GB1001837A - Organic aluminium compounds - Google Patents
Organic aluminium compoundsInfo
- Publication number
- GB1001837A GB1001837A GB15563A GB15563A GB1001837A GB 1001837 A GB1001837 A GB 1001837A GB 15563 A GB15563 A GB 15563A GB 15563 A GB15563 A GB 15563A GB 1001837 A GB1001837 A GB 1001837A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compounds
- organic
- aluminium
- atoms
- aluminoxanes
- 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.)
- Expired
Links
- 150000001399 aluminium compounds Chemical class 0.000 title abstract 3
- 229940077746 antacid containing aluminium compound Drugs 0.000 title abstract 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 9
- 125000005842 heteroatom Chemical group 0.000 abstract 8
- -1 aluminium alkoxide Chemical class 0.000 abstract 6
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 abstract 6
- 238000010438 heat treatment Methods 0.000 abstract 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 5
- 150000001735 carboxylic acids Chemical class 0.000 abstract 5
- 150000002440 hydroxy compounds Chemical class 0.000 abstract 5
- 239000000203 mixture Substances 0.000 abstract 5
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 abstract 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 abstract 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 4
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 abstract 4
- 229910052796 boron Inorganic materials 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 abstract 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 abstract 4
- 229910019142 PO4 Inorganic materials 0.000 abstract 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 abstract 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 abstract 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 239000007789 gas Substances 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 150000002894 organic compounds Chemical class 0.000 abstract 3
- 239000001301 oxygen Substances 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 150000002989 phenols Chemical class 0.000 abstract 3
- 235000021317 phosphate Nutrition 0.000 abstract 3
- 229910052698 phosphorus Inorganic materials 0.000 abstract 3
- 239000011574 phosphorus Substances 0.000 abstract 3
- 229920001228 polyisocyanate Polymers 0.000 abstract 3
- 239000005056 polyisocyanate Substances 0.000 abstract 3
- 229920000642 polymer Polymers 0.000 abstract 3
- 229910052718 tin Inorganic materials 0.000 abstract 3
- 239000011135 tin Substances 0.000 abstract 3
- 229910052719 titanium Inorganic materials 0.000 abstract 3
- 239000010936 titanium Substances 0.000 abstract 3
- 229910052725 zinc Inorganic materials 0.000 abstract 3
- 239000011701 zinc Substances 0.000 abstract 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 abstract 2
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 abstract 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 2
- 239000005792 Geraniol Substances 0.000 abstract 2
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 abstract 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 abstract 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 abstract 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 abstract 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000001279 adipic acids Chemical class 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 150000004703 alkoxides Chemical class 0.000 abstract 2
- 125000005600 alkyl phosphonate group Chemical group 0.000 abstract 2
- 239000004411 aluminium Substances 0.000 abstract 2
- 229910052782 aluminium Inorganic materials 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 229910052787 antimony Inorganic materials 0.000 abstract 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 abstract 2
- 235000019445 benzyl alcohol Nutrition 0.000 abstract 2
- 150000003938 benzyl alcohols Chemical class 0.000 abstract 2
- 229910052797 bismuth Inorganic materials 0.000 abstract 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 abstract 2
- 150000001642 boronic acid derivatives Chemical class 0.000 abstract 2
- 229910052793 cadmium Inorganic materials 0.000 abstract 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract 2
- 150000001734 carboxylic acid salts Chemical class 0.000 abstract 2
- 229960000541 cetyl alcohol Drugs 0.000 abstract 2
- 229910017052 cobalt Inorganic materials 0.000 abstract 2
- 239000010941 cobalt Substances 0.000 abstract 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- 239000010949 copper Substances 0.000 abstract 2
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 abstract 2
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 2
- HHFAWKCIHAUFRX-UHFFFAOYSA-N ethoxide Chemical compound CC[O-] HHFAWKCIHAUFRX-UHFFFAOYSA-N 0.000 abstract 2
- 239000003925 fat Substances 0.000 abstract 2
- 229940113087 geraniol Drugs 0.000 abstract 2
- 229910052742 iron Inorganic materials 0.000 abstract 2
- VQPKAMAVKYTPLB-UHFFFAOYSA-N lead;octanoic acid Chemical compound [Pb].CCCCCCCC(O)=O VQPKAMAVKYTPLB-UHFFFAOYSA-N 0.000 abstract 2
- 229910052749 magnesium Inorganic materials 0.000 abstract 2
- 239000011777 magnesium Substances 0.000 abstract 2
- 150000002691 malonic acids Chemical class 0.000 abstract 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 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 229910052750 molybdenum Inorganic materials 0.000 abstract 2
- 239000011733 molybdenum Substances 0.000 abstract 2
- 229910052759 nickel Inorganic materials 0.000 abstract 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 2
- 229940055577 oleyl alcohol Drugs 0.000 abstract 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 abstract 2
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 abstract 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 abstract 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 2
- 229960005235 piperonyl butoxide Drugs 0.000 abstract 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- IKNCGYCHMGNBCP-UHFFFAOYSA-N propan-1-olate Chemical compound CCC[O-] IKNCGYCHMGNBCP-UHFFFAOYSA-N 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 abstract 2
- CQRYARSYNCAZFO-UHFFFAOYSA-N salicyl alcohol Chemical class OCC1=CC=CC=C1O CQRYARSYNCAZFO-UHFFFAOYSA-N 0.000 abstract 2
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000007858 starting material Substances 0.000 abstract 2
- 150000003444 succinic acids Chemical class 0.000 abstract 2
- 229910052715 tantalum Inorganic materials 0.000 abstract 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 abstract 2
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 abstract 2
- 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 abstract 2
- 229910052720 vanadium Inorganic materials 0.000 abstract 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 abstract 2
- 229910052726 zirconium Inorganic materials 0.000 abstract 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 abstract 1
- ICMJHPBQTVWCNT-UHFFFAOYSA-N 1-(dibutylamino)propan-2-ol Chemical compound CCCCN(CC(C)O)CCCC ICMJHPBQTVWCNT-UHFFFAOYSA-N 0.000 abstract 1
- YAXQOLYGKLGQKA-UHFFFAOYSA-N 1-morpholin-4-ylpropan-2-ol Chemical compound CC(O)CN1CCOCC1 YAXQOLYGKLGQKA-UHFFFAOYSA-N 0.000 abstract 1
- QCYOIFVBYZNUNW-UHFFFAOYSA-N 2-(dimethylazaniumyl)propanoate Chemical compound CN(C)C(C)C(O)=O QCYOIFVBYZNUNW-UHFFFAOYSA-N 0.000 abstract 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 abstract 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 abstract 1
- CMIZMQJYGMWWII-UHFFFAOYSA-N 3-[bis(2-phenylethyl)amino]propan-1-ol Chemical compound OCCCN(CCC1=CC=CC=C1)CCC1=CC=CC=C1 CMIZMQJYGMWWII-UHFFFAOYSA-N 0.000 abstract 1
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 abstract 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 abstract 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 1
- 108010077895 Sarcosine Proteins 0.000 abstract 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 abstract 1
- QYIBXNARBGCCNX-UHFFFAOYSA-N [V+3].CCCC[O-].CCCC[O-].CCCC[O-] Chemical compound [V+3].CCCC[O-].CCCC[O-].CCCC[O-] QYIBXNARBGCCNX-UHFFFAOYSA-N 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 235000011037 adipic acid Nutrition 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
- 239000003963 antioxidant agent Substances 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- BSDOQSMQCZQLDV-UHFFFAOYSA-N butan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] BSDOQSMQCZQLDV-UHFFFAOYSA-N 0.000 abstract 1
- JTZFNJUMDPPGBY-UHFFFAOYSA-L cadmium(2+);propanoate Chemical compound [Cd+2].CCC([O-])=O.CCC([O-])=O JTZFNJUMDPPGBY-UHFFFAOYSA-L 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 230000001413 cellular effect Effects 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 229940076286 cupric acetate Drugs 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 239000003063 flame retardant Substances 0.000 abstract 1
- 239000006260 foam Substances 0.000 abstract 1
- 229910052732 germanium Inorganic materials 0.000 abstract 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 abstract 1
- KYXIMMOBOGDUFW-UHFFFAOYSA-N germanium zirconium Chemical compound [Ge].[Zr] KYXIMMOBOGDUFW-UHFFFAOYSA-N 0.000 abstract 1
- 239000004220 glutamic acid Substances 0.000 abstract 1
- 235000013922 glutamic acid Nutrition 0.000 abstract 1
- 150000002307 glutamic acids Chemical class 0.000 abstract 1
- 150000002311 glutaric acids Chemical class 0.000 abstract 1
- 150000002334 glycols Chemical class 0.000 abstract 1
- 229910001385 heavy metal Inorganic materials 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 239000012948 isocyanate Substances 0.000 abstract 1
- SRJOCJYGOFTFLH-UHFFFAOYSA-N isonipecotic acid Chemical compound OC(=O)C1CCNCC1 SRJOCJYGOFTFLH-UHFFFAOYSA-N 0.000 abstract 1
- 229940046892 lead acetate Drugs 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 150000002736 metal compounds Chemical class 0.000 abstract 1
- 229930182817 methionine Natural products 0.000 abstract 1
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 abstract 1
- 235000001968 nicotinic acid Nutrition 0.000 abstract 1
- 229960003512 nicotinic acid Drugs 0.000 abstract 1
- 239000011664 nicotinic acid Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 239000004014 plasticizer Substances 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- OGHBATFHNDZKSO-UHFFFAOYSA-N propan-2-olate Chemical compound CC(C)[O-] OGHBATFHNDZKSO-UHFFFAOYSA-N 0.000 abstract 1
- 229940043230 sarcosine Drugs 0.000 abstract 1
- 235000011044 succinic acid Nutrition 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 150000003512 tertiary amines Chemical class 0.000 abstract 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical class OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 abstract 1
- WOZZOSDBXABUFO-UHFFFAOYSA-N tri(butan-2-yloxy)alumane Chemical compound [Al+3].CCC(C)[O-].CCC(C)[O-].CCC(C)[O-] WOZZOSDBXABUFO-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000001993 wax Substances 0.000 abstract 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 abstract 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
-
- 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/069—Aluminium compounds without C-aluminium linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Polyurethanes Or Polyureas (AREA)
Abstract
The invention comprises organic aluminoxanes in which some of the aluminium atoms are replaced by " hetero " atoms selected from copper, magnesium, zinc, cadmium, germanium, zirconium, titanium, tin, lead, vanadium, antimony, tantalum, bismuth, molybdenum, manganese, iron, cobalt, nickel, boron and phosphorus. They are obtained by heating an aluminium alkoxide or phenoxide with at least one organic hydroxy compound, at least one carboxylic acid and at least one compound containing the hetero atom linked to an organic radical through oxygen or a -COO- radical, at least the later stages of the heating being carried out at a temperature exceeding 140 DEG C. Suitable aluminium compounds in use as starting materials are, for example, the ethoxide, propoxide, isopropoxide, butoxide and phenoxide. Suitable hydroxy compounds for use in the manufacture of the required compounds are alkanols, oleyl alcohol, cetyl alcohol, geraniol, cyclohexanol, benzyl alcohol, furfuryl alcohol, substituted benzyl alcohols, phenol and substituted phenols, polyoxyalkylene alcohols such as hydroxy-ended polymers or copolymers of cyclic oxides, ethylene glycol, propylene glycol, di-, tri- or tetraethylene glycols, glycerol or methylol phenols. Suitable carboxylic acids are, for example, acetic, propionic, butyric, octoic, nonanoic, decanoic, oleic, linoleic, stearic, ricinoleic, malonic, succinic, adipic and glutamic acids. Hydroxyl compounds and carboxylic acids derived from naturally occurring fats and oils may also be used. The hydroxyl compounds and carboxylic acids may contain amino groups. Suitable organic compounds containing the metallic hetero atoms include alkoxides and carboxylic acid salts. Suitable organic compounds containing boron or phosphorus are, for example, trialkyl borates, dialkyl alkyl boronates, dialkyl alkyl phosphonates, trialkyl phosphites, trialkyl phosphates and dialkyl hydrogen phosphonates. The products may have a cyclic, linear or co-ordinated structure depending on the proportions of starting materials used. The aluminoxanes of the invention are useful as surfactant additives for use in the manufacture of foamed cellular polyurethane materials by the reaction of organic polyisocyanates and polymers containing at least two hudroxy groups per molecule under such conditions that a foam-forming gas is generated. The polymers containing at least two hydroxyl groups per molecule include linear and branched polyesters, polyethers and polyesteramides. Suitable organic polyisocyanates include aliphatic and aromatic di- and tri-isocyanates. The foam-forming gas may be carbon dioxide generated by the reaction of some of the polyisocyanate with water which has been added to the mixture or it may be generated by incorporating in the mixture a suitable low boiling liquid which on heating will volatilize to give the foam-forming gas. In addition to one of the aluminoxanes of the invention, there may also be present in the mixture catalysts, e.g. tertiary amines or soluble heavy metal compounds, surface-ative agents, flame-retardants, plasticizers, fillers or antioxidants. The aluminoxane is normally used in the foam-forming mixture in an amount of 0.01-10% by weight. In the Examples: (a) a reaction product of isooctanol and propylene oxide (N.Wr. 850) is added to aluminium secbutoxide; nonarol and methoxypolyethylene glycol are added and after heating 2-ethyl hexoic acid and lead octoate are added to give an aluminoxane containing lead; (b) similar reactions were carried out to obtain aluminoxanes containing zinc, tin, titanium, zirconium, boron and phosphorus; (c) the products of Examples (a) and (b) above are added to an oxypropylated glycerol (approx. mol. wt. 3000), and to the mixture are added tolylene diisocyanates and aqueous solutions of dimethyl-amino pyridine and stannous octoate; a low density flexible foam is formed.ALSO:The invention comprises organic aluminoxanes which contain in addition to aluminium atoms one or more "hetero" atoms selected from copper, magnesium, zinc, cadmium, germanium-zirconium, titanium, tin, lead, vanadium, antimony, tantalum, bismuth, molybdenum, manganese, iron, cobalt, nickel, boron and phosphones. The aluminoxanes are defined as having structures of alternate oxygen and aluminium atoms with one or more of the aluminium atoms being replaced by one or more of the "hetero" atoms and may be of cyclic, linear or co-ordinate structure. The aluminoxanes of the invention may be obtained by heating an aluminium alkoxide or phenoxide with an organic hydroxy compound, a carboxylic acid and a compound containing the hetero atom linked to an organic radical through oxygen or a -COO- radical, at least the later stages of the heating being carried out at a temperature exceeding 140 DEG C. Suitable starting aluminium compounds are, for example, the ethoxide, propoxide, butoxide and phenoxide. The alcohols or phenols used include, for example, alkanols, oleyl alcohol, cetyl alcohol, geraniol, cyclohexanol, benzyl alcohol, furfuryl alcohol, substituted benzyl alcohols, phenol and substituted phenols, glycols, polyethylene glycols, glycerol and methylol phenols. Suitable carboxylic acids are, for example, acetic, propionic, butyric, octoic, nonanoic, decanoic, oleic, linoleic, stearic, ricinoleic, malonic, succinic, adipic and glutaric acids. Hydroxy compounds and acids derived from naturally occurring fats and waxes may also be used. A proportion of the carboxylic acid may be replaced by an organic sulphonic acid, a phosphoric acid or an acid phosphate ester. The hydroxy compounds or carboxylic acids used may contain amino groups, e.g. N-2-hydroxypropyl-di-n-butylamine, N-hydroxypropyl - di - (2 - phenylethyl) - amine, N - 2 - hydroxypropylmorpholine, N-hydroxyethyldiethylamine, sarcosine, nicotinic acid, piperidine-4-carboxylic acid, serine, methionine and N,N - dimethylaminopropionic acid. Suitable organic compounds containing the metallic hetero-atoms include alkoxides and carboxylic acid salts, e.g. titanium tetraisopropoxide, zirconium tetra-n-butoxide, vanadium tri-n-butoxide, zinc octoate, lead acetate, lead octoate, cadmium propionate, stannous octoate and cupric acetate. Examples of suitable compounds containing non-metallic hetero-atoms include trialkyl borates, dialkyl alkyl boronates, dialkyl alkyl phosphonates, trialkyl phosphites, trialkyl phosphates and dialkyl hydrogen phosphonates.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB15563A GB1001837A (en) | 1963-01-01 | 1963-01-01 | Organic aluminium compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB15563A GB1001837A (en) | 1963-01-01 | 1963-01-01 | Organic aluminium compounds |
Publications (1)
Publication Number | Publication Date |
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GB1001837A true GB1001837A (en) | 1965-08-18 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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GB15563A Expired GB1001837A (en) | 1963-01-01 | 1963-01-01 | Organic aluminium compounds |
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GB (1) | GB1001837A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011064292A3 (en) * | 2009-11-25 | 2011-07-21 | Dsm Ip Assets B.V. | Polyester amide foamers |
US20120271087A1 (en) * | 2011-04-20 | 2012-10-25 | Nova Chemicals (International) S.A. | Activation for Oligomerization |
-
1963
- 1963-01-01 GB GB15563A patent/GB1001837A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011064292A3 (en) * | 2009-11-25 | 2011-07-21 | Dsm Ip Assets B.V. | Polyester amide foamers |
CN102725377A (en) * | 2009-11-25 | 2012-10-10 | 帝斯曼知识产权资产管理有限公司 | Polyester amide foamers |
US20130045898A1 (en) * | 2009-11-25 | 2013-02-21 | Dsm Ip Assets B.V. | Polyester amide foamers |
US20120271087A1 (en) * | 2011-04-20 | 2012-10-25 | Nova Chemicals (International) S.A. | Activation for Oligomerization |
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