CN101709102A - Perfluorinated resin with high exchange capacity as well as preparation method and application thereof - Google Patents
Perfluorinated resin with high exchange capacity as well as preparation method and application thereof Download PDFInfo
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- Y02E60/30—Hydrogen technology
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Abstract
The invention provides a high exchange capacity perfluorinated resin of two types of short side-radical sulfonyl fluoride with different structures and cyan side-radical. The resin is a polyprotonic copolymer comprising the following components in total molar fraction: 50-85 percent of tetrafluoroethylene polymerization unit, 5-49 percent of the polymerization unit of the two types of short side-radical sulfonyl fluoride vinyl ether with two different structures, and1-10 percent of cyan side-radical vinyl ether polymerization unit. A perfluorinated ion exchange membrane prepared by the resin not only has resistance to various chemical reagents, but also has high ion exchange capacity, electric conductivity, mechanical strength and dimensional stability, low membrane resistance and long service life, and is suitable for usage in fuel cells or high-temperature fuel cells. The invention also provides a preparation method and applications of the resin.
Description
Technical field
The invention belongs to the fluoro-containing macromolecule material field, relate to a kind of high-exchange-capacity perfluorinated resin and preparation method thereof that has, relate in particular to multi-component copolymer perfluorinated ion exchange resin that has short side group sulfonic acid fluoride of two kinds of different structures and cyano group side group and preparation method thereof.
Background technology
After E.I.Du Pont Company was processed into perfluorinated sulfonic resin perfluorinated sulfonic acid type ion-exchange membrane and this film and used in chlorine industry and Proton Exchange Membrane Fuel Cells the seventies in last century, perfluorinated ion exchange resin had obtained extensive studies in countries in the world.
Contain ion-exchange group, the exchange membrane containing fluorine that especially contains sulfonic group and carboxylic acid group is more suitable for being used as the ion-exchange membrane of fuel cell and chlor-alkali electrolytic cells owing to its chemically-resistant degradation property.US3282875 is disclosed first document synthetic about sulfonyl fluoride monomer and the sulfonate resin preparation of E.I.Du Pont Company, employing be emulsion polymerization in the aqueous systems, the functional monomer structure that contains the sulfonic acid fluoride side group is: FO
2SCF
2CF
2OCF (CF
3) CF
2OCF=CF
2, this monomer structure is generally adopted at present.US3560568 be E.I.Du Pont Company disclosed one piece about short side group sulfonyl fluoride monomer and the preparation of sulfonate resin and the patent of performance, the sulfonyl fluoride monomer structure of being reported is FO
2SCF
2CF
2OCF=CF
2, preparation route complexity and yield are lower.Introduced the sulfonate resin by the preparation of novel texture perfluor sulfonyl fluorine monomer among US3884885, the US 3041317, the structure of the sulfonyl fluoride monomer of employing is R
fCF=CFSO
2F, this monomeric reactive behavior is lower.US4358545, US4417969 are the disclosed patents of U.S. Dow chemical company, and this patent relates generally to and adopts short side group monomer (CF
2=CFOCF
2CF
2SO
2F) character and the application of the multipolymer that forms with fluorine-containing vinyl monomer copolymerization such as tetrafluoroethylene, Zhi Bei sulfonate resin is owing to be to adopt solution film-forming by this method, be difficult to prepare film, and the mechanical strength of film is not high enough, described in patent US4661411, US5718947.US4940525 discloses a kind of preparation method who uses the sulfonyl fluoride monomer copolymer resins of vinylidene fluoride monomers and short side group, and this resin has not possessed the perfluor structure, and is less better aspect erosion resistance.Announced the preparation of low EW value sulfonate resin among the EP0289869, the sulfonyl fluoride monomer of employing is the present general monomer structure that adopts, and its EW value is between 575-800.EP1451233 has reported the method by the low EW value resin of miniemulsion preparation.Patent US7022428, US7041409, US6861489 have reported the preparation of the sulfonate resin of low EW value, adopt the mini-emulsion polymerization reaction, and added the monomer that contains diene ether in polymerization process, and diene ether monomer structure is CF
2=CF-O-CF
2CF
2CF
2-OCF=CF
2, the EW value is between 625-850.GB1034197 discloses and has contained sulfonic perfluorinated sulfonic acid polymer, and EP1091435 discloses a kind of structure of block sulfonate resin.Above-mentioned polymkeric substance all is to use tetrafluoroethylene monomer and sulfonic acid fluoride side group alkene ether (such as CF
2=CFOCF
2CF (CF
3) OCF
2CF
2SO
2F) copolymerization or further in above-mentioned polymerization system, introduce monomer component such as the US4940525 that other side groups that do not have ion exchanging function contain two keys, polymerization process can adopt this area technique known, as solution polymerization (US2393967, US3041317 etc.), letex polymerization (US4789717, US4864006 etc.), micro-emulsion polymerization (as US6639011, EP1172382, US5608022 etc.), dispersion polymerization, suspension polymerization, mini-emulsion polymerization (EP1451233) or the like.These polymkeric substance with sulfonic acid fluoride side group can obtain the free sulfonic group through the suitable hydrolysis reaction of sulfonic acid fluoride, are used for fields such as fuel cell, electrolyzer, diffusion dialysis, catalysis, precious metal recovery as ion-exchange membrane.
A most important purposes of perfluorinated sulfonic resin is exactly that it is as the application of mould material in fuel cell, a very important requirement to this class ion-exchange membrane is its ionic conductivity, in order to improve specific conductivity, known a kind of way is to improve the loading capacity of sulfonate resin, but increase along with loading capacity, its mechanical property descends, under the extreme case, and the ion exchange resin of high-exchange-capacity even can be dissolved in the water.Mention among the patent EP0031724: the loading capacity total amount for the film that uses in electric groove will be between 0.5-1.6mmol/g (dried resin), preferred 0.8-1.2mmol/g.If the loading capacity total amount is less than 0.5mmol/g, then the resistivity of film is too high, and bath voltage and energy consumption all can be than higher, can not satisfy industrial applications, if the loading capacity total amount is greater than 1.6mmol/g, then the mechanical property of mould material is bad, and life-span and use aspect are restricted.In order to improve exchange capacity and to reduce the mechanicalness loss of energy as far as possible, the other way is to adopt composite membrane, the way that adopts as US5654109, US5246792 is that bilayer or trilamellar membrane material are compound, inner film has high EW value, bear the physical strength effect, outside film plays the ionic conduction effect for low EW value; US5981097 adopts multilayer different ions exchange capacity film to carry out compound; And US5082472 has adopted the resin compounded of the polytetrafluoroethylporous porous membrane of two-way stretch and low EW value to obtain composite membrane to use.Though these ways have kept the physical strength of film to a certain extent, in the raising of the homogeneity of ionic conduction and specific conductivity, certain shortcoming is arranged still.
For improving the physical strength and the dimensional stability of exchange membrane, resin structure is being carried out in the way of modification, known way has group such as US20020014405, the US6767977 that introducing can be crosslinked in resin structure to introduce diene monomers in resin structure, Chinese patent application numbers 200480033602.1 discloses a kind of way of introducing itrile group in polymerization system, crosslinked by after handling itrile group being carried out, the physical strength of increase film.Chinese patent application numbers 200480033631.8 discloses a kind of cyano group, chlorine, iodo introduced in polymerization system, undertaken crosslinked by electron beam.Existing another way is to shorten the side group of comonomer sulfonic acid fluoride at present, when increasing loading capacity, promote the physical strength of mould material, but US6680346 mentions in patent: by lacking side group sulfonyl fluoride monomer synthetic polymkeric substance because the difference of polymerizing condition can produce cyclization, caused the chain transfer of polyreaction, thereby molecular weight reduces, the mechanical strength of material reduces, and, the lifting of loading capacity and the stability of material have been limited along with short side group sulphonyl monomer and tetrafluoroethylene monomer molar ratio increase the generation that can further promote this class side reaction.
A most important purposes of perfluorinated sulfonic resin be exactly its as the application of mould material in fuel cell, be its chemical stability and intensifier electrode catalyzer anti-carbon monoxide (CO) toxic ability to this class by an important requirement of ion-exchange membrane and the formed membrane electrode of catalyst layer.The working temperature of the fuel cell membrane electrode of current broad research and demonstration is between 25-80 ℃, the poisoning behavior promptly can take place in the catalyst layer that reaches membrane electrode in the 10ppm environment at CO content, in order to overcome the many insoluble difficulties of present low-temperature fuel cell membrane electrode, as improve catalyst activity and utilization ratio, intensifier electrode catalyzer anti-carbon monoxide poisoning performance etc., effective solution is to improve the use temperature of fuel cell, when surpassing 100 ℃, catalyzer can bring up to 1 to the tolerance of CO in the membrane electrode, about 000ppm.The exploitation high temperature proton exchange film can improve the electrical efficiency of fuel cell better, reduces the cost of battery system, adapts to the business-like requirement of fuel cell more.The major country of fuel cell studies begins to drop into lot of manpower and material resources research in the world at present.The known sulfonate resin with long side group sulfonic acid fluoride of fuel cell field can not satisfy the high temperature service requirements at present.
Summary of the invention
One object of the present invention is, a kind of high-exchange-capacity perfluorinated resin is provided, and this high-exchange-capacity perfluorinated resin has the short side group sulfonic acid fluoride and the cyano group side group of two kinds of different structures, has high loading capacity and favorable mechanical performance.Another object of the present invention is, a kind of preparation method of above-mentioned high-exchange-capacity perfluorinated resin is provided.Another purpose of the present invention is, a kind of ion-exchange membrane that is prepared from by above-mentioned high-exchange-capacity perfluorinated resin is provided.A further object of the present invention is, a kind of fuel cell or electrolyzer that comprises above-mentioned ion-exchange membrane is provided.A further object of the present invention is, a kind of purposes of above-mentioned high-exchange-capacity perfluorinated resin is provided.
Above-mentioned purpose of the present invention adopts following technical scheme to realize:
On the one hand, the invention provides a kind of high-exchange-capacity perfluorinated resin, its short side group sulfonic acid fluoride alkene ether monomer by tetrafluoroethylene, two kinds of different structures, a kind of cyano group side group alkene ether monomer multi-component copolymer close and form, and this resin mainly contains with the repeating unit shown in the following formula (I):
The wherein integer of n=0-3, preferably n=0; The integer of m=2-4; The integer of a, b, c=3-15, the integer of a ', b ', c '=1-3; X/ (x+y+z)=0.2-0.7, y/ (x+y+z)=0.2-0.79, z/ (x+y+z)=0.01-0.1.
Preferably, the structural formula of the short side group sulfonic acid fluoride alkene ether monomer of described two kinds of different structures is respectively:
The structural formula of described cyano group side group alkene ether monomer is:
The wherein integer of n=0-3, preferably n=0; The integer of m=2-4.
Preferably, the shared molar content percentage ratio of each polymerized unit is in the described resin: the overall molar fraction in tetrafluoroethylene polymerization unit is 50～85%, the overall molar fraction of short side group sulphonyl fluroxene polymerized unit of two kinds of different structures is 5～49%, and the overall molar fraction of cyano group side group alkene ether polymerized unit is 1～10%.
Preferably, the shared molar content percentage ratio of each polymerized unit is in the described resin: the overall molar fraction in tetrafluoroethylene polymerization unit is 70～80%, the overall molar fraction of short side group sulphonyl fluroxene polymerized unit of two kinds of different structures is 15～29%, and the overall molar fraction of cyano group side group alkene ether polymerized unit is 1～5%.
Preferably, the mol ratio of the short side group sulphonyl fluroxene polymerized unit (1) of two kinds of different structures and (2) is 0.2-0.8: 0.8-0.2 in the described resin; Be preferably 0.4-0.6: 0.6-0.4.
On the other hand, the invention provides the preparation method of above-mentioned high-exchange-capacity perfluorinated resin, this preparation method comprises that the short side group sulfonic acid fluoride alkene ether monomer that makes tetrafluoroethylene, two kinds of different structures, a kind of cyano group side group alkene ether monomer carry out polyreaction under the initiator effect, preferably, the reaction times of described polyreaction is 1～8 hour, temperature of reaction is 10～80 ℃, and reaction pressure is 2～10MPa.
Preferably, described initiator is selected from N
2F
2, in perfluoroalkyl superoxide and the persulphate one or more.
Preferably, described perfluoroalkyl superoxide is to be selected from peroxidation perfluoroalkyl acyl compound, peroxidation perfluoro alkoxy acyl compounds, the fluorine-containing alkyl acyl compound of peroxidation part and the peroxidation part fluoroalkoxy acyl compounds one or more; Described persulphate is to be selected from persulfuric acid ammonium salt, basic metal persulfide and the alkaline-earth metal persulfide one or more.
More preferably, described perfluoroalkyl superoxide for be selected from perfluoro propionyl superoxide, 3-chlorine fluorine propionyl superoxide, perfluor methoxyl group acetyl pexoxide,
-H-perfluor butyryl superoxide,
-SO
2F-perfluor-2,5,8-trimethylammonium-3,6,9-trioxa-undecyl superoxide, CF
3CF
2CF
2CO-OO-COCF
2CF
2CF
3, CF
3CF
2CF
2OCFCF
3CO-OO-COCFCF
3OCF
2CF
2CF, CF
3CF
2CH
2CO-OO-COCH
2CF
2CF
3And CF
3OCF
2CF
2CO-OO-COCF
2CF
2OCF
3In one or more; Described persulphate is to be selected from ammonium persulphate and the Potassium Persulphate one or more.
Preferably, described preparation method also is included in the step that aqueous phase carries out emulsion polymerization.
Preferably, in the emulsion polymerization step, emulsifying agent is selected from anionic emulsifier, for example sodium soap, sodium lauryl sulphate, alkyl sodium sulfonate and sodium alkylarysulfonate; And nonionic emulsifier, alkyl phenol polyether alcohols for example is as in polyoxyethylene nonylphenol ether, polyoxyethylene fatty acid and the polyoxyethylene fatty acid ether one or more.
More preferably, in the emulsion polymerization step, the mass percent concentration of emulsifying agent in water is 0.1-20%, the mass percent concentration of short side group sulfonic acid fluoride alkene ether monomer in water of two kinds of different structures is 5-30%, and the mass percent concentration of cyano group side group alkene ether monomer in water is 1～12%.
Another aspect the invention provides a kind of ion-exchange membrane that is prepared from by above-mentioned high-exchange-capacity perfluorinated resin.
On the one hand, the invention provides a kind of fuel cell or electrolytic cell device that comprises above-mentioned ion-exchange membrane again; Described fuel cell is preferably proton membrane fuel battery or high-temperature fuel cell, more preferably the high temperature proton membrane fuel battery; Described electrolyzer is preferably chlor-alkali electrolysis cell.
On the one hand, the invention provides the purposes that above-mentioned high-exchange-capacity perfluorinated resin is used to make fuel cell or electrolytic cell device intermediate ion exchange membrane again; Described fuel cell is preferably proton membrane fuel battery or high-temperature fuel cell, more preferably the high temperature proton membrane fuel battery; Described electrolyzer is preferably chlor-alkali electrolysis cell; Preferably, before the use, earlier that the cyano group side group is crosslinked by the chemical process cyclisation.
Compared with prior art, the present invention has the following advantages at least:
1, perfluorinated resin of the present invention has the short side group sulfonic acid fluoride and the cyano group side group of two kinds of different structures, solved the opposed contradiction of prior art intermediate ion exchange capacity and physical strength, the perfluorinated resin that has high loading capacity and favorable mechanical performance simultaneously is provided.
2, perfluorinated resin of the present invention has the short side group sulfonic acid fluoride and the cyano group side group of two kinds of different structures, solved short side group sulfonic acid fluoride alkene ether monomer chain transfer reaction has taken place in polymerization process, the not high enough problem of molecular resin amount that obtains, concrete reaction mechanism can be as follows: one, adopted two kinds of short side group sulfonic acid fluoride alkene ether monomers with different structure in the polymerization process, these two kinds of monomers act synergistically mutually; Its two, have cyano group alkene ether in the polymerization system, interact with other two kinds of alkene ether monomers when participating in polyreaction, the existence of these different sorts alkene ethers makes polyreaction work in coordination with to carry out to the high molecular direction, eliminated the chain transfer cyclization.
3, the present invention adopts tetrafluoroethylene (TFE) and two kinds of short side group sulfonic acid fluoride alkene ether monomer and cyano group side group alkene ether monomers that have different structure to carry out multi-component copolymer, obtain high molecular high-exchange-capacity perfluorinated resin, this multiple copolymer has high chemical stability, high loading capacity and good high-temperature mechanical stability.
The perfluorinated resin of high-exchange-capacity of the present invention can be used for preparing the ion-exchange membrane of devices such as fuel cell (for example high-temperature fuel cell) and chlor-alkali electrolytic cells.The mould material of using this resins has high current efficiency, low membrane resistance, high dimensional stability and higher physical strength.
Below be detailed description of the present invention:
The invention provides a kind of short side group sulfonic acid fluoride of two kinds of different structures and high-exchange-capacity perfluorinated resin of cyano group side group of having, this perfluorinated resin is closed and is formed by the short side group sulfonic acid fluoride alkene ether monomer of tetrafluoroethylene, two kinds of different structures, a kind of cyano group side group alkene ether monomer multi-component copolymer, and the molecular formula of polymer chain is:
The wherein integer of n=0-3, preferably n=0; The integer of m=2-4; The integer of a, b, c=3-15, the integer of a ', b ', c '=1-3; X/ (x+y+z)=0.2-0.7, y/ (x+y+z)=0.2-0.79, z/ (x+y+z)=0.01-0.1.
The shared molar content percentage ratio of various polymerized units in the polymkeric substance: the overall molar fraction in tetrafluoroethylene polymerization unit is 50～85%, the overall molar fraction of short side group sulphonyl fluroxene polymerized unit of two kinds of different structures is 5～49%, and the overall molar fraction of cyano group side group alkene ether polymerized unit is 1～10%.
Preferably, the shared molar content percentage ratio of various polymerized units in the polymkeric substance: the overall molar fraction in tetrafluoroethylene polymerization unit is 70～80%, the overall molar fraction of sulfonic acid fluoride side group alkene ether polymerized unit of two kinds of different structures is 15～29%, and the overall molar fraction of cyano group side group alkene ether polymerized unit is 1～5%.
The structural formula of the short side group sulfonic acid fluoride alkene ether monomer of described two kinds of different structures is respectively:
The structural formula of described cyano group side group alkene ether monomer is:
N=0-3 in the formula, preferably n=0; The integer of m=2-4.
The number-average molecular weight of above-mentioned high-exchange-capacity perfluorinated resin is 10～600,000, is preferably 15～300,000, most preferably is 18-25 ten thousand.The molecular weight distribution numerical value of above-mentioned high-exchange-capacity perfluorinated resin (being meant that weight-average molecular weight is than number-average molecular weight) is 1.5-2.0.
The invention provides the preparation method of the perfluorinated ion exchange resin of above-mentioned short side group sulfonic acid fluoride that has two kinds of different structures and cyano group side group, this preparation method be the short side group sulfonic acid fluoride alkene ether monomer by tetrafluoroethylene, two kinds of different structures, a kind of cyano group side group alkene ether monomer 10～80 ℃, under action of evocating, carry out copolyreaction (polyreaction) and prepare, the reaction times of this copolyreaction is 1～8 hour, and reaction pressure is 2～10MPa.
Among the above-mentioned preparation method, initiator can use initiator well known in the art, also can use homemade initiator.
Described initiator is selected from: N
2F
2, perfluoroalkyl superoxide or persulphate.
Preferably, described perfluoroalkyl superoxide comprises: peroxidation perfluoroalkyl acyl compound, peroxidation perfluoro alkoxy acyl compounds, the fluorine-containing alkyl acyl compound of peroxidation part and peroxidation part fluoroalkoxy acyl compounds.More preferably, described perfluoroalkyl superoxide be perfluoro propionyl superoxide, 3-chlorine fluorine propionyl superoxide, perfluor methoxyl group acetyl pexoxide,
-H-perfluor butyryl superoxide,
-SO
2F-perfluor-2,5,8-trimethylammonium-3,6,9-trioxa-undecyl superoxide, CF
3CF
2CF
2CO-OO-COCF
2CF
2CF
3, CF
3CF
2CF
2OCFCF
3CO-OO-COCFCF
3OCF
2CF
2CF
3, CF
3CF
2CH
2CO-OO-COCH
2CF
2CF
3Or CF
3OCF
2CF
2CO-OO-COCF
2CF
2OCF
3
Preferably, described persulphate comprises persulfuric acid ammonium salt, basic metal persulfide or alkaline-earth metal persulfide; More preferably, described persulphate is ammonium persulphate or Potassium Persulphate etc.
Preferably, the mol ratio of the short side group sulphonyl fluroxene polymerized unit of tetrafluoroethylene polymerization unit, two kinds of different structures and cyano group side group alkene ether polymerized unit is in the resin: 50～85: 5～49: 1～10.
Preferably, the short side group sulphonyl fluroxene polymerized unit (1) of two kinds of different structures and (2) the mol ratio 0.2-0.8 in resin: 0.8-0.2; More preferably, the short side group sulphonyl fluroxene polymerized unit (1) of two kinds of different structures and (2) mol ratio in resin are 0.4-0.6: 0.6-0.4.
Preferably, above-mentioned copolyreaction is carried out letex polymerization at aqueous phase, and concrete emulsion polymerization is as follows:
1) reactor is cleaned after, two kinds short side group sulfonic acid fluoride alkene ether monomers, cyano group side group alkene ether monomer and emulsifying agents adding pure water, different ratios, the oeverall quality percentage concentration of emulsifying agent in water is 0.1-20%, the mass percent concentration of two kinds short side group sulphonyl fluroxenes in water is 5-30%, and the mass percent concentration of cyano group side group alkene ether monomer in water is 1～12%;
Wherein, described emulsifying agent comprises anionic emulsifier and nonionic emulsifier.Described anionic emulsifier comprises sodium soap, sodium lauryl sulphate, alkyl sodium sulfonate, sodium alkylarysulfonate etc.; Described nonionic emulsifier comprises the alkyl phenol polyether alcohols, as polyoxyethylene nonylphenol ether, polyoxyethylene fatty acid, polyoxyethylene fatty acid ether.Mentioned emulsifier can use separately also can multiple composite use.
2) filling tetrafluoroethylene monomer to pressure by the aerometer measuring tank in reactor is 2-10MPa;
3) reactor is warming up to 10～80 ℃, adds the initiator initiation reaction by volume pump in reaction system and carries out, and continues to add tetrafluoroethylene monomer and initiator to reactor, keeps reactor reaction pressure 2-10MPa, and the reaction times is 1～8 hour;
When 4) reaction finishes, stop in reactor, to add initiator and tetrafluoroethylene monomer, reclaim unreacted tetrafluoroethylene monomer by reactor blowdown piping and accumulator tank emptying; Obtain milky polymer paste, liquid slurry is entered in the finishing apparatus by material drain system, high speed shear, filtering separation obtains the white polymer powder, in 100 ℃ of baking ovens, dry, obtain having the short side group sulfonic acid fluoride of two kinds of different structures and the high-exchange-capacity perfluorinated resin of cyano group side group.Sulfonic acid fluoride alkene ether monomer in the filtered liquid and cyano group side group alkene ether monomer are recycled by recovery system.
In the above-mentioned polyreaction, described initiator is selected from: N
2F
2, perfluoroalkyl superoxide or persulphate; Those skilled in the art can select initiator concentration according to the common practise of this area.
Described perfluoroalkyl superoxide comprises: peroxidation perfluoroalkyl acyl compound, peroxidation perfluoro alkoxy acyl compounds, the fluorine-containing alkyl acyl compound of peroxidation part or peroxidation part fluoroalkoxy acyl compounds.
Described persulphate comprises ammonium persulphate, alkali metal persulphate or alkaline-earth metal persulphate; Initiator system of ammonium persulfate or Potassium Persulphate.
Of the present inventionly have the short side group sulfonic acid fluoride of two kinds of different structures and the high-exchange-capacity perfluorinated resin of cyano group side group can be used for making fuel cell, for example the ion-exchange membrane of high-temperature fuel cell.
The high-exchange-capacity perfluorinated resin of short side group sulfonic acid fluoride that has two kinds of different structures of the present invention and cyano group side group can be used in the devices such as proton membrane fuel battery (for example high temperature proton membrane fuel battery) or chlor-alkali electrolytic cells as ion-exchange membrane.This class ion-exchange membrane has high chemical stability, high current efficiency, low membrane resistance, high dimensional stability and higher physical strength etc.
The high-exchange-capacity perfluorinated resin of short side group sulfonic acid fluoride that has two kinds of different structures of the present invention and cyano group side group can adopt solution casting technology to make the perfluorinated sulfonic acid ion exchange membrane of suitable thickness or employing to melt extrude equipment and extrude the mould material of preparing suitable thickness by high-temperature fusion.Then that mould material is crosslinked by known way such as radiation crosslinking, thermal treatment, add light trigger and cause crosslinked or cause by radical initiator that crosslinked that the cyano group side group is carried out cyclisation is crosslinked; Sulfonic acid fluoride side group made the transition and be sulfonic acid lateral group thereafter, the perfluorinated ion-exchange membrane of making not only has anti-various chemical mediator, also have high electroconductibility, high mechanical strength and high dimensional stability, low membrane resistance is highly suitable in fuel cell, high-temperature fuel cell or the chlor-alkali electrolysis cell and uses.
When the high-exchange-capacity perfluorinated resin of short side group sulfonic acid fluoride that has two kinds of different structures of the present invention and cyano group side group is used in fuel cell, based on crosslinked water retention capacity, dimensional stability and the physical strength that can further improve ion-exchange membrane of cyano group side group cyclisation, effectively improve the usability of mould material, further increase the time limit of service of mould material.
The invention has the beneficial effects as follows:
The loading capacity of institute of the present invention synthetic perfluorinated ion exchange resin is between 0.5-2.6mmol/g (dried resin), loading capacity is more little, its physical strength is big more, wherein loading capacity surpasses 20MPa between the physical strength of the uncrosslinked resin of 1.28-1.95mmol/g, the mould material of preparation has extraordinary thermal stability, mould material is through after the crosslinking Treatment, and its physical strength surpasses 30MPa.The specific conductivity of room temperature measuring mould material is greater than 0.2S/cm, and the specific conductivity of measuring under 100 ℃, 45% humidity situation still is higher than 0.05S/cm, can satisfy the demand of fuel cell proton film and chloric alkali electrolysis mould material fully.
Description of drawings
Figure 1A and Figure 1B represent the F of the perfluorinated resin of an embodiment of the invention respectively
19NMR collection of illustrative plates and infared spectrum;
Fig. 2 represents the F of the perfluorinated resin of an embodiment of the invention
19The NMR collection of illustrative plates;
Fig. 3 represents the infared spectrum of the perfluorinated resin of an embodiment of the invention;
Fig. 4 represents the F of the perfluorinated resin of an embodiment of the invention
19The NMR collection of illustrative plates.
Embodiment
Following examples are to further specify of the present invention, but the present invention is not limited thereto.If no special instructions, used reactor is 10L stainless steel autoclave among each embodiment, and is furnished with temperature sensor, pressure transmitter, heating circulation system, cooling recirculation system, agitator motor, inner water-cooled tube, microprocessor pump drive, gas feed valve, liquid feeding valve and material in reactor discharging valve.
Do not have outside the special instruction in following examples, loading capacity all is that sulfonic acid fluoride is hydrolyzed to the result who measures behind the sulfonic acid.
The perfluoroalkyl initiator that the present invention is adopted in building-up process can prepare according to techniques well known, and the preparation method that the present invention recommends is referring to J.Org.Chem., and 1982,47 (11): 2009-2013.
The Potassium Persulphate that the present invention is adopted in building-up process, ammonium persulphate, N
2F
2Gas all can be bought and obtain.Wherein, Potassium Persulphate, ammonium persulphate can pass through the traditional Chinese medicines institutional purchase.N
2F
2Gas can be bought in Eastern Mountain chemical industry company limited and obtain.
The comonomer tetrafluoroethylene that the present invention is adopted in building-up process, short side group sulfonic acid fluoride alkene ether monomer, cyano group side group alkene ether monomer can be bought and obtain, and also can prepare by approach well known.Wherein, tetrafluoroethylene monomer of the present invention is available from Shandong Dongyue Polymer Material Co., Ltd.; Short side group sulfonyl fluoride monomer can obtain with reference to the preparation method described in US3560568 and the US6624328, and short side group sulfonyl fluoride monomer of the present invention adopts Chinese patent application number to be: the method described in CN200910229444.1, CN200910229446.0, the CN 200910230218.5 prepares; Cyano group side group alkene ether monomer can obtain with reference to the preparation method described in US3641104 and the US3852326, and cyano group side group alkene ether monomer of the present invention adopts Chinese patent application number to be: the method described in the CN 200910230075.8 prepares.
Embodiment 1
Reactor is cleaned and adding 5.0L deionized water, 100g Sodium dodecylbenzene sulfonate and 125g polyoxyethylene nonylphenol ether NP-10 emulsifying agent, start whipping appts, vacuumize and fill high pure nitrogen displacement three times, after tested in the reactor oxygen level after below the 1ppm, vacuumize, in reactor, add 500g sulfonic acid fluoride side group alkene ether monomer (1) (F by the liquid feeding valve
2C=CF-O-CF
2-CF
2-SO
2F) and 650g sulfonic acid fluoride side group alkene ether monomer (2) (F
2C=CF-O-CF
2-CF
2-CF
2CF
2-SO
2F) and 405g cyano group side group alkene ether monomer (F
2C=CF-O-CF
2CF
2-CN) after, filling tetrafluoroethylene monomer to pressure in reactor is 2.9MPa, is warming up to 20 ℃, adds 2.6g peroxidation perfluor butyryl radicals compound (CF with volume pump
3CF
2CF
2CO-OO-CCF
2CF
2CF
3) initiated polymerization, continue to feed tetrafluoroethylene (CF
2=CF
2) monomer keeps reaction pressure at 2.9MPa, adds initiator 0.75g every 15min in system, behind the reaction 2h, stops to add initiator, allow react proceed 15min after, stop to add tetrafluoroethylene monomer.Lower the temperature to reactor by cooling recirculation system, reclaim unreacted tetrafluoroethylene monomer by recovery system simultaneously, oyster white slurry in the still is put into after-treatment system by following dispensing valve, after high speed shear, filtering separation obtains the white polymer powder, in 100 ℃ of baking ovens, dry, obtain having the perfluorinated ion exchange resin of short side group sulfonic acid fluoride and cyano group side group.Sulfonic acid fluoride alkene ether monomer in the filtered liquid and cyano group side group alkene ether monomer reclaim the back recycling by recovery system.
Polymer data: through F
19NMR, IR analyze and turn out to be multiple copolymer, the molecular fraction that contains tetrafluoroethylene monomer by fluorine nuclear-magnetism integrated value as can be known in the polymer architecture is 62.71%, containing sulfonic acid fluoride side group alkene ether monomer (1) molecular fraction is 16.5%, containing sulfonic acid fluoride side group alkene ether monomer (2) molecular fraction is 16.3%, containing cyano group side group alkene ether monomer molecular fraction is 4.49%, and overall loading capacity is: the 1.77mmol/g dried resin.Decomposition temperature (T under the TGA test resin nitrogen atmosphere
d) be 403 ℃; IR spectrogram: 1468cm
-1Be S=O vibration absorption peak in the sulfonic acid fluoride; 2272cm
-1The place is-the CN vibration absorption peak; 1200 and two absorptions the strongest of 1148cm-1 cause by CF vibration; 720cm
-1, 641cm
-1Cause by the TFE vibration.
Embodiment 2
Reactor cleaned and add 5.0L deionized water, 220g Sodium dodecylbenzene sulfonate, start whipping appts, vacuumize and fill high pure nitrogen displacement three times, after tested in the reactor oxygen level after below the 1ppm, vacuumize, in reactor, add 500g sulfonic acid fluoride side group alkene ether monomer (1) (F by the liquid feeding valve
2C=CF-O-CF
2-CF
2-SO
2F) and 405g sulfonic acid fluoride side group alkene ether monomer (2) (F
2C=CF-O-CF
2CF
2CF
2CF
2-SO
2F) and 225g cyano group side group alkene ether monomer (F
2C=CF-O-CF
2CF
2CF
2CN) after, filling tetrafluoroethylene monomer to pressure in reactor is 2.9MPa, is warming up to 35 ℃, adds 8.0g peroxidation perfluor propoxy-propylated compound (CF with volume pump
3CF
2CF
2OCF (CF
3) CO-OO-CCF (CF
3) OCF
2CF
2CF
3) initiated polymerization, continue to feed tetrafluoroethylene (CF
2=CF
2) monomer keeps reaction pressure at 2.9MPa, adds initiator 2.3g every 25min in system, behind the reaction 2.5h, stops to add initiator, allow react proceed 25min after, stop to add tetrafluoroethylene monomer.Lower the temperature to reactor by cooling recirculation system, reclaim unreacted tetrafluoroethylene monomer by recovery system simultaneously, oyster white slurry in the still is put into after-treatment system by following dispensing valve, after high speed shear, filtering separation obtains the white polymer powder, in 100 ℃ of baking ovens, dry, obtain having the perfluorinated ion exchange resin of short side group sulfonic acid fluoride and cyano group side group.Sulfonic acid fluoride alkene ether monomer in the filtered liquid and cyano group side group alkene ether monomer reclaim the back recycling by recovery system.
Polymer data: through F
19NMR (shown in Figure 1A), IR (shown in Figure 1B) analyze and turn out to be multiple copolymer, the molecular fraction that contains tetrafluoroethylene monomer by fluorine nuclear-magnetism integrated value as can be known in the polymer architecture is 73.8%, containing sulfonic acid fluoride side group alkene ether monomer (1) molecular fraction is 15%, containing sulfonic acid fluoride side group alkene ether monomer (2) molecular fraction is 9%, containing cyano group side group alkene ether monomer molecular fraction is 2.2%, and overall loading capacity is: the 1.53mmol/g dried resin.Decomposition temperature (T under the TGA test resin nitrogen atmosphere
d) be 402 ℃; IR spectrogram: 1468cm
-1Be S=O vibration absorption peak in the sulfonic acid fluoride; 2272cm
-1The place is-the CN vibration absorption peak; 1200 and 1148cm
-1Two absorptions the strongest are caused by the CF vibration; 720cm
-1, 641cm
-1Cause by the TFE vibration.
Embodiment 3
Reactor is cleaned and adding 5.0L deionized water, 120g Sodium dodecylbenzene sulfonate and 95g polyoxyethylene nonylphenol ether NP-10 emulsifying agent, start whipping appts, vacuumize and fill high pure nitrogen displacement three times, after tested in the reactor oxygen level after below the 1ppm, vacuumize, in reactor, add 300g sulfonic acid fluoride side group alkene ether monomer (1) (F by the liquid feeding valve
2C=CF-O-CF
2-CF
2-SO
2F) and 610g sulfonic acid fluoride side group alkene ether monomer (2) (F
2C=CF-O-CF
2-CF
2CF
2CF
2-SO
2F) and 250g cyano group side group alkene ether monomer (F
2C=CF-O-CF
2CF
2CF
2CF
2CN) after, filling tetrafluoroethylene monomer to pressure in reactor is 3.2MPa, is warming up to 80 ℃, adds 10% ammonium persulfate aqueous solution 320g initiated polymerization with volume pump, continues to feed tetrafluoroethylene (CF
2=CF
2) monomer keeps reaction pressure at 3.2MPa, behind the reaction 3h, stops to add tetrafluoroethylene monomer.Lower the temperature to reactor by cooling recirculation system, reclaim unreacted tetrafluoroethylene monomer by recovery system simultaneously, oyster white slurry in the still is put into after-treatment system by following dispensing valve, after high speed shear, filtering separation obtains the white polymer powder, in 100 ℃ of baking ovens, dry, obtain having the perfluorinated ion exchange resin of short side group sulfonic acid fluoride, cyano group side group.Sulfonic acid fluoride alkene ether monomer in the filtered liquid and cyano group side group alkene ether monomer reclaim the back recycling by recovery system.
Polymer data: through F
19NMR (as shown in Figure 2), IR analyze and turn out to be multiple copolymer, the molecular fraction that contains tetrafluoroethylene monomer by fluorine nuclear-magnetism integrated value as can be known in the polymer architecture is 75.7%, containing sulfonic acid fluoride side group alkene ether monomer (1) molecular fraction is 8.9%, containing sulfonic acid fluoride side group alkene ether monomer (2) molecular fraction is 12.28%, containing cyano group side group alkene ether monomer molecular fraction is 3.12%, and overall loading capacity is: the 1.34mmol/g dried resin.Decomposition temperature (T under the TGA test resin nitrogen atmosphere
d) be 397 ℃; IR spectrogram: 1468cm
-1Be S=O vibration absorption peak in the sulfonic acid fluoride; 2272cm
-1The place is-the CN vibration absorption peak; 984cm
-1For-CF
3Vibration causes; 1200 and 1148cm
-1Two absorptions the strongest are caused by the CF vibration; 720cm
-1, 641cm
-1Cause by the TFE vibration.
Reactor is cleaned and adding 5.0L deionized water, 180g Sodium dodecylbenzene sulfonate and 45g polyoxyethylene nonylphenol ether NP-10 emulsifying agent, start whipping appts, vacuumize and fill high pure nitrogen displacement three times, after tested in the reactor oxygen level after below the 1ppm, vacuumize, in reactor, add 300g sulfonic acid fluoride side group alkene ether monomer (1) (F by the liquid feeding valve
2C=CF-O-CF
2-CF
2-SO
2F) and 400g sulfonic acid fluoride side group alkene ether monomer (2) (F
2C=CF-O-CF
2-CF
2CF
2CF
2-SO
2F) and 250g cyano group side group alkene ether monomer (F
2C=CF-O-CF
2CF (CF
3) OCF
2CF
2CN) after, filling tetrafluoroethylene monomer to pressure in reactor is 2.7MPa, is warming up to 20 ℃, introduces by N in reactor with the gas meter dominant discharge
2F
2Initiated polymerization continues to feed tetrafluoroethylene (CF
2=CF
2) monomer, keep reaction pressure slowly to rise from 2.7MPa, continue in system, to add initiator N
2F
2, the reaction 2h after, reactor pressure is 3.0MPa, stops to add initiator, allow the reaction proceed 1min after, stop to add tetrafluoroethylene monomer.Lower the temperature to reactor by cooling recirculation system, reclaim unreacted tetrafluoroethylene monomer by recovery system simultaneously, oyster white slurry in the still is put into after-treatment system by following dispensing valve, after high speed shear, filtering separation obtains the white polymer powder, in 100 ℃ of baking ovens, dry, obtain having the perfluorinated ion exchange resin of short side group sulfonic acid fluoride and cyano group side group.Sulfonic acid fluoride alkene ether monomer in the filtered liquid and cyano group side group alkene ether monomer reclaim the back recycling by recovery system.
Polymer data: through F
19NMR, IR (as shown in Figure 3) analyze and turn out to be multiple copolymer, the molecular fraction that contains tetrafluoroethylene monomer by fluorine nuclear-magnetism integrated value as can be known in the polymer architecture is 74.5%, containing sulfonic acid fluoride side group alkene ether monomer (1) molecular fraction is 10.5%, containing sulfonic acid fluoride side group alkene ether monomer (2) molecular fraction is 13.79%, containing cyano group side group alkene ether monomer molecular fraction is 1.21%, and overall loading capacity is: the 1.54mmol/g dried resin.Decomposition temperature (T under the TGA test resin nitrogen atmosphere
d) be 388 ℃; IR spectrogram: 1468cm
-1Be S=O vibration absorption peak in the sulfonic acid fluoride; 2272cm
-1The place is-the CN vibration absorption peak; 1200 and 1148cm
-1Two absorptions the strongest are caused by the CF vibration; 720cm
-1, 641cm
-1Cause by the TFE vibration.
Embodiment 5
Reactor cleaned and add 5.0L deionized water, 215g Sodium dodecylbenzene sulfonate emulsifying agent, start whipping appts, vacuumize and fill high pure nitrogen displacement three times, after tested in the reactor oxygen level after below the 1ppm, vacuumize, in reactor, add 780g sulfonic acid fluoride side group alkene ether monomer (1) (F by the liquid feeding valve
2C=CF-O-CF
2-CF
2-SO
2F) and 720g sulfonic acid fluoride side group alkene ether monomer (2) (F
2C=CF-O-CF
2-CF
2CF
2CF
2-SO
2F) and 650g cyano group side group alkene ether monomer (F
2C=CF-O-CF
2CF
2CN) after, filling tetrafluoroethylene monomer to pressure in reactor is 2.8MPa, is warming up to 25 ℃, introduces by N in reactor with the gas meter dominant discharge
2F
2Initiated polymerization continues to feed tetrafluoroethylene (CF
2=CF
2) monomer, keep reaction pressure slowly to rise from 2.8MPa, continue in system, to add initiator N
2F
2, the reaction 2h after, reaction pressure is 3.2MPa, stops to add initiator, allow the reaction proceed 1min after, stop to add tetrafluoroethylene monomer.Lower the temperature to reactor by cooling recirculation system, reclaim unreacted tetrafluoroethylene monomer by recovery system simultaneously, oyster white slurry in the still is put into after-treatment system by following dispensing valve, after high speed shear, filtering separation obtains the white polymer powder, in 100 ℃ of baking ovens, dry, obtain having the perfluorinated ion exchange resin of short side group sulfonic acid fluoride and cyano group side group.Sulfonic acid fluoride alkene ether monomer in the reaction liquid and cyano group side group alkene ether monomer reclaim the back recycling by recovery system.
Polymer data: through F
19NMR (as shown in Figure 4), IR analyze and turn out to be multiple copolymer, the molecular fraction that contains tetrafluoroethylene monomer by fluorine nuclear-magnetism integrated value as can be known in the polymer architecture is 67.1%, containing sulfonic acid fluoride side group alkene ether monomer (1) molecular fraction is 14.2%, containing sulfonic acid fluoride side group alkene ether monomer (2) molecular fraction is 11.46%, containing cyano group side group alkene ether monomer molecular fraction is 7.24%, and overall loading capacity is: the 1.44mmol/g dried resin.Decomposition temperature (T under the TGA test resin nitrogen atmosphere
d) be 385 ℃; IR spectrogram: 1468cm
-1Be S=O vibration absorption peak in the sulfonic acid fluoride; 2272cm
-1The place is-the CN vibration absorption peak; 984cm
-1For-CF
3Vibration causes; 1200 and 1148cm
-1Two absorptions the strongest are caused by the CF vibration; 720cm
-1, 641cm
-1Cause by the TFE vibration.
Embodiment 6
Reactor cleaned and add 5.0L deionized water, 225g Sodium dodecylbenzene sulfonate emulsifying agent, start whipping appts, vacuumize and fill high pure nitrogen displacement three times, after tested in the reactor oxygen level after below the 1ppm, vacuumize, in reactor, add 420g sulfonic acid fluoride side group alkene ether monomer (1) (F by the liquid feeding valve
2C=CF-O-CF
2-CF
2-SO
2F) and 265g sulfonic acid fluoride side group alkene ether monomer (2) (F
2C=CF-O-CF
2-CF
2CF
2CF
2-SO
2F) and 350g cyano group side group alkene ether monomer (F
2C=CF-O-CF
2CF
2CF
2CF
2CN) after, filling tetrafluoroethylene monomer to pressure in reactor is 5.2MPa, is warming up to 45 ℃, adds 20.2g with volume pump
-SO2F-perfluor-2,5,8-trimethylammonium-3,6,9-trioxa-undecyl peroxide polymerization initiator reaction continues to feed tetrafluoroethylene (CF
2=CF
2) monomer keeps reaction pressure at 5.2MPa, adds initiator 6g every 45min in system, behind the reaction 2h, stops to add initiator, allow react proceed 45min after, stop to add tetrafluoroethylene monomer.Lower the temperature to reactor by cooling recirculation system, reclaim unreacted tetrafluoroethylene monomer by recovery system simultaneously, oyster white slurry in the still is put into after-treatment system by following dispensing valve, after high speed shear, filtering separation obtains the white polymer powder, in 100 ℃ of baking ovens, dry, obtain having the perfluorinated ion exchange resin of short side group sulfonic acid fluoride and cyano group side group.Sulfonic acid fluoride alkene ether monomer in the filtered liquid and cyano group side group alkene ether monomer reclaim the back recycling by recovery system.
Polymer data: through F
19NMR, IR analyze and turn out to be multiple copolymer, the molecular fraction that contains tetrafluoroethylene monomer by fluorine nuclear-magnetism integrated value as can be known in the polymer architecture is 80%, containing sulfonic acid fluoride side group alkene ether monomer (1) molecular fraction is 8.2%, containing sulfonic acid fluoride side group alkene ether monomer (2) molecular fraction is 9.92%, containing cyano group side group alkene ether monomer molecular fraction is 1.88%, and overall loading capacity is: the 1.27mmol/g dried resin.Decomposition temperature (T under the TGA test resin nitrogen atmosphere
d) be 389 ℃; IR spectrogram: 1468cm
-1Be S=O vibration absorption peak in the sulfonic acid fluoride; 2272cm
-1The place is-the CN vibration absorption peak; 1200 and 1148cm
-1Two absorptions the strongest are caused by the CF vibration; 720cm
-1, 641cm
-1Cause by the TFE vibration.
Embodiment 7
Present embodiment is used to illustrate that the perfluorinated ion exchange resin that uses embodiment 1-6 prepares the process of ion-exchange membrane, and the mechanical property of prepared film.
The preparation process of ion-exchange membrane:
Pellet preparation: respectively the white powder product that obtains among the embodiment 1-6 is melt extruded machine and extrudes the preparation pellet through small-sized, the extrusion temperature that melt extrudes machine is set at: 250 ℃ in screw rod one district, 255 ℃ in screw rod two districts, 260 ℃ in screw rod three districts, 270 ℃ of forcing machine die orifice temperature, extruding dies diameter 3mm, by adjusting shearing rate, the transparent material of the column that will melt extrude is sheared the transparent resin pellet of preparing length 2-4mm, with pellet with the airtight preservation of double-deck PE plastics bag.
Melt extrude crowded film: will melt extrude machine mouth mould and be replaced by the film extrusion die, screw rod zone design temperature is the same, adopt the mode that melt extrudes to be prepared into film the transparent pellet of preparation, film thickness can be regulated by the width of adjusting die orifice, and the film thickness of preparation is 20-100 μ m usually.
Melt extruding mould makes the transition: with the sulfonic acid fluoride (SO of film
2F) side group transfers azochlorosulfonate acid ion (SO to
3H) form is passed through the sodium hydroxide solution of 80 ℃ of mass percentage concentration 30%, the sulphuric acid soln (H of 30 ℃ of mass percent concentrations 30% successively with the film for preparing
2SO
4), mobile deionized water wash groove.Film in alkali lye residence time 30min, the residence time is 10min in sulphuric acid soln, in the deionization tank, use deionized water rinsing 10min, thereafter with the mould material rolling, airtight preservation, promptly obtain the film product, by the ion-exchange membrane of the perfluorinated ion exchange resin of embodiment 1-6 preparation respectively correspondingly note make film 1-film 6.
The film dynamic performance test: test mode employing method is GB/T1040-92, measure and use the perfluorinated ion exchange resin of embodiment 1-6 preparation to prepare ion-exchange membrane 1-film 6, and the model of E.I.Du Pont Company is the mechanical property of the sulfonate film of NRE 211, the results are shown in table 1.
Table 1
Data by table 1 are compared with the ion-exchange membrane that is purchased that this area is commonly used as can be seen, and the film product of resins of the present invention has better mechanical property.
Embodiment 8
The 1.0L reactor is cleaned and adding 500ml deionized water, 10g Sodium dodecylbenzene sulfonate and 13g polyoxyethylene nonylphenol ether NP-10 emulsifying agent, start whipping appts, vacuumize and fill high pure nitrogen displacement three times, after tested in the reactor oxygen level after below the 1ppm, vacuumize, in reactor, add 50g sulfonic acid fluoride side group alkene ether monomer (1) (F by the liquid feeding valve
2C=CF-O-CF
2-CF
2-SO
2F) and 60g sulfonic acid fluoride side group alkene ether monomer (2) (F
2C=CF-O-CF
2-CF
2-CF
2CF
2-SO
2F) and 40g cyano group side group alkene ether monomer (F
2C=CF-O-CF
2CF
2-CN) after, filling tetrafluoroethylene monomer to pressure in reactor is 3.9MPa, be warming up to 80 ℃, in reactor, add the 5.2g ammonium persulfate initiator, stopped reaction behind 3.9MPa polymerization 2hr keep-ups pressure, obtain the white polymer powder behind the breakdown of emulsion, after the washing drying, the white polymer powder is dissolved in the solution that is mixed with 10mg/ml concentration in the DMF solvent, carry out the GPC test, the result show number-average molecular weight 22.5 ten thousand, weight-average molecular weight is 360,000, do not detect unusual vibration absorption peak among the infrared test result.
Take above same condition, unique change be in reactor, to add 145g sulfonic acid fluoride side group alkene ether monomer (1) (F by the liquid feeding valve
2C=CF-O-CF
2-CF
2-SO
2F), the concentration and the above term harmonization of total two keys in the guarantee system, the powder of resulting polymers be dissolved in measure GPC result demonstrate number-average molecular weight 12.3 ten thousand, weight-average molecular weight is 20.5 ten thousand, and detected among the infrared test result-the single bonded antisymmetric stretching vibration absorption peak of S-O-C-, appeared at 830cm
-1The place.These results show that short side group cyclisation can occur really in polymerization process, because the interaction of other alkene ether monomers, cyclization can weaken or eliminate.
Claims (10)
1. high-exchange-capacity perfluorinated resin, its short side group sulfonic acid fluoride alkene ether monomer by tetrafluoroethylene, two kinds of different structures, a kind of cyano group side group alkene ether monomer multi-component copolymer close and form, and this resin mainly contains with the repeating unit shown in the following formula (I):
The wherein integer of n=0-3, preferably n=0; The integer of m=2-4; The integer of a, b, c=3-15, the integer of a ', b ', c '=1-3; X/ (x+y+z)=0.2-0.7, y/ (x+y+z)=0.2-0.79, z/ (x+y+z)=0.01-0.1.
2. high-exchange-capacity perfluorinated resin according to claim 1 is characterized in that, the structural formula of the short side group sulfonic acid fluoride alkene ether monomer of described two kinds of different structures is respectively:
The structural formula of described cyano group side group alkene ether monomer is:
The wherein integer of n=0-3, preferably n=0; The integer of m=2-4.
3. high-exchange-capacity perfluorinated resin according to claim 1 and 2, it is characterized in that, the shared molar content percentage ratio of each polymerized unit is in the described resin: the overall molar fraction in tetrafluoroethylene polymerization unit is 50～85%, the overall molar fraction of short side group sulphonyl fluroxene polymerized unit of two kinds of different structures is 5～49%, and the overall molar fraction of cyano group side group alkene ether polymerized unit is 1～10%;
Preferably, the shared molar content percentage ratio of each polymerized unit is in the described resin: the overall molar fraction in tetrafluoroethylene polymerization unit is 70～80%, the overall molar fraction of short side group sulphonyl fluroxene polymerized unit of two kinds of different structures is 15～29%, and the overall molar fraction of cyano group side group alkene ether polymerized unit is 1～5%.
4. according to each described high-exchange-capacity perfluorinated resin of claim 1 to 3, it is characterized in that the mol ratio of the short side group sulphonyl fluroxene polymerized unit (1) of two kinds of different structures and (2) is 0.2-0.8: 0.8-0.2 in the described resin; Be preferably 0.4-0.6: 0.6-0.4.
5. the preparation method of each described high-exchange-capacity perfluorinated resin of claim 1 to 4, this preparation method comprises that the short side group sulfonic acid fluoride alkene ether monomer that makes tetrafluoroethylene, two kinds of different structures, a kind of cyano group side group alkene ether monomer carry out polyreaction under the initiator effect, preferably, the reaction times of described polyreaction is 1～8 hour, temperature of reaction is 10～80 ℃, and reaction pressure is 2～10MPa.
6. preparation method according to claim 5 is characterized in that described initiator is selected from N
2F
2, in perfluoroalkyl superoxide and the persulphate one or more;
Preferably, described perfluoroalkyl superoxide is to be selected from peroxidation perfluoroalkyl acyl compound, peroxidation perfluoro alkoxy acyl compounds, the fluorine-containing alkyl acyl compound of peroxidation part and the peroxidation part fluoroalkoxy acyl compounds one or more; Described persulphate is to be selected from persulfuric acid ammonium salt, basic metal persulfide and the alkaline-earth metal persulfide one or more.
More preferably, described perfluoroalkyl superoxide for be selected from perfluoro propionyl superoxide, 3-chlorine fluorine propionyl superoxide, perfluor methoxyl group acetyl pexoxide,
-H-perfluor butyryl superoxide,
-SO
2F-perfluor-2,5,8-trimethylammonium-3,6,9-trioxa-undecyl superoxide, CF
3CF
2CF
2CO-OO-COCF
2CF
2CF
3, CF
3CF
2CF
2OCFCF
3CO-OO-COCFCF
3OCF
2CF
2CF, CF
3CF
2CH
2CO-OO-COCH
2CF
2CF
3And CF
3OCF
2CF
2CO-OO-COCF
2CF
2OCF
3In one or more; Described persulphate is to be selected from ammonium persulphate and the Potassium Persulphate one or more.
7. according to claim 5 or 6 described preparation methods, it is characterized in that described preparation method also is included in the step that aqueous phase carries out emulsion polymerization;
Preferably, in the emulsion polymerization step, emulsifying agent is selected from anionic emulsifier, for example sodium soap, sodium lauryl sulphate, alkyl sodium sulfonate and sodium alkylarysulfonate; And nonionic emulsifier, alkyl phenol polyether alcohols for example is as in polyoxyethylene nonylphenol ether, polyoxyethylene fatty acid and the polyoxyethylene fatty acid ether one or more;
More preferably, in the emulsion polymerization step, the mass percent concentration of emulsifying agent in water is 0.1-20%, the mass percent concentration of short side group sulfonic acid fluoride alkene ether monomer in water of two kinds of different structures is 5-30%, and the mass percent concentration of cyano group side group alkene ether monomer in water is 1～12%.
8. ion-exchange membrane that is prepared from by each described high-exchange-capacity perfluorinated resin of claim 1 to 4.
9. a fuel cell or electrolytic cell device that comprises the described ion-exchange membrane of claim 8; Described fuel cell is preferably proton membrane fuel battery or high-temperature fuel cell, more preferably the high temperature proton membrane fuel battery; Described electrolyzer is preferably chlor-alkali electrolysis cell.
10. each described high-exchange-capacity perfluorinated resin of claim 1 to 4 is used to make the purposes of fuel cell or electrolytic cell device intermediate ion exchange membrane; Described fuel cell is preferably proton membrane fuel battery or high-temperature fuel cell, more preferably the high temperature proton membrane fuel battery; Described electrolyzer is preferably chlor-alkali electrolysis cell; Preferably, before the use, earlier that the cyano group side group is crosslinked by the chemical process cyclisation.
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| WO2011072417A1 (en) * | 2009-12-15 | 2011-06-23 | 山东东岳神舟新材料有限公司 | High exchange capacity perfluorinated resin, preparation method and use thereof |
| CN106977640A (en) * | 2017-04-18 | 2017-07-25 | 浙江汉丞科技有限公司 | A kind of fluorine-containing chloride conducting polymer one side filled composite film and preparation method thereof |
| US11136424B2 (en) | 2017-04-18 | 2021-10-05 | Zhejiang Hyproof Technology Co., Ltd. | Preparation method for fluorine- and chlorine-containing conductive polymer resin and single- or double-sided filled composite thin film prepared using same and the preparation method therefor |
| CN113861327A (en) * | 2021-09-10 | 2021-12-31 | 广州市乐基智能科技有限公司 | Perfluorosulfonic acid resin binder with high proton conductivity and mechanical properties and preparation method thereof |
| CN115991824A (en) * | 2021-10-18 | 2023-04-21 | 山东东岳未来氢能材料股份有限公司 | Proton exchange membrane containing annular structural unit and preparation method thereof |
| CN117964522A (en) * | 2024-03-29 | 2024-05-03 | 山东东岳未来氢能材料股份有限公司 | Method and device for recovering perfluoro 3, 6-dioxa-4-methyl-7-octenesulfonyl fluoride monomer in polymer |
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| WO2011072417A1 (en) * | 2009-12-15 | 2011-06-23 | 山东东岳神舟新材料有限公司 | High exchange capacity perfluorinated resin, preparation method and use thereof |
| CN106977640A (en) * | 2017-04-18 | 2017-07-25 | 浙江汉丞科技有限公司 | A kind of fluorine-containing chloride conducting polymer one side filled composite film and preparation method thereof |
| US11136424B2 (en) | 2017-04-18 | 2021-10-05 | Zhejiang Hyproof Technology Co., Ltd. | Preparation method for fluorine- and chlorine-containing conductive polymer resin and single- or double-sided filled composite thin film prepared using same and the preparation method therefor |
| CN113861327A (en) * | 2021-09-10 | 2021-12-31 | 广州市乐基智能科技有限公司 | Perfluorosulfonic acid resin binder with high proton conductivity and mechanical properties and preparation method thereof |
| CN113861327B (en) * | 2021-09-10 | 2023-09-26 | 广州市乐基智能科技有限公司 | Perfluorinated sulfonic acid resin binder with high proton conductivity and mechanical property and preparation method thereof |
| CN115991825A (en) * | 2021-10-18 | 2023-04-21 | 山东东岳未来氢能材料股份有限公司 | Fluorine-containing ionic membrane and preparation method thereof |
| CN115991826A (en) * | 2021-10-18 | 2023-04-21 | 山东东岳未来氢能材料股份有限公司 | Perfluorinated phosphonic acid ion exchange membrane and preparation method thereof |
| CN115991824A (en) * | 2021-10-18 | 2023-04-21 | 山东东岳未来氢能材料股份有限公司 | Proton exchange membrane containing annular structural unit and preparation method thereof |
| CN115991824B (en) * | 2021-10-18 | 2023-12-22 | 山东东岳未来氢能材料股份有限公司 | Proton exchange membrane containing annular structural unit and preparation method thereof |
| CN115991825B (en) * | 2021-10-18 | 2023-12-22 | 山东东岳未来氢能材料股份有限公司 | Fluorine-containing ionic membrane and preparation method thereof |
| CN115991826B (en) * | 2021-10-18 | 2023-12-22 | 山东东岳未来氢能材料股份有限公司 | Perfluorinated phosphonic acid ion exchange membrane and preparation method thereof |
| CN117964522A (en) * | 2024-03-29 | 2024-05-03 | 山东东岳未来氢能材料股份有限公司 | Method and device for recovering perfluoro 3, 6-dioxa-4-methyl-7-octenesulfonyl fluoride monomer in polymer |
| CN117964522B (en) * | 2024-03-29 | 2024-06-07 | 山东东岳未来氢能材料股份有限公司 | Method and device for recovering perfluoro 3, 6-dioxa-4-methyl-7-octenesulfonyl fluoride monomer in polymer |
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Address after: 256401 Dongyue fluorosilicone Material Industrial Park, Tangshan Town, Huantai, Zibo, Shandong Patentee after: Shandong Dongyue future hydrogen energy materials Co., Ltd Address before: 256401 Dongyue fluorosilicone Material Industrial Park, Tangshan Town, Huantai, Zibo, Shandong Patentee before: Shandong Dongyue future hydrogen energy materials Co.,Ltd. |
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