JP5074551B2 - リン系エポキシ樹脂半固化物およびその製造方法 - Google Patents
リン系エポキシ樹脂半固化物およびその製造方法 Download PDFInfo
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- JP5074551B2 JP5074551B2 JP2010103369A JP2010103369A JP5074551B2 JP 5074551 B2 JP5074551 B2 JP 5074551B2 JP 2010103369 A JP2010103369 A JP 2010103369A JP 2010103369 A JP2010103369 A JP 2010103369A JP 5074551 B2 JP5074551 B2 JP 5074551B2
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- 239000003822 epoxy resin Substances 0.000 title claims description 49
- 229920000647 polyepoxide Polymers 0.000 title claims description 49
- 238000004519 manufacturing process Methods 0.000 title claims description 21
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 title claims description 6
- 239000000463 material Substances 0.000 title description 6
- 229910052698 phosphorus Inorganic materials 0.000 claims description 59
- 239000011574 phosphorus Substances 0.000 claims description 59
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 50
- 239000000126 substance Substances 0.000 claims description 42
- 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 22
- 229930185605 Bisphenol Natural products 0.000 claims description 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
- 238000006243 chemical reaction Methods 0.000 claims description 14
- -1 imidazole compound Chemical class 0.000 claims description 14
- 239000003054 catalyst Substances 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 8
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 8
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 7
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical group C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims description 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 5
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical group C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
- HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 claims description 4
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 claims description 4
- 150000004714 phosphonium salts Chemical group 0.000 claims description 4
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 4
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 4
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 claims description 4
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 claims description 3
- ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 claims description 2
- 229910015900 BF3 Inorganic materials 0.000 claims description 2
- KXHPPCXNWTUNSB-UHFFFAOYSA-M benzyl(trimethyl)azanium;chloride Chemical group [Cl-].C[N+](C)(C)CC1=CC=CC=C1 KXHPPCXNWTUNSB-UHFFFAOYSA-M 0.000 claims description 2
- 125000003700 epoxy group Chemical group 0.000 claims description 2
- HZZUMXSLPJFMCB-UHFFFAOYSA-M ethyl(triphenyl)phosphanium;acetate Chemical group CC([O-])=O.C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 HZZUMXSLPJFMCB-UHFFFAOYSA-M 0.000 claims description 2
- 150000002642 lithium compounds Chemical class 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- 239000000047 product Substances 0.000 description 30
- 230000000052 comparative effect Effects 0.000 description 24
- 238000012360 testing method Methods 0.000 description 19
- 239000004593 Epoxy Substances 0.000 description 14
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical group CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 11
- 238000010586 diagram Methods 0.000 description 11
- 239000007788 liquid Substances 0.000 description 11
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 11
- 239000003513 alkali Substances 0.000 description 9
- BSYJHYLAMMJNRC-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-ol Chemical compound CC(C)(C)CC(C)(C)O BSYJHYLAMMJNRC-UHFFFAOYSA-N 0.000 description 8
- 230000009477 glass transition Effects 0.000 description 8
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 7
- 238000002485 combustion reaction Methods 0.000 description 7
- 239000003063 flame retardant Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 238000004090 dissolution Methods 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 6
- BJHJDRPKLAKFSU-UHFFFAOYSA-N C1(=CC=CC=C1)O.C1(=CC=CC=C1)O.[P] Chemical compound C1(=CC=CC=C1)O.C1(=CC=CC=C1)O.[P] BJHJDRPKLAKFSU-UHFFFAOYSA-N 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000003377 acid catalyst Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000007711 solidification Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- NMMHFJLCXJKUEG-UHFFFAOYSA-N biphenylene;phosphoric acid Chemical group OP(O)(O)=O.C1=CC=C2C3=CC=CC=C3C2=C1 NMMHFJLCXJKUEG-UHFFFAOYSA-N 0.000 description 3
- 150000003017 phosphorus Chemical class 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 238000005979 thermal decomposition reaction Methods 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- NPFYZDNDJHZQKY-UHFFFAOYSA-N 4-Hydroxybenzophenone Chemical compound C1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 NPFYZDNDJHZQKY-UHFFFAOYSA-N 0.000 description 2
- 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 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000006735 epoxidation reaction Methods 0.000 description 2
- 238000010265 fast atom bombardment Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- WHQSYGRFZMUQGQ-UHFFFAOYSA-N n,n-dimethylformamide;hydrate Chemical compound O.CN(C)C=O WHQSYGRFZMUQGQ-UHFFFAOYSA-N 0.000 description 2
- 150000002903 organophosphorus compounds Chemical class 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- STJANKPTIVPGNU-UHFFFAOYSA-N (4-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=C(C(=O)C2=CC=CC=C2)C=C1.OC1=CC=C(C(=O)C2=CC=CC=C2)C=C1 STJANKPTIVPGNU-UHFFFAOYSA-N 0.000 description 1
- AAOADXIHXYIOMT-UHFFFAOYSA-N 1,1'-biphenyl;phosphoric acid Chemical compound OP(O)(O)=O.C1=CC=CC=C1C1=CC=CC=C1 AAOADXIHXYIOMT-UHFFFAOYSA-N 0.000 description 1
- MVNVIVWSAFEIII-UHFFFAOYSA-N 1-(4-hydroxyphenyl)ethanone Chemical compound CC(=O)C1=CC=C(O)C=C1.CC(=O)C1=CC=C(O)C=C1 MVNVIVWSAFEIII-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 description 1
- TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 102000006335 Phosphate-Binding Proteins Human genes 0.000 description 1
- 108010058514 Phosphate-Binding Proteins Proteins 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000004841 bisphenol A epoxy resin Substances 0.000 description 1
- 239000004842 bisphenol F epoxy resin Substances 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- 229910052811 halogen oxide Inorganic materials 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/30—Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen
- C08G59/304—Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen and nitrogen containing phosphorus
-
- C—CHEMISTRY; METALLURGY
- 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
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/14—Polycondensates modified by chemical after-treatment
- C08G59/1433—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
- C08G59/1488—Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing phosphorus
Description
本発明の実施例においては、リン系ビスフェノールの製造方法を開示するものであって、化学式(a)で表される有機環状リン化合物、化学式(b)で表される化合物、化学式(c)で表される、フェノールおよび酸触媒で反応を行い、リン系ビスフェノールを生成することを含む。
有機環状リン化合物DOPO(9,10−ジヒドロ−9−オキサ−10−ホスファフェナントレン10−オキシド)を10.81g(0.05モル)、フェノールを23.5g(0.25モル)、4’−ヒドロキシアセトフェノンを6.81g(0.05モル)、p−トルエンスルホン酸を0.432g(DOPO使用量の4wt%)計量して、250mlの三口フラスコに投入した。続いて、反応温度を130℃にまで上昇させて、24時間反応を維持した後、撹拌を止めた。フラスコを室温にまで冷却した。このとき、自然に析出した部分をエタノールで洗浄した後、濾過・乾燥させて、白色粉末であるリン系ビスフェノールを得た。その構造は下記化学式に表されるとおりである。
有機環状リン化合物DOPO(9,10−ジヒドロ−9−オキサ−10−ホスファフェナントレン10−オキシド)を10.81g(0.05モル)、フェノールを23.5g(0.25モル)、4−ヒドロキシベンゾフェノンを9.91g(0.05モル)、p−トルエンスルホン酸を0.216g(DOPO使用量の2wt%)計量して、250mlの三口フラスコに投入した。続いて、反応温度を130°Cにまで上昇させて、24時間反応を維持した後、撹拌を止めた。フラスコを室温にまで冷却して、エタノールで溶解させた後、熱水中に投入して析出を行った。析出物を濾過・乾燥して、融点が288°Cである下記式で表されるリン系ビスフェノールを収率87%で得た。
次に、リン系エポキシ樹脂半固化物の製造方法では、化学式(I)で表されるリン系ビスフェノール、化学式(II)で表されるエポキシ化物および触媒を含む系で鎖延長反応を行い、化学式(I)で表されるリン系エポキシ樹脂半固化物を生成した。
前記実施例1のリン含有ビスフェノール単量体および比較例1に対して耐アルカリ性試験を行った。比較例1の構造は前記化学式(I)であり、Rは水素である(構造を以下に示す)。
Claims (10)
- 化学式(I)で表される構造を備えたことを特徴とするリン系エポキシ樹脂半固化物。
- 化学式(I)のリン系ビスフェノールと、
(式中、当該Rはメチル基またはフェニル基であり、Yは下記の基からなる群から選ばれ、
- 前記鎖延長反応が100℃〜200℃で行われることを特徴とする請求項2に記載の製造方法。
- 化学式(II)のエポキシ樹脂のエポキシ基の当量数と化学式(I)のリン系ビスフェノールのフェノール基の当量数との比が1:1〜10:1であることを特徴とする請求項2に記載の製造方法。
- 前記触媒の使用量が、化学式(II)のエポキシ樹脂の使用量に対し0.1wt%〜5wt%であることを特徴とする請求項2に記載の製造方法。
- 前記触媒がイミダゾール化合物、第3級ホスフィン、第3級アミン、第4級ホスホニウム塩、三フッ化ホウ素錯塩、リチウム化合物または第4級アンモニウム塩を含むことを特徴とする請求項2に記載の製造方法。
- 前記イミダゾール化合物が2−フェニルイミダゾールまたは2−メチルイミダゾールであることを特徴とする請求項6に記載の製造方法。
- 前記第3級ホスフィンがトリフェニルホスファンであることを特徴とする請求項6に記載の製造方法。
- 前記第4級アンモニウム塩が塩化ベンジルトリメチルアンモニウム、塩化ベンジルトリエチルアンモニウムまたは塩化テトラブチルアンモニウムであることを特徴とする請求項6に記載の製造方法。
- 前記第4級ホスホニウム塩がエチルトリフェニルホスホニウムアセテートまたはエチルトリフェニルホスホニウムハロゲン化合物であることを特徴とする請求項6に記載の製造方法。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW099100837A TWI382035B (zh) | 2010-01-13 | 2010-01-13 | 磷系環氧樹脂半固化物及其製備方法 |
TW099100837 | 2010-01-13 |
Publications (2)
Publication Number | Publication Date |
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JP2011144345A JP2011144345A (ja) | 2011-07-28 |
JP5074551B2 true JP5074551B2 (ja) | 2012-11-14 |
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JP2010103369A Active JP5074551B2 (ja) | 2010-01-13 | 2010-04-28 | リン系エポキシ樹脂半固化物およびその製造方法 |
Country Status (3)
Country | Link |
---|---|
US (1) | US8426547B2 (ja) |
JP (1) | JP5074551B2 (ja) |
TW (1) | TWI382035B (ja) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
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TWI388567B (zh) * | 2008-11-14 | 2013-03-11 | Chang Chun Plastics Co Ltd | 含磷化合物及其製法 |
WO2012039473A1 (ja) * | 2010-09-22 | 2012-03-29 | 宇部興産株式会社 | 有機リン化合物及びその製造方法 |
CN103965245B (zh) * | 2013-01-28 | 2016-06-08 | 中国科学院宁波材料技术与工程研究所 | 一种含磷生物基二酸二缩水甘油酯及其制备方法和应用 |
CN105061711B (zh) * | 2015-07-25 | 2017-09-01 | 福建师范大学泉港石化研究院 | 一种端基为环氧基的dopo型反应型阻燃剂及其制备方法和应用 |
US9546262B1 (en) | 2015-11-04 | 2017-01-17 | Chang Chun Plastics Co. Ltd. | Phosphorous containing compounds and process for synthesis |
JP6733198B2 (ja) | 2016-02-09 | 2020-07-29 | セイコーエプソン株式会社 | インクジェットインク、インクカートリッジおよびインクジェット記録方法 |
JP7098719B2 (ja) | 2018-03-30 | 2022-07-11 | 富士フイルム株式会社 | 前処理液、インクセット、画像記録物、画像記録用基材、画像記録用基材の製造方法及び画像記録方法 |
CN109354673B (zh) * | 2018-10-15 | 2020-07-31 | 福建师范大学 | 一种基于硅噻唑dopo型阻燃剂改性的环氧树脂制备方法 |
US10899871B2 (en) | 2019-04-23 | 2021-01-26 | Chang Chun Plastics Co., Ltd. | Phosphorous containing epoxy resins and process for synthesis |
US10961208B1 (en) | 2019-12-24 | 2021-03-30 | Chang Chun Plastics Co., Ltd. | Product of glycidyl ether of a mono or polyhydric phenol |
CN111057217B (zh) * | 2019-12-26 | 2021-08-27 | 广东生益科技股份有限公司 | 一种热固性环氧树脂组合物及使用其的半固化片、层压板和印制线路板 |
CN116284748A (zh) * | 2023-02-02 | 2023-06-23 | 四川东材科技集团股份有限公司 | 一种高阻燃大分子含磷固体苯氧树脂及其制备方法 |
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