NZ566362A - Intercalated layered silicate - Google Patents
Intercalated layered silicateInfo
- Publication number
- NZ566362A NZ566362A NZ566362A NZ56636206A NZ566362A NZ 566362 A NZ566362 A NZ 566362A NZ 566362 A NZ566362 A NZ 566362A NZ 56636206 A NZ56636206 A NZ 56636206A NZ 566362 A NZ566362 A NZ 566362A
- Authority
- NZ
- New Zealand
- Prior art keywords
- layered silicate
- silicate
- dispersed
- intercalated layered
- film
- Prior art date
Links
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 title claims abstract description 141
- 239000002245 particle Substances 0.000 claims abstract description 81
- 239000000203 mixture Substances 0.000 claims abstract description 76
- -1 fatty acid esters Chemical class 0.000 claims abstract description 71
- 239000010410 layer Substances 0.000 claims abstract description 70
- 239000011159 matrix material Substances 0.000 claims abstract description 60
- 239000000138 intercalating agent Substances 0.000 claims abstract description 46
- 238000000034 method Methods 0.000 claims abstract description 24
- 235000013305 food Nutrition 0.000 claims abstract description 18
- 239000011229 interlayer Substances 0.000 claims abstract description 18
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 16
- 239000000194 fatty acid Substances 0.000 claims abstract description 16
- 229930195729 fatty acid Natural products 0.000 claims abstract description 16
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims abstract description 12
- 150000002194 fatty esters Chemical class 0.000 claims abstract description 8
- 238000002156 mixing Methods 0.000 claims abstract description 8
- 229920000223 polyglycerol Polymers 0.000 claims abstract description 8
- 238000004806 packaging method and process Methods 0.000 claims abstract description 4
- 229920000642 polymer Polymers 0.000 claims description 58
- 229920001577 copolymer Polymers 0.000 claims description 51
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 37
- 239000005977 Ethylene Substances 0.000 claims description 36
- 239000002243 precursor Substances 0.000 claims description 21
- 239000004952 Polyamide Substances 0.000 claims description 18
- 229920002647 polyamide Polymers 0.000 claims description 18
- 238000000576 coating method Methods 0.000 claims description 17
- 239000002537 cosmetic Substances 0.000 claims description 17
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- 239000011248 coating agent Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- 229920000728 polyester Polymers 0.000 claims description 13
- 239000002904 solvent Substances 0.000 claims description 13
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 11
- 229920001169 thermoplastic Polymers 0.000 claims description 10
- 150000003868 ammonium compounds Chemical class 0.000 claims description 9
- 239000011230 binding agent Substances 0.000 claims description 9
- 239000012785 packaging film Substances 0.000 claims description 9
- 229920006280 packaging film Polymers 0.000 claims description 9
- 235000021485 packed food Nutrition 0.000 claims description 9
- 239000004519 grease Substances 0.000 claims description 8
- 229920000554 ionomer Polymers 0.000 claims description 8
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 7
- 229920000098 polyolefin Polymers 0.000 claims description 7
- 239000004416 thermosoftening plastic Substances 0.000 claims description 7
- 239000004793 Polystyrene Substances 0.000 claims description 6
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 6
- 229920002223 polystyrene Polymers 0.000 claims description 6
- 229940124531 pharmaceutical excipient Drugs 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical class CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 claims description 4
- 239000003974 emollient agent Substances 0.000 claims description 4
- 239000003349 gelling agent Substances 0.000 claims description 4
- 239000003906 humectant Substances 0.000 claims description 4
- 150000002632 lipids Chemical class 0.000 claims description 4
- 239000010687 lubricating oil Substances 0.000 claims description 4
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical class FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 claims description 3
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical class CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- 239000008407 cosmetic solvent Substances 0.000 claims description 2
- 239000007764 o/w emulsion Substances 0.000 claims description 2
- 239000007762 w/o emulsion Substances 0.000 claims description 2
- 238000010998 test method Methods 0.000 claims 1
- 239000010408 film Substances 0.000 description 88
- 150000001875 compounds Chemical class 0.000 description 17
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 15
- 239000000178 monomer Substances 0.000 description 15
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 11
- 229920002302 Nylon 6,6 Polymers 0.000 description 10
- 150000002148 esters Chemical class 0.000 description 10
- 239000000976 ink Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- 238000004299 exfoliation Methods 0.000 description 8
- 230000008569 process Effects 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 7
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 238000007789 sealing Methods 0.000 description 7
- 150000004760 silicates Chemical class 0.000 description 7
- 229920002292 Nylon 6 Polymers 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 6
- 150000004985 diamines Chemical class 0.000 description 6
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 6
- 238000006068 polycondensation reaction Methods 0.000 description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000001993 wax Substances 0.000 description 6
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 5
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 5
- 150000008064 anhydrides Chemical group 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- 239000002552 dosage form Substances 0.000 description 5
- UFRKOOWSQGXVKV-UHFFFAOYSA-N ethene;ethenol Chemical compound C=C.OC=C UFRKOOWSQGXVKV-UHFFFAOYSA-N 0.000 description 5
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 229920000139 polyethylene terephthalate Polymers 0.000 description 5
- 239000005020 polyethylene terephthalate Substances 0.000 description 5
- 239000004800 polyvinyl chloride Substances 0.000 description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
- 230000005855 radiation Effects 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 4
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- TVIDDXQYHWJXFK-UHFFFAOYSA-N dodecanedioic acid Chemical compound OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 4
- 229920001038 ethylene copolymer Polymers 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- 238000009830 intercalation Methods 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid Substances OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 125000001453 quaternary ammonium group Chemical group 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- DJZKNOVUNYPPEE-UHFFFAOYSA-N tetradecane-1,4,11,14-tetracarboxamide Chemical compound NC(=O)CCCC(C(N)=O)CCCCCCC(C(N)=O)CCCC(N)=O DJZKNOVUNYPPEE-UHFFFAOYSA-N 0.000 description 4
- 239000002966 varnish Substances 0.000 description 4
- 229920001567 vinyl ester resin Polymers 0.000 description 4
- 239000004711 α-olefin Substances 0.000 description 4
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000004953 Aliphatic polyamide Substances 0.000 description 3
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229920006257 Heat-shrinkable film Polymers 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 229920000305 Nylon 6,10 Polymers 0.000 description 3
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 3
- 229920003231 aliphatic polyamide Polymers 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 230000002687 intercalation Effects 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 150000004714 phosphonium salts Chemical class 0.000 description 3
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- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- FUSNPOOETKRESL-ZPHPHTNESA-N (z)-n-octadecyldocos-13-enamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCC\C=C/CCCCCCCC FUSNPOOETKRESL-ZPHPHTNESA-N 0.000 description 2
- LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 description 2
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- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
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- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 2
- VYWRBUBXZALATG-UHFFFAOYSA-N 2-hydroxyoctadecanamide Chemical compound CCCCCCCCCCCCCCCCC(O)C(N)=O VYWRBUBXZALATG-UHFFFAOYSA-N 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
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- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
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- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
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- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
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- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
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- 238000000354 decomposition reaction Methods 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
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- 239000002985 plastic film Substances 0.000 description 2
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- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
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- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- 230000000699 topical effect Effects 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
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- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
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- VJESJEJNMGVQLZ-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)N(CCO)CCO VJESJEJNMGVQLZ-UHFFFAOYSA-N 0.000 description 1
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- SKDZEPBJPGSFHS-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)tetradecanamide Chemical compound CCCCCCCCCCCCCC(=O)N(CCO)CCO SKDZEPBJPGSFHS-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- DJWFNQUDPJTSAD-UHFFFAOYSA-N n-octadecyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCCNC(=O)CCCCCCCCCCCCCCCCC DJWFNQUDPJTSAD-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
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- FCZSASCJWJQESY-UHFFFAOYSA-N octadecyl(triphenyl)phosphanium Chemical class C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CCCCCCCCCCCCCCCCCC)C1=CC=CC=C1 FCZSASCJWJQESY-UHFFFAOYSA-N 0.000 description 1
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- 229910052615 phyllosilicate Inorganic materials 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229920006115 poly(dodecamethylene terephthalamide) Polymers 0.000 description 1
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- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
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- 235000015277 pork Nutrition 0.000 description 1
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- DCBSHORRWZKAKO-UHFFFAOYSA-N rac-1-monomyristoylglycerol Chemical compound CCCCCCCCCCCCCC(=O)OCC(O)CO DCBSHORRWZKAKO-UHFFFAOYSA-N 0.000 description 1
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- HISNRBVYBOVKMB-UHFFFAOYSA-N stibonium Chemical class [SbH4+] HISNRBVYBOVKMB-UHFFFAOYSA-N 0.000 description 1
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- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical class C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- WFIYFFUAOQKJJS-UHFFFAOYSA-N tetraoctylphosphanium Chemical class CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC WFIYFFUAOQKJJS-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/20—Silicates
- C01B33/36—Silicates having base-exchange properties but not having molecular sieve properties
- C01B33/38—Layered base-exchange silicates, e.g. clays, micas or alkali metal silicates of kenyaite or magadiite type
- C01B33/44—Products obtained from layered base-exchange silicates by ion-exchange with organic compounds such as ammonium, phosphonium or sulfonium compounds or by intercalation of organic compounds, e.g. organoclay material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/261—In terms of molecular thickness or light wave length
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Cosmetics (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Aftertreatments Of Artificial And Natural Stones (AREA)
- Medicinal Preparation (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
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| US71001505P | 2005-08-19 | 2005-08-19 | |
| PCT/US2006/031839 WO2007024564A1 (en) | 2005-08-19 | 2006-08-15 | Intercalated layered silicate |
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| NZ566362A true NZ566362A (en) | 2010-11-26 |
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| NZ566362A NZ566362A (en) | 2005-08-19 | 2006-08-15 | Intercalated layered silicate |
| NZ565874A NZ565874A (en) | 2005-08-19 | 2006-08-15 | Film comprising silicate platelets exfoliated from phospholipid-intercalated layered silicate |
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| NZ565874A NZ565874A (en) | 2005-08-19 | 2006-08-15 | Film comprising silicate platelets exfoliated from phospholipid-intercalated layered silicate |
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| US (2) | US20090297568A1 (enExample) |
| EP (3) | EP2105411B1 (enExample) |
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| CA (2) | CA2618863C (enExample) |
| DE (2) | DE602006007015D1 (enExample) |
| NZ (2) | NZ566362A (enExample) |
| WO (2) | WO2007024576A1 (enExample) |
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| EP2072030A1 (en) * | 2007-12-20 | 2009-06-24 | 3M Innovative Properties Company | Dental impression material containing rheological modifiers |
| FR2974497A1 (fr) * | 2011-04-27 | 2012-11-02 | Centre Nat Rech Scient | Prothese de disque intervertebral en materiau thermoplastique a gradient de proprietes mecaniques |
| FR2976503A1 (fr) * | 2011-06-14 | 2012-12-21 | Ephyla | Utilisation de phyllosilicates modifies par des corps gras pour generer des emulsions a froid. |
| US20120328754A1 (en) | 2011-06-21 | 2012-12-27 | Cryovac, Inc. | Impact-Modified Polypropylene Composite |
| CN104853816A (zh) * | 2012-10-12 | 2015-08-19 | 纳幕尔杜邦公司 | 离聚物复合材料 |
| CN103647025A (zh) * | 2013-10-31 | 2014-03-19 | 京东方科技集团股份有限公司 | 复合膜及其制造方法和封装结构 |
| US20170182726A1 (en) * | 2015-12-23 | 2017-06-29 | Dixie Consumer Products Llc | Methods for making paperboard containers from paperboard blanks having shrinkable films secured thereto |
| US10799429B2 (en) * | 2016-02-25 | 2020-10-13 | 3M Innovative Properties Company | Kit of parts for producing a paste type glass ionomer cement, process of production and use thereof |
| US11000148B2 (en) | 2016-06-28 | 2021-05-11 | Berry Plastics Corporation | Beverage-brewing package |
| AU2018304519A1 (en) * | 2017-07-19 | 2020-02-20 | Cryovac, Llc | Antimicrobial packaging films |
| GB201809708D0 (en) | 2018-06-13 | 2018-08-01 | Obrist Closures Switzerland | Beverage capsule |
| CN114929280A (zh) * | 2019-08-20 | 2022-08-19 | 特库瓦兹健康服务医疗清洁化学品产业和贸易有限公司 | 用于生产含生物活性成分的纳米复合物和含生物活性成分的蒙脱石基纳米复合物的方法 |
| US12325579B2 (en) | 2020-10-22 | 2025-06-10 | Berry Global, Inc. | Beverage capsule cup with enhanced material distribution |
| USD981844S1 (en) | 2020-11-25 | 2023-03-28 | Berry Global, Inc. | Beverage capsule cup |
| EP4234492A1 (en) * | 2022-02-23 | 2023-08-30 | ImerTech SAS | Modified clay |
| WO2025075544A1 (en) * | 2023-10-05 | 2025-04-10 | Cropcision Ab | Particle for delayed release of an active ingredient to a plant or seed |
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| US4048378A (en) * | 1976-12-08 | 1977-09-13 | Browne Packaging, Inc. | Adhesive laminated packaging materials |
| US4157375A (en) | 1977-12-02 | 1979-06-05 | Engelhard Minerals & Chemicals Corporation | Conversion of nitrogen oxides |
| US4506048A (en) | 1981-08-07 | 1985-03-19 | The Procter & Gamble Company | Agents for preparing cross-linked polymers and paint and plastic compositions containing those agents |
| JPH0659397B2 (ja) * | 1985-10-11 | 1994-08-10 | 有限会社三好化成 | 表面処理粉体及びその製造方法 |
| US4737295A (en) | 1986-07-21 | 1988-04-12 | Venture Chemicals, Inc. | Organophilic polyphenolic acid adducts |
| JPS6341508A (ja) | 1986-08-07 | 1988-02-22 | Sunstar Giken Kk | 紫外線硬化性組成物 |
| CS263659B1 (cs) | 1986-11-24 | 1989-04-14 | Valenta Vitezslav | Kontinuálnímikroextraktorpro izolaci a zakoncentrovánfcizorodých látek z průtočně vodnífáze |
| US4931195A (en) | 1987-07-15 | 1990-06-05 | Colgate-Palmolive Company | Low viscosity stable non-aqueous suspension containing organophilic clay and low density filler |
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-
2006
- 2006-08-15 EP EP09009227A patent/EP2105411B1/en not_active Not-in-force
- 2006-08-15 US US11/990,734 patent/US20090297568A1/en not_active Abandoned
- 2006-08-15 WO PCT/US2006/031889 patent/WO2007024576A1/en not_active Ceased
- 2006-08-15 AT AT06801527T patent/ATE444986T1/de not_active IP Right Cessation
- 2006-08-15 DE DE602006007015T patent/DE602006007015D1/de active Active
- 2006-08-15 AU AU2006283679A patent/AU2006283679B2/en not_active Ceased
- 2006-08-15 CA CA2618863A patent/CA2618863C/en not_active Expired - Fee Related
- 2006-08-15 US US11/990,614 patent/US8362134B2/en not_active Expired - Fee Related
- 2006-08-15 DE DE602006009693T patent/DE602006009693D1/de active Active
- 2006-08-15 AU AU2006283666A patent/AU2006283666B2/en not_active Ceased
- 2006-08-15 NZ NZ566362A patent/NZ566362A/en not_active IP Right Cessation
- 2006-08-15 EP EP06801563A patent/EP1924527B1/en not_active Not-in-force
- 2006-08-15 NZ NZ565874A patent/NZ565874A/en not_active IP Right Cessation
- 2006-08-15 AT AT06801563T patent/ATE432241T1/de not_active IP Right Cessation
- 2006-08-15 CA CA2619072A patent/CA2619072C/en not_active Expired - Fee Related
- 2006-08-15 AT AT09009227T patent/ATE549296T1/de active
- 2006-08-15 WO PCT/US2006/031839 patent/WO2007024564A1/en not_active Ceased
- 2006-08-15 EP EP06801527A patent/EP1945706B1/en not_active Not-in-force
- 2006-08-15 JP JP2008527076A patent/JP5358183B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2618863C (en) | 2011-03-15 |
| AU2006283666B2 (en) | 2011-04-21 |
| WO2007024576A1 (en) | 2007-03-01 |
| EP2105411B1 (en) | 2012-03-14 |
| EP1924527B1 (en) | 2009-05-27 |
| DE602006009693D1 (de) | 2009-11-19 |
| DE602006007015D1 (de) | 2009-07-09 |
| EP2105411A1 (en) | 2009-09-30 |
| US20090297675A1 (en) | 2009-12-03 |
| ATE432241T1 (de) | 2009-06-15 |
| EP1924527A1 (en) | 2008-05-28 |
| JP2009504886A (ja) | 2009-02-05 |
| ATE444986T1 (de) | 2009-10-15 |
| CA2619072C (en) | 2011-03-15 |
| EP1945706A1 (en) | 2008-07-23 |
| JP5358183B2 (ja) | 2013-12-04 |
| US8362134B2 (en) | 2013-01-29 |
| CA2619072A1 (en) | 2007-03-01 |
| CA2618863A1 (en) | 2007-03-01 |
| ATE549296T1 (de) | 2012-03-15 |
| EP1945706B1 (en) | 2009-10-07 |
| WO2007024564A1 (en) | 2007-03-01 |
| NZ565874A (en) | 2010-11-26 |
| AU2006283679B2 (en) | 2011-05-19 |
| AU2006283666A1 (en) | 2007-03-01 |
| US20090297568A1 (en) | 2009-12-03 |
| AU2006283679A1 (en) | 2007-03-01 |
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| PSEA | Patent sealed | ||
| RENW | Renewal (renewal fees accepted) | ||
| LAPS | Patent lapsed |