期刊论文详细信息
Materials
Facile Fabrication of Novel NiFe2O4@Carbon Composites for Enhanced Adsorption of Emergent Antibiotics
Long Giang Bach1  Thi Cam Quyen Ngo1  Van Tan Lam1 
[1] Institute of Environmental Technology and Sustainable Development, Nguyen Tat Thanh University, Ho Chi Minh City 700000, Vietnam;
关键词: wastewater treatment;    antibiotic pollutants;    metal-organic frameworks;    magnetic composites;    response surface methodology;   
DOI  :  10.3390/ma14216710
来源: DOAJ
【 摘 要 】

Water purification is becoming one of the most pertinent environmental issues throughout the world. Among common types of water pollution involving heavy metals, pharmaceutical drugs, textile dyes, personal care products, and other persistent organic pollutants, the pollution of antibiotic drugs is increasingly emerging due to their adverse effects on microorganisms, aquatic animals, and human health. Therefore, the treatment of such contaminants is very necessary to reduce the concentration of antibiotic pollutants to permissible levels prior to discharge. Herein, we report the use of NiFe2O4@C composites from a bimetallic-based metal-organic framework Ni-MIL-88B(Fe) for removal of ciprofloxacin (CFX) and tetracycline (TCC). The effect of production temperatures (600–900 °C), solution pH (2–10), NiFe2O4@C dose (0.05–0.2 g/L), concentration of antibiotics (10–60 mg/L), and uptake time (0–480 min) was investigated systematically. Response surface methodology and central composite design were applied for quadratic models to discover optimum conditions of antibiotic adsorption. With high coefficients of determination (R2 = 0.9640–0.9713), the proposed models were significant statistically. Under proposed optimum conditions, the adsorption capacity for CFX and TCC were found at 256.244, and 105.38 mg/g, respectively. Recyclability study was employed and found that NiFe2O4@C-900 could be reused for up to three cycles, offering the potential of this composite as a good adsorbent for removal of emergent antibiotics.

【 授权许可】

Unknown   

  文献评价指标  
  下载次数:0次 浏览次数:0次