Personal exposure monitoring of PM2.5 among US diplomats in Kathmandu during the COVID-19 lockdown, March to June 2020.

The 2019 Novel Coronavirus SARS-CoV 2 (COVID-191) pandemic has severely impacted global health, safety, economic development and diplomacy. The government of Nepal issued a lockdown order in the Kathmandu Valley for 80 days from 24 March to 11 June 2020. This paper reports associated changes in ambient PM2.5 measured at fixed-site monitors and changes in personal exposure to PM2.5 monitored by APT Minima by four American diplomats who completed monitoring before and during lockdown (24 h for each period per person, 192 person-hours in total). Time activities and use of home air pollution mitigation measures (use of room air cleaners (RACs), sealing of homes) were recorded by standardized diary. We compared PM2.5 exposure level by microenvironment (home (cooking), home (other activities), at work, commuting, other outdoor environment) in terms of averaged PM2.5 concentration and the contribution to cumulative personal exposure (the product of PM2.5 concentration and time spent in each microenvironment). Ambient PM2.5 measured at fixed-sites in the US Embassy and in Phora Durbar were 38.2% and 46.7% lower than during the corresponding period in 2017-2019. The mean concentration of PM2.5 to which US diplomats were exposed was very much lower than the concentrations of ambient levels measured at fixed site monitors in the city both before and during lockdown. Within-person comparisons suggest personal PM2.5 exposure was 50.0% to 76.7% lower during lockdown than before it. Time spent outdoors and cooking at home were large contributors to cumulative personal exposure. Low indoor levels of PM2.5 were achieved at work and home through use of RACs and measures to seal homes against the ingress of polluted air from outside. Our observations indicate the potential reduction in exposure to PM2.5 with large-scale changes to mainly fossil-fuel related emissions sources and through control of indoor environments and activity patterns.

Deployment of networked low-cost sensors and comparison to real-time stationary monitors in New Delhi.

Air quality is a global challenge issue, and many regions of the world, such as India, are experiencing daunting challenges. An important aspect is to identify and then control the emissions from major contributing sources. To advance this aspect, this paper describes an air quality network that has been set up in the National Capital Territory of Delhi (NCT-Delhi) to identify major contributing source categories in real-time. The various components include an innovative cloud-based dashboard to compile the data in real-time from a series of PM instruments (Beta Attenuation Monitors (BAM)) and a low-cost sensor network (22 APT- MAXIMA sensors). Furthermore, at one of the locations (urban site), three real-time chemical speciation monitors are installed to provide elemental speciation (30 elements), elemental carbon (EC), and organic carbon (OC) data. PM2.5 concentrations at different sites (urban, industrial, and background) were compared to the BAM measurements over an 8-month period from May 2019 to February 2020; spanning the summer, monsoon, autumn, and winter seasons in Delhi. The APT sensor measurements were well correlated to the BAM measurements, with R2 values ranging between 0.84 and 0.95 for all sites. This validated that the APT-MAXIMA low-cost sensors can be a useful tool for distributed monitoring of PM2.5 levels. The mean PM2.5 concentrations showed a trend with winter (Dec, Jan, Feb: 205.2 ± 95.1 µg m-3) and autumn (Oct, Nov: 171.7 ± 128.3 µg m-3) highs and summer (May, Jun: 64.6 ± 57.2 µg m-3) and monsoon (Jul, Aug, Sep: 27.6 ± 16.7 µg m-3) lows. The bivariate polar plot reveals high PM2.5 levels originated from local/regional combustion sources located east and south-west of the urban site, especially when high PM2.5 episodes are encountered during the festival season and other smog episodes.Implications: Low-cost sensors are useful for distributed monitoring under both low and high pollution conditions. A cloud-based dashboard system provided real-time, remote access to the data and in the visualization of air quality in the entire region. The real-time data availability on the cloud enabled establishing hot-spot regions of air pollution, spatial variation of PM2.5, real-time source apportionment, and health risk estimates to benefit both policy makers, and the general public.

Non-invasive aerosol delivery and transport of gold nanoparticles to the brain.

Targeted delivery of nanoscale carriers containing packaged payloads to the central nervous system has potential use in many diagnostic and therapeutic applications. Moreover, understanding of the bio-interactions of the engineered nanoparticles used for tissue-specific delivery by non-invasive delivery approaches are also of paramount interest. Here, we have examined this issue systematically in a relatively simple invertebrate model using insects. We synthesized 5 nm, positively charged gold nanoparticles (AuNPs) and targeted their delivery using the electrospray aerosol generator. Our results revealed that after the exposure of synthesized aerosol to the insect antenna, AuNPs reached the brain within an hour. Nanoparticle accumulation in the brain increased linearly with the exposure time. Notably, electrophysiological recordings from neurons in the insect brain several hours after exposure did not show any significant alterations in their spontaneous and odor-evoked spiking properties. Taken together, our findings reveal that aerosolized delivery of nanoparticles can be an effective non-invasive approach for delivering nanoparticles to the brain, and also presents an approach to monitor the short-term nano-biointeractions.

Photochemically assisted fast abiotic oxidation of manganese and formation of δ-MnO2 nanosheets in nitrate solution.

This study introduces a new and previously unconsidered fast abiotic formation of Mn(iv) oxides. We report photochemically assisted fast abiotic oxidation of Mn2+ (aq) to Mn(iv) (s) by superoxide radicals generated from nitrate photolysis. This photochemical pathway generates randomly stacked layered birnessite (δ-MnO2) nanosheets.

Carbon elimination from silicon kerf: Thermogravimetric analysis and mechanistic considerations.

40% of ultrapure silicon is lost as kerf during slicing to produce wafers. Kerf is currently not being recycled due to engineering challenges and costs associated with removing its abundant impurities. Carbon left behind from the lubricant remains as one of the most difficult contaminants to remove in kerf without significant silicon oxidation. The present work enables to better understand the mechanism of carbon elimination in kerf which can aid the design of better processes for kef recycling and low cost photovoltaics. In this paper, we studied the kinetics of carbon elimination from silicon kerf in two atmospheres: air and N2, under a regime of no-diffusion-limitation. We report the apparent activation energy in both atmospheres using three methods: Kissinger, and two isoconversional approaches. In both atmospheres, a bimodal apparent activation energy is observed, suggesting a two stage process. A reaction mechanism is proposed in which (a) C-C and C-O bond cleavage reactions occur in parallel with polymer formation; (b) at higher temperatures, this polymer fully degrades in air but leaves a tarry residue in N2 that accounts for about 12% of the initial total carbon.

Directed assembly of the thylakoid membrane on nanostructured TiO2 for a photo-electrochemical cell.

The thylakoid membrane mainly consists of photosystem I (PSI), photosystem II (PSII) and the cytochrome b6f embedded in a lipid bilayer. PSI and PSII have the ability to capture sunlight and create an electron-hole pair. The study aims at utilizing these properties by using the thylakoid membrane to construct a photo-electrochemical cell. A controlled aerosol technique, electrohydrodynamic atomization, allows a systematic study by the fabrication of different cell configurations based on the surfactant concentration without any linker, sacrificial electron donor and mediator. The maximum photocurrent density observed is 6.7 mA cm(-2) under UV and visible light, and 12 µA cm(-2) under visible light illumination. The electron transfer occurs from PSII to PSI via cytochrome b6f and the electron at PSII is regenerated by water oxidation, similar to the z-scheme of photosynthesis. This work shows that re-engineering the natural photosynthesis circuit by the novel technique of electrospray deposition can result in an environmentally friendly method of harvesting sunlight.

Linker-free deposition and adhesion of Photosystem I onto nanostructured TiO2 for biohybrid photoelectrochemical cells.

Photosystem I (PSI) from oxygenic photosynthetic organisms is an attractive sensitizer for nano-biohybrid solar cells as it has a combined light-harvesting and reaction center in one protein complex and operates at a quantum yield close to one in biological systems. Using a linker-free deposition technique enabled by an electrospray system, PSI was coupled to 1-D nanostructured titanium dioxide thin films to fabricate an electrode for a photoelectrochemical cell. After deposition, the surfactant in the PSI aggregate was dissolved in the surfactant-free electrolyte, ensuring that partly hydrophobic PSI was not resuspended and stayed in contact with titanium dioxide. A maximum current density of 4.15 mA cm(-2) was measured after 10 min of electrospray deposition, and this is the highest current density reported so far for PSI-based photoelectrochemical cells. The high current is attributed to 1D nanostructure of titanium dioxide and orientation of the PSI onto the surface, which allows easy transfer of electrons.

Measurement of sub-2 nm clusters of pristine and composite metal oxides during nanomaterial synthesis in flame aerosol reactors.

Measuring stable clusters to understand particle inception will aid the synthesis of well-controlled nanoparticles via gas-phase aerosol routes. Using a Half Mini differential mobility analyzer, the presence of monomers, dimers, trimers, and tetramers was detected for the first time in a flame aerosol reactor during the synthesis of pristine TiO2 and TiO2/SiO2 nanocomposites. Atomic force microscopy confirmed the presence and the size of sub-2 nm clusters. The detection of these clusters elucidated the initial stages of particle formation during combustion synthesis and supported previous hypotheses that collisional growth from stable monomers of metal oxides is the first step of particle growth.

Study of the charge distribution on liposome particles aerosolized by air-jet atomization.

BACKGROUND: Air-jet atomization is a common technique used for the generation of therapeutic aerosols from liposome suspensions for drug delivery to the lungs. Although the technique does not use an electric field, the aerosols generated by this technique are still charged, and this may affect respiratory drug deposition. METHODS: In this study, the charge distribution of liposomes aerosolized by an air-jet atomizer was measured using a tandem differential mobility analyzer (TDMA) technique. The liposomes, composed of a mixture of two amphiphilic lipids and cholesterol, were synthesized by the dehydration-rehydration vesicle method. The effect of the precursor suspension properties, such as medium composition, pH, conductivity, and lipid mass concentration, on the charge distribution of the liposome aerosols was studied. RESULTS AND CONCLUSIONS: Results showed that the atomized liposomes have a bipolar charge distribution, and the number-fraction of charged liposome aerosols was influenced strongly by properties of the precursor solution under investigation. Liposomes synthesized in deionized water were observed to carry much higher charges than those synthesized in phosphate-buffered saline (PBS). Increasing the lipid mass concentration in the precursor suspension resulted in a decrease in the charge on the aerosols. Thus, the precursor suspension properties--composition, pH, and conductivity--can be used to control the magnitude of charge on liposome aerosols and to synthesize engineered liposome particles for the pulmonary delivery of drugs with controlled alveolar deposition and controlled delivery to alveolar macrophages.