U.S. patent number 3,901,819 [Application Number 05/395,264] was granted by the patent office on 1975-08-26 for compositions for activating an inorganic peroxide bleaching agent.
This patent grant is currently assigned to Kao Soap Co., Ltd.. Invention is credited to Shori Hakozaki, Yunosuke Nakagawa, Koitsu Sato.
United States Patent |
3,901,819 |
Nakagawa , et al. |
August 26, 1975 |
Compositions for activating an inorganic peroxide bleaching
agent
Abstract
A composition for activating an inorganic peroxide bleaching
agent comprising (A) an acetic acid ester of a monosaccharide, a
disaccharide, a sugar alcohol, an internal anhydride of a sugar
alcohol, or erythritol, said ester having at least 2 ester groups
on the adjacent carbon atoms, and (B) an acetic acid ester of a
polyhydric alcohol having a melting point not higher than about
30.degree.C., the weight ratio of the components being within the
range of from 1/9 to 9/1.
Inventors: |
Nakagawa; Yunosuke (Koshigaya,
JA), Sato; Koitsu (Funabashi, JA),
Hakozaki; Shori (Funabashi, JA) |
Assignee: |
Kao Soap Co., Ltd. (Tokyo,
JA)
|
Family
ID: |
14049556 |
Appl.
No.: |
05/395,264 |
Filed: |
September 7, 1973 |
Foreign Application Priority Data
|
|
|
|
|
Sep 14, 1972 [JA] |
|
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47-92265 |
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Current U.S.
Class: |
252/186.4; 8/111;
252/186.41; 510/312; 510/376; 510/378; 510/470; 510/505; 510/506;
510/441; 252/186.38 |
Current CPC
Class: |
D06L
4/12 (20170101); C11D 3/3912 (20130101); C11D
3/391 (20130101) |
Current International
Class: |
C11D
3/39 (20060101); D06L 3/02 (20060101); D06L
3/00 (20060101); C11D 007/54 (); C11D 007/18 () |
Field of
Search: |
;252/186,99 ;8/111
;260/61A,61R |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Padgett; Benjamin R.
Assistant Examiner: Gluck; Irwin
Attorney, Agent or Firm: Woodhams, Blanchard and Flynn
Claims
The embodiments of the invention in which an exclusive property or
privilege is claimed are defined as follows:
1. An activating agent composition for activating an inorganic
peroxide bleaching agent, consisting essentially of
A. acetic acid ester of a substance selected from the group
consisting of a monosaccharide, a disaccharide, a sugar alcohol, an
internal anhydride of a sugar alcohol, erythritol and mixtures
thereof, said ester having at least two ester groups on adjacent
carbon atoms of said substance, and
B. acetic acid ester of polyhydric alcohol having a melting point
not higher than about 30.degree.C, the weight ratio of A:B being
from 1:9 to 9:1.
2. A composition according to claim 1, in which ingredient A is an
acetic acid ester of substance selected from the group consisting
of glucose, mannose, galactose, fructose, arabinose, xylose,
sucrose, lactose, maltose, sorbitol, mannitol, sorbitan, mannitan,
xylitol, arabitol, and xylitan and mixtures thereof.
3. A composition according to claim 1, in which ingredient A is
selected from the group consisting of glucose pentacetate, glucose
tetracetate, fructose pentacetate, sucrose octacetate, sorbitol
hexacetate, sorbitan tetracetate, mannitol hexacetate, mannitan
tetracetate, xylitol pentacetate, xylitan triacetate and erythritol
tetracetate.
4. A composition according to claim 1, in which ingredient B is an
acetic acid ester of polyhydric alcohol selected from the group
consisting of ethylene glycol, propylene glycol, butylene glycol,
glycerin and diglycerin.
5. A composition according to claim 1, in which ingredient B is
selected from the group consisting of triacetin and ethylene glycol
diacetate.
6. A bleaching composition comprising (1) an inorganic peroxide
bleaching agent capable of releasing hydrogen peroxide in an
aqueous solution, and (2) an activating agent composition as
defined in claim 1, in which the weight ratio of (1):(2) is from
1:9 to 9:1.
7. A bleaching composition according to claim 6, in which
ingredient (1) is selected from the group consisting of hydrogen
peroxide, sodium perborate, sodium percarbonate, sodium
peroxypyrophosphate and sodium peroxysilicate.
Description
BACKGROUND OF THE INVENTION
1. FIELD OF THE INVENTION
This invention relates to an activating composition for
intensifying the bleaching activity of an inorganic peroxide
bleaching agent at low temperatures.
2. DESCRIPTION OF THE PRIOR ART
When an inorganic peroxide bleaching agent such as sodium perborate
is used by itself at a high temperature, such as 80.degree.C. or
above, it exhibits a very high bleaching activity. But at a low
temperature, such as 40.degree.C. or below, its bleaching effect is
extremely low. Accordingly, various studies have heretofore been
made on so-called activating agents for intensifying the bleaching
effect of such inorganic peroxide bleaching agents at low
temperatures.
Because the waste liquors from the bleaching treatment steps are
discarded without further treatment, it is desired that such
activating agents be readily biologically decomposable. It is also
desired that they be non-poisonous.
As conventional activating agents meeting these requirements, there
can be mentioned acetic acid esters of sugars and sugar alcohols.
In these acetic acid esters, a sufficient effect cannot be obtained
by partially esterified compounds, and hence, all of the hydroxyl
groups should be esterified with acetic acid.
However, since such completely esterified compounds have a very low
water solubility, when the washing is conducted at a low
temperature (for instance, 20.degree.C.) for a short time (for
instance, 10 minutes), a sufficient bleaching effect cannot be
obtained.
SUMMARY OF THE INVENTION
We have found, unexpectedly in view of the prior art, that when an
acetic acid ester of a polyhydric alcohol having a melting point
not higher than about 30.degree.C. is added to an acetic acid ester
of a sugar or sugar alcohol, not only is the water solubility
increased but also the activating effect is greatly enhanced.
This invention provides a composition for activating an inorganic
peroxide bleaching agent which consists essentially of (A) an
acetic acid ester of a monosaccharide, a disaccharide, a sugar
alcohol, an internal anhydride of a sugar alcohol, or erythritol,
and mixtures thereof, said ester having at least 2 ester groups on
the adjacent carbon atoms, and (B) an acetic acid ester of a
polyhydric alcohol having a melting point not higher than
30.degree.C., the weight ratio of A:B being within the range of
from 1:9 to 9:1, preferably 1:3 to 3:1, especially about 1:1.
Acetic acid esters of monosaccharides, disaccharides, sugar
alcohols, internal anhydrides of sugar alcohols and erythritol
employed in this invention include acetic acid esters of hexoses
such as glucose, mannose, galactose and fructose; pentoses such as
arabinose and xylose; disaccharides such as sucrose, lactose and
maltose; hexitols such as sorbitol and mannitol; internal
anhydrides of hexitols, i.e., hexitan, such as sorbitan and
mannitan; pentitols such as xylitol and arabitol; internal
anhydrides of pentitols, i.e., pentitans, such as xylitan; and the
like. These acetic acid esters should have at least 2 ester groups
on adjacent carbon atoms and they can be up to 100% esterified.
Specific examples of such acetic acid esters are glucose
pentacetate, glucose tetracetate, fructose pentacetate, sucrose
octacetate, sorbitol hexacetate, sorbitan tetracetate, mannitol
hexacetate, mannitan tetracetate, xylitol pentacetate, xylitan
triacetate and erythritol tetracetate.
Acetic acid esters of polyhydric alcohols having a melting point
not higher than 30.degree.C., which are used in the composition of
this invention, include acetic acid esters of ethylene glycol,
propylene glycol, butylene glycol, glycerin and diglycerin.
It is preferred that these esters have a degree of esterification
of 100%. Glycerine triacetate, i.e., triacetin, and ethylene glycol
diacetate are especially preferred, because they have an activity
of activating an inorganic peroxide bleaching agent.
Tetracetyl ethylenediamine is an activating agent of low water
solubility, like the acetic acid esters of sugars and sugar
alcohols employed in this invention. But in this case of tetracetyl
ethylenediamine, an improved effect cannot be obtained by mixing it
with, for example, triacetin. The specific synergistic effects of
(1) improving the water solubility and (2) enhancing the activating
property, that characterize the composition of this invention, can
be attained only by employing a combination of an acetic acid ester
of a sugar or sugar alcohol etc. as set forth above and an acetic
acid ester of a polyhydric alcohol having a melting point not
higher than 30.degree.C.
The activating composition of this invention can be directly added
to a bleaching liquor containing an inorganic peroxide, or it can
be incorporated in advance into an inorganic peroxide bleaching
agent. In the latter case, the composition can be kneaded with a
granulating agent such as polyethylene glycol 6000 and formed into
granules having flowability. The composition may further comprise
surfactants such as anionic surfactants, non-ionic surfactants and
amphoteric surfactants, neutral inorganic salts such as sodium
sulfate, alkaline inorganic salts such as sodium tripolyphosphate,
heavy metal chelating agents such as sodium nitrilotriacetate,
redeposition-preventive agents such as carboxymethyl cellulose,
perfumes, fluorescent dyes, and the like.
Inorganic peroxide bleaching agents to which the composition of
this invention can be applied are substances capable of releasing
hydrogen peroxide in an aqueous solution. Examples of such
bleaching agents are hydrogen peroxide, sodium perborate, sodium
percarbonate, sodium peroxypyrophosphate and sodium
peroxysilicate.
The mixing ratio of the activating composition of this invention to
the inorganic peroxide is within the range of from 1/9 to 9/1 on
the weight basis. When the bleaching agent is used at a low
temperature for a short time, it is preferred that the proportion
of the activating composition is increased. It is also preferred
that when the bleaching agent is used at a relatively high
temperature for a long time, the proportion of the activating
composition is reduced.
This invention will now be further described by reference to the
following illustrative examples, in which all references to "parts"
and percent % are on a weight basis.
EXAMPLE 1
The activating agents listed in the following Table 1 were
respectively added in an amount of 0.5 part to 100 parts of a 0.5%
aqueous solution of sodium perborate. The state of dissolution of
the activating agent was examined after the mixture had been
allowed to stand still at 20.degree.C. for 1 minute. Then a
bleaching test was conducted at 20.degree.C. for 10 minutes. The
results obtained are shown in the following Table 1.
The bleaching test was carried out as follows: Three soiled cloths
for the bleaching test (cloth of 10 cm .times. 7 cm soiled with
tea) were put into a Terg-O-Tometer and subjected to rotating
agitation at 100 rpm, at 20.degree.C for 10 minutes. The cloths
were then rinsed with city water, air-dried and ironed.
The effectiveness of compositions was determined by measuring the
reflectivities of the cloths before and after the treatment.
Bleaching Force: The bleaching force is expressed in terms of the
value of ((reflectivity of bleached cloth) - (reflectivity of
untreated cloth)).
Table 1
__________________________________________________________________________
Run No. Activating Agent (weight ratio) Form of Activating
Dissolving State Bleaching Force Agent After 1 Minute
__________________________________________________________________________
(control) glucose pentacetate/triacetin powder suspended 12.8
(100/0) (powder not dis- solved) 2 glucose pentacetate/triacetin
powder slightly suspended 15.0 (75/25) (powder mostly dissolved) 3
glucose pentacetate/triacetin powder substantially dis- 18.6
(50/50) solved (powder al- most entirely dis- solved) 4 glucose
pentacetate/triacetin paste completely dis- 13.2 (25/75) solved 5
glucose pentacetate/triacetin liquid completely dis- 10.6 (control)
(0/100) solved 6 not added -- -- 2.1 (control)
__________________________________________________________________________
EXAMPLE 2
In each test, 0.5 part of an activating agent listed in the
following Table 2 was added to 100 parts of a bleaching agent
aqueous solution containing 1.0% of sodium percarbonate, 0.05% of
sodium dodecylbenzenesulfonate and 1.0% of sodium tripolyphosphate.
The bleaching test was conducted in the same manner as in Example 1
and the results shown in the following Table 2 were obtained.
Table 2
__________________________________________________________________________
Run No. Activating agent (Weight ratio) Bleaching Force
__________________________________________________________________________
7 (control) sorbitol hexacetate/ethylene 13.6 glycol diacetate
(100/0) 8 sorbitol hexacetate/ethylene 17.5 glycol diacetate
(50/50) 9 sorbitol hexacetate/ethylene 8.5 (control) glycol
diacetate (0/100) 10 tetracetylethylene diamine/ 14.2 (control)
ethylene glycol diacetate (100/0) 11 tetracetylethylene diamine/
(control) ethylene glycol diacetate (50/50) 11.5 12
tetracetylethylene diamine/ 8.5 (control) ethylene glycol diacetate
(0/100) 13 not added 5.6 (control)
__________________________________________________________________________
From the above results, it is seen that a mixture of sorbitol
hexacetate and ethylene glycol diacetate exhibits a synergistic
effect, whereas ethylene glycol diacetate is ineffective when
combined with tetracetylethylene diamine.
EXAMPLE 3
50 Parts of sucrose octacetate was mixed with 50 parts of
diglycerin tetracetate. Then 100 parts of corn starch and 100 parts
of polyethylene glycol were added to the mixture. The resulting
composition was granulated by means of a pelletizer having an
orifice diameter of 0.7 mm to obtain a granular activating
composition. Using the thus-formed activating composition, a
powdery bleaching agent was prepared according to the following
recipe:
sodium perborate 30 parts sodium tripolyphosphate 15 parts sodium
carbonate 10 parts sodium metasilicate 2 parts sodium laurylsulfate
5 parts sodium sulfate 3 parts above activating composition 35
parts
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