EP0151170A1 - Toile a bache de protection et son procede de fabrication. - Google Patents
Toile a bache de protection et son procede de fabrication.Info
- Publication number
- EP0151170A1 EP0151170A1 EP84902919A EP84902919A EP0151170A1 EP 0151170 A1 EP0151170 A1 EP 0151170A1 EP 84902919 A EP84902919 A EP 84902919A EP 84902919 A EP84902919 A EP 84902919A EP 0151170 A1 EP0151170 A1 EP 0151170A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fabric
- polyacrylic acid
- base fabric
- protective tarpaulin
- acid ester
- 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
- 239000004744 fabric Substances 0.000 title claims abstract description 53
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- 150000002148 esters Chemical class 0.000 claims abstract description 28
- 229920002125 Sokalan® Polymers 0.000 claims abstract description 27
- 239000004584 polyacrylic acid Substances 0.000 claims abstract description 27
- 239000000049 pigment Substances 0.000 claims abstract description 20
- 229920000728 polyester Polymers 0.000 claims abstract description 19
- 230000001681 protective effect Effects 0.000 claims abstract description 19
- 229920002635 polyurethane Polymers 0.000 claims abstract description 15
- 238000000576 coating method Methods 0.000 claims abstract description 14
- 239000004814 polyurethane Substances 0.000 claims abstract description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 8
- 239000006185 dispersion Substances 0.000 claims abstract description 8
- 229910000906 Bronze Inorganic materials 0.000 claims abstract description 6
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 6
- 239000010974 bronze Substances 0.000 claims abstract description 6
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000001035 drying Methods 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 239000011343 solid material Substances 0.000 abstract 2
- 239000002671 adjuvant Substances 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 229920003180 amino resin Polymers 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- SYDYRFPJJJPJFE-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(N(CO)CO)=NC(N(CO)CO)=N1 SYDYRFPJJJPJFE-UHFFFAOYSA-N 0.000 description 2
- 125000005396 acrylic acid ester group Chemical group 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 125000005395 methacrylic acid group Chemical group 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- -1 siloxanes Chemical class 0.000 description 2
- 239000000080 wetting agent Substances 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 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- MNPKKYZUEZVQNJ-UHFFFAOYSA-N 2-methylprop-2-enyl carbamate Chemical compound CC(=C)COC(N)=O MNPKKYZUEZVQNJ-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-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
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 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
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- MGPYDQFQAJEDIG-UHFFFAOYSA-N ethene;urea Chemical class C=C.NC(N)=O MGPYDQFQAJEDIG-UHFFFAOYSA-N 0.000 description 1
- YGZXCVSWQWFWAA-UHFFFAOYSA-N ethenyl acetate;propanoic acid Chemical compound CCC(O)=O.CC(=O)OC=C YGZXCVSWQWFWAA-UHFFFAOYSA-N 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920003009 polyurethane dispersion Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/18—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with two layers of different macromolecular materials
- D06N3/183—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with two layers of different macromolecular materials the layers are one next to the other
Definitions
- the invention relates to a waterproof, heat-reflecting tarpaulin and a method for its production.
- the waterproofing of heavy fabrics is carried out in a customary manner in two or more bath processes, a water-insoluble metal soap being produced on the goods and the fabric pores additionally being closed by fillers and paraffin or the like (see W. Bernard, "Appretur der Textilien", 2nd edition 1967, Springer-Verlag, pages 326 ff).
- absolutely waterproof fabrics can be obtained by coating, where as coating agent i.a. Polyvinyl chloride is used.
- the object of the invention is therefore to provide waterproof, heat-reflecting tarpaulin fabrics which are distinguished by a low overall weight.
- this object is achieved in that a polyester lightweight fabric of at most 160 g / m 2 is provided on one side with at least one pigment-containing layer of a crosslinked polyacrylic acid ester and a cover layer made of polyurethane, preferably aliphatic polyurethane, the coatings totaling 25 to 80 make up g / m 2 .
- the process according to the invention for the production of waterproof, heat-reflecting protective tarpaulin fabrics is characterized in that at least one line (corresponding to one layer) by means of an aqueous, pigment-containing, cross-linkable material on an optionally pretreated polyester lightweight fabric of maxiral 160 g / m 2 as base fabric
- Polyacrylic acid ester dispersion and a top coat using a polyurethane, preferably aliphatic polyurethane are applied with the use of customary auxiliaries, with intermediate drying, with only enough solid being applied during the individual coats that the finished tarpaulin material contains 25 to 80 g / m 2 solid coatings on the base fabric.
- Polyester lightweight fabric has proven to be particularly suitable as the base fabric for the protective tarpaulin fabrics according to the invention, although the same can also be reinforced by small amounts of araid threads.
- Lightweight fabrics are to be understood to mean those whose square meter weight is between 80 and 160 g, in particular between 90 and 120 g.
- Protective tarpaulin fabrics with a particularly smooth surface are obtained if a light polyester filament fabric is used as the base fabric, which is why this type of fabric is particularly preferred.
- the crosslinkable polyacrylic acid esters that can be used are known from the prior art.
- the crosslinkable polyacrylic acid esters contain as reactive groups e.g. N-methylol groups, especially carboxamide methylol groups.
- Etherified N-methylol groups where alcohols containing one to three carbon atoms, in particular methanol, have been used for the etherification, are also suitable as crosslinkable groups.
- the monomers which carry these crosslinkable groups are generally known. N-addition products of formaldehyde with methacrylamide or acrylamide and allyl or methallyl carbamate may be mentioned.
- crosslinkable polyacrylic acid esters can also be used as reactive groups e.g. Contain glycidyl residues. These comonomers are also well known. An example is allyglycidyl ether.
- crosslinkable polyacrylic acid esters are also - and this group of copolymers is preferred - also to be understood as meaning those which contain reactive comonomers which have a suitable curing or crosslinking agent, e.g. need conventional aminoplast resins or silanes and / or siloxanes containing amino groups.
- suitable curing or crosslinking agent e.g. need conventional aminoplast resins or silanes and / or siloxanes containing amino groups.
- examples of such comonomers are those which have free OH groups, e.g. 2-hydroxyethyl and 3-hydroxypropyl acrylate or methacrylate.
- Unsaturated carboxylic acids, e.g. Acrylic acid and methacrylic acid and their amides lead to crosslinked polyacrylic acid esters with aminoplast resins. The latter are very preferably polymerized in, since these protective tarpaulin materials with these coatings are characterized by a particularly good overall result.
- the copolymers used can also contain several of the comonomers mentioned.
- the amounts of comonomers with crosslinkable groups are about 1.0 to 15, in particular 2 to 10,% by weight, based on the total copolymer.
- the monomers also contained in the polyacrylic acid esters are also known.
- methacrylic or acrylic acid esters for example methacrylic or acrylic acid esters of alcohols having one to eight carbon atoms, such as methanol, ethanol, butanol, isobutanol or 2-ethylhexanol, which are generally in amounts of 45-99.0% by weight.
- comonomers for example vinyl acetate, ethylene, styrene, vinyl chloride and particularly preferably acrylonitrile, are also copolymerized in the polymers used. These comonomers are present in amounts of up to 40% by weight, based on the total polymer.
- crosslinkable polyacrylic acid esters described come in the form of about 30-70% by weight. % dispersions in the trade.
- Pigments are incorporated into the crosslinkable polyacrylic acid ester dispersions. mixed in, which favor the heat reflection.
- Metal powders are particularly suitable as such pigments. Examples of metals that can be mentioned are aluminum, nickel, silver, zinc and alloys such as brass, bronze, aluminum-bronze and the like. Aluminum and aluminum-bronze are preferred for economic reasons.
- other heat-reflecting pigments such as polyester flicker or mica, are also very suitable.
- the amount of pigment can vary within wide limits. Already 5% by weight, based on cross-linked polyacrylic acid esters, has a clear effect. It preferably contains 8-30% by weight, particularly preferably 10-25% by weight, based on crosslinked polyacrylic acid esters.
- the upper limit is determined by economic considerations, but also by decreasing adhesion and fastness to rubbing of the polymer film, and is approximately 60% by weight, based on crosslinked polyacrylic acid esters. If two or more coats of crosslinkable polyacrylic acid ester are used, it has proven useful to mix only a small amount of pigment, about a quarter to a third of the total amount of pigment, with the first coat and the majority of pigment into the second and add another line, as this significantly improves the film's adhesion. However, it is also possible to do without the pigment addition in the first stroke, but this method of working is less suitable.
- the polyurethanes used for the top coat also belong to the prior art. It is therefore not necessary to go into these connections in more detail.
- the aliphatic polyurethanes are particularly suitable because they have improved light fastness.
- the top coat can be done either from an aqueous or organic medium.
- the raw polyester lightweight fabrics are washed in a known manner and then optionally pretreated as usual. Pretreatment improves film adhesion somewhat.
- the coating itself is also carried out in a known manner.
- the light polyester base fabric is coated on one side with at least one coat of the pigment-containing polyacrylic acid ester and dried in between. It is particularly preferred to work with two layers of polyacrylic acid ester, the small amounts required being applied preferably by means of an air knife.
- the polyurethane is then applied as a top coat, also preferably with an air knife (for further details, see examples).
- the usual auxiliaries such as crosslinking agents, thickeners, pH regulators, etc. are also used in the application.
- the simultaneous use of conventional aminoplast resins, water repellents, color pigments and the like is also readily possible and is also expedient and advantageous from case to case.
- the amounts of such additives are known to the person skilled in the art.
- a protective tarpaulin material is obtained which is distinguished from the known products by remarkable, surprising advantages. Because of the state of the art it was not to be expected that such a light yet mechanically strong protective tarpaulin material would be possible to deliver.
- the special base fabric used and the addition of the heat-reflecting pigments to the crosslinkable polyacrylic acid esters make it possible to manufacture the advantageous tarpaulin fabrics in a simple manner. This is not only characterized by its high strength and low weight, but also leaves nothing to be desired in terms of water resistance and heat reflection.
- the articles made from it, especially tarpaulins allow easy handling and are therefore easy to use.
- a polyester filament fabric (110 g / m 2 ) is prewashed in the customary manner (2 g / 1 anionic wetting agent, 2 g / 1 calcined soda and 3 g / 1 phosphate complexing agent), rinsed at 90 ° C. for 20 minutes and dried and 60 seconds at 190 ° C heat set.
- the fabric is then pre-fouled with the following aqueous liquor
- the coating is carried out in three layers by means of an air knife, a total solid coating of 40 g / m 2 being obtained.
- the following paste is used for the first stroke, applied with a squeegee:
- the pH should not be above 7.
- the second coat is also applied with a squeegee using the same paste, but containing 100 pbw of aluminum powder.
- the protective tarpaulin has a very considerable heat reflection.
- Example 1 is repeated, but using polyester flicker instead of aluminum powder.
- polyester filament fabric described there in Example 1 is washed and pretreated in the manner described there.
- the coating is also carried out in the manner described in Example 1, but the following coating pastes and a total coating of 60 g / m 2 are used:
- the top coat is produced in accordance with EP-A-41 607, Example 1.
- a light polyester fabric (130 g / m 2 ) is finished in the manner described in Example 2 (total solid layer 50 g / m 2 )
- the technological properties of the tarpaulin fabric correspond to the values obtained there.
- Example 1 is repeated, but only 2 lines are applied, in accordance with the 2nd line (now 1st line) described in Example 1 and the top line described in Example 1.
- the total application quantity is 45 g / m 2 .
- the tarpaulin fabric obtained is technologically sound.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Laminated Bodies (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT84902919T ATE22943T1 (de) | 1983-07-27 | 1984-07-19 | Schutzplanenstoff und verfahren zu dessen herstellung. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3327016 | 1983-07-27 | ||
DE3327016A DE3327016C2 (de) | 1983-07-27 | 1983-07-27 | Schutzplanenstoff und Verfahren zu dessen Herstellung |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0151170A1 true EP0151170A1 (fr) | 1985-08-14 |
EP0151170B1 EP0151170B1 (fr) | 1986-10-15 |
Family
ID=6205015
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP84902919A Expired EP0151170B1 (fr) | 1983-07-27 | 1984-07-19 | Toile a bache de protection et son procede de fabrication |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0151170B1 (fr) |
DE (2) | DE3327016C2 (fr) |
WO (1) | WO1985000626A1 (fr) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU4578099A (en) * | 1998-06-17 | 2000-01-05 | Milliken & Company | Polyurethane/polyacrylate dispersion coating for airbag fabrics |
DE102004016773B3 (de) * | 2004-04-01 | 2005-11-17 | Sattler Ag | Beschichtungsmittel für Sonnenschutzartikel |
WO2016178057A1 (fr) * | 2015-05-04 | 2016-11-10 | Pratrivero S.P.A. | Procédé de fabrication d'un tissu multicouche ignifuge et/ou étanche à l'eau, et tissu multicouche ignifuge et/ou étanche à l'eau |
CN105088807A (zh) * | 2015-09-22 | 2015-11-25 | 浙江新达经编有限公司 | 一种防老化高强度复合面料及其制备方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1226072B (de) * | 1957-05-18 | 1966-10-06 | Roehm & Haas Gmbh | Verfahren zum Beschichten textiler Gebilde |
FR1394801A (fr) * | 1964-01-28 | 1965-04-09 | Cellophane Sa | Procédé de fabrication d'un tissu enduit pour vêtements |
DE1247259B (de) * | 1964-05-19 | 1967-08-17 | Bayer Ag | Verfahren zur Erzeugung von loesungsmittelbestaendigen Textilbeschichtungen |
DE2013265A1 (en) * | 1970-03-20 | 1971-10-14 | Dr. Th. Böhme KG, Chem. Fabrik, 8192 Gartenberg | Solvent resistant grained leather prepn |
GB1353609A (en) * | 1970-06-09 | 1974-05-22 | Nairn Williamson Ltd | Production of coated fabrics |
CH539729A (it) * | 1970-07-01 | 1973-07-31 | Sir Soc Italiana Resine Spa | Procedimento per la fabbricazione di materiali poromerici |
-
1983
- 1983-07-27 DE DE3327016A patent/DE3327016C2/de not_active Expired
-
1984
- 1984-07-19 DE DE8484902919T patent/DE3460990D1/de not_active Expired
- 1984-07-19 EP EP84902919A patent/EP0151170B1/fr not_active Expired
- 1984-07-19 WO PCT/EP1984/000224 patent/WO1985000626A1/fr active IP Right Grant
Non-Patent Citations (1)
Title |
---|
See references of WO8500626A1 * |
Also Published As
Publication number | Publication date |
---|---|
DE3460990D1 (en) | 1986-11-20 |
DE3327016A1 (de) | 1985-02-14 |
WO1985000626A1 (fr) | 1985-02-14 |
EP0151170B1 (fr) | 1986-10-15 |
DE3327016C2 (de) | 1986-09-25 |
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