BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to an economical water- and oil-repellent composition
having good water- and oil-repellency.
Description of the Related Arts
[0002] A water- and oil- repellent having a fluoroalkyl group has better properties than
other conventional water- and oil-repellent, and is widely used. However, it is relatively
expensive. In order to decrease the cost, it is proposed to replace a part of the
water- and oil repellent having the fluoroalkyl group with a cheap acrylic acid base
polymer or polyhydric alcohol such as sorbitol and lactose while keeping the water-
and oil-repellency (cf. Japanese Patent Publication Nos. 22487/1963, 8579/1966 and
4160/1978). Although reduction of the cost is achieved to some extent while keeping
the water- and oil- repellency, the above proposal is not satisfactory.
SUMMARY OF THE INVENTION
[0003] An object of the present invention is to provide an economical water- and oil-repellent
composition having sufficient water- and oil-repellency.
[0004] This and other objects of the present invention are achieved by a water- and oil-repellent
composition which comprises a water- and oil-repellent having a fluoroalkyl group,
and a glycerol compound selected from the group consisting of glycerol, an ester
derivative of glycerol, an ether derivative of glycerol and polyglycerol having a
melting point of lower than 70°C.
DETAILED DESCRIPTION OF THE INVENTION
[0005] The ester derivative of glycerol is preferably an ester prepared by esterifying a
hydroxyl group at the α-position with a monoalkane acid having 1 to 6 carbon atoms,
for example, glycerol α-monoacetate, glycerol α-monoformate and glycerol α-mono-n-hexanoate.
The ether derivative of glycerol is preferably an ether prepared by substituting a
hydrogen of a hydroxyl group at the α-position with an alkyl group having 1 to 6 carbon
atoms, for example, glycerol α-monomethyl ether, glycerol α-monoethyl ether and glycerol
α-monoisopropyl ether.
[0006] In the composition of the present invention, a ratio of the glycerol compound to
the water- and oil-repellent is not critical and varies in a wide range dependent
on other conditions such as the kinds of the water- and oil-repellent and the glycerol
compound. When rhe amount of the glycerol compound is too large, the water- and oil-repellent
composition has deteriorated properties. When the amount of the glycerol compound
is too small, the cost is not reduced and the water- and oil-repellency is not improved.
Accordingly, the glycerol compound is usually used in an amount of 0.05 to 7 parts
by weight, preferably 0.1 to 4 parts by weight per one part by weight of the water-
and oil-repellent.
[0007] The amount of the water- and oil-repellent having the fluoroalkyl group is not limited.
The water- and oil-repellent having the fluoroalkyl group is usually used in an amount
of 0.1 to 1.0 per 100 parts by weight of a medium.
[0008] The water- and oil-repellents include a homopolymer of an acrylate or methacrylate
having a fluoroalkyl group having 4 to 21 carbon atoms and a copolymer thereof with
a monomer having no fluoroalkyl group (cf. for example, Japanese Patent Publication
8068/1985).
[0009] Preferable acrylate and methacrylate having the fluoroalkyl group are as follows:
R
f(CH₂)
mOCOCR¹=CH₂ and
R
fSO₂NR²(CH₂)
mOCOR¹=CH₂
wherein R
f is a perfluoroalkyl group having 4 to 21 carbon atoms, R¹ is hydrogen or a methyl
group, R² is an alkyl group having 1 to 10 carbon atoms, and m is an integer of 1
to 10.
[0010] Specific examples of the acrylate and methacrylate having the fluoroalkyl group are
as follows:
CF₃(CF₂)₇(CH₂)₁₁OCOCH=CH₂
CF₃(CF₂)₄CH₂OCOC(CH₃)=CH₂
CF₃(CF₂)₆(CH₂)₂OCOC(CH₃)=CH₂
CF(CF₃)₂(CF₂)₆(CH₂)₃OCOCH=CH₂
CF(CF₃)₂(CF₂)₁₀(CH₂)₃OCOCH=CH₂
CF₃(CF₂)₇SO₂N(C₃H₇)(CH₂)₂OCOCH=CH₂
CF₃(CF₂)₇SO₂N(CH₃)(CH₂)₂OCOC(CH₃)=CH₂
CF(CF₃)₂(CF₂)₆CH₂CH(OH)CH₂OCOCH=CH₂
CF(CF₃)₂(CF₂)₆CH₂CH(OCOCH₃)OCOC(CH₃)=CH₂
CClF₂(CF₂)₁₀CH₂OCOC(CH₃)=CH₂
H(CF₂)₁₀CH₂OCOCH=CH₂
In addition to the above, the monomer having the fluoroalkyl group of the formula:
CF(CF₃)(CClF₂)(CF₂)₇CONHCOOCH=CH₂
can be used alone or in addition to the above methacrylate or acrylate.
[0011] Specific examples of the monomer having no fluoroalkyl group are ethylene, vinyl
acetate, vinyl fluoride, vinyl chloride, vinylidene fluoride, vinylidene chloride,
acrylonitrile, styrene, α-methylstyrene, p-methylstyrene, acrylic acid and alkyl esters
thereof, methacrylic acid and alkyl esters thereof, acrylamide, diacetone acrylamide,
methylol diacetone acrylamide, methylol diacetone methacrylamide, vinyl alkyl ether,
vinyl alkyl ketone, butadiene, isoprene, chloroprene, glycidyl acrylate, maleic anhydride
and the like. The monomer having no fluoroalkyl group is usually used in an amount
of 0 to 75, preferably 20 to 65 parts by weight per 100 parts by weight of the polymer.
[0012] The homopolymer and copolymer of the above acrylate and methacrylate may be prepared
by bulk polymeri zation, solution polymerization, emulsion polymerization and the
like. The emulsion polymerization is usually preferable. Accordingly, a medium is
usually water. The emulsion polymerization uses no specific procedure. For example,
as described in Japanese Patent Publication No. 8068/1985, a mixture of monomers is
emulsified in the presence of a surfactant and a polymerization initiator, and then
polymerized at 50 to 100°C with stirring. The initiator includes a peroxide, an azo
compound and a persulfate. As the surfactant, any of anionic, cationic and nonionic
surfactants can be used. A mixture of at least one cationic surfactant and at least
one nonionic surfactant is preferable.
[0013] The composition of the present invention may include conventionally used additives,
for example, a crosslinking agent, an antistatic agent, a dye fixing agent, an anticrease
agent, a flame retardant, a mothproofing agent and the like, and it may include general-purpose
organic solvents, for example, isopropanol and the like.
[0014] The water- and oil-repellent composition of the present invention may be applied
on a material to be treated by conventionally known methods such as spraying, dipping
and the like.
[0015] The materials to be treated include natural and synthetic fibers and textiles. An
adsorption amount of the water- and oil-repellent to the material to be treated is
preferably 0.01 to 2% by weight based on the material to be treated.
[0016] When a polyhydric alcohol, an ester or ether derivative of the polyhydric alcohol,
or polyglycerol having the melting point of not lower than 70°C which is not included
in the glycerol compound of the present invention is used in the water- and oil-repellent
composition, an effect is observed to some extent but various defects arise. For example,
the ester or ether derivative of a polyhydric alcohol having more carbon atoms or
hydroxyl groups than glycerol remains in a cloth in a large amount after the water-
and oil-repellency treatment, and the water- and oil-repellency property decreases
due to hydrophilic hydroxyl groups and lipophilic alkyl groups. In addition, the treated
cloth has deteriorated feeling. An ester or ether derivative of a polyhydric alcohol
or alcohol having fewer carbon atoms or hydroxyl groups than glycerol cannot increase
the water- and oil-repellency. The polyglycerol having the melting point of not lower
than 70°C has the same defects as above.
[0017] The water- and oil-repellent composition according to the present invention is economical
since the glycerol compound used as the blending component is more easily available
than the conventional blending component which comprises the acrylic resin.
[0018] In addition, when the conventional water- and oil- repellent is added in a small
amount, the water- and oil-repellency is usually insufficient. But, according to
the present invention, the water- and oil-repellency is sufficient because of the
use of the glycerol compound even if the water- and oil-repellent adheres to a cloth
in a small amount.
[0019] The present invention will be illustrated by following Examples. The Examples, of
course, do not restrict the present invention.
[0020] The water- and oil-repellent composition was evaluated as follows:
[0021] The warer repellency is expressed by the water repellency No. of Table 1 determined
by the spray method according to JIS (Japanese Industrial Standard) L-1092. Oil repellency
is expressed by the oil repellency No. of Table 2 determined by dropping several drops
(diameter: about 4 mm) of a test solvent on two positions of a surface of a test cloth
and observing whether the drops are held on the surface for 30 seconds or not. The
superscript "+" to the water repellency No. represents that the result is slightly
better than said water repellency No.
[0022] Feeling is evaluated by measuring the rigidity and softness of the cloth by the Handle-O-meter
method according to JIS L-1096.
[0023] Resistance to washing is expressed by the water- and oil-repellency Nos. which are
determined after carrying out five cycles each consisting of washing a cloth treated
with the water- and oil-repellent composition at 40°C in water containing 0.3 % by
weight of detergent (Zabu-koso XK, manufactured by Kao) with a bath ratio of 1:40
(cloth:washing liquid (g:g)) for 5 minutes by using a domestic washing machine followed
by rinsing the cloth for 15 minutes, dehydrating it and drying it at room temperature.
[0024] Resistance to dry cleaning is expressed by the water- and oil-repellency Nos. which
are determined by washing a cloth treated with the water- and oil-repellent composition
at 30°C in tetrachloroethylene by using a Launder-O-meter followed by drying at room
temperature and then measuring the water- and oil-repellency.
Table 1
Water repellency No. |
State |
100 |
No wet on the surface |
90 |
Slight wet on the surface |
80 |
Drop like wet on the surface |
70 |
Considerable wet on the surface |
50 |
Wet over the whole surface |
0 |
Complete wet of the surface and backface |
Table 2
Oil repellency No. |
Test solvent |
Surface tension |
|
|
(dyne/cm, 25°C) |
8 |
n-Heptane |
20.0 |
7 |
n-Octane |
21.3 |
6 |
n-Decane |
23.5 |
5 |
n-Dodecane |
25.0 |
4 |
n-Tetradecane |
26.7 |
3 |
n-Hexadecane |
27.3 |
2 |
n-Hexadecane/Nujol (35/65 by weight) |
29.6 |
1 |
Nujol |
31.2 |
0 |
Nujol penetrated |
|
Examples 1 to 4 and Comparative Examples 1 to 3
[0025] A water- and oil-repellent used in the water- and oil-repellent composition of the
present invention was prepared as follows:
[0026] The compound (60 g) of the formula:
(CF₃)₂CF(CF₂CF₂)
nCH₂CH₂OOCCH=CH₂
(mixture of n = 3, 4 and 5 in a weight ratio of 5:3:1),
C₁₈H₃₇OOCCH=CH₂ (38 g), CH₂=CHCOOCH₂CH(OH)CH₂Cl (2 g), pure water (250 g), acetone
(50 g), n-dodecyl mercaptan (0.2 g) dimethylalkylamine acetate salt (3 g) and polyoxyethylenealkylphenol
(3 g) were charged in a flask, and stirred at 60°C for one hour under a nitrogen stream.
A solution of azobisisobutylamidine hydrochloride (1 g) in water (10 g) was added
and the copolymerization was carried out while stirring at 60°C for 5 hours under
the nitrogen stream. According to a gas chromatography, a conversion of copolymerization
was not lower than 99%. From this conversion, a ratio of the repeating units of the
resultant copolymer was found to be substantially almost the same as a ratio of the
charged monomers. The resultant emulsion contained the copolymer in the solid content
of 25 %.
[0027] The emulsion was mixed with the blending components as shown in Table 3 to prepare
water- and oil-repellent compositions.
[0028] Test cloths were a polyester finished yarn woven fabric (hereinafter referred to
as PE) and a nylon taffeta fabric (hereinafter referred to as N), and were dipped
in the above composition for one minute and squeezed between two rolls so as to adjust
the water content at 90 % and 50 %, respectively. Then, they were dried at 110°C for
three minutes, PE was thermally treated at 180°C for 40 seconds and N was thermally
treated at 170°C for one minute to impart the water- and oil-repellency. The water-
and oil-repellency of the treated cloths were measured. The results are shown in
Table 4.
[0029] As is clear from Table 4, when the glycerol compound of the present invention is
added to the water- and oil-repellent composition, good water- and oil-repellency
is achieved.
Table 3
Example No. |
Test cloth |
Adhesion of repellent to fabric (wt%) |
Blending component |
Adhesion of blending component to fabric (wt%) |
1 |
PE |
0.03 |
Glycerol |
0.015 |
|
N |
0.10 |
0.05 |
2 |
PE |
0.03 |
Glycerol α-monomethyl ether |
0.015 |
|
N |
0.10 |
0.05 |
3 |
PE |
0.03 |
Glycerol α-monoacetate |
0.015 |
|
N |
0.10 |
0.05 |
4 |
PE |
0.03 |
Polyglycerol (melting point: 30°C) (molecular weight: 170) |
0.015 |
|
N |
0.10 |
0.05 |
Comp.1 |
PE |
0.03 |
- |
- |
|
N |
0.10 |
- |
Comp.2 |
PE |
0.03 |
Sorbitol |
0.015 |
|
N |
0.10 |
0.05 |
Comp.3 |
PE |
0.03 |
Polyglycerol (melting point: >70°C) (molecular weight: 1000) |
0.015 |
|
N |
0.10 |
0.05 |
Table 4
Example No. |
Test cloth |
Initial |
After washing |
After dry cleaning |
Feeling |
|
|
Water repellency/Oil repellency |
Water-repellency/Oil-repellency |
Water-repellency/Oil-repellency |
(blank: 10 g) |
1 |
PE |
100⁺/7 |
50/0 |
80/3 |
8 |
|
N |
100⁺/2 |
50/0 |
70/0 |
|
2 |
PE |
100⁺/7 |
50/0 |
80/3 |
8 |
|
N |
100⁺/1 |
50/0 |
70/0 |
|
3 |
PE |
100⁺/6 |
50/0 |
80/2 |
8 |
|
N |
100⁺/1 |
50/0 |
70/0 |
|
4 |
PE |
100⁺/5 |
50/0 |
80/20 |
8 |
|
N |
100/0 |
0/0 |
70/0 |
|
Comp.1 |
PE |
80⁺/5 |
0/0 |
70/2 |
9 |
|
N |
80/0 |
0/0 |
50/0 |
|
Comp.2 |
PE |
90/5 |
50/0 |
70⁺/2 |
12 |
|
N |
90/0 |
50/0 |
70/0 |
|
Comp.3 |
PE |
80⁺/5 |
0/0 |
70⁺/2 |
10 |
|
N |
80⁺/0 |
0/0 |
50⁺/0 |
|
1. A water- and oil-repellent composition which comprises a water- and oil-repellent
having a fluoroalkyl group, and a glycerol compound selected from the group consisting
of glycerol, an ester derivative of glycerol, an ether derivative of glycerol and
polyglycerol having a melting point of lower than 70°C.
2. The water- and oil-repellent composition according to claim 1, wherein the ester
derivative of glycerol is an ester prepared by esterifying a hydroxyl group at the
α-position with a monoalkane acid having 1 to 6 carbon atoms.
3. The water- and oil-repellent composition according to claim 1, wherein the ether
derivative of glycerol is an ether prepared by substituting a hydrogen of a hydroxyl
group at the α-position with an alkyl group having 1 to 6 carbon atoms.
4. The water- and oil-repellent composition according to claim 1, wherein the water-
and oil-repellent is a homopolymer of an acrylate or methacrylate having a fluoroalkyl
group having 4 to 21 carbon atoms or a copolymer thereof with a monomer having no
fluoroalkyl group.
5. The water- and oil-repellent composition according to claim 1, wherein the composition
contains the glycerol compound in an amount of 0.05 to 7 parts by weight per one part
by weight of the water- and oil-repellent.