[0001] The present invention relates to a liquid detergent composition. In particular, the
present invention relates to a light-duty liquid detergent composition having an excellent
effect of preventing the shrinkage of clothes (effect of preventing felting shrinkage)
and also a good rinsability.
[Prior Art]
[0002] Delicate clothes made of wool or silk are usually washed by hands or a weak mechanical
power with a light-duty detergent so as to prevent the damage to them.
[0003] However, one often experiences that wool clothes particularly among these clothes
are apt to be shrunk (or cause felting shrinkage) even when they are mildly rubbed
or pressed in tepid water with meticulous care.
[0004] Conventional light-duty detergents of this type contain a polyoxyethylene alkyl ether,
polyoxyethylene alkyl ether sulfate, alkylbenzenesulfonate, etc., as the main detergent
base.
[0005] Recently, alkyl saccharide surfactants attract attention, since they little irritate
the skin and have lathering properties and, therefore, are usable as the light-duty
detergent base.
[0006] For example, Japanese Patent Laid-Open No. 501641/1988 discloses a detergent composition
for delicate cloths which contains an alkyl glycoside and an antistatic quaternary
ammonium surfactant, and Japanese Patent Laid-Open No. 501642/1988 describes that
a detergent composition for delicate cloths which contains an alkyl glycoside and
an antistatic amine oxide is capable of imparting antistatic properties superior to
those imparted when an ordinary polyoxyethylene alkyl ether is used. Japanese Patent
Laid-Open No. 69695/1989 discloses a detergent composition containing both of an alkyl
glycoside and an amphoteric surfactant and Japanese Patent Publication No. 168613/1989
discloses another detergent composition containing both of an alkyl glycoside and
a phosphoric ester surfactant, each composition having a good detergency, frothing
or lathering power and foam release property. JP-A No. 25896/1984 describes that a
detergent composition containing a nonionic surfactant having an HLB of 5 to 14, an
alkyl glycoside and a di-(long-chain alkyl) quaternary ammonium salt is quite effective
in removing stains in granular form and is capable of imparting softness and antistatic
properties to the clothes.
[0007] However, the shrinkage of wool products cannot be suppressed even by using these
detergents.
[0008] It is known that a light-duty detergent containing fine particles of a polymer latex
having a cationic or tertiary amino group and a particle diameter of 0.005 to 0.2
µm had a remarkable effect of inhibiting the felting shrinkage (see Japanese Patent
Laid-Open Nos. 8492/1988 and 89596/1988).
[0009] However, it is difficult to incorporate such a polymer latex into an alkyl glycoside
detergent composition stably.
( Summary of the invention )
[0010] After intensive investigations made for the purpose of solving the above-described
problems, the inventors have found that a detergent composition containing an alkyl
glycoside and a specified silicone compound has an excellent effect of inhibiting
the felting shrinkage, good frothing properties and improved rinsability. The present
invention has been completed on the basis of this finding.
[0011] Thus the present invention provides a liquid detergent composition for clothes comprising:
(a) 5 to 70% by weight of an alkyl glycoside and
(b) 0.05 to 5% by weight of an amino-modified silicone or a derivative thereof.
The alkyl glycosides used as the component (a) in the present invention are preferably
those represented by the following general formula (I):
R₁ (OR₂) xGy (I)
in which R₁ represents a straight-chain or branched alkyl, alkenyl or alkylphenyl
group having 8 to 18 carbon atoms, R₂ represents an alkylene group having 2 to 4 carbon
atoms, G represents a residue of a reducing sugar having 5 or 6 carbon atoms, and
x and y each represent an average number, x being 0 to 5 and y being 1 to 10.
[0012] From the viewpoints of the solubility, frothing properties and detergency, R₁ in
the general formula (I) preferably has 9 to 14 carbon atoms. From the viewpoint of
water solubility, R₂ has preferably 2 or 3 carbon atoms. The water solubility and
crystallizability vary depending on the value of
x. The higher the value of x, the higher the water solubility and the lower the crystallizability.
x is preferably in the range of 0 to 2, particularly 0.
y is preferably in the range of 1 to 4.
y is desirably selected in consideration of the properties ascribable to the hydrophobic
group R₁. For example, when R₁ is a hydrophobic group having 9 to 11 carbon atoms
on the average,
y is preferably 1 to 1.4, while when R₁ is a hydrophobic group having 12 to 14 carbon
atoms,
y is preferably 1.5 to 4.0. The average degree of polymerization,
y, of the reducing sugar can be determined by proton NMR.
[0013] The bonds in the sugar chain may be 1-2, 1-3, 1-4 or 1-6 bond, α- or β-pyranoside
bond or furanoside bond, or a combination of them.
[0014] The structure of G varies depending on the starting monosaccharide or polysaccharide.
The monosaccharides include glucose, fructose, galactose, xylose, mannose, lyxose
and arabinose. The polysaccharides include maltose, xylobiose, isomaltose, cellobiose,
gentiobiose, lactose, sucrose, nigerose, turanose, raffinose, gentianose and melezitose.
They can be used either alone or in combination of two or more of them. Glucose and
fructose are preferred among the monosaccharides and maltose and sucrose are preferred
among the polysaccharides, because they are easily available and inexpensive.
[0015] The amount of the component (a) is 5 to 70% by weight, preferably 10 to 40% by weight,
based on the composition.
[0016] Examples of the preferred amino-modified silicone or derivative thereof used as the
component (b) in the present invention are compounds of the following general formula
(II):

wherein:
R represents an alkyl group having 1 to 4 carbon atoms, a hydroxyl group or an alkoxy
group,
R₁ groups may be the same or different from one another and each represent an alkyl
group having 1 to 4 carbon atoms,
A represents R₁ or -(CH₂)
a-(OC₂H₄)
b-(OC₃H₆)
c-OR₂ in which:
a represents 2 or 3,
b and
c each represent 0 or 1 to 30 with the proviso that both of them do not represent 0
at the same time, and
R₂ represents an alkyl group having 1 to 24 carbon atoms;
B represents

in which:
d and
e each represent 2 to 6,
R₃ and R₄ each represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms,
X represents a hydrogen atom, an alkyl group having 1 to 24 carbon atoms or

R₅ being an alkyl group having 1 to 18 carbon atoms or -(CH₂)
f-(C₂H₄O)
g(C₃H₆O)
h-R₆,
f being 1 to 6,
g and
h each being 0 or 1 to 30 with the proviso that both of them do not represent 0 at
the same time, and R₆ being an alkyl group having 1 to 18 carbon atoms,
and
when X represents H or an alkyl group having 1 to 4 carbon atoms, one or two nitrogen
atoms may be quaternized.
[0017] Among the silicone compounds represented by the above general formula (II), those
wherein B represents

and X represents an alkyl group having 1 to 24 carbon atoms or

are preferred.
[0018] In the silicone compounds of the above general formula (II), those having a molecular
weight of 2,000 to 150,000 and amine equivalent in the range of 1,000 to 20,000 are
preferred and
m and
n are numbers variable depending on the molecular weight.
[0019] The amount of the component (b) is 0.05 to 5% by weight, preferably 0.1 to 3% by
weight, based on the composition.
[0020] It is well known that silicone compounds such as dimethylpolysiloxane can be incorporated
into detergents in a very small amount as a lathering regulator. Japanese Patent Laid-Open
No. 215099/1985 describes that when a small amount of an amino-modified silicone or
its derivative is incorporated into a detergent in a small amount, the clothes washed
therewith can be softened. However, these techniques neither teach nor suggest the
construction or effect of the present invention wherein an alkyl glycoside is used.
[0021] The balance of the composition of the present invention comprises water. When not
more than 50% by weight, preferably 10 to 50% by weight, based on the alkyl glycoside,
of another nonionic surfactant, particularly, a polyoxyethylene (having an average
molar number of addition of 5 to 20) alkyl (C₉ to C₁₄) ether is incorporated into
the composition, the deterging effect thereof is further improved without impairing
the effect of the present invention. Incorporation of a cationic surfactant is undesirable,
since its adsorbability on the clothes is higher than that of the modified silicone
and, therefore, the adsorption of the amino-modified silicone would be inhibited.
An anionic or amphoteric surfactant can be incorporated thereinto in only a small
amount (not more than 5% by weight, preferably not more than 1% by weight, based on
the composition).
[0022] The composition of the present invention may contain other components ordinarily
incorporated into such a light-duty detergent. They include antiredeposition agents
such as polyacrylic acid, polyvinylpyrrolidone, polyethylene glycol and carboxymethylcellulose;
enzymes such as protease, amylase, lipase and cellulase; enzyme stabilizers such as
calcium chloride; a solubilizing agent such as lower alcohols such as ethanol, benzenesulfonates
and lower alkylbenzenesulfonates such as p-toluenesulfonates, glycols such as propylene
glycol, benzoic acid salts and urea; antioxidants such as t-butylhydroxytoluene and
distyrenated cresol; as well as fluorescent dyes, bluing agents, perfumes and antibacterial
agents.
[0023] Up to 15 wt.%, preferably up to 10 wt.%, of the solubilizer may be used here to prevent
the phase separation. It is not needed when a small amount of a surfactant is only
used.
[0024] Although the composition of the present invention is desirably substantially free
from ordinary builders for detergents, not more than 2 or 3% by weight of a builder
component such as a diglycolic acid salt, phosphoric acid salt or carbonic acid salt
can be incorporated thereinto.
[Examples]
[0025] The following Examples will further illustrate the present invention, which by no
means limit the invention.
Example 1
[I] Determination of felting shrinkage rate and area shrinkage rate:
(1) Preparation of sample cloth:
[0026] A wool cloth, not yet treated for prevention of shrinking, having a size of 10 x
10 cm, three sides of which had been hemstitched with a lockstitch machine was immersed
in city water at ambient temperature for 30 min, then dewatered in a dewatering tank
of a washing machine for 30 sec, dried on a net and kept at 20°C and 65% RH for at
least 4 h. The cloth was marked at four points with an oil-base felt pen and numbers
were given to the marks. The distances between the marks (a

and a

in the direction of the length and b

and b

in the direction of the width) were measured. The distances will be called the "original
length".
(2) Washing method:
[0027] Three sample cloths prepared in the above step (1) were placed in a pot and washed
with a Terg-O-Tometer (mfd. by Ueshima Seisakusho Co., Ltd.) at a rate of 120 r.p.m.
for 10 min. The detergent concentration was 0.25% by weight and the water temperature
was 20°C. They were then rinsed with running water in a pot and then with running
water in a washbasin. Thereafter, the cloths were pressed on the walls of the dewatering
tank of the washing machine and dewatered for 30 sec, dried on the net, and kept at
20°C and 65% RH for at least 4 h.
[0028] Then the distances between the marks marked in the above-described step (1) (a

and a

in the direction of the length and b

and b

in the direction of the width) were measured. The felting shrinkage rate and area
shrinkage rate were calculated according to the following equations, respectively.
The results are given in Table 1.
<Calculation of felting shrinkage rate (according to IWS TM 9)>
[0029] 
wherein R.M. represents the distances measured before washing (original length) and
W.M. represents the distance measured after washing.
<Calculation of area shrinkage rate>
[0030] 
wherein W.S. represents the felting shrinkage in the direction of the width and L.S.
represents the felt shrinkage in the direction of the length.
[II] Evaluation of latheriness and rinsability:
[0031] 5 ℓ of city water at 30°C was placed in a 10-ℓ basin. 100 g of a piece of the untreated
wool cloth and 100 g of an acrylic jersey cloth (200 g in total) and 12.5 mℓ of a
detergent were placed therein. After washing for 5 min, the cloths were dewatered
with a dewatering machine for 30 sec. 5 ℓ of city water at 30°C was added thereto
and the cloths were rinsed by repeatedly pressing them in water for 1 min.
[0032] The height (cm) of the lather 5 min after the washing and that 1 min after the press
rinsing were macroscopically observed and evaluated according to the following criteria:
rinse index:
- 5:
- lather remained on the whole water surface,
- 4:
- lather remained on 1/2 of the water surface,
- 3:
- lather remained on 1/4 of the water surface,
- 2:
- fine lather remained on the water surface,
and
- 1:
- no lather remained on the water surface.
Alkyl glycoside (1):
general formula (I) wherein:
R₁ = C₉ to C₁₁, x = 0, y = 1.35,
G: glucose residue,
Alkyl glycoside (2):
general formula (I) wherein:
R₁ = C₁₂, x = 0, y = 1.7,
G: glucose residue,
Silicone (1):
general formula (II) wherein:
R, R₁ and A: CH₃,

having a molecular weight of 14,000 and an amine equivalent of 4,500,
Silicone (2):
general formula (II) wherein:
A, R₁ and A: CH₃,

having a molecular weight of 20,000 and an amine equivalent of 1,000,
Silicone (3):
general formula (II) wherein:
R, R₁ and A: CH₃,
B: -(CH₂)₃-NH-(CH₂)-NH-C₁₂H₂₅
having a molecular weight of 7,000 and an amine equivalent of 2,300,
Silicone (4):
dimethylpolysiloxane having a molecular weight of 10,000 and an amine equivalent of
0.
Example 2
[0033] Detergent compositions listed in Table 2 were prepared to evaluate the detergency
by the following method wherein the alkyl glycoside (1) and silicone (1) were the
same as those used in Example 1:

[0034] 1 kg of the above-described composition was dissolved or dispersed in 80 ℓ of Perclene
and a shirting 2023 cloth was immersed therein to adhere the stain to the cloth. Then
Perclene was dried and removed. Perclene is the tradename of perchloroethylene.
Washing conditions and evaluation method:
[0035] Five cotton cloths (artificially stained cloth) having a size of 10 cm x 10 cm which
had been stained with sebum/carbon were placed in 1 ℓ of an aqueous detergent solution
prepared for the evaluation and washed with a Terg-O-Tometer at 100 r.p.m. under the
following washing conditions:
<washing conditions>

[0036] The detergency was determined by measuring the reflectivity of the original cloth
before staining and those of the stained cloth before and after washing with an autographic
colorimeter (mfd. by Shimadzu Corp. to calculate the deterging rate (%) according
to the following equation (the average of the five samples is given in the Table):

[0037] The results are given in Table 2.
