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Microplastics (MPs) are ubiquitous and evasive in nature. They can be found in complex agricultural matrices like soil and compost. In the literature, extracting MPs from soil is more prevalent; nonetheless, the same instruments in extraction in soil samples can also be used to assess MPs in compost despite the high levels of organic material. MPs in agricultural environments have recently become a focus of research due to their status as emerging pollutants. However, the lack of standardized instruments and techniques for analysis is a major challenge in assessing MPs. Despite this limitation, this review article identified and suggested some important factors to consider when selecting suitable methods or instruments for MP analysis. This article also categorized instrumental analysis in MP studies as destructive and non-destructive and highlighted the advantages and disadvantages of methods and instruments such as visual inspection, Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy (RS), and Scanning Electron Microscope (SEM). These highlights will provide researchers with a useful guide to help them choose the most appropriate method and instrumentation technique for their MP analytical research. Additionally, the article discusses the combination of two or more of these analytical instruments to improve efficiency. [ABSTRACT FROM AUTHOR]

Impact of Swift Heavy Ion (SHI) irradiation is an effective way to tailor the properties of materials to enhance their applicability toward high-end applications. In the present investigation, hydrothermally synthesized Fe-BTC metal-organic frameworks (MOFs) were irradiated with 197Au8+ ion beam, 100 MeV at fluence range of 1×1011 ions/cm² and 1×1012 ions/cm². Hydrothermally synthesized Fe-BTC MOFs were characterized by X-ray diffractometer, UVVisible spectroscopy, Fourier-transform infrared spectroscopy (FTIR), Scanning electron microscope (SEM), Raman spectroscopy, and Atomic Force Microscopy (AFM). The significant modifications were observed as ion fluence increases, viz. decrease of crystallite size, increase of energy bandgap, reduction in average surface roughness, and the formation of new functional group (C-H) at a higher fluences 1×1012 ions/cm². [ABSTRACT FROM AUTHOR]

We report a multi-instrument characterization of the carbon particles in carbon/polymer/nanodiamond core-shell materials used for high-performance liquid chromatography. These particles are prepared by the carbonization/pyrolysis of poly(divinylbenzene) (PDVB) microspheres. Scanning electron microscopy showed that the particles (4.9 µm initially) decreased in size after air oxidation (to 4.4 µm) and again after carbonization (down to 3.5 µm) but remained highly spherical. Brunauer-Emmett-Teller measurements showed low surface areas initially (as received: 1.6 m2/g, after air oxidation: 2.6 m2/g) but high values after carbonization (445 m2/g). Fourier transform infrared spectroscopy revealed the changes in the functional groups after air oxidation (C = O and C-O stretches appear), carbonization (carbon-oxygen containing moieties disappear), and acid treatment (reintroduction of carbon-oxygen containing moieties). X-ray photoelectron spectroscopy (XPS) and elemental analysis revealed the surface and bulk oxygen contents before and after treatments. By XPS, the atom percent oxygen for the as received, air oxidized, carbonized, and acid treated particles are 8.7, 16.6, 3.7, and 13.8, respectively, and by elemental analysis, the percent oxygen in the materials is 0.6, 8.1, 0.9, 16.9, respectively. A principal components analysis of time-of-flight secondary ion mass spectrometry data identified ions that were enhanced in the different materials, where almost 90% of the variation in the analyzed peak areas was captured by two principle components. X-ray diffraction and Raman spectroscopy suggested that the carbonized PDVB was disordered. Thermogravimetric analysis showed significant differences between the differently treated PDVB microspheres. This work applies directly to a commercial product and the process for preparing it. Copyright © 2015 John Wiley & Sons, Ltd. [ABSTRACT FROM AUTHOR]