Fused-ring alkane fuel and photocatalytic preparation process thereof

Info

Publication number: 20200181040
Type: Application
Filed: Jul 9, 2018
Publication Date: Jun 11, 2020
Applicant: TIANJIN UNIVERSITY (Tianjin)
Inventors: Jijun ZOU (Tianjin), Lun PAN (Tianjin), Xiangwen ZHANG (Tianjin), Qingfa WANG (Tianjin)
Application Number: 16/498,386

Abstract

A process for preparing a fused-ring alkane fuel, wherein the fused-ring alkane fuel has the following structure: wherein n is 1 or 2; R1, R2, R3, R4 and R5 are H or —CH3 or —CH2CH3; the fused-ring alkane fuel has a density of greater than 0.870 g/cm3, a freezing point of not higher than −50° C., and a net mass heat value of not less than 42.0 MJ/kg; the process for preparing a fused-ring alkane fuel, wherein the process includes steps of: (1) in a presence of ultraviolet light and a photocatalyst, a Diels-Alder cycloaddition reaction between a substituted or unsubstituted cyclic enone and a substituted or unsubstituted furan molecule occurs to produce a fuel precursor molecule: (2) the fuel precursor molecule obtained in the step (1) is subjected to hydrodeoxygenation to produce the fused-ring alkane fuel.

Description

Description

CROSS REFERENCE TO THE RELATED APPLICATIONS

This application is the national phase entry of International Application No. PCT/CN2018/095036, filed on Jul. 9, 2018, which is based upon and claims priority to Chinese Patent Application No. 2018107445428, filed on Jul. 9, 2018, the entire contents of which are incorporated herein by reference.

TECHNICAL FIELD

The invention is in the technical field of liquid fuel propellant, and particularly, it relates to a high density liquid fuels of fused-ring alkane and a preparation process thereof via a photocatalytic Diels-Alder cycloaddition reaction.

BACKGROUND

High density hydrocarbon fuel is an important component of liquid propellants for aircrafts, being a key for providing power guarantee for aircrafts such as airplanes, missiles and rockets, and thus, the quality of the fuel will decide the flight performances (including flying range, flying speed, and effective loads) of the aircrafts. For an aerospace aircraft having a definitive volume, the higher the density of the liquid fuel is, the higher the mass of the fuel carried by the aircraft is; the higher the volumetric heat value of the fuel, the higher the energy released by consuming per unit volume of the fuel. These characteristics of the fuel will be more beneficial to the performances of the aircrafts in various aspects. Alternatively, on the premise of keeping the performances of aircrafts unchanged, using a high density fuel can reduce the volume of used oil tanks, minimize the volume of the aircrafts, and increase the penetration ability and mobility of the aircrafts.

Fused-ring alkane fuel is a kind of liquid fuel having high density, high heat value, low freezing point and high thermal stability. For example, decalin has a molecular density of 0.88 g/mL, a freezing point of less than −30° C., and a net combustion heat value of more than 37.4 MJ/L, and it is excellent in thermal stability. Thus, this material is a main component of high density thermally stable jet fuels (e.g., JP-900). There are many reports regarding processes of preparing the fused-cycle alkane fuel molecules. In the document “Sustainable Chemistry & Engineering, 2016, 4, 6160” in the document ACS reports, by taking cyclopentanol as a raw material, the cyclopentanol is catalytically dehydrated to produce cyclopentene, then the cyclopentene takes an intermolecular alkylation reaction to produce a fuel precursor such as decalin, and at last, the fuel precursor is hydrogenated under high pressure to produce a mixture of decalin (77 wt %) and C₁₅alkanes, the mixture having a density of 0.90 g/mL. In the document “Chemical Engineering Science, 2018, 180, 64”, concentrated sulfuric acid is utilized to catalyze the one-pot reaction of a cyclic alcohol and a branched cycloalkane to perform continuous dehydration, alkylation, rearrangement and hydrogen transfer, thereby to obtain branched naphthalene alkanes having a density of 0.88 g/mL or above and a freezing point as low as −110° C. However, these processes have complicated procedures and complex operations, or they will produce strong corrosions to associated apparatus, or they have a low selectivity to fused-ring alkane products. Thus, it is a challenge to produce fused-ring multi-ring alkane fuel with high selectivity under mild conditions.

SUMMARY

The object of the invention is to provide a high density fuel molecule of substituted fused-ring alkane that is prepared by using a photocatalytic process. The process has the advantages of mild process conditions, high substrate universality, and high selectivity to target product.

A first aspect of the invention relates to a fused-ring alkane fuel characterized in that the fuel has the following structure:

wherein n is 1 or 2; R₁, R₂, R₃, R₄and R₅are H or —CH₃or —CH₂CH₃.

Preferably, the fuel has a density of greater than 0.870 g/cm³, a freezing point of not higher than −50° C., and a net mass heat value of not less than 42.0 MJ/kg.

A second aspect of the invention discloses a process for the preparation of the fused-ring alkane fuel, characterized in that the process includes the steps of:

(1) In the presence of ultraviolet light and a photocatalyst, a Diels-Alder cycloaddition reaction between a substituted or unsubstituted cycloenone and a substituted or unsubstituted furan molecule occurs to produce a fuel precursor molecule:

(2) Under certain conditions, the fuel precursor molecule obtained in the step (1) is subjected to hydrodeoxygenation to produce the fused-ring alkane fuel:

Preferably, the photocatalyst in the step (1) is one or more selected from the group of ZnO/HZSM-5, ZnO/Na-ZSM, ZnO/Hβ, ZnO/HY, ZnO/LaY, Ti-MCM-41, TiO₂/Al₂O₃, TiO₂/SiO₂, TiO₂/MK-10, TiO₂/SBA-15, P25, ZnO/C₃N₄, TiO₂/C₃N₄, ZnO/WO₃, TiO₂/WO₃, C₃N₄, WO₃, WO_2.72. The photocatalyst is added in an amount of 1 to 20% by weight of the reactants; the reaction temperature ranges from −40° C. and 30° C., and the reaction time ranges from 9 h to 24 h.

Preferably, the substituted or unsubstituted cycloenones as described in the step (1) is one or more selected from the group of cyclopentenone, 3-methyl-2-cyclopentenone, 4-methyl-2-cyclopentenone, 5-methyl-2-cyclopentenone, 4,4′-dimethyl-2-cyclopentenone, 3,4-dimethyl-2-cyclopentenone, 3,5-dimethyl-2-cyclopentenone, 4,5-dimethyl-2-cyclopentenone, 3,4,4′-trimethyl-2-cyclopentenone, 3,4,5-trimethyl-2-cyclopentenone, 3-ethyl-2-cyclopentenone, 4-ethyl-2-cyclopentenone, 5-ethyl-2-cyclopentenone, 4,4′-diethyl-2-cyclopentenone, 3,4-diethyl-2-cyclopentenone, 3,5-diethyl-2-cyclopentenone, 4,5-diethyl-2-cyclopentenone, 3,4,4′-triethyl-2-cyclopentenone, 3,4,5-triethyl-2-cyclopentenone, cyclohexenone, 2-methyl-2-cyclohexenone, 3-methyl-2-cyclohexenone, 4-methyl-2-cyclohexenone, 5-methyl-2-cyclohexenone, 6-methyl-2-cyclohexenone, 2,3-dimethyl-2-cyclohexenone, 2,4-dimethyl-2-cyclohexenone, 2,5-dimethyl-2-cyclohexenone, 2,6-dimethyl-2-cyclohexenone, 3,4-dimethyl-2-cyclohexenone, 3,5-dimethyl-2-cyclohexenone, 3,6-dimethyl-2-cyclohexenone, 4,5-dimethyl-2-cyclohexenone, 4,6-dimethyl-2-cyclohexenone, 5,6-dimethyl-2-cyclohexenone, 2-ethyl-2-cyclohexenone, 3-ethyl-2-cyclohexenone, 4-ethyl-2-cyclohexenone, 5-ethyl-2-cyclohexenone, 6-ethyl-2-cyclohexenone, 2,3-diethyl-2-cyclohexenone, 2,4-diethyl-2-cyclohexenone, 2,5-diethyl-2-cyclohexenone, 2,6-diethyl-2-cyclohexenone, 3,4-diethyl-2-cyclohexenone, 3,5-diethyl-2-cyclohexenone, 3,6-diethyl-2-cyclohexenone, 4,5-diethyl-2-cyclohexenone, 4,6-diethyl-2-cyclohexenone, 5,6-diethyl-2-cyclohexenone, 2,3,4-trimethyl-2-cyclohexenone, 2,3,5-trimethyl-2-cyclohexenone, 2,3,6-trimethyl-2-cyclohexenone, 3,4,5-trimethyl-2-cyclohexenone, 3,4,6-trimethyl-2-cyclohexenone and 4,5,6-trimethyl-2-cyclohexenone.

The substituted or unsubstituted furan is one or more selected from the group of furan, 2-methylfuran, 3-methylfuran, 2,3-dimethylfuran, 2,4-dimethylfuran, 2,5-dimethylfuran, 2-ethylfuran, 3-ethylfuran, 2,3-diethylfuran, 2,4-diethylfuran and 2,5-diethylfuran.

The substituted or unsubstituted cycloenones is not higher than 40 wt % based on the total mass of the substituted or unsubstituted cycloenones and the substituted or unsubstituted furan.

Preferably, the fuel precursor molecule in the step (2) is hydrodeoxygenated under the following conditions: in the presence of a hydrodeoxygenation catalyst, a reaction temperature of 200° C. to 280° C., a hydrogen gas pressure of 4 MPa to 8 MPa, and a reaction time of 24 h to 48 h.

Preferably, the hydrodeoxygenation catalyst is one or more of copper, nickel, platinum, gold or palladium loaded on one or more of supporters Al₂O₃, SiO₂, HZ SM-5, MCM-41, Hβ, SBA-15 or HY. The hydrodeoxygenation catalyst is added in an amount of 1 to 40% by weight of the fuel precursor molecule.

Preferably, the ultraviolet light in the step (1) is light having a wavelength between 300 nm and 360 nm.

A third aspect of the invention discloses the use of the photocatalyst in step (1) for increasing the selectivity to the target product of a cycloaddition reaction between a substituted or unsubstituted cycloenones and a substituted or unsubstituted furan molecule.

The invention has the following advantages.

1. The fused-ring alkane fuels of the invention have excellent performances of high density, high heat value, low freezing point, and high thermal stability, and particularly, the density that is far higher than that of traditional aviation kerosene (the density is generally 0.78 g/mL). For aerospace crafts with limited volume of oil tanks, the fuels can effectively increase oil carrying quality and satisfy application requirements in long flying range, high flying speed, and large load.

2. After adding a photocatalyst to the Diels-Alder cycloaddition reaction of the invention, the selectivity to the target product of the photocatalytic reaction (i.e., the [2+4] cycloaddition reaction between substituted or unsubstituted cycloenones and substituted or unsubstituted furan molecules) is greatly increased, while the photochemical [2+2] products of the substituted or unsubstituted cycloenones per se and the photochemical [2+2] products of the reaction between the substituted or unsubstituted cycloenones and the substituted or unsubstituted furansare greatly reduced (see Examples 1 and 2 of the invention). Thereby, the quality of the fused-ring alkane fuels of the invention is greatly improved.

3. The photocatalytic process for preparation of the fused-ring alkane fuels of the invention may be performed via a Diels-Alder reaction of heterogeneous system and a hydrodeoxygenation reaction at normal temperature and at normal pressure, and the process has the advantages of mild process conditions, high substrate universality and high selectivity to target products. Thus, the process has a great value in industrial application.

DETAILED DESCRIPTION OF THE EMBODIMENTS

The invention is further illustrated by combining the following examples, and the examples are only illustrative but not limited. Table 1 shows the synthesis reaction of the fuel precursor molecules in Examples 1-30.

TABLE 1 Fuel Precursor molecule Synthesis Reactions Catalyst Yield of Raw amount fuel Serial Raw materials material (in reactant)/ Reaction Reaction precursor No. (mass ratio) mass/g Catalyst wt % temperature/° C. time/h molecules/% Example 1 30% 20 None 10 10 24 30 cyclopentenone 70% furan Example 2 30% 20 ZnO/HZSM-5 10 10 24 90 cyclopentenone 70% furan Example 3 30% of4,4′- 20 ZnO/HZSM-5 5 30 24 80 dimethyl-2- cyclopentenone 70% furan Example 4 20% of 3,4,5- 20 ZnO/HZSM-5 20 30 24 89 trimethyl-2- cyclopentenone 80% furan Example 5 40% 20 ZnO/HY 1 −40 20 66 cyclohexenone 60% furan Example 6 30% 2-methyl-2- 20 ZnO/HY 10 10 24 83 cyclohexenone 70% furan Example 7 20% 3,5- 20 ZnO/LaY 10 10 24 82 dimethyl-2- cyclohexenone 80% furan Example 8 10% 2,3,5 - 20 ZnO/LaY 10 25 24 78 trimethyl-2- cyclohexenone 90% furan Example 9 20% of 3-ethyl-2- 20 Ti-MCM-41 10 30 24 86 cyclopentenone 80% furan Example 10 30% of 3-ethyl-2- 20 Ti-MCM-41 20 0 24 88 cyclohexenone 70% 2- methylfuran Example 11 30% of 3-ethyl-2- 20 Ti-MCM-41 10 0 24 82 cyclohexenone 70% 2- methylfuran Example 12 20% 3-Ethyl-2- 20 Ti-MCM-41 20 0 24 90 cyclohexenone 80% 2- methylfuran Example 13 30% 20 TiO₂/SiO₂ 10 10 10 85 cyclopentenone 70% 2- methylfuran Example 14 40% of 3-methyl- 20 TiO₂/SiO₂ 10 10 9 80 2-cyclopentenone 60% 2- methylfuran Example 15 30% of 4,4′- 20 TiO₂/MK-10 10 0 9 86 dimethyl-2- cyclopentenone 70% 2- methylfuran Example 16 30% of 3,4,5- 20 TiO₂/MK-10 10 0 12 90 trimethyl-2- cyclopentenone 70% 2- methylfuran Example 17 20% 20 ZnO/HY 5 15 9 93 cyclohexenone 80% 2,3- dimethylfuran Example 18 30% 3-methyl-2- 20 ZnO/HY 5 15 9 89 cyclohexenone 70% 2,3- dimethylfuran Example 19 30% 3,5- 20 TiO₂/SBA-15 5 0 9 83 dimethyl-2- cyclohexenone 70% 2,4- dimethylfuran Example 20 20% 2,3,5- 20 TiO₂/SBA-15 5 0 12 92 trimethyl-2- cyclohexenone 80% 2-ethylfuran Example 21 40% of 3-ethyl-2- 20 TiO₂/Al₂O₃ 5 20 9 84 cyclopentenone 60% 2,3- diethylfuran Example 22 10% 3-ethyl-2- 20 P25 5 20 9 92 cyclohexenone 90% 2,4- diethylfuran Example 23 40% 20 P25 10 −40 24 82 cyclohexenone 60% 2,5- diethylfuran Example 24 40% 20 ZnO/Hbeta 10 −40 24 85 cyclohexenone 60% 2,5- dimethylfuran Example 25 40% 20 ZnO/Hbeta 10 −40 24 88 cyclopentenone 60% 2,5- dimethylfuran Example 26 40% 20 ZnO/Hbeta 10 10 24 90 cyclopentenone 60% 2,5- dimethylfuran Example 27 40% 20 ZnO/C₃N₄ 10 10 24 91 cyclopentenone 60% 2,5- dimethylfuran Example 28 40% 20 TiO₂/C₃N₄ 10 10 24 85 cyclopentenone 60% 2,5- dimethylfuran Example 29 40% 20 ZnO/WO₃ 10 10 24 83 cyclopentenone 60% 2,5- dimethylfuran Example 30 40% 20 TiO₂/WO₃ 10 10 24 81 cyclopentenone 60% 2,5- dimethylfuran

The specific reaction steps are exemplified by Example 1 in Table 1: in a 25 mL single-port jacketed glass reactor, 6 g of cyclopentenone and 14 g of furan were added and bubbled with nitrogen gas for 0.5 h whiling being stirring, and then the reactor was sealed; a circulation with 10° C. water started and the reaction mixture was irradiated by a high-pressure mercury lamp for 24 h; the obtained fuel precursor molecules were analyzed by using gas chromatography-mass spectrometry, and the result shows that the yield of the target product, [2+4] cycloaddition fuel precursor molecule A, was 30%, and the others were the by-products of the [2+2] product B of the photochemical reaction of the cyclopentenone per se and the [2+2] product C of the photochemical reaction between the cyclopentenone and the furan; the reaction was described in the following scheme:

Example 2 was conducted by adding 2 g of a photocatalyst ZnO/HZSM-5 on the basis of Example 1, and the other reaction conditions were the same as those in Example 1. The results show that the yield of the fuel precursor molecules A was 90%. Clearly, adding the photocatalyst can significantly increase the selectivity to the target product of the Diels-Alder reaction. The reaction conditions and yields of Examples 3-30 were shown in Table 1. As seen from Table 1, the selectivity to the target product, the [2+4] cycloaddition fuel precursor molecules, of the photocatalytic Diels-Alder reaction was greatly improved.

Table 2 shows the reaction conditions and results of Examples 31 to 52 in which the fuel precursor molecules of Examples 1-30 in Table 1 were hydrodeoxygenated to produce the fused-ring alkane fuels (the fuel precursor molecules obtained in Examples 1 and 2 have the same structure; the fuel precursor molecules obtained in Examples 10, 11, and 12 have the same structure; the fuel precursor molecules obtained in Examples 25, 26, 27, 28, 29 and 30 have the same structure).

TABLE 2 Hydrodeoxygenation Reaction of Fuel Precursor Molecules Reactant (fuel precursor Hydrogen Reaction Reaction Serial No. molecules 20 g) Catalyst (mass) pressure/MPa temperature/° C. time/h Example 31 Example 1 5 g Pd/HY 6 200 24 Example 32 Example 3 5 g Pd/Hβ 6 200 24 Example 33 Example 4 5 g Pd/HZSM-5 6 200 24 Example 34 Example 5 5 g Pt/HZSM-5 6 200 48 Example 35 Example 6 5 g Pt/HY 6 200 48 Example 36 Example 7 5 g Pt/Hβ 6 200 48 Example 37 Example 8 8 g Ni/HZSM-5 8 250 48 Example 38 Example 9 8 g Ni/HY 8 250 48 Example 39 Example 10 8 g Ni/Hβ 8 250 48 Example 40 Example 13 8 g Cu/HZSM-5 8 280 48 Example 41 Example 14 8 g Cu/HY 8 280 48 Example 42 Example 15 8 g Cu/Hβ 8 280 48 Example 43 Example 16 5 g Au/HZSM-5 4 200 48 Example 44 Example 17 5 g Au/HY 4 200 48 Example 45 Example 18 5 g Au/Hβ 4 200 24 Example 46 Example 19 5 g Pd/SBA-15 6 200 24 Example 47 Example 20 5 g Pt/SBA-15 6 200 24 Example 48 Example 21 5 g Au/SBA-15 6 200 24 Example 49 Example 22 8 g Ni/SiO₂ 8 200 48 Example 50 Example 23 5 g Pd/HY 6 200 24 Example 51 Example 24 5 g Pd/HZSM-5 6 200 24 Example 52 Example 25 8 g Ni/HZSM-5 8 250 24

The hydrodeoxygenation reaction of the fuel precursor molecules is exemplified by Example 35 of Table 2, and the specific steps are described as follows: a 100 mL autoclave were charged with 20 g of the fuel precursor molecules obtained in Example 6 and 5 g of a catalyst Pd/HZSM-5, sealed, replaced with N₂for three times, and then charged with 6 MPa of H₂, and the mixture was raised to temperature 200° C. with stirring and reacted for 24 h; the reaction solution was analyzed by using gas chromatography-mass spectrometry, to qualitatively determine the product and calculate the reaction yield; the fuel precursor molecules were fully converted, and the target product of fused ring alkaline fuel molecules has the yield of 91%; the reaction conditions and product yields of the other examples are shown in Table 2.

The fused-ring alkane fuel obtained in Example 35 was measured to have a density of 0.896 g/cm³, a freezing point of less than −70° C., and a mass heat value of 42.4 MJ/kg. The measurement results of the fused-ring alkane fuels obtained in the other examples are shown in Table 3.

TABLE 3 Properties of Fused-ring alkane Fuels Obtained in Examples 31-52 Density Freezing point Mass heat value Serial No. (g/cm³) (° C.) (MJ/kg) Example 31 0.883 −52 42.1 Example 32 0.879 −60 42.3 Example 33 0.875 −60 42.5 Example 34 0.906 −57 42.3 Example 35 0.896 <−70 42.4 Example 36 0.892 <−70 42.5 Example 37 0.890 <−70 42.7 Example 38 0.887 <−70 42.8 Example 39 0.886 <−70 43.1 Example 40 0.880 −63 42.3 Example 41 0.876 −70 42.4 Example 42 0.876 −68 42.4 Example 43 0.872 <−70 43.2 Example 44 0.884 −68 42.5 Example 45 0.880 <−70 42.9 Example 46 0.881 <−70 43.0 Example 47 0.876 <−70 42.9 Example 48 0.874 <−70 43.4 Example 49 0.872 <−70 43.5 Example 50 0.872 <−70 43.1 Example 51 0.885 −60 42.4 Example 52 0.875 <−70 42.5

From the above results, it can be seen that a substituted or unsubstituted furan and a substituted or unsubstituted cycloenones may prepare the fused-ring alkane fuels in a high selectivity and a high yield through a heterogeneous photocatalytic Diels-Alder cycloaddition reaction and then through a hydrodeoxygenation reaction. The resultant fused-ring alkane fuels have excellent performances of high density, high heat value, low freezing point, and high thermal stability.

Claims

1. (canceled)

2. (canceled)

3. A process for preparing a fused-ring alkane fuel, wherein the fused-ring alkane fuel has the following structure:

wherein n is 1 or 2; R1, R2, R3, R4 and R5 are H or —CH3 or —CH2CH3;

the fused-ring alkane fuel has a density of greater than 0.870 g/cm3, a freezing point of not higher than −50° C., and a net mass heat value of not less than 42.0 MJ/kg; and

the process for preparing a fused-ring alkane fuel, wherein the process comprises steps of:

(1) in a presence of ultraviolet light and a photocatalyst, a Diels-Alder cycloaddition reaction between a substituted or unsubstituted cyclic enone and a substituted or unsubstituted furan molecule occurs to produce a fuel precursor molecule:

(2) the fuel precursor molecule obtained in the step (1) is subjected to hydrodeoxygenation to produce the fused-ring alkane fuel.

4. The process according to claim 3, wherein the photocatalyst in the step (1) is one or more selected from the group consisting of ZnO/HZSM-5, ZnO/Na-ZSM, ZnO/Hfβ, ZnO/HY, ZnO/LaY, Ti-MCM-41, TiO2/Al2O3, TiO2/SiO2, TiO2/MK-10, TiO2/SBA-15, P25, ZnO/C3N4, TiO2/C3N4, ZnO/WO3, TiO2/WO3, C3N4, WO3, and WO2.72, wherein the photocatalyst is added in an amount of 1% to 20% by weight of reactants; a reaction temperature ranges from −40° C. and 30° C., and a reaction time ranges from 9 h to 24 h.

5. The process according to claim 3, wherein the substituted or unsubstituted cyclic enone in the step (1) is one or more selected from the group consisting of cyclopentenone, 3-methyl-2-cyclopentenone, 4-methyl-2-cyclopentenone, 5-methyl-2-cyclopentenone, 4,4′-dimethyl-2-cyclopentenone, 3,4-dimethyl-2-cyclopentenone, 3,5-dimethyl-2-cyclopentenone, 4,5-dimethyl-2-cyclopentenone, 3,4,4′-trimethyl-2-cyclopentenone, 3,4,5-trimethyl-2-cyclopentenone, 3-ethyl-2-cyclopentenone, 4-ethyl-2-cyclopentenone, 5-ethyl-2-cyclopentenone, 4,4′-diethyl-2-cyclopentenone, 3,4-diethyl-2-cyclopentenone, 3,5-diethyl-2-cyclopentenone, 4,5-diethyl-2-cyclopentenone, 3,4,4′-triethyl-2-cyclopentenone, 3,4,5-triethyl-2-cyclopentenone, cyclohexenone, 2-methyl-2-cyclohexenone, 3-methyl-2-cyclohexenone, 4-methyl-2-cyclohexenone, 5-methyl-2-cyclohexenone, 6-methyl-2-cyclohexenone, 2,3-dimethyl-2-cyclohexenone, 2,4-dimethyl-2-cyclohexenone, 2,5-dimethyl-2-cyclohexenone, 2,6-dimethyl-2-cyclohexenone, 3,4-dimethyl-2-cyclohexenone, 3,5-dimethyl-2-cyclohexenone, 3,6-dimethyl-2-cyclohexenone, 4,5-dimethyl-2-cyclohexenone, 4,6-dimethyl-2-cyclohexenone, 5,6-dimethyl-2-cyclohexenone, 2-ethyl-2-cyclohexenone, 3-ethyl-2-cyclohexenone, 4-ethyl-2-cyclohexenone, 5-ethyl-2-cyclohexenone, 6-ethyl-2-cyclohexenone, 2,3-diethyl-2-cyclohexenone, 2,4-diethyl-2-cyclohexenone, 2,5-diethyl-2-cyclohexenone, 2,6-diethyl-2-cyclohexenone, 3,4-diethyl-2-cyclohexenone, 3,5-diethyl-2-cyclohexenone, 3,6-diethyl-2-cyclohexenone, 4,5-diethyl-2-cyclohexenone, 4,6-diethyl-2-cyclohexenone, 5,6-diethyl-2-cyclohexenone, 2,3,4-trimethyl-2-cyclohexenone, 2,3,5-trimethyl-2-cyclohexenone, 2,3,6-trimethyl-2-cyclohexenone, 3,4,5-trimethyl-2-cyclohexenone, 3,4,6-trimethyl-2-cyclohexenone, 4,5,6-trimethyl-2-cyclohexenone, and 4,5,6-trimethyl-2-cyclohexenone;

the substituted or unsubstituted furan is one or more selected from the group consisting of furan, 2-methylfuran, 3-methylfuran, 2,3-dimethylfuran, 2,4-dimethylfuran, 2,5-dimethylfuran, 2-ethylfuran, 3-ethylfuran, 2,3-diethylfuran, 2,4-diethylfuran and 2,5-diethylfuran;

wherein the substituted or unsubstituted cyclic enone is not higher than 40 wt % based on a total mass of the substituted or unsubstituted cyclic enone and the substituted or unsubstituted furan.

6. The process according to claim 3, wherein the fuel precursor molecule in the step (2) is hydrodeoxygenated under the following conditions: in a presence of a hydrodeoxygenation catalyst, a reaction temperature of 200° C. to 280° C., a hydrogen gas pressure of 4 MPa to 8 MPa, and a reaction time of 24 h to 48 h.

7. The process according to claim 6, wherein the hydrodeoxygenation catalyst is one or more of copper, nickel, platinum, gold or palladium loaded on one or more of supporters Al2O3, SiO2, HZSM-5, MCM-41, Hβ, SBA-15 or HY; the hydrodeoxygenation catalyst is added in an amount of 1% to 40% by weight of the fuel precursor molecule.

8. The process according to claim 3, wherein the ultraviolet light in the step (1) is a light having a wavelength between 300 nm and 360 nm.

9. The process according to claim 3, wherein the photocatalyst in the step (1) increases a selectivity to a target product of the Diels-Alder cycloaddition reaction between the substituted or unsubstituted cyclic enone and the substituted or unsubstituted furan molecule.

10. The process according to claim 4, wherein the ultraviolet light in the step (1) is a light having a wavelength between 300 nm and 360 nm.

11. The process according to claim 4, wherein the photocatalyst in the step (1) increases a selectivity to a target product of the Diels-Alder cycloaddition reaction between the substituted or unsubstituted cyclic enone and the substituted or unsubstituted furan molecule.