[Technical Field]
[0001] The present invention relates to a water- and oil-repellent. More specifically, the
present invention relates to a water- and oil-repellent of which washing resistance
is improved.
[Background Art]
[0002] The expression of water- and oil-repellency results from the low surface energy of
fluorine, and, usually, fluorine-containing acrylate polymers are widely used as active
ingredients of water- and oil-repellents. Previous various investigations have shown
that the presence of crystallinity in a fluorine-containing polymer is necessary for
expressing water- and oil-repellency in practical applications. In particular, it
has been recognized that the hydrophobicity of a fluorine-containing polymer depends
on the number of carbon atoms of a side-chain fluoroalkyl group and that the expression
of crystallinity is observed when the number of carbon atoms is eight or more.
[Non-Patent Document 1]
Secchaku (Adhesion), Vol. 50, No. 5, pp. 16-22 (2006)
[0003] Therefore, it has been regarded that a fluorine-containing polymer having a short
fluoroalkyl group, i.e., a side-chain fluoroalkyl group having 7 or less, in particular,
6 or less carbon atoms, is low in or does not have crystallinity and thereby cannot
provide water-repellent performance that is sufficient for practical use. In addition,
since water- and oil-repellents are required to have washing resistance and abrasion
resistance, fluorine-containing acrylic polymers having long side chains are used.
[0004] However, polymers including a side-chain fluoroalkyl group having 8 or more carbon
atoms are very hard due to their high crystallinity and have a problem that flexibility
of textile products is impaired. Furthermore, since the water-repellent process needs
high curing temperature, there are problems such as a change in color of fibers. In
addition, since a long side-chain having 8 or more carbon atoms is excessively hydrophobic,
a large amount of an emulsifier is necessary for producing a water- and oil-repellent.
[0005] The present applicant has before proposed a water- and oil-repellent composed of
an aqueous emulsion in which a copolymer of a fluoroalkyl group-containing polymerizable
monomer and vinylidene chloride or benzyl (meth)acrylate, and a carboxyl group-containing
water-soluble polymer are dispersed in water using a nonionic surfactant. The fluoroalkyl
group of a fluoroalkyl group-containing polymerizable monomer that is copolymerized
with vinylidene chloride or benzyl (meth)acrylate is recognized to be a perfluoroalkyl
group having 4 to 20 carbon atoms, but the perfluoroalkyl group used in the above-mentioned
polymerization example is recognized to be a mixture of perfluoroalkyl groups having
6 to 14 carbon atoms, 9.0 on average.
[Patent Document 1]
JP-A-11-80710
[0006] Furthermore, as a water-dispersible water- and oil-repellent composition in which
both the repeated washing resistance and the water pressure resistance of water- and
oil-repellency are achieved, a water-dispersible water- and oil-repellent composition
including as active ingredients (A) a fluorine-containing copolymer having a hydroxyl
group, (B) a fluorine-containing copolymer having an epoxy group, (C) a compound having
a blocked isocyanate group and not having a carbon-carbon unsaturated bond, and (D)
an amino resin has been proposed. The fluorine-containing copolymers having the hydroxyl
group or the epoxy group are each a copolymer of a polymerizable monomer having a
polyfluoroalkyl group, wherein the number of carbon atoms of the perfluoroalkyl group
of a perfluoroalkylalkyl group is 2 to 20, preferably 6 to 16. A perfluoropentyl group
and a perfluorohexyl group are shown as examples, and in the Examples, a mixture of
F(CF
2)
m groups of which m is from 6 to 16 and is 9 on average is used.
[Patent Document 2]
WO 00/58416
[0007] Accordingly, it is believed that a water- and oil-repellent showing excellent in
flexibility and also excellent in washing resistance can be obtained if water- and
oil-repellency can be expressed with a fluorine-containing polymer including a short
fluoroalkyl group having 6 or less carbon atoms.
[0008] Furthermore, acrylic acid derivatives of perfluoroalkylalkyl alcohol, for example,
CF
3(CF
2)
7CH
2CH
2OCOCH=CH
2, are widely used as synthetic monomers for fluorine-containing copolymer that forms
a water- and oil-repellent for fiber, but recently, it has been reported that among
these types of compounds, compounds including perfluoroalkyl groups having approximately
8 carbon atoms are high in bioaccumulation potential and therefore have an environmental
problem. Accordingly, it is concerned that the manufacturing and the use of these
compounds will become difficult in the future. However, compounds including perfluoroalkyl
groups having 6 or less carbon atoms are recognized to be low in bioaccumulation potential.
[0009] It has been also proposed a surface-treating agent showing excellent water repellency,
oil repellency, and antifouling property by using a polymer having a short fluoroalkyl
group having 1 to 6 carbon atoms as the side chain, but the fluoroalkyl group-containing
monomer used therein is a fluorine-containing monomer compound represented by the
general formula:
Rf-Y-O-CO-CX=CH
2
X: F, Cl, Br, I, CFX1X2, CN, a fluoroalkyl group having 1 to 20 carbon atoms, benzyl group, or phenyl group,
Y: an aliphatic group having 1 to 10 carbon atoms, an aromatic or alicyclic group
having 6 to 10 carbon atoms, a CH2CH2NR1SO2 group, or a CH2CH(OY1)CH2 group, and
Rf: a fluoroalkyl group having 1 to 6 carbon atoms.
Acrylic acid derivatives in which X is H are shown as comparative manufacturing examples,
and methacrylic acid derivatives in which X is CH
3 are intendedly excluded.
[Patent Document 3]
JP-A-2004-352976
[0010] Furthermore, it has been proposed a water- and oil-repellent composition of which
essential component is a copolymer containing as a polymerization unit (a) an Rf group-containing
monomer of which homopolymer does not have a melting point derived from the Rf group
in the microcrystals or has a melting point of 55°C or less and has a glass transition
point of 20°C or more and (b) an Rf group-free monomer having a cross-linkable functional
group, wherein the composition can impart excellent water- and oil-repellency to products,
even in low temperature treatment, and also can perform a water- and oil-repellent
process with providing soft textile feeling and also excellent durability.
[Patent Document 4]
WO 2004/035708
[0011] In the above, a perfluoroalkylalkyl (meth)acrylate is used as the component monomer
(a), but a specific monomer, such as a 2-butanone oxime adduct, pyrazole adduct, or
ε-caprolactam adduct of a ω-isocyanate alkyl(meth)acrylate, is used as the component
monomer (b) in the copolymerization reaction.
[0012] Furthermore, the use of water- and oil-repellency processing treatment is extended
to the outdoor field such as sportswear, and the water- and oil-repellency is required
to be durable to repeated washing in such an application field. However, though the
above-mentioned Patent Document 2 describes the water-dispersible water- and oil-repellent
composition as that in which both the repeated washing resistance and the water resistance
of water- and oil-repellency are achieved, a fluorine-containing copolymer including
a perfluoroalkyl group having 6 or less carbon atom is not substantially used alone,
and also the water-dispersible water- and oil-repellent composition can not impart
sufficient water- and oil-repellency not only to synthetic fibers but also to natural
fibers when it is used for water- and oil-repellency treatment.
[Disclosure of the Invention]
[Problems to be Solved by the Invention]
[0013] It is an object of the present invention to provide a water- and oil-repellent that
includes, as an active ingredient, a copolymer of a perfluoroalkylalkyl (meth)acrylate
being low in bioaccumulation potential, and can impart sufficient water- and oil-repellency
not only to synthetic fibers but also to natural fibers, and is also improved in washing
resistance.
[Means for Solving the Problems]
[0014] Such an object of the preset invention is achieved by a water- and oil-repellent
comprising an aqueous dispersion of a fluorine-containing copolymer including as a
copolymerization unit
- (a) at least one of perfluoroalkylalkyl acrylates and corresponding methacrylates
represented by the general formula:
CnF2n+1CmH2m OCOCR=CH2
(wherein R represents hydrogen atom or methyl group; n represents 4, 5, or 6; and
m represents 1, 2, 3, or 4),
- (b) benzyl acrylate or benzyl methacrylate,
- (c) vinylidene chloride and
- (d) a cross-linkable group-containing polymerizable monomer;
and
a blocked isocyanate added to the aqueous dispersion in a weight ratio of 0.05 to
3.0 to the weight of the solid content of the aqueous dispersion.
[Effect of the Invention]
[0015] The water- and oil-repellent according to the present invention is a water- and oil-repellent
of which an active ingredient is a copolymer of a perfluoroalkylalkyl (meth)acrylate
being low in bioaccumulation potential, wherein the copolymer is not that in which
a specific monomer is copolymerized; the curing temperature in water- and oil-repellent
treatment using the copolymer as an active ingredient is low; and excellent textile
feeling can be imparted to a water- and oil-repellent-treated fabric. In particular,
the water- and oil-repellent can impart sufficient water- and oil-repellency not only
to synthetic fibers but also to natural fibers, and is also excellent in washing resistance.
[Best Mode for Carrying Out the Invention]
[0016] Preferred examples of the component (a), perfluoroalkylalkyl (meth)acrylate, represented
by the general formula:
C
nF
2n+1C
mH
2mOCOCR=CH
2
R: a hydrogen atom or a methyl group
n: 4, 5, or 6
m: 1, 2, 3, or 4
include the following compounds:
C
4F
9CH
2CH
2OCOCH=CH
2,
C
4F
9CH
2CH
2OCOC(CH
3)=CH
2,
C
6F
13CH
2CH
2OCOCH=CH
2,
and
C
6F
13CH
2CH
2OCOC(CH
3)=CH
2.
[0017] The component (a), perfluoroalkylalkyl (meth)acrylate, is supplied to a copolymerization
reaction in such a ratio that its proportion in the resulting copolymer is about 10
to 80% by weight, preferably about 25 to 80% by weight, and more preferably about
40 to 80% by weight. By the copolymerization of such a monomer component (a), an aqueous
dispersion showing excellent in emulsion stability can be formed, and water- and oil-repellency
is expressed.
[0018] The component (b), benzyl acrylate or benzyl methacrylate, is supplied to the copolymerization
reaction in such a ratio that its proportion in the resulting copolymer is about 5
to 80% by weight, preferably about 5 to 50% by weight, and more preferably about 5
to 35% by weight. By the copolymerization of the benzyl (meth)acrylate, the copolymer
shows a good film-forming property and orientation.
[0019] As the component (c), vinylidene chlorides is used.
[0020] The fluorine-free polymerizable monomer other than benzyl (meth)acrylates is supplied
to the copolymerization reaction in such a ratio that its proportion in the resulting
copolymer is about 5 to 80% by weight, preferably about 5 to 60% by weight, and more
preferably about 5 to 40% by weight.
[0021] Examples of the component (d), cross-linkable group-containing polymerizable monomer,
include epoxy group-containing monomers such as allyl glycidyl ether and glycidyl
(meth)acrylate; N-methylol group-containing monomers such as N-methylol (meth)acrylamide
and N-butoxymethylol (meth)acrylamide; hydroxyalkyl group-containing monomers such
as 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl acrylate, 4-hydroxybutyl acrylate,
and 2-hydroxy-3-chloropropyl (meth)acrylate; amide group-containing monomers such
as (meth)acrylamide, N-methyl acrylamide, diacetone acrylamide; and compounds represented
by the formula:
CH
2=C(CH
3)CON
--N
+(CH3)
2CH
2CH(OH)CH
3,
or
CH
2=C(CH
3)CON
--N
+(CH
3)
3;
aziridinyl group-containing monomers such as aziridinylethyl (meth)acrylate; and polyol
poly(meth)acrylates such as ethylene glycol di(meth)acrylate, polyoxyethylene di(meth)acrylate,
and polyoxypropylene glycol di(meth)acrylate. Hydrophilic monomers are preferably
used.
[0022] Further copolymerization of the cross-linkable group-containing polymerizable monomer
strengthens the adhesion, to base materials such as fibers, of the fluorine-containing
copolymer used as an active component for water- and oil-repellency; also shows an
effect of improving, for example, the durability, washing resistance, and dry-cleaning
resistance of the water- and oil-repellent; and also usually gives a secondary effect
of improving the polymerization stability during emulsion polymerization. Therefore,
the component (d) is used in such a ratio that its proportion in the copolymer is
about 0.5 to 40% by weight and preferably about 1 to 15% by weight.
[0023] The copolymerization reaction using these polymerizable monomers is performed by
emulsion polymerization in the presence of a surface-active emulsifier composed of
a polyethylene oxide adduct type cationic surfactant or of both said cationic surfactant
and a polyethylene oxide adduct type nonionic surfactant and in the presence of an
emulsifying aid composed of a glycol-based compound. The ratio of the surface-active
emulsifier is about 1 to 20% by weight and preferably about 1 to 10% by weight, and
the ratio of the emulsifying aid is about 10 to 100% by weight and preferably about
15 to 70% by weight, based on the total amount of the monomers for the copolymerization.
[0024] As such a cationic surfactant, a polyethylene oxide adduct of a quaternary ammonium-based
surfactant, for example, an alkylammonium chloride or alkylpyridinium salt having
1 to 3 polyoxyethylene groups, is used. On this occasion, a cationic surfactant without
the polyethylene oxide, for example, a quaternary ammonium-based surfactant, can be
simultaneously used. In such a case, the weight ratio is preferably about 0.1 to 2
to the polyethylene oxide adduct type.
[0025] In addition, as the polyethylene oxide adduct type nonionic surfactant simultaneously
used with the cationic surfactant, for example, a reaction product of a polyethylene
oxide with an alcohol such as an aliphatic alcohol or an aromatic alcohol, an alkyl
ether, oleic acid, a C
12 to C
18 alkylamine, or sorbitan mono fatty acid is used in a ratio of about 80% by weight
or less and preferably about 30 to 80% by weight in the total amount with the polyethylene
oxide adduct type cationic surfactant.
[0026] Here, instead of the cationic surfactant, those in which an amine compound having
a polyethylene oxide chain, for example, a polyoxyethylene octadecylamine (such as
Amiet-320, a Kao product), a polyoxyethylene alkyldiamine (such as Esoduomin T/25,
a Lion product) represented by the general formula:
H(OCH
2CH
2)
xNRCH
2CH
2CH
2N[(CH
2CH
2O)
yH](CH
2CH
2O)
zH,
or a polyoxyethylene dodecylamine (such as Nymeen L-207, a NOF product) is neutralized
with an organic acid such as acetic acid can be used.
[0027] Examples of the glycol compound as the emulsifying aid used in a combination with
the emulsifier include ethylene glycol, polyethylene (n=2 to 4 or more) glycol, propylene
glycol, polypropylene (n=2 to 4 or more) glycol, their terminal monomethyl ethers,
hexylene glycol, and propylene glycol adducts of glycerin. A polypropylene glycol-based
compound having a molecular weight of about 300 to 3000 or hexylene glycol is preferably
used.
[0028] Prior to the copolymerization reaction, a polymerizable monomer mixture containing
a perfluoroalkylalkyl (meth)acrylate and another polymerizable monomer is subjected
to emulsification treatment in the presence of a surface-active emulsifier and an
emulsifying aid. The emulsification treatment is sufficiently carried out using a
high-pressure homogenizer or the like.
[0029] The copolymerization reaction of the emulsified polymerizable monomer mixture is
performed in the presence of a radical polymerization initiator added to the reaction
system. The radical polymerization initiator may be any of organic peroxides, azo
compounds, and persulfates. Preferably, a water-soluble organic peroxide, for example,
2,2'-azobis(2-amidinopropane)·dihydrochloride, is used in a ratio of about 0.1 to
10% by weight and preferably about 0.5 to 7% by weight to the total weight of the
polymerizable monomer mixture.
[0030] The copolymerization reaction is carried out in an aqueous solvent at about 40 to
80°C for about 1 to 10 hours to form an aqueous dispersion (aqueous emulsion) serving
as a stock solution having a solid content concentration of about 15 to 35% by weight.
As the aqueous solvent, in addition to the use of water alone, preferably used an
aqueous solvents containing about 1 to 30% by weight of a water-soluble organic solvent,
for example, a ketone such as acetone or methyl ethyl ketone, an alcohol such as methanol
or ethanol, or a glycol such as ethylene glycol, propylene glycol, dipropylene glycol,
a monomethyl ether thereof, or a tripropylene glycol. In the reaction, a molecular
weight modifier may be used, and, for example, an alkyl mercaptan such as n-octyl
mercaptan, n-dodecyl mercaptan, or tertiary dodecyl mercaptan is preferably used.
[0031] To the resulting aqueous dispersion (aqueous emulsion), a blocked isocyanate is added
as an cross-linking agent in a weight ratio of 0.05 to 3.0, preferably 0.2 to 2.0,
to the weight of solid content of the aqueous dispersion. The blocked isocyanate can
impart excellent water-repellency and high washing resistance to also natural fibers
such as cotton. When the amount of the blocked isocyanate is lower than the above-mentioned
ratio, the washing resistance is decreased. On the other hand, when the blocked isocyanate
is used in an amount higher than the ratio, the textile feeling of a fabric is deteriorated.
[Patent Document 5]
WO 2005/118737
[0032] The blocked isocyanate herein is a compound having one or more blocked isocyanate
group and not having a polymerizable carbon-carbon unsaturated bond, i.e., a compound
having a structure in which the isocyanate group is blocked with a blocking agent.
As such a blocked isocyanate, a preferred structure is obtained by reacting a polyisocyanate
and a compound having two or more active hydrogen atoms in a molecule thereof and
blocking the isocyanate group of the resulting compound with a blocking agent.
[0033] Examples of the polyisocyanate include aromatic isocyanates such as 4,4'-diphenylmethane
diisocyanate, 2,4'-diphenylmethane diisocyanate, and tolylene diisocyanate; aliphatic
isocyanates such as trimethylene diisocyanate, tetramethylene diisocyanate, pentamethylene
diisocyanate, hexamethylene diisocyanate, 1,2-propane diisocyanate, 1,2-butane diisocyanate,
trimethylhexamethylene diisocyanate, isophorone diisocyanate, 4,4'-dicyclohexylmethane
diisocyanate, and cyclohexylene diisocyanate; and their isocyanurate modified compounds,
prepolymer modified compounds, biuret modified compounds, and allophanate modified
compounds.
[0034] The compound having two or more active hydrogen atoms in the molecule is preferably
a polyol or a polyamine. Examples of the polyol include ethylene glycol, propylene
glycol, butanediols, pentanediols, hexanediols, glycerin, trimethylolpropane, pentaerythritol,
sorbitol, neopentyl glycol, bisphenol A, xylylene glycol, and at least one of modified
compounds of these alcohols. Examples of the polyamine include hexamethylenediamine
and 3,3'-iminobispropylamine. The polyol herein may be a polyester polyol, and as
the polyester polyol, those having an ester bond obtained by a reaction of a polyol
and a polyvalent carboxylic acid such as phthalic acid, adipic acid, fumaric acid,
pyromellitic acid, trimellitic acid, aliphatic dicarboxylic acid, or a derivative
thereof are used.
[0035] As the blocking agent for the isocyanate, alkyl ketone oximes, phenols, alcohols,
β-diketones, and lactams are used, and preferably, methyl ethyl ketone oxime, ε-caprolactam,
phenol, cresol, acetylacetone, diethyl malonate, isopropyl alcohol, tert-butyl alcohol,
and maleic acid imide, more preferably compounds having a dissociation temperature
of from 120 to 180°C represented by dialkyl ketone oximes such as methyl ethyl ketone
oxime and lactams such as ε-caprolactam are used.
[0036] The blocked isocyanate is obtained by, as described above, reacting a polyol to an
isocyanate compound and then reacting the resulting compound to a blocking agent.
These reactions are preferably performed in a non-aqueous solvent such as ketones,
ethers, or hydrocarbons. In addition, it is preferable that the equivalent weights
of the isocyanate compound, the compound having two or more active hydrogen atoms,
and the blocking agent become equal to one another at the time of completion of all
the reactions.
[0037] After the above-described blocking reaction, the blocked isocyanate is preferably
emulsified with water and a nonionic emulsifier, a nonionic/cationic emulsifier, or
a nonionic/anionic emulsifier, in particular, a nonionic/cationic emulsifier. The
solvent is removed after the emulsification, according to need.
[0038] As the blocked isocyanate, commercially available products, for example, RucoGuard
XTS, a Rudolf product; RucoGuard WEB, a Rudolf product; NK Assist-NY, a Nikka Chemical
product; NK Assist-V, a Nikka Chemical product; NK Assist-FU, a Nikka Chemical product;
Prominate XC-830, a Gantsu Chemical product; Prominate XC-915, a Gantsu Chemical product;
Prominate XC-950, a Gantsu Chemical product; and Elastron BN-69, a Daiichi Kogyo Seiyaku
product can be used as such.
[0039] The aqueous dispersion can further contain other additives indispensable for the
water- and oil-repellent use, for example, a cross-linking agent other than the blocked
isocyanate, such as a melamine resin or a urea resin, a polymer extender, another
water-repellent such as a silicone resin or oil, or wax, an insecticide, an antistatic
agent, a dye stabilizer, an anticreasing agent, and a stain blocker.
[0040] The thus obtained aqueous dispersion containing the block isocyanate is diluted with
water, preferably with ion-exchanged water to give a solid content concentration of
about 0.1 to 10% by weight, and then is effectively applied, as a water- and oil-repellent,
to, for example, fibers, a fabric, a woven fabric, paper, a film, a carpet, or a fabric
product made of filaments, threads, or fibers. The application is performed by coating,
dipping, spraying, padding, roll coating, or a combination thereof. For example, a
bath containing a solid content in a concentration of about 0.1 to 10% by weight is
used as a pad bath. A material to be treated is padded in this pad bath and is then
subjected to removal of excessive liquid with a squeezing roller, followed by drying,
thereby allowing the fluorine-containing copolymer to adhere to the material to be
treated in a ratio of about 0.01 to 10% by weight to the amount of the material. Subsequently,
drying, which varies depending on the type of the material to be treated, is usually
conducted at about 100 to 120°C for about from 1 minute to 2 hours to complete the
water- and oil-repellent treatment.
[Examples]
[0041] Next, the present invention will be described with reference to Examples. Note that
percentage in parentheses means % by weight.
Reference Example 1
[0042]
| 2-(n-Perfluorohexyl)ethyl methacrylate |
58.3 g (45.6%) |
| Benzyl methacrylate |
29.2 g (22.8%) |
| 2-Hydroxyethyl methacrylate |
5.6 g ( 4.4%) |
| Polyethylene glycol (n=4) monomethacrylate (PE-200, a NOF product) |
11.7 g ( 9.1%) |
| Lauryl mercaptan (chain transfer agent) |
0.5 g |
| Polyoxyethylene polycyclic phenyl ether (surfactant) |
7.0 g |
| (Newcol-740, a Nippon Nyukazai product) |
|
| Hexylene glycol (emulsifying aid) |
35.0 g |
| Ion-exchanged water |
267.1 g |
[0043] The above-mentioned components were put in a 1-L glass reaction vessel and were mixed,
and further subjected to emulsification mixing using a high-pressure homogenizer.
The resulting emulsion was substituted by nitrogen gas for 30 minutes. Then, the inner
temperature of the reaction vessel was gradually increased to 40°C, and then
| vinylidene chloride |
17.5 g (13.7%) |
| N-methylol acrylamide (dissolved in 29.3 g of ion-exchanged water) |
5.6 g ( 4.4%) |
| 2,2'-azobis(2-amidinopropane)-dihydrochloride |
2.8 g |
| (dissolved in 30.4 g of ion-exchanged water) |
|
were added thereto (the total amount including 285.5 g of total ion-exchanged water
was 500.0 g). Furthermore, the inner temperature was gradually increased to 70°C,
followed by the reaction at the temperature for 4 hours. After the completion of the
reaction and cooling, an aqueous dispersion having a solid content concentration of
25.0% by weight was obtained. The melting point (DSC method) of the copolymer separated
from the aqueous dispersion was 45°C.
Reference Examples 2 to 4
[0044] In Reference Example 1, aqueous dispersions B to D each having a solid content concentration
of 25.0% by weight (excluding Reference Example 2 in which the concentration is 25.3%
by weight) were prepared by changing the kinds and the amounts of the comonomers (a)
to (d) and the total amount of ion-exchanged water to those shown in Table 1. In Table
1, the melting points (DSC method) of the copolymers that are obtained by separating
them from the aqueous dispersions are also shown.
Table 1
| |
|
Reference |
Reference |
Reference |
| |
|
Example 2 |
Example 3 |
Example 4 |
| Comonomer |
g |
% |
g |
% |
g |
% |
| Component (a) |
|
|
|
|
|
|
| |
FAMAC-6 |
78.5 |
61.5 |
100.6 |
79.1 |
62.8 |
49.2 |
| |
FAAC-6 |
|
|
|
|
15.7 |
12.3 |
| Component (b) |
|
|
|
|
|
|
| |
BzMA |
22.4 |
17.6 |
7.4 |
5.8 |
22.4 |
17.6 |
| Component (c) |
|
|
|
|
|
|
| |
PEGM |
4.2 |
3.3 |
4.2 |
3.3 |
4.2 |
3.3 |
| |
VDC |
11.2 |
8.8 |
3.8 |
3.0 |
11.2 |
8.8 |
| Component (d) |
|
|
|
|
|
|
| |
HEA |
5.6 |
4.4 |
5.6 |
4.4 |
5.6 |
4.4 |
| |
NMAM |
5.6 |
4.4 |
|
|
5.6 |
4.4 |
| |
NMMA |
|
|
5.6 |
4.4 |
|
|
| Total amount of water (g) |
323.5 |
|
327.5 |
|
327.2 |
|
| Aqueous dispersion |
B |
|
C |
|
D |
|
| Copolymer melting point |
44 |
|
46 |
|
44 |
|
| (°C) |
|
|
|
|
|
|
Notes)
FAMAC-6: 2-(perfluorohexyl)ethyl methacrylate
FAAC-6: 2-(perfluorohexyl)ethyl acrylate
BzMA: benzyl methacrylate
PEGM: polyethylene glycol (n=4) monomethacrylate (PE-200)
VDC: vinylidene chloride
HEA: 2-hydroxyethyl acrylate
NMAM: N-methylol acrylamide
NMMA: N-methylol methacrylamide |
Example 1
[0045] To 2.0 parts by weight (corresponding to 0.5 parts by weight of the solid content)
of the aqueous dispersion A prepared in Reference Example 1, 0.375 parts by weight
(corresponding to 0.15 parts by weight of the solid content) of an aqueous emulsion
containing 2-butanone-o,o'[methylenebis(4,1-phenyleneaminocarboxy)]dioxime (abbreviation:
MDI-BTO) as the blocked isocyanate were added, followed by dilution with 97.625 parts
by weight of ion-exchanged water to give a water- and oil-repellent A.
Examples 2 to 4
[0046] In Example 1, a water- and oil-repellents B to D were prepared by using each of the
aqueous dispersions B to D, respectively prepared in Reference Examples 2 to 4, in
the same amount.
Example 5
[0047] In Example 1, a water- and oil-repellent E was prepared by changing the amount of
the aqueous emulsion of MDI-BTO as the blocked isocyanate to 1.25 parts by weight
and the amount of ion-exchanged water to 96.75 parts by weight.
Example 6
[0048] In Example 1, a water- and oil-repellent F was prepared by changing the amount of
the aqueous emulsion of MDI-BTO as the blocked isocyanate to 0.125 parts by weight
and the amount of ion-exchanged water to 97.875 parts by weight.
Comparative Example 1
[0049] A water- and oil-repellent G was prepared by diluting 2.0 parts by weight of the
aqueous dispersion A, prepared in Reference Example 1, with 98.0 parts by weight of
ion-exchanged water.
Comparative Examples 2 to 4
[0050] In Comparative Example 1, water- and oil-repellents H to J were prepared by using
each of the aqueous dispersions B to D, respectively prepared in Reference Examples
2 to 4, in the same amount.
[0051] To the thus obtained water- and oil-repellents A-J a cotton fabric, a cotton/polyester
blended fabric, a polyester fabric, or a nylon fabric was immersed therein for measuring
water-repellency (according to JIS L1092) and oil-repellency (according to AATCC-TM118-1992).
The wet pick-ups after squeezing were 80% for the cotton fabric and 100% for the cotton
blended fabric, 40% for the polyester fabric, and 60% for the nylon fabric. The drying
conditions were 80°C for 10 minutes, and the curing conditions were 150°C for 3 minutes,
for all the fabrics.
[0052] The evaluation criteria for water-repellency were defined in conformity with the
rules of the above-mentioned JIS.
| Degree of water-repellency |
Condition |
| 100 |
Showing no wet state and adhesion of water droplets on the surface |
| 90 |
Showing little adhesion of water droplets on the surface |
| 80 |
Partially showing separate wet state on the surface |
| 70 |
Showing wet state on a half area of the surface |
| 50 |
Showing wet state on the entire surface |
| 0 |
Showing complete wet state on both surfaces |
[0053] The evaluation criteria for oil-repellency were defined in conformity with the rules
of the above-mentioned AATCC. A drop of a test solution was dropped onto an oil-repellent
treated fabric, and conditions at 30 seconds after the dropping were investigated.
When the test solution dropped was held on the fabric, a test using a test solution
having a larger number was further conducted. The oil-repellency was evaluated with
the test solution that was the limit for being held on the fabric and on the basis
of the oil-repellency evaluation shown in the following table (when Nujol is not held
at all (100%), it is defined 0).
| Oil-repellency No. |
Test solution |
Surface tension (mN/m, 25°C) |
| 8 |
n-heptane |
20.0 |
| 7 |
n-octane |
21.8 |
| 6 |
n-decane |
23.5 |
| 5 |
n-dodecane |
25.0 |
| 4 |
n-tetradecane |
26.7 |
| 3 |
n-hexadecane |
27.3 |
| 2 |
Nujol/n-hexadecane (volume ratio: 65%:35%) |
29.6 |
| 1 |
Nujol |
31.2 |
[Washing resistance test]
[0054] A cotton fabric, a cotton/polyester blend fabric, a polyester fabric, or a nylon
fabric was each subjected to water- and oil-repellency treatment with each of the
water- and oil-repellents A to J, as described above, and then washed 5 times or 10
times according to the water washing method defined by JIS L0217, Appendix Table 103
and then air-dried, followed by evaluation for water-repellency and oil-repellency.
The evaluation results are shown in the form of water-repellency evaluation/oil-repellency
evaluation in the following Table 2.
Table 2
| |
|
Water-repellency evaluation/Oil-repellency evaluation |
| Example |
Water- and oil-repellent Fabric |
Cotton Fabric |
Blended Fabric |
Polyester Fabric |
Nylon Fabric |
| [Number of washing: 0 times] |
| Example 1 |
A |
100/1 |
100/4 |
100/4 |
100/5 |
| Example 2 |
B |
100/4 |
100/5 |
100/5 |
100/6 |
| Example 3 |
C |
100/5 |
100/5 |
100/6 |
100/6 |
| Example 4 |
D |
100/5 |
100/5 |
100/6 |
100/6 |
| Example 5 |
E |
100/4 |
100/5 |
100/5 |
100/6 |
| Example 6 |
F |
100/4 |
100/5 |
100/5 |
100/6 |
| Comp.Ex.1 |
G |
100/1 |
100/4 |
100/4 |
100/5 |
| Comp.Ex.2 |
H |
100/3 |
100/5 |
100/5 |
100/6 |
| Comp.Ex.3 |
I |
100/5 |
100/5 |
100/6 |
100/6 |
| Comp.Ex.4 |
J |
100/5 |
100/5 |
100/6 |
100/6 |
| [Number of washing: 5 times] |
| Example 1 |
A |
100/1 |
100/4 |
100/4 |
100/6 |
| Example 2 |
B |
100/4 |
100/5 |
100/5 |
100/6 |
| Example 3 |
C |
100/5 |
100/5 |
100/6 |
100/6 |
| Example 4 |
D |
100/4 |
100/5 |
100/6 |
100/6 |
| Example 5 |
E |
100/4 |
100/4 |
100/4 |
100/6 |
| Example 6 |
F |
100/3 |
100/5 |
100/5 |
100/6 |
| Comp.Ex.1 |
G |
70/0 |
80/1 |
100/4 |
100/5 |
| Comp.Ex.2 |
H |
70/2 |
100/4 |
100/5 |
100/6 |
| Comp.Ex.3 |
I |
70/3 |
100/4 |
100/6 |
100/6 |
| Comp.Ex.4 |
J |
70/3 |
100/4 |
100/6 |
100/6 |
| [Number of washing: 10 times] |
| Example 1 |
A |
70/1 |
100/3 |
100/4 |
100/5 |
| Example 2 |
B |
90/3 |
100/4 |
100/5 |
100/5 |
| Example 3 |
C |
90/3 |
100/4 |
100/6 |
100/6 |
| Example 4 |
D |
90/4 |
100/5 |
100/5 |
100/6 |
| Example 5 |
E |
90/3 |
100/4 |
100/5 |
100/5 |
| Example 6 |
F |
90/3 |
100/4 |
100/5 |
100/5 |
| Comp.Ex.1 |
G |
50/0 |
70/0 |
100/4 |
100/4 |
| Comp.Ex.2 |
H |
70/1 |
80/4 |
100/5 |
100/5 |
| Comp.Ex.3 |
I |
70/1 |
80/4 |
100/5 |
100/5 |
| Comp.Ex.4 |
J |
70/1 |
80/4 |
100/5 |
100/5 |