US2097589A - Treatment of textile materials - Google Patents
Treatment of textile materials Download PDFInfo
- Publication number
- US2097589A US2097589A US37781A US3778135A US2097589A US 2097589 A US2097589 A US 2097589A US 37781 A US37781 A US 37781A US 3778135 A US3778135 A US 3778135A US 2097589 A US2097589 A US 2097589A
- Authority
- US
- United States
- Prior art keywords
- film
- materials
- solution
- cellulose
- fabric
- 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
- 239000000463 material Substances 0.000 title description 85
- 239000004753 textile Substances 0.000 title description 52
- 238000011282 treatment Methods 0.000 title description 16
- 239000000126 substance Substances 0.000 description 46
- 239000000243 solution Substances 0.000 description 40
- 239000004744 fabric Substances 0.000 description 31
- 229920002678 cellulose Polymers 0.000 description 30
- 239000001913 cellulose Substances 0.000 description 27
- 229920002301 cellulose acetate Polymers 0.000 description 22
- 238000000034 method Methods 0.000 description 16
- 239000003795 chemical substances by application Substances 0.000 description 15
- 150000002736 metal compounds Chemical class 0.000 description 15
- 230000008569 process Effects 0.000 description 14
- 238000009991 scouring Methods 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 12
- 239000010408 film Substances 0.000 description 11
- 229920002955 Art silk Polymers 0.000 description 10
- 239000012991 xanthate Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 229910019142 PO4 Inorganic materials 0.000 description 7
- 239000003153 chemical reaction reagent Substances 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 235000021317 phosphate Nutrition 0.000 description 7
- -1 unsaturated aliphatic aldehydes Chemical class 0.000 description 7
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 6
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 238000009833 condensation Methods 0.000 description 5
- 230000005494 condensation Effects 0.000 description 5
- 239000007859 condensation product Substances 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000012736 aqueous medium Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 150000004706 metal oxides Chemical class 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 230000021736 acetylation Effects 0.000 description 2
- 238000006640 acetylation reaction Methods 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 229920001289 polyvinyl ether Polymers 0.000 description 2
- 229910052712 strontium Inorganic materials 0.000 description 2
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- FOHHNHSLJDZUGQ-UHFFFAOYSA-N 3-(dibutylamino)-1-[1,3-dichloro-6-(trifluoromethyl)-9-phenanthrenyl]-1-propanol Chemical compound FC(F)(F)C1=CC=C2C(C(O)CCN(CCCC)CCCC)=CC3=C(Cl)C=C(Cl)C=C3C2=C1 FOHHNHSLJDZUGQ-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 239000000899 Gutta-Percha Substances 0.000 description 1
- 240000002636 Manilkara bidentata Species 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 240000000342 Palaquium gutta Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 102100029469 WD repeat and HMG-box DNA-binding protein 1 Human genes 0.000 description 1
- 101710097421 WD repeat and HMG-box DNA-binding protein 1 Proteins 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 235000016302 balata Nutrition 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000012505 colouration Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- WCOATMADISNSBV-UHFFFAOYSA-K diacetyloxyalumanyl acetate Chemical compound [Al+3].CC([O-])=O.CC([O-])=O.CC([O-])=O WCOATMADISNSBV-UHFFFAOYSA-K 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- XJELOQYISYPGDX-UHFFFAOYSA-N ethenyl 2-chloroacetate Chemical compound ClCC(=O)OC=C XJELOQYISYPGDX-UHFFFAOYSA-N 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 229920000588 gutta-percha Polymers 0.000 description 1
- 229960003242 halofantrine Drugs 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- 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
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/327—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
- D06M15/333—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/07—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof
- D06M11/11—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof with halogen acids or salts thereof
- D06M11/20—Halides of elements of Groups 4 or 14 of the Periodic Table, e.g. zirconyl chloride
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/45—Oxides or hydroxides of elements of Groups 3 or 13 of the Periodic Table; Aluminates
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/68—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof
- D06M11/70—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with phosphorus or compounds thereof, e.g. with chlorophosphonic acid or salts thereof with oxides of phosphorus; with hypophosphorous, phosphorous or phosphoric acids or their salts
- D06M11/71—Salts of phosphoric acids
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/77—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
- D06M11/79—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof with silicon dioxide, silicic acids or their salts
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/80—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with boron or compounds thereof, e.g. borides
- D06M11/82—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with boron or compounds thereof, e.g. borides with boron oxides; with boric, meta- or perboric acids or their salts, e.g. with borax
-
- 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
- D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
- D06M15/03—Polysaccharides or derivatives thereof
- D06M15/05—Cellulose or derivatives thereof
- D06M15/07—Cellulose esters
-
- 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
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/02—Natural fibres, other than mineral fibres
- D06M2101/04—Vegetal fibres
- D06M2101/06—Vegetal fibres cellulosic
-
- 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
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/02—Natural fibres, other than mineral fibres
- D06M2101/04—Vegetal fibres
- D06M2101/06—Vegetal fibres cellulosic
- D06M2101/08—Esters or ethers of cellulose
-
- 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
Definitions
- This invention relates to improvements in the treatment of textile materials, and is more particularly concerned with fixing therein insoluble substances and particularly insoluble metal oxides or compounds.
- the invention is particularly valuable in the treatment of artificial textile materials, for example those of cellulosic character or those made of cellulose acetate or other organic derivatives of cellulose.
- Such processes involve the successive application of two or more soluble reagents to the materials with resultant precipitation in or on the materials of insoluble metal oxides or compounds While these processes have the advantage that stocks of artificial silk of normal bright lustre can readily be converted into materials of dull lustre,- nevertheless the fastness of the delustring agent upon the material frequently leaves something to be desired. In particular in scouring and in other normal finishing processes, and in domestic washing or other laundering operations, the delustring agent or some of it is liable to be removed with consequent change in the appearance of the artificial silk.
- artificial silk made of cellulose derivatives may be loaded with tin 45 compounds, for example by treatment with a stannic chloride solution followed by fixation with phosphate and/or silicate solution. It is desirable in order to obtain any'substantial loading of the material to apply the tin salt or other solution containing the loading metal radicle under conditions such that the cellulose derivative is in a swollen condition.
- the material may be treated with a swelling agent.
- stannic chloride or similar loading bath may be included in the stannic chloride or similar loading bath, or alternatively the stannlc chloride or similar loading agent may be applied under such conditions of concentration and temperature-that it constitutes a swelling agent for the material under treatment.
- stannic chloride, phosphate and/or 5 silicate other insoluble loading agentsmay be formed in or on the materials, for example phosphates, silicates, borates and the like of the alkaline earth metals, for instance calcium, barium, strontium or of lead or other heavy metals.
- the silicate, phosphate or like fixing agent though preferably applied subsequent to the stannicchloride or other metal loading solution, may be applied prior thereto. Where materials containing saponifiable organic esters of cellulose are being treated, the silicate, phosphate or other fixing agent, whether 20 applied prior to or subsequent to the metallic loading solution, may effect a saponification of the cellulose ester. In such loading processes,
- insoluble coloured pigments may be formed in or on the material for the purpose of imparting colourations which are faster to light than are theusual dyeings produced 30 with organic dyestufis. Any lack of fastness to scouring, washing or similar treatments obviously counterbalances the increased fastness to lightof the colouring agent.
- the object of the present invention to 35. improve the fastness to scouring, washing and similar treatments of insoluble substances fixed in or on textile materials.
- the fastness of such insoluble substances in or on the textile materials is improved by applying to the textiles a film-forming substance insoluble or substantially insoluble in water or the. usual scouring-liquids.
- a film-forming substance insoluble or substantially insoluble in water or the. usual scouring-liquids.
- such film forming substance is applied in very small amounts so that the properties of the materials as textiles are in no way impaired.
- the film-. forming materials may be applied to the textiles in very low proportions, and particularly in amounts 'of under 5% by weight of the textile under treatment. Proportions as low as 3, 2, and- 1% or under may be'used with advantage and still improve the fastness of the insoluble compounds fixed in or on the textile materials.
- a further important feature of the present invention consists in applying the film-forming substances from dilute solutions or dispersions so thatlittie or no sticking of the individual filaments, fibres or yarns of the'textiles takes place For instance with this object in view it is desirable to apply the film-forming substances in solutions or dispersions of a concentration under 5% and preferably as low as 2 or 1% or less.
- the present invention embraces quite broadly the application of any film-forming substance which is insoluble or substantially insoluble in water and in the ordinary scouring and washing baths.
- a wide variety of film-forming substances is available for the purpose, for example polymerized unsaturated organic compounds generally, for instance polymerized vinyl acetate, polymerized vinyl chloracetate and other polymerized vinyl esters, polyvinyl ethers,polystyreneandsimilar polymerized unsaturated hydrocarbons, polymerized unsaturated aliphatic aldehydes, polymerized esters of unsaturated aliphatic acids, for instance, polymerized acrylic ester and polymerized methacrylie ester; various film-forming condensation products, including urea formaldehyde condensation products, phenol aldehyde condensation products and mixed phenol urea aldehyde condensation products, condensation productsof polyalcohols with polybasic acids, e.
- alkyd resins made, for example, by the condensation of glycerin with phthalic anhydrlde, and modified alkyd resins, made by reaction between an alkyd resin and an oil or a higher fatty acid.
- alkyd resins made, for example, by the condensation of glycerin with phthalic anhydrlde, and modified alkyd resins, made by reaction between an alkyd resin and an oil or a higher fatty acid.
- Such polymerization and/or condensation products may be applied in the fully polymerized and/or condensed form, provided they are soluble or dispersible in organic liquids or in aqueous liquids, or they may be applied in apartially polymerized and/or condensed form, with or without subsequent further polymerization or condensation upon the material.
- the reagents in the unpolymerized or uncondensed form may be applied to the materials and the .whole of the polymerization and/or condensation desired effected upon the materials. Generally it is undesirable to employ in such polymerization and/or condensation processes carried out on the materials, temperatures in excess of about 180 C. Preferably temperatures below 150 C. are employed.
- the ordinary alkali metal cellulose xanthate solution may be employed or any other soluble or dispersible cellulose xanthate, for example, ammonium cellulose xanthate or a cellulose xanthate of an organic amino base or magnesium cellulose xanthate.
- Chlorinated rubber is also suitable as a, film-forming substance for the purpose of the present invention.
- Rubber itself is suitable for increasing the fastness of the loading, delustring or other compounds but has the disadvantage that it tends to oxidize in theair. especially in the very thin films in which it is applied according' to the present invention. Balata, gutta percha and like bodies have similar properties.
- the invention particularly contemplates the application of very small proportions of film-forming substances to the textile materials, and to achieve this low concentrations of the film-forming substances in suitable solvent or dispersion media are especially valuable.
- the invention more particularly contemplates the application of the film-forming substance to the textile material already loaded with the loading, delustring or other agent.
- the film-forming substance may, where feasible, be included in" one or other of the reagents for forming the loading, delustring or other compound upon the material.
- Latex for example, may be included in a neutral or alkaline reagent; Similar remarks apply to the alkali metal cellulose xanthates, ammonium and amine cellulose xanthates and magnesium cellulose xanthate.
- an insoluble borate, silicate or phosphate is being formed upon the material
- a xanthate or other film-forming substance stable, in the presence of alkali or neutral media
- a neutral or alkaline aqueous solution of an alkali metal, silicate, phosphate or borate used for fixing upon the material the loading or delustring metal, for example tin, barium, strontium, calcium and magnesium.
- a film-forming substance may be included in such a fixing solution, whether the fixing agent be ap plied before or after the metal salt solution. Further, where feasible a film-forming substance -may be dissolved or dispersed in the solution of the insoluble substance upon the materials, the
- the medium in which it is applied will generally be an aqueous medium. Where it is applied subsequent to the formation. on the material of the loading, delustring or other agent, it may be ap plied either in an aqueous or in an organic me-' dium.
- the film-forming substances are insoluble in water, so that for application in aqueous media they must be dispersed. However, the film-forming substances may be present in aqueous solution in a soluble form and may beconverted upon the material into an insoluble form.
- viscose and cuprammonium-cellulose and various unpolymerised or uncondensed reagents or partially polymerized and/or condensed substances to be subsequently polymerized or condensed or further polymerized or condensed on the textile material.
- a viscose solution may be applied to a loaded cellulose acetate fabric and may be subsequently steamed or treated with a solution of ammonium acetate, acetic acid, sulphuric acid or other precipitant for the xanthate.
- ethers, or ether-esters the polyvinyl esters, ethers or other compounds, the polymerized acrylic esters and similar polymerized unsaturated esters, and the polymerized aldehydes are most conveniently applied from an organic solvent, for example methyl .or ethyl alcohol or other alcohol; acetone, methyl ethyl ketone or other ketone;
- glycols glycerine glycol ethers, glycol esters and glycol ether-esters, methyl formate, ethyl formate;
- the medium in which the film-forming substance is applied to the textile material cellulose derivatives.
- the film-forming substance may be of the same chemical character as the textile material under treatment.
- a cellulose derivative fabric may be coated with a thin film of cellulose derivative.
- the film-forming cellulose derivative shall have diflerent solubility properties from those of the cellulose derivative present in the textile material.
- the film-forming substance may be identical or substantially identical with the substance of the textile.
- a loaded or delustred cellulose acetate fabric may have a cellulose acetate applied thereto.
- a cellulose acetate can readily be prepared which is soluble to the required extent in such an aqueoussumble, even at ordinary temperatures, by arranging the conditions of acetylation, including pre-treatmerit, acetylation proper and ripening, so as to yield a cellulose acetate of comparatively low viscosity.
- a suitable cellulose acetate may, for example, be dissolved to a concentration of about 1% in a 20-35% aqueous solution of acetic acid at IO- C. and applied in this form to a cellulose acetate fabric. Preferably after the application of the solution the fabric is rapidly cooled. Evaporation of the solvent may be eifected at low or relatively low temperatures.
- the solvent may be so chosen that it is a solvent for the film-forming substance while hot and a non-solvent when cold, so that a hot solution may be applied to the textile and the film-forming substance precipitated thereon by mere cooling.
- the film-forming substance may be applied to A the textile materials by any suitable method, for example mechanical impregnation, bath treatments, spraying or the like. impregnation followed by a squeezing of the fabric so that it re-' tains a predetermined amount ofthe film-forming solution or dispersion is particularly useful for the purpose of the present invention, since it enables a very uniform application of the filmforming substance in the desired small quantity to be achieved very readily.
- a loaded or delustredtextile fabric may, for example. be passed through a solution or dispersion of the film-forming substance in a bath or in a padding mangle and the fabric squeezed so as to retain 50,. or
- a very convenient procedure consists in applying tothe fabric a solution of ,the film-forming substance in a concentration of 1A to 1 or 2% and subsequently expressing the film-forming solution so that the fabric contains a quantity of.50-100% of its own weight of the solution.
- Example 1 A fabric of natural silk yarn is steeped in a stannic chloride solution of 40-50 Tw. for half an hour at a temperature of 40-50 C., thoroughly rinsed and then steeped in a solution of disodium phosphate of 4-6" Tw. for halfan hour at 40-45 C. The fabric is rinsed, washed in soap solution, rinsed again and then dried.
- the dry, loaded fabric is then treated with a 1% solution of cellulose acetate in acetone, passed through nipping rollers to express the solution so that the fabric retains about its own weight of the solution, and dried.
- the film of' cellulose acetate thus formed on the loaded fabric appreciably reduces the loss in weight occasioned by repeated scouring without changing the appearance of the fabric.
- Example 2 A fabric of cellulose acetate yarn is steeped for 1 hourat about 20? C. in a loading bath containing about 280 grams of stannic chloride (SnChfiHsO) and 243 grams of ammonium thiocyanate per litre. The fabric is removed from the bath, drained well and washed first in two baths of cold water and then in two baths cf water at 45 C. until quite free from soluble salts.
- stannic chloride SnChfiHsO
- the film of polymerized vinyl acetate thus formed on the fabric appreciably reduces the loss in weight occasioned by repeated scouring without altering the appearance or dyeing properties of the fabric.
- Example 3 A fabric of cellulose acetate yarn is treated with a fairly concentrated solution of sodium aluminate, centrifuged and then, while still moist, stretched out or hung in a chamber in which it is exposed at 50-70 C. to the moist carbon dioxide. The fabric is then washed until free from sodium carbonate and dried.
- the fabric loaded with aluminium hydroxide thus obtained is treated with a solution of viacose containing 2% of cellulose for half a minute at 26 C. and squeezed so that it retains about its own weight of solution.
- the fabric is then placed in a precipitating bath, consisting of a aqueous solution of aluminium acetate. for 2 minutes at 26 C.
- the fabric is then thoroughly washed and dried.
- the step which comprises improving the fastness of said metal compound without substantially impairing the properties of the textile'materials by applying to the textile materials impregnated therewith a solution in a volatile desire to secure by Letters organic solvent of a substance which forms a film on the materials which is substantially'insoluble in aqueous scouring liquids, the film forming-substance being applied in a quantity less than 5% of the weight of the textile materials treated.
- the step which comprises improving the fastness of said metal compound without substantially impairing the properties of the textile materials by applying to the textile materials p nated therewith a solution in a volatile organic solvent of a substance which forms a film on the materials which is substantially insoluble in aqueous scouring liquids, the filmforming substance being applied in a quantity equal to $5 to 2% of the weightof the textile 'materials treated.
- the step which comprises improving the fastness of said metal compound without sub stantially impairing the properties of the textile materials by applying to the textile materials impregnated therewith a solution of cellulose acetate in a volatile organic solvent so as to form a film of cellulose acetate on the materials which is substantially insoluble in aqueous scouring liquids, the film-forming substance being applied in quantity less than 5% of the weight of the textile materials treated.
- the step which comprises improving the fastness of said metal compound without substantially impairing the properties of the textile materials by applying to the textile materials impregnated therewith a $6 to 2% solution of cellulose acetate in a volatile organic solvent so as to form a film of cellulose acetate on the materials which is substantially insoluble in aqueous scouring liquids, the quantity of cellulose acetate applied being equal to A to'2% of the weight of the textile materials treated.
- step 8 which comprises improving the fastness of said metal compound without substantially impairing the properties of the textile materials by applying to the textile materials impregnated therewith a it to 2% solution in a volatile organic solvent of vinyl acetate so as to form a film of vinyl acetate on the materials which is substantially insoluble in aqueous scouring liquids, the vinyl acetate being applied in a quantity equal to V to 2% of the weight of the materials treated.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
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Description
Patented Nov. 2, 1937 PATENT v OFFICE I TREATMENT OF TEXTILE MATERIALS Henry Dreyfus, London, England No Drawing. Application August 24, 1935, Serial No. 37,781. In Great Britain August so, 1934 s Claims. (01. 91-68) This invention relates to improvements in the treatment of textile materials, and is more particularly concerned with fixing therein insoluble substances and particularly insoluble metal oxides or compounds. The invention is particularly valuable in the treatment of artificial textile materials, for example those of cellulosic character or those made of cellulose acetate or other organic derivatives of cellulose.
10 Recently considerable research has been carried out with a view to decreasing or modifying the normal high lustre of artificial silk materials by incorporating therein white opaque compounds, generally insoluble metal oxides or other metal compounds. Proposals to this end have included spinning the artificial silk from solutions containing in suspension the finely divided metal oxides or compounds. Such processes, while yielding artificial silk of dull lustre, necessitate providing stocks of artificial silk both of dull lustre and ordinary bright lustre. Other processes effect a dulling of the lustre of artificial silk after its formation. Such processes involve the successive application of two or more soluble reagents to the materials with resultant precipitation in or on the materials of insoluble metal oxides or compounds While these processes have the advantage that stocks of artificial silk of normal bright lustre can readily be converted into materials of dull lustre,- nevertheless the fastness of the delustring agent upon the material frequently leaves something to be desired. In particular in scouring and in other normal finishing processes, and in domestic washing or other laundering operations, the delustring agent or some of it is liable to be removed with consequent change in the appearance of the artificial silk.
Similarly, for certain purposes it is desirable to load artificial silk not with the object of dulling its lustre but with the object of imparting to it a fuller handle and/or with the object of increasing its safe ironing point or of modifying the dyeing properties. Thus, for instance, artificial silk made of cellulose derivatives may be loaded with tin 45 compounds, for example by treatment with a stannic chloride solution followed by fixation with phosphate and/or silicate solution. It is desirable in order to obtain any'substantial loading of the material to apply the tin salt or other solution containing the loading metal radicle under conditions such that the cellulose derivative is in a swollen condition. For example the material may be treated with a swelling agent. or a swelling agent may be included in the stannic chloride or similar loading bath, or alternatively the stannlc chloride or similar loading agent may be applied under such conditions of concentration and temperature-that it constitutes a swelling agent for the material under treatment.- Instead of loading with stannic chloride, phosphate and/or 5 silicate, other insoluble loading agentsmay be formed in or on the materials, for example phosphates, silicates, borates and the like of the alkaline earth metals, for instance calcium, barium, strontium or of lead or other heavy metals. Some 30 of these metal compounds, particularly the alkaline earth compounds, have the effect of dlminishing the lustre of the materlal in addition to imparting a substantial loading. The silicate, phosphate or like fixing agent, though preferably applied subsequent to the stannicchloride or other metal loading solution, may be applied prior thereto. Where materials containing saponifiable organic esters of cellulose are being treated, the silicate, phosphate or other fixing agent, whether 20 applied prior to or subsequent to the metallic loading solution, may effect a saponification of the cellulose ester. In such loading processes,
' again the fastness in the material of the loading compound may sometimes with advantage be 2i improved. p
In a similar manner insoluble coloured pigments may be formed in or on the material for the purpose of imparting colourations which are faster to light than are theusual dyeings produced 30 with organic dyestufis. Any lack of fastness to scouring, washing or similar treatments obviously counterbalances the increased fastness to lightof the colouring agent. v
It is the object of the present invention to 35. improve the fastness to scouring, washing and similar treatments of insoluble substances fixed in or on textile materials. According to the present invention the fastness of such insoluble substances in or on the textile materials is improved by applying to the textiles a film-forming substance insoluble or substantially insoluble in water or the. usual scouring-liquids. Preferably such film forming substance is applied in very small amounts so that the properties of the materials as textiles are in no way impaired. Thus, the film-. forming materials may be applied to the textiles in very low proportions, and particularly in amounts 'of under 5% by weight of the textile under treatment. Proportions as low as 3, 2, and- 1% or under may be'used with advantage and still improve the fastness of the insoluble compounds fixed in or on the textile materials.
A further important feature of the present invention consists in applying the film-forming substances from dilute solutions or dispersions so thatlittie or no sticking of the individual filaments, fibres or yarns of the'textiles takes place For instance with this object in view it is desirable to apply the film-forming substances in solutions or dispersions of a concentration under 5% and preferably as low as 2 or 1% or less.
The difficulty as to the fastness to scouring and similar agencies of insolubleloading, delustring and similar agents arises more particularly with artificial textile materials. Cellulose derivative materials are sepecially improved by the process of the present invention. As is well known, these materials are relatively impervious to aqueous media and therefore difllculties arise in the loading, delustring and similar treatments of these materials wherein the reagents designed to form in the materials the delustring, loading and similar agents are applied in aqueous media. Usually it is necessary to swell the cellulose derivative duringthe treatment, and especially during the treatment with a soluble metallic comfpound. In sufi'icient penetration of the materials by the aqueous reagents may well be responsible for lack of fastness of the insoluble compound formed on the materials. Probably the smooth character of artificial silk materials also tends to render the loading, delustring or similar agent less fast to scouring-washing and like treatments.
- The present invention embraces quite broadly the application of any film-forming substance which is insoluble or substantially insoluble in water and in the ordinary scouring and washing baths. A wide variety of film-forming substances is available for the purpose, for example polymerized unsaturated organic compounds generally, for instance polymerized vinyl acetate, polymerized vinyl chloracetate and other polymerized vinyl esters, polyvinyl ethers,polystyreneandsimilar polymerized unsaturated hydrocarbons, polymerized unsaturated aliphatic aldehydes, polymerized esters of unsaturated aliphatic acids, for instance, polymerized acrylic ester and polymerized methacrylie ester; various film-forming condensation products, including urea formaldehyde condensation products, phenol aldehyde condensation products and mixed phenol urea aldehyde condensation products, condensation productsof polyalcohols with polybasic acids, e. g. the socalled alkyd resins, made, for example, by the condensation of glycerin with phthalic anhydrlde, and modified alkyd resins, made by reaction between an alkyd resin and an oil or a higher fatty acid. Such polymerization and/or condensation products may be applied in the fully polymerized and/or condensed form, provided they are soluble or dispersible in organic liquids or in aqueous liquids, or they may be applied in apartially polymerized and/or condensed form, with or without subsequent further polymerization or condensation upon the material. If desired the reagents in the unpolymerized or uncondensed form may be applied to the materials and the .whole of the polymerization and/or condensation desired effected upon the materials. Generally it is undesirable to employ in such polymerization and/or condensation processes carried out on the materials, temperatures in excess of about 180 C. Preferably temperatures below 150 C. are employed.
Other film-forming bodies which are useful for the purpose of the present invention include cellulose and cellulose derivatives, for example nitrocellulose, cellulose acetate, formate, propionate,
'butyrate and benzoate, methyl-, ethylor benzylcelluloses' or other cellulose esters or cellulose ethers or mixed esters, mixed ethers or mixed ether-esters, for instance oxyethyl cellulose acetate; and solutions of cellulose including viscose and cuprammonium cellulose. The ordinary alkali metal cellulose xanthate solution may be employed or any other soluble or dispersible cellulose xanthate, for example, ammonium cellulose xanthate or a cellulose xanthate of an organic amino base or magnesium cellulose xanthate. Chlorinated rubber is also suitable as a, film-forming substance for the purpose of the present invention. Rubber itself is suitable for increasing the fastness of the loading, delustring or other compounds but has the disadvantage that it tends to oxidize in theair. especially in the very thin films in which it is applied according' to the present invention. Balata, gutta percha and like bodies have similar properties.
As previously indicated, the invention particularly contemplates the application of very small proportions of film-forming substances to the textile materials, and to achieve this low concentrations of the film-forming substances in suitable solvent or dispersion media are especially valuable. The invention more particularly contemplates the application of the film-forming substance to the textile material already loaded with the loading, delustring or other agent.
If desired, however, the film-forming substance may, where feasible, be included in" one or other of the reagents for forming the loading, delustring or other compound upon the material. Latex, for example, may be included in a neutral or alkaline reagent; Similar remarks apply to the alkali metal cellulose xanthates, ammonium and amine cellulose xanthates and magnesium cellulose xanthate. Thus, for instance, where an insoluble borate, silicate or phosphate is being formed upon the material, such a xanthate or other film-forming substance, stable, in the presence of alkali or neutral media, may be dissolved or dispersed in a neutral or alkaline aqueous solution of an alkali metal, silicate, phosphate or borate used for fixing upon the material the loading or delustring metal, for example tin, barium, strontium, calcium and magnesium. The
' film-forming substance may be included in such a fixing solution, whether the fixing agent be ap plied before or after the metal salt solution. Further, where feasible a film-forming substance -may be dissolved or dispersed in the solution of the insoluble substance upon the materials, the
medium in which it is applied will generally be an aqueous medium. Where it is applied subsequent to the formation. on the material of the loading, delustring or other agent, it may be ap plied either in an aqueous or in an organic me-' dium. Generally the film-forming substances are insoluble in water, so that for application in aqueous media they must be dispersed. However, the film-forming substances may be present in aqueous solution in a soluble form and may beconverted upon the material into an insoluble form. Such is the case with viscose and cuprammonium-cellulose and various unpolymerised or uncondensed reagents or partially polymerized and/or condensed substances to be subsequently polymerized or condensed or further polymerized or condensed on the textile material. For instance, a viscose solution may be applied to a loaded cellulose acetate fabric and may be subsequently steamed or treated with a solution of ammonium acetate, acetic acid, sulphuric acid or other precipitant for the xanthate.
Cellulose acetate and similar cellulose esters,
ethers, or ether-esters, the polyvinyl esters, ethers or other compounds, the polymerized acrylic esters and similar polymerized unsaturated esters, and the polymerized aldehydes are most conveniently applied from an organic solvent, for example methyl .or ethyl alcohol or other alcohol; acetone, methyl ethyl ketone or other ketone;
glycols, glycerine glycol ethers, glycol esters and glycol ether-esters, methyl formate, ethyl formate;
for preventing damage to textiles consisting of I cellulose derivatives during theapplication of the film-forming substance.
Generally the medium in which the film-forming substance is applied to the textile material cellulose derivatives.
' should have no substantial solvent action upon the textile material. This isparticularly important with textile materials made of or containi However, some solvent actionof the medium in which the film-forming substance is applied upon the textile material under treatment is advantageous in that it appears to secure a better anchoring of the film-forming substance to the textile material. If desired the film-forming substance may be of the same chemical character as the textile material under treatment. For example a cellulose derivative fabric may be coated with a thin film of cellulose derivative.
It is desirable that the film-forming cellulose derivative shall have diflerent solubility properties from those of the cellulose derivative present in the textile material. If suitable precautions are taken, however, the film-forming substance may be identical or substantially identical with the substance of the textile. For instance a loaded or delustred cellulose acetate fabric may have a cellulose acetate applied thereto. The filmforming cellulose acetate may be such as will dissolve in a 30-40% aqueous solution of .acetone, acetic acid or dioxane at ordinary or high temperatures; Having regard to the low concentra= tions in which the film-forming substances are preferably applied according to the present invention, this presents no dimculty. A cellulose acetate can readily be prepared which is soluble to the required extent in such an aqueoussoivent, even at ordinary temperatures, by arranging the conditions of acetylation, including pre-treatmerit, acetylation proper and ripening, so as to yield a cellulose acetate of comparatively low viscosity. A suitable cellulose acetate may, for example, be dissolved to a concentration of about 1% in a 20-35% aqueous solution of acetic acid at IO- C. and applied in this form to a cellulose acetate fabric. Preferably after the application of the solution the fabric is rapidly cooled. Evaporation of the solvent may be eifected at low or relatively low temperatures. Instead of evaporating the solvent, the latter may be so chosen that it is a solvent for the film-forming substance while hot and a non-solvent when cold, so that a hot solution may be applied to the textile and the film-forming substance precipitated thereon by mere cooling.-
The film-forming substance may be applied to A the textile materials by any suitable method, for example mechanical impregnation, bath treatments, spraying or the like. impregnation followed by a squeezing of the fabric so that it re-' tains a predetermined amount ofthe film-forming solution or dispersion is particularly useful for the purpose of the present invention, since it enables a very uniform application of the filmforming substance in the desired small quantity to be achieved very readily. A loaded or delustredtextile fabric may, for example. be passed through a solution or dispersion of the film-forming substance in a bath or in a padding mangle and the fabric squeezed so as to retain 50,. or
% of its own weight of the solution or dispersion, and the fabric may thereafter be dried or otherwise treated to fix the'film-forming substance thereon. A very convenient procedure consists in applying tothe fabric a solution of ,the film-forming substance in a concentration of 1A to 1 or 2% and subsequently expressing the film-forming solution so that the fabric contains a quantity of.50-100% of its own weight of the solution.
As previously indicated, the process of the invention is of the greatest importance in relation toimproving the fastness of loading. delustring or other insoluble substance upon materials made r of or containing cellulose acetate or other cellulose derivatives. In this connection reference is made to the delustring or loading processes of U. S. applications S. Nos. 30,944 and 30,945 filed July 11, 1935 and applications S. Nos, 37,779 and. 37,780 filed Aug. 24, 1935. i
The following examples are given in order to illustrate the invention, but it is to be understood that they do not limit it in any way:-
Example 1 A fabric of natural silk yarn is steeped in a stannic chloride solution of 40-50 Tw. for half an hour at a temperature of 40-50 C., thoroughly rinsed and then steeped in a solution of disodium phosphate of 4-6" Tw. for halfan hour at 40-45 C. The fabric is rinsed, washed in soap solution, rinsed again and then dried.
The dry, loaded fabric is then treated with a 1% solution of cellulose acetate in acetone, passed through nipping rollers to express the solution so that the fabric retains about its own weight of the solution, and dried.
The film of' cellulose acetate thus formed on the loaded fabric appreciably reduces the loss in weight occasioned by repeated scouring without changing the appearance of the fabric.
Example 2 A fabric of cellulose acetate yarn is steeped for 1 hourat about 20? C. in a loading bath containing about 280 grams of stannic chloride (SnChfiHsO) and 243 grams of ammonium thiocyanate per litre. The fabric is removed from the bath, drained well and washed first in two baths of cold water and then in two baths cf water at 45 C. until quite free from soluble salts.
to the dry fabric in the form of a 135% solution in this solvent, the fabric being passed through nipping rollers to express the solution so that the fabric retains about its own weight of the solution, after which the fabric is dried.
The film of polymerized vinyl acetate thus formed on the fabric appreciably reduces the loss in weight occasioned by repeated scouring without altering the appearance or dyeing properties of the fabric.
Example 3 A fabric of cellulose acetate yarn is treated with a fairly concentrated solution of sodium aluminate, centrifuged and then, while still moist, stretched out or hung in a chamber in which it is exposed at 50-70 C. to the moist carbon dioxide. The fabric is then washed until free from sodium carbonate and dried.
The fabric loaded with aluminium hydroxide thus obtained is treated with a solution of viacose containing 2% of cellulose for half a minute at 26 C. and squeezed so that it retains about its own weight of solution. The fabric is then placed in a precipitating bath, consisting of a aqueous solution of aluminium acetate. for 2 minutes at 26 C. The fabric is then thoroughly washed and dried.
The fabric thus obtained does not suffer substantial loss in weight even after repeated scour- 8.
What I claim and Patent is:-
1. In a process for the manufacture of textile materials impregnated with an insoluble metal compound, the step which comprises improving the fastness of said metal compound without substantially impairing the properties of the textile'materials by applying to the textile materials impregnated therewith a solution in a volatile desire to secure by Letters organic solvent of a substance which forms a film on the materials which is substantially'insoluble in aqueous scouring liquids, the film forming-substance being applied in a quantity less than 5% of the weight of the textile materials treated.
2. In a proces for the manufacture of textile materials impregnated with an insoluble metalcompound, the step which comprises improving the fastness of said metal compound without substantially impairing the properties of the textile materials by applying to the textile materials p nated therewith a solution in a volatile organic solvent of a substance which forms a film on the materials which is substantially insoluble in aqueous scouring liquids, the filmforming substance being applied in a quantity equal to $5 to 2% of the weightof the textile 'materials treated.
the fastness of said metal compound without.
substantially impairing the properties of the textile materials by applying to the textile materials impregnated therewith a solution of less than 5% concentration in a volatile organic solvent of a substance which forms a film on the materials which is substantially insoluble in aqueous scourimpregnated therewith a solution of it to 2% concentration in a volatile organic solventof a substance which forms a film on the materials which is substantially insoluble in aqueous scouring liquids, the fllm-fomring substance being applied in a quantity equal to to 2% of the weight of the textile materials treated.
5. In a process for the manufacture of textile materials impregnated with an insoluble metal compound, the step which comprises improving the fastness of said metal compound without sub stantially impairing the properties of the textile materials by applying to the textile materials impregnated therewith a solution of cellulose acetate in a volatile organic solvent so as to form a film of cellulose acetate on the materials which is substantially insoluble in aqueous scouring liquids, the film-forming substance being applied in quantity less than 5% of the weight of the textile materials treated.
6. In a process for the manufacture of textile materials impregnated with an insoluble metal compound, the step which comprises improving the fastness of said metal compound without substantially impairing the properties of the textile materials by applying to the textile materials impregnated therewith a $6 to 2% solution of cellulose acetate in a volatile organic solvent so as to form a film of cellulose acetate on the materials which is substantially insoluble in aqueous scouring liquids, the quantity of cellulose acetate applied being equal to A to'2% of the weight of the textile materials treated.
I 7. In a process for the manufacture of textile -materials impregnated with an insoluble metal compound, the step which comprises improving the fastness of said metal compound without substantially impairing the properties of the textile materials by applying to the textile materials weight of the materials treated.
8. In a process for the manufacture of textile materials impregnated with an insoluble metal compound, the step which comprises improving the fastness of said metal compound without substantially impairing the properties of the textile materials by applying to the textile materials impregnated therewith a it to 2% solution in a volatile organic solvent of vinyl acetate so as to form a film of vinyl acetate on the materials which is substantially insoluble in aqueous scouring liquids, the vinyl acetate being applied in a quantity equal to V to 2% of the weight of the materials treated.
,- HENRY DREYFUSV
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB24986/34A GB445182A (en) | 1934-08-30 | 1934-08-30 | Improvements in the treatment of textile materials |
Publications (1)
Publication Number | Publication Date |
---|---|
US2097589A true US2097589A (en) | 1937-11-02 |
Family
ID=10220360
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US37781A Expired - Lifetime US2097589A (en) | 1934-08-30 | 1935-08-24 | Treatment of textile materials |
Country Status (2)
Country | Link |
---|---|
US (1) | US2097589A (en) |
GB (1) | GB445182A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2423428A (en) * | 1943-12-30 | 1947-07-01 | American Cyanamid Co | Pretreatment of cellulosic textiles with melamine formaldehyde resin |
EP0522304A1 (en) * | 1991-06-12 | 1993-01-13 | New Japan Chemical Co.,Ltd. | Natural cellulosic fibers treated with inorganic metal compounds and polycarboxylic acids |
US5427844A (en) * | 1991-06-12 | 1995-06-27 | New Japan Chemical Co., Ltd. | Articles of natural cellulose fibers with improved deodorant properties and process for producing same |
WO2002010499A2 (en) * | 2000-08-01 | 2002-02-07 | Unilever Plc | Textile treatment process and product |
US6562743B1 (en) | 1998-12-24 | 2003-05-13 | Bki Holding Corporation | Absorbent structures of chemically treated cellulose fibers |
US8946100B2 (en) | 2003-12-19 | 2015-02-03 | Buckeye Technologies Inc. | Fibers of variable wettability and materials containing the fibers |
CN116445231A (en) * | 2023-03-17 | 2023-07-18 | 苏州安侯医疗科技有限公司 | Anti-fog cleaning wet tissue and preparation method thereof |
-
1934
- 1934-08-30 GB GB24986/34A patent/GB445182A/en not_active Expired
-
1935
- 1935-08-24 US US37781A patent/US2097589A/en not_active Expired - Lifetime
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2423428A (en) * | 1943-12-30 | 1947-07-01 | American Cyanamid Co | Pretreatment of cellulosic textiles with melamine formaldehyde resin |
EP0522304A1 (en) * | 1991-06-12 | 1993-01-13 | New Japan Chemical Co.,Ltd. | Natural cellulosic fibers treated with inorganic metal compounds and polycarboxylic acids |
US5427844A (en) * | 1991-06-12 | 1995-06-27 | New Japan Chemical Co., Ltd. | Articles of natural cellulose fibers with improved deodorant properties and process for producing same |
US20030157857A1 (en) * | 1998-12-24 | 2003-08-21 | Bki Holding Corporation | Absorbent structures of chemically treated cellulose fibers |
US20040224588A1 (en) * | 1998-12-24 | 2004-11-11 | Bki Holding Corporation | Absorbent structures of chemically treated cellulose fibers |
US6562743B1 (en) | 1998-12-24 | 2003-05-13 | Bki Holding Corporation | Absorbent structures of chemically treated cellulose fibers |
US6770576B2 (en) | 1998-12-24 | 2004-08-03 | Bki Holding Corporation | Absorbent structures of chemically treated cellulose fibers |
WO2002010499A2 (en) * | 2000-08-01 | 2002-02-07 | Unilever Plc | Textile treatment process and product |
US6565924B2 (en) | 2000-08-01 | 2003-05-20 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Textile treatment process and product |
WO2002010499A3 (en) * | 2000-08-01 | 2002-04-18 | Unilever Plc | Textile treatment process and product |
US8946100B2 (en) | 2003-12-19 | 2015-02-03 | Buckeye Technologies Inc. | Fibers of variable wettability and materials containing the fibers |
US10300457B2 (en) | 2003-12-19 | 2019-05-28 | Georgia-Pacific Nonwovens LLC | Fibers of variable wettability and materials containing the fibers |
CN116445231A (en) * | 2023-03-17 | 2023-07-18 | 苏州安侯医疗科技有限公司 | Anti-fog cleaning wet tissue and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
GB445182A (en) | 1936-03-30 |
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