EP2021170A1 - Lasttragstruktur - Google Patents
LasttragstrukturInfo
- Publication number
- EP2021170A1 EP2021170A1 EP07776473A EP07776473A EP2021170A1 EP 2021170 A1 EP2021170 A1 EP 2021170A1 EP 07776473 A EP07776473 A EP 07776473A EP 07776473 A EP07776473 A EP 07776473A EP 2021170 A1 EP2021170 A1 EP 2021170A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- load
- bearing platform
- platform according
- expandable
- polymer matrix
- 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.)
- Withdrawn
Links
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- 239000000178 monomer Substances 0.000 claims abstract description 55
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 46
- 229920000098 polyolefin Polymers 0.000 claims abstract description 41
- 239000011159 matrix material Substances 0.000 claims abstract description 37
- 238000011065 in-situ storage Methods 0.000 claims abstract description 15
- 239000002245 particle Substances 0.000 claims description 43
- -1 polyethylene Polymers 0.000 claims description 32
- 229920005989 resin Polymers 0.000 claims description 27
- 239000011347 resin Substances 0.000 claims description 27
- 229920001577 copolymer Polymers 0.000 claims description 25
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 22
- 239000004604 Blowing Agent Substances 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 16
- 229920001971 elastomer Polymers 0.000 claims description 15
- 239000005060 rubber Substances 0.000 claims description 15
- 239000004014 plasticizer Substances 0.000 claims description 13
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 11
- 239000005977 Ethylene Substances 0.000 claims description 11
- 239000004698 Polyethylene Substances 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- 229920000573 polyethylene Polymers 0.000 claims description 10
- 238000006116 polymerization reaction Methods 0.000 claims description 8
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 6
- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 claims description 5
- GDEQPEBFOWYWSA-UHFFFAOYSA-N 1,2-dimethyl-3-propan-2-ylbenzene Chemical group CC(C)C1=CC=CC(C)=C1C GDEQPEBFOWYWSA-UHFFFAOYSA-N 0.000 claims description 4
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 claims description 4
- 239000004743 Polypropylene Substances 0.000 claims description 4
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- YMOONIIMQBGTDU-VOTSOKGWSA-N [(e)-2-bromoethenyl]benzene Chemical compound Br\C=C\C1=CC=CC=C1 YMOONIIMQBGTDU-VOTSOKGWSA-N 0.000 claims description 4
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- 229920006248 expandable polystyrene Polymers 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 4
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims description 4
- 125000005907 alkyl ester group Chemical group 0.000 claims description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 2
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- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- QYMGIIIPAFAFRX-UHFFFAOYSA-N butyl prop-2-enoate;ethene Chemical compound C=C.CCCCOC(=O)C=C QYMGIIIPAFAFRX-UHFFFAOYSA-N 0.000 claims description 2
- 150000001993 dienes Chemical class 0.000 claims description 2
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- 229920001903 high density polyethylene Polymers 0.000 claims description 2
- 239000004700 high-density polyethylene Substances 0.000 claims description 2
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- 239000004701 medium-density polyethylene Substances 0.000 claims description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 2
- 150000002825 nitriles Chemical class 0.000 claims description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 2
- 229920006380 polyphenylene oxide Polymers 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 13
- 239000011324 bead Substances 0.000 description 13
- 239000002023 wood Substances 0.000 description 11
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 9
- 125000004122 cyclic group Chemical group 0.000 description 8
- 239000003999 initiator Substances 0.000 description 8
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000003431 cross linking reagent Substances 0.000 description 7
- 229920001519 homopolymer Polymers 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 6
- 239000012736 aqueous medium Substances 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 5
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 5
- 210000002105 tongue Anatomy 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 4
- 229940087305 limonene Drugs 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- CRSOQBOWXPBRES-UHFFFAOYSA-N neopentane Chemical compound CC(C)(C)C CRSOQBOWXPBRES-UHFFFAOYSA-N 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 230000000379 polymerizing effect Effects 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 3
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 3
- 235000014036 Castanea Nutrition 0.000 description 3
- 241001070941 Castanea Species 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 241000238631 Hexapoda Species 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 229920000459 Nitrile rubber Polymers 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000001506 calcium phosphate Substances 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 235000001510 limonene Nutrition 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 3
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical compound CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- 241000243771 Bursaphelenchus xylophilus Species 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 2
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 2
- 229910000389 calcium phosphate Inorganic materials 0.000 description 2
- 235000011010 calcium phosphates Nutrition 0.000 description 2
- 210000003850 cellular structure Anatomy 0.000 description 2
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 2
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- 229940087091 dichlorotetrafluoroethane Drugs 0.000 description 2
- XZTWHWHGBBCSMX-UHFFFAOYSA-J dimagnesium;phosphonato phosphate Chemical compound [Mg+2].[Mg+2].[O-]P([O-])(=O)OP([O-])([O-])=O XZTWHWHGBBCSMX-UHFFFAOYSA-J 0.000 description 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 2
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- 150000002430 hydrocarbons Chemical class 0.000 description 2
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- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
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- 238000013019 agitation Methods 0.000 description 1
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- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
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- 238000005259 measurement Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
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- 239000013518 molded foam Substances 0.000 description 1
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- 229930003658 monoterpene Natural products 0.000 description 1
- 235000002577 monoterpenes Nutrition 0.000 description 1
- HZHRYYYIOGLPCB-UHFFFAOYSA-N n,n-bis(hydroxymethyl)prop-2-enamide Chemical compound OCN(CO)C(=O)C=C HZHRYYYIOGLPCB-UHFFFAOYSA-N 0.000 description 1
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- XZXKNOKYHJCUMT-UHFFFAOYSA-N n-ethoxy-2-(hydroxymethyl)prop-2-enamide Chemical compound CCONC(=O)C(=C)CO XZXKNOKYHJCUMT-UHFFFAOYSA-N 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
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- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
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- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- WMXCDAVJEZZYLT-UHFFFAOYSA-N tert-butylthiol Chemical compound CC(C)(C)S WMXCDAVJEZZYLT-UHFFFAOYSA-N 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- B22C1/20—Compositions of refractory mould or core materials; Grain structures thereof; Chemical or physical features in the formation or manufacture of moulds characterised by the use of binding agents; Mixtures of binding agents of organic agents
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
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- B65D2519/00004—Details relating to pallets
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- B65D2519/00288—Overall construction of the load supporting surface made of one piece
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- 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
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- B65D2519/00258—Overall construction
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- B65D2519/00328—Overall construction of the base surface shape of the contact surface of the base
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- 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
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- B65D2519/00004—Details relating to pallets
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Definitions
- the present invention is directed to novel load- bearing structures, such as pallets, generally used for stacking articles on for storage and/or shipping.
- a shipping pallet is a well known load-bearing, moveable platform whereon articles are placed for storage and/or shipment.
- the pallet usually is loaded with a multiplicity of items, such as cartons or boxes.
- the loaded pallet is movable, usually with the aid of either a pallet truck or a forklift.
- pallets are made from wood.
- the weight of the wood pallet is in the range of from forty to seventy pounds. Therefore, the weight of cargo shipped on the wood pallet is reduced by from forty to seventy pounds to provide for the weight of the wood pallet. This severely limits the amount of goods that can be shipped, especially by air.
- U.S. Patent No. 6,786,992 discloses a pallet having an expanded polystyrene core and a layer of high impact polystyrene covering a portion of the core.
- U.S. Patent Application Publication No. 2005/0263044 discloses a pallet that includes a shape defining compressible core member, having at least one surface including a convex feature and a core member perimeter; and a thermoplastic shell having a shell interior and a shell edge, where the shell includes a first pliable thermoplastic sheet having an interior shaped by the convex surface of the core member and a first sheet edge extending outside of the core member perimeter, and a second pliable thermoplastic sheet having a second sheet interior and second sheet edge extending outside of the core member perimeter.
- pallets made from plastics are not as strong as traditional wood pallets and, therefore, break under the load-bearing stress applied during use, making them undesirable.
- the present invention provides a load-bearing platform that includes a base and a plurality of legs extending from one side of the base, where the load bearing platform is at least partly made of an expandable polymer matrix that includes an interpolymer of a polyolefin and in situ polymerized vinyl aromatic monomers.
- FIG. 1 is a top perspective view of a load bearing platform according to the invention.
- FIG. 2 is a bottom perspective view of a load bearing platform according to the invention.
- any numerical range recited herein is intended to include all subranges subsumed therein.
- a range of "1 to 10" is intended to include all sub-ranges between and including the recited minimum value of 1 and .the recited maximum value of 10; that is, having a minimum value equal to or greater than 1 and a maximum value of equal to or less than 10.
- the disclosed numerical ranges are continuous, they include every value between the minimum and maximum values. Unless expressly indicated otherwise, the various numerical ranges specified in this application are approximations .
- expandable polymer matrix refers to a polymeric material in particulate or bead form that is impregnated with a blowing agent such that when the particulates and/or beads are placed in a mold and heat is applied thereto, evaporation of the blowing agent (as described below) effects the formation of a cellular structure and/or an expanding cellular structure in the particulates and/or beads and the outer surfaces of the particulates and/or -beads fuse together to form a continuous mass of polymeric material conforming to the shape of the mold.
- polymer is meant to encompass, without limitation, homopolymers, copolymers and graft copolymers.
- polyolefin refers to a polymer prepared from at least one olefinic monomer, such as alpha unsaturated C2-C32 linear or branched alkenes, non-limiting examples of which include ethylene, propylene, 1-butene, 1-hexene and 1-octene.
- polyethylene refers to and includes not only a homopolymer of ethylene, but also an ethylene copolymer containing units of at least 50 mole %, in some cases at least 70 mole %, and in other cases at least 80 mole % of an ethylene unit and a corresponding proportion of units from a monomer copolymerizable with ethylene, and blends containing at least 50% by weight, in some cases at least 60% by- weight, and in other cases at least 75% by weight of an ethylene homopolymer or copolymer with another polymer.
- Non-limiting examples of monomers that can be copolymerized with ethylene include vinyl acetate, vinyl chloride, propylene, 1-butene, 1-hexene, and (meth) acrylic acid and its esters.
- Polymers that can be blended with ethylene homopolymers or copolymers include any polymer compatible with ethylene homopolymers or copolymers.
- Non-limiting examples of polymers that can be blended with ethylene homopolymers or copolymers include polypropylene, polybutadiene, polyisoprene, polychloroprene, chlorinated polyethylene, polyvinyl chloride, styrene/butadiene copolymers, vinyl acetate/ethylene copolymers, acrylonitrile/butadiene copolymers, styrene/butadiene/acrylonitrile copolymers, and vinyl chloride/vinyl acetate copolymer.
- ⁇ > styrenic polymers refers to homopolymers of styrenic monomers and copolymers of styrenic monomers and another copolymerizable monomers, where the styrenic monomers make up at least 50 mole percent of the monomeric units in the copolymer.
- styrenic monomers include styrene, p-methyl styrene, ⁇ -methyl styrene, tertiary butyl styrene, dimethyl styrene, nuclear brominated or chlorinated derivatives thereof and combinations thereof.
- Non-limiting examples of suitable copolymerizable monomers include 1,3- butadiene, C 1 -C 32 linear, cyclic or branched alkyl (meth) acrylates (specific non-limiting examples include butyl (meth) acrylate, ethyl (meth) acrylate, methyl (meth) acrylate, and 2-ethylhexyl (meth) acrylate) , acrylonitrile, vinyl acetate, alpha-methylethylene, divinyl benzene, maleic anhydride, maleic acid, fumaric acid, C3.-C 1 2 linear, branched or cyclic mono- and di- alkyl esters of maleic acid, C 3.
- (meth) acrylic and “ (meth) acrylate” are meant to include both acrylic and methacrylic acid derivatives, such as the corresponding alkyl esters often referred to as acrylates and (meth) acrylates, which the term ⁇ (meth) acrylate” is meant to encompass.
- molding refers to the shaping of a pliable material to assume a new desired shape. Molding can involve the use of specific molding tools such as male and female molding tools, sculptured platens, and the like. It can also include the use of specifically shaped core members including compressible core members that are used to impart a desired shape to at least a portion of a thermoplastic material.
- expansion factor refers to the volume a given weight of expanded polymer bead occupies, typically expressed as cc/g.
- the present invention provides a load-bearing platform that includes a base and a plurality of legs extending from one side of the base.
- the present load-bearing platform is made from an expandable polymer matrix that includes an interpolymer of a polyolefin and in situ polymerized vinyl aromatic monomers and optionally other expandable polymers .
- the interpolymer of a polyolefin and in situ polymerized vinyl aromatic monomers is one or more of those described in U.S. Patent Nos . 3,959,189; 4,168,353; 4,303,756, 4,303,757 and 6,908,949, the relevant portions of which are herein incorporated by reference.
- a non-limiting example of such interpolymers that can be used in the present invention include those available under the trade name ARCEL ® , available from NOVA Chemicals Inc., Pittsburgh, PA and PIOCELAN ® , available from Sekisui Plastics Co., Ltd., Tokyo, Japan.
- the interpolymer of a polyolefin and in situ polymerized vinyl aromatic monomers is a particle or resin bead, which is subsequently processed to form the pallets according to the present invention.
- the interpolymer particles used in the invention include a polyolefin and an in situ polymerized vinyl aromatic resin that form an interpenetrating network of polyolefin and vinyl aromatic resin particles.
- the interpolymer particles are impregnated with a blowing agent and optionally, a plasticizer.
- Such interpolymer particles can be obtained by processes that include suspending polyolefin particles and vinyl aromatic monomer or monomer mixtures in an aqueous suspension and polymerizing the monomer or monomer mixtures inside the polyolefin particles .
- Non- limiting examples of such processes are disclosed in U.S. Pat. Nos. 3,959,189, 4,168,353 and 6,908,949.
- the polyolefin includes one or more polyethylene resins selected from low-, medium-, and high-density polyethylene, an ethylene vinyl acetate copolymer, an ethylene/propylene copolymer, a blend of polyethylene and polypropylene, a blend of polyethylene and an ethylene/vinyl acetate copolymer, and a blend of polyethylene and an ethylene/propylene copolymer.
- Ethylene-butyl acrylate copolymer and ethylene-methyl methacrylate copolymer can also be used.
- the amount of polyolefin in the interpolymer resin particles of the invention can be at least 20%, in some cases at least 25%, and in other cases at least 30% and can be up to 80%, in some cases up to 70%, in other cases up to 60% and in some instances up to 55%, by weight based on the weight of the interpolymer resin particles.
- the amount of polyolefin in the interpolymer resin particles can be any value or range between any of the values recited above.
- the amount of polymerized vinyl aromatic resin in the interpolymer resin particles of the invention ranges can be at least 20%, in some cases at least 30%, in other cases at least 40% and in some instances at least 45% and can be up to 80%, in some cases up to 75% and in other cases up to 70%, by weight based on the weight of the interpolymer resin particles.
- the amount of polymerized vinyl aromatic resin in the interpolymer resin particles can be any value or range between any of the values recited above.
- the vinyl aromatic resin can be made up of polymerized vinyl aromatic monomers or the resin can be a copolymer containing monomeric units from vinyl aromatic monomers and copolymerizable comonomers.
- vinyl aromatic monomers that can be used in the invention include styrene, alpha- methylstyrene, ethylstyrene, chlorostyrene, bromostyrene, vinyltoluene, vinylbenzene, and isopropylxylene . These monomers may be used either alone or in admixture.
- Non-limiting examples of copolymerizable comonomers include 1, 3-butadiene, Ci-C 32 linear, cyclic or branched alkyl (rueth) acrylates (specific non- limiting examples include butyl (meth) acrylate, ethyl (meth) acrylate and 2-ethylhexyl (meth) acrylate) , acrylonitrile, vinyl acetate, alpha-methylethylene, divinyl benzene, maleic anhydride, itaconic anhydride, dimethyl maleate and diethyl maleate.
- Non-limiting examples of vinyl aromatic copolymers that can be used in the invention include those disclosed in U.S. Patent No. 4,049,594.
- Specific non-limiting examples of suitable vinyl aromatic copolymers include copolymers containing repeat units from polymerizing styrene and repeat units from polymerizing one or monomers selected from 1, 3-butadiene, C1-C3 2 linear, cyclic or branched alkyl (meth) acrylates (specific non-limiting examples including butyl (meth) acrylate, ethyl (meth) acrylate and 2-ethylhexyl (meth) acrylate) , acrylonitrile, vinyl acetate, alpha-' methylethylene, divinyl benzene, maleic anhydride, itaconic anhydride, dimethyl maleate and diethyl maleate.
- the vinyl aromatic resin includes polystyrene or styrene- butyl acrylate copolymers.
- the interpolymer resin particles are formed as follows:
- the polyolefin particles are dispersed in an aqueous medium prepared by adding 0.01 to 5%, in some cases 2 to 3%, by weight based on the weight of the water of a suspending agent such as water soluble high molecular weight materials, e.g., polyvinyl alcohol or methyl cellulose or slightly water soluble inorganic materials, e.g., calcium phosphate or magnesium pyrophosphate and soap, such as sodium dodecyl benzene sulfonate, and the vinyl aromatic monomers are added to the suspension and polymerized inside the polyolefin particles.
- a suspending agent such as water soluble high molecular weight materials, e.g., polyvinyl alcohol or methyl cellulose or slightly water soluble inorganic materials, e.g., calcium phosphate or magnesium pyrophosphate and soap, such as sodium dodecyl benzene sulfonate, and the vinyl aromatic
- any conventionally known and commonly used suspending agents for polymerization of vinyl aromatic monomers can be employed. These agents are well known in the art and can be freely selected by one skilled in the art.
- the water is in an amount generally from 0.7 to 5, preferably 3 to 5 times that of the starting polyolefin particles employed in the aqueous suspension, on a weight basis, and gradually the ratio of the polymer particles to the water may reach around 1:1.
- the polymerization of the vinyl aromatic monomers, which is absorbed in the polyolefin particles, is carried out using initiators.
- the initiators suitable for suspension polymerization of the vinyl aromatic monomers are generally used in an amount of about 0.05 to 2 percent by weight, in some cases 0.1 to 1 percent by weight, based on the weight of the vinyl aromatic monomer.
- suitable initiators include organic peroxides such as benzoyl peroxide, lauroyl peroxide, t-butyl perbenzoate and t-butyl perpivalate and azo compounds such as azobisisobutylonitrile and azobisdimethylvaleronitrile.
- initiators can be used alone or two or more initiators can be used in combination.
- the initiators are dissolved in the vinyl aromatic monomers, which are to be absorbed in the polyolefin particles.
- the initiator can be dissolved in a solvent, such as toluene, benzene, and 1 , 2-dichloropropane .
- the polyolefin particles are cross- linked.
- the cross-linking can be accomplished simultaneously with the polymerization of the vinyl aromatic monomer in the polyolefin particles, and before impregnation of the blowing agent and/or plasticizer.
- cross-linking agents are used.
- Such cross-linking agents include, but are not limited to di-t-butyl-peroxide, t-butyl-cumylperoxide, dicumyl-peroxide, .alpha,, . alpha.
- cross-linking agents are absorbed in the polyolefin particles together with the vinyl aromatic monomers by dissolving the cross-linking agent in an amount of about 0.1 to 2 weight % and in some cases 0.5 to 1 weight %, based on the weight of the polyolefin particles suspended in water. Further details of the cross-linking agents and the manner for absorbing the cross-linking agents into the polyolefin particles are provided in U.S. Patent No. 3,959,189.
- the interpolymer of a polyolefin and in situ polymerized vinyl aromatic monomers includes a rubber modified styrenic polymer where the rubber constitutes a continuous phase and the styrenic polymer constitutes a dispersed phase in the resin as described in copending U.S. Patent Application Publication No. 2006/0276558, the relevant portions of which are herein incorporated by reference.
- the rubber modified styrenic polymers are prepared by:
- a dispersion of organic droplets is formed by pressure atomizing an organic phase below the free surface of an aqueous phase, which can be stationary or flowing.
- a dispersion of organic droplets of an organic liquid phase in an aqueous phase is formed by applying mechanical agitation.
- the styrenic polymers can include residues from the polymerization of vinyl aromatic monomers selected from styrene, alpha-methylstyrene, ethylstyrene, chlorostyrene, bromostyrene, vinyltoluene, vinylbenzene, and isopropylxylene and admixtures thereof.
- the elastomeric polymers can include copolymers of one or more conjugated dienes such as but not limited to butadiene, isoprene (i.e., 2-methyl-l, 3-butadiene) , 3-butadiene, 2, 3-dimethyl-l, 3-butadiene and 1,3- pentadiene, one or more of a suitable unsatured nitrile such as acrylonitrile or methacrylonitiles and optionally one or more of a polar monomer such as acrylic acid, methacrylic acid, itaconic acid and maleic acid, alkyl esters of unsaturated carboxylic acids such as methyl acrylate and butyl acrylate; alkoxyalkyl esters of unsaturated carboxylic acids such as n ⁇ ethoxy acrylate, ethoxyethyl acrylate, methoxyethyl acrylate, acrylamide, methacrylamide; N-substituted acrylamides such as N-methyl
- copolymers can also include repeat units from the polymerization of one or more aromatic vinyl monomers such as but not limited to styrene, 0-, m ⁇ , p-methyl styrene, dimethylstyrene and ethyl styrene.
- aromatic vinyl monomers such as but not limited to styrene, 0-, m ⁇ , p-methyl styrene, dimethylstyrene and ethyl styrene.
- acrylonitrile- butadiene rubbers or “acrylonitrile-butadiene-styrene rubbers” or collectively as “nitrile rubbers” by those skilled in the art.
- the nitrile rubbers can be partially hydrogenated in the presence of hydrogen, preferably with a suitable hydrogenation catalyst.
- the expandable polymer matrix of the invention can be used as raw materials in producing foamed articles.
- the blowing agent and/or plasticizer are introduced into the expandable polymer matrix resin particles to form foamable or expandable particles or resin beads, which in turn, are used to mold foamed articles.
- the blowing agent should have a boiling point lower than the softening point of the polyolefin and should be gaseous or liquid at room temperature (about 20 to 30 0 C) and normal pressure (about atmospheric) . Blowing agents are well known in the art and generally have boiling points ranging from -42°C to 80 0 C, more generally, from -10 0 C to 36°C.
- Suitable hydrocarbon blowing agents include, but are not limited to aliphatic hydrocarbons such as n- ⁇ ropane 7 n-butane, iso-butane, n-pentane, iso-pentane, n-hexane, and neopentane, cycloaliphatic hydrocarbons such as cyclobutane and cyclopentane, and halogenated hydrocarbons such as methyl chloride, ethyl chloride, methylene chloride, trichlorofluoromethane, dischloro- fluoromethane, dichlorodifluormethane, chlorodifluoromethane and dichlorotetrafluoroethane, etc.
- aliphatic hydrocarbons such as n- ⁇ ropane 7 n-butane, iso-butane, n-pentane, iso-pentane, n-hexane, and neopent
- blowing agents can be used alone or as mixtures. If n- butane, ethyl chloride, and dichlorotetrafluoroethane, which are gaseous at room temperature and normal pressure, are used as a mixture, it is possible to achieve foaming to a low bulk density. Specific types of volatile blowing agents are taught in U.S. Patent No. 3,959,180. In particular embodiments of the invention/ the blowing agent is selected from n- pentane, iso-pentane, neopentane, cylcopentane, and mixtures thereof.
- the amount of the blowing agent ranges from about 1.5% to about 20% by weight, in some cases about 1.5% to 15% by weight, and in other cases from 5% to 15% by weight, based on the weight of the expandable polymer matrix.
- a plasticizer can be used in. combination with the blowing agent and as stated herein above and acts as a blowing aid in the invention.
- Suitable plasticizers include, but are not limited to benzene, toluene, limonene, linear, branched or cyclic C 5 to C 20 alkanes, white oil, linear, branched or cyclic Ci to C 2 O dialkylphthalates, styrene, oligomers of styrene, oligomers of (meth) acrylates having a glass transition temperature less than polystyrene, and combinations thereof.
- the plasticizer includes limonene, a mono-terpene hydrocarbon existing widely in the plant world.
- the known types are d-limonene, 1-limonene, and dl- limonene.
- D-limonene is contained in the skin of citrus fruits and is used in food additives as a fragrant agent; its boiling point is about 176°C; and its flammability is low.
- D-limonene is a colorless liquid, has a pleasant orange-like aroma, is approved as a food additive, and is widely used as a raw material of perfume.
- Limonene is not a hazardous air pollutant.
- the amount of plasticizer can range from about 0.1 to 5 parts and in some cases from about 0.1 to about 1 part, by weight per 100 parts by weight of the expandable polymer matrix.
- the interpolymer particles can be produced as follows: In a first reactor, the polyolefin particles are suspended in an aqueous medium containing a dispersing agent.
- the dispersing agent can be polyvinyl alcohol, methylcellulose, calcium phosphate, magnesium pyrophosphate, calcium carbonate, tricalcium phosphate, etc.
- the amount of dispersing agent employed can be from 0.01 to 5% by weight based on the amount of water.
- A- surfactant can be added to the aqueous medium. Generally, the surfactant is used to lower the surface tension of the suspension and helps to emulsify the water/vinyl aromatic monomer in mixture in the initiator and wax mixes, if used.
- Suitable waxes include polyethylene waxes and ethylene bistearamide.
- the aqueous medium is generally heated to a temperature at which the vinyl aromatic monomers can be polymerized, i.e., from about 60 0 C to about 120 0 C over a period of time, for example, 12 to 20 hours. Over this 12 to 20 hour period, the vinyl aromatic monomers, the vinyl aromatic polymerization initiator, and the cross-linking agent are added to the resulting suspension containing the polyolefin particles, which are dispersed in the aqueous medium. These materials may be added all at one time, or gradually in individual portions.
- the interpolymer particles are acidified, dewatered, screened, and subsequently charged to a second reactor where the particles are impregnated with the blowing agent and/or plasticizer.
- the impregnation step can be carried out by suspending the interpolymer particles in an aqueous medium, adding the blowing agent and/or plasticizer to the resulting suspension, and stirring at a temperature of, preferably, about 40 0 C degrees to 80 0 C.
- the blowing agent and/or plasticizer can be blended together and then added to the interpolymer particles or .can be added to the interpolymer particles separately.
- blowing agent and/or plasticizer can be added to the first reactor during or after the polymerization process.
- the above processes describe a wet process for impregnation of the interpolymer particles.
- the interpolymer particles can be impregnated via an anhydrous process similar to that taught in Column 4, lines 20-36 of U.S. Patent No. 4,429,059.
- the blowing agent can be dosed to the expandable polymer matrix in an extruder to produce resin pellets or beads.
- the extruder acts to mix the blowing agent into the expandable polymer matrix prior to extruding a strand of the mixture.
- the strand can be cut into bead or pellet lengths using an appropriate device, a non- limiting example being an underwater face cutter.
- the interpolymer resin and/or expandable polymer matrix particles can also contain other additives known in the art, non-limiting examples including anti-static additives; flame retardants; colorants or dyes; filler materials and combinations thereof.
- Other additives can also include chain transfer agents, non-limiting examples including C2-15 alkyl mercaptans, such as n- dodecyl mercaptan, t-dodecyl mercaptan, t-butyl mercaptan and n-butyl mercaptan, and other agents such as pentaphenyl ethane and the dimer of alpha-methyl styrene .
- Other additives can further include nucleating agents, non-limiting examples including polyolefin waxes, i.e., polyethylene waxes.
- the expandable polymer matrix includes interpolymers of a polyolefin and in situ polymerized vinyl aromatic monomers and optionally other expandable polymers.
- the other expandable polymers include those polymers that can provide desirable properties to the load bearing platform of the invention and that are compatible with the interpolymers of a polyolefin and in situ polymerized vinyl aromatic monomers.
- Non- limiting examples of other expandable polymers that can be used in the present invention include expandable polystyrene (EPS) , expandable polyolefins, rubber modified styrenic polymers where the styrenic polymer constitutes a continuous phase and the rubber constitutes a dispersed phase in the resin, rubber modified styrenic polymers where the rubber constitutes a continuous phase and the styrenic polymer constitutes a dispersed phase in the resin as described in copending U.S. Patent Application Publication No. 2006/0276558, the relevant portions of which are herein incorporated by reference, polyphenylene oxide, and combinations and blends thereof.
- EPS expandable polystyrene
- expandable polyolefins rubber modified styrenic polymers where the styrenic polymer constitutes a continuous phase and the rubber constitutes a dispersed phase in the resin
- rubber modified styrenic polymers where the rubber constitutes a continuous phase and
- the expandable polymer matrix can contain 100% interpolymers of a polyolefin and in situ polymerized vinyl aromatic monomers, but can also contain up to 99%, in some cases up to 95%, in other cases up to 90%, in some instances up to 80% and in other instances up to 75% based on the weight of the expandable polymer matrix of interpolymers of a polyolefin and in situ polymerized vinyl aromatic monomers. Also, the expandable polymer matrix can contain at least 25%, in some cases at least 30%, in other cases at least 40% and in some instances at least 50% based on the weight of the expandable polymer matrix of interpolymers of a polyolefin and in situ polymerized vinyl aromatic monomers.
- the amount of interpolymers of a polyolefin and in situ polymerized vinyl aromatic monomers in the expandable polymer matrix can be any value or range between any of the values recited above.
- the other expandable polymers can be present at a level of at least 1%, in some cases at least 5%, in other cases at least 10%, in some instances at least 20% and in other instances at least 25% based on the weight of the expandable polymer matrix.
- the other expandable polymers can be present in the expandable polymer matrix at a level of up to 75%, in some cases up to 70%, in other cases up to 60% and in some instances up to 50% based on the weight of the expandable polymer matrix.
- the other expandable polymers can be included in the expandable polymer matrix at any level or range between any of the values recited above.
- a load bearing structure 8 includes an expanded polymer matrix core 10, which is in the general shape of a rectangular slab with an edge 12 that has a width 14 which can be from 1 to 25 cm, in some cases from 2 to.20 cm and in other cases from 2.5 to 15 cm.
- Core 10 has a topside 16 that can be from 75 to 150 cm, in some cases from 90 to 140 cm and in other cases from 100 to 130 cm long and from 65 to 140 cm, in some cases from 80 to 130 cm and in other cases from 90 to 120 cm forty inches wide.
- a bottom side 18 of core 10 includes legs 20-28 from 8 to 15 cm, in some cases from 9 to 13 cm long extending from bottom side 10.
- Legs 20-28 and bottom side 18 define spaces 42, 44, 46, and 48 proximate to edge 12. Spaces 42, 44, 46, 48 separate legs 26-28, legs 20, 23, 26, legs 20-22 and legs 22, 25, 28, respectively, from the edge 12. In an embodiment of the invention, spaces 42, 44, 46, 48 are adapted to receive the tongues of a forklift truck.
- a first tongue of a forklift can be placed under and along the length of bottom side 18 between leg 20 and leg 23, leg 21 and leg 24 and/or between leg 22 and leg 25 and a second tongue of a forklift can be placed under and along the length of bottom side 18 between leg 26 and leg 23, leg 27 and leg 24 and/or between leg 28 and leg 25.
- a surface of each tongue contacts the surface of bottom side 18 and acts to lift load bearing structure 8 and any articles stacked on topside 16.
- core 10 is made from the above-described expanded polymer matrix, it has sufficient structural strength to be used as a load bearing platform.
- Suitable layer materials that can be applied include rubber modified styrenic polymers, polyamides, such as nylon, polypropylene, polyethylene, and combinations thereof.
- the density of the expanded polymer matrix in core 10 can be at least 5, in some cases at least 10 and in other cases at least 15 kg/m 3 and can be up to 40, in some cases up to 35 and in other cases up to 30 kg/m 3 .
- the density of the expanded polymer matrix in core 10 corresponding to the portions proximate spaces 42, 44, 46, 48 is higher than the density of the expanded polymer matrix in the remainder of core 10. This feature aids in preventing stress breakage at the thinnest portions of load bearing structure 8.
- the load bearing structure can be prepared by heating beads of the expandable polymer matrix using a heating medium such as steam. Depending on the desired density in any portion of the load bearing structure, the beads are expanded to an expansion ratio (the ratio of expanded bead volume/initial bead volume) of from 5 to 100, in some cases from 10 to 90, in other cases from 20 to 80, in some instances from 30 to 75 and in other instances from 40 to 70.
- an expansion ratio the ratio of expanded bead volume/initial bead volume
- the beads of the expandable polymer matrix according to the invention can be formed into a load bearing structure of a desired configuration by pre- expanding the beads and further expanding and shaping them in a mold cavity.
- the resulting load bearing structure has superior thermal stability, chemical resistance (e.g., oil resistance), and flexural strength compared to EPS pallets.
- a groove or channel can be molded or cut into the surface of topside 16 such that the groove or channel follows the perimeter of topside 16 and a first edge of the groove or channel is spaced apart from edge 12.
- the spacing of the groove or channel from edge 12 can be at least 1 cm, in some cases at least 2 cm and can be up to 10 cm, in some cases up to 8 cm.
- the groove or channel can be continuous or discontinuous .
- the groove or channel has a width ' and depth adapted to receive a foam panel.
- the foam panel can form an angle or arc to conform to a corner section of topside 16 directly above a portion of leg 20, 22, 28 and/or 26.
- the foam panel can extend along the sides of topside 16 beginning above leg 20 and terminating above leg 22, beginning above leg 22 and terminating above leg 28, beginning above leg 28 and terminating above leg 26, and/or beginning above leg 26 and terminating above leg 20.
- the length of the panels will conform to the dimensions of load bearing platform 8 as described above.
- the height of the panels can be at least 5 cm, in some cases at least 10 cm and in other cases at least 15 cm and can be up to 450 cm, in some cases up to 400 cm, in other cases up to 350 cm and in some instances up to 310 cm.
- the height of the panels can be any value or range between any of the values recited above.
- a top panel can be included that roughly matches the width and length of load bearing structure 8.
- the top panel includes a groove or channel matching the groove or channel in topside 16 and is adapted to receive a top surface of the panels.
- the load bearing structure, panels and top panel When assembled, the load bearing structure, panels and top panel form a box or open-box structure. Buckles or appropriate fasteners can be used to secure the panels and structure together. Alternatively, shrink wrap can be applied around the outside perimeter of the box or open-box structure to secure the parts in position.
- the top panel can be a load bearing structure 8 that includes a groove or channel that passes along a corresponding bottom surface of legs 20, 21, 22, 25, 28, 27, 26, and/or 23.
- the panels and top panels are made from the expandable polymer matrix described herein.
- the panels and top panels are made of one or more other expandable polymers as described above.
- the panels and/or top panel prevent articles placed or stacked on topside 16 from sliding or otherwise leaving the surface of topside 16 when load bearing structure 8 is moved.
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- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
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Applications Claiming Priority (2)
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US80116706P | 2006-05-17 | 2006-05-17 | |
PCT/US2007/010406 WO2007136514A1 (en) | 2006-05-17 | 2007-04-30 | Load bearing structure |
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US7494298B2 (en) | 2006-06-28 | 2009-02-24 | Bbl Falcon Industries, Ltd | Method of constructing a secondary containment area |
US20090120823A1 (en) * | 2007-11-13 | 2009-05-14 | Airdex International, Inc. | Tray pallet |
US8734052B2 (en) | 2008-10-20 | 2014-05-27 | Falcon Technologies And Services, Inc. | Tank base |
CA2751757A1 (en) * | 2009-02-03 | 2010-08-12 | Miller Dowel Company | Beveled block pallet |
CA2816117C (en) * | 2010-11-01 | 2019-04-02 | Stellar Field Corp. | Pallet stacking board construction |
US9796503B2 (en) * | 2015-07-17 | 2017-10-24 | Christopher W. Gabrys | Corrugated skid |
USD773012S1 (en) | 2014-09-12 | 2016-11-29 | Falcon Technologies And Services, Inc. | Tank base |
US9908692B2 (en) | 2015-05-06 | 2018-03-06 | ASFI Partners, L.P. | Multi-piece storage tank pad with separate connectors |
US10683135B2 (en) | 2015-07-17 | 2020-06-16 | Christopher W. Gabrys | Corrugated skid with optimum support |
MY193282A (en) * | 2015-12-16 | 2022-09-30 | Airdex Corp | Load bearing structure |
US10518931B2 (en) * | 2017-05-11 | 2019-12-31 | Lesweek Pty Ltd | Load bearing structure |
US11021295B2 (en) * | 2015-12-16 | 2021-06-01 | Lesweek Pty Ltd | Load bearing structure |
US10495172B2 (en) | 2017-06-06 | 2019-12-03 | Asset Guard Products Inc. | Equipment platform |
USD869812S1 (en) * | 2017-11-03 | 2019-12-10 | Inteplast Group Corporation | Pallet |
USD951581S1 (en) * | 2019-05-15 | 2022-05-10 | Chep Technology Pty Limited | Part for a pallet |
JP2023015433A (ja) * | 2021-07-20 | 2023-02-01 | 富士フイルムビジネスイノベーション株式会社 | パレット |
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US3511191A (en) * | 1968-06-28 | 1970-05-12 | Foster Grant Co Inc | Pallets |
US4233418A (en) * | 1978-05-31 | 1980-11-11 | Cosden Technology, Inc. | Process for preparing rubber-modified styrene copolymers by suspension copolymerization |
US4809618A (en) * | 1988-03-21 | 1989-03-07 | Bell Joseph P | Plastic pallet |
US5945147A (en) * | 1997-10-23 | 1999-08-31 | Cold-Bag, Inc. | Method for packaging fresh perishable foods |
US6955128B2 (en) * | 2001-10-19 | 2005-10-18 | Rehrig Pacific Company | Reinforced pallet |
US6908949B2 (en) * | 2003-01-27 | 2005-06-21 | Nova Chemicals Inc. | Foamable interpolymer resin particles containing limonene as a blowing aid |
US20050126448A1 (en) * | 2003-12-12 | 2005-06-16 | David Bernstein | Modular pallet |
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2007
- 2007-04-30 AU AU2007254449A patent/AU2007254449A1/en not_active Abandoned
- 2007-04-30 WO PCT/US2007/010406 patent/WO2007136514A1/en active Application Filing
- 2007-04-30 US US11/796,908 patent/US20070283856A1/en not_active Abandoned
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AU2007254449A1 (en) | 2007-11-29 |
BRPI0712038A2 (pt) | 2011-12-20 |
CA2650615A1 (en) | 2007-11-29 |
MX2008014417A (es) | 2008-11-27 |
WO2007136514A1 (en) | 2007-11-29 |
KR20090020619A (ko) | 2009-02-26 |
JP2009537407A (ja) | 2009-10-29 |
CN101443185A (zh) | 2009-05-27 |
US20070283856A1 (en) | 2007-12-13 |
TW200812801A (en) | 2008-03-16 |
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