PL90957B3 - Stabilized osymethylene polymers[gb1419040a] - Google Patents
Stabilized osymethylene polymers[gb1419040a] Download PDFInfo
- Publication number
- PL90957B3 PL90957B3 PL1974168052A PL16805274A PL90957B3 PL 90957 B3 PL90957 B3 PL 90957B3 PL 1974168052 A PL1974168052 A PL 1974168052A PL 16805274 A PL16805274 A PL 16805274A PL 90957 B3 PL90957 B3 PL 90957B3
- Authority
- PL
- Poland
- Prior art keywords
- streaks
- carbon atoms
- stabilized
- formula
- alkaline earth
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 10
- 150000001875 compounds Chemical class 0.000 claims abstract 7
- 239000000203 mixture Substances 0.000 claims abstract 5
- 229910052791 calcium Inorganic materials 0.000 claims abstract 3
- 239000011575 calcium Substances 0.000 claims abstract 3
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 claims abstract 3
- 229960002401 calcium lactate Drugs 0.000 claims abstract 3
- 239000001527 calcium lactate Substances 0.000 claims abstract 3
- 235000011086 calcium lactate Nutrition 0.000 claims abstract 3
- 229920001577 copolymer Polymers 0.000 claims abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 3
- 239000001257 hydrogen Substances 0.000 claims abstract 3
- 150000003839 salts Chemical class 0.000 claims abstract 3
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 2
- 229910052749 magnesium Inorganic materials 0.000 claims abstract 2
- 239000011777 magnesium Substances 0.000 claims abstract 2
- 159000000003 magnesium salts Chemical class 0.000 claims abstract 2
- -1 polyoxymethylene Polymers 0.000 claims 17
- 229920006324 polyoxymethylene Polymers 0.000 claims 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 5
- 229930040373 Paraformaldehyde Natural products 0.000 claims 4
- 150000001735 carboxylic acids Chemical class 0.000 claims 4
- 239000002253 acid Substances 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 2
- 229960005069 calcium Drugs 0.000 claims 2
- 150000004292 cyclic ethers Chemical class 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 claims 2
- 235000011437 Amygdalus communis Nutrition 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- 241000220304 Prunus dulcis Species 0.000 claims 1
- 235000021355 Stearic acid Nutrition 0.000 claims 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 235000020224 almond Nutrition 0.000 claims 1
- 150000005840 aryl radicals Chemical class 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 208000020442 loss of weight Diseases 0.000 claims 1
- OVGXLJDWSLQDRT-UHFFFAOYSA-L magnesium lactate Chemical compound [Mg+2].CC(O)C([O-])=O.CC(O)C([O-])=O OVGXLJDWSLQDRT-UHFFFAOYSA-L 0.000 claims 1
- 229960004658 magnesium lactate Drugs 0.000 claims 1
- 239000000626 magnesium lactate Substances 0.000 claims 1
- 235000015229 magnesium lactate Nutrition 0.000 claims 1
- 229940091250 magnesium supplement Drugs 0.000 claims 1
- 238000000465 moulding Methods 0.000 claims 1
- CRSOQBOWXPBRES-UHFFFAOYSA-N neopentane Chemical compound CC(C)(C)C CRSOQBOWXPBRES-UHFFFAOYSA-N 0.000 claims 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 1
- WBHHMMIMDMUBKC-QJWNTBNXSA-M ricinoleate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O WBHHMMIMDMUBKC-QJWNTBNXSA-M 0.000 claims 1
- 229940066675 ricinoleate Drugs 0.000 claims 1
- WBHHMMIMDMUBKC-QJWNTBNXSA-N ricinoleic acid Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O WBHHMMIMDMUBKC-QJWNTBNXSA-N 0.000 claims 1
- 229960003656 ricinoleic acid Drugs 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 239000008117 stearic acid Substances 0.000 claims 1
- 150000003628 tricarboxylic acids Chemical class 0.000 claims 1
- 238000004383 yellowing Methods 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract 2
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 abstract 2
- ZVVFVKJZNVSANF-UHFFFAOYSA-N 6-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]hexyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCCCCCCOC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 ZVVFVKJZNVSANF-UHFFFAOYSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 229910052788 barium Inorganic materials 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 235000013877 carbamide Nutrition 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- WZHCOOQXZCIUNC-UHFFFAOYSA-N cyclandelate Chemical class C1C(C)(C)CC(C)CC1OC(=O)C(O)C1=CC=CC=C1 WZHCOOQXZCIUNC-UHFFFAOYSA-N 0.000 abstract 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 229920001519 homopolymer Polymers 0.000 abstract 1
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical group 0.000 abstract 1
- 238000001746 injection moulding Methods 0.000 abstract 1
- 239000004611 light stabiliser Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 230000002787 reinforcement Effects 0.000 abstract 1
- 230000006641 stabilisation Effects 0.000 abstract 1
- 238000011105 stabilization Methods 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 229910052712 strontium Inorganic materials 0.000 abstract 1
- 150000003627 tricarboxylic acid derivatives Chemical class 0.000 abstract 1
- 150000003672 ureas Chemical class 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 abstract 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
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic 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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Claims (7)
- Zastrzezenia patentowe 1. Stabilizowane tloczywa z polioksymetylenów o zawartosci 0,05—4% wagowych, w odniesieniu do polioksymetylenu. zwiazków o wzorze 1, w którym F^oznacza rodnik alkilowy o 1—6 atomach wegla, R2 oznacza atom wodoru albo rodnik alkilowy ó1—6 atomach wegla, A oznacza dwu- do szesciowartosciowy, alifatyczny rodnik weglowodorowy o 1—12 atomach wegla i m oznacza zero albo liczbe calkowita 1—6 i n odpowiada wartosciowosci A, oraz 0,01—3% wagowych w odniesieniu do polioksymetylenu, soli metali ziem alkalicznych kwasów karboksylowych. wedlug patentu glównego nr 77822, znamienne tym, ze, zawieraja jako sole metali ziem alkalicznych kwasów karboksylowych sole metali ziem alkalicznych kwasów jedno-, dwu- albo trójkarboksylowych o 2—9 atomach wegla albo aryloalifatycznych lub aromatycznych kwasów karboksylo¬ wych o 7—9 atomach wegla i ewentualnie 0,01—1% wagowego, w odniesieniu do polioksymetylenu, zwiazków o wzorze 2, w którym R oznacza atom wodoru, grupe cyjanowa, rodnik alkilowy o 1 —12 atomach wegla, rodnik cykloalkilowy o 6—12 atomach wegla albo rodnik arylowy o 6—12 atomach wegla, przy czym wymieniony wyzej rodnik alkilowy, cykloalkilowy lub arylowy kazdorazowo moze byc podstawiony przez 1; 2 albo 3 grupy hydroksylowe.
- 2. Stabilizowane tloczywa wedlug zastrz. 1,znamienne tym, ze jako pol ioksymetyleny zawieraja kopolimery z triokasanu i cyklicznych eterów i/albo cyklicznych acetali i/albo liniowych poliacetali.
- 3. Stabilizowane tloczywa wedlug zastrz. 1,znamienne tym, ze jako po I ioksymetyleny zawieraja kopolimery z trioksanu i trójczlonowego eteru cyklicznego.
- 4. Stabilizowane tloczywa wedlug zastrz. 1,znamienne tym, ze jako zwiazki o wzorze 1 zawieraja estry heksanodiolu-(1,6), trójmetyloetanu albo pentaerytrytu z kwasem /3-(3,5-dwu-l II-rzed.-butylo-4-hydroksyfe- nylo)-propionowym.
- 5. Stabilizowane tloczywa wedlug zastrz. 1,znamienne tym, ze jako sole metali ziem alkalicznych kwasów karboksylowych zawieraja sole wapniowe lub sole magnezowe nasyconych lub nienasyconych, alifatycz¬ nych kwasów karboksylowych o 2—9 atomach wegla
- 6. Stabilizowane tloczywa wedlug zastrz 1,znamienne tym, ze jako sole metali ziem alkalicznych kwasów karboksylowych zawieraja mleczan wapnia albo mleczan magnezu.
- 7. Stabilizowane tloczywa wedlug zastrz. 1,znamienne tym, ze jako zwiazki o wzorze 2 zawieraja cyjaroguanidyne.90957 5 Tablica I Utrata ciezarupo Jakosc Przyklad Sól magnezowa kwasu 45 min 120 min Wartosc zólkniecia powierzchni (%) (%) przed Po ksztaltek A B C I II III IV V VI VII VIII IX X XI XII kwas stearynowy kwas rycynylowy kwas arachidynowy octowego propionowego kapronowego pelargonowego mlekowego jablkowego hydro ksypiwal inowego malonowego adypinowego salicylowego cynamonowego migdalowego 0,82 0,66 0.72 0.80 0,61 0.92 0,84 0,75 1,05 1,22 1.17 0,97 1.01 1.05 0.91 3.3 2.5 2,9 3,1 2.8 3,5 3,1 2,9 3,7 4,1 4,3 3,5 3,9 4,0 3,4 0.8 1.6 3,5 0,4 1,8 0,4 0,1 0,7 1.2 1,4 0.1 0,1 0,4 1.8 0.0 12,2 14,0 23,0 18,9 17,4 13,8 12,2 14,9 18,3 25,0 10.0 11,4 25,0 17,1 15,2 silne smugi silne smugi silne smugi nie ma smug nie ma smug nie ma smug nie ma smug nie ma smug nie ma smug me ma smug nie ma smug nie ma smug nie ma smug nie ma smug nie ma smug Tablica II Sól metalu Strataciezaru Wartosczólkniecia Przyklad 'ziemalkalicznych % przed po D rycynooleinianwapnia 2,8 1,1 17,1 XIII mleczanwapnia 2,6 0,8 15,890 957 R< HoV^(CH2)m-CO-0- A R, WZÓR 1 -1 n NC-NH-C -NH -R II NH WZÓR 2 CH2-(CHR)x-[0-(CH2)z] -O WZÓR 390 957 X f \ FIG.1 : i jr [ f L~ / / . .:'•'- ^/. - , ¦-¦-" . ¦•¦'* ' V. •V. k i 1 J ' J 1 _, FIG.290 957 FIG. 3 s •/ /.K ,tftvT.r-.*\Xrj. !-W V FIG.A \yO i ¦¦-¦:/ Prac. Poligraf. UP PRL naklad 120 + 18 Cena 10 zl PL
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19732301351 DE2301351C3 (de) | 1973-01-12 | Stabilisierte Formmassen aus PoIyoxymethylenen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL90957B3 true PL90957B3 (en) | 1977-02-28 |
Family
ID=5868810
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL1974168052A PL90957B3 (en) | 1973-01-12 | 1974-01-11 | Stabilized osymethylene polymers[gb1419040a] |
Country Status (16)
| Country | Link |
|---|---|
| JP (2) | JPS49104940A (pl) |
| AT (1) | AT332647B (pl) |
| AU (1) | AU474449B2 (pl) |
| BE (1) | BE809707R (pl) |
| BR (1) | BR7400190D0 (pl) |
| CA (1) | CA1004796A (pl) |
| CH (1) | CH569757A5 (pl) |
| DD (1) | DD108761A6 (pl) |
| DK (1) | DK135953C (pl) |
| FI (1) | FI62321C (pl) |
| GB (1) | GB1419040A (pl) |
| IT (1) | IT1046713B (pl) |
| NO (1) | NO141721C (pl) |
| PL (1) | PL90957B3 (pl) |
| SE (1) | SE413776B (pl) |
| SU (1) | SU581879A3 (pl) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5618640A (en) * | 1979-07-24 | 1981-02-21 | Mitsubishi Gas Chem Co Inc | Stabilized oxymethylene copolymer conposition |
| JPH0742409B2 (ja) * | 1987-11-27 | 1995-05-10 | 株式会社東芝 | 金型清掃体及び金型清掃方法 |
| US6156834A (en) * | 1998-03-20 | 2000-12-05 | Asahi Kasei Kogyo Kabushiki Kaisha | Polyacetal resin composition |
| US8779045B2 (en) | 2009-10-15 | 2014-07-15 | Milliken & Company | Thermoplastic polymer composition |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1694144A1 (de) * | 1967-04-08 | 1971-07-29 | Hoechst Ag | Verfahren zum Stabilisieren von Polyacetalen |
-
1974
- 1974-01-07 CA CA189,610A patent/CA1004796A/en not_active Expired
- 1974-01-08 AU AU64281/74A patent/AU474449B2/en not_active Expired
- 1974-01-08 GB GB80174A patent/GB1419040A/en not_active Expired
- 1974-01-09 DD DD175915A patent/DD108761A6/xx unknown
- 1974-01-09 DK DK10174A patent/DK135953C/da not_active IP Right Cessation
- 1974-01-09 CH CH24074A patent/CH569757A5/xx not_active IP Right Cessation
- 1974-01-10 FI FI62/74A patent/FI62321C/fi active
- 1974-01-10 IT IT19292/74A patent/IT1046713B/it active
- 1974-01-11 NO NO740084A patent/NO141721C/no unknown
- 1974-01-11 BR BR74190A patent/BR7400190D0/pt unknown
- 1974-01-11 SE SE7400352A patent/SE413776B/xx not_active IP Right Cessation
- 1974-01-11 AT AT22474*#A patent/AT332647B/de not_active IP Right Cessation
- 1974-01-11 SU SU7401991231A patent/SU581879A3/ru active
- 1974-01-11 PL PL1974168052A patent/PL90957B3/pl unknown
- 1974-01-11 JP JP49006119A patent/JPS49104940A/ja active Pending
- 1974-01-14 BE BE139775A patent/BE809707R/xx active
-
1984
- 1984-08-29 JP JP59178550A patent/JPS6084348A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CH569757A5 (pl) | 1975-11-28 |
| FI62321C (fi) | 1982-12-10 |
| BR7400190D0 (pt) | 1974-08-15 |
| SE413776B (sv) | 1980-06-23 |
| DK135953C (da) | 1978-01-16 |
| FI62321B (fi) | 1982-08-31 |
| GB1419040A (en) | 1975-12-24 |
| DD108761A6 (pl) | 1974-10-12 |
| CA1004796A (en) | 1977-02-01 |
| BE809707R (fr) | 1974-07-15 |
| AU6428174A (en) | 1975-07-10 |
| DK135953B (da) | 1977-07-18 |
| SU581879A3 (ru) | 1977-11-25 |
| NO141721C (no) | 1980-04-30 |
| ATA22474A (de) | 1976-01-15 |
| AT332647B (de) | 1976-10-11 |
| JPS6084348A (ja) | 1985-05-13 |
| NO740084L (no) | 1974-07-15 |
| NO141721B (no) | 1980-01-21 |
| AU474449B2 (en) | 1976-07-22 |
| IT1046713B (it) | 1980-07-31 |
| JPS49104940A (pl) | 1974-10-04 |
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