JP4249592B2 - Combustible non-woven fabric and method for producing the same - Google Patents
Combustible non-woven fabric and method for producing the same Download PDFInfo
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- JP4249592B2 JP4249592B2 JP2003366296A JP2003366296A JP4249592B2 JP 4249592 B2 JP4249592 B2 JP 4249592B2 JP 2003366296 A JP2003366296 A JP 2003366296A JP 2003366296 A JP2003366296 A JP 2003366296A JP 4249592 B2 JP4249592 B2 JP 4249592B2
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- JP
- Japan
- Prior art keywords
- nonwoven fabric
- metal oxide
- oxide particles
- combustion
- antioxidant
- 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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- 239000004745 nonwoven fabric Substances 0.000 title claims description 93
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000002245 particle Substances 0.000 claims description 67
- 229910044991 metal oxide Inorganic materials 0.000 claims description 59
- 150000004706 metal oxides Chemical class 0.000 claims description 53
- 238000002485 combustion reaction Methods 0.000 claims description 36
- 239000000835 fiber Substances 0.000 claims description 33
- 239000003963 antioxidant agent Substances 0.000 claims description 24
- 230000003078 antioxidant effect Effects 0.000 claims description 22
- -1 polyethylene Polymers 0.000 claims description 12
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 11
- 229910052698 phosphorus Inorganic materials 0.000 claims description 11
- 239000011574 phosphorus Substances 0.000 claims description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 10
- 229920000098 polyolefin Polymers 0.000 claims description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- 238000002074 melt spinning Methods 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- 230000003197 catalytic effect Effects 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 4
- 229920005672 polyolefin resin Polymers 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 4
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 239000002131 composite material Substances 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 36
- 238000009987 spinning Methods 0.000 description 26
- 238000000034 method Methods 0.000 description 22
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 20
- 229920000642 polymer Polymers 0.000 description 17
- 230000007423 decrease Effects 0.000 description 14
- 150000002013 dioxins Chemical class 0.000 description 13
- 230000006870 function Effects 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 11
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 11
- 229910002092 carbon dioxide Inorganic materials 0.000 description 10
- 239000001569 carbon dioxide Substances 0.000 description 10
- 239000004594 Masterbatch (MB) Substances 0.000 description 8
- 239000000567 combustion gas Substances 0.000 description 8
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 8
- 238000005453 pelletization Methods 0.000 description 8
- 239000002530 phenolic antioxidant Substances 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- 238000005979 thermal decomposition reaction Methods 0.000 description 7
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- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
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- 238000002411 thermogravimetry Methods 0.000 description 6
- 239000002699 waste material Substances 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000005304 joining Methods 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 230000002745 absorbent Effects 0.000 description 3
- 239000002250 absorbent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 238000004056 waste incineration Methods 0.000 description 3
- ROHFBIREHKPELA-UHFFFAOYSA-N 2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]prop-2-enoic acid;methane Chemical compound C.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O.CC(C)(C)C1=CC(CC(=C)C(O)=O)=CC(C(C)(C)C)=C1O ROHFBIREHKPELA-UHFFFAOYSA-N 0.000 description 2
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 239000010849 combustible waste Substances 0.000 description 2
- 230000002354 daily effect Effects 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 229910052738 indium Inorganic materials 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 2
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229910006540 α-FeOOH Inorganic materials 0.000 description 2
- FEODVXCWZVOEIR-UHFFFAOYSA-N (2,4-ditert-butylphenyl) octyl hydrogen phosphite Chemical compound CCCCCCCCOP(O)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C FEODVXCWZVOEIR-UHFFFAOYSA-N 0.000 description 1
- JWCYRADIWYQGTO-UHFFFAOYSA-N 1,1-bis(2,4-ditert-butylphenyl)-2,2-bis(hydroxymethyl)propane-1,3-diol phosphorous acid Chemical compound P(O)(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C JWCYRADIWYQGTO-UHFFFAOYSA-N 0.000 description 1
- KBZQKRFMZFQXHE-UHFFFAOYSA-N 1,1-bis(2,6-ditert-butyl-4-methylphenyl)-2,2-bis(hydroxymethyl)propane-1,3-diol phosphorous acid Chemical compound P(O)(O)O.C(C)(C)(C)C1=C(C(=CC(=C1)C)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1C(C)(C)C)C)C(C)(C)C KBZQKRFMZFQXHE-UHFFFAOYSA-N 0.000 description 1
- GJDRKHHGPHLVNI-UHFFFAOYSA-N 2,6-ditert-butyl-4-(diethoxyphosphorylmethyl)phenol Chemical compound CCOP(=O)(OCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 GJDRKHHGPHLVNI-UHFFFAOYSA-N 0.000 description 1
- QSRJVOOOWGXUDY-UHFFFAOYSA-N 2-[2-[2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]ethoxy]ethoxy]ethyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCCOCCOCCOC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 QSRJVOOOWGXUDY-UHFFFAOYSA-N 0.000 description 1
- PFANXOISJYKQRP-UHFFFAOYSA-N 2-tert-butyl-4-[1-(5-tert-butyl-4-hydroxy-2-methylphenyl)butyl]-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(CCC)C1=CC(C(C)(C)C)=C(O)C=C1C PFANXOISJYKQRP-UHFFFAOYSA-N 0.000 description 1
- BKZXZGWHTRCFPX-UHFFFAOYSA-N 2-tert-butyl-6-methylphenol Chemical compound CC1=CC=CC(C(C)(C)C)=C1O BKZXZGWHTRCFPX-UHFFFAOYSA-N 0.000 description 1
- PZRWFKGUFWPFID-UHFFFAOYSA-N 3,9-dioctadecoxy-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Chemical compound C1OP(OCCCCCCCCCCCCCCCCCC)OCC21COP(OCCCCCCCCCCCCCCCCCC)OC2 PZRWFKGUFWPFID-UHFFFAOYSA-N 0.000 description 1
- MDWVSAYEQPLWMX-UHFFFAOYSA-N 4,4'-Methylenebis(2,6-di-tert-butylphenol) Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MDWVSAYEQPLWMX-UHFFFAOYSA-N 0.000 description 1
- QRLSTWVLSWCGBT-UHFFFAOYSA-N 4-((4,6-bis(octylthio)-1,3,5-triazin-2-yl)amino)-2,6-di-tert-butylphenol Chemical compound CCCCCCCCSC1=NC(SCCCCCCCC)=NC(NC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=N1 QRLSTWVLSWCGBT-UHFFFAOYSA-N 0.000 description 1
- PRWJPWSKLXYEPD-UHFFFAOYSA-N 4-[4,4-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butan-2-yl]-2-tert-butyl-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(C)CC(C=1C(=CC(O)=C(C=1)C(C)(C)C)C)C1=CC(C(C)(C)C)=C(O)C=C1C PRWJPWSKLXYEPD-UHFFFAOYSA-N 0.000 description 1
- ZVVFVKJZNVSANF-UHFFFAOYSA-N 6-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]hexyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCCCCCCOC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 ZVVFVKJZNVSANF-UHFFFAOYSA-N 0.000 description 1
- UYQYTUYNNYZATF-UHFFFAOYSA-N 6-methyl-4,6-bis(octylsulfanylmethyl)cyclohexa-1,3-dien-1-ol Chemical compound CCCCCCCCSCC1=CC=C(O)C(C)(CSCCCCCCCC)C1 UYQYTUYNNYZATF-UHFFFAOYSA-N 0.000 description 1
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- CGRTZESQZZGAAU-UHFFFAOYSA-N [2-[3-[1-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]-2-methylpropan-2-yl]-2,4,8,10-tetraoxaspiro[5.5]undecan-9-yl]-2-methylpropyl] 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCC(C)(C)C2OCC3(CO2)COC(OC3)C(C)(C)COC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 CGRTZESQZZGAAU-UHFFFAOYSA-N 0.000 description 1
- VSVVZZQIUJXYQA-UHFFFAOYSA-N [3-(3-dodecylsulfanylpropanoyloxy)-2,2-bis(3-dodecylsulfanylpropanoyloxymethyl)propyl] 3-dodecylsulfanylpropanoate Chemical compound CCCCCCCCCCCCSCCC(=O)OCC(COC(=O)CCSCCCCCCCCCCCC)(COC(=O)CCSCCCCCCCCCCCC)COC(=O)CCSCCCCCCCCCCCC VSVVZZQIUJXYQA-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229910001566 austenite Inorganic materials 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910001593 boehmite Inorganic materials 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910001648 diaspore Inorganic materials 0.000 description 1
- 238000004649 discoloration prevention Methods 0.000 description 1
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 238000010035 extrusion spinning Methods 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229910001679 gibbsite Inorganic materials 0.000 description 1
- 229910052598 goethite Inorganic materials 0.000 description 1
- 239000011019 hematite Substances 0.000 description 1
- 229910052595 hematite Inorganic materials 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 1
- AEIXRCIKZIZYPM-UHFFFAOYSA-M hydroxy(oxo)iron Chemical compound [O][Fe]O AEIXRCIKZIZYPM-UHFFFAOYSA-M 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
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- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
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- 150000004692 metal hydroxides Chemical class 0.000 description 1
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
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- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
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- 230000001629 suppression Effects 0.000 description 1
- LVEOKSIILWWVEO-UHFFFAOYSA-N tetradecyl 3-(3-oxo-3-tetradecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCC LVEOKSIILWWVEO-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
- 229910006299 γ-FeOOH Inorganic materials 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Nonwoven Fabrics (AREA)
Description
本発明は、紡糸性が良好で、焼却時の燃焼性に優れた易燃焼性不織布、特に完全燃焼性に優れ、混在する可燃物の燃焼効率を促進させ、ダイオキシン類等の有害成分の発生を抑制することができる、環境に優しい易燃焼性不織布およびその製造方法に関する。 The present invention is an easily combustible non-woven fabric having good spinnability and excellent combustibility during incineration, particularly excellent complete combustibility, promoting combustion efficiency of mixed combustible materials, and generating harmful components such as dioxins. The present invention relates to an environment-friendly easily combustible nonwoven fabric that can be suppressed and a method for producing the same.
近年、生活水準の向上により種々の新しい商品が出現し、産業廃棄物や一般家庭から排出されるごみの量が増加している。これらのうち不燃性ごみは埋立処理されているが、可燃性ごみは一般的には焼却処理されている。しかし、ごみの燃焼時に発生する有害物質、特にダイオキシン類の発生は、焼却設備の制約等に関連する重要な問題となっている。このダイオキシンは燃焼過程での不完全燃焼によってその前駆体となるベンゼンと塩素化合物が反応して生成すると考えられている。このダイオキシン類の抑制には、ダイオキシン類が生成しないように燃焼条件を制御する方法、ダイオキシン類の生成後にこれを分解または除去する方法が知られているが、その発生を未然に防止することが基本的な対策となる。そのためには、ダイオキシン類の出発物質であるベンゼンや塩素化合物の発生を低減させるべく、ごみの完全燃焼化を図ることが必要となる。 In recent years, various new products have appeared due to the improvement of living standards, and the amount of industrial waste and garbage discharged from ordinary households has increased. Of these, incombustible waste is landfilled, but combustible waste is generally incinerated. However, the generation of harmful substances, especially dioxins, generated during the combustion of garbage is an important problem related to restrictions on incineration facilities. This dioxin is thought to be produced by the reaction of benzene and chlorine compounds, which are precursors, due to incomplete combustion during the combustion process. In order to suppress dioxins, there are known a method for controlling combustion conditions so that dioxins are not generated, and a method for decomposing or removing dioxins after they are generated. This is a basic measure. For this purpose, it is necessary to completely burn the waste in order to reduce the generation of benzene and chlorine compounds, which are starting materials for dioxins.
具体的には、ごみ焼却時のダイオキシン類発生の抑制方法として、焼却炉の燃焼室に燃焼促進機能を有する粒子状の酸化金属触媒を直接吹き込む方法が提案されている。しかし、この方法ではごみの形態によりその内部にまで酸化金属触媒を分散させることができないことがあり、効率が悪いという問題があった。またプラスチックフィルム製のごみ袋や買物袋に酸化金属触媒を含有させることにより、焼却時に可燃ごみの焼却効率を向上させる方法が提案されている(例えば、特許文献1、2、3参照)。しかし、この方法は単に樹脂成分に酸化金属触媒を添加してフィルム化するものであり、この方法をそのまま不織布に採用すると繊維の紡糸中に糸切れが多発し、繊維化できず、不織布を製造することができないという問題があった。
近年、不織布は、通気性や布帛的な機能を有することから、オムツやナプキンなどの衛生材料を始め、ウェットティッシュや生ごみの水切り袋などの生活資材、また医療用の簡易マスクやメディカルガウンなどの種々の分野において、使い捨て素材としてその使用量が著しく増大しており、これらは毎日のようにごみとして廃棄されている。従って、ごみ焼却時の不完全燃焼の抑制するために、不織布自体に燃焼促進機能を付与してごみ焼却時の効率的な燃焼を行うことが求められている。また不織布を構成する繊維を細くすることは燃焼効率の点から有利となる。しかし、燃焼促進機能を有する酸化金属触媒を単にポリマーに添加して紡糸すると上記したように紡糸中に糸切れが多発し、特に高速紡糸領域では繊維を細く紡糸することは困難であった。
Specifically, a method of directly blowing a particulate metal oxide catalyst having a combustion promoting function into a combustion chamber of an incinerator has been proposed as a method for suppressing the generation of dioxins during waste incineration. However, this method has a problem in that the metal oxide catalyst cannot be dispersed in the interior depending on the form of the dust, and the efficiency is poor. In addition, a method for improving the incineration efficiency of combustible waste at the time of incineration by including a metal oxide catalyst in a plastic film waste bag or a shopping bag has been proposed (see, for example, Patent Documents 1, 2, and 3). However, this method simply adds a metal oxide catalyst to the resin component to form a film. If this method is applied to a nonwoven fabric as it is, yarn breaks occur frequently during fiber spinning, and the fiber cannot be made, producing a nonwoven fabric. There was a problem that could not be done.
In recent years, non-woven fabrics have breathable and fabric-like functions, so hygiene materials such as diapers and napkins, daily life materials such as wet tissue and garbage draining bags, simple medical masks and medical gowns, etc. In various fields, the amount of use as a disposable material has increased remarkably, and these are discarded as garbage every day. Therefore, in order to suppress incomplete combustion at the time of waste incineration, it is required to impart a combustion promoting function to the nonwoven fabric itself to perform efficient combustion at the time of waste incineration. Further, it is advantageous from the viewpoint of combustion efficiency to make the fibers constituting the nonwoven fabric thinner. However, when a metal oxide catalyst having a combustion accelerating function is simply added to a polymer and spun, yarn breakage frequently occurs during spinning as described above, and it has been difficult to spin fibers finely, particularly in the high-speed spinning region.
また、液不透過性の裏面層と液保持性の吸収層を備えた吸収性物品のいずれかの部位に鉄系燃焼促進剤を含有させて使用済吸収性物品の焼却時の水分等の存在による燃焼温度の低下を防止する方法が提案されている(例えば、特許文献4等)。しかし、この場合も鉄系燃焼促進剤を樹脂に含有させてフィルム状とするものであり、燃焼促進剤を添加した樹脂を紡糸して不織布とする場合の問題およびこれを解決するための方法は提案されていない。
本発明の課題は、上記技術の問題点を解決し、細い繊維を安定的に紡糸して布帛的機能を維持し、かつ焼却時の有害成分の発生を抑制し、しかも優れた燃焼性を備えた易燃焼性不織布およびその製造方法を提供することにある。 The object of the present invention is to solve the above-mentioned problems of the technology, stably spin fine fibers to maintain the fabric function, suppress the generation of harmful components during incineration, and have excellent combustibility. Another object of the present invention is to provide an easily combustible nonwoven fabric and a method for producing the same.
本発明者らは、上記課題について鋭意検討した結果、燃焼促進機能を有する金属酸化物類粒子をポリマーに含有させて紡糸する際に発生する糸切れの要因が、金属酸化物類粒子の粒子径や混練性、さらにはマスターバッチとしてペレット状にする際およびマスターバッチを添加してポリマーを押出紡糸する際に発生する熱分解や酸化だけでなく、金属酸化物類粒子の存在によりポリマーが酸化されるためであることを突き止め、この酸化を防ぐために特定の酸化防止剤を併用することにより、紡糸の安定化が可能になることを見い出し、本発明を完成するに至った。
すなわち、本願で特許請求される発明は以下の通りである。
As a result of intensive studies on the above problems, the present inventors have found that the cause of yarn breakage that occurs when spinning by adding metal oxide particles having a combustion promoting function to the polymer is the particle size of the metal oxide particles. In addition to the thermal decomposition and oxidation that occur when pelletizing as a masterbatch and when the masterbatch is added to extrude the polymer, the polymer is oxidized by the presence of metal oxide particles. In order to prevent this oxidation, the inventors have found that spinning can be stabilized by using a specific antioxidant in combination, and the present invention has been completed.
That is, the invention claimed in the present application is as follows.
(1)3.3dtex以下の繊度を有するポリオレフィン系繊維を含む不織布であって、該ポリオレフィン系繊維が、燃焼に対する活性触媒機能を有する金属酸化物類粒子と、フェノール系、リン系および硫黄系から選ばれた少なくとも1種の酸化防止剤とを含有し、該金属酸化物類粒子の粒子径が1.5μm以下、およびその含有量が、0.05〜5重量%であり、かつ該酸化防止剤の含有量が0.1〜0.5重量%であることを特徴とする易燃焼性不織布。
(2)前記金属酸化物類粒子が、アルミニウム系金属酸化物類および/または鉄系金属酸化物類であることを特徴とする(1)に記載の易燃焼性不織布。
(3)前記ポリオレフィン系繊維が、ポリエチレン、ポリプロピレン、エチレン・プロピレン共重合物およびオクテン・プロピレン共重合物の少なくとも1種を含む繊維またはこれらの複合繊維であることを特徴とする(1)または(2)に記載の易燃焼性不織布。
(4)3.3dtex以下の繊度を有するポリオレフィン系樹脂成分を溶融紡糸して不織布を製造するに際し、該ポリオレフィン系樹脂成分に、燃焼に対する活性触媒機能を有する、粒子径が1.5μm以下の金属酸化物類粒子を0.05〜5重量%、およびフェノール系、リン系および硫黄系から選ばれた少なくとも1種の酸化防止剤を0.1〜0.5重量%含有させて溶融紡糸し、不織布に形成することを特徴とする(1)に記載の易燃焼性不織布の製造方法。
(1) A non-woven fabric containing polyolefin fibers having a fineness of 3.3 dtex or less , wherein the polyolefin fibers are composed of metal oxide particles having an active catalytic function for combustion, phenolic, phosphorous and sulfur At least one selected antioxidant, the particle size of the metal oxide particles is 1.5 μm or less, and the content thereof is 0.05 to 5% by weight, and the antioxidant An easily combustible nonwoven fabric characterized in that the content of the agent is 0.1 to 0.5% by weight .
( 2 ) The readily combustible nonwoven fabric according to ( 1 ), wherein the metal oxide particles are aluminum metal oxides and / or iron metal oxides.
( 3 ) The polyolefin fiber is a fiber containing at least one of polyethylene, polypropylene, an ethylene / propylene copolymer and an octene / propylene copolymer, or a composite fiber thereof ( 1) or ( 2 ) The nonflammable nonwoven fabric described in 2 ).
( 4 ) When producing a nonwoven fabric by melt spinning a polyolefin resin component having a fineness of 3.3 dtex or less, the polyolefin resin component has an active catalytic function against combustion , and a metal having a particle diameter of 1.5 μm or less. Melt spinning containing 0.05 to 5% by weight of oxide particles and 0.1 to 0.5% by weight of at least one antioxidant selected from phenol, phosphorus and sulfur , It forms in a nonwoven fabric, The manufacturing method of the easily combustible nonwoven fabric as described in ( 1) characterized by the above-mentioned .
本発明によれば、不織布を構成するポリオレフィン系繊維に特定の酸化防止剤および金属酸化物類を含有しているため、紡糸時の糸切れがなく、不織布の製造が容易であり、また繊維を細く紡糸することができ、優れた通気性と柔軟性を備えた布帛的機能を有する易燃焼性の不織布を得ることができる。さらにこの不織布はごみとして焼却した際の燃焼特性に優れているため、ダイオキシン等の有害成分の発生を抑制することができる。従って、本発明の易燃焼性不織布は、オムツやナプキンなどの衛生材料、ウェットティッシュや生ごみの水切り袋、包材などの生活資材、また医療用では簡易マスクやメディカルガウンなどの使い捨て素材に特に好適に使用することができる。 According to the present invention, since the polyolefin-based fiber constituting the nonwoven fabric contains a specific antioxidant and metal oxides, there is no yarn breakage during spinning, and the nonwoven fabric can be easily produced. It is possible to obtain a flammable nonwoven fabric that can be spun finely and has a fabric function with excellent breathability and flexibility. Furthermore, since this nonwoven fabric has excellent combustion characteristics when incinerated as waste, generation of harmful components such as dioxins can be suppressed. Therefore, the non-flammable nonwoven fabric of the present invention is particularly suitable for sanitary materials such as diapers and napkins, living materials such as wet tissues and garbage draining bags, packaging materials, and disposable materials such as simple masks and medical gowns for medical use. It can be preferably used.
以下、本発明について説明する。
本発明の易燃焼性不織布は、不織布を構成するポリオレフィン系繊維に、燃焼に対する活性触媒機能を有する金属酸化物類粒子と、フェノール系、リン系および硫黄系から選ばれた少なくも1種の酸化防止剤を含有させることにより得られる。該酸化防止剤の含有量は上記金属酸化物類粒子によるポリオレフィン系繊維の製造中の酸化劣化を防止するに充分な程度の量とされるが、好ましくは0.05〜1重量%である。
本発明に用いられるポリオレフィン系繊維の素材としては、疎水性、強度、可撓性などの点から、ポリエチレン、ポリプロピレン、エチレン・プロピレン共重合物、オクテン・プロピレン共重合物などが好ましく、これらは単独でまたは2種以上混合して用いることができ、またこれらを複合して用いてもよい。繊維の繊度は10dtex以下とするのが好ましく、特に衛材用、生活資材、医療用などの布帛としての柔軟性、ソフトな触感が要求される場合には3.3dtex以下とするのが好ましい。
The present invention will be described below.
The easily combustible nonwoven fabric of the present invention comprises at least one kind of oxide selected from the group consisting of metal oxide particles having an active catalytic function for combustion, and phenolic, phosphorus and sulfur based on polyolefin fibers constituting the nonwoven fabric. It is obtained by containing an inhibitor. The content of the antioxidant is set to an amount sufficient to prevent oxidative degradation during the production of the polyolefin fiber by the metal oxide particles, but is preferably 0.05 to 1% by weight.
The polyolefin fiber material used in the present invention is preferably polyethylene, polypropylene, ethylene / propylene copolymer, octene / propylene copolymer, etc., from the viewpoint of hydrophobicity, strength, flexibility, and the like. Or a mixture of two or more of these may be used in combination. The fineness of the fiber is preferably 10 dtex or less, particularly 3.3 dtex or less when flexibility and soft tactile sensation are required as fabrics for sanitary materials, daily life materials, and medical use.
不織布を構成する繊維の形態には特に限定はなく、いわゆるカーディング、抄紙法等による短繊維でも、または長繊維でもよいが、強力、生産性の点からは連続フィラメントを用いるのが好ましい。この不織布は、例えば、スパンボンド法により溶融紡糸された連続フィラメントをウェブとし、これを接合して不織布とするのが好ましい。ウェブの接合には、接着剤を用いて接合する方法、低融点繊維や複合繊維により接合する方法、ホットメルトバインダーをウェブ形成中に散布して溶融接合する方法、ニードルパンチ、水流等で繊維を交絡することによりえることができる。不織布の強度および柔軟性を高めるために部分熱圧着により接合するのが好ましい。部分熱圧着する際の熱圧着面積率は、強度保持と柔軟性の点から、5〜50%が好ましい。部分熱圧着は、例えば超音波法により、または加熱したエンボスロールとフラットロールの間にウェブを通して行うことができ、これにより、例えば、ピンポイント状、矩形状等の接合点であるエンボス模様が全面に散点する不織布が得られる。 The form of the fibers constituting the nonwoven fabric is not particularly limited, and may be short fibers or long fibers by so-called carding, paper making method or the like, but continuous filaments are preferably used from the viewpoint of strength and productivity. The nonwoven fabric is preferably made of a continuous filament melt-spun by a spunbond method, for example, and joined to form a nonwoven fabric. For joining the web, a method of joining using an adhesive, a method of joining with a low-melting fiber or a composite fiber, a method of spraying a hot melt binder during web formation, a melt joining method, a needle punch, a water stream, etc. It can be obtained by confounding. In order to increase the strength and flexibility of the nonwoven fabric, it is preferable to join by partial thermocompression bonding. The area ratio of thermocompression bonding during partial thermocompression bonding is preferably 5 to 50% from the viewpoint of strength retention and flexibility. The partial thermocompression bonding can be performed, for example, by an ultrasonic method or through a web between a heated embossing roll and a flat roll, so that, for example, an embossed pattern that is a joint point such as a pinpoint shape or a rectangular shape is formed on the entire surface. A non-woven fabric that is scattered is obtained.
本発明に用いられる金属酸化物類粒子は、燃焼に対する活性触媒機能、すなわち燃焼時に活性酸素を発生して燃焼を促進させる作用を有するものであり、金属酸化物のほか、加熱により酸化物を形成する金属水酸化物等を含む。該金属酸化物類粒子としては、例えば、アルミニウム系金属酸化物類、鉄系金属酸化物類などが挙げられる。
アルミニウム系金属酸化物類粒子としては、ギブサイト(α−Al(OH)3 )、バイアライト(β−Al(OH)3 )、ベーマイト(α−AlO(OH))、ダイアスポア(β−AlO(OH))などから得られる活性アルミナ粒子、α−アルミナや活性アルミナなど、またはこれらを担体として白金族元素を担持させた粒子などが用いられる。
また鉄系金属酸化物類粒子としては、ゲータイト(α−FeOOH)粒子、レピドクロイサイト( γ−FeOOH) 粒子等の含水酸化第二鉄粒子、ヘマタイト(α−Fe2 O3 )粒子、マグへマイト(γ−Fe2 O3 )粒子、マグネタイト(FeOx ・Fe2 O3 、0<x<1)粒子等の酸化鉄粒子などが用いられる。
これらは混合して用いてもよく、例えば、含水酸化第二鉄粒子または酸化鉄粒子にアルミニウムやケイ素の酸化物または水酸化物で被覆させたものなどが用いられる。
The metal oxide particles used in the present invention have an active catalytic function for combustion, that is, an action of generating active oxygen during combustion to promote combustion. In addition to metal oxide, oxides are formed by heating. Including metal hydroxides. Examples of the metal oxide particles include aluminum metal oxides and iron metal oxides.
Examples of the aluminum-based metal oxide particles include gibbsite (α-Al (OH) 3 ), vialite (β-Al (OH) 3 ), boehmite (α-AlO (OH)), diaspore (β-AlO (OH) )), Etc., activated alumina particles, α-alumina, activated alumina, etc., or particles carrying a platinum group element using these as carriers.
In addition, iron-based metal oxide particles include goethite (α-FeOOH) particles, hydrous ferric oxide particles such as lipidoclosite (γ-FeOOH) particles, hematite (α-Fe 2 O 3 ) particles, Iron oxide particles such as hemite (γ-Fe 2 O 3 ) particles and magnetite (FeO x · Fe 2 O 3 , 0 <x <1) particles are used.
These may be used as a mixture, for example, hydrous ferric oxide particles or iron oxide particles coated with an oxide or hydroxide of aluminum or silicon.
金属酸化物類粒子の粒子径は、紡糸性の点から1.5μm以下が好ましく、0.3μm以下がより好ましい。粒子径が1.5μmを超えると繊維径に対して粒子の占める割合が多くなるため、糸切れが生じ易くなり、また紡糸口金中の濾材への目詰まりが発生し易くなる。また金属酸化物類粒子の添加量(または含有量)は、0.05〜5重量%の範囲とするのが好ましく、紡糸性および燃焼促進効果からは0.1〜2重量%の範囲で添加するのがより好ましい。添加濃度が5重量%を超えると紡糸における発煙が多くなったり、紡糸口金表面のポリマー吐出部周辺への汚れ付着などにより糸切れが生じ易くなる。0.05重量%未満では、燃焼促進効果が得られない場合がある。
金属酸化物類粒子の添加方法としては、紡糸する前の樹脂成分に直接添加してもよいが、混練性の点から、例えば、あらかじめベースポリマーに金属酸化物類粒子を約45重量%以下で混練してペレット状にしたマスターバッチを作製し、紡糸する押出工程で、繊維中の金属酸化物類粒子の添加量が設定した添加濃度になるように調整して添加する方法が好ましい。ただし、マスターバッチ中の添加量が低いものを使用すると、熱履歴を受けたポリマーが多く混入されることになるため、ポリマーの粘度低下による糸切れが生じ易くなり、得られる不織布の強伸度が低下する場合がある。
The particle diameter of the metal oxide particles is preferably 1.5 μm or less, more preferably 0.3 μm or less from the viewpoint of spinnability. When the particle diameter exceeds 1.5 μm, the ratio of the particles to the fiber diameter increases, so that yarn breakage is likely to occur, and clogging of the filter medium in the spinneret tends to occur. The addition amount (or content) of the metal oxide particles is preferably in the range of 0.05 to 5% by weight, and is added in the range of 0.1 to 2% by weight from the viewpoint of spinnability and combustion promotion effect. More preferably. When the added concentration exceeds 5% by weight, smoke generation during spinning increases, and yarn breakage is likely to occur due to dirt adhering to the periphery of the polymer discharge portion on the spinneret surface. If it is less than 0.05% by weight, the combustion promoting effect may not be obtained.
As a method for adding the metal oxide particles, the metal oxide particles may be added directly to the resin component before spinning. From the viewpoint of kneadability, for example, the metal oxide particles are previously added to the base polymer at about 45% by weight or less. A master batch prepared by kneading into a pellet is prepared, and a method of adding by adjusting the added concentration of the metal oxide particles in the fiber to a set addition concentration in an extrusion process of spinning is preferable. However, if a low addition amount in the masterbatch is used, a lot of polymer that has undergone thermal history will be mixed in, so yarn breakage is likely to occur due to a decrease in the viscosity of the polymer, and the resulting nonwoven fabric has a high elongation. May decrease.
本発明に用いられる酸化防止剤は、ポリマー押出時等の熱や酸素によって通常起こるポリマーの分解を防止するとともに、金属酸化物類によるポリマーの酸化を防止する作用を有する。該酸化防止剤としては、酸化防止、変色防止または製造安全性の点などの点から、通常ラジカル連鎖禁止剤として使用されているフェノール系の酸化防止剤、または過酸化物分解剤として使用されている硫黄系またはリン系の酸化防止剤が好ましく、これらは単独でまたは組み合わせて用いてもよい。 The antioxidant used in the present invention has an action of preventing the polymer from being decomposed by heat or oxygen at the time of polymer extrusion or the like and preventing the polymer from being oxidized by metal oxides. The antioxidant is used as a phenolic antioxidant or a peroxide decomposing agent, which is usually used as a radical chain inhibitor, from the viewpoint of oxidation prevention, discoloration prevention or production safety. Sulfur-based or phosphorus-based antioxidants are preferable, and these may be used alone or in combination.
フェノール系酸化防止剤としては、例えば、2,6−t−ブチル−4−メチルフェノール、n−オクタデシル−3−(3′、5′−ジ−t−ブチル−4′−ヒドロキシフェニル)プロピオネート、テトラキス〔メチレン−3−(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオネート〕メタン、トリス(3,5−ジ−t−ブチル−4−ヒドロキシベンジル)イソシアヌレート、4,4′−ブチリデンビス−(3−メチル−6−t−ブチルフェノール)、トリエチレングリコール−ビス〔3−(3−t−ブチル−4−ヒドロキシ−5−メチルフェニル)プロピオネート〕、3,9−ビス[ 2−〔3−(3−t−ブチル−4−ヒドロキシ−5−メチルフェニル)プロピオニルオキシ〕−1,1−ジメチルエチル] −2,4,8,10−テトラオキサスピロ〔5,5〕ウンデカン、4,4−チオビス−(2−t−ブチル−5−メチルフェノール)、2,2−メチレンビス−(6−t−ブチル−メチルフェノール)、4、4′−メチレンビス−(2、6−ジ−t−ブチルフェノール)、1,3,5−トリメチル−2,4,6−トリス(3,5−ジ−t−ブチル−4−ヒドロキシベンジル)ベンゼン、1,1,3−トリス(5−t−ブチル−4−ヒドロキシ−2−メチルフェニル)ブタン、1,6−ヘキサンジオール−ビス〔3−(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオネート〕、イソオクチル−3−3−(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオネート、2,4−ビス(n−オクチルチオ)−6−(4−ヒドロキシ−3,5−ジ−t−ブチルアニリノ)−1,3,5−トリアジン、3,5−ジ−t−ブチル−4−ヒドロキシベンジルフォスフォネート−ジエチルエステル、2,2−チオ−ジエチレンビス〔3−(3,5−ジ−ヒドロキシフェニル)プロピオネート〕、2,4−ビス〔(オクチルチオ)メチル〕−o−クレゾール、N,N′−ヘキサメチレンビス(3、5−ジ−t−ブチル−4−ヒドロキシ−ヒドロシンナマミド)、などが用いられる。 Examples of the phenolic antioxidant include 2,6-t-butyl-4-methylphenol, n-octadecyl-3- (3 ′, 5′-di-t-butyl-4′-hydroxyphenyl) propionate, Tetrakis [methylene-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] methane, tris (3,5-di-t-butyl-4-hydroxybenzyl) isocyanurate, 4,4 ' -Butylidenebis- (3-methyl-6-t-butylphenol), triethylene glycol-bis [3- (3-t-butyl-4-hydroxy-5-methylphenyl) propionate], 3,9-bis [2- [3- (3-tert-butyl-4-hydroxy-5-methylphenyl) propionyloxy] -1,1-dimethylethyl] -2,4,8,10- Tetraoxaspiro [5,5] undecane, 4,4-thiobis- (2-tert-butyl-5-methylphenol), 2,2-methylenebis- (6-tert-butyl-methylphenol), 4, 4 ' -Methylenebis- (2,6-di-t-butylphenol), 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene, 1, 1,3-tris (5-t-butyl-4-hydroxy-2-methylphenyl) butane, 1,6-hexanediol-bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) Propionate], isooctyl-3--3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, 2,4-bis (n-octylthio) -6- (4-hydroxy-3,5-di -T Butylanilino) -1,3,5-triazine, 3,5-di-tert-butyl-4-hydroxybenzylphosphonate-diethyl ester, 2,2-thio-diethylenebis [3- (3,5-di- Hydroxyphenyl) propionate], 2,4-bis [(octylthio) methyl] -o-cresol, N, N'-hexamethylenebis (3,5-di-t-butyl-4-hydroxy-hydrocinnamamide) , Etc. are used.
リン系酸化防止剤としては、例えば、トリスノニルフェニルホスファイト、トリス(2,4−ジ−t−ブチルフェニル)ホスファイト、ジステアリルペンタエリスリトールジホスファイト、ビス(2,4−ジ−t−ブチルフェニル)ペンタエリスリトールフォスファイト、ビス(2,6−ジ−t−ブチル−4−メチルフェニル)ペンタエリスリトールフォスファイト、2,2−メチレンビス(4,6−ジ−t−ブチルフェニル)オクチルフォスファイト、テトラキス(2,4−ジ−t−ブチルフェニル)−4,4′−ビフェニレン−ジ−ホスホナイトなどが用いられる。
硫黄系酸化防止剤としては、例えば、ジラウリル−3,3′−チオジプロピオネート、ジミリスチル−3,3′−チオジプロピオネート、ジステアリル−3,3′−チオジプロピオネート、ペンタエリスリトールテトラキス(3−ラウリルチオプロピオネート)などが用いられる。
Examples of phosphorus antioxidants include trisnonylphenyl phosphite, tris (2,4-di-t-butylphenyl) phosphite, distearyl pentaerythritol diphosphite, and bis (2,4-di-t- Butylphenyl) pentaerythritol phosphite, bis (2,6-di-t-butyl-4-methylphenyl) pentaerythritol phosphite, 2,2-methylenebis (4,6-di-t-butylphenyl) octyl phosphite Tetrakis (2,4-di-t-butylphenyl) -4,4'-biphenylene-di-phosphonite is used.
Examples of the sulfur-based antioxidant include dilauryl-3,3′-thiodipropionate, dimyristyl-3,3′-thiodipropionate, distearyl-3,3′-thiodipropionate, pentaerythritol tetrakis (3-laurylthiopropionate) and the like are used.
酸化防止剤の添加量(または含有量)は0.05〜1重量%が好ましく、より好ましくは0.1重量%〜0.5重量%である。添加量が0.05重量%未満では、酸化防止剤としての効果が弱くなり、押出紡糸中にポリマーの粘度低下によって糸切れが生じ、また得られる不織布の強伸度が低下し易い。また添加量が1重量%を超えると紡糸中の発煙が多くなり、紡糸口金表面のポリマー吐出部周辺への汚れ付着などによる糸切れが生じ易い。酸化防止剤は、ポリマーの重合直後またはペレタイズ時に添加してもよく、また金属酸化物類を添加してマスターバッチとする際に添加してもよい。
また、必要に応じて金属酸化物類の活性触媒機能を低下させないものであれば、光安定剤、滑剤、着色剤、制電剤などの他の添加剤も併用可能であり、不織布の後加工における浸透剤などの付与も可能である。
The addition amount (or content) of the antioxidant is preferably 0.05 to 1% by weight, more preferably 0.1% to 0.5% by weight. When the addition amount is less than 0.05% by weight, the effect as an antioxidant is weakened, yarn breakage occurs due to a decrease in the viscosity of the polymer during extrusion spinning, and the strong elongation of the resulting nonwoven fabric tends to decrease. On the other hand, if the amount added exceeds 1% by weight, smoke generation during spinning increases, and yarn breakage due to dirt adhering to the periphery of the polymer discharge portion on the spinneret surface tends to occur. The antioxidant may be added immediately after polymerization of the polymer or during pelletization, or may be added when a metal oxide is added to form a master batch.
In addition, other additives such as light stabilizers, lubricants, colorants, antistatic agents can be used in combination as long as they do not reduce the active catalyst function of the metal oxides as necessary, and post-processing of the nonwoven fabric It is also possible to apply a penetrant or the like.
本発明の易燃焼性不織布は、例えば、使い捨て製品として使用された後に捨てられてごみ焼却炉等で焼却される際に、その燃焼過程において不織布に含まれる金属酸化物類粒子が、加熱により脱水反応等を起こして自発的に活性酸素を生成させて活性触媒機能を発揮する。また該不織布の燃焼とともに、混在する他のごみ等の燃焼を促進させることができ、ダイオキシン類の発生を抑制することにつながる。不織布の燃焼時に発熱量が増加し、燃焼ガス中のベンゼン発生量が少なくなる程または二酸化炭素の発生量が多くなるほど、燃焼効率がよいことを示し、易燃焼性の不織布であることを示す。
不織布の易燃焼性は、例えば、易燃焼性不織布5mgを熱重量分析装置TG(セイコー電子工業社製)により、空気供給量250ml/min、昇温速度10℃/minで熱分解させ、発熱開始から発熱終了までの発熱量または発熱温度を測定し、無添加の不織布の場合と比較することによって評価することができる。この方法において、易燃焼性不織布が、発熱量において無添加の不織布と比較して200μV ・s/mg以上高い場合、または発熱温度において発熱終了温度が無添加の不織布と比較して15℃以上高温となる場合には燃焼促進に有効であると評価することができる。
The easily combustible nonwoven fabric of the present invention is dehydrated by heating, for example, when it is thrown away after being used as a disposable product and incinerated in a waste incinerator or the like, in which the metal oxide particles contained in the nonwoven fabric are heated. The active catalyst function is exhibited by causing a reaction or the like to spontaneously generate active oxygen. Further, along with the burning of the non-woven fabric, it is possible to promote the burning of other wastes and the like, which leads to the suppression of the generation of dioxins. The amount of heat generated during the burning of the nonwoven fabric increases, and the smaller the amount of benzene generated in the combustion gas or the greater the amount of carbon dioxide generated, the better the combustion efficiency, indicating that the nonwoven fabric is easily combustible.
The non-combustibility of the non-woven fabric is, for example, by thermally decomposing 5 mg of the non-combustible non-woven fabric using a thermogravimetric analyzer TG (manufactured by Seiko Denshi Kogyo Co., Ltd.) at an air supply rate of 250 ml / min and a heating rate of 10 ° C./min. It can be evaluated by measuring the heat generation amount or the heat generation temperature from the heat generation to the end of heat generation and comparing it with the case of the non-added nonwoven fabric. In this method, when the flammable nonwoven fabric is 200 μV · s / mg or more higher in calorific value than the non-added nonwoven fabric, or the exothermic end temperature at the exothermic temperature is 15 ° C. or higher higher than that of the additive-free nonwoven fabric. Can be evaluated to be effective in promoting combustion.
以下、本発明を実施例によりさらに詳しく説明するが、本発明はこれらに限定されるものではない。
なお、例中の不織布はスパンボンド法により製造し、得られた不織布の特性の測定および評価は下記のようにして行った。またポリマーの酸化、分解を抑制する効果の評価は、紡糸中の糸切れ回数および不織布の強伸度で比較した。また燃焼促進効果の評価は、燃焼時の発熱量および燃焼時に発生するガス中の二酸化炭素発生比率およびベンゼン発生比率で比較した。
1)紡糸中の糸切れ回数の測定
紡孔数68H、紡孔径0.25mmの紡糸口金を用いて、紡糸温度230℃、孔当り0.9g/minで吐出し、紡糸速度3300m/minで牽引する糸を5分間目視観察し、糸切れ回数を測定した。糸切れ回数が少ない程、ポリマーの酸化、分解が抑制されていると言える。
2)不織布の強伸度の測定
幅3cm、長さ20cmの試験片を、島津製作所製テンシロンを用いて、つかみ幅100mm、試験速度300mm/minで引張試験を行い、縦方向の破断強力および破断伸度を測定した。不織布の強伸度低下が少ない程、ポリマーの酸化、分解が抑制されていると言える。
3)不織布の熱分解時発熱量の測定
得られた不織布5mgを熱重量分析装置TG(セイコー電子工業社製)により、空気供給量250ml/min、昇温速度10℃/minで熱分解させ、発熱開始から発熱終了までの発熱量を読み取った。発熱量が増加する程、加熱され燃焼が促進されるものと言える。
4)不織布の燃焼ガス中の二酸化炭素ガスおよびベンゼンガス発生比率の測定
得られた不織布35mgを石英管中に入れ、酸素供給量200ml/min下で、700℃で4分間燃焼させ、燃焼ガス中の二酸化炭素発生比率およびベンゼン発生比率をガスクロマトグラフにより測定した。燃焼ガス中の二酸化炭素発生比率が増加するほど完全燃焼化が促進され、ダイオキシン類の出発物質のベンゼン発生比率が減少することになり、ダイオキシン類の発生が抑制されると考える。
EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to these.
In addition, the nonwoven fabric in an example was manufactured by the spunbond method, and the measurement and evaluation of the characteristic of the obtained nonwoven fabric were performed as follows. The evaluation of the effect of suppressing the oxidation and decomposition of the polymer was made by comparing the number of yarn breakage during spinning and the strong elongation of the nonwoven fabric. The combustion promotion effect was evaluated by comparing the calorific value during combustion, the carbon dioxide generation ratio and the benzene generation ratio in the gas generated during combustion.
1) Measurement of the number of yarn breaks during spinning Using a spinneret with a number of holes of 68H and a diameter of 0.25mm, the yarn was discharged at a spinning temperature of 230 ° C, 0.9g / min per hole, and pulled at a spinning speed of 3300m / min. The yarn to be checked was visually observed for 5 minutes, and the number of yarn breaks was measured. It can be said that the smaller the number of yarn breaks, the more suppressed the oxidation and decomposition of the polymer.
2) Measurement of strong elongation of nonwoven fabric Tensileon manufactured by Shimadzu Corporation was used to test a specimen having a width of 3 cm and a length of 20 cm at a grip width of 100 mm and a test speed of 300 mm / min. The elongation was measured. It can be said that the smaller the decrease in the strength and elongation of the nonwoven fabric, the more the oxidation and decomposition of the polymer are suppressed.
3) Measurement of calorific value during thermal decomposition of nonwoven fabric 5 mg of the obtained nonwoven fabric was pyrolyzed with a thermogravimetric analyzer TG (manufactured by Seiko Denshi Kogyo Co., Ltd.) at an air supply rate of 250 ml / min and a heating rate of 10 ° C / min. The amount of heat generated from the start of heat generation to the end of heat generation was read. It can be said that as the calorific value increases, it is heated and combustion is promoted.
4) Measurement of carbon dioxide gas and benzene gas generation ratio in combustion gas of nonwoven fabric 35 mg of the obtained nonwoven fabric was put in a quartz tube and burned at 700 ° C. for 4 minutes under an oxygen supply rate of 200 ml / min. The carbon dioxide generation ratio and the benzene generation ratio were measured by gas chromatography. As the carbon dioxide generation ratio in the combustion gas increases, complete combustion is promoted, and the benzene generation ratio of the starting material of dioxins decreases, and the generation of dioxins is considered to be suppressed.
[実施例1]
フェノール系酸化防止剤Irganox1330(チバ・ガイギー社製:1,3,5−トリメチル−2,4,6−トリス(3,5−ジ−t−ブチル−4−ヒドロキシベンジル)ベンゼン)0.08wt%と、リン系酸化防止剤Irgafos168(チバ・ガイギー社製:トリス(2,4−ジ−t−ブチルフェニル)ホスファイト)0.1wt%とをペレタイズ時に添加したポリプロピレン(JIS−K7210の表1の条件で測定したMFR=40)を原料とし、これに、予め、金属酸化物類粒子(粒子径0.24μmのゲータイト(α−FeOOH)粒子)を原料に対して30wt%で添加したマスターバッチを3.3wt%添加しながら、溶融紡糸した。この溶融紡糸は、紡孔数2000H、紡孔径0.25mmの紡糸口金を用い、紡糸温度230℃、孔当り0.9g/minで吐出し、紡糸速度3300m/minで吐出したポリマーを紡糸口金の近傍にて側方から冷却しながら、エアーサッカー等の牽引引取装置で引き取って行った。牽引引取装置を出た糸条は、移動する金網コンベアー上にウェブとして捕集した。このウェブを搬送し、135℃に加熱した部分熱圧着面積率7%のピン柄エンボス/フラットロール間に通し、部分熱圧着し、金属酸化物類粒子の添加濃度1.0wt%、繊度2.8dtex、目付20g/m2 の不織布を得た。
紡糸中の糸切れ回数は皆無であり、不織布の強伸度の低下も見られなかった。得られた不織布のTG測定における熱分解時の発熱量は金属酸化物類粒子無添加の繊維に比べて高い値を示した。また不織布を燃焼させ、燃焼ガス中の二酸化炭素発生比率を測定すると、金属酸化物類粒子無添加の不織布より増加し、ベンゼン発生比率が減少しており、易燃焼性の不織布であることが確認された。これらの結果を表1に示した。
[Example 1]
Phenolic antioxidant Irganox 1330 (Ciba Geigy Corp .: 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene) 0.08 wt% And 0.1 wt% of a phosphorus-based antioxidant Irgafos 168 (manufactured by Ciba-Geigy: Tris (2,4-di-t-butylphenyl) phosphite) during pelletizing (Table 1 of JIS-K7210) MFR = 40) measured under the conditions, and a master batch in which metal oxide particles (goetite (α-FeOOH) particles having a particle diameter of 0.24 μm) were added in advance at 30 wt% with respect to the raw material. Melt spinning was performed while adding 3.3 wt%. In this melt spinning, a spinneret having a spinning hole number of 2000H and a spinning diameter of 0.25 mm was discharged at a spinning temperature of 230 ° C. and 0.9 g / min per hole, and the polymer discharged at a spinning speed of 3300 m / min was used as the spinneret. While cooling from the side in the vicinity, it was picked up by a traction take-up device such as an air soccer. The yarn exiting the tow-pull device was collected as a web on a moving wire mesh conveyor. This web is conveyed and passed between pin pattern embossing / flat rolls having a partial thermocompression area ratio of 7% heated to 135 ° C., and partially thermocompression bonded, with an addition concentration of metal oxide particles of 1.0 wt% and a fineness of 2. A nonwoven fabric having 8 dtex and a basis weight of 20 g / m 2 was obtained.
There was no yarn breakage during spinning, and no decrease in the strength and elongation of the nonwoven fabric was observed. The calorific value at the time of thermal decomposition in the TG measurement of the obtained non-woven fabric was higher than that of the fiber without addition of metal oxide particles. In addition, when the nonwoven fabric is burned and the carbon dioxide generation ratio in the combustion gas is measured, it increases from the nonwoven fabric without the addition of metal oxide particles, and the benzene generation ratio decreases, confirming that it is an easily combustible nonwoven fabric. It was done. These results are shown in Table 1.
[実施例2]
フェノール系酸化防止剤Irganox1010(チバ・ガイギー社製:テトラキス〔メチレン−3−(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)プロピオネート〕メタン)0.1wt%と、リン系酸化防止剤P−EPQ(サンド社製:テトラキス(2,4−ジ−t−ブチルフェニル)−4,4′−ビフェニレン−ジ−ホスホナイト)0.15wt%とをペレタイズ時に添加したポリプロピレン(JIS−K7210の表1の条件で測定したMFR=40)を原料とした以外は実施例1と同様にして、金属酸化物類粒子の添加濃度1.0wt%、繊度2.8dtex、目付20g/m2 の不織布を得た。
紡糸中の糸切れ回数は皆無であり、不織布の強伸度の低下も見られなかった。得られた不織布のTG測定における熱分解時の発熱量は金属酸化物類粒子無添加の繊維に比べて高い値を示した。また不織布を燃焼させ、燃焼ガス中の二酸化炭素発生比率を測定すると、金属酸化物類粒子無添加の不織布より増加し、ベンゼン発生比率が減少しており、易燃焼性の不織布であることが確認された。これらの結果を表1に示した。
[Example 2]
Phenolic antioxidant Irganox 1010 (manufactured by Ciba-Geigy: Tetrakis [methylene-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] methane) 0.1 wt% and phosphorus antioxidant Polypropylene (Table of JIS-K7210) with 0.15 wt% of P-EPQ (Sand Corp .: tetrakis (2,4-di-t-butylphenyl) -4,4′-biphenylene-di-phosphonite) added during pelletization A non-woven fabric having an addition concentration of metal oxide particles of 1.0 wt%, a fineness of 2.8 dtex, and a basis weight of 20 g / m 2 is obtained in the same manner as in Example 1 except that MFR = 40) measured under the conditions of 1 is used as a raw material. Obtained.
There was no yarn breakage during spinning, and no decrease in the strength and elongation of the nonwoven fabric was observed. The calorific value at the time of thermal decomposition in the TG measurement of the obtained non-woven fabric was higher than that of the fiber without addition of metal oxide particles. In addition, when the nonwoven fabric is burned and the carbon dioxide generation ratio in the combustion gas is measured, it increases from the nonwoven fabric without the addition of metal oxide particles, and the benzene generation ratio decreases, confirming that it is an easily combustible nonwoven fabric. It was done. These results are shown in Table 1.
[実施例3]
フェノール系酸化防止剤Irganox1330(チバ・ガイギー社製:1,3,5−トリメチル−2,4,6−トリス(3,5−ジ−t−ブチル−4−ヒドロキシベンジル)ベンゼン)0.20wt%と、リン系酸化防止剤Irgafos168(チバ・ガイギー社製:トリス(2,4−ジ−t−ブチルフェニル)ホスファイト)0.15wt%とをペレタイズ時に添加したポリプロピレン(JIS−K7210の表1の条件で測定したMFR=40)を原料とし、予め、金属酸化物類粒子(粒子径0.9μmの活性アルミナ)を原料に対して15wt%添加したマスターバッチを2wt%添加しながら、溶融紡糸した以外は実施例1と同様にして、金属酸化物類粒子の添加濃度0.3wt%、繊度2.8dtex、目付20g/m2 の不織布を得た。
紡糸中の糸切れ回数は皆無であり、不織布の強伸度の低下も見られなかった。得られた不織布のTG測定における熱分解時の発熱量は金属酸化物類粒子無添加の繊維に比べて高い値を示した。また不織布を燃焼させ、燃焼ガス中の二酸化炭素発生比率を測定すると金属酸化物類粒子無添加の不織布より増加し、ベンゼン発生比率が減少しており、易燃焼性の不織布であることが確認された。これらの結果を表1に示した。
[Example 3]
Phenolic antioxidant Irganox 1330 (Ciba Geigy Corp .: 1,3,5-trimethyl-2,4,6-tris (3,5-di-tert-butyl-4-hydroxybenzyl) benzene) 0.20 wt% And 0.15 wt% of phosphorus-based antioxidant Irgafos 168 (manufactured by Ciba-Geigy: Tris (2,4-di-t-butylphenyl) phosphite) during pelletizing (Table 1 of JIS-K7210) MFR = 40) measured under the conditions was melt-spun while adding 2 wt% of a master batch in which 15 wt% of metal oxide particles (active alumina having a particle diameter of 0.9 μm) was previously added to the raw material. Except for the above, in the same manner as in Example 1, a non-woven fabric having an addition concentration of metal oxide particles of 0.3 wt%, a fineness of 2.8 dtex, and a basis weight of 20 g / m 2 I got a cloth.
There was no yarn breakage during spinning, and no decrease in the strength and elongation of the nonwoven fabric was observed. The calorific value at the time of thermal decomposition in the TG measurement of the obtained non-woven fabric was higher than that of the fiber without addition of metal oxide particles. In addition, when the nonwoven fabric was burned and the carbon dioxide generation ratio in the combustion gas was measured, it increased from the nonwoven fabric without the addition of metal oxide particles, the benzene generation ratio decreased, and it was confirmed that the nonwoven fabric was easily combustible. It was. These results are shown in Table 1.
[実施例4]
フェノール系酸化防止剤Irganox1330(チバ・ガイギー社製:1,3,5−トリメチル−2,4,6−トリス(3,5−ジ−t−ブチル−4−ヒドロキシベンジル)ベンゼン)0.08wt%と、リン系酸化防止剤Irgafos168(チバ・ガイギー社製:トリス(2,4−ジ−t−ブチルフェニル)ホスファイト)0.1wt%とをペレタイズ時に添加したポリプロピレン(JIS−K7210の表1の条件で測定したMFR=40)を原料とし、予め、金属酸化物類粒子(粒子径0.9μmの活性アルミナ)を原料に対して15wt%添加したマスターバッチを2wt%添加しながら、溶融紡糸した以外は実施例1と同様にして、金属酸化物類粒子の添加濃度0.3wt%、繊度2.8dtex、目付20g/m2 の不織布を得た。
紡糸中の糸切れ回数は皆無であり、不織布の強伸度の低下も見られなかった。得られた不織布のTG測定における熱分解時の発熱量は金属酸化物類粒子無添加の繊維に比べて高い値を示した。また不織布を燃焼させ、燃焼ガス中の二酸化炭素発生比率を測定すると金属酸化物類粒子無添加の不織布より増加し、ベンゼン発生比率が減少しており、易燃焼性の不織布であることが確認された。これらの結果を表1に示した。
[Example 4]
Phenolic antioxidant Irganox 1330 (Ciba Geigy Corp .: 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene) 0.08 wt% And 0.1 wt% of a phosphorus-based antioxidant Irgafos 168 (manufactured by Ciba-Geigy: Tris (2,4-di-t-butylphenyl) phosphite) during pelletizing (Table 1 of JIS-K7210) MFR = 40) measured under the conditions was melt-spun while adding 2 wt% of a master batch in which 15 wt% of metal oxide particles (active alumina having a particle diameter of 0.9 μm) was previously added to the raw material. Except for the above, in the same manner as in Example 1, a non-woven fabric having an additive concentration of metal oxide particles of 0.3 wt%, a fineness of 2.8 dtex, and a basis weight of 20 g / m 2 Got.
There was no yarn breakage during spinning, and no decrease in the strength and elongation of the nonwoven fabric was observed. The calorific value at the time of thermal decomposition in the TG measurement of the obtained non-woven fabric was higher than that of the fiber without addition of metal oxide particles. In addition, when the nonwoven fabric was burned and the carbon dioxide generation ratio in the combustion gas was measured, it increased from the nonwoven fabric without the addition of metal oxide particles, the benzene generation ratio decreased, and it was confirmed that the nonwoven fabric was easily combustible. It was. These results are shown in Table 1.
[比較例1]
酸化防止剤を添加しないポリプロピレン(JIS−K7210の表1の条件で測定したMFR=40)を原料とした以外は実施例1と同様にして、溶融紡糸した結果、紡糸中の糸切れ回数は81回/5分間であり、また、不織布を得るのが非常に困難な状態であり、不織布は得られなかった。
[Comparative Example 1]
As a result of melt spinning in the same manner as in Example 1 except that polypropylene (MFR = 40 measured under the conditions of Table 1 of JIS-K7210) without addition of an antioxidant was used as a raw material, the number of yarn breaks during spinning was 81. Times / 5 minutes, and it was very difficult to obtain a nonwoven fabric, and no nonwoven fabric was obtained.
[比較例2]
フェノール系酸化防止剤Irganox1330(チバ・ガイギー社製:1,3,5−トリメチル−2,4,6−トリス(3,5−ジ−t−ブチル−4−ヒドロキシベンジル)ベンゼン)0.01wt%、リン系酸化防止剤Irgafos168(チバ・ガイギー社製:トリス(2,4−ジ−t−ブチルフェニル)ホスファイト)0.02%をペレタイズ時に添加したポリプロピレン(JIS−K7210の表1の条件で測定したMFR=40)を原料とした以外は実施例1と同様にして、金属酸化物類粒子の添加濃度1.0wt%、繊度2.8dtex、目付20g/m2 の不織布を得た。
紡糸中の糸切れ回数は36回/5分間であり、また、不織布を得るのに困難な状態であった。得られた不織布のTG測定における熱分解時の発熱量は金属酸化物類粒子無添加の繊維に比べて高い値を示したが、不織布の強伸度が低下した。
[Comparative Example 2]
Phenolic antioxidant Irganox 1330 (Ciba Geigy Co., Ltd .: 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene) 0.01 wt% In addition, the phosphorus-based antioxidant Irgafos 168 (manufactured by Ciba-Geigy: Tris (2,4-di-t-butylphenyl) phosphite) 0.02% was added during pelletizing under the conditions shown in Table 1 of JIS-K7210. Except that the measured MFR = 40) was used as a raw material, a nonwoven fabric having an addition concentration of metal oxide particles of 1.0 wt%, a fineness of 2.8 dtex, and a basis weight of 20 g / m 2 was obtained in the same manner as in Example 1.
The number of yarn breakage during spinning was 36/5 minutes, and it was difficult to obtain a nonwoven fabric. Although the calorific value at the time of thermal decomposition in the TG measurement of the obtained non-woven fabric showed a higher value than that of the fiber without addition of metal oxide particles, the strength and elongation of the non-woven fabric decreased.
[比較例3]
フェノール系酸化防止剤Irganox1330(チバ・ガイギー社製:1,3,5−トリメチル−2,4,6−トリス(3,5−ジ−t−ブチル−4−ヒドロキシベンジル)ベンゼン)0.08wt%、リン系酸化防止剤Irgafos168(チバ・ガイギー社製:トリス(2,4−ジ−t−ブチルフェニル)ホスファイト)0.1wt%をペレタイズ時に添加したポリプロピレン(JIS−K7210の表1の条件で測定したMFR=40)を原料とし、金属酸化物類粒子を無添加にした以外は、実施例1と同様にして、繊度2.8dtex、目付20g/m2 の不織布を得た。
紡糸中の糸切れ回数は皆無であり、得られた不織布の強伸度の低下は見られなかったが、TG測定における熱分解時の発熱量は、金属酸化物類粒子の添加の繊維に比べて低く、また不織布を燃焼させても、燃焼ガス中の二酸化炭素発生比率は金属酸化物類粒子添加時のような増加はみられず、ベンゼン発生比率の減少はみられなかった。
[Comparative Example 3]
Phenolic antioxidant Irganox 1330 (Ciba Geigy Corp .: 1,3,5-trimethyl-2,4,6-tris (3,5-di-t-butyl-4-hydroxybenzyl) benzene) 0.08 wt% In addition, the phosphorus-based antioxidant Irgafos 168 (manufactured by Ciba-Geigy: Tris (2,4-di-t-butylphenyl) phosphite) 0.1 wt% was added during pelletizing under the conditions shown in Table 1 of JIS-K7210. A non-woven fabric having a fineness of 2.8 dtex and a basis weight of 20 g / m 2 was obtained in the same manner as in Example 1 except that the measured MFR = 40) was used as a raw material and no metal oxide particles were added.
There was no yarn breakage during spinning, and no decrease in the strength and elongation of the obtained nonwoven fabric was observed, but the calorific value during pyrolysis in the TG measurement was higher than that of the fiber added with metal oxide particles. Even when the nonwoven fabric was burned, the carbon dioxide generation ratio in the combustion gas did not increase as when the metal oxide particles were added, and the benzene generation ratio did not decrease.
本発明の易燃焼性不織布は、紡糸性が良好で、焼却時の燃焼性に優れるため、使い捨て素材として、オムツやナプキンなどの衛生材料を始め、ウェットティッシュや生ごみの水切り袋などの生活資材、医療用の簡易マスクやメディカルガウンなどの種々の分野において好適に使用することができ、また使用した後の焼却炉での燃焼の際にダイオキシン類等の有害成分の発生を抑制することができる。
The easily combustible non-woven fabric of the present invention has good spinnability and excellent combustibility during incineration, so as a disposable material, it includes sanitary materials such as diapers and napkins, as well as living materials such as wet tissue and garbage draining bags. Can be suitably used in various fields such as medical simple masks and medical gowns, and can suppress the generation of harmful components such as dioxins during combustion in an incinerator after use. .
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