CN1915512A - Catalyst for alkylation of toluene methanol - Google Patents
Catalyst for alkylation of toluene methanol Download PDFInfo
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- CN1915512A CN1915512A CNA2005100287695A CN200510028769A CN1915512A CN 1915512 A CN1915512 A CN 1915512A CN A2005100287695 A CNA2005100287695 A CN A2005100287695A CN 200510028769 A CN200510028769 A CN 200510028769A CN 1915512 A CN1915512 A CN 1915512A
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- catalyst
- alkylation
- molecular sieve
- toluene methanol
- toluene
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- 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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Abstract
A catalyst for alkylating the phenyl ring of toluene or methol to prepare xylene with high conversion rate and selectivity features that the RE metal is carried by hydrogen-type ZSM-5 main body.
Description
Technical field
The present invention relates to a kind of catalyst that is used for alkylation of toluene methanol, particularly about being used for the alkylating catalyst of methylbenzene methanol phenyl ring.
Background technology
Methylbenzene methanol phenyl ring methylation reaction can change into toluene the higher dimethylbenzene of using value, and wherein the dimethylbenzene product is the equilibrium composition mixture of its three isomers, and the paraxylene that has the call only accounts for about 24%.Therefore there is the people to propose the methylated new technology of methylbenzene methanol selectivity phenyl ring, makes reaction system optionally generate paraxylene.After the beginning of the seventies, ZSM-5 was synthesized and since it to alkylation, isomerization, phenyl ring methylate, selective cracking process and by reactions such as methanol synthesized gasoline have the uniqueness catalytic performance, extensively paid attention to.The ZSM-5 zeolite constitutes pore canal system by 10 yuan of oxygen rings, has medium sized aperture and aperture.The aperture characteristics permission molecular diameter of ZSM-5 zeolite is that the paraxylene of 0.63 nanometer spreads rapidly, can seriously hinder ortho-xylene and meta-xylene diffusion that molecular diameter is 0.69 nanometer simultaneously.In toluene phenyl ring methylation reaction system, there is following relation in the diffusion coefficient of each species in the ZSM-5 duct: benzene 〉=toluene＞ethylbenzene ≈ paraxylene＞ortho-xylene ≈ meta-xylene, this fact means carries out the possibility that shape is selected to toluene phenyl ring methylation reaction, can obtain to be higher than in the dimethylbenzene product paraxylene content of isomer of thermodynamical equilibrium concentration far away.Because the outer surface acidity position is to the isomerization of the rich contraposition product non-selectivity that diffuses out in the duct, so end product still is equilibrium composition.In order to obtain having the catalyst of higher para-selectivity, the ZSM-5 molecular sieve is carried out modification be necessary.
The early stage method of modifying that adopts mainly is phosphorus, magnesium elements modification, and phosphorus, boron modification can play neutralization and promotor action to the molecular sieve surface acidity, and molecular sieve surface strong acid center is reduced, and the weak acid center increases relatively.Strong acid center forms stable meta-isomer easily, and the weak acid center then helps forming para-isomer.In addition, phosphorus can covering catalyst the strong acid center of outer surface, stop the quick isomerization of paraxylene of coming out in the duct, phosphorus can also make the effective dimensions in duct infall or aperture reduce.Catalyst is after phosphorus, boron modification, and also available halide, carbon dioxide, nitrogen-containing compound, sulfur-containing compound are further handled catalyst to improve para-selectivity.But these processing methods can obviously reduce activity of such catalysts, even reaction is carried out under very high temperature, conversion ratio is still not high, and P elements easy loss under reaction condition also is a defective of this technology.
Proposed modification among document U.S. Pat 3965210 and the US4145315, promptly reduced port size and shielding outer surface acidity active sites, preparation methylbenzene methanol phenyl ring alkylation catalyst the ZSM-5 molecular sieve structure.The method of modifying is to select silanes or (gathering) siloxane compound for use, and commonly used is polysiloxane-based.Thereby the meeting thermal decomposition under high temperature action of these silicon-containing compounds is converted into siliceous deposits and plays modifying function, compares with estersil commonly used at present, and price is far cheap, easy industrialization simple to operate.The method that silicon-containing compound is deposited on molecular sieve outer surface is that silicon-containing compound is dissolved in the n-hexane solvent, the impregnated zeolite outer surface, and roasting obtains selecting the catalyst of shapeization again.
Summary of the invention
Technical problem to be solved by this invention be in the past in the document methylbenzene methanol phenyl ring alkylation catalyst have activity and the lower problem of para-selectivity, a kind of new catalyst that is used for alkylation of toluene methanol is provided.This catalyst is used for the alkylation of toluene methanol reaction, has the catalyst activity height, the characteristics that the product para-selectivity is high.
For solving the problems of the technologies described above, the technical solution used in the present invention is as follows: a kind of catalyst that is used for alkylation of toluene methanol by weight percentage, comprises SiO
2/ Al
2O
3Mol ratio is 20～150 Hydrogen ZSM-5 molecular sieve 20～90%, binding agent silica or aluminium oxide 1～75%, on Hydrogen ZSM-5 molecular sieve load thulium or its oxide 0.005～50%.
In technique scheme, Hydrogen ZSM-5 molecular sieve SiO
2/ Al
2O
3The mol ratio preferable range is 40～80, and the consumption preferable range of Hydrogen ZSM-5 molecular sieve is 40～80% by weight percentage; By weight percentage, the thulium preferred version is selected from lanthanum, cerium or its mixture, and its load capacity preferable range is 1～25%.The catalyst preferred version on Hydrogen ZSM-5 molecular sieve also load be selected from least a in magnesium, calcium constituent or its oxide, by weight percentage, load capacity is 0.01～15%, its preferable range is 2～10%; For improving para-selectivity, the catalyst preferred version is handled for flood polysiloxanes again behind shaping of catalyst, the consumption of polysiloxanes is 0.5～50% of a catalyst weight, and its preferable range is 5～30% of a catalyst weight, and the polysiloxanes preferred version is selected from the phenyl methyl polysiloxanes.The consumption preferable range of binding agent silica or aluminium oxide is 10～50% by weight percentage.
Preparation of catalysts method of the present invention is as follows:
With the ZSM-5 molecular sieve is active main body, adopts the method that adds the binding agent extrusion to prepare moulding.The binding agent that adds can be SiO
2Or Al
2O
3, the addition of binding agent is counted between 1% to 75% with its percentage in preformed catalyst butt weight.In catalyst preparation process, introduce required metallic element and carry out modification.The existence form of metallic element can be oxide, hydroxide or salt, and the method for introducing can adopt ion-exchange, dipping or mechanical mixture.The catalyst of moulding is selected the shape processing with for example polysiloxanes of phenyl methyl polysiloxanes, obtains having in methylbenzene methanol phenyl ring methylation reaction the catalyst of very high para-selectivity.
The present invention at least aly in magnesium, calcium constituent or the oxide carried out modification by introducing rare earth metal and be selected from Hydrogen ZSM-5 molecular sieve, weight space velocity 2.0 hours
-1, reaction temperature is 440 ℃, and reaction pressure is 0..5MPa, and hydrogen hydrocarbon mol ratio is to carry out the examination of methylbenzene methanol phenyl ring methylation reaction under 4.0 conditions.These data declaration Hydrogens ZSM-5 molecular sieve is by rare earth metal with after being selected from the modification of magnesium, calcium constituent, again by after handling with the phenyl methyl polysiloxanes, can significantly improve the para-selectivity of activity of such catalysts and product simultaneously, obtain better technical effect.
The invention will be further elaborated below by embodiment.
The specific embodiment
[embodiment 1]
Na
2O content is less than 0.1% (weight), SiO
2/ Al
2O
3Mol ratio is ammonium type ZSM-5 molecular sieve powder 75.0 grams of 50,550 ℃ of calcination losses 10%, adds 42.2 gram Ludox (SiO
2Weight percent content 40%) analyzes pure lanthanum nitrate [La (NO
3)
3NH
2O] the solution equivalent impregnation, oven dry, roasting.Making weight ratio is: La/ Hydrogen ZSM-5 molecular sieve/SiO
2=15/80/20 catalyst A.
[embodiment 2]
Na
2O content is less than 0.1% (weight), SiO
2/ Al
2O
3Mol ratio is 60, the ammonium type ZSM-5 molecular sieve powder of calcination loss 10% 75.0 grams, with Na
2O content is less than the boehmite (α-Al of 0.15% (weight), 550 ℃ of calcination losses 30%
2O
3H
2O) 24.1 grams fully mix, and mediate extruded moulding, dry back roasting pelletizing, with analyzing pure cerous nitrate [Ce (NO
3)
36H
2O] solution impregnation, oven dry, roasting are with analyzing pure magnesium acetate [Mg (CH
3COO)
24H
2O] solution impregnation, oven dry, roasting.Making weight ratio is: the catalyst B of Ce/Mg/ Hydrogen ZSM-5 molecular sieve/aluminium oxide=2/6/80/20.
[embodiment 3]
Na
2O content is less than 0.1% (weight), SiO
2/ Al
2O
3Mol ratio is 80, the ammonium type ZSM-5 molecular sieve powder of calcination loss 10% 75.0 grams, adds the boehmite (α-Al of 64.3 grams and embodiment 2 same sizes
2O
3H
2O), fully mix, mediate extruded moulding, dry back roasting pelletizing, earlier with analyzing pure lanthanum nitrate [La (NO
3)
3NH
2O] the solution equivalent impregnation, oven dry, roasting, magnesium acetate [Mg (CH again
3COO)
24H
2O] the solution equivalent impregnation, calcium nitrate [Ca (NO is used in oven dry, roasting at last
3)
24H
2O] the solution equivalent impregnation, oven dry, roasting.Making weight ratio is: La/Mg/Ca/ Hydrogen ZSM-5 molecular sieve/Al
2O
3=20/6/2/60/40 catalyst C.
[embodiment 4]
Ammonium type ZSM-5 molecular sieve powder 75.0 grams of embodiment 2 add and boehmite 24.1 grams of embodiment 2 same sizes mix the kneading extruded moulding, dry back roasting pelletizing.Earlier analyze pure lanthanum nitrate [La (NO with 0.5N
3)
3NH
2O] 95 ℃ of water-baths of solution exchange 0.5 hour, oven dry, roasting, use 0.2N magnesium acetate [Mg (CH again
3COO)
24H
2O] 95 ℃ of water-baths of solution exchange 0.5 hour, oven dry, roasting.Making weight ratio is: the catalyst D of La/Mg/ Hydrogen ZSM-5 molecular sieve/aluminium oxide=15/3/80/20.
[embodiment 5]
Ammonium type ZSM-5 molecular sieve powder 75.0 grams of embodiment 1, add the boehmite of 24.1 grams and embodiment 2 same sizes, mix, mediate extruded moulding, dry the back roasting, make weight ratio and be: the catalyst E of Hydrogen ZSM-5 molecular sieve/aluminium oxide=75/25.
[embodiment 6～10]
Get 20 gram catalyst A～E respectively, join in the solution that phenyl methyl polysiloxanes and 30 ml n-hexanes are made into, remove n-hexane.Residue speed with 1 ℃/min in muffle furnace of drying is warming up to 538 ℃, keeps cooling naturally after 3 hours, obtain catalyst F～J respectively, wherein catalyst A, B handle with 2.0 gram phenyl methyl polysiloxanes respectively and get catalyst F, G respectively; Catalyst C with 4.0 gram phenyl methyl polysiloxanes handle catalyst H; Catalyst D, E respectively with 3.0 gram phenyl methyl polysiloxanes handle catalyst I and J.
[embodiment 11～20]
With catalyst A～J, on the fixed bed reaction evaluating apparatus, carry out the active and selectivity investigation of toluene phenyl ring methylation reaction.Loaded catalyst is 5.0 grams, and weight space velocity is 2.0 hours
-1, reaction temperature is 440 ℃, and reaction pressure is 0.5MPa, and hydrogen hydrocarbon mol ratio is 4.Reaction result is listed in table 1.
The reaction result of table 1 catalyst A～J
| Instance number | Catalyst | Toluene conversion, % | Para-selectivity, % |
| 11 12 13 14 15 16 17 18 19 20 | A B C D E F G H I J | 34.1 28.3 23.4 23.1 36.4 27.4 17.0 19.6 16.3 27.3 | 70.2 62.1 87.6 40.7 23.9 78.0 80.3 94.0 61.4 67.8 |
Claims (10)
1, a kind of catalyst that is used for alkylation of toluene methanol by weight percentage, comprises SiO
2/ Al
2O
3Mol ratio is 20～150 Hydrogen ZSM-5 molecular sieve 20～90%, on Hydrogen ZSM-5 molecular sieve load thulium or its oxide 0.005～50%, binding agent silica or aluminium oxide are 1～75%.
2,, it is characterized in that the SiO of Hydrogen ZSM-5 molecular sieve according to the described catalyst that is used for alkylation of toluene methanol of claim 1
2/ Al
2O
3Mol ratio is 40～80, and the consumption of Hydrogen ZSM-5 molecular sieve is 40～80% by weight percentage.
3,, it is characterized in that the load capacity of thulium by weight percentage or its oxide is 1～25% according to the described catalyst that is used for alkylation of toluene methanol of claim 1.
4,, it is characterized in that thulium is selected from lanthanum, cerium or its mixture according to the described catalyst that is used for alkylation of toluene methanol of claim 1.
5,, it is characterized in that on the Hydrogen ZSM-5 molecular sieve also load and be selected from least a in magnesium, calcium constituent or its oxide that by weight percentage, load capacity is 0.01～15% according to the described catalyst that is used for alkylation of toluene methanol of claim 1.
According to the described catalyst that is used for alkylation of toluene methanol of claim 5, it is characterized in that by weight percentage that 6, at least a load capacity that is selected from magnesium, calcium constituent or its oxide is 2～10%.
7, according to the described catalyst that is used for alkylation of toluene methanol of claim 1, it is characterized in that flooding the polysiloxanes processing again behind the shaping of catalyst, the consumption of polysiloxanes is 0.5～50% of a catalyst weight.
8, according to the described catalyst that is used for alkylation of toluene methanol of claim 7, the consumption that it is characterized in that polysiloxanes is 5～30% of a catalyst weight.
9, the described according to Claim 8 catalyst that is used for alkylation of toluene methanol is characterized in that polysiloxanes is the phenyl methyl polysiloxanes.
10,, it is characterized in that the consumption of binding agent silica by weight percentage or aluminium oxide is 10～50% according to the described catalyst that is used for alkylation of toluene methanol of claim 1.
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|---|---|---|---|
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|---|---|---|---|
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| CN100443176C CN100443176C (en) | 2008-12-17 |
Family
ID=37736662
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| CN101961659A (en) * | 2010-10-08 | 2011-02-02 | 同济大学 | Shape selective alkylation catalyst for synthesizing toluene and ethanol into p-methyl ethylbenzene |
| CN101970383A (en) * | 2008-03-13 | 2011-02-09 | 弗纳技术股份有限公司 | Process for liquid phase alkylation |
| CN102101818A (en) * | 2009-12-16 | 2011-06-22 | 中国石油天然气股份有限公司 | Method for synthesizing dimethylbenzene by alkylating benzene and methanol |
| CN101456786B (en) * | 2007-12-12 | 2011-12-07 | 中国科学院大连化学物理研究所 | Method for preparing p-xylene and co-producing light olefins by toluene and methylating reagent |
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