Atrazine immobilization on sludge derived biochar and the interactive influence of coexisting Pb(II) or Cr(VI) ions

• Published in: Chemosphere (Oxford) 2015-09, Vol.134, p.438-445
• Main Authors: Zhang, Weihua, Zheng, Juan, Zheng, Pingping, Qiu, Rongliang
• Format: Article
• Language: English
• Subjects: Adsorption; Atrazine; Atrazine - chemistry; Atrazine - isolation & purification; Biochar; Charcoal - chemistry; Chromium; Chromium - chemistry; H-bond; Immobilization; Interactive; Kinetics; Lead; Lead - chemistry; Mathematical analysis; Metal ions; Sewage - chemistry; Sludge; Sorption; Water Pollutants, Chemical - chemistry; Water Pollutants, Chemical - isolation & purification
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2015.05.011

[Display omitted] •The sludge derived biochar is an excellent sorbent to immobilize atrazine in water.•400°C 2h is the optimal pyrolysis conditions.•Atrazine sorption may mainly involve site-specific process, i.e., H-bonding.•The coexisting ions significantly suppress the atrazine immobilization on SDBC.•Atrazine does not affect the metal ion immobilization. Sludge derived biochars (SDBCs) may have the potential to simultaneously remove heavy metals and organic contaminants in relation to their various active sorption sites for both metal ions and organic compounds. SDBCs have been proven to provide a considerable capacity for immobilizing Pb(II) and Cr(VI) ions in solution, and in this study their ability to sorb atrazine, in addition to their corresponding interactive influences with coexisting metal ions, is extensively investigated. The results indicate that all atrazine adsorption isotherms fit well with the Freundlich equation, and the greatest value of 16.8mgg−1 sorption capacity occurred with SDBCs pyrolyzed at 400°C for 2h. The slow sorption kinetics fit well with the Lagergren’s 2nd order reaction, and depend upon the initial atrazine concentration, indicating the significance of a site-specific process. The ionic strength-dependence of the atrazine adsorption behavior further consolidates the involvement of the mechanism of the H-bond with hydroxyl groups on SDBC. However, when Pb(II)/Cr(VI) metal ions coexist in solution, they substantially suppress atrazine adsorption, probably because the inner complex between the hydroxyl groups on SDBCs and Pb(II)/Cr(III) ions intrude the weak H-bond with atrazine. As a result, metal adsorption was found to be unaffected by the coexisting atrazine. Therefore, although SDBC is applicable for atrazine removal/immobilization in most of environmentally relevant conditions, a two-step process may be required if heavy metal ions coexist.