EP0837176B1 - Tack-rag - Google Patents
Tack-rag Download PDFInfo
- Publication number
- EP0837176B1 EP0837176B1 EP96116910A EP96116910A EP0837176B1 EP 0837176 B1 EP0837176 B1 EP 0837176B1 EP 96116910 A EP96116910 A EP 96116910A EP 96116910 A EP96116910 A EP 96116910A EP 0837176 B1 EP0837176 B1 EP 0837176B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- tack
- water
- resin
- groups
- rag
- 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
- 229920005989 resin Polymers 0.000 claims abstract description 81
- 239000011347 resin Substances 0.000 claims abstract description 81
- 239000004744 fabric Substances 0.000 claims abstract description 38
- 239000000463 material Substances 0.000 claims abstract description 37
- 238000001035 drying Methods 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000004094 surface-active agent Substances 0.000 claims abstract description 8
- 125000003010 ionic group Chemical group 0.000 claims description 22
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 230000003472 neutralizing effect Effects 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 14
- 238000006386 neutralization reaction Methods 0.000 claims description 13
- 238000004140 cleaning Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 125000000129 anionic group Chemical group 0.000 claims description 5
- 125000002091 cationic group Chemical group 0.000 claims description 5
- 238000005406 washing Methods 0.000 abstract description 4
- 239000002699 waste material Substances 0.000 abstract description 4
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 10
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- -1 polypropylene Polymers 0.000 description 6
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 229920000297 Rayon Polymers 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 4
- 238000007598 dipping method Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 2
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- CDBAMNGURPMUTG-UHFFFAOYSA-N 4-[2-(4-hydroxycyclohexyl)propan-2-yl]cyclohexan-1-ol Chemical compound C1CC(O)CCC1C(C)(C)C1CCC(O)CC1 CDBAMNGURPMUTG-UHFFFAOYSA-N 0.000 description 1
- 241000282979 Alces alces Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000006701 autoxidation reaction Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 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
- 239000000356 contaminant Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 239000002649 leather substitute Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229940117969 neopentyl glycol Drugs 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/61—Polyamines polyimines
-
- A—HUMAN NECESSITIES
- A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
- A47L—DOMESTIC WASHING OR CLEANING; SUCTION CLEANERS IN GENERAL
- A47L25/00—Domestic cleaning devices not provided for in other groups of this subclass
- A47L25/005—Domestic cleaning devices not provided for in other groups of this subclass using adhesive or tacky surfaces to remove dirt, e.g. lint removers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/327—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
- D06M15/333—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/507—Polyesters
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/53—Polyethers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/55—Epoxy resins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
- D06M15/568—Reaction products of isocyanates with polyethers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
- D06M15/572—Reaction products of isocyanates with polyesters or polyesteramides
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
Definitions
- the present invention relates generally to tacky cloths suitable for the removal of dirt, dust and other particulate contaminants (hereinafter simply referred to as dirt) from various surfaces.
- tacky cloths are commonly referred to as tack-rags.
- Tack-rags are normally produced by dipping a cloth material in a solution or dispersion of a tacky resin, then allowing the liquid medium to evaporate.
- the resins generally utilized are water-insoluble in order to facilitate cleaning and further use. Eventually, however, the tack-rags wear out and must be thrown away.
- a tack-rag which comprises a cloth material impregnated with a tacky resin, characterized in that the tacky resin is a non-drying tacky resin comprising an oligomer or polymer which possesses
- the tack-rags in accordance with the present invention have the advantage that, subsequent to use, they can be water-washed to substantially completely separate the resin and collected dirt from the cloth material.
- the resin is water-soluble because it possesses a water-solubilizing amount of (a) one or more non-ionic water-solubilizing groups, (b1) one or more ionic groups which have been neutralized with a non-volatile neutralizing agent in order to render those ionic groups water-solubilizing or (c) combinations thereof, it is not necessary to utilize any additives such as tensides in the wash water to effect substantially complete separation of the resin from the cloth material.
- the only needed additive to the wash water is a non-volatile neutralizing agent which becomes associated with the ionic groups of the resin in order to render the ionic groups water-solubilizing and the resin water-soluble. Again, therefore, no tensides and the like are needed to effect substantially complete separation of the resin from the cloth material.
- the so-washed cloth material if in sufficiently good shape, can be reimpregnated with the tacky resin and used again as a tack-rag, or can merely be used for normal cleaning purposes. If disposal of the cloth material is required, the cloth material being substantially free of resin can simply be disposed of as normal waste.
- the resin dissolved in the wash water can readily be recycled by removal of the dirt, e.g., by filtration, then concentration of the resin solution.
- the concentrated resin solution can then be reused as such or combined with fresh resin solution for (re)impregnating the cloth material.
- the tack-rags in accordance with the present invention comprise a cloth material impregnated with a tacky resin, characterized in that the tacky resin is a non-drying tacky resin comprising an oligomer or polymer which possesses
- cloth materials Any one of a number of natural and/or artificial cloth materials may be considered suitable for use with the present invention.
- These cloth materials are generally known to those skilled in the art and include, for example, woven, non-woven and knitted cloths of cotton, polyester, wool, acrylic, nylon, rayon, cellulose (papers) and viscose fibers, as well as natural and synthetic leather.
- woven, non-woven and knitted cloths of cotton, polyester, wool, acrylic, nylon, rayon, cellulose (papers) and viscose fibers as well as natural and synthetic leather.
- cotton, staple rayon and mixtures thereof are especially preferred.
- tacky resins may be mentioned those that are non-drying and either water-soluble or capable of being rendered water-soluble by neutralizing ionic groups with a non-volatile neutralizing agent.
- non-drying it is meant that the resin dries by physical evaporation of the solvents to form a film in which the resin molecules retain their original chemical form, i.e., essentially no chemical reaction occurs such as crosslinking with a curing agent or via autoxidation at temperatures of up to about 150°C.
- the resin therefore, should retain its tacky character at temperatures of normal use.
- Suitable non-ionic water-solubilizing groups are well-known to those skilled in the art and include, for example, polyoxyalkylene groups such as polyoxyethylene and polyoxypropylene groups, as well as other hydrophilic groups based upon polyvinyl alcohols, polymers of hydroxy (meth)acrylates and other hydroxyl groups-containing oligomers and polymers. Preferred among these for use with the present invention are the polyoxyalkylene groups and, especially, polyoxyethylene groups.
- Suitable ionic groups which require neutralization in order to be water-solubilizing are once again well-known to those skilled in the art and include, for example, carboxyl (anionic) and amino (cationic) groups, which are preferred.
- these ionic groups must be capable of being rendered water-solubilizing by neutralization with a non-volatile neutralizing agent.
- non-volatile is it meant that the neutralizing agent, once associated with the ionic group, does not readily dissociate from it and evaporate on drying. In other words, the salt formed on neutralization remains part of the resin upon drying, which is considered important in order to provide solubility of the resin in the wash water without the necessity for using additional tensides.
- Suitable non-volatile neutralizing agents for anionic groups include strong bases such as alkali metal hydroxides, as well as higher molecular weight polyoxyalkylene amines such as those commercially available under the trade designation "Jeffamine” from Texaco Chemical Company.
- Preferred for use with the present invention include the alkali metal hydroxides such as LiOH, NaOH and KOH.
- Suitable non-volatile neutralizing agents for cationic groups include inorganic strong acids such as phosphoric acid and sulfuric acid, as well as organic acids such as fatty acids and citric acid. Preferred for use with the present invention is phosphoric acid.
- the resin should have an acid number or amine number of at least 20, preferably in the range of 20 to 275, and especially in the range of 40 to 90, in order for the resin to be rendered water-soluble upon neutralization of the ionic groups.
- the resins may also comprise combinations of these various water-solubilizing groups. If such combinations are utilized, one skilled in the art can readily determine the required amount of each of such groups in order to render the resin water-soluble.
- resins suitable for use with the present invention may be mentioned the following:
- the cloth material may be impregnated with the tacky resin in any normal manner such as, for example, by dipping the cloth material into a solution or dispersion of the tacky resin or spraying such solution onto the cloth material, then allowing the solvent to evaporate. Evaporation can be accelerated through drying at slightly elevated temperatures and/or via air convection.
- suitable solvents may be mentioned any one of a number of organic solvents such as, for example, butyl acetate, xylene, white spirits and mixtures of water and a water-miscible solvent such as butyl glycol, as well as water in the case that the tacky resins are water-soluble.
- organic solvents such as, for example, butyl acetate, xylene, white spirits and mixtures of water and a water-miscible solvent such as butyl glycol, as well as water in the case that the tacky resins are water-soluble.
- solutions or dispersions of the resins are utilized for impregnating the cloth material with the tacky resins.
- a dipping procedure is generally used with a continuous roll of material being passed through a bath of resin solution.
- the viscosity of the solution is adjusted such that, after passing through rollers to remove excess resin then drying at ca. 100°C for 5-10 minutes, the weight of the so-impreganted cloth material amounts to 180-220% of the original cloth material weight (80-120% by weight added resin based upon the orignal weight of the cloth material).
- This procedure is controlled by weighing samples of the cloth material before and after impregnation.
- the so-impregnated cloth material is then suitable for use as a dirt collector in various fields, but is especially suited for use as a tack-rag in the automotive field.
- the tack-rags impregnated with a water-soluble non-drying tacky resin as described above can be readily cleaned by washing in water without the addition of tensides or the like which might create disposal problems with respect to the wash water. By so-washing the tack-rags, the resin and dirt can readily be substantially completely separated from the cloth material.
- the tack-rags impregnated with a non-water-soluble non-drying tacky resin as described above can be washed in the same manner as those impregnated with a water-soluble resin with the exception that the wash water must contain a sufficient amount of a non-volatile neutralizing agent in order to neutralize a water-solubilizing amount of ionic groups present in such resin. Again by so-washing, the resin and dirt can readily be substantially completely separated from the cloth material.
- the so-washed cloth material if in sufficiently good shape, can be reimpregnated with the tacky resin and used again as a tack-rag, or can merely be used for normal cleaning purposes. If disposal of the cloth material is required, the cloth material being substantially free of resin and dirt can simply be disposed of as normal waste.
- the resin dissolved in the wash water can readily be recycled by removal of the dirt, e.g, by filtration, then concentration of the resin solution.
- the concentrated resin solution can then be reused as such or combined with fresh resin solution for (re)impregnating the cloth material.
- a non-drying alkyd resin (from unsaturated branched fatty acids, dicarboxylic acids and polyols), having a molecular weight of 1480 and an acid value of 68, was thinned with a 70/30 butyl acetate/butyl glycol solution to a solid content of 60 wt% and subsequently neutralized to 70% with a 40 wt% solution of sodium hydroxide in water.
- An epoxide-amine adduct from one mole of an epoxide resin (commercially available under the trade designation Epikote 828 from Shell) and two moles diethanolamine was thinned with butyl acetate to 60 wt%, then further thinned with butyl acetate to a viscosity of 50 seconds (DIN 4mm cup, 23°C).
- An epoxide-amine adduct from one mole of an epoxide resin (commercially available under the trade designation Epikote 1001 from Shell) and two moles diethanolamine was thinned with butyl acetate to 60 wt% then subsequently neutralized to 100% with phosphoric acid.
- Cotton/rayon mixed cloth material was impregnated by dipping in the resin solution until, after drying at 100°C for 10 minutes, the cloth weighed about 200% of its original weight.
- Tack-rags so-produced from each of Resin Solutions 1-5 had a tacky feel and exhibited excellent tack-rag properties, removing dirt from painted panels completely without smearing or leaving any residue on the painted surface.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Filtering Materials (AREA)
- Filtering Of Dispersed Particles In Gases (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Inorganic Fibers (AREA)
- Laminated Bodies (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK96116910T DK0837176T3 (da) | 1996-10-21 | 1996-10-21 | Støveklud |
| ES96116910T ES2159339T3 (es) | 1996-10-21 | 1996-10-21 | Trapo pegajoso. |
| EP96116910A EP0837176B1 (en) | 1996-10-21 | 1996-10-21 | Tack-rag |
| DE69613982T DE69613982T2 (de) | 1996-10-21 | 1996-10-21 | Staubbindetuch |
| AT96116910T ATE203289T1 (de) | 1996-10-21 | 1996-10-21 | Staubbindetuch |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP96116910A EP0837176B1 (en) | 1996-10-21 | 1996-10-21 | Tack-rag |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0837176A1 EP0837176A1 (en) | 1998-04-22 |
| EP0837176B1 true EP0837176B1 (en) | 2001-07-18 |
Family
ID=8223320
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP96116910A Expired - Lifetime EP0837176B1 (en) | 1996-10-21 | 1996-10-21 | Tack-rag |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0837176B1 (da) |
| AT (1) | ATE203289T1 (da) |
| DE (1) | DE69613982T2 (da) |
| DK (1) | DK0837176T3 (da) |
| ES (1) | ES2159339T3 (da) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001080706A1 (en) * | 2000-04-20 | 2001-11-01 | Milliken & Company | Wiper with particle attracting finish |
| US7048806B2 (en) | 2003-12-16 | 2006-05-23 | The Clorox Company | Cleaning substrates having low soil redeposition |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB610170A (en) * | 1946-03-29 | 1948-10-12 | Bertram Pusey Ridge | Plastic articles reinforced with filaments, fibres, yarns, fabrics and the like |
| US3208093A (en) * | 1960-05-31 | 1965-09-28 | Fred M Greider | Tack cloth coated with plasticized synthetic resin and method for preparing same |
| US3682690A (en) * | 1970-06-17 | 1972-08-08 | Homer C Amos | Article coated with a water-washable tacky elastomer |
| IN141819B (da) * | 1975-04-14 | 1977-04-23 | Buckman Labor Inc | |
| US4448839A (en) * | 1981-10-16 | 1984-05-15 | Rohm And Haas Company | Method of sizing hydrophobic yarn |
| US4413080A (en) * | 1982-06-21 | 1983-11-01 | Minnesota Mining And Manufacturing Co. | Water-dispersible pressure-sensitive adhesive and tape made therewith |
| JPS6060172A (ja) * | 1983-09-13 | 1985-04-06 | Takamatsu Yushi Kk | 芯地用の粉状熱接着剤 |
-
1996
- 1996-10-21 DE DE69613982T patent/DE69613982T2/de not_active Expired - Lifetime
- 1996-10-21 DK DK96116910T patent/DK0837176T3/da active
- 1996-10-21 AT AT96116910T patent/ATE203289T1/de not_active IP Right Cessation
- 1996-10-21 ES ES96116910T patent/ES2159339T3/es not_active Expired - Lifetime
- 1996-10-21 EP EP96116910A patent/EP0837176B1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE69613982T2 (de) | 2002-04-04 |
| ATE203289T1 (de) | 2001-08-15 |
| DE69613982D1 (de) | 2001-08-23 |
| DK0837176T3 (da) | 2001-09-24 |
| ES2159339T3 (es) | 2001-10-01 |
| EP0837176A1 (en) | 1998-04-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4440647A (en) | Paint spray booth detackification composition and method | |
| US5049300A (en) | Method of activating acidified NMP to provide an effective paint remover composition | |
| US5759975A (en) | Paint line cleaner | |
| NZ232035A (en) | Melamine-formaldehyde detackifier containing a formaldehyde scavenging agent and use in killing over-sprayed, water insoluble paint | |
| US4111816A (en) | Phosphorus-containing polyester and size compositions | |
| US20040000329A1 (en) | Compositions and methods for paint overspray removal processes | |
| CA2293312A1 (en) | Methods and compositions for treating stickies | |
| US5158807A (en) | Liquid mixtures based on ethylene polymers, a process for producing them and a coating or bonding process in which they are used | |
| WO2004024857A1 (en) | Cleaning composition and cleaning of vehicles | |
| US4759855A (en) | Method for detackification of paint spray operation wastes | |
| EP0837176A1 (en) | Tack-rag | |
| KR19980061916A (ko) | 고기능성 양이온 전착 도장 조성물 및 이의 제조 방법 | |
| US4801397A (en) | Peelable solvent-based coating remover | |
| EP0554865B2 (en) | Use of water-based paint composition | |
| US2892736A (en) | Sizing polyester yarns with an ethylene-maleic interpolymer | |
| DE2934951A1 (de) | Waessrige dispersionen von epoxidverbindungen | |
| US5560860A (en) | Water-based paint spray booth flood sheets and methods of reclaiming paint using the same | |
| JP2578033B2 (ja) | 紙力増強剤 | |
| CA2253607C (en) | Paint line cleaner | |
| DE2060114A1 (de) | Carbaminsaeureester,die als Textilhilfsmittel geeignet sind | |
| CA2031396C (en) | Process to reclaim paint from paint booth flood sheet system | |
| KR100192147B1 (ko) | 인쇄용 조제 | |
| DE19743434A1 (de) | Wäßrige Formulierung auf Basis von Arylsulfonsäure-Formaldehyd-Kondensaten oder sulfoniereten Phenol-Formaldehyd-Kondensaten, Tensiden und organischen Komplexbildnern oder anionischen polymeren Dispergiermitteln und ihre Verwendung | |
| US3843388A (en) | Process for cleaning soiled hydrophobic polyamide and polyester fabrics | |
| GB2231876A (en) | Temporary aqueous coating composition |
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 |
|
| 17P | Request for examination filed |
Effective date: 19970521 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE DE DK ES FR GB IE IT NL SE |
|
| AKX | Designation fees paid |
Free format text: AT BE DE DK ES FR GB IE IT NL SE |
|
| RBV | Designated contracting states (corrected) |
Designated state(s): AT BE DE DK ES FR GB IE IT NL SE |
|
| 17Q | First examination report despatched |
Effective date: 19990617 |
|
| GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
| GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
| GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
| GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
| GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
| RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: BRIEL, WERNER |
|
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| ITF | It: translation for a ep patent filed | ||
| AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE DE DK ES FR GB IE IT NL SE |
|
| REF | Corresponds to: |
Ref document number: 203289 Country of ref document: AT Date of ref document: 20010815 Kind code of ref document: T |
|
| REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
| REF | Corresponds to: |
Ref document number: 69613982 Country of ref document: DE Date of ref document: 20010823 |
|
| REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 |
|
| REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2159339 Country of ref document: ES Kind code of ref document: T3 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DK Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20011021 |
|
| 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: 20011022 |
|
| ET | Fr: translation filed | ||
| REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
| 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 |
|
| EUG | Se: european patent has lapsed |
Ref document number: 96116910.9 |
|
| REG | Reference to a national code |
Ref country code: DK Ref legal event code: EBP |
|
| 26N | No opposition filed | ||
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IE Payment date: 20080929 Year of fee payment: 13 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 20091014 Year of fee payment: 14 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IT Payment date: 20091028 Year of fee payment: 14 |
|
| REG | Reference to a national code |
Ref country code: IE Ref legal event code: MM4A |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20091021 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20101021 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20101021 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20121011 Year of fee payment: 17 Ref country code: FR Payment date: 20121031 Year of fee payment: 17 Ref country code: DE Payment date: 20121018 Year of fee payment: 17 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20121012 Year of fee payment: 17 Ref country code: ES Payment date: 20121017 Year of fee payment: 17 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 20121010 Year of fee payment: 17 |
|
| BERE | Be: lapsed |
Owner name: *BRIEL WERNER Effective date: 20131031 |
|
| REG | Reference to a national code |
Ref country code: NL Ref legal event code: V1 Effective date: 20140501 |
|
| GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20131021 |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 69613982 Country of ref document: DE Effective date: 20140501 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20131021 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20140630 |
|
| 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: 20131031 Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140501 Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20140501 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20131031 |
|
| REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20141107 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20131022 |