CN1820846A - Integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst and its preparation and use - Google Patents
Integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst and its preparation and use Download PDFInfo
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- CN1820846A CN1820846A CN 200610049972 CN200610049972A CN1820846A CN 1820846 A CN1820846 A CN 1820846A CN 200610049972 CN200610049972 CN 200610049972 CN 200610049972 A CN200610049972 A CN 200610049972A CN 1820846 A CN1820846 A CN 1820846A
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Abstract
The integrated member type catalyst for selective oxidation of methyl aromatic hydrocarbon includes carrier, adhesive and active component. The active component is attached via the adhesive onto the carrier, and the carrier is porous honeycomb ceramic material, metal screen or corrugated metal sheet. The active component has the general expression of V1PaXbAlcMdCreOn. The catalyst is superior to available one, which has environmental pollution caused by liquid phase oxidation, complete oxidation and catalyst deactivation of 'hot point' in the catalyst bed, and has high selectivity and excellent industrial application foreground.
Description
(1) technical field
The present invention relates to a kind of integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst and preparation and application, especially for the oxidation of toluene, picoline pendant methyl and the catalyst of ammoxidation reaction.
(2) background technology
Methyl aromatic hydrocarbon side chain selective oxidation is a very important step during fine-chemical intermediate synthesizes.Synthetic aromatic aldehyde, acid, nitrile etc. can be applied in fields such as weaving, agricultural chemicals, medicine, rubber, food.Industrial synthetic technology path is mainly liquid phase oxidation [Bo.HemantV, et al.Ind Eng Chem Prod Res Dev, 1984,23 (3): 455～458] and electrochemical oxidation [Zhu Xian etc., Shanghai University's journal (natural science edition), 2001,7 (1): 73-76].Though these synthetic route technology maturations can cause than serious environmental problem, especially on product separation and equipment corrosion, increased production cost, be unworthy promoting.Therefore people need seek a more synthetic route of greenization.
The gas and solid phase catalyzing selective oxidation is the most economic, reasonable and eco-friendly at present synthetic method because its accessory substance has only water.But the problem that also has the following aspects in commercial Application: 1. activity of such catalysts and selectivity have much room for improvement; 2. reaction belongs to strong exothermal reaction, and reaction bed temperature is difficult to control, and complete oxidation is difficult to eliminate; 3. catalyst easily inactivation and sintering under the long term high temperature environment.
Industrial at selective oxidation, the scientific research personnel has studied the various active catalyst of forming, and proves that now the best catalyst of relative activity is mainly catalytic component based on vanadium, catalyst with base of molybdenum and iron antimony catalyst.And catalytic component based on vanadium is considered to the most potential industrialized catalyst.People such as F.Arena [F.Arena, Appl Catal A, 1999,176:189-199] are to HY molecular sieve, SiO
2, ZrO
2, TiO
2, r-Al
2O
3Study Deng the catalytic component based on vanadium oxide carrier, found V on different carriers
2O
5The reducing power difference, thus the difference of catalyst activity can be caused, think that active best catalyst is V
2O
5/ TiO
2Germany should have the chemistry A.Martin[A.Martin, J Mol Catal A, 2004,211:219-226] investigated alkali metal M (M=Li, Na, K, Rb, Cs) to V
2O
5Active influence finds that alkali metal such as K, Rb, Cs can improve the selectivity of catalytic reaction to aldehyde.S.T.Andersson[S.T.Andersson, J Catal 1991,131:350-368] etc. the people think that Ag adds V
2O
5In the catalyst, obviously improved activity of such catalysts and to the selectivity of benzaldehyde, prevent that the coupled oxidation product from generating, as Ag, Ce during together as auxiliary agent, selectivity that can bigger raising reaction pair oxide side chain, especially the selectivity to aromatic acid can increase, and other auxiliary agent that is studied also has Al, Mg, Te, Mo, Sb etc.; We are [Lu Hanfeng etc., catalysis journal, 2005,26 (2): 101-105] discovery also under study for action, and the adding of P elements can promote V
2O
5Surperficial electrophilicity oxygen species are eliminated in the formation of Lattice Oxygen in the catalyst, thereby improve the selectivity of toluene oxidation.
Many vanadium base granular pattern catalyst have been obtained good result at laboratory stage, but still have many problems in practical application in industry.As the synthetic benzonitrile of amino toluene oxidation, toluene oxidation synthesizing benzaldehyde is the typical case of this class strong exothermal reaction, and thermal discharge is big, very easily causes temperature runaway, makes reaction uncontrollable, thereby causes material complete oxidation and sintering of catalyst inactivation, even cause blast.Therefore if this type reaction is well used industrial, just must solve catalyst granules and bed moves heat problem, control reaction temperature, minimizing deep oxidation product, raising reaction selectivity and controllability.
The industrial fluidized-bed reactor [Chinese patent CN1214959] that generally adopts moves heat problem though can solve beds preferably, but it is higher to the requirement of mechanical strength of catalyst, the vanadium catalyst of metal oxide carrier load is easily broken in fluid bed, and active material easily runs off.And beaded catalyst is when carrying out strong exothermal reaction in fixed bed reactors, bed is unavoidable local " focus " can to occur, usually " focus " located the technological parameter sensitivity, modal is the local temperature runaway of whole beds, the bed layer shaft radial temperature difference is strengthened, thereby cause very fast inefficacy of catalyst and reaction mass by complete oxidation.Many researchers are for addressing this problem, the fixed bed reactors structure is improved, as adding conducting strip or other member [Chinese patent CN2415831] in beds, but, still can't solve the diameter of axle to the big temperature difference because conducting strip has only been removed its peripheral part heat; Secondly catalyst is carried out the inertia dilution [as patent US3801634, JP53-30688B, JP85485], at beds with inert particle segmentation dilute catalyst (adopting different thinner ratios), though this method has been improved the axial uniform temperature of beds preferably, but can not eliminate the high temperature of catalyst particles intragranular, and reduce the production capacity of device; Managing the circulation of outer fused salt, to move heat [patent US4256783, US3147084] be at present industrially to use more technology at strong exothermal reaction, though it can remove the heat of catalyst near the tube wall part basically, if but the thermal conductivity of catalyst granules itself is bad, particle is piled up mutually, still can not eliminate granule interior high temperature and reactor radial symmetry gradient.Under this prerequisite,, study a kind of structure and form that rational catalyst is controlled complete oxidation and bed " focus " has great importance, and good activity and selectivity will be arranged from catalyst itself.
(3) summary of the invention
Problem to be solved by this invention just provides a kind of integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst of high selectivity, and its production and application, especially in the synthetic benzonitrile reaction of amino toluene oxidation.
The technical solution used in the present invention is as follows:
A kind of integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst, the aromatic rings of described methyl aromatic hydrocarbon is phenyl ring or pyridine ring, methyl is arranged on the aromatic rings, at the ortho position, contraposition, between the position on chloro can also be arranged, bromo, methoxyl group, methyl on the described aromatic rings is 1 or 2, described catalyst comprises carrier, jointing material as adhesive layer, active component, described active component by adhesive layer attached on the described carrier, described carrier is the porous honeycomb ceramic carrier, wire mesh structure or wavy metal thin-slab structure carrier, described active component is formed shown in general formula:
V
1P
aX
bAl
cM
dCr
eO
n
V wherein, P, Al, Cr represents vanadium respectively, phosphorus, aluminium, chromium, X represents lithium, sodium, potassium, rubidium, one or more compositions in the caesium, M represents antimony, molybdenum, cerium, tellurium, silver, zinc, manganese, one or more compositions in the cobalt, O represents oxygen, a, b, c, d, e represents the ratio of each element and v element amount of substance respectively,, a=0.5～1.5 wherein, b=0.01～0.2, c=0～0.2, d=0～0.3, e=0～0.2, preferred c=0.01～0.2, e=0.01～0.2, n represents that by in conjunction with oxygen atomicity in the metal oxide that above-mentioned atom generated, n can calculate according to the element valence number, and its value meets stoichiometric relationship.
Further, be that described jointing material is one of following: Al
2O
3, Al
2O
3-TiO
2, Al
2O
3-zeolite, Al
2O
3-SiO
2, Al
2O
3-TiO
2-SiO
2, TiO
2-SiO
2, SiO
2-zeolite, SiO
2-TiO
2-zeolite.
Further, described porous honeycomb ceramic carrier is the carrier of ceramic materials such as cordierite, aluminium oxide, zirconia, silica, the carrier of described wire mesh structure is the silk screen of stainless steel, alloy, and described wavy metal thin-slab structure carrier is that thickness is the Fe-Cr-Al alloy corrugated sheet metal of 0.1mm.
Further, described methyl aromatic hydrocarbon is one of following: toluene, dimethylbenzene, 2-picoline, 3-picoline, methoxy methyl yl pyridines, chlorotoluene, dichlorotoleune, described chlorine can be on ortho position, contraposition or a position, preferred toluene.
The present invention also provides a kind of preparation method of aforesaid integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst, carry out according to following steps: take by weighing the raw material that contains the active component element respectively by active component composition amount, be dissolved in the water, preferred deionized water, add thermal agitation, the control temperature also refluxes, and drips reducing agent, after the solution clarification, stop stirring and obtain catalyst precursor solution; Catalyst precursor solution is concentrated, immersion coating has the carrier of adhesive layer in concentrated solution, be immersed in the precursor solution once more after taking out drying, process to the surface catalyst layer that repeats dip-coating, drying reaches certain thickness, and 300～600 ℃ of roastings promptly obtain described aromatic hydrocarbon side chain catalyst for selective oxidation in air.
In said method, described reducing agent is tartaric acid, oxalic acid, malic acid, hydrochloric acid, hydroxylamine hydrochloride, will control rate of addition in the time of dropping.
The present invention does not directly provide catalyst layer on carrier, and provide catalyst layer by inserting one or more adhesive phases that are mixed and made into such as crystalline aluminum oxide, silicate, silica, titanium oxide therebetween, thereby strengthen the degree of adhesion between carrier and the catalyst layer, prevent that catalyst layer from coming off.Prepare as follows at the carrier that is coated with adhesive layer described in the above-mentioned preparation method: get jointing material and water and be made into finite concentration 10～60%wt with bigger serface, regulator solution pH value to 3～4 again, stir into jointing material slurries with bond properties, with carrier dip-coating in the jointing material slurries, dip-coating again after the drying, the dip-coating drying process is until reaching desired thickness, then 350～600 ℃ of following roastings repeatedly.
According to different jointing materials, corresponding adhesive layer can make respectively in accordance with the following methods:
(1) the single Al on the ceramic integral material
2O
3Its step of the preparation of adhesive layer is as follows: get the γ-Al with bigger serface
2O
3Powder and water are made into finite concentration, regulate the pH of suspension value with nitric acid again, stir into the Al with bond properties
2O
3Slurries.The ceramic honey comb material is at Al
2O
3Dip-coating in the solution, the dip-coating again of back drying is until reaching desired thickness, then 350～600 ℃ of following roastings.
(2) single Al on the metallic carrier
2O
3Its step of the preparation of adhesive layer is as follows: prepare certain density AlCl
3The aqueous solution slowly drips the ammoniacal liquor of a certain amount of concentration, and follows vigorous stirring, after being added dropwise to complete, filters, and with quantitative deionized water washing 3 times, is made into certain density Al (OH) then
3Colloidal solution.Metallic carrier directly immerses Al (OH)
3Colloidal solution, dip-coating at least 3 times is then 350～600 ℃ of following roastings.
(3) preparation process of aluminium oxide-titanium oxide adhesive layer is as follows: get the γ-Al with bigger serface
2O
3Powder and TiO
2Powder and water are made into finite concentration, regulate the pH of suspension value with nitric acid again, stir into the Al with bond properties
2O
3-TiO
2Slurries.The ceramic honey comb material is at Al
2O
3Dip-coating in the solution, the dip-coating again of back drying is until reaching desired thickness, then 350～600 ℃ of following roastings.
(4) preparation process of aluminium oxide-Zeolite bound layer is as follows: get the γ-Al with bigger serface
2O
3Powder and zeolite (can be MFI type zeolite, modenite, ZSM-5, beta-zeolite, faujasite, erionite, their Si/Al be greater than 100) are made into finite concentration with water, regulate the pH of suspension value with nitric acid again, stir into the Al with bond properties
2O
3-TiO
2Slurries.The ceramic honey comb material is at Al
2O
3Dip-coating in the solution, the dip-coating again of back drying is until reaching desired thickness, then 350～600 ℃ of following roastings.
(5) preparation process of silica-aluminium oxide adhesive layer is as follows: concentration adds the γ-Al of high-specific surface area in 20～25% Ludox
2O
3, two kinds of materials mix stirring, are mixed with certain density slurries, and the monolithic devices carrier 350～600 ℃ of following roastings, obtains SiO then by continuous dip-coating drying
2-Al
2O
3Adhesive layer.
(6) preparation process of silica-titanium oxide adhesive layer is as follows: concentration adds the TiO of high-specific surface area in 20～25% Ludox
2, two kinds of materials mix stirring, are mixed with certain density slurries, and the monolithic devices carrier 350～600 ℃ of following roastings, obtains SiO then by continuous dip-coating drying
2-TiO
2Adhesive layer.
(7) preparation process of silica-Zeolite bound layer is as follows: concentration is in 20～25% Ludox, the zeolite that adds high-specific surface area (can be MFI type zeolite, modenite, ZSM-5, beta-zeolite, faujasite, erionite, their Si/Al is greater than 100), two kinds of materials mix stirring, be mixed with certain density slurries, the monolithic devices carrier 350～600 ℃ of following roastings, obtains SiO then by continuous dip-coating drying
2-Zeolite bound layer.
(8) preparation process of silica-aluminium oxide-titanium oxide adhesive layer is as follows: concentration adds the γ-Al of high-specific surface area in 20～30% Ludox
2O
3And TiO
2, three kinds of materials mix stirring, are mixed with certain density slurries, and the monolithic devices carrier 350～600 ℃ of following roastings, obtains SiO then by continuous dip-coating drying
2-Al
2O
3-TiO
2Adhesive layer.
(9) preparation process of silica-zeolite-titanium oxide adhesive layer is as follows: concentration adds the zeolite and the TiO of high-specific surface area in 20～30% Ludox
2(can be MFI type zeolite, modenite, ZSM-5, beta-zeolite, faujasite, erionite, their Si/Al be greater than 100), three kinds of materials mix stirring, be mixed with certain density slurries, the monolithic devices carrier 350～600 ℃ of following roastings, obtains SiO then by continuous dip-coating drying
2-TiO
2-Zeolite bound layer.
Further, the raw material that contains the active component element described in the method is meant respectively: phosphorus is phosphorous acid solid or phosphoric acid solution, aluminium is aluminum nitrate, chromium is chromic nitrate or chromium sulfate or dichromic acid amine, lithium, sodium, potassium, rubidium, cesium element be respectively separately nitrate or carbonate separately, the raw material of antimony, molybdenum, cerium, tellurium, silver, zinc, manganese, cobalt is its nitrate, carbonate, acylate separately.
Integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst of the present invention has good application in methyl aromatic hydrocarbon pendant methyl selective oxidation reaction.Described methyl aromatic hydrocarbon is one of following: toluene, dimethylbenzene, 2-picoline, 3-picoline, methoxy methyl yl pyridines, chlorotoluene, dichlorotoleune, described oxidizing reaction temperature is 300～500 ℃, and air speed is 30000～50000ml/h (g cat)
-1
Further, being applied as in the amino toluene oxidation reaction of described aromatic hydrocarbon side chain catalyst for selective oxidation generates application in the benzonitrile reaction, and reaction temperature is 400 ℃, and air speed is 40000ml/h (g cat)
-1
The present invention compared with prior art, its advantage (beneficial effect) is embodied in:
Overcome liquid-phase oxidation the environmental problem that may cause, also overcome reaction bed temperature and be difficult to control, the complete oxidation that bed " focus " causes and the problem of catalysqt deactivation sintering, in methyl aromatic hydrocarbon side chain selective oxidation reaction, have higher selectivity, have favorable industrial application prospect.
(4) specific embodiment:
Below with specific embodiment technical scheme of the present invention is described, but protection scope of the present invention is not limited thereto:
Embodiment 1
10 gram vanadic anhydrides, 5 gram phosphorous acid, 1.2 gram antimony oxides, 0.2 gram aluminum nitrate, 0.2 gram chromic nitrate, 0.3 gram potassium nitrate are dissolved in the 500ml deionized water, are mixed with solution (1); Get 11g oxalic acid and be dissolved in the 100ml deionized water, be mixed with solution (2).
Control 100～110 ℃ of the temperature of solution (1) with oil bath, stir also and reflux.Slowly drip solution (2) and obtain solution (3) to solution (1).After dropwising, continue heating agitating solution (3) and become clarification up to solution, at 60 ℃ of following decompression distillation solution (3), remove part water, make 600ml be concentrated into 300ml, it is stand-by to obtain catalyst precarsor.Getting specific area is 200～300g/m
2γ-Al
2O
3Powder 100 grams join in the 200ml deionized water, stir, and drip nitric acid adjusting pH of suspension=4.0, stir into the Al with bond properties then
2O
3Slurries.
The ceramic honey comb material is a cordierite, 70mm * 70mm * 70mm specification.The slot diameter is 3mm, and percent opening is more than 95%.
Ceramic honeycomb carrier is at Al
2O
3Take out after the dip-coating in the slurries,, make Al with pressure-air winding-up carrier duct
2O
3Even in the integral carriers surface-coated.Descend dry 5h at 110 ℃ then, and then be immersed in Al
2O
3In the slurries, more than 3 times, increased more than 5% of honeycomb ceramic carrier up to weight with the quadrat method dip-coating processing.The integral carriers for preparing obtains the surface and has Al 500 ℃ of following roastings
2O
3The ceramic honeycomb carrier of adhesive layer.
Having Al
2O
3The ceramic honeycomb carrier of adhesive layer is immersed in the catalyst precursor solution, and dipping 1h takes out back drying under 110 ℃, and the dipping again that uses the same method then is more than 5% of carrier total amount up to the dipping total amount, again at 550 ℃ of following muffle furnace roasting 5h.
The ratio that constitutes the catalyst activity composition is:
V
1P
1.1K
0.05Al
0.01Sb
0.1Cr
0.01O
11
Embodiment 2
It is stand-by to prepare catalyst precarsor according to the method for embodiment 1.
Prepare the 200ml AlCl of certain 1M
3The aqueous solution slowly is added drop-wise to the 800ml ammonia spirit of 10wt%, and follows vigorous stirring, after precipitation reaction is finished, continues to stir 3h, and aging 5h obtains Al (OH)
3Precipitation suspension, after the filtration, filter cake washs 3 times with the 500ml deionized water, is made into the Al (OH) of 1.1g/ml concentration then
3Colloidal solution.
Wavy metal shape light sheet material is the FeCrAl alloy, 80mm * 80mm * 0.1mm (long * wide * thick) specification is soaked 30min at 2wt% sulfuric acid earlier, gets final product with 100ml deionized water washed twice, calcine 10h under 850 ℃ of air then in muffle furnace, obtaining the surface has Al
2O
3The material of whisker.
The sheet metal carrier directly immerses Al (OH)
3Colloidal solution floods 4 times at least, then at 550 ℃ of following roasting 4h.
Having Al
2O
3The sheet metal carrier impregnation of adhesive layer is in catalyst precursor solution, and dipping 1h takes out back drying under 110 ℃, and the dipping again that uses the same method then is more than 5% of carrier total amount up to the dipping total amount, again at 550 ℃ of following muffle furnace roasting 5h.
Embodiment 3.
It is stand-by to prepare catalyst precarsor according to the method for embodiment 1.
Be mixed with the Al (OH) of 1.1g/ml concentration according to the method for embodiment 2
3Colloidal solution is stand-by.
The woven wire material is 316L stainless steel 3 * 7cm, and hole size is 30 orders, and silk screen soaks 1h earlier in 2% sulfuric acid, use 100ml deionized water washes clean then.Adopt electrophoretic deposition (EPD) at silk screen surface-coated one deck Al
2O
3The concrete preparation process of EDP method is: get aluminium powder 0.8 gram (average grain diameter is 5um), polyacrylic acid (PAA) 0.0032 gram and triethylamine 0.02 gram (TEA) and add in the 400ml ethylene glycol, stir and form aluminium powder suspension, then at the ultrasonic 30min that handles down, adopt 30 purpose woven wires as electrode, interelectrode distance is 1cm, and operating voltage is 100V, sedimentation time 2min.The surface is deposited the woven wire of aluminium powder and calcines 3h under 850 ℃ of argon shield, and then in air 500 ℃ the calcining 5h, obtain surface-coated Al
2O
3The web material of/Al.
Treated woven wire directly immerses stand-by Al (OH)
3Colloidal solution floods 4 times at least, then at 550 ℃ of following roasting 4h.
Having Al
2O
3The wire mesh carrier of adhesive layer is immersed in the catalyst precursor solution, and dipping 1h takes out back drying under 110 ℃, and the dipping again that uses the same method then is more than 5% of carrier total amount up to the dipping total amount, again at 550 ℃ of following muffle furnace roasting 5h.
Embodiment 4
It is stand-by to prepare catalyst precarsor according to the method for embodiment 1.
Getting specific area is 200～300g/m
2γ-Al
2O
3Powder 70 grams are 100g/m with 30 gram specific surfaces
2About TiO
2(anatase) mixes, and joins in the 200ml deionized water, stirs, and drips nitric acid adjusting pH of suspension=4.0, stirs into the Al with bond properties then
2O
3-TiO
2Slurries.
Apply Al with the method for implementing 1 at the ceramic honeycomb material surface
2O
3-TiO
2Adhesive layer.
Then having Al
2O
3-TiO
2The ceramic honeycomb carrier of adhesive layer is immersed in the catalyst precursor solution, and dipping 1h takes out back drying under 110 ℃, and the continuous impregnating that uses the same method again is more than 5% of carrier total amount up to the dipping total amount, again at 550 ℃ of following muffle furnace roasting 5h.
Embodiment 5
It is stand-by to prepare catalyst precarsor according to the method for embodiment 1.
Getting specific area is 200～300g/m
2γ-Al
2O
3(silicon oxide particle average diameter 13nm pH3.4) mixes powder 70 grams, adds in the 100ml deionized water again, stirs, and makes the Al with bond properties with 100 grams, 25% Ludox
2O
3-SiO
2Slurries.
Apply Al with the method for implementing 1 at the ceramic honeycomb material surface
2O
3-SiO
2Adhesive layer.
Then having Al
2O
3-SiO
2The ceramic honeycomb carrier of adhesive layer is immersed in the catalyst precursor solution, and dipping 1h takes out back drying under 110 ℃, and the continuous impregnating that uses the same method again is more than 5% of carrier total amount up to the dipping total amount, again at 550 ℃ of following muffle furnace roasting 5h.
Embodiment 6
Except following difference, prepare catalyst precarsor by the method for embodiment 1.
Vanadium raw materials changes ammonium metavanadate 6.4 grams into, and the phosphorous acid amount increases to 6.5 grams, adds 1.0 gram cerous nitrates, does not add antimony oxide, and reducing agent uses hydroxylamine hydrochloride.
Other preparation method is identical with embodiment 5.
Catalyst activity consists of:
V
1P
1.4K
0.05Al
0.01Ce
0.05Cr
0.01O
12.5
Embodiment 7
It is stand-by to prepare catalyst precarsor according to the method for embodiment 6.
50 gram zeolite (ZSM-5; SiO
2/ Al
2O
3=500) ball milling becomes 5 μ m particles, and (silicon oxide particle average diameter 13nm pH3.4) mixes stirring, makes slurries with 120 grams, 25% Ludox then.
These slurries are applied to handle wavy metal shape light sheet materials as the described methods of embodiment 2 (surface contains Al
2O
3Whisker), then at 110 ℃ of following dry 4h, roasting 2h under 400 degree again, obtaining surperficial adhesive layer is SiO
2The sheet metal carrier of-ZSM-5.
Having SiO
2The sheet metal carrier impregnation of-ZSM-5 adhesive layer is in catalyst precursor solution, and dipping 1h takes out back drying under 110 ℃, and the dipping again that uses the same method then is more than 5% of carrier total amount up to the dipping total amount, again at 550 ℃ of following muffle furnace roasting 5h.
Embodiment 8
It is stand-by to prepare catalyst precarsor according to the method for embodiment 6.
40 gram zeolite (ZSM-5; SiO
2/ Al
2O
3=500) ball milling becomes 5 μ m particles, then with 120 the gram 25% Ludox (silicon oxide particle average diameter 13nm, pH3.4), 40 the gram TiO
2(anatase) mixes stirring, makes slurries.
These slurries are applied to handle wavy metal shape light sheet materials as the described methods of embodiment 2 (surface contains Al
2O
3Whisker), then at 110 ℃ of following dry 4h, roasting 2h under 400 degree again, obtaining surperficial adhesive layer is SiO
2-ZSM-5-TiO
2The sheet metal carrier.
Having SiO
2-ZSM-5-TiO
2The sheet metal carrier impregnation of adhesive layer is in catalyst precursor solution, and dipping 1h takes out back drying under 110 ℃, and the dipping again that uses the same method then is more than 5% of carrier total amount up to the dipping total amount, again at 550 ℃ of following muffle furnace roasting 5h.
Embodiment 9
Catalyst according to the ceramic honeycomb carrier load of embodiment 5 preparation is used for the synthetic benzonitrile reaction of amino toluene oxidation.
Reactor is 70mm * 70mm * 100mm (length * wide * height) stainless steel reactor, and interface is a flange, the reactor inlet temperatures thermocouple monitoring.In reactor bed, place a honeycomb substrate catalyst (7070mm * 70mm * 70mm specification).Feeding gas is formed volume ratio: toluene/ammonia/air=1/4/25.Air speed is 40000ml/h (g cat)
-1, reaction temperature is 400 ℃, and the benzonitrile selectivity reaches 95% behind the 10h, and productive rate reaches 80%.
Benzonitrile selectivity calculating formula is:
Benzonitrile calculation of yield formula is:
Claims (10)
1. integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst, the aromatic rings of described methyl aromatic hydrocarbon is phenyl ring or pyridine ring, methyl is arranged on the aromatic rings, methyl on the described aromatic rings is 1 or 2, described catalyst comprises carrier, the jointing material as adhesive layer, active component, described active component by adhesive layer attached on the described carrier, described carrier is porous honeycomb ceramic carrier, wire mesh structure or wavy metal thin-slab structure carrier, and described active component is formed shown in general formula:
V
1P
aX
bAl
cM
dCR
eO
n
Wherein V, P, Al, Cr represent vanadium, phosphorus, aluminium, chromium respectively, X represents one or more compositions in lithium, sodium, potassium, rubidium, the caesium, M represents one or more compositions in antimony, molybdenum, cerium, tellurium, silver, zinc, manganese, the cobalt, O represents oxygen, a, b, c, d, e represent the ratio of each element and v element amount of substance respectively, a=0.5～1.5 wherein, b=0.02～0.4, c=0～0.2, d=0.01～0.3, e=0～0.3, n represents by in conjunction with oxygen atomicity in the metal oxide that above-mentioned atom generated.
2. integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst as claimed in claim 1 is characterized in that described methyl aromatic hydrocarbon, also has chloro, bromo or methoxyl group on the ortho position of aromatic rings, contraposition or the position.
3. integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst as claimed in claim 1 is characterized in that described jointing material is one of following: Al
2O
3, Al
2O
3-TiO
2, Al
2O
3-zeolite, Al
2O
3-SiO
2, Al
2O
3-TiO
2-SiO
2, TiO
2-SiO
2, SiO
2-zeolite, SiO
2-TiO
2-zeolite.
4. integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst as claimed in claim 1 is characterized in that described wavy metal thin-slab structure carrier is that thickness is the Fe-Cr-Al alloy corrugated sheet metal of 0.1mm.
5. integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst as claimed in claim 1 is characterized in that described methyl aromatic hydrocarbon is one of following: toluene, dimethylbenzene, 2-picoline, 3-picoline, methoxy methyl yl pyridines, chlorotoluene, dichlorotoleune.
6. the preparation method of an integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst as claimed in claim 1, it is characterized in that described catalyst is prepared in accordance with the following methods: take by weighing the raw material that contains the active component element respectively by active component composition amount, be dissolved in the water, add thermal agitation, the control temperature also refluxes, drip reducing agent, after the solution clarification, stop stirring and obtain catalyst precursor solution; Catalyst precursor solution is concentrated, immersion coating has the carrier of adhesive layer in concentrated solution, be immersed in the precursor solution once more after taking out drying, process to the surface catalyst layer that repeats dip-coating, drying reaches certain thickness, and 300～600 ℃ of roastings promptly obtain described aromatic hydrocarbon side chain catalyst for selective oxidation in air.
7. the preparation method of integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst as claimed in claim 6, it is characterized in that the described carrier that is coated with adhesive layer prepares as follows: get the solution that jointing material with bigger serface and water are made into 10～60wt%, regulate pH of suspension value to 3～4 again, stir into jointing material slurries with bond properties, with carrier dip-coating in the jointing material slurries, dip-coating again after the drying, the dip-coating drying process is until reaching desired thickness, then 350～600 ℃ of following roastings repeatedly.
8. the preparation method of integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst as claimed in claim 6, it is characterized in that the described raw material that contains the active component element is meant respectively: phosphorus is phosphorous acid solid or phosphoric acid solution, aluminium is aluminum nitrate, chromium is chromic nitrate or chromium sulfate or dichromic acid amine, lithium, sodium, potassium, rubidium, cesium element be respectively separately nitrate or carbonate separately, the raw material of antimony, molybdenum, cerium, tellurium, silver, zinc, manganese, cobalt is its nitrate, carbonate, acylate separately.
9. as the application of the described integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst of claim 1～5 in methyl aromatic hydrocarbon side chain selective oxidation reaction.
10. the application of integrated member type methyl aromatic hydrocarbon selective oxidizing catalyst as claimed in claim 9, it is characterized in that described selective oxidation reaction is an ammoxidation reaction, its reaction temperature is 300～500 ℃, and air speed is 30000～50000ml/h (g cat)
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| CN110419126A (en) * | 2017-07-12 | 2019-11-05 | 株式会社Lg化学 | Cathode for lithium secondary battery and the lithium secondary battery including the cathode and the method for preparing the cathode |
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| CN1024633C (en) * | 1989-03-17 | 1994-05-25 | 武汉大学 | Catalyst containing ortho chloro-toluene-ammonia oxidant and ortho chlorobenzoyl cyanide |
| CN1021548C (en) * | 1989-05-10 | 1993-07-14 | 湘潭市染料化工厂 | Ammonia oxidation catalyst for ortho-chlorotoluene |
| CN1055028C (en) * | 1997-01-13 | 2000-08-02 | 武汉大学 | New catalyst for preparing 2,6-dichlorobenzyl nitrile by ammonia oxidation process |
| DE69802189T2 (en) * | 1997-06-04 | 2002-06-06 | Sasol Tech Pty Ltd | METHOD FOR PRODUCING A VANADIUM PHOSPHOROXIDE CATALYST |
| CN1133619C (en) * | 2002-04-23 | 2004-01-07 | 武汉大学 | Process for preparing 2-fluoro-6-chlorophenyl nitrile |
| JP5076271B2 (en) * | 2003-09-29 | 2012-11-21 | 三菱瓦斯化学株式会社 | Process for the production of alkyl and / or cycloalkyl substituted cyclic nitriles |
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| US11710815B2 (en) | 2017-07-12 | 2023-07-25 | Lg Energy Solution, Ltd. | Negative electrode for lithium secondary battery, lithium secondary battery comprising the same, and method of preparing the negative electrode |
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