6 research outputs found
Quantifying shape, size, and composition distributions of nanoparticle aerosols by impaction and electron microscopy
Water vapor inhibits hydrogen sulfide detection in pulsed fluorescence sulfur monitors
The Thermo Scientific 450 Hydrogen Sulfide–Sulfur
Dioxide Analyzer measures
both hydrogen sulfide (H<sub>2</sub>S) and sulfur dioxide (SO<sub>2</sub>). Sulfur dioxide is
measured by pulsed fluorescence, while H<sub>2</sub>S is converted to SO<sub>2</sub> with a
molybdenum catalyst prior to detection. The 450 is widely used to measure
ambient concentrations, e.g., for emissions monitoring and pollution control.
An air stream with a constant H<sub>2</sub>S concentration was generated and the
output of the analyzer recorded as a function of relative humidity (RH). The
analyzer underreported H<sub>2</sub>S as soon as the relative humidity was
increased. The fraction of undetected H<sub>2</sub>S increased from 8.3 at 5.3 %
RH (294 K) to over 34 % at RH  >  80 %. Hydrogen sulfide mole
fractions of 573, 1142, and 5145 ppb were tested. The findings indicate that
previous results obtained with instruments using similar catalysts should be
re-evaluated to correct for interference from water vapor. It is suspected
that water decreases the efficiency of the converter unit and thereby reduces
the measured H<sub>2</sub>S concentration
Fast Brownian Dynamics of Nanoparticles Observed in Liquid Phase Scanning Transmission Electron Microscopy
Treatment of reduced sulphur compounds and SO<sub>2</sub> by Gas Phase Advanced Oxidation
Dip coating of air purifier ceramic honeycombs with photocatalytic TiO<sub>2 </sub>nanoparticles: A case study for occupational exposure
Nanoscale TiO2 (nTiO2) is manufactured in high volumes and is of potential concern in occupational health. Here, we measured workers exposure levels while ceramic honeycombs were dip coated with liquid photoactive nanoparticle suspension and dried with an air blade. The measured nTiO2 concentration levels were used to assess process specific emission rates using a convolution theorem and to calculate inhalation dose rates of deposited nTiO2 particles. Dip coating did not result in detectable release of particles but air blade drying released fine-sized TiO2 and nTiO2 particles. nTiO2 was found in pure nTiO2 agglomerates and as individual particles deposited onto background particles. Total particle emission rates were 420 × 109 min−1, 1.33 × 109 μm2 min−1, and 3.5 mg min−1 respirable mass. During a continued repeated process, the average exposure level was 2.5 × 104 cm−3, 30.3 μm2 cm−3, <116 μg m−3 for particulate matter. The TiO2 average exposure level was 4.2 μg m−3, which is well below the maximum recommended exposure limit of 300 μg m−3 for nTiO2 proposed by the US National Institute for Occupational Safety and Health. During an 8-hour exposure, the observed concentrations would result in a lung deposited surface area of 4.3 × 10−3 cm2 g−1 of lung tissue and 13 μg of TiO2 to the trachea-bronchi, and alveolar regions. The dose levels were well below the one hundredth of the no observed effect level (NOEL1/100) of 0.11 cm2 g−1 for granular biodurable particles and a daily no significant risk dose level of 44 μg day−1. These emission rates can be used in a mass flow model to predict the impact of process emissions on personal and environmental exposure level