CN102731764B - Preparation method of double-metal cyanidation complex catalyst - Google Patents
Preparation method of double-metal cyanidation complex catalyst Download PDFInfo
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- 229910052751 metal Inorganic materials 0.000 title claims abstract description 64
- 239000002184 metal Substances 0.000 title claims abstract description 64
- 239000003054 catalyst Substances 0.000 title claims abstract description 62
- 238000002360 preparation method Methods 0.000 title abstract description 26
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims abstract description 45
- 239000013110 organic ligand Substances 0.000 claims abstract description 23
- 238000000034 method Methods 0.000 claims abstract description 22
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 21
- 150000003983 crown ethers Chemical class 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229920000570 polyether Polymers 0.000 claims abstract description 12
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 10
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000005119 centrifugation Methods 0.000 claims abstract description 9
- 239000002244 precipitate Substances 0.000 claims abstract description 9
- 239000007788 liquid Substances 0.000 claims abstract description 5
- 239000012266 salt solution Substances 0.000 claims abstract description 5
- 239000007864 aqueous solution Substances 0.000 claims abstract description 3
- 238000001556 precipitation Methods 0.000 claims description 18
- 238000007334 copolymerization reaction Methods 0.000 claims description 9
- 239000004417 polycarbonate Substances 0.000 claims description 9
- 229920000515 polycarbonate Polymers 0.000 claims description 9
- 238000003756 stirring Methods 0.000 claims description 9
- 229920005862 polyol Polymers 0.000 claims description 8
- 150000003077 polyols Chemical class 0.000 claims description 8
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 7
- 238000006555 catalytic reaction Methods 0.000 claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 7
- 238000009991 scouring Methods 0.000 claims description 7
- 150000002825 nitriles Chemical class 0.000 claims description 6
- 239000011701 zinc Substances 0.000 claims description 6
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 6
- 238000013019 agitation Methods 0.000 claims description 5
- LGRDAQPMSDIUQJ-UHFFFAOYSA-N tripotassium;cobalt(3+);hexacyanide Chemical compound [K+].[K+].[K+].[Co+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] LGRDAQPMSDIUQJ-UHFFFAOYSA-N 0.000 claims description 5
- ZMARGGQEAJXRFP-UHFFFAOYSA-N 1-hydroxypropan-2-yl 2-methylprop-2-enoate Chemical compound OCC(C)OC(=O)C(C)=C ZMARGGQEAJXRFP-UHFFFAOYSA-N 0.000 claims description 4
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims description 4
- 125000005605 benzo group Chemical group 0.000 claims description 4
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 4
- 229910021645 metal ion Inorganic materials 0.000 claims description 4
- 239000002002 slurry Substances 0.000 claims description 4
- 229910001428 transition metal ion Inorganic materials 0.000 claims description 4
- 238000006735 epoxidation reaction Methods 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 235000005074 zinc chloride Nutrition 0.000 claims description 3
- 239000011592 zinc chloride Substances 0.000 claims description 3
- 229960003280 cupric chloride Drugs 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- BYGOPQKDHGXNCD-UHFFFAOYSA-N tripotassium;iron(3+);hexacyanide Chemical compound [K+].[K+].[K+].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] BYGOPQKDHGXNCD-UHFFFAOYSA-N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 abstract description 21
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 229920000642 polymer Polymers 0.000 abstract description 3
- 238000005406 washing Methods 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 2
- 238000004537 pulping Methods 0.000 abstract 2
- 239000003446 ligand Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 9
- 239000006227 byproduct Substances 0.000 description 6
- 235000011089 carbon dioxide Nutrition 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000010792 warming Methods 0.000 description 5
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 229910001414 potassium ion Inorganic materials 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 159000000021 acetate salts Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000536 complexating effect Effects 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 150000004032 porphyrins Chemical class 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229920001030 Polyethylene Glycol 4000 Polymers 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000005676 cyclic carbonates Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
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- 238000010189 synthetic method Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
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Abstract
The invention discloses a preparation method of a double-metal cyanidation complex catalyst. The method comprises the steps that: a metal cyanide aqueous solution is added into a metal salt solution; crown ether is added and a reaction is carried out; an obtained precipitate is separated by centrifugation; the precipitate is grinded, an organic ligand/water mixed liquid is used for pulping and washing the precipitate; a precipitate is then obtained by centrifugation; puling washing and centrifugation are repeated once or twice; an organic ligand is added into an obtained precipitate for pulping, and a precipitate is separated by centrifugation again; the precipitate is dried, such that the double-metal cyanidation complex catalyst is obtained. With the preparation method provided by the invention, a preparation period is substantially reduced; dosages of the metal salt and the ligand are greatly reduced; and the cost is reduced. The catalytic efficiency of the double-metal cyanidation complex catalyst provided by the invention is equal to a double-metal cyanidation complex catalyst prepared by prior art, but is higher than a catalyst which is not prepared by using crown ether under same conditions. The carbonate bond content of a polymer obtained under the catalytic effect of the double-metal cyanidation complex catalyst provided by the invention is higher than that of the catalyst which is not prepared by using crown ether. Also, the high catalytic performance of the catalyst provided by the invention make the catalyst suitable for the productions of polyether glycol.
Description
Technical field
The present invention relates to a kind of method of preparing double metal cyanide catalyst (DMC).
Background technology
The catalyst system of can catalyzed copolymerization preparing polycarbonate polyol of finding at present has: metal acetate salt (K.Soga et al, Makromol.Chem., 1978,179,2837), porphyrin aluminium catalyst system (S.Inoue ct al., Macromol., 1986.19,8) and polymer-supported bimetal complex (Chen Liban, CN 1032010C) etc., but these systems all exist a lot of shortcomings, the catalysis productive rate of metal acetate salt is lower.The cost of porphyrin Al catalysts is high, is not suitable for suitability for industrialized production.The carbonic acid ester bond content of polymer-supported Bimetallic catalyst system catalysate is generally lower than 30%, and lower carbonic acid ester bond content makes it more approach polyethers but not polycarbonate.
Since the eighties in last century, people are used for catalysis epoxidation thing and carbon dioxide copolymerization by double metal cyanide catalyst, as US Patent No. 4500704.The synthetic method of this catalyzer has relevant open introduction in the patents such as JP4145123, US5470813, EP700949, WO97/40086 and CN1255074.By improving preparation method, this catalyzer is catalysis carbonic acid gas and the highest catalyst system of epoxide copolymerization catalytic efficiency so far, and it is insensitive to moisture and oxygen, less demanding to environment.Wherein Zhejiang University old upper (polymer, 2004,45,6519-6524) synthetic catalyzer, more than catalytic efficiency can reach 2000g/g.Zhou Tongchang (Journal of polymer research, 2011,18,6, more than the catalytic efficiency of the bimetallic catalyst of 2071-2076) preparing reaches as high as 7000g/g.These researchs, make bimetal complex become the catalyzer that carbon dioxide copolymerization field has industrial prospect most above.
The sixties in 20th century, AM General rubber company utilized double metal cyanide catalyst catalysis homopolymerization to prepare polyether glycol (US3829505) first, the alkali formula preparation method who compares traditional, the method has outstanding advantages, as narrow in the molecular weight distribution of: polyethers, degree of unsaturation is low, by product is few etc.Therefore, since the eighties in 20th century, there is a large amount of research for polyether glycol aspect about double metal cyanide catalyst, as: US3404109, US3900518, US4239879, US4242490, US4355188, US 4985491, US5032671, US5158922, US5627120, US7034103, US7169956 etc.Wherein in the nineties in 20th century, the successfully production for polyether glycol by bimetal complex catalyst of US4843054, and US5789626 makes to utilize, and bimetallic catalyst prepares polyether glycol more has a commercial promise.
In existing bimetal complex catalyst preparation method, the solution washing several that contains organic ligand and water for the throw out that metal-salt and prussiate reaction generate, and by centrifuging or filtration method, filter dry the grinding of precipitation finally obtaining.This preparation method's process is loaded down with trivial details, and preparation cycle is long, easily introduces unstable factor.Owing to having used in a large number metal-salt and organic ligand in preparation process, make cost also higher simultaneously.Preparation method to catalyzer improves, and is guaranteeing that catalyzer has under the prerequisite of high catalytic efficiency, simplifies technique, shortens preparation cycle, reduces costs and just seems particularly important.
Summary of the invention
In order to overcome the shortcoming and deficiency of prior art, the object of the present invention is to provide a kind of method of preparing double metal cyanide catalyst, the preparation cycle of the method is only the 1/3 even shorter of prior art, the consumption of metal-salt is only 1/10 of prior art, organic ligand consumption be only prior art 1/3 even still less, and simplified widely the technological process of production, reduced cost.
Object of the present invention is achieved through the following technical solutions:
A method of preparing double metal cyanide catalyst, comprises the following steps:
(1) under vigorous stirring, the metal cyanides aqueous solution is slowly joined in metal salt solution, then add crown ether, continue vigorous stirring 1-5h, centrifugation precipitation;
(2) step (1) gained precipitation is ground, and will precipitation plasm scouring with organic ligand/water mixed liquid, insulated and stirred 1-5h, then centrifuging and taking precipitates; Repetition plasm scouring and centrifugal 0-2 time; (" repeated centrifugation and change plasm scouring 0 time " represents after precipitation grinding, to enter next step, without changing plasm scouring);
(3) in the precipitation of step (2) gained, add organic ligand to stir 1-3hization slurry, recentrifuge precipitation separation, obtains double metal cyanide catalyst after precipitation is dried;
The described metal cyanides of step (1) is water soluble metal cyanide, preferably the Tripotassium iron hexacyanide or potassium cobalticyanide;
The described metal-salt of step (1) is a kind of in zinc chloride, iron protochloride, cupric chloride or iron(ic) chloride;
The solvent of the described metal salt solution of step (1) is water and organic ligand;
The metal-salt that step (1) is described and the mol ratio of metal cyanides are (1-4): 1;
The described crown ether of step (1) is a kind of in hexaoxacyclooctadecane-6-6, benzo hexaoxacyclooctadecane-6-6 or dibenzo hexaoxacyclooctadecane-6-6;
In organic ligand/water mixed liquid described in step (2), the volume ratio of organic ligand and water is 1: 1;
The described organic ligand of step (2) is a kind of in the trimethyl carbinol, glycol dimethyl ether, vinylformic acid hydroxy butyl ester or Rocryl 410;
Described dry of step (3) is dry 4-15h at 40-70 ℃.
The double metal cyanide catalyst being prepared by aforesaid method has as follows and forms: M
iI 3[M
iII(CN)
6]
2aM
iIx
2bLcH
2odCR, wherein, M
iIfor divalent-metal ion, M
iIIfor transition metal ion, X is halogen, and L is organic ligand, and CR is crown ether, and a, b, c, d are respectively M
iIx
2, L, H
2the relative quantity of O, CR, a, b, c, d are 1-10;
The preferred Zn of described divalent-metal ion
2+, Fe
2+, Ni
2+or Co
2+; The preferred Co of described transition metal ion
2+, Co
3+, Fe
2+or Fe
3+; Described organic ligand is the trimethyl carbinol, glycol dimethyl ether, vinylformic acid hydroxy butyl ester or Rocryl 410; Described crown ether is hexaoxacyclooctadecane-6-6, benzo hexaoxacyclooctadecane-6-6 or dibenzo hexaoxacyclooctadecane-6-6.
Its particle diameter of described double metal cyanide catalyst reaches 10
-7m rank.
The double metal cyanide catalyst being prepared by aforesaid method can be used for catalyzed copolymerization reaction and obtains polycarbonate polyol, also can be used for catalysis epoxidation thing generation homopolymerization and generates polyether glycol.
Principle of the present invention is: existing double metal cyanide catalyst is in preparation process, in order to remove the potassium ion that affects catalytic efficiency, to have used a large amount of metal-salts and changed plasm scouring process, this preparation method's process is loaded down with trivial details, preparation cycle is long, easily introduces unstable factor.Owing to having used in a large number metal-salt and organic ligand in preparation process, make cost also higher simultaneously.And the crown ether of hexaoxacyclooctadecane-6-6 class and the radius of potassium ion just in time meet, potassium ion is had to extraordinary complexing action, so in preparation method of the present invention, carry out complexing potassium ion with crown ether in washingization slurry process.The catalytic efficiency of double metal cyanide catalyst of the present invention in catalyzed copolymerization, between (3-6) * 1000g/g, guaranteeing, under the prerequisite of high catalytic activity, to have improved preparation technology.
The present invention has following advantage and effect with respect to prior art:
1, the preparation method of double metal cyanide catalyst of the present invention has shortened preparation cycle greatly, and preparation process is simplified, and is not subject to the interference of extraneous factor.
2, in the preparation method of double metal cyanide catalyst of the present invention, the consumption of metal-salt and organic ligand greatly reduces, and has reduced cost.
3, its catalytic efficiency of double metal cyanide catalyst of the present invention and existing method prepare double metal cyanide catalyst maintain an equal level (catalytic efficiency is high), and can control copolyreaction by-products content and be low to moderate 3-5%.
4, its catalytic efficiency of double metal cyanide catalyst of the present invention will be higher than under equal conditions but the catalyzer that does not add crown ether to prepare, and its carbonic acid ester bond content of the polymkeric substance being obtained by the former catalysis also will be higher than the latter.
Accompanying drawing explanation
Fig. 1 is the infrared spectrogram of embodiment 1 resulting double metal cyanide catalyst.
Fig. 2 is the infrared spectrogram of embodiment 2 resulting double metal cyanide catalysts.
Embodiment
Below in conjunction with embodiment and accompanying drawing, the present invention is described in further detail, but embodiments of the present invention are not limited to this.
Embodiment 1
, by following steps, prepared:
(1) 0.01mol potassium cobalticyanide is dissolved in 50mL water and obtains potassium cobalticyanide solution, 0.037mol zinc chloride is dissolved in the mixed solution of 150mL water and the 75mL trimethyl carbinol and obtains liquor zinci chloridi; Under vigorous stirring, potassium cobalticyanide solution is slowly splashed in liquor zinci chloridi, 30min drips off, and then adds 0.03mol hexaoxacyclooctadecane-6-6, continues vigorous stirring 5h;
(2) centrifugation precipitation, gained is deposited in grinding in ball grinder and uses the mixed liquefied slurry of the 125mL trimethyl carbinol and 125mL water, stirs insulation 1h; After centrifugal, again with the mixed solution of the 125mL trimethyl carbinol and 125mL water, precipitation is starched, stir insulation 1h;
(3) centrifugal, 1h is starched and stirred to precipitation by the pure trimethyl carbinolization, centrifugation precipitation; To be deposited in dry 15h in the vacuum drying oven of 45 ℃, obtain the double metal cyanide catalyst of white powder.By ultimate analysis (in Table 1) and infrared spectra (seeing Fig. 1), determine that it consists of Zn
3[Co (CN)
6]
21.7ZnCl
21.4t-BuOH2.2H
2o0.15CR.
The results of elemental analyses of the double metal cyanide catalyst that table 1 embodiment 1 obtains
| Element massfraction (%) | Zn | Co | C | H | N | Cl | O |
| 30.76 | 9.69 | 25.90 | 2.71 | 17.55 | 2.90 | 9.93 |
Embodiment 2
A preparation method for double metal cyanide catalyst, its raw material and operation, with embodiment 1, just from start to finish do not add hexaoxacyclooctadecane-6-6.By ultimate analysis (in Table 2) and infrared spectra (seeing Fig. 2), determine, it consists of Zn the double metal cyanide catalyst finally obtaining
3[Co (CN)
6]
21.6ZnCl
21.1t-BuOH1.8H
2o.
The results of elemental analyses of the double metal cyanide catalyst that table 2 embodiment 2 obtains
| Element massfraction (%) | Zn | Co | C | H | N | Cl | O |
| 31.25 | 9.96 | 25.50 | 2.51 | 17.42 | 2.89 | 9.92 |
Embodiment 3
Under nitrogen protection, in the 130ml autoclave being fully dried, add 7mg embodiment 1 gained catalyzer, 24.9g propylene oxide, is filled with carbonic acid gas 18g, is warming up to 80 ℃.Under agitation condition, react 15h and emit product, vacuum is removed unreacted propylene oxide, obtains polycarbonate polyol 28.7g, and test result shows that in product, carbonic acid ester bond content is 44%, and by product (cyclic carbonate) content is 3%.The about 4100g/g of catalytic efficiency.
Under nitrogen protection, in the 130ml autoclave being fully dried, add 7mg embodiment 2 gained catalyzer, then add 24.9g propylene oxide, be filled with carbonic acid gas 18g, be warming up to 80 ℃.Under agitation condition, react 15h and emit product, vacuum is removed unreacted propylene oxide, obtains the polycarbonate polyol 26.8g that viscosity is very high, and test result shows that in product, carbonic acid ester bond content is 35%, and by-products content is 2%.The about 3838g/g of catalytic efficiency.
From above-mentioned experimental result, can find out, catalyzed copolymerization at 80 ℃, the double metal cyanide catalyst that in its catalytic efficiency of the resulting double metal cyanide catalyst of embodiment 1 and the polycarbonate polyol that obtains, the content of carbonic acid ester bond all obtains apparently higher than embodiment 2.Illustrate that adding the character impact of double metal cyanide catalyst of crown ether is very large.
Embodiment 4
Under nitrogen protection, in the 130ml autoclave being fully dried, add 7mg embodiment 1 gained catalyzer, 24.9g propylene oxide, is filled with carbonic acid gas 18g, is warming up to 70 ℃.Under agitation condition, react 38h and emit product, vacuum is removed unreacted propylene oxide, obtains polycarbonate polyol 33.5g, and test result shows that in product, carbonic acid ester bond content is 57%, and by-products content is 3%.The about 4785g/g of catalytic efficiency.
Under nitrogen protection, in the 130ml autoclave being fully dried, add 7mg embodiment 2 gained catalyzer, then add 24.9g propylene oxide, be filled with carbonic acid gas 18g, be warming up to 70 ℃.Under agitation condition, react 38h and emit product, vacuum is removed unreacted propylene oxide, the polycarbonate polyol 22.3g obtaining, and test result shows that in product, carbonic acid ester bond content is 32%, by-products content is 2%.The about 3179g/g of catalytic efficiency.
From above-mentioned experimental result, can find out, catalyzed copolymerization at 70 ℃, add crown ether (being the double metal cyanide catalyst of embodiment 1) than the catalyzer that does not add crown ether (being the double metal cyanide catalyst of embodiment 2) to prepare, in its catalytic efficiency and product, carbonic acid ester bond content is all higher, and adding the character impact of double metal cyanide catalyst of crown ether is very large.
Embodiment 5
In 1000ml reactor, add bimetallic catalyst, the 10g PEG-4000 of preparation in 10mg embodiment 1 to be warming up to 115 ℃, vacuum nitrogen gas three times; Add 21g propylene oxide, observe after pressure drop, then add 415g propylene oxide, be reacted to pressure and no longer decline, emit product, unreacted monomer volatilization is clean, obtain polyether glycol 353g, molecular weight is 8500, the about 35.3kg/g of catalytic efficiency, the about 3.2mmol/kg of degree of unsaturation.
Can find out, double metal cyanide catalyst prepared by the inventive method also can be used for the homopolymerization of epoxy compounds, prepares polyether glycol, and its catalytic efficiency is higher.Simplify the preparation technology of double metal cyanide catalyst, also expanded the application prospect of this catalyzer on polyether glycol is produced.
Above-described embodiment is preferably embodiment of the present invention; but embodiments of the present invention are not restricted to the described embodiments; other any do not deviate from change, the modification done under spirit of the present invention and principle, substitutes, combination, simplify; all should be equivalent substitute mode, within being included in protection scope of the present invention.
Claims (8)
1. a method of preparing double metal cyanide catalyst, is characterized in that comprising the following steps:
(1) under agitation, the metal cyanides aqueous solution is joined in metal salt solution, then add crown ether, continue to stir 1-5h, centrifugation precipitation;
(2) step (1) gained precipitation is ground, and will precipitation plasm scouring with organic ligand/water mixed liquid, insulated and stirred 1-5h, then centrifuging and taking precipitates; Repetition plasm scouring and centrifugal 0-2 time;
(3) in the precipitation of step (2) gained, add organic ligand to stir 1-3hization slurry, recentrifuge precipitation separation, obtains double metal cyanide catalyst after precipitation is dried;
The described metal cyanides of step (1) is the Tripotassium iron hexacyanide or potassium cobalticyanide;
The described metal-salt of step (1) is a kind of in zinc chloride, iron protochloride or cupric chloride;
The described crown ether of step (1) is a kind of in hexaoxacyclooctadecane-6-6, benzo hexaoxacyclooctadecane-6-6 or dibenzo hexaoxacyclooctadecane-6-6;
The described organic ligand in step (2) and (3) is a kind of in the trimethyl carbinol, glycol dimethyl ether, vinylformic acid hydroxy butyl ester or Rocryl 410.
2. the method for preparing double metal cyanide catalyst according to claim 1, is characterized in that: the solvent of the described metal salt solution of step (1) is water and organic ligand.
3. the method for preparing double metal cyanide catalyst according to claim 1, is characterized in that: the metal-salt that step (1) is described and the mol ratio of metal cyanides are (1-4): 1.
4. the method for preparing double metal cyanide catalyst according to claim 1, is characterized in that: in the organic ligand/water mixed liquid described in step (2), the volume ratio of organic ligand and water is 1:1.
5. the double metal cyanide catalyst that described in claim 1-4 any one, method prepares, is characterized in that: have following composition: M
iI 3[M
iII(CN)
6]
2aM
iIx
2bLcH
2odCR;
Wherein, M
iIfor divalent-metal ion, M
iIIfor transition metal ion, X is halogen, and L is organic ligand, and CR is crown ether, and a, b, c, d are respectively M
iIx
2, L, H
2the relative quantity of O, CR, a, b, c, d are 1-10.
6. double metal cyanide catalyst according to claim 5, is characterized in that: described divalent-metal ion is Zn
2+, Fe
2+or Cu
2+; Described transition metal ion is Co
3+or Fe
3+; Described organic ligand is the trimethyl carbinol, glycol dimethyl ether, vinylformic acid hydroxy butyl ester or Rocryl 410; Described crown ether is hexaoxacyclooctadecane-6-6, benzo hexaoxacyclooctadecane-6-6 or dibenzo hexaoxacyclooctadecane-6-6.
7. the double metal cyanide catalyst described in claim 5 or 6 generates the application in polycarbonate polyol in catalyzed copolymerization reaction.
8. the double metal cyanide catalyst described in claim 5 or 6 generates the application in polyether glycol at catalysis epoxidation thing generation homopolymerization.
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|---|---|---|---|
| CN201210106977.2A CN102731764B (en) | 2012-04-12 | 2012-04-12 | Preparation method of double-metal cyanidation complex catalyst |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210106977.2A CN102731764B (en) | 2012-04-12 | 2012-04-12 | Preparation method of double-metal cyanidation complex catalyst |
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| US5789626A (en) * | 1996-04-19 | 1998-08-04 | Arco Chemical Technology, L.P. | Highly active double metal cyanide catalysts |
| CN101003622A (en) * | 2007-01-18 | 2007-07-25 | 浙江大学 | Catalyst of load type bimetallic cyaniding complex, preparation method and application |
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| US5789626A (en) * | 1996-04-19 | 1998-08-04 | Arco Chemical Technology, L.P. | Highly active double metal cyanide catalysts |
| CN101003622A (en) * | 2007-01-18 | 2007-07-25 | 浙江大学 | Catalyst of load type bimetallic cyaniding complex, preparation method and application |
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