CN1485322A - Method for producing tetrahydrofuran - Google Patents
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- CN1485322A CN1485322A CNA021307806A CN02130780A CN1485322A CN 1485322 A CN1485322 A CN 1485322A CN A021307806 A CNA021307806 A CN A021307806A CN 02130780 A CN02130780 A CN 02130780A CN 1485322 A CN1485322 A CN 1485322A
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Abstract
A method of preparing tetramethylene oxide comprises: at the presence of a hydrogenation catalyst, making one of precursor selecting from maleate,succinate and gamma- butyrolactone, or their combinations contact with hydrogen, separating and collecting tetramethylene oxide. The hydrogenation catalyst is composed of a noble metal selecting from Pd, Pt, Ru and Re and a non-noble metal selecting from Zn, Mn, Al, Fe and Ni, which is supported on an inorganic carrier. due to the hydrogenation catalyst, the content of noble metal is low; at a mild pressure, a hydrogenating precursor of maleate,succinate and gamma- butyrolactone could be directly used to prepare tetramethylene oxide, reducing pressure in the liquid phrase.
Description
Technical field
The present invention relates to the preparation method that the tetrahydrochysene furan is fed.
Technical background
Tetrahydrofuran (THF) is lower boiling (66 a ℃) solvent, is particularly suitable for dissolving polyvinyl chloride, polypropylene and polyvinylidene chloride, is commonly used for accurate tape clean-out system or as the protective material of aluminium electroplating bath; Tetrahydrofuran (THF) also is the valuable intermediate of a series of pharmaceutical chemicalss of preparation and plastics, be mainly used in and produce poly-tetramethylene glycol ether, poly-tetramethylene glycol ether is used to make polyurethane elastomeric fiber, and the increasing sharply of polyurethane elastomeric fiber demand promoted increasing sharply to the demand of tetrahydrofuran (THF) indirectly.
In the prior art, the patent of relevant preparation tetrahydrofuran (THF) is a lot, and wherein most patent is from the cis-butenedioic anhydride or derivatives thereof, uses loaded noble metal catalyst, carries out high-pressure liquid phase hydrogenation preparing tetrahydrofuran (THF).US4,550,185 and US4,609,636, be hydrogenation catalyst with 3%wtPd/3%wtRe/C, in 180 ℃ to 230 ℃ temperature range, toxilic acid aqueous solution hydrogenation under greater than the pressure of 17.0MPa is generated tetrahydrofuran (THF) and 1, the mixture of multiple materials such as 4-butyleneglycol; US5,478,952 to disclose with 1%wtRu/4%wtRe/C be hydrogenation catalyst, under the reaction conditions of 250 ℃ and 13.0～17.0MPa from succsinic acid aqueous solution preparation tetrahydrofuran (THF), gamma-butyrolactone and 1, the mixture of 4-butyleneglycol etc.; US5,473,086, JP08141396, JP06157490 etc. disclose the method for working load type noble metal catalyst high-pressure liquid phase hydrogenation preparing tetrahydrofuran (THF).The described catalyzer of these patents all is two or more a precious metal element of load on absorbent charcoal carrier, and the precious metal total content is higher, and is general greater than 5% of catalyzer total mass, makes that the catalyzer manufacturing cost is higher; And use these many noble metal catalysts under very high pressure condition, generally to be higher than 15.0MPa, and tetrahydrofuran (THF) just can be obtained yield preferably, and high top pressure operation has not only increased facility investment but also has increased operation easier.And when pressure was lower than 10.0MPa, product was based on gamma-butyrolactone, and the tetrahydrofuran (THF) yield is low, generally was lower than 40%.US4 in addition, 965,387 have introduced and have used CuO/Cr
2O
3/ ZnO/Al
2O
3Being catalyzer, under the pressure of 4.2MPa, be that the raw material gas phase hydrogenation prepares the tetrahydrochysene furan food in one's mouth and gamma-butyrolactone with the fused cis-butenedioic anhydride, but catalyzer contains great toxicity Cr
2O
3Composition, and need at first raw material to be vaporized, complicated cis-butenedioic anhydride gasification process increased.
Summary of the invention
The purpose of this invention is to provide a kind ofly under lower pressure, adopt non-toxic catalyst to prepare the method for tetrahydrofuran (THF), solve the prior art hypertonia or use the problem of toxic component catalyst by liquid phase catalytic hydrogenation.
Tetrahydrofuran (THF) preparation method provided by the invention comprises: in the presence of hydrogenation catalyst, one or more mixture in the hydrogenatable precursors such as being selected from toxilic acid, succsinic acid and gamma-butyrolactone is contacted with hydrogen, separate and the collection tetrahydrofuran (THF), hydrogenation catalyst wherein is made up of one or more base metals that are selected from a kind of precious metal among palladium Pd, platinum Pt, ruthenium Ru, the rhenium Re and are selected from copper Cu, zinc Zn, manganese Mn, aluminium Al, iron Fe, the nickel that are carried on the inorganic carrier.
The invention is characterized in that catalyzer is to load on the inorganic carrier simultaneously with a kind of precious metal and one or more base metal, described precious metal is selected from a kind of in the metals such as Pd, Pt, Ru, Re, described base metal is selected from one or more in the metals such as Cu, Zn, Mn, Al, Fe, Ni, and described carrier is selected from a kind of in gac, aluminum oxide and the titanium oxide etc.Wherein the charge capacity (with catalyzer gross weight is benchmark) of precious metal element on catalyzer is about 0.1～10%, and preferably 1～6%; The charge capacity of base metal element is about 0.1～30%, and preferably 3～10%.This catalyst composition can also the further modification by sneaking into one or more metals that are selected from IA family or IIA group.
The catalyzer that the present invention uses can be used immersion process for preparing, with solution that contains a kind of precious metal chemical complex and the solution that contains one or more non-noble metal compounds, is divided into one or more impregnation steps, the incipient impregnation inorganic carrier that is:.After each step dipping, the gained catalyzer all is dried and desolvates to remove.Drying temperature is between 30～200 ℃, preferably between about 60～150 ℃.Dried catalyzer need be preferably under about 200～400 ℃ temperature condition at about 150～800 ℃, carries out roasting.Roasting process can carry out under the protection of rare gas element (as nitrogen).
Described catalyzer before use can be in 150～500 ℃ temperature range, preferably in 200～300 ℃ temperature range, reduces with the mixed gas of pure hydrogen or hydrogen and rare gas element (as nitrogen).
The reaction raw materials that the present invention uses is taken from one or more the mixture in the hydrogenatable precursors such as toxilic acid, succsinic acid, gamma-butyrolactone.Wiring solution-forming when toxilic acid, succsinic acid use, solvent can be water, low-carbon alcohol or gamma-butyrolactone, and concentration range can be from the dilute solution to the saturated solution, and general weight percent concentration is about 20～40%.Directly charging of gamma-butyrolactone.The stoichiometry of general hydrogen need surpass the metering that participates in reaction, and unreacted hydrogen can be recycled.Hydrogen gas space velocity is 200～20000hr
-1, preferred 800～15000hr
-1, the liquid hourly space velocity of hydrogenatable precursor is 0.1～20hr
-1, preferred 0.2～15hr
-1
Liquid phase hydrogenation reaction of the present invention can be carried out in batch reactor (as stirred autoclave) and flow reactor multiple reactors such as (as fluidized-bed reactor and fixed-bed reactor).About 150～300 ℃ of temperature of reaction, preferred 200～280 ℃, reaction pressure can be 1～15MPa, preferred 2～10MPa.The hydrogen and the toxilic acid aqueous solution or hydrogenatable precursor such as succsinic acid, gamma-butyrolactone pass through hydrogenation catalyst together in the same way.The reaction product tetrahydrofuran (THF) can effectively be separated by fractionation with by products such as gamma-butyrolactone, succsinic acid, butanols, butyric acid.Wherein succsinic acid and gamma-butyrolactone can optionally be returned hydrotreating stage.
The invention has the advantages that hydrogenation catalyst uses a kind of noble metal component and several base metal combination load on inorganic carrier, the precious metal usage quantity is few, and content is low; Under the middle pressure condition, realize the direct liquid-phase hydrogenatins of hydrogenatable precursor such as toxilic acid, succsinic acid, gamma-butyrolactone are prepared tetrahydrofuran (THF), significantly reduced the pressure condition of liquid-phase hydrogenatin.
Embodiment
The following examples are for composition and catalyzer of the present invention to catalyzer of the present invention are applicable to the response characteristic of middle pressure condition, and never are limitations of the present invention.
In these embodiments, its selectivity is with mole C
4What calculate for the basis (is that selectivity is the C that is converted to product
4The molecular fraction of charging).Charging air speed HLSV and gas space velocity GHSV are that the volume (comprising carrier bulk) with catalyzer calculates.Wherein THF is a tetrahydrofuran (THF), and BDO is 1, and 4-butyleneglycol, GBL are gamma-butyrolactones, and BuOH is a butanols, and BuAC is a butyric acid, and " Others " comprises as by products such as butyl butyrate, propionic acid, propyl alcohol, methane, methyl alcohol.
Embodiment 1
Prepare a kind of precious metal and a kind of base metal and load on catalyzer on the absorbent charcoal carrier: 2%Pd/0.3～1.5%M/C simultaneously, wherein M represents a kind of in the base metal elements such as Cu, Zn, Mn and Al.
Absorbent charcoal carrier is the gac GH-15 that is produced by brilliance timber mill, Beijing.Commercially available GH-15 is a Ф 1.5mm granular active carbon, 40 orders is got in its grinding sieved to 26 purposes.
The preparation of Pd solution is with 12.7g palladium nitrate solution 600ml deionized water dissolving.The preparation of base metal M solution is, gets 1.2g cupric nitrate, 1.4g zinc nitrate, 4.9ml concentration and is 50% manganese nitrate solution or 1.8g aluminum nitrate and use the 120ml deionized water dissolving respectively.
225g (about 100ml) 26～40 purpose gacs with 600ml palladium nitrate solution dipping, are fully stirred, left standstill then 4 hours, 80 ℃ in loft drier dry 12 hours, make 2%Pd/C; Get 25g2%Pd/C,, fully stir, left standstill 4 hours with containing the 120ml solution impregnation of Cu, again 80 ℃ in loft drier dry 12 hours, make catalyzer 2%Pd0.6%Cu/C; Use the same method and make catalyzer: 2%Pd0.6%Zn/C and 2%Pd1.5%Mn/C.Under 300～500 ℃ temperature condition, catalyzer is carried out roasting then, the preceding carrier (nitrate) of each element is decomposed, thereby make each element form with oxide compound on absorbent charcoal carrier exist with nitrogen protection.
5ml (about 2.5g) the catalyzer 5ml fixed-bed micro-reactor of packing into is reduced.Reaction raw materials is a gamma-butyrolactone, and concrete reductive condition is that at first the temperature rise rate with 1 ℃/min is raised to 280 ℃, reduces 12 hours in the presence of hydrogen; The flow of reduction hydrogen is 500ml/min, and pressure is normal pressure.Catalyzer after the reduction is that 250 ℃, pressure are that 6.0MPa, LHSV are 0.36h in temperature
-1, GHSV is 6000h
-1Condition under GBL is carried out hydrogenation, in detail reaction result is listed in the table 1.
Table 1 Pd and a kind of base metal combination catalyst reaction result
Selectivity %
Catalyzer is formed transformation efficiency/%
THF BDO BuOH BuAC Others
2％Pd/C 29.3 6.9 0 4.0 87.6 1.6
2％Pd·0.6％Cu/C 16.6 46.8 0 4.6 47.2 1.5
2％Pd·0.6％Zn/C 16.8 85.6 3.3 1.8 7.7 1.65
2％Pd·1.5％Mn/C 24.8 48.7 0 4.1 43.9 3.3
Embodiment 2
Prepare a kind of precious metal and two kinds of base metals and load on catalyzer on the absorbent charcoal carrier: 2%Pd0.3～1.5%M simultaneously
10.3～1.5%M
2/ C, wherein M
1And M
2Represent a kind of in the base metal elements such as Cu, Zn, Mn and Al respectively.
Prepare 2%Pd/C with method with embodiment 1.Get 1.2g cupric nitrate and 1.4g zinc nitrate 120ml deionized water dissolving, get 25g 2%Pd/C and use dipping method to make catalyzer: 2%Pd0.6%Cu0.6%Zn/C with embodiment 1; Get 1.2g cupric nitrate and 4.9ml concentration and be 50% manganese nitrate solution and prepare catalyzer: 2%Pd0.6%Cu1.5%Mn/C with the method for the above-mentioned catalyzer of preparation; With catalyzer being handled with the heat treating method of embodiment 1.With catalyst reduction condition catalyzer is activated with embodiment 1.Under the reaction conditions with embodiment 1 catalyzer is estimated, detailed reaction result is listed in the table 2.
The catalyst reaction result of table 2 Pd and two kinds of base metal combinations
Transformation efficiency selectivity/%
Catalyzer is formed
/％ THF BDO BuOH BuAC Others
2％Pd·0.6％Cu·0.6％Zn/C 26.68 1.9 0 1.9 15.3 1.0
2％Pd·0.6％Cu·1.5％Mn/C 36.9 52.2 0 2.7 41.4 3.6
Embodiment 3
Prepare a kind of precious metal and three kinds of base metals and load on catalyzer on the absorbent charcoal carrier: 2%Pd0.3～1.5%M simultaneously
10.3～1.5%M
20.3～1.5%M
3/ C, wherein M
1, M
2And M
3Represent a kind of in the base metal elements such as Cu, Zn, Mn and Al respectively.
Method with embodiment 1 prepares 2%Pd/C.Get 1.2g cupric nitrate, 1.4g zinc nitrate and 4.9ml concentration and be 50% manganese nitrate solution, be dissolved into the 120ml mixing solutions, use with the method for embodiment 1 25g 2%Pd/C is flooded preparation 2%Pd0.6%Cu0.6%Zn1.5%Mn/C; Get 1.2g cupric nitrate, 1.8g aluminum nitrate and 4.9ml concentration and be 50% manganese nitrate solution, be dissolved into the 120ml mixing solutions, use the method preparation with embodiment 1: 2%Pd0.6%Cu0.3%Al1.5%Mn/C.Method with embodiment 1 is heat-treated catalyzer.With similarly to Example 1 reductive condition catalyzer is activated.React under the condition identical with embodiment 1, detailed reaction result is listed in the table 3.
The catalyst reaction result of table 3 Pd and three kinds of base metal combinations
Transformation efficiency selectivity/%
Catalyzer is formed
/％ THF BDO BuOH BuAC Others
2％Pd·0.6％Cu·0.6％Zn·1.5％Mn/C 89.7 81.1 0.5 14.0 3.2 1.2
2％Pd·0.6％Cu·0.3％Al·1.5％Mn/C 69.7 77.7 0.2 1.6 19.0 1.4
Embodiment 4
Prepare a kind of precious metal and four kinds of base metals and load to catalyzer on the absorbent charcoal carrier: 2%Pd0.6%Cu0.6%Zn1.5%Mn0.3%Al/C simultaneously
Method with embodiment 1 prepares 2%Pd/C.With 1.2g cupric nitrate, 1.4g zinc nitrate, 4.9ml concentration is 50% manganese nitrate solution and 1.75g aluminum nitrate 115ml deionized water dissolving, obtains about 120ml base metal nitrate mixed solution.The above-mentioned 25g 2%Pd/C that makes of method dipping with embodiment 1 makes catalyzer: 2%Pd0.6%Cu0.6%Zn1.5%Mn0.3%Al/C.Method with embodiment 1 is heat-treated catalyzer.With similarly to Example 1 reductive condition catalyzer is activated.At 230～270 ℃ of temperature, pressure 2～8.0MPa, LHSV 0.24～12hr
-1, GHSV 1200～12000h
-r1Condition under to the gamma-butyrolactone shortening, experimental result is listed in the table 4.
The catalyst reaction result of table 4 Pd and four kinds of base metal combinations
Reaction conditions selectivity (%)
Transformation efficiency
Temperature, pressure LHSV GHSV
THF BDO BuOH BuAC Others
/℃ /Mpa /h
-1 /h
-1 /％
230 6.0 0.24 6000 62.0 79.8 2.0 11.5 2.2 4.5
250 6.0 0.24 6000 74.8 81.2 0.5 5.8 8.5 4.0
270 6.0 0.24 6000 94.9 71.4 0.1 24.6 1.1 2.8
250 2.0 0.24 6000 67.2 47.8 0.4 4.8 20.6 26.4
250 6.0 0.24 6000 83.0 73.2 1.9 4.6 5.4 14.9
250 8.0 0.24 6000 88.0 79.8 6.1 3.2 1.2 9.7
250 6.0 0.24 6000 99.3 85.1 0 14.5 0 0.4
250 6.0 2.40 6000 26.8 36.1 55.0 0.4 0 8.5
250 6.0 12.0 6000 9.80 16.3 78.3 0.4 0 5.0
250 6.0 0.24 1200 76.6 68.8 0 1.8 22.1 7.3
250 6.0 0.24 6000 91.5 81.5 0 5.7 3.2 9.6
250 6.0 0.24 12000 78.3 84.7 2.1 9 1.4 2.8
Embodiment 5
The toxilic acid aqueous solution with 25% is that raw material carries out catalytic hydrogenation reaction, reaction conditions and result's row and table 5.
Used catalyzer is identical with embodiment 4.
The toxilic acid hydrogenation in aqueous solution reaction result of table 5 pair 25%
Reaction conditions transforms selectivity (%)
Pressure and temp LHSV GHSV leads
THF BDO GBL BuOH BuAC Others
/MPa /℃ /h
-1 /h
-1 /％
6.0 250 0.24 6000 100 72.8 0 9.7 11.5 5.1 0.9
6.0 230 0.24 6000 100 68.3 0 18.9 5.8 6.8 0.2
From the data of table 1～5 as can be seen, the inventive method is the feedstock production tetrahydrofuran (THF) with toxilic acid, succsinic acid or gamma-butyrolactone, can obtain effect preferably under lower pressure.
Claims (9)
1. the preparation method of a tetrahydrofuran (THF), comprise: in the presence of hydrogenation catalyst, make a kind of hydrogenatable precursor that is selected from toxilic acid, succsinic acid and the gamma-butyrolactone or wherein more than one mixture contact with hydrogen, separate and also to collect tetrahydrofuran (THF), hydrogenation catalyst wherein is made up of one or more the base metal that is selected from a kind of precious metal in palladium, platinum, ruthenium, the rhenium and is selected from copper, zinc, manganese, aluminium, iron and the nickel that is carried on the inorganic carrier.
2. according to the described preparation method of claim 1, it is characterized in that described carrier is selected from gac, aluminum oxide and titanium oxide.
3. according to the described preparation method of claim 1, it is characterized in that the charge capacity of precious metal on catalyzer is 0.1～10%, non-noble metal charge capacity is 0.1～30%.
4. according to the described preparation method of claim 1, it is characterized in that the charge capacity of precious metal is 1～6%, non-noble metal charge capacity is 3～10%.
5. according to the described preparation method of claim 1, it is characterized in that, described catalyzer immersion process for preparing, that is: with solution that contains a kind of precious metal chemical complex and the solution that contains one or more non-noble metal compounds, be divided into one or more impregnation steps, the incipient impregnation inorganic carrier, after each step dipping, the gained catalyzer all is dried, drying temperature between 30～200 ℃, the roasting under 150～800 ℃ of conditions of dried catalyzer.
6. according to the described preparation method of claim 1, it is characterized in that, in 150～500 ℃ temperature range, reduce before described catalyzer uses with the mixed gas of pure hydrogen or hydrogen and rare gas element.
7. according to the described preparation method of claim 1, it is characterized in that, wiring solution-forming when toxilic acid, succsinic acid use, strength of solution is 20～40%.
8. according to the described preparation method of claim 1, it is characterized in that hydrogen gas space velocity is 200～20000hr
-1, the liquid hourly space velocity of hydrogenatable precursor is 0.1～20hr
-1, 150～300 ℃ of temperature of reaction, reaction pressure are 1～15MPa.
9. according to claim 1 or 8 described preparation methods, it is characterized in that hydrogen gas space velocity is 800～15000hr
-1, the liquid hourly space velocity of hydrogenatable precursor is 0.2～15hr
-1, 200～280 ℃ of temperature of reaction, reaction pressure are 2～10MPa.
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|---|---|---|---|
| CN 02130780 CN1234701C (en) | 2002-09-28 | 2002-09-28 | Method for producing tetrahydrofuran |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102451681A (en) * | 2010-10-26 | 2012-05-16 | 中化蓝天集团有限公司 | Preparation method for dodecaflurohexane |
| CN102838446A (en) * | 2011-06-21 | 2012-12-26 | 中化蓝天集团有限公司 | Preparation method of 1,1-difluoroethane |
| CN104888802A (en) * | 2015-05-21 | 2015-09-09 | 中国科学院青岛生物能源与过程研究所 | Catalyst for preparing butyric acid and preparation method and application of catalyst |
| CN109836402A (en) * | 2017-11-28 | 2019-06-04 | 中国科学院大连化学物理研究所 | A kind of complex of iridium catalysis cyclic lactone adds the method for hydrogen cyclic ethers |
| CN111905755A (en) * | 2020-07-16 | 2020-11-10 | 浙江恒澜科技有限公司 | Catalyst for hydrogenation of 2,2,4, 4-tetramethyl-1, 3-cyclobutanedione and preparation method and application thereof |
-
2002
- 2002-09-28 CN CN 02130780 patent/CN1234701C/en not_active Expired - Lifetime
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102451681A (en) * | 2010-10-26 | 2012-05-16 | 中化蓝天集团有限公司 | Preparation method for dodecaflurohexane |
| CN102451681B (en) * | 2010-10-26 | 2013-09-04 | 中化蓝天集团有限公司 | Preparation method for dodecaflurohexane |
| CN102838446A (en) * | 2011-06-21 | 2012-12-26 | 中化蓝天集团有限公司 | Preparation method of 1,1-difluoroethane |
| CN102838446B (en) * | 2011-06-21 | 2014-10-08 | 中化蓝天集团有限公司 | Preparation method of 1,1-difluoroethane |
| CN104888802A (en) * | 2015-05-21 | 2015-09-09 | 中国科学院青岛生物能源与过程研究所 | Catalyst for preparing butyric acid and preparation method and application of catalyst |
| CN104888802B (en) * | 2015-05-21 | 2017-03-01 | 中国科学院青岛生物能源与过程研究所 | A kind of for preparing catalyst of butanoic acid as well as preparation method and application thereof |
| CN109836402A (en) * | 2017-11-28 | 2019-06-04 | 中国科学院大连化学物理研究所 | A kind of complex of iridium catalysis cyclic lactone adds the method for hydrogen cyclic ethers |
| CN111905755A (en) * | 2020-07-16 | 2020-11-10 | 浙江恒澜科技有限公司 | Catalyst for hydrogenation of 2,2,4, 4-tetramethyl-1, 3-cyclobutanedione and preparation method and application thereof |
| CN111905755B (en) * | 2020-07-16 | 2022-07-05 | 浙江恒逸石化研究院有限公司 | Catalyst for hydrogenation of 2,2,4, 4-tetramethyl-1, 3-cyclobutanedione and preparation method and application thereof |
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|---|---|
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