Selective hydrogenation catalyst for pyrolysis gasoline

Catalyst – solid sorbent – or support therefor: product or process – Catalyst or precursor therefor – Metal – metal oxide or metal hydroxide

Reexamination Certificate

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Details

C502S327000, C502S329000, C502S330000, C502S331000, C502S332000, C502S333000, C502S339000

Reexamination Certificate

active

06576586

ABSTRACT:

This invention involves a selective hydrogenation catalyst for pyrolysis gasoline and the preparation thereof.
THE BACKGROUND OF THE INVENTION
At present, the selective hydrogenation catalyst for industrial pyrolysis gasoline is still taking palladium-based catalyst as the main. There is also the palladium catalyst added with the catalyst promoter. Most of the co-activating component is elements of IA group in the periodical table of elements. For those materials of pyrolysis gasoline with high impurity, the noble metal nickel catalyst has been used for a long time. Because of its slow starting temperature, high hydrogenation activation, large precession material quantity and long lifetime etc, the palladium-based catalyst is obviously superior to catalyst of nickel group, for example, as disclosed in U.S. Pat. No. 4,410,455. But when pyrolysis gasoline contains high diene and the impurities such as arsenic and colloid, many of the industrialized palladium-based catalysts are difficult to operation with stability and for a long time in designed space velocity. It frequently occurs that even though the designed space velocity of catalyst can reach 4.7 h
−1
during the procedure of fresh feed-in, but it only can operate with a reduced space velocity of 2.8 h
−1
due to too heavy feed-in and too much impurity.
In order to overcome the deficiency of the prior arts, the object of the present invention is to provide a series of palladium-based hydrogenation catalysts that are adaptive for raw material with high impurity and suitable for operation under high space velocity. Another object of the present invention is to provide a preparation method of a series of palladium-based hydrogenation catalysts.
THE SUMMARY OF THE INVENTION
According to the present invention, a selective hydrogenation catalyst for pyrolysis gasoline is provided, wherein the catalyst mainly consists of a support of &dgr;, &agr; mixed alumina covered by palladium as active component and alkali metal and/or alkaline-earth metal. The palladium is distributed like egg shell on the support surface. And said support has 0.5-0.9 ml/g of specific pore volume, wherein 40-200 Å pores account for more than 85% of the total pore volume, preferably, 100-200 Å pore volume accounts for 65%-80% of the said total pore volume in catalyst support. The specific surface area is about 70-140 m
2
/g. And &agr; crystal type in the alumina support is about 0.1~5% based on the weight percentage of &dgr;, &agr; mixed alumina support. Said catalyst comprises palladium in amount of 0.05-0.4 wt %, alkali metal and/or alkaline-earth metal in amount of 0.05-2.0 wt %.
The present invention is also related to a selective hydrogenation catalyst for pyrolysis gasoline, wherein the catalyst mainly consists of a support of &dgr;, &agr; mixed alumina covered by palladium as active component, promoter as co-active component and alkali metal and/or alkaline-earth metal. Said palladium is distributed like egg shell on the support surface. Said support has 0.5-0.9 ml/g of specific pore volume, wherein 40-200 Å pores account for more than 85% of the total pore volume, preferably 100-200 Å pore volume accounts for 65%-80% of the said total pore volume in catalyst support. The specific surface area is about 70-140 m
2
/g, and a crystal type in the alumina support is about 0.1-5% based on the weight percentage of &dgr;, &agr; mixed alumina support, said catalyst containing promoter having selected one from a group of the VIB or IB elements in the periodical table of elements. The ratio of promoter and palladium by weight is about 0.2-2:1. The alkali metal and/or alkaline-earth metal is added in amount of 0.05-2.0 wt %.
According to the invention, the shape of the said catalyst can be either of mechanical punching or of clover or cylinder bar. The shape of support grain does not influence the application of this invention.
The present catalyst is adaptive for hydrogenation of total fraction of pyrolysis “gasoline and C
6
-C
8
intermediate fraction petrol.
The preparation method of catalyst of this invention is used by the method that is known to the person skilled in the arts. In general, that is to say it is the same to the immersion technology for making ordinary lamella catalyst. Therefore, the present invention is to provide a method for preparation of a selective hydrogenation catalyst for pyrolysis gasoline comprising the following steps:
(i) preparing aqueous solution containing palladium and alkali metal and/or alkaline-earth metal in amount of 0.05-2.0 wt %, the pH of said solution being less than 4;
(ii) immersing &dgr;, &agr; mixed Al
2
O
3
support in said solution at 100-150° C.;
(iii) sintering the immersed support at about 380-500° C. to get a catalyst.
In the method of the invention, a promoter is applied to form immersion solution. Said promoter is selected from a group of the VIB or IB elements in the periodical table of elements.
In addition, ratio of promoter and palladium by weight in the present method is defined to 0.2-2:1.
In another words, Firstly, solution which can be mutual-soluble with the immersion liquid (for example the deionized water) is used to immerse the pre-immersed support, then the pre-immersed &dgr;, &agr; mixed alumina support is immersed with salt solution having active component such as palladium. After washing, drying and sintering, the immersed support will become a final product of oxide-type catalyst. The catalyst product can be used after the deoxidization by putting in hydrogen in reactor.
The promoter in the invention can form a complex with palladium. The formation of such a complex is beneficial to the even distribution of palladium grains, and to improve and increase the utilization factor of palladium, and to reduce the loss of palladium and extend the lifetime of catalyst. The alkali metals can change the acid-base status of support surface, which is beneficial to reduce sedimentation of colloid and carbon in hydrogenation period. The pores are evenly distributed, which has the function of reducing the inner diffusion resistance. The larger specific pore volume is beneficial to the material with a bigger procession quantity and higher impurity contents. In combination of the above-mentioned factors, the catalyst of this invention is especially adaptive for the procession of material with high impurity contents as well as for the hydrogenation under higher space velocity. For example, the procession of total fraction pyrolysis gasoline of colloid will be <60 mg/100 ml, diene value <40 g iodin/100 g petrol, especially under the space velocity of 4.0-6.0 h
−1
(fresh oil), it can carry out the hydrogenation to the C
6
-C
8
medium petrol.
The catalyst can be prepared classically by the shell layer immersion technology as known by the skilled in the arts. During the preparation, the elements as promoter selected from a group of the VIB, IB, IA and IIA in the Periodical Table of Elements are applied. Their oxides, hydroxides and organic and inorganic salts of the promoter elements are preferable to be used in the present invention. These substances are added to fully dissolve to make immersion solution. In addition, said support may be pre-immersed with solution that can mix with immersion solution each other.
The advantages of this invention are that the large quantity of materials can be treated (for C
6
-C
8
medium fraction petrol, the space velocity can reach 4.0-6.0h
−1
when the fresh petrol is calculated); for the treatment of material with high impurities, the hydrogenation activity is high with good selectivity. The chemical stability and the thermal stability are much better during the long period operation. The sol performance is good and the carbon quantity is low. The catalyst has long lifetime and the preparation thereof is simple.
The foregoing and other advantages of the invention will appear from the following description. These embodiments do not represent the full scope of the invention. Thus, the claim should be looked to in order to

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