CH443677A - Verfahren zur Herstellung von Gebilden von verbessertem Aussehen aus Polyoxymethylen oder aus dessen Mischpolymerisaten - Google Patents
Verfahren zur Herstellung von Gebilden von verbessertem Aussehen aus Polyoxymethylen oder aus dessen MischpolymerisatenInfo
- Publication number
- CH443677A CH443677A CH729264A CH729264A CH443677A CH 443677 A CH443677 A CH 443677A CH 729264 A CH729264 A CH 729264A CH 729264 A CH729264 A CH 729264A CH 443677 A CH443677 A CH 443677A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- polyoxymethylene
- copolymers
- radical
- structures
- Prior art date
Links
- -1 polyoxymethylene Polymers 0.000 title claims description 13
- 238000000034 method Methods 0.000 title claims description 11
- 229920006324 polyoxymethylene Polymers 0.000 title claims description 11
- 229930040373 Paraformaldehyde Natural products 0.000 title claims description 10
- 229920001577 copolymer Polymers 0.000 title claims description 10
- 230000003287 optical effect Effects 0.000 claims description 15
- MPIFMUARWKUNQZ-UHFFFAOYSA-N 4-[2-(2-phenylethenyl)phenyl]-2h-benzo[e]benzotriazole Chemical class C=1C=CC=C(C=2C=3N=NNC=3C3=CC=CC=C3C=2)C=1C=CC1=CC=CC=C1 MPIFMUARWKUNQZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000332 coumarinyl group Chemical class O1C(=O)C(=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 150000003216 pyrazines Chemical class 0.000 claims description 3
- 238000007493 shaping process Methods 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 125000001302 tertiary amino group Chemical group 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000003226 pyrazolyl group Chemical group 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 229920004943 Delrin® Polymers 0.000 description 2
- 229920005176 Hostaform® Polymers 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 150000001733 carboxylic acid esters Chemical class 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 235000001671 coumarin Nutrition 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 229910052736 halogen Chemical group 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- YKPQUSLRUFLVDA-UHFFFAOYSA-N $l^{2}-azanylmethane Chemical compound [NH]C YKPQUSLRUFLVDA-UHFFFAOYSA-N 0.000 description 1
- 125000003363 1,3,5-triazinyl group Chemical group N1=C(N=CN=C1)* 0.000 description 1
- FBNAYEYTRHHEOB-UHFFFAOYSA-N 2,3,5-triphenyl-1,3-dihydropyrazole Chemical class N1N(C=2C=CC=CC=2)C(C=2C=CC=CC=2)C=C1C1=CC=CC=C1 FBNAYEYTRHHEOB-UHFFFAOYSA-N 0.000 description 1
- ABEOQSWLOAHSPF-UHFFFAOYSA-N 2-[2-(1,3-benzoxazol-2-yl)ethenyl]-1,3-benzoxazole Chemical class C1=CC=C2OC(C=CC=3OC4=CC=CC=C4N=3)=NC2=C1 ABEOQSWLOAHSPF-UHFFFAOYSA-N 0.000 description 1
- PHBSPYGHSRVOHY-UHFFFAOYSA-N 2-[2-(1,3-benzoxazol-2-yl)thiophen-3-yl]-1,3-benzoxazole Chemical class C1=CC=C2OC(C3=C(C=4OC5=CC=CC=C5N=4)C=CS3)=NC2=C1 PHBSPYGHSRVOHY-UHFFFAOYSA-N 0.000 description 1
- OLUOIVJKRJJSKM-UHFFFAOYSA-N 2-[2-(1h-benzimidazol-2-yl)ethenyl]-1h-benzimidazole Chemical class C1=CC=C2NC(C=CC=3NC4=CC=CC=C4N=3)=NC2=C1 OLUOIVJKRJJSKM-UHFFFAOYSA-N 0.000 description 1
- ZTGKHKPZSMMHNM-UHFFFAOYSA-N 3-(2-phenylethenyl)benzene-1,2-disulfonic acid Chemical class OS(=O)(=O)C1=CC=CC(C=CC=2C=CC=CC=2)=C1S(O)(=O)=O ZTGKHKPZSMMHNM-UHFFFAOYSA-N 0.000 description 1
- AZJHEDNAAWPYJI-UHFFFAOYSA-N 4,5-bis(2-phenylethenyl)oxadiazole Chemical class N1=NOC(C=CC=2C=CC=CC=2)=C1C=CC1=CC=CC=C1 AZJHEDNAAWPYJI-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XTRXBOSGRMJASM-UHFFFAOYSA-N N1=NN=C(C=C1)NC(=C(C1=C(C(=CC=C1)S(=O)(=O)O)S(=O)(=O)O)NC1=NN=NC=C1)C1=CC=CC=C1 Chemical class N1=NN=C(C=C1)NC(=C(C1=C(C(=CC=C1)S(=O)(=O)O)S(=O)(=O)O)NC1=NN=NC=C1)C1=CC=CC=C1 XTRXBOSGRMJASM-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 125000006525 methoxy ethyl amino group Chemical group [H]N(*)C([H])([H])C([H])([H])OC([H])([H])[H] 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000001425 triazolyl group Chemical group 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0041—Optical brightening agents, organic pigments
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)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH729264A CH443677A (de) | 1964-06-04 | 1964-06-04 | Verfahren zur Herstellung von Gebilden von verbessertem Aussehen aus Polyoxymethylen oder aus dessen Mischpolymerisaten |
| BE652264D BE652264A (en]) | 1964-06-04 | 1964-08-25 | |
| FR19403A FR1436994A (fr) | 1964-06-04 | 1965-06-03 | Perfectionnements apportés aux matières polymères, en particulier aux articles en polyoxyméthylène ou en copolymères de polyoxyméthylène |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH729264A CH443677A (de) | 1964-06-04 | 1964-06-04 | Verfahren zur Herstellung von Gebilden von verbessertem Aussehen aus Polyoxymethylen oder aus dessen Mischpolymerisaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH443677A true CH443677A (de) | 1967-09-15 |
Family
ID=4322836
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH729264A CH443677A (de) | 1964-06-04 | 1964-06-04 | Verfahren zur Herstellung von Gebilden von verbessertem Aussehen aus Polyoxymethylen oder aus dessen Mischpolymerisaten |
Country Status (2)
| Country | Link |
|---|---|
| BE (1) | BE652264A (en]) |
| CH (1) | CH443677A (en]) |
-
1964
- 1964-06-04 CH CH729264A patent/CH443677A/de unknown
- 1964-08-25 BE BE652264D patent/BE652264A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BE652264A (en]) | 1964-12-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2907729A1 (de) | Zusammensetzung auf der basis von polyaethylenterephthalat | |
| DE2740092B2 (de) | Polyamidharzmasse | |
| CH644617A5 (de) | Zusammensetzung auf der basis von polyaethylenterephthalat -homo oder -copolymerisat. | |
| DE701837C (de) | Verfahren, um farblose Vinylharze lichtbestaendig zu machen | |
| CH416078A (de) | Makromolekularen organischen Stoff und optischen Aufheller enthaltende Mischung | |
| CH443677A (de) | Verfahren zur Herstellung von Gebilden von verbessertem Aussehen aus Polyoxymethylen oder aus dessen Mischpolymerisaten | |
| DE1288313B (de) | Triazine als flammhemmende Zusatzstoffe | |
| EP0058880B1 (de) | Mischungen von optischen Aufhellern | |
| DE3206091C2 (en]) | ||
| CH616709A5 (en) | Process for spin-dyeing polymers or copolymers of acrylonitrile | |
| DE1695121A1 (de) | v-Triazolyl-cumarine | |
| DE4225665A1 (de) | Modelliermasse | |
| AT208328B (de) | Verfahren zum optischen Aufhellen | |
| DE565980C (de) | Anstrichmittel zum Schutze des Metallbelages von Glasspiegeln | |
| DE1260793B (de) | Verfahren zur Polymerisation von olefinischen ungesaettigten, organischen Verbindungen | |
| DE2059022C3 (de) | Selbstverlöschende Kunststoffmasse | |
| DE1544881A1 (de) | Verfahren zur stufenweisen Haertung von Mischungen aus ungesaettigten Polyestern und anpolymerisierbaren Monomeren | |
| DE1094754B (de) | Verfahren zur Herstellung neuer 1, 3, 4-Oxdiazolverbindungen | |
| DE1802642A1 (de) | Fluoreszierende 1-(Pyrazolinylphenylsulfonyl)-piperazine | |
| CH472463A (de) | Verfahren zum optischen Aufhellen von handelbaren Waschmitteln und hochmolekularem organischem Material mit Ausnahme von nicht-konfektionierten Textilien | |
| DE832146C (de) | Verfahren zur Stabilisierung von technischem Chloral | |
| DE1938014C (de) | 2,3-Dibrom-l,2,4-trichlor-butan und dessen Verwendung | |
| DE1495874A1 (de) | Dentalmaterial | |
| DE842066C (de) | Verfahren zur Herstellung von Phthaloyl-4-chlorchinazolinen | |
| DE1695817A1 (de) | Verfahren zur Herstellung neuer fluoreszierender 1,2,3-Triazolverbindungen des 3-Phenylcumarins |