DE2829256A1 - Polycarbonate mit uv-licht-vernetzbaren doppelbindungen enthaltenden endgruppen - Google Patents
Polycarbonate mit uv-licht-vernetzbaren doppelbindungen enthaltenden endgruppenInfo
- Publication number
- DE2829256A1 DE2829256A1 DE19782829256 DE2829256A DE2829256A1 DE 2829256 A1 DE2829256 A1 DE 2829256A1 DE 19782829256 DE19782829256 DE 19782829256 DE 2829256 A DE2829256 A DE 2829256A DE 2829256 A1 DE2829256 A1 DE 2829256A1
- Authority
- DE
- Germany
- Prior art keywords
- polycarbonates
- polycarbonate
- formula
- weight
- diphenols
- 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.)
- Withdrawn
Links
- 229920000515 polycarbonate Polymers 0.000 title claims description 59
- 239000004417 polycarbonate Substances 0.000 title claims description 59
- 238000000034 method Methods 0.000 claims description 15
- -1 aromatic dihydroxy ketones Chemical class 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 239000003063 flame retardant Substances 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 2
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 10
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000005336 cracking Methods 0.000 description 5
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 239000012074 organic phase Substances 0.000 description 4
- SNGREZUHAYWORS-UHFFFAOYSA-N perfluorooctanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SNGREZUHAYWORS-UHFFFAOYSA-N 0.000 description 4
- LVTHXRLARFLXNR-UHFFFAOYSA-M potassium;1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate Chemical compound [K+].[O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F LVTHXRLARFLXNR-UHFFFAOYSA-M 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- VHRYZQNGTZXDNX-UHFFFAOYSA-N methacryloyl chloride Chemical compound CC(=C)C(Cl)=O VHRYZQNGTZXDNX-UHFFFAOYSA-N 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- NXXYKOUNUYWIHA-UHFFFAOYSA-N 2,6-Dimethylphenol Chemical compound CC1=CC=CC(C)=C1O NXXYKOUNUYWIHA-UHFFFAOYSA-N 0.000 description 2
- RXNYJUSEXLAVNQ-UHFFFAOYSA-N 4,4'-Dihydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=C(O)C=C1 RXNYJUSEXLAVNQ-UHFFFAOYSA-N 0.000 description 2
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 150000007530 organic bases Chemical class 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920000642 polymer Polymers 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
- 230000001105 regulatory effect Effects 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 229910052701 rubidium Inorganic materials 0.000 description 2
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Chemical class CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 1
- VXHYVVAUHMGCEX-UHFFFAOYSA-N 2-(2-hydroxyphenoxy)phenol Chemical class OC1=CC=CC=C1OC1=CC=CC=C1O VXHYVVAUHMGCEX-UHFFFAOYSA-N 0.000 description 1
- BLDLRWQLBOJPEB-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfanylphenol Chemical class OC1=CC=CC=C1SC1=CC=CC=C1O BLDLRWQLBOJPEB-UHFFFAOYSA-N 0.000 description 1
- XSVZEASGNTZBRQ-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfinylphenol Chemical class OC1=CC=CC=C1S(=O)C1=CC=CC=C1O XSVZEASGNTZBRQ-UHFFFAOYSA-N 0.000 description 1
- QUWAJPZDCZDTJS-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfonylphenol Chemical class OC1=CC=CC=C1S(=O)(=O)C1=CC=CC=C1O QUWAJPZDCZDTJS-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Chemical class CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Chemical class CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Chemical class 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Chemical class CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- KYPYTERUKNKOLP-UHFFFAOYSA-N Tetrachlorobisphenol A Chemical compound C=1C(Cl)=C(O)C(Cl)=CC=1C(C)(C)C1=CC(Cl)=C(O)C(Cl)=C1 KYPYTERUKNKOLP-UHFFFAOYSA-N 0.000 description 1
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052736 halogen Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Chemical class CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- XIKIUQUXDNHBFR-UHFFFAOYSA-N monobenzyl phthalate Chemical class OC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 XIKIUQUXDNHBFR-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical class CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- WFRUBUQWJYMMRQ-UHFFFAOYSA-M potassium;1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonate Chemical compound [K+].[O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F WFRUBUQWJYMMRQ-UHFFFAOYSA-M 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000008117 stearic acid Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 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
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/28—Treatment by wave energy or particle radiation
-
- 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
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/04—Aromatic polycarbonates
- C08G64/045—Aromatic polycarbonates containing aliphatic unsaturation
-
- 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)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782829256 DE2829256A1 (de) | 1978-07-04 | 1978-07-04 | Polycarbonate mit uv-licht-vernetzbaren doppelbindungen enthaltenden endgruppen |
| DE7979102050T DE2961541D1 (en) | 1978-07-04 | 1979-06-21 | Polycarbonates with double bonds cross-linkable by uv light, process for preparing same, process for their modification and the products obtained thereby |
| US06/050,899 US4221645A (en) | 1978-07-04 | 1979-06-21 | Polycarbonates with end groups containing double bonds which can be crosslinked by UV light |
| EP79102050A EP0006579B1 (de) | 1978-07-04 | 1979-06-21 | Polycarbonate mit UV-Licht-vernetzbaren Doppelbindungen, Verfahren zu ihrer Herstellung, Verfahren zu ihrer Modifizierung sowie die hierbei erhaltenen Produkte |
| JP8273779A JPS559696A (en) | 1978-07-04 | 1979-07-02 | Polycarbonate having end group with uv light crosslinkable double bond |
| JP62033560A JPS62246929A (ja) | 1978-07-04 | 1987-02-18 | ポリカ−ボネ−トの改質法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782829256 DE2829256A1 (de) | 1978-07-04 | 1978-07-04 | Polycarbonate mit uv-licht-vernetzbaren doppelbindungen enthaltenden endgruppen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2829256A1 true DE2829256A1 (de) | 1980-01-17 |
Family
ID=6043467
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19782829256 Withdrawn DE2829256A1 (de) | 1978-07-04 | 1978-07-04 | Polycarbonate mit uv-licht-vernetzbaren doppelbindungen enthaltenden endgruppen |
| DE7979102050T Expired DE2961541D1 (en) | 1978-07-04 | 1979-06-21 | Polycarbonates with double bonds cross-linkable by uv light, process for preparing same, process for their modification and the products obtained thereby |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE7979102050T Expired DE2961541D1 (en) | 1978-07-04 | 1979-06-21 | Polycarbonates with double bonds cross-linkable by uv light, process for preparing same, process for their modification and the products obtained thereby |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4221645A (en:Method) |
| EP (1) | EP0006579B1 (en:Method) |
| JP (2) | JPS559696A (en:Method) |
| DE (2) | DE2829256A1 (en:Method) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4333809A (en) | 1979-07-28 | 1982-06-08 | Bayer Aktiengesellschaft | Cross-linkable polycarbonate elastomers, a process for their preparation and use for packaging medicines |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3232391A1 (de) * | 1982-08-31 | 1984-03-01 | Bayer Ag, 5090 Leverkusen | Polycarbonate mit konjugierte doppelbindungen enthaltenden endgruppen, gegebenenfalls im gemisch mit bekannten aromatischen polycarbonaten, ihre herstellung und ihre verwendung |
| DE3609616A1 (de) * | 1986-03-21 | 1988-01-07 | Ciba Geigy Ag | Verfahren zur herstellung eines spannungsriss- und temperaturbestaendigen kunststoffs |
| DE3803939A1 (de) * | 1988-02-10 | 1989-08-24 | Bayer Ag | Polycarbonate mit aralkylphenylendgruppen, ihre herstellung und verwendung |
| US5171824A (en) * | 1990-12-24 | 1992-12-15 | The Dow Chemical Company | Process for the preparation of arylcyclobutene terminated condensation polymers |
| US5198527A (en) * | 1990-12-24 | 1993-03-30 | The Dow Chemical Company | Arylcyclobutene terminated carbonate polymer |
| EP0531920B1 (en) * | 1991-09-12 | 2000-02-09 | Mitsubishi Gas Chemical Company, Inc. | Polycarbonate resins having terminal vinyl groups and process for producing the same |
| JP3097934B2 (ja) * | 1991-12-13 | 2000-10-10 | 日本ジーイープラスチックス株式会社 | 艶消し熱可塑性樹脂組成物 |
| US5679721A (en) * | 1995-02-27 | 1997-10-21 | Domco Industries Ltd. | Curable coating composition for sheet goods |
| EP0866083B1 (en) * | 1995-12-04 | 2003-05-28 | Idemitsu Kosan Company Limited | Polycarbonate resin, crosslinked polycarbonate resin and electrophotographic photoreceptor |
| JP5601359B2 (ja) * | 2012-09-28 | 2014-10-08 | 三菱エンジニアリングプラスチックス株式会社 | 芳香族ポリカーボネート樹脂粉粒体の製造方法及び樹脂成形体 |
| CN104937009B (zh) * | 2012-12-20 | 2017-12-08 | 沙特基础全球技术有限公司 | 包含光活性添加剂的共混物 |
| EP2935396A1 (en) | 2012-12-20 | 2015-10-28 | SABIC Global Technologies B.V. | Cross-linked polycarbonate resin with improved chemical and flame resistance |
| CN105073830A (zh) * | 2013-03-13 | 2015-11-18 | 沙特基础全球技术有限公司 | 具有改善的耐化学性和阻燃性的多官能光活性添加剂 |
| US9110370B2 (en) | 2013-03-14 | 2015-08-18 | Sabic Global Technologies B.V. | Photoactive additive with functionalized benzophenone |
| EP2970655B1 (en) * | 2013-03-15 | 2021-10-27 | SHPP Global Technologies B.V. | Blends containing photoactive additive |
| CN105051090B (zh) | 2013-03-15 | 2017-06-16 | 沙特基础全球技术有限公司 | 用于制备光活性添加剂的界面方法 |
| WO2014144673A1 (en) | 2013-03-15 | 2014-09-18 | Sabic Innovative Plastics Ip B.V. | Photoactive additives containing siloxane |
| EP2970578A1 (en) * | 2013-03-15 | 2016-01-20 | SABIC Global Technologies B.V. | Processes for enhancing flame retardance and chemical resistance of polymers |
| WO2015193859A1 (en) | 2014-06-19 | 2015-12-23 | Sabic Global Technologies B.V. | Brominated cross-linkable polycarbonate compositions |
| DE202015009117U1 (de) | 2014-06-20 | 2016-10-24 | Google Inc. | Integration von Online-Navigationsdaten mit gecachten Navigationsdaten während der aktiven Navigation |
| JP2017518424A (ja) | 2014-06-20 | 2017-07-06 | サビック グローバル テクノロジーズ ベスローテン フェンノートシャップ | 架橋性ポリカーボネートのための溶融反応法 |
| EP3157979A1 (en) * | 2014-06-20 | 2017-04-26 | SABIC Global Technologies B.V. | Processes for designing cross-linkable polycarbonates and articles formed therefrom |
| WO2016044218A1 (en) | 2014-09-17 | 2016-03-24 | Sabic Global Technologies B.V. | Colored cross-linkable polycarbonate compositions |
| CN109232839B (zh) * | 2018-08-06 | 2021-04-06 | 浙江工业大学 | 一种具有光响应的3d打印可降解材料及其制备方法 |
| CN113646359B (zh) | 2019-04-02 | 2023-05-02 | 三菱瓦斯化学株式会社 | 聚碳酸酯树脂 |
| JP7605109B2 (ja) * | 2019-06-10 | 2024-12-24 | 三菱瓦斯化学株式会社 | ポリカーボネート樹脂 |
| CN112430316B (zh) * | 2020-11-23 | 2022-05-13 | 青岛展辰新材料有限公司 | 聚碳酸酯光引发剂的制备方法及其应用 |
| CN114276241A (zh) * | 2021-11-17 | 2022-04-05 | 南昌航空大学 | 一种双官能团可聚合肉桂酰改性二苯甲酮光引发剂及其制备方法 |
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| US3124555A (en) * | 1964-03-10 | Table i | ||
| US2838474A (en) * | 1954-01-28 | 1958-06-10 | Ruetgerswerke Ag | Condensation products of bisphenols with aromatic vinyl compounds |
| US3150066A (en) * | 1958-07-02 | 1964-09-22 | Bayer Ag | Process for the alteration of the physical and chemical properties of polycarbonates |
| NL240570A (en:Method) | 1958-07-02 | |||
| DE1099732B (de) | 1958-08-18 | 1961-02-16 | Bayer Ag | Verfahren zur Herstellung von unter Einwirkung von aktinischem Licht vernetzenden, schwer- bzw. unloeslich werdenden Polycarbonaten mit -CH=CH-CO-Gruppen |
| US3453237A (en) * | 1959-07-21 | 1969-07-01 | Eastman Kodak Co | Light-sensitive polymers having a linear chain containing the styryl ketone group |
| US3518175A (en) * | 1965-05-12 | 1970-06-30 | Du Pont | Process of forming crosslinkable copolymers of polyesters and substituted benzophenones and product thereof |
| US3475373A (en) * | 1965-08-11 | 1969-10-28 | Eastman Kodak Co | Stabilization of polycarbonates |
| US3600288A (en) * | 1969-01-03 | 1971-08-17 | Gen Electric | Curable silicone-polycarbonate copolymer composition |
| AT297333B (de) * | 1969-06-13 | 1972-03-27 | Bayer Ag | Verfahren zur Herstellung von Polycarbonaten mit verminderter Brennbarkeit |
| US3622331A (en) * | 1969-06-23 | 1971-11-23 | Lithoplate Inc | Polycarbonate-cinnamate photopolymer |
| US3787302A (en) * | 1970-10-19 | 1974-01-22 | Nitto Electric Ind Co | Photo-sensitive cross-linking agents for high molecular weight materials |
| US3789052A (en) * | 1971-04-30 | 1974-01-29 | Gen Electric | Imido-alkylene substituted aromatic carbocyclic polymers |
| US4028204A (en) * | 1971-11-18 | 1977-06-07 | Sun Chemical Corporation | Photopolymerizable compounds and compositions comprising the product of the reaction of a resin and a polycarboxy-substituted benzophenone |
| DE2211641C3 (de) * | 1972-03-10 | 1975-08-21 | Bayer Ag, 5090 Leverkusen | Verfahren zur Stabilisierung von Formteilen aus hochmolekularen thermoplastischen Polycarbonaten |
| JPS4999596A (en:Method) * | 1973-01-25 | 1974-09-20 | ||
| CA1036744A (en) * | 1973-03-30 | 1978-08-15 | Heinrich Haupt | Process for preparing halogen-substituted aromatic polycarbonates |
| US3992276A (en) * | 1975-03-17 | 1976-11-16 | Celanese Corporation | Unsaturated polyesters for ultraviolet curable coatings |
| US4101399A (en) * | 1976-03-08 | 1978-07-18 | Celanese Corporation | Production of solvent resistant brominated and/or chlorinated aromatic polyester fibrous materials |
| DE2615038C3 (de) * | 1976-04-07 | 1980-08-21 | Bayer Ag, 5090 Leverkusen | l,lA4,6-Pentamethyl-3-(3^-dimethyl-4-hydroxyphenyl)- indan-5-ol - Polycarbonate |
| GB1544788A (en) * | 1976-05-07 | 1979-04-25 | Bayer Ag | Process for the preparation of polycarbonate mixtures |
| FR2375271A1 (fr) * | 1976-12-23 | 1978-07-21 | Poudres & Explosifs Ste Nale | Nouveaux polycarbonates a terminaisons acryliques ou methacryliques et leurs applications a la photoreticulation |
| JPS6233559A (ja) * | 1985-08-02 | 1987-02-13 | 極東開発工業株式会社 | 破袋機 |
-
1978
- 1978-07-04 DE DE19782829256 patent/DE2829256A1/de not_active Withdrawn
-
1979
- 1979-06-21 DE DE7979102050T patent/DE2961541D1/de not_active Expired
- 1979-06-21 EP EP79102050A patent/EP0006579B1/de not_active Expired
- 1979-06-21 US US06/050,899 patent/US4221645A/en not_active Expired - Lifetime
- 1979-07-02 JP JP8273779A patent/JPS559696A/ja active Granted
-
1987
- 1987-02-18 JP JP62033560A patent/JPS62246929A/ja active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4333809A (en) | 1979-07-28 | 1982-06-08 | Bayer Aktiengesellschaft | Cross-linkable polycarbonate elastomers, a process for their preparation and use for packaging medicines |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0006579A1 (de) | 1980-01-09 |
| JPH0449567B2 (en:Method) | 1992-08-11 |
| JPS559696A (en) | 1980-01-23 |
| JPS62246929A (ja) | 1987-10-28 |
| DE2961541D1 (en) | 1982-02-04 |
| EP0006579B1 (de) | 1981-12-09 |
| US4221645A (en) | 1980-09-09 |
| JPS6249297B2 (en:Method) | 1987-10-19 |
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