Compositions for activating an inorganic peroxide bleaching agent

Nakagawa , et al. August 26, 1

Patent Grant 3901819

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] 47-92265
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
3163606 December 1964 Vireen et al.
3211658 October 1965 Hirtz et al.
3338839 August 1967 MacKellar et al.
3650962 March 1972 Werdehausen et al.
3661789 May 1972 Corey et al.
3840466 August 1974 Gray
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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