Magnetic Catalyst Research Articles

In situ decorated pd NPs on Triazin-encapsulated Fe3O4/SiO2-NH2 as magnetic catalyst for the synthesis of diaryl ethers and oxidation of sulfides

This article is devoted to the synthesis of a new magnetic palladium catalyst that has been immobilized on A-TT-Pd coated-magnetic Fe3O4 nanoparticles. Such surface functionalization of magnetic particles is a promising method to bridge the gap between heterogeneous and homogeneous catalysis approaches. The structure, morphology, and physicochemical properties of the particles were characterized through different analytical techniques, including TEM, FT-IR, XRD, SEM, EDS, TGA-DTG, ICP, and VSM techniques. The obtained Fe3O4@SiO2@A-TT-Pd performance can show excellent catalytic activity for the synthesis of diaryl ethers and oxidation of sulfides, and the corresponding products were obtained with high yields. The advantages of this catalyst include a simple test method, green reaction conditions, no use of dangerous solvents, short reaction time, low catalyst loading, and reusability. Also, the nanocatalyst was easily separated from the reaction mixture with the help of a bar magnet and recovered and reused several times without loss of stability and activity.

Improved Reductive Catalytic Fractionation of Lignocellulosic Biomass through the Application of a Recyclable Magnetic Catalyst

Improved Reductive Catalytic Fractionation of Lignocellulosic Biomass through the Application of a Recyclable Magnetic Catalyst

CO2 plasma inducing steel-slag with active sites for efficient growth of carbon nanotubes for the high-performance microwave absorption

As a solid waste generated in the metallurgical process, the highly efficient catalysis of steel-slag for carbon nanotube (CNT) growth remains a huge challenge. Herein, a CO2 plasma-inducing approach for modifying the steel-slag catalyst with rich active sites was developed for CNT growth in the chemical vapor deposition (CVD) process. Furthermore, the high-energy CO2 plasma refines the particles on the steel-slag surface, reducing the particle size on the surface of steel-slag effectively increasing the active sites of the catalyst. In addition, the thermal effect generated by the gas molecule ionization process under CO2 increases the background temperature of the steel-slag, and the interaction between the oxygen-active substances produced and the iron oxide on the surface of steel-slag undergoes an oxidation reaction upon full contact with high-energy particles, which greatly improves the catalytic efficiency of the steel-slag as a catalyst for CNT, and increases the catalytic efficiency by 50 % compared with the non-plasma modified steel-slag as a catalyst for catalyzing CNTs. In addition, catalytically grown CNTs encapsulate magnetic steel-slag catalysts to form a three-dimensional CNT network structure, with high-performance electromagnetic wave absorption. The composite absorbing material with a thickness of only 3.55 mm has a minimum absorption rate of −64.08 dB for electromagnetic waves at a frequency of 7.9 GHz. The dielectric and the magnetic loss of steel-slag lead to enhanced electromagnetic wave absorption. Therefore, this study provides an inexpensive and environmentally friendly idea for the design of high-efficiency CNT growth and solid waste catalyst modification synthesized with high-performance absorbers.

Recent Advances in Magnetic Nanoparticle-Based Heterogeneous Catalysts for Efficient Biodiesel Production: A Review

Recent Advances in Magnetic Nanoparticle-Based Heterogeneous Catalysts for Efficient Biodiesel Production: A Review

Conversion of waste paper sludge into magnetic biochar for activation of peroxydisulfate for tetracycline removal

ABSTRACT The Fe2+-peroxydisulfate (PDS) process is an effective method to enhance paper sludge dewaterability. However, the generated waste of iron-rich sludge cake needs to be disposed of properly. Converting sludge cake into magnetic biochar catalysts can help to shorten its environmental risks, recover resources, and reduce catalyst costs. In this work, the magnetic sludge biochar (Fe-SBC) was prepared and applied as a PDS activator to remove tetracycline (TC). Results showed that the Fe-SBC pyrolyzed at 600 °C presented excellent catalytic activity for PDS to degrade TC (rate of 74.89%) under the optimum conditions (intrinsic pH, 10 mM PDS, 0.5 g/L Fe-SBC, and 50 mg/L TC). It was found for the first time that the addition sequences of the biochar catalyst and PDS were insignificant on TC removal. Furthermore, the TC removal mechanism was proposed to be free radicals (·OH, SO4·−, and O2−·) and non-radical (1O2) pathways working together for TC removal, for which 1O2 was dominated. In addition, coexisting ions (Cl− and CO32−) had an inhibitory effect on TC degradation. This work will provide a new recycling approach for waste paper sludge in wastewater treatment.

A New Powerful Magnetic Dark Catalyst Based on rGO/Fe3O4/CdSe Nanocomposite for Ultrafast Degradation of Methylene Blue Dye.

In the present study, Rgo/Fe3O4/CdSe as a dark catalyst material was synthesized by a refluxing method. The synthesized magnetic nanocomposites were studied by various analyses such as Fourier transform infrared (FTIR), energy-dispersive X-ray spectroscopy (EDS), field emission scanning electron microscopy (FESEM), X-ray diffractometer (XRD), Raman, Zeta and vibrating sample magnetometer (VSM). Characterization of structural analysis showed that the nanocomposites were successfully synthesized. The absorption spectrum was used to determine the dark catalyst activity of rGO/Fe3O4/CdSe nanocomposite. Analysis of the absorption spectrum showed that the prepared nanocomposites degrade the MB organic dye completely (100%) after 2min of stirring in the dark, also experimenting with different pH showed that the best performance for the degradation of MB occurs in neutral and alkaline media. The Raman spectrum analysis showed that the Fe3O4/CdSe quantum dots (QDs) were correctly incorporated on the reduced graphene oxide (rGO) nanosheets. Zeta potential analysis showed that rGO/Fe3O4/CdSe has a large amount of negative charge on its surface and the surface charge increased by about 16 mV compared to the Fe3O4/CdSe compound. BET and BJH techniques were used to determine the effective surface area and pore size diameter, BET results to determine the effective surface area showed that by adding graphene to the compound, the specific surface area increased from 42.877 m2g-1 to 54.1896 m2g-1. The radical scavenger experiment showed that electrons play an essential role in the degradation process. VSM analysis showed that the prepared nanocomposites have excellent superparamagnetic behavior, this advantage enables the easy collection of nanocatalysts by magnets from wastewater after dye degradation.

Novel and reusable magnetic MOF nanocomposite coupled ionic liquid- promoted efficient chemical fixation of CO2 into α-alkylidene cyclic carbonates

Carbon dioxide as a C1 building block to synthesize α-alkylidene cyclic carbonates is an environmental and sustainable approach. In this work, we designed and synthesized a type of multifunctional magnetic MOF nanocomposite catalysts, which could realize the carboxylic cyclization of CO2 and propargylic alcohols into α-alkylidene cyclic carbonates under solvent-free conditions. Among all the prepared nanocomposites, the MnFe2O4@SiO2@Cu-MOF nanocomposite is the best in catalytic activity combined with the tetrabutylphosphonium acetate ([Bu4P]OAc) ionic liquid cocatalyst. The catalytic system MnFe2O4@SiO2@Cu-MOF/[Bu4P]OAc displayed excellent performance in catalyzing the carboxylic cyclization of CO2 and different propargylic alcohols, and a series of α-alkylidene cyclic carbonates were obtained in high to excellent yields (88 ∼ 98 %) under mild reaction conditions (0.2 MPa, 35 °C). In addition, the two-component catalytic system had high stability and reusability, and can be easily separated and reused up to six consecutive cycles without considerable decrease in catalytic activity. Moreover, using the ionic liquid [Bu4P]OAc as the cocatalyst, the nanocomposite had good substrate adaptability for the catalytic carboxylic cyclization, which opens interesting prospects for the development of new magnetic MOF nanocomposites as efficient heterogeneous catalysts for the chemical transformation of CO2 into value-added chemicals.

Development and fabrication of graphene oxide and reduced graphene oxide incorporated MnFe2O4@Bi2WO6 nanocomposite for efficient degradation of antibiotic drug as water contaminant under visible-light illumination

Tetracyclines are one category of extensively applied antibiotics. Meantime, owing to misapplication and inappropriate disposal, they are mostly discovered in wastewater, which causes a series of environmental contamination and stated a threat to a person's health and security. The present study investigates the photodegradation of tetracycline using MnFe2O4@Bi2WO6/graphene oxide, GO, and MnFe2O4@Bi2WO6/reduced graphene oxide, RGO, and MnFe2O4@Bi2WO6 nanocomposites as permanent photocatalyst with the aid of visible light. A facile microwave assisted combustion method was applied in solid state rapidly, conveniently to fabricate MnFe2O4@ Bi2WO6–GO and MnFe2O4@ Bi2WO6–rGO nanocomposites at low power 150 W and in time 10 min with very low amount of glycine (as fuel). Consequently, XRD, EDX Mapping, DRS, PL, TEM, FESEM, FTIR, VSM, BET and UV–Visible spectrophotometric analysis demonstrated characteristic of nanocomposites and specifications of existent photocatalyst. Magnetic investigations revealed that the MnFe2O4@ Bi2WO6-GO and MnFe2O4@ Bi2WO6–RGO nanocomposites can be easily separated from the solution by an external magnetic field. MnFe2O4@ Bi2WO6–GO nanocomposites were discovered with high specific surface area 73.83 m2/g than MnFe2O4@Bi2WO6–RGO nanocomposites with specific surface area 17.75 m2/g. Highest photocatalytic activity was determined for the MnFe2O4@ Bi2WO6–GO (catalyst-0.10 g/l, tetracycline antibiotic concentration 10 mg/l and at pH = 4) within 25 min of visible light irradiation without using any oxidizing agent. The investigation of kinetic study revealed that kinetic parameter specified to photodegradation and experimental outcomes follow first-order model. the superoxide, hydroxyl radicals, ℎ+ holes and light are the principal demonstrates of the reaction mechanism for the effective degradation of tetracycline drug. The evaluation of MnFe2O4@ Bi2WO6–GO and MnFe2O4@ Bi2WO6–RGO magnetic catalysts has proposed the encouraging and significant role of nanocomposites in perilous pharmaceuticals refinement from industrial wastewater and also, magnetically photocatalyst attributes can be used as a potent separable tool for eliminating water pollution problems in the various industry.

Enhanced Magnetic Heating for Efficient Oxygen Evolution Reaction by Pinning Effect of Ferromagnetic/Antiferromagnetic Coupling.

The magnetic heating effect under alternating magnetic fields (AMFs) has recently gained attention in catalysis due to its potential to greatly boost catalytic activities by providing localized heating around magnetic nanoparticles. However, nanoparticles still suffer from low magnetic heating efficiency due to their low magnetic anisotropy and thermal fluctuation, which is a key barrier in the wide application of AMF-assisted catalysis. Herein, by introducing the pinning effect of ferromagnetic/antiferromagnetic (FM/AFM) coupling, NiO/NiOOH (AFM/FM) core-shell nanoparticles exhibit significantly enhanced oxygen evolution reaction activity and resistance to thermal fluctuations under AMF, compared to NiOOH nanoparticles. Notably, magnetized NiO/NiOOH nanoparticles provide an overpotential of 186 mV at 10 mA cm-2, outperforming unmagnetized ones (218 mV) under the same conditions, further emphasizing the prominent role of the pinning effect in enhanced magnetic heating efficiency. This work provides valuable inspiration to design advanced magnetic catalysts and meet the challenge of the development of AMF-assisted catalysis.

Structural, magnetic and electrical studies on nickel doped copper ferrite synthesized using sol-gel method

Nickel doped copper ferrite nanoparticles NixCu1-xFe2O4(x = 0.1, 0.3, 0.5, 0.7, and 0.9) have been prepared through well known sol-gel technique. Numerous analytical methods, including the Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM), and powder X-ray diffractometer (XRD), were used to analyze the synthesized materials. Synthesized sample XRD patterns reveal the single phase development of the spinel crystalline structure in the absence of any contaminant. The concentration of Ni ions rises with a corresponding decrease in crystallite size. Scanning electron microscopy (SEM) was also used to assess the microstructure. By using UV–Visible spectrometer an optical absorbance and through FTIR, two of ferrite's distinctive bands were verified. The M-H loops show that when the concentration of nickel ions increases, saturation magnetization varies. The Cyclic-Voltameter was used to perform the ionic electrochemical analysis. The NixCu1-xFe2O4 nanopowder's enhanced magnetic characteristics suggest that these substances would make good candidates for magnetic catalysts.

Cu(II) complex heterogenized on magnetic mesoporous nanocomposite (SBA-16@Fe3O4) as an efficient catalyst for the reduction of nitro compounds

In the present study, a novel magnetic heterogeneous copper catalyst was developed by the immobilization of a Cu(II) complex on the surface of magnetic mesoporous nanocomposite (SBA-16@Fe3O4) through post-synthetic method. The synthesized catalyst was analyzed by various characterization methods including FT-IR, EDS, XRD, Nitrogen physisorption, TEM, TGA, VSM, and ICP-OES. After complete characterization, its catalytic efficiency was evaluated in the hydrogenation of nitroarenes to amines. Taking the nitrobenzene reduction of as an example of a reaction, the reaction conditions were optimized by changing diverse parameters like solvent, temperature, time, amount of catalyst, as well as the type and amount of hydrogen source. The catalyst revealed highly efficient catalytic activity in the hydrogenation of numerous nitroarenes to the corresponding aminoarenes in pure water as the solvent with sodium borohydride as a H2 source at room temperature. Additionally, the catalyst could be simply recovered from the mixture of reaction via magnetic separation and was able to mediate the reaction for multiple times with undiminished catalytic performance.

Catalytic ethanolysis of Xiaojihan subbituminous coal to platform chemicals enhanced by pre-oxidation with ozone

Xiaojihan subbituminous coal (XSBC) was pre-oxidized by ozone to prepare oxidized XSBC (OXSBC). Then, the ethanolysis was conducted on OXSBC at 300 °C under an initial nitrogen pressure (INP) of 1 MPa for 2 h. On this basis, the influences of pre-oxidation conditions on the content of oxygen-containing functional groups and the yield of soluble portion (SP) from the ethanolysis of XSBC and OXSBC were explored. The research results show that the yield of SP from the OXSBC ethanolysis is higher than that from the XSBC ethanolysis, and the highest yield of SP from the OXSBC ethanolysis reaches 24.9 wt% at 50 °C for 3 h, an increase of 80.4 % compared to the yield of SP from the XSBC ethanolysis. Besides, the magnetic nanosphere Co-CuFe2O4 catalyst, prepared by adopting the one-pot hydrothermal method, was applied to the catalytic ethanolysis (CE) of OXSBC3 at 300 °C, 1 MPa INP, and 2 h. The catalyst is noticeably active in the CE of OXSBC3, as it promotes the yields of SP and oxygen-containing organic compounds obtained from the OXSBC3 ethanolysis from 24.9 wt% and 76.25 mg g−1 to 42.8 wt% and 204.16 mg g−1, respectively. The CE of the model compound demonstrates that ethanol is activated by Co-CuFe2O4 to release H+, H-, and +CH2CH3, which play a crucial role in the conversion of benzyloxybenzene. This study provides a novel approach for acquiring value-added organic chemicals from low-rank coals.

Photocatalytic degradation of methylene blue in aqueous media using magnesium-substituted copper ferrite as a magnetic catalyst

In this study, copper nanosized ferrites substituted with magnesium ions were synthesized using the sol-gel self-combustion method, with polyethylene glycol (MW 2000) serving as both fuel and chelating agent. Structural properties were investigated using X-ray diffraction. It was confirmed that all samples crystallized as cubic spinels with space group Fd3m. Optical studies showed band gaps increasing from 1.51 eV for CuFe2O4 to 1.62 eV for MgFe2O4, suggesting modifications in electronic structure due to magnesium substitution. Photocatalytic studies revealed that CuFe2O4 exhibited the most efficient degradation of Methylene Blue dye, with near-complete degradation at 160 minutes. Magnesium-substituted samples (x = 0.4 and x = 0.6) also showed significant degradation, though at a slower rate compared to pure CuFe2O4. Photocatalytic performance, particularly in degrading Methylene Blue, was evaluated using various kinetic models such as First- and Second-Order Kinetics, the Langmuir-Hinshelwood model, and the two-parameter Weibull distribution.

Synergistic magnetic Cu-Fe catalysts on N-doped biochar for efficient alkali lignin catalytic depolymerization into monophenols

Alkali lignin, a major by-product of papermaking, poses disposal challenges, hindering the full valorization of lignocellulose in sustainable biorefineries. One-pot lignin catalytic depolymerization (LDP) in water offers a promising route for producing valuable phenolic compounds. This study reports the successful synthesis of in-situ N-doped biochar supported CuxFey catalysts (CuxFey/N-BC) via a one-step carbothermal reduction method, enabling LDP in water without the need for external hydrogen, additives, alcohol solvent, or co-catalysts. Notably, the Cu5Fe1/N-BC could achieve remarkable catalytic performance under mild reaction conditions (280 °C, 6 h, 18 mL water), yielding 80.84±2.23 mg/g of monophenol, 56.17±1.32 % of bio-oil, and a lignin conversion rate of 80.66±0.73 %. This significantly surpassed the performance of monometallic catalysts and bare biochar. The synergistic effects of intermetallic interactions and nitrogen doping were proposed to create abundant active sites and rich pore structures, promoting efficient LDP reactions. Furthermore, the Cu5Fe1/N-BC exhibited excellent recyclability, with minimal activity loss (2.79 %) per cycle, due to its strong magnetism and favorable interactions. Mechanism investigation revealed that the Cu5Fe1/N-BC efficiently cleaved the C-O and C-C bonds in lignin, and led to the targeted production of guaiacyl phenols. This study provides valuable insights and practical strategy for valorizing lignin into valuable chemicals, advancing its utilization in various applications.

Regulating the N-functional hydrogen bond donors over magnetic nanoparticles supported imidazole tribromide zinc ionic liquid for CO2 cycloaddition

The design of catalysts for the mile production of cyclic carbonates by CO2 cycloaddition is of value. Magnetic polymer nanoparticles-supported imidazole tribromide zinc ionic liquid catalysts, incorporating N-functional hydrogen bond donors (HBD), was successfully accomplished. The correlation between the N-functional HBD and catalytic activity was thoroughly investigated through experimental studies and DFT calculations. The catalyst featuring a secondary amine group (NHM) demonstrated remarkable catalytic performance in CO2 cycloaddition reactions. Under optimized conditions, including 0.12 mol% catalyst dose, 100 °C, and nPO:nCO2 = 1:1.2 for 3 h, a complete conversion was achieved. The exceptional performance of the catalyst was attributed to the multicenter synergistic effect, arising from the appropriate electronegativity, minimal spatial site resistance, a balanced distance between the NHM and imidazolium ion, and the presence of multiple active centers (NHM, Zn2+, and Br−). The integration of a magnetic component enabled swift separation and exceptional recovery stability over 8 consecutive cycles.

Three-component Synthesis of Tetrahydrobenzo[b]pyrans Using MMWCNTs-PEG-IL as a Novel Magnetic Immobilized Ionic Liquid

Introduction: A novel immobilized imidazolium type ionic liquid was synthesized using poly(ethylene glycol) (PEG) functionalized magnetic multi-walled carbon nanotubes. This immobilized ionic liquid (MMWCNTs-PEG-IL) was characterized by FT-IR, VSM, XRD, FE-SEM and EDX analysis. Method: Then, it was used as a magnetic catalyst in a three-component reaction to yield tetrahydrobenzo[b]pyran derivatives. First, optimized reaction conditions were investigated. A mixture of containing dimedone (1 mmol), malononitrile (1 mmol), benzaldehyde (1.2 mmol) and MMWCNTs-PEG-IL (0.03 g) in H2O/EtOH (5 mL) was stirred at 70 °C. After completion of the reaction, the mixture was cooled. Results: Then, an external magnet was used to separate the magnetic catalyst. This method has many advantages including high reaction yields, high TOFs, using non-toxic solvents, easy handling of catalyst, simple separation of catalyst from reaction medium and short reaction times. Conclusion: Also, the reusability of the magnetic catalyst has been investigated in 7 runs without serious loss of reaction yield.

A perspective on magnetic field-enhanced electrocatalytic water splitting

Magnetic field effects have received widespread attention due to their ability to enhance the process of water splitting at multiple scales. However, a systematic and comprehensive understanding of the source of the magnetic effect and the magnetic modulation of magnetic catalysts is lacking. This perspective focuses on recent advancements in harnessing external magnetic field to improve electrocatalytic water splitting and suggests future directions. First, the mechanism of several magnetic effects and their effects on water splitting are elaborated in detail, including the magnetohydrodynamic effect, magnetothermal effect, spin polarization effect, and magnetoresistance effect. Then, the classification and construction strategies of magnetic effect catalysts are summarized, primarily divided into single metal/alloy catalysts, metal oxide-based catalysts, and other magnetic catalysts. Finally, the challenges and potential perspective of magnetic field-enhanced water splitting are discussed, including mechanism study, in situ characterization, and multi-field synergy effects.

Photocatalytic degradation of the remazol red ultra RGB dye using SrFe12O19-Fe3O4 magnetic oxides dispersed in silica: Effect of reduction temperature

Dyes are the most frequently discarded industrial wastes in aquatic ecosystems, among which Remazol Red ultra RGB stands out. In this context, magnetic iron-based catalyst dispersed in silica were prepared by Pechini route as an alternative for the photodegradation of Remazol Red Ultra RGB. The XRD and Mössbauer spectroscopy results indicated the formation of a magnetic material that, after reduction treatment with H2, forms a magnetite phase combined with Sr hexaferrite dispersed in amorphous silica. The TPR-H2 profiles indicated the reduction of Fe3+ to Fe2+ within the considered temperature range, the amount of Fe2+ increased with rising temperature. The SEM images showed sponge-like morphology for the samples. The EDS spectra and mapping confirmed a high uniformity in the distribution of active iron species in the silica. The magnetic measurements showed a lower magnetic signal for the sample reduced at 600 °C, due to the lower magnetic moment of Fe2+ formed after the reduction. The diffuse reflectance spectra showed a main absorption region between 500 and 200 nm and the estimated band-gap values were of 1.4 and 1.9 eV for the reduced sample and the fresh oxide, respectively. The surface charge was obtained via zeta potential, demonstrating good stability under pH changes and reaching a negative potential in the pH range from 2 to 6. The photocatalytic tests showed that the samples with higher content of Fe2+ demonstrated a greater photocatalytic degradation of the Remazol Red Ultra RGB dye, reaching 100 % degradation in 1 h for the solid reduced at 600 °C. A plausible mechanism for the photodegradation of Remazol Red Ultra RGB was proposed, considering the different elementary steps involving the participation of iron sites and the formation of oxidant radicals.

Heterogeneous Photo-Fenton Degradation of Azo Dyes over a Magnetite-Based Catalyst: Kinetic and Thermodynamic Studies

Textile wastewater containing dyes poses significant environmental hazards. Advanced oxidative processes, especially the heterogeneous photo-Fenton process, are effective in degrading a wide range of contaminants due to high conversion rates and ease of catalyst recovery. This study evaluates the heterogeneous photodegradation of the azo dyes Acid Red 18 (AR18), Acid Red 66 (AR66), and Orange 2 (OR2) using magnetite as a catalyst. The magnetic catalyst was synthesized via a hydrothermal process at 150 °C. Experiments were conducted at room temperature, investigating the effect of catalyst dosage, pH, and initial concentrations of H2O2 and AR18 dye. Kinetic and thermodynamic studies were performed at 25, 40, and 60 °C for the three azo dyes (AR18, AR66, and OR2) and the effect of the dye structures on the degradation efficiency was investigated. At 25 °C for 0.33 mmolL−1 of dye at pH 3.0, using 1.4 gL−1 of the catalyst and 60 mgL−1 of H2O2 under UV radiation of 16.7 mWcm−2, the catalyst showed 62.3% degradation for AR18, 79.6% for AR66, and 83.8% for OR2 in 180 min of reaction. The oxidation of azo dyes under these conditions is spontaneous and endothermic. The pseudo-first-order kinetic constants indicated a strong temperature dependence with an order of reactivity of the type OR2 > AR66 > AR18, which is associated with the molecular size, steric hindrance, aromatic conjugation, electrostatic repulsion, and nature of the acid–base interactions on the catalytic surface.

Superhydrophobic and superacid magnetic catalyst induced highly selective aldol condensation and alkylation for high-density biofuels

Aldol condensation and hydroxyalkylation/alkylation reactions are the most widely used C–C coupling strategies to synthesize high-density biofuels. But their in-situ generated water is unavoidable and can reduce the acidity of catalyst, thereby inhibiting catalytic activity or triggering side reactions. Herein, novel superhydrophobic and superacid magnetic catalyst Fe3O4@SiO2@F-SO3H is designed and synthesized through simple cladding and chemical grafting. This magnetic catalyst can withstand high temperature up to 215 °C and displays much better superhydrophobicity (contact angle of 155.3°) and lipophilicity (contact angle of 0°) than those of classical Amberlyst-15 and Nafion-212. Notably this catalyst exhibits excellent activity, selectivity and stability for both aldol condensation and hydroxyalkylation/alkylation reactions of lignocellulose derived cyclic ketones and furans. After hydrodeoxygenation, three high-density fuels with density of 0.825, 0.881 and 0.887 g/mL were achieved. This work illustrates an efficient and convenient strategy to achieve high-performance acidic catalyst for synthesizing high-density fuels.