WO1992000389A1 - Aqueous emulsion of filmogenic resins for finishing leather and leather splits, and its application process - Google Patents
Aqueous emulsion of filmogenic resins for finishing leather and leather splits, and its application process Download PDFInfo
- Publication number
- WO1992000389A1 WO1992000389A1 PCT/EP1991/001138 EP9101138W WO9200389A1 WO 1992000389 A1 WO1992000389 A1 WO 1992000389A1 EP 9101138 W EP9101138 W EP 9101138W WO 9200389 A1 WO9200389 A1 WO 9200389A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- leather
- foam
- splits
- finishing
- aqueous emulsion
- Prior art date
Links
- 239000010985 leather Substances 0.000 title claims abstract description 67
- 239000000839 emulsion Substances 0.000 title claims abstract description 40
- 238000000034 method Methods 0.000 title claims abstract description 33
- 229920005989 resin Polymers 0.000 title claims abstract description 31
- 239000011347 resin Substances 0.000 title claims abstract description 31
- 230000008569 process Effects 0.000 title claims abstract description 27
- 239000006260 foam Substances 0.000 claims description 34
- 238000001035 drying Methods 0.000 claims description 27
- 239000000126 substance Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000004088 foaming agent Substances 0.000 claims description 13
- 238000005187 foaming Methods 0.000 claims description 9
- 239000003381 stabilizer Substances 0.000 claims description 6
- 239000004872 foam stabilizing agent Substances 0.000 claims description 5
- 238000011282 treatment Methods 0.000 claims description 4
- 229910000831 Steel Inorganic materials 0.000 claims description 2
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 2
- 238000007664 blowing Methods 0.000 claims description 2
- 159000000011 group IA salts Chemical class 0.000 claims description 2
- 239000010959 steel Substances 0.000 claims description 2
- 238000012546 transfer Methods 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 description 27
- 238000003825 pressing Methods 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 238000013461 design Methods 0.000 description 6
- 238000005507 spraying Methods 0.000 description 6
- 239000000020 Nitrocellulose Substances 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 229920001220 nitrocellulos Polymers 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 229920005749 polyurethane resin Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 235000012424 soybean oil Nutrition 0.000 description 3
- 239000003549 soybean oil Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- PKRQLNPRQPABDI-UHFFFAOYSA-N 4-amino-1-octadecoxy-1,4-dioxobutane-2-sulfonic acid;sodium Chemical compound [Na].CCCCCCCCCCCCCCCCCCOC(=O)C(S(O)(=O)=O)CC(N)=O PKRQLNPRQPABDI-UHFFFAOYSA-N 0.000 description 2
- 235000000536 Brassica rapa subsp pekinensis Nutrition 0.000 description 2
- 241000499436 Brassica rapa subsp. pekinensis Species 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 229940088990 ammonium stearate Drugs 0.000 description 2
- JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical compound [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 238000004078 waterproofing Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 235000005489 dwarf bean Nutrition 0.000 description 1
- 244000013123 dwarf bean Species 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000001040 synthetic pigment Substances 0.000 description 1
- 238000007725 thermal activation Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C11/00—Surface finishing of leather
- C14C11/003—Surface finishing of leather using macromolecular compounds
Definitions
- This invention relates to an aqueous emulsion of filmogenic resins for finishing leather and leather splits, and its application process.
- leather will be used to indicate leather as such, leather splits, sheepskin, nappa, whole skins for upholstery, buffed leather and full grain leather.
- the emulsion according to the invention contains one or more foaming agents and one or more foam stabilizers.
- the present invention also relates to a process for applying the aqueous emulsions to leather, said process consisting of foaming the emulsion, applying it continuously in a thin layer to the leather with a roller machine, and drying the film obtained.
- the leather finishing and leather split enhancement industry is still largely based on batch operations involving a large use of labour. There is therefore a tendency to reduce labour costs and increase cycle productivity by using continuous processes. There is also a further tendency to reduce the energy costs of the various operations and to minimize their environmental impact, for example by seeking to limit the use of volatile solvents where possible. It is difficult to obtain excellent results and to follow up this tendency. For example, in continuous finishing with synthetic resins, the so-called napping, it is difficult to obtain good covering of the leather surface, especially in the case of splits, without having to resort to repeated applications or to costly expedients. There is therefore a requirement for new or improved products and processes which enable a high quality of finish, high productivity and a low level of environmental pollution to be simultaneously obtained.
- Finishing processes generally involve many stages (each divided into various steps), and which in the most general case comprise the following: applying a base layer to give the desired coloration (synthetic resins and pigments); - applying a synthetic resin layer to form a suitable substrate for preparing an embossed design (this operation can be combined with the preceding) ; applying a nitrocellulose resin layer to facilitate the pressing operation by eliminating problems of tackiness; pressing to form an embossed design; applying a surface finishing layer (nitrocellulose resins). These stages can be repeated individually or in sequence until the desired quality is obtained.
- Filmogenic compounds are normally applied to leather by one of the three following types of application: 1. "Spray” application This can be carried out both on soft leather and on rigid splits. It is a batch process and is also lengthy in that it requires repeated passes to obtain good covering.
- the filmogenic substance dissolved in a solvent or dispersed in water, is applied in the form of an aerosol with the result that at least 4 ⁇ # of the sprayed substance rebounds off the leather and is dispersed within the surrounding air. This rejected quantity is unrecoverable and has to be eliminated by treatment in suitable purifiers.
- Excessively soft leather is "refused" by the rollers as they rotate in the same direction (and thus with their surfaces moving in opposition at different speeds) .
- aqueous resin dispersions used contain a minimum of 6 ⁇ # of water, with consequent considerable drying problems.
- This consists of applying a thin layer of resin onto a support web consisting of release paper, which is followed by the formation of the film, bonding to the substrate to be finished, generally by pressing, and successive drying or polymerization and removal of the finished substrate, with recovery of the release paper.
- the process can be used for both soft and rigid leather, but the deposited film generally has a thickness of 0.2-0.4 mm, so giving it a plastic appearance, feel and consistency unless special techniques are used by which thicknesses less than 0.1 mm can be applied, but which require specially considered resins (such as polyurethane resins) .
- resins such as polyurethane resins
- the quantity of foaming agent is between 0.5% and 3# of the dry content of the emulsion.
- alkaline salts of. fatty monoamides of sulphosuccinic acid have proved particularly active.
- the quantity of foam stabilizer is between 0.4# and 2% of the dry content of the emulsion according to the invention.
- the water quantity is between 4 ⁇ and 70 and the viscosity is between 1000 and 1500 mPas (Brookfield RVT 2 - 10 r.p.m., 20 ° C) .
- an essential characteristic of the emulsions according to the invention is that they contain a foaming agent and a foam stabilizer.
- the emulsion according to the invention is prepared by simply mixing together the various components normally used for leather finishing.
- filmogenic resins of normal use polyacrylic or polyurethane resins are particularly suitable, however other resins (nitrile, butadiene, styrene, acrylic etc.) are not excluded.
- These resins can be thermoplastic, self-crosslinking or co- crosslinking at variable temperatures not exceeding 100°C, or can contain unsaturations (for example acrylic) and therefore be crosslinkable by radiation (eg. by U.V. light). They enable film to be obtained having excellent mechanical strength (tough and scratch- resistant) , good adhesion to its support, flexibility, softness, feel and the desired aesthetic characteristics.
- the emulsions according to the present invention can also contain a thickener to modify the final rheology of the emulsion and make it suitable for the application.
- the mostly used thickeners include polyacrylic salts and their copolymers, and modified natural polymers, in particular carboxymethylcellulose.
- the emulsions of the invention can also contain any other components required to obtain the desired aesthetic or functional characteristics provided they are properly chosen to ensure maximum compatibility with the aforesaid components so that they do not substantially influence the process.
- dyes include dyes, pigments, waxes, feel modifiers, coalescence agents, crosslinking agents, catalysts, antifermenting agents, antimildew agents etc.
- a high grade of finish is obtained for the leather by treating this with the following process: a) forming a foam by blowing air into an aqueous emulsion of filmogenic resins containing one or more foaming agents and one or more foam stabilizers in quantities such that the sum of said quantities is between 1% and 1% by weight of the dry substance and their weight ratio is between 0.2 and 4; b) applying the foam from step a) to the leather to be treated, using a roller; c) drying the treated leather at a temperature of between 50°C and 90°C; d) subsequent treatments.
- aqueous emulsion according to the invention is introduced into an apparatus known as a "foamer" in which it undergoes intimate contact with air to produce a foam which can be of variable consistency and characteristics.
- the air can be microdispersed to the extent of obtaining a gaseous emulsion.
- the foam characteristics can be adjusted by adjusting the air/compound (volume) ratio (the ratio between the compound volume before and after foaming is known as the "foaming ratio"), and the machine operating parameters.
- the foam density obtained can be between 20 and 900 g/1.
- Foam ratios particularly suitable for the purposes of the present invention are between 1:2 and 1:6.
- the preferred foam ratios are between 1:3 and 1:4, with a corresponding density of 250-350 g/1.
- the foam prepared as described is fed to a roller finishing machine where it is deposited by an oscillating doctor blade onto a rotating steel roller engraved as for rotogravure printing and therefore known as a gravure-type roller.
- the machine can also use a roller of different type engraved in a different pattern.
- the gravure roller rotates in opposition to another roller to uniformly distribute the foam over the leather fed to the machine.
- the leather is collected at the roller exit and fed to the subsequent drying operation.
- the feed rate of the leather within the machine is between 4 and 20 m/min, and typically between 8 and 10 m/min.
- rollers rotating in the same direction can consist of a bank of infrared ray generators, or a conventional hot air oven.
- Drying is generally conducted at a temperature of between 50 ° C and 90°C, and preferably between 70°C and 8 ⁇ °C.
- the drying can also be followed by crosslinking of the resins contained in the used emulsion. This can be done by thermal activation at a temperature not exceeding 100°C or by irradiation by UV light, depending on the type of resins used and on the crosslinking agents and catalysts introduced.
- the final treatment of the leather coated and dried as described comprises the normal operations involving application of the intermediate resin layer, pressing to obtain embossed decorations and, where necessary, final varnishing with possibly nitrocellulose- based resin solutions.
- This greater effectiveness of the process according to the invention compared with conventional methods means that a smaller number of passes are used to obtain the required characteristics (for example one pass is generally sufficient to obtain complete coverage with a formulation for base colouring) .
- Very thin and completely transparent films can be obtained (reduced resin consumption) , while at the same time ensuring maximum covering uniformity and mechanical strength. In the case of splits, this for example enables excellent coverage to be obtained in a single pass with the application of a very small quantity of emulsion, this being obtainable in the known art only by using a preliminary rotopressing operation (to reduce the permeability and hence the emulsion absorption) .
- e It is possible to apply with a single pass a much higher emulsion quantity than that applied in the known art. Whatever
- VESLIC rubbing resistance dry and wet, to IUF 450: high Hot iron resistance: 200-220 C
- the compound required for the base coating and pressing operations is prepared by mixing together the following compounds by mechanical stirring in the stated order:
- pigment content 10 dry content 15%
- Foaming agent (35% sodium octadecyl sulpho- succinamate in water) 3 parts
- the compound prepared in this manner has a viscosity of 1300 mPas (Brookfield 2/10 r.p.m. at 20 ° C) .
- Foaming
- the set foaming ratio is 1:3. to obtain a foam of density 3 0 g/1. c.
- the thickness of the foam deposited by the doctor blade on the applicator roller is 0.5 mm, the application being in one pass at 5 m/min.
- Example 2 passes to deposit a total of 100 g/m of dry substance on the split, which is not rotopressed.
- d. The traditional finishing operations are carried out as under point e of Example 1.
- Example 1 Drying as in Example 1, point d, but at 5 m/min. d. The traditional finishing operations are carried out as under point e of Example 1.
- VESLIC rubbing resistance IUF 450
- dry felt/dry leather 500 490 495 b- wet felt/dry leather 150 (1) 145 (2) 148 (2)
- EXAMPLE 4 Foam application system for base covering and resin, intermediate and layer and finish.
- Foaming agent (35% sodium octadecyl sulpho- succinamate in water) 1.2 parts
- Foam stabilizer (25% ammonium stearate in water) 1.5 parts 5- 35% polyacrylic thickener in soybean oil/white spirit 1 part
- the compound has a viscosity of 1500 mPa.s (Brookfield RVT 2 - 10 g/min 20 ° C) 1?
- the buffed goatskin is treated in the machine previously described in the general part of the invention as in Example 1), with a 0.6 mm thickness of foam deposited on the applicator roller, using 1
- Example 2 passes, depositing a total of 150 g/m of dry substance.
- e Drying in a hot air oven (60 C) at a rate of 5 m/min.
- f Rotopressing, spraying of final coating, drying, drumming and final rotopressing are carried out, as in Example 5.
- points e, f, g. h, i On examining the articles obtained in Examples 5 and 6 it can be seen that both have good coverage (a 50X microscopic examination shows a more uniform pigment distribution for Example 5) • The surface is more opaque in Example 5. which is an advantage in garments.
- the comparison shows that using the method of Example 5 the application of the waterproofing base coating can be dispensed with, the base compound can be applied in a smaller number of passes, and the drying time can be reduced.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT02080090A IT1249019B (it) | 1990-06-28 | 1990-06-28 | Emulsione acquosa di resine filmogene per la finitura di pelli, cuoio e croste di pelle e relativo procedimento di applicazione |
IT20800A/90 | 1990-06-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1992000389A1 true WO1992000389A1 (en) | 1992-01-09 |
Family
ID=11172256
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1991/001138 WO1992000389A1 (en) | 1990-06-28 | 1991-06-20 | Aqueous emulsion of filmogenic resins for finishing leather and leather splits, and its application process |
Country Status (3)
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5234913A (en) * | 1991-03-06 | 1993-08-10 | Burroughs Wellcome Co. | Antiviral nucleoside combination |
DE4230997A1 (de) * | 1992-09-16 | 1994-03-24 | Sandoz Ag | Spritzbeständiger wässriger Schaum, dessen Herstellung und Verwendung |
KR20030017835A (ko) * | 2001-08-23 | 2003-03-04 | 주식회사 덕인 | 회전 마스크 패턴을 사용한 에스엘에스 공정 방법 및 그장치 |
ITUA20161537A1 (it) * | 2016-03-10 | 2017-09-10 | Ge Ma Ta Spa | Linea per rifinire pelli che avanzano in modo continuo ed automatico per l'intero ciclo di rifinizione |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2129567A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1971-03-12 | 1972-10-27 | Rohm & Haas | |
CH542665A (de) * | 1970-09-22 | 1973-11-30 | Sandoz Ag | Verfahren zur Nassbehandlung von porösen Materialien aus Kunststoff oder Leder |
-
1990
- 1990-06-28 IT IT02080090A patent/IT1249019B/it active IP Right Grant
-
1991
- 1991-06-20 AU AU80953/91A patent/AU8095391A/en not_active Abandoned
- 1991-06-20 WO PCT/EP1991/001138 patent/WO1992000389A1/en unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH542665A (de) * | 1970-09-22 | 1973-11-30 | Sandoz Ag | Verfahren zur Nassbehandlung von porösen Materialien aus Kunststoff oder Leder |
FR2129567A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1971-03-12 | 1972-10-27 | Rohm & Haas |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5234913A (en) * | 1991-03-06 | 1993-08-10 | Burroughs Wellcome Co. | Antiviral nucleoside combination |
DE4230997A1 (de) * | 1992-09-16 | 1994-03-24 | Sandoz Ag | Spritzbeständiger wässriger Schaum, dessen Herstellung und Verwendung |
US6303665B1 (en) | 1992-09-16 | 2001-10-16 | Clariant Finance (Bvi) Limited | Spray-resistant aqueous foam, its production and use |
KR20030017835A (ko) * | 2001-08-23 | 2003-03-04 | 주식회사 덕인 | 회전 마스크 패턴을 사용한 에스엘에스 공정 방법 및 그장치 |
ITUA20161537A1 (it) * | 2016-03-10 | 2017-09-10 | Ge Ma Ta Spa | Linea per rifinire pelli che avanzano in modo continuo ed automatico per l'intero ciclo di rifinizione |
Also Published As
Publication number | Publication date |
---|---|
IT9020800A1 (it) | 1991-12-28 |
IT1249019B (it) | 1995-02-11 |
IT9020800A0 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1990-06-28 |
AU8095391A (en) | 1992-01-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3930921A (en) | Method of finishing leather | |
US5171494A (en) | Method of producing a paint which on application imparts a surface with a tanned skin or leather-like appearance | |
US3434861A (en) | Process for forming decorative patterns | |
US20240384362A1 (en) | Method for Upgrading and Embossing Leather | |
US2837440A (en) | Method of producing air pervious material by treating with gas evolving blowing agent and coacting with a washable salt layer | |
KR101169744B1 (ko) | 기재용 표면코팅제, 이의 제조 방법 및 이를 이용한 표면처리 방법 | |
US4932978A (en) | Process and apparatus for automatic finishing of flexible materials, and particularly leathers and hides | |
WO1992000389A1 (en) | Aqueous emulsion of filmogenic resins for finishing leather and leather splits, and its application process | |
US2383598A (en) | Decorative surfacing material | |
JPH0832920B2 (ja) | 皮革の化粧仕上げ方法 | |
US20020114925A1 (en) | Coated, flexible flat material | |
US3429727A (en) | Process for making synthetic suede sheet material | |
PL82378B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
US2485967A (en) | Manufacture of patent leather and simulated patent leather | |
RU2800263C1 (ru) | Способ и устройство отделки натуральной кожи | |
JP3391885B2 (ja) | 皮革様シート状物とその製造方法 | |
JPH0693572A (ja) | 複合模造皮革を外観が天然皮革に類似するシート材料に変換する方法 | |
JPH04333674A (ja) | 皮革様シート状物及びその製造方法 | |
WO2024062358A1 (en) | Method of production of a revitalized and ennobled laminar product starting from leather waste | |
US2159639A (en) | Artificial leather manufacture | |
CS197075B1 (cs) | Způsob souběžné výroby alespoň dvou druhů ohebných plošných materiálů | |
KR20220132833A (ko) | 폐 가죽과 폐 섬유의 재활용법 | |
CN119121652A (zh) | 一种超纤合成革及其生产方法 | |
US1190807A (en) | Material adapted for use in the manufacture of an imitation leather and method of making the same. | |
CN113736930A (zh) | 一种环保型高光压摔磨砂革的制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AU BB BG BR CA FI HU JP KP KR LK MC MG MW NO RO SD SU US |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE BF BJ CF CG CH CI CM DE DK ES FR GA GB GN GR IT LU ML MR NL SE SN TD TG |
|
NENP | Non-entry into the national phase |
Ref country code: CA |