DE1104700B - Verfahren zur Herstellung von Polymerisationskunststoffen - Google Patents
Verfahren zur Herstellung von PolymerisationskunststoffenInfo
- Publication number
- DE1104700B DE1104700B DER25925A DER0025925A DE1104700B DE 1104700 B DE1104700 B DE 1104700B DE R25925 A DER25925 A DE R25925A DE R0025925 A DER0025925 A DE R0025925A DE 1104700 B DE1104700 B DE 1104700B
- Authority
- DE
- Germany
- Prior art keywords
- compounds
- plastics
- radical
- ethylidene
- alkyl radical
- 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
- 229920003023 plastic Polymers 0.000 title claims description 10
- 239000004033 plastic Substances 0.000 title claims description 10
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000000034 method Methods 0.000 title claims description 7
- 239000000178 monomer Substances 0.000 claims description 14
- -1 ethylidene compound Chemical class 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 11
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 229920002521 macromolecule Polymers 0.000 claims description 3
- NMTZQIYQFZGXQT-UHFFFAOYSA-N C[C]=C Chemical compound C[C]=C NMTZQIYQFZGXQT-UHFFFAOYSA-N 0.000 claims description 2
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 2
- 239000004800 polyvinyl chloride Substances 0.000 claims description 2
- ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical compound C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 description 10
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 3
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- CTRFHBHBZQWUAW-UHFFFAOYSA-N (2,2,2-trichloro-1-prop-2-enoyloxyethyl) prop-2-enoate Chemical compound C=CC(=O)OC(C(Cl)(Cl)Cl)OC(=O)C=C CTRFHBHBZQWUAW-UHFFFAOYSA-N 0.000 description 2
- CARZNHSZGXCIJM-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)OC(=O)C(C)=C CARZNHSZGXCIJM-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- ACKALUBLCWJVNB-UHFFFAOYSA-N ethylidene diacetate Chemical compound CC(=O)OC(C)OC(C)=O ACKALUBLCWJVNB-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- ZXHDFKAHCABVAF-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;methyl 2-methylprop-2-enoate Chemical compound COC(=O)C(C)=C.C=CC1=CC=CC=C1C=C ZXHDFKAHCABVAF-UHFFFAOYSA-N 0.000 description 1
- NKELEXFNIPNREP-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)pentyl 2-methylprop-2-enoate Chemical compound CCCCC(OC(=O)C(C)=C)OC(=O)C(C)=C NKELEXFNIPNREP-UHFFFAOYSA-N 0.000 description 1
- YWOYCXNNAGNDKT-UHFFFAOYSA-N 1-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OC(C)OC(=O)C=C YWOYCXNNAGNDKT-UHFFFAOYSA-N 0.000 description 1
- IHJPMPZEXZSDLU-UHFFFAOYSA-N 1-prop-2-enoyloxypropyl prop-2-enoate Chemical compound C=CC(=O)OC(CC)OC(=O)C=C IHJPMPZEXZSDLU-UHFFFAOYSA-N 0.000 description 1
- FCYVWWWTHPPJII-UHFFFAOYSA-N 2-methylidenepropanedinitrile Chemical compound N#CC(=C)C#N FCYVWWWTHPPJII-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- JBSVNYYKRNVOME-UHFFFAOYSA-N [2,2,2-trichloro-1-(2-methylprop-2-enoyloxy)ethyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C(Cl)(Cl)Cl)OC(=O)C(C)=C JBSVNYYKRNVOME-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- DCUFMVPCXCSVNP-UHFFFAOYSA-N methacrylic anhydride Chemical compound CC(=C)C(=O)OC(=O)C(C)=C DCUFMVPCXCSVNP-UHFFFAOYSA-N 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- SMUVTFSHWISULV-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;prop-2-enenitrile Chemical compound C=CC#N.COC(=O)C(C)=C SMUVTFSHWISULV-UHFFFAOYSA-N 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000001960 triggered effect Effects 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
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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/12—Esters of monohydric alcohols or phenols
-
- 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F20/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
-
- 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
- C08F259/00—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00
- C08F259/02—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00 on to polymers containing chlorine
- C08F259/04—Macromolecular compounds obtained by polymerising monomers on to polymers of halogen containing monomers as defined in group C08F14/00 on to polymers containing chlorine on to polymers of vinyl chloride
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE592804D BE592804A (en:Method) | 1959-07-11 | ||
| DER25925A DE1104700B (de) | 1959-07-11 | 1959-07-11 | Verfahren zur Herstellung von Polymerisationskunststoffen |
| GB24177/60A GB919324A (en) | 1959-07-11 | 1960-07-11 | New synthetic resins |
| FR832637A FR1262338A (fr) | 1959-07-11 | 1960-07-11 | Procédé pour fabriquer des produits de polymérisation |
| DER28731A DE1125177B (de) | 1959-07-11 | 1960-09-13 | Verfahren zur Herstellung von Polymerisationskunststoffen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DER25925A DE1104700B (de) | 1959-07-11 | 1959-07-11 | Verfahren zur Herstellung von Polymerisationskunststoffen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1104700B true DE1104700B (de) | 1961-04-13 |
Family
ID=7402053
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DER25925A Pending DE1104700B (de) | 1959-07-11 | 1959-07-11 | Verfahren zur Herstellung von Polymerisationskunststoffen |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE592804A (en:Method) |
| DE (1) | DE1104700B (en:Method) |
| FR (1) | FR1262338A (en:Method) |
| GB (1) | GB919324A (en:Method) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LT3665B (en) | 1990-09-07 | 1996-01-25 | Nycomed Imaging As | Polymers containing diester units |
| EP0547126B1 (en) * | 1990-09-07 | 1996-02-28 | Nycomed Imaging As | Biodegradable polymers containing diester units |
| US5610226A (en) * | 1994-05-20 | 1997-03-11 | Sumitomo Chemical Company, Limited | (Meth)acrylate copolymer and its elastomer compositions |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL127481C (en:Method) * | 1965-07-07 | 1900-01-01 | ||
| US3459722A (en) * | 1965-10-26 | 1969-08-05 | Murray Zanger | Fluorine-containing polymer |
| US3446761A (en) * | 1965-11-04 | 1969-05-27 | Du Pont | Stain-resistant article,and composition for preparing same |
| JP4691394B2 (ja) * | 2005-05-27 | 2011-06-01 | 出光興産株式会社 | アクリル系化合物、その製造方法及びアクリル系重合体 |
-
0
- BE BE592804D patent/BE592804A/xx unknown
-
1959
- 1959-07-11 DE DER25925A patent/DE1104700B/de active Pending
-
1960
- 1960-07-11 GB GB24177/60A patent/GB919324A/en not_active Expired
- 1960-07-11 FR FR832637A patent/FR1262338A/fr not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LT3665B (en) | 1990-09-07 | 1996-01-25 | Nycomed Imaging As | Polymers containing diester units |
| EP0547126B1 (en) * | 1990-09-07 | 1996-02-28 | Nycomed Imaging As | Biodegradable polymers containing diester units |
| US5534250A (en) * | 1990-09-07 | 1996-07-09 | Nycomed Imaging As | Polymers containing diester units |
| US5610226A (en) * | 1994-05-20 | 1997-03-11 | Sumitomo Chemical Company, Limited | (Meth)acrylate copolymer and its elastomer compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| GB919324A (en) | 1963-02-20 |
| BE592804A (en:Method) | |
| FR1262338A (fr) | 1961-05-26 |
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