JP6584908B2 - Spunbond nonwoven fabric with flexibility - Google Patents
Spunbond nonwoven fabric with flexibility Download PDFInfo
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- JP6584908B2 JP6584908B2 JP2015203921A JP2015203921A JP6584908B2 JP 6584908 B2 JP6584908 B2 JP 6584908B2 JP 2015203921 A JP2015203921 A JP 2015203921A JP 2015203921 A JP2015203921 A JP 2015203921A JP 6584908 B2 JP6584908 B2 JP 6584908B2
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- nonwoven fabric
- carbon dioxide
- resin
- dioxide generation
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- 239000004745 nonwoven fabric Substances 0.000 title claims description 107
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 188
- 239000001569 carbon dioxide Substances 0.000 claims description 94
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 94
- 239000003112 inhibitor Substances 0.000 claims description 65
- 239000002245 particle Substances 0.000 claims description 45
- 229920005989 resin Polymers 0.000 claims description 34
- 239000011347 resin Substances 0.000 claims description 34
- 239000000835 fiber Substances 0.000 claims description 32
- 239000000463 material Substances 0.000 claims description 19
- 229920001225 polyester resin Polymers 0.000 claims description 17
- -1 polyethylene terephthalate Polymers 0.000 claims description 15
- 239000004645 polyester resin Substances 0.000 claims description 11
- 229920002292 Nylon 6 Polymers 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 239000002184 metal Substances 0.000 claims description 10
- 229920002647 polyamide Polymers 0.000 claims description 10
- 229920006122 polyamide resin Polymers 0.000 claims description 9
- 239000006185 dispersion Substances 0.000 claims description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 8
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 8
- 238000010276 construction Methods 0.000 claims description 7
- 229920002302 Nylon 6,6 Polymers 0.000 claims description 5
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 5
- 239000000395 magnesium oxide Substances 0.000 claims description 5
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 5
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 5
- 229920000728 polyester Polymers 0.000 claims description 5
- 229920001707 polybutylene terephthalate Polymers 0.000 claims description 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 150000002632 lipids Chemical class 0.000 claims description 3
- 239000005022 packaging material Substances 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical class O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 2
- 229910000503 Na-aluminosilicate Inorganic materials 0.000 description 32
- 239000000429 sodium aluminium silicate Substances 0.000 description 32
- 235000012217 sodium aluminium silicate Nutrition 0.000 description 32
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 32
- 238000009987 spinning Methods 0.000 description 21
- 230000000052 comparative effect Effects 0.000 description 20
- 238000000034 method Methods 0.000 description 20
- 238000002844 melting Methods 0.000 description 16
- 230000008018 melting Effects 0.000 description 16
- 230000000694 effects Effects 0.000 description 11
- 230000002776 aggregation Effects 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 230000001629 suppression Effects 0.000 description 7
- 238000004220 aggregation Methods 0.000 description 6
- 238000002485 combustion reaction Methods 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 5
- 238000007380 fibre production Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 238000004049 embossing Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 3
- 229910002113 barium titanate Inorganic materials 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000002788 crimping Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 description 2
- 150000004692 metal hydroxides Chemical class 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920001169 thermoplastic Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- 229920003189 Nylon 4,6 Polymers 0.000 description 1
- 229920000007 Nylon MXD6 Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000012773 agricultural material Substances 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
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 229920006167 biodegradable resin Polymers 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000004566 building material Substances 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
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000003484 crystal nucleating agent Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000005003 food packaging material Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 239000012771 household material Substances 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000002502 liposome Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 229910052912 lithium silicate Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 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
- 239000012528 membrane Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002215 polytrimethylene terephthalate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Protection Of Plants (AREA)
- Nonwoven Fabrics (AREA)
Description
本発明は、土木、建築、農業、産業、生活資材等の資材用途に適した燃焼時二酸化炭素発生量を抑制するスパンボンド不織布に関する。 The present invention relates to a spunbonded nonwoven fabric that suppresses the amount of carbon dioxide generated during combustion, which is suitable for materials such as civil engineering, architecture, agriculture, industry, and daily life.
スパンボンド不織布は、布強度が強く、低コストで生産性が高いため、土木、建築、農業、産業、生活資材を中心に広範な用途で使用されている一方で、大量に普及したことから廃棄時の焼却処分における有害物質発生等の環境問題を引き起こしている。その中で地球温暖化への影響から排出量削減が強く望まれている二酸化炭素は燃焼の最終生成物であることから削減が難しいのが現状である。 Spunbond nonwoven fabrics are strong in fabric strength, low in cost and high in productivity, so they are used in a wide range of applications mainly in civil engineering, construction, agriculture, industry, and living materials, but discarded because they have spread in large quantities. Causing environmental problems such as the generation of hazardous substances during incineration. Among them, the current situation is that it is difficult to reduce carbon dioxide, which is strongly desired to reduce emissions due to its impact on global warming, because it is the final product of combustion.
他方、この焼却への対策として、埋め立てによって自然分解する生分解性樹脂も存在するが、大量に使用されるスパンボンド不織布を置き換え、全て埋め立てによって処分することは困難である為、廃棄方法は焼却が重要な位置を占めているのが現状である。
また、排気量そのものを削減する方法として、再生利用が行われているが、再生利用は未だ一部でしか採用されておらず、再利用を重ねるごとに強度等の物性が落ち、最終的に焼却されることとなるため、二酸化炭素排出の根本的な解決とはならない。以上の様な二酸化炭素排出問題を解決するため、二酸化炭素量を抑制する化合物を樹脂に配合する方法（例えば、特許文献１、２参照）が提案されている。
On the other hand, as a countermeasure against this incineration, there is a biodegradable resin that is naturally decomposed by landfill, but it is difficult to replace a large amount of spunbond nonwoven fabric and dispose of it by landfill. Currently occupies an important position.
In addition, recycling is used as a method to reduce the exhaust amount itself, but recycling is still used only partially, and physical properties such as strength decrease each time reuse is repeated. Since it will be incinerated, it will not be a fundamental solution to carbon dioxide emissions. In order to solve the carbon dioxide emission problem as described above, a method of blending a compound that suppresses the amount of carbon dioxide with a resin (see, for example, Patent Documents 1 and 2) has been proposed.
特許文献１や２では、二酸化炭素の発生を抑制する化合物を樹脂に添加して製造したポリエチレンフィルムについての記載がされている。しかし、特許文献１や２に記載している様な添加剤は通常フィルム生産工程で凝集を起こし、ゲル化（フィッシュアイ）や、繊維生産工程では糸切れを発生させる原因となる。特に繊維中における添加剤の凝集は繊維断面積が小さいため、紡糸時の繊維生産工程において曳糸性に顕著に影響する。
また、二酸化炭素発生量抑制剤の様な添加剤を添加すると通常繊維中の結晶配向性は抑制され、繊維・不織布の強度・伸度（タフネス）は低下するものである。また、ボンディング加工を強めることで不織布としての強度を得ることはできるが、タフネスは低下することで不織布の柔軟性は低下する。
Patent Documents 1 and 2 describe a polyethylene film produced by adding a compound that suppresses the generation of carbon dioxide to a resin. However, additives such as those described in Patent Documents 1 and 2 usually cause aggregation in the film production process, and cause gelation (fish eye) and yarn breakage in the fiber production process. In particular, the aggregation of additives in the fiber has a small fiber cross-sectional area, and thus significantly affects the spinnability in the fiber production process during spinning.
Moreover, when an additive such as a carbon dioxide generation amount inhibitor is added, the crystal orientation in the fiber is usually suppressed, and the strength / elongation (toughness) of the fiber / nonwoven fabric is lowered. Moreover, although the intensity | strength as a nonwoven fabric can be acquired by strengthening a bonding process, the softness | flexibility of a nonwoven fabric falls by toughness falling.
本発明が解決しようとする課題は、二酸化炭素発生量抑制剤を、繊維を構成するポリエステル系樹脂又はポリアミド系樹脂中に均一に分散し、かつ、紡糸条件を最適化することにより該繊維の結晶配向性・布の柔軟性を維持し、さらに燃焼時二酸化炭素発生量を抑制したスパンボンド不織布を提供することである。 The problem to be solved by the present invention is that a carbon dioxide generation amount inhibitor is uniformly dispersed in a polyester-based resin or a polyamide-based resin constituting a fiber, and the spinning condition is optimized, thereby crystallizing the fiber. An object of the present invention is to provide a spunbonded nonwoven fabric that maintains orientation and fabric flexibility and further suppresses the amount of carbon dioxide generated during combustion.
本発明の不織布に添加する二酸化炭素発生量抑制剤は、耐熱性が良く、紡糸時に繊維内に直接混練することができ、また、繊維を構成するポリエステル系樹脂又はポリアミド系樹脂中に均一に分散されることで、凝集を引き起こすことがなく、繊維生産工程における曳糸性が良好となり、糸切れが発生することなく高紡速の繊維を得ることができ、強度の強い繊維を形成することが可能となる。更に該二酸化炭素発生量抑制剤は、繊維を構成するポリエステル系樹脂又はポリアミド系樹脂中へ添加しても該繊維の結晶配向性を低下することはなく、逆に紡糸条件を制御することで結晶配向性を向上させることができ、該繊維さらには形成される不織布の強伸度を向上させることができる。柔軟性を有する不織布は生産上の工程安定性や使用時の耐久性が向上したものであるため、土木、建築、農業、産業、生活資材、特に柔軟性が必要とされるカイロ等の包装材料に好適に使用できる。 The carbon dioxide generation amount inhibitor added to the nonwoven fabric of the present invention has good heat resistance, can be kneaded directly into the fiber during spinning, and is uniformly dispersed in the polyester resin or polyamide resin constituting the fiber As a result, agglomeration is not caused, the spinnability in the fiber production process is improved, a high spinning speed fiber can be obtained without causing yarn breakage, and a strong fiber can be formed. It becomes possible. Further, the carbon dioxide generation amount inhibitor does not decrease the crystal orientation of the fiber even when added to the polyester resin or polyamide resin constituting the fiber, and conversely, by controlling the spinning conditions, The orientation can be improved, and the strength and elongation of the nonwoven fabric can be improved. Flexible non-woven fabrics have improved production process stability and durability during use, so civil engineering, architecture, agriculture, industry, life materials, especially packaging materials such as warmers that require flexibility Can be suitably used.
即ち、本発明は下記の通りのものである。
［１］ポリエステル系樹脂又はポリアミド系樹脂から構成されるポリエステル系又はポリアミド系スパンボンド不織布であって、該ポリエステル系樹脂又はポリアミド系樹脂に、粒子径１５０ｎｍ〜２５０ｎｍの二酸化炭素発生量抑制剤が分散され、０．０３〜０．３０重量％で含有されており、かつ、該二酸化炭素発生量抑制剤が、酸化マグネシウム、アルミノケイ酸塩、及びチタン酸化合物からなる群から選ばれる少なくとも１種であることを特徴とする前記不織布。
［２］前記不織布の引張強度が２０〜４００Ｎ／５０ｍｍであり、引張伸度が１０〜７０％であり、かつ、タフネス指数が４０〜３００である、［１］に記載のスパンボンド不織布。
［３］前記不織布を構成する繊維の平均単糸繊度が０．７〜３．０ｄｔｅｘであり、かつ、前記不織布の目付が８〜１００ｇ／ｍ２である、［１］又は［２］に記載のスパンボンド不織布。
［４］前記ポリエステル系樹脂又はポリアミド系樹脂に分散助剤がさらに含有されている、［１］〜［３］のいずれかに記載のスパンボンド不織布。
［５］前記分散助剤が、脂肪酸金属塩、高分子界面活性剤、及び両親媒性脂質から成る群から選ばれる少なくとも１種である、［４］に記載のスパンボンド不織布。
［６］前記ポリエステル系樹脂又はポリアミド系樹脂が、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ナイロン６、及びナイロン６６からなる群から選ばれる少なくとも１種である、［１］〜［５］のいずれかに記載のスパンボンド不織布。
［７］土木、建築、農業、産業又は生活資材用の、［１］〜［６］のいずれかに記載のスパンボンド不織布。
［８］［１］〜［６］のいずれかに記載のスパンボンド不織布を含む包装材料。
That is, the present invention is as follows.
[1] A polyester-based or polyamide-based spunbonded nonwoven fabric composed of a polyester-based resin or a polyamide-based resin, and a carbon dioxide generation amount inhibitor having a particle diameter of 150 nm to 250 nm is dispersed in the polyester-based resin or polyamide-based resin. 0.03 to 0.30% by weight , and the carbon dioxide generation inhibitor is at least one selected from the group consisting of magnesium oxide, aluminosilicates, and titanic acid compounds. The said nonwoven fabric characterized by the above-mentioned.
[2] The spunbonded nonwoven fabric according to [1], wherein the nonwoven fabric has a tensile strength of 20 to 400 N / 50 mm, a tensile elongation of 10 to 70%, and a toughness index of 40 to 300.
[3] The average single yarn fineness of the fibers constituting the nonwoven fabric is 0.7 to 3.0 dtex, and the basis weight of the nonwoven fabric is 8 to 100 g / m 2. Spunbond nonwoven fabric.
[4] The spunbonded nonwoven fabric according to any one of [1] to [3], wherein the polyester resin or polyamide resin further contains a dispersion aid.
[ 5 ] The spunbonded nonwoven fabric according to [ 4 ], wherein the dispersion aid is at least one selected from the group consisting of fatty acid metal salts, polymer surfactants, and amphiphilic lipids.
[ 6 ] The polyester resin or polyamide resin is at least one selected from the group consisting of polyethylene terephthalate, polybutylene terephthalate, nylon 6 and nylon 66, and is described in any one of [1] to [ 5 ]. Spunbond nonwoven fabric.
[ 7 ] The spunbonded nonwoven fabric according to any one of [1] to [ 6 ] for civil engineering, construction, agriculture, industry, or daily life materials.
[ 8 ] A packaging material comprising the spunbonded nonwoven fabric according to any one of [1] to [ 6 ].
通常、繊維を構成する樹脂に添加剤を添加することは、添加剤凝集により、繊維生産工程で糸切れを発生させる原因となるし、また、繊維中の結晶配向性は抑制され、繊維・不織布の強度・伸度（タフネス）も低下する。これに反し、本発明の不織布は、二酸化炭素発生量抑制剤が均一分散されており、タフネス指数が向上され、燃焼時二酸化炭素発生量が抑制され、且つ、強伸度を有し、生産上の工程安定性や使用時の耐久性が向上したものであるため、土木、建築、農業、産業、生活資材として好適に利用可能である。 Usually, adding an additive to the resin constituting the fiber causes the yarn breakage in the fiber production process due to the aggregation of the additive, and the crystal orientation in the fiber is suppressed. The strength / elongation (toughness) is also reduced. On the other hand, the nonwoven fabric of the present invention has a carbon dioxide generation amount inhibitor uniformly dispersed, an improved toughness index, a suppressed carbon dioxide generation amount at the time of combustion, and a high elongation. Therefore, it can be suitably used as civil engineering, construction, agriculture, industry, and daily life materials.
以下、本発明の実施形態について詳述する。
本実施形態の不織布を構成する繊維は、ポリエステル系樹脂及びポリアミド系樹脂からなる群から選ばれる。
Hereinafter, embodiments of the present invention will be described in detail.
The fibers constituting the nonwoven fabric of the present embodiment are selected from the group consisting of polyester resins and polyamide resins.
前記ポリエステル系樹脂としては、熱可塑性ポリエステル、例えば、ポリエチレンテレフタレート、ポリブチレンテレフタレートやポリトリメチレンテレフタレートが代表例として挙げられる。また、熱可塑性ポリエステルは、エステルを形成する酸成分としてイソフタル酸やフタル酸等が重合または共重合されたポリエステルであってもよい。前記ポリエステル系樹脂の何れでも構わない。なかでも、強度、寸法安定性からポリエチレンテレフタレートを選択することが好ましい。 Typical examples of the polyester resin include thermoplastic polyesters such as polyethylene terephthalate, polybutylene terephthalate, and polytrimethylene terephthalate. The thermoplastic polyester may be a polyester obtained by polymerizing or copolymerizing isophthalic acid or phthalic acid as an acid component for forming an ester. Any of the polyester resins may be used. Especially, it is preferable to select polyethylene terephthalate from strength and dimensional stability.
前記ポリアミド系樹脂としては、ナイロン６、ナイロン６６、ナイロン４、ナイロン４６、ナイロン１１、ナイロン１２、ナイロンＭＸＤ６（ポリメタキシレンアジパミド）が挙げられる。前記ポリアミド系樹脂の何れでも構わない。なかでも、強度、寸法安定性からナイロン６又はナイロン６６を選択することが好ましい。
また、前記ポリエステル系樹脂又はポリアミド系樹脂には、他の添加剤、例えば、核剤、難燃剤、無機充填剤、顔料、滑材、着色剤、耐熱安定剤、帯電防止剤、酸化防止剤等を添加してもよい。
Examples of the polyamide-based resin include nylon 6, nylon 66, nylon 4, nylon 46, nylon 11, nylon 12, and nylon MXD6 (polymetaxylene adipamide). Any of the polyamide-based resins may be used. Especially, it is preferable to select nylon 6 or nylon 66 from strength and dimensional stability.
The polyester-based resin or polyamide-based resin includes other additives such as a nucleating agent, a flame retardant, an inorganic filler, a pigment, a lubricant, a colorant, a heat stabilizer, an antistatic agent, an antioxidant, and the like. May be added.
本実施形態のスパンボンド不織布は以下の方法で製造されうる。ポリエステル系樹脂又はポリアミド系樹脂を溶融押出し、多数の紡糸孔を有する紡糸口金から糸条として吐出させる。次いで吐出された糸条を５℃〜２０℃に制御した冷風をあて冷却しながら牽引装置により牽引する。牽引装置より出た糸条を搬送コンベア上に堆積させ不織ウェブとして搬送する。搬送中の不織布ウェブを積層し、多層積層の不織ウェブとしてもよい。目的に応じて、本発明のスパンボンド（Ｓ）不織布をメルトブローン（Ｍ）繊維と積層してもよく、ＳＭ、ＳＭＳ、ＳＭＭＳ、ＳＭＳＭＳと積層した構造であってもよい。 The spunbond nonwoven fabric of this embodiment can be manufactured by the following method. A polyester resin or a polyamide resin is melt-extruded and discharged as a thread from a spinneret having a large number of spinning holes. Next, the discharged yarn is pulled by a pulling device while being cooled by applying cold air controlled at 5 ° C. to 20 ° C. The yarns coming out of the traction device are accumulated on a conveyor and conveyed as a nonwoven web. The nonwoven webs being conveyed may be laminated to form a multilayer laminated nonwoven web. Depending on the purpose, the spunbond (S) nonwoven fabric of the present invention may be laminated with meltblown (M) fibers, or may have a structure laminated with SM, SMS, SMMS, and SMSMS.
紡糸温度は、好ましくは、樹脂の融点より３０℃〜１００℃高く、好ましくは４０℃〜９５℃、より好ましくは４５℃〜７０℃、さらに好ましくは５０℃〜６５℃高い温度である。紡糸温度は融点より１００℃を超えない範囲であれば、樹脂分解物による紡口表面の汚れが少なく、さらに樹脂の粘度が低くなることによる糸切れの発生を抑制することができる。他方、紡糸温度が融点より３０℃を超える範囲であれば、樹脂の粘度が高くなることによる糸切れの発生を抑制し、さらに紡糸時の紡口内圧力が高くなることによる樹脂漏れなどを抑制することができる。
樹脂の融点の測定には、ＳＩＩナノテクノロジー社製のＤＳＣ２１０を使用し、測定雰囲気：窒素ガス５０ｍｌ／ｍｉｎ、昇温速度：１０℃／ｍｉｎ、測定温度範囲：２５〜３００℃の条件下で行い、融解ピークの導入部分における変曲点の漸近線とＴｇより高い温度領域でのベースラインが交わる温度を融点とした。
The spinning temperature is preferably 30 ° C to 100 ° C higher than the melting point of the resin, preferably 40 ° C to 95 ° C, more preferably 45 ° C to 70 ° C, and even more preferably 50 ° C to 65 ° C. If the spinning temperature is within a range not exceeding 100 ° C. from the melting point, it is possible to suppress the occurrence of yarn breakage due to less contamination of the spinneret surface due to the resin decomposition product and lowering of the resin viscosity. On the other hand, if the spinning temperature is in a range exceeding 30 ° C. from the melting point, the occurrence of yarn breakage due to an increase in the viscosity of the resin is suppressed, and further, resin leakage due to an increase in the spinneret pressure during spinning is suppressed. be able to.
For the measurement of the melting point of the resin, DSC210 manufactured by SII NanoTechnology Co., Ltd. is used, and measurement is performed under the conditions of measurement atmosphere: nitrogen gas 50 ml / min, heating rate: 10 ° C./min, measurement temperature range: 25 to 300 ° C. The temperature at which the asymptotic line of the inflection point in the melting peak introduction portion and the baseline in the temperature region higher than Tg intersect was defined as the melting point.
本実施形態のスパンボンド繊維で構成された不織布ウェブを接合して不織布となす場合の接合手段としては、フラットカレンダーロールプレス、エンボスロールプレス等のカレンダー加熱接着方法、その他加熱接着方法では、熱風循環型、熱風貫通型、赤外線ヒーター型、不織布の両面に熱風を吹き付ける方法、あるいは加熱気体中に導入する方法等、各種の加熱する方法が用いられる。また、非加熱方式では、ニードルパンチ法、水流交絡接着等が用いられる。不織ウェブの形態保持や最終的に得られる不織布の強度の観点から、フラットカレンダーロールプレス又はエンボスロールプレスを選択することが好ましい。 In the case of joining the nonwoven web composed of the spunbond fibers of the present embodiment to form a nonwoven fabric, as a joining means, a calender heating adhesive method such as a flat calender roll press and an emboss roll press, and other heat adhering methods, hot air circulation Various heating methods such as a mold, a hot air penetration type, an infrared heater type, a method of blowing hot air on both surfaces of a nonwoven fabric, or a method of introducing into a heated gas are used. In the non-heating method, a needle punch method, hydroentangled adhesion, or the like is used. From the viewpoint of maintaining the shape of the nonwoven web and the strength of the finally obtained nonwoven fabric, it is preferable to select a flat calender roll press or an emboss roll press.
前記フラットカレンダーロールプレスは、金属ロールと金属ロールの組み合わせの一対のロールに通して加工してもよいし、金属ロールと弾性ロールの組み合わせの一対又は二対のロールに通して加工してもよい。表面平滑性の観点では前者金属ロールと金属ロールの組み合わせを選択することが好ましく、不織布の通気性保持の観点では後者を選択することが好ましい。 The flat calender roll press may be processed through a pair of rolls of a combination of a metal roll and a metal roll, or may be processed through a pair of rolls of a combination of a metal roll and an elastic roll. . The combination of the former metal roll and the metal roll is preferably selected from the viewpoint of surface smoothness, and the latter is preferably selected from the viewpoint of maintaining the breathability of the nonwoven fabric.
前記エンボスロールプレスは、金属エンボスロールと金属フラットロールの組合せの一対のロールに通して加工することが生産性の面から好ましい。不織ウェブの形態保持や最終的に得られる不織布の強度の観点から、エンボス面積率は５〜４０％、好ましくは５〜３０％、更に好ましくは６〜２０％である。エンボス形状は特に限定することはないが、円形状、楕円形状、ダイヤ形状、矩形状であることが好ましく、土木、建築、農業、産業、生活資材に好適に使用できる強伸度および柔軟性を有する不織布を得ることができる。 It is preferable from the viewpoint of productivity that the embossing roll press is processed through a pair of rolls of a combination of a metal embossing roll and a metal flat roll. From the viewpoint of maintaining the shape of the nonwoven web and the strength of the finally obtained nonwoven fabric, the embossed area ratio is 5 to 40%, preferably 5 to 30%, and more preferably 6 to 20%. The embossed shape is not particularly limited, but is preferably a circular shape, an elliptical shape, a diamond shape, or a rectangular shape, and has a high elongation and flexibility that can be suitably used for civil engineering, architecture, agriculture, industry, and daily life materials. The nonwoven fabric which has can be obtained.
本実施形態の不織布の引張強度は２０Ｎ／５０ｍｍ以上４００Ｎ／５０ｍｍ以下であり、且つ引張伸度は２０％以上７０％以下である。また、タフネス指数は以下の式（１）：
タフネス指数＝引張強度（Ｎ／５０ｍｍ）×引張伸度（％）／目付（ｇ／ｍ２） …式（１）
で算出され、好ましくは４０以上３００以下であり、より好ましくは４５以上２５０以下であり、更に好ましくは５０以上２００以下である。
引張強度、引張伸度、及びタフネス指標がこの範囲であると、不織布の加工性の面や土木、建築、農業、産業、生活資材として使用に適した範囲となる。タフネス指数が当範囲から外れると、工程上での布破断や、皺発生等の不具合が発生し易くなる。
The tensile strength of the nonwoven fabric of this embodiment is 20 N / 50 mm or more and 400 N / 50 mm or less, and tensile elongation is 20% or more and 70% or less. The toughness index is expressed by the following formula (1):
Toughness index = tensile strength (N / 50 mm) × tensile elongation (%) / weight per unit area (g / m 2 ) Formula (1)
And is preferably 40 or more and 300 or less, more preferably 45 or more and 250 or less, and still more preferably 50 or more and 200 or less.
When the tensile strength, tensile elongation, and toughness index are within this range, the nonwoven fabric is suitable for use as a workable surface, civil engineering, architecture, agriculture, industry, or daily life. When the toughness index is out of this range, problems such as cloth breakage and wrinkle generation on the process are likely to occur.
また、不織布を構成する繊維の繊度について制限はなく、通常のスパンボンド不織布に使用される繊維の繊度は生産性や通気性、風合いの点から、好ましくは０．７〜３．０ｄｔｅｘ程度、より好ましくは１．０〜２．８ｄｔｅｘ、更に好ましくは１．２〜２．５ｄｔｅｘである。 Moreover, there is no restriction | limiting about the fineness of the fiber which comprises a nonwoven fabric, The fineness of the fiber used for a normal spunbonded nonwoven fabric from the point of productivity, air permeability, and a texture, Preferably it is about 0.7-3.0 dtex, and more Preferably it is 1.0-2.8 dtex, More preferably, it is 1.2-2.5 dtex.
本実施形態の不織布の目付は、好ましくは８ｇ／ｍ２以上１００ｇ／ｍ２以下が好ましく、さらに好ましくは１０ｇ／ｍ２以上６０ｇ／ｍ２以下、特に好ましくは１０ｇ／ｍ２以上３０ｇ／ｍ２以下である。８ｇ／ｍ２以上であれば土木、建築、農業、産業、生活資材に使用される不織布としての強度を満足し、１００ｇ／ｍ２以下であれば、土木、建築、農業、産業、生活資材に使用される不織布の通気性を満足し、広範な用途への適応が可能である。 The basis weight of the nonwoven fabric of this embodiment is preferably 8 g / m 2 or more and 100 g / m 2 or less, more preferably 10 g / m 2 or more and 60 g / m 2 or less, and particularly preferably 10 g / m 2 or more and 30 g / m 2. It is as follows. If it is 8 g / m 2 or more, it satisfies the strength as a non-woven fabric used in civil engineering, construction, agriculture, industry, and living materials, and if it is 100 g / m 2 or less, it is suitable for civil engineering, building, agriculture, industry, and living materials. Satisfies the breathability of the nonwoven fabric used and can be applied to a wide range of applications.
本実施形態のスパンボンド不織布は、燃焼時二酸化炭素発生量を抑制することができ、使用後焼却廃棄している土木、建築、農業、産業、生活資材に好適に使用することができる。例えば、土木資材、建築資材であれば屋根下材、土木安定シート、断熱材面材、床材、ハウスラップなどが挙げられる。農業資材であれば、べた掛け、農資ポットなどが挙げられる。産業資材、生活資材であれば、食品包材、風呂敷、テープヤーン、靴資材、カイロ、ティーバック、クリーンカバー、メディカルガウン、自動車用資材、合紙、電線被覆材、テープ基材、膜機材、液体フィルター、エアーフィルター、不織布ワイパー、防護服などが挙げられる。尚、スパンボンド不織布が適応できるものであれば本用途は限定されるものではない。 The spunbond nonwoven fabric of the present embodiment can suppress the amount of carbon dioxide generated during combustion, and can be suitably used for civil engineering, construction, agriculture, industry, and daily life materials that are incinerated and discarded after use. For example, in the case of civil engineering materials and building materials, roofing materials, civil engineering stabilization sheets, heat insulating surface materials, flooring materials, house wraps and the like can be mentioned. In the case of agricultural materials, stickers, agricultural pots and the like can be mentioned. For industrial materials and household materials, food packaging materials, furoshiki, tape yarns, shoe materials, warmers, tea bags, clean covers, medical gowns, automotive materials, slip sheets, wire coating materials, tape base materials, membrane equipment, Examples include liquid filters, air filters, non-woven wipers and protective clothing. In addition, this application will not be limited if a spunbond nonwoven fabric can be applied.
本実施形態の不織布は二酸化炭素発生量抑制剤が繊維中に１５０〜２５０ｎｍの粒子径で均一分散している事が好ましい。さらに好ましくは１５０〜２００ｎｍであり、粒子径が１５０ｎｍ以上であれば二酸化炭素発生量を抑制する効果を発現し、２５０ｎｍ以下であれば凝集を引き起こすことがなく、紡糸工程において糸切れを発生することがない。繊維に均一分散している二酸化炭素発生量抑制剤の添加量は０．０３〜０．３０重量％が好ましい。好ましくは０．０５〜０．２５重量％、更に好ましくは０．１０〜０．２０重量％である。添加量が多すぎると、紡糸時糸切れを発生させる原因となるものである。特に繊維中における添加剤の凝集は繊維断面積が小さいため、紡糸時の繊維生産工程において曳糸性に顕著に影響する。他方、添加量が０．０３重量％未満では、二酸化炭素発生量抑制効果が発現しないものである。 In the nonwoven fabric of this embodiment, it is preferable that the carbon dioxide generation amount inhibitor is uniformly dispersed in the fiber with a particle diameter of 150 to 250 nm. More preferably, the particle diameter is 150 to 200 nm. If the particle diameter is 150 nm or more, an effect of suppressing the amount of carbon dioxide generated is expressed, and if it is 250 nm or less, aggregation is not caused and yarn breakage occurs in the spinning process. There is no. The addition amount of the carbon dioxide generation amount inhibitor uniformly dispersed in the fiber is preferably 0.03 to 0.30% by weight. Preferably it is 0.05-0.25 weight%, More preferably, it is 0.10-0.20 weight%. If the amount added is too large, thread breakage may occur during spinning. In particular, the aggregation of additives in the fiber has a small fiber cross-sectional area, and thus significantly affects the spinnability in the fiber production process during spinning. On the other hand, when the addition amount is less than 0.03% by weight, the carbon dioxide generation amount suppressing effect is not exhibited.
本願明細書中、二酸化炭素発生量抑制剤とは、二酸化炭素を化学的又は物理的に吸着する物質であればいかなるものでも構わないが、例えば、金属水酸化物、金属酸化物、アルミノケイ酸塩、チタン酸化合物、リチウムシリケート、シリカゲル、アルミナ、活性炭が挙げられる。 In the specification of the present application, the carbon dioxide generation amount inhibitor may be any substance as long as it is a substance that chemically or physically adsorbs carbon dioxide. For example, metal hydroxide, metal oxide, aluminosilicate is used. , Titanic acid compounds , lithium silicate, silica gel, alumina, activated carbon.
前記金属水酸化物としては、水酸化リチウム、水酸化ナトリウム、水酸化マグネシウム、水酸化カルシウム、水酸化バリウム等が挙げられる。 Examples of the metal hydroxide include lithium hydroxide, sodium hydroxide, magnesium hydroxide, calcium hydroxide, and barium hydroxide.
前記金属酸化物としては、酸化マグネシウム、酸化カルシウム、酸化亜鉛等が挙げられる。 Examples of the metal oxide include magnesium oxide, calcium oxide, and zinc oxide.
前記アルミノケイ酸塩としては、非晶質アルミノシリケート、天然ゼオライト、合成ゼオライト等が挙げられる。 Examples of the aluminosilicate include amorphous aluminosilicate, natural zeolite, and synthetic zeolite.
前記チタン酸化合物としては、チタン酸バリウム、オルソチタン酸バリウム等が挙げられる。 Examples of the titanate compound include barium titanate and barium orthotitanate.
前記ポリエステル系樹脂又はポリアミド系樹脂には分散助剤をされに添加してもよい。該における分散助剤は脂肪酸金属塩、高分子界面活性剤、両親媒性脂質のうち少なくとも１種であることができる。 A dispersion aid may be added to the polyester resin or polyamide resin. The dispersion aid may be at least one of a fatty acid metal salt, a polymeric surfactant, and an amphiphilic lipid.
例えば、微小なカプセル状のリポソームによって二酸化炭素発生量抑制剤及び結晶核剤を内包し、前記樹脂中に効率よく均一分散させることができる。 For example, a carbon dioxide generation amount inhibitor and a crystal nucleating agent can be encapsulated by minute capsule-like liposomes and efficiently dispersed uniformly in the resin.
また、二酸化炭素発生量抑制剤と分散助剤とを、分散処理、超臨界流体処理、超音波照射、撹拌処理等の方法で混合し、得られた二酸化炭素発生量抑制剤と分散助剤との混合物を、樹脂に添加することにより、樹脂との相溶性が低い二酸化炭素発生量抑制剤を凝集させずに、該樹脂に均一に分散させることができ、高い二酸化炭素の吸収効果を有する二酸化炭素発生量抑制樹脂を得ることができる。 Further, the carbon dioxide generation amount inhibitor and the dispersion aid are mixed by a method such as dispersion treatment, supercritical fluid treatment, ultrasonic irradiation, stirring treatment, etc. Is added to the resin, so that the carbon dioxide generation amount inhibitor having low compatibility with the resin can be uniformly dispersed in the resin without agglomeration, and has a high carbon dioxide absorption effect. A carbon generation suppression resin can be obtained.
二酸化炭素発生量抑制効果としては３０％以上が好ましく、より好ましくは４０％以上、さらに好ましくは５０％以上である。この範囲の二酸化炭素発生量抑制効果であれば、地球温暖化への影響から望まれている二酸化炭素削減効果と言える。 The carbon dioxide generation amount suppressing effect is preferably 30% or more, more preferably 40% or more, and further preferably 50% or more. If it is the carbon dioxide generation amount suppression effect of this range, it can be said that it is the carbon dioxide reduction effect desired from the influence on global warming.
本実施形態のスパンボンド不織布の製造においては、二酸化炭素発生量抑制剤が繊維中に均一に分散されているので、曳糸性が良く、紡糸工程において繊維の糸切れが発生しにくい。更に繊維の結晶配向性は低下しておらず、逆に紡糸条件を特定範囲で制御することで結晶配向性を向上させることができため、得られる繊維さらには形成される不織布の強伸度を向上させることができる。 In the production of the spunbonded nonwoven fabric of the present embodiment, the carbon dioxide generation amount inhibitor is uniformly dispersed in the fiber, so that the spinnability is good and fiber breakage hardly occurs in the spinning process. Furthermore, the crystal orientation of the fiber is not lowered, and conversely, the crystal orientation can be improved by controlling the spinning conditions within a specific range. Can be improved.
以下、実施例及び比較例により本発明を具体的に説明するが、本発明は下記実施例のみに限定されるものではない。
尚、実施例及び比較例において使用した各種特性の評価方法は下記のとおりであり、得られた物性を以下の表１及び２に示す。
EXAMPLES Hereinafter, although an Example and a comparative example demonstrate this invention concretely, this invention is not limited only to the following Example.
In addition, the evaluation method of the various characteristics used in the Example and the comparative example is as follows, and the obtained physical property is shown in the following Tables 1 and 2.
１．平均単糸繊度（ｄｔｅｘ）
不織布のＣＤ方向に５等分して１ｃｍ角の試験片を採取し、キーエンス社製マイクロスコープＶＨＸ−７００Ｆで繊維の直径を各２０点ずつ測定し、その平均値を算出した。
1. Average single yarn fineness (dtex)
A test piece of 1 cm square was sampled by dividing it into 5 parts in the CD direction of the nonwoven fabric, 20 diameters of each fiber were measured with a Keyence microscope VHX-700F, and the average value was calculated.
２．目付（ｇ／ｍ２）
ＪＩＳ−Ｌ１９０６に準じ、ＭＤ方向２０ｃｍ×ＣＤ方向５ｃｍの試験片を不織布のＣＤ方向に採取位置が均等になるように５枚採取して質量を測定し、その平均値を単位面積あたりの重量に換算して目付（ｇ／ｍ２）として求めた。
2. Weight per unit (g / m 2 )
In accordance with JIS-L1906, five test pieces of MD direction 20 cm × CD direction 5 cm were sampled so that the sampling positions were uniform in the CD direction of the nonwoven fabric, the mass was measured, and the average value was taken as the weight per unit area. The weight per unit area was calculated as a basis weight (g / m 2 ).
３．引張強度（Ｎ／５ｃｍ）、引張伸度（％）、タフネス指標
ＪＩＳ Ｌ−１９０６に準じ、ＣＤ方向均等になる様に、ＣＤ方向５ｃｍ、ＭＤ方向２０ｃｍの試験片を不織布のＣＤ方向に採取位置が均等になるように５枚採取して、引張試験機で、つかみ間隔１０ｃｍ、引張速度３０ｃｍ／分で測定した。ＭＤ方向各５点の試料を測定し、測定値を平均して引張強度と引張伸度を算出した。タフネス指数は以下の式：
タフネス指数＝引張強度（Ｎ／５ｃｍ）×引張伸度（％）／目付（ｇ／ｍ２）
から算出した。
3. Tensile strength (N / 5cm), tensile elongation (%), toughness index In accordance with JIS L-1906, the specimens in the CD direction 5cm and MD direction 20cm are collected in the CD direction of the nonwoven fabric so that they are uniform in the CD direction. Five samples were collected so as to be uniform, and measured with a tensile tester at a gripping interval of 10 cm and a tensile speed of 30 cm / min. Samples at five points in the MD direction were measured, and the measured values were averaged to calculate the tensile strength and the tensile elongation. The toughness index is:
Toughness index = tensile strength (N / 5 cm) × tensile elongation (%) / weight per unit (g / m 2 )
Calculated from
４．二酸化炭素発生量抑制剤の平均粒子径
粒度分布計（Particle Sizing System Co.製 NICOMP 380ZLS型）を用いて測定した。
4). The average particle size of the carbon dioxide generation inhibitor was measured using a particle size distribution analyzer (NICOMP 380ZLS type manufactured by Particle Sizing System Co.).
５．二酸化炭素発生量抑制剤の分散性
凝集する目安として剤粒子の大きさが４００ｎｍ以上とし、超高分解能電界放出形走査電子顕微鏡 S-5500（株式会社 日立ハイテクノロジーズ社製）明視野STEMにて20000倍率の繊維断面を観察した。４００ｎｍ以上のサイズの塊が無ければ分散性を「良」、あれば「悪」として評価した。
６．二酸化炭素発生量抑制効果
＜低温熱分解物の調製＞
一般的な自治体焼却炉で使用されているストーカ炉を想定し、各実施例で得られた二酸化炭素発生量抑制不織布と、二酸化炭素発生量抑制を含有しない不織布とをＴＧ／ＤＴＡ装置で雰囲気ガス窒素／空気、測定範囲３０〜４００℃、昇温速度１０℃／分、ガス流量２００ｍＬ／分条件で処理し低温熱分解物を得た。
＜不織布の二酸化炭素発生量抑制効果の測定＞
上記で調製した熱分解物１０ｍｇをＪＩＳ−Ｋ７２１７に準じ、空気下８００℃で１０分間燃焼させ、その際に発生した二酸化炭素を、熱伝導度検出器を備えたガスクロマトグラフで定量測定した。二酸化炭素発生量抑制剤を含有しない不織布から発生した二酸化炭素量と各実施例で得られた不織布から発生した二酸化炭素量との差の割合から二酸化炭素削減効果を算出した。
5. Dispersibility of carbon dioxide generation inhibitor As a measure of aggregation, the size of the agent particles should be 400 nm or more. Ultra-high resolution field emission scanning electron microscope S-5500 (manufactured by Hitachi High-Technologies Corporation) 20000 in bright field STEM A magnification fiber cross section was observed. The dispersibility was evaluated as “good” if there was no lump having a size of 400 nm or more, and “bad” if it was not.
6). Carbon dioxide generation suppression effect <Preparation of low-temperature pyrolysis product>
Assuming a stalker furnace used in general municipal incinerators, the carbon dioxide generation-suppressed nonwoven fabric obtained in each example and the nonwoven fabric that does not contain carbon dioxide generation-supplement suppression are added to the atmosphere gas using a TG / DTA device. A low temperature pyrolyzate was obtained by treatment under conditions of nitrogen / air, measurement range of 30 to 400 ° C., heating rate of 10 ° C./min, gas flow rate of 200 mL / min.
<Measurement of carbon dioxide generation suppression effect of nonwoven fabric>
In accordance with JIS-K7217, 10 mg of the pyrolyzate prepared above was combusted in air at 800 ° C. for 10 minutes, and carbon dioxide generated at that time was quantitatively measured with a gas chromatograph equipped with a thermal conductivity detector. The carbon dioxide reduction effect was calculated from the ratio of the difference between the amount of carbon dioxide generated from the nonwoven fabric containing no carbon dioxide generation inhibitor and the amount of carbon dioxide generated from the nonwoven fabric obtained in each example.
〔実施例１〕
ポリエチレンテレフタレート樹脂（融点２５４℃、密度１．３８ｇ／ｃｍ３）に平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０３重量％になる様に添加した。この二酸化炭素発生量抑制剤を添加したナイロン６樹脂をスパンボンド法により、単孔吐出量０．９０ｇ／ｍｉｎ・Ｈｏｌｅ、紡糸温度２９５℃で押出し、このフィラメント群をエアジェットによる高速気流牽引装置を使用して牽引し、移動捕集面に向けて押し出し、平均単糸繊度２．００ｄｔｅｘの不織布ウェブを得た。
[Example 1]
A carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was added to polyethylene terephthalate resin (melting point: 254 ° C., density: 1.38 g / cm 3 ) so that the pure content was 0.03% by weight. Nylon 6 resin added with carbon dioxide generation rate inhibitor is extruded by spunbond method at a single hole discharge rate of 0.90 g / min · Hole, spinning temperature of 295 ° C. Used tow and extruded toward the moving collection surface to obtain a nonwoven web having an average single yarn fineness of 2.00 dtex.
次いで、得られたウェブを、フラットロールとエンボスロール（パターン仕様：菱形、直行配列、縦横ピッチ２．０ｍｍ、圧着面積率１４．７％）の間に通して温度２４０℃と線圧３５ｋｇｆ／ｃｍで繊維同士を接着し、目付２０ｇ／ｍ２のスパンボンド不織布を得た。 Next, the obtained web was passed between a flat roll and an embossing roll (pattern specification: rhombus, orthogonal arrangement, vertical and horizontal pitch 2.0 mm, crimping area ratio 14.7%), temperature 240 ° C. and linear pressure 35 kgf / cm. The fibers were bonded together to obtain a spunbonded nonwoven fabric having a basis weight of 20 g / m 2 .
〔実施例２〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
[Example 2]
In the same manner as in Example 1, the average single yarn fineness was 2.45 dtex, and the basis weight was 20 g / m 2 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.09% by weight. Spunbond nonwoven fabric was obtained.
〔実施例３〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 3
An average single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was carried out in the same manner as in Example 1 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例４〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．３０重量％となる様に、実施例１と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 4
In the same manner as in Example 1, the average single yarn fineness was 2.45 dtex, and the basis weight was 20 g / m 2 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.30% by weight. Spunbond nonwoven fabric was obtained.
〔実施例５〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１と同様にして平均単糸繊度３．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 5
The average single yarn fineness is 3.00 dtex and the basis weight is 20 g / m 2 in the same manner as in Example 1 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm is 0.15% by weight. Spunbond nonwoven fabric was obtained.
〔実施例６〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１と同様にして平均単糸繊度１．４０ｄｔｅｘ、目付３０ｇ／ｍ２のスパンボンド不織布を得た。
Example 6
In the same manner as in Example 1, the average single yarn fineness was 1.40 dtex and the basis weight was 30 g / m 2 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例７〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１と同様にして平均単糸繊度０．０７ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 7
In the same manner as in Example 1, the average single yarn fineness was 0.07 dtex, and the basis weight was 20 g / m 2 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15% by weight. Spunbond nonwoven fabric was obtained.
〔実施例８〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付８ｇ／ｍ２のスパンボンド不織布を得た。
Example 8
In the same manner as in Example 1, the average single yarn fineness was 2.45 dtex, and the basis weight was 8 g / m 2 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15% by weight. Spunbond nonwoven fabric was obtained.
〔実施例９〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付６０ｇ／ｍ２のスパンボンド不織布を得た。
Example 9
In the same manner as in Example 1, the average single yarn fineness was 2.45 dtex, and the basis weight was 60 g / m 2 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15% by weight. Spunbond nonwoven fabric was obtained.
〔実施例１０〕
平均粒子径２００ｎｍの酸化マグネシウムからなる二酸化炭素発生量抑制剤を純分で０．１０重量％となる様に、実施例１と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 10
In the same manner as in Example 1, an average single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 is used so that the carbon dioxide generation amount inhibitor composed of magnesium oxide having an average particle diameter of 200 nm is 0.10 wt% in a pure content. A spunbond nonwoven fabric was obtained.
〔実施例１１〕
平均粒子径２００ｎｍのチタン酸バリウムからなる二酸化炭素発生量抑制剤を純分で０．１０重量％となる様に、実施例１と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 11
In the same manner as in Example 1, the average single yarn fineness of 2.00 dtex and the basis weight of 20 g / m 2 is set so that the carbon dioxide generation amount inhibitor composed of barium titanate having an average particle diameter of 200 nm is 0.10 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例１２〕
ポリブチレンテレフタレート樹脂（融点２２５℃、密度１．３８ｇ／ｃｍ３）に平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１０重量％となる様に添加し、実施例１と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 12
To a polybutylene terephthalate resin (melting point: 225 ° C., density: 1.38 g / cm 3 ), a carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle size of 200 nm is added to a pure content of 0.10% by weight, In the same manner as in Example 1, a spunbonded nonwoven fabric having an average single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was obtained.
〔実施例１３〕
平均粒子径が１５０ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 13
An average single yarn fineness of 2.45 dtex and a weight per unit area of 20 g / m were obtained in the same manner as in Example 1 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 150 nm was 0.09 wt% in a pure content. 2 spunbond nonwoven fabric was obtained.
〔実施例１４〕
平均粒子径が２５０ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 14
In the same manner as in Example 1, the average single yarn fineness was 2.45 dtex and the basis weight was 20 g / m so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle size of 250 nm was 0.09 wt% in a pure content. 2 spunbond nonwoven fabric was obtained.
〔実施例１５〕
ナイロン６樹脂（融点２２３℃、密度１．１４ｇ／ｃｍ３）に平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０３重量％になる様に添加した。この二酸化炭素発生量抑制剤を添加したナイロン６樹脂をスパンボンド法により、単孔吐出量０．９０ｇ／ｍｉｎ・Ｈｏｌｅ、紡糸温度２６５℃で押出し、このフィラメント群をエアジェットによる高速気流牽引装置を使用して牽引し、移動捕集面に向けて押し出し、平均単糸繊度２．００ｄｔｅｘの不織布ウェブを得た。
Example 15
A carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was added to nylon 6 resin (melting point: 223 ° C., density: 1.14 g / cm 3 ) so as to be 0.03% by weight. Nylon 6 resin added with carbon dioxide generation rate inhibitor is extruded by spunbonding at a single hole discharge rate of 0.90 g / min · Hole and a spinning temperature of 265 ° C. Used tow and extruded toward the moving collection surface to obtain a nonwoven web having an average single yarn fineness of 2.00 dtex.
次いで、得られたウェブを、フラットロールとエンボスロール（パターン仕様：直径０．４２５ｍｍ円形、千鳥配列、横ピッチ２．１ｍｍ、縦ピッチ１．１ｍｍ、圧着面積率６．３％）の間に通して温度１９０℃と線圧３５ｋｇｆ／ｃｍで繊維同士を接着し、目付２０ｇ／ｍ２のスパンボンド不織布を得た。 Next, the obtained web was passed between a flat roll and an embossing roll (pattern specification: circular with a diameter of 0.425 mm, staggered arrangement, horizontal pitch 2.1 mm, vertical pitch 1.1 mm, crimping area ratio 6.3%). The fibers were bonded at a temperature of 190 ° C. and a linear pressure of 35 kgf / cm to obtain a spunbonded nonwoven fabric having a basis weight of 20 g / m 2 .
〔実施例１６〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１３と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 16
An average single yarn fineness of 2.45 dtex and a basis weight of 20 g / m 2 was carried out in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.09 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例１７〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１３と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 17
An average single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was carried out in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例１８〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．３０重量％となる様に、実施例１３と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 18
An average single yarn fineness of 2.45 dtex and a basis weight of 20 g / m 2 was carried out in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.30% by weight. Spunbond nonwoven fabric was obtained.
〔実施例１９〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１３と同様にして平均単糸繊度３．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 19
The average single yarn fineness is 3.00 dtex, and the basis weight is 20 g / m 2 in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm is 0.15 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例２０〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１３と同様にして平均単糸繊度１．４０ｄｔｅｘ、目付３０ｇ／ｍ２のスパンボンド不織布を得た。
Example 20
An average single yarn fineness of 1.40 dtex and a basis weight of 30 g / m 2 were obtained in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例２１〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１３と同様にして平均単糸繊度０．０７ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 21
The average single yarn fineness was 0.07 dtex and the basis weight was 20 g / m 2 in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例２２〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１３と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付８ｇ／ｍ２のスパンボンド不織布を得た。
[Example 22]
An average single yarn fineness of 2.45 dtex and a basis weight of 8 g / m 2 were obtained in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例２３〕
平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１５重量％となる様に、実施例１３と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付６０ｇ／ｍ２のスパンボンド不織布を得た。
Example 23
An average single yarn fineness of 2.45 dtex and a basis weight of 60 g / m 2 was carried out in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 200 nm was 0.15 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例２４〕
平均粒子径２００ｎｍの酸化マグネシウムからなる二酸化炭素発生量抑制剤を純分で０．１０重量％となる様に、実施例１３と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 24
An average single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was applied in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of magnesium oxide having an average particle diameter of 200 nm was 0.10 wt% in a pure content. A spunbond nonwoven fabric was obtained.
〔実施例２５〕
平均粒子径２００ｎｍのチタン酸バリウムからなる二酸化炭素発生量抑制剤を純分で０．１０重量％となる様に、実施例１３と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 25
An average single yarn fineness of 2.00 dtex and a weight per unit area of 20 g / m 2 was obtained in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of barium titanate having an average particle diameter of 200 nm was 0.10 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例２６〕
ナイロン６６樹脂（融点２６５℃、密度１．１４ｇ／ｃｍ３）に平均粒子径２００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．１０重量％となる様に添加し、実施例１３と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 26
Nylon 66 resin (melting point: 265 ° C., density: 1.14 g / cm 3 ) was added with a carbon dioxide generation amount inhibitor consisting of sodium aluminosilicate having an average particle diameter of 200 nm so that the pure content would be 0.10 wt%. In the same manner as in Example 13, a spunbonded nonwoven fabric having an average single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was obtained.
〔実施例２７〕
平均粒子径１５０ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１３と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 27
An average single yarn fineness of 2.45 dtex and a weight per unit area of 20 g / m 2 was carried out in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 150 nm was 0.09 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔実施例２８〕
平均粒子径２５０ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１３と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。
Example 28
An average single yarn fineness of 2.45 dtex and a weight per unit area of 20 g / m 2 was obtained in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 250 nm was 0.09 wt% in a pure content. Spunbond nonwoven fabric was obtained.
〔比較例１〕
ポリエチレンテレフタレート樹脂（融点２５４℃、密度１．３８ｇ／ｃｍ３）にアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０２重量％となる様に、実施例１と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。比較例１の二酸化炭素発生量抑制剤添加量では、二酸化炭素発生量削減効果が２２％と低い値であった。
[Comparative Example 1]
In the same manner as in Example 1, a polyethylene terephthalate resin (melting point: 254 ° C., density: 1.38 g / cm 3 ) was averaged in the same manner as in Example 1 so that the carbon dioxide generation amount inhibitor consisting of sodium aluminosilicate was 0.02% by weight. A spunbonded nonwoven fabric having a single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was obtained. In the carbon dioxide generation amount inhibitor addition amount of Comparative Example 1, the carbon dioxide generation amount reduction effect was a low value of 22%.
〔比較例２〕
ポリエチレンテレフタレート樹脂（融点２５４℃、密度１．３８ｇ／ｃｍ３）を使用し実施例１と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。比較例２では二酸化炭素発生量抑制剤を添加していないため、抑制効果が発現しなかった。
[Comparative Example 2]
Using a polyethylene terephthalate resin (melting point 254 ° C., density 1.38 g / cm 3 ), a spunbonded nonwoven fabric having an average single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was obtained in the same manner as in Example 1. In Comparative Example 2, since the carbon dioxide generation amount inhibitor was not added, the suppression effect was not exhibited.
〔比較例３〕
ポリエチレンテレフタレート樹脂（融点２５４℃、密度１．３８ｇ／ｃｍ３）にアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．３５重量％となる様に、実施例１と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得たが、紡糸時の糸切れが多く、品位の悪い不織布となった。
[Comparative Example 3]
In the same manner as in Example 1, an average amount of a carbon dioxide generation inhibitor composed of sodium aluminosilicate was added to a polyethylene terephthalate resin (melting point: 254 ° C., density: 1.38 g / cm 3 ) in the same manner as in Example 1. A spunbonded nonwoven fabric having a single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was obtained, but there were many yarn breaks during spinning, and the nonwoven fabric was poor in quality.
〔比較例４〕
平均粒子径１００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。比較例４では二酸化炭素発生量抑制剤の平均粒子径が１５０ｎｍ未満であったため、二酸化炭素発生量削減効果が２５％と低い値となった。
[Comparative Example 4]
In the same manner as in Example 1, the average single yarn fineness was 2.45 dtex, and the weight per unit area was 20 g / m 2 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 100 nm was 0.09% by weight. Spunbond nonwoven fabric was obtained. In Comparative Example 4, since the average particle diameter of the carbon dioxide generation amount inhibitor was less than 150 nm, the carbon dioxide generation amount reduction effect was a low value of 25%.
〔比較例５〕
平均粒子径４００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た 。比較例５では二酸化炭素発生量抑制剤の平均粒子径２５０ｎｍを超えていたため、紡糸時の糸切れが多く、品位の悪い不織布となった。
[Comparative Example 5]
In the same manner as in Example 1, the average single yarn fineness was 2.45 dtex, and the basis weight was 20 g / m 2 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 400 nm was 0.09% by weight. Spunbond nonwoven fabric was obtained. In Comparative Example 5, since the average particle diameter of the carbon dioxide generation amount inhibitor exceeded 250 nm, there was a lot of yarn breakage during spinning, and the nonwoven fabric was poor in quality.
〔比較例６〕
ナイロン６樹脂（融点２２３℃、密度１．１４ｇ／ｃｍ３）にアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０２重量％となる様に、実施例１３と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。比較例１の二酸化炭素発生量抑制剤添加量では、二酸化炭素発生量削減効果が２５％と低い値であった。
[Comparative Example 6]
In the same manner as in Example 13, the nylon 6 resin (melting point: 223 ° C., density: 1.14 g / cm 3 ) and the carbon dioxide generation amount inhibitor consisting of sodium aluminosilicate were 0.02% by weight in pure content. A spunbonded nonwoven fabric having a single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was obtained. In the carbon dioxide generation amount inhibitor addition amount of Comparative Example 1, the carbon dioxide generation amount reduction effect was a low value of 25%.
〔比較例７〕
ナイロン６樹脂（融点２２３℃、密度１．１４ｇ／ｃｍ３）を使用し実施例１３と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。比較例２では二酸化炭素発生量抑制剤を添加していないため、抑制効果が発現しなかった。
[Comparative Example 7]
Using a nylon 6 resin (melting point 223 ° C., density 1.14 g / cm 3 ), a spunbonded nonwoven fabric having an average single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was obtained in the same manner as in Example 13. In Comparative Example 2, since the carbon dioxide generation amount inhibitor was not added, the suppression effect was not exhibited.
〔比較例８〕
ナイロン６樹脂（融点２２３℃、密度１．１４ｇ／ｃｍ３）にアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．３５重量％となる様に、実施例１３と同様にして平均単糸繊度２．００ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得たが、紡糸時の糸切れが多く、品位の悪い不織布となった。
[Comparative Example 8]
In the same manner as in Example 13, an average amount of carbon dioxide generation inhibitor composed of sodium aluminosilicate was added to nylon 6 resin (melting point: 223 ° C., density: 1.14 g / cm 3 ) in the same manner as in Example 13. A spunbonded nonwoven fabric having a single yarn fineness of 2.00 dtex and a basis weight of 20 g / m 2 was obtained, but there were many yarn breaks during spinning, and the nonwoven fabric was poor in quality.
〔比較例９〕
平均粒子径１００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１３と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。比較例９では二酸化炭素発生量抑制剤の平均粒子径が１５０ｎｍ未満であったため、二酸化炭素発生量削減効果が２５％と低い値であった。
[Comparative Example 9]
An average single yarn fineness of 2.45 dtex and a weight per unit area of 20 g / m 2 was carried out in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 100 nm was 0.09% by weight in a pure content. Spunbond nonwoven fabric was obtained. In Comparative Example 9, since the average particle size of the carbon dioxide generation amount inhibitor was less than 150 nm, the carbon dioxide generation amount reduction effect was a low value of 25%.
〔比較例１０〕
平均粒子径４００ｎｍのアルミノケイ酸ナトリウムからなる二酸化炭素発生量抑制剤を純分で０．０９重量％となる様に、実施例１３と同様にして平均単糸繊度２．４５ｄｔｅｘ、目付２０ｇ／ｍ２のスパンボンド不織布を得た。比較例１０では二酸化炭素発生量抑制剤の平均粒子径２５０ｎｍを超えていたため、紡糸時の糸切れが多く、品位の悪い不織布となった。
[Comparative Example 10]
An average single yarn fineness of 2.45 dtex and a weight per unit area of 20 g / m 2 was carried out in the same manner as in Example 13 so that the carbon dioxide generation amount inhibitor composed of sodium aluminosilicate having an average particle diameter of 400 nm was 0.09% by weight. Spunbond nonwoven fabric was obtained. In Comparative Example 10, since the average particle diameter of the carbon dioxide generation amount inhibitor exceeded 250 nm, there were many yarn breaks during spinning, and the nonwoven fabric was poor in quality.
本発明のスパンボンド不織布は、燃焼時二酸化炭素発生量を抑制することができ、且つ、強伸度を有し、生産上の工程安定性や着用時の破断を抑制する効果を奏するため、土木、建築、農業、産業、生活資材用途に好適に利用可能である。 The spunbonded nonwoven fabric of the present invention can suppress the amount of carbon dioxide generated during combustion, has high elongation, and exhibits the effects of suppressing process stability during production and breaking during wearing. It can be suitably used for construction, agriculture, industry and daily life materials.
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