Patent Application
20190352237
The present invention relates to a fluorine-containing composition for masonry treatment. Particularly the present invention relates to an anionic fluorine-containing treatment composition which gives the excellent water- and oil-repellency and soil resistance (contamination resistance) to a porous substrate (masonry substrate) which has micropores, such as stone, tile and concrete.
Hitherto, a cationic treatment agent comprising an amino group-containing copolymerizable monomer is known as a masonry treatment composition (for example, WO 2009/075387 (JP2011/506621 A)). JP2010-90286 A discloses an anionic treatment agent containing a silicon-containing unsaturated compound and carboxylic acid group.
On the other hand, WO2011/027877 (JP2013-503267 A) discloses a treatment agent for paper which comprises a copolymer comprising a carboxylic acid group-containing monomer. However, the use for treatment of masonry is not disclosed at all. In the treatment of paper, oil repellency is important and high water repellency is not required. WO2011/027877 does not describe a means for imparting the high water repellency required for masonry treatment.
The cationic treatment agent comprising an amino group-containing copolymerizable monomer had the problem that stability (storage stability) is poor, in case of a mixture with an additive for enhancing adhesion or permeability with a substrate. In addition, since cement was strongly alkaline, the cationic treatment agent gives the problems that the whitening of concrete occurs when the cationic treatment agent is applied to the concrete so that the cationic treatment agent cannot be used.
On the other hand, the conventional anionic treatment agents do not have satisfactory water- and oil-repellency given to various masonries.
The masonry treatment agent is needed, which has both of the high storage stability of the treatment agent and the sufficient water- and oil-repellency.
Patent Document 1: WO2009/075387 (JP 2011/506621 A)
Patent Document 2: JP2010-90286 A
Patent Document 3: WO2011/027877 (JP2013-503267 A)
An object of the present invention is to provide an anionic treatment agent which gives both of high storage stability and high water- and oil-repellency to masonry.
The present invention provides a masonry treatment composition comprising a fluorine-containing polymer comprising repeating units derived from:
(a) a fluorine-containing monomer having a fluoroalkyl group represented by the general formula:
CH2═C(—X)—C(═O)—Y—Z—Rf
wherein X is a hydrogen atom, a linear or branched C1-C21 alkyl group, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a CFX1X2 group wherein X1 and X2 are a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom or an iodine atom, a cyano group, a linear or branched C1-C21 fluoroalkyl group, a substituted or non-substituted benzyl group, or a substituted or non-substituted phenyl group;
Y is —O— or —NH—;
Z is a C1-C10 aliphatic group, a C6-C10 aromatic or cycloaliphatic group, a —CH2CH2N(R1)SO2— group wherein R1 is a C1-C4 alkyl group, a —CH2CH(OZ1) CH2— group wherein Z1 is a hydrogen atom or an acetyl group, or a —(CH2)m—SO2—(CH2)n— group or a —(CH2)m—S—(CH2)n— group wherein m is 1 to 10 and n is 0 to 10, and
Rf is a C1-C6 linear or branched fluoroalkyl group,
(b) a first hydrophilic monomer represented by the general formula:
CH2═CX11C(═O)—O—RO—X12
wherein X11 is a hydrogen atom or a methyl group,
X12 is a hydrogen atom or a saturated or unsaturated C1-C22 hydrocarbon group, and
R is a C2-C6 alkylene group,
(c) a second hydrophilic monomer represented by the general formula:
CH2═CX21C(═O)—O—(RO)n—X22
or
CH2═CX31C(═O)—O—(RO)n—C(═O)CX32═CH2
wherein each of X21, X31 and X32 is independently a hydrogen atom or a methyl group,
X22 is a hydrogen atom or a saturated or unsaturated C1-C22 hydrocarbon group,
R is a C2-C6 alkylene group, and
n is an integer of 2 to 90, and
(d) a monomer having an anion-donating group and an ethylenically unsaturated double bond.
The present invention also provides a method of treating masonry with the above-mentioned masonry treatment composition, and masonry treated with the above-mentioned masonry treatment composition.
In the present invention, the fluorine-containing polymer enhances the storage stability at the time of a combination with an anionic additive by using the anion-donating group-containing monomer. The dispersibility in water of the fluorine-containing polymer is improved and the permeability into the masonry of the treatment agent is good. The treatment agent of the present invention gives high soil resistance (high resistance to contamination) to masonry in addition to high water- and oil-repellency.
In the present invention, the ingredients of the fluorine-containing copolymer have a great influence on the properties of the masonry treatment composition.
The masonry treatment agent of the present invention has the repeating units derived from the fluorine-containing monomer (a), the first hydrophilic monomer (b), the second hydrophilic monomer (c), and the anion-donating group-containing monomer (d).
The fluorine-containing monomer (a) is at least one compound represented by the general formula:
CH2═C(—X)—C(═O)—Y—Z—Rf
wherein X is a hydrogen atom, a linear or branched C1-C21 alkyl group, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a CFX1X2 group (wherein X1 and X2 are a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom or an iodine atom), a cyano group, a linear or branched C1-C21 fluoroalkyl group, a substituted or non-substituted benzyl group, or a substituted or non-substituted phenyl group;
Y is —O— or —NH—;
Z is a C1-C10 aliphatic group, a C6-C10 aromatic or cycloaliphatic group, a —CH2CH2N(R1)SO2— group wherein R1 is a C1-C4 alkyl group, a —CH2CH(OZ1) CH2— group wherein Z1 is a hydrogen atom or an acetyl group, or a —(CH2)m—SO2—(CH2)n— group or a —(CH2)m—S—(CH2)n— group wherein m is 1 to 10 and n is 0 to 10, and
Rf is a C1-C06 linear or branched fluoroalkyl group.
Preferably, the fluorine-containing monomer (a) is an acrylate wherein Y is —O—.
The fluorine-containing monomer (a) may be substituted by, for example, a halogen atom at α-position of acrylate or methacrylate. Therefore, X may be a linear or branched C2-C21 alkyl group, a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a CFX1X2 group (wherein X1 and X2 are a hydrogen atom, a fluorine atom, a chlorine atom, a bromine atom or an iodine atom), a cyano group, a linear or branched C1-C21 fluoroalkyl group, a substituted or non-substituted benzyl group, or a substituted or non-substituted phenyl group.
Preferably, X is a linear or branched C1-C21 alkyl group or a chlorine atom, more preferably a methyl group or a chlorine atom. Particularly preferably, X is a methyl group in view of high water repellency.
The Rf group is preferably a perfluoroalkyl group. The carbon number of the Rf group may be 1 to 6, particularly 4 to 6, especially 6. Examples of the Rf group include —CF3, —CF2CF3, —CF2CF2CF3, —CF(CF3)2, —CF2CF2CF2CF3, —CF2CF(CF3)2, —C(CF3)3, —(CF2)4 CF3, —(CF2)2CF(CF3)2, —CF2C(CF3)3, —CF(CF3)CF2CF2CF3, —(CF2)5CF3 and —(CF2)3CF(CF3)2. Especially, —(CF2)5CF3 is preferable.
Preferably, the Rf group is a perfluoroalkyl group having 4 to 6, for example, 6 carbon atoms, since good water- and oil-repellency and soil resistance are obtained.
Examples of the fluorine-containing monomer (a) include the followings:
Rf—(CH2)10OCOCH═CH2
Rf—(CH2)10OCOC(CH3)═CH2
Rf—CH2OCOCH═CH2
Rf—CH2OCOC(CH3)═CH2
Rf—(CH2)2OCOCH═CH2
Rf—(CH2)2OCOC(CH3)═CH2
Rf—SO2N(CH3)(CH2)2OCOCH═CH2
Rf—SO2N(C2H5)(CH2)2OCOCH═CH2
Rf—CH2CH(OCOCH3)CH2OCOC(CH3)═CH2
Rf—CH2CH(OH)CH2OCOCH═CH2
Other examples of the fluorine-containing monomer (a), which do not limit the fluorine-containing monomer (a), include the followings:
CH2═C(—H)—C(═O)—O—C6H4—Rf
CH2═C(—Cl)—C(═O)—O—(CH2)2—Rf
CH2═C(—H)—C(═O)—O—(CH2)2N(—CH3)SO2—Rf
CH2═C(—H)—C(═O)—O—(CH2)2N(—C2H5) SO2—Rf
CH2═C(—H)—C(═O)—O—CH2CH(—OH) CH2—Rf
CH2═C(—H)—C(═O)—O—CH2CH(—OCOCH3) CH2—Rf
CH2═C(—H)—C(═O)—O—(CH2)2—S—Rf
CH2═C(—H)—C(═O)—O—(CH2)2—S—(CH2)2—Rf
CH2═C(—H)—C(═O)—O—(CH2)3—SO2—Rf
CH2═C(—H)—C(═O)—O—(CH2)2—SO2—(CH2)2—Rf
CH2═C(—H)—C(═O)—NH—(CH2)2—Rf
CH2═C(—CH3)—C(═O)—O—(CH2)2—S—Rf
CH2═C(—CH3)—C(═O)—O—(CH2)2—S—(CH2)2—Rf
CH2═C(—CH3)—C(═O)—O—(CH2)3—SO2—Rf
CH2═C(—CH3)—C(═O)—O—(H2)2—SO2—(CH2)2—Rf
CH2═C(—CH3)—C(═O)—NH—(CH2)2—Rf
CH2═C(—F)—C(═O)—O—(CH2)2—S—Rf
CH2═C(—F)—C(═O)—O—(CH2)2—S—(CH2)2—Rf
CH2═C(—F)—C(═O)—O—(CH2)2—SO2—Rf
CH2═C(—F)—C(═O)—O—(CH2)2—SO2—(CH2)2—Rf
CH2═C(—F)—C(═O)—NH—(CH2)2—Rf
CH2═C(—Cl)—C(═O)—O—(CH2)2—S—Rf
CH2═C(—Cl)—C(═O)—O—(CH2)2—S—(CH2)2—Rf
CH2═C(—Cl)—C(═O)—O—(CH2)2—SO2—Rf
CH2═C(—Cl)—C(═O)—O—(CH2)2—SO2—(CH2)2—Rf
CH2═C(—Cl)—C(═O)—NH—(CH2)2—Rf
CH2═C(—CF3)—C(═O)—O—(CH2)2—S—Rf
CH2═C(—CF3)—C(═O)—O—(CH2)2—S—(C H2)2—Rf
CH2═C(—CF3)—C(═O)—O—(CH2)2—SO2—Rf
CH2═C(—CF3)—C(═O)—O—(CH2)2—SO2—(CH2)2—Rf
CH2═C(—CF3)—C(═O)—NH—(CH2)2—Rf
CH2═C(—CF2H)—C(═O)—O—(CH2)2—S—Rf
CH2═C(—CF2H)—C(═O)—O—(CH2)2—S—(CH2)2—Rf
CH2═C(—CF2H)—C(═O)—O—(CH2)2—SO2—Rf
CH2═C(—CF2H)—C(═O)—O—(CH2)2—SO2—(C H2)2—Rf
CH2═C(—CF2H)—C(═O)—NH—(CH2)2—Rf
CH2═C(—CN)—C(═O)—O—(CH2)2—S—Rf
CH2═C(—CN)—C(═O)—O—(CH2)2—S—(CH2)2—Rf
CH2═C(—CN)—C(═O)—O—(CH2)2—SO2—Rf
CH2═C(—CN)—C(═O)—O—(CH2)2—SO2—(CH2)2—Rf
CH2═C(—CN)—C(═O)—NH—(CH2)2—Rf
CH2═C(—CF2CF3)—C(═O)—O—(CH2)2—S—Rf
CH2═C(—CF2CF3)—C(═O)—O—(CH2)2—S—(CH2)2—Rf
CH2═C(—CF2CF3)—C(═O)—O—(CH2)2—SO2—Rf
CH2═C(—CF2CF3)—C(═O)—O—(CH2)2—SO2—(C H2)2—Rf
CH2═C(—CF2CF3)—C(═O)—NH—(CH2)2—Rf
CH2═C(—F)—C(═O)—O—(CH2)3—S—Rf
CH2═C(—F)—C(═O)—O—(CH2)3—S—(CH2)2—Rf
CH2═C(—F)—C(═O)—O—(CH2)3—SO2—Rf
CH2═C(—F)—C(═O)—O—(CH2)3—SO2—(CH2)2—Rf
CH2═C(—F)—C(═O)—NH—(CH2)3—Rf
CH2═C(—Cl)—C(═O)—O—(CH2)3—S—Rf
CH2═C(—Cl)—C(═O)—O—(CH2)3—S—(CH2)2—Rf
CH2═C(—Cl)—C(═O)—O—(CH2)3—SO2—Rf
CH2═C(—Cl)—C(═O)—O—(CH2)3—SO2—(CH2)2—Rf
CH2═C(—CF3)—C(═O)—O—(CH2)3—S—Rf
CH2═C(—CF3)—C(═O)—O—(CH2)3—S—(CH2)2—Rf
CH2═C(—CF3)—C(═O)—O—(CH2)3—SO2—Rf
CH2═C(—CF3)—C(═O)—O—(CH2)3—SO2—(CH2)2—Rf
CH2═C(—CF2H)—C(═O)—O—(CH2)3—S—Rf
CH2═C(—CF2H)—C(═O)—O—(CH2)3—S—(CH2)2—Rf
CH2═C(—CF2H)—C(═O)—O—(CH2)3—SO2—Rf
CH2═C(—CF2H)—C(═O)—O—(CH2)3—SO2—(C H2)2—Rf
CH2═C(—CN)—C(═O)—O—(CH2)3—S—Rf
CH2═C(—CN)—C(═O)—O—(CH2)3—S—(CH2)2—Rf
CH2═C(—CN)—C(═O)—O—(CH2)3—SO2—Rf
CH2═C(—CN)—C(═O)—O—(CH2)3—SO2—(CH2)2—Rf
CH2═C(—CF2CF3)—C(═O)—O—(CH2)3—S—Rf
CH2═C(—CF2CF3)—C(═O)—O—(CH2)3—S—(CH2)2—Rf
CH2═C(—CF2CF3)—C(═O)—O—(CH2)3—SO2—Rf
CH2═C(—CF2CF3)—C(═O)—O—(CH2)2—SO2—(CH2)2—Rf
wherein Rf is a C1-C06 fluoroalkyl group, preferably a C4-C6 fluoroalkyl group.
The first hydrophilic monomer (b) is at least one compound represented by the general formula:
CH2═CX11C(═O)—O—RO—X12
wherein X11 is a hydrogen atom or a methyl group,
X12 is a hydrogen atom or a saturated or unsaturated C1-C22 hydrocarbon group, and
R is a C2-C6 alkylene group.
The first hydrophilic monomer (b) is a mono-oxyalkylene (meth)acrylate. Preferably, the number of carbon atoms in the oxyalkylene group is 2 to 4, particularly 2, in view of water solubility.
Specific examples of the first hydrophilic monomer (b) include: CH2═CH—C(═O)—O—CH2CH2OH, CH2═C(CH3)—C(═O)—O—CH2CH2OH CH2═CH—C(═O)—O—CH2CH2OCH3, and CH2═C(CH3)—C(═O)—O—CH2CH2OCH3.
The second hydrophilic monomer (c) is at least one compound represented by the general formula:
CH2═CX21C(═O)—O—(RO)n—X22
or
CH2═CX31C(═O)—O—(RO)n—C(═O)CX32═CH2
wherein each of X21, X31 and X32 is independently a hydrogen atom or a methyl group,
X22 is a hydrogen atom or a saturated or unsaturated C1-C22 hydrocarbon group,
R is a C2-C6 alkylene group, and
n is an integer of 2 to 90.
The second hydrophilic monomer (c) is a polyoxyalkylene (meth)acrylate. The second hydrophilic monomer (c) may be ω-hydroxy-polyoxyalkylene (meth)acrylate. Preferably, the number of carbon atoms in the oxyalkylene group is 2 to 4, particularly 2, in view of water solubility. An average degree of polymerization of the oxyalkylene group in a polyoxyalkylene group may be 2 to 10, preferably 2 to 5.
Specific examples of the second hydrophilic monomer (c) include:
CH2═CH—C(═O)—O—(CH2CH2O)2H,
CH2═CH—C(═O)—O—(CH2CH2O)3H,
CH2═CH—C(═O)—O—(CH2CH2O)11H,
CH2═CH—C(═O)—O—(CH2CH2O)12H,
CH2═C(CH3)—C(═O)—O—(CH2CH2O)2H,
CH2═C(CH3)—C(═O)—O—(CH2CH2O)3H,
CH2═C(CH3)—C(═O)—O—(CH2CH2O)11H,
CH2═C(CH3)—C(═O)—O—(CH2CH2O)12H,
CH2═CH—C(═O)—O—(CH2)2—OCH3,
CH2═CH—C(═O)—O—(CH2)2—OCH2CH3,
CH2═C(CH3)—C(═O)—O—(CH2)2—OCH3,
CH2═C(CH3)—C(═O)—O—(CH2)2—CH2CH3,
CH2═CH—C(═O)—O—(CH2CH2O)2C(═O)—CH═CH2, and
CH2═C(CH3)—C(═O)—O—(CH2CH2O)2C(═O)—CH═CH2.
Both of high water solubility and high water repellency can be obtained by using a combination of the first hydrophilic monomer (b) and the second hydrophilic monomer (c). Preferably, a weight ratio of the first hydrophilic monomer (b) and the second hydrophilic monomer (c) is 9:1 to 1:9, particularly 8:2 to 5:5.
The anion-donating group-containing monomer (d) is a compound having an anion-donating group and an ethylenically unsaturated double bond (a carbon-carbon double bond). The anion-donating group may be a carboxyl group or a sulfonic acid group. Preferably, the anion-donating group is a carboxyl group. Specific examples of the monomer (d) include (meth)acrylic acid, crotonic acid, maleic acid, fumaric acid, itaconic acid, citraconic acid, vinylsulfonic acid, (meth)allylsulfonic acid, styrene sulfonic acid, vinylbenzene sulfonic acid, acrylamide-tert-butylsulfonic acid, and salts thereof. Particularly preferably, the monomer (d) is (meth)acrylic acid, in view of copolymerizability. (Meth)acrylic acid enhances the water solubility of the fluorine-containing polymer, and gives high storage stability of the treatment agent and high permeability into the substrate.
Each of the monomers (a) to (d) may be alone or a combination of at least two. Although the monomers constituting the fluorine-containing polymer may comprise an amino group-containing monomer, it is preferable that the monomers do not comprise the amino group-containing monomer.
In the fluorine-containing polymer, the amount of the fluorine-containing monomer (a) may be 40 to 90% by weight, the amount of a monomer (b) may be 2 to 30% by weight, the amount of a monomer (c) may be 2 to 30% by weight, and the amount of a monomer (d) may be 3 to 30% by weight, based on 100% by weight of the total of the monomers (a) to (d).
Preferably, the amount of a monomer (a) is 45 to 76% by weight, the amount of the monomer (b) is 5 to 25% by weight, the amount of the monomer (c) is 3 to 30% by weight, and the amount of the monomer (d) is 6 to 25% by weight, in view of high water- and oil-repellency and high water solubility. More preferably, the amount of the monomer (d) is 7 to 15% by weight.
In the present invention, the molecular weight of the fluorine-containing polymer, in addition to the ingredients of the fluorine-containing polymer, has a large influence on the water- and oil-repellency. The weight-average molecular weight of the fluorine-containing polymer in the present invention is 15,000 or more, preferably 30,000 or more in view of high water- and oil-repellency, and is preferably 2,000,000 or less in a view of permeability into micropores. More preferably, the weight-average molecular weight is 40,000 to 110,000. The weight-average molecular weight of the fluorine-containing polymer is determined by GPC (gel permeation chromatography) (in terms of polystyrene).
The fluorine-containing polymer may consist of the monomers (a) to (d), or may contain another monomer in addition to the monomers (a) to (d).
The fluorine-containing polymer may comprise, in addition to the monomers (a) to (d), repeating units derived from a silicon-containing monomer, but may not comprise the same. The use of the silicon-containing monomer can improve the permeability into and adhesion to the masonry substrate.
The silicon-containing monomer is a monomer having at least one silicon atom and one ethylenically unsaturated double bond (carbon-carbon double bond).
The silicon-containing monomer may be monomer represented by, for example, the formula:
wherein A is a monovalent group having at least one silicon atom, and
R1 is a hydrogen atom or a methyl group.
The A group may be represented by the formula:
Rsi—X—
wherein Rsi is R11—(Si(R12)2)p— or R11—(Si(R12)2—O)p—
where R11 is a hydrogen atom or C1-C8 alkyl group or a C6-C8 aryl group,
each of R12 is, the same or different, a hydrogen atom, or a C1-C8 hydrocarbon group or halogenated hydrocarbon group which may have a functional group, and
p is the number of 1 to 100, and
X is a direct bond, —(CH2)q— where q is a number of 1 to 20, —(CH2)r—O— where r is a number of 0 to 20, or —(CH2)s—OC(═O)— where s is a number of 0 to 20.
The functional group in the A group includes a hydroxyl group, an epoxy group, a chloromethyl group, a blocked isocyanate, an amino group and a carboxyl group. Examples of the C1-C8 hydrocarbon group or C1-C8 halogenated hydrocarbon group which may have a functional group are as follows:
—R3COOH
—R3—SH
—R3—Cl [Chemical Formula 3]
wherein R3 and R4 are a direct bond, or an C1-21 aliphatic group (for example, an alkylene group), aromatic group or araliphatic group.
Specific examples of the silicon-containing monomer include vinyltrimetoxysilane, vinyltriethoxysilane,
The amount of the silicon-containing monomer in the fluorine-containing polymer may be 30% by weight or less, for example, 1 to 20% by weight, based on the fluorine-containing polymer.
The treatment composition of the present invention comprises the fluorine-containing copolymer and an aqueous medium. The term “aqueous medium” used herein means a medium only consisting of water, and a medium comprising, in addition to water, an organic solvent (The amount of the organic solvent is 80 parts by weight or less, for example, 0.1 to 50 parts by weight, particularly 5 to 30 parts by weight, based on 100 parts by weight of water).
The fluorine-containing polymer of the present invention can be produced by any of conventional polymerization methods and the polymerization condition can be optionally selected. The polymerization method includes, for example, a solution polymerization, a suspension polymerization and an emulsion polymerization. The solution polymerization is particularly preferable.
In the solution polymerization, there can be used a method of dissolving the monomer(s) into an organic solvent in the presence of a polymerization initiator, replacing the atmosphere by nitrogen, and stirring the mixture with heating, for example, at the temperature within the range from 50° C. to 120° C. for 1 hour to 10 hours. Examples of the polymerization initiator include azobisisobutyronitrile, azobisisovaleronitrile, benzoyl peroxide, di-tert-butyl peroxide, lauryl peroxide, cumene hydroperoxide, t-butyl peroxypivalate and diisopropyl peroxydicarbonate. The polymerization initiator may be used in the amount within the range from 0.01 to 5 parts by weight based on 100 parts by weight of the monomers.
The organic solvent is inert to the monomer(s) and dissolves the monomer(s), and examples thereof include pentane, hexane, heptane, octane, isooctane, cyclohexane, benzene, toluene, xylene, petroleum ether, a commercial petroleum solvent (for example, EXXSOL D40 and ISOPAR E manufactured by Exxon Mobil Corporation), tetrahydrofuran, 1,4-dioxane, acetone, methyl ethyl ketone, methyl isobutyl ketone, methyl acetate, ethyl acetate, butyl acetate, t-butyl acetate, isopropanol, propylene glycol methyl ether acetate, p-chlorobenzotrifluoride, 1,1,2,2-tetrachloroethane, 1,1,1-trichloroethane, trichloroethylene, perchloroethylene, tetrachlorodifluoroethane and trichlorotrifluoroethane. The organic solvent may be used in the amount within the range from 50 to 1,000 parts by weight, based on 100 parts by weight of total of the monomers.
The aqueous solution or aqueous dispersion of the polymer can be obtained by, after a polymerization reaction, adding water added to a reaction mixture and removing (for example, distilling) the organic solvent (a solvent substitution method).
The treatment composition can be produced also by a method other than the solvent substitution method. The treatment composition may be produced by, for example, adding water after the polymerization.
The production of the treatment composition can be performed by merely polymerizing the monomers in the liquid medium or diluting with an additional liquid medium after the polymerization. The liquid medium for polymerization and the liquid medium for dilution may be the same or different medium. Examples of the liquid medium for polymerization and the liquid medium for dilution may be water alone, water-soluble or water-dispersible organic solvent alone, or a mixture of a water-soluble or water-dispersible organic solvent with water. The monomer and the liquid medium are preferably in a form of a solution wherein the monomer is dissolved in the liquid medium. The polymerization may be a solution polymerization or an emulsion polymerization, preferably a solution polymerization in view of stability of polymerization reaction.
The structural units from the monomer (d) (the anion-donating group) may be neutralized by adding a base (such as an aqueous solution of inorganic or organic base) after carrying out the polymerization; or the polymerization may be carried out by using the monomer (d) neutralized with the base in advance. When the monomers are polymerized after the monomer (d) is neutralized with the base in advance, the neutralization with a basic aqueous solution is not necessary.
Examples of the inorganic or organic bases include sodium hydroxide, potassium hydroxide, ammonia, triethylamine, tri-n-propylamine, triisopropylamine, tri-n-butylamine, tri-sec-butylamine, ethanolamine, diethanolamine, triethanolamine, 2-amino-2-methyl-1-propanol, 2-aminomethyl-1,3-propanediol, 2-amino-2-hydroxymethyl-1,3-propanediol, bis(hydroxymethyl) methylaminomethane, tris(hydroxymethyl) aminomethane, lysine and arginine. Among these bases, for example, sodium hydroxide, potassium hydroxide, ammonia, triethylamine, diethanolamine and triethanolamine are preferable in view of the improvement of the dispersibility of the obtained fluorine-containing polymer in the aqueous medium.
The polymer mixture after polymerization may be, if necessary, diluted by adding the aqueous medium (particularly, water).
Non-limiting examples of the water-soluble or water-dispersible organic solvents which are a liquid medium utilized in polymerization include ketones (for example, acetone or methyl ethyl ketone), alcohols (for example, methanol, ethanol and isopropanol), ethers (for example, methyl or ethyl ether of ethylene glycol or propylene glycol, acetate ester thereof, tetrahydrofuran and dioxane), acetonitrile, dimethylformamide, N-methyl-2-pyrollidone, butyllactone and dimethylsulfoxide. Among them, methyl ethyl ketone (MEK), N-methyl-2-pyrollidone (NMP), a mixture of N-methyl-2-pyrollidone and acetone, isopropanol or methanol is preferably used as a solvent. The total monomer concentration in the solution may be in the range of 20 to 70% by weight, preferably, 40 to 60% by weight.
The polymerization may be carried out by using at least one initiator in the amount of 0.1 to 3.0% by weight based on the total weight of the monomers. Peroxides such as benzoyl peroxide, lauroyl peroxide, succinyl peroxide and tert-butyl perpivalate, or azo-compounds such as 2,2-azobis-isobutylonitrile, 4, 4-azobis (4-cyanopentanoic acid) and azodicarbonamide may be used as the initiator.
A chain transfer agent may be used for controlling the molecular weight of the copolymer. Examples of the chain transfer agent preferably include alkylmercaptan (such as dodecylmercaptan, laurylmercaptan and stearylmercaptan), aminoethanethiol, mercaptoethanol, thioglycollic acid and 2-mercaptopropionic acid. The amount of the chain transfer agent used may be in the range of 0.01 to 2 parts by weight, for example, 0.05 to 1 parts by weight, based on 100 parts by weight of the total monomers in the polymerization reaction.
The polymerization can be carried out in the range from 40° C. to a boiling point of the reaction mixture.
The dilution step may be carried out by adding the liquid medium such as water or an aqueous solution of a strong or moderate inorganic or organic base into the solution of the fluorine-containing polymer in the organic solvent. The above-mentioned examples of the bases are the same as the above-mentioned bases. Among them, sodium hydroxide and/or ammonia are preferably used. The amount of the aqueous solution and the concentration of the base are preferable to be sufficiently enough to neutralize the carboxylic acid group or the sulfonic acid group of the monomer (d) and also to give a solid content of a final fluorine-containing polymer solution of 5 to 35% by weight, preferably 15 to 25% by weight.
In order to neutralize the carboxylic acid group and the sulfonic acid group, it is advantageous to use the amount of base in the range of 0.1 to 5 eq., preferably 0.5 to 3 eq., based on the monomer (d).
In the present invention, the treatment agent (such as the water- and oil-repellent agent or the soil resistant agent) comprises (1) the fluorine-containing polymer, and (2) the liquid medium, that is, water or the mixture of water and the water-soluble organic solvent. Examples of the water-soluble organic solvent include alcohols such as methanol, ethanol, n-propanol and isopropanol; and ketones such as acetone. The amount of the water-soluble organic solvent may be 50% by weight or less, for example, 1 to 30% by weight, based on the mixture (total of water and the water-soluble organic solvent).
Preferably, the treatment agent is in the form of a solution (for example, an aqueous solution) of the fluorine-containing polymer.
In the treatment agent, the amount of the fluorine-containing polymer is not limited, and said amount may be suitably selected from the limited range giving a homogeneous solution. The amount of the fluorine-containing polymer may be 0.1 to 50% by weight, for example, 0.2 to 20% by weight, particularly 0.5 to 10% by weight, based on the treatment agent.
The treatment agent of the present invention may contain (3) an additive, in addition to (1) the fluorine-containing polymer and (2) the liquid medium.
Examples of the additive (3) include a silicon-containing compound, a wax and an acrylic emulsion.
The treatment agent may contain, in addition to above-mentioned components (1) to (3), if needed, another water repellent agent, another oil repellent agent, a rate-of-drying regulator, a cross linking agent, a film formation assistant, a compatibilizer, a surface active agent, an antifreezing agent, a viscosity controlling agent, an ultraviolet ray absorbent, an antioxidant, a pH adjuster, a defoaming agent, an aesthetic property regulator, a slide regulator, an antistatic agent, a hydrophilization agent, antibacterial medicine, antiseptics, an insecticide, an aromatic agent and a flame retardant.
In the present invention, the treatment agent is applied to the substrate to give the water- and oil-repellency and the soil resistance to the substrate.
The substrate is masonry such as a stone. Examples of the masonry include a stone, a brick, a concrete and a tile. Examples of the stone include a natural stone (for example, marble and granite) and an artificial stone.
The masonry is treated by applying (coating) the treatment agent to the substrate. The amount of the treatment agent may be such that the fluorine-containing polymer contained in the treatment agent is 0.05 to 50 g/m2, for example, 0.1 to 20 g/m2, preferably 1 to 10 g/m2. The coating may be conducted once or a plurality of times. The coating method may be any of, for example, brushing, spraying, rolling, dipping and use of a waste cloth containing the treatment agent. The excess of the treatment agent may be wiped off according to the necessity. Then the treatment agent is dried to remove the liquid medium. The drying may be conducted at room temperature (20° C.), and/or the baking may be conducted at 80° C. to 250° C.
The “treatment” means that a treatment agent is applied to a substrate by, for example, dipping, spraying or coating. The treatment gives the result that the fluorine-containing polymer which is an active component of the treatment agent is adhered to surfaces of the substrate and/or penetrated into internal parts of the substrate.
The present invention is specifically illustrated by showing Examples and Comparative Examples which are merely specific examples of the present invention and which do not limit the present invention. Hereinafter, the terms “parts” and “%” mean “parts by weight (or pbw)” and “% by weight (or wt %)”, respectively, if not specified.
The testing methods used herein are as follows:
A weight-average molecular weight of the fluorine-containing copolymer is determined by GPC (gel permeation chromatography) (in terms of polystyrene).
Dispersion stability of the fluorine-containing copolymer was observed. An aqueous dispersion having a solid concentration of 20% by weight was prepared and put into a glass sample bottle, the bottle was stood at room temperature for seven days and then the existence of sedimentation or aggregation was visually observed. The evaluation criterion was as follows:
Good: No sedimentation and aggregation,
Fair: Slight sedimentation and aggregation, and
Bad: Much sedimentation and aggregation.
An aqueous soil (for example, red wine and coffee) was dropped on the treated substrate, the drop was allowed to stand for 24 hours, and the soil was removed by lightly water-wiping with a paper towel. Visual evaluation was performed in accordance with the following criterion.
0: Deep stain, large spread of stain
1: Deep stain, slight or no spread of stain
2: Moderate stain, no spread of stain
3: Slight stain
4: No stain
An oily soil (for example, olive oil and red chili pepper oil) was put on the treated substrate, the drop was allowed to stand for 24 hours, and the soil was removed by lightly water-wiping with a paper towel. Visual evaluation was performed in accordance with the following criterion.
0: Deep stain, large spread of stain
1: Deep stain, slight or no spread of stain
2: Moderate stain, no spread of stain
3: Slight stain
4: No stain
53.70 g of CF3CF2—(CF2CF2)2—CH2CH2OCOC(CH3)═CH2 (C6SFMA), 17.90 g of hydroxyethyl methacrylate (HEMA), 8.95 g of ω-hydroxy-polyoxyethylene acrylate (HPOEA) (average polymerization degree of polyoxyethylene group≈6), 8.95 g of methacrylic acid and 395.70 g of the methyl ethyl ketone were stirred and dissolved in a four-necked flask, and kept at 64° C. with purging with a nitrogen gas. 1.13 g of t-butyl peroxypivalate was added to react at 64° C. for 8 hours to give a solution of a polymer. A conversion of the monomers determined with a gas chromatography was 90% or more. A weight-average molecular weight of the produced polymer was 80,000.
The same procedure as in Synthesis Example 1 was repeated except changing the amount of CF3CF2—(CF2CF2)2—CH2CH2OCOC(CH3)═CH2 (C6SFMA) into 52.81 g and the amount of methacrylic acid into 9.85 g. A conversion of the monomers determined with a gas chromatography was 90% or more.
The same procedure as in Synthesis Example 1 was repeated except changing the amount of CF3CF2—(CF2CF2)2—CH2CH2OCOC(CH3)═CH2 (C6SFMA) into 54.60 g and the amount of methacrylic acid into 8.06 g. A conversion of the monomers determined with a gas chromatography was 90% or more.
The same procedure as in Synthesis Example 1 was repeated except adding 1.79 g of lauryl mercaptan (L-SH) as a chain transfer agent. A conversion of the monomers determined with a gas chromatography was 90% or more.
The same procedure as in Synthesis Example 1 was repeated except adding 2.69 g of lauryl mercaptan (L-SH) as a chain transfer agent. A conversion of the monomers determined with a gas chromatography was 90% or more.
The same procedure as in Synthesis Example 1 was repeated except that 54.60 g of CF3CF2—(CF2CF2)2—CH2CH2OCOCH═CH2 (C6SFA) was used instead of C6SFMA and the amount of methacrylic acid was changed into 8.06 g. A conversion of the monomers determined with a gas chromatography was 90% or more.
The same procedure as in Synthesis Example 1 was repeated except that the amount of methacrylic acid was changed into 4.48 g and 4.48 g of itaconic acid was added. A conversion of the monomers determined with a gas chromatography was 90% or more.
The same procedure as in Synthesis Example 1 was repeated except changing the amount of CF3CF2—(CF2CF2)2—CH2CH2OCOC(CH3)═CH2 (C6SFMA) into 62.65 g and the amount of methacrylic acid into 0 g. A conversion of the monomers determined with a gas chromatography was 90% or more.
The same procedure as in Synthesis Example 1 was repeated except changing the amount of CF3CF2—(CF2CF2)2—CH2CH2OCOC(CH3)═CH2 (C6SFMA) into 71.60 g and the amount of hydroxyethyl methacrylate (HEMA) into 0 g. A conversion of the monomers determined with a gas chromatography was 90% or more.
The same procedure as in Synthesis Example 1 was repeated except changing the amount of CF3CF2—(CF2CF2)2—CH2CH2OCOC(CH3)═CH2 (C6SFMA) into 62.65 g and the amount of ω-hydroxy-polyoxyethylene acrylate (HPOEA) into 0 g. A conversion of the monomers determined with a gas chromatography was 90% or more.
The ingredients and the weight-average molecular weights of the polymers which were obtained by Synthesis Examples and Comparative Synthesis Examples are shown in Table 1.
A transparent pale-yellow aqueous dispersion was obtained by adding 48.48 g of 1.0% of an aqueous sodium hydroxide solutions as a base to 35 g of the fluorine-containing copolymer solution obtained by Synthesis Example 1, and distilling off methyl ethyl ketone with heating under a reduced pressure with an evaporator. Ion exchanged water was further added to this aqueous dispersion to obtain an aqueous dispersion having a solid content of 20% by weight. The results of evaluating the dispersion stability of the obtained aqueous dispersion are shown in Table 1.
The same procedure as in Preparation Example 1 was repeated except adding 54.35 g of 1.0% of an aqueous sodium hydroxide solution as a base to 35 g of the fluorine-containing copolymer solution obtained in Synthesis Example 2.
The same procedure as in Preparation Example 1 was repeated except adding 41.87 g of 1.0% of an aqueous sodium hydroxide solution as a base to 35 g of the fluorine-containing copolymer solution obtained in Synthesis Example 3.
The same procedure as in Preparation Example 1 was repeated except adding 48.48 g of 1.0% of an aqueous sodium hydroxide solution as a base to 35 g of the fluorine-containing copolymer solution obtained in Synthesis Example 4.
The same procedure as in Preparation Example 1 was repeated except adding 48.48 g of 1.0% of an aqueous sodium hydroxide solution as a base to 35 g of the fluorine-containing copolymer solution obtained in Synthesis Example 5.
The same procedure as in Preparation Example 1 was repeated except adding 41.87 g of 1.0% of an aqueous sodium hydroxide solution as a base to 35 g of the fluorine-containing copolymer solution obtained in Synthesis Example 6.
The same procedure as in Preparation Example 1 was repeated except adding 57.36 g of 2.1% of an aqueous sodium hydroxide solution as a base to 35 g of the fluorine-containing copolymer solution obtained in Synthesis Example 7.
The same procedure as in Preparation Example 1 was repeated except adding 48.48 g of ion exchanged water to 35 g of the polymer solution obtained in Comparative Synthesis Example 1.
The same procedure as in Preparation Example 1 was repeated except adding 48.48 g of 1.0% of an aqueous sodium hydroxide solution as a base to 35 g of the fluorine-containing copolymer solution obtained in Comparative Synthesis Example 2.
The same procedure as in Preparation Example 1 was repeated except adding 48.48 g of 1.0% of an aqueous sodium hydroxide solution as a base to 35 g of the fluorine-containing copolymer solution obtained in Comparative Synthesis Example 3.
The aqueous dispersion obtained by Preparation Example 1 was diluted with ion exchanged water to give a solid content of 3% by weight. The treatment liquid was applied to a surface of a polished porous base material (1 g of the treatment liquid, per area of 5 cm×10 cm), and an excess of the treatment liquid was wiped off after leaving in 10 minutes at room temperature. The soil resistance test (water repellency and oil repellency) was conducted after further leaving at room temperature for 24 hours.
Limestone (Moka Cream, water-polished) and granite (China White, jet bumer-treated) were used as the porous base material.
The results are shown in Table 1.
The same procedure as in Example 1 was repeated except using the aqueous dispersions obtained by Preparation Examples 2 to 7.
The aqueous dispersion obtained by Comparative Preparation Example 1 was used.
The aqueous dispersion obtained by Comparative Preparation Example 2 was used.
The same procedure as in Example 1 was repeated except using the aqueous dispersion obtained by Comparative Preparation Example 3.
The masonry treatment composition of the present invention can treat various masonries by a simple spreading operation, without causing the problem of a volatile organic compound (VOC).
| Number | Date | Country | Kind |
|---|---|---|---|
| 2014-109973 | May 2014 | JP | national |
This application is a Rule 53(b) Divisional Application of U.S. application Ser. No. 15/313,594, filed on Nov. 23, 2016, which is a National Stage of International Application No. PCT/JP2015/064587, filed on May 21, 2015, which claims priority from Japanese Patent Application No. 2014-109973, filed on May 28, 2014, the contents of all of which are incorporated herein by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15313594 | Nov 2016 | US |
| Child | 16528425 | US |
