4.7 Article

A general way to transform Ti3C2Tx MXene into solvent-free fluids for filler phase applications

期刊

CHEMICAL ENGINEERING JOURNAL
卷 409, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.128082

关键词

Solvent-free fluids; Ti3C2Tx MXene; Filler phases; Gas separation; Composites

资金

  1. Innovation Foundation for Doctor Dissertation of NWPU [CX201963]
  2. National Natural Science Foundation of China [21905228, 41772166, 21706206, 51903208]
  3. Aeronautical Science Foundation of China [2018ZF53065]
  4. Key Industry Chain Innovation Project, Shaanxi Province, China [2017ZDCXL-GY-10-01-02]
  5. China Postdoctoral Science Foundation [2019 M653733]
  6. Fundamental Research Funds for the Central Universities [31020180QD127]
  7. Joint Fund Project in Shaanxi Province of China [2019JLM-22, 2019JLM-4]

向作者/读者索取更多资源

The study introduces a strategy to transform Ti3C2Tx MXene into a novel MX-fluid, which exhibits stable antioxidant ability and improved processability. The MX-fluid shows macroscopic flow behavior at room temperature and addresses dispersion issues when blending with other polymer matrices.
The emerging two-dimensional transition metal carbides (MXenes) have been gradually coming into the limelight due to excellent mechanical properties, electrical conductivity performance and versatile surface chemistry. However, the oxidation instability and poor processability of MXenes impede further scalable applications. Toward this end, we have for the first time proposed a general and facile strategy to transform Ti3C2Tx MXene into a novel class of homogenous, stable solvent-free liquids (MX-fluid) with core-corona-canopy structure via covalent linkage surface engineering strategy. The as-prepared MX-liquid exhibited rather stable antioxidant ability after setting for 540 days. Moreover, the MX-fluid presented macroscopic flow behaviors at room temperature, remarkably improving processability and showing extensive potential in addressing the daunting dispersion issue when blending the Ti3C2Tx with other polymer matrixes. Furthermore, the generality of constructing solvent-free MXene fluids using covalent corona-canopy linkage strategy was verified. As two proof-ofconcept demonstrations, the MX-fluid was first utilized as a filler phase of mixed matrix membranes (MMMs). The MX-fluid exhibited greatly enhanced CO2 uptake compared with that of N-2, which was also confirmed by molecular simulation. Next, the MX-fluid was incorporated into Pebax-1657 matrix, and improved CO2 selective separation (CO2/N-2 selectivity of 69.2) was obtained, where the CO2 permeability increased by 179.9% compared with pristine Pebax-1657 membrane. Second, the MX-fluid was demonstrated a good reinforcement phase of epoxy-based composites. Remarkably, the rich library of MXenes family and oligomer species provides more convenience for the further optimization of structures of solvent-free MXene liquids for task-specific applications, thus paving new ways to advance the development of novel solvent-free MXene liquids into scale-up and practical applications

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