CN1298760A - Non-crystal catalyst for hydrogenating benzene and its preparing process - Google Patents
Non-crystal catalyst for hydrogenating benzene and its preparing process Download PDFInfo
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Abstract
The present invention relates to non-crystalline catalyst used in preparation of cyclohexane by bezene hydrogenation. Said catalyst is composed of (wt. ratio) nickel 1, boron 0.005-1.74, metallic additive M 0-30, porous carrier material L 0.42, M and L cannot be zero at the same time. Said nickel mainly is Ni-B or Ni-M-B non crystalline alloy, M is one or several of Cr, Mo, W, Fe, Co, Cu, L is one or several of porous inorganic oxide, active carbon, and one or several of molecular sieves. Said catalyst is obtained by removing inpurities after ions reduction, and possesses much higher benzene hydrogenation activity than conventional Raney nickel and Ni/gamma-Al2O3.
Description
The invention belongs to chemical technology field, is the new amorphous state Catalysts and its preparation method that is used for the prepared from benzene and hydrogen cyclohexane.
Cyclohexane is a kind of important organic synthesis intermediate, is the raw material of nylon-6, nylon-66 as it, by the cyclohexane important chemical material such as can also making phenol, cyclohexylamine of setting out.The whole world overwhelming majority's cyclohexane is all through this approach of benzene hydrogenation.In addition, in order to reduce the environmental pollution that the aromatic hydrocarbons imperfect combustion causes, European and American countries has been done strict restriction to the arene content in the fuel oil.So prepared from benzene and hydrogen cyclohexane process has economic worth and social effect.
In existing benzene hydrogenating catalyst, noble metal catalysts such as load type palladium, platinum, rhodium and ruthenium have very high benzene hydrogenation activity, but the cost height, and be easy to carbon deposit; The life-span of metal sulfide catalyst is long, but active low, and the operating condition harshness needs higher reaction temperature and pressure.Present industrial benzene hydrogenation prepares general nickel catalyst carried fixed bed gas-solid phase hydrogenation and the liquid phase outer circulation hydrogenation of adopting of cyclohexane, and catalytic efficiency is lower.There is the reaction focus that is difficult to overcome in the vapor phase method bed, limited production capacity, and have more side reaction to take place.The Raney Raney nickel that liquid phase method adopts traditionally owing to use a large amount of caustic soda extracting aluminium, causes serious environmental to pollute the problem that also exists catalyst mud to separate with product in the preparation.It is that catalyst, cyclohexane are that solvent carries out liquid-phase hydrogenatin that France IFP technology adopts diethyl adipic acid nickel, requires the sulfur content in the benzene to be lower than 1.5ppm, abandons primary first-order equation liquid, and pollutes in per six months.And the precipitation that generates behind the catalysqt deactivation causes wearing and tearing to the axial wood of circulating pump, and benzene leakage accident takes place when serious.Nanometer amorphous alloy has high selectivity and high activity because the surface has property, the undersaturated active sites of coordination such as a large amount of chemistry to catalytic reaction; Nano level particle diameter has been got rid of interior diffusion influence well, the catalytic efficiency height; Have certain anti-sulfur capacity concurrently, be expected to replace traditional industrial catalyst.
The objective of the invention is to propose a kind of catalytic efficiency height, eco-friendlyly be used for the amorphous alloy catalyst that the benzene catalytic hydrogenation prepares the novel nickeliferous and boron of cyclohexane, and propose this Preparation of catalysts method.
The catalyst that is used for the prepared from benzene and hydrogen cyclohexane provided by the invention is a kind of amorphous alloy catalyst of nickeliferous and boron, and it is made up of nickel, boron, metallic addition M and porous material carrier L, the weight of each component
Proportioning is as follows: the consumption with nickel is 1, and then the consumption of boron is 0.005～1.74, and the consumption of M is 0～30, and the consumption of L is 0～42, and M and L are not 0 simultaneously.Wherein, described nickel mainly exists with the form of Ni-B or Ni-M-B amorphous alloy; Described metallic addition M refers to can be by BH
4 -Ion is reduced to the metal of simple substance attitude one or more from corresponding ion, exists with the form of Ni-M-B amorphous alloy; The atomic ratio of nickel and boron is 1.0～6.0 in the described Ni-B amorphous alloy; In the described Ni-M-B amorphous alloy, (Ni+M) atomic ratio with boron is 3.0～10.0, and the atomic ratio of Ni and M is 0.8～1.2; Described nickel, boron and metallic addition M can load on the porous carrier materials L, also can individualism.
Preparation of catalysts method provided by the invention is in-20 ℃ to 100 ℃ temperature range, preferred 0 ℃ to 40 ℃, and under agitation with Ni
2+Ion and metallic addition M ion are from containing BH
4 -The aqueous solution reduction reaction of ion obtains described catalyst.Specifically be with a kind of load nickel salt, M salt porous carrier materials L or contain the mixed aqueous solution of nickel salt, M salt and molar concentration is 0.2～2.0 the BH that contains
4 -Ion solution is pressed 0.1～10.0 rate of charge haptoreaction; The load capacity of described nickel salt (in nickel ion weight) on porous carrier materials L is 0.1～20.0 heavy %; The load capacity of M ion on porous carrier materials L is 0～20.0 heavy %; When being unsupported catalyst, in the described mixed solution that contains nickel ion, M ion, the molar concentration of nickel ion, M ion is respectively 0.02～0.20,0.02～0.25.Among the described preparation method,, can be with BH to unsupported catalyst
4 -The aqueous solution of ion is added drop-wise in the aqueous solution of metal ion, also can be that the aqueous solution with metal ion is added drop-wise to BH
4 -In the aqueous solution of ion; To loaded catalyst, can be with BH
4 -On the aqueous solution of ion the has been added to load carrier L of metal ion, also can be that the aqueous solution with metal ion is added to and has flooded BH
4 -On the carrier L of ion, the two can be direct mixing, also can be slow adding, preferably adopts the mode that slowly adds, and near neutral, promptly gets catalyst provided by the invention with distilled water washing solid content.
Catalyst provided by the invention, its preferred ingredients weight proportion is: with nickel is 1, and then boron is 0.01～0.6, and M is 0～12, and porous carrier materials L is 0～18.
Ni of the present invention
2+Precursor be selected from nickel acetate, nickel chloride or nickelous sulfate, preferred nickel acetate or nickel chloride; BH
4 -The precursor of ion is selected from sodium borohydride or potassium borohydride.
Porous carrier materials L of the present invention refers to porous inorganic oxide, active carbon, in the molecular sieve one or more, described porous inorganic oxide refers to periodic table of elements II A family, group IIIA, IV A family, the oxide of IV B family element, wherein preferred silica, aluminium oxide, zirconia, titanium oxide, magnesia, in the calcium oxide one or more: described molecular sieve refers to various types of Si-Al molecular sieves, hetero-atom molecular-sieve, as A type molecular sieve, X type molecular sieve, Y zeolite, ZSM series molecular sieve, beta-molecular sieve, the Ω molecular sieve, phosphate aluminium molecular sieve, HTS etc., preferred porous carrier materials is a silica, aluminium oxide.
Described metallic addition M can be contained BH
4 -Ion solution is reduced to the metallic element of simple substance attitude one or more from corresponding salt, in the preferred elements periodic table in B family, II B-group, group VIB, the group VIII metal element one or more, in more preferred I B family, group VIB, the group VIII metal element one or more, metallic addition commonly used are one or more among Cr, Mo, W, Fe, Co, the Cu; The precursor of described M ion can be the M cation, also can be the acid radical anion that forms with oxygen element, and when being Fe, Cu, Co as M, the precursor of described M ion can be FeCl
2, FeSO
4, CuCl
2, CuSO
4, CoCl
2, Co (OAc)
2Deng; When M was Cr, Mo, W, the precursor of described M ion can be Na
2CrO
4, Na
2MoO
4, Na
2WO
4Deng.
According to catalyst provided by the invention, active component nickel all exists with the amorphous state form, and metallic addition M and Ni-B form amorphous alloy, exists with the form of Ni-M-B amorphous alloy.At this moment, ° locate a broad diffraction maximum (as shown in Figure 1) in 2 θ=45 on the X-ray diffraction spectrogram of measuring with CuK α target, be the characteristic diffraction peak of ni based amorphous alloy.Activity of such catalysts provided by the invention can be tested with the following method:
Intermittently investigate catalyst activity in the tank reactor at 0.5 liter of stainless steel.Benzene or certain density benzole soln, catalyst are put into still, and solvent can be alcohols, saturated alkane.Take a breath 3 times with the hydrogen of 2.2 MPa in autoclave sealing back, to remove the oxygen in the still.Be heated to constant hydrogen pressure after the reaction temperature behind preliminary filling hydrogen 2.2 MPa, reaction temperature is 50～200 ℃, more excellent 80～150 ℃, and hydrogen pressure 1～10 MPa, more excellent 3～10 MPa, and begin to stir, stir speed (S.S.) is greater than 1000 rev/mins.Take out response sample at interval with gas chromatographic analysis cyclohexane content, benzene content and other possible product content wherein with certain hour.
Fig. 1 is the typical X x ray diffraction spectrogram of prepared amorphous catalyst.
Specific embodiments of the invention: embodiment 1: the preparation of ultra-fine Ni-Co-B amorphous alloy catalyst
The freshly prepared 2.00 M potassium borohydride aqueous solution were at the uniform velocity splashed into nickel acetate (Ni (OAc) for 20 milliliters in 10 minutes
24H
2O, 0.25 M) and cobalt acetate (Co (OAc)
24H
2O, 0.25 M) in the mixed solution, mol ratio is B/Ni/Co=5/1/1.Reaction solution with ice-water bath constant temperature in 0 ℃ and in addition violent electromagnetic agitation, gained black precipitate centrifugation is washed till neutrality with distilled water, again promptly can be used for active testing behind the absolute ethanol washing, catalyst is designated as NCB, and the part characterization result of this catalyst is shown in table one.Embodiment 2: the preparation of ultra-fine Ni-Co-M-B (M=Cr, Mo, W) amorphous alloy catalyst
The freshly prepared 2.00 M potassium borohydride aqueous solution are splashed into nickel acetate (Ni (OAc)
24H
2O, 0.20 M), cobalt acetate (Co (OAc)
24H
2O, 0.20 M) and sodium tungstate (Na
2WO
42H
2O, 0.20 M) in the mixed solution, keeping the mol ratio of nickel acetate and cobalt acetate is 1, can obtain the different catalyst of W content by the adding volume that changes sodium tungstate solution, is designated as NCWB1, NCWB2, NCWB3.Mol ratio is fixed as B/ (Ni+Co+3W)=5/2 during reduction.Reaction solution with ice-water bath constant temperature in 0 ℃ and in addition violent electromagnetic agitation.Gained black precipitate centrifugation is washed till neutrality with distilled water, again promptly can be used for active testing behind the absolute ethanol washing.
The preparation method of ultrafine amorphous attitude alloy who contains molybdenum (catalyst is designated as NCMB1, NCMB2, NCMB3), chromium (catalyst is designated as NCCB1, NCCB2) is similar to the catalyst of tungstenic.Embodiment 3: support type Ni-Co-W-B/SiO
2The preparation of amorphous catalyst
With certain density Ni (OAc)
2, Co (OAc)
2(or its sulfate, hydrochloride) and Na
2WO
4Mixed solution dipping SiO
2Carrier, SiO
2Carrier boils with the 0.5 rare nitric acid that weighs % earlier before use and washes 2h, and after oven dry under 110 ℃ of infrared lamps was spent the night, 500 ℃ of roasting 2 h in Muffle furnace were crushed to 40～60 orders then again.Soaked carrier slowly splashes into the solution of potassium borohydride of 2.00 M after oven dry under 110 ℃ of infrared lamps is spent the night, and mol ratio is B/ (Ni+Co+3W)=5/2, and fixedly the mol ratio of nickel and cobalt is 1.Cool off with ice-water bath when being reflected at stirring.Catalyst is washed with distilled water to pH=7.3～7.8, can use for several times with absolute ethanol washing again, and the gained catalyst is designated as NCBS, NCWBS1, NCWBS2, NCWBS3, NCWBS4, NCWBS5, NCWBS6, and the catalyst member characterization result is shown in table two.Embodiment 4: support type Ni-B/ γ-Al
2O
3The preparation of amorphous catalyst
γ-Al
2O
3Boil with the 0.5 rare nitric acid that weighs % earlier and wash 2h, after oven dry under 110 ℃ of infrared lamps was spent the night, 500 ℃ of roasting 2 h in Muffle furnace were crushed to 40～60 orders then again.With a certain amount of nickel chloride aqueous solution (NiCl
24H
2O, 2.00M) behind the dipping, elder generation, dries down in 110 ℃ of infrared lamps and spends the night down to drying 70 ℃ of stirred in water bath.Under vigorous stirring, drip 2.00 M KBH during room temperature
4With the mixed aqueous solution of 0.20 M NaOH, the mol ratio of boron and nickel is 3 during reduction.Catalyst is washed till the pH value with distilled water and is about 7.0, and is standby with the washing of 99.5% ethanol then.By the increase of load capacity, catalyst is designated as NBA1, NBA2, NBA3, NBA4, NBA5 successively, and the part characterization result of this catalyst is shown in table three.
Another kind of Ni-B/ γ-Al
2O
3Outside directly oven dry was spent the night under 110 ℃ of infrared lamps after the Preparation of catalysts method was flooded divided by nickel chloride aqueous solution, consistent with top process conditions.Catalyst is designated as NBA6.Benzene hydrogenation activity test case 1: ultra-fine Ni-Co-B, Ni-Co-M-B (M=Cr, Mo, W) amorphous alloy
Catalyst amount is 1 gram, 75 milliliters of purified petroleum benzin, and 75 milliliters of 99.5% ethanol, 100 ℃ of reaction temperatures, Hydrogen Vapor Pressure 4.0MPa, 1000 rev/mins of stir speed (S.S.)s, hydrogenation the results are shown in table four.Benzene hydrogenation activity test case 2: the influence of solvent
Catalyst is selected NCWB2 for use, and solvent is respectively methyl alcohol, ethanol, butanols, isopentane, cyclohexane.All the other conditions are with benzene hydrogenation activity test case 1, and hydrogenation the results are shown in table five.Benzene hydrogenation activity test case 3: Temperature Influence
Catalyst is selected NCWB2 for use, and all the other conditions are with benzene hydrogenation activity test case 1, and hydrogenation the results are shown in table six.Benzene hydrogenation activity test case 4: support type Ni-Co-W-B/SiO
2Amorphous catalyst
Catalyst amount is 2.0g, purified petroleum benzin consumption 150ml, and 150 ℃ of reaction temperatures, Hydrogen Vapor Pressure 4.0MPa, 1000 rev/mins of stir speed (S.S.)s, hydrogenation the results are shown in table seven.Benzene hydrogenation activity test case 5: Temperature Influence
Catalyst is selected NCWBS2 for use, and all the other conditions are with benzene hydrogenation activity test case 4, and hydrogenation the results are shown in table eight.Benzene hydrogenation activity test case 6: support type Ni-B/ γ-Al
2O
3Amorphous catalyst
Catalyst amount is 1.0g, purified petroleum benzin consumption 200ml, and 100 ℃ of reaction temperatures, Hydrogen Vapor Pressure 4.0MPa, 1000 rev/mins of stir speed (S.S.)s, hydrogenation the results are shown in table nine.Benzene hydrogenation activity test reference examples 1:W-2 type Raney Raney nickel (preparation method see " Preparation of Catalyst handbook, tail is rugged, field portion is great third-class, Chemical Industry Press, Beijing, the 608th page, 1962).Except that adopting 1 gram W-2 type Raney Raney nickel, all the other conditions are with benzene hydrogenation activity test case 1, and hydrogenation the results are shown in table four.Benzene hydrogenation activity test reference examples 2: support type Ni/ γ-Al
2O
3Catalyst (preparation method sees J.Chem.Soc., Faraday Trans.1,81,2733,1985).Remove and adopt 1 gram support type Ni/ γ-Al
2O
3Outside the catalyst, all the other conditions are with benzene hydrogenation activity test case 4, and hydrogenation the results are shown in table nine.Benzene hydrogenation activity test reference examples 3: support type Ni-B/SiO
2Amorphous catalyst (the same NBA6 of preparation method, but carrier is SiO
2).Remove and adopt 1 gram support type Ni-B/SiO
2Outside the catalyst, all the other conditions are with benzene hydrogenation activity test case 4, and hydrogenation the results are shown in table nine.
By the result who obtains (table four is to table nine) as can be seen, the benzene hydrogenation activity of amorphous state NCMB catalyst series is 150% to 200% of a W-2 type Raney Raney nickel, and the benzene hydrogenation activity of NBA4 amorphous catalyst is about the Ni/ γ-Al that obtains with hydrogen reducing
2O
3500%, be Ni-B/SiO
2222%.For amorphous state NCMB catalyst series, higher benzene hydrogenation activity is arranged when being solvent with the product cyclohexane simultaneously, so just save the loaded down with trivial details product and the separating step of solvent, simplified operation and energy savings.For amorphous state NCWBS2 catalyst, in bigger range of reaction temperature, catalyst can both keep higher activity, has shown good operating flexibility.
The specific area of table one, amorphous state NCMB catalyst series, body phase and surface composition
| Catalyst | Specific area (m 2· -1) | Body phase composition (atomic ratio) | Surface composition (atomic ratio) |
| ??NCB ?NCWB1 ?NCWB2 ?NCWB3 | ????8.6 ????30.2 ????33.7 ????13.7 | Ni 41.4Co 42.4B 16.2Ni 44.8Co 43.9W 1.3B 10.0Ni 41.1Co 43.1W 2.7B 13.1Ni 40.5Co 42.6W 4.0B 12.9 | Ni 28.6Co 38.6B 32.8Ni 23.7Co 28.3W 1.9B 46.0Ni 28.2Co 33.1W 3.1B 35.6Ni 21.4Co 34.0W 4.5B 40.1 |
Table two, support type NiCoWB/SiO
2The part characterization result of catalyst series
| Catalyst | Body phase composition (atomic ratio) | Specific area (m 2/g) | Average pore size (_) |
| ????NCBS ????NCWBS1 ????NCWBS2 ????NCWBS3 ????NCWBS4 ????NCWBS5(C1 -) ????NCWBS6(SO 4 2-) | ??Ni 38.4Co 37.7B 23.9??Ni 37.2Co 36.7W 3.5B 22.6??Ni 37.1Co 36.1W 7.7B 19.2??Ni 35.7Co 35.2W 11.9B 17.2??Ni 35.9Co 34.8W 12.2B 17.7??Ni 38.8Co 38.5W 9.9B 12.8??Ni 37.9Co 38.0W 4.6B 19.4 | ????180.4 ????189.9 ????171.5 ????169.6 ????161.8 ????158.1 ????152.0 | ????56.8 ????63.6 ????62.1 ????67.4 ????68.2 ????70.3 ????71.8 |
Table three, support type Ni-B/ γ-Al
2O
3The part characterization result of amorphous catalyst
| Catalyst | Nickel loading (heavy %) | Body phase composition (atomic ratio) | Specific area (m 2·g -1) |
| ????NBA1 ????NBA2 ????NBA3 ????NBA4 ????NBA5 | ????2.4 ????5.6 ????7.1 ????9.6 ????11.8 | ????Ni 64B 36????Ni 64B 36????Ni 62B 38????Ni 63B 37????Ni 62B 38 | ????170.5 ????163.1 ????160.3 ????154.1 ????150.5 |
The benzene hydrogenation activity of table four, amorphous state NCMB catalyst series and W-2 type Raney Raney nickel
| Catalyst | ???? aConversion ratio (%) | ???? bSelectivity (%) |
| W-2 type Raney nickel NCB NCWB1 NCWB2 NCWB3 NCMB1 NCMB2 NCMB3 NCCB1 NCCB2 | ????44.7 ????67.5 ????87.1 ????～100 ????89.8 ????77.0 ????91.9 ????79.7 ????80.3 ????66.5 | ????100 ????100 ????100 ????100 ????100 ????100 ????100 ????100 ????100 ????100 |
a6 h benzene conversion ratios
bThe cyclohexane selectivity
Table five, solvent are to the influence of amorphous state NCWB2 catalyst benzene hydrogenation activity
| Solvent | Reaction time (min) | aConversion ratio (%) | bSelectivity (%) |
| Methanol n-butanol isopentane cyclohexane | ????360 ????360 ????210 ????90 ????90 | ????91.4 ????100 ????100 ????100 ????100 | ????100 ????100 ????100 ????100 ????100 |
aThe benzene conversion ratio
bThe cyclohexane selectivity
Table six, temperature are to the influence of amorphous state NCWB2 catalyst benzene hydrogenation activity
| Reaction temperature (℃) | ???? aConversion ratio (%) | ???? bSelectivity (%) |
| ????90 ????100 ????120 ????150 ????180 | ????82.0 ????～100 ????96.4 ????72.6 ????69.3 | ????100 ????100 ????100 ????100 ????100 |
a6 h benzene conversion ratios
bThe cyclohexane selectivity
Table seven, support type Ni-Co-W-B/SiO
2The benzene hydrogenation activity of amorphous catalyst
| Catalyst | ???? aConversion ratio (%) | ???? bSelectivity (%) |
| ????NCBS ????NCWBS1 ????NCWBS2 ????NCWBS3 ????NCWBS4 | ????76.8 ????82.2 ????93.4 ????54.0 ????48.5 | ????100 ????100 ????100 ????100 ????100 |
a6 h benzene conversion ratios
bThe cyclohexane selectivity
Table eight, temperature are to the influence of amorphous state NCWBS2 catalyst benzene hydrogenation activity
| Reaction temperature (℃) | ???? aConversion ratio (%) | ???? bSelectivity (%) |
| ????100 ????130 ????145 ????160 ????180 | ????-65.2 ????92.3 ????92.5 ????93.5 ????99.9 | ????100 ????100 ????100 ????100 ????100 |
a6 h benzene conversion ratios
bThe cyclohexane selectivity
Table nine, support type Ni-B/ γ-Al
2O
3Amorphous catalyst, Ni/ γ-Al
2O
3, Ni-B/SiO
2The benzene hydrogenation activity of catalyst
| Catalyst | A conversion ratio (%) | B selectivity (%) |
| ????Ni/γ-A1 2O 3????Ni-B/SiO 2????NBA4 ????NBA6 | ????18.7 ????42.9 ????95.2 ????68.8 | ????100???? ????100 ????100 ????100 |
a6 h benzene conversion ratios
bThe cyclohexane selectivity
Claims (11)
1. amorphous alloy catalyst that is used for the nickeliferous and boron of prepared from benzene and hydrogen cyclohexane, it is characterized in that it is made up of nickel, boron, metallic addition M and porous material L, the weight ratio of each component is: the consumption with nickel is 1, then the consumption of boron is 0.005～1.74, the consumption of M is 0～30, the consumption of L is 0～42, and M and L are not 0 simultaneously; Wherein nickel mainly exists with the form of Ni-B or Ni-M-B amorphous alloy, and metallic addition M is meant can be by BH
4 -Ion is reduced to the metal of simple substance attitude one or more from corresponding ion.
2. catalyst according to claim 1, it is characterized in that the weight proportion of each component is: with nickel is 1, and boron is 0.01～0.6, and metallic addition M is 0～12, and porous carrier materials L is 0～18.
3. according to claim 1 or 2 described catalyst, it is characterized in that described metallic addition M is selected from one or more in I B family, II B-group, group VIB, the group VIII metal element.
4. according to the described catalyst of claim 3, it is characterized in that described metallic addition M is selected from one or more among Cr, Mo, W, Fe, Co, Pt, Pd, the Cu.
5. according to claim 1 or 2 described catalyst, it is characterized in that described porous material L is selected from one or more in porous inorganic oxide, active carbon, the molecular sieve.
6. catalyst according to claim 5 is characterized in that described porous inorganic oxide is one or more in silica, aluminium oxide, zirconia, titanium oxide, magnesia, the calcium oxide.
7. catalyst according to claim 5 is characterized in that described molecular sieve is all kinds Si-Al molecular sieve, hetero-atom molecular-sieve.
8. one kind is used for prepared from benzene and hydrogen cyclohexane Preparation of catalysts method, it is characterized in that in-20 ℃ to 100 ℃ temperature range, under agitation with Ni
2+Ion and metallic addition M ion are to contain BH
4 -The aqueous solution reduction of ion.
9. Preparation of catalysts method according to claim 8 is characterized in that with a kind of load the porous carrier materials L of nickel salt, M salt or has contained the mixed solution of nickel salt, M salt and molar concentration is 0.2～2.0 BH
4 -Ion solution is pressed 0.1～10.0 ingredient proportion haptoreaction, and wherein the load capacity 0.1～20.0 of nickel salt on L weighs %, and the load capacity of M ion on L is 0～20.0 heavy %.
According to Claim 8 with 9 described method for preparing catalyst, it is characterized in that unsupported catalyst, can be with BH
4 -The aqueous solution of ion is added drop-wise in the aqueous solution of metal ion, also can be that the aqueous solution with metal ion is added drop-wise to BH
4 -In the aqueous solution of ion:, can be with BH to loaded catalyst
4 -On the aqueous solution of ion the has been added drop-wise to load carrier of metal ion, also can be that the aqueous solution with metal ion is added drop-wise to and has flooded BH
4 -On the carrier of ion.
11. with 9 described method for preparing catalyst, it is characterized in that described Ni according to Claim 8
2+The precursor of ion is selected from nickel acetate, nickel chloride or nickelous sulfate, BH
4 -The precursor of ion is selected from sodium borohydride or potassium borohydride, and the precursor of M ion can be the M cation, also can be the acid radical anion that forms with oxygen element.
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100348317C (en) * | 2006-04-24 | 2007-11-14 | 厦门大学 | Aromatic hydrocarbon hydrogenation catalyst and its preparation method |
| CN102600891A (en) * | 2012-02-15 | 2012-07-25 | 辽宁石油化工大学 | Catalyst for preparing para-aminophenol by performing nitrobenzene selective hydrogenation in non-acid medium |
| CN103952719A (en) * | 2014-03-28 | 2014-07-30 | 中国科学院物理研究所 | Catalyst used for preparation of hydrogen through water electrolysis, and preparation method thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU733712A1 (en) * | 1978-01-10 | 1980-05-15 | Казахский Химико-Технологический Институт | Catalyst for producing cyclohexane |
| CN1012814B (en) * | 1988-05-21 | 1991-06-12 | 中国石油化工总公司辽阳石油化纤公司 | Homogeneous catalyst of benzene hydrogenization |
-
2000
- 2000-06-08 CN CN00116412A patent/CN1094386C/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100348317C (en) * | 2006-04-24 | 2007-11-14 | 厦门大学 | Aromatic hydrocarbon hydrogenation catalyst and its preparation method |
| CN102600891A (en) * | 2012-02-15 | 2012-07-25 | 辽宁石油化工大学 | Catalyst for preparing para-aminophenol by performing nitrobenzene selective hydrogenation in non-acid medium |
| CN103952719A (en) * | 2014-03-28 | 2014-07-30 | 中国科学院物理研究所 | Catalyst used for preparation of hydrogen through water electrolysis, and preparation method thereof |
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