Experimental Study on Fe3O4 Nanoparticle-Assisted Microwave Enhancing Heavy Oil

Nanoparticle-assisted microwave heating of heavy oil has the advantages of fast temperature rise and high thermal efficiency. Compared with traditional heating methods, it can reduce viscosity in a shorter time. In addition, the heavy components in the heavy oil are cracked into light components at high temperatures (this high temperature cannot be reached by conventional heating methods). This process is irreversible and avoids the problem of viscosity recovery of heavy oil after the temperature is reduced. Through absorbing microwave heating experiments, study the effect of nanoparticles on the improvement of the ability of heavy oil to absorb waves and raise temperature; through the heavy oil upgrading experiment and the four-component analysis experiment, the effect of adding hydrogen donor to assist microwave on the viscosity reduction of heavy oil upgrading by nanoparticles was studied, and the problem of viscosity recovery was determined; Through the gravity drainage experiment, the mechanism of nanoparticle-assisted microwave to improve the recovery of heavy oil is studied, and the influence of water content, nanocatalyst, and microwave power on the production of drainage is analyzed. The results show that nanoparticles can improve the wave absorption and heating capacity of heavy oil, and adding 0.6 wt% of nanomagnetic iron oxide catalyst can increase the heating rate of heavy oil in microwave by 60.6%; nanoparticle-assisted microwave heating method can effectively upgrade heavy oil and reduce viscosity. The experimental conditions are 2 wt% tetralin mass concentration, 0.5 wt% nano-Fe3O4 particle mass concentration, microwave heating time 50-60 min, and microwave power 539 W. Under this experimental condition, the viscosity is reduced by 40%. This method has viscosity recovery problems, but final viscosity reduction effect is still very significant. Obtaining the mechanism of nanoparticle-assisted microwave to enhance oil recovery, one of which is that nanoparticles improve the wave absorption and heating capacity of heavy oil and increase the heating speed of heavy oil; the second is that the nanoparticles form local high temperature under the action of microwave, which catalyzes the hydrocracking reaction between the heavy components in the heavy oil and the hydrogen donor, upgrading and reducing the viscosity of the heavy oil, and accelerating the production of heavy oil.

Non-Catalytic Dissolution of Biochar Obtained by Hydrothermal Carbonization of Sawdust in Hydrogen Donor Solvent

The production of fuel hydrocarbons from CO2-neutral raw materials is a promising task at present. The thermal dissolution of biochar obtained by the method of hydrothermal carbonization of sawdust was studied. The dissolution of biochar in tetralin (hydrogen donor solvent) was studied at different temperatures (350–450 °C) and with two types of dilution of the mixture with tetralin: 1/3 and 1/4. The process proceeded without a catalyst. It was found that the samples subjected to thermal dissolution at temperatures of 425–450 °C had the highest conversion and yield of liquid products. The reaction temperature also had a significant effect on the composition of liquid products. It was found that an increase in the reaction temperature led to a significant increase in benzenes, both in the direct and in the hexane fraction. A benzene yield of more than 50% was observed for both fractions at a temperature of 450 °C. It was also suggested that the possible positive effect of abietates on the homogenization of the reaction mixture contributed to high conversion in the process. The biochar/tetralin ratio effects the yield and composition of the liquid products as well. An increase in the tetralin concentration in the mixture during thermal dissolution led to an increase in the conversion and yield of hydrocarbon fractions for fuel purposes. This is undoubtedly due to the large amount of elemental hydrogen involved in the hydrogenation of the reaction mixture.

In Situ Hydrodeoxygenation of Lignin-Derived Phenols With Synergistic Effect Between the Bimetal and Nb2O5 Support

Nb2O5-supported bimetallic catalysts were prepared by the impregnation method applied for the in situ hydrogenation of guaiacol. Guaiacol can be effectively transformed into cyclohexanol over different bimetallic catalysts using alcohol as the hydrogen donor. Meanwhile, the effects of different hydrogen donors such as isopropanol, sec-pentanol, and ethylene glycol on in situ hydrogenation of guaiacol were investigated in detail, and the results showed that isopropanol is the best hydrogen supply solvent. Then, the dependence of Ni–Mn/Nb2O5 properties on metal loading, reaction time, reaction temperature, and reaction pressure was studied for the in situ hydrogenation of guaiacol by using isopropanol as the hydrogen donor. Guaiacol can be completely converted, and the yield of cyclohexanol reached 71.8% over Ni–Mn/Nb2O5 with isopropanol as the hydrogen donor at 200°C for 5 h. The structures and characteristics of better catalytic properties of the Ni–Mn/Nb2O5 catalyst were determined by BET, NH3-TPD, XRD, XPS, SEM, and TEM, and the results indicated the particle size of the metal was small (approximately 10 nm) and the metal particles are finely dispersed in the whole support. Therefore, a large number of medium acid sites were generated on the 10Ni-10Mn/Nb2O5 with a large specific surface area, which could increase the interface between the metal and the support and may be beneficial to the hydrodeoxygenation of guaiacol.

Energy Densification of Biomass-Derived Furfurals to Furanic Biofuels by Catalytic Hydrogenation and Hydrodeoxygenation Reactions

The concomitant hydrolysis and dehydration of biomass-derived cellulose and hemicellulose to furfural (FUR) and 5-(hydroxymethyl)furfural (HMF) under acid catalysis allows a dramatic reduction in the oxygen content of the parent sugar molecules with a 100% carbon economy. However, most applications of FUR or HMF necessitate synthetic modifications. Catalytic hydrogenation and hydrogenolysis have been recognized as efficient strategies for the selective deoxygenation and energy densification of biomass-derived furfurals generating water as the sole byproduct. Efficient and eco-friendly catalysts have been developed for the selective hydrogenation of furfurals affording renewable furanic compounds such as 2-methylfuran, 2,5-dimethylfuran and 2-methyltetrahydrofuran with potential applications as biofuel, solvent and chemical feedstock. Hydrogen gas or hydrogen donor molecules, required for the above processes, can also be renewably obtained from biomass using catalytic processes, enabling a circular economy. In this review, the recent developments in the energy densification of furfurals to furanic compounds of commercial significance are elaborated, emphasizing the role of catalyst and the reaction parameters employed. Critical discussion on sourcing hydrogen gas required for the processes, using hydrogen donor solvents, catalyst design and the potential markets of furanic intermediates have been made. Critical evaluations of the accomplishments and challenges in this field are also provided.