CN108014794B - Synthesize hydrogenation catalyst used in 1,4- diacetoxy butane - Google Patents
Synthesize hydrogenation catalyst used in 1,4- diacetoxy butane Download PDFInfo
- Publication number
- CN108014794B CN108014794B CN201610967708.3A CN201610967708A CN108014794B CN 108014794 B CN108014794 B CN 108014794B CN 201610967708 A CN201610967708 A CN 201610967708A CN 108014794 B CN108014794 B CN 108014794B
- Authority
- CN
- China
- Prior art keywords
- catalyst
- isosorbide
- nitrae
- diacetoxy butane
- diacetoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/63—Platinum group metals with rare earths or actinides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/62—Platinum group metals with gallium, indium, thallium, germanium, tin or lead
- B01J23/622—Platinum group metals with gallium, indium, thallium, germanium, tin or lead with germanium, tin or lead
- B01J23/626—Platinum group metals with gallium, indium, thallium, germanium, tin or lead with germanium, tin or lead with tin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/62—Platinum group metals with gallium, indium, thallium, germanium, tin or lead
- B01J23/622—Platinum group metals with gallium, indium, thallium, germanium, tin or lead with germanium, tin or lead
- B01J23/628—Platinum group metals with gallium, indium, thallium, germanium, tin or lead with germanium, tin or lead with lead
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/28—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
- C07C67/283—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by hydrogenation of unsaturated carbon-to-carbon bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
The present invention relates to synthesis 1, hydrogenation catalyst used in 4- diacetoxy butane, mainly solve in the prior art 1, the low problem of the yield and selectivity of 4- diacetoxy butane, using synthesis 1, hydrogenation catalyst used in 4- diacetoxy butane, including carrier and active component, the carrier is active carbon, active component includes Pt element and promoter elements, the promoter elements include the technical solution selected from least one of lanthanide series metal at least one of metallic element and IVA race metal metallic element, preferably solves the technical problem, it can be used for 1, in the industrial production of 4- diacetoxy butane.
Description
Technical field
The present invention relates to hydrogenation catalysts used in synthesis 1,4- diacetoxy butane.
Background technique
1,4-butanediol (Isosorbide-5-Nitrae-BDO) is a kind of important organic and fine chemical material, it be widely used in medicine,
The fields such as chemical industry, weaving, papermaking, automobile and daily-use chemical industry.It can derive a series of fine chemical product of high added values.
For example, tetrahydrofuran (THF), polybutylene terephthalate (PBT) (PBT), γ-fourth lactones (GBL) can be produced by Isosorbide-5-Nitrae-BDO
It is ground with polyurethane resin (PU Resin) especially as the base stock of production PBT engineering plastics and PBT fiber
Study carefully the extensive concern of mechanism.
The process route of the preparation of 1,4-butanediol is relatively more, and dividing from raw material used has acetylene, ethylene, propylene, fourth
The raw material routes such as diene and cis-butenedioic anhydride, identical raw material also have different synthesis technologies.Since technical barrier is higher and raw material sources
Limited, global Isosorbide-5-Nitrae-BDO produces Relatively centralized.2011, global Isosorbide-5-Nitrae-BDO production capacity was mainly distributed on Asia, US and European,
Wherein Asia 1,4-BDO production capacity accounting is up to 56.6%.Currently, the industrialized preparing process of Isosorbide-5-Nitrae-BDO specifically includes that 1. alkynes aldehyde
Method (Reppe method): this method makees catalyst using methanol copper and generates butynediols, butynediols using acetylene and formaldehyde as raw material
Two-stage hydrogenation obtains 1,4-BDO again.Its prevailing technology mainly have BASF Corp. of Germany, the U.S. DuPont exploitation Reppe method with
And the Reppe method of improvement.2. maleic anhydride process: this method carries out two steps to it and adds hydrogen using cis-butenedioic anhydride as raw material.The first step is urged in Ni-Re
Under agent effect, maleic anhydride hydrogenation generates gamma-butyrolacton and tetrahydrofuran;Second step gamma-butyrolacton is in Mo-Cr-K2O catalyst is made
1,4-BDO is hydrogenated under.Its prevailing technology is mainly with the two-stage hydrogenation work of Japanese two water chestnut oilings and Mitsubishi's chemical conversion exploitation
Skill.3. propylene method: mainly including allyl acetate method, acryladehyde method and allyl acetate-allyl alcohol method, Kuraray company develops at present
Allyl acetate-allyl alcohol method has obtained industrial application, it is under rhodium catalyst, and allyl alcohol liquid-phase hydrogenatin formylated generates 4- hydroxyl fourth
Aldehyde, then repeated hydrogenation generates 1,4-butanediol.4. butadiene process: the method that Isosorbide-5-Nitrae-BDO is produced as raw material using butadiene, it is main to wrap
Butadiene acetoxylation method and butadiene chloridising are included, the technique of mainstream is by Mitsubishi chemical conversion and Cao Da company in 20 generation
It records 80 years and develops, it successfully breaks the technical barrier and obstacle of Reppe method.Especially butadiene acetoxylation method is excellent
Gesture and prospect have obtained the favor of domestic and international research institution.
It is well known that butadiene acetoxylation method is a three-steps process, i.e., butadiene and acetic acid, oxygen first is sent out
Raw acetylization reaction, generates Isosorbide-5-Nitrae-diacetoxy butylene and by-product 3.4- diacetoxy butylene;Then 1,4- diacetyl
Oxygroup butylene catalytic hydrogenation generates Isosorbide-5-Nitrae-diene acetoxyl group butane, and reaction is finally hydrolyzed and obtains Isosorbide-5-Nitrae-BDO.In Isosorbide-5-Nitrae-fourth
For diene into 1,4-butanediol process route, Isosorbide-5-Nitrae-diacetoxy butylene catalytic hydrogenation generates Isosorbide-5-Nitrae-diene acetoxyl group butane
As one of step, the yield and selectivity of hydrogenation products directly influence 1,4-butanediol relative to Isosorbide-5-Nitrae-butadiene
Yield and selectivity.
It teaches in the patents such as patent US4032458 (production of 1,4-butanediol) and is being urged using furans
Agent exists, and prepares 1,4-butanediol under the conditions of certain temperature and pressure.Patent CN94108094.3 (the system of 1,4- butanediol
Preparation Method) it describes using cis-butenedioic anhydride as raw material, gas phase catalytic hydrogenation reaction preparation is carried out in the presence of the catalyst specifically designed
1,4- butanediol.Patent CN104326871A (a kind of preparation method of butanediol) is described using fixed-bed catalytic technology, will
Content greater than 99% 2- butylene mixed with acetic acid, nitrogen, oxygen and water vapour high temperature after be passed through in fixed bed, catalyst with
1,4- butanediol is prepared under the conditions of certain temperature, pressure etc..But there is 1,4- during preparing 1,4-BDO in the above method
The problem that BDO yield is low and selectivity is not high.
Summary of the invention
The technical problem to be solved by the present invention is to the low problems of the yield of 1,4-butanediol and selectivity, provide a kind of new
Synthesis Isosorbide-5-Nitrae-diacetoxy butane used in hydrogenation catalyst, the catalyst have Isosorbide-5-Nitrae-diacetoxy butane high income
The high feature with selectivity.
The second technical problem to be solved by the present invention is the preparation method of above-mentioned hydrogenation catalyst.
The third technical problem to be solved by the present invention is the 1,4- diacetoxy butane using above-mentioned hydrogenation catalyst
Synthetic method.
One of in order to solve the above-mentioned technical problem, The technical solution adopted by the invention is as follows: synthesis Isosorbide-5-Nitrae-diacetoxy
Hydrogenation catalyst used in butane, including carrier and active component, the carrier are active carbon, and active component includes Pt element
And promoter elements, the promoter elements include selected from least one of lanthanide series metal metallic element and IVA race metal
At least one of metallic element.
In above-mentioned technical proposal, the active carbon is preferably coal quality column charcoal, cocoanut active charcoal, apricot shell active carbon and bamboo matter
At least one of active carbon.
In above-mentioned technical proposal, the specific surface area of the active carbon is preferably 1000~1500cm2/ g, adsorption hole hold preferred
For 0.60~1.00cm3/g。
In above-mentioned technical proposal, in the hydrogenation catalyst group of the lanthanides race metal preferably be selected from La, Ce, Pr, Nd, Sm, Eu, Yb and
At least one of Lu.It further simultaneously include La, Lu.La, Lu are improving 1,4- diethyl acyl-oxygen butane yield and 1,4- bis-
Acetyl oxygen butane selectivity aspect has synergistic effect.
In above-mentioned technical proposal, IVA race metal is selected from least one of Ge, Sn and Pb in the hydrogenation catalyst, more
It further preferably simultaneously include Sn and Pb.Sn and Pb is improving 1,4- diethyl acyl-oxygen butane yield and the choosing of 1,4- diethyl acyl-oxygen butane
There is synergistic effect in terms of selecting property.
In above-mentioned technical proposal, the promoter elements preferably include at least one in lanthanide element simultaneously
Kind and at least one of selected from IVA race metallic element, at this time in the metallic element in group of the lanthanides and IVA race metal metallic element it
Between there is synergistic effect in terms of improving 1,4- diethyl acyl-oxygen butane yield and 1,4- diethyl acyl-oxygen butane selectivity.As non-limit
Property citing processed, such as, but not limited to lanthanum is cooperateed with tin, and lanthanum is cooperateed with lead etc..
In above-mentioned technical proposal, the content of Pt is preferably 1.00~8.00g/L in the hydrogenation catalyst, more preferably
1.50~5.00g/L.
In above-mentioned technical proposal, promoter elements content is preferably 0.50~10.00g/L in the hydrogenation catalyst,
More preferably 1.00~6.00g/L.
To solve above-mentioned technical problem two, technical scheme is as follows:
Hydrogenation catalyst preparation method described in any one of technical solution of one of above-mentioned technical problem, including walk as follows
It is rapid:
1. mixing the solution of platiniferous element with carrier by the composition of catalyst, catalyst precarsor I is obtained;
2. obtaining catalyst precarsor II after catalyst precarsor I is aged;
3. being simple substance platinum by compound state platinum element reduction in catalyst precarsor II, catalyst precarsor III is obtained;
4. being washed, being dried to obtain catalyst precarsor IV;
5. the solution containing promoter elements is supported on catalyst precarsor IV using infusion process by the composition of catalyst,
It is dried to obtain the catalyst.
In above-mentioned technical proposal, as non-restrictive, 1. the corresponding particular compound of platinum element preferably is selected from vinegar to step
At least one of sour platinum, platinum chloride, ammonium chloroplatinite, dinitroso diammonia platinum, chloroplatinic acid and four ammino platinum chlorides;More preferably
Ammonium chloroplatinite.
In above-mentioned technical proposal, as non limiting example, when step 5. in promoter elements include lanthanide series metal
When element, the corresponding particular compound of lanthanide element preferably be selected from lanthanum acetate, lanthanum nitrate, lanthanum chloride, lanthanum sulfate, cerium chloride,
Cerous nitrate, cerous acetate, praseodymium acetate, praseodymium chloride, praseodymium nitrate, acetic acid neodymium, neodymium chloride, acetic acid samarium, samarium trichloride, samaric nitrate, Europium chloride,
At least one of europium nitrate, acetic acid europium, acetic acid ytterbium, ytterbium chloride, ytterbium nitrate, lutecium chloride, lutecium nitrate and acetic acid lutetium;More preferably certainly
At least one of lanthanum acetate and acetic acid lutetium.
In above-mentioned technical proposal, as non limiting example, when step 5. in promoter elements include IVA race metal
When element, it is sub- that the corresponding particular compound of IVA race metallic element preferably is selected from tetraethyl germanium, tetraphenyl germanium, germanium tetrachloride, oxalic acid
Tin, stannous chloride, nitric acid stannous, stannous acetate, stannous oxide, lead acetate, lead stearate, basic lead carbonate, basic lead acetate
At least one of with plumbi nitras;More preferably from least one of stannous acetate and lead acetate.
In above-mentioned technical proposal, the reducing agent of step 3. does not specially require understanding based on those skilled in the art, also
Former agent can be at least one of gas or liquid, the preferred hydrogen of reducing agent, hydrazine hydrate;4. drying temperature is preferably step
30~120 DEG C, drying time is preferably 1~5 hour;5. the drying temperature is preferably 80~120 DEG C to step, more preferably
100~120 DEG C.
To solve above-mentioned technical problem three, technical scheme is as follows:
Isosorbide-5-Nitrae-diacetoxy butane synthetic method, described in any one of technical solution of one of above-mentioned technical problem
In the presence of hydrogenation catalyst, hydrogen and Isosorbide-5-Nitrae-diacetoxy butene reaction obtain Isosorbide-5-Nitrae-diacetoxy butane.
Key of the invention is the selection of hydrogenation catalyst, and skilled person will know how determine according to actual needs
Suitable hydrogenation process conditions reaction temperature, reaction time, reaction pressure and proportion of material etc..But:
In above-mentioned technical proposal, the temperature of hydrogenation reaction is preferably 20~120 DEG C.
In above-mentioned technical proposal, the pressure of hydrogenation reaction is preferably 1.0~10.0MPa, more preferable 1.0~6.0MPa.
In above-mentioned technical proposal, the time of hydrogenation reaction is preferably 0.5~5.0h, more preferable 0.5~2.0h.
Isosorbide-5-Nitrae-diacetoxy butylene can be obtained from commercially available channel, or the synthesis of butadiene Acetoxylation method can be used.Fourth
It is butadiene Acetoxylation catalyst that diene Acetoxylation method, which synthesizes and Pd-Te/C can be selected,.Palladium in suitable Pd-Te/C catalyst
The content of element preferably 2.50~5.00g/L, more preferable 3.00~4.50g/L;The content of tellurium element preferably 0.50~3.00g/
L, more preferable 1.00~2.50g/L.Suitable Acetoxylation reaction temperature is preferably 40~150 DEG C;Acetoxylation reaction pressure
It is preferred that 1.0~10.0MPa;The Acetoxylation reaction time is preferably 0.5~5h;The molar ratio of butadiene and acetic acid preferably 0.010
~2.0.After the reaction of butadiene Acetoxylation, the mixture that can be reacted butadiene Acetoxylation carries out separation and obtains target production
Object Isosorbide-5-Nitrae-diacetoxy butylene carries out hydrogenation reaction of the present invention again, can not also separate and directly carry out hydrogenation reaction.But
Cause system complexity convenient on year-on-year basis, specific embodiment of the invention department is all made of pure Isosorbide-5-Nitrae-diacetyl to exclude other impurity
Oxygroup butylene is as hydrogenation reaction raw material.
The product mixtures of above-mentioned hydrogenation reaction can obtain target product 1,4- diacetoxy butane through separation.
1,4- diacetoxy butane can be further used for obtaining 1,4- butanediol by method for hydrolysis.Art technology
The suitable hydrolyst of the known selection of personnel and determining suitable hydrolysising reacting temperature, time and material proportion.Common water
Solution catalyst can be inorganic acid, inorganic base, organic acid and organic base.Such as hydrochloric acid, nitric acid, sulfuric acid, phosphoric acid, sodium hydroxide,
Potassium hydroxide, benzene sulfonic acid and ion exchange resin.Suitable hydrolysising reacting temperature is preferably 30~100 DEG C;Hydrolysis pressure
Power preferably 0~2.0MPa;The preferred water of solvent.
Product mixtures after hydrogenation reaction of the present invention are analyzed through gas chromatograph-mass spectrometer (GC-MS) (GC-MASS), by following
The yield and selectivity of formula calculating 1,4- diacetoxy butane:
Compared with prior art, hydrogenation catalyst of the present invention improves Isosorbide-5-Nitrae-diethyl acyl-oxygen butane yield and selectivity.
The experimental results showed that Isosorbide-5-Nitrae-diacetoxy butane yield selectively reaches up to 82.49% when using the present invention
94.18%, achieve preferable technical effect.It simultaneously include especially platinum, selected from group of the lanthanides in the active component of hydrogenation catalyst
At least one of metal metallic element and when selected from least one of IVA race metal metallic element, achieves more prominent
Technical effect.Below by embodiment, the present invention is further elaborated.
Specific embodiment
[embodiment 1]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the lanthanum acetate (La (OAc) of the La containing 1.90g3·5H2O aqueous solution 180ml) is immersed in catalyst precarsor IV
On, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, La content 1.90g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 82.49% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 94.18%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[embodiment 2]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the lead acetate (Pb (OAc) of the Pb containing 1.90g2·3H2O) aqueous solution 180ml is immersed on catalyst precarsor IV,
110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, Pb content 1.90g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 82.35% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 94.24%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[comparative example 1]
For the comparative example of [embodiment 1] and [embodiment 2].
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 75.15% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 91.33%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
By the way that, as can be seen that the present invention is using the catalyst for adding hydrogen, active component makes simultaneously compared with Examples 1 to 2
With containing Pt, La active component, simultaneously the catalyst performance containing Pt, Pb active component than the performance containing only Pt active constituent catalyst
It is more excellent, illustrate activity of hydrocatalyst component and meanwhile include using containing Pt and in lanthanide series metal and IVA race metal extremely
A kind of few metallic element compound is conducive to the activity and stability that improve hydrogenation catalyst, Isosorbide-5-Nitrae-diacetoxy butane
Yield and selectivity will be high.
[comparative example 2]
For the comparative example of [comparative example 1].
The preparation of hydrogenation catalyst:
1. by the ammonium chloropalladite ((NH containing 2.05gPd4)2PdCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain the catalyst.
The Pd content for measuring the catalyst through ICP is 2.05g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 70.10% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 88.03%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
By can be seen that the present invention compared with comparative example 1 using the catalyst for adding hydrogen, contained using the ratio of active component containing Pt
The performance of Pd active constituent catalyst is more excellent, illustrates that activity of hydrocatalyst component is conducive to Isosorbide-5-Nitrae-diacetoxy using Pt
Butylene adds hydrogen, and Isosorbide-5-Nitrae-diacetoxy butane yield and selectivity will be high.
[embodiment 3]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the stannous acetate (Sn (OAc) of the Sn containing 1.90g2·2H2O) it is dissolved in the aqueous acetic acid that concentration is 10wt%
In, obtain maceration extract 180ml, be immersed on catalyst precarsor IV, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, Sn content 1.90g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 82.38% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 94.29%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[embodiment 4]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.60cm3/ g, specific surface area 1000cm2The coconut husk circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the cerous acetate (Ce (OAc) of the Ce containing 1.90g3·6H2O) aqueous solution 180ml is immersed on catalyst precarsor IV,
100 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, Ce content 1.90g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 82.46% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 94.14%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[embodiment 5]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 1.00cm3/ g, specific surface area 1500cm2The apricot shell circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the praseodymium acetate (Pr (OAc) of the Pr containing 1.90g3·5H2O) aqueous solution 180ml is immersed on catalyst precarsor IV,
120 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, Pr content 1.90g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 82.45% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 94.17%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[embodiment 6]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The bamboo circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the acetic acid neodymium (Nd (OAc) of the Nd containing 1.90g2·6H2O) aqueous solution 180ml is immersed on catalyst precarsor IV,
110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, Nd content 1.90g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 82.47% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 94.14%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[embodiment 7]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the acetic acid lutetium (Lu (OAc) of the Lu containing 1.90g3·6H2O) aqueous solution 180ml is immersed in catalyst precarsor IV
On, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, Lu content 1.90g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 50 DEG C, after sustained response 90min, stops anti-
It answers.
It is 82.45% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 94.20%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[embodiment 8]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 1.50gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the acetic acid europium (Eu (OAc) of the Eu containing 1.00g3·6H2O) aqueous solution 180ml is immersed in catalyst precarsor IV
On, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 1.50g/L, Eu content 1.00g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 1.0MPa, improves mixing speed first with 0.5MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 20 DEG C, after sustained response 30min, stops anti-
It answers.Reaction kettle is down to room temperature, purified removal of impurities obtains Isosorbide-5-Nitrae-diacetoxy butane.
It is 80.62% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 93.92%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[embodiment 9]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 5.00gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the acetic acid ytterbium (Yb (OAc) of the Yb containing 6.00g3·6H2O) aqueous solution 180ml is immersed in catalyst precarsor IV
On, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 5.00g/L, Yb content 6.00g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 6.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 120 DEG C, after sustained response 120min, stops
Reaction.
It is 82.54% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 93.89%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[embodiment 10]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the lanthanum acetate (La (OAc) of La containing the 1.20g and Lu containing 0.70g3·5H2) and acetic acid lutetium (Lu (OAc) O3·
6H2O aqueous solution 180ml) is immersed on catalyst precarsor IV, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, La content 1.20g/L, Lu content 0.70g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 83.43% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 94.35%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
Found out on year-on-year basis by embodiment 10 and embodiment 1 and embodiment 7, is improving Isosorbide-5-Nitrae-diacetoxy butane yield
In the hydrogenation catalyst used with selective aspect, the present invention, metallic element La and metallic element Lu have preferably in lanthanide series metal
Synergistic effect.
[embodiment 11]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the lead acetate (Pb (OAc) of Pb containing the 0.90g and Sn containing 1.00g2·3H2) and stannous acetate (Sn O
(OAc)2·2H2O it) is dissolved in the aqueous acetic acid that concentration is 10wt%, obtains maceration extract 180ml, be immersed in catalyst precarsor
On IV, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, Pb content 0.90g/L, Sn content 1.00g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 83.31% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 94.46%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
Found out on year-on-year basis by embodiment 11 and embodiment 2 and embodiment 3, is improving Isosorbide-5-Nitrae-diacetoxy butane yield
In the hydrogenation catalyst used with selective aspect, the present invention, metallic element Pb and metallic element Sn have preferably in IVA race metal
Synergistic effect.
[embodiment 12]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the lanthanum acetate (La (OAc) of La containing the 1.09g and Pb containing 0.81g3·5H2) and lead acetate (Pb (OAc) O2·
3H2O 180ml in aqueous solution) is immersed on catalyst precarsor IV, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, La content 1.09g/L, Pb content 0.81g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 84.39% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 95.03%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
Found out on year-on-year basis by embodiment 12 and embodiment 1 and embodiment 2, is improving Isosorbide-5-Nitrae-diacetoxy butane yield
In the hydrogenation catalyst used with selective aspect, the present invention, metallic element La and metal member in IVA race metal in lanthanide series metal
Plain Pb has preferable synergistic effect.
[embodiment 13]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the lanthanum acetate (La (OAc) of La containing the 1.09g and Sn containing 0.81g3·5H2) and stannous acetate (Sn O
(OAc)2·2H2O it) is dissolved in the aqueous acetic acid that concentration is 10wt%, obtains maceration extract 180ml, be immersed in catalyst precarsor
On IV, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, La content 1.09g/L, Sn content 0.81g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 84.33% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 95.11%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
Found out on year-on-year basis by embodiment 13 and embodiment 1 and embodiment 3, is improving Isosorbide-5-Nitrae-diacetoxy butane yield
In the hydrogenation catalyst used with selective aspect, the present invention, metallic element La and metal member in IVA race metal in lanthanide series metal
Plain Sn has preferable synergistic effect.
[embodiment 14]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the lanthanum acetate (La (OAc) of La containing 1.09g, Pb containing 0.35g and the Sn containing 0.46g3·5H2O), lead acetate
(Pb(OAc)2·3H2) and stannous acetate (Sn (OAc) O2·2H2O) it is completely dissolved in the aqueous acetic acid that concentration is 10wt%
In, obtain maceration extract 180ml, be immersed on catalyst precarsor IV, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, La content 1.09g/L, Pb content 0.35g/L, Sn content
0.46g/L。
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 85.27% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 95.44%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
Found out on year-on-year basis by embodiment 14 and embodiment 12 and embodiment 13, is improving Isosorbide-5-Nitrae-diacetoxy butane receipts
In terms of rate and selectivity, in the hydrogenation catalyst that the present invention uses, metal in metallic element La and IVA race metal in lanthanide series metal
Elements Pb, Sn have preferable synergistic effect.
[embodiment 15]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the acetic acid lutetium (Lu (OAc) of Lu containing 1.09g, Pb containing 0.35g and the Sn containing 0.46g3·6H2O), lead acetate
(Pb(OAc)2·3H2) and stannous acetate (Sn (OAc) O2·2H2O) it is completely dissolved in the aqueous acetic acid that concentration is 10wt%
In, obtain maceration extract 180ml, be immersed on catalyst precarsor IV, 110 DEG C drying 4 hours, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, Lu content 1.09g/L, Pb content 0.35g/L, Sn content
0.46g/L。
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 85.17% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 95.48%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
[embodiment 16]
The preparation of hydrogenation catalyst:
1. by the ammonium chloroplatinite ((NH containing 2.05gPt4)2PtCl4) be dissolved in the aqueous hydrochloric acid solution that concentration is 8wt%,
Maceration extract 200ml is obtained, by 1L diameter 3mm, long 2cm, Kong Rongwei 0.80cm3/ g, specific surface area 1200cm2The coal quality circle of/g
Column-shaped active carbon carrier impregnation obtains catalyst precarsor I in above-mentioned maceration extract;
2. it is still aging for 24 hours, obtain catalyst precarsor II;
3. being 8% (with N with concentration2H4·H2O weight ratio meter) 500ml hydrazine hydrate catalyst precarsor II is restored
3h obtains catalyst precarsor III;
4. be washed to no chloride ion, 50 DEG C drying 4 hours, obtain catalyst precarsor IV;
5. by the lanthanum acetate (La (OAc) of La containing 0.69g, Lu containing 0.40g, Pb containing 0.35g and the Sn containing 0.46g3·
5H2O), acetic acid lutetium (Lu (OAc)3·6H2O), lead acetate (Pb (OAc)2·3H2) and stannous acetate (Sn (OAc) O2·2H2O it) fills
Divide and be dissolved in the aqueous acetic acid that concentration is 10wt%, obtains maceration extract 180ml, be immersed on catalyst precarsor IV, 110 DEG C
It is 4 hours dry, obtain the catalyst.
The Pt content for measuring the catalyst through ICP is 2.05g/L, La content 0.69g/L, Lu content 0.40g/L, Pb content
0.35g/L, Sn content 0.46g/L.
1,4- diacetoxy butylene hydrogenation reaction:
The reaction of 100ml titanium is added in 1,4- diacetoxy butylene 15ml, toluene 30ml, 0.01mol hydrogenation catalyst
Kettle then passes to hydrogen until pressure 3.0MPa, improves mixing speed first with 1.0MPa is pressurized to after air in argon gas discharge kettle
To 600rpm, while agitating and heating is warming up to reaction temperature, and control reaction temperature is 60 DEG C, after sustained response 90min, stops anti-
It answers.
It is 86.37% through analytical calculation Isosorbide-5-Nitrae-diacetoxy butane yield, selectivity is 95.59%, for the ease of
Illustrate and compare, by the preparation of hydrogenation catalyst, reaction condition, material inlet amount, Isosorbide-5-Nitrae-diacetoxy butane yield and
Selectivity is listed in Tables 1 and 2 respectively.
Found out on year-on-year basis by embodiment 16 and embodiment 14 and embodiment 15, is improving Isosorbide-5-Nitrae-diacetoxy butane receipts
In terms of rate and selectivity, in the hydrogenation catalyst that the present invention uses, in lanthanide series metal in metallic element La, Lu and IVA race metal
Metallic element Pb, Sn have preferable synergistic effect.
Table 1
Table 2
Claims (8)
1. a kind of Isosorbide-5-Nitrae-diacetoxy butane synthetic method, in the presence of a hydrogenation catalyst, hydrogen and Isosorbide-5-Nitrae-diethyl acyl-oxygen
Base butene reaction obtains 1,4- diacetoxy butane;The hydrogenation catalyst, including carrier and active component, the carrier
For active carbon, active component includes Pt element and promoter elements, and the promoter elements include in lanthanide series metal
At least one of at least one metallic element and IVA race metal metallic element.
2. Isosorbide-5-Nitrae according to claim 1-diacetoxy butane synthetic method, which is characterized in that the active carbon is
At least one of coal quality column charcoal, cocoanut active charcoal, apricot shell active carbon and activated carbon from bamboo.
3. Isosorbide-5-Nitrae according to claim 1-diacetoxy butane synthetic method, which is characterized in that the active carbon
Specific surface area is 1000~1500m2/ g, it is 0.60~1.00cm that adsorption hole, which holds,3/g。
4. Isosorbide-5-Nitrae according to claim 1-diacetoxy butane synthetic method, which is characterized in that the hydrogenation catalyst
Lanthanide series metal is selected from least one of La, Ce, Pr, Nd, Sm, Eu, Yb and Lu in agent.
5. Isosorbide-5-Nitrae according to claim 1-diacetoxy butane synthetic method, which is characterized in that the hydrogenation catalyst
Ji Zhong IVA race's metal is selected from least one of Ge, Sn and Pb.
6. Isosorbide-5-Nitrae according to claim 1-diacetoxy butane synthetic method, which is characterized in that the hydrogenation catalyst
Pt constituent content is 1.00~8.00g/L in agent.
7. Isosorbide-5-Nitrae according to claim 1-diacetoxy butane synthetic method, which is characterized in that in hydrogenation catalyst
Promoter elements content is 0.50~10.00g/L.
8. Isosorbide-5-Nitrae according to claim 1-diacetoxy butane synthetic method, which is characterized in that the hydrogenation catalyst
Agent is prepared by the following method, and this method comprises the following steps:
1. mixing the solution of platiniferous element with carrier by the composition of catalyst, catalyst precarsor I is obtained;
2. obtaining catalyst precarsor II after catalyst precarsor I is aged;
3. being simple substance platinum by compound state platinum element reduction in catalyst precarsor II, catalyst precarsor III is obtained;
4. being washed, being dried to obtain catalyst precarsor IV;
5. the solution containing promoter elements is supported on catalyst precarsor IV using infusion process by the composition of catalyst, it is dry
Obtain the catalyst.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610967708.3A CN108014794B (en) | 2016-11-01 | 2016-11-01 | Synthesize hydrogenation catalyst used in 1,4- diacetoxy butane |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610967708.3A CN108014794B (en) | 2016-11-01 | 2016-11-01 | Synthesize hydrogenation catalyst used in 1,4- diacetoxy butane |
Publications (2)
Publication Number | Publication Date |
---|---|
CN108014794A CN108014794A (en) | 2018-05-11 |
CN108014794B true CN108014794B (en) | 2019-10-11 |
Family
ID=62084451
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610967708.3A Active CN108014794B (en) | 2016-11-01 | 2016-11-01 | Synthesize hydrogenation catalyst used in 1,4- diacetoxy butane |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN108014794B (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104368364A (en) * | 2014-11-10 | 2015-02-25 | 华玉叶 | Preparation method of catalyst for preparing propylene by virtue of propane dehydrogenation |
CN105148935B (en) * | 2015-07-18 | 2018-05-08 | 西安凯立新材料股份有限公司 | Produce 2,3,4- trifluoromethyl aniline catalyst and its preparation method and application |
CN104971740B (en) * | 2015-07-18 | 2017-09-12 | 西安凯立新材料股份有限公司 | The continuous catalyst and preparation method and application for preparing the fluoroaniline of N isopropyls 4 |
-
2016
- 2016-11-01 CN CN201610967708.3A patent/CN108014794B/en active Active
Also Published As
Publication number | Publication date |
---|---|
CN108014794A (en) | 2018-05-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN108002978B (en) | The method that butadiene prepares 1,4- butanediol | |
CN107778135B (en) | The method for producing 1,4- butanediol | |
CN108017509B (en) | The method of butadiene production 1,4- butanediol | |
CN108014794B (en) | Synthesize hydrogenation catalyst used in 1,4- diacetoxy butane | |
CN108002979B (en) | The method that butadiene Acetoxylation prepares 1,4- butanediol | |
CN107867972B (en) | The production method of 1,4-butanediol | |
CN107790182B (en) | 1,4- diacetoxy butylene hydrogenation process catalyst | |
CN107774255B (en) | 1,4- diacetoxy butylene hydroprocessing catalysts | |
CN107774336B (en) | Catalyst for 1,4- diacetoxy butylene hydrogenation process | |
CN107774250B (en) | Catalyst for 1,4- diacetoxy butylene hydrogenation technique | |
CN107866217B (en) | Catalyst suitable for the preparation of 1,4- diacetoxy butane | |
CN107778134B (en) | The synthetic method of 1,4- butanediol | |
CN108014793A (en) | Prepare the hydrogenation catalyst used in 1,4- diacetoxy butane | |
CN107999067A (en) | Produce the hydrogenation catalyst used in 1,4- diacetoxy butane | |
CN107774253B (en) | For synthesizing the hydrogenation catalyst of 1,4- diacetoxy butane | |
CN107999064B (en) | The catalyst of butadiene synthesis 1,4- diacetoxy butane course | |
CN107778144B (en) | The method for synthesizing 1,4- butanediol | |
CN107867971B (en) | The preparation method of 1,4-butanediol | |
CN107999066A (en) | Butadiene prepares the catalyst of 1,4- diacetoxy butane processes | |
CN107999065A (en) | Butadiene synthesizes the catalyst of 1,4- diacetoxy butane processes | |
CN107999063A (en) | The catalyst of butadiene production 1,4- diacetoxy butane processes | |
CN107774256A (en) | 1,4 diacetoxy butylene hydrogenation catalysts | |
CN107866233A (en) | Catalyst suitable for the synthesis of 1,4 diacetoxy butane | |
CN107866232A (en) | Catalyst suitable for the production of 1,4 diacetoxy butane | |
CN107774249A (en) | Produce the hydrogenation catalyst of 1,4 diacetoxy butane |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |