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1 ng from the hydride generator as well as the atomizer.
2 of samples were directly dispensed into the atomizer.
3 tion of arsane in the optical arm of the DBD atomizer.
4 o a standard miniature diffusion flame (MDF) atomizer.
5 of that of the externally heated quartz tube atomizer.
6 plied at will) and further injected into the atomizer.
7 always employed a separate light source and atomizer.
8 contamination was found beneath the chamber atomizer.
9 h encapsulated Dp yields using an ultrasonic atomizer.
10 aerosol generated by a medical nebulizer or atomizer.
11 udy water concentration in gases leaving the atomizer.
12 due to fluctuations of hydride supply to an atomizer, a new design of a gas-liquid separator was imp
14 cal sensitivity of 0.48 s ng (-1) As in both atomizers and limits of detection (LOD) of 0.15 ng mL(-1
15 nts/metals that appeared to originate in the atomizers, and concentrations increased with increasing
16 ults support previous work reporting the SAW atomizer as a fast and inexpensive tool for ultrasound,
17 This study employed a system hyphenating the atomizer (ATM), differential mobility analyzer (DMA), an
20 mized to receive intranasal mometasone in an atomizer for 12 weeks (1 application per nostril, once p
21 ort the use of a surface acoustic wave (SAW) atomizer for fast sample handling in matrix-assisted las
23 The high fraction of Bi deposited in the atomizers indicates significant reactivity of free Bi at
25 ser wave mixing in a common graphite furnace atomizer is presented as a zeptomole-level, sub-Doppler,
26 to that of a multiple microflame quartz tube atomizer (MMQTA) for atomic absorption spectrometry (AAS
30 nitric acid leachates from deposition in the atomizer on the one hand and quantification of the Bi fr
31 of the Bi fraction transportable outside the atomizer on the other, were in excellent agreement, prov
32 cal method and those of the graphite furnace atomizer, one can obtain both excellent spectral resolut
34 human influenza virus (H1N1), and HSV1 from atomizer-produced droplet-aerosols were each fully destr
36 mpared to that of a conventional quartz tube atomizer (QTA) for atomic absorption spectrometry (AAS).
37 te atoms in an externally heated quartz tube atomizer (QTA) were investigated employing selected ion
39 ported beyond the confines of the DBD or QTA atomizers, quantified by inductively coupled plasma mass
41 in acidic leachates of the interiors of both atomizers, representing the fraction retained on their s
42 00 ppb) ions were measured in the humic acid atomizer solutions compared to the other organics that c
43 l method developed for nasal delivery via an atomizer spray mist to the nostrils (dose estimated 1.0
45 oratory, Argonne, IL, U.S.A., 1987) using an atomizer system on December 3, 2009 after chemical separ
46 lfactory epithelium using a refillable nasal atomizer that deposits mist onto the olfactory neuro-epi
47 viruses and virucides in a fine-mist bottle atomizer to mimic the generation of oral droplet-aerosol
48 Modification of the inner surface of the DBD atomizer using dimethyldichlorsilane (DMDCS) was essenti
50 a planar dielectric barrier discharge (DBD) atomizer was investigated using a variety of probes, inc
51 ar quartz dielectric barrier discharge (DBD) atomizer was optimized and the performance of this devic
52 ar quartz dielectric barrier discharge (DBD) atomizer was optimized, and its performance was compared
54 Se) on Bi response by AAS using DBD and QTA atomizers was investigated, with the former atomizer pro