US20020019460A1 - Synthetic fiber treatment agent composition - Google Patents
Synthetic fiber treatment agent composition Download PDFInfo
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- US20020019460A1 US20020019460A1 US09/835,428 US83542801A US2002019460A1 US 20020019460 A1 US20020019460 A1 US 20020019460A1 US 83542801 A US83542801 A US 83542801A US 2002019460 A1 US2002019460 A1 US 2002019460A1
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- synthetic fiber
- treatment agent
- agent composition
- fiber treatment
- component
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- ACZZVVOHZBLOFT-UHFFFAOYSA-N CC(C)(C)(C)CCCNCCN Chemical compound CC(C)(C)(C)CCCNCCN ACZZVVOHZBLOFT-UHFFFAOYSA-N 0.000 description 1
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- RBVXOFRVMBXNSC-UHFFFAOYSA-N 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C[Si](C)(O)O[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](C)(CCCNCCN)O[SiH]=O Chemical compound C[Si](C)(O)O[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](C)(CCCNCCN)O[SiH]=O ZGABMZSUMUTPEL-UHFFFAOYSA-N 0.000 description 1
- POWUHWUPSHKOLF-UHFFFAOYSA-N [H]O[SiH2][Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)O[Si](C)(CCCNC)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)O[Si](C)(C)O Chemical compound [H]O[SiH2][Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)O[Si](C)(CCCNC)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)O[Si](C)(C)O POWUHWUPSHKOLF-UHFFFAOYSA-N 0.000 description 1
- NRFPOWPEHOFJSL-UHFFFAOYSA-N [H]O[SiH2][Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)O[Si](C)(O)CCCNC Chemical compound [H]O[SiH2][Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)[Si](=O)O[Si](C)(O)CCCNC NRFPOWPEHOFJSL-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
- D06M15/6436—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing amino groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
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- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
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- 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
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- 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
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- 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
- D06M2200/50—Modified hand or grip properties; Softening compositions
Abstract
A synthetic fiber treatment agent composition capable of providing synthetic fibers, particularly synthetic fiber padding, with a better hand, smoothness, repulsion, and the like. The composition comprises an amino group-containing polyorganosiloxane with a high amino group content and specific terminal groups, and an amino group-containing polydiorganosiloxane with a low amino group content or a polydiorganosiloxane with no amino groups.
Description
- The present invention relates to a synthetic fiber treatment agent composition, and in particular to a synthetic fiber treatment agent composition capable of providing synthetic fiber padding with better smoothness, repulsion, and the like.
- Polyester fibers or acrylic fibers have been used conventionally for the synthetic fibers of padding. Polyester fibers in particular have a higher compression modulus and better recovery than synthetic fibers such as nylon, polyvinyl chloride, or polypropylene, making them suitable for mattress padding, pillows, cushions, costume padding, and the like. Many silicone-based fiber treatment agents have thus far been proposed to provide such polyester and acrylic fibers with better smoothness and repulsion. Examples include a treatment agent comprising a high molecular weight polydimethylsiloxane and an amino group-containing alkoxysilane (JP Patent Application Publication No. Sho 51-37996), treatment agents based on an epoxy group-containing siloxane and an amino group-containing alkoxysilane (JP Patent Application Publication Nos. Sho 53-19715 and Sho 53-19716), a treatment agent comprising an amino group-containing siloxane, epoxy group-containing siloxane, and amino group-containing alkoxysilane (JP Patent Application Publication No. Sho 58-1231), and treatment agents based on an amino group-containing siloxane and an amino group-containing alkoxysilane (JP Patent Application Publication No. Sho 58-17310 and JP Patent Application Laying Open No. Hei 7-305278). However, such treatment agents require an alkoxysilane to be blended in as a component for providing smoothness, resulting in alcohol by-products from the alkoxysilane during treatment. Treatment agents in which methoxysilane has been blended, for example, result in methanol by-products, and run the risk of polluting the working environment and of causing explosions.
- As a result of extensive research to overcome such drawbacks, the inventors perfected the present invention upon discovering the effectiveness of combining an amino group-containing polyorganosiloxane with a high amino group content and specific terminal groups, and an amino group-containing polydiorganosiloxane with a low amino group content or a polydiorganosiloxane with no amino groups.
- An object of the present invention is to provide a synthetic fiber treatment agent composition capable of providing synthetic fibers, particularly synthetic fiber padding, with better hand, smoothness, repulsion, and the like.
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- where R, R2, R3, R4, and a are the same as above and
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- where A is selected from a group consisting of trialkylsilyl, a hydrogen atom, and a C1 to C20 optionally substitutable monovalent hydrocarbon group; R, R2, R3, R4, and a are the same as above; x is an integer of 1 or more; and y is 0 or an integer of 1 or more, where y/(x+y) is no more than 0.1.
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- where R, R2, R3, R4, and a are the same as above, and
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- where A is a trialkylsilyl group, a hydrogen atom, or a C1 to C20 optionally substitutable monovalent hydrocarbon group; R, R2, R3, R4, and a are the same as above; x is an integer of 1 or more; and y is 0 or an integer of 1 or more, where y/(x+y) is no more than 0.1.
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- In the formulas, R is a C1 to C20 optionally substitutable monovalent hydrocarbon or hydroxyl group, with at least 80 mol % of all R comprising monovalent hydrocarbon groups. Examples of monovalent hydrocarbon groups include saturated aliphatic hydrocarbon groups such as methyl, ethyl, propyl, butyl, octyl, decyl, dodecyl, and tetradecyl; unsaturated aliphatic hydrocarbon groups such as vinyl and allyl; saturated alicyclic groups such as cyclopentyl and cyclohexyl; aromatic hydrocarbon groups such as phenyl, tolyl, and naphthyl; and such groups where some of the hydrogen atoms have been substituted with organic groups containing epoxy groups, halogen atoms, or the like. R may be the same or different, but is preferably a methyl group. R2 is a C1 to C10 divalent hydrocarbon group, such as alkylene, arylene, or alkenylene. R2 is preferably an ethylene or propylene group. R3 and R4 are hydrogen atoms or C1 to C20 optionally substitutable monovalent hydrocarbon groups. Specific examples of monovalent hydrocarbon groups include the same groups as those given for R. R3 and R4 may be the same or different, but are preferably hydrogen atoms. The symbol a is an integer from 0 to 5, but is preferably 0 or 1. The symbol p is an integer from 0 to 2, q is an integer from 0 to 3, and r is 0 or 1, where (p+q+r)=3. The content of the aforementioned amino group-containing diorganosiloxane units are at least 30 mol % of the total siloxane units, preferably at least 50 mol %, and even more preferably at least 70 mol %. This is because the intended effects are less likely to be achieved when the proportion of amino group-containing diorganosiloxane units is less than 30 mol %. Examples of units other than the aforementioned amino group-containing diorganosiloxane units of this component forming the polyorganosiloxane include siloxane units represented by R2SiO2/2, RSiO3/2, R4—NH—(CH2CH2NR3)a-R2-SiO3/2, R3SiO1/2, and SiO4/2 (where R, R2, R3, R4, and a are the same as above). The proportion of such siloxane units is limited only to the extent that the effects of the present invention are not compromised. The molecular structure of this component is preferably linear or linear with partial branches. The viscosity of component (A) at 25° C. is usually 10 to 100,000 mm2/s, and the degree of polymerization of linear polyorganosiloxanes is preferably within the range of 2 to 1000, and more preferably 10 to 500. An example of a method for producing component (A) is to add an excess amount of water to N-β-(aminoethyl)-γ-aminopropylmethyldimethoxysilane, heat the mixture to 70° C. to ensure complete hydrolysis, and then heat the product at reduced pressure to remove the methanol and water. In another method, N-β-(aminoethyl)-γ-aminopropylmethyldimethoxysilane is mixed with silanol-terminated polydimethylsiloxane, an excess amount of water and potassium hydroxide are added, the material is heated, the aminosilane is hydrolyzed at 70° C., and the aminosilane hydrolysate and silanol-terminated polydimethylsiloxane are copolymerized as the water and methanol are removed at 90° C.
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- In the formula, A is selected from the group consisting of trialkylsilyl, hydrogen atom, and C1 to C20 optionally substitutable monovalent hydrocarbon groups, and is preferably a hydrogen atom or monovalent hydrocarbon group. Specific examples of monovalent hydrocarbons include the same as those for R above, although alkyl groups are preferred. The symbol x is an integer of 1 or more; and y is 0 or an integer of 1 or more. Although the maximum for x and y is not particularly limited, the value selected should result in a polydiorganosiloxane having a viscosity of at least 50 mm2/s in order to provide softness, smoothness, and repulsion. A viscosity of 300 to 30,000 mm2/s is even more desirable. The ratio y/(x+y) is no more than 0.1, and preferably no more than 0.02. A value greater than 0.1 will not provide satisfactory smoothness, and will result in pronounced yellowing caused by the amino groups. Although R, R2, R3, R4, and a are the same as above, at least 80 mol % of R should be methyl groups in order to provide the fiber with a better hand. Amino groups represented by —R2—(NR3CH2CH2)a—NH—R4 are commonly groups represented by —C3H6—(NHCH2CH2)aNH2.
- The method for producing component (B) is not particularly limited. In one specific example, a polydimethylsiloxane blocked at both ends with silanol groups and N-β-(aminoethyl)-γ-aminopropylmethyldimethoxysilane are allowed to react for a specified time at 90° C. in the presence of a basic catalyst such as potassium hydroxide, and the basic catalyst is then neutralized with an acid. Component (B) may be one type structure used by itself, or a mixture of two or more different types of structures. Preferred mixtures include a polydiorganosiloxane containing no amino groups, where y in the aforementioned formula is 0, and a polydiorganosiloxane that contains amino groups, where y is 1 or more. The mixing ratio preferably ranges from 1:99 to 99:1.
-
- Components (A) and (B) are preferably blended in a ratio of 1 to 50 weight parts, and even more preferably 2 to 30 weight parts component (A) per 100 weight parts component (B).
- The present composition is based on the aforementioned components (A) and (B), but other components may also be added as needed, such as antistatic agents, non-silicone-based organic softeners, alkoxysilanes, or partial hydrolysates thereof, which have reactive groups such as amino groups or epoxy groups, alkylalkoxysilanes or partial hydrolysates thereof, preservatives, and anti-mildewing agents. When fiber yellowing caused by the amino groups in the present composition becomes a problem, compounds having groups that are reactive with amino groups such as epoxy compounds or organic acids or their anhydrides can be added to suppress yellowing caused by amino groups.
- The present composition is usually diluted with a solvent and adjusted to the prescribed concentration, or is emulsified and dispersed in water using a surfactant to produce an emulsion, which is then diluted with water and adjusted to the prescribed concentration before use. Emulsion dispersions in water are particularly desirable. Examples of surfactants which may be used for emulsification include polyoxyethylene alkyl ethers or polyoxyethylene-polyoxypropylene alkyl ethers, which have alkyl groups such as lauryl, cetyl, stearyl, or trimethylnonyl groups; polyoxyethylene alkylphenyl ethers having alkylphenyl groups such as nonylphenyl or octylphenyl; polyethylene glycol fatty acid esters comprising the addition polymerization of ethylene oxide to fatty acids such as stearic acid or oleic acid; nonionic surfactants such as polyoxyethylene glycerin fatty acid esters and polyglycerin fatty acid esters; anionic surfactants such as alkylsulfates and alkylbenzenesulfonates; cationic surfactants such as quaternary ammonium salts and alkylamine salts; and amphoteric surfactants such as alkylbetaines and alkylimidazolines. Examples of ways to prepare emulsions include methods in which components (A) and (B) are separately emulsified using the aforementioned surfactants, and the two emulsions are then mixed; and methods in which components (A) and (B) are mixed, and are then emulsified using the aforementioned surfactants. Examples of emulsifying devices which may be used include homomixers, homogenizers, propeller-bladed agitators, line mixers, and colloid mills. The polyorganosiloxane of component (A) is water-soluble when containing a large amount of the aforementioned amino group-containing diorganosiloxane units. In such cases, therefore, the emulsion of component (B) can be prepared, and component (A) can then be blended therein as such, or an aqueous solution of component (A) can be prepared first, and then blended in an emulsion of component (B). When fibers are treated, a solution or emulsion of the composition of the present invention is applied to the fibers by impregnation, spraying, or another means, and the fibers are then preferably dried and heat treated. When an emulsion of the present composition is used, the amount applied to the fibers should result in 0.1 to 3 wt % composition in terms of solids.
- The present composition characteristically provides synthetic fibers, particularly synthetic fiber padding, with excellent hand, smoothness, repulsion, and the like. The present invention is, in particular, able to provide smoothness as good as that provided by alkoxysilanes conventionally used to provide smoothness, but without the use of such alkoxysilanes. Another advantage is the extremely low level of alcohol by-products during treatment.
- The present invention is illustrated in detail in the following examples. Parts in the examples are based on weight, and the viscosity was determined at 25° C.
- Synthesis of polyorganosiloxane (A) containing amino groups. 20 Parts water were added to 100 parts N-β-(aminoethyl)-γ-aminopropylmethyldimethoxysilane, and the mixture was stirred for 2 hours at 70° C. The methanol and water were then removed at 90° C. under reduced pressure to synthesize the water-soluble amino group-containing polyorganosiloxane (A) described by formula
-
-
- Synthesis of polyorganosiloxane (D) containing amino groups. 4.3 parts water were added to 100 parts N-β-(aminoethyl)-γ-aminopropylmethyldimethoxysilane, and the mixture was stirred for 2 hours at 70° C. The methanol was then removed at 60° C. under reduced pressure to synthesize amino group-containing polyorganosiloxane (D) described by formula
-
-
-
-
- Preparation of aqueous solutions of amino group-containing polyorganosiloxanes (A) through (D). 50 Parts of the amino group-containing polyorganosiloxane (A) obtained in Synthesis Example 1 were mixed with 50 parts water to prepare a 50 wt % aqueous solution (SA). 50 Parts of the amino group-containing polyorganosiloxane (B) obtained in Synthesis Example 2 were mixed with 50 parts water to prepare a 50 wt % aqueous solution (SB). 50 Parts of the amino group-containing polyorganosiloxane (C) obtained in Synthesis Example 3 were mixed with 50 parts water to prepare a 50 wt % aqueous solution (SC). 50 Parts of the amino group-containing polyorganosiloxane (D) obtained in Synthesis Example 4 were mixed with 50 parts water to prepare a 50 wt % aqueous solution (SD).
- Preparation of emulsions of polydiorganosiloxanes (E) through (H). 300 Parts of the polydiorganosiloxane (E) obtained in Synthesis Example 5 were emulsified and dispersed in 260 parts water in a homomixer using 40 parts polyoxyethylene (6 mol) lauryl ether as the nonionic surfactant, so as to prepare an emulsion (EE) containing 50 wt % polydiorganosiloxane. 300 Parts of the polydiorganosiloxane (F) obtained in Synthesis Example 6 were emulsified and dispersed in 260 parts water in a homomixer using 40 parts polyoxyethylene (6 mol) lauryl ether as the nonionic surfactant, so as to prepare an emulsion (EF) containing 50 wt % polydiorganosiloxane. 300 Parts of the polydiorganosiloxane (G) obtained in Synthesis Example 7 were emulsified and dispersed in 260 parts water in a homomixer using 40 parts polyoxyethylene (6 mol) lauryl ether as the nonionic surfactant, so as to prepare an emulsion (EG) containing 50 wt % polydiorganosiloxane. 300 Parts of the polydiorganosiloxane (H) obtained in Synthesis Example 8 was emulsified and dispersed in 260 parts water in a homomixer using 40 parts polyoxyethylene (6 mol) lauryl ether as the nonionic surfactant, so as to prepare an emulsion (EH) containing 50 wt % polydiorganosiloxane.
- The aqueous solutions and emulsions obtained in Synthesis Examples 9 and 10 were blended in the amounts given in Table 1 to prepare synthetic fiber treatment agents. The resulting treatment agents were sprayed onto polyester staple fibers (6 d, 65 mm long) for mattress padding so that a total amount of 0.5 wt % polyorganosiloxane adhered to the fibers, and the material was dried at room temperature, followed by 5 minutes of heat treatment at 150° C. The treated polyester mattress padding was carded with a Labromixer (Textest) and superposed to prepare padding for evaluation. The resulting padding was manually assessed for smoothness and repulsion according to the following criteria. The amount of methanol contained in the resulting synthetic fiber treatment agent compositions (theoretical amount) was calculated by the following formula. The results are given in Table 1.
- Smoothness
- *: downy-like hand, with ample smoothness
- O: smooth hand
- Δ: somewhat coarse, with a hand characterized by somewhat inferior smoothness
-
- The emulsions and aqueous solutions obtained in Synthesis Examples 9 and 10 were used to prepare synthetic fiber treatment agents using the amounts shown in Table 1. The resulting treatment agents were used to treat polyester staple fibers for mattress padding in the same manner as in Example 1, and the material was carded to produce mattress padding. The resulting padding was assessed for smoothness, repulsion, and methanol content in the same manner as in Example 1. The results are given in Table 1.
- N-β-(aminoethyl)-γ-aminopropylmethyldimethoxysilane was added in the amounts shown in Table 1 to the emulsions EE and EH obtained in Synthesis Example 10 to prepare synthetic fiber treatment agents. The resulting treatment agents were used to treat polyester staple fibers for mattress padding in the same manner as in Example 1, and the material was carded to produce mattress padding. The resulting padding was assessed for smoothness, repulsion, and methanol content in the same manner as in Example 1. The results are given in Table 1.
TABLE 1 Methanol Blended composition (weight parts) content Component (A) Component (B) aminosilane Evaluation (%, SA SB SC SD EE EF EG EH *1 smoothness repulsion theoretical) Example 1 8 — — — 100 — — — — * O 0 Example 2 2 — — — 100 — — — — O O 0 Example 3 30 — — — 100 — — — — * O 0 Example 4 — 10 — — 100 — — — — * O 0 Example 5 — 20 — 100 — — — — * O 0 Example 6 — 10 — — — 100 — — — * O 0.10 Example 7 — 6 — — — — 100 — — O O 0 Example 8 20 — — — — — 100 — * O 0 Example 9 — 10 — — — 50 — 50 — * O 0.05 Comp. Ex. — — — — 100 — — — — Δ X 0 1 Comp. Ex. — — — — — 100 — — — Δ X 0.11 2 Comp. Ex. — — — — — — 100 — — Δ Δ 0 3 Comp. Ex. — — — — — — — 100 — X X 0 4 Comp. Ex. — — — 20 100 — — — — O O 1.46 5 Comp. Ex. — — — — 100 — — — 10 * O 2.82 6 Comp. Ex. — — — — — — — 100 20 O O 5.18 7
Claims (16)
1. A synthetic fiber treatment agent composition comprising
(A) an amino group-containing polyorganosiloxane, where the terminals of the molecular chain are groups described by general formula
where R is a C1 to C20 optionally substitutable monovalent hydrocarbon or hydroxyl group, with at least 80 mol % of all the R comprising monovalent hydrocarbon groups; R2 is a C1 to C10 divalent hydrocarbon group; R3 and R4 are hydrogen atoms or C1 to C20 optionally substitutable monovalent hydrocarbon groups; a is an integer from 0 to 5; p is an integer from 0 to 2; q is an integer from 0 to 3, and r is 0 or 1, where (p+q+r)=3, and at least 30 mol % of all siloxane units per molecule are amino group-containing diorganosiloxane units described by general formula
where R, R2, R3, R4, and a are the same as above and
(B) a polydiorganosiloxane described by general formula
where A is selected from a group consisting of trialkylsilyl group, hydrogen atom, and C1 to C20 optionally substitutable monovalent hydrocarbon groups; R, R2, R3, R4, and a are the same as above; x is an integer of 1 or more; and y is 0 or an integer of 1 or more, where y/(x+y) is no more than 0.1.
2. A synthetic fiber treatment agent composition according to claim 1 , where A in component (B) is a hydrogen atom or C1 to C20 alkyl group.
3. A synthetic fiber treatment agent composition according to claim 1 , where component (B) is a mixture of a polydiorganosiloxane in which y is 0, and an amino group-containing polydiorganosiloxane in which y is an integer of 1 or more.
4. A synthetic fiber padding treated with the synthetic fiber treatment agent composition of claim 1 .
5. A synthetic fiber padding treated with the synthetic fiber treatment agent composition of claim 2 .
6. A synthetic fiber padding treated with the synthetic fiber treatment agent composition of claim 3 .
7. A synthetic fiber treatment agent composition according to claim 1 , where a is an integer of 0 or 1.
8. A synthetic fiber treatment agent composition according to claim 1 , where the content of the amino group-containing diorganosiloxane units in component (A) is at least 50 mol %.
9. A synthetic fiber treatment agent composition according to claim 1 , where the content of the amino group-containing diorganosiloxane units in component (A) is at least 70 mol %.
10. A synthetic fiber treatment agent composition according to claim 1 , where component (A) as a degree of polymerization of 10 to 500.
11. A synthetic fiber treatment agent composition according to claim 1 , where component (B) as a viscosity at 25° C. of 300 to 30,000 mm2/s.
12. A synthetic fiber treatment agent composition according to claim 1 , where in component (B) the ratio of y/(x+y) is no more than 0.02.
13. A synthetic fiber treatment agent composition according to claim 1 comprising 1 to 50 weight parts of component (B) per 100 weight parts of component (A).
14. A synthetic fiber treatment agent composition according to claim 1 comprising 2 to 30 weight parts of component (B) per 100 weight parts of component (A).
15. A synthetic fiber treatment agent composition according to claim 1 further comprising a solvent as a diluent.
16. A synthetic fiber treatment agent composition according to claim 1 , where the composition is an emulsion.
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JP2000161803A JP4597316B2 (en) | 2000-05-31 | 2000-05-31 | Synthetic fiber treatment agent composition |
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EP (1) | EP1160372A1 (en) |
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Cited By (3)
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US20060015556A1 (en) * | 2004-07-02 | 2006-01-19 | Pounds Gregory E | Method and apparatus for cordless phone and other telecommunications services |
US20070039103A1 (en) * | 2005-08-17 | 2007-02-22 | The Procter & Gamble Company | Fiber and hair fiber conditioning treatment composition |
US20080275205A1 (en) * | 2007-05-02 | 2008-11-06 | Wacker Chemie Ag | Process For Preparing Aminoalkylpolysiloxanes |
Families Citing this family (7)
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GB0209134D0 (en) * | 2002-04-22 | 2002-05-29 | Procter & Gamble | Silicones |
EP1661873A1 (en) * | 2004-11-24 | 2006-05-31 | Danish Technological Institute, Materials, Materials Testing | Anti-graffiti coating |
DE102005011112A1 (en) * | 2005-03-10 | 2006-09-14 | Holmenkol Sport-Technologies Gmbh & Co. Kg | Process for improving the surface smoothness of textile fabrics |
WO2007021604A2 (en) * | 2005-08-17 | 2007-02-22 | The Procter & Gamble Company | A fiber and hair fiber conditioning treatment composition |
DE102007020568A1 (en) * | 2007-05-02 | 2008-11-06 | Wacker Chemie Ag | Process for the continuous preparation of aminoalkyl-containing organopolysiloxanes |
CN103422356A (en) * | 2012-05-23 | 2013-12-04 | 台嘉玻璃纤维有限公司 | Electronic grade glass fiber cloth surface treating agent and method for producing glass fiber cloth |
JP7003707B2 (en) * | 2018-02-07 | 2022-01-21 | 信越化学工業株式会社 | Fiber treatment agent and its manufacturing method |
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DE2436741A1 (en) | 1974-07-30 | 1976-02-12 | Bayer Ag | METHOD FOR PREPARING MODIFIED POLYISOCYANATE |
JPS5319715A (en) | 1976-08-06 | 1978-02-23 | Matsushita Electric Ind Co Ltd | Becgh |
JPS594918B2 (en) | 1976-08-06 | 1984-02-01 | 松下電器産業株式会社 | Recording and reproducing method of PAL color television signal |
US4247592A (en) * | 1980-03-12 | 1981-01-27 | Dow Corning Corporation | Method for treating synthetic textiles with aminoalkyl-containing polydiorganosiloxanes |
JPS581231A (en) | 1981-06-26 | 1983-01-06 | Toshiba Corp | Key input circuit |
JPS5817310A (en) | 1981-07-23 | 1983-02-01 | Furukawa Electric Co Ltd:The | Method for measuring nonmagnetic long material |
JPH066680B2 (en) * | 1985-10-30 | 1994-01-26 | 東レ・ダウコーニング・シリコーン株式会社 | Primer composition |
JPS6375184A (en) * | 1986-09-19 | 1988-04-05 | 信越化学工業株式会社 | Treatment agent for synthetic fiber |
JPH01221580A (en) * | 1988-02-27 | 1989-09-05 | Shin Etsu Chem Co Ltd | Textile treating agent |
US5063260A (en) * | 1991-05-01 | 1991-11-05 | Dow Corning Corporation | Compositions and their use for treating fibers |
DE4217561A1 (en) * | 1992-05-27 | 1993-12-02 | Wacker Chemie Gmbh | Aqueous dispersions of organopolysiloxanes |
JPH07119043A (en) * | 1993-10-27 | 1995-05-09 | Toray Dow Corning Silicone Co Ltd | Method for exhaustion treatment of fiber |
JPH07305278A (en) | 1994-05-11 | 1995-11-21 | Shin Etsu Chem Co Ltd | Treating agent for synthetic fiber |
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US20060015556A1 (en) * | 2004-07-02 | 2006-01-19 | Pounds Gregory E | Method and apparatus for cordless phone and other telecommunications services |
US20070039103A1 (en) * | 2005-08-17 | 2007-02-22 | The Procter & Gamble Company | Fiber and hair fiber conditioning treatment composition |
US20080275205A1 (en) * | 2007-05-02 | 2008-11-06 | Wacker Chemie Ag | Process For Preparing Aminoalkylpolysiloxanes |
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TWI238868B (en) | 2005-09-01 |
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US6441105B2 (en) | 2002-08-27 |
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CN1249293C (en) | 2006-04-05 |
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