Highly efficient and irreversible removal of cadmium through the formation of a solid solution

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Highly efficient and irreversible removal of cadmium through the formation of a solid solution. / Wang, Chen; Yin, Hui; Bi, Lei; Su, Jing; Zhang, Meiyi; Lyu, Tao; Cooper, Mick; Pan, Gang.

In: Journal of Hazardous Materials, Vol. 384, 121461, 2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Wang, C, Yin, H, Bi, L, Su, J, Zhang, M, Lyu, T, Cooper, M & Pan, G 2020, 'Highly efficient and irreversible removal of cadmium through the formation of a solid solution', Journal of Hazardous Materials, vol. 384, 121461. https://doi.org/10.1016/j.jhazmat.2019.121461

APA

Wang, C., Yin, H., Bi, L., Su, J., Zhang, M., Lyu, T., Cooper, M., & Pan, G. (2020). Highly efficient and irreversible removal of cadmium through the formation of a solid solution. Journal of Hazardous Materials, 384, [121461]. https://doi.org/10.1016/j.jhazmat.2019.121461

Vancouver

Wang C, Yin H, Bi L, Su J, Zhang M, Lyu T et al. Highly efficient and irreversible removal of cadmium through the formation of a solid solution. Journal of Hazardous Materials. 2020;384. 121461. https://doi.org/10.1016/j.jhazmat.2019.121461

Author

Wang, Chen ; Yin, Hui ; Bi, Lei ; Su, Jing ; Zhang, Meiyi ; Lyu, Tao ; Cooper, Mick ; Pan, Gang. / Highly efficient and irreversible removal of cadmium through the formation of a solid solution. In: Journal of Hazardous Materials. 2020 ; Vol. 384.

Bibtex

@article{cd700336d0f64ff59d21afac02afd002,
title = "Highly efficient and irreversible removal of cadmium through the formation of a solid solution",
abstract = "Sulfur-containing materials are very attractive for the efficient decontamination of some heavy metals. However, the effective and irreversible removal of Cd2+, coupled with a high uptake efficiency, remains a great challenge due to the relatively low bond dissociation energy of CdS. Herein, we propose a new strategy to overcome this challenge, by the incorporation of Cd2+ into a stable ZnxCd1-xS solid solution, rather than into CdS. This can be realised through the adsorption of Cd2+ by ZnS nanoparticles, which have exhibited a Cd2+ uptake capacity of approximate 400 mg g−1. Through this adsorption mechanism, the Cd2+ concentration in a contaminated solution could effectively be reduced from 50 ppb to <3 ppb, a WHO limit acceptable for drinking water. In addition, ZnS continued to exhibit this noteworthy uptake capacity even in the presence of Cu2+, Pb2+, and Hg2+. ZnS displayed high chemical stability. Particles aged in air for 3 months still retained a> 80% uptake capacity for Cd2+, compared with only 9% uptake capacity for similarly-aged FeS particles. This work reveals a new mechanism for Cd2+ removal with ZnS and establishes a valuable starting point for further studies into the formation of solid solutions for hazardous heavy metal removal applications.",
author = "Chen Wang and Hui Yin and Lei Bi and Jing Su and Meiyi Zhang and Tao Lyu and Mick Cooper and Gang Pan",
year = "2020",
doi = "10.1016/j.jhazmat.2019.121461",
language = "English",
volume = "384",
journal = "Journal of Hazardous Materials",
issn = "0304-3894",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Highly efficient and irreversible removal of cadmium through the formation of a solid solution

AU - Wang, Chen

AU - Yin, Hui

AU - Bi, Lei

AU - Su, Jing

AU - Zhang, Meiyi

AU - Lyu, Tao

AU - Cooper, Mick

AU - Pan, Gang

PY - 2020

Y1 - 2020

N2 - Sulfur-containing materials are very attractive for the efficient decontamination of some heavy metals. However, the effective and irreversible removal of Cd2+, coupled with a high uptake efficiency, remains a great challenge due to the relatively low bond dissociation energy of CdS. Herein, we propose a new strategy to overcome this challenge, by the incorporation of Cd2+ into a stable ZnxCd1-xS solid solution, rather than into CdS. This can be realised through the adsorption of Cd2+ by ZnS nanoparticles, which have exhibited a Cd2+ uptake capacity of approximate 400 mg g−1. Through this adsorption mechanism, the Cd2+ concentration in a contaminated solution could effectively be reduced from 50 ppb to <3 ppb, a WHO limit acceptable for drinking water. In addition, ZnS continued to exhibit this noteworthy uptake capacity even in the presence of Cu2+, Pb2+, and Hg2+. ZnS displayed high chemical stability. Particles aged in air for 3 months still retained a> 80% uptake capacity for Cd2+, compared with only 9% uptake capacity for similarly-aged FeS particles. This work reveals a new mechanism for Cd2+ removal with ZnS and establishes a valuable starting point for further studies into the formation of solid solutions for hazardous heavy metal removal applications.

AB - Sulfur-containing materials are very attractive for the efficient decontamination of some heavy metals. However, the effective and irreversible removal of Cd2+, coupled with a high uptake efficiency, remains a great challenge due to the relatively low bond dissociation energy of CdS. Herein, we propose a new strategy to overcome this challenge, by the incorporation of Cd2+ into a stable ZnxCd1-xS solid solution, rather than into CdS. This can be realised through the adsorption of Cd2+ by ZnS nanoparticles, which have exhibited a Cd2+ uptake capacity of approximate 400 mg g−1. Through this adsorption mechanism, the Cd2+ concentration in a contaminated solution could effectively be reduced from 50 ppb to <3 ppb, a WHO limit acceptable for drinking water. In addition, ZnS continued to exhibit this noteworthy uptake capacity even in the presence of Cu2+, Pb2+, and Hg2+. ZnS displayed high chemical stability. Particles aged in air for 3 months still retained a> 80% uptake capacity for Cd2+, compared with only 9% uptake capacity for similarly-aged FeS particles. This work reveals a new mechanism for Cd2+ removal with ZnS and establishes a valuable starting point for further studies into the formation of solid solutions for hazardous heavy metal removal applications.

U2 - 10.1016/j.jhazmat.2019.121461

DO - 10.1016/j.jhazmat.2019.121461

M3 - Journal article

C2 - 31685320

VL - 384

JO - Journal of Hazardous Materials

JF - Journal of Hazardous Materials

SN - 0304-3894

M1 - 121461

ER -

ID: 229782079