AU2005243273B2 - Metal phosphonates and related nanocomposites - Google Patents
Metal phosphonates and related nanocomposites Download PDFInfo
- Publication number
- AU2005243273B2 AU2005243273B2 AU2005243273A AU2005243273A AU2005243273B2 AU 2005243273 B2 AU2005243273 B2 AU 2005243273B2 AU 2005243273 A AU2005243273 A AU 2005243273A AU 2005243273 A AU2005243273 A AU 2005243273A AU 2005243273 B2 AU2005243273 B2 AU 2005243273B2
- Authority
- AU
- Australia
- Prior art keywords
- polymer
- composition
- phosphonate
- metal
- metal phosphonate
- 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.)
- Ceased
Links
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 161
- 239000002184 metal Substances 0.000 title claims abstract description 161
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 title description 55
- 239000002114 nanocomposite Substances 0.000 title description 8
- 229920000642 polymer Polymers 0.000 claims abstract description 128
- 239000000203 mixture Substances 0.000 claims abstract description 110
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims abstract description 100
- 238000000034 method Methods 0.000 claims abstract description 49
- 230000008569 process Effects 0.000 claims abstract description 44
- 235000013361 beverage Nutrition 0.000 claims abstract description 11
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 57
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 57
- -1 polyethylene terephthalate Polymers 0.000 claims description 35
- 239000011701 zinc Substances 0.000 claims description 28
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 19
- 238000004299 exfoliation Methods 0.000 claims description 19
- 229910052725 zinc Inorganic materials 0.000 claims description 19
- 229920000728 polyester Polymers 0.000 claims description 18
- 239000011575 calcium Substances 0.000 claims description 14
- 238000002156 mixing Methods 0.000 claims description 11
- 239000002243 precursor Substances 0.000 claims description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 10
- 238000006116 polymerization reaction Methods 0.000 claims description 9
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 8
- 229910052791 calcium Inorganic materials 0.000 claims description 8
- 239000011777 magnesium Substances 0.000 claims description 8
- 229920002554 vinyl polymer Polymers 0.000 claims description 8
- 239000004417 polycarbonate Substances 0.000 claims description 7
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 229910052749 magnesium Inorganic materials 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- 229920000098 polyolefin Polymers 0.000 claims description 6
- 238000001746 injection moulding Methods 0.000 claims description 5
- 229910052742 iron Inorganic materials 0.000 claims description 5
- 238000010128 melt processing Methods 0.000 claims description 5
- 229920000515 polycarbonate Polymers 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 4
- 229920002959 polymer blend Polymers 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 3
- 239000010941 cobalt Substances 0.000 claims description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
- 125000000524 functional group Chemical group 0.000 claims description 3
- 229910052746 lanthanum Inorganic materials 0.000 claims description 3
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 229910052684 Cerium Inorganic materials 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
- 238000003801 milling Methods 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 238000002604 ultrasonography Methods 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 4
- 239000004411 aluminium Substances 0.000 claims 2
- 125000003368 amide group Chemical group 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 239000007788 liquid Substances 0.000 claims 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims 1
- 229910052804 chromium Inorganic materials 0.000 claims 1
- 239000011651 chromium Substances 0.000 claims 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims 1
- 230000004888 barrier function Effects 0.000 abstract description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 33
- 239000002245 particle Substances 0.000 description 20
- 239000013078 crystal Substances 0.000 description 17
- 239000000243 solution Substances 0.000 description 17
- 239000010410 layer Substances 0.000 description 15
- 229910052615 phyllosilicate Inorganic materials 0.000 description 14
- 239000000047 product Substances 0.000 description 13
- 238000003756 stirring Methods 0.000 description 12
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 229910021645 metal ion Inorganic materials 0.000 description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
- 230000005484 gravity Effects 0.000 description 8
- 238000011068 loading method Methods 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 230000006872 improvement Effects 0.000 description 7
- 239000011159 matrix material Substances 0.000 description 7
- 239000002086 nanomaterial Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 description 6
- XQKKWWCELHKGKB-UHFFFAOYSA-L calcium acetate monohydrate Chemical compound O.[Ca+2].CC([O-])=O.CC([O-])=O XQKKWWCELHKGKB-UHFFFAOYSA-L 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- NJGCRMAPOWGWMW-UHFFFAOYSA-N octylphosphonic acid Chemical compound CCCCCCCCP(O)(O)=O NJGCRMAPOWGWMW-UHFFFAOYSA-N 0.000 description 5
- YZYKBQUWMPUVEN-UHFFFAOYSA-N zafuleptine Chemical compound OC(=O)CCCCCC(C(C)C)NCC1=CC=C(F)C=C1 YZYKBQUWMPUVEN-UHFFFAOYSA-N 0.000 description 5
- 101000576320 Homo sapiens Max-binding protein MNT Proteins 0.000 description 4
- 229920006121 Polyxylylene adipamide Polymers 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 238000010348 incorporation Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000005411 Van der Waals force Methods 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229920006125 amorphous polymer Polymers 0.000 description 3
- 230000003466 anti-cipated effect Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 239000002178 crystalline material Substances 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 3
- VNFUKGIWLLDPRP-UHFFFAOYSA-J dicalcium;octyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [Ca+2].[Ca+2].CCCCCCCCP([O-])([O-])=O.CCCCCCCCP([O-])([O-])=O VNFUKGIWLLDPRP-UHFFFAOYSA-J 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000012065 filter cake Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 229910052901 montmorillonite Inorganic materials 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 150000003009 phosphonic acids Chemical class 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- DVWGZPGWBGSFPD-UHFFFAOYSA-L zinc;octyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [Zn+2].CCCCCCCCP([O-])([O-])=O DVWGZPGWBGSFPD-UHFFFAOYSA-L 0.000 description 3
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OGBVRMYSNSKIEF-UHFFFAOYSA-N Benzylphosphonic acid Chemical compound OP(O)(=O)CC1=CC=CC=C1 OGBVRMYSNSKIEF-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- ZJDGKLAPAYNDQU-UHFFFAOYSA-J [Zr+4].[O-]P([O-])=O.[O-]P([O-])=O Chemical class [Zr+4].[O-]P([O-])=O.[O-]P([O-])=O ZJDGKLAPAYNDQU-UHFFFAOYSA-J 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000001639 calcium acetate Substances 0.000 description 2
- 229960005147 calcium acetate Drugs 0.000 description 2
- 235000011092 calcium acetate Nutrition 0.000 description 2
- 229940067460 calcium acetate monohydrate Drugs 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- DZQISOJKASMITI-UHFFFAOYSA-N decyl-dioxido-oxo-$l^{5}-phosphane;hydron Chemical compound CCCCCCCCCCP(O)(O)=O DZQISOJKASMITI-UHFFFAOYSA-N 0.000 description 2
- NDPCEEJCYYCUPO-UHFFFAOYSA-J dicalcium;dioxido-oxo-phenyl-$l^{5}-phosphane Chemical compound [Ca+2].[Ca+2].[O-]P([O-])(=O)C1=CC=CC=C1.[O-]P([O-])(=O)C1=CC=CC=C1 NDPCEEJCYYCUPO-UHFFFAOYSA-J 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000004815 dispersion polymer Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 230000037406 food intake Effects 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 239000002667 nucleating agent Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 238000000399 optical microscopy Methods 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- OUZWZJAPXUDCHE-UHFFFAOYSA-L zinc;diacetate;tetrahydrate Chemical compound O.O.O.O.[Zn+2].CC([O-])=O.CC([O-])=O OUZWZJAPXUDCHE-UHFFFAOYSA-L 0.000 description 2
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 1
- ZHJGWYRLJUCMRT-UHFFFAOYSA-N 5-[6-[(4-methylpiperazin-1-yl)methyl]benzimidazol-1-yl]-3-[1-[2-(trifluoromethyl)phenyl]ethoxy]thiophene-2-carboxamide Chemical compound C=1C=CC=C(C(F)(F)F)C=1C(C)OC(=C(S1)C(N)=O)C=C1N(C1=C2)C=NC1=CC=C2CN1CCN(C)CC1 ZHJGWYRLJUCMRT-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229910052776 Thorium Inorganic materials 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- QLZHNIAADXEJJP-UHFFFAOYSA-L dioxido-oxo-phenyl-$l^{5}-phosphane Chemical compound [O-]P([O-])(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-L 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 229940042400 direct acting antivirals phosphonic acid derivative Drugs 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- UFRKOOWSQGXVKV-UHFFFAOYSA-N ethene;ethenol Chemical compound C=C.OC=C UFRKOOWSQGXVKV-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000004715 ethylene vinyl alcohol Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 230000002687 intercalation Effects 0.000 description 1
- 238000009830 intercalation Methods 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 229940097364 magnesium acetate tetrahydrate Drugs 0.000 description 1
- XKPKPGCRSHFTKM-UHFFFAOYSA-L magnesium;diacetate;tetrahydrate Chemical compound O.O.O.O.[Mg+2].CC([O-])=O.CC([O-])=O XKPKPGCRSHFTKM-UHFFFAOYSA-L 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 239000002071 nanotube Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000003007 phosphonic acid derivatives Chemical class 0.000 description 1
- 229920006112 polar polymer Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 0.000 description 1
- 238000002525 ultrasonication Methods 0.000 description 1
- DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3834—Aromatic acids (P-C aromatic linkage)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3882—Arylalkanephosphonic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
-
- 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
- C08K5/0091—Complexes with metal-heteroatom-bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2
-
- 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
- C08K7/00—Use of ingredients characterised by shape
-
- 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
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Containers Having Bodies Formed In One Piece (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Laminated Bodies (AREA)
- Wrappers (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
- Superconductors And Manufacturing Methods Therefor (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56415004P | 2004-04-21 | 2004-04-21 | |
| US60/564,150 | 2004-04-21 | ||
| PCT/US2005/013612 WO2005111131A2 (en) | 2004-04-21 | 2005-04-21 | Metal phosphonates and related nanocomposites |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2005243273A1 AU2005243273A1 (en) | 2005-11-24 |
| AU2005243273B2 true AU2005243273B2 (en) | 2010-03-04 |
Family
ID=35394731
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2005243273A Ceased AU2005243273B2 (en) | 2004-04-21 | 2005-04-21 | Metal phosphonates and related nanocomposites |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7199172B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1742992B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2007534801A (cg-RX-API-DMAC7.html) |
| AT (1) | ATE521662T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU2005243273B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BRPI0510101A (cg-RX-API-DMAC7.html) |
| CA (1) | CA2564554A1 (cg-RX-API-DMAC7.html) |
| MX (1) | MXPA06012199A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2005111131A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006012581A2 (en) * | 2004-07-23 | 2006-02-02 | University Of South Carolina | Polymer composite materials and methods for producing the same |
| US7163977B2 (en) * | 2005-05-13 | 2007-01-16 | Plastic Technologies, Inc. | Method to reduce the aldehyde content of polymers |
| JP5187476B2 (ja) * | 2006-03-13 | 2013-04-24 | 石原薬品株式会社 | ナノコンポジット |
| US7989115B2 (en) * | 2007-12-14 | 2011-08-02 | Gore Enterprise Holdings, Inc. | Highly stable fuel cell membranes and methods of making them |
| WO2010082643A1 (ja) * | 2009-01-16 | 2010-07-22 | 帝人ファイバー株式会社 | ポリエステル繊維およびその製造方法、並びにそのポリエステル繊維を含むタイヤコード、タイヤ、ベルト補強用繊維材料およびベルト |
| JP4897021B2 (ja) * | 2009-09-07 | 2012-03-14 | 帝人ファイバー株式会社 | ベルト補強用繊維材料及びそれを用いてなるベルト |
| JP4634526B1 (ja) * | 2009-01-16 | 2011-02-16 | 帝人ファイバー株式会社 | ポリエステル繊維及びその製造方法 |
| JP4897020B2 (ja) * | 2009-09-07 | 2012-03-14 | 帝人ファイバー株式会社 | タイヤコード及びそれを用いてなるタイヤ |
| CN102414266B (zh) | 2009-04-30 | 2015-12-09 | 美利肯公司 | 成核剂和包含该成核剂的热塑性组合物 |
| JP2011058105A (ja) * | 2009-09-07 | 2011-03-24 | Teijin Fibers Ltd | ホース補強用繊維コード及びホース |
| KR101763646B1 (ko) * | 2009-09-09 | 2017-08-01 | 닛산 가가쿠 고교 가부시키 가이샤 | 포스폰산 금속염의 제조방법 및 포스폰산 금속염을 포함하는 열가소성 수지 조성물 |
| JP5910815B2 (ja) * | 2011-12-27 | 2016-04-27 | 日産化学工業株式会社 | フェニルホスホン酸金属塩を含有する樹脂組成物 |
| JP6225601B2 (ja) * | 2013-09-24 | 2017-11-08 | Dic株式会社 | 水蒸気バリア接着剤用樹脂組成物の製造方法、および水蒸気バリア用接着剤、水蒸気バリア用フィルム、水蒸気バリア用コーティング剤、水蒸気バリア用積層体 |
| WO2017160528A1 (en) | 2016-03-15 | 2017-09-21 | Colormatrix Holdings, Inc. | Barrier additives |
| CN109265743B (zh) * | 2018-09-07 | 2020-03-17 | 中国科学院宁波材料技术与工程研究所 | 阻燃剂、复合阻燃剂以及含有该复合阻燃剂的阻燃高分子材料 |
| CA3214017A1 (en) | 2021-04-22 | 2022-10-27 | Darin Dotson | Polyethylene polymer compositions and articles made from the same |
| EP4326811A1 (en) * | 2021-04-22 | 2024-02-28 | Milliken & Company | Polypropylene polymer compositions and articles made from the same |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3488368A (en) * | 1967-01-30 | 1970-01-06 | Geigy Chem Corp | Metal derivatives of alkylhydroxyphenylalkylphosphinic acids |
| US5558517A (en) * | 1992-02-24 | 1996-09-24 | Clemson University | Polymeric prosthesis having a phosphonylated surface |
| WO2003081691A2 (en) * | 2002-03-22 | 2003-10-02 | Fuma-Tech Gesellschaft Für Funktionelle Membranen Und Anlagetechnologie Mbh | An innovative method for the preparation of proton conducting nanopolymeric membranes for use in fuel cells or in catalytic membrane reactors |
Family Cites Families (74)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2579810A (en) | 1949-08-18 | 1951-12-25 | Research Corp | Process of preparing substituted hydroxymethylphosphonic esters |
| US3014949A (en) * | 1958-09-26 | 1961-12-26 | Monsanto Chemicals | Oxo phosphates, phosphonates and phosphinates |
| JPS4874550A (cg-RX-API-DMAC7.html) | 1972-01-08 | 1973-10-08 | ||
| US4263425A (en) * | 1977-08-10 | 1981-04-21 | Zimmer Aktiengesellschaft | Process for production of polyester polymer for food packing |
| US4291111A (en) * | 1977-11-25 | 1981-09-22 | Xerox Corporation | Nitrogen-containing additives for magnetic toners having hydrophobic and hydrophilic moiety |
| US4446041A (en) * | 1978-04-10 | 1984-05-01 | Neary Michael P | Solar energy system |
| US4224203A (en) * | 1978-09-05 | 1980-09-23 | Argus Chemical Corporation | Vinyl chloride polymer stabilizer comprising a metal organophosphonate |
| US4374242A (en) * | 1979-07-24 | 1983-02-15 | Occidental Research Corporation | Layered organoarsenous inorganic polymers |
| US4276411A (en) * | 1979-07-24 | 1981-06-30 | Occidental Research Corporation | Layered organophosphorus inorganic polymers containing acyclic groups |
| US4232146A (en) * | 1978-09-26 | 1980-11-04 | Occidental Research Corporation | Process for preparing layered organophosphorus inorganic polymers |
| US4436899A (en) * | 1978-09-26 | 1984-03-13 | Occidental Research Corporation | Layered organophosphorus inorganic polymers |
| US4256872A (en) * | 1978-09-26 | 1981-03-17 | Occidental Research Corporation | Process for preparing layered organophosphorus inorganic polymers |
| US4267308A (en) * | 1979-01-29 | 1981-05-12 | Occidental Research Corporation | Layered zirconium bis(benzenephosphonate) inorganic polymers |
| US4291093A (en) * | 1979-10-05 | 1981-09-22 | Phillips Petroleum Co. | Stabilized polyolefin substrate overcoated with an ethoxylated lubricant and a phosphate ester |
| US4260542A (en) * | 1979-10-25 | 1981-04-07 | Monsanto Company | Reaction products of metal oxides and salts with phosphorus compounds |
| US4446061A (en) | 1979-10-25 | 1984-05-01 | Monsanto Company | Composition containing reaction products of metal oxides and salts with phosphorus compounds |
| FR2502162B1 (fr) | 1981-03-20 | 1985-10-04 | Rhone Poulenc Spec Chim | Compositions a mouler a base de polyesthers thermoplastiques |
| JPS57195143A (en) * | 1981-05-27 | 1982-11-30 | Teijin Ltd | Polyester composition |
| JPS58101021A (ja) * | 1981-12-12 | 1983-06-16 | Toyobo Co Ltd | ２軸延伸ポリエステルフイルム |
| US4409375A (en) * | 1982-02-11 | 1983-10-11 | Champion International Corporation | Method for scavenging aldehydes |
| MTP932B (en) * | 1982-06-01 | 1986-12-10 | Int Paint Plc | Anti-corrosive point |
| US4591629A (en) * | 1983-04-21 | 1986-05-27 | Ems-Inventa Ag | Process for the purification of high molecular weight polyesters |
| US4883892A (en) * | 1985-05-23 | 1989-11-28 | Akzo America Inc. | Phosphate and phosphonate compounds |
| US5234979A (en) * | 1985-06-29 | 1993-08-10 | Toedtemann Gert | Thermoplastic mounding compositions with flame-repellant properties |
| US4759971A (en) * | 1985-10-07 | 1988-07-26 | Occidental Research Corporation | Multilayered structure |
| GB8611357D0 (en) * | 1986-05-09 | 1986-06-18 | Ciba Geigy Ag | Flame retardent polymer compositions |
| US4837115A (en) | 1986-07-30 | 1989-06-06 | Toyo Seikan Kaisha, Ltd. | Thermoplastic polyester composition having improved flavor-retaining property and vessel formed therefrom |
| US4962228A (en) * | 1987-03-09 | 1990-10-09 | Mobil Oil Corporation | Layered divalent metal phosphates containing pendent substituent groups and their preparation |
| IT1243781B (it) * | 1990-08-03 | 1994-06-28 | Eniricerche Spa | Composizione solida cristallina mesoporosa di difosfonato-fosfito di un metallo tetravalente, con una stretta distribuzione di mesopori |
| IT1244485B (it) * | 1990-12-21 | 1994-07-15 | Eniricerche Spa | Composizione solida cristallina microporosa di difosfonato-fosfito di un metallo tetravalente con una stretta distribuzione di micropori |
| DE69214686T2 (de) * | 1991-02-28 | 1997-06-05 | Agfa Gevaert Nv | Verfahren zur Herstellung von Polyestern mit verbesserter thermooxydativer Stabilität |
| US5258233A (en) | 1992-04-02 | 1993-11-02 | Eastman Kodak Company | Polyester/polyamide blend having improved flavor retaining property and clarity |
| US5310771A (en) * | 1992-04-23 | 1994-05-10 | Phillips Petroleum Company | Polyolefin stabilization |
| CA2139061C (en) * | 1993-12-28 | 1998-12-08 | Mitsui Chemicals, Inc. | Process for preparing polyester |
| DE4400300A1 (de) * | 1994-01-07 | 1995-07-13 | Akzo Nobel Nv | Verfahren zur Herstellung von film- und faserbildenden Polyestern und Copolyestern |
| US5616749A (en) * | 1994-09-27 | 1997-04-01 | National Science Council | Preparation of layered zirconium phosphite sulfophenylphosphonates and their use as a catalyst |
| US5608032A (en) * | 1995-03-28 | 1997-03-04 | Industrial Technology Research Institute | Catalytic compositions for the proparation of poly(ethylene terephthalate) with attenuated yellow color |
| DE19518943C2 (de) * | 1995-05-23 | 1999-12-09 | Inventa Fischer Gmbh | Verfahren zur Herstellung von Polyestern unter Verwendung von titanhaltigen Katalysator-Inhibitor-Kombinationen |
| US5844032A (en) * | 1995-06-07 | 1998-12-01 | Amcol International Corporation | Intercalates and exfoliates formed with non-EVOH monomers, oligomers and polymers; and EVOH composite materials containing same |
| US5519108A (en) * | 1995-06-07 | 1996-05-21 | Industrial Technology Research Institute | Catalytic compositions containing tetrabutyl titanate and a mixture of cocatalysts for the preparation of poly(butylene terephthalate) |
| US6228903B1 (en) * | 1995-06-07 | 2001-05-08 | Amcol International Corporation | Exfoliated layered materials and nanocomposites comprising said exfoliated layered materials having water-insoluble oligomers or polymers adhered thereto |
| US5721306A (en) * | 1995-06-07 | 1998-02-24 | Amcol International Corporation | Viscous carrier compositions, including gels, formed with an organic liquid carrier and a layered material:polymer complex |
| US5760121A (en) * | 1995-06-07 | 1998-06-02 | Amcol International Corporation | Intercalates and exfoliates formed with oligomers and polymers and composite materials containing same |
| US5650469A (en) | 1995-10-25 | 1997-07-22 | Eastman Chemical Company | Polyester/polyamide blend having improved flavor retaining property and clarity |
| TW336248B (en) | 1996-02-05 | 1998-07-11 | Eastman Kodak Co | Polyester/polyesteramide blends the invention relates to polyester/polyesteramide blends |
| DE19608006A1 (de) * | 1996-03-04 | 1997-09-11 | Hoechst Ag | Salze von phosphonigen Säuren und deren Verwendung als Flammschutzmittel in Kunststoffen |
| EP0893475B1 (en) * | 1996-04-08 | 2003-07-30 | Kaneka Corporation | Flame retardant plastic resin composition |
| DE19614424A1 (de) * | 1996-04-12 | 1997-10-16 | Hoechst Ag | Synergistische Flammschutzmittel-Kombination für Polymere |
| US5898058A (en) * | 1996-05-20 | 1999-04-27 | Wellman, Inc. | Method of post-polymerization stabilization of high activity catalysts in continuous polyethylene terephthalate production |
| US6042908A (en) | 1996-08-22 | 2000-03-28 | Eastman Chemical Company | Process for improving the flavor retaining property of polyester/polyamide blend containers for ozonated water |
| US6395865B2 (en) * | 1997-12-05 | 2002-05-28 | Continental Pet Technologies Inc | Process for making pen/pet blends and transparent articles therefrom |
| US5902539A (en) * | 1996-12-06 | 1999-05-11 | Continental Pet Technologies, Inc. | Process for making PEN/PET blends and transparent articles therefrom |
| US5830992A (en) * | 1996-12-12 | 1998-11-03 | Union Camp Corporation | Light color, color stable rosin esters and methods for preparing same |
| NL1008003C2 (nl) * | 1998-01-09 | 1999-07-12 | Tno | Nanocomposiet-materiaal. |
| DE19820399A1 (de) * | 1998-05-07 | 1999-11-11 | Basf Ag | Flammgeschützte Polyesterformmassen |
| US6239233B1 (en) | 1998-10-09 | 2001-05-29 | Eastman Chemical Company | Polyester/polyamide blends with improved color |
| ID27680A (id) * | 1998-10-26 | 2001-04-19 | Toray Industries | Komposisi poliester, metoda produksi daripadanya dan film poliester |
| US6043335A (en) * | 1999-10-04 | 2000-03-28 | General Electric Company | Phosphate-containing catalyst composition for the preparation of polyesters, and related processes |
| US6274212B1 (en) | 2000-02-22 | 2001-08-14 | The Coca-Cola Company | Method to decrease the acetaldehyde content of melt-processed polyesters |
| US7056963B2 (en) * | 2000-05-19 | 2006-06-06 | Kaneka Corporation | Polyester resin composition and process for the preparation thereof |
| AU769207B2 (en) * | 2000-08-22 | 2004-01-22 | Mitsui Chemicals, Inc. | Catalysts for polyester production, process for producing polyester, and polyester |
| DE10045719B4 (de) * | 2000-09-15 | 2018-01-11 | Inventa-Fischer Gmbh & Co. Kg | Verfahren zur Herstellung von Polyestern mit reduziertem Gehalt an Acetaldehyd |
| CA2364520C (en) * | 2000-12-08 | 2010-04-20 | Toyo Seikan Kaisha, Ltd. | Packaging material and multi-layer container |
| TWI288155B (en) * | 2001-01-12 | 2007-10-11 | Nanya Plastics Corp | Manufacturing method of copolyester for PET bottles comprising low acetaldehyde content |
| WO2002059178A1 (en) * | 2001-01-25 | 2002-08-01 | Mitsubishi Chemical Corporation | Polyester resin, molded article thereof, and process for producing polyester resin |
| JP4393004B2 (ja) * | 2001-02-06 | 2010-01-06 | 三菱化学株式会社 | ポリエステル樹脂 |
| US6489433B2 (en) * | 2001-02-23 | 2002-12-03 | E. I. Du Pont De Nemours And Company | Metal-containing composition and process therewith |
| US6506853B2 (en) * | 2001-02-28 | 2003-01-14 | E. I. Du Pont De Nemours And Company | Copolymer comprising isophthalic acid |
| DE10132058A1 (de) | 2001-07-05 | 2003-01-16 | Basf Ag | Flammgeschützte thermoplastische Formmassen |
| US6774204B1 (en) * | 2001-09-26 | 2004-08-10 | E. I. Du Pont De Nemours And Company | Polyester and process therefor |
| US7273899B2 (en) * | 2002-09-25 | 2007-09-25 | Eastman Kodak Company | Materials and method for making splayed layered materials |
| US7189777B2 (en) * | 2003-06-09 | 2007-03-13 | Eastman Chemical Company | Compositions and method for improving reheat rate of PET using activated carbon |
| US6911523B2 (en) | 2003-07-17 | 2005-06-28 | Colormatrix Corporation | Method to decrease the aldehyde content of polyesters |
| US7101923B2 (en) * | 2003-10-03 | 2006-09-05 | General Electric Company | Flame-retardant thermoset composition, method, and article |
-
2005
- 2005-04-20 US US11/110,269 patent/US7199172B2/en not_active Expired - Fee Related
- 2005-04-21 BR BRPI0510101-8A patent/BRPI0510101A/pt not_active IP Right Cessation
- 2005-04-21 WO PCT/US2005/013612 patent/WO2005111131A2/en not_active Ceased
- 2005-04-21 EP EP05779066A patent/EP1742992B1/en not_active Expired - Lifetime
- 2005-04-21 JP JP2007509629A patent/JP2007534801A/ja active Pending
- 2005-04-21 AU AU2005243273A patent/AU2005243273B2/en not_active Ceased
- 2005-04-21 AT AT05779066T patent/ATE521662T1/de not_active IP Right Cessation
- 2005-04-21 MX MXPA06012199A patent/MXPA06012199A/es active IP Right Grant
- 2005-04-21 CA CA002564554A patent/CA2564554A1/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3488368A (en) * | 1967-01-30 | 1970-01-06 | Geigy Chem Corp | Metal derivatives of alkylhydroxyphenylalkylphosphinic acids |
| US5558517A (en) * | 1992-02-24 | 1996-09-24 | Clemson University | Polymeric prosthesis having a phosphonylated surface |
| WO2003081691A2 (en) * | 2002-03-22 | 2003-10-02 | Fuma-Tech Gesellschaft Für Funktionelle Membranen Und Anlagetechnologie Mbh | An innovative method for the preparation of proton conducting nanopolymeric membranes for use in fuel cells or in catalytic membrane reactors |
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA06012199A (es) | 2007-01-17 |
| JP2007534801A (ja) | 2007-11-29 |
| AU2005243273A1 (en) | 2005-11-24 |
| US20050239938A1 (en) | 2005-10-27 |
| CA2564554A1 (en) | 2005-11-24 |
| WO2005111131A3 (en) | 2006-05-04 |
| US7199172B2 (en) | 2007-04-03 |
| ATE521662T1 (de) | 2011-09-15 |
| BRPI0510101A (pt) | 2007-09-25 |
| EP1742992A2 (en) | 2007-01-17 |
| WO2005111131A2 (en) | 2005-11-24 |
| EP1742992A4 (en) | 2009-09-23 |
| WO2005111131B1 (en) | 2006-06-22 |
| EP1742992B1 (en) | 2011-08-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2005243273B2 (en) | Metal phosphonates and related nanocomposites | |
| US6828370B2 (en) | Intercalates and exfoliates thereof having an improved level of extractable material | |
| AU758550B2 (en) | A high barrier amorphous polyamide-clay nanocomposite and a process for preparing same | |
| US6737464B1 (en) | Polymer nanocomposite comprising a matrix polymer and a layered clay material having a low quartz content | |
| EP1141136B1 (en) | A polymer/clay nanocomposite comprising a functionalized polymer or oligomer and a process for preparing same | |
| US20020119266A1 (en) | Polymer-clay nanocomposite comprising an amorphous oligomer | |
| WO2000078540A9 (en) | High performance nanocomposites | |
| CN111065671B (zh) | 阻隔添加剂 | |
| JP2006524732A (ja) | ナノメートル成層化合物を含む熱可塑性材料 | |
| US7786189B2 (en) | Oligomer-modified layered inorganic compounds and their use in nanocomposites | |
| AU771071B2 (en) | A polymer/clay nanocomposite comprising a clay mixture and a process for making same | |
| US7951860B2 (en) | Polymer composite materials and methods for producing the same | |
| WO2016209165A1 (en) | A modified layered clay material and composites containing the same | |
| Moloney | Development of masterbatches for poly (ethylene terephthalate) with improved resistance to CO2 permeation | |
| Shibata | Mechanisms of biodegradability generation in polymer nanocomposites |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) | ||
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |