4.7 Article

Facilely synthesized cobalt doped hydroxyapatite as hydroxyl promoted peroxymonosulfate activator for degradation of Rhodamine B

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 384, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2019.121447

Keywords

Co-hydroxyapatite; Cobalt-based catalyst; PMS; Co-catalytic; RhB

Funding

  1. National Natural Science Foundation of China [U1501231, 21976042]
  2. Guangdong Provincial Key Laboratory of radioactive contamination control and resources [2017B030314182]
  3. Guangdong Key Laboratory of Environmental Catalysis and Health Risk Control [2018B030322014]
  4. Science and Technology Research Programs of Guangzhou City [201804020072]
  5. Hongkong Scholarship [XJ2016037]
  6. University's 2017 training program for young top-notch personnels [BJ201706]
  7. Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme (2018)

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Hydroxyapatite (HAP) is a promising supporter of catalyst due to its potential in immobilizing metals stably. HAP supported cobalt-based catalyst (Co-HAP) was synthesized via a facile ion exchange-calcination method to reduce the Co leaching. The synthesized Co-HAP was characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscope (TEM), Brunauer-Emmett-Teller (BET) analysis and X-ray photoelectron spectroscopy (XPS). Cobalt ions were incorporated into HAP structure and Co3O4 on HAP surface. Co-HAP showed satisfactory performance in peroxymonosulfate (PMS) activation for eliminating Rhodamine B (RIB) in aqueous solution. Co-HAP even revealed a better activity than that of CoFe2O4. center dot OH, SO4 center dot- and O-1(2) were all involved in RhB degradation and O-1(2) played a leading role. High content of surface oxygen groups could be found on Co-HAP after RhB degradation, which might be resulted from the high amounts of hydroxyl groups. The presence of hydroxyl groups performed the co-catalytic activity of PMS activation in Co-HAP/PMS system.

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