|Publication number||US3915882 A|
|Publication date||Oct 28, 1975|
|Filing date||Nov 10, 1972|
|Priority date||Nov 10, 1972|
|Also published as||CA1015508A, CA1015508A1, USB305417|
|Publication number||US 3915882 A, US 3915882A, US-A-3915882, US3915882 A, US3915882A|
|Inventors||Joseph Peter Nirschl, Robert Andrew Gloss|
|Original Assignee||Procter & Gamble|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (2), Referenced by (28), Classifications (43)|
|External Links: USPTO, USPTO Assignment, Espacenet|
' United States Patent Nirschl et al.
SOAP COMPOSITIONS Inventors: Joseph Peter Nirschl; Robert Andrew Gloss, both of Cincinnati, Ohio Assignee: The Procter & Gamble Company,
Cincinnati, Ohio Filed: Nov. 10, 1972 Appl. No.: 305,417
Published under the Trial Voluntary Protest Program on January 28, 1975 as document no. B 305,417.
References Cited UNITED STATES PATENTS 2/1973 Kolsky et a1. 252/120 X Oct. 28, 1975 3,765,911 10/1973 Knowles et al. 252/131 X Primary Examiner-Leland A. Sebastian Attorney, Agent, or FirmRichard C. Witte; Thomas H. OFlaherty; Jack D. Schaeffer  ABSTRACT Granular laundering compositions comprising a curd-dispersant-containing soap-based granule, a smectite-type clay and a quaternary ammonium antistatic agent. The soap and curd dispersant are formulated in the granule and the clay is attached to the surface of the granule. The quaternary ammonium compound is formulated in releasable combination with the granule. The resulting compositions enhanced solubility and provide through-the-wash fabric softening and anti-static benefits.
10 Claims, N0 Drawings SOAP COMPOSITIONS BACKGROUND OF THE INVENTION The instant invention relates to granular laundering compositions which provide simultaneous laundering, softening and anti-static benefits on textiles during conventional fabric laundering operations. Such compositions employ a combination of a soap and a curd dispersant in granular form, certain smectite clay compounds having particular cation exchange characteristics, and certain cationic anti-static agents.
Laundry soaps, i.e., the water-soluble salts of fatty acids, provide the user with good fabric cleansing coupled with product mildness. In addition, soaps deposit on many types of fabrics in the form of a curd and thereby provide desirable softening benefits. However, the buildup of heavy soap curd on fabrics eventually results in loss of fabric brightness. Furthermore, soap curd has been found to interfere with the flame retardant finishes commonly applied to childrens clothing. That is to say, flame retardant fabrics coated with a heavy soap curd exhibit decreased levels of flame retardancy which, on removal of the soap curd, are restored to their original level.
From the foregoing, it can be seen that the use of soap-based laundering products presents a dilemma. The soap provides desirable fabric cleaning and through-the-wash fabric softening, but can eventually detract from fabric appearance and decrease the efficacy of the flame retardant finishes present on modern fabrics.
One method for preventing curd buildup on fabrics laundered with soap is to include a curd dispersant in the laundering bath. While this method achieves the desired result, the laundered fabrics no longer have the desirable softening benefits imparted by soap. More importantly, granular laundering compositions which contain both soap and significant amounts of curd dispersant are difficult to dissolve in aqueous laundering baths. When such products are added to water, the soap tends to undergo a phase transition and agglomerates as a gelatinous material which then deposits in an unsightly manner on the fabrics being laundered.
As more fully disclosed in the co-pending application of Ohren, Ser. No. 279,127 filed Aug. 9, 1972, certain smectite-type clay materials can be attached to the surface of soap-based detergent granules containing certain curd dispersants to substantially enhance the solu bility of the granules. Furthermore, once the granules have dissolved, the clay is dispersed throughout the laundry liquor and deposits on the fabric surfaces to provide softening. Thus, the problem of excess curd buildup on fabrics is solved without losing the desirable softening benefits of soap-based compositions.
However, such clay-plus-soap granules, while effective for their intended purpose, do no impart desirable antistatic benefits to fabrics laundered therein. That is to say, commercially acceptable fabric softeners also provide anti-static benefits, and such benefits have come to be expected by the user of such products. The present invention discloses a means for providing these desirable anti-static benefits.
Various clay materials have been utilized in many different types of detergent systems for widely diverse purposes. Clays, for example, have been disclosed for use as builders (Schwartz and Perry, Surface Active Agents, lntersicence Publishers, lnc., 1949, p. 233 and Schwartz, Perry and Berch, Surface Active Agents and Detergents, Vol. II Interscience Publishers, lnc., 1958, pp. 297-300); as watersofteners (British Pat. No. 461,221); as anti-caking agents (U.S. Pat. Nos. 2,625,513 and 2,770,600); as suspending agents (U.S. Pat. Nos. 2,594,257, 2,594,258 and 2,920,045); and as fillers (U.S. Pat. No. 2,708,185).
It is also well known that some clay materials can be deposited on fabrics to impart softening properties thereto. Such clay deposition is usually realized by contacting fabrics to be so treated with aqueous clay suspensions (see, for example, US. Pat. Nos. 3,033,699 and 3,594,221 The co-pending application of Storm and Nirschl, Ser. No. 271,943, filed July 14, 1972, now abandoned, teaches the use of clays as softeners in detergent compositions.
Various quaternary ammonium compounds are known in the art which possess anti-static properties, and the use of clays in combination with conventional cationic agents for various purposes has been taught in the prior art. For example, US. Pat. No. 3,594,212 teaches that quaternary ammonium compounds affixed to the surface of clay can enhance clay deposition on fabrics; see, also, US. Pat. No. 3,625,505. However, as will be seen hereinafter, when quaternary compounds are chemically affixed to clay surfaces in the manner disclosed in the prior art, the desirable anti-static benefits are substantially lost. Furthermore, quaternary ammonium compounds are not generally taught to be useful in combination with anionic materials such as soap in the manner disclosed herein.
While the use of clays as fabric softeners is described in the cited art, such clay softeners are not entirely suitable for this purpose since they do not possess antistatic properties. Indeed, fabrics coated with clays, while exhibiting a soft hand, tend to develop higher levels of static change than the uncoated fabrics, themselves.
The concurrently filed application of Nirschl and Gloss, entitled Detergent Compositions; Ser. No. 305,416, filed Nov. 10, 1972 discloses the use of clayplus-quat softeners and anti-static agents in built, nonsoap detergent compositions.
US. Pat. No. 2,819,228 discloses the use of clays in combination with cationic surfactants as dry emulsifiers; however, these compositions do not contain detergent compounds suitable for laundering fabrics.
It has been heretofore unrecognized that clay minerals of the type used in the present invention can be attached to the surface of soap-based detergent granules, especially those containing curd dispersants, and combined with specific quaternary ammonium compounds to provide soluble soap granules having combined fabric softening and anti-static benefits.
Accordingly, it is an object of the present invention to provide compositions which can be employed to achieve concurrent fabric laundering, fabric softening, and anti-static effects without interfering with flame retardancy.
It is a further object of the present invention to provide soap-based laundering, softening and anti-static compositions containing curd dispersants in the form of granular formulations which can be easily dissolved in water over a wide temperature range.
These and other objects ae obtained herein, as will be seen from the following disclosure.
SUMMARY OF THE INVENTION The present invention encompasses fabric laundering compositions comprising: (A) a granular particle which comprises; (i) from about 30% to about 80% by weight of said particle of a soap compound; and (ii) from about 1% to about 30% by weight of said granular particle of a curd-dispersing agent; (B) an impalpable smectite-type clay having an ion exchange capacity of at least about 50 meq/ 100 g. of clay, attached to the surface of said granular particle; and (C) from about 0.5% to about 15% by weight of a substantially waterinsoluble quaternary ammonium anti-static agent of the formula wherein each R is a hydrocarbyl group containing from about to about 22 carbon atoms and each R is a hydrocarbyl group containing from 1 to about 4 carbon atoms, and wherein X is an anion, i.e., halide, hydroxide, carbonate, phosphate, etc. In the above formula, the integer, n, indicates the charge on the anion; n can be 1 to 3 in the compounds herein. The compositions have a weight ratio of granular particles to smectite clay in the range of from about 20:1 to about 3:1. The weight ratio of smectite-type clay-to-quaternary ammonium compound in the compositions herein is from about 40:1 to about 1:1, preferably about 5:1. The quaternary ammonium compound is present in releasable combination with the compositions herein. By releasable combination is meant that, on admixture with water, the soluble components of the composition granules dissolve and the clay and quaternary compounds are independently suspended in the aqueous medium.
The compositions herein preferably provide a solution pH of from about 6 to about 1 1 when dissolved in water at a concentration of about 0.12% by weight.
In a method aspect, the invention encompasses methods for concurrently cleansing, softening and providing anti-static effects on fibers and fabrics comprising laundering said fabrics in an aqueous laundry bath containing an effective amount (e.g., from about 0.02% to about 2% by weight) of a laundry composition as described above.
DETAILED DESCRIPTION OF THE INVENTION The compositions and processes of this invention employ three essential ingredients: the soap-based granule; the clay; and the quaternary ammonium anti-static agent. The soap granule dissolves and functions in standard fashion to remove soil from fabrics being laun- Anti-Static Agent The quaternary ammonium antistatic agents are em ployed in the instant compositions at-a concentration of from about 0.5% to about preferably from about 0.5% to about 5% by weight, and are therefore.
present in the laundering liquors at levels from about 5 ppm to about ppm. In general, the quaternary anti-stats are used at a clay to quaternary weight ratio of from about 40:1 to about 1:1, preferably about 5:1.
The anti-static agents of this invention are quaternary ammonium salts of the formula wherein each R group is a hydrocarbyl (i.e., alkyl or alkenyl) group containing from about 10 to about 22 carbon atoms and each R group is a short-chain hydrocarbyl group containing from 1 to about 4 carbon atoms. X in the above compounds can be any saltforming anion, e.g., halide, hydroxide ion, sulfat, carbonate, phosphate, etc. The charge on the anion is designated an n, wherein n is 1-3. The number of cationic ammonium groups, n, will equal the change, n, on the anion to provide electrical neutrality. Quaternary ammonium compounds wherein n=1 are commercially available and are preferred herein for this reason.
The quaternary ammonium anti-static agents herein are characterized by their limited solubility in water. That is to say, such quaternary salts are essentially insoluble in water, existing therein in what appears to be the mesomorphic liquid crystalline state. The insolubility of the quaternary salts used herein is a critical aspect of this invention inasmuch as water-soluble quaternary salts become chemically affixed to the surface of the clay,or react with the soap or curd dispersant. When the quaternary anti-static agent is affixed to the surface of the clay, or has reacted with the soap or curd dispersant, it does not perform the desired anti-static function.
The cause of the solubility properties of the particular class of quatemaries found to be useful herein is not known with certainty. While not intending to be limited by theory, it appears that the two extended hydrocarbyl chains c,,' c present in the molecules serve to lower their solubility and probably account for their existence as liquid crystals. In any event, it has now been found the di-long chain quaternaries can be used in releasable combination with compositions containing clays. That is to say, the quaternary compound and the clay are independently suspended in the washing liquor and the quaternary compound does not appear to substantially affix itself to the clay surface by an ion exchange mechanism.
Quaternary ammonium compounds are not generally considered to be useful in combination with anionic materials such as soaps since the opposite charges on these two types of materials cause them to react and precipitate from solution. Surprisingly, it has now been found that the desirable anti-static benefits of the insoluble quaternary ammonium salts used herein are not negated when employed in combination with soaps or the anionic curd dispersants. Apparently, the insoluble nature of the di-long chain quats renders them somewhat campatible with such anionic materials. Whatever the reason, the quaternary ammonium anti-stats herein perform their anti-static function when used in combination with clays and anionics such as soap and curd dispersants. I
The quaternary ammonium anti-static agents used in this invention can be prepared in various ways wellknown in the art. Many such materials are commercially available. The quaternaries are often made from alkyl halide mixturescorresponding to the mixed alkyl chain lengths in fatty acids. For example, the ditallow quaternaries are made from alkyl halides having mixed C C chain lengths. Such mixed di-long chain quaternaries are useful herein and are preferred from a cost standpoint.
As noted above, essentially any anionic group can be the counterion in the quaternary compounds used herein. The anionic groups in the quaternary compounds can be exchanged, one for another, using standard anion exchange resins. Thus, quaternary ammonium salts having any desired anion are readily available. While the nature of such anions has no effect on the compositions and processes of this invention, chloride ion is the preferred counter-ion from a cost standpoint.
The following are representative examples of substantially water-insoluble quaternary ammonium antistatic agents suitable for use in the compositions and processes of the instant invention. All of the quaternary ammonium compounds listed can be formulated in releasable combination with the detergent compositions herein, but the compilation of suitable quaternary compounds hereinafter is only by way of example and is not intended to be limiting of such compounds. Ditallowdimethylammonium chloride is an especially preferred quaternary anti-static agent for use herein by virtue of its low cost, low solubility and high-anti-static activity; other useful di-long chain quaternary compounds are dicetyldimethylammonium chloride; bis-docosyldimethylammonium chloride; didecyldimethylammonium chloride; ditallowdimethylammonium bromide; dioleoyldimethylammonium hydroxide; ditallowdiethylammonium chloride; ditallowdipropylammonium bromide; ditallowdibutylammonium fluoride, cetyldecylmethylethylammonium chloride, bis- [ditallowdim ethylammonium ]sulfate; tris- [ditallowdimethylammonium]-phosphate; and the like.
The Granular Particles The granular particle component of the instant laundering compositions comprises two essential ingredients (l) a water-soluble soap compound and (2) a curd-dispersing agent. In addition, as will be set forth more fully hereinafter, the quaternary ammonium antistatic agent can comprise a third component of the granules, but is more preferably applied to the surfaces of said granules by spraying after the base granules are formed.
Soap Compound The granular particles of the instant invention comprise from about 30% to about 80%, preferably from about 40% to about 70%, by weight of the particles of a soap compound. Useful soap compounds include the ordinary alkali metal soaps such as the sodium, potassium, ammonium and alkanolammonium salts of higher fatty acids containing from about 8 to about 24 carbon atoms, preferably from about 10 to about 20 carbon atoms. Suitable fatty acids can be obtained from natural sources such as, for instance, plant or animal esters (e.g., palm oil, coconut oil, babassu oil, soybean oil, castor oil, tallow, whale and fish oils, grease, lard, and mixtures thereof). The fatty acids also can be synthetically produced (e.g., by the oxidation of petroleum, or by hydrogenation of carbon monoxide by the Fischer- Tropsch process). Resin acids are suitable such as rosin and those resin acids in tall oil. Naphthenic acids are also suitable. Sodium and potassium soaps can be made by direct saponification of the fats and oils or by the neutralization of the free fatty acids which are prepared in a separate manufacturing process. Particularly useful are the sodium and potassium salts of the mixture of fatty acids derived from. coconut oil and tallow, i.e., sodium tallow soap, sodium coconut soap, potassium tallow soap, potassium coconut soap and mixtures thereof.
The Curd Dispersing Agent As noted above, it is well known that the use of soap in hard water results in the formation and precipitation of insoluble fatty acid salts, more commonly referred to as lime soaps, which have a tendency to coagulate and form a sticky curd. To prevent formation of such curd in laundering solutions containing the compositions of the instant invention, the granular particles in addition to the soap component contain from about 1% to about 30%, preferably from about 2% to about 20%, by weight of the particle of a curd-dispersing agent.
, Such curd dispersing agents either prevent the formation of large particles of insoluble lime soaps or prevent such soaps from flocculating so that they are flushed away with the washing or rinsing liquid and do not adhere to fabrics or to surfaces of washing vessels.
The effectiveness of particular materials as curddispersing agents can be ascertained by a simple procedure testing the ability of the test material to peptize lime soaps. Such a procedure is outlined in Schwartz and Perry, Surface Active A gents, lnterscience Publishers, Inc., 1949 at pp. 326 and 327, and is summarized as follows:
The general method consists of preparing a series of mixtures containing varying proportions of sodium oleate and the curd dispersing agent being tested. These mixtures contain approximately 10% total soap-pluscurd dispersant in distilled water. Five milliliters of each mixture are then added to 45 milliliters of hard water (usually 200 ppm hardness as CaO). This is called the first dilution, and it usually results in a turbid but well-dispersed sol. Five milliliters of the first dilution are then added to 45 milliliters of hard water, forming the second dilution. This is a severe test since there is now more than enough lime present to precipitate all the soap. Furthermore, the total soapplus-curd dispersant concentration is of the order of 0.1%. The results are expressed as the percentage of dispersant in the soap-curd dispersant mixture which is just sufficient to prevent flocculation on the second dilution. The more effective the curd dispersing agent, the lower is the percentage value. For purposes of the instant invention a curd dispersing agent is any material which produces a percentage value in the above-described lime soap peptizing procedure of about 39% or less. A conventional non-curd dispersant surfactant for purposes of this invention is a surfactant providing a percentage value greater than 39% in the above-described lime soap peptizing procedure.
Examples of suitable curd-dispersing agents include certain anionic, semipolar nonionic, ampholytic and zwitterionic materials as well as certain amides and amines. Classes of these curd-dispersing agents are more fully described as follows:
(1) Anionic organic detergents which are alkali metal, ammonium and substituted-ammonium salts of esters of a-sulfonated fatty acids in which the esters contain about 12 to about 25 carbon atoms.
These detergent compounds have the following structure:
wherein R is an alkyl and alkenyl moiety of about to about carbon atoms (forming with the two carbon atoms a fatty acid group); R is alkyl of l to about 10 carbon atoms; and M is a salt-forming moiety.
The salt-forming moety M in the hereinbefore described structural formula is a water-solubilizing cation and can be, for example, an alkali metal cation (e.g., sodium, potassium, lithium), ammonium or substituted ammonium cation. Specific examples of substituted ammonium cations include methyl-, dimethyl-, trimethyl-ammonium and triethanolammonium cations and quaternary ammonium cations such as tetramethyl ammonium and dimethyl piperidinium cations and those derived from alkylamines such as ethylamine, diethylamine, triethylamine, mixtures thereof and the like.
Specific examples of this class of compounds include the sodium and potassium salts of esters where R is selected from methyl, ethyl, propyl, butyl, hexyl and octyl groups and the fatty acid group (R, plus the two carbon atoms in the structure above) is selected from lauric, myristic palmitic, stearic, palmitoleic, oleic, linoleic acids and mixtures thereof. A preferred ester material herein is the sodium salt of the methyl ester of a-sulfonated tallow fatty acid, the term tallow indicating a carbon chain distribution approximately as follows: C 2.5%, C 28%, C 23%, palmitoleic 2%, oleic 41.5%, and linoleic-3% (the first three fatty acids listed are saturated).
Other examples of suitable salts of oz-sulfonated fatty esters utilizable herein include the ammonium and tetramethylammonium salts of the hexyl, octyl, ethyl, and butyl esters of a-sulfonated tridecanoic acid; the potassium and sodium salts of the ethyl, butyl, hexyl, octyl, and decyl esters of a-sulfonated pentadecanoic acid, and the sodium and potassium salts of the butyl, hexyl, octyl, and decyl esters of oz-sulfonated heptadecanoic acid; and the lithium and ammonium salts of the butyl, hexyl, octyl, and decyl esters of a-sulfonated nonadecanoic acid.
The salts of a-sulfonated fatty acid esters of the present invention are known compounds and are described in U.S. Pat. No. 3,223,645, issued Dec. 14, 1965 to Kalberg, this patent being hereby incorporated by reference.
2. Anionic organic detergents which are salts of 2-acyloxy-alkanel -sulfonic acids.
These salts have the formula:
R-CH- M CH SO the sodium salt of 2-acetoxy-tridecane-l-sulfonic acid; the potassium salt of 2-propionyloxy-tetradecane-1- sulfonic acid; the lithium salt of Z-butanoyloxytetradecane-l-sulfonic acid; the sodium salt of 2- pentanoyloxy-pentadecane-l-sulfonic acid; the ammonium salt of 2-hexanoyloxy-hexadecane l-sulfonic acid; the sodium salt of 2-acetoxy-hexadecane-l-sulfonic acid; the dimethylammonium salt of 2-heptanoyloxytridecane-l-sulfonic acid; the potassium salt of 2- octanoyloxy-tetradecane-l-sulfonic acid; the dimethylpiperidinium salt of 2-nonanoyloxytetradecane-lsulfonic acid; the sodium salt of 2-acetoxyheptadecane-l-sulfonic acid; the lithium salt of 2- acetoxy-octadecane-l-sulfonic acid; the dimethylamine salt of 2-acetoxy-octadecane-l-sulfonic acid; the potassium salt of 2-acetoxy-nonadecane-l-sulfonic acid; the sodium salt of 2-acetoxy-eicosane-l--sulfonic acid; the sodium salt of 2-propionyloxy-clocosane-lsulfonic acid; and isomers thereof.
Preferred B-acyloxy-alkane-l-sulfonate salts herein are the alkali metal salts of fi-acetoxy-alkane-l-sulfonic acids corresponding to the above formula wherein R is an alkyl moiety of about 12 to about 16 carbon atoms, these salts being preferred from the standpoint of their excellent curd-dispersing properties and ready availability.
Typical examples of the above described B-acetoxy alkanesulfonates are described in the literature: Belgian Pat. No. 650,323 issued July 9, 1963, discloses the preparation of certain 2-acyloxy alkanesulfonic acids. Similarly, U.S. Pats. No. 2,094,451 issued Sept. 28, 1937, To Guenther, et al., and No. 2,086,215 issued July 6, 1937 to De Groote disclose certain salts of ,B-acetoxy alkanesulfonic acids. These patents are hereby incorporated by reference.
3. Anionic organic detergents which are alkyl ether sulfates.
These materials have the formula RO(C H.,0),SO M wherein R is an alkyl or alkenyl moeity of about 10 to about 20 carbon atoms, x is l to 30, and M is a saltforming cation as defined hereinbefore.
The alkyl ether sulfates useful in the present invention as curd dispersants are condensation products of ethylene oxide and monohydric alcohols having about 10 to about 20 carbon atoms. preferably, R has l4 to 18 carbon atoms. The alcohols can be derived from fats, e.g., coconut oil or tallow, or can by synthetic. Lauryl alcohol and straight chain alcohols derived from tallow are preferred herein. Such alcohols are reacted with l to 30, and especially 3 or 6, molar proportions of ethylene oxide and the resulting mixture of molecular species, having, for example, an average of 3 or 6 moles of ethylene oxide per mole of alcohol, is sulfated and neutralized.
Specific examples of alkyl ether sulfates of the present invention are sodium coconut alkyl ethylene glycol ether sulfate; lithium tallow alkyl trialkylene glycol ether sulfate; sodium tallow alkyl hexaoxyethylene sulfate; and ammonium tetradecyl octaoxyethylene sulfate.
Preferred herein for reasons of excellent curddispersing properties and ready availability are the alkali metal coconutand tallow-alkyl oxyethylene ether sulfates having an average of about 3 to about 10 oxyethylene moieties. The alkyl ether sulfates of the present invention are known compounds and are described in U.S. Pat. No. 3,322,876 to Walker (July 25, 1967) incorporated herein by reference.
4. Anionic organic detergents which are olefin sulfonates having about 12 to about 24 carbon atoms.
The term olefin sulfonates is used herein to mean compounds which can be produced by the sulfonation of a-olefins by means of uncomplexed sulfur trioxide, followed by neutralization of the acid reaction mixture using conditions such that any sultones which have been formed in the reaction are hydrolyzed to give the corresponding hydroxy-alkanesulfonates. The sulfur trioxide may be liquid or gaseous, and is usually, but not necessarily, diluted by inert diluents, for example by liquid S chlorinated hydrocarbon, etc., when used in the liquid form, or by air, nitrogen, gaseous S0 etc., when used in the gaseous form.
The a-olefins from which the olefin sulfates are derived are mono-olefins having 12 to 24 carbon atoms, preferably 14 to 16 carbon atoms. Preferably, they are straight chain olefins. Examples of suitable l-olefins include l-dodecene; l-tetradecene; l-hexadecene; loctadecene; l-eicosene and l-tetracosene.
In addition to the true alkene sulfonates and a proportion of hydroxy-alkanesulfonates, the olefin sulfonates can contain minor amounts of other materials, such as alkene disulfonates depending upon the reaction conditions, proportions of reactants, the nature of the starting olefins and impurities in the olefin stock and side reactions during the sulfonation process.
A preferred embodiment herein are those olefin sulfonates which are described completely in US. Pat. No. 3,332,880 issued July 25, 1967, to Kessler, et. al., hereby incorporated by reference.
5. Nonionic organic detergents which are semiplar detergent compounds.
These include, for example, long chain tertiary phosphine oxides having the structure:
. 3 wherein R is alkyl, alkenyl, or monohydroxyalkyl of about 8 to about 18 carbon atoms having from O to about ethylene oxide moieties and from O to l glyceryl moiety and R and R are each alkyl or monohydroxyalkyl groups containing from 1 to about 3 carbon atoms. The arrow in the formula is a conventional representation of the semi-polar bond.
Examples of suitable phosphine oxides are: dodecyldimethylphosphine oxide, tetradecyldimethylphosphine oxide, tetradecylmethylethylphosphine oxide, 3,6,9-trioxaoctadecyldimethylphosphine oxide, cetyldimethylphosphine oxide, 3-dodecoxy-2 hydroxypropyldi( 2-hydroxyethyl phosphine oxide, stearyldimethylphosphine oxide, cetylethylpropylphosphine oxide, oleyldiethylphosphine oxide, dodecyldiethylphosphine oxide, tetradecyldiethylphosphine oxide, dodecyldipropylphosphine oxide, dodecyldi( hydroxymethyl)phosphine oxide, dodecyldi( 2-hydroxyethyl)phosphine oxide, tetradecylmethyl-2-hydroxypropyl phosphine oxide, oleyldimethylphosphine oxide, and
6. Nonionic organic detergents which are certain organic sulfoxides.
Such compounds have the general formula:
X- S CH CH R H l O OH group, e.g., carboxy, sulfonate, sulfate, phosphate, or phosphonate.
These detergents have the formula 2 1 R NCH -R3ZM wherein R is alkyl of about 8 to 18 carbon atoms, R is alkyl of l to about 3 carbon atoms or is hydrogen, R is alkylene of 1 to about 4 carbon atoms, Z is carboxy, sulfonate, sulfate, phosphate or phosphonate and M is a salt-forming cation, as hereinbefore described. Examples of compounds falling within this definition are sodium 3-dodecylaminopropionate; sodium 3- dodecylaminopropane sulfonate; N-alkyltaurines such as the one prepared by reacting dodecylamine with sodium isethionate according to the teaching of US. Pat. No. 2,658,072; sodium salts of N-higher alkyl aspartic acids such as those produced according to the teaching of US. Pat. No. 2,43 8,091; and the products sold under the trade name Miranol and described in US. Pat. No. 2,528,378.
8. Zwitterionic synthetic detergents which are derivatives of aliphatic quaternary ammonium, phosphonium and sulfonium compounds, in which the aliphatic groups can be straight chain or branched, and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains an anionic water solubilizing group, e.g., carboxy, sulfonate, sulfate, phosphate, or phosphonate. A general formula for these compounds is:
l Y CH2 R3 wherein R is an alkyl, alkenyl, hydroxyalkyl or alkylbenzyl group containing from about 8 to about 24 carbon atoms and having from 0 to about 10 etliylene oxide moieties and from 0 to l glyceryl moiety; Y is selected from the group consisting of nitrogen, phosphorus, and sulfur atoms; R is an alkyl or monohydroxy alkyl group containing 1 to about 3 carbon atoms; x is 1 when Y is a sulfur atom and 2 when Y is nitrogen or phosphorus atom, R is an alkylene or hydroxy alkylene group of 1 to about 4 carbon atoms and Z is a member selected from the group consisting of carboxylate, sulfonate, sulfate, phosphonate, and phosphate groups.
4- [N,N-di( Z-hydroxyethyl )'-N-octadecyl-ammonio butane- 1 -carboxylate;
-[S-3-hydroxypropyl-S-hexadecylsulfonio]-3- hydroxypentane- 1 -sulfate; 3-[P,P-diethyl-P- 5 3,6,9trioxatetracosanephosphonio]-2-hydroxypropane- 1 -phosphate; 3-[N,N-dipropyl-N-3-dodecoxy-2-hydroxypropylammonio l-propane -1-phosphonate; 3-( N,N-dimethyl-N-hexadecylammonio )propanel sulfonate; 3-(N.N-dimethyl-N-hexadecyl-ammonio)2- hydroxypropanel -sulfonate; 4-[N,N-di(2-hydroxyethyl)-N- (2hydroxydodecyl )ammonio -butanel carboxylate; v 3-[S-ethyl-S-( 3-dodecoxy-2- hydroxypropyl)sulfonio]-propane- 1 -phosphate; 3-[ P,P-dimethyl-P-dodecylphosphonio]-propanel phosphonate; S- N,N-di( 3-hydroxypropyl )-N-hexadecylammonio -2'hydroxypentane- 1 sulfate; 3-(dodecylbenzyldimethylammonio)propane-1- sulfonate; and 2-(dodecylbenzyldimethylammonio)ethane-1- sulphate. Examples of compounds falling within this definition also includes 3-( N,N-dimethyl-N-hexadecylammonio )propane-l-sulfonate and 3-(N,N-dimethyl- N-hexadecyl-ammonio )-2-hydroxypropane- 1 -sulfonate which are especially preferred herein for their availability and curd dispersant characteristics. Some of the compounds of this type as well as their use as dispersing agents are more fully described in US. Pat. Nos. 2,699,991 and 3,660,470 herein incorporated by reference.
9. Organiccarboxylic acid amides. Such amide compounds include those aliphatic amides of the general formula:
R- CO N R n I 4 5 wherein R is hydrogen, alkyl, or alkylol and R and R" are hydrogen, alkyl, alkylol, or alkylene joined through an oxygen atom, the total number of carbon atoms in R, Rand R" being from about 9 to about 25.
Amides of this general type which are of special utility are those aliphatic carboxylic acid alkanolamides of the formula: V
C(RIRIIRIVII) RCO'N in which RC0 is the acyl group of a soap forming carboxylic acid having from aboutv 10 to about 18 carbon atoms, R and R" are each selected from the group consisting of hydrogen, alkyl, and alkylol substituents, and R' is an alkylol substituent, the total number of carbon atoms in R, R5 and R being from 1 to 7.
Some specific amides coming within the scope of the invention are:
stearic ethanolamide; dimethyl lauramide;
' lauramide; i
lauryl lauramide; myristic N-methyl ethanolamide; butyl capramide; capric butanolamide; dibutyl capramide; dibutyl myristamide; stearic acid amide of tris(hydroxymethyl)amino methane; myristic glycerylamide; N-lauroyl morpholin'e; lauric glycerylamide; palmitic acid vamide of 2-amino-2-methyl-l,3-
propanediol; lauryl hydroxy-acetamide; myristyl formamide; lauric isopropanol amide; and 1 myristic acid amide of 3-amino-3-methyl-2,4-
pentanediol. Especially preferred is tallow acyl monoethanolamide.
Such amides, their preparation and use as dispersing agents are discussed more fully in US. Pat. No. 2,527,076, hereby incorporated by reference.
10. Organic "alkyl and alkanol amines.
Such amine compounds include N-alkyl monoalkylolamines and N-alkyl dialkylolamines in which the alkyl group has from 1010 16 carbon atoms and the alkanol group has 2 or 3 carbon atoms; N-alkyl morpholines in which the alkyl group has from 10 to carbon atoms; and N-alkyl tris( hydroxymethyl)aminomethane in which the alkyl group has from 10 to 16 carbon atoms. l
Specific examples of such compounds include N-dodecylmonoethanolamine, N-dodecyl-tris(hydroxymethyl )aminomethane N-dodecyl isopropanolamine, N-tetradecyl monoethanolamine, N-dodecyl diethanolamine, N-tetradecyl diethanolamine and N-dodecyl morpholine. Compounds of this type and their use as curd-dispersing agents are described more fully in British Pat. No. 1,006,836, incorporated herein by reference.
Of all the above-described types of curd-dispersing agents, the compounds preferred for use in the granular particles of the instant composition include the sodium salt of the methyl ester of a-sulfonated tallow the alkyl group averages about 14.8 carbon atoms in length; hexadecylammonio )propane-v l -sulfonate; dimethyl-N-hexadecylammonio)Q-hydroxypropane l sulfonate; 3-( N -dodecylbenzene -N,N-dimethyl ammonio )-propane-l-sulfonate and tallow acyl monoethanolamide. Y i i Highly preferred curd dispersing agents herein are the sodium salt of ethoxylated tallow alkyl sulfate averaging about 3 ethylene oxide groups per mole, the sodium salt of ethoxylated tallow alkyl sulfate average about 6 ethylene oxide groups per mole, and tallow acyl monoethanolamide.
Optional Granule Components Besides the above-described soap and curddispersing components, the granular particles of the instant compositions can contain a wide variety of optional components generally found in conventional fabric laundering formulations. Such optional components include, for example, conventional anionic or nonionic surfactants which are not particularly useful as curd dispersants and alkaline builder salts. Such non-curddispersing surfactants are those having a percentage value in the above-described lime soap peptizing test greater than 39% and include the sodium salts of linear alkyl benzene sulfonac acid where the alkyl group average about 10 to 18 carbon atoms in length, sodium tallow alkyl sulfate, the condensation product of coconut 'fatty alcohol with about 6 moles of ethylene oxide per mole of alcohol, and the condensation product of a secondary fatty alcohol containing about carbon atoms with about 9 moles of ethylene oxide per mole of alcohol. When employed, such conventional non-curddispersing surfactants generally comprise from about 1% to 30% by weight of the granular particle.
Typical alkaline builders include sodium tripolyphosphate, sodium citrate, sodium nitrilotriacetate, sodium carbonate and sodium mellitate. When employed, such conventional builders generally comprise from about 1% to 30% by weight of the granular particle.
Other optional granule components include the various soil-suspending agents such as carboxymethylcellulose, corrosion inhibitors, dyes, fillers such as sodium sulfate and silica, optical brighteners, bleaches such as sodium perborate, suds boosters, suds depressants, germicides, antitarnishing agents, pH adjusting agents such as sodium silicate, enzymes, and the like, well known in the art for use in detergent compositions. Bound water can also be present in said compositions.
The soap-based granules herein can be prepared in standard fashion, e.g., by blending the soap, curd dispersant and optional ingredients of the granules in a crutcher, and subsequently blowing the mix in standard spray-drying equipment.
Clay Compounds The present compositions contain, as an essential ingredient, particulate smectite-type clay materials which increase the solubility of the combined soap-curd dispersant granules and provide fabric softening concurrently with fabric cleansing. These smectite clays are present in the detergent compositions at concentrations from about 4% to about 25%, preferably from 5% to 15% by weight, of the total composition. The weight ratio of clay to the soap-based granules is from about 20:1 to about 3:1 by weight.
The clay minerals used to provide the solubility and softening properties of the instant compositions can be described as impalpable, expandable, three-layer clays, i.e., alumino-silicates and magnesium silicates, having an ion exchange capacity of at least about 50 meg/100 g. of clay. The term impalpable as used to describe the clays employed herein means that the individual clay particles are of a size that they cannot be perceived tactilely. Such particle sizes are within the range below about 50 microns. In general, the clays herein will have a particle size within the range of from about 5 microns to about 25 microns. The term expandable as used to describe clays relates to the ability of the layered clay structure to be swollen, or expanded, on contact with water. The three-layer expandable clays used herein are those materials classified geologically as smectites.
There are two distinct classes of smectite-type clays. In the first, aluminum oxide is present in the silicate crystal lattice; in the second class of smectites, magnesium oxide is present in the silicate crystal lattice. The general formulas of these smectites are Al SE0 (Ol-l) and Mg (Si O (OI-D for the aluminum and magnesium oxide type clay, respectively. It is to be rec ognized that the range of the water of hydration in the above formulas can vary with the processing to which the clay has been subjected. This is immaterial to the use of smectite clays in the present invention in that the expandable characteristics of the hydrated clays are dictated by the silicate lattice structure. Furthermore, atom substitution by iron and magnesium can occur within the crystal lattice of the smectites, while metal cations such as Na+, Ca+l-, as well as 1-1+, can be copresent in the water of hydration to provide electrical neutrality. Except as noted hereinafter, such cation substitutions are immaterial to the use of the clays herein since the desirable physical properties of the clays are not substantially altered thereby.
The three-layer, expandable alumino'silicates useful herein are further characterized by a dioctahedral crystal lattice, while the expandable three-layer magnesium silicates have a trioctahedral crystal lattice.
As noted hereinabove, the clays employed in the compositions of the instant invention contain cationic counterions such as protons, sodium ions, potassium ions, calcium ion, magnesium ion, and the like. It is customary to distinguish between clays on the basis of one cation predominantly or exclusively absorbed. For example, a sodium clay is one in which the absorbed cation is predominantly sodium. Such absorbed cations can become involved in exchange reactions with cations present in aqueous solutions. A typical exchange reaction involving a smectite-type clay is expressed by the following equation:
smectite clay (Na) NH OH (Ni-l NaOl-l Since in the foregoing equilibrium reaction, one equivalent weight of ammonium ion replaces an equivalent weight of sodium, it is customary to measure clay cation exchange capacity (sometimes termed base exchange capacity) in terms of milliequivalents per g. of clay (meq/lOO g.). The cation exchange capacity of clays can be measured in several ways, including by electrodialysis, by exchange with ammonium ion followed by titration, or by a methylene blue procedure, all as fully set forth in Grimshaw, The Chemist y and Physics of Clays, lnterscience Publishers, Inc. pp. 264-265 (1971). The cation exchange capacity of a clay mineral relates to such factors as the expandable properties of the clay, the charge of the clay, which, in turn, is determined at least in part by the lattice structure, and the like. The ion exchange capacity of clays varies widely in the range from about 2 meq/ 100 g. for kaolinites to about meq/lOO g., and greater, for
(- smectite clay certain clay of the montmorillonite variety. Illite clays have an ion exchange capacity somehwere in the lower portion of the range, i.e., around 26 meq/ 100 g. for an average illite clay.
It has been determined that illite and kaolinite clays, with their relatively low ion exchange capacities, are not useful in the instant compositions. Indeed, such illite and kaolinite clays constitute a major component of clay soils and, are, in fact, removed from fabric surfaces by means of the instant compositions. However, smectites, such as nontronite, having an ion exchange capacity of approximately 50 meq/ 100 g., saponite, which has an ion exchange capacity of around 70 meq/ l 00 g., and montmorillonite, which has an ion exchange capacity greater than 70 meq/lOO g., have been found to be useful in the instant compositions. This is so since such smectites, if attached to the granule surface, increase composition solubility while, once added to laundering liquor, deposit on the fabrics to provide softening. Accordingly, clay minerals useful herein can be characerized as impalpable, expandable, three-layer smectite-type clays having an ion exchange capacity of at least about 50 meq/ 100 g.
The smectite clays used in the compositions herein are all commercially available. Such clays include, for example, montmorillonite, volchonskoite, nontronite, hectorite, spaonite, sauconite, and vermiculite. The clays herein are available under commercial names such as fooler clay (clay found in a relatively thin vein above the main bentonite or montmorillonite veins in the Black Hills) and various tradenames such as Thixogel No. 1 (also, Thixo-Jell) and Gelwhite GP from Georgia Kaolin Co., Elizabeth, N.J.; Volclay BC and Volclay No. 325, from American Colloid Co., Skokie, Ill.; Black Hills Bentonite Bl-I 450, from international Minerals and Chemicals; and Veegum Pro and Veegum F, From R. T. Vanderbilt. It is to be recognized that such smectite-type minerals obtained under the foregoing commercial and tradenames can comprise mixtures of the various discreet mineral entities. Such mixtures of the smectite minerals are suitable for use herein.
While any of the impalpable smectite-type clays having a cation exchange capacity of at least about 50 meq/ 100 g. are useful herein, certain clays are preferred. For example, Gelwhite GP and fooler clay are extremely white forms of smectite clays and are therefore preferred when formulating white, granular compositions. Volclay BC, which is a smectite-type clay mineral containing at least 3% iron (expressed as Fe O in the crystal lattice, and which has a very high ion exchange capacity, is one of the most efficient andeffective clays for use in laundry compositions and is preferred from the standpoint of fabric softening performance. Likewise, Thixogel No. l, is a preferred clay herein from the standpoint of both product solubility and through-the-wash fabric softening performance. On the other hand, certain smectite clays, such as those marketed under the name bentonite, are sufficiently contaminated by other silicate minerals that their ion exchange capacity falls below the requisite range, and such clays are of no use in the instant compositions.
Appropriate clay minerals for use herein can be selected by virtue of the fact that smectites exhibit a true 14A x-ray diffraction pattern. This characteristic pattern, together with exchange capacity measurements performed in the manner noted above, provides a basis for selecting suitable impalpable smectite'type clay minerals for use in the granular detergent compositions disclosed herein.
COMPOSITION PREPARATION The compositions herein can be formulated by simply preparing granules comprising the soap, curd dispersant, and any of the optional ingredients mentioned hereinabove. The granules are then sprayed with a quaternary ammonium compound from a melt and then contacted with the smectite-type clay. When this procedure is used, the clay can then be simply admixed, e.g., by tumbling, with the soap-based granules and blended. When this method is employed, the clay is attached to the soapbased granules mainly by surface forces between the clay and soap granules.
In a preferred method for attaching the clay to the granules, the soap-based granules are coated with a material of the type hereinafter disclosed which promotes adhesion of the clay particles to the surface of the granules. When an adhesion-promoting material is used, the substantially dry soap-based granules can be first sprayed with said material in liquid form and then admixed with the clay. The clay and sprayed granules are then thoroughly blended to provide good contact and optimum coating of the granules with the clay. In an alternate procedure, the clay and granules are concurrently admixed and sprayed with the adhesionpromoting material. Mixing of the clay and granules can be achieved using a standard drum mixer. Following this, the quaternary ammonium anti-static agent can be added to the compositions, e.g., by spraying from a melt.
Whatever the method chosen for admixing the soapbased granules, clay and anti-static agent, it is necessary to insure that the quaternary anti-static agent is not affixed to the surface of the clay by chemical bonding. That is to say, if the clay and quat combine by an ion exchange mechanism, the quat is not released to perform its desirable anti-static function when the compositions are admixed with water. The preferred way to avoid ion exchange reactions between the quat and clay is to add the quat to the compositions from a melt, rather than from a solution or suspension in water.
The materials which can be optionally used herein to promote the adhesion of the clays to the surface of the granules can be any water-soluble or water-disperable organic materials, preferably those which are liquids or are liquifiable at convenient temperatures for spraying, i.e., at temperatures from about 60F to about F. Of course, the adhesion-promoting materials used herein should not be toxic or deleterious to fabrics. Since most soap compositions are desirably white in color, colorless organic materials are preferred herein for attaching the clay to the soap-based granules. Preferably, the materials used herein have sufficient hydrophilic character that they are easily dissolved or dispersed in water, but they are preferably not hygroscopic.
A variety of liquid and liquifiable organic compounds are useful herein for attaching the clay to the surface of the soap-based granules. For example, a all manner of common ethoxylated nonionic surfactants can be used for this purpose. Nonionic surfactants produced by the condensation of an alkylene oxide moiety (hydrophilic in nature) with an organic hydrophobic compound which is usually aliphatic or alkyl aromatic in nature can be used. The length of the hydrophilic or polyoxyalkylene moiety which is condensed with any particular hydrophobic compound can be readily adjusted to yield colorless, liquid or liquifiable, water dispensable, organic, nonionic surfactants which are useful adhesion promoters herein. Examples of nonionic surfactants which can be used as the adhesionpromoting materials herein include:
1. The polyethylene oxide condensates of alkyl phenols. These compounds include the condensation prod ucts of alkyl phenols having an alkyl group containing from about 6 to 12 carbon atoms, in either a straight chain or branched chain configuration, with ethylene oxide, said ethylene oxide being present in amounts equal to to 25 moles of ethylene oxide per mole of alkyl phenol. The alkyl substituent in such compounds can be derived, for example, from polymerized propylene, diisobutylene, octene, or nonene. Examples of compounds of this type include nonyl phenol condensed with about 9.5 moles of ethylene oxide per mole of nonyl phenol, dodecyl phenol condensed with about 12 moles of ethylene oxide per mole of phenol, dinonyl 'phenol condensed with about 15 moles of ethylene oxide per mole of phenol, di-isooctylphenol condensed with about 15 moles of ethylene oxide per mole of phenol. Commercially available nonionic surfactants of this type include lgepal CO-6l0 marketed by the GAF Corporation; and Triton X-45, X-l l4, X-l00 and X- 102, all marketed by the Rohm and Haas Company.
2. The condensation product of aliphatic alcohols with ethylene oxide. The alkyl chain of the aliphatic alcohol can either be straight or branched and generally contains from about 8 to about 22 carbon atoms. Examples of such ethoxylated alcohols include the condensation product of about 6 moles of ethylene oxide with 1 mole of tridecanol, myristyl alcohol condensed with about 10 moles of ethylene oxide per mole of myristyl alcohol, the condensation product of ethylene oxide with coconut fatty alcohol wherein the coconut alcohol is a mixture of fatty alcohols with alkyl chains varying from 10 to 14 carbon atoms and wherein the condensate contains about 6 moles of ethylene oxide per mole of alcohol, and the condensation product of about 9 moles of ethylene oxide with the abovedescribed coconut alcohol. Examples of commercially available nonionic surfactants of this type include Tergitol 15-S-9 marketed by the Union Carbide Corporation, Neodol 23-65 marketed by the Shell Chemical Company, and Kyro EOB marketed by The Procter and Gamble Company.
3. The condensation products of ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol. The hydropho' bic portion of these compounds has a molecular weight of from about 1,500 to 1,800. The addition of polyoxyethylene moieties to this hydrophobic portion tends to increase the water-solubility of the molecule as a whole, and the liquid character of the product is re tained up to the point where the polyoxyethylene content is about 50% of the total weight of the condensation product. Examples of compounds of this type in clude certain of the commercially available Pluronic surfactants marketed by the Wyandotte Chemicals Corporation.
4. The condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine. The hydrophobic base of these products consists of the reaction product of ethylenediamine and excess propylene oxide, said base having a molecular weight of from about 2,500 to about 3,000. This base is condensed with ethylene oxide to the extent that the condensation product contains from about 40% to about by weight of polyoxyethylene and has a molecular weight of from about 5,000 to about 1 1,000. Examples of this type of nonionic surfactant include certain of the commercially available Tetronic compounds marketed by the Wyandotte Chemicals Corporation.
The fatty acids are another class of materials which can be used to promote the attachment of the clays to the surface of the granules. Fatty acids useful herein are those C, to C straight chain and branched chain aliphatic carboxylic acids which can be obtained, for example, by the saponification of triglycerides. Both saturated and unsaturated fatty acids are useful herein. Mixtures of fatty acids obtainable from certain designated fats, e.g., tallow fatty acids, obtainable from tallow; coconut fatty acids, obtainable from coconut oil, and; palm fatty acids, obtainable from palm oil, are also useful herein. The C to C aliphatic fatty acids, and mixtures thereof, are preferred members of this class of adhesion-promoting materials herein.
Exemplary fatty acids which can be employed herein to affix the clay to the soap-based granules include lauric, myristic, palmitic, stearic, elaidic, oleic and eicosanoic acids, and mixtures thereof.
The fatty alcohols having C to C hydrocarbon chains are also useful herein as adhesion promoters. These materials can be obtained in a variety of ways well known in the art, e.g., from various triglyceride oils such as palm oil and coconut oil. Exemplary alcohols useful herein include l-dodecanol, l-tetradecanol, l-hexadecanol and l-octadecanol.
Preferred materials which can be used herein to attach the smectite clays to the surfaces of the soap-pluscurd dispersant granules include: coconut alcohol ethoxylate containing 6 ethylene oxide units per molecule; tallow alcohol ethoxylate containing 11 ethylene oxide units per molecule, i.e., tallow ethylene oxide (1 1); coconut fatty acid mixtures; tallow fatty acid mixtures, the condensate of one mole of ethylene oxide with l-dodecanol; and the condensate of one mole of l-dodecanol with ethylene oxide hexamer. Especially preferred adhesion promoters herein include coconut fatty acids and tallow ethylene oxide (1 1).
In addition to providing good attachment of the smectite-type clays to the surface of the soap-based granules herein, the optionally employed adhesionpromoting materials serve the additional function of providing an unexpected additional increment of solubility to the compositions. That is to say, while the soap-plus-curd dispersant granules herein exhibit poor solubility in laundering baths on the range of from about 60F. to F., the surface coating of the adhesion-promoting materials enhances this solubility. While the soap-plus-curd dispersant granules coated with the adhesion-promoting materials are not rendered sufficiently soluble to be optimally useful for cool water washing (i.e., at about 80F), the added increment of solubility imparted by the adhesionpromoting materials complements the substantial increase in solubility afforded by the smectite-type clays. Accordingly, the soap-based granules coated with the adhesion promoter and having the smectite-type clays attached to the surface have a water solubility comparable to that of the better commercial synthetic detergent compositions over a wide temperature range.
In addition to providing optimal attachment of the smectite clays to the soap-based granules and enhancing the water solubility of the compositions herein, the optionally-employed, adhesion-promoting materials serve to decrease product dust levels. The decreased product dust levels afforded by the adhesion promoters aids in processing and provides a more acceptable product for the consumer.
When the adhesion-promoting materials herein are employed to attach the smectite-type clays to the surface of the soap-based granules, they are preferably used in an amount sufficient to provide said granules with at least a monolayer coating of said materials. For most purposes, the adhesion-promoting material can comprise from about 0.5% to about 8%, preferably 1% to about 4% by weight of the total composition. Of course, higher proportions of the adhesion promoters can be employed, but this represents an economic waste in that such increased proportions are not required to affix the clay to the granules and do not further increase product solubility to any substantial degree.
Use of the clay-to-soap-based granules ratio noted hereinabove results in compositions wherein a substantial proportion of the surface of the granules are coated with the clay. Of course, when the adhesion-promoting materials are additionally employed, greater coverage of the granules is more easily achieved. While soapbased granules having about and greater, of their surfaces coated with the clay exhibit the desirable solubility properties disclosed herein, it is preferred that the clay coat at least about 40% of the granule surface. Such higher degrees of surface coating are most readily achieved by use of the adhesion-promoting materials disclosed above.
For fabric laundering, softening, and anti-static purposes, the compositions of the instant invention are added to an aqueous laundering liquor to the extent of from about 0.02% to about 2% by weight, preferably from about 0.1% to about 1% by weight. Addition of such compositions provide a laundering liquor pH of from about 6 to 11.
The laundering compositions of the instant invention are illustrated by the following examples:
EXAMPLE 1 A soap-based laundry granule is prepared having the following composition:
Component Sodium soap Potassium soap TAE S C ,,LAS Sodium silicate Sodium sulfate Brightener Perfume Water Miscellaneous Balance The foregoing ingredients are mixed in a crutcher and spray-dried to provide a granular, soap-based composition.
Eighty-eight and four-tenths parts by weight of the soap-based granules prepared above are admixed with l 1.6 parts by weight of an impalpable sodium montmorillonite clay having an ion exchange capacity greater than 50 meq/ g. marketed under the tradename Thixogel No. 1. Such admixture provides a composition comprising the soap-plus-curd dispersant granules having the clay attached to the surface of the granules.
The foregoing soap-plus-clay granules are sprayed with melted ditallowdimethylammonium chloride antistat; a total of 5% by weight of the final composition comprises said anti-stat.
The foregoing composition is added to an aqueous laundering liquor at 100F at a concentration of about 0.12% by weight. The composition rapidly dissolves and the clay and anti-stat are uniformly and independently dispersed throughout the laundering liquor. Fabrics laundered in said liquor are concurrently cleansed, softened and provided with an anti-static finish; substantially no curd buildup occurs.
EXAMPLE I] A soap-based laundry granule is prepared having the following composition:
Component Sodium soap Potassium soap TAE S C LAS Sodium silicate Sodium sulfate Brightener Perfume Water Miscellaneous 3. Balance The foregoing ingredients are mixed in a crutcher and spray-dried to provide a granular, soap-based composition.
The foregoing granular product is then sprayed with a melt of ditallowdimethylammonium chloride to a total of 5% by weight of the granules.
Eighty-eight and four-tenths parts by weight of the soap-based granules coated with the ditallowdimethylammonium chloride prepared above are admixed with 8.6 parts by weight of impalpable sodium montmorillonite clay having an ion exchange capacity greater than 50 meq/ 100 g., marketed under the tradename, Thixogel No. l. The admixed clay and soapbased granules are sprayed with liquid coconut fatty acid and mixing is continued to provide uniform soapplus-curd dispersant-plus-quat granules having the clay attached to the surface. Enough coconut fatty acid is employed to provide about 3% by weight of the total composition.
The foregoing composition is a stable laundry detergent formulation having excellent water dispersability and providing excellent fabric laundering, fabric softening, and fabric anti-static characteristics when added to laundering liquors to the extent of about 0.12% by weight.
EXAMPLE III A soap-based laundry granule is prepared having the following composition:
Component Sodium soap Tallow monoethanolamide Sodium tripolyphosphate l Sodium ethylenediaminetetraacetate Sodium silicate Carboxymethylcellulose Sodium perborate Perfume, brightener. moisture & Misc.
Balance A mixture of tallow and coconut soaps comprising 80% tallow soap and coconut soap.
.The quantity of said anti-stat is adjusted to provide a coating comprising 5% by weight of the total granules.
Ninety-five parts by weight of the soap-based granules coated with the anti-stat prepared above are admixed with 5 parts by weight of an impalpable sodium montmorillonite clay having an ion exchange capacity of about 85-100 meq/ 100 g., marketed under the tradename Volclay BC. Such admixture provides a composition comprising the soap-plus-curd dispersant plus anti-stat granules having the clay attached to the surface.
The foregoing composition provides excellent fabric laundering and has desirable solubility, fabric softening and anti-static characteristics when used to launder fabrics in an aqueous liquor at concentrations of about 0.7% by weight.
EXAMPLE IV A soap-based laundry granule is prepared having the following composition:
Component miscellaneous Balance A mixture of tallow and coconut soaps comprising 80% tallow soap and 20% coconut soap.
The foregoing ingredients are mixed in a crutcher and spray-dried to provide a granular, soap-based composition.
Ninety-two parts by weight of the soap-based granules prepared above are admixed with 5 parts by weight of an impalpable sodium montmorillonite clay having an ion exchange capacity of about 85-100 meq/ 100 g., marketed under the tradename Volclay BC, and 3 parts by weight of a liquid coconut fatty acid. Mixing is continued to provide uniform soap-plus-curd dispersant granule having the clay attached to the surface of such granules.
The foregoing composition is then uniformly admixed with impalpable particles of ditallowdimethylammonium chloride anti-stat. The final concentration of anti-stat in the composition is 7% by weight.
The composition is added to an aqueous laundry bath at F at a concentration of 0.5% by weight. Said laundering bath provides excellent fabric laundering and imparts desirable fabric softening and anti-static characteristics to nylon, cotton, polyester-and polyester/- cotton blends laundered therein.
It is to be recognized that various substitutions for the components of the compositions set forth hereinabove can be made without obviating the advantageous properties of said compositions. For example, substantially similar results are obtained when, in the abovedescribed compositions, the ethoxylated tallow alkyl sulfate curd dispersing agent of the Example I and II compositions, or the tallow monoethanolamide curddispersing agent of the Example III and IV compositions, is replaced with equivalent amounts of the sodium salt of the methyl ester of a-sulfonated tallow fatty acid; the sodium salt of ethoxylated tallow alkyl sulfate having an average of about 6 ethylene oxide groups per mole; sodium B-acetoxy-hexadecane-lsulfonate; sodium B-acetoxy tridecane-l-sulfonate; the sodium salt of sulfonated l-hexadecene; dimethyldodecylphosphine oxide; sodium hexadecylmethylaminopropionate; 3(N,N-dimethyl-N- alkylammonio )-propanel -sulfonate and 3(N,N- dimethyl-N-alkylammonio )-2-hydroxypropanel sulfonate wherein in both compounds the alkyl group averages 14.8 carbon atoms in length; 3 (N,N- dimethyl-N-hexadecylammonio)-propanel -sulfonate; 3(N,N-dimethyl-N-hexadecylammonio)-2- hydroxypropanel -sulfonate; 3-( N-dodecylbenzyl- N ,N-dimethylammonio )-propanel -sulfonate; methyl- B-hydroxydodecyl sulfoxide; stearic ethanolamide; or N-dodecylmonoethanolamine, respectively.
Substantially similar results are obtained, when in the above-described compositions, the Thixogel No. l clay of the Example I and II compositions or the Volclay BC of the Example III and IV compositions is replaced with an equivalent amount of fooler clay, Gelwhite GP, Volclay No. 325, Black Hills Bentonite BH 450, Veegum Pro or Veegum F, respectively.
Substantially similar results are obtained when, in the above-described mixes, the sodium linear alkyl benzene sulfonate non-curd-dispersing surfactant of the Example I and II compositions is replaced with an equivalent amount of sodium tallow alkyl sulfate; the condensation product of coconut fatty alcohol with about 6 moles of ethylene oxide per mole of alcohol; or the condensation product of a secondary fatty alcohol containing about 15 carbon atoms with about 9 moles of ethylene oxide per mole of alcohol, respectively.
Substantially similar results are obtained when, in the above-described compositions, the sodium tripolyphosphate builder of the Example III and IV compositions is replaced with an equivalent amount of sodium citrate, sodium carbonate, sodium mellitate or sodium nitrilotriacetate, respectively.
Subsequently similar results are obtained when, in the above-described compositions, the coconut fatty acid adhesion-promoting agent of the Example II and Example IV compositions is replaced with an equivalent amount of coconut alcohol ethoxylate containing 6 ethylene oxide units per mole; tallow alcohol ethoxylate containing 1 l ethylene oxide units per mole; tallow fatty acid mixtures, the condensate of one mole of ethylene oxide with l-dodecanol; the condensate of one mole of l-dodecanol with ethylene oxide hexamer; or the condensate of 9.5 moles of ethylene oxide with nonyl phenol, respectively.
Equivalent anti-static results are obtained in the above-described compositions when the ditallowdimethylammonium chloride is replaced by an equivalent amount of ditallowdirnethylammonium bromide; ditallowdimethylammonium hydroxide; ditallowdiethylammonium chloride; dioctadecyldibutylammonium iodide; oleoyldecylmethylbutylammonium chloride; bisditallowdibutylammonium carbonate and [ditallowdiethylammonium ]phosphate respectively.
As seen from the foregoing, compositions comprising from about 75% to about 96% by weight of a soapbased granule containing a curd dispersant, from about 0.5% to about 15% by weight of a quaternary ammonium anti-static agent and from about 4% to about 25% by weight of a smectite-type clay, provide excellent through-the-wash fabric cleansing, softening and antistatic benefits.
What is claimed is:
l. A fabric laundering composition, comprising:
A. from about 75% to about 96% by weight of granular particles which comprise i. from about 30% to about 80% by weight of said granular particles of a soap compound, and
ii. from about 1% to about 30% by weight of said granular particles of a curd-dispersing agent;
B. from about 4% to about 25% by weight of an impalpable smectite-type clay having an ion exchange capacity of at least about 50 meq/lOO grams, attached to the surface of said granular particles, said composition having a weight ratio of granular particles to impalpable smectite-type clay of from about 20:1 to 3:]; and
C. from about 0.5% to about 15% by weight of a substantially water-insoluble quaternary ammonium anti-static agent of the formula wherein each R is a hydrocarbyl group containing from about 10 to about 22 carbon atoms and each R is a hydrocarbyl group containing from about 1 to about 4 carbon atoms, X is an anion and n is an integer from 1 to 3, the weight ratio of smectitetype clay to quaternary ammonium compound being in the range of from about 40:1 to about 1:1, said quaternary ammonium compound being in releasable combination in said composition.
2. A composition according to claim 1:
A. wherein the soap compound is a water-soluble salt of a higher fatty acid containing from about 8 to about 24 carbon atoms and is present in said granular particles to the extent of from about 40% to about 70% by weight of the granular particles;
B. wherein the curd-dispersing agent is selected from the group consisting of i. compounds of the formula III ll wherein R, is alkyl or alkenyl of about 10 to 20 carbon atoms, R is alkyl of 1 to about 10 carbon atoms and M is a salt-forming cation;
ii. compounds of the formula tris- 7 u OCR R C CH SO M wherein R is alkyl of about 9 to about 23 carbon atoms, R is alkyl of lto about 8 carbon atoms and M is a salt-forming cation; iii. compounds of the formula RO(C H O) 50 M wherein R is alkyl or alkenyl of about 10 to about 20 carbon atoms, x is l to 30 and M is a saltforming cation;
iv. olefin sulfonates containing from about 12 to 24 carbon atoms;
v. compounds of the formula X S CH CH R l! 2 O OH wherein R is an alkyl group of from about 8 to 16 carbon atoms and X is selected from the group consisting of methyl, ethyl and B-hydroxyethyl groups; vii. compounds of the formula R N CH2 R3 ZM wherein R is alkyl of about 8 to 18 carbon atoms, R is selected from the group consisting of alkyl of 1 to about 3 carbon atoms and hydrogen, R is alkylene of 1 to about 4 carbon atoms, Z is selected from the group consisting of carboxy, sulfonate, sulfate, phosphate and phosphonate, and M is a salt-forming cation.
viii. compounds of the formula wherein R is selected from the group consisting of alkyl, alkenyl, hydroxyalkyl and alkylbenzene groups, all groups containing from about 8 to about 24 carbon atoms and having from 0 to about 10 ethylene oxide moieties and from O to l glyceryl moiety; Y is selected from the group consisting of nitrogen, phosphorus, and sulfur atoms; R is an alkyl or monohydroxy alkyl group containing 1 to about 3 carbon atoms; x is 1 when Y is a sulfur atom and 2 when Y is a nitrogen or phosphorus atom, R is alkylene or hydroxyalkylene of from 1 to about 4 carbon atoms and Z is a group selected from the group consisting of carboxylate, sulfonate, sulfate, phosphonate, and phosphate groups; ix. compounds of the formula RI R-CO-N wherein R is hydrogen, alkyl or alkylol and R and R" are each hydrogen, alkyl, alkylol, or alkylene joined through an oxygen atom, the total number of carbon atoms in R, R and R being from about 9 to about 25; and organic amines selected from the group consisting of N-alkyl monoalkylolamines and N-alkyl dialkylolamines wherein the alkyl group contains from about to 16 carbon atoms and the alkylol group contains 2 or 3 carbon atoms; N-alkyl morpholines wherein the alkyl groups contains from about 10 to 16 carbon atoms and N-alkyl tris(hydroxymethyl)-aminomethane wherein the alkyl group contains from about 10 to 16 carbon atoms; and wherein said curddispersing agent is present in said granular particles to the extent of from about 2% to about 20% by weight of said granular particles;
C. wherein said impalpable smectite-type clay is selected from the group consisting of dioctahedral expandable three-layer aluminum-silicates and trioctahedral expandable three-layer magensium silicates, and is present to the extent of from about 4% to about by weight of the total compositon; and
D. wherein the quaternary ammonium compound is ditallowdimethylammonium chloride and is present in releasable combination with the composition at a concentration of from about 0.5% to about 5% by weight.
3. A composition according to claim 1 A. wherein the soap is selected from the group consisting of sodium tallow soap, sodium coconut soap, potassium tallow soap, potassium coconut soap and mixtures thereof;
B. wherein the curd-dispersing agent is selected from the group consisting of the sodium salt of the methyl ester of a-sulfonated tallow fatty acid; the sodium salt of ethoxylated tallow alkyl sulfate having an average of about 3 ethylene oxide groups per mole; the sodium salt of ethoxylated tallow alkyl sulfate having an average of about 6 ethylene oxide groups per mole; sodium B-acetoxy-hexadecane-lsulfonate; sodium-B-acetoxy tridecane- 1 -sulfonate; the sodium salt of sulfonated l-hexadecene; dimethyldodecylphosphine oxide; sodium hexadecylmethylaminopripionate; 3( N,N-dimethyl-N- alkylammonio)-propane-l-sulfonat and 3(N,N-
dimethyl-N-hexade cylammonio )-2- hydroxypropane- 1 -sulfonate; 3-( N-dodecylbenzyl- N,N-dimethylammonio)-propane-1-sulfonate; and tallow acyl monoethanolamide;
C. wherein the smectite-type clay is selected from the group consisting of montmorillonites, volchonskoites, nontronites, hectorites, sauconites and vermiculites; and
D. wherein the quaternary ammonium compound is ditallowdimethylammonium chloride.
4. A composition according to claim 1 wherein the smectite-type clay is selected from the group consisting of fooler clay, Thixogel No. l, Gelwhite GP, Volclay BC, VolclayNo. 325, Black Hills Bentonite Bl-l 450, Veegum Pro and Veegum F.
5. A composition according to claim 1 wherein the smectite-type clay is Volclay BC.
6. A composition according to claim 1 wherein the smectite-type clay is fooler clay.
7. A composition according to claim 1 wherein the curd-dispersing agent is the sodium salt of ethoxylated tallow alkyl sulfate having an average of about 3 ethylene oxide groups per mole and the smectite-type clay is Thixogel No. l.
8. A composition according to claim 1 containing as an additional component from about 0.5% to about 8% by weight of an adhesion-promoting material.
9. A composition according to claim 1 containing as an additional component from about 1% to about 30% by weight of an alkaline builder salt.
10. A composition according to claim 9 wherein the alkaline builder salt is sodium tripolyphosphate.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3716488 *||Aug 11, 1971||Feb 13, 1973||Stevens & Co Inc J P||Textile fabric cleaning compositions|
|US3765911 *||Oct 27, 1970||Oct 16, 1973||London Oil Refining Co||Processing of rubber and the like, and to processing compositions therefor|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4234465 *||Mar 27, 1979||Nov 18, 1980||The Lion Fat & Oil Co., Ltd.||Detergent composition|
|US4308024 *||Oct 31, 1979||Dec 29, 1981||Lever Brothers Company||Fabric softening composition|
|US4339335 *||Mar 27, 1980||Jul 13, 1982||Colgate Palmolive Co.||Free flowing high bulk density particulate detergent-softener|
|US4419250 *||Apr 8, 1982||Dec 6, 1983||Colgate-Palmolive Company||Agglomerated bentonite particles for incorporation in heavy duty particulate laundry softening detergent compositions.|
|US4421657 *||Apr 8, 1982||Dec 20, 1983||Colgate-Palmolive Company||Heavy duty laundry softening detergent composition and method for manufacture thereof|
|US4482471 *||Nov 21, 1983||Nov 13, 1984||Colgate-Palmolive Company||Siliconate-coated sodium perborate|
|US4482477 *||Nov 21, 1983||Nov 13, 1984||Colgate-Palmolive Company||Particulate detergent containing siliconate, composition and method for manufacture thereof|
|US4482630 *||Nov 21, 1983||Nov 13, 1984||Colgate-Palmolive Company||Siliconate-coated enzyme|
|US4488972 *||Apr 8, 1982||Dec 18, 1984||Colgate-Palmolive Company||Bentonite agglomerates|
|US4526702 *||Aug 25, 1982||Jul 2, 1985||Colgate Palmolive Co.||Process for manufacturing bentonite-containing particulate fabric softening detergent composition|
|US4536316 *||Jun 1, 1983||Aug 20, 1985||Colgate-Palmolive Co.||Fabric softening composition containing surface modified clay|
|US4664817 *||Mar 5, 1982||May 12, 1987||The Colgate-Palmolive Co.||Free flowing high bulk density particulate detergent-softener|
|US4746445 *||Apr 7, 1986||May 24, 1988||Colgate-Palmolive Company||Process for manufacturing bentonite agglomerates|
|US4767546 *||Apr 7, 1986||Aug 30, 1988||Colgate-Palmolive Co.||Fabric softening bentonite agglomerates for use in laundry detergents|
|US4795032 *||Dec 4, 1987||Jan 3, 1989||S. C. Johnson & Son, Inc.||Wash-added, rinse-activated fabric conditioner and package|
|US4851137 *||May 4, 1988||Jul 25, 1989||Colgate-Palmolive Co.||Process for manufacturing bentonite agglomerates|
|US4970008 *||Dec 11, 1989||Nov 13, 1990||Kandathil Thomas V||Fabric conditioner comprising a mixture of quaternary ammonium compounds and select tertiary amines|
|US5019292 *||Dec 21, 1988||May 28, 1991||The Procter & Gamble Company||Detergent compositions|
|US5062972 *||Dec 20, 1989||Nov 5, 1991||The Procter & Gamble Co.||Fabric conditioning compositions: natural hectorite clay and binding and dispersing agent|
|US5470509 *||Sep 26, 1994||Nov 28, 1995||The Procter & Gamble Company||Low pH granular detergent composition having improved biodegradability and cleaning performance|
|US6462005 *||Jan 5, 1995||Oct 8, 2002||Texas Instruments Incorporated||Cleaning agent for a semiconductor device and a method of manufacturing a semiconductor device|
|US7989412||Aug 2, 2011||Henkel Ag & Co. Kgaa||Solid textile care composition based on soap|
|US20060034948 *||Oct 10, 2003||Feb 16, 2006||Sequoia Pacific Research Company, L.L.C.||Method for treating an environment that may be or is contaminated with an undesirable bacterial, virus and or spore|
|US20090099055 *||Oct 6, 2008||Apr 16, 2009||Henkel Ag & Co. Kgaa||Solid Textile Care Composition Based On Soap|
|USRE34062 *||Oct 3, 1984||Sep 15, 1992||Lever Brothers Company||Fabric softening composition contains water-insoluble surfactant and aliphatic mono-carboxylic acid|
|WO1993001267A1 *||Jun 24, 1992||Jan 21, 1993||The Procter & Gamble Company||Detergent compositions containing polyhydroxy fatty acid amide surfactants and a clay softening system|
|WO2002053692A1 *||Dec 13, 2001||Jul 11, 2002||Unilever Plc||Detergent compositions|
|WO2007115870A1 *||Mar 7, 2007||Oct 18, 2007||Henkel Ag & Co. Kgaa||Solid textile care composition based on soap|
|U.S. Classification||510/330, 510/443, 510/308, 510/482, 510/307, 510/469, 510/354, 510/515, 510/324, 510/504|
|International Classification||D06M13/322, D06M11/79, C11D3/12, C11D3/00, C11D1/62, C11D10/04, D06M13/192, D06M13/256, D06M13/02, D06M11/76, D06M11/72, D06M13/345, D06M13/46, C11D9/18, D06M11/00, D06M13/184, C09K3/16, C11D17/06, D06M13/262, D06M13/463, D06M23/08|
|Cooperative Classification||C11D10/047, C11D17/06, C11D3/001, C11D9/18, C11D1/62, C11D3/126|
|European Classification||C11D1/62, C11D9/18, C11D17/06, C11D10/04F, C11D3/00B3, C11D3/12G2D1|