|Publication number||US3886075 A|
|Publication date||May 27, 1975|
|Filing date||Apr 16, 1973|
|Priority date||Feb 16, 1973|
|Also published as||CA1022306A, CA1022306A1, CA1023505A, CA1023505A1, DE2406553A1, DE2406553C2, US3954632|
|Publication number||US 3886075 A, US 3886075A, US-A-3886075, US3886075 A, US3886075A|
|Inventors||Bernardino Lowell Watson|
|Original Assignee||Procter & Gamble|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (1), Referenced by (71), Classifications (35)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent Bernardino May 27, 1975 FABRIC SOFTENING COMPOSITION CONTAINING A SMECTITE TYPE CLAY  References Cited  Inventor: Lowell Watson Bernardino, T D T T S ATENTS Cincinnati, Ohio 3,644,203 2/1972 Lamberti et al. 252/8.8
73 A' :ThPt&GblC I Sslgnee f fsg e ompany Primary Examiner-Stephen J. Lechert, Jr.
Attorney, Agent, or Firm-Jack D. Schaeffer; Richard  Filed: Apr. 16, 1973 C. Witte; Thomas H. O'Flaherty  Appl. No.: 351,678
R l t d U S A l' t' D t  ABSTRACT a a Detergent-compatible fabric softening and anti-static  fgf g s g 'g of 337331 March compositions containing particular smectite clay matea an one rials, cationic anti-static agents and certain substituted amino compatibilizing agents are described. The com-  252/835 gg ggf o fi positions permit the simultaneous attainment of fabric [5 l 1 lm Cl noism 13/00 softening, static-reduction and cleansing effects of fab-  Field of Search 252/155, 8.75, 8.8, 546, washed 4 Claims, N0 Drawings 1 FABRIC SOFTENING COMPOSITION CONTAINING A SMECTITE TYPE CLAY CROSS REFERENCE TO RELATED APPLICATIONS This application is a continuation-in-part application of application Ser. No. 337,331, filed Mar. 2, 1973 now abandoned, titled: DETERGENT-COMPATIBLE FABRIC SOFTENING AND ANTI-STATIC COMPO- SITIONS, inventor Lowell W. Bernardino.
BACKGROUND OF THE INVENTION This invention related to compositions adapted to the provision of fabric softening and anti-static effects in fabric laundering operations. More particularly, it relates to the provision of these effects while simultaneous cleansing fabrics in the presence of conventional synthetic detergent compounds and organic or inorganic detergent builders.
Various clay materials have been utilized in many different types of detergent systems for widely diverse purposes. Clays, for example, have been disclosed for utilization as builders (Schwartz and Perry, Surface Active Agents, Interscience Publishers, Inc., 1949, pp. 232 and 299); as water-softeners (British Pat. No. 461,221); as anti-caking agents (US. Pat. Nos. 2,625,513 and 2,770,600); as suspending agents (US. Pat. Nos. 2,594,257, 2,594,258 and 2,920,045); and as fillers (US. 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 U.S. Pat. Nos. 3,033,699 and 3,594,221). The copending applications of Storm and Nirschl, Ser. No. 271,943, filed July 14, I972 now abandoned; Ohren, Ser. No. 279,127, filed Aug. 9, 1972, now US. Pat. No. 3,852,211 Nirschl and Gloss, Ser. No. 305,416, filed Nov. 10, 1972 now US. Pat. No. 3,862,058; and Gloss and Nirschl, Ser. No. 305,417, filed Nov. 10, 1972; relate to the use of clays as softeners in laundry compositions.
While clays can provide softening properties, and in the presence of detergent and builder substances used in the cleansing or laundering of fabrics, they do not provide anti-static properties. Commericallyacceptable fabric softeners additionally provide antistatic benefits, and such benefits have come to be expected by the user of such products. Indeed, fabrics coated with clays, while exhibiting a soft hand, tend to develop higher levels of static charge than the uncoated fabrics.
Various quaternary ammonium compounds known in the art possess anti-static properties. These compounds, while suitable in combination with clay materials to provide the anti-static properties which are not provided by the clays can be inhibited in their provision of anti-static effects by the presence of anionic substances conventionally employed in the cleansing of fabrics in laundering operations.
It is an object of the present invention to provide fabric softening and anti-static compositions capable of providing their effects in the presence of conventional detergent compositions to thereby concurrently launder, soften and impart anti-static benefits to fabrics.
It is another object of the present invention to provide compositions containing certain clay fabric softening agents and quaternary ammonium anti-static agents adapted to use in the washing cycle of a laundering operation.
These and the objects are obtained herein, as will be seen from the following disclosure.
SUMMARY OF THE INVENTION The present invention is based in part upon the discovery that certain substituted amino compounds, defined hereinafter, will mitigate the interactive effects of quaternary ammonium anti-static agents and conventional detergent laundering compositions. These materials, termed compatibilizing agents hereinafter, can be employed in combination with quaternary ammonium anti-static agents and clay fabric-softening materials in fabric-laundering operations to provide treated textile materials with simultaneous cleansing, anti-static and fabric-softening effects.
In its composition aspect, the present invention encompasses fabric-softening compositons containing as essential ingredients a particular smectite-type clay fabric-softening material, a quaternary ammonium fabric softening agent and a substituted amino compatibilizing agent. Such compositions can be conveniently employed by the housewife or other user by addition to the laundry washing bath provided by addition to water of a conventional laundry detergent composition. The present invention also encompasses as integral formulations compositions containing the materials hereinbefore-defined in combination with synthetic detergent compounds and organic or inorganic builder salts. Such compositions, merely added to water, provide in a single step the provision of a laundering bath adapted to the provision of simultaneous cleansing, softening and anti-static effects.
In a method aspect, the invention encompasses a method for simultaneously cleansing, softening and providing anti-static effects on fabrics or textiles which comprises treating the fabrics or textiles in an aqueous laundry bath containing detergent, clay, quaternary ammonium and compatibilizing agent as defined herein.
DETAILED DESCRIPTION OF THE INVENTION Compositions suited herein as additives to the detergent washing bath of a laundering operation, and termed additive compositions herein comprise:
a. from about 2 to about by weight of a smectitetype clay having an ion-exchange capacity of at least 50 meq/ I00 grams;
b. from about 1 to about 40% by weight of a substantially water-insoluble quaternary ammonium anti-static agent of the formula:
wherein R and R represent hydrocarbyl groups containing from about 10 to about 22 carbon atoms, R; and R represent hydrocarbyl groups containing from 1 to about 4 carbon atoms, X is an anion and n is an integer from I to 3; and
c. from about I to about 40% by weight of a compatibilizing agent of the formula:
wherein R, represents an alkyl group containing from 1 to about 22 carbon atoms; R and R represent alkyl groups containing from 1 to about 10 carbon atoms or hydrogen, whereby not more than one of the groups R and R can be hydrogen; and Y represents CONH CON(R or COOH, wherein R. represents a alkyl group containing from 1 to about 4 carbon atoms or hydrogen.
Built laundry detergent compositions of the invention comprise (a) from about 2 to about 30% by weight of a synthetic detergent compound selected from the group consisting of anionic soap and non-soap detergents, nonionic synthetic detergents, ampholytic synthetic detergents, zwitterionic synthetic detergents and mixtures thereof; (b) from about to about 60% by weight of an organic or inorganic detergent builder salt; (6) from about 1 to about 50 by weight ofa smectitetype clay softening agent having an ion exchange capacity of at least about SO/meq/lOO g; (d) from about 0.5 to about 15% by weight of a substantially waterinsoluble quaternary ammonium anti-static agent of the formula, R N*R' X wherein each R is an alkyl group containing from about to about 22 carbon atoms and each R; is an alkyl group containing from about 1 to about 4 carbon atoms and wherein X is an anion, e.g., F', Cl, Br', OH; and (e) from about 0.5 to about of an amino compound having the formula:
wherein R represents an alkyl group containing from 1 to about 22 carbon atoms; R and R represent alkyl groups containing from 1 to about 10 carbon atoms or hydrogen. whereby not more than one of the groups R and R can be hydrogen; and Y represnts CONH CON(R or -COOH, wherein R represents an alkyl group containing from about 1 to about 4 carbon atoms or hydrogen. The weight ratio of smectite typc clay-to-quaternary ammonium compound in the detergent compositions herein is from about 40:] to about 1:] and is preferably about 10:] to 3:1. The quaternary ammonium compound and amino compatibilizing agent are present in releasable combination in the com positions herein in a weight ratio of quaternary ammonium compound to amino compound of from about 1:5 to about 5:], preferably from 3:1 to 1:2.
The detergent compositions herein provide a solution pH of from about 7 to about 12 when dissolved in water at a concentration of about 0.12% by weight.
The compositions and method of this invention employ three essential ingredients; the clay softener; the quaternary ammonium anti-static agent; and the amino compatibilizing agent. The detergent compositions of the invention additionally will comprise a water-soluble detergency compound and a detergency builder salt. The smcctite-type clay functions to soften the laun dered fabrics while the quaternary ammonium compound provides anti-static effects on the fabrics and adds an increment of softening benefits to the fabrics. The detergent and builder components provide the known cieansing and building effects. The various components of the compositions herein are described in greater detail hereinafter.
CLAY COMPOUNDS The essential clay component of the present compo sitions consists of particular smectite clay materials. These smectite clays are present in the additive compositions of this invention at levels from about 2 to about 90%, preferably from 5 to 90% and especially from 8 to by weight. In the built detergent composition embodiments of this invention, the smectite clay is used in an amount from about 1 to about 50%, preferably from about 5 to about 25% by weight. The clays used herein are impaipable, i.e., have a particle size which cannot be perceived tactilely. lmpalpable clays have particle sizes below about 50 microns; the clays used herein have a particle size range of from about 5 microns to about 50 microns.
The clay minerals can be described as expandabie, three layer clays, i.e., alumino-silicates and magnesium silicates, having an ion exchange capacity of at least 50 rneq/lOO g. of clay. 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 (Si O (OH) and Mg (Si O )[OH) for the aluminum and magnesium oxide type clay, respectively. It is to be recognized 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 the 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++, as well as H+, 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-siiicates 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 inventon contain cationic counterions such as protons, sodium ions, potassium ions, caicium ion, magnesium ion, and the likev 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 (NHQ-l-NaOH Since the foregoing equilibrium reaction, one equivalent weight of ammonium ion replaces an equivalent weight of sodium, it is customary to measure cation ex change capacity (sometimes termed base exchange capacity) in terms of milli-equivalents per lOO g. of clay (Meq./l g.), The cation exchange capacity of clays can be measured in several ways, including by electodialysis, by exchange with ammonium ion followed by titration or by a methylene blue procedure, all as fully set forth in Grimshaw, The Chemistry and Physics of Clays", pp. 264-265, lnterscience (1971)v The cation exchange capacity of a clay mineral relates to such fac tors 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/lOO g. for kaolinites to about 150 meq/IOO g., and greater, for certain clays of the montmorillonite variety. lllite clays have an ion exchange capacity somewhere in the lower portion of the range, i.e., around 26 meq/lOO 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. However, smectites, such as nontronite, having an ion exchange capacity of approxmately 5O meq/lOO g., saponite, which has an ion exchange capacity of around 70 meq/lOO 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 in that they are deposited on the fabrics to provide the desired softening benefits. Accordingly, clay minerals useful herein can be characterized as expandable, three-layer smectite-type clays having an ion exchange capacity of at least about 50 meq/lOO g. A smectite-type clay known as fooler clay, found in a relatively thin vein above the Black Hills, also has the requisite ion exchange properties characteristic of the clays useful herein and such fooler clay is also encompassed by the term smectite-type clay, as used herein.
The smectite clays used in the compositions herein are all commercially available. Such clays include, for example, montmorillonite, volchonskoite, nontronite, hectorite, saponite, sauconite, and vermiculite. The clays herein are available under various tradenames, for example, Thixogel No. 1 (also, Thixoalell) and Gelwhite GP from Georgia Kaolin Co, Elizabeth, New Jersey; Volclay BC and Volclay No. 325, from American Colloid Co, Skokie, Illinois; Black Hills Bentonite Bl-l450, from international Minerals and Chemicals; and Veegum Pro and Veegum F, from R. T. Vanderbilt. It is to be recognized that such smectitc-type minerals obtained under the foregoing tradenames can comprise mixtures of the various discreet mineral enti ties. Such mixtures of the smectite minerals are suitable for use herein.
While any of the smectite-type clays having a cation exchange capacity of at least about 50 meq/lOO g. are useful herein, certain clays are preferred. For example, Gelwhite GP is an extremely white form of smectite smectite clay clay and is therefore preferred when formulating white granular detergent compositions. Volclay BC, which is a smectite-type clay mineral containing at least 3% of iron (expressed as Fe O in the crystal lattice, and which has a very high ion exchange capacity, is one of the most efficient and effective clays for use in the instant compositions and is preferred from the standpoint of product performance. On the other hand, certain smectite clays 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, taken in combination with exchange capacity measurements performed in the manner noted above, provides a basis for selecting particular smectite-type minerals for use in the compositions disclosed herein.
ANTI-STATIC AGENT The quaternary ammonium anti-static agents will normally be employed in the additive compositions in an amount of from about 1 to about 40% and preferably from about 2 to about 25% by weight. The quaternary ammonium anti-static agent will normally be present in the detergent compositions of the invention in an amount of from about 0.5 to about 15% and preferably in an amount of from about l to about l0% by weight. Whether an additive or detergent composition; of the invention is employed in providing an aqueous laundering bath or liquor, an amount sufficient to prqvide a concentration of quaternary ammonium compound in the bath or liquor offrom about 2.5 ppm (parts per million) to about 1500 ppm will normally be employed. ln general, the quaternary anti-stats are used in either type of composition at a clay-to-quaternary weight ratio of from about 40:1 to about l:l, preferably from about l0:l to about 3:l.
The anti-static agents useful herein 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 I to about 4 carbon atoms X in the above compounds can be any saltforming anion, e.g, halide, hydroxide, sulfate, carbonate, phosphate, etc. The charge on the anion is designated as n-, where n is 1-3. The number of cationic ammonium groups, n, will equal the charge, n, on the anion to provide electrical neutrality. Quaternary ammonium compounds wherein n=l 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. When the quaternary anti-static agent is affixed to the surface of the clay, it does not provide the desired anti-static effects on fabrics.
The quaternary ammonium antistatic agents used in this invention can be prepared in various ways well known in the art. Many such materials are commercially available. The quaternaries are often made from alkyl halide mixtures corresponding to the mixed alkyl chain lengths in fatty acids. For example, the di-tallow 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 counter-ion 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 ammo nium 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, chlo ride ion is the preferred counter-ion from a cost standpoint.
The following are representative examples of sub-- stantially 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 com pounds hereinafter is only by way of example and is not intended to be limiting of such compounds. Dioctadecyldimethylammonium chloride is an especially preferred quaternary anti static agent for use herein by virtue of its high anti-static activity; ditallow dimethyl ammonium chloride is equally preferred because of its readily availability and its good anti-static activity; other useful di-long chain quaternary com pounds are dicetyldimethylammonium chloride; bis-docosyldimethylammonium chloride; didodecyl dimethylammonium chloride; ditallowdimethylarnmonium bromide, dioleoyldimethylammonium hydroxide; ditallowdiethylammonium chloride; ditallowdipropylammonium bromide; ditallowdibutylammonium fluoride, cetyldecylmethylethylammonium choride. bis-[ditallowdimethylammonium]sulfatc; tris- [ditallowdimethylammonium]phosphate; and the like.
COMPATIBILIZING AGENT The essential amino compatabilizing agent is used is an amount of from about 1 to about 40%, preferably from about 2 to about 20% by weight of the ternary mixture of essential components, i.e., the additive compositions of the invention. In the built detergent embodiments, said compatiblizing agent is used in an amount from about 0.5 to about 15%, preferably from about 1 to about 10% by weight. Normally, in either the additive or detergent embodiments of the invention, an amount of amino compatibilizing agent sufficient to provide a weight ratio of quaternary ammonium compound to amino component of from about 5:1 to about 1:5, and preferably from 3:1 to 1:2, is employed.
The compatibilizing agent can be represented by substituted amino compounds having the formula:
wherein R, represents an alkyl group containing from 1 to about 22 carbon atoms; R and R represent alkyl groups containing from l to about 10 carbon atoms or hydrogen, whereby not more than one ofthe groups R and R; can be hydrogen; and Y represents -CONH CON(R,) or COOH; wherein R represents an alkyl group containing from 1 to about 4 carbon atoms or hydrogen.
Preferred herein because of ready availability and also by virtue ofits high anti-static activity is N-coco-B- amino-propionic acid.
Other useful compatibilizing agents include:
Octadecylamino-propionic acid Methylamino-bispropionamide Tallow alkyl-amino-dipropionic acid Dodecylamino-diacetic acid Hexadecylamino-bisacetamide Hexylamino-bisbutyramide Nhexadecyloaminoacetic acid Dodecyl-aminodiacetic acid N-octyl-B-amino acetamide Butylamino-pelargonamide Ethylamino-dicaproamide Methylamino-din-heptylamide DETERGENT from the group consisting of anionic, nonionic, am-
pholytic and zwitterionic detergents and mixtures thereof. Examples of organic detergents of these types are described in us. Pat. NO. 3,579,454; incorporated herein by reference. column 11, line 45 to column 19, line 64.
Preferred for use herein are the water-soluble salts of alkyl benzene sulfonates, in which the alkyl group contains from about 9 to about 20 carbon atoms in straight chain or branched chain configuration, e.g., those of the type described in US. Pat. Nos. 2,220,099 and 2,477,383 (especially valuable are linear straight chain alkyl benzene sulfonates in which the average of the alkyl groups is about 1 1.8 carbon atoms and commonly abbreviated as C,, LAS). Suitable cations include alkali me als (sodium. potassium, lithium) ammonium and substituted ammonium (mono, di and tri-ethanol and methanol amines) neutralizing agents.
Another preferred detergent for use herein include alkyl ether sulfates. These materials have the formula RO(C H, O) SO M wherein R is alkyl or alkenyl of about 10 to about 20 carbon atoms, x is l to 30, and M is a watensoluble cation such as alkali metal, ammonium and substituted ammonium. The alkyl ether sulfates useful in the present invention are condensation products of ehtylene oxide and monohydric alcohols having about i() to about 20 carbon atoms. Preferably, R has 14 to 18 carbon atoms. The alcohols can be derived from fats, cg, 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 1 to 6, molar proportions of ethylene oxide and the resulting mixture of molecular species, having, for example, an average of 3 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; sodium tallow alkyl trioxyethylene ether sulfate; and sodium tallow alkyl hexaoxyethylene sulfate.
Other preferred detergents utilizable herein 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 in conditions such that any sultones which have been formed in the reaction are hydrolyzed to give the corresponding hydroxy-alkane-sulfonates. The sulfur trioxide can be liquid or gaseous, and is usually, but not necessarily, diluted by inert diluents, for example by liquid S chlorinated hydrocarbons, etc., when used in the liquid form, or by air, nitrogen, gaseous S0 etc., when used in the gaseous form.
The oz-olefins from which the olefin sulfonates are derived are mono-olefins having 12 to 24 carbon atoms, preferably 14 to l6 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 portion of hydroxy-alkanesulfonates, the olefin sulfonates can contain minor amounts of other materials, such as alkene disulfonates depending upon the reaction conditions, proportion of reactants, the nature of the starting olefins and impurities in the olefin stock and side reactions during the sulfonation process.
A specific anionic detergent which has also been found excellent for use in the present invention is described more fully in the U.S. Pat. No. 3,332,880 of Phillip F. Pflaumer and Adrian Kessler, issued July 25, i967, titled Detergent Composition", the disclosure of which is incorporated herein by reference.
Builder Salts The detergent compositions of the instant invention contain, as an essential component, an alkaline, polyvalent anionic detergent builder salt. in the present compositions these water-soluble alkaline builder salts serve to maintain the pH of the laundry solution in the range of from about 7 to about 12, preferably from about 8 to about ll. Furthermore, these builder salts enhance the fabric cleaning performance of the overall compositions while at the same time serve to suspend particulate soil released from the surface of the fabrics and prevent its redeposition on the fabric surfaces. Surprisingly, although the detergency builder salts serve to suspend clay soils of the kaolinite and illite types and prevent their redeposition on fabrics, they do not appear to interfere with the deposition on fabric surfaces of the smectite-type clay softeners used herein. Furthermore, these polyanionic builder salts have been found to cause the smectite-type clays present in the granular detergent formulations of the invention to be readily and homogeneously dispersed throughout the aqueous laundering medium with a minimum of agitation. The homogeneity of the clay dispersion is necessary for the clay to function effectively as a fabric softener, while the ready dispersability allows granular detergent compositions to be formulated.
Suitable detergent builder salts useful herein can be of the poly-valent inorganic and poly-valent organic types, or mixtures thereof. Non-limiting examples of suitable water-soluble, inorganic alkaline detergent builder salts include the alkali metal carbonates, borates, phosphates, polyphosphates, tripolyphosphates, bicarbonates, silicates and sulfates. Specific examples of such salts include the sodium and potassium tetraborates, perborates, bicarbonates, carbonates, tripolyphosphates, orthophosphates and hexametaphosphates.
Examples of suitable organic alkaline detergency builder salts are: (l) water-soluble amino polyacetates, e.g., sodium and potassium ethylenediaminetetraacetates, nitrilotriacetates and N-( 2-hydroxyethyl)nitrilodiacetates; (2) water-soluble salts of phytic acid, e.g., sodium and potassium phytates; (3) water-soluble polyphosphonates, including, sodium, potassium and lithium salts of ethane-lhydroxy-l,l-diphosphonic acid; sodium, potassium and lithium salts of methylenediphosphonic acid and the like.
Additional organic builder salts useful herein include the polycarboxylate materials described in US. Pat. No. 2,264,l03, including the water-soluble alkali metal salts of mellitic acid. The water-soluble salts of polycarboxylate polymers and copolymers such as are described in US. Pat. No. 3,308,067, incorporated herein by reference, are also suitable herein. It is to be understood that while the alkali metal salts of the foregoing inorganic and organic poly-valent anionic builder salts are preferred for use herein from an economic standpoint, the ammonium, alkanolammonium, e.g., triethanolammonium, diethanolammonium, and the like, water-soluble salts of any of the foregoing builder anions are useful herein.
Mixtures of organic and/or inorganic builders can be used herein. One such mixture of builders is disclosed in Canadian Pat. No. 755,038, c.g., a ternary mixture of sodium tripolyphosphate, trisodium nitrilotriacetate and trisodium ethane-l -hydroxy-l ,l-diphosphonate.
While any of the foregoing alkaline poly-valent builder materials are useful herein, sodium tripolyphosphate, sodium nitrilotriacetate, sodium mellitate, sodium citrate and sodium carbonate are preferred herein for this builder use. Sodium tripolyphosphate is especially preferred herein as a builder both by virtue of its detergency builder activity and its ability to homogeneously and quickly disperse the smectite clays throughout the aqueous laundry media without interfering with clay deposition on the fabric surface. Sodium tripolyphosphate is also especially effective for suspending illite and kaolinite clay soils and retarding their redeposition on the fabric surface.
The detergent builders are used at concentrations of from about 0 to about 60%, preferably 20 to 50%, by weight of the detergent compositions of this invention.
The clay-containing compositions of this invention are in granular form. The compositions can be conveniently prepared in standard fashion by admixing the clay and detergent, builder and optional ingredients, if any, in a crutcher anad spray-drying the mixture to form granules.
Following this, the quaternary ammonium anti-static agent and amino compatibilizing agent can be sprayed on the granules from a melt. It is a critical aspect of this invention to avoid affixing the quaternary compound to the surface of the clay by an ion exchange mechanism; accordingly, it is preferable to avoid spraying the detergent granules with an aqueous solution or suspension of the quaternary compound. The ion-exchange problem is avoided by employing a melt of the quaternary compound and at least a portion of the amino compatibilizing agent to spray onto the granules. The compositions are then added to water. or to a detergent bath as the case may be, to provide a laundering liquor. Soiled fabties are added to the laundering liquor and cleansed in the usual manner. The effective amount of the additive or detergent compositions to be used will depend to an extent on the weight of clothes being laundered and their degree of soiling. Aqueous laundering baths prepared thereby provide adequate cleaning, softening and anti-static benefits with soiled fabrics, especially cotton and cotton/polyester blends.
It will be appreciated that the method of simultaneously cleansing, softening and reducing static buildup on laundered textiles can be conveniently practiced by providing an aqueous treating liquor in a number of ways. A suitable washing liquor can be prepared by adding, for example, a commercially-available built anionic-based laundry detergent composition into a wash ing machine at a concentration of about 0.12% and separately. adding an additive composition of the invention as defined hereinbefore. Suitable treating liquors will normally contain:
Smectite clay S to 5000 ppm Quaternary ammonium compound 25 to 1500 ppm Amino computibilizing agent 2.5 to 1500 ppm Detergent 10 to 3000 ppm; and Builder to 6000 ppm, whereby the weight ratio of quaternary ammonium compound to amino compatibilizing component is normally in the range from about to about l;5.
The additive and built detergent compositions and processes of the instant invention are illustrated by the following examples.
EXAMPLE I A through-the-wash cycle fabric-softening detergent composition which imparts imultaneous cleansing, softening and anti-static properties to fabrics treated therewith having the following formula is prepared:
Component Weight Percent Anionic surfactant* 16.6 Sodium tripolyphosphate 43.3 Sodium silicate 5.8 Sodium sulfate 10.0 Gelwhite GP (smectite) 9.8 Dioctadecyl dimethyl ammonium chloride 2.0 N'coco-B-amino propionic acid Miscellaneous minors" ca. 3. Moisture Balance l ZI'I ratio of sodium tallow alkyl sulfate-sodium C linear alkyl benzene sulfonatc "Including hnghtcncrs. curboxymethylcellulose, coconut alcohol cthoxylutc and perfume sulfate; sodium coconut alkyl ethylene glycol ether sulfate; sodium tallow alkylhexaoxyethylene sulfate; olefin sulfonates produced by means of uncomplexed sulfur trioxyde sulfonation of l-dodecene; l-tetradecene; l hexadecene; l-octadecene; l-eicosene and ltetracosene and sodium linear dodecyl benzene sulfonate.
Substantially similar detergency, softening and antistatic benefits are obtained when the clay softening agent in Example I is replaced with an equivalent amount of volchonskoit, nontronite; nectorite; sauconite; and vermiculite, respectively, all such clays having an ion exchange capacity of at least about 50 meq,/
EXAMPLE II Through-thc-wash-cycle fabric softener additive compositions having the following formulas are prepared:
Components Formula (IN parts) Sodium bicarbonate 7 l3 Ditallow dimethyl ammonium chloride 8 4 N-cocoflhmino propionic acid 4 2 Sodium montmorillonite 21 2] Extender granules* 60 60 Parts *Sodium linear dodeeyl benzene sulfonate 6 Sodium silicate solids (ratio SiO (N3 0 2.0) 12 Sodium carbonate 12 Sodium sulfate 23 Minors 2 When employed in conjunction with a commerciallyavailable anionic-based built detergent composition in a conventional laundering process, the foregoing additive composition provides fabric softening and antistatic effect.
The extender granules employed in the composition of Example ll are replaced with any inert or compatible filler materials such as sodium, sulfate, starch, or the like with similar results.
EXAMPLE III A through-the-wash cycle fabric-sfotener composition having the following formula is prepared:
Silicate solids (ratio siO fNa O 2.0)
Balance to 86 Moisture and minor ingredients The composition of Example III when used in a conventional laundry operation at a product concentration 15 of 0.12% by weight provides fabric-softening, cleansing and anti-static benefits which are substantially similar to what can be obtained from a conventional laundry operation in combination with the subsequent rinsesoftening treatment.
What is claimed is:
l. A fabric softening composition comprising:
a. from about 2 to about 90% by weight of a smectitetype clay having an ion-exchange capacity of at least 50 meq/lOO grams;
b. from about 1 to about 40% by weight of a substantially water-insoluble quaternary ammonium antistatic agent of the formula:
wherein R and R represent hydrocarbyl groups containing from about 10 to about 22 carbon atoms, R and R represent hydrocarbyl groups containing from l to about 4 carbon atoms, X is an anion and n is an integer from i to 3; and
c. from about i to about 40% by weight of a compatibilizing agent of the formula:
wherein R represents an alkyl group containing from l to about 22 carbon atoms; R and R represent alkyl groups containing from i to about 10 carbon atoms or hydrogen, whereby not more than one of the groups R and R can be hydrogen; and Y represents CONH CON(R or COOH; wherein R represents an alkyl group containing from 1 to about 4 carbon atoms or hydrogen.
2. A composition in accordance with claim 1 wherein the component (a) smectite-type clay is used in an amount from about 5 to about 90% by weight.
3. A composition in accordance with claim 2 wherein the component (b) quaternary ammonium component is present in an amount from about 2 to about 25% by weight.
4. A composition in accordance with claim 3 wherein the component (a) smectite-type clay is used in an amount from about 8 to about by weight.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3644203 *||Dec 9, 1968||Feb 22, 1972||Lever Brothers Ltd||Fabric softener|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4055248 *||Aug 12, 1976||Oct 25, 1977||The Procter & Gamble Company||Fabric treating compositions and articles|
|US4073996 *||Feb 24, 1976||Feb 14, 1978||The Procter & Gamble Company||Fabric treating articles and processes|
|US4178255 *||May 15, 1978||Dec 11, 1979||Colgate-Palmolive Company||Detergent compositions|
|US4183815 *||May 15, 1978||Jan 15, 1980||Colgate-Palmolive Company||Laundry detergent compositions|
|US4292035 *||Nov 20, 1978||Sep 29, 1981||The Procter & Gamble Company||Fabric softening compositions|
|US4338204 *||Sep 22, 1980||Jul 6, 1982||The Procter & Gamble Company||Detergent softener containing anionic, amine, and water soluble cationic|
|US4375416 *||Oct 16, 1980||Mar 1, 1983||The Procter & Gamble Company||Detergent composition having textile softening properties|
|US4536315 *||Jun 1, 1983||Aug 20, 1985||Colgate Palmolive Co.||Perfume-containing carrier having surface-modified particles for laundry composition|
|US4536316 *||Jun 1, 1983||Aug 20, 1985||Colgate-Palmolive Co.||Fabric softening composition containing surface modified clay|
|US4661289 *||Aug 27, 1985||Apr 28, 1987||Lever Brothers Company||Detergent compositions|
|US4764292 *||Oct 5, 1987||Aug 16, 1988||Lever Brothers Company||Fabric-softening particles|
|US4830784 *||Mar 2, 1987||May 16, 1989||Henkel Kommanditgesellschaft Auf Aktien||Laundry detergents and cleaners with reduced requirement for conventional chemicals|
|US4844824 *||Feb 8, 1988||Jul 4, 1989||The Procter & Gamble Company||Stable heavy duty liquid detergent compositions which contain a softener and antistatic agent|
|US4851138 *||Sep 2, 1987||Jul 25, 1989||Akzo, N.V.||Fabric softening composition and detergent-composition comprising the same|
|US4863523 *||Apr 3, 1987||Sep 5, 1989||Henkel Kommanditgesellschaft Auf Aktien||Process for cleaning soiled solid molded articles|
|US4913828 *||Jun 10, 1987||Apr 3, 1990||The Procter & Gamble Company||Conditioning agents and compositions containing same|
|US4915854 *||Oct 15, 1987||Apr 10, 1990||The Procter & Gamble Company||Ion-pair complex conditioning agent and compositions containing same|
|US4960526 *||Oct 3, 1989||Oct 2, 1990||Colgate-Polmolive Company||Diammonium compound containing fabric softening and antistatic detergent composition|
|US5004556 *||Apr 21, 1989||Apr 2, 1991||Colgate-Palmolive Company||Built thickened stable non-aqueous cleaning composition and method of use|
|US5019280 *||Feb 8, 1989||May 28, 1991||The Procter & Gamble Company||Ion-pair complex conditioning agent with benzene sulfonate/alkyl benzene sulfonate anionic component and compositions containing same|
|US5073274 *||Apr 30, 1990||Dec 17, 1991||The Procter & Gamble Co.||Liquid detergent containing conditioning agent and high levels of alkyl sulfate/alkyl ethoxylated sulfate|
|US5445747 *||Aug 5, 1994||Aug 29, 1995||The Procter & Gamble Company||Cellulase fabric-conditioning compositions|
|US5466394 *||Apr 25, 1994||Nov 14, 1995||The Procter & Gamble Co.||Stable, aqueous laundry detergent composition having improved softening properties|
|US5599786 *||Aug 12, 1993||Feb 4, 1997||The Procter & Gamble Company||Cellulase fabric-conditioning compositions|
|US5616553 *||Aug 12, 1993||Apr 1, 1997||The Procter & Gamble Company||Fabric conditioning compositions|
|US5622925 *||Nov 8, 1995||Apr 22, 1997||The Procter & Gamble Company||Stable, aqueous laundry detergent composition having improved softening properties|
|US5721205 *||Mar 12, 1997||Feb 24, 1998||The Procter & Gamble Company||Cellulase fabric-conditioning compositions|
|US5919745 *||Jul 11, 1997||Jul 6, 1999||Church & Dwight Co., Inc||Liquid laundry detergent composition containing nonionic and amphoteric surfactants|
|US5968203 *||Feb 26, 1998||Oct 19, 1999||Sybron Chemicals Inc.||Clay-containing textile material treating composition and method|
|US5972049 *||Jan 28, 1998||Oct 26, 1999||Sybron Chemicals Inc.||Clay-containing dispersing composition for carriers used in the disperse dyeing of hydrophobic textiles|
|US6645569||Jan 30, 2002||Nov 11, 2003||The Procter & Gamble Company||Method of applying nanoparticles|
|US6818610||Jul 16, 2002||Nov 16, 2004||Procter & Gamble Company||Fabric care systems for providing anti-wrinkle benefits to fabric|
|US6863933||Jan 30, 2002||Mar 8, 2005||The Procter And Gamble Company||Method of hydrophilizing materials|
|US6872444||Jan 30, 2002||Mar 29, 2005||The Procter & Gamble Company||Enhancement of color on surfaces|
|US7112621||Jan 30, 2002||Sep 26, 2006||The Proctor & Gamble Company||Coating compositions for modifying surfaces|
|US7196048||Jul 21, 2004||Mar 27, 2007||The Procter & Gamble Co.||Fabric care systems for providing anti-wrinkle benefits to fabric|
|US7441599||Nov 18, 2005||Oct 28, 2008||Chevron U.S.A. Inc.||Controlling the pressure within an annular volume of a wellbore|
|US7510005||Dec 21, 2007||Mar 31, 2009||Chevron U.S.A. Inc.||Controlling pressure and static charge build up within an annular volume of a welllbore|
|US7743830||Oct 10, 2008||Jun 29, 2010||Chevron U.S.A. Inc.||Controlling the pressure within an annular volume of a wellbore|
|US7870905||Mar 12, 2010||Jan 18, 2011||Chevron U.S.A. Inc.||Controlling the pressure within an annular volume of a wellbore|
|US7950460||Dec 17, 2009||May 31, 2011||Chevron U.S.A. Inc.||Controlling the pressure within an annular volume of a wellbore|
|US7963333||Dec 17, 2009||Jun 21, 2011||Chevron U.S.A. Inc.||Controlling the pressure within an annular volume of a wellbore|
|US9506015||Nov 21, 2014||Nov 29, 2016||Ecolab Usa Inc.||Compositions to boost fabric softener performance|
|US9688945||Nov 21, 2014||Jun 27, 2017||Ecolab Usa Inc.||Compositions to boost fabric softener performance|
|US9725679||Nov 21, 2014||Aug 8, 2017||Ecolab Usa Inc.||Compositions to boost fabric softener performance|
|US20020151634 *||Jan 30, 2002||Oct 17, 2002||Rohrbaugh Robert Henry||Coating compositions for modifying surfaces|
|US20020192366 *||Jan 30, 2002||Dec 19, 2002||Cramer Ronald Dean||Method of hydrophilizing materials|
|US20030096728 *||Jul 16, 2002||May 22, 2003||The Procter & Gamble Company||Fabric care systems for providing anti-wrinkle benefits to fabric|
|US20040052957 *||Sep 16, 2003||Mar 18, 2004||Cramer Ronald Dean||Method of applying nanoparticles|
|US20040259762 *||Jul 21, 2004||Dec 23, 2004||The Procter & Gamble Company||Fabric care systems for providing anti-wrinkle benefits to fabric|
|US20060119128 *||Nov 18, 2005||Jun 8, 2006||Aero Industries, Inc.||Dual tarp cover system|
|US20070114034 *||Nov 7, 2006||May 24, 2007||Chevron U.S.A. Inc.||Controlling pressure and static charge build up within an annular volume of a wellbore|
|US20080223576 *||Dec 21, 2007||Sep 18, 2008||Chevron U.S.A. Inc.||Controlling pressure and static charge build up within an annular volume of a wellbore|
|US20090133878 *||Oct 10, 2008||May 28, 2009||Chevron U.S.A. Inc.||Controlling the Pressure Within an Annular Volume of a Wellbore|
|US20100096138 *||Dec 17, 2009||Apr 22, 2010||Chevron U.S.A. Inc.||Controlling the Pressure Within an Annular Volume of a Wellbore|
|US20100163236 *||Dec 17, 2009||Jul 1, 2010||Chevron U.S.A. Inc.||Controlling the Pressure Within an Annular Volume of a Wellbore|
|US20100236780 *||Mar 12, 2010||Sep 23, 2010||Chevron U.S.A. Inc.||Controlling the Pressure within an Annular Volume of a Wellbore|
|CN101346530B||Nov 16, 2006||Jun 27, 2012||璐彩特国际公司||Controlling pressure and static charge within a wellbore|
|CN102261230B||Nov 16, 2006||Jun 4, 2014||雪佛龙美国公司||Controlling the pressure within an annular volume of a wellbore|
|CN102305046B||Nov 16, 2006||Feb 26, 2014||雪佛龙美国公司||Controlling the pressure within an annular volume of a wellbore|
|DE102007012909A1||Mar 19, 2007||Sep 25, 2008||Momentive Performance Materials Gmbh||Mit Duftstoffen modifizierte, reaktive Polyorganosiloxane|
|DE102007012910A1||Mar 19, 2007||Sep 25, 2008||Momentive Performance Materials Gmbh||Mit Duftstoffen modifizierte, verzweigte Polyorganosiloxane|
|EP0011340A1 *||Nov 8, 1979||May 28, 1980||THE PROCTER & GAMBLE COMPANY||Detergent composition having textile softening properties|
|EP0146289A2 *||Nov 29, 1984||Jun 26, 1985||THE PROCTER & GAMBLE COMPANY||Laundry compositions|
|EP0146289B1 *||Nov 29, 1984||Jun 2, 1993||THE PROCTER & GAMBLE COMPANY||Laundry compositions|
|EP0164797A2 *||May 30, 1985||Dec 18, 1985||THE PROCTER & GAMBLE COMPANY||Fabric softener agglomerates|
|EP0164797A3 *||May 30, 1985||Jun 28, 1989||The Procter & Gamble Company||Fabric softener agglomerates|
|EP0760243A1||Aug 31, 1995||Mar 5, 1997||THE PROCTER & GAMBLE COMPANY||Use of allylic alcohol perfumes as a malodour reduction agent|
|EP0839899A1||Oct 30, 1996||May 6, 1998||THE PROCTER & GAMBLE COMPANY||Fabric softening compositions|
|EP2947138A1||Jun 1, 2007||Nov 25, 2015||The Procter & Gamble Company||Concentrated perfume compositions|
|WO2008057102A1 *||Nov 16, 2006||May 15, 2008||Chevron U.S.A. Inc.||Controlling pressure and static charge within a wellbore|
|U.S. Classification||510/515, 510/330|
|International Classification||D06M11/79, D06M13/322, D06M11/00, D06M13/463, D06M13/46, C11D3/12, D06M13/342, C11D3/26, D06M13/402, D06M13/02, D06M13/192, D06M13/345, D06M13/184, C11D3/20, C11D3/00, D06M13/207, D06M13/188|
|Cooperative Classification||C11D3/26, D06M13/46, C11D3/2075, C11D1/10, C11D3/126, C11D3/001, D06M13/342, D06M13/402|
|European Classification||C11D1/10, D06M13/402, D06M13/342, C11D3/26, C11D3/12G2D1, D06M13/46, C11D3/00B3, C11D3/20E|