According to the present invention, a kind of chromium-free fluorination catalyst is provided, it comprises the zinc of active promotion amount or is loaded in aluminum oxide, the compound of the zinc on halogenation aluminum oxide or the oxo aluminum halide carrier.
According to the present invention, a kind of production method of fluorinated hydrocarbons also is provided, this method is included in the fluorination catalyst that defines in the preceding paragraph and exists to descend in gas phase with hydrocarbon or halohydrocarbon and hydrogen fluoride reaction.
Mixing in the catalyzer consumption of zinc is to determine like this, when zinc promotor is mixed aluminum oxide, halo aluminum oxide or oxo aluminum halide, will cause their active promotion.This consumption is very important, and this is because when comparing with the catalyst activity of the zinc promotor of mixing optimum quantity, the zinc promotor of mixing too many amount will cause the minimizing of catalyst activity, rather than increase.Therefore, have only when zinc promotor to exist, could produce best activity and promote with correct amount.
Be impregnated in the catalyzer and will depend on the surface-area of employed underlying carrier, particularly carrier, and depend on the employed method of this improved catalyzer of preparation to obtain the promoted zinc promotion of remarkable activity dosage.Yet for any specific carrier and method for preparing catalyst, the optimum amount of zinc promotor can be determined by simple normal experiment.Generally speaking, the consumption of zinc will be that about 0.5%-of catalyst weight is about 30% usually, preferably about 1.5%-about 25%.
The optimum amount that mixes zinc depends on the surface-area of catalyzer, and particularly the worksheet area of " the worksheet area of catalyzer " catalyzer is a surface-area of also using the measured catalyzer in hydrogen fluoride pre-treatment (as mentioned below) back in Preparation of Catalyst; Or if catalyzer carries out pre-treatment without hydrogen fluoride, the worksheet area of catalyzer is the surface-area after catalyzer is used to use hydrofluoric gas phase fluorination so, and the worksheet area of catalyzer can be about 10 to about 100m
2/ g is normally at the about 50m of about 10-
2/ g.When being about 50m according to surface-area
2The about 400m of/g-
2When the aluminum oxide of/g prepares this catalyzer, after preparation and pre-treatment, will obtain the catalyzer of worksheet area in the range of definition, this catalyzer can be about 50m according to surface-area
2The about 250m of/g-
2/ g, preferably about 150m
2/ g to 250m
2The raw alumina of/g prepares.
As mentioned above, the amount of mixing promotor in the catalyzer also depends on the Preparation of catalysts method that is adopted.The significant part that it is believed that catalyzer is to contain the surface of being located in the cationic carrier of zinc promotor on aluminum oxide, halo aluminum oxide or the zirconyl oxyhalides aluminium lattice, and the amount of so just lip-deep zinc promotor has been determined activity of such catalysts.For the catalyzer that makes by dipping, the active promoter action of per unit weight zinc promotor is usually above the catalyzer at non-surperficial position zinc-bearing accelerator by the additive method preparation.
As an example, by under the situation of the zinc that mixes of dipping on the alumina supporter, the surface-area of the aluminum oxide that the preparation catalyzer uses is 180m
2/ g, when the consumption of zinc is that about 0.5%-of catalyst weight is about 10%, it is about 6% to be preferably about 0.5%-, and it is about 4% to be more preferred from about 1.5%-,, will produce best active promoter action at particularly at about 1.5%-about 3.5% o'clock.Be less than the zinc deficiency of 0.5% weight so that catalyzer produces significant promoter action, and more than the zinc of about 8% weight, then the active promoter action that provides in the zinc of above-mentioned optimum range is compared, and can not produce the remarkable increase of catalyst activity.As going out, under the situation of the catalyzer by prepared by co-precipitation, wherein, a large amount of zinc is impregnated in non-surperficial position, and the consumption of zinc is that about 3%-of catalyst weight is about 30%, and it is about 25% to be preferably about 4%-, particularly about 5%-about 15%.
Zinc promotor can compound form mix in the catalyzer, said compound is for for example at least at the halogenide that to a certain degree depends on employed catalyst preparation process, oxyhalogenide, oxide compound or oxyhydroxide.For by impregnated alumina, during the occasion of halo aluminum oxide or zirconyl oxyhalides alumina supporter, this compound is water-soluble salt preferably in Preparation of catalysts, halogenide for example, and nitrate or acetate, and use with its aqueous solution.The promotor of oxyhydroxide and aluminium can carry out co-precipitation, convert oxide compound subsequently to, with the preparation catalyzer.The mixing of insoluble zn cpds and basic catalyzer and mill a kind of Preparation of catalysts method also is provided comprises based on the Preparation of catalysts method of zirconyl oxyhalides aluminium: promoter compound is added to the hydration aluminum fluoride, and calcine this mixture.
Above-mentioned any method or other method all can be used to prepare zinc of the present invention and promote catalyzer.
Fluorination catalyst will stand the hydrogen fluoride and the pre-fluoridation of inert thinner not necessarily usually before being used for the catalyzer of fluoridation.Common pre-treatment comprise with catalyzer with hydrogen fluoride or hydrogen fluoride with heat in 250 ℃-450 ℃ under air mixture contacts.Therefore, can believe that the work catalyzer is that partially fluorinated zinc is loaded on the fluorizated aluminum oxide or on the fluorine alumina at least.
For for the use of fixed bed or fluidized-bed, ball that catalyzer can appropriate size or particulate form are used.It can by in air in about 300 ℃-Yue 500 ℃ temperature heat and periodically regeneration or reactivate.Air can mix use with inert gas such as nitrogen, or mixes use with hydrogen fluoride, and hydrogen fluoride will produce heat from the treating processes of catalyzer, and it can be directly used in the gas phase fluorination processing.
Substantially (not promoted) aluminum oxide, the activity of halo aluminum oxide or zirconyl oxyhalides Al catalysts increases by mixing promotor.By this catalyzer, by 1-chloro-2,2,2-Halothane and hydrogen fluoride production 1,1,1, the selectivity of the catalyzed reaction of 2-Tetrafluoroethane at least can be the same high with the not promoted accordingly catalyzer of use, usually will be greater than 85%.
Talk about if desired, this catalyzer can contain one or more metals in addition that dezincifies, for example, and nickel, copper, manganese, cobalt and iron; Particularly iron, cobalt and copper.This is because the existence of one or more these metals can strengthen the recovery extent that makes catalyst activity by the regeneration of catalyzer.When particularly preferred zinc loaded, we Chang Youxuan uses only zinc, or is mainly zinc at least, only contained a small amount of other metal, for example was less than 2.0% weight, preferably was less than 1.5% weight, particularly was less than other metal of 1.0% weight.Heat and, this catalyzer contains much more relatively zinc and loads, for example, and for example in the occasion of the catalyzer that makes by dipping, the zinc loading capacity will be greater than about 3%, be preferably greater than about 4%, particularly greater than about 5%, beyond the dezincification, we especially preferably mix a spot of iron, for example to can be about 0.1%-of catalyst weight about 2% for the incorporation of iron, and preferably about 0.1%-is about 1.5%, better about 0.5%-about 1.5%.Be preferably about 80: 1 to 2: 1, more preferably about 16: 1 to about 2: 1 based on the zinc of catalyzer percent by weight and the ratio of iron.Preferred this ratio is irrelevant with the absolute magnitude of zinc in catalyzer and iron.
Therefore, though the absolute magnitude of zinc and iron can be higher, for example with respect to catalyst weight at least 6%, preferred at least 10% zinc, and about 0.2-is about 12%, and the iron of preferably about 0.4-about 4.5% is for the catalyzer that for example makes by coprecipitation method, to cause a large amount of and zinc and iron are impregnated in the outer surface portions of catalyzer, but the relative quantity that is based on the zinc of weight percent of catalyst and iron is still preferably in the above-mentioned scope that provides.
Of the present inventionly be further characterized in that the application of promoted catalyzer in fluorination process, fluorination process comprises that hydrocarbon or halohydrocarbon and hydrogen fluoride react in gas phase.
Alkene (unsaturated hydrocarbons), particularly haloolefin, for example preferred C that contains a chlorine atom at least
1-4Haloolefin can fluoridize; Can carry out the fluorizated object lesson is by 1-chloro-2,2, and the 2-Halothane produces 1,1,1, and the 2-Tetrafluoroethane is produced 1-chloro-2,2 by trieline, 2-Halothane and with 1-chloro-2, and the 2-difluoroethylene converts 1-chlorine 2,2 to, the 2-Halothane.The example of the fluoridation that other this catalyzer is suitable for is that tetrachloroethylene and hydrogen fluoride are produced dichlorotrifluoroethane (123) in gas-phase reaction, one chloro-tetrafluoroethane (124) and/or pentafluoride ethane (125), produce Refrigerant R 113 (113) in gas-phase reaction, a dichloro tetrafluoro ethane (114/114a) and/or a chloropentafluoroethane (115) with tetrachloroethylene and chlorine and hydrogen fluoride.
When using chromic oxide or halo chromic oxide as catalyzer, employed fluorination conditions can be known spendable those conditions; For example, depend on the specific fluoridation of being carried out, can be with normal atmosphere or super-atmospheric pressure, the temperature of hydrogen fluoride and 180 ℃ to 500 ℃.
Yet the activity that promoted catalyzer increases makes reaction to use under inefficent loss to compare not promoted aluminum oxide to reach under the low significantly temperature of the required temperature of same activity to carry out.For example, when using not promoted oxidation companion, use 360 ℃ of relatively-high temperatures or higher, under normal atmosphere, by 1-chloro-2,2, the 2-Halothane generates 1,1,1, the productive rate of 2-Tetrafluoroethane only is 0.5%, and uses the promoted aluminum oxide of zinc just to be enough to the reaction efficiency that reaches bigger at for example 280 ℃ low temperature.If in other words temperature of reaction is identical, be 300 ℃ for example, when using promoted catalyzer, need the time of contact shorter.
The preferred concrete example of the inventive method is 1,1,1, the preparation method of 2-tetrafluoroethylene, this method comprises: in the presence of promoted catalyzer of the present invention, with 1-chloro-2,2,2-Halothane and hydrogen fluoride gas phase are reacted, and this method can be carried out in about 280 ℃-500 ℃ under normal atmosphere or super-atmospheric pressure.
This method can be the step in two-step approach or the three-step approach, and for example, it can be to produce 1,1 by trieline, 1, in second step of the method for 2-Tetrafluoroethane, the first step is trieline and the gas phase fluorination of hydrogen fluoride in the presence of fluorination catalyst, to produce 1-chloro-2,2,2-Halothane.Promoted catalyzer of the present invention can be used for the first step and second step of this two-step approach.The reaction conditions commonly used of the first step is normal atmosphere or super-atmospheric pressure and about 180 ℃-Yue 400 ℃ temperature.
By 1-chloro-2,2, the 2-Halothane produces 1,1,1, and the 2-Tetrafluoroethane contains poisonous impurity 1-chloro-2 with generation, the product stream of 2-difluoroethylene.This impurity can for example react it and hydrogen fluoride and remove in gas phase under 150 ℃-270 ℃ by be lower than about 270 ℃ in the presence of fluorination catalyst.Promoted catalyzer of the present invention can be used for this reaction.So the invention provides by the trieline preparation does not have 1-chloro-2 substantially, 1,1,1 of 2-difluoroethylene, three one-step preparing methods of 2-Tetrafluoroethane, wherein promoted catalyzer is used in a step or two steps or the reaction of per step.
Above-mentioned prepares 1,1,1 by trieline, and the particularly preferred concrete example of the two-step preparation of 2-Tetrafluoroethane comprises following steps:
(A) with 1-chloro-2,2,2-Halothane and carbon hydrogen fluoride mixture and fluorination catalyst contact in first reaction zone in about 280 ℃-Yue 450 ℃, contain 1,1,1 with formation, the product of 2-Tetrafluoroethane and hydrogenchloride and unreacting material.
(B) second reaction zone that the product and the trieline of step (A) are delivered to the fluorinated catalyzer, the temperature in this district is about 180 ℃ to about 400 ℃, but is lower than the temperature in the step (A), contains 1-chloro-2 with formation, 2, the 2-Halothane, 1,1,1, the 2-Tetrafluoroethane, hydrogenchloride and unreacted trieline and hydrofluoric product
(C) product of treatment step (B), with from 1-chloro-2,2, the 2-Halothane is isolated hydrogenchloride and 1,1,1 in unreacted hydrogen fluoride and the unreacted trieline, the 2-Tetrafluoroethane,
(D) with the 1-chloro-2,2 that obtains in the step (C), 2-Halothane and hydrogen fluoride are delivered to the said first reaction zone step (A) together, and wherein, chromium-free fluorination catalyst is used in a step (A) and a step (B) at least as the aforementioned.
In the step (A) of preferred concrete example, use the hydrogen fluoride that is at least stoichiometric quantity usually, consumption is every mole of 1-chloro-2,2 usually, 2-Halothane 1-10 mole, preferred 1-6 mole.Therefore, remove 1,1,1,2-Tetrafluoroethane, hydrogenchloride and beyond product, this reactions steps contains unreacted hydrogen fluoride usually.The preferable reaction temperature that is used for this step of this method is 325 ℃-385 ℃, and be 1-100 the duration of contact under the 5-20 bar pressure, preferred 5-30 second.
In step (B), every mole of trieline often uses 10-100, the hydrogen fluoride of preferred 15-60 mole.Therefore, the reaction product in this step also will contain unreacted hydrogen fluoride.Can be with 1 to 100 second, the duration of contact of preferred 5-30 second, temperature is generally 220 ℃ to 350 ℃, and pressure often clings to for 5-20.
The method according to this invention comprises preferred concrete example, preferably operate continuously, yet, in actual applications, the one-tenth activation of catalyzer.The periodic regeneration of essential catalyzer or reactivate interrupt the operate continuously of this method possibly.In this method operating period, can be to catalyzer supply air to the deactivation of anticatalyst, and reduce the frequency that interrupts this method owing to catalyst regeneration or reactivate.
To further illustrate the present invention by following example, but limit the present invention anything but.
Embodiment 1-7
With the 4.79g diameter is that 0.5-1.4mm, surface-area are 180m
2The particulate alumina of/g (being provided by Harshaw Ltd) adds in zinc chloride (0.21g) aqueous solution in 10ml distilled water, and stirs to guarantee that solid is by the solution complete wetting.Then by direct heating with this mixture drying, and the solid that generates sieved, to be given in the final granules of catalyst that the particle diameter that contains about 2.0%w/w zinc on the aluminum oxide is 0.5-1.4mm.Repeat above-mentioned steps, only be to use the liquor zinci chloridi that increases concentration, in final catalyzer, contain high final catalyzer to 6.6%w/w zinc to produce.Use the normal atmosphere microreactor to measure the activity of fluoridizing of the promoted aluminum oxide of zinc.The 2g catalyzer is packed in the microreactor of 1/4 inch diameter, and be controlled under the HF air-flow in 300 ℃ 1 hour, be heated to 350 ℃ then, and further be controlled under air/HF (ratio 1: 20) air-flow about 15 hours.
Then, be 1.0: 3.5 blended 1-chloro-2,2 with the mole feed molar ratio, 2-Halothane (133a) and HF contacted for 2 seconds to the microreactor feed at 300 ℃.
In order to compare, also tested the not promotes oxidn aluminium that is used for preparing promoted aluminum oxide.
Result of study is with 1,1,1, and the percentage yield of 2-Tetrafluoroethane is listed in the table 1, and shows, zinc is added in the aluminum oxide, and for 1,1,1, the yield increase of 2-Tetrafluoroethane (134a) has useful effect.
During at the about 3%w/w of about 2%-, the activity of the aluminium oxide catalyst of zinc dipping reaches the peak at zinc content.
Table 1
Embodiment | Catalyzer | Temperature of reaction (℃) |
1 2 3 4 5 6 7 | 0.5%Zn-Al
2O
3 1.0%Zn-Al
2O
3 2.0%Zn-Al
2O
3 2.2%Zn-Al
2O
3 3.0%Zn-Al
2O
3 4.4%Zn-Al
2O
3 6.6%Zn-Al
2O
3 | 360 | 350 | 340 | 330 | 320 |
6.3 7.5 20.1 - 18.7 13.6 10.6 | 4.3 5.5 17.2 16.5 15.1 9.4 8.1 | 1.96 3.27 11.3 11.0 11.2 6.6 6.3 | - - - 7.4 - - - | - - - 4.9 - - - |
Comparative example | Al
2O
3 | 0.25 | 0.15 | 0.09 | - | - |
Embodiment 8
Is 180m with the 4.39g particle diameter for the 0.5-1.4mm surface-area
2The particulate alumina of/g (being provided by Harshaw Ltd) adds to Nickel dichloride hexahydrate (II) in 5ml distilled water (0.41g) and in the aqueous solution of zinc chloride (0.21g), and stirs to guarantee that solid is by the solution complete wetting.Then by this mixture of direct drying, and the solid that generates being sieved, is the final granules of catalyst of 0.5-1.4mm with the particle diameter that obtains containing about 2.0%w/w zinc and about 2%w/w nickel on aluminum oxide.
According to the step of embodiment 1-7, under atmospheric pressure this catalyzer of 2g is tested.
In order to compare, also to measuring according to the activity of such catalysts that on aluminum oxide, contains 2% and 3.8% weight nickel of aforesaid nickelous chloride (II) aqueous solution preparation.The atom of 3.8% nickel on the aluminium oxide catalyst load with the catalyzer that contains 2% zinc and 2% nickel on identical.
Result of study is with 1,1,1, and the percentage yield of 2-Tetrafluoroethane is listed in the table 2, and show that compare with aluminum oxide is only arranged, zinc/nickel is added to aluminum oxide beneficial effect, although as than, compare with independent interpolation zinc, the interpolation effect of zinc/nickel is poor, even also poorer than the effect of adding nickel separately.
Table 2
Embodiment | Catalyzer | Temperature of reaction (℃) |
8 | 2%Zn/2%Ni-Al
2O
3 | 340 330 320 310 300 |
6.4 5.1 3.6 2.7 1.9 |
Comparative example | 2%Ni-Al
2O
3 | 3.1 2.3 1.6 1.1 0.7 |
Comparative example | 3.8%Ni-Al
2O
3 | 2.6 1.8 1.3 0.8 0.5 |
Embodiment 9
Is 180m with the 4.39g particle diameter for the 0.5-1.4mm surface-area
2The particulate alumina of/g (Harshaw Ltd provides) adds to cobalt chloride hexahydrate (II) in 5ml distilled water (0.404g) and in the aqueous solution of zinc chloride (0.21g), and stirs to guarantee that solid is by the solution complete wetting.Then by direct heating with this mixture drying, and the solid that obtains sieved contain 2.0%w/w zinc on the aluminum oxide and the 2%w/w cobalt button directly is the final granules of catalyst of 0.5-1.4mm to be given in.
Step according to embodiment 1-7 is under atmospheric pressure tested this catalyzer of 2g.
For relatively, also to measuring according to the activity of such catalysts that on aluminum oxide, contains 2%3.8% weight cobalt of cobalt chloride (II) aqueous solution preparation of crossing as mentioned above.The atom of 3.8% cobalt on the aluminium oxide catalyst load with the catalyzer that contains 2% zinc and 2% cobalt on identical.
Result of study is with 1,1,1, and the percentage yield of 2-Tetrafluoroethane is listed in the table 3, and show that compare with aluminum oxide is only arranged, zinc/cobalt is added to aluminum oxide beneficial effect, however, compare with independent interpolation zinc, the interpolation effect of zinc/cobalt is poor, even also poorer than the effect of adding cobalt separately.
Table 3
Embodiment | Catalyzer | Temperature of reaction (℃) |
9 | 2%Zn/2%Co-Al
2O
3 | 340 330 320 310 300 |
10.9 7.0 5.6 3.6 2.8 |
Comparative example | 2%Co-Al
2O
3 | 3.8 2.6 1.5 1.0 0.5 |
Comparative example | 3.8%Co-Al
2O
3 | 3.4 2.5 1.8 1.3 0.9 |
Embodiment 10
Is 180m with the 4.43g particle diameter for the 0.5-1.4mm surface-area
2The particulate alumina of/g (Harshaw Ltd provides) adds to four hydration Manganous chloride tetrahydrates (II) in the 5ml distilled water (0.36g) and in the aqueous solution of zinc chloride (0.21g), and stirs to guarantee the solid solution complete wetting.Then by direct heating with this mixture drying, and the solid that obtains sieved contain 2.0%w/w zinc on the aluminum oxide and 2%w/w manganese particle diameter is the final granules of catalyst of 0.5-1.4mm to be given in.
According to the step of embodiment 1-7, under atmospheric pressure this catalyzer of 2g is tested.
In order to compare, also to measuring according to the activity of such catalysts that on aluminum oxide, contains 2% and 3.68% weight manganese of aforesaid Manganous chloride tetrahydrate (II) aqueous solution preparation.The atom of 3.68% manganese on the aluminium oxide catalyst load with the catalyzer that contains 2% zinc and 2% manganese on identical.
Result of study is with 1,1,1, and the percentage yield of 2-Tetrafluoroethane is listed in the table 4, and show that compare with aluminum oxide is only arranged, zinc/manganese is added to aluminum oxide beneficial effect, however, compare with independent interpolation zinc, the interpolation effect of zinc/manganese is poor, even also poorer than the effect of adding manganese separately.
Table 4
Embodiment | Catalyzer | Temperature of reaction (℃) |
10 | 2%Zn/2%Mn-Al
2O
3 | 340 330 320 310 |
10.5 7.7 6.7 4.5 |
Comparative example | 2%Mn-Al
2O
3 | 1.0 0.7 0.4 0.3 |
Comparative example | 3.68%Mn-Al
2O
3 | 0.6 0.5 0.3 0.2 |
Embodiment 11-20
Is 180m with the 4.30g particle diameter for the 0.5-1.4mm surface-area
2The particulate alumina of/g (Harshaw Ltd provides) adds to iron(ic) chloride (III) in 10ml distilled water (0.07g) and in the aqueous solution of zinc chloride (0.63g), and stirs to guarantee that solid is by the solution complete wetting.Then by direct heating with this mixture drying, and the solid that obtains sieved contain 6.0%w/w zinc on the aluminum oxide and 0.5%w/w iron, particle diameter are the final granules of catalyst of 0.5-1.4mm to be given in.Except the iron(ic) chloride (III) and liquor zinci chloridi that use different concns, repeat above-mentioned steps, to provide the zinc of listing in table 5 and the final catalyzer of iron loading.
Under atmospheric pressure getting each 2g of these catalysis according to the step of embodiment 1-7 tests.
In order to compare, also to measuring according to the activity of such catalysts that on aluminum oxide, contains 2% weight iron of iron(ic) chloride (III) aqueous solution preparation as mentioned above.The atom of 6%w/w zinc and 0.5%w/w iron loads the atom equal to go up at aluminium oxide catalyst (embodiment 7) 6.6%w/w zinc and loads on aluminum oxide, for compare also the activity of such catalysts of embodiment 7 and embodiment 3,5 and 6 is listed in below.
Result of study is with 1,1,1, and the percentage yield of 2-Tetrafluoroethane is listed in the table 5, and shows, with independent iron or separately the interpolation of zinc compare, high relatively zinc load and zinc than iron ratio greater than 2: 1 times, zinc/iron adds to aluminum oxide beneficial effect.
Table 5
Embodiment | Catalyzer | Temperature of reaction (℃) |
11 12 13 14 15 16 17 18 19 20 | 2%Zn/1%Fe-Al
2O
3 2%Zn/2%Fe-Al
2O
3 3%Zn/1%Fe-Al
2O
3 3%Zn/2%Fe-Al
2O
3 3%Zn/3%Fe-Al
2O
3 3%Zn/5%Fe-Al
2O
3 4%Zn/1%Fe-Al
2O
3 4%Zn/2%Fe-Al
2O
3 6%Zn/0.5%Fe-Al
2O
3 6%Zn/1.5%Fe-Al
2O
3 | 360 | 350 | 340 | 330 | 320 |
13.2 13.9 19.3 16.0 10.9 9.8 13.4 12.2 13.4 | 11.6 10.5 16.3 12.8 9.4 8.9 12.4 8.9 13.7 13.4 | 8.9 8.5 10.9 9.7 6.9 6.9 9.9 7.7 9.9 9.4 | - - - 7.6 - - - 5.9 6.5 8.5 | - - - - - - - - 4.5 5.4 |
Comparative example 3567 | 2%Fe-Al
2O
3 2%Zn-Al
2O
3 3%Zn-Al
2O
3 4.4%Zn-Al
2O
3 6.6%Zn-Al
2O
3 | 1.0 20.1 18.7 13.6 10.6 | 0.6 17.2 15.1 9.4 8.1 | - 11.3 11.2 6.6 6.3 | - - - - - | - - - - - |
Embodiment 21-25
Following embodiment shows, with test button that zinc is used in combination in, have zinc only and provided than on aluminium oxide catalyst, containing the bigger active catalyzer of 6.6% weight zinc with the sample of iron.
Except that the solution that adds to aluminum oxide is as described below, prepare catalyzer according to the described method of previous embodiment 1-12:
Embodiment 21: identical with embodiment 12.
Embodiment 22:4.07g aluminum oxide adds to the ZnCl in 10ml water
2(0.63g) and CoCl
2In the aqueous solution of hexahydrate (0.3g).
Embodiment 23:4.07g aluminum oxide adds to the ZnCl in 10ml water
2(0.63) and NiCl
2In the aqueous solution of hexahydrate (0.3g).
Embodiment 24:4.04g aluminum oxide adds to the ZnCl in 10ml water
2(0.63g) and Mn (CH
3CO
2)
2In the aqueous solution of tetrahydrate (0.34g).
Embodiment 25:4.17g aluminum oxide adds to the ZnCl in 10ml water
2(0.63g) and CuCl
2In the aqueous solution of dihydrate (0.2g).
According to the step of embodiment 1-7, under normal atmosphere, get each 2g of these catalyzer and test.
Result of study is with 1,1,1, and the percentage yield of 2-Tetrafluoroethane is listed in the table 6, and the result shows, adds to aluminum oxide with any other metal with zinc and compares, and zinc/iron adds to aluminum oxide beneficial effect.
Table 6
Embodiment | Catalyzer | Temperature of reaction (℃) |
21 22 23 24 25 | 6%Zn/1.5%Fe-Al
2O
3 6%Zn/1.5%Co-Al
2O
3 6%Zn/1.5%Ni-Al
2O
3 6%Zn/1.5%Mn-Al
2O
3 6%Zn/1.5%Cu-Al
2O
3 | 350 | 340 | 330 | 320 |
13.4 5.5 5.1 4.7 3.5 | 9.4 4.7 3.4 3.7 3.0 | 8.5 3.2 2.8 2.5 2.3 | 5.4 2.8 1.7 - - |
Comparative example | 6.6%Zn-Al
2O
3 | 8.1 | 6.3 | | |
Embodiment 26 and 27
With the 4.98g particle diameter is that (surface-area is 13m for the particle aluminum fluoride of 0.5-1.4mm
2/ g) add in zinc chloride (II) aqueous solution (0.02g) of 5ml distilled water.This aluminum fluoride is by making aluminum oxide (Harshaw Ltd provides) and hydrogen fluoride in 48 hours in 340 ℃ of reactions.Stirring is to guarantee that solid is by the solution complete wetting.Then by direct heating with this mixture drying, and the solid that obtains sieved, with obtain on aluminum fluoride, containing 0.2%w/w zinc, particle diameter is the final granules of catalyst of 0.5-1.4mm.Except that using zinc chloride (II) solution that increases concentration, repeat above-mentioned steps, to obtain on aluminum fluoride, containing the final catalyzer of 0.5%w/w zinc.
According to the step of embodiment 1-7, under normal atmosphere, get each 2g of these catalyzer and test.
In order to compare, also the activity of the not promoted aluminum fluoride that is used for preparing promoted aluminum fluoride catalyst is tested.Result of study is with 1,1,1, and the percentage yield of 2-Tetrafluoroethane is listed in the table 7.
Table 7
Embodiment | Catalyzer | Temperature of reaction (℃) |
26 27 | 0.2%Zn-AlF
3 0.5%Zn-AlF
3 | 340 | 330 | 320 |
1.8 1.9 | 1.3 1.2 | 0.9 0.9 |
Comparative example | AlF
3 | 0.1 | 0.1 | 0.0 |
Embodiment 28 and 29
In these two embodiment, below the steps outlined catalyzer that utilizes embodiment 7 (embodiment 28) and embodiment 11 (embodiment 29) to make carry out.
The 0.67g catalyzer is filled in the reaction tubes of Inconel(nickel alloys) of 1/4 inch diameter, in 300 ℃ of dryings, and by heating in the flow of hydrogen fluoride of dividing flow velocity at 20ml/ 1 hour and activate, using trieline subsequently is 1: 20 than hydrogen fluoride, be 1 second duration of contact, under atmospheric pressure trieline and hydrogen fluoride added in the reactor.The activity of monitoring catalyst between 210 ℃ and 250 ℃, and the result listed in the table 8 as " original activity ".
Yet, temperature is risen to 350 ℃ of continuous operation 3 days.After this, cool the temperature to 210 ℃-250 ℃, and in the activity of this temperature range monitoring catalyst.Monitoring result is listed in the table 8 as " activity after 3 days ".Then, close trieline and hydrogen fluoride feed, and by heating 2 hours and regenerated catalyst in 350 ℃ in the airflow that divides at 10ml/.Then, divide with 20ml/ respectively and 1ml/ divides and forms hydrogen fluoride again and trieline flows, and in the activity of 210 ℃ of-250 ℃ of monitoring catalysts.Monitoring result is listed in the table 8 as " activity after the regeneration ".All results of study are all with 1-chloro-2,2 in table 8, and the percentage yield of 2-Halothane represents, and show, iron is added in the promoted catalyzer of zinc, and its regeneration is had beneficial effect.
Table 8
Embodiment | Catalyzer | Temperature of reaction (℃) |
28 | 6.6%Zn-Al
2O
3Activity behind the active regeneration of original activity after 3 hours
| 250 | 230 | 210 |
20.1 5.1 5.7 | 13.7 3.3 3.8 | 7.6 1.5 2.0 |
29 | 6%Zn/0.5Fe-Al
2O
3Activity behind the active regeneration of original activity after 3 hours
| 70.2 32.6 74.3 | 48.2 21.1 51.7 | 334 15.4 35.8 |