JPS58118844A - 填料含有合成樹脂成形用組成物 - Google Patents

填料含有合成樹脂成形用組成物

Info

Publication number: JPS58118844A
Authority: JP; Japan
Prior art keywords: carbon atoms; parts; alkyl group; weight; alkaline earth
Prior art date: 1981-12-29
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.): Granted

Application number

JP57227185A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0326222B2 (2

Inventor

ウアルテル・リユ−デルス

カルルハインツ・ブルク

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Hoechst AG

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.)

1981-12-29

Filing date

1982-12-27

Publication date

1983-07-15

1982-12-27 Application filed by Hoechst AG filed Critical Hoechst AG

1983-07-15 Publication of JPS58118844A publication Critical patent/JPS58118844A/ja

1991-04-10 Publication of JPH0326222B2 publication Critical patent/JPH0326222B2/ja

Status Granted legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims description 42
239000000945 filler Substances 0.000 title claims description 16
229920003002 synthetic resin Polymers 0.000 title claims description 6
239000000057 synthetic resin Substances 0.000 title claims description 6
238000004519 manufacturing process Methods 0.000 title claims description 5
-1 polyoxymethylene Polymers 0.000 claims description 60
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical group [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 49
125000004432 carbon atom Chemical group C* 0.000 claims description 36
229920006324 polyoxymethylene Polymers 0.000 claims description 30
239000002318 adhesion promoter Substances 0.000 claims description 28
229930040373 Paraformaldehyde Natural products 0.000 claims description 27
229910000019 calcium carbonate Inorganic materials 0.000 claims description 22
238000000465 moulding Methods 0.000 claims description 19
125000000217 alkyl group Chemical group 0.000 claims description 18
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 13
239000000654 additive Substances 0.000 claims description 6
125000003342 alkenyl group Chemical group 0.000 claims description 6
239000011593 sulfur Substances 0.000 claims description 5
229910052717 sulfur Inorganic materials 0.000 claims description 5
229910052783 alkali metal Inorganic materials 0.000 claims description 4
150000001340 alkali metals Chemical class 0.000 claims description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
229910001420 alkaline earth metal ion Inorganic materials 0.000 claims description 3
125000002877 alkyl aryl group Chemical group 0.000 claims description 3
229910052799 carbon Inorganic materials 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
229910001413 alkali metal ion Inorganic materials 0.000 claims description 2
125000004965 chloroalkyl group Chemical group 0.000 claims 1
125000001475 halogen functional group Chemical group 0.000 claims 1
150000001875 compounds Chemical class 0.000 description 16
230000000052 comparative effect Effects 0.000 description 13
229920000642 polymer Polymers 0.000 description 11
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
229920001577 copolymer Polymers 0.000 description 10
238000009826 distribution Methods 0.000 description 9
239000002245 particle Substances 0.000 description 8
238000012805 post-processing Methods 0.000 description 8
239000002253 acid Substances 0.000 description 7
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 6
238000002156 mixing Methods 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Substances OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
229920001519 homopolymer Polymers 0.000 description 5
239000000178 monomer Substances 0.000 description 5
229940088417 precipitated calcium carbonate Drugs 0.000 description 5
239000011734 sodium Substances 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
159000000000 sodium salts Chemical class 0.000 description 5
150000003467 sulfuric acid derivatives Chemical class 0.000 description 5
BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 4
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
GXGJIOMUZAGVEH-UHFFFAOYSA-N Chamazulene Chemical group CCC1=CC=C(C)C2=CC=C(C)C2=C1 GXGJIOMUZAGVEH-UHFFFAOYSA-N 0.000 description 4
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 4
208000000474 Poliomyelitis Diseases 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
239000011575 calcium Substances 0.000 description 4
229910052791 calcium Inorganic materials 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000007921 spray Substances 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
150000001335 aliphatic alkanes Chemical class 0.000 description 3
150000002009 diols Chemical class 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
238000011068 loading method Methods 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
239000000843 powder Substances 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
239000000243 solution Substances 0.000 description 3
LDMOEFOXLIZJOW-UHFFFAOYSA-N 1-dodecanesulfonic acid Chemical compound CCCCCCCCCCCCS(O)(=O)=O LDMOEFOXLIZJOW-UHFFFAOYSA-N 0.000 description 2
HANWHVWXFQSQGJ-UHFFFAOYSA-N 1-tetradecoxytetradecane Chemical compound CCCCCCCCCCCCCCOCCCCCCCCCCCCCC HANWHVWXFQSQGJ-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
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
239000002841 Lewis acid Substances 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
239000003513 alkali Chemical class 0.000 description 2
239000002585 base Substances 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000005520 cutting process Methods 0.000 description 2
150000004292 cyclic ethers Chemical class 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
230000006866 deterioration Effects 0.000 description 2
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
230000032050 esterification Effects 0.000 description 2
238000005886 esterification reaction Methods 0.000 description 2
238000006266 etherification reaction Methods 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Substances OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
238000002347 injection Methods 0.000 description 2
239000007924 injection Substances 0.000 description 2
238000001746 injection moulding Methods 0.000 description 2
150000007517 lewis acids Chemical class 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 2
239000001095 magnesium carbonate Substances 0.000 description 2
229910000021 magnesium carbonate Inorganic materials 0.000 description 2
235000014380 magnesium carbonate Nutrition 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
238000007254 oxidation reaction Methods 0.000 description 2
125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 2
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
239000011591 potassium Substances 0.000 description 2
229910052700 potassium Inorganic materials 0.000 description 2
238000012545 processing Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
SFXOHDOEOSCUCT-UHFFFAOYSA-N styrene;hydrochloride Chemical compound Cl.C=CC1=CC=CC=C1 SFXOHDOEOSCUCT-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
150000003460 sulfonic acids Chemical class 0.000 description 2
238000009757 thermoplastic moulding Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
BQLZNUMAQHULJO-UHFFFAOYSA-N 1,3-dioxonane Chemical compound C1CCCOCOCC1 BQLZNUMAQHULJO-UHFFFAOYSA-N 0.000 description 1
LMTDPKYREUZYAO-UHFFFAOYSA-N 1,4-dioxepane Chemical compound C1COCCOC1 LMTDPKYREUZYAO-UHFFFAOYSA-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
LTSWUFKUZPPYEG-UHFFFAOYSA-N 1-decoxydecane Chemical compound CCCCCCCCCCOCCCCCCCCCC LTSWUFKUZPPYEG-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
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
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
SMVHGBBQMOOEGG-UHFFFAOYSA-N 2-undecanoyloxyethanesulfonic acid Chemical compound CCCCCCCCCCC(=O)OCCS(O)(=O)=O SMVHGBBQMOOEGG-UHFFFAOYSA-N 0.000 description 1
HKCCZYKCEQAFNJ-UHFFFAOYSA-N 74835-82-8 Chemical compound F.F.F.F.F.F.F HKCCZYKCEQAFNJ-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
235000002568 Capsicum frutescens Nutrition 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
101100136092 Drosophila melanogaster peng gene Proteins 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
241001547860 Gaya Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
YQEZLKZALYSWHR-UHFFFAOYSA-N Ketamine Chemical compound C=1C=CC=C(Cl)C=1C1(NC)CCCCC1=O YQEZLKZALYSWHR-UHFFFAOYSA-N 0.000 description 1
235000019738 Limestone Nutrition 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
AFVFQIVMOAPDHO-UHFFFAOYSA-M Methanesulfonate Chemical compound CS([O-])(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 description 1
QHYZICICAOBWPZ-UHFFFAOYSA-N O=S(=O)=S(=O)=O Chemical compound O=S(=O)=S(=O)=O QHYZICICAOBWPZ-UHFFFAOYSA-N 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical class C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 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
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-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
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-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
150000001241 acetals Chemical class 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
150000001342 alkaline earth metals Chemical group 0.000 description 1
229940045720 antineoplastic alkylating drug epoxides Drugs 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000006399 behavior Effects 0.000 description 1
125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
125000006267 biphenyl group Chemical group 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
235000012241 calcium silicate Nutrition 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
235000012730 carminic acid Nutrition 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000008395 clarifying agent Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical compound CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
TXKMVPPZCYKFAC-UHFFFAOYSA-N disulfur monoxide Inorganic materials O=S=S TXKMVPPZCYKFAC-UHFFFAOYSA-N 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
230000000694 effects Effects 0.000 description 1
150000002118 epoxides Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
KDKYADYSIPSCCQ-UHFFFAOYSA-N ethyl acetylene Natural products CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 description 1
229960005237 etoglucid Drugs 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
230000004634 feeding behavior Effects 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
AKRQHOWXVSDJEF-UHFFFAOYSA-N heptane-1-sulfonic acid Chemical compound CCCCCCCS(O)(=O)=O AKRQHOWXVSDJEF-UHFFFAOYSA-N 0.000 description 1
UIKRCFJTBVTDHX-UHFFFAOYSA-N hexadec-2-ene-1-sulfonic acid Chemical compound CCCCCCCCCCCCCC=CCS(O)(=O)=O UIKRCFJTBVTDHX-UHFFFAOYSA-N 0.000 description 1
238000000265 homogenisation Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 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
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000000463 material Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000007769 metal material Substances 0.000 description 1
DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
AXWCIZPJQUQIIX-UHFFFAOYSA-N nonane-2-sulfonic acid Chemical compound CCCCCCCC(C)S(O)(=O)=O AXWCIZPJQUQIIX-UHFFFAOYSA-N 0.000 description 1
ARDSQJLUSITVJA-UHFFFAOYSA-N nonane-5-sulfonic acid Chemical compound CCCCC(S(O)(=O)=O)CCCC ARDSQJLUSITVJA-UHFFFAOYSA-N 0.000 description 1
239000002667 nucleating agent Substances 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 compound CCCCCCCCS(O)(=O)=O WLGDAKIJYPIYLR-UHFFFAOYSA-N 0.000 description 1
LHQXHHDBJMMPCQ-UHFFFAOYSA-N octane-2-sulfonic acid Chemical compound CCCCCCC(C)S(O)(=O)=O LHQXHHDBJMMPCQ-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000001282 organosilanes Chemical class 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
150000003138 primary alcohols Chemical group 0.000 description 1
239000000047 product Substances 0.000 description 1
210000004767 rumen Anatomy 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
229910001415 sodium ion Inorganic materials 0.000 description 1
YRYGQUYZXADJLY-UHFFFAOYSA-M sodium;2-hydroxydodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCC(O)CS([O-])(=O)=O YRYGQUYZXADJLY-UHFFFAOYSA-M 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
210000002784 stomach Anatomy 0.000 description 1
239000004575 stone Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
238000006277 sulfonation reaction Methods 0.000 description 1
XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
239000000725 suspension Substances 0.000 description 1
MYOWBHNETUSQPA-UHFFFAOYSA-N tetradecane-1-sulfonic acid Chemical compound CCCCCCCCCCCCCCS(O)(=O)=O MYOWBHNETUSQPA-UHFFFAOYSA-N 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
238000001291 vacuum drying Methods 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000010792 warming Methods 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
- 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)

JP57227185A 1981-12-29 1982-12-27 填料含有合成樹脂成形用組成物 Granted JPS58118844A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3151814.1		1981-12-29
DE19813151814 DE3151814A1 (de)	1981-12-29	1981-12-29	"fuellstoff enthaltende kunststoff-formmasse, verfahren zu ihrer herstellung sowie deren verwendung"

Publications (2)

Publication Number	Publication Date
JPS58118844A true JPS58118844A (ja)	1983-07-15
JPH0326222B2 JPH0326222B2 (2)	1991-04-10

Family

ID=6149958

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP57227185A Granted JPS58118844A (ja)	1981-12-29	1982-12-27	填料含有合成樹脂成形用組成物

Country Status (6)

Country	Link
US (1)	US4456710A (2)
EP (1)	EP0083084B1 (2)
JP (1)	JPS58118844A (2)
AT (1)	ATE19260T1 (2)
CA (1)	CA1205941A (2)
DE (2)	DE3151814A1 (2)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2007039545A (ja) *	2005-08-03	2007-02-15	Asahi Kasei Chemicals Corp	ポリアセタール樹脂組成物

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3303760A1 (de)	1983-02-04	1984-08-09	Hoechst Ag, 6230 Frankfurt	Schlagzaeh modifiziertes polyoxymethylen und daraus hergestellte formkoerper
US4954545A (en) *	1987-07-27	1990-09-04	Phillips Petroleum Company	Process for cleaning polymer processing equipment
GB8724958D0 (en) *	1987-10-24	1987-11-25	Dow Corning Sa	Filled compositions & additives
GB8724959D0 (en) *	1987-10-24	1987-11-25	Dow Corning Sa	Filled compositions
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
JP2004506772A (ja) *	2000-08-17	2004-03-04	イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー	強化された高弾性ポリアセタール
ATE319774T1 (de) *	2000-09-26	2006-03-15	Ticona Gmbh	Eingefärbte polyoxymethylen-formmassen und daraus hergestellte formteile
DE10047488B4 (de) *	2000-09-26	2006-12-07	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
US20080127497A1 (en) *	2005-10-31	2008-06-05	Dennis Moss	Blade assembly
US8631583B2 (en)	2005-10-31	2014-01-21	Dennis Moss	Bagel slicer
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)

* Cited by examiner, † Cited by third party
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 AT AT82111956T patent/ATE19260T1/de not_active IP Right Cessation
- 1982-12-23 CA CA000418454A patent/CA1205941A/en not_active Expired
- 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)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2007039545A (ja) *	2005-08-03	2007-02-15	Asahi Kasei Chemicals Corp	ポリアセタール樹脂組成物

Also Published As

Publication number	Publication date
CA1205941A (en)	1986-06-10
DE3151814A1 (de)	1983-07-07
ATE19260T1 (de)	1986-05-15
EP0083084A3 (en)	1984-01-11
JPH0326222B2 (2)	1991-04-10
US4456710A (en)	1984-06-26
DE3270693D1 (en)	1986-05-22
EP0083084A2 (de)	1983-07-06
EP0083084B1 (de)	1986-04-16

Publication	Publication Date	Title
JPS58118844A (ja)	1983-07-15	填料含有合成樹脂成形用組成物
US3634543A (en)	1972-01-11	Nucleated graft polymers of polycaprolactam on carboxy containing copolymeric backbone
US3305605A (en)	1967-02-21	Compositions containing polycarbonate plasticizers
DE3752171T2 (de)	1998-07-30	Polyesterharzzusammensetzung
US3813358A (en)	1974-05-28	Polycarbonate molding composition comprising an aromatic polycarbonate graft copolymer and a modifier
JPH0439496B2 (2)	1992-06-29
JPS6019331B2 (ja)	1985-05-15	オキシメチレン重合体を主体とする成形用組成物およびその製造方法
US4092296A (en)	1978-05-30	Epoxy resin compositions
US3980734A (en)	1976-09-14	Thermoplastic moulding compositions based on poly (oxymethylene)
PL80934B1 (en)	1975-08-30	Thermoplastic molding compositions on the basis of polyoxymethylenes[us3704275a]
US4965300A (en)	1990-10-23	Sequential copolymers based on cyclic carbonates and esters
DE2012012A1 (2)	1970-10-08
EP0691336A1 (fr)	1996-01-10	Nouveaux agents dispersants dérivés d'anhydride et nouvelles compositions polymériques chargées ainsi que leurs applications
US4065401A (en)	1977-12-27	Blowing agent mixture
US3637553A (en)	1972-01-25	Production of homogeneous thermoplastic and highly elastic plastics from vinyl chloride polymers and polyurethanes
JPS5966457A (ja)	1984-04-14	成形または未成形のプラスチツク用安定剤
DE1252898B (de)	1967-10-26	Verfahren zur Herstellung von Copolymerisaten des Trioxans
DE68922962T2 (de)	1995-10-19	Thermoplastische Formmasse und Verfahren zu deren Herstellung.
JPS6136325A (ja)	1986-02-21	重合体親水物およびその製造方法
JPH03223322A (ja)	1991-10-02	ポリアセタール共重合体及びその組成物
US3170887A (en)	1965-02-23	Method of making same
JPS62116656A (ja)	1987-05-28	ポリカ−ボネ−ト樹脂およびエチレンとアクリル酸またはメタクリル酸とのコポリマ−からなる熱可塑性組成物
JPH02191606A (ja)	1990-07-27	反応性ポリ塩化ビニルおよびこれから製造したポリマー製品
US3836605A (en)	1974-09-17	Polycondensates of diamides,n,n'-ureas and formaldehyde admixed with oxymethylene polymers
US3487452A (en)	1969-12-30	Alkenylsuccinic amide-lactones

JPS58118844A - 填料含有合成樹脂成形用組成物 - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (2)

Publications (2)

Family

ID=6149958

Family Applications (1)

Country Status (6)

Cited By (1)

Families Citing this family (17)

Family Cites Families (10)

Cited By (1)

Also Published As

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