US3622378A - Fibers with anionic-cationic finish - Google Patents
Fibers with anionic-cationic finish Download PDFInfo
- Publication number
- US3622378A US3622378A US751345A US3622378DA US3622378A US 3622378 A US3622378 A US 3622378A US 751345 A US751345 A US 751345A US 3622378D A US3622378D A US 3622378DA US 3622378 A US3622378 A US 3622378A
- Authority
- US
- United States
- Prior art keywords
- cationic
- anionic
- percent
- finish
- weight
- 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
- 239000000835 fiber Substances 0.000 title abstract description 28
- 125000000129 anionic group Chemical group 0.000 abstract description 16
- 125000002091 cationic group Chemical group 0.000 abstract description 14
- 125000004432 carbon atom Chemical group C* 0.000 abstract description 13
- 239000004094 surface-active agent Substances 0.000 abstract description 13
- 239000000203 mixture Substances 0.000 abstract description 12
- 125000003342 alkenyl group Chemical group 0.000 abstract description 11
- 125000000217 alkyl group Chemical group 0.000 abstract description 11
- 239000004753 textile Substances 0.000 abstract description 11
- 239000003945 anionic surfactant Substances 0.000 abstract description 10
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract description 4
- 239000011248 coating agent Substances 0.000 abstract description 3
- 238000000576 coating method Methods 0.000 abstract description 3
- 239000005002 finish coating Substances 0.000 abstract description 3
- 239000003093 cationic surfactant Substances 0.000 description 13
- 239000007787 solid Substances 0.000 description 11
- 239000004615 ingredient Substances 0.000 description 9
- -1 hydroxyethyl groups Chemical group 0.000 description 7
- 239000002280 amphoteric surfactant Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 4
- 230000005611 electricity Effects 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000019270 ammonium chloride Nutrition 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- QHAUASBJFFBWMY-UHFFFAOYSA-N didecyl hydrogen phosphate Chemical compound CCCCCCCCCCOP(O)(=O)OCCCCCCCCCC QHAUASBJFFBWMY-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-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
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 150000001449 anionic compounds Chemical class 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- SNAMIIGIIUQQSP-UHFFFAOYSA-N bis(6-methylheptyl) hydrogen phosphate Chemical compound CC(C)CCCCCOP(O)(=O)OCCCCCC(C)C SNAMIIGIIUQQSP-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 239000002752 cationic softener Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 125000002704 decyl 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])* 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 230000003670 easy-to-clean Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940078490 n,n-dimethylglycine Drugs 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002897 organic nitrogen compounds Chemical class 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003760 tallow 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
- D06M13/322—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 nitrogen
- D06M13/325—Amines
- D06M13/342—Amino-carboxylic acids; Betaines; Aminosulfonic acids; Sulfo-betaines
-
- 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
- D06M13/322—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 nitrogen
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
-
- 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
- Y10T428/2967—Synthetic resin or polymer
- Y10T428/2969—Polyamide, polyimide or polyester
Definitions
- the invention in its broad scope is defined as a textile fiber containing on its surface from 0.06 percent to 3 percent by weight of a finish comprising an organic anionic, an organic cationic, and an organic amphoteric surfactant, the amount of amphoteric being at least 3 percent of the total solids weight of the finish composition.
- the invention in its narrower aspect is defined as a textile fiber having a finish coating of compatibilized cationic and anionic components comprising from 0.06 percent to about 3 percent by weight of the fiber, said coating comprising a mixture of (a) an organic anionic surfactant containing at least one alkyl or alkenyl group having from eight to 20 carbon atoms; (b) an organic cationic nitrogen containing surfactant having at least one long chain alkyl or alkenyl group of eight to about 20 carbon atoms; and (c) a compatibilizing quantity of an organic amphoteric nitrogen containing surfactant having at least one alkyl or alkenyl group of eight to 20 carbon atoms.
- organic anionic surfactants and organic cationic surfactants are compatibilized in a textile fiber finish by inclusion in the finish bath of at least 3 percent, based on the combined solids weight of the anionic and cationic ingredients, of an organic amphoteric compound.
- the inclusion of the amphoteric precludes precipitation and sludge formation in the composite finish.
- organic cationic surfactant refers to a salt that dissociates in solution into an organic cationic surfactant.
- the organic cationic surfactants included in the chemical combination of this invention are organic nitrogen compounds having at least one long chain alkyl or alkenyl group of eight to about 20 carbon atoms.
- the most preferred cationic surfactants contain a quaternary nitrogen atom.
- Typical organic cationic salts useful as surfactants in the practice of this invention comprise:
- An organic amphoteric surfactant refers to an organic surfactant having both acid and basic properties.
- the amphoteric surfactants useful in the practice of the present invention are defined as nitrogen-containing organic compounds having at least one alkyl or alkenyl group of eight to 20 carbon atoms. The most preferred contain a carboxyl group or the sodium salt of a carboxyl group.
- Typical amphoteric surfactants useful in the practice of this invention comprise:
- TAB LE III.AMPHOTE RIC S URFAC'IANIS Name Structure a. Disodium N -lauryl-fi-iminodipropionate O O O b. N-oleyl-N, N-dimethyl glycine H H CHa ⁇ /C ⁇ Q N /C O oleyl CH 0 DlSodium N-tallow-fi-imlnodipropionate. .o Same as (a) except lauryl group replaced with a tallow group (mostly stearyl-IB carbon atoms and saturated; and oleyl-18 carbon atoms and unsaturated).
- the new finish combination is preferably made up in batch plied as a predraw application or postdraw application or even form and then applied to the textile fiber.
- the new as an overlay finish. combination may be applied to the fiber in stepwise fashion;
- the invention includes any known textile fiber and is parfor example, the anionic agent may be applied to the fiber at ticularly advantageous with fibers based on polymers and one point in the process and, at a later point, the cationic and copolymers of polyethylene terephthalate, nylon, and
- amphoteric compounds may be applied.
- polyacrylonitrile polyacrylonitrile.
- These fibers have a high volume in the approcess, it is preferable to avoid mixing the anionic and caparel markets where adequate finishing techniques are detionic ingredients before the amphoteric is admixed. in many manded to prevent the fiber from irritating the skin or from cases, however, the amphoteric destroys the precipitate being excessively electrostatic.
- the amphoteric compound is added to a vessel EXAMPLES lXlll containing the required volume of water. Then, the anionic and cationic ingredients are admixed. Usually, concentrations of from I to 20 percent solids of the new finish combination in These examples Show the amount of amPhotelric Compound water are applied to running fib b means f a fi i h necessary to compatibilize the anionic and cationic surfacplicator. Applications to produce a solids content of finish intants Show" in the above tables in propo tions.
- gredients on the finished yarn of from 0.06 percent to 3 per-
- a beaker containing a volume of water is added an cent based on the total weight of the finished yarn are satisfacamphoten'c surfactant selected from table lll, an anionic surtory.
- factant selected from table ll and a cationic surfactant The new finish combination or any ingredient thereof may selected from table I.
- the amount of amphoteric necessary to be applied to textile fibers at any place in the production compatibilize the cationic to anionic is recorded. Results are process.
- the combination or any part thereof can be apas follows:
- Finish solution Amphoteric concentration surfactant (percent from solids in Table III water) Anionic surfactant Table II Cationic surfactant Minimum percent by weight I of amphoteric to compatibilize EXAMPLES XIV-XVII These examples show the application of the finish combinations to textile fibers and show improvement in static electricity properties of the fibers resulting thereby.
- the static electricity measurements are determined as follows: A Beckman Micro-microammeter Model-5 manufactured by Beckman Instruments Inc., Fullerton, Calif. with a DC potential of 210 volts and a resistance of l megohm is set up. A thin plate of electrically resistant material having four metal prongs mounted perpendicularly at each comer of a 1.25 inch square (3.2 cm. square) thereon is fabricated and connected to the Micro-microammeter in such a way that upon connecting two pairs of prongs (one pair to negative and one pair to positive 210 volts) current will flow in the system when a sample is on the prongs. The yarn to be tested for static electricity is wound on a 3-in. (7.6 cm.) long 2-in.
- the core containing the yarn is placed lengthwise against the four prongs of the electrical system, and the amount of current flowing through the circuit is measured. Knowing the potential and the amount of current, the resistance is calculated and its logarithm is recorded.
- finish compositions are metered onto the yarn from aqueous solution by means of a metering pipette.
- Ill. 75-denier/30-filament yam comprising a copolymer of 94 percent acrylonitrile and 6 percent methyl acrylate having 0.3 2" turns per inch (0.12 toms/cm.) twist and 0.4 percent "no,
- the yarn is finished to a level of 0.2 percent by weight solids finish ingredients based on the weight of the finished yarn.
- EXAMPLE XV The same nylon starting material as used for example XIV is 20 covered with a 10 percent aqueous finish composition comprising 10 parts by weight of the amphoteric surfactant of table Ill-a, 10 parts by weight of the cationic surfactant of table l-a and 80 parts by weight of the anionic surfactant of table "-0.
- the yarn is finished to a level of 0.5 percent by weight solids finish based on the weight of the finished yarn.
- Log R at 65 percent relative humidity is 7.5.
- EXAMPLE XVI The polyethylene terephthalate yarn is coated with a 20 percent by weight aqueous solution comprising the complex anionic surfactant formed by combining 1 1.6 parts by weight of monoand didecyl-phosphoric acids percent mono 50 percent di) with 8.4 parts of triethanolamine, 40 parts by weight of a nonionic surfactant of a 12- to l8-carbon synthetic primary alcohol condensed with polyoxyethylene so that the weight of polyoxyethylene is percent of the total weight of the molecule, and 20 parts of the amphoteric of table llld, and 20 parts by weight of the cationic surfactant of table l-b.
- Log R value of the finished yarn is 7.5 as compared to a Log R value of 17.2 for an identical yarn containing no finish on its surface.
- EXAMPLE XVll The yarn of acrylonitrile and methylacrylate is coated with a 20 percent by weight aqueous solution comprising 10 parts by weight of a cationic surfactant consisting of dicocodimethylammonium chloride, 30 parts by weight of the amphoteric of table lll-a, 10 parts by weight of the anionic used in example XVI and 50 parts by weight of the nonionic surfactant used in example XVI.
- the yarn is finished to a level of 0.2 percent by weight solids finish based on the total weight of the finished yarn.
- the Log R value is 11.8 at 20 percent relative humidity as compared to a Log R value of 16.9 for an identical yam having no finish on its surface.
- EXAMPLE XVlll This example shows the combination, in a single bath, of cationic and anionic surfactants in a composition containing other ingredients, by use of an amphoteric surfactant.
- a vessel containing a volume of water is added 3 parts, by weight, of the amphoteric of table Ill-a, 27.7 parts, by weight, of a cationic surfactant comprising the reaction product of stearic acid and diethanolamine quaternized with dimethylsulfate; and 69.3 parts of a mixture comprising 16.6 parts of an anionic surfactant comprising sulfated peanut oil partially neutralized with sodium hydroxide, 8.2 parts by weight of to have excellent antistatic and frictional properused as a predraw finish on nylon yarn, and the r comprises including in the composition an organic amphoteric nitrogen-containing group of eight to 20 surfactant being sufficient to prevent surfactants (a) and (b) from precipitating.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US75134568A | 1968-08-09 | 1968-08-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3622378A true US3622378A (en) | 1971-11-23 |
Family
ID=25021581
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US751345A Expired - Lifetime US3622378A (en) | 1968-08-09 | 1968-08-09 | Fibers with anionic-cationic finish |
Country Status (6)
Country | Link |
---|---|
US (1) | US3622378A (en, 2012) |
BE (1) | BE737261A (en, 2012) |
CH (1) | CH1203269D (en, 2012) |
DE (1) | DE1940538A1 (en, 2012) |
FR (1) | FR2015391A7 (en, 2012) |
GB (1) | GB1246521A (en, 2012) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3868270A (en) * | 1972-12-04 | 1975-02-25 | Du Pont | Fibers with finish containing organic phosphates and sulphates |
US4118327A (en) * | 1977-03-28 | 1978-10-03 | Colgate Palmolive Company | Fabric softener and anti-static compositions |
US4144177A (en) * | 1976-10-19 | 1979-03-13 | Kao Soap Co., Ltd. | Softener composition for fabrics |
US20060038157A1 (en) * | 2002-02-06 | 2006-02-23 | Wolfgang Becker | Use of ethoxylated fatty acids as smoothing agents for synthetic and natural fibres |
US20080005852A1 (en) * | 2004-07-27 | 2008-01-10 | Nano-Tex, Inc. | Durable multifunctional finishing of fabrics |
US20120070481A1 (en) * | 2006-12-14 | 2012-03-22 | Church & Dwight Co., Inc. | Stable aqueous solutions of silane quat ammonium compounds |
EP3415685A1 (de) | 2017-06-14 | 2018-12-19 | Rudolf GmbH | Zusammensetzung und deren verwendung zur ausrüstung von fasern und textilien |
WO2018229111A1 (de) | 2017-06-14 | 2018-12-20 | Rudolf Gmbh | Zusammensetzung und deren verwendung zur ausrüstung von fasern und textilien |
WO2018229116A1 (de) | 2017-06-14 | 2018-12-20 | Rudolf Gmbh | Zusammensetzung und deren verwendung zur ausrüstung von textilien |
WO2025006415A3 (en) * | 2023-06-28 | 2025-05-08 | The Penn State Research Foundation | Surface-modified textiles |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3003954A (en) * | 1957-07-19 | 1961-10-10 | Staley Mfg Co A E | Methods and compositions of matter for softening textile fibers, yarns, and fabrics |
US3093591A (en) * | 1957-05-03 | 1963-06-11 | Gen Mills Inc | Compositions containing nu-alkyl-betaamino propionates and germicidal quaternary ammonium compounds |
US3105500A (en) * | 1959-08-04 | 1963-10-01 | American Cyanamid Co | Soil retaining finish for textiles |
US3277079A (en) * | 1964-01-29 | 1966-10-04 | Jack J Press | Organic complex for use as an anti-static agent |
US3402127A (en) * | 1964-11-23 | 1968-09-17 | Monsanto Co | Synthetic thermoplastic yarn finish |
-
0
- CH CH1203269D patent/CH1203269D/xx unknown
-
1968
- 1968-08-09 US US751345A patent/US3622378A/en not_active Expired - Lifetime
-
1969
- 1969-08-07 GB GB39574/69A patent/GB1246521A/en not_active Expired
- 1969-08-08 DE DE19691940538 patent/DE1940538A1/de active Pending
- 1969-08-08 BE BE737261D patent/BE737261A/xx unknown
- 1969-08-08 FR FR6927444A patent/FR2015391A7/fr not_active Expired
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3093591A (en) * | 1957-05-03 | 1963-06-11 | Gen Mills Inc | Compositions containing nu-alkyl-betaamino propionates and germicidal quaternary ammonium compounds |
US3003954A (en) * | 1957-07-19 | 1961-10-10 | Staley Mfg Co A E | Methods and compositions of matter for softening textile fibers, yarns, and fabrics |
US3105500A (en) * | 1959-08-04 | 1963-10-01 | American Cyanamid Co | Soil retaining finish for textiles |
US3277079A (en) * | 1964-01-29 | 1966-10-04 | Jack J Press | Organic complex for use as an anti-static agent |
US3402127A (en) * | 1964-11-23 | 1968-09-17 | Monsanto Co | Synthetic thermoplastic yarn finish |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3868270A (en) * | 1972-12-04 | 1975-02-25 | Du Pont | Fibers with finish containing organic phosphates and sulphates |
US4144177A (en) * | 1976-10-19 | 1979-03-13 | Kao Soap Co., Ltd. | Softener composition for fabrics |
US4118327A (en) * | 1977-03-28 | 1978-10-03 | Colgate Palmolive Company | Fabric softener and anti-static compositions |
US20060038157A1 (en) * | 2002-02-06 | 2006-02-23 | Wolfgang Becker | Use of ethoxylated fatty acids as smoothing agents for synthetic and natural fibres |
US20080005852A1 (en) * | 2004-07-27 | 2008-01-10 | Nano-Tex, Inc. | Durable multifunctional finishing of fabrics |
US20120070481A1 (en) * | 2006-12-14 | 2012-03-22 | Church & Dwight Co., Inc. | Stable aqueous solutions of silane quat ammonium compounds |
US8728540B2 (en) * | 2006-12-14 | 2014-05-20 | Church & Dwight Co., Inc. | Stable aqueous solutions of silane quat ammonium compounds |
EP3415685A1 (de) | 2017-06-14 | 2018-12-19 | Rudolf GmbH | Zusammensetzung und deren verwendung zur ausrüstung von fasern und textilien |
WO2018229111A1 (de) | 2017-06-14 | 2018-12-20 | Rudolf Gmbh | Zusammensetzung und deren verwendung zur ausrüstung von fasern und textilien |
WO2018229116A1 (de) | 2017-06-14 | 2018-12-20 | Rudolf Gmbh | Zusammensetzung und deren verwendung zur ausrüstung von textilien |
WO2025006415A3 (en) * | 2023-06-28 | 2025-05-08 | The Penn State Research Foundation | Surface-modified textiles |
Also Published As
Publication number | Publication date |
---|---|
CH1203269D (en, 2012) | |
BE737261A (en, 2012) | 1970-01-16 |
FR2015391A7 (en, 2012) | 1970-04-24 |
DE1940538A1 (de) | 1970-03-26 |
GB1246521A (en) | 1971-09-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3622378A (en) | Fibers with anionic-cationic finish | |
Weatherburn et al. | The sorption of synthetic surface-active compounds by textile fibers | |
US2734830A (en) | ||
US3003954A (en) | Methods and compositions of matter for softening textile fibers, yarns, and fabrics | |
GB1593187A (en) | Softener composition for fabrics | |
US2694688A (en) | Antistatic compositions for textiles | |
US3048539A (en) | Antistatic textile lubricant finishes | |
CA1085562A (en) | Compositions for souring and softening laundered textile materials, method of preparing the same, and stock solutions prepared therefrom | |
US2832696A (en) | Method for applying antistatic agents to polyethylene and destaticized polyethylene articles thereby obtained | |
US2723246A (en) | Antistatic compositions | |
US3515580A (en) | Urea/salt of an acid complex and a wetting agent - antistatic composition for synthetic polymers | |
US3468697A (en) | Method of treating textile articles which are usually laundered | |
US3788888A (en) | Fiber-lubricant composition | |
Vauquelin et al. | Agonist‐mediated conformational changes of muscarinic receptors in rat brain | |
US2815301A (en) | Antistatic synthetic fibers | |
US3716393A (en) | Process for antistatically treating articles | |
PT95604A (pt) | Processo para a fabricacao de fibras de aramida com acabamento isento de deposito | |
US3625891A (en) | Wash cycle fabric softeners and method of preparing and using same | |
US2700001A (en) | Process of providing textile material with an antistatic finish | |
US2729577A (en) | Method of imparting antistatic properties to textile materials | |
US3511704A (en) | Electrically conductive flock for electrostatic flocking | |
DE1544670A1 (de) | Antistatische Formmassen aus Polystyrol | |
US3277079A (en) | Organic complex for use as an anti-static agent | |
US3775446A (en) | Acyl-amino-propyl-dialkylammonium dialkyl phosphates | |
US3258358A (en) | Process for producing an antistatic finish on hydrophobic materials |