US2785145A - Siliconate-aminoplast compositions and textiles coated therewith - Google Patents
Siliconate-aminoplast compositions and textiles coated therewith Download PDFInfo
- Publication number
- US2785145A US2785145A US440848A US44084854A US2785145A US 2785145 A US2785145 A US 2785145A US 440848 A US440848 A US 440848A US 44084854 A US44084854 A US 44084854A US 2785145 A US2785145 A US 2785145A
- Authority
- US
- United States
- Prior art keywords
- water
- siliconate
- soluble
- textile
- aminoplast
- 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
- 239000000203 mixture Substances 0.000 title claims description 33
- 229920003180 amino resin Polymers 0.000 title claims description 19
- 239000004753 textile Substances 0.000 title description 32
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 15
- 229920000877 Melamine resin Polymers 0.000 claims description 12
- 150000003839 salts Chemical class 0.000 claims description 11
- 239000007864 aqueous solution Substances 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 6
- 239000004202 carbamide Substances 0.000 claims description 6
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 claims description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 229920001187 thermosetting polymer Polymers 0.000 claims description 4
- 150000005215 alkyl ethers Chemical class 0.000 claims description 3
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 claims description 3
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 claims description 3
- 239000000463 material Substances 0.000 description 38
- 239000004744 fabric Substances 0.000 description 19
- 125000005625 siliconate group Chemical group 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 238000000034 method Methods 0.000 description 15
- 230000008569 process Effects 0.000 description 13
- 239000005871 repellent Substances 0.000 description 13
- 239000002657 fibrous material Substances 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- GBPOWOIWSYUZMH-UHFFFAOYSA-N sodium;trihydroxy(methyl)silane Chemical compound [Na+].C[Si](O)(O)O GBPOWOIWSYUZMH-UHFFFAOYSA-N 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 238000005108 dry cleaning Methods 0.000 description 7
- -1 polysiloxanes Polymers 0.000 description 7
- 230000002940 repellent Effects 0.000 description 7
- 229920000742 Cotton Polymers 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- 235000013877 carbamide Nutrition 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical class OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 3
- 238000004900 laundering Methods 0.000 description 3
- ZJBHFQKJEBGFNL-UHFFFAOYSA-N methylsilanetriol Chemical compound C[Si](O)(O)O ZJBHFQKJEBGFNL-UHFFFAOYSA-N 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229940089952 silanetriol Drugs 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- GJMPSRSMBJLKKB-UHFFFAOYSA-N 3-methylphenylacetic acid Chemical class CC1=CC=CC(CC(O)=O)=C1 GJMPSRSMBJLKKB-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical class NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 238000009988 textile finishing Methods 0.000 description 2
- 229940117957 triethanolamine hydrochloride Drugs 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- 101100348017 Drosophila melanogaster Nazo gene Proteins 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
- 241000208202 Linaceae Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- VGGLHLAESQEWCR-UHFFFAOYSA-N N-(hydroxymethyl)urea Chemical compound NC(=O)NCO VGGLHLAESQEWCR-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Chemical class 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical class N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 150000005840 aryl radicals Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical class [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- WVJOGYWFVNTSAU-UHFFFAOYSA-N dimethylol ethylene urea Chemical compound OCN1CCN(CO)C1=O WVJOGYWFVNTSAU-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 239000005052 trichlorosilane Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
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
- 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
-
- 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
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
-
- 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
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/01—Silicones
-
- 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
- Y10T442/2164—Coating or impregnation specified as water repellent
- Y10T442/2197—Nitrogen containing
Definitions
- This invention relates to mixtures of water-soluble salts of substituted silanetriols and water-soluble aminoplast resins and also to the treatment of fibrous materials therewith.
- An object of the invention is to provide an improved composition for imparting water repellent characteristics to fibrous materials.
- Another object of the invention is to provide an improved process for imparting a water-repellent finish to fibrous materials.
- a further object of the invention is to provide improved water repellent textile materials.
- fibrous materials may be treated with a mixture of a water-soluble siliconate in admixture with a water-soluble amino resin followed by drying and curing the impregnated material on conventional equipment according to standard operating procedures used in 4 commercial textile finishing plants to impart a water repellent finish of a relatively permanent nature, that is, one which is durable to both prolonged laundering or repeated dry cleaning operations. N involved treatments or special curing conditions are required in the process and no reduction in the usual production rate is necessary.
- the treated material has the characteristics such as shrink resistance, crease resistance, etc. which are imparted by treatment with the aminoplast alone.
- the invention accordingly comprises a composition containing an aqueous solution of a water-soluble metal salt of a hydrocarbon silanetriol and a water-soluble thermo-setting aminoplast, the treatment of fibrous materials with said solutions followed by treating the heated material to dry and cure said composition to the substantially water-insoluble state and also the resulting product.
- siliconates of the type contemplated in the present invention ofier many advantages over the siloxane polymers which have been used for rendering textile materials ice water repellent.
- the various polysiloxanes are all irisoluble in Water and the textile finisher must either apply them to cloth in the form of organic solvent solutions with the attendant fire and/or health hazards, greater cost and a larger capital outlay for solvent recovery equipment or he must employ aqueous emulsions which have to be made up with special emulsifying equipment such as colloid mills, homogeuizers, etc. in order to use the conventional water medium of the textile industry.
- the siliconates operative with the present invention are strong bases. They are the water-soluble hydrocarbon-substituted metal siliconates or metal salts of hydrocarbon-substituted silanetriols which may be prepared as described in Patent 2,507,200 by hydrolyzing an alkyl or aryl trichlorosilane in ice water, filtering off the precipitate and adding an equimolar amount of aqueous sodium hydroxide or another base to produce a solution of an essentially monomeric material having the probable formula:
- R is an alkyl, cycloalkyl or aryl radical having a suificiently small number of carbon atoms to provide substantial solubility of the compound in water; for example, R may be a methyl, ethyl, isopropyl, cyclopropyl, phenyl or like hydrocarbon radical.
- the preferred substituents are lower alkyl radicals and the best results appear to be obtained with sodium methyl siliconate.
- a broad variety of heat-reactive, water-soluble resinforming aminoplasts may be employed in the present invention. These include the various polymethylol melamines, particularly diand trimethylol melamines, monoand dimethylol ureas, lower alkyl others of'the aforesaid melamine and urea compounds (for example, methylated methylol melamines and methylated'methylol ureas) monoand dimethylol ethylene urea and mixtures M represents are greatly preferred, and especially the ethers thereof,
- a conventional curing agent for thermosetting amino resins should be present when the impregnated fabric is cured.
- the catalyst or accelerator is desirably added to the treating bath in order to simplify operations and this agent should be of a type which is compatible with any ingredient, in the alkaline treating bath.
- these catalysts are ammonium sulfate, diammonium hydrogen phosphate, triethanolamine hydrochloride, ammonium chloride and acid salts of amines such as the hydrochloride salts of Z-methyl, Z-amino propanol-l or mixed isopropanolamines.
- the optimum quantity of accelerator will, of course, vary somewhat with the substance selected but, in general, about 1 to about 30 percent of catalyst, based on the total weight of the amino resin solids in the impregnating bath should be used and the preferred range is from about 3 to about 20 percent.
- a wide variety of textile treating additives may be incorporated in pad baths prepared according to the present invention.
- softening agents may be added to produce a softer hand or feel in the finished material. It is not thought that this will often be necessary because the hand of the finished material can also be determined by the choice of an aminoplast resin from the broad variety indicated above and by regulating the pick-up of amino resin on the textile fabric.
- Odor preventatives may be mixed into the present compositions as exemplified by small amounts of urea or dicyandiamide which function to take up any formaldehyde released in the pad bath or in the curing operation.
- salts of diorganosilanediols and a strong base such as those disclosed above in connection with the siliconate component may also be added to the aqueous solution. These may be prepared in the manner disclosed in U. S. Patent 2,507,200. Quantities of these siliconate modifiers may range in relative molar proportions between about 1 and about 9 mols of the siliconate per mol of soluble siliconate. Of the modifiers, sodium dimethyl siliconate is preferred.
- the treatment described herein is applicable to any woven, knitted or felted textile material.
- This includes fabrics made up in whole or in part of the fibers of cotton, viscose rayon, cuprammonium rayon, cellulose acetate, wool, silk, flax, nylon of both the adipamide and caprolactam types, homoand copolymers of acrylonitrile, polyesters such as polyethyleneglycol terephthalate, and so forth.
- the figure represents in plan view a textile fabric impregnated with the heatcured reaction product of one of the aforesaid siliconates and an aminoplast of the type described hereinabove.
- a pad bath In treating textile materials, a pad bath is the most convenient means of uniformly impregnating a textile add-on.
- the expressions bearing and impregnated are used herein to include either deposits of the agent in the interior of the fibers or on the surface of the fibers or both.
- the treated fabric may be dried and cured in two separate operations.
- the material is dried in equipment operating at a temperature of at least 180 F.
- the drying and curing is performed in equipment operating at temperatures ranging between 180 F. and the point at which deterioration of the fibrous materials begins. In general, this operation may be conducted at temperatures between about 200 and about 500 F. for a period ranging between about 10 seconds and 30 minutes with the time of cure decreasing as the temperature is increased.
- the optimum drying and curing is obtained by exposure to temperatures between 250 and 400 F. for a period between 30 seconds and 15 minutes.
- Example 1 Bleached, unmercerized cotton poplin having an x 80 count is padded through an aqueous solution containing 4.4% of sodium methyl siliconate with the squeeze rolls adjusted for a wet pick-up of of the fabric weight.
- the impregnated-material is then dried at 225 F.
- One sample of the treated percale is exposed to a temperature of 350 F. for 5 minutes while another sample is similarly heated for 15 minutes. Both samples are then subjected to a conventional process wash in an aqueous solution of 0.1% soap and 0.1% sodium carbonate.
- three swatches of cloth are cut from each sample.
- One of these swatches is subjected to three dry cleaning operations in Varsol No. 2 solvent for 20 minutes in a tumbling jar rotating at 55 R. P. M.
- Another swatch is subjected to a Sanforize Wash according to the Standard Test Method 14-52 (page 132). of the 1952 Technical Manual and Year Book of the American Association of Technical Chemists and Colorists;
- the samples of treated fabric show no improvement in water repellency over the untreated cotton cloth initially after curing for both 5 and 15 minutes at the stated temperature and also after being subjected to the aforesaid washing and dry cleaning operations. It is accordingly apparent that the treatment of fabrics with sodium methyl siliconate is ineffective in producing any improvement in Water repellency whenaccelerated drying is employed.
- Example 2 The procedure of Example 1 is repeated using an aque ous pad bath containing 3.9% by weight sodium methyl siliconate, methylated trimethylcl melamine in essentially monomeric form, 1% triethanolamine hydrochloride as a catalyst for the melamine resin and 0.5% urea as an odor preventive. After drying at 225 F. the treated 80 x 80 cotton percale is divided into samples which are cured at 350 F. for 5 and minutes respectively and then subjected to the same process wash. Both samples display good water repellency and spot resistance. In addition, excellent shrink resistance and crease resistance, as well as a good hand are observed. A swatch from each sample is subjected to a Sanforize wash.
- Example 3 Example 1 is again substantially duplicated using an aqueous pad bath containing 3.9% by weight sodium methyl siliconate, 15% of an essentially monomeric con densate of urea and formaldehyde in a-1:1.33 molar ratio, and 1% triethanolam'ine hydrochloride as a catalyst.- After drying at 225 F. the treated 80 x 80 cotton percale is divided into samples which are cured at 350 F. for 5 and 15 minutes respectively and then subjected to the same process wash. Both samples display good water repellency and spot resistance. In addition, excellent shrink resistance and crease resistance, as well as a good hand are observed. A swatch from each sample is subjected to a Sanforize wash.
- a composition of matter which comprises an aqueous solution of a water-soluble metal salt of a hydrocarbon silanetriol and a water-soluble thermosetting aminoplast of the group consisting of formaldehyde con densates of melamine, urea, ethyleneurea, succinamide, adipamide, alkyl ethers of said condensates and polymers thereof.
- a composition of matter which comprises an aqueous solution of a water-soluble metal salt of a hydrocarbon silanetriol, a water-soluble thermosetting mind plast of the group consisting of formaldehyde condensates of melamine, urea, ethyleneurea, succinamide, adipamide, alkyl ethers of said condensates and polymers thereof and a curing catalyst for the aminoplast.
- a composition of matter which comprises an aqueous solution of a water-soluble alkali metal lower alkyl siliconate, a water-soluble melamine-formaldehyde condensate and a curing catalyst for the melamine-formaldehyde condensate.
- composition according to claim 3 in which the melamine-formaldehyde condensate comprises methylated trirnethylol melamine.
- a composition of matter which comprises an aqueous solution of parts by weight of sodium methyl siliconate, between about 25 and about 1000 parts of methylated trimethylol melamine and a sufficient quantity of a curing catalyst to cure the methylated trimethylol melamine to the water-insoluble state.
- a process which comprises contacting a textile material with a composition according to claim 1 and heating the treated material to dry and cure said composition to the substantially water-insoluble'state, whereby a durable water-repellent finish is imparted to the textile material.
- a process which comprises contacting a textile material with a composition according to claim 2 and heating the treated material to dry and cure said composition to the substantially water-insoluble state, whereby a durable water-repellent finish is imparted to the textile material.
- a process which comprises contacting a textile material with a composition according to claim 3 and heating the treated material to dry and cure said composition to the substantially water-insoluble state, whereby a durable water-re ellent finish is imparted to the textile material.
- a process which contacting a textile material with a composition according to claim 4 and heating the treated m terial to dry and cure said composition to the substantially water-insoluble state, whereby a durable water-repellent finish is imparted to the textile material.
- a process which comprises contacting a textile material with a composition according to claim 5 in sufiicient quantity to deposit a total of at least 2 percent of said siliconate and melamine resin thereon based on the weight of the dry textile material and heating the treated material to a temperature of at least degrees Fahrenheit for a period sufiicient to dry and cure said composition to the substantially water-insoluble state, whereby a durable water-repellent finish is imparted to the textile material.
- An article which comprises a textile material impregnated with the heat-cured reaction product of a composition according to claim 1.
- An article which comprises a textile material impregnated with the heat-cured reaction product of a composition according to claim 2.
- An article which comprises a textile material impregnated with the heat-cured reaction product of a composition according to claim 4.
- a textile article having a durable water-repellent finish which comprises a textile material impregnated with at least 2 percent by weight of the heat-cured reaction product of a composition according to claim 5.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
March 1 57 T. F. COOKE ETA]. 2,785,145
SILICONATE-AMINOPLAST COMPOSITIONS AND TEXTILES COATED THEREWITH Flled July 1, 1954 mum .OUO ROLR mcF N u M/W wm ML T W A T TORNE Y.
United States atent SlLICONATE-AMINOPLAST COMPGSITIONS AND TEXTILES CDATED THEREWITH Theodore F. Cooke, Martinsviiie, Linton A. Flock,
Pluckemin, and Philip B. Roth, Somerville, N. 3., assignors to American Cyanamid Company, New York, N. Y., a corporation of Maine Application duly 1, 1954-, Serial No. 440,848
15 Claims. (Cl. 269-29.4)
This invention relates to mixtures of water-soluble salts of substituted silanetriols and water-soluble aminoplast resins and also to the treatment of fibrous materials therewith.
When textile materials are impregnated with a solution of sodium methyl siliconate or other water-soluble salts Y of substituted silanetriols a water repellent finish is obtained after prolonged drying in air. However this treatment is not commercially feasible since, few, if any, textile finishing plants operate at such low production rates or have sufiicient storage areas available for long air drying operations. When the impregnated fabric is dried rapidly by heating on conventional equipment such as tenter frames, or large drying rolls or cans, followed by the usual process Wash, the finished fabric is not water repellent. In U. S. Patent 2,507,200 it is suggested that a water repellent finish can be obtained by curing cloth impregnated with water-soluble siliconates under acidic conditions. This, of course, complicates the process.
An object of the invention is to provide an improved composition for imparting water repellent characteristics to fibrous materials.
Another object of the invention is to provide an improved process for imparting a water-repellent finish to fibrous materials.
A further object of the invention is to provide improved water repellent textile materials.
Other objects and advantages of the invention will be apparent to those skilled in the art especially upon consideration of the detailed disclosure hereinbelow.
It has been found that fibrous materials may be treated with a mixture of a water-soluble siliconate in admixture with a water-soluble amino resin followed by drying and curing the impregnated material on conventional equipment according to standard operating procedures used in 4 commercial textile finishing plants to impart a water repellent finish of a relatively permanent nature, that is, one which is durable to both prolonged laundering or repeated dry cleaning operations. N involved treatments or special curing conditions are required in the process and no reduction in the usual production rate is necessary. In addition to water repellency, the treated material has the characteristics such as shrink resistance, crease resistance, etc. which are imparted by treatment with the aminoplast alone.
The invention accordingly comprises a composition containing an aqueous solution of a water-soluble metal salt of a hydrocarbon silanetriol and a water-soluble thermo-setting aminoplast, the treatment of fibrous materials with said solutions followed by treating the heated material to dry and cure said composition to the substantially water-insoluble state and also the resulting product.
siliconates of the type contemplated in the present invention ofier many advantages over the siloxane polymers which have been used for rendering textile materials ice water repellent. The various polysiloxanes are all irisoluble in Water and the textile finisher must either apply them to cloth in the form of organic solvent solutions with the attendant fire and/or health hazards, greater cost and a larger capital outlay for solvent recovery equipment or he must employ aqueous emulsions which have to be made up with special emulsifying equipment such as colloid mills, homogeuizers, etc. in order to use the conventional water medium of the textile industry. Even then the methyl hydrogen polysiloxane which is a component of many such emulsions introduces difiiculties by reason of its tendency to evolve gaseous hydrogen which complicates packaging and storing the emulsions. No such difiiculties are encountered with the siliconates by reason of their ready solubility in even cold water. However, the siliconates pose a problem, which is not typical of the application of silicone resins to cloth, in that they do not cure on the fabric in a reasonable time at elevated temperatures.
The siliconates operative with the present invention are strong bases. They are the water-soluble hydrocarbon-substituted metal siliconates or metal salts of hydrocarbon-substituted silanetriols which may be prepared as described in Patent 2,507,200 by hydrolyzing an alkyl or aryl trichlorosilane in ice water, filtering off the precipitate and adding an equimolar amount of aqueous sodium hydroxide or another base to produce a solution of an essentially monomeric material having the probable formula:
OH R-SP-OM H in dilute aqueous solution and the following probable formula:
when dried to a solid. In this formulae, R is an alkyl, cycloalkyl or aryl radical having a suificiently small number of carbon atoms to provide substantial solubility of the compound in water; for example, R may be a methyl, ethyl, isopropyl, cyclopropyl, phenyl or like hydrocarbon radical. The preferred substituents are lower alkyl radicals and the best results appear to be obtained with sodium methyl siliconate. an atom of an alkali metal or an alkaline earth metal including sodium, potassium, lithium, barium, calcium and strontium. in the case of the latter three polyvalent metals, two of the siliconate radicals are bonded to the metal atom. While it is contemplated that other metal ions may be present by the addition of soluble salts such as lead, zinc, silver and copper to the siliconate of a strong base with probable formation of complex metalosiliconates, it does not appear that any advantages areobtained by this addition. Although the presence of copper ions may produce resistance to mildew and other fungi, aminoplasts of the type described below produce fungicidal properties in fibrous materials and it does not seem that anything is gained by the further addition of a copper salt. Moreover, salts of these other metals may impair the solubility of the siliconate of a strong base.
A broad variety of heat-reactive, water-soluble resinforming aminoplasts may be employed in the present invention. These include the various polymethylol melamines, particularly diand trimethylol melamines, monoand dimethylol ureas, lower alkyl others of'the aforesaid melamine and urea compounds (for example, methylated methylol melamines and methylated'methylol ureas) monoand dimethylol ethylene urea and mixtures M represents are greatly preferred, and especially the ethers thereof,
for outstanding results have been obtained with the methylated methylol melamine mixture which approximates the dimethyl ether of trimethylol melamine. These and the other resins listed above are prepared by methods known to those skilled in the art and which accordingly need not be set forth here.
In order to accelerate the curing of the resin-forming mixture to a degree feasible for use in commercial finishing plants, a conventional curing agent for thermosetting amino resins should be present when the impregnated fabric is cured. The catalyst or accelerator is desirably added to the treating bath in order to simplify operations and this agent should be of a type which is compatible with any ingredient, in the alkaline treating bath. Among the many such catalysts are ammonium sulfate, diammonium hydrogen phosphate, triethanolamine hydrochloride, ammonium chloride and acid salts of amines such as the hydrochloride salts of Z-methyl, Z-amino propanol-l or mixed isopropanolamines. The optimum quantity of accelerator will, of course, vary somewhat with the substance selected but, in general, about 1 to about 30 percent of catalyst, based on the total weight of the amino resin solids in the impregnating bath should be used and the preferred range is from about 3 to about 20 percent.
If desired a wide variety of textile treating additives may be incorporated in pad baths prepared according to the present invention. For example, softening agents may be added to produce a softer hand or feel in the finished material. It is not thought that this will often be necessary because the hand of the finished material can also be determined by the choice of an aminoplast resin from the broad variety indicated above and by regulating the pick-up of amino resin on the textile fabric. Odor preventatives may be mixed into the present compositions as exemplified by small amounts of urea or dicyandiamide which function to take up any formaldehyde released in the pad bath or in the curing operation.
Where a softer texture of the treated material is desired salts of diorganosilanediols and a strong base such as those disclosed above in connection with the siliconate component may also be added to the aqueous solution. These may be prepared in the manner disclosed in U. S. Patent 2,507,200. Quantities of these siliconate modifiers may range in relative molar proportions between about 1 and about 9 mols of the siliconate per mol of soluble siliconate. Of the modifiers, sodium dimethyl siliconate is preferred.
While well adapted to the treatment of cotton fabrics, the treatment described herein is applicable to any woven, knitted or felted textile material. This includes fabrics made up in whole or in part of the fibers of cotton, viscose rayon, cuprammonium rayon, cellulose acetate, wool, silk, flax, nylon of both the adipamide and caprolactam types, homoand copolymers of acrylonitrile, polyesters such as polyethyleneglycol terephthalate, and so forth.
In the accompanying drawing the figure represents in plan view a textile fabric impregnated with the heatcured reaction product of one of the aforesaid siliconates and an aminoplast of the type described hereinabove.
In treating textile materials, a pad bath is the most convenient means of uniformly impregnating a textile add-on.
material. However, sprays and other suitable means of applying the solution are also contemplated. Considerable latitude may be exercised in selecting the particular concentration of solids in the pad bath. For most pur poses a bath containing between about 2 and about 40 percent of solids is recommended. The adjustment of the squeeze rolls is correlated with the pad bath concentration in the usual manner to provide the desired With the novel compositions these factors should be adjusted to provide an add-on or impregnation of the textile material of at least 2 percent of the soluble siliconate and aminoplast based on the weight of the dry fibrous material. The optimum pick-up of amino resin and siliconate is between 5 and 15 percent of the untreated fabric Weight. While it is contemplated that larger quantities may be employed, little or nothing appears to be gained by depositing more than 40 percent on the cloth.
It is not known with certainty whether the new agents penetrate into the interior of individual fibers or remain on their surface. Accordingly, the expressions bearing and impregnated are used herein to include either deposits of the agent in the interior of the fibers or on the surface of the fibers or both.
The treated fabric may be dried and cured in two separate operations. In this case the material is dried in equipment operating at a temperature of at least 180 F. However, it is usually preferable to dry and cure in a single operation in order to simplify the process curing alone or combined. The drying and curing is performed in equipment operating at temperatures ranging between 180 F. and the point at which deterioration of the fibrous materials begins. In general, this operation may be conducted at temperatures between about 200 and about 500 F. for a period ranging between about 10 seconds and 30 minutes with the time of cure decreasing as the temperature is increased. For. most fibrous materials the optimum drying and curing is obtained by exposure to temperatures between 250 and 400 F. for a period between 30 seconds and 15 minutes.
For a better understandingof the nature and objects of this invention, reference should be had to the accompanying examples in which all proportions are set forth in terms of weight unless otherwise indicated.
Example 1' Bleached, unmercerized cotton poplin having an x 80 count is padded through an aqueous solution containing 4.4% of sodium methyl siliconate with the squeeze rolls adjusted for a wet pick-up of of the fabric weight. The impregnated-material is then dried at 225 F. One sample of the treated percale is exposed to a temperature of 350 F. for 5 minutes while another sample is similarly heated for 15 minutes. Both samples are then subjected to a conventional process wash in an aqueous solution of 0.1% soap and 0.1% sodium carbonate. Then three swatches of cloth are cut from each sample. One of these swatches is subjected to three dry cleaning operations in Varsol No. 2 solvent for 20 minutes in a tumbling jar rotating at 55 R. P. M. Another swatch is subjected to a Sanforize Wash according to the Standard Test Method 14-52 (page 132). of the 1952 Technical Manual and Year Book of the American Association of Technical Chemists and Colorists;
Upon making Water repellency determinations, the samples of treated fabric show no improvement in water repellency over the untreated cotton cloth initially after curing for both 5 and 15 minutes at the stated temperature and also after being subjected to the aforesaid washing and dry cleaning operations. It is accordingly apparent that the treatment of fabrics with sodium methyl siliconate is ineffective in producing any improvement in Water repellency whenaccelerated drying is employed.
sodium methyl siliconate solution containing 16.5 percent :0.5 percent total base titrated as NazO and 35.5 percent percent total silicone calculated as CH3SiO1.5.
Example 2 The procedure of Example 1 is repeated using an aque ous pad bath containing 3.9% by weight sodium methyl siliconate, methylated trimethylcl melamine in essentially monomeric form, 1% triethanolamine hydrochloride as a catalyst for the melamine resin and 0.5% urea as an odor preventive. After drying at 225 F. the treated 80 x 80 cotton percale is divided into samples which are cured at 350 F. for 5 and minutes respectively and then subjected to the same process wash. Both samples display good water repellency and spot resistance. In addition, excellent shrink resistance and crease resistance, as well as a good hand are observed. A swatch from each sample is subjected to a Sanforize wash. In addition another swatch of each sample is subjected to three successive dry cleaning operations in Varsol solvent. It is found that both dry-cleaned swatches and both washed swatches have the same spray ratings as before the dry cleaning and laundering operations and that the other desirable qualities of the treated material are substantially fully retained.
Example 3 Example 1 is again substantially duplicated using an aqueous pad bath containing 3.9% by weight sodium methyl siliconate, 15% of an essentially monomeric con densate of urea and formaldehyde in a-1:1.33 molar ratio, and 1% triethanolam'ine hydrochloride as a catalyst.- After drying at 225 F. the treated 80 x 80 cotton percale is divided into samples which are cured at 350 F. for 5 and 15 minutes respectively and then subjected to the same process wash. Both samples display good water repellency and spot resistance. In addition, excellent shrink resistance and crease resistance, as well as a good hand are observed. A swatch from each sample is subjected to a Sanforize wash. In addition another swatch of each sample is subjected to three successive dry cleaning operations in Varsol solvent. It is found that both dry-cleaned swatches and both washed swatches have the same spray ratings as before the dry cleaning and laundering operations and that the other desirable qualities of the treated material are substantially fully retained.
The above examples are included to illustrate the invention and it is to be understood that the present invention is not limited thereto since various modifications and alterations may be made without departing from the scope of this invention.
We claim:
1. A composition of matter which comprises an aqueous solution of a water-soluble metal salt of a hydrocarbon silanetriol and a water-soluble thermosetting aminoplast of the group consisting of formaldehyde con densates of melamine, urea, ethyleneurea, succinamide, adipamide, alkyl ethers of said condensates and polymers thereof.
2. A composition of matter which comprises an aqueous solution of a water-soluble metal salt of a hydrocarbon silanetriol, a water-soluble thermosetting mind plast of the group consisting of formaldehyde condensates of melamine, urea, ethyleneurea, succinamide, adipamide, alkyl ethers of said condensates and polymers thereof and a curing catalyst for the aminoplast.
3. A composition of matter which comprises an aqueous solution of a water-soluble alkali metal lower alkyl siliconate, a water-soluble melamine-formaldehyde condensate and a curing catalyst for the melamine-formaldehyde condensate.
4. A composition according to claim 3 in which the melamine-formaldehyde condensate comprises methylated trirnethylol melamine.
5. A composition of matter which comprises an aqueous solution of parts by weight of sodium methyl siliconate, between about 25 and about 1000 parts of methylated trimethylol melamine and a sufficient quantity of a curing catalyst to cure the methylated trimethylol melamine to the water-insoluble state.
6. A process which comprises contacting a textile material with a composition according to claim 1 and heating the treated material to dry and cure said composition to the substantially water-insoluble'state, whereby a durable water-repellent finish is imparted to the textile material.
7. A process which comprises contacting a textile material with a composition according to claim 2 and heating the treated material to dry and cure said composition to the substantially water-insoluble state, whereby a durable water-repellent finish is imparted to the textile material.
8. A process which comprises contacting a textile material with a composition according to claim 3 and heating the treated material to dry and cure said composition to the substantially water-insoluble state, whereby a durable water-re ellent finish is imparted to the textile material.
9. A process which contacting a textile material with a composition according to claim 4 and heating the treated m terial to dry and cure said composition to the substantially water-insoluble state, whereby a durable water-repellent finish is imparted to the textile material.
10. A process which comprises contacting a textile material with a composition according to claim 5 in sufiicient quantity to deposit a total of at least 2 percent of said siliconate and melamine resin thereon based on the weight of the dry textile material and heating the treated material to a temperature of at least degrees Fahrenheit for a period sufiicient to dry and cure said composition to the substantially water-insoluble state, whereby a durable water-repellent finish is imparted to the textile material.
11. An article which comprises a textile material impregnated with the heat-cured reaction product of a composition according to claim 1.
12. An article which comprises a textile material impregnated with the heat-cured reaction product of a composition according to claim 2.
13. An article which comprises a textile material impregnated with the heat-cured reaction product of a composition according to claim 3.
14. An article which comprises a textile material impregnated with the heat-cured reaction product of a composition according to claim 4.
15. A textile article having a durable water-repellent finish which comprises a textile material impregnated with at least 2 percent by weight of the heat-cured reaction product of a composition according to claim 5.
" n HA" References titted in the file of this patent UNlTED STATES PATENTS 2,500,842 MacKenZie Mar. 14, 1950 2,507,200 Elliott May 9, 1950 2,571,029 Goodwin Oct. 9, 1951 2,612,482 Rasmussen Sept. 30, 1952 2,634,285 Rust Apr. 7, 1953
Claims (1)
1. A COMPOSITION OF MATTER WHICH COMPRISES AN AQUEOUS SOLUTION OF WATER-SOLUBLE METAL SALT OF A HYDROCARBON SILANETORIOL AND A WATER-SOLUBLE THERMOSETTING AMINOPLAST OF THE GROUP CONSISTING OF FORMALDEHYDE CONDENSATES OF MELAMINE, UREA, ETHYLENEUREA, SUCCINAMIDE, ADIPAMIDE, ALKYL ETHERS OF SAID CONDENSATES AND POLYMERS THEREOF.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US440848A US2785145A (en) | 1954-07-01 | 1954-07-01 | Siliconate-aminoplast compositions and textiles coated therewith |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US440848A US2785145A (en) | 1954-07-01 | 1954-07-01 | Siliconate-aminoplast compositions and textiles coated therewith |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2785145A true US2785145A (en) | 1957-03-12 |
Family
ID=23750423
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US440848A Expired - Lifetime US2785145A (en) | 1954-07-01 | 1954-07-01 | Siliconate-aminoplast compositions and textiles coated therewith |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2785145A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2819189A (en) * | 1954-11-15 | 1958-01-07 | American Cyanamid Co | Process of sizing textile yarn and product thereof |
| US2839430A (en) * | 1955-08-26 | 1958-06-17 | Du Pont | Antistatic agents for hydrophobic fiber |
| US2839431A (en) * | 1955-08-26 | 1958-06-17 | Du Pont | Antistatic agents for hydrophobic fiber |
| US2937155A (en) * | 1957-03-01 | 1960-05-17 | American Cyanamid Co | Composition containing alkyl silane triol and aminoplast resin and article coated therewith |
| US3043718A (en) * | 1959-07-09 | 1962-07-10 | Rohm & Haas | Compositions, textiles treated therewith, and processes for the treatment thereof |
| US3871909A (en) * | 1972-06-22 | 1975-03-18 | Warnaco Inc | Hosiery finishing process for treating fabrics containing spandex yarn |
| US4045385A (en) * | 1974-12-03 | 1977-08-30 | Dynamit Nobel Aktiengesellschaft | Free-flowing urea resin compositions with silane or siloxane additive added before hardening |
| US20090176094A1 (en) * | 2005-12-28 | 2009-07-09 | Kao Corporation | Fibre Modified By Application Of An Organosiliconate Agent, A Fibre Modifying Agent Comprising An Organosilikonate and A Method of Modifying A Fibre With Said Agent |
| DE102013209170A1 (en) | 2013-05-17 | 2013-09-12 | Cht R. Beitlich Gmbh | Composition useful e.g. for waterproofing of absorbent materials, comprises silicone polymer, wax and/or fatty acid esters, aminoplast, urea derivatives and/or melamine derivatives, solvent, crosslinking agent, and dispersing auxiliaries |
| WO2016146437A1 (en) | 2015-03-16 | 2016-09-22 | Cht R. Beitlich Gmbh | Fluorine-free hydrophobization |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2500842A (en) * | 1944-02-08 | 1950-03-14 | Montclair Res Corp | Aminotriazine-organosilicon composition |
| US2507200A (en) * | 1945-02-10 | 1950-05-09 | Gen Electric | Process for rendering materials water-repellent and compositions therefor |
| US2571029A (en) * | 1951-10-09 | Organosilicon resins | ||
| US2612482A (en) * | 1950-03-17 | 1952-09-30 | Gen Electric | Water-repellent compositions |
| US2634285A (en) * | 1947-03-27 | 1953-04-07 | Montclair Res Corp | Acyloxy silanes |
-
1954
- 1954-07-01 US US440848A patent/US2785145A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2571029A (en) * | 1951-10-09 | Organosilicon resins | ||
| US2500842A (en) * | 1944-02-08 | 1950-03-14 | Montclair Res Corp | Aminotriazine-organosilicon composition |
| US2507200A (en) * | 1945-02-10 | 1950-05-09 | Gen Electric | Process for rendering materials water-repellent and compositions therefor |
| US2634285A (en) * | 1947-03-27 | 1953-04-07 | Montclair Res Corp | Acyloxy silanes |
| US2612482A (en) * | 1950-03-17 | 1952-09-30 | Gen Electric | Water-repellent compositions |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2819189A (en) * | 1954-11-15 | 1958-01-07 | American Cyanamid Co | Process of sizing textile yarn and product thereof |
| US2839430A (en) * | 1955-08-26 | 1958-06-17 | Du Pont | Antistatic agents for hydrophobic fiber |
| US2839431A (en) * | 1955-08-26 | 1958-06-17 | Du Pont | Antistatic agents for hydrophobic fiber |
| US2937155A (en) * | 1957-03-01 | 1960-05-17 | American Cyanamid Co | Composition containing alkyl silane triol and aminoplast resin and article coated therewith |
| US3043718A (en) * | 1959-07-09 | 1962-07-10 | Rohm & Haas | Compositions, textiles treated therewith, and processes for the treatment thereof |
| US3871909A (en) * | 1972-06-22 | 1975-03-18 | Warnaco Inc | Hosiery finishing process for treating fabrics containing spandex yarn |
| US4045385A (en) * | 1974-12-03 | 1977-08-30 | Dynamit Nobel Aktiengesellschaft | Free-flowing urea resin compositions with silane or siloxane additive added before hardening |
| US20090176094A1 (en) * | 2005-12-28 | 2009-07-09 | Kao Corporation | Fibre Modified By Application Of An Organosiliconate Agent, A Fibre Modifying Agent Comprising An Organosilikonate and A Method of Modifying A Fibre With Said Agent |
| DE102013209170A1 (en) | 2013-05-17 | 2013-09-12 | Cht R. Beitlich Gmbh | Composition useful e.g. for waterproofing of absorbent materials, comprises silicone polymer, wax and/or fatty acid esters, aminoplast, urea derivatives and/or melamine derivatives, solvent, crosslinking agent, and dispersing auxiliaries |
| WO2016146437A1 (en) | 2015-03-16 | 2016-09-22 | Cht R. Beitlich Gmbh | Fluorine-free hydrophobization |
| DE102015204736A1 (en) | 2015-03-16 | 2016-09-22 | Cht R. Beitlich Gmbh | Fluorine-free hydrophobing |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3784356A (en) | Cellulosic flame retardant system | |
| GB2084205A (en) | Composition suitable for treating textile fabrics | |
| US2785145A (en) | Siliconate-aminoplast compositions and textiles coated therewith | |
| US2901463A (en) | Compositions, textiles treated therewith and processes for the treatment thereof | |
| US2795513A (en) | Process for finishing textile material and product | |
| US2828228A (en) | Textile fire retardant treatment | |
| US3079279A (en) | Blends of imidazolidinones and aminoplasts and method for finishing cellulose containing textile material | |
| US3380850A (en) | Treatment of synthetic polyamide textile material to improve its moisture absorbency and to reduce its electrification and soiling tendencies | |
| US3619113A (en) | Flame-retardant finish for cellulosic textile materials | |
| US3101278A (en) | Flame proofing of cellulosic materials | |
| US3288553A (en) | Process for treating napped fabrics | |
| US4295847A (en) | Finishing process for textiles | |
| US3627556A (en) | Durable press finish for wool/cellulosic fabrics (melamine/dihydroxy-imidazolidinone resins) | |
| US3335113A (en) | Process for preparing polymethylol ureas | |
| US3864076A (en) | Process for flameproofing organic fibers with phosphorus-containing condensation products and the products produced | |
| US3087905A (en) | Durable fluorochemical-melamine resin textile finish | |
| US3888779A (en) | Flame retardant composition containing tetrakis (hydroxymethyl) phosphonium oxalate | |
| US3032442A (en) | Process of finishing textiles with silicone-colloidal melamine resin mixtures, composition and resultant article | |
| US3168415A (en) | Textile finishing composition, application process, and resulting product | |
| US3067159A (en) | Aqueous water repellent dispersions comprising a methylene dialkylamide, a methylol cndensate, and a non-ionic surface active agent | |
| US3317345A (en) | Rot-resistant finish for textile materials | |
| US3378397A (en) | Highly alkylolated textile finishing composition and process for treating textile fabric therewith | |
| US2928758A (en) | Treating process | |
| US3085909A (en) | Silver containing reaction products, methods for their production and use in formingpermanent silver containing deposits on base materials | |
| US3533728A (en) | Inorganic and/or organic cellulose swelling agents used in conjunction with cross-linking agents in fabric modification process |