EP0054573A1 - Procédé de consolidation de produits fibreux à l'aide de dispersions de résine synthétique - Google Patents
Procédé de consolidation de produits fibreux à l'aide de dispersions de résine synthétique Download PDFInfo
- Publication number
- EP0054573A1 EP0054573A1 EP80108012A EP80108012A EP0054573A1 EP 0054573 A1 EP0054573 A1 EP 0054573A1 EP 80108012 A EP80108012 A EP 80108012A EP 80108012 A EP80108012 A EP 80108012A EP 0054573 A1 EP0054573 A1 EP 0054573A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- plastic
- weight
- dispersion
- methacrylic acid
- acrylic
- 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.)
- Granted
Links
- 239000006185 dispersion Substances 0.000 title claims abstract description 58
- 238000000034 method Methods 0.000 title claims abstract description 26
- 238000007596 consolidation process Methods 0.000 title claims description 5
- 239000002657 fibrous material Substances 0.000 title description 2
- 229920003002 synthetic resin Polymers 0.000 title 1
- 239000000057 synthetic resin Substances 0.000 title 1
- 239000004033 plastic Substances 0.000 claims abstract description 46
- 229920003023 plastic Polymers 0.000 claims abstract description 46
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 22
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 19
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000000178 monomer Substances 0.000 claims abstract description 13
- 238000001035 drying Methods 0.000 claims abstract description 9
- 150000003863 ammonium salts Chemical class 0.000 claims abstract description 5
- 239000000126 substance Substances 0.000 claims abstract description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 4
- 125000005907 alkyl ester group Chemical group 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 3
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 claims abstract description 3
- 239000000835 fiber Substances 0.000 claims description 27
- 238000000576 coating method Methods 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 4
- 239000004745 nonwoven fabric Substances 0.000 claims description 4
- 150000003839 salts Chemical group 0.000 claims description 4
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims description 2
- 239000002759 woven fabric Substances 0.000 claims description 2
- 239000004753 textile Substances 0.000 claims 1
- 239000000839 emulsion Substances 0.000 abstract description 6
- 239000008346 aqueous phase Substances 0.000 abstract description 4
- 239000000203 mixture Substances 0.000 abstract description 3
- -1 alkali metal salts Chemical class 0.000 abstract description 2
- 238000005728 strengthening Methods 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 description 19
- 238000006116 polymerization reaction Methods 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000005470 impregnation Methods 0.000 description 8
- 239000004744 fabric Substances 0.000 description 6
- 238000007792 addition Methods 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 4
- 150000007942 carboxylates Chemical group 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- LLLCSBYSPJHDJX-UHFFFAOYSA-M potassium;2-methylprop-2-enoate Chemical compound [K+].CC(=C)C([O-])=O LLLCSBYSPJHDJX-UHFFFAOYSA-M 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 230000008961 swelling Effects 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
- 229920000742 Cotton Polymers 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 235000019395 ammonium persulphate Nutrition 0.000 description 1
- 239000012874 anionic emulsifier Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 239000002557 mineral fiber Substances 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000019394 potassium persulphate Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 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
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920003170 water-soluble synthetic polymer Polymers 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 230000004580 weight loss Effects 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
- D04H1/58—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
- D04H1/587—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 characterised by the bonding agents used
-
- 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
Definitions
- the invention relates to a method for solidifying fiber structures by treatment with aqueous plastic dispersions.
- the choice of the plastic dispersions to be used depends, among other things, on whether the finished fiber structure should be resistant to organic solvents. If this is not the case, plastic dispersions can be used which are free of formaldehyde-releasing substances and whose plastic content is essentially composed, for example, of alkyl esters of acrylic or methacrylic acid, vinyl esters and / or styrene and small amounts of ⁇ , ⁇ -unsaturated carboxylic acids. If, on the other hand, resistance to organic solvents or plasticizers is required, plastic dispersions are used that can be crosslinked at elevated temperatures after coating or soaking and drying.
- crosslinking is achieved either by adding water-soluble aminoplast resins to the dispersions of the type mentioned above or by using plastic dispersions in the formation of which condensable formaldehyde derivatives, in particular N-methylol-aorylamide or -methacrylamide, are involved.
- the invention has for its object to provide fiber structures with an equipment which is at least limited solvent-resistant or block-free or tack-free, and for this purpose to use an aqueous plastic dispersion which is free of formaldehyde-releasing substances and whose plastic content consists predominantly of alkyl esters of acrylic or methacrylic acid, and small amounts of ⁇ , ß-tm saturated carboxylic acids.
- Stability of the coatings or impregnations produced according to the invention depends on the fact that the acrylic or methacrylic acid in the form of its alkali metal or ammonium salt is dissolved in the template in the preparation of the plastic dispersion to be used by the feed process.
- Equivalent plastic dispersions cannot be prepared by gradually adding the acrylic or methacrylic acid or its salts together with the other monomers during the feed process, or by adding the acrylic or methacrylic acid as such to the initial charge and only neutralizing it after the polymerization.
- plastic dispersions which are free of formaldehyde-releasing substances by the process indicated above are known from OE-PS 236 643 and from FR-PS 1 157 265.
- the plastic dispersions produced in this way have not yet been used to solidify fiber structures.
- the impregnations and coatings obtained in this way would be distinguished by improved resistance to organic solvents.
- Plastic dispersions with a minimum film-forming temperature are particularly advantageous for the process of the invention below 25 ° C and with a T ⁇ max value of the dispersed plastic (according to DIN 53445) below 50 ° C.
- the plastic portion of the dispersion is preferably composed of more than 50% by weight of acrylic acid alkyl esters with 1 to 8 carbon atoms in the alkyl radical and the rest predominantly of methacrylic acid alkyl esters with 1 to 4 carbon atoms in the alkyl radical.
- Other water-insoluble monomers, such as styrene, vinyl acetate or vinylidene chloride can be involved in minor amounts in the construction of the plastic.
- the proportion of acrylic and / or methacrylic acid polymerized in salt form is preferably 2 to 3% by weight, calculated as free acid and. based on the weight of the plastic.
- the alkali salts are preferably the sodium and potassium salts.
- the ammonium salts can be derived from ammonia or from organic amines, such as, for example, ethanolamine.
- the preferred method for producing the plastic dispersion is the emulsion feed method. Part of the amount of water provided as the aqueous phase of the dispersion is placed in the polymerization vessel and the salt of acrylic and / or methacrylic acid is dissolved therein.
- a conventional anionic or nonionic emulsifier and a water-soluble polymerization initiator, such as potassium or ammonium peroxydisulfate, can be dissolved in the initial charge.
- the initial charge is brought to a temperature suitable for carrying out the polymerization, preferably to about 50 to 80 ° C.
- the monomers to be polymerized are emulsified, for which purpose a further amount of an emulsifier is advantageously used.
- the monomer emulsion is gradually let into the Run in template while the polymerization is taking place at the same time.
- Additional polymerization initiators can be added continuously or in individual additions during the polymerization.
- the amount of water and monomers are preferably matched to one another in such a way that a 40-60% dispersion is formed.
- the use of emulsifiers can optionally be dispensed with.
- the monomers, besides the acrylic acid or methacrylic acid salt, can also be added gradually in non-emulsified form. In this case, the entire water phase is added to the template at the beginning of the process.
- the fiber structures that are consolidated according to the invention can consist of natural fibers, man-made fibers or of mixtures of different types of fibers.
- the consolidation of mineral fiber structures e.g. made of glass fibers or rock wool.
- Flat fiber structures are essentially equipped; these include woven fabrics, knitted fabrics, non-woven fabrics, and papers, in particular absorbent base papers and cardboards.
- the plastic dispersion can be applied as a coating on the surface of the fiber structure.
- the fiber structure is preferably treated with the plastic dispersion in such a way that an impregnation which strengthens the entire cross section is achieved.
- Plastic dispersion depends on the intended use of the solidified fiber structure. It can range from a slight consolidation with 5 - 20% dry plastic weight, based on the fiber weight, to a plastic filling with 100% by weight plastic, based on the fiber weight, or more.
- a preferred application of the invention is the consolidation of light nonwovens with a weight per unit area of not more than 60 g / m2.
- the dispersion can be applied to or introduced into the fiber structure by impregnation, spraying, splashing, brushing or printing. Depending on the application method used, the dispersion can be applied as a dilute liquor, for example with a binder content of 15 to 30% by weight, or as a thickened paste or as a foam. Conventional thickeners, such as cellulose derivatives or water-soluble synthetic polymers, can be reacted in the pastes; the binder content is preferably 20 to 40% by weight.
- the coated or impregnated fiber structure is dried. Conventional flat web dryers, cylinder dryers or screen drum dryers can be used for this.
- the treated fiber structure is less prone to sticking to warm metal surfaces than products equipped with purely thermoplastic dispersions.
- the so-called "binder tri wash loss”, abbreviated BTV, is suitable, the determination of which is explained in more detail in the examples under IV.
- BTV binder tri wash loss
- the binder loss in the fiber structures impregnated by the process of the invention is reduced to a fraction of this value.
- an alkali methacrylate content of 1% (calculated as methacrylic acid, based on the plastic weight), a BTV value between 30 and 50% is achieved.
- BKV Binder-Kochwasch-loss
- the BKV value depends to a large extent on the drying temperature. After drying at room temperature, BKV values of up to 70% are observed. After drying or reheating at temperatures between 80 and 120 ° - especially with a low carboxylate content - only binder losses of a few percent can be determined.
- binder losses In the preferred range of 2-3% by weight of carboxylate units, binder losses of between 4 and 10% by weight occur.
- the binder losses depend on the type of fiber material and the plastic dispersion; the values mentioned here apply to a polyester fabric which was equipped with 50% by weight of a plastic dispersion composed of methyl methacrylate and butyl acrylate as the main components.
- Comparative dispersion C prepared in accordance with Example 10, but with the addition of methacrylic acid in the form of the free acid together with the monomer feed.
- Comparative dispersion D prepared like comparative dispersion C, but neutralized the methacrylic acid units with the equivalent amount of KOH after completion of the polymerization.
- Comparative dispersion E prepared as in Example 10, but gradual addition of the potassium methacrylate simultaneously with the addition of the other monomers.
- a polyester fabric with a basis weight of 100 g / m 2 made of polyester staple fibers is soaked with a dispersion at room temperature and by means of a laboratory pad squeezed to a liquor absorption of 80 to 100% (based on the weight of the fabric).
- the moist fabric strip is dried in a tensioned state for 5 minutes at 120 ° C in a forced-air drying cabinet.
- Tri ⁇ sche A sample of 18 x 18 cm size is 80 * moves min at 20 C with 125 ml trichlorethylene, then rinsed with 100 ml trichlorethylene and dried for 30 min at 80th After storage for half an hour at room temperature, the sample is weighed out. The weight loss is determined in percent, based on the weight of the binder in the sample used.
- Cottons A sample of 18 x 18 cm in size is washed for 10 min at 90 ° with 125 ml of an aqueous washing liquor containing 3 g of Marseille soap and 2 g of calc. Soda contains, agitated, then rinsed once with 90 ° C hot and once with cold water and Dried at 90 ° C for 30 min. 30 minutes after drying, the sample is weighed and the binder loss in percent, based on the weight of the binder in the sample used, is determined.
- the comparative dispersions show that without neutralization of the carboxyl groups of the binder polymer (comparative dispersion C) very high binder losses occur during tri-washing. These losses are significantly reduced by neutralization, while the losses in hot water only increase insignificantly despite the increased polarity of the binder. With subsequent neutralization (comparative dispersion D), particularly low binder losses are found, but the tests described under III indicate a high sensitivity of the film to plasticizers. If the methacrylic acid salt (reference dispersion E) is added uniformly, the binder losses are higher than when used in the receiver according to the invention (example 10), but significantly lower than in the case of non-neutralized binder resin. In contrast, the swelling in the plasticizer (see under III) is unfavorably high.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Reinforced Plastic Materials (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP80108012A EP0054573B1 (fr) | 1980-12-18 | 1980-12-18 | Procédé de consolidation de produits fibreux à l'aide de dispersions de résine synthétique |
| DE8080108012T DE3070134D1 (en) | 1980-12-18 | 1980-12-18 | Process for the consolidation of fibrous material with dispersions of synthetic resin |
| AT80108012T ATE11681T1 (de) | 1980-12-18 | 1980-12-18 | Verfahren zum verfestigen von fasergebilden mit kunststoffdispersionen. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP80108012A EP0054573B1 (fr) | 1980-12-18 | 1980-12-18 | Procédé de consolidation de produits fibreux à l'aide de dispersions de résine synthétique |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0054573A1 true EP0054573A1 (fr) | 1982-06-30 |
| EP0054573B1 EP0054573B1 (fr) | 1985-02-06 |
Family
ID=8186934
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP80108012A Expired EP0054573B1 (fr) | 1980-12-18 | 1980-12-18 | Procédé de consolidation de produits fibreux à l'aide de dispersions de résine synthétique |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0054573B1 (fr) |
| AT (1) | ATE11681T1 (fr) |
| DE (1) | DE3070134D1 (fr) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0012033A1 (fr) * | 1978-12-04 | 1980-06-11 | Rohm And Haas Company | Articles non-tissés et leur préparation |
-
1980
- 1980-12-18 DE DE8080108012T patent/DE3070134D1/de not_active Expired
- 1980-12-18 AT AT80108012T patent/ATE11681T1/de active
- 1980-12-18 EP EP80108012A patent/EP0054573B1/fr not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0012033A1 (fr) * | 1978-12-04 | 1980-06-11 | Rohm And Haas Company | Articles non-tissés et leur préparation |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0054573B1 (fr) | 1985-02-06 |
| DE3070134D1 (en) | 1985-03-21 |
| ATE11681T1 (de) | 1985-02-15 |
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