Decomposition of carboxymethyl cellulose based on nano-knife principle.

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ID: 3597
2019
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Abstract
The traditional degradation of organic pollutants is based on the sacrifice of chemical or biological reagents. In this study, a purely physical technique was developed to break the chemical bonds and consequently decompose macromolecules in aqueous solution. Assisted with a high-speed mechanical blade, refined quartz sand grains with particularly sharp nano-scale edges can act as 'nano-knives', which are able to cut the long chain of carboxymethyl cellulose (CMC, as a model molecule). High performance size exclusion chromatography measurements evidenced that the original CMC molecules (41,000 Da) were decomposed into a series of smaller molecules (460, 1000, 2200, 21,000, 27,000 and 31,000 Da). Consequently, the initial viscosity of the CMC solution (2 g/L) rapidly decreased by approximately 50% after 3 min treatment by the nano-knife materials along with the mechanical blade. Fourier transform infrared (FTIR) spectra indicated that the original functional groups were still present and new functional groups were not produced after shearing. The intensity of the main functional group β-1-4-glycosidic bond (wavenumber 1062 cm) was observed to markedly decrease after shearing. These results indicated that the long-chain CMC was cleaved into short-chain CMC. A degradation mechanism was proposed whereby the cutting force generated by the rapid motion of the nano-knives may be responsible for the breakage of β-1-4-glycosidic bonds in the macromolecular cellulose backbone. These results provide support for a potentially more affordable and environment-friendly strategy for physical-based decomposition of recalcitrant organic pollutants from aqueous solution without the need of chemical or biological reagents.
Reference Key
zhou2019decompositionjournal Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Zhou, Qin;Hong, Li;Di Bonito, Marcello;Pan, Gang;
Journal Journal of environmental sciences (China)
Year 2019
DOI
S1001-0742(18)31337-8
URL
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