Method for synthesizing alpha-olefin

Abstract

The invention provides a method for synthesizing alpha-olefin. The method comprises the following steps: carrying out reduction pretreatment on a rare earth element modified iron-based catalyst by adopting hydrogen; wherein the rare earth element comprises one or a combination of more than two of La, Ce and Pr, and the content of the rare earth element is 0.5-3.0 mol%; raw material gas containing hydrogen, carbon monoxide and carbon dioxide is subjected to a synthetic reaction through the pretreated catalyst, and alpha-olefin is obtained, wherein the molar contents of carbon dioxide, hydrogen and carbon monoxide in the feed gas are 2.0-8.0 mol%, 49-86 mol% and 6-49 mol% respectively. According to the method disclosed by the invention, the iron active component in the iron catalyst is regulated and controlled to keep a proper Fe5C2 / Fe3O4 proportion in the reaction operation process, the generation of heavy hydrocarbon and deposition of the heavy hydrocarbon on the surface of the catalyst are reduced, and the activity of the catalyst and the stability of a reaction system are maintained.

Description

Technical Field

[0001] The present invention relates to the technical field of olefin preparation, and in particular to a method for synthesizing alpha-olefin. Background Art

[0002] As an important process for producing α-olefins from non-petroleum resources, the production of α-olefins from synthesis gas has attracted much attention. The most studied route is the production of α-olefins from synthesis gas through Fischer-Tropsch synthesis, but the distribution of product hydrocarbons is affected by the Amderson-Schulz-Flory (ASF) distribution, the carbon number distribution of olefin products is relatively wide, and the selectivity of both low-carbon olefins and high-carbon olefins is low. How to improve the carbon number distribution of Fischer-Tropsch synthesis hydrocarbon products and improve the distribution of target product olefins is the goal of current research on the production of α-olefins from synthesis gas, and catalyst research and development has always been one of the main ways to improve this goal.

[0003] Among the many catalysts studied, iron-based catalysts, as the most studied and cheapest Fischer-Tropsch catalysts, are naturally ideal candidates for the development of synthesis gas to alpha-olefin catalysts. The conversion rate and selectivity of the iron-based catalysts for synthesis gas to alpha-olefins studied recently have been improved. For example, CN109865515A discloses a preparation method for synthesis gas to alpha-olefin catalysts, CN114369002A discloses a two-stage composite catalyst for synthesis gas to alpha-olefins, and CN114369003A discloses a pretreatment method for synthesizing alpha-olefin catalysts, all of which contribute to the improvement of product selectivity in the synthesis gas to alpha-olefin process. However, for the synthesis gas to alpha-olefin reaction system, the stability of the system is still insufficient, and how to improve the stability of the reaction system is still a challenging problem in this research.

[0004] CN114369002A discloses a method for synthesizing linear α-olefins from syngas, comprising the following steps: synthesizing linear α-olefins with a carbon number of 6-15 through a pretreated composite catalyst under the conditions of 200-380°C and 0.5-5.0MPa; wherein the composite catalyst comprises two-stage catalysts, one-stage catalyst is an iron-based catalyst, and the iron-based catalyst has iron oxide and / or iron-containing carbide as active components; the second-stage catalyst is a nickel-based catalyst or a cobalt-based catalyst, and the nickel-based catalyst has nickel oxide as an active component, and the cobalt-based catalyst has cobalt oxide as an active component. CN109865515A discloses a method for preparing a catalyst for preparing linear α-olefins from syngas, and the technology uses one or more alkali metal elements K, Mg, Ca, etc. as electronic additives for the iron catalyst to prepare an efficient syngas conversion catalyst, enhance the carbon chain growth ability, and improve the selectivity of linear α-olefin products. However, the stability of the syngas-to-α-olefin reaction system studied in these two technologies needs to be further improved.

[0005] CN114369003A discloses a pretreatment method for a catalyst for synthesizing α-olefins, which comprises the following steps: sequentially performing the three steps of reduction, carbonylation, and re-reduction, wherein the reduction and re-reduction conditions are the same or different, wherein the reduction and re-reduction refer to the conditions of a reducing atmosphere containing hydrogen, at 250-500°C, 0.01-5.0MPa, and a reducing atmosphere space velocity of 1000-50000ml·h -1 ·gCat -1 The catalyst is reduced under the conditions of 2-30 hours; the carbonylation refers to the carbonylation under the atmosphere containing CO at 250-450°C, 0.01-5.0MPa, and a gas space velocity of 500-50000ml·h -1 ·gCat -1 The carbonylation catalyst is used for 3-50 hours under the conditions of 100 ℃ and 200 ℃. Although the purpose of this technology is to solve the problems of low α-olefin selectivity and poor catalyst stability in the traditional synthesis gas conversion process, the stability of the reaction system studied by this technology still needs to be further improved. Summary of the invention

[0006] To solve the above problems, the object of the present invention is to provide a method for synthesizing α-olefins, which can ensure the stability of the reaction system for synthesizing α-olefins.

[0007] To achieve the above object, the present invention provides a method for synthesizing α-olefins, which comprises the following steps:

[0008] The iron-based catalyst modified by rare earth elements is subjected to reduction pretreatment by using hydrogen; wherein the rare earth elements include one or a combination of two or more of La, Ce, and Pr, and the content of the rare earth elements is 0.5-3.0 mol% based on the total molar amount of the metal elements in the iron-based catalyst;

[0009] A raw gas containing hydrogen, carbon monoxide and carbon dioxide is passed through a pretreated catalyst to perform a synthesis reaction to obtain alpha-olefins; wherein the molar content of carbon dioxide in the raw gas is 2.0-8.0 mol%, the molar content of hydrogen is 49-86 mol%, and the molar content of carbon monoxide is 6-49 mol%.

[0010] In view of the problems of insufficient reaction stability and easy carbon deposition and deactivation of the current iron-based catalyst for synthesizing α-olefins from synthesis gas, the present invention adds an appropriate amount of rare earth metal elements to the iron-based catalyst and controls the appropriate CO2 content in the raw gas to ensure that the iron active components in the iron catalyst are regulated to maintain a suitable Fe5C2 / Fe3O4 ratio during the reaction operation, thereby maintaining the stability of the reaction system.

[0011] The main reason for the deactivation of olefin synthesis catalysts is the carbon accumulation (heavy hydrocarbons) on the catalyst surface. In the synthesis reaction of the present invention, the iron phase of the iron-based catalyst mainly exists in the form of α-Fe, χ-Fe5C2 and Fe3O4. In the initial stage of the synthesis reaction, the α-Fe component formed by high-purity hydrogen reduction activation will react with CO2 and CO in the raw gas to form iron carbide (χ-Fe5C2), and χ-Fe5C2 is the active phase of the synthesis gas and other raw gas to olefin reaction, which can catalyze the Fischer-Tropsch reaction to produce olefins. As the reaction proceeds, the olefins in the reaction atmosphere can in turn promote the formation of iron carbide, inhibit the generation of heavy hydrocarbons, reduce the amount of heavy hydrocarbon carbon accumulation on the catalyst, and prevent the catalyst from deactivating.

[0012] The present invention can maintain the ratio of χ-Fe5C2 / Fe3O4 of active species of the catalyst reaction at a high level by adding rare earth elements such as La, Ce, and Pr to the iron-based catalyst, thereby maintaining the stability of the reaction system. In addition, the addition of rare earth elements can also promote the uniform dispersion of iron elements in the catalyst. At the same time, the present invention also adds CO2 to the raw gas. On the one hand, the combined action of CO2 and high-pressure H2 can promote the generation of active components of iron carbide and inhibit the generation of heavy hydrocarbons; on the other hand, it can effectively reduce the probability of secondary reactions of olefins generated by the reaction. Therefore, the olefin production method provided by the present invention generates less carbon deposits than the prior art within the same reaction time, and the reaction stability of the catalyst is significantly improved.

[0013] According to a specific embodiment of the present invention, preferably, the content of carbon dioxide in the raw gas is 2.0-5.0 mol%.

[0014] According to a specific embodiment of the present invention, preferably, in the raw gas, the molar content of hydrogen is 60-76 mol%, and the molar content of carbon monoxide is 18-32 mol%.

[0015] According to a specific embodiment of the present invention, preferably, in the raw gas, the content of carbon dioxide is 2.0-5.0 mol%, the molar content of hydrogen is 60-76 mol%, and the molar content of carbon monoxide is 18-32 mol%.

[0016] According to a specific embodiment of the present invention, preferably, the volume ratio of hydrogen to carbon monoxide in the raw gas is 2-4.

[0017] According to a specific embodiment of the present invention, preferably, the raw gas is synthesis gas.

[0018] According to a specific embodiment of the present invention, preferably, the temperature of the synthesis reaction is 250-350° C., and the pressure is 1.0-4.0 MPa, preferably 2.0-3.0 MPa.

[0019] According to a specific embodiment of the present invention, preferably, the space velocity of the raw gas is 1000-6000ml·gCat -1 ·h -1 , preferably 2000-5000ml·gCat -1 ·h -1 .

[0020] According to a specific embodiment of the present invention, preferably, the iron-based catalyst modified by rare earth elements contains iron-containing oxides, and the iron-containing oxides include ferrosoferric oxide and / or ferrous oxide.

[0021] According to a specific embodiment of the present invention, preferably, the iron-based catalyst modified by rare earth elements is prepared by a co-precipitation method or an impregnation method.

[0022] According to a specific embodiment of the present invention, preferably, when the co-precipitation method is adopted, the preparation method of the iron-based catalyst modified by the rare earth element is: adding an alkaline solution to a salt solution containing iron elements and rare earth elements to obtain a precipitate, separating the precipitate and drying and calcining it to obtain the iron-based catalyst modified by the rare earth element.

[0023] According to a specific embodiment of the present invention, preferably, when the impregnation method is adopted, the preparation method of the iron-based catalyst modified by the rare earth element is: adding an alkaline solution to a salt solution containing the iron element, separating the precipitate, washing, drying and roasting to obtain the iron-based catalyst, and the iron-based catalyst is impregnated into the salt solution containing the rare earth element. After the impregnation is completed, the solid is taken out and dried and roasted to obtain the iron-based catalyst modified by the rare earth element.

[0024] According to a specific embodiment of the present invention, preferably, in the preparation method of the iron-based catalyst modified by rare earth elements, the calcination temperature is 400-500°C.

[0025] According to a specific embodiment of the present invention, preferably, in the pretreatment of the iron-based catalyst modified by rare earth elements, the reduction reaction temperature is 320-380°C and the reaction time is 4-16h. More preferably, the reduction reaction temperature is 350°C and the reaction time is 8h.

[0026] The technical solution provided by the present invention has the following beneficial effects:

[0027] The present invention adds an appropriate amount of rare earth metal elements to the iron-based catalyst and controls an appropriate CO2 content in the raw gas to ensure that the iron active components in the iron catalyst are regulated to maintain an appropriate Fe5C2 / Fe3O4 ratio during the reaction operation process, reduce the generation of heavy hydrocarbons and their deposition on the catalyst surface, and thus maintain the activity of the catalyst and the stability of the reaction system. BRIEF DESCRIPTION OF THE DRAWINGS

[0028] Figure 1 The Mössbauer spectrum of the catalyst after 500 h of reaction in Example 1;

[0029] Figure 2 This is the Mössbauer spectrum of the catalyst after 500 hours of reaction in Comparative Example 2;

[0030] Figure 3 It is a comparison chart of the reaction stability of the reaction systems of Example 8 and Comparative Examples 1-3. DETAILED DESCRIPTION

[0031] In order to have a clearer understanding of the technical features, purposes and beneficial effects of the present invention, the technical solution of the present invention is now described in detail below, but it should not be construed as limiting the applicable scope of the present invention.

[0032] Example 1

[0033] This embodiment provides a method for synthesizing α-olefins, comprising the following steps:

[0034] (1) Preparation of iron-based catalysts improved by rare earth elements

[0035] 63.78g Fe(NO3)3·9H2O, 94.50g Fe(NO3)2·6H2O and 4.55g La(NO3)3·6H2O were mixed with 500mL water to form an iron salt solution, and 15.30mL of 12.1mol / L HCl solution was added; 500ml of 0.5mol / L K2CO3 solution was added at a uniform rate at 60°C with stirring; within about 2h, the acidic pH value of the solution was adjusted to a pH value of about 9; after the addition was completed, the solution was stirred at a constant temperature for 1h and cooled to room temperature; after the reaction was completed, the deposited product was separated by magnetic field adsorption, washed with deionized water to neutrality, dried, calcined at 450°C, pressed into tablets, and crushed to 20-40 mesh, and the obtained catalyst sample was marked as La-Fe-1-Cat.

[0036] (2) Catalytic reaction

[0037] The catalyst La-Fe-1-Cat obtained in step (1) was filled into a reactor, with a catalyst filling amount of 1 g, and subjected to reduction pretreatment at 350° C. for 8 h under pure hydrogen conditions; after the reduction was completed, the temperature of the reactor was adjusted to 300° C. at a rate of 1° C. / min, and the inlet gas was switched to a reaction raw gas, which was a mixture of H2 / CO / CO2 / N2, with the molar percentages of each gas being H2: 60.6 mol%, CO: 30.3 mol%, CO2: 5 mol%, and N2: 4 mol% (the volume ratio of H2 / CO / CO2 was 2 / 1 / 0.165, with N2 as an internal standard), and the back pressure was set to a reaction pressure of 2.0 MPa. The raw gas was heated to 300° C., 2.0 MPa, and 5000 ml·gCat. -1 ·h -1 The synthesis reaction was carried out under the catalytic conditions of . The catalytic reaction results are shown in Table 1.

[0038] Example 2

[0039] This embodiment provides a method for synthesizing α-olefins, which is the same as that of embodiment 1, except that: in step (1), 4.55 g La(NO3)3·6H2O is replaced by 4.56 g Ce(NO3)6·6H2O, and the obtained catalyst sample is labeled as Ce-Fe-2-Cat; the catalytic conditions in step (2) are replaced by: 320°C, 3.0 MPa, 3000 ml·gCat -1 ·h -1 The catalytic reaction results are shown in Table 1.

[0040] Example 3

[0041] This embodiment provides a method for synthesizing α-olefins, which is the same as that of embodiment 1, except that: in step (1), 4.55 g La(NO3)3·6H2O is replaced by 2.25 g La(NO3)6·6H2O, and the obtained catalyst sample is labeled as La-Fe-3-Cat; the catalytic conditions in step (2) are replaced by: 300°C, 2.0 MPa, 2000 ml·gCat -1 ·h -1 The catalytic reaction results are shown in Table 1.

[0042] Example 4

[0043] This embodiment provides a method for synthesizing α-olefins, which is the same as that of embodiment 1, except that: in step (1), 4.55 g La(NO3)3·6H2O is replaced by 6.55 g La(NO3)6·6H2O, and the obtained catalyst sample is labeled as La-Fe-4-Cat; the catalytic conditions in step (2) are replaced by: 300°C, 3.0 MPa, 2000 ml·gCat -1 ·h -1The catalytic reaction results are shown in Table 1.

[0044] Example 5

[0045] This embodiment provides a method for synthesizing α-olefins, comprising the following steps:

[0046] (1) Preparation of rare earth element-modified iron-based catalysts

[0047] A rare earth element-free iron-based catalyst is prepared, which is labeled as Fe-Cat. The preparation method is the same as step (1) of Example 1, except that La(NO3)3·6H2O is omitted. The obtained catalyst sample without rare earth elements is labeled as Fe-Cat.

[0048] The La element was loaded by the impregnation method: 1.55 g La(NO3)3·6H2O was dissolved in 50 ml water to form a La(NO3)3 solution. Then 25 mL of the formed La(NO3)3 solution was taken and used to impregnate 15 g of the above-mentioned iron-based catalyst Fe-Cat at room temperature for 24 h. The sample was then taken out and dried at 100°C and calcined at 400°C. The obtained catalyst sample was labeled La-Fe-5-Cat.

[0049] (2) Catalytic reaction

[0050] The same as step (2) of Example 1, except that the catalytic conditions were replaced by: 310°C, 2.0 MPa, 4000 ml·gCat -1 ·h -1 The catalytic reaction results are shown in Table 1.

[0051] The evaluation conditions for the catalyst La-Fe-5-Cat prepared in Example 5 were the same as those in Example 1, except that the temperature in the evaluation conditions was replaced by 305°C. A 200-hour reaction stability test of the catalyst was carried out, and the reaction results are listed in Table 1.

[0052] Example 6

[0053] This embodiment provides a method for synthesizing α-olefins, which is the same as that of embodiment 1, except that the catalytic conditions in step (2) are replaced by: 300°C, 2.0 MPa, 2000 ml·gCat -1 ·h -1 The catalytic reaction results are shown in Table 1.

[0054] Example 7

[0055] This embodiment provides a method for synthesizing α-olefins, which is the same as that of embodiment 1, except that the catalytic conditions in step (2) are: 300°C, 2.0 MPa, 2000 ml·gCat -1 ·h -1The molar ratio of each gas in the raw gas (mixed gas of H2 / CO / CO2 / N2) is: H2: 62.66 mol%, CO: 31.33 mol%, CO2: 2 mol%, N2: 4 mol% (volume ratio of H2 / CO / CO2 is 2 / 1 / 0.165). The catalytic reaction results are shown in Table 1.

[0056] Table 1 Catalytic reaction results of Examples 1-7

[0057]

[0058]

[0059] It can be seen from the results in Table 1 that the catalyst prepared in the embodiment of the present invention exhibits excellent α-olefin production reaction performance, and the reaction system can maintain stability.

[0060] Comparative Example 1

[0061] This comparative example provides a method for synthesizing α-olefins, which is the same as Example 1, except that the catalyst used in this comparative example is the catalyst Fe-Cat prepared in Example 5. The catalytic reaction results are shown in Table 2.

[0062] Comparative Example 2

[0063] This comparative example provides a method for synthesizing α-olefins, which is the same as Example 1, except that the catalyst used in this comparative example is the catalyst Fe-Cat (containing no rare earth elements) prepared in Example 5, and the composition of the raw gas is H2: 64 mol%, CO: 32 mol%, N2: 4 mol% (H2 / CO volume ratio is 2 / 1), and does not contain CO2. The catalytic reaction results are shown in Table 2.

[0064] Comparative Example 3

[0065] This comparative example provides a method for synthesizing α-olefins, which is the same as Example 1, except that there is no CO2 in the feed gas in step (2). The catalytic reaction results are shown in Table 2.

[0066] Table 2 Catalytic reaction results of comparative examples 1-3

[0067]

[0068]

[0069] Wherein, α-olefin / olefin (C%) refers to the ratio of α-olefin to the total amount of olefins in terms of carbon number; in Table 2, C 6-15 ＝ is an olefin with a carbon number of 6-15, C 16-18 ＝It is an olefin having a carbon number of 16-18.

[0070] According to Table 1 and Table 2, by comparing the catalytic results of Example 1 with Comparative Examples 1 and 2, it can be seen that the reaction system catalyzed by the iron-based catalyst modified by rare earth elements has higher stability than the unmodified Fe-Cat catalyst. By comparing the catalytic results of Example 1 with Comparative Examples 2 and 3, it can be seen that the raw gas containing an appropriate amount of CO2 can significantly modify the stability of the catalyst and the reaction system compared with the raw gas without CO2.

[0071] Figure 1 and Figure 2 The Mössbauer spectra of the catalysts after 500 h of reaction in Example 1 and Comparative Example 2 are shown respectively. Table 3 and Table 4 are Figure 1 and Figure 2 The corresponding data.

[0072] Table 3 Mössbauer spectroscopy data of the catalyst after 500 h of reaction in Example 1

[0073]

[0074] Table 4 Mössbauer spectroscopy data of the catalyst after 500 h of reaction in Comparative Example 2

[0075]

[0076] From the data results, it can be calculated that the ratio of Fe5C2 / Fe3O4 (in terms of iron element) in the catalyst after 500 hours of reaction in Example 1 is 7.43, and the ratio of Fe5C2 / Fe3O4 (in terms of iron element) in the catalyst after 500 hours of reaction in Comparative Example 2 is 3.65. This proves that the reaction system with appropriate CO2 content in the feed gas and the rare earth element improved catalyst can maintain the Fe5C2 / Fe3O4 ratio of the active species of the catalyst reaction, thereby maintaining the stability of the reaction system.

[0077] In general, the reaction system of the synthesis method of the present invention has excellent reaction stability, which is closely related to the presence of an appropriate amount of CO2 in the raw gas and the rare earth element modification of the catalyst system.

[0078] Example 8

[0079] This example provides a method for synthesizing α-olefins and performs a reaction stability test on the method. The method for synthesizing α-olefins in this example is the same as that in Example 1, except that the catalytic reaction temperature is replaced from 300°C to 305°C. The reaction stability test lasts for 200 hours, and the reaction results are shown in Table 5.

[0080] Table 5 Test results of the stability of the La-Fe-1-Cat catalyst in the synthesis of α-olefins in Example 8

[0081] Reaction time (h) 5 50 100 150 200 CO conversion rate (mol%) 92.8 92.7 92.6 92.4 92.6 Hydrocarbon selectivity (mol%) 60.2 60.4 60.1 60.3 60.0 Olefins / Hydrocarbons (C%) 70.0 70.2 70.1 69.9 70.0 α-Olefin / Olefin (C%) 75.3 75.2 75.1 75.2 75.0

[0082] Figure 3 The reaction stability comparison diagram of the reaction system of Example 8 and Comparative Examples 1-3 is shown. Figure 3 The results show that in the method for synthesizing α-olefins of the present invention, the catalyst maintains good activity and the reaction system also has good stability.

Claims

1. A method for synthesizing α-olefins, comprising the steps of: The iron-based catalyst modified by rare earth elements is subjected to reduction pretreatment using hydrogen; wherein, The rare earth element includes one or a combination of two or more of La, Ce, and Pr, and the content of the rare earth element is 0.5-3.0 mol% based on the total molar amount of the metal elements in the iron-based catalyst; A raw gas containing hydrogen, carbon monoxide and carbon dioxide is passed through a pretreated catalyst to perform a synthesis reaction to obtain alpha-olefins; wherein the molar content of carbon dioxide in the raw gas is 2.0-8.0 mol%, the molar content of hydrogen is 49-86 mol%, and the molar content of carbon monoxide is 6-49 mol%.

2. The method for synthesizing α-olefins according to claim 1, wherein: The rare earth element is La.

3. The method for synthesizing α-olefins according to claim 1, wherein: The content of carbon dioxide in the raw gas is 2.0-5.0 mol%.

4. The method for synthesizing α-olefins according to claim 1, wherein: In the raw gas, the molar content of hydrogen is 60-76 mol%, and the molar content of carbon monoxide is 18-32 mol%.

5. The method for synthesizing α-olefins according to claim 1, wherein: The volume ratio of hydrogen to carbon monoxide in the raw gas is 2-4.

6. The method for synthesizing α-olefins according to any one of claims 1 to 5, wherein: The raw gas is synthesis gas.

7. The method for synthesizing α-olefins according to claim 1, wherein: The temperature of the synthesis reaction is 250-350°C and the pressure is 1.0-4.0MPa.

8. The method for synthesizing α-olefins according to claim 7, wherein: The pressure of the synthesis reaction is 2.0-3.0MPa.

9. The method for synthesizing α-olefins according to claim 1, wherein: The space velocity of the raw gas is 1000-6000ml·gCat -1 ·h -1 .

10. The method for synthesizing α-olefins according to claim 9, wherein: The space velocity of the raw gas is 2000-5000ml·gCat -1 ·h -1 .

11. The method for synthesizing α-olefins according to claim 1, wherein: The iron-based catalyst modified by rare earth elements contains iron-containing oxides, and the iron-containing oxides include ferrosoferric oxide and / or ferrous oxide.

12. The method for synthesizing α-olefins according to claim 1, wherein: The iron-based catalyst modified by rare earth elements is prepared by co-precipitation or impregnation.

13. The method for synthesizing α-olefins according to claim 12, wherein: When the co-precipitation method is adopted, the preparation method of the iron-based catalyst modified by rare earth elements is: adding an alkaline solution to a salt solution containing iron elements and rare earth elements to obtain a precipitate, separating the precipitate, washing, drying and roasting to obtain the iron-based catalyst modified by rare earth elements.

14. The method for synthesizing α-olefins according to claim 12, wherein: When the impregnation method is adopted, the preparation method of the iron-based catalyst modified by rare earth elements is as follows: an alkaline solution is added dropwise to a salt solution containing iron elements, a precipitate is separated, and an iron-based catalyst is obtained through washing, drying and roasting. The iron-based catalyst is impregnated into a salt solution containing rare earth elements, and after the impregnation is completed, the solid is taken out and dried and roasted to obtain the iron-based catalyst modified by rare earth elements.

15. The method for synthesizing α-olefins according to claim 13 or 14, wherein: The calcination temperature is 400-500℃.

16. The method for synthesizing α-olefins according to claim 1, wherein: In the pretreatment of the iron-based catalyst modified by rare earth elements, the reduction reaction temperature is 320-380° C. and the reaction time is 4-16 hours.

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