The removal of Cr ions from contaminated wastewater is of great urgency from both environmental protection and resource utilization perspectives. Herein, we developed a superstable mineralization method to immobilize Cr ions from wastewater using CuO as a stabilizer, leading to the formation of a CuCr layered double hydroxide (denoted as CuCr-LDH). CuO showed a superior Cr removal performance with a removal efficiency of 97.97% and a maximum adsorption capacity of 207.6 mg/g in a 13000 mg/L Cr ion solution. and X-ray absorption fine structure characterizations were carried out to elucidate the superstable mineralization mechanism. Two reaction pathways were proposed including coprecipitation-dissolution and topological transformation. The mineralized product of CuCr-LDH can be reused for the efficient removal of organic dyes, and the adsorption capacities were up to 248.0 mg/g for Congo red and 240.1 mg/g for Evans blue, respectively. Moreover, CuCr-LDH exhibited a good performance for photocatalytic CO reduction to syngas (H/CO = 2.66) with evolution rates of 54.03 μmol/g·h for CO and of 143.94 μmol/g·h for H under λ > 400 nm, respectively. More encouragingly, the actual tanning leather Cr wastewater treated by CuO showed that Cr can reduce from 3438 to 0.06 mg/L, which was much below discharge standards (1.5 mg/L). This work provides a new approach to the mineralization of Cr ions through the "salt-oxide" route, and the findings reported herein may guide the future design of highly efficient mineralization agents for heavy metals.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.2c10298DOI Listing

Publication Analysis

Top Keywords

superstable mineralization
12
wastewater cuo
8
mineralization
5
insights superstable
4
mineralization chromiumiii
4
wastewater
4
chromiumiii wastewater
4
cuo
4
removal
4
cuo removal
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!