US2299535A - Yarn conditioning process and composition therefor - Google Patents
Yarn conditioning process and composition therefor Download PDFInfo
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- US2299535A US2299535A US246512A US24651238A US2299535A US 2299535 A US2299535 A US 2299535A US 246512 A US246512 A US 246512A US 24651238 A US24651238 A US 24651238A US 2299535 A US2299535 A US 2299535A
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- yarn
- conditioning
- cellulose
- lubricating
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- 230000003750 conditioning effect Effects 0.000 title description 27
- 239000000203 mixture Substances 0.000 title description 20
- 238000000034 method Methods 0.000 title description 13
- 239000004753 textile Substances 0.000 description 26
- 230000001050 lubricating effect Effects 0.000 description 23
- 239000003795 chemical substances by application Substances 0.000 description 22
- 238000009940 knitting Methods 0.000 description 22
- 238000009987 spinning Methods 0.000 description 20
- 125000001424 substituent group Chemical group 0.000 description 17
- 229920002301 cellulose acetate Polymers 0.000 description 16
- 238000009941 weaving Methods 0.000 description 16
- 229920002678 cellulose Polymers 0.000 description 15
- 239000001913 cellulose Substances 0.000 description 14
- 239000002904 solvent Substances 0.000 description 11
- 150000003017 phosphorus Chemical class 0.000 description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 8
- 125000003277 amino group Chemical group 0.000 description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
- 239000001301 oxygen Substances 0.000 description 8
- 229910052717 sulfur Chemical group 0.000 description 8
- 239000011593 sulfur Chemical group 0.000 description 8
- 239000000314 lubricant Substances 0.000 description 7
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- -1 polyalkoxy Chemical group 0.000 description 6
- 239000004902 Softening Agent Substances 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000008158 vegetable oil Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000010775 animal oil Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 2
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 2
- 240000007817 Olea europaea Species 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 239000012237 artificial material Substances 0.000 description 2
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 2
- 229920006218 cellulose propionate Polymers 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- REOJLIXKJWXUGB-UHFFFAOYSA-N mofebutazone Chemical group O=C1C(CCCC)C(=O)NN1C1=CC=CC=C1 REOJLIXKJWXUGB-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- FZHNJMKVRJJKBK-UHFFFAOYSA-N 1-dichlorophosphorylpiperidine Chemical compound ClP(Cl)(=O)N1CCCCC1 FZHNJMKVRJJKBK-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- LYBYLVMWDKBFTO-UHFFFAOYSA-N bis(2-ethoxyethyl) hydrogen phosphate Chemical compound CCOCCOP(O)(=O)OCCOCC LYBYLVMWDKBFTO-UHFFFAOYSA-N 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229940059904 light mineral oil Drugs 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000002759 woven fabric Substances 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
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
- D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
- D06M13/292—Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2904—Staple length fiber
- Y10T428/2907—Staple length fiber with coating or impregnation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2965—Cellulosic
Definitions
- This invention relates to the conditioning of textile yarns and more particularly to the conditioning of filaments and yarns composed of organic derivatives of cellulose such as cellulose acetate, cellulose propionate, cellulose acetate propionate, and cellulose acetate butyrate, to render them more amenable to textile operations such as knitting and the like.
- softening agents such as polyhydric alcohols and similar agents as ingredients of yarn conditioning or lubricating formulas, generally in connection with mineral, animal or vegetable oils. It has been found, however, that most of the known softening agents and the various formulas containing them have certain drawbacks, one of the most serious of which is high vapor pressure, and in some cases too drastic a solvent action on theyarn. Many of such agents possess slight or insufficient solvent power for the lubricants with which they are used, and it s accordingly necessary to employ blending agents or emulsifying agents in order to obtain operable yarn treating formulas.
- This invention has as its principal object to provide an entirely new class of yarn conditioning agents which are particularly adapted for the treatment of yarns composed of or containing organic derivatives of cellulose and capable of lubricating, softening and rendering such yarns more amenable to knitting and other textile operations.
- a further and specific object is to provide a class of conditioning agents which augment or assist the lubricating action of varand capable of employment in a variety of textile operations where complicated designs or stitches are employed.
- Another object is to provide an improved type of yarn which is especially amenable to textile operations including circular knitting, weaving, spinning and-the like.
- :c is a substituent selected from the group consisting of oxygen and sulfur
- R is a substituent selected from the group consisting of alkyl and aryl groups, which groups may be substituted with other groups including alkoxy, polyalkoxy, tetrahydrofurfuryloxy, etc.
- B is a substituent selected from the group consisting of and wherein B is a substituted amino group, OR, -0 alkyl, o-aryl and B, and wherein B is a substituted amino group, may be used as yarn conditioning agents and particularly as softening agents, with or without the addition of animal, mineral, or vegetable oils, in the treatment of yarns composed of or containing organic derivatives of cellulose.
- these compounds when employed as described in the detailed examples set forth below have a slight solvent and/or softening action on cellulose organic derivative yarns which renders such yarns soft and pliable without at the same time having too drastic an action thereon.
- these compounds may be applied directly to the yarn during or after spinning, or may be added to the spinning solution itself.
- these compounds have exceptional solvent powers which enable them to dissolve mineral oils and blown and unblown, drying and semi-drying, vegetable and animal oils and accordingly they may be, and preferably are, employed as ingredients of yarn conditioning or lubricating formulas in conjunction with agents which function wholly. or partially as lubricants.
- the amount of conditioningliquid applied may vary from e25% by weight of the yarn, and if the yarn is intended for weaving, the amount of liquid applied may vary from 1-5% by weight of the yarn.
- Example 4 A conditioning liquid is made up as follows:
- the filaments thus pro- 1 quizd are wound, or-twlsted and wound.
- Yarns produced from filaments, thus prepared are pliable and suitable for knitting.
- compositions may be applied to the yarn intended for use in circular knitting by means of a bath, wick, spray, roller, pad or any suitable means.
- the amount of conditioning liquid applied may vary between 5-25% by weight of the yarn. Usually, however, the
- the conditioning agents of our invention may be applied by a wide variety of methods.
- the agent as an ingredient of the spinning dope from which the filaments are formed, the amount of the agent 50 employed depending upon a number of factors, such as the particular cellulose derivative used in making the yarn, th'e solvent or solvent combination used in making up the spinning solution, and the degree of softness or pliability desired in the yarn,etc.
- the conditioning agent is to be applied to theyarn after spinning, this may be done by bringing the yarn in contact with a wick, roll, or felt wet therewith, or the liquid may be applied by immersion, spray, or otherwise.
- the particular point at which the liquid is applied may vary. It may, for example, be applied to the yarn inside or outsidecthe spinning cabinet, between the guide and godet roll, between the godet or other roll or guide and the point of winding and/or twisting. In some cases, the liquid may even be applied to the yarn after winding onto cones, spools, bobbins, or the like or by the socalled bobbin to bobbin method. In the case of staple fiber manufacture, the liquid may be applied to the yarn prior to, or after cutting into staple lengths.
- the amount of the agent so employed will vary widely depending upon the results desired, the specific nature of the material to which the agent is applied, the use to which the yarn is eventually to be put and other factors. For example, in a given case where a cellulose organic acid ester yarn such as a yarn composed of cellulose acetate, is intended for knitting, about 4 to 25% or more by weight, based on the weight of the dry yarn, may be satisfactory, while if the yarn is intended for weaving, the amount may vary between about 1 and 5%.
- compositions containing specific percentages of thevarious ingredients may vary widely depending upon the particular purpose for which the composition is intended. For example, if it is desired to control the solvent or softening action of the conditioning agent, the amount of the agent may be adjusted as, for example, by reducing the amount of the agent and correspondingly increasing the amount of oil or other ingredient.
- the conditioning agents and formulas described herein are applicable to the conditioning of many other types of cellulose derivative yarns such as those composed of or containing cellulose propionate, cellulose butyrate, cellulose acetate propionate, cellulose acetate butyrate, ethyl cellulose, methyl cellulose, benzyl cellulose and others, as well as to the conditioning of silk, wool, cotton, viscose and other natural or artificial materials.
- yarn as used herein and in the claims is to be understood as including a single filament, a plurality of filaments associated into the form of a thread, either of high or low twist,
- composite threads composed of a mixture of natural and artificial filaments or a composite thread formed by twisting together individual strands of natural or artificial materials, as well as cut staple fibers produced from natural and/or artificial filaments or threads and spun yarn produced from such stable fibers.
- the yarn conditioning agents of our invention are exceptionally good solvents for a wide variety of mineral, blown and unblown, drying and semi-drying animal and vegetable oils such as cottonseed, olive, castor, neats-foot, sperm and other oils. This enables them to be used with any of such oils in making up a variety of yarn treating formulas of varying composition.
- the yam conditioning method and compositions of our invention possess many outstanding advantages.
- the fundamental and outstanding characteristic of the agents employed in accordance with the invention is their ability to soften yarns, especially those composed of or containing organic derivatives of cellulose such as cellulose acetate and render them soft and pliable and amenable to various textile operations, especially operations such'as those involved in weaving and knitting where complicated designs or stitches are employed, without too drastic an action on the yarn material.
- Another outstanding characteristic of these compounds is their exceptional solvent power for a wide variety of mineral, animal, and. vegetable oils and their ability to act as lubricating assistants inconjunction with these oils when applied to such yarns.
- a is a substituent selected from the group consisting of oxygen and sulfur;
- R is an alkoxy alkyl group,
- B is a substituent selected from the group consisting of OR, -o-alkyl, -o-aryl and B; and
- B is a substituted amino group.
- a is a substituent selected from the group consisting of oxygen and sulfur;
- R is an alkoxyalkyl group, 33 is a substituent selected from the group consisting of OR, -o-alkyl, -o-aryl and B; and B is a substituted amino group.
- s is a substituent selected from the group consisting of oxygen and sulfur; R is an alkoxy: alkyl group, B is a substituent selected from. the group consisting of OR, -o-alkyl, -o-aryl and B; and B is a substituted amino group.
- the process of conditioning yarn composed of or containing cellulose acetate to render it more amenable to textile operations including knitting, weaving, spinning, and the like which comprises applying thereto a lubricating and" softening composition containing as its essential lubricating and softening component p'-ethoxyp-ethoxyethyl-methyl ester 9f thio diethyl phosphamic acid.
- a is a substituent selected from the group consisting of oxygen and sulfur;
- R is an alkoxyalkyl group,
- B is a substituent selected from the group consisting of OR, -o-alkyl, -o-ary1 and B; and
- B is a substituted amino group
- Textile yarns composed of or containing organic derivatives of cellulose amenable to textile operations including knitting, weaving, spinning, and the like impregnated with a lubricating and softening composition containing as its essential lubricating and softening component a derivative of phosphorus having the general formula:
- a is a substituent selected from the group consisting of oxygen and sulfur; R, is an alkoxyalkyl group, B is a substituent selected from the group consisting of OR, -o-alkyl, -o-aryl and B; and B is a substituted amino group.
- Textile yarns composed of orcontaining cellulose acetate amenable to textile operations including knitting, weaving, spinning, and the like impregnated with a lubricating and softening composition containing as its essential lubricating and softening component a derivative of phosphorus having the general formula:
- a is a substituent selected from the group consisting of oxygen and sulfur;
- R is an alkoxyalkyl group,
- B is a substituent selected from the group consisting of OR, o-alkyl, -o-aryl and B; and
- B is a substituted amino group.
- Textile yarns composed of or containing cellulose aceate amenable to-textile operations including knitting, weaving, spinning, and the like, impregnated with a lubricant comprising dioctadecyl ester of di-B-methoxyethyl phosphamate.
- Textile yarns composed of or containing cellulose acetate amenable' to textile operations including knitting, weaving, spinning, and the like, impregnated with a lubricant pomprising di-p-methoxy ethyl ester of monobutyl phosphamate.
- Textile yarns composed of or containing cellulose acetate amenable to textile operations including knitting, weaving, spinning, and the like, impregnated with a. lubricant comprising p-ethoxy-fl-ethoxyethyl-methyl ester of thio diethyi phosphamic acid.
- a textile yarn lubricating and softening composition containing as its essential lubricating and softening agent a derivative of phosphorus having the general formula:
- a is a substituent selected from the group consisting of oxygen and sulfur; R is an alkoxyalkyl group, B is a substituent selected from the JOSEPH B. DICKEY. JAMES B. NORMINGTON.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Patented 20, 1942.
YARN OONDITIONING PROCESS AND COM- POSITION THEREFOR Joseph B. Dickey and' James B. Normington, Rochester, N. Y., assignors to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey No Drawing. Application December 17, 1938', Serial No. 246,512
17 Claims.
This invention relates to the conditioning of textile yarns and more particularly to the conditioning of filaments and yarns composed of organic derivatives of cellulose such as cellulose acetate, cellulose propionate, cellulose acetate propionate, and cellulose acetate butyrate, to render them more amenable to textile operations such as knitting and the like.
As is well known in the manufacture of yarns, particularly those composed of or containing cellulose organic derivatives, it is necessary to treat the yarn in order to reduce the tendency toward breakage of the individual filaments or fibers when they are subjected to various mechanical strains and to lubricate the yarn in order to facilitate handling in such operations as spinning, twisting, winding, and reeling. It is also necessary to treat yarn to adapt it for use as warp or filling orfor the manufacture of various types of knitted fabrics. In knitting, it is particularly important that the yarn be soft and piable in order that it may conform readily to the contour of the needles and thus produce a closely knit fabric free from such defects as stitch distortion, pin holes, laddering, and the like.
Heretofore it has been proposed to employ softening agents such as polyhydric alcohols and similar agents as ingredients of yarn conditioning or lubricating formulas, generally in connection with mineral, animal or vegetable oils. It has been found, however, that most of the known softening agents and the various formulas containing them have certain drawbacks, one of the most serious of which is high vapor pressure, and in some cases too drastic a solvent action on theyarn. Many of such agents possess slight or insufficient solvent power for the lubricants with which they are used, and it s accordingly necessary to employ blending agents or emulsifying agents in order to obtain operable yarn treating formulas. In addition, many of the known softening and lubricating agents are insufficiently soluble in water to permit satisfactory removal by aqueous scour bathsi This invention has as its principal object to provide an entirely new class of yarn conditioning agents which are particularly adapted for the treatment of yarns composed of or containing organic derivatives of cellulose and capable of lubricating, softening and rendering such yarns more amenable to knitting and other textile operations. A further and specific object is to provide a class of conditioning agents which augment or assist the lubricating action of varand capable of employment in a variety of textile operations where complicated designs or stitches are employed. Another object is to provide an improved type of yarn which is especially amenable to textile operations including circular knitting, weaving, spinning and-the like.
Other objects will appear hereinafter.
These objects are accomplished by the following invention which, in its broader aspects, comprises the discovery that derivatives of phosphorus having the general formula:
where :c is a substituent selected from the group consisting of oxygen and sulfur; R is a substituent selected from the group consisting of alkyl and aryl groups, which groups may be substituted with other groups including alkoxy, polyalkoxy, tetrahydrofurfuryloxy, etc.: B is a substituent selected from the group consisting of and wherein B is a substituted amino group, OR, -0 alkyl, o-aryl and B, and wherein B is a substituted amino group, may be used as yarn conditioning agents and particularly as softening agents, with or without the addition of animal, mineral, or vegetable oils, in the treatment of yarns composed of or containing organic derivatives of cellulose. We have found that these compounds when employed as described in the detailed examples set forth below have a slight solvent and/or softening action on cellulose organic derivative yarns which renders such yarns soft and pliable without at the same time having too drastic an action thereon.
Examples of the preparation of typical compounds of this type are as follows:
PREPARATION OF COMPOUNDS Example 1 Di- (ethoxyethyl) -N,N-diethyl phosphonamide.
Diethylamino, di-(ethoxyethyl) phosphate.
(CzHs) 2N1|7=(O IHAO C2115) I Two equivalents of sodium are dissolved in an excess of ethoxyethanol and the solution cooled- Example 2 Di- (ethoxyethyl) phospho-piperidine.
One mole of piperidino-phosphoryl dichloride is added to two moles of potassium hydroxide dis solved in excess ethoxyethanol with agitation, at room temperature. The mixture is then heated on the steam bath for thirty minutes to complete the reaction, filtered and distilled.- B. P. 210-13/22 mm.
Example 3 Ethoxyethyl-N,N,N',N',-tetraethyl diamide.
phosphor- To one equivalent of ethoxyethyl phosphoryl dichloride dissolved in 100 cc. ether are added four equivalents of diethylamine in 200 cc. ether,
with stirring at l0-15. To complete the reaction, the mixture is refluxed for thirty minutes. l'he salt is then filtered out, and the filtrate distilled to obtain the desired product. B. P. 170-80/15 mm.
In accordance with the invention these compounds may be applied directly to the yarn during or after spinning, or may be added to the spinning solution itself. We have found that these compounds have exceptional solvent powers which enable them to dissolve mineral oils and blown and unblown, drying and semi-drying, vegetable and animal oils and accordingly they may be, and preferably are, employed as ingredients of yarn conditioning or lubricating formulas in conjunction with agents which function wholly. or partially as lubricants.
In the following examples and description we have set forth several of the preferred embodiments of our invention, but they are included merely for purposes of illustration and not as a limitation thereof.
Our invention will be more readily understood by reference to the following examples in which typical applications of the invention are set forth.
and applied to textile materials suchas silk, wool, cellulose acetate, viscose, etc. as descrimd above. It the yarn is intended for knitting primarily, the amount of conditioningliquid applied may vary from e25% by weight of the yarn, and if the yarn is intended for weaving, the amount of liquid applied may vary from 1-5% by weight of the yarn.
Example 4 A conditioning liquid is made up as follows:
CHr-O CzHuO Parts I l|[|NC4Ho 20 CHr-OCaIhO o Olive nil 80 Cellulose acetate filaments or fibers treated Example 5 Parts C2H5O CIHAO C2H40 P-N 25 C2115 Blown olive oil 75 Example 6 (HIP-CH1 CHz-CH CH2 Parts (C2H5-O CzH-1OC2H40)2=1|lT-N\ O 20 Light mineral oil Example 7 H Parts OC2H4O fi N-C:H4O C1Hi"0 CzH5 20 S OCaHs Neats-loot oil 80 Example 8 I Parts CmHzn- -O P-0 CzHr-O CH: 20
S N-CrHr /O CIHA S rm oil 60 1.2 mi 20 Example 9 CHz-?Hz P: OC2Hi0CsH4OCHz-$H CH2 II Parts 0 O 2 C4Hn N CAHD Tetrahydrofurfuryl alcohol 20 Blown soya been oil 60 Example 10 Parts Water 80 (Octal-0cm 10 l (L N-CHz-CH:
H: C i
CH5 Water soluble cellulose ester 5 Tetraethylene glycol 5 Example 11 A 20% solution of cellulose acetate in acetone in which is incorporated 1-25% by weight of the cellulose acetate of OCiH:
is extruded through fine orifices into an evaporative atmosphere.
The filaments thus pro- 1 duced are wound, or-twlsted and wound. Yarns produced from filaments, thus prepared are pliable and suitable for knitting.
Any of the above compositions may be applied to the yarn intended for use in circular knitting by means of a bath, wick, spray, roller, pad or any suitable means. The amount of conditioning liquid applied may vary between 5-25% by weight of the yarn. Usually, however, the
amount of conditioning liquid applied is about 10-15% by weight of the yarn. Yarn composed of cellulose acetate conditioned as described above gives excellent results when used in the circular knitting process,
As will be apparent from the above examples and description the conditioning agents of our invention may be applied by a wide variety of methods. For example, we may employ the agent as an ingredient of the spinning dope from which the filaments are formed, the amount of the agent 50 employed depending upon a number of factors, such as the particular cellulose derivative used in making the yarn, th'e solvent or solvent combination used in making up the spinning solution, and the degree of softness or pliability desired in the yarn,etc.
If the conditioning agent is to be applied to theyarn after spinning, this may be done by bringing the yarn in contact with a wick, roll, or felt wet therewith, or the liquid may be applied by immersion, spray, or otherwise. The particular point at which the liquid is applied may vary. It may, for example, be applied to the yarn inside or outsidecthe spinning cabinet, between the guide and godet roll, between the godet or other roll or guide and the point of winding and/or twisting. In some cases, the liquid may even be applied to the yarn after winding onto cones, spools, bobbins, or the like or by the socalled bobbin to bobbin method. In the case of staple fiber manufacture, the liquid may be applied to the yarn prior to, or after cutting into staple lengths.
The amount of the agent so employed will vary widely depending upon the results desired, the specific nature of the material to which the agent is applied, the use to which the yarn is eventually to be put and other factors. For example, in a given case where a cellulose organic acid ester yarn such as a yarn composed of cellulose acetate, is intended for knitting, about 4 to 25% or more by weight, based on the weight of the dry yarn, may be satisfactory, while if the yarn is intended for weaving, the amount may vary between about 1 and 5%.
Although in the above examples we have referred primarily to yarn treating compositions containing only the conditioning agent and an oil, other ingredients such as solvents, non-solvents, emulsifying agents, blending agents and the like, may be added within the scope of our invention. Likewise, various dyes or other coloring matter may be included in case it is desired to permanently or fugitively tint or dye the material undergoing treatment.
Although we have found it convenient to illustrate our invention by reference to compositions containing specific percentages of thevarious ingredients, these percentages may vary widely depending upon the particular purpose for which the composition is intended. For example, if it is desired to control the solvent or softening action of the conditioning agent, the amount of the agent may be adjusted as, for example, by reducing the amount of the agent and correspondingly increasing the amount of oil or other ingredient.
While we have described our invention with particular reference to the treatment of yarns composed of organic derivatives of cellulose such as cellulose acetate, the conditioning agents and formulas described herein are applicable to the conditioning of many other types of cellulose derivative yarns such as those composed of or containing cellulose propionate, cellulose butyrate, cellulose acetate propionate, cellulose acetate butyrate, ethyl cellulose, methyl cellulose, benzyl cellulose and others, as well as to the conditioning of silk, wool, cotton, viscose and other natural or artificial materials.
The term yarn as used herein and in the claims is to be understood as including a single filament, a plurality of filaments associated into the form of a thread, either of high or low twist,
single or multiple threads associated or twisted together, composite threads composed of a mixture of natural and artificial filaments or a composite thread formed by twisting together individual strands of natural or artificial materials, as well as cut staple fibers produced from natural and/or artificial filaments or threads and spun yarn produced from such stable fibers.
As indicated above, the yarn conditioning agents of our invention are exceptionally good solvents for a wide variety of mineral, blown and unblown, drying and semi-drying animal and vegetable oils such as cottonseed, olive, castor, neats-foot, sperm and other oils. This enables them to be used with any of such oils in making up a variety of yarn treating formulas of varying composition.
The yam conditioning method and compositions of our invention possess many outstanding advantages. The fundamental and outstanding characteristic of the agents employed in accordance with the invention is their ability to soften yarns, especially those composed of or containing organic derivatives of cellulose such as cellulose acetate and render them soft and pliable and amenable to various textile operations, especially operations such'as those involved in weaving and knitting where complicated designs or stitches are employed, without too drastic an action on the yarn material. Another outstanding characteristic of these compounds is their exceptional solvent power for a wide variety of mineral, animal, and. vegetable oils and their ability to act as lubricating assistants inconjunction with these oils when applied to such yarns. In addition, due to their solubility in water, they may be readily removed from yarns and fabrics by means of the usual aqueous scour baths. By employing the yarn'conditioning agents and method of our invention as herein described, one is enabled to obtain highly satisfactory results in the manufacture of yarns and woven fabrics and especially the production from these yarns of closely knit fabrics free from defects such as pin holes, stitch distortion, laddering and the like.
What we claim and desire to secure by Letters Patent of the United States is:
1. The process of conditioning yarn to render it more amenable to textile operations including knitting, weaving, spinning and the like, which comprises applying thereto a lubricating and softening composition containing as its essentiallubricating and softening component a derivative of phosphorus having the general formula:
where a: is a substituent selected from the group consisting of oxygen and sulfur; R is an alkoxy alkyl group, B is a substituent selected from the group consisting of OR, -o-alkyl, -o-aryl and B; and B is a substituted amino group.
2. The process of conditioning yarn composed of or containing organic derivatives of cellulose to render it more amenable to textile operations including knitting, weaving, spinning and the like, which comprises applying thereto a lubricating and softening composition containing as its essential lubricating and softening component a derivative of phosphorus having the general formula:
where a is a substituent selected from the group consisting of oxygen and sulfur; R is an alkoxyalkyl group, 33 is a substituent selected from the group consisting of OR, -o-alkyl, -o-aryl and B; and B is a substituted amino group.
3. The process of conditioning yarn composed of or containing cellulose acetate to render it more amenable to textile operations including knitting, weaving, spinning, and the like, which comprises applying thereto a lubricating and softening compositoin containing as its essential lubricating and softening component aderivative of phosphorus having the general formula:
where s: is a substituent selected from the group consisting of oxygen and sulfur; R is an alkoxy: alkyl group, B is a substituent selected from. the group consisting of OR, -o-alkyl, -o-aryl and B; and B is a substituted amino group.
4. The process of conditioning yarn composed of or containing cellulose acetate to render it more amenable to textile operations including knitting, weaving, spinning, and the like, which comprises applying thereto a lubricating and softening composition containing as its essential lubricating and softening component a derivative of phosphorus having the general formula:
decyl ester of di-p-methoxy ethyl phosphamate.
6. The process of conditioning yarn composed of or containing cellulose acetate to render it more amenable to textile operations including knitting, weaving, spinning, and the like which comprises applying thereto alubricating and softening composition containing as its essential lubricating and softening component di-pme hoxy ethyl ester of monobutyl phosphamate.
'7. The process of conditioning yarn composed of or containing cellulose acetate to render it more amenable to textile operations including knitting, weaving, spinning, and the like which comprises applying thereto a lubricating and" softening composition containing as its essential lubricating and softening component p'-ethoxyp-ethoxyethyl-methyl ester 9f thio diethyl phosphamic acid.
8. Textile yarns amenable to textile operations including knitting,- weaving, spinning, and the like, impregnated with a lubricating and softening composition containing as its essential lubricating and softening component a derivative of phosphorus having the general formula:
where a: is a substituent selected from the group consisting of oxygen and sulfur; R is an alkoxyalkyl group, B is a substituent selected from the group consisting of OR, -o-alkyl, -o-ary1 and B; and B is a substituted amino group,
9. Textile yarns composed of or containing organic derivatives of cellulose amenable to textile operations including knitting, weaving, spinning, and the like impregnated with a lubricating and softening composition containing as its essential lubricating and softening component a derivative of phosphorus having the general formula:
. z where a: is a substituent selected from the group consisting of oxygen and sulfur; R, is an alkoxyalkyl group, B is a substituent selected from the group consisting of OR, -o-alkyl, -o-aryl and B; and B is a substituted amino group.
10. Textile yarns composed of orcontaining cellulose acetate amenable to textile operations including knitting, weaving, spinning, and the like impregnated with a lubricating and softening composition containing as its essential lubricating and softening component a derivative of phosphorus having the general formula:
where a: is a substituent selected from the group consisting of oxygen and sulfur; R is an alkoxyalkyl group, B is a substituent selected from the group consisting of OR, o-alkyl, -o-aryl and B; and B is a substituted amino group.
11. Textile yarns composed of or containing cellulose aceate amenable to-textile operations including knitting, weaving, spinning, and the like, impregnated with a lubricant comprising dioctadecyl ester of di-B-methoxyethyl phosphamate.
12. Textile yarns composed of or containing cellulose acetate amenable' to textile operations including knitting, weaving, spinning, and the like, impregnated with a lubricant pomprising di-p-methoxy ethyl ester of monobutyl phosphamate.
13. Textile yarns composed of or containing cellulose acetate amenable to textile operations including knitting, weaving, spinning, and the like, impregnated with a. lubricant comprising p-ethoxy-fl-ethoxyethyl-methyl ester of thio diethyi phosphamic acid.
14. A textile yarn lubricating and softening composition containing as its essential lubricating and softening agent a derivative of phosphorus having the general formula:
where a: is a substituent selected from the group consisting of oxygen and sulfur; R is an alkoxyalkyl group, B is a substituent selected from the JOSEPH B. DICKEY. JAMES B. NORMINGTON.
l5 acid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US246512A US2299535A (en) | 1938-12-17 | 1938-12-17 | Yarn conditioning process and composition therefor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US246512A US2299535A (en) | 1938-12-17 | 1938-12-17 | Yarn conditioning process and composition therefor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2299535A true US2299535A (en) | 1942-10-20 |
Family
ID=22930990
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US246512A Expired - Lifetime US2299535A (en) | 1938-12-17 | 1938-12-17 | Yarn conditioning process and composition therefor |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2299535A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2552539A (en) * | 1949-04-15 | 1951-05-15 | Dow Chemical Co | Diamidothiophosphates |
| US2552540A (en) * | 1949-04-15 | 1951-05-15 | Dow Chemical Co | O-methoxy o-alkyl amidothiophosphates |
| US2648706A (en) * | 1950-09-29 | 1953-08-11 | California Research Corp | Amides of alkane phosphonic acids |
| US3159645A (en) * | 1960-12-29 | 1964-12-01 | Dow Chemical Co | Omcrion-thiazolyl omcrion-alkyl phosphoramido-thioates |
| US3428481A (en) * | 1966-07-06 | 1969-02-18 | Du Pont | Antistatic lubricating composition for textile fibers |
| US4556710A (en) * | 1983-03-18 | 1985-12-03 | The Dow Chemical Company | Primary hydroxyl-containing phosphono-s-triazines |
-
1938
- 1938-12-17 US US246512A patent/US2299535A/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2552539A (en) * | 1949-04-15 | 1951-05-15 | Dow Chemical Co | Diamidothiophosphates |
| US2552540A (en) * | 1949-04-15 | 1951-05-15 | Dow Chemical Co | O-methoxy o-alkyl amidothiophosphates |
| US2648706A (en) * | 1950-09-29 | 1953-08-11 | California Research Corp | Amides of alkane phosphonic acids |
| US3159645A (en) * | 1960-12-29 | 1964-12-01 | Dow Chemical Co | Omcrion-thiazolyl omcrion-alkyl phosphoramido-thioates |
| US3428481A (en) * | 1966-07-06 | 1969-02-18 | Du Pont | Antistatic lubricating composition for textile fibers |
| US4556710A (en) * | 1983-03-18 | 1985-12-03 | The Dow Chemical Company | Primary hydroxyl-containing phosphono-s-triazines |
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