US20010021735A1 - Binder for non-woven fabric - Google Patents
Binder for non-woven fabric Download PDFInfo
- Publication number
- US20010021735A1 US20010021735A1 US09/792,137 US79213701A US2001021735A1 US 20010021735 A1 US20010021735 A1 US 20010021735A1 US 79213701 A US79213701 A US 79213701A US 2001021735 A1 US2001021735 A1 US 2001021735A1
- Authority
- US
- United States
- Prior art keywords
- phr
- ethylene oxide
- fire
- triblock polymer
- binder composition
- 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.)
- Granted
Links
- 239000011230 binding agent Substances 0.000 title claims abstract description 56
- 239000004745 nonwoven fabric Substances 0.000 title abstract description 9
- 229920000126 latex Polymers 0.000 claims abstract description 104
- 239000004816 latex Substances 0.000 claims abstract description 101
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 62
- 239000003063 flame retardant Substances 0.000 claims abstract description 54
- 239000000203 mixture Substances 0.000 claims abstract description 50
- 229920000642 polymer Polymers 0.000 claims abstract description 49
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000005696 Diammonium phosphate Substances 0.000 claims abstract description 25
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910000388 diammonium phosphate Inorganic materials 0.000 claims abstract description 25
- 235000019838 diammonium phosphate Nutrition 0.000 claims abstract description 25
- 229920003048 styrene butadiene rubber Polymers 0.000 claims abstract description 25
- 239000004094 surface-active agent Substances 0.000 claims abstract description 23
- 239000011152 fibreglass Substances 0.000 claims abstract description 21
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims abstract description 18
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 15
- 239000000194 fatty acid Substances 0.000 claims abstract description 15
- 229930195729 fatty acid Natural products 0.000 claims abstract description 15
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 15
- 239000000344 soap Substances 0.000 claims abstract description 15
- 238000004519 manufacturing process Methods 0.000 claims abstract description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000011159 matrix material Substances 0.000 claims description 16
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 238000001035 drying Methods 0.000 claims description 5
- 239000000835 fiber Substances 0.000 abstract description 15
- 229920000728 polyester Polymers 0.000 abstract description 6
- 229920000742 Cotton Polymers 0.000 abstract description 2
- 229920000297 Rayon Polymers 0.000 abstract description 2
- 238000009472 formulation Methods 0.000 abstract description 2
- 229920001778 nylon Polymers 0.000 abstract description 2
- 239000002964 rayon Substances 0.000 abstract description 2
- -1 cyclic phosphonate esters Chemical class 0.000 description 17
- 229920013620 Pliolite Polymers 0.000 description 8
- 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 7
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 238000007720 emulsion polymerization reaction Methods 0.000 description 6
- 229920001451 polypropylene glycol Polymers 0.000 description 6
- 239000002174 Styrene-butadiene Substances 0.000 description 5
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000011115 styrene butadiene Substances 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- 229920001983 poloxamer Polymers 0.000 description 4
- PQYJRMFWJJONBO-UHFFFAOYSA-N Tris(2,3-dibromopropyl) phosphate Chemical compound BrCC(Br)COP(=O)(OCC(Br)CBr)OCC(Br)CBr PQYJRMFWJJONBO-UHFFFAOYSA-N 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 229920001897 terpolymer Polymers 0.000 description 3
- QEQBMZQFDDDTPN-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy benzenecarboperoxoate Chemical compound CC(C)(C)OOOC(=O)C1=CC=CC=C1 QEQBMZQFDDDTPN-UHFFFAOYSA-N 0.000 description 2
- BLKRGXCGFRXRNQ-SNAWJCMRSA-N (z)-3-carbonoperoxoyl-4,4-dimethylpent-2-enoic acid Chemical compound OC(=O)/C=C(C(C)(C)C)\C(=O)OO BLKRGXCGFRXRNQ-SNAWJCMRSA-N 0.000 description 2
- 0 *OC(=O)CC(C(=O)C1=CC=CC=C1)S(=O)(=O)O[Na] Chemical compound *OC(=O)CC(C(=O)C1=CC=CC=C1)S(=O)(=O)O[Na] 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229910006069 SO3H Inorganic materials 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000002223 garnet Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- WYXIGTJNYDDFFH-UHFFFAOYSA-Q triazanium;borate Chemical compound [NH4+].[NH4+].[NH4+].[O-]B([O-])[O-] WYXIGTJNYDDFFH-UHFFFAOYSA-Q 0.000 description 2
- WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 1
- HSLFISVKRDQEBY-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)cyclohexane Chemical compound CC(C)(C)OOC1(OOC(C)(C)C)CCCCC1 HSLFISVKRDQEBY-UHFFFAOYSA-N 0.000 description 1
- XSZYESUNPWGWFQ-UHFFFAOYSA-N 1-(2-hydroperoxypropan-2-yl)-4-methylcyclohexane Chemical compound CC1CCC(C(C)(C)OO)CC1 XSZYESUNPWGWFQ-UHFFFAOYSA-N 0.000 description 1
- UXKQGJYFPNFUJY-UHFFFAOYSA-N 1-(2-methylbutan-2-yldiazenyl)cyclohexane-1-carbonitrile Chemical compound CCC(C)(C)N=NC1(C#N)CCCCC1 UXKQGJYFPNFUJY-UHFFFAOYSA-N 0.000 description 1
- HQOVXPHOJANJBR-UHFFFAOYSA-N 2,2-bis(tert-butylperoxy)butane Chemical compound CC(C)(C)OOC(C)(CC)OOC(C)(C)C HQOVXPHOJANJBR-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- PYKCEDJHRUUDRK-UHFFFAOYSA-N 2-(tert-butyldiazenyl)-2-methylpropanenitrile Chemical compound CC(C)(C)N=NC(C)(C)C#N PYKCEDJHRUUDRK-UHFFFAOYSA-N 0.000 description 1
- WGUWOLAXPCRPKH-UHFFFAOYSA-N 2-(tert-butyldiazenyl)cyclohexane-1-carbonitrile Chemical compound CC(C)(C)N=NC1CCCCC1C#N WGUWOLAXPCRPKH-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- MKTOIPPVFPJEQO-UHFFFAOYSA-N 4-(3-carboxypropanoylperoxy)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OOC(=O)CCC(O)=O MKTOIPPVFPJEQO-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- ZEWLJSFFUGOIKV-UHFFFAOYSA-N C.C.C.C.C.C.[H]OCCOC(C)COCCO Chemical compound C.C.C.C.C.C.[H]OCCOC(C)COCCO ZEWLJSFFUGOIKV-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920001174 Diethylhydroxylamine Polymers 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000000011 acetone peroxide Substances 0.000 description 1
- 235000019401 acetone peroxide Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000013043 chemical agent Substances 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
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- BSVQJWUUZCXSOL-UHFFFAOYSA-N cyclohexylsulfonyl ethaneperoxoate Chemical compound CC(=O)OOS(=O)(=O)C1CCCCC1 BSVQJWUUZCXSOL-UHFFFAOYSA-N 0.000 description 1
- XJOBOFWTZOKMOH-UHFFFAOYSA-N decanoyl decaneperoxoate Chemical compound CCCCCCCCCC(=O)OOC(=O)CCCCCCCCC XJOBOFWTZOKMOH-UHFFFAOYSA-N 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 description 1
- MZGNSEAPZQGJRB-UHFFFAOYSA-N dimethyldithiocarbamic acid Chemical compound CN(C)C(S)=S MZGNSEAPZQGJRB-UHFFFAOYSA-N 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical class CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- HARQWLDROVMFJE-UHFFFAOYSA-N ethyl 3,3-bis(tert-butylperoxy)butanoate Chemical compound CCOC(=O)CC(C)(OOC(C)(C)C)OOC(C)(C)C HARQWLDROVMFJE-UHFFFAOYSA-N 0.000 description 1
- 239000011953 free-radical catalyst Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- QWVBGCWRHHXMRM-UHFFFAOYSA-N hexadecoxycarbonyloxy hexadecyl carbonate Chemical compound CCCCCCCCCCCCCCCCOC(=O)OOC(=O)OCCCCCCCCCCCCCCCC QWVBGCWRHHXMRM-UHFFFAOYSA-N 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- ZQMHJBXHRFJKOT-UHFFFAOYSA-N methyl 2-[(1-methoxy-2-methyl-1-oxopropan-2-yl)diazenyl]-2-methylpropanoate Chemical compound COC(=O)C(C)(C)N=NC(C)(C)C(=O)OC ZQMHJBXHRFJKOT-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- ASLWPAWFJZFCKF-UHFFFAOYSA-N tris(1,3-dichloropropan-2-yl) phosphate Chemical compound ClCC(CCl)OP(=O)(OC(CCl)CCl)OC(CCl)CCl ASLWPAWFJZFCKF-UHFFFAOYSA-N 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/06—Copolymers with styrene
- C08L9/08—Latex
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
- C03C25/27—Rubber latex
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
- C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
- D04H1/587—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives characterised by the bonding agents used
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
- D04H1/64—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
Definitions
- This invention relates to fire-retardant latices which are useful as binders for manufacturing non-woven fabrics.
- the fire-retardant latex binders of this invention are particularly useful in manufacturing non-woven fiberglass furnace filters.
- Various latex compositions can be used as binders for non-woven fabrics.
- a wide variety of chemical agents can be used in latex binders as fire-retardants.
- tris-(2,3-dibromopropyl) phosphate was once widely used as a flame-retardant in manufacturing children's sleepwear.
- tris-(2,3-dibromopropyl) phosphate is no longer used in such applications because testing has showed that it might be carcinogenic.
- Other flame-retardant compounds that have been developed to replace tris-(2,3-dibromopropyl) phosphate include tris(1,3-dichloroisopropyl) phosphate and a mixture of two cyclic phosphonate esters.
- U.S. Pat. No. 2,036,854 discloses that a mixture of ammonium borate or phosphate with an ammonium halide, such as ammonium bromide, is useful for flame-proofing textile materials.
- U.S. Pat. No. 2,036,854 further reports that the ammonium halide appears to greatly enhance the flame-extinguishing properties of the ammonium borate or phosphate.
- U.S. Pat. No. 2,452,054 discloses the use of diammonium phosphate and ammonium bromide as a flame-retardant for use on cellulosic materials. It is further disclosed in U.S. Pat. No. 3,061,492 that ammonium bromide can be used as a flame-retardant for unsaturated polyester resin compositions.
- U.S. Pat. No. 3,840,488 discloses the use of ammonium bromide and urea as flame-retardant additives for styrene-butadiene rubber (SBR) latex that is used for textile treatment and carpet backing applications.
- SBR styrene-butadiene rubber
- U.S. Pat. No. 3,840,488 further discloses that the utilization of ammonium bromide and urea in such latices has the undesirable effect of reducing the viscosity of the latex.
- the teachings of U.S. Pat. No. 3,840,488 further indicate that this undesirable decrease in the viscosity of the latex can be prevented by the addition of a halo alkyl phosphoric acid or salt.
- U.S. Pat. No. 5,484,839 discloses a flame-retardant natural or synthetic latex which is grafted with ring-halogenated, ethylenically unsaturated aromatic monomers. These grafted latex compositions are reported to be useful as non-woven filter media binders, as backcoatings for woven upholstery and draperies, and in other applications.
- U.S. Pat. No. 4,239,670 appreciates the fact that the addition of some flame-retardant materials, such as diammonium phosphate, to latex can cause the latex to become unstable. U.S. Pat. No. 4,239,670 further notes that such instability can render the latex unsuitable for its intended purpose. U.S. Pat. No. 4,239,670 solves the problem of latex instability caused by the addition of diammonium phosphate by further adding one part by weight of ammonium bromide per part by weight of diammonium phosphate added to the latex.
- the present invention specifically discloses a fire-retardant latex binder composition which is comprised of (1) water, (2) a styrene-butadiene rubber, (3) a fatty acid soap, (4) a sulfonate surfactant, (5) an ethylene oxide/propylene oxide/ethylene oxide triblock polymer, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight of at least 8000, and (6) about 10 phr to about 50 phr of diammonium phosphate.
- This fire-retardant latex binder composition is particularly useful as a binder for manufacturing non-woven fabric.
- the present invention further discloses a process for manufacturing a furnace filter which comprises (I) applying a fire-retardant latex binder composition to a fiberglass matrix to produce a latex-coated fiberglass matrix, wherein the fire-retardant latex binder composition is comprised of (1) water, (2) a styrene-butadiene rubber, (3) a fatty acid soap, (4) a sulfonate surfactant, (5) an ethylene oxide/propylene oxide/ethylene oxide triblock polymer, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight of at least 8000, and (6) about 10 phr to about 50 phr of diammonium phosphate, and (II) drying the latex coated fiberglass matrix to produce the furnace filter.
- a fire-retardant latex binder composition is comprised of (1) water, (2) a styrene-butadiene rubber, (3) a fatty acid soap, (4)
- the fire-retardant latex binder compositions of this invention are made by simply mixing about 10 phr (parts per hundred parts by weight of rubber) to about 50 phr of diammonium phosphate into a styrene-butadiene latex that contains a fatty acid soap, a sulfonate surfactant and an ethylene oxide/propylene oxide/ethylene oxide triblock polymer, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight of at least 8000.
- a latex is manufactured and sold by The Goodyear Tire & Rubber Company under the name Pliolite® 5000C. In most cases, from about 15 phr to about 40 phr of diammonium phosphate will be mixed into the latex.
- Such styrene-butadiene rubbers in the latex is comprised of repeat units which are derived from styrene monomer and 1,3-butadiene rubber.
- Such styrene-butadiene rubbers will typically be comprised of repeat units which are derived from about 1 to about 40 weight percent styrene and about 60 to about 99 weight percent butadiene.
- the styrene-butadiene rubber in the latex will typically contain from about 10 weight percent to about 30 styrene and from about 70 weight percent to about 90 weight percent butadiene.
- the styrene-butadiene rubber in the latex will more preferably contain about 15 weight percent to about 25 weight percent styrene and from about 75 weight percent to about 85 weight percent butadiene.
- the styrene-butadiene rubber latex can be synthesized using a fatty acid soap system and conventional emulsion polymerization techniques.
- emulsion polymerizations generally utilize a charge composition which is comprised of water, styrene monomer, 1,3-butadiene monomer, an initiator and a fatty acid soap.
- Such polymerizations can be conducted over a very wide temperature range from about 0° C. to as high as about 100° C.
- Such emulsion polymerizations are typically conducted at a temperature which is within the range of about 5° C. to about 60° C.
- the fatty acid soap used in such polymerizations may be charged at the outset of the polymerization or may be added incrementally or proportionately as the reaction proceeds. Normally, from about 2 phm (parts by weight per 100 parts by weight of monomer) to about 7 phm of the fatty acid soap will be charged into the polymerization medium. It is typically preferred for the polymerization medium to contain from about 4 phm to about 6 phm of the fatty acid soap.
- the emulsion polymerizations used in synthesizing the styrene-butadiene rubber latex may be initiated using free radical catalysts, ultraviolet light or radiation. To insure a satisfactory polymerization rate, uniformity and a controllable polymerization, free radical initiators are virtually always used to initiate such emulsion polymerizations.
- Free radical initiators which are commonly used include the various peroxygen compounds such as potassium persulfate, ammonium persulfate, benzoyl peroxide, hydrogen peroxide, di-t-butylperoxide, dicumyl peroxide, 2,4-dichlorobenzoyl peroxide, decanoyl peroxide, lauroyl peroxide, cumene hydroperoxide, p-menthane hydroperoxide, t-butylhydroperoxide, acetyl acetone peroxide, methyl ethyl ketone peroxide, succinic acid peroxide, dicetyl peroxydicarbonate, t-butyl peroxyacetate, t-butyl peroxymaleic acid, t-butyl peroxybenzoate, t-butyl peroxymaleic acid, t-butyl peroxybenzoate, acetyl cyclohexyl sulfonyl peroxide
- the emulsion polymerization system used in the synthesis of the latex can be treated at the desired degree of conversion with shortstopping agents, such as hydroquinone or a combination of the sodium salt of N,N-dimethyl dithiocarbamate with N,N-diethyl hydroxylamine.
- shortstopping agents such as hydroquinone or a combination of the sodium salt of N,N-dimethyl dithiocarbamate with N,N-diethyl hydroxylamine.
- Typical stabilizing agents and standard antioxidants can also be added to the latex.
- a sulfonate surfactant from about 0.1 phr to 5 phr of a sulfonate surfactant and from about 0.1 phr to about 4 phr of an ethylene oxide/propylene oxide/ethylene oxide block terpolymer will be added latex. It is typically preferred to add 1 phr to 3 phr of the sulfonate surfactant and 0.4 phr to 2 phr of the ethylene oxide/propylene oxide/ethylene oxide block terpolymer to the styrene-butadiene latex.
- sulfonate surfactants that can be employed include: alkane sulfonates, esters and salts (such as alkylchlorosulfonates) and alkylsulfonates with the general formula:
- R is an alkyl group having from 1 to 20 carbon atoms; sulfonates with intermediate linkages such as ester and ester-linked sulfonates such as those having the formula:
- R is an alkyl group having from 1 to 20 carbon atoms such as dialkyl sulfosuccinates; ester salts with the general formula:
- R is an alkyl group having from 1 to 20 carbon atoms, alkarylsulfonates in which the alkyl groups contain preferably from 10 to 20 carbon atoms (e.g., dodecylbenzenesulfonates, such as sodium dodecylbenzenesulfonate) and alkyl phenol sulfonates.
- alkarylsulfonates in which the alkyl groups contain preferably from 10 to 20 carbon atoms (e.g., dodecylbenzenesulfonates, such as sodium dodecylbenzenesulfonate) and alkyl phenol sulfonates.
- Disulfonated surfactants having the structural formula:
- R represents a linear or branched alkyl group containing from about 6 to about 16 carbon atoms and wherein X represents a metal ion, such as a sodium ion, have proven to be excellent surfactants for making the latex used in the practice of this invention.
- X represents a metal ion, such as a sodium ion
- surfactants are sold by The Dow Chemical Company as DowfaxTM anionic surfactants.
- ethylene oxide/propylene oxide/ethylene oxide triblock polymers that can be used are of the structural formula:
- These triblock polymers will typically have a number average molecular weight of at least 8000.
- the triblock polymer will typically have a number average molecular weight which is within the range of about 10,000 to about 20,000. It is normally preferred for the triblock polymer to have a number average molecular weight which is within the range of 10,500 to 16,000. It is typically more preferred for the triblock polymer to have a number average molecular weight which is within the range of 11,000 to 14,000.
- the polyoxypropylene block in the triblock polymer will typically have a number average molecular weight which is within the range of about 2,000 to about 12,000 and will more typically have a number average molecular weight which is within the range of 2,500 to 8,000.
- the polyoxypropylene block in the triblock polymer will preferably have a number average molecular weight which is within the range of 3,000 to 6,000.
- the polyoxypropylene block in the triblock polymer will more preferably have a number average molecular weight which is within the range of 3,500 to 4,500.
- the polyoxyethylene blocks in the triblock polymer will typically comprise 50 weight percent to 90 weight percent of the total weight of the triblock polymer (the polyoxypropylene blocks will, of course, comprise the remaining 10 weight percent to 50 weight percent of the triblock polymer).
- the polyoxyethylene blocks in the triblock polymer will preferably comprise 60 weight percent to 80 weight percent of the total weight of the triblock polymer with the polyoxypropylene blocks comprising the remaining 20 weight percent to 40 weight percent of the triblock polymer.
- the polyoxyethylene blocks in the triblock polymer will preferably comprise 70 weight percent to 75 weight percent of the total weight of the triblock polymer with the polyoxypropylene blocks comprising the remaining 25 weight percent to 30 weight percent of the triblock polymer.
- the triblock polymer prefferably has a HLB (hydrophilic/lipophilic balance) number which is within the range of about 18 to about 26. It is more preferred for the triblock polymer to have a HLB number which is within the range of 18 to 23.
- Pluronic® F108 surfactant and Pluronic® F127F surfactant are representative examples of ethylene oxide/propylene oxide/ethylene oxide triblock polymers that can be used in making the fire-retardant latex binder compositions of this invention.
- the fire-retardant latex binder compositions of this invention can be employed as a binder for manufacturing a wide variety of non-woven fabrics.
- non-woven fabrics can be manufactured using the fire retardant latex binder formulations of this invention using cotton fibers, polyester fibers, rayon fibers, nylon fibers, cellulosic fibers, fiber glass or various mixtures of such fibers.
- the fire retardant latex binders of this invention are particularly useful in manufacturing fiber glass furnace filters.
- the fire-retardant latex binder compositions of this invention can be applied to substrates in manufacturing non-woven fabrics using any method known in the art.
- the fire-retardant latex binder composition can be applied to unwoven substrate fibers by kiss rolling, knife coating, airless spray or padding.
- the latex binder which has been applied to the fibers needs to be dried or cured.
- This drying step is normally conducted by heating the fibers at an elevated temperature for a short period of time which is sufficient to effect drying and a proper cure.
- the temperature used in the drying step will typically be within the range of about 80° C. to about 160° C. and will more typically be within the range of about 110° C. to about 140° C.
- Fiberglass is typically used in manufacturing furnace filters since the fiber can experience high temperatures during periods of its normal service life.
- the fire-retardant latex binder is normally sprayed onto a fiberglass matrix of the desired size and shape.
- the binder will be applied at a level which is sufficient to penetrate the fiberglass matrix.
- the latex-coated matrix is dried using a conventional procedure. For instance, dry air can be circulated through the latex-coated fiberglass matrix at an elevated temperature which is within the range of about 100° C. to about 150° C.
- a fire-retardant latex binder composition can be made by mixing 25 phr of diammonium phosphate into Pliolite® 5000C styrene-butadiene rubber latex. Then, a non-woven polyester sheet can be manufactured by first passing loose polyester fibers through a garnet sizer and then spraying the non-woven polyester sheet produced in the garnet sizer with the latex containing the diammonium phosphate. Then, the wet non-woven polyester sheet can be slowly passed through an oven at a temperature of 300° F. (149° C.). The dried bonded fiber can then be rolled and packaged.
- one liter of Pliolite® 5000C styrene-butadiene latex is diluted with 4 liters of water and 25 phr of diammonium phosphate is added to the diluted latex.
- the diluted latex solution is then mixed with cellulose paper fiber for application to a substrate. Typically, the mixture is applied to walls or ceilings as insulation.
- the latex and cellulose can be applied to any suitable substrate by using a sprayer.
- the substrate coated with 2-5 cm of insulation coating can then be left to dry at room temperature over a period of about 3 to 7 days. This technique is known as the “cellulose fiber method.”
- a fire-retardant latex binder composition can be made by mixing 40 phr of diammonium phosphate into Pliolite® 5000C styrene-butadiene rubber latex.
- the fire-retardant latex binder composition can then be used in manufacturing furnace filters.
- a fiberglass furnace filter matrix of the desired size and shape is prepared.
- the latex binder composition can be applied with a fly sprayer onto both sides on the non-woven fiberglass matrix at a level of about 25 weight percent (dry weight).
- the latex binder coated fiberglass matrix is dried by passing it through an oven dryer that is maintained at a temperature of about 150° C.
- the furnace filters produced by this technique will have outstanding fire-retardant capacity.
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Abstract
This invention relates to fire retardant latex binders for non-woven fabrics. Non-woven fabrics can be manufactured using the fire retardant latex binder formulations of this invention using cotton fibers, polyester fibers, rayon fibers, nylon fibers, cellulosic fibers, fiber glass or various mixtures of such fibers. The fire retardant latex binders of this invention are particularly useful in manufacturing fiber glass furnace filters. The fire retardant latex binders of this invention are comprised of (1) water, (2) a styrene-butadiene rubber, (3) a fatty acid soap, (4) a sulfonate surfactant, (5) an ethylene oxide/propylene oxide/ethylene oxide triblock polymer, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight of at least 8000, and (6) about 10 phr to about 50 phr of diammonium phosphate.
Description
- This invention relates to fire-retardant latices which are useful as binders for manufacturing non-woven fabrics. The fire-retardant latex binders of this invention are particularly useful in manufacturing non-woven fiberglass furnace filters.
- Various latex compositions can be used as binders for non-woven fabrics. In many applications, it is desirable for the latex binder composition to provide fire-retardant characteristics. For instance, in clothing and household applications, it is normally desirable for the latex employed to contain a fire-retardant material.
- A wide variety of chemical agents can be used in latex binders as fire-retardants. For instance, tris-(2,3-dibromopropyl) phosphate was once widely used as a flame-retardant in manufacturing children's sleepwear. However, tris-(2,3-dibromopropyl) phosphate is no longer used in such applications because testing has showed that it might be carcinogenic. Other flame-retardant compounds that have been developed to replace tris-(2,3-dibromopropyl) phosphate include tris(1,3-dichloroisopropyl) phosphate and a mixture of two cyclic phosphonate esters.
- U.S. Pat. No. 2,036,854 discloses that a mixture of ammonium borate or phosphate with an ammonium halide, such as ammonium bromide, is useful for flame-proofing textile materials. U.S. Pat. No. 2,036,854 further reports that the ammonium halide appears to greatly enhance the flame-extinguishing properties of the ammonium borate or phosphate.
- U.S. Pat. No. 2,452,054 discloses the use of diammonium phosphate and ammonium bromide as a flame-retardant for use on cellulosic materials. It is further disclosed in U.S. Pat. No. 3,061,492 that ammonium bromide can be used as a flame-retardant for unsaturated polyester resin compositions.
- U.S. Pat. No. 3,840,488 discloses the use of ammonium bromide and urea as flame-retardant additives for styrene-butadiene rubber (SBR) latex that is used for textile treatment and carpet backing applications. However, U.S. Pat. No. 3,840,488 further discloses that the utilization of ammonium bromide and urea in such latices has the undesirable effect of reducing the viscosity of the latex. The teachings of U.S. Pat. No. 3,840,488 further indicate that this undesirable decrease in the viscosity of the latex can be prevented by the addition of a halo alkyl phosphoric acid or salt.
- U.S. Pat. No. 5,484,839 discloses a flame-retardant natural or synthetic latex which is grafted with ring-halogenated, ethylenically unsaturated aromatic monomers. These grafted latex compositions are reported to be useful as non-woven filter media binders, as backcoatings for woven upholstery and draperies, and in other applications.
- U.S. Pat. No. 4,239,670 appreciates the fact that the addition of some flame-retardant materials, such as diammonium phosphate, to latex can cause the latex to become unstable. U.S. Pat. No. 4,239,670 further notes that such instability can render the latex unsuitable for its intended purpose. U.S. Pat. No. 4,239,670 solves the problem of latex instability caused by the addition of diammonium phosphate by further adding one part by weight of ammonium bromide per part by weight of diammonium phosphate added to the latex.
- It has been unexpectedly found that the stability of styrene-butadiene rubber latices containing diammonium phosphate can be significantly improved by adding from 0.1 phr (parts per 100 parts by weight of dry rubber) to 5 phr of a sulfonate surfactant and 0.1 phr to 4 phr of an ethylene oxide/propylene oxide/ethylene oxide triblock polymer nonionic surfactant thereto. By utilizing this technique fire-retardant latex binder compositions containing diammonium phosphate can be made without the need to add ammonium bromide to attain a satisfactory level of stability. Since diammonium phosphate can be included in the latex composition, it is not necessary to graft a ring-halogenated, ethylenically unsaturated aromatic monomer onto the latex composition to render it fire-retardant.
- The present invention specifically discloses a fire-retardant latex binder composition which is comprised of (1) water, (2) a styrene-butadiene rubber, (3) a fatty acid soap, (4) a sulfonate surfactant, (5) an ethylene oxide/propylene oxide/ethylene oxide triblock polymer, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight of at least 8000, and (6) about 10 phr to about 50 phr of diammonium phosphate. This fire-retardant latex binder composition is particularly useful as a binder for manufacturing non-woven fabric.
- The present invention further discloses a process for manufacturing a furnace filter which comprises (I) applying a fire-retardant latex binder composition to a fiberglass matrix to produce a latex-coated fiberglass matrix, wherein the fire-retardant latex binder composition is comprised of (1) water, (2) a styrene-butadiene rubber, (3) a fatty acid soap, (4) a sulfonate surfactant, (5) an ethylene oxide/propylene oxide/ethylene oxide triblock polymer, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight of at least 8000, and (6) about 10 phr to about 50 phr of diammonium phosphate, and (II) drying the latex coated fiberglass matrix to produce the furnace filter.
- The fire-retardant latex binder compositions of this invention are made by simply mixing about 10 phr (parts per hundred parts by weight of rubber) to about 50 phr of diammonium phosphate into a styrene-butadiene latex that contains a fatty acid soap, a sulfonate surfactant and an ethylene oxide/propylene oxide/ethylene oxide triblock polymer, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight of at least 8000. Such a latex is manufactured and sold by The Goodyear Tire & Rubber Company under the name Pliolite® 5000C. In most cases, from about 15 phr to about 40 phr of diammonium phosphate will be mixed into the latex.
- Such styrene-butadiene rubbers in the latex is comprised of repeat units which are derived from styrene monomer and 1,3-butadiene rubber. Such styrene-butadiene rubbers will typically be comprised of repeat units which are derived from about 1 to about 40 weight percent styrene and about 60 to about 99 weight percent butadiene. The styrene-butadiene rubber in the latex will typically contain from about 10 weight percent to about 30 styrene and from about 70 weight percent to about 90 weight percent butadiene. The styrene-butadiene rubber in the latex will more preferably contain about 15 weight percent to about 25 weight percent styrene and from about 75 weight percent to about 85 weight percent butadiene.
- The styrene-butadiene rubber latex can be synthesized using a fatty acid soap system and conventional emulsion polymerization techniques. Such emulsion polymerizations generally utilize a charge composition which is comprised of water, styrene monomer, 1,3-butadiene monomer, an initiator and a fatty acid soap. Such polymerizations can be conducted over a very wide temperature range from about 0° C. to as high as about 100° C. Such emulsion polymerizations are typically conducted at a temperature which is within the range of about 5° C. to about 60° C.
- The fatty acid soap used in such polymerizations may be charged at the outset of the polymerization or may be added incrementally or proportionately as the reaction proceeds. Normally, from about 2 phm (parts by weight per 100 parts by weight of monomer) to about 7 phm of the fatty acid soap will be charged into the polymerization medium. It is typically preferred for the polymerization medium to contain from about 4 phm to about 6 phm of the fatty acid soap.
- The emulsion polymerizations used in synthesizing the styrene-butadiene rubber latex may be initiated using free radical catalysts, ultraviolet light or radiation. To insure a satisfactory polymerization rate, uniformity and a controllable polymerization, free radical initiators are virtually always used to initiate such emulsion polymerizations. Free radical initiators which are commonly used include the various peroxygen compounds such as potassium persulfate, ammonium persulfate, benzoyl peroxide, hydrogen peroxide, di-t-butylperoxide, dicumyl peroxide, 2,4-dichlorobenzoyl peroxide, decanoyl peroxide, lauroyl peroxide, cumene hydroperoxide, p-menthane hydroperoxide, t-butylhydroperoxide, acetyl acetone peroxide, methyl ethyl ketone peroxide, succinic acid peroxide, dicetyl peroxydicarbonate, t-butyl peroxyacetate, t-butyl peroxymaleic acid, t-butyl peroxybenzoate, t-butyl peroxymaleic acid, t-butyl peroxybenzoate, acetyl cyclohexyl sulfonyl peroxide, and the like; the various azo compounds such as 2-t-butylazo-2-cyanopropane, dimethyl azodiisobutyrate, azodiisobutyronitrile, 2-t-butylazo-1-cyanocyclohexane, 1-t-amylazo-1-cyanocyclohexane, and the like; the various alkyl perketals, such as 2,2-bis-(t-butylperoxy)butane, ethyl 3,3-bis(t-butylperoxy)butyrate, 1,1-di-(t-butylperoxy)cyclohexane, and the like.
- The emulsion polymerization system used in the synthesis of the latex can be treated at the desired degree of conversion with shortstopping agents, such as hydroquinone or a combination of the sodium salt of N,N-dimethyl dithiocarbamate with N,N-diethyl hydroxylamine. Typical stabilizing agents and standard antioxidants can also be added to the latex.
- In accordance with this invention, from about 0.1 phr to 5 phr of a sulfonate surfactant and from about 0.1 phr to about 4 phr of an ethylene oxide/propylene oxide/ethylene oxide block terpolymer will be added latex. It is typically preferred to add 1 phr to 3 phr of the sulfonate surfactant and 0.4 phr to 2 phr of the ethylene oxide/propylene oxide/ethylene oxide block terpolymer to the styrene-butadiene latex. It is typically more preferred to add 1.5 phr to 2.5 phr of the sulfonate surfactant and 0.8 phr to 1.2 phr of the ethylene oxide/propylene oxide/ethylene oxide block terpolymer to the styrene-butadiene latex.
- Some representative examples of sulfonate surfactants that can be employed include: alkane sulfonates, esters and salts (such as alkylchlorosulfonates) and alkylsulfonates with the general formula:
- RSO3H
- wherein R is an alkyl group having from 1 to 20 carbon atoms; sulfonates with intermediate linkages such as ester and ester-linked sulfonates such as those having the formula:
- RCOOC2H4SO3H
- and
- ROOC—CH2—SO3H
-
- wherein R is an alkyl group having from 1 to 20 carbon atoms, alkarylsulfonates in which the alkyl groups contain preferably from 10 to 20 carbon atoms (e.g., dodecylbenzenesulfonates, such as sodium dodecylbenzenesulfonate) and alkyl phenol sulfonates.
-
- wherein R represents a linear or branched alkyl group containing from about 6 to about 16 carbon atoms and wherein X represents a metal ion, such as a sodium ion, have proven to be excellent surfactants for making the latex used in the practice of this invention. Such surfactants are sold by The Dow Chemical Company as Dowfax™ anionic surfactants.
-
- These triblock polymers will typically have a number average molecular weight of at least 8000. The triblock polymer will typically have a number average molecular weight which is within the range of about 10,000 to about 20,000. It is normally preferred for the triblock polymer to have a number average molecular weight which is within the range of 10,500 to 16,000. It is typically more preferred for the triblock polymer to have a number average molecular weight which is within the range of 11,000 to 14,000.
- The polyoxypropylene block in the triblock polymer will typically have a number average molecular weight which is within the range of about 2,000 to about 12,000 and will more typically have a number average molecular weight which is within the range of 2,500 to 8,000. The polyoxypropylene block in the triblock polymer will preferably have a number average molecular weight which is within the range of 3,000 to 6,000. The polyoxypropylene block in the triblock polymer will more preferably have a number average molecular weight which is within the range of 3,500 to 4,500.
- The polyoxyethylene blocks in the triblock polymer will typically comprise 50 weight percent to 90 weight percent of the total weight of the triblock polymer (the polyoxypropylene blocks will, of course, comprise the remaining 10 weight percent to 50 weight percent of the triblock polymer). The polyoxyethylene blocks in the triblock polymer will preferably comprise 60 weight percent to 80 weight percent of the total weight of the triblock polymer with the polyoxypropylene blocks comprising the remaining 20 weight percent to 40 weight percent of the triblock polymer. The polyoxyethylene blocks in the triblock polymer will preferably comprise 70 weight percent to 75 weight percent of the total weight of the triblock polymer with the polyoxypropylene blocks comprising the remaining 25 weight percent to 30 weight percent of the triblock polymer. It is preferred for the triblock polymer to have a HLB (hydrophilic/lipophilic balance) number which is within the range of about 18 to about 26. It is more preferred for the triblock polymer to have a HLB number which is within the range of 18 to 23. Pluronic® F108 surfactant and Pluronic® F127F surfactant are representative examples of ethylene oxide/propylene oxide/ethylene oxide triblock polymers that can be used in making the fire-retardant latex binder compositions of this invention.
- The fire-retardant latex binder compositions of this invention can be employed as a binder for manufacturing a wide variety of non-woven fabrics. For example, non-woven fabrics can be manufactured using the fire retardant latex binder formulations of this invention using cotton fibers, polyester fibers, rayon fibers, nylon fibers, cellulosic fibers, fiber glass or various mixtures of such fibers. The fire retardant latex binders of this invention are particularly useful in manufacturing fiber glass furnace filters.
- The fire-retardant latex binder compositions of this invention can be applied to substrates in manufacturing non-woven fabrics using any method known in the art. For instance, the fire-retardant latex binder composition can be applied to unwoven substrate fibers by kiss rolling, knife coating, airless spray or padding. Irrespective of which method of application is used, the latex binder which has been applied to the fibers needs to be dried or cured. This drying step is normally conducted by heating the fibers at an elevated temperature for a short period of time which is sufficient to effect drying and a proper cure. The temperature used in the drying step will typically be within the range of about 80° C. to about 160° C. and will more typically be within the range of about 110° C. to about 140° C.
- Fiberglass is typically used in manufacturing furnace filters since the fiber can experience high temperatures during periods of its normal service life. In manufacturing such furnace filters, the fire-retardant latex binder is normally sprayed onto a fiberglass matrix of the desired size and shape. The binder will be applied at a level which is sufficient to penetrate the fiberglass matrix. After the binder has been applied to the fiberglass matrix, the latex-coated matrix is dried using a conventional procedure. For instance, dry air can be circulated through the latex-coated fiberglass matrix at an elevated temperature which is within the range of about 100° C. to about 150° C.
- This invention is illustrated by the following examples which are merely for the purpose of illustration and are not to be regarded as limiting the scope of the invention or the manner in which it can be practiced. Unless specifically indicated otherwise, parts and percentages are given by weight.
- In this experiment, 20 phr of diammonium phosphate was added to a bottle of Pliolite® 5356 styrene-butadiene rubber latex that had previously been diluted with water to a solids content of about 33 percent. The Pliolite® 5356 styrene-butadiene latex used was emulsified with a fatty acid soap, had a bound styrene content of about 23.5 percent, an original solids content of about 70 percent, a Brookfield viscosity of about 1400 cps and had a Mooney viscosity of 100. However, upon the addition of the diammonium phosphate, the latex became unstable and coagulated.
- In this experiment, 2 phr of Dowfax® 8390 sulfonate surfactant and 1 phr of Pluronic® F127P polyoxyethylene-polyoxypropylene-polyoxyethylene nonionic surfactant was added to Pliolite® 8390 styrene-butadiene rubber latex. Then, 20 phr of diammonium phosphate was added to the latex. The latex remained stable and coagulation did not occur.
- In this experiment, 2 phr of Dowfax® 8390 sulfonate surfactant and 1 phr of Pluronic® F127P polyoxyethylene-polyoxypropylene-polyoxyethylene nonionic surfactant was added to Pliolite® 8390 styrene-butadiene rubber latex. Then, 40 phr of diammonium phosphate was added to the latex. The latex remained stable and coagulation did not occur. This experiment shows that the addition of the combination of the sulfonate surfactant and the polyoxyethylene-polyoxypropylene-polyoxyethylene nonionic surfactant caused the latex to remain stable even in the case where the diammonium phosphate was added at a very high level.
- A fire-retardant latex binder composition can be made by mixing 25 phr of diammonium phosphate into Pliolite® 5000C styrene-butadiene rubber latex. Then, a non-woven polyester sheet can be manufactured by first passing loose polyester fibers through a garnet sizer and then spraying the non-woven polyester sheet produced in the garnet sizer with the latex containing the diammonium phosphate. Then, the wet non-woven polyester sheet can be slowly passed through an oven at a temperature of 300° F. (149° C.). The dried bonded fiber can then be rolled and packaged.
- In this example, one liter of Pliolite® 5000C styrene-butadiene latex is diluted with 4 liters of water and 25 phr of diammonium phosphate is added to the diluted latex. The diluted latex solution is then mixed with cellulose paper fiber for application to a substrate. Typically, the mixture is applied to walls or ceilings as insulation. The latex and cellulose can be applied to any suitable substrate by using a sprayer. The substrate coated with 2-5 cm of insulation coating can then be left to dry at room temperature over a period of about 3 to 7 days. This technique is known as the “cellulose fiber method.”
- A fire-retardant latex binder composition can be made by mixing 40 phr of diammonium phosphate into Pliolite® 5000C styrene-butadiene rubber latex. The fire-retardant latex binder composition can then be used in manufacturing furnace filters. In such a procedure, a fiberglass furnace filter matrix of the desired size and shape is prepared. Then, the latex binder composition can be applied with a fly sprayer onto both sides on the non-woven fiberglass matrix at a level of about 25 weight percent (dry weight). Then, the latex binder coated fiberglass matrix is dried by passing it through an oven dryer that is maintained at a temperature of about 150° C. The furnace filters produced by this technique will have outstanding fire-retardant capacity.
- While certain representative embodiments and details have been shown for the purpose of illustrating the subject invention, it will be apparent to those skilled in this art that various changes and modifications can be made therein without departing from the scope of the subject invention.
Claims (21)
1. A fire-retardant latex binder composition which is comprised of (1) water, (2) a styrene-butadiene rubber, (3) a fatty acid soap, (4) a sulfonate surfactant, (5) an ethylene oxide/propylene oxide/ethylene oxide triblock polymer, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight of at least 8000, and (6) about 10 phr to about 50 phr of diammonium phosphate.
2. A fire-retardant latex binder composition as specified in wherein the sulfonate surfactant is present at a level which is within the range of about 0.1 phr to about 5 phr, and wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer is present at a level which is within the range of about 0.1 phr to about 4 phr.
claim 1
3. A fire-retardant latex binder composition as specified in wherein the latex binder composition contains from about 2 phr to about 7 phr of the fatty acid soap.
claim 2
4. A fire-retardant latex binder composition as specified in wherein the styrene-butadiene rubber contains repeat units that are derived from about 10 weight percent to about 30 weight percent styrene and from about 70 weight percent to about 90 weight percent 1,3-butadiene.
claim 3
5. A fire-retardant latex binder composition as specified in wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a propylene oxide block that has a number average molecular weight which is within the range of 2,000 to 12,000.
claim 4
6. A fire-retardant latex binder composition as specified in wherein propylene oxide block in the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a molecular weight that represents from 10 weight percent to 50 weight percent of the total molecular weight of the triblock polymer.
claim 5
7. A fire-retardant latex binder composition as specified in wherein the sulfonate surfactant is present at a level which is within the range of about 1 phr to about 3 phr, and wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer is present at a level which is within the range of about 0.4 phr to about 2 phr.
claim 6
8. A fire-retardant latex binder composition as specified in wherein the latex contains from about 4 phr to about 6 phr of the fatty acid soap.
claim 7
9. A fire-retardant latex binder composition as specified in wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight which is within the range of 10,000 to 20,000.
claim 8
10. A fire-retardant latex binder composition as specified in wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a propylene oxide block that has a number average molecular weight which is within the range of 2,500 to 8,000.
claim 9
11. A fire-retardant latex binder composition as specified in wherein propylene oxide block in the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a molecular weight that represents from 20 weight percent to 40 weight percent of the total molecular weight of the triblock polymer.
claim 10
12. A fire-retardant latex binder composition as specified in wherein the diammonium phosphate is present at a level which is within the range of about 15 phr to about 40 phr.
claim 11
13. A fire-retardant latex binder composition as specified in wherein the sulfonate surfactant is present at a level which is within the range of about 1.5 phr to about 2.5 phr, and wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer is present at a level which is within the range of about 0.8 phr to about 1.2 phr.
claim 12
14. A fire-retardant latex binder composition as specified in wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight which is within the range of 10,500 to 16,000.
claim 13
15. A fire-retardant latex binder composition as specified in wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a propylene oxide block that has a number average molecular weight which is within the range of 3,000 to 6,000.
claim 14
16. A fire-retardant latex binder composition as specified in wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight which is within the range of 11,000 to 14,000.
claim 15
17. A fire-retardant latex binder composition as specified in wherein propylene oxide block in the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a molecular weight that represents from 25 weight percent to 30 weight percent of the total molecular weight of the triblock polymer.
claim 16
18. A fire-retardant latex binder composition as specified in wherein the styrene-butadiene rubber contains repeat units that are derived from about 15 weight percent to about 25 weight percent styrene and from about 75 weight percent to about 85 weight percent 1,3-butadiene.
claim 16
19. A process for manufacturing a furnace filter which comprises (I) applying a fire-retardant latex binder composition to a fiberglass matrix to produce a latex-coated fiberglass matrix, wherein the fire-retardant latex binder composition is comprised of (1) water, (2) a styrene-butadiene rubber, (3) a fatty acid soap, (4) a sulfonate surfactant, (5) an ethylene oxide/propylene oxide/ethylene oxide triblock polymer, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer has a number average molecular weight of at least 8000, and (6) about 10 phr to about 50 phr of diammonium phosphate, and (II) drying the latex-coated fiberglass matrix to produce the furnace filter.
20. A process as specified in wherein the sulfonate surfactant is present at a level which is within the range of about 0.1 phr to about 5 phr, wherein the ethylene oxide/propylene oxide/ethylene oxide triblock polymer is present at a level which is within the range of about 0.1 phr to about 4 phr, wherein the fatty acid soap is present at a level which is within the range of about 2 phr to about 7 phr, and wherein the diammonium phosphate is present at a level which is within the range of about 15 phr to about 40 phr.
claim 19
21. A process as specified in wherein the fire-retardant latex binder composition is sprayed onto the fiberglass matrix and wherein the latex coated fiberglass matrix is dried at a temperature which is within the range of about 110° C. to about 150° C.
claim 20
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/792,137 US6344514B2 (en) | 1999-06-02 | 2001-02-22 | Binder for non-woven fabric |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/324,184 US6242524B1 (en) | 1999-06-02 | 1999-06-02 | Binder for non-woven fabric |
| US09/792,137 US6344514B2 (en) | 1999-06-02 | 2001-02-22 | Binder for non-woven fabric |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/324,184 Division US6242524B1 (en) | 1999-06-02 | 1999-06-02 | Binder for non-woven fabric |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| US20010021735A1 true US20010021735A1 (en) | 2001-09-13 |
| US6344514B2 US6344514B2 (en) | 2002-02-05 |
Family
ID=23262471
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/324,184 Expired - Fee Related US6242524B1 (en) | 1999-06-02 | 1999-06-02 | Binder for non-woven fabric |
| US09/792,137 Expired - Fee Related US6344514B2 (en) | 1999-06-02 | 2001-02-22 | Binder for non-woven fabric |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/324,184 Expired - Fee Related US6242524B1 (en) | 1999-06-02 | 1999-06-02 | Binder for non-woven fabric |
Country Status (2)
| Country | Link |
|---|---|
| US (2) | US6242524B1 (en) |
| GB (1) | GB2350614B (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060021148A1 (en) * | 2004-07-30 | 2006-02-02 | Weller David E Jr | Fiberglass products for reducing the flammability of mattresses |
| WO2007000599A1 (en) * | 2005-06-29 | 2007-01-04 | Manel Torres | Non-woven fabric |
| US20070068101A1 (en) * | 2004-12-09 | 2007-03-29 | Weir Charles R | Panel system for reaction-to-fire test applications |
| US20110030120A1 (en) * | 2009-08-06 | 2011-02-10 | National Kaohsiung Normal University | Detachable solar thermal coat assembly with carbon nanocapsule composite material |
| US20180142094A1 (en) * | 2015-12-10 | 2018-05-24 | Lg Chem, Ltd. | Thermoplastic graft copolymer resin, method of preparing the same, and thermoplastic resin composition including the same |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY125326A (en) * | 1999-06-21 | 2006-07-31 | Nippon A&L Inc | A latex compound for dip molding and a dip-molded product |
| US6749720B2 (en) * | 2001-03-21 | 2004-06-15 | Owens Corning Fiberglas Technology, Inc. | Wet-formed mat applications for cement backerboards |
| DE102004016645A1 (en) * | 2004-03-31 | 2005-10-27 | Basf Ag | Aqueous dispersions with improved ion compatibility and their use in paper coating slips |
| EP1932892B1 (en) * | 2006-12-13 | 2009-10-28 | Scapa France | Wire harnessing tape |
| EP2045303A1 (en) * | 2007-10-05 | 2009-04-08 | Scapa France | Abrasion-resistant adhesive tape |
| FR2960565B1 (en) * | 2010-05-25 | 2012-07-27 | Saint Gobain Technical Fabrics | MATERIAL OF POLYMER FIBERS CONTAINING DIHYDRAZIDE AND USE |
| US20120146297A1 (en) * | 2010-12-08 | 2012-06-14 | Mayer Goyenechea Caballero Juan Antonio | Textile material impregnated with water base solution |
| US10301454B2 (en) | 2010-12-08 | 2019-05-28 | Juan Antonio MAYER GOYENECHEA CABALLERO | Water-based elastomeric composition for impregnating textile material and uses thereof |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB371461A (en) | 1930-12-20 | 1932-04-20 | British Celanese | Improvements in the treatment of filamentary and other products |
| US2452054A (en) | 1944-06-20 | 1948-10-26 | Albi Mfg Co Inc | Fire-retardant composition and process |
| US2917476A (en) * | 1956-04-02 | 1959-12-15 | Dow Chemical Co | Latex-based intumescent coating compositions containing solid plasticizers |
| US3061492A (en) | 1960-09-22 | 1962-10-30 | Robertson Co H H | Flame retardant polyester laminates |
| US3840488A (en) | 1972-08-28 | 1974-10-08 | Union Oil Co | Latex with improved flame resistance and stability |
| DE2705555A1 (en) * | 1977-02-10 | 1978-08-17 | Bayer Ag | STABLE HEAT-SENSITIVE LATEX MIXTURES |
| US4239670A (en) | 1978-09-08 | 1980-12-16 | Witco Chemical Company | Flame retardant latexes |
| US5004562A (en) * | 1989-02-01 | 1991-04-02 | Union Oil Company Of California | Latex/sol or gel systems |
| US5302249A (en) * | 1990-01-25 | 1994-04-12 | Xerox Corporation | Treated papers |
| US5308692A (en) * | 1992-06-26 | 1994-05-03 | Herbert Malarkey Roofing Company | Fire resistant mat |
| MX9307200A (en) | 1992-11-18 | 1994-07-29 | Great Lakes Chemical Corp | GRAPED LATEX COMPOSITIONS OF BROMATED STYRENE RETARDANTS OF FLAMAS. |
| US5859121A (en) * | 1995-07-14 | 1999-01-12 | Bayer Corporation | Concentrated aqueous EO/PO nonionic block copolymer solution |
| US5733964A (en) * | 1996-06-20 | 1998-03-31 | Board Of Regents, The University Of Texas System | Surfactants for heterogeneous processes in liquid or supercritical CO2 |
| AU9018698A (en) * | 1997-08-27 | 1999-03-16 | Dow Chemical Company, The | Syndiotactic vinylaromatic polymerization using multiple reactors in series |
-
1999
- 1999-06-02 US US09/324,184 patent/US6242524B1/en not_active Expired - Fee Related
- 1999-08-09 GB GB9918769A patent/GB2350614B/en not_active Expired - Fee Related
-
2001
- 2001-02-22 US US09/792,137 patent/US6344514B2/en not_active Expired - Fee Related
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060021148A1 (en) * | 2004-07-30 | 2006-02-02 | Weller David E Jr | Fiberglass products for reducing the flammability of mattresses |
| WO2006014859A1 (en) * | 2004-07-30 | 2006-02-09 | Owens Corning | Fiberglass products for reducing the flammability of mattresses |
| US8163664B2 (en) | 2004-07-30 | 2012-04-24 | Owens Corning Intellectual Capital, Llc | Fiberglass products for reducing the flammability of mattresses |
| US20070068101A1 (en) * | 2004-12-09 | 2007-03-29 | Weir Charles R | Panel system for reaction-to-fire test applications |
| WO2007000599A1 (en) * | 2005-06-29 | 2007-01-04 | Manel Torres | Non-woven fabric |
| US8088315B2 (en) | 2005-06-29 | 2012-01-03 | Manuel Torres | Non-woven fabric |
| US20110030120A1 (en) * | 2009-08-06 | 2011-02-10 | National Kaohsiung Normal University | Detachable solar thermal coat assembly with carbon nanocapsule composite material |
| US8370965B2 (en) * | 2009-08-06 | 2013-02-12 | Liang-Yang Lin | Detachable solar thermal coat assembly with carbon nanocapsule composite material |
| US20180142094A1 (en) * | 2015-12-10 | 2018-05-24 | Lg Chem, Ltd. | Thermoplastic graft copolymer resin, method of preparing the same, and thermoplastic resin composition including the same |
| US10450453B2 (en) * | 2015-12-10 | 2019-10-22 | Lg Chem, Ltd. | Thermoplastic graft copolymer resin, method of preparing the same, and thermoplastic resin composition including the same |
Also Published As
| Publication number | Publication date |
|---|---|
| US6242524B1 (en) | 2001-06-05 |
| GB2350614A (en) | 2000-12-06 |
| US6344514B2 (en) | 2002-02-05 |
| GB2350614B (en) | 2002-11-13 |
| GB9918769D0 (en) | 1999-10-13 |
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