SELECTIVE HYDROGENATION CATALYST, PREPARATION METHOD AND APPLICATION THEREOF

Abstract

The present invention discloses a selective hydrogenation catalyst and a preparation method and an application thereof, belonging to the technical field of catalysts. The selective hydrogenation catalyst comprises an active component and a carrier for supporting the active component, wherein the active component is a transition metal particle, the carrier is modified by a flexible chain ligand in advance, one end of the flexible chain ligand is uniformly distributed on the surface of the carrier, and the other end of the flexible chain ligand is coordinated on a transition metal. When the catalyst is used for catalytic hydrogenation reaction of dehydrolinalool or 2-methyl-3-butyn-2-ol, the stability is good, the catalyst still has high selectivity after being used for a long time, and the quality of a hydrogenation product can be guaranteed.

Claims

1. A selective hydrogenation catalyst, comprising an active component and a carrier for supporting the active component, characterized in that the active component is a transition metal particle, the carrier is modified by a flexible chain ligand in advance, one end of the flexible chain ligand is uniformly distributed on a surface of the carrier, and the other end of the flexible chain ligand is coordinated on the transition metal.

2. The selective hydrogenation catalyst of claim 1, characterized in that the flexible chain ligand is a C.sub.2-C.sub.30 compound having at least one amine group or thiol group at both ends of the molecular chain.

3. The selective hydrogenation catalyst of claim 2, characterized in that the flexible chain ligand comprises one or more of ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, polyethyleneimine, methionine, cysteine, diphenyl sulfide and 2-fluorophenyl sulfide.

4. A preparation method of the selective hydrogenation catalyst of claim 1, characterized by comprising the following steps: (1) preparing a carrier: firstly, dispersing a carrier in water, and uniformly mixing to obtain a premix; then adding the flexible chain ligand into the premix, uniformly mixing, and performing hydrothermal reaction to obtain the flexible chain ligand modified carrier; (2) soaking the carrier prepared in the step (1) in a transition metal precursor solution for adsorption treatment; and (3) reducing the adsorbed material obtained in the step (2) to convert the transition metal precursor adsorbed on the surface of the carrier into a transition metal elementary substance.

5. The preparation method of claim 4, characterized in that the carrier is nitrogen-doped multi-stage porous carbon or one or more of oxides of Al, Ti, Zr, Ce, Mo, W, V, Mg, Ca, Mn, Fe, Zn, Ga, Ge, Sn, Y, Nb, La, Re and Si.

6. The preparation method of claim 4, characterized in that in step (2), the transition metal precursor in the transition metal precursor solution is one or more of PdCl.sub.2, Pd(acac).sub.2, H.sub.2PdCl.sub.4, Pd(NO.sub.3).sub.2, Pd(NH.sub.3).sub.4(NO.sub.3).sub.2, H.sub.2PtCl.sub.6, CuCl.sub.2, Ni(NO.sub.3).sub.2, IrCl.sub.3, and Ir(OAc).sub.3.

7. The preparation method of claim 4, characterized in that a molar ratio of the flexible chain ligand to the transition metal content in the transition metal precursor solution is 10-300.

8. The preparation method of claim 4, characterized in that the amount ratio of the flexible chain ligand to the carrier is 0.1-10 μL/mg.

9. The preparation method of claim 4, characterized in that the temperature of the hydrothermal reaction is 50-200° C. and the time of the hydrothermal reaction is 5-20 h.

10. The preparation method of claim 4, characterized in that the reduction treatment method is hydrogen reduction, formic acid reduction, hydrazine hydrate reduction or sodium borohydride reduction method.

11. A preparation method of the selective hydrogenation catalyst of claim 2, characterized by comprising the following steps: (1) preparing a carrier: firstly, dispersing a carrier in water, and uniformly mixing to obtain a premix; then adding the flexible chain ligand into the premix, uniformly mixing, and performing hydrothermal reaction to obtain the flexible chain ligand modified carrier; (2) soaking the carrier prepared in the step (1) in a transition metal precursor solution for adsorption treatment; and (3) reducing the adsorbed material obtained in the step (2) to convert the transition metal precursor adsorbed on the surface of the carrier into a transition metal elementary substance.

12. The preparation method of claim 11, characterized in that the carrier is nitrogen-doped multi-stage porous carbon or one or more of oxides of Al, Ti, Zr, Ce, Mo, W, V, Mg, Ca, Mn, Fe, Zn, Ga, Ge, Sn, Y, Nb, La, Re and Si.

13. A preparation method of the selective hydrogenation catalyst of claim 3, characterized by comprising the following steps: (1) preparing a carrier: firstly, dispersing a carrier in water, and uniformly mixing to obtain a premix; then adding the flexible chain ligand into the premix, uniformly mixing, and performing hydrothermal reaction to obtain the flexible chain ligand modified carrier; (2) soaking the carrier prepared in the step (1) in a transition metal precursor solution for adsorption treatment; and (3) reducing the adsorbed material obtained in the step (2) to convert the transition metal precursor adsorbed on the surface of the carrier into a transition metal elementary substance.

14. The preparation method of claim 13, characterized in that the carrier is nitrogen-doped multi-stage porous carbon or one or more of oxides of Al, Ti, Zr, Ce, Mo, W, V, Mg, Ca, Mn, Fe, Zn, Ga, Ge, Sn, Y, Nb, La, Re and Si.

15. An application of a selective hydrogenation catalyst in a catalytic hydrogenation reaction, characterized in that the selective hydrogenation catalyst serves as a catalyst in the selective hydrogenation reaction of alkynol, wherein a step of the catalytic hydrogenation reaction includes: feeding the selective hydrogenation catalyst, the alkynol, and hydrogen in a reaction kettle, wherein the selective hydrogenation catalyst comprises an active component and a carrier for supporting the active component, the active component is a transition metal particle, the carrier is modified by a flexible chain ligand in advance via a hydrothermal reaction, one end of the flexible chain ligand is uniformly distributed on a surface of the carrier, and the other end of the flexible chain ligand is coordinated on the transition metal; and the selective hydrogenation reaction of the alkynol is performed in the reaction kettle through the selective hydrogenation catalyst to form a hydrogenation product, wherein a temperature of the selective hydrogenation reaction is 20-90° C., and a pressure of the selective hydrogenation reaction is 0.5-5 MPa, wherein the flexible chain ligand comprises one or more of ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, polyethyleneimine, methionine, cysteine, diphenyl sulfide and 2-fluorophenyl sulphide.

16. The application of claim 15, characterized in that the alkynol is dehydrolinalool or 2-methyl-3-butyn-2-ol.

17. (canceled)

18. (canceled)

19. (canceled)

20. (canceled)

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0031] FIG. 1: a scanning electron microscope (SEM) photograph of the flexible chain modified nitrogen-doped porous carbon composite obtained in Example 1.

[0032] FIG. 2: a transmission electron microscopy (TEM) photograph of the flexible chain ligand modified Pd catalyst described in Example 1.

[0033] FIG. 3: a dark field scanning transmission electron microscope (STEM) photograph of the flexible chain ligand modified Pd catalyst described in Example 1.

[0034] FIG. 4: an x-ray energy dispersive spectrometer (EDS) spectra of the flexible chain ligand modified Pd catalyst described in Example 1.

[0035] FIG. 5: a diagram of a kettle type continuous hydrogenation device adopted by the present invention.

DESCRIPTION OF THE EMBODIMENTS

[0036] The technical solutions in the embodiments of the present invention will be described clearly and completely. Obviously, the described embodiments are part of the present invention, but not all of them. Based on the embodiments of the present invention, all other embodiments obtained by a person of ordinary skill in the art without involving any inventive effort are within the scope of the present invention.

[0037] The present invention provides a preparation method of a selective hydrogenation catalyst modified by a flexible chain ligand. The preparation method comprises the following steps:

[0038] (1) providing a flexible chain ligand modified carrier, wherein the flexible chain ligand is uniformly distributed on the surface of the carrier;

[0039] (2) dissolving the carrier modified by the flexible chain ligand in a transition metal precursor solution for adsorption treatment; and

[0040] (3) reducing the carrier subjected to adsorption treatment, so that the transition metal precursor adsorbed on the surface of the carrier is converted into a transition metal elementary substance, and an amine group or a sulfhydryl group at one end of the flexible chain is coordinated on the active component transition metal.

[0041] The preparation method of the flexible chain ligand modified carrier in step (1) specifically comprises the following steps:

[0042] Firstly, dissolving the carrier in water, and fully stirring to obtain a premix; then adding the flexible chain ligand to the premix, and subjecting the mixture to a hydrothermal reaction at 50-200° C. to provide the flexible chain ligand modified carrier.

[0043] The carrier is nitrogen-doped porous carbon or a metal oxide of one or more elements of Al, Ti, Zr, Ce, Mo, W, V, Mg, Ca, Mn, Fe, Zn, Ga, Ge, Sn, Y, Nb, La and Re.

[0044] The premix is a suspension and the carrier is insoluble in the solvent but uniformly distributed in the premix. Stirring is continued for 0.5-2 h during the mixing.

[0045] The ratio of the carrier to water is not limited, and further, the ratio of the mass of the carrier to the volume of water is (0.1 g-1 g):30 ml.

[0046] The flexible chain ligand is one or more of ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, polyethyleneimine, methionine, cysteine, diphenyl sulfide, and 2-fluorophenyl sulfide. Further, the flexible chain ligand is one or more of diethylenetriamine, triethylenetetramine, tetraethylenepentamine, diphenyl sulfide.

[0047] The reaction time of the hydrothermal reaction is 5-20 h, and further, the reaction time of the hydrothermal reaction is 10-20 h.

[0048] It will be appreciated that the hydrothermal reaction products need to be washed and dried prior to the adsorption treatment. The specific treatment process is as follows: filtering the hydrothermal reaction product, washing 3-5 times with a large amount of water and drying at a temperature of 60-100° C. for 6-12 h.

[0049] In the step (2), the loading amount (i.e. the mass fraction) of the transition metal in the flexible chain ligand modified selective hydrogenation catalyst can be regulated and controlled, and is not limited; specifically, it can be accomplished by adjusting the mass or molar amount of the transition metal precursor in the transition metal precursor solution.

[0050] The method for loading the transition metal on the flexible chain ligand modified carrier comprises the following steps:

[0051] dispersing the flexible chain ligand modified carrier in a transition metal precursor solution for adsorption treatment, wherein the adsorption reaction time is 5-15 hours, and further, the adsorption reaction time is 5-10 hours; and reducing the material subjected to adsorption treatment, so that a transition metal precursor adsorbed on flexible chain ligand modified carrier is converted into a transition metal elementary substance, and an amine group or a sulfhydryl group at one end of the flexible chain is coordinated on the active component transition metal.

[0052] In the hydrogen reduction process, the temperature is 50-500° C., the heating rate is 1-20° C./min, the time is 1-360 min, and the hydrogen flow rate is 20-200 ml/min.

[0053] The transition metal precursor in the transition metal precursor solution is one or more of PdCl.sub.2, Pd(acac).sub.2, H.sub.2PdCl.sub.4, Pd(NO.sub.3).sub.2, Pd(NH.sub.3).sub.4(NO.sub.3).sub.2, H.sub.2PtCl.sub.6, CuCl.sub.2, Ni(NO.sub.3).sub.2, IrCl.sub.3, and Ir(OAc).sub.3.

[0054] The molar ratio of the fed flexible chain ligand to the transition metal content in the transition metal precursor solution is 10-300.

[0055] The present invention also provides a novel flexible chain ligand modified selective hydrogenation catalyst which comprises an active component and a carrier for supporting the active component. The active component is a transition metal particle, the carrier is modified by a flexible chain ligand in advance, and the flexible chain ligand is uniformly distributed on the surface of the composite through hydrothermal reaction. The amine group or the sulfhydryl group at the other end of the flexible chain is directly coordinated on the active component transition metal, changing the electronic and spatial structures of the transition metal, and effectively improving the reaction performance of the flexible chain ligand modified catalyst for the selective hydrogenation reaction of alkynol. Meanwhile, the coordination interaction of the flexible chain ligand and the transition metal particle remarkably improves the stability of the catalyst.

[0056] The average particle size of the transition metal particles on the flexible chain ligand modified carrier is 0.5-5 nm. Preferably, the transition metal particles have an average particle size of 0.5-3 nm.

[0057] The mass fraction of the transition metal in the catalyst is 0.1-10%.

[0058] The present invention also provides an application of the transition metal catalyst modified by the flexible chain ligand in the catalytic hydrogenation reaction. The flexible chain ligand modified transition metal catalyst serves as a catalyst in the selective hydrogenation reaction of alkynol. The alkynol is one of dehydrolinalool and 2-methyl-3-butyn-2-ol. The hydrogenation equations for dehydrolinalool and 2-methyl-3-butyn-2-ol, respectively, are shown below.

##STR00001##

[0059] The amount of the transition metal in the catalyst is 0.2-1% of the mass of the alkynol.

[0060] The selective hydrogenation reaction temperature is 20-90° C., and the reaction pressure is 0.5-5 MPa.

[0061] The total residence time of the multi-kettles-in-series reaction kettle system is 120-480 minutes, the number of the multi-kettles in series is 2-4, and the volume of each reaction kettle can be equal or different. As shown in FIG. 5, a 4-kettles-in-series reaction kettle system is shown: the metering pump 1 is connected with the feeding position of the first reaction kettle 2; in the first to fourth reaction kettles 2-5, the discharge position of the previous reaction kettle is connected with the feed position of the next reaction kettle to form a series connection, wherein the feed position is arranged at the middle side line of the reaction kettle, and the discharge position is arranged at the upper side line of the reaction kettle; the upper ends of the first to fourth reaction kettles 2-5 are provided with air inlets respectively and are connected with the air inlet pipes 11-14 respectively; the discharging positions of the first to fourth reaction kettles 2-5 are respectively provided with overflow ports and filter elements 7-10; and the discharge position of the fourth reaction kettle 5 is connected with a storage tank 6.

[0062] The transition metal catalyst modified by flexible chain ligand of the present invention and their application are further illustrated by the following examples.

Example 1

[0063] 3 g of α-cellulose, 9 g of sodium bicarbonate, 9 g of ammonium oxalate were weighed, stirred thoroughly, transferred to a crucible, and calcined in a nitrogen furnace. The specific calcination process was as follows: maintaining at 30° C. for 30 min, increasing the temperature to 1,000° C. at a rate of 5° C./min, and calcining at 1,000° C. for 2 h; then, naturally lowering the temperature to room temperature. The calcined mixture was fully ground, washed with ultrapure water for three times, and dried at 70° C. overnight to obtain the nitrogen-doped graded porous carbon material.

[0064] 200 mg of nitrogen-doped graded porous carbon material were weighed, added with 30 ml of ultrapure water, and stirred for 10 minutes. 100 μL of diethylenetriamine was added and stirred for 30 min. Then, hydrothermal reaction was carried out at 150° C. for 10 h. The reaction product was naturally cooled to room temperature, filtered, washed with ultrapure water for three times, and dried at 70° C. overnight to obtain the flexible chain ligand modified nitrogen-doped porous carbon composite, namely the carrier.

[0065] 150 mg of flexible chain ligand modified nitrogen-doped porous carbon was weighed, added with 20 mL of ultrapure water, and added dropwise with 298 μL of 10 mg/mL PdCl.sub.2 solution slowly; the mixture was stirred for adsorption for 5 hours, filtered, washed for three times by using ultrapure water, and dried at 70° C. overnight. Hydrogen reduction was carried out at 300° C. for 2 h, (hydrogen flow rate: 50 mL/min, heating rate: 5° C./min) to obtain the flexible chain ligand modified Pd catalyst.

[0066] The nitrogen-doped porous carbon composite was subjected to a scanning electron microscope (SEM) test, and the results are shown in FIG. 1. As can be seen from FIG. 1, a rich pore structure can be clearly observed.

[0067] The flexible chain ligand modified Pd catalyst was subjected to transmission electron microscopy (TEM) test and dark field scan transmission electron microscopy (STEM) test, and the results are shown in FIGS. 2 and 3. As can be seen from FIGS. 2 and 3, the Pd particles are uniformly distributed on the surface of the flexible chain ligand modified nitrogen-doped porous carbon carrier.

[0068] The flexible chain ligand modified Pd catalyst was subjected to an X-ray energy dispersive spectrometer (EDS) analysis (note: X-ray EDS analysis is an experiment using X-rays to test the distribution state of elements). The result are shown in FIG. 4, and it can be seen that: the Pd element and the N element on the flexible chain ligand modified Pd catalyst are uniformly distributed, and at the same time, as can be seen in the second and third figures in FIG. 4, N and Pd are highly overlapped, thereby proving the effective coordination of the amine group with Pd.

[0069] The selective hydrogenation of 2-methyl-3-butyn-2-ol was carried out by two different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 6 L/h, the catalyst mass was 23.4 g, the reaction temperature was 70° C., and the reaction pressure was 1.5 MPa; and the volume of the second reaction kettle was 50 L, the catalyst mass was 117 g, the reaction temperature was 70° C., the reaction pressure was 1.5 MPa; the total residence time was 420 min, the conversion rate of 2-methyl-3-butyn-2-ol was 99.5%, and the selectivity of 2-methyl-3-buten-2-ol was 98.3%.

Example 2

[0070] 3 g of α-cellulose, 9 g of sodium bicarbonate, 9 g of ammonium oxalate were weighed, stirred thoroughly, transferred to a crucible, and calcined in a nitrogen furnace. The specific calcination process was as follows: maintaining at 30° C. for 30 min, increasing the temperature to 1,000° C. at a rate of 5° C./min, and calcining at 1,000° C. for 2 h; and then, naturally lowering the temperature to room temperature. The calcined mixture was fully ground, washed with ultrapure water for three times, and dried at 70° C. overnight to obtain the nitrogen-doped porous carbon material.

[0071] 200 mg of nitrogen-doped porous carbon material were weighed, added with 30 ml of ultrapure water, and stirred for 10 minutes. 20 μL of diethylenetriamine was added and stirred for 30 min. Then, hydrothermally reaction was carried out at 150° C. for 10 h. The reaction product was naturally cooled to room temperature, filtered, washed with ultrapure water for three times, and dried at 70° C. overnight to obtain the flexible chain ligand modified nitrogen-doped porous carbon composite.

[0072] 150 mg of flexible chain ligand modified nitrogen-doped porous carbon was weighed, added with 20 mL of ultrapure water, and added dropwise with 298 μL of 10 mg/mL PdCl.sub.2 solution slowly; the mixture was stirred for adsorption for 5 hours, filtered, washed for three times by using ultrapure water, and dried at 70° C. overnight. Hydrogen reduction was carried out at 300° C. for 2 h, (hydrogen flow rate: 50 mL/min, heating rate: 5° C./min) to obtain the flexible chain ligand modified Pd catalyst.

[0073] The flexible chain ligand modified Pd catalyst of Example 2 was prepared in essentially the same manner as in Example 1, except that 20 μL of diethylenetriamine was added during the hydrothermal reaction.

[0074] The selective hydrogenation of dehydrolinalool was carried out by two different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 7 L/h, the catalyst mass was 23.4 g, the reaction temperature was 70° C., and the reaction pressure was 1.0 MPa; the volume of the second reaction kettle was 50 L, the catalyst mass was 117 g, the reaction temperature was 70° C., the reaction pressure was 1.0 MPa; the total residence time was 360 min, the conversion rate of dehydrolinalool was 99%, and the selectivity of dehydrolinalool was 98.0%.

Example 3

[0075] 3 g of α-cellulose, 9 g of sodium bicarbonate, 9 g of ammonium oxalate were weighed, stirred thoroughly, transferred to a crucible, and calcined in a nitrogen furnace. The specific calcination process was as follows: maintaining at 30° C. for 30 min, increasing the temperature to 1,000° C. at a rate of 5° C./min, and calcining at 1,000° C. for 2 h; and then, naturally lowering the temperature to room temperature. The calcined mixture was fully ground, washed with ultrapure water for three times, and dried at 70° C. overnight to obtain the nitrogen-doped porous carbon material.

[0076] 200 mg of nitrogen-doped graded porous carbon material were weighed, added with 30 ml of ultrapure water, and stirred for 10 minutes. 40 μL of diethylenetriamine was added and stirred for 30 min. Then, hydrothermally reaction was carried out at 150° C. for 10 h. The reaction product was naturally cooled to room temperature, filtered, washed with ultrapure water for three times, and dried at 70° C. overnight to obtain the flexible chain ligand modified nitrogen-doped porous carbon composite.

[0077] 150 mg of flexible chain ligand modified nitrogen-doped porous carbon was weighed, added with 20 mL of ultrapure water, and added dropwise with 298 μL of 10 mg/mL PdCl.sub.2 solution slowly; the mixture was stirred for adsorption for 5 h, filtered, washed for three times by using ultrapure water, and dried at 70° C. overnight. Hydrogen reduction was carried out at 300° C. for 2 h, (hydrogen flow rate: 50 mL/min, heating rate: 5° C./min) to obtain the flexible chain ligand modified Pd catalyst.

[0078] The flexible chain ligand modified Pd catalyst of Example 3 was prepared in essentially the same manner as in Example 1, except that 40 μL of diethylenetriamine was added during the hydrothermal reaction.

[0079] The selective hydrogenation of 2-methyl-3-butyn-2-ol was carried out by a four different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 6 L/h, the catalyst mass was 23.4 g, the reaction temperature was 80° C., and the reaction pressure was 2 MPa; the volume of the second reaction kettle was 10 L, the catalyst mass was 23.4 g, the reaction temperature was 80° C., and the reaction pressure was 2 MPa; the volume of the third reaction kettle was 10 L, the catalyst mass was 23.4 g, the reaction temperature was 80° C., and the reaction pressure was 2 MPa; the volume of the fourth reaction kettle was 10 L, the catalyst mass was 23.4 g, the reaction temperature was 80° C., the reaction pressure was 2 MPa; the total residence time was 280 min, the conversion rate of 2-methyl-3-butyn-2-ol was 99.5%, and the selectivity of 2-methyl-3-butyn-2-ol was 98.2%.

Example 4

[0080] 200 mg of commercial alumina material was weighed, added with 30 ml of ultrapure water, and stirred for 10 min. 100 μL of diethylenetriamine was added and stirred for 30 min. Then, hydrothermally reaction was carried out at 150° C. for 10 h. The reaction product was naturally cooled to room temperature, filtered, washed with ultrapure water for three times, and dried at 70° C. overnight to obtain the flexible chain ligand modified alumina composite.

[0081] 150 mg of flexible chain ligand modified alumina was weighed, added with 20 mL of ultrapure water, and added dropwise with 298 μL of 10 mg/mL PdCl.sub.2 solution slowly; the mixture was stirred for adsorption for 5 hours, filtered, washed for three times by using ultrapure water, and dried at 70° C. overnight. Hydrogen reduction was carried out at 300° C. for 2 h, (hydrogen flow rate: 50 mL/min, heating rate: 5° C./min) to obtain the flexible chain ligand modified Pd catalyst.

[0082] The flexible chain ligand modified Pd catalyst of Example 4 was prepared in essentially the same manner as in Example 1, except that the carrier was commercial alumina.

[0083] The selective hydrogenation of dehydrolinalool was carried out by two different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 7 L/h, the catalyst mass was 23.4 g, the reaction temperature was 80° C., and the reaction pressure was 1.0 MPa; and the volume of the second reaction kettle was 50 L, the catalyst mass was 117 g, the reaction temperature was 80° C., the reaction pressure was 1.0 MPa; the total residence time was 360 min, the conversion rate of dehydrolinalool was 99.4%, and the selectivity of dehydrolinalool was 97.6%.

Example 5

[0084] The flexible chain ligand modified Pd catalyst of Example 5 was prepared in essentially the same manner as in Example 1, except that 100 μL of ethylenediamine was added during the hydrothermal reaction.

[0085] The selective hydrogenation of dehydrolinalool was carried out by two different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 7 L/h, the catalyst mass was 46.8 g, the reaction temperature was 75° C., and the reaction pressure was 1.0 MPa; the volume of the second reaction kettle was 50 L, the catalyst mass was 175 g, the reaction temperature was 75° C., the reaction pressure was 1.0 MPa; the total residence time was 360 min, the conversion rate of dehydrolinalool was 99.6%, and the selectivity of dehydrolinalool was 98.1%.

Example 6

[0086] The flexible chain ligand modified Pd catalyst of Example 6 was prepared in essentially the same manner as in Example 1, except that 100 μL of triethylenetetramine was added during the hydrothermal reaction.

[0087] The selective hydrogenation of 2-methyl-3-butyn-2-ol was carried out by four different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 6 L/h, the catalyst mass was 46.8 g, the reaction temperature was 70° C., and the reaction pressure was 2 MPa; the volume of the second reaction kettle was 10 L, the catalyst mass was 23.4 g, the reaction temperature was 70° C., and the reaction pressure was 2 MPa; the volume of the third reaction kettle was 10 L, the catalyst mass was 23.4 g, the reaction temperature was 70° C., and the reaction pressure was 2 MPa; the volume of the fourth reaction kettle was 10 L, the catalyst mass was 23.4 g, the reaction temperature was 70° C., the reaction pressure was 2 MPa; the total residence time was 280 min, the conversion rate of 2-methyl-3-butyn-2-ol was 99.5%, and the selectivity of 2-methyl-3-butyn-2-ol was 98.1%.

Example 7

[0088] The flexible chain ligand modified Pd catalyst of Example 7 was prepared in essentially the same manner as in Example 1, except that 100 μL of diphenyl sulfide was added during the hydrothermal reaction.

[0089] The selective hydrogenation of dehydrolinalool was carried out by two different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 7 L/h, the catalyst mass was 46.8 g, the reaction temperature was 75° C., and the reaction pressure was 1.0 MPa; and the volume of the second reaction kettle was 50 L, the catalyst mass was 175 g, the reaction temperature was 75° C., the reaction pressure was 1.0 MPa; the total residence time was 360 min, the conversion rate of dehydrolinalool was 99.6%, and the selectivity of dehydrolinalool was 98.1%.

Comparative Example 1

[0090] The selective hydrogenation catalyst was prepared essentially the same as in Example 1 except that no flexible chain ligand was added and no hydrothermal reaction was performed.

[0091] The selective hydrogenation of 2-methyl-3-butyn-2-ol was carried out by two different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 7 L/h, the catalyst mass was 23.4 g, the reaction temperature was 70° C., and the reaction pressure was 1.0 MPa; and the volume of the second reaction kettle was 50 L, the catalyst mass was 117 g, the reaction temperature was 70° C., the reaction pressure was 1.0 MPa; the total residence time was 360 min, the conversion rate of 2-methyl-3-butyn-2-ol was 70.4%, and the selectivity of 2-methyl-3-buten-2-ol was 32.5%.

Comparative Example 2

[0092] The selective hydrogenation catalyst was prepared essentially the same as in Example 1 except that no flexible chain ligand was added and no hydrothermal reaction was performed.

[0093] The selective hydrogenation of dehydrolinalool was carried out by two different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 7 L/h, the catalyst mass was 23.4 g, the reaction temperature was 70° C., and the reaction pressure was 1.0 MPa; the volume of the second reaction kettle was 50 L, the catalyst mass was 117 g, the reaction temperature was 70° C., the reaction pressure was 1.0 MPa; the total residence time was 360 min, the conversion rate of dehydrolinalool was 65.7%, and the selectivity of dehydrolinalool was 43.5%.

Comparative Example 3

[0094] The selective hydrogenation catalyst was prepared essentially the same as in Example 1 except 167 mg of o-phenanthroline was added during the hydrothermal reaction.

[0095] The selective hydrogenation of 2-methyl-3-butyn-2-ol was carried out by two different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 6 L/h, the catalyst mass was 23.4 g, the reaction temperature was 70° C., and the reaction pressure was 1.5 MPa; and the volume of the second reaction kettle was 50 L, the catalyst mass was 117 g, the reaction temperature was 70° C., the reaction pressure was 1.5 MPa; the total residence time was 420 min, the conversion rate of 2-methyl-3-butyn-2-ol was 46.8%, and the selectivity of 2-methyl-3-buten-2-ol was 75.4%.

Comparative Example 4

[0096] The selective hydrogenation catalyst was prepared essentially the same as in Example 1 except 167 mg of o-phenanthroline was added during the hydrothermal reaction.

[0097] The selective hydrogenation of dehydrolinalool was carried out by two different reaction kettles in series mode. The volume of the first reaction kettle was 10 L, the feed rate was 6 L/h, the catalyst mass was 23.4 g, the reaction temperature was 70° C., and the reaction pressure was 1.5 MPa; the volume of the second reaction kettle was 50 L, the catalyst mass was 117 g, the reaction temperature was 70° C., the reaction pressure was 1.5 MPa; the total residence time was 420 min, the conversion rate of dehydrolinalool was 38.5%, and the selectivity of dehydrolinalool was 77.0%.

[0098] The actual loading amounts of the transition metals in the catalysts obtained in the above Examples 1 to 7 and Comparative Examples 1 to 4 were measured by the atomic emission spectroscopy.

[0099] Table 1 below shows the raw materials, partial process parameters and catalytic hydrogenation effects of the selective hydrogenation catalysts used in Examples 1-7 and Comparative Examples 1-4 above.

TABLE-US-00001 TABLE 1 raw materials, partial process parameters and catalytic hydrogenation effects of the selective hydrogenation catalysts used in each example and comparative example. Molar ratio of Amount ratio flexible chain of flexible ligand to transition chain Transition Catalytic metal content in ligand to metal hydrogenation effects transition metal carrier, Partial process loading Raw material Selec- Nos Flexible chain ligands precursor solution μL/mg parameters amount conversion rates tivity Example 1 Diethylenetriamine, 55.30 0.5 Hydrothermal reaction 0.79% 2-Methyl-3- 98.3% 100 μL temperature: 150° C. butyn-2-ol, Hydrothermal reaction 99.5% time: 10 h Example 2 Diethylenetriamine, 11.06 0.1 Hydrothermal reaction 0.81% Dehydrolinalool, 98.0% 20 μL temperature: 150° C. 99% Hydrothermal reaction time: 10 h Example 3 Diethylenetriamine, 22.12 0.2 Hydrothermal reaction 0.8% 2-Methyl-3- 98.2% 40 μL temperature: 150° C. butyn-2-ol, Hydrothermal reaction 99.5% time: 10 h Example 4 Diethylenetriamine, 55.30 0.5 Hydrothermal reaction 0.8% Dehydrolinalool, 97.6% 100 μL temperature: 150° C. 99.4% Carrier: Hydrothermal reaction commercial alumina time: 10 h Example 5 Ethylenediamine, 89.17 0.5 Hydrothermal reaction 0.78% Dehydrolinalool, 98.1% 100 μL temperature: 150° C. 99.6% Hydrothermal reaction time: 10 h Example 6 Triethylenetetramine, 39.94 0.5 Hydrothermal reaction 0.74% 2-Methyl-3- 98.1% 100 μL temperature: 150° C. butyn-2-ol, Hydrothermal reaction 99.5% time: 10 h Example 7 Diphenyl sulfide, 35.59 0.5 Hydrothermal reaction 0.82% Dehydrolinalool, 98.1% 100 μL temperature: 150° C. 99.6% Hydrothermal reaction time: 10 h Comparative — — — — 0.84% 2-methyl-3- 32.5% Example 1 butyn-2-ol, 70.4% Comparative — — — — 0.84% Dehydrolinalool, 43.5% Example 2 65.7% Comparative O-Phenanthroline 55.30 — Hydrothermal reaction 0.75% 2-methyl-3- 75.4% Example 3 167 mg temperature: 150° C. butyn-2-ol, Hydrothermal reaction 46.8% time: 10 h Comparative O-Phenanthroline 55.30 — Hydrothermal reaction 0.75% Dehydrolinalool, 77.0% Example 4 167 mg temperature: 150° C. 38.5% Hydrothermal reaction time: 10 h

[0100] As can be seen from the data in Table 1 above, Examples 1-7 using the selective hydrogenation catalyst obtained by the preparation method of the present invention have higher conversions and selectivity in the catalytic hydrogenation of dehydrolinalool and 2-methyl-3-butyn-2-ol than Comparative Examples 1-4 without the catalyst obtained by the preparation method of the present invention.

[0101] Meanwhile, in order to verify that the selective hydrogenation catalyst obtained by the preparation method of the present invention can maintain high conversion rates and selectivity, i.e., has high stability, in a continuous hydrogenation reaction, the following examples and comparative examples were designed.

Examples 8-9, Comparative Examples 5-6

[0102] According to the method for selectively hydrogenating of 2-methyl-3-butyn-2-ol in Example 1, stability experiment comparison was carried out using the catalysts obtained in Example 1 and Comparative Example 1, respectively, and the results are shown in Table 2 below:

TABLE-US-00002 TABLE 2 Conversion rates and selectivity of different selective hydrogenation catalysts Continuous Sources of reaction Conversion Selec- Nos catalyst time, h rates, % tivity, % Example 8 Example 1 50 99.6 98.2 Example 9 Example 1 100 98.4 98.3 Comparative Comparative 50 60.2 30.2 Example 5 Example 1 Comparative Comparative 100 44.6 28.4 Example 6 Example 1

Examples 10-11, Comparative Examples 7-8

[0103] According to the method for selectively hydrogenating of dehydrolinalool in Example 2, stability experiment comparison was carried out using the catalysts obtained in Example 1 and Comparative Example 1, respectively, and the results are shown in Table 3 below:

TABLE-US-00003 TABLE 3 Conversion rates and selectivity of different selective hydrogenation catalysts after continuous hydrogenation of dehydrolinalool Continuous Sources of reaction Conversion Selec- Nos catalyst time, h rates, % tivity, % Example 10 Example 1 50 99.4 98.5 Example 11 Example 1 100 98.7 98.2 Comparative Comparative 50 45.7 58.4 Example 7 Example 1 Comparative Comparative 100 30.2 40.2 Example 8 Example 1

[0104] As can be seen from the above Tables 2 and 3, the reduction in conversion rate of Examples 8-9 and Examples 10-11 relative to Comparative Examples 5-6 and 7-8, respectively, indicates a certain loss of catalyst, while the catalyst of the present invention still maintain the conversion rate of more than 98% after continuously reacting for 100 h in the continuous hydrogenation reaction of 2-methyl-3-butyn-2-ol and dehydrolinalool, respectively. The loss rate is low, and after the selective hydrogenation catalyst is used for 100 hours of catalytic hydrogenation reaction. Although the active components of the catalyst are lost to a certain extent, the catalytic hydrogenation reaction still has higher selectivity of more than 98%, and the hydrogenation product can still be guaranteed to have higher quality, so that the selective hydrogenation catalyst obtained by the present invention has better stability.

[0105] The embodiments described above represent only a few embodiments of the present invention, the description of which is specific and detailed, but should not be construed to limit the scope of the present invention. It should be noted that several variations and modifications may be made by those skilled in the art without departing from the spirit of the present invention, which fall within the scope of the present invention. Therefore, the scope of the patent for invention shall be determined by the appended claims.