NO850021L - Polymersammensetning - Google Patents

Polymersammensetning

Info

Publication number: NO850021L
Authority: NO; Norway
Prior art keywords: silanol condensation; condensation catalyst; silyl; finely divided; solid material
Prior art date: 1984-01-05

Application number

NO850021A

Other languages

English (en)

Norwegian (no)

Inventor

Jaffrey David Umpleby

Original Assignee

Bp Chem Int Ltd

Priority date (The priority date 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 date listed.)

1984-01-05

Filing date

1985-01-03

Publication date

1985-07-08

1985-01-03 Application filed by Bp Chem Int Ltd filed Critical Bp Chem Int Ltd

1985-07-08 Publication of NO850021L publication Critical patent/NO850021L/no

Links

239000000203 mixture Substances 0.000 title claims abstract description 55
229920000642 polymer Polymers 0.000 title claims abstract description 8
239000003054 catalyst Substances 0.000 claims abstract description 53
238000009833 condensation Methods 0.000 claims abstract description 50
230000005494 condensation Effects 0.000 claims abstract description 50
SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims abstract description 49
239000003707 silyl modified polymer Substances 0.000 claims abstract description 37
239000011343 solid material Substances 0.000 claims abstract description 20
238000004132 cross linking Methods 0.000 claims abstract description 16
229920001169 thermoplastic Polymers 0.000 claims abstract description 12
239000004416 thermosoftening plastic Substances 0.000 claims abstract description 12
238000007334 copolymerization reaction Methods 0.000 claims abstract description 11
238000001125 extrusion Methods 0.000 claims abstract description 10
239000002245 particle Substances 0.000 claims abstract description 8
239000011148 porous material Substances 0.000 claims abstract description 5
-1 unsaturated silane compound Chemical class 0.000 claims description 32
229920001577 copolymer Polymers 0.000 claims description 26
238000000034 method Methods 0.000 claims description 25
239000005977 Ethylene Substances 0.000 claims description 22
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 21
239000012876 carrier material Substances 0.000 claims description 17
238000002156 mixing Methods 0.000 claims description 13
239000000463 material Substances 0.000 claims description 11
239000003999 initiator Substances 0.000 claims description 10
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 9
150000003254 radicals Chemical class 0.000 claims description 9
150000001463 antimony compounds Chemical class 0.000 claims description 8
229910052698 phosphorus Inorganic materials 0.000 claims description 8
239000011574 phosphorus Substances 0.000 claims description 8
239000004698 Polyethylene Substances 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 7
239000007788 liquid Substances 0.000 claims description 7
229920000573 polyethylene Polymers 0.000 claims description 7
229920000578 graft copolymer Polymers 0.000 claims description 6
229920001567 vinyl ester resin Polymers 0.000 claims description 6
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
150000001252 acrylic acid derivatives Chemical class 0.000 claims description 5
150000002170 ethers Chemical class 0.000 claims description 4
150000002825 nitriles Chemical class 0.000 claims description 4
125000001424 substituent group Chemical group 0.000 claims description 4
239000004711 α-olefin Substances 0.000 claims description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
239000011248 coating agent Substances 0.000 claims description 3
238000000576 coating method Methods 0.000 claims description 3
238000009413 insulation Methods 0.000 claims description 3
239000002904 solvent Substances 0.000 claims description 3
238000010521 absorption reaction Methods 0.000 claims description 2
229910052787 antimony Chemical group 0.000 claims description 2
WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical group [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
238000010438 heat treatment Methods 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
238000011065 in-situ storage Methods 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
230000002028 premature Effects 0.000 abstract description 7
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract description 6
238000003856 thermoforming Methods 0.000 abstract description 5
238000005809 transesterification reaction Methods 0.000 abstract description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
239000012141 concentrate Substances 0.000 description 10
229920000620 organic polymer Polymers 0.000 description 10
238000004519 manufacturing process Methods 0.000 description 8
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 7
239000000654 additive Substances 0.000 description 6
239000012975 dibutyltin dilaurate Substances 0.000 description 6
229910000077 silane Inorganic materials 0.000 description 6
150000002500 ions Chemical class 0.000 description 5
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical group CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
125000003545 alkoxy group Chemical group 0.000 description 4
NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
239000000377 silicon dioxide Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
239000011135 tin Substances 0.000 description 4
229910052718 tin Inorganic materials 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 3
238000007796 conventional method Methods 0.000 description 3
238000007765 extrusion coating Methods 0.000 description 3
239000007789 gas Substances 0.000 description 3
125000001183 hydrocarbyl group Chemical group 0.000 description 3
239000000178 monomer Substances 0.000 description 3
125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 3
150000003018 phosphorus compounds Chemical class 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
150000004756 silanes Chemical class 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-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
229920000181 Ethylene propylene rubber Polymers 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical compound CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 description 2
238000010096 film blowing Methods 0.000 description 2
238000005470 impregnation Methods 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
238000001746 injection moulding Methods 0.000 description 2
239000011133 lead Substances 0.000 description 2
239000000155 melt Substances 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
239000007870 radical polymerization initiator Substances 0.000 description 2
238000003860 storage Methods 0.000 description 2
238000012360 testing method Methods 0.000 description 2
XTTGYFREQJCEML-UHFFFAOYSA-N tributyl phosphite Chemical compound CCCCOP(OCCCC)OCCCC XTTGYFREQJCEML-UHFFFAOYSA-N 0.000 description 2
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical class CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
ORIHZIZPTZTNCU-VMPITWQZSA-N 2-[(E)-hydroxyiminomethyl]phenol Chemical compound O\N=C\C1=CC=CC=C1O ORIHZIZPTZTNCU-VMPITWQZSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
235000006650 Syzygium cordatum Nutrition 0.000 description 1
240000005572 Syzygium cordatum Species 0.000 description 1
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
HRIMTTNYSCTIDV-UHFFFAOYSA-L [dibutyl(hexadecanoyloxy)stannyl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCCCCCC HRIMTTNYSCTIDV-UHFFFAOYSA-L 0.000 description 1
YVHDRFKHKGNLNW-UHFFFAOYSA-L [dibutyl(octadecanoyloxy)stannyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCCCCCCCC YVHDRFKHKGNLNW-UHFFFAOYSA-L 0.000 description 1
NBJODVYWAQLZOC-UHFFFAOYSA-L [dibutyl(octanoyloxy)stannyl] octanoate Chemical compound CCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCC NBJODVYWAQLZOC-UHFFFAOYSA-L 0.000 description 1
XQBCVRSTVUHIGH-UHFFFAOYSA-L [dodecanoyloxy(dioctyl)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCCCCCC)(CCCCCCCC)OC(=O)CCCCCCCCCCC XQBCVRSTVUHIGH-UHFFFAOYSA-L 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000004645 aluminates Chemical class 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
DBLFQTDPPZZDGX-UHFFFAOYSA-N bis(6-methylheptoxy)-oxophosphanium Chemical compound CC(C)CCCCCO[P+](=O)OCCCCCC(C)C DBLFQTDPPZZDGX-UHFFFAOYSA-N 0.000 description 1
238000000071 blow moulding Methods 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
238000003490 calendering Methods 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000012159 carrier gas Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000012461 cellulose resin Substances 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
229920006037 cross link polymer Polymers 0.000 description 1
230000007547 defect Effects 0.000 description 1
JQZRVMZHTADUSY-UHFFFAOYSA-L di(octanoyloxy)tin Chemical compound [Sn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O JQZRVMZHTADUSY-UHFFFAOYSA-L 0.000 description 1
PNOXNTGLSKTMQO-UHFFFAOYSA-L diacetyloxytin Chemical compound CC(=O)O[Sn]OC(C)=O PNOXNTGLSKTMQO-UHFFFAOYSA-L 0.000 description 1
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 1
239000006185 dispersion Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical group 0.000 description 1
FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
150000003947 ethylamines Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
239000010439 graphite Substances 0.000 description 1
229910002804 graphite Inorganic materials 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
229920001903 high density polyethylene Polymers 0.000 description 1
239000004700 high-density polyethylene Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
229910052588 hydroxylapatite Inorganic materials 0.000 description 1
238000007654 immersion Methods 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
238000010102 injection blow moulding Methods 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
229920000092 linear low density polyethylene Polymers 0.000 description 1
239000004707 linear low-density polyethylene Substances 0.000 description 1
229920001684 low density polyethylene Polymers 0.000 description 1
239000004702 low-density polyethylene Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
239000001095 magnesium carbonate Substances 0.000 description 1
229910000021 magnesium carbonate Inorganic materials 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
239000006078 metal deactivator Substances 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
LGRRJJDVUWUDST-UHFFFAOYSA-N methyl 4-trimethoxysilylbutanoate Chemical compound COC(=O)CCC[Si](OC)(OC)OC LGRRJJDVUWUDST-UHFFFAOYSA-N 0.000 description 1
239000011707 mineral Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
229920005615 natural polymer Polymers 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229910052755 nonmetal Inorganic materials 0.000 description 1
150000002843 nonmetals Chemical class 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
150000001451 organic peroxides Chemical class 0.000 description 1
MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 1
150000003003 phosphines Chemical class 0.000 description 1
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
238000002459 porosimetry Methods 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000001175 rotational moulding Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000004065 semiconductor Substances 0.000 description 1
150000004819 silanols Chemical class 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000004634 thermosetting polymer Substances 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
DSKYTPNZLCVELA-UHFFFAOYSA-N trihexyl phosphite Chemical compound CCCCCCOP(OCCCCCC)OCCCCCC DSKYTPNZLCVELA-UHFFFAOYSA-N 0.000 description 1
QUTZUATVZPXUJR-UHFFFAOYSA-N trinonyl phosphite Chemical compound CCCCCCCCCOP(OCCCCCCCCC)OCCCCCCCCC QUTZUATVZPXUJR-UHFFFAOYSA-N 0.000 description 1
HVYVMSPIJIWUNA-UHFFFAOYSA-N triphenylstibine Chemical compound C1=CC=CC=C1[Sb](C=1C=CC=CC=1)C1=CC=CC=C1 HVYVMSPIJIWUNA-UHFFFAOYSA-N 0.000 description 1
CIOXFKGQNIJXKF-UHFFFAOYSA-N tris(2-methoxyethoxy)silane Chemical compound COCCO[SiH](OCCOC)OCCOC CIOXFKGQNIJXKF-UHFFFAOYSA-N 0.000 description 1
DECPGQLXYYCNEZ-UHFFFAOYSA-N tris(6-methylheptyl) phosphite Chemical compound CC(C)CCCCCOP(OCCCCCC(C)C)OCCCCCC(C)C DECPGQLXYYCNEZ-UHFFFAOYSA-N 0.000 description 1
230000000007 visual effect Effects 0.000 description 1
239000010457 zeolite Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
229910001928 zirconium oxide Inorganic materials 0.000 description 1

Classifications

- 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
- C08F4/00—Polymerisation catalysts
- 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
- C08K5/54—Silicon-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
- C08K9/00—Use of pretreated ingredients
- C08K9/12—Adsorbed ingredients, e.g. ingredients on carriers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/10—Block- or graft-copolymers containing polysiloxane sequences

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Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Compositions Of Macromolecular Compounds (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Organic Insulating Materials (AREA)
Catalysts (AREA)
Silicon Polymers (AREA)

NO850021A 1984-01-05 1985-01-03 Polymersammensetning NO850021L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB848400150A GB8400150D0 (en)	1984-01-05	1984-01-05	Polymer composition

Publications (1)

Publication Number	Publication Date
NO850021L true NO850021L (no)	1985-07-08

Family

ID=10554563

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO850021A NO850021L (no)	1984-01-05	1985-01-03	Polymersammensetning

Country Status (5)

Country	Link
EP (1)	EP0150595A3 (fr)
JP (1)	JPS60170628A (fr)
KR (1)	KR850005473A (fr)
GB (1)	GB8400150D0 (fr)
NO (1)	NO850021L (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9103802D0 (en) *	1991-02-23	1991-04-10	Bp Chem Int Ltd	Crosslinkable polymeric composition
FR2937461B1 (fr)	2008-10-21	2014-02-14	Axon Cable Sa	Cable et/ou cordon convenant pour une utilisation en milieu hospitalier ou dans un environnement a atmosphere controlee et leur procede de fabrication
JP2017112026A (ja) *	2015-12-18	2017-06-22	聖森山	被覆電線

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1044400B (de) *	1956-04-02	1958-11-20	Union Carbide Corp	Verfahren zur Herstellung von Organopolysiloxanelastomeren
JPS559611A (en) *	1978-07-05	1980-01-23	Mitsubishi Petrochem Co Ltd	Cross-linkable polyethylene resin composition
US4292423A (en) *	1979-04-19	1981-09-29	Wacker-Chemie Gmbh	Process for the preparation of organopolysiloxanes

1984
- 1984-01-05 GB GB848400150A patent/GB8400150D0/en active Pending
- 1984-12-13 EP EP84308673A patent/EP0150595A3/fr not_active Ceased
1985
- 1985-01-03 NO NO850021A patent/NO850021L/no unknown
- 1985-01-04 JP JP60000088A patent/JPS60170628A/ja active Pending
- 1985-01-05 KR KR1019850000024A patent/KR850005473A/ko not_active Withdrawn

Also Published As

Publication number	Publication date
EP0150595A2 (fr)	1985-08-07
GB8400150D0 (en)	1984-02-08
JPS60170628A (ja)	1985-09-04
KR850005473A (ko)	1985-08-26
EP0150595A3 (fr)	1985-08-21

Publication	Publication Date	Title
CA1265285A (fr)	1990-01-30	Composition de polymere modifie de sylyle presentant une diminution des reactions prematurees de polymerisation
EP0351106B1 (fr)	1995-04-26	Composition d'un polymère silylé réticulable
EP0004034B1 (fr)	1984-02-15	Méthode de réticulation de résines de la série des alpha-polyoléfines
EP0207627A2 (fr)	1987-01-07	Composition de polymères
KR930009332B1 (ko)	1993-09-27	중합체 조성물 및 그의 제조방법
EP0004752A2 (fr)	1979-10-17	Copolymère alcène-alkylacrylate, modifié par des groupes silanes, réticulable par l'eau, procédé pour sa préparation et produits fabriqués à l'aide de ce copolymère
EP2388294B1 (fr)	2013-05-29	Composition polyoléfinique comprenant une polyoléfine réticulable avec des groupes silanes, un catalyseur de condensation au silanol et un composé contenant du silicium
US5420208A (en)	1995-05-30	Crosslinkable polymeric composition
US5028680A (en)	1991-07-02	Crosslinkable silyl polymer composition
CN110540710A (zh)	2019-12-06	一种耐热老化聚丙烯纳米复合材料及其制备方法
US4975480A (en)	1990-12-04	Crosslinkable silyl polymer composition
NO850021L (no)	1985-07-08	Polymersammensetning
EP1862501A1 (fr)	2007-12-05	Un composé de silicium comme un auxiliaire de traitement dans les compositions polyolefiniques
WO1992021721A1 (fr)	1992-12-10	Composition polymere reticulable
AU671809B2 (en)	1996-09-12	Crosslinkable polymeric composition
JPH02175710A (ja)	1990-07-09	エチレン・プロピレン系弾性共重合体の製造方法