IL28152A - Modified polyester composition - Google Patents

Modified polyester composition

Info

Publication number: IL28152A
Authority: IL; Israel
Prior art keywords: ester; composition; molecular weight; weight; polyalkylene oxide
Prior art date: 1966-06-20

Application number

IL28152A

Other languages

English (en)

Original Assignee

Monsanto 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.)

1966-06-20

Filing date

1967-06-18

Publication date

1970-09-17

1967-06-18 Application filed by Monsanto Co filed Critical Monsanto Co

1970-09-17 Publication of IL28152A publication Critical patent/IL28152A/en

Links

229920000728 polyester Polymers 0.000 title claims description 45
239000000203 mixture Substances 0.000 title claims description 22
229920000233 poly(alkylene oxides) Polymers 0.000 claims description 22
-1 polyethylene terephthalate Polymers 0.000 claims description 19
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 18
239000002202 Polyethylene glycol Substances 0.000 claims description 14
229920001223 polyethylene glycol Polymers 0.000 claims description 14
229920000139 polyethylene terephthalate Polymers 0.000 claims description 14
239000005020 polyethylene terephthalate Substances 0.000 claims description 14
239000003795 chemical substances by application Substances 0.000 claims description 12
150000002148 esters Chemical class 0.000 claims description 12
238000003756 stirring Methods 0.000 claims description 11
238000002360 preparation method Methods 0.000 claims description 5
238000000034 method Methods 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 3
239000004698 Polyethylene Substances 0.000 claims description 2
150000005840 aryl radicals Chemical group 0.000 claims description 2
229920000573 polyethylene Polymers 0.000 claims description 2
239000004744 fabric Substances 0.000 description 22
230000003068 static effect Effects 0.000 description 20
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 19
239000000835 fiber Substances 0.000 description 12
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 10
229920002959 polymer blend Polymers 0.000 description 9
229910001220 stainless steel Inorganic materials 0.000 description 9
239000010935 stainless steel Substances 0.000 description 9
239000000975 dye Substances 0.000 description 7
239000000463 material Substances 0.000 description 7
229920000642 polymer Polymers 0.000 description 7
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
239000005711 Benzoic acid Substances 0.000 description 5
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
235000010233 benzoic acid Nutrition 0.000 description 5
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 5
238000004519 manufacturing process Methods 0.000 description 5
229920001634 Copolyester Polymers 0.000 description 4
239000006085 branching agent Substances 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
150000001991 dicarboxylic acids Chemical class 0.000 description 4
150000002334 glycols Chemical class 0.000 description 4
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
238000012360 testing method Methods 0.000 description 4
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
239000003431 cross linking reagent Substances 0.000 description 3
238000004900 laundering Methods 0.000 description 3
238000005259 measurement Methods 0.000 description 3
238000012545 processing Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
239000000428 dust Substances 0.000 description 2
230000005611 electricity Effects 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000002074 melt spinning Methods 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
238000010998 test method Methods 0.000 description 2
238000001291 vacuum drying Methods 0.000 description 2
DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
229940035437 1,3-propanediol Drugs 0.000 description 1
229940043375 1,5-pentanediol Drugs 0.000 description 1
ALVZNPYWJMLXKV-UHFFFAOYSA-N 1,9-Nonanediol Chemical compound OCCCCCCCCCO ALVZNPYWJMLXKV-UHFFFAOYSA-N 0.000 description 1
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
QACUUGBVDGMIQH-UHFFFAOYSA-N 4-(1-carboxybutoxy)benzoic acid Chemical compound CCCC(C(O)=O)OC1=CC=C(C(O)=O)C=C1 QACUUGBVDGMIQH-UHFFFAOYSA-N 0.000 description 1
ZOPFZPGPAKRUFE-UHFFFAOYSA-N 4-(1-carboxyethoxy)benzoic acid Chemical compound OC(=O)C(C)OC1=CC=C(C(O)=O)C=C1 ZOPFZPGPAKRUFE-UHFFFAOYSA-N 0.000 description 1
CQIJNTKWTVHOFV-UHFFFAOYSA-N 4-(1-carboxyhexoxy)benzoic acid Chemical compound CCCCCC(C(O)=O)OC1=CC=C(C(O)=O)C=C1 CQIJNTKWTVHOFV-UHFFFAOYSA-N 0.000 description 1
MURBPOMIQLULQU-UHFFFAOYSA-N 4-(1-carboxypentoxy)benzoic acid Chemical compound CCCCC(C(O)=O)OC1=CC=C(C(O)=O)C=C1 MURBPOMIQLULQU-UHFFFAOYSA-N 0.000 description 1
IKRCKEUYLJBWHG-UHFFFAOYSA-N 4-(1-carboxypropoxy)benzoic acid Chemical compound CCC(C(O)=O)OC1=CC=C(C(O)=O)C=C1 IKRCKEUYLJBWHG-UHFFFAOYSA-N 0.000 description 1
LABJFIBQJFPXHZ-UHFFFAOYSA-N 4-(carboxymethoxy)benzoic acid Chemical compound OC(=O)COC1=CC=C(C(O)=O)C=C1 LABJFIBQJFPXHZ-UHFFFAOYSA-N 0.000 description 1
DMEDOWYXHVUPMO-UHFFFAOYSA-N 4-(carboxymethyl)benzoic acid Chemical compound OC(=O)CC1=CC=C(C(O)=O)C=C1 DMEDOWYXHVUPMO-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
241000790917 Dioxys <bee> Species 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
150000007860 aryl ester derivatives Chemical class 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
230000003750 conditioning effect Effects 0.000 description 1
239000004020 conductor Substances 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
238000004043 dyeing Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
229940093476 ethylene glycol Drugs 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
SXCBDZAEHILGLM-UHFFFAOYSA-N heptane-1,7-diol Chemical compound OCCCCCCCO SXCBDZAEHILGLM-UHFFFAOYSA-N 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
239000011872 intimate mixture Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920006324 polyoxymethylene Polymers 0.000 description 1
229920000166 polytrimethylene carbonate Polymers 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000003340 retarding agent Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
238000010408 sweeping Methods 0.000 description 1
235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
239000004753 textile Substances 0.000 description 1
150000005691 triesters Chemical class 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from 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)
Artificial Filaments (AREA)
Polyesters Or Polycarbonates (AREA)
Compositions Of Macromolecular Compounds (AREA)

IL28152A 1966-06-20 1967-06-18 Modified polyester composition IL28152A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US558633A US3410927A (en)	1966-06-20	1966-06-20	Polyester filaments containing polyethylene glycol esters

Publications (1)

Publication Number	Publication Date
IL28152A true IL28152A (en)	1970-09-17

Family

ID=24230309

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL28152A IL28152A (en)	1966-06-20	1967-06-18	Modified polyester composition

Country Status (8)

Country	Link
US (1)	US3410927A (fr)
BE (1)	BE700214A (fr)
CH (1)	CH487207A (fr)
DE (1)	DE1694625A1 (fr)
GB (1)	GB1196803A (fr)
IL (1)	IL28152A (fr)
LU (1)	LU53904A1 (fr)
NL (1)	NL6708584A (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4035441A (en) *	1973-06-26	1977-07-12	Toray Industries, Inc.	Polyester filament having excellent antistatic properties and process for preparing the same
US4795771A (en) *	1986-02-26	1989-01-03	Toyo Boseki Kabushiki Kaisha	Polyester composition
WO1994003544A1 (fr)	1992-07-29	1994-02-17	Baxter International Inc.	Biomateriaux a surface hydrophile
DE102008032205A1 (de)	2008-07-09	2010-01-14	Lanxess Deutschland Gmbh	Fließverbesserte Thermoplasten

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2393863A (en) *	1942-03-26	1946-01-29	Bakelite Corp	Antistatic composition
US3329557A (en) *	1955-04-06	1967-07-04	Du Pont	Static resistant filament and process therefor
US2993234A (en) *	1958-02-28	1961-07-25	Tokyo Shibaura Electric Co	Method of manufacturing antistatic record disks
BE623762A (fr) *	1961-10-20	1963-04-18
US3177174A (en) *	1961-12-07	1965-04-06	Grace W R & Co	Non-static polyolefin-polyethylene glycol stearate ester composition
US3355413A (en) *	1966-10-14	1967-11-28	Eastman Kodak Co	Polyester fibers resistant to resoiling during laundering

1966
- 1966-06-20 US US558633A patent/US3410927A/en not_active Expired - Lifetime
1967
- 1967-06-16 LU LU53904D patent/LU53904A1/xx unknown
- 1967-06-18 IL IL28152A patent/IL28152A/en unknown
- 1967-06-20 CH CH871767A patent/CH487207A/fr not_active IP Right Cessation
- 1967-06-20 BE BE700214D patent/BE700214A/xx unknown
- 1967-06-20 DE DE19671694625 patent/DE1694625A1/de active Pending
- 1967-06-20 GB GB27832/67A patent/GB1196803A/en not_active Expired
- 1967-06-20 NL NL6708584A patent/NL6708584A/xx unknown

Also Published As

Publication number	Publication date
CH487207A (fr)	1970-03-15
GB1196803A (en)	1970-07-01
NL6708584A (fr)	1967-12-21
DE1694625A1 (de)	1971-08-12
LU53904A1 (fr)	1968-03-08
BE700214A (fr)	1967-12-20
US3410927A (en)	1968-11-12

Publication	Publication Date	Title
US3839245A (en)	1974-10-01	Poly(ether-ester-amide) antistatic compositions derived from dimr acids
US3557039A (en)	1971-01-19	Aqueous dispersion of block or graft polymer useful in surface modifying treatment of polyester shaped articles
US3652713A (en)	1972-03-28	Polyester composition having improved antistatic properties and process for the preparation thereof
US3616183A (en)	1971-10-26	Polyester sheath-core conjugate filaments
US4165303A (en)	1979-08-21	Polymer compositions containing poly (alkylene ether) esters of polybasic acids
US3388104A (en)	1968-06-11	Polycarbonamides having an improved antistatic property
US3410927A (en)	1968-11-12	Polyester filaments containing polyethylene glycol esters
US3487453A (en)	1969-12-30	Dyeable polypropylene containing a polyetherester
US3970635A (en)	1976-07-20	Fire retardant polyester fibers
JPH03182546A (ja)	1991-08-08	ポリエステル組成物および繊維
US3620823A (en)	1971-11-16	Process of improving the resistance of soiling of melt spun fibers
US3492368A (en)	1970-01-27	Fiber forming linear polyesters with improved dyeability
US3654235A (en)	1972-04-04	Antistatic polycarbonamide filaments
US3620824A (en)	1971-11-16	White thermally stable polyether modified polyester fibers and method of production
US3637552A (en)	1972-01-25	Flame retardant antistatic polymers
JPS6011944B2 (ja)	1985-03-29	制電性ポリエステル組成物
CA1111187A (fr)	1981-10-20	Copolyesters auto-extincteurs et thermostables, et methode de fabrication connexe
US3962185A (en)	1976-06-08	Polyester compositions having a durable antistatic property
US3607804A (en)	1971-09-21	Dyeable pill resistant polyesters
US3700642A (en)	1972-10-24	Polyester-polyoxyalkylene sulfonate compositions
JPS62149914A (ja)	1987-07-03	改質ポリエステル繊維
US3560449A (en)	1971-02-02	Internal antistatic agent for polyamide use and polyamide compositions having improved antistatic property
JPS62149913A (ja)	1987-07-03	改質ポリエステル繊維
US3879170A (en)	1975-04-22	Method of acid dyeing polyester fibers
JPH04153319A (ja)	1992-05-26	制電性ポリエスエル繊維