EP3266914B1 - Tissu composite renforcé et son procédé de fabrication - Google Patents
Tissu composite renforcé et son procédé de fabrication Download PDFInfo
- Publication number
- EP3266914B1 EP3266914B1 EP17152774.0A EP17152774A EP3266914B1 EP 3266914 B1 EP3266914 B1 EP 3266914B1 EP 17152774 A EP17152774 A EP 17152774A EP 3266914 B1 EP3266914 B1 EP 3266914B1
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- EP
- European Patent Office
- Prior art keywords
- thermoplastic elastomeric
- hardness
- hardness thermoplastic
- low
- yarn
- Prior art date
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- 239000004744 fabric Substances 0.000 title claims description 127
- 239000002131 composite material Substances 0.000 title claims description 79
- 238000000034 method Methods 0.000 title claims description 41
- 229920001169 thermoplastic Polymers 0.000 claims description 158
- 239000004416 thermosoftening plastic Substances 0.000 claims description 158
- 229920002725 thermoplastic elastomer Polymers 0.000 claims description 144
- 229920000642 polymer Polymers 0.000 claims description 117
- 238000002844 melting Methods 0.000 claims description 38
- 230000008018 melting Effects 0.000 claims description 38
- 238000007731 hot pressing Methods 0.000 claims description 30
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims description 29
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 29
- 229920001971 elastomer Polymers 0.000 claims description 24
- 239000000806 elastomer Substances 0.000 claims description 24
- 239000000835 fiber Substances 0.000 claims description 15
- 239000012783 reinforcing fiber Substances 0.000 claims description 11
- 238000009941 weaving Methods 0.000 claims description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
- 238000002074 melt spinning Methods 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 6
- 229920006285 olefinic elastomer Polymers 0.000 claims description 6
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 229920006342 thermoplastic vulcanizate Polymers 0.000 claims description 5
- 229920006345 thermoplastic polyamide Polymers 0.000 claims description 4
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 2
- 229920000271 Kevlar® Polymers 0.000 claims description 2
- 239000004917 carbon fiber Substances 0.000 claims description 2
- 239000003365 glass fiber Substances 0.000 claims description 2
- 239000004761 kevlar Substances 0.000 claims description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 2
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 claims description 2
- 239000002759 woven fabric Substances 0.000 description 43
- 239000004753 textile Substances 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 14
- 229920000728 polyester Polymers 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 239000012744 reinforcing agent Substances 0.000 description 6
- 229920002943 EPDM rubber Polymers 0.000 description 5
- 239000004831 Hot glue Substances 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 230000003014 reinforcing effect Effects 0.000 description 4
- 229920003232 aliphatic polyester Polymers 0.000 description 3
- 125000005442 diisocyanate group Chemical group 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 229920002367 Polyisobutene Polymers 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 229920003049 isoprene rubber Polymers 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003733 fiber-reinforced composite Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229920003212 trans-1,4-polyisoprene Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/50—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D1/00—Woven fabrics designed to make specified articles
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/20—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads
- D03D15/283—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the material of the fibres or filaments constituting the yarns or threads synthetic polymer-based, e.g. polyamide or polyester fibres
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/50—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads
- D03D15/587—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads adhesive; fusible
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2101/00—Inorganic fibres
- D10B2101/02—Inorganic fibres based on oxides or oxide ceramics, e.g. silicates
- D10B2101/06—Glass
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2101/00—Inorganic fibres
- D10B2101/10—Inorganic fibres based on non-oxides other than metals
- D10B2101/12—Carbon; Pitch
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2321/00—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D10B2321/02—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2321/00—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D10B2321/02—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins
- D10B2321/021—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins polyethylene
- D10B2321/0211—Fibres made from polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds polyolefins polyethylene high-strength or high-molecular-weight polyethylene, e.g. ultra-high molecular weight polyethylene [UHMWPE]
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
- D10B2331/02—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyamides
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
- D10B2331/02—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyamides
- D10B2331/021—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyamides aromatic polyamides, e.g. aramides
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
- D10B2331/10—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyurethanes
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2505/00—Industrial
- D10B2505/02—Reinforcing materials; Prepregs
Definitions
- the present invention relates to textile technology, and particularly relates to a reinforced composite fabric and a method for preparing a reinforced composite fabric.
- the Europe patent publication 0101305 A2 discloses an oriented woven furniture support material which is a synthetic woven material suitable for use in furniture. Due to the development of technology, the demands for the functional textiles increase. The functional textiles have different properties and functions according to different uses.
- the Japan patent publication H04146235 A provides a woven and knit fabric having excellent crease recovery and durability. In addition to the crease recovery and durability, the mechanical strength is also an important property to the textiles.
- the Europe patent publication 0768406 A1 discloses a fiber-reinforced composite material containing reinforcing fibers and matrix fibers. In the prior arts, reinforced textiles are usually formed by adding a reinforcing agent or attaching a reinforcing film to enhance their strengths.
- reinforcing agent is more widely used between these two means.
- Common reinforcing agents include tear strength improver, rubbing fastness improver, or fabric enhancer. After the textile is immersed in a solution containing the reinforcing agent, a polymer layer is attached onto the surface of the textile, such that the strength of the textile can be enhanced.
- the concentration of the reinforcing agent needs to be lower than 5% to sustain the texture of the reinforced textile, resulting in that the reinforced effect cannot be effectively improved.
- Using the reinforcing agent to enhance the strength requires additional impregnation process and drying process, resulting in a more complicated process, longer processing time, and higher cost.
- large consumptions of water and solvent during the process cause large burdens to the environment, and thus the conventional method is not suitable for the mass production of the reinforced fabrics in the future that people pay attention to the environmental protection increasingly.
- Film lamination is also useful to reinforce the strength of the textile.
- the surface of the textile is dot-coated with a hot melt adhesive solution, and then covered with a reinforcing film to form a laminated structure. Finally, the laminated structure is hot-pressed under 200°C to 300°C to form the reinforced textile.
- the hot melt adhesive layer is aged over time and would peel from the textile, and thus lose the property of high strength.
- the solvent contained in the hot melt adhesive solution might remain in the reinforced textile made by the film lamination, thereby limiting the applicability of the reinforced textile.
- the objective of the present invention is to provide a reinforced composite fabric and a method for preparing a reinforced composite fabric which overcomes the problem of peeling of the reinforcing film and simplifies the fabrication process.
- the present invention provides a method for preparing a reinforced composite fabric including:
- thermoplastic elastomeric yarns with different hardness or different melting points are hot-pressed at a suitable temperature to allow the low-hardness thermoplastic elastomeric yarn to be partially melted and attached on the surface of the high-hardness thermoplastic elastomeric yarn, so as to obtain the reinforced composite fabric.
- the tensile strength and the impact strength are enhanced without using the hot melt adhesive solution.
- the drawbacks of aging of the hot melt adhesive layer, peeling of the reinforcing film, and residuals of the solvent are overcome. Further, the fabrication process of the reinforced fabric is simpler than the prior art.
- the hot-pressing pressure is from 0.0098 MPa to 0.98MPa.
- the hot-pressing temperature is higher than the melting point of the low-hardness thermoplastic elastomeric yarn by 10°C to 50°C.
- the hot-pressing temperature is higher than the melting point of the low-hardness thermoplastic elastomeric yarn by 10°C to 20°C. Therefore, the present invention can hot-press the fabric under a hot-pressing temperature lower than 200°C and make the low-hardness thermoplastic elastomeric yarn partially melted.
- the hot-pressing temperature can be adjusted according to the melting point of the high-hardness thermoplastic elastomeric yarn and the melting point of the low-hardness thermoplastic elastomeric yarn.
- the melting point of the low-hardness thermoplastic elastomeric yarn is from 50°C to 150°C. More preferably, the melting point of the low-hardness thermoplastic elastomeric yarn is from 70°C to 150°C. Therefore, the reinforced composite fabric is made under the lower hot-pressing temperature.
- the melting point of the high-hardness thermoplastic elastomeric yarn is from 150°C to 300°C. More preferably, the melting point of the high-hardness thermoplastic elastomeric yarn is from 160°C to 300°C. Much more preferably, the melting point of the high-hardness thermoplastic elastomeric yarn is from 180°C to 250°C.
- a shore hardness of the low-hardness thermoplastic elastomeric yarn is from 10A to 90A and a shore hardness of the high-hardness thermoplastic elastomeric yarn is from 95A to 90D.
- the method further comprises the step of twisting a high-hardness thermoplastic elastomeric fiber and a reinforcing fiber into the high-hardness thermoplastic elastomeric yarn.
- the step of twisting a high-hardness thermoplastic elastomeric fiber and a reinforcing fiber makes the high-hardness thermoplastic elastomeric yarn have the characteristic of the reinforcing fiber.
- the addition of the reinforcing fiber widens the applicability of the reinforced composite fabric and may enhance the tensile strength and the impact strength of the reinforced composite fabric.
- the reinforcing fiber is a synthetic fiber.
- the applicable synthetic fiber of the present invention includes a carbon fiber, a glass fiber, a Kevlar fiber, or a Dyneema fiber.
- a percentage of the reinforcing fiber ranges from 10 wt% to 90 wt% based on the overall weight of the high-hardness thermoplastic elastomeric yarn.
- the method further comprises the steps of melt spinning a high-hardness thermoplastic elastomeric polymer into the high-hardness thermoplastic elastomeric yarn and of melt spinning a low-hardness thermoplastic elastomeric polymer into the low-hardness thermoplastic elastomeric yarn.
- thermoplastic rubber elastomer TPR
- thermoplastic polyurethane elastomer TPU
- styrene-based thermoplastic elastomer TPS
- thermoplastic olefinic elastomer TPO
- thermoplastic vulcanizate elastomer TPV
- thermoplastic ester elastomer TPEE
- thermoplastic polyamide elastomer TPAE
- the high-hardness thermoplastic elastomeric polymer and the low-hardness thermoplastic elastomeric polymer are classified as the identical thermoplastic elastomeric polymer. Therefore, the reinforced composite fabric may have higher tensile strength and higher impact strength due to the same or better affinity between the high-hardness thermoplastic elastomeric yarn and the low-hardness thermoplastic elastomeric yarn.
- the high-hardness thermoplastic elastomeric polymer and the low-hardness thermoplastic elastomeric polymer each respectfully have a soft segment and a hard segment.
- the hardness and the melting point of the thermoplastic elastomeric polymer may be adjusted according to a ratio of the soft segment to the hard segment.
- the soft segment can be constructed by, but not limited to, butadiene rubber (BR), isoprene rubber (IR), natural rubber (NR), ethylene propylene diene monomer (EPDM), isobutylene isoprene rubber (IIR), polyisobutylene (PIB), polyethylene/polybutylene, amorphous polyethylene, polyether polyol, polyester polyol, or polyester.
- BR butadiene rubber
- IR isoprene rubber
- NR natural rubber
- EPDM ethylene propylene diene monomer
- IIR isobutylene isoprene rubber
- PIB polyisobutylene
- polyethylene/polybutylene amorphous polyethylene
- polyether polyol polyol
- polyester polyol or polyester.
- the hard segment can be constructed by, but not limited to, polystyrene (PS), polyethylene (PE), polypropylene (PP), syndiotactic 1,2-polybutadiene, trans -1,4-polyisoprene, polyurethanes (PU), diisocyanate, or polyamide (PA).
- PS polystyrene
- PE polyethylene
- PP polypropylene
- syndiotactic 1,2-polybutadiene polyurethanes
- PU polyurethanes
- diisocyanate or polyamide (PA).
- the soft segment in the polyester-polyether type of TPEE system, can be constructed by polyether and the hard segment can be constructed by aromatic crystal polyester.
- the soft segment in the polyester-polyester type of TPEE system, can be constructed by aliphatic polyester and the hard segment can be constructed by aromatic crystal polyester.
- the ratio of the soft segment to the hard segment of the high-hardness thermoplastic elastomeric polymer is from 25:75 to 50:50.
- the ratio of the soft segment to the hard segment of the low-hardness thermoplastic elastomeric polymer is from 51:49 to 80:20.
- the high-hardness thermoplastic elastomeric polymer and the low-hardness thermoplastic elastomeric polymer are both TPU.
- the ratio of the soft segment to the hard segment of the high-hardness thermoplastic elastomeric polymer is from 30:70 to 50:50.
- the ratio of the soft segment to the hard segment of the low-hardness thermoplastic elastomeric polymer is from 56:44 to 70:30.
- the high-hardness thermoplastic elastomeric polymer and the low-hardness thermoplastic elastomeric polymer are both TPEE.
- the ratio of the soft segment to the hard segment of the high-hardness thermoplastic elastomeric polymer is from 30:70 to 40:60.
- the ratio of the soft segment to the hard segment of the low-hardness thermoplastic elastomeric polymer is from 52:48 to 75:25.
- the high-hardness thermoplastic elastomeric polymer and the low-hardness thermoplastic elastomeric polymer are both TPO.
- the ratio of the soft segment to the hard segment of the high-hardness thermoplastic elastomeric polymer is from 30:70 to 40:60.
- the ratio of the soft segment to the hard segment of the low-hardness thermoplastic elastomeric polymer is from 55:45 to 75:25.
- the step of forming a high-hardness thermoplastic elastomeric yarn and a low-hardness thermoplastic elastomeric yarn into a fabric by weaving further comprises twisting the high-hardness thermoplastic elastomeric yarn and the low-hardness thermoplastic elastomeric yarn into multiple complex yarns and forming the complex yarns into the fabric.
- Each of the complex yarns comprises foresaid high-hardness thermoplastic elastomeric yarn and low-hardness thermoplastic elastomeric yarn twisted together.
- the high-hardness thermoplastic elastomeric yarn and the low-hardness thermoplastic elastomeric yarn can form the fabric by a weaving method.
- the fabrics can be, but not limited to, circular knitted fabric, knitted fabric, jersey fabric, woven fabric, plain fabric, ribbing fabric, or corrugated fabric.
- the fabrics can be formed by different weaving methods in the same process, for example, the fabric can be formed by knitted weaving in combination with woven weaving and plain weaving.
- the present invention provides a reinforced composite fabric comprising a high-hardness thermoplastic elastomeric yarn and a low-hardness thermoplastic elastomeric yarn. A part of a surface of the low-hardness thermoplastic elastomeric yarn is melted and attached on a surface of the high-hardness thermoplastic elastomeric yarn.
- the reinforced composite fabric can be made by the method mentioned above.
- the reinforced composite fabric and the method for preparing the reinforced composite fabric have advantages as follows.
- Hot-pressing the fabric woven by the high-hardness thermoplastic elastomeric yarn and the low-hardness thermoplastic elastomeric yarn allows the reinforced composite fabric to have a higher tensile strength and a higher impact strength.
- the method for preparing the reinforced composite fabric overcomes the problems to fabricate the reinforced textiles by the intensifiers impregnation and the film lamination.
- the reinforced composite fabric can be hot-pressed under a lower hot-pressing temperature.
- the reinforced composite fabric has a higher tensile strength and a higher impact strength
- the reinforced composite fabric and the method for preparing the same is provided as follows.
- thermoplastic elastomeric (abbreviated as HH-TPE) polymer used in the instant example was thermoplastic polyurethane elastomer (TPU), which had a soft segment and a hard segment at a ratio of 44:56.
- the soft segment was constructed by polyol and the hard segment was constructed by diisocyanate.
- the HH-TPE polymer having a shore hardness of 95A and a melting point of 190°C was melt spun to prepare a HH-TPE yarn (16.7tex /72F).
- a low-hardness thermoplastic elastomeric (abbreviated as LH-TPE) polymer used in the instant example was TPU and had a soft segment and a hard segment at a ratio of 65:35.
- the soft segment was constructed by polyol and the hard segment was constructed by diisocyanate.
- the LH- TPE polymer having a shore hardness of 80A and a melting point of 100°C was melt spun to prepare a LH-TPE yarn (16.7tex /72F).
- the HH-TPE yarn and the LH-TPE yarn were crossed upon each other at a ratio of 1:1 to form a woven fabric.
- the size of the woven fabric was 21 cm ⁇ 30 cm.
- the structure of the woven fabric was shown in Fig. 1 .
- the woven fabric 1A was composed of the HH-TPE yarn 2 and the LH-TPE yarn 3.
- the warp was composed of the HH-TPE yarn 2 and the LH-TPE yarn 3 at a ratio of 1:1
- the weft was composed of the HH-TPE yarn 2 and the LH-TPE yarn 3 at a ratio of 1:1. That is, the HH-TPE yarn 2 and the LH-TPE yarn 3 were staggered together in both lateral direction and vertical direction.
- the woven fabric 1A was preheated under 100°C for half an hour and hot-pressed under 110°C and a pressure of 0.098 MPa for 3 minutes. After cooling the hot-pressed woven fabric, a reinforced composite fabric was finally obtained.
- a HH-TPE yarn (16.7tex/72F) and a LH-TPE yarn (16.7tex/72F) used in the instant example were similar with those in Example 1.
- the HH-TPE yarn and the LH-TPE yarn were crossed upon each other at a ratio of 2: 1 to form a woven fabric.
- the structure of the woven fabric was shown in Fig. 2 .
- the woven fabric 1B was composed of the HH-TPE yarn 2 and the LH-TPE yarn 3.
- the warp was composed of the HH-TPE yarn 2 and the LH-TPE yarn 3 at a ratio of 2:1
- the weft was composed of the HH-TPE yarn 2 and the LH-TPE yarn 3 at a ratio of 2:1. That is, two HH-TPE yarns 2 and one LH-TPE yarn 3 were arranged repeatedly in both lateral direction and vertical direction.
- Example 2 the woven fabric 1B was preheated and hot-pressed as described in Example 1 to form a reinforced composite fabric of Example 2.
- a HH-TPE polymer used in the instant example was thermoplastic polyether ester elastomer (TPEE), which had a soft segment and a hard segment at a ratio of 37:63.
- the soft segment was constructed by aliphatic polyester and the hard segment was constructed by aromatic crystal polyester.
- the HH-TPE polymer having a shore hardness of 72D and a melting point of 220°C was melt spun to prepare a HH-TPE yarn (16.7tex /72F).
- a LH-TPE polymer used in the instant example was TPEE, which had a soft segment and a hard segment at a ratio of 62:38.
- the soft segment was constructed by aliphatic polyester and the hard segment was constructed by aromatic crystal polyester.
- the LH-TPE polymer having a shore hardness of 30D and a melting point of 150°C was melt spun to prepare a LH-TPE yarn (16.7tex /72F).
- the HH-TPE yarn and the LH-TPE yarn were crossed upon each other at a ratio of 1:1 to form a woven fabric similarly as Example 1. Subsequently, the woven fabric was preheated and hot-pressed as described in Example 1 to form a reinforced composite fabric of Example 3. Differently, the preheating temperature to the woven fabric was 150°C and the hot-pressing temperature to the woven fabric was 170°C.
- a HH-TPE polymer used in the instant example was thermoplastic olefinic elastomer (TPO), which had a soft segment and a hard segment at a ratio of 35:65.
- the soft segment was constructed by ethylene propylene diene monomer (EPDM) and the hard segment was constructed by polypropylene (PP).
- the HH-TPE polymer having a shore hardness of 75D and a melting point of 160°C was melt spun to prepare a HH-TPE yarn (16.7tex /72F).
- a LH-TPE polymer used in the instant example was TPO, which had a soft segment and a hard segment at a ratio of 68:32.
- the soft segment was constructed by EPDM and the hard segment was constructed by PP.
- the LH-TPE polymer having a shore hardness of 56A and a melting point of 70°C was melt spun to prepare a LH-TPE yarn (16.7tex /72F).
- the HH-TPE yarn and the LH-TPE yarn were crossed upon each other at a ratio of 1:1 to form a woven fabric similarly as in Example 1.
- the woven fabric was preheated and hot-pressed as described in Example 1 to form a reinforced composite fabric of Example 4. Differently, the preheating temperature to the woven fabric was 70°C and the hot-pressing temperature to the woven fabric was 100°C.
- a HH-TPE polymer used in the instant example similarly as in Example 1 was melt spun to prepare a HH-TPE fiber (8.3tex/36F).
- the HH-TPE fiber and a polyethylene terephthalate (PET) fiber (8.3tex/36F) were twisted to form a HH-TPE yarn (16.7tex /72F).
- a LH-TPE polymer similarly as in Example 1 was melt spun to prepare a LH-TPE yarn (16.7tex /72F).
- Example 5 The HH-TPE yarn and the LH-TPE yarn were crossed upon each other at a ratio of 1:1 to form a woven fabric similarly as in Example 1. Subsequently, the woven fabric was preheated and hot-pressed as described in Example 1 to form a reinforced composite fabric of Example 5.
- a HH-TPE yarn (16.7tex /72F) and a LH-TPE yarn (16.7tex /72F) used in the instant example were similar to those in Example 1. Differently, the HH-TPE yarn and the LH-TPE yarn were knitted at a ratio of 1:1 to form a knitted fabric. Subsequently, the knitted fabric was preheated and hot-pressed as described in Example 1 to form a reinforced composite fabric of Example 6.
- a HH-TPE yarn (16.7tex /72F) and a LH-TPE yarn (16.7tex /72F) used in the instant example were similar to those in Example 5. Differently, the HH-TPE yarn and the LH-TPE yarn were knitted at a ratio of 1:1 to form a knitted fabric. Subsequently, the knitted fabric was preheated and hot-pressed as described in Example 5 to form a reinforced composite fabric of Example 7.
- a HH-TPE yarn (16.7tex /72F) used in the instant example was similar to that in Example 1.
- a LH-TPE yarn (16.7tex /72F) used in the instant example was similar to that in Example 4. Besides, the HH-TPE yarn and the LH-TPE yarn were crossed upon each other at a ratio of 1:1 to form a woven fabric.
- Example 8 the woven fabric was preheated and hot-pressed as described in Example 4 to form a reinforced composite fabric of Example 8.
- a HH-TPE polymer used in the instant comparative example similarly as in Example 1 was melt spun to prepare two identical HH-TPE yarns (16.7tex /72F). The two HH-TPE yarns were crossed upon each other to form a woven fabric similarly as in Example 1.
- the woven fabric was preheated and hot-pressed as described in Example 1.
- a woven fabric used in the instant comparative example was similar to that in Comparative Example 1.
- the woven fabric was preheated and hot-pressed as described in Example 1. Differently, the preheating temperature to the woven fabric was 190°C and the hot-pressing temperature to the woven fabric was 230°C.
- the two HH-TPE yarns were melted and formed into a piece of TPU polymer film.
- the piece of TPU polymer no longer had a texture of the woven fabric.
- the tensile strength of the fabric and the tensile strength of the reinforced composite fabric were measured according to ASTM-D142 specified by American Society for Testing and Materials (ASTM). Also, the impact strength of the fabric and the impact strength of the reinforced composite fabric were measured according to ASTM-D256 specified by ASTM.
- Table 1 the type of the HH-TPE polymers, the ratios of the soft segment to the hard segment (abbreviated as SS:HS) of the HH-TPE polymers, the shore hardness of the HH-TPE polymers, and the melting points of the HH-TPE polymers in Examples 1 to 8 (abbreviated as E1 to E8) and the type of the LH-TPE polymers, the SS:HS ratios of the LH-TPE polymers, the shore hardness of the LH-TPE polymers, and the melting points (°C) of the LH-TPE polymers in Examples 1 to 8 (abbreviated as E1 to E8).
- HH-TPE polymer LH-TPE polymer Type SS HS Hardness Melting point
- Type SS HS Hardness Melting point
- Table 2 the ratios of the HH-TPE yarn to the LH-TPE yarn (abbreviated as HH-yarn:LH-yarn) of the fabrics,
- the HH-/LH-TPE yarns can be prepared by the HH-/LH-TPE polymers with different hardness or different melting points by controlling the SS:HS ratios of the HH-/LH-TPE polymers.
- the tensile strengths and the impact strengths of the reinforced composite fabrics in Examples 1 to 8 were higher than those of the fabrics in Examples 1 to 8. Therefore, the present invention could prepare the reinforced composite fabrics with higher tensile strength and higher impact strength.
- the HH-TPE polymer and the LH-TPE polymer were classified as identical thermoplastic elastomeric polymer in Examples 1 to 7.
- the LH-TPE polymer and the HH-TPE polymer in Examples 1, 2, 5, and 8 were TPU.
- the SS:HS ratios of the LH-TPE polymer ranged from 56:44 to 70:30
- the shore hardness of the LH-TPE yarn ranged from 10A to 90A
- the melting points of the LH-TPE yarn ranged from 50°C to 150°C.
- the SS:HS ratios of the HH-TPE polymer ranged from 30:70 to 50:50
- the shore hardness of the HH-TPE yarn ranged from 95A to 90D and the melting points of the HH-TPE yarn ranged from 170°C to 300°C.
- the LH-TPE polymer and the HH-TPE polymer in Example 3 were TPEE.
- the SS:HS ratio of the LH-TPE polymer ranged from 52:48 to 75:25
- the shore hardness of the LH-TPE yarn ranged from 30D to 60D
- the melting point of the LH-TPE yarn ranged from 100°C to 180°C.
- the SS:HS ratio of the HH-TPE polymer ranged from 30:70 to 40:60
- the shore hardness of the HH-TPE yarn ranged from 65D to 80D and the melting points of the HH-TPE yarn ranged from 185°C to 280°C.
- the LH-TPE polymer and the HH-TPE polymer in Examples 4 and 8 were TPO.
- the SS:HS ratios of the LH-TPE polymer ranged from 55:45 to 75:25
- the shore hardness of the LH-TPE yarn ranged from 30A to 60A and the melting point of the LH-TPE yarn ranged from 50°C to 80°C.
- the SS:HS ratios of the HH-TPE polymer ranged from 30:70 to 40:60
- the shore hardness of the HH-TPE yarn ranged from 65A to 90A and the melting point of the HH-TPE yarn ranged from 100°C to 180°C.
- the HH-TPE polymers in Examples 1 and 8 were both TPU. Differently, the LH-TPE polymer in Example 1 was TPU but the LH-TPE polymer in Example 8 was TPO. With reference to Table 2, the tensile strength and the impact strength of the reinforced composite fabric in Example 1 were higher than those in Example 8 due to the higher affinity between the HH-TPE yarn and the LH-TPE yarn.
- the LH-TPE polymers in Examples 4 and 8 were both TPO.
- the HH-TPE polymer in Example 4 was TPO but the HH-TPE polymer in Example 8 was TPU.
- the tensile strength of the reinforced composite fabric in Example 8 was higher than that in Example 4.
- the impact strength of the reinforced composite fabric in Example 4 was higher than that in Example 8. Therefore, the reinforced composite fabric prepared by various types of HH-TPE polymers or by various types of LH-TPE polymers would have different characteristics of mechanical strengths.
- the PET fiber and the TPU fiber were twisted to form the HH-TPE yarn in Examples 5 and 7.
- the tensile strengths and the impact strengths of the reinforced composite fabrics in Examples 5 and 7 were increased.
- the tensile strength of the reinforced composite fabric in Example 5 was 52MPa; the impact strength of the reinforced composite fabric in Example 5 was 287 J/m.
- the tensile strength of the reinforced composite fabric in Example 7 was 26.2MPa; the impact strength of the reinforced composite fabric in Example 7 was 148 J/m.
- Examples 1 and 6 were respectively prepared similarly. That is, the difference between the first group and the second group was only the types of the fabrics.
- the tensile strength and the impact strength of the reinforced composite fabric made by woven fabrics were higher than those of the reinforced composite fabric made by knitted fabrics (Examples 6 and 7).
- Comparing Example 1 with Comparative Example 1 the woven fabric in Comparative Example 1 was woven by two identical HH-TPE yarns. After preheating and hot-pressing the woven fabric, the woven fabric did not form the reinforced composite fabric. With reference to Table 2, the tensile strength and the impact strength of the reinforced composite fabric in Comparative Example 1 did not increase obviously.
- Comparing Example 1 with Comparative Example 2 the woven fabric in Comparative Example 2 was woven by two identical HH-TPE yarns and the hot-pressing temperature was not higher than or equal to the melting point of the HH-TPE yarn. From the result, the woven fabric in the Comparative Example 2 not only could not form the reinforced composite fabric but also would lose the texture of the fabric. Therefore, using the HH-TPE yarn and the LH-TPE yarn and controlling the hot-pressing temperature to the fabrics in a specific range are important features to prepare the reinforced composite fabrics.
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Claims (17)
- Procédé de fabrication d'un tissu composite renforcé, caractérisé en ce que ce procédé comprend les étapes qui consistent en :la formation d'un fil élastomère thermoplastique à haute dureté (2) et un fil élastomère thermoplastique à basse dureté (3) en un tissu par tissage ; une température de fusion du fil élastomère thermoplastique à basse dureté (3) allant de 50°C à 150 ; une dureté shore du fil élastomère thermoplastique à basse dureté (3) allant de 10A à 90A et une dureté shore du fil élastomère thermoplastique à haute dureté (2) allant de 95A à 90D ;le pressage à chaud du tissu à une température de pressage à chaud et une pression de pressage à chaud pour la formation du tissu composite renforcé ; la température de pressage à chaud étant supérieure ou égale à la température de fusion du fil élastomère thermoplastique à basse dureté (3), et inférieure à une température de fusion du fil élastomère thermoplastique à haute dureté (2).
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 1, où la température de pressage à chaud est supérieure à la température de fusion du fil élastomère thermoplastique à basse dureté (3) de 10°C à 50°C.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 1, où la température de fusion du fil élastomère thermoplastique à haute dureté (2) est entre 150°C et 300°C.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 1, où le procédé comprend la torsion d'une fibre élastomère thermoplastique à haute dureté et une fibre de renforcement dans le fil élastomère thermoplastique à haute dureté (2).
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 4, où la fibre de renforcement comprend une fibre de carbone, une fibre de verre, une fibre de Kevlar ou une fibre Dyneema; un pourcentage de la fibre de renforcement va de 10% en poids à 90% en poids basé sur le poids total du fil élastomère thermoplastique à haute dureté (2).
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 1, où le procédé comprend :la trempe sur roue d'un polymère élastomère thermoplastique à haute dureté dans le fil élastomère thermoplastique à haute dureté (2); etla trempe sur roue d'un polymère élastomère thermoplastique à basse dureté dans le fil élastomère thermoplastique à basse dureté (3); oùle polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté sont indépendamment : élastomère en caoutchouc thermoplastique, élastomère en polyuréthane thermoplastique, élastomère thermoplastique à base de styrène, élastomère oléfinique thermoplastique, élastomère vulcanisé thermoplastique, élastomère en ester thermoplastique ou élastomère en polyamide thermoplastique.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 2, où le procédé comprend :la trempe sur roue d'un polymère élastomère thermoplastique à haute dureté dans le fil élastomère thermoplastique à haute dureté (2); etla trempe sur roue d'un polymère élastomère thermoplastique à basse dureté dans le fil élastomère thermoplastique à basse dureté (3); oùle polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté sont indépendamment : élastomère en caoutchouc thermoplastique, élastomère en polyuréthane thermoplastique, élastomère thermoplastique à base de styrène, élastomère oléfinique thermoplastique, élastomère vulcanisé thermoplastique, élastomère en ester thermoplastique ou élastomère en polyamide thermoplastique.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 3, où le procédé comprend :la trempe sur roue d'un polymère élastomère thermoplastique à haute dureté dans le fil élastomère thermoplastique à haute dureté (2); etla trempe sur roue d'un polymère élastomère thermoplastique à basse dureté dans le fil élastomère thermoplastique à basse dureté (3); oùle polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté sont indépendamment: élastomère en caoutchouc thermoplastique, élastomère en polyuréthane thermoplastique, élastomère thermoplastique à base de styrène, élastomère oléfinique thermoplastique, élastomère vulcanisé thermoplastique, élastomère en ester thermoplastique ou élastomère en polyamide thermoplastique.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 6, où le polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté sont classifiés comme polymères élastomères thermoplastiques identiques.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 6, où le polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté ont respectivement chacun un segment souple et un segment rigide, une proportion du segment souple par rapport au segment rigide du polymère élastomère thermoplastique à haute dureté va de 25:75 à 50:50 ; une proportion du segment souple par rapport au segment rigide du polymère élastomère à basse dureté va de 51:49 à 80:20.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 6, où le polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté sont tous deux classifiés comme polymères élastomères thermoplastiques ; le polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté ont respectivement chacun un segment souple et un segment rigide ; une proportion du segment souple par rapport au segment rigide du polymère élastomère thermoplastique à haute dureté va de 30:70 à 50:50, une proportion du segment souple par rapport au segment rigide du polymère élastomère thermoplastique à basse dureté va de 56:44 à 70:30.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 6, où le polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté sont tous deux classifiés comme élastomères en ester polyéther thermoplastique ; le polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté ont respectivement chacun un segment souple et un segment rigide ; une proportion du segment souple par rapport au segment rigide du polymère élastomère thermoplastique à haute dureté va de 30:70 à 40:60 ; une proportion du segment souple par rapport au segment rigide du polymère élastomère thermoplastique à basse dureté va de 52:48 à 75:25.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 6, où le polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté sont tous deux classifiés comme élastomères oléfiniques thermoplastiques; le polymère élastomère thermoplastique à haute dureté et le polymère élastomère thermoplastique à basse dureté ont respectivement chacun un segment souple et un segment rigide ; une proportion du segment souple par rapport au segment rigide du polymère élastomère thermoplastique à haute dureté va de 30:70 à 40:60 ; une proportion du segment souple par rapport au segment rigide du polymère élastomère thermoplastique à basse dureté va de 55:45 à 75:25.
- Procédé de fabrication du tissu composite renforcé comme revendiqué dans la revendication 1, où l'étape de la formation d'un fil élastomère thermoplastique à haute dureté (2) et d'un fil élastomère thermoplastique à basse dureté (3) en un tissu par le tissage comprend en outre la torsion du fil élastomère thermoplastique à haute dureté (2) et du fil élastomère thermoplastique à basse dureté (3) en une multitude de fils complexes et le tissage de la multitude de fils complexes en tissu, chacun des fils complexes comprend le fil élastomère thermoplastique à haute dureté (2) et le fil élastomère thermoplastique à basse dureté (3) précités torsadés ensemble.
- Tissu composite renforcé tissé, caractérisé où tissu composite renforcé comprend :
un fil élastomère thermoplastique à haute dureté (2) et un fil élastomère thermoplastique à basse dureté (3), une partie d'une surface du fil élastomère thermoplastique à basse dureté (3) étant fondue et attachée sur une surface du fil élastomère thermoplastique à haute dureté (2) ; une dureté shore du fil élastomère thermoplastique à basse dureté (3) allant de 10A à 90A et une dureté shore du fil élastomère thermoplastique à haute dureté (2) allant de 95A à 90D. - Tissu composite renforcé comme revendiqué dans la revendication 15, où le fil élastomère thermoplastique à haute dureté (2) est torsadé à partir d'une fibre élastomère thermoplastique à haute dureté et d'une fibre de renforcement.
- Tissu composite renforcé comme revendiqué dans la revendication 15, où le tissu composite renforcé est tissé à partir d'une multitude de fils complexes, chacun des fils complexes comprenant le fil élastomère thermoplastique à haute dureté (2) et le fil élastomère thermoplastique à basse dureté (3) précités torsadés ensemble.
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ES17152774T ES2762073T3 (es) | 2017-01-24 | 2017-01-24 | Tejido compuesto reforzado y su proceso de fabricación |
EP17152774.0A EP3266914B1 (fr) | 2017-01-24 | 2017-01-24 | Tissu composite renforcé et son procédé de fabrication |
PL17152774T PL3266914T3 (pl) | 2017-01-24 | 2017-01-24 | Wzmocniona tkanina kompozytowa i sposób jej wytwarzania |
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DE19537703A1 (de) * | 1995-10-11 | 1997-04-17 | Hoechst Trevira Gmbh & Co Kg | Textile Flächengebilde hoher Dichte aus Polyesterhybridgarnen, Verfahren zur Herstellung von Verbundwerkstoffen und Verwendung der textilen Flächengebilde |
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