DE2441538A1 - Schwerbrennbare terephthalsaeurecopolyester - Google Patents
Schwerbrennbare terephthalsaeurecopolyesterInfo
- Publication number
- DE2441538A1 DE2441538A1 DE19742441538 DE2441538A DE2441538A1 DE 2441538 A1 DE2441538 A1 DE 2441538A1 DE 19742441538 DE19742441538 DE 19742441538 DE 2441538 A DE2441538 A DE 2441538A DE 2441538 A1 DE2441538 A1 DE 2441538A1
- Authority
- DE
- Germany
- Prior art keywords
- radical
- general formula
- terephthalic acid
- carbon atoms
- straight
- 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
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 title claims description 34
- 229920001634 Copolyester Polymers 0.000 title claims description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000003063 flame retardant Substances 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 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 claims description 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 7
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 150000001555 benzenes Chemical class 0.000 claims description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 6
- 239000000155 melt Substances 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 239000000835 fiber Substances 0.000 claims description 5
- 238000006068 polycondensation reaction Methods 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 claims description 4
- 150000002009 diols Chemical class 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 22
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- -1 Polyethylene terephthalate Polymers 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 239000001301 oxygen Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 7
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 description 6
- 239000005020 polyethylene terephthalate Substances 0.000 description 6
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000004246 zinc acetate Substances 0.000 description 5
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 4
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 150000002989 phenols Chemical class 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 3
- DTFQULSULHRJOA-UHFFFAOYSA-N 2,3,5,6-tetrabromobenzene-1,4-diol Chemical compound OC1=C(Br)C(Br)=C(O)C(Br)=C1Br DTFQULSULHRJOA-UHFFFAOYSA-N 0.000 description 2
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 2
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical class C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- JVLRYPRBKSMEBF-UHFFFAOYSA-K diacetyloxystibanyl acetate Chemical compound [Sb+3].CC([O-])=O.CC([O-])=O.CC([O-])=O JVLRYPRBKSMEBF-UHFFFAOYSA-K 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium dioxide Chemical compound O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- YYTSGNJTASLUOY-UHFFFAOYSA-N 1-chloropropan-2-ol Chemical compound CC(O)CCl YYTSGNJTASLUOY-UHFFFAOYSA-N 0.000 description 1
- LWHDQPLUIFIFFT-UHFFFAOYSA-N 2,3,5,6-tetrabromocyclohexa-2,5-diene-1,4-dione Chemical compound BrC1=C(Br)C(=O)C(Br)=C(Br)C1=O LWHDQPLUIFIFFT-UHFFFAOYSA-N 0.000 description 1
- WTPYFJNYAMXZJG-UHFFFAOYSA-N 2-[4-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound OCCOC1=CC=C(OCCO)C=C1 WTPYFJNYAMXZJG-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- OLBVUFHMDRJKTK-UHFFFAOYSA-N [N].[O] Chemical compound [N].[O] OLBVUFHMDRJKTK-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229940119177 germanium dioxide Drugs 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 229940071125 manganese acetate 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
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 102200057142 rs104894430 Human genes 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/672—Dicarboxylic acids and dihydroxy compounds
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/682—Polyesters containing atoms other than carbon, hydrogen and oxygen containing halogens
- C08G63/6824—Polyesters containing atoms other than carbon, hydrogen and oxygen containing halogens derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/6826—Dicarboxylic acids and dihydroxy compounds
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Artificial Filaments (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742441538 DE2441538A1 (de) | 1974-08-30 | 1974-08-30 | Schwerbrennbare terephthalsaeurecopolyester |
| BE159499A BE832788A (fr) | 1974-08-30 | 1975-08-27 | Copolyesters d'acide terephtalique difficilement combustibles |
| NL7510140A NL7510140A (nl) | 1974-08-30 | 1975-08-27 | Moeilijk brandbare tereftaalzuurcopolyesters. |
| LU73268A LU73268A1 (cg-RX-API-DMAC7.html) | 1974-08-30 | 1975-08-28 | |
| DD18806775A DD123890A5 (cg-RX-API-DMAC7.html) | 1974-08-30 | 1975-08-28 | |
| ES440558A ES440558A1 (es) | 1974-08-30 | 1975-08-29 | Procedimiento para la obtencion de copoliesteres de acido teraftalico lineales. |
| GB3570075A GB1513297A (en) | 1974-08-30 | 1975-08-29 | Substantially non-inflammable copolyesters |
| DK390475A DK390475A (da) | 1974-08-30 | 1975-08-29 | Vanskeligt brendbare terephthalsyrecopolyestere samt fremgangsmade til fremstilling heraf |
| JP10416475A JPS5150996A (ja) | 1974-08-30 | 1975-08-29 | Jitsushitsutekinihiinkaseino kohoriesuteru |
| FR7526695A FR2283164A1 (fr) | 1974-08-30 | 1975-08-29 | Copolyesters d'acide terephtalique difficilement combustibles |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742441538 DE2441538A1 (de) | 1974-08-30 | 1974-08-30 | Schwerbrennbare terephthalsaeurecopolyester |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2441538A1 true DE2441538A1 (de) | 1976-03-11 |
Family
ID=5924454
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19742441538 Pending DE2441538A1 (de) | 1974-08-30 | 1974-08-30 | Schwerbrennbare terephthalsaeurecopolyester |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS5150996A (cg-RX-API-DMAC7.html) |
| BE (1) | BE832788A (cg-RX-API-DMAC7.html) |
| DD (1) | DD123890A5 (cg-RX-API-DMAC7.html) |
| DE (1) | DE2441538A1 (cg-RX-API-DMAC7.html) |
| DK (1) | DK390475A (cg-RX-API-DMAC7.html) |
| ES (1) | ES440558A1 (cg-RX-API-DMAC7.html) |
| FR (1) | FR2283164A1 (cg-RX-API-DMAC7.html) |
| GB (1) | GB1513297A (cg-RX-API-DMAC7.html) |
| LU (1) | LU73268A1 (cg-RX-API-DMAC7.html) |
| NL (1) | NL7510140A (cg-RX-API-DMAC7.html) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3030988A1 (de) * | 1980-08-16 | 1982-03-18 | Chemische Fabrik Kalk GmbH, 5000 Köln | Polytetrabromphenylenterephthalat, seine herstellung und anwendung |
| EP0283237A3 (en) * | 1987-03-16 | 1989-07-26 | Polyplastics Co. Ltd. | Halogen-containing polyester resin composition and electric wire coated therewith |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4469834A (en) * | 1983-05-11 | 1984-09-04 | Celanese Corporation | Poly(butylene terephthalate) based molding resins |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3887523A (en) * | 1974-06-24 | 1975-06-03 | Emery Industries Inc | Fiber-forming copolyester compositions from brominated ethoxylated hydroquinone |
-
1974
- 1974-08-30 DE DE19742441538 patent/DE2441538A1/de active Pending
-
1975
- 1975-08-27 NL NL7510140A patent/NL7510140A/xx not_active Application Discontinuation
- 1975-08-27 BE BE159499A patent/BE832788A/xx unknown
- 1975-08-28 DD DD18806775A patent/DD123890A5/xx unknown
- 1975-08-28 LU LU73268A patent/LU73268A1/xx unknown
- 1975-08-29 JP JP10416475A patent/JPS5150996A/ja active Pending
- 1975-08-29 FR FR7526695A patent/FR2283164A1/fr active Granted
- 1975-08-29 GB GB3570075A patent/GB1513297A/en not_active Expired
- 1975-08-29 DK DK390475A patent/DK390475A/da unknown
- 1975-08-29 ES ES440558A patent/ES440558A1/es not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3030988A1 (de) * | 1980-08-16 | 1982-03-18 | Chemische Fabrik Kalk GmbH, 5000 Köln | Polytetrabromphenylenterephthalat, seine herstellung und anwendung |
| EP0283237A3 (en) * | 1987-03-16 | 1989-07-26 | Polyplastics Co. Ltd. | Halogen-containing polyester resin composition and electric wire coated therewith |
Also Published As
| Publication number | Publication date |
|---|---|
| BE832788A (fr) | 1976-02-27 |
| ES440558A1 (es) | 1977-03-01 |
| JPS5150996A (ja) | 1976-05-06 |
| GB1513297A (en) | 1978-06-07 |
| NL7510140A (nl) | 1976-03-02 |
| LU73268A1 (cg-RX-API-DMAC7.html) | 1976-05-31 |
| DK390475A (da) | 1976-03-01 |
| FR2283164A1 (fr) | 1976-03-26 |
| DD123890A5 (cg-RX-API-DMAC7.html) | 1977-01-19 |
| FR2283164B1 (cg-RX-API-DMAC7.html) | 1979-05-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2645711C3 (de) | Halogenhaltige Flammschutzmittel enthaltende Fasern und Fäden aus linearen, thermoplastischen Polyestern | |
| DE3139127A1 (de) | Copolyester mit verbesserter anfaerbbarkeit | |
| DE3751211T2 (de) | In-situ Blockierung mit Endgruppen von in der Schmelze hergestellten aromatischen Polyestern zur Produktion von Polymeren mit verbesserter Stabilität. | |
| DE2313298A1 (de) | Flammverzoegernder faserbildender copolyester | |
| DE1720235A1 (de) | Neue Copolyester,ihre Herstellung und Verwendung | |
| DE1243819B (de) | Verwendung phosphorhaltiger Polyester zum Herstellen von Faeden oder Fasern | |
| EP0374657A2 (de) | Neue thermotrope Polyester, Verfahren zu ihrer Herstellung sowie ihre Verwendung zur Herstellung von Formkörpern, Filamenten, Fasern und Folien | |
| DE2113859A1 (de) | Faserbildende Polyestermasse,Polyesterfasern und Verfahren zu deren Herstellung | |
| DE2545720A1 (de) | Schnellkristallisierende blockcopolyester | |
| DE2441538A1 (de) | Schwerbrennbare terephthalsaeurecopolyester | |
| DE2746338A1 (de) | Feuerfeste copolyester mit phosphongruppen | |
| CH515287A (de) | Verfahren zur Herstellung von Copolyestern | |
| DE2311849C3 (de) | Verfahren zur Herstellung von segmentierten, thermoplastischen, elastomeren Mischpolyestern | |
| DE4328800A1 (de) | Pillarm und schwer entflammbar modifizierte Polyester, Verfahren zu ihrer Herstellung und daraus geformte Gebilde | |
| DE60225568T2 (de) | Polytrimethylenterephthalat-polyester | |
| EP1917287B1 (de) | Polyester von terephthalsäure, ein verfahren zu deren herstellung und deren verwendung | |
| DE1254285B (de) | Phosphorsaeure-modifizierte Mischpolyester zum Herstellen von Faeden nach dem Schmelzspinnverfahren | |
| DE4334492A1 (de) | Pillarme und schwer entflammbare, Phosphor und Silizium enthaltende Polyester-Mischungen, Verfahren zu ihrer Herstellung und daraus geformte Gebilde | |
| AT264140B (de) | Verfahren zur Herstellung 2,5-Dihydroxyterephthalsäure enthaltender Polyester und Copolyester | |
| DE2755640A1 (de) | Verfahren zur herstellung von polyesterharzen mit stabilisierter schmelzviskositaet in gegenwart eines aromatischen carbonats oder polycarbonats | |
| DE2105928A1 (de) | Lineare Polyatherester, Verfahren zu derer. Herstellung und hieraus ge formte Gegen Stande | |
| EP0284726A2 (de) | Aromatische Polyester auf Basis von Phenoxyterephthalsäure, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE69131415T2 (de) | Polyesterfaser | |
| DE2324349A1 (de) | Lichtstabilisierte synthetische lineare polyester sowie geformte gebilde daraus | |
| DE1570951B2 (de) | Verfahren zur Herstellung von Mischpolyestern |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OHN | Withdrawal |