In situ observation of synthesized nanoparticles in ultra-dilute aerosols via X-ray scattering

In-air epitaxy of nanostructures (Aerotaxy) has recently emerged as a viable route for fast, large-scale production. In this study, we use small-angle X-ray scattering to perform direct in-flight characterizations of the first step of this process, i.e., the engineered formation of Au and Pt aerosol nanoparticles by spark generation in a flow of N₂ gas. This represents a particular challenge for characterization because the particle density can be extremely low in controlled production. The particles produced are examined during production at operational pressures close to atmospheric conditions and exhibit a lognormal size distribution ranging from 5–100 nm. The Au and Pt particle production and detection are compared. We observe and characterize the nanoparticles at different stages of synthesis and extract the corresponding dominant physical properties, including the average particle diameter and sphericity, as influenced by particle sintering and the presence of aggregates. We observe highly sorted and sintered spherical Au nanoparticles at ultra-dilute concentrations (< 5 × 10⁵ particles/cm³) corresponding to a volume fraction below 3 × 10^–10, which is orders of magnitude below that of previously measured aerosols. We independently confirm an average particle radius of 25 nm via Guinier and Kratky plot analysis. Our study indicates that with high-intensity synchrotron beams and careful consideration of background removal, size and shape information can be obtained for extremely low particle concentrations with industrially relevant narrow size distributions.

     

Methods development for epidemiologic investigations of the health effects of prolonged ozone exposure. Part II. An approach to retrospective estimation of lifetime ozone exposure using a questionnaire and ambient monitoring data (California sites)

An extensive body of data supports a relation between acute exposures to ambient ozone and the occurrence of various acute respiratory symptoms and changes in measures of lung function. In contrast, relatively few data are available on the human health effects that result from long-term exposure to ambient ozone, Current efforts to study long-term ozone-related health effects are limited by the methods available for ascertaining lifetime exposures to ozone. The present feasibility study was undertaken as part of the Health Effects Institute's Environmental Epidemiology Planning Project (Health Effects Institute 1994) to (1) determine whether, in the context of an epidemiologic study, reliable estimates can be obtained for lifetime exposures to ozone by combining estimates from lifetime residential histories, typical activity patterns during life, and residence-specific ambient ozone monitoring data; (2) identify the minimum data required to produce reliable estimates of lifetime exposure; and (3) analyze the relations between various estimates of lifetime ozone exposure and measures of lung function. A convenience sample of 175 first-year students at the University of California, Berkeley, who lived all of their lives in selected areas of California (the Los Angeles Basin or the San Francisco Bay Area), were studied on two occasions (test and retest or test sessions 1 and 2), five to seven days apart. Residential and lifestyle data were obtained from a questionnaire: residence-based ambient ozone exposure values were assigned by interpolation of ambient ozone monitoring data to residential locations. Estimated lifetime exposure was based on average ozone levels between 10 a.m. and 6 p.m. and hours of exposure to ozone concentrations greater than 60 parts per billion (ppb). "Effective" lifetime exposure to ozone was based on a weighted average of estimated time spent in different ambient ozone environments as determined by different combinations of activity data. Pulmonary function was evaluated with flows and volumes from maximum expiratory flow-volume curves and slope of phase III of the single-breath nitrogen washout (SBNW) curves. Although the test-retest reliability of the residential history was acceptably high only for first and second residences, most of the unreliability for other residences came from residences occupied for relatively short durations. Therefore, the test-retest reliability of estimated lifetime exposure to ozone was high, with intraclass correlations greater than 0.90 for all approaches evaluated. Multiple, linear regression analyses showed a consistently negative relation between estimates of lifetime exposure to ozone and flows that reflect the physiology of pulmonary small airways. No relation was observed between lifetime ozone exposure and forced expiratory volume or the slope of phase III, and the relation between lifetime exposure and forced expiratory volume in one second was inconsistent. The results of the flow measures were unaffected by the method used to estimate lifetime exposure and gave effect estimates that were nearly identical. The data from this study indicate that useful and reproducible estimates of lifetime ozone exposure can be obtained in epidemiologic studies by using a residential history. However, the total burden of ozone to which the subjects were exposed cannot be determined accurately from such data. Nonetheless, the estimates so obtained appear to be associated with alterations in pulmonary function that are consistent with the predicted site of maximum effect of ozone in the human lung.     

In situ structure–activity correlation experiments of the ruthenium catalyzed CO oxidation reaction

The complex structure–activity correlation of the CO oxidation on ruthenium has been studied in a batch reactor by using in situ surface X-ray diffraction (SXRD) and on-line mass spectrometry. Two distinct active phases are identified at higher pressures in the mbar range depending on the reaction conditions: a non-oxidic phase and a RuO₂(1 1 0) layer of variable thickness ranging from 1.5 nm to 10 nm. For reaction temperatures lower than 520 K the experimental turnover frequency (TOF) numbers are shown to be almost identical for the two types of active phases. Above 520 K the RuO₂(1 1 0) layer turned out to be much more active than the non-oxidic phase. Kinetic reaction experiments on the RuO₂(1 1 0) phase reveal an activation energy of 78 ± 10 kJ/mol which is in perfect agreement with corresponding reactivity experiments on supported and powder RuO₂ catalyst. Under oxidizing reaction conditions and high concentration of CO₂ in the gas mixture, the RuO₂(1 1 0) model catalyst shows reversible product-poisoning.     

Rice Straw Smoke Generation System for Controlled Human Inhalation Exposures

A unique burner system was designed for the purposes of exposing human subjects to rice straw smoke under highly controlled conditions. The system burns individual straws and has produced particle concentrations up to 900 w g m m 3 in a temperature- and humidity-controlled exposure chamber. Burner operation is fully automatic and programmable. Ignition is by radiant heating in a manner similar to the field. Particle concentration is controlled by the firing interval between straws and by the ratio of burner outlet flow mixing with the main purified air supplied to the exposure chamber. Steady-state particle concentrations are achieved within 5 min from start. Repeatability of particle concentration is excellent at the two exposure levels used, 200 and 500 w g m m 3 . Measurements of particle size distributions suggest that approximately 80% of mass is in the size fraction below 1 w m. Although particle concentrations are controlled at target levels with good precision, emission factors are higher than achieved with similar material in wind tunnel and field experiments. Further characterization of particulate matter is needed to determine if higher emission factors are associated with changes in particle composition and morphology that may influence exposure results.     

Methods development for epidemiologic investigations of the health effects of prolonged ozone exposure. Part I: Variability of pulmonary function measures

The acute and subacute effects of ambient concentrations of ozone on lung function have been studied extensively in a variety of settings. Such studies generally have focused on measures of function that reflect either lung volumes or flows that are influenced by the physiology of large and small airways (e.g., forced expiratory volume in one second [FEV1). Data from animal studies suggest that the effects of prolonged exposure to elevated ambient concentrations of ozone result in abnormalities in the centriacinar region of the lung; and dosimetry models for humans predict that long-term exposure to ozone could impact the same areas of the human lung. However, alterations in structure at this level of the lung are not well reflected by measuring FEV1 until substantial structural changes have occurred. Measures of the lung function that reflect the functional mechanics of airways smaller than 2 mm in diameter are considered to be more relevant. At least one epidemiologic study has provided evidence that small-airway functions may be relevant to effects of prolonged exposure to environments with high concentrations of oxidants. A considerable body of physiologic data has established that flow rates measured during the terminal portion of a maximum expiratory flow-volume (MEFV) curve are largely governed by airways smaller than 2 mm in diameter A similar interpretation has been given to changes in the slope of phase III (delta N2) of the single-breath nitrogen washout (SBNW) curve. Despite the attractiveness of these measures in relation to airway physiology, some data suggest that measurements of flow via the terminal portions of MEFV and SBNW curves have much greater within-subject variability than forced vital capacity (FVC and FEV1. The present study was undertaken as part of a larger feasibility study to develop methods to study the effects of prolonged exposure to elevated ambient ozone levels on lung function in adolescents. A convenience sample of 239 freshmen (ages 16-20 years) entering the University of California, Berkeley were recruited to participate in this protocol. All were lifelong residents of the San Francisco Bay Area or the Los Angeles Basin. Subjects were studied on two occasions five to seven days apart. At each test session, subjects performed up to eight forced expiratory maneuvers to produce three acceptable and reproducible MEFV curves by modified American Thoracic Society criteria. Tests of SBNW were then performed on the basis of detailed criteria for validity and reproducibility. Eight attempts to generate three curves were allowed. The delta N2 was obtained by a least-squares regression of nitrogen concentrations between the 750-mL and 1750-mL volume points. Instantaneous flow at 75% of expired volume (FEF75%), average flow between the 25% and 75% volume points (FEF25%-75%), and delta N2 were the principal outcomes. Variance components were estimated with a nested random effects model with adjustments for important covariates. The average within-subject coefficients of variation (+/-SD of distribution of means) for male subjects were: FEV1 1.2 (+/-0.8); FEF25%-75% 3.2 (+/-2.3); FEF75% 5.8 (+/-5.0); and delta N2 17.9 (+/-12.3); for female subjects they were: FEV1 1.4 (+/-0.9); FEF25%-75% 3.0 (+/-2.2); FEF75% 6.2 (+/-5.2); and delta N2 19.9 (+/-17.0). The variance attributed to test session was less than 1% for all measures. The percentages of variance due to within-subject variation for each measure (adjusted for sex, area of residence, ethnicity, and height) were: FVC 3.6%; FEV1 3.0%; FEF25%-75% 5.2%; FEF75% 8.9%; and delta N2 23.9%. Of all subjects tested, 234 (97.9%) could provide at least two acceptable MEFV curves, but only 218 (91.2%) could provide at least two acceptable SBNW curves. The results were unchanged by recent history of acute, respiratory illness.(ABSTRACT TRUNCATED)     

Self-healing and self-organized gold nanoparticle films at a water/organic solvent interface

Gold nanoparticles (5 nm and 20 nm) have been synthesized and stabilized with mercaptoundecanol. These particles, although insoluble in water or common organic solvents, spread as a thin film at the liquid-liquid interface between a water phase and an organic phase. Films of these gold nanoparticles have been observed both by conventional transmission electron microscopy of deposited samples and by cryo-transmission electron microscopy of plunge-frozen samples. The film can be monolayered and extend over centimeter-sized areas. The particle films spontaneously re-assemble and self-organize at the interface when disrupted. This self-healing capacity of the film should make it possible to build a device for continuous production and deposition of the film.     

The ID03 surface diffraction beamline for in-situ and real-time X-ray investigations of catalytic reactions at surfaces

In this article, we present the current capabilities of the ID03 surface diffraction beamline for the characterisation of catalytic surfaces under reaction. The weak interaction of X-rays with matter makes it possible to design reactor set-ups which can sustain high temperatures and atmospheric pressures while probing the sample reactivity, structure and morphology with surface sensitive X-ray techniques. A few examples are presented as an illustration of the current capabilities.     

Structure and catalytic reactivity of Rh oxides

Using a combination of experimental and theoretical techniques, we show that a thin RhO₂ surface oxide film forms prior to the bulk Rh₂O₃ corundum oxide on all close-packed single crystal Rh surfaces. Based on previous reports, we argue that the RhO₂ surface oxide also forms on vicinal Rh surfaces as well as on Rh nanoparticles. The detailed structure of this film was previously determined using UHV based techniques and density functional theory. In the present paper, we also examine the structure of the bulk Rh₂O₃ corundum oxide using surface X-ray diffraction. Being armed with this structural information, we have explored the CO oxidation reaction over Rh(1 1 1), Rh(1 0 0) and Pt₂₅Rh₇₅(1 0 0) at realistic pressures using in situ surface X-ray diffraction and online mass spectrometry. In all three cases we find that an increase of the CO₂ production coincides with the formation of the thin RhO₂ surface oxide film. In the case of Pt₂₅Rh₇₅(1 0 0), our measurements demonstrate that the formation of bulk Rh₂O₃ corundum oxide poisons the reaction, and argue that this is also valid for all other Rh surfaces. Our study implies that the CO oxidation reaction over Rh surfaces at realistic conditions is insensitive to the exact Rh substrate orientation, but is rather governed by the formation of a specific surface oxide phase.