NO132435B - - Google Patents

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Info

Publication number: NO132435B
Authority: NO; Norway
Prior art keywords: carbon atoms; molding compounds; acid; compounds according; alkaline earth
Prior art date: 1970-09-02

Application number

NO3255/71A

Other languages

English (en)

Norwegian (no)

Other versions

NO132435C (ja

Inventor

E Wolters

G Roos

Original Assignee

Hoechst Ag

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.)

1970-09-02

Filing date

1971-09-01

Publication date

1975-08-04

1971-09-01 Application filed by Hoechst Ag filed Critical Hoechst Ag

1975-08-04 Publication of NO132435B publication Critical patent/NO132435B/no

1975-11-12 Publication of NO132435C publication Critical patent/NO132435C/no

Links

-1 polyoxymethylenes Polymers 0.000 claims description 32
239000003381 stabilizer Substances 0.000 claims description 28
150000001875 compounds Chemical class 0.000 claims description 27
229920006324 polyoxymethylene Polymers 0.000 claims description 21
125000004432 carbon atom Chemical group C* 0.000 claims description 17
238000000465 moulding Methods 0.000 claims description 12
239000002253 acid Substances 0.000 claims description 10
150000002148 esters Chemical class 0.000 claims description 9
229930040373 Paraformaldehyde Natural products 0.000 claims description 7
150000001735 carboxylic acids Chemical class 0.000 claims description 5
150000003839 salts Chemical class 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 3
125000001931 aliphatic group Chemical group 0.000 claims description 3
229910052791 calcium Inorganic materials 0.000 claims description 3
239000011575 calcium Substances 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
159000000007 calcium salts Chemical class 0.000 claims description 2
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 2
229920006395 saturated elastomer Polymers 0.000 claims description 2
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 claims description 2
150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 1
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 13
BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 9
229920001577 copolymer Polymers 0.000 description 8
229920000642 polymer Polymers 0.000 description 7
230000004580 weight loss Effects 0.000 description 7
230000000052 comparative effect Effects 0.000 description 6
125000004122 cyclic group Chemical group 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000008187 granular material Substances 0.000 description 6
230000000087 stabilizing effect Effects 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
238000010438 heat treatment Methods 0.000 description 5
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
239000002904 solvent Substances 0.000 description 4
230000002195 synergetic effect Effects 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
150000004292 cyclic ethers Chemical class 0.000 description 3
238000001035 drying Methods 0.000 description 3
238000005469 granulation Methods 0.000 description 3
230000003179 granulation Effects 0.000 description 3
238000001746 injection moulding Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000002530 phenolic antioxidant Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 2
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
229930185605 Bisphenol Natural products 0.000 description 2
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
239000003963 antioxidant agent Substances 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
238000002845 discoloration Methods 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
229920000620 organic polymer Polymers 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
238000003860 storage Methods 0.000 description 2
230000008646 thermal stress Effects 0.000 description 2
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
AUAGGMPIKOZAJZ-UHFFFAOYSA-N 1,3,6-trioxocane Chemical compound C1COCOCCO1 AUAGGMPIKOZAJZ-UHFFFAOYSA-N 0.000 description 1
CZLMRJZAHXYRIX-UHFFFAOYSA-N 1,3-dioxepane Chemical compound C1CCOCOC1 CZLMRJZAHXYRIX-UHFFFAOYSA-N 0.000 description 1
BQLZNUMAQHULJO-UHFFFAOYSA-N 1,3-dioxonane Chemical compound C1CCCOCOCC1 BQLZNUMAQHULJO-UHFFFAOYSA-N 0.000 description 1
HPILSDOMLLYBQF-UHFFFAOYSA-N 2-[1-(oxiran-2-ylmethoxy)butoxymethyl]oxirane Chemical compound C1OC1COC(CCC)OCC1CO1 HPILSDOMLLYBQF-UHFFFAOYSA-N 0.000 description 1
SBZGDCNVZHJKIS-UHFFFAOYSA-N 2-[4-hydroxy-3,5-di(propan-2-yl)phenyl]acetic acid Chemical compound CC(C)C1=CC(CC(O)=O)=CC(C(C)C)=C1O SBZGDCNVZHJKIS-UHFFFAOYSA-N 0.000 description 1
YEXOWHQZWLCHHD-UHFFFAOYSA-N 3,5-ditert-butyl-4-hydroxybenzoic acid Chemical compound CC(C)(C)C1=CC(C(O)=O)=CC(C(C)(C)C)=C1O YEXOWHQZWLCHHD-UHFFFAOYSA-N 0.000 description 1
IUDNGVFSUHFMCF-UHFFFAOYSA-N 4-(chloromethyl)-1,3-dioxolane Chemical compound ClCC1COCO1 IUDNGVFSUHFMCF-UHFFFAOYSA-N 0.000 description 1
HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
239000005639 Lauric acid Substances 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000032683 aging Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001409 amidines Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
239000012965 benzophenone Substances 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
238000007664 blowing Methods 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
239000008116 calcium stearate Substances 0.000 description 1
235000013539 calcium stearate Nutrition 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical class OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000007334 copolymerization reaction Methods 0.000 description 1
ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical compound C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 description 1
FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohexene oxide Natural products O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
150000002118 epoxides Chemical class 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000011888 foil Substances 0.000 description 1
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
230000008642 heat stress Effects 0.000 description 1
150000002429 hydrazines Chemical class 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
125000004464 hydroxyphenyl group Chemical group 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000002074 melt spinning Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
238000000034 method Methods 0.000 description 1
239000000178 monomer Substances 0.000 description 1
229910052757 nitrogen Inorganic materials 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
AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000003825 pressing Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical class CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Chemical class CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
229960003656 ricinoleic acid Drugs 0.000 description 1
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000011265 semifinished product Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
239000008117 stearic acid Chemical class 0.000 description 1
238000003756 stirring Methods 0.000 description 1
230000035882 stress Effects 0.000 description 1
229910052712 strontium Inorganic materials 0.000 description 1
CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000003464 sulfur compounds Chemical class 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
150000003585 thioureas Chemical class 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
238000004383 yellowing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
- C08K5/134—Phenols containing ester groups
- C08K5/1345—Carboxylic esters of phenolcarboxylic acids

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)

NO3255/71A 1970-09-02 1971-09-01 NO132435C (ja)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2043498A DE2043498C3 (de)	1970-09-02	1970-09-02	Stabilisierte Formmassen aus Polyoxymethylenen

Publications (2)

Publication Number	Publication Date
NO132435B true NO132435B (ja)	1975-08-04
NO132435C NO132435C (ja)	1975-11-12

Family

ID=5781371

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO3255/71A NO132435C (ja)	1970-09-02	1971-09-01

Country Status (16)

Country	Link
US (1)	US3743614A (ja)
JP (1)	JPS5522508B1 (ja)
AT (1)	AT309820B (ja)
BE (1)	BE772017A (ja)
CA (1)	CA964791A (ja)
CH (1)	CH549617A (ja)
DE (1)	DE2043498C3 (ja)
ES (3)	ES394577A1 (ja)
FI (1)	FI56021C (ja)
FR (1)	FR2105196B1 (ja)
GB (1)	GB1321184A (ja)
NL (1)	NL170014C (ja)
NO (1)	NO132435C (ja)
PL (1)	PL77822B1 (ja)
SE (1)	SE427113B (ja)
SU (1)	SU466685A3 (ja)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3903197A (en) *	1970-05-28	1975-09-02	Asahi Chemical Ind	Polyacetal composition
JPS5538988B2 (ja) *	1972-04-19	1980-10-07
JPS6016901B2 (ja) *	1978-10-25	1985-04-30	ポリプラスチツクス株式会社	水汚染の少いポリアセタ−ル樹脂成形品
JPS5618640A (en) *	1979-07-24	1981-02-21	Mitsubishi Gas Chem Co Inc	Stabilized oxymethylene copolymer conposition
US4804716A (en) *	1983-02-07	1989-02-14	E. I. Du Pont De Nemours And Company	Toughened polyoxymethylene compositions
US4766168A (en) *	1986-04-15	1988-08-23	E. I. Du Pont De Nemours And Company	Stabilized polyacetal compositions
US4814397A (en) *	1986-04-15	1989-03-21	E. I. Du Pont De Nemours And Company	Stabilized polyacetal compositions
DE3628560A1 (de) *	1986-08-22	1988-03-03	Basf Ag	Polyoximethylen-formmassen mit verbesserter thermischer stabilitaet, verfahren zu deren herstellung und deren verwendung
US5096951A (en) *	1990-12-13	1992-03-17	Hoechst Celanese Corporation	Color stabilized polyoxymethylene molding compositions
US5364900A (en) *	1993-04-08	1994-11-15	Asahi Kasei Kogyo Kabushiki Kaisha	Stabilized acetal resin compositions
DE69516545T2 (de) *	1995-09-29	2001-01-25	Asahi Chemical Ind	Polyacetalharzzusammensetzung
JP3578540B2 (ja)	1996-02-19	2004-10-20	旭化成ケミカルズ株式会社	エージング性に優れたポリアセタール樹脂組成物
DE19815663B4 (de) *	1998-04-08	2010-09-09	Ticona Gmbh	Verwendung von Polyoxymethylen-Formmassen mit verbesserter Verarbeitungsstabilität und verminderter Emissionsneigung zur Herstellung von Formteilen
US20040063853A1 (en) *	1998-04-08	2004-04-01	Stefan Disch	Polyoxymethylene moulding material with improved processing stability and a reduced emissions tendency
ES2312579T3 (es) *	2001-04-30	2009-03-01	Ciba Holding Inc.	Articulos moldeados de poliacetal estabilizados frente a la decoloracion.
DE10129535A1 (de) *	2001-06-21	2003-01-09	Basf Ag	Dieselkraftstoffbeständige Formteile
WO2014050448A1 (ja) *	2012-09-26	2014-04-03	三菱瓦斯化学株式会社	ポリアセタール延伸繊維
EP2886569B1 (en)	2013-12-20	2016-04-20	Politechnika Poznanska	'polyoxymethylene composite with reduced formaldehyde emission and method for making and use thereof'

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1694144A1 (de) *	1967-04-08	1971-07-29	Hoechst Ag	Verfahren zum Stabilisieren von Polyacetalen
DE1937661B2 (de) *	1969-07-24	1972-11-16	Farbwerke Hoechst AG, vormals Meister Lucius & Brüning, 6000 Frankfurt	Stabilisierte formmassen aus polyacetalen

1970
- 1970-09-02 DE DE2043498A patent/DE2043498C3/de not_active Expired
1971
- 1971-08-19 CA CA120,887A patent/CA964791A/en not_active Expired
- 1971-08-27 ES ES394577A patent/ES394577A1/es not_active Expired
- 1971-08-27 SU SU1694609A patent/SU466685A3/ru active
- 1971-08-27 NL NLAANVRAGE7111831,A patent/NL170014C/xx not_active IP Right Cessation
- 1971-08-30 CH CH1271871A patent/CH549617A/xx not_active IP Right Cessation
- 1971-08-31 FI FI2427/71A patent/FI56021C/fi active
- 1971-08-31 US US00176693A patent/US3743614A/en not_active Expired - Lifetime
- 1971-08-31 BE BE772017A patent/BE772017A/xx unknown
- 1971-08-31 GB GB4057671A patent/GB1321184A/en not_active Expired
- 1971-09-01 PL PL1971150300A patent/PL77822B1/pl unknown
- 1971-09-01 SE SE7111078A patent/SE427113B/xx unknown
- 1971-09-01 NO NO3255/71A patent/NO132435C/no unknown
- 1971-09-01 JP JP6669171A patent/JPS5522508B1/ja active Pending
- 1971-09-01 AT AT762971A patent/AT309820B/de not_active IP Right Cessation
- 1971-09-02 FR FR7131767A patent/FR2105196B1/fr not_active Expired
1973
- 1973-08-27 ES ES418257A patent/ES8704985A2/es not_active Expired
1974
- 1974-01-05 ES ES422060A patent/ES422060A2/es not_active Expired

Also Published As

Publication number	Publication date
GB1321184A (en)	1973-06-20
ES8704985A2 (es)	1986-06-16
BE772017A (fr)	1972-02-29
ES394577A1 (es)	1982-05-01
FR2105196B1 (ja)	1976-02-13
SU466685A3 (ru)	1975-04-05
DE2043498A1 (de)	1972-03-09
CA964791A (en)	1975-03-18
DE2043498C3 (de)	1984-09-06
ES422060A2 (es)	1984-11-16
US3743614A (en)	1973-07-03
NL7111831A (ja)	1972-03-06
NL170014B (nl)	1982-04-16
DE2043498B2 (de)	1973-08-02
PL77822B1 (en)	1975-04-30
JPS5522508B1 (ja)	1980-06-17
NL170014C (nl)	1982-09-16
NO132435C (ja)	1975-11-12
AT309820B (de)	1973-09-10
SE427113B (sv)	1983-03-07
FI56021B (fi)	1979-07-31
CH549617A (de)	1974-05-31
FI56021C (fi)	1979-11-12
FR2105196A1 (ja)	1972-04-28

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NO132435B (ja)	1975-08-04
WO2007020931A1 (ja)	2007-02-22	ポリアセタール樹脂組成物及び樹脂成形体
NO116876B (ja)	1969-06-02
KR102499911B1 (ko)	2023-02-14	폴리아세탈 수지 조성물, 압출 성형품 및 사출 성형품
BR112016011298B1 (pt)	2022-05-17	Método para produção de composição de resina de polioximetileno
JP2006510755A (ja)	2006-03-30	メラミンベースの難燃剤の製造方法及びポリマー組成物
NO140721B (no)	1979-07-16	Stabiliserte formmasser av polyoksymetylener
DE4436107A1 (de)	1996-04-11	Polyacetalformmasse, Verfahren zu ihrer Herstellung und ihre Verwendung
US3969292A (en)	1976-07-13	Stabilized molding compositions based on poly(oxymethylene)
US11390740B2 (en)	2022-07-19	Polyacetal resin composition and method for producing the same
NO141721B (no)	1980-01-21	Stabiliserte formmasser av polyoksymetylener
US11820857B2 (en)	2023-11-21	Method for producing oxymethylene copolymer resin composition, and oxymethylene copolymer resin composition
EP2123710A1 (en)	2009-11-25	Polyacetal resin composition
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JPH02166151A (ja)	1990-06-26	ポリオキシメチレン組成物
US3280068A (en)	1966-10-18	Polyoxymethylenes containing allophanates as stabilizers
DE1937661A1 (de)	1971-02-18	Stabilisierte Formmassen aus Polyacetalen
DE2365644C3 (de)	1977-11-03	Stabilisatorkombination für Polyoxymethylene
DE10248630B4 (de)	2006-09-07	Diaminotriazinylverbindungen, Verfahren zu deren Herstellung, Zusammensetzung enthaltend diese und deren Verwendung
DE2350415C3 (de)	1976-08-05	Formmasse auf Poly (oxy methylen)-Basis
JPS6081242A (ja)	1985-05-09	アセタ−ル樹脂組成物
DE2350415B2 (de)	1976-01-02	Formmasse auf Poly(oxymethylen)-Basis
DE2301351B2 (de)	1975-11-20	Stabilisierte Formmassen aus PoIyoxymethylenen