PL63817B1 - - Google Patents
Download PDFInfo
- Publication number
- PL63817B1 PL63817B1 PL120392A PL12039267A PL63817B1 PL 63817 B1 PL63817 B1 PL 63817B1 PL 120392 A PL120392 A PL 120392A PL 12039267 A PL12039267 A PL 12039267A PL 63817 B1 PL63817 B1 PL 63817B1
- Authority
- PL
- Poland
- Prior art keywords
- catalyst
- sodium
- amount
- stabilizer
- potassium
- Prior art date
Links
- 238000000034 method Methods 0.000 claims description 33
- 239000003054 catalyst Substances 0.000 claims description 21
- 229920000515 polycarbonate Polymers 0.000 claims description 13
- 239000004417 polycarbonate Substances 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 10
- -1 dihydrate compound Chemical class 0.000 claims description 9
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 8
- 229910052700 potassium Inorganic materials 0.000 claims description 8
- 239000011591 potassium Substances 0.000 claims description 8
- 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 claims description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 239000011734 sodium Substances 0.000 claims description 7
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 6
- 150000001340 alkali metals Chemical class 0.000 claims description 6
- 229910052744 lithium Inorganic materials 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 229910052701 rubidium Inorganic materials 0.000 claims description 5
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 claims description 5
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 4
- 239000004327 boric acid Substances 0.000 claims description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims description 2
- 229910001515 alkali metal fluoride Inorganic materials 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims 6
- 150000001491 aromatic compounds Chemical class 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- VNWHJJCHHGPAEO-UHFFFAOYSA-N fluoroboronic acid Chemical class OB(O)F VNWHJJCHHGPAEO-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 7
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 5
- JLAVCPKULITDHO-UHFFFAOYSA-N tetraphenylsilane Chemical compound C1=CC=CC=C1[Si](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 JLAVCPKULITDHO-UHFFFAOYSA-N 0.000 description 5
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 4
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 235000013024 sodium fluoride Nutrition 0.000 description 2
- 239000011775 sodium fluoride Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- QGBLCIBATKETJC-UHFFFAOYSA-N 3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane;manganese(2+) Chemical compound [Mn+2].O1B([O-])OB2OB([O-])OB1O2 QGBLCIBATKETJC-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 150000008043 acidic salts Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 229910000102 alkali metal hydride Inorganic materials 0.000 description 1
- 150000008046 alkali metal hydrides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 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 1
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical class OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000002696 manganese Chemical class 0.000 description 1
- 229940071125 manganese acetate Drugs 0.000 description 1
- 235000006748 manganese carbonate Nutrition 0.000 description 1
- 239000011656 manganese carbonate Substances 0.000 description 1
- 229940093474 manganese carbonate Drugs 0.000 description 1
- UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 description 1
- HDJUVFZHZGPHCQ-UHFFFAOYSA-L manganese(2+);oxalate;dihydrate Chemical compound O.O.[Mn+2].[O-]C(=O)C([O-])=O HDJUVFZHZGPHCQ-UHFFFAOYSA-L 0.000 description 1
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 description 1
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- KVGSJGNWRDPVKA-UHFFFAOYSA-N quinoline-5-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=N1 KVGSJGNWRDPVKA-UHFFFAOYSA-N 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE714612D BE714612A (en:Method) | 1967-05-05 | 1968-05-03 | |
GB21052/68A GB1217349A (en) | 1967-05-05 | 1968-05-03 | Process for the production of carbonic acid polyesters |
DE19681770329 DE1770329A1 (de) | 1967-05-05 | 1968-05-03 | Verfahren zur Herstellung von Polycarbonaten |
US726544A US3625920A (en) | 1967-05-05 | 1968-05-03 | Process for the production of carbonic acid polyesters |
FR1578918D FR1578918A (en:Method) | 1967-05-05 | 1968-05-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
PL63817B1 true PL63817B1 (en:Method) | 1971-08-31 |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3022272A (en) | Process for the production of high | |
KR920003711B1 (ko) | 결정화 방향족 폴리카르보네이트의 제조방법과 이에 의하여 얻어지는 결정화 방향족 폴리카르보네이트 | |
JP2003321540A (ja) | 高分子量の脂肪族ポリカーボネート、その製造方法およびそれを含有する成形物品 | |
US3312659A (en) | Catalytic preparation of polycarbon- ates from bisphenol and a carbonate precursor | |
ITMI931235A1 (it) | Processo per la scissione di policarbonati in bisfenoli e diarilcarbonati | |
US3234263A (en) | Process for preparing diaryl carbonates | |
KR20200010230A (ko) | 방향족 폴리카보네이트 올리고머 고형체 | |
PL63817B1 (en:Method) | ||
EP0002218B1 (de) | Verfahren zur Herstellung aromatischer Polyester | |
US4650852A (en) | Method for controlling polymerization rate of cyclic polycarbonate oligomers with pretreated catalyst | |
US5434235A (en) | Process for the preparation of (co)polycarbonate | |
KR101161031B1 (ko) | 폴리카보네이트 생산 방법 | |
US4225483A (en) | Boric acid esters and oxetanes for stabilizing phosphite-free polycarbonates | |
KR20200010233A (ko) | 방향족 폴리카보네이트 올리고머 고형체 | |
JPH02180925A (ja) | 芳香族ポリカーボネートの製造法 | |
TW201734093A (zh) | 芳香族聚碸樹脂及其製造方法 | |
US5314985A (en) | Molten, catalytic process for the preparation of polycarbonates | |
JPH06271659A (ja) | 結晶性芳香族ポリカーボネートプレポリマーの製造方法及び芳香族ポリカーボネートの製造方法 | |
EP0207292B1 (en) | Method for preparing bischloroformate compositions | |
KR100707332B1 (ko) | 폴리카르보네이트의 제조 방법 | |
JPH1060106A (ja) | ポリカーボネートの製造方法 | |
JPH0662759B2 (ja) | 金属キレート触媒を使用して環状オリゴマー組成物から線状ポリカーボネートを製造する方法 | |
US3234261A (en) | Process for preparing diaryl carbonates | |
US3321439A (en) | Phosphoric acid diaryl esters as catalysts in transesterification of diarylcarbonates with dihydric phenols | |
EP0224769B1 (en) | Crosslinkable polycyclic polycarbonate oligomers and methods for their preparation |