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dc.contributor.advisorPham, Kim Ngoc-
dc.contributor.advisorMac, Trung Kien-
dc.contributor.advisorNguyen, Huu Tuan-
dc.contributor.advisorDo, Thanh Viet-
dc.contributor.advisorTran, Dang Thanh-
dc.contributor.advisorPham, Van Vinh-
dc.contributor.advisorPhan, Bach Thang-
dc.contributor.advisorDuong, Anh Tuan-
dc.contributor.authorDas, Raja-
dc.date.accessioned2021-06-14T04:24:35Z-
dc.date.available2021-06-14T04:24:35Z-
dc.date.issued2021-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S2468217921000113?via%3Dihub#!-
dc.identifier.urihttps://dlib.phenikaa-uni.edu.vn/handle/PNK/1730-
dc.descriptionQ1vi
dc.description.abstractα-Fe2O3 and Fe3O4 nanoplates and nanorices were synthesized by hydrothermal reaction and used for organic pollutant adsorption and removal studies. The effect of size and morphology of α-Fe2O3 and Fe3O4 nanoplates and nanorices on the dye adsorption efficiency were investigated systematically. The adsorption studies showed a good selectivity and high adsorption capacity (~93%) of the α-Fe2O3 nanoplates towards congo red (C.R.) dye, due to the formation of hydrogen bonding between amine group (─ NH2) of C.R. and surface carboxylate group (─ COOH), and adsorbed ─ OH groups of α-Fe2O3 nanoplates. The α-Fe2O3 nanoplates also showed excellent recyclability with negligible loss of the adsorption capacity, owing to their stable morphology and crystal structure. The excellent C.R. adsorption capacity of the α-Fe2O3 nanoplates was further confirmed by conducting experiments with a solution containing a mixture of dyes. Our findings indicate that the synthesized α-Fe2O3 nanoplates have a great potential in removing industrial waste, such as C.R. from polluted water.vi
dc.language.isoenvi
dc.publisherJournal of Science: Advanced Materials and Devicesvi
dc.subjectNanoplatesvi
dc.subjectNanoricesvi
dc.subjectHydrothermalvi
dc.subjectSelective adsorptionvi
dc.titleExcellent organic dye adsorption capacity and recyclability of hydrothermally synthesized α-Fe2O3 nanoplates and nanoricesvi
dc.typeArticlevi
dc.typeWorking Papervi
eperson.identifier.doihttps://doi.org/10.1016/j.jsamd.2021.02.006-
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