GB1406419A - Metal phosphate coating or organic polymers - Google Patents
Metal phosphate coating or organic polymersInfo
- Publication number
- GB1406419A GB1406419A GB4761474A GB4761474A GB1406419A GB 1406419 A GB1406419 A GB 1406419A GB 4761474 A GB4761474 A GB 4761474A GB 4761474 A GB4761474 A GB 4761474A GB 1406419 A GB1406419 A GB 1406419A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymers
- metal
- coating
- phosphate
- oxyacid
- 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
- 238000000576 coating method Methods 0.000 title abstract 9
- 239000011248 coating agent Substances 0.000 title abstract 6
- 229910001463 metal phosphate Inorganic materials 0.000 title abstract 4
- 229920000620 organic polymer Polymers 0.000 title abstract 4
- 229920001688 coating polymer Polymers 0.000 title 1
- 229920000642 polymer Polymers 0.000 abstract 9
- 229910019142 PO4 Inorganic materials 0.000 abstract 5
- 235000021317 phosphate Nutrition 0.000 abstract 5
- -1 polysiloxanes Polymers 0.000 abstract 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 4
- 229920001577 copolymer Polymers 0.000 abstract 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 4
- 239000010452 phosphate Substances 0.000 abstract 4
- 229910052698 phosphorus Inorganic materials 0.000 abstract 4
- 239000011574 phosphorus Substances 0.000 abstract 4
- 239000000758 substrate Substances 0.000 abstract 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000002148 esters Chemical class 0.000 abstract 3
- 150000002736 metal compounds Chemical class 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 239000002904 solvent Substances 0.000 abstract 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- 239000004952 Polyamide Substances 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000003085 diluting agent Substances 0.000 abstract 2
- 150000004820 halides Chemical class 0.000 abstract 2
- 150000002576 ketones Chemical class 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 229920005615 natural polymer Polymers 0.000 abstract 2
- 150000002828 nitro derivatives Chemical class 0.000 abstract 2
- 229920002492 poly(sulfone) Polymers 0.000 abstract 2
- 229920002647 polyamide Polymers 0.000 abstract 2
- 229920000515 polycarbonate Polymers 0.000 abstract 2
- 239000004417 polycarbonate Substances 0.000 abstract 2
- 229920000728 polyester Polymers 0.000 abstract 2
- VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 abstract 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 abstract 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 abstract 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- 229920000571 Nylon 11 Polymers 0.000 abstract 1
- 229920002292 Nylon 6 Polymers 0.000 abstract 1
- 229920002302 Nylon 6,6 Polymers 0.000 abstract 1
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 1
- 229920002396 Polyurea Polymers 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 abstract 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
- 150000001242 acetic acid derivatives Chemical class 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 150000004703 alkoxides Chemical class 0.000 abstract 1
- 125000005250 alkyl acrylate group Chemical group 0.000 abstract 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 abstract 1
- 229910002091 carbon monoxide Inorganic materials 0.000 abstract 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 abstract 1
- 229910052804 chromium Inorganic materials 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- 239000003086 colorant Substances 0.000 abstract 1
- 150000001913 cyanates Chemical class 0.000 abstract 1
- 150000004292 cyclic ethers Chemical class 0.000 abstract 1
- 150000001993 dienes Chemical class 0.000 abstract 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 abstract 1
- 235000011180 diphosphates Nutrition 0.000 abstract 1
- 238000007598 dipping method Methods 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 abstract 1
- 239000000835 fiber Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 abstract 1
- 150000004675 formic acid derivatives Chemical class 0.000 abstract 1
- 239000008187 granular material Substances 0.000 abstract 1
- 150000008282 halocarbons Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 150000004679 hydroxides Chemical class 0.000 abstract 1
- 150000002500 ions Chemical class 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 239000003446 ligand Substances 0.000 abstract 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical group 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- 150000002823 nitrates Chemical class 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 150000003891 oxalate salts Chemical class 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 abstract 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 abstract 1
- 150000003003 phosphines Chemical class 0.000 abstract 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 abstract 1
- 229920002239 polyacrylonitrile Polymers 0.000 abstract 1
- 229920000570 polyether Polymers 0.000 abstract 1
- 229920000139 polyethylene terephthalate Polymers 0.000 abstract 1
- 239000005020 polyethylene terephthalate Substances 0.000 abstract 1
- 239000002861 polymer material Substances 0.000 abstract 1
- 229920000098 polyolefin Polymers 0.000 abstract 1
- 229920006324 polyoxymethylene Polymers 0.000 abstract 1
- 229920006380 polyphenylene oxide Polymers 0.000 abstract 1
- 229920001296 polysiloxane Polymers 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000005507 spraying Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 229920001059 synthetic polymer Polymers 0.000 abstract 1
- 150000003568 thioethers Chemical class 0.000 abstract 1
- 229910052719 titanium Inorganic materials 0.000 abstract 1
- 229910052720 vanadium Inorganic materials 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 1
- 229920001959 vinylidene polymer Polymers 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002023 wood Substances 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
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/048—Forming gas barrier coatings
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/06—Coating with compositions not containing macromolecular substances
-
- 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
- C08J2325/06—Polystyrene
-
- 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
- C08J2325/08—Copolymers of styrene
- C08J2325/12—Copolymers of styrene with unsaturated nitriles
-
- 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
- C08J2369/00—Characterised by the use of polycarbonates; Derivatives of polycarbonates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Paper (AREA)
- Laminated Bodies (AREA)
Abstract
1406419 Metal phosphates IMPERIAL CHEMICAL INDUSTRIES Ltd 11 Sept 1972 [20 July 1971 29 Oct 1971 4 Nov 1971 26 Nov 1971 (2) 20 Dec 1971 2 June 1972] 47614/74 47615/74 47616/74 47617/74 47618/74 47619/74 and 47620/74 Divided out of 1406233 Heading C1A [Also in Division B2] Organic polymer substrate has a coating comprising at least one metal phosphate, the metal having an atomic number of 12, 14, 20-32, 39-50, 56-80, 90 or 92, the phosphate being derived from an oxyacid of phosphorus having the structure where X<SP>1</SP> and X<SP>2</SP> are the same or different and are selected from hydrogen, hydroxide and halide and in which X<SP>2</SP> may have the structure Phosphates of Fe, Ti, Cr and V are specifically mentioned to provide pyrophosphate. The coating may be produced by applying to the organic polymer substrate a coating composition comprising a solution of the compound of the metal and an oxyacid of phosphorus or a compound capable of forming such an oxyacid in a solvent which comprises at least in part an organic component and heating the coating to produce the metal phosphate. The organic solvent is preferably an alcohol, ester, ketone, aldehyde, nitro-compound or ether especially monohydric alcohols ROH and esters of the structure R<SP>1</SP>COOR<SP>2</SP> where R, R<SP>1</SP> and R<SP>2</SP> are alkyl groups or substituted alkyl groups containing 1-10 carbon atoms, ethers of the structure R<SP>1</SP>OR<SP>2</SP> and ketones of the structure R<SP>1</SP>COR<SP>2</SP>, nitro-compounds of the structure R<SP>1</SP>NO 2 and cyclic ethers of the structure OR<SP>3</SP> where R<SP>3</SP> is a divalent alkyl group having 4-7 carbon atoms one of which may be replaced by an oxygen atom. Numerous suitable specific compounds are listed. Two or more solvents may be used and diluents may be present such as aromatic or halogenated hydrocarbons. The composition may be formed by dissolving a metal compound and an oxyacid of phosphorus, or a source thereof, such as the anhydride or oxyhalide, in a solvent for at least one component and for the reaction product in the presence of an organic diluent. The metal compound may be phosphate and so provide the oxyacid of phosphorus in which case an additional acid may be required. Suitable metal compounds are oxides, hydroxides, halides, carbonates, nitrates, perchlorates and cyanates. Salts of organic acids such as acetates, benzoates, oxalates, propionates or formates may also be used as well as alkoxides and co-ordination complexes such as those having ligands derived from acetyl acetone, ethylene dithiol, ethanolamine, carbon monoxide or phosphines. Other components such as pigments, polymers, colorants, surfactants or sources of other ions and other additives may be included. Suitable polymers are diene polymers, acetylene polymers, vinyl and vinylidene polymers, such as acrylic acid and methacrylic acid polymers, acrylic and methacrylic polymers, polyacrylonitrile, polyethers, polysulphones, formaldehyde resins, polyesters, polycarbonates, polyamides, polyureas and polyurethanes, natural polymers and modified natural polymers and polysiloxanes. The organic polymer substrate may be in the form of a fibre, filament, sheet, film, granule or powder and may be applied by dipping, spraying, roller or brush. The coating may be up to 10 microns thick but what is preferably 0À01 to 5 microns thick. Thicker coatings may be obtained by repeated application of the compositions. The substrates to which the compositions may be applied include cellulosic polymers such as wood and paper and synthetic polymers such a polyolefines, e.g. polymers and copolymers of ethylene, propylene, butadiene, isoprene, 4-methylpentene-1 and styrene, copolymers of ethylene with unsaturated esters such as vinyl acetate or alkyl acrylates, methacrylates, modified styrene copolymers such as styrene-maleic anhydride and styrene-acrylonitrile copolymers, polymers and copolymers of other ethylenically unsaturated monomers such as vinyl chloride, vinylidene chloride, chloroprene, methyl methacrylate, ethyl acrylate, vinyl acetate, polyphenylene oxides and sulphides, polysulphones, polyoxymethylenes, polyamides, such as nylon 6, nylon 6-6 and nylon 11, polycarbonates and polyesters such as polyethylene 1,2-diphenoxyethane - 4,4<SP>1 </SP>- dicarboxylate and polyethylene terephthalate. The phosphate coatings may form a primer or outer coating for the surface of the polymer material which should be painted, printed or metallized or further coated with one or more phosphate coatings.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4761474A GB1406419A (en) | 1971-07-20 | 1971-07-20 | Metal phosphate coating or organic polymers |
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4761474A GB1406419A (en) | 1971-07-20 | 1971-07-20 | Metal phosphate coating or organic polymers |
GB4761574 | 1971-10-29 | ||
GB4761674 | 1971-11-04 | ||
GB4761774 | 1971-11-26 | ||
GB4761874 | 1971-11-26 | ||
GB4761974 | 1971-12-20 | ||
GB4762074 | 1972-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1406419A true GB1406419A (en) | 1975-09-17 |
Family
ID=27562653
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4761474A Expired GB1406419A (en) | 1971-07-20 | 1971-07-20 | Metal phosphate coating or organic polymers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1406419A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0010366A1 (en) * | 1978-09-26 | 1980-04-30 | Occidental Research Corporation | Solid organometallic inorganic polymers and their application |
US4298723A (en) | 1978-09-26 | 1981-11-03 | Occidental Research Corporation | Layered or amorphous acyclic organometallic inorganic polymers |
US4299943A (en) | 1980-03-25 | 1981-11-10 | Occidental Research Corporation | Nonaqueous preparation of layered or amorphous organometallic inorganic polymers |
US4390690A (en) | 1979-07-24 | 1983-06-28 | Occidental Research Corp. | Layered organophosphorous inorganic polymers containing oxygen bonded to carbon |
US4429111A (en) | 1979-07-24 | 1984-01-31 | Occidental Research Corporation | Layered organophosphorus inorganic polymers containing mixed functional groups |
CN111655301A (en) * | 2018-02-09 | 2020-09-11 | 普罗米米克公司 | Zirconium and titanium phosphate coatings for implants and other substrates |
-
1971
- 1971-07-20 GB GB4761474A patent/GB1406419A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0010366A1 (en) * | 1978-09-26 | 1980-04-30 | Occidental Research Corporation | Solid organometallic inorganic polymers and their application |
US4298723A (en) | 1978-09-26 | 1981-11-03 | Occidental Research Corporation | Layered or amorphous acyclic organometallic inorganic polymers |
US4390690A (en) | 1979-07-24 | 1983-06-28 | Occidental Research Corp. | Layered organophosphorous inorganic polymers containing oxygen bonded to carbon |
US4429111A (en) | 1979-07-24 | 1984-01-31 | Occidental Research Corporation | Layered organophosphorus inorganic polymers containing mixed functional groups |
US4299943A (en) | 1980-03-25 | 1981-11-10 | Occidental Research Corporation | Nonaqueous preparation of layered or amorphous organometallic inorganic polymers |
CN111655301A (en) * | 2018-02-09 | 2020-09-11 | 普罗米米克公司 | Zirconium and titanium phosphate coatings for implants and other substrates |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PCNP | Patent ceased through non-payment of renewal fee |