FI64388C - Polyvinylkloridfoereningar vilka aer stabiliserade med ringformiga alfa-acylketoner - Google Patents
Polyvinylkloridfoereningar vilka aer stabiliserade med ringformiga alfa-acylketoner Download PDFInfo
- Publication number
- FI64388C FI64388C FI763329A FI763329A FI64388C FI 64388 C FI64388 C FI 64388C FI 763329 A FI763329 A FI 763329A FI 763329 A FI763329 A FI 763329A FI 64388 C FI64388 C FI 64388C
- Authority
- FI
- Finland
- Prior art keywords
- group
- groups
- cycloaliphatic
- carbon atoms
- weight
- Prior art date
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 12
- 239000004800 polyvinyl chloride Substances 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 239000003381 stabilizer Substances 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 150000002894 organic compounds Chemical class 0.000 claims description 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 238000012986 modification Methods 0.000 claims description 4
- 230000004048 modification Effects 0.000 claims description 4
- 230000000087 stabilizing effect Effects 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 125000004450 alkenylene group Chemical group 0.000 claims description 3
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 3
- 150000001805 chlorine compounds Chemical class 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims 3
- 206010008631 Cholera Diseases 0.000 claims 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003607 modifier Substances 0.000 claims 1
- 210000005036 nerve Anatomy 0.000 claims 1
- 230000002611 ovarian Effects 0.000 claims 1
- 230000006641 stabilisation Effects 0.000 claims 1
- 238000011105 stabilization Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 20
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 8
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 7
- -1 acyl ketones Chemical class 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 239000000314 lubricant Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- XHLHPRDBBAGVEG-UHFFFAOYSA-N 1-tetralone Chemical compound C1=CC=C2C(=O)CCCC2=C1 XHLHPRDBBAGVEG-UHFFFAOYSA-N 0.000 description 2
- UVKSTCWQLPZZSN-UHFFFAOYSA-N 2-octadecyl-3,4-dihydro-2H-naphthalen-1-one Chemical compound C1=CC=C2C(=O)C(CCCCCCCCCCCCCCCCCC)CCC2=C1 UVKSTCWQLPZZSN-UHFFFAOYSA-N 0.000 description 2
- KCKZIWSINLBROE-UHFFFAOYSA-N 3,4-dihydro-1h-naphthalen-2-one Chemical compound C1=CC=C2CC(=O)CCC2=C1 KCKZIWSINLBROE-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- FLIACVVOZYBSBS-UHFFFAOYSA-N Methyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC FLIACVVOZYBSBS-UHFFFAOYSA-N 0.000 description 2
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 2
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229910000104 sodium hydride Inorganic materials 0.000 description 2
- 239000012312 sodium hydride Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- VEDOFWZOFCKNRQ-UHFFFAOYSA-N 1-acetyl-3,4-dihydro-1h-naphthalen-2-one Chemical compound C1=CC=C2C(C(=O)C)C(=O)CCC2=C1 VEDOFWZOFCKNRQ-UHFFFAOYSA-N 0.000 description 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 description 1
- OEKATORRSPXJHE-UHFFFAOYSA-N 2-acetylcyclohexan-1-one Chemical compound CC(=O)C1CCCCC1=O OEKATORRSPXJHE-UHFFFAOYSA-N 0.000 description 1
- YTVQIZRDLKWECQ-UHFFFAOYSA-N 2-benzoylcyclohexan-1-one Chemical compound C=1C=CC=CC=1C(=O)C1CCCCC1=O YTVQIZRDLKWECQ-UHFFFAOYSA-N 0.000 description 1
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-hydroxyoctadecanoic acid Chemical class CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- GMHMQAPTTHYDMR-UHFFFAOYSA-N C(C(C(CO)(CO)CO)O)C(O)(O)O Chemical compound C(C(C(CO)(CO)CO)O)C(O)(O)O GMHMQAPTTHYDMR-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 150000001661 cadmium Chemical class 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000012674 dispersion polymerization Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
- 238000010101 extrusion blow moulding Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 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
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000006053 organic reaction Methods 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000001175 rotational moulding Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010189 synthetic method Methods 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
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/455—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation with carboxylic acids or their derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/385—Saturated compounds containing a keto group being part of a ring
- C07C49/403—Saturated compounds containing a keto group being part of a ring of a six-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/657—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings
- C07C49/665—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings a keto group being part of a condensed ring system
- C07C49/67—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings a keto group being part of a condensed ring system having two rings, e.g. tetralones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
- C07C49/782—Ketones containing a keto group bound to a six-membered aromatic ring polycyclic
- C07C49/792—Ketones containing a keto group bound to a six-membered aromatic ring polycyclic containing rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Materials For Medical Uses (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7615869 | 1976-05-20 | ||
| FR7615869A FR2352025A2 (fr) | 1976-05-20 | 1976-05-20 | Compositions stabilisees a base de chlorure de polyvinyle |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI763329A7 FI763329A7 (en。) | 1977-11-21 |
| FI64388B FI64388B (fi) | 1983-07-29 |
| FI64388C true FI64388C (fi) | 1983-11-10 |
Family
ID=9173647
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI763329A FI64388C (fi) | 1976-05-20 | 1976-11-19 | Polyvinylkloridfoereningar vilka aer stabiliserade med ringformiga alfa-acylketoner |
Country Status (19)
| Country | Link |
|---|---|
| JP (2) | JPS52141855A (en。) |
| AR (1) | AR227265A1 (en。) |
| AT (1) | AT346077B (en。) |
| AU (1) | AU508095B2 (en。) |
| BE (1) | BE848450R (en。) |
| CH (1) | CH609079A5 (en。) |
| DD (1) | DD127311A6 (en。) |
| DE (1) | DE2652458C3 (en。) |
| DK (1) | DK119877A (en。) |
| FI (1) | FI64388C (en。) |
| FR (1) | FR2352025A2 (en。) |
| GB (1) | GB1525787A (en。) |
| IT (1) | IT1123635B (en。) |
| LU (1) | LU76200A1 (en。) |
| NL (1) | NL177923C (en。) |
| NO (1) | NO146712C (en。) |
| NZ (1) | NZ182754A (en。) |
| SE (1) | SE415570B (en。) |
| ZA (1) | ZA767149B (en。) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS54137044A (en) * | 1978-04-17 | 1979-10-24 | Adeka Argus Chem Co Ltd | Halogen-containing resin composition |
| JPS5571744A (en) * | 1978-11-24 | 1980-05-30 | Sakai Chem Ind Co Ltd | Chlorine-containing resin composition |
| FR2456132A2 (fr) * | 1979-05-10 | 1980-12-05 | Rhone Poulenc Ind | Compositions stabilisees a base de chlorure de polyvinyle |
| JPS5699254A (en) * | 1980-01-14 | 1981-08-10 | Adeka Argus Chem Co Ltd | Stabilized halogen-containing resin composition |
| US4774839A (en) * | 1982-12-27 | 1988-10-04 | American National Can Company | Method and apparatus for necking containers |
| JPS6127126A (ja) * | 1984-07-16 | 1986-02-06 | Daiwa Can Co Ltd | 多段ネツクイン缶の製法 |
| JPS6169012U (en。) * | 1984-10-09 | 1986-05-12 | ||
| JPS61206533A (ja) * | 1985-03-09 | 1986-09-12 | Machiyama Seisakusho:Kk | エアゾ−ル缶の成形方法 |
| IT1295100B1 (it) | 1997-09-16 | 1999-04-30 | Interplastica Srl | Materiale sintetico e procedimento per la produzione dello stesso |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2307075A (en) * | 1940-08-02 | 1943-01-05 | Carbide And Carbon Chemicais C | Vinyl resin composition |
| US2669548A (en) * | 1951-01-02 | 1954-02-16 | Monsanto Chemicals | Stabilized halogen-containing resins |
| GB1054583A (en。) * | 1963-07-02 | |||
| NL131106C (en。) * | 1964-01-22 | |||
| FR1480549A (fr) * | 1965-05-21 | 1967-05-12 | Carlisle Chemical Works | Compositions résineuses stabilisées contenant des composés métalliques |
| CH464521A (de) * | 1965-05-21 | 1968-10-31 | Carlisle Chemical Works | Verfahren zur Aufhebung der Lichtempfindlichkeit von plastischen Massen, die Antimon- oder Wismutverbindungen enthalten |
| US3492267A (en) * | 1966-12-02 | 1970-01-27 | Grace W R & Co | Stabilizing poly(vinyl chloride) |
| JPS4833977A (en。) * | 1971-09-07 | 1973-05-15 | ||
| JPS5615666B2 (en。) * | 1973-11-15 | 1981-04-11 | ||
| FR2297227A1 (fr) * | 1975-01-10 | 1976-08-06 | Rhone Poulenc Ind | Compositions stabilisees a base de chlorure de polyvinyle |
| FR2324681A2 (fr) * | 1975-09-22 | 1977-04-15 | Rhone Poulenc Ind | Compositions stabilisees a base de chlorure de polyvinyle |
| JPS579386A (en) * | 1980-06-20 | 1982-01-18 | Sumitomo Metal Ind | Pipe joint |
-
1976
- 1976-05-20 FR FR7615869A patent/FR2352025A2/fr active Granted
- 1976-11-15 LU LU76200A patent/LU76200A1/xx unknown
- 1976-11-17 DE DE2652458A patent/DE2652458C3/de not_active Expired
- 1976-11-17 BE BE172457A patent/BE848450R/xx not_active IP Right Cessation
- 1976-11-19 CH CH1459176A patent/CH609079A5/xx not_active IP Right Cessation
- 1976-11-19 FI FI763329A patent/FI64388C/fi not_active IP Right Cessation
- 1976-11-23 NL NLAANVRAGE7613052,A patent/NL177923C/xx not_active IP Right Cessation
- 1976-11-24 GB GB49006/76A patent/GB1525787A/en not_active Expired
- 1976-11-25 DD DD195964A patent/DD127311A6/xx unknown
- 1976-11-26 AR AR265625A patent/AR227265A1/es active
- 1976-11-29 NZ NZ182754A patent/NZ182754A/xx unknown
- 1976-11-29 IT IT29904/76A patent/IT1123635B/it active
- 1976-11-30 ZA ZA767149A patent/ZA767149B/xx unknown
- 1976-12-01 AU AU20168/76A patent/AU508095B2/en not_active Expired
- 1976-12-01 AT AT891476A patent/AT346077B/de active
-
1977
- 1977-01-31 JP JP962177A patent/JPS52141855A/ja active Pending
- 1977-03-18 SE SE7702932A patent/SE415570B/xx not_active IP Right Cessation
- 1977-03-18 DK DK119877A patent/DK119877A/da not_active Application Discontinuation
- 1977-03-21 NO NO770988A patent/NO146712C/no unknown
-
1982
- 1982-01-21 JP JP57006873A patent/JPS5841311B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2352025A2 (fr) | 1977-12-16 |
| GB1525787A (en) | 1978-09-20 |
| JPS52141855A (en) | 1977-11-26 |
| ATA891476A (de) | 1978-02-15 |
| BE848450R (fr) | 1977-05-17 |
| NZ182754A (en) | 1978-11-13 |
| NO146712B (no) | 1982-08-16 |
| SE7702932L (sv) | 1977-11-21 |
| DK119877A (da) | 1977-11-21 |
| JPS57141442A (en) | 1982-09-01 |
| AR227265A1 (es) | 1982-10-15 |
| FI763329A7 (en。) | 1977-11-21 |
| IT1123635B (it) | 1986-04-30 |
| NO770988L (no) | 1977-11-22 |
| AT346077B (de) | 1978-10-25 |
| DD127311A6 (en。) | 1977-09-14 |
| JPS5841311B2 (ja) | 1983-09-10 |
| FI64388B (fi) | 1983-07-29 |
| AU2016876A (en) | 1978-06-08 |
| NO146712C (no) | 1982-11-24 |
| CH609079A5 (en) | 1979-02-15 |
| DE2652458B2 (de) | 1978-09-07 |
| ZA767149B (en) | 1977-10-26 |
| DE2652458A1 (de) | 1977-12-01 |
| NL177923C (nl) | 1985-12-16 |
| FR2352025B2 (en。) | 1980-09-19 |
| AU508095B2 (en) | 1980-03-06 |
| NL177923B (nl) | 1985-07-16 |
| DE2652458C3 (de) | 1986-02-13 |
| SE415570B (sv) | 1980-10-13 |
| NL7613052A (nl) | 1977-11-22 |
| LU76200A1 (en。) | 1977-12-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed | ||
| MM | Patent lapsed |
Owner name: RHONE- POULENC INDUSTRIES |