CA1284447C - Chlorine stable detergent compositions containing non-ionic surfactants - Google Patents
Chlorine stable detergent compositions containing non-ionic surfactantsInfo
- Publication number
- CA1284447C CA1284447C CA000522094A CA522094A CA1284447C CA 1284447 C CA1284447 C CA 1284447C CA 000522094 A CA000522094 A CA 000522094A CA 522094 A CA522094 A CA 522094A CA 1284447 C CA1284447 C CA 1284447C
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- groups
- bisphenol
- composition
- percent
- oxyalkylene
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3707—Polyethers, e.g. polyalkyleneoxides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
Abstract
DETERGENT COMPOSITION
Abstract of the Disclosure The instant invention relates to a composition comprising a Bisphenol initiated polyoxyalkylene compound, a chlorine releasing compound and water. This composition has varied uses as a fabric cleaner with bleaching properties, a warewashing composition having a minimum of odor problems.
Accordingly, in addition to the above components the invention relates to compositions which may also contain conventional ingredients for such compositions.
Abstract of the Disclosure The instant invention relates to a composition comprising a Bisphenol initiated polyoxyalkylene compound, a chlorine releasing compound and water. This composition has varied uses as a fabric cleaner with bleaching properties, a warewashing composition having a minimum of odor problems.
Accordingly, in addition to the above components the invention relates to compositions which may also contain conventional ingredients for such compositions.
Description
~284~7 DETERGENT COMPOSITION
Background of the Invention This invention relates to chlorine-stable detergent compositions containing nonionic surfactants and to a process for the preparation thereof.
Active chlorine containing compounds such as sodium hypochlorite have been widely used for bleaching fabrics, sterilizing in commercial warewashing, and deodo-rizing in hard surfaces cleaners. Because solid compounds particularly sodium hypochlorite are unstable and can decompose violently, they are commonly used as an aqueous solution. However, a sodium hypochlorite solution will decompose slowly over a period of time. Addition of a surfactant generally accelerates this decomposition, resulting in loss of stability and efficacy. While some surfactants with enhanced chlorine stability are known, for example, those disclosed in U.S. 4,071,463 and U.S.
4,174,289 these are all anionic types which are generally high foaming surfactants.
For many applications nonionic surfactants are much more suitable since there are many nonionic surfactants available which are low foaming surfactants. However, heretofore, much difficulty has accompanied the preparation of detergent compositions comprising both an active chlorine-containing compound and a nonionic surfactant ~2134~L7 because of the interaction which generally occurs between the two. This interaction generally results in discolor-ation and degradation of the detergent composition with an accompanying loss in the available chlorine content of the composition. Since a nonionic surfactant possesses wetting properties and an active chlorine compound possesses bleaching, cleaning and sanitizing properties, it is desirable to have both compounds present in detergent compositions.
Several attempts have been made to prepare a detergent composition containing both a chlorine compound and a nonionic surfactant but heretofore all have failed for one reason or another. For example, U.S. 2,895,916 relates to a process for the preparation of detergent compositions containing an active chlorine compound. Disclosed is the use of a nonionic surfactant in the preparation of the ! compositions. It has now been found that although detergent compositions containing an active chlorine compound and a nonionic surfactant may be prepared according to the process of this patent, the compositions are not stable with respect to the active chlorine content; that is, within a very short time the starting available chlorine content decreases to such an extent that for all practical purposes the detergent compositions are chlorine-free.
Accordingly it is a purpose of the instant invention to provide a chlorine stable detergent composition containing nonionic surfactant.
Additional Background Patents Patent No. Issued Inventor(s) Assignee 4,507,219 3/26/85 Hughes P&G
4,438,016 3/20/84 Kiewert Henkel 4,329,247 5/11/82 Parmer PDI Inc.
4,510,067 4/9/85 Ozmeral BASF Wyandotte 3,359207 12/19/67 Kaneko at el BASF Wyandotte Summary of The Invention The instant invention relates to a composition comprising a Bisphenol initiated polyoxyalkylene compound, a chlorine releasing compound and water. This composition has varied uses as a fabric cleaner with bleaching properties, a warewashing composition having sterilization properties and a variety of cleaners having a minimum of odor problems.
Accordingly, in addition to the above components the invention relates to compositions which may also contain conventional ingredients for such compositions.
~2~
Detailed Descri tion of the Preferred Embodiments p The Bisphenol initiated compound employed in the composition of this invention is a cogeneric mixture of conjugated polyoxyalkylene compounds containing in their structure, C3 to C5 oxyalkylene groups, oxyethylene groups and the nucleus of a Bisphenol compound originally con-taining a pair o~ reactive hydrogen atoms. The compounds may be heteric or block and are characterized in that the oxyalkylene groups which are attached to the Bisphenol compound at the site of the reactive hydrogen atoms.
In one preferred embodiment, the C3-C5 oxyalkylene groups are present in chains that are attached to the Bisphenol compound at the site of the reactive hydrogen atoms, therefore constituting a C3-C5 polyoxyalkylene polymer, the oxyethylene groups being attached to the C3-C5 polyoxyalkylene polymer in polyoxyethylene chains. In another preferred embodiment the polyoxyethylene groups are present in polyoxyethylene chains that are attached to the Bisphenol nucleus at the site of the reactive hydrogen atoms thereby constituting a polyoxyethylene polymer; with the C3-C5 oxyalkylene groups being attached to the polyoxy-ethylene polymer in C3-C5 polyoxyalkylene chains. In a third preferred embodiment, the oxyalkylene groups are a heteric mixtures of C3-C5 oxyalkylene groups with oxyethylene groups.
~28'~7 The alkylene oxide compound is prepared by reacting in the presence of a base catalyst a Bisphenol compound with the alkylene oxides. The alkylene oxides may be a mixture or the Bisphenol may be reacted first with one alkylene oxide, then the other, such as for example reaction first with the C3-C5 alkylene oxide followed by reaction with ethylene oxide. The Bisphenol may alternatively be reacted first with ethylene oxide followed by the C3-C5 alkylene oxide depending on which product is desired. The method of preparation of a reaction product of Bisphenol with propylene oxide and ethylene oxide or butylene oxide and ethylene oxide is well known to those skilled in the art and need not be described here.
Bisphenol A is the preferred initiator compound and is well known to those skilled in the art as 4,4'-isopropylidene-diphenol. Bisphenol B may also be employed which is known to those skilled in the art as p,p'-sec-butylidene-diphenol. Any of the conventional catalysts employed for oxyalkylation may be employed such as potassium hydroxide, sodium hydroxide, boron trifluoride dietherate and any metal oxide.
In a preferred embodiment, generally at least a portion of the Bisphenol compound is reacted with a portion of C3-C5 oxide or the ethylene oxide or mixture of both in a conventional manner to produce a Bisphenol component which is a liquid. The amount of said alkylene oxide may range from 1 to 10 moles per mole of Bisphenol compound. This small amount is employed in order to have a liquid in which to carry out the reaction after which additional Bisphenol compound as well as the alkylene oxides may be added to the reaction mixture to produce the final product. The initial reaction mixture contains by weight about 1 to 95 percent of the total amount of Bisphenol component, about 0.1 to 5 percent by weight catalyst and about 1 to 10 moles of alkylene oxide per mole of Bisphenol compound. The mixture is heated to a temperature of from about 100 to 135C.
After stripping for about 15 to 60 minutes at a temperature of about ~5 to 125C at a pressure of less than 10 millimeters of mercury, the vacuum is relieved to about 0 to 5 psig with nitrogen and the remaining alkylene oxides added over a period of about 1 to 12 hours.
The reaction then proceeds until a constant pressure is observed which requires from about one to four hours. As previously stated the ethylene oxide and C3-C5 higher alkylene oxide may be a mixture or may be reacted sequentially with either the higher alkylene oxide added first ~ollowed by the ethylene oxide or vice versa.
The ratios of the alkylene oxides and the Bisphenol component will depend on the ultimate product desired. For purposes of the instant invention, it is preferred to employ ~ 2~
an alkoxylated Bisphenol product having an overall molecular weight of about 1100 to 15,000 preferably about 1900 to 9000 containing about 10 to 90 percent preferably about 10 to 40 percent oxyethylene groups.
The product produced by the reaction of the Bisphenol compound with the alkylene oxides is believed to be a cogeneric mixture of polymers denominated by the following formula H (A)m ~ - C - ~ -0-(A)m-H (I) Wherein A comprises oxyethylene and C3-C5 oxy-alkylene groups to form either a heteric or block copolymer;
m is a whole number selected to give an overall average molecular weight of the product of 1100 to 15,000, preferably 1900 to 9000, and X is CH3 or C2H5.
In a preferred embodiment of the invention, A
comprises a heteric mixture of oxyethylene groups and groups selected from oxypropylene and oxybutylene. In another preferred embodiment the oxyethylene groups are attached to an oxygen that is attached to a phenyl group and the oxypropylene or oxybutylene groups are attached to the opposite ends of the oxyethylene groups. In still another preferred embodiment, A comprises oxyethylene groups and groups selected from oxypropylene and oxybutylene groups wherein said oxypropylene or oxybutylene groups are attached to the oxygen that in turn is attached to a phenyl group and the oxyethylene groups are attached to the opposite end of the oxypropylene or oxybutylene groups. The total molecular weight of the final product is from about 1100 to 15,000 preferably about 1900 to 4000. The percentage of oxyethylene groups in these compounds is from about 10 to 90, preferably about 10 to 40. The preferred oxyalkylated Bisphenol block copolymers employed in the instant invention i5 believed to be a cogeneric mixture of polymers denomi-nated by the following formulas:
H0(C2H40)n(cyH2yo)m ~ ~~~ ~ ~0(CyH2yo)m(c2H4o)nH (II) and H0(CyH2yo)m(c2H4o)n ~ ~ ~ 2 4 n y 2y m ~L~ 7 Wherein x is CH3 or C2H5, y is 3 or 4, m and n are whole numbers selected to give an overall molecular weight from about 1100 to 15,000 preferably about 1900 to 9000, and a percent of oxyethylene groups from about lO to 90, preferably about 10 to 40. The oxybutylene chains option-ally but advantageously contain small amounts of oxyethylene and oxypropylene groups, the oxypropylene chains optionally, but advantageously, contain small amounts of oxyethylene and oxybutylene groups and the oxyethylene chains also option-ally, but advantageously, contain small amounts of oxy-propylene and oxybutylene groups. These compositions are generally described in the U. S. Patents Nos. 2,677,700, 2,674,619, and 2,979,528. The term "cogeneric mixture" used herein is a term that has been coined to designate a series of closely related touching homologues that are obtained by condensing a plurality of alkylene oxide units with a reactive hydrogen compound (see United States Patent 2,549,438, particularly the sections beginning at column 12, line 40). This expression is well known to those skilled in the art as can be seen from U.S. Patents 2,677,700;
2,674,619; and 2,979,528.
Active chlorine containing compounds which may be employed in accordance with the instant invention include ; chlorinated trisodium phosphate, trichlorocyanuric acid, sodium salt of dichlorocyanuric acid, potassium salt of '~L;~ 7 dichlorocyanuric acid, sodium hypochlorite, potassium hypochlorite and 1,3-dichloro-5,5-dimethylhydantoin. The three component composition of the invention which comprises a Bisphenol initiated compound, chlorine releasing compound and water is useful for various cleaning, bleaching and sterilizing applications. Such three component composition to be used as is or mixed with other ingredients comprises from about 1.0 to 15 percent, preferably about 1.0 to 5.0 percent Bisphenol initiated compound, about 1.0 to 10 percent, preferably about 1.0 to 5.0 percent chlorine releasing compound and about 75 to 98 percent, preferably about 90 to 98 percent water.
Normally these three components would be formu-lated with other ingredients or additives depending upon the use of the ultimate product, i.e., whether for cleaning fabrics, for warewashing, for hard surface cleaners or other uses. For purpose of describing the instant invention any other components which might be present with the above three are referred to herein as additives throughout the specifi-cation and claims. The manner of using these components byincorporating in a dishwashing, laundry, hard surface or other detergent composition is well known to those skilled in the art. Such other ingredients include other surfactants, which may be anionic or cationic, builders, bleaches, abrasives, fillers, dyes, perfumes, soil anti-rledeposition agents, optical brighteners, hydrotropes,etc. An important component of cleaning compositions particularly automatic dishwashing detergents are the builders or builder salts such as an alkaline condensed phosphate salt, for instance, tetrasodium pyrophosphate and those polyphosphates of the calcium and magnesium ion sequestering type whose Na20/P205 ratios range from 1:1 to 1.67:1 and 20 to 80 weight percent of an alkaline detergent salt such as sodium carbonate, sodium bicarbonate and mixtures thereof, di- and trisodium orthophosphate, sodium metasilicate, sodium sesquisilicate, borax and sodium borate.
Alternatively to the use of phosphate builders, any of the water-soluble metal salts of citric acid can be used in the practice of the present invention. However, all salts do not serve with equal effectiveness, and the alkali metal salts, particularly the sodium and potassium citrates, are preferred. Suitable proportions of silicates in dishwashing formulations are employed to overcome certain difficulties. The silicate used is preferably solid granular sodium metasilicate, a commercially available material. Sodium silicates in which the mole ratio of SiO2:Na20 are more than 1:1, e.g., 2:1 or 3:1, may be used in place of the sodium metasilicate.
~ Z~ 7 The combination of the citrate and condensed phosphate salt (e.g., sodium tripolyphosphate) appears to result in an enhanced activity.
Preferred over all cleaning compositions will comprise from about 10 to 15 percent preferably about 1.0 to 5.0 percent Bisphenol initiated polyoxyalkylene copolymer, about 1.0 to 10 percent, preferably about 1.0 to 5.0 percent chlorine releasing compound, up to about 60 percent, preferably about 5.0 to 30 percent additives and about 15 to 98 percent, preferably about 40 to 90 percent water. In any event, the ratio of Bisphenol initiated compound to chlorine releasing compound should range from about 1:10 to 10:1 and preferably from about 1:3 to 3:1.
When used for washing purposes in either a dishwashing or laundry solution such solution may contain about 0.1 to 0.5 and preferably about 0.15 to 0.30 percent by weight of the total detergent composition, balance water.
The examples which follow illustrate in more detail the practice of the instant invention. Unless otherwise indicated all temperatures are in degrees Centi-grade and all parts, percentages, etc. are by weight throughout this application and claims.
_b;~ 7 Examples 1-5 Five three-component mixtures were prepared comprising two percent sodium hypochlorite one percent of the surfactant shown in Table I below, balance water. The five formulations were stored at 90F and monitored for available chlorine level each day by ASTM test method.
D2022-64 (Reapproved 1980).
When the percent available chlorine was half the value of the original fresh composition the number of days to reach this point was recorded. This is set forth in Table I below under the column headed "Bleach Half-Life (days)."
TABLE I
Example No. SurfactantBleach Half-Life (days) In the above table nonionic No. 1 is a block copolymer which is a polyoxyethylene adduct of a polyoxypropylene glycol having a central polyoxypropylene chain and polyoxyethylene chains on each end thereof. Such compositions are described in U.S. Patents 2,677,700, 2,674,619 2,979,528 the molecular weight of the polyoxypropylene hydrophobe is about 1750 and the copolymer contains about 10 percent by weight oxyethylene groups.
Surfactant No. 2 is a Bisphenol A initiated polyoxypropylene polyoxyethylene block copolymer of the type shown in formula II above having a molecular weight of the hydrophobe of about 1750, a total molecular weight of about 2000 and containing 10 percent by weight oxyethylene groups.
Surfactant No. 3 is a Bisphenol A initiated polyoxypropylene polyoxyethylene block copolymer of the type shown in formula II above having a molecular weight of the hydrophobe of about 2300, a total molecular weight of about 2~00 and containing 10 percent by weight oxyethylene groups.
Surfactant No. 4 is a Bisphenol A initiated heteric oxyethylene/oxypropylene copolymer of the type shown in formula I above having a total molecular weight of 1800 and an ethylene oxide:propylene oxide weight ratio of 25:75.
Surfactant No. 5 is an anionic surfactant sold under the trademark Dowfax 3B2 which is sodium n-decyl diphenyloxide disulfonate.
The superiority of the Bisphenol A initiated copolymers over the most closely related nonionic copolymer in terms of sodium hypochlorite stability is clearly shown in the above Table. More specifically, surfactant No. 1 and ~2~
surfactant No. 2 are essentially the same nonionic copolymer w:ith the exception that surfactant No. 1 is propylene glycol initiated whereas surfactant No. 2 is a Bisphenol A
initiated copolymer. From the Table it can be seen that the bleach half-life of the Bisphenol A initiated copolymer is more than twice that of the propylene glycol initiated copolymer. Example 3 demonstrates that similar results are obtained with a similar Bisphenol A initiated polyoxy-alkylene block copolymer having a higher molecular weight for the hydrophobe. Example 4 demonstrates that a heteric Bisphenol A polyoxyalkylene copolymer is also e~fective.
Example 5 demonstrates that the Bisphenol A initiated nonionics of the instant invention have a bleach half-life as good or better than the commercial anionic surfactant.
The nonionics have advantages for many purposes over an anionic surfactant and the ones tested are particularly effective in that they are low foaming surfactants.
Example 6 Example 2 is repeated with the exception that the surfactant is a Bisphenol A initiated polyoxyethylene polyoxypropylene block copolymer of the type shown in formula III above. Results similar to Example 2 are obtained.
Example 7 Example 2 is repeated with the exception that the surfactant employed is a Bisphenol A initiated polyoxy-butylene polyoxyethylene block copolymer the type shown in formula II above having a total molecular weight of about 1300 and containing 10 percent by weight oxyethylene groups. Results similar to Example 2 are obtained.
Examples 8 through 13 Six aqueous solutions were prepared consisting of five percent of the surfactant indicated in Table II below, an amount of sodium hypochlorite sufficient to provide three percent available chlorine and one weight percent sodium hydroxide. In addition the composition of Examples 8 and 9 included, respectively, 3.g percent and 3.1 percent of a hydrotrope which was sodium 2-ethylhexyl sulfate sold under the tradename Witcolate D-510. This was added in order to solublize the surfactant, Each of these compositions was stored for 19 days at 105F. The percent chlorine was determined at the end of the 19 days by the method described above for Example 1-5. The percentages of the chlorine in the original composition retained after the 19 days are shown in Table II below.
TABLE II
Percent Chlorine _xample No. Surfactant Retained In the above examples surfactant No. 6 was a propylene glycol initiated polyoxypropylene polyethylene block copolymer having a molecular weight of the polyoxy-propylene hydrophobe of about 1750 and containing 40 percent by weight oxyethylene groups.
Surfactant No. 7 was a Bisphenol A initiated polyoxypropylene polyoxyethylene block copolymer the type shown in formula II above having a molecular weight of the hydrophobe of about 1750, a total molecular weight of about 2900 and containing 40 percent oxyethylene groups.
Surfactant No. 8 was a propylene glycol initiated polyoxypropylene polyoxyethylene block copolymer having a polyoxypropylene hydrophobe molecular weight of about 1750 containing 80 percent by weight oxyethylene groups.
~2~ 7 Surfactant No. 9 was a Bisphenol A initiated polyoxypropylene polyoxyethylene block copolymer of the type shown in formula II sbove having a molecular weight of the hydrophobe of about 1750 a total molecular weight of about 8400 and containing 80 percent by weight oxyethylene groups.
As pointed out above, surfactant No. 1 and surfactant No. 2 differ only in that surfactant No. 1 is a propylene glycol initiated block copolymer and surfactant No. 2 is a Bisphenol A initiated block copolymer. Similarly surfactants Nos. 7 and 9 differ from surfactants Nos. 6 and 8, respectively, only in the different initiator employed, that is to say surfactants 7 and 9 employed Bisphenol A
initiator where as 6 and 8 employ a propylene gLycol initiator. It can be seen from Table II that in each case the Bisphenol A initiated copolymer had a greater percentage chlorine retention than the similar propylene glycol initiated copolymer.
Example 10 A detergent composition is prepared consisting of by weight 9 percent surfactant No. 2, 2.0 percent sodium hypochlorite, 4 percent tetrasodium pyrophosphate, 10 percent linear alkylbenzene sulfonate, and 75 percent water.
A washing solution for laundry purposes is prepared by mixing this detergent composition with water in amount of 0.15 percent by weight of the detergent composi-tion balance water. This washing solution is characterized by low foaming good bleaching and good cleaning properties when used in an automatic washing machine.
Background of the Invention This invention relates to chlorine-stable detergent compositions containing nonionic surfactants and to a process for the preparation thereof.
Active chlorine containing compounds such as sodium hypochlorite have been widely used for bleaching fabrics, sterilizing in commercial warewashing, and deodo-rizing in hard surfaces cleaners. Because solid compounds particularly sodium hypochlorite are unstable and can decompose violently, they are commonly used as an aqueous solution. However, a sodium hypochlorite solution will decompose slowly over a period of time. Addition of a surfactant generally accelerates this decomposition, resulting in loss of stability and efficacy. While some surfactants with enhanced chlorine stability are known, for example, those disclosed in U.S. 4,071,463 and U.S.
4,174,289 these are all anionic types which are generally high foaming surfactants.
For many applications nonionic surfactants are much more suitable since there are many nonionic surfactants available which are low foaming surfactants. However, heretofore, much difficulty has accompanied the preparation of detergent compositions comprising both an active chlorine-containing compound and a nonionic surfactant ~2134~L7 because of the interaction which generally occurs between the two. This interaction generally results in discolor-ation and degradation of the detergent composition with an accompanying loss in the available chlorine content of the composition. Since a nonionic surfactant possesses wetting properties and an active chlorine compound possesses bleaching, cleaning and sanitizing properties, it is desirable to have both compounds present in detergent compositions.
Several attempts have been made to prepare a detergent composition containing both a chlorine compound and a nonionic surfactant but heretofore all have failed for one reason or another. For example, U.S. 2,895,916 relates to a process for the preparation of detergent compositions containing an active chlorine compound. Disclosed is the use of a nonionic surfactant in the preparation of the ! compositions. It has now been found that although detergent compositions containing an active chlorine compound and a nonionic surfactant may be prepared according to the process of this patent, the compositions are not stable with respect to the active chlorine content; that is, within a very short time the starting available chlorine content decreases to such an extent that for all practical purposes the detergent compositions are chlorine-free.
Accordingly it is a purpose of the instant invention to provide a chlorine stable detergent composition containing nonionic surfactant.
Additional Background Patents Patent No. Issued Inventor(s) Assignee 4,507,219 3/26/85 Hughes P&G
4,438,016 3/20/84 Kiewert Henkel 4,329,247 5/11/82 Parmer PDI Inc.
4,510,067 4/9/85 Ozmeral BASF Wyandotte 3,359207 12/19/67 Kaneko at el BASF Wyandotte Summary of The Invention The instant invention relates to a composition comprising a Bisphenol initiated polyoxyalkylene compound, a chlorine releasing compound and water. This composition has varied uses as a fabric cleaner with bleaching properties, a warewashing composition having sterilization properties and a variety of cleaners having a minimum of odor problems.
Accordingly, in addition to the above components the invention relates to compositions which may also contain conventional ingredients for such compositions.
~2~
Detailed Descri tion of the Preferred Embodiments p The Bisphenol initiated compound employed in the composition of this invention is a cogeneric mixture of conjugated polyoxyalkylene compounds containing in their structure, C3 to C5 oxyalkylene groups, oxyethylene groups and the nucleus of a Bisphenol compound originally con-taining a pair o~ reactive hydrogen atoms. The compounds may be heteric or block and are characterized in that the oxyalkylene groups which are attached to the Bisphenol compound at the site of the reactive hydrogen atoms.
In one preferred embodiment, the C3-C5 oxyalkylene groups are present in chains that are attached to the Bisphenol compound at the site of the reactive hydrogen atoms, therefore constituting a C3-C5 polyoxyalkylene polymer, the oxyethylene groups being attached to the C3-C5 polyoxyalkylene polymer in polyoxyethylene chains. In another preferred embodiment the polyoxyethylene groups are present in polyoxyethylene chains that are attached to the Bisphenol nucleus at the site of the reactive hydrogen atoms thereby constituting a polyoxyethylene polymer; with the C3-C5 oxyalkylene groups being attached to the polyoxy-ethylene polymer in C3-C5 polyoxyalkylene chains. In a third preferred embodiment, the oxyalkylene groups are a heteric mixtures of C3-C5 oxyalkylene groups with oxyethylene groups.
~28'~7 The alkylene oxide compound is prepared by reacting in the presence of a base catalyst a Bisphenol compound with the alkylene oxides. The alkylene oxides may be a mixture or the Bisphenol may be reacted first with one alkylene oxide, then the other, such as for example reaction first with the C3-C5 alkylene oxide followed by reaction with ethylene oxide. The Bisphenol may alternatively be reacted first with ethylene oxide followed by the C3-C5 alkylene oxide depending on which product is desired. The method of preparation of a reaction product of Bisphenol with propylene oxide and ethylene oxide or butylene oxide and ethylene oxide is well known to those skilled in the art and need not be described here.
Bisphenol A is the preferred initiator compound and is well known to those skilled in the art as 4,4'-isopropylidene-diphenol. Bisphenol B may also be employed which is known to those skilled in the art as p,p'-sec-butylidene-diphenol. Any of the conventional catalysts employed for oxyalkylation may be employed such as potassium hydroxide, sodium hydroxide, boron trifluoride dietherate and any metal oxide.
In a preferred embodiment, generally at least a portion of the Bisphenol compound is reacted with a portion of C3-C5 oxide or the ethylene oxide or mixture of both in a conventional manner to produce a Bisphenol component which is a liquid. The amount of said alkylene oxide may range from 1 to 10 moles per mole of Bisphenol compound. This small amount is employed in order to have a liquid in which to carry out the reaction after which additional Bisphenol compound as well as the alkylene oxides may be added to the reaction mixture to produce the final product. The initial reaction mixture contains by weight about 1 to 95 percent of the total amount of Bisphenol component, about 0.1 to 5 percent by weight catalyst and about 1 to 10 moles of alkylene oxide per mole of Bisphenol compound. The mixture is heated to a temperature of from about 100 to 135C.
After stripping for about 15 to 60 minutes at a temperature of about ~5 to 125C at a pressure of less than 10 millimeters of mercury, the vacuum is relieved to about 0 to 5 psig with nitrogen and the remaining alkylene oxides added over a period of about 1 to 12 hours.
The reaction then proceeds until a constant pressure is observed which requires from about one to four hours. As previously stated the ethylene oxide and C3-C5 higher alkylene oxide may be a mixture or may be reacted sequentially with either the higher alkylene oxide added first ~ollowed by the ethylene oxide or vice versa.
The ratios of the alkylene oxides and the Bisphenol component will depend on the ultimate product desired. For purposes of the instant invention, it is preferred to employ ~ 2~
an alkoxylated Bisphenol product having an overall molecular weight of about 1100 to 15,000 preferably about 1900 to 9000 containing about 10 to 90 percent preferably about 10 to 40 percent oxyethylene groups.
The product produced by the reaction of the Bisphenol compound with the alkylene oxides is believed to be a cogeneric mixture of polymers denominated by the following formula H (A)m ~ - C - ~ -0-(A)m-H (I) Wherein A comprises oxyethylene and C3-C5 oxy-alkylene groups to form either a heteric or block copolymer;
m is a whole number selected to give an overall average molecular weight of the product of 1100 to 15,000, preferably 1900 to 9000, and X is CH3 or C2H5.
In a preferred embodiment of the invention, A
comprises a heteric mixture of oxyethylene groups and groups selected from oxypropylene and oxybutylene. In another preferred embodiment the oxyethylene groups are attached to an oxygen that is attached to a phenyl group and the oxypropylene or oxybutylene groups are attached to the opposite ends of the oxyethylene groups. In still another preferred embodiment, A comprises oxyethylene groups and groups selected from oxypropylene and oxybutylene groups wherein said oxypropylene or oxybutylene groups are attached to the oxygen that in turn is attached to a phenyl group and the oxyethylene groups are attached to the opposite end of the oxypropylene or oxybutylene groups. The total molecular weight of the final product is from about 1100 to 15,000 preferably about 1900 to 4000. The percentage of oxyethylene groups in these compounds is from about 10 to 90, preferably about 10 to 40. The preferred oxyalkylated Bisphenol block copolymers employed in the instant invention i5 believed to be a cogeneric mixture of polymers denomi-nated by the following formulas:
H0(C2H40)n(cyH2yo)m ~ ~~~ ~ ~0(CyH2yo)m(c2H4o)nH (II) and H0(CyH2yo)m(c2H4o)n ~ ~ ~ 2 4 n y 2y m ~L~ 7 Wherein x is CH3 or C2H5, y is 3 or 4, m and n are whole numbers selected to give an overall molecular weight from about 1100 to 15,000 preferably about 1900 to 9000, and a percent of oxyethylene groups from about lO to 90, preferably about 10 to 40. The oxybutylene chains option-ally but advantageously contain small amounts of oxyethylene and oxypropylene groups, the oxypropylene chains optionally, but advantageously, contain small amounts of oxyethylene and oxybutylene groups and the oxyethylene chains also option-ally, but advantageously, contain small amounts of oxy-propylene and oxybutylene groups. These compositions are generally described in the U. S. Patents Nos. 2,677,700, 2,674,619, and 2,979,528. The term "cogeneric mixture" used herein is a term that has been coined to designate a series of closely related touching homologues that are obtained by condensing a plurality of alkylene oxide units with a reactive hydrogen compound (see United States Patent 2,549,438, particularly the sections beginning at column 12, line 40). This expression is well known to those skilled in the art as can be seen from U.S. Patents 2,677,700;
2,674,619; and 2,979,528.
Active chlorine containing compounds which may be employed in accordance with the instant invention include ; chlorinated trisodium phosphate, trichlorocyanuric acid, sodium salt of dichlorocyanuric acid, potassium salt of '~L;~ 7 dichlorocyanuric acid, sodium hypochlorite, potassium hypochlorite and 1,3-dichloro-5,5-dimethylhydantoin. The three component composition of the invention which comprises a Bisphenol initiated compound, chlorine releasing compound and water is useful for various cleaning, bleaching and sterilizing applications. Such three component composition to be used as is or mixed with other ingredients comprises from about 1.0 to 15 percent, preferably about 1.0 to 5.0 percent Bisphenol initiated compound, about 1.0 to 10 percent, preferably about 1.0 to 5.0 percent chlorine releasing compound and about 75 to 98 percent, preferably about 90 to 98 percent water.
Normally these three components would be formu-lated with other ingredients or additives depending upon the use of the ultimate product, i.e., whether for cleaning fabrics, for warewashing, for hard surface cleaners or other uses. For purpose of describing the instant invention any other components which might be present with the above three are referred to herein as additives throughout the specifi-cation and claims. The manner of using these components byincorporating in a dishwashing, laundry, hard surface or other detergent composition is well known to those skilled in the art. Such other ingredients include other surfactants, which may be anionic or cationic, builders, bleaches, abrasives, fillers, dyes, perfumes, soil anti-rledeposition agents, optical brighteners, hydrotropes,etc. An important component of cleaning compositions particularly automatic dishwashing detergents are the builders or builder salts such as an alkaline condensed phosphate salt, for instance, tetrasodium pyrophosphate and those polyphosphates of the calcium and magnesium ion sequestering type whose Na20/P205 ratios range from 1:1 to 1.67:1 and 20 to 80 weight percent of an alkaline detergent salt such as sodium carbonate, sodium bicarbonate and mixtures thereof, di- and trisodium orthophosphate, sodium metasilicate, sodium sesquisilicate, borax and sodium borate.
Alternatively to the use of phosphate builders, any of the water-soluble metal salts of citric acid can be used in the practice of the present invention. However, all salts do not serve with equal effectiveness, and the alkali metal salts, particularly the sodium and potassium citrates, are preferred. Suitable proportions of silicates in dishwashing formulations are employed to overcome certain difficulties. The silicate used is preferably solid granular sodium metasilicate, a commercially available material. Sodium silicates in which the mole ratio of SiO2:Na20 are more than 1:1, e.g., 2:1 or 3:1, may be used in place of the sodium metasilicate.
~ Z~ 7 The combination of the citrate and condensed phosphate salt (e.g., sodium tripolyphosphate) appears to result in an enhanced activity.
Preferred over all cleaning compositions will comprise from about 10 to 15 percent preferably about 1.0 to 5.0 percent Bisphenol initiated polyoxyalkylene copolymer, about 1.0 to 10 percent, preferably about 1.0 to 5.0 percent chlorine releasing compound, up to about 60 percent, preferably about 5.0 to 30 percent additives and about 15 to 98 percent, preferably about 40 to 90 percent water. In any event, the ratio of Bisphenol initiated compound to chlorine releasing compound should range from about 1:10 to 10:1 and preferably from about 1:3 to 3:1.
When used for washing purposes in either a dishwashing or laundry solution such solution may contain about 0.1 to 0.5 and preferably about 0.15 to 0.30 percent by weight of the total detergent composition, balance water.
The examples which follow illustrate in more detail the practice of the instant invention. Unless otherwise indicated all temperatures are in degrees Centi-grade and all parts, percentages, etc. are by weight throughout this application and claims.
_b;~ 7 Examples 1-5 Five three-component mixtures were prepared comprising two percent sodium hypochlorite one percent of the surfactant shown in Table I below, balance water. The five formulations were stored at 90F and monitored for available chlorine level each day by ASTM test method.
D2022-64 (Reapproved 1980).
When the percent available chlorine was half the value of the original fresh composition the number of days to reach this point was recorded. This is set forth in Table I below under the column headed "Bleach Half-Life (days)."
TABLE I
Example No. SurfactantBleach Half-Life (days) In the above table nonionic No. 1 is a block copolymer which is a polyoxyethylene adduct of a polyoxypropylene glycol having a central polyoxypropylene chain and polyoxyethylene chains on each end thereof. Such compositions are described in U.S. Patents 2,677,700, 2,674,619 2,979,528 the molecular weight of the polyoxypropylene hydrophobe is about 1750 and the copolymer contains about 10 percent by weight oxyethylene groups.
Surfactant No. 2 is a Bisphenol A initiated polyoxypropylene polyoxyethylene block copolymer of the type shown in formula II above having a molecular weight of the hydrophobe of about 1750, a total molecular weight of about 2000 and containing 10 percent by weight oxyethylene groups.
Surfactant No. 3 is a Bisphenol A initiated polyoxypropylene polyoxyethylene block copolymer of the type shown in formula II above having a molecular weight of the hydrophobe of about 2300, a total molecular weight of about 2~00 and containing 10 percent by weight oxyethylene groups.
Surfactant No. 4 is a Bisphenol A initiated heteric oxyethylene/oxypropylene copolymer of the type shown in formula I above having a total molecular weight of 1800 and an ethylene oxide:propylene oxide weight ratio of 25:75.
Surfactant No. 5 is an anionic surfactant sold under the trademark Dowfax 3B2 which is sodium n-decyl diphenyloxide disulfonate.
The superiority of the Bisphenol A initiated copolymers over the most closely related nonionic copolymer in terms of sodium hypochlorite stability is clearly shown in the above Table. More specifically, surfactant No. 1 and ~2~
surfactant No. 2 are essentially the same nonionic copolymer w:ith the exception that surfactant No. 1 is propylene glycol initiated whereas surfactant No. 2 is a Bisphenol A
initiated copolymer. From the Table it can be seen that the bleach half-life of the Bisphenol A initiated copolymer is more than twice that of the propylene glycol initiated copolymer. Example 3 demonstrates that similar results are obtained with a similar Bisphenol A initiated polyoxy-alkylene block copolymer having a higher molecular weight for the hydrophobe. Example 4 demonstrates that a heteric Bisphenol A polyoxyalkylene copolymer is also e~fective.
Example 5 demonstrates that the Bisphenol A initiated nonionics of the instant invention have a bleach half-life as good or better than the commercial anionic surfactant.
The nonionics have advantages for many purposes over an anionic surfactant and the ones tested are particularly effective in that they are low foaming surfactants.
Example 6 Example 2 is repeated with the exception that the surfactant is a Bisphenol A initiated polyoxyethylene polyoxypropylene block copolymer of the type shown in formula III above. Results similar to Example 2 are obtained.
Example 7 Example 2 is repeated with the exception that the surfactant employed is a Bisphenol A initiated polyoxy-butylene polyoxyethylene block copolymer the type shown in formula II above having a total molecular weight of about 1300 and containing 10 percent by weight oxyethylene groups. Results similar to Example 2 are obtained.
Examples 8 through 13 Six aqueous solutions were prepared consisting of five percent of the surfactant indicated in Table II below, an amount of sodium hypochlorite sufficient to provide three percent available chlorine and one weight percent sodium hydroxide. In addition the composition of Examples 8 and 9 included, respectively, 3.g percent and 3.1 percent of a hydrotrope which was sodium 2-ethylhexyl sulfate sold under the tradename Witcolate D-510. This was added in order to solublize the surfactant, Each of these compositions was stored for 19 days at 105F. The percent chlorine was determined at the end of the 19 days by the method described above for Example 1-5. The percentages of the chlorine in the original composition retained after the 19 days are shown in Table II below.
TABLE II
Percent Chlorine _xample No. Surfactant Retained In the above examples surfactant No. 6 was a propylene glycol initiated polyoxypropylene polyethylene block copolymer having a molecular weight of the polyoxy-propylene hydrophobe of about 1750 and containing 40 percent by weight oxyethylene groups.
Surfactant No. 7 was a Bisphenol A initiated polyoxypropylene polyoxyethylene block copolymer the type shown in formula II above having a molecular weight of the hydrophobe of about 1750, a total molecular weight of about 2900 and containing 40 percent oxyethylene groups.
Surfactant No. 8 was a propylene glycol initiated polyoxypropylene polyoxyethylene block copolymer having a polyoxypropylene hydrophobe molecular weight of about 1750 containing 80 percent by weight oxyethylene groups.
~2~ 7 Surfactant No. 9 was a Bisphenol A initiated polyoxypropylene polyoxyethylene block copolymer of the type shown in formula II sbove having a molecular weight of the hydrophobe of about 1750 a total molecular weight of about 8400 and containing 80 percent by weight oxyethylene groups.
As pointed out above, surfactant No. 1 and surfactant No. 2 differ only in that surfactant No. 1 is a propylene glycol initiated block copolymer and surfactant No. 2 is a Bisphenol A initiated block copolymer. Similarly surfactants Nos. 7 and 9 differ from surfactants Nos. 6 and 8, respectively, only in the different initiator employed, that is to say surfactants 7 and 9 employed Bisphenol A
initiator where as 6 and 8 employ a propylene gLycol initiator. It can be seen from Table II that in each case the Bisphenol A initiated copolymer had a greater percentage chlorine retention than the similar propylene glycol initiated copolymer.
Example 10 A detergent composition is prepared consisting of by weight 9 percent surfactant No. 2, 2.0 percent sodium hypochlorite, 4 percent tetrasodium pyrophosphate, 10 percent linear alkylbenzene sulfonate, and 75 percent water.
A washing solution for laundry purposes is prepared by mixing this detergent composition with water in amount of 0.15 percent by weight of the detergent composi-tion balance water. This washing solution is characterized by low foaming good bleaching and good cleaning properties when used in an automatic washing machine.
Claims (24)
1. A composition of matter comprising water, a chlorine releasing compound, an oxyalkylene compound which is a cogeneric mixture of conjugated polyoxyalkylene compounds containing in their structure C3 - C5 oxyalkylene groups, oxyethylene groups and the nucleus of a Bisphenol compound containing a plurality of reactive hydrogen atoms.
2. The composition of claim 1 wherein said C3 to C5 oxyalkylene groups are oxypropylene groups.
3. The composition of claim 1 wherein said C3 to C5 oxyalkylene groups are oxybutylene groups.
4. The composition of claim 1 comprising about 1.0 to 15 percent of said oxyalkylene compound about 1.0 to 10 percent of said chlorine releasing compound and about 75 to 98 percent water.
5. The composition of claim 4 wherein said C3 to C5 oxyalkylene groups are oxyethylene groups.
6. The composition of claim 4 wherein said C3 to C5 oxyalkylene groups are oxybutylene groups.
7. The composition of claim 4 wherein said Bisphenol initiated compound contains in its structure oxyethylene groups and groups selected from oxybutylene and oxypropylene groups and a nucleus of Bisphenol A containing a plurality of reactive hydrogen atoms; the compounds being characterized in that the oxybutylene or oxypropylene groups are present in chains that are attached to the Bisphenol A
nucleus at the site of the reactive hydrogen atoms; the oxyethylene groups being attached to the polyoxybutylene or polyoxypropylene groups at the end opposite the end of said latter groups which are attached to the Bisphenol A nucleus.
nucleus at the site of the reactive hydrogen atoms; the oxyethylene groups being attached to the polyoxybutylene or polyoxypropylene groups at the end opposite the end of said latter groups which are attached to the Bisphenol A nucleus.
8. The composition of claim 4 wherein said Bisphenol initiated compound contains in its structure oxyethylene groups and groups selected from oxybutylene and oxypropylene groups, and a nucleus of Bisphenol A containing a plurality of reactive hydrogen atoms; the compounds being characterized in that all of the oxyethylene groups are present in polyoxyethylene chains that are attached to the Bisphenol A nucleus at the site of the reactive hydrogen atoms; the oxybutylene or oxypropylene groups being attached to the oxyethylene groups at the end opposite the end of said oxyethylene groups which are attached to the Bisphenol A nucleus.
9. The composition of claim 4 wherein the oxyalkylene groups are a heteric mixture of C3 - C5 oxyalkylene groups with oxyethylene groups.
10. The composition of claim 4 comprising about 1.0 to 15 percent of said oxyalkylene compound about 1.0 to 10 percent of said chlorine releasing compound 0 to about 60 percent conventional additives and about 15 to 98 percent water.
11. The composition of claim 10 wherein said C3 - C5 oxyalkylene groups are oxypropylene groups.
12. The composition of claim 10 wherein said C3 - C5 oxyalkylene groups are oxybutylene groups.
13. The composition of claim 11 wherein said chlorine releasing compound in sodium hypochlorite.
14. The composition of claim 12 wherein said chlorine releasing compound is sodium hypochlorite.
15. The composition of claim 10 wherein said Bisphenol initiated compound contains in its structure oxyethylene groups and groups selected from oxybutylene and oxypropylene groups and a nucleus of Bisphenol A containing a plurality of reactive hydrogen atoms; the compounds being characterized in that all of the oxybutylene or oxypropylene groups are present in chains that are attached to the Bisphenol A nucleus at the site of the reactive hydrogen atoms; the oxyethylene groups being attached to the polyoxy-butylene or polyoxypropylene groups at the end opposite the end of said latter groups which are attached to the Bisphenol A nucleus.
16. The composition of claim 15 wherein said chlorine releasing compound is sodium hypochlorite.
17. The composition of claim 10 wherein said Bisphenol initiated compound contains in its structure oxyethylene groups, groups selected from oxybutylene or oxypropylene groups, and a nucleus of Bisphenol A containing a plurality of reactive hydrogen atoms; the compounds being characterized in that all of the oxyethylene groups are present in polyoxyethylene chains that are attached to the Bisphenol A nucleus at the site of the reactive hydrogen atoms; the oxybutylene or oxypropylene groups being attached to the oxyethylene groups at the end opposite the end of said oxyethylene groups which are attached to the Bisphenol A nucleus.
18. The composition of claim 17 wherein said chlorine releasing compound is sodium hypochlorite.
19. The composition of claim 17 wherein the oxyalkylene groups are heteric mixture of oxyethylene groups with C3 - C5 oxyalkylene groups.
20. The composition of claim 19 wherein said chlorine releasing compound is sodium hypochlorite.
21. A washing solution comprising about 0.1 to 0.5 percent of the composition of claim 10 balance water.
22. The washing solution of claim 21 wherein said C3 to C5 oxyalkylene groups are oxypropylene groups.
23. The washing solution of claim 21 wherein said C3 to C5 oxyalkylene groups are oxybutylene groups.
24
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/800,797 US4661279A (en) | 1985-11-22 | 1985-11-22 | Detergent composition |
| US800,797 | 1991-11-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1284447C true CA1284447C (en) | 1991-05-28 |
Family
ID=25179386
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000522094A Expired - Fee Related CA1284447C (en) | 1985-11-22 | 1986-11-04 | Chlorine stable detergent compositions containing non-ionic surfactants |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US4661279A (en) |
| CA (1) | CA1284447C (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2219596A (en) * | 1988-06-09 | 1989-12-13 | Procter & Gamble | Liquid automatic dishwashing compositions having enhanced stability |
| US5073286A (en) * | 1989-11-20 | 1991-12-17 | Basf Corporation | Stable alkyl and/or aryl silyl ether capped polyether surfactants for liquid cleaning agents containing hypohalite bleaches |
| ES2106068T3 (en) * | 1990-06-11 | 1997-11-01 | Ciba Geigy Ag | AQUEOUS, NON-SILICONED TEXTILE AUXILIARIES, WHICH GENERATE LITTLE FOAM, OBTAINING AND USE THEM. |
| DE10029696A1 (en) | 2000-06-16 | 2001-12-20 | Basf Ag | Washing composition for cleaning fabrics while preventing dye transfer contains water-soluble or -dispersible block copolymer and non-polymeric surfactant |
| US6387864B1 (en) | 2000-12-15 | 2002-05-14 | Ecolab Inc. | Composition and method for prevention of discoloration of detergents using nonionic surfactants and an alkaline source |
| JP6667338B2 (en) * | 2016-03-29 | 2020-03-18 | ライオン株式会社 | Liquid bleach composition |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3172861A (en) * | 1965-03-09 | Hypochlorite bleaching compositions | ||
| US2723241A (en) * | 1952-08-18 | 1955-11-08 | Petrolite Corp | Process for breaking petroleum emulsions |
| JPS4523540Y1 (en) * | 1966-10-24 | 1970-09-17 | ||
| JPS6031239B2 (en) * | 1977-12-23 | 1985-07-20 | 日本ペイント株式会社 | Degreasing cleaning agent |
| DE3130609A1 (en) * | 1981-08-01 | 1983-03-24 | Hoechst Ag, 6000 Frankfurt | DISPERSING AGENTS, METHOD FOR THE PRODUCTION AND USE THEREOF |
| JPS5914986A (en) * | 1982-07-16 | 1984-01-25 | Toyo Ink Mfg Co Ltd | Desensitizing agent |
| US4470914A (en) * | 1982-11-15 | 1984-09-11 | Basf Wyandotte Corporation | Polyoxyalkylene lubricants of improved oxidative stability and lower viscosity |
-
1985
- 1985-11-22 US US06/800,797 patent/US4661279A/en not_active Expired - Lifetime
-
1986
- 1986-11-04 CA CA000522094A patent/CA1284447C/en not_active Expired - Fee Related
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| Publication number | Publication date |
|---|---|
| US4661279A (en) | 1987-04-28 |
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