DE3151814A1 - "fuellstoff enthaltende kunststoff-formmasse, verfahren zu ihrer herstellung sowie deren verwendung" - Google Patents
"fuellstoff enthaltende kunststoff-formmasse, verfahren zu ihrer herstellung sowie deren verwendung"Info
- Publication number
- DE3151814A1 DE3151814A1 DE19813151814 DE3151814A DE3151814A1 DE 3151814 A1 DE3151814 A1 DE 3151814A1 DE 19813151814 DE19813151814 DE 19813151814 DE 3151814 A DE3151814 A DE 3151814A DE 3151814 A1 DE3151814 A1 DE 3151814A1
- Authority
- DE
- Germany
- Prior art keywords
- parts
- carbon atoms
- weight
- alkaline earth
- adhesion promoter
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 239000000945 filler Substances 0.000 title claims abstract description 21
- 238000010137 moulding (plastic) Methods 0.000 title claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000000034 method Methods 0.000 title claims description 7
- -1 polyoxymethylene Polymers 0.000 claims abstract description 76
- 229920006324 polyoxymethylene Polymers 0.000 claims abstract description 36
- 239000002318 adhesion promoter Substances 0.000 claims abstract description 33
- 229930040373 Paraformaldehyde Natural products 0.000 claims abstract description 31
- 239000000203 mixture Substances 0.000 claims abstract description 29
- 238000000465 moulding Methods 0.000 claims abstract description 13
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 64
- 125000004432 carbon atom Chemical group C* 0.000 claims description 28
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 27
- 150000001875 compounds Chemical class 0.000 claims description 24
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 5
- 150000002898 organic sulfur compounds Chemical class 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 229910001413 alkali metal ion Inorganic materials 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 claims description 2
- 239000002253 acid Substances 0.000 abstract description 10
- 229920000642 polymer Polymers 0.000 abstract description 10
- 150000007513 acids Chemical class 0.000 abstract description 9
- 229910052783 alkali metal Inorganic materials 0.000 abstract description 2
- 239000004033 plastic Substances 0.000 abstract description 2
- 229920003023 plastic Polymers 0.000 abstract description 2
- 150000003460 sulfonic acids Chemical class 0.000 abstract description 2
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 239000011159 matrix material Substances 0.000 abstract 1
- 235000010216 calcium carbonate Nutrition 0.000 description 27
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 26
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 10
- 239000011734 sodium Substances 0.000 description 10
- 238000009826 distribution Methods 0.000 description 9
- 239000002245 particle Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 229920001519 homopolymer Polymers 0.000 description 7
- 159000000000 sodium salts Chemical class 0.000 description 7
- 229940088417 precipitated calcium carbonate Drugs 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 6
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 4
- 150000002009 diols Chemical class 0.000 description 4
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- FDCJDKXCCYFOCV-UHFFFAOYSA-N 1-hexadecoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC FDCJDKXCCYFOCV-UHFFFAOYSA-N 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 150000004292 cyclic ethers Chemical class 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 3
- 229920000151 polyglycol Polymers 0.000 description 3
- 239000010695 polyglycol Substances 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
- AUAGGMPIKOZAJZ-UHFFFAOYSA-N 1,3,6-trioxocane Chemical compound C1COCOCCO1 AUAGGMPIKOZAJZ-UHFFFAOYSA-N 0.000 description 2
- CZLMRJZAHXYRIX-UHFFFAOYSA-N 1,3-dioxepane Chemical compound C1CCOCOC1 CZLMRJZAHXYRIX-UHFFFAOYSA-N 0.000 description 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 2
- LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical compound CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 description 2
- ZCQDZFZTCSIQRX-UHFFFAOYSA-N 2-acetyloxydodecane-1-sulfonic acid Chemical compound CCCCCCCCCCC(CS(O)(=O)=O)OC(C)=O ZCQDZFZTCSIQRX-UHFFFAOYSA-N 0.000 description 2
- VRWFADPPHBJBER-UHFFFAOYSA-N 2-hydroxydodecane-1-sulfonic acid Chemical compound CCCCCCCCCCC(O)CS(O)(=O)=O VRWFADPPHBJBER-UHFFFAOYSA-N 0.000 description 2
- YUBGJSHFULOAKN-UHFFFAOYSA-N 2-hydroxyhexadecane-1-sulfonic acid Chemical compound CCCCCCCCCCCCCCC(O)CS(O)(=O)=O YUBGJSHFULOAKN-UHFFFAOYSA-N 0.000 description 2
- ARHQMAACXTXNCM-UHFFFAOYSA-N 2-hydroxytetradecane-1-sulfonic acid Chemical compound CCCCCCCCCCCCC(O)CS(O)(=O)=O ARHQMAACXTXNCM-UHFFFAOYSA-N 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 2
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- FNAQSUUGMSOBHW-UHFFFAOYSA-H calcium citrate Chemical group [Ca+2].[Ca+2].[Ca+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O FNAQSUUGMSOBHW-UHFFFAOYSA-H 0.000 description 2
- 239000001354 calcium citrate Chemical group 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- CCIVGXIOQKPBKL-UHFFFAOYSA-N ethanesulfonic acid Chemical compound CCS(O)(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-N 0.000 description 2
- 238000006266 etherification reaction Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- UIKRCFJTBVTDHX-UHFFFAOYSA-N hexadec-2-ene-1-sulfonic acid Chemical compound CCCCCCCCCCCCCC=CCS(O)(=O)=O UIKRCFJTBVTDHX-UHFFFAOYSA-N 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 150000007517 lewis acids Chemical class 0.000 description 2
- 239000001095 magnesium carbonate Substances 0.000 description 2
- 235000014380 magnesium carbonate Nutrition 0.000 description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N methyl pentane Natural products CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003138 primary alcohols Chemical group 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000009757 thermoplastic moulding Methods 0.000 description 2
- 235000013337 tricalcium citrate Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ORTVZLZNOYNASJ-UPHRSURJSA-N (z)-but-2-ene-1,4-diol Chemical compound OC\C=C/CO ORTVZLZNOYNASJ-UPHRSURJSA-N 0.000 description 1
- NKJOXAZJBOMXID-UHFFFAOYSA-N 1,1'-Oxybisoctane Chemical compound CCCCCCCCOCCCCCCCC NKJOXAZJBOMXID-UHFFFAOYSA-N 0.000 description 1
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical compound C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 description 1
- BQLZNUMAQHULJO-UHFFFAOYSA-N 1,3-dioxonane Chemical compound C1CCCOCOCC1 BQLZNUMAQHULJO-UHFFFAOYSA-N 0.000 description 1
- WDUXFOPUOLGSJU-KHPPLWFESA-N 1-[[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NC(C)S(O)(=O)=O WDUXFOPUOLGSJU-KHPPLWFESA-N 0.000 description 1
- KVGOXGQSTGQXDD-UHFFFAOYSA-N 1-decane-sulfonic-acid Chemical compound CCCCCCCCCCS(O)(=O)=O KVGOXGQSTGQXDD-UHFFFAOYSA-N 0.000 description 1
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 description 1
- NKUBJVWCFAYGAD-UHFFFAOYSA-N 2-(heptadecanoylamino)ethanesulfonic acid Chemical compound CCCCCCCCCCCCCCCCC(=O)NCCS(O)(=O)=O NKUBJVWCFAYGAD-UHFFFAOYSA-N 0.000 description 1
- QYKAWPGWVFEIID-UHFFFAOYSA-N 2-(undecanoylamino)ethanesulfonic acid Chemical compound CCCCCCCCCCC(=O)NCCS(O)(=O)=O QYKAWPGWVFEIID-UHFFFAOYSA-N 0.000 description 1
- HEFGVOBFSXKIKL-KVVVOXFISA-N 2-[(z)-octadec-9-enoyl]oxyethanesulfonic acid;sodium Chemical compound [Na].CCCCCCCC\C=C/CCCCCCCC(=O)OCCS(O)(=O)=O HEFGVOBFSXKIKL-KVVVOXFISA-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
- DZRLZBYMIRXJGO-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxy]ethanol Chemical compound OCCOCCOCC1CO1 DZRLZBYMIRXJGO-UHFFFAOYSA-N 0.000 description 1
- AXGQEJBMPJZXKY-UHFFFAOYSA-N 2-acetyloxytetradecane-1-sulfonic acid Chemical compound CCCCCCCCCCCCC(CS(O)(=O)=O)OC(C)=O AXGQEJBMPJZXKY-UHFFFAOYSA-N 0.000 description 1
- CGXHOLWTAUPTEA-UHFFFAOYSA-N 2-dodecan-2-yloxydodecane Chemical compound CCCCCCCCCCC(C)OC(C)CCCCCCCCCC CGXHOLWTAUPTEA-UHFFFAOYSA-N 0.000 description 1
- UXPUMTCLHVWFKC-UHFFFAOYSA-N 2-dodecanoyloxyethanesulfonic acid Chemical compound CCCCCCCCCCCC(=O)OCCS(O)(=O)=O UXPUMTCLHVWFKC-UHFFFAOYSA-N 0.000 description 1
- GVBHTGJVWDCJHE-UHFFFAOYSA-N 2-heptadecanoyloxyethanesulfonic acid Chemical compound CCCCCCCCCCCCCCCCC(=O)OCCS(O)(=O)=O GVBHTGJVWDCJHE-UHFFFAOYSA-N 0.000 description 1
- ZWDUZVBUHJVJNB-UHFFFAOYSA-N 2-octanoyloxyethanesulfonic acid Chemical class CCCCCCCC(=O)OCCS(O)(=O)=O ZWDUZVBUHJVJNB-UHFFFAOYSA-N 0.000 description 1
- ADLFDNOTASDSPT-UHFFFAOYSA-N 2-tetradecanoyloxyethanesulfonic acid Chemical compound CCCCCCCCCCCCCC(=O)OCCS(O)(=O)=O ADLFDNOTASDSPT-UHFFFAOYSA-N 0.000 description 1
- SMVHGBBQMOOEGG-UHFFFAOYSA-N 2-undecanoyloxyethanesulfonic acid Chemical compound CCCCCCCCCCC(=O)OCCS(O)(=O)=O SMVHGBBQMOOEGG-UHFFFAOYSA-N 0.000 description 1
- IUDNGVFSUHFMCF-UHFFFAOYSA-N 4-(chloromethyl)-1,3-dioxolane Chemical compound ClCC1COCO1 IUDNGVFSUHFMCF-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 229910021630 Antimony pentafluoride Inorganic materials 0.000 description 1
- 239000004135 Bone phosphate Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-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
- 235000019738 Limestone Nutrition 0.000 description 1
- KCFRUUYAXCDZNZ-UHFFFAOYSA-N N-dodecanoyltaurine Chemical class CCCCCCCCCCCC(=O)NCCS(O)(=O)=O KCFRUUYAXCDZNZ-UHFFFAOYSA-N 0.000 description 1
- XPZFMHCHEWYIGE-UHFFFAOYSA-N N-tetradecanoyltaurine Chemical compound CCCCCCCCCCCCCC(=O)NCCS(O)(=O)=O XPZFMHCHEWYIGE-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-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
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-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
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- UMILHIMHKXVDGH-UHFFFAOYSA-N Triethylene glycol diglycidyl ether Chemical compound C1OC1COCCOCCOCCOCC1CO1 UMILHIMHKXVDGH-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
- DLTAKWBTCGPBHI-UHFFFAOYSA-N [Na].CCCCCCCCCCC(=O)OCCS(O)(=O)=O Chemical compound [Na].CCCCCCCCCCC(=O)OCCS(O)(=O)=O DLTAKWBTCGPBHI-UHFFFAOYSA-N 0.000 description 1
- PDEFBLZITZAYNO-UHFFFAOYSA-N [Na].CCCCCCCCCCCCC(CS(O)(=O)=O)OC(C)=O Chemical compound [Na].CCCCCCCCCCCCC(CS(O)(=O)=O)OC(C)=O PDEFBLZITZAYNO-UHFFFAOYSA-N 0.000 description 1
- FAXVAPDWWKNZGV-UHFFFAOYSA-N [Na].CCCCCCCCCCCCCCCCC(=O)OCCS(O)(=O)=O Chemical compound [Na].CCCCCCCCCCCCCCCCC(=O)OCCS(O)(=O)=O FAXVAPDWWKNZGV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001409 amidines Chemical class 0.000 description 1
- VBVBHWZYQGJZLR-UHFFFAOYSA-I antimony pentafluoride Chemical compound F[Sb](F)(F)(F)F VBVBHWZYQGJZLR-UHFFFAOYSA-I 0.000 description 1
- 229940045720 antineoplastic alkylating drug epoxides Drugs 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229960005069 calcium Drugs 0.000 description 1
- 229960004256 calcium citrate Drugs 0.000 description 1
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical group [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 1
- 239000001527 calcium lactate Chemical group 0.000 description 1
- 229960002401 calcium lactate Drugs 0.000 description 1
- 235000011086 calcium lactate Nutrition 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical group [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
- HHSPVTKDOHQBKF-UHFFFAOYSA-J calcium;magnesium;dicarbonate Chemical compound [Mg+2].[Ca+2].[O-]C([O-])=O.[O-]C([O-])=O HHSPVTKDOHQBKF-UHFFFAOYSA-J 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000013256 coordination polymer Substances 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
- 150000005690 diesters Chemical class 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- IRUZVFMAOOLZCM-UHFFFAOYSA-N dodecane-4-sulfonic acid Chemical compound CCCCCCCCC(S(O)(=O)=O)CCC IRUZVFMAOOLZCM-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 229960005237 etoglucid Drugs 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- AKRQHOWXVSDJEF-UHFFFAOYSA-N heptane-1-sulfonic acid Chemical class CCCCCCCS(O)(=O)=O AKRQHOWXVSDJEF-UHFFFAOYSA-N 0.000 description 1
- SSILHZFTFWOUJR-UHFFFAOYSA-N hexadecane-1-sulfonic acid Chemical compound CCCCCCCCCCCCCCCCS(O)(=O)=O SSILHZFTFWOUJR-UHFFFAOYSA-N 0.000 description 1
- GFMIDCCZJUXASS-UHFFFAOYSA-N hexane-1,1,6-triol Chemical compound OCCCCCC(O)O GFMIDCCZJUXASS-UHFFFAOYSA-N 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- FYAQQULBLMNGAH-UHFFFAOYSA-N hexane-1-sulfonic acid Chemical class CCCCCCS(O)(=O)=O FYAQQULBLMNGAH-UHFFFAOYSA-N 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000003116 impacting effect Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- TXSUIVPRHHQNTM-UHFFFAOYSA-N n'-(3-methylanilino)-n-phenyliminobenzenecarboximidamide Chemical group CC1=CC=CC(NN=C(N=NC=2C=CC=CC=2)C=2C=CC=CC=2)=C1 TXSUIVPRHHQNTM-UHFFFAOYSA-N 0.000 description 1
- AXWCIZPJQUQIIX-UHFFFAOYSA-N nonane-2-sulfonic acid Chemical class CCCCCCCC(C)S(O)(=O)=O AXWCIZPJQUQIIX-UHFFFAOYSA-N 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- CACRRXGTWZXOAU-UHFFFAOYSA-N octadecane-1-sulfonic acid Chemical compound CCCCCCCCCCCCCCCCCCS(O)(=O)=O CACRRXGTWZXOAU-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- WLGDAKIJYPIYLR-UHFFFAOYSA-N octane-1-sulfonic acid Chemical class CCCCCCCCS(O)(=O)=O WLGDAKIJYPIYLR-UHFFFAOYSA-N 0.000 description 1
- LHQXHHDBJMMPCQ-UHFFFAOYSA-N octane-2-sulfonic acid Chemical class CCCCCCC(C)S(O)(=O)=O LHQXHHDBJMMPCQ-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- NAHIZHJHSUSESF-UHFFFAOYSA-N perchloryl acetate Chemical compound CC(=O)OCl(=O)(=O)=O NAHIZHJHSUSESF-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003196 poly(1,3-dioxolane) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 125000000075 primary alcohol group Chemical group 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- WKQSAIMSWSDTIX-UHFFFAOYSA-M sodium hexadec-2-ene-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCCC=CCS([O-])(=O)=O WKQSAIMSWSDTIX-UHFFFAOYSA-M 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- MYOWBHNETUSQPA-UHFFFAOYSA-N tetradecane-1-sulfonic acid Chemical compound CCCCCCCCCCCCCCS(O)(=O)=O MYOWBHNETUSQPA-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- SJEYEFOHSMBQIX-UHFFFAOYSA-N undecane-1-sulfonic acid Chemical compound CCCCCCCCCCCS(O)(=O)=O SJEYEFOHSMBQIX-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000001291 vacuum drying 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; Derivatives thereof
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 (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813151814 DE3151814A1 (de) | 1981-12-29 | 1981-12-29 | "fuellstoff enthaltende kunststoff-formmasse, verfahren zu ihrer herstellung sowie deren verwendung" |
| US06/449,160 US4456710A (en) | 1981-12-29 | 1982-12-13 | Filler-containing plastic molding composition, a process for its preparation, and its use |
| AT82111956T ATE19260T1 (de) | 1981-12-29 | 1982-12-23 | Fuellstoff enthaltende kunststoff-formmasse, verfahren zu ihrer herstellung sowie deren verwendung. |
| EP82111956A EP0083084B1 (de) | 1981-12-29 | 1982-12-23 | Füllstoff enthaltende Kunststoff-Formmasse, Verfahren zu ihrer Herstellung sowie deren Verwendung |
| DE8282111956T DE3270693D1 (en) | 1981-12-29 | 1982-12-23 | Polymer moulding composition containing a filler, process for its preparation and its use |
| CA000418454A CA1205941A (en) | 1981-12-29 | 1982-12-23 | Filler-containing plastic molding composition, a process for its preparation, and its use |
| JP57227185A JPS58118844A (ja) | 1981-12-29 | 1982-12-27 | 填料含有合成樹脂成形用組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813151814 DE3151814A1 (de) | 1981-12-29 | 1981-12-29 | "fuellstoff enthaltende kunststoff-formmasse, verfahren zu ihrer herstellung sowie deren verwendung" |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE3151814A1 true DE3151814A1 (de) | 1983-07-07 |
Family
ID=6149958
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19813151814 Withdrawn DE3151814A1 (de) | 1981-12-29 | 1981-12-29 | "fuellstoff enthaltende kunststoff-formmasse, verfahren zu ihrer herstellung sowie deren verwendung" |
| DE8282111956T Expired DE3270693D1 (en) | 1981-12-29 | 1982-12-23 | Polymer moulding composition containing a filler, process for its preparation and its use |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE8282111956T Expired DE3270693D1 (en) | 1981-12-29 | 1982-12-23 | Polymer moulding composition containing a filler, process for its preparation and its use |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4456710A (https=) |
| EP (1) | EP0083084B1 (https=) |
| JP (1) | JPS58118844A (https=) |
| AT (1) | ATE19260T1 (https=) |
| CA (1) | CA1205941A (https=) |
| DE (2) | DE3151814A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0115846A2 (de) | 1983-02-04 | 1984-08-15 | Hoechst Aktiengesellschaft | Schlagzäh modifiziertes Polyoxymethylen und daraus hergestellte Formkörper |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4954545A (en) * | 1987-07-27 | 1990-09-04 | Phillips Petroleum Company | Process for cleaning polymer processing equipment |
| GB8724959D0 (en) * | 1987-10-24 | 1987-11-25 | Dow Corning Sa | Filled compositions |
| GB8724958D0 (en) * | 1987-10-24 | 1987-11-25 | Dow Corning Sa | Filled compositions & additives |
| US5156913A (en) * | 1989-12-11 | 1992-10-20 | Hoechst Celanese Corp. | Glass reinforced acetal polymer products |
| US5773503A (en) * | 1996-12-11 | 1998-06-30 | Luzenac America, Inc. | Compacted mineral filler pellet and method for making the same |
| US6815479B1 (en) * | 1999-02-19 | 2004-11-09 | E. I. Du Pont De Nemours And Company | Toughened high modulus mineral filled polyoxymethylene polymers |
| WO2002014429A1 (en) * | 2000-08-17 | 2002-02-21 | E.I. Du Pont De Nemours And Company | Toughened, high-modulus polyacetals |
| DE10047488B4 (de) * | 2000-09-26 | 2006-12-07 | Ticona Gmbh | Eingefärbte Polyoxymethylen-Formmassen und daraus hergestellte Formteile |
| WO2002026885A1 (de) * | 2000-09-26 | 2002-04-04 | Ticona Gmbh | Eingefärbte polyoxymethylen-formmassen und daraus hergestellte formteile |
| US20040242747A1 (en) * | 2003-05-30 | 2004-12-02 | Malay Nandi | Polyoxymethylene homopolymer with improved thermal stability |
| WO2005071011A1 (ja) * | 2004-01-21 | 2005-08-04 | Asahi Kasei Chemicals Corporation | ポリアセタール樹脂組成物 |
| JP4730948B2 (ja) * | 2005-08-03 | 2011-07-20 | 旭化成ケミカルズ株式会社 | ポリアセタール樹脂組成物 |
| US8631583B2 (en) | 2005-10-31 | 2014-01-21 | Dennis Moss | Bagel slicer |
| US20080127497A1 (en) * | 2005-10-31 | 2008-06-05 | Dennis Moss | Blade assembly |
| EP2036944A1 (en) * | 2007-09-14 | 2009-03-18 | SOLVAY (Société Anonyme) | Polymer compositions |
| US9061920B2 (en) * | 2009-11-10 | 2015-06-23 | Omya International Ag | Precipitated magnesium carbonate |
| EP2390285A1 (en) | 2010-05-28 | 2011-11-30 | Omya Development AG | Process for the preparation of surface treated mineral filler products and uses of same |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2841504A (en) * | 1953-09-01 | 1958-07-01 | Wyandotte Chemicals Corp | Surface coated calcium carbonate pigments |
| GB1025675A (en) * | 1962-06-06 | 1966-04-14 | Celanese Corp | Surface treatment of oxymethylene polymers |
| DE1220129B (de) * | 1963-10-25 | 1966-06-30 | Hoechst Ag | Verfahren zur Oberflaechenbehandlung von Polyacetal-Formkoerpern |
| DE2538954A1 (de) * | 1975-09-02 | 1977-03-10 | Hoechst Ag | Verfahren zur herstellung von oxymethylenpolymeren |
| DE2735160A1 (de) * | 1977-08-04 | 1979-02-22 | Hoechst Ag | Fuellstoff enthaltende kunststoff- formmasse |
| DE2818240A1 (de) * | 1978-04-26 | 1979-11-08 | Hoechst Ag | Thermoplastische formmassen auf basis von polyoxymethylenen |
| US4274987A (en) * | 1978-09-11 | 1981-06-23 | Nl Industries, Inc. | Coupling agents for thermoplastic composites |
| JPS5919588B2 (ja) * | 1978-09-27 | 1984-05-07 | ライオン株式会社 | 無臭性樹脂組成物 |
| DE2910586B2 (de) * | 1979-03-17 | 1981-01-29 | Hoechst Ag, 6000 Frankfurt | Füllstoff enthaltende Polyolefin-Formmasse und Verfahren zu ihrer Herstellung |
| US4274995A (en) * | 1979-12-31 | 1981-06-23 | Stauffer Chemical Company | Filled polyolefin compositions having improved thermal stability |
-
1981
- 1981-12-29 DE DE19813151814 patent/DE3151814A1/de not_active Withdrawn
-
1982
- 1982-12-13 US US06/449,160 patent/US4456710A/en not_active Expired - Fee Related
- 1982-12-23 CA CA000418454A patent/CA1205941A/en not_active Expired
- 1982-12-23 AT AT82111956T patent/ATE19260T1/de not_active IP Right Cessation
- 1982-12-23 DE DE8282111956T patent/DE3270693D1/de not_active Expired
- 1982-12-23 EP EP82111956A patent/EP0083084B1/de not_active Expired
- 1982-12-27 JP JP57227185A patent/JPS58118844A/ja active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0115846A2 (de) | 1983-02-04 | 1984-08-15 | Hoechst Aktiengesellschaft | Schlagzäh modifiziertes Polyoxymethylen und daraus hergestellte Formkörper |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1205941A (en) | 1986-06-10 |
| US4456710A (en) | 1984-06-26 |
| DE3270693D1 (en) | 1986-05-22 |
| EP0083084B1 (de) | 1986-04-16 |
| EP0083084A2 (de) | 1983-07-06 |
| JPH0326222B2 (https=) | 1991-04-10 |
| ATE19260T1 (de) | 1986-05-15 |
| EP0083084A3 (en) | 1984-01-11 |
| JPS58118844A (ja) | 1983-07-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0083084B1 (de) | Füllstoff enthaltende Kunststoff-Formmasse, Verfahren zu ihrer Herstellung sowie deren Verwendung | |
| EP0004973B1 (de) | Thermoplastische Formmassen auf Basis von Polyoxymethylenen | |
| EP0115846B2 (de) | Schlagzäh modifiziertes Polyoxymethylen und daraus hergestellte Formkörper | |
| EP0115847B1 (de) | Schlagzäh modifiziertes Polyoxymethylen und daraus hergestellte Formkörper | |
| CH618717A5 (https=) | ||
| EP0017038A1 (de) | Füllstoff enthaltende Kunststoff-Formmasse und Verfahren zu ihrer Herstellung | |
| EP0789049A1 (de) | Antistatisch ausgerüstete Polymere | |
| DE2646965A1 (de) | Anorganischer fuellstoff und damit gefuellte kunstharzmasse | |
| EP0008046B1 (de) | Stabilisierte Polyalkylenterephthalat-Formmassen und ihre Verwendung zur Herstellung von Formkörpern, Folien, Monofilen und Fasern | |
| EP0164667B1 (de) | Thermoplastische Formmassen auf der Basis von Polyoxymethylen und polymeren Adipatcarbonatmischestern | |
| DE1195490B (de) | Stabilisatoren fuer Polyoxymethylene | |
| DE4031794C1 (https=) | ||
| DE60012950T2 (de) | Polyacetalharzzusammensetzung | |
| DE2735946C3 (de) | Körniges Oxymethylenpolymer mit verbesserten mechanischen Eigenschaften und Verfahren zu dessen Herstellung | |
| DE4235958A1 (de) | Polyoxymethylen mit verbesserter Stabilität gegen Säuren, Verfahren zu seiner Herstellung sowie Verwendung | |
| EP0381943A2 (de) | Polyoxymethylen-Formmasse | |
| DE1669834C3 (de) | Thermoplastische Formmassen mit verbesserter Schlagzähigkeit | |
| DE2037823C3 (de) | Thermoplastische Formmassen auf Polyoxymethylenbasis | |
| DE4433667C1 (de) | Polyoxymethylen mit verbesserter Stabilität gegen Zink- und/oder Kupferionen sowie Verfahren zu seiner Herstellung und Weiterverarbeitung zu Formteilen | |
| DE1298716B (de) | Polyoxymethylen-Pressmassen | |
| DE4412366A1 (de) | Antistatisch ausgerüstete Kunststoff-Formmasse | |
| DE2540206B1 (de) | Polyoxymethylen-Formmassen (II) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8139 | Disposal/non-payment of the annual fee |