Q1 Research Application · Frontier Focus

Pulsed microwave induced super-heating in graphitic carbon domains drives high-efficiency 5-hydroxymethylfurfural synthesis

This Chemical Engineering Journal paper (2025) is indexed as a Xianghu equipment application case for XH-200A+ and XH-200A / XH-200C; key result: Yield 80%.

Paper ID 552
Application Focus Microwave catalysis, Microwave-responsive catalyst design, Carbon-material structure control, Biomass platform-molecule conversion, High-efficiency HMF synthesis
Key Result Yield 80%
Core Condition Power 400 W
Paper ID
552
Journal
Chemical Engineering Journal
Impact Factor
13.2
CAS Zone
Zone 1
Year
2025
Equipment Model
XH-200A+ XH-200A / XH-200C
Affiliations
Nanjing Tech University
Research Directions
Microwave catalysis Microwave-responsive catalyst design Carbon-material structure control Biomass platform-molecule conversion High-efficiency HMF synthesis

Fact Snapshot

  • Paper: Pulsed microwave induced super-heating in graphitic carbon domains drives high-efficiency 5-hydroxymethylfurfural synthesis
  • Equipment: XH-200A+ and XH-200A / XH-200C
  • Source: Chemical Engineering Journal, 2025
  • Research direction: microwave catalysis, microwave-responsive catalyst design, carbon-material structure control, and biomass platform-molecule conversion
  • Core conditions: Power 400 W
  • Key results: Yield 80% and Yield 91%

Research Abstract

Pulsed microwave induced super-heating in graphitic carbon domains drives high-efficiency 5-hydroxymethylfurfural synthesis was published in Chemical Engineering Journal (2025) and is indexed as a Xianghu Q1 application case for XH-200A+ and XH-200A / XH-200C. The source record connects it with microwave catalysis, microwave-responsive catalyst design, carbon-material structure control, and biomass platform-molecule conversion. Core operating conditions include Power 400 W. Key reported results include Yield 80% and Yield 91%.

Research Background and Problem

The paper is positioned around microwave catalysis, microwave-responsive catalyst design, and carbon-material structure control. The equipment record identifies XH-200A+ and XH-200A / XH-200C as the Xianghu instrument context for this application case. The source affiliation record includes Nanjing Tech University.

Equipment Use and Experimental Conditions

ItemParameter
Power400 W

Key Result

Yield 80%
Yield 91%
MetricResult
Yield80%
Yield91%

Evidence Details

Equipment-detail evidence

Equipment-detail evidence: magnetic stirring.

Equipment and method evidence

HMF synthesis from fructose was carried out in a microwave reactor (multimode MW reactor, XH-200A+, Beijing, Xianghu). In a typical procedure, 0.14 M fructose and 0.2 g catalyst were charged into 20 mL DMSO. The MW reactor used pulsed microwave inputs and the temperature is set to 160 oC. Magnetic stirring was applied throughout the reaction process.

Source evidence

It was found that the HMF yield reached approximately 80% under continuous mode for 15 min or pulse mode for 4 cycles. respectively. However, the energy efficiency of the pulse mode input was approximately 4 times higher than that of the continuous mode (pulse mode: 11.43 mmol/KJ·L·g; continuous mode: 3.46 mmol/KJ·L·g).

Source evidence

Upon 100 W microwave irradiation, the solid phase experienced preferential heating, with the center region reaching a temperature of 76 oC within 60 s. Subsequently, the heat slowly dissipated from the carbon powders to the surrounding liquid phase, causing bulk DMSO phase to reach a temperature of approximately 50 oC.

Source evidence

It can be also observed that the energy efficiency under 600 W&2 cycles condition was 13.9 mmol/KJ·L·g, surpassing the 11.4 mmol/KJ·L·g observed under 400 W&4 cycles conditions.

Microwave-method evidence

Microwave-method evidence: source values include 100 W, 42 °C.

Microwave-method evidence

Microwave-method evidence: source values include 30 s, 300 s.

Yield evidence

Yield evidence: source values include 80%, 4 fold.

Source evidence

However, with an increase to 4 input cycles, the Fe-SC PSV catalyst achieved a maximum yield of 91%, albeit with a decrease in energy efficiency to 8.7 mmol/KJ·L·g.

Source evidence

Under a catalyst dosage of 0.1 g, the reaction achieved a 64 mol% HMF yield while maintaining a high energy efficiency of 18.5 mmol/KJ·L·g.

Additional source evidence

Additional source evidence: source values include 80-200 nm. Entities: Fe-SC.

Mechanism / Method Highlights

  • Fe-catalyzed graphitic carbon domains are the key structural basis. Fe-SC PSV shows the highest graphitization degree, loose curled graphitic nanosheets of about 80-200 nm, and sulfonic groups grafted at graphitic edges.
  • The higher graphitization degree strengthens dielectric response; Fe-SC PSV shows higher epsilon-prime at 2.45 GHz, making it more efficient at absorbing and converting microwave energy.
  • Microwave energy preferentially dissipates in the solid phase and solid-liquid interface, producing localized overheating near catalytic active sites.
  • Pulsed microwave input better matches rapid reaction with slower mass transfer: the on-cycle creates local high temperature, while the off-cycle allows mass and heat redistribution.
  • Localized heating promotes rapid HMF formation from fructose and suppresses undesired side reactions, so the advantage comes from heat placement near reactive sites rather than simply raising the bulk temperature.

Application Value

  • The optimized Fe-SC PSV catalyst reaches 80 mol% HMF yield and 18.5 mmol/KJ·L·g energy efficiency over four pulsed cycles.
  • Both pulsed and continuous modes can reach about 80% HMF yield, but pulsed operation gives about four times the energy efficiency of continuous operation.
  • Preserves quantitative result evidence: Yield 80% and Yield 91%.
  • Maintains source-level evidence details: Equipment-detail evidence: magnetic stirring, Equipment and method evidence: HMF synthesis from fructose was carried out in a microwave reactor (multimode MW reactor, XH-200A+, Beijing, Xianghu). In a typical procedure, 0.14 M fructose and 0.2 g catalyst were charged into 20 mL DMSO. The MW reactor used pulsed microwave inputs and the temperature is set to 160 oC. Magnetic stirring was applied throughout the reaction process, Source evidence: It was found that the HMF yield reached approximately 80% under continuous mode for 15 min or pulse mode for 4 cycles. respectively. However, the energy efficiency of the pulse mode input was approximately 4 times higher than that of the continuous mode (pulse mode: 11.43 mmol/KJ·L·g; continuous mode: 3.46 mmol/KJ·L·g), and Source evidence: Upon 100 W microwave irradiation, the solid phase experienced preferential heating, with the center region reaching a temperature of 76 oC within 60 s. Subsequently, the heat slowly dissipated from the carbon powders to the surrounding liquid phase, causing bulk DMSO phase to reach a temperature of approximately 50 oC.

Related Equipment

FAQ

Which Xianghu instrument is covered by this page?
The structured source records XH-200A+ and XH-200A / XH-200C for this paper.
What is the main application direction?
The source tags this paper under microwave catalysis, microwave-responsive catalyst design, and carbon-material structure control.
Which publication does this case come from?
It comes from Chemical Engineering Journal (2025), DOI 10.1016/j.cej.2024.157402.
Citation
Pulsed microwave induced super-heating in graphitic carbon domains drives high-efficiency 5-hydroxymethylfurfural synthesis
Chemical Engineering Journal, 2025
DOI: 10.1016/j.cej.2024.157402