Abstract. In this study the impact of humidity on heterogeneous nucleation of n-butanol onto hygroscopic and nonabsorbent charged and neutral particles was investigated using a fast expansion chamber and commercial continuous flow type condensation particle counters (CPCs). More specifically, we measured the activation probability of sodium chloride (NaCl) and silver (Ag) nanoparticles by using n-butanol as condensing liquid with the size analyzing nuclei counter (SANC). In addition, the cutoff diameters of regular butanol-based CPCs for both seed materials under different charging states were measured and compared to SANC results. Our findings reveal a strong humidity dependence of NaCl particles in the sub-10 nm size range since the activation of sodium chloride seeds is enhanced with increasing relative humidity. In addition, negatively charged NaCl particles with a diameter below 3.5 nm reveal a charge-enhanced activation. For Ag seeds this humidity and charge dependence was not observed, underlining the importance of molecular interactions between seed and vapor molecules. Consequently, the cutoff diameter of a butanol-based CPC can be reduced significantly by increasing the relative humidity. This finding suggests that cutoff diameters of butanol CPCs under ambient conditions are likely smaller than corresponding cutoff diameters measured under clean (dry) laboratory conditions. At the same time, we caution that the humidity dependence may lead to wrong interpretations if the aerosol composition is not known.

State-of-the-art aerosol nanoparticle techniques all have one feature in common: for analysis they remove the nanoparticles from their original environment. Therefore, physical and chemical properties of the particles might be changed or cannot be measured correctly. To overcome these shortcomings, we apply synchrotron based small angle X-ray scattering (SAXS) as an in-situ measurement technique. Contrasting other aerosol studies using SAXS, we focus on particle concentrations which allow direct comparison to common aerosol nanoparticle analyzers. To this end, we analyze aerosol nanoparticles at ambient pressure and concentrations of slightly above ~10 6 cm −3 . A differential mobility particle sizer (DMPS) is operated in parallel. We find that SAXS enables measurement of the primary particles and the aggregates, whereas the DMPS detects only aggregates. We conclude that in-situ nanoparticle characterization with ultra-low volume fractions of ~10 –10 is feasible with SAXS. Our technique opens up a doorway to the in-situ analysis of aerosol nanoparticles under atmospheric conditions.

The amounts of halothane and isoflurane trapped after exposure for up to 3 h at 2 MAC in commonly used anaesthesia circuit tubing were quantitated by gas chromatography. The decontaminating effects of procedures such as flushing with oxygen, thermal disinfection and/or routine storage were assessed in a similar way. After halothane exposure, anaesthetic content was highest in silicone (398 +/- 55 mg 100 g-1). Lower quantities were found in all other tubings investigated (electrically conductive latex: 64 +/- 4, conductive rubber: 62 +/- 4, polyethylene-vinyl-acetate (PEVA): 293 +/- 10 and 149 +/- 17 for non-conductive corrugated and spiral tubes, respectively, polysulfone (Hytrel): 155 +/- 10 mg 100 g-1). The isoflurane contents were substantially lower (silicone: 278 +/- 23; others: 55 +/- 7, 61 +/- 6, 163 +/- 9 and 86 +/- 8, 74 +/- 4 mg 100 g-1). The tubings' content did not correlate with the material's partition coefficient as full saturation was not achieved during exposure. Decontamination procedures reduced the content of volatile anaesthetics to a variable extent. Conductive latex and rubber showed the highest residual content, even after thermal disinfection and subsequent storage. Twenty-minute flushing with oxygen (8 l min-1) decreased effluent gas concentrations below 5 p.p.m. in all tubings. With silicone, after 1 h flushing, halothane concentrations still exceeded 10 p.p.m. (isoflurane: 8 p.p.m.). It is concluded that urgent decontamination by a 20-min flush warrants the safe re-use of previously 'contaminated' conductive rubber and latex as well as polysulfone tubings in critical situations, e.g. in malignant hyperthermia patients if disposable tubing is not immediately available.(ABSTRACT TRUNCATED AT 250 WORDS)

Abstract. In this study the impact of humidity on heterogeneous nucleation of n-butanol onto hygroscopic and nonabsorbent particles was investigated using a fast expansion chamber and commercial continuous flow type condensation particle counters (CPCs). More specifically, we measured the activation probability of sodium chloride (NaCl) and silver (Ag) nano-particles by using n-butanol as condensing liquid with the size analyzing nuclei counter (SANC). In addition, the cut-off diameter of regular butanol based CPCs for both seed materials was measured and compared to SANC results. Our findings reveal a strong humidity dependence of NaCl particles in the sub-10 nm size range since the activation of sodium chloride seeds is enhanced with increasing relative humidity. For Ag seeds this humidity dependence was not observed, underlining the importance of molecular interactions between seed and vapor molecules. Consequently, the cut-off diameter of a butanol based CPC can be reduced significantly by increasing the relative humidity. This finding suggests that cut-off diameters of butanol CPCs under ambient conditions are likely smaller than corresponding cut-off diameters measured under clean (dry) laboratory conditions. At the same time, we caution that the humidity dependence may lead to wrong interpretations if the aerosol composition is not known.