Evaluation of PVC and PTFE filters for direct-on-filter crystalline silica quantification by FTIR.

Direct-on-Filter (DoF) analysis of respirable crystalline silica (RCS) by Fourier Transform Infrared (FTIR) spectroscopy is a useful tool for assessing exposure risks. With the RCS exposure limits becoming lower, it is important to characterize and reduce measurement uncertainties. This study systematically evaluated two filter types (i.e., polyvinyl chloride [PVC] and polytetrafluoroethylene [PTFE]) for RCS measurements by DoF FTIR spectroscopy, including the filter-to-filter and day-to-day variability of blank filter FTIR reference spectra, particle deposition patterns, filtration efficiencies, and pressure drops. For PVC filters sampled at a flow rate of 2.5 L/min for 8 h, the RCS limit of detection (LOD) was 7.4 µg/m3 when a designated laboratory reference filter was used to correct the absorption by the filter media. When the spectrum of the pre-sample filter (blank filter before dust sampling) was used for correction, the LOD could be up to 5.9 µg/m3. The PVC absorption increased linearly with reference filter mass, providing a means to correct the absorption differences between the pre-sample and reference filters. For PTFE, the LODs were 12 and 1.2 µg/m3 when a designated laboratory blank or the pre-sample filter spectrum was used for blank correction, respectively, indicating that using the pre-sample blank spectrum will reduce RCS quantification uncertainty. Both filter types exhibited a consistent radially symmetric deposition pattern when particles were collected using 3-piece cassettes, indicating that RCS can be quantified from a single measurement at the filter center. The most penetrating aerodynamic diameters were around 0.1 µm with filtration efficiencies ≥ 98.8% across the measured particle size range with low-pressure drops (0.2-0.3 kPa) at a flow rate of 2.5 L/min. This study concludes that either the PVC or the PTFE filters are suitable for RCS analysis by DoF FTIR, but proper methods are needed to account for the variability of blank absorption among different filters.

Highly efficient hydroxyapatite/TiO2 composites covered by silver halides as E. coli disinfectant under visible light and dark media.

TiO2-based photocatalysts are seen as the most common agents for the photodegradation of bacteria. In this study, AgCl/TiO2, hydroxyapatite(Hp)/AgCl/TiO2, AgI/TiO2, and Hp/AgI/TiO2 were prepared by the deposition-precipitation method on P25 TiO2 nanoparticles and were characterized by XRD, SEM, FT-IR, EDX and BET methods. The prepared composites showed high efficiency for the inactivation of Escherichia coli (E. coli) bacteria under visible light and in dark media with different catalyst amounts of 12 and 24 mg, respectively. In less than 30 min, AgI/TiO2, prepared by the combination of cationic surfactant and PVPI2, disinfected 1 × 10(7) colony-forming units of E. coli completely. However, AgCl/TiO2 was not stable under the same conditions. Hp was added to AgCl/TiO2 and AgI/TiO2 to extend the antibacterial effect to dark media. Hp/AgCl/TiO2 showed desirable disinfection capabilities under visible light irradiations that function in less than 30 min. During the time interval when the inactivation was complete, the photocatalytic activity of Hp/AgCl/TiO2 under visible light was maintained effectively without the destruction of AgCl. Hp/AgCl/TiO2 and Hp/AgI/TiO2 were found to prevent bacteria from growing during 3 h in the dark. The antibacterial properties of Hp composites in dark environments are mainly due to the strong linkage between Hp and the cell wall which limits the nourishment of bacteria, while under visible light, in addition to the photocatalytic process, the sense-shoot phenomena and the adsorption effects can be accepted.

Bacteriostatic Effects of Apatite-Covered Ag/AgBr/TiO2 Nanocomposite in the Dark: Anomaly in Bacterial Motility.

In this paper, we report a unique property of inactivating Gram-positive/negative bacteria in the dark via apatite-covered Ag/AgBr/TiO2 nanocomposites (AAAT). We demonstrate that the inactivation mechanism is bacteriostatic based on the cellular integrity and motility of bacteria, low toxicity and high durability of AAAT. From straight observations, the catalytic loading affects the bacterial replication and cell envelope as well as inducing an anomaly in bacterial motility (continuous rotation) for both types of bacteria. Both simulation and experimental analyses suggest that the anomaly could be due to posterior intracellular signals rather than purely mechanical effects (e.g., size enlargement and motility retardation). Provoked by chemomechanical stimuli, these signals increase the frequency of flagellar tumbling and eventually entangle the bacteria.