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- 材料测试与制备
- 材料测试
- 催化剂制备
- English
- Who we are
- Products
- Characterisation Services
- Reactor Design & Manufacturing
- Contact us

- 材料测试与制备
- 材料测试
- 催化剂制备
- English
- Who we are
- Products
- Characterisation Services
- Reactor Design & Manufacturing
- Contact us
- …
- 材料测试与制备
- 材料测试
- 催化剂制备
- English
- Who we are
- Products
- Characterisation Services
- Reactor Design & Manufacturing
- Contact us
In situ thermal DRIFTS

Purpose & Applications
In situ thermal DRIFTS is a widely used characterisation technique for investigating catalyst surface processes under controlled heating conditions. It enables real-time monitoring of surface adsorbates, key intermediates, and product evolution, providing direct insight into surface reaction mechanisms and pathways in thermal catalysis. The technique is well suited for a broad range of gas–solid reaction systems, including CO2 hydrogenation, CO hydrogenation, methanation, methanol synthesis, VOC oxidation, and catalytic oxidation, and is widely applied in active-site analysis, catalyst performance evaluation, adsorbed-species identification, intermediate tracking, and dynamic studies of complex catalytic reactions.
Instrument Model
In Situ Plasma DRIFTS Cell (Harrick): Praying Mantis™ High Temperature Reaction Chambers
FTIR Spectrometer (Thermo Fisher Scientific): Nicolet iS50
Mass Spectrometer (Anyeep): GMA6500
Sample Requirements
1 | Sample Type
Suitable for powdered, granular, or supported solid catalysts with adequate diffuse reflectance in the infrared region. Typical samples include metal oxides, zeolites, MOFs, supported metal catalysts, and other porous solid materials.
2 | Sample Amount
A sample amount of 100–500 mg is generally recommended for each measurement. The actual amount may be adjusted depending on the cell size, test mode, and sample packing density. For materials with lower density or weaker reflectance, a larger amount may be required.
3 | Particle Size
Samples should have a relatively uniform particle size. Sieving to 40–80 mesh or grinding to a consistent particle size is generally recommended. Oversized particles may affect sample packing and spectral reproducibility, while excessively fine powders may influence gas transport or lead to sample loss.