The removal of CrIII 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 Cr3+ 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 Cr3+ removal performance with a removal efficiency of 97.97% and a maximum
adsorption capacity of 207.6 mg/g in a 13000 mg/L Cr3+ ion
solution. In situ and ex situ 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 CO2 reduction to syngas (H2/CO
= 2.66) with evolution rates of 54.03 μmol/g·h for CO and
of 143.94 μmol/g·h for H2 under λ >
400
nm, respectively. More encouragingly, the actual tanning leather Cr3+ wastewater treated by CuO showed that Cr3+ 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 Cr3+ ions through the “salt-oxide” route,
and the findings reported herein may guide the future design of highly
efficient mineralization agents for heavy metals.