JP5060621B2 - Automotive interior materials - Google Patents
Automotive interior materials Download PDFInfo
- Publication number
- JP5060621B2 JP5060621B2 JP2010533365A JP2010533365A JP5060621B2 JP 5060621 B2 JP5060621 B2 JP 5060621B2 JP 2010533365 A JP2010533365 A JP 2010533365A JP 2010533365 A JP2010533365 A JP 2010533365A JP 5060621 B2 JP5060621 B2 JP 5060621B2
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- JP
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- Prior art keywords
- resin
- fiber
- paper
- breathable
- fibers
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 241001416177 Vicugna pacos Species 0.000 description 1
- 241000282840 Vicugna vicugna Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical compound [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229920006221 acetate fiber Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000004018 acid anhydride group Chemical group 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
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- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
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- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
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- 239000001099 ammonium carbonate Substances 0.000 description 1
- 210000000077 angora Anatomy 0.000 description 1
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- 239000004760 aramid Substances 0.000 description 1
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- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
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- 229910052796 boron Inorganic materials 0.000 description 1
- 150000001639 boron compounds Chemical class 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
- OHDKESUYWHDEOQ-UHFFFAOYSA-N butanoyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(=O)CCC OHDKESUYWHDEOQ-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
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- 239000000378 calcium silicate Substances 0.000 description 1
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- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical compound [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 description 1
- 235000010261 calcium sulphite Nutrition 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
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- 235000005822 corn Nutrition 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- PVAONLSZTBKFKM-UHFFFAOYSA-N diphenylmethanediol Chemical class C=1C=CC=CC=1C(O)(O)C1=CC=CC=C1 PVAONLSZTBKFKM-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229920006248 expandable polystyrene Polymers 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 229920006283 heat-resistant synthetic fiber Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
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- 210000000050 mohair Anatomy 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000004058 oil shale Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000002984 plastic foam Substances 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920005594 polymer fiber Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920006327 polystyrene foam Polymers 0.000 description 1
- 229920006306 polyurethane fiber Polymers 0.000 description 1
- 239000011496 polyurethane foam Substances 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 229920006345 thermoplastic polyamide Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 238000009732 tufting Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60N—SEATS SPECIALLY ADAPTED FOR VEHICLES; VEHICLE PASSENGER ACCOMMODATION NOT OTHERWISE PROVIDED FOR
- B60N3/00—Arrangements or adaptations of other passenger fittings, not otherwise provided for
- B60N3/04—Arrangements or adaptations of other passenger fittings, not otherwise provided for of floor mats or carpets
- B60N3/048—Arrangements or adaptations of other passenger fittings, not otherwise provided for of floor mats or carpets characterised by their structure
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R13/00—Elements for body-finishing, identifying, or decorating; Arrangements or adaptations for advertising purposes
- B60R13/08—Insulating elements, e.g. for sound insulation
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Transportation (AREA)
- Physics & Mathematics (AREA)
- Acoustics & Sound (AREA)
- Laminated Bodies (AREA)
- Vehicle Interior And Exterior Ornaments, Soundproofing, And Insulation (AREA)
- Paper (AREA)
- Soundproofing, Sound Blocking, And Sound Damping (AREA)
- Passenger Equipment (AREA)
Description
本発明は主として床敷用に供される自動車用内装材に関するものである。 The present invention relates to an automobile interior material mainly used for flooring.
この種の自動車用内装材としては、一般に所定の通気抵抗を有する通気性材料が使用される。例えば特許文献1には目付が150〜800g/m2、嵩密度が0.01〜0.2g/cm3である不織布と、JIS L−1096に基づいて測定される通気量が50cc/cm2/sec以下の表皮材とを積層した吸音材が記載され、特許文献2には目付けが150〜800g/m2、嵩密度が0.01〜0.2g/m3の不織布を表皮材として積層した易成形性吸音材が記載され、特許文献3には、空気流に対しての総抵抗Rt=500Nsm−3〜Rt=2500Nsm−3を有するファイバー層またはファイバー/フォーム複合体層を備えた遮音キットが記載されている。
上記吸音材あるいは遮音キットは、内部に侵入した音のエネルギーを摩擦エネルギーに変えて吸収するものである。
更に上記吸音材の吸音性能を高めるために、上記各吸音材に使用されている通気性材料に加え、更に多数の貫通孔を設けたゴム層あるいは樹脂層を挿入した構成のものが提案されている。
例えば特許文献4には、フロアマットの裏面に複数の貫通孔を設けたゴム層を裏打ちした吸音材層を積層した構成が記載され、特許文献5には、保形フェルト層の上側に開孔樹脂層を積層し、下側に非通気樹脂シートを積層することによって該開孔樹脂層から該保形フェルト層内に侵入した音波を該開孔樹脂層と該非通気樹脂シート間に閉じ込めて該保形フェルト内で乱反射させ、音のエネルギーを高い効率で吸収する内装材が記載されている。
As this type of automobile interior material, a breathable material having a predetermined ventilation resistance is generally used. For example, Patent Document 1 discloses a nonwoven fabric having a basis weight of 150 to 800 g / m 2 and a bulk density of 0.01 to 0.2 g / cm 3 , and an air flow rate measured based on JIS L-1096 of 50 cc / cm 2. A sound-absorbing material laminated with a skin material of / sec or less is described, and Patent Document 2 laminates a nonwoven fabric having a basis weight of 150 to 800 g / m 2 and a bulk density of 0.01 to 0.2 g / m 3 as a skin material. And a fiber / foam composite layer having a total resistance to air flow R t = 500 Nsm −3 to R t = 2500 Nsm −3. A sound insulation kit is described.
The sound-absorbing material or the sound-insulating kit absorbs the energy of sound that has entered the inside by converting it into frictional energy.
Furthermore, in order to enhance the sound absorbing performance of the sound absorbing material, a structure in which a rubber layer or a resin layer provided with a number of through holes is inserted in addition to the breathable material used in each of the sound absorbing materials has been proposed. Yes.
For example, Patent Document 4 describes a structure in which a sound absorbing material layer lined with a rubber layer provided with a plurality of through holes is laminated on the back surface of a floor mat, and Patent Document 5 discloses an opening above the shape retaining felt layer. By laminating a resin layer and laminating a non-breathable resin sheet on the lower side, the sound waves that have entered the shape-retaining felt layer from the perforated resin layer are confined between the perforated resin layer and the non-breathable resin sheet. It describes an interior material that diffusely reflects in a shape-retaining felt and absorbs sound energy with high efficiency.
上記ゴム層あるいは樹脂層を挿入する構成とする場合、これらに貫通孔を設ける加工方法には、一般的に針刺し加工が適用される。ところが、針刺し加工によって設けられる貫通孔の径は針の太さによって決まるため、径が微小な貫通孔、特に直径0.1mm以下の微小貫通孔を設けることは殆んど不可能であるという問題点がある。また樹脂層やゴム層が有する弾性復元力により、貫通孔を形成しても該貫通孔が塞がってしまうという問題点もある。 When the rubber layer or the resin layer is configured to be inserted, needle stick processing is generally applied to a processing method for providing a through hole in the rubber layer or the resin layer. However, since the diameter of the through hole provided by the needle piercing process is determined by the thickness of the needle, there is a problem that it is almost impossible to provide a through hole with a minute diameter, particularly a minute through hole with a diameter of 0.1 mm or less. There is a point. Further, there is a problem that even if the through hole is formed, the through hole is blocked by the elastic restoring force of the resin layer or the rubber layer.
本発明は上記従来の課題を解決するための手段として、多孔質マット5上に非通気性樹脂シート4が積層され、該非通気性樹脂シート4上に成形性フェルト3が積層され、該成形性フェルト3上に、紙材料1を裏打ちした通気性表装材2が積層された自動車用内装材6であって、上記紙材料1は叩解度がJIS P 8121−1995の4.カナディアン・スタンダード・フリーネスに規定されるカナダ標準型ろ水度で350〜650ml(CSF)の範囲であり表面に開口する多数の細孔が設けられている多孔質パルプ繊維を90質量%以上含み、通気抵抗が0.07〜3.00kPa・s/mの範囲の紙であることを特徴とする自動車用内装材6を提供するものである。
上記紙材料1は表面に多数の凹凸を形成することによって延伸性を付与されたクレープ加工および/またはエンボス加工紙であることが望ましく、上記紙材料1の目付量は15g/m2〜50g/m2であることが望ましい。
また、上記成形性フェルト3の目付量は50〜1000g/m2であり、厚さが1.5mm以上であり、融点が180℃以下の低融点熱可塑性樹脂繊維を10〜50質量%含有し、通気抵抗が0.04〜1.50kPa・s/mであることが望ましい。
In the present invention, as a means for solving the above-described conventional problems, a non-breathable resin sheet 4 is laminated on a porous mat 5, and a moldable felt 3 is laminated on the non-breathable resin sheet 4. An automotive interior material 6 in which a breathable outer covering material 2 lined with a paper material 1 is laminated on a felt 3, wherein the paper material 1 has a beating degree of JIS P 8121-1995. 90% by mass or more of a porous pulp fiber having a Canadian standard freeness prescribed by Canadian Standard Freeness in the range of 350 to 650 ml (CSF) and having a large number of pores opened on the surface, The present invention provides an automobile interior material 6 characterized in that it is a paper having a ventilation resistance of 0.07 to 3.00 kPa · s / m.
The paper material 1 is desirably a crepe and / or embossed paper imparted with stretchability by forming a large number of irregularities on the surface, and the basis weight of the paper material 1 is 15 g / m 2 to 50 g / m 2 is desirable.
The moldable felt 3 has a basis weight of 50 to 1000 g / m 2 , a thickness of 1.5 mm or more, and a low melting point thermoplastic resin fiber having a melting point of 180 ° C. or less and containing 10 to 50% by mass. The airflow resistance is preferably 0.04 to 1.50 kPa · s / m.
〔作用〕
本発明では、形成可能な貫通孔の最小径に限界があるゴム層や樹脂層を使わずに、叩解度がJIS P 8121−1995の4.カナディアン・スタンダード・フリーネスに規定されるカナダ標準型ろ水度で350〜650ml(CSF)の範囲であり表面に開口する多数の細孔が設けられている多孔質パルプ繊維を90質量%以上含み、通気抵抗が0.07〜3.00kPa・s/mの範囲に設定された紙材料1を使用して吸音性能を高めることを特徴とする。
上記紙材料1にあっては、繊維間の空隙に加えて繊維自体にも空隙が形成されているから、該紙材料1の繊維間の空隙および繊維自体の空隙に音が取り込まれて該音波が繊維を振動させることで、音のエネルギーを紙材料1内部で繊維同士が摩擦エネルギーとして吸収することにより、音のエネルギーを減衰する。
更には該多孔質パルプ繊維の表面には多数のケバが存在するため、該ケバもまた音によって振動することにより音のエネルギーを摩擦エネルギーとして吸収する。
該繊維の叩解度がろ水度で650ml(CSF)を超えている場合には、パルプ繊維のケバや同心円状の緩みが不充分となり、パルプ繊維表面に開口する多数の細孔による多孔質化が不充分となり空隙率が低下して内装材6の吸音性能に悪影響が及ぼされる。一方350ml(CSF)を下回るとパルプ繊維がフィブリル化することで細分化されてしまい、極微細繊維が増加するので、紙材料1の密度が高くなり、通気抵抗が高くなって、やはり内装材6の吸音特性に悪影響が及ぼされる。
[Action]
In the present invention, the beating degree is 4 of JIS P 8121-1995 without using a rubber layer or a resin layer that has a limit on the minimum diameter of the through-hole that can be formed. 90% by mass or more of a porous pulp fiber having a Canadian standard freeness prescribed by Canadian Standard Freeness in the range of 350 to 650 ml (CSF) and having a large number of pores opened on the surface, The sound absorbing performance is enhanced by using the paper material 1 having a ventilation resistance set in a range of 0.07 to 3.00 kPa · s / m.
In the paper material 1, since voids are formed in the fibers themselves in addition to the gaps between the fibers, sound is taken into the gaps between the fibers of the paper material 1 and the fibers themselves. When the fiber vibrates, the sound energy is attenuated as the friction energy is absorbed between the fibers in the paper material 1 inside the paper material 1.
Furthermore, since there are a large number of cracks on the surface of the porous pulp fiber, the cracks also absorb sound energy as frictional energy by vibrating with sound.
When the freeness of the fiber exceeds 650 ml (CSF) in terms of freeness, the pulp fiber is not sufficiently crushed or concentrically loosened and becomes porous due to a large number of pores opening on the surface of the pulp fiber. Becomes insufficient, the porosity is lowered, and the sound absorbing performance of the interior material 6 is adversely affected. On the other hand, if it is less than 350 ml (CSF), the pulp fibers are fragmented by fibrillation and the number of ultrafine fibers increases, so that the density of the paper material 1 is increased and the ventilation resistance is increased. Adversely affects the sound absorption characteristics.
このように本発明の内装材6にあっては、音が成形性フェルト3内に達するまでにすでに紙材料1によってエネルギーを大幅に吸収されており、更に音は該成形性フェルト3内で該紙材料1と該非通気性樹脂シート4とによって閉じ込められ、乱反射することによって効率良く吸収される。
また、パルプ繊維自体に多数の細孔が設けられることにより、通気層が全表面に渡り分布し、従来の樹脂層やゴム層のような所定部位にのみ貫通孔を設けたものと比べて吸音性に優れ、全体としての軽量化を図ることが出来、更に安価である。
As described above, in the interior material 6 of the present invention, the energy has already been greatly absorbed by the paper material 1 before the sound reaches the moldable felt 3, and the sound is further absorbed in the moldable felt 3. It is confined by the paper material 1 and the non-breathable resin sheet 4 and efficiently absorbed by irregular reflection.
In addition, a large number of pores are provided in the pulp fiber itself, so that the air-permeable layer is distributed over the entire surface, and the sound absorption is lower than that in which through holes are provided only at predetermined sites such as conventional resin layers and rubber layers. It is excellent in performance, can be reduced in weight as a whole, and is inexpensive.
〔効果〕
本発明の内装材6は極めて優れた吸音性能を有し、軽量でかつ安価な自動車用内装材6が提供される。そして該内装材6に使用する紙材料1は木質のパルプ繊維からなり、有機合成繊維のように製造工程で多量の炭酸ガスを発生せず、また腐朽性があり、更にまたバイオマスエネルギー(例えばバイオエタノールの原料)としても使用できるので、省エネルギー対策、地球温暖化防止対策にも資する材料である。
〔effect〕
The interior material 6 of the present invention has an extremely excellent sound absorbing performance, and a lightweight and inexpensive interior material 6 for an automobile is provided. The paper material 1 used for the interior material 6 is made of woody pulp fiber, does not generate a large amount of carbon dioxide gas in the production process like organic synthetic fiber, is decayable, and also has biomass energy (for example, bio-energy). Since it can also be used as a raw material for ethanol, it is also a material that contributes to energy saving measures and global warming prevention measures.
本発明の自動車用内装材6は例えば図3に示すように、下層から順に多孔質マット5、非通気性樹脂シート4、成形性フェルト3、紙材料1、通気性表装材2を積層したものである。
以下に各材料について詳説する。
For example, as shown in FIG. 3, the automobile interior material 6 of the present invention is a laminate in which a porous mat 5, a non-breathable resin sheet 4, a moldable felt 3, a paper material 1, and a breathable surface covering material 2 are laminated in order from the lower layer. It is.
Each material is described in detail below.
〔多孔質マット〕
多孔質マット5は上記内装材6に好適なクッション性を付与すると共に、非通気性樹脂シート4を自動車内の壁面や床面等から一定距離を保つことによって、該内装材6に良好な遮音効果を付するものである。
上記多孔質マット5としては、例えば後述する通気性表装材2や成形性フェルト3に用いられる繊維シートやマットが使用される。
また、上記多孔質マット5の材料としては、通気性ポリウレタン発泡体、通気性ポリエチレン発泡体、通気性ポリプロピレン発泡体、通気性ポリスチレン発泡体、通気性フェノール樹脂発泡体、通気性メラミン樹脂発泡体等の通気性プラスチック発泡体からなるシートまたはマットが用いられてもよい。
上記内装材6に良好なクッション性や遮音効果を付与するために、多孔質マット5の目付量は50〜1000g/m2であることが望ましく、厚みは5〜30mmであることが望ましい。
[Porous mat]
The porous mat 5 imparts a suitable cushioning property to the interior material 6 and keeps the air-impermeable resin sheet 4 at a certain distance from the wall surface, floor surface, etc. in the automobile, thereby providing good sound insulation to the interior material 6. It is an effect.
As the porous mat 5, for example, a fiber sheet or a mat used for a breathable outer covering material 2 or a moldable felt 3 described later is used.
Examples of the material of the porous mat 5 include breathable polyurethane foam, breathable polyethylene foam, breathable polypropylene foam, breathable polystyrene foam, breathable phenolic resin foam, and breathable melamine resin foam. A sheet or mat made of a breathable plastic foam may be used.
In order to give a good cushioning and sound insulation effect to the interior material 6, the basis weight of the porous mat 5 is desirably 50 to 1000 g / m 2 and the thickness is desirably 5 to 30 mm.
〔非通気性樹脂シート〕
非通気性樹脂シート4は、例えばポリエチレン、ポリプロピレン、エチレン−プロピレン共重合体、エチレン−酢酸ビニル共重合体、ポリ塩化ビニル、ポリ塩化ビニリデン、ポリスチレン、ポリ酢酸ビニル、フッ素樹脂、熱可塑性アクリル樹脂、熱可塑性ポリエステル、熱可塑性ポリアミド、熱可塑性ウレタン樹脂、アクリロニトリル−ブタジエン共重合体、スチレン−ブタジエン共重合体、アクリロニトリル−ブタジエン−スチレン共重合体、エチレン−プロピレン共重合体、エチレン−プロピレンターポリマー、エチレン−酢酸ビニル共重合体等の熱可塑性樹脂のシートである。
該非通気性樹脂シート4には、必要に応じてタルク、炭酸カルシウム等の充填剤や顔料等の着色剤等を添加してもよい。
上記非通気性樹脂シート4は該内装材6に良好な遮音性能を寄与するものであり、また該内装材6を所定形状に成形する際には成形形状を安定化させるものである。
上記非通気性樹脂シート4は良好な遮音性能を発揮するという観点から、目付量は20〜1000g/m2であることが望ましく、厚みは0.01〜3.0mmであることが望ましい。
[Non-breathable resin sheet]
Non-breathable resin sheet 4 is, for example, polyethylene, polypropylene, ethylene-propylene copolymer, ethylene-vinyl acetate copolymer, polyvinyl chloride, polyvinylidene chloride, polystyrene, polyvinyl acetate, fluororesin, thermoplastic acrylic resin, Thermoplastic polyester, thermoplastic polyamide, thermoplastic urethane resin, acrylonitrile-butadiene copolymer, styrene-butadiene copolymer, acrylonitrile-butadiene-styrene copolymer, ethylene-propylene copolymer, ethylene-propylene terpolymer, ethylene -A sheet of thermoplastic resin such as vinyl acetate copolymer.
If necessary, the non-breathable resin sheet 4 may be added with a filler such as talc and calcium carbonate, or a colorant such as a pigment.
The non-breathable resin sheet 4 contributes good sound insulation performance to the interior material 6 and stabilizes the molded shape when the interior material 6 is molded into a predetermined shape.
The non-breathable resin sheet 4 desirably has a basis weight of 20 to 1000 g / m 2 and a thickness of 0.01 to 3.0 mm from the viewpoint of exhibiting good sound insulation performance.
〔成形性フェルト〕
成形性フェルト3としては、繊維にバインダーとして熱硬化性樹脂初期縮合物を混合して、所望なれば該初期縮合物をB状態にした熱硬化性フェルト、繊維にバインダーとして擬似熱可塑性樹脂を混合した擬似熱可塑性フェルト、繊維にバインダーとして熱可塑性樹脂および/または低融点熱可塑性樹脂繊維を混合した熱可塑性フェルトがある。
上記熱硬化性フェルトや上記擬似熱可塑性フェルトや上記熱可塑性フェルトである成形性フェルト3に使用される繊維としては、例えば、ポリエステル繊維、ポリアミド繊維、アクリル繊維、ウレタン繊維、ポリ塩化ビニル繊維、ポリ塩化ビニリデン繊維、アセテート繊維等の合成繊維、羊毛、モヘア、カシミア、ラクダ毛、アルパカ、ビキュナ、アンゴラ、蚕糸、キワタ、ガマ繊維、パルプ、木綿、ヤシ繊維、麻繊維、竹繊維、ケナフ繊維等の天然繊維、デンプン系、ポリ乳酸系等の生分解性繊維、レーヨン(人絹、スフ)、ポリノジック、キュプラ、アセテート、トリアセテート等のセルロース系人造繊維、ガラス繊維、炭素繊維、セラミック繊維、石綿繊維等の無機繊維、これらの繊維を使用した繊維製品のスクラップを解繊して得られた再生繊維等である。これらの繊維は、単独あるいは2種以上組合わせて使用される。
[Molding felt]
As the moldable felt 3, a thermosetting resin initial condensate is mixed with the fiber as a binder, and if desired, a thermosetting felt in which the initial condensate is in a B state, and a pseudo thermoplastic resin is mixed with the fiber as a binder. Pseudo thermoplastic felt, and thermoplastic felt in which a thermoplastic resin and / or a low melting point thermoplastic resin fiber is mixed as a binder with the fiber.
Examples of fibers used for the thermosetting felt, the pseudo thermoplastic felt, and the moldable felt 3 that is the thermoplastic felt include polyester fiber, polyamide fiber, acrylic fiber, urethane fiber, polyvinyl chloride fiber, poly Synthetic fibers such as vinylidene chloride fiber and acetate fiber, wool, mohair, cashmere, camel hair, alpaca, vicuña, angora, silk thread, kiwata, gama fiber, pulp, cotton, palm fiber, hemp fiber, bamboo fiber, kenaf fiber, etc. Natural fiber, starch-based, polylactic acid-based biodegradable fiber, rayon (man-made silk, sufu), polynosic, cupra, acetate, triacetate and other cellulosic artificial fibers, glass fiber, carbon fiber, ceramic fiber, asbestos fiber, etc. Obtained by defibrating scraps of inorganic fibers and fiber products using these fibers It was a recycled fiber and the like. These fibers are used alone or in combination of two or more.
上記熱硬化性フェルトに使用される熱硬化性樹脂としては、例えばウレタン系樹脂、メラミン系樹脂、熱硬化型アクリル系樹脂、特に加熱によりエステル結合を形成して硬化する熱硬化性アクリル系樹脂、尿素系樹脂、フェノール系樹脂、エポキシ系樹脂、熱硬化型ポリエステル系樹脂等が使用されるが、該合成樹脂を生成するウレタン樹脂プレポリマー、尿素系樹脂プレポリマー(初期縮合体)、フェノール系樹脂プレポリマー(初期縮合体)、ジアリルフタレートプレポリマー、アクリルオリゴマー、多価イソシアナート、メタクリルエステルモノマー、ジアリルフタレートモノマー等のプレポリマー、オリゴマー、モノマー等の合成樹脂前駆体が使用されてもよい。該熱硬化性樹脂は取り扱いが容易な点から、水溶液、水性エマルジョン、水性ディスパーションの形のものを使用することが好ましいが、有機溶剤溶液の形のものを使用してもよい。 Examples of the thermosetting resin used in the thermosetting felt include a urethane resin, a melamine resin, a thermosetting acrylic resin, particularly a thermosetting acrylic resin that cures by forming an ester bond by heating, Urea resins, phenolic resins, epoxy resins, thermosetting polyester resins, etc. are used, but urethane resin prepolymers, urea resin prepolymers (initial condensates), phenolic resins that produce the synthetic resins Synthetic resin precursors such as prepolymers such as prepolymers (initial condensates), diallyl phthalate prepolymers, acrylic oligomers, polyvalent isocyanates, methacrylic ester monomers, diallyl phthalate monomers, oligomers, and monomers may be used. The thermosetting resin is preferably used in the form of an aqueous solution, an aqueous emulsion, or an aqueous dispersion because it is easy to handle, but may be used in the form of an organic solvent solution.
また、特に成形性フェルト3に使用される熱硬化性樹脂として望ましいのは、フェノール系樹脂である。該フェノール系樹脂は、フェノール系化合物とホルムアルデヒドおよび/またはホルムアルデヒド供与体とを縮合させることによって得られる。
上記フェノール系樹脂に使用されるフェノール系化合物としては、一価フェノールであってもよいし、多価フェノールであってもよいし、一価フェノールと多価フェノールとの混合物であってもよいが、一価フェノールのみを使用した場合、硬化時および硬化後にホルムアルデヒドが放出され易いため、好ましくは多価フェノールまたは一価フェノールと多価フェノールとの混合物を使用する。
上記熱硬化性樹脂あるいは合成樹脂前駆体は二種以上混合使用されてもよい。
Particularly desirable as a thermosetting resin used for the moldable felt 3 is a phenolic resin. The phenolic resin is obtained by condensing a phenolic compound with formaldehyde and / or a formaldehyde donor.
The phenolic compound used in the phenolic resin may be a monohydric phenol, a polyhydric phenol, or a mixture of a monohydric phenol and a polyhydric phenol. When only monohydric phenol is used, formaldehyde is easily released during and after curing. Therefore, polyhydric phenol or a mixture of monohydric phenol and polyhydric phenol is preferably used.
Two or more of the above thermosetting resins or synthetic resin precursors may be used in combination.
上記擬似熱可塑性フェルトに使用される擬似熱可塑性樹脂は、
(A)5〜100質量%がエチレン性不飽和酸無水物またはカルボン酸基が酸無水物基を形成することができるエチレン性不飽和ジカルボン酸からなるラジカル重合により得られたポリマーと、
(B)少なくとも2つのヒドロキシル基を有するアルカノールアミンと、
(A)+(B)の和に対して1.5質量%より少ない、リン含有反応促進剤と、
を含有する、ホルムアルデヒド不含の水性結合剤である。
上記水性結合剤は一般的に、水性エマルジョン、水溶液、あるいはイソプロパノール、エタノール、グリコール等の水溶性有機溶媒溶液、水と上記水溶性有機溶媒との混合溶媒の溶液等の形状で提供され、ポリマー(A)に含まれる酸と、アルカノールアミン(B)に含まれる水酸基とのエステル化反応によって硬化し、水溶性が水不溶性に変化し、熱可塑性が擬似熱可塑性に変化する。
上記擬似熱可塑性樹脂は、現在BASF社より商品名アクロデュア(Acrodur)として上市されており、水溶液タイプとしては950L,DS3530、水性エマルジョンタイプとしては958Dがある。
上記アクロデュアは、大凡120℃以上の温度で上記エステル化反応によって架橋が開始され、160℃以上の温度で硬化するが、架橋前の熱可塑性の状態でも充分な硬さを有し、取扱いが容易であり、しかも熱成形時には加熱により硬さが低下して一時的に熱可塑性になり(擬似熱可塑性)、良好な成形性を示し、高い成形精度が得られる。また上記アクロデュアの架橋はエステル化反応によるから、水のみが副成され、ホルムアルデヒド等の有害物質が副成されないという利点がある。
上記擬似熱可塑性樹脂は二種以上、例えば水溶液タイプと水性エマルジョンタイプとが混合されてもよいし、他の熱可塑性樹脂水性エマルジョン等が混合されてもよい。
上記擬似熱可塑性樹脂の詳細は、例えば特表2000−506940号公報に記載されている。
The pseudo thermoplastic resin used for the pseudo thermoplastic felt is
(A) 5 to 100% by weight of a polymer obtained by radical polymerization consisting of an ethylenically unsaturated acid anhydride or an ethylenically unsaturated dicarboxylic acid in which a carboxylic acid group can form an acid anhydride group;
(B) an alkanolamine having at least two hydroxyl groups;
A phosphorus-containing reaction accelerator less than 1.5% by mass with respect to the sum of (A) + (B);
An aqueous binder containing no formaldehyde.
The aqueous binder is generally provided in the form of an aqueous emulsion, an aqueous solution, a water-soluble organic solvent solution such as isopropanol, ethanol, or glycol, or a mixed solvent solution of water and the water-soluble organic solvent. It hardens | cures by esterification reaction of the acid contained in A) and the hydroxyl group contained in alkanolamine (B), water solubility changes to water insolubility, and thermoplasticity changes to pseudo thermoplasticity.
The pseudo thermoplastic resin is currently marketed by BASF under the trade name Acrodur, and there are 950L, DS3530 as an aqueous solution type, and 958D as an aqueous emulsion type.
The above acrodea is crosslinked by the esterification reaction at a temperature of approximately 120 ° C. or higher and is cured at a temperature of 160 ° C. or higher. However, the acrodure has sufficient hardness even in a thermoplastic state before crosslinking and is easy to handle. Moreover, during thermoforming, the hardness is reduced by heating and becomes temporarily thermoplastic (pseudo-thermoplastic), exhibits good moldability, and high molding accuracy is obtained. Moreover, since the cross-linking of the acrodure is based on an esterification reaction, there is an advantage that only water is by-produced and no harmful substances such as formaldehyde are by-produced.
Two or more of the above-mentioned pseudo thermoplastic resins, for example, an aqueous solution type and an aqueous emulsion type may be mixed, or other thermoplastic resin aqueous emulsions and the like may be mixed.
The details of the pseudo thermoplastic resin are described in, for example, JP 2000-506940 A.
上記熱可塑性フェルトに使用される熱可塑性樹脂としては、例えばアクリル酸エステル樹脂、メタクリル酸エステル樹脂、アイオノマー樹脂、エチレン−アクリル酸エチル(EEA)樹脂、アクリロニトリル・スチレン・アクリルゴム共重合(ASA)樹脂、アクリロニトリル・スチレン共重合(AS)樹脂、アクリロニトリル・塩素化ポリエチレン・スチレン共重合(ACS)樹脂、エチレン酢酸ビニル共重合(EVA)樹脂、エチレンビニルアルコール共重合(EVOH)樹脂、メタクリル樹脂(PMMA)、ポリブタジエン(BDR)、ポリスチレン(PS)、ポリエチレン(PE)、アクリロニトリル・ブタジエン・スチレン共重合(ABS)樹脂、塩素化ポリエチレン(CPE)、ポリ塩化ビニル(PVC)、ポリ塩化ビニリデン(PVDC)、ポリプロピレン(PP)、酢酸繊維素(セルロースアセテート:CA)樹脂、シンジオタクチックポリスチレン(SPS)、ポリオキシメチレン(=ポリアセタール)(POM)、ポリアミド(PA)、ポリイミド(PI)、ポリアミドイミド(PAI)、ポリエーテルイミド(PEI)、ポリアリレート(PAR)、熱可塑性ポリウレタン(TPU)エラストマー、熱可塑性エラストマー(TPE)、液晶ポリマー(LCP)、ポリエーテルエーテルケトン(PEEK)、ポリサルフォン(PSF)、ポリエーテルサルフォン(PES)、フッ素樹脂、ポリテトラフルオロエチレン(PTFE)、ポリエチレンテレフタレート(PET)、ポリカーボネート(PC)、ポリフェニレンエーテル(PPE)、変性PPE、ポリフェニレンサルファイド(PPS)、ポリブチレンテレフタレート(PBT)、ポリベンゾイミダゾール(PBI)、全芳香族ポリエステル(POB)等が例示される。
上記熱可塑性樹脂は、2種以上混合使用されてもよく、また熱可塑性樹脂の成形容易性を阻害しない程度で若干量の熱硬化性樹脂の1種または2種以上を混合使用してもよい。該熱可塑性樹脂は取り扱いが容易な点から水溶液、水性エマルジョン、水性ディスパージョンの形のものを使用することが好ましいが、有機溶剤溶液の形のものを使用してもよい。
Examples of the thermoplastic resin used in the thermoplastic felt include acrylic ester resin, methacrylic ester resin, ionomer resin, ethylene-ethyl acrylate (EEA) resin, acrylonitrile / styrene / acrylic rubber copolymer (ASA) resin. , Acrylonitrile / styrene copolymer (AS) resin, Acrylonitrile / chlorinated polyethylene / styrene copolymer (ACS) resin, Ethylene vinyl acetate copolymer (EVA) resin, Ethylene vinyl alcohol copolymer (EVOH) resin, Methacrylic resin (PMMA) , Polybutadiene (BDR), polystyrene (PS), polyethylene (PE), acrylonitrile-butadiene-styrene copolymer (ABS) resin, chlorinated polyethylene (CPE), polyvinyl chloride (PVC), polyvinylidene chloride PVDC), polypropylene (PP), cellulose acetate (CA) resin, syndiotactic polystyrene (SPS), polyoxymethylene (= polyacetal) (POM), polyamide (PA), polyimide (PI), polyamideimide (PAI), polyetherimide (PEI), polyarylate (PAR), thermoplastic polyurethane (TPU) elastomer, thermoplastic elastomer (TPE), liquid crystal polymer (LCP), polyetheretherketone (PEEK), polysulfone (PSF) , Polyethersulfone (PES), fluororesin, polytetrafluoroethylene (PTFE), polyethylene terephthalate (PET), polycarbonate (PC), polyphenylene ether (PPE), modified PPE, poly E double sulfide (PPS), polybutylene terephthalate (PBT), polybenzimidazole (PBI), wholly aromatic polyester (POB), and the like.
The above thermoplastic resins may be used in combination of two or more, and may be used by mixing one or more of a certain amount of thermosetting resin to the extent that does not impair the ease of molding of the thermoplastic resin. . The thermoplastic resin is preferably used in the form of an aqueous solution, an aqueous emulsion, or an aqueous dispersion from the viewpoint of easy handling, but may be used in the form of an organic solvent solution.
更に、上記成形性フェルト3に成形性を付与する手段としては、上記熱可塑性樹脂に代えて、あるいは上記熱可塑性樹脂と共に、融点が180℃以下である低融点熱可塑性樹脂繊維を使用する。該低融点熱可塑性樹脂繊維としては、例えば、ポリエチレン、ポリプロピレン、エチレン−酢酸ビニル共重合体、エチレン−エチルアクリレート共重合体等のポリオレフィン系繊維、ポリ塩化ビニル繊維、ポリウレタン繊維、ポリエステル繊維、ポリエステル共重合体繊維、ポリアミド繊維、ポリアミド共重合体繊維等がある。これらの低融点熱可塑性樹脂繊維は、単独あるいは2種以上組合わせて使用される。また、これらの低融点熱可塑性樹脂繊維を芯とし、融点が200℃以上の高融点繊維を鞘とした、あるいは融点が200℃以上の高融点繊維を芯とし、低融点熱可塑性樹脂繊維を鞘とした芯鞘構成の複合繊維等が使用される。
上記芯鞘構成の複合繊維を使用すると該フェルトの剛性が向上する。
該低融点熱可塑性樹脂繊維の繊度は、0.1dtex〜60dtexの範囲である。
上記低融点熱可塑性樹脂繊維は通常上記繊維に10〜50質量%混合される。
Further, as means for imparting moldability to the moldable felt 3, low-melting-point thermoplastic resin fibers having a melting point of 180 ° C. or lower are used instead of the thermoplastic resin or together with the thermoplastic resin. Examples of the low-melting point thermoplastic resin fiber include polyolefin fibers such as polyethylene, polypropylene, ethylene-vinyl acetate copolymer, ethylene-ethyl acrylate copolymer, polyvinyl chloride fiber, polyurethane fiber, polyester fiber, and polyester copolymer. There are polymer fibers, polyamide fibers, polyamide copolymer fibers and the like. These low melting point thermoplastic resin fibers are used alone or in combination of two or more. Further, these low melting point thermoplastic resin fibers are used as cores and high melting point fibers having a melting point of 200 ° C. or higher are used as sheaths, or high melting point fibers having melting points of 200 ° C. or higher are used as cores, and low melting point thermoplastic resin fibers are used as sheaths. A core-sheath composite fiber or the like is used.
When the composite fiber having the core-sheath configuration is used, the rigidity of the felt is improved.
The fineness of the low-melting point thermoplastic resin fiber is in the range of 0.1 dtex to 60 dtex.
The low-melting point thermoplastic resin fiber is usually mixed with the fiber in an amount of 10 to 50% by mass.
上記成形性フェルト3は、上記繊維のウェブのシートあるいはマットをニードルパンチングによって絡合する方法、あるいは繊維のウェブのシートあるいはマットが上記低融点熱可塑性樹脂繊維からなるか、あるいは上記低融点熱可塑性樹脂繊維が混合されている場合には該混合繊維のウェブをそのまま、あるいは該ウェブをニードルパンチングによって絡合した上で加熱して、該低融点熱可塑性樹脂繊維を軟化せしめて繊維相互を結着する方法、あるいは上記繊維シートまたはマットに合成樹脂を含浸あるいは混合して結着するか、あるいは上記繊維のウェブのシートまたはマットをニードルパンチングによって絡合した上で合成樹脂あるいは合成樹脂前駆体の粉末、溶液、エマルジョン、あるいはラテックスを混合、塗布あるいは含浸して結着する方法、上記繊維を編織する方法等によって製造される。
上記成形性フェルト3の目付量、厚みは原則任意に設定可能であるが、内装材6の軽量化の観点から、望ましくは、目付量50〜1000g/m2、更に望ましくは100〜500g/m2であり、形状保持の面から厚さは1.5mm以上とすることが望ましい。
上記成形性フェルト3に融点180℃以下の低融点熱可塑性樹脂繊維が10〜50質量%含まれていると、内装材6の成形性が向上する。
The formable felt 3 is formed by a method in which the fiber web sheet or mat is entangled by needle punching, or the fiber web sheet or mat is made of the low-melting thermoplastic resin fiber, or the low-melting thermoplasticity. When resin fibers are mixed, the mixed fiber web is heated as it is or after the web is entangled by needle punching to soften the low melting point thermoplastic resin fibers and bind the fibers to each other. Or the fiber sheet or mat is impregnated with or mixed with a synthetic resin, or the fiber web sheet or mat is entangled by needle punching and then the synthetic resin or synthetic resin precursor powder. , Mixed, coated or impregnated with solution, emulsion or latex How to sintering wear, it is produced by a method in which woven knitted the fibers.
The basis weight and thickness of the moldable felt 3 can be arbitrarily set in principle. From the viewpoint of reducing the weight of the interior material 6, the basis weight is preferably 50 to 1000 g / m 2 , more preferably 100 to 500 g / m. 2 and the thickness is preferably 1.5 mm or more from the surface of shape retention.
When the moldable felt 3 contains 10 to 50% by mass of a low melting point thermoplastic resin fiber having a melting point of 180 ° C. or less, the moldability of the interior material 6 is improved.
〔紙材料〕
紙材料1として用いられるのは多孔質パルプ繊維を90質量%以上含み、通気抵抗が0.07〜3.00kPa・s/mの範囲の紙である。
上記紙材料1の通気抵抗が0.07kPa・s/m未満の場合には吸音性能の良い内装材6が得られず、一方通気抵抗が3.00kPa・s/mを超える紙材料の場合には、成形性の良い内装材6が得られない。
[Paper materials]
The paper material 1 is a paper containing 90% by mass or more of porous pulp fibers and having a ventilation resistance in the range of 0.07 to 3.00 kPa · s / m.
When the paper material 1 has a ventilation resistance of less than 0.07 kPa · s / m, the interior material 6 with good sound absorption performance cannot be obtained. Cannot obtain the interior material 6 with good moldability.
(多孔質パルプ繊維)
上記多孔質パルプ繊維とは、繊維自体が、その表面で開口する細孔を多数有するものをいう。上記多孔質パルプ繊維は、非木材系植物繊維および/または木材系植物繊維からなり、通常針葉樹や広葉樹のチップを原料とし、叩解度がJIS P 8121−1995の4.カナディアン・スタンダード・フリーネスに規定されるカナダ標準型ろ水度で350〜650ml(CSF)の範囲で繊維の長径が5μm〜100μmの多孔質パルプ繊維である。
上記叩解は通常コニカルリファイナー、ディスクリファイナー等によって行われる。
上記多孔質パルプ繊維の平均長は0.2〜30mmの範囲であることが望ましく、長径は5〜100μmであることが望ましい。上記多孔質パルプ繊維の平均長が0.2mmに満たない場合は紙材料1中の繊維相互の絡み合いが不充分となって内装材6の強度が低下し、平均長が30mmを超えると繊維自体が糸まり状に絡み易くなり、繊維をシートにすることが困難となる。また繊維長径が5μmに満たない場合はシート密度が過大になり、またシート強度が低下し、繊維長径が100μmを超えると繊維自体の剛性が高くなって繊維相互の絡み合いが困難になる。
本発明の紙材料1に使用される多孔質パルプ繊維は二種以上混合使用されてもよく、また、上記多孔質パルプ繊維と通常繊維(非多孔質繊維)とを混合してもよい。なお、この場合の混合比率は内装材6の吸音性能を良好なものとするという観点から、多孔質パルプ繊維が90質量%以上含まれるべきであり、望ましくは95質量%以上、更に望ましくは100質量%含まれるべきである。
(Porous pulp fiber)
The said porous pulp fiber means that the fiber itself has many pores opened on the surface. The porous pulp fiber is made of non-wood plant fiber and / or wood plant fiber, and is usually made of softwood or hardwood chips, and the beating degree is JIS P 8121-1995 4. It is a porous pulp fiber having a long diameter of 5 μm to 100 μm within the range of 350 to 650 ml (CSF) with a Canadian standard freeness prescribed by Canadian Standard Freeness.
The above beating is usually performed by a conical refiner, a disc refiner, or the like.
The average length of the porous pulp fibers is desirably in the range of 0.2 to 30 mm, and the major axis is desirably 5 to 100 μm. When the average length of the porous pulp fibers is less than 0.2 mm, the entanglement between the fibers in the paper material 1 is insufficient, and the strength of the interior material 6 is reduced. When the average length exceeds 30 mm, the fibers themselves Becomes easily entangled in a string shape, making it difficult to form a fiber into a sheet. On the other hand, when the fiber major axis is less than 5 μm, the sheet density becomes excessive, and the sheet strength is lowered.
Two or more kinds of porous pulp fibers used in the paper material 1 of the present invention may be mixed and used, and the porous pulp fibers and normal fibers (non-porous fibers) may be mixed. The mixing ratio in this case should contain 90% by mass or more of porous pulp fiber, preferably 95% by mass or more, and more preferably 100% from the viewpoint of improving the sound absorption performance of the interior material 6. Should be included by mass%.
(通常繊維)
上記多孔質パルプ繊維と併用される通常繊維(非多孔質繊維)としては、例えばポリエステル繊維、ポリエチレン繊維、ポリプロピレン繊維、ポリアミド繊維、アクリル繊維、ウレタン繊維、ポリ塩化ビニル繊維、ポリ塩化ビニリデン繊維、アセテート繊維等の合成繊維、とうもろこしやサトウキビ等の植物から抽出された澱粉からなる生分解繊維(ポリ乳酸繊維)、パルプ、木綿、ヤシ繊維、麻繊維、竹繊維、ケナフ繊維等の天然繊維、ガラス繊維、炭素繊維、セラミック繊維、石綿繊維等の無機繊維、あるいはこれらの繊維を使用した繊維製品のスクラップを解繊して得られた再生繊維の1種または2種以上の繊維が使用されるが、例えばガラス繊維、炭素繊維、セラミック繊維、石綿繊維、ステンレス繊維等の無機繊維やポリメタフェニレンイソフタルアミド繊維、ポリ−p−フェニレンテレフタルアミド繊維等のアラミド繊維、ポリアリレート繊維、ポリエーテルエーテルケトン繊維、ポリフェニレンサルファイド繊維等の望ましくは融点が250℃以上の耐熱性合成繊維を混合使用すれば、耐熱性の極めて高い繊維シートが得られる。その中でも炭素繊維は焼却処理が可能で細片が飛散しにくい点で有用な無機繊維であり、アラミド繊維は比較的安価で入手し易い点で有用な難燃性合成繊維である。
(Normal fiber)
Examples of the normal fiber (non-porous fiber) used in combination with the porous pulp fiber include polyester fiber, polyethylene fiber, polypropylene fiber, polyamide fiber, acrylic fiber, urethane fiber, polyvinyl chloride fiber, polyvinylidene chloride fiber, and acetate. Synthetic fibers such as fibers, biodegradable fibers (polylactic acid fibers) made of starch extracted from plants such as corn and sugarcane, natural fibers such as pulp, cotton, palm fibers, hemp fibers, bamboo fibers, kenaf fibers, glass fibers In addition, inorganic fibers such as carbon fibers, ceramic fibers, asbestos fibers, or one or more kinds of recycled fibers obtained by defibrating scraps of textile products using these fibers are used. For example, inorganic fibers such as glass fiber, carbon fiber, ceramic fiber, asbestos fiber, stainless steel fiber, and polymetaphene If heat-resistant synthetic fibers having a melting point of 250 ° C. or higher, such as aramid fibers such as lenisophthalamide fibers and poly-p-phenylene terephthalamide fibers, polyarylate fibers, polyetheretherketone fibers and polyphenylene sulfide fibers, are preferably used. A fiber sheet with extremely high heat resistance can be obtained. Among them, carbon fiber is a useful inorganic fiber in that it can be incinerated and it is difficult for fine pieces to scatter, and aramid fiber is a flame-retardant synthetic fiber that is relatively inexpensive and easily available.
上記紙材料1の通気抵抗は0.07〜3.00kPa・s/mの範囲であるが、ここで、上記の通気抵抗(Pa・s/m)とは、通気性材料の通気の程度を表す尺度である。この通気抵抗の測定は定常流差圧測定方式により行われる。図1に示すように、シリンダー状の通気路W内に試験片Tを配置し、一定の通気量V(図中矢印の向き)の状態で図中矢印の始点側の通気路W内の圧力P1と、図中矢印の終点P2の圧力差を測定し、次式より通気抵抗Rを求めることが出来る。
R=ΔP/V
ここで、ΔP(=P1−P2):圧力差(Pa)、V:単位面積当りの通気量(m3/m2・s)である。
通気抵抗は、例えば、通気性試験機(製品名:KES−F8−AP1、カトーテック株式会社製、定常流差圧測定方式)によって測定することが出来る。
The ventilation resistance of the paper material 1 is in the range of 0.07 to 3.00 kPa · s / m. Here, the ventilation resistance (Pa · s / m) is the degree of ventilation of the breathable material. It is a measure to represent. This ventilation resistance is measured by a steady flow differential pressure measurement method. As shown in FIG. 1, a test piece T is arranged in a cylindrical air passage W, and the pressure in the air passage W on the start point side of the arrow in the figure in a state of a constant air flow V (the direction of the arrow in the figure). By measuring the pressure difference between P1 and the end point P2 of the arrow in the figure, the ventilation resistance R can be obtained from the following equation.
R = ΔP / V
Here, ΔP (= P1−P2): Pressure difference (Pa), V: Air flow rate per unit area (m 3 / m 2 · s).
The ventilation resistance can be measured by, for example, an air permeability tester (product name: KES-F8-AP1, manufactured by Kato Tech Co., Ltd., steady flow differential pressure measurement method).
上記紙材料1として、表面に多数の凹凸を形成した延伸性紙材料を使用してもよい。該延伸性紙材料を使用すると、吸音性能に優れかつ成形性の良い表皮材が得られる。 As the paper material 1, an extensible paper material having a large number of irregularities on the surface may be used. When the stretchable paper material is used, a skin material having excellent sound absorbing performance and good moldability can be obtained.
前記延伸性紙材料としては、表面に縮緬状の皺を形成したクレープ加工紙、表面に多数の突起を形成したエンボス加工紙、表面に縮緬状の皺と多数の突起を形成したクレープエンボス加工紙等が例示される。
上記クレープ加工紙は原料にクレープ加工を施したものであり、上記クレープ加工には、湿紙の状態でプレスロールやドクターブレードを用いて縦方向に圧縮して皺付けを行なうウェットクレープと、シートをヤンキードライヤーやカレンダーで乾燥した後ドクターブレード等を用いて縦方向に圧縮して皺付けを行なうドライクレープがある。
この場合次式で計算されるクレープ率が10〜50%であることが望ましい。
クレープ率(%)=(A/B)×100
A:紙抄造工程における抄紙速度
B:紙の巻き取り速度
即ちクレープ率とはペーパーウェブがクレーピングで縦方向(抄造方向)に圧縮される割合である。
該クレープ率が10%未満の場合には、クレープ加工紙の吸音性能が悪くなりかつ延伸性が不充分となって成形時に皺が発生し易くなり、一方該クレープ率が50%を越えると、やはり成形時に皺が発生し易くなる。
Examples of the stretchable paper material include crepe paper having a crimped wrinkle formed on the surface, embossed paper having a large number of protrusions formed on the surface, and crepe embossed paper having a crimped wrinkle and many protrusions formed on the surface. Etc. are exemplified.
The creped paper is obtained by creping a raw material. In the crepe processing, a wet crepe that is compressed in the vertical direction using a press roll or a doctor blade in a wet paper state and brazed, and a sheet There is a dry crepe that is dried with a Yankee dryer or calendar and then compressed in the longitudinal direction using a doctor blade or the like.
In this case, it is desirable that the crepe rate calculated by the following formula is 10 to 50%.
Crepe rate (%) = (A / B) × 100
A: Paper making speed in the paper making process B: Paper winding speed That is, the crepe rate is the ratio at which the paper web is compressed in the longitudinal direction (paper making direction) by creping.
When the crepe rate is less than 10%, the sound absorbing performance of the creped paper is deteriorated and the stretchability is insufficient, and wrinkles are easily generated during molding. On the other hand, when the crepe rate exceeds 50%, Again, wrinkles are likely to occur during molding.
上記エンボス加工紙は表面に多数の凹凸を設けたロール(エンボスロール)やプレート(エンボスプレート)を原紙に押圧し、紙の表面に多数の突起を形成したものであり、該突起の高さは0.02〜2.00mmであり、かつ突起数は20〜200個/cm2であることが望ましい。該突起高さが0.02mm未満の場合には、該エンボス加工紙の吸音性能が悪くなり、かつ延伸性が不充分となって成形時に皺が発生し易くなり、一方該突起高さが2.00mmを超えても成形時に皺が発生し易くなる。また突起数が20個/cm2未満の場合には、該エンボス加工紙の吸音性能が悪くなり、また延伸性が不充分となって成形時に皺が発生し易くなり、一方突起数が200個/cm2を超えても、該エンボス加工紙の吸音性能が悪くなる。
なお図2に示されるエンボス加工紙1a(延伸性紙材料)には表面に多数の突起1bが形成されており、該突起1bの高さは、図2に示す「h」に相当する。上記原紙としてクレープ加工紙を使用すればエンボスクレープ加工紙となる。
ところで、紙材料の目付量は、通常10〜60g/m2程度であるが、本発明に係る紙材料の目付量は、望ましくは15〜50g/m2である。目付量が小さすぎると通気抵抗が低くなりすぎて望ましい吸音性能が得られず、逆に大きすぎると通気抵抗が高くなりすぎて吸音性能が低下する。
The embossed paper is formed by pressing a roll (embossing roll) or plate (embossing plate) having a large number of irregularities on the surface against the base paper to form a large number of protrusions on the surface of the paper. It is desirable that the thickness is 0.02 to 2.00 mm and the number of protrusions is 20 to 200 / cm 2 . When the height of the protrusion is less than 0.02 mm, the sound absorption performance of the embossed paper is deteriorated and the stretchability is insufficient so that wrinkles are easily generated during molding. Even if it exceeds 0.000 mm, wrinkles are likely to occur during molding. On the other hand, when the number of protrusions is less than 20 / cm 2 , the sound absorption performance of the embossed paper is deteriorated, the stretchability is insufficient, and wrinkles are easily generated during molding, while the number of protrusions is 200 Even if it exceeds / cm 2 , the sound absorbing performance of the embossed paper deteriorates.
The embossed paper 1a (extensible paper material) shown in FIG. 2 has a large number of protrusions 1b on the surface, and the height of the protrusions 1b corresponds to “h” shown in FIG. If crepe paper is used as the base paper, it becomes embossed crepe paper.
By the way, the basis weight of the paper material is usually about 10 to 60 g / m 2 , but the basis weight of the paper material according to the present invention is desirably 15 to 50 g / m 2 . If the basis weight is too small, the ventilation resistance becomes too low to obtain the desired sound absorption performance, while if too large, the ventilation resistance becomes too high and the sound absorption performance is lowered.
〔通気性表装材〕
通気性表装材2としては、通常上記成形性フェルト3で使用された繊維と同様な繊維からなるシートまたはマットが用いられる。
該通気性表装材2で用いられる繊維も該成形性フェルト3と同様に、融点が180℃以下である低融点熱可塑性樹脂繊維を使用してもよい。またその際用いられる低融点熱可塑性樹脂繊維の繊度は、0.1dtex〜60dtexの範囲であり、上記低融点熱可塑性樹脂繊維は通常上記繊維に1〜50質量%混合される。
(Breathable exterior material)
As the breathable outer covering material 2, a sheet or mat made of fibers similar to those used in the moldable felt 3 is usually used.
As with the moldable felt 3, low melting point thermoplastic resin fibers having a melting point of 180 ° C. or lower may be used as the fibers used in the breathable outer covering material 2. Further, the fineness of the low melting point thermoplastic resin fiber used in this case is in the range of 0.1 dtex to 60 dtex, and the low melting point thermoplastic resin fiber is usually mixed with the fiber in an amount of 1 to 50% by mass.
上記通気性表装材2として使用される繊維シートまたはマットは、成形性フェルト3の製造方法において記載したものと同様に、上記繊維のウェブのシートあるいはマットをニードルパンチングによって絡合する方法、あるいは繊維のウェブのシートあるいはマットが上記低融点熱可塑性樹脂繊維からなるか、あるいは上記低融点熱可塑性樹脂繊維が混合されている場合には該混合繊維のウェブをそのまま、あるいは該ウェブをニードルパンチングによって絡合した上で加熱して、該低融点熱可塑性樹脂繊維を軟化せしめて繊維相互を結着する方法、あるいは上記繊維シートまたはマットに合成樹脂を含浸あるいは混合して結着するか、あるいは上記繊維のウェブのシートまたはマットをニードルパンチングによって絡合した上で合成樹脂あるいは合成樹脂前駆体の粉末、溶液、エマルジョン、あるいはラテックスを混合、塗布あるいは含浸して結着する方法、上記繊維を編織する方法等によって製造される。
上記繊維シートまたはマットの目付量は内装材6の好ましい意匠性や外観という観点から、通常50〜500g/m2、厚みは通常1〜10mmに設定される。
The fiber sheet or mat used as the breathable outer covering material 2 is a method in which the fiber web sheet or mat is entangled by needle punching in the same manner as described in the method for producing the moldable felt 3 or fiber. If the web sheet or mat is made of the low-melting point thermoplastic resin fiber, or if the low-melting point thermoplastic resin fiber is mixed, the web of the mixed fiber is left as it is or the web is entangled by needle punching. A method of softening the low-melting point thermoplastic resin fibers and bonding the fibers together by heating after combining, or impregnating or mixing the synthetic resin in the fiber sheet or mat, or binding the fibers The web sheet or mat is entangled by needle punching and then the synthetic resin Powder had synthetic resin precursor, solutions, emulsions or mixed latex, a method of forming wear by coating or impregnation, is prepared by a method in which woven knitted the fibers.
The basis weight of the fiber sheet or mat is usually set to 50 to 500 g / m 2 and the thickness is usually set to 1 to 10 mm from the viewpoint of preferable design and appearance of the interior material 6.
上記通気性表装材2を床敷材として使用する場合には、通常カーペットのような起毛布を使用する。上記カーペットには通常カットパイルやループパイルのようなパイル層が形成されるが、上記パイル層を形成するにはタフティング、ニードルパンチング、あるいは静電植毛等が適用される。
従来のカーペットにあっては、通常吸音材料としてポリエステル繊維やポリプロピレン繊維等の有機合成繊維からなるフェルトが裏打ちされている。
本発明の内装材6においては、上記フェルトに代えて上記紙材料1を裏打ちすることで、従来のフェルトを裏打ちしたカーペットと比べて吸音性能に優れ、該フェルトの軽量化や厚さの低減が可能になり、その分厚みが薄くなり、その上重量が大幅に軽減される。
上記フェルトに使用される有機合成繊維は製造工程において二酸化炭素を排出する。しかし本発明の紙材料は原料として製造工程で二酸化炭素を殆んど排出されない天然パルプ繊維を使用しているから、二酸化炭素の排出量を削減できると共に、天然パルプ繊維は腐朽性があるために廃棄物処理も容易であり、またバイオマスエネルギー(例えばバイオエタノールの原料)としても使用できる。
When the breathable outer covering material 2 is used as a floor covering material, a raised cloth such as a carpet is usually used. A pile layer such as a cut pile or a loop pile is usually formed on the carpet. Tufting, needle punching, electrostatic flocking, or the like is applied to form the pile layer.
In conventional carpets, a felt made of organic synthetic fibers such as polyester fibers and polypropylene fibers is usually lined as a sound absorbing material.
In the interior material 6 of the present invention, the paper material 1 is lined instead of the felt, so that the sound absorbing performance is superior to the carpet lined with the conventional felt, and the weight of the felt is reduced and the thickness is reduced. It becomes possible, the thickness is reduced correspondingly, and the weight is greatly reduced.
The organic synthetic fiber used for the felt emits carbon dioxide in the production process. However, since the paper material of the present invention uses natural pulp fiber that hardly emits carbon dioxide in the production process as a raw material, carbon dioxide emissions can be reduced and natural pulp fiber is decaying. Waste disposal is also easy, and it can be used as biomass energy (for example, a raw material for bioethanol).
〔合成樹脂〕
上記した通気性表装材2および/または紙材料1にあっては、剛性や成形性を付与するために、合成樹脂等を塗布または含浸または混合させてもよい。合成樹脂としては、例えば熱可塑性樹脂及び/又は熱硬化性樹脂が例示される。
[Synthetic resin]
In the above-described breathable outer covering material 2 and / or paper material 1, synthetic resin or the like may be applied, impregnated, or mixed in order to impart rigidity or moldability. Examples of the synthetic resin include a thermoplastic resin and / or a thermosetting resin.
上記熱可塑性樹脂としては上記熱可塑性フェルトとして成形性フェルト3に用いたものと同様に、例えばアクリル酸エステル樹脂、メタクリル酸エステル樹脂、アイオノマー樹脂、エチレン−アクリル酸エチル(EEA)樹脂、アクリロニトリル・スチレン・アクリルゴム共重合(ASA)樹脂、アクリロニトリル・スチレン共重合(AS)樹脂、アクリロニトリル・塩素化ポリエチレン・スチレン共重合(ACS)樹脂、エチレン酢酸ビニル共重合(EVA)樹脂、エチレンビニルアルコール共重合(EVOH)樹脂、メタクリル樹脂(PMMA)、ポリブタジエン(BDR)、ポリスチレン(PS)、ポリエチレン(PE)、アクリロニトリル・ブタジエン・スチレン共重合(ABS)樹脂、塩素化ポリエチレン(CPE)、ポリ塩化ビニル(PVC)、ポリ塩化ビニリデン(PVDC)、ポリプロピレン(PP)、酢酸繊維素(セルロースアセテート:CA)樹脂、シンジオタクチックポリスチレン(SPS)、ポリオキシメチレン(=ポリアセタール)(POM)、ポリアミド(PA)、ポリイミド(PI)、ポリアミドイミド(PAI)、ポリエーテルイミド(PEI)、ポリアリレート(PAR)、熱可塑性ポリウレタン(TPU)エラストマー、熱可塑性エラストマー(TPE)、液晶ポリマー(LCP)、ポリエーテルエーテルケトン(PEEK)、ポリサルフォン(PSF)、ポリエーテルサルフォン(PES)、フッ素樹脂、ポリテトラフルオロエチレン(PTFE)、ポリエチレンテレフタレート(PET)、ポリカーボネート(PC)、ポリフェニレンエーテル(PPE)、変性PPE、ポリフェニレンサルファイド(PPS)、ポリブチレンテレフタレート(PBT)、ポリベンゾイミダゾール(PBI)、全芳香族ポリエステル(POB)等が例示される。このような熱可塑性樹脂は、上記通気性表装材2あるいは紙材料1に含浸および/または塗布および/または混合されて、成形形状保持性および剛性を向上せしめる。 Examples of the thermoplastic resin are the same as those used for the moldable felt 3 as the thermoplastic felt, such as acrylic ester resin, methacrylic ester resin, ionomer resin, ethylene-ethyl acrylate (EEA) resin, acrylonitrile / styrene.・ Acrylic rubber copolymer (ASA) resin, acrylonitrile / styrene copolymer (AS) resin, acrylonitrile / chlorinated polyethylene / styrene copolymer (ACS) resin, ethylene vinyl acetate copolymer (EVA) resin, ethylene vinyl alcohol copolymer ( EVOH resin, methacrylic resin (PMMA), polybutadiene (BDR), polystyrene (PS), polyethylene (PE), acrylonitrile-butadiene-styrene copolymer (ABS) resin, chlorinated polyethylene (CPE), polyvinyl chloride (PVC), polyvinylidene chloride (PVDC), polypropylene (PP), cellulose acetate (CA) resin, syndiotactic polystyrene (SPS), polyoxymethylene (= polyacetal) (POM), polyamide (PA) ), Polyimide (PI), polyamideimide (PAI), polyetherimide (PEI), polyarylate (PAR), thermoplastic polyurethane (TPU) elastomer, thermoplastic elastomer (TPE), liquid crystal polymer (LCP), polyetherether Ketone (PEEK), polysulfone (PSF), polyethersulfone (PES), fluororesin, polytetrafluoroethylene (PTFE), polyethylene terephthalate (PET), polycarbonate (PC), polyphenylene ether Ether (PPE), modified PPE, polyphenylene sulfide (PPS), polybutylene terephthalate (PBT), polybenzimidazole (PBI), wholly aromatic polyester (POB), and the like. Such a thermoplastic resin is impregnated and / or applied and / or mixed with the air permeable covering material 2 or the paper material 1 to improve the shape retention and rigidity.
上記熱可塑性樹脂は、2種以上混合使用されてもよく、また熱可塑性樹脂の成形容易性を阻害しない程度で若干量の熱硬化性樹脂の1種または2種以上を混合使用してもよい。該熱可塑性樹脂は取り扱いが容易な点から水溶液、水性エマルジョン、水性ディスパージョンの形のものを使用することが好ましいが、有機溶剤溶液の形のものを使用してもよい。 The above thermoplastic resins may be used in combination of two or more, and may be used by mixing one or more of a certain amount of thermosetting resin to the extent that does not impair the ease of molding of the thermoplastic resin. . The thermoplastic resin is preferably used in the form of an aqueous solution, an aqueous emulsion, or an aqueous dispersion from the viewpoint of easy handling, but may be used in the form of an organic solvent solution.
上記熱硬化性樹脂としては上記熱硬化性フェルトとして成形性フェルト3に用いたのと同様に、例えばウレタン系樹脂、メラミン系樹脂、熱硬化型アクリル系樹脂、特に加熱によりエステル結合を形成して硬化する熱硬化性アクリル系樹脂、尿素系樹脂、フェノール系樹脂、エポキシ系樹脂、熱硬化型ポリエステル系樹脂等が使用されるが、該合成樹脂を生成するウレタン系樹脂プレポリマー、尿素系樹脂プレポリマー(初期縮合体)、フェノール系樹脂プレポリマー(初期縮合体)、ジアリルフタレートプレポリマー、アクリルオリゴマー、多価イソシアナート、メタクリルエステルモノマー、ジアリルフタレートモノマー等のプレポリマー、オリゴマー、モノマー等の合成樹脂前駆体が使用されてもよい。該熱硬化性樹脂も取り扱いが容易な点から、水溶液、水性エマルジョン、水性ディスパーションの形のものを使用することが好ましいが、有機溶剤溶液の形のものを使用してもよい。
上記熱硬化性樹脂あるいは合成樹脂前駆体は二種以上混合使用されてもよい。
上記合成樹脂、特に熱硬化性樹脂の添加は、上記通気性表装材2あるいは紙材料1の成形形状保持性と剛性を共に向上せしめる。
As the thermosetting resin, for example, a urethane resin, a melamine resin, a thermosetting acrylic resin, particularly an ester bond formed by heating, as used in the moldable felt 3 as the thermosetting felt. Thermosetting acrylic resins, urea resins, phenolic resins, epoxy resins, thermosetting polyester resins, and the like that are cured are used. Urethane resin prepolymers and urea resin prepolymers that produce the synthetic resins are used. Polymers (initial condensates), phenolic resin prepolymers (initial condensates), diallyl phthalate prepolymers, acrylic oligomers, polyvalent isocyanates, methacrylic ester monomers, prepolymers such as diallyl phthalate monomers, synthetic resins such as oligomers and monomers Precursors may be used. The thermosetting resin is preferably used in the form of an aqueous solution, an aqueous emulsion, or an aqueous dispersion because it is easy to handle, but may be used in the form of an organic solvent solution.
Two or more of the above thermosetting resins or synthetic resin precursors may be used in combination.
The addition of the synthetic resin, particularly the thermosetting resin, improves both the shape retention and rigidity of the breathable outer covering material 2 or the paper material 1.
また、特に本発明で使用される熱硬化性樹脂として望ましいのは、フェノール系樹脂である。該フェノール系樹脂には、フェノール系化合物に対してホルムアルデヒド類を過剰にしてアルカリ触媒で反応することによって得られるレゾールと、ホルムアルデヒド類に対してフェノールを過剰にして酸触媒で反応することによって得られるノボラックの二つの型がある。該レゾールはフェノールとホルムアルデヒドが付加した種々のフェノールアルコールの混合物からなり、通常は水溶液で提供される。該ノボラックはフェノールアルコールに更にフェノールが縮合したジヒドロキシジフェニルメタン系の種々な誘導体からなり、通常は粉末で提供される。
本発明において望ましいフェノール系樹脂は、フェノール−アルキルレゾルシン共縮合物である。該フェノール−アルキルレゾルシン共縮合物は、該共縮合物(初期縮合物)の水溶液の安定性が良く、かつフェノールのみからなる縮合物(初期縮合物)に比較して、常温で長期間保存することが出来るという利点がある。また該水溶液を上記通気性表装材2や紙材料1に含浸、塗布、あるいは混合させ、プレキュアして得られる該通気性表装材2や紙材料1の安定性が良く、該通気性表装材2や紙材料1を長期間保存しても成形性を喪失しない。また更にアルキルレゾルシンはホルムアルデヒド類との反応性が高く、遊離アルデヒドを捕捉して反応するので、樹脂中の遊離アルデヒド量が少なくなる等の利点も有する。
エストニア産オイルシェールの乾留によって得られる多価フェノール混合物は安価であり、かつ5−メチルレゾルシンのほか反応性の高い各種アルキルレゾルシンを多量に含むので、本発明において特に好ましい多価フェノール原料である。
上記フェノール系樹脂には、その製造の際に必要に応じて触媒またはpH調整剤を混合してもよい。更に、本発明のフェノール系樹脂の初期縮合物(初期共縮合物を含む)には、ホルムアルデヒド類あるいはアルキロール化トリアゾン誘導体等の硬化剤を添加混合してもよい。更にまた、水溶性のフェノール系樹脂を用いる場合、その安定性を改良するために、フェノール系樹脂をスルホメチル化および/またはスルフィメチル化してもよい。
Further, a phenolic resin is particularly desirable as the thermosetting resin used in the present invention. The phenolic resin can be obtained by reacting with phenolic compounds in an excess of formaldehyde and reacting with an alkali catalyst, and by reacting with phenolic compounds in excess of phenol with an acid catalyst. There are two types of novolak. The resole consists of a mixture of various phenol alcohols with added phenol and formaldehyde, and is usually provided in an aqueous solution. The novolak is composed of various derivatives of dihydroxydiphenylmethane based on phenol condensed with phenol alcohol, and is usually provided in powder form.
A desirable phenolic resin in the present invention is a phenol-alkylresorcin cocondensate. The phenol-alkylresorcin co-condensate has good stability of the aqueous solution of the co-condensate (initial condensate) and is stored for a long time at room temperature as compared with a condensate (initial condensate) composed only of phenol. There is an advantage that you can. Further, the breathable surface covering material 2 and the paper material 1 obtained by impregnating, coating, or mixing the air permeable surface covering material 2 and the paper material 1 and pre-curing have good stability. Even if the paper material 1 is stored for a long time, the moldability is not lost. Furthermore, alkylresorcin has a high reactivity with formaldehydes and captures and reacts with a free aldehyde, so that it also has an advantage of reducing the amount of free aldehyde in the resin.
A polyhydric phenol mixture obtained by dry distillation of an Estonia oil shale is inexpensive and contains a large amount of highly reactive various alkylresorcins in addition to 5-methylresorcin. Therefore, it is a particularly preferable polyhydric phenol raw material in the present invention.
In the production of the phenolic resin, a catalyst or a pH adjuster may be mixed as necessary. Furthermore, a hardener such as formaldehyde or an alkylolated triazone derivative may be added to and mixed with the initial condensate (including the initial cocondensate) of the phenolic resin of the present invention. Furthermore, when a water-soluble phenolic resin is used, the phenolic resin may be sulfomethylated and / or sulfimethylated to improve its stability.
本発明で使用する合成樹脂あるいは合成樹脂前駆体には、更に、炭酸カルシウム、炭酸マグネシウム、硫酸バリウム、硫酸カルシウム、亜硫酸カルシウム、燐酸カルシウム、水酸化カルシウム、水酸化マグネシウム、水酸化アルミニウム、酸化マグネシウム、酸化チタン、酸化鉄、酸化亜鉛、アルミナ、シリカ、コロイダルシリカ、雲母、珪藻土、ドロマイト、石膏、タルク、クレー、アスベスト、マイカ、ケイ酸カルシウム、ベントナイト、ホワイトカーボン、カーボンブラック、鉄粉、アルミニウム粉、ガラス粉、石粉、高炉スラグ、フライアッシュ、セメント、ジルコニア粉等の無機充填材;天然ゴムまたはその誘導体;スチレン−ブタジエンゴム、アクリロニトリル−ブタジエンゴム、クロロプレンゴム、エチレン−プロピレンゴム、イソプレンゴム、イソプレン−イソブチレンゴム等の合成ゴム;ポリビニルアルコール、アルギン酸ナトリウム、澱粉、澱粉誘導体、ニカワ、ゼラチン、血粉、メチルセルロース、カルボキシメチルセルロース、ヒドロキシエチルセルロース、ポリアクリル酸塩、ポリアクリルアミド等の水溶性高分子や天然ガム類;木粉、クルミ粉、ヤシガラ粉、小麦粉、米粉等の有機充填材;ステアリン酸、パルミチン酸等の高級脂肪酸、パルミチルアルコール、ステアリルアルコール等の高級アルコール;ブチリルステアレート、グリセリンモノステアレート等の脂肪酸のエステル類;脂肪酸アミド類;カルナバワックス等の天然ワックス類、合成ワックス類;パラフィン類、パラフィン油、シリコンオイル、シリコン樹脂、フッ素樹脂、ポリビニルアルコール、グリス等の離型剤;アゾジカーボンアミド、ジニトロソペンタメチレンテトラミン、P,P’−オキシビス(ベンゼンスルホニルヒドラジド)、アゾビス−2,2’−(2−メチルグロピオニトリル)等の有機発泡剤;重炭酸ナトリウム、重炭酸カリウム、重炭酸アンモニウム等の無機発泡剤;シラスバルーン、パーライト、ガラスバルーン、発泡ガラス、中空セラミックス等の中空粒体;発泡ポリエチレン、発泡ポリスチレン、発泡ポリプロピレン等のプラスチック発泡体や発泡粒;顔料、染料、酸化防止剤、帯電防止剤、結晶化促進剤、燐系化合物、窒素系化合物、硫黄系化合物、ホウ素系化合物、臭素系化合物、グアニジン系化合物、燐酸塩系化合物、燐酸エステル系化合物、アミノ系樹脂等の難燃剤、防炎剤、撥水剤、撥油剤、防虫剤、防腐剤、ワックス類、界面活性剤、滑剤、老化防止剤、紫外線吸収剤;DBP、DOP、ジシクロヘキシルフタレートのようなフタル酸エステル系可塑剤やその他のトリクレジルホスフェート等の可塑剤等を添加、混合してもよい。 The synthetic resin or synthetic resin precursor used in the present invention further includes calcium carbonate, magnesium carbonate, barium sulfate, calcium sulfate, calcium sulfite, calcium phosphate, calcium hydroxide, magnesium hydroxide, aluminum hydroxide, magnesium oxide, Titanium oxide, iron oxide, zinc oxide, alumina, silica, colloidal silica, mica, diatomaceous earth, dolomite, gypsum, talc, clay, asbestos, mica, calcium silicate, bentonite, white carbon, carbon black, iron powder, aluminum powder, Inorganic fillers such as glass powder, stone powder, blast furnace slag, fly ash, cement, zirconia powder; natural rubber or derivatives thereof; styrene-butadiene rubber, acrylonitrile-butadiene rubber, chloroprene rubber, ethylene-propylene rubber Synthetic rubbers such as isoprene rubber and isoprene-isobutylene rubber; water-soluble polymers such as polyvinyl alcohol, sodium alginate, starch, starch derivatives, glue, gelatin, blood powder, methylcellulose, carboxymethylcellulose, hydroxyethylcellulose, polyacrylate, and polyacrylamide Organic gums such as wood powder, walnut powder, coconut powder, wheat flour and rice flour; higher fatty acids such as stearic acid and palmitic acid; higher alcohols such as palmityl alcohol and stearyl alcohol; butyryl stearate and glycerin Esters of fatty acids such as monostearate; fatty acid amides; natural waxes such as carnauba wax, synthetic waxes; paraffins, paraffin oil, silicone oil, silicone resin, fluororesin, polyvinyl Mold release agents such as alcohol and grease; organic compounds such as azodicarbonamide, dinitrosopentamethylenetetramine, P, P′-oxybis (benzenesulfonylhydrazide), azobis-2,2 ′-(2-methylgropionitrile) Foaming agent; inorganic foaming agent such as sodium bicarbonate, potassium bicarbonate, ammonium bicarbonate; hollow particles such as shirasu balloon, perlite, glass balloon, foamed glass, hollow ceramics; plastic such as foamed polyethylene, foamed polystyrene, foamed polypropylene, etc. Foam and foam particles: pigments, dyes, antioxidants, antistatic agents, crystallization accelerators, phosphorus compounds, nitrogen compounds, sulfur compounds, boron compounds, bromine compounds, guanidine compounds, phosphate compounds Compounds, phosphate compounds, flame retardants such as amino resins, flame retardants, water repellents, repellents Oils, insect repellents, preservatives, waxes, surfactants, lubricants, anti-aging agents, UV absorbers; phthalate plasticizers such as DBP, DOP, dicyclohexyl phthalate and other plastics such as tricresyl phosphate An agent or the like may be added and mixed.
また、撥水撥油剤としては、天然ワックス、合成ワックス、フッ素樹脂、シリコン系樹脂等がある。 Examples of the water / oil repellent include natural wax, synthetic wax, fluororesin, and silicon resin.
上記通気性表装材2あるいは紙材料1に上記合成樹脂等を塗布含浸するには、通常上記合成樹脂の水性エマルジョンあるいは水性ディスパーションに該通気性表装材2あるいは紙材料1を浸漬するか、あるいはナイフコーター、ロールコーター、フローコーター等によって塗布する。
上記樹脂を含浸または塗布した上記通気性表装材2あるいは紙材料1中の樹脂量を調節するには、樹脂を含浸または塗布後、該通気性表装材2あるいは紙材料1を絞りロールやプレス盤を使用して絞る。この場合、該通気性表装材2あるいは紙材料1はその厚みを減少させるが、該通気性表装材2あるいは紙材料1として繊維シートまたはマットを用いた場合には、該繊維シートまたはマットが低融点熱可塑性樹脂繊維からなるか、あるいは低融点熱可塑性樹脂繊維が含まれている場合には、上記樹脂含浸前に該繊維シートまたはマットを加熱して低融点熱可塑性樹脂繊維を溶融させ、繊維を該溶融物によって結着しておくことが望ましい。そうすると該通気性表装材2あるいは紙材料1としての繊維シートまたはマットは強度および剛性が更に向上し、樹脂含浸の際の作業性が向上し、また絞り後の厚みの復元も顕著になる。
上記通気性表装材2あるいは紙材料1としての繊維シートまたはマットに上記樹脂を含浸または塗布した後は、上記通気性表装材2あるいは紙材料1を常温または加熱して乾燥させる。
上記樹脂の含浸量は通常10g/m2〜100g/m2程度とする。この程度の樹脂含浸量であれば、上記通気性表装材2あるいは紙材料1の通気抵抗に殆んど影響を及ぼさない。
In order to apply and impregnate the above breathable surface covering material 2 or paper material 1 with the above synthetic resin or the like, the breathable surface covering material 2 or paper material 1 is usually immersed in an aqueous emulsion or aqueous dispersion of the above synthetic resin, or Apply with a knife coater, roll coater, flow coater, etc.
In order to adjust the amount of resin in the air-permeable covering material 2 or paper material 1 impregnated or coated with the resin, after impregnating or applying the resin, the air-permeable covering material 2 or paper material 1 is drawn into a squeeze roll or press machine. Squeeze using. In this case, the thickness of the air permeable covering material 2 or the paper material 1 is reduced. However, when a fiber sheet or mat is used as the air permeable covering material 2 or the paper material 1, the fiber sheet or mat is low. When the thermoplastic resin fiber is composed of a melting point thermoplastic resin fiber or contains a low melting point thermoplastic resin fiber, the fiber sheet or mat is heated before the resin impregnation to melt the low melting point thermoplastic resin fiber. It is desirable to bind with the melt. As a result, the fiber sheet or mat as the breathable outer covering material 2 or the paper material 1 is further improved in strength and rigidity, the workability at the time of resin impregnation is improved, and the restoration of the thickness after drawing is also remarkable.
After the resin is impregnated or coated on the fiber sheet or mat as the air-permeable covering material 2 or the paper material 1, the air-permeable covering material 2 or the paper material 1 is dried at room temperature or by heating.
Impregnated amount of the resin is usually 10g / m 2 ~100g / m 2 approximately. With this amount of resin impregnation, there is almost no influence on the ventilation resistance of the air-permeable outer covering material 2 or the paper material 1.
(難燃剤)
また、上記通気性表装材2、紙材料1、あるいは成形性フェルト3には、難燃剤が添加されてもよい。上記難燃剤としては、例えば燐系難燃剤、窒素系難燃剤、硫黄系難燃剤、ホウ素系難燃剤、臭素系難燃剤、グアニジン系難燃剤、燐酸塩系難燃剤、燐酸エステル系難燃剤、アミノ樹脂系難燃剤、膨張黒鉛等がある。
本発明の自動車用内装材6であれば、特に水に難溶または不溶の粉末状の固体難燃剤が使用されることが望ましい。水に難溶または不溶の粉末状の固体難燃剤は本発明の内装材6に耐水性、耐久性に優れた難燃性を付与する。特に本発明の通気性表装材2、紙材料1、あるいは成形性フェルト3は粗構造を有しているから、上記粉末状の固体難燃剤が内部にまで円滑に浸透して高度な難燃性ないし不燃性を付与する。
(Flame retardants)
In addition, a flame retardant may be added to the breathable outer covering material 2, the paper material 1, or the moldable felt 3. Examples of the flame retardant include phosphorus flame retardant, nitrogen flame retardant, sulfur flame retardant, boron flame retardant, bromine flame retardant, guanidine flame retardant, phosphate flame retardant, phosphate ester flame retardant, amino acid Resin-based flame retardant, expanded graphite, etc.
In the case of the automobile interior material 6 of the present invention, it is particularly desirable to use a powdery solid flame retardant that is hardly soluble or insoluble in water. The powdery solid flame retardant that is hardly soluble or insoluble in water imparts flame resistance excellent in water resistance and durability to the interior material 6 of the present invention. In particular, since the air-permeable outer covering material 2, the paper material 1, or the moldable felt 3 of the present invention has a rough structure, the above-mentioned powdered solid flame retardant smoothly penetrates into the interior and has high flame resistance. Or impart nonflammability.
〔自動車用内装材〕
上記通気性表装材2、紙材料1、成形性フェルト3、非通気性樹脂シート4、多孔質マット5をこの順に積層することで、例えば図3に示すような自動車床敷用内装材6となる。
本実施形態において、上記通気性表装材2と上記紙材料1、上記紙材料1と上記成形性フェルト3との接着には必要とあれば通気性接着剤が適用される。上記通気性接着剤において使用される接着剤は、通常の溶液型や水性エマルジョン型の接着剤や、粉末状、くもの巣状、溶液型、あるいは水性エマルジョン型のホットメルト接着剤等が使用される。粉末状、くもの巣状のホットメルト接着剤の場合には多孔性接着剤層となるため通気性を確保でき、上記通気性表装材2、紙材料1、成形性フェルト3の通気性を阻害しない。
溶液型あるいは水性エマルジョン型の接着剤の場合にはスプレー塗装あるいはシルク印刷塗装、オフセット印刷塗装等によって点状に接着剤を塗布し、上記通気性表装材2、紙材料1、成形性フェルト3の通気性を確保する。
上記成形性フェルト3と上記非通気性樹脂シート4、上記非通気性樹脂シート4と上記多孔質マット5との接着の場合は通気性を考慮する必要がないので、上記通気性接着剤に限らず周知の接着方法が適用できる。
なお、本発明において、通気性表装材2、紙材料1、成形性フェルト3は、それぞれを接着以外の方法、例えば溶着、融着等の方法で接合してもよい。
[Automobile interior materials]
By laminating the breathable outer covering material 2, the paper material 1, the moldable felt 3, the non-breathable resin sheet 4 and the porous mat 5 in this order, for example, an interior material 6 for an automobile flooring as shown in FIG. Become.
In this embodiment, a breathable adhesive is applied to the breathable facing material 2 and the paper material 1 and the paper material 1 and the moldable felt 3 if necessary. As the adhesive used in the air-permeable adhesive, a normal solution type or aqueous emulsion type adhesive, a powder type, a web type, a solution type, or an aqueous emulsion type hot melt adhesive, etc. are used. The In the case of a hot melt adhesive in the form of a powder or a web, a porous adhesive layer is used so that air permeability can be secured, and the air permeability of the air permeable covering material 2, paper material 1, and moldable felt 3 is inhibited. do not do.
In the case of a solution-type or water-emulsion-type adhesive, the adhesive is applied in the form of dots by spray coating, silk printing coating, offset printing coating, or the like. Ensure breathability.
In the case of adhesion between the moldable felt 3 and the non-breathable resin sheet 4 and the non-breathable resin sheet 4 and the porous mat 5, it is not necessary to consider the breathability, so that it is limited to the breathable adhesive. A well-known bonding method can be applied.
In the present invention, the breathable outer covering material 2, the paper material 1, and the moldable felt 3 may be joined by a method other than adhesion, such as welding or fusion.
〔内装材成形物〕
上記内装材6は、例えば自動車の床形状に適合する所定形状に成形される。上記内装材6の構成要素である通気性表装材2、紙材料1、または成形性フェルト3に熱可塑性樹脂が塗布および/または含浸および/または混合されているか、あるいは上記通気性表装材2、または成形性フェルト3が低融点熱可塑性樹脂繊維からなるか、あるいは低融点熱可塑性樹脂繊維を含む場合に上記内装材6を成形するには、上記内装材6を上記熱可塑性樹脂あるいは低融点熱可塑性樹脂繊維の軟化温度以下でホットプレスを行なうか、あるいは上記軟化温度以上に加熱した上でコールドプレスを行なう。また、これらに熱硬化性樹脂が塗布されている場合は、ホットプレスで成形してもよい。
[Interior material moldings]
The interior material 6 is formed into a predetermined shape that conforms to the floor shape of an automobile, for example. A thermoplastic resin is applied and / or impregnated and / or mixed with the breathable outer covering material 2, the paper material 1, or the moldable felt 3, which is a component of the interior material 6, or the breathable outer covering material 2, Alternatively, when the formable felt 3 is made of low-melting point thermoplastic resin fibers or contains low-melting point thermoplastic resin fibers, in order to form the interior material 6, the interior material 6 is made of the thermoplastic resin or low-melting point heat. Hot pressing is performed at a temperature equal to or lower than the softening temperature of the plastic resin fiber, or cold pressing is performed after heating at a temperature equal to or higher than the softening temperature. Moreover, when a thermosetting resin is applied to these, it may be molded by hot pressing.
以下に本発明を更に具体的に説明するための実施例を記載するが、本発明は該実施例にのみ限定されるものではない。 Examples for describing the present invention more specifically will be described below, but the present invention is not limited to these examples.
〔実施例1〕
ポリエステル繊維からなる目付量120g/m2、厚さ3mmのニードルパンチング不織布である通気性表装材を作製した。
次に、針葉樹パルプ50質量部および広葉樹パルプ50質量部からなる木材パルプを原料とし、ディスクリファイナーを用いて叩解度がJIS P 8121−1995の4.カナディアン・スタンダード・フリーネスに規定されるカナダ標準型ろ水度で490ml(CSF)になるように叩解し、通常の抄紙工程を経てクレープ率25%、目付量30g/m2、通気抵抗0.84kPa・s/mの多孔質パルプ繊維からなる紙材料を作製した。
上記紙材料の片面にポリエステル樹脂からなる融点150℃、粒度200〜300μmのホットメルト接着剤粉末を3g/m2の撒布量で塗布した後、塗布面に上記通気性表装材を積層し、180℃の加熱ロールにて紙材料側から軽く圧着して上記通気性表装材に紙材料を裏打ちした。
上記積層物に紙材料側からポリエステル樹脂からなる融点120℃、粒度200〜300μmのホットメルト接着剤粉末を3g/m2の撒布量で塗布し、140℃に加熱しホットメルト接着剤を紙材料に融着させた。このものの通気抵抗は1.23kPa・s/mであった。
次に、低融点ポリエステル繊維(繊度:2.2dtex、融点:120℃)を30質量部、通常ポリエステル繊維(繊度:6.6dtex)70質量部からなる繊維ウェブを180℃で吸引しながら加熱することで上記低融点ポリエステル繊維を溶融して通常ポリエステル繊維と接着させ、目付量300g/m2、厚さ15mm、通気抵抗0.06kPa・s/mの成形性フェルトを作製した。
更に、ポリアミド樹脂(厚さ:0.2mm、目付量:100g/m2、軟化点:120℃)のシートである非通気性樹脂シートを作製した。
また更に、上記成形性フェルトと同配合による厚さ10mm、目付量800g/m2のフェルトシートである多孔質マットを作製した。
なお、このとき上記紙材料を裏打ちした通気性表装材の紙材料側に上記多孔質マットを積層し、180℃で加熱した後、直ちに冷却して(通気性表装材−紙材料)−成形性フェルトの順に積層接着したものの通気抵抗は1.29kPa・s/mであった。
次に、上記で得られた各材料を、(通気性表装材―紙材料)−成形性フェルト−非通気性樹脂シート−多孔質マットの順に積層し(紙材料が通気性表装材と成形性フェルトに挟まれる形となる)、180℃で加熱した後、直ちに冷却し、厚さ26.0mm、重さ1356g/m2の内装材(No.1)を作製した。
[Example 1]
A breathable outer covering material which is a needle punching nonwoven fabric having a basis weight of 120 g / m 2 and a thickness of 3 mm made of polyester fiber was prepared.
Next, a wood pulp composed of 50 parts by mass of softwood pulp and 50 parts by mass of hardwood pulp is used as a raw material, and the degree of beating is 4 according to JIS P 8121-1995 using a disc refiner. It is beaten to a Canadian standard freeness of 490 ml (CSF) as specified by Canadian Standard Freeness, and after a normal paper making process, the crepe rate is 25%, the basis weight is 30 g / m 2 , and the ventilation resistance is 0.84 kPa. A paper material made of s / m porous pulp fibers was prepared.
A hot melt adhesive powder made of polyester resin having a melting point of 150 ° C. and a particle size of 200 to 300 μm was applied on one side of the paper material in a spreading amount of 3 g / m 2 , and then the breathable surface material was laminated on the coated surface. The paper material was lined on the breathable outer covering material by lightly pressing from the paper material side with a heating roll at 0 ° C.
From the paper material side, a hot melt adhesive powder having a melting point of 120 ° C. and a particle size of 200 to 300 μm is applied to the laminate with a spreading amount of 3 g / m 2 and heated to 140 ° C. to apply the hot melt adhesive to the paper material. Fused. The ventilation resistance of this product was 1.23 kPa · s / m.
Next, a fiber web consisting of 30 parts by mass of low-melting polyester fibers (fineness: 2.2 dtex, melting point: 120 ° C.) and 70 parts by mass of normal polyester fibers (fineness: 6.6 dtex) is heated while being sucked at 180 ° C. Thus, the low-melting-point polyester fiber was melted and adhered to the normal polyester fiber to produce a moldable felt having a basis weight of 300 g / m 2 , a thickness of 15 mm, and a ventilation resistance of 0.06 kPa · s / m.
Furthermore, a non-breathable resin sheet which was a sheet of polyamide resin (thickness: 0.2 mm, basis weight: 100 g / m 2 , softening point: 120 ° C.) was produced.
Furthermore, a porous mat, which is a felt sheet having a thickness of 10 mm and a weight per unit area of 800 g / m 2 by the same composition as the moldable felt, was prepared.
At this time, the porous mat is laminated on the paper material side of the breathable covering material lined with the paper material, heated at 180 ° C., and then immediately cooled (breathable covering material-paper material) -formability. The airflow resistance of the laminates laminated in the order of felt was 1.29 kPa · s / m.
Next, each material obtained above is laminated in the order of (breathable outer covering material−paper material) −moldable felt−non-breathable resin sheet−porous mat (the paper material is made of the breathable outer covering material and the moldability). After being heated at 180 ° C. and immediately cooled, an interior material (No. 1) having a thickness of 26.0 mm and a weight of 1356 g / m 2 was produced.
〔実施例2〕
実施例1において、成形性フェルトの目付量を150g/m2とした他は同様にして厚さ26.0mm、重さ1206g/m2の内装材(No.2)を作製した。
なお、このときの成形性フェルトの通気抵抗は0.04kPa・s/mであり、実施例1と同様に(通気性表装材−紙材料)−成形性フェルトの順に積層し、加熱−冷却し積層接着したものの通気抵抗は1.27kPa・s/mであった。
[Example 2]
An interior material (No. 2) having a thickness of 26.0 mm and a weight of 1206 g / m 2 was produced in the same manner as in Example 1, except that the basis weight of the moldable felt was 150 g / m 2 .
In addition, the ventilation resistance of the moldable felt at this time is 0.04 kPa · s / m, and in the same manner as in Example 1, (breathable outer covering material−paper material) −moldable felt are laminated in this order, and heated and cooled. The airflow resistance of the laminated adhesive was 1.27 kPa · s / m.
〔実施例3〕
実施例1において、成形性フェルトの目付量を100g/m2とした他は同様にして厚さ26.0mm、重さ1156g/m2の内装材(No.3)を作製した。
なお、このときの成形性フェルトの通気抵抗は0.03kPa・s/mであり、実施例1と同様に(通気性表装材−紙材料)−成形性フェルトの順に積層し、加熱−冷却し積層接着したものの通気抵抗は1.26kPa・s/mであった。
Example 3
An interior material (No. 3) having a thickness of 26.0 mm and a weight of 1156 g / m 2 was produced in the same manner as in Example 1, except that the basis weight of the moldable felt was 100 g / m 2 .
In addition, the ventilation resistance of the moldable felt at this time is 0.03 kPa · s / m. Similarly to Example 1, (breathable outer cover material−paper material) −moldable felt are laminated in this order, and heated and cooled. The airflow resistance of the laminated adhesive was 1.26 kPa · s / m.
〔実施例4〕
実施例1において、成形性フェルトの厚さを10mmとした他は同様にして厚さ20.0mm、重さ1356g/m2の内装材(No.4)を作製した。
なお、このときの成形性フェルトの通気抵抗は0.07kPa・s/mであり、実施例1と同様に(通気性表装材−紙材料)−成形性フェルトの順に積層し、加熱−冷却し積層接着したものの通気抵抗は1.30kPa・s/mであった。
Example 4
An interior material (No. 4) having a thickness of 20.0 mm and a weight of 1356 g / m 2 was produced in the same manner as in Example 1, except that the thickness of the moldable felt was 10 mm.
In addition, the ventilation resistance of the moldable felt at this time is 0.07 kPa · s / m, and in the same manner as in Example 1, (air-permeable outer covering material−paper material) −moldable felt are laminated in this order, and heated and cooled. The ventilation resistance of the laminated adhesive was 1.30 kPa · s / m.
〔実施例5〕
実施例1において、非通気性樹脂シートをポリアミド樹脂(厚さ:1.0mm、目付量:500g/m2)のシートを使用した他は同様にして、厚さ26.0mm、重さ1756g/m2の内装材(No.5)を作製した。
Example 5
In Example 1, a non-breathable resin sheet was used in the same manner except that a polyamide resin sheet (thickness: 1.0 mm, basis weight: 500 g / m 2 ) was used, and the thickness was 26.0 mm and the weight was 1756 g / An interior material (No. 5) of m 2 was produced.
〔比較例1〕
実施例1において、紙材料(紙材料の両面に用いたホットメルト接着剤も含める)の代わりに、ポリアミド樹脂(厚さ:0.2mm、目付量:60g/m2、軟化点:120℃)からなるシートに加熱した針にて貫通孔(直径:約0.9〜1.0mm、孔数:130個/100mm×100mm)を設けた開孔樹脂層を使用した他は同様にして、通気性表装材−開孔樹脂層−成形性フェルト−非通気性樹脂シート−多孔質マットからなる厚さ26.0mm、重さ1380g/m2の内装材(No.6)を作製した。
なお、このときの開孔樹脂層の通気抵抗は1.17kPa・s/mであり、実施例1と同様に通気性表装材−開孔樹脂層−成形性フェルトの順に積層し、加熱−冷却し積層接着したものの通気抵抗は1.28kPa・s/mであった。
[Comparative Example 1]
In Example 1, instead of paper material (including hot-melt adhesive used on both sides of the paper material), polyamide resin (thickness: 0.2 mm, basis weight: 60 g / m 2 , softening point: 120 ° C.) Ventilation was performed in the same manner except that an apertured resin layer having through holes (diameter: about 0.9 to 1.0 mm, number of holes: 130/100 mm × 100 mm) was used with a heated needle on the sheet made of An interior material (No. 6) having a thickness of 26.0 mm and a weight of 1380 g / m 2 made of a surface covering material, an apertured resin layer, a moldable felt, a non-breathable resin sheet, and a porous mat was produced.
In addition, the ventilation resistance of the apertured resin layer at this time is 1.17 kPa · s / m, and in the same manner as in Example 1, the breathable outer covering material, the apertured resin layer, and the moldable felt are laminated in this order, and heating-cooling is performed. The air flow resistance of the laminated and bonded materials was 1.28 kPa · s / m.
〔比較例2〕
比較例1において、成形性フェルトの目付量を150g/m2とした他は同様にして厚さ26.0mm、重さ1230g/m2の内装材(No.7)を作製した。
なお、このときの成形性フェルトの通気抵抗は0.04g/m2であり、比較例1と同様に通気性表装材−開孔樹脂層−成形性フェルトの順に積層し、加熱−冷却し積層接着したものの通気抵抗は1.27kPa・s/mであった。
[Comparative Example 2]
In Comparative Example 1, an interior material (No. 7) having a thickness of 26.0 mm and a weight of 1230 g / m 2 was produced in the same manner except that the weight of the moldable felt was 150 g / m 2 .
In addition, the ventilation resistance of the moldable felt at this time is 0.04 g / m 2 , and in the same manner as in Comparative Example 1, the breathable outer covering material, the aperture resin layer, and the moldable felt are laminated in this order, and heated and cooled to laminate. The gas flow resistance of the bonded material was 1.27 kPa · s / m.
〔比較例3〕
比較例1において、成形性フェルトの目付量を100g/m2とした他は同様にして厚さ26.0mm、重さ1180g/m2の内装材(No.8)を作製した。
なお、このときの成形性フェルトの通気抵抗は0.03g/m2であり、比較例1と同様に通気性表装材−開孔樹脂層−成形性フェルトの順に積層し、加熱−冷却し積層接着したものの通気抵抗は1.25kPa・s/mであった。
[Comparative Example 3]
In Comparative Example 1, an interior material (No. 8) having a thickness of 26.0 mm and a weight of 1180 g / m 2 was produced in the same manner except that the basis weight of the moldable felt was 100 g / m 2 .
In addition, the ventilation resistance of the moldable felt at this time is 0.03 g / m 2 , and in the same manner as in Comparative Example 1, the breathable outer covering material, the apertured resin layer, and the moldable felt are stacked in this order, heated and cooled, and stacked. The gas flow resistance of the bonded material was 1.25 kPa · s / m.
〔比較例4〕
比較例1において、成形性フェルトの厚さを10mmとした他は同様にして厚さ20.0mm、重さ1380g/m2の内装材(No.9)を作製した。
なお、このときの成形性フェルトの通気抵抗は0.07g/m2であり、比較例1と同様に通気性表装材−開孔樹脂層−成形性フェルトの順に積層し、加熱−冷却し積層接着したものの通気抵抗は1.29kPa・s/mであった。
[Comparative Example 4]
In Comparative Example 1, an interior material (No. 9) having a thickness of 20.0 mm and a weight of 1380 g / m 2 was produced in the same manner except that the thickness of the moldable felt was 10 mm.
In addition, the ventilation resistance of the moldable felt at this time is 0.07 g / m 2 , and in the same manner as in Comparative Example 1, the breathable outer covering material, the apertured resin layer, and the moldable felt are laminated in this order, heated and cooled, and laminated. The gas flow resistance of the bonded material was 1.29 kPa · s / m.
〔比較例5〕
比較例1において、非通気性樹脂シートをポリアミド樹脂(厚さ:1.0mm、目付量:500g/m2)のシートを使用した他は同様にして、厚さ26.0mm、重さ1780g/m2の内装材(No.10)を作製した。
[Comparative Example 5]
In Comparative Example 1, a non-breathable resin sheet was used in the same manner except that a polyamide resin sheet (thickness: 1.0 mm, basis weight: 500 g / m 2 ) was used, and the thickness was 26.0 mm and the weight was 1780 g / An interior material (No. 10) of m 2 was produced.
上記実施例1〜4および比較例1〜4で得られた内装材No.1〜8の吸音性試験をJIS A 1409「残響室法吸音率」に準じて測定した結果を表1に示す。
また、上記実施例1、実施例5および比較例1、比較例5で得られた内装材No.1、No.5、No.6、No.10の遮音性試験をJIS A 1416「音響透過損失」に準じて測定した結果を表2に示す。
The interior material Nos. Obtained in Examples 1 to 4 and Comparative Examples 1 to 4 were used. Table 1 shows the results of measuring the sound absorption test of 1 to 8 according to JIS A 1409 “Reverberation chamber method sound absorption coefficient”.
In addition, the interior material Nos. Obtained in Example 1, Example 5, Comparative Example 1, and Comparative Example 5 were used. 1, no. 5, no. 6, no. Table 2 shows the results obtained by measuring 10 sound insulation tests according to JIS A 1416 “Sound transmission loss”.
表1より、成形性フェルトの目付量(質量)を300g/m2から150g/m2、そして100g/m2まで減じたところ、本実施例1〜3における内装材No.1、No.2、No.3については吸音率の低下が殆んど見られなかったが、紙材料に代えて開孔樹脂層を使用した比較例1〜3における内装材No.6、No.7、No.8については、成形性フェルトの質量の減少に伴って吸音率の低下が顕著であることが判る。
また、成形性フェルトの厚みだけを15mmから10mmに変化させたところ、本実施例1,4における内装材No.1とNo.4を比べてみると吸音率にあまり変化が見られないが、比較例1,4における内装材No.6とNo.9をみると、成形性フェルトの厚さを15mmから10mmと薄くすることで大きく吸音率が低下していることが判る。
上記結果より、本発明による表面に開口する多数の細孔からなる多孔質パルプ繊維を用いた紙材料を使用することで、通気抵抗が同程度であれば、最終的な製品の軽量化や厚さの低減が可能になることが判る。更に、成形性フェルトやその他の材料の厚さ、密度、通気抵抗によらず、紙材料の通気抵抗を調整することで簡単に性能を向上させることができることになる。
From Table 1, where the basis weight of the moldability felt (mass) was subtracted from 300g / m 2 150g / m 2 and up to 100 g / m 2,, interior material of the present embodiment 1 to 3 No. 1, no. 2, No. Although almost no decrease in the sound absorption coefficient was observed for No. 3, the interior material Nos. 1 to 3 in Comparative Examples 1 to 3 using an apertured resin layer instead of the paper material were used. 6, no. 7, no. For No. 8, it can be seen that the decrease in the sound absorption coefficient is remarkable with the decrease in the mass of the moldable felt.
Further, when only the thickness of the moldable felt was changed from 15 mm to 10 mm, the interior material No. 1 and No. 4 does not change much in the sound absorption coefficient, but the interior material No. 6 and no. 9 shows that the sound absorption coefficient is greatly reduced by reducing the thickness of the moldable felt from 15 mm to 10 mm.
From the above results, by using a paper material using porous pulp fibers consisting of a large number of pores opening on the surface according to the present invention, if the airflow resistance is about the same, the final product can be reduced in weight and thickness. It can be seen that this can be reduced. Further, the performance can be easily improved by adjusting the airflow resistance of the paper material regardless of the thickness, density, and airflow resistance of the formable felt and other materials.
表2より、遮音性においては、紙材料と開孔樹脂層との間に差は殆んど見られず、非通気性樹脂シートの目付量(質量)が増えるほど遮音性能が向上する。
これらの事より、本実施例における内装材を自動車の内装材料として使用する場合は、車体側に多孔質マット側がくるように配置し、通気性表装材側が車内にくるように配置すると、車外からの騒音を遮音し、更に洩れてきた騒音を室内で吸音することが出来、この場合に従来の開孔樹脂層を設けた吸音材よりも軽量で厚みを小さくすることが可能となる。
From Table 2, in sound insulation, there is almost no difference between the paper material and the aperture resin layer, and the sound insulation performance improves as the basis weight (mass) of the non-breathable resin sheet increases.
From these things, when using the interior material in this embodiment as the interior material of an automobile, it is arranged so that the porous mat side comes to the vehicle body side, and the breathable surface material side comes to the inside of the vehicle. In addition, the leaked noise can be absorbed indoors. In this case, it is possible to reduce the thickness and reduce the thickness of the sound absorbing material provided with the conventional aperture resin layer.
〔実施例6〕
ポリエステル繊維からなる目付量80g/m2、厚さ2mmのニードルパンチング不織布である通気性表装材を作製した。
次に、針葉樹パルプからなる木材パルプを原料とし、ディスクリファイナーを用いて叩解度がJIS P 8121−1995の4.カナディアン・スタンダード・フリーネスに規定されるカナダ標準型ろ水度で420ml(CSF)になるように叩解し、通常の抄紙工程を経てクレープ率20%、目付量20g/m2、通気抵抗1.14kPa・s/mの多孔質パルプ繊維からなる紙材料を作製した。
上記紙材料の片面にポリエステル樹脂からなる融点150℃、粒度200〜300μmのホットメルト接着剤粉末を3g/m2の撒布量で塗布した後、塗布面に上記通気性表装材を積層し、180℃の加熱ロールにて紙材料側から軽く圧着して上記通気性表装材に紙材料を裏打ちした。
上記積層物にフェノール−アルキルレゾルシン初期縮合物(固形分:40質量%水溶液)20質量部、リン−窒素系難燃剤(固形分:40質量%水溶液)5質量部、カーボンブラック(固形分:20質量%水分散液)2質量部、水73質量部からなる混合溶液を固形分として20g/m2の含浸量になるようにロールにて塗布した後、140℃にて5分間加熱し、熱硬化性樹脂をB状態にした。このものの通気抵抗は1.21kPa・s/mであった。
次に、ケナフ繊維30質量部、通常ポリエステル繊維(繊度:6.6dtex)70質量部からなる繊維ウェブに上記混合溶液を固形分で50g/m2の塗布量になるようにスプレー塗布し、180℃に加熱して熱硬化性樹脂をB状態にした目付量200g/m2、厚さ20mm、通気抵抗0.16kPa・s/mである成形性フェルトを作製した。
非通気性樹脂シートとしては、実施例1と同じ非通気性樹脂シートを用いた。
更に、目付量180g/m2、厚さ20mmのメラミン発泡体である多孔質マットを作製した。
次に、上記で得られた各材料を、(通気性表装材―紙材料)−成形性フェルト−非通気性樹脂シート−多孔質マットの順に積層し(紙材料が通気性表装材と成形性フェルトに挟まれる形となる)、200℃で加熱プレス成形し所定形状の内装材を作製した。得られた内装材は総重量が653g/m2と軽量であり、難燃性、吸音性および遮音性に優れた成形物であった。
Example 6
A breathable surface covering material, which is a needle punching nonwoven fabric having a basis weight of 80 g / m 2 and a thickness of 2 mm, made of polyester fiber was produced.
Next, using wood pulp made of softwood pulp as a raw material, the degree of beating is 4 according to JIS P 8121-1995 using a disc refiner. It is beaten to a Canadian standard freeness of 420 ml (CSF) as specified by Canadian Standard Freeness, and after a normal paper making process, the crepe rate is 20%, the basis weight is 20 g / m 2 , and the ventilation resistance is 1.14 kPa. A paper material made of s / m porous pulp fibers was prepared.
A hot melt adhesive powder made of polyester resin having a melting point of 150 ° C. and a particle size of 200 to 300 μm was applied on one side of the paper material in a spreading amount of 3 g / m 2 , and then the breathable surface material was laminated on the coated surface. The paper material was lined on the breathable outer covering material by lightly pressing from the paper material side with a heating roll at 0 ° C.
20 parts by mass of a phenol-alkylresorcin initial condensate (solid content: 40% by mass aqueous solution), 5 parts by mass of a phosphorus-nitrogen flame retardant (solid content: 40% by mass aqueous solution), carbon black (solid content: 20) (Mass% aqueous dispersion) A mixed solution consisting of 2 parts by mass and 73 parts by mass of water was applied as a solid so as to have an impregnation amount of 20 g / m 2 and then heated at 140 ° C. for 5 minutes, The curable resin was in the B state. The ventilation resistance of this product was 1.21 kPa · s / m.
Next, the above mixed solution is spray-coated on a fiber web composed of 30 parts by mass of kenaf fibers and 70 parts by mass of normal polyester fibers (fineness: 6.6 dtex) so as to have an application amount of 50 g / m 2 in terms of solid content. A moldable felt having a weight per unit area of 200 g / m 2 , a thickness of 20 mm, and a ventilation resistance of 0.16 kPa · s / m was produced by heating to 0 ° C. to bring the thermosetting resin into a B state.
As the non-breathable resin sheet, the same non-breathable resin sheet as in Example 1 was used.
Furthermore, a porous mat which is a melamine foam having a basis weight of 180 g / m 2 and a thickness of 20 mm was produced.
Next, each material obtained above is laminated in the order of (breathable outer covering material−paper material) −moldable felt−non-breathable resin sheet−porous mat (the paper material is made of the breathable outer covering material and the moldability). The inner material having a predetermined shape was manufactured by hot press molding at 200 ° C. The obtained interior material was lightweight with a total weight of 653 g / m 2 and was a molded product excellent in flame retardancy, sound absorption and sound insulation.
〔実施例7〕
実施例6において、積層物および成形性フェルトの樹脂含浸に用いた混合溶液中のフェノール−アルキルレゾルシン初期縮合物(固形分:40質量%水溶液)を、アクロデュア958D(固形分:42質量%水性エマルジョン)に代え、他の成分は同様にして積層物および成形性フェルトを作製した。上記積層物の通気抵抗は1.34kPa・s/mであり、成形性フェルトは目付量200g/m2、厚さ20mm、通気抵抗0.18kPa・s/mであった。
上記積層物および成形性フェルトを用いて実施例6と同様に200℃で加熱プレス成形し所定形状の内装材を作製した。得られた内装材は軽量で吸音性、遮音性に優れた成形物であった。
Example 7
In Example 6, the phenol-alkylresorcin initial condensate (solid content: 40% by mass aqueous solution) in the mixed solution used for resin impregnation of the laminate and the moldable felt was converted to Acrodure 958D (solid content: 42% by mass aqueous emulsion). In the same manner as above, other components were used to produce laminates and moldable felts. The laminate had a ventilation resistance of 1.34 kPa · s / m, a moldable felt having a basis weight of 200 g / m 2 , a thickness of 20 mm, and a ventilation resistance of 0.18 kPa · s / m.
Using the laminate and the moldable felt, heat press molding was performed at 200 ° C. in the same manner as in Example 6 to prepare an interior material having a predetermined shape. The obtained interior material was lightweight and was a molded product excellent in sound absorption and sound insulation.
〔実施例8〕
実施例6において、積層物および成形性フェルトの樹脂含浸に用いた混合溶液中のフェノール−アルキルレゾルシン初期縮合物(固形分:40質量%水溶液)を、アクロデュア950L(固形分:50質量%水溶液)とアクロデュア958D(固形分:42質量%水性エマルジョン)の50:50質量比混合溶液に代え、他の成分は同様にして積層物および成形性フェルトを作製した。上記積層物の通気抵抗は1.26kPa・s/mであり、成形性フェルトは目付量200g/m2、厚さ20mm、通気抵抗0.23kPa・s/mであった。
上記積層物および成形性フェルトを用いて実施例6と同様に200℃で加熱プレス成形し所定形状の内装材を作製した。得られた内装材は軽量で吸音性、遮音性に優れた成形物であった。
Example 8
In Example 6, the phenol-alkylresorcin initial condensate (solid content: 40 mass% aqueous solution) in the mixed solution used for resin impregnation of the laminate and the moldable felt was added to Acrodure 950 L (solid content: 50 mass% aqueous solution). Acrodea 958D (solid content: 42 mass% aqueous emulsion) was replaced with a 50:50 mass ratio mixed solution, and other components were similarly produced to produce laminates and moldable felts. The laminate had a ventilation resistance of 1.26 kPa · s / m, a moldable felt having a basis weight of 200 g / m 2 , a thickness of 20 mm, and a ventilation resistance of 0.23 kPa · s / m.
Using the laminate and the moldable felt, heat press molding was performed at 200 ° C. in the same manner as in Example 6 to prepare an interior material having a predetermined shape. The obtained interior material was lightweight and was a molded product excellent in sound absorption and sound insulation.
〔比較例6〕
上記実施例1において、紙材料を省略した以外は同様にして、通気性表装材−成形性フェルト−非通気性樹脂シート−多孔質マットの順に積層し、180℃で加熱した後、直ちに冷圧プレス成形し所定形状の内装材を作製した。得られた内装材は実施例1に比べて吸音性に乏しく、自動車用内装材として使用するには不適であった。
[Comparative Example 6]
In Example 1 above, except that the paper material was omitted, in the same manner, the breathable outer covering material-moldable felt-non-breathable resin sheet-porous mat were laminated in this order, heated at 180 ° C., and then immediately cooled. An interior material having a predetermined shape was produced by press molding. The obtained interior material was poor in sound absorption as compared with Example 1, and was unsuitable for use as an automotive interior material.
本発明の内装材6は、良好な吸音性能、遮音性能を有し、更に軽量であり、従来の材料よりも厚みを薄くすることができるので、産業上利用可能である。 The interior material 6 of the present invention has good sound absorption performance and sound insulation performance, is lighter in weight, and can be made thinner than conventional materials, so that it can be used industrially.
1 紙材料
1a エンボス加工紙(延伸性紙材料)
2 通気性表装材
3 成形性フェルト
4 非通気性樹脂シート
5 多孔質マット
6 自動車用内装材
R 通気抵抗
1 Paper material 1a Embossed paper (extensible paper material)
2 Breathable surface material 3 Moldable felt 4 Non-breathable resin sheet 5 Porous mat 6 Automotive interior material R Ventilation resistance
Claims (4)
上記紙材料は叩解度がJIS P 8121−1995の4.カナディアン・スタンダード・フリーネスに規定されるカナダ標準型ろ水度で350〜650ml(CSF)の範囲であり表面に開口する多数の細孔が設けられている多孔質パルプ繊維を90質量%以上含み、通気抵抗が0.07〜3.00kPa・s/mの範囲の紙である
ことを特徴とする自動車用内装材。For automobiles in which a non-breathable resin sheet is laminated on a porous mat, a moldable felt is laminated on the non-breathable resin sheet, and a breathable surface material lined with a paper material is laminated on the moldable felt Interior material,
The paper material has a beating degree of JIS P 8121-1995. 90% by mass or more of a porous pulp fiber having a Canadian standard freeness prescribed by Canadian Standard Freeness in the range of 350 to 650 ml (CSF) and having a large number of pores opened on the surface, An interior material for automobiles, wherein the ventilation resistance is paper having a range of 0.07 to 3.00 kPa · s / m.
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PCT/JP2010/057810 WO2011045950A1 (en) | 2009-10-13 | 2010-05-07 | Interior material for motor vehicles |
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JPWO2011045950A1 (en) | 2013-03-04 |
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