Details

Autor(en) / Beteiligte

• Jeong, Jae‐Min
• Jin, Se Bin
• Park, Hong Jun
• Park, Seung Hwa
• Jeon, Hyeonyeol
• Suh, Hoyoung
• Park, Yong‐Ju
• Seo, Donghyuk
• Hwang, Sung Yeon
• Kim, Do Hyun
• Choi, Bong Gill

Titel

Large‐Scale Fast Fluid Dynamic Processes for the Syntheses of 2D Nanohybrids of Metal Nanoparticle‐Deposited Boron Nitride Nanosheet and Their Glycolysis of Poly(ethylene terephthalate)

Ist Teil von

• Advanced materials interfaces, 2020-08, Vol.7 (16), p.n/a

Ort / Verlag

Weinheim: John Wiley & Sons, Inc

Erscheinungsjahr

2020

Quelle

Wiley-Blackwell Journals

Beschreibungen/Notizen

• Owing to the unique mass and heat transfer, fluidic‐flow control systems or reactors can potentially provide advantages for organic and inorganic syntheses compared to the static reactors. In this study, it is demonstrated that a fluid dynamic reactor based on Taylor–Couette (T–C) flow provides high‐throughput processes for the exfoliation of hexagonal boron nitride (hBN), syntheses of metal‐nanoparticle‐(NP)‐deposited hBN nanohybrids, and their glycolysis reactions of poly(ethylene terephthalate) (PET). The mechanical shear force and dynamic mixing behavior of the T–C flow lead to a stable colloidal suspension of exfoliated hBN sheets with a high exfoliation yield of 77.9% and high production rate of 0.48 g h−1. A fast synthesis of metal NPs (Pd, Pt, Ag, and RuO2 NPs) onto the hBN surface is achieved by using the controlled T–C flow within only 2 min owing to the efficient mass and heat transfer of the T–C flow. The T–C flow considerably reduces the reaction time (30 min) and temperature (100 °C) for the Pd/hBN‐catalyst‐based glycolysis reaction of PET to bis(2‐hydroxyethyl) terephthalate compared to those of the conventional static reaction that is performed above 200 °C for 120 min. Fluid dynamic process is developed for the exfoliation of hexagonal boron nitride (hBN) and the synthesis of nanoparticle‐deposited hBN nanohybrids. The nanohybrid‐catalyzed glycolysis reaction for poly(ethylene terephthalate) degradation using fluid dynamic reactor results in superior catalytic performances compared to those of conventional hydrothermal and round flask‐reactions.