Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.


  1. Advanced Patent Search
Publication numberUS3383320 A
Publication typeGrant
Publication dateMay 14, 1968
Filing dateAug 10, 1965
Priority dateAug 10, 1965
Publication numberUS 3383320 A, US 3383320A, US-A-3383320, US3383320 A, US3383320A
InventorsBell Jr Gordon W
Original AssigneeAvisun Corp
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Detergent bar
US 3383320 A
Abstract  available in
Previous page
Next page
Claims  available in
Description  (OCR text may contain errors)

United States Patent 3,383,320 DETERGENT BAR Gordon W. Bell, Jr., Wilmington, DeL, assignor to Avisun Corporation, Philadelphia, Pa., a corporation of Delaware N0 Drawing. Filed Aug. 10, 1965, Ser. No. 478,761 8 Claims. (Cl. 252132) This invention relates to a novel detergent bar, and more particularly to a detergent bar composed of a detergent held in a matrix of a sintered thermoplastic resrn.

It is an object of this invention to produce a detergent bar which will retain its original dimensions until substantially all of the detergent has been extracted therefrom.

It is a further object of this invention to provide a detergent bar which, in use, exerts a mildly abrasive action.

In accordance with the invention, these objects are attained by intimately mixing with the detergent a powder of a thermoplastic resin, heating the mixture to a temperature at which the powder will sinter, and then forming the mixture into a bar of the desired size and shape. It is essential to the invention that the mixture contain from about to about of the powder, since at lower concentrations of powder the bar will not retain it orignal dimensions during use, and at higher concentrations of powder a considerable amount of detergent cannot be leached from the bar during use, and is thus wasted.

The thermoplastic resin component of my novel detergent bar may be any thermoplastic resin having a melting point low enough that the detergent component of the composition will not decompose during the formation of the bar. Such resins include polyethylene, polypropylene, ethylene-propylene crystalline block copolymers, polystyrene, acrylic resins, acrylic copolymers, nylon, vinyl polymers and copolymers such as polyvinyl chloride and polyvinyl butyral, cellulosic plastics such as cellulose acetate and cellulose butyrate, and other thermoplastic polymers of similar nature.

The detergent component of the bar may be any watersoluble material having surface-active properties such as the sodium and potassium soaps of fatty acids. It is noteworthy that the potassium soaps may be utilized in my bar, since heretofore it has not been practicable to use such soaps in bar form due to their very soft consistency. Synthetic detergents may also be used. Examples of anionic detergents useful for my purpose include the alkali metal, ammonium, and alkaline earth metal salts of long chain alkyl aryl sulfonates, such as the sodium salt of dodecyl benzene sulfonate; N-lon'g chain acyl N-alkyl taurates, such as sodium oleoyl methyl taurate; long chain alkyl oxyethylene sulfates, such as sodium laurylpolyoxyethylene sulfates; long chain alkyl aryl oxyethylene sulfates, such as ammonium nonylphenol polyoxyethylene sulfate; long chain alkyl sulfates, such as potassium lauryl stearate; and long chain alkyl isothionates such as sodium lauryl isothionate, and mixtures thereof.

The detergent component may also consist of a nonionic surfactant, such as the condensation product of an epoxide such as ethylene oxide with a fatty acid, an alkyl phenol, an alkyl mercaptan, a fatty alcohol, or a fatty amide, provided only that sufiicient epoxide is incorporated into the molecule to render it water soluble.

Cationic surfactants such as long chain quaternary ammonium salts or salts of higher alkyl amines, for example, cetyltriethylammonium chloride or diethy1methyl-(-2- oleamidoethyl) ammonium methyl sulfate can also be used as the detergent component.

It will be understood that builders such as sodium sulfate or sodium tripolyphosphate may also form a part of the detergent component.

3,383,320 Patented May 14, 1968 In order that those skilled in the art may better comprehend the nature of my invention and the method of carrying it out, the following examples are given.

Example 1 Five parts by weight of soap and one part by weight of a mixture of monoand di-fatty acid glycerides were melted. About one-half part by weight of polypropylene powder was gradually stirred into the melt, which was heated to 200 C. The resulting lump of molten polypropylene was removed, then placed in a mold and solidified. The bar retained its original dimensions after seven handwashings.

Examples 2 through 9 Various amounts of a commercial detergent powder recommended for use in cleaning laboratory glassware were mixed with various amounts of a thermoplastic resin. The mixtures were then heated on a hot plate until a sticky uniform mass was obtained. The temperature of the mass was about 200 C. in the examples in which polypropylene was used, and about 150 C. when low density polyethylene was used. This was then placed in a textured mold and cooled to yield a solid plate about oneeighth-inch thick in Examples 2 through 7 and one-inch thick in Examples 8 and 9. One-inch squares were cut from each plate and extracted with warm water until a negligible amount of detergent was detected in the wash water. The squares were then weighed and observed for physical appearance. Results of these tests are given in the following table:

TABLE 1 Percent Percent Appearance Ex. N0. Resin (by wt.) Detergent of Square Resin Extracted 50 30 Firm.

10 97 Soft and crumbly.

20 96 Firm.

P P Crystalline polypropylene. PPE Propylene-ethylene crystalline block copolymer. PE Polyethylene.

during use. However, at 20 and 30% concentration, 90%- and over of the original detergent content was usable, and the squares retained their original dimensions.

While in the foregoing examples the powder mixture was sintered prior to being placed in the mold, it should be obvious to those skilled in the art that the powder mixture may be placed in a mold and heated therein to the sintering temperatue.

The invention claimed is:

1. As a new composition of matter, a detergent bar consisting of a solid water soluble detergent selected from the group consisting of soaps, anionic, nonionic and cationic detergents held in a solid matrix of a sintered thermoplastic resin, wherein the sintered resin constitutes from about 15% to about 35% of the Weight of the bar.

2. The composition of claim 1 wherein the resin is polypropylene.

3. The composition of claim 1 wherein the resin is a crystalline propylene-ethylene copolymer.

4. The composition of claim 1 wherein the resin is polyethylene.

5. Method of forming a detergent bar which comprises intimately mixing a solid water soluble selected from the group consisting of soaps, anionic, nonionic and cationic detergents with a powdered thermoplastic resin, wherein the resin constitutes from about 15% to about 35% of the Weight of the mixture, heating the mixture to the sintering temperature of the resin, and cooling to ambient temperature.

6. The process of claim 5 wherein the resin is polypropylene.

7. The process of claim 5 wherein the resin is a crystalline propylene-ethylene copolymer.

8. The process of claim 5 wherein the resin is polyethylene.

References Cited UNITED STATES PATENTS Chaplin 252-430 Alderson 26023 Haward et a1. 26023 Leeds 167-92 Ginn 252-89 Blaustein 16792 Siegele 252132 LEON D. ROSDOL, Primary Examiner.

W. E. SCHULTZ, Assistant Examiner.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US1362393 *Jun 7, 1915Dec 14, 1920Chaplin Edwin DSoap or cleaning compound
US2455910 *Feb 20, 1945Dec 14, 1948Du PontMethod for curing ethylene polymers
US2994675 *Oct 26, 1956Aug 1, 1961Shell Oil CoPolyamine stabilizers for polymerized alpha-olefins
US3055297 *Jan 14, 1957Sep 25, 1962Johnson & Son Inc S CMicroporous synthetic resin material
US3060124 *Dec 28, 1956Oct 23, 1962Monsanto ChemicalsLiquid detergent gel compositions having stability against separation
US3196079 *Oct 5, 1959Jul 20, 1965Phillips Petroleum CoCosmetic powder compositions containing polyethylene
US3284364 *Jan 25, 1963Nov 8, 1966American Cyanamid CoSoil anti-redeposition agents
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3494869 *Jul 11, 1966Feb 10, 1970Lever Brothers LtdSuperfatted soap bars and process for their preparation
US3903410 *Apr 2, 1973Sep 2, 1975Harold S AkrongoldWashing polymers
US4735746 *Mar 23, 1987Apr 5, 1988Texaco Inc.Long lasting detergent bar containing a polyamide or polyester polymer
US5109061 *Mar 2, 1990Apr 28, 1992Texaco Chemical CompanySurfactants containing a polyurethane or polyurea polymer
US5139706 *Feb 12, 1991Aug 18, 1992Texaco Chemical CompanyFatty amides prepared by reacting dicarboxylic acids, polyoxyalkylene amine bottoms products and fatty acids or esters thereof
US5527488 *Mar 10, 1995Jun 18, 1996Amway CorporationHigh viscosity anhydrous makeup remover gel
US7012057 *Oct 28, 2002Mar 14, 2006Unilever Home & Personal Care Usa, Division Of Conopco, Inc.Detergent bars comprising radiation curable resins
US20050014666 *Oct 28, 2002Jan 20, 2005Bir KapoorDetergent bars
U.S. Classification510/143, 510/146, 510/475, 510/440
International ClassificationC11D17/04
Cooperative ClassificationC11D17/048, C11D17/006
European ClassificationC11D17/04D, C11D17/00H6