CN108640824A - A kind of method that catalysis oxidation benzyl alcohol prepares benzaldehyde - Google Patents

A kind of method that catalysis oxidation benzyl alcohol prepares benzaldehyde Download PDF

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CN108640824A
CN108640824A CN201810349635.0A CN201810349635A CN108640824A CN 108640824 A CN108640824 A CN 108640824A CN 201810349635 A CN201810349635 A CN 201810349635A CN 108640824 A CN108640824 A CN 108640824A
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benzyl alcohol
catalyst
catalysis oxidation
benzaldehyde
temperature
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王飞利
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Foshan Flying Information Technology Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/37Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups
    • C07C45/38Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups being a primary hydroxyl group
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/76Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/80Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with zinc, cadmium or mercury
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/584Recycling of catalysts

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  • Organic Chemistry (AREA)
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Abstract

The present invention relates to a kind of methods that catalysis oxidation benzyl alcohol prepares benzaldehyde, and using xCu-yZn/CNTS catalyst, wherein the x is the mass percentage of Ni metal in the catalyst, x is 0.01%~20%;The y is the mass percentages of metal Zn in the catalyst, and y is 0.1%~30%;The catalyst has good temperature tolerance, within the scope of very wide temperature (220 DEG C~400 DEG C), has stable catalytic performance, the stable structure in gas phase successive reaction, service life length and easily-activated regeneration.

Description

A kind of method that catalysis oxidation benzyl alcohol prepares benzaldehyde
Technical field
The invention belongs to field of fine chemical more particularly to a kind of methods that catalysis oxidation benzyl alcohol prepares benzaldehyde.
Background technology
Benzaldehyde is important organic intermediate, can be used for the industries such as medicine, fragrance, dyestuff, food and pesticide, at present work Industry preparation method mainly has subsegment base dichloro Hydrolyze method, toluene gas phase, liquid phase oxidation to save alcohol oxidizing process, toluene Indirect Electro oxygen Change method and benzoic acid or its vinegar reduction method.
The application of benzal chloride Hydrolyze method is relatively wide, in particular to toluene is carried out pendant chlorine under proper condition, obtains Benzal chloride, then benzal chloride is hydrolyzed under acid or alkaline conditions, benzene first can be obtained by finally carrying out rectifying to hydrolyzate Aldehyde, by-product are benzoic acid, and this method advantage is that reaction is simple, and technical maturity, the disadvantage is that reaction step is more, yield is not high, corrosion Seriously polluted, three waste discharge is more, does not meet Atom economy.
The vapour phase oxidation process of toluene often makees catalyst with the oxide of the transition metal such as vanadium, key, uranium, iron, using fixed bed Technique makees oxidant with air or oxygen, is reacted to prepare benzaldehyde, instead under the conditions of high temperature (350~550 DEG C), high-speed Answer conversion ratio insufficient, selectivity is less than 80%.According to Wu Zebiao et al., fixed-bed process is replaced using membrane reactor, it can be big Big to improve conversion ratio, for high conversion rate up to 19%, selectivity is 79%.
Benzaldehyde " green " production technology has toluene oxidation method, reduction method and benzyl alcohol direct oxidation method etc..Wherein toluene Oxidizing process is low since there are product yields, and the defect more than by-product limits its industrial applications, and reduction method is due to adding hydrogen also Former technique productions cost is excessively high without the market competitiveness.Benzyl alcohol direct oxidation method, due to simple for process, environment friend Good feature and show good application prospect.Benzyl alcohol direct oxidation method can be divided into two kinds according to the difference of operation temperature, One is gaseous oxidation methods and liquid oxidatively method.The reaction temperature that vapour phase oxidation process requires is higher, and many catalyst are in 300 DEG C of With relatively good catalytic activity, and vapour phase oxidation process needs special fixed bed reactors, these are all unfavorable for this method Heavy industrialization application.Benzyl alcohol liquid phase oxidation depends on the development of catalyst, and technics comparing is simple, reacts item Part is mild, some catalyst also show relatively good catalytic activity at 90 DEG C.At present benzyl alcohol liquid phase oxidation research compared with More catalyst mainly has loaded noble metal catalyst, non-noble metal oxide catalyst, heteropoly acid and its supported catalyst Agent, ionic liquid catalyst systems and carrier-borne transition metal organic complex catalyst.Such as with 3- aminopropyl-triethoxy silicon Alkane is modified carrier TiO2, as a result, it has been found that:Under identical preparation condition and identical reaction condition, before functionalization The conversion ratio of the corresponding benzyl alcohol of Pd/TiO2 catalyst be 57.6%, selectivity is 74.1%, and the Pd/ after functionalization TiO2 catalyst, the conversion ratio of benzyl alcohol are 61.5, and benzaldehyde selectively reaches 81.4, the conversion ratio of catalyst before and after functionalization It all increases with selectivity.By-product is relatively more on the whole for this kind of catalyst, and the separation of product is more complicated.In addition it crosses Crossing metal (Cu, Pd, Ru etc.) complex compound catalyst has the activity and selectivity of higher benzyl alcohol selective oxidation producing benzaldehyde, But in practical applications, such catalyst still have catalyst and product separation are difficult, catalyst is of high cost, catalyst easily from The problems such as reuniting and inactivating.
In recent years, using molecular oxygen as oxidant, using solid catalyst, fixed bed reactors, gas-solid phase selectivity are utilized Catalysis oxidation benzyl alcohol generates benzaldehyde, since reaction process is solvent-free, by-product is few, product is easily separated, catalyst reprocessing Relatively simple and successive reaction is easy to industrialized production, and reaction process is environmentally protective and receives favor.
Temperature is to influence an important factor for benzyl alcohol gas phase selective catalytic oxidation reaction prepares benzaldehyde, and temperature increases meeting Cause target product benzaldehyde peroxidating to generate benzoic acid, target product selectivity is made to decline, by-product increases, and high temperature is anti- It answers, energy consumption increases, and security risk increases, and is unfavorable for energy conservation and environmental protection and safety in production, does not meet the strategy of sustainable development.In recent years Come, low-temperature gaseous phase selective catalytic oxidation benzyl alcohol generates benzaldehyde, and reaction temperature is low, not only contributes to improve purpose product choosing Selecting property improves the service life of active sites, and energy conservation and environmental protection, and people is caused more and more to pay attention to.
Ag base supported catalysts since preparation method is simple, active component high degree of dispersion, activity is high, selectivity is strong and Have many advantages, such as that higher active surface area, price are significantly reduced compared with Au base catalyst, is widely used in dimethyl oxalate and adds The oxidation of hydrogen synthesizing methyl glycolate, formaldehyde is eliminated, the selective oxidation of alkyl-substituted aromatic hydrocarbon synthesizes ketone, aldehydes-alkynes-amine In the reactions such as the tri compound reaction of class compound, CO oxidations, benzyl alcohol selective preparing benzaldehyde by oxidizing, and show very well Catalytic performance.
Tsuruya et al. (JournalofCatalysis, 2005,234:308-317) Ag is carried on using infusion process On SiO2, and use it in the reaction of benzyl alcohol catalytic gas phase oxidation producing benzaldehyde.As a result, it has been found that Ag/SiO2 catalyst pair Benzyl alcohol gas phase oxidation has preferable catalytic activity.When reaction temperature is 320 DEG C, benzaldehyde yield is 80%, selection Property is close to 100%.But reaction temperature is far above the vapourizing temperature of benzyl alcohol.
Sawayama et al. (IndEngChemRes, 2006,45:Ag loaded catalysts 8837-8845) are reported to exist Application in catalytic gas phase oxidation benzyl alcohol producing benzaldehyde.Author has synthesized different carriers (SiO2/ with infusion process in the literature CaO Ag supported catalysts), and K/Ag/SiO2 catalyst on this basis.System thinking catalyst calcination temperature, The influence of reaction time and reaction temperature to catalyst activity.Reaction yield is up to 84.2%.Although catalyst compared with It is very high to the selectivity of benzaldehyde under low temperature, but conversion ratio is unsatisfactory.
A kind of catalyst and preparation method thereof for low-temperature gaseous phase synthesis of benzaldehyde is disclosed in CN102139224A, with M-Ag-HMS (M is alkali metal, alkaline-earth metal or thulium) is catalyst, reaction temperature at 215 DEG C~220 DEG C, The conversion ratio of benzyl alcohol reaches 94.71%, and the selectivity of benzaldehyde is 97.56%.However the tolerance of the temperature of catalyst compared with Difference, when reaction temperature is 320 DEG C, the conversion ratio of benzyl alcohol drops to 64.11%, and the selectivity of benzaldehyde is 95.53%.Ma etc. People (ChineseJournalofCatalysis, 2013) is prepared for Ag/SBA-15 with infusion process, and is selected for benzyl alcohol gas phase Oxidative synthesis benzaldehyde is selected, when reaction temperature is 240 DEG C, conversion ratio and selectivity reach 94% or more, due to reaction process Reunion, loss and the carbon deposit of middle Ag causes its service life shorter.
In conclusion be currently used for gas phase selective catalytic oxidation alcohol prepare corresponding aldehydes or ketones catalyst cannot take into account it is low Warm, highly selective, high activity, preferable temperature tolerance, cheap and advantage with long service life, and preparation process is multiple It is miscellaneous.
Invention content
The present invention is to solve the catalyst for being currently used for gas phase selective catalytic oxidation alcohol and preparing corresponding aldehydes or ketones cannot The problem of taking into account low temperature, highly selective, high activity, preferable temperature tolerance, longer service life, and low-temperature gaseous phase is provided The method that selective catalytic oxidation benzyl alcohol prepares benzaldehyde.
The molecular formula of catalyst of the present invention is xCu-yZn/CNTS, wherein the x is the matter of Ni metal in the catalyst Percentage composition is measured, x is 0.01%~20%;The y is the mass percentages of metal Zn in the catalyst, y 0.1% ~30%.
The preparation method of the present invention, carries out according to the following steps:
By CNTS carrier impregnations in Cu2+/Zn2It is then 20 DEG C~100 DEG C and speed in temperature in+mixed aqueous solution For magnetic agitation 2h under conditions of 60 turns/min~1000 turn/min~for 24 hours, filtering obtains solid catalyst, then will obtain Solid catalyst to be placed in temperature be dry 1h~48h in 50 DEG C~200 DEG C of baking oven, then be placed at a temperature of 400 DEG C~700 DEG C 1h~for 24 hours is roasted to get to xCu-yZn/CNTS;The wherein x is the mass percentage of Ni metal in the catalyst, x It is 0.01%~20%;The y is the mass percentages of metal Ag in the catalyst, and y is 0.1%~30%;Described Cation is Cu2+ and Zn2+, and Cu2+ in the Cu2+/Zn2+ mixed aqueous solutions in Cu2+/Zn2+ mixed aqueous solutions A concentration of 0.001mol/L~5mol/L, a concentration of 0.001mol/L of Zn2+ in the Cu2+/Zn2+ mixed aqueous solutions~ 5mol/L。
The Cu2+ ion sources are any one of copper nitrate, copper chloride, copper bromide, copper sulphate.Zn2+ ion sources For any one of zinc nitrate, zinc chloride, zinc bromide, zinc sulfate.
Molecular formula is in xCu-yZn/CNTS, and x is preferably 0.1%~10%;Y is preferably 0.1%~5%.
Carbon nanotube also known as Baji-tube mainly constitute several layers to tens of layers coaxial by the carbon atom of hexagonal arrangement Pipe forms, and is found by Japanese Electronic Speculum scholar Iijima.Once it has been observed that having started the research of carbon nanotube in every field The content of upsurge, research includes:Preparation, performance and the application of carbon nanotube.By research it is found that vapour deposition process can be with Synthesizing carbon nanotubes on a large scale so that the cost of carbon nanotube is effectively reduced, this is also that the application of carbon nanotube carries Solid foundation is supplied.The research of carbon nanotube performance is disclosed:Carbon nanotube is a kind of allotrope of carbon, and aperture can With from several nanometers to 100nm.Due to it be by graphite develop come, thus still have a large amount of unpaired electrons along tube wall travelling, In fact, carbon nanotube had not only had the electric conductivity of metal, but also there is semiconducting behavior, is particularly due to certain special defects It may lead to the same carbon pipe not only property with metal, but also the property with semiconductor.By being introduced on Single Carbon Nanotubes Defect, then the position by adjusting defect on the carbon nanotubes can change and adjust this of carbon nanotube in very large range Electrical property.And specific surface area of carbon nanotube is big, hardness is high, has high thermal stability.The particularity of carbon nanotube causes to answer it Extensive research, it is no exception in catalytic science field.In view of many characteristics of carbon nanotube, people carried out as The research of catalyst carrier.
The application of the present invention is will to be used to low-temperature gaseous phase selective catalytic oxidation alcohol prepare in corresponding aldehydes or ketones as catalysis Agent uses.
Catalyst xCu-yZn/CNTS is fitted into atmospheric fixed bed reactor, is squeezed into the alcohol of liquid using charge pump The benzyl alcohol of liquid is set to completely vaporize in 206 DEG C~300 DEG C of preheating furnace, the alcohol after being vaporized, then with the alcohol after vaporization Gas flow be X, take the gas flow of oxygen in oxygen source as Y and with the gas flow of N2 be Z by after vaporization alcohol, oxygen source and N2 is passed into atmospheric fixed bed reactor simultaneously, and successive reaction is to get to phase under conditions of temperature is 210 DEG C~400 DEG C This formaldehyde answered;The ratio of the gas flow X of this methanol after the vaporization and gas flow Y of oxygen in oxygen source is (0.01 ~10):1;The ratio of the gas flow Z of the N2 and gas flow Y of oxygen in oxygen source is (0.01~100):1;Described Catalyst quality and the rate of charge of the quality of the alcohol after vaporization indicate that weight (hourly) space velocity (WHSV) is 0.01h-1~1000h- with weight (hourly) space velocity (WHSV) 1;The oxygenous mixed gas that the oxygen source is oxygen or volume fraction is m, wherein 50%≤m < 100%.
Advantages of the present invention:
1, for catalyst of the invention using method preparation is soaked, synthesis technology is simple;Intermetallic interaction makes activearm Divide and be highly dispersed at carrier surface, and the reduction of content of metal has been obviously shortened production cost;
2, catalyst activity of the invention is high, selectivity is strong, with excellent catalytic performance, and product purity is high, reduction point Cost from purification;And catalyst has good temperature tolerance, and within the scope of very wide temperature (220 DEG C~400 DEG C), tool There is stable catalytic performance, the stable structure in gas phase successive reaction, service life is long and easily-activated regeneration;
3, the Catalyst packing of the present invention is used for low-temperature gaseous phase selective catalytic oxidation in fixed bed continuous reactor Alcohol prepares the reaction of corresponding aldehydes or ketones, can realize the low-temperature gaseous phase high-selectivity oxidation of alcohol under the premise of providing greater activity Corresponding aldehydes or ketones are synthesized, energy consumption is reduced;It is beneficial to the industrialized production for realizing that alcohol gaseous oxidation prepares corresponding aldehydes or ketones, meets green Colour chemistry demand for development;
4, for the present invention using oxygen as oxygen source, by-product is water, free from environmental pollution.
Specific implementation mode
Below in conjunction with the embodiment of the present invention, technical scheme in the embodiment of the invention is clearly and completely described, Obviously, described embodiments are only a part of the embodiments of the present invention, instead of all the embodiments.Based in the present invention The every other implementation that domain those of ordinary skill is obtained without making creative work is added in embodiment, ability Example, shall fall within the protection scope of the present invention.
【Embodiment 1】
By CNTS carrier impregnations in the mixed aqueous solution of copper nitrate and zinc nitrate, Cu2+'s is dense in the mixed aqueous solution Degree is 0.3mol/L, a concentration of 3mol/L of Zn2+.Then magnetic force under conditions of temperature is 50 DEG C and speed is 80 turns/min For 24 hours, filtering obtains solid catalyst for stirring, is then placed in obtained solid catalyst dry in the baking oven that temperature is 100 DEG C For 24 hours, then 700 DEG C of roasting temperature 3h are placed in get to 0.2%Cu-1.8%Zn/CNTS;
Catalyst 0.2%Cu-1.8%Zn/CNTS is fitted into atmospheric fixed bed reactor, using charge pump by liquid Alcohol, which is squeezed into 250 DEG C of preheating furnace, makes the benzyl alcohol of liquid completely vaporize, the benzyl alcohol after being vaporized, benzyl alcohol gas flow Gas flow ratio with oxygen is 1:1 uses internal diameter for 10 millimeters of stainless steel reactor, and loaded catalyst is 10 milliliters, instead It is 220 DEG C to answer temperature, is reacted under normal pressure, and raw material is 80% benzyl alcohol, air speed 6 hours‐1.Reaction product is distinguished after gas-liquid separation Analysis, reaction result are shown in Table 1.
【Embodiment 2】
By CNTS carrier impregnations in the mixed aqueous solution of copper nitrate and zinc nitrate, Cu2+'s is dense in the mixed aqueous solution Degree is 3mol/L, a concentration of 0.2mol/L of Zn2+.Then magnetic under conditions of temperature is 100 DEG C and speed is 200 turns/min Power stirs for 24 hours, and filtering obtains solid catalyst, and then obtained solid catalyst is placed in the baking oven that temperature is 100 DEG C and is done It is dry for 24 hours, then be placed in 700 DEG C of roasting temperature 5h to get to 2.3%Cu-0.3%Zn/CNTS;
Catalyst 2.3%Cu-0.3%Zn/CNTS is fitted into atmospheric fixed bed reactor, using charge pump by liquid Alcohol, which is squeezed into 250 DEG C of preheating furnace, makes the benzyl alcohol of liquid completely vaporize, the benzyl alcohol after being vaporized, benzyl alcohol gas flow Gas flow ratio with oxygen is 1:1 uses internal diameter for 10 millimeters of stainless steel reactor, and loaded catalyst is 10 milliliters, instead It is 240 DEG C to answer temperature, is reacted under normal pressure, and raw material is 80% benzyl alcohol, air speed 12 hours‐1.Reaction product is divided after gas-liquid separation It does not analyze, reaction result is shown in Table 1.
【Embodiment 3】
By CNTS carrier impregnations in the mixed aqueous solution of copper nitrate and zinc nitrate, Cu2+'s is dense in the mixed aqueous solution Degree is 3mol/L, a concentration of 4.2mol/L of Zn2+.Then magnetic under conditions of temperature is 100 DEG C and speed is 200 turns/min Power stirs for 24 hours, and filtering obtains solid catalyst, and then obtained solid catalyst is placed in the baking oven that temperature is 100 DEG C and is done It is dry for 24 hours, then be placed in 600 DEG C of roasting temperature 5h to get to 2.3%Cu-3.8%Zn/CNTS;
Catalyst 2.3%Cu-3.8%Zn/CNTS is fitted into atmospheric fixed bed reactor, using charge pump by liquid Alcohol, which is squeezed into 250 DEG C of preheating furnace, makes the benzyl alcohol of liquid completely vaporize, the benzyl alcohol after being vaporized, benzyl alcohol gas flow Gas flow ratio with oxygen is 1:1 uses internal diameter for 10 millimeters of stainless steel reactor, and loaded catalyst is 10 milliliters, instead It is 260 DEG C to answer temperature, is reacted under normal pressure, and raw material is 80% benzyl alcohol, air speed 10 hours‐1.Reaction product is divided after gas-liquid separation It does not analyze, reaction result is shown in Table 1.
Table 1
Above description has fully disclosed the specific implementation mode of the present invention.It should be pointed out that being familiar with the field Technical staff is to any change for being done of specific implementation mode of the present invention all without departing from the range of claims of the present invention. Correspondingly, the scope of the claims of the invention is also not limited only to previous embodiment.

Claims (10)

1. a kind of method that catalysis oxidation benzyl alcohol prepares benzaldehyde, it is characterised in that:Catalyst xCu-yZn/CNTS is packed into In atmospheric fixed bed reactor, the alcohol of liquid is squeezed into the benzene first for making liquid in 206 DEG C~300 DEG C of preheating furnace using charge pump Alcohol completely vaporizes, the alcohol after being vaporized, and alcohol, oxygen source and the N2 after vaporization are passed into atmospheric fixed bed reactor simultaneously, Successive reaction is to get to this corresponding formaldehyde under conditions of temperature is 210 DEG C~400 DEG C;The catalyst xCu-yZn/ CNTS, wherein the x is the mass percentage of Ni metal in the catalyst, x is 0.01%~20%;The y is gold Belong to the mass percentages of Zn in the catalyst, y is 0.1%~30%.
2. the method that catalysis oxidation benzyl alcohol according to claim 1 prepares benzaldehyde, it is characterised in that:By CNTS carriers It is immersed in Cu2+/Zn2In+mixed aqueous solution, then temperature be 20 DEG C~100 DEG C and speed be 60 turns/min~1000 turn/ Magnetic agitation 2h under conditions of min~for 24 hours, filtering obtains solid catalyst, obtained solid catalyst is then placed in temperature For dry 1h~48h in 50 DEG C~200 DEG C of baking ovens, then be placed in 400 DEG C~700 DEG C roasting temperature 1h~for 24 hours to get to xCu‐yZn/CNTS。
3. the method that catalysis oxidation benzyl alcohol according to claim 2 prepares benzaldehyde, it is characterised in that:The Cu2+ from Sub- source is any one of copper nitrate, copper chloride, copper bromide, copper sulphate.
4. the method that catalysis oxidation benzyl alcohol according to claim 2 prepares benzaldehyde, it is characterised in that:Zn2+ ions come Source is any one of zinc nitrate, zinc chloride, zinc bromide, zinc sulfate.
5. the method that catalysis oxidation benzyl alcohol according to claim 2 prepares benzaldehyde, it is characterised in that:X is preferably 0.1%~10%;Y is preferably 0.1%~5%.
6. the method that catalysis oxidation benzyl alcohol according to claim 2 prepares benzaldehyde, it is characterised in that:The Cu2 In +/Zn2+ mixed aqueous solutions cation be Cu2+ and Zn2+, and in the Cu2+/Zn2+ mixed aqueous solutions Cu2+ concentration For 0.001mol/L~5mol/L, a concentration of 0.001mol/L~5mol/ of Zn2+ in the Cu2+/Zn2+ mixed aqueous solutions L。
7. the method that catalysis oxidation benzyl alcohol according to claim 1 prepares benzaldehyde, it is characterised in that:The vaporization The ratio of the gas flow of oxygen is (0.01~10) in the gas flow and oxygen source of this methanol afterwards:1.
8. the method that catalysis oxidation benzyl alcohol according to claim 1 prepares benzaldehyde, it is characterised in that:The vaporization The ratio of the gas flow of oxygen is (0.01~10) in the gas flow and oxygen source of this methanol afterwards:1.
9. the method that catalysis oxidation benzyl alcohol according to claim 1 prepares benzaldehyde, it is characterised in that:The N2's The ratio of gas flow and the gas flow of oxygen in oxygen source is (0.01~100):1.
10. the method that catalysis oxidation benzyl alcohol according to claim 1 prepares benzaldehyde, it is characterised in that:Described urges Agent quality and the rate of charge of the quality of the alcohol after vaporization indicate that weight (hourly) space velocity (WHSV) is 0.01h-1~1000h-1 with weight (hourly) space velocity (WHSV).
CN201810349635.0A 2018-04-18 2018-04-18 A kind of method that catalysis oxidation benzyl alcohol prepares benzaldehyde Pending CN108640824A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109879741A (en) * 2019-01-30 2019-06-14 东莞理工学院 A kind of green high-efficient method of catalytic oxidation of benzyl alcohol production benzaldehyde
CN111420659A (en) * 2020-04-21 2020-07-17 王永芝 Single noble metal catalyst for gas-solid phase reaction and preparation method thereof

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101456798A (en) * 2008-12-18 2009-06-17 浙江工业大学 Process for synthesizing benzaldehyde
CN101564692A (en) * 2009-06-01 2009-10-28 西北大学 Benzyl alcohol selective oxidation catalyst, preparation method and application thereof
CN103586066A (en) * 2013-11-25 2014-02-19 齐齐哈尔大学 Thermometal modified SBA-15 catalyst, preparation method and application thereof
CN105664926A (en) * 2016-03-09 2016-06-15 广东工业大学 Catalyst for preparing benzaldehyde through selective oxidation of phenylcarbinol and preparing method thereof
CN106831371A (en) * 2016-12-29 2017-06-13 南京工业大学 Novel method for preparing benzaldehyde through catalytic oxidation
CN106975495A (en) * 2017-03-10 2017-07-25 华东师范大学 A kind of preparation and its application of carborundum supported copper bimetallic catalyst
CN107141211A (en) * 2017-07-03 2017-09-08 广西大学 A kind of preparation method of benzaldehyde
CN107597109A (en) * 2017-08-09 2018-01-19 华东师范大学 Load type gold catalyst of nano-metal-oxide doping and preparation method and application

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101456798A (en) * 2008-12-18 2009-06-17 浙江工业大学 Process for synthesizing benzaldehyde
CN101564692A (en) * 2009-06-01 2009-10-28 西北大学 Benzyl alcohol selective oxidation catalyst, preparation method and application thereof
CN103586066A (en) * 2013-11-25 2014-02-19 齐齐哈尔大学 Thermometal modified SBA-15 catalyst, preparation method and application thereof
CN105664926A (en) * 2016-03-09 2016-06-15 广东工业大学 Catalyst for preparing benzaldehyde through selective oxidation of phenylcarbinol and preparing method thereof
CN106831371A (en) * 2016-12-29 2017-06-13 南京工业大学 Novel method for preparing benzaldehyde through catalytic oxidation
CN106975495A (en) * 2017-03-10 2017-07-25 华东师范大学 A kind of preparation and its application of carborundum supported copper bimetallic catalyst
CN107141211A (en) * 2017-07-03 2017-09-08 广西大学 A kind of preparation method of benzaldehyde
CN107597109A (en) * 2017-08-09 2018-01-19 华东师范大学 Load type gold catalyst of nano-metal-oxide doping and preparation method and application

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
I.ESWARAMOORTHI ET AL.等: "Partial oxidation of methanol for hydrogen production over carbon nanotubes supported Cu-Zn catalysts", 《APPLIED CATALYSIS A: GENERAL》 *
MEHDI FOROUZANI ET AL.等: "Comparative study of oxidation of benzyl alcohol: Influence of Cu-doped metal cation on nano ZnO catalytic activity", 《CHEMICAL ENGINEERING JOURNAL》 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109879741A (en) * 2019-01-30 2019-06-14 东莞理工学院 A kind of green high-efficient method of catalytic oxidation of benzyl alcohol production benzaldehyde
CN109879741B (en) * 2019-01-30 2023-01-13 东莞理工学院 Green and efficient method for producing benzaldehyde by catalytic oxidation of benzyl alcohol
CN111420659A (en) * 2020-04-21 2020-07-17 王永芝 Single noble metal catalyst for gas-solid phase reaction and preparation method thereof
CN111420659B (en) * 2020-04-21 2022-08-09 湖北荟煌科技股份有限公司 Noble metal catalyst

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