RU2414479C2 - Бромированные бутадиен/винилароматические сополимеры, смеси таких сополимеров с винилароматическим полимером и полимерные пеноматериалы, полученные из таких смесей - Google Patents
Бромированные бутадиен/винилароматические сополимеры, смеси таких сополимеров с винилароматическим полимером и полимерные пеноматериалы, полученные из таких смесей Download PDFInfo
- Publication number
- RU2414479C2 RU2414479C2 RU2008123837/04A RU2008123837A RU2414479C2 RU 2414479 C2 RU2414479 C2 RU 2414479C2 RU 2008123837/04 A RU2008123837/04 A RU 2008123837/04A RU 2008123837 A RU2008123837 A RU 2008123837A RU 2414479 C2 RU2414479 C2 RU 2414479C2
- Authority
- RU
- Russia
- Prior art keywords
- copolymer
- butadiene
- brominated
- weight
- styrene
- Prior art date
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- 229920001577 copolymer Polymers 0.000 title claims abstract description 155
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 title claims abstract description 90
- 229920000642 polymer Polymers 0.000 title claims abstract description 73
- 239000000203 mixture Substances 0.000 title claims description 66
- 239000000463 material Substances 0.000 title description 13
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 56
- 238000000034 method Methods 0.000 claims abstract description 50
- 239000000654 additive Substances 0.000 claims abstract description 24
- 239000003063 flame retardant Substances 0.000 claims abstract description 23
- 239000000178 monomer Substances 0.000 claims abstract description 23
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims abstract description 21
- 238000002411 thermogravimetry Methods 0.000 claims abstract description 18
- 230000000996 additive effect Effects 0.000 claims abstract description 13
- 229920002959 polymer blend Polymers 0.000 claims abstract description 13
- 239000012634 fragment Substances 0.000 claims abstract description 11
- 238000005160 1H NMR spectroscopy Methods 0.000 claims abstract description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 75
- 238000005893 bromination reaction Methods 0.000 claims description 68
- 230000031709 bromination Effects 0.000 claims description 66
- 239000006260 foam Substances 0.000 claims description 64
- 229910052794 bromium Inorganic materials 0.000 claims description 58
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 57
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 49
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 47
- 239000008187 granular material Substances 0.000 claims description 33
- 239000002904 solvent Substances 0.000 claims description 23
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 23
- 239000004793 Polystyrene Substances 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 21
- 229920002223 polystyrene Polymers 0.000 claims description 20
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 20
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical group Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 17
- 229920001400 block copolymer Polymers 0.000 claims description 16
- 239000004088 foaming agent Substances 0.000 claims description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- JQRYUMGHOUYJFW-UHFFFAOYSA-N pyridine;trihydrobromide Chemical compound [Br-].[Br-].[Br-].C1=CC=[NH+]C=C1.C1=CC=[NH+]C=C1.C1=CC=[NH+]C=C1 JQRYUMGHOUYJFW-UHFFFAOYSA-N 0.000 claims description 12
- 230000004580 weight loss Effects 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 10
- -1 alkyl styrenes Chemical class 0.000 claims description 8
- 150000003440 styrenes Chemical class 0.000 claims description 8
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 claims description 6
- QNRMTGGDHLBXQZ-UHFFFAOYSA-N buta-1,2-diene Chemical class CC=C=C QNRMTGGDHLBXQZ-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 4
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 4
- 229920005604 random copolymer Polymers 0.000 claims description 4
- WGGLDBIZIQMEGH-UHFFFAOYSA-N 1-bromo-4-ethenylbenzene Chemical compound BrC1=CC=C(C=C)C=C1 WGGLDBIZIQMEGH-UHFFFAOYSA-N 0.000 claims description 3
- OEVVKKAVYQFQNV-UHFFFAOYSA-N 1-ethenyl-2,4-dimethylbenzene Chemical compound CC1=CC=C(C=C)C(C)=C1 OEVVKKAVYQFQNV-UHFFFAOYSA-N 0.000 claims description 3
- VKVLTUQLNXVANB-UHFFFAOYSA-N 1-ethenyl-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1C=C VKVLTUQLNXVANB-UHFFFAOYSA-N 0.000 claims description 3
- YFZHODLXYNDBSM-UHFFFAOYSA-N 1-ethenyl-4-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(C=C)C=C1 YFZHODLXYNDBSM-UHFFFAOYSA-N 0.000 claims description 3
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 3
- UAJRSHJHFRVGMG-UHFFFAOYSA-N 1-ethenyl-4-methoxybenzene Chemical compound COC1=CC=C(C=C)C=C1 UAJRSHJHFRVGMG-UHFFFAOYSA-N 0.000 claims description 2
- 239000012963 UV stabilizer Substances 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 125000003158 alcohol group Chemical group 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 2
- BXOUVIIITJXIKB-UHFFFAOYSA-N ethene;styrene Chemical compound C=C.C=CC1=CC=CC=C1 BXOUVIIITJXIKB-UHFFFAOYSA-N 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000002667 nucleating agent Substances 0.000 claims description 2
- 229920003251 poly(α-methylstyrene) Polymers 0.000 claims description 2
- 239000003017 thermal stabilizer Substances 0.000 claims description 2
- SSZOCHFYWWVSAI-UHFFFAOYSA-N 1-bromo-2-ethenylbenzene Chemical compound BrC1=CC=CC=C1C=C SSZOCHFYWWVSAI-UHFFFAOYSA-N 0.000 claims 2
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 claims 2
- 230000001413 cellular effect Effects 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- SFBTTWXNCQVIEC-UHFFFAOYSA-N o-Vinylanisole Chemical compound COC1=CC=CC=C1C=C SFBTTWXNCQVIEC-UHFFFAOYSA-N 0.000 claims 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- 239000000370 acceptor Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 9
- 230000000694 effects Effects 0.000 abstract description 5
- 208000020442 loss of weight Diseases 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 61
- 239000005062 Polybutadiene Substances 0.000 description 41
- 229920002857 polybutadiene Polymers 0.000 description 41
- 239000000243 solution Substances 0.000 description 41
- 238000012360 testing method Methods 0.000 description 33
- DEIGXXQKDWULML-UHFFFAOYSA-N 1,2,5,6,9,10-hexabromocyclododecane Chemical compound BrC1CCC(Br)C(Br)CCC(Br)C(Br)CCC1Br DEIGXXQKDWULML-UHFFFAOYSA-N 0.000 description 23
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 239000000047 product Substances 0.000 description 21
- 239000011347 resin Substances 0.000 description 18
- 229920005989 resin Polymers 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 238000006116 polymerization reaction Methods 0.000 description 16
- IYSTUUQQVNNJDN-UHFFFAOYSA-N 2-[4-(4,5-diphenyl-1H-imidazol-2-yl)phenyl]-1H-imidazo[4,5-f][1,10]phenanthroline Chemical compound C1(=CC=CC=C1)C=1N=C(NC=1C1=CC=CC=C1)C1=CC=C(C=C1)C=1NC=2C(=C3C=CC=NC3=C3N=CC=CC=23)N=1 IYSTUUQQVNNJDN-UHFFFAOYSA-N 0.000 description 15
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 14
- 238000001125 extrusion Methods 0.000 description 14
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 12
- 238000002156 mixing Methods 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 11
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 11
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 10
- GPWHDDKQSYOYBF-UHFFFAOYSA-N ac1l2u0q Chemical compound Br[Br-]Br GPWHDDKQSYOYBF-UHFFFAOYSA-N 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 10
- 239000003381 stabilizer Substances 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 125000005207 tetraalkylammonium group Chemical group 0.000 description 10
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 10
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- 239000011541 reaction mixture Substances 0.000 description 9
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 8
- 125000001246 bromo group Chemical group Br* 0.000 description 8
- 239000000499 gel Substances 0.000 description 8
- 229920001519 homopolymer Polymers 0.000 description 8
- 239000003999 initiator Substances 0.000 description 8
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 8
- 229910002092 carbon dioxide Inorganic materials 0.000 description 7
- 238000001914 filtration Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000003607 modifier Substances 0.000 description 7
- 150000003254 radicals Chemical class 0.000 description 7
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 6
- 238000005481 NMR spectroscopy Methods 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 6
- 239000001569 carbon dioxide Substances 0.000 description 6
- 230000008859 change Effects 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 238000005187 foaming Methods 0.000 description 6
- 238000005227 gel permeation chromatography Methods 0.000 description 6
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 6
- 230000002285 radioactive effect Effects 0.000 description 6
- 229920003048 styrene butadiene rubber Polymers 0.000 description 6
- 230000002411 adverse Effects 0.000 description 5
- 150000001649 bromium compounds Chemical group 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 5
- 230000007246 mechanism Effects 0.000 description 5
- 239000012074 organic phase Substances 0.000 description 5
- 238000001556 precipitation Methods 0.000 description 5
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000001282 iso-butane Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 3
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000007942 carboxylates Chemical class 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 150000001993 dienes Chemical class 0.000 description 3
- 229920006248 expandable polystyrene Polymers 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 230000000977 initiatory effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- BBFCIBZLAVOLCF-UHFFFAOYSA-N pyridin-1-ium;bromide Chemical compound Br.C1=CC=NC=C1 BBFCIBZLAVOLCF-UHFFFAOYSA-N 0.000 description 3
- 238000010791 quenching Methods 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- 230000033228 biological regulation Effects 0.000 description 2
- 238000000071 blow moulding Methods 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical class C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000004795 extruded polystyrene foam Substances 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000003456 ion exchange resin Substances 0.000 description 2
- 229920003303 ion-exchange polymer Polymers 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 238000007347 radical substitution reaction Methods 0.000 description 2
- 239000012047 saturated solution Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- SFLXUZPXEWWQNH-UHFFFAOYSA-K tetrabutylazanium;tribromide Chemical compound [Br-].[Br-].[Br-].CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC SFLXUZPXEWWQNH-UHFFFAOYSA-K 0.000 description 2
- PRXNKYBFWAWBNZ-UHFFFAOYSA-N trimethylphenylammonium tribromide Chemical compound Br[Br-]Br.C[N+](C)(C)C1=CC=CC=C1 PRXNKYBFWAWBNZ-UHFFFAOYSA-N 0.000 description 2
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- SPPWGCYEYAMHDT-UHFFFAOYSA-N 1,4-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=C(C(C)C)C=C1 SPPWGCYEYAMHDT-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- AWFYPPSBLUWMFQ-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(1,4,6,7-tetrahydropyrazolo[4,3-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=C2 AWFYPPSBLUWMFQ-UHFFFAOYSA-N 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000002879 Lewis base Substances 0.000 description 1
- 241000208202 Linaceae Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 241000392928 Parachromis friedrichsthalii Species 0.000 description 1
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Classifications
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/18—Introducing halogen atoms or halogen-containing groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/12—Incorporating halogen atoms into the molecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F236/10—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated with vinyl-aromatic monomers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F236/14—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen
- C08F236/16—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen containing halogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/18—Introducing halogen atoms or halogen-containing groups
- C08F8/20—Halogenation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/16—Making expandable particles
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2325/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
- C08J2325/02—Homopolymers or copolymers of hydrocarbons
- C08J2325/04—Homopolymers or copolymers of styrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2453/00—Characterised by the use of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
Landscapes
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
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| US73536105P | 2005-11-12 | 2005-11-12 | |
| US60/735,361 | 2005-11-12 |
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| EP (1) | EP1957544B1 (enExample) |
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| DE (1) | DE602006011944D1 (enExample) |
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| NO (1) | NO20081960L (enExample) |
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| WO2020139110A1 (en) | 2018-12-27 | 2020-07-02 | Public Joint Stock Company "Sibur Holding" | Modified (co)polymer, method for preparing thereof and use of the same |
| WO2020139112A1 (en) | 2018-12-27 | 2020-07-02 | Public Joint Stock Company "Sibur Holding" | Modified diene-containing (co)polymer, method for preparing thereof and use as a flame retardant |
| WO2020139114A1 (en) | 2018-12-27 | 2020-07-02 | Public Joint Stock Company "Sibur Holding" | Modified diene-containing (co)polymer, method for preparing thereof and use of the same as flame retardant |
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| RU2794096C2 (ru) * | 2018-12-27 | 2023-04-11 | Публичное акционерное общество "СИБУР Холдинг" | Модифицированный диенсодержащий (cо)полимер, способ его получения и применение в качестве антипирена |
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| EP2789651A1 (de) | 2013-04-11 | 2014-10-15 | Basf Se | Flammschutzmittelzusammensetzung zur Verwendung in Styrolpolymerschaumstoffen |
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| JP6541555B2 (ja) * | 2015-11-25 | 2019-07-10 | 株式会社ジェイエスピー | ポリスチレン系樹脂発泡板の製造方法 |
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| IT201600071347A1 (it) | 2016-07-08 | 2018-01-08 | Versalis Spa | Composizioni espandibili contenenti polimeri vinil aromatici aventi proprietà autoestinguenti e migliorata processabilità |
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| CA3042237A1 (en) | 2016-11-02 | 2018-05-11 | Dow Global Technologies Llc | Semi-crystalline polyolefin-based additive masterbatch composition |
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| EP3625310B1 (de) | 2017-05-17 | 2021-04-28 | Basf Se | Bromierte flammschutzmittel |
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| JP6335368B2 (ja) * | 2017-06-13 | 2018-05-30 | 株式会社ジェイエスピー | ポリスチレン系樹脂押出発泡板の製造方法 |
| JP6366149B2 (ja) * | 2017-06-13 | 2018-08-01 | 株式会社ジェイエスピー | ポリスチレン系樹脂押出発泡板 |
| CN110997777B (zh) | 2017-08-04 | 2022-08-02 | 株式会社钟化 | 发泡性聚苯乙烯系树脂颗粒、聚苯乙烯系预发泡颗粒、发泡成型体、及它们的制造方法 |
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| CN108129618B (zh) * | 2017-12-12 | 2019-10-22 | 浙江大学 | 中低分子量含溴多嵌段共聚物阻燃剂及其溶液三步制备法 |
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Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1301497B (de) * | 1966-01-05 | 1969-08-21 | Basf Ag | Verfahren zur Herstellung bromierter Polymerisate des Butadiens |
| GB1474536A (en) * | 1973-07-30 | 1977-05-25 | Shell Int Research | Halogenated partially hydrogenated block copolymer and its preparation |
| SU597687A1 (ru) * | 1976-03-09 | 1978-03-15 | Предприятие П/Я В-2756 | Бромированный бутадиен-нитрильный каучук как огнестойка добавка в полимерных композици х |
| DD137308A3 (de) * | 1969-09-24 | 1979-08-29 | Paul Herte | Verfahren zur herstellung von bromierten ungesaettigten niedermolekularen polymeren |
| US5532322A (en) * | 1995-09-26 | 1996-07-02 | Manac Inc. | Process for preparing brominated polystyrene |
| RU2177952C2 (ru) * | 1999-03-23 | 2002-01-10 | Щербань Георгий Трофимович | Способ получения галоидированного бутилкаучука |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1075103B (de) | 1960-02-11 | VEB Leuna-Werke "Walter Ulbricht", Leuna (Kr. Merseburg) | Verfahren zur kontinuierlichen Herstellung von Epichlorhydrin aus Glyzerin | |
| DE1260138B (de) | 1966-01-05 | 1968-02-01 | Basf Ag | Formmassen zur Herstellung selbstverloeschender Formkoerper |
| DE1769320A1 (de) | 1968-05-08 | 1971-09-16 | Hoechst Ag | Selbstverloeschende Styrolpolymerisate mit gleichmaessiger Porenstruktur |
| US3668155A (en) * | 1968-06-27 | 1972-06-06 | Dow Chemical Co | Self-extinguishing ethylene copolymer foams comprising a ternary mixture of an antimony compound, a halogen-containing compound and a bromine compound |
| US3639304A (en) * | 1968-06-27 | 1972-02-01 | Dow Chemical Co | Self-extinguishing polyethylene foams comprising an antimony compound a halogen-containing aliphatic or cyclo-aliphatic compound and a bromine-containing aromatic or acyclic compound |
| US3652494A (en) * | 1968-08-16 | 1972-03-28 | Phillips Petroleum Co | Stabilized flameproofed thermoplastic compositions |
| GB1277736A (en) * | 1968-09-30 | 1972-06-14 | British Petroleum Co | Catalyst support |
| US3640941A (en) * | 1970-05-08 | 1972-02-08 | Whittaker Corp | Adhesive composition |
| DE2314544A1 (de) * | 1973-03-23 | 1974-10-10 | Basf Ag | Feinteilige, expandierbare, schwer entflammbare styrolpolymerisate mit guter verarbeitbarkeit |
| JPS5125592A (en) * | 1974-08-27 | 1976-03-02 | Toray Industries | Shusokajugotaino seizohoho |
| JPS5424997A (en) * | 1977-07-27 | 1979-02-24 | Tokai Rubber Ind Ltd | Chlorinated brominated elastmer of styreneebutadiene copolymer |
| JPS55135101A (en) * | 1979-04-11 | 1980-10-21 | Japan Synthetic Rubber Co Ltd | Production of brominated rubber and brominated rubber composition |
| JPS55131002A (en) | 1979-03-30 | 1980-10-11 | Japan Synthetic Rubber Co Ltd | Crystalline brominated 1,2-polybutadiene and preparation thereof |
| JPS5841302B2 (ja) | 1980-12-29 | 1983-09-10 | アキレス株式会社 | 難燃性を有する発泡性ポリスチレン樹脂組成物 |
| DE4213164A1 (de) | 1992-04-22 | 1993-10-28 | Bayer Ag | Verfahren zur Herstellung von bromiertem chlorsubstituiertem Poly-1,3-butadien |
| JPH06322023A (ja) * | 1993-05-14 | 1994-11-22 | Manac Inc | 回収した発泡ポリスチレンを原料とする臭素化ポリスチレンの製造方法 |
| GB0407463D0 (en) | 2004-04-01 | 2004-05-05 | Nova Chem Int Sa | Extruded foam structure with an inorganic blowing agent |
| US8114943B2 (en) * | 2006-08-16 | 2012-02-14 | Dow Global Technologies Llc | Process for brominating butadiene/vinyl aromatic copolymers |
-
2006
- 2006-10-23 AU AU2006315878A patent/AU2006315878A1/en not_active Abandoned
- 2006-10-23 BR BRPI0619699-3A patent/BRPI0619699A2/pt not_active Application Discontinuation
- 2006-10-23 US US12/091,346 patent/US7851558B2/en active Active
- 2006-10-23 CN CN2006800422261A patent/CN101305022B/zh active Active
- 2006-10-23 DE DE602006011944T patent/DE602006011944D1/de active Active
- 2006-10-23 WO PCT/US2006/041295 patent/WO2007058736A1/en not_active Ceased
- 2006-10-23 HR HR20080206A patent/HRP20080206A2/xx not_active Application Discontinuation
- 2006-10-23 KR KR1020087011118A patent/KR20080066787A/ko not_active Withdrawn
- 2006-10-23 JP JP2008540035A patent/JP5302001B2/ja active Active
- 2006-10-23 CA CA2627253A patent/CA2627253C/en active Active
- 2006-10-23 AT AT06836467T patent/ATE455796T1/de not_active IP Right Cessation
- 2006-10-23 RU RU2008123837/04A patent/RU2414479C2/ru active
- 2006-10-23 EP EP06836467A patent/EP1957544B1/en active Active
- 2006-10-23 ES ES06836467T patent/ES2336951T3/es active Active
-
2008
- 2008-04-25 NO NO20081960A patent/NO20081960L/no not_active Application Discontinuation
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1301497B (de) * | 1966-01-05 | 1969-08-21 | Basf Ag | Verfahren zur Herstellung bromierter Polymerisate des Butadiens |
| DD137308A3 (de) * | 1969-09-24 | 1979-08-29 | Paul Herte | Verfahren zur herstellung von bromierten ungesaettigten niedermolekularen polymeren |
| GB1474536A (en) * | 1973-07-30 | 1977-05-25 | Shell Int Research | Halogenated partially hydrogenated block copolymer and its preparation |
| SU597687A1 (ru) * | 1976-03-09 | 1978-03-15 | Предприятие П/Я В-2756 | Бромированный бутадиен-нитрильный каучук как огнестойка добавка в полимерных композици х |
| US5532322A (en) * | 1995-09-26 | 1996-07-02 | Manac Inc. | Process for preparing brominated polystyrene |
| US5532322B1 (en) * | 1995-09-26 | 1999-12-07 | Manac Inc | Process for preparing brominated polystyrene |
| RU2177952C2 (ru) * | 1999-03-23 | 2002-01-10 | Щербань Георгий Трофимович | Способ получения галоидированного бутилкаучука |
Non-Patent Citations (1)
| Title |
|---|
| Е.Buzdugan, P.Ghioca, E.G.Badea, S.Serban "Bromination of some styrene-diene block copolymers" Eur. Polym. J., vol.33, №10-12, pp.1713-1716, 1997. * |
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| WO2020139111A1 (en) | 2018-12-27 | 2020-07-02 | Public Joint Stock Company "Sibur Holding" | Modified diene-containing (co)polymer, method for producing the same and use of the same as a flame retardant |
| WO2020139110A1 (en) | 2018-12-27 | 2020-07-02 | Public Joint Stock Company "Sibur Holding" | Modified (co)polymer, method for preparing thereof and use of the same |
| WO2020139112A1 (en) | 2018-12-27 | 2020-07-02 | Public Joint Stock Company "Sibur Holding" | Modified diene-containing (co)polymer, method for preparing thereof and use as a flame retardant |
| WO2020139114A1 (en) | 2018-12-27 | 2020-07-02 | Public Joint Stock Company "Sibur Holding" | Modified diene-containing (co)polymer, method for preparing thereof and use of the same as flame retardant |
| WO2020139113A1 (en) | 2018-12-27 | 2020-07-02 | Public Joint Stock Company "Sibur Holding" | Modified diene-containing (co)polymer, method for preparing thereof and use of the same as flame retardant |
| RU2794096C2 (ru) * | 2018-12-27 | 2023-04-11 | Публичное акционерное общество "СИБУР Холдинг" | Модифицированный диенсодержащий (cо)полимер, способ его получения и применение в качестве антипирена |
| US12180308B2 (en) | 2018-12-27 | 2024-12-31 | Public Joint Stock Company “SIBUR Holding” | Modified (co)polymer, method for preparing thereof and use of the same |
| US12203025B2 (en) | 2018-12-27 | 2025-01-21 | Public Joint Stock Company “SIBUR Holding” | Modified diene-containing (co)polymer, method for preparing thereof and use as a flame retardant |
Also Published As
| Publication number | Publication date |
|---|---|
| NO20081960L (no) | 2008-08-11 |
| DE602006011944D1 (de) | 2010-03-11 |
| RU2008123837A (ru) | 2009-12-27 |
| HRP20080206A2 (hr) | 2008-08-31 |
| ATE455796T1 (de) | 2010-02-15 |
| BRPI0619699A2 (pt) | 2011-10-11 |
| CN101305022B (zh) | 2012-06-20 |
| WO2007058736A1 (en) | 2007-05-24 |
| EP1957544B1 (en) | 2010-01-20 |
| US7851558B2 (en) | 2010-12-14 |
| JP2009516019A (ja) | 2009-04-16 |
| CA2627253A1 (en) | 2007-05-24 |
| CN101305022A (zh) | 2008-11-12 |
| US20080287559A1 (en) | 2008-11-20 |
| KR20080066787A (ko) | 2008-07-16 |
| EP1957544A1 (en) | 2008-08-20 |
| JP5302001B2 (ja) | 2013-10-02 |
| ES2336951T3 (es) | 2010-04-19 |
| CA2627253C (en) | 2013-11-19 |
| AU2006315878A1 (en) | 2007-05-24 |
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