“…As recently reviewed, [12] to establish and improve the quantitative behavior of this technique, a number of different approaches have been recommended, usually through optimization of NMR parameters, such as the rate of MAS, contact time, and recycle delay, so that 13 C nuclei in all carbon functional groups will be equally detected. Once again, readers are encouraged to consult the comprehensive reviews of Cook, [36] Simpson and Simpson, [37] and Conte et al [45] and references therein to obtain a more complete understanding of the recommended procedures to obtain the most possible quantitatively correct solid-state CP-MAS 13 C NMR spectra of natural organic matter. In the works published thus far focusing on OA and their water-soluble fractions, MAS frequencies range from 5 to 10 kHz, contact times are generally between 1 and 5 ms, and recycle delay times range from 1 to 5 s. In order to obtain a quantitatively correct CP-MAS 13 C NMR spectrum of aerosol WSOM, it is advisable to use a MAS rate of 10 kHz for reducing the number and intensity of spinning sidebands, [42] a contact time of 1.0 ms, [40] and a recycle delay of 5 s. [40] Even if the NMR equipment is properly set and spectra manipulation is not userdependent, the CP technique may still underestimate C NMR data also shows evidence that the WSOM from aerosols exhibit the same main carbon functional groups, but their relative abundances are quite different.…”