4.8 Article

Targeting Metal Impurities for the Detection and Quantification of Carbon Black Particles in Water via spICP-MS

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 56, 期 19, 页码 13719-13727

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c03130

关键词

graphitic nanoparticles; metal tracers; mass spectrometry; single particle ICP-MS; detection limits; carbonaceous nanomaterial analysis

资金

  1. National Science Foundation [EEC-144950, ECCS-1542160]
  2. Nanosystems Engineering Research Center on Nanotechnology-Enabled Water Treatment
  3. NNCI: Nanotechnology Collaborative Infrastructure Southwest (NCI-SW) [ECCS- 1542160]
  4. Endowed Research Professorship and the Academy of Applied Science/Army Eductional Outreach Program (AEOP)
  5. LEER programs of the University of Texas System
  6. University of Texas System FY 2018 STARs retention award [201-1224]
  7. Consejo Nacional de Ciencia y Tecnologia , Mexico [905265]

向作者/读者索取更多资源

This study aimed to establish a quantification method for carbon black (CB) in water using trace metal impurities as analytical tracers, with La chosen as the tracer based on measured concentration, low detection limits, and lack of polyatomic interferences.
Carbon black (CB) is a nanomaterial with numerous industrial applications and high potential for integration into nano-enabled water treatment devices. However, few analytical techniques are capable of measuring CB in water at environmentally relevant concentrations. Therefore, we intended to establish a quantification method for CB with lower detection limits through utilization of trace metal impurities as analytical tracers. Various metal impurities were investigated in six commercial CB materials, and the Monarch 1000 CB was chosen as a model for further testing. The La impurity was chosen as a tracer for spICP-MS analysis based on measured concentration, low detection limits, and lack of polyatomic interferences. CB stability in water and adhesion to the spICP-MS introduction system presented a challenge that was mitigated by the addition of a nonionic surfactant to the matrix. Following optimization, the limit of detection (64 mu g/L) and quantification (122 mu g/L) for Monarch 1000 CB demonstrated the applicability of this approach to samples expected to contain trace amounts of CB. When compared against gravimetric analysis and UV-visible absorption spectroscopy, spICP-MS quantification exhibited similar sensitivity but with the ability to detect concentrations an order of magnitude lower. Method detection and sensitivity was unaffected when dissolved La was spiked into CB samples at environmentally relevant concentrations. Additionally, a more complex synthetic matrix representative of drinking water caused no appreciable impact to CB quantification. In comparison to existing quantification techniques, this method has achieved competitive sensitivity, a wide working range for quantification, and high selectivity for tracing possible release of CB materials with known metal contents.

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