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Publication numberUS2456283 A
Publication typeGrant
Publication dateDec 14, 1948
Filing dateApr 30, 1945
Priority dateApr 30, 1945
Publication numberUS 2456283 A, US 2456283A, US-A-2456283, US2456283 A, US2456283A
InventorsGeorge D Jefferson
Original AssigneeAtlas Powder Co
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Textile wax compositions
US 2456283 A
Abstract  available in
Images(4)
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Claims  available in
Description  (OCR text may contain errors)

,, terials.

Patented Dec. 14, 1948 TEXTILE WAX COMPOSITIONS George D. Jefferson, Kennett Square, Pa., as-

slgnor to Atlas Powder Company, Wilmington, Del., a corporation of Delaware No Drawing. Application April 30, 1945,

Serial No. 591,237

The present invention relates to improvements in hydrocarbon wax compositions.

' An object of the invention is to prepare a hydrocarbon wax composition that is particularly useful as a textile sizing material.

Another object is to provide such wax compositions that, after thelrapplication, as for example as a textile size, are easily scourable in water.

A more specific object is to provide textile sizing compositions, certain of which are capable of application either in the form of solutions 'in hydrocarbon solvents or in the form of emulsions with water, said compositions being capable of ready removal from the textile materials by reason of their dispersibility in water.

The above and other objects will become more fully apparent in the course of the following description.

The invention will be described particularly with reference to its use in the textile art, but it will be understood that the composition has properties that are useful in other arts.

Hydrocarbon waxes represent a plentiful source of materials that possess physical properties of lubricity and ability to form a coating, that are desirable in the processing of textile ma- However, these waxes are soluble only in certain non-aqueous solvents as a result of which their usefulness in the textile field has been limited. Solutions of hydrocarbon waxes can be applied to textile materials from non-aqueous solvents, but they are particularly objectionable because of high solvent retention and the difiiculty in removing all traces of the wax when that becomes necessary. In particular, it is desirable in the processing of certain textile materials to apply a waxy coating to a yarn for the purpose of retaining twistand imparting lubricity during a knitting operation. At the conclusion of the knitting operation, the waxy coating must be removed to prepare the fabric for further operations, such as dyeing, and to render the fabric suitable for use. The hydrocarbon waxes themselves have not been considered to be useful as textile size materials because of the difficulties involved in the removal of the hydrocarbon wax from the fabric without injury thereto. Various attempts have been made to mix hydrocarbon waxes with different substances to render them more easily removable from a fabric. However, these earlier proposals have not been satisfactory either because of the characteristics of the compositions produced or because of the adverse effects of the compositions on the textile material or the machines used in handling it.

3 Claims. (Cl. 106--268) The present invention provides a hydrocarbon wax composition which has highly desirable coatterlals or on the machines used in handling them.

' polyoxyethylene ether ester of a straight-chain monobasic aliphatic acid having at least 12 car The compositions of the present invention comprise three ingredients; namely, the hydrocarbon wax, an emulsifier and a coupling or blending agent. The emulsifier has sufllcient hydrophylic properties to render the composition, which is otherwise of a predominantly hydrophobe material, readily scourable in water. The coupling or blending agent tends to make the hydrophobe hydrocarbon wax and the hydrophilic emulsifier compatible, assists in making the composition scourable, and, at the same time,.

contributes other desirable properties to the composition. By varying the proportions of the materials, compositions of different degrees of hardness, titer, etc. can be formulated for best results under particular conditions.

The hydrocarbon 'wax employed in the compositions of the present invention is preferably a paraffin wax, for example, white crude scale wax of 124/126 A. M. P., a refined wax of /137 A. M. P. or a blnd of paraffin wax with petrolatum or mineral 011. Other petroleum waxes, the fossil waxes or blended waxes such as'ceresin can be used. As will be understood, other types of waxes such as carnauba, beeswax, or Japan wax, can be blended with the hydrocarbon wax to alter the physical properties of the latter.

The emulsifier used in the wax composition of the invention is a water-dispersible to.soluble bon atoms and not more than one unsaturated carbon to carbon bond. As is well-known, the minimum number of oxyethylene groups in the water-dispersible to soluble esters of this class varies depending upon the chain length of the acid and the number of the acid groups present. The esters having the longer chain acids require more oxyethylene groups to make them waterdispersible than do the esters of the shorter chain acids. Similarly, esters with two or more acid groups present require more oxyethylene groups to make them water-dispersible than do the esters having only one acid group present. While groups is permissible.

an ester having oxyethyiene: groups present an amount in excess of the number required make the ester water-soluble may be employed.

the' preferred esters are those in which the ox?- ethylene groups are not present in great excess over the number required to renderthe ester water-soluble. A large excess of oxyethylene groups over the number required to render the ester soluble contributes nothing to the ultimate I composition and may render it too hydrophilic;

Examples of ether esters falling within this class are the vwater-dispersible to soluble polyethylene glycol'esters of the fatty acids. These esters can be prepared either by esterifying a polyglycol or by reacting the fatty acid with ethylene oxide. Of this type, the preferred emulsifiers are the polyethylene glycol monoesters of the fatty acids which contain a number 0! oxyethylene groups equal at least to the value where c is the number of carbon atoms in the acid. A particularly valuable member of this group is a polyglycol monostearate produced by the reaction of ethylene oxide and stearic acid in the proportion of 20 mols of ethylene oxide per mol of stearic acid. Another emulsifier of this group-is the polyglycol laurat-e with about 8 oxyethylene groups per mol of lauric acid. Further examples of the polyethylene glycol ester type are the polyglycol distearates which contain from 20 to 40 ethenoxy groups.

Another group of ether esters falling within this class are those in which the cxyethylene groups are coupled to the acid through polyhydric compounds, preferably those having at least 3 hydroxyi groups and from 3 to 6 carbon atoms, such as glucose or other sugar, hexitols, hexitans, hexides, glycerol, diglycerol, or the like. Specific examples of these emulsifiers are the products produced by adding an average of 20 ethenoxy groups to a sorbitan monoester of lauric or stearic acid.

A further type of emulsifier that can be used is prepared by first reacting a polyhydric composition such as a hexitol or sugar with ethylene oxide to form a polyhydroxy ethyl ether and then partially esterifying the ether with the selected acid. A specific example of such an emulsifier is a disterate of glucose polyoxyethylene ether in which the ether has approximately six oxyethylene groups per mol of glucose.

All of these emulsifiers contain a plurality of oxyethylene groups, other groups, and at least one ester group. Accordingly, the term polyoxyethylene ether ester" is used to include all oi I these variations. Mixtures of two or more emulsifiers of this class can be used. It should also be noted that commercial products of the types defined are actually mixtures due. to the facts that commercial fatty acids are usually mixtures of homologous acids, and also the process by which the polyoxyethylene ether esters are made give rise to a number of products rather than a single compound. In particular, reactions with ethylene oxide produce a series of compounds of diilerent polyoxyethylene chain lengths which are designated in trade and in the literature by a single name referring to. the average chain length. While the polyoxyethylene chains are generally uninterrupted, it will be apparent that the presence of other hydrophilic oxyalkylene For example, the ether esters can contain polyoxyalkylene chains comassasss posed of alternate oxyethylene and oxymethylene groups such as the compounds produced by reacting 1,3-dioxolane with the aliphatic acid or an ester thereof.

The coupling or blending agent used in the composition of the invention is selected from the on solution in hydrocarbon solvent, and on dispersion in water.

The aliphatic acid used as coupling agent serves several other useful functions in the composition, Among these other functions are the reduction of solvent pickup, or conversely more rapid release of solvent, which results in achieving a strong, firm coating within a short time after applica tion. In the coating the free acid also has the eifect of tempering the composition and reducing powdering. The coupling agent is selected with due regard to the physical characteristics of the hydrocarbon wax and the emulsifier so that the final product has the desired physical properties. As in the case oi the emulsifiers, the coupling agents include materials ranging from liquids to hard waxes so that by selecting different members of the series the characteristics of the compositions can be varied.

The proportions of the three ingredients may be varied over relatively wide ranges within which it is possible to obtain compositions with variations in hardness, titer, film strength, ease of dispersibility in water and other properties.- It is also possible to obtain a large number of compositions of different ingredients which have essentially the same properties. However, in the compositions of the present invention, the emulsifiers and coupling agent are each used in substantial proportions, the emulsifier being present in the wax composition in a proportion of at least 6% and the coupling agent being present in a proportion of at least 10%. The hydrocarbon wax may vary from 20 to 75%, th balance of 100% being made up of the emulsifier and coupling agent. The preferred compositions of the present invention contain at least 40% of the wax. Thus, for example, a preferred composition is one containing from 40 to 70% white crude scale wax 124/126 A. M. P., 10 to 40% stearic acid and 6 to 30% of a. polyglycol monostearate produced by the reaction of ethylene oxide .and stearic acid in the proportion of 20 mols of eth lene oxide per mol of stearic acid.

Examples positions was compatible in the molten condition,

although in some cases it was necessary that a small amount of water, on the order of 1% or less be present. Where the addition of this small amount of water was required, it was noted to t i have no adverseeffect on hydrocarbon solvent solubility or the other properties oi the composition. The compositions in the table were soluble to the extent of at least 50% in Stoddards solvent at a temperature of 60 C. and the compositions were insoluble or substantially less than 50% soluble in that solvent at room temperature. Solubility at elevated temperature is important since the preferred method of applying these As an example of the application to yarn of a composition or the present invention in the form of a solution of the composition in a hydrocarbon solvent, the following is given.

A 50% solution of the composition of Example 1 in Stoddard solvent at about 60 C. is prepared and the yarn is soaked therein for to 20 minutes. The yarn is then removed from the solution and placed in a centrifugal extractor to 'waxy sizes to yarns is to treat the yarns with a 10 remove excess solution. The soaking and exwarm solution which, oicourse, makes the solvent tracting operation should be performed to leave evaporate more readily-after the yarn leaves the about 8 to 10% of the composition on the yarn. bath. Insolubility at room temperature iacili- Following the extraction, the yarn'can be wound tates complete solvent release from the coating. immediately on spools and then twisted or used The compositions were also evaluated for disin other ways. During a twistin operation, the persibility in water by stirring 10 grams of the residual Stoddard solvent evaporates and the composition in 200 cc. of distilled water at 60 waxy coating servesto hold the twist in the yarn. C. The emulsions so prepared were allowed to Whether the yarn is twisted or not, the waxy stand overnight to determine their stability. All coating is advantageous because of the lubricity of the compositions in the table gave emulsions it imparts and the improvement in knitting and that remained stable by this test. handling properties resulting from its use. After Example Wax Percent oupling Agent Percent Emulsiiier Percent white crude scale 124/126 45 stearicacid .30 polygly'col monostearatc average 20 ethenoxy 26 A. M. P. groups per mol stearic acid.

50 so ..do

do palmitic acid ..do 76 ..do 20 myristic acid. 30 ..do 60 ...do... 20 ..do 60 stearic acid...

46 ..do 45 ..do

45 28 microcrystalline 30 20 white crude scale 124/126 50 A.M.P. 30 do Si -do The compositions are prepared as indicated above by mixing the ingredients together at a temperature suiflcient to melt them all. After cooling, the product is preferably comminuted or powdered for the convenience of users.

The compositions of the present invention'may be applied to yarn or other products which it is yarns such as yarns of viscose rayon, cuproammonium rayon and cellulose acetate. The compositions can be applied to yarn in skein or cake form or on 53 or twister bobbins.

position from the material. v

lose acetate knitted goods are completely scoured polyglycol distearate, average 20 ethenoxy groups perm v sorbitan trioieate polyglycol ether, 20 ethenoxy groups.

sorbitan monostearate poiyglycol ether, 20 ethonox groups.

pol g yool distearate, 40 ethenoxy groups sor itnntrioleate polyglycol ether, 20 othenoxy oups.

po yzlycol monostearate, 20 othenoxy groups distearate oi glucose polyoxycthylene other, 6

ethenoxy groups.

sorbitan monolaurate polyoxyethylene ether, 20

ethcnoxy groups.

sorbitan monostearate polyoxyethylone ether, 20

ethenoxy groups per mol.

8 8 888! i E3 53 88888588$23888f2858 Q the yarn is knitted, for example, the waxy composition can be removed either in a. separate operation or in the dye bath. In a combined scouring and dyeing operation in the case of knitted viscose it is recommended to use a boiling solution of the dyes, 6% soap, 2% pine oil, and 3% tetrasodium pyrophosphate based on weight of the goods. ,After 10 minutes of scouring and dyeing Glaubers salt is added in amounts up to 5%. The goods are then removed from the bath, rinsed, and finished for use. It is not necessary to use a boiling solution to scour the waxy com- For example, celluand dyed in a bath at a temperature of about 160 F. (71 C.)

The following is an example of the application of a composition of the invention to yarn by means of an aqueous emulsion. An emulsion containing 10 to 20% of the composition of Example 1 is prepared by mixing the composition and water at about 60 C. The yarn is then soaked in the emulsion, extracted in a centrifuge,

and dried. The yarn then carries the waxy coating and can be usedln the same way as the yarn treated with hydrocarbon solution described above. An advantage of the composition used resides inthe fact that even distribution is obtained when yarn in cake form is soaked in the emulsion. ,A number of emulsiilable compositions that have been suggested as yarn sizes give unsatisfactory results on application to yarn in this form due to a wicking eifect which concentrates the size at the outside layer of the cake.

In the foregoing examples of yarn sizing, the treating baths. hydrocarbon solvent solutions or 40 to 70% paramn scale wax, 6 to 30% of a polyaqueous emulsions can be used repeatedly with necessary replacement or the-amount absorbed by the yarn. Likewise the eiiluent from the centrifugal extractor can be returned to the bath and reused.

The invention has been described as applied to use as a textile size since it is in that field that it has the greatest usefulness at the present time. The properties of the compositions of the invention, however. suggest their use for other purposes where it is advantageous to deposit a waterdispersible waxy coating on a surface.

It will be understood that the compositions oi the invention can be used in conjunction with other substances. Various substances, such as .coloring agents or agents designed to accomplish some other effect on the yarn or other material to be treated, can be added to the compositions or to their solutions or emulsions provided, of course. that they do not adversely affect the composition.

What is claimed is:

ethylene glycol monostearate produced 'by the reaction of ethylene oxide and stearic acid in the proportion of about 20 mols ethylene oxide per mol of stearic acid, and 10 to 40% stearic acid, to

make a total of 100% of said mixture.

3. A solid composition consisting essentially of about paraflln scale wax of 124/126 A. M. P., about 30% stearic acid, and about 25% of a polyethylene glycol monostearate produced by the reaction oi ethylene oxide and stearic acid in the proportion of 20 mols ethylene oxide per mol of stearic acid.

GEORGE D. JEFFERBON.

REFERENCES CITED The following references are of record in the file of this patent:

UNITED s'm'ms PA'I'ENTS

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US1826900 *Oct 24, 1928Oct 13, 1931Firm Of Th Goldschmidt A GProcess of producing emulsions
US2127586 *Dec 5, 1933Aug 23, 1938Celanese CorpPile fabric and method of making the same
US2144642 *Aug 2, 1933Jan 24, 1939DavisComposition for and method of preventing silver from tarnishing
US2328431 *May 16, 1939Aug 31, 1943Gen Aniline & Film CorpProcess for rendering textile materials water repellent
US2347679 *Oct 18, 1941May 2, 1944Komel CorpWax emulsion
US2374931 *Mar 26, 1942May 1, 1945Atlas Powder CoWax composition
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US2598666 *Jun 30, 1948Jun 3, 1952Johnson & Son Inc S CWax composition
US2669524 *Sep 8, 1950Feb 16, 1954Johnson & Son Inc S CWater-repelling composition
US2670303 *Sep 8, 1950Feb 23, 1954Johnson & Son Inc S CWater-repelling composition
US2690426 *Mar 7, 1950Sep 28, 1954Atlas Powder CoLubricating compositions
US2690427 *Dec 14, 1949Sep 28, 1954American Viscose CorpTextile composition
US2696444 *Aug 30, 1949Dec 7, 1954Monsanto ChemicalsModified silica aquasol and textile fibers treated therewith
US2702796 *May 31, 1950Feb 22, 1955Atlas Powder CoTextile size comprising a partially neutralized polymethacrylic acid
US2755189 *Jun 24, 1954Jul 17, 1956American Machinery CorpCoating process for fruits and vegetables
US2783161 *Feb 1, 1952Feb 26, 1957Moore & MungerWax compositions
US2806804 *Dec 29, 1952Sep 17, 1957Drew & Co Inc E FMethod of treating wool
US2820724 *Dec 23, 1953Jan 21, 1958Du PontTextile treatment
US3000753 *Feb 21, 1957Sep 19, 1961Rockland Louis BEmulsified wax compositions
US3335209 *May 18, 1966Aug 8, 1967Monsanto CoMethod of treating polyester filaments
US3427192 *May 20, 1964Feb 11, 1969Deering Milliken Res CorpTextile sizing composition
US3457340 *Mar 25, 1966Jul 22, 1969Du PontProcess for uniform application of finish to polyester yarns
US3470095 *Feb 1, 1966Sep 30, 1969American Cyanamid CoAqueous textile treating emulsion
US5539035 *Oct 12, 1994Jul 23, 1996The Mead CorporationRecyclable wax-coated containers
WO1994018272A1 *Jan 10, 1994Aug 18, 1994Mead CorpRecyclable wax-coated containers
Classifications
U.S. Classification106/268, 252/8.83, 106/271
International ClassificationD06M13/02, C08K5/103, C08K5/09
Cooperative ClassificationC08K5/09, C08K5/103, D06M13/02
European ClassificationC08K5/103, C08K5/09, D06M13/02