CN102887981A - Preparation method of PTFEMA (trifluoroethyl methacrylate)-b-PSt fluorine-containing block copolymer - Google Patents

Preparation method of PTFEMA (trifluoroethyl methacrylate)-b-PSt fluorine-containing block copolymer Download PDF

Info

Publication number
CN102887981A
CN102887981A CN2011102067375A CN201110206737A CN102887981A CN 102887981 A CN102887981 A CN 102887981A CN 2011102067375 A CN2011102067375 A CN 2011102067375A CN 201110206737 A CN201110206737 A CN 201110206737A CN 102887981 A CN102887981 A CN 102887981A
Authority
CN
China
Prior art keywords
ptfema
pst
block copolymer
evocating agent
macromole evocating
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.)
Pending
Application number
CN2011102067375A
Other languages
Chinese (zh)
Inventor
侯丽华
黄维
张广维
彭波
解令海
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.)
WUXI FOUNTAIN TECH Co Ltd
Original Assignee
WUXI FOUNTAIN TECH Co Ltd
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.)
Filing date
Publication date
Application filed by WUXI FOUNTAIN TECH Co Ltd filed Critical WUXI FOUNTAIN TECH Co Ltd
Priority to CN2011102067375A priority Critical patent/CN102887981A/en
Publication of CN102887981A publication Critical patent/CN102887981A/en
Pending legal-status Critical Current

Links

Images

Landscapes

  • Graft Or Block Polymers (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

The invention provides a preparation method of a PTFEMA (trifluoroethyl methacrylate)-b-PSt fluorine-containing block copolymer. A macroinitiator takes ethyl-2-bromopropionate as an initiator, cuprous chloride/bipyridine as a catalysis system and PTFEMA as a monomer, and a PTFEMA-Br macroinitiator of which the end group contains an alpha-bromine atom is synthesized by an ATRP (atom transfer radical polymerization) method; and the macroinitiator initiates the styrene (St) polymerization to obtain a PTFEMA-b-PSt fluorine-containing block copolymer with relatively narrow molecular weight distribution.

Description

A kind of preparation method of PTFEMA-b-PSt fluorinated block copolymer
Technical field
The present invention relates to atom transfer radical polymerization (ATRP) method, be specially a kind of preparation method of PTFEMA-b-PSt fluorinated block copolymer.
Background technology
Nineteen ninety-five, the reported first such as doctor Wang Jinshan of U.S. Carnegie Mellon University, K.Maty jaszewski transition metal-catalyzed controllable free-radical polymerisation, be referred to as atom transfer radical polymerization (Atom Transfer Radical Polymerization, ATRP).
In recent years, along with the development of science and technology, the macromolecular material that preparation has specified structure and molecular weight has become the focus that people study, i.e. polymer design.By polymer design, can obtain the polymer materials of expected structure and performance, for scientific research and suitability for industrialized production provide wide development space.In the specific implementation method of various polymer designs, the ATRP technology is the comparatively ripe experimental technique of using, and is bringing into play in actual applications more and more important effect.
Compare with other polymer design means, ATRP technically with industry on sharpest edges be: practical monomer is extensive, reaction conditions is gentle, monomer, solvent, agent treated are simple, polymerization technique equipment simple (equipment of general radical polymerization gets final product), polymerization process is various, can adopt body, solution, suspension, emulsion polymerization, even also can polymerization in supercritical co.Along with the variation of the high efficiency of catalyst system, spike, polyreaction low temperature, technique simplification etc., make ATRP that very tempting industrial prospect be arranged.
Carbon-fluorine bond in the fluoropolymer (C-F)Bond energy than hydrocarbon key (C-H)Bond energy large; can play a protective role to high polymer main chain; so that fluoropolymer has good " three high two hate " property; be high-weatherability, high heat resistance, high stability and hydrophobic, hate oil characteristic; in modern industry, bring into play very important effect, be widely used in numerous industries and the fields such as defence and military, the top science, boats and ships, machinery, chemical industry, electronics, electrical equipment, semi-conductor, medical science (artificial organ), building.
In the preparation method of traditional fluoropolymer, a class is synthetic for the Fluorine containing olefine take PTFE, PVDF etc. as representative, mainly adopts suspension polymerization and emulsion polymerization, and the product property that obtains is excellent, but has the relatively poor problem of processed-type; Another kind of is to carry out copolymerization with various of monomer and fluorochemical monomer, the difficult control of the product structure that obtains and molecular weight, thereby be difficult to bring into play to greatest extent the premium properties of fluoropolymer, in such cases, just demonstrate its unique advantage with the synthetic fluorinated copolymer of ATRP method, this polymerization process is mainly used in the synthetic of segmented copolymer and graft copolymer.
Summary of the invention
The invention provides a kind of preparation method of PTFEMA-b-PSt fluorinated block copolymer, wherein macromole evocating agent is as initiator take ethyl-alpha-bromopropionate, take cuprous chloride/bipyridine as catalyst system, trifluoroethyl methacrylate (PTFEMA) is monomer, contains polymethyl acrylic acid trifluoro ethyl ester (PTFEMA-Br) macromole evocating agent of a α-bromine atoms by the synthetic end group of ATRP method; Cause vinylbenzene (St) polymerization with this macromole evocating agent, obtained the narrower PTFEMA-b-PSt fluorinated block copolymer of molecular weight distribution.
The present invention's realization by following technical solution:
A, a kind of end group are polymethyl acrylic acid fluorine ethyl ester (PTFEMA-Br) macromole evocating agent of α-bromine atoms, and its chemical structural formula is as shown in the formula shown in the I:
Figure 2011102067375100002DEST_PATH_IMAGE001
The formula I
N is the natural number of 20-100;
Described PTFEMA-Br macromole evocating agent is to be prepared from by the ATRP polymerization process, and concrete operation step is as follows:
(1) processing of trifluoroethyl methacrylate: with deionized water the trifluoroethyl methacrylate monomer is washed till neutrality, then uses successively CaCl 2And CaH 2Soaked respectively 2 days, at last under nitrogen protection and at CaH 2There is lower underpressure distillation purifying, preserves in 0-4 ℃ of sealing, for subsequent use;
(2) prepare the PTFEMA-Br macromole evocating agent by the ATRP polymerization process: trifluoroethyl methacrylate monomer, 2.0-20 mass parts ethyl-alpha-bromopropionate initiator, 0.2-20 mass parts bipyridine and 300-550 mass parts organic solvent that 100 mass parts steps (1) are handled well mix, it is freezing that cryosel is bathed, and vacuumizes, drum nitrogen 3-5 time to be to remove oxygen; Then under nitrogen protection, be warming up to 60-120 ℃, add 0.2-30 mass parts cuprous chloride reaction 1-10h, obtain PTFEMA-Br macromole evocating agent solution;
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-Br macromole evocating agent to constant weight;
Described organic solvent comprises toluene, Isosorbide-5-Nitrae-dioxane and butanone etc.;
It is as follows that described cryosel is bathed freezing condition: add 20 gram CaCl in 100 gram trash ices 26H 2O stirs and obtains.
B, with PTFEMA-Br as the synthetic PTFEMA-b-PSt segmented copolymer of ATRP macromole evocating agent:
Described PTFEMA-Br ATRP macromole evocating agent is applied to the ATRP polyreaction and prepares the narrower PTFEMA-b-PSt fluorinated block copolymer of molecular weight distribution, and it may further comprise the steps:
(1) the 5%NaOH aqueous solution and deionized water wash are used respectively in cinnamic processing, and be for subsequent use behind the underpressure distillation purifying behind the anhydrous magnesium sulfate drying;
(2) 100 mass parts styrene monomers, 1-200 mass parts PTFEMA-Br ATRP macromole evocating agent and 0.01-20 mass parts bipyridine and 400-600 mass parts organic solvent are mixed, it is freezing that cryosel is bathed, and vacuumizes, drum nitrogen 3-5 time to be to remove oxygen; Then under nitrogen protection, be warming up to 90-120 ℃, add 0.01-30 mass parts cuprous chloride reaction 2-30h, obtain the PTFEMA-b-PSt fluorinated block copolymer;
Figure 245561DEST_PATH_IMAGE002
Figure 333734DEST_PATH_IMAGE002
Figure 39521DEST_PATH_IMAGE002
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-b-PSt fluorinated block copolymer to constant weight;
Described organic solvent comprises Isosorbide-5-Nitrae-dioxane and butanone;
It is as follows that described cryosel is bathed freezing condition: add 20 gram CaCl in 100 gram trash ices 26H 2O stirs and obtains.
The present invention has at first prepared PTFEMA-Br by the ATRP polymerization process, then causes styrene polymerization with this as the ATRP macromole evocating agent, obtains the PTFEMA-b-PSt fluorinated block copolymer.The different PTFEMA-Br macromole evocating agent of molecular weight causes vinylbenzene and carries out the ATRP polymerization, obtains different chain lengths, and the fluorinated block copolymer of different structure has realized that preparation has the macromolecular material of specified structure and molecular size.
Description of drawings
Fig. 1 is the reaction scheme figure of synthetic PTFEMA-Br macromole evocating agent;
Fig. 2 is the synthetic route chart of synthetic PTFEMA-b-PSt segmented copolymer.
Embodiment
The invention will be further described below in conjunction with Fig. 1 and Fig. 2:
Embodiment 1
Polymethyl acrylic acid trifluoro ethyl ester (PTFEMA-Br) macromole evocating agent of a, a kind of α-bromine atoms, its chemical structural formula is as shown in the formula shown in the I, and described PTFEMA-Br macromole evocating agent is to be prepared from by the ATRP polymerization process, and concrete operation step is as follows:
(1) processing of trifluoroethyl methacrylate: with deionized water the trifluoroethyl methacrylate monomer is washed till neutrality, then uses successively CaCl 2And CaH 2Soaked respectively 2 days, at last under nitrogen protection and at CaH 2There is lower underpressure distillation purifying, preserves in 0-4 ℃ of sealing, for subsequent use;
(2) prepare the PTFEMA-Br macromole evocating agent by the ATRP polymerization process: trifluoroethyl methacrylate monomer, 2g ethyl-alpha-bromopropionate initiator, 0.2g bipyridine and 300g toluene that 100g step (1) is handled well mix, and add 20 gram CaCl in 100 gram trash ices 26H 2The stir cryosel that obtains of O is bathed freezingly, vacuumizes, drum nitrogen 3 times is with except oxygen; Then under nitrogen protection, be warming up to 120 ℃, add 30g cuprous chloride reaction 1h, obtain PTFEMA-Br macromole evocating agent solution, record number-average molecular weight Mn=4.50 * 10 by gel permeation chromatography (GPC) method 3, polydispersity coefficient PDI=1.22.Determine this macromole evocating agent structural formula I n=20 according to infrared spectra, NMR (Nuclear Magnetic Resonance) spectrum, GPC data and reaction principle;
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-Br macromole evocating agent to constant weight;
B, with PTFEMA-Br as the synthetic PTFEMA-b-PSt segmented copolymer of ATRP macromole evocating agent:
Described PTFEMA-Br ATRP macromole evocating agent is applied to the ATRP polyreaction and prepares the narrower PTFEMA-b-PSt fluorinated block copolymer of molecular weight distribution, and it may further comprise the steps:
(1) the 5%NaOH aqueous solution and deionized water wash are used respectively in cinnamic processing, and be for subsequent use behind the underpressure distillation purifying behind the anhydrous magnesium sulfate drying;
(2) with 100g styrene monomer, 1gPTFEMA-Br ATRP macromole evocating agent and 0.01g bipyridine and 400g1, the 4-dioxane mixes, and adds 20 gram CaCl in 100 gram trash ices 26H 2The stir cryosel that obtains of O is bathed freezingly, vacuumizes, drum nitrogen 3 times to be to remove oxygen; Then under nitrogen protection, be warming up to 90 ℃, add 0.01g cuprous chloride reaction 30h, obtain the PTFEMA-b-PSt fluorinated block copolymer; Record number-average molecular weight Mn=1.32 * 10 by gel permeation chromatography (GPC) method 4, polydispersity coefficient PDI=1.24;
Figure 686272DEST_PATH_IMAGE002
Figure 415194DEST_PATH_IMAGE002
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-b-PSt fluorinated block copolymer to constant weight.
Embodiment 2
Polymethyl acrylic acid trifluoro ethyl ester (PTFEMA-Br) macromole evocating agent of a, a kind of α-bromine atoms, its chemical structural formula is as shown in the formula shown in the I, and described PTFEMA-Br macromole evocating agent is to be prepared from by the ATRP polymerization process, and concrete operation step is as follows:
(1) processing of trifluoroethyl methacrylate: with deionized water the trifluoroethyl methacrylate monomer is washed till neutrality, then uses successively CaCl 2And CaH 2Soaked respectively 2 days, at last under nitrogen protection and at CaH 2There is lower underpressure distillation purifying, preserves in 0-4 ℃ of sealing, for subsequent use;
(2) prepare the PTFEMA-Br macromole evocating agent by the ATRP polymerization process: trifluoroethyl methacrylate monomer, 8g ethyl-alpha-bromopropionate initiator, 7g bipyridine and 400g1 that 100g step (1) is handled well, the 4-dioxane mixes, and adds 20 gram CaCl in 100 gram trash ices 26H 2The stir cryosel that obtains of O is bathed freezingly, vacuumizes, drum nitrogen 4 times is with except oxygen; Then under nitrogen protection, be warming up to 100 ℃, add 20g cuprous chloride reaction 7h, obtain PTFEMA-Br macromole evocating agent solution, record number-average molecular weight Mn=7.83 * 10 by gel permeation chromatography (GPC) method 3, polydispersity coefficient PDI=1.23.Determine this macromole evocating agent structural formula I n=45 according to infrared spectra, NMR (Nuclear Magnetic Resonance) spectrum, GPC data and reaction principle;
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-Br macromole evocating agent to constant weight;
B, with PTFEMA-Br as the synthetic PTFEMA-b-PSt segmented copolymer of ATRP macromole evocating agent:
Described PTFEMA-Br ATRP macromole evocating agent is applied to the ATRP polyreaction and prepares the narrower PTFEMA-b-PSt fluorinated block copolymer of molecular weight distribution, and it may further comprise the steps:
(1) the 5%NaOH aqueous solution and deionized water wash are used respectively in cinnamic processing, and be for subsequent use behind the underpressure distillation purifying behind the anhydrous magnesium sulfate drying;
(2) with 100g styrene monomer, 70gPTFEMA-Br ATRP macromole evocating agent and 7g bipyridine and 470g1, the 4-dioxane mixes, and adds 20 gram CaCl in 100 gram trash ices 26H 2The stir cryosel that obtains of O is bathed freezingly, vacuumizes, drum nitrogen 4 times to be to remove oxygen; Then under nitrogen protection, be warming up to 100 ℃, add 10g cuprous chloride reaction 21h, obtain the PTFEMA-b-PSt fluorinated block copolymer; Record number-average molecular weight Mn=2.42 * 10 by gel permeation chromatography (GPC) method 4, polydispersity coefficient PDI=1.24;
Figure 867352DEST_PATH_IMAGE002
Figure 638999DEST_PATH_IMAGE002
Figure 651954DEST_PATH_IMAGE002
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-b-PSt fluorinated block copolymer to constant weight.
Embodiment 3
Polymethyl acrylic acid trifluoro ethyl ester (PTFEMA-Br) macromole evocating agent of a, a kind of α-bromine atoms, its chemical structural formula is as shown in the formula shown in the I, and described PTFEMA-Br macromole evocating agent is to be prepared from by the ATRP polymerization process, and concrete operation step is as follows:
(1) processing of trifluoroethyl methacrylate: with deionized water the trifluoroethyl methacrylate monomer is washed till neutrality, then uses successively CaCl 2And CaH 2Soaked respectively 2 days, at last under nitrogen protection and at CaH 2There is lower underpressure distillation purifying, preserves in 0-4 ℃ of sealing, for subsequent use;
(2) prepare the PTFEMA-Br macromole evocating agent by the ATRP polymerization process: trifluoroethyl methacrylate monomer, 14g ethyl-alpha-bromopropionate initiator, 14g bipyridine and 480g1 that 100g step (1) is handled well, the 4-dioxane mixes, and adds 20 gram CaCl in 100 gram trash ices 26H 2The stir cryosel that obtains of O is bathed freezingly, vacuumizes, drum nitrogen 5 times is with except oxygen; Then under nitrogen protection, be warming up to 80 ℃, add 20g cuprous chloride reaction 10h, obtain PTFEMA-Br macromole evocating agent solution, record number-average molecular weight Mn=1.57 * 10 by gel permeation chromatography (GPC) method 4, polydispersity coefficient PDI=1.24.Determine this macromole evocating agent structural formula I n=97 according to infrared spectra, NMR (Nuclear Magnetic Resonance) spectrum, GPC data and reaction principle;
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-Br macromole evocating agent to constant weight;
B, with PTFEMA-Br as the synthetic PTFEMA-b-PSt segmented copolymer of ATRP macromole evocating agent:
Described PTFEMA-Br ATRP macromole evocating agent is applied to the ATRP polyreaction and prepares the narrower PTFEMA-b-PSt fluorinated block copolymer of molecular weight distribution, and it may further comprise the steps:
(1) the 5%NaOH aqueous solution and deionized water wash are used respectively in cinnamic processing, and be for subsequent use behind the underpressure distillation purifying behind the anhydrous magnesium sulfate drying;
(2) 100g styrene monomer, 140gPTFEMA-Br ATRP macromole evocating agent and 14g bipyridine and 540g butanone are mixed, in 100 gram trash ices, add 20 gram CaCl 26H 2The stir cryosel that obtains of O is bathed freezingly, vacuumizes, drum nitrogen 4 times to be to remove oxygen; Then under nitrogen protection, be warming up to 110 ℃, add 20g cuprous chloride reaction 11h, obtain the PTFEMA-b-PSt fluorinated block copolymer; Record number-average molecular weight Mn=3.52 * 10 by gel permeation chromatography (GPC) method 4, polydispersity coefficient PDI=1.24;
Figure 198528DEST_PATH_IMAGE002
Figure 141076DEST_PATH_IMAGE002
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-b-PSt fluorinated block copolymer to constant weight.
Embodiment 4
Polymethyl acrylic acid trifluoro ethyl ester (PTFEMA-Br) macromole evocating agent of a, a kind of α-bromine atoms, its chemical structural formula is as shown in the formula shown in the I, and described PTFEMA-Br macromole evocating agent is to be prepared from by the ATRP polymerization process, and concrete operation step is as follows:
(1) processing of trifluoroethyl methacrylate: with deionized water the trifluoroethyl methacrylate monomer is washed till neutrality, then uses successively CaCl 2And CaH 2Soaked respectively 2 days, at last under nitrogen protection and at CaH 2There is lower underpressure distillation purifying, preserves in 0-4 ℃ of sealing, for subsequent use;
(2) prepare the PTFEMA-Br macromole evocating agent by the ATRP polymerization process: trifluoroethyl methacrylate monomer, 20g ethyl-alpha-bromopropionate initiator, 20g bipyridine and 550g butanone that 100g step (1) is handled well mix, and add 20 gram CaCl in 100 gram trash ices 26H 2The stir cryosel that obtains of O is bathed freezingly, vacuumizes, drum nitrogen 4 times is with except oxygen; Then under nitrogen protection, be warming up to 60 ℃, add 0.2g cuprous chloride reaction 4h, obtain PTFEMA-Br macromole evocating agent solution, record number-average molecular weight Mn=7.15 * 10 by gel permeation chromatography (GPC) method 3, polydispersity coefficient PDI=1.22.Determine this macromole evocating agent structural formula I n=40 according to infrared spectra, NMR (Nuclear Magnetic Resonance) spectrum, GPC data and reaction principle;
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-Br macromole evocating agent to constant weight;
B, with PTFEMA-Br as the synthetic PTFEMA-b-PSt segmented copolymer of ATRP macromole evocating agent:
Described PTFEMA-Br ATRP macromole evocating agent is applied to the ATRP polyreaction and prepares the narrower PTFEMA-b-PSt fluorinated block copolymer of molecular weight distribution, and it may further comprise the steps:
(1) the 5%NaOH aqueous solution and deionized water wash are used respectively in cinnamic processing, and be for subsequent use behind the underpressure distillation purifying behind the anhydrous magnesium sulfate drying;
(2) 100g styrene monomer, 200gPTFEMA-Br ATRP macromole evocating agent and 20g bipyridine and 600g butanone are mixed, in 100 gram trash ices, add 20 gram CaCl 26H 2The stir cryosel that obtains of O is bathed freezingly, vacuumizes, drum nitrogen 5 times to be to remove oxygen; Then under nitrogen protection, be warming up to 120 ℃, add 30g cuprous chloride reaction 2h, obtain the PTFEMA-b-PSt fluorinated block copolymer; Record number-average molecular weight Mn=2.32 * 10 by gel permeation chromatography (GPC) method 4, polydispersity coefficient PDI=1.25;
Figure 641328DEST_PATH_IMAGE002
Figure 61945DEST_PATH_IMAGE002
Figure 347564DEST_PATH_IMAGE002
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-b-PSt fluorinated block copolymer to constant weight.

Claims (4)

1. the preparation method of a PTFEMA-b-PSt fluorinated block copolymer is characterized in that, adopts following technical scheme:
A, a kind of end group are polymethyl acrylic acid fluorine ethyl ester (PTFEMA-Br) macromole evocating agent of α-bromine atoms, and its chemical structural formula is as shown in the formula shown in the I:
Figure 2011102067375100001DEST_PATH_IMAGE001
The formula I
N is the natural number of 20-100;
Described PTFEMA-Br macromole evocating agent is to be prepared from by the ATRP polymerization process, and concrete operation step is as follows:
(1) processing of trifluoroethyl methacrylate: with deionized water the trifluoroethyl methacrylate monomer is washed till neutrality, then uses successively CaCl 2And CaH 2Soaked respectively 2 days, at last under nitrogen protection and at CaH 2There is lower underpressure distillation purifying, preserves in 0-4 ℃ of sealing, for subsequent use;
(2) prepare the PTFEMA-Br macromole evocating agent by the ATRP polymerization process: trifluoroethyl methacrylate monomer, 2.0-20 mass parts ethyl-alpha-bromopropionate initiator, 0.2-20 mass parts bipyridine and 300-550 mass parts organic solvent that 100 mass parts steps (1) are handled well mix, it is freezing that cryosel is bathed, and vacuumizes, drum nitrogen 3-5 time to be to remove oxygen; Then under nitrogen protection, be warming up to 60-120 ℃, add 0.2-30 mass parts cuprous chloride reaction 1-10h, obtain PTFEMA-Br macromole evocating agent solution;
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-Br macromole evocating agent to constant weight;
B, with PTFEMA-Br as the synthetic PTFEMA-b-PSt segmented copolymer of ATRP macromole evocating agent:
Described PTFEMA-Br ATRP macromole evocating agent is applied to the ATRP polyreaction and prepares the narrower PTFEMA-b-PSt fluorinated block copolymer of molecular weight distribution, and it may further comprise the steps:
(1) the 5%NaOH aqueous solution and deionized water wash are used respectively in cinnamic processing, and be for subsequent use behind the underpressure distillation purifying behind the anhydrous magnesium sulfate drying;
(2) 100 mass parts styrene monomers, 1-200 mass parts PTFEMA-Br ATRP macromole evocating agent and 0.01-20 mass parts bipyridine and 400-600 mass parts organic solvent are mixed, it is freezing that cryosel is bathed, and vacuumizes, drum nitrogen 3-5 time to be to remove oxygen; Then under nitrogen protection, be warming up to 90-120 ℃, add 0.01-30 mass parts cuprous chloride reaction 2-30h, obtain the PTFEMA-b-PSt fluorinated block copolymer;
Figure 13036DEST_PATH_IMAGE002
Figure 408245DEST_PATH_IMAGE002
Figure 534202DEST_PATH_IMAGE002
(3) after experiment finishes, polymer fluid poured in the beaker that a large amount of methyl alcohol are housed lentamente precipitate, the limit bevelling stirs, and then with polymer filtration, hangs, and transfers to subsequently in the vacuum drying oven and be dried to constant weight under 50 ℃ condition;
(4) polymerisate dissolves with tetrahydrofuran (THF), and solution is through neutral Al 2O 3Copper salt catalyst is removed in post absorption, and filtrate is poured in the methyl alcohol and precipitated, filters, and 50 ℃ of vacuum-dryings of polymkeric substance are collected and obtained the PTFEMA-b-PSt fluorinated block copolymer to constant weight.
2. the preparation method of a kind of PTFEMA-b-PSt fluorinated block copolymer according to claim 1 is characterized in that, the organic solvent described in the step a comprises toluene, Isosorbide-5-Nitrae-dioxane and butanone.
3. the preparation method of a kind of PTFEMA-b-PSt fluorinated block copolymer according to claim 1 is characterized in that, the organic solvent described in the step b comprises Isosorbide-5-Nitrae-dioxane and butanone.
4. the preparation method of a kind of PTFEMA-b-PSt fluorinated block copolymer according to claim 1 is characterized in that, described cryosel is bathed the freezing 20 gram CaCl that refer to add in 100 gram trash ices 26H 2O stirs and obtains.
CN2011102067375A 2011-07-22 2011-07-22 Preparation method of PTFEMA (trifluoroethyl methacrylate)-b-PSt fluorine-containing block copolymer Pending CN102887981A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2011102067375A CN102887981A (en) 2011-07-22 2011-07-22 Preparation method of PTFEMA (trifluoroethyl methacrylate)-b-PSt fluorine-containing block copolymer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2011102067375A CN102887981A (en) 2011-07-22 2011-07-22 Preparation method of PTFEMA (trifluoroethyl methacrylate)-b-PSt fluorine-containing block copolymer

Publications (1)

Publication Number Publication Date
CN102887981A true CN102887981A (en) 2013-01-23

Family

ID=47531672

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2011102067375A Pending CN102887981A (en) 2011-07-22 2011-07-22 Preparation method of PTFEMA (trifluoroethyl methacrylate)-b-PSt fluorine-containing block copolymer

Country Status (1)

Country Link
CN (1) CN102887981A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003016412A1 (en) * 2001-08-14 2003-02-27 Avecia Bv Aqueous crosslinkable coating compositions based on vinyl fluoropolymer
CN101792503A (en) * 2010-02-04 2010-08-04 中科院广州化学有限公司 Fluorinated acrylate atom transfer radical polymerization (ATRP) macromolecule initiator as well as preparation method and application thereof
CN101899126A (en) * 2010-07-21 2010-12-01 常州大学 Miniemulsion with fluorinated block copolymers as co-stabilizers and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003016412A1 (en) * 2001-08-14 2003-02-27 Avecia Bv Aqueous crosslinkable coating compositions based on vinyl fluoropolymer
CN101792503A (en) * 2010-02-04 2010-08-04 中科院广州化学有限公司 Fluorinated acrylate atom transfer radical polymerization (ATRP) macromolecule initiator as well as preparation method and application thereof
CN101899126A (en) * 2010-07-21 2010-12-01 常州大学 Miniemulsion with fluorinated block copolymers as co-stabilizers and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
侯丽华: "以ATRP方法制备含氟嵌段共聚物及其性能研究", 《学位论文 济南大学:高分子化学与物理》 *

Similar Documents

Publication Publication Date Title
CN102964544B (en) Water-dispersible crosslinking type fluoropolymer and application of fluoropolymer in preparation of super-amphiphobic surfaces
CN101792503B (en) Fluorinated acrylate atom transfer radical polymerization (ATRP) macromolecule initiator as well as preparation method and application thereof
CN103709344B (en) Crosslinkable gathers fluoroalkyl-b-polysiloxane and preparation method
CN104045778A (en) Preparation method of star-like hybrid material with UCST and polyhedral oligomeric silsesquioxane (POSS) as core
CN104262555A (en) Block polymer with multi-response property for temperature and carbon dioxide and preparation method thereof
CN101602827A (en) A kind of preparation method of high oil-absorbing resin
CN103724555A (en) Preparation method for thermoplastic elastomer
CN103570886A (en) Organic silicon modified fluorinated acrylate polymer and preparation method thereof
CN106164109A (en) Regulation by the controllable free-radical polymerisation of the acrylate of light
CN104628974B (en) A kind of amphipathic copolymer and preparation method thereof assigning membrane material pH responses
CN104497226A (en) Preparation method of star-shaped hybrid material taking POSS (polyhedral oligomeric silsesquioxane) as core and having UCST (upper critical solution temperature) and UV (ultraviolet) responsiveness
CN105289331B (en) Amphipathic triblock polymer PSxMAAy‑g‑fPEGzModified PVDF ultrafiltration membrane and preparation method thereof
CN104530309A (en) Terminal double-bond free radical copolymerization fluorine-containing large-molecular monomer as well as preparation method and application thereof
CN104592464A (en) Organic and inorganic hybrid block copolymer containing POSS (polyhedral oligomeric silsesquioxane) and zwitter-ion structure and synthesis method of organic and inorganic hybrid block copolymer
CN102964543A (en) Amphiphilic fluorinated acrylate penta-block copolymer and preparation method thereof
CN104031214B (en) A kind of St/MAH-g-MMA graft copolymer and its preparation method and application
CN102887981A (en) Preparation method of PTFEMA (trifluoroethyl methacrylate)-b-PSt fluorine-containing block copolymer
JP4136886B2 (en) Polymers of novel alicyclic vinyl ethers
CN102850474A (en) Method for preparing polymethyl methacrylate by single electron transfer living radical emulsion polymerization
Deng et al. Graft copolymers with polyamide backbones via combination of Passerini multicomponent polymerization and controlled chain-growth polymerization
CN112409552B (en) Photo-induced free radical polymerization method
CN101935382B (en) Methyl methacrylate block copolymer and preparation method thereof
CN104193923A (en) Hydrophobic/oleophobic fluorosilicone triblock polymer and preparation method thereof
CN106046221B (en) The catalyst and polymerization of a kind of reversible-suspend mode free radical polymerization
CN104497227A (en) Preparation method of POSS-cored pH-UV dual-responsiveness starlike block copolymerization material

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20130123