CN100548478C - A kind of catalyst and method for making and application by the synthesis gas synthesizing methanol - Google Patents
A kind of catalyst and method for making and application by the synthesis gas synthesizing methanol Download PDFInfo
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- CN100548478C CN100548478C CNB2006101022291A CN200610102229A CN100548478C CN 100548478 C CN100548478 C CN 100548478C CN B2006101022291 A CNB2006101022291 A CN B2006101022291A CN 200610102229 A CN200610102229 A CN 200610102229A CN 100548478 C CN100548478 C CN 100548478C
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Abstract
A kind of percentage by weight of the catalyst by the synthesis gas synthesizing methanol consists of CuO:40～60%, ZnO:30～50%, Al
2O
3: 3～7%, SiO
2, WO
3, HAlO
2In one or more: 3～7%.Adopt prepared by co-precipitation catalyst of the present invention, the present invention has because modified component is participated in the precipitation reaction of CuZnAl directly, forms Siization thing, Wization thing, the Alization thing of CuZnAl, has intercepted the gathering of Cu, has prolonged the advantage of life of catalyst.
Description
Technical field
The present invention relates to a kind of catalyst for methanol and preparation method and application, relate in particular to a kind of catalyst and preparation method and application by the synthesis gas synthesizing methanol.
Background technology
Along with the increase for the Imported oil interdependency of high and China of International Crude Oil, according to the abundant specific national conditions of coal in China, it is imperative that exploitation is produced high-quality gasoline from coal.This process might form industry series and new and high technology engineering rapidly, becomes new growth engines, has guaranteed the energy security of China and the sustainable development of national economy.Coal system oil finds that from Fischer and the Tropsch of nineteen twenty-three synthesis gas generates liquid hydrocarbon through catalytic reaction and counts, and has experienced 80 years of development courses.Say from reaction mechanism, mainly contain two aspects: one is to transform or be reformatted into gasoline again from the direct Synthin of synthesis gas, i.e. F-T or improvement F-T method; Another is from synthesis gas through methanol, dimethyl ether synthetic gasoline, i.e. MTG and improvement MTG method.In the synthetic oil product of F-T, the carbon number distribution broad especially is fit to combined diesel oil.The MTG artificial oil is through methyl alcohol, dimethyl ether process, and in the hydrocarbon product of methyl alcohol, dimethyl ether dehydration generation, the overwhelming majority (more than 75%) is C
5-C
11 +Gasoline fraction, be suitable for gasoline production.Existing improvement MTG process mainly contains the Tigas process of Denmark Tops Φ e company exploitation and the AMSTG process of MIT's exploitation.These two kinds of methods all rest on the pilot scale stage at present.China's research in this regard also is in the starting stage.
One section catalyst that coal based synthetic gas uses in the process of methanol and dimethyl ether system gasoline generates the composite catalyst of the dehydration catalyst composition of dimethyl ether as catalyst for synthesizing copper based methanol and methanol dehydration.Independent methanol synthesis catalyst and methanol dehydration catalyst all have preferably stability, but they mix the composite catalyst of composition and just have the characteristics of poor stability.Both at home and abroad result of study is in this regard thought the main cause (Jia Meilin of composite catalyst inactivation, Xu Hengyong, Li Wenzhao etc., Journal of Molecular Catalysis, 2004,18 (5): 351-356) be not catalyst surface acidity, catalyst surface adsorbing species and area carbon, but catalyst in use active component Cu sintering cause the reduction of Cu specific area; The existence of water and rich methanol liquid phase has promoted growing up of Cu/Zn/Al catalyst crystal grain to cause catalysqt deactivation (Gogate M R, Foos A, Lee S, et al.Fuel Sci Technol.Int, 1991,9 (8): 653-679) in the slurry attitude bed; In the slurry attitude bed methanol synthesis catalyst in the increase of active component Cu crystal grain and the methanol synthesis catalyst Cu element run off and cause catalyst activity to reduce (Liu Hongwei, Nie Zhaoguang, Liu Dianhua etc., East China University of Science's journal: natural science edition, 2006,32 (4): 365-369,380) cause catalysqt deactivation; The inactivation of slurry attitude bed composite catalyst mainly be since the inactivation of methanol synthesis catalyst cause (Ma Hongbin, Jia Guangxin, Tan petrochemical industry, 2004,33 (7): 612-614) etc. such as give birth to.As seen, the inactivation of coal based synthetic gas one section catalyst in methyl alcohol, dimethyl ether system gasoline process mainly is the inactivation of methanol synthesis catalyst.Therefore, the preparation of catalyst for methanol will have influence on life of catalyst.The preparation method of existing catalyst for methanol mostly adopts carbonate, ammoniacal liquor to make precipitating reagent, as: Deutsche Bundespatent DD296855, Canadian Patent CA1011325 disclose a kind of technology of preparing of catalst for synthesis of methanol, are the aqueous solution and alkali carbonate prepared by co-precipitation catalyst with the soluble-salt of copper, zinc, aluminium; Chinese patent CN1131102C has announced a kind of preparation method of catalyst for methanol, is the mixed solution of Cu/Zn/Al is mixed with acid carbonate solution, makes high-activity mother body; Chinese patent CN1176747C points out a kind of preparation method of Cu-series catalyst carrier for synthesizing methanol, prepares catalyst for methanol with the ammoniacal liquor of 0.5-20% as precipitating reagent, and more than Zhi Bei catalyst life is shorter.
Summary of the invention:
The object of the invention provides long catalyst and method for making and methods for using them by the synthesis gas synthesizing methanol of a kind of life-span.
Catalyst weight percentage of the present invention is formed
CuO：40～60％ ZnO：30～50％ Al
2O
3：3～7％
SiO
2, WO
3, HAlO
2In one or more: 3～7%
Preparation method of the present invention comprises the steps:
Cu (NO
3)
23H
2O, Zn (NO
3)
26H
2O and Al (NO
3)
39H
2O is mixed with the aqueous solution of 0.5-1.0M respectively, and the composition of pressing catalyst mixes, and counts A liquid; Wherein one or more of sodium metasilicate, sodium tungstate, sodium aluminate are made into the aqueous solution of 0.5-1.0M, count B liquid; Anhydrous Na
2CO
3Be mixed with the aqueous solution of 0.5-1.0M, count C liquid.
Adding and A liquid volume ratio are 1: 3～1: 5 distilled water in the reactor, and be heated to 50～70 ℃, A, B solution presses the catalyst composition and stream is introduced in the reactor, simultaneously C solution is added the pH value of solution value that makes in the reactor in the reactor between 6～10, the beginning co-precipitation, the sediment suction filtration that obtains, washing does not detect to there being the sodium particle, with the moisture in the absolute ethyl alcohol displacement filter cake, until water content less than 0.1wt%, the anhydrous filter cake that obtains is ℃ following drying in room temperature～50,300～500 ℃ of roastings of Muffle furnace 3～7 hours, be crushed to below 250 orders then, make catalyst for methanol.
Dehydration catalyst is that weight percentage is CuO:20～40%, ZnO:5～30%, La
2O
3: 1～10%, Sm
2O
3: 1～10%, V
2O
5: 1～10%, carrier: 40～60% catalyst.The preparation method is dissolved in copper nitrate or Schweinfurt green, zinc nitrate or zinc acetate, lanthanum nitrate in the solvent with the ratio of 1.2～2ml solvent/g carrier in the composition of catalyst, adds carrier, stirs; Form by catalyst then and add the Sm that is ground into below 250 orders again
2O
3, V
2O
5, continue to stir, dry 60～100 ℃ of following infrared lamp irradiations, 350～500 ℃ of roastings are crushed to below 250 orders, make dehydration catalyst, and concrete preparation method sees patent CN1745894A.
With the catalyst for methanol of above preparation and dehydration catalyst is that 1～4: 1 ratio is mixed by weight, in the slurry attitude of packing into the bed bubbling column reactor, at H
2: CO=1～4: 1,260～300 ℃, 3～7MPa, 50000～150000h
-1Condition under carry out synthetic reaction.
Advantage of the present invention:
Active component adds by anionic form among the present invention.Because modified component is participated in the precipitation reaction of CuZnAl directly, form Siization thing, Wization thing, the Alization thing of CuZnAl, intercepted the gathering of Cu, prolonged life of catalyst.
The specific embodiment:
Comparative Examples:
121.4 gram Cu (NO
3)
23H
2O, 182.8 gram Zn (NO
3)
26H
2O and 73.6 gram Al (NO
3)
39H
2O is mixed with the aqueous solution of 1.0M respectively, forms mixed liquor and counts A liquid; Anhydrous Na
2CO
3Be made into the aqueous solution of 1.0M, count B liquid.
Adding in the reactor with A liquid volume ratio is 1: 4 distilled water, adds hot water to 60 ℃.A, B two liquid are introduced reactor simultaneously, regulate pH value=8 of precipitated liquid, the beginning co-precipitation.The sediment suction filtration that obtains, washing do not detect to there being the sodium particle, with the moisture in the absolute ethyl alcohol displacement filter cake.The suction filtration liquid that displaces is carried out chromatography, to water content less than 0.1% (wt.).The anhydrous filter cake natural air drying that obtains 400 ℃ of roastings of Muffle furnace 5 hours, is crushed to below 250 orders then, makes CuO: ZnO: Al
2O
3Weight percentage is 40: 50: 10 a catalyst for methanol.
Dehydration catalyst (CN1745894) is that weight percentage is: CuO:20, ZnO:20, La
2O
3: 6, Sm
2O
3: 6, V
2O
5: 8, SiO
2: 40 catalyst.Concrete preparation method is nitrate trihydrate copper 60.7g, zinc nitrate hexahydrate 73.1g, and lanthanum nitrate hexahydrate 15.6g is dissolved in slaine in butanols+ethanol with the ratio of 1.8ml solvent/g carrier, pours 40g carrier S iO into
2, stir.And then add the samarium oxide 6g that is ground into below 250 orders, and vanadic anhydride 8g continues to stir, and 80 ℃ of infrared lamps irradiations are dry, and 450 ℃ of roastings are crushed to below 250, make dehydration catalyst.The above catalyst that makes is mixed with the weight ratio of catalyst for methanol/dehydration catalyst (wt.)=2, be contained in the slurry attitude bed bubbling column reactor.At H
2: CO=2,280 ℃, 5MPa, 80000h
-1, condition under, CO conversion ratio (mol) reduces to 25.4% 300 hours running backs by 58.5%.
Embodiment 1:
182.0 gram Cu (NO
3)
23H
2O, 109.7 gram Zn (NO
3)
26H
2O and 36.8 gram Al (NO
3)
39H
2O is mixed with the aqueous solution of 0.5M respectively, forms mixed liquor and counts A liquid; 23.6 gram Na
2SiO
39H
2O is mixed with the aqueous solution of 0.5M, counts B liquid; Anhydrous Na
2CO
3Be mixed with the aqueous solution of 0.5M, count C liquid.
It is 1: 3 distilled water that reactor adds with A liquid volume ratio, adds hot water to 50 ℃.Two kinds of liquid of A, B are introduced reactor simultaneously, add C liquid simultaneously, to regulate pH value=10 of precipitated liquid, the beginning co-precipitation.The sediment suction filtration that obtains, washing do not detect to there being the sodium particle, with the moisture in the absolute ethyl alcohol displacement filter cake.The suction filtration liquid that displaces is carried out chromatography, to water content less than 0.1% (wt.).50 ℃ of dryings of the anhydrous filter cake that obtains 300 ℃ of roastings of Muffle furnace 7 hours, are crushed to below 250 orders then, make CuO: ZnO: Al
2O
3: SiO
2Weight percentage is 60: 30: 5: 5 catalyst for methanol.
Dehydration catalyst (CN1745894) is that weight percentage is: CuO:20, ZnO:20, La
2O
3: 6, Sm
2O
3: 6, V
2O
5: 8, SiO
2: 40 catalyst.Concrete preparation method is nitrate trihydrate copper 60.7g, zinc nitrate hexahydrate 73.1g, and lanthanum nitrate hexahydrate 15.6g is dissolved in slaine in butanols+ethanol with the ratio of 1.8ml solvent/g carrier, pours 40g carrier S iO into
2, stir.And then add the samarium oxide 6g that is ground into below 250 orders, and vanadic anhydride 8g continues to stir, and 80 ℃ of infrared lamps irradiations are dry, and 450 ℃ of roastings are crushed to below 250, make dehydration catalyst.
The ratio of the above catalyst that makes with catalyst for methanol/dehydration catalyst (wt.)=4 mixed the slurry attitude of packing into bed bubbling column reactor.At H
2: CO=1,300 ℃, 7Mpa, 150000h
-1, condition under, CO conversion ratio (mol) reduces to 54.8% 300 hours running backs by 65.6%.
Embodiment 2:
151.7 gram Cu (NO
3)
23H
2O, 146.2 gram Zn (NO
3)
26H
2O and 51.5 gram Al (NO
3)
39H
2O is mixed with the aqueous solution of 0.7M respectively, forms mixed liquor and counts A liquid; 4.3 gram Na
2WO
42H
2O is mixed with the aqueous solution of 0.7M, counts B liquid; Anhydrous Na
2CO
3Be mixed with the aqueous solution of 0.7M, count C liquid.
Adding in the reactor with A liquid volume ratio is 1: 5 distilled water, adds hot water to 70 ℃.Two kinds of liquid of A, B are introduced reactor, add C liquid simultaneously, to regulate pH value=6 of precipitated liquid, the beginning co-precipitation.The sediment suction filtration that obtains, washing do not detect to there being the sodium particle, with the moisture in the absolute ethyl alcohol displacement filter cake.The suction filtration liquid that displaces is carried out chromatography, to water content less than 0.1% (wt.).40 ℃ of the anhydrous filter cakes that obtains 500 ℃ of roastings of Muffle furnace 3 hours, are crushed to below 250 orders then, make CuO: ZnO: Al
2O
3: WO
3Weight percentage is 50: 40: 7: 3 catalyst for methanol.
Dehydration catalyst (CN1745894) is that weight percentage is: CuO:20, ZnO:5, La
2O
3: 5, Sm
2O
3: 5, V
2O
5: 5, the catalyst of HZSM-5:60.Concrete preparation method is nitrate trihydrate copper 60.7g, zinc nitrate hexahydrate 18.3g, and lanthanum nitrate hexahydrate 13.3g is dissolved in slaine in propyl alcohol+butanols+ethanol with the ratio of 1.8ml solvent/g carrier, pours 60g carrier HZSM-5 into, stirs.And then add the samarium oxide 5g that is ground into below 250 orders, and vanadic anhydride 5g continues to stir, and 70 ℃ of infrared lamps irradiations are dry, and 450 ℃ of roastings are crushed to below 250, make dehydration catalyst.
With the above catalyst that makes with catalyst for methanol: the ratio of dehydration catalyst (wt.)=1 is mixed, the slurry attitude of packing into bed bubbling column reactor.At H
2: CO=4,260 ℃, 3Mpa, 50000h
-1, condition under, CO conversion ratio (mol) reduces to 38.8% 300 hours running backs by 54.5%.
Embodiment 3:
121.4 gram Cu (NO
3)
23H
2O, 182.8 gram Zn (NO
3)
26H
2O and 22.1 gram Al (NO
3)
39H
2O is mixed with the aqueous solution of 1M respectively, forms mixed liquor and counts A liquid; 23.6 gram Na
2SiO
39H
2O, 2.8 gram Na
2WO
42H
2O is mixed with the aqueous solution of 1M respectively, forms mixed liquor and counts B liquid; Anhydrous Na
2CO
3Be mixed with the solution of 1M, count C liquid.
Adding in the reactor with A liquid volume ratio is 1: 4 distilled water, adds hot water to 60 ℃.Two kinds of liquid of A, B are introduced reactor, add C liquid simultaneously, in order to regulate the pH=8 of precipitated liquid, the beginning co-precipitation.The sediment suction filtration that obtains, washing do not detect to there being the sodium particle, with the moisture in the absolute ethyl alcohol displacement filter cake.The suction filtration liquid that displaces is carried out chromatography, to water content less than 0.1% (wt.).35 ℃ of dryings of the anhydrous filter cake that obtains 400 ℃ of roastings of Muffle furnace 3 hours, are crushed to below 250 orders then, make CuO: ZnO: Al
2O
3: SiO
2: WO
3Weight percentage is 40: 50: 3: 5: 2 catalyst for methanol.
Dehydration catalyst (CN1745894) is that weight percentage is: CuO:20, ZnO:10, La
2O
3: 10, Sm
2O
3: 10, V
2O
5: 10, SiO
2: 20, Al
2O
3: 20 catalyst.Concrete preparation method is nitrate trihydrate copper 60.7g, zinc acetate dihydrate 27g, and lanthanum nitrate hexahydrate 26.6g is dissolved in slaine in the ethanol with the ratio of 1.8ml solvent/g carrier, pours carrier 20g SiO into
2, 20gAl
2O
3, stir.And then add the samarium oxide 10g that is ground into below 250 orders, and vanadic anhydride 10g continues to stir, and 90 ℃ of infrared lamps irradiations are dry, and 500 ℃ of roastings are crushed to below 250, make dehydration catalyst.
The above catalyst that makes is mixed with the ratio of catalyst for methanol/dehydration catalyst (wt.)=2, in the slurry attitude of packing into the bed bubbling column reactor.At H
2: CO=2,280 ℃, 5Mpa, 80000h
-1, condition under, CO conversion ratio (mol) reduces to 51.9% 300 hours running backs by 60.8%.
Embodiment 4:
121.4 gram Cu (NO
3)
23H
2O, 182.8 gram Zn (NO
3)
26H
2O and 22.1 gram Al (NO
3)
39H
2O is mixed with the aqueous solution of 1M respectively, forms mixed liquor and counts A liquid; 4.1 gram NaAlO
2, 5.7 the gram Na
2WO
42H
2O is mixed with the aqueous solution of 1M respectively, forms mixed liquor and counts B liquid; Anhydrous Na
2CO
3Be mixed with the solution of 1M, count C liquid.
Adding in the reactor with A liquid volume ratio is 1: 4 distilled water, adds hot water to 60 ℃.Two kinds of liquid of A, B are introduced reactor, add C liquid simultaneously, regulate the pH=8 of precipitated liquid, the beginning co-precipitation.The sediment suction filtration that obtains, washing do not detect to there being the sodium particle, with the moisture in the absolute ethyl alcohol displacement filter cake.The suction filtration liquid that displaces is carried out chromatography, to water content less than 0.1% (wt.).40 ℃ of dryings of the anhydrous filter cake that obtains 400 ℃ of roastings of Muffle furnace 3 hours, are crushed to below 250 orders then, make CuO: ZnO: Al
2O
3: WO
3: HAlO
2Weight percentage is 40: 50: 3: 4: 3 catalyst for methanol.
Dehydration catalyst (CN1745894) is that weight percentage is: CuO:30, ZnO:10, La
2O
3: 10, Sm
2O
3: 5, V
2O
5: 5, SiO
2: 20, the catalyst of HZSM-5:20.Concrete preparation method is a water acetic acid copper 75.2g, six water acetic acid zinc 36.5g, and lanthanum nitrate hexahydrate 26.6g is dissolved in slaine in the ethanol with the ratio of 1.5ml solvent/g carrier, pours carrier 20gSiO into
2, 20gHZSM-5, stir.And then add the samarium oxide 5g that is ground into below 250 orders, and vanadic anhydride 5g continues to stir, and 80 ℃ of infrared lamps irradiations are dry, and 350 ℃ of roastings are crushed to below 250, make dehydration catalyst.
The above catalyst that makes is mixed the slurry attitude of packing into bed bubbling column reactor with the ratio of catalyst for methanol/dehydration catalyst (wt.)=2.At H
2: CO=2,280 ℃, 5Mpa, 80000h
-1, under the condition, CO conversion ratio (mol) reduces to 54.3% 300 hours running backs by 62.7%.
Embodiment 5:
121.4 gram Cu (NO
3)
23H
2O, 182.8 gram Zn (NO
3)
26H
2O and 22.1 gram Al (NO
3)
39H
2O is mixed with the aqueous solution of 1M respectively, forms mixed liquor and counts A liquid; 9.6 gram NaAlO
2Be mixed with the aqueous solution of 1M, count B liquid; Anhydrous Na
2CO
3Be made into the solution of 1M, count C liquid.
Adding in the reactor with A liquid volume ratio is 1: 4 distilled water, adds hot water to 60 ℃.Two kinds of liquid of A, B are introduced reactor, add C liquid simultaneously, the pH=8 of regulator solution, beginning co-precipitation.The sediment suction filtration that obtains, washing do not detect to there being the sodium particle, with the moisture in the absolute ethyl alcohol displacement filter cake.The suction filtration liquid that displaces is carried out chromatography, to water content less than 0.1% (wt.).50 ℃ of dryings of the anhydrous filter cake that obtains 400 ℃ of roastings of Muffle furnace 3 hours, are crushed to below 250 orders then, make CuO: ZnO: Al
2O
3: HAlO
2Weight percentage is 40: 50: 3: 7 catalyst for methanol.
Dehydration catalyst (CN1745894) is that weight percentage is: CuO:20, ZnO:30, La
2O
3: 1, Sm
2O
3: 1, V
2O
5: 1, Al
2O
3: 47 catalyst.Concrete preparation method is nitrate trihydrate copper 60.7g, six water acetic acid zinc 109.6g, and lanthanum nitrate hexahydrate 2.7g is dissolved in slaine in methyl alcohol+ethanol+acetone with the ratio of 2ml solvent/g carrier, pours carrier 47g carrier A l into
2O
3, stir.And then add the samarium oxide 1g that is ground into below 250 orders, and vanadic anhydride 1g continues to stir, and 100 ℃ of infrared lamps irradiations are dry, and 450 ℃ of roastings are crushed to below 250, make dehydration catalyst.
The above catalyst that makes is mixed with the ratio of catalyst for methanol/dehydration catalyst (wt.)=2, in the slurry attitude of packing into the bed bubbling column reactor.At H
2: CO=2,280 ℃, 5Mpa, 80000h
-1, under the part, CO conversion ratio (mol) reduces to 49.5% 300 hours running backs by 60.0%.
Embodiment 6:
121.4 gram Cu (NO
3)
23H
2O, 182.8 gram Zn (NO
3)
26H
2O and 22.1 gram Al (NO
3)
39H
2O is mixed with the aqueous solution of 1M respectively, forms mixed liquor and counts A liquid; 9.5 gram Na
2SiO
39H
2O, 6.8 gram NaAlO
2Be mixed with the aqueous solution of 1M respectively, form mixed liquor and count B liquid; Anhydrous Na
2CO
3Be made into the solution of 1M.
Adding in the reactor with A liquid volume ratio is 1: 4 distilled water, adds hot water to 60 ℃.Two kinds of liquid of A, B are introduced reactor, add C liquid simultaneously, the pH=8 of regulator solution, beginning co-precipitation.The sediment suction filtration that obtains, washing do not detect to there being the sodium particle, with the moisture in the absolute ethyl alcohol displacement filter cake.The suction filtration liquid that displaces is carried out chromatography, to water content less than 0.1% (wt.).The anhydrous filter cake natural air drying that obtains 400 ℃ of roastings of Muffle furnace 3 hours, is crushed to below 250 orders then, makes CuO: ZnO: Al
2O
3: SiO
2: HAlO
2Weight percentage is 40: 50: 3: 2: 5 catalyst for methanol.
Dehydration catalyst (CN1745894) is that weight percentage is: CuO:40, ZnO:5, La
2O
3: 5, Sm
2O
3: 5, V
2O
5: 5, Al
2O
3: 40 catalyst.Concrete preparation method is nitrate trihydrate copper 121.4g, six water acetic acid zinc 18.3g, and lanthanum nitrate hexahydrate 13.3g is dissolved in slaine in methyl alcohol+acetone with the ratio of 1.3ml solvent/g carrier, pours carrier 40g Al into
2O
3, stir.And then add the samarium oxide 5g that is ground into below 250 orders, and vanadic anhydride 5g continues to stir, and 60 ℃ of infrared lamps irradiations are dry, and 350 ℃ of roastings are crushed to below 250, make dehydration catalyst.
The above catalyst that makes is mixed with the ratio of catalyst for methanol/dehydration catalyst (wt.)=2, in the slurry attitude of packing into the bed bubbling column reactor.At H
2: CO=2,280 ℃, 5Mpa, 80000h
-1, condition under, CO conversion ratio (mol) reduces to 51.5% 300 hours running backs by 56.3%.
Claims (3)
1, a kind of catalyst by the synthesis gas synthesizing methanol is characterized in that catalyst weight percentage composition:
CuO：40～60％ ZnO：30～50％ Al
2O
3：3～7％
WO
3Or HAlO
2: 3～7%;
2, a kind of Preparation of catalysts method by the synthesis gas synthesizing methanol as claimed in claim 1 is characterized in that comprising the steps:
Cu (NO
3)
23H
2O, Zn (NO
3)
26H
2O and Al (NO
3)
39H
2O is mixed with the aqueous solution of 0.5-1.0M respectively, and the composition of pressing catalyst mixes, and counts A liquid; Sodium tungstate or sodium aluminate are made into the aqueous solution of 0.5-1.0M, count B liquid; Anhydrous Na
2CO
3Be mixed with the aqueous solution of 0.5-1.0M, count C liquid;
Adding and A liquid volume ratio are 1: 3～1: 5 distilled water in the reactor, and be heated to 50～70 ℃, A, B solution presses the catalyst composition and stream is introduced in the reactor, simultaneously C solution is added the pH value of solution value that makes in the reactor in the reactor between 6～10, the beginning co-precipitation, the sediment suction filtration that obtains, washing does not detect to there being the sodium particle, with the moisture in the absolute ethyl alcohol displacement filter cake, until water content less than 0.1wt%, the anhydrous filter cake that obtains is ℃ following drying in room temperature～50,300～500 ℃ of roastings of Muffle furnace 3～7 hours, be crushed to below 250 orders then, make described catalyst.
3, a kind of Application of Catalyst by the synthesis gas synthesizing methanol as claimed in claim 1 is characterized in that comprising the steps:
Described catalyst and dehydration catalyst are that 1～4: 1 ratio is mixed by weight, in the slurry attitude of packing into the bed bubbling column reactor, at H
2: CO=1～4: 1,260～300 ℃, 3～7MPa, 50000～150000h
-1Condition under carry out synthetic reaction;
Described dehydration catalyst is that weight percentage is CuO:20～40%, ZnO:5～30%, La
2O
3: 1～10%, Sm
2O
3: 1～10%, V
2O
5: 1～10%, carrier: 40～60% catalyst.
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN101306369B (en) * | 2008-07-11 | 2010-04-14 | 西南化工研究设计院 | Catalyst for synthesizing methanol and preparing process thereof |
| CN101322940B (en) * | 2008-07-23 | 2010-06-02 | 大连瑞克科技有限公司 | Catalyst for synthesizing methanol and preparation thereof |
| CN101983765B (en) * | 2010-11-15 | 2012-12-26 | 大连理工大学 | Catalyst for preparing methyl alcohol by catalytic hydrogenation on assistant modified carbon dioxide and preparation method thereof |
| CN103466727A (en) * | 2012-06-08 | 2013-12-25 | 中国石油化工股份有限公司 | Method for reducing content of impurity ions introduced during preparation of oxides |
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