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Porous alginate hydrogel beads with spatially separated acidic and basic moieties for selective adsorption of dyes

Journal of Cleaner Production, ISSN: 0959-6526, Vol: 451, Page: 141985
2024
  • 14
    Citations
  • 0
    Usage
  • 16
    Captures
  • 1
    Mentions
  • 0
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    14
  • Captures
    16
  • Mentions
    1
    • News Mentions
      1
      • News
        1

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Findings from Heilongjiang University in the Area of Environment and Sustainability Research Described (Porous Alginate Hydrogel Beads With Spatially Separated Acidic and Basic Moieties for Selective Adsorption of Dyes)

2024 JUN 12 (NewsRx) -- By a News Reporter-Staff News Editor at Ecology Daily News -- Research findings on Environment - Environment and Sustainability Research

Article Description

Currently, obtaining an efficient dual-functional adsorbent for the treatment of complex wastewater containing multiple coexisting anionic and cationic pollutants remains a challenge. In this study, sulfonated waste tire rubber powder (S-WTR) was employed as the cationic binding site, while polyethyleneimine crosslinked with sodium alginate (PS) served as the anionic binding site. Finally, nanoporous CaCO 3 was introduced for pore formation, resulting in the development of S-WTR @ PS sodium alginate composite porous hydrogel beads (S-WTR@PS/SA) with distinct adsorption site spatial separation characteristics. S-WTR@PS/SA enable rapid surface charge conversion based on pH, facilitating the selective removal of dyes, and exhibit outstanding adsorption performance. At pH = 9, it achieves maximum adsorption capacities of 480.7 mg/g for Methylene Blue (MB) and 1256.28 mg/g for Crystal Violet (CV), while at pH = 2, it reaches respective maximum adsorption capacities of 840.34 mg/g for Acid Red-73 (AR-73) and 869.86 mg/g for Acid Yellow-17 (AY-17). Recycling experiments indicated that S-WTR@PS/SA could be reused more than five times, confirming its robust reusability and structural stability. Combining characterization methods such as FT-IR and XPS, the adsorption mechanisms of S-WTR@PS/SA were explored. The primary mechanism involves electrostatic interactions, complemented by hydrogen bonding and π-π stacking interactions. Ultimately, fixed-bed adsorption experiments were carried out to evaluate the practical application capability of S-WTR@PS/SA. It was demonstrated that S-WTR@PS/SA maintained its structural integrity and excellent adsorption capacity during the continuous adsorption of various dyes, further confirming its potential for industrial applications.

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