halogen and n is an even or lower than 10 number, with linear or substantially linear chain and bearing the --SO 2 X group at one end of the chain are submitted to a reaction of dimerization or of co-dimerization, operating at a temperature between 400° and 550° C. and for a time of from 1 to 30 seconds.
- Process as claimed in claim 1, characterized in that X in the formula C n F 2n+1 --SO 2 X represents fluorine.
- Process as claimed in claim 1, characterized in that n in the formula C n F 2n+1 --SO 2 X ranges from 4 to 8.
- Process as claimed in claim 1, characterized in that the reaction is effected in the presence of a catalytic metal chosen among copper, nickel and chromium.
- Process as claimed in the claims 1 or 4, characterized in that the perfluorocarbonsulphonyl halides are fed in as vapours at one end of a tubular reaction vessel containing copper, nickel or chromium in the form either of powder or of pellets, as a fixed bed.
Citations (1)
- US3129254A
Record as JSON
{
"publication_number": "US4529826A",
"country": "US",
"kind": "A",
"title": "Solid lubricant and process for preparing it",
"abstract": "A solid lubricant, consisting of solid perfluorocarbons, with linear or substantially linear carbon atoms chain, containing from 10 to 20 carbon atoms and having a value of surface tension ranging from 13 to 15 dyne/cm, is obtained by dimerization or co-dimerization of perfluorocarbonsulphonyl halogenides C.sub.n F.sub.2n+1 SO.sub.2 X (in which X represents an atom of halogen), having a linear or substantially linear chain of carbon atoms and bearing the --SO 2 X group at one end of the chain, operating at high temperature, with short reaction times, and preferably in the presence of a metal catalyst. The solid perfluorocarbon lubricant can be used, if desired as a mixture with paraffinic wax, on sliding surfaces, particularly consisting of a polymeric material either porous or made porous.",
"claims": [
"1. Process for preparing a solid lubricant, consisting of solid perfluorocarbons, with a linear or substantially linear chain of carbon atoms, containing from 10 to 20 carbon atoms and having values of the crytical surface tension ranging from 13 to 15 dyne/cm, characterized in that perfluorocarbonsulphonyl halides C n F 2n+1 --SO 2 X, in which X is a halogen and n is an even or lower than 10 number, with linear or substantially linear chain and bearing the --SO 2 X group at one end of the chain are submitted to a reaction of dimerization or of co-dimerization, operating at a temperature between 400° and 550° C. and for a time of from 1 to 30 seconds.",
"2. Process as claimed in claim 1, characterized in that X in the formula C n F 2n+1 --SO 2 X represents fluorine.",
"3. Process as claimed in claim 1, characterized in that n in the formula C n F 2n+1 --SO 2 X ranges from 4 to 8.",
"4. Process as claimed in claim 1, characterized in that the reaction is effected in the presence of a catalytic metal chosen among copper, nickel and chromium.",
"5. Process as claimed in the claims 1 or 4, characterized in that the perfluorocarbonsulphonyl halides are fed in as vapours at one end of a tubular reaction vessel containing copper, nickel or chromium in the form either of powder or of pellets, as a fixed bed."
],
"cpc": [
"C09G 3/00",
"C10M 101/02",
"C10M 105/50",
"C10M 105/52",
"C10M 111/00",
"C10M 131/04",
"C10M 169/04",
"C10M 2205/163",
"C10M 2211/022",
"C10M 2211/06",
"C10M 2211/063",
"C10N 2030/06",
"C10N 2030/26",
"C10N 2050/08"
],
"assignees": [
"ENICHIMICA SECONDARIA"
],
"filing_date": "1984-07-24",
"publication_date": "1985-07-16",
"grant_date": "1985-07-16",
"priority_date": "1983-07-28",
"application_number": "US-63394484-A",
"family_id": "26328153",
"citations": [
"US3129254A"
]
}
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