Abstract

Cadmium pigments are a group of inorganic pigments used in consumer products. The aggregation behavior and photo-dissolution process of cadmium pigment nanoparticles in aquatic systems control their environmental fate, which is largely unknown. Herein, we investigated the influence of dissolved organic matter (DOM) on the aggregation behavior and photo-dissolution process of CdS nanoparticles in aquatic systems. Bare CdS nanoparticles are prone to aggregation in both NaCl and CaCl2 solutions. DOM can remarkably increase the colloidal stability of CdS nanoparticles owing to the steric hindrance and enhanced electrostatic repulsion. With 10 mg/L Suwannee River natural organic matter (SRNOM), the colloidal stability of CdS nanoparticles is significantly enhanced in NaCl solutions (i.e., the critical coagulation concentration, CCCNa, is 707.2 mM). Suwannee River humic acid (SRHA) has a stronger stabilization effect than SRNOM due to its higher molecular weight and aromaticity. The Ca2+ cations can induce charge neutralization and structural compacting of DOM corona, efficiently reducing the colloidal stability of CdS nanoparticles. The CCCCa is 10.8 mM and 14.9 mM with 10 mg/L SRNOM and SRHA, respectively. Upon solar irradiation, the presence of a low concentration of SRNOM (3 mg/L) can enhance the photo-dissolution of CdS nanoparticles and the consequent Cd2+ leaching. This is caused by the facilitated electron transfer from CdS nanoparticles to O2 induced by SRNOM corona, leading to better electron-hole separation. However, a high concentration of SRNOM inhibited the photo-dissolution of CdS nanoparticles due to the strong inner filter effect and the scavenging of phototransients. The colloidal stability of SRNOM-coated CdS nanoparticles increases in NaCl but decreases in CaCl2 solutions after irradiation owing to the oxidation of SRNOM corona. Our results highlight the decisive role of DOM in the environmental fate of cadmium pigments.

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