US3418160A - Process for coating polyester fibers with a mixture of lanolin and an oily silicone - Google Patents
Process for coating polyester fibers with a mixture of lanolin and an oily silicone Download PDFInfo
- Publication number
- US3418160A US3418160A US455987A US45598765A US3418160A US 3418160 A US3418160 A US 3418160A US 455987 A US455987 A US 455987A US 45598765 A US45598765 A US 45598765A US 3418160 A US3418160 A US 3418160A
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- United States
- Prior art keywords
- lanolin
- silicone
- fibers
- fiber
- mixture
- Prior art date
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- Expired - Lifetime
Links
- 239000000835 fiber Substances 0.000 title description 48
- 239000004166 Lanolin Substances 0.000 title description 28
- 229940039717 lanolin Drugs 0.000 title description 28
- 229920001296 polysiloxane Polymers 0.000 title description 28
- 235000019388 lanolin Nutrition 0.000 title description 27
- 238000000034 method Methods 0.000 title description 15
- 239000000203 mixture Substances 0.000 title description 9
- 229920000728 polyester Polymers 0.000 title description 7
- 239000011248 coating agent Substances 0.000 title description 6
- 238000000576 coating method Methods 0.000 title description 6
- 239000004744 fabric Substances 0.000 description 23
- 239000000839 emulsion Substances 0.000 description 18
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- -1 alkyl trichlorosilane Chemical compound 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 7
- 229920002994 synthetic fiber Polymers 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 6
- 239000012209 synthetic fiber Substances 0.000 description 6
- 238000004043 dyeing Methods 0.000 description 5
- 239000005046 Chlorosilane Substances 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000009991 scouring Methods 0.000 description 4
- 229920002050 silicone resin Polymers 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 210000000085 cashmere Anatomy 0.000 description 3
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 238000005108 dry cleaning Methods 0.000 description 3
- 238000004900 laundering Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 238000009960 carding Methods 0.000 description 2
- 238000002788 crimping Methods 0.000 description 2
- MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical class CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical class [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 241000283903 Ovis aries Species 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 description 1
- 241001416177 Vicugna pacos Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- YGZSVWMBUCGDCV-UHFFFAOYSA-N chloro(methyl)silane Chemical class C[SiH2]Cl YGZSVWMBUCGDCV-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- QAEKNCDIHIGLFI-UHFFFAOYSA-L cobalt(2+);2-ethylhexanoate Chemical compound [Co+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O QAEKNCDIHIGLFI-UHFFFAOYSA-L 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical class COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000011133 lead Chemical class 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 210000000050 mohair Anatomy 0.000 description 1
- 125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BILPUZXRUDPOOF-UHFFFAOYSA-N stearyl palmitate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC BILPUZXRUDPOOF-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000004758 synthetic textile Substances 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
Definitions
- ABSTRACT OF THE DISCLOSURE The process for imparting a durable, aestheticallypleasing cashmere-like feel to polyester fabrics which comprises coating the fibers of the fabric before being made into yarn with an aqueous emulsion of lanolin and a specific oily silicone with the weight ratio of silicone to lanolin being within the range of 1.5 to 3, and then heating the coated fibers to cross-link the silicone and to provide the improved durable aesthetics.
- This invention is concerned with the surface treatment of synthetic fibers. It is particularly concerned with the surface treatment of polyester fibers to add softness and slickness to the fibers.
- Certain natural fibers such as cashmere, lambs Wool, mohair and alpaca have surface characteristics which make them especially suitable for the manufacture of fabrics with outstanding aesthetic values. These fabrics have a smooth, soft, slick feel or hand and good draping qualities which make them luxurious. The synthetic fibers do not possess these qualities to a high degree unless the surfaces of the fibers are modified after spinning.
- This object is accomplished in the present invention by applying to the fibers, preferably in the form of a tow before cutting into staple, a finish consisting of lanolin and a silicone resin which further polymerizes on the fiber.
- the fibers be dyeable. Not only must they take up the dyestutf under normal conditions of dyeing but they should dye uniformly, free of streaks or blotches. And since most fabrics go through hot-wet treatments as in dyeing, usually in the presence of detergents, it is essential that any finish which is to modify the properties of the final fabric must be fast to these wet treatments. Also, when the fabrics are used, especially if used in garments, they will frequently be laundered or dry-cleaned. The desirable finish must be durable to such treatments if the full benefits of the finish are to be realized.
- the finish of the present invention which meets these rigid requirements, comprises a mixture of 1.5 to 3 parts of certain silicone resins per part of lanolin. About 5 to emulsions of these materials are used. Silicone alone ICC or in higher ratios than stated imparts an oily feel to the fibers and results in poor fiber processability due to lack of yarn cohesion. Lower ratios of silicone to lanolin give finishes with a less pleasant hand and which are not durable to laundering and dry-cleaning. Satisfactory results are obtained when about 0.5 to 2.0%, and preferably 0.75 to 1.50%, of the finish is applied to the fibers.
- the preferred method of carrying out this invention consists of passing a tow of the synthetic fiber through an emulsion of the silicone resin and lanolin, squeezing out the excess emulsion, crimping the fibers in a stufferbox crimper While still wet, either cutting the wet tow into staple or first drying and then cutting. After drying, it is heated further to cross-link the resin on the fiber. The staple is then converted to fabric by the usual methods.
- Lanolin is the protective covering on sheeps wool and is recovered in wool scouring. It is widely used in cosmetics and its use as a fiber or fabric finish is disclosed in a number of patents, notably Canadian Patents 540,273 and 581,754 and German Patent 1,004,584.
- the emulsion of lanolin and silicone can be readily prepared by the use of a small amount of any of a number of surface-active agents of the anionic, cationic or non-ionic type.
- the silicone must be cross-linkable after it is applied to the fiber and this property is gained by copolymerizing the following silanes: alkyl trichlorosilane, dialkyl dichlorosilane, trialkyl chlorosilane and alkyl hydrogen dichlorosilane which are represented by the following formulas, respectively: R SiCl, R SiCl RSiCl and RHSiCl
- a range of silicones can be made by the following procedure: One or more of the chlorosilanes shown above, preferably the methyl chlorosilanes and methyl hydrogen chlorosilanes, is dissolved in dry benzene using parts of benzene to 1 part of the silane.
- the benzene solution is cooled to 20 C. and 67.5 parts of isopropyl alcohol are added over a period of several minutes with stirring. Then 75 parts of water are added slowly. The polymer is washed several times with water; then the benzene is distilled off at a pressure of 3 mm. and a temperature up to C.
- the final product is an oily polymer and when alkylhydrogen chlorosilane is included in the silane mixture, the resulting polymer is capable of condensing further by virtue of the hydrogen atoms on the silicon atoms.
- the polymers made by this process can be represented by the following general formula:
- m should have a value of 1.0 to 1.75 and n a value of 0.25 to 1.25; R is usually CH Commercial silicones sold under the trade names Decetex 104 and ET53 17 are also satisfactory for use in this invention.
- a catalyst is used with the silicone to hasten its further polymerization.
- Traces of certain metal salts of organic acids serve as catalysts. Cobalt, manganese and lead salts of 6- to lO-carbon fatty acids or branched-chain acids are satisfactory. Salts of 2-ethylhexanoic acid are widely used and commercial catalysts are available for the silicone resins. Organic amines such as morpholine are also suitable catalysts.
- Lanolin can be used as such or in the form of certain derivatives such as the reaction products of lanolin and ethylene oxide.
- the polyhydroxyethyl lanolin is more readily emulsified than lanolin itself.
- certain commercial lanolin emulsions can be used such as Lanolized WW. sold by Scholler Brothers.
- the lanolin and the silicone are mixed and added to Water containing an emulsifying agent, with vigorous stirring.
- the emulsifying agent can be added to the lanolin and silicone and this mixture then stirred into water.
- Anionic or nonionic emulsifying agents are preferred.
- Long chain alcohol sulfates, long chain alkyl sulfonates, alkylphenolpolyethylene glycols, sorbitan mono stearate or oleate, are types that can be used.
- Small amounts of a long-chain unsaturated alcohol such as hexadecenyl alcohol or octadecenyl alcohol when used with the emulsifying agent will improve the ease of forming the emulsion.
- the emulsion of silicone and lanolin is applied to a tow of the fiber to be treated by running the tow through the diluted emulsion, and then through squeeze rolls to remove excess emulsion.
- the coated tow is crimped by passing it through a stutfer-box crimper to impart about 6 to 15, preferably 8 to 10, crimps per inch.
- the tow is then dried in a relaxed state and cured at 140 C. for 6 minutes to cross-link the silicone. It is next cut into 3-inch staple.
- the cured staple fiber is then carded and spun on the worsted system and the yarn is knit into a fabric; the aesthetics are determined before and after washing, dyeing, and dry-cleaning.
- the following examples will illustrate the invention in more detail.
- a copolymer is made by esterifying (by ester interchange) ethylene glycol and a mixture of terephthalic acid dimethyl ester and sulfonated isophthalic acid dimethyl ester containing 2 mol percent of the latter.
- the copolymer ester is made by the method disclosed in US. Patent 3,018,272 to Gritfing and Remington. This is a basic-dyeable copolymer.
- the copolymer is spun into a 3 denier per filament fiber by conventional melt spinning and drawing methods.
- a 15,000 denier tow of this fiber is passed, at 25 yards per minute through an aqueous emulsion containing, by weight, 3.5% silicone, 3.5% lanolin and 0.05% cobalt 2- ethylhexanoate.
- the silicone used in this example has a ratio of SiH to SiCH groups of 26 to 74.
- the emulsion is formed by adding the silicone and the lanolin to water containing 0.2 part of an emulsifying agent made by first reacting a mixture of octadecyl, octadecenyl, hexadecyl and hexadecenyl alcohols with 6 mols ethylene oxide, then esterifying with sulfuric acid. The sulfate ester is poured into a solution of sodium hydroxide to form the sodium salt,
- the emulsion is formed by adding 10 parts of the silicone-lanolin mixture to 100 parts of water containing the emulsifying agent. After emulsification, more water is added to give a silicone content and a lanolin content of 3.5% each. The catalyst is added to the diluted emulsion with the temperature not over 40 C.
- the treated tow is then passed through squeeze rolls (leaving parts of the emulsion on 100 parts of fiber or a loading of about 1.4% of solids on the fiber). It is next passed through a stuffer-box crimper to impart about 8 to 10 crimps per inch and dried in a relaxed state on a belt passing through an oven. The dried tow is cured 6 minutes at 140 C. then cut into 3-inch staple and the latter is carded and spun on the worsted system to yield a $5 worsted count yarn with 7 turns per inch. No difliculty is encountered in carding and spinning this fiber.
- the yarn is knit into a 22 course per. inch fabric.
- the aesthetics of the fabric are judged by a panel of judges, in the gray state, after scouring and after dyeing.
- the hand of the gray fabric is found to be soft and smooth but slightly greasy and somewhat lacking in slickness. After scouring and after dyeing, the fabric is slightly improved but not sufiiciently slick.
- Example II The same fiber prepared in Example I is treated with an aqueous emulsion containing, by weight, 4.1% silicone and 2.7% lanolin. About 1.4% of finish, on the dry fiber weight, is left on the fiber after squeezing out the excess. After processing as in Example I, a fabric of improved slickness is obtained which closely approximates the hand of cashmere. The slickness and softness of this fabric is not appreciably diminished by 5 scourings in soap for 20 minutes at 40 C.
- This process is especially suitable for finishing polyester fibers such as those of poly(ethylene terephthalate) or polyester formed of dicarboxylic acid other then terephthalic acid, but it will have merit on other synthetic fibers.
- the finish is useful, not only for providing a pleasant and luxurious feel to fabrics made from the fibers but also to facilitate the processing of the fibers into yarns.
- the fibers possess the optimum degree of cohesiveness and the correct slip to make them highly satisfactory for carding and spinning where uniform yarns are desired.
- Knit fabrics made from fibers treated by the process of the present invention can be napped to make fur-like fabrics which are especially suitable for fur ironing to straighten the fur pile.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
United States Patent 3,418,160 PROCESS FOR COATING POLYESTER FIBERS WITH A MIXTURE OF LANOLIN AND AN OILY SILICONE Steven Abashian, Kinston, N.C., assignor to E. I. du Pont de Nemours and Company, Wilmington, Del., a corporation of Delaware No Drawing. Filed May 14, 1965, Ser. No. 455,987 2 Claims. (Cl. 117138.8)
ABSTRACT OF THE DISCLOSURE The process for imparting a durable, aestheticallypleasing cashmere-like feel to polyester fabrics which comprises coating the fibers of the fabric before being made into yarn with an aqueous emulsion of lanolin and a specific oily silicone with the weight ratio of silicone to lanolin being within the range of 1.5 to 3, and then heating the coated fibers to cross-link the silicone and to provide the improved durable aesthetics.
This invention is concerned with the surface treatment of synthetic fibers. It is particularly concerned with the surface treatment of polyester fibers to add softness and slickness to the fibers.
Certain natural fibers such as cashmere, lambs Wool, mohair and alpaca have surface characteristics which make them especially suitable for the manufacture of fabrics with outstanding aesthetic values. These fabrics have a smooth, soft, slick feel or hand and good draping qualities which make them luxurious. The synthetic fibers do not possess these qualities to a high degree unless the surfaces of the fibers are modified after spinning.
It is an object of the present invention to modify the surface of synthetic fibers to impart softness and slickness to the fibers to give them the aesthetic qualities of the more luxurious of the natural fibers.
This object is accomplished in the present invention by applying to the fibers, preferably in the form of a tow before cutting into staple, a finish consisting of lanolin and a silicone resin which further polymerizes on the fiber.
The modification of the surface of a fiber at the point of manufacture to produce some particular effect in fabrics prepared from the fiber presents many problems. First it is necessary that the fiber process well in the operations necessary to convert it into a fabric. If it is cut into staple, the staple should card well without forming maps and without fouling up the cards. If the tow is converted to sliver by the Turbo process or the Pacific Converter process, it should provide a sliver with good drafting properties and not produce an excessive amount of short fibers or loose fibers fly. Many finishes which impart softness, smoothness and slickness to fibers are not satisfactory because the staple fibers will not card.
A further requirement is that the fibers be dyeable. Not only must they take up the dyestutf under normal conditions of dyeing but they should dye uniformly, free of streaks or blotches. And since most fabrics go through hot-wet treatments as in dyeing, usually in the presence of detergents, it is essential that any finish which is to modify the properties of the final fabric must be fast to these wet treatments. Also, when the fabrics are used, especially if used in garments, they will frequently be laundered or dry-cleaned. The desirable finish must be durable to such treatments if the full benefits of the finish are to be realized.
The finish of the present invention, which meets these rigid requirements, comprises a mixture of 1.5 to 3 parts of certain silicone resins per part of lanolin. About 5 to emulsions of these materials are used. Silicone alone ICC or in higher ratios than stated imparts an oily feel to the fibers and results in poor fiber processability due to lack of yarn cohesion. Lower ratios of silicone to lanolin give finishes with a less pleasant hand and which are not durable to laundering and dry-cleaning. Satisfactory results are obtained when about 0.5 to 2.0%, and preferably 0.75 to 1.50%, of the finish is applied to the fibers.
The preferred method of carrying out this invention consists of passing a tow of the synthetic fiber through an emulsion of the silicone resin and lanolin, squeezing out the excess emulsion, crimping the fibers in a stufferbox crimper While still wet, either cutting the wet tow into staple or first drying and then cutting. After drying, it is heated further to cross-link the resin on the fiber. The staple is then converted to fabric by the usual methods.
Lanolin is the protective covering on sheeps wool and is recovered in wool scouring. It is widely used in cosmetics and its use as a fiber or fabric finish is disclosed in a number of patents, notably Canadian Patents 540,273 and 581,754 and German Patent 1,004,584.
The emulsion of lanolin and silicone can be readily prepared by the use of a small amount of any of a number of surface-active agents of the anionic, cationic or non-ionic type. The silicone must be cross-linkable after it is applied to the fiber and this property is gained by copolymerizing the following silanes: alkyl trichlorosilane, dialkyl dichlorosilane, trialkyl chlorosilane and alkyl hydrogen dichlorosilane which are represented by the following formulas, respectively: R SiCl, R SiCl RSiCl and RHSiCl A range of silicones can be made by the following procedure: One or more of the chlorosilanes shown above, preferably the methyl chlorosilanes and methyl hydrogen chlorosilanes, is dissolved in dry benzene using parts of benzene to 1 part of the silane. The benzene solution is cooled to 20 C. and 67.5 parts of isopropyl alcohol are added over a period of several minutes with stirring. Then 75 parts of water are added slowly. The polymer is washed several times with water; then the benzene is distilled off at a pressure of 3 mm. and a temperature up to C. The final product is an oily polymer and when alkylhydrogen chlorosilane is included in the silane mixture, the resulting polymer is capable of condensing further by virtue of the hydrogen atoms on the silicon atoms.
The polymers made by this process can be represented by the following general formula:
For purposes of this invention m should have a value of 1.0 to 1.75 and n a value of 0.25 to 1.25; R is usually CH Commercial silicones sold under the trade names Decetex 104 and ET53 17 are also satisfactory for use in this invention.
More wash-fast results are obtained if a catalyst is used with the silicone to hasten its further polymerization. Traces of certain metal salts of organic acids serve as catalysts. Cobalt, manganese and lead salts of 6- to lO-carbon fatty acids or branched-chain acids are satisfactory. Salts of 2-ethylhexanoic acid are widely used and commercial catalysts are available for the silicone resins. Organic amines such as morpholine are also suitable catalysts.
Lanolin can be used as such or in the form of certain derivatives such as the reaction products of lanolin and ethylene oxide. The polyhydroxyethyl lanolin is more readily emulsified than lanolin itself. Also certain commercial lanolin emulsions can be used such as Lanolized WW. sold by Scholler Brothers.
On carrying out this invention the lanolin and the silicone are mixed and added to Water containing an emulsifying agent, with vigorous stirring. Alternately, the emulsifying agent can be added to the lanolin and silicone and this mixture then stirred into water. Anionic or nonionic emulsifying agents are preferred. Long chain alcohol sulfates, long chain alkyl sulfonates, alkylphenolpolyethylene glycols, sorbitan mono stearate or oleate, are types that can be used. Small amounts of a long-chain unsaturated alcohol such as hexadecenyl alcohol or octadecenyl alcohol when used with the emulsifying agent will improve the ease of forming the emulsion.
The emulsion of silicone and lanolin is applied to a tow of the fiber to be treated by running the tow through the diluted emulsion, and then through squeeze rolls to remove excess emulsion. The coated tow is crimped by passing it through a stutfer-box crimper to impart about 6 to 15, preferably 8 to 10, crimps per inch. The tow is then dried in a relaxed state and cured at 140 C. for 6 minutes to cross-link the silicone. It is next cut into 3-inch staple.
The cured staple fiber is then carded and spun on the worsted system and the yarn is knit into a fabric; the aesthetics are determined before and after washing, dyeing, and dry-cleaning. The following examples will illustrate the invention in more detail.
EXAMPLE I A copolymer is made by esterifying (by ester interchange) ethylene glycol and a mixture of terephthalic acid dimethyl ester and sulfonated isophthalic acid dimethyl ester containing 2 mol percent of the latter. The copolymer ester is made by the method disclosed in US. Patent 3,018,272 to Gritfing and Remington. This is a basic-dyeable copolymer.
The copolymer is spun into a 3 denier per filament fiber by conventional melt spinning and drawing methods. A 15,000 denier tow of this fiber is passed, at 25 yards per minute through an aqueous emulsion containing, by weight, 3.5% silicone, 3.5% lanolin and 0.05% cobalt 2- ethylhexanoate.
The silicone used in this example has a ratio of SiH to SiCH groups of 26 to 74. The emulsion is formed by adding the silicone and the lanolin to water containing 0.2 part of an emulsifying agent made by first reacting a mixture of octadecyl, octadecenyl, hexadecyl and hexadecenyl alcohols with 6 mols ethylene oxide, then esterifying with sulfuric acid. The sulfate ester is poured into a solution of sodium hydroxide to form the sodium salt,
- carefully avoiding a pH below 7.
The emulsion is formed by adding 10 parts of the silicone-lanolin mixture to 100 parts of water containing the emulsifying agent. After emulsification, more water is added to give a silicone content and a lanolin content of 3.5% each. The catalyst is added to the diluted emulsion with the temperature not over 40 C.
The treated tow is then passed through squeeze rolls (leaving parts of the emulsion on 100 parts of fiber or a loading of about 1.4% of solids on the fiber). It is next passed through a stuffer-box crimper to impart about 8 to 10 crimps per inch and dried in a relaxed state on a belt passing through an oven. The dried tow is cured 6 minutes at 140 C. then cut into 3-inch staple and the latter is carded and spun on the worsted system to yield a $5 worsted count yarn with 7 turns per inch. No difliculty is encountered in carding and spinning this fiber.
The yarn is knit into a 22 course per. inch fabric. The aesthetics of the fabric are judged by a panel of judges, in the gray state, after scouring and after dyeing. The hand of the gray fabric is found to be soft and smooth but slightly greasy and somewhat lacking in slickness. After scouring and after dyeing, the fabric is slightly improved but not sufiiciently slick.
4 EXAMPLE II The same fiber prepared in Example I is treated with an aqueous emulsion containing, by weight, 4.1% silicone and 2.7% lanolin. About 1.4% of finish, on the dry fiber weight, is left on the fiber after squeezing out the excess. After processing as in Example I, a fabric of improved slickness is obtained which closely approximates the hand of cashmere. The slickness and softness of this fabric is not appreciably diminished by 5 scourings in soap for 20 minutes at 40 C.
This process is especially suitable for finishing polyester fibers such as those of poly(ethylene terephthalate) or polyester formed of dicarboxylic acid other then terephthalic acid, but it will have merit on other synthetic fibers. The finish is useful, not only for providing a pleasant and luxurious feel to fabrics made from the fibers but also to facilitate the processing of the fibers into yarns. The fibers possess the optimum degree of cohesiveness and the correct slip to make them highly satisfactory for carding and spinning where uniform yarns are desired.
Knit fabrics made from fibers treated by the process of the present invention can be napped to make fur-like fabrics which are especially suitable for fur ironing to straighten the fur pile.
The following table gives additional data showing the preferred ratio of components of the finish.
Finish composition Subjective evaluation Remarks cleaning.
50/50 silic0ne/lano1in Slightly greasy Durable to laundering,
not durable to dry cleanin Durable to laundering 60/40 silicone/lanolin. Smooth and slick,
and dry cleaning.
closely approximates cashmere. 75/25 silicone/lanolin Smooth and slick but inferior to 60/40. /20 s1l1cone/lanol1n. Slick but too oily From the foregoing discussion, description and data, it is evident that the present discovery provides a significant advance in the art of improving the aesthetics of synthetic fibers. While the invention has been described with regard to specific detail, it will be appreciated that changes can be made without departing from its scope.
What is claimed is:
1. In the production of synthetic fabrics of fibers of a polyester polymer including the steps of extruding the polymer through a spinneret having capillaries, quenching the extruded polymer to form filaments, combining the filaments to form a tow, drawing and crimping the filaments, making a yarn of the tow, and then forming said fabric by knitting or weaving; the improvement for imparting a durable aesthetically pleasing cashmere-like hand to the fabric which comprises coating the fibers of the tow before making the yarn with an aqueous emulsion of lanolin and an oily silicone having the unit formula Where m has a value of 1.0 to 1.75, n has a value of 0.25 to 1.25 and R is lower alkyl, there being 1.5 to 3 parts by weight of silicone per part of lanolin in the emulsion; said fibers being coated with suflicient solution to provide a coating of from about 0.5 to about 2 percent by weight, based on the fibers, of the combined lanolin and silicone; and then heating the coated fibers to cross-link the silicone; said aqueous solution being further characterized as having a catalytic amount of a co'baltic catalyst to enhance silicone polymerization and provide a more wash-fast coating.
2. The process as in claim 1 wherein the coated fibers 2,832,518 4/ 1958 Doyle et al. are heated to a temperature af about 140 C. for a suf- 3,271,189 9/ 1966 Hofrnann. fic1ent tune mterval to cross-hnk the slhcone. FOREIGN PATENTS References Cited 5 540,273 4/ 1957 Canada. UNITED STATES PATENTS WILLIAM D. MARTIN, Primary Examiner.
2,437,263 3/1948 M nning 264210 X T. G. DAVIS, Assistant Examiner. 2,875,019 2/1959 Spohn et a1. 264210 X U S C1 X R 2,918,346 12/1959 Paulsen 264210 X 2,934,400 4/1960 Siggel et a1. 264210 10 117139.5, 161; 264-168
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US455987A US3418160A (en) | 1965-05-14 | 1965-05-14 | Process for coating polyester fibers with a mixture of lanolin and an oily silicone |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US455987A US3418160A (en) | 1965-05-14 | 1965-05-14 | Process for coating polyester fibers with a mixture of lanolin and an oily silicone |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3418160A true US3418160A (en) | 1968-12-24 |
Family
ID=23810991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US455987A Expired - Lifetime US3418160A (en) | 1965-05-14 | 1965-05-14 | Process for coating polyester fibers with a mixture of lanolin and an oily silicone |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3418160A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3807273A (en) * | 1972-05-24 | 1974-04-30 | Sutures Inc | Method of making pliable, dyed and braided polyester sutures |
| US4397985A (en) * | 1980-04-04 | 1983-08-09 | Allied Corporation | Polyester yarn finish composition |
| US4579964A (en) * | 1983-03-31 | 1986-04-01 | Union Carbide Corporation | Alkoxysilyl functional silicones |
| EP0356827A3 (en) * | 1988-08-31 | 1992-01-02 | Bayer Ag | Lubricant based on polyorganosiloxane |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2437263A (en) * | 1948-03-09 | Fred w | ||
| CA540273A (en) * | 1957-04-30 | L. Copenhaver Dwight | Textile treating | |
| US2832518A (en) * | 1953-09-29 | 1958-04-29 | Doyle | Process of applying lanolin finish to nylon hosiery and heat setting the hosiery andproducts produced therefrom |
| US2875019A (en) * | 1956-01-17 | 1959-02-24 | Firestone Tire & Rubber Co | Method for producing crimped filaments |
| US2918346A (en) * | 1956-08-07 | 1959-12-22 | Du Pont | Process of orienting a dense tow of polymeric ester filaments by two step hot aqueous bath treatments |
| US2934400A (en) * | 1955-03-19 | 1960-04-26 | Glanzstoff Ag | Process of manufacturing fibers of polyethylene terephthalate |
| US3271189A (en) * | 1962-03-02 | 1966-09-06 | Beaunit Corp | Process of treating synthetic fibers |
-
1965
- 1965-05-14 US US455987A patent/US3418160A/en not_active Expired - Lifetime
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2437263A (en) * | 1948-03-09 | Fred w | ||
| CA540273A (en) * | 1957-04-30 | L. Copenhaver Dwight | Textile treating | |
| US2832518A (en) * | 1953-09-29 | 1958-04-29 | Doyle | Process of applying lanolin finish to nylon hosiery and heat setting the hosiery andproducts produced therefrom |
| US2934400A (en) * | 1955-03-19 | 1960-04-26 | Glanzstoff Ag | Process of manufacturing fibers of polyethylene terephthalate |
| US2875019A (en) * | 1956-01-17 | 1959-02-24 | Firestone Tire & Rubber Co | Method for producing crimped filaments |
| US2918346A (en) * | 1956-08-07 | 1959-12-22 | Du Pont | Process of orienting a dense tow of polymeric ester filaments by two step hot aqueous bath treatments |
| US3271189A (en) * | 1962-03-02 | 1966-09-06 | Beaunit Corp | Process of treating synthetic fibers |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3807273A (en) * | 1972-05-24 | 1974-04-30 | Sutures Inc | Method of making pliable, dyed and braided polyester sutures |
| US4397985A (en) * | 1980-04-04 | 1983-08-09 | Allied Corporation | Polyester yarn finish composition |
| US4579964A (en) * | 1983-03-31 | 1986-04-01 | Union Carbide Corporation | Alkoxysilyl functional silicones |
| EP0356827A3 (en) * | 1988-08-31 | 1992-01-02 | Bayer Ag | Lubricant based on polyorganosiloxane |
| US5171464A (en) * | 1988-08-31 | 1992-12-15 | Bayer Aktiengesellschaft | Lubricant based on polyorganosiloxanes |
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