CN115073649A - 一种除氯剂及其制备方法和应用 - Google Patents
一种除氯剂及其制备方法和应用 Download PDFInfo
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- CN115073649A CN115073649A CN202210859287.8A CN202210859287A CN115073649A CN 115073649 A CN115073649 A CN 115073649A CN 202210859287 A CN202210859287 A CN 202210859287A CN 115073649 A CN115073649 A CN 115073649A
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- Prior art keywords
- chlorine
- agent
- epoxy resin
- reaction
- ketene
- 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.)
- Granted
Links
- 230000000382 dechlorinating effect Effects 0.000 title claims abstract description 25
- 238000002360 preparation method Methods 0.000 title abstract description 10
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 103
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 102
- 239000000460 chlorine Substances 0.000 claims abstract description 102
- 239000003822 epoxy resin Substances 0.000 claims abstract description 83
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 83
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 49
- 238000006243 chemical reaction Methods 0.000 claims abstract description 44
- 238000000034 method Methods 0.000 claims abstract description 28
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000007822 coupling agent Substances 0.000 claims abstract description 17
- 239000003999 initiator Substances 0.000 claims abstract description 16
- 239000003349 gelling agent Substances 0.000 claims abstract description 15
- 239000003960 organic solvent Substances 0.000 claims abstract description 12
- 238000006298 dechlorination reaction Methods 0.000 claims abstract description 10
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 10
- 230000001681 protective effect Effects 0.000 claims abstract description 6
- 239000011259 mixed solution Substances 0.000 claims abstract description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 39
- 239000012535 impurity Substances 0.000 claims description 36
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical group N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 24
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical group CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 claims description 18
- 239000000178 monomer Substances 0.000 claims description 17
- 239000002245 particle Substances 0.000 claims description 15
- 238000001914 filtration Methods 0.000 claims description 10
- 239000002516 radical scavenger Substances 0.000 claims description 10
- 229920002554 vinyl polymer Polymers 0.000 claims description 10
- 229960001413 acetanilide Drugs 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- KBGDCKHDBZJUKE-UHFFFAOYSA-N 1-(2,3,6-trimethylphenyl)-3-buten-2-one Chemical compound CC1=CC=C(C)C(CC(=O)C=C)=C1C KBGDCKHDBZJUKE-UHFFFAOYSA-N 0.000 claims description 8
- 230000035484 reaction time Effects 0.000 claims description 6
- 239000007789 gas Substances 0.000 claims description 5
- 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 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical group CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 claims description 4
- 239000000243 solution Substances 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 abstract description 46
- 238000000926 separation method Methods 0.000 abstract description 11
- 238000000199 molecular distillation Methods 0.000 abstract description 6
- 239000000463 material Substances 0.000 abstract description 4
- 230000003301 hydrolyzing effect Effects 0.000 abstract description 2
- 238000010438 heat treatment Methods 0.000 description 24
- 239000007787 solid Substances 0.000 description 14
- 238000003828 vacuum filtration Methods 0.000 description 12
- 238000001816 cooling Methods 0.000 description 7
- 239000000706 filtrate Substances 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 238000005303 weighing Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000004793 Polystyrene Substances 0.000 description 4
- 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 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000004611 spectroscopical analysis Methods 0.000 description 3
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 238000000967 suction filtration Methods 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- KUIZKZHDMPERHR-UHFFFAOYSA-N 1-phenylprop-2-en-1-one Chemical compound C=CC(=O)C1=CC=CC=C1 KUIZKZHDMPERHR-UHFFFAOYSA-N 0.000 description 1
- LRWZZZWJMFNZIK-UHFFFAOYSA-N 2-chloro-3-methyloxirane Chemical compound CC1OC1Cl LRWZZZWJMFNZIK-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004100 electronic packaging Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/08—Styrene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F216/36—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by a ketonic radical
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/04—Polymerisation in solution
- C08F2/06—Organic solvent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F230/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
- C08F230/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal
- C08F230/08—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
- C08F230/085—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon the monomer being a polymerisable silane, e.g. (meth)acryloyloxy trialkoxy silanes or vinyl trialkoxysilanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/26—Removing halogen atoms or halogen-containing groups from the molecule
-
- 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
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/025—Polycondensates containing more than one epoxy group per molecule characterised by the purification methods used
-
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
- C08K5/23—Azo-compounds
- C08K5/235—Diazo and polyazo compounds
-
- 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
- C08K5/54—Silicon-containing compounds
- C08K5/541—Silicon-containing compounds containing oxygen
- C08K5/5425—Silicon-containing compounds containing oxygen containing at least one C=C bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2810/00—Chemical modification of a polymer
- C08F2810/40—Chemical modification of a polymer taking place solely at one end or both ends of the polymer backbone, i.e. not in the side or lateral chains
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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)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Epoxy Resins (AREA)
Abstract
Description
实施例 | 除杂前环氧树脂氯含量/ppm | 除杂后环氧树脂氯含量/ppm |
1 | 1222 | 486 |
2 | 1214 | 459 |
3 | 1216 | 437 |
4 | 1207 | 425 |
5 | 1244 | 463 |
6 | 1203 | 431 |
Claims (10)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210859287.8A CN115073649B (zh) | 2022-07-20 | 2022-07-20 | 一种除氯剂及其制备方法和应用 |
US18/174,618 US20240026047A1 (en) | 2022-07-20 | 2023-02-25 | Antichlor And Preparation Method As Well As Application Thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202210859287.8A CN115073649B (zh) | 2022-07-20 | 2022-07-20 | 一种除氯剂及其制备方法和应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN115073649A true CN115073649A (zh) | 2022-09-20 |
CN115073649B CN115073649B (zh) | 2023-10-27 |
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CN202210859287.8A Active CN115073649B (zh) | 2022-07-20 | 2022-07-20 | 一种除氯剂及其制备方法和应用 |
Country Status (2)
Country | Link |
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US (1) | US20240026047A1 (zh) |
CN (1) | CN115073649B (zh) |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61252222A (ja) * | 1985-05-01 | 1986-11-10 | Asahi Chiba Kk | エポキシ樹脂中の塩素の除去方法 |
JPS61252221A (ja) * | 1985-05-01 | 1986-11-10 | Asahi Chiba Kk | エポキシ樹脂の精製方法 |
JPS6264817A (ja) * | 1985-09-17 | 1987-03-23 | Yuka Shell Epoxy Kk | エポキシ樹脂の精製方法 |
JPS62235314A (ja) * | 1986-04-05 | 1987-10-15 | Toto Kasei Kk | エポキシ樹脂の精製方法 |
JPH01108218A (ja) * | 1987-10-21 | 1989-04-25 | Mitsui Petrochem Ind Ltd | エポキシ樹脂の精製方法 |
JPH01108217A (ja) * | 1987-10-21 | 1989-04-25 | Mitsui Petrochem Ind Ltd | エポキシ樹脂の精製方法 |
JPH01108219A (ja) * | 1987-10-21 | 1989-04-25 | Mitsui Petrochem Ind Ltd | エポキシ樹脂の精製方法 |
JPH1036484A (ja) * | 1996-07-26 | 1998-02-10 | Dainippon Ink & Chem Inc | エポキシ樹脂の精製方法 |
JPH11106472A (ja) * | 1997-10-06 | 1999-04-20 | Nippon Kayaku Co Ltd | エポキシ樹脂の製造法 |
JP2002308963A (ja) * | 2001-04-11 | 2002-10-23 | Nippon Kayaku Co Ltd | エポキシ樹脂の製造方法 |
JP2004211028A (ja) * | 2003-01-08 | 2004-07-29 | Toto Kasei Co Ltd | エポキシ樹脂の精製方法及び半導体封止用エポキシ樹脂組成物 |
JP2013095916A (ja) * | 2011-11-07 | 2013-05-20 | Asahi Kasei E-Materials Corp | エポキシ樹脂の製造方法及び該製造方法を用いて得られたエポキシ樹脂 |
JP2013100384A (ja) * | 2011-11-07 | 2013-05-23 | Asahi Kasei E-Materials Corp | エポキシ樹脂の製造方法及び該製造方法を用いて得られたエポキシ樹脂 |
-
2022
- 2022-07-20 CN CN202210859287.8A patent/CN115073649B/zh active Active
-
2023
- 2023-02-25 US US18/174,618 patent/US20240026047A1/en active Pending
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61252222A (ja) * | 1985-05-01 | 1986-11-10 | Asahi Chiba Kk | エポキシ樹脂中の塩素の除去方法 |
JPS61252221A (ja) * | 1985-05-01 | 1986-11-10 | Asahi Chiba Kk | エポキシ樹脂の精製方法 |
JPS6264817A (ja) * | 1985-09-17 | 1987-03-23 | Yuka Shell Epoxy Kk | エポキシ樹脂の精製方法 |
JPS62235314A (ja) * | 1986-04-05 | 1987-10-15 | Toto Kasei Kk | エポキシ樹脂の精製方法 |
JPH01108218A (ja) * | 1987-10-21 | 1989-04-25 | Mitsui Petrochem Ind Ltd | エポキシ樹脂の精製方法 |
JPH01108217A (ja) * | 1987-10-21 | 1989-04-25 | Mitsui Petrochem Ind Ltd | エポキシ樹脂の精製方法 |
JPH01108219A (ja) * | 1987-10-21 | 1989-04-25 | Mitsui Petrochem Ind Ltd | エポキシ樹脂の精製方法 |
JPH1036484A (ja) * | 1996-07-26 | 1998-02-10 | Dainippon Ink & Chem Inc | エポキシ樹脂の精製方法 |
JPH11106472A (ja) * | 1997-10-06 | 1999-04-20 | Nippon Kayaku Co Ltd | エポキシ樹脂の製造法 |
JP2002308963A (ja) * | 2001-04-11 | 2002-10-23 | Nippon Kayaku Co Ltd | エポキシ樹脂の製造方法 |
JP2004211028A (ja) * | 2003-01-08 | 2004-07-29 | Toto Kasei Co Ltd | エポキシ樹脂の精製方法及び半導体封止用エポキシ樹脂組成物 |
JP2013095916A (ja) * | 2011-11-07 | 2013-05-20 | Asahi Kasei E-Materials Corp | エポキシ樹脂の製造方法及び該製造方法を用いて得られたエポキシ樹脂 |
JP2013100384A (ja) * | 2011-11-07 | 2013-05-23 | Asahi Kasei E-Materials Corp | エポキシ樹脂の製造方法及び該製造方法を用いて得られたエポキシ樹脂 |
Non-Patent Citations (1)
Title |
---|
张军营;李建华;李婧婧;萧华;: "高纯和低可水解氯含量环氧树脂的制备", 石油化工, no. 11, pages 1091 - 1094 * |
Also Published As
Publication number | Publication date |
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US20240026047A1 (en) | 2024-01-25 |
CN115073649B (zh) | 2023-10-27 |
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