US3355413A - Polyester fibers resistant to resoiling during laundering - Google Patents
Polyester fibers resistant to resoiling during laundering Download PDFInfo
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- US3355413A US3355413A US586671A US58667166A US3355413A US 3355413 A US3355413 A US 3355413A US 586671 A US586671 A US 586671A US 58667166 A US58667166 A US 58667166A US 3355413 A US3355413 A US 3355413A
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- polyester
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- ethylene glycol
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- soil
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
- D01F6/92—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
Definitions
- Polyester fibers having improved resistance to resoiling during laundering may be prepared by dispersing a fatty acid ester of a poly(ethylene glycol) in said polyester prior to spinning and then spinning said fibers from said polyester.
- This invention concerns a method for improving polyester fibers by treating the polyester with polyethers before melt spinning.
- Laundering consists essentially of removing soil from the fabric and keeping the soil in suspension so that it can be rinsed away.
- soap or a synthetic detergent is used to wet thfabric and emulsify or disperse the soil. Soap is fairly effective in preventing the soil from redepositing on the fabrics in the laundry solution. However, most synthetic detergents do not performthis important function. Therefore, many laundry detergent formations contain a detergent additive which prevents the redeposition of the, soil on the fabric.
- a common and widely used detergent additive. is carboxymethylcellulose which is very effective in preventing soil from redepositing on cottonfabrics, but which has no effect in preventing re deposition of soil on most synthetic fabrics during laundering.
- the above objects are attained by treating polyesters and fabrics in such a way as to disperse a polyether in the polyester before spinning and to then melt spin the polyester having the polyether dispersed therein into a fiber.
- the polyether and polyester can be mixed together by dry mixing in appropriate mixing equipment, such as a Banbury mixer, a sigma blade mixer, or in a revolving drum.
- the polyester can be formed into pellets, rods, powder, etc., and sprayed with liquid polyether before melt spinning.
- the polyether can be dissolved in a volatile solvent for the polyether which is a nonsolvent for the polyester.
- the polyester resin is then slurried in the polyether solvent solution, and the excess solution drained off.
- the solvent remaining on the polyester is evaporated and the coated polyester resin dried by heat and/or reduced pressure.
- Suitable solvents for polyether are water; alcohols, such as methanol, ethanol, and the-propanols; ketones, such as acetone and ethyl methyl ketone; esters, such as ethyl acetate and methyl acetate; chlorinated hydrocarbons, such as dichloromethane and dichloroethane; and aliphatic and aromatic hydrocarbons, such as benzene, toluene, hexane, etc.
- the polyether and the polyester can be mixed together on a hot roll 'such as is commonly used in. mixing plasticizers with thermo-plastic resins.
- a hot roll ' such as is commonly used in. mixing plasticizers with thermo-plastic resins.
- this method of mixing it is sometimes advantageous to mix a relatively high concentration of the polyether (5-30 percent) into a low molecular weight polyester.
- This mixture commonly called a masterbatch, is then mixed with the unmodified high molecular weight polyester to give the desired amount of polyether in the final mixture.
- the masterbatch technique is only one of the known methods which may be used to melt. mix the polyether and polyester in an extruder' such as is commonly used in mixing plasticizers with thermoplastic resins.
- polyesters are treated with certain polyethers under controlled conditions, the polyesters are considerably less susceptible .to discoloration caused by the absorption or adsorption ofsoil during laundering. v
- One object of this invention is to provide a method for treating polyester fibers to make them less susceptible to redeposition of soil during laundering. Another object is to provide polyester fibers and fabrics which are resistant tosoil redeposition duringlaundering. Another The above methodsof adding the polyether .to the polyester are illustrative of the many methods known to the art and are not intended to limit the practice of my invention. 7
- the polyethers which are useful in carrying out my having a molecular weight of at least 2,000 may use poly(ethylene glycols) such as those commercially sold by Union'LCarbide Company under the trade designations. Carbowax. 2,000, Carbowax 4,000, Carbo'w'ax '20M',Polyox'WSR 35, Polyox WSR-205, and Polyox 'WSR-30l. If the poly(ethylene glycol) has a molecular weight less than 2,000, the fatty acid ester derived therefrom will be a smaller molecule which tends to, come off during the wash cycle, thereby making for a less permanent treatment.
- decanoic lauric, 4-ehlorolauric, tridecanoie; myristic, pentadecanoic, 4-ethyl-S-chloropentadecanoic, arachidic, heneicosanoic, behenic, etc., acids.
- Fatty acids having less than carbon atoms do not produce the desired results, while those having more than 22 carbon atoms ofler no additional advantages.
- the amount of polyether required to produce the desired antisoil redeposition result is from about 0.25 to about 5 percent by weight, based on the weight-of the polyester. Fibers containing less than about 0.25 percent of the p'olye'ther discolor under normal laundenng conditions nearly as badly as the unmodified fibers. Increasing the concentration of the polyetlier above about 5 percent otters nofadditional advantages.
- Example 1 45 grams of poly(e thylene glycol) disteai ate prepared from a polyethylene glycol (Carbowax 4,000) andste'an'c acid, were dissolved in 350 milliliters of tolueneJIhe solution was added with stirring to 2,200 grams of pulverized polyester poly(1,4 cyclohexylenedirnethylene terepht-halate) of inherent viscosity of 0.82. The mixtiire was then dried at 60 C. and of mercury for three hours and melt spun into fibers which contained 2 percent by weight of the polyether additive. After drafting and heat setting, the yarn was knittedintoa sock.
- poly(e thylene glycol) disteai ate prepared from a polyethylene glycol (Carbowax 4,000) andste'an'c acid
- a samplept thesock was subjectedto a washing in the pres ence of heavily solid cotton. After three washings. the sample was not discolored.
- a control sample of .po1y(-l,4- cyclohexy-lenedirnethylene terephthalate) with :no poly ethylene glycol) distearate was dark gray in color after similar washings.
- Example 2 The procedure of Example 1 was followed with the exception that .poly(l,4-cyelohexylenedimethylene' te'rephthalate) was replaced with .poly(etliylene tere'phthal ate). Equally good results were 7 obtained after three washings when poly (etliylene glycol) distearate was added to the polyester. The sample containing no polyfet-hylene glycol) 'di's-teai'ate was discolored after three washings.
- Example 3 Polyeth lene glycol) disieaia'te prepared in Example 1 was injected into a molten stream or poly(l;$ cyclohexylenedimethylerle teieph'tnalaie) and V agitated therewith while molten. The feed rates were adjusted so that 2 percent by weight "of the poly(ethylene' glycol) distea'rate was present in the final polymer which had an inherent viscosity of 0.79. The final polymer was melt span in'to continrrocs filament which was drafted; heat set, and "converted into sane staple. The staple was then con verted into staple yarn and woven into fabric on a loom.
- Example 1 indicates that untreated poly( 1,4 cyclohexylenedimethylene tere'phtbalate.) becomes discolored under similar laundering conditions.
- Example 4 A polyester po ycl3teyclohexyr neeinrefliylene terephthalaten was pulverized and dividedinto three equal portions. one percent by weight of poly(ethylene glycol) ti'actate was "added to another portion of the polyester. Both of the polyt'eth lene glycol) 'e's'teis 'we're pre ared from a "polywiliylene glycol) with a noleenlar weight or 4,000 and the corresponding acid. The two sam les of pol ester 'co'ntainin'gfthe additive as well as "the untreat d sam le were spun into fibers. The fibers were drafted, heat set, and woven into socks as described in Example 1. The socks were all laundered the presence of heavily soiled cotton. The results of the laundering test-areshowa in Table I.
- the test consisted (ii is se arate aundering eyelesgsoned cottonfabrics were addeda't the beginning of each cycle. The ratingswere based on a l to 5 scale with the 1 rating b'eing b'est appearance, The first number in the column represents the rating received after the eighth cyc e.
- Example 6 A polyesterlpolytethylene terephthalateag was pulverized and divided into 6 equal portions. Gneportiori was used as a control. An additive was added to each of the other portions. The -6 samples were converted -soeks as in Example '1.
- Example 7 A polyester [poly(l,4 cyclohexylenedimethylene terephthalate)] was pulverized and divided into eight equal parts. An additive (1% based on the weight of the polyester) was added to each part, and the polyesters were converted into socks as in Example 1.
- the antisoiling additives and the laundering characteristics of the socks are shown in Table IV.
- Example 8 A polyester [poly(1,4-cyclohexylenedimethylene terephthalate)] was pulverized and divided into four equal parts. Poly(ethylene glycol) distearate was added to each portion, and the polyesters were converted into socks as in Example 1.
- this invention provides an especially advantageously new and useful polyester fiber having dispersed therein from about 0.25 to about 5 percent by weight, based on the weight of said polyester fiber, of a fatty acid ester of a poly(ethylene glycol), said fatty acid having 10 to 22 carbon atoms and said poly(ethylene glycol) having a molecular weight of at least 2,000.
- this invention provides an especially advantageous new and useful process for treating polyesters, said process comprising dispersing therein from about 0.25 to about 5 percent by weight, based on the weight of said polyester, of a fatty acid ester of a poly(ethylene glycol), said fatty acid having 10 to 22 carbon atoms and said poly(ethylene glycol) having a molecular weight of at least 2,000.
- this invention provides an especially advantageous new and useful process for preparing a soil resistant polyester fiber, said process comprising (a) mixing a polyester powder with from about 0.25 to about 5 percent by weight, based on the weight of said polyester, of a fatty acid ester of a poly(ethylene glycol), said fatty acid having 10 to 22 carbon atoms and said poly(ethylene glycol) having a molecular weight of at least 2,000, and (b) melt spinning said soil resistant polyester fiber therefrom.
- a process for preparing a soil resistant polyester fiber comprising (a) mixing a polyester powder with from about 0.25 to about 5 percent by weight, based on the weight of said polyester, of a fatty acid ester of a poly(ethylene glycol), said fatty acid having 10 to 22 carbon atoms, said poly(ethylene glycol) having a molecular weight of at least 2,000 and said polyester being prepared from at least one diol and at least one dibasic acid, (b) melt spinning said soil resistant polyester fiber therefrom.
- a soil resistant polyester fiber prepared by a process as defined in claim 1.
Description
United States Patent ABSTRACT OF THE DISCLOSURE Polyester fibers having improved resistance to resoiling during laundering may be prepared by dispersing a fatty acid ester of a poly(ethylene glycol) in said polyester prior to spinning and then spinning said fibers from said polyester.
This application is a continuation-in-part of Kiefer U.S. Serial No. 273,284, filed Apr. 16, 1963, now abandoned.
This invention concerns a method for improving polyester fibers by treating the polyester with polyethers before melt spinning.
Laundering consists essentially of removing soil from the fabric and keeping the soil in suspension so that it can be rinsed away. Normally, soap or a synthetic detergent is used to wet thfabric and emulsify or disperse the soil. Soap is fairly effective in preventing the soil from redepositing on the fabrics in the laundry solution. However, most synthetic detergents do not performthis important function. Therefore, many laundry detergent formations contain a detergent additive which prevents the redeposition of the, soil on the fabric. A common and widely used detergent additive. is carboxymethylcellulose which is very effective in preventing soil from redepositing on cottonfabrics, but which has no effect in preventing re deposition of soil on most synthetic fabrics during laundering. Consequentially, white goods of synthetic fabrics often develop a discoloration when laundered with other fabrics carrying a relatively heavy soil load,- since the soil is absorbed from the laundry solution by synthetic fabrics. This is particularly true in the case of polyesters which often have a gray appearance due to 3,355,413 Patented Nov. 28, 1967 object is to provide polyester fibers and fabrics which are resistant to soil redeposition even after dry cleaning.
The above objects are attained by treating polyesters and fabrics in such a way as to disperse a polyether in the polyester before spinning and to then melt spin the polyester having the polyether dispersed therein into a fiber.
Various methods may be employed for incorporating the polyether into the polyester material. For instance, the polyether and polyester can be mixed together by dry mixing in appropriate mixing equipment, such as a Banbury mixer, a sigma blade mixer, or in a revolving drum. The polyester can be formed into pellets, rods, powder, etc., and sprayed with liquid polyether before melt spinning.
The polyether can be dissolved in a volatile solvent for the polyether which is a nonsolvent for the polyester. The polyester resin is then slurried in the polyether solvent solution, and the excess solution drained off. The solvent remaining on the polyester is evaporated and the coated polyester resin dried by heat and/or reduced pressure. Suitable solvents for polyether are water; alcohols, such as methanol, ethanol, and the-propanols; ketones, such as acetone and ethyl methyl ketone; esters, such as ethyl acetate and methyl acetate; chlorinated hydrocarbons, such as dichloromethane and dichloroethane; and aliphatic and aromatic hydrocarbons, such as benzene, toluene, hexane, etc.
The polyether and the polyester can be mixed together on a hot roll 'such as is commonly used in. mixing plasticizers with thermo-plastic resins. When this method of mixing is used, it is sometimes advantageous to mix a relatively high concentration of the polyether (5-30 percent) into a low molecular weight polyester. This mixture, commonly called a masterbatch, is then mixed with the unmodified high molecular weight polyester to give the desired amount of polyether in the final mixture. The masterbatch technique is only one of the known methods which may be used to melt. mix the polyether and polyester in an extruder' such as is commonly used in mixing plasticizers with thermoplastic resins.
the accumulation of soil. Attempts have been made to 1 are, any of the condensation polymers prepared from overcome soil redeposition in the launderin'g'of polyesters, but the conventionally used treatments 'do not absorb-the optical 'brighteners present in most laundry detergent formulations and are not permanent even under ordinary laundering conditions. These conventional treatments process arefatty acidLesters of poly(ethylene glycols) often lose their elfectiveness after less than 30 cycles in an automatic washing machine. Also, the suggested treatments are not permanent to dry cleaning and are therefore useful only in fabrics which are never exposed toia dry cleaning bath.
I have now found that when polyesters are treated with certain polyethers under controlled conditions, the polyesters are considerably less susceptible .to discoloration caused by the absorption or adsorption ofsoil during laundering. v
One object of this invention is to provide a method for treating polyester fibers to make them less susceptible to redeposition of soil during laundering. Another object is to provide polyester fibers and fabrics which are resistant tosoil redeposition duringlaundering. Another The above methodsof adding the polyether .to the polyester are illustrative of the many methods known to the art and are not intended to limit the practice of my invention. 7
The polyesters with whichmy invention is concerned diols and dibasicv acids, or their derivatives. Particularly important are poly(ethylene terephthalate) and poly(l,4- cyclohexylenedimethylene terephthalate).
The polyethers which are useful in carrying out my havinga molecular weight of at least 2,000. For instance, I may use poly(ethylene glycols) such as those commercially sold by Union'LCarbide Company under the trade designations. Carbowax. 2,000, Carbowax 4,000, Carbo'w'ax '20M',Polyox'WSR 35, Polyox WSR-205, and Polyox 'WSR-30l. If the poly(ethylene glycol) has a molecular weight less than 2,000, the fatty acid ester derived therefrom will be a smaller molecule which tends to, come off during the wash cycle, thereby making for a less permanent treatment.
theseacids would include capric, 'S-methylcapric, un-
decanoic, lauric, 4-ehlorolauric, tridecanoie; myristic, pentadecanoic, 4-ethyl-S-chloropentadecanoic, arachidic, heneicosanoic, behenic, etc., acids. Fatty acids having less than carbon atoms do not produce the desired results, while those having more than 22 carbon atoms ofler no additional advantages.
The amount of polyether required to produce the desired antisoil redeposition result is from about 0.25 to about 5 percent by weight, based on the weight-of the polyester. Fibers containing less than about 0.25 percent of the p'olye'ther discolor under normal laundenng conditions nearly as badly as the unmodified fibers. Increasing the concentration of the polyetlier above about 5 percent otters nofadditional advantages.
The following examples are intended to illustrate my invention so that it may be easily understood but not to limit it in any way.
Example 1 45 grams of poly(e thylene glycol) disteai ate prepared from a polyethylene glycol (Carbowax 4,000) andste'an'c acid, were dissolved in 350 milliliters of tolueneJIhe solution was added with stirring to 2,200 grams of pulverized polyester poly(1,4 cyclohexylenedirnethylene terepht-halate) of inherent viscosity of 0.82. The mixtiire was then dried at 60 C. and of mercury for three hours and melt spun into fibers which contained 2 percent by weight of the polyether additive. After drafting and heat setting, the yarn was knittedintoa sock. A samplept thesock was subjectedto a washing in the pres ence of heavily solid cotton. After three washings. the sample was not discolored. A control sample of .po1y(-l,4- cyclohexy-lenedirnethylene terephthalate) with :no poly ethylene glycol) distearate was dark gray in color after similar washings.
Example 2 The procedure of Example 1 was followed with the exception that .poly(l,4-cyelohexylenedimethylene' te'rephthalate) was replaced with .poly(etliylene tere'phthal ate). Equally good results were 7 obtained after three washings when poly (etliylene glycol) distearate was added to the polyester. The sample containing no polyfet-hylene glycol) 'di's-teai'ate was discolored after three washings.
Example 3 Polyeth lene glycol) disieaia'te prepared in Example 1 was injected into a molten stream or poly(l;$ cyclohexylenedimethylerle teieph'tnalaie) and V agitated therewith while molten. The feed rates were adjusted so that 2 percent by weight "of the poly(ethylene' glycol) distea'rate was present in the final polymer which had an inherent viscosity of 0.79. The final polymer was melt span in'to continrrocs filament which was drafted; heat set, and "converted into sane staple. The staple was then con verted into staple yarn and woven into fabric on a loom. The material so prepared did not discolor after repeated washings in a home washer and dryer in the presence of heavily soiled cotton. Example 1 indicates that untreated poly( 1,4 cyclohexylenedimethylene tere'phtbalate.) becomes discolored under similar laundering conditions.
Example 4 A polyester po ycl3teyclohexyr neeinrefliylene terephthalaten was pulverized and dividedinto three equal portions. one percent by weight of poly(ethylene glycol) ti'actate was "added to another portion of the polyester. Both of the polyt'eth lene glycol) 'e's'teis 'we're pre ared from a "polywiliylene glycol) with a noleenlar weight or 4,000 and the corresponding acid. The two sam les of pol ester 'co'ntainin'gfthe additive as well as "the untreat d sam le were spun into fibers. The fibers were drafted, heat set, and woven into socks as described in Example 1. The socks were all laundered the presence of heavily soiled cotton. The results of the laundering test-areshowa in Table I.
TABLE I Polymer Composition Additive Lal i ndier ing Poly(1,-cyclohexylenedimethylls ione 5-H- ene terephthalate).
Do 1% poly(ethylene 2-1 glycol) distearate. Do 1%1'iolflethylene 3-4 glycol) diacet-ate.
The test consisted (ii is se arate aundering eyelesgsoned cottonfabrics were addeda't the beginning of each cycle. The ratingswere based on a l to 5 scale with the 1 rating b'eing b'est appearance, The first number in the column represents the rating received after the eighth cyc e.
The results of these tests indicate that fibers containing poly(ethylene glycol) diacetate are somewhat superior to fibers without an additive, but not nearly as good as fibers containing poly(ethylene glycol) distearate.
V Eidfilpl A polyester [polyti 4-cyclohexyleneiiimethylene ter- 7 ephthala ten was pulverized and divided into four equal portions and mixed with the amount and composition of the additives shown in Table II. The four samples were spun into fibers as in Example 1 which were drafted, hea t set, and woven into socks as described in Example I. 'The socks were laundered in the presence of heavily soiled cotton. The results of the laundering test are shown in Table II.
m fest "consisted smashing the scans in eminence of heavily soiled cotton. The ratings were based one-1 to fi scale with -1 having the The results indicate that the fibers containing 'poly (ethylene glycol) *distearate were inuchnnore resistant to adsorption of soil during laundering than were other abet-S:
4 Example 6 A polyesterlpolytethylene terephthalateag was pulverized and divided into 6 equal portions. Gneportiori was used as a control. An additive was added to each of the other portions. The -6 samples were converted -soeks as in Example '1.
The antiso'iling additives and the laundering characteristics of the socks are shown in Table The data indieates thatpoly(ethylene glycoli) estersof acids containing 10 or more carbons are snpeiior to esters of wids con taining less than 10 carbons. Titan: in
-. Lsundeiiug'Test Additive None 1% poly(ethylene glycol) diacetate..-- 1% radii (ethylene glycol) 'dicaproate-.. 1%:poly(ethy1ene glycol) dicaprate; 1%.poly(ethylene glycol) dilaurate- 1% pcly(etlr'yleneg'lyool) dlsteaiate 1% ipoly(ethylene glycol) dlbehen'at Example 7 A polyester [poly(l,4 cyclohexylenedimethylene terephthalate)] was pulverized and divided into eight equal parts. An additive (1% based on the weight of the polyester) was added to each part, and the polyesters were converted into socks as in Example 1.
The antisoiling additives and the laundering characteristics of the socks are shown in Table IV.
The data indicates that the molecular weight of the Example 8 A polyester [poly(1,4-cyclohexylenedimethylene terephthalate)] was pulverized and divided into four equal parts. Poly(ethylene glycol) distearate was added to each portion, and the polyesters were converted into socks as in Example 1.
The amounts of poly(ethylene glycol) distearate added to each portion and the laundering characteristics of the socks are shown in Table V.
The results indicate that at least about 0.25% of the additive is needed to impart the desired laundering characteristics.
TABLE V Additive Laundering Test 0.15% poly(ethylene glycol) dilanrate 0.25% poly (ethylene glycol) dilaurate. 0.5% poly(ethylene glycol) dilaurate 1.0% poly(ethylene glycol) dilaurate HMNN As indicated above, the particular polyester composition, the method of preparing the fiber-forming polyester polymer, and the method of spinning the polymer into fibers are not limitations on the present invention. Also, as explained in detail in the above examples, there are several useful ways in which the polyether additives of the present invention may be incorporated on and into the polyester fiber-forming polymer compositions. However, if further information is desired concerning certain of the polyesters we prefer to use the melt spinning thereof, such may be had by reference to Kibler et al. US. Patent 2,901,466. Particular reference is made to Examples 53 and 54 of this patent concerning useful methods of melt spinning certain preferred polyester compositions.
As can be seen from the foregoing description, this invention provides an especially advantageously new and useful polyester fiber having dispersed therein from about 0.25 to about 5 percent by weight, based on the weight of said polyester fiber, of a fatty acid ester of a poly(ethylene glycol), said fatty acid having 10 to 22 carbon atoms and said poly(ethylene glycol) having a molecular weight of at least 2,000.
As can further be seen from the foregoing description, this invention provides an especially advantageous new and useful process for treating polyesters, said process comprising dispersing therein from about 0.25 to about 5 percent by weight, based on the weight of said polyester, of a fatty acid ester of a poly(ethylene glycol), said fatty acid having 10 to 22 carbon atoms and said poly(ethylene glycol) having a molecular weight of at least 2,000.
As can still further be seen from the foregoing description, this invention provides an especially advantageous new and useful process for preparing a soil resistant polyester fiber, said process comprising (a) mixing a polyester powder with from about 0.25 to about 5 percent by weight, based on the weight of said polyester, of a fatty acid ester of a poly(ethylene glycol), said fatty acid having 10 to 22 carbon atoms and said poly(ethylene glycol) having a molecular weight of at least 2,000, and (b) melt spinning said soil resistant polyester fiber therefrom.
This invention has been described in detail with particular reference to preferred embodiments thereof, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention as described hereinabove and as defined in the appended claims.
I claim:
1. A process for preparing a soil resistant polyester fiber, said process comprising (a) mixing a polyester powder with from about 0.25 to about 5 percent by weight, based on the weight of said polyester, of a fatty acid ester of a poly(ethylene glycol), said fatty acid having 10 to 22 carbon atoms, said poly(ethylene glycol) having a molecular weight of at least 2,000 and said polyester being prepared from at least one diol and at least one dibasic acid, (b) melt spinning said soil resistant polyester fiber therefrom.
2. A process for preparing a soil resistant polyester fiber as defined in claim 1 wherein said fatty acid ester is poly(ethylene glycol) distearate.
3. A process for preparing a soil resistant polyester fiber as defined in claim 1 wherein said polyester is selected from the group consisting of poly(ethylene terephthalate) and poly(1,4-cyclohexylenedimethylene terephthalate).
4. A soil resistant polyester fiber prepared by a process as defined in claim 1.
References Cited UNITED STATES PATENTS 2,856,375 10/ 1958 Mikeska 260- 2,940,949 6/ 1960 Mullin 260-3l.4 3,083,187 3/1963 Stuart 260-75 3,093,612 6/ 1963 Cox 260-3 1.4 3,096,300 7/1963 Rittenhouse 2603 1.4 3,177,174 4/1965 Tirpak 260-3 1.4
JULIUS FROME, Primary Examiner.
Claims (1)
1. A PROCESS FOR PREPARING A SOIL RESISTANT POLYESTER FIBER, SAID PROCESS COMPRISING (A) MIXING A POLYESTER POWDER WITH FROM ABOUT 0.25 TO ABOUT 5 PERCENTY BY WEIGHT, BASED ON THE WEIGHT OF SAID POLYESTER, OF A FATTY ACID ESTER OF A POLY(ETHYLENE GLYCOL), SAID FATAY ACID HAVING 10 TO 22 CARBON ATOMS, SAID POLY(ETHYLENE GLYCOL) HAVING A MOLECULAR WEIGHT OF AT LEAST 2,000 AND SAID POLYESTER BEING PREPARED FROM AT LEAST ONE DIOL AND AT LEAST ONE DIBASIC ACID, (B) MELT SPINNING SAID SOIL RESISTANT POLYESTER FIBER THEREFROM.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US586671A US3355413A (en) | 1966-10-14 | 1966-10-14 | Polyester fibers resistant to resoiling during laundering |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US586671A US3355413A (en) | 1966-10-14 | 1966-10-14 | Polyester fibers resistant to resoiling during laundering |
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| US3355413A true US3355413A (en) | 1967-11-28 |
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| US586671A Expired - Lifetime US3355413A (en) | 1966-10-14 | 1966-10-14 | Polyester fibers resistant to resoiling during laundering |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3410927A (en) * | 1966-06-20 | 1968-11-12 | Monsanto Co | Polyester filaments containing polyethylene glycol esters |
| US3544658A (en) * | 1965-06-10 | 1970-12-01 | Ici Ltd | Polymeric compositions containing polyesters,polyamides and polyethers |
| US4707511A (en) * | 1985-12-17 | 1987-11-17 | General Electric Company | Thermoplastically moldable compositions |
| US5965648A (en) * | 1995-09-15 | 1999-10-12 | Eastman Chemical Company | Poly(alkylene ether)s as plasticizers and flow aids in poly (1,4-cyclohexanedimethylene terephthalate) resins |
| USH1987H1 (en) | 1998-04-23 | 2001-08-07 | Eastman Chemical Company | Non-volatile plasticizers and flow aids for polyesters |
| US6309723B1 (en) | 1992-07-29 | 2001-10-30 | Baxter International Inc. | Biomaterials with hydrophilic surfaces |
| US20080051303A1 (en) * | 2006-07-20 | 2008-02-28 | Ernst-Udo Brand | Use of polyethylene glycol esters of fatty acids as lubricants for plastics |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2856375A (en) * | 1954-08-27 | 1958-10-14 | Exxon Research Engineering Co | Fiber-forming polyesters of bisacetoxymethyl durene |
| US2940949A (en) * | 1957-08-26 | 1960-06-14 | Sun Oil Co | Composition containing polypropylene and an ester plasticizer |
| US3083187A (en) * | 1959-06-22 | 1963-03-26 | California Research Corp | Detergent polyesters |
| US3093612A (en) * | 1960-05-11 | 1963-06-11 | Monsanto Chemicals | Solutions of polyolefins and an alkoxyalkyl ester of an aliphatic monocarboxylic acid and a process for spinning same |
| US3096300A (en) * | 1958-07-10 | 1963-07-02 | Dow Chemical Co | Polymeric compositions of monovinyl aromatic hydrocarbons and synthetic rubber containing high molecular weight polyethylene glycols or monoesters of such glycols |
| US3177174A (en) * | 1961-12-07 | 1965-04-06 | Grace W R & Co | Non-static polyolefin-polyethylene glycol stearate ester composition |
-
1966
- 1966-10-14 US US586671A patent/US3355413A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2856375A (en) * | 1954-08-27 | 1958-10-14 | Exxon Research Engineering Co | Fiber-forming polyesters of bisacetoxymethyl durene |
| US2940949A (en) * | 1957-08-26 | 1960-06-14 | Sun Oil Co | Composition containing polypropylene and an ester plasticizer |
| US3096300A (en) * | 1958-07-10 | 1963-07-02 | Dow Chemical Co | Polymeric compositions of monovinyl aromatic hydrocarbons and synthetic rubber containing high molecular weight polyethylene glycols or monoesters of such glycols |
| US3083187A (en) * | 1959-06-22 | 1963-03-26 | California Research Corp | Detergent polyesters |
| US3093612A (en) * | 1960-05-11 | 1963-06-11 | Monsanto Chemicals | Solutions of polyolefins and an alkoxyalkyl ester of an aliphatic monocarboxylic acid and a process for spinning same |
| US3177174A (en) * | 1961-12-07 | 1965-04-06 | Grace W R & Co | Non-static polyolefin-polyethylene glycol stearate ester composition |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3544658A (en) * | 1965-06-10 | 1970-12-01 | Ici Ltd | Polymeric compositions containing polyesters,polyamides and polyethers |
| US3410927A (en) * | 1966-06-20 | 1968-11-12 | Monsanto Co | Polyester filaments containing polyethylene glycol esters |
| US4707511A (en) * | 1985-12-17 | 1987-11-17 | General Electric Company | Thermoplastically moldable compositions |
| US6309723B1 (en) | 1992-07-29 | 2001-10-30 | Baxter International Inc. | Biomaterials with hydrophilic surfaces |
| US5965648A (en) * | 1995-09-15 | 1999-10-12 | Eastman Chemical Company | Poly(alkylene ether)s as plasticizers and flow aids in poly (1,4-cyclohexanedimethylene terephthalate) resins |
| USH1987H1 (en) | 1998-04-23 | 2001-08-07 | Eastman Chemical Company | Non-volatile plasticizers and flow aids for polyesters |
| US20080051303A1 (en) * | 2006-07-20 | 2008-02-28 | Ernst-Udo Brand | Use of polyethylene glycol esters of fatty acids as lubricants for plastics |
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