WO2001041910A2

WO2001041910A2 - Process for preparing ether-capped poly(oxyalkylated) alcohol surfactants

Info

Publication number: WO2001041910A2
Application number: PCT/US2000/033350
Authority: WO
Inventors: Mark Robert Sivik; Glenn Thomas Jordan, Iv; Bernard William Kluesener
Original assignee: The Procter & Gamble Company
Priority date: 1999-12-08
Filing date: 2000-12-08
Publication date: 2001-06-14
Also published as: CA2391956A1; EP1235778A2; WO2001041910A3; MXPA02005741A; JP2003516367A; AU2075901A

Abstract

A process for preparing an ether-capped poly(oxyalkylated) alcohol surfactant is provided. The alcohol has the formula: RO(R10)xCH(CH3)OR2 wherein, R is selected from the group consisting of linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from about 1 to about 30 carbon atoms; R1 may be the same or different, and is independently selected from the group consisting of branched or linear C¿2? to C7 alkylene in any given molecule; x is a number from 1 to about 30; and R?2¿ is selected from the group consisting of: (i) a 4 to 8 membered substituted, or unsubstituted heterocyclic ring containing from 1 to 3 hetero atoms; and (ii) linear or branched, saturated or unsaturated, substituted or unsubstituted, cyclic or acyclic, aliphatic or aromatic hydrocarbon radicals having from about 1 to about 30 carbon atoms; provided that when R2 is (ii) then either at least one of R1 is other than C¿2? to C3 alkylene or R?2¿ has from 6 to 30 carbons atoms.

Description

PROCESS FOR PREPARING ETHER-CAPPED POL Y(OXY ALKYLATED)

ALCOHOL SURFACTANTS Technical Field The present invention relates to a process for preparing low-foaming nonionic surfactants and more particularly to a process for preparing ether-capped poly(oxyalkylated) alcohol surfactants which have superior spotting and filming benefits in dishwashing and hard surface cleaning applications, as well as suds suppression in detergent compositions.

Background of the Invention Due to the varied nature of different cleaning compositions, different surfactants are better suited for some applications while being less suited or totally unsuitable for other applications. Nonionic surfactants, such as alcohol ethoxylates, and alkyl glucose amides are of considerable importance in detergent products. For example, under some conditions, nonionic surfactants aid cleaning of greasy soils and inhibit the formation of calcium soap. However, conventional nonionic surfactants designed for effective cleaning in laundry products form liquid crystalline phases on mixing with water. These phases can hinder the rate of mixing with water and lead to undesirable optical properties of thin films on solution drying. For example, conventional nonionics sprayed on the surface of granules to achieve target density can give rise to poor granule dissolution and residue in horizontal axis machine dispensers. Conventional nonionics formulated at high levels in liquid products can lead to poor rates of mixing with water and consumer concern. Conventional nonionics in window and floor cleaners can form visible liquid crystalline films on drying that increase the effort required by the consumer to achieve good results. Similarly, a nonionic surfactant for use in an automatic dishwashing machine would need to minimize foam production and not leave undesirable spots and films on the cleaned surfaces.

On account of the foregoing technical constraints as well as consumer needs and demands, product compositions are undergoing continual change and improvement.

Moreover environmental factors such as the need for biodegradable materials, the restriction of phosphate, the desirability of providing ever-better cleaning results with less product, providing less thermal energy demand, and less water to assist the washing process, have all driven the need for improved compositions.

Accordingly, the need remains for new surfactants which are suitable for use in a variety of compositions which can provide improve dissolution of solid products (like bars and tablets) and granular products, improved rates of mixing with water as with liquid products, improved streaking and filming performance as in hard surface cleaners and automatic dishwashing, good cleaning, suds control and good biodegradability while avoiding incompatibility with other cleaning surfactants and/or bleach.

BACKGROUND ART U.S. Patent 4,272,394, WO 94/22800, WO 93/04153, WO96/00253 and WO

98/17379.

SUMMARY OF THE INVENTION In accordance with a first aspect of the present invention, a process for preparing an ether-capped poly(oxyalkylated) alcohol surfactant is provided. The surfactant has the formula:

wherein, R is selected from the group consisting of linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from about 1 to about 30 carbon atoms; R¹ may be the same or different, and is independently selected from the group consisting of branched or linear C₂ to C alkylene in any given molecule; x is a number from 1 to about 30; and R² is selected from the group consisting of:

(i) a 4 to 8 membered substituted, or unsubstituted heterocyclic ring containing from 1 to 3 hetero atoms; and (ii) linear or branched, saturated or unsaturated, substituted or unsubstituted, cyclic or acyclic, aliphatic or aromatic hydrocarbon radicals having from about 1 to about 30 carbon atoms; provided that when R² is (ii) then either at least one of R¹ is other than C to C alkylene or R has from 6 to 30 carbon atoms. The process comprises the steps of:

(a) providing a vinyl ether of the formula R OCH<Η₂ wherein R is as defined above;

(b) providing an alkoxylated alcohol of the formula

RO(R'O)_xH wherein R, R¹, and x, are as defined above;

(c) reacting said vinyl ether with said alkoxylated alcohol in the presence of a catalyst to form said ether-capped poly(oxyalkylated) alcohol.

These and other aspects, features and advantages will become apparent to those of ordinary skill in the art from a reading of the following detailed description and the appended claims. All percentages, ratios and proportions herein are by weight, unless otherwise specified. All temperatures are in degrees Celsius (° C) unless otherwise specified. All documents cited are in relevant part, incorporated herein by reference. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Once again, the present invention is directed toward a process for producing a low- foaming nonionic surfactant for use in detergent compositions.

It has been surprisingly discovered in accordance with the present invention that significant improvements in spotting and filming characteristics and, when used in conjunction with high cloud point surfactants, in the removal of greasy soils relative to conventional surfactants, are provided via the ether-capped poly(oxyalkylene) alcohol surfactants of the present invention.

The novel surfactants of the present invention comprise ether-capped poly(oxyalkylated) alcohols having the formula:

In one aspect of the present invention R is a linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic hydrocarbon radical having from about 1 to about 20 carbon atoms, even more preferably R is a linear or branched, saturated, aliphatic hydrocarbon radicals having from about 4 to about 18 carbon atoms.

In one aspect of the present invention R, R¹ and R² are selected such that the ether-capped poly(oxyalkylated) alcohol surfactant contains one or more chiral carbon atoms. In the novel compounds of the present invention, when R² is (ii) then either at least one of R is other than C to C₃ alkylene or R has from 6 to 30 carbon atoms. That

9 • • 9 is, when R is (ii), R is either linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from about 6 to about 30 carbon atoms or linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from about 1 to about 30 carbon atoms, with at least one of R¹ is other than C₂ to C alkylene. For example, when R² is a hydrocarbon of the formula:

— (CH₂)_y -X where, y and X are described hereafter, or R² is a hydrocarbon radical of the formula:

— C(CH₃)₂R³ where, R³ is described hereafter, then at least one of R¹ is other than C₂ to C₃ alkylene. For example, if x is 5, and R² was (CH )_y-X, then the ether-capped poly(oxyalkylated) alcohol could have the formula:

RO(CH₂CH(CH₂CH₃)O)₅CH(CH₃)O— (CH₂)_y - X or RO(CH₂CH₂O)₄(CH₂CH(CH₂CH₃)O)CH(CH₃)O— (CH₂)_y - X or RO(CH₂CHCH₃O)(CH2CH(CH2CH₃)O)4CH(CH₃ — (CH₂)_y - X

9 "

Similarly, for example if R was -C(CH₃)₂R and x was 7, then the ether-capped poly(oxyalkylated) alcohol could have the formula:

RO(CH₂CH₂O)₆(CH₂CH₂(CH₂CH₃)O)CH(CH₃)O — C(CH₃)₂R³ or

RO(CH₂CHCH₃O)₄(CH₂CH(CH₂CH₃)O)₃CH(CH₃)O— C(CH₃)₂R³ or

RO(CH2CH₂θ)₃(CH2CHCH₃0)2(CH₂CH(CH₂CH₃)0)(CH₂CH(CH2CH₂CH₃)0)CH(CH₃)0— C(CH₃)₂R

These examples are included merely for illustrative purposes and are not to be construed in any manner as limiting of the scope of the present invention. In one aspect of the present invention, R is a hydrocarbon radical of the formula: R⁴ R⁵ R⁶

I I I

CH₃(CH₂)_qCH(CH₂)_rCH(CH₂)_sCH(CH₂)_tCH₂— wherein R^, R-\ and R" are each independently selected from hydrogen, and Cj-C alkyl, , more preferably hydrogen, C1 -C2 alkyl, even more preferably hydrogen, and methyl, provided that R^, R5, and R" are not all hydrogen and, when t is 0, at least R^ or R^ is not hydrogen; q, r, s, t are each independently integers from 0 to 13. In one more preferred form of this aspect R is selected from the formulas:

CH₃ CH₃(CH₂)_nCH(CH₂)_mCH₂-

CH₃ CH₃

CH₃(CH₂)_JCH(CH₂)_kCHCH₂— wherein n, m, j and k are each independently integers from 0 to 13. In one aspect of the present invention R is a hydrocarbon radical of the formula:

— C(CH₃)₂R³

R³ is selected from the group consisting of linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from about 1 to about 30, more preferably 1 to 20, even more preferably 1 to 15, carbon atoms,. In one embodiment of this aspect of the present invention, R³ is ethyl.

In one aspect of the present invention R is a 4 to 8 membered substituted, or unsubstituted heterocyclic ring containing from 1 to 3 hetero atoms. In one embodiment of this aspect of the invention the hetero atoms are selected from the group comprising oxygen, nitrogen, sulfur and mixtures thereof. In one embodiment of this aspect of the invention R² is a 5 or 6 member heterocycle. In another embodiment of this aspect of the present invention R² is selected from the group consisting of:

wherein each R is independently selected from the group consisting of hydrogen, linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic hydrocarbon or alkoxy radical having from about 1 to about 10 carbon atoms, or R⁷ is a saturated or unsaturated, substituted or unsubstituted, alicyclic or aromatic hydrocarbon radical having, from about 1 to about 10 carbon atoms, which is fused to the heterocyclic ring; each A is independently selected from the group consisting of O, and N(R⁸)_a, wherein R⁸ is independently selected from the group consisting of hydrogen, linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic hydrocarbon radical having from about 1 to about 10 carbon atoms, and a is either 0 or 1 ; z is an integer from 1 to 3.

In another embodiment of this aspect of the present invention R² is selected from the group consisting of:

wherein R⁷ is defined as above.

wherein R⁷ and R⁸ are defined as above.

In another embodiment of this aspect of the present invention R is selected from the group consisting of:

In one aspect of the present invention R is a 7 to 13 membered substituted, or unsubstituted polycyclic ring. In one embodiment of this aspect of the present invention R² is selected from the group consisting of substituted, or unsubstituted adamantane, substituted, or unsubstituted norbornane, substituted, or unsubstituted nortricyclene, and substituted, or unsubstituted bicyclo[2.2.2]octane. In another embodiment of this aspect of the present invention R is a substituted, or unsubstituted adamantane.

In one aspect of the present invention R is a hydrocarbon of the formula:

— (CH₂)_y - X wherein, y is an integer from 0 to 7, X, is a 4 to 8 membered substituted, or unsubstituted, saturated or unsaturated cyclic or aromatic hydrocarbon radical. In another embodiment of this aspect of the present invention y is an integer from 1 to 2, and X is selected from the group consisting of to 5 to 8 membered substituted, or unsubstituted, aromatic hydrocarbon radical.

In another embodiment of this aspect of the present invention y is 0 and X, is a 5 or 6 membered substituted, or unsubstituted, saturated or unsaturated cyclic or aromatic hydrocarbon radical.

In another embodiment of this aspect of the present invention X is selected from the group consisting of:

wherein each R⁹ is independently selected from the group consisting of hydrogen, linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic hydrocarbon or alkoxy radical having from about 1 to about 10 carbon atoms, or R⁹ is a saturated or unsaturated, substituted or unsubstituted, alicyclic or aromatic hydrocarbon radical having, from about 1 to about 10 carbon atoms, which is fused to the ring; w is an integer from 1 to 3.

wherein R is defined as above.

In one aspect of the present invention R is a linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from about 1 to about 30 carbon atoms, more preferably R is a linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic hydrocarbon radical having from about 1 to about 20 carbon atoms, even more preferably R² is a linear or branched, saturated, aliphatic hydrocarbon radicals having from about 4 to about 18 carbon atoms.

In one aspect of the present invention, when x is greater than 2, R¹ may be the same or different. That is, R¹ may vary between any of the alkyleneoxy units as described above. For instance, if x is 3, R¹ may be selected to form ethlyeneoxy(EO) or propyleneoxy(PO) and may vary in order of (EO)(PO)(EO), (EO)(EO)(PO);

(EO)(EO)(EO); (PO)(EO)(PO); (PO)(PO)(EO) and (PO)(PO)(PO). Of course, the integer three is chosen for example only and the variation may be much larger with a higher integer value for x and include, for example, multiple (EO) units and a much small number of (PO) units. Similarly, ethylene, and propylene are chosen for example only and the variation may be much larger with selection of linear or branched butylene, pentylene, hexylene and or heptylene.

The surfactants of the present invention can be prepared via a variety of different processes. In one aspect of the present invention, the surfactants may be prepared by reacting a vinyl ether of the formula:

R²OCH=CH₂ wherein R is as defined above; with an alkoxylated alcohol of the formula

RO(R'O)_xH wherein R, R¹, and x, are as defined above, in the presence of a catalyst to form the ether- capped poly(oxyalkylated) alcohol.

In one embodiment of this aspect of the present invention the step of reacting of vinyl ether with alkoxylated alcohol is conducted in the presence of a catalyst. Suitable catalysts include Lewis acids; acids and their salts, both organic and inorganic; pyridinium salts; polymers; clays, such as, Spanish sepiolite clay, GIRDLER K-10; aluminosilicates or zeolites, such as HZS-360 zeolite, H-Y zeolite; activated carbon, such as sulfonated charcoal; transition metal complexes, such as, molybedenyl(NI) acetylacetone; transition metal salts, such as lanthum trichloride, eerie ammonium nitrate; 2,3-dichloro-5,6,dicyano-p-benzoquinone; bis(trimethysilyl)sulfate, and mixtures thereof.

Suitable Lewis acids include, but are not limited to, TiCl Ti(O¹Pr)4, ZnCl2, SnCl2, AICI3, platinum dichloride, copper(II) chloride, phosphorous pentachloride, phosphorous trichloride, cobalt(II) chloride, zinc oxide, iron(II) chloride and BF3-OEt2-

Suitable inorganic acids include, mineral acids, such as, phosphoric acid, sulfuric acid, hydrochloric acid, phosphorous oxychloride, aluminium phosphate and ammonium chloride. Furthermore, the mineral acids or their salts can optionally be adsorbed on to a substrate, such as, silica gel, or alumina. For example sulfuric acid adsorbed on silica gel, or alumina impregnated with zinc chloride.

Suitable organic acids include: carboxylic acids, such as, acetic acid, oxalic acid, glycolic acid, citric acid, tartaric acid, maleic acid and oxydisuccinic acid; halogenated carboxylic acids, such as, trifluoroacetic acid, heptafluorobutyric acid, dichloroacetic acid, and trichloroacetic acid; and sulfonic and sulfinic acids and their salts such as, p- toluenesulfonic acid, p-toluenesulfinic acid, methanesulfonic acid, trifluoromethanesulfonic acid, 4-bromobenzene sulfonic acid, naphthalene sulfonic acid, (+)-10-camphor sulfonates, and alkyl benzene sulfonic acid.

Suitable pyridinium salts, include, but are not limited to, pyridinium p- toluenesulfonate (PPTS), pyridinium p-toluenesulfinate, pyridinium hydrochloride, pyridinium hydrobromide, pyridinium hydrogen bisulfate, pyridinium hydrogen sulfate and mixtures thereof.

Suitable transition metal, include, but are not limited to, molybedenyl(VI) acetylacetone; transition metal salts, such as lanthum trichloride, eerie ammonium nitrate; 2,3-dichloro-5,6,dicyano-p-benzoquinone, mercury(II) acetate, mercury(II) trifluroacetate, copper(II) acetylacetonate and tetracarbonylbis(cyclopentadienyl)diiron.

Suitable polymers, include, but are not limited to, polymeric ion exchange resins, or polyvinyl pyridines. Suitable polymeric ion exchange resins include those of the Amberylst series, such as AMBERYLST®15, available from Rohm & Haas, the DOWEX® series, such as, DOWEX 50X8-50 available from Dow; REILLEX 424, available from Reilly Industries; the Amberlite series, such as AMBERLITE IRA-400, or AMBERLITE IR-1 18, available from Rohm & Haas; available from United Catalyst ; the ENVIROCAT series, such as ENNIROCAT EPZG, available from Contract Chemicals; and combinations thereof. Suitable polyvinyl pyridines can be unsubstituted or substituted, such as substituted on the vinyl group and/or on the pyridine ring. Examples of suitable polyvinyl pyridines include, but are not limited to, poly(4-vinylpyridine trifluoromethanesulfonate), poly(2-vinylpyridine trifluoromethanesulfonate), poly(4- vinylpyridine p-toluenesulfonate), poly(2-vinylpyridine p-toluenesulfonate), poly(4- vinylpyridine chloride), poly(2-vinylpyridine chloride), poly(4-vinylpyridine bromide), poly(2-vinylpyridine bromide), and mixtures thereof. These polymeric catalysts have the additional advantage of being easy to separate from the surfactant produced.

Other suitable catalysts include, bis(trimethysilyl)sulfate, iodotrimethylsilane, allytrimethyl silane, hexamethyldisilane, iodine, bromine, iron(II) sulfate, triphenylphosphine, aluminium sulfate, alkylether sulfuric acids, alkyl sulfuric acids, lithium perchlorate, lithium tetrafluoroborate, acetonyltriphenylphosphonium bromide, zirconium hydroxide, potassium cyanide, and platinum oxide. Preferred catalysts include the sulfonic acids, Lewis acids, polyvinyl pyridines, methanesulfonic acid, AMBERYLST®15, acidic versions of DOWEX® and pyridinium p-toluenesulfonate (PPTS) with polyvinyl pyridines, pyridinium p-toluenesulfonate

(PPTS), p-toluenesulfonic acid, DOWEX®, AMBERYLST®15 and methanesulfonic acid, being the most preferred.

Mixtures of catalysts are also within the scope of the present invention. Similarly, the uses of supported, such as in a column for a continuous reaction, and unsupported catalysts are also within the scope of the present invention.

The catalysts are preferably employed at amounts of about 0.1 mol % to about 20.0 mol %, more preferably from about 0.1 mol % to about 10.0 mol %, even more preferably from about 0.1 mol % to about 5.0 mol %, even more preferably still from about 0.1 mol % to about 2.0 mol %, even more preferably still from about 0.2 mol % to about 1.0 mol %. Other suitable catalysts can be found in US patent No. U.S. Patent 4,272,394, and in PCT publications, WO 94/22800, WO 93/04153, WO96/00253 and WO 98/17379 all of which are incorporated herein by reference.

In one embodiment of this aspect of the present invention the reaction is conducted in the presence of a solvent, or mixtures of solvents. It is preferred that the solvent be a polar aprotic solvent. Suitable solvents include, but are not limited to, hexane, benzene, toluene, xylene, mesitylene, dichloromethane, tetrahydrofuran, dioxane, chloroform, diethylether, methyl tert-butylether, acetone, acrylonitrile, or the like. Furthermore, the reaction is preferably conducted at temperatures ranging from about - 20°C to about 300°C, and more preferably from about -10°C to about 250°C. Lastly, the reaction is preferably conducted at pressures ranging from about 0.5 atmospheres to about 100 atmospheres, and more preferably from about 0.8 atmospheres to about 10 atmospheres.

In another embodiment of this aspect of the present invention the step of reacting vinyl ether with alkoxylated alcohol is conducted in the absence of a solvent.

Further disclosure on suitable solvents and catalysts can be found in "Advanced

Organic Chemistry", by Jerry March, 4^th ed., Wiley-Interscience, 1992, "Comprehensive Organic Transformations" by Richard C. Larock, VCH Publishers, 1989, and "Protective

Groups in Organic Synthesis" 3^RD ed. by Theodora W. Greene and Peter G. M. Wuts, Wiley-Interscience, 1999 the relevant portions of which are incorporated herein by reference.

In one embodiment of the present invention, the process is performed as a batch process. That is, the reaction is let proceeded to completion, or near completion, and then final product is removed. In another embodiment of the present invention, the process is performed as a continuous process. That is, the product of the process is continuously removed from the reaction vessel while staring material is added at a comparable rate.

In one embodiment of the present invention the vinyl ether is reacted with the alkoxylated alcohol at a mole ratio of from about 5 to about 1 , more preferably from about 3 to about 1 , more preferably still from about 1.5: 1 to about 0.90: 1 mole %.

In one embodiment of the process of the present invention the process may be conducted in an inert gas. This may be done by sparging with any suitable inert gas, such as nitrogen, helium, neon, or argon.

In one embodiment of the present invention reaction step (c) may be followed by optional step (d). Step (d), is a step in which the reaction step (c) is quenched, preferably by the addition of base. The amount of the ether capped poly(oxyalkylated) alcohol surfactant present in the reaction mixture will depend upon many factors, including but not limited to, starting materials, temperature, catalyst selection and the like. Quenching stops the reaction, of the starting materials, and ensures that any ether capped poly(oxyalkylated) alcohol surfactant produced does not undergo further reaction or revert back to the starting materials. The quenching of step (c) produces a mixture which contains ether capped poly(oxyalkylated) alcohol surfactant, as well as, unreacted starting materials, catalyst and the products of any side reactions. In one embodiment of this present invention the quenching of the reaction of step (c) is done when the reaction mixture preferably contains at least 90%, more preferably 95% by weight of ether capped poly(oxyalkylated) alcohol surfactant. The remaining 10%, more preferably 5% by weight, comprises, unreacted starting material as well as products of side reactions, such as byproduct acetals. In one aspect of this embodiment of the present invention the base may be optionally selected from the group consisting of alkali metal carbonates, alkali metal bicarbonates alkali metal hydroxides, alkali metal alcoholates, alkanolamines, alkylamines, aromatic amines and mixtures thereof. In a further aspect of the present invention the base may be optionally selected from the group consisting of potassium carbonate, sodium carbonate, sodium bicarbonate sodium methoxylate, sodium ethoxylate, potassium tert-butyloxylate, triethylamine, triethanolamine and mixtures thereof. In another aspect of this embodiment of the present invention the base may be in the form of an aqueous solution. In a further aspect of this embodiment of the present invention the aqueous solution may be at a temperature of from about 20°C to about 60°C.

The expression "product of step (c)" is meant to include not only the ether-capped poly(oxyalkylated) alcohol surfactant but also any unreacted starting materials or any materials produced from side reactions, such as dimers, which would be present at the conclusion of step (c).

In one embodiment of the present invention the process of the present invention may optionally further comprise a step (e). Step (e) is removal of color bodies and/or odors from the product of steps (c), or (d). In one aspect of this embodiment of the present invention removal of the color bodies and/or odors is obtained by contacting the product of steps (c) or (d) with a reagent. The reagent can either be an oxidant, or a reductant. Suitable oxidants include hydrogen peroxide. Suitable reductants include sodium borohydride, and hydrogen over a palladium/carbon catalyst. In a further aspect of this embodiment of the present invention the color bodies and/or odors are removed by contacting the product of steps (c) or (d) first with an oxidant and then a reductant or first with a reductant and then an oxidant.

In one embodiment of the present invention the ether-capped poly(oxyalkylated) alcohol surfactant produced in step (c) may optionally removed from the product of step (c) by centrifuging. Some representative examples of this synthetic route of this aspect of the invention is demonstrated via the following diagrams.

CH₃(CH₂)₈CH₂(OCH₂CH2)₇θH ^■

The ether-capped poly(oxyalkylated) alcohol surfactant product is then collect by means common in the art such as extraction. If desired, the surfactant may be further treated by stripping, distillation or various other means before use. The surfactants made by the process disclosed herein may contain related impurities which will not adversely affect performance.

PROCESS EXAMPLES Example 1

Preparation of C _{1 1} H₂ EO₇BO₂-2-ethylhexyl acetal

Neodol 1-7 (20.00 g, 41.6 mmol) is placed into a 500 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at 75°C. After releasing the vacuum with argon, sodium metal (0.05 g, 2.1 mmol) is added and the mixture stirred for 1 h at 120°C. After increasing the reaction temperature to 140°C, 1 ,2-epoxybutane (6.00 g, 83.2 mmol) is added dropwise over 30 minutes. After the addition is complete the mixture is stirred for an additional 1 h at 140°C. The solution is cooled to 90°C and neutralized with concentrated HCl. After removing water and the last traces of 1 ,2-epoxybutane under vacuum and cooling to ambient, methylene chloride (200 ml) and 2-ethylhexyl vinyl ether (19.49 g, 124.7 mmol) are added. The mixture is cooled to 0°C and pyridinium /?-toluenesulfonate (0.42 g, 1.7 mmol) is added. The mixture is first stirred 4 h at 0°C and then 18 h at ambient. After diluting with diethyl ether (200 ml), the mixture is washed twice with saturated sodium bicarbonate and the organic layer dried with sodium sulfate/potassium carbonate. The product was concentrated by rotary evaporation and dried under vacuum in the presence of potassium carbonate to yield a yellow liquid. Example 2

Examples 2(a) to (i) are illustrative of some of the possible catalysts, work up options and relative amounts the starting materials that can be used in the present invention. Example 2(a)

Preparation of C₉ πHi₉/₂₃Eθ₈-cyclohexyl acetal

Neodol 91-8 (20.00 g, 39.1 mmol) is placed into a 250 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at 75 °C. After cooling to ambient and releasing the vacuum with argon, methylene chloride (100 ml) and cyclohexyl vinyl ether (5.43 g, 43.01 mmol) are added. The mixture is cooled to 0°C and pyridinium p-toluenesulfonate (0.43 g, 1.6 mmol) is introduced into the flask. The mixture is first stirred 4 h at 0°C and then 18 h at ambient. The product mixture is then washed twice with saturated sodium bicarbonate and the organic layer dried over sodium carbonate, concentrated by rotary evaporation and further stripped under vacuum at 60°C (0.1 mmHg) in the presence of potassium carbonate to yield a liquid. Example 2(b)

Preparation of C_9/nHi₉/₂ EO₈-cyclohexyl acetal

Neodol 91-8 (20.00 g, 39.1 mmol) and poly(4-vinylpyridinium p-toluenesulfonate) (0.43 g) are introduced into a 250 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at

75°C. After cooling to ambient and releasing the vacuum with argon, cyclohexyl vinyl ether (4.94 g, 39.1 mmol) is added. The mixture is heated to 70-95°C overnight. The product mixture is filtered to yield a liquid. Example 2(c)

Preparati on of C₉/ 11 H _19/23EO₈-cyclohexy 1 acetal

Neodol 91-8 (20.00 g, 39.1 mmol) and poly(4-vinylpyridinium p-toluenesulfonate) (0.43 g) are introduced into a 250 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at 75°C. After cooling to ambient and releasing the vacuum with argon, cyclohexyl vinyl ether (4.94 g, 39.1 mmol) is added. The mixture is heated to 70-95°C overnight. The product mixture is separated from the catalyst by centrifugation to yield a liquid. Example 2(d)

Preparation of C_9/nHi_9/23EO₈-cyclohexyl acetal Neodol 91 -8 (20.00 g, 39.1 mmol) and poly(4-vinylpyridinium p-toluenesulfonate) (0.43 g) are introduced into a 250 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at 75°C. After cooling to ambient and releasing the vacuum with argon, cyclohexyl vinyl ether (4.94 g, 39.1 mmol) is added. The mixture is heated to 70-95°C overnight. The product mixture is washed with 20% potassium carbonate solution, dried and filtered to yield a liquid. Example 2(e)

Preparation of C_8/ioHi_7/2iEO₈-cyclohexyl acetal Alcohol ethoxylate C₈/ιoHι_{7 2}ιEθ8 (20.00 g, 40.2 mmol) and poly(4-vinylpyridinium chloride) (2.0 g) are introduced into a 250 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at 75°C. After cooling to ambient and releasing the vacuum with argon, cyclohexyl vinyl ether (5.07 g, 40.2 mmol) is added. The mixture is heated to 70-95°C overnight. The product mixture is filtered to yield a liquid. Example 2(f)

Preparation of C9/nHi9/₂ EO₈-cyclohexyl acetal

Neodol 91-8 (20.00 g, 39.1 mmol) and poly(4-vinylpyridinium p-toluenesulfonate) (7.82 g) are introduced into a 250 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at 75°C. After cooling to ambient and releasing the vacuum with argon, acetone (150 mL) and cyclohexyl vinyl ether (4.94 g, 39.1 mmol) are added. The mixture is stirred for three days, filtered and concentrated by rotary evaporation to yield a liquid. Example 2(g)

Preparation of C_9/1 iHi_9/23EO₈-cyclohexyl acetal

Neodol 91-8 (20.00 g, 39.1 mmol) is placed into a 250 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at 75°C. After cooling to ambient and releasing the vacuum with argon, methylene chloride (100 ml) and cyclohexyl vinyl ether (4.84 g, 38.4 mmol) are added. The mixture is cooled to 0°C and pyridinium p-toluenesulfonate (0.39 g, 1.5 mmol) is introduced into the flask. The mixture is first stirred 4 h at 0°C and then 18 h at ambient. The product mixture is then washed twice with saturated sodium bicarbonate and the organic layer dried over sodium carbonate, concentrated by rotary evaporation and further stripped under vacuum at 60°C (0.1 mmHg) in the presence of potassium carbonate to yield a liquid. Example 2(h)

Preparation of

acetal

Neodol 91-8 (20.00 g, 39.1 mmol) is placed into a 250 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at 75°C. After cooling to ambient, cyclohexyl vinyl ether (5.04 g, 39.9 mmol) is added. /?-Toluenesulfonic acid monohydrate (0.112 g, 0.59 mmol) is added to the mixture and stirred to dissolve. An exotherm is observed starting from 22°C and ending at 30°C, with the development of a precipitate. After 16 minutes of reaction time, the reaction pH is adjusted to >7 with triethanolamine, filtered and then stripped in a Kugelrohr oven (50°C, 0.1 mm Hg) to yield a quantitative amount of a near colorless liquid.

Example 2(i)

Preparation of C9 nHi₉/₂₃EO₈-cyclohexyl acetal

Neodol 91-8 (900.0 g, 1.76 mol) is placed into a 3 L three-necked rounded bottomed flask, fitted with a heating mantel, mechanical stirrer, internal thermometer, and vacuum argon take-off adapter. The contents are dried under vacuum at 80 °C for 30 min. A portion of the dry Neodol 91-8 (20 g) is set aside after the contents are cooled to room temperature. Cyclohexylvinyl ether (217.82 g, 1.73 mol) is then added to the reaction mixture. The reagents are cooled to about 10 °C at which point methanesulfonic acid (1.80 mL) and the 20 g portion of Neodol set aside are combined and added to the reaction mixture via syringe, subsurface, in one portion. The reaction mixture exotherms, ice bath controlled, to 22 °C. After lh, the mixture is quenched with 15% sodium carbonate solution (35 mL). The mixture is placed under vacuum by stripping in a Kugelrohr oven (25 °C, 0.1 mm Hg) for 10 min. The product is filtered to yield a quantitative amount of a near colorless liquid.

Example 3

Preparation of

acetal

The procedure of Example 2(i) is repeated with the substitution of Neodol 91-8 for

Neodol 1-7.

Example 4

Preparation of C₉/nHi_{9 3}EOs-benzyl acetal

The procedure of Example 3 is repeated with the substitution of benzyl vinyl ether for cyclohexyl vinyl ether.

Preparation of C 11 /i H? /₃1 EO i ?-2-ethylhexyl acetal

The procedure of Example 2(i) is repeated with the substitution of 2-ethylhexyl vinyl ether for cyclohexyl vinyl ether and Tergitol- 15-S- 12 for Neodol 1-7.

Example 6

Preparation Cn/i₅H₂₃/_{3 ]}EO9PO₂-cyclohexyl acetal

The procedure of Example 1 is repeated with the substitution of propylene oxide for 1 ,2- epoxybutane, cyclohexyl vinyl ether for 2-ethylhexyl vinyl ether, and Tergitol 15-S-9 for Neodol 1-7.

Example 7

Preparation of Cι_2/ι₅H_25/31EO₉BO₁ -cyclohexyl acetal

The procedure of Example 1 is repeated with the substitution of cyclohexyl vinyl ether for 2-ethylhexyl vinyl ether and Neodol 25-9 for Neodol 1-7. Example 8

Preparation of CnH₂₃EO₇-cyclohexyl acetal Neodol 1-7 (50.00 g, 104.0 mmol) is placed into a 1000 ml three-necked round-bottomed flask, fitted with a heating mantle, magnetic stirrer, internal thermometer and argon inlet and dried under vacuum at 75°C. After cooling to ambient and releasing the vacuum with argon, methylene chloride (500 ml) and cyclohexyl vinyl ether (6.55g, 51.9 mmol) are added. The mixture is cooled to 0°C and pyridinium /?-toluenesulfonate (1.04 g, 4.2 mmol) is introduced into the flask. The mixture is first stirred 4 h at 0°C and then 18 h at ambient. The product mixture is then washed twice with saturated sodium bicarbonate and the organic layer dried with magnesium sulfate, concentrated by rotary evaporation and further stripped under vacuum at 60°C (0.1 mmHg) to yield a liquid. Example 9

Preparation of Cn/ι₅H_23/3ιEOι₅-cyclohexyl acetal

Tergitol 15-S-15 (100.0 g, 193.8 mmol) is placed into a 250 ml three-necked round- bottomed flask, fitted with a heating mantel, magnetic stirrer, internal thermometer, and vacuum/argon take-off adapter. The contents are dried under vacuum at 80 °C for 10 min. A portion of the dry Tergitol 15-S-15 (2 g) is set aside after the contents are cooled to room temperature. Cyclohexyl vinyl ether (24.21 g, 191.9 mmol) is then added to the reaction mixture. The reagents are cooled to about 15 °C at which point methanesulfonic acid (0.28 g, 2.9 mmol) and the 2 g portion of Tergitol 15-S-15 set aside are combined and added to the reaction mixture via syringe, subsurface and in one portion. The reaction mixture exotherms to 40 °C. After 5 minutes, the reaction pH is adjusted to >7 with 15% sodium carbonate. The mixture is placed under vacuum by stripping in a Kugelrohr oven (50 °C, 0.1 mm Hg) for 10 min. The product is filtered to yield a quantitative amount of a near colorless liquid. The following examples are illustrative of the present invention, but are not meant to limit or otherwise define its scope. The ether-capped poly(oxyalkylated) alcohol surfactant produced by the process of the present invention may be used in other applications, such as a wetting agents, antifoaming agents, drilling muds, etc., in a wide range of fields, such as in biocides, pharmaceuticals, etc. Further examples of possible application for these surfactants can be found in "Nonionic Surfactants" edited by Martin J. Schinck, Surfactant Science Series, Mancel Dekker, NY, Volume 1; "Nonionic Surfactants: Physical Chemistry" edited by Martin J. Schinck, Surfactant Science Series, Mancel Dekker, NY, Volume 23; "Nonionic Surfactants: Polyoxyalkylen Block Copolymers" edited by Vaughn M. Nace, Surfactant Science Series, Mancel Dekker, NY, Volume 60; and L.G. Lundsted and I.R. Schmolka, in "Block and Graft Copolymerization", Vol. 2 (R.J. Ceresa, ed.), John Wiley & Sons, Ltd., London, 1976, pp.113-272. All parts, percentages and ratios used herein are expressed as percent weight unless otherwise specified. FORMULATION EXAMPLES

In the following Examples, the abbreviations for the various ingredients used for the compositions have the following meanings.

LAS Sodium linear C12 alkyl benzene sulfonate MBAS_X Mid-chain branched primary alkyl (average total carbons = x) sulfate MBAE_XS_Z Mid-chain branched primary alkyl (average total carbons = z) ethoxylate (average EO = x) sulfate, sodium salt MBAE_X Mid-chain branched primary alkyl (average total carbons = x) ethoxylate (average EO = 8)

TFAA C 16- 18 alkyl N-methyl glucamide

CxyEzS Sodium Cι_x-Cι_v branched alkyl sulfate condensed with z moles of ethylene oxide CxyFA C 1 _X-C 1 _v fatty acid CxyEz A Cι_x_iy branched primary alcohol condensed with an average of z moles of ethylene oxide C24 N-Me Glucamide C12-C14 N-methyl glucamide

CxAPA Alkyl amido propyl amine Citric acid Anhydrous citric acid Carbonate Anhydrous sodium carbonate with a particle size between 200μm and 900μm

Citrate Tri-sodium citrate dihydrate of activity 86.4% with a particle size distribution between 425μm and 850 μm Protease Proteolytic enzyme of activity 4KNPU/g sold by NOVO

Industries A/S under the tradename Savinase

Cellulase Cell lytic enzyme of activity 1000 CEVU/g sold by NOVO

Industries A S under the tradename Carezyme Amylase Amylolytic enzyme of activity 60KNU/g sold by NOVO

Industries A/S under the tradename Termamyl 60T Lipase Lipolytic enzyme of activity lOOkLU/g sold by NOVO Industries

A/S under the tradename Lipolase Endolase Endoglunase enzyme of activity 3000 CEVU/g sold by NOVO

Industries A/S PB1 Anhydrous sodium perborate bleach of nominal formula

NaBO₂.H2O

NOBS Nonanoyloxybenzene sulfonate in the form of the sodium salt. DTPMP Diethylene triamine penta (methylene phosphonate), marketed by Monsanto under the Trade name Dequest 2060

MEA Monoethanolamine

PG Propanediol

EtOH Ethanol

Brightener 1 Disodium 4,4'-bis(2-sulphostyryl)biphenyl Brightener 2 Disodium 4,4'-bis(4-anilino-6-mo holino-1.3.5-triazin-2- yl)amino) stilbene-2:2'-disulfonate. Silicone antifoam Polydimethylsiloxane foam controller with siloxane-oxyalkylene copolymer as dispersing agent with a ratio of said foam controller to said dispersing agent of 10:1 to 100:1.

NaOH Solution of sodium hydroxide DTPA Diethylene triamine pentaacetic acid

NaTS Sodium toluene sulfonic acid

Fatty Acid (C 12/14) C12-C14 fatty acid

Fatty Acid (TPK) Topped palm kernel fatty acid

Fatty Acid (RPS) Rapeseed fatty acid Borax Na tetraborate decahydrate

PAA Polyacrylic Acid ( w = 4500)

PEG Polyethylene glycol (mw=4600)

MES Alkyl methyl ester sulfonate

SAS Secondary alkyl sulfate NaPS Sodium paraffin sulfonate

C45AS Sodium C14-C15 linear alkyl sulfate

CxyAS Sodium Cj_x-Ciy alkyl sulfate (or other salt if specified) AQA R2.N⁺(CH3)_x((C₂H₄O)yH)z with R2 = Cg - Cig where x +z = 3, x = 0 to 3, z = 0 to 3, y = 1 to 15. STPP Anhydrous sodium tripolyphosphate

Zeolite A Hydrated Sodium Aluminosilicate of formula

Nai2(A102Siθ2)i2- 27H2O having a primary particle size in the range from 0.1 to 10 micrometers

NaSKS-6 Crystalline layered silicate of formula δ -Na2Si2θ5 Bicarbonate Anhydrous sodium bicarbonate with a particle size distribution between 400μm and 1200μm

Silicate Amoφhous Sodium Silicate (SiO2:Na2O; 2.0 ratio)

Sulfate Anhydrous sodium sulfate PAE ethoxylated tetraethylene pentamine PIE ethoxylated polyethylene imine PAEC methyl quaternized ethoxylated dihexylene triamine

MA/AA Copolymer of 1 :4 maleic/acrylic acid, average molecular weight about 70,000.

CMC Sodium carboxymethyl cellulose Protease Proteolytic enzyme of activity 4KNPU/g sold by NOVO

Industries A/S under the tradename Savinase

Cellulase Cellulytic enzyme of activity 1000 CEVU/g sold by NOVO

Industries A/S under the tradename Carezyme Amylase Amylolytic enzyme of activity 60KNU/g sold by NOVO

Industries A/S under the tradename Termamyl 60T Lipase Lipolytic enzyme of activity 1 OOkLU/g sold by NOVO Industries

A/S under the tradename Lipolase

Percarbonate Sodium Percarbonate of nominal formula 2Na2CO3.3H2O2 NaDCC Sodium dichloroisocyanurate TAED Tetraacetylethylenediamine DTPMP Diethylene triamine penta (methylene phosphonate), marketed by

Monsanto under Tradename Dequest 2060

Photoactivated bleach Sulfonated Zinc Phthalocyanine bleach encapsulated in dextrin soluble polymer

HEDP 1 , 1 -hydroxyethane diphosphonic acid SRP 1 Sulfobenzoyl end capped esters with oxyethylene oxy and terephthaloyl backbone

SRP 2 sulfonated ethoxylated terephthalate polymer

SRP 3 methyl capped ethoxylated terephthalate polymer

Isofol 16 Condea trademark for C16 (average) Guerbet alcohols

CaC12 Calcium chloride

MgC12 Magnesium chloride

DTPA Diethylene triamine pentaacetic acid

EXAMPLES lOA to 10E: Nonaqueous Liquid Laundry Detergent compositions Non-limiting examples of bleach-containing nonaqueous liquid laundry detergent are prepared as follows.

Preparation of LAS Powder for Use as a Structurant Sodium C12 linear alkyl benzene sulfonate (NaLAS) is processed into a powder containing two phases. One of these phases is soluble in the non-aqueous liquid detergent compositions herein and the other phase is insoluble. It is the insoluble fraction which serves to add structure and particle suspending capability to the non-aqueous phase of the compositions herein.

NaLAS powder is produced by taking a slurry of NaLAS in water (approximately 40-50% active) combined with dissolved sodium sulfate (3-15%) and hydrotrope, sodium sulfosuccinate (1-3%). The hydrotrope and sulfate are used to improve the characteristics of the dry powder. A drum dryer is used to dry the slurry into a flake. When the NaLAS is dried with the sodium sulfate, two distinct phases are created within the flake. The insoluble phase creates a network structure of aggregate small particles (0.4-2 um) which allows the finished non-aqueous detergent product to stably suspend solids.

The NaLAS powder prepared according to this example has the following makeup shown in Table I.

TABLE I

LAS Powder

Non-aqueous based heavy duty liquid laundry detergent compositions which comprise the capped nonionic surfactants of the present invention are presented below.

The resulting compositions are stable, anhydrous heavy-duty liquid laundry detergents which provide excellent rates of mixing with water as well as good stain and soil removal performance when used in normal fabric laundering operations.

EXAMPLE 1 1 : Hand Dishwashing Liquid compositions

The following examples further illustrate the invention herein with respect to a hand dishwashing liquid. Ingredient % (wt.) Range (% wt.)

Nonionic from example 8 5.0 1 - 20 MBAE Si5 2.0 0.5-10

Ammonium C 12-13 alkyl sulfate 7.0 2-35

Cl2"Ci4 ethoxy (1) sulfate 20.5 5-35

Coconut amine oxide 2.6 2-5

Betaine/Tetronic 704®** 0.87-0.10 0-2 (mix) Alcohol Ethoxylate Cg.\ 1E9 1.0 0.5-10

Ammonium xylene sulfonate 4.0 1-6 Ethanol 4.0 0-7

Ammonium citrate 0.06 0-1.0 Magnesium chloride 3.3 0-4.0 Calcium chloride 2.5 0-4.0 Ammonium sulfate 0.08 0-4.0 Perfume 0.18 0-0.5

Maxatase® protease 0.50 0-1.0 Water and minors Balance —

** Cocoalkyl betaine. EXAMPLES 12 to 16: Shampoo compositions

Example Number

Component 12 13 14 15 16

Ammonium laureth-2 sulfate 5 3 2 10 8

Ammonium lauryl sulfate 5 5 4 5 8 Nonionic from example 3 2 0 0 4 7

Nonionic from example 6 0 3 0 0 0

Nonionic from example 7 0 0 4 1 0

Cocamide MEA 0 0.68 0.68 0.8 0

PEG 14M 0.1 0.35 0.5 0.1 0

Cocoamidopropylbetaine 2.5 2.5 0 0 1.5

Cetylalcohol 0.42 0.42 0.42 0.5 0.5

Stearylalcohol 0.18 0.18 0.18 0.2 0.18

Ethylene glycol distearate 1.5 1.5 1.5 1.5 1.5

Dimethicone * 1.75 1.75 1.75 1.75 2.0

Perfume solution 0.45 0.45 0.45 0.45 0.45

DMDM hydantoin 0.37 0.37 0.37 0.37 0.37

Color solution (ppm) 64 64 64 64 64

Water and minors q. s. to 100%

1. Dimethicone is a 40(gum)/60(fluid) weight ratio blend of SE-76 dimethicone gum available from General Electric Silicones Division and a dimethicone fluid having a viscosity of 350 centistokes.

EXAMPLES 17 to 32: Granular Laundry Detergents

The following laundry detergent compositions are prepared in accord with the invention:

EXAMPLES 33 to 40: Hard Surface Cleaners

Mixing the listed ingredients in the listed proportions made the following compositions. These compositions were used neat to clean marble and dilute to clean lacquered wooden floors. Excellent cleaning and surface safety performance was observed.

33 34 35 36 37 38 39 40

Nonionic from example 8 3.0 - 1.0 - 3.2 - - -

Nonionic from example 1 - 3.0 2.0 - - - 4.0 8.0

Nonionic from example 3 - - 2.0 3.2 - 3.2 4.0 -

C23E3 1.0 1.0 1.5 1.3 1.3 1.5 3.0 3.5

C24E21 2.0 2.0 2.5 1.9 1.9 2.0 5.0 6.0

NaPS 2.0 1.5 1.2 1.2 1.0 1.7 3.0 2.5

NaTS 1.2 3.0 2.2 2.0 2.0 1.5 4.0 5.0

MgSO4 0.20 0.9 0.30 0.50 1.3 2.0 1.0 3.0

Citrate 0.3 1.0 0.5 0.75 1.8 3.0 1.5 6.0

NaHCO3 0.06 0.1 - 0.1 - 0.2 - -

Na2HPO4 - - 0.1 - 0.3 - - -

Na2H2P2O7 - - - - - - 0.2 0.5 pH 8.0 7.5 7.0 7.25 8.0 7.4 7.5 7.2

Water and Minors q.s. to 100% EXAMPLE 41 Automatic dishwashing compositions:

Ingredients: Wei ht %

A B

Sodium Tripolyphosphate (STPP) 24.0 45.0 Sodium Carbonate 20.0 13.5 Hydrated 2. Or Silicate 15.0 13.5

Nonionic Surfactant¹ 3.0 3.0

C_i4 Amine Oxide 1.0 1.0

Polymer² 4.0 —

Protease (4% active) 0.83 0.83

Amylase (0.8% active) 0.5 0.5

Perborate Monohydrate (15.5% active AvO)³ 14.5 14.5

Cobalt Catalyst⁴ 0.008 —

Dibenzoyl Peroxide (18% active) 4.4 4.4

Water, Sodium Sulfate, Misc. Jalance Balance

' Nonionic surfactant according to Example 1.

Teφolymer selected from either 60% acrylic acid/20% maleic acid/20% ethyl acrylate, or 70% acrylic acid/10% maleic acid/20% ethyl acrylate.

³ The AvO level of the above formula is 2.2%.

⁴ Pentaamineacetatocobalt(III) nitrate prepared as described hereinbefore; may be replaced by MnTacN.

The following examples further illustrate phosphate built ADD compositions which contain a bleach/enzyme particle, but are not intended to be limiting thereof.

These compositions are suitable for use in the methods of the present invenetion. All percentages noted are by weight of the finished compositions, other than the perborate (monohydrate) component, which is listed as AvO. EXAMPLES 42-43 Ingredients: Weight %

42 43

STPP 30.0 32.0

Na₂CO₃ 30.5 20.5

2 R Silicate (SiO₂) 8.0 4.0

Catalyst¹ 0.008 0.004

Savinase™ 12T — 1.1

Protease D 0.9 —

Perborate (AvO) 5.0 0.7

Polymer² 4.0 —

Dibenzoyl Peroxide 0.2 0.15

Paraffin 0.5 0.5

Benzotriazole 0.10 0.3

Cj₄ Amine Oxide 0.5 0.5

Nonionic Surfactant³ 2.0 2.0

Sodium Sulfate, Moisture Rαla

¹ Pentaamineacetatocobalt(III) nitrate; may be replaced by MnTacN.

Polyacrylate or Acusol 480N or polyacrylate/polymethacrylate copolymers.

Nonionic surfactant according to Example 7.

In compositions of Examples 42 and 43, respectively, the catalyst and enzymes are introduced into the compositions as 200-2400 micron composite particles that are prepared by spray coating, fluidized bed granulation, marumarizing, prilling, or flaking/grinding operations. If desired, the protease and amylase enzymes may be separately formed into their respective catalyst/enzyme composite particles, for reasons of stability, and these separate compositions added to the compositions.

The following examples further illustrate ADD granular compositions with chlorine bleach suitable for use in the methods of this present invention. EXAMPLE 44-45

Ingredients: Wei ght %

44 45

STPP 25 31 Na₂CO₃ 23.0 15.0

2 R Silicate (SiO₂) 17.5 25.0

Hypochlorite 1.0 3.0

Polymer¹ 2.0

Dibenzoyl Peroxide 0.15

Paraffin 1.0 1.0

Cι₆ Amine Oxide 0.5 1.0

Nonionic Surfactant² 2.0 3.0

Sodium Sulfate, Moisture

¹ Polyacrylate or Acusol 480N or polyacrylate/polymethacrylate copolymers

³ Nonionic surfactant according to Example 8.

The following examples further illustrate ADD liquid-gel compositions suitable for use in the methods of this present invention.

EXAMPLES 46-47

Ingredients: Weight %

46 47

STPP 32.0 25.0

Na₂CO₃ 0.7 2.0

2 R Silicate (SiO₂) 0.3 1.0

Savinase™ 12T 2.0 1.0

Termamyl™ 1.4 0.5

Perborate (AvO) 3.5 —

Cι₄ Amine Oxide 0.8 0.8 Nonionic Surfactant 3.5 3.5

Sodium Sulfate, Moisture Balance

¹ Nonionic surfactant according to Example 3.

The following examples further illustrate ADD rinse aid compositions suitable for use in the methods of this present invention.

EXAMPLES 48-49 Ingredients: Weight %

48 49

Citric Acid 10.0 15.0

Ethanol 5.0 10.0

HEDP Acid¹ 1.0 0.7

Sodium Cumene Sulfonate 15.0 10.0

Polymer² — 1.0

Cι₄ Amine Oxide 2.0 0.5

Nonionic Surfactant³ 8.0 8.0

Nonionic Surfactant⁴ 6.0

Moisture Rals

¹ l-Hydroxyethylidene-l,l-diphoshonic acid

² Polyacrylate or Acusol 480N or polyacrylate/polymethacrylate copolymers

³ Nonionic surfactant according to Example 1.

⁴ Nonionic surfactant according to Example 5. The following examples further illustrate ADD tablet compositions suitable for use in the methods of this present invention.

EXAMPLES 54-55 Ingredients: Weight %

50 ϋ

STPP 48.0 30 Na₂CO₃ 15.0 25.0 2 R Silicate (SiO₂) 4.0 8.0

Catalyst¹ 0.008 0.004

Savinase™ 12T — 1.0

Termamyl™ 0.6 0.5

Perborate (AvO) 10.0 15.0

Polymer² 2.0 2.0

Dibenzoyl Peroxide 0.2 0.15

Paraffin 1.0 1.0

Benzotriazole 0.5 0.5

Cι₄ Amine Oxide 1.0 1.0

Nonionic Surfactant³ 3.0 3.0

Sodium Sulfate, Moisture R ils ¹ Pentaamineacetatocobalt(III) nitrate; may be replaced by MnTacN Polyacrylate or Acusol 480N or polyacrylate/polymethacrylate copolymers

³ Nonionic surfactant according to Example 2f.

Claims

WHAT IS CLAIMED IS:

1. A process for preparing an ether-capped poly(oxyalkylated) alcohol having the formula:

wherein, R is selected from the group consisting of linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from 1 to 30 carbon atoms; R¹ may be the same or different, and is independently selected from the group consisting of branched or linear C₂ to C₇ alkylene in any given molecule; x is a number from 1 to 30; and R is selected from the group consisting of: (i) a 4 to 8 membered substituted, or unsubstituted heterocyclic ring containing from 1 to 3 hetero atoms; and (ii) linear or branched, saturated or unsaturated, substituted or unsubstituted, cyclic or acyclic, aliphatic or aromatic hydrocarbon radicals having from 1 to 30 carbon atoms;

9 1 provided that when R is (ii) then either at least one of R is other than C₂ to C₃ alkylene or R has from 6 to 30 carbon atoms; comprising the steps of:

(a) providing a vinyl ether of the formula

R²OCH=CH₂ wherein R is as defined above;

(b) providing an alkoxylated alcohol of the formula

RO(R'O)_xH wherein R, R¹, and x, are as defined above;

(c) reacting said vinyl ether with said alkoxylated alcohol in the presence of a catalyst to form said ether-capped poly(oxy alkylated) alcohol.

2. The process as claimed in Claim 1 wherein R is a linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic hydrocarbon radical having from 1 to 20 carbon atoms.

3. The process as claimed in any one of Claims 1-2 wherein R is a hydrocarbon radical of the formula:

-C(CH₃)₂R³ wherein R is selected from the group consisting of linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from 1 to 30.

4. The process as claimed in any one of Claims 1-3 wherein R is a 7 to 13 membered substituted, or unsubstituted polycyclic ring.

5. The process as claimed in any one of Claims 1-3 wherein R is selected from the group consisting of linear or branched, aliphatic hydrocarbon radicals having from 7 to 1 1 carbon atoms; x is a number from 6 to 10; and R² is selected from the group consisting of a hydrocarbon radical of the formula:

— C(CH₃)₂R³ wherein R³ is selected from the group consisting of linear or branched, aliphatic radicals having from 2 to 5 carbon atoms.

6. The process as claimed in any one of Claims 1-2 wherein R > 2 i ^■s a 4 to 8 member substituted, or unsubstituted heterocyclic ring containing from 1 to 3 hetero atoms.

7. The process as claimed in any one of Claims 1-2 and 6 wherein said heterocycle is selected from the group consisting of:

wherein each R⁷ is independently selected from the group consisting of hydrogen, linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic hydrocarbon or alkoxy radical having from 1 to 10 carbon atoms, or R⁷ is a saturated or unsaturated, substituted or unsubstituted, alicyclic or aromatic hydrocarbon or alkoxy radical having, from 1 to 10 carbon atoms, which is fused to the heterocyclic ring; each A is independently selected from the group consisting of O, and N(R^s)_a, wherein R is independently selected from the group consisting of hydrogen, linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic hydrocarbon radical having from 1 to 10 carbon atoms, and a is either 0 or 1; z is an integer from 1 to 3.

8. The process as claimed in any one of Claims 1-2 and 6-7 wherein said heterocycle is selected from the group consisting of:

9. The process as claimed in any one of Claims 1-2 wherein R is a hydrocarbon of the formula:

— (CH₂)_y- X wherein, y is an integer from 0 to 7: and X, is a 4 to 8 membered substituted, or unsubstituted, partially unsaturated cyclic or aromatic hydrocarbon radical.

10. The process as claimed in any one of Claims 1-2 and 9 wherein R is selected from the group consisting of linear or branched, aliphatic hydrocarbon radicals having from 7 to 11 carbon atoms; x is a number from 6 to 10; and R² is selected from the group consisting of a hydrocarbon radical of the formula:

— (CH₂)_y-X wherein y is 0 and X, is a 5 or 6 membered substituted, or unsubstituted, saturated or unsaturated cyclic or aromatic hydrocarbon radical.

11. The process as claimed in any one of Claims 1-2 and 9 10 wherein y is 0 and X, is a 5 or 6 membered substituted, or unsubstituted, saturated or unsaturated cyclic or aromatic hydrocarbon radical.

12. The process as claimed in any one of Claims 1-2 and 9-1 1 wherein X is selected from the group consisting of:

wherein each R is independently selected from the group consisting of hydrogen, linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic hydrocarbon or alkoxy radical having from 1 to 10 carbon atoms, or R⁹ is a saturated or unsaturated, substituted or unsubstituted, alicyclic or aromatic hydrocarbon radical having, from 1 to 10 carbon atoms, which is fused to the ring; w is an integer from 1 to 3.

13. The process as claimed in any one of Claims 1-2 and 9-12 wherein X is selected from the group consisting of:

wherein R »9 i ^•s defined as above.

14. The process as claimed in any one of Claims 1-2 and 9-13 wherein X is selected from the group consisting of:

15. The process as claimed in any one of Claims 1-14 wherein said catalyst is selected from the group consisting of mineral acids and Lewis acids.

16. The process as claimed in any one of Claims 1-14 wherein said catalyst is selected from the group consisting of TiC_2, Ti(O^JPr)4, ZnCl₄, SnCl4, AICI3, BF3-OEt2_; poly(4-vinylpyridinium p-toluenesulfonate), DOWEX 50X8-50, H-Y Zeolite, REILLEX 425, pyridinium p-toluenesulfonate, AMBERLYST®15 p-toluenesulfonic acid, methanesulfonic acid and mixtures thereof.

17. The process as claimed in any one of Claims 1-16 wherein 0.1 mol % to 20.0 mol % of said catalyst is used in said step (c).

18. The process as claimed in any one of Claims 1-17 wherein said step of reacting of alcohol with alkoxylated alcohol is conducted in the presence of a solvent and wherein said solvent is selected from the group consisting of benzene, toluene, xylene, mesitylene, dichloromethane, tetrahydrofuran, diethylether, methyl tert- butylether, acetone, acetonitrile, and mixtures thereof.

19. The process as claimed in any one of Claims 1-18 wherein said step of reacting alcohol with alkoxylated alcohol is conducted as a temperature of from -20°C to 300°C.

20. The process as claimed in any one of Claims 1-17, and 19 wherein said step of reacting alcohol with alkoxylated alcohol is conducted in the absence of a solvent.

21. The process as claimed in any one of Claims 1-20 wherein said process further comprises step

(d) isolating the ether-capped poly(oxyalkylated) alcohol surfactant produced in said step (c) by striping the product of step (c) in the presence of a base.

22. The process as claimed in Claim 1 wherein said process further comprises (e) removal of color bodies and odors from the product of step (c).

23. The process as claimed in any one of Claims 1-22 wherein said ether-capped poly(oxyalkylated) alcohol surfactant produced in said step (c) is removed from the product of step (c) by centrifuging.

24. An ether-capped poly(oxyalkylated) alcohol surfactant produced by a process as claimed in any one of Claims 1-123.

25. A composition comprising an ether-capped poly(oxyalkylated) alcohol surfactant produced by a process as claimed in any one of Claims 1-23.