EP0193107B1 - Gebundenes textiles Flächengebilde und Verfahren zu seiner Herstellung - Google Patents
Gebundenes textiles Flächengebilde und Verfahren zu seiner Herstellung Download PDFInfo
- Publication number
- EP0193107B1 EP0193107B1 EP86102172A EP86102172A EP0193107B1 EP 0193107 B1 EP0193107 B1 EP 0193107B1 EP 86102172 A EP86102172 A EP 86102172A EP 86102172 A EP86102172 A EP 86102172A EP 0193107 B1 EP0193107 B1 EP 0193107B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- bonded
- binder
- weight
- fibre fleece
- dispersion
- 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
- 239000004753 textile Substances 0.000 title claims description 17
- 238000000034 method Methods 0.000 title claims description 13
- 239000004744 fabric Substances 0.000 title description 17
- 238000004519 manufacturing process Methods 0.000 title description 7
- 239000000835 fiber Substances 0.000 claims description 26
- 239000006185 dispersion Substances 0.000 claims description 25
- 239000011230 binding agent Substances 0.000 claims description 22
- 229920001577 copolymer Polymers 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 11
- 229920002994 synthetic fiber Polymers 0.000 claims description 11
- NEYTXADIGVEHQD-UHFFFAOYSA-N 2-hydroxy-2-(prop-2-enoylamino)acetic acid Chemical compound OC(=O)C(O)NC(=O)C=C NEYTXADIGVEHQD-UHFFFAOYSA-N 0.000 claims description 10
- 229920000728 polyester Polymers 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000005250 alkyl acrylate group Chemical group 0.000 claims 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000012209 synthetic fiber Substances 0.000 description 7
- 239000004745 nonwoven fabric Substances 0.000 description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 4
- 239000012935 ammoniumperoxodisulfate Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- TXPYHRFTMYVSLD-UHFFFAOYSA-N 2,3,4-tris(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC=C(O)C(CC(C)C)=C1CC(C)C TXPYHRFTMYVSLD-UHFFFAOYSA-N 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000007596 consolidation process Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- -1 hydroxyalkyl ester Chemical class 0.000 description 2
- 125000005395 methacrylic acid group Chemical group 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 238000010992 reflux Methods 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 1
- UGGUVAUCPDITAU-UHFFFAOYSA-N 2-methoxy-2-(prop-2-enoylamino)propanoic acid Chemical compound COC(C)(C(O)=O)NC(=O)C=C UGGUVAUCPDITAU-UHFFFAOYSA-N 0.000 description 1
- RUPRLZZWRJIWKR-UHFFFAOYSA-N 2-methoxy-3-(prop-2-enoylamino)propanoic acid Chemical compound COC(CNC(=O)C=C)C(O)=O RUPRLZZWRJIWKR-UHFFFAOYSA-N 0.000 description 1
- TURITJIWSQEMDB-UHFFFAOYSA-N 2-methyl-n-[(2-methylprop-2-enoylamino)methyl]prop-2-enamide Chemical compound CC(=C)C(=O)NCNC(=O)C(C)=C TURITJIWSQEMDB-UHFFFAOYSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 244000104272 Bidens pilosa Species 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/435—Polyesters
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/425—Cellulose series
- D04H1/4258—Regenerated cellulose series
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
- D04H1/64—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
- D04H1/645—Impregnation followed by a solidification process
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/013—Regenerated cellulose series
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
- D04H3/12—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with filaments or yarns secured together by chemical or thermo-activatable bonding agents, e.g. adhesives, applied or incorporated in liquid or solid form
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/913—Material designed to be responsive to temperature, light, moisture
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2861—Coated or impregnated synthetic organic fiber fabric
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2861—Coated or impregnated synthetic organic fiber fabric
- Y10T442/291—Coated or impregnated polyolefin fiber fabric
Definitions
- the invention relates to a method for producing bound textile fabrics by applying an acrylic resin dispersion which is free of formaldehyde and formaldehyde-releasing substances.
- the invention further relates to the textile fabrics produced by the method.
- Aqueous acyl resin dispersions whose plastic content contained self-crosslinking amide methylol groups have hitherto been used frequently for the production of bound textile fabrics which are notable for high wet strength and for water and wash liquor resistance.
- binders for textile fabrics which provide sufficient wet strength, water and wash liquor resistance for practical purposes, but do not give off any formaldehyde when heated.
- EP-A 19 169 describes aqueous dispersions which are suitable as binders for nonwoven fabrics and which contain, as binders, a copolymer of acrylic or methacrylic esters or other monomers and 3 to 10% by weight of units of acrylamidoglycolic acid. It is therefore a binder that does not release formaldehyde when heated. However, since the desired wet strength of the textile fabrics finished with them is not achieved with these binders, small proportions of N-methylolacrylamide are polymerized into the copolymers, thereby increasing the wet strength of the finished fiber structures. however, the risk of formaldehyde release occurs again.
- EP-A 96 230 describes coating compositions which contain, as self-crosslinking binders, copolymers of acrylic monomers and a crosslinking system composed of methyl acrylamido-glycolic acid methyl ether and hydroxyl, carboxy or amido-functional comonomers. When heated, condensation reactions of the monomer units, the crosslinker system mentioned, occur. It is not known to use such copolymers as binders for textile fabrics.
- the invention has for its object to produce bonded fabrics with improved wet strength, from whose binder no formaldehyde is released when heated.
- the bonded fabrics made according to the invention are distinguished from those with conventional formaldehyde-free binders by a significantly increased wet strength. This is important in cases where the bound textile fabric is exposed to mechanical stress during manufacture, further processing or when used in the wet state.
- a typical application is the production of bonded nonwovens based on synthetic fibers, in particular polyester fibers, which are used for the production of so-called disposable diapers.
- the bonded non-woven fabrics form the outer cover of the diaper, which envelops a highly absorbent filler. Due to the low water absorption of the synthetic fibers, the outer shell still appears relatively dry when the coated insert has absorbed considerable amounts of liquid. However, it is essential that the outer casing does not tear under mechanical stress and exposes the liquid-saturated insert.
- the increased wet strength of the textile fabrics bound in the sense of the invention is based on the units of an acrylamidoglycolic acid monomer of the formula as a component of the copolymer contained in the aqueous dispersion.
- R, R 'and R'' have the meaning given in claim 1.
- R 'and R'' can be the same alkyl radicals, especially methyl groups.
- other alkyl radicals with preferably no more than 8 carbon atoms are also suitable, in particular lower alkyl radicals with up to 4 carbon atoms.
- the acrylic or methacrylic acid alkyl esters forming the main part of the copolymer, or their mixture with styrene, are selected in a manner known per se so that the dynamic freezing temperature T 1max is not more than 60 °, preferably not more than 20 ° C.
- the copolymer consists of 30 to 60 wt .-% of monomer units that give hard homopolymers, such as methyl, ethyl, propyl, isopropyl methacrylate or styrene, and about 20 to 70% acrylic acid esters of C1 ⁇ 8 alkanols or methacrylic acid esters of C4 ⁇ 8 alkanols.
- Unsaturated carboxylic acids such as acrylic or methacrylic acid are suitable as further monomer components Amounts of about 1% by weight improve the stability of the dispersion.
- Crosslinking comonomers such as glycol dimethacrylate, allyl methacrylate, methylene-bis-methacrylamide or butanediol diacrylate, can also improve the strength properties of the binder in small amounts. Too high a proportion of crosslinking agents would interfere with the film formation process and should therefore be avoided.
- the comonomers which can also be used also include acrylonitrile and methacrylonitrile, vinyl acetate, vinyl chloride, vinylidene chloride and others. Hydroxyesters and amides of acrylic or methacrylic acid are generally not present in the copolymers.
- the acrylic resin dispersions can be prepared by all common methods of emulsion polymerization. They can contain anionic, cationic or non-ionic emulsifiers or compatible mixtures thereof. They are expediently produced with solids contents of 50 to 70% by weight.
- the method of the invention is suitable for binding and solidifying textile fabrics of all kinds; these include woven fabrics, knitted fabrics, wadding and in particular non-woven nonwovens.
- the invention is not restricted to certain types of fibers, but synthetic fibers or fiber mixtures containing synthetic fibers are fundamentally preferred. These mixtures can contain, for example, 70% or more of synthetic fibers.
- the synthetic fibers considered include fibers made from regenerated cellulose, such as rayon or rayon, and in particular fully synthetic fibers, such as polyester or polypropylene fibers.
- Preferred textile fabrics are constructed from 70 to 100% by weight of polyester fibers and 0 to 30% by weight of cellulose.
- the preparation of the dispersion for the consolidation of fiber structures depends on the application process and the requirements placed on the end product.
- the additives used in these processes like wetting agents. Anti-foaming agents, thermosensitizers. Plasticizers and smoothing agents. Antistatic. Antimicrobials. Dyes, fillers, flame retardants, fragrances, etc. can also be used.
- the dispersions are diluted with water to a binder content of 10 to 40 percent by weight.
- the viscosity of the diluted dispersion can range from 10 to 10,000 mPa.s.
- For the consolidation of wadding for example made of polyester, polyamide or polyacrylonitrile fibers, an approximately 15 to 25% liquor is sprayed on.
- Compact nonwovens and needle felts can be solidified well by impregnation with 10 to 40% liquors and subsequent squeezing and drying.
- Light fiber fleeces can also be consolidated by foam impregnation; To do this, foaming agents and foam stabilizers are added to the approximately 10 to 25% dispersion and foamed with air up to a liter weight of 100 to 300 g. The impregnation is expediently carried out on the horizontal foulard.
- Very light non-woven fabrics can be partially solidified by printing with pastes that contain 20 to 40% binder and are adjusted to a viscosity of 4000 to 8000 mPa.s. Needle felts for high-quality floor and wall coverings are preferably splashed with thickened, possibly foamed liquors. Finally, nonwoven bonding is also possible by brushing.
- the solidified fiber structures generally contain between 5 and 100%, based on the fiber weight, of binder.
- the preferred binder content is between 10 and 30% by weight.
- the fiber structures equipped according to the invention obtain their favorable application properties only by drying at dryer temperatures above 110 ° to about 200 °, preferably in the range between 120 and 160 ° C.
- a crosslinking agent for example glyoxal, can be added to the dispersion.
- thermally pre-consolidated polyester fleece with a weight per unit area of approx. 18 g per m2 is impregnated with the plastic dispersion diluted to approx. 25% dry matter, excess dispersion squeezed out with the padding so that a resin coating of approx. 15% is achieved.
- the damp fleece is dried in the stenter at 140 ° C for 5 minutes.
- the breaking resistance is determined according to DIN 53 857, Part 2 on dry fleece (F) and on wet fleece (F n ) after 1 hour of water storage in the middle of a tensile testing machine that corresponds to DIN 51 221.
- a chromatography paper No. 1, Whatman
- the breaking resistance is determined according to DIN 53 112, sheets 1 and 2.
- Example 1 illustrates the invention using dispersion A.
- Example 2 is a comparative test with comparative dispersion B which was not prepared according to the teaching of the invention.
- Example 3 is a comparison test according to DE-OS 32 02 122.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Nonwoven Fabrics (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Materials For Medical Uses (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19853507154 DE3507154A1 (de) | 1985-02-28 | 1985-02-28 | Gebundenes textiles flaechengebilde und verfahren zu seiner herstellung |
DE3507154 | 1985-02-28 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0193107A2 EP0193107A2 (de) | 1986-09-03 |
EP0193107A3 EP0193107A3 (en) | 1989-07-19 |
EP0193107B1 true EP0193107B1 (de) | 1992-04-22 |
Family
ID=6263831
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86102172A Expired - Lifetime EP0193107B1 (de) | 1985-02-28 | 1986-02-19 | Gebundenes textiles Flächengebilde und Verfahren zu seiner Herstellung |
Country Status (7)
Country | Link |
---|---|
US (1) | US4689264A (enrdf_load_stackoverflow) |
EP (1) | EP0193107B1 (enrdf_load_stackoverflow) |
JP (1) | JPS61201061A (enrdf_load_stackoverflow) |
DE (2) | DE3507154A1 (enrdf_load_stackoverflow) |
DK (1) | DK165844C (enrdf_load_stackoverflow) |
FI (1) | FI84188C (enrdf_load_stackoverflow) |
NO (1) | NO164181C (enrdf_load_stackoverflow) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3734752A1 (de) * | 1987-10-14 | 1989-05-03 | Basf Ag | Verfahren zur herstellung von waessrigen (meth)acrylsaeureester-copolymer-dispersionen in zwei stufen und deren verwendung als impraegnier-, ueberzugs- und bindemittel fuer flaechige fasergebilde |
US5369204A (en) * | 1991-11-01 | 1994-11-29 | Cytec Technology Corp. | Low molecular weight acrylamidoglycolate crosslinker and process |
US5407728A (en) * | 1992-01-30 | 1995-04-18 | Reeves Brothers, Inc. | Fabric containing graft polymer thereon |
US5486210A (en) | 1992-01-30 | 1996-01-23 | Reeves Brothers, Inc. | Air bag fabric containing graft polymer thereon |
CN1044269C (zh) * | 1993-06-02 | 1999-07-21 | 美国3M公司 | 非织造制品及其制造方法 |
DE4344149A1 (de) * | 1993-12-23 | 1995-06-29 | Basf Ag | Formaldehydfreie wäßrige Kunstharzdispersionen |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2920377A1 (de) * | 1979-05-19 | 1980-12-04 | Basf Ag | Binde-, impraegnier- und ueberzugsmittel auf basis einer waessrigen dispersion eines amidgruppenhaltigen copolymerisats |
CA1135712A (en) * | 1979-05-29 | 1982-11-16 | Peter J. Schirmann | Activated ester monomers and polymers |
DE3202122A1 (de) * | 1982-01-23 | 1983-07-28 | Röhm GmbH, 6100 Darmstadt | Verfahen zum verfestigen von fasergebilden mittels waessriger kunststoffdispersionen |
US4454301A (en) * | 1982-06-07 | 1984-06-12 | American Cyanamid Company | Crosslinking coating compositions |
-
1985
- 1985-02-28 DE DE19853507154 patent/DE3507154A1/de active Granted
- 1985-12-17 NO NO855106A patent/NO164181C/no not_active IP Right Cessation
-
1986
- 1986-02-11 US US06/830,507 patent/US4689264A/en not_active Expired - Lifetime
- 1986-02-19 DE DE8686102172T patent/DE3684937D1/de not_active Expired - Lifetime
- 1986-02-19 EP EP86102172A patent/EP0193107B1/de not_active Expired - Lifetime
- 1986-02-25 FI FI860802A patent/FI84188C/fi not_active IP Right Cessation
- 1986-02-25 DK DK087686A patent/DK165844C/da not_active IP Right Cessation
- 1986-02-27 JP JP61040518A patent/JPS61201061A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
EP0193107A2 (de) | 1986-09-03 |
DE3507154C2 (enrdf_load_stackoverflow) | 1993-01-21 |
FI860802A0 (fi) | 1986-02-25 |
FI84188C (fi) | 1991-10-25 |
DK87686A (da) | 1986-08-29 |
DK165844B (da) | 1993-01-25 |
DK87686D0 (da) | 1986-02-25 |
NO164181B (no) | 1990-05-28 |
NO855106L (no) | 1986-08-29 |
DE3684937D1 (de) | 1992-05-27 |
JPS61201061A (ja) | 1986-09-05 |
FI860802L (fi) | 1986-08-29 |
US4689264A (en) | 1987-08-25 |
FI84188B (fi) | 1991-07-15 |
NO164181C (no) | 1990-09-05 |
DE3507154A1 (de) | 1986-08-28 |
DK165844C (da) | 1993-06-21 |
EP0193107A3 (en) | 1989-07-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2749386C2 (enrdf_load_stackoverflow) | ||
EP0311908B1 (de) | Verfahren zur Herstellung von wässrigen (Meth)acrylsäureester-Copolymer-Dispersionen in zwei Stufen und deren Verwendung als Imprägnier-, Überzugs- und Bindemittel für flächige Fasergebilde | |
DE69020815T2 (de) | Antistatische Behandlung von Polyolefinfasern. | |
DE2441781C3 (de) | Verfahren zur Verbesserung der Wasseraufnahme und Saugfähigkeit von Fasermaterialien | |
DE3202093A1 (de) | Acrylkunststoffdispersion | |
EP0019169A1 (de) | Verwendung von wässrigen Dispersionen von amidgruppenhaltigen Emulsions-Copolymerisaten zum Verfestigen von Faservliesen | |
EP0084810B1 (de) | Verfahren zum Verfestigen von Fasergebilden mittels wässriger Kunststoffdispersionen | |
DE2117999A1 (enrdf_load_stackoverflow) | ||
DE1645227A1 (de) | Verfahren zur Herstellung von kautschukelastischen Blockmischpolymerisaten,insbesondere von solchen auf Acrylharzbasis | |
DE3902067A1 (de) | Filmbildende, selbstvernetzende waessrige kunststoffdispersion | |
DE2052926B2 (de) | Verwendung eines ternären Äthylen/ Vinylchlorid-Mischpolymerisats als Bindemittel von nicht-gewebtem Fasermaterial | |
EP0047962B1 (de) | Verfahren zur Herstellung von quellfähigen Fäden, Fasern und geformten Gebilden aus Acrylpolymeren sowie die dabei erhaltenen Produkte | |
EP0193107B1 (de) | Gebundenes textiles Flächengebilde und Verfahren zu seiner Herstellung | |
DE2357068C2 (de) | Verfahren zur Herstellung reinigungsbeständiger Vliesstoffe | |
EP0492378B2 (de) | Wässrige Kunststoffdispersionen mit vermindertem Formaldehydgehalt | |
DE2736787A1 (de) | Gegenstand und verfahren zum weichmachen von textilien | |
DE1635684A1 (de) | Verfahren zur Herstellung textiler Flaechengebilde mit filzartigem Charakter | |
DE1277191C2 (de) | Verfahren zur herstellung von gebundenen faservliesen | |
DE2135459C2 (de) | Wässerige Polymerisatdispersion und ihre Verwendung | |
DE1232103B (de) | Verfahren zur Herstellung von Beschichtungen, Impraegnierungen und Verklebungen von Faser-substraten wie Geweben, Vliessen sowie zum Kaschieren von Schaumstoffen mit Geweben unter Verwendung von Pfropfpolymerisaten | |
EP0672073B1 (de) | Verfahren zur herstellung eines siegelbaren, selbstvernetzenden bindemittels | |
DE3911942A1 (de) | Waessrige kunstharzdispersionen | |
DE1444030A1 (de) | Schwer entflammbare,gebundene Faservliese | |
DE69409115T2 (de) | Neues faserfüllmaterial für matte | |
EP0392350B1 (de) | Wässrige Kunstharzdispersionen |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): DE FR NL SE |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): DE FR NL SE |
|
17P | Request for examination filed |
Effective date: 19890803 |
|
17Q | First examination report despatched |
Effective date: 19901204 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE FR NL SE |
|
REF | Corresponds to: |
Ref document number: 3684937 Country of ref document: DE Date of ref document: 19920527 |
|
ET | Fr: translation filed | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
EAL | Se: european patent in force in sweden |
Ref document number: 86102172.3 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20010219 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20010220 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20010228 Year of fee payment: 16 |
|
NLT1 | Nl: modifications of names registered in virtue of documents presented to the patent office pursuant to art. 16 a, paragraph 1 |
Owner name: ROEHM GMBH & CO. KG |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: CJ |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20020214 Year of fee payment: 17 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020901 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020903 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20021031 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee |
Effective date: 20020901 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030220 |
|
EUG | Se: european patent has lapsed |