Sonic-spray introduction of liquid samples to hand-held Ion mobility spectrometry analyzers.

Sampling hazardous compounds in the form of solids and liquids is a growing need in the fields of homeland security and forensics. Chemical analysis of particles and droplets under field conditions is crucial for various tasks carried out by counter-terrorism and law enforcement units. The use of simple, small and low cost means to achieve this goal is constantly pursued. In this work, an approach for rapid, continuous generation of vapors from liquid samples using sonic spray (SS) as the sample introduction technique, followed by analysis using hand-held ion mobility spectrometry (IMS) vapor analyzers is presented. Transfer of analytes is demonstrated from liquid state to the gas phase at the inlet of an IMS detector using a sonic spray apparatus that consists of a nebulizer, spraying solution, a source of compressed gas and an unheated transfer line tube to the detector inlet nozzle. This technique does not require any electrical, radiative or thermal energy. Analysis of several narcotic substances including cocaine, methamphetamine and amphetamine, and of an explosive compound, TNT, is demonstrated, using two commercial devices as analyzers. Two sampling configurations are presented: direct sampling of liquid, either from a vial or a spill (SS-IMS) and extraction of a substance collected with a swab by dipping it in the spray solvent (ESS-IMS), being suitable for both drops and particles. Limits of detection of the presented method are comparable to those obtained with thermal desorption sample introduction of the commercial device. Time traces of the IMS signals show a continuous and stable signal with a short rise time. This sampling technique may offer competitive performance to that of common thermal desorption techniques, with the advantages of coupling to simpler, smaller and cheaper vapor detectors, optimized for field use, and of a continuous, pulseless sample or object interrogation.

Investigation of the protection efficacy of face shields against aerosol cough droplets.

Simple plastic face shields have numerous practical advantages over regular surgical masks. In light of the spreading COVID-19 pandemic, the potential of face shields as a substitution for surgical masks was investigated. In order to determine the efficacy of the protective equipment we used a cough simulator. The protective equipment considered was placed on a manikin head that simulated human breathing. Concentration and size distribution of small particles that reached the manikin respiration pathways during the few tens of seconds following the cough event were monitored. Additionally, water sensitive papers were taped on the tested protective equipment and the manikin face. In the case of frontal exposure, for droplet diameter larger than 3 µm, the shield efficiency in blocking cough droplets was found to be comparable to that of regular surgical masks, with enhanced protection for portions of the face that the mask does not cover. Additionally, for finer particles, down to 0.3 µm diameter, a shield blocked about 10 times more fine particles than the surgical mask. When exposure from the side was considered, the performance of the shield was found to depend dramatically on its geometry. While a narrow shield allowed more droplets and aerosol to penetrate in comparison to a mask under the same configuration, a slightly wider shield significantly improved the performance. The source control potential of shields was also investigated. A shield, and alternatively, a surgical mask, were placed on the cough simulator, while the breathing simulator, situated 60 cm away in the jet direction, remained totally exposed. In both cases, no droplets or particles were found in the vicinity of the breathing simulator. Conducted experiments were limited to short time periods after expiratory events, and do not include longer time ranges associated with exposure to suspended aerosol. Thus, additional evidence regarding the risk posed by floating aerosol is needed to establish practical conclusions regarding actual transmittance reduction potential of face shields and surgical face masks.

Decontamination of adsorbed chemical warfare agents on activated carbon using hydrogen peroxide solutions.

Mild treatment with hydrogen peroxide solutions (3-30%) efficiently decomposes adsorbed chemical warfare agents (CWAs) on microporous activated carbons used in protective garments and air filters. Better than 95% decomposition of adsorbed sulfur mustard (HD), sarin, and VX was achieved at ambient temperatures within 1-24 h, depending on the H2O2 concentration. HD was oxidized to the nontoxic HD-sulfoxide. The nerve agents were perhydrolyzed to the respective nontoxic methylphosphonic acids. The relative rapidity of the oxidation and perhydrolysis under these conditions is attributed to the microenvironment of the micropores. Apparently, the reactions are favored due to basic sites on the carbon surface. Our findings suggest a potential environmentally friendly route for decontamination of adsorbed CWAs, using H2O2 without the need of cosolvents or activators.