SE2230310A1 - A coated solid cellulose foam material - Google Patents
A coated solid cellulose foam materialInfo
- Publication number
- SE2230310A1 SE2230310A1 SE2230310A SE2230310A SE2230310A1 SE 2230310 A1 SE2230310 A1 SE 2230310A1 SE 2230310 A SE2230310 A SE 2230310A SE 2230310 A SE2230310 A SE 2230310A SE 2230310 A1 SE2230310 A1 SE 2230310A1
- Authority
- SE
- Sweden
- Prior art keywords
- foam
- coating
- cellulose
- cellulose foam
- solid
- Prior art date
Links
- 229920002678 cellulose Polymers 0.000 title claims abstract description 228
- 239000001913 cellulose Substances 0.000 title claims abstract description 228
- 239000006261 foam material Substances 0.000 title claims abstract description 43
- 239000007787 solid Substances 0.000 title claims description 107
- 239000006260 foam Substances 0.000 claims abstract description 258
- 238000000576 coating method Methods 0.000 claims abstract description 101
- 239000011248 coating agent Substances 0.000 claims abstract description 97
- 239000011247 coating layer Substances 0.000 claims abstract description 48
- 239000008199 coating composition Substances 0.000 claims abstract description 37
- 238000000034 method Methods 0.000 claims abstract description 37
- 229920003043 Cellulose fiber Polymers 0.000 claims description 42
- 239000004094 surface-active agent Substances 0.000 claims description 36
- 239000010410 layer Substances 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 27
- 238000001035 drying Methods 0.000 claims description 22
- 239000002562 thickening agent Substances 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 19
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 230000002209 hydrophobic effect Effects 0.000 claims description 15
- 239000011236 particulate material Substances 0.000 claims description 10
- 239000007788 liquid Substances 0.000 claims description 7
- 239000005022 packaging material Substances 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 3
- 239000004566 building material Substances 0.000 claims description 2
- 239000011810 insulating material Substances 0.000 claims description 2
- 239000000835 fiber Substances 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 15
- 229920001131 Pulp (paper) Polymers 0.000 description 12
- 238000000151 deposition Methods 0.000 description 11
- 230000035699 permeability Effects 0.000 description 11
- 230000008569 process Effects 0.000 description 11
- 239000011148 porous material Substances 0.000 description 10
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 9
- 239000000654 additive Substances 0.000 description 9
- 239000003945 anionic surfactant Substances 0.000 description 9
- 239000011122 softwood Substances 0.000 description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- 239000001768 carboxy methyl cellulose Substances 0.000 description 8
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 8
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 8
- 229940105329 carboxymethylcellulose Drugs 0.000 description 8
- 230000008021 deposition Effects 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- -1 polyethylene Polymers 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- 239000007789 gas Substances 0.000 description 6
- 239000011121 hardwood Substances 0.000 description 5
- 238000004806 packaging method and process Methods 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 238000004537 pulping Methods 0.000 description 5
- 238000004064 recycling Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 238000005273 aeration Methods 0.000 description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 230000003247 decreasing effect Effects 0.000 description 4
- 239000002655 kraft paper Substances 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- 229920000136 polysorbate Polymers 0.000 description 4
- ZUFONQSOSYEWCN-UHFFFAOYSA-M sodium;2-(methylamino)acetate Chemical compound [Na+].CNCC([O-])=O ZUFONQSOSYEWCN-UHFFFAOYSA-M 0.000 description 4
- 239000002023 wood Substances 0.000 description 4
- 229920000875 Dissolving pulp Polymers 0.000 description 3
- 229920002488 Hemicellulose Polymers 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 239000012790 adhesive layer Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 229920005610 lignin Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 2
- 235000017491 Bambusa tulda Nutrition 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 229920000896 Ethulose Polymers 0.000 description 2
- 239000001859 Ethyl hydroxyethyl cellulose Substances 0.000 description 2
- 241000219146 Gossypium Species 0.000 description 2
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- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 240000006240 Linum usitatissimum Species 0.000 description 2
- 235000004431 Linum usitatissimum Nutrition 0.000 description 2
- 244000082204 Phyllostachys viridis Species 0.000 description 2
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000011425 bamboo Substances 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 2
- 229940073507 cocamidopropyl betaine Drugs 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 239000004627 regenerated cellulose Substances 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 238000007761 roller coating Methods 0.000 description 2
- 108700004121 sarkosyl Proteins 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229940045885 sodium lauroyl sarcosinate Drugs 0.000 description 2
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 1
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 241000609240 Ambelania acida Species 0.000 description 1
- 244000180278 Copernicia prunifera Species 0.000 description 1
- 235000010919 Copernicia prunifera Nutrition 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 244000166124 Eucalyptus globulus Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 108010068370 Glutens Proteins 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 229920000433 Lyocell Polymers 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229930182475 S-glycoside Natural products 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 229920002000 Xyloglucan Polymers 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 229940092738 beeswax Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229920013724 bio-based polymer Polymers 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 230000001680 brushing effect Effects 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
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 206010061592 cardiac fibrillation Diseases 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- SFNALCNOMXIBKG-UHFFFAOYSA-N ethylene glycol monododecyl ether Chemical compound CCCCCCCCCCCCOCCO SFNALCNOMXIBKG-UHFFFAOYSA-N 0.000 description 1
- 239000004794 expanded polystyrene Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000021312 gluten Nutrition 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000016507 interphase Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- LAPRIVJANDLWOK-UHFFFAOYSA-N laureth-5 Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCO LAPRIVJANDLWOK-UHFFFAOYSA-N 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methyl-cyclopentane Natural products CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- YYELLDKEOUKVIQ-UHFFFAOYSA-N octaethyleneglycol monododecyl ether Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCO YYELLDKEOUKVIQ-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000012858 packaging process Methods 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- ONQDVAFWWYYXHM-UHFFFAOYSA-M potassium lauryl sulfate Chemical compound [K+].CCCCCCCCCCCCOS([O-])(=O)=O ONQDVAFWWYYXHM-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
- JHJUUEHSAZXEEO-UHFFFAOYSA-M sodium;4-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 JHJUUEHSAZXEEO-UHFFFAOYSA-M 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- ZTUXEFFFLOVXQE-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCC(O)=O ZTUXEFFFLOVXQE-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/18—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B29/00—Layered products comprising a layer of paper or cardboard
- B32B29/002—Layered products comprising a layer of paper or cardboard as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B29/005—Layered products comprising a layer of paper or cardboard as the main or only constituent of a layer, which is next to another layer of the same or of a different material next to another layer of paper or cardboard layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D81/00—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
- B65D81/02—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents specially adapted to protect contents from mechanical damage
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/10—Coatings without pigments
- D21H19/14—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
- D21H19/34—Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising cellulose or derivatives thereof
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/52—Cellulose; Derivatives thereof
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/50—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by form
- D21H21/56—Foam
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
- D21H27/10—Packing paper
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/72—Density
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2439/00—Containers; Receptacles
- B32B2439/70—Food packaging
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2301/00—Characterised by the use of cellulose, modified cellulose or cellulose derivatives
- C08J2301/02—Cellulose; Modified cellulose
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2401/00—Characterised by the use of cellulose, modified cellulose or cellulose derivatives
- C08J2401/02—Cellulose; Modified cellulose
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0085—Use of fibrous compounding ingredients
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/30—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by mixing gases into liquid compositions or plastisols, e.g. frothing with air
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/36—After-treatment
- C08J9/365—Coating
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Abstract
The present invention relates to a coated cellulose foam material having a density in the range of from 10 to 80 kg/m3, and a method for coating a cellulose foam. Said coated cellulose foam material is formed by applying at least one coating layer of at least one coating composition on at least one outer surface of a cellulose foam.
Description
A COATED SOLID CELLULOSE FOAM MATERIAL Field of the invention The present invention relates to a coated solid cellulose foam material and a method for coating a cellulose foam that is at least partially dry.
Background Different porous materials, such as foams, are commonly used in applications such as insulation in buildings and airplanes and as packaging materials that are used to protect various goods during storage and transportation.
Depending on the item to be protected, different types of protective packaging materials can be used. For many items, a low-weight cushioning material that reduces impact shock and vibrations is used. Common examples of such cushioning material are petroleum-based polymer foams such as polyurethane, polyethylene and expanded polystyrene. The foams used should be low-weight, stable and easy to manufacture.
Today, there is an increasing interest in replacing petroleum-based polymers with polymers from renewable resources, i.e. biobased polymers. Cellulose is the most abundant renewable natural polymer on earth and is therefore of special interest.
For a cellulose foam recycling of the material in regular recycling streams may be possible, depending on the composition of the foam.
There are several examples of cellulose foams, prepared using different methods. Drying the wet foam composition is typically a critical step. Since the stability of the wet foam is typically low, moulds are commonly used to prevent the foam from collapsing during drying. WO20200011587 A1 describes a porous material that is prepared by aerating a paste comprising cellulose fibres and gluten and depositing the aerated paste in a mould where it is dried. The dried porous material has the shape of the mould. WO2015036659 A1 describes a moulded fibrous product prepared by foaming an aqueous suspension of natural fibres in combination with synthetic fibres and surfactant, feeding the fibrous foam to a mould and drying the foam by first mechanically withdrawing a part of the water followed by evaporating water to produce a dry fibrous product.
To enable a more versatile and efficient processing, foams that are dimensionally stable already in the wet state are desired.
When replacing foams from petroleum-based polymers with e.g. cellulose foams, there are a number of challenges related to manufacturing processes that must be OVGFCOmG.
For commercially available foams made from petroleum-based polymers, automated foam production and packaging lines use two main means of lifting and moving products, namely pins and vacuum suction. The former entails a movable arm having several metal pins that can be inserted into the foam at an angle, allowing the machine to lift the foam. The pin process leaves small holes in the product, where size depends on the gauge thickness of the pin. The pins need to be sufficiently thick as to not risk breaking, leaving behind metal residue inside the product. Another common method for lifting is vacuum suction, whereby suction cups are pressed against the surface of the foam and air is evacuated. This process relies heavily on having a low air permeable surface in order to generate a vacuum suction and sufficient lift. Furthermore, certain converting equipment such as plotting tables rely on vacuum from below to hold samples in place while cutting. ln these applications it is highly important that the samples do not move since this will break the oscillating blade.
Since cellulose foams generally have a high air permeability due to the porous structure of the foam, it is not possible to use vacuum lifting or fixating equipment during production and converting operations.
Another drawback with cellulose foams is that the surface characteristics of the foam in terms of smoothness does not compare to conventional paper making, where the material is pressed to generate a very smooth surface. The surface texture of the cellulose foam is obtained by the self-consolidation of fibres upon drying. Furthermore, the low-density and porous nature of the cellulose foam presents plenty of capillary action for water to diffuse into, leading to ink bleeding when printing and a lower fidelity print as a result. Lastly, the high moisture uptake of the cellulose foam due to its fibrous and porous nature can present difficulties to deal with condensation of water when used in thermal packaging of frozen goods.
Thus, there is still need for a biobased foam that is recyclable and that also enables use of automated processes including vacuum lifting and fixating equipment. To facilitate efficient manufacturing of the foam, particularly in terms of drying, it is desired that the foam is dimensionally stable also in the wet state. ln addition, it is also desired that the surface characteristics, such as surface gloss, smoothness, ink absorbency and hydrophobicity of the biobased foam can be tailored.
Summary of the invention lt is an object of the present invention to provide an improved solid cellulose foam, which foam is recyclable and made from renewable sources, and which eliminates or alleviates at least some of the disadvantages of the prior art materials. lt is a further object of the present invention to provide a solid cellulose foam that can be used in processes involving vacuum lifting and fixating equipment. lt is a further object of the present invention to provide a solid cellulose foam which enables tailormade surface characteristics depending on the use of the solid cellulose foam. lt is a further object of the present invention to provide a solid cellulose foam that can be produced by drying a wet foam without use of a mould to enable versatile production methods.
The above-mentioned objects, as well as other objects as will be realized by the skilled person in light of the present disclosure, are achieved by the various aspects of the present disclosure.
According to a first aspect, the present invention relates to a coated solid cellulose foam material having a density in the range of from 10 to 80 kg/ms; wherein the coated cellulose foam material comprises a solid cellulose foam having at least one coating on at least one outer surface, and wherein the at least one coating comprises at least one coating layer. lt has surprisingly been found that by applying a coating to at least one outer surface of the cellulose foam, the air permeability of the solid cellulose foam is decreased so that processes using vacuum lifting and fixating equipment can be used. This facilitates processing of the foam, particularly in terms of operations used when converting the foam for use in different packaging applications. The type of applied coating can further be selected so as to provide the solid cellulose foam with not only a decrease in air permeability, but also other desired properties such as surface smoothness, ink absorbency, hydrophobicity, resistance to scratching and surface gloss. The surface properties of the solid cellulose foam can be tailored depending on the end use of the foam by application of one or several coatings.
The cellulose foam preferably comprises in the range of from 71 to 95 wt% cellulose fibres, as calculated on the total weight of solid content in the foam, in the range of from 4 to 24 wt% of a water-soluble thickener, as calculated on the total weight of solid content in the foam, and at least two surfactants. A wet foam having such a composition will be free-standing and does not require a mould or any other forming means to retain its shape during drying.
According to a second aspect, the present invention relates to a method for coating a cellulose foam, the method comprising the following steps: a) providing a cellulose foam comprising at least one outer surface, and wherein the at least one outer surface is at least partially dry; b) providing at least one coating composition; c) applying at least one coating layer of the at least one coating composition to at least one outer surface of the cellulose foam so as to obtain a coated cellulose foam material; d) drying the coated cellulose foam material so as to obtain a coated solid cellulose foam material having a density in the range of from 10 to 80 kg/ms. lt has surprisingly been found that the coating layer can be applied to a cellulose foam that is at least partially dried. This enables a versatile processing method, where properties of the cellulose foam can be tailored by application of a certain coating. Since the coating can be applied to an at least partially dried foam, it is also possible to influence properties of the cellulose foam during processing. The coated solid cellulose foam material according to the first aspect may be produced by the method according to the second aspect.
According to a third aspect, the present invention relates to use of the coated solid cellulose foam material according to the first aspect in a packaging, as insulating material, or as a building material.
Detailed description The term "foam", as used herein, refers to a substance made by trapping air or gas bubbles inside a solid or liquid. Typically, the volume of gas is much larger than that of the liquid or solid, with thin films separating gas pockets. Three requirements must be met in order for foam to form. Mechanical work is needed to increase the surface area. This can occur by agitation, dispersing a large volume of gas into a liquid, or injecting a gas into a liquid. The second requirement is that a foam forming agent, typically an amphiphilic substance, a surfactant or surface active component, must be present to decrease surface tension. Finally, the foam must form more quickly than it breaks down.
The term "cellulose foam", as used herein, refers to a foam comprising cellulose, and other components such as thickeners, surfactants and additives. The main component of the cellulose foam is cellulose, such that cellulose constitutes at least 70 wt% of the dry content of the cellulose foam. Cellulose is in the form of fibres, and the foam can thus also be defined to be a fibrous foam or a cellulose fibre foam. The cellulose foam may be wet or solid.
The term "wet foam", or "wet cellulose foam", as used herein, refers to a wet foam comprising cellulose, and other components such as thickeners, surfactants and additives. Gas bubbles are present within the wet foam. The wet foam is freestanding and behaves as a viscoelastic solid. This means that the wet foam has both viscous and elastic properties. The wet foam will behave as a solid, and thus be freestanding, unless a large enough force is applied so that it starts to flow and instead behave as a viscous material. Depending on the magnitude and timescale of any applied shear stress, the wet foam can show a predominantly viscous or elastic behaviour.
The term "solid cellulose foam", or "dry cellulose foam", as used herein, refers to a dry porous cellulose material that has been formed from a wet cellulose foam, i.e. a foam formed material. During the drying process, a closed wet cellulose foam is transformed into an open solid cellulose foam. The network of cellulose fibres is prevented from collapsing during drying. The solid cellulose foam will as a result have a shape that to a large extent corresponds to that of the wet cellulose foam. The dry content of the solid cellulose foam is at least 95 wt% as calculated based on the total weight of the solid cellulose foam. The shape and density of the solid cellulose foam is retained also in a non-confined state. The solid cellulose foam has an open cell structure, allowing air to occupy the pores within the foam. The solid cellulose foam can also be described as a porous material or a low-density material.
The first aspect of the present invention relates to a coated solid cellulose foam material. The coated solid cellulose foam material is dry and may have a solid content in the range of from 95 to 100 wt%, preferably from 98 to 100 wt%, as calculated on the total weight of the coated solid cellulose foam material. The coated solid cellulose foam material has a density in the range of from 10 to 80 kg/ms, preferably from 10 to 60 kg/ms and more preferably from 20 to 50 kg/ms.
The coated solid cellulose foam material is prepared by applying at least one coating to at least one outer surface of a cellulose foam. The cellulose foam is preferably solid and may have a density in the range of from 10 to 80 kg/ms, preferably from 20 to 50 kg/ms and more preferably from 20 to 50 kg/ms. The applied coating layer is thin and thus has a negligent influence on the density of the coated solid cellulose foam material.
The cellulose foam preferably comprises cellulose fibres, in a range from 71 to 95 wt%, such as from 75 to 95 wt%, based on the total dry weight of the cellulose foam.
Cellulose fibres suitable for use in the present invention can originate from wood, such as softwood or hardwood, from leaves or from fibre crops (including cotton, flax and hemp). The cellulose fibres suitable for use in the present invention can also originate from regenerated cellulose such as rayon and Lyocell. The cellulose fibres suitable for use in the present invention may include lignin or hemicellulose or both, or the cellulose fibres may be free from lignin and hemicellulose. Preferably, the cellulose fibres originate from wood, more preferably the cellulose fibres are pulp fibres obtained by pulping processes which liberates the fibres from the wood matrix. Pulp fibres can be liberated by mechanical pulping, obtaining mechanical pulp such as thermos mechanical pulp (TMP) or chemo thermos mechanical pulp (CTl\/IP), or by chemical pulping such as Kraft pulp or pulps obtained by the sulphite process, soda process or organosolv pulping process. l\/lore preferably, the cellulose fibres are pulp fibres liberated by chemical pulping processes. The different characteristic of each cellulose fibre will affect the properties of the final cellulose foam. A cellulose fibre is significantly longer than it is wide. Celluiose fibres can have a mean width of 0.01 to 0.05 mm. The fibre length of softwood can be from 2.5 to 4.5 mm, while hardwood can have a fibre length from 0.7 to 1.6 mm, and Eucalyptus from 0.7 to 1.5 mm. However, the fibre length can vary considerably with different growing place etc. The cellulose fibres in the cellulose foam disclosed herein can have a length from 0.1 mm to 65 mm, or from 0.1 mm to 10 mm, or from 0.5 mm to 65 mm, or from 0.5 mm to 10 mm, or from 0.5 mm to 7mm. The fibre lengths may provide different mechanical characteristics to the foam. Due to the length of fibres, they can entangle with each other and impart fibre to fibre interbonds that bring strength to the foam. The aspect ratio, i.e. the ratio of the fibre length to the fibre width, of the cellulose fibres in the cellulose foam according to the present invention can be at least 10, at least 25, at least 50, at least 75, or at least 100, which provides for preservation and stabilization of the foam structure during the drying procedure, making it possible to dry the wet cellulose foam with retained shape. The aspect ratio can be up to 6500, or preferably up to 2000.
The cellulose fibres may be modified to provide different properties to the final cellulose foam. For example, phosphorylated fibres or periodate oxidized fibres could also be used when producing a cellulose foam according to the present invenfion.
Preferably, the cellulose fibres are selected from wood pulp, such as softwood Kraft bleached pulp, hardwood pulp, chemical-thermomechanical pulp, and from dissolving pulp, or a combination of one or more of these. l\/lore preferably the cellulose pulp fibres are from softwood pulp, chemical-thermomechanical pulp, or dissolving pulp. Most preferably the cellulose pulp fibres are from softwood pulp, such as softwood Kraft bleached pulp.
The cellulose foam preferably comprises cellulose fibres in a range of from 71 to 95 wt%, such as from 75 to 95 wt%, based on the total dry weight of the cellulose foam, a water-soluble thickener in a range of from 4 to 24 wt%, such as from 5 to 20 wt%, based on the total dry weight of the cellulose foam, and at least two surfactants.
The water-soluble thickener may have a molecular weight of from 80 000-250 000 g/mol, or from 83 000-197 000 g/mol. Exemplary water-soluble thickeners are selected from carboxy methyl cellulose (GMC), methyl cellulose (MC), hydroxyethyl cellulose (HEC), ethyl hydroxyethyl cellulose (EHEC), methyl hydroxypropyl cellulose (MHPC), starch, xanthan, guar gum, and xyloglucan, or mixtures thereof. The fact that the thickener is water-soluble facilitates recycling of the cellulose foam.
The water-soluble thickener may improve the fibre-fibre bonding strength, primarily through hydrogen bonding, in the cellulose foam, Therefore, the amount of water- soluble thickener will influence the mechanical performance of the cellulose foam, and especially the bulk of the material. A higher content of water-soluble thickener provides for a stiffer material. Thus, the water-soluble thickener enables tailoring of the mechanical properties of the cellulose foam.
The cellulose foam may also comprise a mixture of at least two surfactants. One of the at least two surfactants is preferably a fast-acting surfactant, a suitable surfactant for this purpose is an anionic surfactant, preferably a low-molecular weight anionic surfactant. The anionic surfactant may have an apparent pKa of from 3.2 to 3.8, preferably from 3.4 to 3.6, or an apparent pKa of 3.5 in a solution having a pH of from 7 to 9, preferably a pH of 8. The low-molecular weight anionic surfactant may be selected from sodium dodecyl sulphate (SDS); potassium dodecyl sulphate, sodium laureth sulphate (SLES); sodium dodecylbenzenesulphonate; sodium cocoyl sarcosinate; sodium lauroyl sarcosinate. The low-molecular weight anionic surfactant is preferably selected from sodium dodecyl sulphate (SDS); sodium p-n-dodecylbenzenesulphonate; sodium cocoyl sarcosinate; and sodium lauroyl sarcosinate. l\/lore preferably the low-molecular weight anionic surfactant is sodium cocoyl sarcosinate. The anionic surfactant may be biodegradable.
The other one of the at least two surfactants is preferably a co-surfactant. The co- surfactant may be selected from the group comprising surfactants having an apparent pKa of at least 8, or at least 9, in a surfactant solution having pH of from 7 to 9, preferably having a pH of 8; and amphoteric betaines. The co-surfactant may have maximum apparent pKa of 10. The co-surfactant preferably has a long carbon chain, more preferably a carbon chain with 14 carbon atoms (C14). The co- surfactant may be selected from high pKa fatty acids, such as from plant derived feedstock, e.g. tetradecanoic acid (myristic acid), sodium oleate, lauric acid, palmitic acid, and stearic acid; glucose based co-surfactants with an aliphatic carbon tail, such as alkyl glycosides, alkylpolyglucosides, alkyl thio-glycosides, and alkyl maltosides; amphoteric betaines, such as cocamidopropyl betaine (CAPB), and sodium cocoiminodipropionate (CADP); polyethylene glycol sorbitan monolaurate, i.e. tween® (e.g. tween® 20, tween® 80 and tween® 85); and polyoxyethylene lauryl ethers, such as polyethylene glycol dodecyl ether, pentaethylene glycol monododecyl ether and octaethylene glycol monododecyl ether.
Thus, the at least two surfactants used in the cellulose foam preferably comprise a mixture of an anionic surfactant and a co-surfactant. The molar ratio between anionic surfactant to co-surfactant may be from 0.2:1-3:1, preferably from 0.5:1 to 2:1. The total amount of the at least two surfactants together in the cellulose foam may be 0.6-5 wt%, or 0.8-2.0 wt%, as calculated on the total weight of the cellulose foam.
The cellulose foam can be re-dispersed in water and as a result be recyclable in regular paper recycling streams.
The cellulose foam may be prepared using a method comprising the following steps: - disintegrating cellulose fibres in water to obtain a slurry of cellulose fibres; - adding a water-soluble thickener to the slurry to obtain a mixture of thickener and cellulose fibres in water; - adding at least two surfactants to the mixture to obtain a fibre suspension; and - aerating the fibre suspension to obtain a wet foam, wherein the wet foam comprises 10-38 wt% cellulose fibres, 0.5-10 wt% of the water-soluble thickener, and 0.1-2 wt% surfactants, as calculated on the total weight of the wet foam, and wherein the foam has a density of from 140-500 kg/ms and a yield stress of from 40 to 400 Pa; - drying the wet foam to obtain a solid cellulose foam.
The drying step can be omitted if a solid cellulose foam is not desired. The drying step can also be carried out only until a partially dried cellulose foam is obtained.
Addition of a water-soluble thickener increase the viscosity of the slurry and enables incorporation of enough air to generate a densely packed foam during aeration. Since the cellulose fibres are mixed in high concentrations a drainage step is not needed, which enables the use of a water-soluble bio-based thickener in high concentrations.
Addition of a fast-acting surfactant will contribute to the formation of a cellulose foam with a high density and a high viscosity as it will quickly settle at the air-water interphase during aeration. This enables a free-standing wet cellulose foam. Addition of a co-surfactant along with the fast-acting surfactant will further improve the properties of the cellulose foam since it will facilitate the action of the fast-acting surfactant. A co-surfactant having a suitable pKa and a long carbon chain further contributes to a stable fibre suspension and a stable wet cellulose foam.
Upon aeration the composition comprising cellulose fibres, thickener and at least tvvo surfactants will form a highly stable wet fibre foam. The aeration may be performed by mechanical agitation, and a substantial amount of air is incorporated into the material. The formation of a foam will be promoted by the surfactants. By adjusting the stability of the wet foam with the use of thickeners and surfactant combinations, a free-standing cellulose foam can be made without the use of a cross-linker or fibrillated cellulose. A good stability of the foam prevents ripening, i.e. change in bubble size, and drainage. The obtained wet foam is free-standing and does not require a mould or a forming fabric to retain its shape upon drying. The wet foam can thus be formed into a free-standing foam that is stable enough to be dried in the absence of a supporting mould without collapsing. As a result, objects can be formed and dried without the use of a mould.
Because of the high solid content, the wet foam does not need to be dewatered before it is dried. The foam may be dried by evaporation at room temperature or at an elevated temperature, such as a temperature of from 40 -140 °C. The dry cellulose foam may have a density of from 10 to 80 kg/ms, or from 10 to 60 kg/ms, or from 20 to 50 kg/ms. 11 The solid cellulose foam may have any shape, such as a block, a cube, a cylinder or any irregular shape. Regardless of the shape, the solid cellulose foam will have at least one outer surface. The term "outer surface" as used herein refers to the outermost surface of the solid cellulose foam. lt is not intended to mean the outermost surface of any final foam product. ln the present invention, the outer surface of the solid cellulose foam is coated with at least one coating layer. lt may further be covered with other layers, such as an additional layer of a cellulose foam. ln one embodiment, the solid cellulose foam is provided in the form of a plank having a thickness in the range of from 1 to 20 cm, preferably from 1 to 10 cm, more preferably from 4 to 6 cm. The length and width dimensions of the plank are typically in the range of from 100 to 300 cm. The planks may be cut into smaller pieces but preferably having the same thickness. ln embodiments where the solid cellulose foam is provided in the form of a plank, outer surfaces are thus present on the top surface, the bottom surface and the side surfaces of the plank.
The solid cellulose foam may on at least one outer surface have a densified layer. ln embodiments where the cellulose foam is provided in the form of a plank, the cellulose foam has densified layers on at least the top surface and bottom surface, and optionally on the side surfaces.
The densified layer comprises cellulose fibres that are packed more tightly and partly oriented differently compared to the bulk leading to a higher number of fibre- fibre bonds. The densified layer is formed on the outer surface of the wet foam during drying of the wet foam and remain on the outer surface of the solid cellulose foam when dried. The densified layers have improved mechanical stability and strength as compared to the core of the solid cellulose foam. The core of the solid cellulose foam comprises a homogenous open-cell fibre network. The core is highly porous, and even though the densified layer has a denser structure than the core, it is still porous.
The densified layer thus provides the solid cellulose foam with increased stability and mechanical strength. ln embodiments where the solid cellulose foam is provided in the form of a plank, it is therefore preferable that during cutting of the foam planks, cutting is carried out such that the thickness of the planks remains the same 12 also after cutting, thus ensuring that the densified layers are still present on the top surface and bottom surface.
According to the first aspect of the present invention, the solid cellulose foam is provided with at least one coating on at least one outer surface. The solid cellulose foam may be provided with a coating on one outer surface, or on several outer surfaces or on all outer surfaces. ln embodiments where the solid cellulose foam is provided with a coating on more than one outer surface, the composition of the coating on the coated outer surfaces may be identical or different. For example, the solid cellulose foam may be provided with a first type of coating on a first outer surface and a second type of coating on a second outer surface. lt is also within the scope of the present invention to provide more than one coating on the same outer surface, e.g. that a first part of the outer surface may be covered with a first coating and a second part of the outer surface may be covered with a second coating. ln embodiments where the solid cellulose foam is provided in the form of a plank, it may be provided with a coating on the top surface, on the bottom surface and/or on any of the side surfaces.
The coating is preferably provided on an outer surface of the solid cellulose foam comprising a densified layer, since the densified layer is smoother and has a less open structure than an outer surface not comprising a densified layer. ln embodiments where not all outer surfaces of the solid cellulose foam comprise densified layers, the coating may be provided both on surfaces comprising the densified layers and on outer surfaces that do not comprise a densified layer.
An adhesive layer may be provided on the at least one outer surface of the cellulose foam, or on the densified layer if present. ln such embodiments, the coating is provided on the adhesive layer. Preferably, the coating is provided directly onto the solid cellulose foam, i.e. without the use of an adhesive layer.
The coating comprises at least one coating layer, such as at least two coating layers or at least three coating layers. ln embodiments where the coating comprises at least two coating layers, the composition of the at least two coating layers may be identical or different. 13 ln embodiments where the solid cellulose substrate is provided with a coating on more than one outer surface, each coating may comprise at least one coating layer, such as at least two coating layers or at least three coating layers.
The term "composition" as used herein refers to the composition of a coating in terms of its components. Compositions may differ from each other in terms of concentration of the components, or in terms of the components present in the composition, or a combination of both.
The application of a coating on the outer surface of the solid cellulose foam will decrease the air permeability of the solid cellulose foam since pores on the outer surface are closed by the coating. To sufficiently close all pores on the surface, it is important that the coating is sufficiently thick, and the surface of the foam must be relatively flat. ln some embodiments, the at least one coating has a basis weight in the range of from 2 to 500 g/m2, such as from 2 to 300 g/m2, or from 2 to 250 g/m2, or from 10 to 200 g/m2, or from 10 to 150 g/m2, or from 50 to 150 g/m2, or from 50 to 300 g/m2. By decreasing the air permeability of the cellulose foam by application of at least one coating on at least one outer surface, use of the resulting coated solid cellulose foam material in automated processes involving vacuum is greatly facilitated. The coated solid cellulose foam may for example be used in converting and packaging processes involving steps requiring vacuum lifting and fixation.
Since the coating is thin, it has a negligible effect on the density of the coated solid cellulose material. Thus, the density of the coated solid cellulose material is also within the range of from 10 to 80 kg/ms, or from 10 to 60 kg/ms, or from 20 to 50 kg/ms.
The coating is provided by application of at least one layer of at least one coating composition to the at least one outer surface of the cellulose foam. The coating composition is preferably a liquid, such as a water-based suspension or dispersion.
The coating may comprise at least one particulate material and at least one film- forming material. A coating comprising at least one particulate material and at least one film-forming material will increase the coverage of the coating on the outer surface of the cellulose foam and thus decrease the risk of formation of pin holes, which if present would negatively influence the air permeability of the cellulose foam. 14 ln addition, the smoothness and gloss of the coated solid cellulose foam material may be improved. Further, the ink absorbency may be improved by providing a coating, thus allowing for improved printability in terms of a higher definition printing, since ink will not bleed into the coated solid cellulose foam material.
The coating composition may comprise at least one particulate material and at least one film-forming material. For example, the coating composition may comprise a particulate material, a film-forming material, optionally at least one additive, and water.
The particulate material may be selected from at least one of microfibrillated cellulose (MFC), cellulose fibres, mineral particles such as clay or calcium carbonate.
The film-forming material may be selected from at least one of carboxymethyl cellulose (CMC), cellulose ethers, starch, polyvinyl alcohol or synthetic latexes, such as acrylic or styrene-butadiene latexes.
For example, the coating may comprise CMC, calcium carbonate and glycerol (acting as a plasticizer). The corresponding coating composition comprises CMC, calcium carbonate, glycerol and water. ln one embodiment, the coating comprises MFC. The corresponding coating composition comprises MFC and water. Microfibrillated cellulose (MFC) shall in the context of the patent application mean a cellulose particle, fiber or fibril having a width or diameter of from 20 nm to 1000 nm.
Various methods exist to make MFC, such as single or multiple pass refining, pre- hydrolysis followed by refining or high shear disintegration or liberation of fibrils. One or several pre-treatment steps is usually required in order to make MFC manufacturing both energy efficient and sustainable. The cellulose fibers of the pulp used when producing MFC may thus be native or pre-treated enzymatically or chemically, for example to reduce the quantity of hemicellulose or lignin. The cellulose fibers may be chemically modified before fibrillation, wherein the cellulose molecules contain functional groups other (or more) than found in the original cellulose. Such groups include, among others, carboxymethyl (CM), aldehyde and/or carboxyl groups (cellulose obtained by N-oxyl mediated oxidation, for example "TEMPO"), or quaternary ammonium (cationic cellulose). After being modified or oxidized in one of the above-described methods, it is easier to disintegrate the fibers into MFC.
MFC can be produced from wood cellulose fibers, both from hardwood or softwood fibers. lt can also be made from microbial sources, agricultural fibers such as wheat straw pulp, bamboo, bagasse, or other non-wood fiber sources. lt can be made from pulp, including pulp from virgin fiber, e.g. mechanical, chemical and/or thermomechanical pulps. lt can also be made from broke or recycled paper.
A coating comprising MFC will have excellent strength properties as well as a good coverage of pores in the solid cellulose foam, thus providing the coated solid cellulose foam with an improved strength as well as a decreased air permeability. ln addition, a coating based on MFC is of advantage when it comes to recycling of the coated cellulose foam material. MFC may in some embodiments act both as a particulate material and a film-forming material. For example, the coating may consist entirely of MFC. ln another example, the coating comprises MFC, CMC and a plasticizer, such as glycerol. The corresponding coating compositions used for providing the coatings would comprise MFC and water; and MFC, CMC, plasticizer, and water respectively. ln one embodiment, the coating comprises cellulose fibres. The corresponding coating composition comprises cellulose fibres. The cellulose fibres may be selected from wood pulp; regenerated cellulose fibres; and plant fibres, such as fibres from bamboo, cotton, hemp, flax, and jute. Preferably, the cellulose fibres are selected from wood pulp, such as softwood pulp, hardwood pulp, chemical- thermomechanical pulp, and from dissolving pulp, or a combination of one or more of these.
A coating comprising cellulose fibres may have a good coverage of pores in the solid cellulose foam. For example, the coating may comprise cellulose fibres and various additives typically used in paper manufacturing. The corresponding coating composition used for providing the coating would comprise cellulose fibres, additives and water. 16 The coating may optionally comprise at least one additive, such as dispersants, de- foamers, UV-absorbers, plasticizers, wet-resistance additives and strength additives. Addition of at least one additive to the coating will provide the coating with improved properties. ln one embodiment, the coating comprises at least one hydrophobic agent. The corresponding coating composition comprises at least one hydrophobic agent. The hydrophobic agent may be selected from at least one of a wax, such as bee's wax or carnauba, alkyl ketene dimer (AKD) or alkyl succinic anhydride (ASA). ln some embodiments, the coating may comprise a hydrophobic agent as well as a particulate material and a film-forming material. ln such embodiments, the hydrophobic agent may be part of the same coating layer as the particulate material and the film-forming material, or it may form a different coating layer.
The coating composition comprising at least one hydrophobic agent may be a water- based emulsion, or it may be a solution comprising the hydrophobic agent and at least one solvent, such as an alcohol.
The at least one hydrophobic agent provides hydrophobic properties to the coating. This is of particular importance in applications where improved water resistance is required, such as when using the coated solid cellulose foam material in thermal packaging solutions where condensation may pose a problem. ln embodiments where the coating comprises at least two coating layers, the composition of the at least two coating layers may be identical or different. For example, two or more coating layers of the same coating composition may be applied to the cellulose foam, such as two layers of a coating composition comprising MFC. ln another example, two coating layers of different coating compositions may be applied to the cellulose foam, such as a first coating layer of a coating composition comprising l\/IFC and a second coating layer of a coating composition comprising a hydrophobic agent. lf a coated solid cellulose material having improved water resistance is required, it is advantageous to have an outermost coating layer that comprises a hydrophobic agent. 17 ln embodiments where the coating comprises at least two coating layers, the first coating layer is applied to the outer surface of the cellulose foam, and the second coating layer is applied on top of the first coating layer, and so on. ln embodiments where at least two outer surfaces of the solid cellulose foam are provided with a coating, the at least two coatings may be identical or different. For example, one or more coating layers of a coating composition comprising l\/IFC may be applied on all outer surfaces of a solid cellulose foam. ln another example, one or more coating layers of a coating composition comprising l\/IFC may be applied on a first outer surface of a cellulose foam, and a coating composition comprising a hydrophobic agent may be applied on a second outer surface of said cellulose foam. ln some embodiments an additional layer of material, such as a fibrous substrate or a second cellulose foam, is applied on top of the at least one coating, so that the coating is sandwiched between the cellulose foam and the additional layer of material. At least one coating may be applied also on at least one outer surface of the additional layer of material. ln some embodiments, the solid cellulose foam may be prepared by a two-step deposition. ln a first deposition, a wet foam is deposited as discrete units on a surface and at least partially dried. During drying, a densified layer is formed on the outer surface of the discrete units. ln a second deposition a wet foam, preferably having the same composition as the wet foam in the first deposition, is deposited so that it fills the spaces surrounding the discrete units of the first deposition. After drying, a solid cellulose foam comprising discrete units of foam embedded in a foam matrix is obtained. The densified layer on the outer surface of the discrete units provides mechanical support during drying of the foam in the second deposition and the entire cellulose foam by helping to keep the shape of the discrete units. A coating may be applied to at least one outer surface of the solid cellulose foam comprising discrete units of foam embedded in a foam matrix. A coating may also be applied to the outer surface of the discrete units, prior to depositing the second deposition. The coating is applied to the outer surface of the discrete units when the discrete units have been at least partially dried, so that the outer surface of the discrete units comprises a densified layer when the coating is applied. ln one example, a coating composition comprising MFC is applied to an outer surface of the at least partially dried discrete units, and a coating composition comprising a 18 hydrophobic agent is applied to an outer surface of the solid cellulose foam comprising discrete units embedded in a foam matrix, i.e. after the second deposition.
By selection of what type of coating(s) to apply on a cellulose foam, the properties of the obtained coated solid cellulose foam material can be carefully tailored.
According to a second aspect, the present invention relates to a method for coating a cellulose foam. Step a) of the method according to the second aspect involves providing a cellulose foam comprising at least one outer surface. The cellulose foam provided in step a) is at least partially dry. ln the context of the present invention, at least partially dry means that at least the outer surface of the cellulose foam is dry, so that a coating can be applied on it. ln a preferred embodiment, the provided cellulose foam is dry and may have a solid content in the range of from 95 to 100 wt%, preferably from 98 to 100 wt%, as calculated on the total weight of the cellulose foam. Thus, preferably a solid cellulose foam is provided in step a). The density of the solid cellulose foam may be in the range of from 10 to 80 kg/ms, such as from 10 to 60 kg/ms, or from 20 to 50 kg/ms. The cellulose foam may be further defined as set out above with reference to the first aspect.
Step b) of the method according to the second aspect involves providing at least one coating composition. The coating composition is preferably a liquid, such as an aqueous dispersion, suspension or emulsion. Other suitable solvents than water may also be used. The coating composition may be further defined as set out above with reference to the first aspect.
Step c) of the method according to the second aspect involves applying at least one coating layer of the at least one coating composition to at least one outer surface of the cellulose foam so as to obtain a coated cellulose foam material. The coating composition may be applied using any suitable method used for coating such as roller coating, blade/knife coating, brushing, flexo roller, and spray coating. ln embodiments where more than one coating layer is applied, the coating compositions of the respective coating layers may be applied using the same coating method, or different ones. Different combinations of coating layers may be applied depending on the desired properties of the coated cellulose foam material, as further set out above with reference to the first aspect. 19 Step d) of the method according to the second aspect involves drying the coated cellulose foam material so as to obtain a coated solid cellulose foam material having a density in the range of from 10 to 80 kg/ms, such as from 10 to 60 kg/ms, or from 20 to 50 kg/ms. The coated cellulose foam material may be dried by evaporation at room temperature or at an elevated temperature, such as a temperature of from 40 to 140°C. Any suitable drying equipment, such as anoven, or infrared heating, may be used. ln embodiments where at least two coating layers are applied, the first coating layer may be dried before application of the second coating layer. lf a third coating layer is to be applied, the second coating layer may be dried before application of the third layer, and so on. ln an alternative embodiment, the first coating layer is not dried before application of the second coating layer.
Examples Example 1 - preparation of foam A uniform wet paste comprising 12 wt% cellulose pulp (softwood bleached Kraft pulp) and a 1.2 wt% thickener (GMC) in water was prepared. The wet paste was aerated with a surfactant mixture (myristic acid and sodium cocoyl sarcosinate) until a desired wet foam density was obtained. A cylindrical mould with the dimension of 2.5 cm in height and 6.6 cm in diameter were used to deposit discrete units of the foam on a flat surface. The moulds were used only for depositing the wet foam in the desired shape and dimension and were removed before the foam was dried. The shaped foam was dried in an ordinary convection oven at 120°C until completely dry. The dry cellulose foam had a density of 30 kg/ms.
Example 2 A cylindrical dry cellulose foam prepared as described for example 1 was coated with an aqueous solution comprising microfibrillated cellulose (2 wt%). The coating was applied on all sides of the cellulose foam using a brush and ensuring that the applied coating layer was thick enough to cover the surface of the foam. The MFC- coating was applied on the densified layers on the outer surfaces of the foam.
The air permeability of the cellulose foam was reduced by the MFC-coating. ln addition, the smoothness of the surface of the foam was improved by the coating.
Further, the strength of the densified layer was improved by the coating. This was evident as the properties during impact testing was better than for a foam without an MFC-coating. The degradation over time was also less for the foam with an MFC- coating compared to a foam with no coating. Comparisons are made with a foam according to example 1.
Example 3 A cylindrical dry cellulose foam prepared as described in example 1 was coated with an aqueous coating comprising CaCOs and CMC. The coating solution was prepared by dispersing calcium carbonate in an 8% (w/w) aqueous CMC solution such that the final solid content was 40% (w/w). The coating was applied on all sides of the foam using a brush and ensuring that the applied coating layer was thick enough to cover the surface of the foam. The coated foams were dried in an oven at 120°C until completely dry The air permeability of the cellulose foam was reduced by the coating, and it was evident that the coating blocked pores on the surface, and the air permeability was decreased. lt was also evident that the surface of the foam became smoother after application of the coating.
Example 4 The same as example 3, but with the addition of glycerol (8 w/w) to the CMC coating solution. The coating was improved by addition of glycerol, further reducing the air permeability of the cellulose foam after application of the coating as compared to the coating in example 3. ln view of the above detailed description of the present invention, other modifications and variations will become apparent to those skilled in the art. However, it should be apparent that such other modifications and variations may be effected without departing from the spirit and scope of the invention.
Claims (1)
1.Claims A coated solid cellulose foam material having a density in the range of from 10 to 80 kg/ms; wherein the coated cellulose foam material comprises a solid cellulose foam having at least one coating on at least one outer surface, and wherein the at least one coating comprises at least one coating layer. The coated solid cellulose foam material according to claim 1, wherein the cellulose foam comprises cellulose fibres in a range of from 71 to 95 wt% based on the total dry weight of the solid cellulose foam. The coated solid cellulose foam material according to any one of claims 1 or 2, wherein the solid cellulose foam comprises: cellulose fibres in a range of from 71 to 95 wt% based on the total dry weight of the solid cellulose foam, a water-soluble thickener in a range of from 4 to 24 wt% based on the total dry weight of the solid cellulose foam, and at least two surfactants. The coated solid cellulose foam material according to any one of the preceding claims, wherein at least one outer surface of the solid cellulose foam comprises a densified layer. The coated solid cellulose foam material according to claim 4, wherein the at least one coating is provided on the densified layer. The coated solid cellulose foam material according to any one of the preceding claims, wherein the at least one coating comprises at least two coating layers, and wherein the composition of the at least two coating layers may be identical or different. The coated solid cellulose foam material according to any one of the preceding claims, wherein the coating comprises at least one particulate material and at least one film-forming material.The coated solid cellulose foam material according to any one of the preceding claims, wherein the coating comprises microfibrillated cellulose (MFC). The coated solid cellulose foam material according to any one of the preceding claims, wherein the coating comprises at least one hydrophobic agent. The coated solid cellulose foam substrate according to any one of the preceding claims, wherein the coating has a basis weight in the range of from 2 to 300 g/m A method for coating a cellulose foam, the method comprising the following steps: a) providing a cellulose foam comprising at least one outer surface, and wherein the at least one outer surface is at least partially dry; b) providing at least one coating composition; c) applying at least one coating layer of the at least one coating composition to at least one outer surface of the cellulose foam so as to obtain a coated cellulose foam material; d) drying the coated cellulose foam material so as to obtain a coated solid cellulose foam material having a density in the range of from 10 to 80 kg/ms. The method according to claim 11, wherein the cellulose foam comprises cellulose fibres in a range of from 71 to 95 wt% based on the total dry weight of the cellulose foam. The method according to any one of claims 11 or 12, wherein the cellulose foam comprises: cellulose fibres in a range of from 71 to 95 wt% based on the total dry weight of the cellulose foam, a water-soluble thickener in a range of from 4 to 24 wt% based on the total dry weight of the cellulose foam, and at least two surfactants. The method according to any one of claims 11-13, wherein the at least one coating composition is provided in the form of a liquid.The method according to any one of claims 11-14, wherein at least two coating layers are applied, and wherein the coating composition in the at least two coating layers may be identical or different. The method according to any one of claims 11-15, wherein the provided cellulose foam is a solid cellulose foam, having a density in the range of from 10 to 80 kg/ms. The method according to any one of claims 11-16, wherein the at least one coating composition comprises at least one particulate material and at least one film-forming material. The method according to any one of claims 11-17, wherein the at least one coating composition comprises MFC. The method according to any one of claims 11-18, wherein the at least one coating composition comprises at least one hydrophobic agent. Use of the coated solid cellulose foam material according to any one of claims 1-10 as packaging material, as insulating material, or as a building material.
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE2230310A SE2230310A1 (en) | 2022-09-23 | 2022-09-23 | A coated solid cellulose foam material |
CN202280085695.0A CN118434798A (en) | 2021-12-22 | 2022-12-22 | Preparation of foam comprising discrete units of foam embedded in a foam matrix |
JP2024538097A JP2024545323A (en) | 2021-12-22 | 2022-12-22 | Preparation of foams containing individual units of foam embedded in a foam matrix |
PCT/IB2022/062666 WO2023119215A1 (en) | 2021-12-22 | 2022-12-22 | Preparation of a foam comprising discrete units of foam embedded in a foam matrix |
EP22910342.9A EP4453073A1 (en) | 2021-12-22 | 2022-12-22 | Preparation of a foam comprising discrete units of foam embedded in a foam matrix |
MX2024007644A MX2024007644A (en) | 2021-12-22 | 2022-12-22 | Preparation of a foam comprising discrete units of foam embedded in a foam matrix. |
PCT/IB2023/059382 WO2024062436A1 (en) | 2022-09-23 | 2023-09-22 | A coated solid cellulose foam material |
Applications Claiming Priority (1)
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SE2230310A SE2230310A1 (en) | 2022-09-23 | 2022-09-23 | A coated solid cellulose foam material |
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SE2230310A1 true SE2230310A1 (en) | 2024-03-24 |
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SE2230310A SE2230310A1 (en) | 2021-12-22 | 2022-09-23 | A coated solid cellulose foam material |
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CN (1) | CN118434798A (en) |
SE (1) | SE2230310A1 (en) |
WO (1) | WO2024062436A1 (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050255284A1 (en) * | 2004-05-14 | 2005-11-17 | Pritchett Joseph E | Method of applying a heat reflective coating to a substrate sheet |
US20160289453A1 (en) * | 2013-11-05 | 2016-10-06 | Fpinnovations | Method of producing ultra-low density fiber composite materials |
US20170120556A1 (en) * | 2014-05-28 | 2017-05-04 | Tetra Laval Holdings & Finance S.A. | Packaging material and packaging container |
US20200039713A1 (en) * | 2016-10-14 | 2020-02-06 | Tetra Laval Holdings & Finance S.A. | Method of manufacturing of a foam-formed cellulosic fibre material, sheet and laminated packaging material |
-
2022
- 2022-09-23 SE SE2230310A patent/SE2230310A1/en unknown
- 2022-12-22 CN CN202280085695.0A patent/CN118434798A/en active Pending
-
2023
- 2023-09-22 WO PCT/IB2023/059382 patent/WO2024062436A1/en unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050255284A1 (en) * | 2004-05-14 | 2005-11-17 | Pritchett Joseph E | Method of applying a heat reflective coating to a substrate sheet |
US20160289453A1 (en) * | 2013-11-05 | 2016-10-06 | Fpinnovations | Method of producing ultra-low density fiber composite materials |
US20170120556A1 (en) * | 2014-05-28 | 2017-05-04 | Tetra Laval Holdings & Finance S.A. | Packaging material and packaging container |
US20200039713A1 (en) * | 2016-10-14 | 2020-02-06 | Tetra Laval Holdings & Finance S.A. | Method of manufacturing of a foam-formed cellulosic fibre material, sheet and laminated packaging material |
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WO2024062436A1 (en) | 2024-03-28 |
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