US3657031A - Production of bonded nonwovens by the wet method - Google Patents
Production of bonded nonwovens by the wet method Download PDFInfo
- Publication number
- US3657031A US3657031A US837313A US3657031DA US3657031A US 3657031 A US3657031 A US 3657031A US 837313 A US837313 A US 837313A US 3657031D A US3657031D A US 3657031DA US 3657031 A US3657031 A US 3657031A
- Authority
- US
- United States
- Prior art keywords
- polymer
- carbon atoms
- aqueous medium
- fibers
- ammonium salt
- 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
- 238000000034 method Methods 0.000 title claims description 28
- 239000004745 nonwoven fabric Substances 0.000 title abstract description 15
- 238000004519 manufacturing process Methods 0.000 title description 7
- 229920000642 polymer Polymers 0.000 claims abstract description 52
- 239000000835 fiber Substances 0.000 claims abstract description 45
- 239000012736 aqueous medium Substances 0.000 claims abstract description 25
- 150000003839 salts Chemical class 0.000 claims abstract description 17
- 239000011230 binding agent Substances 0.000 claims abstract description 16
- 239000004753 textile Substances 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 150000003863 ammonium salts Chemical class 0.000 claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 35
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- -1 alkyl radicals Chemical class 0.000 claims description 16
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 14
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 12
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 9
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
- 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 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- 239000011591 potassium Substances 0.000 claims description 6
- 229910052708 sodium Inorganic materials 0.000 claims description 6
- 239000011734 sodium Substances 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 10
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 abstract description 7
- 238000001035 drying Methods 0.000 abstract description 4
- 238000001556 precipitation Methods 0.000 abstract description 2
- 238000000926 separation method Methods 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 description 21
- 239000006185 dispersion Substances 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- 229920001519 homopolymer Polymers 0.000 description 7
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 229920000058 polyacrylate Polymers 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 150000001991 dicarboxylic acids Chemical class 0.000 description 4
- 229920001567 vinyl ester resin Polymers 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- 229920002292 Nylon 6 Polymers 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 3
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 3
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- GNPSDJOWGWWXSS-UHFFFAOYSA-M 1-benzylpyridin-1-ium;chloride Chemical compound [Cl-].C=1C=CC=C[N+]=1CC1=CC=CC=C1 GNPSDJOWGWWXSS-UHFFFAOYSA-M 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- 229920002302 Nylon 6,6 Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 2
- 239000001530 fumaric acid Substances 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- BSSNZUFKXJJCBG-UPHRSURJSA-N (z)-but-2-enediamide Chemical compound NC(=O)\C=C/C(N)=O BSSNZUFKXJJCBG-UPHRSURJSA-N 0.000 description 1
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- YCUBDDIKWLELPD-UHFFFAOYSA-N ethenyl 2,2-dimethylpropanoate Chemical compound CC(C)(C)C(=O)OC=C YCUBDDIKWLELPD-UHFFFAOYSA-N 0.000 description 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- ADGJZVKOKVENDN-UHFFFAOYSA-N n-(butoxymethyl)-2-methylprop-2-enamide Chemical compound CCCCOCNC(=O)C(C)=C ADGJZVKOKVENDN-UHFFFAOYSA-N 0.000 description 1
- YOZHLACIXDCHPV-UHFFFAOYSA-N n-(methoxymethyl)-2-methylprop-2-enamide Chemical compound COCNC(=O)C(C)=C YOZHLACIXDCHPV-UHFFFAOYSA-N 0.000 description 1
- ULYOZOPEFCQZHH-UHFFFAOYSA-N n-(methoxymethyl)prop-2-enamide Chemical compound COCNC(=O)C=C ULYOZOPEFCQZHH-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000306 recurrent effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000004758 synthetic textile Substances 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
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical class OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
- D21H17/42—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
- D21H17/43—Carboxyl groups or derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/20—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing organic materials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/46—Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/603—Including strand or fiber material precoated with other than free metal or alloy
-
- 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.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/603—Including strand or fiber material precoated with other than free metal or alloy
- Y10T442/607—Strand or fiber material is synthetic polymer
Definitions
- natural or synthetic textile fibers are suspended in an aqueous medium and a bonding agent is added.
- the aqueous medium is then separated on a machine substantially resembling known paper machines and the structure is generally dried at elevated temperature.
- Fibers known as binder fibers for example of polyvinyl acetate or of cellulose loaded with polyacrylates, are often used as binders for bonding nonwovens.
- the webs of fibrous material thus acquire adequate wet tear resistance to enable them to the removed from the wire of the machine.
- the polyvinyl acetate fibers of the polyacrylates are softened so that the textile fibers are bonded together.
- the tear resistance of bonded nonwovens obtained by these known methods is however inadequate.
- the bonded nonwovens are often additionally impregnated with a plastics dispersion or solution.
- the handle of nonwovens prepared in this way is usually hard and similar to that of paper.
- paper and nonwovens can be prepared from fibers which have been treated successively with melamine resins or urea resins and an aqueous dispersion of a plasticized thermoplastic. If bonded nonwovens are prepared from such pretreated plastics by the wet method, products are obtained however from which the plasticizer can easily migrate. As a result, the handle becomes less good and in some cases the material becomes more prone to soiling.
- quaternary ammonium salts are particularly suitable which contain four identical or different alkyl, cycloalkyl and/or aralkyl radicals attached to a quaternary nitrogen atom, at least one of the radicals being an alkyl or aralkyl radical containing from seven to 20 carbon atoms.
- Linear or branched alkyl groups having one to 20 carbon atoms are of particular interest as the organic radicals of the quaternary ammonium salts.
- radicals are methyl, ethyl, n-propyl, isopropyl, n-butyl, tertiary-butyl, namyl, n-hexyl, 2-ethylhexyl, n-decyl, lauryl, stearyl and palmityl.
- the cyclohexyl radical is a particularly suitable cycloalkyl radical
- the benzyl radical is a particularly suitable aralkyl radical.
- Water-soluble quaternary ammonium salts which have four linear or branched alkyl groups having one to 20 carbon atoms of which one or two have seven to 20 carbon atoms, quaternary ammonium salts which have three linear or branched alkyl groups having one to 20 carbon atoms and one benzyl group and quaternary pyridinium salts which bear on the nitrogen atom a linear or branched alkyl group having seven to 20 carbon atoms or a benzyl radical are particularly suitable.
- the quaternary ammonium salts may be derived from any acids which are capable of forming quaternary ammonium salts provided the quaternary ammonium salts have adequate solubility in water.
- the salts of inorganic acids, especially chlorides and sulfates, are of particular interest. Specific examples of suitable quaternary ammonium salts are as follows:
- N,N,N-trimethyl-N-stearylammonium chloride N,N-dimethyl-N-stearyl-N-benzylammonium chloride
- N,N-dimethyl-N-lauryl-N-benzylammonium chloride and N- benzylpyridinium chloride are of special interest as quaternary ammonium salts.
- the quaternary ammonium salts may be added to the aqueous suspensions of the textile fibers in pure form, as suspensions in water, or, preferably, in the form of their concentrated aqueous solutions.
- Treatment of the fibers with the quaternary ammonium salts is generally carried out at room temperature and preferably while stirring. In special cases it may be advantageous to use temperatures which are above or below room temperature, for example at +50 C or +5 C.
- the temperature of the aqueous liquor is usually from 10 to 30 C.
- Treatment of the fibers with the quaternary ammonium salts usually requires from 15 to 30 minutes. In special cases, for example when elevated temperature is used, further processing may be commenced only a few minutes after addition of the quaternary ammonium salt to the suspension of fibers.
- Polymers of afi-olefinically unsaturated monocarboxylic acids containing three or four carbon atoms, such as acrylic and/or methacrylic acid, are preferred as water-soluble salts of homopolymers and copolymers containing carboxyl groups. They are preferably derived from caustic alkali solutions, such as caustic soda and caustic potash solutions, or ammonia. Other examples are copolymers of maleic acid, fumaric acid,
- the polymers may contain (in addition to the a,B-olefinically unsaturated monocarboxylic or dicarboxylic acids of the said type which preferably contain from three to five carbon atoms) copolymerized units of other olefinically unsaturated monomers, particularly esters of acrylic and/or methacrylic acid with lower alcohols, particularly alkanols containing one to four carbon atoms, such as methyl acrylate, methyl methacrylate, ethyl acrylate and nbutyl acrylate, vinyl esters, particularly vinyl acetate, afiolefinically unsaturated nitriles, particularly acrylonitrile, amides of a,a-olefinically unsaturated carboxylic acids and their derivatives, particularly acrylamide, methacrylamide, N- methylolmethacrylamide, N-methylolacrylamide, maleimide, maleamide, N-methoxy
- Suitable polymers containing carboxyl groups and the polymers of vinylpyrrolidone generally have K values of 20 to 80, preferably 30 to 60 (measured according to H. Fikentscher, Cellulosechemie, volume 13 (1932), page 58).
- the ratio of quaternary organic ammonium salt (solid) to water-soluble salt of polymer containing carboxyl groups (solid) or the vinyl pyrrolidone polymer (solid) is generally from 10:1 to 20:1, preferably from 13:1 to 17:1.
- Polymers suitable for the preparation of bonded nonwovens which are generally in the form of their aqueous dispersions, are suitable as binder polymers.
- Aqueous dispersions which contain from 40 to 60 percent by weight of acrylic ester and/or methacrylic ester polymers having carboxyl groups are particularly suitable.
- These polyacrylates are usually derived from esters of acrylic or methacrylic acid with alkanols containing from one to 12, particularly from one to eight, carbon atoms, which often form the major component of the copolymers.
- Such polyacrylates generally contain (as monomers having carboxyl groups) from 1 to 10 percent by weight of polymerized units of a,B-olefinically unsaturated monocarboxylic and/or dicarboxylic acids which preferably contain from three to five carbon atoms.
- the proportion of such olefinically unsaturated carboxylic acids in the copolymers is preferably from 2 to 5 percent by weight with reference to the copolymer.
- Acrylic and methacrylic acids are particularly suitable; crotonic acid, maleic acid, fumaric acid and itaconic acid are also suitable.
- the polyacrylates may additionally contain polymerized units of further olefinically unsaturated monomers, for example vinylaromatic compounds such as styrene, vinyl halides or vinylidene halides, such vinyl chloride and vinylidene chloride, acrylonitrile, methacrylonitrile and/or vinyl esters of saturated aliphatic monocarboxylic acids usually containing from two to 12 carbon atoms, such as vinyl acetate, vinyl propionate, vinyl laurate and vinyl pivalate and also (usually in amounts of from I to percent, particularly from 2 to 7 percent, by weight with reference to the copolymer) of amides of a,/3-olefinically unsaturated monocarboxylic and/or dicarboxylic acids usually containing from three to five carbon atoms or their derivatives, particularly acrylamide, methacrylamide, N- methylolacrylamide, N-methylolmethacrylamide, N-methoxymethylmethacrylamide and N-n-butoxymethyl
- binder polymers are aqueous dispersions based on polymers of vinyl chloride and/or vinylidene chloride, based on butadiene-styrene copolymers or butadiene-acrylonitrile copolymers and/or based on vinyl ester polymers, for example polymers of vinyl acetate or vinyl propionate, which may contain conventional anionic or nonionic emulsifiers with or without protective colloids.
- binder polymer in each case calculated as solids and with reference to the amount of textile fibers
- the amount of textile fibers (with reference to the amount of water) is usually from 0.5 to 3 percent, preferably from 0.7 to 1.5 percent, by weight, the fibers preferably being from 5 to mm in length.
- the textile fibers may consist for example of cellulose or cellulose derivatives, synthetic polyamides having recurrent CONl-l groups in the molecular chain, such as polycaprolactam or polyhexamethylene adipamide, saturated polyesters, such as polyethylene glycol terephthalate, or polyacrylonitrile.
- Additives conventionally used for finishing textiles and/or paper provided they are compatible with the other additives,
- aqueous medium may be used in the conventional way and if desired may be added to the aqueous medium.
- EXAMPLE 1 25 parts of rayon staple fibers having a denier of 1.7 and a length of from 1 to 10 mm is suspended in 2,500 parts of water and then 6 parts of a 54 percent aqueous solution of N-lauryl- N,N-dimethyl-N-benzylammonium chloride is added. The whole is stirred for 15 minutes and 2 parts of a 10 percent aqueous solution of a commercial copolymer (partly hydrolyzed with ammonia) of equal parts of methyl acrylate and acrylonitrile is gradually added.
- a commercial copolymer partially hydrolyzed with ammonia
- a 40 percent aqueous dispersion of a copolymer of 90 parts of n-butyl acrylate, 6 parts of acrylic acid and 4 parts of N-methylolmethacrylamide (which contains as an emulsifier 1.7 parts of a sulfonated oxyethylation product of n-nonylphenol which contains 18 to 20 ethylene oxide radicals and 0.3 part of Turkey red oil) is added.
- the binder polymer is deposited during stirring on the fibers within about 15 minutes.
- the aqueous fiber suspension is then introduced into an inclined wire web forming machine, the water is suction filtered, and the web is lifted off from the wire and dried at from 90 to 130 C.
- a nonwoven fabric is obtained which in the dry condition has a tensile strength of from 50 to kglcm measured according to DIN 53,112.
- the nonwoven has a soft textile handle. It is strongly fungicidal and bactericidal and is particularly suitable for hygienic disposable articles.
- EXAMPLE 2 20 parts of rayon staple fibers having a denier of 1.7 and a length of 10 mm is suspended in 2,000 parts of water and then 6 parts of a 50 percent aqueous solution of N-benzylpyridinium chloride is added to the suspension. The whole is stirred for about 15 minutes and then 1 part of a 20 percent aqueous solution of sodium polyacrylate (K value of the polyacrylic acid 30) is added. 40 parts of a 40 percent aqueous dispersion of a copolymer of parts of n-butyl acrylate, 5 parts of N-methylolacrylamide, 3 parts of 1,4-butanediol dimethacrylate and 7 parts of acrylic acid is then added.
- the binder polymer is deposited on the fibers during stirring.
- the aqueous suspension of the fibers is then fed to the wire section of a web forming machine, the water is sucked off as usual and the web is dried at from 120 to 140 C.
- a nonwoven is obtained which in the dry condition has a tensile strength of 54 kg/cm according to DIN 53,112.
- EXAMPLE 3 10 parts of polycaprolactam fibers having a denier of 3 and a length of 10 mm and 10 parts of rayon staple fibers having a denier of 1.5 and a length of 10 mm are suspended in 2,000 parts of water. 4 parts of a percent pasty suspension of N- stearyl-N,N-di-(a-hydroxyisopropyl)-N-methylammonium methosulfate is added to the suspension while stirring.
- EXAMPLE 4 20 parts of polycaprolactam fibers having a denier of 1.5 and a length of from 8 to 10 mm and 5 parts of polyhexamethylene adipamide fibers having a denier of 6 and a length of 32 mm are suspended in 2,500 parts of water. parts of N,N-distearyl-N,N-dimethylammonium chloride is then added as a concentrated aqueous solution and this quaternary ammonium salt is allowed to go on to the fibers for about 20 minutes while stirring.
- a concentrated aqueous solution of 2 parts of the ammonium salt of a copolymer of equal parts of acrylic acid and methacrylic acid prepared in the usual way is then added followed by 50 parts of a 50 percent aqueous dispersion, prepared in the usual way, of a copolymer of 93 parts of ethyl acrylate, 3 parts of acrylonitrile, 3 parts of N- methylolacrylamide and 1 part of acrylic acid.
- the binder polymer After the binder polymer has gone onto the fiber, the web is formed and dried as described in Example 1.
- a nonwoven is obtained which is suitable for example for the production of hygienic disposable articles.
- compound (A) is a quaternary ammonium salt, dissolved in the aqueous medium, which has four linear or branched alkyl radicals each having from one to 20 carbon atoms of which one or two have seven to 20 carbon atoms and polymer (B) is a water-soluble salt of a polymer of an afiolefinically unsaturated monocarboxylic or dicarboxylic acid containing from three to five carbon atoms.
- compound (A) is a quaternary ammonium salt, dissolved in the aqueous medium, which bears three linear or branched alkyl groups having from one to 20 carbon atoms and one benzyl group and polymer (B) is a water-soluble salt of a polymer of an a,B-olefinically unsaturated monocarboxylic or dicarboxylic acid containing from three to five carbon atoms.
- compound (A) is a quaternary pyridinium salt, dissolved in the aqueous medium, which bears on the nitrogen atom a linear or branched alkyl group having from seven to 20 carbon atoms or a benzyl radical and polymer (B) is a watersoluble salt of a polymer of an a,B-olefinically unsaturated monocarboxylic or dicarboxylic acid containing from three to five carbon atoms.
- polymer (B) is a potassium, sodium or ammonium salt of a polymer of an a,,B-olefmically unsaturated carboxylic acid containing from three to four carbon atoms.
- compound (A) is a quaternary salt, dissolved in the aqueous medium, which bears three linear or branched alkyl groups having from one to 20 carbon atoms and one benzyl group and polymer (B) is a potassium, sodium or ammonium salt of a polymer of acrylic acid or methacrylic acid.
- compound (A) is a quaternary ammonium salt which bears three linear or branched alkyl groups having from one to 20 carbon atoms and one benzyl group and polymer (B) is a potassium, sodium or ammonium salt of a polymer of acrylic acid or methacrylic acid.
- the amount of said binder being 5-50 percent by weight, calculated as solids, with reference to the textile fibers, and the amount of said textile fibers being 0.5 to 3 percent by weight, based on the water of said aqueous medium.
- the weight ratio of said quaternary ammonium salt to said polymer (B) being in the range of 10:1 to 20:1.
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Abstract
Textile nonwovens can be prepared with particular advantage by treatment of textile fibers suspended in an aqueous medium with dissolved quaternary organic ammonium salts and with watersoluble salts of polymers having carboxyl groups of vinylpyrrolidone polymers, precipitation of binder polymers dispersed in water onto the treated suspended fibers, separation of the aqueous medium from the fibers and drying the bonded fibers.
Description
llnited States Patent Reinhard et a1.
[ 3,657,631 [451 Apr. 18, 1972 PRODUCTION or BONDED NoNwovENs BY THE WET METHOD Inventors: Hans Reinhard, Limburgerhof; Gerhard Welzel, Mannheim; Hans-Ulrich Frank; Rudolf Stephan, both of Ludwigshafen, all of Germany Assignee: Badische Anilin- & Soda-Fabrik Aktiengesellschaft, Ludwigshafen am Rhine, Germany I 1 Filed: June 27, 1969 Appl. No.: 837,313
Foreign Application Priority Data June 29, 1968 Germany ..P 17 69 699.0
US. Cl ..l56/62.2,156/377,161/170 Int. Cl. ..B29j 5/00 Field ofSearch ..156/314, 181,287, 62.2,.377;
Relerences Cited UNITED STATES PATENTS 2,746,898 5/1956 Buckwalteretal. ..156/314X 2,932,598 4/1960 Henning ..l56/314X Primary Examiner-Carl C. Quarforth Assistant Examiner-Stephen J. Lechert, Jr. Attorney-Johnston, Root, OKeeffe, Keil, Thompson & Shurtleff [5 7] ABSTRACT 9 Claims, No Drawings PRODUCTION OF BONDED NONWOVENS BY THE WET METHOD This invention relates to a process for the production of bonded nonwovens by the wet method.
In the wet method for the production of bonded nonwoven fabrics, natural or synthetic textile fibers are suspended in an aqueous medium and a bonding agent is added. The aqueous medium is then separated on a machine substantially resembling known paper machines and the structure is generally dried at elevated temperature.
Fibers known as binder fibers, for example of polyvinyl acetate or of cellulose loaded with polyacrylates, are often used as binders for bonding nonwovens. The webs of fibrous material thus acquire adequate wet tear resistance to enable them to the removed from the wire of the machine. When drying and heating is carried out, the polyvinyl acetate fibers of the polyacrylates are softened so that the textile fibers are bonded together. The tear resistance of bonded nonwovens obtained by these known methods is however inadequate. For this reason, the bonded nonwovens are often additionally impregnated with a plastics dispersion or solution. However, the handle of nonwovens prepared in this way is usually hard and similar to that of paper.
It is furthermore known from British Pat. No. 1,071,136 that paper and nonwovens can be prepared from fibers which have been treated successively with melamine resins or urea resins and an aqueous dispersion of a plasticized thermoplastic. If bonded nonwovens are prepared from such pretreated plastics by the wet method, products are obtained however from which the plasticizer can easily migrate. As a result, the handle becomes less good and in some cases the material becomes more prone to soiling.
We have now found that the production of bonded nonwovens by the wet method by suspending textile fibers in an aqueous medium, precipitating a binder polymer dispersed in the aqueous medium onto the fibers, separating the aqueous medium and drying the nonwoven at elevated temperature can be advantageously carried out by first treating the fibers suspended in the aqueous medium with a quaternary ammonium salt dissolved in the aqueous medium which has at least one alkyl or aralkyl group containing from seven to 20 carbon atoms, and adding to the suspension of the fibers a water-soluble salt of a homopolymer and/or copolymer containing carboxyl groups and/or a water-soluble homopolymer and/or copolymer of vinylpyrrolidone and then adding an aqueous dispersion of the binder polymer.
Those quaternary ammonium salts are particularly suitable which contain four identical or different alkyl, cycloalkyl and/or aralkyl radicals attached to a quaternary nitrogen atom, at least one of the radicals being an alkyl or aralkyl radical containing from seven to 20 carbon atoms. Linear or branched alkyl groups having one to 20 carbon atoms are of particular interest as the organic radicals of the quaternary ammonium salts. Specific examples of such radicals are methyl, ethyl, n-propyl, isopropyl, n-butyl, tertiary-butyl, namyl, n-hexyl, 2-ethylhexyl, n-decyl, lauryl, stearyl and palmityl. The cyclohexyl radical is a particularly suitable cycloalkyl radical, and the benzyl radical is a particularly suitable aralkyl radical. Water-soluble quaternary ammonium salts which have four linear or branched alkyl groups having one to 20 carbon atoms of which one or two have seven to 20 carbon atoms, quaternary ammonium salts which have three linear or branched alkyl groups having one to 20 carbon atoms and one benzyl group and quaternary pyridinium salts which bear on the nitrogen atom a linear or branched alkyl group having seven to 20 carbon atoms or a benzyl radical are particularly suitable. The quaternary ammonium salts may be derived from any acids which are capable of forming quaternary ammonium salts provided the quaternary ammonium salts have adequate solubility in water. The salts of inorganic acids, especially chlorides and sulfates, are of particular interest. Specific examples of suitable quaternary ammonium salts are as follows:
N,N,N-trimethyl-N-stearylammonium chloride, N,N-dimethyl-N-stearyl-N-benzylammonium chloride,
and
N,N-dimethyl-N-lauryl-N-benzylammonium chloride and N- benzylpyridinium chloride are of special interest as quaternary ammonium salts.
The quaternary ammonium salts may be added to the aqueous suspensions of the textile fibers in pure form, as suspensions in water, or, preferably, in the form of their concentrated aqueous solutions. Treatment of the fibers with the quaternary ammonium salts is generally carried out at room temperature and preferably while stirring. In special cases it may be advantageous to use temperatures which are above or below room temperature, for example at +50 C or +5 C. The temperature of the aqueous liquor is usually from 10 to 30 C. Treatment of the fibers with the quaternary ammonium salts usually requires from 15 to 30 minutes. In special cases, for example when elevated temperature is used, further processing may be commenced only a few minutes after addition of the quaternary ammonium salt to the suspension of fibers.
Polymers of afi-olefinically unsaturated monocarboxylic acids containing three or four carbon atoms, such as acrylic and/or methacrylic acid, are preferred as water-soluble salts of homopolymers and copolymers containing carboxyl groups. They are preferably derived from caustic alkali solutions, such as caustic soda and caustic potash solutions, or ammonia. Other examples are copolymers of maleic acid, fumaric acid,
itaconic acid and/or crotonic acid. The polymers may contain (in addition to the a,B-olefinically unsaturated monocarboxylic or dicarboxylic acids of the said type which preferably contain from three to five carbon atoms) copolymerized units of other olefinically unsaturated monomers, particularly esters of acrylic and/or methacrylic acid with lower alcohols, particularly alkanols containing one to four carbon atoms, such as methyl acrylate, methyl methacrylate, ethyl acrylate and nbutyl acrylate, vinyl esters, particularly vinyl acetate, afiolefinically unsaturated nitriles, particularly acrylonitrile, amides of a,a-olefinically unsaturated carboxylic acids and their derivatives, particularly acrylamide, methacrylamide, N- methylolmethacrylamide, N-methylolacrylamide, maleimide, maleamide, N-methoxymethylacrylamide and N-methoxymethylrnethacrylamide, vinyl esters of lower fatty acids, particularly vinyl acetate, vinyl and vinylidene halides, particularly vinyl chloride, and vinylaromatic compounds, particularly styrene. The proportion of such comonomers may be varied within wide limits, practically the only limitation being the requirement that the salts of the copolymers should have adequate solubility in water.
It is possible in the new process to use water-soluble homopolymers and/or copolymers of vinylpyrrolidone instead of or together with the salts of homopolymers and/or copolymers containing carboxyl groups. In addition to the comonomers specified in the preceding paragraph, afiolefinically unsaturated monocarboxylic and/or dicarboxylic acids, particularly acrylic acid, methacrylic acid and maleic acid, may be used as comonomers for vinylpyrrolidone. The carboxyl groups may also be introduced into the polymers by complete or partial hydrolysis of comonomers such as acrylonitrile or acrylamide. Suitable polymers containing carboxyl groups and the polymers of vinylpyrrolidone generally have K values of 20 to 80, preferably 30 to 60 (measured according to H. Fikentscher, Cellulosechemie, volume 13 (1932), page 58).
The ratio of quaternary organic ammonium salt (solid) to water-soluble salt of polymer containing carboxyl groups (solid) or the vinyl pyrrolidone polymer (solid) is generally from 10:1 to 20:1, preferably from 13:1 to 17:1.
Polymers suitable for the preparation of bonded nonwovens, which are generally in the form of their aqueous dispersions, are suitable as binder polymers. Aqueous dispersions which contain from 40 to 60 percent by weight of acrylic ester and/or methacrylic ester polymers having carboxyl groups are particularly suitable. These polyacrylates are usually derived from esters of acrylic or methacrylic acid with alkanols containing from one to 12, particularly from one to eight, carbon atoms, which often form the major component of the copolymers. Such polyacrylates generally contain (as monomers having carboxyl groups) from 1 to 10 percent by weight of polymerized units of a,B-olefinically unsaturated monocarboxylic and/or dicarboxylic acids which preferably contain from three to five carbon atoms. The proportion of such olefinically unsaturated carboxylic acids in the copolymers is preferably from 2 to 5 percent by weight with reference to the copolymer. Acrylic and methacrylic acids are particularly suitable; crotonic acid, maleic acid, fumaric acid and itaconic acid are also suitable. The polyacrylates may additionally contain polymerized units of further olefinically unsaturated monomers, for example vinylaromatic compounds such as styrene, vinyl halides or vinylidene halides, such vinyl chloride and vinylidene chloride, acrylonitrile, methacrylonitrile and/or vinyl esters of saturated aliphatic monocarboxylic acids usually containing from two to 12 carbon atoms, such as vinyl acetate, vinyl propionate, vinyl laurate and vinyl pivalate and also (usually in amounts of from I to percent, particularly from 2 to 7 percent, by weight with reference to the copolymer) of amides of a,/3-olefinically unsaturated monocarboxylic and/or dicarboxylic acids usually containing from three to five carbon atoms or their derivatives, particularly acrylamide, methacrylamide, N- methylolacrylamide, N-methylolmethacrylamide, N-methoxymethylmethacrylamide and N-n-butoxymethylmethacrylamide, and vinylsulfonic acids and their salts. The aqueous dispersion of such polyacrylates may contain the usual amounts of conventional anionic and/or nonionic emulsifiers with or without small amounts of protective colloids.
Other suitable binder polymers are aqueous dispersions based on polymers of vinyl chloride and/or vinylidene chloride, based on butadiene-styrene copolymers or butadiene-acrylonitrile copolymers and/or based on vinyl ester polymers, for example polymers of vinyl acetate or vinyl propionate, which may contain conventional anionic or nonionic emulsifiers with or without protective colloids.
Generally from 5 to 50 percent, preferably from 15 to 35 percent, by weight of binder polymer (in each case calculated as solids and with reference to the amount of textile fibers) are used in the new process.
The amount of textile fibers (with reference to the amount of water) is usually from 0.5 to 3 percent, preferably from 0.7 to 1.5 percent, by weight, the fibers preferably being from 5 to mm in length. The textile fibers may consist for example of cellulose or cellulose derivatives, synthetic polyamides having recurrent CONl-l groups in the molecular chain, such as polycaprolactam or polyhexamethylene adipamide, saturated polyesters, such as polyethylene glycol terephthalate, or polyacrylonitrile.
Additives conventionally used for finishing textiles and/or paper, provided they are compatible with the other additives,
may be used in the conventional way and if desired may be added to the aqueous medium.
The invention is illustrated by the following Examples, in which parts and percentages are by weight.
EXAMPLE 1 25 parts of rayon staple fibers having a denier of 1.7 and a length of from 1 to 10 mm is suspended in 2,500 parts of water and then 6 parts of a 54 percent aqueous solution of N-lauryl- N,N-dimethyl-N-benzylammonium chloride is added. The whole is stirred for 15 minutes and 2 parts of a 10 percent aqueous solution of a commercial copolymer (partly hydrolyzed with ammonia) of equal parts of methyl acrylate and acrylonitrile is gradually added. Then 60 parts of a 40 percent aqueous dispersion of a copolymer of 90 parts of n-butyl acrylate, 6 parts of acrylic acid and 4 parts of N-methylolmethacrylamide (which contains as an emulsifier 1.7 parts of a sulfonated oxyethylation product of n-nonylphenol which contains 18 to 20 ethylene oxide radicals and 0.3 part of Turkey red oil) is added. The binder polymer is deposited during stirring on the fibers within about 15 minutes. The aqueous fiber suspension is then introduced into an inclined wire web forming machine, the water is suction filtered, and the web is lifted off from the wire and dried at from 90 to 130 C.
A nonwoven fabric is obtained which in the dry condition has a tensile strength of from 50 to kglcm measured according to DIN 53,112. The nonwoven has a soft textile handle. It is strongly fungicidal and bactericidal and is particularly suitable for hygienic disposable articles.
EXAMPLE 2 20 parts of rayon staple fibers having a denier of 1.7 and a length of 10 mm is suspended in 2,000 parts of water and then 6 parts of a 50 percent aqueous solution of N-benzylpyridinium chloride is added to the suspension. The whole is stirred for about 15 minutes and then 1 part of a 20 percent aqueous solution of sodium polyacrylate (K value of the polyacrylic acid 30) is added. 40 parts of a 40 percent aqueous dispersion of a copolymer of parts of n-butyl acrylate, 5 parts of N-methylolacrylamide, 3 parts of 1,4-butanediol dimethacrylate and 7 parts of acrylic acid is then added. The binder polymer is deposited on the fibers during stirring. The aqueous suspension of the fibers is then fed to the wire section of a web forming machine, the water is sucked off as usual and the web is dried at from 120 to 140 C. A nonwoven is obtained which in the dry condition has a tensile strength of 54 kg/cm according to DIN 53,112.
EXAMPLE 3 10 parts of polycaprolactam fibers having a denier of 3 and a length of 10 mm and 10 parts of rayon staple fibers having a denier of 1.5 and a length of 10 mm are suspended in 2,000 parts of water. 4 parts of a percent pasty suspension of N- stearyl-N,N-di-(a-hydroxyisopropyl)-N-methylammonium methosulfate is added to the suspension while stirring. Stirring is continued for about another half hour and then 2 parts of a 10 percent aqueous solution of a copolymer (neutralized with ammonia) of 70 parts of acrylic acid, 20 parts of methacrylamide, 5 parts of acrylonitrile and 5 parts of ethyl acrylate, and 30 parts of a 50 percent aqueous dispersion of a copolymer of 55 parts of n-butyl acrylate, 45 parts of vinyl acetate and 2 parts of acrylic acid are then added in the sequence given. After the lastmentioned binder polymer has been deposited on the fibers, the web is formed as described in Example 1 and dried at from to C. The nonwoven obtained has a srfft textile handle and is suitable for hygienic disposable artic es.
EXAMPLE 4 20 parts of polycaprolactam fibers having a denier of 1.5 and a length of from 8 to 10 mm and 5 parts of polyhexamethylene adipamide fibers having a denier of 6 and a length of 32 mm are suspended in 2,500 parts of water. parts of N,N-distearyl-N,N-dimethylammonium chloride is then added as a concentrated aqueous solution and this quaternary ammonium salt is allowed to go on to the fibers for about 20 minutes while stirring. A concentrated aqueous solution of 2 parts of the ammonium salt of a copolymer of equal parts of acrylic acid and methacrylic acid prepared in the usual way is then added followed by 50 parts of a 50 percent aqueous dispersion, prepared in the usual way, of a copolymer of 93 parts of ethyl acrylate, 3 parts of acrylonitrile, 3 parts of N- methylolacrylamide and 1 part of acrylic acid. After the binder polymer has gone onto the fiber, the web is formed and dried as described in Example 1. A nonwoven is obtained which is suitable for example for the production of hygienic disposable articles.
We claim:
1. In a process for the production of bonded nonwovens by the wet method by suspending textile fibers in an aqueous medium, impregnating the suspended fibers by precipitation thereon of a binder polymer dispersed in the aqueous medium, separating the aqueous medium from the impregnated fibers and forming a web of said impregnated fibers, and drying the impregnated fiber web at elevated temperature, the improvement which comprises adding to the suspension of the fibers in the aqueous medium, prior to said impregnating with the binder polymer, (A) a quaternary ammonium salt, dissolved in the aqueous medium, which has at least one alkyl or aralkyl group containing from seven to 20 carbon atoms and (B) at least one of a water-soluble salt of a homopolymer or copolymer containing carboxyl groups or a water-soluble homopolymer or copolymer of vinyl-pyrrolidone.
2. In a process as claimed in claim 1 the improvement wherein compound (A) is a quaternary ammonium salt, dissolved in the aqueous medium, which has four linear or branched alkyl radicals each having from one to 20 carbon atoms of which one or two have seven to 20 carbon atoms and polymer (B) is a water-soluble salt of a polymer of an afiolefinically unsaturated monocarboxylic or dicarboxylic acid containing from three to five carbon atoms.
3. In a process as claimed in claim 1, the improvement wherein compound (A) is a quaternary ammonium salt, dissolved in the aqueous medium, which bears three linear or branched alkyl groups having from one to 20 carbon atoms and one benzyl group and polymer (B) is a water-soluble salt of a polymer of an a,B-olefinically unsaturated monocarboxylic or dicarboxylic acid containing from three to five carbon atoms.
4. In a process as claimed in claim 1, the improvement wherein compound (A) is a quaternary pyridinium salt, dissolved in the aqueous medium, which bears on the nitrogen atom a linear or branched alkyl group having from seven to 20 carbon atoms or a benzyl radical and polymer (B) is a watersoluble salt of a polymer of an a,B-olefinically unsaturated monocarboxylic or dicarboxylic acid containing from three to five carbon atoms.
5. In a process as claimed in claim 1, the improvement wherein polymer (B) is a potassium, sodium or ammonium salt of a polymer of an a,,B-olefmically unsaturated carboxylic acid containing from three to four carbon atoms.
6. In process as claimed in claim 1, the improvement wherein compound (A) is a quaternary salt, dissolved in the aqueous medium, which bears three linear or branched alkyl groups having from one to 20 carbon atoms and one benzyl group and polymer (B) is a potassium, sodium or ammonium salt of a polymer of acrylic acid or methacrylic acid.
7. In a process as claimed in claim 1 the improvement wherein compound (A) is a quaternary ammonium salt which bears three linear or branched alkyl groups having from one to 20 carbon atoms and one benzyl group and polymer (B) is a potassium, sodium or ammonium salt of a polymer of acrylic acid or methacrylic acid.
. In a process as claimed in clau'n 1, the amount of said binder being 5-50 percent by weight, calculated as solids, with reference to the textile fibers, and the amount of said textile fibers being 0.5 to 3 percent by weight, based on the water of said aqueous medium.
9. In a process as claimed in claim 1, the weight ratio of said quaternary ammonium salt to said polymer (B) being in the range of 10:1 to 20:1.
Claims (8)
- 2. In a process as claimed in claim 1 the improvement wherein compound (A) is a quaternary ammonium salt, dissolved in the aqueous medium, which has four linear or branched alkyl radicals each having from one to 20 carbon atoms of which one or two have seven to 20 carbon atoms and polymer (B) is a water-soluble salt of a polymer of an Alpha , Beta -olefinically unsaturated monocarboxylic or dicarboxylic acid containing from three to five carbon atoms.
- 3. In a process as claimed in claim 1, the improvement wherein compound (A) is a quaternary ammonium salt, dissolved in the aqueous medium, which bears three linear or branched alkyl groups having from one to 20 carbon atoms and one benzyl group and polymer (B) is a water-soluble salt of a polymer of an Alpha , Beta -olefinically unsaturated monocarboxylic or dicarboxylic acid containing from three to five carbon atoms.
- 4. In a process as claimed in claim 1, the improvement wherein compound (A) is a quaternary pyridinium salt, dissolved in the aqueous medium, which bears on the nitrogen atom a linear or branched alkyl group having from seven to 20 carbon atoms or a benzyl radical and polymer (B) is a water-soluble salt of a polymer of an Alpha , Beta -olefinically unsaturated monocarboxylic or dicarboxylic acid containing from three to five carbon atoms.
- 5. In a process as claimed in claim 1, the improvement wherein polymer (B) is a potassium, sodium or ammonium salt of a polymer of an Alpha , Beta -olefinically unsaturated carboxylic acid containing from three to four carbon atoms.
- 6. In process as claimed in claim 1, the improvement wherein compound (A) is a quaternary salt, dissolved in the aqueous medium, which bears three linear or branched alkyl groups having from one to 20 carbon atoms and one benzyl group and polymer (B) is a potassium, sodium or ammonium salt of a polymer of acrylic acid or methacrylic acid.
- 7. In a process as claimed in claim 1 the improvement wherein compound (A) is a quaternary ammonium salt which bears three linear or branched alkyl groups having from one to 20 carbon atoms and one benzyl group and polymer (B) is a potassium, sodium or ammonium salt of a polymer of acrylic acid or methacrylic acid.
- 8. In a process as claimed in claim 1, the amount of said binder being 5-50 percent by weight, calculated as solids, with reference to the textile fibers, and the amount of said textile fibers being 0.5 to 3 percent by weight, based on the water of said aqueous medium.
- 9. In a process as claimed in claim 1, the weight ratio of said quaternary ammonium salt to said polymer (B) being in the range of 10:1 to 20:1.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19681769699 DE1769699A1 (en) | 1968-06-29 | 1968-06-29 | Process for the production of bonded nonwovens by the wet process |
Publications (1)
Publication Number | Publication Date |
---|---|
US3657031A true US3657031A (en) | 1972-04-18 |
Family
ID=5700230
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US837313A Expired - Lifetime US3657031A (en) | 1968-06-29 | 1969-06-27 | Production of bonded nonwovens by the wet method |
Country Status (6)
Country | Link |
---|---|
US (1) | US3657031A (en) |
AT (1) | AT291928B (en) |
DE (1) | DE1769699A1 (en) |
FR (1) | FR2014443A1 (en) |
GB (1) | GB1263098A (en) |
NL (1) | NL6909844A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040098655A1 (en) * | 2002-11-19 | 2004-05-20 | Sharma Debendra Das | Rolling CRC scheme for improved error detection |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1090511A (en) * | 1975-05-02 | 1980-12-02 | Vincent M. Rasicci | Method for controlling canadian standard freeness in fiber slurry beater addition |
US4319956A (en) * | 1980-06-16 | 1982-03-16 | The Dexter Corporation | Nonwoven web material for medical towels and the like |
GB8811955D0 (en) * | 1988-05-20 | 1988-06-22 | Allied Colloids Ltd | Absorbent products & their manufacture |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2746898A (en) * | 1953-10-29 | 1956-05-22 | Us Rubber Co | Dry adhesion method for adhering textile material to rubber |
US2932598A (en) * | 1954-08-12 | 1960-04-12 | Bjorksten Res Lab Inc | Glass fiber treatment |
-
1968
- 1968-06-29 DE DE19681769699 patent/DE1769699A1/en active Pending
-
1969
- 1969-06-26 AT AT606669A patent/AT291928B/en not_active IP Right Cessation
- 1969-06-26 NL NL6909844A patent/NL6909844A/xx unknown
- 1969-06-26 GB GB32353/69A patent/GB1263098A/en not_active Expired
- 1969-06-27 US US837313A patent/US3657031A/en not_active Expired - Lifetime
- 1969-06-27 FR FR6921736A patent/FR2014443A1/fr not_active Withdrawn
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2746898A (en) * | 1953-10-29 | 1956-05-22 | Us Rubber Co | Dry adhesion method for adhering textile material to rubber |
US2932598A (en) * | 1954-08-12 | 1960-04-12 | Bjorksten Res Lab Inc | Glass fiber treatment |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20040098655A1 (en) * | 2002-11-19 | 2004-05-20 | Sharma Debendra Das | Rolling CRC scheme for improved error detection |
Also Published As
Publication number | Publication date |
---|---|
NL6909844A (en) | 1969-12-31 |
DE1769699A1 (en) | 1971-11-04 |
AT291928B (en) | 1971-08-10 |
FR2014443A1 (en) | 1970-04-17 |
GB1263098A (en) | 1972-02-09 |
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