AI Article Synopsis

  • A new wood veneer-based composite featuring Pt-loaded NiFe-LDH nanosheets is developed to effectively remove gaseous formaldehyde using a low-energy process.
  • The NiFe-LDH nanosheets capture formaldehyde through their hydroxyl groups, while Pt nanoparticles enhance the reaction to convert formaldehyde into CO and water.
  • Tested in a dark environment at room temperature, this composite successfully degrades nearly all formaldehyde within 30 minutes and retains over 97% efficiency after 10 cycles, making it a promising option for indoor air purification and decorative use.

Article Abstract

Traditional methods of removing gaseous formaldehyde are often associated with high energy consumption and secondary pollution. In this study, a new wood veneer-based composite decorated with Pt-loaded NiFe-LDH nanosheets is successfully developed by a hydrothermal reaction and impregnation-chemical reduction. NiFe-LDH nanosheets as an adsorbent can capture formaldehyde molecules through their abundant hydroxyl groups. Pt nanoparticles as catalytic centers are evenly distributed on the surface of NiFe-LDH to excite the O atoms linked to NiFe-LDH and absorbed oxygen, which will further attack the absorbed formaldehyde molecules to generate CO and HO. And the wood veneer not only increases the active area of the catalyst by endowing it with good dispersion but also provides convenient channels for reactants and products. In a simulated dark environment at room temperature, this synthetic wood veneer-based composite exhibits admirable catalytic activity, which can effectively degrade almost all gaseous formaldehyde with the initial concentration of 0.2 mg m in 30 min and maintain a high catalytic activity of ≥97% after 10 cycles. This paper presents a feasible strategy for synthesizing an energy-efficient and ecofriendly wood veneer-based composite for efficient gaseous formaldehyde degradation at room temperature, which may play an important role in indoor air purification as a promising decorative material.

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http://dx.doi.org/10.1021/acsami.0c09016DOI Listing

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