The reactions between amines and carbon dioxide (CO2) are among the most commonly used and important carbon fixation reactions at present. Microdroplets generated by electrospray ionization (ESI) have been proved to increase the conversion ratio (R C) of amines. In this work, we confirmed that the presence of ammonium bicarbonate (NH4HCO3) in ESI microdroplets significantly increased the R C of amines. The R C went up remarkably with the increase in the concentration of NH4HCO3 from 0.5 to 20 mM. The R C of N,N-dibutyl-1,3-propanediamine (DBPA) reached 93.7% under 20 mM NH4HCO3, which was significantly higher than previous reports. The rise in R C became insignificant when the concentration of NH4HCO3 was increased beyond 20 mM. Further investigations were made on the mechanism of the phenomenon. According to the results, it was suggested that NH4HCO3 decomposed into CO2 and formed microbubbles within the microdroplets of ESI. The microbubbles acted as direct internal CO2 sources. The conversion reactions occurred at the liquid–gas interface. The formation of CO2 microbubbles remarkably increased the total area of the interface, thus promoting the conversion reactions. 13C-labeled experiments confirmed that NH4HCO3 acted as an internal CO2 source. Factors that influenced the R C of the reaction were optimized. Pure water was proved to be the optimal solvent. Lower temperature of the mass spectrometer’s entrance capillary was beneficial to the stabilization of the product carbamic acids. The sample flow rate of ESI was crucial to the R C. It determined the initial sizes of the microdroplet. Lower flow rates ensured higher R C of amines. The present work implied that NH4HCO3 could be a superior medium for CO2 capture and utilization. It might offer an alternative choice for future CO2 conversion research studies. In addition, our study also provided evidence that NH4HCO3 decomposed and generated microbubbles in the droplets during ESI. Attention should be paid to this when using NH4HCO3 as an additive in mass spectrometry-based analysis.

Regulation of protein's charge state in electrospray is of great importance to the analysis of proteins. Different methods have been developed so far to increase the charge state of proteins. In this work, we investigated the influence of different anions on the charge state of proteins. Both strong acid anions and weak acid anions were taken into consideration. The results showed that the presence of 5 mM strong acid anions in acidic solutions could significantly increase the charge state of proteins. In comparison, weak acid anions with the same concentration in solution had little impact on the charge state of proteins. The species of the cations in the samples had very limited influence on the charge state. The presence of a certain amount of acid in sample solution was critical to the effect of strong acid anions. Almost no increase of the charge state was observed when no acid was added to the samples. However, remarkable increase of the charge state of myoglobin (Mb) was observed when 0.001% (v/v) acetic acid (HAc) was added to the sample together with 5 mM sodium chloride (NaCl). A higher concentration of acid in samples would further enhance the effect of strong acid anions on the increase of the charge state. Further investigations into the mechanism revealed that the effect of the strong acid anions on the charge state of proteins was based on the unfolding of the protein molecules during electrospray ionization (ESI). The interactions among H + , anions, and protein molecules were so strong that it caused the unfolding of protein molecules and resulted in the increasing of proteins' charge states. The key factor that made strong acid anions and weak acid anions different in the results was the hydrolysis of the weak acid anions in acidic solutions. The present work furthers our understanding about electrospray, as well as the regulation of protein charge state. The presence of strong acid anions in acidic solutions can significantly influence the charge state of proteins in electrospray. Attention should be paid to this when regulating the charge state of proteins.

Polycyclic aromatic hydrocarbons (PAHs) are a class of low-polarity environmental contaminants that have severe carcinogenic effects and have drawn worldwide attention. However, there remains a challenge for current mass spectrometric...

Rationale: Generally, amines form protonated cations ([M + H] + ) in positive polarity during electrospray ionization (ESI). However, it was found that large conjugated amines (LCAs) had binary ionization choices of generating either radical cations (M •+ ) or [M + H] + during ESI. Investigation on the mechanism would further our understanding of ESI. Methods: In this work, the binary ionization behavior of LCAs was reported and studied. Internal factors (functional groups and sizes of conjugated systems) and external factors (solvent type, flow rate, and electrode position) were systematically investigated and discussed. Results: For the internal factors, electron-donating groups and large conjugated structures of LCAs were conducive to the generation of M •+ . For the external factors, aprotic solvent, higher flow rate, and shorter distance from the electrode to the spray cone facilitated the formation of M •+ but hampered the generation of [M + H] + . Conclusion: The present study illustrated that the formations of M •+ and [M + H] +