Figures & data
FIG. 1. Mobility spectrum for a spray of tetrahexadecylammonium bromide, showing on its right boundary the sharp peak associated to (C16H33)4N+.
![FIG. 1. Mobility spectrum for a spray of tetrahexadecylammonium bromide, showing on its right boundary the sharp peak associated to (C16H33)4N+.](/cms/asset/28a4b601-2797-42c1-8ebb-cbb8154425c9/uast_a_999908_f0001_b.gif)
FIG. 2. Mobility spectra from sprays of (C18H37)4N+Br− (open circles) and (C7H15)4N+Br− ions (filled circles) taken under identical conditions of the DMA. The dominant and most mobile peak in the spray of (C18H37)4N+Br− is (C18H37)4N+.
![FIG. 2. Mobility spectra from sprays of (C18H37)4N+Br− (open circles) and (C7H15)4N+Br− ions (filled circles) taken under identical conditions of the DMA. The dominant and most mobile peak in the spray of (C18H37)4N+Br− is (C18H37)4N+.](/cms/asset/d9ed80c3-df57-4a17-ad2b-4cd18552115f/uast_a_999908_f0002_b.gif)
Table 1 Measured electrical mobilities Z in laboratory air based on the (C7H15)4N+ ion standard
FIG. 3. Mobility spectra after passing the electrospray ions through a charge-reduction chamber containing radioactive Ni-63.
![FIG. 3. Mobility spectra after passing the electrospray ions through a charge-reduction chamber containing radioactive Ni-63.](/cms/asset/6451d65c-7262-4575-a04e-1188807cab5d/uast_a_999908_f0003_b.gif)