4.7 Article

Internally cross-linked poly (2,6-dimethyl-1,4-phenylene ether) based anion exchange membrane for recovery of different acids by diffusion dialysis

期刊

CHEMICAL ENGINEERING JOURNAL
卷 414, 期 -, 页码 -

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ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.128776

关键词

Poly (2; 6-dimethyl-1; 4-phenylene ether); Anion exchange membrane; Diffusion dialysis; Acid recovery

资金

  1. DAE, BRNS Mumbai
  2. UGC, New Delhi

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This study introduces a novel anion exchange membrane for acid recovery via diffusion dialysis, showing good water uptake and ion exchange capacity for efficient recovery of acids from Cl-1, NO3, and SO42- ions. The membranes exhibit high proton diffusion coefficients and enhanced separation factor values, leading to efficient recovery efficiencies varying with different acids.
Acid recovery from acidic waste is a critical issue to be focused on nowadays. Chemical approaches for recovery are not commercially viable and energy intensive to save the environment. Here, we report internally crosslinked poly (2,6-dimethyl-1,4-phenylene ether) (PPE) based anion exchange membranes (AEMs) for acid recovery by diffusion dialysis, prepared via quick grafting of N-methyl-4-piperidone using ultrasonication. The prepared AEMs are assessed for their physicochemical parameters and depicted water uptake (WU) and ionexchange capacity (IEC) in the range 22.00%?31.00% and 0.64 meq/g?2.18 meq/g respectively for Cl-1, NO3and SO42- ions. AEMs were investigated for recovery of hydrochloric acid (HCl), nitric acid (HNO3) and sulphuric acid (H2SO4) from simulated effluent based on their proton diffusion coefficient (UH+), separation factor (S) and recovery efficiency (?). These membranes illustrated the proton diffusion coefficient as high as 0.065 m h-1 and enhanced separation factor values up to 132 at 27 ?C. Recovery performance for different acids is corroborated based on unique self-organized membrane structure, studied using AFM phase imaging and cumulative influence of bulk diffusion coefficient, ion-exchange capacity, and hydration radii of Cl-1, NO3- and SO42- ions. The acid recovery efficiency illustrated the trend HCl > HNO3 > H2SO4. The hydrate (?OH) functionality with a nonoverlapping set of lone pairs on oxygen enhances the proton mobility via Grotthuss mechanism inside the membrane matrix and provides a cradle-like pathway for high proton mobility. The results are pronounced for fabricated membranes compared to commercially available standards for acid recovery via diffusion dialysis.

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