US2498408A - Antistatic textile materials - Google Patents
Antistatic textile materials Download PDFInfo
- Publication number
- US2498408A US2498408A US633266A US63326645A US2498408A US 2498408 A US2498408 A US 2498408A US 633266 A US633266 A US 633266A US 63326645 A US63326645 A US 63326645A US 2498408 A US2498408 A US 2498408A
- Authority
- US
- United States
- Prior art keywords
- textile
- phosphate
- yarns
- static
- ethyl acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004753 textile Substances 0.000 title claims description 71
- 239000000463 material Substances 0.000 title claims description 58
- 239000002253 acid Substances 0.000 claims description 48
- 229910019142 PO4 Inorganic materials 0.000 claims description 47
- 239000010452 phosphate Substances 0.000 claims description 46
- 238000009825 accumulation Methods 0.000 claims description 15
- 239000010687 lubricating oil Substances 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- NLAYVTPUNIVXFK-FDDDBJFASA-N [(2r,3s,4r,5r)-3,4-dihydroxy-5-[5-(methylaminomethyl)-2,4-dioxopyrimidin-1-yl]oxolan-2-yl]methyl dihydrogen phosphate Chemical compound O=C1NC(=O)C(CNC)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(O)=O)O1 NLAYVTPUNIVXFK-FDDDBJFASA-N 0.000 claims 1
- -1 lauryl ethyl Chemical group 0.000 description 44
- 239000000835 fiber Substances 0.000 description 24
- 239000002216 antistatic agent Substances 0.000 description 16
- 229920002678 cellulose Polymers 0.000 description 15
- 239000001913 cellulose Substances 0.000 description 13
- 239000004744 fabric Substances 0.000 description 13
- 230000003068 static effect Effects 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 229920002301 cellulose acetate Polymers 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 230000005611 electricity Effects 0.000 description 6
- 238000009987 spinning Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000019198 oils Nutrition 0.000 description 5
- 239000000314 lubricant Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000004006 olive oil Substances 0.000 description 4
- 235000008390 olive oil Nutrition 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- 238000009941 weaving Methods 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000009940 knitting Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 229920002955 Art silk Polymers 0.000 description 1
- 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 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 235000004879 dioscorea Nutrition 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229940059904 light mineral oil Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding 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
- 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
-
- 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
- D06M13/10—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 oxygen
- D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/402—Castor oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/46—Textile oils
-
- 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
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/15—Antistatic agents not otherwise provided for
- Y10S260/16—Antistatic agents containing a metal, silicon, boron or phosphorus
-
- 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
- Y10T428/31—Surface property or characteristic of web, sheet or block
-
- 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
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2418—Coating or impregnation increases electrical conductivity or anti-static quality
- Y10T442/2451—Phosphorus containing
-
- 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
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2861—Coated or impregnated synthetic organic fiber fabric
- Y10T442/2869—Coated or impregnated regenerated cellulose fiber fabric
Definitions
- the present invention relates to the treatment of textile materials such as fibers, yarns, filaments, threads, and the like to render such materials anti-static so that they will not generate or accumulate electrical charges during the performance of textile operations thereon, such as, twisting, winding, warping, carding, combing, drawing, spinning, weaving, knitting, and the like.
- the invention also relates, in particular, to the treatment of cellulose organic derivative textile materials as, for instance, fibers, yarns, threads, filaments, fabrics and the like of cellulose acetate, to reduce or eliminate their tendency to generate or accumulate charges of electricity due to frictional forces that they may encounter during the performance of textile operations, or in use as wearing apparel.
- cellulose organic derivative textile materials as, for instance, fibers, yarns, threads, filaments, fabrics and the like of cellulose acetate
- cellulose derivative fibers filaments or yarns. Being smoothlike in their structure and also of the low moisture content compared to natural fibers. such as. cotton and wool, cellulose derivative yarns are inherently more susceptible to accumulation of static. Often the charges accumulated are so great as to cause considerable separation of the individual fibers with the result that it is difiicult to form compact yarns or slivers.
- lauryl ethyl acid o-phosphate by treating or incorporating into textile materials lauryl ethyl acid o-phosphate, that such treated textile materials are free from the tendency to accumulate electrical charges and may be subjected to textile operations without encountering this difilculty.
- lauryl ethyl acid o-phosphate involves many advantages.
- the textile materials treated with this agent in addition to readily dissipating any electrical charges that may tend to form, remain non-tacky, non-gummy, and can be readily manipulated during the textile operations.
- lauryl ethyl acid o-phosphate is non-corrosive to the machinery upon which the textile operations are performed, is highly stable to oxidizing influences, does not age, and may be readily removed, when desired, from the textile material by simple scouring operations after the textile operations have been performed.
- this compound is highly compatible with emulsifying, softening, or lubricating agents and may be readily applied to the textile yarns with or without such agents. Another particular advantage of this compound is that it readily wets the textile materials, and thus spreads over the materials quickly and thoroughly.
- this compound may be applied to already formed fabrics.
- the fabric does not retain charges of static electricity.
- womens wearing apparel prepared from artificial silk, such as cellulose acetate, particularly when worn as an outer garment over a silk or wool under garment accumulates charges of electricity during use and tends to adhere or cling to the 'wearers body, thus affecting adversely the lines and designs of the garment.
- Fabrics treated according to my invention or prepared from yarns so treated do not accumulate electrical charges and accordingly do not tend to cling to the wearer's body but hang freely thereon.
- the fabric so treated with the anti-static agent of my invention is not of! odor and is free from any tacky or gummy feeling. Since they are not tacky and do not become charged with electricity, another advantage of "such treated fabrics is that dust particles which normally are attracted by static charges do not cling readily to such materials and may be readily removed by brushing or shaking.
- Another object of my invention is to provide a method of overcoming the difliculties attendant the handling and manipulation of textile fibers and yarns involved in the conversion of such materials into textile fabrics.
- a further object of the invention is to provide textile materials which are free from the tendency to accumulate or generate electrical charges.
- a still further object is to provide a composition which when applied to textile yarns, filaments, or fibers eliminates the tendency of such materials to accumulate static charges.
- the above and other objects of my invention are accomplished by treating or incorporating into fibers, yarns, threads, filaments, or fabrics, a small amount of lauryl ethyl acid o-phosphate.
- the textile materials treated according to my invention may be .composed of any of the wellknown textile materials, such as, cotton, wool, silk, flax, artificial yarns, as for example, yarns prepared from regenerated cellulose of the viscose or cuprammonium type, nylon, or from proteins as casein.
- my invention finds its greatest effectiveness and most effective application in the treatment of yarns, filaments, fibers or threads, formed from organic derivatives of cellulose which are normally either non-conductors or weak conductors of electricity, as for example, cellulose esters and ethers of cellulose. More specifically, as examples of such organic esters of cellulose, there may be mentioned cellulose acetate, cellulose formate, cellulose propionate, cellulose butyrate. As examples of organic ethers of cellulose, there may be mentioned the ethyl-, methyl-, or butyl-cellulose.
- lauryl ethyl acid o-phosphate is prefer-ably applied to the yarns, filaments, fibers or threads and the like, after they have been formed, it is to be understood that this antistatic agent may be incorporated in the solution of the organic derivative of cellulose from which such artificial products are spun.
- this antistatic agent may be incorporated in the solution of the organic derivative of cellulose from which such artificial products are spun.
- larger amounts of the lauryl ethyl acid o-phosphate may be applied.
- lauryl ethyl acid phosphate is effective when it is applied to the textile materials together with a lubricant such as mineral, vegetable or animal oil as, for instance, a light mineral oil, olive oil, sperm oil, blown olive oil or blown sperm oil, or other suitable lubricating oils, such as, for example, sulfonated castor oil.
- a lubricant such as mineral, vegetable or animal oil as, for instance, a light mineral oil, olive oil, sperm oil, blown olive oil or blown sperm oil, or other suitable lubricating oils, such as, for example, sulfonated castor oil.
- the lauryl ethyl acid o-phosphate or similar anti-static agent according to the invention is applied in conjunction with a textile lubricating oil of the type exemplified above, in an amount such that about 99 to about 90 parts of the textile lubricating oil are mixed with from about 1 to about 10 parts of the lauryl ethyl acid o-phosphate or similar agent.
- the amount of lauryl ethyl acid o-phosphate or similar agent should be such that when the mixture is applied to the textile material, from about 0.1% to about 10%, based on the weight of the treated material, is applied thereto, such quantity being sufficient to prevent the accumulation of electrical charges in the textile material.
- the lauryl ethyl acid o-phosphate alone or with a lubricant may be applied in any suitable manner as by immersion, spraying, roller, wick or felt.
- the anti-static agent may be applied by passing the yarns over wicks or felt bodies dipping into the anti-static material.
- the anti-static material is preferably applied after dyeing. This may readily be carried out by passing the fabric over rollers dipping into a trough containing the lauryl ethyl acid o-phosphate or a solution or suspension thereof.
- the anti-static agent may be applied in compositions containing such lubricants. If desired, the antistatic agent may also be applied in the form of ples are merely by Way of illustration and are not to be considered as limiting the invention.
- Example 1 Cellulose acetate yarns, as they leave the spinning cabinet, are made to pass over wicks or rollers to which there is supplied lauryl ethyl acid o-phosph ate.
- the rate of application is such that about 0.3% of lauryl ethyl acid o-phosphate, based on the weight of the treated material, is applied to the yarn.
- Example 2 A yarn of cellulose acetate, as it is drawn from I the spinning cabinet is caused to pass across a Example 3
- Yarns prepared from cellulose acetate are treated with an emulsion containing parts of lauryl ethyl acid o-phosphate, 900 parts of olive oil and 10,000 parts of water so that the amount of emulsion applied is about 4%, based on the weight of the treated yams.
- the yarns may then cases be readily converted into staple fibers, and the resulting fibers spun into yarn without encountering any difficulties due to accumulation or electrical charges, since such treated fibers bleed off" any charges formed during the yarn forming operation.
- Example 4 To cotton yarns, there is applied a solution comprising 30 parts of mineral oil, 65 parts of olive oil and 5 parts of lauryl ethyl acid ophosphate. The solution is applied to the yarn at such a rate that about 0.5% of the anti-static agent, based on the weight of the finished yarn, is incorporated therein. In the weaving of such a treated yarn, static electrical charges are completelyeliminatcd.
- Example 5 To a solution of cellulose acetate in acetone such as is conventionally utilized in the spinning of textile fibers, there is added about 2%% of lauryl ethyl acid o-phosphate, based on the weight of the cellulose acetate. This solution is then extruded into an atmosphere wherein the acetone is evaporated from the solution.
- the filaments thus produced are readily wound or twisted without the formation of any static electrical charges.
- the filaments so prepared may be readily cut to form staple fibers and such fibers may be readily formed into yarns without encountering any difficulties due to the generation of static.
- Example 6 To a 25% solution of cellulose acetate in acetone, there is added 5% of lauryl ethyl acid 0- phosphate based on the weight of cellulose acetate. The resulting solution may then be spun into filaments by any suitable method of spinning such as the wet or dry method. a The filaments thus obtained may be twisted into yarn or cut into staple fibers which may then be spun into .yarns without encountering any accumulation of electrical charges.
- the lauryl ethyl acid o-phosphate may be employed alone or with a textile treating agent as an oil, as pointed out above.
- a textile treating agent as an oil
- other agents may be applied to the textile material simultaneously with the anti-static agent, such as, emulsifying agents, blending agents, dyes or other coloring matter where it is desired to color the material while it is undergoing the anti-static treatment.
- emulsifying agents such as, emulsifying agents, blending agents, dyes or other coloring matter where it is desired to color the material while it is undergoing the anti-static treatment.
- dyes or other coloring matter where it is desired to color the material while it is undergoing the anti-static treatment.
- the specific examples pertain to specific percentages of the various ingredients of the compositions. that the proportions may be varied within relatively wide limits depending upon the nature of the textile fiber treated.
- the lauryl ethyl acid o-phosphate possesses outstanding antistatic activity. and particularly in connection with textile materials comprising organic derivatives of cellulose. It is easily applied and because of its ready spreading action, and solubility in oils, it also renders the textile materials amenable to the various textile operations. Its properties, chemical stability, and stability against oxidation and the ease with which it may be readily removed from the textile materials when it is no longer required add to its outstanding characteristics as an anti-static agent.
- lauryl ethyl acid o-phosphate While the greatest advantages are obtained with lauryl ethyl acid o-phosphate, and this is the preferred embodiment of my invention, other compounds of a similar nature in which the lauryl group is replaced by an alkyl group of from 6 to and including 18 carbon atoms may be employed. Also, the ethyl group may be replaced by a methyl, propyl, isopropyl or butyl group. In general, dialkyl acid o-phosphates may be employed in which one of the alkyl groups contains from 6 to 18 carbon atoms and the other from 1 to 4 carbon atoms.
- lauryl methyl acid 0- phosphate lauryl propyl acid o-phosphate
- lauryl isopropyl acid o-phosphate lauryl butyl acid 0- phosphate, hexyl ethyl acid o-phosphate, stearyl ethyl acid o-phosphate, undecyl propyl acid 0- phosphate, octyl butyl acid o-phosphate, and other combinations of the long chain and short chain alkyl groups.
- lauryl ethyl acido-phosphate constitutes the preferred embodiment of my invention.
- Textile material containing from about 99 to about parts of a textile lubricating oil and from about 1 to about 10 parts of a dialkyl acid 0- phosphate wherein one of the alkyl groups'has from 6 to 18 carbon atoms and the other from 1 to 4 carbon atoms, the quantity of dialkyl acid o-phosphate present ranging from about 0.1% to about 10%, based on the weight of the treated material, so as to be suflicient to prevent the accumulation of electrical charges in said textile material.
- Textile material containing from about 99 to about 90 parts of a textile lubricating oil and from about 1 to about 10 parts of lauryl ethyl acid o-phosphate, the quantity of lauryl ethyl acid o-phosphate present ranging from about 0.1% to about 10%, based on the weight of the treated material, so as to be sufficient to prevent the accumulation of electrical charges in said textile material.
- Textile material containing from about 99 to about 90 parts of a textile lubricating oil and from about 1 to about 10 parts of hexyl ethyl acid o-phosphate, the quantity of hexyl ethyl acid o-phosphate' present ranging from about 0.1% to about 10%, based on the weight of the treated material, so as to be sufficient to prevent the accumulation of electrical charges in said textile material.
- Textile material containing from about 99 to about 90 parts of a textile lubricating oil and from about 1 to about 10 parts of stearyl ethyl acid o-phosphate, the quantity of stearyl ethyl acid o-phosphate present ranging from about 0.1% to about 10%, based on the weight of the treated material, so as to be sufficient to prevent the accumulation of electrical charges in said textile material.
- Textile material containing in amount suincient to prevent the accumulation of electrical charges in said textile materials a dialkyl acid o-phosphate wherein one of the alkyl groups has from 6 to 18 carbon atoms and the other from 1 to 4 carbon atoms.
- a cellulose ester textile material contain- UNITED STATES PATENTS ing in amount suflicient to prevent the accumula-- N ber Name Date tion of electrical charges in said textile materials 1,914,331 Nuesslein et al June 13, 1933 a, dialkyl acid o-phosphate wherein one of the 2,005,619 Graves June 18, 1935 alkyl groups has from 6 to 18 carbon atoms and 10 2,080,299 Bennlng et'al. May 11, 1937 the other from 1 to 4 carbon atoms. 2,345,734 Dickey et a1. Apr. 4, 1944 ARTHUR L. FOX.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Patented Feb. 21, 1950 AN TISTATIC TEXTILE MATERIALS Arthur L. Fox, Easton, Pa., assignor to General Aniline & Film Corporation, New York, N. Y., a corporation of Delaware No Drawing. Application December 6, 1945, Serial No. 633,266
7 Claims.
The present invention relates to the treatment of textile materials such as fibers, yarns, filaments, threads, and the like to render such materials anti-static so that they will not generate or accumulate electrical charges during the performance of textile operations thereon, such as, twisting, winding, warping, carding, combing, drawing, spinning, weaving, knitting, and the like.
The invention also relates, in particular, to the treatment of cellulose organic derivative textile materials as, for instance, fibers, yarns, threads, filaments, fabrics and the like of cellulose acetate, to reduce or eliminate their tendency to generate or accumulate charges of electricity due to frictional forces that they may encounter during the performance of textile operations, or in use as wearing apparel.
In the performance of textile operations on textile materials in the form of filaments, yarns, threads or staple fibers, considerable difficulty is experienced because the yarns acquire an electrical charge due to the frictional and other infiuences encountered in the textile operations. The electrical charge causes the yarns and fibers to fly around in an unmanageable manner so that the formation of the yarn or of the fabric is rendered quite difficult. Particularly, in the utilization of staple fibers, the static electrical char es produced are often so great as to prevent the fibers from adhering to each other and thereby cause considerable difficulty in the spinning operation. In the case of knitting or weaving, the accumulation of static charges interferes with the smooth formation of the web or textile fabric.
The accumulation of electrical charges is particularly a problem in the case of carrying out textile operations on cellulose derivative fibers. filaments or yarns. Being smoothlike in their structure and also of the low moisture content compared to natural fibers. such as. cotton and wool, cellulose derivative yarns are inherently more susceptible to accumulation of static. Often the charges accumulated are so great as to cause considerable separation of the individual fibers with the result that it is difiicult to form compact yarns or slivers.
Considerable effort has been devoted by workers in the textile field to develop suitable anti staticagents that would prevent or eliminate the accumulation of electrical charges on textile materials. Various agents and compositions for this purpose have already been proposed.
I have discovered that by treating or incorporating into textile materials lauryl ethyl acid o-phosphate, that such treated textile materials are free from the tendency to accumulate electrical charges and may be subjected to textile operations without encountering this difilculty. The employment of lauryl ethyl acid o-phosphate involves many advantages. The textile materials treated with this agent, in addition to readily dissipating any electrical charges that may tend to form, remain non-tacky, non-gummy, and can be readily manipulated during the textile operations. In addition, lauryl ethyl acid o-phosphate is non-corrosive to the machinery upon which the textile operations are performed, is highly stable to oxidizing influences, does not age, and may be readily removed, when desired, from the textile material by simple scouring operations after the textile operations have been performed. Furthermore, this compound is highly compatible with emulsifying, softening, or lubricating agents and may be readily applied to the textile yarns with or without such agents. Another particular advantage of this compound is that it readily wets the textile materials, and thus spreads over the materials quickly and thoroughly.
Instead of applying the lauryl ethyl acid 0- phoshate to fibers, yarns, or filaments, this compound may be applied to already formed fabrics. In this case, and in the case of fabrics which have been made from yarns treated with this antistatic agent, the fabric does not retain charges of static electricity. As is well known, womens wearing apparel prepared from artificial silk, such as cellulose acetate, particularly when worn as an outer garment over a silk or wool under garment, accumulates charges of electricity during use and tends to adhere or cling to the 'wearers body, thus affecting adversely the lines and designs of the garment. Fabrics treated according to my invention or prepared from yarns so treated do not accumulate electrical charges and accordingly do not tend to cling to the wearer's body but hang freely thereon.
In addition, the fabric so treated with the anti-static agent of my invention is not of! odor and is free from any tacky or gummy feeling. Since they are not tacky and do not become charged with electricity, another advantage of "such treated fabrics is that dust particles which normally are attracted by static charges do not cling readily to such materials and may be readily removed by brushing or shaking.
From the above considerations, it will be seen that the use of lauryl ethyl acid o-phosphate when applied to or incorporated into textile materials and particularly into cellulose derivative textile'materials, results in many advantageous efiects.
It is a principal object of my invention to render textile materials free from the tendency to accumulate static electrical charges.
It is a further object of my invention to treat cellulose derivative yarns, fibers, or filaments to reduce or eliminate the tendency of such textile materials to generate or accumulate static electrical charges due to frictional influences.
Another object of my invention is to provide a method of overcoming the difliculties attendant the handling and manipulation of textile fibers and yarns involved in the conversion of such materials into textile fabrics.
A further object of the invention is to provide textile materials which are free from the tendency to accumulate or generate electrical charges.
A still further object is to provide a composition which when applied to textile yarns, filaments, or fibers eliminates the tendency of such materials to accumulate static charges. 1
The above and other objects of my invention are accomplished by treating or incorporating into fibers, yarns, threads, filaments, or fabrics, a small amount of lauryl ethyl acid o-phosphate. The textile materials treated according to my invention may be .composed of any of the wellknown textile materials, such as, cotton, wool, silk, flax, artificial yarns, as for example, yarns prepared from regenerated cellulose of the viscose or cuprammonium type, nylon, or from proteins as casein. However, my invention finds its greatest effectiveness and most effective application in the treatment of yarns, filaments, fibers or threads, formed from organic derivatives of cellulose which are normally either non-conductors or weak conductors of electricity, as for example, cellulose esters and ethers of cellulose. More specifically, as examples of such organic esters of cellulose, there may be mentioned cellulose acetate, cellulose formate, cellulose propionate, cellulose butyrate. As examples of organic ethers of cellulose, there may be mentioned the ethyl-, methyl-, or butyl-cellulose.
While the lauryl ethyl acid o-phosphate is prefer-ably applied to the yarns, filaments, fibers or threads and the like, after they have been formed, it is to be understood that this antistatic agent may be incorporated in the solution of the organic derivative of cellulose from which such artificial products are spun. I have found that it is necessary to use only small amounts of the lauryl ethyl acid o-phosphate in order to render the textile materials completely effective to prevent the generation or accumulation of static electricity, for example, as little as 0.3%, based on the weight of the treated material will render the material completely effective in anti-static properties. However, if it is desired, larger amounts of the lauryl ethyl acid o-phosphate may be applied. On the other hand, even smaller amounts, such as, 0.1% of the lauryl ethyl acid phosphate is effective when it is applied to the textile materials together with a lubricant such as mineral, vegetable or animal oil as, for instance, a light mineral oil, olive oil, sperm oil, blown olive oil or blown sperm oil, or other suitable lubricating oils, such as, for example, sulfonated castor oil.
According to the preferred embodiment of the invention, the lauryl ethyl acid o-phosphate or similar anti-static agent according to the invention, is applied in conjunction with a textile lubricating oil of the type exemplified above, in an amount such that about 99 to about 90 parts of the textile lubricating oil are mixed with from about 1 to about 10 parts of the lauryl ethyl acid o-phosphate or similar agent. The amount of lauryl ethyl acid o-phosphate or similar agent, should be such that when the mixture is applied to the textile material, from about 0.1% to about 10%, based on the weight of the treated material, is applied thereto, such quantity being sufficient to prevent the accumulation of electrical charges in the textile material. Somewhat larger quantitles of the anti-static agent according to the invention could be applied but are usually unnecessary because of the ease of spreading of the anti-static agent, particularly in admixture with the textile lubricating oil, and the high antistatic properties of the agents according to the present invention.
The lauryl ethyl acid o-phosphate alone or with a lubricant may be applied in any suitable manner as by immersion, spraying, roller, wick or felt. Thus, in the case of yarns, the anti-static agent may be applied by passing the yarns over wicks or felt bodies dipping into the anti-static material. In the treatment of fabrics prepared from yarns not treated with the anti-static material, the anti-static material is preferably applied after dyeing. This may readily be carried out by passing the fabric over rollers dipping into a trough containing the lauryl ethyl acid o-phosphate or a solution or suspension thereof.
Since the lauryl ethyl acid o-phosphate is readily soluble in animal, vegetable, or mineral oils as, for example, blown and unblown vegetable oils as olive, teaseed, castor, soy bean etc., the anti-static agent may be applied in compositions containing such lubricants. If desired, the antistatic agent may also be applied in the form of ples are merely by Way of illustration and are not to be considered as limiting the invention.
Example 1 Cellulose acetate yarns, as they leave the spinning cabinet, are made to pass over wicks or rollers to which there is supplied lauryl ethyl acid o-phosph ate. The rate of application is such that about 0.3% of lauryl ethyl acid o-phosphate, based on the weight of the treated material, is applied to the yarn.
Example 2 A yarn of cellulose acetate, as it is drawn from I the spinning cabinet is caused to pass across a Example 3 Yarns prepared from cellulose acetate are treated with an emulsion containing parts of lauryl ethyl acid o-phosphate, 900 parts of olive oil and 10,000 parts of water so that the amount of emulsion applied is about 4%, based on the weight of the treated yams. The yarns may then cases be readily converted into staple fibers, and the resulting fibers spun into yarn without encountering any difficulties due to accumulation or electrical charges, since such treated fibers bleed off" any charges formed during the yarn forming operation.
v Example 4 To cotton yarns, there is applied a solution comprising 30 parts of mineral oil, 65 parts of olive oil and 5 parts of lauryl ethyl acid ophosphate. The solution is applied to the yarn at such a rate that about 0.5% of the anti-static agent, based on the weight of the finished yarn, is incorporated therein. In the weaving of such a treated yarn, static electrical charges are completelyeliminatcd.
Example 5 To a solution of cellulose acetate in acetone such as is conventionally utilized in the spinning of textile fibers, there is added about 2%% of lauryl ethyl acid o-phosphate, based on the weight of the cellulose acetate. This solution is then extruded into an atmosphere wherein the acetone is evaporated from the solution. The filaments thus produced are readily wound or twisted without the formation of any static electrical charges. The filaments so prepared may be readily cut to form staple fibers and such fibers may be readily formed into yarns without encountering any difficulties due to the generation of static.
Example 6 To a 25% solution of cellulose acetate in acetone, there is added 5% of lauryl ethyl acid 0- phosphate based on the weight of cellulose acetate. The resulting solution may then be spun into filaments by any suitable method of spinning such as the wet or dry method. a The filaments thus obtained may be twisted into yarn or cut into staple fibers which may then be spun into .yarns without encountering any accumulation of electrical charges.
It is to be understood that the lauryl ethyl acid o-phosphate may be employed alone or with a textile treating agent as an oil, as pointed out above. However, in addition to oils, other agents may be applied to the textile material simultaneously with the anti-static agent, such as, emulsifying agents, blending agents, dyes or other coloring matter where it is desired to color the material while it is undergoing the anti-static treatment. It is further to be understood that while the specific examples pertain to specific percentages of the various ingredients of the compositions. that the proportions may be varied within relatively wide limits depending upon the nature of the textile fiber treated.
It will be seen that my method of preventing and eliminating static charges and the anti-stat c agent utilized possesses many outstanding advantages. In the first place, the lauryl ethyl acid o-phosphate possesses outstanding antistatic activity. and particularly in connection with textile materials comprising organic derivatives of cellulose. It is easily applied and because of its ready spreading action, and solubility in oils, it also renders the textile materials amenable to the various textile operations. Its properties, chemical stability, and stability against oxidation and the ease with which it may be readily removed from the textile materials when it is no longer required add to its outstanding characteristics as an anti-static agent.
While the greatest advantages are obtained with lauryl ethyl acid o-phosphate, and this is the preferred embodiment of my invention, other compounds of a similar nature in which the lauryl group is replaced by an alkyl group of from 6 to and including 18 carbon atoms may be employed. Also, the ethyl group may be replaced by a methyl, propyl, isopropyl or butyl group. In general, dialkyl acid o-phosphates may be employed in which one of the alkyl groups contains from 6 to 18 carbon atoms and the other from 1 to 4 carbon atoms. As examples of such compounds may be mentioned, lauryl methyl acid 0- phosphate, lauryl propyl acid o-phosphate, lauryl isopropyl acid o-phosphate, lauryl butyl acid 0- phosphate, hexyl ethyl acid o-phosphate, stearyl ethyl acid o-phosphate, undecyl propyl acid 0- phosphate, octyl butyl acid o-phosphate, and other combinations of the long chain and short chain alkyl groups. As illustrative of the application of these compounds for rendering textile materials anti-static they may be employed in the same manner as the lauryl ethyl acid o-phosphate as illustrated in the hereinabove described examples. However, because of its outstanding antistatic activity and other highly advantageous properties hereinbefore mentioned, lauryl ethyl acido-phosphate constitutes the preferred embodiment of my invention.
I claim:
1. Textile material containing from about 99 to about parts of a textile lubricating oil and from about 1 to about 10 parts of a dialkyl acid 0- phosphate wherein one of the alkyl groups'has from 6 to 18 carbon atoms and the other from 1 to 4 carbon atoms, the quantity of dialkyl acid o-phosphate present ranging from about 0.1% to about 10%, based on the weight of the treated material, so as to be suflicient to prevent the accumulation of electrical charges in said textile material.
2. Textile material containing from about 99 to about 90 parts of a textile lubricating oil and from about 1 to about 10 parts of lauryl ethyl acid o-phosphate, the quantity of lauryl ethyl acid o-phosphate present ranging from about 0.1% to about 10%, based on the weight of the treated material, so as to be sufficient to prevent the accumulation of electrical charges in said textile material.
3. Textile material containing from about 99 to about 90 parts of a textile lubricating oil and from about 1 to about 10 parts of hexyl ethyl acid o-phosphate, the quantity of hexyl ethyl acid o-phosphate' present ranging from about 0.1% to about 10%, based on the weight of the treated material, so as to be sufficient to prevent the accumulation of electrical charges in said textile material.
4. Textile material containing from about 99 to about 90 parts of a textile lubricating oil and from about 1 to about 10 parts of stearyl ethyl acid o-phosphate, the quantity of stearyl ethyl acid o-phosphate present ranging from about 0.1% to about 10%, based on the weight of the treated material, so as to be sufficient to prevent the accumulation of electrical charges in said textile material.
5. Textile material containing in amount suincient to prevent the accumulation of electrical charges in said textile materials a dialkyl acid o-phosphate wherein one of the alkyl groups has from 6 to 18 carbon atoms and the other from 1 to 4 carbon atoms.
v 6. Textile material containing a textile lubricating oil and a dialkyl acid o-phosphate wherein one of the alkyl groups has from 6 to 18 carbon REFERENCES CITED atoms and the other from 1 to 4 carbon atoms. said phosphate being present in amount sumcient The following references are of record in the to prevent the accumulation of electrical charges file of this patent:
in said textile material.
7. A cellulose ester textile material contain- UNITED STATES PATENTS ing in amount suflicient to prevent the accumula-- N ber Name Date tion of electrical charges in said textile materials 1,914,331 Nuesslein et al June 13, 1933 a, dialkyl acid o-phosphate wherein one of the 2,005,619 Graves June 18, 1935 alkyl groups has from 6 to 18 carbon atoms and 10 2,080,299 Bennlng et'al. May 11, 1937 the other from 1 to 4 carbon atoms. 2,345,734 Dickey et a1. Apr. 4, 1944 ARTHUR L. FOX.
Claims (1)
1. TEXTILE MATERIAL CONTAINING FROM ABOUT 99 TO ABOUT 90 PARTS OF A TEXTILE LUBRICATING OIL AND FROM ABOUT 1 TO ABOUT 10 PARTS OF A DIALKYL ACID OPHOSPHATE WHEREIN ONE OF THE ALKYL GROUPS HAS FROM 6 TO 18 CARBON ATOMS AND THE OTHER FROM 1 TO 4 CARBON ATOMS, THE QUANTITY OF DIALKYL ACID O-PHOSPHATE PRESENT RANGING FROM ABOUT 0.1% TO ABOUT 10%, BASED ON THE WEIGHT OF THE TREATED MATERIAL, SO AS TO BE SUFFICIENT TO PREVENT THE ACCUMULATION OF ELECTRICAL CHARGES IN SAID TEXTILE MATERIAL.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE469632D BE469632A (en) | 1945-12-06 | ||
| US633266A US2498408A (en) | 1945-12-06 | 1945-12-06 | Antistatic textile materials |
| GB29565/46A GB629659A (en) | 1945-12-06 | 1946-10-03 | Anti-static textile materials |
| FR937525D FR937525A (en) | 1945-12-06 | 1946-11-29 | Textile processing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US633266A US2498408A (en) | 1945-12-06 | 1945-12-06 | Antistatic textile materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2498408A true US2498408A (en) | 1950-02-21 |
Family
ID=24538948
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US633266A Expired - Lifetime US2498408A (en) | 1945-12-06 | 1945-12-06 | Antistatic textile materials |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2498408A (en) |
| BE (1) | BE469632A (en) |
| FR (1) | FR937525A (en) |
| GB (1) | GB629659A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2575382A (en) * | 1949-12-21 | 1951-11-20 | Celanese Corp | Fiber lubricant composition |
| US2743193A (en) * | 1953-08-10 | 1956-04-24 | Eastman Kodak Co | Treated cellulose organic acid ester fibers |
| US2978440A (en) * | 1955-11-29 | 1961-04-04 | Union Carbide Corp | Anti-static vinyl chloride copolymer containing salts of dialkyl phosphates |
| US3144671A (en) * | 1958-04-04 | 1964-08-18 | Dow Chemical Co | Dust cloth |
| US3341343A (en) * | 1963-11-12 | 1967-09-12 | Gen Anilline & Film Corp | Hydrophobic polymeric resin containing phosphate ester antistatic agent and process for producing antistatic properties |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE975308C (en) * | 1953-12-21 | 1961-11-02 | Boehme Fettchemie G M B H | Antistatic rendering of finished textile fabrics or knitted fabrics made from fully synthetic fiber material |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1914331A (en) * | 1929-12-18 | 1933-06-13 | Ig Farbenindustrie Ag | Treatment of textile materials with aqueous liquids |
| US2005619A (en) * | 1934-11-10 | 1935-06-18 | Du Pont | Esters of acids of phosphorus |
| US2080299A (en) * | 1935-04-12 | 1937-05-11 | Du Pont | Inhibiting corrosion of metals |
| US2345734A (en) * | 1939-07-18 | 1944-04-04 | Eastman Kodak Co | Self-emulsifying phosphated and phosphited oils as antistatic lubricants |
-
0
- BE BE469632D patent/BE469632A/xx unknown
-
1945
- 1945-12-06 US US633266A patent/US2498408A/en not_active Expired - Lifetime
-
1946
- 1946-10-03 GB GB29565/46A patent/GB629659A/en not_active Expired
- 1946-11-29 FR FR937525D patent/FR937525A/en not_active Expired
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1914331A (en) * | 1929-12-18 | 1933-06-13 | Ig Farbenindustrie Ag | Treatment of textile materials with aqueous liquids |
| US2005619A (en) * | 1934-11-10 | 1935-06-18 | Du Pont | Esters of acids of phosphorus |
| US2080299A (en) * | 1935-04-12 | 1937-05-11 | Du Pont | Inhibiting corrosion of metals |
| US2345734A (en) * | 1939-07-18 | 1944-04-04 | Eastman Kodak Co | Self-emulsifying phosphated and phosphited oils as antistatic lubricants |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2575382A (en) * | 1949-12-21 | 1951-11-20 | Celanese Corp | Fiber lubricant composition |
| US2743193A (en) * | 1953-08-10 | 1956-04-24 | Eastman Kodak Co | Treated cellulose organic acid ester fibers |
| US2978440A (en) * | 1955-11-29 | 1961-04-04 | Union Carbide Corp | Anti-static vinyl chloride copolymer containing salts of dialkyl phosphates |
| US3144671A (en) * | 1958-04-04 | 1964-08-18 | Dow Chemical Co | Dust cloth |
| US3341343A (en) * | 1963-11-12 | 1967-09-12 | Gen Anilline & Film Corp | Hydrophobic polymeric resin containing phosphate ester antistatic agent and process for producing antistatic properties |
Also Published As
| Publication number | Publication date |
|---|---|
| BE469632A (en) | 1900-01-01 |
| GB629659A (en) | 1949-09-26 |
| FR937525A (en) | 1948-08-19 |
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