DE1923088A1 - Organische Peroxyde und Verfahren zu deren Herstellung - Google Patents
Organische Peroxyde und Verfahren zu deren HerstellungInfo
- Publication number
- DE1923088A1 DE1923088A1 DE19691923088 DE1923088A DE1923088A1 DE 1923088 A1 DE1923088 A1 DE 1923088A1 DE 19691923088 DE19691923088 DE 19691923088 DE 1923088 A DE1923088 A DE 1923088A DE 1923088 A1 DE1923088 A1 DE 1923088A1
- Authority
- DE
- Germany
- Prior art keywords
- carbon atoms
- radical
- groups
- peroxide
- compounds according
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 10
- 150000001451 organic peroxides Chemical class 0.000 title claims description 4
- 238000004519 manufacturing process Methods 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 229920000642 polymer Polymers 0.000 claims description 8
- 150000002978 peroxides Chemical class 0.000 claims description 7
- 125000000864 peroxy group Chemical group O(O*)* 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 150000002432 hydroperoxides Chemical class 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 239000007795 chemical reaction product Substances 0.000 claims 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 claims 1
- 239000005062 Polybutadiene Substances 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- 239000004793 Polystyrene Substances 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 229920002678 cellulose Polymers 0.000 claims 1
- 239000001913 cellulose Substances 0.000 claims 1
- 239000007859 condensation product Substances 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000002993 cycloalkylene group Chemical group 0.000 claims 1
- XPBOFLGWLULIJL-UHFFFAOYSA-N dioxepane-3,7-dione Chemical compound O=C1CCCC(=O)OO1 XPBOFLGWLULIJL-UHFFFAOYSA-N 0.000 claims 1
- 229920002857 polybutadiene Polymers 0.000 claims 1
- 229920000515 polycarbonate Polymers 0.000 claims 1
- 239000004417 polycarbonate Substances 0.000 claims 1
- 229920000570 polyether Polymers 0.000 claims 1
- 229920002223 polystyrene Polymers 0.000 claims 1
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000000460 chlorine Substances 0.000 description 8
- -1 chloroformyl Chemical group 0.000 description 7
- 238000005660 chlorination reaction Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 150000008064 anhydrides Chemical group 0.000 description 2
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- IYCFUFRXCCCTSX-UHFFFAOYSA-N tert-butyl 3-carbonochloridoyloxypropaneperoxoate Chemical compound CC(C)(C)OOC(=O)CCOC(Cl)=O IYCFUFRXCCCTSX-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- UQSXEMVUGMPGLS-UHFFFAOYSA-N 2-tert-butylperoxycarbonylbenzoic acid Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1C(O)=O UQSXEMVUGMPGLS-UHFFFAOYSA-N 0.000 description 1
- XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- QROYGCALYMMPQS-UHFFFAOYSA-M C(=O)[O-].[Br+] Chemical compound C(=O)[O-].[Br+] QROYGCALYMMPQS-UHFFFAOYSA-M 0.000 description 1
- 125000006414 CCl Chemical group ClC* 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001263 acyl chlorides Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 230000002140 halogenating effect Effects 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- DRRXNWSIUMXFPX-UHFFFAOYSA-N tert-butyl 3-hydroxypropaneperoxoate Chemical compound CC(C)(C)OOC(=O)CCO DRRXNWSIUMXFPX-UHFFFAOYSA-N 0.000 description 1
- NOECWXWMZVUICW-UHFFFAOYSA-N tert-butyl 4-chloro-4-oxobut-2-eneperoxoate Chemical compound CC(C)(C)OOC(=O)C=CC(Cl)=O NOECWXWMZVUICW-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/16—Peroxy compounds the —O—O— group being bound between two carbon atoms not further substituted by oxygen atoms, i.e. peroxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/20—Peroxy compounds the —O—O— group being bound to a carbon atom further substituted by singly—bound oxygen atoms
- C07C409/22—Peroxy compounds the —O—O— group being bound to a carbon atom further substituted by singly—bound oxygen atoms having two —O—O— groups bound to the carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/32—Peroxy compounds the —O—O— group being bound between two >C=O groups
- C07C409/34—Peroxy compounds the —O—O— group being bound between two >C=O groups both belonging to carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/38—Peroxy compounds the —O—O— group being bound between a >C=O group and a carbon atom, not further substituted by oxygen atoms, i.e. esters of peroxy acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C409/00—Peroxy compounds
- C07C409/42—Peroxy compounds containing sulfur atoms
- C07C409/44—Peroxy compounds containing sulfur atoms with sulfur atoms directly bound to the —O—O— groups, e.g. persulfonic acids
-
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
- C08C19/34—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups
- C08C19/38—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with oxygen or oxygen-containing groups with hydroxy radicals
-
- 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
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
- C08F291/18—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00 on to irradiated or oxidised macromolecules
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/06—Oxidation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/10—Acylation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G67/00—Macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing oxygen or oxygen and carbon, not provided for in groups C08G2/00 - C08G65/00
-
- 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
- C08F2810/00—Chemical modification of a polymer
- C08F2810/40—Chemical modification of a polymer taking place solely at one end or both ends of the polymer backbone, i.e. not in the side or lateral chains
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S522/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S522/904—Monomer or polymer contains initiating group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Cosmetics (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US727323A US3671651A (en) | 1968-05-07 | 1968-05-07 | Peroxy compounds containing a haloformate group |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1923088A1 true DE1923088A1 (de) | 1970-08-06 |
Family
ID=24922212
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19691923088 Pending DE1923088A1 (de) | 1968-05-07 | 1969-05-06 | Organische Peroxyde und Verfahren zu deren Herstellung |
| DE19691965870 Pending DE1965870A1 (de) | 1968-05-07 | 1969-05-06 | Organische peroxyhaltige Polymere und Verfahren zu deren Herstellung |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19691965870 Pending DE1965870A1 (de) | 1968-05-07 | 1969-05-06 | Organische peroxyhaltige Polymere und Verfahren zu deren Herstellung |
Country Status (6)
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3671651A (en) * | 1968-05-07 | 1972-06-20 | Pennwalt Corp | Peroxy compounds containing a haloformate group |
| US4029685A (en) * | 1973-08-15 | 1977-06-14 | The Dow Chemical Company | Peroxy esters of pyromellitic acid |
| US4129700A (en) * | 1975-07-17 | 1978-12-12 | Pennwalt Corporation | Peroxy compounds and vulcanizable compositions thereof |
| US4155956A (en) * | 1977-03-14 | 1979-05-22 | Galina Ballova | Process for producing shock-proof graft copolymers of styrene with synthetic rubber |
| JPS5920666B2 (ja) * | 1977-05-31 | 1984-05-15 | 日本油脂株式会社 | エステル結合を有するジアシル型ポリメリックペオキシドおよびそれを有効成分とする重合開始剤 |
| US4165432A (en) * | 1977-10-18 | 1979-08-21 | Olin Corporation | Peroxy di-ester polyols |
| US4179271A (en) * | 1977-12-14 | 1979-12-18 | Texaco Inc. | Amine oxide polymers and use thereof as fuel detergent |
| US4315082A (en) * | 1978-01-03 | 1982-02-09 | Fmc Corporation | Phosphorus compounds |
| JPS557855A (en) * | 1978-07-04 | 1980-01-21 | Nippon Oil & Fats Co Ltd | Preparation of non-aqueous polymer dispersion |
| US4218548A (en) * | 1978-08-28 | 1980-08-19 | Pennwalt Corporation | Peroxy compounds and vulcanizable compositions thereof |
| JPS5562913A (en) * | 1978-11-01 | 1980-05-12 | Nippon Oil & Fats Co Ltd | Production of cast-polymerized methyl methacrylate milk white plate |
| JPS5575414A (en) * | 1978-11-30 | 1980-06-06 | Nippon Oil & Fats Co Ltd | Polymer or copolymer having peroxy bond in molecule |
| US4469862A (en) * | 1982-07-05 | 1984-09-04 | Nippon Oil And Fats Co. Ltd. | Polymeric diacyl peroxides |
| JPS59197401A (ja) * | 1983-04-26 | 1984-11-09 | Nippon Oil & Fats Co Ltd | 光重合開始剤 |
| JPS59202261A (ja) * | 1983-04-30 | 1984-11-16 | Nippon Oil & Fats Co Ltd | 高分子材料の表面改質法 |
| US4525308A (en) * | 1983-05-20 | 1985-06-25 | Pennwalt Corporation | Hydroxy-t-alkyl peroxyesters |
| DE3643792A1 (de) * | 1986-12-20 | 1988-06-23 | Bayer Ag | Polymere emulgatoren auf basis aminotelecheler oligomere i |
| US4956416A (en) * | 1988-08-18 | 1990-09-11 | Atochem North America, Inc. | Amino or hydrazino peroxides, derivatives and their uses |
| US5272219A (en) * | 1988-08-18 | 1993-12-21 | Elf Atochem North America, Inc. | Process for preparing amino or hydrazino peroxides, derivatives and their uses |
| JPH02140211A (ja) * | 1988-11-22 | 1990-05-29 | Nippon Oil & Fats Co Ltd | 分子内にペルオキシ給合を有するマレイミド系共重合体 |
| CA2005835A1 (en) * | 1989-01-30 | 1990-07-30 | Jose Sanchez | Hydroxy-peroxides and their uses |
| US5387654A (en) * | 1993-01-08 | 1995-02-07 | Elf Atochem North America, Inc. | Hydroxy-peroxides and their uses |
| US5043414A (en) * | 1989-08-28 | 1991-08-27 | General Electric Company | Alkylperoxyformate-terminated polycarbonate |
| US5191058A (en) * | 1989-09-07 | 1993-03-02 | General Electric Company | Preparation of peroxide terminated polycarbonate |
| CA2021109A1 (en) * | 1989-09-07 | 1991-03-08 | Edward J. Fewkes, (Jr.) | Peroxide-terminated polycarbonates, preparation thereof and conversion to copolymers |
| US5039754A (en) * | 1990-08-30 | 1991-08-13 | Atochem North America, Inc. | Polymeric peroxides derived from hydroxy-hydroperoxides and dihydroxydialkyl peroxides and their uses |
| NO912922L (no) * | 1990-09-05 | 1992-03-06 | Atochem North America | Peroksyder for polymeriseringsreaksjoner. |
| US5219930A (en) * | 1990-09-21 | 1993-06-15 | Quantum Chemical Corporation | Process for converting vinyl alcohol polymers to poly(keto-esters) therefrom |
| DE4030599C2 (de) * | 1990-09-27 | 1995-09-14 | Eastman Kodak Co | Thermolabiles Polymer |
| ES2095068T3 (es) * | 1992-08-07 | 1997-02-01 | Akzo Nobel Nv | Peroxicarbonatos polimericos y procedimiento para prepararlos. |
| US5314970A (en) * | 1993-01-07 | 1994-05-24 | Elf Atochem North America, Inc. | OO-t-alkyl O-polycaprolactone monoperoxycarbonates |
| US5475072A (en) * | 1994-02-09 | 1995-12-12 | Elf Atochem North America, Inc. | Unsaturated peroxide compositions, polymeric-peroxides derived therefrom and their uses |
| US5981787A (en) * | 1996-12-30 | 1999-11-09 | Elf Atochem North America, Inc. | Peroxyoxalates derived from hydroxy-hydroperoxides |
| US5866712A (en) * | 1996-12-30 | 1999-02-02 | Elf Atochem North America, Inc. | Oxalic acid peroxide compositions and uses |
| FR3041645B1 (fr) * | 2015-09-29 | 2017-09-08 | Arkema France | Polymerisation radicalaire de l'ethylene amorcee par un couple de peroxydes organiques a haute productivite |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2476637A (en) * | 1947-02-28 | 1949-07-19 | Pittsburgh Plate Glass Co | Method of preparing chloroformates |
| US2659716A (en) * | 1952-10-24 | 1953-11-17 | Monsanto Chemicals | Vinyl halide polymerization with adipoyl peroxide and hexamethylene diamine |
| US2978495A (en) * | 1955-08-22 | 1961-04-04 | Aerojet General Co | Nitramino esters |
| US3165546A (en) * | 1962-09-27 | 1965-01-12 | Eastman Kodak Co | Diaryl peroxides by reaction of hypochlorites on corresponding hydroperoxides |
| NL284315A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1962-10-12 | |||
| US3288855A (en) * | 1963-03-25 | 1966-11-29 | Monsanto Res Corp | Fluorinated diones |
| US3646108A (en) * | 1965-09-23 | 1972-02-29 | Ici Ltd | Fibre-forming polymers |
| US3632630A (en) * | 1967-08-17 | 1972-01-04 | Atlantic Richfield Co | Diesters of aromatic dihydroxy carbonyl compounds and branched chain fatty acids containing a quaternary carbon atom |
| US3652520A (en) * | 1968-03-22 | 1972-03-28 | Atlantic Richfield Co | Polymers of polymerizable polydiene ethylenically unsaturated esters |
| US3671651A (en) * | 1968-05-07 | 1972-06-20 | Pennwalt Corp | Peroxy compounds containing a haloformate group |
| US3652724A (en) * | 1969-02-27 | 1972-03-28 | Sumitomo Chemical Co | Process for producing block copolymers |
-
1968
- 1968-05-07 US US727323A patent/US3671651A/en not_active Expired - Lifetime
-
1969
- 1969-05-06 DE DE19691923088 patent/DE1923088A1/de active Pending
- 1969-05-06 DE DE19691965870 patent/DE1965870A1/de active Pending
- 1969-05-07 GB GB23258/69A patent/GB1241891A/en not_active Expired
- 1969-05-07 NL NL6907013A patent/NL6907013A/xx unknown
- 1969-05-07 FR FR6914526A patent/FR2007984A1/fr not_active Withdrawn
-
1971
- 1971-12-10 CA CA129,896A patent/CA970895A/en not_active Expired
- 1971-12-22 US US05/211,093 patent/US4304882A/en not_active Expired - Lifetime
-
1974
- 1974-07-31 US US05/493,369 patent/US3952041A/en not_active Expired - Lifetime
-
1976
- 1976-01-12 US US05/648,216 patent/US3991109A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US3991109A (en) | 1976-11-09 |
| US3671651A (en) | 1972-06-20 |
| FR2007984A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1970-01-16 |
| GB1241891A (en) | 1971-08-04 |
| US4304882A (en) | 1981-12-08 |
| CA970895A (en) | 1975-07-08 |
| DE1965870A1 (de) | 1970-09-17 |
| US3952041A (en) | 1976-04-20 |
| NL6907013A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1969-11-11 |
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