DD145756A5 - Verfahren zur herstellung von copoly(karbonat/phosphonat)zusammensetzungen - Google Patents

Verfahren zur herstellung von copoly(karbonat/phosphonat)zusammensetzungen Download PDF

Info

Publication number: DD145756A5
Authority: DD; German Democratic Republic
Prior art keywords: item; crosslinking agent; carbonate; chain; phosphonate
Prior art date: 1978-08-11

Application number

DD79214894A

Other languages

German (de)

English (en)

Inventor

Siegfried Altscher

Arthur J Yu

Original Assignee

Stauffer Chemical Co

Priority date (The priority date 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 date listed.)

1978-08-11

Filing date

1979-08-09

Publication date

1981-01-07

1979-08-09 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1981-01-07 Publication of DD145756A5 publication Critical patent/DD145756A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 46
229920001577 copolymer Chemical compound 0.000 title claims abstract description 35
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 title claims abstract description 28
238000004519 manufacturing process Methods 0.000 title claims abstract description 9
239000003431 cross linking reagent Substances 0.000 claims abstract description 25
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 18
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 17
239000002243 precursor Substances 0.000 claims abstract description 12
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims description 33
238000000034 method Methods 0.000 claims description 18
239000003795 chemical substances by application Substances 0.000 claims description 9
WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 claims description 6
150000001875 compounds Chemical class 0.000 claims description 5
229910052698 phosphorus Inorganic materials 0.000 claims description 5
239000011574 phosphorus Substances 0.000 claims description 5
238000001879 gelation Methods 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
229910052794 bromium Chemical group 0.000 claims description 3
239000000460 chlorine Substances 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
-1 phosphorus compound Chemical class 0.000 claims description 3
229940079877 pyrogallol Drugs 0.000 claims description 3
JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
125000001309 chloro group Chemical group Cl* 0.000 claims description 2
QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 claims description 2
229960001553 phloroglucinol Drugs 0.000 claims description 2
235000015250 liver sausages Nutrition 0.000 claims 1
238000002844 melting Methods 0.000 abstract description 20
230000008018 melting Effects 0.000 abstract description 20
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 93
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 68
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 39
239000000047 product Substances 0.000 description 33
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 22
238000006243 chemical reaction Methods 0.000 description 17
239000004033 plastic Substances 0.000 description 14
229920003023 plastic Polymers 0.000 description 14
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 13
YBTMSVKMINMVAZ-UHFFFAOYSA-N pocl3 benzene Chemical compound ClP(Cl)(Cl)=O.C1=CC=CC=C1 YBTMSVKMINMVAZ-UHFFFAOYSA-N 0.000 description 12
229930185605 Bisphenol Natural products 0.000 description 9
238000002360 preparation method Methods 0.000 description 9
QUWAJPZDCZDTJS-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfonylphenol Chemical compound OC1=CC=CC=C1S(=O)(=O)C1=CC=CC=C1O QUWAJPZDCZDTJS-UHFFFAOYSA-N 0.000 description 8
230000015572 biosynthetic process Effects 0.000 description 8
RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 8
238000002474 experimental method Methods 0.000 description 7
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 6
QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
150000002989 phenols Chemical class 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
238000003786 synthesis reaction Methods 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
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 4
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
239000012467 final product Substances 0.000 description 4
239000003063 flame retardant Substances 0.000 description 4
239000004417 polycarbonate Substances 0.000 description 4
229920000515 polycarbonate Polymers 0.000 description 4
239000004431 polycarbonate resin Substances 0.000 description 4
229920005668 polycarbonate resin Polymers 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
KHKQVDWJVRSYOG-UHFFFAOYSA-N C[ClH]P(=O)(Cl)Cl Chemical compound C[ClH]P(=O)(Cl)Cl KHKQVDWJVRSYOG-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical group OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 3
239000000178 monomer Substances 0.000 description 3
230000008569 process Effects 0.000 description 3
239000000376 reactant Substances 0.000 description 3
XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 2
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-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
239000002253 acid Substances 0.000 description 2
PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
230000006835 compression Effects 0.000 description 2
238000007906 compression Methods 0.000 description 2
150000005205 dihydroxybenzenes Chemical class 0.000 description 2
230000009477 glass transition Effects 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
239000012429 reaction media Substances 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000012815 thermoplastic material Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
AYNPIRVEWMUJDE-UHFFFAOYSA-N 2,5-dichlorohydroquinone Chemical compound OC1=CC(Cl)=C(O)C=C1Cl AYNPIRVEWMUJDE-UHFFFAOYSA-N 0.000 description 1
ZKZKMLKTQUCSNX-UHFFFAOYSA-N 2,6-dibromo-4-(3,5-dibromo-4-hydroxyphenyl)sulfinylphenol Chemical compound C1=C(Br)C(O)=C(Br)C=C1S(=O)C1=CC(Br)=C(O)C(Br)=C1 ZKZKMLKTQUCSNX-UHFFFAOYSA-N 0.000 description 1
TXYQFJWVHVYIHB-UHFFFAOYSA-N 2,6-dichloro-4-(3,5-dichloro-4-hydroxyphenoxy)phenol Chemical compound C1=C(Cl)C(O)=C(Cl)C=C1OC1=CC(Cl)=C(O)C(Cl)=C1 TXYQFJWVHVYIHB-UHFFFAOYSA-N 0.000 description 1
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound 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 1
YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 description 1
HCDMJFOHIXMBOV-UHFFFAOYSA-N 3-(2,6-difluoro-3,5-dimethoxyphenyl)-1-ethyl-8-(morpholin-4-ylmethyl)-4,7-dihydropyrrolo[4,5]pyrido[1,2-d]pyrimidin-2-one Chemical compound C=1C2=C3N(CC)C(=O)N(C=4C(=C(OC)C=C(OC)C=4F)F)CC3=CN=C2NC=1CN1CCOCC1 HCDMJFOHIXMBOV-UHFFFAOYSA-N 0.000 description 1
VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 description 1
MLDIQALUMKMHCC-UHFFFAOYSA-N 4,4-Bis(4-hydroxyphenyl)heptane Chemical compound C=1C=C(O)C=CC=1C(CCC)(CCC)C1=CC=C(O)C=C1 MLDIQALUMKMHCC-UHFFFAOYSA-N 0.000 description 1
SUCTVKDVODFXFX-UHFFFAOYSA-N 4-(4-hydroxy-3,5-dimethylphenyl)sulfonyl-2,6-dimethylphenol Chemical compound CC1=C(O)C(C)=CC(S(=O)(=O)C=2C=C(C)C(O)=C(C)C=2)=C1 SUCTVKDVODFXFX-UHFFFAOYSA-N 0.000 description 1
NZGQHKSLKRFZFL-UHFFFAOYSA-N 4-(4-hydroxyphenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(O)C=C1 NZGQHKSLKRFZFL-UHFFFAOYSA-N 0.000 description 1
RQCACQIALULDSK-UHFFFAOYSA-N 4-(4-hydroxyphenyl)sulfinylphenol Chemical compound C1=CC(O)=CC=C1S(=O)C1=CC=C(O)C=C1 RQCACQIALULDSK-UHFFFAOYSA-N 0.000 description 1
GZFGOTFRPZRKDS-UHFFFAOYSA-N 4-bromophenol Chemical compound OC1=CC=C(Br)C=C1 GZFGOTFRPZRKDS-UHFFFAOYSA-N 0.000 description 1
206010000234 Abortion spontaneous Diseases 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
239000004971 Cross linker Substances 0.000 description 1
229910019213 POCl3 Inorganic materials 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
230000009471 action Effects 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
MOIPGXQKZSZOQX-UHFFFAOYSA-N carbonyl bromide Chemical compound BrC(Br)=O MOIPGXQKZSZOQX-UHFFFAOYSA-N 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
229930003836 cresol Natural products 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000003999 initiator Substances 0.000 description 1
229940050176 methyl chloride Drugs 0.000 description 1
208000015994 miscarriage Diseases 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
230000006855 networking Effects 0.000 description 1
238000005580 one pot reaction Methods 0.000 description 1
239000003960 organic solvent 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
150000003018 phosphorus compounds Chemical class 0.000 description 1
238000012643 polycondensation polymerization Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000003825 pressing Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
208000000995 spontaneous abortion Diseases 0.000 description 1
150000003462 sulfoxides Chemical class 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
150000003739 xylenols Chemical class 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
- C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
- C08G79/02—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule a linkage containing phosphorus
- C08G79/04—Phosphorus linked to oxygen or to oxygen and carbon
- 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

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)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

DD79214894A 1978-08-11 1979-08-09 Verfahren zur herstellung von copoly(karbonat/phosphonat)zusammensetzungen DD145756A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/932,840 US4223104A (en)	1978-08-11	1978-08-11	Copoly (carbonate/phosphonate) compositions

Publications (1)

Publication Number	Publication Date
DD145756A5 true DD145756A5 (de)	1981-01-07

Family

ID=25463033

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79214894A DD145756A5 (de)	1978-08-11	1979-08-09	Verfahren zur herstellung von copoly(karbonat/phosphonat)zusammensetzungen

Country Status (11)

Country	Link
US (1)	US4223104A (cs)
EP (1)	EP0008823B1 (cs)
JP (1)	JPS5525476A (cs)
AU (1)	AU525229B2 (cs)
CA (1)	CA1121096A (cs)
CS (1)	CS212326B2 (cs)
DD (1)	DD145756A5 (cs)
DE (1)	DE2963490D1 (cs)
IL (1)	IL57545A (cs)
MA (1)	MA18529A1 (cs)
NO (1)	NO792604L (cs)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2925208A1 (de) *	1979-06-22	1981-01-29	Bayer Ag	Verfahren zur herstellung von aromatischen thermoplastischen polyphosphonatocarbonaten
DE2925207A1 (de) *	1979-06-22	1981-01-29	Bayer Ag	Thermoplastische, verzweigte, aromatische polyphosphonate, ihre verwendung und ein verfahren zu ihrer herstellung
DE3001863A1 (de) *	1980-01-19	1981-07-23	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von thermoplastischen aromatischen polyphosphonatocarbonaten verbesserter thermischer alterungsbestaendigkeit und deren verwendung
US4444978A (en) *	1983-07-29	1984-04-24	The Dow Chemical Company	Thermally stable carbonate polymer
US4474937A (en) *	1983-10-03	1984-10-02	The Dow Chemical Company	Phosphorus-modified polyestercarbonate resins
DE3517271A1 (de) *	1985-05-14	1986-11-20	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von copolyphosphonaten mit hoher kerbschlagzaehigkeit
DE3520296A1 (de) *	1985-06-07	1986-12-11	Bayer Ag, 5090 Leverkusen	Verfahren zur herstellung von copolyphosphonaten mit hoher zaehigkeit
DE3933548A1 (de) *	1989-10-07	1991-04-11	Bayer Ag	Hochverzweigte polyphosphonate
US20040167283A1 (en) *	2003-02-24	2004-08-26	Michael Vinciguerra	Linear polyphosphonates that exhibit an advantageous combination of properties, and methods related thereto
US6861499B2 (en) *	2003-02-24	2005-03-01	Triton Systems, Inc.	Branched polyphosphonates that exhibit an advantageous combination of properties, and methods related thereto
US7645850B2 (en) *	2005-08-11	2010-01-12	Frx Polymers, Inc.	Poly(block-phosphonato-ester) and poly(block-phosphonato-carbonate) and methods of making same
US7666932B2 (en) *	2005-10-17	2010-02-23	Frx Polymers, Inc.	Compositions comprising polyphosphonates and additives that exhibit an advantageous combination of properties, and methods related thereto
WO2007079272A2 (en) *	2005-10-18	2007-07-12	Frx Polymers Llc	Diaryl alkylphosphonates and methods for preparing same
US7838604B2 (en)	2005-12-01	2010-11-23	Frx Polymers, Inc.	Method for the production of block copolycarbonate/phosphonates and compositions therefrom
US7928259B2 (en) *	2008-02-12	2011-04-19	Frx Polymers, Inc.	Diaryl alkylphosphonates and methods for preparing same
US9441877B2 (en)	2010-03-17	2016-09-13	Chart Inc.	Integrated pre-cooled mixed refrigerant system and method
JP5964307B2 (ja)	2010-09-16	2016-08-03	エフアールエックスポリマーズ、インク．	ビスフェノールを基本とした高分子量ランダムコポリ（ホスホネートカーボネート）
KR20140086774A (ko) *	2012-12-28	2014-07-08	제일모직주식회사	분지형 폴리카보네이트 및 이의 제조방법
TW201439222A (zh)	2013-01-22	2014-10-16	Frx Polymers Inc	含磷環氧化合物及源自其之組成物
US11408673B2 (en)	2013-03-15	2022-08-09	Chart Energy & Chemicals, Inc.	Mixed refrigerant system and method
US11428463B2 (en)	2013-03-15	2022-08-30	Chart Energy & Chemicals, Inc.	Mixed refrigerant system and method
WO2014146138A1 (en)	2013-03-15	2014-09-18	Chart Energy & Chemicals, Inc.	Mixed refrigerant system and method
AR105277A1 (es)	2015-07-08	2017-09-20	Chart Energy & Chemicals Inc	Sistema y método de refrigeración mixta

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3094508A (en) *	1959-04-16	1963-06-18	Armstrong Cork Co	Branched polycarbonate and process for preparing same
GB1025422A (en) *	1961-11-30	1966-04-06	Gevaert Photo Prod Nv	Copolyesters and the preparation thereof
BE754758A (fr) *	1969-08-19	1971-01-18	Gen Electric	Composition thermiquement stable a base de polymere de carbonate aromatique et procede pour sa preparation
US3597394A (en) *	1969-10-16	1971-08-03	Mobay Chemical Corp	Branching or crosslinking of polycarbonates
US4001183A (en) *	1971-03-19	1977-01-04	Bayer Aktiengesellschaft	Tetraphenol containing polycarbonates
US3766139A (en) *	1971-07-29	1973-10-16	Gen Electric	Thermal oxidatively stable polycarbonate composition
DE2254918A1 (de) *	1972-11-09	1974-05-16	Bayer Ag	Verzweigte aromatische polycarbonate

1978
- 1978-08-11 US US05/932,840 patent/US4223104A/en not_active Expired - Lifetime
1979
- 1979-06-12 IL IL57545A patent/IL57545A/xx unknown
- 1979-06-15 AU AU48134/79A patent/AU525229B2/en not_active Ceased
- 1979-06-22 CA CA000330353A patent/CA1121096A/en not_active Expired
- 1979-07-06 JP JP8581279A patent/JPS5525476A/ja active Pending
- 1979-07-16 MA MA18726A patent/MA18529A1/fr unknown
- 1979-08-02 CS CS795339A patent/CS212326B2/cs unknown
- 1979-08-08 DE DE7979200438T patent/DE2963490D1/de not_active Expired
- 1979-08-08 EP EP79200438A patent/EP0008823B1/en not_active Expired
- 1979-08-09 DD DD79214894A patent/DD145756A5/de unknown
- 1979-08-10 NO NO792604A patent/NO792604L/no unknown

Also Published As

Publication number	Publication date
IL57545A (en)	1983-07-31
US4223104A (en)	1980-09-16
CS212326B2 (en)	1982-03-26
NO792604L (no)	1980-02-12
JPS5525476A (en)	1980-02-23
DE2963490D1 (en)	1982-09-30
EP0008823B1 (en)	1982-08-04
CA1121096A (en)	1982-03-30
AU4813479A (en)	1980-02-14
MA18529A1 (fr)	1980-04-01
IL57545A0 (en)	1979-10-31
AU525229B2 (en)	1982-10-28
EP0008823A1 (en)	1980-03-19

Publication	Publication Date	Title
DD145756A5 (de)	1981-01-07	Verfahren zur herstellung von copoly(karbonat/phosphonat)zusammensetzungen
DE1720894C3 (de)	1980-09-25	Copolycarbonate
DE1570703A1 (de)	1970-02-12	Hydrolytisch stabile Polycarbonate sowie Verfahren zu deren Herstellung
DE3016019A1 (de)	1980-11-13	Verfahren zur herstellung von polyester/carbonat-mischpolymeren
DE2938464A1 (de)	1981-04-09	Thermoplastische polycarbonate, ihre herstellung und ihre verwendung als formkoerper und folien
DE2211957A1 (de)	1973-09-27	Hochmolekulare, statistische copolycarbonate
DE2721596C2 (de)	1983-02-03	Flammhemmendes Polycarbonat mit verbesserter kritischer Dicke und Verfahren zu seiner Herstellung
DE3344911A1 (de)	1985-06-13	Thermoplastische polysiloxan-polyester(carbonat)-blockcopolymere, ihre herstellung und verwendung
DE69831714T2 (de)	2006-07-06	Verzweigungsmittel für reaktive Extrusion
DE68927370T2 (de)	1997-05-28	Flammenthemmende Polycarbonatmischungen
DE3437785A1 (de)	1985-05-02	Aromatische thermoplastische polymere mit verbesserter formbestaendigkeit
DE69731805T2 (de)	2005-11-24	Orthoesters als Biphenol A-Fänger in Polycarbonatprodukten
DE3143252A1 (de)	1983-05-11	Verfahren zur herstellung von polycarbonaten mit verbessertem alterungsverhalten
DE2254918A1 (de)	1974-05-16	Verzweigte aromatische polycarbonate
DE69532784T2 (de)	2005-03-17	Herstellung von Copolyestercarbonaten nach dem Bischlorkohlensäureester-Prozess
DE69419818T2 (de)	2000-04-27	Bisphosphin-oxid Monomere und damit hergestellte Polycarbonate
DE2040251A1 (de)	1971-02-25	Copolycarbonatzusammensetzung
DE2658849A1 (de)	1977-07-07	Stabilisierte polycarbonatzusammensetzung
DE1770129A1 (de)	1972-02-10	Polycarbonat-Carbamate
DE2321055C2 (de)	1982-06-09	Flammwidrige Polycarbonatformmassen
EP0075772B1 (de)	1986-01-08	Verfahren zur Isolierung von Polycarbonaten auf Basis von 4,4-Dihydroxidiphenylsulfonen
DE2255639C3 (de)	1981-11-19	Ester der phosphorigen Säure
EP0102573B1 (de)	1986-02-26	Polycarbonate mit konjugierte Doppelbindungen enthaltenden Endgruppen, gegebenenfalls im Gemisch mit bekannten aromatischen Polycarbonaten, ihre Herstellung und ihre Verwendung
DE2904832A1 (de)	1980-08-14	Thermoplastische massen, verfahren zu ihrer herstellung sowie ihre verwendung
DE3330129A1 (de)	1984-02-23	Aromatische polycarbonate mit hohem molekulargewicht mit verbesserter verarbeitbarkeit