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Effect of NH4F treatment on the chromaticity of the Ba2+-doped γ-Ce2S3 red pigment

  • Xin Li
  • Yueming LiEmail author
  • Zhike Li
  • Zhumei Wang
  • Yan Hong
  • Fusheng Song
Article
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Abstract

The Ba2+-doped cerium precursor powder, (Ce, Ba)CO3, was successfully prepared via a co-precipitation reaction method using Ce(NO3)3·6H2O, Ba(NO3)3, and (NH4)2CO3 as raw materials. The above powder was placed in a muffle furnace and calcined at 1000°C for 120 min to obtain the corresponding oxide, (Ce, Ba)O2, subsequently, and the oxide was vulcanized at 850°C for 150 min with CS2 as a sulfur source to obtain the Ba2+-doped γ-Ce2S3 red pigment. The effects of different NH4F concentrations (1.0, 2.5, and 4.0 M) and treatment times (30, 60, 90, and 120 min) on the phase composition and chromaticity of the pigment were studied by scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), X-ray diffractometry (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and CIELAB colorimetry. The SEM and EDS analyses revealed the presence of irregular flaky particles on the pigment surface after the NH4F treatment; the amounts of particles gradually increased with the NH4F concentration. The XRD and Raman spectra confirmed that these particles were CeF3 and CeFS heterophases. Furthermore, the Raman spectra denoted the presence of amorphous carbon. The XPS analysis demonstrated that the NH4F treatment did not change the valence of Ce (Ce3+ for γ-Ce2S3). The chromaticity of a sample reached its maximum (L* = 34.24, a* = 38.19, and b* = 39.95) after it was treated using 2.5 M NH4F for 60 min, indicating that the elimination of amorphous carbon can effectively improve the pigment chromaticity.

Keywords

Ba2+-doped γ-Ce2S3 red pigment NH4F-treated chromaticity 

Notes

Acknowledgments

This work was supported by National Natural Science Foundation of China (No. 51462010), Natural Science Foundation of Jiangxi Province (Nos. 20161BAB206132 and 20171ACB20022), Science and Technology Research Project of Jiangxi Education Department (No. GJJ180715), Jingdezhen City Science and Technology project (2017GYZD019-012), and the Innovation fund of Jingdezhen Ceramic Institute (No. JYC-201803).

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Copyright information

© American Coatings Association 2020

Authors and Affiliations

  1. 1.School of Materials Science and Engineering, Jingdezhen Ceramic Institute, National Light Industry Key Laboratory of Functional Ceramic MaterialsEnergy Storage and Conversion Ceramic Materials Engineering Laboratory of Jiangxi ProvinceJingdezhenPeople’s Republic of China

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