SU460633A3 - The method of obtaining artificial leather - Google Patents
The method of obtaining artificial leatherInfo
- Publication number
- SU460633A3 SU460633A3 SU1459294A SU1459294A SU460633A3 SU 460633 A3 SU460633 A3 SU 460633A3 SU 1459294 A SU1459294 A SU 1459294A SU 1459294 A SU1459294 A SU 1459294A SU 460633 A3 SU460633 A3 SU 460633A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- artificial leather
- solution
- thickness
- fibrous
- polyurethane
- Prior art date
Links
Classifications
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
- D04H1/64—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
- D04H1/655—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions characterised by the apparatus for applying bonding agents
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/425—Cellulose series
- D04H1/4258—Regenerated cellulose series
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/4334—Polyamides
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
- D04H1/587—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives characterised by the bonding agents used
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
- D04H1/64—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
- D04H1/645—Impregnation followed by a solidification process
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- 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
- D06N3/0086—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the application technique
-
- 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
- D06N3/0086—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the application technique
- D06N3/0088—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the application technique by directly applying the resin
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
- Y10T428/24438—Artificial wood or leather grain surface
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249924—Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
- Y10T428/249933—Fiber embedded in or on the surface of a natural or synthetic rubber matrix
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Description
1one
Известен опособ получени искусственной кожи путем многократного нанесени «а пропитанную св зующим волокнистую подложку сло раствора полиуретана или его смеси с другими полимерами с возрастающей концентрацией , коагул ции, промывки и последующей сушки; «а этом хот .и достигаетс разна плотность полиуретана по сло м лицевого покрыти , но искусственна .кожа по структуре и свойствам не похожа на натуральную .A method for producing artificial leather is known by repeatedly applying a fiber layer of a solution of polyurethane or its mixture with other polymers with increasing concentration impregnated with a binder, coagulation, washing and subsequent drying; “But although this achieves a different density of polyurethane across the layers of the front coating, but artificial skin is not similar to natural in its structure and properties.
С целью получени искусственной кожи по структуре и свойствам близкой к натуральной коже согласно изобретению каждый последующий слой раствора полиуретана (или его смеси с другими полимерами) нанос т после полного впитывани волокнистым матом предыдущего сло раствора полимера.For the purpose of obtaining artificial leather, according to the structure and properties close to natural leather according to the invention, each subsequent layer of polyurethane solution (or its mixture with other polymers) is applied after the fiber layer is completely absorbed by the fibrous mat.
В качестве исходного материала примен ют волокнистые маты, включающие не менее 1 ч. синтетических волокон и имеющие плотность 0,08-0,30, главным образом 0,12- 0,20 г/см. Такие маты готов т на кардочесальной машине или при бумагоделательном способе и уплотн ют путем нагревани .Fibrous mats comprising at least 1 part of synthetic fibers and having a density of 0.08-0.30, mainly 0.12-0.20 g / cm, are used as the starting material. Such mats are prepared on a carding machine or papermaking process and compacted by heating.
Концентраци эластомерных pacTBOipOB 8- 35, преимущественно 12-30 вес. %. Концентрацию отдельных растворов, наносимых последовательно друг за другом, выбирают в соответствии с плотностью волокнистых матов , чтобы готовый продукт имел возможно большее различие в плотности верхних и нижних сторон.The concentration of elastomeric pacTBOipOB is 8-35, preferably 12-30 wt. % The concentration of the individual solutions, applied successively one after the other, is chosen in accordance with the density of the fibrous mats so that the final product has the greatest possible difference in the density of the upper and lower sides.
Дл изготовлени искусственной кожи с возможно (более плотной верхней стороной, т. е. со структурой наиболее близко подход щей к структуре натуральной кожи, дополнительно ввод т уплотнение волокнистых матов во врем каогул ции эластомеров. При этомFor the manufacture of artificial leather with a possible (more dense upper side, i.e., with the structure most closely resembling the structure of natural leather, the compaction of fibrous mats is additionally introduced during the coagulation of elastomers.
действуют таким образом, что после начала коагул ции эластомерного св зующего ;вещества пропитанные волокнистые маты сжимают в вод ной ванне вращающимис валками. Этот процесс может быть повторен несколькоact in such a way that after the onset of coagulation of the elastomeric binder; the substances impregnated fibrous mats are compressed in a water bath with rotating rollers. This process can be repeated several times.
раз. Таким образом плотность верхней стороны готовой искусственной кожи можно увеличить «а 30-60% по сравнению с несжатой кожей. В качестве пропиточного средства примен ют главным образом растворы полиуретана в диметилформамиде или другие известные растворители. Дл улучшени грифа и гибкости искусственной кожи можно добавл ть в раствор эластомеров (А) 5-30 вес. % парафинового или сил конового (по отношению к эластомеру). Наносимые на верхнюю сторону растворы эластомеров могут содержать до 35 вес. % поливинилхлорида или сополимеров поливинилхлорида по отношению к общему содержанию полимеров, такимtime. Thus, the density of the upper side of the finished imitation leather can be increased by 30-60% compared to uncompressed leather. Solutions of polyurethane in dimethylformamide or other known solvents are mainly used as an impregnating agent. To improve the neck and flexibility of artificial leather, you can add 5-30 weight to the elastomer solution (A). % paraffin or horse force (relative to the elastomer). The elastomer solutions applied on the upper side can contain up to 35 wt. % of polyvinyl chloride or copolymers of polyvinyl chloride with respect to the total content of polymers, such
образом повышаетс термостабилизаци материала , что имеет особое значение при дальнейшей переработке искусственной кожи в обувной промышленности.the thermal stabilization of the material is enhanced, which is of particular importance in the further processing of artificial leather in the shoe industry.
Пример 1. На бумагоделательной машине :изготовл 1от прочес из дисперсил полиамидного и регенери|рова1нного целлюлозного волокна (соотношение 80:20). Этот прочес уплотн ют путем кратковременного «апревани .Example 1. On a paper machine: 1 fabric was made from polyamide and regenerated cellulose fiber dispersion (80:20 ratio). This batt is compacted by short-term heating.
Дл пропитки прочеса примен ют эластомерНые растворы А-С следуюш;его состава, вес. %: Полиуретан Диметилформамид Силиконовое масло Сополимеры винилхлорида и малеинового ангидрида Вода Примен емый во всех растворах полиуретан вл етс продуктом преобразовани полибутиленадипата со средним молекул рным весом около 1000, дифенилметан-4,4-диизоцианата н бутандиола в мол рном соотношении 1 :3, 10:2,1. Силиконовое масло вл етс фенил метил пол,исилоксаном. PacTBOipbi нагревают до 45°С и дегазируют. Волокнистый ирочес подвод т к валковой ракле со скоростью 1 м/мин. Валик двигают в ванне, наполнениой раствором А. Р дом с местом соприкосновени валка и «ижней стороны прочеса устанавливают на некотором ра-осто ии от поверхности валка скребок, KOTOipbm срезает раствор до толш,и.ны сло 0,5 мм. Переносимый на «ижнюю сторону прочеса раствор пропитывающего средства составл ет около 0,5 кг на 1 м прочеса. Посредством ракли, установленной на высоте оси валика над прочесом, одновременно нанос т раствор В. Зазор между раклей и верхней стороной прочеса составл ет 0,6 мм. На квадр.атный метр волокнистого мата нанос т 0,77 кг раствора В. Прочес провод т свободно за раклей 0,6 м, а затем пропускают между парой валков. До поступлени прочеса в валки раствор В полностью проникает в волокнистый мат, который выгл дит волОКнистым и почти сухим. Валки привод т в движение с окружной скоростью вращени 1 м/мин зазор между валка 1и 2,1 мм, поэтому не происходит отжима пропитывающего раствора. На рассто нии 0,5 -м за этой парой валко-в прочес подвод т к следующей ракле, котора установлена на рассто нии 0,7 мм от верхней поверхности прочеса, и нанос т 0,8 «г раствора С на 1 м волокнистого мата. На рассто нии 2 м за валковой раклей прочес поступает в вод ную ванну с температурой 40° С, в которой коагулируют полимеры и вымывают растворитель, затем прочес высушивают.For impregnation through the web, elastomer solutions A – C are used as follows; its composition, wt. %: Polyurethane Dimethylformamide Silicone oil Vinyl chloride / maleic anhydride copolymers Water Polyurethane used in all solutions is a product of polybutylene adipate with an average molecular weight of about 1000, diphenylmethane-4,4-diisocyanate and butane diol in a molar ratio of 1: 3, 3, 3, 3, 3, 3, 3, 3, 3, butanediol in a 1: 3, 3, 3, 3 molar ratio, 1: 3, 3, 3, 3-diisocyanate and butane diol in a molar ratio of 1: 3, 3, 3, 3, 3, 3, 3 2.1. Silicone oil is phenyl methyl field, isiloxane. PacTBOipbi is heated to 45 ° C and degassed. Fibrous iriches are fed to the roll doctor at a speed of 1 m / min. The roller is moved in the bath, filled with solution A. Next to the place of contact between the roll and the upper side of the batt, the scraper is installed on some work from the surface of the roll, KOTOipbm cuts the solution to thickness, and 0.5 mm of a layer. The impregnating solution batt transported to the bottom side is about 0.5 kg per meter of impregnation. By means of a doctor blade installed at the height of the roller axis above the batt, solution B is applied simultaneously. The gap between the doctor blade and the batt upper side is 0.6 mm. 0.77 kg of solution B is applied per square meter of fibrous mat. The webbing is carried out freely with a 0.6 m squeegee and then passed between a pair of rolls. Before the batting in the rollers, solution B completely penetrates into the fibrous mat, which looks volOKnisty and almost dry. The rolls are set in motion with a circumferential speed of rotation of 1 m / min. The gap between the roll 1 and 2.1 mm, so that the impregnating solution does not spin. At a distance of 0.5 m behind this pair of rolls, the next blade, which is set at a distance of 0.7 mm from the top surface of the batt, is applied to the next blade, and 0.8 г g of solution C is applied to 1 m of fiber mat. . At a distance of 2 m behind a rollerblade, the batt enters a water bath with a temperature of 40 ° C, in which the polymers coagulate and wash off the solvent, then the batt is dried.
Пример 2. Повтор ют способ, описанный в примере 1, примен волокнистый прочес указанного состава. Наносимые последовательно друг за другом полимерные {растворы А-С имеют следующий состав, вес.%:Example 2. The method described in Example 1 is repeated using a fiber batt of the composition indicated. Polymeric {solutions A – C, applied successively one after another, have the following composition, wt.%:
ВСThe sun
Полиуретан16,0Polyurethane16,0
18,0 20,018.0 20.0
Парафиновое масло2,0Paraffin oil2.0
6,0 6.0
4,04.0
Вода6,0Water6.0
Диметилформамид76,0 76,0Dimethylformamide 76.0 76.0
71,071.0
5,05.0
Сополимеры винилхлорида- Полиуретан получают путем превращени полпбутиленадипата, днфенилмета|Н-4,4-ди (Изоцианата и бутандиола в соотношении 1 :2: : 1. После нанесени раствора в соответствии с примером 1 пропитанный прочес без применени сжати во врем коагул ции пропускают через вод ную ванну. Вес 1 м искусственной кожи 775 г и толщина 1,29 мм. Плотность трех слоев толщиной до 0,43 мм составл . ет снизу BBQpx 0,52, 0,60, 0,68 г/см. Пример 3. Из волокнистого прочеса (пример 1) изготовл ют искусственную кожу путем пропитки согласно примеру 1, причем наносимые последовательно друг за другом растворы А-С имеют следующий состав, вес. %: Полиуретан Парафиновое масло Вода Диметилфор.мамид Сополимеры винилхлорида Полиуретан получают путем превращени полибутил енадипата, дифенилметан-4,4-диизоцианата и бутандиола в соотношении 1 : : 2,5: 1,5. Процесс коагул ции провод т без применени сжати . Вес 1 м искусственной кожи 778 г, толщина 1,73 мм. Три сло толщи1ной по 0,58 iMM имеют плотность 0,33, 0,46 и 0,56 Г/1СМ. Пример 4. Волокнистый прочес (пример 1) пропитывают, как в примере 1, растворами А-С следующего состава, вес. %: ВС Полиуретан12,0 16,0 20,0 Парафиновое масло2,0 Вода6,0 Диметилформамид80,0 Сополимеры винилхлорлда- Полиуретан получают путем превращени полибутиленадипата, дифенилметан-4,4-диизоцианата и бутандиола в соотношении 1 : :2,25: 1,25. После обработки пропитанного волокнистого мата дл коагул ции пол1име|ров безVinyl chloride-Copolymers Polyurethane is obtained by converting polybutylene adipate, dnfenilmeta | H-4,4-di (Isocyanate and butanediol in a ratio of 1: 2: 1. After applying the solution in accordance with Example 1, the impregnated bat without compression during coagulation is passed through water bath. The weight of 1 m of artificial leather is 775 g and the thickness is 1.29 mm, The density of three layers with a thickness of up to 0.43 mm is below BBQpx 0.52, 0.60, 0.68 g / cm. Example 3. Artificial skin is made of a fibrous bat (Example 1) by impregnation according to Example 1, and successively one after another, the A-C solutions have the following composition, wt%: Polyurethane Paraffin oil Water Dimethylformamide Vinyl chloride copolymers Polyurethane is obtained by converting polybutyl enadipate, diphenylmethane-4,4-diisocyanate and butanediol in a ratio of 1: 2.5: 1.5. The coagulation process is carried out without the use of compression. The weight of 1 m of artificial leather is 778 g, thickness is 1.73 mm. Three layers of 0.58 iMM each have a density of 0.33, 0.46 and 0.56 G / 1CM Example 4. Fibrous webs (example 1) are impregnated, as in example 1, with solutions A – C of the following composition, weight. %: Sun Polyurethane12.0 16.0 20.0 Paraffin oil2.0 Water6.0 Dimethylformamide 80.0 Vinylchloride-Copolymers Polyurethane is obtained by converting polybutylene adipate, diphenylmethane-4,4-diisocyanate and butanediol in a ratio of 1: 2.25: 1 25 After processing the impregnated fiber mat to coagulate the polymers without
применени сжати у готовой и€кусствен«ой кожи получены следующие показатели: вес 1 м 885 г, толщина 2,40 мм. Три сло толщиной 0,80 мм имеют плотность 0,29, 0,36 и 0,45 г/см.the use of compression in the finished and body leather obtained the following indicators: weight 1 m 885 g, thickness 2.40 mm. Three layers with a thickness of 0.80 mm have a density of 0.29, 0.36 and 0.45 g / cm.
Если коагул цию тровод т лод давлением, то получают искуоственную кожу, вес 1 м который составл ет 874 г, толщина 1,62 мм. Слои толщиной по 0,54 мм имеют плотность 0,41, 0,50 и 0,63 г/смз.If the coagulation is carried out by pressure, artificial skin is obtained, the weight of 1 m which is 874 g, the thickness is 1.62 mm. Layers with a thickness of 0.54 mm have a density of 0.41, 0.50 and 0.63 g / cm 3.
Пример 5. Волок1нистый прочес толщиной 1,85 мм подвергают .прописке согласно примеру 1 растворами, имеющими состав, указанный в примере 4. Легко уплотненна во врем коагул ции искусственна кожа имеет толщину 1,31 мм и вес 1 м 687 г. .Слои толщиной по 0,41 мм обладают плотностью 0,47, 0,52 и 0,67 г/смз.Example 5. The fibrous webs with a thickness of 1.85 mm are subjected to a prescription according to example 1 with solutions having the composition specified in example 4. The artificial skin is easily compacted during coagulation and has a thickness of 1.31 mm and a weight of 1 m 687 g. Layers of 0.41 mm each have a density of 0.47, 0.52 and 0.67 g / cm3.
Пример 6. Волокнистый мат подвергают цропитке, «ак указано в примере 1. Последовательно используемые дл этого растворыExample 6. A fibrous mat is subjected to an imbalance, “as indicated in Example 1. The solutions sequentially used for this
имеют состав, как в п-римере 2. Коагул цию полимеров .провод т без сжати . Вес 1 м искусственной КОЖ.И 705 г, толщина 1,31 мм. Слои имеют толщину 0,44 мм каждый и обладает плотностью 0,48, 0,52 .и 0,62 г/см.have a composition as in p-polymer 2. Coagulation of polymers is carried out without compression. Weight of 1 m of artificial leather. And 705 g, thickness 1.31 mm. The layers have a thickness of 0.44 mm each and have a density of 0.48, 0.52, and 0.62 g / cm.
Предмет изобретени Subject invention
Способ получени искусственной кожи путем многократного нанесени на волокнистый холст слоев раствора в органическом растворителе полиуретана или его смеси с винилхларидным полимером с возрастающей концентрацией от сло к слою, коагул ции «мокрым методом, промывки и сушки, о тличающийс тем, что, с целью получени искусственной кожи по структуре ai свойствам близкой к натуральной коже, каждый последующий слой раствора нанос т на волокнистый холст после полного впитывани им предыдущего сло раствора полимера.The method of obtaining artificial leather by repeatedly applying to the fibrous canvas layers of a solution in an organic solvent of polyurethane or its mixture with vinyl chloride polymer with increasing concentration from layer to layer, coagulating with a wet method, washing and drying, in order to obtain artificial skin on the ai structure properties close to natural leather, each subsequent layer of the solution is applied to the fibrous canvas after it has completely absorbed the previous layer of the polymer solution.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19691936073 DE1936073C3 (en) | 1969-07-16 | Process for the production of artificial leather similar to natural leather |
Publications (1)
Publication Number | Publication Date |
---|---|
SU460633A3 true SU460633A3 (en) | 1975-02-15 |
Family
ID=5739926
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1459294A SU460633A3 (en) | 1969-07-16 | 1970-07-15 | The method of obtaining artificial leather |
Country Status (19)
Country | Link |
---|---|
US (1) | US3672943A (en) |
JP (1) | JPS4948482B1 (en) |
AT (1) | AT309088B (en) |
AU (1) | AU449513B2 (en) |
BE (1) | BE750989A (en) |
CA (1) | CA922181A (en) |
CH (1) | CH533201A (en) |
CS (1) | CS151560B2 (en) |
DK (1) | DK136222C (en) |
ES (1) | ES380405A1 (en) |
FI (1) | FI53326C (en) |
FR (1) | FR2051784B1 (en) |
GB (1) | GB1307294A (en) |
IE (1) | IE34115B1 (en) |
IL (1) | IL34476A (en) |
LU (1) | LU61332A1 (en) |
NL (1) | NL7008046A (en) |
NO (1) | NO129304B (en) |
SU (1) | SU460633A3 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3928627A (en) * | 1971-07-22 | 1975-12-23 | Walter E Heller Factors Inc | Decorative wall covering |
SE383007B (en) * | 1973-03-02 | 1976-02-23 | Svenska Cellulosa Ab | METHOD OF PRODUCING SURFACE TREATED PAPER IN THE FORM OF A CONTINUOUS PATH |
JPS5848579B2 (en) * | 1974-10-03 | 1983-10-29 | テイジンコ−ドレ カブシキガイシヤ | Bitako Seishi - Tozairiyouno Seizouhou |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4827442B1 (en) * | 1965-05-10 | 1973-08-22 |
-
1970
- 1970-04-24 IE IE522/70A patent/IE34115B1/en unknown
- 1970-04-30 CA CA081603A patent/CA922181A/en not_active Expired
- 1970-05-04 GB GB2134270A patent/GB1307294A/en not_active Expired
- 1970-05-05 FI FI126370A patent/FI53326C/en active
- 1970-05-05 NO NO01718/70A patent/NO129304B/no unknown
- 1970-05-05 IL IL3447670A patent/IL34476A/en unknown
- 1970-05-05 DK DK227070A patent/DK136222C/en active
- 1970-05-08 AU AU14707/70A patent/AU449513B2/en not_active Expired
- 1970-05-15 CH CH725870A patent/CH533201A/en not_active IP Right Cessation
- 1970-05-22 AT AT460170A patent/AT309088B/en active
- 1970-05-27 BE BE750989D patent/BE750989A/en unknown
- 1970-06-03 NL NL7008046A patent/NL7008046A/xx unknown
- 1970-06-04 ES ES380405A patent/ES380405A1/en not_active Expired
- 1970-07-14 LU LU61332D patent/LU61332A1/xx unknown
- 1970-07-14 US US54787A patent/US3672943A/en not_active Expired - Lifetime
- 1970-07-15 SU SU1459294A patent/SU460633A3/en active
- 1970-07-15 CS CS497870A patent/CS151560B2/cs unknown
- 1970-07-16 JP JP6183470A patent/JPS4948482B1/ja active Pending
- 1970-07-16 FR FR7026104A patent/FR2051784B1/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DK136222B (en) | 1977-09-05 |
BE750989A (en) | 1970-11-03 |
ES380405A1 (en) | 1972-09-01 |
IE34115B1 (en) | 1975-02-05 |
JPS4948482B1 (en) | 1974-12-21 |
CH533201A (en) | 1973-01-31 |
DE1936073A1 (en) | 1971-02-25 |
AU449513B2 (en) | 1974-05-31 |
GB1307294A (en) | 1973-02-14 |
FI53326C (en) | 1978-04-10 |
DE1936073B2 (en) | 1976-11-04 |
NL7008046A (en) | 1971-01-19 |
LU61332A1 (en) | 1970-09-14 |
IE34115L (en) | 1971-01-16 |
AU1479770A (en) | 1971-11-18 |
IL34476A0 (en) | 1970-07-19 |
IL34476A (en) | 1974-06-30 |
DK136222C (en) | 1978-02-06 |
FI53326B (en) | 1977-12-30 |
NO129304B (en) | 1974-03-25 |
AT309088B (en) | 1973-08-10 |
FR2051784A1 (en) | 1971-04-09 |
FR2051784B1 (en) | 1974-05-03 |
CS151560B2 (en) | 1973-10-19 |
CA922181A (en) | 1973-03-06 |
US3672943A (en) | 1972-06-27 |
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