• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
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  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    Unsaturated gasolines of both high mercaptan or hydrogen sulfide content and high gum-generator content are hydrogenated first over a palladium catalyst and then over a nickel catalyst. Resultant unsaturated gasolines are sweet and have low gum-generator content.
    公开号:SU886752A3
    申请号:SU782690453
    申请日:1978-11-29
    公开日:1981-11-30
    发明作者:Козин Жан；Деррьен Мишель
    申请人:Энститю Франсэ Дю Петроль (Фирма)；
    IPC主号:
    专利说明:

    (S) METHOD FOR SELECTIVE HYDROGENATION OF PETROL
    I
    The invention relates to a method for the selective hydrogenation of gasoline containing both mono-olefins, resin-forming compounds and undesirable sulfur compounds, in particular g mercaptans and / or hydrogen sulfide, and can be used in the petrochemical industry.
    As a result of pyrolysis or cracking processes, especially steam cracking, such hydrocarbons as gasolines or light distillate fractions, olefins, in particular ethylene, and gasolines are formed. The gasolines thus obtained are unstable due to the presence of gum-forming substances in them.
    The use of gas oil fractions as a raw material leads to an increase in the content of sulfur compounds 20 and resin-forming compounds, such as diolefins, styrene compounds, etc.
    Methods are known for the selective hydrogenation of gasolines containing one to five.
    temporarily monoolefins, resin-forming compounds and sulfur compounds by contacting the feedstock in the presence of hydrogen with a catalyst containing palladium. The product obtained is subjected to hydrotreatment at 350–380 ° C in the presence of aluminum-molybdenum or other catalysts to completely hydrogenate unsaturated hydrocarbons and reduce sulfur compounds. The process is usually carried out in a single stream with intermediate heating of the raw material 1.
    Closest to the proposed method is the selective hydrogenation of gasoline containing mono-olefins, resin-forming compounds and at least 10 ppm of mercaptans and / or giving a positive result in the experience with sodium plumbite by contacting the feedstock in the presence of hydrogen at 30-250 ° C with a catalyst containing 0% by weight of palladium on alumina. The product obtained is then subjected to hydrotreatment in the presence of hydrodesulfurization catalysts. Hydroprocessing is carried out at 177 311s in the presence of a desulfurizing catalyst G2. However, mono-olefins are also subjected to hydrogenation. Thus, the target product does not satisfy the requirements applied to motor fuel. The purpose of the invention is to improve the quality of the target product. The goal is achieved by the described method of selective hydrogenation of gasoline containing monoolefins, resin-forming compounds and at least 10 ppm of mercaptans and / or giving a positive result in the experience with plumbito sodium by contacting the feedstock in the presence of hydrogen with a catalyst containing 0, weight, palladium on alumina, followed by hydrotreatment of the obtained product in the presence of a catalyst. containing 2–50 wt.% nickel on oxide carrier at 30–250 ° C with the process of selective hydrogenation with the volume of the catalyst containing palladium and the volume of the catalyst containing nickel constituting 10 80 and 20–90%, respectively, of the total volume of catalysts . Distinctive features of the method include conducting a hydrotreatment in the presence of a catalyst containing 2-50 wtC nickel on an oxide carrier at 30-250 ° C and carrying out a process of selective hydrogenation with a volume of catalyst containing palladium and 10% of catalysts containing nickel. -80% and 20-90%, respectively, of the total volume of the catalyst. The proposed method is carried out under the following conditions: temperature 30250 ° C, preferably 50-200 0-, total pressure 10-100 bar, preferably 20-50 barJ spatial velocity or the ratio of the volume of liquid loading (gasolines) to catalyst volume per hour 0, 5-10, preferably 2-5 molar ratio of hydrogen / charge (gasoline 0.1-2, preferably 0.5-1.5. It is advisable to use fixed beds of catalysts, which can be located one after the other or one above the other in the same and 2 same reactors, or in two or more different reactors The preferred carriers in the catalysts are neutral carriers, i.e., those with low or no acidity. Acidity can be measured, for example, using an ammonia absorption test 3. The acidity of the carriers used at various stages of the process, can be measured in the heat of absorption of ammonia on the carrier at a pressure of 10 mm pToSt. The heat of absorption is determined by the formula: Heat released (expressed in .. calories x per gram of carrier) - Amount of ammonia absorbed (expressed in mmol X NHj per gram of carrier) These two measurements are carried out using a microgravitometer and thermal differential analysis at the temperature at which the catalyst will be used. The carrier is considered to be substantially neutral when the dN value is below 0.0, weakly acidic, when the lN value is between 0.0 and 0.1. As carriers it is possible to use compounds of metals of 11,111 and IV groups of the periodic system of elements, for example silicates or. oxides of these metals, preferably alumina, in particular alumina with a specific surface of 30-150 MVr, preferably 50-100 m / Go Preferably, the volume of the catalyst containing palladium is, and the volume of the catalyst containing nickel is 60-85% of the total catalyst. The desired content of palladium in the catalyst is 0.1-0.5% by weight and nickel, 0% by weight. Example 1 (comparative) o The raw material used is gasoline obtained by gas oil steam cracking and having the following characteristics: Method Results Bulk mass at 15 ° СNFT 60-1П10.859 ASTM distillation, ° СNFM 07-002 boiling point 55 50 % boils at 111 boiling point Total sulfur, weight. Cho on mil NFM 07-0 1500 Sulfur, weight.h, for milMercaptan sulfur, weight.h. NFM 07-031 per million Corrosion of copper 07-015 stripsNF Experience with plumpy positive sodium (Ph.D. telprob) NFM 07-0.05 Bromine number, g Vg / 100 g NFM 07-017 Malein number, mg maleino, total anhydride / g gasolineNOP 326-58 Induction period from 20 weight.h. on antioxidant and lion (M, M-divtorbutylparaphenylenediamine, NFM 07-012 20 Octane number (with 0.05 tetraethylNFM 07-026 98 lead) Source gasoline mixed with hydrogen is passed through a reactor filled with a catalyst consisting of 0 , 3 weight, palladium, deposited from palladium nitrate on a carrier of alumina with a specific surface 70. The acidity of alumina in the test described above is 0.03 after treatment of ammonia of ammonia. Before use, the catalyst is calcined for 2 hours. , then reduced with hydrogen at 100 ° C for 2 times. The process conditions are as follows: Spatial speed, volume (volume / hj Average temperature, ° C Total pressure, bar HQ / load ratio, mol 886752, ra (13) a sample of 100. 4 The product obtained after the limited partnership has the following main indicators: Bromine number, G Br / 100 g Malein number, mg maleic anhydride / g product Induction period with 20 million shares of antioxidant, min Mercaptan sulfur, weight.h, per million Total sulfur, weight, h per million Corrosion of copper strip Experience with plumbing Put it in ny Octane (0.05 tetraethyl paddles 98 thus allows katazator used pseudo-full progidrovat smoloobrazuyuschie aleinovoe compound number 2), but does not contain the mercaptans is reduced - even much increased. So fram, the resulting gasoline can not be used as a top car. After 1000 hours of conducting the process, the recovered product possesses the same attribute. PRI me R 2 (comparative). The gasoline used in Prize 1 is hydrogenated. Hydrogenation is carried out in a reactor filled with a catalyst consisting of 10 ppm nickel deposited from nickel nitrate on a carrier identical to that of Example 1, which is potassium hydrated for 2 hours at which time it is reduced by hydrogen The working conditions for priu are used 1. The product obtained after working hours has the following characteristics: Bromine number g Vg / 100 g "3 Malein number, mg of maleic anhydride / g product 10 Induction period from 20 weight parts. per million of antioxidant, min. Mercaptan sulfur, parts by weight per million6 Total sulfur, parts by weight per million1500 Corrosion of copper plate1a Experience with no plumbbit- Negative Octane number (from 0.05 wtD) of tetraethyl lead 98 From the data it can be seen that the degree of hydrogenation of resin-forming products is significantly less than in Example 1, so gasoline used as fuels must have a malein number below 5. The value of the indicator mercaptan sulfur meets the requirements for motor fuel. After 1000 hours of testing, the maleic anhydride value of the hydrogenated product is 15. Thus, catalyst deactivation occurs over time. PRI me R 3 (according to the invention). Use the raw materials of example 1. Raw materials are passed in the presence of hydrogen through a reactor containing two layers of catalyst. The first layer occupies 1/3 of the total volume and is the reduced palladium catalyst of Example 1, and the Bromine number is g Br / 100 g i2 Maleic number, mg maleic anhydride / g product Induction period with 20 weight parts. per million of antioxidant, min. Mercaptan sulfur, parts by weight per million Total sulfur, parts by weight per million Corrosion of copper plate Experience with sodium plumbbit Octane number (0.05 wt. of tetraethyl lead) 98 3,5 500 7 1490 la Negative 28 second, occupying 2/3 volume, represents the reduced nickel catalyst of example 2. Condition the same as in examples 1 and 2, the results of the experiment are shown in table 1, example k (comparative. Repeat example 3, located in the reactor first nickel catalyst (1/3 of the total volume, then palladium catalyst (2/3 of the total volume The composition of the catalysts and the process conditions are not changed. The results of the experiment p and shown in Table 1. Example 5 (according to the invention). Example 3 was repeated, modifying the relative proportions of the catalysts: 15% by volume of palladium catalyst, then 85% by volume of the nickel catalyst. Other conditions were not changed. 6 (according to the invention. Example 3 is repeated, modifying the relative proportions of the catalysts: 50% by volume of palladium catalyst, then 50% by volume of nickel catalyst .. Other conditions are not changed. In tab. 1 shows the characteristics of the products obtained after 100 hours of testing. Table 1 41 2.5 “, 8 2.7 480 530 20 i 9 15001i 901500 la la la Put-Negate-Negative body 9B 98 98 Thus, the products obtained in examples 3, 5 and 6 satisfy the maleic number , m Kaptan sulfur and experience with plumbing. After 1000 hours of testing, the hydrogenated product of Example 3 satisfies the requirements: maleic number, 5 experience with plumbit is negative, me- naphthan sulfur, 8 parts by weight. in a million. Examples 7-10. The raw material used is gasoline obtained by cracking with naphtha vapor, which has the following characteristics: Bulk weight at 15 ° С 0.830 Distillation А5ТМ, С 55-199 Total sulfur, weight, per million Mercaptan sulfur, weight.h. per million Sulfur dissolved, weight. hours per million maleic number, mg maleic anhydride / g of product
    Note. () - positive experience;
    (-) - negative experience.
    From the comparative data it follows that the use of the catalysts of examples 8-10 gives acceptable results only after 50 hours of operation, then a strong deactivation of the catalysts of examples 8 and 10 is observed. The catalyst of example 9 is stable.
    权利要求:
    Claims (1)
    [1]
    Invention Formula
    A method of selectively hydrogenating gasoline containing mono-olefins, resin-forming compounds and at least 10 hours per million mercaptans and / or giving a positive result in the experience with sodium plumbite by contacting the feedstock in the presence of hydrogen at 30-25 ° C with a catalyst containing 0.05 -5.00 ppm of palladium on an oxide carrier followed by hydrotreating the product obtained in the presence of a catalyst at an elevated temperature, distinguished by the fact that, in order to increase the quality2 Bromine number g / V g 100 g Putting plumbit sodium. Experiments were carried out under the following conditions: temperature, total pressure 30 bar, space velocity 2 volume / volume / h, molar ratio H2 / benzine 0.5. The following catalysts are used: example 7 (comparative - catalyst of example 1; example 8 (comparative catalyst of example 2; example 9 (according to the invention - 25 vol. of the palladium catalyst of example 1 and 75 o6.S nickel catalyst of example 2; example 10 (comparative - 75 vol.% nickel catalyst of example 2 and 25 vol.% palladium catalyst example 1. in tab. 2 shows the characteristics of the products after 50 hours and 1000 hours of testing. I Table2
    11 88675212
    properties of the target product, hydrotreating-1, Composition and methods of processing are carried out in the presence of liquid catalysts of pyrolysis. A theme containing 2-50% nickel per capita reviews. Ser, Neftekhimi and slanoxide carrier at 30–250 ° С and pro cessing, M., TsNIITEneftekhim, process of selective hydrogenation of Pro-j 19b9, p. . d t when the volume of the catalyst containing palladium and the volume of the catalyst, lp1197e containing nickel, are 2- USSR N ° 4042/3, 10-80% and 20-90% of, respectively, of cl. C 10 G 23/0, 1968 (prototype). the total amount of catalysts.
    Sources of information, 3. Journal of Catalysis, 1963,
    taken into account in examination2, p. 211-222.
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    同族专利:
    公开号 | 公开日
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    IT7830259D0|1978-11-28|
    FR2410038A1|1979-06-22|
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    引用文献:
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    DE1545323A1|1964-06-19|1969-11-27|Lummus Co|Process for the hydrogen treatment of a gasoline pyrolysis fraction|
    US3470085A|1967-11-20|1969-09-30|Universal Oil Prod Co|Method for stabilizing pyrolysis gasoline|
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    US3846278A|1971-09-02|1974-11-05|Lummus Co|Production of jet fuel|DE3127751A1|1981-07-14|1983-02-03|EC Erdölchemie GmbH, 5000 Köln|METHOD FOR HYDROGENATING HYDROCARBONS|
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR7736221A|FR2410038B1|1977-11-29|1977-11-29|
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