TY - JOUR
T1 - Pd-Co bimetallic nanoparticles modified α-FeOOH nanorod for the catalytic reduction of organic pollutants
AU - Shanmugaraj, Krishnamoorthy
AU - Mangalaraja, Ramalinga Viswanathan
AU - Manikandan, Velu
AU - Campos, Cristian H.
AU - Packiaraj, S.
AU - Aepuru, Radhamanohar
AU - Noé Díaz de León, J.
AU - Sathish, Manda
AU - Song, Kwang Soup
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/6
Y1 - 2024/6
N2 - The development of most effective reduction catalysts is an essential for promoting the sustainability by minimizing the waste and safeguard the environment. Herein, we prepared palladium-cobalt bimetallic nanoparticles modified on goethite nanorods (PdCo/α-FeOOH) as a catalyst for the catalytic degradation of various organic pollutants under mild reaction conditions. The structure and morphology of synthesized catalysts were tested by XRD, FT-IR, BET, SEM, TEM, HR-TEM and XPS techniques. The ultra-small PdCo bimetallic NPs (2.95 ± 0.5 nm) synthesized onto the surface of α-FeOOH nanorod were confirmed by HR-TEM analysis. The prepared catalysts were played an important role in the reduction of toxic nitrocompounds such as (4-nitrophenol (4-NP), 4-nitroaniline (4-NA), 4-(4-nitrophenyl)morpholine (4-NM) and 4-(2-fluoro-4-nitrophenyl)morpholine (4-FNM)) and rhodamine B (RhB) dye. The PdCo/α-FeOOH nanocatalyst displayed a greater rate constant (∼1.5 min and kapp = 2.631 min−1) compared to their respective mono-metallic counterparts (Pd/α-FeOOH and Co/α-FeOOH). The reusability results indicated that >97 % of conversion for 4-NP, and RhB dye over 10 consecutive reaction cycles in the batch method. Furthermore, the continuous flow reactor with PdCo/α-FeOOH catalyst was constructed, and it showed the ability to eliminate > 99 % of both 4-NP and RhB dye and maintained a degradation rate of >98 % for 20 consecutive recycles. The superior catalytic activity of the PdCo/α-FeOOH catalyst compared to other mono-metallic catalysts could be attributed to their particle size and synergistic effect. This study has the potential to facilitate the utilization of the synthesized bimetallic nanostructure in a wider range of other wastewater treatments.
AB - The development of most effective reduction catalysts is an essential for promoting the sustainability by minimizing the waste and safeguard the environment. Herein, we prepared palladium-cobalt bimetallic nanoparticles modified on goethite nanorods (PdCo/α-FeOOH) as a catalyst for the catalytic degradation of various organic pollutants under mild reaction conditions. The structure and morphology of synthesized catalysts were tested by XRD, FT-IR, BET, SEM, TEM, HR-TEM and XPS techniques. The ultra-small PdCo bimetallic NPs (2.95 ± 0.5 nm) synthesized onto the surface of α-FeOOH nanorod were confirmed by HR-TEM analysis. The prepared catalysts were played an important role in the reduction of toxic nitrocompounds such as (4-nitrophenol (4-NP), 4-nitroaniline (4-NA), 4-(4-nitrophenyl)morpholine (4-NM) and 4-(2-fluoro-4-nitrophenyl)morpholine (4-FNM)) and rhodamine B (RhB) dye. The PdCo/α-FeOOH nanocatalyst displayed a greater rate constant (∼1.5 min and kapp = 2.631 min−1) compared to their respective mono-metallic counterparts (Pd/α-FeOOH and Co/α-FeOOH). The reusability results indicated that >97 % of conversion for 4-NP, and RhB dye over 10 consecutive reaction cycles in the batch method. Furthermore, the continuous flow reactor with PdCo/α-FeOOH catalyst was constructed, and it showed the ability to eliminate > 99 % of both 4-NP and RhB dye and maintained a degradation rate of >98 % for 20 consecutive recycles. The superior catalytic activity of the PdCo/α-FeOOH catalyst compared to other mono-metallic catalysts could be attributed to their particle size and synergistic effect. This study has the potential to facilitate the utilization of the synthesized bimetallic nanostructure in a wider range of other wastewater treatments.
KW - 4-Nitrophenol
KW - Bimetallic nanoparticles
KW - Catalytic reduction
KW - Continuous flow reactor
KW - Rhodamine B
KW - Synergistic effect
UR - http://www.scopus.com/inward/record.url?scp=85192782281&partnerID=8YFLogxK
U2 - 10.1016/j.jece.2024.112942
DO - 10.1016/j.jece.2024.112942
M3 - Article
AN - SCOPUS:85192782281
SN - 2213-3437
VL - 12
JO - Journal of Environmental Chemical Engineering
JF - Journal of Environmental Chemical Engineering
IS - 3
M1 - 112942
ER -