4.7 Article

Ambient NO2 adsorption removal by Mg-Al layered double hydroxides and derived mixed metal oxides

Journal

JOURNAL OF CLEANER PRODUCTION
Volume 313, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jclepro.2021.127956

Keywords

Ambient NO2 adsorption; Layered double hydroxides; Mixed metal oxides; Acid-base interaction; High-capacity adsorbents

Funding

  1. National Natural Science Foundation of China [21706224]
  2. Science and Technology Innovation Commission of Shenzhen Municipality [JCYJ20180307123906004, JCYJ20190808181003717]
  3. Research Grants Council of Hong Kong [CityU 21301817, 11215518, PolyU 15222020]
  4. City University of Hong Kong [CityU 11306419, 11308420, CityU 9667217]

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NO2 is a potent air pollutant that can be captured directly from the atmosphere by selective adsorption on porous materials. The study reports the rational development and demonstration of Mg-Al layered double hydroxides and their derived mixed metal oxides as high-capacity adsorbents. By boosting the densities of accessible basic sites, the highest NO2 adsorption capacity was achieved, offering promising, durable, and scalable adsorbents for ambient NO2 removal.
NO2 is a potent air pollutant because of its deleterious effects on human beings and other organisms. The state-ofthe-art catalysis-based deNOx techniques (e.g., selective catalytic/non-catalytic reduction) are incapable of ambient NO2 abatement due to their low efficiency at temperatures below 300 degrees C. It is thus conceivable to directly capture NO2 from the atmosphere by selective adsorption on porous materials. This work reports the rational development and demonstration of the Mg-Al layered double hydroxides (LDHs) and their derived mixed metal oxides (MMO), using environmentally benign solvents, as high-capacity adsorbents for ambient NO2 abatement. By boosting the densities of accessible basic sites using layer delamination strategies, the highest NO2 adsorption capacity of 8.52 mmol/g was achieved by the delaminated LDH material (LDH-AM), which was substantially higher than other popular and robust adsorbents, such as zeolites (0.36-3 mmol/g) and carbonbased adsorbents (2-6 mmol/g). Using Fourier transform infrared spectroscopy and powder X-ray diffraction, it was revealed that NO2 adsorption occurs on the surface M-OH basic sites and within the layers by simultaneously replacing the interlayer CO32- ions of LDH. This work affords not only promising, durable, and scalable adsorbents for ambient NO2 removal but also a strategy to develop adsorbents with high density of basic sites for capture of other pollutant acid gases from the environment.

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