KR20140146160A - 폴리에테르이미드, 이의 제조방법 및 이로부터 형성된 물품 - Google Patents
폴리에테르이미드, 이의 제조방법 및 이로부터 형성된 물품 Download PDFInfo
- Publication number
- KR20140146160A KR20140146160A KR1020147030669A KR20147030669A KR20140146160A KR 20140146160 A KR20140146160 A KR 20140146160A KR 1020147030669 A KR1020147030669 A KR 1020147030669A KR 20147030669 A KR20147030669 A KR 20147030669A KR 20140146160 A KR20140146160 A KR 20140146160A
- Authority
- KR
- South Korea
- Prior art keywords
- polyetherimide
- alkali metal
- formula
- composition
- less
- 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.)
- Abandoned
Links
- 229920001601 polyetherimide Polymers 0.000 title claims abstract description 261
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 12
- 238000000034 method Methods 0.000 title claims description 64
- 239000004697 Polyetherimide Substances 0.000 claims abstract description 249
- 239000000203 mixture Substances 0.000 claims abstract description 173
- -1 alkali metal salt Chemical class 0.000 claims abstract description 158
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 97
- 150000001491 aromatic compounds Chemical class 0.000 claims abstract description 30
- 239000000155 melt Substances 0.000 claims abstract description 19
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims abstract description 17
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 14
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 65
- 239000011734 sodium Substances 0.000 claims description 61
- 125000003118 aryl group Chemical group 0.000 claims description 34
- 239000003054 catalyst Substances 0.000 claims description 30
- 239000000945 filler Substances 0.000 claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 28
- 239000000654 additive Substances 0.000 claims description 26
- 150000004985 diamines Chemical class 0.000 claims description 26
- 150000008064 anhydrides Chemical class 0.000 claims description 23
- 239000000835 fiber Substances 0.000 claims description 20
- QBDSZLJBMIMQRS-UHFFFAOYSA-N p-Cumylphenol Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=CC=C1 QBDSZLJBMIMQRS-UHFFFAOYSA-N 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 230000008569 process Effects 0.000 claims description 17
- 125000005843 halogen group Chemical group 0.000 claims description 16
- NKTOLZVEWDHZMU-UHFFFAOYSA-N p-cumyl phenol Natural products CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 claims description 16
- 239000003963 antioxidant agent Substances 0.000 claims description 15
- 150000001340 alkali metals Chemical class 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 13
- 229910052708 sodium Inorganic materials 0.000 claims description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 12
- 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 claims description 12
- 239000006082 mold release agent Substances 0.000 claims description 11
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 10
- 230000000996 additive effect Effects 0.000 claims description 10
- 239000012763 reinforcing filler Substances 0.000 claims description 10
- 239000002904 solvent Substances 0.000 claims description 10
- APOAEMIYHVGWEZ-UHFFFAOYSA-N 4-chloroisoindole-1,3-dione Chemical compound ClC1=CC=CC2=C1C(=O)NC2=O APOAEMIYHVGWEZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000000843 powder Substances 0.000 claims description 9
- 239000003381 stabilizer Substances 0.000 claims description 9
- 238000000576 coating method Methods 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- 125000002950 monocyclic group Chemical group 0.000 claims description 8
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 7
- 125000001246 bromo group Chemical group Br* 0.000 claims description 7
- 125000002346 iodo group Chemical group I* 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 7
- 239000002184 metal Substances 0.000 claims description 7
- 238000000465 moulding Methods 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 7
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical class [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 6
- 238000001125 extrusion Methods 0.000 claims description 6
- 239000004611 light stabiliser Substances 0.000 claims description 6
- 159000000000 sodium salts Chemical class 0.000 claims description 6
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 5
- 239000004744 fabric Substances 0.000 claims description 5
- 239000006260 foam Substances 0.000 claims description 5
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 claims description 5
- 239000002966 varnish Substances 0.000 claims description 5
- 239000012760 heat stabilizer Substances 0.000 claims description 4
- 229910003002 lithium salt Inorganic materials 0.000 claims description 4
- 159000000002 lithium salts Chemical class 0.000 claims description 4
- 239000000314 lubricant Substances 0.000 claims description 4
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims description 4
- 238000007493 shaping process Methods 0.000 claims description 4
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 claims description 3
- 239000004609 Impact Modifier Substances 0.000 claims description 3
- 230000003078 antioxidant effect Effects 0.000 claims description 3
- 239000004014 plasticizer Substances 0.000 claims description 3
- 230000005855 radiation Effects 0.000 claims description 3
- 238000009987 spinning Methods 0.000 claims description 3
- 238000003856 thermoforming Methods 0.000 claims description 3
- 238000009941 weaving Methods 0.000 claims description 2
- 239000006096 absorbing agent Substances 0.000 claims 1
- 150000005690 diesters Chemical class 0.000 claims 1
- 239000012744 reinforcing agent Substances 0.000 claims 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 abstract description 26
- 239000000460 chlorine Substances 0.000 abstract description 21
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract description 10
- 229910052801 chlorine Inorganic materials 0.000 abstract description 10
- 229920000642 polymer Polymers 0.000 description 67
- 238000006116 polymerization reaction Methods 0.000 description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 38
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 36
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 33
- LYWKAJZTPLXHEM-UHFFFAOYSA-M bis(diethylamino)methylidene-diethylazanium;chloride Chemical compound [Cl-].CCN(CC)C(N(CC)CC)=[N+](CC)CC LYWKAJZTPLXHEM-UHFFFAOYSA-M 0.000 description 32
- 239000002002 slurry Substances 0.000 description 30
- 239000007787 solid Substances 0.000 description 30
- 230000000052 comparative effect Effects 0.000 description 29
- 239000000178 monomer Substances 0.000 description 22
- 239000000243 solution Substances 0.000 description 21
- 229910052757 nitrogen Inorganic materials 0.000 description 18
- 239000000049 pigment Substances 0.000 description 18
- 238000010438 heat treatment Methods 0.000 description 14
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 10
- 229920004738 ULTEM® Polymers 0.000 description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 9
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 9
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 9
- 229910052736 halogen Inorganic materials 0.000 description 9
- 238000004128 high performance liquid chromatography Methods 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 8
- 229920002313 fluoropolymer Polymers 0.000 description 8
- 239000004811 fluoropolymer Substances 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 239000000523 sample Substances 0.000 description 8
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 7
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 7
- 229920001577 copolymer Polymers 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 6
- 239000005995 Aluminium silicate Substances 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 235000012211 aluminium silicate Nutrition 0.000 description 6
- 239000002131 composite material Substances 0.000 description 6
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 6
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 229920000098 polyolefin Polymers 0.000 description 6
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 238000003109 Karl Fischer titration Methods 0.000 description 5
- 239000004642 Polyimide Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 5
- 229910052794 bromium Inorganic materials 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 125000004122 cyclic group Chemical group 0.000 description 5
- 239000012765 fibrous filler Substances 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 150000003949 imides Chemical class 0.000 description 5
- 238000001746 injection moulding Methods 0.000 description 5
- 238000003760 magnetic stirring Methods 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- 239000003444 phase transfer catalyst Substances 0.000 description 5
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 5
- 229910052698 phosphorus Chemical group 0.000 description 5
- 239000011574 phosphorus Chemical group 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
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- 229920001721 polyimide Polymers 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
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- MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 229920004748 ULTEM® 1010 Polymers 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229940106691 bisphenol a Drugs 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
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- 238000011065 in-situ storage Methods 0.000 description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 4
- 239000012454 non-polar solvent Substances 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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- 125000001931 aliphatic group Chemical group 0.000 description 3
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
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- 150000002989 phenols Chemical class 0.000 description 3
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 3
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- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- HHJJPFYGIRKQOM-UHFFFAOYSA-N sodium;oxido-oxo-phenylphosphanium Chemical compound [Na+].[O-][P+](=O)C1=CC=CC=C1 HHJJPFYGIRKQOM-UHFFFAOYSA-N 0.000 description 3
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- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 2
- GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 description 2
- BVUXDWXKPROUDO-UHFFFAOYSA-N 2,6-di-tert-butyl-4-ethylphenol Chemical compound CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 BVUXDWXKPROUDO-UHFFFAOYSA-N 0.000 description 2
- RLYCRLGLCUXUPO-UHFFFAOYSA-N 2,6-diaminotoluene Chemical compound CC1=C(N)C=CC=C1N RLYCRLGLCUXUPO-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
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- DUICOUMZLQSAPN-UHFFFAOYSA-N 4,6-diethyl-5-methylbenzene-1,3-diamine Chemical compound CCC1=C(C)C(CC)=C(N)C=C1N DUICOUMZLQSAPN-UHFFFAOYSA-N 0.000 description 2
- IPDXWXPSCKSIII-UHFFFAOYSA-N 4-propan-2-ylbenzene-1,3-diamine Chemical compound CC(C)C1=CC=C(N)C=C1N IPDXWXPSCKSIII-UHFFFAOYSA-N 0.000 description 2
- CAHQGWAXKLQREW-UHFFFAOYSA-N Benzal chloride Chemical compound ClC(Cl)C1=CC=CC=C1 CAHQGWAXKLQREW-UHFFFAOYSA-N 0.000 description 2
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
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- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
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- 239000004813 Perfluoroalkoxy alkane Substances 0.000 description 2
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- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 125000002015 acyclic group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G73/101—Preparatory processes from tetracarboxylic acids or derivatives and diamines containing chain terminating or branching agents
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C—CHEMISTRY; METALLURGY
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/44—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling
- D04H1/46—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Textile Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP20120382118 EP2644640A1 (en) | 2012-03-30 | 2012-03-30 | Polyetherimides, methods of manufacture, and articles formed therefrom |
| EP12382118.3 | 2012-03-30 | ||
| PCT/US2013/034262 WO2013148944A1 (en) | 2012-03-30 | 2013-03-28 | Polyetherimides, methods of manufacture, and articles formed therefrom |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20140146160A true KR20140146160A (ko) | 2014-12-24 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020147030669A Abandoned KR20140146160A (ko) | 2012-03-30 | 2013-03-28 | 폴리에테르이미드, 이의 제조방법 및 이로부터 형성된 물품 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9181396B2 (enExample) |
| EP (2) | EP2644640A1 (enExample) |
| KR (1) | KR20140146160A (enExample) |
| CN (1) | CN104245795B (enExample) |
| ES (1) | ES2686344T3 (enExample) |
| IN (1) | IN2014DN07346A (enExample) |
| WO (1) | WO2013148944A1 (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9127127B2 (en) | 2012-10-03 | 2015-09-08 | Sabic Global Technologies B.V. | Polyetherimide compositions, methods of manufacture, and articles formed therefrom |
| US20140099510A1 (en) * | 2012-10-04 | 2014-04-10 | Hendrich Chiong | Methods of manufacture of bis(phthalimide)s and polyetherimides, and bis(phthalimide)s, and polyetherimides formed therefrom |
| US10377860B2 (en) * | 2013-09-13 | 2019-08-13 | Sabic Global Technologies B.V. | Polyetherimides, methods of manufacture, and articles formed therefrom |
| US10676571B2 (en) | 2013-12-02 | 2020-06-09 | Sabic Global Technologies B.V. | Polyetherimides with improved melt stability |
| US10822496B2 (en) | 2015-02-23 | 2020-11-03 | Sabic Global Technologies B.V. | Electrical tracking resistance compositions, articles formed therefrom, and methods of manufacture thereof |
| CN107250280A (zh) | 2015-02-23 | 2017-10-13 | 沙特基础工业全球技术有限公司 | 耐漏电起痕组合物、由其形成的制品及其制造方法 |
| US10647815B2 (en) | 2015-02-23 | 2020-05-12 | Sabic Global Technologies B.V. | Electrical tracking resistance compositions, articles formed therefrom, and methods of manufacture thereof |
| CN107406672B (zh) * | 2015-02-23 | 2020-01-10 | 沙特基础工业全球技术有限公司 | 耐漏电起痕组合物、由其形成的制品及其制造方法 |
| WO2016138388A1 (en) | 2015-02-27 | 2016-09-01 | Sabic Global Technologies B.V. | Process to make low color polyetherimide by halo-displacement and low color polyetherimide |
| CN107257817B (zh) * | 2015-02-27 | 2021-01-22 | 沙特基础工业全球技术有限公司 | 具有改善的颜色的聚醚酰亚胺及其制造方法 |
| WO2016187424A1 (en) * | 2015-05-19 | 2016-11-24 | Sabic Global Technologies B.V. | Polymeric compositions for implantable medical devices and header thereof |
| WO2016196268A1 (en) * | 2015-05-29 | 2016-12-08 | Sabic Global Technologies B.V. | Polyetherimide of improved color and process of preparing |
| WO2017017638A1 (en) * | 2015-07-29 | 2017-02-02 | Sabic Global Technologies B.V. | Polyetherimide composition for molding |
| EP3362502A1 (en) * | 2015-10-14 | 2018-08-22 | SABIC Global Technologies B.V. | Methods of manufacture of thermoplastic polymers |
| WO2017117343A1 (en) | 2015-12-31 | 2017-07-06 | Sabic Global Technologies B. V. | Polyetherimide compositions, methods of manufacture, and articles prepared therefrom |
| US10703920B2 (en) * | 2016-09-28 | 2020-07-07 | Ppg Industries Ohio, Inc. | Corrosion-resistant epoxidized vegetable oil can interior coating |
| US11292879B2 (en) | 2016-12-31 | 2022-04-05 | Shpp Global Technologies B.V. | Methods for the manufacture of polyetherimides and polyetherimides made by the method |
| CN109956875A (zh) * | 2017-12-22 | 2019-07-02 | 江苏国立化工科技有限公司 | 一种对苯二胺类橡胶防老剂及其制备方法 |
| CN108164452B (zh) * | 2018-02-09 | 2019-06-18 | 苏州科尔力化工有限公司 | 一种双(氯代邻苯二甲酰亚胺)的制备方法 |
| US11738921B2 (en) | 2018-03-23 | 2023-08-29 | Sumitomo Chemical Company, Limited | Banding band |
| CN111141848A (zh) * | 2020-01-03 | 2020-05-12 | 杭州瑞旭科技集团有限公司 | 一种永固紫的含量测定方法 |
| CN115044203A (zh) * | 2022-05-23 | 2022-09-13 | 中电科芜湖钻石飞机制造有限公司 | 低介电耐高温树脂基复合材料及其制备方法 |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3383092A (en) | 1963-09-06 | 1968-05-14 | Garrett Corp | Gas turbine with pulsating gas flows |
| US3671487A (en) | 1971-05-05 | 1972-06-20 | Gen Electric | Glass reinforced polyester resins containing polytetrafluoroethylene and flame retardant additives |
| US3723373A (en) | 1971-10-04 | 1973-03-27 | American Cyanamid Co | 0.1% to about 2.0% by weight polytetrafluoroethylene emulsion modified polyethylene terephthalate with improved processing characteristics |
| US4390665A (en) * | 1982-03-18 | 1983-06-28 | General Electric Company | Polyetherimide-EPDM terpolymer blends |
| US4417044A (en) | 1982-05-25 | 1983-11-22 | General Electric Company | Process for making polyetherimides |
| JPH0319838A (ja) * | 1989-06-17 | 1991-01-29 | Toshiba Chem Corp | 耐熱性積層板 |
| JPH0319837A (ja) * | 1989-06-17 | 1991-01-29 | Toshiba Chem Corp | 耐熱性積層板 |
| US5229482A (en) | 1991-02-28 | 1993-07-20 | General Electric Company | Phase transfer catalyzed preparation of aromatic polyether polymers |
| US5521230A (en) | 1992-11-17 | 1996-05-28 | General Electric Company | Method of dispersing solid additives in polymers and products made therewith |
| US6057403A (en) * | 1993-06-01 | 2000-05-02 | Spalding Sports Worldwide, Inc | Dual cores for golf balls |
| US5856421A (en) * | 1997-03-17 | 1999-01-05 | General Electric Company | Polyetherimide preparation method including addition of macrocyclic polyetherimide oligomers |
| US6270853B1 (en) * | 1997-06-20 | 2001-08-07 | Raytheon Company | Electrostatic powder coating of electrically non-conducting substrates |
| US6235866B1 (en) | 1999-10-06 | 2001-05-22 | General Electric Company | Slurry preparation of bis (halophthalimides) and of polyether polymers |
| US6700185B1 (en) * | 1999-11-10 | 2004-03-02 | Hitachi Chemical Co., Ltd. | Adhesive film for semiconductor, lead frame and semiconductor device using the same, and method for manufacturing semiconductor device |
| US6849706B1 (en) | 2003-08-25 | 2005-02-01 | General Electric Company | Copolyetherimides |
| US7714095B2 (en) * | 2003-08-25 | 2010-05-11 | Sabic Innovative Plastics Ip B.V. | Phase transfer catalyzed method for preparation of polyetherimides |
| US7125954B2 (en) * | 2005-01-27 | 2006-10-24 | General Electric Company | Method for producing polyether polymers |
| US7605222B2 (en) * | 2005-08-22 | 2009-10-20 | Sabic Innovative Plastics Ip B.V. | Copolyetherimides |
| US20070149629A1 (en) * | 2005-12-22 | 2007-06-28 | Michael Stephen Donovan | Expanded and expandable high glass transition temperature polymers |
| CN101528808A (zh) * | 2006-09-05 | 2009-09-09 | 沙伯基础创新塑料知识产权有限公司 | 聚醚聚合物的制备方法 |
| WO2008095071A1 (en) * | 2007-02-01 | 2008-08-07 | Invista Technologies S.Ar.L. | Polyester composition with improved gas barrier properties and articles thereof |
| US7999024B2 (en) * | 2007-06-22 | 2011-08-16 | Sabic Innovative Plastics Ip B.V. | Method of purifying a polymer |
| US8939438B2 (en) * | 2010-01-08 | 2015-01-27 | Lee Spring Company Llc | Plastic spring and method and apparatus for making the same |
-
2012
- 2012-03-30 EP EP20120382118 patent/EP2644640A1/en not_active Withdrawn
-
2013
- 2013-03-28 WO PCT/US2013/034262 patent/WO2013148944A1/en not_active Ceased
- 2013-03-28 ES ES13770078.7T patent/ES2686344T3/es active Active
- 2013-03-28 KR KR1020147030669A patent/KR20140146160A/ko not_active Abandoned
- 2013-03-28 US US13/851,981 patent/US9181396B2/en active Active
- 2013-03-28 CN CN201380016105.XA patent/CN104245795B/zh active Active
- 2013-03-28 EP EP13770078.7A patent/EP2831147B1/en active Active
-
2014
- 2014-09-02 IN IN7346DEN2014 patent/IN2014DN07346A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN104245795B (zh) | 2017-06-20 |
| ES2686344T3 (es) | 2018-10-17 |
| WO2013148944A1 (en) | 2013-10-03 |
| EP2831147B1 (en) | 2018-06-06 |
| EP2831147A4 (en) | 2015-11-25 |
| CN104245795A (zh) | 2014-12-24 |
| US9181396B2 (en) | 2015-11-10 |
| EP2644640A1 (en) | 2013-10-02 |
| US20130344313A1 (en) | 2013-12-26 |
| EP2831147A1 (en) | 2015-02-04 |
| IN2014DN07346A (enExample) | 2015-04-24 |
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