CN100389172C - Composition with desulfation function - Google Patents

Composition with desulfation function Download PDF

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CN100389172C
CN100389172C CNB2004100802333A CN200410080233A CN100389172C CN 100389172 C CN100389172 C CN 100389172C CN B2004100802333 A CNB2004100802333 A CN B2004100802333A CN 200410080233 A CN200410080233 A CN 200410080233A CN 100389172 C CN100389172 C CN 100389172C
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composition
heavy
molecular sieve
vapo
vanadium
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CN1754941A (en
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郑金玉
宗保宁
慕旭宏
舒兴田
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Sinopec Research Institute of Petroleum Processing
China Petroleum and Chemical Corp
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Sinopec Research Institute of Petroleum Processing
China Petroleum and Chemical Corp
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Abstract

The present invention discloses a composition with a desulfuring function, which is characterized in that the composition contains a molecular sieve whose skeleton structure contains vanadium elements and second metallic element M to serve as a desulfuring component. The second metal M is selected from one kind of periodic tables IIA, IIB, IVB, VIB, VIIB, VIIIB or lanthanide rare earth elements. The composition can be applied to catalytic cracking reaction, and can effectively reduce the gasoline sulfur content in an FCC course and enhance the hydrothermal stability of FCC catalyst under the condition of no influence on the conventional FCC operating conditions.

Description

A kind of composition with desulfidation
Technical field
The invention relates to a kind of composition, the composition of further saying so and containing molecular sieve as the desulfurization constituent element about a kind of with desulfidation.
Background technology
Fluid catalytic cracking (FCC) is a kind of oil refining process, and the residual oil that is about to heavy ends such as vacuum distillate or more heavy constituent is converted into the main process of the less cut of molecule, existing large-scale commercial applications in refining of petroleum.Catalytically cracked material contains the sulphur that exists with the organosulfur compound form usually, for example mercaptan, thioether, thiophene and substituted thiophene etc., in cracking process, pass through to decompose non-thiophene sulfide, the sulphur of half can be converted into hydrogen sulfide, therefore very easily there is sulphur impurity in the crackate, they enter in the gasoline fraction with certain proportion, and enter gasoline pool.The distribution of sulphur in crackate is all relevant with stock oil, catalyzer, additive and other certain operations conditions.Because it is to the pay attention to day by day of environment protection, also more and more stricter in recent years at the restriction index of sulfur in gasoline content.Restriction sulfur in gasoline content is not only favourable to environment protection, and also very important for the sulfur poisoning degree that reduces vehicle catalytic converter.
Common desulfurization method is to carry out hydrotreatment removing partial vulcanization compound wherein, thereby reduces the sulphur content in the gasoline.Usually select the FCC raw material is carried out the hydrogenation pre-treatment, perhaps after the FCC process, crackate is carried out hydrotreatment.The former hydrogen-consuming volume is big, and the investment of equipment and running expense are all higher; The latter understands the part alkene in the saturated products, causes the loss of octane value.From the viewpoint of economy, preferably can be in cracking process desulfurization and additional other treating processes.In order to reach this purpose, part Study work concentrates on and remove desulfuration from the flue gas of revivifier, but in fact this method does not have to show effect (the Krishna et.al. that significantly reduces the product sulphur content, Additives Improve FCC Process, Hydrocarbon Processing, 1991,11,59-66); Another part research work then concentrates on the auxiliary agent that has desulfurizing function in the FCC process by interpolation, realizes the direct desulfurization in the FCC process.
To having studies have shown that of desulfurizing function auxiliary agent, some metallic elements such as V, Ni, Cu, Cd, Sn, B, Al, Zn etc. have the function of this respect.For example, Grace Davison company has developed GFS sulfur-lowing catalyst and the GSR sulfur prodegradant that reduces the FCC content of sulfur in gasoline; In US5376608 and US5525210, a kind of cracking catalyst with desulfidation is disclosed, it comprises a kind of zeolite molecular sieve that is scattered on the inorganic oxide carrier, with the alumina material in a kind of load L acid site, the Ni by 1~50%, Cu, Zn, Ag, Cd, In, Sn, Hg, Tl, Pb, Bi, B, Al, element such as Ga or compound loaded formation.In US6482315, disclose a kind of on the non-molecular sieve carrier as alumina material on the sweetening additive of a large amount of vanadium of load (5~10 heavy % vanadium), it is used with the conventional FCC cracking catalyst that contains y-type zeolite can demonstrate the effect that better removes content of sulfur in gasoline.In US2002/0179498A and US2003/0089639A, a kind of catalytic cracking process liquid crackate that is used for reducing is disclosed, the desulfurization catalyst of the sulphur content of pressure gasoline particularly, this catalyzer comprise that a kind of oxidation state that comprises is greater than zero metal component with improve catalyst stability and desulphurizing activated rare earth cerium in Molecular Sieve Pore.Molecular sieve is generally faujusite such as USY, and main desulfurization component is a kind of metal in the 3rd cycle, preferred vanadium.
In CN1261618A and CN1281887A, a kind of desulfurization catalyst composition that is used for reducing catalytic cracking process liquid crackate sulphur content is disclosed, it comprises a kind of porous molecular sieve, and this molecular sieve comprises above oxidation state of zeroth order and the metal component in Molecular Sieve Pore and improves the rare earth component of cracking activity.Molecular sieve is large aperture zeolite such as USY or zeolite beta or mesopore zeolite such as ZSM-5, a kind of metal in main 4 cycles of desulfurization component Chang Weidi, preferred vanadium, rare earth metal preferred cerium.
Because catalyzer do not exist only under the hot conditions of cracking reaction, also will be through the recirculation process of steam stripped and oxidation regeneration, so the stability of catalyzer, particularly hydrothermal stability are very important.But the cracking catalyst with desulfidation above-mentioned is to load on metallic compound and forms on certain carrier, metal ion is on the ion-exchange sites, on hydrothermal stability, have problems, under action of high temperature, the metal of load can be moved on the molecular sieve from original position, not only lose original desulphurizing activatedly, more seriously vanadium can destroy the rock steady structure as active component molecular sieve in the FCC catalyzer, causes whole catalyzer to lose activity at last.
Summary of the invention
The objective of the invention is deficiency at the desulfurization cracking catalyst of metallic compound load in the prior art, a kind of good hydrothermal stability is provided, does not influence the composition of main active component molecular sieve structure, said composition can be used as cracking catalyst and is applied in the fluid catalytic cracking process.
Composition with desulfidation provided by the invention, it is characterized in that said composition contain contain the v element and the second metallic element M in a kind of skeleton structure simultaneously molecular sieve as the desulfurization constituent element, said second metal M is selected from a kind of in periodic table of elements IIA, IIB, IVB, VIB, VIIB, VIIIB or the lanthanide series rare-earth elements, and the adding of this constituent element can more effective raising desulfurization degree.
More particularly, composition provided by the invention, mainly form by active component, desulfurization constituent element, carrier, binding agent etc., said desulfurization constituent element is the molecular sieve that contains the v element and second metal component in the skeleton structure simultaneously, and molecular sieve content preferably accounts for 1~20 heavy % of catalyzer, more preferably 7~15 weighs %.In addition, the ratio preferred 1~50, more preferably 3~20 that contains the molecular sieve of v element in wherein said active component and the skeleton structure.
In the catalyzer provided by the invention, contain the molecular sieve of the v element and second metal component in the said skeleton structure simultaneously, abbreviate the bimetal molecular sieve as, be meant that the vanadium and second metallic element enter the skeleton of molecular sieve, with V 4+/ V 5+And M N+Form is combined in the framework of molecular sieve, molecular sieve as backbone element, the vanadium and second metal exist form with FT-IR, ESR, the common sign of NMR and XPS determined (but reference Vanadosilicate catalysts prepared from different vanadium sources andtheir characteristics in methanol to conversion (A.Miyamoto, D.Medhanavyn and T.Inui, Applied Catalysis, 28 (1986) 89-103), Synthesisand Characterization of the Vanadium-incorporated Molecular SieveVAPO-5 (S.H.Jhung, Y.S.UH and H.Chon, Applied Catalysis 62 (1990) 61-72) and Synthesis, characterization and catalytic properties of vanadiumsilicates with a ZSM-48 structure (A.Tuel and Y.Ben Taarit, AppliedCatalysis A:General, 102 (1993) 201-204)).Wherein said second metal is preferably from metals such as Be, Mg, Ti, Mn, Zn, Fe, Cr, Co or Ce.
Said bimetal molecular sieve can be the V-Si molecular sieve (as M-VS-1 and M-VS-2) that contains second metal (M), wherein vanadium, second metal and silicon are as backbone element, the mol ratio of silicon and vanadium is preferred 10~100, the mol ratio preferred 10~100 of the silicon and second metal; Can be for containing the phosphoric acid vanadium aluminum molecular screen (M-VAPO-n of second metal, as VAPO-5, VAPO-11, VAPO-31, VAPO-17 etc.), wherein vanadium, aluminium, phosphorus and second metal are as backbone element, equally, the aluminium wherein and the mol ratio of vanadium are preferred 10~100, the mol ratio preferred 10~100 of the aluminium and second metal; Also can be for containing the phosphoric acid vanadium sial of second metal, the ratio of silicon and aluminium is arbitrarily, at this moment sial recently characterizes the content of vanadium in the skeleton simultaneously as backbone element with silicon vanadium mole.No matter contain the phosphoric acid vanadium aluminium or the phosphoric acid silicon vanadium aluminum molecular screen of second metal, phosphorus element content does not have obvious influence to the performance of composition in the skeleton.
In the composition provided by the invention, said active component is that conventional cracking catalyst usually adopts, can be various macropores and/or mesoporous molecular sieve, for example Y zeolite and ZSM-5 zeolite etc., they can obtain through modification, the Y zeolite of the containing metal constituent element that obtains as USY, REUSY, REY, REHY or through various metal oxide treated; Said ZSM-5 zeolite can be for rare earth modified or through the ZSM-5 zeolite of rare earth and phosphorus modification (brief note is ZRP, as putting down in writing among the CN1093101A).
In the composition provided by the invention, said carrier is various clays, as kaolin etc.; Said binding agent can be selected from the mixture of one or both or three in silicon sol, aluminium colloidal sol and the pseudo-boehmite.
Composition provided by the invention, owing to introduce the molecular sieve that contains the v element and second metallic element in the skeleton with desulfidation, can be used as fluid cracking catalyst uses, under the situation that does not influence conventional FCC operational condition, effectively reduce the content of sulfur in gasoline of FCC process, and improve the hydrothermal stability of catalyzer; Compare with the catalyzer of the used load vanadium of prior art, v element can stably be present in the framework of molecular sieve, avoided because the migration of vanadium to cracking catalyst activity constituent element, as the Y zeolite structural damage; The introducing of second metal has not only improved the desulfurization performance of catalyzer, has also strengthened the stability of cracking catalyst, improves product and distributes.
Embodiment
The present invention is further illustrated below in conjunction with embodiment, but not thereby limiting the invention.
Among the embodiment, the elementary composition of said bimetal molecular sieve carries out quantitative analysis with X-ray fluorescence spectra (FL) in the catalyzer; Its crystalline phase and degree of crystallinity XRD determining.
The molecular sieve of desulfidation is the VAPO-5 that skeleton contains second metal in the catalyzer of embodiment 1~6.
Embodiment 1
Synthesizing of Ce-VAPO-5 molecular sieve: 15g dry glue powder (Al 2O 3Content 65.8%, the Chang Ling catalyst plant is produced), add water 60mL making beating after 60 minutes to wherein slowly dripping 14g ortho-phosphoric acid solution (phosphorus acid content 85%, Beijing chemical reagent work produces).Stir and add 2.3g vanadylic sulfate (V content 22% after 10 minutes earlier, be dissolved in the 2g water), stir after 5 minutes and to add 0.75g Cerium II Chloride (being dissolved in the 2g water), continue under the room temperature to stir that the speed with 1mL/min adds 16ml template triethylamine (content 98%, Beijing chemical reagent work produces) after 60 minutes.Continue to stir after 1 hour, placed 175 ℃ of dynamic crystallizations of crystallizing kettle 72 hours.Behind the products therefrom filtration washing in 80 ℃ of oven dry, sample in flowing air temperature-programmed calcination (120 ℃, 1 hour; 3 ℃/minute are warming up to 550 ℃, keep 4 hours postcooling to room temperature).The X-ray diffraction of products therefrom (XRD) spectrogram has VAPO-5 molecular sieve feature, and its aluminium vanadium mol ratio is 25, and aluminium cerium mol ratio is 50.
According to the heavy % of Ce-VAPO-510, REUSY molecular sieve 30 heavy %, aluminium colloidal sol 10 heavy %, the catalyzer of pseudo-boehmite 20 heavy % and kaolin 30 heavy % is formed, above-mentioned synthetic Ce-VAPO-5 and above-mentioned each component are mixed, after adding suitable quantity of water and stirring, the spray-dried catalyst A 1 that is prepared into.
Embodiment 2
Synthesizing of Fe-VAPO-5 molecular sieve: the preparation method wherein replaces Cerium II Chloride with iron nitrate with embodiment 1, is contained the aluminium phosphate molecular sieve of vanadium and iron simultaneously.The X-ray diffraction of products therefrom (XRD) spectrogram has VAPO-5 molecular sieve feature, and its aluminium vanadium mol ratio is 20, and the ferro-aluminum mol ratio is 50.
According to the heavy % of Fe-VAPO-510, REUSY molecular sieve 30 heavy %, aluminium colloidal sol 10 heavy %, the catalyzer of pseudo-boehmite 20 heavy % and kaolin 30 heavy % is formed the spray-dried catalyst A 2 that is prepared into.
Embodiment 3
Synthesizing of Mg-VAPO-5 molecular sieve: the preparation method wherein replaces Cerium II Chloride with magnesium chloride with embodiment 1, is contained the aluminium phosphate molecular sieve of vanadium and magnesium simultaneously.The X-ray diffraction of products therefrom (XRD) spectrogram has VAPO-5 molecular sieve feature, and its aluminium vanadium mol ratio is 25, and the magnalium mol ratio is 25.
According to the heavy % of Mg-VAPO-510, REUSY molecular sieve 30 heavy %, aluminium colloidal sol 10 heavy %, the catalyzer of pseudo-boehmite 20 heavy % and kaolin 30 heavy % is formed the spray-dried catalyst A 3 that is prepared into.
Embodiment 4
Synthesizing of Ti-VAPO-5 molecular sieve: the preparation method wherein replaces Cerium II Chloride with titanium sulfate with embodiment 1, is contained the aluminium phosphate molecular sieve of vanadium and titanium simultaneously.The X-ray diffraction of products therefrom (XRD) spectrogram has VAPO-5 molecular sieve feature, and its aluminium vanadium mol ratio is 30, and aluminium titanium mol ratio is 30.
According to the heavy % of Ti-VAPO-510, REUSY molecular sieve 30 heavy %, aluminium colloidal sol 10 heavy %, the catalyzer of pseudo-boehmite 20 heavy % and kaolin 30 heavy % is formed the spray-dried catalyst A 4 that is prepared into.
Embodiment 5
Synthesizing of Mn-VAPO-5 molecular sieve: the preparation method wherein replaces Cerium II Chloride with Manganous chloride tetrahydrate with embodiment 1, is contained the aluminium phosphate molecular sieve of vanadium and manganese simultaneously.The X-ray diffraction of products therefrom (XRD) spectrogram has VAPO-5 molecular sieve feature, and its aluminium vanadium mol ratio is 25, and aluminium manganese mol ratio is 40.
According to the heavy % of Mn-VAPO-510, REUSY molecular sieve 30 heavy %, aluminium colloidal sol 10 heavy %, the catalyzer of pseudo-boehmite 20 heavy % and kaolin 30 heavy % is formed the spray-dried catalyst A 5 that is prepared into.
Embodiment 6
Synthesizing of Zn-VAPO-5 molecular sieve: the preparation method wherein replaces Cerium II Chloride with zinc nitrate with embodiment 1, is contained the aluminium phosphate molecular sieve of vanadium and zinc simultaneously.The X-ray diffraction of products therefrom (XRD) spectrogram has VAPO-5 molecular sieve feature, and its aluminium vanadium mol ratio is 25, and aluminium zinc mol ratio is 50.
According to the heavy % of Zn-VAPO-510, REUSY molecular sieve 30 heavy %, aluminium colloidal sol 10 heavy %, the catalyzer of pseudo-boehmite 20 heavy % and kaolin 30 heavy % is formed the spray-dried catalyst A 6 that is prepared into.
Comparative Examples 1
Comparative catalyst DB-1 consists of: (lattice constant is the REUSY molecular sieve Content of rare earth 68 heavy %) 40 heavy %, aluminium colloidal sol 10 heavy %, pseudo-boehmite 20 heavy %, kaolin 30 heavy %.
Comparative Examples 2
Comparative catalyst DB-2 consists of: the heavy % of VAPO-510, (lattice constant is the REUSY molecular sieve
Figure C20041008023300082
Content of rare earth 68 heavy %) 30 heavy %, aluminium colloidal sol 10 heavy %, pseudo-boehmite 20 heavy %, kaolin 30 heavy %.Wherein the preparation method of VAPO-5 does not just wherein add second metallic element with embodiment 1.
Catalyst A 1~A6 and contrast medium DB-1, the DB-2 of preparation were worn out 8 hours under 800 ℃ of 100% water vapour respectively, carry out the evaluation of cracking reaction.The characteristic parameter that is used for the stock oil of cracking reaction sees Table 1.The cracking performance evaluation result sees Table 2.
Table 1
Density (20 ℃), g/cm 3Refractive power (70 ℃) viscosity (50 ℃), mm 2/ s viscosity (100 ℃), mm 2/ s acid number, mgKOH/g zero pour, ℃ aniline point, ℃ carbon residue, m% 0.9154 1.4926 34.14 6.962 0.27 35 82.0 0.18
Elementary composition C, m% H, m% S, m% N, m% 85.38 12.03 2.0 0.16
Metal content, ppm Ni V Cu Fe Na <0.1 <0.1 0.1 0.5 0.8
Four components, m% stable hydrocarbon aromatic hydrocarbons gum asphalt 64.0 32.0 4.0 0.0
Boiling range, ℃ IBP/5% 10%/30% 50%/70% 90%/95% 329/363 378/410 436/462 501/518
Table 2
Catalyzer DB-1 DB-2 A1 A2 A3 A4 A5 A6
MA(800℃/8h) 70 70 70 70 70 70 70 70
C/O 1.47 1.47 1.47 1.47 1.47 1.47 1.47 1.47
Temperature of reaction/℃ 500 500 500 500 500 500 500 500
Dry gas 2.14 1.79 1.63 1.78 1.51 1.58 1.85 2.11
Liquefied gas 10.18 10.94 10.21 9.05 9.71 8.31 9.70 10.99
Gasoline 54.05 50.14 53.32 53.53 52.61 55.46 52.68 52.00
Diesel oil 20.34 22.33 21.39 20.56 21.72 20.71 21.67 21.53
Heavy oil 10.38 12.00 10.45 12.92 10.93 10.92 11.29 10.63
Coke 2.91 2.80 2.99 2.16 3.52 3.02 2.80 2.74
Amount to 100.0 100.0 100.0 100.0 100.0 100.0 100.0 100.0
Transformation efficiency/m% 69.28 65.67 68.16 66.52 67.34 68.37 67.04 67.84
Yield of light oil/m% 74.39 72.47 74.71 74.10 74.34 76.17 74.36 73.53
Light receipts+liquefied gas/m% 84.57 83.40 84.92 83.14 84.04 84.48 84.06 84.52
Heavy oil/coke 3.56 4.28 3.50 5.99 3.11 3.61 4.03 3.88
Coke/transformation efficiency 0.04 0.04 0.04 0.03 0.05 0.04 0.04 0.04
Content of sulfur in gasoline, mg/L 420.93 290.18 241.54 247.89 262.37 268.70 267.77 253.41
Desulfurization degree % base 31.1 42.6 41.1 37.7 36.2 36.4 39.8
As can be seen from Table 2, catalyst A 1~A6 compares with the comparative catalyst DB-1 that does not add the bimetal molecular sieve, and the sulphur content of gasoline reduces greatly, and desulfurization degree is all above more than 35%; Compare with only having added the comparative catalyst DB-2 that contains vanadium molecular sieve VAPO-5, transformation efficiency increases, and the sulphur content of gasoline be than can further reducing, and sweetening effectiveness is more remarkable.
Embodiment 7
Be that with catalyst A 1 difference of embodiment the REUSY molecular sieve among the A1 substitutes with the rare earth USY molecular sieve of ZnO modification, this molecular sieve is labeled as ZARY, and wherein ZnO content 6 weighs %, and content of rare earth is 10 heavy %, and USY content is 84 heavy %, catalyzer numbering A1 '.
Comparative Examples 3
Comparative catalyst DB-3 consists of: ZARY molecular sieve 40 heavy %, aluminium colloidal sol 10 heavy %, pseudo-boehmite 20 heavy %, kaolin 30 heavy %.Evaluation result sees Table 3.
Comparative Examples 4
Comparative catalyst DB-4 consists of: the heavy % of VAPO-510, ZARY molecular sieve 30 heavy %, aluminium colloidal sol 10 heavy %, pseudo-boehmite 20 heavy %, kaolin 30 heavy %.Evaluation result sees Table 3.
Table 3
Catalyzer DB-3 DB-4 Catalyst A 1 '
MA(800℃/8h) 70 70 70
C/O 1.47 1.47 1.47
Temperature of reaction/℃ 500 500 500
Dry gas 2.01 1.87 1.66
Liquefied gas 10.62 11.23 10.30
Gasoline 53.18 50.36 52.57
Diesel oil 20.65 22.05 21.49
Heavy oil 11.02 12.11 11.13
Coke 2.52 2.38 2.85
Amount to 100.0 100.0 100.0
Transformation efficiency/m% 68.33 65.84 67.38
Yield of light oil/m% 73.83 72.41 74.06
Light receipts+liquefied gas/m% 84.45 83.64 84.36
Heavy oil/coke 4.37 5.09 3.91
Coke/transformation efficiency 0.04 0.04 0.04
Content of sulfur in gasoline, mg/L 431.45 297.21 250.68
Desulfurization degree % base 31.1 41.9
Embodiment 8
The desulfurization component is synthetic Fe-VAPO-5 among the embodiment 2, accounts for 13 heavy %, and USY accounts for 35 heavy %, and (ZRP is phosphorus and rare earth modified ZSM-5 molecular sieve to the heavy % of ZRP10, and the industrial trade mark is ZRP-7, and the Qilu Petrochemical catalyst plant is produced, SiO 2/ Al 2O 3Be 80), aluminium colloidal sol 10 heavy %, pseudo-boehmite 16 heavy %, kaolin 16 heavy %.Catalyzer numbering A2 '.Evaluation result sees Table 4.
Comparative Examples 5
Comparative catalyst DB-5 consists of, USY molecular sieve 48 heavy %, the heavy % of ZRP10, aluminium colloidal sol 10 heavy %, pseudo-boehmite 16 heavy %, kaolin 16 heavy %.Evaluation result sees Table 4.
Comparative Examples 6
Comparative catalyst DB-6 consists of, the heavy % of VAPO-513, USY molecular sieve 35 heavy %, the heavy % of ZRP10, aluminium colloidal sol 10 heavy %, pseudo-boehmite 16 heavy %, kaolin 16 heavy %.Evaluation result sees Table 4.
Table 4
Catalyzer DB-5 DB-6 Catalyst A 2 '
MA(800℃/8h) 70 70 70
C/O 1.47 1.47 1.47
Temperature of reaction/℃ 500 500 500
Dry gas 1.95 1.90 1.91
Liquefied gas 11.68 10.12 10.60
Gasoline 52.26 52.14 52.09
Diesel oil 20.07 20.76 20.77
Heavy oil 11.33 12.87 12.68
Coke 2.71 2.21 1.95
Amount to 100.0 100.0 100.0
Transformation efficiency/m% 68.60 66.37 66.55
Yield of light oil/m% 72.33 72.90 72.86
Light receipts+liquefied gas/m% 84.01 83.02 83.46
Heavy oil/coke 4.18 5.82 6.50
Coke/transformation efficiency 0.04 0.03 0.03
Content of sulfur in gasoline, mg/L 418.34 293.12 256.31
Desulfurization degree % base 29.9 38.7
Embodiment 9~11
The catalyzer of embodiment 9~11 is designated as A7, A8 and A9 respectively, the REUSY molecular sieve content is 35 weight %, pseudo-boehmite 20 heavy %, kaolin content is 30 weight %, difference is that Al/V among the used Ce-VAPO-5 (mol) is 25, Al/Ce (mol) is respectively 120,70 and 20, and content is respectively 8 heavy %, 5 heavy % and 2 heavy %, and the aluminium sol content is respectively 7 heavy %, 10 heavy % and 13 heavy %.Evaluation result sees Table 5, lists file names with the evaluation result of comparative catalyst DB-1 and DB-2 in the table 5.
Table 5
Catalyzer DB-1 DB-2 A7 A8 A9
Al/Ce(mol) 120 70 20
MA(800℃/8h) 70 70 70 70 70
C/O 1.47 1.47 1.47 1.47 1.47
Temperature of reaction/℃ 500 500 500 500 500
Dry gas 2.14 1.79 2.09 1.87 2.01
Liquefied gas 10.18 10.94 10.16 10.21 10.45
Gasoline 54.05 50.14 53.18 53.44 53.38
Diesel oil 20.34 22.33 21.71 21.39 20.72
Heavy oil 10.38 12.00 10.78 10.85 11.23
Coke 2.91 2.80 2.08 2.24 2.21
Amount to 100.0 100.0 100.0 100.0 100.0
Transformation efficiency/m% 69.28 65.67 67.51 67.76 68.05
Yield of light oil/m% 74.39 72.47 74.89 74.83 74.10
Light receipts+liquefied gas/m% 84.57 83.40 85.05 85.04 84.55
Heavy oil/coke 3.56 4.28 5.18 4.84 5.08
Coke/transformation efficiency 0.04 0.04 0.03 0.03 0.03
Content of sulfur in gasoline, mg/L 420.93 290.18 260.21 254.50 261.60
Desulfurization degree % base 31.1 38.2 39.5 37.8
By table 5 as seen, contain in the vanadium molecular sieve at desulphurizing activated constituent element and to introduce second metal component and can further improve the desulphurizing activated of catalyzer, the difference of the second metal component introducing amount then causes different desulfurization results.
The desulfurization constituent element is the VAPO-11 that skeleton contains second metal in the catalyzer of embodiment 12~15.
Embodiment 12
Mg-VAPO-11's is synthetic: 15g dry glue powder (Al 2O 3Content 65.8%, the Chang Ling catalyst plant is produced), add water 60mL making beating after 60 minutes to wherein slowly dripping 14g ortho-phosphoric acid solution (phosphorus acid content 85%, Beijing chemical reagent work produces).Stir and add 2.3g five water vanadylic sulfate (V content 22% after 10 minutes, be dissolved in the 2g water), stir after 5 minutes and to add quantitative magnesium chloride solution, continue under the room temperature to stir that the speed with 1mL/min adds 13.6mL template dipropyl amine (content 98%, Beijing chemical reagent work produces) after 60 minutes.Continue to stir after 1 hour, placed 200 ℃ of dynamic crystallizations of crystallizing kettle 96 hours.The X-ray diffraction of products therefrom (XRD) spectrogram has the feature of VAPO-11 molecular sieve, and aluminium vanadium mol ratio is 25, and the magnalium mol ratio is 25.
To synthetic Mg-VAPO-11 as stated above, add the REUSY molecular sieve, aluminium colloidal sol, pseudo-boehmite and kaolin prepare catalyzer with embodiment 1 method, wherein the content of Mg-VAPO-11 is 10 heavy %, REUSY molecular sieve 30 heavy %, aluminium colloidal sol 10 heavy %, pseudo-boehmite 20 heavy % and kaolin 30 heavy %, the spray-dried catalyzer that is prepared into is numbered A10.Evaluation result sees Table 6.
Embodiment 13~15
The catalyzer of embodiment 13~15 is designated as A11 respectively, A12 and A13.
Compare with catalyst A 10, difference is that the magnalium mol ratio is respectively 130,75 and 15 among the used Mg-VAPO-11, and content is respectively 12 heavy %, 6 heavy % and 3 heavy %, and kaolin 28 heavy %, the aluminium sol content is respectively 5 heavy %, 11 heavy % and 13 heavy %.Evaluation result sees Table 6.
Comparative Examples 7
Comparative catalyst DB-7 consists of: VAPO-11 10 heavy %, REUSY molecular sieve 30 heavy %, aluminium colloidal sol 10 heavy %, pseudo-boehmite 20 heavy %, kaolin 30 heavy %.Wherein the preparation method of VAPO-11 does not just wherein add second metallic element with embodiment 12.Evaluation result sees Table 6.
Evaluation result table 6 lists file names with the cracking result of Comparative Examples DB-1 in the table 6.
Table 6
Catalyzer DB-1 DB-7 A10 A11 A12 A13
Al/Mg(mol) 25 130 75 15
MA(800℃/8h) 70 70 70 70 70 70
C/O 1.47 1.47 1.47 1.47 1.47 1.47
Temperature of reaction/℃ 500 500 500 500 500 500
Dry gas 2.14 1.94 2.04 1.87 1.98 2.12
Liquefied gas 10.18 10.87 9.97 10.11 10.69 10.03
Gasoline 54.05 50.97 52.10 52.14 52.07 52.32
Diesel oil 20.34 21.65 21.95 21.58 21.56 21.87
Heavy oil 10.38 11.82 10.89 11.01 10.74 10.93
Coke 2.91 2.75 3.05 3.29 2.96 2.73
Amount to 100.0 100.0 100.0 100.0 100.0 100.0
Transformation efficiency/m% 69.28 66.53 67.16 67.41 67.70 67.20
Yield of light oil/m% 74.39 72.62 74.05 73.72 73.63 74.19
Light receipts+liquefied gas/m% 84.57 83.49 84.02 83.83 84.32 84.22
Heavy oil/coke 3.56 4.29 3.57 3.35 3.63 4.00
Coke/transformation efficiency 0.04 0.04 0.04 0.05 0.04 0.04
Content of sulfur in gasoline, mg/L 420.93 300.14 269.52 266.70 258.60 284.31
Desulfurization degree % base 28.7 36.0 36.6 38.5 32.4
As can be seen from Table 6, A10~A13 compares with not adding the catalyzer DB-1 that contains the vanadium molecular sieve, and the sulphur content of gasoline reduces greatly, and desulfurization degree is all above more than 30%; Compare with only having added the comparative catalyst DB-7 that contains vanadium molecular sieve VAPO-11, transformation efficiency increases, and the sulphur content of gasoline be than can further reducing, and sweetening effectiveness strengthens to some extent.

Claims (12)

1. composition with desulfidation, it is characterized in that said composition mainly is made up of carrier, binding agent, active component and desulfurization constituent element, wherein said active component is the super steady Y or the hyperastable Y-type RE of modified zinc oxide, the desulfurization constituent element is the molecular sieve that contains the v element and the second metallic element M in the skeleton structure, and said second metal M is selected from a kind of in periodic table of elements IIA, IIB, IVB, VIB, VIIB, VIIIB or the lanthanide series rare-earth elements.
2. according to the composition of claim 1, said second metal M is selected from Be, Mg, Ti, Mn, Zn, Fe, Cr, Co or Ce.
3. according to the composition of claim 1, the molecular sieve that contains the v element and the second metallic element M in the said skeleton structure accounts for 1~20 heavy %.
4. according to the composition of claim 3, the molecular sieve that contains the v element and the second metallic element M in the said skeleton structure accounts for 7~15 heavy %.
5. according to the composition of claim 1, the ratio that contains the molecular sieve of the v element and the second metallic element M in said active component and the skeleton structure is 1~50.
6. according to the composition of claim 5, the ratio that contains the molecular sieve of the v element and the second metallic element M in said active component and the skeleton structure is 3~20.
7. according to the composition of claim 1, one or more the mixture of the molecular screening that contains the v element and the second metallic element M in the said skeleton structure in vanadium metal si molecular sieves, metal tripolyphosphate vanadium aluminum molecular screen and metal tripolyphosphate vanadium Si-Al molecular sieve.
8. according to the composition of claim 7, said metal tripolyphosphate vanadium aluminum molecular screen is VAPO-5, VAPO-11, VAPO-17 or VAPO-31, and the mol ratio of aluminium and vanadium is 10~300.
9. according to the composition of claim 1, said carrier is a kaolin.
10. according to the composition of claim 1, said binding agent is selected from a kind of in silicon sol, aluminium colloidal sol and the pseudo-boehmite or two kinds or three's mixture wherein.
11. a process that reduces content of sulphur compounds is characterized in that this process is to carry out in the presence of the composition of claim 1.
12. a catalytic cracking reaction method is characterized in that this method is to react in the presence of the said composition of claim 1.
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CN102389791A (en) * 2011-09-22 2012-03-28 大连理工大学 Desulfurization and denitrification catalyst taking kaolin as carrier and preparation method thereof
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CN106582252B (en) * 2016-12-21 2020-04-24 贵州大学 Flue gas desulfurization and mercury removal agent and preparation method thereof

Citations (2)

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CN1011960B (en) * 1984-04-13 1991-03-13 联合碳化公司 The preparation method of combination of molecular sieve
CN1261618A (en) * 1998-12-28 2000-08-02 美孚石油公司 Gasoline desulfating method in fluidized catalyst cracking process

Patent Citations (2)

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Publication number Priority date Publication date Assignee Title
CN1011960B (en) * 1984-04-13 1991-03-13 联合碳化公司 The preparation method of combination of molecular sieve
CN1261618A (en) * 1998-12-28 2000-08-02 美孚石油公司 Gasoline desulfating method in fluidized catalyst cracking process

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