US20050048272A1 - Low emission fibrous webs and method of such webs - Google Patents
Low emission fibrous webs and method of such webs Download PDFInfo
- Publication number
- US20050048272A1 US20050048272A1 US10/647,917 US64791703A US2005048272A1 US 20050048272 A1 US20050048272 A1 US 20050048272A1 US 64791703 A US64791703 A US 64791703A US 2005048272 A1 US2005048272 A1 US 2005048272A1
- Authority
- US
- United States
- Prior art keywords
- web
- percent
- binder
- bisulfite
- polymer
- 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.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims description 15
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 162
- 239000011230 binding agent Substances 0.000 claims abstract description 74
- 239000004816 latex Substances 0.000 claims abstract description 34
- 229920000126 latex Polymers 0.000 claims abstract description 34
- -1 bisulphite compound Chemical class 0.000 claims abstract description 25
- 229920005594 polymer fiber Polymers 0.000 claims abstract description 24
- 229920000642 polymer Polymers 0.000 claims abstract description 19
- 239000000835 fiber Substances 0.000 claims abstract description 16
- 229920000728 polyester Polymers 0.000 claims abstract description 14
- 239000002952 polymeric resin Substances 0.000 claims abstract description 7
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 7
- 229920005989 resin Polymers 0.000 claims description 29
- 239000011347 resin Substances 0.000 claims description 29
- 238000004519 manufacturing process Methods 0.000 claims description 19
- AOSFMYBATFLTAQ-UHFFFAOYSA-N 1-amino-3-(benzimidazol-1-yl)propan-2-ol Chemical group C1=CC=C2N(CC(O)CN)C=NC2=C1 AOSFMYBATFLTAQ-UHFFFAOYSA-N 0.000 claims description 15
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 9
- 238000001035 drying Methods 0.000 claims description 9
- 229920006243 acrylic copolymer Polymers 0.000 claims description 8
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 4
- 229920001909 styrene-acrylic polymer Polymers 0.000 claims description 4
- 230000006872 improvement Effects 0.000 claims description 3
- 239000000155 melt Substances 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 6
- ZETCGWYACBNPIH-UHFFFAOYSA-N azane;sulfurous acid Chemical compound N.OS(O)=O ZETCGWYACBNPIH-UHFFFAOYSA-N 0.000 abstract 1
- 239000010426 asphalt Substances 0.000 description 11
- 230000008569 process Effects 0.000 description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 239000004202 carbamide Substances 0.000 description 5
- 239000003365 glass fiber Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000002516 radical scavenger Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002174 Styrene-butadiene Substances 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229920001568 phenolic resin Polymers 0.000 description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- LVGQIQHJMRUCRM-UHFFFAOYSA-L calcium bisulfite Chemical compound [Ca+2].OS([O-])=O.OS([O-])=O LVGQIQHJMRUCRM-UHFFFAOYSA-L 0.000 description 2
- 235000010260 calcium hydrogen sulphite Nutrition 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000007849 furan resin Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 1
- LECNYTOLLNCBBO-UHFFFAOYSA-N 2-(carbamoylamino)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCNC(N)=O LECNYTOLLNCBBO-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- MLIREBYILWEBDM-UHFFFAOYSA-M 2-cyanoacetate Chemical compound [O-]C(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-M 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- BBDKZWKEPDTENS-UHFFFAOYSA-N 4-Vinylcyclohexene Chemical compound C=CC1CCC=CC1 BBDKZWKEPDTENS-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical class CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- GCPWJFKTWGFEHH-UHFFFAOYSA-N acetoacetamide Chemical compound CC(=O)CC(N)=O GCPWJFKTWGFEHH-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229920006322 acrylamide copolymer Polymers 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- DGJMPUGMZIKDRO-UHFFFAOYSA-N cyanoacetamide Chemical compound NC(=O)CC#N DGJMPUGMZIKDRO-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction 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
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000013538 functional additive Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/34—Introducing sulfur atoms or sulfur-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
-
- 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
-
- 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
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
- D04H3/12—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with filaments or yarns secured together by chemical or thermo-activatable bonding agents, e.g. adhesives, applied or incorporated in liquid or solid form
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen
- C08L23/0853—Ethene vinyl acetate copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/10—Copolymers of styrene with conjugated dienes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/12—Copolymers of styrene with unsaturated nitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249924—Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
Definitions
- This invention involves webs of polymer fibers containing latex binder modified with formaldehyde containing crosslinkers in which the formaldehyde component is chemically bound and that display substantially reduced formaldehyde emissions during the drying, curing and further processing and storing of the webs.
- the webs of the invention also have good hot strength.
- the invention also involves the method of making polymer fiber webs having substantially lower formaldehyde emissions and substantially lower formaldehyde emissions when later processed at elevated temperatures to produce other products like asphaltic roofing products.
- polymer fibrous mats for use in making asphaltic and modified asphaltic roofing products like roll roofing products by bonding inorganic fibers or polymer together with a latex binder such as an SBR or acrylic type latex containing crosslinking ingredients that emit formaldehyde when dried and cured at an elevated temperature and when later processed with hot asphaltic material to make roofing products, or when subjected to hot, humid conditions.
- a latex binder such as an SBR or acrylic type latex containing crosslinking ingredients that emit formaldehyde when dried and cured at an elevated temperature and when later processed with hot asphaltic material to make roofing products, or when subjected to hot, humid conditions.
- Such ingredients are crosslinking agents employed to improve cured physical binder properties through functional groups, usually incorporated into the latex polymer backbone by copolymerization of N-methylol acrylamide, N-methylol methacrylamide, or the addition of resins that contain N-methylol functional groups that are either chemically blocked or unblocked.
- binders including melamine formaldehyde resin mixed with copolymers of styrene, butadiene, acrylic acid and acrylamide and other catalysts and functional additives have been used as a binder in spunbond roofing webs.
- the resin binders provide Thermal Dimensional Stability to the webs to reduce stretching in the machine direction and cross machine direction shrinkage, necking down, when the webs are impregnated or coated with hot asphalt.
- Such a process and products are disclosed in U.S. Pat. Nos. 3,967,032, 4,125,663.
- a disadvantage of these binders and products is that they emit formaldehyde vapors when heated in the drying and curing operation during manufacturing of the Spunbond webs or by hot asphalt.
- U.S. Pat. No. 5,795,933 also teaches adding a bisulfite such as sodium bisulfite, ammonium bisulfite or calcium bisulfite as a formaldehyde scavenger to an urea extended phenolic resin systems employing amino-group-containing formaldehyde scavengers in the manufacture of glass fiber products like thermal insulation.
- a bisulfite such as sodium bisulfite, ammonium bisulfite or calcium bisulfite
- U.S. Pat. No. 5,160,679 teaches using acetoacetamide as an effective formaldehyde scavenger in the manufacture of wood particleboard and durable press finished fabrics that use urea formaldehyde as a binder.
- U.S. Pat. No. teaches using such formaldehyde scavengers as diethylene glycol, sorbitol, urea, melamine, diazine, triazine, and a water-soluble active methylene compound in the manufacture of durable press finished fabrics and wood particleboard.
- U.S. Pat. No. 5,612,405 teaches glass fiber products bonded with a binder containing an aqueous compatible formaldehyde resin like phenolic resin, an aqueous latex elastomeric polymer like styrene butadiene, ethylene propylene monomer, ethylene propylene-diene terpolymer, etc., an acrylic polymer like copolymers of acrylic acid, methacrylic acid acrylic or methacrylic acid esters from 1-4 carbon atoms, acrylamide polymers or copolymers and esters thereof of from 1-4 carbon atoms, and a formaldehyde scavenger like melamine, guanamine, benzyl guanamine, guanidine, dicyandiamide, and the like.
- an aqueous compatible formaldehyde resin like phenolic resin
- an aqueous latex elastomeric polymer like styrene butadiene
- U.S. Pat. No. 5,719,228 teaches using furan resins to bond glass fibers together to manufacture glass fiber products and to add urea or ammonia as formaldehyde scavengers, but also teach that these known additives produce disadvantages and therefore prefer to prereact an acidic furan resin, a formaldehyde scavenger and a source of reactable formaldehyde with a source of ammonia before spraying the binder onto the glass fibers.
- U.S. Pat. No. 5,795,933 teaches aqueous metal coating compositions comprising a formaldehyde containing resin and a formaldehyde scavenger consisting essentially of an organic compound having at least one active methylene hydrogen and a pKa about 5 to 13.
- U.S. Pat. No. 5,143,954 teaches a low formaldehyde, self-cross linking polymer latex composition for use in making nonwoven products, the composition including one or more very complex and costly formaldehyde scavengers such as N-hydroxyethylethyleneurea, ethyl acetoacetate, 2,4-pentanedione, esters of 2-cyanoacetate, 2-cyanoacetamide, trimethylopropane tricyanoacetate, and the polymerized residue of methacryloxyethyleneurea.
- formaldehyde scavengers such as N-hydroxyethylethyleneurea, ethyl acetoacetate, 2,4-pentanedione, esters of 2-cyanoacetate, 2-cyanoacetamide, trimethylopropane tricyanoacetate, and the polymerized residue of methacryloxyethyleneurea.
- the present invention also includes a nonwoven web of polymer fibers bonded with from about 5 to about 30 wt. percent of a cured binder composition, preferably from about 16 to about 24 wt. percent and most preferably from about 18 to about 22 wt. percent, based on the weight of the web or mat.
- the resin component of the binder is of a type that will emit formaldehyde when exposed to the high temperatures of drying and curing or to hot asphalt conditions, such as resins having reasonably good elasticity such as formaldehyde fortified, styrene-butadiene- acrylonitrile, acrylic and similar type resins.
- the binder is preferably a mixture of copolymers, like GenCryl® 9030 available from Omnova Solutions, Inc.
- the binder can also contain trace amounts of free acrylamide, acrylonitrile, butadiene, formaldehyde, methanol, styrene and 4-vinylcyclohexene.
- the basis weight of the web can be any conventional weight but normally is in the range of about 50 to about 250 gms/sq. meter, more typically about 100-225 and preferably about 150-200, such as about 175 gms/sq. meter.
- the latex may be a polymer composed of ethylene-vinyl acetate copolymer, styrene-acrylic copolymer, vinyl-acrylic copolymer, styrene-butadiene-acrylonitrile copolymer, or acrylic copolymer.
- the web is a spunbonded web of polymer, such as polyester, fibers bound together with a resinous binder except that in place of prior art binders, the binder contains one or more formaldehyde fortified polymer resins that normally emit substantial formaldehyde at high temperatures, but in this invention the binder also contains a bisulfite compound, preferably ammonium bisulfite, added in amounts from at least about 0.75 wt. percent up to about 7.5 wt. percent (dry weight basis of the binder).
- This binder is applied in latex form to the fibrous web after the fibers are made and collected in a known manner and then the wet web is dried and heated to cure the binder in a known manner.
- the resultant nonwoven webs have good hot strength and low formaldehyde emissions and reasonable costs, something not heretofore attainable with these types of formaldehyde containing latex binders.
- the webs of the present invention are useful as substrates in known processes for making various roofing products such as built up roofing products and for other known uses in which polymer fiber webs are used.
- the method of making the inventive webs is also part of the present invention.
- This method comprises melting a polymer, converting the melt to fibers, attenuating the fibers to the desired fiber diameter, collecting the fibers in a random pattern on a collecting surface, applying a formaldehyde containing latex resin binder to the web in an amount that the binder content of the dry web will be in the range of about 5-30 wt. percent, based on the weight of the dry web, and drying the web and curing the resin binder to bond the polymer fibers together to form a nonwoven polymer fiber web, the improvement comprising adding about 0.75-7.5 wt. percent, based on the dry weight of the formaldehyde containing resin, of a bisulfite compound to the latex binder before applying the latex binder to the collected polymer fibers.
- the above inventive binder composition produces webs that reduce formaldehyde emissions by more than 25 percent, preferably at least 50 percent and most preferably about 90 percent, compared to a prior art web bound with the same resin, but not containing the bisulfite addition, when the webs are heated to 200 degrees Centigrade., a temperature expected in the drying and curing operation of manufacturing the web or when subjected to hot asphalt.
- This reduction of formaldehyde allows the use of preferred binding resins that contain formaldehyde while avoiding the need for costly investment in thermal or catalytic incinerators or other emission abatement equipment and their operation in both the web manufacturing plant and in the roofing plants where the webs are used.
- the polymer fiber webs of the present invention can be formed by many known processes for making polymer fiber webs, but a typical preferred process is disclosed in U.S. Pat. No. 4,163,305, which reference is incorporated herein by reference.
- the fibers which can be any known polymer fiber, but are preferably polyester fibers
- the web is passed through a binder applicator section where an aqueous latex binder is applied in any conventional manner in the amount desired.
- the wet, bindered web is then passed through a hot oven to dry the web and to cure the resinous latex binder.
- the binders used to make the webs of the present invention are water-based latexes containing one or more polymer resins and a bisulfite, preferably ammonium bisulfite.
- the bisulfite is present in amounts from about 0.75 wt. percent to about 7.5 wt. percent, based on the dry weight of the resin.
- the bisulfite is added in an aqueous solution in a concentration of about 60 wt. percent, but it can be added in other well known forms so long as it dissolves in the binder latex.
- the resin used is a resin that is a latex polymer composed of ethylene-vinyl acetate copolymer, styrene-acrylic copolymer, vinyl-acrylic copolymer, styrene-butadiene-acrylonitrile copolymer, or acrylic copolymer.
- the various copolymers may be prepared by emulsion polymerization of one or more acrylic ester monomers including ethyl acrylate, methyl acrylate, methyl methacrylate, butyl acrylate, 2-ethyl hexylacrylate, hydroxyethyl acrylate, hydroxypropyl acrylate, and hydroxyethyl methacrylate; acrylamide or substituted acrylamides; butadiene; styrene ; acrylonitrile; vinyl acetate or other vinyl esters; carboxylic acid monomers or ethylenically unsaturated anhydrides which can generate carboxylic acids.
- the latex polymer will have an internal N-methylol crosslinker such as of N-methylol acrylamide, N-methylol methacrylamide, or added resins that contain N-methylol functional groups that are either chemically blocked or unblocked.
- resins all emit significant amounts of formaldehyde when heated to high temperatures, such as the conditions in the drying and curing operation of manufacturing the webs or when contacted with hot, molten asphalt in typical roll roofing (Built-Up- roofing products) manufacturing processes.
- resins are typically fortified SBR, acrylic and resins having similar properties as these resins.
- a preferred resin is known as G-9030 available from Omnova Solutions, Inc. of Chester, S.C. This material is a styrene-butadiene-acrylonitrile type latex having the following characteristics:
- any type of polymer fibers can be used in the webs of the present invention depending upon the desired properties of the webs and the intended applications as is well known to the artisan.
- spunbond polyester fibers are preferred.
- the following examples demonstrate the problems solved by the present invention, some of the preferred embodiments and the most preferred embodiment, and demonstrate only a few of the many possible embodiments of the present invention.
- a polyester spunbonded mat was made in a known manner such as the process described in U.S. Pat. No. 4,125,663, the disclosure hereby incorporated herein by reference, in which the binder used to bond the polyester fibers together was GenCryl® 9000, an emulsified styrene butadiene acrylonitrile copolymer latex binder containing very little formaldehyde, available from Omnova Solutions, Inc. of Chester, S.C. This binder did not contain a bisulfite addition. The binder content was 20 wt. percent in the finished dry mat, based on the weight of the dry mat. The properties of this mat are shown in Table 1 below.
- a second polyester spunbond mat was made in the same process as the mat made in Example 1 above except the binder used was GenCryl® 9030, the high performance mixed polymer latex type binder with a 50 percent concentration in water and available from Omnova Solutions, Inc. This binder is described above in detail.
- the binder content in the mat made in this example was about 18 wt. percent.
- high performance binder is meant that the binder contains N-methylol functionality and as such exhibits improved high temperature performance characteristics when subjected to temperatures of hot asphalt, 200 degrees centigrade. No addition of bisulfite was made to this binder. The properties of this mat are shown in Table 1 below.
- Example 2 Another web was made using the process used in Example 1 except that 2.5 wt. percent of ammonium bisulfite (60% concentration in water), based on the dry weight of the binder, was added to the high performance GenCryl® G-9030 binder containing formaldehyde used in Example 2 above. These properties of this finished mat are compared with the properties of the mats made in Examples 1 and 2 in Table 1. TABLE 1 Properties Example 1 Example 2 Example 3 Binder Content (wt. %) 20 18 18 Basis wt. (gms/sq. meter) 173 174 172 Thickness (mm) 0.95 1.01 1.00 Tenmsile strength (lb./in.) Machine Direction 72 79 75 Cross Machine Dir. 46 44 42 Elongation Machine Direction 31 30 30 Cross Machine Dir.
- Thermal Dimensional Stability is a characteristic that is very important in the use of nonwoven polymer fiber mats in the manufacture of roofing products.
- polymer fiber mats tend to stretch in the machine direction and neck down, shrink, in the cross machine direction when coated or impregnated with hot, molten, asphalt or modified asphalt material. This stretching and particularly the necking down in the cross machine direction requires the use of a wider mat to compensate and to insure the final dimension of the roofing product. Wider mats are often much more costly because the machine making the mats is limited in width and as much as 20-50% productivity can be lost when making a wider mat.
- the test for Thermal Dimensional Stability is as follows. Three test samples measuring 350 mm in the machine direction of the mat and 100 mm in the cross machine direction are cut from the mat with a specimen being taken 100 mm from each side of the mat and the third sample taken from the center portion of the mat. A line is drawn across one surface of each of the samples 50 mm on each side of and parallel to the lengthwise centerline of the sample using a material that will still be visible after heating to 200 degrees C. Each sample is mounted on a stand with a preheated clamp that allows each sample to hang vertically in a furnace with a four kg weight attached to the bottom clamp on the sample to provide stress on the sample similar to the stress on the mat in the roofing product manufacturing process.
- Clamps attaching to each sample are preheated for five minutes at 200 degrees Centigrade in the oven, removed and attached to the samples and placed back into the 200 degree oven for five minutes, then removed and allowed to cool under stress for five minutes.
- the distance between the marks made on each sample is measured as is the width of the sample at the lengthwise centerline and the amount of change calculated.
- the three machine direction results are averaged to give the machine direction percent change and the three width or cross machine direction results are averaged to give the cross machine direction percent change. Values of 1.0% or less are highly desirable.
- the nonwoven web or mat of Example 1 has been used to make roofing products. It has acceptable formaldehyde emissions in the drying and curing section of the web manufacturing process or hot asphalt coating operation, but it produces lower performance in hot elongation in the roofing manufacturing process than desired as indicated by the TDS results, i.e. more than desired stretching in the machine direction and necking down in the cross machine direction.
- the nonwoven mat of Example 2 had about 33% improvement in the TDS test compared to that of Example 1, an acceptable hot strength, but the formaldehyde emissions at elevated temperature was unacceptably high.
- the bisulfite compound is useful up to about 7.5 wt. percent to reduce emissions, but above about 7.5 percent the bisulfite begins to degrade the properties of the webs. While ammonium bisulfite is the preferred additive, the bisulfite can be any bisulfite material such as sodium bisulfite, calcium bisulfite, etc.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Nonwoven Fabrics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
- This invention involves webs of polymer fibers containing latex binder modified with formaldehyde containing crosslinkers in which the formaldehyde component is chemically bound and that display substantially reduced formaldehyde emissions during the drying, curing and further processing and storing of the webs. The webs of the invention also have good hot strength. The invention also involves the method of making polymer fiber webs having substantially lower formaldehyde emissions and substantially lower formaldehyde emissions when later processed at elevated temperatures to produce other products like asphaltic roofing products.
- It is known to make polymer fibrous mats for use in making asphaltic and modified asphaltic roofing products like roll roofing products by bonding inorganic fibers or polymer together with a latex binder such as an SBR or acrylic type latex containing crosslinking ingredients that emit formaldehyde when dried and cured at an elevated temperature and when later processed with hot asphaltic material to make roofing products, or when subjected to hot, humid conditions. Such ingredients are crosslinking agents employed to improve cured physical binder properties through functional groups, usually incorporated into the latex polymer backbone by copolymerization of N-methylol acrylamide, N-methylol methacrylamide, or the addition of resins that contain N-methylol functional groups that are either chemically blocked or unblocked. Also, other binders including melamine formaldehyde resin mixed with copolymers of styrene, butadiene, acrylic acid and acrylamide and other catalysts and functional additives have been used as a binder in spunbond roofing webs. The resin binders provide Thermal Dimensional Stability to the webs to reduce stretching in the machine direction and cross machine direction shrinkage, necking down, when the webs are impregnated or coated with hot asphalt. Such a process and products are disclosed in U.S. Pat. Nos. 3,967,032, 4,125,663. A disadvantage of these binders and products is that they emit formaldehyde vapors when heated in the drying and curing operation during manufacturing of the Spunbond webs or by hot asphalt.
- It is also known to add certain known formaldehyde scavengers to binders containing resins that contain formaldehyde to reduce emissions. U.S. Pat. No. 5,578,371 teaches adding urea, melamine, dicyandiamide and/or 1-10 wt. percent of a water-soluble bisulfite or precursor to urea extended phenol formaldehyde binders in the manufacture of fiber glass insulation products, which products are not later coated or impregnated with hot asphalt.
- U.S. Pat. No. 5,795,933 also teaches adding a bisulfite such as sodium bisulfite, ammonium bisulfite or calcium bisulfite as a formaldehyde scavenger to an urea extended phenolic resin systems employing amino-group-containing formaldehyde scavengers in the manufacture of glass fiber products like thermal insulation.
- U.S. Pat. No. 5,160,679 teaches using acetoacetamide as an effective formaldehyde scavenger in the manufacture of wood particleboard and durable press finished fabrics that use urea formaldehyde as a binder. U.S. Pat. No. teaches using such formaldehyde scavengers as diethylene glycol, sorbitol, urea, melamine, diazine, triazine, and a water-soluble active methylene compound in the manufacture of durable press finished fabrics and wood particleboard.
- U.S. Pat. No. 5,612,405 teaches glass fiber products bonded with a binder containing an aqueous compatible formaldehyde resin like phenolic resin, an aqueous latex elastomeric polymer like styrene butadiene, ethylene propylene monomer, ethylene propylene-diene terpolymer, etc., an acrylic polymer like copolymers of acrylic acid, methacrylic acid acrylic or methacrylic acid esters from 1-4 carbon atoms, acrylamide polymers or copolymers and esters thereof of from 1-4 carbon atoms, and a formaldehyde scavenger like melamine, guanamine, benzyl guanamine, guanidine, dicyandiamide, and the like.
- U.S. Pat. No. 5,719,228 teaches using furan resins to bond glass fibers together to manufacture glass fiber products and to add urea or ammonia as formaldehyde scavengers, but also teach that these known additives produce disadvantages and therefore prefer to prereact an acidic furan resin, a formaldehyde scavenger and a source of reactable formaldehyde with a source of ammonia before spraying the binder onto the glass fibers.
- U.S. Pat. No. 5,795,933 teaches aqueous metal coating compositions comprising a formaldehyde containing resin and a formaldehyde scavenger consisting essentially of an organic compound having at least one active methylene hydrogen and a pKa about 5 to 13.
- U.S. Pat. No. 5,143,954 teaches a low formaldehyde, self-cross linking polymer latex composition for use in making nonwoven products, the composition including one or more very complex and costly formaldehyde scavengers such as N-hydroxyethylethyleneurea, ethyl acetoacetate, 2,4-pentanedione, esters of 2-cyanoacetate, 2-cyanoacetamide, trimethylopropane tricyanoacetate, and the polymerized residue of methacryloxyethyleneurea.
- As the above patents indicate, a tremendous effort has been made to suppress the emissions of formaldehyde from various products containing formaldehyde containing resins as a binder, but as yet no effective solution has been known for achieving a formaldehyde resin bound spunbonded web having low formaldehyde emissions during the drying and curing operation of manufacturing the Spunbond web or when contacted with hot asphalt in the manufacture of roofing and similar products. This is the problem solved by the invention described below.
- The present invention also includes a nonwoven web of polymer fibers bonded with from about 5 to about 30 wt. percent of a cured binder composition, preferably from about 16 to about 24 wt. percent and most preferably from about 18 to about 22 wt. percent, based on the weight of the web or mat. The resin component of the binder is of a type that will emit formaldehyde when exposed to the high temperatures of drying and curing or to hot asphalt conditions, such as resins having reasonably good elasticity such as formaldehyde fortified, styrene-butadiene- acrylonitrile, acrylic and similar type resins. The binder is preferably a mixture of copolymers, like GenCryl® 9030 available from Omnova Solutions, Inc. of Chester, S.C. By fortified is meant that formaldehyde is incorporated into the polymer to provide high temperature strength. The binder can also contain trace amounts of free acrylamide, acrylonitrile, butadiene, formaldehyde, methanol, styrene and 4-vinylcyclohexene. The basis weight of the web can be any conventional weight but normally is in the range of about 50 to about 250 gms/sq. meter, more typically about 100-225 and preferably about 150-200, such as about 175 gms/sq. meter. The latex may be a polymer composed of ethylene-vinyl acetate copolymer, styrene-acrylic copolymer, vinyl-acrylic copolymer, styrene-butadiene-acrylonitrile copolymer, or acrylic copolymer.
- The web is a spunbonded web of polymer, such as polyester, fibers bound together with a resinous binder except that in place of prior art binders, the binder contains one or more formaldehyde fortified polymer resins that normally emit substantial formaldehyde at high temperatures, but in this invention the binder also contains a bisulfite compound, preferably ammonium bisulfite, added in amounts from at least about 0.75 wt. percent up to about 7.5 wt. percent (dry weight basis of the binder). This binder is applied in latex form to the fibrous web after the fibers are made and collected in a known manner and then the wet web is dried and heated to cure the binder in a known manner. The resultant nonwoven webs have good hot strength and low formaldehyde emissions and reasonable costs, something not heretofore attainable with these types of formaldehyde containing latex binders. The webs of the present invention are useful as substrates in known processes for making various roofing products such as built up roofing products and for other known uses in which polymer fiber webs are used.
- The method of making the inventive webs is also part of the present invention. This method comprises melting a polymer, converting the melt to fibers, attenuating the fibers to the desired fiber diameter, collecting the fibers in a random pattern on a collecting surface, applying a formaldehyde containing latex resin binder to the web in an amount that the binder content of the dry web will be in the range of about 5-30 wt. percent, based on the weight of the dry web, and drying the web and curing the resin binder to bond the polymer fibers together to form a nonwoven polymer fiber web, the improvement comprising adding about 0.75-7.5 wt. percent, based on the dry weight of the formaldehyde containing resin, of a bisulfite compound to the latex binder before applying the latex binder to the collected polymer fibers.
- The above inventive binder composition produces webs that reduce formaldehyde emissions by more than 25 percent, preferably at least 50 percent and most preferably about 90 percent, compared to a prior art web bound with the same resin, but not containing the bisulfite addition, when the webs are heated to 200 degrees Centigrade., a temperature expected in the drying and curing operation of manufacturing the web or when subjected to hot asphalt. This reduction of formaldehyde allows the use of preferred binding resins that contain formaldehyde while avoiding the need for costly investment in thermal or catalytic incinerators or other emission abatement equipment and their operation in both the web manufacturing plant and in the roofing plants where the webs are used.
- When the word “about” is used herein it is meant that the amount or condition it modifies can vary some beyond that so long as the advantages of the invention are realized. Practically, there is rarely the time or resources available to very precisely determine the limits of all the parameters of ones invention because to do would require an effort far greater than can be justified at the time the invention is being developed to a commercial reality.
- The skilled artisan understands this and expects that the disclosed results of the invention might extend, at least somewhat, beyond one or more of the limits disclosed. Later, having the benefit of the inventors disclosure and understanding the inventive concept and embodiments disclosed including the best mode known to the inventor, the inventor and others can, without inventive effort, explore beyond the limits disclosed to determine if the invention is realized beyond those limits and, when embodiments are found to be without any unexpected characteristics, those embodiments are within the meaning of the term about as used herein. It is not difficult for the artisan or others to determine whether such an embodiment is either as expected or, because of either a break in the continuity of results or one or more features that are significantly better than reported by the inventor, is surprising and thus an unobvious teaching leading to a further advance in the art.
- The polymer fiber webs of the present invention can be formed by many known processes for making polymer fiber webs, but a typical preferred process is disclosed in U.S. Pat. No. 4,163,305, which reference is incorporated herein by reference. After the fibers, which can be any known polymer fiber, but are preferably polyester fibers, are collected in a nonwoven form on a collection surface such as a permeable conveyor belt or chain, the web is passed through a binder applicator section where an aqueous latex binder is applied in any conventional manner in the amount desired. The wet, bindered web is then passed through a hot oven to dry the web and to cure the resinous latex binder.
- The binders used to make the webs of the present invention are water-based latexes containing one or more polymer resins and a bisulfite, preferably ammonium bisulfite. The bisulfite is present in amounts from about 0.75 wt. percent to about 7.5 wt. percent, based on the dry weight of the resin. Typically the bisulfite is added in an aqueous solution in a concentration of about 60 wt. percent, but it can be added in other well known forms so long as it dissolves in the binder latex.
- The resin used is a resin that is a latex polymer composed of ethylene-vinyl acetate copolymer, styrene-acrylic copolymer, vinyl-acrylic copolymer, styrene-butadiene-acrylonitrile copolymer, or acrylic copolymer. The various copolymers may be prepared by emulsion polymerization of one or more acrylic ester monomers including ethyl acrylate, methyl acrylate, methyl methacrylate, butyl acrylate, 2-ethyl hexylacrylate, hydroxyethyl acrylate, hydroxypropyl acrylate, and hydroxyethyl methacrylate; acrylamide or substituted acrylamides; butadiene; styrene ; acrylonitrile; vinyl acetate or other vinyl esters; carboxylic acid monomers or ethylenically unsaturated anhydrides which can generate carboxylic acids. The latex polymer will have an internal N-methylol crosslinker such as of N-methylol acrylamide, N-methylol methacrylamide, or added resins that contain N-methylol functional groups that are either chemically blocked or unblocked.
- These types of resin all emit significant amounts of formaldehyde when heated to high temperatures, such as the conditions in the drying and curing operation of manufacturing the webs or when contacted with hot, molten asphalt in typical roll roofing (Built-Up-Roofing products) manufacturing processes. These resins are typically fortified SBR, acrylic and resins having similar properties as these resins. A preferred resin is known as G-9030 available from Omnova Solutions, Inc. of Chester, S.C. This material is a styrene-butadiene-acrylonitrile type latex having the following characteristics:
-
- Active solids concentration in water 50%
- Ph—about 7.5
- Specific Gravity—1.08
- Volatile organic content (VOC) <0.1%
- Any type of polymer fibers can be used in the webs of the present invention depending upon the desired properties of the webs and the intended applications as is well known to the artisan. When making webs for use in making roofing products spunbond polyester fibers are preferred. The following examples demonstrate the problems solved by the present invention, some of the preferred embodiments and the most preferred embodiment, and demonstrate only a few of the many possible embodiments of the present invention.
- A polyester spunbonded mat was made in a known manner such as the process described in U.S. Pat. No. 4,125,663, the disclosure hereby incorporated herein by reference, in which the binder used to bond the polyester fibers together was GenCryl® 9000, an emulsified styrene butadiene acrylonitrile copolymer latex binder containing very little formaldehyde, available from Omnova Solutions, Inc. of Chester, S.C. This binder did not contain a bisulfite addition. The binder content was 20 wt. percent in the finished dry mat, based on the weight of the dry mat. The properties of this mat are shown in Table 1 below.
- A second polyester spunbond mat was made in the same process as the mat made in Example 1 above except the binder used was GenCryl® 9030, the high performance mixed polymer latex type binder with a 50 percent concentration in water and available from Omnova Solutions, Inc. This binder is described above in detail. The binder content in the mat made in this example was about 18 wt. percent. By high performance binder is meant that the binder contains N-methylol functionality and as such exhibits improved high temperature performance characteristics when subjected to temperatures of hot asphalt, 200 degrees centigrade. No addition of bisulfite was made to this binder. The properties of this mat are shown in Table 1 below.
- Another web was made using the process used in Example 1 except that 2.5 wt. percent of ammonium bisulfite (60% concentration in water), based on the dry weight of the binder, was added to the high performance GenCryl® G-9030 binder containing formaldehyde used in Example 2 above. These properties of this finished mat are compared with the properties of the mats made in Examples 1 and 2 in Table 1.
TABLE 1 Properties Example 1 Example 2 Example 3 Binder Content (wt. %) 20 18 18 Basis wt. (gms/sq. meter) 173 174 172 Thickness (mm) 0.95 1.01 1.00 Tenmsile strength (lb./in.) Machine Direction 72 79 75 Cross Machine Dir. 46 44 42 Elongation Machine Direction 31 30 30 Cross Machine Dir. 33 34 33 Shrinkage @ 200 deg. C. (%) Machine Direction 0.90 0.93 0.94 Cross Machine Dir. −0.30 −.20 −0.22 Tear Strength (lbs.) Machine Direction 32 32 31 Cross Machine Dir. 23 23 23 TDS* @ 200 deg. C. (%) Machine Direction 1.5 1.0 1.0 Cross Machine Dir. −1.6 −1.2 −1.3 Tube Furnace Emissions 1400 16,333 4628 (ppm formaldehyde)**
*Thermal Dimensional Stability (Description of test given below).
**binder heated to 200 deg. C. and exhaust gas analyzed.
- Thermal Dimensional Stability is a characteristic that is very important in the use of nonwoven polymer fiber mats in the manufacture of roofing products. As discussed above in the background, polymer fiber mats tend to stretch in the machine direction and neck down, shrink, in the cross machine direction when coated or impregnated with hot, molten, asphalt or modified asphalt material. This stretching and particularly the necking down in the cross machine direction requires the use of a wider mat to compensate and to insure the final dimension of the roofing product. Wider mats are often much more costly because the machine making the mats is limited in width and as much as 20-50% productivity can be lost when making a wider mat.
- The test for Thermal Dimensional Stability is as follows. Three test samples measuring 350 mm in the machine direction of the mat and 100 mm in the cross machine direction are cut from the mat with a specimen being taken 100 mm from each side of the mat and the third sample taken from the center portion of the mat. A line is drawn across one surface of each of the samples 50 mm on each side of and parallel to the lengthwise centerline of the sample using a material that will still be visible after heating to 200 degrees C. Each sample is mounted on a stand with a preheated clamp that allows each sample to hang vertically in a furnace with a four kg weight attached to the bottom clamp on the sample to provide stress on the sample similar to the stress on the mat in the roofing product manufacturing process. Clamps attaching to each sample are preheated for five minutes at 200 degrees Centigrade in the oven, removed and attached to the samples and placed back into the 200 degree oven for five minutes, then removed and allowed to cool under stress for five minutes. The distance between the marks made on each sample is measured as is the width of the sample at the lengthwise centerline and the amount of change calculated. The three machine direction results are averaged to give the machine direction percent change and the three width or cross machine direction results are averaged to give the cross machine direction percent change. Values of 1.0% or less are highly desirable.
- The nonwoven web or mat of Example 1 has been used to make roofing products. It has acceptable formaldehyde emissions in the drying and curing section of the web manufacturing process or hot asphalt coating operation, but it produces lower performance in hot elongation in the roofing manufacturing process than desired as indicated by the TDS results, i.e. more than desired stretching in the machine direction and necking down in the cross machine direction. The nonwoven mat of Example 2 had about 33% improvement in the TDS test compared to that of Example 1, an acceptable hot strength, but the formaldehyde emissions at elevated temperature was unacceptably high.
- The addition of a bisulfite is effective in lowering formaldehyde emissions at elevated temperatures in amounts as low as 0.75 wt. percent based on the dry weight of the formaldehyde resin in the latex. Table 2 shows the effect of ammonium bisulfite concentration in the G-9030 latex binder in webs made using the method of Example 3, but varying the amount of ammonium bisulfite addition to the binder before applying the binder latex to the polyester web.
TABLE 2 Amount of Bisulfite Compound Added Tube Furnace Results: 0% 0.75% 1.25% 2.5% 5% Emissions (ppm 16,333 12,000 8085 4630 1265 CH20) - The bisulfite compound is useful up to about 7.5 wt. percent to reduce emissions, but above about 7.5 percent the bisulfite begins to degrade the properties of the webs. While ammonium bisulfite is the preferred additive, the bisulfite can be any bisulfite material such as sodium bisulfite, calcium bisulfite, etc.
- The preferred embodiments described above are only a few of the many embodiments possible as will be readily recognized by a person of ordinary skill in this art given the above disclosure. These and obvious modifications thereof are intended to be included in the following claims.
Claims (19)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/647,917 US20050048272A1 (en) | 2003-08-26 | 2003-08-26 | Low emission fibrous webs and method of such webs |
EP20040019538 EP1510607B1 (en) | 2003-08-26 | 2004-08-18 | Low emission fibrous webs and method of such webs |
DK04019538T DK1510607T3 (en) | 2003-08-26 | 2004-08-18 | Low emission fiber webs and method for making such webs |
DE200460006060 DE602004006060T2 (en) | 2003-08-26 | 2004-08-18 | Low emission nonwoven and process for its production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/647,917 US20050048272A1 (en) | 2003-08-26 | 2003-08-26 | Low emission fibrous webs and method of such webs |
Publications (1)
Publication Number | Publication Date |
---|---|
US20050048272A1 true US20050048272A1 (en) | 2005-03-03 |
Family
ID=34104656
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/647,917 Abandoned US20050048272A1 (en) | 2003-08-26 | 2003-08-26 | Low emission fibrous webs and method of such webs |
Country Status (4)
Country | Link |
---|---|
US (1) | US20050048272A1 (en) |
EP (1) | EP1510607B1 (en) |
DE (1) | DE602004006060T2 (en) |
DK (1) | DK1510607T3 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20110272621A1 (en) * | 2008-10-08 | 2011-11-10 | Saint-Gobain Isover | Process for manufacturing insulation products based on mineral wool, and products obtained |
US20120171457A1 (en) * | 2007-02-19 | 2012-07-05 | 3M Innovative Properties Company | Flexible fibrous material,pollution control device, and methods of making the same |
CN103140350A (en) * | 2010-05-25 | 2013-06-05 | 圣戈班艾德福斯公司 | Mat of polymer fibres containing an acetoacetamide, and its use |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2616336A1 (en) * | 2005-07-27 | 2007-02-01 | Wolfgang Seifert | Method for the production of wood material articles with low emissions of chemical compounds |
US9034970B2 (en) | 2009-08-11 | 2015-05-19 | Johns Manville | Curable fiberglass binder comprising salt of inorganic acid |
US9676954B2 (en) | 2009-08-11 | 2017-06-13 | Johns Manville | Formaldehyde-free binder compositions and methods of making the binders under controlled acidic conditions |
US9604878B2 (en) | 2009-08-11 | 2017-03-28 | Johns Manville | Curable fiberglass binder comprising salt of inorganic acid |
US9365963B2 (en) | 2009-08-11 | 2016-06-14 | Johns Manville | Curable fiberglass binder |
US9994482B2 (en) | 2009-08-11 | 2018-06-12 | Johns Manville | Curable fiberglass binder |
US8651285B2 (en) † | 2009-08-19 | 2014-02-18 | Johns Manville | Performance polymeric fiber webs |
US8708162B2 (en) | 2009-08-19 | 2014-04-29 | Johns Manville | Polymeric fiber webs with binder comprising salt of inorganic acid |
US8651286B2 (en) | 2010-12-15 | 2014-02-18 | Johns Manville | Spunbond polyester mat with binder comprising salt of inorganic acid |
US8708163B2 (en) * | 2010-12-15 | 2014-04-29 | Johns Manville | Spunbond polyester fiber webs |
US9695311B2 (en) | 2012-07-27 | 2017-07-04 | Johns Manville | Formaldehyde-free binder compositions and methods of making the binders |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5143954A (en) * | 1990-11-27 | 1992-09-01 | Rohm And Haas Company | Low-formaldehyde, self-crosslinking polymer latex composition |
US5160679A (en) * | 1989-08-29 | 1992-11-03 | Greene Jack T | Process for making particle board including the use of acetoacetamide as a formaldehyde scavenger |
US5178706A (en) * | 1987-01-23 | 1993-01-12 | Sumitomo Chemical Co., Ltd. | Method of producing thin fiber-reinforced resin sheet |
US5362842A (en) * | 1993-09-10 | 1994-11-08 | Georgia Pacific Resins, Inc. | Urea-formaldehyde resin composition and method of manufacture thereof |
US5446195A (en) * | 1986-09-02 | 1995-08-29 | West Point Pepperell | Water-soluble active methylenes as formaldehyde scavengers |
US5578371A (en) * | 1995-08-25 | 1996-11-26 | Schuller International, Inc. | Phenol/formaldehyde fiberglass binder compositions exhibiting reduced emissions |
US5612405A (en) * | 1992-09-22 | 1997-03-18 | Schuller International, Inc. | Glass fiber binding composition containing latex elastomer and method of reducing fallout from glass fiber compositions |
US5719228A (en) * | 1992-05-19 | 1998-02-17 | Schuller International, Inc. | Glass fiber binding compositions, process of making glass fiber binding compositions, process of binding glass fibers, and glass fiber compositions |
US5795933A (en) * | 1996-12-19 | 1998-08-18 | The Dexter Corporation | Waterborne coating compositions having ultra low formaldehyde concentration |
US5914365A (en) * | 1997-02-06 | 1999-06-22 | Georgia-Pacific Resins, Inc. | Modified urea-formaldehyde binder for making fiber mats |
US5972166A (en) * | 1994-09-21 | 1999-10-26 | Owens Corning Fiberglass Technology, Inc. | Non-woven fiber mat and method for forming same |
US6593420B1 (en) * | 1999-08-10 | 2003-07-15 | Knauf Fiber Glass Gmbh | Fiber glass binder compositions with reduced dusting |
US20040209074A1 (en) * | 2003-04-17 | 2004-10-21 | Georgia-Pacific Gypsum Corporation | Mat faced gypsum board |
US6841039B1 (en) * | 1999-06-04 | 2005-01-11 | Roquette Freres | Composition and method for the production of planar structures, especially structures made of paper or cardboard |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL7704678A (en) * | 1976-05-03 | 1977-11-07 | Hoechst Ag | METHOD OF MANUFACTURING A CARRIER JACKET. |
EP0069267B1 (en) * | 1981-07-01 | 1985-05-08 | BASF Aktiengesellschaft | Process for preparing weather resistant sticky cocondensates |
US5530048A (en) * | 1993-07-29 | 1996-06-25 | Georgia-Pacific Resins, Inc. | Phenolic resins for reinforced composites |
FR2788514B1 (en) * | 1999-01-19 | 2002-04-12 | Saint Gobain Isover | INSULATION PRODUCT, ESPECIALLY THERMAL AND MANUFACTURING METHOD THEREOF |
-
2003
- 2003-08-26 US US10/647,917 patent/US20050048272A1/en not_active Abandoned
-
2004
- 2004-08-18 DE DE200460006060 patent/DE602004006060T2/en not_active Expired - Lifetime
- 2004-08-18 EP EP20040019538 patent/EP1510607B1/en not_active Expired - Lifetime
- 2004-08-18 DK DK04019538T patent/DK1510607T3/en active
Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5446195A (en) * | 1986-09-02 | 1995-08-29 | West Point Pepperell | Water-soluble active methylenes as formaldehyde scavengers |
US5178706A (en) * | 1987-01-23 | 1993-01-12 | Sumitomo Chemical Co., Ltd. | Method of producing thin fiber-reinforced resin sheet |
US5160679A (en) * | 1989-08-29 | 1992-11-03 | Greene Jack T | Process for making particle board including the use of acetoacetamide as a formaldehyde scavenger |
US5143954A (en) * | 1990-11-27 | 1992-09-01 | Rohm And Haas Company | Low-formaldehyde, self-crosslinking polymer latex composition |
US5719228A (en) * | 1992-05-19 | 1998-02-17 | Schuller International, Inc. | Glass fiber binding compositions, process of making glass fiber binding compositions, process of binding glass fibers, and glass fiber compositions |
US5612405A (en) * | 1992-09-22 | 1997-03-18 | Schuller International, Inc. | Glass fiber binding composition containing latex elastomer and method of reducing fallout from glass fiber compositions |
US5362842A (en) * | 1993-09-10 | 1994-11-08 | Georgia Pacific Resins, Inc. | Urea-formaldehyde resin composition and method of manufacture thereof |
US5972166A (en) * | 1994-09-21 | 1999-10-26 | Owens Corning Fiberglass Technology, Inc. | Non-woven fiber mat and method for forming same |
US5578371A (en) * | 1995-08-25 | 1996-11-26 | Schuller International, Inc. | Phenol/formaldehyde fiberglass binder compositions exhibiting reduced emissions |
US5795933A (en) * | 1996-12-19 | 1998-08-18 | The Dexter Corporation | Waterborne coating compositions having ultra low formaldehyde concentration |
US5914365A (en) * | 1997-02-06 | 1999-06-22 | Georgia-Pacific Resins, Inc. | Modified urea-formaldehyde binder for making fiber mats |
US6841039B1 (en) * | 1999-06-04 | 2005-01-11 | Roquette Freres | Composition and method for the production of planar structures, especially structures made of paper or cardboard |
US6593420B1 (en) * | 1999-08-10 | 2003-07-15 | Knauf Fiber Glass Gmbh | Fiber glass binder compositions with reduced dusting |
US20040209074A1 (en) * | 2003-04-17 | 2004-10-21 | Georgia-Pacific Gypsum Corporation | Mat faced gypsum board |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120171457A1 (en) * | 2007-02-19 | 2012-07-05 | 3M Innovative Properties Company | Flexible fibrous material,pollution control device, and methods of making the same |
US20110272621A1 (en) * | 2008-10-08 | 2011-11-10 | Saint-Gobain Isover | Process for manufacturing insulation products based on mineral wool, and products obtained |
CN103140350A (en) * | 2010-05-25 | 2013-06-05 | 圣戈班艾德福斯公司 | Mat of polymer fibres containing an acetoacetamide, and its use |
US20130157028A1 (en) * | 2010-05-25 | 2013-06-20 | Saint-Gobain Adfors | Mat of polymer fibers containing an acetoacetamide and use thereof |
CN103140350B (en) * | 2010-05-25 | 2015-08-12 | 圣戈班艾德福斯公司 | Comprise polymer fibre mat and its purposes of acetoacetamide |
Also Published As
Publication number | Publication date |
---|---|
DE602004006060T2 (en) | 2008-01-03 |
EP1510607B1 (en) | 2007-04-25 |
DE602004006060D1 (en) | 2007-06-06 |
DK1510607T3 (en) | 2007-08-20 |
EP1510607A1 (en) | 2005-03-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1510607B1 (en) | Low emission fibrous webs and method of such webs | |
US6642299B2 (en) | Urea-formaldehyde resin binders containing styrene acrylates and acrylic copolymers | |
US6706147B2 (en) | Process for making fiber mats for materials of construction having improved tear strength | |
US5914365A (en) | Modified urea-formaldehyde binder for making fiber mats | |
DE602004004957T2 (en) | A curable aqueous composition and its use as a nonwoven binder | |
US8222167B2 (en) | Urea-formaldehyde resin binders containing acrylic bi-modal molecular weight solution polymer | |
US5518586A (en) | Method of making a high tear strength glass mat | |
US5804254A (en) | Method for flexibilizing cured urea formaldehyde resin-bound glass fiber nonwovens | |
JP2008542451A (en) | Polyvinyl alcohol-based curable aqueous composition containing no formaldehyde | |
DE10350196A1 (en) | Nonwoven catalyst for glass fibers | |
WO2008045706A1 (en) | Improved urea-formaldehyde resin composition and process for making fiber mats | |
US20080160258A1 (en) | Roofing mat using urea-formaldehyde binder of particular viscosity and surface tension | |
US20040082241A1 (en) | Fiberglass nonwoven binder | |
EP2646483B1 (en) | Grafted polymers derived from itaconic acid | |
US20120245277A1 (en) | Aqueous binders for granular and/or fibrous substrates | |
CA2550500A1 (en) | Fiber mat and process for making same | |
AU2004203555A1 (en) | Curable composition and use as binder | |
US7268091B2 (en) | Fiber mat and process for making same | |
RU2725190C1 (en) | Consolidated textile material using binder, method of production and application thereof | |
US7217671B1 (en) | Fiber mat and process for making same | |
US9962731B2 (en) | Methacrylic acid polymer extended urea-formaldehyde resin composition for making fiberglass products | |
US20030089067A1 (en) | Modified copolymer latex binder | |
JPS61239085A (en) | Production of impregnated paper for filter |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: JONS MANVILLE INTERNATIONAL, INC., COLORADO Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:MIELE, PHILIP FRANCIS;REEL/FRAME:014432/0514 Effective date: 20030822 |
|
AS | Assignment |
Owner name: AGILITY CAPITAL, LLC, CALIFORNIA Free format text: SECURITY AGREEMENT;ASSIGNOR:STORACTIVE, INC.;REEL/FRAME:016958/0041 Effective date: 20051223 |
|
AS | Assignment |
Owner name: STORACTIVE, INC., CALIFORNIA Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:AGILITY CAPITAL, LLC;REEL/FRAME:017251/0604 Effective date: 20060303 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- AFTER EXAMINER'S ANSWER OR BOARD OF APPEALS DECISION |