CN1544483A - PTMEG polymerization catalyst preparation method - Google Patents
PTMEG polymerization catalyst preparation method Download PDFInfo
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- CN1544483A CN1544483A CNA2003101153970A CN200310115397A CN1544483A CN 1544483 A CN1544483 A CN 1544483A CN A2003101153970 A CNA2003101153970 A CN A2003101153970A CN 200310115397 A CN200310115397 A CN 200310115397A CN 1544483 A CN1544483 A CN 1544483A
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- acid
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- ptmeg
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- 229920000909 polytetrahydrofuran Polymers 0.000 title claims abstract description 17
- 238000002360 preparation method Methods 0.000 title claims description 16
- 239000002685 polymerization catalyst Substances 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract description 27
- BCTWNMTZAXVEJL-UHFFFAOYSA-N phosphane;tungsten;tetracontahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.P.[W].[W].[W].[W].[W].[W].[W].[W].[W].[W].[W].[W] BCTWNMTZAXVEJL-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000013078 crystal Substances 0.000 claims abstract description 25
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000002253 acid Substances 0.000 claims abstract description 16
- 239000003377 acid catalyst Substances 0.000 claims abstract description 12
- CMPGARWFYBADJI-UHFFFAOYSA-L tungstic acid Chemical compound O[W](O)(=O)=O CMPGARWFYBADJI-UHFFFAOYSA-L 0.000 claims abstract description 12
- 238000001816 cooling Methods 0.000 claims abstract description 10
- 238000005406 washing Methods 0.000 claims abstract description 10
- 238000006243 chemical reaction Methods 0.000 claims abstract description 9
- XMVONEAAOPAGAO-UHFFFAOYSA-N sodium tungstate Chemical compound [Na+].[Na+].[O-][W]([O-])(=O)=O XMVONEAAOPAGAO-UHFFFAOYSA-N 0.000 claims abstract description 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000002425 crystallisation Methods 0.000 claims abstract description 6
- 239000008139 complexing agent Substances 0.000 claims abstract description 3
- 239000007864 aqueous solution Substances 0.000 claims description 15
- 239000000243 solution Substances 0.000 claims description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 8
- 239000012065 filter cake Substances 0.000 claims description 8
- -1 HPA ether adducts Chemical class 0.000 claims description 7
- 150000002170 ethers Chemical class 0.000 claims description 7
- 238000003756 stirring Methods 0.000 claims description 6
- 229910019142 PO4 Inorganic materials 0.000 claims description 5
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- 238000009835 boiling Methods 0.000 claims description 5
- 238000005119 centrifugation Methods 0.000 claims description 5
- 239000008367 deionised water Substances 0.000 claims description 5
- 229910021641 deionized water Inorganic materials 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 5
- 229910052742 iron Inorganic materials 0.000 claims description 5
- 239000012452 mother liquor Substances 0.000 claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 5
- 239000010452 phosphate Substances 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- 229910001415 sodium ion Inorganic materials 0.000 claims description 5
- 238000010792 warming Methods 0.000 claims description 5
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- VUEDNLCYHKSELL-UHFFFAOYSA-N arsonium Chemical compound [AsH4+] VUEDNLCYHKSELL-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 238000004090 dissolution Methods 0.000 claims description 2
- 229910001385 heavy metal Inorganic materials 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 238000012544 monitoring process Methods 0.000 claims description 2
- 238000005057 refrigeration Methods 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 7
- 238000006116 polymerization reaction Methods 0.000 abstract description 6
- 239000003054 catalyst Substances 0.000 abstract description 5
- 238000010438 heat treatment Methods 0.000 abstract description 5
- 238000000926 separation method Methods 0.000 abstract description 4
- 238000000605 extraction Methods 0.000 abstract description 2
- 239000007788 liquid Substances 0.000 abstract 2
- 230000008025 crystallization Effects 0.000 abstract 1
- 230000003028 elevating effect Effects 0.000 abstract 1
- 238000004321 preservation Methods 0.000 abstract 1
- 229910052721 tungsten Inorganic materials 0.000 abstract 1
- 239000010937 tungsten Substances 0.000 abstract 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 7
- 238000001914 filtration Methods 0.000 description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 4
- 239000011964 heteropoly acid Substances 0.000 description 4
- 230000036571 hydration Effects 0.000 description 4
- 238000006703 hydration reaction Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000005303 weighing Methods 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 230000000740 bleeding effect Effects 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- AVFBYUADVDVJQL-UHFFFAOYSA-N phosphoric acid;trioxotungsten;hydrate Chemical compound O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.OP(O)(O)=O AVFBYUADVDVJQL-UHFFFAOYSA-N 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical group CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 102000004160 Phosphoric Monoester Hydrolases Human genes 0.000 description 1
- 108090000608 Phosphoric Monoester Hydrolases Proteins 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- 238000007171 acid catalysis Methods 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000006900 dealkylation reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000000909 electrodialysis Methods 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 150000001457 metallic cations Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002468 redox effect Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- PBYZMCDFOULPGH-UHFFFAOYSA-N tungstate Chemical compound [O-][W]([O-])(=O)=O PBYZMCDFOULPGH-UHFFFAOYSA-N 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
The invention relates to a process for preparing 12-tungstophosphoric acid catalyst for PTMEG polymerization comprising the steps in sequence, (1) dissolving sodium tungstate crystal of industrial grade into water, and charging hydrogen dioxide complexing agent, cooling down, (2) heat preservation, filling definite quantity of dilute hydrochloric acid, (3) letting in SO2 slowly, washing with dilute hydrochloric acid and water after reaction, (4) charging the prepared active tungstic acid with rather high purity immediately into phosphoric water solution, agitating, elevating temperature, condensing, controlling process end spot according to weight, the invention is characterized in that the process also comprises, (5) subjecting the concentration liquid to cooling crystallization, separating mother liquid by centrifugal separation, (6) adding equal volumn of C3-C20 ether to the water solution of the dissolved crystal for extraction to obtain HPA ether addition product, rinsing the ether addition product by the diluted acid of the equal volume, the high purity 12-tungsten phosphoric catalyst is thus obtained through heating and concentrating the ether addition product.
Description
(1) technical field
The present invention relates to the method that a kind of preparation is used for PTMEG polymeric catalyzer.Relate to the method that a kind of preparation is used for PTMEG polymeric 12-tungstophosphoric acid catalyst particularly.
(2) background technology
The 12-tungstophosphoric acid is that a kind of new catalyst causes people's attention day by day; it has acidity and redox property simultaneously; on industrial application, be better than traditional catalyst; can be used for hydration in the organic synthesis field; ester (ester decomposition) is changed; transesterify; decompose; alkylation-dealkylation; the acetate acidolysis; poly-(contracting) closes; the epoxide etherificate; acidylate; isomerization; nitrated etc.; the 12-tungstophosphoric acid is made its catalytic activity height of catalyzer; selectivity is good; pollute little advantage such as easy to control; particularly produce in the PTMEG production and select for use the 12-tungstophosphoric acid to make catalyst system, have more many advantages in the THF polymerization.
So far, the catalytic industrialization project of 12-tungstophosphoric acid has 7 kinds at least, they are: 1, third rare direct hydration is produced Virahol, 2, Methylacrylaldehyde oxidation production methyl-prop diluted acid, 3, the trimethyl carbinol is produced in the iso-butylene hydration, and 4, n-butylene hydration, dehydrogenation produce butanone-2,5, tetrahydrofuran ring opening polymerization produces PTMEG, 6, bisphenol S is produced in phenol and sulfuric acid condensation, and 7, p-cresol and iso-butylene alkylation production antioxidant 264.The application of 12-tungstophosphoric acid catalyst reduces widely or has overcome existing serious environment pollution of traditional technology and etching apparatus problem in these chemical projects, quality product and yield have been improved significantly, have remarkable economic efficiency and social benefit, so the industrial preparation technology of 12-tungstophosphoric acid catalyst has become the heat subject of catalyzer circle research and development.
A kind of method of the 12-of preparation tungstophosphoric acid is disclosed in the English Patent 1311849 (1973) by JOHN NORMAN SANSOM and RAYMOND ANTHONY SMITH invention.This method adds long-time heating behind nitric acid or the hydrochloric acid with stoichiometric calcium wolframate and phosphoric acid, generates 12-tungstophosphoric acid calcium salt, it is separated after vulcanization acid generate calcium sulfate and 12-tungstophosphoric acid.This method step complexity, impurity is many, and yield is low.
By Institute of Photogrophic Chemistry, Academia Sinica application, the Chinese patent 99124994.1 of people such as Zhang Linhua invention discloses a kind of " preparation method of 12-tungstophosphoric acid ", and " this method is raw material with the tungstophosphoric acid, adds the complexing agent hydrogen peroxide, adds mineral acid again.The concentration of the acid of control reaction system adds reductive agent again and obtains active tungstic acid.Above-mentioned active tungstic acid directly is dissolved in the dilute phosphoric acid, obtains 12-tungstophosphoric acid crystal behind the condensing crystal.But the heteropolyacid catalyst that this method is produced contains the sodium ion of 200～500PPM and small amounts of iron, aluminium, chromium, plumbous plasma usually, if these hetero-ions are not removed, will be very big to influences such as the polymerization catalyzed activity of PTMEG, selectivity and PTMEG quality producies.
By the synthetic 12-tungstophosphoric acid method of Russ P RU1559773 (1994) electrodialysis of people such as К у п и к о в а OM invention, the product purity height of production, but industrialization difficulty, and yield less than 30%.
Usually, the 12-tungstophosphoric acid catalyst is to mix with phosphoric acid or sodium phosphate salt with sodium wolframate, removes metallic cation by the strong acid exchange again and makes it to become free 12-tungstophosphoric acid.Add strong acid (hydrochloric acid, sulfuric acid, nitric acid etc.) and transfer PH, use a large amount of extracted with diethyl ether, form the etherate of heteropolyacid, add the aqueous solution that this etherate of water thermal degradation obtains heteropolyacid, condensing crystal gets the heteropolyacid crystal, and this method is used solvent ether in a large number, and yield is not high, and in the industrial sodium wolframate the deleterious impurity of PTMEG polyreaction is taken in the 1 2-tungstophosphoric acid crystal, it is polymerization catalyzed to influence PTMEG.
(3) summary of the invention
The objective of the invention is to overcome the defective of above-mentioned prior art, provide that a kind of flow process is short, method is simple, the method for preparing the 12-tungstophosphoric acid catalyst of low cost of manufacture.
The present invention also aims to provide a kind of method of the highly purified 12-of preparation tungstophosphoric acid catalyst of the PTMEG of can be used for polyreaction, resulting PTMEG product yield height, quality is good.
A kind of preparation of the present invention is used for the method for PTMEG polymeric catalyzer, and order comprises the following steps:
A) will dissolve the aqueous solution that is mixed with 10-30WT% in the technical grade sodium wolframate crystal input water, adding concentration is 30WT% hydrogen peroxide complex thing, and the complex compound add-on is pressed 1.1～1.5 times of sodium wolframate molar weight, stir and be cooled to 3～5 ℃,
B) slowly adding with the sodium wolframate aqueous solution volume ratio is 3～5: 1 18% dilute hydrochloric acid, and whole process maintains the temperature in 3～15 ℃ of scopes,
C) slowly feed SO by gas distributor
2, strict control feeding speed guarantee system temperature is at 5～10 ℃, be reacted to terminal point after, change three sections band filters over to, wash Na in the monitoring washings continuously by 1N, 0.5N, 0.1N dilute hydrochloric acid and deionized water
+% content is less than 5ppm, guarantee sodium ions content in the wolframic acid filter cake less than 100ppm, iron and aluminium composition also all less than the high-purity activity wolframic acid of 10ppm.
G) the high-purity activity wolframic acid with preparation joins in 0.1 ± 0.025mol/L phosphate aqueous solution immediately, the concentration of active tungstic acid is controlled at 1.5 ± 0.25mol/L, fully stirred 2-4 hour, slowly be warming up to 50 ℃～80 ℃ reaction solution clears then, continue the boiling that heats up, continue to be concentrated into terminal point, terminal point is judged by weight.
It is characterized in that also comprising:
H) concentrated solution is put into screw-pushing type refrigeration crystallizer and is carried out crystallisation by cooling, will contain the mother liquor centrifugation of crystal weight 5%～8%,
I) the gained dissolution of crystals is mixed with ether that 50% aqueous solution adds equal-volume C3～C20 extract HPA ether adducts, use isopyknic 0.05%～0.15% Diluted Acid Washing ether adducts again, it is zero high purity 12-tungstophosphoric acid catalysis that ether adducts intensification condensing crystal is obtained sodium ion≤20ppm, iron ion≤5ppm, aluminum ion≤5ppm, arsonium ion≤5ppm, heavy metal content≤2ppm, insoluble in water thing.
Feature of the present invention is: pass through reasonable washing, purifying in the active tungstic acid preparation, once remove various hetero-ions, obtain the high purity wolframic acid, and directly add phosphatase reaction, concentration of reaction solution just can obtain primary 12-tungstophosphoric acid crystal, in a synthetic step of active tungstic acid, strictly optimize the synthetic of active tungstic acid, the polymerization degree of active tungstic acid controlled well [refers to (WO
3.XH
2O) n polymerization number n], n=150+50, best filtration washing in this scope.By the ether extraction, wash the method second removal trace hetero-ion and the abnormally-structured polyacid of adducts, improve the purity of HPA greatly.
Advantage of the present invention:
1, purity height, catalytic activity are stable, selectivity is good, and the PTMEG quality product is excellent.
2, yield height can reach more than 70%.
3, flow process is simple, and is easy to control, and production cost is low.
4, pollution is little, safe.
(4) specific embodiments
Embodiments more of the present invention see following embodiment for details, with the catalyzer of Chinese patent 99124994.1 " preparation method of 12-tungstophosphoric acid " preparation as a comparison case.
Embodiment 1
Take by weighing 509 gram sodium wolframates and join in the container that 5200mL water is housed and dissolve, add 30%H
2O
2Solution 120ml stirs ice bath and cools to 10 ℃, slowly adds the hydrochloric acid 0.75L of 6N, and whole process maintains the temperature in 6～8 ℃ of scopes, slowly feeds SO by gas distributor
2After being reacted to terminal point, with the filtration of bleeding of cloth formula funnel, filter cake is passed through 1N continuously, 0.6N, 0.2N each 4L of dilute hydrochloric acid and 6L deionized water wash, the filter cake of washing and filtering is joined in the 0.13mol/L phosphate aqueous solution immediately, the concentration of active tungstic acid is controlled at 1.15mol/L, fully stirred 2 hours, slowly be warming up to 50 ℃ of reaction solution clears by heating curve then, boiling heats up, continue to be concentrated into terminal point, concentrated solution is put into cooling crystallizer carry out crystallisation by cooling, will contain the 12-tungstophosphoric acid crystal centrifugation of a small amount of mother liquor, the gained crystal is mixed with 50% the aqueous solution, add 180mL ether thorough mixing, leave standstill and take off a layer ether adducts, add 200mL0.5N dilute hydrochloric acid and wash the ether adducts, standing separation is taken off a layer ether adducts and is warmed up to 50 ℃ of condensing crystals, obtain 261.8 gram high purity white 12-tungstophosphoric acid catalysts, yield is 70.8%.
Embodiment 2
Take by weighing 509 gram sodium wolframates and join in the container that 3200mL water is housed and dissolve, add 30%H
2O
2Solution 107ml stirs ice bath and cools to 5 ℃, slowly adds the hydrochloric acid 0.68L of 6N, and whole process maintains the temperature in 4～5 ℃ of scopes, slowly feeds SO by gas distributor
2After being reacted to terminal point, with the filtration of bleeding of cloth formula funnel, filter cake is passed through 1N continuously, 0.5N, 0.1N each 4L of dilute hydrochloric acid and 6.5L deionized water wash, the filter cake of washing and filtering is joined in the 0.12mol/L phosphate aqueous solution immediately, the concentration of active tungstic acid is controlled at 1.15mol/L, fully stirred 2 hours, slowly be warming up to 50 ℃ of reaction solution clears by heating curve then, boiling heats up, continue to be concentrated into terminal point, concentrated solution is put into cooling crystallizer carry out crystallisation by cooling, will contain the 12-tungstophosphoric acid crystal centrifugation of a small amount of mother liquor, the gained crystal is mixed with 70% the aqueous solution, add the 250mL third butyl ether thorough mixing, leave standstill and take off the layer third butyl ether adducts, add 180mL1N dilute hydrochloric acid and wash the third butyl ether adducts, standing separation is taken off the layer third butyl ether adducts and is warmed up to 75 ℃ of condensing crystals, obtain 262.2 gram high purity white 12-tungstophosphoric acid catalysts, yield is 71%.
Embodiment 3
Take by weighing 1000 gram sodium wolframates and join in the container that 7200mL water is housed and dissolve, add 30%H
2O
2Solution 219ml stirs ice bath and cools to 10 ℃, slowly adds the hydrochloric acid 1.6L of 6N, and whole process maintains the temperature in 7～10 ℃ of scopes, slowly feeds SO by gas distributor
2After being reacted to terminal point, with the filtration of bleeding of cloth formula funnel, filter cake is passed through 1N continuously, 0.5N, 0.1N each 10L of dilute hydrochloric acid and 12L deionized water wash, the filter cake of washing and filtering is joined in the 0.12mol/L phosphate aqueous solution immediately, the concentration of active tungstic acid is controlled at 1.14mol/L, fully stirred 3 hours, slowly be warming up to 50 ℃ of reaction solution clears by heating curve then, boiling heats up, continue to be concentrated into terminal point, concentrated solution is put into cooling crystallizer carry out crystallisation by cooling, will contain the 12-tungstophosphoric acid crystal centrifugation of a small amount of mother liquor, the gained crystal is mixed with 30% the aqueous solution, add 400mL propyl ether thorough mixing, leave standstill and take off a layer propyl ether adducts, add 500mL0.1N dilute hydrochloric acid and wash the propyl ether adducts, standing separation is taken off a layer propyl ether adducts and is warmed up to 72 ℃ of condensing crystals, obtain 325.1 gram high purity white 12-tungstophosphoric acid catalysts, yield is 71.5%.
Comparative Examples 1
With Chinese patent 99124994.1 " preparation method of 12-tungstophosphoric acid " preparation, make 12-tungstophosphoric acid catalyst 300g.
Active verification method: at first embodiment 1 sample and Comparative Examples 1 sample are carried out the drying and dehydrating processing, treatment process is that sample is put on the enamel pallet, evenly shakeouts to place in the baking oven, and 150 ℃ were dried by the fire 4 hours, put in the drying basin standby.
1. respectively get the 30g sample, analyze hetero-ion content with ICP-2000DV, 2. respectively adorn 241mL tetrahydrofuran (THF) 500mL three-necked flask with two, add two each 100g of sample that handle well respectively, stir 60 ℃ of water-bath weighing apparatus temperature, survey number-average molecular weight Mn, molecular weight distribution D, transformation efficiency after 8 hours respectively, colourity relatively.
(1), the icp analysis result is relatively:
Annotate: hetero-ion content unit is ppm
(2), PTMEG catalyzed polymerization activity is tested positive result relatively:
Claims (1)
1. one kind prepares the method that is used for PTMEG polymeric catalyzer, and order comprises the following steps:
A) will dissolve the aqueous solution that is mixed with 10%～30wt% in the technical grade sodium wolframate crystal input water, adding concentration is the agent of 30WT% hydrogen peroxide complex, and the complexing agent add-on is pressed 1.1～1.5 times of sodium wolframate molar weight, stir and be cooled to 3～5 ℃,
B) slowly adding with the sodium wolframate aqueous solution volume ratio is 3～5: 1 18% dilute hydrochloric acid, and whole process maintains the temperature in 3～15 ℃ of scopes,
C) slowly feed SO by gas distributor
2, strict control feeding speed guarantee system temperature is at 5～10 ℃, be reacted to terminal point after, change three sections band filters over to, wash Na in the monitoring washings continuously by 1N, 0.5N, 0.1N dilute hydrochloric acid and deionized water
+% content is less than 5ppm, guarantee sodium ions content in the wolframic acid filter cake less than 100ppm, iron and aluminium composition also all less than the high-purity activity wolframic acid of 10ppm.
D) the high-purity activity wolframic acid with preparation joins in 0.1 ± 0.025mol/L phosphate aqueous solution immediately, the concentration of active tungstic acid is controlled at 1.5 ± 0.25mol/L, fully stirred 2-4 hour, slowly be warming up to 50 ℃～80 ℃ reaction solution clears then, continue the boiling that heats up, continue to be concentrated into terminal point, terminal point is judged by weight.
It is characterized in that also comprising:
E) concentrated solution is put into screw-pushing type refrigeration crystallizer and is carried out crystallisation by cooling, will contain the mother liquor centrifugation of crystal weight 5%～8%,
F) the gained dissolution of crystals is mixed with ether that 50% aqueous solution adds equal-volume C3～C20 extract HPA ether adducts, use isopyknic 0.05%～0.15% Diluted Acid Washing ether adducts again, it is zero high purity 12-tungstophosphoric acid catalyst that ether adducts intensification condensing crystal is obtained sodium ion≤20ppm, iron ion≤5ppm, aluminum ion≤5ppm, arsonium ion≤5ppm, heavy metal content≤2ppm, insoluble in water thing.
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| CNB2003101153970A CN1219599C (en) | 2003-11-21 | 2003-11-21 | PTMEG polymerization catalyst preparation method |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106082343A (en) * | 2016-08-26 | 2016-11-09 | 中南大学 | A kind of purification process of phosphotungstic acid crystal |
| CN106186075A (en) * | 2016-08-26 | 2016-12-07 | 中南大学 | A kind of method preparing phosphotungstic acid crystal from the mixture of sulfuric phosphoric acid solution of tungstenic |
| CN106277060A (en) * | 2016-08-26 | 2017-01-04 | 中南大学 | A kind of preparation method of phosphotungstic acid |
| CN106335928A (en) * | 2016-08-26 | 2017-01-18 | 中南大学 | Method of preparing phosphotungstic acid from sodium tungstate as raw material |
| US11214495B2 (en) | 2016-08-26 | 2022-01-04 | Central South University | Preparation method of phosphotungstic acid |
-
2003
- 2003-11-21 CN CNB2003101153970A patent/CN1219599C/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106082343A (en) * | 2016-08-26 | 2016-11-09 | 中南大学 | A kind of purification process of phosphotungstic acid crystal |
| CN106186075A (en) * | 2016-08-26 | 2016-12-07 | 中南大学 | A kind of method preparing phosphotungstic acid crystal from the mixture of sulfuric phosphoric acid solution of tungstenic |
| CN106277060A (en) * | 2016-08-26 | 2017-01-04 | 中南大学 | A kind of preparation method of phosphotungstic acid |
| CN106335928A (en) * | 2016-08-26 | 2017-01-18 | 中南大学 | Method of preparing phosphotungstic acid from sodium tungstate as raw material |
| CN106335928B (en) * | 2016-08-26 | 2017-11-07 | 中南大学 | A kind of method that phosphotungstic acid is prepared by raw material of sodium tungstate |
| US11214495B2 (en) | 2016-08-26 | 2022-01-04 | Central South University | Preparation method of phosphotungstic acid |
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