US3839425A - Perfluoroalkyletheramidoalkyl betaines and sulfobetaines - Google Patents
Perfluoroalkyletheramidoalkyl betaines and sulfobetaines Download PDFInfo
- Publication number
- US3839425A US3839425A US00072803A US7280370A US3839425A US 3839425 A US3839425 A US 3839425A US 00072803 A US00072803 A US 00072803A US 7280370 A US7280370 A US 7280370A US 3839425 A US3839425 A US 3839425A
- Authority
- US
- United States
- Prior art keywords
- acid
- carbon atoms
- betaines
- group
- compounds
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
- C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C309/13—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/14—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton containing amino groups bound to the carbon skeleton
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/905—Agent composition per se for colloid system making or stabilizing, e.g. foaming, emulsifying, dispersing, or gelling
- Y10S516/909—The agent contains organic compound containing sulfoxy*
- Y10S516/91—The compound contains nitrogen, except if present solely as NH4+
- Y10S516/912—The compound contains -C[=O]NHH where substitution may be made for the hydrogen
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/905—Agent composition per se for colloid system making or stabilizing, e.g. foaming, emulsifying, dispersing, or gelling
- Y10S516/914—The agent contains organic compound containing nitrogen, except if present solely as NH4+
- Y10S516/915—The compound contains -C[=O]NHH where substitution may be made for the hydrogen
Definitions
- Perfluoroalkyletheramidoalkyl betaines betaines having the formula wherein R; is a perfluoroalkyl group of 1 to 6 carbon atoms, n is an integer of to 8, R is hydrogen or an alkyl group of 1 to 6 carbon atoms, R is an alkylene group of 1 to 12 carbon atoms, R and R are alkyl groups each containing 1 to 6 carbon atoms, R is an alkylene group of 1 to 4 carbon atoms and X is selected from a group consisting of CO and S0 are useful as surface active agents, foaming agents, foam stabilizers and aqueous film spreading agents. They are particularly useful in fire extinguishant foam formulations.
- Surface-active agents are generally characterized as anionic, cationic, or nonionic depending upon the physicochemical properties.
- Anionic surface-active agents contain anionogenic group, usually a carboxyl, sulfonic acid or sulfuric ester, which in basic solutions form anions.
- Cationic surface-active agents contain cationogenic group, usually an amine group, which in acidic solutions form cations.
- Nonionic surface-active agents on the other hand are incapable of forming ions and depend upon highly hydrophilic groupings such as those of ether or hydroxyl for their activity.
- the betaines and the sulfobetaines of this invention constitute a distinct group of ampholytic surface-active agents in that the betaines and the sulfobetaines contain cationic quaternary ammonium group and anionic carboxylate or sulfonate group within the molecule and do not depend upon ionization to form these ions. They are basic and have a positive charge at the quaternary ammonium nitrogen but at the same time they are acidic and have a negative charge at the carboxylate or the sulfonate group.
- Betaines are defined as inner quaternary ammonium salts wherein the positive charge on the quaternary ammonium nitrogen is balanced intramolecularly by an anionic carboxylate group, i.e. compounds having the groupings g ruql 02 within the molecule.
- sulfobetaines are defined as betaine compounds wherein the anionic group within the molecule is a sulfonate group, i.e. the compounds having the groupings within the molecule.
- ampholytic surface-active agents in general have not achieved commercial importance of anionic, cationic, or non-ionic surface-active agents. Greater cost of manufacture of ampholytic surface-active agents undoubtedly is one of the reasons for the lack of commercial acceptance. Absence of some unusual properties that are not possessed by the usual anionic, cationic or nonionic surface-active agents may also account for the lack of commercial success.
- Perfiuoroalkyletheramidoalkyl betaines and sulfobetaines having the formula R N (R (R )R -X wherein R, is a perfluoroalkyl group of 1 to 6 carbon atoms, 11 is an integer of O to 8,.
- R is hydrogen or an alkyl group of 1 to 6 carbon atoms
- R is an alkylene group of l to 12 carbon atoms
- R and R are alkyl groups each containing 1 to 6 carbon atoms
- R is an alkylene group of 1 to 4 carbon atoms
- X is selected from the group consisting of CO and S0 have unusual chemical properties which make them suitable not only as surface active agents and foaming agents but also as foam stabilizers and aqueous film spreading agents. The latter two properties make these compounds particularly useful in fire extinguishant foam formulations.
- the compounds of the present invention are the betaines and the sulfobetaines of the formula R O[CF(CF )CF O] CF(CF CON(R)R N (R (R )R X wherein R n, R, R R R R and X are as designated above.
- the most preferred compounds are con o cH N cH3) (cnpcn co and
- the starting materials for the preparation of the betaines and the sulfobetaines of this invention are the perfiuoroalkylether acid fluorides of the formula R,O[C F O] CF(CF )CFO.
- acid fluorides are available either by the polymerization of hexafluoropropylene oxide or by the polymerization of a mixture of hexafluoropropylene and oxygen.
- the prod uct is the formula of F(CF2)v where x and y are 1-4 and the total of x+y is 2-5.
- R may be a branched or straight-chain perfluoralkyl group of 1-6 carbon atoms.
- the acid fluorides prepared by polymerization of mixture of hexafluoropropylene and oxygen are taught by Pasetti, Sianesi and Corti in Die Makromolekulare Chemie 86 pages 308-311 (1965); Sianesi and Fontanelli in Die 'Makrornolekulare Chemie 102 pages 115-124 (1967); and French Patent 1,434,537.
- the polymerization is carried out at temperatures of about 100 C. to 25 C.
- perfluoroalkylether acid fluorides are converted to perfluoroalkylether amidoalkylamines of the formula by the reaction of the acid fluoride with a suitable diamine or by the reaction of an alkyl ester derived from the above perfluoroalkylether acid fluoride with the diamine.
- perfluoroalkyletheramide by the reaction of perfluoroalkylether acid fluoride with an amine is described by MacKenzie in U.S. Pat. 3,274,244.
- the reaction is preferably carried out in the presence of inert solvents such as diethylether, tetrahydrofuran, benzene, trichlorotrifluoroethane and the like.
- Hydrogen fluoride formed in the reaction may be removed by using the amine in excess of that required for the reaction or by using an acid scavenger such as pyridine or triethylamine.
- the perfluoroalkylether amidoalkylamines of the formula may also be prepared by first converting the perfluoroalkylether acid fluoride to the corresponding alkylperfluoroalkylether ester and preferably the methyl ester of the formula
- the esters are prepared by esterification of the corresponding acid fluoride using standard methods, for example, reaction of the acid fluoride with an alkanol such as methanol as taught by Diesslin et al. in U.S. Pat. 2,567,- 011.
- the esterification is carried out by reacting the perfluoroalkylether acid fluoride with excess methanol at -20 C., optionally in an inert solvent, in the presence of suflicient pyridine to consume the hydrogen fluoride formed.
- methanol one can also use ethanol, propanol, butanol or the like equally well.
- the alkylperfluoroalkylether esters are then reacted with diamines of the formula HN(R)R N(R )(R to form the perfluoroalkylether amidoalkylamine of the formula R O(C F O),,CF(CF )CON ('R)R N(:R (R
- a large number of diamines of the formula A special procedure is required to obtain a perfluoroalkylether amidoalkylamine wherein R is -CH
- They are readily prepared by the reaction of the perfluoroalkyletheramide of the formula with formaldehyde and hydrogen chloride to form N- chloromethylperfluoroalkyletheramide of the formula which is then converted to the tertiary amine by the reaction with a secondary amine HN(R (R).
- the betaines and the sulfobetaines of the present invention are then prepared by reacting the above described perfluoroalkyletheramidoalkylamines with salts of haloalkylcarboxylic acid or haloalkyl sulfonic acid.
- Haloalkylcarboxylic acids and haloalkylsulfonic acids from which salts, 'for example the alkali metal salts, are readily obtained are well-known and useful examples include bromoacetic acid, chloroacetic acid, 2- bromopropionic acid, 3-bromopropionic acid, 2 chloropropionic acid, 3-chloropropionic acid, 3 chlorobutyric acid, 4-chlorobutyric acid, 5 chlorovaleric acid, chloromethylsulfonic acid, 2-bromoethane sulfonic acid, 2- chloroethane sulfonic acid, l-chloroethane sulfonic acid and 3-chloropropane sulfonic acid.
- the betaines and the sulfobetaines of the present invention are particularly effective surface active agents in water, and in neutral, strongly acidic and strongly basic aqueous solutions.
- the compounds of the present invention are equally eflective in neutral, strongly acidic and strongly basic aqueous solutions. It is clear from the structural feature of the compounds of this invention that the ionic character of the molecule is maintained in neutral, acidic and basic aqueous solutions.
- the compounds of this invention are particularly useful in the formation of aqueous foams and in stabilizing such foams after they are formed.
- the ability to form foams and to stabilize such foams are valuable, for example in fire extinguishant foam formulations.
- a is ogg gi-r gd r roaiw(oznazand IB-C0N(H)(CH2)aN (CzHs)z(CHz)2C02 46.8 49.6 41 40 94a 3.. 1 B-6l%%N Ii:I))1(H2)3N(C 4Ho)2 and B-C0N(H)( 2)aN (C4H9)rCH2CO2 44.7 44.5 3.9 3.9 91.3
- the water drop immediately spreads E l 11 and covers the hydrocarbon surface with an aqueous film.
- the ability to form aqueous film in hydrocarbon surface is not a general property of surface active agents. It is not known at present, which structural portion of the compounds of the present invention is responsible for the aqueous film spreading ability but it is believed that the perfluoroalkylether chain of the molecule is involved in this unique characteristic.
- aqueous film spreading property is extremely valuable, particularly in aqueous foam fire extinguishant compositions wherein rapidly covering of burning hydrocarbon surfaces is desirable. After such a fire has been extinguished, it is desirable to maintain foam covering to prevent reignition.
- the isopropanol was considered to be completely removed when the contents of the distillation flask reached 50 C. at 5 mm. Hg pressure.
- the residue in the flask weighing 53.7 g. was the product, which was a very tacky, slightly yel- N-dimethylaminopropylamide of perfluoroalkylether acid,
- the isopropanol extract was then placed in a distillation assembly wherein isopropanol was removed by distillation at reduced pressures.
- the isopropanol was considered to be completely removed when the contents of the distillation flask reached 50 C. at 5 mm. Hg pressure.
- the residue in the flask weighing 53.1 g. was the desired product, which was a sticky yellow semi-solid, obtained in 91% yield.
- the elementary analysis showed the following: Percent fluorine, calculated 46.9, found 46.8; percent nitrogen, calculated 4.1, found 4.0 and percent sulfur, calculated 4.7, found 4.5.
- Example 12 and 13 Using the procedure of Example 11 and equimolar amounts of the starting materials listed in Table II the perfluoroalkyletheramidoalkylsulfobetaines listed in Table II were prepared.
- Table II TABLE I1 Percent Percent fluorine nitrogen Yield, Example Reactants Suliobetaiue Calc'd Found Calc'd Found percent 12 B-COH(CH:4)(CH2)3N(CH3)2 BCON(CH3)(CH2)3N (CH3)2(CHz)3SO3 I 45.2 45.4 3.9 3.9 94.2
- Example 14-19 ample.
- the aqueous film spreading test was carried out by The utility of the compounds of the present invention as surface active agents is clearly demonstrated by the data summarized in Table III below which shows measurements of surface tension of dilute aqueous solutions of carefully Placing 10 drops of the aqueous Solution of the these compounds at 5 using a DuNouy tensiometen 15 compounds on the surface of cyclohexane contained in a It is to be notedthat even at a concentration as low as diameter evaporating dlsh and recording the 0.001% Outstanding reduction in the surface tension is time Seconds) for the cyclohexane surface to be covevident. It is also to be noted that even in the presence ered by the aqueous film.
- Example 24 is comparative of 5% hydrochloric acid or 5% sodium hydroxide the using the prior art compound of Examples 19 and
- R; CF --CF -CF mula TABLE III
- Compound concentration (g./100 ml.)
- Example Compound Medium 0 0.001 0.01 0.1 1.0
- Example 20 C F O[CF(CF )CF O],,CF(CF )CON(R)
- n is an integer of 0 to 8, this example.
- the test was conducted by placing 50 ml.
- R is hydrogen or alkyl of 1 to 6 carbon atoms of a 1% aqueous solut1on of the compound in a 1000 ml. 1 alkylene of 1 to 12 carbon atoms, Erlenmeyer flask, stoppermg the flask and then shaking R218 alkyl of 1 to 6 carbon atoms, the flask vlgorously for 10 seconds.
- the volume of the R3 is alkyl of 1 to 6 carbon atoms, foam produced, the nature of the foam, and the stability R4 is alkylene of 1 to 4 Carbon atoms and of the foam were observed.
- Tests with a 1% solution of X CO 0 SO the compound of Example 1 gave a foam volume of 400 15 2 r ml. which was thick and uniform and was stable for References Cited hours.
- Example 21 UNITED STATES PATENTS 3,681,413 8/1972 Sweeney et al. 260--501.13 Using the procedure of Example 20 and the prior art 2,764,602 9/1956 Ahlbrecht 260501.13 X compound of Example 19 a 1% aqueous solution of the 3,147,065 9/1964 Kosher et al- 260-5676 M compound gave a foam volume of 800 ml. but the foam was non-uniform with very large bubbles and was un- HOWARD T. MARS, Primary Examiner stable.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1. A COMPOSITION OF MATTER HAVING THE CHEMICAL FORMULA
C3F7O(CF(CF3)CF2O)NCF(CF3)CON(R) R1N$(R2)(R3)-R4-X$
WHEREIN N IS AN INTEGER OF 0 TO 8, R IS HYDROGEN OR ALKYL OF 1 TO 6 CARBON ATOMS, R1 IS ALKYLENE OF 1 TO 12 CARBON ATOMS, R2 IS ALKYL OF 1 TO 6 CARBON ATOMS, R3 IS ALKYL OF 1 TO 6 CARBON ATOMS, R4 IS ALKYLENE OF 1 TO 4 CARBON ATOMS, AND X IS CO2 OR SO3.
C3F7O(CF(CF3)CF2O)NCF(CF3)CON(R) R1N$(R2)(R3)-R4-X$
WHEREIN N IS AN INTEGER OF 0 TO 8, R IS HYDROGEN OR ALKYL OF 1 TO 6 CARBON ATOMS, R1 IS ALKYLENE OF 1 TO 12 CARBON ATOMS, R2 IS ALKYL OF 1 TO 6 CARBON ATOMS, R3 IS ALKYL OF 1 TO 6 CARBON ATOMS, R4 IS ALKYLENE OF 1 TO 4 CARBON ATOMS, AND X IS CO2 OR SO3.
Description
United States Patent O 3,839,425 PERFLUOROALKYLETHERAMIDOALKYL BETAINES AND SULFOBETAINES Philip Lee Bartlett, Wilmington, Del., assignor to E. L du Pont de Nemours and Company, Wilmington, Del. No Drawing. Filed Sept. 16, 1970, Ser. No. 72,803 Int. Cl. C07c 101/04 U.S. Cl. 260501.12 1 Claim ABSTRACT OF THE DISCLOSURE Perfluoroalkyletheramidoalkyl betaines betaines having the formula wherein R; is a perfluoroalkyl group of 1 to 6 carbon atoms, n is an integer of to 8, R is hydrogen or an alkyl group of 1 to 6 carbon atoms, R is an alkylene group of 1 to 12 carbon atoms, R and R are alkyl groups each containing 1 to 6 carbon atoms, R is an alkylene group of 1 to 4 carbon atoms and X is selected from a group consisting of CO and S0 are useful as surface active agents, foaming agents, foam stabilizers and aqueous film spreading agents. They are particularly useful in fire extinguishant foam formulations.
and sulfo- BACKGROUND OF THE INVENTION Surface-active agents are generally characterized as anionic, cationic, or nonionic depending upon the physicochemical properties. Anionic surface-active agents contain anionogenic group, usually a carboxyl, sulfonic acid or sulfuric ester, which in basic solutions form anions. Cationic surface-active agents contain cationogenic group, usually an amine group, which in acidic solutions form cations. Nonionic surface-active agents on the other hand are incapable of forming ions and depend upon highly hydrophilic groupings such as those of ether or hydroxyl for their activity.
There exists, however, another group of surface-active agents which is characterized by having both the anionogenic and the cationogenic groups within the molecule. This type of compound as exemplified by aminoacids is amphoteric and ampholytic. In strongly basic solutions, ionization occurs mainly at the acidic group and the molecule is predominantly anionic and acidic. In strongly acidic solution ionization occurs mainly at the amine group as ammonium ion and the molecule is predominantly cationic and basic.
The betaines and the sulfobetaines of this invention constitute a distinct group of ampholytic surface-active agents in that the betaines and the sulfobetaines contain cationic quaternary ammonium group and anionic carboxylate or sulfonate group within the molecule and do not depend upon ionization to form these ions. They are basic and have a positive charge at the quaternary ammonium nitrogen but at the same time they are acidic and have a negative charge at the carboxylate or the sulfonate group.
Betaines are defined as inner quaternary ammonium salts wherein the positive charge on the quaternary ammonium nitrogen is balanced intramolecularly by an anionic carboxylate group, i.e. compounds having the groupings g ruql 02 within the molecule. sulfobetaines are defined as betaine compounds wherein the anionic group within the molecule is a sulfonate group, i.e. the compounds having the groupings within the molecule.
The ampholytic surface-active agents in general have not achieved commercial importance of anionic, cationic, or non-ionic surface-active agents. Greater cost of manufacture of ampholytic surface-active agents undoubtedly is one of the reasons for the lack of commercial acceptance. Absence of some unusual properties that are not possessed by the usual anionic, cationic or nonionic surface-active agents may also account for the lack of commercial success.
SUMMARY OF THE INVENTION Perfiuoroalkyletheramidoalkyl betaines and sulfobetaines having the formula R N (R (R )R -X wherein R, is a perfluoroalkyl group of 1 to 6 carbon atoms, 11 is an integer of O to 8,. R is hydrogen or an alkyl group of 1 to 6 carbon atoms, R is an alkylene group of l to 12 carbon atoms, R and R are alkyl groups each containing 1 to 6 carbon atoms, R is an alkylene group of 1 to 4 carbon atoms and X is selected from the group consisting of CO and S0 have unusual chemical properties which make them suitable not only as surface active agents and foaming agents but also as foam stabilizers and aqueous film spreading agents. The latter two properties make these compounds particularly useful in fire extinguishant foam formulations.
DESCRIPTION OF THE INVENTION The compounds of the present invention are the betaines and the sulfobetaines of the formula R O[CF(CF )CF O] CF(CF CON(R)R N (R (R )R X wherein R n, R, R R R R and X are as designated above.
The most preferred compounds are con o cH N cH3) (cnpcn co and The starting materials for the preparation of the betaines and the sulfobetaines of this invention are the perfiuoroalkylether acid fluorides of the formula R,O[C F O] CF(CF )CFO.
These acid fluorides are available either by the polymerization of hexafluoropropylene oxide or by the polymerization of a mixture of hexafluoropropylene and oxygen.
3 The polymerization of hexafluoropropylene oxide is taught by Moore et al. in U.S. 3,250,808 and the acid fluorides have the structure If hexafluoropropylene oxide alone is polymerized, the products are as described by Moore in Canadian Patent 725,740. If the polymerization of hexafluoropropylene oxide is carried out in the presence of carbonylfluoride (COF or a perfluoroacidfluoride of the formula F CF CFO, the products are of the formula.
where m is -5 as more fully described in French Patent 1,362,548. When the polymerization is carried out in the presence of a perfluoroketone of the formula F z) x 2) F.
as described by Selman in U.S. Pat. 3,274,239, the prod uct is the formula of F(CF2)v where x and y are 1-4 and the total of x+y is 2-5. Thus, R may be a branched or straight-chain perfluoralkyl group of 1-6 carbon atoms.
The acid fluorides prepared by polymerization of mixture of hexafluoropropylene and oxygen are taught by Pasetti, Sianesi and Corti in Die Makromolekulare Chemie 86 pages 308-311 (1965); Sianesi and Fontanelli in Die 'Makrornolekulare Chemie 102 pages 115-124 (1967); and French Patent 1,434,537. The polymerization is carried out at temperatures of about 100 C. to 25 C. in the presence of ultraviolet radiation and the polymeric acid fluorides obtained are best characterized by the formula The above-described perfluoroalkylether acid fluorides are converted to perfluoroalkylether amidoalkylamines of the formula by the reaction of the acid fluoride with a suitable diamine or by the reaction of an alkyl ester derived from the above perfluoroalkylether acid fluoride with the diamine. The formation of perfluoroalkyletheramide by the reaction of perfluoroalkylether acid fluoride with an amine is described by MacKenzie in U.S. Pat. 3,274,244. The reaction is preferably carried out in the presence of inert solvents such as diethylether, tetrahydrofuran, benzene, trichlorotrifluoroethane and the like. Hydrogen fluoride formed in the reaction may be removed by using the amine in excess of that required for the reaction or by using an acid scavenger such as pyridine or triethylamine.
The perfluoroalkylether amidoalkylamines of the formula may also be prepared by first converting the perfluoroalkylether acid fluoride to the corresponding alkylperfluoroalkylether ester and preferably the methyl ester of the formula The esters are prepared by esterification of the corresponding acid fluoride using standard methods, for example, reaction of the acid fluoride with an alkanol such as methanol as taught by Diesslin et al. in U.S. Pat. 2,567,- 011. Preferably, the esterification is carried out by reacting the perfluoroalkylether acid fluoride with excess methanol at -20 C., optionally in an inert solvent, in the presence of suflicient pyridine to consume the hydrogen fluoride formed. In place of methanol one can also use ethanol, propanol, butanol or the like equally well. The alkylperfluoroalkylether esters are then reacted with diamines of the formula HN(R)R N(R )(R to form the perfluoroalkylether amidoalkylamine of the formula R O(C F O),,CF(CF )CON ('R)R N(:R (R
by well-known procedures such as those described in U.S. Pat. 2,764,603.
A large number of diamines of the formula A special procedure is required to obtain a perfluoroalkylether amidoalkylamine wherein R is -CH They are readily prepared by the reaction of the perfluoroalkyletheramide of the formula with formaldehyde and hydrogen chloride to form N- chloromethylperfluoroalkyletheramide of the formula which is then converted to the tertiary amine by the reaction with a secondary amine HN(R (R The betaines and the sulfobetaines of the present invention are then prepared by reacting the above described perfluoroalkyletheramidoalkylamines with salts of haloalkylcarboxylic acid or haloalkyl sulfonic acid. The formation of quaternary ammonium salts by the reaction of a tertiary amine with haloalkyl compounds are well-known and is described for example by Ahlbrecht in U.S. Pat. 2,764,602. Haloalkylcarboxylic acids and haloalkylsulfonic acids from which salts, 'for example the alkali metal salts, are readily obtained, are well-known and useful examples include bromoacetic acid, chloroacetic acid, 2- bromopropionic acid, 3-bromopropionic acid, 2 chloropropionic acid, 3-chloropropionic acid, 3 chlorobutyric acid, 4-chlorobutyric acid, 5 chlorovaleric acid, chloromethylsulfonic acid, 2-bromoethane sulfonic acid, 2- chloroethane sulfonic acid, l-chloroethane sulfonic acid and 3-chloropropane sulfonic acid.
The betaines and the sulfobetaines of the present invention are particularly effective surface active agents in water, and in neutral, strongly acidic and strongly basic aqueous solutions. In contrast to the usual cationic and anionic surface active agents whose activities are markedly altered by the acidic or basic nature of the solutions, the compounds of the present invention are equally eflective in neutral, strongly acidic and strongly basic aqueous solutions. It is clear from the structural feature of the compounds of this invention that the ionic character of the molecule is maintained in neutral, acidic and basic aqueous solutions.
The compounds of this invention are particularly useful in the formation of aqueous foams and in stabilizing such foams after they are formed. The ability to form foams and to stabilize such foams are valuable, for example in fire extinguishant foam formulations. The insensitivity low solid, obtained in 97.4% yield. Elemental analysis showed the following: Percent fluorine calculated 50.6; percent fluorine found 50.7; percent nitrogen calculated 4.4; percent nitrogen found 4.3
of the compounds to the action of acid, alkali or salt 5 Examples 2410 make these compounds particularly valuable smce tlhe Using the procadure of Example 1 and equimolal. 9 f 9 3 upon Contact wlth acld alkah or Salt so amounts of the starting materials listed in Table I the Hons ehmmatedd perfluoroalkyletheramidoalkyl betaines listed in Table I The compounds of this invention are useful in sprea were prepared. In Table A, B C and D have the mean mg aqueous film over the surface of hydrocarbon suring as follows: faces. As is known, when a drop of water is very carefully placed on the surface of a hydrocarbon liquid, the water A:C3F7OCF(CF3) drop remains as a drop on the surface until subsequent B=C F OCF(CF )CF OCF(OF agitation causes it to sink. If a drop of water containing C C F O [CF (CF )CFO'] CF(CF a compound of this invention is placed on the surface of D=C F ()[CF(CF )CF O] CF(CF TABLE I Percent fluorine Percent nitrogen Y m Example Reactants Betaine Galcd Found Calcd Found per ciml: 2 A61CO(])1N(()%)H2)3N(CHQ2 and ACON(H)(OH2)4N(CH9)2CH2CO29 42.3 42.2 5.7 5.8 90.6
a. a BCOl\ l(C2 H5)(CH2)N(CHs)2 BCON(C4H5)(CH2)2N(CH3)2CH2CO2 49.5 49.4 43 4.3 92.4
and ClCHzCOzNa. 4 B3%N(H) (CHz)aN(C2H5)2 and BCON(H) (CH2)3N(C2H5)2CH2C029 48.5 48.2 4.2 4. 1 93.2
3,. 5 n gg riign igo ammonm and BC0N(H)(CHr)sN (CHa)2(CHz)zCOz 49.5 49.3 4.3 42 97.3
a. a is ogg gi-r gd r roaiw(oznazand IB-C0N(H)(CH2)aN (CzHs)z(CHz)2C02 46.8 49.6 41 40 94a 3.. 1 B-6l%%N Ii:I))1(H2)3N(C 4Ho)2 and B-C0N(H)( 2)aN (C4H9)rCH2CO2 44.7 44.5 3.9 3.9 91.3
a. 8 BEfi8HI IgHgCmNw4Hm and B-CON(H)(CH2)aN (G4 9)2(CH2)2COz 43.9 43.8 3.8 3.7 94.2
a. 9 CE{3(1)1NZ(JI%)Hz)4N(GH9)2 and oooN H) oHr 4N oH3 roHzoo2 58.5 58.3 2.5 2.3 92.7
a. 10 DCOII(H(CH2)3N(CH3)2 and D-C0N(H)( 2)aN (CHa)2CH2CO2 60.8 60.4 1.5 1.4 96.3
ClCH2CO2Na.
a hydrocarbon liquid, the water drop immediately spreads E l 11 and covers the hydrocarbon surface with an aqueous film. The ability to form aqueous film in hydrocarbon surface is not a general property of surface active agents. It is not known at present, which structural portion of the compounds of the present invention is responsible for the aqueous film spreading ability but it is believed that the perfluoroalkylether chain of the molecule is involved in this unique characteristic.
The aqueous film spreading property is extremely valuable, particularly in aqueous foam fire extinguishant compositions wherein rapidly covering of burning hydrocarbon surfaces is desirable. After such a fire has been extinguished, it is desirable to maintain foam covering to prevent reignition.
EXAMPLES Example 1 N-dimethylaminopropylamide of perfluoroalkylether acid,
C F OCF(CF )CF OOF(CF 50 g. 0.086 m.) and the sodium salt of chloroacetic acid, ClCH CO Na, 10.1 g. (0.086 m.) and ml. of isopropanol were placed in a 500 ml. reaction flask equipped with a reflux condenser, a thermometer and an agitator. The reaction mixture was heated at reflux (83 C.) with agitation for 16 hours. The reaction mixture was then cooled to room temperature and the precipitated sodium chloride was removed by filtration. The filtrate was transferred to a distillation assembly wherein isopropanol was removed by distillation at reduced pressure. The isopropanol was considered to be completely removed when the contents of the distillation flask reached 50 C. at 5 mm. Hg pressure. The residue in the flask weighing 53.7 g. was the product, which was a very tacky, slightly yel- N-dimethylaminopropylamide of perfluoroalkylether acid,
50 g. (0.086 in.) sodium salt of Z-bromoethanesulfonic acid, Br-CH CH SONa, 18.2 g. (0.086 m.), 300 ml. isopropanol and 300 ml. water were placed in a 1-liter reaction flask equipped with a reflux condenser, a thermometer and an agitator. The reaction mixture was heated at reflux (83 C.) with agitation for 16 hours. The reaction mixture was transferred to a distillation assembly wherein isopropanol and water were removed by distillation at reduced pressures. The residue in the distillation flask was extracted with 300 ml. of isopropanol. The isopropanol extract was then placed in a distillation assembly wherein isopropanol was removed by distillation at reduced pressures. The isopropanol was considered to be completely removed when the contents of the distillation flask reached 50 C. at 5 mm. Hg pressure. The residue in the flask weighing 53.1 g. was the desired product, which was a sticky yellow semi-solid, obtained in 91% yield. The elementary analysis showed the following: Percent fluorine, calculated 46.9, found 46.8; percent nitrogen, calculated 4.1, found 4.0 and percent sulfur, calculated 4.7, found 4.5.
Examples 12 and 13 Using the procedure of Example 11 and equimolar amounts of the starting materials listed in Table II the perfluoroalkyletheramidoalkylsulfobetaines listed in Table II were prepared. In Table II TABLE I1 Percent Percent fluorine nitrogen Yield, Example Reactants Suliobetaiue Calc'd Found Calc'd Found percent 12 B-COH(CH:4)(CH2)3N(CH3)2 BCON(CH3)(CH2)3N (CH3)2(CHz)3SO3 I 45.2 45.4 3.9 3.9 94.2
and Ol(CH2)4SO3Na. 13 DCON(H)(CH2 3N(CH3)2 D-CON(H)(CH2)3N(CH3)z(CHz)zS0 59.3 59.1 1.5 1.3 94.2
and Bl(CH2)zSO3Na.
Examples 14-19 ample. As discussed above, the spreading of an aqueous film on the surface of a hydrocarbon is of particular importance to aqueous fire extinguishant foam formulations. The aqueous film spreading test was carried out by The utility of the compounds of the present invention as surface active agents is clearly demonstrated by the data summarized in Table III below which shows measurements of surface tension of dilute aqueous solutions of carefully Placing 10 drops of the aqueous Solution of the these compounds at 5 using a DuNouy tensiometen 15 compounds on the surface of cyclohexane contained in a It is to be notedthat even at a concentration as low as diameter evaporating dlsh and recording the 0.001% Outstanding reduction in the surface tension is time Seconds) for the cyclohexane surface to be covevident. It is also to be noted that even in the presence ered by the aqueous film. Example 24 is comparative of 5% hydrochloric acid or 5% sodium hydroxide the using the prior art compound of Examples 19 and 21.
TABLE IV .Aq. film 7 Concentration spreadin Example Compound (an/10G ml.) time (see.
22 9 e 0.1 CaF OCF(CF;)CON(H)(CHmN (011020114002 1.0 4
23.; CaF7OCF(CFs)CFaOCF(CF3)CON(H)(CH2)aN (CHa)2CH2CO2 2 24 C7F15CON(H)(CH2)3N(CH3)2(CH2)2CO29 1.0
1 Does not spread. same reduction of surface tension is evident. Example 19 I claim: is comparative using the closest known prior art com- 1. A composition of matter having the chemical forpound. In Table III R;=CF --CF -CF mula TABLE III Compound concentration (g./100 ml.)
Surface tension (dynes/cm.) at 25 0.
Example Compound Medium 0 0.001 0.01 0.1 1.0
14. R1OCF(OF3)CFzOCFCFaCON(C2H5)(C 2)2N (OH:1)2CH2CO2 Water 71.9 15.3 14.7 14.4 15. R40CF(CF3)CF4OCF(CF3)CON(H)(CHmN (O4Ho)2(G 2)zC0z d0 15.4 14.9 14.8 10- R10[CF(CF3)OF2O]4CF(CFa)OONUEI)(CH2):1N (CHa)2CH4COz (In 17 R;OCF(CF3)CF4OCF(CF4)CON(H)(CH2)aN (C a)zCH2C02 "do 18.7 14.8 14.3 5% HCl 72.0 17.2 14.3 14.1 5% NaOH-.. 75.4 17.4 14.5 14.4
18 RioOF CF3 CF2OGF(CF3)CONH(CH2)3N (CH3)2(CH2)ZSO3 -2... Water 71.9 20.1 17.0 16.2 15.5 5% HCl 72.0 22.1 18.4 17.5 16.2 5% NaOH--- 75.4 20.4 17.2 16.4 15.7
19 C7F15CON(H)(CHQSN (CH3)2(CH2)2 02 Y Water 71.9 43.2 28.0 20.0 14.4 5% H01--." 72.0 45.7. 51.0 23.4 15.1 5% NaOH.-. 75.4 43.0 27.9 20.0 14.6
Example 20 C F O[CF(CF )CF O],,CF(CF )CON(R) The utility of the compounds of the present invention wherein I as foaming agents and as foam stabilizers is illustrated in n is an integer of 0 to 8, this example. The testwas conducted by placing 50 ml. R is hydrogen or alkyl of 1 to 6 carbon atoms of a 1% aqueous solut1on of the compound in a 1000 ml. 1 alkylene of 1 to 12 carbon atoms, Erlenmeyer flask, stoppermg the flask and then shaking R218 alkyl of 1 to 6 carbon atoms, the flask vlgorously for 10 seconds. The volume of the R3 is alkyl of 1 to 6 carbon atoms, foam produced, the nature of the foam, and the stability R4 is alkylene of 1 to 4 Carbon atoms and of the foam were observed. Tests with a 1% solution of X CO 0 SO the compound of Example 1 gave a foam volume of 400 15 2 r ml. which was thick and uniform and was stable for References Cited hours.
Example 21 UNITED STATES PATENTS 3,681,413 8/1972 Sweeney et al. 260--501.13 Using the procedure of Example 20 and the prior art 2,764,602 9/1956 Ahlbrecht 260501.13 X compound of Example 19 a 1% aqueous solution of the 3,147,065 9/1964 Kosher et al- 260-5676 M compound gave a foam volume of 800 ml. but the foam was non-uniform with very large bubbles and was un- HOWARD T. MARS, Primary Examiner stable.
Examples 22 24 I M. W. GLYNN, Assistant Examiner The utility of the compounds of the present invention as aqueous film spreading agents is illustrated in this ex- 26501.13, 561 HL; 252-3, 8.0 5, 307, 311, Dig. 7
Claims (1)
1. A COMPOSITION OF MATTER HAVING THE CHEMICAL FORMULA
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00072803A US3839425A (en) | 1970-09-16 | 1970-09-16 | Perfluoroalkyletheramidoalkyl betaines and sulfobetaines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00072803A US3839425A (en) | 1970-09-16 | 1970-09-16 | Perfluoroalkyletheramidoalkyl betaines and sulfobetaines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3839425A true US3839425A (en) | 1974-10-01 |
Family
ID=22109848
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00072803A Expired - Lifetime US3839425A (en) | 1970-09-16 | 1970-09-16 | Perfluoroalkyletheramidoalkyl betaines and sulfobetaines |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3839425A (en) |
Cited By (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3956138A (en) * | 1973-09-24 | 1976-05-11 | Fred Benton Crockett | Compositions of fire-extinguishing foam concentrates and method of using the same |
| US4042522A (en) * | 1975-03-24 | 1977-08-16 | Ciba-Geigy Corporation | Aqueous wetting and film forming compositions |
| US4069244A (en) * | 1975-01-03 | 1978-01-17 | Ciba-Geigy Corporation | Fluorinated amphoteric and cationic surfactants |
| US4099574A (en) * | 1976-04-06 | 1978-07-11 | Chubb Fire Security Limited | Fire-fighting compositions |
| JPS565453A (en) * | 1979-04-06 | 1981-01-20 | Ugine Kuhlmann | Sulfobetaine compound and its use |
| US4430272A (en) | 1981-02-11 | 1984-02-07 | Hoechst Aktiengesellschaft | Fluorine-containing alkylsulfobetaines, a process for their preparation and their use |
| US4469607A (en) * | 1982-04-30 | 1984-09-04 | Mobil Oil Corporation | Pyrrolidinium methane sulfonates as surfactants in enhanced oil recovery |
| US4713182A (en) * | 1986-11-06 | 1987-12-15 | Mine Safety Appliances Company | Fire-fighting foam |
| EP0311473A1 (en) * | 1987-09-16 | 1989-04-12 | Applications Et Transferts De Technologies Avancees Atta | Fluorinated derivate of amino acids, useful as tensioactive or cotensioactive agents, and preparations for biomedical use containing these derivatives |
| JP2001335547A (en) * | 2000-05-26 | 2001-12-04 | Kawaken Fine Chem Co Ltd | Polyoxyalkyleneamide betaine surface active compound and surfactant containing the same |
| US20050054804A1 (en) * | 2003-09-08 | 2005-03-10 | Dams Rudolf J. | Fluorinated polyether isocyanate derived silane compositions |
| US20050096244A1 (en) * | 2003-10-30 | 2005-05-05 | Audenaert Frans A. | Mixture of fluorinated polyethers and use thereof as surfactant |
| US20050121644A1 (en) * | 2003-12-05 | 2005-06-09 | 3M Innovative Properties Company | Coating compositions with perfluoropolyetherisocyanate derived silane and alkoxysilanes |
| US20080114121A1 (en) * | 2006-11-09 | 2008-05-15 | E. I. Du Pont De Nemours And Company | Aqueous Polymerization of Fluorinated Monomers Using Polymerization Agent Comprising Fluoropolyether Acid or Salt and Hydrocarbon Surfactant |
| US20080114122A1 (en) * | 2006-11-09 | 2008-05-15 | E. I. Du Pont De Nemours And Company | Aqueous Polymerization of Fluorinated Monomer Using Polymerization Agent Comprising High Molecular Weight Fluoropolyether Acid or Salt and Fluoropolyether Acid or Salt Surfactant |
| US20090281241A1 (en) * | 2008-05-09 | 2009-11-12 | E. I. Du Pont De Nemours And Company | Aqueous Polymerization of Fluorinated Monomer Using a Mixture of Fluoropolyether Acids or Salts |
| WO2011005672A2 (en) | 2009-07-09 | 2011-01-13 | 3M Innovative Properties Company | Methods for treating carbonate hydrocarbon-bearing formations with fluorinated amphoteric compounds |
| US7943567B2 (en) | 2004-01-30 | 2011-05-17 | E.I. Du Pont De Nemours And Company | Production processes and systems, compositions, surfactants, monomer units, metal complexes, phosphate esters, glycols, aqueous film forming foams, and foam stabilizers |
| US7977438B2 (en) | 2006-11-09 | 2011-07-12 | E. I. Du Pont De Nemours And Company | Aqueous polymerization of fluorinated monomers using polymerization agent comprising fluoropolyether acid or salt and siloxane surfactant |
| WO2012045080A1 (en) | 2010-10-01 | 2012-04-05 | Tyco Fire Products Lp | Aqueous fire-fighting foams with reduced fluorine content |
| US8318656B2 (en) | 2007-07-03 | 2012-11-27 | E. I. Du Pont De Nemours And Company | Production processes and systems, compositions, surfactants, monomer units, metal complexes, phosphate esters, glycols, aqueous film forming foams, and foam stabilizers |
| US8338517B2 (en) | 2007-05-23 | 2012-12-25 | 3M Innovative Properties Company | Aqueous compositions of fluorinated surfactants and methods of using the same |
| US8476385B2 (en) | 2007-06-06 | 2013-07-02 | 3M Innovative Properties Company | Fluorinated ether compositions and methods of using the same |
| US8629089B2 (en) | 2008-12-18 | 2014-01-14 | 3M Innovative Properties Company | Method of contacting hydrocarbon-bearing formations with fluorinated ether compositions |
| US8633288B2 (en) | 2008-07-18 | 2014-01-21 | 3M Innovative Properties Company | Fluorinated ether compounds and methods of using the same |
| WO2014144988A2 (en) | 2013-03-15 | 2014-09-18 | Tyco Fire Products Lp | Perfluoroalkyl composition with reduced chain length |
| WO2014153140A1 (en) | 2013-03-14 | 2014-09-25 | Tyco Fire & Security Gmbh | Trimethylglycine as a freeze suppressant in fire fighting foams |
| WO2016130810A1 (en) | 2015-02-13 | 2016-08-18 | Tyco Fire Products Lp | Use of an indicator as a marker in foam concentrates |
| WO2017161162A1 (en) | 2016-03-18 | 2017-09-21 | Tyco Fire Products Lp | Organosiloxane compounds as active ingredients in fluorine free fire suppression foams |
| WO2017161156A1 (en) | 2016-03-18 | 2017-09-21 | Tyco Fire Products Lp | Polyorganosiloxane compounds as active ingredients in fluorine free fire suppression foams |
| CN107469731A (en) * | 2017-08-28 | 2017-12-15 | 江苏理文化工有限公司 | A kind of sulfonic fluoropolymer type zwitterionic surfactant and preparation method |
| WO2018022763A1 (en) | 2016-07-29 | 2018-02-01 | Tyco Fire Products Lp | Firefighting foam compositions containing deep eutectic solvents |
| CN108884385A (en) * | 2016-04-01 | 2018-11-23 | 3M创新有限公司 | Quantum dots with stabilized fluorochemical reagents |
| JP2018193373A (en) * | 2012-07-18 | 2018-12-06 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | Fluorosurfactants |
| US10870030B2 (en) | 2014-04-02 | 2020-12-22 | Tyco Fire Products Lp | Fire extinguishing compositions and method |
-
1970
- 1970-09-16 US US00072803A patent/US3839425A/en not_active Expired - Lifetime
Cited By (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3956138A (en) * | 1973-09-24 | 1976-05-11 | Fred Benton Crockett | Compositions of fire-extinguishing foam concentrates and method of using the same |
| US4069244A (en) * | 1975-01-03 | 1978-01-17 | Ciba-Geigy Corporation | Fluorinated amphoteric and cationic surfactants |
| US4161602A (en) * | 1975-01-03 | 1979-07-17 | Ciba-Geigy Corporation | Fluorinated amphoteric and cationic surfactants containing a pyridinium moiety |
| US4042522A (en) * | 1975-03-24 | 1977-08-16 | Ciba-Geigy Corporation | Aqueous wetting and film forming compositions |
| US4099574A (en) * | 1976-04-06 | 1978-07-11 | Chubb Fire Security Limited | Fire-fighting compositions |
| JPS6221778B2 (en) * | 1979-04-06 | 1987-05-14 | Atokemu Soc | |
| JPS565453A (en) * | 1979-04-06 | 1981-01-20 | Ugine Kuhlmann | Sulfobetaine compound and its use |
| US4430272A (en) | 1981-02-11 | 1984-02-07 | Hoechst Aktiengesellschaft | Fluorine-containing alkylsulfobetaines, a process for their preparation and their use |
| US4469607A (en) * | 1982-04-30 | 1984-09-04 | Mobil Oil Corporation | Pyrrolidinium methane sulfonates as surfactants in enhanced oil recovery |
| US4713182A (en) * | 1986-11-06 | 1987-12-15 | Mine Safety Appliances Company | Fire-fighting foam |
| EP0311473A1 (en) * | 1987-09-16 | 1989-04-12 | Applications Et Transferts De Technologies Avancees Atta | Fluorinated derivate of amino acids, useful as tensioactive or cotensioactive agents, and preparations for biomedical use containing these derivatives |
| JP2001335547A (en) * | 2000-05-26 | 2001-12-04 | Kawaken Fine Chem Co Ltd | Polyoxyalkyleneamide betaine surface active compound and surfactant containing the same |
| JP4562243B2 (en) * | 2000-05-26 | 2010-10-13 | 川研ファインケミカル株式会社 | Polyoxyalkylene amide betaine type surfactant compound and surfactant containing the same |
| US7652115B2 (en) | 2003-09-08 | 2010-01-26 | 3M Innovative Properties Company | Fluorinated polyether isocyanate derived silane compositions |
| US20050054804A1 (en) * | 2003-09-08 | 2005-03-10 | Dams Rudolf J. | Fluorinated polyether isocyanate derived silane compositions |
| US20050096244A1 (en) * | 2003-10-30 | 2005-05-05 | Audenaert Frans A. | Mixture of fluorinated polyethers and use thereof as surfactant |
| US7141537B2 (en) * | 2003-10-30 | 2006-11-28 | 3M Innovative Properties Company | Mixture of fluorinated polyethers and use thereof as surfactant |
| US20050121644A1 (en) * | 2003-12-05 | 2005-06-09 | 3M Innovative Properties Company | Coating compositions with perfluoropolyetherisocyanate derived silane and alkoxysilanes |
| US7803894B2 (en) | 2003-12-05 | 2010-09-28 | 3M Innovatie Properties Company | Coating compositions with perfluoropolyetherisocyanate derived silane and alkoxysilanes |
| US7943567B2 (en) | 2004-01-30 | 2011-05-17 | E.I. Du Pont De Nemours And Company | Production processes and systems, compositions, surfactants, monomer units, metal complexes, phosphate esters, glycols, aqueous film forming foams, and foam stabilizers |
| US7705074B2 (en) | 2006-11-09 | 2010-04-27 | E. I. Du Pont De Nemours And Company | Aqueous polymerization of fluorinated monomer using polymerization agent comprising fluoropolyether acid or salt and short chain fluorosurfactant |
| US20080269408A1 (en) * | 2006-11-09 | 2008-10-30 | E. I. Du Pont De Nemours And Company | Aqueous Polymerization of Fluorinated Monomer Using Polymerization Agent Comprising Fluoropolyether Acid or Salt and Short Chain Fluorosurfactant |
| US20080114122A1 (en) * | 2006-11-09 | 2008-05-15 | E. I. Du Pont De Nemours And Company | Aqueous Polymerization of Fluorinated Monomer Using Polymerization Agent Comprising High Molecular Weight Fluoropolyether Acid or Salt and Fluoropolyether Acid or Salt Surfactant |
| US20080114121A1 (en) * | 2006-11-09 | 2008-05-15 | E. I. Du Pont De Nemours And Company | Aqueous Polymerization of Fluorinated Monomers Using Polymerization Agent Comprising Fluoropolyether Acid or Salt and Hydrocarbon Surfactant |
| US8519072B2 (en) | 2006-11-09 | 2013-08-27 | E I Du Pont De Nemours And Company | Aqueous polymerization of fluorinated monomer using polymerization agent comprising fluoropolyether acid or salt and short chain fluorosurfactant |
| US7897682B2 (en) | 2006-11-09 | 2011-03-01 | E. I. Du Pont De Nemours And Company | Aqueous polymerization of fluorinated monomers using polymerization agent comprising fluoropolyether acid or salt and hydrocarbon surfactant |
| US7932333B2 (en) | 2006-11-09 | 2011-04-26 | E.I. Du Pont De Nemours And Company | Aqueous polymerization of fluorinated monomer using polymerization agent comprising high molecular weight fluoropolyether acid or salt and fluoropolyether acid or salt surfactant |
| US11440981B2 (en) | 2006-11-09 | 2022-09-13 | The Chemours Company Fc, Llc | Aqueous polymerization of fluorinated monomer using polymerization agent comprising fluoropolyether acid or salt and short chain fluorosurfactant |
| US7977438B2 (en) | 2006-11-09 | 2011-07-12 | E. I. Du Pont De Nemours And Company | Aqueous polymerization of fluorinated monomers using polymerization agent comprising fluoropolyether acid or salt and siloxane surfactant |
| US8338517B2 (en) | 2007-05-23 | 2012-12-25 | 3M Innovative Properties Company | Aqueous compositions of fluorinated surfactants and methods of using the same |
| US8476385B2 (en) | 2007-06-06 | 2013-07-02 | 3M Innovative Properties Company | Fluorinated ether compositions and methods of using the same |
| US8318656B2 (en) | 2007-07-03 | 2012-11-27 | E. I. Du Pont De Nemours And Company | Production processes and systems, compositions, surfactants, monomer units, metal complexes, phosphate esters, glycols, aqueous film forming foams, and foam stabilizers |
| US9732212B2 (en) | 2008-05-09 | 2017-08-15 | The Chemours Company Fc, Llc | Aqueous polymerization of fluorinated monomer using a mixture of fluoropolyether acids or salts |
| US20090281241A1 (en) * | 2008-05-09 | 2009-11-12 | E. I. Du Pont De Nemours And Company | Aqueous Polymerization of Fluorinated Monomer Using a Mixture of Fluoropolyether Acids or Salts |
| US8633288B2 (en) | 2008-07-18 | 2014-01-21 | 3M Innovative Properties Company | Fluorinated ether compounds and methods of using the same |
| US8629089B2 (en) | 2008-12-18 | 2014-01-14 | 3M Innovative Properties Company | Method of contacting hydrocarbon-bearing formations with fluorinated ether compositions |
| WO2011005672A2 (en) | 2009-07-09 | 2011-01-13 | 3M Innovative Properties Company | Methods for treating carbonate hydrocarbon-bearing formations with fluorinated amphoteric compounds |
| US8833449B2 (en) | 2009-07-09 | 2014-09-16 | 3M Innovative Properties Company | Methods for treating carbonate hydrocarbon-bearing formations with fluorinated amphoteric compounds |
| US9669246B2 (en) | 2010-10-01 | 2017-06-06 | Tyco Fire Products Lp | Aqueous fire-fighting foams with reduced fluorine content |
| WO2012045080A1 (en) | 2010-10-01 | 2012-04-05 | Tyco Fire Products Lp | Aqueous fire-fighting foams with reduced fluorine content |
| US10328297B2 (en) | 2010-10-01 | 2019-06-25 | Tyco Fire Products Lp | Aqueous fire-fighting foams with reduced fluorine content |
| JP2018193373A (en) * | 2012-07-18 | 2018-12-06 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングＭｅｒｃｋ Ｐａｔｅｎｔ Ｇｅｓｅｌｌｓｃｈａｆｔ ｍｉｔ ｂｅｓｃｈｒａｅｎｋｔｅｒ Ｈａｆｔｕｎｇ | Fluorosurfactants |
| WO2014153140A1 (en) | 2013-03-14 | 2014-09-25 | Tyco Fire & Security Gmbh | Trimethylglycine as a freeze suppressant in fire fighting foams |
| US10369395B2 (en) | 2013-03-14 | 2019-08-06 | Tyco Fire Products Lp | Trimethylglycine as a freeze suppressant in fire fighting foams |
| WO2014144988A2 (en) | 2013-03-15 | 2014-09-18 | Tyco Fire Products Lp | Perfluoroalkyl composition with reduced chain length |
| US11766582B2 (en) | 2014-04-02 | 2023-09-26 | Tyco Fire Products Lp | Fire extinguishing compositions and method |
| US11305143B2 (en) | 2014-04-02 | 2022-04-19 | Tyco Fire Products Lp | Fire extinguishing compositions and method |
| US10870030B2 (en) | 2014-04-02 | 2020-12-22 | Tyco Fire Products Lp | Fire extinguishing compositions and method |
| WO2016130810A1 (en) | 2015-02-13 | 2016-08-18 | Tyco Fire Products Lp | Use of an indicator as a marker in foam concentrates |
| US10786696B2 (en) | 2015-02-13 | 2020-09-29 | Tyco Fire Products Lp | Use of an indicator as a marker in foam concentrates |
| US10780305B2 (en) | 2016-03-18 | 2020-09-22 | Tyco Fire Products Lp | Organosiloxane compounds as active ingredients in fluorine free fire suppression foams |
| US11173334B2 (en) | 2016-03-18 | 2021-11-16 | Tyco Fire Products Lp | Polyorganosiloxane compounds as active ingredients in fluorine free fire suppression foams |
| WO2017161156A1 (en) | 2016-03-18 | 2017-09-21 | Tyco Fire Products Lp | Polyorganosiloxane compounds as active ingredients in fluorine free fire suppression foams |
| WO2017161162A1 (en) | 2016-03-18 | 2017-09-21 | Tyco Fire Products Lp | Organosiloxane compounds as active ingredients in fluorine free fire suppression foams |
| CN108884385A (en) * | 2016-04-01 | 2018-11-23 | 3M创新有限公司 | Quantum dots with stabilized fluorochemical reagents |
| CN108884385B (en) * | 2016-04-01 | 2021-08-27 | 3M创新有限公司 | Quantum dots with stabilized fluorochemical reagents |
| WO2018022763A1 (en) | 2016-07-29 | 2018-02-01 | Tyco Fire Products Lp | Firefighting foam compositions containing deep eutectic solvents |
| US11771938B2 (en) | 2016-07-29 | 2023-10-03 | Tyco Fire Products Lp | Firefighting foam compositions containing deep eutectic solvents |
| CN107469731B (en) * | 2017-08-28 | 2020-01-24 | 江苏理文化工有限公司 | Fluorine-containing sulfonic acid type zwitterionic surfactant and preparation method thereof |
| CN107469731A (en) * | 2017-08-28 | 2017-12-15 | 江苏理文化工有限公司 | A kind of sulfonic fluoropolymer type zwitterionic surfactant and preparation method |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3839425A (en) | Perfluoroalkyletheramidoalkyl betaines and sulfobetaines | |
| US2567011A (en) | Fluorocarbon acids and derivatives | |
| AU723935B2 (en) | Aqueous film-forming foam compositions | |
| US3721706A (en) | Perfluoro-alkyl-alkylene-sulfonamidoalkylene-dialkylamines and their quaternary ammonium salts | |
| US3419595A (en) | Fluorocarbon fluoroalkanesulfonates | |
| JP2002514190A (en) | α-Branched fluoroalkylcarbonyl fluoride and its derivatives | |
| US3238236A (en) | N-(monochloro-perfluoro-higher alkanoyl)amino-lower carboxylic acids | |
| US2593737A (en) | Perfluorinated cyclohexyl carboxylic acid and cyclohexyl acetic acid and derivatives | |
| DE69113695T2 (en) | Process for the preparation of perfluoroalkoxysulfone compounds. | |
| US2403207A (en) | Chemical process and products | |
| US2691043A (en) | Fluorinated amines | |
| US4278552A (en) | Fluorine-containing betaine compounds, and production and use thereof | |
| EP0885184B1 (en) | Perfluoro(alkoxycycloalkane)carbonyl fluoride compositions and their use | |
| US4167639A (en) | Fluorinated sulfosuccinates | |
| US3944610A (en) | N,N-bis-aminoalkylamides of polyoxaperfluoroalkandioic acids, derivatives thereof and process for preparing same | |
| US4209456A (en) | Fluorine-containing alkyl-sulfato-betaines and processes for their manufacture | |
| KR20000052962A (en) | Aqueous fluoropolymer compositions and method of preparing the same | |
| US3681413A (en) | Quaternary ammonium compounds | |
| EP0070635B1 (en) | Beta-substituted polyfluoropropionate salts and derivatives | |
| US4146736A (en) | Process for the manufacture of ethers | |
| JPH06503348A (en) | Method for producing fluoroaliphatic aminocarboxylate surfactant | |
| US3232970A (en) | Terminally branched and terminally monochlorinated perfluorocarboxylic acids | |
| JPS629586B2 (en) | ||
| US3821290A (en) | Polyfluoroisoalkoxyalkyl sulfonic acids | |
| JPS6113863B2 (en) |